-
1
-
-
78751590899
-
Silencing chromatin: Comparing modes and mechanisms
-
Beisel C., Paro R., Silencing chromatin: comparing modes and mechanisms Nature Reviews Genetics 2011 12 2 123 135
-
(2011)
Nature Reviews Genetics
, vol.12
, Issue.2
, pp. 123-135
-
-
Beisel, C.1
Paro, R.2
-
3
-
-
79956330964
-
CpG islands and the regulation of transcription
-
Deaton A. M., Bird A., CpG islands and the regulation of transcription Genes and Development 2011 25 10 1010 1022
-
(2011)
Genes and Development
, vol.25
, Issue.10
, pp. 1010-1022
-
-
Deaton, A.M.1
Bird, A.2
-
4
-
-
34247557054
-
The function of the epigenome in cell reprogramming
-
DOI 10.1007/s00018-007-6420-8
-
Lanzuolo C., Orlando V., The function of the epigenome in cell reprogramming Cellular and Molecular Life Sciences 2007 64 9 1043 1062 (Pubitemid 46684544)
-
(2007)
Cellular and Molecular Life Sciences
, vol.64
, Issue.9
, pp. 1043-1062
-
-
Lanzuolo, C.1
Orlando, V.2
-
5
-
-
79960622503
-
Biogenesis and function of nuclear bodies
-
Mao Y. S., Zhang B., Spector D. L., Biogenesis and function of nuclear bodies Trends in Genetics 2011 27 8 295 306
-
(2011)
Trends in Genetics
, vol.27
, Issue.8
, pp. 295-306
-
-
Mao, Y.S.1
Zhang, B.2
Spector, D.L.3
-
6
-
-
80053144962
-
A decade of exploring the cancer epigenomebiological and translational implications
-
Baylin S. B., Jones P. A., A decade of exploring the cancer epigenomebiological and translational implications Nature Reviews Cancer 2011 11 726 773
-
(2011)
Nature Reviews Cancer
, vol.11
, pp. 726-773
-
-
Baylin, S.B.1
Jones, P.A.2
-
7
-
-
35848951163
-
Covalent modifications of histones during development and disease pathogenesis
-
DOI 10.1038/nsmb1337, PII NSMB1337
-
Bhaumik S. R., Smith E., Shilatifard A., Covalent modifications of histones during development and disease pathogenesis Nature Structural and Molecular Biology 2007 14 11 1008 1016 (Pubitemid 350060343)
-
(2007)
Nature Structural and Molecular Biology
, vol.14
, Issue.11
, pp. 1008-1016
-
-
Bhaumik, S.R.1
Smith, E.2
Shilatifard, A.3
-
8
-
-
0032992224
-
DNA methylation represses transcription in vivo
-
DOI 10.1038/9727
-
Siegfried Z., Eden S., Mendelsohn M., Feng X., Tsuberi B. Z., Cedar H., DNA methylation represses transcription in vivo Nature Genetics 1999 22 2 203 206 (Pubitemid 29264820)
-
(1999)
Nature Genetics
, vol.22
, Issue.2
, pp. 203-206
-
-
Siegfried, Z.1
Eden, S.2
Mendelsohn, M.3
Feng, X.4
Tsuberi, B.-Z.5
Cedar, H.6
-
9
-
-
33646471380
-
DNA methylation supports intrinsic epigenetic memory in mammalian cells
-
ARTICLE E65
-
Feng Y. Q., Desprat R., Fu H., Olivier E., Lin C. M., Lobell A., Gowda S. N., Aladjem M. I., Bouhassira E. E., DNA methylation supports intrinsic epigenetic memory in mammalian cells PLoS Genetics 2006 2 4, article e65
-
(2006)
PLoS Genetics
, vol.2
, Issue.4
-
-
Feng, Y.Q.1
Desprat, R.2
Fu, H.3
Olivier, E.4
Lin, C.M.5
Lobell, A.6
Gowda, S.N.7
Aladjem, M.I.8
Bouhassira, E.E.9
-
10
-
-
0022000776
-
A fraction of the mouse genome that is derived from islands of nonmethylated, CpG-rich DNA
-
Bird A., Taggart M., Frommer M., Miller O. J., Macleod D., A fraction of the mouse genome that is derived from islands of nonmethylated, CpG-rich DNA Cell 1985 40 1 91 99 (Pubitemid 15169310)
-
(1985)
Cell
, vol.40
, Issue.1
, pp. 91-99
-
-
Bird, A.1
Taggart, M.2
Frommer, M.3
-
11
-
-
67349255210
-
CpG islandsa rough guide
-
Illingworth R. S., Bird A. P., CpG islandsa rough guide FEBS Letters 2009 583 11 1713 1720
-
(2009)
FEBS Letters
, vol.583
, Issue.11
, pp. 1713-1720
-
-
Illingworth, R.S.1
Bird, A.P.2
-
12
-
-
78049419464
-
Orphan CpG Islands Identify numerous conserved promoters in the mammalian genome
-
ARTICLE E1001134
-
Illingworth R. S., Gruenewald-Schneider U., Webb S., Kerr A. R. W., James K. D., Turner D. J., Smith C., Harrison D. J., Andrews R., Bird A. P., Orphan CpG Islands Identify numerous conserved promoters in the mammalian genome PLoS Genetics 2010 6 9, article e1001134
-
(2010)
PLoS Genetics
, vol.6
, Issue.9
-
-
Illingworth, R.S.1
Gruenewald-Schneider, U.2
Webb, S.3
Kerr, A.R.W.4
James, K.D.5
Turner, D.J.6
Smith, C.7
Harrison, D.J.8
Andrews, R.9
Bird, A.P.10
-
13
-
-
66149123748
-
The nuclear DNA base 5-hydroxymethylcytosine is present in purkinje neurons and the brain
-
Kriaucionis S., Heintz N., The nuclear DNA base 5-hydroxymethylcytosine is present in purkinje neurons and the brain Science 2009 324 5929 929 930
-
(2009)
Science
, vol.324
, Issue.5929
, pp. 929-930
-
-
Kriaucionis, S.1
Heintz, N.2
-
14
-
-
66149146320
-
Conversion of 5-methylcytosine to 5-hydroxymethylcytosine in mammalian DNA by MLL partner TET1
-
Tahiliani M., Koh K. P., Shen Y., Pastor W. A., Bandukwala H., Brudno Y., Agarwal S., Iyer L. M., Liu D. R., Aravind L., Rao A., Conversion of 5-methylcytosine to 5-hydroxymethylcytosine in mammalian DNA by MLL partner TET1 Science 2009 324 5929 930 935
-
(2009)
Science
, vol.324
, Issue.5929
, pp. 930-935
-
-
Tahiliani, M.1
Koh, K.P.2
Shen, Y.3
Pastor, W.A.4
Bandukwala, H.5
Brudno, Y.6
Agarwal, S.7
Iyer, L.M.8
Liu, D.R.9
Aravind, L.10
Rao, A.11
-
15
-
-
77956189495
-
Role of tet proteins in 5mC to 5hmC conversion, ES-cell self-renewal and inner cell mass specification
-
Ito S., DAlessio A. C., Taranova O. V., Hong K., Sowers L. C., Zhang Y., Role of tet proteins in 5mC to 5hmC conversion, ES-cell self-renewal and inner cell mass specification Nature 2010 466 7310 1129 1133
-
(2010)
Nature
, vol.466
, Issue.7310
, pp. 1129-1133
-
-
Ito, S.1
Dalessio, A.C.2
Taranova, O.V.3
Hong, K.4
Sowers, L.C.5
Zhang, Y.6
-
16
-
-
84863707654
-
The involvement of 5-hydroxymethylcytosine in active DNA demethylation in mice
-
Zhang P., Su L., Wang Z., Zhang S., Guan J., The involvement of 5-hydroxymethylcytosine in active DNA demethylation in mice Biology of Reproduction 2012 86 4 104
-
(2012)
Biology of Reproduction
, vol.86
, Issue.4
, pp. 104
-
-
Zhang, P.1
Su, L.2
Wang, Z.3
Zhang, S.4
Guan, J.5
-
17
-
-
59849126153
-
Histone modifications dictate specific biological readouts
-
Munshi A., Shafi G., Aliya N., Jyothy A., Histone modifications dictate specific biological readouts Journal of Genetics and Genomics 2009 36 2 75 88
-
(2009)
Journal of Genetics and Genomics
, vol.36
, Issue.2
, pp. 75-88
-
-
Munshi, A.1
Shafi, G.2
Aliya, N.3
Jyothy, A.4
-
18
-
-
34247172850
-
Histone modifications in response to DNA damage
-
DOI 10.1016/j.mrfmmm.2006.09.009, PII S0027510707000280, Chromatin: Repair, Remodeling and Regulation
-
Altaf M., Saksouk N., Cté J., Histone modifications in response to DNA damage Mutation Research 2007 618 1-2 81 90 (Pubitemid 46584693)
-
(2007)
Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
, vol.618
, Issue.1-2
, pp. 81-90
-
-
Altaf, M.1
Saksouk, N.2
Cote, J.3
-
19
-
-
77954386433
-
Accessibility of the Drosophila genome discriminates PcG repression, H4K16 acetylation and replication timing
-
Bell O., Schwaiger M., Oakeley E. J., Lienert F., Beisel C., Stadler M. B., Schbeler D., Accessibility of the Drosophila genome discriminates PcG repression, H4K16 acetylation and replication timing Nature Structural and Molecular Biology 2010 17 7 894 900
-
(2010)
Nature Structural and Molecular Biology
, vol.17
, Issue.7
, pp. 894-900
-
-
Bell, O.1
Schwaiger, M.2
Oakeley, E.J.3
Lienert, F.4
Beisel, C.5
Stadler, M.B.6
Schbeler, D.7
-
20
-
-
19944430797
-
Genomic maps and comparative analysis of histone modifications in human and mouse
-
DOI 10.1016/j.cell.2005.01.001, PII S0092867405000395
-
Bernstein B. E., Kamal M., Lindblad-Toh K., Bekiranov S., Bailey D. K., Huebert D. J., McMahon S., Karlsson E. K., Kulbokas E. J., Gingeras T. R., Schreiber S. L., Lander E. S., Genomic maps and comparative analysis of histone modifications in human and mouse Cell 2005 120 2 169 181 (Pubitemid 40174761)
-
(2005)
Cell
, vol.120
, Issue.2
, pp. 169-181
-
-
Bernstein, B.E.1
Kamal, M.2
Lindblad-Toh, K.3
Bekiranov, S.4
Bailey, D.K.5
Huebert, D.J.6
McMahon, S.7
Karlsson, E.K.8
Kulbokas III, E.J.9
Gingeras, T.R.10
Schreiber, S.L.11
Lander, E.S.12
-
21
-
-
79551581102
-
Chromatin signatures of the Drosophila replication program
-
Eaton M. L., Prinz J. A., MacAlpine H. K., Tretyakov G., Kharchenko P. V., MacAlpine D. M., Chromatin signatures of the Drosophila replication program Genome Research 2011 21 2 164 174
-
(2011)
Genome Research
, vol.21
, Issue.2
, pp. 164-174
-
-
Eaton, M.L.1
Prinz, J.A.2
MacAlpine, H.K.3
Tretyakov, G.4
Kharchenko, P.V.5
MacAlpine, D.M.6
-
22
-
-
77957776228
-
Systematic protein location mapping reveals five principal chromatin types in Drosophila cells
-
Filion G. J., van Bemmel J. G., Braunschweig U., Talhout W., Kind J., Systematic protein location mapping reveals five principal chromatin types in Drosophila cells Cell 2010 143 212 224
-
(2010)
Cell
, vol.143
, pp. 212-224
-
-
Filion, G.J.1
Van Bemmel, J.G.2
Braunschweig, U.3
Talhout, W.4
Kind, J.5
-
23
-
-
79961083402
-
Histone H4 lysine 16 hypoacetylation is associated with defective DNA repair and premature senescence in Zmpste24-deficient mice
-
Krishnan V., Chow M. Z. Y., Wang Z., Zhang L., Liu B., Liu X., Zhou Z., Histone H4 lysine 16 hypoacetylation is associated with defective DNA repair and premature senescence in Zmpste24-deficient mice Proceedings of the National Academy of Sciences of the United States of America 2011 108 30 12325 12330
-
(2011)
Proceedings of the National Academy of Sciences of the United States of America
, vol.108
, Issue.30
, pp. 12325-12330
-
-
Krishnan, V.1
Chow, M.Z.Y.2
Wang, Z.3
Zhang, L.4
Liu, B.5
Liu, X.6
Zhou, Z.7
-
24
-
-
2642570305
-
The histone modification pattern of active genes revealed through genome-wide chromatin analysis of a higher eukaryote
-
DOI 10.1101/gad.1198204
-
Schbeler D., MacAlpine D. M., Scalzo D., Wirbelauer C., Kooperberg C., Van Leeuwen F., Gottschling D. E., O'Neill L. P., Turner B. M., Delrow J., Bell S. P., Groudine M., The histone modification pattern of active genes revealed through genome-wide chromatin analysis of a higher eukaryote Genes and Development 2004 18 11 1263 1271 (Pubitemid 38720594)
-
(2004)
Genes and Development
, vol.18
, Issue.11
, pp. 1263-1271
-
-
Schubeler, D.1
MacAlpine, D.M.2
