-
1
-
-
76649086962
-
Neuroligin-1 deletion results in impaired spatial memory and increased repetitive behavior
-
Blundell J., Blaiss C.A., Etherton M.R., Espinosa F., Tabuchi K., Walz C., Bolliger M.F., Südhof T.C., Powell C.M. Neuroligin-1 deletion results in impaired spatial memory and increased repetitive behavior. J.Neurosci. 2010, 30:2115-2129.
-
(2010)
J.Neurosci.
, vol.30
, pp. 2115-2129
-
-
Blundell, J.1
Blaiss, C.A.2
Etherton, M.R.3
Espinosa, F.4
Tabuchi, K.5
Walz, C.6
Bolliger, M.F.7
Südhof, T.C.8
Powell, C.M.9
-
2
-
-
26944444692
-
A splice code for trans-synaptic cell adhesion mediated by binding of neuroligin 1 to alpha- and beta-neurexins
-
Boucard A.A., Chubykin A.A., Comoletti D., Taylor P., Südhof T.C. A splice code for trans-synaptic cell adhesion mediated by binding of neuroligin 1 to alpha- and beta-neurexins. Neuron 2005, 48:229-236.
-
(2005)
Neuron
, vol.48
, pp. 229-236
-
-
Boucard, A.A.1
Chubykin, A.A.2
Comoletti, D.3
Taylor, P.4
Südhof, T.C.5
-
3
-
-
0032544613
-
A tripartite protein complex with the potential to couple synaptic vesicle exocytosis to cell adhesion in brain
-
Butz S., Okamoto M., Südhof T.C. A tripartite protein complex with the potential to couple synaptic vesicle exocytosis to cell adhesion in brain. Cell 1998, 94:773-782.
-
(1998)
Cell
, vol.94
, pp. 773-782
-
-
Butz, S.1
Okamoto, M.2
Südhof, T.C.3
-
4
-
-
84861230108
-
Mutations affecting synaptic levels of neurexin-1β in autism and mental retardation
-
Camacho-Garcia R.J., Planelles M.I., Margalef M., Pecero M.L., Martínez-Leal R., Aguilera F., Vilella E., Martinez-Mir A., Scholl F.G. Mutations affecting synaptic levels of neurexin-1β in autism and mental retardation. Neurobiol. Dis. 2012, 47:135-143.
-
(2012)
Neurobiol. Dis.
, vol.47
, pp. 135-143
-
-
Camacho-Garcia, R.J.1
Planelles, M.I.2
Margalef, M.3
Pecero, M.L.4
Martínez-Leal, R.5
Aguilera, F.6
Vilella, E.7
Martinez-Mir, A.8
Scholl, F.G.9
-
5
-
-
84887090057
-
Rare variants analysis of neurexin-1β inautism reveals a novel start codon mutation affecting protein levels at synapses
-
Camacho-Garcia R.J., Hervás A., Toma C., Balmaña N., Cormand B., Martinez-Mir A., Scholl F.G. Rare variants analysis of neurexin-1β inautism reveals a novel start codon mutation affecting protein levels at synapses. Psychiatr. Genet. 2013, 23:262-266.
-
(2013)
Psychiatr. Genet.
, vol.23
, pp. 262-266
-
-
Camacho-Garcia, R.J.1
Hervás, A.2
Toma, C.3
Balmaña, N.4
Cormand, B.5
Martinez-Mir, A.6
Scholl, F.G.7
-
6
-
-
0035093830
-
Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
-
Chen R.Z., Akbarian S., Tudor M., Jaenisch R. Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice. Nat. Genet. 2001, 27:327-331.
-
(2001)
Nat. Genet.
, vol.27
, pp. 327-331
-
-
Chen, R.Z.1
Akbarian, S.2
Tudor, M.3
Jaenisch, R.4
-
7
-
-
77952691843
-
Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders
-
Children's Hospital Boston Genotype Phenotype Study Group
-
Ching M.S., Shen Y., Tan W.H., Jeste S.S., Morrow E.M., Chen X., Mukaddes N.M., Yoo S.Y., Hanson E., Hundley R., et al. Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders. Am. J. Med. Genet. B. Neuropsychiatr. Genet. 2010, 153B:937-947. Children's Hospital Boston Genotype Phenotype Study Group.
