-
1
-
-
18244383565
-
Distinct phenotypes distinguish the molecular classes of Angelman syndrome
-
Lossie AC, Whitney MM, Amidon D, Dong HJ, Chen P, Theriaque D, et al. (2001): Distinct phenotypes distinguish the molecular classes of Angelman syndrome. J Med Genet 38:834-845. (Pubitemid 34014208)
-
(2001)
Journal of Medical Genetics
, vol.38
, Issue.12
, pp. 834-845
-
-
Lossie, A.C.1
Whitney, M.M.2
Amidon, D.3
Dong, H.J.4
Chen, P.5
Theriaque, D.6
Hutson, A.7
Nicholls, R.D.8
Zori, R.T.9
Williams, C.A.10
Driscoll, D.J.11
-
2
-
-
33644865491
-
Angelman syndrome 2005: Updated consensus for diagnostic criteria
-
DOI 10.1002/ajmg.a.31074
-
Williams CA, Beaudet AL, Clayton-Smith J, Knoll JH, Kyllerman M, Laan LA, et al. (2006): Angelman syndrome 2005: Updated consensus for diagnostic criteria. Am J Med Genet A 140:413-418. (Pubitemid 43376311)
-
(2006)
American Journal of Medical Genetics
, vol.140 A
, Issue.5
, pp. 413-418
-
-
Williams, C.A.1
Beaudet, A.L.2
Clayton-Smith, J.3
Knoll, J.H.4
Kyllerman, M.5
Laan, L.A.6
Magenis, R.E.7
Moncla, A.8
Schinzel, A.A.9
Summers, J.A.10
Wagstaff, J.11
-
3
-
-
0031012849
-
UBE3A/E6-AP mutations cause Angelman syndrome
-
Kishino T, Lalande M, Wagstaff J (1997): UBE3A/E6-AP mutations cause Angelman syndrome. Nat Genet 15:70 -73.
-
(1997)
Nat Genet
, vol.15
, pp. 70-73
-
-
Kishino, T.1
Lalande, M.2
Wagstaff, J.3
-
4
-
-
0024619007
-
Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion
-
Knoll JH, Nicholls RD, Magenis RE, Graham JM Jr, Lalande M, Latt SA (1989): Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion. Am J Med Genet 32:285-290.
-
(1989)
Am J Med Genet
, vol.32
, pp. 285-290
-
-
Knoll, J.H.1
Nicholls, R.D.2
Magenis, R.E.3
Graham Jr., J.M.4
Lalande, M.5
Latt, S.A.6
-
5
-
-
0031031570
-
De novo truncating mutations in E6-Ap ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome
-
DOI 10.1038/ng0197-74
-
Matsuura T, Sutcliffe JS, Fang P, Galjaard RJ, Jiang YH, Benton CS, et al. (1997): De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome. Nat Genet 15:74-77. (Pubitemid 27014953)
-
(1997)
Nature Genetics
, vol.15
, Issue.1
, pp. 74-77
-
-
Matsuura, T.1
Sutcliffe, J.S.2
Fang, P.3
Galjaard, R.-J.4
Jiang, Y.-H.5
Benton, C.S.6
Rommens, J.M.7
Beaudet, A.L.8
-
6
-
-
0030890115
-
The E6-AP ubiquitin protein ligase (UBE3A) gene is localized within a narrowed Angelman syndrome critical region
-
Sutcliffe JS, Jiang YH, Galijaard RJ, Matsuura T, Fang P, Kubota T, et al. (1997): The E6-Ap ubiquitin-protein ligase (UBE3A) gene is localized within a narrowed Angelman syndrome critical region. Genome Res 7:368-377. (Pubitemid 27183005)
-
(1997)
Genome Research
, vol.7
, Issue.4
, pp. 368-377
-
-
Sutcliffe, J.S.1
Jiang, Y.-H.2
Galjaard, R.-J.3
Matsuura, T.4
Fang, P.5
Kubota, T.6
Christian, S.L.7
Bressler, J.8
Cattanach, B.9
Ledbetter, D.H.10
Beaudet, A.L.11
-
7
-
-
77954957575
-
Tissue-specific variation of Ube3a protein expression in rodents and in a mouse model of Angelman syndrome
-
Gustin RM, Bichell TJ, Bubser M, Daily J, Filonova I, Mrelashvili D, et al. (2010): Tissue-specific variation of Ube3a protein expression in rodents and in a mouse model of Angelman syndrome. Neurobiol Dis 39:283-291.
