-
1
-
-
38749140677
-
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene
-
Alarcón, M., Abrahams, B. S., Stone, J. L., Duvall, J. A., Perederiy, J. V., Bomar, J. M.,et al. (2008). Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. Am. J. Hum. Genet. 82, 150-159. doi: 10.1016/j.ajhg.2007.09.005
-
(2008)
Am. J. Hum. Genet
, vol.82
, pp. 150-159
-
-
Alarcón, M.1
Abrahams, B.S.2
Stone, J.L.3
Duvall, J.A.4
Perederiy, J.V.5
Bomar, J.M.6
-
2
-
-
14844357203
-
Wnt1 regulates neurogenesis and mediates lateral inhibition of boundary cell specification in the zebrafish hindbrain
-
Amoyel, M., Cheng, Y. C., Jiang, Y. J., and Wilkinson, D. G. (2005). Wnt1 regulates neurogenesis and mediates lateral inhibition of boundary cell specification in the zebrafish hindbrain. Development 132, 775-785. doi: 10.1242/dev.01616
-
(2005)
Development
, vol.132
, pp. 775-785
-
-
Amoyel, M.1
Cheng, Y.C.2
Jiang, Y.J.3
Wilkinson, D.G.4
-
3
-
-
0030841362
-
Mutations of the homeobox genes Dlx-1 and Dlx-2 disrupt the striatal subventricular zone and differentiation of late born striatal neurons
-
Anderson, S. A., Qiu, M., Bulfone, A., Eisenstat, D. D., Meneses, J., Pedersen, R.,et al. (1997). Mutations of the homeobox genes Dlx-1 and Dlx-2 disrupt the striatal subventricular zone and differentiation of late born striatal neurons. Neuron 19, 27-37. doi: 10.1016/S0896-6273(00)80345-1
-
(1997)
Neuron
, vol.19
, pp. 27-37
-
-
Anderson, S.A.1
Qiu, M.2
Bulfone, A.3
Eisenstat, D.D.4
Meneses, J.5
Pedersen, R.6
-
4
-
-
33745604522
-
Robo1 regulates the development of major axon tracts and interneuron migration in the forebrain
-
Andrews, W, Liapi, A, Plachez, C, Camurri, L, Zhang, J, Mori, S., et al. (2006). Robo1 regulates the development of major axon tracts and interneuron migration in the forebrain. Development 133, 2243-2252. doi: 10.1242/dev.02379
-
(2006)
Development
, vol.133
, pp. 2243-2252
-
-
Andrews, W.1
Liapi, A.2
Plachez, C.3
Camurri, L.4
Zhang, J.5
Mori, S.6
-
5
-
-
34247103564
-
NCAM1 association study of bipolar disorder and schizophrenia: polymorphisms and alternatively spliced isoforms lead to similarities and differences
-
Atz, M. E., Rollins, B., and Vawter, M. P. (2007). NCAM1 association study of bipolar disorder and schizophrenia: polymorphisms and alternatively spliced isoforms lead to similarities and differences. Psychiatr. Genet. 17, 55-67. doi: 10.1097/YPG.0b013e328012d850
-
(2007)
Psychiatr. Genet
, vol.17
, pp. 55-67
-
-
Atz, M.E.1
Rollins, B.2
Vawter, M.P.3
-
6
-
-
0037122889
-
Slit proteins prevent midline crossing and determine the dorsoventral position of major axonal pathways in the mammalian forebrain
-
Bagri, A., Marin, O, Plump, A. S., Mak, J., Pleasure, S. J., Rubenstein, L. R.,et al. (2002). Slit proteins prevent midline crossing and determine the dorsoventral position of major axonal pathways in the mammalian forebrain. Neuron 33, 233-248. doi: 10.1016/S0896-6273(02)00561-5
-
(2002)
Neuron
, vol.33
, pp. 233-248
-
-
Bagri, A.1
Marin, O.2
Plump, A.S.3
Mak, J.4
Pleasure, S.J.5
Rubenstein, L.R.6
-
7
-
-
38749099110
-
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders
-
Bakkaloglu, B., O'Roak, B. J., Louvi, A., Gupta, A. R., Abelson, J. F., Morgan, T. M.,et al. (2008). Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders. Am. J. Hum. Genet. 82, 165-173. doi: 10.1016/j.ajhg.2007.09.017
-
(2008)
Am. J. Hum. Genet
, vol.82
, pp. 165-173
-
-
Bakkaloglu, B.1
O'Roak, B.J.2
Louvi, A.3
Gupta, A.R.4
Abelson, J.F.5
Morgan, T.M.6
-
8
-
-
77951576522
-
Drosophila neurexin IV interacts with Roundabout and is required for repulsive midline axon guidance
-
Banerjee, S., Blauth, K., Peters, K., Rogers, S. L., Fanning, A. S., and Bhat, M. A. (2010). Drosophila neurexin IV interacts with Roundabout and is required for repulsive midline axon guidance. J. Neurosci. 30, 5653-5667. doi: 10.1523/JNEUROSCI.6187-09.2010
-
(2010)
J. Neurosci
, vol.30
, pp. 5653-5667
-
-
Banerjee, S.1
Blauth, K.2
Peters, K.3
Rogers, S.L.4
Fanning, A.S.5
Bhat, M.A.6
-
9
-
-
0029075802
-
Expression of zebrafish nk2.2 is influenced by sonic hedgehog/vertebrate hedgehog-1 and demarcates a zone of neuronal differentiation in the embryonic forebrain
-
Barth, K. A., and Wilson, S. W. (1995). Expression of zebrafish nk2.2 is influenced by sonic hedgehog/vertebrate hedgehog-1 and demarcates a zone of neuronal differentiation in the embryonic forebrain. Development 121, 1755-1768.
-
(1995)
Development
, vol.121
, pp. 1755-1768
-
-
Barth, K.A.1
Wilson, S.W.2
-
10
-
-
67650925056
-
Site-specific regulation of cell cycle and DNA repair in post-mitotic GABA cells in schizophrenic versus bipolars
-
Benes, F. M., Lim, B., and Subburaju, S. (2009). Site-specific regulation of cell cycle and DNA repair in post-mitotic GABA cells in schizophrenic versus bipolars. Proc. Natl. Acad. Sci. U.S.A. 106, 11731-11736. doi: 10.1073/pnas.0903066106
-
(2009)
Proc. Natl. Acad. Sci. U.S.A
, vol.106
, pp. 11731-11736
-
-
Benes, F.M.1
Lim, B.2
Subburaju, S.3
-
12
-
-
33644829154
-
Stops along the RAS pathway in human genetic disease
-
Bentires-Alj, M., Kontaridis, M. I., and Neel, B. G. (2006). Stops along the RAS pathway in human genetic disease. Nat. Med. 12, 283-85. doi: 10.1038/nm0306-283
-
(2006)
Nat. Med
, vol.12
, pp. 283-285
-
-
Bentires-Alj, M.1
Kontaridis, M.I.2
Neel, B.G.3
-
13
-
-
84872874456
-
Evolution, brain, and the nature of language
-
Berwick, R. C., Friederici, A., Chomsky, N., and Bolhuis, J. J. (2013). Evolution, brain, and the nature of language. Trends Cogn. Sci. 17, 89-98. doi: 10.1016/j.tics.2012.12.002
-
(2013)
Trends Cogn. Sci
, vol.17
, pp. 89-98
-
-
Berwick, R.C.1
Friederici, A.2
Chomsky, N.3
Bolhuis, J.J.4
-
14
-
-
70350023756
-
CBP/p300 and associated transcriptional co-activators exhibit distinct expression patterns during murine craniofacial and neural tube development
-
Bhattacherjee, V., Horn, K. H., Singh, S., Webb, C. L., Pisano, M. M., and Greene, R. M. (2009). CBP/p300 and associated transcriptional co-activators exhibit distinct expression patterns during murine craniofacial and neural tube development. Int. J. Dev. Biol. 53, 1097-1104. doi: 10.1387/ijdb.072489vb
-
(2009)
Int. J. Dev. Biol
, vol.53
, pp. 1097-1104
-
-
Bhattacherjee, V.1
Horn, K.H.2
Singh, S.3
Webb, C.L.4
Pisano, M.M.5
Greene, R.M.6
-
15
-
-
79952746648
-
Slit2 activity in the migration of guidepost neurons shapes thalamic projections during development and evolution
-
Bielle, F., Marcos-Mondéjar, P., Keita, M., Mailhes, C., Verney, C., Nguyen Ba-Charvet, K.,et al. (2011). Slit2 activity in the migration of guidepost neurons shapes thalamic projections during development and evolution. Neuron 69, 1085-1098. doi: 10.1016/j.neuron.2011.02.026
-
(2011)
Neuron
, vol.69
, pp. 1085-1098
-
-
Bielle, F.1
Marcos-Mondéjar, P.2
Keita, M.3
Mailhes, C.4
Verney, C.5
Nguyen Ba-Charvet, K.6
-
16
-
-
84876561665
-
Age-related cognitive impairments in mice with a conditional ablation of the neural cell adhesion molecule
-
Bisaz, R., Boadas-Vaello, P., Genoux, D., and Sandi, C. (2013). Age-related cognitive impairments in mice with a conditional ablation of the neural cell adhesion molecule. Learn. Mem. 20, 183-193. doi: 10.1101/lm.030064.112
-
(2013)
Learn. Mem
, vol.20
, pp. 183-193
-
-
Bisaz, R.1
Boadas-Vaello, P.2
Genoux, D.3
Sandi, C.4
-
17
-
-
84899704752
-
The shape of the language-ready brain
-
Boeckx, C., and Benítez-Burraco, A. (2014). The shape of the language-ready brain. Front. Psychol. 5:282. doi: 10.3389/fpsyg.2014.00282
-
(2014)
Front. Psychol
, vol.5
, pp. 282
-
-
Boeckx, C.1
Benítez-Burraco, A.2
-
18
-
-
84906272675
-
The functional neuroanatomy of serial order in language
-
Boeckx, C., Martínez-álvarez, A., and Leivada, E. (2014). The functional neuroanatomy of serial order in language. J. Neurolinguist. 32, 1-15. doi: 10.1016/j.jneuroling.2014.07.001
-
(2014)
J. Neurolinguist
, vol.32
, pp. 1-15
-
-
Boeckx, C.1
Martínez-álvarez, A.2
Leivada, E.3
-
19
-
-
84867710614
-
Slit/Robo signaling modulates the proliferation of central nervous system progenitors
-
Borrell, V., Cárdenas, A., Ciceri, G., Galcerán, J., Flames, N., Pla, R.,et al. (2012). Slit/Robo signaling modulates the proliferation of central nervous system progenitors. Neuron 76, 338-352. doi: 10.1016/j.neuron.2012.08.003
-
(2012)
Neuron
, vol.76
, pp. 338-352
-
-
Borrell, V.1
Cárdenas, A.2
Ciceri, G.3
Galcerán, J.4
Flames, N.5
Pla, R.6
-
20
-
-
0242489171
-
A requirement for the immediate early gene zif268 in reconsolidation of recognition memory after retrieval
-
Bozon, B., Davis, S., and Laroche, S. (2003). A requirement for the immediate early gene zif268 in reconsolidation of recognition memory after retrieval. Neuron 40, 695-701. doi: 10.1016/S0896-6273(03)00674-3
-
(2003)
Neuron
, vol.40
, pp. 695-701
-
-
Bozon, B.1
Davis, S.2
Laroche, S.3
-
21
-
-
69449102804
-
Slits are chemorepellents endogenous to hypothalamus and steer thalamocortical axons into ventral telencephalon
-
Braisted, J. E., Ringstedt, T., and O'Leary, D. D. M. (2009). Slits are chemorepellents endogenous to hypothalamus and steer thalamocortical axons into ventral telencephalon. Cereb. Cortex 19, i144-i151. doi: 10.1093/cercor/bhp035
-
(2009)
Cereb. Cortex
, vol.19
, pp. i144-i151
-
-
Braisted, J.E.1
Ringstedt, T.2
O'Leary, D.D.M.3
-
22
-
-
79958240859
-
Transgenic mice overexpressing the extracellular domain of NCAM are impaired in working memory and cortical plasticity
-
Brennaman, L. H., Kochlamazashvili, G., Stoenica, L., Nonneman, R. J., Moy, S. S., Schachner, M.,et al. (2011). Transgenic mice overexpressing the extracellular domain of NCAM are impaired in working memory and cortical plasticity. Neurobiol. Dis. 43, 372-378. doi: 10.1016/j.nbd.2011.04.008
-
(2011)
Neurobiol. Dis
, vol.43
, pp. 372-378
-
-
Brennaman, L.H.1
Kochlamazashvili, G.2
Stoenica, L.3
Nonneman, R.J.4
Moy, S.S.5
Schachner, M.6
-
23
-
-
0035879684
-
Molecular organization of the nodal region is not altered in spontaneously diabetic BB-Wistar rats
-
Brown, A. A., Xu, T., Arroyo, E. J., Levinson, S. R., Brophy, P. J., Peles, E.,et al. (2001). Molecular organization of the nodal region is not altered in spontaneously diabetic BB-Wistar rats. J. Neurosci. Res. 65, 139-149. doi: 10.1002/jnr.1137
-
(2001)
J. Neurosci. Res
, vol.65
, pp. 139-149
-
-
Brown, A.A.1
Xu, T.2
Arroyo, E.J.3
Levinson, S.R.4
Brophy, P.J.5
Peles, E.6
-
24
-
-
84888872635
-
The evolution of distributed association networks in the human brain
-
Buckner, R. L., and Krienen, F. M. (2013). The evolution of distributed association networks in the human brain. Trends Cogn. Sci. 17, 648-665. doi: 10.1016/j.tics.2013.09.017
-
(2013)
Trends Cogn. Sci
, vol.17
, pp. 648-665
-
-
Buckner, R.L.1
Krienen, F.M.2
-
25
-
-
84859361784
-
Pinceau organization in the cerebellum requires distinct functions of neurofascin in Purkinje and basket neurons during postnatal development
-
Buttermore, E. D., Piochon, C., Wallace, M. L., Philpot, B. D., Hansel, C., and Bhat, M. A. (2012). Pinceau organization in the cerebellum requires distinct functions of neurofascin in Purkinje and basket neurons during postnatal development. J. Neurosci. 32, 4724-4742. doi: 10.1523/JNEUROSCI.5602-11.2012
-
(2012)
J. Neurosci
, vol.32
, pp. 4724-4742
-
-
Buttermore, E.D.1
Piochon, C.2
Wallace, M.L.3
Philpot, B.D.4
Hansel, C.5
Bhat, M.A.6
-
26
-
-
34250812575
-
Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly.
-
Buxbaum, J. D., Cai, G., Chaste, P., Nygren, G., Goldsmith, J., Reichert, J.,et al. (2007). Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly. Am. J. Med. Genet. B Neuropsychiatr. Genet. 144B, 484-491. doi: 10.1002/ajmg.b.30493
-
(2007)
Am. J. Med. Genet. B Neuropsychiatr. Genet.
, vol.144 B
, pp. 484-491
-
-
Buxbaum, J.D.1
Cai, G.2
Chaste, P.3
Nygren, G.4
Goldsmith, J.5
Reichert, J.6
-
27
-
-
34547126793
-
Neurotrophin/Trk receptor signaling mediates C/EBPa, -ß and NeuroD recruitment to immediate-early gene promoters in neuronal cells and requires C/EBPs to induce immediate-early gene transcription
-
Calella, A. M., Nerlov, C., Lopez, R. G., Sciarretta, C., von Bohlen und Halbach, O., Bereshchenko, O.,et al. (2007). Neurotrophin/Trk receptor signaling mediates C/EBPa, -ß and NeuroD recruitment to immediate-early gene promoters in neuronal cells and requires C/EBPs to induce immediate-early gene transcription. Neural Dev. 2:4. doi: 10.1186/1749-8104-2-4
-
(2007)
Neural Dev
, vol.2
, pp. 4
-
-
Calella, A.M.1
Nerlov, C.2
Lopez, R.G.3
Sciarretta, C.4
Von Bohlen Und Halbach, O.5
Bereshchenko, O.6
-
28
-
-
0033027914
-
Mash1 regulates neurogenesis in the ventral telencephalon
-
Casarosa, S., Fode, C., and Guillemot, F. (1999). Mash1 regulates neurogenesis in the ventral telencephalon. Development 126, 525-534.
-
(1999)
Development
, vol.126
, pp. 525-534
-
-
Casarosa, S.1
Fode, C.2
Guillemot, F.3
-
29
-
-
84899881782
-
Patterns of coding variation in the complete exomes of three Neandertals
-
Castellano, S., Parra, G., Sánchez-Quinto, F. A., Racimo, F., Kuhlwilm, M., Kircher, M.,et al. (2014). Patterns of coding variation in the complete exomes of three Neandertals. Proc. Natl. Acad. Sci. U.S.A. 111, 6666-6671. doi: 10.1073/pnas.1405138111
-
(2014)
Proc. Natl. Acad. Sci. U.S.A
, vol.111
, pp. 6666-6671
-
-
Castellano, S.1
Parra, G.2
Sánchez-Quinto, F.A.3
Racimo, F.4
Kuhlwilm, M.5
Kircher, M.6
-
30
-
-
84866389516
-
Activation of Robo1 signaling of breast cancer cells by Slit2 from stromal fibroblast restrains tumorigenesis via blocking PI3K/Akt/ß-catenin pathway
-
Chang, P. H., Hwang-Verslues, W. W., Chang, Y. C., Chen, C. C., Hsiao, M., Jeng, Y. M.,et al. (2012). Activation of Robo1 signaling of breast cancer cells by Slit2 from stromal fibroblast restrains tumorigenesis via blocking PI3K/Akt/ß-catenin pathway. Cancer Res. 72, 4652-4661. doi: 10.1158/0008-5472.CAN-12-0877
-
(2012)
Cancer Res
, vol.72
, pp. 4652-4661
-
-
Chang, P.H.1
Hwang-Verslues, W.W.2
Chang, Y.C.3
Chen, C.C.4
Hsiao, M.5
Jeng, Y.M.6
-
31
-
-
84870031935
-
Gbx2 regulates thalamocortical axon guidance by modifying the LIM and Robo codes
-
Chatterjee, M., Li, K., Chen, L., Maisano, X., Guo, Q., Gan, L.,et al. (2012). Gbx2 regulates thalamocortical axon guidance by modifying the LIM and Robo codes. Development 139, 4633-4643. doi: 10.1242/dev.086991
-
(2012)
Development
, vol.139
, pp. 4633-4643
-
-
Chatterjee, M.1
Li, K.2
Chen, L.3
Maisano, X.4
Guo, Q.5
Gan, L.6
-
32
-
-
0035282797
-
The N-terminal leucine-rich regions in slit are sufficient to repel olfactory bulb axons and subventricular zone neurons
-
Chen, J.-H, Wen, L., Dupuis, S., Wu, J. Y., and Rao, Y. (2001). The N-terminal leucine-rich regions in slit are sufficient to repel olfactory bulb axons and subventricular zone neurons. J. Neurosci. 21, 1548-1556.
-
(2001)
J. Neurosci.
, vol.21
, pp. 1548-1556
-
-
Chen J.-H Wen, L.1
Dupuis, S.2
Wu, J.Y.3
Rao, Y.4
-
33
-
-
33646765383
-
Protein kinase Cd-mediated proteasomal degradation of MAP kinase phosphatase-1 contributes to glutamate-induced neuronal cell death
-
Choi, B. H., Hur, E. M., Lee, J. H., Jun, D. J., and Kim, K. T. (2006). Protein kinase Cd-mediated proteasomal degradation of MAP kinase phosphatase-1 contributes to glutamate-induced neuronal cell death. J. Cell. Sci. 119, 1329-1340. doi: 10.1242/jcs.02837
-
(2006)
J. Cell. Sci
, vol.119
, pp. 1329-1340
-
-
Choi, B.H.1
Hur, E.M.2
Lee, J.H.3
Jun, D.J.4
Kim, K.T.5
-
34
-
-
84875779517
-
Role for Lhx2 in corticogenesis through regulation of progenitor differentiation
-
Chou, S. J., and O'Leary, D. D. (2013). Role for Lhx2 in corticogenesis through regulation of progenitor differentiation. Mol. Cell. Neurosci. 56, 1-9. doi: 10.1016/j.mcn.2013.02.006
-
(2013)
Mol. Cell. Neurosci
, vol.56
, pp. 1-9
-
-
Chou, S.J.1
O'Leary, D.D.2
-
35
-
-
84892488334
-
Proteus syndrome review: molecular, clinical, and pathologic features
-
Cohen, M. M. Jr. (2014). Proteus syndrome review: molecular, clinical, and pathologic features. Clin. Genet. 85, 111-119. doi: 10.1111/cge.12266
-
(2014)
Clin. Genet
, vol.85
, pp. 111-119
-
-
Cohen, M.M.1
-
36
-
-
67349235273
-
Developmental regulation of neural cell adhesion molecule in human prefrontal cortex
-
Cox, E. T., Brennaman, L. H., Gable, K. L., Hamer, R. M., Glantz, L. A., Lamantia, A. S.,et al. (2009). Developmental regulation of neural cell adhesion molecule in human prefrontal cortex. Neuroscience 162, 96-105. doi: 10.1016/j.neuroscience.2009.04.037
-
(2009)
Neuroscience
, vol.162
, pp. 96-105
-
-
Cox, E.T.1
Brennaman, L.H.2
Gable, K.L.3
Hamer, R.M.4
Glantz, L.A.5
Lamantia, A.S.6
-
37
-
-
84887119684
-
The XY gene hypothesis of psychosis: origins and current status
-
Crow, T. J. (2013). The XY gene hypothesis of psychosis: origins and current status. Am. J. Med. Genet. B Neuropsychiatr. Genet. 162, 800-824. doi: 10.1002/ajmg.b.32202
-
(2013)
Am. J. Med. Genet. B Neuropsychiatr. Genet
, vol.162
, pp. 800-824
-
-
Crow, T.J.1
-
38
-
-
84870288935
-
RUNX3, EGR1 and SOX9B form a regulatory cascade required to modulate BMP-signaling during cranial cartilage development in zebrafish.