-
(2010)
Am. J. Med. Genet. B. Neuropsychiatr. Genet.
, vol.153 B
, pp. 937-947
-
-
Ching, M.S.1
Shen, Y.2
Tan, W.H.3
Jeste, S.S.4
Morrow, E.M.5
Chen, X.6
Mukaddes, N.M.7
Yoo, S.Y.8
Hanson, E.9
Hundley, R.10
-
8
-
-
79955672523
-
Neurexin-neuroligin transsynaptic interaction mediates learning-related synaptic remodeling and long-term facilitation in aplysia
-
Choi Y.B., Li H.L., Kassabov S.R., Jin I., Puthanveettil S.V., Karl K.A., Lu Y., Kim J.H., Bailey C.H., Kandel E.R. Neurexin-neuroligin transsynaptic interaction mediates learning-related synaptic remodeling and long-term facilitation in aplysia. Neuron 2011, 70:468-481.
-
(2011)
Neuron
, vol.70
, pp. 468-481
-
-
Choi, Y.B.1
Li, H.L.2
Kassabov, S.R.3
Jin, I.4
Puthanveettil, S.V.5
Karl, K.A.6
Lu, Y.7
Kim, J.H.8
Bailey, C.H.9
Kandel, E.R.10
-
9
-
-
33750348559
-
Gene selection, alternative splicing, and post-translational processing regulate neuroligin selectivity for beta-neurexins
-
Comoletti D., Flynn R.E., Boucard A.A., Demeler B., Schirf V., Shi J., Jennings L.L., Newlin H.R., Südhof T.C., Taylor P. Gene selection, alternative splicing, and post-translational processing regulate neuroligin selectivity for beta-neurexins. Biochemistry 2006, 45:12816-12827.
-
(2006)
Biochemistry
, vol.45
, pp. 12816-12827
-
-
Comoletti, D.1
Flynn, R.E.2
Boucard, A.A.3
Demeler, B.4
Schirf, V.5
Shi, J.6
Jennings, L.L.7
Newlin, H.R.8
Südhof, T.C.9
Taylor, P.10
-
10
-
-
0037743572
-
Neurexin mediates the assembly of presynaptic terminals
-
Dean C., Scholl F.G., Choih J., DeMaria S., Berger J., Isacoff E., Scheiffele P. Neurexin mediates the assembly of presynaptic terminals. Nat. Neurosci. 2003, 6:708-716.
-
(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
Scheiffele, P.7
-
11
-
-
33845889998
-
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
-
Durand C.M., Betancur C., Boeckers T.M., Bockmann J., Chaste P., Fauchereau F., Nygren G., Rastam M., Gillberg I.C., Anckarsäter H., et al. Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders. Nat. Genet. 2007, 39:25-27.
-
(2007)
Nat. Genet.
, vol.39
, pp. 25-27
-
-
Durand, C.M.1
Betancur, C.2
Boeckers, T.M.3
Bockmann, J.4
Chaste, P.5
Fauchereau, F.6
Nygren, G.7
Rastam, M.8
Gillberg, I.C.9
Anckarsäter, H.10
-
12
-
-
84876854542
-
The tissue-specific RNA binding protein T-STAR controls regional splicing patterns of neurexin pre-mRNAs in the brain
-
Ehrmann I., Dalgliesh C., Liu Y., Danilenko M., Crosier M., Overman L., Arthur H.M., Lindsay S., Clowry G.J., Venables J.P., et al. The tissue-specific RNA binding protein T-STAR controls regional splicing patterns of neurexin pre-mRNAs in the brain. PLoS Genet. 2013, 9:e1003474.
-
(2013)
PLoS Genet.