Scalzo, D.3
Wirbelauer, C.4
Kooperberg, C.5
Van Leeuwen, F.6
Gottschling, D.E.7
O'Neill, L.P.8
Turner, B.M.9
Delrow, J.10
Bell, S.P.11
Groudine, M.12
-
25
-
-
27144544622
-
Assembly of variant histones into chromatin
-
DOI 10.1146/annurev.cellbio.21.012704.133518
-
Henikoff S., Ahmad K., Assembly of variant histones into chromatin Annual Review of Cell and Developmental Biology 2005 21 133 153 (Pubitemid 41740630)
-
(2005)
Annual Review of Cell and Developmental Biology
, vol.21
, pp. 133-153
-
-
Henikoff, S.1
Ahmad, K.2
-
26
-
-
81855212627
-
Trithorax group proteins: Switching genes on and keeping them active
-
Schuettengruber B., Martinez A. M., Iovino N., Cavalli G., Trithorax group proteins: switching genes on and keeping them active Nature Reviews Molecular Cell Biology 2011 12 799 814
-
(2011)
Nature Reviews Molecular Cell Biology
, vol.12
, pp. 799-814
-
-
Schuettengruber, B.1
Martinez, A.M.2
Iovino, N.3
Cavalli, G.4
-
27
-
-
80455143728
-
The complex transcription regulatory landscape of our genome: Control in three dimensions
-
Splinter E., de Laat W., The complex transcription regulatory landscape of our genome: control in three dimensions EMBO Journal 2011 30 4345 4355
-
(2011)
EMBO Journal
, vol.30
, pp. 4345-4355
-
-
Splinter, E.1
De Laat, W.2
-
29
-
-
34249307315
-
Nuclear organization of the genome and the potential for gene regulation
-
DOI 10.1038/nature05916, PII NATURE05916
-
Fraser P., Bickmore W., Nuclear organization of the genome and the potential for gene regulation Nature 2007 447 7143 413 417 (Pubitemid 46816747)
-
(2007)
Nature
, vol.447
, Issue.7143
, pp. 413-417
-
-
Fraser, P.1
Bickmore, W.2
-
30
-
-
33846283384
-
Dynamic genome architecture in the nuclear space: Regulation of gene expression in three dimensions
-
DOI 10.1038/nrg2041, PII NRG2041
-
Lanctt C., Cheutin T., Cremer M., Cavalli G., Cremer T., Dynamic genome architecture in the nuclear space: regulation of gene expression in three dimensions Nature Reviews Genetics 2007 8 2 104 115 (Pubitemid 46122840)
-
(2007)
Nature Reviews Genetics
, vol.8
, Issue.2
, pp. 104-115
-
-
Lanctot, C.1
Cheutin, T.2
Cremer, M.3
Cavalli, G.4
Cremer, T.5
-
31
-
-
35549011494
-
Mobility and immobility of chromatin in transcription and genome stability
-
DOI 10.1016/j.gde.2007.08.004, PII S0959437X07001554, Differentiation and Gene Regulation
-
Soutoglou E., Misteli T., Mobility and immobility of chromatin in transcription and genome stability Current Opinion in Genetics and Development 2007 17 5 435 442 (Pubitemid 350016896)
-
(2007)
Current Opinion in Genetics and Development
, vol.17
, Issue.5
, pp. 435-442
-
-
Soutoglou, E.1
Misteli, T.2
-
33
-
-
33745151459
-
A polycomb group protein complex with sequence-specific DNA-binding and selective methyl-lysine-binding activities
-
Klymenko T., Papp B., Fischle W., Kcher T., Schelder M., Fritsch C., Wild B., Wilm M., Mller J., A polycomb group protein complex with sequence-specific DNA-binding and selective methyl-lysine-binding activities Genes and Development 2006 20 9 1110 1122
-
(2006)
Genes and Development
, vol.20
, Issue.9
, pp. 1110-1122
-
-
Klymenko, T.1
Papp, B.2
Fischle, W.3
Kcher, T.4
Schelder, M.5
Fritsch, C.6
Wild, B.7
Wilm, M.8
Mller, J.9
-
34
-
-
77952429798
-
Histone H2A deubiquitinase activity of the Polycomb repressive complex PR-DUB
-
Scheuermann J. C., de Ayala Alonso A. G., Oktaba K., Ly-Hartig N., McGinty R. K., Fraterman S., Wilm M., Muir T. W., Mller J., Histone H2A deubiquitinase activity of the Polycomb repressive complex PR-DUB Nature 2010 465 7295 243 247
-
(2010)
Nature
, vol.465
, Issue.7295
, pp. 243-247
-
-
Scheuermann, J.C.1
De Ayala Alonso, A.G.2
Oktaba, K.3
Ly-Hartig, N.4
McGinty, R.K.5
Fraterman, S.6
Wilm, M.7
Muir, T.W.8
Mller, J.9
-
35
-
-
0036830642
-
Role of histone H3 lysine 27 methylation in polycomb-group silencing
-
DOI 10.1126/science.1076997
-
Cao R., Wang L., Wang H., Xia L., Erdjument-Bromage H., Tempst P., Jones R. S., Zhang Y., Role of histone H3 lysine 27 methylation in polycomb-group silencing Science 2002 298 5595 1039 1043 (Pubitemid 35247314)
-
(2002)
Science
, vol.298
, Issue.5595
, pp. 1039-1043
-
-
Cao, R.1
Wang, L.2
Wang, H.3
Xia, L.4
Erdjument-Bromage, H.5
Tempst, P.6
Jones, R.S.7
Zhang, Y.8
-
36
-
-
0037131523
-
Drosophila enhancer of Zeste/ESC complexes have a histone H3 methyltransferase activity that marks chromosomal Polycomb sites
-
DOI 10.1016/S0092-8674(02)00975-3
-
Czermin B., Melfi R., McCabe D., Seitz V., Imhof A., Pirrotta V., Drosophila enhancer of Zeste/ESC complexes have a histone H3 methyltransferase activity that marks chromosomal Polycomb sites Cell 2002 111 2 185 196 (Pubitemid 35292439)
-
(2002)
Cell
, vol.111
, Issue.2
, pp. 185-196
-
-
Czermin, B.1
Melfi, R.2
McCabe, D.3
Seitz, V.4
Imhof, A.5
Pirrotta, V.6
-
37
-
-
0037111831
-
Histone methyltransferase activity associated with a human multiprotein complex containing the enhancer of zeste protein
-
DOI 10.1101/gad.1035902
-
Kuzmichev A., Nishioka K., Erdjument-Bromage H., Tempst P., Reinberg D., Histone methyltransferase activity associated with a human multiprotein complex containing the enhancer of zeste protein Genes and Development 2002 16 22 2893 2905 (Pubitemid 35334738)
-
(2002)
Genes and Development
, vol.16
, Issue.22
, pp. 2893-2905
-
-
Kuzmichev, A.1
Nishioka, K.2
Erdjument-Bromage, H.3
Tempst, P.4
Reinberg, D.5
-
38
-
-
18644383738
-
Histone methyltransferase activity of a Drosophila Polycomb group repressor complex
-
DOI 10.1016/S0092-8674(02)00976-5
-
Mller J., Hart C. M., Francis N. J., Vargas M. L., Sengupta A., Wild B., Miller E. L., O'Connor M. B., Kingston R. E., Simon J. A., Histone methyltransferase activity of a Drosophila Polycomb group repressor complex Cell 2002 111 2 197 208 (Pubitemid 35292440)
-
(2002)
Cell
, vol.111
, Issue.2
, pp. 197-208
-
-
Muller, J.1
Hart, C.M.2
Francis, N.J.3
Vargas, M.L.4
Sengupta, A.5
Wild, B.6
Miller, E.L.7
O'Connor, M.B.8
Kingston, R.E.9
Simon, J.A.10
-
39
-
-
7244234099
-
Role of histone H2A ubiquitination in Polycomb silencing
-
DOI 10.1038/nature02985
-
Wang H., Wang L., Erdjument-Bromage H., Vidal M., Tempst P., Jones R. S., Zhang Y., Role of histone H2A ubiquitination in Polycomb silencing Nature 2004 431 7010 873 878 (Pubitemid 39434086)
-
(2004)
Nature
, vol.431
, Issue.7010
, pp. 873-878
-
-
Wang, H.1
Wang, L.2
Erdjument-Bromage, H.3
Vidal, M.4
Tempst, P.5
Jones, R.S.6
Zhang, Y.7
-
40
-
-
55449105221
-
Genomewide analysis of PRC1 and PRC2 occupancy identifies two classes of bivalent domains
-
ARTICLE E1000242
-
Ku M., Koche R. P., Rheinbay E., Mendenhall E. M., Endoh M., Mikkelsen T. S., Presser A., Nusbaum C., Xie X., Chi A. S., Adli M., Kasif S., Ptaszek L. M., Cowan C. A., Lander E. S., Koseki H., Bernstein B. E., Genomewide analysis of PRC1 and PRC2 occupancy identifies two classes of bivalent domains PLoS Genetics 2008 4 10, article e1000242
-
(2008)
PLoS Genetics
, vol.4
, Issue.10
-
-
Ku, M.1
Koche, R.P.2
Rheinbay, E.3
Mendenhall, E.M.4
Endoh, M.5
Mikkelsen, T.S.6
Presser, A.7
Nusbaum, C.8
Xie, X.9
Chi, A.S.10
Adli, M.11
Kasif, S.12
Ptaszek, L.M.13
Cowan, C.A.14
Lander, E.S.15
Koseki, H.16
Bernstein, B.E.17
-
41
-
-
33746407708
-
Recruitment of PRC1 function at the initiation of X inactivation independent of PRC2 and silencing
-
DOI 10.1038/sj.emboj.7601187, PII 7601187
-
Schoeftner S., Sengupta A. K., Kubicek S., Mechtler K., Spahn L., Koseki H., Jenuwein T., Wutz A., Recruitment of PRC1 function at the initiation of X inactivation independent of PRC2 and silencing EMBO Journal 2006 25 13 3110 3122 (Pubitemid 44121103)
-
(2006)
EMBO Journal
, vol.25
, Issue.13
, pp. 3110-3122
-
-
Schoeftner, S.1
Sengupta, A.K.2
Kubicek, S.3
Mechtler, K.4
Spahn, L.5
Koseki, H.6
Jenuwein, T.7
Wutz, A.8
-
42
-
-
0037439634
-
Polycomb group gene silencing proteins are concentrated in the perichromatin compartment of the mammalian nucleus
-
DOI 10.1242/jcs.00225
-
Cmarko D., Verschure P. J., Otte A. P., van Driel R., Fakan S., Polycomb group gene silencing proteins are concentrated in the perichromatin compartment of the mammalian nucleus Journal of Cell Science 2003 116 2 335 343 (Pubitemid 36163874)
-
(2003)
Journal of Cell Science
, vol.116
, Issue.2
, pp. 335-343
-
-
Cmarko, D.1
Verschure, P.J.2
Otte, A.P.3
Van Driel, R.4
Fakan, S.5
-
43
-
-
78651514974
-
Polycomb-dependent regulatory contacts between distant hox loci in drosophila
-
Bantignies F., Roure V., Comet I., Leblanc B., Schuettengruber B., Bonnet J., Tixier V., Mas A., Cavalli G., Polycomb-dependent regulatory contacts between distant hox loci in drosophila Cell 2011 144 2 214 226
-
(2011)
Cell
, vol.144
, Issue.2
, pp. 214-226
-
-
Bantignies, F.1
Roure, V.2
Comet, I.3
Leblanc, B.4
Schuettengruber, B.5
Bonnet, J.6
Tixier, V.7
Mas, A.8
Cavalli, G.9
-
44
-
-
34848825691
-
Polycomb response elements mediate the formation of chromosome higher-order structures in the bithorax complex
-
DOI 10.1038/ncb1637, PII NCB1637
-
Lanzuolo C., Roure V., Dekker J., Bantignies F., Orlando V., Polycomb response elements mediate the formation of chromosome higher-order structures in the bithorax complex Nature Cell Biology 2007 9 10 1167 1174 (Pubitemid 47500493)
-
(2007)
Nature Cell Biology
, vol.9
, Issue.10
, pp. 1167-1174
-
-
Lanzuolo, C.1
Roure, V.2
Dekker, J.3
Bantignies, F.4
Orlando, V.5
-
45
-
-
33746472337
-
Probing long-distance regulatory interactions in the Drosophila melanogaster bithorax complex using Dam identification
-
DOI 10.1038/ng1833, PII NG1833
-
Cléard F., Moshkin Y., Karch F., Maeda R. K., Probing long-distance regulatory interactions in the Drosophila melanogaster bithorax complex using Dam identification Nature Genetics 2006 38 8 931 935 (Pubitemid 44141663)
-
(2006)
Nature Genetics
, vol.38
, Issue.8
, pp. 931-935
-
-
Cleard, F.1
Moshkin, Y.2
Karch, F.3
Maeda, R.K.4
-
46
-
-
84856747483
-
Three-dimensional folding and functional organization principles of the Drosophila genome
-
Sexton T., Yaffe E., Kenigsberg E., Bantignies F., Leblanc B., Three-dimensional folding and functional organization principles of the Drosophila genome Cell 2012 148 458 472
-
(2012)
Cell
, vol.148
, pp. 458-472
