-
1
-
-
33744831161
-
Structure of the '30 nm' chromatin fibre: a key role for the linker histone
-
Robinson PJ, Rhodes D. Structure of the '30 nm' chromatin fibre: a key role for the linker histone. Curr Opin Struct Biol. 2006; 16: 336-43.
-
(2006)
Curr Opin Struct Biol.
, vol.16
, pp. 336-343
-
-
Robinson, P.J.1
Rhodes, D.2
-
2
-
-
17644391390
-
Linker histone variants control chromatin dynamics during early embryogenesis
-
Saeki H, Ohsumi K, Aihara H, Ito T, Hirose S, Ura K, Kaneda Y. Linker histone variants control chromatin dynamics during early embryogenesis. Proc Natl Acad Sci USA. 2005; 102: 5697-702.
-
(2005)
Proc Natl Acad Sci USA.
, vol.102
, pp. 5697-5702
-
-
Saeki, H.1
Ohsumi, K.2
Aihara, H.3
Ito, T.4
Hirose, S.5
Ura, K.6
Kaneda, Y.7
-
3
-
-
23444453570
-
Whole-genome views of chromatin structure
-
Loden M, van Steensel B. Whole-genome views of chromatin structure. Chromosome Res. 2005; 13: 289-98.
-
(2005)
Chromosome Res.
, vol.13
, pp. 289-298
-
-
Loden, M.1
van Steensel, B.2
-
4
-
-
8844265508
-
Epigenetic regulation of cellular memory by the Polycomb and Trithorax group proteins
-
Ringrose L, Paro R. Epigenetic regulation of cellular memory by the Polycomb and Trithorax group proteins. Annu Rev Genet. 2004; 38: 413-43.
-
(2004)
Annu Rev Genet.
, vol.38
, pp. 413-443
-
-
Ringrose, L.1
Paro, R.2
-
5
-
-
32344450824
-
Genomic DNA methylation: the mark and its mediators
-
Klose RJ, Bird AP. Genomic DNA methylation: the mark and its mediators. Trends Biochem Sci. 2006; 31: 89-97.
-
(2006)
Trends Biochem Sci.
, vol.31
, pp. 89-97
-
-
Klose, R.J.1
Bird, A.P.2
-
6
-
-
0032574977
-
Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex
-
Nan X, Ng HH, Johnson CA, Laherty CD, Turner BM, Eisenman RN, Bird A. Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex. Nature 1998; 393: 386-9.
-
(1998)
Nature
, vol.393
, pp. 386-389
-
-
Nan, X.1
Ng, H.H.2
Johnson, C.A.3
Laherty, C.D.4
Turner, B.M.5
Eisenman, R.N.6
Bird, A.7
-
7
-
-
0036322622
-
Genetic analyses of DNA methyltransferase genes in mouse model system
-
Okano M, Li E. Genetic analyses of DNA methyltransferase genes in mouse model system. J Nutr. 2002; 132: 2462S-5S.
-
(2002)
J Nutr.
, vol.132
-
-
Okano, M.1
Li, E.2
-
8
-
-
0032102949
-
Dnmt2 is not required for de novo and maintenance methylation of viral DNA in embryonic stem cells
-
Okano M, Xie S, Li E. Dnmt2 is not required for de novo and maintenance methylation of viral DNA in embryonic stem cells. Nucleic Acids Res. 1998; 26: 2536-40.
-
(1998)
Nucleic Acids Res.
, vol.26
, pp. 2536-2540
-
-
Okano, M.1
Xie, S.2
Li, E.3
-
9
-
-
29244449333
-
Histone H1 depletion in mammals alters global chromatin structure but causes specific changes in gene regulation
-
Fan Y, Nikitina T, Zhao J, Fleury TJ, Bhattacharyya R, Bouhassira EE, Stein A, Woodcock CL, Skoultchi AI. Histone H1 depletion in mammals alters global chromatin structure but causes specific changes in gene regulation. Cell 2005; 123: 1199-212.
-
(2005)
Cell
, vol.123
, pp. 1199-1212
-
-
Fan, Y.1
Nikitina, T.2
Zhao, J.3
Fleury, T.J.4
Bhattacharyya, R.5
Bouhassira, E.E.6
Stein, A.7
Woodcock, C.L.8
Skoultchi, A.I.9
-
10
-
-
29244454263
-
Gene regulation by histone H1: new links to DNA methylation
-
Rupp RA, Becker PB. Gene regulation by histone H1: new links to DNA methylation. Cell 2005; 123: 1178-9.
-
(2005)
Cell
, vol.123
, pp. 1178-1179
-
-
Rupp, R.A.1
Becker, P.B.2
-
11
-
-
22844457491
-
DNA methylation and human disease
-
Robertson KD. DNA methylation and human disease. Nat Rev Genet. 2005; 6: 597-610.
-
(2005)
Nat Rev Genet.
, vol.6
, pp. 597-610
-
-
Robertson, K.D.1
-
12
-
-
16544395591
-
DNA methylation and cancer
-
Das PM, Singal R. DNA methylation and cancer. J Clin Oncol. 2004; 22: 4632-42.
-
(2004)
J Clin Oncol.
, vol.22
, pp. 4632-4642
-
-
Das, P.M.1
Singal, R.2
-
13
-
-
24744453331
-
Methyl-CpG-binding proteins in cancer: blaming the DNA methylation messenger
-
Ballestar E, Esteller M. Methyl-CpG-binding proteins in cancer: blaming the DNA methylation messenger. Biochem Cell Biol. 2005; 83: 374-84.
-
(2005)
Biochem Cell Biol.
, vol.83
, pp. 374-384
-
-
Ballestar, E.1
Esteller, M.2
-
14
-
-
2642531973
-
Epigenetics in human disease and prospects for epigenetic therapy
-
Egger G, Liang G, Aparicio A, Jones PA. Epigenetics in human disease and prospects for epigenetic therapy. Nature 2004; 429: 457-63.
-
(2004)
Nature
, vol.429
, pp. 457-463
-
-
Egger, G.1
Liang, G.2
Aparicio, A.3
Jones, P.A.4
-
15
-
-
0035977865
-
Genomic imprinting and cancer; new paradigms in the genetics of neoplasia
-
Schofield PN, Joyce JA, Lam WK, Grandjean V, Ferguson-Smith A, Reik W, Maher ER. Genomic imprinting and cancer; new paradigms in the genetics of neoplasia. Toxicol Lett. 2001; 120: 151-60.
-
(2001)
Toxicol Lett.
, vol.120
, pp. 151-160
-
-
Schofield, P.N.1
Joyce, J.A.2
Lam, W.K.3
Grandjean, V.4
Ferguson-Smith, A.5
Reik, W.6
Maher, E.R.7
-
17
-
-
24344466882
-
DNA methylation and histone modifications: teaming up to silence genes
-
Fuks F. DNA methylation and histone modifications: teaming up to silence genes. Curr Opin Genet Dev. 2005; 15: 490-5.
-
(2005)
Curr Opin Genet Dev.
, vol.15
, pp. 490-495
-
-
Fuks, F.1
-
19
-
-
23744457857
-
How epigenetics integrates nuclear functions. Workshop on epigenetics and chromatin: transcriptional regulation and beyond
-
Esteller M, Almouzni G. How epigenetics integrates nuclear functions. Workshop on epigenetics and chromatin: transcriptional regulation and beyond. EMBO Rep. 2005; 6: 624-8.
-
(2005)
EMBO Rep.
, vol.6
, pp. 624-628
-
-
Esteller, M.1
Almouzni, G.2
-
20
-
-
1042290351
-
The SWI/SNF complex-chro-matin and cancer
-
Roberts CW, Orkin SH. The SWI/SNF complex-chro-matin and cancer. Nat Rev Cancer 2004; 4: 133-42.
-
(2004)
Nat Rev Cancer
, vol.4
, pp. 133-142
-
-
Roberts, C.W.1
Orkin, S.H.2
-
21
-
-
0034610814
-
The language of covalent histone modifications
-
Strahl BD, Allis CD. The language of covalent histone modifications. Nature 2000; 403: 41-5.
-
(2000)
Nature
, vol.403
, pp. 41-45
-
-
Strahl, B.D.1
Allis, C.D.2
-
22
-
-
0035839136
-
Translating the histone code
-
Jenuwein T, Allis CD. Translating the histone code. Science 2001; 293: 1074-80.
-
(2001)
Science
, vol.293
, pp. 1074-1080
-
-
Jenuwein, T.1
Allis, C.D.2
-
23
-
-
0042671367
-
Cracking the histone code: one, two, three methyls, you're out!
-
Dutnall RN. Cracking the histone code: one, two, three methyls, you're out! Mol Cell. 2003; 12: 3-4.
-
(2003)
Mol Cell
, vol.12
, pp. 3-4
-
-
Dutnall, R.N.1
-
24
-
-
14144250266
-
Negative correlation between poly-ADP-ribosylation of spleen cell his-tone proteins and initial duration of dimethylnitrosamine exposure to mice in vivo measured by Western blot immunoprobe assay: a possible biomarker for cancer detection
-
Devi BJ, Schneeweiss FH, Sharan RN. Negative correlation between poly-ADP-ribosylation of spleen cell his-tone proteins and initial duration of dimethylnitrosamine exposure to mice in vivo measured by Western blot immunoprobe assay: a possible biomarker for cancer detection. Cancer Detect Prev. 2005; 29: 66-71.
-
(2005)
Cancer Detect Prev.
, vol.29
, pp. 66-71
-
-
Devi, B.J.1
Schneeweiss, F.H.2
Sharan, R.N.3
-
25
-
-
2942707810
-
Long-term memory requires polyADP-ribosylation
-
Cohen-Armon M, Visochek L, Katzoff A, Levitan D, Susswein AJ, Klein R, Valbrun M, Schwartz JH. Long-term memory requires polyADP-ribosylation. Science 2004; 304: 1820-2.
-
(2004)
Science
, vol.304
, pp. 1820-1822
-
-
Cohen-Armon, M.1
Visochek, L.2
Katzoff, A.3
Levitan, D.4
Susswein, A.J.5
Klein, R.6
Valbrun, M.7
Schwartz, J.H.8
-
26
-
-
23744506898
-
PolyADP-ribosylation is involved in neurotrophic activity
-
Visochek L, Steingart RA, Vulih-Shultzman I, Klein R, Priel E, Gozes I, Cohen-Armon M. PolyADP-ribosylation is involved in neurotrophic activity. J Neurosci. 2005; 25: 7420-8.
-
(2005)
J Neurosci.
, vol.25
, pp. 7420-7428
-
-
Visochek, L.1
Steingart, R.A.2
Vulih-Shultzman, I.3
Klein, R.4
Priel, E.5
Gozes, I.6
Cohen-Armon, M.7
-
27
-
-
0038682011
-
PARP goes transcription
-
Kraus WL, Lis JT. PARP goes transcription. Cell 2003; 113: 677-83.
-
(2003)
Cell
, vol.113
, pp. 677-683
-
-
Kraus, W.L.1
Lis, J.T.2
-
28
-
-
33744976344
-
Applying whole-genome studies of epigenetic regulation to study human disease
-
Lieb JD, Beck S, Bulyk ML, Farnham P, Hattori N, Henikoff S, Liu XS, Okumura K, Shiota K, Ushijima T, Greally JM. Applying whole-genome studies of epigenetic regulation to study human disease. Cytogenet Genome Res. 2006; 114: 1-15.
-
(2006)
Cytogenet Genome Res.
, vol.114
, pp. 1-15
-
-
Lieb, J.D.1
Beck, S.2
Bulyk, M.L.3
Farnham, P.4
Hattori, N.5
Henikoff, S.6
Liu, X.S.7
Okumura, K.8
Shiota, K.9
Ushijima, T.10
Greally, J.M.11
-
29
-
-
33644851120
-
Altered gene silencing and human diseases
-
Perini G, Tupler R. Altered gene silencing and human diseases. Clin Genet. 2006; 69: 1-7.