, vol.9
-
-
Ehrmann, I.1
Dalgliesh, C.2
Liu, Y.3
Danilenko, M.4
Crosier, M.5
Overman, L.6
Arthur, H.M.7
Lindsay, S.8
Clowry, G.J.9
Venables, J.P.10
-
13
-
-
70449686185
-
Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments
-
Etherton M.R., Blaiss C.A., Powell C.M., Südhof T.C. Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments. Proc. Natl. Acad. Sci. USA 2009, 106:17998-18003.
-
(2009)
Proc. Natl. Acad. Sci. USA
, vol.106
, pp. 17998-18003
-
-
Etherton, M.R.1
Blaiss, C.A.2
Powell, C.M.3
Südhof, T.C.4
-
14
-
-
58149395699
-
Polarized targeting of neurexins to synapses is regulated by their C-terminal sequences
-
Fairless R., Masius H., Rohlmann A., Heupel K., Ahmad M., Reissner C., Dresbach T., Missler M. Polarized targeting of neurexins to synapses is regulated by their C-terminal sequences. J.Neurosci. 2008, 28:12969-12981.
-
(2008)
J.Neurosci.
, vol.28
, pp. 12969-12981
-
-
Fairless, R.1
Masius, H.2
Rohlmann, A.3
Heupel, K.4
Ahmad, M.5
Reissner, C.6
Dresbach, T.7
Missler, M.8
-
15
-
-
33846564563
-
Retrograde modulation of presynaptic release probability through signaling mediated by PSD-95-neuroligin
-
Futai K., Kim M.J., Hashikawa T., Scheiffele P., Sheng M., Hayashi Y. Retrograde modulation of presynaptic release probability through signaling mediated by PSD-95-neuroligin. Nat. Neurosci. 2007, 10:186-195.
-
(2007)
Nat. Neurosci.
, vol.10
, pp. 186-195
-
-
Futai, K.1
Kim, M.J.2
Hashikawa, T.3
Scheiffele, P.4
Sheng, M.5
Hayashi, Y.6
-
16
-
-
80054860297
-
Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia
-
Gauthier J., Siddiqui T.J., Huashan P., Yokomaku D., Hamdan F.F., Champagne N., Lapointe M., Spiegelman D., Noreau A., Lafrenière R.G., et al. Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia. Hum. Genet. 2011, 130:563-573.
-
(2011)
Hum. Genet.
, vol.130
, pp. 563-573
-
-
Gauthier, J.1
Siddiqui, T.J.2
Huashan, P.3
Yokomaku, D.4
Hamdan, F.F.5
Champagne, N.6
Lapointe, M.7
Spiegelman, D.8
Noreau, A.9
Lafrenière, R.G.10
-
17
-
-
84872595085
-
Autism-related deficits via dysregulated eIF4E-dependent translational control
-
Gkogkas C.G., Khoutorsky A., Ran I., Rampakakis E., Nevarko T., Weatherill D.B., Vasuta C., Yee S., Truitt M., Dallaire P., et al. Autism-related deficits via dysregulated eIF4E-dependent translational control. Nature 2013, 493:371-377.
-
(2013)
Nature
, vol.493
, pp. 371-377
-
-
Gkogkas, C.G.1
Khoutorsky, A.2
Ran, I.3
Rampakakis, E.4
Nevarko, T.5
Weatherill, D.B.6
Vasuta, C.7
Yee, S.8
Truitt, M.9
Dallaire, P.10
-
18
-
-
84883387704
-
Membrane-tethered monomeric neurexin LNS-domain triggers synapse formation
-
Gokce O., Südhof T.C. Membrane-tethered monomeric neurexin LNS-domain triggers synapse formation. J.Neurosci. 2013, 33:14617-14628.
-
(2013)
J.Neurosci.
, vol.33
, pp. 14617-14628
-
-
Gokce, O.1
Südhof, T.C.2
-
19
-
-
33748576937
-
Clathrin-mediated endocytosis is the dominant mechanism of vesicle retrieval at hippocampal synapses
-
Granseth B., Odermatt B., Royle S.J., Lagnado L. Clathrin-mediated endocytosis is the dominant mechanism of vesicle retrieval at hippocampal synapses. Neuron 2006, 51:773-786.
