-
1
-
-
0031837109
-
Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription
-
Jones, P.L., Veenstra, G.J., Wade, P.A., Vermaak, D., Kass, S.U., Landsberger, N., Strouboulis, J. and Wolffe, A.P. (1998) Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription. Nat. Genet., 19, 187-191.
-
(1998)
Nat. Genet.
, vol.19
, pp. 187-191
-
-
Jones, P.L.1
Veenstra, G.J.2
Wade, P.A.3
Vermaak, D.4
Kass, S.U.5
Landsberger, N.6
Strouboulis, J.7
Wolffe, A.P.8
-
2
-
-
0032574977
-
Transcriptional repression by the methyl-CpG binding protein MeCP2 involves a histone deacetylase complex
-
Nan, X., Ng, H.H., Johnson, C.A., Laherty, C.D., Turner, B.M., Eisenman, R.N. and Bird, A. (1998) Transcriptional repression by the methyl-CpG binding protein MeCP2 involves a histone deacetylase complex. Nature, 393, 386-389.
-
(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
-
3
-
-
0038412822
-
The methyl-CpG binding protein MeCP2 links DNA methylation to histone methylation
-
Fuks, F., Hurd, P.J., Deplus, R. and Kouzarides, T. (2003) The methyl-CpG binding protein MeCP2 links DNA methylation to histone methylation. Nucleic Acids Res., 31, 2305-2312.
-
(2003)
Nucleic Acids Res.
, vol.31
, pp. 2305-2312
-
-
Fuks, F.1
Hurd, P.J.2
Deplus, R.3
Kouzarides, T.4
-
4
-
-
33847282970
-
Interaction between chromatic proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation
-
Nan, X., Hou, J., Maclean, A., Nasir, J., Lafuente, M.J., Shu, X., Kriaucionis, S. and Bird, A. (2007) Interaction between chromatic proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation. Proc. Natl Acad. Sci. USA, 104, 2709-2714.
-
(2007)
Proc. Natl Acad. Sci. USA
, vol.104
, pp. 2709-2714
-
-
Nan, X.1
Hou, J.2
Maclean, A.3
Nasir, J.4
Lafuente, M.J.5
Shu, X.6
Kriaucionis, S.7
Bird, A.8
-
5
-
-
45849105557
-
MeCP2, a key contributor to neurological disease, activates and represses transcription
-
Chahrour, M., Jung, S.Y., Shaw, C., Zhou, X., Wong, S.T., Qin, J. and Zoghbi, H.Y. (2008) MeCP2, a key contributor to neurological disease, activates and represses transcription. Science, 320, 1224-1229.
-
(2008)
Science
, vol.320
, pp. 1224-1229
-
-
Chahrour, M.1
Jung, S.Y.2
Shaw, C.3
Zhou, X.4
Wong, S.T.5
Qin, J.6
Zoghbi, H.Y.7
-
6
-
-
0642336945
-
MeCP2 repression goes nonglobal
-
Klose, R. and Bird, A. (2003) MeCP2 repression goes nonglobal. Science, 302, 793-795.
-
(2003)
Science
, vol.302
, pp. 793-795
-
-
Klose, R.1
Bird, A.2
-
7
-
-
35648978121
-
The story of Rett syndrome: from clinic to neurobiology
-
Chahrour, M. and Zoghbi, H.Y. (2007) The story of Rett syndrome: from clinic to neurobiology. Neuron, 56, 422-437.
-
(2007)
Neuron
, vol.56
, pp. 422-437
-
-
Chahrour, M.1
Zoghbi, H.Y.2
-
8
-
-
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, L.R., Gecz, J. et al. (2005) Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males. Am. J. Hum. Genet, 73, 422-453.
-
(2005)
Am. J. Hum. Genet
, vol.73
, pp. 422-453
-
-
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
-
9
-
-
58149340280
-
Mouse models of Rett syndrome: from behavioural phenotyping to preclinical evaluation of new therapeutic approaches
-
Ricceri, L., De Filippis, B. and Laviola, G. (2008) Mouse models of Rett syndrome: from behavioural phenotyping to preclinical evaluation of new therapeutic approaches. Behav. Pharmacol., 19, 501-517.
-
(2008)
Behav. Pharmacol.