-
-
Sexton, T.1
Yaffe, E.2
Kenigsberg, E.3
Bantignies, F.4
Leblanc, B.5
-
47
-
-
77954814317
-
EZH2-dependent chromatin looping controls INK4a and INK4b, but not ARF, during human progenitor cell differentiation and cellular senescence
-
Kheradmand Kia S., Solaimani Kartalaei P., Farahbakhshian E., Pourfarzad F., von Lindern M., EZH2-dependent chromatin looping controls INK4a and INK4b, but not ARF, during human progenitor cell differentiation and cellular senescence Epigenetics Chromatin 2009 2 1 16
-
(2009)
Epigenetics Chromatin
, vol.2
, Issue.1
, pp. 16
-
-
Kheradmand Kia, S.1
Solaimani Kartalaei, P.2
Farahbakhshian, E.3
Pourfarzad, F.4
Von Lindern, M.5
-
48
-
-
80054110441
-
The dynamic architecture of Hox gene clusters
-
Noordermeer D., Leleu M., Splinter E., Rougemont J., De Laat W., The dynamic architecture of Hox gene clusters Science 2011 334 222 225
-
(2011)
Science
, vol.334
, pp. 222-225
-
-
Noordermeer, D.1
Leleu, M.2
Splinter, E.3
Rougemont, J.4
De Laat, W.5
-
49
-
-
84883798471
-
PcG proteins, DNA methylation, and gene repression by chromatin looping
-
Tiwari V. K., McGarvey K. M., Licchesi J. D. F., Ohm J. E., Herman J. G., Schbeler D., Baylin S. B., PcG proteins, DNA methylation, and gene repression by chromatin looping PLoS Biology 2008 6 12 2911 2927
-
(2008)
PLoS Biology
, vol.6
, Issue.12
, pp. 2911-2927
-
-
Tiwari, V.K.1
McGarvey, K.M.2
Licchesi, J.D.F.3
Ohm, J.E.4
Herman, J.G.5
Schbeler, D.6
Baylin, S.B.7
-
50
-
-
55549103314
-
A model for transmission of the H3K27me3 epigenetic mark
-
Hansen K. H., Bracken A. P., Pasini D., Dietrich N., Gehani S. S., Monrad A., Rappsilber J., Lerdrup M., Helin K., A model for transmission of the H3K27me3 epigenetic mark Nature Cell Biology 2008 10 11 1291 1300
-
(2008)
Nature Cell Biology
, vol.10
, Issue.11
, pp. 1291-1300
-
-
Hansen, K.H.1
Bracken, A.P.2
Pasini, D.3
Dietrich, N.4
Gehani, S.S.5
Monrad, A.6
Rappsilber, J.7
Lerdrup, M.8
Helin, K.9
-
51
-
-
70349952171
-
Role of the polycomb protein EED in the propagation of repressive histone marks
-
Margueron R., Justin N., Ohno K., Sharpe M. L., Son J., Drury W. J. III, Voigt P., Martin S. R., Taylor W. R., De Marco V., Pirrotta V., Reinberg D., Gamblin S. J., Role of the polycomb protein EED in the propagation of repressive histone marks Nature 2009 461 7265 762 767
-
(2009)
Nature
, vol.461
, Issue.7265
, pp. 762-767
-
-
Margueron, R.1
Justin, N.2
Ohno, K.3
Sharpe, M.L.4
Son, J.5
Drury III, W.J.6
Voigt, P.7
Martin, S.R.8
Taylor, W.R.9
De Marco, V.10
Pirrotta, V.11
Reinberg, D.12
Gamblin, S.J.13
-
52
-
-
78149285100
-
Cyclin-dependent kinases regulate epigenetic gene silencing through phosphorylation of EZH2
-
Chen S., Bohrer L. R., Rai A. N., Pan Y., Gan L., Zhou X., Bagchi A., Simon J. A., Huang H., Cyclin-dependent kinases regulate epigenetic gene silencing through phosphorylation of EZH2 Nature Cell Biology 2010 12 11 1108 1114
-
(2010)
Nature Cell Biology
, vol.12
, Issue.11
, pp. 1108-1114
-
-
Chen, S.1
Bohrer, L.R.2
Rai, A.N.3
Pan, Y.4
Gan, L.5
Zhou, X.6
Bagchi, A.7
Simon, J.A.8
Huang, H.9
-
53
-
-
78649807567
-
Phosphorylation of the PRC2 component Ezh2 is cell cycle-regulated and up-regulates its binding to ncRNA
-
Kaneko S., Li G., Son J., Xu C. F., Margueron R., Neubert T. A., Reinberg D., Phosphorylation of the PRC2 component Ezh2 is cell cycle-regulated and up-regulates its binding to ncRNA Genes and Development 2010 24 23 2615 2620
-
(2010)
Genes and Development
, vol.24
, Issue.23
, pp. 2615-2620
-
-
Kaneko, S.1
Li, G.2
Son, J.3
Xu, C.F.4
Margueron, R.5
Neubert, T.A.6
Reinberg, D.7
-
54
-
-
81755177803
-
PcG complexes set the stage for epigenetic inheritance of gene silencing in early S phase before replication
-
article e1002370
-
Lanzuolo C., Lo Sardo F., Diamantini A., Orlando V., PcG complexes set the stage for epigenetic inheritance of gene silencing in early S phase before replication PLoS Genetics 2011 7, article e1002370
-
(2011)
PLoS Genetics
, vol.7
-
-
Lanzuolo, C.1
Lo Sardo, F.2
Diamantini, A.3
Orlando, V.4
-
55
-
-
84860328967
-
Concerted epigenetic signatures inheritance at PcG targets through replication
-
Lanzuolo C., Lo Sardo F., Orlando V., Concerted epigenetic signatures inheritance at PcG targets through replication Cell Cycle 2012 11 7 1296 1300
-
(2012)
Cell Cycle
, vol.11
, Issue.7
, pp. 1296-1300
-
-
Lanzuolo, C.1
Lo Sardo, F.2
Orlando, V.3
-
56
-
-
80755176263
-
Chromosome silencing mechanisms in X-chromosome inactivation: Unknown unknowns
-
Brockdorff N., Chromosome silencing mechanisms in X-chromosome inactivation: unknown unknowns Development 2011 138 5057 5065
-
(2011)
Development
, vol.138
, pp. 5057-5065
-
-
Brockdorff, N.1
-
57
-
-
79959843359
-
Polycomb proteins in mammalian cell differentiation and plasticity
-
Prezioso C., Orlando V., Polycomb proteins in mammalian cell differentiation and plasticity FEBS Letters 2011 585 13 2067 2077
-
(2011)
FEBS Letters
, vol.585
, Issue.13
, pp. 2067-2077
-
-
Prezioso, C.1
Orlando, V.2
-
58
-
-
79953163994
-
Chromatin states in pluripotent, differentiated, and reprogrammed cells
-
Fisher C. L., Fisher A. G., Chromatin states in pluripotent, differentiated, and reprogrammed cells Current Opinion in Genetics and Development 2011 21 2 140 146
-
(2011)
Current Opinion in Genetics and Development
, vol.21
, Issue.2
, pp. 140-146
-
-
Fisher, C.L.1
Fisher, A.G.2
-
59
-
-
78751662908
-
The Polycomb complex PRC2 and its mark in life
-
Margueron R., Reinberg D., The Polycomb complex PRC2 and its mark in life Nature 2011 469 7330 343 349
-
(2011)
Nature
, vol.469
, Issue.7330
, pp. 343-349
-
-
Margueron, R.1
Reinberg, D.2
-
60
-
-
79955011376
-
Complexity of polycomb group function: Diverse mechanisms of target specificity
-
Trask M. C., Mager J., Complexity of polycomb group function: diverse mechanisms of target specificity Journal of Cellular Physiology 2011 226 7 1719 1721
-
(2011)
Journal of Cellular Physiology
, vol.226
, Issue.7
, pp. 1719-1721
-
-
Trask, M.C.1
Mager, J.2
-
61
-
-
79956302047
-
TET1 and hydroxymethylcytosine in transcription and DNA methylation fidelity
-
Williams K., Christensen J., Pedersen M. T., Johansen J. V., Cloos P. A. C., Rappsilber J., Helin K., TET1 and hydroxymethylcytosine in transcription and DNA methylation fidelity Nature 2011 473 7347 343 349
-
(2011)
Nature
, vol.473
, Issue.7347
, pp. 343-349
-
-
Williams, K.1
Christensen, J.2
Pedersen, M.T.3
Johansen, J.V.4
Cloos, P.A.C.5
Rappsilber, J.6
Helin, K.7
-
62
-
-
79956292024
-
Dual functions of Tet1 in transcriptional regulation in mouse embryonic stem cells
-
Wu H., D'Alessio A. C., Ito S., Xia K., Wang Z., Cui K., Zhao K., Eve Sun Y., Zhang Y., Dual functions of Tet1 in transcriptional regulation in mouse embryonic stem cells Nature 2011 473 7347 389 394
-
(2011)
Nature
, vol.473
, Issue.7347
, pp. 389-394
-
-
Wu, H.1
D'Alessio, A.C.2
Ito, S.3
Xia, K.4
Wang, Z.5
Cui, K.6
Zhao, K.7
Eve Sun, Y.8
Zhang, Y.9
-
63
-
-
79954457998
-
Genome-wide analysis of 5-hydroxymethylcytosine distribution reveals its dual function in transcriptional regulation in mouse embryonic stem cells
-
Wu H., D'Alessio A. C., Ito S., Wang Z., Cui K., Zhao K., Sun Y. E., Zhang Y., Genome-wide analysis of 5-hydroxymethylcytosine distribution reveals its dual function in transcriptional regulation in mouse embryonic stem cells Genes and Development 2011 25 7 679 684
-
(2011)
Genes and Development
, vol.25
, Issue.7
, pp. 679-684
-
-
Wu, H.1
D'Alessio, A.C.2
Ito, S.3
Wang, Z.4
Cui, K.5
Zhao, K.6
Sun, Y.E.7
Zhang, Y.8
-
64
-
-
33749015734
-
Molecular mechanisms of muscular dystrophies: Old and new players
-
DOI 10.1038/nrm2024, PII NRM2024
-
Davies K. E., Nowak K. J., Molecular mechanisms of muscular dystrophies: old and new players Nature Reviews Molecular Cell Biology 2006 7 10 762 773 (Pubitemid 44450460)
-
(2006)
Nature Reviews Molecular Cell Biology
, vol.7
, Issue.10
, pp. 762-773
-
-
Davies, K.E.1
Nowak, K.J.2
-
65
-
-
0028205618
-
Expression of dystrophin-associated proteins in dystrophin-positive muscle fibers (revertants) in Duchenne muscular dystrophy
-
DOI 10.1016/0960-8966(94)90002-7
-
Matsumura K., Tome F. M. S., Collin H., Leturcq F., Jeanpierre M., Kaplan J. C., Fardeau M., Campbell K. P., Expression of dystrophin-associated proteins in dystrophin-positive muscle fibers (revertants) in Duchenne muscular dystrophy Neuromuscular Disorders 1994 4 2 115 120 (Pubitemid 24124592)
-
(1994)
Neuromuscular Disorders
, vol.4
, Issue.2
, pp. 115-120
-
-
Matsumura, K.1
Tome, F.M.S.2
Collin, H.3
Leturcq, F.4
Jeanpierre, M.5
Kaplan, J.-C.6
Fardeau, M.7
Campbell, K.P.8
-
66
-
-
38949130017
-
Biology of the Striated Muscle Dystrophin-Glycoprotein Complex
-
DOI 10.1016/S0074-7696(07)65005-0, PII S0074769607650050, A Survey of Cell Biology
-
Ervasti J. M., Sonnemann K. J., Biology of the Striated Muscle Dystrophin-Glycoprotein Complex International Review of Cytology 2008 265 191 225 (Pubitemid 351215989)
-
(2008)
International Review of Cytology
, vol.265
, pp. 191-225
-
-
Ervasti, J.M.1
Sonnemann, K.J.2
-
67
-
-
58049221125
-
HDAC2 blockade by nitric oxide and histone deacetylase inhibitors reveals a common target in Duchenne muscular dystrophy treatment
-
Colussi C., Mozzetta C., Gurtner A., Illi B., Rosati J., Straino S., Ragone G., Pescatori M., Zaccagnini G., Antonini A., Minetti G., Martelli F., Piaggio G., Gallinari P., Steinkulher C., Clementi E., Dell'Aversana C., Altucci L., Mai A., Capogrossi M. C., Puri P. L., Gaetano C., HDAC2 blockade by nitric oxide and histone deacetylase inhibitors reveals a common target in Duchenne muscular dystrophy treatment Proceedings of the National Academy of Sciences of the United States of America 2008 105 49 19183 19187
-
(2008)
Proceedings of the National Academy of Sciences of the United States of America
, vol.105
, Issue.49
, pp. 19183-19187
-
-
Colussi, C.1
Mozzetta, C.2
Gurtner, A.3
Illi, B.4
Rosati, J.5
Straino, S.6
Ragone, G.7
Pescatori, M.8
Zaccagnini, G.9
Antonini, A.10
Minetti, G.11
Martelli, F.12
Piaggio, G.13
Gallinari, P.14
Steinkulher, C.15
Clementi, E.16
Dell'Aversana, C.17
Altucci, L.18
Mai, A.19
Capogrossi, M.C.20
Puri, P.L.21
Gaetano, C.22
more..