-
(2010)
Neurobiol Dis
, vol.39
, pp. 283-291
-
-
Gustin, R.M.1
Bichell, T.J.2
Bubser, M.3
Daily, J.4
Filonova, I.5
Mrelashvili, D.6
-
8
-
-
0030879482
-
Imprinted expression of the murine angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons
-
DOI 10.1038/ng0997-75
-
Albrecht U, Sutcliffe JS, Cattanach BM, Beechey CV, Armstrong D, Eichele G, Beaudet AL (1997): Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons. Nat Genet 17:75-78. (Pubitemid 27377535)
-
(1997)
Nature Genetics
, vol.17
, Issue.1
, pp. 75-78
-
-
Albrecht, U.1
Sutcliffe, J.S.2
Cattanach, B.M.3
Beechey, C.V.4
Armstrong, D.5
Eichele, G.6
Beaudet, A.L.7
-
9
-
-
0032103697
-
Imprinting in Angelman and Prader-Willi syndromes
-
DOI 10.1016/S0959-437X(98)80091-9
-
Jiang Y, Tsai TF, Bressler J, Beaudet AL (1998): Imprinting in Angelman and Prader-Willi syndromes. Curr Opin Genet Dev 8:334-342. (Pubitemid 28340086)
-
(1998)
Current Opinion in Genetics and Development
, vol.8
, Issue.3
, pp. 334-342
-
-
Jiang, Y.-H.1
Tsai, T.-F.2
Bressler, J.3
Beaudet, A.L.4
-
10
-
-
0032192481
-
Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation
-
DOI 10.1016/S0896-6273(00)80596-6
-
Jiang YH, Armstrong D, Albrecht U, Atkins CM, Noebels JL, Eichele G, et al. (1998): Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and longterm potentiation. Neuron 21:799-811. (Pubitemid 28498788)
-
(1998)
Neuron
, vol.21
, Issue.4
, pp. 799-811
-
-
Jiang, Y.-H.1
Armstrong, D.2
Albrecht, U.3
Atkins, C.M.4
Noebels, J.L.5
Eichele, G.6
Sweatt, J.D.7
Beaudet, A.L.8
-
11
-
-
33847210262
-
Rescue of neurological deficits in a mouse model for Angelman syndrome by reduction of alphaCaMKII inhibitory phosphorylation
-
van Woerden GM, Harris KD, Hojjati MR, Gustin RM, Qiu S, de Avila Freire R, et al. (2007): Rescue of neurological deficits in a mouse model for Angelman syndrome by reduction of alphaCaMKII inhibitory phosphorylation. Nat Neurosci 10:280 -282.
-
(2007)
Nat Neurosci
, vol.10
, pp. 280-282
-
-
Van Woerden, G.M.1
Harris, K.D.2
Hojjati, M.R.3
Gustin, R.M.4
Qiu, S.5
De Avila Freire, R.6
-
12
-
-
0026659262
-
Identification of heregulin, a specific activator of p185erbB2
-
Holmes WE, Sliwkowski MX, Akita RW, Henzel WJ, Lee J, Park JW, et al. (1992): Identification of heregulin, a specific activator of p185erbB2. Science 256:1205-1210.
-
(1992)
Science
, vol.256
, pp. 1205-1210
-
-
Holmes, W.E.1
Sliwkowski, M.X.2
Akita, R.W.3
Henzel, W.J.4
Lee, J.5
Park, J.W.6
-
13
-
-
0031059146
-
ARIA: A neuromuscular junction neuregulin
-
DOI 10.1146/annurev.neuro.20.1.429
-
Fischbach GD, Rosen KM (1997): ARIA: A neuromuscular junction neuregulin. Annu Rev Neurosci 20:429-458. (Pubitemid 27106389)
-
(1997)
Annual Review of Neuroscience
, vol.20
, pp. 429-458
-
-
Fischbach, G.D.1
Rosen, K.M.2
-
14
-
-
0033697710
-
Regulation of neuregulin signaling by PSD-95 interacting with ErbB4 at CNS synapses
-
Huang YZ, Won S, Ali DW, Wang Q, Tanowitz M, Du QS, et al. (2000): Regulation of neuregulin signaling by PSD-95 interacting with ErbB4 at CNS synapses. Neuron 26:443- 455.
-
(2000)
Neuron
, vol.26
, pp. 443-455
-
-
Huang, Y.Z.1
Won, S.2
Ali, D.W.3
Wang, Q.4
Tanowitz, M.5
Du, Q.S.6
-
15
-
-
26844565095
-
Neuregulin-1 reverses long-term potentiation at CA1 hippocampal synapses
-
DOI 10.1523/JNEUROSCI.2100-05.2005
-
Kwon OB, Longart M, Vullhorst D, Hoffman DA, Buonanno A (2005): Neuregulin-1 reverses long-term potentiation at CA1 hippocampal synapses. J Neurosci 25:9378-9383. (Pubitemid 41464750)
-
(2005)
Journal of Neuroscience
, vol.25
, Issue.41
, pp. 9378-9383
-
-
Kwon, O.-B.1
Longart, M.2
Vullhorst, D.3
Hoffman, D.A.4
Buonanno, A.5
-
16
-
-
38049158214
-
ErbB4 is a suppressor of long-term potentiation in the adult hippocampus
-
Pitcher GM, Beggs S, Woo RS, Mei L, Salter MW (2008): ErbB4 is a suppressor of long-term potentiation in the adult hippocampus. Neuroreport 19:139-143.