-
Dalcq, J., Pasque, V., Ghaye, A., Larbuisson, A., Motte, P., Martial, J. A.,et al. (2012). RUNX3, EGR1 and SOX9B form a regulatory cascade required to modulate BMP-signaling during cranial cartilage development in zebrafish. PLoS ONE 7:e50140. doi: 10.1371/journal.pone.0050140
-
(2012)
PLoS ONE
, vol.7
-
-
Dalcq, J.1
Pasque, V.2
Ghaye, A.3
Larbuisson, A.4
Motte, P.5
Martial, J.A.6
-
41
-
-
0037743572
-
Neurexin mediates the assembly of presynaptic terminals
-
Dean, C., Scholl, F. G., Choih, J., DeMaria, S., Berger, J., Isacoff, E.,et al. (2003). Neurexin mediates the assembly of presynaptic terminals. Nat. Neurosci. 6, 708-716. doi: 10.1038/nn1074
-
(2003)
Nat. Neurosci
, vol.6
, pp. 708-716
-
-
Dean, C.1
Scholl, F.G.2
Choih, J.3
DeMaria, S.4
Berger, J.5
Isacoff, E.6
-
42
-
-
10744226332
-
Variable phenotype in Greig cephalopolysyndactyly syndrome: clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutations.
-
Debeer, P., Peeters, H., Driess, S., De Smet, L., Freese, K., Matthijs, G.,et al. (2003). Variable phenotype in Greig cephalopolysyndactyly syndrome: clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutations. Am. J. Med. Genet. 120A, 49-58. doi: 10.1002/ajmg.a.20018
-
(2003)
Am. J. Med. Genet.
, vol.120 A
, pp. 49-58
-
-
Debeer, P.1
Peeters, H.2
Driess, S.3
De Smet, L.4
Freese, K.5
Matthijs, G.6
-
43
-
-
84885356685
-
On the antiquity of language: the reinterpretation of Neandertal linguistic capacities and its consequences
-
Dediu, D., and Levinson, S. C. (2013). On the antiquity of language: the reinterpretation of Neandertal linguistic capacities and its consequences. Front. Psychol. 4:397. doi: 10.3389/fpsyg.2013.00397
-
(2013)
Front. Psychol
, vol.4
, pp. 397
-
-
Dediu, D.1
Levinson, S.C.2
-
44
-
-
84890146832
-
APC/C-Cdh1 coordinates neurogenesis and cortical size during development
-
Delgado-Esteban, M., García-Higuera, I., Maestre, C., Moreno, S., and Almeida, A. (2013). APC/C-Cdh1 coordinates neurogenesis and cortical size during development. Nat. Commun. 4:2879. doi: 10.1038/ncomms3879
-
(2013)
Nat. Commun
, vol.4
, pp. 2879
-
-
Delgado-Esteban, M.1
García-Higuera, I.2
Maestre, C.3
Moreno, S.4
Almeida, A.5
-
45
-
-
84907580732
-
FOXP2 drives neuronal differentiation by interacting with retinoic acid signaling pathways
-
Devanna, P., Middelbeek, J., and Vernes, S. C. (2014). FOXP2 drives neuronal differentiation by interacting with retinoic acid signaling pathways. Front. Cell Neurosci. 8:305. doi: 10.3389/fncel.2014.00305
-
(2014)
Front. Cell Neurosci
, vol.8
, pp. 305
-
-
Devanna, P.1
Middelbeek, J.2
Vernes, S.C.3
-
46
-
-
37349032981
-
Robo-Slit interactions regulate longitudinal axon pathfinding in the embryonic vertebrate brain
-
Devine, C. A., and Key, B. (2008). Robo-Slit interactions regulate longitudinal axon pathfinding in the embryonic vertebrate brain. Dev. Biol. 313, 371-383. doi: 10.1016/j.ydbio.2007.10.040
-
(2008)
Dev. Biol
, vol.313
, pp. 371-383
-
-
Devine, C.A.1
Key, B.2
-
48
-
-
34147183677
-
Light-inducible and clock-controlled expression of MAP kinase phosphatase 1 in mouse central pacemaker neurons
-
Doi, M., Cho, S., Yujnovsky, I., Hirayama, J., Cermakian, N., Cato, A. C.,et al. (2007). Light-inducible and clock-controlled expression of MAP kinase phosphatase 1 in mouse central pacemaker neurons. J. Biol. Rhythms 22, 127-139. doi: 10.1177/0748730406298332
-
(2007)
J. Biol. Rhythms
, vol.22
, pp. 127-139
-
-
Doi, M.1
Cho, S.2
Yujnovsky, I.3
Hirayama, J.4
Cermakian, N.5
Cato, A.C.6
-
49
-
-
0031053586
-
Regulation of neuronal survival by the serine-threonine protein kinase Akt
-
Dudek, H., Datta, S. R., Franke, T. F., Birnbaum, M. J., Yao, R., Cooper, G. M.,et al. (1997). Regulation of neuronal survival by the serine-threonine protein kinase Akt. Science 275, 661-665. doi: 10.1126/science.275.5300.661
-
(1997)
Science
, vol.275
, pp. 661-665
-
-
Dudek, H.1
Datta, S.R.2
Franke, T.F.3
Birnbaum, M.J.4
Yao, R.5
Cooper, G.M.6
-
50
-
-
78650924310
-
Midbrain dopaminergic axons are guided longitudinally through the diencephalon by Slit/Robo signals
-
Dugan, J. P., Stratton, A., Riley, H. P., Farmer, W. T., and Mastick, G. S. (2011). Midbrain dopaminergic axons are guided longitudinally through the diencephalon by Slit/Robo signals. Mol. Cell. Neurosci. 46, 347-356. doi: 10.1016/j.mcn.2010.11.003
-
(2011)
Mol. Cell. Neurosci
, vol.46
, pp. 347-356
-
-
Dugan, J.P.1
Stratton, A.2
Riley, H.P.3
Farmer, W.T.4
Mastick, G.S.5
-
52
-
-
0031895948
-
Mutations of the ATM gene detected in Japanese ataxia-telangiectasia patients: possible preponderance of the two founder mutations 4612del165 and 7883del5
-
Ejima, Y., and Sasaki, M. S. (1998). Mutations of the ATM gene detected in Japanese ataxia-telangiectasia patients: possible preponderance of the two founder mutations 4612del165 and 7883del5. Hum. Genet. 102, 403-408. doi: 10.1007/s004390050712
-
(1998)
Hum. Genet
, vol.102
, pp. 403-408
-
-
Ejima, Y.1
Sasaki, M.S.2
-
53
-
-
1242319331
-
Decreased phosphorylation of NMDA receptor type 1 at serine 897 in brains of patients with schizophrenia
-
Emamian, E. S., Karayiorgou, M., and Gogos, J. A. (2004). Decreased phosphorylation of NMDA receptor type 1 at serine 897 in brains of patients with schizophrenia. J. Neurosci. 24, 1561-1564. doi: 10.1523/JNEUROSCI.4650-03.2004
-
(2004)
J. Neurosci
, vol.24
, pp. 1561-1564
-
-
Emamian, E.S.1
Karayiorgou, M.2
Gogos, J.A.3
-
54
-
-
46349089821
-
Molecular mapping of movement-associated areas in the avian brain: a motor theory for vocal learning origin.
-
Feenders, G., Liedvogel, M., Rivas, M., Zapka, M., Horita, H., Hara, E.,et al. (2008). Molecular mapping of movement-associated areas in the avian brain: a motor theory for vocal learning origin. PLoS ONE 3:e1768. doi: 10.1371/journal.pone.0001768
-
(2008)
PLoS ONE
, vol.3
, pp. e1768
-
-
Feenders, G.1
Liedvogel, M.2
Rivas, M.3
Zapka, M.4
Horita, H.5
Hara, E.6
-
55
-
-
0037467540
-
Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain
-
Ferland, R. J., Cherry, T. J., Preware, P. O., Morrisey, E. E., and Walsh, C. A. (2003). Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain. J. Comp. Neurol. 460, 266-279. doi: 10.1002/cne.10654
-
(2003)
J. Comp. Neurol
, vol.460
, pp. 266-279
-
-
Ferland, R.J.1
Cherry, T.J.2
Preware, P.O.3
Morrisey, E.E.4
Walsh, C.A.5
-
56
-
-
18544365699
-
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia
-
Fisher, S. E., Francks, C., Marlow, A. J., MacPhie, I. L., Newbury, D. F., Cardon, L. R.,et al. (2002). Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. Nat. Genet. 30, 86-91. doi: 10.1038/ng792
-
(2002)
Nat. Genet
, vol.30
, pp. 86-91
-
-
Fisher, S.E.1
Francks, C.2
Marlow, A.J.3
MacPhie, I.L.4
Newbury, D.F.5
Cardon, L.R.6
-
57
-
-
29244467422
-
The eloquent ape: genes, brains and the evolution of language
-
Fisher, S. E., and Marcus, G. F. (2006). The eloquent ape: genes, brains and the evolution of language. Nat. Rev. Genet. 7, 9-20. doi: 10.1038/nrg1747
-
(2006)
Nat. Rev. Genet
, vol.7
, pp. 9-20
-
-
Fisher, S.E.1
Marcus, G.F.2
-
58
-
-
63449102727
-
FOXP2 as a molecular window into speech and language
-
Fisher, S. E., and Scharff, C. (2009). FOXP2 as a molecular window into speech and language. Trends Genet. 25, 166-177. doi: 10.1016/j.tig.2009.03.002
-
(2009)
Trends Genet
, vol.25
, pp. 166-177
-
-
Fisher, S.E.1
Scharff, C.2
-
59
-
-
84924178740
-
-
Cambridge: Cambridge University
-
Fitch, W. T. (2010). The Evolution of Language. Cambridge: Cambridge University doi: 10.1017/CBO9780511817779
-
(2010)
The Evolution of Language.
-
-
Fitch, W.T.1
-
60
-
-
84922181785
-
Birdsong and other animal models for human speech, song, and vocal learning
-
ed. M. Arbib (Harvard: MIT Press)
-
Fitch, W. T., and Jarvis, E. D. (2013). "Birdsong and other animal models for human speech, song, and vocal learning," in Language, Music, and the Brain, ed. M. Arbib (Harvard: MIT Press), 499-539.
-
(2013)
In Language, Music, and the Brain
, pp. 499-539
-
-
Fitch, W.T.1
Jarvis, E.D.2
-
61
-
-
0032422555
-
Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia
-
Fox, J. W., Lamperti, E. D., Eksioglu, Y. Z., Hong, S. E., Feng, Y., Graham, D. A.,et al. (1998). Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia. Neuron 21, 1315-1325. doi: 10.1016/S0896-6273(00)80651-0
-
(1998)
Neuron
, vol.21
, pp. 1315-1325
-
-
Fox, J.W.1
Lamperti, E.D.2
Eksioglu, Y.Z.3
Hong, S.E.4
Feng, Y.5
Graham, D.A.6
-
62
-
-
77953936540
-
Right-handed Neandertals: vindija and beyond
-
Frayer, D. W., Lalueza-Fox, C., Fiore, I., Radovcic, J., and Bondioli, L. (2010). Right-handed Neandertals: vindija and beyond. J. Anthrop. Sci. 88, 113-127.
-
(2010)
J. Anthrop. Sci.
, vol.88
, pp. 113-127
-
-
Frayer, D.W.1
Lalueza-Fox, C.2
Fiore, I.3
Radovcic, J.4
Bondioli, L.5
-
63
-
-
84940434964
-
Molecular and phenotypic abnormalities in individuals with germline heterozygous PTEN mutations and autism.
-
[Epub ahead of print].
-
Frazier, T. W., Embacher, R., Tilot, A. K., Koenig, K., Mester, J., and Eng, C. (2014). Molecular and phenotypic abnormalities in individuals with germline heterozygous PTEN mutations and autism. Mol. Psychiatry doi: 10.1038/mp.2014.125 [Epub ahead of print].
-
(2014)
Mol. Psychiatry
-
-
Frazier, T.W.1
Embacher, R.2
Tilot, A.K.3
Koenig, K.4
Mester, J.5
Eng, C.6
-
64
-
-
84904470753
-
What can mice tell us about Foxp2 function?
-
French, C. A., and Fisher, S. E. (2014). What can mice tell us about Foxp2 function? Curr. Opin. Neurobiol. 28C, 72-79. doi: 10.1016/j.conb.2014.07.003
-
(2014)
Curr. Opin. Neurobiol.
, vol.28 C
, pp. 72-79
-
-
French, C.A.1
Fisher, S.E.2
-
65
-
-
3142707223
-
Runx2 induces osteoblast and chondrocyte differentiation and enhances their migration by coupling with PI3K-Akt signaling
-
Fujita, T., Azuma, Y., Fukuyama, R., Hattori, Y., Yoshida, C., Koida, M.,et al. (2004). Runx2 induces osteoblast and chondrocyte differentiation and enhances their migration by coupling with PI3K-Akt signaling. J. Cell Biol. 166, 85-95. doi: 10.1083/jcb.200401138
-
(2004)
J. Cell Biol
, vol.166
, pp. 85-95
-
-
Fujita, T.1
Azuma, Y.2
Fukuyama, R.3
Hattori, Y.4
Yoshida, C.5
Koida, M.6
-
66
-
-
0034657210
-
An essential role of the neuronal cell adhesion molecule contactin in development of the Xenopus primary sensory system
-
Fujita, N., Saito, R., Watanabe, K., and Nagata, S. (2000). An essential role of the neuronal cell adhesion molecule contactin in development of the Xenopus primary sensory system. Dev. Biol. 221, 308-320. doi: 10.1006/dbio.2000.9692
-
(2000)
Dev. Biol
, vol.221
, pp. 308-320
-
-
Fujita, N.1
Saito, R.2
Watanabe, K.3
Nagata, S.4
-
67
-
-
84892436932
-
Clock upregulates intercellular adhesion molecule-1 expression and promotes mononuclear cells adhesion to endothelial cells
-
Gao, Y., Meng, D., Sun, N., Zhu, Z., Zhao, R., Lu, C.,et al. (2014). Clock upregulates intercellular adhesion molecule-1 expression and promotes mononuclear cells adhesion to endothelial cells. Biochem. Biophys. Res. Commun. 443, 586-591. doi: 10.1016/j.bbrc.2013.12.022
-
(2014)
Biochem. Biophys. Res. Commun
, vol.443
, pp. 586-591
-
-
Gao, Y.1
Meng, D.2
Sun, N.3
Zhu, Z.4
Zhao, R.5
Lu, C.6
-
68
-
-
34548857895
-
Novel RUNX1 isoforms determine the fate of acute myeloid leukemia cells by controlling CD56 expression
-
Gattenloehner, S., Chuvpilo, S., Langebrake, C., Reinhardt, D., Müller-Hermelink, H. K., Serfling, E.,et al. (2007). Novel RUNX1 isoforms determine the fate of acute myeloid leukemia cells by controlling CD56 expression. Blood 110, 2027-2033. doi: 10.1182/blood-2007-02-074203
-
(2007)
Blood
, vol.110
, pp. 2027-2033
-
-
Gattenloehner, S.1
Chuvpilo, S.2
Langebrake, C.3
Reinhardt, D.4
Müller-Hermelink, H.K.5
Serfling, E.6
-
69
-
-
16944364984
-
X-linked situs abnormalities result from mutations in ZIC3
-
Gebbia, M., Ferrero, G. B., Pilia, G., Bassi, M. T., Aylsworth, A. S., Penman-Splitt, M.,et al. (1997). X-linked situs abnormalities result from mutations in ZIC3. Nat. Genet. 17, 305-308. doi: 10.1038/ng1197-305
-
(1997)
Nat. Genet
, vol.17
, pp. 305-308
-
-
Gebbia, M.1
Ferrero, G.B.2
Pilia, G.3
Bassi, M.T.4
Aylsworth, A.S.5
Penman-Splitt, M.6
-
70
-
-
61849112232
-
cAMP enhances BMP2-signaling through PKA and MKP1-dependent mechanisms
-
Ghayor, C., Ehrbar, M., San Miguel, B., Grätz, K. W., and Weber, F. E. (2009). cAMP enhances BMP2-signaling through PKA and MKP1-dependent mechanisms. Biochem. Biophys. Res. Commun. 381, 247-252. doi: 10.1016/j.bbrc.2009.02.032
-
(2009)
Biochem. Biophys. Res. Commun
, vol.381
, pp. 247-252
-
-
Ghayor, C.1
Ehrbar, M.2
San Miguel, B.3
Grätz, K.W.4
Weber, F.E.5
-
71
-
-
0033579430
-
MRG1 binds to the LIM domain of Lhx2 and may function as a coactivator to stimulate glycoprotein hormone alpha-subunit gene expression
-
Glenn, D. J., and Maurer, R. A. (1999). MRG1 binds to the LIM domain of Lhx2 and may function as a coactivator to stimulate glycoprotein hormone alpha-subunit gene expression. J. Biol. Chem. 274, 36159-36167. doi: 10.1074/jbc.274.51.36159
-
(1999)
J. Biol. Chem
, vol.274
, pp. 36159-36167
-
-
Glenn, D.J.1
Maurer, R.A.2
-
72
-
-
42649091463
-
Characterization of the proneural gene regulatory network during mouse telencephalon development
-
Gohlke, J. M., Armant, O., Parham, F. M., Smith, M. V., Zimmer, C., Castro, D. S.,et al. (2008). Characterization of the proneural gene regulatory network during mouse telencephalon development. BMC Biol. 6:15. doi: 10.1186/1741-7007-6-15
-
(2008)
BMC Biol
, vol.6
, pp. 15
-
-
Gohlke, J.M.1
Armant, O.2
Parham, F.M.3
Smith, M.V.4
Zimmer, C.5
Castro, D.S.6
-
73
-
-
84900442346
-
Reconstructing the DNA methylation maps of the Neandertal and the Denisovan
-
Gokhman, D., Lavi, E., Prüfer, K., Fraga, M. F., Riancho, J. A., Kelso, J.,et al. (2014). Reconstructing the DNA methylation maps of the Neandertal and the Denisovan. Science 344, 523-527. doi: 10.1126/science.1250368
-
(2014)
Science
, vol.344
, pp. 523-527
-
-
Gokhman, D.1
Lavi, E.2
Prüfer, K.3
Fraga, M.F.4
Riancho, J.A.5
Kelso, J.6
-
74
-
-
84872857437
-
Decoding the genetics of speech and language
-
Graham, S. A., and Fisher, S. E. (2013). Decoding the genetics of speech and language. Curr. Opin. Neurobiol. 23, 43-51. doi: 10.1016/j.conb.2012.11.006
-
(2013)
Curr. Opin. Neurobiol
, vol.23
, pp. 43-51
-
-
Graham, S.A.1
Fisher, S.E.2
-
75
-
-
84866149000
-
Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene
-
Gras, D., Jonard, L., Roze, E., Chantot-Bastaraud, S., Koht, J., Motte, J.,et al. (2012). Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene. J. Neurol. Neurosurg. Psychiatry 83, 956-962. doi: 10.1136/jnnp-2012-302505
-
(2012)
J. Neurol. Neurosurg. Psychiatry
, vol.83
, pp. 956-962
-
-
Gras, D.1
Jonard, L.2
Roze, E.3
Chantot-Bastaraud, S.4
Koht, J.5
Motte, J.6
-
76
-
-
77952136530
-
A draft sequence of the Neandertal genome
-
Green, R. E., Krause, J., Briggs, A. W., Maricic, T., Stenzel, U., Kircher, M.,et al. (2010). A draft sequence of the Neandertal genome. Science 328, 710-722. doi: 10.1126/science.1188021
-
(2010)
Science
, vol.328
, pp. 710-722
-
-
Green, R.E.1
Krause, J.2
Briggs, A.W.3
Maricic, T.4
Stenzel, U.5
Kircher, M.6
-
77
-
-
79961165354
-
Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1
-
Gregor, A., Albrecht, B., Bader, I., Bijlsma, E. K., Ekici, A. B., Engels, H.,et al. (2011). Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1. BMC Med. Genet. 12:106. doi: 10.1186/1471-2350-12-106
-
(2011)
BMC Med. Genet
, vol.12
, pp. 106
-
-
Gregor, A.1
Albrecht, B.2
Bader, I.3
Bijlsma, E.K.4
Ekici, A.B.5
Engels, H.6
-
78
-
-
0041884720
-
Truncation of C-mip (Tc-mip), a new proximal signaling protein, induces c-maf Th2 transcription factor and cytoskeleton reorganization
-
Grimbert, P., Valanciute, A., Audard, V., Pawlak, A., Le Gouvelo, S., Lang, P.,et al. (2003). Truncation of C-mip (Tc-mip), a new proximal signaling protein, induces c-maf Th2 transcription factor and cytoskeleton reorganization. J. Exp. Med. 198, 797-807. doi: 10.1084/jem.20030566
-
(2003)
J. Exp. Med
, vol.198
, pp. 797-807
-
-
Grimbert, P.1
Valanciute, A.2
Audard, V.3
Pawlak, A.4
Le Gouvelo, S.5
Lang, P.6
-
79
-
-
40149112272
-
Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits
-
Groszer, M., Keays, D. A., Deacon, R. M., de Bono, J. P., Prasad-Mulcare, S., Gaub, S.,et al. (2008). Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits. Curr. Biol. 18, 354-362. doi: 10.1016/j.cub.2008.01.060
-
(2008)
Curr. Biol
, vol.18
, pp. 354-362
-
-
Groszer, M.1
Keays, D.A.2
Deacon, R.M.3
De Bono, J.P.4
Prasad-Mulcare, S.5
Gaub, S.6
-
80
-
-
0031869926
-
The hem of the embryonic cerebral cortex is defined by the expression of multiple Wnt genes and is compromised in Gli3-deficient mice
-
Grove, E. A., Tole, S., Limon, J., Yip, L., and Ragsdale, C. W. (1998). The hem of the embryonic cerebral cortex is defined by the expression of multiple Wnt genes and is compromised in Gli3-deficient mice. Development 125, 2315-2325.
