-
1
-
-
0026747761
-
Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA
-
Lewis JD, Meehan RR, Henzel WJ, et al. Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA. Cell 1992:69;905-14
-
(1992)
Cell
, vol.69
, pp. 905-914
-
-
Lewis, J.D.1
Meehan, R.R.2
Henzel, W.J.3
-
2
-
-
0027495467
-
Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2
-
Nan X, Meehan RR, Bird A. Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2. Nucleic Acids Res 1993:21;4886-92
-
(1993)
Nucleic Acids Res
, vol.21
, pp. 4886-4892
-
-
Nan, X.1
Meehan, R.R.2
Bird, A.3
-
3
-
-
0342437491
-
MeCP2 is a transcriptional represser with abundant binding sites in genomic chromatin
-
Nan X, Campoy FJ, Bird A. MeCP2 is a transcriptional represser with abundant binding sites in genomic chromatin. Cell 1997:88;471-81
-
(1997)
Cell
, vol.88
, pp. 471-481
-
-
Nan, X.1
Campoy, F.J.2
Bird, A.3
-
4
-
-
0036256510
-
Neuropathology and immunohistochemistry of brains with Rett syndrome
-
Itoh M, Takashima S. Neuropathology and immunohistochemistry of brains with Rett syndrome. No To Hattatsu 2002:34;211-16
-
(2002)
No To Hattatsu
, vol.34
, pp. 211-216
-
-
Itoh, M.1
Takashima, S.2
-
5
-
-
0242300623
-
Postnatal neurodevelopmental disorders: Meeting at the synapse?
-
Zoghbi Y. Postnatal neurodevelopmental disorders: Meeting at the synapse? Science: 2003:302;826-30
-
(2003)
Science
, vol.302
, pp. 826-830
-
-
Zoghbi, Y.1
-
6
-
-
0037081840
-
Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation
-
Shahbazian MD, Antalffy B, Armstrong DL, Zoghbi HY. Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation. Hum Mol Genet 2002;11:115-24
-
(2002)
Hum Mol Genet
, vol.11
, pp. 115-124
-
-
Shahbazian, M.D.1
Antalffy, B.2
Armstrong, D.L.3
Zoghbi, H.Y.4
-
7
-
-
0037381336
-
The expression of methyl CpG binding factor MeCP2 correlated with cellular differentiation in the developing rat brain and in cultured cells
-
Jung BP, Jugloff DGM, Zhang G, Logan R, Brown S, Eubanks JH. The expression of methyl CpG binding factor MeCP2 correlated with cellular differentiation in the developing rat brain and in cultured cells. J Neurobiol 2003:55;86-96
-
(2003)
J Neurobiol
, vol.55
, pp. 86-96
-
-
Jung, B.P.1
Jugloff, D.G.M.2
Zhang, G.3
Logan, R.4
Brown, S.5
Eubanks, J.H.6
-
8
-
-
0035870846
-
MECP2 is highly mutated in X-linked mental retardation
-
Couvert P, Bienvenu T, Aquaviva C, et al. MECP2 is highly mutated in X-linked mental retardation. Hum Mol Genet 2001:10;94l-46
-
(2001)
Hum Mol Genet
, vol.10
-
-
Couvert, P.1
Bienvenu, T.2
Aquaviva, C.3
-
9
-
-
18244432131
-
MECP2 mutation in male patients with non-specific X-linked mental retardation
-
Orrico A, Lam CW, Galli L, et al. MECP2 mutation in male patients with non-specific X-linked mental retardation. FEBS Lett 2000:481;285-88
-
(2000)
FEBS Lett
, vol.481
, pp. 285-288
-
-
Orrico, A.1
Lam, C.W.2
Galli, L.3
-
10
-
-
0035078664
-
ECP2 mutation in non-fatal, non-progressive encephalopathy in a male
-
Imessaoudene B, Bonnefont JP, Rover G, et al. ECP2 mutation in non-fatal, non-progressive encephalopathy in a male. J Med Genet 2001:38;171-74
-
(2001)
J Med Genet
, vol.38
, pp. 171-174
-
-
Imessaoudene, B.1
Bonnefont, J.P.2
Rover, G.3
-
13
-
-
0035094767
-
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome
-