-
(2006)
Clin Genet.
, vol.69
, pp. 1-7
-
-
Perini, G.1
Tupler, R.2
-
30
-
-
32544431582
-
Epigenetics and human disease: translating basic biology into clinical applications
-
Rodenhiser D, Mann M. Epigenetics and human disease: translating basic biology into clinical applications. CMAJ. 2006; 174: 341-8.
-
(2006)
CMAJ.
, vol.174
, pp. 341-348
-
-
Rodenhiser, D.1
Mann, M.2
-
31
-
-
6044256118
-
Histones and histone modifications
-
Peterson CL, Laniel MA. Histones and histone modifications. Curr Biol. 2004; 14: R546-51.
-
(2004)
Curr Biol.
, vol.14
-
-
Peterson, C.L.1
Laniel, M.A.2
-
32
-
-
33744783407
-
Histone modification patterns associated with the human X chromosome
-
Brinkman AB, Roelofsen T, Pennings SW, Martens JH, Jenuwein T, Stunnenberg HG. Histone modification patterns associated with the human X chromosome. EMBO Rep. 2006; 7: 628-34.
-
(2006)
EMBO Rep.
, vol.7
, pp. 628-634
-
-
Brinkman, A.B.1
Roelofsen, T.2
Pennings, S.W.3
Martens, J.H.4
Jenuwein, T.5
Stunnenberg, H.G.6
-
33
-
-
11144332565
-
Histone demethylation mediated by the nuclear amine oxidase homolog LSD1
-
Shi Y, Lan F, Matson C, Mulligan P, Whetstine JR, Cole PA, Casero RA, Shi Y. Histone demethylation mediated by the nuclear amine oxidase homolog LSD1. Cell 2004; 119: 941-53.
-
(2004)
Cell
, vol.119
, pp. 941-953
-
-
Shi, Y.1
Lan, F.2
Matson, C.3
Mulligan, P.4
Whetstine, J.R.5
Cole, P.A.6
Casero, R.A.7
Shi, Y.8
-
34
-
-
32844454603
-
Histone demethylation by a family of JmjC domain-containing proteins
-
Tsukada Y, Fang J, Erdjument-Bromage H, Warren ME, Borchers CH, Tempst P, Zhang Y. Histone demethylation by a family of JmjC domain-containing proteins. Nature 2006; 439: 811-6.
-
(2006)
Nature
, vol.439
, pp. 811-816
-
-
Tsukada, Y.1
Fang, J.2
Erdjument-Bromage, H.3
Warren, M.E.4
Borchers, C.H.5
Tempst, P.6
Zhang, Y.7
-
35
-
-
33747455678
-
JmjC-domain-containing proteins and histone demethylation
-
Klose RJ, Kallin EM, Zhang Y. JmjC-domain-containing proteins and histone demethylation. Nat Rev Genet. 2006; 7: 715-27.
-
(2006)
Nat Rev Genet.
, vol.7
, pp. 715-727
-
-
Klose, R.J.1
Kallin, E.M.2
Zhang, Y.3
-
36
-
-
33746069681
-
Dosage compensation in mammals: fine-tuning the expression of the X chromosome
-
Heard E, Disteche CM. Dosage compensation in mammals: fine-tuning the expression of the X chromosome. Genes Dev. 2006; 20: 1848-67.
-
(2006)
Genes Dev.
, vol.20
, pp. 1848-1867
-
-
Heard, E.1
Disteche, C.M.2
-
37
-
-
27844503601
-
Evidence for de novo imprinted X-chromosome inactivation independent of meiotic inacti-vation in mice
-
Okamoto I, Arnaud D, Le Baccon P, Otte AP, Disteche CM, Avner P, Heard E. Evidence for de novo imprinted X-chromosome inactivation independent of meiotic inacti-vation in mice. Nature 2005; 438: 369-73.
-
(2005)
Nature
, vol.438
, pp. 369-373
-
-
Okamoto, I.1
Arnaud, D.2
Le Baccon, P.3
Otte, A.P.4
Disteche, C.M.5
Avner, P.6
Heard, E.7
-
38
-
-
33644557773
-
Transient homologous chromosome pairing marks the onset of X inactivation
-
Xu N, Tsai CL, Lee JT. Transient homologous chromosome pairing marks the onset of X inactivation. Science 2006; 311: 1149-52.
-
(2006)
Science
, vol.311
, pp. 1149-1152
-
-
Xu, N.1
Tsai, C.L.2
Lee, J.T.3
-
39
-
-
33644751726
-
Transient colocalization of X-inactivation centres accompanies the initiation of X inactivation
-
Bacher CP, Guggiari M, Brors B, Augui S, Clerc P, Avner P, Eils R, Heard E. Transient colocalization of X-inactivation centres accompanies the initiation of X inactivation. Nat Cell Biol. 2006; 8: 293-9.
-
(2006)
Nat Cell Biol.
, vol.8
, pp. 293-299
-
-
Bacher, C.P.1
Guggiari, M.2
Brors, B.3
Augui, S.4
Clerc, P.5
Avner, P.6
Eils, R.7
Heard, E.8
-
41
-
-
0025273145
-
Neuron-specific expression of the rat brain type II sodium channel gene is directed by upstream regulatory elements
-
Maue RA, Kraner SD, Goodman RH, Mandel G. Neuron-specific expression of the rat brain type II sodium channel gene is directed by upstream regulatory elements. Neuron 1990; 4: 223-31.
-
(1990)
Neuron
, vol.4
, pp. 223-231
-
-
Maue, R.A.1
Kraner, S.D.2
Goodman, R.H.3
Mandel, G.4
-
43
-
-
0033306577
-
Transcriptional repression by REST: recruitment of Sin3A and histone deacetylase to neuronal genes
-
Huang Y, Myers SJ, Dingledine R. Transcriptional repression by REST: recruitment of Sin3A and histone deacetylase to neuronal genes. Nat Neurosci. 1999; 2: 867-72.
-
(1999)
Nat Neurosci.
, vol.2
, pp. 867-872
-
-
Huang, Y.1
Myers, S.J.2
Dingledine, R.3
-
44
-
-
0033598827
-
Neural restrictive silencer factor recruits mSin3 and histone deacetylase complex to repress neuron-specific target genes
-
Naruse Y, Aoki T, Kojima T, Mori N. Neural restrictive silencer factor recruits mSin3 and histone deacetylase complex to repress neuron-specific target genes. Proc Natl Acad Sci USA. 1999; 96: 13691-6.
-
(1999)
Proc Natl Acad Sci USA.
, vol.96
, pp. 13691-13696
-
-
Naruse, Y.1
Aoki, T.2
Kojima, T.3
Mori, N.4
-
45
-
-
17944383136
-
Regulation of neuronal traits by a novel transcriptional complex
-
Ballas N, Battaglioli E, Atouf F, Andres ME, Chenoweth J, Anderson ME, Burger C, Moniwa M, Davie JR, Bowers WJ, Federoff HJ, Rose DW, Rosenfeld MG, Brehm P, Mandel G. Regulation of neuronal traits by a novel transcriptional complex. Neuron 2001; 31: 353-65.
-
(2001)
Neuron
, vol.31
, pp. 353-365
-
-
Ballas, N.1
Battaglioli, E.2
Atouf, F.3
Andres, M.E.4
Chenoweth, J.5
Anderson, M.E.6
Burger, C.7
Moniwa, M.8
Davie, J.R.9
Bowers, W.J.10
Federoff, H.J.11
Rose, D.W.12
Rosenfeld, M.G.13
Brehm, P.14
Mandel, G.15
-
46
-
-
0037175017
-
REST repression of neuronal genes requires components of the hSWI.SNF complex
-
Battaglioli E, Andres ME, Rose DW, Chenoweth JG, Rosenfeld MG, Anderson ME, Mandel G. REST repression of neuronal genes requires components of the hSWI.SNF complex. J Biol Chem. 2002; 277: 41038-45.
-
(2002)
J Biol Chem.
, vol.277
, pp. 41038-41045
-
-
Battaglioli, E.1
Andres, M.E.2
Rose, D.W.3
Chenoweth, J.G.4
Rosenfeld, M.G.5
Anderson, M.E.6
Mandel, G.7
-
47
-
-
25144519737
-
An essential role for CoREST in nucleosomal histone 3 lysine 4 demethylation
-
Lee MG, Wynder C, Cooch N, Shiekhattar R. An essential role for CoREST in nucleosomal histone 3 lysine 4 demethylation. Nature 2005; 437: 432-5.
-
(2005)
Nature
, vol.437
, pp. 432-435
-
-
Lee, M.G.1
Wynder, C.2
Cooch, N.3
Shiekhattar, R.4
-
48
-
-
19344378337
-
REST and its corepressors mediate plasticity of neuronal gene chromatin throughout neurogenesis
-
Ballas N, Grunseich C, Lu DD, Speh JC, Mandel G. REST and its corepressors mediate plasticity of neuronal gene chromatin throughout neurogenesis. Cell 2005; 121: 645-57.
-
(2005)
Cell
, vol.121
, pp. 645-657
-
-
Ballas, N.1
Grunseich, C.2
Lu, D.D.3
Speh, J.C.4
Mandel, G.5
-
49
-
-
25844518743
-
The many faces of REST oversee epigenetic programming of neuronal genes
-
Ballas N, Mandel G. The many faces of REST oversee epigenetic programming of neuronal genes. Curr Opin Neurobiol. 2005; 15: 500-6.
-
(2005)
Curr Opin Neurobiol.
, vol.15
, pp. 500-506
-
-
Ballas, N.1
Mandel, G.2
-
50
-
-
33748350491
-
A repressor complex, AP4 transcription factor and geminin, negatively regulates expression of target genes in nonneuronal cells
-
Kim MY, Jeong BC, Lee JH, Kee HJ, Kook H, Kim NS, Kim YH, Kim JK, Ahn KY, Kim KK. A repressor complex, AP4 transcription factor and geminin, negatively regulates expression of target genes in nonneuronal cells. Proc Natl Acad Sci USA. 2006; 103: 13074-9.
-
(2006)
Proc Natl Acad Sci USA.
, vol.103
, pp. 13074-13079
-
-
Kim, M.Y.1
Jeong, B.C.2
Lee, J.H.3
Kee, H.J.4
Kook, H.5
Kim, N.S.6
Kim, Y.H.7
Kim, J.K.8
Ahn, K.Y.9
Kim, K.K.10
-
51
-
-
33646228863
-
Chromatin remodeling and neuronal function: exciting links
-
Santos M, Coelho PA, Maciel P. Chromatin remodeling and neuronal function: exciting links. Genes Brain Behav. 2006; 5: 80-91.
-
(2006)
Genes Brain Behav.
, vol.5
, pp. 80-91
-
-
Santos, M.1
Coelho, P.A.2
Maciel, P.3
-
53
-
-
0035234557
-
Genomic imprinting: parental influence on the genome
-
Reik W, Walter J. Genomic imprinting: parental influence on the genome. Nat Rev Genet. 2001; 2: 21-32.
-
(2001)
Nat Rev Genet.
, vol.2
, pp. 21-32
-
-
Reik, W.1
Walter, J.2
-
55
-
-
0035777024
-
Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes
-
Nicholls RD, Knepper JL. Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes. Annu Rev Genomics Hum Genet. 2001; 2: 153-75.
-
(2001)
Annu Rev Genomics Hum Genet.
, vol.2
, pp. 153-175
-
-
Nicholls, R.D.1
Knepper, J.L.2
-
56
-
-
0037389185
-
Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development
-
Weksberg R, Smith AC, Squire J, Sadowski P. Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development. Hum Mol Genet. 2003; 12: R61-8.