-
(2008)
Neuroreport
, vol.19
, pp. 139-143
-
-
Pitcher, G.M.1
Beggs, S.2
Woo, R.S.3
Mei, L.4
Salter, M.W.5
-
17
-
-
70049091165
-
Neuregulin 1 transgenic mice display reduced mismatch negativity, contextual fear conditioning and social interactions
-
Ehrlichman RS, Luminais SN, White SL, Rudnick ND, Ma N, Dow HC, et al. (2009): Neuregulin 1 transgenic mice display reduced mismatch negativity, contextual fear conditioning and social interactions. Brain Res 1294:116 -127.
-
(2009)
Brain Res
, vol.1294
, pp. 116-127
-
-
Ehrlichman, R.S.1
Luminais, S.N.2
White, S.L.3
Rudnick, N.D.4
Ma, N.5
Dow, H.C.6
-
18
-
-
33745912772
-
Altered neuregulin 1-erbB4 signaling contributes to NMDA receptor hypofunction in schizophrenia
-
DOI 10.1038/nm1418, PII NM1418
-
Hahn CG, Wang HY, Cho DS, Talbot K, Gur RE, Berrettini WH, et al. (2006): Altered neuregulin 1-erbB4 signaling contributes to NMDA receptor hypofunction in schizophrenia. Nat Med 12:824-828. (Pubitemid 44050073)
-
(2006)
Nature Medicine
, vol.12
, Issue.7
, pp. 824-828
-
-
Hahn, C.-G.1
Wang, H.-Y.2
Cho, D.-S.3
Talbot, K.4
Gur, R.E.5
Berrettini, W.H.6
Bakshi, K.7
Kamins, J.8
Borgmann-Winter, K.E.9
Siegel, S.J.10
Gallop, R.J.11
Arnold, S.E.12
-
19
-
-
43949084738
-
Neuregulin 1 in neural development, synaptic plasticity and schizophrenia
-
DOI 10.1038/nrn2392, PII NRN2392
-
Mei L, Xiong WC (2008): Neuregulin 1 in neural development, synaptic plasticity and schizophrenia. Nat Rev Neurosci 9:437-452. (Pubitemid 351704944)
-
(2008)
Nature Reviews Neuroscience
, vol.9
, Issue.6
, pp. 437-452
-
-
Mei, L.1
Xiong, W.-C.2
-
20
-
-
2542451853
-
Neuregulin 1-erbB signaling and the molecular/cellular basis of schizophrenia
-
DOI 10.1038/nn1258
-
Corfas G, Roy K, Buxbaum JD (2004): Neuregulin 1-erbB signaling and the molecular/cellular basis of schizophrenia. Nat Neurosci 7:575-580. (Pubitemid 38691892)
-
(2004)
Nature Neuroscience
, vol.7
, Issue.6
, pp. 575-580
-
-
Corfas, G.1
Roy, K.2
Buxbaum, J.D.3
-
21
-
-
0013375948
-
Neuregulin 1 and Susceptibility to Schizophrenia
-
Stefansson H, Sigurdsson E, Steinthorsdottir V, Bjornsdottir S, Sigmundsson T, Ghosh S, et al. (2002): Neuregulin 1 and susceptibility to schizophrenia. Am J Hum Genet 71:877-892. (Pubitemid 135750519)
-
(2002)
American Journal of Human Genetics
, vol.71
, Issue.4
, pp. 877-892
-
-
Stefansson, H.1
Sigurdsson, E.2
Steinthorsdottir, V.3
Bjornsdottir, S.4
Sigmundsson, T.5
Ghosh, S.6
Brynjolfsson, J.7
Gunnarsdottir, S.8
Ivarsson, O.9
Chou, T.T.10
Hjaltason, O.11
Birgisdottir, B.12
Jonsson, H.13
Gudnadottir, V.G.14
Gudmundsdottir, E.15
Bjornsson, A.16
Ingvarsson, B.17
Ingason, A.18
Sigfusson, S.19
Hardardottir, H.20
Harvey, R.P.21
Lai, D.22
Zhou, M.23
Brunner, D.24
Mutel, V.25
Gonzalo, A.26
Lemke, G.27
Sainz, J.28
Johannesson, G.29
Andresson, T.30
Gudbjartsson, D.31
Manolescu, A.32
Frigge, M.L.33
Gurney, M.E.34
Kong, A.35
Gulcher, J.R.36
Petursson, H.37
Stefansson, K.38
more..