, vol.19
, pp. 501-517
-
-
Ricceri, L.1
De Filippis, B.2
Laviola, G.3
-
10
-
-
60749102039
-
Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology
-
Ballas, N., Lioy, D.T., Grunseich, C. and Mandel, G. (2009) Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology. Nat. Neurosci., 12, 311-317.
-
(2009)
Nat. Neurosci.
, vol.12
, pp. 311-317
-
-
Ballas, N.1
Lioy, D.T.2
Grunseich, C.3
Mandel, G.4
-
11
-
-
65549144456
-
Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions
-
Maezawa, I., Swanberg, S., Harvey, D., LaSalle, J.M. and Jin, L.W. (2009) Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions. J. Neurosci., 29, 5051-5061.
-
(2009)
J. Neurosci.
, vol.29
, pp. 5051-5061
-
-
Maezawa, I.1
Swanberg, S.2
Harvey, D.3
LaSalle, J.M.4
Jin, L.W.5
-
12
-
-
13244255460
-
CLOE: identification of putative functional relationships among genes by comparison of expression profiles between two species
-
Pellegrino, M., Provero, P., Silengo, L. and Di Cunto, F. (2004) CLOE: identification of putative functional relationships among genes by comparison of expression profiles between two species. BMC Bioinformatics, 5, 179.
-
(2004)
BMC Bioinformatics
, vol.5
, pp. 179
-
-
Pellegrino, M.1
Provero, P.2
Silengo, L.3
Di Cunto, F.4
-
13
-
-
41849139980
-
Functional annotation and identification of candidate genes by computational analysis of normal tissue gene expression data
-
Ala, U., Piro, R.M., Grassi, E., Damasco, C., Silengo, L., Oti, M., Provero, P. and Di Cunto, F. (2008) Functional annotation and identification of candidate genes by computational analysis of normal tissue gene expression data. PLoS Comput. Biol., 4, e1000043.
-
(2008)
PLoS Comput. Biol.
, vol.4
-
-
Ala, U.1
Piro, R.M.2
Grassi, E.3
Damasco, C.4
Silengo, L.5
Oti, M.6
Provero, P.7
Di Cunto, F.8
-
14
-
-
0032819331
-
Unlocking the mechanisms of transcription factor YY1: are chromatin modifying enzymes the key?
-
Thomas, M.J. and Seto, E. (1999) Unlocking the mechanisms of transcription factor YY1: are chromatin modifying enzymes the key? Gene, 236, 197-208.
-
(1999)
Gene
, vol.236
, pp. 197-208
-
-
Thomas, M.J.1
Seto, E.2
-
15
-
-
33845898866
-
Polycomb recruitment to DNA in vivo by the YY1 REPO domain
-
Wilkinson, F.H., Park, K. and Atchison, M.L. (2006) Polycomb recruitment to DNA in vivo by the YY1 REPO domain. Proc. Natl Acad. Sci. USA, 103, 19296-19301.
-
(2006)
Proc. Natl Acad. Sci. USA
, vol.103
, pp. 19296-19301
-
-
Wilkinson, F.H.1
Park, K.2
Atchison, M.L.3
-
16
-
-
0034905085
-
Regulation of transcription factor YY1 by acetylation and deacetylation
-
Yao, Y.L., Yang, W.M. and Seto, E. (2001) Regulation of transcription factor YY1 by acetylation and deacetylation. Mol. Cell. Biol., 21, 5979-5991.
-
(2001)
Mol. Cell. Biol.
, vol.21
, pp. 5979-5991
-
-
Yao, Y.L.1
Yang, W.M.2
Seto, E.3
-
17
-
-
1642377315
-
Molecular basis of fascioscapulohumeral muscular dystrophy
-
Tupler, R. and Gabellini, D. (2004) Molecular basis of fascioscapulohumeral muscular dystrophy. Cell. Mol. Life. Sci, 61, 557-566.
-
(2004)
Cell. Mol. Life. Sci
, vol.61
, pp. 557-566
-
-
Tupler, R.1
Gabellini, D.2
-
18
-
-
0037047439
-
Inappropriate gene activation in FSHD: a repressor complex binds a chromosomal repeat deleted in dystrophic muscle
-
Gabellini, D., Green, M.R. and Tupler, R. (2002) Inappropriate gene activation in FSHD: a repressor complex binds a chromosomal repeat deleted in dystrophic muscle. Cell, 110, 339-348.