-
(1998)
Development
, vol.125
, pp. 2315-2325
-
-
Grove, E.A.1
Tole, S.2
Limon, J.3
Yip, L.4
Ragsdale, C.W.5
-
81
-
-
0035896580
-
Insulin suppresses transactivation by CAAT/enhancer-binding proteins beta (C/EBPß). Signaling to p300/CREB-binding protein by protein kinase B disrupts interaction with the major activation domain of C/EBPß.
-
Guo, S., Cichy, S. B., He, X., Yang, Q., Ragland, M., Ghosh, A. K.,et al. (2001). Insulin suppresses transactivation by CAAT/enhancer-binding proteins beta (C/EBPß). Signaling to p300/CREB-binding protein by protein kinase B disrupts interaction with the major activation domain of C/EBPß. J. Biol. Chem. 276, 8516-8523. doi: 10.1074/jbc. M008542200
-
(2001)
J. Biol. Chem
, vol.276
, pp. 8516-8523
-
-
Guo, S.1
Cichy, S.B.2
He, X.3
Yang, Q.4
Ragland, M.5
Ghosh, A.K.6
-
82
-
-
0037059765
-
CCAAT/enhancer-binding proteins (C/EBP) ß and d activate osteocalcin gene transcription and synergize with Runx2 at the C/EBP element to regulate bone-specific expression
-
Gutiérrez, S., Javed, A., Tennant, D. K., van Rees, M., Montecino, M., Stein, G. S.,et al. (2002). CCAAT/enhancer-binding proteins (C/EBP) ß and d activate osteocalcin gene transcription and synergize with Runx2 at the C/EBP element to regulate bone-specific expression. J. Biol. Chem. 277, 1316-1323. doi: 10.1074/jbc. M106611200
-
(2002)
J. Biol. Chem
, vol.277
, pp. 1316-1323
-
-
Gutiérrez, S.1
Javed, A.2
Tennant, D.K.3
van Rees, M.4
Montecino, M.5
Stein, G.S.6
-
83
-
-
84874922270
-
ABL1 in thalamus is associated with safety but not fear learning
-
Habib, M. R., Ganea, D. A., Katz, I. K., and Lamprecht, R. (2013). ABL1 in thalamus is associated with safety but not fear learning. Front. Syst. Neurosci. 7:5. doi: 10.3389/fnsys.2013.00005
-
(2013)
Front. Syst. Neurosci
, vol.7
, pp. 5
-
-
Habib, M.R.1
Ganea, D.A.2
Katz, I.K.3
Lamprecht, R.4
-
84
-
-
84862170186
-
Mouse thalamic differentiation: gli-dependent pattern and gli-independent prepattern
-
Haddad-Tóvolli, R., Heide, M., Zhou, X., Blaess, S., and álvarez-Bolado, G. (2012). Mouse thalamic differentiation: gli-dependent pattern and gli-independent prepattern. Front. Neurosci. 6:27. doi: 10.3389/fnins.2012.00027
-
(2012)
Front. Neurosci
, vol.6
, pp. 27
-
-
Haddad-Tóvolli, R.1
Heide, M.2
Zhou, X.3
Blaess, S.4
álvarez-Bolado, G.5
-
85
-
-
1842454166
-
FoxP2 expression in avian vocal learners and non-learners
-
Haesler, S., Wada, K., Nshdejan, A., Morrisey, E. E., Lints, T., Jarvis, E. D.,et al. (2004). FoxP2 expression in avian vocal learners and non-learners. J. Neurosci. 24, 3164-3175. doi: 10.1523/JNEUROSCI.4369-03.2004
-
(2004)
J. Neurosci
, vol.24
, pp. 3164-3175
-
-
Haesler, S.1
Wada, K.2
Nshdejan, A.3
Morrisey, E.E.4
Lints, T.5
Jarvis, E.D.6
-
86
-
-
78249268820
-
De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment
-
Hamdan, F. F., Daoud, H., Rochefort, D., Piton, A., Gauthier, J., Langlois, M.,et al. (2010). De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment. Am. J. Hum. Genet. 87, 671-678. doi: 10.1016/j.ajhg.2010.09.017
-
(2010)
Am. J. Hum. Genet
, vol.87
, pp. 671-678
-
-
Hamdan, F.F.1
Daoud, H.2
Rochefort, D.3
Piton, A.4
Gauthier, J.5
Langlois, M.6
-
87
-
-
84895532455
-
ß-catenin enhances odontoblastic differentiation of dental pulp cells through activation of Runx2.
-
Han, N., Zheng, Y., Li, R., Li, X., Zhou, M., Niu, Y.,et al. (2014). ß-catenin enhances odontoblastic differentiation of dental pulp cells through activation of Runx2. PLoS ONE 9:e88890. doi: 10.1371/journal.pone.0088890
-
(2014)
PLoS ONE
, vol.9
-
-
Han, N.1
Zheng, Y.2
Li, R.3
Li, X.4
Zhou, M.5
Niu, Y.6
-
88
-
-
33745343959
-
The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia.
-
Hannula-Jouppi, K., Kaminen-Ahola, N., Taipale, M., Eklund, R., Nopola-Hemmi, J., Kääriäinen, H.,et al. (2005). The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia. PLoS Genetics 1:e50. doi: 10.1371/journal.pgen.0010050
-
(2005)
PLoS Genetics
, vol.1
, pp. e50
-
-
Hannula-Jouppi, K.1
Kaminen-Ahola, N.2
Taipale, M.3
Eklund, R.4
Nopola-Hemmi, J.5
Kääriäinen, H.6
-
89
-
-
57349084646
-
Signaling mechanisms of neurite outgrowth induced by the cell adhesion molecules NCAM and N-cadherin
-
Hansen, S. M., Berezin, V., and Bock, E. (2008). Signaling mechanisms of neurite outgrowth induced by the cell adhesion molecules NCAM and N-cadherin. Cell Mol. Life Sci. 65, 3809-3821. doi: 10.1007/s00018-008-8290-0
-
(2008)
Cell Mol. Life Sci
, vol.65
, pp. 3809-3821
-
-
Hansen, S.M.1
Berezin, V.2
Bock, E.3
-
90
-
-
84860249365
-
Development and evolution of cerebellar neural circuits
-
Hashimoto, M., and Hibi, M. (2012). Development and evolution of cerebellar neural circuits. Dev. Growth Differ. 54, 373-389. doi: 10.1111/j.1440-169X.2012.01348.x
-
(2012)
Dev. Growth Differ
, vol.54
, pp. 373-389
-
-
Hashimoto, M.1
Hibi, M.2
-
91
-
-
0142026157
-
Differential activities of Sonic hedgehog mediated by Gli transcription factors define distinct neuronal subtypes in the dorsal thalamus
-
Hashimoto-Torii, K., Motoyama, J., Hui, C. C., Kuroiwa, A., Nakafuku, M., and Shimamura, K. (2003). Differential activities of Sonic hedgehog mediated by Gli transcription factors define distinct neuronal subtypes in the dorsal thalamus. Mech. Dev. 120, 1097-1111. doi: 10.1016/j.mod.2003.09.001
-
(2003)
Mech. Dev
, vol.120
, pp. 1097-1111
-
-
Hashimoto-Torii, K.1
Motoyama, J.2
Hui, C.C.3
Kuroiwa, A.4
Nakafuku, M.5
Shimamura, K.6
-
92
-
-
34548346860
-
Promoter regions of many neural- and nutrition-related genes have experienced positive selection during human evolution
-
Haygood, R., Fedrigo, O., Hanson, B., Yokoyama, K. D., and Wray, G. A. (2007). Promoter regions of many neural- and nutrition-related genes have experienced positive selection during human evolution. Nat. Genet. 39, 1140-1144. doi: 10.1038/ng2104
-
(2007)
Nat. Genet
, vol.39
, pp. 1140-1144
-
-
Haygood, R.1
Fedrigo, O.2
Hanson, B.3
Yokoyama, K.D.4
Wray, G.A.5
-
93
-
-
79961186333
-
Structure of p300 bound to MEF2 on DNA reveals a mechanism of enhanceosome assembly
-
He, J., Ye, J., Cai, Y., Riquelme, C., Liu, J. O., Liu, X.,et al. (2011). Structure of p300 bound to MEF2 on DNA reveals a mechanism of enhanceosome assembly. Nucleic Acids Res. 39, 4464-4474. doi: 10.1093/nar/gkr030
-
(2011)
Nucleic Acids Res
, vol.39
, pp. 4464-4474
-
-
He, J.1
Ye, J.2
Cai, Y.3
Riquelme, C.4
Liu, J.O.5
Liu, X.6
-
94
-
-
84883039771
-
Tyrosine kinase inhibition facilitates autophagic SNCA/a-synuclein clearance
-
Hebron, M. L., Lonskaya, I., and Moussa, C. E. (2013). Tyrosine kinase inhibition facilitates autophagic SNCA/a-synuclein clearance. Autophagy 9, 1249-1250. doi: 10.4161/auto.25368
-
(2013)
Autophagy
, vol.9
, pp. 1249-1250
-
-
Hebron, M.L.1
Lonskaya, I.2
Moussa, C.E.3
-
95
-
-
33747772028
-
Rubinstein-Taybi syndrome
-
Hennekam, R. C. (2006). Rubinstein-Taybi syndrome. Eur. J. Hum. Genet. 14, 981-985. doi: 10.1038/sj.ejhg.5201594
-
(2006)
Eur. J. Hum. Genet
, vol.14
, pp. 981-985
-
-
Hennekam, R.C.1
-
96
-
-
84884686593
-
Cavin-3 dictates the balance between ERK and Akt signaling.
-
Hernández, V. J., Weng, J., Ly, P., Pompey, S., Dong, H., Mishra, L.,et al. (2013). Cavin-3 dictates the balance between ERK and Akt signaling. Elife 2:e00905. doi: 10.7554/eLife.00905
-
(2013)
Elife
, vol.2
-
-
Hernández, V.J.1
Weng, J.2
Ly, P.3
Pompey, S.4
Dong, H.5
Mishra, L.6
-
97
-
-
84856039549
-
Computational neuroanatomy of speech production
-
Hickok, G. (2012). Computational neuroanatomy of speech production. Nat. Rev. Neurosci. 13, 135-145. doi: 10.1038/nrn3158
-
(2012)
Nat. Rev. Neurosci
, vol.13
, pp. 135-145
-
-
Hickok, G.1
-
98
-
-
79551659503
-
Sensorimotor integration in speech processing: computational basis and neural organization
-
Hickok, G., Houde, J., and Rong, F. (2011). Sensorimotor integration in speech processing: computational basis and neural organization. Neuron 69, 407-422. doi: 10.1016/j.neuron.2011.01.019
-
(2011)
Neuron
, vol.69
, pp. 407-422
-
-
Hickok, G.1
Houde, J.2
Rong, F.3
-
99
-
-
34247487053
-
The cortical organization of speech processing
-
Hickok, G., and Poeppel, D. (2007). The cortical organization of speech processing. Nat. Rev. Neurosci. 8, 393-402. doi: 10.1038/nrn2113
-
(2007)
Nat. Rev. Neurosci
, vol.8
, pp. 393-402
-
-
Hickok, G.1
Poeppel, D.2
-
100
-
-
33745068650
-
GSK3ß and PKC? function in centrosome localization and process stabilization during Slit-mediated neuronal repolarization
-
Higginbotham, H., Tanaka, T., Brinkman, B. C., and Gleeson, J. G. (2006). GSK3ß and PKC? function in centrosome localization and process stabilization during Slit-mediated neuronal repolarization. Mol. Cell. Neurosci. 32, 118-132. doi: 10.1016/j.mcn.2006.03.003
-
(2006)
Mol. Cell. Neurosci
, vol.32
, pp. 118-132
-
-
Higginbotham, H.1
Tanaka, T.2
Brinkman, B.C.3
Gleeson, J.G.4
-
101
-
-
84856971211
-
C/EBPß and RUNX2 cooperate to degrade cartilage with MMP-13 as the target and HIF-2a as the inducer in chondrocytes
-
Hirata, M., Kugimiya, F., Fukai, A., Saito, T., Yano, F., Ikeda, T.,et al. (2012). C/EBPß and RUNX2 cooperate to degrade cartilage with MMP-13 as the target and HIF-2a as the inducer in chondrocytes. Hum. Mol. Genet. 21, 1111-1123. doi: 10.1093/hmg/ddr540
-
(2012)
Hum. Mol. Genet
, vol.21
, pp. 1111-1123
-
-
Hirata, M.1
Kugimiya, F.2
Fukai, A.3
Saito, T.4
Yano, F.5
Ikeda, T.6
-
102
-
-
84864450280
-
Specialized motor-driven Dusp1 expression in the song systems of multiple lineages of vocal learning birds.