-
22
-
-
46449111382
-
Genetic-linkage mapping of complex hereditary disorders to a whole-genome molecular-interaction network
-
DOI 10.1101/gr.075622.107
-
Iossifov I, Zheng T, Baron M, Gilliam TC, Rzhetsky A (2008): Geneticlinkage mapping of complex hereditary disorders to a whole-genome molecular-interaction network. Genome Res 18:1150-1162. (Pubitemid 351931166)
-
(2008)
Genome Research
, vol.18
, Issue.7
, pp. 1150-1162
-
-
Iossifov, I.1
Zheng, T.2
Baron, M.3
Gilliam, T.C.4
Rzhetsky, A.5
-
23
-
-
0037429649
-
Neuregulins: Functions, forms, and signaling strategies
-
Falls DL (2003): Neuregulins: Functions, forms, and signaling strategies. Exp Cell Res 284:14 -30.
-
(2003)
Exp Cell Res
, vol.284
, pp. 14-30
-
-
Falls, D.L.1
-
24
-
-
34248547353
-
Neuregulin-1 Enhances Depolarization-Induced GABA Release
-
DOI 10.1016/j.neuron.2007.04.009, PII S0896627307002590
-
Woo RS, Li XM, Tao Y, Carpenter-Hyland E, Huang YZ, Weber J, et al. (2007): Neuregulin-1 enhances depolarization-induced GABA release. Neuron 54:599-610. (Pubitemid 46756135)
-
(2007)
Neuron
, vol.54
, Issue.4
, pp. 599-610
-
-
Woo, R.-S.1
Li, X.-M.2
Tao, Y.3
Carpenter-Hyland, E.4
Huang, Y.Z.5
Weber, J.6
Neiswender, H.7
Dong, X.-P.8
Wu, J.9
Gassmann, M.10
Lai, C.11
Xiong, W.-C.12
Gao, T.-M.13
Mei, L.14
-
25
-
-
62649159446
-
Endocytosis and intracellular trafficking of ErbBs
-
Sorkin A, Goh LK (2009): Endocytosis and intracellular trafficking of ErbBs. Exp Cell Res 315:683- 696.
-
(2009)
Exp Cell Res
, vol.315
, pp. 683-696
-
-
Sorkin, A.1
Goh, L.K.2
-
26
-
-
41949128060
-
Isoform-specific monoubiquitination, endocytosis, and degradation of alternatively spliced ErbB4 isoforms
-
Sundvall M, Korhonen A, Paatero I, Gaudio E, Melino G, Croce CM, et al. (2008): Isoform-specific monoubiquitination, endocytosis, and degradation of alternatively spliced ErbB4 isoforms. Proc Natl Acad Sci U S A 105:4162- 4167.
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, pp. 4162-4167
-
-
Sundvall, M.1
Korhonen, A.2
Paatero, I.3
Gaudio, E.4
Melino, G.5
Croce, C.M.6
-
27
-
-
37549057995
-
The Angelman syndrome ubiquitin ligase localizes to the synapse and nucleus, and maternal deficiency results in abnormal dendritic spine morphology
-
Dindot SV, Antalffy BA, Bhattacharjee MB, Beaudet AL (2007): The Angelman syndrome ubiquitin ligase localizes to the synapse and nucleus, and maternal deficiency results in abnormal dendritic spine morphology. Hum Mol Genet 17:111-118.
-
(2007)
Hum Mol Genet
, vol.17
, pp. 111-118
-
-
Dindot, S.V.1
Antalffy, B.A.2
Bhattacharjee, M.B.3
Beaudet, A.L.4
-
28
-
-
19044365206
-
Regulation of NMDA receptors by neuregulin signaling in prefrontal cortex
-
DOI 10.1523/JNEUROSCI.1086-05.2005
-
Gu Z, Jiang Q, Fu AK, Ip NY, Yan Z (2005): Regulation of NMDA receptors by neuregulin signaling in prefrontal cortex. J Neurosci 25:4974-4984. (Pubitemid 40712840)
-
(2005)
Journal of Neuroscience
, vol.25
, Issue.20
, pp. 4974-4984
-
-
Gu, Z.1
Jiang, Q.2
Fu, A.K.Y.3
Ip, N.Y.4
Yan, Z.5
-
29
-
-
0037423916
-
Phosphorylation of the AMPA receptor GluR1 subunit is required for synaptic plasticity and retention of spatial memory
-
DOI 10.1016/S0092-8674(03)00122-3
-
Lee HK, Takamiya K, Han JS, Man H, Kim CH, Rumbaugh G, et al. (2003): Phosphorylation of the AMPA receptor GluR1 subunit is required for synaptic plasticity and retention of spatial memory. Cell 112:631-643. (Pubitemid 36331776)
-
(2003)
Cell
, vol.112
, Issue.5
, pp. 631-643