-
(2002)
Cell
, vol.110
, pp. 339-348
-
-
Gabellini, D.1
Green, M.R.2
Tupler, R.3
-
19
-
-
33745479882
-
Gene expression analysis exposes mitochondrial abnormalities in a mouse model of Rett syndrome
-
Kriaucionis, S., Paterson, A., Curtis, J., Guy, J., Macleod, N. and Bird, A. (2006) Gene expression analysis exposes mitochondrial abnormalities in a mouse model of Rett syndrome. Mol. Cell Biol., 26, 5033-5042.
-
(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
-
20
-
-
0037101849
-
Infantile hypotonia as a presentation of Rett syndrome
-
Heilstedt, H.A., Shahbazian, M.D. and Lee, B. (2002) Infantile hypotonia as a presentation of Rett syndrome. Am. J. Med. Genet., 111, 238-242.
-
(2002)
Am. J. Med. Genet.
, vol.111
, pp. 238-242
-
-
Heilstedt, H.A.1
Shahbazian, M.D.2
Lee, B.3
-
21
-
-
65349122404
-
Widespread changes in dendritic and axonal morphology in Mecp2-mutant mouse models of Rett syndrome: evidence for disruption of neuronal networks
-
Belichenko, P.V., Wright, E.E., Belichenko, N.P., Masliah, E., Li, H.H., Mobley, W.C. and Francke, U. (2009) Widespread changes in dendritic and axonal morphology in Mecp2-mutant mouse models of Rett syndrome: evidence for disruption of neuronal networks. J. Comp. Neurol., 514, 240-258.
-
(2009)
J. Comp. Neurol.
, vol.514
, pp. 240-258
-
-
Belichenko, P.V.1
Wright, E.E.2
Belichenko, N.P.3
Masliah, E.4
Li, H.H.5
Mobley, W.C.6
Francke, U.7
-
22
-
-
0034702878
-
Expression and sequence analysis of the mouse adenine nucleotide translocase 1 and 2 genes
-
Levy, S.E., Chen, Y.S., Graham, B.H. and Wallace, D.C. (2000) Expression and sequence analysis of the mouse adenine nucleotide translocase 1 and 2 genes. Gene, 254, 57-66.
-
(2000)
Gene
, vol.254
, pp. 57-66
-
-
Levy, S.E.1
Chen, Y.S.2
Graham, B.H.3
Wallace, D.C.4
-
23
-
-
61449248092
-
Differential CpG island methylation of murine adenine nucleotide translocase genes
-
Brower, J.V., Lim, C.H., Han, C., Hankowski, K.E., Hamazaki, T. and Terada, N. (2009) Differential CpG island methylation of murine adenine nucleotide translocase genes. Biochim. Biophys. Acta, 1789, 198-203.
-
(2009)
Biochim. Biophys. Acta
, vol.1789
, pp. 198-203
-
-
Brower, J.V.1
Lim, C.H.2
Han, C.3
Hankowski, K.E.4
Hamazaki, T.5
Terada, N.6
-
24
-
-
33847266846
-
Reversal of neurological defects in a mouse model of Rett syndrome
-
Guy, J., Gan, J., Selfridge, J., Cobb, S. and Bird, A. (2007) Reversal of neurological defects in a mouse model of Rett syndrome. Science, 315, 1143-1147.
-
(2007)
Science
, vol.315
, pp. 1143-1147
-
-
Guy, J.1
Gan, J.2
Selfridge, J.3
Cobb, S.4
Bird, A.5
-
25
-
-
56349131682
-
Yin Yang 1 expression in the adult rodent brain
-
Rylski, M., Amborska, R., Zybura, K., Konopacki, F.A., Wilczynski, G.M. and Kaczmarek, L. (2008) Yin Yang 1 expression in the adult rodent brain. Neurochem. Res., 33, 2556-2564.
-
(2008)
Neurochem. Res.
, vol.33
, pp. 2556-2564
-
-
Rylski, M.1
Amborska, R.2
Zybura, K.3
Konopacki, F.A.4
Wilczynski, G.M.5
Kaczmarek, L.6
-
26
-
-
34447262102
-
The transcription factor Yin Yang 1 is essential for oligodendrocyte progenitor differentiation
-
He, Y., Dupree, J., Wang, J., Sandoval, J., Li, J., Liu, H., Shi, Y., Nave, K.A. and Casaccia-Bonnefil, P. (2007) The transcription factor Yin Yang 1 is essential for oligodendrocyte progenitor differentiation. Neuron, 55, 217-230.