-
Horita, H., Kobayashi, M., Liu, W. C., Oka, K., Jarvis, E. D., and Wada, K. (2012). Specialized motor-driven Dusp1 expression in the song systems of multiple lineages of vocal learning birds. PLoS ONE 7:e42173. doi: 10.1371/journal.pone.0042173
-
(2012)
PLoS ONE
, vol.7
-
-
Horita, H.1
Kobayashi, M.2
Liu, W.C.3
Oka, K.4
Jarvis, E.D.5
Wada, K.6
-
103
-
-
77954576982
-
The dusp1 immediate early gene is regulated by natural stimuli predominantly in sensory input neurons
-
Horita, H., Wada, K., Rivas, M. V., Hara, E., and Jarvis, E. D. (2010). The dusp1 immediate early gene is regulated by natural stimuli predominantly in sensory input neurons. J. Comp. Neurol. 518, 2873-901. doi: 10.1002/cne.22370
-
(2010)
J. Comp. Neurol
, vol.518
, pp. 2873-2901
-
-
Horita, H.1
Wada, K.2
Rivas, M.V.3
Hara, E.4
Jarvis, E.D.5
-
104
-
-
77957896206
-
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits
-
Horn, D., Kapeller, J., Rivera-Brugués, N., Moog, U., Lorenz-Depiereux, B., Eck, S.,et al. (2010). Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. Hum. Mutat. 31, E1851-E1860. doi: 10.1002/humu.21362
-
(2010)
Hum. Mutat
, vol.31
, pp. E1851-E1860
-
-
Horn, D.1
Kapeller, J.2
Rivera-Brugués, N.3
Moog, U.4
Lorenz-Depiereux, B.5
Eck, S.6
-
105
-
-
0033180233
-
Chemorepulsion of neuronal migration by Slit2 in the developing mammalian forebrain
-
Hu, H. (1999). Chemorepulsion of neuronal migration by Slit2 in the developing mammalian forebrain. Neuron 23, 703-711. doi: 10.1016/S0896-6273(01)80029-5
-
(1999)
Neuron
, vol.23
, pp. 703-711
-
-
Hu, H.1
-
106
-
-
84901750757
-
Prospective signs of cleidocranial dysplasia in Cebpb deficiency
-
Huang, B., Takahashi, K., Jennings, E. A., Pumtang-On, P., Kiso, H., Togo, Y.,et al. (2014). Prospective signs of cleidocranial dysplasia in Cebpb deficiency. J. Biomed. Sci. 21:44. doi: 10.1186/1423-0127-21-44
-
(2014)
J. Biomed. Sci
, vol.21
, pp. 44
-
-
Huang, B.1
Takahashi, K.2
Jennings, E.A.3
Pumtang-On, P.4
Kiso, H.5
Togo, Y.6
-
107
-
-
19444377295
-
The neuronal POU transcription factor Brn-2 interacts with Jab1, a gene involved in the onset of neurodegenerative diseases
-
Huang, Y. T., Iwamoto, K., Kurosaki, T., Nasu, M., and Ueda, S. (2005). The neuronal POU transcription factor Brn-2 interacts with Jab1, a gene involved in the onset of neurodegenerative diseases. Neurosci. Lett. 382, 175-178. doi: 10.1016/j.neulet.2005.03.008
-
(2005)
Neurosci. Lett
, vol.382
, pp. 175-178
-
-
Huang, Y.T.1
Iwamoto, K.2
Kurosaki, T.3
Nasu, M.4
Ueda, S.5
-
108
-
-
65249129345
-
Regulation of Cdh1-APC function in axon growth by Cdh1 phosphorylation
-
Huynh, M. A., Stegmüller, J., Litterman, N., and Bonni, A. (2009). Regulation of Cdh1-APC function in axon growth by Cdh1 phosphorylation. J. Neurosci. 29, 4322-4327. doi: 10.1523/JNEUROSCI.5329-08.2009
-
(2009)
J. Neurosci
, vol.29
, pp. 4322-4327
-
-
Huynh, M.A.1
Stegmüller, J.2
Litterman, N.3
Bonni, A.4
-
109
-
-
84864024007
-
Gbx2 directly restricts Otx2 expression to forebrain and midbrain, competing with class III POU factors
-
Inoue, F., Kurokawa, D., Takahashi, M., and Aizawa, S. (2012). Gbx2 directly restricts Otx2 expression to forebrain and midbrain, competing with class III POU factors. Mol. Cell. Biol. 32, 2618-2627. doi: 10.1128/MCB.00083-12
-
(2012)
Mol. Cell. Biol
, vol.32
, pp. 2618-2627
-
-
Inoue, F.1
Kurokawa, D.2
Takahashi, M.3
Aizawa, S.4
-
110
-
-
51249096975
-
Runx transcription factors in neuronal development
-
Inoue, K. I., Shiga, T., and Ito, Y. (2008). Runx transcription factors in neuronal development. Neural Dev. 3, 8104-8103. doi: 10.1186/1749-8104-3-20
-
(2008)
Neural Dev
, vol.3
, pp. 8103-8104
-
-
Inoue, K.I.1
Shiga, T.2
Ito, Y.3
-
111
-
-
84885661377
-
Noncanonical transforming growth factor ß (TGFß) signaling in cranial neural crest cells causes tongue muscle developmental defects
-
Iwata, J., Suzuki, A., Pelikan, R. C., Ho, T. V., and Chai, Y. (2013). Noncanonical transforming growth factor ß (TGFß) signaling in cranial neural crest cells causes tongue muscle developmental defects. J. Biol. Chem. 288, 29760-29770. doi: 10.1074/jbc. M113.493551
-
(2013)
J. Biol. Chem
, vol.288
, pp. 29760-29770
-
-
Iwata, J.1
Suzuki, A.2
Pelikan, R.C.3
Ho, T.V.4
Chai, Y.5
-
112
-
-
3242716663
-
Learned birdsong and the neurobiology of human language
-
Jarvis, E. D. (2004). Learned birdsong and the neurobiology of human language. Ann. N. Y. Acad. Sci. 1016, 749-777. doi: 10.1196/annals.1298.038
-
(2004)
Ann. N. Y. Acad. Sci
, vol.1016
, pp. 749-777
-
-
Jarvis, E.D.1
-
113
-
-
0037040917
-
c-Cbl binding and ubiquitin-dependent lysosomal degradation of membrane-associated Notch1
-
Jehn, B. M., Dittert, I., Beyer, S., von der, M. K., and Bielke, W. (2002). c-Cbl binding and ubiquitin-dependent lysosomal degradation of membrane-associated Notch1. J. Biol. Chem. 277, 8033-8040. doi: 10.1074/jbc. M108552200
-
(2002)
J. Biol. Chem
, vol.277
, pp. 8033-8040
-
-
Jehn, B.M.1
Dittert, I.2
Beyer, S.3
Von Der, M.K.4
Bielke, W.5
-
114
-
-
3142720638
-
Transforming growth factor-beta stimulates p300-dependent RUNX3 acetylation, which inhibits ubiquitination-mediated degradation
-
Jin, Y. H., Jeon, E. J., Li, Q. L., Lee, Y. H., Choi, J. K., Kim, W. J.,et al. (2004). Transforming growth factor-beta stimulates p300-dependent RUNX3 acetylation, which inhibits ubiquitination-mediated degradation. J. Biol. Chem. 279, 29409-29417. doi: 10.1074/jbc. M313120200
-
(2004)
J. Biol. Chem
, vol.279
, pp. 29409-29417
-
-
Jin, Y.H.1
Jeon, E.J.2
Li, Q.L.3
Lee, Y.H.4
Choi, J.K.5
Kim, W.J.6
-
115
-
-
0033536637
-
The tyrosine kinase negative regulator c-Cbl as a RING-type, E2-dependent ubiquitin-protein ligase
-
Joazeiro, C. A. P., Wing, S. S., Huang, H., Leverson, J. D., Hunter, T., and Liu., Y.-C. (1999). The tyrosine kinase negative regulator c-Cbl as a RING-type, E2-dependent ubiquitin-protein ligase. Science 286, 309-312. doi: 10.1126/science.286.5438.309
-
(1999)
Science
, vol.286
, pp. 309-312
-
-
Joazeiro, C.A.P.1
Wing, S.S.2
Huang, H.3
Leverson, J.D.4
Hunter, T.5
Liu, Y.-C.6
-
116
-
-
65649112466
-
Functional and evolutionary insights into human brain development through global transcriptome analysis
-
Johnson, M. B., Kawasawa, Y. I., Mason, C. E., Krsnik, Z., Coppola, G., Bogdanovic, D.,et al. (2009). Functional and evolutionary insights into human brain development through global transcriptome analysis. Neuron 62, 494-509. doi: 10.1016/j.neuron.2009.03.027
-
(2009)
Neuron
, vol.62
, pp. 494-509
-
-
Johnson, M.B.1
Kawasawa, Y.I.2
Mason, C.E.3
Krsnik, Z.4
Coppola, G.5
Bogdanovic, D.6
-
117
-
-
80052631506
-
Regulation of Notch1 signaling by Delta-like ligand 1 intracellular domain through physical interaction
-
Jung, J., Mo, J. S., Kim, M. Y., Ann, E. J., Yoon, J. H., and Park, H. S. (2011). Regulation of Notch1 signaling by Delta-like ligand 1 intracellular domain through physical interaction. Mol. Cells 32, 161-165. doi: 10.1007/s10059-011-1046-y
-
(2011)
Mol. Cells
, vol.32
, pp. 161-165
-
-
Jung, J.1
Mo, J.S.2
Kim, M.Y.3
Ann, E.J.4
Yoon, J.H.5
Park, H.S.6
-
118
-
-
80052616940
-
Hes1 regulates the number and anterior-posterior patterning of mesencephalic dopaminergic neurons at the mid/hindbrain boundary (isthmus)
-
Kameda, Y., Saitoh, T., and Fujimura, T. (2011). Hes1 regulates the number and anterior-posterior patterning of mesencephalic dopaminergic neurons at the mid/hindbrain boundary (isthmus). Dev. Biol. 358, 91-101. doi: 10.1016/j.ydbio.2011.07.016
-
(2011)
Dev. Biol
, vol.358
, pp. 91-101
-
-
Kameda, Y.1
Saitoh, T.2
Fujimura, T.3
-
119
-
-
84870598651
-
p250GAP is a novel player in the Cdh1-APC/Smurf1 pathway of axon growth regulation.
-
Kannan, M., Lee, S. J., Schwedhelm-Domeyer, N., Nakazawa, T., and Stegmüller, J. (2012). p250GAP is a novel player in the Cdh1-APC/Smurf1 pathway of axon growth regulation. PLoS ONE 7:e50735. doi: 10.1371/journal.pone.0050735
-
(2012)
PLoS ONE
, vol.7
-
-
Kannan, M.1
Lee, S.J.2
Schwedhelm-Domeyer, N.3
Nakazawa, T.4
Stegmüller, J.5
-
120
-
-
84880314687
-
RhoA and Cdc42 are required in pre-migratory progenitors of the medial ganglionic eminence ventricular zone for proper cortical interneuron migration
-
Katayama, K., Imai, F., Campbell, K., Lang, R. A., Zheng, Y., and Yoshida, Y. (2013). RhoA and Cdc42 are required in pre-migratory progenitors of the medial ganglionic eminence ventricular zone for proper cortical interneuron migration. Development. 140, 3139-3145. doi: 10.1242/dev.092585
-
(2013)
Development
, vol.140
, pp. 3139-3145
-
-
Katayama, K.1
Imai, F.2
Campbell, K.3
Lang, R.A.4
Zheng, Y.5
Yoshida, Y.6
-
121
-
-
84900428578
-
Human speech- and reading-related genes display partially overlapping expression patterns in the marmoset brain
-
Kato, M., Okanoya, K., Koike, T., Sasaki, E., Okano, H., Watanabe, S.,et al. (2014). Human speech- and reading-related genes display partially overlapping expression patterns in the marmoset brain. Brain Lang. 133, 26-38. doi: 10.1016/j.bandl.2014.03.007
-
(2014)
Brain Lang
, vol.133
, pp. 26-38
-
-
Kato, M.1
Okanoya, K.2
Koike, T.3
Sasaki, E.4
Okano, H.5
Watanabe, S.6
-
122
-
-
84860505844
-
SFRP1 and SFRP2 dose-dependently regulate midbrain dopamine neuron development in vivo and in embryonic stem cells
-
Kele, J., Andersson, E. R., Villaescusa, J. C., Cajanek, L., Parish, C. L., Bonilla, S.,et al. (2012). SFRP1 and SFRP2 dose-dependently regulate midbrain dopamine neuron development in vivo and in embryonic stem cells. Stem Cells 30, 865-875. doi: 10.1002/stem.1049
-
(2012)
Stem Cells
, vol.30
, pp. 865-875
-
-
Kele, J.1
Andersson, E.R.2
Villaescusa, J.C.3
Cajanek, L.4
Parish, C.L.5
Bonilla, S.6
-
123
-
-
7044269184
-
Hedgehog signaling from the ZLI regulates diencephalic regional identity
-
Kiecker, C., and Lumsden, A. (2004). Hedgehog signaling from the ZLI regulates diencephalic regional identity. Nat. Neurosci. 7, 1242-1249. doi: 10.1038/nn1338
-
(2004)
Nat. Neurosci
, vol.7
, pp. 1242-1249
-
-
Kiecker, C.1
Lumsden, A.2
-
124
-
-
84901059845
-
EGR1-dependent PTEN upregulation by 2-benzoyloxycinnamaldehyde attenuates cell invasion and EMT in colon cancer
-
Kim, J., Kang, H. S., Lee, Y. J., Lee, H. J., Yun, J., Shin, J. H.,et al. (2014). EGR1-dependent PTEN upregulation by 2-benzoyloxycinnamaldehyde attenuates cell invasion and EMT in colon cancer. Cancer Lett. 349, 35-44. doi: 10.1016/j.canlet.2014.03.025
-
(2014)
Cancer Lett
, vol.349
, pp. 35-44
-
-
Kim, J.1
Kang, H.S.2
Lee, Y.J.3
Lee, H.J.4
Yun, J.5
Shin, J.H.6
-
125
-
-
84864603513
-
VCAM1 is essential to maintain the structure of the SVZ niche and acts as an environmental sensor to regulate SVZ lineage progression
-
Kokovay, E., Wang, Y., Kusek, G., Wurster, R., Lederman, P., Lowry, N.,et al. (2012). VCAM1 is essential to maintain the structure of the SVZ niche and acts as an environmental sensor to regulate SVZ lineage progression. Cell Stem Cell. 11, 220-230. doi: 10.1016/j.stem.2012.06.016
-
(2012)
Cell Stem Cell
, vol.11
, pp. 220-230
-
-
Kokovay, E.1
Wang, Y.2
Kusek, G.3
Wurster, R.4
Lederman, P.5
Lowry, N.6
-
126
-
-
1142274208
-
Cdh1-APC controls axonal growth and patterning in the mammalian brain
-
Konishi, Y., Stegmüller, J., Matsuda, T., Bonni, S., and Bonni, A. (2004). Cdh1-APC controls axonal growth and patterning in the mammalian brain. Science 303, 1026-1030. doi: 10.1126/science.1093712
-
(2004)
Science
, vol.303
, pp. 1026-1030
-
-
Konishi, Y.1
Stegmüller, J.2
Matsuda, T.3
Bonni, S.4
Bonni, A.5
-
127
-
-
70449653431
-
Human-specific transcriptional regulation of CNS development genes by FOXP2
-
Konopka, G., Bomar, J. M., Winden, K., Coppola, G., Jonsson, Z. O., Gao, F.,et al. (2009). Human-specific transcriptional regulation of CNS development genes by FOXP2. Nature 462, 213-217. doi: 10.1038/nature08549
-
(2009)
Nature
, vol.462
, pp. 213-217
-
-
Konopka, G.1
Bomar, J.M.2
Winden, K.3
Coppola, G.4
Jonsson, Z.O.5
Gao, F.6
-
128
-
-
84865374280
-
Human-specific transcriptional networks in the brain
-
Konopka, G., Friedrich, T., Davis-Turak, J., Winden, K., Oldham, M. C., Gao, F.,et al. (2012). Human-specific transcriptional networks in the brain. Neuron 75, 601-617. doi: 10.1016/j.neuron.2012.05.034
-
(2012)
Neuron
, vol.75
, pp. 601-617
-
-
Konopka, G.1
Friedrich, T.2
Davis-Turak, J.3
Winden, K.4
Oldham, M.C.5
Gao, F.6
-
129
-
-
0038274073
-
Notch signaling regulates left-right asymmetry determination by inducing Nodal expression
-
Krebs, L. T., Iwai, N., Nonaka, S., Welsh, I. C., Lan, Y., Jiang, R.,et al. (2003). Notch signaling regulates left-right asymmetry determination by inducing Nodal expression. Genes Dev. 17, 1207-1212. doi: 10.1101/gad.1084703
-
(2003)
Genes Dev
, vol.17
, pp. 1207-1212
-
-
Krebs, L.T.1
Iwai, N.2
Nonaka, S.3
Welsh, I.C.4
Lan, Y.5
Jiang, R.6
-
130
-
-
84859268375
-
Neurofascin: a switch between neuronal plasticity and stability
-
Kriebel, M., Wuchter, J., Trinks, S., and Volkmer, H. (2012). Neurofascin: a switch between neuronal plasticity and stability. Int. J. Biochem. Cell. Biol. 44, 694-697. doi: 10.1016/j.biocel.2012.01.012
-
(2012)
Int. J. Biochem. Cell. Biol
, vol.44
, pp. 694-697
-
-
Kriebel, M.1
Wuchter, J.2
Trinks, S.3
Volkmer, H.4
-
131
-
-
84892596990
-
Identification of putative target genes of the transcription factor RUNX2.
-
Kuhlwilm, M., Davierwala, A., and Pääbo, S. (2013). Identification of putative target genes of the transcription factor RUNX2. PLoS ONE 8:e83218. doi: 10.1371/journal.pone.0083218
-
(2013)
PLoS ONE
, vol.8
-
-
Kuhlwilm, M.1
Davierwala, A.2
Pääbo, S.3
-
132
-
-
84857853508
-
Foxp2 mutations impair auditory-motor association learning.
-
Kurt, S, Fisher, S. E., and Ehret, G. (2012). Foxp2 mutations impair auditory-motor association learning. PLoS ONE 7:e33130. doi: 10.1371/journal.pone.0033130
-
(2012)
PLoS ONE
, vol.7
-
-
Kurt, S.1
Fisher, S.E.2
Ehret, G.3
-
133
-
-
0033864070
-
Characterization of ATM mutations in 41 Nordic families with ataxia telangiectasia
-
Laake, K., Jansen, L., Hahnemann, J. M., Brondum-Nielsen, K., Lonnqvist, T., Kaariainen, H.,et al. (2000). Characterization of ATM mutations in 41 Nordic families with ataxia telangiectasia. Hum. Mutat. 16, 232-246. doi: 10.1002/1098-1004(200009)16:3<232::AID-HUMU6>3.0.CO;2-L
-
(2000)
Hum. Mutat
, vol.16
, pp. 232-246
-
-
Laake, K.1
Jansen, L.2
Hahnemann, J.M.3
Brondum-Nielsen, K.4
Lonnqvist, T.5
Kaariainen, H.6
-
134
-
-
0035807360
-
A forkhead-domain gene is mutated in a severe speech and language disorder
-
Lai, C. S., Fisher, S. E., Hurst, J. A., Vargha-Khadem, F., and Monaco, A. P. (2001). A forkhead-domain gene is mutated in a severe speech and language disorder. Nature 413, 519-523. doi: 10.1038/35097076
-
(2001)
Nature
, vol.413
, pp. 519-523
-
-
Lai, C.S.1
Fisher, S.E.2
Hurst, J.A.3
Vargha-Khadem, F.4
Monaco, A.P.5
-
135
-
-
80053532658
-
Ugonin K promotes osteoblastic differentiation and mineralization by activation of p38 MAPK- and ERK-mediated expression of Runx2 and osterix
-
Lee, C. H., Huang, Y. L., Liao, J. F., and Chiou, W. F. (2011). Ugonin K promotes osteoblastic differentiation and mineralization by activation of p38 MAPK- and ERK-mediated expression of Runx2 and osterix. Eur. J. Pharmacol. 668, 383-389. doi: 10.1016/j.ejphar.2011.06.059
-
(2011)
Eur. J. Pharmacol
, vol.668
, pp. 383-389
-
-
Lee, C.H.1
Huang, Y.L.2
Liao, J.F.3
Chiou, W.F.4
-
136
-
-
33846252240
-
Genome-wide atlas of gene expression in the adult mouse brain
-
Lein, E. S., Hawrylycz, M. J., Ao, N., Ayres, M., Bensinger, A., Bernard, A.,et al. (2007). Genome-wide atlas of gene expression in the adult mouse brain. Nature 445, 168-176. doi: 10.1038/nature05453
-
(2007)
Nature
, vol.445
, pp. 168-176
-
-
Lein, E.S.1
Hawrylycz, M.J.2
Ao, N.3
Ayres, M.4
Bensinger, A.5
Bernard, A.6
-
137
-
-
0029809873
-
Requirement of an upstream AP-1 motif for the constitutive and phorbol ester-inducible expression of the urokinase-type plasminogen activator receptor gene
-
Lengyel, E., Wang, H., Stepp, E., Juárez, J., Wang, Y., Doe, W.,et al. (1996). Requirement of an upstream AP-1 motif for the constitutive and phorbol ester-inducible expression of the urokinase-type plasminogen activator receptor gene. J. Biol. Chem. 271, 23176-23184. doi: 10.1074/jbc.271.38.23176
-
(1996)
J. Biol. Chem
, vol.271
, pp. 23176-23184
-
-
Lengyel, E.1
Wang, H.2
Stepp, E.3
Juárez, J.4
Wang, Y.5
Doe, W.6
-
138
-
-
0034863474
-
Telencephalic origin of human thalamic GABAergic neurons
-
Letinic, K., and Rakic, P. (2001). Telencephalic origin of human thalamic GABAergic neurons. Nat. Neurosci. 4, 931-936. doi: 10.1038/nn0901-931
-
(2001)
Nat. Neurosci
, vol.4
, pp. 931-936
-
-
Letinic, K.1
Rakic, P.2
-
139
-
-
0037030677
-
Origin of GABAergic neurons in the human neocortex
-
Letinic, K., Zoncu, R., and Rakic, P. (2002). Origin of GABAergic neurons in the human neocortex. Nature 417, 645-649. doi: 10.1038/nature00779
-
(2002)
Nature
, vol.417
, pp. 645-649
-
-
Letinic, K.1
Zoncu, R.2
Rakic, P.3
-
140
-
-
77953517357
-
Filamin A regulates monocyte migration through Rho small GTPases during osteoclastogenesis
-
Leung, R., Wang, Y., Cuddy, K., Sun, C., Magalhaes, J., Grynpas, M.,et al. (2010). Filamin A regulates monocyte migration through Rho small GTPases during osteoclastogenesis. J. Bone Miner. Res. 25, 1077-1091. doi: 10.1359/jbmr.091114
-
(2010)
J. Bone Miner. Res
, vol.25
, pp. 1077-1091
-
-
Leung, R.1
Wang, Y.2
Cuddy, K.3
Sun, C.4
Magalhaes, J.5
Grynpas, M.6
-
141
-
-
84885410089
-
In and out from the cortex: development of major forebrain connections.
-
Leyva-Díaz, E., and López-Bendito, G. (2013). In and out from the cortex: development of major forebrain connections. Neuroscience 254C, 26-44. doi: 10.1016/j.neuroscience.2013.08.070
-
(2013)
Neuroscience
, vol.254 C
, pp. 26-44
-
-
Leyva-Díaz, E.1
López-Bendito, G.2
-
142
-
-
0034091809
-
Mice deficient in Abl are osteoporotic and have defects in osteoblast maturation
-
Li, B., Boast, S., de los Santos, K., Schieren, I., Quiroz, M., Teitelbaum, S. L.,et al. (2000). Mice deficient in Abl are osteoporotic and have defects in osteoblast maturation. Nat. Genet. 24, 304-308. doi: 10.1038/73542
-
(2000)
Nat. Genet
, vol.24
, pp. 304-308
-
-
Li, B.1
Boast, S.2
De Los Santos, K.3
Schieren, I.4
Quiroz, M.5
Teitelbaum, S.L.6
-
143
-
-
84872076906
-
The neural cell adhesion molecule (NCAM) associates with and signals through p21-activated kinase 1 (Pak1)
-
Li, S., Leshchyns'ka, I., Chernyshova, Y., Schachner, M., and Sytnyk, V. (2013). The neural cell adhesion molecule (NCAM) associates with and signals through p21-activated kinase 1 (Pak1). J. Neurosci. 33, 790-803. doi: 10.1523/JNEUROSCI.1238-12.2013
-
(2013)
J. Neurosci
, vol.33
, pp. 790-803
-
-
Li, S.1
Leshchyns'ka, I.2
Chernyshova, Y.3
Schachner, M.4
Sytnyk, V.5
-
144
-
-
0347986673
-
Transcriptional and DNA binding activity of the Foxp1/2/4 family is modulated by heterotypic and homotypic protein interactions
-
Li, S., Weidenfeld, J., and Morrisey, E. E. (2004). Transcriptional and DNA binding activity of the Foxp1/2/4 family is modulated by heterotypic and homotypic protein interactions. Mol. Cell. Biol. 24, 809-822. doi: 10.1128/MCB.24.2.809-822.2004
-
(2004)
Mol. Cell. Biol
, vol.24
, pp. 809-822
-
-
Li, S.1
Weidenfeld, J.2
Morrisey, E.E.3
-
145
-
-
33846846581
-
The evolution of human speech; its anatomical and neural bases
-
Lieberman, P. (2007). The evolution of human speech; its anatomical and neural bases. Curr. Anthropol. 48, 39-66. doi: 10.1086/509092
-
(2007)
Curr. Anthropol
, vol.48
, pp. 39-66
-
-
Lieberman, P.1
-
146
-
-
80052536392
-
RNA-Seq of human neurons derived from iPS cells reveals candidate long non-coding RNAs involved in neurogenesis and neuropsychiatric disorders.