-
-
Lee, H.-K.1
Takamiya, K.2
Han, J.-S.3
Man, H.4
Kim, C.-H.5
Rumbaugh, G.6
Yu, S.7
Ding, L.8
He, C.9
Petralia, R.S.10
Wenthold, R.J.11
Gallagher, M.12
Huganir, R.L.13
-
30
-
-
34247543117
-
+/- knock-outs compared with wild-type mice
-
DOI 10.1523/JNEUROSCI.4314-06.2007
-
Bjarnadottir M, Misner DL, Haverfield-Gross S, Bruun S, Helgason VG, Stefansson H, et al. (2007): Neuregulin1 (NRG1) signaling through Fyn modulates NMDA receptor phosphorylation: Differential synaptic function in NRG1+/- knock-outs compared with wild-type mice. J Neurosci 27:4519-4529. (Pubitemid 46663586)
-
(2007)
Journal of Neuroscience
, vol.27
, Issue.17
, pp. 4519-4529
-
-
Bjarnadottir, M.1
Misner, D.L.2
Haverfield-Gross, S.3
Bruun, S.4
Helgason, V.G.5
Stefansson, H.6
Sigmundsson, A.7
Firth, D.R.8
Nielsen, B.9
Stefansdottir, R.10
Novak, T.J.11
Stefansson, K.12
Gurney, M.E.13
Andresson, T.14
-
31
-
-
49449092035
-
System-wide investigation of ErbB4 reveals 19 sites of Tyr phosphorylation that are unusually selective in their recruitment properties
-
Kaushansky A, Gordus A, Budnik BA, Lane WS, Rush J, MacBeath G (2008): System-wide investigation of ErbB4 reveals 19 sites of Tyr phosphorylation that are unusually selective in their recruitment properties. Chem Biol 15:808-817.
-
(2008)
Chem Biol
, vol.15
, pp. 808-817
-
-
Kaushansky, A.1
Gordus, A.2
Budnik, B.A.3
Lane, W.S.4
Rush, J.5
MacBeath, G.6
-
32
-
-
0030827595
-
Role of GGF/neuregulin signaling in interactions between migrating neurons and radial glia in the developing cerebral cortex
-
Anton ES, Marchionni MA, Lee KF, Rakic P (1997): Role of GGF/neuregulin signaling in interactions between migrating neurons and radial glia in the developing cerebral cortex. Development 124:3501-3510. (Pubitemid 27470034)
-
(1997)
Development
, vol.124
, Issue.18
, pp. 3501-3510
-
-
Anton, E.S.1
Marchionni, M.A.2
Lee, K.-F.3
Rakic, P.4
-
33
-
-
34249097991
-
Loss of erbB signaling in oligodendrocytes alters myelin and dopaminergic function, a potential mechanism for neuropsychiatric disorders
-
DOI 10.1073/pnas.0702157104
-
Roy K, Murtie JC, El-Khodor BF, Edgar N, Sardi SP, Hooks BM, et al. (2007): Loss of erbB signaling in oligodendrocytes alters myelin and dopaminergic function, a potential mechanism for neuropsychiatric disorders. Proc Natl Acad Sci U S A 104:8131-8136. (Pubitemid 47185887)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.19
, pp. 8131-8136
-
-
Roy, K.1
Murtie, J.C.2
El-Khodor, B.F.3
Edgar, N.4
Sardi, S.P.5
Hooks, B.M.6
Benoit-Marand, M.7
Chen, C.8
Moore, H.9
O'Donnell, P.10
Brunner, D.11
Corfas, G.12
-
34
-
-
0035938429
-
ErbB transmembrane tyrosine kinase receptors are differentially expressed throughout the adult rat central nervous system
-
Gerecke KM, Wyss JM, Karavanova I, Buonanno A, Carroll SL (2001): ErbB transmembrane tyrosine kinase receptors are differentially expressed throughout the adult rat central nervous system. J Comp Neurol 433:86-100.
-
(2001)
J Comp Neurol
, vol.433
, pp. 86-100
-
-
Gerecke, K.M.1
Wyss, J.M.2
Karavanova, I.3
Buonanno, A.4
Carroll, S.L.5
-
35
-
-
78649393990
-
Antipsychotic potential of quinazoline ErbB1 inhibitors in a schizophrenia model established with neonatal hippocampal lesioning
-
Mizuno M, Iwakura Y, Shibuya M, Zheng Y, Eda T, Kato T, et al. (2010): Antipsychotic potential of quinazoline ErbB1 inhibitors in a schizophrenia model established with neonatal hippocampal lesioning. J Pharmacol Sci 114:320 -331.