-
68
-
-
77957685944
-
MicroRNAs involved in molecular circuitries relevant for the duchenne muscular dystrophy pathogenesis are controlled by the dystrophin/nNOS pathway
-
Cacchiarelli D., Martone J., Girardi E., Cesana M., Incitti T., Morlando M., Nicoletti C., Santini T., Sthandier O., Barberi L., Auricchio A., Musar A., Bozzoni I., MicroRNAs involved in molecular circuitries relevant for the duchenne muscular dystrophy pathogenesis are controlled by the dystrophin/nNOS pathway Cell Metabolism 2010 12 4 341 351
-
(2010)
Cell Metabolism
, vol.12
, Issue.4
, pp. 341-351
-
-
Cacchiarelli, D.1
Martone, J.2
Girardi, E.3
Cesana, M.4
Incitti, T.5
Morlando, M.6
Nicoletti, C.7
Santini, T.8
Sthandier, O.9
Barberi, L.10
Auricchio, A.11
Musar, A.12
Bozzoni, I.13
-
69
-
-
79551594779
-
MiR-31 modulates dystrophin expression: New implications for Duchenne muscular dystrophy therapy
-
Cacchiarelli D., Incitti T., Martone J., Cesana M., Cazzella V., Santini T., Sthandier O., Bozzoni I., MiR-31 modulates dystrophin expression: new implications for Duchenne muscular dystrophy therapy EMBO Reports 2011 12 2 136 141
-
(2011)
EMBO Reports
, vol.12
, Issue.2
, pp. 136-141
-
-
Cacchiarelli, D.1
Incitti, T.2
Martone, J.3
Cesana, M.4
Cazzella, V.5
Santini, T.6
Sthandier, O.7
Bozzoni, I.8
-
70
-
-
33749507982
-
Functional and morphological recovery of dystrophic muscles in mice treated with deacetylase inhibitors
-
DOI 10.1038/nm1479, PII NM1479
-
Minetti G. C., Colussi C., Adami R., Serra C., Mozzetta C., Parente V., Fortuni S., Straino S., Sampaolesi M., Di Padova M., Illi B., Gallinari P., Steinkhler C., Capogrossi M. C., Sartorelli V., Bottinelli R., Gaetano C., Puri P. L., Functional and morphological recovery of dystrophic muscles in mice treated with deacetylase inhibitors Nature Medicine 2006 12 10 1147 1150 (Pubitemid 44527349)
-
(2006)
Nature Medicine
, vol.12
, Issue.10
, pp. 1147-1150
-
-
Minetti, G.C.1
Colussi, C.2
Adami, R.3
Serra, C.4
Mozzetta, C.5
Parente, V.6
Fortuni, S.7
Straino, S.8
Sampaolesi, M.9
Di Padova, M.10
Illi, B.11
Gallinari, P.12
Steinkuhler, C.13
Capogrossi, M.C.14
Sartorelli, V.15
Bottinelli, R.16
Gaetano, C.17
Puri, P.L.18
-
71
-
-
79957948651
-
Histone deacetylase inhibitors in the treatment of muscular dystrophies: Epigenetic drugs for genetic diseases
-
Consalvi S., Saccone V., Giordani L., Minetti G., Mozzetta C., Puri P. L., Histone deacetylase inhibitors in the treatment of muscular dystrophies: epigenetic drugs for genetic diseases Molecular Medicine 2011 17 5-6 457 465
-
(2011)
Molecular Medicine
, vol.17
, Issue.56
, pp. 457-465
-
-
Consalvi, S.1
Saccone, V.2
Giordani, L.3
Minetti, G.4
Mozzetta, C.5
Puri, P.L.6
-
72
-
-
80052033608
-
Myotonic dystrophy mouse models: Towards rational therapy development
-
Gomes-Pereira M., Cooper T. A., Gourdon G., Myotonic dystrophy mouse models: towards rational therapy development Trends in Molecular Medicine 2011 17 9 506 517
-
(2011)
Trends in Molecular Medicine
, vol.17
, Issue.9
, pp. 506-517
-
-
Gomes-Pereira, M.1
Cooper, T.A.2
Gourdon, G.3
-
73
-
-
15044354661
-
RNA pathogenesis of the myotonic dystrophies
-
DOI 10.1016/j.nmd.2004.09.012
-
Day J. W., Ranum L. P. W., RNA pathogenesis of the myotonic dystrophies Neuromuscular Disorders 2005 15 1 5 16 (Pubitemid 41556627)
-
(2005)
Neuromuscular Disorders
, vol.15
, Issue.1
, pp. 5-16
-
-
Day, J.W.1
Ranum, L.P.W.2
-
74
-
-
33646882068
-
Polycomb complexes repress developmental regulators in murine embryonic stem cells
-
DOI 10.1038/nature04733, PII NATURE04733
-
Boyer L. A., Plath K., Zeitlinger J., Brambrink T., Medeiros L. A., Lee T. I., Levine S. S., Wernig M., Tajonar A., Ray M. K., Bell G. W., Otte A. P., Vidal M., Gifford D. K., Young R. A., Jaenisch R., Polycomb complexes repress developmental regulators in murine embryonic stem cells Nature 2006 441 7091 349 353 (Pubitemid 44050199)
-
(2006)
Nature
, vol.441
, Issue.7091
, pp. 349-353
-
-
Boyer, L.A.1
Plath, K.2
Zeitlinger, J.3
Brambrink, T.4
Medeiros, L.A.5
Lee, T.I.6
Levine, S.S.7
Wernig, M.8
Tajonar, A.9
Ray, M.K.10
Bell, G.W.11
Otte, A.P.12
Vidal, M.13
Gifford, D.K.14
Young, R.A.15
Jaenisch, R.16
-
75
-
-
33646870495
-
Genome-wide mapping of polycomb target genes unravels their roles in cell fate transitions
-
Bracken A. P., Dietrich N., Pasini D., Hansen K. H., Helin K., Genome-wide mapping of polycomb target genes unravels their roles in cell fate transitions Genes and Development 2006 20 9 1123 1136
-
(2006)
Genes and Development
, vol.20
, Issue.9
, pp. 1123-1136
-
-
Bracken, A.P.1
Dietrich, N.2
Pasini, D.3
Hansen, K.H.4
Helin, K.5
-
76
-
-
33646865180
-
Control of developmental regulators by polycomb in human embryonic stem cells
-
DOI 10.1016/j.cell.2006.02.043, PII S0092867406003849
-
Lee T. I., Jenner R. G., Boyer L. A., Guenther M. G., Levine S. S., Kumar R. M., Chevalier B., Johnstone S. E., Cole M. F., Isono K. I., Koseki H., Fuchikami T., Abe K., Murray H. L., Zucker J. P., Yuan B., Bell G. W., Herbolsheimer E., Hannett N. M., Sun K., Odom D. T., Otte A. P., Volkert T. L., Bartel D. P., Melton D. A., Gifford D. K., Jaenisch R., Young R. A., Control of developmental regulators by polycomb in human embryonic stem cells Cell 2006 125 2 301 313 (Pubitemid 44313811)
-
(2006)
Cell
, vol.125
, Issue.2
, pp. 301-313
-
-
Lee, T.I.1
Jenner, R.G.2
Boyer, L.A.3
Guenther, M.G.4
Levine, S.S.5
Kumar, R.M.6
Chevalier, B.7
Johnstone, S.E.8
Cole, M.F.9
Isono, K.-i.10
Koseki, H.11
Fuchikami, T.12
Abe, K.13
Murray, H.L.14
Zucker, J.P.15
Yuan, B.16
Bell, G.W.17
Herbolsheimer, E.18
Hannett, N.M.19
Sun, K.20
Odom, D.T.21
Otte, A.P.22
Volkert, T.L.23
Bartel, D.P.24
Melton, D.A.25
Gifford, D.K.26
Jaenisch, R.27
Young, R.A.28
more..
-
77
-
-
33646856965
-
Chromosomal distribution of PcG proteins during Drosophila development
-
ARTICLE E170
-
Ngre N., Hennetin J., Sun L. V., Lavrov S., Bellis M., White K. P., Cavalli G., Chromosomal distribution of PcG proteins during Drosophila development PLoS Biology 2006 4 6, article e170
-
(2006)
PLoS Biology
, vol.4
, Issue.6
-
-
Ngre, N.1
Hennetin, J.2
Sun, L.V.3
Lavrov, S.4
Bellis, M.5
White, K.P.6
Cavalli, G.7
-
78
-
-
33745225872
-
Genome-wide analysis of Polycomb targets in Drosophila melanogaster
-
DOI 10.1038/ng1817, PII N1817
-
Schwartz Y. B., Kahn T. G., Nix D. A., Li X. Y., Bourgon R., Biggin M., Pirrotta V., Genome-wide analysis of Polycomb targets in Drosophila melanogaster Nature Genetics 2006 38 6 700 705 (Pubitemid 43927314)
-
(2006)
Nature Genetics
, vol.38
, Issue.6
, pp. 700-705
-
-
Schwartz, Y.B.1
Kahn, T.G.2
Nix, D.A.3
Li, X.-Y.4
Bourgon, R.5
Biggin, M.6
Pirrotta, V.7
-
79
-
-
33745604636
-
Suz12 binds to silenced regions of the genome in a cell-type-specific manner
-
DOI 10.1101/gr.5306606
-
Squazzo S. L., O'Geen H., Komashko V. M., Krig S. R., Jin V. X., Jang S. W., Margueron R., Reinberg D., Green R., Farnham P. J., Suz12 binds to silenced regions of the genome in a cell-type-specific manner Genome Research 2006 16 7 890 900 (Pubitemid 43992913)
-
(2006)
Genome Research
, vol.16
, Issue.7
, pp. 890-900
-
-
Squazzo, S.L.1
O'Geen, H.2
Komashko, V.M.3
Krig, S.R.4
Jin, V.X.5
Jang, S.-W.6
Margueron, R.7
Reinberg, D.8
Green, R.9
Farnham, P.J.10
-
80
-
-
33745258986
-
Genome-wide profiling of PRC1 and PRC2 Polycomb chromatin binding in Drosophila melanogaster
-
DOI 10.1038/ng1792, PII N1792
-
Tolhuis B., Muijrers I., De Wit E., Teunissen H., Talhout W., Van Steensel B., Van Lohuizen M., Genome-wide profiling of PRC1 and PRC2 Polycomb chromatin binding in Drosophila melanogaster Nature Genetics 2006 38 6 694 699 (Pubitemid 43927313)
-
(2006)
Nature Genetics
, vol.38
, Issue.6
, pp. 694-699
-
-
Tolhuis, B.1
Muijrers, I.2
De Wit, E.3
Teunissen, H.4
Talhout, W.5
Van Steensel, B.6
Van Lohuizen, M.7
-
81
-
-
79959349283
-
Genome-wide remodeling of the epigenetic landscape during myogenic differentiation
-
Asp P., Blum R., Vethantham V., Parisi F., Micsinai M., Cheng J., Bowman C., Kluger Y., Dynlacht B. D., Genome-wide remodeling of the epigenetic landscape during myogenic differentiation Proceedings of the National Academy of Sciences of the United States of America 2011 108 22 E149 E158
-
(2011)
Proceedings of the National Academy of Sciences of the United States of America
, vol.108
, Issue.22
-
-
Asp, P.1
Blum, R.2
Vethantham, V.3
Parisi, F.4
Micsinai, M.5
Cheng, J.6
Bowman, C.7
Kluger, Y.8
Dynlacht, B.D.9
-
82
-
-
7544230144
-
The Polycomb Ezh2 methyltransferase regulates muscle gene expression and skeletal muscle differentiation
-
DOI 10.1101/gad.1241904
-
Caretti G., Di Padova M., Micales B., Lyons G. E., Sartorelli V., The Polycomb Ezh2 methyltransferase regulates muscle gene expression and skeletal muscle differentiation Genes and Development 2004 18 2627 2638 (Pubitemid 39453102)
-
(2004)
Genes and Development
, vol.18
, Issue.21
, pp. 2627-2638
-
-
Caretti, G.1
Di Padova, M.2
Micales, B.3
Lyons, G.E.4
Sartorelli, V.5
-
83
-
-
70349764482
-
Mir-214-dependent regulation of the polycomb protein Ezh2 in skeletal muscle and embryonic stem cells
-
Juan A. H., Kumar R. M., Marx J. G., Young R. A., Sartorelli V., Mir-214-dependent regulation of the polycomb protein Ezh2 in skeletal muscle and embryonic stem cells Molecular Cell 2009 36 1 61 74
-
(2009)
Molecular Cell
, vol.36
, Issue.1
, pp. 61-74
-
-
Juan, A.H.1
Kumar, R.M.2
Marx, J.G.3
Young, R.A.4
Sartorelli, V.5
-
84
-
-
80052571043
-
Chromatin regulated interchange between polycomb repressive complex 2 (PRC2)-Ezh2 and PRC2-Ezh1 complexes controls myogenin activation in skeletal muscle cells
-
Stojic L., Jasencakova Z., Prezioso C., Stutzer A., Bodega B., Chromatin regulated interchange between polycomb repressive complex 2 (PRC2)-Ezh2 and PRC2-Ezh1 complexes controls myogenin activation in skeletal muscle cells Epigenetics Chromatin 2011 4, article 16
-
(2011)
Epigenetics Chromatin
, vol.416
-
-
Stojic, L.1
Jasencakova, Z.2
Prezioso, C.3
Stutzer, A.4
Bodega, B.5
-
85
-
-
79955459714
-
Polycomb EZH2 controls self-renewal and safeguards the transcriptional identity of skeletal muscle stem cells
-
Juan A. H., Derfoul A., Feng X., Ryall J. G., Dell'Orso S., Pasut A., Zare H., Simone J. M., Rudnicki M. A., Sartorelli V., Polycomb EZH2 controls self-renewal and safeguards the transcriptional identity of skeletal muscle stem cells Genes and Development 2011 25 8 789 794
-
(2011)
Genes and Development
, vol.25
, Issue.8
, pp. 789-794
-
-
Juan, A.H.1
Derfoul, A.2
Feng, X.3
Ryall, J.G.4
Dell'Orso, S.5
Pasut, A.6
Zare, H.7
Simone, J.M.8
Rudnicki, M.A.9
Sartorelli, V.10
-
86
-
-
80054715378
-
A long noncoding RNA controls muscle differentiation by functioning as a competing endogenous RNA
-
Cesana M., Cacchiarelli D., Legnini I., Santini T., Sthandier O., A long noncoding RNA controls muscle differentiation by functioning as a competing endogenous RNA Cell 2011 147 358 369
-
(2011)
Cell
, vol.147
, pp. 358-369
-