-
(2003)
Hum Mol Genet.
, vol.12
-
-
Weksberg, R.1
Smith, A.C.2
Squire, J.3
Sadowski, P.4
-
57
-
-
26444490720
-
Imprinting centers, chromatin structure, and disease
-
Soejima H, Wagstaff J. Imprinting centers, chromatin structure, and disease. J Cell Biochem. 2005; 95: 226-33.
-
(2005)
J Cell Biochem.
, vol.95
, pp. 226-233
-
-
Soejima, H.1
Wagstaff, J.2
-
58
-
-
33645457011
-
Imprinting in neurons
-
Kishino T. Imprinting in neurons. Cytogenet Genome Res. 2006; 113: 209-14.
-
(2006)
Cytogenet Genome Res.
, vol.113
, pp. 209-214
-
-
Kishino, T.1
-
59
-
-
0033759439
-
Decrease in reelin and glutamic acid decarboxylase67 (GAD67) expression in schizophrenia and bipolar disorder: a postmortem brain study
-
Guidotti A, Auta J, Davis JM, Di-Giorgi-Gerevini V, Dwivedi Y, Grayson DR, Impagnatiello F, Pandey G, Pesold C, Sharma R, Uzunov D, Costa E. Decrease in reelin and glutamic acid decarboxylase67 (GAD67) expression in schizophrenia and bipolar disorder: a postmortem brain study. Arch Gen Psychiatry 2000; 57: 1061-9.
-
(2000)
Arch Gen Psychiatry
, vol.57
, pp. 1061-1069
-
-
Guidotti, A.1
Auta, J.2
Davis, J.M.3
Di-Giorgi-Gerevini, V.4
Dwivedi, Y.5
Grayson, D.R.6
Impagnatiello, F.7
Pandey, G.8
Pesold, C.9
Sharma, R.10
Uzunov, D.11
Costa, E.12
-
60
-
-
13044276244
-
A decrease of reelin expression as a putative vulnerability factor in schizophrenia
-
Impagnatiello F, Guidotti AR, Pesold C, Dwivedi Y, Caruncho H, Pisu MG, Uzunov DP, Smalheiser NR, Davis JM, Pandey GN, Pappas GD, Tueting P, Sharma RP, Costa E. A decrease of reelin expression as a putative vulnerability factor in schizophrenia. Proc Natl Acad Sci USA. 1998; 95: 15718-23.
-
(1998)
Proc Natl Acad Sci USA.
, vol.95
, pp. 15718-15723
-
-
Impagnatiello, F.1
Guidotti, A.R.2
Pesold, C.3
Dwivedi, Y.4
Caruncho, H.5
Pisu, M.G.6
Uzunov, D.P.7
Smalheiser, N.R.8
Davis, J.M.9
Pandey, G.N.10
Pappas, G.D.11
Tueting, P.12
Sharma, R.P.13
Costa, E.14
-
61
-
-
0037627336
-
A reelin-integrin receptor interaction regulates Arc mRNA translation in synaptoneurosomes
-
Dong E, Caruncho H, Liu WS, Smalheiser NR, Grayson DR, Costa E, Guidotti A. A reelin-integrin receptor interaction regulates Arc mRNA translation in synaptoneurosomes. Proc Natl Acad Sci USA. 2003; 100: 5479-84.
-
(2003)
Proc Natl Acad Sci USA.
, vol.100
, pp. 5479-5484
-
-
Dong, E.1
Caruncho, H.2
Liu, W.S.3
Smalheiser, N.R.4
Grayson, D.R.5
Costa, E.6
Guidotti, A.7
-
62
-
-
0347719319
-
DNA-methyltransferase 1 mRNA is selectively overexpressed in telen-cephalic GABAergic interneurons of schizophrenia brains
-
Veldic M, Caruncho HJ, Liu WS, Davis J, Satta R, Grayson DR, Guidotti A, Costa E. DNA-methyltransferase 1 mRNA is selectively overexpressed in telen-cephalic GABAergic interneurons of schizophrenia brains. Proc Natl Acad Sci USA. 2004; 101: 348-53.
-
(2004)
Proc Natl Acad Sci USA.
, vol.101
, pp. 348-353
-
-
Veldic, M.1
Caruncho, H.J.2
Liu, W.S.3
Davis, J.4
Satta, R.5
Grayson, D.R.6
Guidotti, A.7
Costa, E.8
-
63
-
-
0037168650
-
An epigenetic mouse model for molecular and behavioral neuropathologies related to schizophrenia vulnerability
-
Tremolizzo L, Carboni G, Ruzicka WB, Mitchell CP, Sugaya I, Tueting P, Sharma R, Grayson DR, Costa E, Guidotti A. An epigenetic mouse model for molecular and behavioral neuropathologies related to schizophrenia vulnerability. Proc Natl Acad Sci USA. 2002; 99: 17095-100.
-
(2002)
Proc Natl Acad Sci USA.
, vol.99
, pp. 17095-17100
-
-
Tremolizzo, L.1
Carboni, G.2
Ruzicka, W.B.3
Mitchell, C.P.4
Sugaya, I.5
Tueting, P.6
Sharma, R.7
Grayson, D.R.8
Costa, E.9
Guidotti, A.10
-
64
-
-
13444271572
-
DNA methyltransferase 1 regulates reelin mRNA expression in mouse primary cortical cultures
-
Noh JS, Sharma RP, Veldic M, Salvacion AA, Jia X, Chen Y, Costa E, Guidotti A, Grayson DR. DNA methyltransferase 1 regulates reelin mRNA expression in mouse primary cortical cultures. Proc Natl Acad Sci USA. 2005; 102: 1749-54.
-
(2005)
Proc Natl Acad Sci USA.
, vol.102
, pp. 1749-1754
-
-
Noh, J.S.1
Sharma, R.P.2
Veldic, M.3
Salvacion, A.A.4
Jia, X.5
Chen, Y.6
Costa, E.7
Guidotti, A.8
Grayson, D.R.9
-
65
-
-
17444379438
-
Valproate corrects the schizophrenia-like epigenetic behavioral modifications induced by methionine in mice
-
Tremolizzo L, Doueiri MS, Dong E, Grayson DR, Davis J, Pinna G, Tueting P, Rodriguez-Menendez V, Costa E, Guidotti A. Valproate corrects the schizophrenia-like epigenetic behavioral modifications induced by methionine in mice. Biol Psychiatry 2005; 57: 500-9.
-
(2005)
Biol Psychiatry
, vol.57
, pp. 500-509
-
-
Tremolizzo, L.1
Doueiri, M.S.2
Dong, E.3
Grayson, D.R.4
Davis, J.5
Pinna, G.6
Tueting, P.7
Rodriguez-Menendez, V.8
Costa, E.9
Guidotti, A.10
-
66
-
-
20144373163
-
Hypermethylation of the reelin (RELN) promoter in the brain of schizophrenic patients: a preliminary report
-
Abdolmaleky HM, Cheng KH, Russo A, Smith CL, Faraone SV, Wilcox M, Shafa R, Glatt SJ, Nguyen G, Ponte JF, Thiagalingam S, Tsuang MT. Hypermethylation of the reelin (RELN) promoter in the brain of schizophrenic patients: a preliminary report. Am J Med Genet B Neuropsychiatr Genet. 2005; 134: 60-6.
-
(2005)
Am J Med Genet B Neuropsychiatr Genet.
, vol.134
, pp. 60-66
-
-
Abdolmaleky, H.M.1
Cheng, K.H.2
Russo, A.3
Smith, C.L.4
Faraone, S.V.5
Wilcox, M.6
Shafa, R.7
Glatt, S.J.8
Nguyen, G.9
Ponte, J.F.10
Thiagalingam, S.11
Tsuang, M.T.12
-
67
-
-
21544433777
-
Reelin promoter hypermethylation in schizophrenia
-
Grayson DR, Jia X, Chen Y, Sharma RP, Mitchell CP, Guidotti A, Costa E. Reelin promoter hypermethylation in schizophrenia. Proc Natl Acad Sci USA. 2005; 102: 9341-6.
-
(2005)
Proc Natl Acad Sci USA.
, vol.102
, pp. 9341-9346
-
-
Grayson, D.R.1
Jia, X.2
Chen, Y.3
Sharma, R.P.4
Mitchell, C.P.5
Guidotti, A.6
Costa, E.7
-
68
-
-
33750244045
-
Hypomethylation of MB-COMT promoter is a major risk factor for schizophrenia and bipolar disorder
-
Abdolmaleky HM, Cheng KH, Faraone SV, Wilcox M, Glatt SJ, Gao F, Smith CL, Shafa R, Aeali B, Carnevale J, Pan H, Papageorgis P, Ponte JF, Sivaraman V, Tsuang MT, Thiagalingam S. Hypomethylation of MB-COMT promoter is a major risk factor for schizophrenia and bipolar disorder. Hum Mol Genet. 2006; 15: 3132-45.
-
(2006)
Hum Mol Genet.
, vol.15
, pp. 3132-3145
-
-
Abdolmaleky, H.M.1
Cheng, K.H.2
Faraone, S.V.3
Wilcox, M.4
Glatt, S.J.5
Gao, F.6
Smith, C.L.7
Shafa, R.8
Aeali, B.9
Carnevale, J.10
Pan, H.11
Papageorgis, P.12
Ponte, J.F.13
Sivaraman, V.14
Tsuang, M.T.15
Thiagalingam, S.16
-
69
-
-
33646053801
-
Cognitive disruption and altered hippocampus synaptic function in Reelin haploin-sufficient mice
-
Qiu S, Korwek KM, Pratt-Davis AR, Peters M, Bergman MY, Weeber EJ. Cognitive disruption and altered hippocampus synaptic function in Reelin haploin-sufficient mice. Neurobiol Learn Mem. 2006; 85: 228-42.
-
(2006)
Neurobiol Learn Mem.
, vol.85
, pp. 228-242
-
-
Qiu, S.1
Korwek, K.M.2
Pratt-Davis, A.R.3
Peters, M.4
Bergman, M.Y.5
Weeber, E.J.6
-
70
-
-
0031570335
-
Construction of a 1.2-Mb contig surrounding, and molecular analysis of, the human CREB-binding protein (CBP/CREBBP) gene on chromosome 16p13.3
-
Giles RH, Petrij F, Dauwerse HG, den Hollander AI, Lushnikova T, van Ommen GJ, Goodman RH, Deaven LL, Doggett NA, Peters DJ, Breuning MH. Construction of a 1.2-Mb contig surrounding, and molecular analysis of, the human CREB-binding protein (CBP/CREBBP) gene on chromosome 16p13.3. Genomics 1997; 42: 96-114.
-
(1997)
Genomics
, vol.42
, pp. 96-114
-
-
Giles, R.H.1
Petrij, F.2
Dauwerse, H.G.3
den Hollander, A.I.4
Lushnikova, T.5
van Ommen, G.J.6
Goodman, R.H.7
Deaven, L.L.8
Doggett, N.A.9
Peters, D.J.10
Breuning, M.H.11
-
71
-
-
4143141116
-
Targeting CREB-binding protein (CBP) loss of function as a therapeutic strategy in neurological disorders
-
Rouaux C, Loeffler JP, Boutillier AL. Targeting CREB-binding protein (CBP) loss of function as a therapeutic strategy in neurological disorders. Biochem Pharmacol. 2004; 68: 1157-64.
-
(2004)
Biochem Pharmacol.
, vol.68
, pp. 1157-1164
-
-
Rouaux, C.1
Loeffler, J.P.2
Boutillier, A.L.3
-
72
-
-
20244366825
-
Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations
-
Petrij F, Dauwerse HG, Blough RI, Giles RH, van der Smagt JJ, Wallerstein R, Maaswinkel-Mooy PD, van Karnebeek CD, van Ommen GJ, van HA, Rubinstein JH, Saal HM, Hennekam RC, Peters DJ, Breuning MH. Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations. J Med Genet. 2000; 37: 168-76.