-
(2010)
J Pharmacol Sci
, vol.114
, pp. 320-331
-
-
Mizuno, M.1
Iwakura, Y.2
Shibuya, M.3
Zheng, Y.4
Eda, T.5
Kato, T.6
-
36
-
-
0035836642
-
Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia
-
DOI 10.1073/pnas.081071198
-
Hakak Y, Walker JR, Li C, Wong WH, Davis KL, Buxbaum JD, et al. (2001): Genome-wide expression analysis reveals dysregulation of myelination- related genes in chronic schizophrenia. Proc Natl Acad Sci U S A 98:4746-4751. (Pubitemid 32295047)
-
(2001)
Proceedings of the National Academy of Sciences of the United States of America
, vol.98
, Issue.8
, pp. 4746-4751
-
-
Hakak, Y.1
Walker, J.R.2
Li, C.3
Wong, W.H.4
Davis, K.L.5
Buxbaum, J.D.6
Haroutunian, V.7
Fienberg, A.A.8
-
37
-
-
0345701252
-
Derangements of hippocampal calcium/calmodulin-dependent protein kinase II in a mouse model for Angelman mental retardation syndrome
-
Weeber EJ, Jiang YH, Elgersma Y, Varga AW, Carrasquillo Y, Brown SE, et al. (2003): Derangements of hippocampal calcium/calmodulin-dependent protein kinase II in a mouse model for Angelman mental retardation syndrome. J Neurosci 23:2634-2644. (Pubitemid 36418598)
-
(2003)
Journal of Neuroscience
, vol.23
, Issue.7
, pp. 2634-2644
-
-
Weeber, E.J.1
Jiang, Y.-H.2
Elgersma, Y.3
Varga, A.W.4
Carrasquillo, Y.5
Brown, S.E.6
Christian, J.M.7
Mirnikjoo, B.8
Silva, A.9
Beaudet, A.L.10
Sweatt, J.D.11
-
38
-
-
78650756926
-
ErbB4 in parvalbumin-positive interneurons is critical for neuregulin 1 regulation of long-term potentiation
-
Chen YJ, Zhang M, Yin DM, Wen L, Ting A, Wang P, et al. (2010): ErbB4 in parvalbumin-positive interneurons is critical for neuregulin 1 regulation of long-term potentiation. Proc Natl Acad Sci U S A 107:21818-21823.
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, pp. 21818-21823
-
-
Chen, Y.J.1
Zhang, M.2
Yin, D.M.3
Wen, L.4
Ting, A.5
Wang, P.6
-
39
-
-
49149088555
-
Reversal of learning deficits in a Tsc2+/- Mouse model of tuberous sclerosis
-
Ehninger D, Han S, Shilyansky C, Zhou Y, Li W, Kwiatkowski DJ, et al. (2008): Reversal of learning deficits in a Tsc2+/- mouse model of tuberous sclerosis. Nat Med 14:843- 848.
-
(2008)
Nat Med
, vol.14
, pp. 843-848
-
-
Ehninger, D.1
Han, S.2
Shilyansky, C.3
Zhou, Y.4
Li, W.5
Kwiatkowski, D.J.6
-
40
-
-
75749114797
-
MTOR signaling: At the crossroads of plasticity, memory and disease
-
Hoeffer CA, Klann E (2010): mTOR signaling: At the crossroads of plasticity, memory and disease. Trends Neurosci 33:67-75.
-
(2010)
Trends Neurosci
, vol.33
, pp. 67-75
-
-
Hoeffer, C.A.1
Klann, E.2
-
41
-
-
44649116437
-
Systemic inhibition of mammalian target of rapamycin inhibits fear memory reconsolidation
-
Blundell J, Kouser M, Powell CM (2008): Systemic inhibition of mammalian target of rapamycin inhibits fear memory reconsolidation. Neurobiol Learn Mem 90:28-35.
-
(2008)
Neurobiol Learn Mem
, vol.90
, pp. 28-35
-
-
Blundell, J.1
Kouser, M.2
Powell, C.M.3
-
42
-
-
79955479386
-
Consolidation and reconsolidation of contextual fear memory requires mammalian target of rapamycin-dependent translation in the dorsal hippocampus
-
Gafford GM, Parsons RG, Helmstetter FJ (2011): Consolidation and reconsolidation of contextual fear memory requires mammalian target of rapamycin-dependent translation in the dorsal hippocampus. Neuroscience 182:98-104.
-
(2011)
Neuroscience
, vol.182
, pp. 98-104
-
-
Gafford, G.M.1
Parsons, R.G.2
Helmstetter, F.J.3
-
43
-
-
57749099197
-
ErbB4-neuregulin signaling modulates synapse development and dendritic arborization through distinct mechanisms
-
Krivosheya D, Tapia L, Levinson JN, Huang K, Kang Y, Hines R, et al. (2008): ErbB4-neuregulin signaling modulates synapse development and dendritic arborization through distinct mechanisms. J Biol Chem 283:32944-32956.