-
(2006)
Neuron
, vol.51
, pp. 773-786
-
-
Granseth, B.1
Odermatt, B.2
Royle, S.J.3
Lagnado, L.4
-
20
-
-
84879522237
-
Altered social behaviours in neurexin 1α knockout mice resemble core symptoms in neurodevelopmental disorders
-
Grayton H.M., Missler M., Collier D.A., Fernandes C. Altered social behaviours in neurexin 1α knockout mice resemble core symptoms in neurodevelopmental disorders. PLoS ONE 2013, 8:e67114.
-
(2013)
PLoS ONE
, vol.8
-
-
Grayton, H.M.1
Missler, M.2
Collier, D.A.3
Fernandes, C.4
-
21
-
-
33847266846
-
Reversal of neurological defects in a mouse model of Rett syndrome
-
Guy J., Gan J., Selfridge J., Cobb S., Bird A. Reversal of neurological defects in a mouse model of Rett syndrome. Science 2007, 315:1143-1147.
-
(2007)
Science
, vol.315
, pp. 1143-1147
-
-
Guy, J.1
Gan, J.2
Selfridge, J.3
Cobb, S.4
Bird, A.5
-
22
-
-
84455200617
-
SAM68 regulates neuronal activity-dependent alternative splicing of neurexin-1
-
Iijima T., Wu K., Witte H., Hanno-Iijima Y., Glatter T., Richard S., Scheiffele P. SAM68 regulates neuronal activity-dependent alternative splicing of neurexin-1. Cell 2011, 147:1601-1614.
-
(2011)
Cell
, vol.147
, pp. 1601-1614
-
-
Iijima, T.1
Wu, K.2
Witte, H.3
Hanno-Iijima, Y.4
Glatter, T.5
Richard, S.6
Scheiffele, P.7
-
23
-
-
0037656313
-
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
-
Paris Autism Research International Sibpair Study
-
Jamain S., Quach H., Betancur C., Råstam M., Colineaux C., Gillberg I.C., Soderstrom H., Giros B., Leboyer M., Gillberg C., Bourgeron T. Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. Nat. Genet. 2003, 34:27-29. Paris Autism Research International Sibpair Study.
-
(2003)
Nat. Genet.
, vol.34
, pp. 27-29
-
-
Jamain, S.1
Quach, H.2
Betancur, C.3
Råstam, M.4
Colineaux, C.5
Gillberg, I.C.6
Soderstrom, H.7
Giros, B.8
Leboyer, M.9
Gillberg, C.10
Bourgeron, T.11
-
24
-
-
33646142995
-
Pten regulates neuronal arborization and social interaction in mice
-
Kwon C.H., Luikart B.W., Powell C.M., Zhou J., Matheny S.A., Zhang W., Li Y., Baker S.J., Parada L.F. Pten regulates neuronal arborization and social interaction in mice. Neuron 2006, 50:377-388.
-
(2006)
Neuron
, vol.50
, pp. 377-388
-
-
Kwon, C.H.1
Luikart, B.W.2
Powell, C.M.3
Zhou, J.4
Matheny, S.A.5
Zhang, W.6
Li, Y.7
Baker, S.J.8
Parada, L.F.9
-
25
-
-
84862898614
-
Activity-dependent regulation of inhibition via GAD67
-
Lau C.G., Murthy V.N. Activity-dependent regulation of inhibition via GAD67. J.Neurosci. 2012, 32:8521-8531.
-
(2012)
J.Neurosci.
, vol.32
, pp. 8521-8531
-
-
Lau, C.G.1
Murthy, V.N.2
-
26
-
-
12144291350
-
X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family
-
Laumonnier F., Bonnet-Brilhault F., Gomot M., Blanc R., David A., Moizard M.P., Raynaud M., Ronce N., Lemonnier E., Calvas P., et al. X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family. Am. J. Hum. Genet. 2004, 74:552-557.