-
(2000)
J Med Genet.
, vol.37
, pp. 168-176
-
-
Petrij, F.1
Dauwerse, H.G.2
Blough, R.I.3
Giles, R.H.4
van der Smagt, J.J.5
Wallerstein, R.6
Maaswinkel-Mooy, P.D.7
van Karnebeek, C.D.8
van Ommen, G.J.9
van, H.A.10
Rubinstein, J.H.11
Saal, H.M.12
Hennekam, R.C.13
Peters, D.J.14
Breuning, M.H.15
-
73
-
-
24144501159
-
DNA sequencing of CREBBP demonstrates mutations in 56% of patients with Rubinstein-Taybi syndrome (RSTS) and in another patient with incomplete RSTS
-
Bartsch O, Schmidt S, Richter M, Morlot S, Seemanova E, Wiebe G, Rasi S. DNA sequencing of CREBBP demonstrates mutations in 56% of patients with Rubinstein-Taybi syndrome (RSTS) and in another patient with incomplete RSTS. Hum Genet. 2005; 117: 485-93.
-
(2005)
Hum Genet.
, vol.117
, pp. 485-493
-
-
Bartsch, O.1
Schmidt, S.2
Richter, M.3
Morlot, S.4
Seemanova, E.5
Wiebe, G.6
Rasi, S.7
-
74
-
-
0032216667
-
Rubinstein-Taybi syndrome. Review of 732 cases and analysis of the typical traits
-
Cantani A, Gagliesi D. Rubinstein-Taybi syndrome. Review of 732 cases and analysis of the typical traits. Eur Rev Med Pharmacol Sci. 1998; 2: 81-7.
-
(1998)
Eur Rev Med Pharmacol Sci.
, vol.2
, pp. 81-87
-
-
Cantani, A.1
Gagliesi, D.2
-
75
-
-
0031027626
-
Spaced training induces normal long-term memory in CREB mutant mice
-
Kogan JH, Frankland PW, Blendy JA, Coblentz J, Marowitz Z, Schutz G, Silva AJ. Spaced training induces normal long-term memory in CREB mutant mice. Curr Biol. 1997; 7: 1-11.
-
(1997)
Curr Biol.
, vol.7
, pp. 1-11
-
-
Kogan, J.H.1
Frankland, P.W.2
Blendy, J.A.3
Coblentz, J.4
Marowitz, Z.5
Schutz, G.6
Silva, A.J.7
-
76
-
-
0037075618
-
Molecular neurobiology of human cognition
-
Weeber EJ, Sweatt JD. Molecular neurobiology of human cognition. Neuron 2002; 33: 845-8.
-
(2002)
Neuron
, vol.33
, pp. 845-848
-
-
Weeber, E.J.1
Sweatt, J.D.2
-
77
-
-
33747140419
-
Rubinstein-Taybi syndrome: molecular findings and therapeutic approaches to improve cognitive dysfunction
-
Hallam TM, Bourtchouladze R. Rubinstein-Taybi syndrome: molecular findings and therapeutic approaches to improve cognitive dysfunction. Cell Mol Life Sci. 2006; 63: 1725-35.
-
(2006)
Cell Mol Life Sci.
, vol.63
, pp. 1725-1735
-
-
Hallam, T.M.1
Bourtchouladze, R.2
-
78
-
-
0034916613
-
p300/CBP proteins: HATs for transcriptional bridges and scaffolds
-
Chan HM, La Thangue NB p300/CBP proteins: HATs for transcriptional bridges and scaffolds. J Cell Sci. 2001; 114: 2363-73.
-
(2001)
J Cell Sci.
, vol.114
, pp. 2363-2373
-
-
Chan, H.M.1
La Thangue, N.B.2
-
79
-
-
4143098311
-
CBP and p300: HATs for different occasions
-
Kalkhoven E. CBP and p300: HATs for different occasions. Biochem Pharmacol. 2004; 68: 1145-55.
-
(2004)
Biochem Pharmacol.
, vol.68
, pp. 1145-1155
-
-
Kalkhoven, E.1
-
80
-
-
0033018277
-
Truncated CBP protein leads to classical Rubinstein-Taybi syndrome phenotypes in mice: implications for a dominant-negative mechanism
-
Oike Y, Hata A, Mamiya T, Kaname T, Noda Y, Suzuki M, Yasue H, Nabeshima T, Araki K, Yamamura K. Truncated CBP protein leads to classical Rubinstein-Taybi syndrome phenotypes in mice: implications for a dominant-negative mechanism. Hum Mol Genet. 1999; 8: 387-96.
-
(1999)
Hum Mol Genet.
, vol.8
, pp. 387-396
-
-
Oike, Y.1
Hata, A.2
Mamiya, T.3
Kaname, T.4
Noda, Y.5
Suzuki, M.6
Yasue, H.7
Nabeshima, T.8
Araki, K.9
Yamamura, K.10
-
81
-
-
0042337368
-
A mouse model of Rubinstein-Taybi syndrome: defective long-term memory is ameliorated by inhibitors of phosphodiesterase 4
-
Bourtchouladze R, Lidge R, Catapano R, Stanley J, Gossweiler S, Romashko D, Scott R, Tully T. A mouse model of Rubinstein-Taybi syndrome: defective long-term memory is ameliorated by inhibitors of phosphodiesterase 4. Proc Natl Acad Sci USA. 2003; 100: 10518-22.
-
(2003)
Proc Natl Acad Sci USA.
, vol.100
, pp. 10518-10522
-
-
Bourtchouladze, R.1
Lidge, R.2
Catapano, R.3
Stanley, J.4
Gossweiler, S.5
Romashko, D.6
Scott, R.7
Tully, T.8
-
82
-
-
0033613212
-
Insoluble detergent-resistant aggregates form between pathological and nonpathological lengths of polyglutamine in mammalian cells
-
Kazantsev A, Preisinger E, Dranovsky A, Goldgaber D, Housman D. Insoluble detergent-resistant aggregates form between pathological and nonpathological lengths of polyglutamine in mammalian cells. Proc Natl Acad Sci USA. 1999; 96: 11404-9.
-
(1999)
Proc Natl Acad Sci USA.
, vol.96
, pp. 11404-11409
-
-
Kazantsev, A.1
Preisinger, E.2
Dranovsky, A.3
Goldgaber, D.4
Housman, D.5
-
83
-
-
0035909999
-
Histone deacetylase inhibitors reduce polyglutamine toxicity
-
McCampbell A, Taye AA, Whitty L, Penney E, Steffan JS, Fischbeck KH. Histone deacetylase inhibitors reduce polyglutamine toxicity. Proc Natl Acad Sci USA. 2001; 98: 15179-84.
-
(2001)
Proc Natl Acad Sci USA.
, vol.98
, pp. 15179-15184
-
-
McCampbell, A.1
Taye, A.A.2
Whitty, L.3
Penney, E.4
Steffan, J.S.5
Fischbeck, K.H.6
-
84
-
-
0142157600
-
Histone deacetylase inhibition by sodium butyrate chemotherapy ameliorates the neurodegenerative phenotype in Huntington's disease mice
-
Ferrante RJ, Kubilus JK, Lee J, Ryu H, Beesen A, Zucker B, Smith K, Kowall NW, Ratan RR, Luthi-Carter R, Hersch SM. Histone deacetylase inhibition by sodium butyrate chemotherapy ameliorates the neurodegenerative phenotype in Huntington's disease mice. J Neurosci. 2003; 23: 9418-27.
-
(2003)
J Neurosci.
, vol.23
, pp. 9418-9427
-
-
Ferrante, R.J.1
Kubilus, J.K.2
Lee, J.3
Ryu, H.4
Beesen, A.5
Zucker, B.6
Smith, K.7
Kowall, N.W.8
Ratan, R.R.9
Luthi-Carter, R.10
Hersch, S.M.11
-
85
-
-
19944431703
-
Neuroprotective effects of phenylbutyrate in the N171-82Q transgenic mouse model of Huntington's disease
-
Gardian G, Browne SE, Choi DK, Klivenyi P, Gregorio J, Kubilus JK, Ryu H, Langley B, Ratan RR, Ferrante RJ, Beal MF. Neuroprotective effects of phenylbutyrate in the N171-82Q transgenic mouse model of Huntington's disease. J Biol Chem. 2005; 280: 556-63.
-
(2005)
J Biol Chem.
, vol.280
, pp. 556-563
-
-
Gardian, G.1
Browne, S.E.2
Choi, D.K.3
Klivenyi, P.4
Gregorio, J.5
Kubilus, J.K.6
Ryu, H.7
Langley, B.8
Ratan, R.R.9
Ferrante, R.J.10
Beal, M.F.11
-
86
-
-
17044439021
-
Alzheimer's disease: Abeta, tau and synaptic dysfunction
-
Laferla FM, Oddo S. Alzheimer's disease: Abeta, tau and synaptic dysfunction. Trends Mol Med. 2005; 11: 170-6.
-
(2005)
Trends Mol Med.
, vol.11
, pp. 170-176
-
-
Laferla, F.M.1
Oddo, S.2
-
88
-
-
33845328844
-
Synaptic dysfunction and oxidative stress in Alzheimer's disease: Emerging mechanisms
-
Forero DA, Casadesus G, Perry G, Arboleda H. Synaptic dysfunction and oxidative stress in Alzheimer's disease: Emerging mechanisms. J Cell Mol Med. 2006; 10: 796-805.
-
(2006)
J Cell Mol Med.
, vol.10
, pp. 796-805
-
-
Forero, D.A.1
Casadesus, G.2
Perry, G.3
Arboleda, H.4
-
89
-
-
0036792096
-
Amyloid beta -peptide inhibition of the PKA/CREB pathway and long-term potentiation: reversibility by drugs that enhance cAMP signaling
-
Vitolo OV, Sant'Angelo A, Costanzo V, Battaglia F, Arancio O, Shelanski M. Amyloid beta -peptide inhibition of the PKA/CREB pathway and long-term potentiation: reversibility by drugs that enhance cAMP signaling. Proc Natl Acad Sci USA. 2002; 99: 13217-21.
-
(2002)
Proc Natl Acad Sci USA.
, vol.99
, pp. 13217-13221
-
-
Vitolo, O.V.1
Sant'Angelo, A.2
Costanzo, V.3
Battaglia, F.4
Arancio, O.5
Shelanski, M.6
-
90
-
-
85047694516
-
Persistent improvement in synaptic and cognitive functions in an Alzheimer mouse model after rolipram treatment
-
Gong B, Vitolo OV, Trinchese F, Liu S, Shelanski M, Arancio O. Persistent improvement in synaptic and cognitive functions in an Alzheimer mouse model after rolipram treatment. J Clin Invest. 2004; 114: 1624-34.
-
(2004)
J Clin Invest.
, vol.114
, pp. 1624-1634
-
-
Gong, B.1
Vitolo, O.V.2
Trinchese, F.3
Liu, S.4
Shelanski, M.5
Arancio, O.6
-
91
-
-
33646261868
-
Nobiletin restoring beta-amyloid-impaired CREB phosphorylation rescues memory deterioration in Alzheimer's disease model rats
-
Matsuzaki K, Yamakuni T, Hashimoto M, Haque AM, Shido O, Mimaki Y, Sashida Y, Ohizumi Y. Nobiletin restoring beta-amyloid-impaired CREB phosphorylation rescues memory deterioration in Alzheimer's disease model rats. Neurosci Lett. 2006; 400: 230-4.
-
(2006)
Neurosci Lett.