-
Cesana, M.1
Cacchiarelli, D.2
Legnini, I.3
Santini, T.4
Sthandier, O.5
-
87
-
-
77954122499
-
In junk we trust: Repetitive DNA, epigenetics and facioscapulohumeral muscular dystrophy
-
Neguembor M. V., Gabellini D., In junk we trust: repetitive DNA, epigenetics and facioscapulohumeral muscular dystrophy Epigenomics 2010 2 2 271 287
-
(2010)
Epigenomics
, vol.2
, Issue.2
, pp. 271-287
-
-
Neguembor, M.V.1
Gabellini, D.2
-
88
-
-
77957357566
-
TNF/p38 /polycomb signaling to Pax7 locus in satellite cells links inflammation to the epigenetic control of muscle regeneration
-
Palacios D., Mozzetta C., Consalvi S., Caretti G., Saccone V., Proserpio V., Marquez V. E., Valente S., Mai A., Forcales S. V., Sartorelli V., Puri P. L., TNF/p38 /polycomb signaling to Pax7 locus in satellite cells links inflammation to the epigenetic control of muscle regeneration Cell Stem Cell 2010 7 4 455 469
-
(2010)
Cell Stem Cell
, vol.7
, Issue.4
, pp. 455-469
-
-
Palacios, D.1
Mozzetta, C.2
Consalvi, S.3
Caretti, G.4
Saccone, V.5
Proserpio, V.6
Marquez, V.E.7
Valente, S.8
Mai, A.9
Forcales, S.V.10
Sartorelli, V.11
Puri, P.L.12
-
89
-
-
80054000315
-
An EDMD mutation in C. elegans lamin blocks muscle-specific gene relocation and compromises muscle integrity
-
Mattout A., Pike B. L., Towbin B. D., Bank E. M., Gonzalez-Sandoval A., et al., An EDMD mutation in C. elegans lamin blocks muscle-specific gene relocation and compromises muscle integrity Current Biology 2011 21 1603 1614
-
(2011)
Current Biology
, vol.21
, pp. 1603-1614
-
-
Mattout, A.1
Pike, B.L.2
Towbin, B.D.3
Bank, E.M.4
Gonzalez-Sandoval, A.5
Et Al.6
-
90
-
-
33745715007
-
Facioscapulohumeral muscular dystrophy
-
Tawil R., Van Der Maarel S. M., Facioscapulohumeral muscular dystrophy Muscle and Nerve 2006 34 1 1 15
-
(2006)
Muscle and Nerve
, vol.34
, Issue.1
, pp. 1-15
-
-
Tawil, R.1
Van Der Maarel, S.M.2
-
91
-
-
0027528536
-
Extreme variability of expression in monozygotic twins with FSH muscular dystrophy
-
Tawil R., Storvick D., Feasby T. E., Weiffenbach B., Griggs R. C., Extreme variability of expression in monozygotic twins with FSH muscular dystrophy Neurology 1993 43 2 345 348 (Pubitemid 23060267)
-
(1993)
Neurology
, vol.43
, Issue.2
, pp. 345-348
-
-
Tawil, R.1
Storvick, D.2
Feasby, T.E.3
Weiffenbach, B.4
Griggs, R.C.5
-
92
-
-
0028952903
-
Monozygotic twins with facioscapulohumeral dystrophy (FSHD): Implications for genotype/phenotype correlation
-
Griggs R. C., Tawil R., McDermott M., Forrester J., Figlewicz D., Weiffenbach B., Monozygotic twins with facioscapulohumeral dystrophy (FSHD): implications for genotype/phenotype correlation Muscle and Nerve 1995 18 2 S50 S55
-
(1995)
Muscle and Nerve
, vol.18
, Issue.2
-
-
Griggs, R.C.1
Tawil, R.2
McDermott, M.3
Forrester, J.4
Figlewicz, D.5
Weiffenbach, B.6
-
93
-
-
0027744223
-
FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit
-
Van Deutekom J. C. T., Wijmenga C., Van Tienhoven E. A. E., Gruter A. M., Hewitt J. E., Padberg G. W., Van Ommen G. J. B., Hofker M. H., Frants R. R., FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit Human Molecular Genetics 1993 2 12 2037 2042 (Pubitemid 24003395)
-
(1993)
Human Molecular Genetics
, vol.2
, Issue.12
, pp. 2037-2042
-
-
Van Deutekom, J.C.T.1
Wijmenga, C.2
Van Tienhoven, E.A.E.3
Gruter, A.-M.4
Hewitt, J.E.5
Padberg, G.W.6
Van Ommen, G.-J.B.7
Hofker, M.H.8
Frants, R.R.9
-
94
-
-
0029827344
-
Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: Implications for genetic counselling and etiology of FSHD1
-
van Deutekom J. C. T., Bakker E., Lemmers R. J. L. F., Van Der Wielen M. J. R., Bik E., Hofker M. H., Padberg G. W., Frants R. R., Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: implications for genetic counselling and etiology of FSHD1 Human Molecular Genetics 1996 5 12 1997 2003 (Pubitemid 26413645)
-
(1996)
Human Molecular Genetics
, vol.5
, Issue.12
, pp. 1997-2003
-
-
Van Deutekom, J.C.T.1
Bakker, E.2
Lemmers, R.J.L.F.3
Van Der Wielen, M.J.R.4
Bik, E.5
Hofker, M.H.6
Padberg, G.W.7
Frants, R.R.8
-
95
-
-
0029038951
-
Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD)
-
Lunt P. W., Jardine P. E., Koch M. C., Maynard J., Osborn M., Williams M., Harper P. S., Upadhyaya M., Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD) Human Molecular Genetics 1995 4 5 951 958
-
(1995)
Human Molecular Genetics
, vol.4
, Issue.5
, pp. 951-958
-
-
Lunt, P.W.1
Jardine, P.E.2
Koch, M.C.3
Maynard, J.4
Osborn, M.5
Williams, M.6
Harper, P.S.7
Upadhyaya, M.8
-
96
-
-
0032978703
-
Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype
-
DOI 10.1002/1531-8249(199906)45:6 <751::AID-ANA9> 3.0.CO;2-M
-
Ricci E., Galluzzi G., Deidda G., Cacurri S., Colantoni L., Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype Annals of Neurology 1999 45 751 757 (Pubitemid 29260752)
-
(1999)
Annals of Neurology
, vol.45
, Issue.6
, pp. 751-757
-
-
Ricci, E.1
Galluzzi, G.2
Deidda, G.3
Cacurri, S.4
Colantoni, L.5
Merico, B.6
Piazzo, N.7
Servidei, S.8
Vigneti, E.9
Pasceri, V.10
Silvestri, G.11
Mirabella, M.12
Mangiola, F.13
Tonali, P.14
Felicetti, L.15
-
97
-
-
0029984970
-
Evidence for anticipation and association of deletion size with severity in facioscapulohumeral muscular systrophy
-
Tawil R., Forrester J., Griggs R. C., Mendell J., Kissel J., McDermott M., King W., Weiffenbach B., Figlewicz D., Cos L., Langsam A., Pandya S., Martens B., Brower C., Herr B., Downing K., Evidence for anticipation and association of deletion size with severity in facioscapulohumeral muscular systrophy Annals of Neurology 1996 39 6 744 748
-
(1996)
Annals of Neurology
, vol.39
, Issue.6
, pp. 744-748
-
-
Tawil, R.1
Forrester, J.2
Griggs, R.C.3
Mendell, J.4
Kissel, J.5
McDermott, M.6
King, W.7
Weiffenbach, B.8
Figlewicz, D.9
Cos, L.10
Langsam, A.11
Pandya, S.12
Martens, B.13
Brower, C.14
Herr, B.15
Downing, K.16
-
98
-
-
0030009384
-
Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy
-
Tupler R., Berardinelli A., Barbierato L., Frants R., Hewitt J. E., Lanzi G., Maraschio P., Tiepolo L., Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy Journal of Medical Genetics 1996 33 5 366 370 (Pubitemid 26147866)
-
(1996)
Journal of Medical Genetics
, vol.33
, Issue.5
, pp. 366-370
-
-
Tupler, R.1
Berardinelli, A.2
Barbierato, L.3
Frants, R.4
Hewitt, J.E.5
Lanzi, G.6
Maraschio, P.7
Tiepolo, L.8
-
99
-
-
0036788610
-
Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere
-
Lemmers R. J. L. F., De Kievit P., Sandkuijl L., Padberg G. W., Van Ommen G. J. B., Frants R. R., Van der Maarel S. M., Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere Nature Genetics 2002 32 2 235 236
-
(2002)
Nature Genetics
, vol.32
, Issue.2
, pp. 235-236
-
-
Lemmers, R.J.L.F.1
De Kievit, P.2
Sandkuijl, L.3
Padberg, G.W.4
Van Ommen, G.J.B.5
Frants, R.R.6
Van Der Maarel, S.M.7
-
100
-
-
77957327192
-
A unifying genetic model for facioscapulohumeral muscular dystrophy
-
Lemmers R. J. L. F., Van Der Vliet P. J., Klooster R., Sacconi S., Camao P., Dauwerse J. G., Snider L., Straasheijm K. R., Van Ommen G. J., Padberg G. W., Miller D. G., Tapscott S. J., Tawil R., Frants R. R., Van Der Maarel S. M., A unifying genetic model for facioscapulohumeral muscular dystrophy Science 2010 329 5999 1650 1653
-
(2010)
Science
, vol.329
, Issue.5999
, pp. 1650-1653
-
-
Lemmers, R.J.L.F.1
Van Der Vliet, P.J.2
Klooster, R.3
Sacconi, S.4
Camao, P.5
Dauwerse, J.G.6
Snider, L.7
Straasheijm, K.R.8
Van Ommen, G.J.9
Padberg, G.W.10
Miller, D.G.11
Tapscott, S.J.12
Tawil, R.13
Frants, R.R.14
Van Der Maarel, S.M.15
-
101
-
-
8844227430
-
Contractions of D4Z4 on 4qB subtelomeres do not cause facioscapulohumeral muscular dystrophy
-
DOI 10.1086/426035
-
Lemmers R. J. F. L., Wohlgemuth M., Frants R. R., Padberg G. W., Morava E., Van Der Maarel S. M., Contractions of D4Z4 on 4qB subtelomeres do not cause facioscapulohumeral muscular dystrophy American Journal of Human Genetics 2004 75 6 1124 1130 (Pubitemid 39532080)
-
(2004)
American Journal of Human Genetics
, vol.75
, Issue.6
, pp. 1124-1130
-
-
Lemmers, R.J.F.L.1
Wohlgemuth, M.2
Frants, R.R.3
Padberg, G.W.4
Morava, E.5
Van Der Maarel, S.M.6
-
102
-
-
34147177128
-
A large patient study confirming that facioscapulohumeral muscular dystrophy (FSHD) disease expression is almost exclusively associated with an FSHD locus located on a 4qA-defined 4qter subtelomere
-
DOI 10.1136/jmg.2006.042804
-
Thomas N. S. T., Wiseman K., Spurlock G., MacDonald M., stek D., Upadhyaya M., A large patient study confirming that facioscapulohumeral muscular dystrophy (FSHD) disease expression is almost exclusively associated with an FSHD locus located on a 4qA-defined 4qter subtelomere Journal of Medical Genetics 2007 44 3 215 218 (Pubitemid 46580532)
-
(2007)
Journal of Medical Genetics
, vol.44
, Issue.3
, pp. 215-218
-
-
Thomas, N.S.T.1
Wiseman, K.2
Spurlock, G.3
MacDonald, M.4
Ustek, D.5
Upadhyaya, M.6
-
103
-
-
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 arms of the acrocentric chromosomes
-
Lyle R., Wright T. J., Clark L. N., Hewitt J. E., The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes Genomics 1995 28 3 389 397
-
(1995)
Genomics
, vol.28
, Issue.3
, pp. 389-397
-
-
Lyle, R.1
Wright, T.J.2
Clark, L.N.3
Hewitt, J.E.4
-
104
-
-
0028911841
-
The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qter
-
Bakker E., Wijmenga C., Vossen R. H. A. M., Padberg G. W., Hewitt J., Van der Wielen M., Rasmussen K., Frants R. R., The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qter Muscle and Nerve 1995 18 2 S39 S44
-
(1995)
Muscle and Nerve
, vol.18
, Issue.2
-
-
Bakker, E.1
Wijmenga, C.2
Vossen, R.H.A.M.3
Padberg, G.W.4
Hewitt, J.5
Van Der Wielen, M.6
Rasmussen, K.7
Frants, R.R.8
-
105
-
-
0029041708
-
Physical mapping evidence for a duplicated region on chromosome 10qter showing high homology with the facioscapulohumeral muscular dystrophy locus on chromosome 4qter
-
Deidda G., Cacurri S., Grisanti P., Vigneti E., Piazzo N., Felicetti L., Physical mapping evidence for a duplicated region on chromosome 10qter showing high homology with the facioscapulohumeral muscular dystrophy locus on chromosome 4qter European Journal of Human Genetics 1995 3 3 155 167
-
(1995)
European Journal of Human Genetics
, vol.3
, Issue.3
, pp. 155-167
-
-
Deidda, G.1
Cacurri, S.2
Grisanti, P.3
Vigneti, E.4
Piazzo, N.5
Felicetti, L.6
-
106
-
-
0035194812
-
Complete allele information in the diagnosis of facioscapulohumeral muscular dystrophy by triple DNA analysis
-
DOI 10.1002/ana.10057
-
Lemmers R. J. L. F., de Kievit P., van Geel M., Van Der Wielen M. J. R., Bakker E., Padberg G. W., Frants R. R., Van Der Maarel S. M., Complete allele information in the diagnosis of facioscapulohumeral muscular dystrophy by triple DNA analysis Annals of Neurology 2001 50 6 816 819 (Pubitemid 33116145)
-
(2001)
Annals of Neurology
, vol.50
, Issue.6
, pp. 816-819
-
-
Lemmers, R.J.L.F.1