Guy J, Hendrich B, Holmes M, Martin JE, Bird A. A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome. Nature Genet 2001:27;322-26
-
(2001)
Nature Genet
, vol.27
, pp. 322-326
-
-
Guy, J.1
Hendrich, B.2
Holmes, M.3
Martin, J.E.4
Bird, A.5
-
14
-
-
0035093830
-
Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
-
Chen RZ, Akbarian S, Tudor M, Jaenisch R. Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice. Nature Genet 2001:27;327-31
-
(2001)
Nature Genet
, vol.27
, pp. 327-331
-
-
Chen, R.Z.1
Akbarian, S.2
Tudor, M.3
Jaenisch, R.4
-
15
-
-
7244243971
-
MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decision
-
Kishi N, Macklis JD. MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decision. Mol Cell Neurosci 2004:27;306-21
-
(2004)
Mol Cell Neurosci
, vol.27
, pp. 306-321
-
-
Kishi, N.1
Macklis, J.D.2
-
17
-
-
0029059624
-
Pervasive neuroanatomic abnormalities of the brain in three cases of Rett's syndrome
-
Bauman ML, Kemper TL, Arin DM. Pervasive neuroanatomic abnormalities of the brain in three cases of Rett's syndrome. Neurology 1995:45;1581-86
-
(1995)
Neurology
, vol.45
, pp. 1581-1586
-
-
Bauman, M.L.1
Kemper, T.L.2
Arin, D.M.3
-
19
-
-
4444333589
-
The transcriptional repressor Mecp2 regulates terminal neuronal differentiation
-
Matarazzo V, Cohen D, Palmer AM, et al. The transcriptional repressor Mecp2 regulates terminal neuronal differentiation. Mol Cell Neurosci 2004;27:44-58
-
(2004)
Mol Cell Neurosci
, vol.27
, pp. 44-58
-
-
Matarazzo, V.1
Cohen, D.2
Palmer, A.M.3
-
21
-
-
0030071685
-
The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse
-
Tate P. Skames W, Bird A. The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse. Nat Genet 1996:12;205-8
-
(1996)
Nat Genet
, vol.12
, pp. 205-208
-
-
Tate, P.1
Skames, W.2
Bird, A.3
-
22
-
-
0037439239
-
Methyl-CpG-binding protein 2 is localized in the postsynaptic compartment: An immunochemical study of subcellular fractions
-
Aber KM, Non P, Macdonald SM, Bibat G, Jarrar MH, Kaufmann WE. Methyl-CpG-binding protein 2 is localized in the postsynaptic compartment: An immunochemical study of subcellular fractions. Neuroscience 2003:116;77-80
-
(2003)
Neuroscience
, vol.116
, pp. 77-80
-
-
Aber, K.M.1
Non, P.2
Macdonald, S.M.3
Bibat, G.4
Jarrar, M.H.5
Kaufmann, W.E.6
-
23
-
-
0027317286
-
Differential ontogenesis of presynaptic and postsynaptic GABAC inhibition in rat somatosensory cortex
-
Fukuda A, Mody I, Prince DA. Differential ontogenesis of presynaptic and postsynaptic GABAC inhibition in rat somatosensory cortex. J Neurophysiol 1993:70;448-52
-
(1993)
J Neurophysiol
, vol.70
, pp. 448-452
-
-
Fukuda, A.1
Mody, I.2
Prince, D.A.3
-
24
-
-
0043135219
-
Postnatal development and migration of cholecystokinin-immunoreactive interneurons in rat hippocampus
-
Morozov YM, Freund TF. Postnatal development and migration of cholecystokinin-immunoreactive interneurons in rat hippocampus. Neuroscience 2003:120;923-39
-
(2003)
Neuroscience
, vol.120
, pp. 923-939
-
-
Morozov, Y.M.1
Freund, T.F.2
-
25
-
-
0242624585
-
Neurotrophic factors in the pathogenesis of Rett syndrome
-
Riikonen R. Neurotrophic factors in the pathogenesis of Rett syndrome. J Child Neurol 2003;18:693-97
-
(2003)
J Child Neurol
, vol.18
, pp. 693-697
-
-
Riikonen, R.1
-
26
-
-
0242332183
-