-
(2004)
Am. J. Hum. Genet.
, vol.74
, pp. 552-557
-
-
Laumonnier, F.1
Bonnet-Brilhault, F.2
Gomot, M.3
Blanc, R.4
David, A.5
Moizard, M.P.6
Raynaud, M.7
Ronce, N.8
Lemonnier, E.9
Calvas, P.10
-
28
-
-
0029807527
-
Control of memory formation through regulated expression of a CaMKII transgene
-
Mayford M., Bach M.E., Huang Y.Y., Wang L., Hawkins R.D., Kandel E.R. Control of memory formation through regulated expression of a CaMKII transgene. Science 1996, 274:1678-1683.
-
(1996)
Science
, vol.274
, pp. 1678-1683
-
-
Mayford, M.1
Bach, M.E.2
Huang, Y.Y.3
Wang, L.4
Hawkins, R.D.5
Kandel, E.R.6
-
30
-
-
0037774700
-
Alpha-neurexins couple Ca2+ channels to synaptic vesicle exocytosis
-
Missler M., Zhang W., Rohlmann A., Kattenstroth G., Hammer R.E., Gottmann K., Südhof T.C. Alpha-neurexins couple Ca2+ channels to synaptic vesicle exocytosis. Nature 2003, 423:939-948.
-
(2003)
Nature
, vol.423
, pp. 939-948
-
-
Missler, M.1
Zhang, W.2
Rohlmann, A.3
Kattenstroth, G.4
Hammer, R.E.5
Gottmann, K.6
Südhof, T.C.7
-
31
-
-
84889561601
-
Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism
-
Parikshak N.N., Luo R., Zhang A., Won H., Lowe J.K., Chandran V., Horvath S., Geschwind D.H. Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism. Cell 2013, 155:1008-1021.
-
(2013)
Cell
, vol.155
, pp. 1008-1021
-
-
Parikshak, N.N.1
Luo, R.2
Zhang, A.3
Won, H.4
Lowe, J.K.5
Chandran, V.6
Horvath, S.7
Geschwind, D.H.8
-
32
-
-
80053540965
-
Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits
-
Peñagarikano O., Abrahams B.S., Herman E.I., Winden K.D., Gdalyahu A., Dong H., Sonnenblick L.I., Gruver R., Almajano J., Bragin A., et al. Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits. Cell 2011, 147:235-246.
-
(2011)
Cell
, vol.147
, pp. 235-246
-
-
Peñagarikano, O.1
Abrahams, B.S.2
Herman, E.I.3
Winden, K.D.4
Gdalyahu, A.5
Dong, H.6
Sonnenblick, L.I.7
Gruver, R.8
Almajano, J.9
Bragin, A.10
-
33
-
-
0028958250
-
Neurexins are differentially expressed in the embryonic nervous system of mice
-
Püschel A.W., Betz H. Neurexins are differentially expressed in the embryonic nervous system of mice. J.Neurosci. 1995, 15:2849-2856.
-
(1995)
J.Neurosci.
, vol.15
, pp. 2849-2856
-
-
Püschel, A.W.1
Betz, H.2
-
34
-
-
84869235517
-
Phenotypic spectrum and genotype-phenotype correlations of NRXN1 exon deletions
-
Schaaf C.P., Boone P.M., Sampath S., Williams C., Bader P.I., Mueller J.M., Shchelochkov O.A., Brown C.W., Crawford H.P., Phalen J.A., et al. Phenotypic spectrum and genotype-phenotype correlations of NRXN1 exon deletions. Eur. J. Hum. Genet. 2012, 20:1240-1247.
-
(2012)
Eur. J. Hum. Genet.