De Kievit, P.2
Van Geel, M.3
Van Der Wielen, M.J.R.4
Bakker, E.5
Padberg, G.W.6
Frants, R.R.7
Van Der Maarel, S.M.8
-
107
-
-
0037047439
-
Inappropriate gene activation in FSHD: A repressor complex binds a chromosomal repeat deleted in dystrophic muscle
-
Gabellini D., Green M. R., Tupler R., Inappropriate gene activation in FSHD: a repressor complex binds a chromosomal repeat deleted in dystrophic muscle Cell 2002 110 3 339 348
-
(2002)
Cell
, vol.110
, Issue.3
, pp. 339-348
-
-
Gabellini, D.1
Green, M.R.2
Tupler, R.3
-
108
-
-
69149087644
-
Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiation
-
Bodega B., Ramirez G. D., Grasser F., Cheli S., Brunelli S., Mora M., Meneveri R., Marozzi A., Mueller S., Battaglioli E., Ginelli E., Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiation BMC Biology 2009 7, article 41
-
(2009)
BMC Biology
, vol.741
-
-
Bodega, B.1
Ramirez, G.D.2
Grasser, F.3
Cheli, S.4
Brunelli, S.5
Mora, M.6
Meneveri, R.7
Marozzi, A.8
Mueller, S.9
Battaglioli, E.10
Ginelli, E.11
-
109
-
-
33644522383
-
Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1
-
DOI 10.1038/nature04422, PII N04422
-
Gabellini D., D'Antona G., Moggio M., Prelle A., Zecca C., Adami R., Angeletti B., Ciscato P., Pellegrino M. A., Bottinelli R., Green M. R., Tupler R., Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1 Nature 2006 439 7079 973 977 (Pubitemid 43292415)
-
(2006)
Nature
, vol.439
, Issue.7079
, pp. 973-977
-
-
Gabellini, D.1
D'Antona, G.2
Moggio, M.3
Prelle, A.4
Zecca, C.5
Adami, R.6
Angeletti, B.7
Ciscato, P.8
Pellegrino, M.A.9
Bottinelli, R.10
Green, M.R.11
Tupler, R.12
-
110
-
-
0345227304
-
Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q
-
DOI 10.1093/hmg/ddg323
-
Jiang G., Yang F., van Overveld P. G. M., Vedanarayanan V., van der Maarel S., Ehrlich M., Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q Human Molecular Genetics 2003 12 22 2909 2921 (Pubitemid 37442019)
-
(2003)
Human Molecular Genetics
, vol.12
, Issue.22
, pp. 2909-2921
-
-
Jiang, G.1
Yang, F.2
Van Overveld, P.G.M.3
Vedanarayanan, V.4
Van Der Maarel, S.5
Ehrlich, M.6
-
111
-
-
33847234593
-
Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy
-
Osborne R. J., Welle S., Venance S. L., Thornton C. A., Tawil R., Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy Neurology 2007 68 8 569 577
-
(2007)
Neurology
, vol.68
, Issue.8
, pp. 569-577
-
-
Osborne, R.J.1
Welle, S.2
Venance, S.L.3
Thornton, C.A.4
Tawil, R.5
-
112
-
-
2342572330
-
FRG1P is localised in the nucleolus, Cajal bodies, and speckles
-
ARTICLE E46
-
Van Koningsbruggen S., Dirks R. W., Mommaas A. M., Onderwater J. J., Deidda G., Padberg G. W., Frants R. R., Van Der Maarel S. M., FRG1P is localised in the nucleolus, Cajal bodies, and speckles Journal of Medical Genetics 2004 41 4, article e46
-
(2004)
Journal of Medical Genetics
, vol.41
, Issue.4
-
-
Van Koningsbruggen, S.1
Dirks, R.W.2
Mommaas, A.M.3
Onderwater, J.J.4
Deidda, G.5
Padberg, G.W.6
Frants, R.R.7
Van Der Maarel, S.M.8
-
113
-
-
33846589302
-
FRG1P-mediated aggregation of proteins involved in pre-mRNA processing
-
DOI 10.1007/s00412-006-0083-3
-
van Koningsbruggen S., Straasheijm K. R., Sterrenburg E., de Graaf N., Dauwerse H. G., Frants R. R., van der Maarel S. M., FRG1P-mediated aggregation of proteins involved in pre-mRNA processing Chromosoma 2007 116 1 53 64 (Pubitemid 46179022)
-
(2007)
Chromosoma
, vol.116
, Issue.1
, pp. 53-64
-
-
Van Koningsbruggen, S.1
Straasheijm, K.R.2
Sterrenburg, E.3
De Graaf, N.4
Dauwerse, H.G.5
Frants, R.R.6
Van Der Maarel, S.M.7
-
114
-
-
78449250235
-
Facioscapulohumeral dystrophy: Incomplete suppression of a retrotransposed gene
-
ARTICLE E1001181
-
Snider L., Geng L. N., Lemmers R. J., Kyba M., Ware C. B., Nelson A. M., Tawil R., Filippova G. N., van der Maarel S. M., Tapscott S. J., Miller D. G., Facioscapulohumeral dystrophy: incomplete suppression of a retrotransposed gene PLoS Genetics 2010 6 10, article e1001181
-
(2010)
PLoS Genetics
, vol.6
, Issue.10
-
-
Snider, L.1
Geng, L.N.2
Lemmers, R.J.3
Kyba, M.4
Ware, C.B.5
Nelson, A.M.6
Tawil, R.7
Filippova, G.N.8
Van Der Maarel, S.M.9
Tapscott, S.J.10
Miller, D.G.11
-
115
-
-
36749026295
-
DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1
-
DOI 10.1073/pnas.0708659104
-
Dixit M., Ansseau E., Tassin A., Winokur S., Shi R., Qian H., Sauvage S., Mattéotti C., Van Acker A. M., Leo O., Figlewicz D., Barro M., Laoudj-Chenivesse D., Belayew A., Coppée F., Chen Y. W., DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1 Proceedings of the National Academy of Sciences of the United States of America 2007 104 46 18157 18162 (Pubitemid 350210837)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.46
, pp. 18157-18162
-
-
Dixit, M.1
Ansseau, E.2
Tassin, A.3
Winokur, S.4
Shi, R.5
Qian, H.6
Sauvage, S.7
Matteotti, C.8
Van Acker, A.M.9
Leo, O.10
Figlewicz, D.11
Barro, M.12
Laoudj-Chenivesse, D.13
Belayew, A.14
Coppee, F.15
Chen, Y.-W.16
-
116
-
-
67249104052
-
RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: New candidates for the pathophysiology of facioscapulohumeral dystrophy
-
Snider L., Asawachaicharn A., Tyler A. E., Geng L. N., Petek L. M., Maves L., Miller D. G., Lemmers R. J. L. F., Winokur S. T., Tawil R., van der Maarel S. M., Filippova G. N., Tapscott S. J., RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: new candidates for the pathophysiology of facioscapulohumeral dystrophy Human Molecular Genetics 2009 18 13 2414 2430
-
(2009)
Human Molecular Genetics
, vol.18
, Issue.13
, pp. 2414-2430
-
-
Snider, L.1
Asawachaicharn, A.2
Tyler, A.E.3
Geng, L.N.4
Petek, L.M.5
Maves, L.6
Miller, D.G.7
Lemmers, R.J.L.F.8
Winokur, S.T.9
Tawil, R.10
Van Der Maarel, S.M.11
Filippova, G.N.12
Tapscott, S.J.13
-
117
-
-
34447104322
-
The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein
-
DOI 10.1016/j.nmd.2007.04.002, PII S0960896607001216
-
Kowaljow V., Marcowycz A., Ansseau E., Conde C. B., Sauvage S., Mattéotti C., Arias C., Corona E. D., Nuez N. G., Leo O., Wattiez R., Figlewicz D., Laoudj-Chenivesse D., Belayew A., Coppée F., Rosa A. L., The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein Neuromuscular Disorders 2007 17 8 611 623 (Pubitemid 47030917)
-
(2007)
Neuromuscular Disorders
, vol.17
, Issue.8
, pp. 611-623
-
-
Kowaljow, V.1
Marcowycz, A.2
Ansseau, E.3
Conde, C.B.4
Sauvage, S.5
Matteotti, C.6
Arias, C.7
Corona, E.D.8
Nunez, N.G.9
Leo, O.10
Wattiez, R.11
Figlewicz, D.12
Laoudj-Chenivesse, D.13
Belayew, A.14
Coppee, F.15
Rosa, A.L.16
-
118
-
-
53949112045
-
DUX4c, an FSHD candidate gene, interferes with myogenic regulators and abolishes myoblast differentiation
-
Bosnakovski D., Lamb S., Simsek T., Xu Z., Belayew A., Perlingeiro R., Kyba M., DUX4c, an FSHD candidate gene, interferes with myogenic regulators and abolishes myoblast differentiation Experimental Neurology 2008 214 1 87 96
-
(2008)
Experimental Neurology
, vol.214
, Issue.1
, pp. 87-96
-
-
Bosnakovski, D.1
Lamb, S.2
Simsek, T.3
Xu, Z.4
Belayew, A.5
Perlingeiro, R.6
Kyba, M.7
-
119
-
-
84855956147
-
DUX4 activates germline genes, retroelements, and immune mediators: Implications for facioscapulohumeral dystrophy
-
Geng L. N., Yao Z., Snider L., Fong A. P., Cech J. N., DUX4 activates germline genes, retroelements, and immune mediators: implications for facioscapulohumeral dystrophy Developmental Cell 2012 22 38 51
-
(2012)
Developmental Cell
, vol.22
, pp. 38-51
-
-
Geng, L.N.1
Yao, Z.2
Snider, L.3
Fong, A.P.4
Cech, J.N.5
-
120
-
-
78650148935
-
FSHD: Copy number variations on the theme of muscular dystrophy
-
Cabianca D. S., Gabellini D., FSHD: copy number variations on the theme of muscular dystrophy Journal of Cell Biology 2010 191 6 1049 1060
-
(2010)
Journal of Cell Biology
, vol.191
, Issue.6
, pp. 1049-1060
-
-
Cabianca, D.S.1
Gabellini, D.2
-
122
-
-
0028040601
-
Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy
-
Hewitt J. E., Lyle R., Clark L. N., Valleley E. M., Wright T. J., Wijmenga C., Van Deutekom J. C. T., Francis F., Sharpe P. T., Hofker M., Frants R. R., Williamson R., Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy Human Molecular Genetics 1994 3 8 1287 1295 (Pubitemid 24255461)
-
(1994)
Human Molecular Genetics
, vol.3
, Issue.8
, pp. 1287-1295
-
-
Hewitt, J.E.1
Lyle, R.2
Clark, L.N.3
Valleley, E.M.4
Wright, T.J.5
Wijmenga, C.6
Van Deutekom, J.C.T.7
Francis, F.8
Sharpe, P.T.9
Hofker, M.10
Frants, R.R.11
Williamson, R.12
-
123
-
-
70450222400
-
Common epigenetic changes of D4Z4 in contraction-dependent and contraction-independent FSHD
-
De Greef J. C., Lemmers R. J., Van Engelen B. G., Sacconi S., Venance S. L., Frants R. R., Tawil R., van der Maarel S. M., Common epigenetic changes of D4Z4 in contraction-dependent and contraction-independent FSHD Human Mutation 2009 30 10 1449 1459
-
(2009)
Human Mutation
, vol.30
, Issue.10
, pp. 1449-1459
-
-
De Greef, J.C.1
Lemmers, R.J.2
Van Engelen, B.G.3
Sacconi, S.4
Venance, S.L.5
Frants, R.R.6
Tawil, R.7
Van Der Maarel, S.M.8
-
124
-
-
0034703873
-
Interchromosomal repeat array interactions between chromosomes 4 and 10: A model for subtelomeric plasticity
-
Van Overveld P. G. M., Lemmers R. J. F. L., Deidda G., Sandkuijl L., Padberg G. W., Frants R. R., Van Der Maarel S. M., Interchromosomal repeat array interactions between chromosomes 4 and 10: a model for subtelomeric plasticity Human Molecular Genetics 2000 9 19 2879 2884
-
(2000)
Human Molecular Genetics
, vol.9
, Issue.19
, pp. 2879-2884
-
-
Van Overveld, P.G.M.1
Lemmers, R.J.F.L.2
Deidda, G.3
Sandkuijl, L.4
Padberg, G.W.5
Frants, R.R.6
Van Der Maarel, S.M.7
-
125
-
-
68249088114
-
Specific loss of histone H3 lysine 9 trimethylation and HP1 /cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD)
-
ARTICLE E1000559
-
Zeng W., De Greef J. C., Chen Y. Y., Chien R., Kong X., Gregson H. C., Winokur S. T., Pyle A., Robertson K. D., Schmiesing J. A., Kimonis V. E., Balog J., Frants R. R., Ball A. R., Lock L. F., Donovan P. J., Van Der Maarel S. M., Yokomori K., Specific loss of histone H3 lysine 9 trimethylation and HP1 /cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD) PLoS Genetics 2009 5 7, article e1000559
-
(2009)
PLoS Genetics
, vol.5
, Issue.7
-
-
Zeng, W.1
De Greef, J.C.2
Chen, Y.Y.3
Chien, R.4
Kong, X.5
Gregson, H.C.6
Winokur, S.T.7
Pyle, A.8
Robertson, K.D.9
Schmiesing, J.A.10
Kimonis, V.E.11
Balog, J.12
Frants, R.R.13
Ball, A.R.14
Lock, L.F.15
Donovan, P.J.16
Van Der Maarel, S.M.17
Yokomori, K.18
-
126
-
-
0037083376
-
Capturing chromosome conformation
-
DOI 10.1126/science.1067799
-
Dekker J., Rippe K., Dekker M., Kleckner N., Capturing chromosome conformation Science 2002 295 5558 1306 1311 (Pubitemid 34157624)
-
(2002)
Science
, vol.295
, Issue.5558
, pp. 1306-1311
-
-
Dekker, J.1
Rippe, K.2
Dekker, M.3
Kleckner, N.4
-
127
-
-
4544273261
-
Localization of 4q35.2 to the nuclear periphery: Is FSHD a nuclear envelope disease?