-
Lin, M., Pedrosa, E., Shah, A., Hrabovsky, A., Maqbool, S., Zheng, D.,et al. (2011). RNA-Seq of human neurons derived from iPS cells reveals candidate long non-coding RNAs involved in neurogenesis and neuropsychiatric disorders. PLoS ONE 6:e23356. doi: 10.1371/journal.pone.0023356.g001
-
(2011)
PLoS ONE
, vol.6
-
-
Lin, M.1
Pedrosa, E.2
Shah, A.3
Hrabovsky, A.4
Maqbool, S.5
Zheng, D.6
-
147
-
-
84860389181
-
A mosaic activating mutation in AKT1 associated with the Proteus syndrome
-
Lindhurst, M. J., Sapp, J. C., Teer, J. K., Johnston, J. J., Finn, E. M., Peters, K.,et al. (2011). A mosaic activating mutation in AKT1 associated with the Proteus syndrome. New. Eng. J. Med. 365, 611-619. doi: 10.1056/NEJMoa1104017
-
(2011)
New. Eng. J. Med
, vol.365
, pp. 611-619
-
-
Lindhurst, M.J.1
Sapp, J.C.2
Teer, J.K.3
Johnston, J.J.4
Finn, E.M.5
Peters, K.6
-
148
-
-
84859541449
-
Extension of cortical synaptic development distinguishes humans from chimpanzees and macaques
-
Liu, X., Somel, M., Tang, L., Yan, Z., Jiang, X., Guo, S.,et al. (2012). Extension of cortical synaptic development distinguishes humans from chimpanzees and macaques. Genome Res. 22, 611-622. doi: 10.1101/gr.127324.111
-
(2012)
Genome Res
, vol.22
, pp. 611-622
-
-
Liu, X.1
Somel, M.2
Tang, L.3
Yan, Z.4
Jiang, X.5
Guo, S.6
-
149
-
-
47749150635
-
Phosphorylation of protein kinase Cdelta on distinct tyrosine residues induces sustained activation of Erk1/2 via down-regulation of MKP-1: role in the apoptotic effect of etoposide
-
Lomonaco, S. L., Kahana, S., Blass, M., Brody, Y., Okhrimenko, H., Xiang, C.,et al. (2008). Phosphorylation of protein kinase Cdelta on distinct tyrosine residues induces sustained activation of Erk1/2 via down-regulation of MKP-1: role in the apoptotic effect of etoposide. J. Biol. Chem. 283, 17731-17739. doi: 10.1074/jbc. M801727200
-
(2008)
J. Biol. Chem
, vol.283
, pp. 17731-17739
-
-
Lomonaco, S.L.1
Kahana, S.2
Blass, M.3
Brody, Y.4
Okhrimenko, H.5
Xiang, C.6
-
150
-
-
33947542776
-
Dlx-dependent and -independent regulation of olfactory bulb interneuron differentiation
-
Long, J. E., Garel, S., álvarez-Dolado, M., Yoshikawa, K., Osumi, N., álvarez-Buylla, A.,et al. (2007). Dlx-dependent and -independent regulation of olfactory bulb interneuron differentiation. J. Neurosci. 27, 3230-3243. doi: 10.1523/JNEUROSCI.5265-06.2007
-
(2007)
J. Neurosci
, vol.27
, pp. 3230-3243
-
-
Long, J.E.1
Garel, S.2
álvarez-Dolado, M.3
Yoshikawa, K.4
Osumi, N.5
álvarez-Buylla, A.6
-
151
-
-
84883768766
-
Genetically engineered bone marrow mesenchymal stem cells improve functional outcome in a rat model of epilepsy
-
Long, Q., Qiu, B., Wang, K., Yang, J., Jia, C., Xin, W.,et al. (2013). Genetically engineered bone marrow mesenchymal stem cells improve functional outcome in a rat model of epilepsy. Brain. Res. 1532, 1-13. doi: 10.1016/j.brainres.2013.07.020
-
(2013)
Brain. Res
, vol.1532
, pp. 1-13
-
-
Long, Q.1
Qiu, B.2
Wang, K.3
Yang, J.4
Jia, C.5
Xin, W.6
-
152
-
-
79952012639
-
Loss of Cited2 causes congenital heart disease by perturbing left-right patterning of the body axis
-
Lopes Floro, K., Artap, S. T., Preis, J. I., Fatkin, D., Chapman, G., Furtado, M. B.,et al. (2011). Loss of Cited2 causes congenital heart disease by perturbing left-right patterning of the body axis. Hum. Mol. Genet. 20, 1097-1110. doi: 10.1093/hmg/ddq554
-
(2011)
Hum. Mol. Genet
, vol.20
, pp. 1097-1110
-
-
Lopes Floro, K.1
Artap, S.T.2
Preis, J.I.3
Fatkin, D.4
Chapman, G.5
Furtado, M.B.6
-
153
-
-
34047138896
-
Robo1 and Robo2 cooperate to control the guidance of major axonal tracts in the mammalian forebrain
-
López-Bendito, G., Flames, N., Ma, L., Fouquet, C., Di Meglio, T., Chedotal, A.,et al. (2007). Robo1 and Robo2 cooperate to control the guidance of major axonal tracts in the mammalian forebrain. J. Neurosci. 27, 3395-3407. doi: 10.1523/JNEUROSCI.4605-06.2007
-
(2007)
J. Neurosci
, vol.27
, pp. 3395-3407
-
-
López-Bendito, G.1
Flames, N.2
Ma, L.3
Fouquet, C.4
Di Meglio, T.5
Chedotal, A.6
-
154
-
-
0029913091
-
Conserved left-right asymmetry of nodal expression and alterations in murine situs inversus
-
Lowe, L. A., Supp, D. M., Sampath, K., Yokoyama, T., Wright, C. V., Potter, S. S.,et al. (1996). Conserved left-right asymmetry of nodal expression and alterations in murine situs inversus. Nature 381, 158-161. doi: 10.1038/381158a0
-
(1996)
Nature
, vol.381
, pp. 158-161
-
-
Lowe, L.A.1
Supp, D.M.2
Sampath, K.3
Yokoyama, T.4
Wright, C.V.5
Potter, S.S.6
-
155
-
-
14244263713
-
Gene expression profiling of leiomyoma and myometrial smooth muscle cells in response to transforming growth factor-beta
-
Luo, X., Ding, L., Xu, J., and Chegini, N. (2005). Gene expression profiling of leiomyoma and myometrial smooth muscle cells in response to transforming growth factor-beta. Endocrinology 146, 1097-1118. doi: 10.1210/en.2004-1377
-
(2005)
Endocrinology
, vol.146
, pp. 1097-1118
-
-
Luo, X.1
Ding, L.2
Xu, J.3
Chegini, N.4
-
156
-
-
21044445447
-
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits
-
MacDermot, K. D., Bonora, E., Sykes, N., Coupe, A. M., Lai, C. S., Vernes, S. C.,et al. (2005). Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. Am. J. Hum. Genet. 76, 1074-1080. doi: 10.1086/430841
-
(2005)
Am. J. Hum. Genet
, vol.76
, pp. 1074-1080
-
-
MacDermot, K.D.1
Bonora, E.2
Sykes, N.3
Coupe, A.M.4
Lai, C.S.5
Vernes, S.C.6
-
157
-
-
15844384360
-
Functional and physical interactions between mammalian achaete-scute homolog 1 and myocyte enhancer factor 2A
-
Mao, Z., and Nadal-Ginard, B. (1996). Functional and physical interactions between mammalian achaete-scute homolog 1 and myocyte enhancer factor 2A. J. Biol. Chem. 271, 14371-14375. doi: 10.1074/jbc.271.24.14371
-
(1996)
J. Biol. Chem
, vol.271
, pp. 14371-14375
-
-
Mao, Z.1
Nadal-Ginard, B.2
-
158
-
-
84859047412
-
The lhx2 transcription factor controls thalamocortical axonal guidance by specific regulation of robo1 and robo2 receptors
-
Marcos-Mondéjar, P., Peregrín, S., Li, J. Y., Carlsson, L., Tole, S., and López-Bendito, G. (2012). The lhx2 transcription factor controls thalamocortical axonal guidance by specific regulation of robo1 and robo2 receptors. J. Neurosci. 32, 4372-4385. doi: 10.1523/JNEUROSCI.5851-11.2012
-
(2012)
J. Neurosci
, vol.32
, pp. 4372-4385
-
-
Marcos-Mondéjar, P.1
Peregrín, S.2
Li, J.Y.3
Carlsson, L.4
Tole, S.5
López-Bendito, G.6
-
159
-
-
84891941306
-
Altered miRNA expression is associated with neuronal fate in G93A-SOD1 ependymal stem progenitor cells
-
Marcuzzo, S., Kapetis, D., Mantegazza, R., Baggi, F., Bonanno, S., Barzago, C.,et al. (2014). Altered miRNA expression is associated with neuronal fate in G93A-SOD1 ependymal stem progenitor cells. Exp. Neurol. 253, 91-101. doi: 10.1016/j.expneurol.2013.12.007
-
(2014)
Exp. Neurol
, vol.253
, pp. 91-101
-
-
Marcuzzo, S.1
Kapetis, D.2
Mantegazza, R.3
Baggi, F.4
Bonanno, S.5
Barzago, C.6
-
160
-
-
84875614116
-
A recent evolutionary change affects a regulatory element in the human FOXP2 gene
-
Maricic, T., Günther, V., Georgiev, O., Gehre, S., Curlin, M., Schreiweis, C.,et al. (2013). A recent evolutionary change affects a regulatory element in the human FOXP2 gene. Mol. Biol. Evol. 30, 844-852. doi: 10.1093/molbev/mss271
-
(2013)
Mol. Biol. Evol
, vol.30
, pp. 844-852
-
-
Maricic, T.1
Günther, V.2
Georgiev, O.3
Gehre, S.4
Curlin, M.5
Schreiweis, C.6
-
161
-
-
0037039172
-
Spatiotemporal expression patterns of slit and robo genes in the rat brain
-
Marillat, V., Cases, O., Nguyenf Ba-Charvet, K. T., TessierLavigne, M., Sotelo, C., and Chédotal, A. (2002). Spatiotemporal expression patterns of slit and robo genes in the rat brain. J. Comp. Neurol. 442, 130-155. doi: 10.1002/cne.10068
-
(2002)
J. Comp. Neurol
, vol.442
, pp. 130-155
-
-
Marillat, V.1
Cases, O.2
Nguyenf Ba-Charvet, K.T.3
TessierLavigne, M.4
Sotelo, C.5
Chédotal, A.6
-
162
-
-
77955583599
-
Heterozygous germline mutations in the CBL tumor-suppressor gene cause a Noonan syndrome-like phenotype
-
Martinelli, S., De Luca, A., Stellacci, E., Rossi, C., Checquolo, S., Lepri, F.,et al. (2010). Heterozygous germline mutations in the CBL tumor-suppressor gene cause a Noonan syndrome-like phenotype. Am. J. Hum. Genet. 87, 250-257. doi: 10.1016/j.ajhg.2010.06.015
-
(2010)
Am. J. Hum. Genet
, vol.87
, pp. 250-257
-
-
Martinelli, S.1
De Luca, A.2
Stellacci, E.3
Rossi, C.4
Checquolo, S.5
Lepri, F.6
-
163
-
-
84899569504
-
KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia
-
Mascheretti, S., Riva, V., Giorda, R., Beri, S., Lanzoni, L. F., Cellino, M. R.,et al. (2014). KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia. J. Hum. Genet. 59, 189-197. doi: 10.1038/jhg.2013.141
-
(2014)
J. Hum. Genet
, vol.59
, pp. 189-197
-
-
Mascheretti, S.1
Riva, V.2
Giorda, R.3
Beri, S.4
Lanzoni, L.F.5
Cellino, M.R.6
-
164
-
-
84864660417
-
ABL1 joins the cadre of spindle orientation machinery
-
Matsumura, S., and Toyoshima, F. (2012). ABL1 joins the cadre of spindle orientation machinery. Cell. Struct. Funct. 37, 81-87. doi: 10.1247/csf.12011
-
(2012)
Cell. Struct. Funct
, vol.37
, pp. 81-87
-
-
Matsumura, S.1
Toyoshima, F.2
-
165
-
-
79251632187
-
Suppression of osteosarcoma cell invasion by chemotherapy is mediated by urokinase plasminogen activator activity via up-regulation of EGR1.
-
Matsunoshita, Y., Ijiri, K., Ishidou, Y., Nagano, S., Yamamoto, T., Nagao, H.,et al. (2011). Suppression of osteosarcoma cell invasion by chemotherapy is mediated by urokinase plasminogen activator activity via up-regulation of EGR1. PLoS ONE 6:e16234. doi: 10.1371/journal.pone.0016234
-
(2011)
PLoS ONE
, vol.6
-
-
Matsunoshita, Y.1
Ijiri, K.2
Ishidou, Y.3
Nagano, S.4
Yamamoto, T.5
Nagao, H.6
-
166
-
-
18444381728
-
Knockout of ERK1 MAP kinase enhances synaptic plasticity in the striatum and facilitates striatal-mediated learning and memory
-
Mazzucchelli, C., Vantaggiato, C., Ciamei, A., Fasano, S., Pakhotin, P., Krezel, W.,et al. (2002). Knockout of ERK1 MAP kinase enhances synaptic plasticity in the striatum and facilitates striatal-mediated learning and memory. Neuron 34, 807-820. doi: 10.1016/S0896-6273(02)00716-X
-
(2002)
Neuron
, vol.34
, pp. 807-820
-
-
Mazzucchelli, C.1
Vantaggiato, C.2
Ciamei, A.3
Fasano, S.4
Pakhotin, P.5
Krezel, W.6
-
167
-
-
0037154872
-
Transcriptional regulation of cortical neuron migration by POU domain factors
-
McEvilly, R. J., de Díaz, M. O., Schonemann, M. D., Hooshmand, F., and Rosenfeld, M. G. (2002). Transcriptional regulation of cortical neuron migration by POU domain factors. Science 295, 1528-1532. doi: 10.1126/science.1067132
-
(2002)
Science
, vol.295
, pp. 1528-1532
-
-
McEvilly, R.J.1
de Díaz, M.O.2
Schonemann, M.D.3
Hooshmand, F.4
Rosenfeld, M.G.5
-
168
-
-
79952386187
-
Human-specific loss of regulatory DNA and the evolution of human-specific traits
-
McLean, C. Y., Reno, P. L., Pollen, A. A., Bassan, A. I., Capellini, T. D., Guenther, C.,et al. (2011). Human-specific loss of regulatory DNA and the evolution of human-specific traits. Nature 471, 216-219. doi: 10.1038/nature09774
-
(2011)
Nature
, vol.471
, pp. 216-219
-
-
McLean, C.Y.1
Reno, P.L.2
Pollen, A.A.3
Bassan, A.I.4
Capellini, T.D.5
Guenther, C.6
-
169
-
-
84899843251
-
Evolutionary and developmental contributions for understanding the organization of the Basal Ganglia
-
Medina, L., Abellán, A., Vicario, A., and Desfilis, E. (2014). Evolutionary and developmental contributions for understanding the organization of the Basal Ganglia. Brain Behav. Evol. 83, 112-125. doi: 10.1159/000357832
-
(2014)
Brain Behav. Evol
, vol.83
, pp. 112-125
-
-
Medina, L.1
Abellán, A.2
Vicario, A.3
Desfilis, E.4
-
170
-
-
84867331947
-
A high-coverage genome sequence from an archaic Denisovan individual
-
Meyer, M., Kircher, M., Gansauge, M. T., Li, H., Racimo, F., Mallick, S.,et al. (2012). A high-coverage genome sequence from an archaic Denisovan individual. Science 338, 222-226. doi: 10.1126/science.1224344
-
(2012)
Science
, vol.338
, pp. 222-226
-
-
Meyer, M.1
Kircher, M.2
Gansauge, M.T.3
Li, H.4
Racimo, F.5
Mallick, S.6
-
171
-
-
0035977716
-
Radical fringe negatively modulates Notch signaling in postmitotic neurons of the rat brain
-
Mikami, T., Ohnaka, Y., Nakamura, A., Kurosaka, A., and Itoh, N. (2001). Radical fringe negatively modulates Notch signaling in postmitotic neurons of the rat brain. Brain. Res. Mol. Brain. Res. 86, 138-144. doi: 10.1016/S0169-328X(00)00278-3
-
(2001)
Brain. Res. Mol. Brain. Res
, vol.86
, pp. 138-144
-
-
Mikami, T.1
Ohnaka, Y.2
Nakamura, A.3
Kurosaka, A.4
Itoh, N.5
-
172
-
-
84921603495
-
Rules through recursion: how interactions between the frontal cortex and basal ganglia may build abstract, complex, rules from concrete, simple, ones
-
eds S. Bunge and J. Wallis (Oxford: Oxford University Press)
-
Miller, E. K., and Buschman, T. J. (2007). "Rules through recursion: how interactions between the frontal cortex and basal ganglia may build abstract, complex, rules from concrete, simple, ones," in The Neuroscience of Rule-Guided Behavior, eds S. Bunge and J. Wallis (Oxford: Oxford University Press), 419-440.
-
(2007)
In The Neuroscience of Rule-Guided Behavior
, pp. 419-440
-
-
Miller, E.K.1
Buschman, T.J.2
-
173
-
-
84900303453
-
Transcriptional landscape of the prenatal human brain
-
Miller, J. A., Ding, S. L., Sunkin, S. M., Smith, K. A., Ng, L., Szafer, A.,et al. (2014). Transcriptional landscape of the prenatal human brain. Nature 508, 199-206. doi: 10.1038/nature13185
-
(2014)
Nature
, vol.508
, pp. 199-206
-
-
Miller, J.A.1
Ding, S.L.2
Sunkin, S.M.3
Smith, K.A.4
Ng, L.5
Szafer, A.6
-
174
-
-
0030803279
-
Interaction and functional collaboration of p300 and C/EBPß
-
Mink, S., Haenig, B., and Klempnauer, K. H. (1997). Interaction and functional collaboration of p300 and C/EBPß. Mol. Cell. Biol. 17, 6609-6617.
-
(1997)
Mol. Cell. Biol.