-
(2008)
J Biol Chem
, vol.283
, pp. 32944-32956
-
-
Krivosheya, D.1
Tapia, L.2
Levinson, J.N.3
Huang, K.4
Kang, Y.5
Hines, R.6
-
44
-
-
75749110218
-
Neuregulin 1 regulates pyramidal neuron activity via ErbB4 in parvalbumin-positive interneurons
-
Wen L, Lu YS, Zhu XH, Li XM, Woo RS, Chen YJ, et al. (2010): Neuregulin 1 regulates pyramidal neuron activity via ErbB4 in parvalbumin-positive interneurons. Proc Natl Acad Sci U S A 107:1211-1216.
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, pp. 1211-1216
-
-
Wen, L.1
Lu, Y.S.2
Zhu, X.H.3
Li, X.M.4
Woo, R.S.5
Chen, Y.J.6
-
45
-
-
77953053247
-
Selective populations of hippocampal interneurons express ErbB4 and their number and distribution is altered in ErbB4 knockout mice
-
Neddens J, Buonanno A (2010): Selective populations of hippocampal interneurons express ErbB4 and their number and distribution is altered in ErbB4 knockout mice. Hippocampus 20:724-744.
-
(2010)
Hippocampus
, vol.20
, pp. 724-744
-
-
Neddens, J.1
Buonanno, A.2
-
46
-
-
70349613442
-
Selective expression of ErbB4 in interneurons, but not pyramidal cells, of the rodent hippocampus
-
Vullhorst D, Neddens J, Karavanova I, Tricoire L, Petralia RS, McBain CJ, Buonanno A (2009): Selective expression of ErbB4 in interneurons, but not pyramidal cells, of the rodent hippocampus. J Neurosci 29:12255-12264.
-
(2009)
J Neurosci
, vol.29
, pp. 12255-12264
-
-
Vullhorst, D.1
Neddens, J.2
Karavanova, I.3
Tricoire, L.4
Petralia, R.S.5
McBain, C.J.6
Buonanno, A.7
-
47
-
-
12744253284
-
Angelman syndrome: Is there a characteristic EEG?
-
Laan LA, Vein AA (2005): Angelman syndrome: Is there a characteristic EEG? Brain Dev 27:80-87.
-
(2005)
Brain Dev
, vol.27
, pp. 80-87
-
-
Laan, L.A.1
Vein, A.A.2
-
49
-
-
0037328861
-
Angelman syndrome: A review of the clinical and genetic aspects
-
Clayton-Smith J, Laan L (2003): Angelman syndrome: A review of the clinical and genetic aspects. J Med Genet 40:87-95. (Pubitemid 36232812)
-
(2003)
Journal of Medical Genetics
, vol.40
, Issue.2
, pp. 87-95
-
-
Clayton-Smith, J.1
Laan, L.2
-
50
-
-
0042357395
-
The biology of epilepsy genes
-
Noebels JL (2003): The biology of epilepsy genes. Annu Rev Neurosci 26:599-625.
-
(2003)
Annu Rev Neurosci
, vol.26
, pp. 599-625
-
-
Noebels, J.L.1
-
51
-
-
0036371831
-
Channelopathies can cause epilepsy in man
-
Steinlein OK (2002): Channelopathies can cause epilepsy in man. Eur J Pain 6(suppl A):27-34.
-
(2002)
Eur J Pain
, vol.6
, Issue.SUPPL. A
, pp. 27-34
-
-
Steinlein, O.K.1
-
52
-
-
77955090532
-
Nicotinic receptor channelopathies and epilepsy
-
Steinlein OK, BertrandD(2010): Nicotinic receptor channelopathies and epilepsy. Pflugers Arch 460:495-503.
-
(2010)
Pflugers Arch
, vol.460
, pp. 495-503
-
-
Steinlein, O.K.1
Bertrand, D.2
-
53
-
-
28444458543
-
Differential expression of gamma-aminobutyric acid-A receptor subunits in rat dorsal and ventral hippocampus
-
DOI 10.1002/jnr.20670
-
Sotiriou E, Papatheodoropoulos C, Angelatou F (2005): Differential expression of gamma-aminobutyric acid-a receptor subunits in rat dorsal and ventral hippocampus. J Neurosci Res 82:690-700. (Pubitemid 41740469)
-
(2005)
Journal of Neuroscience Research
, vol.82
, Issue.5
, pp. 690-700
-
-
Sotiriou, E.1
Papatheodoropoulos, C.2
Angelatou, F.3
-
54
-
-
72749102220
-
Altered GABAA, slow inhibition and network oscillations in mice lacking the GABAA receptor beta3 subunit
-
Hentschke H, Benkwitz C, Banks MI, Perkins MG, Homanics GE, Pearce RA (2009): Altered GABAA, slow inhibition and network oscillations in mice lacking the GABAA receptor beta3 subunit. J Neurophysiol 102:3643-3655.