-
DOI 10.1093/hmg/ddh205
-
Masny P. S., Bengtsson U., Chung S. A., Martin J. H., van Engelen B., van der Maarel S. M., Winokur S. T., Localization of 4q35.2 to the nuclear periphery: is FSHD a nuclear envelope disease? Human Molecular Genetics 2004 13 17 1857 1871 (Pubitemid 39214334)
-
(2004)
Human Molecular Genetics
, vol.13
, Issue.17
, pp. 1857-1871
-
-
Masny, P.S.1
Bengtsson, U.2
Chung, S.-A.3
Martin, J.H.4
Van Engelen, B.5
Van Der Maarel, S.M.6
Winokur, S.T.7
-
128
-
-
7244252921
-
The 4q subtelomere harboring the FSHD locus is specifically anchored with peripheral heterochromatin unlike most human telomeres
-
DOI 10.1083/jcb.200403128
-
Tam R., Smith K. P., Lawrence J. B., The 4q subtelomere harboring the FSHD locus is specifically anchored with peripheral heterochromatin unlike most human telomeres Journal of Cell Biology 2004 167 2 269 279 (Pubitemid 39435070)
-
(2004)
Journal of Cell Biology
, vol.167
, Issue.2
, pp. 269-279
-
-
Tam, R.1
Smith, K.P.2
Lawrence, J.B.3
-
129
-
-
33947575337
-
Evolutionary genomic remodelling of the human 4q subtelomere (4q35.2)
-
Bodega B., Cardone M. F., Mller S., Neusser M., Orzan F., Rossi E., Battaglioli E., Marozzi A., Riva P., Rocchi M., Meneveri R., Ginelli E., Evolutionary genomic remodelling of the human 4q subtelomere (4q35.2) BMC Evolutionary Biology 2007 7, article 39
-
(2007)
BMC Evolutionary Biology
, vol.739
-
-
Bodega, B.1
Cardone, M.F.2
Mller, S.3
Neusser, M.4
Orzan, F.5
Rossi, E.6
Battaglioli, E.7
Marozzi, A.8
Riva, P.9
Rocchi, M.10
Meneveri, R.11
Ginelli, E.12
-
130
-
-
69249208461
-
Identification of a perinuclear positioning element in human subtelomeres that requires A-type lamins and CTCF
-
Ottaviani A., Schluth-Bolard C., Rival-Gervier S., Boussouar A., Rondier D., Foerster A. M., Morere J., Bauwens S., Gazzo S., Callet-Bauchu E., Gilson E., Magdinier F., Identification of a perinuclear positioning element in human subtelomeres that requires A-type lamins and CTCF EMBO Journal 2009 28 16 2428 2436
-
(2009)
EMBO Journal
, vol.28
, Issue.16
, pp. 2428-2436
-
-
Ottaviani, A.1
Schluth-Bolard, C.2
Rival-Gervier, S.3
Boussouar, A.4
Rondier, D.5
Foerster, A.M.6
Morere, J.7
Bauwens, S.8
Gazzo, S.9
Callet-Bauchu, E.10
Gilson, E.11
Magdinier, F.12
-
131
-
-
84859505154
-
Facioscapulohumeral muscular dystrophy: New insights from compound heterozygotes and implication for prenatal genetic counselling
-
Scionti I., Fabbri G., Fiorillo C., Ricci G., Greco F., Facioscapulohumeral muscular dystrophy: new insights from compound heterozygotes and implication for prenatal genetic counselling Journal of Medical Genetics 2012 49 171 178
-
(2012)
Journal of Medical Genetics
, vol.49
, pp. 171-178
-
-
Scionti, I.1
Fabbri, G.2
Fiorillo, C.3
Ricci, G.4
Greco, F.5
-
132
-
-
0014034667
-
The ultrastructure of the nuclear periphery. The Zonula Nucleum Limitans
-
Patrizi G., Poger M., The ultrastructure of the nuclear periphery. The Zonula Nucleum Limitans Journal of Ultrasructure Research 1967 17 1-2 127 136
-
(1967)
Journal of Ultrasructure Research
, vol.17
, Issue.12
, pp. 127-136
-
-
Patrizi, G.1
Poger, M.2
-
133
-
-
0027257461
-
Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C
-
Lin F., Worman H. J., Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C The Journal of Biological Chemistry 1993 268 22 16321 16326 (Pubitemid 23229934)
-
(1993)
Journal of Biological Chemistry
, vol.268
, Issue.22
, pp. 16321-16326
-
-
Lin, F.1
Worman, H.J.2
-
134
-
-
33748760066
-
Farnesylated lamins, progeroid syndromes and farnesyl transferase inhibitors
-
DOI 10.1242/jcs.03156
-
Rusiol A. E., Sinensky M. S., Farnesylated lamins, progeroid syndromes and farnesyl transferase inhibitors Journal of Cell Science 2006 119 16 3265 3272 (Pubitemid 44405212)
-
(2006)
Journal of Cell Science
, vol.119
, Issue.16
, pp. 3265-3272
-
-
Rusinol, A.E.1
Sinensky, M.S.2
-
135
-
-
0024444733
-
The conserved carboxy-terminal cysteine of nuclear lamins is essential for lamin association with the nuclear envelope
-
Krohne G., Waizenegger I., Hoger T. H., The conserved carboxy-terminal cysteine of nuclear lamins is essential for lamin association with the nuclear envelope Journal of Cell Biology 1989 109 5 2003 2011 (Pubitemid 19282589)
-
(1989)
Journal of Cell Biology
, vol.109
, Issue.5
, pp. 2003-2011
-
-
Krohne, G.1
Waizenegger, I.2
Hoger, T.H.3
-
136
-
-
30844434561
-
Prelamin A, Zmpste24, misshapen cell nuclei, and progeria - New evidence suggesting that protein farnesylation could be important for disease pathogenesis
-
DOI 10.1194/jlr.R500011-JLR200
-
Young S. G., Fong L. G., Michaelis S., Prelamin A, Zmpste24, misshapen cell nuclei, and progerianew evidence suggesting that protein farnesylation could be important for disease pathogenesis Journal of Lipid Research 2005 46 12 2531 2558 (Pubitemid 43107466)
-
(2005)
Journal of Lipid Research
, vol.46
, Issue.12
, pp. 2531-2558
-
-
Young, S.G.1
Fong, L.G.2
Michaelis, S.3
-
137
-
-
0030839323
-
A- and B-type lamins are differentially expressed in normal human tissues
-
DOI 10.1007/s004180050138
-
Broers J. L. V., Machiels B. M., Kuijpers H. J. H., Smedts F., Van Den Kieboom R., Raymond Y., Ramaekers F. C. S., A- and B-type lamins are differentially expressed in normal human tissues Histochemistry and Cell Biology 1997 107 6 505 517 (Pubitemid 27306980)
-
(1997)
Histochemistry and Cell Biology
, vol.107
, Issue.6
, pp. 505-517
-
-
Broers, J.L.V.1
Machiels, B.M.2
Kuijpers, H.J.H.3
Smedts, F.4
Van Den Kieboom, R.5
Raymond, Y.6
Ramaekers, F.C.S.7
-
138
-
-
45149084413
-
Domain organization of human chromosomes revealed by mapping of nuclear lamina interactions
-
DOI 10.1038/nature06947, PII NATURE06947
-
Guelen L., Pagie L., Brasset E., Meuleman W., Faza M. B., Talhout W.,
-
(2008)
Nature
, vol.453
, Issue.7197
, pp. 948-951
-
-
Guelen, L.1
Pagie, L.2
Brasset, E.3
Meuleman, W.4
Faza, M.B.5
Talhout, W.6
Eussen, B.H.7
De Klein, A.8
Wessels, L.9
De Laat, W.10
Van Steensel, B.11
-
139
-
-
33748289518
-
Characterization of the Drosophila melanogaster genome at the nuclear lamina
-
DOI 10.1038/ng1852, PII NG1852
-
Pickersgill H., Kalverda B., De Wit E., Talhout W., Fornerod M., Van Steensel B., Characterization of the Drosophila melanogaster genome at the nuclear lamina Nature Genetics 2006 38 9 1005 1014 (Pubitemid 44325925)
-
(2006)
Nature Genetics
, vol.38
, Issue.9
, pp. 1005-1014
-
-
Pickersgill, H.1
Kalverda, B.2
De Wit, E.3
Talhout, W.4
Fornerod, M.5
Van Steensel, B.6
-
140
-
-
33745915850
-
Nuclear lamins: Laminopathies and their role in premature ageing
-
DOI 10.1152/physrev.00047.2005
-
Broers J. L. V., Ramaekers F. C. S., Bonne G., Ben Yaou R., Hutchison C. J., Nuclear lamins: laminopathies and their role in premature ageing Physiological Reviews 2006 86 3 967 1008 (Pubitemid 44042881)
-
(2006)
Physiological Reviews
, vol.86
, Issue.3
, pp. 967-1008
-
-
Broers, J.L.V.1
Ramaekers, F.C.S.2
Bonne, G.3
Ben Yaou, R.4
Hutchison, C.J.5
-
141
-
-
3042829496
-
A-type lamins regulate retinoblastoma protein function by promoting subnuclear localization and preventing proteasomal degradation
-
DOI 10.1073/pnas.0403250101
-
Johnson B. R., Nitta R. T., Frock R. L., Mounkes L., Barbie D. A., Stewart C. L., Harlow E., Kennedy B. K., A-type lamins regulate retinoblastoma protein function by promoting subnuclear localization and preventing proteasomal degradation Proceedings of the National Academy of Sciences of the United States of America 2004 101 26 9677 9682 (Pubitemid 38869295)
-
(2004)
Proceedings of the National Academy of Sciences of the United States of America
, vol.101
, Issue.26
, pp. 9677-9682
-
-
Johnson, B.R.1
Nitta, R.T.2
Frock, R.L.3
Mounkes, L.4
Barbie, D.A.5
Stewart, C.L.6
Harlow, E.7
Kennedy, B.K.8
-
142
-
-
34248391873
-
The nuclear envelope, a key structure in cellular integrity and gene expression
-
DOI 10.2174/092986707780598032
-
Verstraeten V. L. R. M., Broers J. L. V., Ramaekers F. C. S., van Steensel M. A. M., The nuclear envelope, a key structure in cellular integrity and gene expression Current Medicinal Chemistry 2007 14 11 1231 1248 (Pubitemid 46739324)
-
(2007)
Current Medicinal Chemistry
, vol.14
, Issue.11
, pp. 1231-1248
-
-
Verstraeten, V.L.R.M.1
Broers, J.L.V.2
Ramaekers, F.C.S.3
Van Steensel, M.A.M.4
-
143
-
-
52149085911
-
Lamin A/C is a risk biomarker in colorectal cancer
-
ARTICLE E2988
-
Willis N. D., Cox T. R., Rahman-Casas S. F., Smits K., Przyborski S. A., van den Brandt P., van Engeland M., Weijenberg M., Wilson R. G., de Brune A., Hutchison C. J., Lamin A/C is a risk biomarker in colorectal cancer PLoS ONE 2008 3 8, article e2988
-
(2008)
PLoS ONE
, vol.3
, Issue.8
-
-
Willis, N.D.1
Cox, T.R.2
Rahman-Casas, S.F.3
Smits, K.4
Przyborski, S.A.5
Van Den Brandt, P.6
Van Engeland, M.7
Weijenberg, M.8
Wilson, R.G.9
De Brune, A.10
Hutchison, C.J.11
-
144
-
-
0028923173
-
Lamin proteins form an internal nucleoskeleton as well as a peripheral lamina in human cells