Derepression of BDNF transcription involves calcium-dependent phosphorylation of MeCP2
-
Chen WG, Chang Q, Lin Y, et al. Derepression of BDNF transcription involves calcium-dependent phosphorylation of MeCP2. Science 2003:302;885-89
-
(2003)
Science
, vol.302
, pp. 885-889
-
-
Chen, W.G.1
Chang, Q.2
Lin, Y.3
-
27
-
-
0242300612
-
DNA methylation-related chromatin remodeling in activity-dependent BDNF gene regulation
-
Martinowich K, Hattori D, Wu H, et al. DNA methylation-related chromatin remodeling in activity-dependent BDNF gene regulation. Science 2003:302;890-93
-
(2003)
Science
, vol.302
, pp. 890-893
-
-
Martinowich, K.1
Hattori, D.2
Wu, H.3
-
28
-
-
0037063706
-
BDNF overexpression increases dendrite complexity in hippocampal dentate gyrus
-
Tolwani RJ, Buckmaster PS, Varma S, et al. BDNF overexpression increases dendrite complexity in hippocampal dentate gyrus. Neuroscience 2002:114;795-805
-
(2002)
Neuroscience
, vol.114
, pp. 795-805
-
-
Tolwani, R.J.1
Buckmaster, P.S.2
Varma, S.3
-
29
-
-
0035341088
-
Absence of hippocampal mossy fiber sprouting in transgenic mice overexpressing brain-derived neurotrophic factor
-
Qiao X, Suri C, Knusel B, Noebels JL. Absence of hippocampal mossy fiber sprouting in transgenic mice overexpressing brain-derived neurotrophic factor. J Neurosci Res 2001:64;268-76
-
(2001)
J Neurosci Res
, vol.64
, pp. 268-276
-
-
Qiao, X.1
Suri, C.2
Knusel, B.3
Noebels, J.L.4
-
30
-
-
0033797735
-
Dendritic anomalies in disorders associated with mental retardation
-
Kaufmann WE, Moser H. Dendritic anomalies in disorders associated with mental retardation. Cereb Cortex 2000:10;981-91
-
(2000)
Cereb Cortex
, vol.10
, pp. 981-991
-
-
Kaufmann, W.E.1
Moser, H.2
-
32
-
-
0037439744
-
Associative memory formation increases the observation of dendritic spines in the hippocampus
-
Leuner B, Falduto J, Shors T. Associative memory formation increases the observation of dendritic spines in the hippocampus. J Neurosci 2003:23;659-65
-
(2003)
J Neurosci
, vol.23
, pp. 659-665
-
-
Leuner, B.1
Falduto, J.2
Shors, T.3
-
33
-
-
0030744335
-
Rett syndrome: A disorder affecting early brain growth
-
Naidu S. Rett syndrome: A disorder affecting early brain growth. Ann Neurol 1997:42;3-10
-
(1997)
Ann Neurol
, vol.42
, pp. 3-10
-
-
Naidu, S.1
-
34
-
-
0027308186
-
Neiiroanatomy of Rett syndrome: A volumetric imaging study
-
Reiss AL, Faruque F, Naidu S, et al. Neiiroanatomy of Rett syndrome: A volumetric imaging study. Ann Neurol 1993:34;227-34
-
(1993)
Ann Neurol
, vol.34
, pp. 227-234
-
-
Reiss, A.L.1
Faruque, F.2
Naidu, S.3
-
35
-
-
0031028124
-
Neuroanatomy in Rett syndrome: Cerebral cortex and posterior fossa
-
Subramaniam B, Naidu S, Reiss AL. Neuroanatomy in Rett syndrome: Cerebral cortex and posterior fossa. Neurology 1997:48;399-407
-
(1997)
Neurology
, vol.48
, pp. 399-407
-
-
Subramaniam, B.1
Naidu, S.2
Reiss, A.L.3
-
36
-
-
0031761177
-
Decreased dendritic branching in frontal, motor and limbic cortex in Rett syndrome compared with Trisomy 21
-
Armstrong DD, Dunn K, Antalffyy B. Decreased dendritic branching in frontal, motor and limbic cortex in Rett syndrome compared with Trisomy 21. J Neuropathol Exp Neurol 1998:57;1013-17
-
(1998)
J Neuropathol Exp Neurol
, vol.57
, pp. 1013-1017
-
-
Armstrong, D.D.1
Dunn, K.2
Antalffyy, B.3
|