, vol.400
, pp. 230-234
-
-
Matsuzaki, K.1
Yamakuni, T.2
Hashimoto, M.3
Haque, A.M.4
Shido, O.5
Mimaki, Y.6
Sashida, Y.7
Ohizumi, Y.8
-
92
-
-
11144354609
-
Loss of presenilin function causes impairments of memory and synaptic plasticity followed by age-dependent neurode-generation
-
Saura CA, Choi SY, Beglopoulos V, Malkani S, Zhang D, Shankaranarayana Rao BS, Chattarji S, Kelleher RJ, III, Kandel ER, Duff K, Kirkwood A, Shen J. Loss of presenilin function causes impairments of memory and synaptic plasticity followed by age-dependent neurode-generation. Neuron 2004; 42: 23-36.
-
(2004)
Neuron
, vol.42
, pp. 23-36
-
-
Saura, C.A.1
Choi, S.Y.2
Beglopoulos, V.3
Malkani, S.4
Zhang, D.5
Shankaranarayana Rao, B.S.6
Chattarji, S.7
Kelleher III, R.J.8
Kandel, E.R.9
Duff, K.10
Kirkwood, A.11
Shen, J.12
-
93
-
-
33745584643
-
Regulated intramembrane proteolysis of amyloid precursor protein and regulation of expression of putative target genes
-
Hebert SS, Serneels L, Tolia A, Craessaerts K, Derks C, Filippov MA, Muller U, De SB. Regulated intramembrane proteolysis of amyloid precursor protein and regulation of expression of putative target genes. EMBO Rep. 2006; 7: 739-45.
-
(2006)
EMBO Rep.
, vol.7
, pp. 739-745
-
-
Hebert, S.S.1
Serneels, L.2
Tolia, A.3
Craessaerts, K.4
Derks, C.5
Filippov, M.A.6
Muller, U.7
De, S.B.8
-
94
-
-
30344444484
-
Histone acetylation by Trrap-Tip60 modulates loading of repair proteins and repair of DNA double-strand breaks
-
Murr R, Loizou JI, Yang YG, Cuenin C, Li H, Wang ZQ, Herceg Z. Histone acetylation by Trrap-Tip60 modulates loading of repair proteins and repair of DNA double-strand breaks. Nat Cell Biol. 2006; 8: 91-9.
-
(2006)
Nat Cell Biol.
, vol.8
, pp. 91-99
-
-
Murr, R.1
Loizou, J.I.2
Yang, Y.G.3
Cuenin, C.4
Li, H.5
Wang, Z.Q.6
Herceg, Z.7
-
95
-
-
33745222513
-
The role of CREB in depression and antide-pressant treatment
-
Blendy JA. The role of CREB in depression and antide-pressant treatment. Biol Psychiatry. 2006; 59: 1144-50.
-
(2006)
Biol Psychiatry.
, vol.59
, pp. 1144-1150
-
-
Blendy, J.A.1
-
96
-
-
0037194790
-
Coordination of circadian timing in mammals
-
Reppert SM, Weaver DR. Coordination of circadian timing in mammals. Nature 2002; 418: 935-41.
-
(2002)
Nature
, vol.418
, pp. 935-941
-
-
Reppert, S.M.1
Weaver, D.R.2
-
97
-
-
33646145721
-
Circadian regulator CLOCK is a histone acetyltransferase
-
Doi M, Hirayama J, Sassone-Corsi P. Circadian regulator CLOCK is a histone acetyltransferase. Cell 2006; 125: 497-508.
-
(2006)
Cell
, vol.125
, pp. 497-508
-
-
Doi, M.1
Hirayama, J.2
Sassone-Corsi, P.3
-
98
-
-
3042589127
-
Histone modifications at gene promoter regions in rat hippocampus after acute and chronic electroconvulsive seizures
-
Tsankova NM, Kumar A, Nestler EJ. Histone modifications at gene promoter regions in rat hippocampus after acute and chronic electroconvulsive seizures. J Neurosci. 2004; 24: 5603-10.
-
(2004)
J Neurosci.
, vol.24
, pp. 5603-5610
-
-
Tsankova, N.M.1
Kumar, A.2
Nestler, E.J.3
-
99
-
-
33645774713
-
Histone modifications in status epilepticus induced by kainate
-
Taniura H, Sng JC, Yoneda Y. Histone modifications in status epilepticus induced by kainate. Histol Histopathol. 2006; 21: 785-91.
-
(2006)
Histol Histopathol.
, vol.21
, pp. 785-791
-
-
Taniura, H.1
Sng, J.C.2
Yoneda, Y.3
-
100
-
-
33645781251
-
CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene
-
Jongmans MC, Admiraal RJ, van der Donk KP, Vissers LE, Baas AF, Kapusta L, van Hagen JM, Donnai D, de Ravel TJ, Veltman JA, Geurts van KA, de Vries BB, Brunner HG, Hoefsloot LH, van Ravenswaaij CM. CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene. J Med Genet. 2006; 43: 306-14.
-
(2006)
J Med Genet.
, vol.43
, pp. 306-314
-
-
Jongmans, M.C.1
Admiraal, R.J.2
van der Donk, K.P.3
Vissers, L.E.4
Baas, A.F.5
Kapusta, L.6
van Hagen, J.M.7
Donnai, D.8
de Ravel, T.J.9
Veltman, J.A.10
Geurts van, K.A.11
de Vries, B.B.12
Brunner, H.G.13
Hoefsloot, L.H.14
van Ravenswaaij, C.M.15
-
101
-
-
4444239112
-
Mutations in a new member of the chromodomain gene family cause CHARGE syndrome
-
Vissers LE, van Ravenswaaij CM, Admiraal R, Hurst JA, de Vries BB, Janssen IM, Van D V, Huys EH, de Jong PJ, Hamel BC, Schoenmakers EF, Brunner HG, Veltman JA, van Kessel AG. Mutations in a new member of the chromodomain gene family cause CHARGE syndrome. Nat Genet. 2004; 36: 955-7.
-
(2004)
Nat Genet.
, vol.36
, pp. 955-957
-
-
Vissers, L.E.1
van Ravenswaaij, C.M.2
Admiraal, R.3
Hurst, J.A.4
de Vries, B.B.5
Janssen, I.M.6
Van, D.V.7
Huys, E.H.8
de Jong, P.J.9
Hamel, B.C.10
Schoenmakers, E.F.11
Brunner, H.G.12
Veltman, J.A.13
van Kessel, A.G.14
-
102
-
-
0030761277
-
Characterization of the CHD family of proteins
-
Woodage T, Basrai MA, Baxevanis AD, Hieter P, Collins FS. Characterization of the CHD family of proteins. Proc Natl Acad Sci USA. 1997; 94: 11472-7.
-
(1997)
Proc Natl Acad Sci USA.
, vol.94
, pp. 11472-11477
-
-
Woodage, T.1
Basrai, M.A.2
Baxevanis, A.D.3
Hieter, P.4
Collins, F.S.5
-
103
-
-
0031595103
-
Chromo-domain proteins: linking chromatin structure to epigenetic regulation
-
Cavalli G, Paro R. Chromo-domain proteins: linking chromatin structure to epigenetic regulation. Curr Opin Cell Biol. 1998; 10: 354-60.
-
(1998)
Curr Opin Cell Biol.
, vol.10
, pp. 354-360
-
-
Cavalli, G.1
Paro, R.2
-
104
-
-
2942631126
-
Localized domains of G9a-mediated histone methylation are required for silencing of neuronal genes
-
Roopra A, Qazi R, Schoenike B, Daley TJ, Morrison JF. Localized domains of G9a-mediated histone methylation are required for silencing of neuronal genes. Mol Cell. 2004; 14: 727-38.
-
(2004)
Mol Cell.
, vol.14
, pp. 727-738
-
-
Roopra, A.1
Qazi, R.2
Schoenike, B.3
Daley, T.J.4
Morrison, J.F.5
-
105
-
-
0037052539
-
A complex with chromatin modifiers that occupies E2F- and Myc-responsive genes in G0 cells
-
Ogawa H, Ishiguro K, Gaubatz S, Livingston DM, Nakatani Y. A complex with chromatin modifiers that occupies E2F- and Myc-responsive genes in G0 cells. Science 2002; 296: 1132-6.
-
(2002)
Science
, vol.296
, pp. 1132-1136
-
-
Ogawa, H.1
Ishiguro, K.2
Gaubatz, S.3
Livingston, D.M.4
Nakatani, Y.5
-
106
-
-
33746563985
-
Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome
-
Kleefstra T, Brunner HG, Amiel J, Oudakker AR, Nillesen WM, Magee A, Genevieve D, Cormier-Daire V, Van EH, Fryns JP, Hamel BC, Sistermans EA, de Vries BB, van BH. Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome. Am J Hum Genet. 2006; 79: 370-7.
-
(2006)
Am J Hum Genet.
, vol.79
, pp. 370-377
-
-
Kleefstra, T.1
Brunner, H.G.2
Amiel, J.3
Oudakker, A.R.4
Nillesen, W.M.5
Magee, A.6
Genevieve, D.7
Cormier-Daire, V.8
Van, E.H.9
Fryns, J.P.10
Hamel, B.C.11
Sistermans, E.A.12
de Vries, B.B.13
van, B.H.14
-
107
-
-
2542441563
-
The molecular basis of intellectual disability: novel genes with naturally occurring mutations causing altered gene expression in the brain
-
Gecz J. The molecular basis of intellectual disability: novel genes with naturally occurring mutations causing altered gene expression in the brain. Front Biosci. 2004; 9: 1-7.
-
(2004)
Front Biosci.
, vol.9
, pp. 1-7
-
-
Gecz, J.1
-
108
-
-
33646505092
-
X-linked mental retardation: many genes for a complex disorder
-
Ropers HH. X-linked mental retardation: many genes for a complex disorder. Curr Opin Genet Dev. 2006; 16: 260-9.
-
(2006)
Curr Opin Genet Dev.
, vol.16
, pp. 260-269
-
-
Ropers, H.H.1
-
109
-
-
0035464960
-
Monogenic causes of X-linked mental retardation
-
Chelly J, Mandel JL. Monogenic causes of X-linked mental retardation. Nat Rev Genet. 2001; 2: 669-80.
-
(2001)
Nat Rev Genet.
, vol.2
, pp. 669-680
-
-
Chelly, J.1
Mandel, J.L.2
-
110
-
-
28044451272
-
Advances in X-linked mental retardation
-
Stevenson RE. Advances in X-linked mental retardation. Curr Opin Pediatr. 2005; 17: 720-4.
-
(2005)
Curr Opin Pediatr.
, vol.17
, pp. 720-724
-
-
Stevenson, R.E.1
-
111
-
-
2942729593
-
High resolution profiling of X chromosomal aberrations by array comparative genomic hybridisation
-
Veltman JA, Yntema HG, Lugtenberg D, Arts H, Briault S, Huys EH, Osoegawa K, de Jong P, Brunner HG, Geurts vK, Van Bokhoven H, Schoenmakers EF. High resolution profiling of X chromosomal aberrations by array comparative genomic hybridisation. J Med Genet. 2004; 41: 425-32.
-
(2004)
J Med Genet.
, vol.41
, pp. 425-432
-
-
Veltman, J.A.1
Yntema, H.G.2
Lugtenberg, D.3
Arts, H.4
Briault, S.5
Huys, E.H.6
Osoegawa, K.7
de Jong, P.8
Brunner, H.G.9
Geurts, vK.10
Van Bokhoven, H.11
Schoenmakers, E.F.12
-
112
-
-
23944447954
-
X chromosome array-CGH for the identification of novel X-linked mental retardation genes
-
Bauters M, Van Esch H, Marynen P, Froyen G. X chromosome array-CGH for the identification of novel X-linked mental retardation genes. Eur J Med Genet. 2005; 48: 263-75.