, vol.20
, pp. 1240-1247
-
-
Schaaf, C.P.1
Boone, P.M.2
Sampath, S.3
Williams, C.4
Bader, P.I.5
Mueller, J.M.6
Shchelochkov, O.A.7
Brown, C.W.8
Crawford, H.P.9
Phalen, J.A.10
-
35
-
-
0034625250
-
Neuroligin expressed in nonneuronal cells triggers presynaptic development in contacting axons
-
Scheiffele P., Fan J., Choih J., Fetter R., Serafini T. Neuroligin expressed in nonneuronal cells triggers presynaptic development in contacting axons. Cell 2000, 101:657-669.
-
(2000)
Cell
, vol.101
, pp. 657-669
-
-
Scheiffele, P.1
Fan, J.2
Choih, J.3
Fetter, R.4
Serafini, T.5
-
36
-
-
84875478700
-
Corticostriatal connectivity and its role in disease
-
Shepherd G.M. Corticostriatal connectivity and its role in disease. Nat. Rev. Neurosci. 2013, 14:278-291.
-
(2013)
Nat. Rev. Neurosci.
, vol.14
, pp. 278-291
-
-
Shepherd, G.M.1
-
37
-
-
77953800799
-
Behavioural phenotyping assays for mouse models of autism
-
Silverman J.L., Yang M., Lord C., Crawley J.N. Behavioural phenotyping assays for mouse models of autism. Nat. Rev. Neurosci. 2010, 11:490-502.
-
(2010)
Nat. Rev. Neurosci.
, vol.11
, pp. 490-502
-
-
Silverman, J.L.1
Yang, M.2
Lord, C.3
Crawley, J.N.4
-
38
-
-
54049091941
-
Neuroligins and neurexins link synaptic function to cognitive disease
-
Südhof T.C. Neuroligins and neurexins link synaptic function to cognitive disease. Nature 2008, 455:903-911.
-
(2008)
Nature
, vol.455
, pp. 903-911
-
-
Südhof, T.C.1
-
39
-
-
33847327313
-
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
-
Autism Genome Project Consortium
-
Szatmari P., Paterson A.D., Zwaigenbaum L., Roberts W., Brian J., Liu X.Q., Vincent J.B., Skaug J.L., Thompson A.P., Senman L., et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat. Genet. 2007, 39:319-328. Autism Genome Project Consortium.
-
(2007)
Nat. Genet.
, vol.39
, pp. 319-328
-
-
Szatmari, P.1
Paterson, A.D.2
Zwaigenbaum, L.3
Roberts, W.4
Brian, J.5
Liu, X.Q.6
Vincent, J.B.7
Skaug, J.L.8
Thompson, A.P.9
Senman, L.10
-
40
-
-
0036270811
-
Structure and evolution of neurexingenes: insight into the mechanism of alternative splicing
-
Tabuchi K., Südhof T.C. Structure and evolution of neurexingenes: insight into the mechanism of alternative splicing. Genomics 2002, 79:849-859.
-
(2002)
Genomics
, vol.79
, pp. 849-859
-
-
Tabuchi, K.1
Südhof, T.C.2
-
41
-
-
84897528076
-
Cartography of neurexin alternative splicing mapped by single-molecule long-read mRNA sequencing
-
Treutlein B., Gokce O., Quake S.R., Südhof T.C. Cartography of neurexin alternative splicing mapped by single-molecule long-read mRNA sequencing. Proc. Natl. Acad. Sci. USA 2014, 111:E1291-E1299.
-
(2014)
Proc. Natl. Acad. Sci. USA
, vol.111
-
-
Treutlein, B.1
Gokce, O.2
Quake, S.R.3
Südhof, T.C.4
-
42
-
-
84865508373
-
Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice
-
Tsai P.T., Hull C., Chu Y., Greene-Colozzi E., Sadowski A.R., Leech J.M., Steinberg J., Crawley J.N., Regehr W.G., Sahin M. Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice. Nature 2012, 488:647-651.