-
(2007)
Neuron
, vol.55
, pp. 217-230
-
-
He, Y.1
Dupree, J.2
Wang, J.3
Sandoval, J.4
Li, J.5
Liu, H.6
Shi, Y.7
Nave, K.A.8
Casaccia-Bonnefil, P.9
-
27
-
-
8744240156
-
FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients
-
Rijkers, T., Deidda, G., van Koningsbruggen, S., van Geel, M., Lemmers, R.J., van Deutekom, J.C., Figlewicz, D., Hewitt, J.E., Padberg, G.W., Frants, R.R. and van der Maarel, S.M. (2004) FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients. J. Med. Genet., 41, 826-836.
-
(2004)
J. Med. Genet.
, vol.41
, pp. 826-836
-
-
Rijkers, T.1
Deidda, G.2
van Koningsbruggen, S.3
van Geel, M.4
Lemmers, R.J.5
van Deutekom, J.C.6
Figlewicz, D.7
Hewitt, J.E.8
Padberg, G.W.9
Frants, R.R.10
van der Maarel, S.M.11
-
28
-
-
0034327571
-
Functional consequences of Rett syndrome mutations on human MeCP2
-
Yusufzai, T.M. and Wolffe, A.P. (2000) Functional consequences of Rett syndrome mutations on human MeCP2. Nucleic Acids Res., 28, 4172-4179.
-
(2000)
Nucleic Acids Res.
, vol.28
, pp. 4172-4179
-
-
Yusufzai, T.M.1
Wolffe, A.P.2
-
29
-
-
34447536953
-
Intrinsic disorder and autonomous domain function in the multifunctional nuclear protein
-
Adams, V.H., McBryant, S.J., Wade, P.A., Woodcock, C.L. and Hansen, J.C. (2007) Intrinsic disorder and autonomous domain function in the multifunctional nuclear protein, MeCP2. J. Biol. Chem., 282, 15057-15064.
-
(2007)
MeCP2. J. Biol. Chem.
, vol.282
, pp. 15057-15064
-
-
Adams, V.H.1
McBryant, S.J.2
Wade, P.A.3
Woodcock, C.L.4
Hansen, J.C.5
-
30
-
-
34948908780
-
MeCP2-chromatin interactions include the formation of chromatosome-like structures and are altered in mutations causing Rett syndrome
-
Nikitina, T., Ghosh, R.P., Horowitz-Scherer, R.A., Hansen, J.C., Grigoryev, S.A. and Woodcock, C.L. (2007) MeCP2-chromatin interactions include the formation of chromatosome-like structures and are altered in mutations causing Rett syndrome. J. Biol. Chem., 282, 28237-28345.
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 28237-28345
-
-
Nikitina, T.1
Ghosh, R.P.2
Horowitz-Scherer, R.A.3
Hansen, J.C.4
Grigoryev, S.A.5
Woodcock, C.L.6
-
31
-
-
27444433840
-
The adenine nucleotide translocase type 1 (ANT1): a new factor in mitochondrial disease
-
Sharer, J.D. (2005) The adenine nucleotide translocase type 1 (ANT1): a new factor in mitochondrial disease. IUBMB Life, 57, 607-614.
-
(2005)
IUBMB Life
, vol.57
, pp. 607-614
-
-
Sharer, J.D.1
-
32
-
-
85058249156
-
A third locus predisposing to multiple deletions of mtDNA in autosomal dominant progressive external ophthalmoplegia
-
Kaukonen, J., Zeviani, M., Comi, G.P., Piscaglia, M.G., Peltonen, L. and Suomalainen, A. (1999) A third locus predisposing to multiple deletions of mtDNA in autosomal dominant progressive external ophthalmoplegia. Am. J. Hum. Genet., 65, 226-234.
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 226-234
-
-
Kaukonen, J.1
Zeviani, M.2
Comi, G.P.3
Piscaglia, M.G.4
Peltonen, L.5
Suomalainen, A.6
-
33
-
-
0034604506
-
Role of adenine nucleotide translocator 1 in mtDNA maintenance
-
Kaukonen, J., Juselius, J.K., Tiranti, V., Kyttala, A., Zeviani, M., Comi, G.P., Keranen, S., Peltonen, L. and Suomalainen, A. (2000) Role of adenine nucleotide translocator 1 in mtDNA maintenance. Science, 289, 782-785.