-
(2005)
Eur J Med Genet.
, vol.48
, pp. 263-275
-
-
Bauters, M.1
Van Esch, H.2
Marynen, P.3
Froyen, G.4
-
113
-
-
23944517115
-
Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis
-
Van Esch H, Hollanders K, Badisco L, Melotte C, Van Hummelen P., Vermeesch JR, Devriendt K, Fryns JP, Marynen P, Froyen G. Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis. Hum Mol Genet. 2005; 14: 1795-803.
-
(2005)
Hum Mol Genet.
, vol.14
, pp. 1795-1803
-
-
Van Esch, H.1
Hollanders, K.2
Badisco, L.3
Melotte, C.4
Van Hummelen, P.5
Vermeesch, J.R.6
Devriendt, K.7
Fryns, J.P.8
Marynen, P.9
Froyen, G.10
-
114
-
-
23944503759
-
Duplication of the MECP2 Region Is a Frequent Cause of Severe Mental Retardation and Progressive Neurological Symptoms in Males
-
Van Esch H, Bauters M, Ignatius J, Jansen M, Raynaud M, Hollanders K, Lugtenberg D, Bienvenu T, Jensen LR, Gecz J, Moraine C, Marynen P, Fryns JP, Froyen G. Duplication of the MECP2 Region Is a Frequent Cause of Severe Mental Retardation and Progressive Neurological Symptoms in Males. Am J Hum Genet. 2005; 77: 442-53.
-
(2005)
Am J Hum Genet.
, vol.77
, pp. 442-453
-
-
Van Esch, H.1
Bauters, M.2
Ignatius, J.3
Jansen, M.4
Raynaud, M.5
Hollanders, K.6
Lugtenberg, D.7
Bienvenu, T.8
Jensen, L.R.9
Gecz, J.10
Moraine, C.11
Marynen, P.12
Fryns, J.P.13
Froyen, G.14
-
115
-
-
0025905795
-
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
-
Verkerk AJ, Pieretti M, Sutcliffe JS, Fu YH, Kuhl DP, Pizzuti A, Reiner O, Richards S, Victoria MF, Zhang FP. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell 1991; 65: 905-14.
-
(1991)
Cell
, vol.65
, pp. 905-914
-
-
Verkerk, A.J.1
Pieretti, M.2
Sutcliffe, J.S.3
Fu, Y.H.4
Kuhl, D.P.5
Pizzuti, A.6
Reiner, O.7
Richards, S.8
Victoria, M.F.9
Zhang, F.P.10
-
116
-
-
0026922707
-
DNA methylation represses FMR-1 transcription in fragile X syndrome
-
Sutcliffe JS, Nelson DL, Zhang F, Pieretti M, Caskey CT, Saxe D, Warren ST. DNA methylation represses FMR-1 transcription in fragile X syndrome. Hum Mol Genet. 1992; 1: 397-400.
-
(1992)
Hum Mol Genet.
, vol.1
, pp. 397-400
-
-
Sutcliffe, J.S.1
Nelson, D.L.2
Zhang, F.3
Pieretti, M.4
Caskey, C.T.5
Saxe, D.6
Warren, S.T.7
-
117
-
-
33745185532
-
mRNPs, polysomes or granules: FMRP in neuronal protein synthesis
-
Zalfa F, Achsel T, Bagni C. mRNPs, polysomes or granules: FMRP in neuronal protein synthesis. Curr Opin Neurobiol. 2006; 16: 265-9.
-
(2006)
Curr Opin Neurobiol.
, vol.16
, pp. 265-269
-
-
Zalfa, F.1
Achsel, T.2
Bagni, C.3
-
118
-
-
0032905253
-
Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells
-
Coffee B, Zhang F, Warren ST, Reines D. Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells. Nat Genet. 1999; 22: 98-101.
-
(1999)
Nat Genet.
, vol.22
, pp. 98-101
-
-
Coffee, B.1
Zhang, F.2
Warren, S.T.3
Reines, D.4
-
119
-
-
0036782129
-
Histone modifications depict an aberrantly heterochroma-tinized FMR1 gene in fragile x syndrome
-
Coffee B, Zhang F, Ceman S, Warren ST, Reines D. Histone modifications depict an aberrantly heterochroma-tinized FMR1 gene in fragile x syndrome. Am J Hum Genet. 2002; 71: 923-32.
-
(2002)
Am J Hum Genet.
, vol.71
, pp. 923-932
-
-
Coffee, B.1
Zhang, F.2
Ceman, S.3
Warren, S.T.4
Reines, D.5
-
120
-
-
33747591451
-
The active FMR1 promoter is associated with a large domain of altered chromatin conformation with embedded local histone modifications
-
Gheldof N, Tabuchi TM, Dekker J. The active FMR1 promoter is associated with a large domain of altered chromatin conformation with embedded local histone modifications. Proc Natl Acad Sci USA. 2006; 103: 12463-8.
-
(2006)
Proc Natl Acad Sci USA.
, vol.103
, pp. 12463-12468
-
-
Gheldof, N.1
Tabuchi, T.M.2
Dekker, J.3
-
121
-
-
19944431036
-
Molecular dissection of the events leading to inactivation of the FMR1 gene
-
Pietrobono R, Tabolacci E, Zalfa F, Zito I, Terracciano A, Moscato U, Bagni C, Oostra B, Chiurazzi P, Neri G. Molecular dissection of the events leading to inactivation of the FMR1 gene. Hum Mol Genet. 2005; 14: 267-77.
-
(2005)
Hum Mol Genet.
, vol.14
, pp. 267-277
-
-
Pietrobono, R.1
Tabolacci, E.2
Zalfa, F.3
Zito, I.4
Terracciano, A.5
Moscato, U.6
Bagni, C.7
Oostra, B.8
Chiurazzi, P.9
Neri, G.10
-
122
-
-
24344457816
-
Suppression of two major Fragile X Syndrome mouse model phenotypes by the mGluR5 antagonist MPEP
-
Yan QJ, Rammal M, Tranfaglia M, Bauchwitz RP. Suppression of two major Fragile X Syndrome mouse model phenotypes by the mGluR5 antagonist MPEP. Neuropharmacology 2005; 49: 1053-66.
-
(2005)
Neuropharmacology
, vol.49
, pp. 1053-1066
-
-
Yan, Q.J.1
Rammal, M.2
Tranfaglia, M.3
Bauchwitz, R.P.4
-
123
-
-
20044388322
-
Pharmacological rescue of synaptic plasticity, courtship behavior, and mushroom body defects in a Drosophila model of fragile X syndrome
-
McBride SM, Choi CH, Wang Y, Liebelt D, Braunstein E, Ferreiro D, Sehgal A, Siwicki KK, Dockendorff TC, Nguyen HT, McDonald TV, Jongens TA. Pharmacological rescue of synaptic plasticity, courtship behavior, and mushroom body defects in a Drosophila model of fragile X syndrome. Neuron 2005; 45: 753-64.
-
(2005)
Neuron
, vol.45
, pp. 753-764
-
-
McBride, S.M.1
Choi, C.H.2
Wang, Y.3
Liebelt, D.4
Braunstein, E.5
Ferreiro, D.6
Sehgal, A.7
Siwicki, K.K.8
Dockendorff, T.C.9
Nguyen, H.T.10
McDonald, T.V.11
Jongens, T.A.12
-
124
-
-
0029038394
-
Molecular and neurobiology aspects of Rett syndrome
-
Hanefeld F, Hagberg B, Percy A. Molecular and neurobiology aspects of Rett syndrome. Neuropediatrics 1995; 26: 60-1.
-
(1995)
Neuropediatrics
, vol.26
, pp. 60-61
-
-
Hanefeld, F.1
Hagberg, B.2
Percy, A.3
-
125
-
-
0037002625
-
An update on clinically applicable diagnostic criteria in Rett syndrome. Comments to Rett Syndrome clinical criteria consensus panel satellite to European paediatric neurology Society meeting, Baden Baden, Germany, 11 September 2001
-
Hagberg B, Hanefeld F, Percy A, Skjeldal O. An update on clinically applicable diagnostic criteria in Rett syndrome. Comments to Rett Syndrome clinical criteria consensus panel satellite to European paediatric neurology Society meeting, Baden Baden, Germany, 11 September 2001. Eur J Paediatr Neurol. 2002; 6: 293-7.
-
(2002)
Eur J Paediatr Neurol.
, vol.6
, pp. 293-297
-
-
Hagberg, B.1
Hanefeld, F.2
Percy, A.3
Skjeldal, O.4
-
126
-
-
1642367538
-
Rett syndrome: a prototypical neu-rodevelopmental disorder
-
Neul JL, Zoghbi HY. Rett syndrome: a prototypical neu-rodevelopmental disorder. Neuroscientist 2004; 10: 118-28.
-
(2004)
Neuroscientist
, vol.10
, pp. 118-128
-
-
Neul, J.L.1
Zoghbi, H.Y.2
-
127
-
-
8444253290
-
Mild overexpression of MeCP2 causes a progressive neurological disorder in mice
-
Collins AL, Levenson JM, Vilaythong AP, Richman R, Armstrong DL, Noebels JL, David SJ, Zoghbi HY. Mild overexpression of MeCP2 causes a progressive neurological disorder in mice. Hum Mol Genet. 2004; 13: 2679-89.
-
(2004)
Hum Mol Genet.
, vol.13
, pp. 2679-2689
-
-
Collins, A.L.1
Levenson, J.M.2
Vilaythong, A.P.3
Richman, R.4
Armstrong, D.L.5
Noebels, J.L.6
David, S.J.7
Zoghbi, H.Y.8
-
129
-
-
33646893456
-
Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized
-
Bienvenu T, Chelly J. Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized. Nat Rev Genet. 2006; 7: 415-26.
-
(2006)
Nat Rev Genet.
, vol.7
, pp. 415-426
-
-
Bienvenu, T.1
Chelly, J.2
-
130
-
-
0242300612
-
DNA methylation-related chromatin remodeling in activity-dependent BDNF gene regulation
-
Martinowich K, Hattori D, Wu H, Fouse S, He F, Hu Y, Fan G, Sun YE. DNA methylation-related chromatin remodeling in activity-dependent BDNF gene regulation. Science 2003; 302: 890-3.
-
(2003)
Science
, vol.302
, pp. 890-893
-
-
Martinowich, K.1
Hattori, D.2
Wu, H.3
Fouse, S.4
He, F.5
Hu, Y.6
Fan, G.7
Sun, Y.E.8
-
131
-
-
0242332183
-
Derepression of BDNF transcription involves calcium-dependent phos-phorylation of MeCP2
-
Chen WG, Chang Q, Lin Y, Meissner A, West AE, Griffith EC, Jaenisch R, Greenberg ME. Derepression of BDNF transcription involves calcium-dependent phos-phorylation of MeCP2. Science 2003; 302: 885-9.
-
(2003)
Science
, vol.302
, pp. 885-889
-
-
Chen, W.G.1
Chang, Q.2
Lin, Y.3
Meissner, A.4
West, A.E.5
Griffith, E.C.6
Jaenisch, R.7
Greenberg, M.E.8
-
132
-
-
14044252235
-
Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3
-
Samaco RC, Hogart A, LaSalle JM. Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3. Hum Mol Genet. 2005; 14: 483-92.
-
(2005)
Hum Mol Genet.
, vol.14
, pp. 483-492
-
-
Samaco, R.C.1
Hogart, A.2
LaSalle, J.M.3
-
133
-
-
17744380972
-
MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression
-
Makedonski K, Abuhatzira L, Kaufman Y, Razin A, Shemer R. MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression. Hum Mol Genet. 2005; 14: 1049-58.
-
(2005)
Hum Mol Genet.