-
(2012)
Nature
, vol.488
, pp. 647-651
-
-
Tsai, P.T.1
Hull, C.2
Chu, Y.3
Greene-Colozzi, E.4
Sadowski, A.R.5
Leech, J.M.6
Steinberg, J.7
Crawley, J.N.8
Regehr, W.G.9
Sahin, M.10
-
43
-
-
0026769035
-
Neurexins: synaptic cell surface proteins related to the alpha-latrotoxin receptor and laminin
-
Ushkaryov Y.A., Petrenko A.G., Geppert M., Südhof T.C. Neurexins: synaptic cell surface proteins related to the alpha-latrotoxin receptor and laminin. Science 1992, 257:50-56.
-
(1992)
Science
, vol.257
, pp. 50-56
-
-
Ushkaryov, Y.A.1
Petrenko, A.G.2
Geppert, M.3
Südhof, T.C.4
-
44
-
-
84889583293
-
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism
-
Willsey A.J., Sanders S.J., Li M., Dong S., Tebbenkamp A.T., Muhle R.A., Reilly S.K., Lin L., Fertuzinhos S., Miller J.A., et al. Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. Cell 2013, 155:997-1007.
-
(2013)
Cell
, vol.155
, pp. 997-1007
-
-
Willsey, A.J.1
Sanders, S.J.2
Li, M.3
Dong, S.4
Tebbenkamp, A.T.5
Muhle, R.A.6
Reilly, S.K.7
Lin, L.8
Fertuzinhos, S.9
Miller, J.A.10
-
45
-
-
77954381448
-
Intragenic rearrangements in NRXN1 in three families with autism spectrum disorder, developmental delay, and speech delay
-
Wiśniowiecka-Kowalnik B., Nesteruk M., Peters S.U., Xia Z., Cooper M.L., Savage S., Amato R.S., Bader P., Browning M.F., Haun C.L., et al. Intragenic rearrangements in NRXN1 in three families with autism spectrum disorder, developmental delay, and speech delay. Am. J. Med. Genet. B. Neuropsychiatr. Genet. 2010, 153B:983-993.
-
(2010)
Am. J. Med. Genet. B. Neuropsychiatr. Genet.
, vol.153 B
, pp. 983-993
-
-
Wiśniowiecka-Kowalnik, B.1
Nesteruk, M.2
Peters, S.U.3
Xia, Z.4
Cooper, M.L.5
Savage, S.6
Amato, R.S.7
Bader, P.8
Browning, M.F.9
Haun, C.L.10
-
46
-
-
84862297282
-
Autistic-like social behaviour in Shank2-mutant mice improved by restoring NMDA receptor function
-
Won H., Lee H.R., Gee H.Y., Mah W., Kim J.I., Lee J., Ha S., Chung C., Jung E.S., Cho Y.S., et al. Autistic-like social behaviour in Shank2-mutant mice improved by restoring NMDA receptor function. Nature 2012, 486:261-265.
-
(2012)
Nature
, vol.486
, pp. 261-265
-
-
Won, H.1
Lee, H.R.2
Gee, H.Y.3
Mah, W.4
Kim, J.I.5
Lee, J.6
Ha, S.7
Chung, C.8
Jung, E.S.9
Cho, Y.S.10
-
47
-
-
67749118329
-
Simple behavioral assessment of mouse olfaction
-
(New York: John Wiley & Sons), Chapter 8, Unit 8.24.
-
Yang, M., and Crawley, J.N. (2009). Simple behavioral assessment of mouse olfaction. Curr. Protoc. Neurosci. (New York: John Wiley & Sons), Chapter 8, Unit 8.24.
-
(2009)
Curr. Protoc. Neurosci.
-
-
Yang, M.1
Crawley, J.N.2
-
48
-
-
84255209293
-
Automated three-chambered social approach task for mice
-
(New York: John Wiley & Sons), Chapter 8, Unit 8.26.
-
Yang, M., Silverman, J.L., and Crawley, J.N. (2011). Automated three-chambered social approach task for mice. Curr. Protoc. Neurosci. (New York: John Wiley & Sons), Chapter 8, Unit 8.26.
-
(2011)
Curr. Protoc. Neurosci
-
-
Yang, M.1
Silverman, J.L.2
Crawley, J.N.3
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