-
(2000)
Science
, vol.289
, pp. 782-785
-
-
Kaukonen, J.1
Juselius, J.K.2
Tiranti, V.3
Kyttala, A.4
Zeviani, M.5
Comi, G.P.6
Keranen, S.7
Peltonen, L.8
Suomalainen, A.9
-
34
-
-
0031011211
-
A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator
-
Graham, B.H., Waymire, K.G., Cottrell, B., Trounce, I.A., MacGregor, G.R. and Wallace, D.C. (1997) A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator. Nat. Genet., 16, 226-234.
-
(1997)
Nat. Genet.
, vol.16
, pp. 226-234
-
-
Graham, B.H.1
Waymire, K.G.2
Cottrell, B.3
Trounce, I.A.4
MacGregor, G.R.5
Wallace, D.C.6
-
35
-
-
0033611057
-
Adenine nucleotide translocase-1, a component of the permeability pore, can dominantly induce apoptosis
-
Bauer, M.K.A., Schubert, A., Rocks, O. and Grimm, S. (1999) Adenine nucleotide translocase-1, a component of the permeability pore, can dominantly induce apoptosis. J. Cell. Biol., 147, 1493-1501.
-
(1999)
J. Cell. Biol.
, vol.147
, pp. 1493-1501
-
-
Bauer, M.K.A.1
Schubert, A.2
Rocks, O.3
Grimm, S.4
-
36
-
-
33745715007
-
Facioscapulohumeral muscular dystrophy
-
Tawil, R. and Van Der Maarel, S.M. (2006) Facioscapulohumeral muscular dystrophy. Muscle Nerve, 34, 1-15.
-
(2006)
Muscle Nerve
, vol.34
, pp. 1-15
-
-
Tawil, R.1
Van Der Maarel, S.M.2
-
37
-
-
0029113034
-
The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arm of the acrocentric chromosomes
-
Lyle, R., Wright, T.J., Clark, I.N. and Hewitt, J.E. (1995) The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arm of the acrocentric chromosomes. Genomics, 28, 389-397.
-
(1995)
Genomics
, vol.28
, pp. 389-397
-
-
Lyle, R.1
Wright, T.J.2
Clark, I.N.3
Hewitt, J.E.4
-
38
-
-
0035094767
-
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome
-
Guy, J., Hendrich, B., Holmes, M., Martin, J.E. and Bird, A. (2001) A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome. Nat. Genet., 27, 322-326.
-
(2001)
Nat. Genet.
, vol.27
, pp. 322-326
-
-
Guy, J.1
Hendrich, B.2
Holmes, M.3
Martin, J.E.4
Bird, A.5
-
39
-
-
26444495179
-
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome
-
Mari, F., Azimonti, S., Bertani, I., Bolognese, F., Colombo, E., Caselli, R., Scala, E., Longo, I., Grosso, S., Pescucci, C. et al. (2005) CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome. Hum. Mol. Genet., 14, 1935-1946.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 1935-1946
-
-
Mari, F.1
Azimonti, S.2
Bertani, I.3
Bolognese, F.4
Colombo, E.5
Caselli, R.6
Scala, E.7
Longo, I.8
Grosso, S.9
Pescucci, C.10
-
40
-
-
33845988053
-
Functional consequences of mutations in CDKL5, an X-linked gene involved in infantile spasms and mental retardation
-
Bertani, I., Rusconi, L., Bolognese, F., Forlani, G., Conca, B., De Monte, L., Badaracco, G., Landsberger, N. and Kilstrup-Nielsen, C. (2006) Functional consequences of mutations in CDKL5, an X-linked gene involved in infantile spasms and mental retardation. J. Biol. Chem., 281, 32048-32056.
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 32048-32056
-
-
Bertani, I.1
Rusconi, L.2
Bolognese, F.3
Forlani, G.4
Conca, B.5
De Monte, L.6
Badaracco, G.7
Landsberger, N.8
Kilstrup-Nielsen, C.9
-
41
-
-
0036856355
-
MethPrimer: designing primers for methylation PCRs
-
Li, L.C. and Dahiya, R. (2002) MethPrimer: designing primers for methylation PCRs. Bioinformatics, 18, 1427-1431.
-
(2002)
Bioinformatics
, vol.18
, pp. 1427-1431
-
-
Li, L.C.1
Dahiya, R.2
|