, vol.17
, pp. 6609-6617
-
-
Mink, S.1
Haenig, B.2
Klempnauer, K.H.3
-
175
-
-
77956236967
-
Purinergic receptor-mediated rapid depletion of nuclear phosphorylated Akt depends on pleckstrin homology domain leucine-rich repeat phosphatase, calcineurin, protein phosphatase 2A, and PTEN phosphatases
-
Mistafa, O., Ghalali, A., Kadekar, S., Högberg, J., and Stenius, U. (2010). Purinergic receptor-mediated rapid depletion of nuclear phosphorylated Akt depends on pleckstrin homology domain leucine-rich repeat phosphatase, calcineurin, protein phosphatase 2A, and PTEN phosphatases. J. Biol. Chem. 285, 27900-27910. doi: 10.1074/jbc. M110.117093
-
(2010)
J. Biol. Chem
, vol.285
, pp. 27900-27910
-
-
Mistafa, O.1
Ghalali, A.2
Kadekar, S.3
Högberg, J.4
Stenius, U.5
-
177
-
-
1942504197
-
DISC1 localizes to the centrosome by binding to kendrin
-
Miyoshi, K., Asanuma, M., Miyazaki, I., Díaz-Corrales, F. J., Katayama, T., Tohyama, M.,et al. (2004). DISC1 localizes to the centrosome by binding to kendrin. Biochem. Biophys. Res. Commun. 317, 1195-1199. doi: 10.1016/j.bbrc.2004.03.163
-
(2004)
Biochem. Biophys. Res. Commun
, vol.317
, pp. 1195-1199
-
-
Miyoshi, K.1
Asanuma, M.2
Miyazaki, I.3
Díaz-Corrales, F.J.4
Katayama, T.5
Tohyama, M.6
-
178
-
-
0035811573
-
Regulation of Cbl phosphorylation by the Abl tyrosine kinase and the Nck SH2/SH3 adaptor
-
Miyoshi-Akiyama, T., Alemán, L. M., Smith, J. M., Adler, C. E., and Mayer, B. J. (2001). Regulation of Cbl phosphorylation by the Abl tyrosine kinase and the Nck SH2/SH3 adaptor. Oncogene 20, 4058-4069. doi: 10.1038/sj.onc.1204528
-
(2001)
Oncogene
, vol.20
, pp. 4058-4069
-
-
Miyoshi-Akiyama, T.1
Alemán, L.M.2
Smith, J.M.3
Adler, C.E.4
Mayer, B.J.5
-
179
-
-
84896374339
-
Genome-wide association study reveals two new risk loci for bipolar disorder
-
Mühleisen, T. W., Leber, M., Schulze, T. G., Strohmaier, J., Degenhardt, F., Treutlein, J.,et al. (2014). Genome-wide association study reveals two new risk loci for bipolar disorder. Nat. Commun. 5:3339. doi: 10.1038/ncomms4339
-
(2014)
Nat. Commun
, vol.5
, pp. 3339
-
-
Mühleisen, T.W.1
Leber, M.2
Schulze, T.G.3
Strohmaier, J.4
Degenhardt, F.5
Treutlein, J.6
-
180
-
-
84869128239
-
Focal adhesion kinase modulates Cdc42 activity downstream of positive and negative axon guidance cues
-
Myers, J. P., Robles, E., Ducharme-Smith, A., and Gómez, T. M. (2012). Focal adhesion kinase modulates Cdc42 activity downstream of positive and negative axon guidance cues. J. Cell. Sci. 125, 2918-2929. doi: 10.1242/jcs.100107
-
(2012)
J. Cell. Sci
, vol.125
, pp. 2918-2929
-
-
Myers, J.P.1
Robles, E.2
Ducharme-Smith, A.3
Gómez, T.M.4
-
181
-
-
84902996473
-
Mammalian-specific sequences in Pou3f2 contribute to maternal behavior
-
Nasu, M., Yada, S., Igarashi, A., Sutoo, D., Akiyama, K., Ito, M.,et al. (2014). Mammalian-specific sequences in Pou3f2 contribute to maternal behavior. Genome Biol. Evol. 6, 1145-1156. doi: 10.1093/gbe/evu072
-
(2014)
Genome Biol. Evol
, vol.6
, pp. 1145-1156
-
-
Nasu, M.1
Yada, S.2
Igarashi, A.3
Sutoo, D.4
Akiyama, K.5
Ito, M.6
-
182
-
-
52249101375
-
Targeted disruption of the Pak5 and Pak6 genes in mice leads to deficits in learning and locomotion
-
Nekrasova, T., Jobes, M. L., Ting, J. H., Wagner, G. C., and Minden, A. (2008). Targeted disruption of the Pak5 and Pak6 genes in mice leads to deficits in learning and locomotion. Dev. Biol. 322, 95-108. doi: 10.1016/j.ydbio.2008.07.006
-
(2008)
Dev. Biol
, vol.322
, pp. 95-108
-
-
Nekrasova, T.1
Jobes, M.L.2
Ting, J.H.3
Wagner, G.C.4
Minden, A.5
-
183
-
-
84880213877
-
Microfluidic affinity and ChIP-seq analyses converge on a conserved FOXP2-binding motif in chimp and human, which enables the detection of evolutionarily novel targets
-
Nelson, C. S., Fuller, C. K., Fordyce, P. M., Greninger, A. L., Li, H., and DeRisi, J. L. (2013). Microfluidic affinity and ChIP-seq analyses converge on a conserved FOXP2-binding motif in chimp and human, which enables the detection of evolutionarily novel targets. Nucleic Acids Res. 41, 5991-6004. doi: 10.1093/nar/gkt259
-
(2013)
Nucleic Acids Res
, vol.41
, pp. 5991-6004
-
-
Nelson, C.S.1
Fuller, C.K.2
Fordyce, P.M.3
Greninger, A.L.4
Li, H.5
DeRisi, J.L.6
-
184
-
-
44949169517
-
Relationship between Delta-like and proneural bHLH genes during chick retinal development
-
Nelson, B. R., and Reh, T. A. (2008). Relationship between Delta-like and proneural bHLH genes during chick retinal development. Dev. Dyn. 237, 1565-1580. doi: 10.1002/dvdy.21550
-
(2008)
Dev. Dyn
, vol.237
, pp. 1565-1580
-
-
Nelson, B.R.1
Reh, T.A.2
-
185
-
-
68249126179
-
CMIP and ATP2C2 modulate phonological short-term memory in language impairment
-
Newbury, D. F., Winchester, L., Addis, L., Paracchini, S., Buckingham, L. L., Clark, A.,et al. (2009). CMIP and ATP2C2 modulate phonological short-term memory in language impairment. Am. J. Hum. Genet. 85, 264-272. doi: 10.1016/j.ajhg.2009.07.004
-
(2009)
Am. J. Hum. Genet
, vol.85
, pp. 264-272
-
-
Newbury, D.F.1
Winchester, L.2
Addis, L.3
Paracchini, S.4
Buckingham, L.L.5
Clark, A.6
-
186
-
-
23944434184
-
Human p53 tumor suppressor gene (TP53) and schizophrenia: case-control and family studies
-
Ni, X., Trakalo, J., Valente, J., Azevedo, M. H., Pato, M. T., Pato, C. N.,et al. (2005). Human p53 tumor suppressor gene (TP53) and schizophrenia: case-control and family studies. Neurosci. Lett. 388, 173-178. doi: 10.1016/j.neulet.2005.06.050
-
(2005)
Neurosci. Lett
, vol.388
, pp. 173-178
-
-
Ni, X.1
Trakalo, J.2
Valente, J.3
Azevedo, M.H.4
Pato, M.T.5
Pato, C.N.6
-
187
-
-
10444279104
-
Direct interaction between Smad3, APC10, CDH1 and HEF1 in proteasomal degradation of HEF1
-
Nourry, C., Maksumova, L., Pang, M., Liu, X., and Wang, T. (2004). Direct interaction between Smad3, APC10, CDH1 and HEF1 in proteasomal degradation of HEF1. BMC Cell Biol. 5:20. doi: 10.1186/1471-2121-5-20
-
(2004)
BMC Cell Biol
, vol.5
, pp. 20
-
-
Nourry, C.1
Maksumova, L.2
Pang, M.3
Liu, X.4
Wang, T.5
-
188
-
-
84860014572
-
The p250GAP gene is associated with risk for schizophrenia and schizotypal personality traits.
-
Ohi, K., Hashimoto, R., Nakazawa, T., Okada, T., Yasuda, Y., Yamamori, H.,et al. (2012). The p250GAP gene is associated with risk for schizophrenia and schizotypal personality traits. PLoS ONE 7:e35696. doi: 10.1371/journal.pone.0035696
-
(2012)
PLoS ONE
, vol.7
-
-
Ohi, K.1
Hashimoto, R.2
Nakazawa, T.3
Okada, T.4
Yasuda, Y.5
Yamamori, H.6
-
189
-
-
84897130215
-
The human condition-a molecular approach
-
Pääbo, S. (2014). The human condition-a molecular approach. Cell 157, 216-226. doi: 10.1016/j.cell.2013.12.036
-
(2014)
Cell
, vol.157
, pp. 216-226
-
-
Pääbo, S.1
-
190
-
-
43549123531
-
The role of the PTEN/AKT Pathway in NOTCH1-induced leukemia
-
Palomero, T., Domínguez, M., and Ferrando, A. A. (2008). The role of the PTEN/AKT Pathway in NOTCH1-induced leukemia. Cell Cycle 7, 965-970. doi: 10.4161/cc.7.8.5753
-
(2008)
Cell Cycle
, vol.7
, pp. 965-970
-
-
Palomero, T.1
Domínguez, M.2
Ferrando, A.A.3
-
191
-
-
84872463245
-
The TP53 fertility network
-
Paskulin, D. D., Paixão-Côrtes, V. R., Hainaut, P., Bortolini, M. C., and Ashton-Prolla, P. (2012). The TP53 fertility network. Genet. Mol. Biol. 35, 939-946. doi: 10.1590/S1415-47572012000600008
-
(2012)
Genet. Mol. Biol
, vol.35
, pp. 939-946
-
-
Paskulin, D.D.1
Paixão-Côrtes, V.R.2
Hainaut, P.3
Bortolini, M.C.4
Ashton-Prolla, P.5
-
192
-
-
78649665537
-
Identification of a microdeletion at the 7q33-q35 disrupting the CNTNAP2 gene in a Brazilian stuttering case.
-
Petrin, A. L., Giacheti, C. M., Maximino, L. P., Abramides, D. V., Zanchetta, S., Rossi, N. F.,et al. (2010). Identification of a microdeletion at the 7q33-q35 disrupting the CNTNAP2 gene in a Brazilian stuttering case. Am. J. Med. Genet. A 152A, 3164-3172. doi: 10.1002/ajmg.a.33749
-
(2010)
Am. J. Med. Genet. A
, vol.152 A
, pp. 3164-3172
-
-
Petrin, A.L.1
Giacheti, C.M.2
Maximino, L.P.3
Abramides, D.V.4
Zanchetta, S.5
Rossi, N.F.6
-
193
-
-
84923325231
-
-
Ph. D. thesis, Duke University, Durham.
-
Pfenning, A. R. (2012). A Computational Synthesis of Genes, Behavior, and Evolution Provides Insights into the Molecular Basis of Vocal Learning. Ph. D. thesis, Duke University, Durham.
-
(2012)
A Computational Synthesis of Genes, Behavior, and Evolution Provides Insights into the Molecular Basis of Vocal Learning.
-
-
Pfenning, A.R.1
-
194
-
-
79953065216
-
A theoretical molecular network for dyslexia: integrating available genetic findings
-
Poelmans, G., Buitelaar, J. K., Pauls, D. L., and Franke, B. (2011). A theoretical molecular network for dyslexia: integrating available genetic findings. Mol. Psychiatry 16, 365-382. doi: 10.1038/mp.2010.105
-
(2011)
Mol. Psychiatry
, vol.16
, pp. 365-382
-
-
Poelmans, G.1
Buitelaar, J.K.2
Pauls, D.L.3
Franke, B.4
-
195
-
-
57749203394
-
A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype
-
Potkin, S. G., Turner, J. A., Guffanti, G., Lakatos, A., Fallon, J. H., Nguyen, D. D.,et al. (2009). A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. Schizophr. Bull. 35, 96-108. doi: 10.1093/schbul/sbn155
-
(2009)
Schizophr. Bull
, vol.35
, pp. 96-108
-
-
Potkin, S.G.1
Turner, J.A.2
Guffanti, G.3
Lakatos, A.4
Fallon, J.H.5
Nguyen, D.D.6
-
196
-
-
0037081617
-
NCAM regulates cell motility
-
Prag, S., Lepekhin, E. A., Kolkova, K., Hartmann-Petersen, R., Kawa, A., Walmod, P. S.,et al. (2002). NCAM regulates cell motility. J. Cell Sci. 115, 283-292.
-
(2002)
J. Cell Sci.
, vol.115
, pp. 283-292
-
-
Prag, S.1
Lepekhin, E.A.2
Kolkova, K.3
Hartmann-Petersen, R.4
Kawa, A.5
Walmod, P.S.6
-
197
-
-
33845977042
-
Generation of conditional Cited2 null alleles
-
Preis, J. I., Wise, N., Solloway, M. J., Harvey, R. P., Sparrow, D. B., and Dunwoodie, S. L. (2006). Generation of conditional Cited2 null alleles. Genesis 44, 579-583. doi: 10.1002/dvg.20251
-
(2006)
Genesis
, vol.44
, pp. 579-583
-
-
Preis, J.I.1
Wise, N.2
Solloway, M.J.3
Harvey, R.P.4
Sparrow, D.B.5
Dunwoodie, S.L.6
-
198
-
-
84892365780
-
The complete genome sequence of a Neanderthal from the Altai Mountains
-
Prüfer, K., Racimo, F., Patterson, N., Jay, F., Sankararaman, S., Sawyer, S.,et al. (2014). The complete genome sequence of a Neanderthal from the Altai Mountains. Nature 505, 43-49. doi: 10.1038/nature12886
-
(2014)
Nature
, vol.505
, pp. 43-49
-
-
Prüfer, K.1
Racimo, F.2
Patterson, N.3
Jay, F.4
Sankararaman, S.5
Sawyer, S.6
-
199
-
-
84855374973
-
Dysregulation of Rho GTPases in the aPix/Arhgef6 mouse model of X-linked intellectual disability is paralleled by impaired structural and synaptic plasticity and cognitive deficits
-
Ramakers, G. J., Wolfer, D., Rosenberger, G., Kuchenbecker, K., Kreienkamp, H. J., Prange-Kiel, J.,et al. (2012). Dysregulation of Rho GTPases in the aPix/Arhgef6 mouse model of X-linked intellectual disability is paralleled by impaired structural and synaptic plasticity and cognitive deficits. Hum. Mol. Genet. 21, 268-286. doi: 10.1093/hmg/ddr457
-
(2012)
Hum. Mol. Genet
, vol.21
, pp. 268-286
-
-
Ramakers, G.J.1
Wolfer, D.2
Rosenberger, G.3
Kuchenbecker, K.4
Kreienkamp, H.J.5
Prange-Kiel, J.6
-
200
-
-
38949087294
-
Mutations in the pericentrin (PCNT) gene cause primordial dwarfism
-
Rauch, A., Thiel, C. T., Schindler, D., Wick, U., Crow, Y. J., Ekici, A. B.,et al. (2008). Mutations in the pericentrin (PCNT) gene cause primordial dwarfism. Science 319, 816-819. doi: 10.1126/science.1151174
-
(2008)
Science
, vol.319
, pp. 816-819
-
-
Rauch, A.1
Thiel, C.T.2
Schindler, D.3
Wick, U.4
Crow, Y.J.5
Ekici, A.B.6
-
201
-
-
84872852868
-
The transcription factor Runx2 is under circadian control in the suprachiasmatic nucleus and functions in the control of rhythmic behavior.
-
Reale, M. E., Webb, I. C., Wang, X., Baltazar, R. M., Coolen, L. M., and Lehman, M. N. (2013). The transcription factor Runx2 is under circadian control in the suprachiasmatic nucleus and functions in the control of rhythmic behavior. PLoS ONE 8:e54317. doi: 10.1371/journal.pone.0054317
-
(2013)
PLoS ONE
, vol.8
-
-
Reale, M.E.1
Webb, I.C.2
Wang, X.3
Baltazar, R.M.4
Coolen, L.M.5
Lehman, M.N.6
-
202
-
-
0031737286
-
Lhx2, a vertebrate homologue of apterous, regulates vertebrate limb outgrowth
-
Rodríguez-Esteban, C., Schwabe, J. W., Peña, J. D., Rincón-Limas, D. E., Magallón, J., Botas, J.,et al. (1998). Lhx2, a vertebrate homologue of apterous, regulates vertebrate limb outgrowth. Development 125, 3925-3934.
-
(1998)
Development
, vol.125
, pp. 3925-3934
-
-
Rodríguez-Esteban, C.1
Schwabe, J.W.2
Peña, J.D.3
Rincón-Limas, D.E.4
Magallón, J.5
Botas, J.6
-
203
-
-
33645115357
-
SRPX2 mutations in disorders of language cortex and cognition
-
Roll, P., Rudolf, G., Pereira, S., Royer, B., Scheffer, I. E., Massacrier, A.,et al. (2006). SRPX2 mutations in disorders of language cortex and cognition. Hum. Mol. Genet. 15, 1195-1207. doi: 10.1093/hmg/ddl035
-
(2006)
Hum. Mol. Genet
, vol.15
, pp. 1195-1207
-
-
Roll, P.1
Rudolf, G.2
Pereira, S.3
Royer, B.4
Scheffer, I.E.5
Massacrier, A.6
-
204
-
-
78649477258
-
Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex
-
Roll, P., Vernes, S. C., Bruneau, N., Cillario, J., Ponsole-Lenfant, M., Massacrier, A.,et al. (2010). Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex. Hum. Mol. Genet. 19, 4848-4860. doi: 10.1093/hmg/ddq415
-
(2010)
Hum. Mol. Genet
, vol.19
, pp. 4848-4860
-
-
Roll, P.1
Vernes, S.C.2
Bruneau, N.3
Cillario, J.4
Ponsole-Lenfant, M.5
Massacrier, A.6
-
205
-
-
0034011003
-
The neural cell adhesion molecule in synaptic plasticity and ageing
-
Rønn, L. C., Berezin, V., and Bock, E. (2000). The neural cell adhesion molecule in synaptic plasticity and ageing. Int. J. Dev. Neurosci. 18, 193-199. doi: 10.1016/S0736-5748(99)00088-X
-
(2000)
Int. J. Dev. Neurosci
, vol.18
, pp. 193-199
-
-
Rønn, L.C.1
Berezin, V.2
Bock, E.3
-
206
-
-
56049086389
-
Epileptic and developmental disorders of the speech cortex: ligand/receptor interaction of wild-type and mutant SRPX2 with the plasminogen activator receptor uPAR
-
Royer-Zemmour, B., Ponsole-Lenfant, M., Gara, H., Roll, P., Lévêque, C., Massacrier, A.,et al. (2008). Epileptic and developmental disorders of the speech cortex: ligand/receptor interaction of wild-type and mutant SRPX2 with the plasminogen activator receptor uPAR. Hum. Mol. Genet. 17, 3617-3630. doi: 10.1093/hmg/ddn256
-
(2008)
Hum. Mol. Genet
, vol.17
, pp. 3617-3630
-
-
Royer-Zemmour, B.1
Ponsole-Lenfant, M.2
Gara, H.3
Roll, P.4
Lévêque, C.5
Massacrier, A.6
-
207
-
-
38249042915
-
NCAM: the molecule and its genetics
-
Rutishauser, U., and Goridis, C. (1986). NCAM: the molecule and its genetics. Trends Genet. 2, 72-76. doi: 10.1016/0168-9525(86)90182-4
-
(1986)
Trends Genet
, vol.2
, pp. 72-76
-
-
Rutishauser, U.1
Goridis, C.2
-
208
-
-
49049085537
-
Deletion of ERK2 mitogen-activated protein kinase identifies its key roles in cortical neurogenesis and cognitive function
-
Samuels, I. S., Karlo, J. C., Faruzzi, A. N., Pickering, K., Herrup, K., Sweatt, J. D.,et al. (2008). Deletion of ERK2 mitogen-activated protein kinase identifies its key roles in cortical neurogenesis and cognitive function. J. Neurosci. 28, 6983-6995. doi: 10.1523/JNEUROSCI.0679-08.2008
-
(2008)
J. Neurosci
, vol.28
, pp. 6983-6995
-
-
Samuels, I.S.1
Karlo, J.C.2
Faruzzi, A.N.3
Pickering, K.4
Herrup, K.5
Sweatt, J.D.6
-
209
-
-
79251587453
-
Thalamocortical pathfinding defects precede degeneration of the reticular thalamic nucleus in polysialic acid-deficient mice
-
Schiff, M., Röckle, I., Burkhardt, H., Weinhold, B., and Hildebrandt, H. (2011). Thalamocortical pathfinding defects precede degeneration of the reticular thalamic nucleus in polysialic acid-deficient mice. J. Neurosci. 31, 1302-1312. doi: 10.1523/JNEUROSCI.5609-10.2011
-
(2011)
J. Neurosci
, vol.31
, pp. 1302-1312
-
-
Schiff, M.1
Röckle, I.2
Burkhardt, H.3
Weinhold, B.4
Hildebrandt, H.5
-
210
-
-
77955279065
-
Building a bridal chamber: development of the thalamus
-
Scholpp, S., and Lumsden, A. (2010). Building a bridal chamber: development of the thalamus. Trends Neurosci. 33, 373-380. doi: 10.1016/j.tins.2010.05.003
-
(2010)
Trends Neurosci
, vol.33
, pp. 373-380
-
-
Scholpp, S.1
Lumsden, A.2
-
211
-
-
32344446690
-
Hedgehog signalling from the zona limitans intrathalamica orchestrates patterning of the zebrafish diencephalon
-
Scholpp, S., Wolf, O., Brand, M., and Lumsden, A. (2006). Hedgehog signalling from the zona limitans intrathalamica orchestrates patterning of the zebrafish diencephalon. Development 133, 855-864. doi: 10.1242/dev.02248
-
(2006)
Development
, vol.133
, pp. 855-864
-
-
Scholpp, S.1
Wolf, O.2
Brand, M.3
Lumsden, A.4
-
212
-
-
84882452116
-
Intragenic epigenetic changes modulate NCAM alternative splicing in neuronal differentiation
-
Schor, I. E., Fiszbein, A., Petrillo, E., and Kornblihtt, A. R. (2013). Intragenic epigenetic changes modulate NCAM alternative splicing in neuronal differentiation. EMBO J. 32, 2264-2274. doi: 10.1038/emboj.2013.167
-
(2013)
EMBO J
, vol.32
, pp. 2264-2274
-
-
Schor, I.E.1
Fiszbein, A.2
Petrillo, E.3
Kornblihtt, A.R.4
-
213
-
-
84907587167
-
Humanized Foxp2 accelerates learning by enhancing transitions from declarative to procedural performance
-
Schreiweis, C., Bornschein, U., Burguière, E., Kerimoglu, C., Schreiter, S., Dannemann, M.,et al. (2014). Humanized Foxp2 accelerates learning by enhancing transitions from declarative to procedural performance. Proc. Natl. Acad. Sci. U.S.A. 111, 14253-14258. doi: 10.1073/pnas.1414542111
-
(2014)
Proc. Natl. Acad. Sci. U.S.A
, vol.111
, pp. 14253-14258
-
-
Schreiweis, C.1
Bornschein, U.2
Burguière, E.3
Kerimoglu, C.4
Schreiter, S.5
Dannemann, M.6
-
214
-
-
0025923088
-
Mice homozygous for the ablm1 mutation show poor viability and depletion of selected B and T cell populations
-
Schwartzberg, P. L., Stall, A. M., Hardin, J. D., Bowdish, K. S., Humaran, T., Boast, S.,et al. (1991). Mice homozygous for the ablm1 mutation show poor viability and depletion of selected B and T cell populations. Cell 65, 1165-1175. doi: 10.1016/0092-8674(91)90012-N
-
(1991)
Cell
, vol.65
, pp. 1165-1175
-
-
Schwartzberg, P.L.1
Stall, A.M.2
Hardin, J.D.3
Bowdish, K.S.4
Humaran, T.5
Boast, S.6
-
215
-
-
78149301263
-
Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2
-
Scott-Van Zeeland, A. A., Abrahams, B. S., álvarez-Retuerto, A. I., Sonnenblick, L. I., Rudie, J. D., Ghahremani, D.,et al. (2010). Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2. Sci. Transl. Med. 2, 56ra80. doi: 10.1126/scitranslmed.3001344
-
(2010)
Sci. Transl. Med
, vol.2
, pp. 56-80
-
-
Scott-Van Zeeland, A.A.1
Abrahams, B.S.2
álvarez-Retuerto, A.I.3
Sonnenblick, L.I.4
Rudie, J.D.5
Ghahremani, D.6
-
216
-
-
84857127199
-
Pax6 expression in postmitotic neurons mediates the growth of axons in response to SFRP1.