-
(2009)
J Neurophysiol
, vol.102
, pp. 3643-3655
-
-
Hentschke, H.1
Benkwitz, C.2
Banks, M.I.3
Perkins, M.G.4
Homanics, G.E.5
Pearce, R.A.6
-
55
-
-
70350349099
-
Angelman syndrome: Current understanding and research prospects
-
Dan B (2009): Angelman syndrome: Current understanding and research prospects. Epilepsia 50:2331-2339.
-
(2009)
Epilepsia
, vol.50
, pp. 2331-2339
-
-
Dan, B.1
-
56
-
-
33947673494
-
Pharmacotherapy for cognitive impairment in a mouse model of Down syndrome
-
DOI 10.1038/nn1860, PII NN1860
-
Fernandez F, Morishita W, Zuniga E, Nguyen J, Blank M, Malenka RC, Garner CC (2007): Pharmacotherapy for cognitive impairment in a mouse model of Down syndrome. Nat Neurosci 10:411-413. (Pubitemid 46494581)
-
(2007)
Nature Neuroscience
, vol.10
, Issue.4
, pp. 411-413
-
-
Fernandez, F.1
Morishita, W.2
Zuniga, E.3
Nguyen, J.4
Blank, M.5
Malenka, R.C.6
Garner, C.C.7
-
57
-
-
70450237623
-
A critical period in cortical interneuron neurogenesis in down syndrome revealed by human neural progenitor cells
-
Bhattacharyya A, McMillan E, Chen SI, Wallace K, Svendsen CN (2009): A critical period in cortical interneuron neurogenesis in down syndrome revealed by human neural progenitor cells. Dev Neurosci 31:497-510.
-
(2009)
Dev Neurosci
, vol.31
, pp. 497-510
-
-
Bhattacharyya, A.1
McMillan, E.2
Chen, S.I.3
Wallace, K.4
Svendsen, C.N.5
-
58
-
-
77952240568
-
Alteration of inhibitory circuits in the somatosensory cortex of Ts65Dn mice, a model for Down's syndrome
-
Perez-Cremades D, Hernandez S, Blasco-Ibanez JM, Crespo C, Nacher J, Varea E (2010): Alteration of inhibitory circuits in the somatosensory cortex of Ts65Dn mice, a model for Down's syndrome. J Neural Transm 117:445- 455.
-
(2010)
J Neural Transm
, vol.117
, pp. 445-455
-
-
Perez-Cremades, D.1
Hernandez, S.2
Blasco-Ibanez, J.M.3
Crespo, C.4
Nacher, J.5
Varea, E.6
-
59
-
-
42249107309
-
Mental retardation and associated neurological dysfunctions in Down syndrome: A consequence of dysregulation in critical chromosome 21 genes and associated molecular pathways
-
DOI 10.1016/j.ejpn.2007.08.010, PII S1090379807001535
-
Rachidi M, Lopes C (2008): Mental retardation and associated neurological dysfunctions in Down syndrome: A consequence of dysregulation in critical chromosome 21 genes and associated molecular pathways. Eur J Paediatr Neurol 12:168-182. (Pubitemid 351545848)
-
(2008)
European Journal of Paediatric Neurology
, vol.12
, Issue.3
, pp. 168-182
-
-
Rachidi, M.1
Lopes, C.2
-
60
-
-
77954851827
-
Defective GABAergic neurotransmission and pharmacological rescue of neuronal hyperexcitability in the amygdala in a mouse model of fragile X syndrome
-
Olmos-Serrano JL, Paluszkiewicz SM, Martin BS, Kaufmann WE, Corbin JG, Huntsman MM (2010): Defective GABAergic neurotransmission and pharmacological rescue of neuronal hyperexcitability in the amygdala in a mouse model of fragile X syndrome. J Neurosci 30:9929-9938.
-
(2010)
J Neurosci
, vol.30
, pp. 9929-9938
-
-
Olmos-Serrano, J.L.1
Paluszkiewicz, S.M.2
Martin, B.S.3
Kaufmann, W.E.4
Corbin, J.G.5
Huntsman, M.M.6
-
61
-
-
33846238191
-
Major defects in neocortical GABAergic inhibitory circuits in mice lacking the fragile X mental retardation protein
-
DOI 10.1016/j.neulet.2006.11.062, PII S030439400601202X
-
Selby L, Zhang C, SunQQ(2007): Major defects in neocortical GABAergic inhibitory circuits in mice lacking the fragile X mental retardation protein. Neurosci Lett 412:227-232. (Pubitemid 46109160)
-
(2007)
Neuroscience Letters
, vol.412
, Issue.3
, pp. 227-232
-
-
Selby, L.1
Zhang, C.2
Sun, Q.-Q.3
|