, vol.14
, pp. 1049-1058
-
-
Makedonski, K.1
Abuhatzira, L.2
Kaufman, Y.3
Razin, A.4
Shemer, R.5
-
134
-
-
26444516160
-
Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome
-
Nuber UA, Kriaucionis S, Roloff TC, Guy J, Selfridge J, Steinhoff C, Schulz R, Lipkowitz B, Ropers HH, Holmes MC, Bird A. Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome. Hum Mol Genet. 2005; 14: 2247-56.
-
(2005)
Hum Mol Genet.
, vol.14
, pp. 2247-2256
-
-
Nuber, U.A.1
Kriaucionis, S.2
Roloff, T.C.3
Guy, J.4
Selfridge, J.5
Steinhoff, C.6
Schulz, R.7
Lipkowitz, B.8
Ropers, H.H.9
Holmes, M.C.10
Bird, A.11
-
135
-
-
11244328520
-
Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome
-
Horike S, Cai S, Miyano M, Cheng JF, Kohwi-Shigematsu T. Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome. Nat Genet. 2005; 37: 31-40.
-
(2005)
Nat Genet.
, vol.37
, pp. 31-40
-
-
Horike, S.1
Cai, S.2
Miyano, M.3
Cheng, J.F.4
Kohwi-Shigematsu, T.5
-
136
-
-
33745479882
-
Gene expression analysis exposes mitochondrial abnormalities in a mouse model of Rett syndrome
-
Kriaucionis S, Paterson A, Curtis J, Guy J, Macleod N, Bird A. Gene expression analysis exposes mitochondrial abnormalities in a mouse model of Rett syndrome. Mol Cell Biol. 2006; 26: 5033-42.
-
(2006)
Mol Cell Biol.
, vol.26
, pp. 5033-5042
-
-
Kriaucionis, S.1
Paterson, A.2
Curtis, J.3
Guy, J.4
Macleod, N.5
Bird, A.6
-
137
-
-
33745609276
-
Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndrome
-
Peddada S, Yasui DH, LaSalle JM. Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndrome. Hum Mol Genet. 2006; 15: 2003-14.
-
(2006)
Hum Mol Genet.
, vol.15
, pp. 2003-2014
-
-
Peddada, S.1
Yasui, D.H.2
LaSalle, J.M.3
-
138
-
-
0035160042
-
Gene expression profiling in postmortem Rett Syndrome brain: differential gene expression and patient classification
-
Colantuoni C, Jeon OH, Hyder K, Chenchik A, Khimani AH, Narayanan V, Hoffman EP, Kaufmann WE, Naidu S, Pevsner J. Gene expression profiling in postmortem Rett Syndrome brain: differential gene expression and patient classification. Neurobiol Dis. 2001; 8: 847-65.
-
(2001)
Neurobiol Dis.
, vol.8
, pp. 847-865
-
-
Colantuoni, C.1
Jeon, O.H.2
Hyder, K.3
Chenchik, A.4
Khimani, A.H.5
Narayanan, V.6
Hoffman, E.P.7
Kaufmann, W.E.8
Naidu, S.9
Pevsner, J.10
-
139
-
-
0035192518
-
Neurobiology of Rett syndrome: a genetic disorder of synapse development
-
Johnston MV, Jeon OH, Pevsner J, Blue ME, Naidu S. Neurobiology of Rett syndrome: a genetic disorder of synapse development. Brain Dev. 2001; 23: S206-13.
-
(2001)
Brain Dev.
, vol.23
-
-
Johnston, M.V.1
Jeon, O.H.2
Pevsner, J.3
Blue, M.E.4
Naidu, S.5
-
140
-
-
0028939603
-
Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome)
-
Gibbons RJ, Picketts DJ, Villard L, Higgs DR. Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome). Cell 1995; 80: 837-45.
-
(1995)
Cell
, vol.80
, pp. 837-845
-
-
Gibbons, R.J.1
Picketts, D.J.2
Villard, L.3
Higgs, D.R.4
-
141
-
-
0031922879
-
Specific interaction between the XNP/AsTR-X gene product and the SET domain of the human EZH2 protein
-
Cardoso C, Timsit S, Villard L, Khrestchatisky M, Fontes M, Colleaux L. Specific interaction between the XNP/AsTR-X gene product and the SET domain of the human EZH2 protein. Hum Mol Genet. 1998; 7: 679-84.
-
(1998)
Hum Mol Genet.
, vol.7
, pp. 679-684
-
-
Cardoso, C.1
Timsit, S.2
Villard, L.3
Khrestchatisky, M.4
Fontes, M.5
Colleaux, L.6
-
142
-
-
14944359718
-
The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis
-
Berube NG, Mangelsdorf M, Jagla M, Vanderluit J, Garrick D, Gibbons RJ, Higgs DR, Slack RS, Picketts DJ. The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis. J Clin Invest. 2005; 115: 258-67.
-
(2005)
J Clin Invest.
, vol.115
, pp. 258-267
-
-
Berube, N.G.1
Mangelsdorf, M.2
Jagla, M.3
Vanderluit, J.4
Garrick, D.5
Gibbons, R.J.6
Higgs, D.R.7
Slack, R.S.8
Picketts, D.J.9
-
143
-
-
0141703327
-
The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies
-
Xue Y, Gibbons R, Yan Z, Yang D, McDowell TL, Sechi S, Qin J, Zhou S, Higgs D, Wang W. The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies. Proc Natl Acad Sci USA. 2003; 100: 10635-40.
-
(2003)
Proc Natl Acad Sci USA.
, vol.100
, pp. 10635-10640
-
-
Xue, Y.1
Gibbons, R.2
Yan, Z.3
Yang, D.4
McDowell, T.L.5
Sechi, S.6
Qin, J.7
Zhou, S.8
Higgs, D.9
Wang, W.10
-
144
-
-
0034069652
-
Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation
-
Gibbons RJ, McDowell TL, Raman S, O'Rourke DM, Garrick D, Ayyub H, Higgs DR. Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation. Nat Genet. 2000; 24: 368-71.
-
(2000)
Nat Genet.
, vol.24
, pp. 368-371
-
-
Gibbons, R.J.1
McDowell, T.L.2
Raman, S.3
O'Rourke, D.M.4
Garrick, D.5
Ayyub, H.6
Higgs, D.R.7
-
145
-
-
33646473832
-
Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues
-
Garrick D, Sharpe JA, Arkell R, Dobbie L, Smith AJ, Wood WG, Higgs DR, Gibbons RJ. Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues. PLoS Genet. 2006; 2: e58.
-
(2006)
PLoS Genet.
, vol.2
-
-
Garrick, D.1
Sharpe, J.A.2
Arkell, R.3
Dobbie, L.4
Smith, A.J.5
Wood, W.G.6
Higgs, D.R.7
Gibbons, R.J.8
-
146
-
-
0036793859
-
Coffin-Lowry syndrome: clinical and molecular features
-
Hanauer A, Young ID. Coffin-Lowry syndrome: clinical and molecular features. J Med Genet. 2002; 39: 705-13.
-
(2002)
J Med Genet.
, vol.39
, pp. 705-713
-
-
Hanauer, A.1
Young, I.D.2
-
147
-
-
0033529706
-
Requirement of Rsk-2 for epidermal growth factor-activated phosphorylation of histone H3
-
Sassone-Corsi P, Mizzen CA, Cheung P, Crosio C, Monaco L, Jacquot S, Hanauer A, Allis CD. Requirement of Rsk-2 for epidermal growth factor-activated phosphorylation of histone H3. Science 1999; 285: 886-91.
-
(1999)
Science
, vol.285
, pp. 886-891
-
-
Sassone-Corsi, P.1
Mizzen, C.A.2
Cheung, P.3
Crosio, C.4
Monaco, L.5
Jacquot, S.6
Hanauer, A.7
Allis, C.D.8
-
148
-
-
0032514734
-
Rsk-2 activity is necessary for epidermal growth factor-induced phosphorylation of CREB protein and transcription of c-fos gene
-
De Cesare D, Jacquot S, Hanauer A, Sassone-Corsi P. Rsk-2 activity is necessary for epidermal growth factor-induced phosphorylation of CREB protein and transcription of c-fos gene. Proc Natl Acad Sci USA. 1998; 95: 12202-7.
-
(1998)
Proc Natl Acad Sci USA.
, vol.95
, pp. 12202-12207
-
-
De Cesare, D.1
Jacquot, S.2
Hanauer, A.3
Sassone-Corsi, P.4
-
149
-
-
0034813107
-
Mitogen-regulated RSK2-CBP interaction controls their kinase and acetylase activities
-
Merienne K, Pannetier S, Harel-Bellan A, Sassone-Corsi P. Mitogen-regulated RSK2-CBP interaction controls their kinase and acetylase activities. Mol Cell Biol. 2001; 21: 7089-96.
-
(2001)
Mol Cell Biol.
, vol.21
, pp. 7089-7096
-
-
Merienne, K.1
Pannetier, S.2
Harel-Bellan, A.3
Sassone-Corsi, P.4
-
150
-
-
0037370029
-
Cascade of distinct histone modifications during collage-nase gene activation
-
Martens JH, Verlaan M, Kalkhoven E, Zantema A. Cascade of distinct histone modifications during collage-nase gene activation. Mol Cell Biol. 2003; 23: 1808-16.
-
(2003)
Mol Cell Biol.
, vol.23
, pp. 1808-1816
-
-
Martens, J.H.1
Verlaan, M.2
Kalkhoven, E.3
Zantema, A.4
-
151
-
-
19944430270
-
Mutations in the JARIDIC gene, which is involved in transcriptional regulation and chromatin remodeling, cause X-linked mental retardation
-
Jensen LR, Amende M, Gurok U, Moser B, Gimmel V, Tzschach A, Janecke AR, Tariverdian G, Chelly J, Fryns JP, Van Esch H, Kleefstra T, Hamel B, Moraine C, Gecz J, Turner G, Reinhardt R, Kalscheuer VM, Ropers HH, Lenzner S. Mutations in the JARIDIC gene, which is involved in transcriptional regulation and chromatin remodeling, cause X-linked mental retardation. Am J Hum Genet. 2005; 76: 227-36.
-
(2005)
Am J Hum Genet.
, vol.76
, pp. 227-236
-
-
Jensen, L.R.1
Amende, M.2
Gurok, U.3
Moser, B.4
Gimmel, V.5
Tzschach, A.6
Janecke, A.R.7
Tariverdian, G.8
Chelly, J.9
Fryns, J.P.10
Van Esch, H.11
Kleefstra, T.12
Hamel, B.13
Moraine, C.14
Gecz, J.15
Turner, G.16
Reinhardt, R.17
Kalscheuer, V.M.18
Ropers, H.H.19
Lenzner, S.20
more..
-
152
-
-
9144230687
-
Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation
-
Shoichet SA, Hoffmann K, Menzel C, Trautmann U, Moser B, Hoeltzenbein M, Echenne B, Partington M, van BH, Moraine C, Fryns JP, Chelly J, Rott HD, Ropers HH, Kalscheuer VM. Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation. Am J Hum Genet. 2003; 73: 1341-54.
-
(2003)
Am J Hum Genet.
, vol.73
, pp. 1341-1354
-
-
Shoichet, S.A.1
Hoffmann, K.2
Menzel, C.3
Trautmann, U.4
Moser, B.5
Hoeltzenbein, M.6
Echenne, B.7
Partington, M.8
van, B.H.9
Moraine, C.10
Fryns, J.P.11
Chelly, J.12
Rott, H.D.13
Ropers, H.H.14
Kalscheuer, V.M.15
-
153
-
-
2342535716
-
Zinc finger 81 (ZNF81) mutations associated with X-linked mental retardation
-
Kleefstra T, Yntema HG, Oudakker AR, Banning MJ, Kalscheuer VM, Chelly J, Moraine C, Ropers HH, Fryns JP, Janssen IM, Sistermans EA, Nillesen WN, de Vries LB, Hamel BC, van BH. Zinc finger 81 (ZNF81) mutations associated with X-linked mental retardation. J Med Genet. 2004; 41: 394-9.