-
Sebastián-Serrano, A., Sandonis, A., Cardozo, M., Rodríguez-Tornos, F. M., Bovolenta, P., and Nieto, M. (2012). Pax6 expression in postmitotic neurons mediates the growth of axons in response to SFRP1. PLoS ONE 7:e31590. doi: 10.1371/journal.pone.0031590
-
(2012)
PLoS ONE
, vol.7
-
-
Sebastián-Serrano, A.1
Sandonis, A.2
Cardozo, M.3
Rodríguez-Tornos, F.M.4
Bovolenta, P.5
Nieto, M.6
-
217
-
-
78649671271
-
Deletion of 7q34-q36.2 in two siblings with mental retardation, language delay, primary amenorrhea, and dysmorphic features.
-
Sehested, L. T., Møller, R. S., Bache, I., Andersen, N. B., Ullmann, R., Tommerup, N.,et al. (2010). Deletion of 7q34-q36.2 in two siblings with mental retardation, language delay, primary amenorrhea, and dysmorphic features. Am. J. Med. Genet. A 152A, 3115-31119. doi: 10.1002/ajmg.a.33476
-
(2010)
Am. J. Med. Genet. A
, vol.152 A
, pp. 3115-31119
-
-
Sehested, L.T.1
Møller, R.S.2
Bache, I.3
Andersen, N.B.4
Ullmann, R.5
Tommerup, N.6
-
218
-
-
0029371656
-
Rubinstein-Taybi syndrome: cranial MR imaging findings
-
Sener, R. N. (1995). Rubinstein-Taybi syndrome: cranial MR imaging findings. Comput. Med. Imaging. Graph. 19, 417-418. doi: 10.1016/0895-6111(95)00023-2
-
(1995)
Comput. Med. Imaging. Graph
, vol.19
, pp. 417-418
-
-
Sener, R.N.1
-
219
-
-
0035880455
-
Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females
-
Sheen, V. L., Dixon, P. H., Fox, J. W., Hong, S. E., Kinton, L., Sisodiya, S. M.,et al. (2001). Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females. Hum. Mol. Genet. 10, 1775-1783. doi: 10.1093/hmg/10.17.1775
-
(2001)
Hum. Mol. Genet
, vol.10
, pp. 1775-1783
-
-
Sheen, V.L.1
Dixon, P.H.2
Fox, J.W.3
Hong, S.E.4
Kinton, L.5
Sisodiya, S.M.6
-
220
-
-
84855464261
-
Administration of BMP2/7 in utero partially reverses Rubinstein-Taybi syndrome-like skeletal defects induced by Pdk1 or Cbp mutations in mice
-
Shim, J. H., Greenblatt, M. B., Singh, A., Brady, N., Hu, D., Drapp, R.,et al. (2012). Administration of BMP2/7 in utero partially reverses Rubinstein-Taybi syndrome-like skeletal defects induced by Pdk1 or Cbp mutations in mice. J. Clin. Invest. 122, 91-106. doi: 10.1172/JCI59466
-
(2012)
J. Clin. Invest
, vol.122
, pp. 91-106
-
-
Shim, J.H.1
Greenblatt, M.B.2
Singh, A.3
Brady, N.4
Hu, D.5
Drapp, R.6
-
221
-
-
41549140462
-
Oscillations in notch signaling regulate maintenance of neural progenitors
-
Shimojo, H., Ohtsuka, T., and Kageyama, R. (2008). Oscillations in notch signaling regulate maintenance of neural progenitors. Neuron 58, 52-64. doi: 10.1016/j.neuron.2008.02.014
-
(2008)
Neuron
, vol.58
, pp. 52-64
-
-
Shimojo, H.1
Ohtsuka, T.2
Kageyama, R.3
-
222
-
-
84879068462
-
Usf1, a suppressor of the circadian Clock mutant, reveals the nature of the DNA-binding of the CLOCK:BMAL1 complex in mice.
-
Shimomura, K., Kumar, V., Koike, N., Kim, T. K., Chong, J., Buhr, E. D.,et al. (2013). Usf1, a suppressor of the circadian Clock mutant, reveals the nature of the DNA-binding of the CLOCK:BMAL1 complex in mice. Elife 2:e00426. doi: 10.7554/eLife.00426
-
(2013)
Elife
, vol.2
-
-
Shimomura, K.1
Kumar, V.2
Koike, N.3
Kim, T.K.4
Chong, J.5
Buhr, E.D.6
-
223
-
-
33749869970
-
Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2
-
Shriberg, L. D., Ballard, K. J., Tomblin, J. B., Duffy, J. R., Odell, K. H., and Williams, C. A. (2006). Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2. J. Speech Lang. Hear. Res. 49, 500-525. doi: 10.1044/1092-4388(2006/038)
-
(2006)
J. Speech Lang. Hear. Res
, vol.49
, pp. 500-525
-
-
Shriberg, L.D.1
Ballard, K.J.2
Tomblin, J.B.3
Duffy, J.R.4
Odell, K.H.5
Williams, C.A.6
-
224
-
-
22144496080
-
Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene
-
Shu, W., Cho, J. Y., Jiang, Y., Zhang, M., Weisz, D., Elder, G. A.,et al. (2005). Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene. Proc. Natl. Acad. Sci. U.S.A. 102, 9643-9648. doi: 10.1073/pnas.0503739102
-
(2005)
Proc. Natl. Acad. Sci. U.S.A
, vol.102
, pp. 9643-9648
-
-
Shu, W.1
Cho, J.Y.2
Jiang, Y.3
Zhang, M.4
Weisz, D.5
Elder, G.A.6
-
225
-
-
0035920153
-
Characterization of a new subfamily of winged-helix/forkhead (Fox) genes that are expressed in the lung and act as transcriptional repressors
-
Shu, W., Yang, H., Zhang, L., Lu, M. M., and Morrisey, E. E. (2001). Characterization of a new subfamily of winged-helix/forkhead (Fox) genes that are expressed in the lung and act as transcriptional repressors. J. Biol. Chem. 276, 27488-27497. doi: 10.1074/jbc. M100636200
-
(2001)
J. Biol. Chem
, vol.276
, pp. 27488-27497
-
-
Shu, W.1
Yang, H.2
Zhang, L.3
Lu, M.M.4
Morrisey, E.E.5
-
226
-
-
0032533875
-
cAMP-response-element-binding-protein-binding protein (CBP) and p300 are transcriptional co-activators of early growth response factor-1 (Egr-1)
-
Silverman, E. S., Du, J., Williams, A. J., Wadgaonkar, R., Drazen, J. M., and Collins, T. (1998). cAMP-response-element-binding-protein-binding protein (CBP) and p300 are transcriptional co-activators of early growth response factor-1 (Egr-1). Biochem. J. 336, 183-189.
-
(1998)
Biochem. J.
, vol.336
, pp. 183-189
-
-
Silverman, E.S.1
Du, J.2
Williams, A.J.3
Wadgaonkar, R.4
Drazen, J.M.5
Collins, T.6
-
227
-
-
79955102373
-
Non-syndromic language delay in a child with disruption in the Protocadherin11X/Y gene pair
-
Speevak, M. D., and Farrell, S. A. (2011). Non-syndromic language delay in a child with disruption in the Protocadherin11X/Y gene pair. Am. J. Med. Genet. B Neuropsychiatr. Genet. 156, 484-489. doi: 10.1002/ajmg.b.31186
-
(2011)
Am. J. Med. Genet. B Neuropsychiatr. Genet
, vol.156
, pp. 484-489
-
-
Speevak, M.D.1
Farrell, S.A.2
-
228
-
-
36749050396
-
Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain
-
Spiteri, E., Konopka, G., Coppola, G., Bomar, J., Oldham, M., Ou, J.,et al. (2007). Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain. Am. J. Hum. Genet. 81, 1144-1157. doi: 10.1086/522237
-
(2007)
Am. J. Hum. Genet
, vol.81
, pp. 1144-1157
-
-
Spiteri, E.1
Konopka, G.2
Coppola, G.3
Bomar, J.4
Oldham, M.5
Ou, J.6
-
229
-
-
84910107464
-
Common variation near ROBO2 is associated with expressive vocabulary in infancy
-
St Pourcain, B., Cents, R. A., Whitehouse, A. J., Haworth, C. M., Davis, O. S., O'Reilly, P. F.,et al. (2014). Common variation near ROBO2 is associated with expressive vocabulary in infancy. Nat. Commun. 5:4831. doi: 10.1038/ncomms5831
-
(2014)
Nat. Commun
, vol.5
, pp. 4831
-
-
St Pourcain, B.1
Cents, R.A.2
Whitehouse, A.J.3
Haworth, C.M.4
Davis, O.S.5
O'Reilly, P.F.6
-
230
-
-
10744233099
-
Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading
-
Stein, C. M., Schick, J. H., Gerry Taylor, H., Shriberg, L. D., Millard, C., Kundtz-Kluge, A.,et al. (2004). Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading. Am. J. Hum. Genet. 74, 283-297. doi: 10.1086/381562
-
(2004)
Am. J. Hum. Genet
, vol.74
, pp. 283-297
-
-
Stein, C.M.1
Schick, J.H.2
Gerry Taylor, H.3
Shriberg, L.D.4
Millard, C.5
Kundtz-Kluge, A.6
-
231
-
-
81455123144
-
Decreased expression of axon-guidance receptors in the anterior cingulate cortex in autism
-
Suda, S., Iwata, K., Shimmura, C., Kameno, Y., Anitha, A., Thanseem, I.,et al. (2011). Decreased expression of axon-guidance receptors in the anterior cingulate cortex in autism. Mol. Autism. 2:14. doi: 10.1186/2040-2392-2-14
-
(2011)
Mol. Autism
, vol.2
, pp. 14
-
-
Suda, S.1
Iwata, K.2
Shimmura, C.3
Kameno, Y.4
Anitha, A.5
Thanseem, I.6
-
232
-
-
0037036896
-
Postsynaptic activity of metabotropic glutamate receptors in the piriform cortex
-
Sugitani, M., Sugai, T., and Onoda, N. (2002). Postsynaptic activity of metabotropic glutamate receptors in the piriform cortex. Neuroreport 13, 1473-1476. doi: 10.1097/00001756-200208070-00025
-
(2002)
Neuroreport
, vol.13
, pp. 1473-1476
-
-
Sugitani, M.1
Sugai, T.2
Onoda, N.3
-
233
-
-
38049086744
-
Hes1 stimulates transcriptional activity of Runx2 by increasing protein stabilization during osteoblast differentiation
-
Suh, J. H., Lee, H. W., Lee, J. W., and Kim, J. B. (2008). Hes1 stimulates transcriptional activity of Runx2 by increasing protein stabilization during osteoblast differentiation. Biochem. Biophys. Res. Commun. 367, 97-102. doi: 10.1016/j.bbrc.2007.12.100
-
(2008)
Biochem. Biophys. Res. Commun
, vol.367
, pp. 97-102
-
-
Suh, J.H.1
Lee, H.W.2
Lee, J.W.3
Kim, J.B.4
-
234
-
-
61449233102
-
The role of Sonic hedgehog of neural origin in thalamic differentiation in the mouse
-
Szabó, N. E., Zhao, T., Zhou, X., and álvarez-Bolado, G. (2009). The role of Sonic hedgehog of neural origin in thalamic differentiation in the mouse. J. Neurosci. 29, 2453-2466. doi: 10.1523/JNEUROSCI.4524-08.2009
-
(2009)
J. Neurosci
, vol.29
, pp. 2453-2466
-
-
Szabó, N.E.1
Zhao, T.2
Zhou, X.3
álvarez-Bolado, G.4
-
235
-
-
78651324347
-
The STRING database in 2011: functional interaction networks of proteins, globally integrated and scored
-
Szklarczyk, D., Franceschini, A., Kuhn, M., Simonovic, M., Roth, A., Mínguez, P.,et al. (2011). The STRING database in 2011: functional interaction networks of proteins, globally integrated and scored. Nucleic Acids Res. 39, D561-D568. doi: 10.1093/nar/gkq973
-
(2011)
Nucleic Acids Res
, vol.39
, pp. D561-D568
-
-
Szklarczyk, D.1
Franceschini, A.2
Kuhn, M.3
Simonovic, M.4
Roth, A.5
Mínguez, P.6
-
236
-
-
0038054082
-
Expression of Foxp2, a gene involved in speech and language, in the developing and adult striatum
-
Takahashi, K., Liu, F. C., Hirokawa, K., and Takahashi, H. (2003). Expression of Foxp2, a gene involved in speech and language, in the developing and adult striatum. J. Neurosci. Res. 73, 61-72. doi: 10.1002/jnr.10638
-
(2003)
J. Neurosci. Res
, vol.73
, pp. 61-72
-
-
Takahashi, K.1
Liu, F.C.2
Hirokawa, K.3
Takahashi, H.4
-
237
-
-
77957279149
-
DIP2 disco-interacting protein 2 homolog A (Drosophila) is a candidate receptor for follistatin-related protein/follistatin-like 1-analysis of their binding with TGF-ß superfamily proteins
-
Tanaka, M., Murakami, K., Ozaki, S., Imura, Y., Tong, X. P., Watanabe, T.,et al. (2010). DIP2 disco-interacting protein 2 homolog A (Drosophila) is a candidate receptor for follistatin-related protein/follistatin-like 1-analysis of their binding with TGF-ß superfamily proteins. FEBS J. 277, 4278-4289. doi: 10.1111/j.1742-4658.2010.07816.x
-
(2010)
FEBS J
, vol.277
, pp. 4278-4289
-
-
Tanaka, M.1
Murakami, K.2
Ozaki, S.3
Imura, Y.4
Tong, X.P.5
Watanabe, T.6
-
238
-
-
84862282188
-
Prevention of premature fusion of calvarial suture in GLI-Kruppel family member 3 (Gli3)-deficient mice by removing one allele of Runt-related transcription factor 2 (Runx2)
-
Tanimoto, Y., Veistinen, L., Alakurtti, K., Takatalo, M., and Rice, D. P. (2012). Prevention of premature fusion of calvarial suture in GLI-Kruppel family member 3 (Gli3)-deficient mice by removing one allele of Runt-related transcription factor 2 (Runx2). J. Biol. Chem. 287, 21429-21438. doi: 10.1074/jbc. M112.362145
-
(2012)
J. Biol. Chem
, vol.287
, pp. 21429-21438
-
-
Tanimoto, Y.1
Veistinen, L.2
Alakurtti, K.3
Takatalo, M.4
Rice, D.P.5
-
239
-
-
48749084615
-
The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia
-
Tapia-Páez, I., Tammimies, K., Massinen, S., Roy, A. L., and Kere, J. (2008). The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia. FASEB J. 22, 3001-3009. doi: 10.1096/fj.07-104455
-
(2008)
FASEB J
, vol.22
, pp. 3001-3009
-
-
Tapia-Páez, I.1
Tammimies, K.2
Massinen, S.3
Roy, A.L.4
Kere, J.5
-
241
-
-
59449103777
-
CCAAT/enhancer-binding protein ß promotes osteoblast differentiation by enhancing Runx2 activity with ATF4
-
Tominaga, H., Maeda, S., Hayashi, M., Takeda, S., Akira, S., Komiya, S.,et al. (2008). CCAAT/enhancer-binding protein ß promotes osteoblast differentiation by enhancing Runx2 activity with ATF4. Mol. Biol. Cell. 19, 5373-5386. doi: 10.1091/mbc. E08-03-0329
-
(2008)
Mol. Biol. Cell
, vol.19
, pp. 5373-5386
-
-
Tominaga, H.1
Maeda, S.2
Hayashi, M.3
Takeda, S.4
Akira, S.5
Komiya, S.6
-
242
-
-
3042587718
-
Interaction of filamin A with the integrin beta 7 cytoplasmic domain: role of alternative splicing and phosphorylation
-
Travis, M. A., van der Flier, A., Kammerer, R. A., Mould, A. P., Sonnenberg, A., and Humphries, M. J. (2004). Interaction of filamin A with the integrin beta 7 cytoplasmic domain: role of alternative splicing and phosphorylation. FEBS Lett. 569, 185-190. doi: 10.1016/j.febslet.2004.04.099
-
(2004)
FEBS Lett
, vol.569
, pp. 185-190
-
-
Travis, M.A.1
van der Flier, A.2
Kammerer, R.A.3
Mould, A.P.4
Sonnenberg, A.5
Humphries, M.J.6
-
243
-
-
79551508983
-
Ablation of CBP in forebrain principal neurons causes modest memory and transcriptional defects and a dramatic reduction of histone acetylation but does not affect cell viability
-
Valor, L. M., Pulopulos, M. M., Jiménez-Minchán, M., Olivares, R., Lutz, B., and Barco, A. (2011). Ablation of CBP in forebrain principal neurons causes modest memory and transcriptional defects and a dramatic reduction of histone acetylation but does not affect cell viability. J. Neurosci. 31, 1652-1663. doi: 10.1523/JNEUROSCI.4737-10.2011
-
(2011)
J. Neurosci
, vol.31
, pp. 1652-1663
-
-
Valor, L.M.1
Pulopulos, M.M.2
Jiménez-Minchán, M.3
Olivares, R.4
Lutz, B.5
Barco, A.6
-
244
-
-
13244292715
-
FOXP2 and the neuroanatomy of speech and language
-
Vargha-Khadem, F., Gadian, D. G., Copp, A., and Mishkin, M. (2005). FOXP2 and the neuroanatomy of speech and language. Nat. Rev. Neurosci. 6, 131-138. doi: 10.1038/nrn1605
-
(2005)
Nat. Rev. Neurosci
, vol.6
, pp. 131-138
-
-
Vargha-Khadem, F.1
Gadian, D.G.2
Copp, A.3
Mishkin, M.4
-
245
-
-
0028870054
-
Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder
-
Vargha-Khadem, F., Watkins, K. E., Alcock, K. J., Fletcher, P., and Passingham, R. E. (1995). Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder. Proc. Natl. Acad. Sci. U.S.A. 92, 930-933. doi: 10.1073/pnas.92.3.930
-
(1995)
Proc. Natl. Acad. Sci. U.S.A
, vol.92
, pp. 930-933
-
-
Vargha-Khadem, F.1
Watkins, K.E.2
Alcock, K.J.3
Fletcher, P.4
Passingham, R.E.5
-
246
-
-
0035214828
-
Characterization of human cleaved N-CAM and association with schizophrenia
-
Vawter, M. P., Usen, N., Thatcher, L., Ladenheim, B., Zhang, P., VanderPutten, D. M.,et al. (2001). Characterization of human cleaved N-CAM and association with schizophrenia. Exp. Neurol. 172, 29-46. doi: 10.1006/exnr.2001.7790
-
(2001)
Exp. Neurol
, vol.172
, pp. 29-46
-
-
Vawter, M.P.1
Usen, N.2
Thatcher, L.3
Ladenheim, B.4
Zhang, P.5
VanderPutten, D.M.6
-
247
-
-
57149090343
-
A functional genetic link between distinct developmental language disorders
-
Vernes, S. C., Newbury, D. F., Abrahams, B. S., Winchester, L., Nicod, J., Groszer, M.,et al. (2008). A functional genetic link between distinct developmental language disorders. N. Engl. J. Med. 359, 2337-2345. doi: 10.1056/NEJMoa0802828
-
(2008)
N. Engl. J. Med
, vol.359
, pp. 2337-2345
-
-
Vernes, S.C.1
Newbury, D.F.2
Abrahams, B.S.3
Winchester, L.4
Nicod, J.5
Groszer, M.6
-
248
-
-
79960955811
-
Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain
-
Vernes, S. C., Oliver, P. L., Spiteri, E., Lockstone, H. E., Puliyadi, R., Taylor, J. M.,et al. (2011). Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain. PLoS Genet. 7:e1002145. doi: 10.1371/journal.pgen.1002145
-
(2011)
PLoS Genet
, vol.7
-
-
Vernes, S.C.1
Oliver, P.L.2
Spiteri, E.3
Lockstone, H.E.4
Puliyadi, R.5
Taylor, J.M.6
-
249
-
-
36749013035
-
High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders
-
Vernes, S. C., Spiteri, E., Nicod, J., Groszer, M., Taylor, J. M., Davies, K. E.,et al. (2007). High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders. Am. J. Hum. Genet. 81, 1232-1250. doi: 10.1086/522238
-
(2007)
Am. J. Hum. Genet
, vol.81
, pp. 1232-1250
-
-
Vernes, S.C.1
Spiteri, E.2
Nicod, J.3
Groszer, M.4
Taylor, J.M.5
Davies, K.E.6
-
250
-
-
84896725445
-
The transcription factor Zif268/Egr1, brain plasticity, and memory
-
Veyrac, A., Besnard, A., Caboche, J., Davis, S., and Laroche, S. (2014). The transcription factor Zif268/Egr1, brain plasticity, and memory. Prog. Mol. Biol. Transl. Sci. 122, 89-129. doi: 10.1016/B978-0-12-420170-5.00004-0
-
(2014)
Prog. Mol. Biol. Transl. Sci
, vol.122
, pp. 89-129
-
-
Veyrac, A.1
Besnard, A.2
Caboche, J.3
Davis, S.4
Laroche, S.5
-
251
-
-
70449533656
-
Syndromic features and mild cognitive impairment in mice with genetic reduction on p300 activity: differential contribution of p300 and CBP to Rubinstein-Taybi syndrome etiology
-
Viosca, J., López-Atalaya, J. P., Olivares, R., Eckner, R., and Barco, A. (2010). Syndromic features and mild cognitive impairment in mice with genetic reduction on p300 activity: differential contribution of p300 and CBP to Rubinstein-Taybi syndrome etiology. Neurobiol. Dis. 37, 186-194. doi: 10.1016/j.nbd.2009.10.001
-
(2010)
Neurobiol. Dis
, vol.37
, pp. 186-194
-
-
Viosca, J.1
López-Atalaya, J.P.2
Olivares, R.3
Eckner, R.4
Barco, A.5
-
252
-
-
65549084447
-
Sonic hedgehog signaling controls thalamic progenitor identity and nuclei specification in mice
-
Vue, T. Y., Bluske, K., Alishahi, A., Yang, L. L., Koyano-Nakagawa, N., Novitch, B.,et al. (2009). Sonic hedgehog signaling controls thalamic progenitor identity and nuclei specification in mice. J. Neurosci. 29, 4484-4497. doi: 10.1523/JNEUROSCI.0656-09.2009
-
(2009)
J. Neurosci
, vol.29
, pp. 4484-4497
-
-
Vue, T.Y.1
Bluske, K.2
Alishahi, A.3
Yang, L.L.4
Koyano-Nakagawa, N.5
Novitch, B.6
-
253
-
-
84863507705
-
The DISC1 promoter: characterization and regulation by FOXP2
-
Walker, R. M., Hill, A. E., Newman, A. C., Hamilton, G., Torrance, H. S., Anderson, S. M.,et al. (2012). The DISC1 promoter: characterization and regulation by FOXP2. Hum. Mol. Genet. 21, 2862-2872. doi: 10.1093/hmg/dds111
-
(2012)
Hum. Mol. Genet
, vol.21
, pp. 2862-2872
-
-
Walker, R.M.1
Hill, A.E.2
Newman, A.C.3
Hamilton, G.4
Torrance, H.S.5
Anderson, S.M.6
-
254
-
-
13144255754
-
Alternative splicing of human NrCAM in neural and nonneural tissues
-
Wang, B., Williams, H., Du, J. S., Terrett, J., and Kenwrick, S. (1998). Alternative splicing of human NrCAM in neural and nonneural tissues. Mol. Cell. Neurosci. 10, 287-295. doi: 10.1006/mcne.1997.0658
-
(1998)
Mol. Cell. Neurosci
, vol.10
, pp. 287-295
-
-
Wang, B.1
Williams, H.2
Du, J.S.3
Terrett, J.4
Kenwrick, S.5
-
255
-
-
77950504901
-
Synchrony of thalamocortical inputs maximizes cortical reliability.