-
(2004)
J Med Genet.
, vol.41
, pp. 394-399
-
-
Kleefstra, T.1
Yntema, H.G.2
Oudakker, A.R.3
Banning, M.J.4
Kalscheuer, V.M.5
Chelly, J.6
Moraine, C.7
Ropers, H.H.8
Fryns, J.P.9
Janssen, I.M.10
Sistermans, E.A.11
Nillesen, W.N.12
de Vries, L.B.13
Hamel, B.C.14
van, B.H.15
-
154
-
-
31544453949
-
ZNF674: A new Kruppel-associated box-containing zinc-finger gene involved in nonsyndromic X-linked mental retardation
-
Lugtenberg D, Yntema HG, Banning MJ, Oudakker AR, Firth HV, Willatt L, Raynaud M, Kleefstra T, Fryns JP, Ropers HH, Chelly J, Moraine C, Gecz J, Reeuwijk J, Nabuurs SB, de Vries BB, Hamel BC, de Brouwer AP, Bokhoven H. ZNF674: A new Kruppel-associated box-containing zinc-finger gene involved in nonsyndromic X-linked mental retardation. Am J Hum Genet. 2006; 78: 265-78.
-
(2006)
Am J Hum Genet.
, vol.78
, pp. 265-278
-
-
Lugtenberg, D.1
Yntema, H.G.2
Banning, M.J.3
Oudakker, A.R.4
Firth, H.V.5
Willatt, L.6
Raynaud, M.7
Kleefstra, T.8
Fryns, J.P.9
Ropers, H.H.10
Chelly, J.11
Moraine, C.12
Gecz, J.13
Reeuwijk, J.14
Nabuurs, S.B.15
de Vries, B.B.16
Hamel, B.C.17
de Brouwer, A.P.18
Bokhoven, H.19
-
155
-
-
0037089626
-
SETDB1: a novel KAP-1-associated histone H3, lysine 9-specific methyltransferase that contributes to HP1-mediated silencing of euchromatic genes by KRAB zinc-finger proteins
-
Schultz DC, Ayyanathan K, Negorev D, Maul GG, Rauscher FJ, III SETDB1: a novel KAP-1-associated histone H3, lysine 9-specific methyltransferase that contributes to HP1-mediated silencing of euchromatic genes by KRAB zinc-finger proteins. Genes Dev. 2002; 16: 919-32.
-
(2002)
Genes Dev.
, vol.16
, pp. 919-932
-
-
Schultz, D.C.1
Ayyanathan, K.2
Negorev, D.3
Maul, G.G.4
Rauscher III, F.J.5
-
156
-
-
33751007001
-
-
The KAP1 core-pressor functions to coordinate the assembly of de novo HP1 demarcated microenvironments of heterochromatin required for KRAB zinc finger protein mediated transcrip-tional repression. Mol Cell Biol.; Epub ahead of publication.
-
Sripathy SP, Stevens J, Schultz DC. The KAP1 core-pressor functions to coordinate the assembly of de novo HP1 demarcated microenvironments of heterochromatin required for KRAB zinc finger protein mediated transcrip-tional repression. Mol Cell Biol. 2006; Epub ahead of publication.
-
(2006)
-
-
Sripathy, S.P.1
Stevens, J.2
Schultz, D.C.3
-
157
-
-
12144287606
-
Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR
-
Ng D, Thakker N, Corcoran CM, Donnai D, Perveen R, Schneider A, Hadley DW, Tifft C, Zhang L, Wilkie AO, van der Smagt JJ, Gorlin RJ, Burgess SM, Bardwell VJ, Black GC, Biesecker LG. Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR. Nat Genet. 2004; 36: 411-6.
-
(2004)
Nat Genet.
, vol.36
, pp. 411-416
-
-
Ng, D.1
Thakker, N.2
Corcoran, C.M.3
Donnai, D.4
Perveen, R.5
Schneider, A.6
Hadley, D.W.7
Tifft, C.8
Zhang, L.9
Wilkie, A.O.10
van der Smagt, J.J.11
Gorlin, R.J.12
Burgess, S.M.13
Bardwell, V.J.14
Black, G.C.15
Biesecker, L.G.16
-
158
-
-
21044433480
-
Histone modifications: from genome-wide maps to functional insights
-
van LF, van SB. Histone modifications: from genome-wide maps to functional insights. Genome Biol. 2005; 6: 113.
-
(2005)
Genome Biol.
, vol.6
, pp. 113
-
-
van, L.F.1
van, S.B.2
-
159
-
-
20044384522
-
Mapping of genetic and epigenetic regulatory networks using microarrays
-
van Steensel B. Mapping of genetic and epigenetic regulatory networks using microarrays. Nat Genet. 2005; 37: S18-24.
-
(2005)
Nat Genet.
, vol.37
-
-
van Steensel, B.1
-
160
-
-
0032845039
-
Mi-2 complex couples DNA methylation to chromatin remodelling and histone deacetylation
-
Wade PA, Gegonne A, Jones PL, Ballestar E, Aubry F, Wolffe AP. Mi-2 complex couples DNA methylation to chromatin remodelling and histone deacetylation. Nat Genet. 1999; 23: 62-6.
-
(1999)
Nat Genet.
, vol.23
, pp. 62-66
-
-
Wade, P.A.1
Gegonne, A.2
Jones, P.L.3
Ballestar, E.4
Aubry, F.5
Wolffe, A.P.6
-
161
-
-
4344685735
-
Methyl-CpG binding protein MBD1 couples histone H3 methylation at lysine 9 by SETDB1 to DNA replication and chromatin assembly
-
Sarraf SA, Stancheva I. Methyl-CpG binding protein MBD1 couples histone H3 methylation at lysine 9 by SETDB1 to DNA replication and chromatin assembly. Mol Cell. 2004; 15: 595-605.
-
(2004)
Mol Cell.
, vol.15
, pp. 595-605
-
-
Sarraf, S.A.1
Stancheva, I.2
-
162
-
-
22244478317
-
Histone modifications in Rett syndrome lymphocytes: a preliminary evaluation
-
Kaufmann WE, Jarrar MH, Wang JS, Lee YJ, Reddy S, Bibat G, Naidu S. Histone modifications in Rett syndrome lymphocytes: a preliminary evaluation. Brain Dev. 2005; 27: 331-9.
-
(2005)
Brain Dev.
, vol.27
, pp. 331-339
-
-
Kaufmann, W.E.1
Jarrar, M.H.2
Wang, J.S.3
Lee, Y.J.4
Reddy, S.5
Bibat, G.6
Naidu, S.7
-
163
-
-
0037672689
-
An epigenetic road map for histone lysine methylation
-
Lachner M, O'Sullivan RJ, Jenuwein T. An epigenetic road map for histone lysine methylation. J Cell Sci. 2003; 116: 2117-24.
-
(2003)
J Cell Sci.
, vol.116
, pp. 2117-2124
-
-
Lachner, M.1
O'Sullivan, R.J.2
Jenuwein, T.3
-
164
-
-
31144432001
-
Epigenomics: mapping the methylome
-
Wilson IM, Davies JJ, Weber M, Brown CJ, Alvarez CE, MacAulay C, Schubeler D, Lam WL. Epigenomics: mapping the methylome. Cell Cycle 2006; 5: 155-8.
-
(2006)
Cell Cycle
, vol.5
, pp. 155-158
-
-
Wilson, I.M.1
Davies, J.J.2
Weber, M.3
Brown, C.J.4
Alvarez, C.E.5
MacAulay, C.6
Schubeler, D.7
Lam, W.L.8
-
165
-
-
21144457070
-
CpG Island microarray probe sequences derived from a physical library are representative of CpG Islands annotated on the human genome
-
Heisler LE, Torti D, Boutros PC, Watson J, Chan C, Winegarden N, Takahashi M, Yau P, Huang TH, Farnham PJ, Jurisica I, Woodgett JR, Bremner R, Penn LZ, Der SD. CpG Island microarray probe sequences derived from a physical library are representative of CpG Islands annotated on the human genome. Nucleic Acids Res. 2005; 33: 2952-61.
-
(2005)
Nucleic Acids Res.
, vol.33
, pp. 2952-2961
-
-
Heisler, L.E.1
Torti, D.2
Boutros, P.C.3
Watson, J.4
Chan, C.5
Winegarden, N.6
Takahashi, M.7
Yau, P.8
Huang, T.H.9
Farnham, P.J.10
Jurisica, I.11
Woodgett, J.R.12
Bremner, R.13
Penn, L.Z.14
Der, S.D.15
-
166
-
-
23044514626
-
Chromosome-wide and promoter-specific analyses identify sites of differential DNA methylation in normal and transformed human cells
-
Weber M, Davies JJ, Wittig D, Oakeley EJ, Haase M, Lam WL, Schubeler D. Chromosome-wide and promoter-specific analyses identify sites of differential DNA methylation in normal and transformed human cells. Nat Genet. 2005; 37: 853-62.
-
(2005)
Nat Genet.
, vol.37
, pp. 853-862
-
-
Weber, M.1
Davies, J.J.2
Wittig, D.3
Oakeley, E.J.4
Haase, M.5
Lam, W.L.6
Schubeler, D.7
-
167
-
-
13844313862
-
Whole-genome patterns of common DNA variation in three human populations
-
Hinds DA, Stuve LL, Nilsen GB, Halperin E, Eskin E, Ballinger DG, Frazer KA, Cox DR. Whole-genome patterns of common DNA variation in three human populations. Science 2005; 307: 1072-9.
-
(2005)
Science
, vol.307
, pp. 1072-1079
-
-
Hinds, D.A.1
Stuve, L.L.2
Nilsen, G.B.3
Halperin, E.4
Eskin, E.5
Ballinger, D.G.6
Frazer, K.A.7
Cox, D.R.8
-
168
-
-
29444457877
-
Common deletion polymorphisms in the human genome
-
McCarroll SA, Hadnott TN, Perry GH, Sabeti PC, Zody MC, Barrett JC, Dallaire S, Gabriel SB, Lee C, Daly MJ, Altshuler DM. Common deletion polymorphisms in the human genome. Nat Genet. 2006; 38: 86-92.
-
(2006)
Nat Genet.
, vol.38
, pp. 86-92
-
-
McCarroll, S.A.1
Hadnott, T.N.2
Perry, G.H.3
Sabeti, P.C.4
Zody, M.C.5
Barrett, J.C.6
Dallaire, S.7
Gabriel, S.B.8
Lee, C.9
Daly, M.J.10
Altshuler, D.M.11
-
169
-
-
29444450702
-
Common deletions and SNPs are in linkage disequilibrium in the human genome
-
Hinds DA, Kloek AP, Jen M, Chen X, Frazer KA. Common deletions and SNPs are in linkage disequilibrium in the human genome. Nat Genet. 2006; 38: 82-5.
-
(2006)
Nat Genet.
, vol.38
, pp. 82-85
-
-
Hinds, D.A.1
Kloek, A.P.2
Jen, M.3
Chen, X.4
Frazer, K.A.5
-
170
-
-
29444441336
-
A high-resolution survey of deletion polymorphism in the human genome
-
Conrad DF, Andrews TD, Carter NP, Hurles ME, Pritchard JK. A high-resolution survey of deletion polymorphism in the human genome. Nat Genet. 2006; 38: 75-81.
-
(2006)
Nat Genet.
, vol.38
, pp. 75-81
-
-
Conrad, D.F.1
Andrews, T.D.2
Carter, N.P.3
Hurles, M.E.4
Pritchard, J.K.5
|