-
Wang, H. P., Spencer, D., Fellous, J. M., and Sejnowski, T. J. (2010a). Synchrony of thalamocortical inputs maximizes cortical reliability. Science 328, 106-109. doi: 10.1126/science.1183108
-
(2010)
Science
, vol.328
, pp. 106-109
-
-
Wang, H.P.1
Spencer, D.2
Fellous, J.M.3
Sejnowski, T.J.4
-
256
-
-
74049144071
-
CBP histone acetyltransferase activity regulates embryonic neural differentiation in the normal and Rubinstein-Taybi syndrome brain.
-
Wang, J., Weaver, I. C., Gauthier-Fisher, A., Wang, H., He, L., Yeomans, J.,et al. (2010b). CBP histone acetyltransferase activity regulates embryonic neural differentiation in the normal and Rubinstein-Taybi syndrome brain. Dev. Cell 18, 114-125. doi: 10.1016/j.devcel.2009.10.023
-
(2010)
Dev. Cell
, vol.18
, pp. 114-125
-
-
Wang, J.1
Weaver, I.C.2
Gauthier-Fisher, A.3
Wang, H.4
He, L.5
Yeomans, J.6
-
258
-
-
84875314671
-
PQBP1, a factor linked to intellectual disability, affects alternative splicing associated with neurite outgrowth.
-
Wang, Q., Moore, M. J., Adelmant, G., Marto, J. A., and Silver, P. A. (2013a). PQBP1, a factor linked to intellectual disability, affects alternative splicing associated with neurite outgrowth. Genes Dev. 27, 615-626. doi: 10.1101/gad.212308.112
-
(2013)
Genes Dev.
, vol.27
, pp. 615-626
-
-
Wang, Q.1
Moore, M.J.2
Adelmant, G.3
Marto, J.A.4
Silver, P.A.5
-
259
-
-
84886808853
-
Over-expression of Mash1 improves the GABAergic differentiation of bone marrow mesenchymal stem cells in vitro.
-
Wang, K., Long, Q., Jia, C., Liu, Y., Yi, X., Yang, H.,et al. (2013b). Over-expression of Mash1 improves the GABAergic differentiation of bone marrow mesenchymal stem cells in vitro. Brain Res. Bull. 99, 84-94. doi: 10.1016/j.brainresbull.2013.10.005
-
(2013)
Brain Res. Bull.
, vol.99
, pp. 84-94
-
-
Wang, K.1
Long, Q.2
Jia, C.3
Liu, Y.4
Yi, X.5
Yang, H.6
-
260
-
-
84886784309
-
Hierarchical mechanisms for direct reprogramming of fibroblasts to neurons
-
Wapinski, O. L., Vierbuchen, T., Qu, K., Lee, Q. Y., Chanda, S., Fuentes, D. R.,et al. (2013). Hierarchical mechanisms for direct reprogramming of fibroblasts to neurons. Cell 155, 621-635. doi: 10.1016/j.cell.2013.09.028
-
(2013)
Cell
, vol.155
, pp. 621-635
-
-
Wapinski, O.L.1
Vierbuchen, T.2
Qu, K.3
Lee, Q.Y.4
Chanda, S.5
Fuentes, D.R.6
-
261
-
-
0033007323
-
PQBP-1, a novel polyglutamine tract-binding protein, inhibits transcription activation by Brn-2 and affects cell survival
-
Waragai, M., Lammers, C. H., Takeuchi, S., Imafuku, I., Udagawa, Y., Kanazawa, I.,et al. (1999). PQBP-1, a novel polyglutamine tract-binding protein, inhibits transcription activation by Brn-2 and affects cell survival. Hum. Mol. Genet. 8, 977-87. doi: 10.1093/hmg/8.6.977
-
(1999)
Hum. Mol. Genet
, vol.8
, pp. 977-987
-
-
Waragai, M.1
Lammers, C.H.2
Takeuchi, S.3
Imafuku, I.4
Udagawa, Y.5
Kanazawa, I.6
-
262
-
-
0036190947
-
Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia
-
Watkins, K. E., Dronkers, N. F., and Vargha-Khadem, F. (2002). Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia. Brain 125, 452-464. doi: 10.1093/brain/awf058
-
(2002)
Brain
, vol.125
, pp. 452-464
-
-
Watkins, K.E.1
Dronkers, N.F.2
Vargha-Khadem, F.3
-
263
-
-
0037075618
-
Molecular neurobiology of human cognition
-
Weeber, E. J., and Sweatt, J. D. (2002). Molecular neurobiology of human cognition. Neuron 33, 845-848. doi: 10.1016/S0896-6273(02)00634-7
-
(2002)
Neuron
, vol.33
, pp. 845-848
-
-
Weeber, E.J.1
Sweatt, J.D.2
-
264
-
-
84879999423
-
Phenotypic and functional consequences of haploinsufficiency of genes from exocyst and retinoic acid pathway due to a recurrent microdeletion of 2p13.2
-
Wen, J., Lopes, F., Soares, G., Farrell, S. A., Nelson, C., Qiao, Y.,et al. (2013). Phenotypic and functional consequences of haploinsufficiency of genes from exocyst and retinoic acid pathway due to a recurrent microdeletion of 2p13.2. Orphanet J Rare Dis. 8:100. doi: 10.1186/1750-1172-8-100
-
(2013)
Orphanet J Rare Dis
, vol.8
, pp. 100
-
-
Wen, J.1
Lopes, F.2
Soares, G.3
Farrell, S.A.4
Nelson, C.5
Qiao, Y.6
-
265
-
-
33748943986
-
Accelerated evolution of Protocadherin11X/Y: a candidate gene-pair for cerebral asymmetry and language
-
Williams, N. A., Close, J. P., Giouzeli, M., and Crow, T. J. (2006). Accelerated evolution of Protocadherin11X/Y: a candidate gene-pair for cerebral asymmetry and language. Am. J. Med. Genet. B Neuropsychiatr. Genet. 141, 623-633. doi: 10.1002/ajmg.b.30357
-
(2006)
Am. J. Med. Genet. B Neuropsychiatr. Genet
, vol.141
, pp. 623-633
-
-
Williams, N.A.1
Close, J.P.2
Giouzeli, M.3
Crow, T.J.4
-
266
-
-
84865160657
-
HES1 opposes a PTEN-dependent check on survival, differentiation, and proliferation of TCRß-selected mouse thymocytes
-
Wong, G. W., Knowles, G. C., Mak, T. W., Ferrando, A. A., and Zúñiga-Pflücker, J. C. (2012). HES1 opposes a PTEN-dependent check on survival, differentiation, and proliferation of TCRß-selected mouse thymocytes. Blood 120, 1439-1448. doi: 10.1182/blood-2011-12-395319
-
(2012)
Blood
, vol.120
, pp. 1439-1448
-
-
Wong, G.W.1
Knowles, G.C.2
Mak, T.W.3
Ferrando, A.A.4
Zúñiga-Pflücker, J.C.5
-
268
-
-
0035912244
-
The neuronal repellent Slit inhibits leukocyte chemotaxis induced by chemotactic factors
-
Wu, J. Y., Feng, L., Park, H. T., Havlioglu, N., Wen, L., Tang, H.,et al. (2001). The neuronal repellent Slit inhibits leukocyte chemotaxis induced by chemotactic factors. Nature 410, 948-952. doi: 10.1038/35073616
-
(2001)
Nature
, vol.410
, pp. 948-952
-
-
Wu, J.Y.1
Feng, L.2
Park, H.T.3
Havlioglu, N.4
Wen, L.5
Tang, H.6
-
269
-
-
0141426629
-
Activated Cdc42 sequesters c-Cbl and prevents EGF receptor degradation
-
Wu, W. J., Tu, S., and Cerione, R. A. (2003). Activated Cdc42 sequesters c-Cbl and prevents EGF receptor degradation. Cell 114, 715-725. doi: 10.1016/S0092-8674(03)00688-3
-
(2003)
Cell
, vol.114
, pp. 715-725
-
-
Wu, W.J.1
Tu, S.2
Cerione, R.A.3
-
270
-
-
2442500635
-
AML1 is functionally regulated through p300-mediated acetylation on specific lysine residues
-
Yamaguchi, Y., Kurokawa, M., Imai, Y., Izutsu, K., Asai, T., Ichikawa, M.,et al. (2004). AML1 is functionally regulated through p300-mediated acetylation on specific lysine residues. J. Biol. Chem. 279, 15630-15638. doi: 10.1074/jbc. M400355200
-
(2004)
J. Biol. Chem
, vol.279
, pp. 15630-15638
-
-
Yamaguchi, Y.1
Kurokawa, M.2
Imai, Y.3
Izutsu, K.4
Asai, T.5
Ichikawa, M.6
-
271
-
-
77953963335
-
The mouse forkhead gene Foxp2 modulates expression of the lung genes.
-
Yang, Z., Hikosaka, K., Sharkar, M. T., Tamakoshi, T., Chandra, A., Wang, B.,et al. (2010a). The mouse forkhead gene Foxp2 modulates expression of the lung genes. Life Sci. 87, 17-25. doi: 10.1016/j.lfs.2010.05.009
-
(2010)
Life Sci.
, vol.87
, pp. 17-25
-
-
Yang, Z.1
Hikosaka, K.2
Sharkar, M.T.3
Tamakoshi, T.4
Chandra, A.5
Wang, B.6
-
272
-
-
76749162906
-
The dynamic ubiquitin ligase duo: Cdh1-APC and Cdc20-APC regulate neuronal morphogenesis and connectivity.
-
Yang, Y., Kim, A. H., and Bonni, A. (2010b). The dynamic ubiquitin ligase duo: Cdh1-APC and Cdc20-APC regulate neuronal morphogenesis and connectivity. Curr. Opin. Neurobiol. 20, 92-99. doi: 10.1016/j.conb.2009.12.004
-
(2010)
Curr. Opin. Neurobiol.
, vol.20
, pp. 92-99
-
-
Yang, Y.1
Kim, A.H.2
Bonni, A.3
-
273
-
-
73249126948
-
Slit2 inhibits glioma cell invasion in the brain by suppression of Cdc42 activity
-
Yiin, J. J., Hu, B., Jarzynka, M. J., Feng, H., Liu, K. W., Wu, J. Y.,et al. (2009). Slit2 inhibits glioma cell invasion in the brain by suppression of Cdc42 activity. Neuro. Oncol. 11, 779-789. doi: 10.1215/15228517-2009-017
-
(2009)
Neuro. Oncol
, vol.11
, pp. 779-789
-
-
Yiin, J.J.1
Hu, B.2
Jarzynka, M.J.3
Feng, H.4
Liu, K.W.5
Wu, J.Y.6
-
274
-
-
0035944532
-
Evidence that GRIP, a PDZ-domain protein which is expressed in the embryonic forebrain, co-activates transcription with DLX homeodomain proteins
-
Yu, G., Zerucha, T., Ekker, M., and Rubenstein, J. L. (2001). Evidence that GRIP, a PDZ-domain protein which is expressed in the embryonic forebrain, co-activates transcription with DLX homeodomain proteins. Brain Res. Dev. Brain Res. 130, 217-230. doi: 10.1016/S0165-3806(01)00239-5
-
(2001)
Brain Res. Dev. Brain Res
, vol.130
, pp. 217-230
-
-
Yu, G.1
Zerucha, T.2
Ekker, M.3
Rubenstein, J.L.4
-
275
-
-
0242497936
-
Specific interaction of Egr1 and c/EBPß leads to the transcriptional activation of the human low density lipoprotein receptor gene
-
Zhang, F., Lin, M., Abidi, P., Thiel, G., and Liu, J. (2003). Specific interaction of Egr1 and c/EBPß leads to the transcriptional activation of the human low density lipoprotein receptor gene. J. Biol. Chem. 278, 44246-44254. doi: 10.1074/jbc. M305564200
-
(2003)
J. Biol. Chem
, vol.278
, pp. 44246-44254
-
-
Zhang, F.1
Lin, M.2
Abidi, P.3
Thiel, G.4
Liu, J.5
-
276
-
-
79960107144
-
Pathway-based association analyses identified TRAIL pathway for osteoporotic fractures.
-
Zhang, Y. P., Liu, Y. Z., Guo, Y., Liu, X. G., Xu, X. H., Guo, Y. F.,et al. (2011). Pathway-based association analyses identified TRAIL pathway for osteoporotic fractures. PLoS ONE 6:e21835. doi: 10.1371/journal.pone.0021835
-
(2011)
PLoS ONE
, vol.6
-
-
Zhang, Y.P.1
Liu, Y.Z.2
Guo, Y.3
Liu, X.G.4
Xu, X.H.5
Guo, Y.F.6
-
277
-
-
84865097353
-
P38 and ERK1/2 MAPKs act in opposition to regulate BMP9-induced osteogenic differentiation of mesenchymal progenitor cells.
-
Zhao, Y., Song, T., Wang, W., Wang, J., He, J., Wu, N.,et al. (2012). P38 and ERK1/2 MAPKs act in opposition to regulate BMP9-induced osteogenic differentiation of mesenchymal progenitor cells. PLoS ONE 7:e43383. doi: 10.1371/journal.pone.0043383
-
(2012)
PLoS ONE
, vol.7
-
-
Zhao, Y.1
Song, T.2
Wang, W.3
Wang, J.4
He, J.5
Wu, N.6
-
278
-
-
45249124700
-
Foxp2 inhibits Nkx2.1-mediated transcription of SP-C via interactions with the Nkx2.1 homeodomain
-
Zhou, B., Zhong, Q., Minoo, P., Li, C., Ann, D. K., Frenkel, B.,et al. (2008). Foxp2 inhibits Nkx2.1-mediated transcription of SP-C via interactions with the Nkx2.1 homeodomain. Am. J. Respir. Cell Mol. Biol. 38, 750-758. doi: 10.1165/rcmb.2007-0350OC
-
(2008)
Am. J. Respir. Cell Mol. Biol
, vol.38
, pp. 750-758
-
-
Zhou, B.1
Zhong, Q.2
Minoo, P.3
Li, C.4
Ann, D.K.5
Frenkel, B.6
-
279
-
-
0027510084
-
Nodal is a novel TGF-beta-like gene expressed in the mouse node during gastrulation
-
Zhou, X., Sasaki, H., Lowe, L., Hogan, B. L. M., and Kuehn, M. R. (1993). Nodal is a novel TGF-beta-like gene expressed in the mouse node during gastrulation. Nature 361, 543-547.
-
(1993)
Nature
, vol.361
, pp. 543-547
-
-
Zhou, X.1
Sasaki, H.2
Lowe, L.3
Hogan, B.L.M.4
Kuehn, M.R.5
|