-
Hozak P., Sasseville A. M. J., Raymond Y., Cook P. R., Lamin proteins form an internal nucleoskeleton as well as a peripheral lamina in human cells Journal of Cell Science 1995 108 2 635 644
-
(1995)
Journal of Cell Science
, vol.108
, Issue.2
, pp. 635-644
-
-
Hozak, P.1
Sasseville, A.M.J.2
Raymond, Y.3
Cook, P.R.4
-
145
-
-
3142696838
-
Lamin B1 is required for mouse development and nuclear integrity
-
DOI 10.1073/pnas.0401424101
-
Vergnes L., Péterfy M., Bergo M. O., Young S. G., Reue K., Lamin B1 is required for mouse development and nuclear integrity Proceedings of the National Academy of Sciences of the United States of America 2004 101 28 10428 10433 (Pubitemid 38924942)
-
(2004)
Proceedings of the National Academy of Sciences of the United States of America
, vol.101
, Issue.28
, pp. 10428-10433
-
-
Vergnes, L.1
Peterfy, M.2
Bergo, M.O.3
Young, S.G.4
Reue, K.5
-
146
-
-
0033615969
-
Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy
-
Sullivan T., Escalante-Alcalde D., Bhatt H., Anver M., Bhat N., Nagashima K., Stewart C. L., Burke B., Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy Journal of Cell Biology 1999 147 5 913 919
-
(1999)
Journal of Cell Biology
, vol.147
, Issue.5
, pp. 913-919
-
-
Sullivan, T.1
Escalante-Alcalde, D.2
Bhatt, H.3
Anver, M.4
Bhat, N.5
Nagashima, K.6
Stewart, C.L.7
Burke, B.8
-
147
-
-
33845286555
-
Human laminopathies: Nuclei gone genetically awry
-
DOI 10.1038/nrg1906, PII NRG1906
-
Capell B. C., Collins F. S., Human laminopathies: nuclei gone genetically awry Nature Reviews Genetics 2006 7 12 940 952 (Pubitemid 44871397)
-
(2006)
Nature Reviews Genetics
, vol.7
, Issue.12
, pp. 940-952
-
-
Capell, B.C.1
Collins, F.S.2
-
148
-
-
34249742648
-
The position of the mutation within the LMNA gene determines the type and extent of tissue involvement in laminopathies [1]
-
Landires I., Pascale J. M., Motta J., The position of the mutation within the LMNA gene determines the type and extent of tissue involvement in laminopathies [1] Clinical Genetics 2007 71 6 592 596
-
(2007)
Clinical Genetics
, vol.71
, Issue.6
, pp. 592-596
-
-
Landires, I.1
Pascale, J.M.2
Motta, J.3
-
149
-
-
76449114620
-
Genotype-phenotype correlations in laminopathies: How does fate translate?
-
Scharner J., Gnocchi V. F., Ellis J. A., Zammit P. S., Genotype-phenotype correlations in laminopathies: how does fate translate? Biochemical Society Transactions 2010 38 1 257 262
-
(2010)
Biochemical Society Transactions
, vol.38
, Issue.1
, pp. 257-262
-
-
Scharner, J.1
Gnocchi, V.F.2
Ellis, J.A.3
Zammit, P.S.4
-
150
-
-
33745016642
-
Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging
-
DOI 10.1073/pnas.0602569103
-
Shumaker D. K., Dechat T., Kohlmaier A., Adam S. A., Bozovsky M. R., Erdos M. R., Eriksson M., Goldman A. E., Khuon S., Collins F. S., Jenuwein T., Goldman R. D., Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging Proceedings of the National Academy of Sciences of the United States of America 2006 103 23 8703 8708 (Pubitemid 43878083)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, vol.103
, Issue.23
, pp. 8703-8708
-
-
Shumaker, D.K.1
Dechat, T.2
Kohlmaier, A.3
Adam, S.A.4
Bozovsky, M.R.5
Erdos, M.R.6
Eriksson, M.7
Goldman, A.E.8
Khuon, S.9
Collins, F.S.10
Jenuwein, T.11
Goldman, R.D.12
-
151
-
-
33747893889
-
Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery-Dreifuss muscular dystrophy
-
DOI 10.1093/hmg/ddl170
-
Wang Y., Herron A. J., Worman H. J., Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery-Dreifuss muscular dystrophy Human Molecular Genetics 2006 15 16 2479 2489 (Pubitemid 44288701)
-
(2006)
Human Molecular Genetics
, vol.15
, Issue.16
, pp. 2479-2489
-
-
Wang, Y.1
Herron, A.J.2
Worman, H.J.3
-
152
-
-
76149084859
-
Role of A-type lamins in signaling, transcription, and chromatin organization
-
Andrés V., Gonzlez J. M., Role of A-type lamins in signaling, transcription, and chromatin organization Journal of Cell Biology 2009 187 7 945 957
-
(2009)
Journal of Cell Biology
, vol.187
, Issue.7
, pp. 945-957
-
-
Andrés, V.1
Gonzlez, J.M.2
-
153
-
-
67650381905
-
A-type lamins and signaling: The PI 3-kinase/Akt pathway moves forward
-
Marmiroli S., Bertacchini J., Beretti F., Cenni V., Guida M., De Pol A., Maraldi N. M., Lattanzi G., A-type lamins and signaling: the PI 3-kinase/Akt pathway moves forward Journal of Cellular Physiology 2009 220 3 553 564
-
(2009)
Journal of Cellular Physiology
, vol.220
, Issue.3
, pp. 553-564
-
-
Marmiroli, S.1
Bertacchini, J.2
Beretti, F.3
Cenni, V.4
Guida, M.5
De Pol, A.6
Maraldi, N.M.7
Lattanzi, G.8
-
154
-
-
17944376263
-
Class I histone deacetylases sequentially interact with MyoD and pRb during skeletal myogenesis
-
DOI 10.1016/S1097-2765(01)00373-2
-
Puri P. L., Iezzi S., Stiegler P., Chen T. T., Schiltz R. L., Muscat G. E. O., Giordano A., Kedes L., Wang J. Y. J., Sartorelli V., Class I histone deacetylases sequentially interact with MyoD and pRb during skeletal myogenesis Molecular Cell 2001 8 4 885 897 (Pubitemid 33030221)
-
(2001)
Molecular Cell
, vol.8
, Issue.4
, pp. 885-897
-
-
Puri, P.L.1
Iezzi, S.2
Stiegler, P.3
Chen, T.-T.4
Schiltz R.Louis5
Muscat, G.E.O.6
Giordano, A.7
Kedes, L.8
Wang, J.Y.J.9
Sartorelli, V.10
-
155
-
-
26444609690
-
A-type lamins are essential for TGF-β1 induced PP2A to dephosphorylate transcription factors
-
DOI 10.1093/hmg/ddi316
-
Van Berlo J. H., Voncken J. W., Kubben N., Broers J. L. V., Duisters R., van Leeuwen R. E. W., Crijns H. J. G. M., Ramaekers F. C. S., Hutchison C. J., Pinto Y. M., A-type lamins are essential for TGF- 1 induced PP2A to dephosphorylate transcription factors Human Molecular Genetics 2005 14 19 2839 2849 (Pubitemid 41418789)
-
(2005)
Human Molecular Genetics
, vol.14
, Issue.19
, pp. 2839-2849
-
-
Van Berlo, J.H.1
Voncken, J.W.2
Kubben, N.3
Broers, J.L.V.4
Duisters, R.5
Van Leeuwen, R.E.W.6
Crijns, H.J.G.M.7
Ramaekers, F.C.S.8
Hutchison, C.J.9
Pinto, Y.M.10
-
156
-
-
32644447630
-
Lamin A/C and emerin are critical for skeletal muscle satellite cell differentiation
-
DOI 10.1101/gad.1364906
-
Frock R. L., Kudlow B. A., Evans A. M., Jameson S. A., Hauschka S. D., Kennedy B. K., Lamin A/C and emerin are critical for skeletal muscle satellite cell differentiation Genes and Development 2006 20 4 486 500 (Pubitemid 43244402)
-
(2006)
Genes and Development
, vol.20
, Issue.4
, pp. 486-500
-
-
Frock, R.L.1
Kudlow, B.A.2
Evans, A.M.3
Jameson, S.A.4
Hauschka, S.D.5
Kennedy, B.K.6
-
157
-
-
58849128158
-
Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1B
-
Park Y. E., Hayashi Y. K., Goto K., Komaki H., Hayashi Y., Inuzuka T., Noguchi S., Nonaka I., Nishino I., Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1B Neuromuscular Disorders 2009 19 1 29 36
-
(2009)
Neuromuscular Disorders
, vol.19
, Issue.1
, pp. 29-36
-
-
Park, Y.E.1
Hayashi, Y.K.2
Goto, K.3
Komaki, H.4
Hayashi, Y.5
Inuzuka, T.6
Noguchi, S.7
Nonaka, I.8
Nishino, I.9
-
158
-
-
80052693035
-
The Msx1 homeoprotein recruits polycomb to the nuclear periphery during development
-
Wang J., Kumar R. M., Biggs V. J., Lee H., Chen Y., The Msx1 homeoprotein recruits polycomb to the nuclear periphery during development Developmental Cell 2011 21 575 588
-
(2011)
Developmental Cell
, vol.21
, pp. 575-588
-
-
Wang, J.1
Kumar, R.M.2
Biggs, V.J.3
Lee, H.4
Chen, Y.5
-
159
-
-
80054000315
-
An EDMD mutation in C. elegans lamin blocks muscle-specific gene relocation and compromises muscle integrity
-
Mattout A., Pike B. L., Towbin B. D., Bank E. M., Gonzalez-Sandoval A., An EDMD mutation in C. elegans lamin blocks muscle-specific gene relocation and compromises muscle integrity Current Biology 2011 21 19 1603 1614
-
(2011)
Current Biology
, vol.21
, Issue.19
, pp. 1603-1614
-
-
Mattout, A.1
Pike, B.L.2
Towbin, B.D.3
Bank, E.M.4
Gonzalez-Sandoval, A.5
-
160
-
-
56249128582
-
Epigenome: A new target in cancer therapy
-
Giacinti L., Vici P., Lopez M., Epigenome: a new target in cancer therapy Clinica Terapeutica 2008 159 5 347 360
-
(2008)
Clinica Terapeutica
, vol.159
, Issue.5
, pp. 347-360
-
-
Giacinti, L.1
Vici, P.2
Lopez, M.3
-
161
-
-
41149142015
-
Epigenetics and complex disease: From etiology to new therapeutics
-
DOI 10.1146/annurev.pharmtox.48.113006.094731
-
Ptak C., Petronis A., Epigenetics and complex disease: from etiology to new therapeutics Annual Review of Pharmacology and Toxicology 2008 48 257 276 (Pubitemid 351738154)
-
(2008)
Annual Review of Pharmacology and Toxicology
, vol.48
, pp. 257-276
-
-
Ptak, C.1
Petronis, A.2
-
162
-
-
70449711243
-
Computation for ChIP-seq and RNA-seq studies
-
Pepke S., Wold B., Mortazavi A., Computation for ChIP-seq and RNA-seq studies Nature methods 2009 6 11 S22 S32
-
(2009)
Nature Methods
, vol.6
, Issue.11
-
-
Pepke, S.1
Wold, B.2
Mortazavi, A.3
-
163
-
-
61549097508
-
Pharmacoepigenetics and pharmacoepigenomics
-
Peedicayil J., Pharmacoepigenetics and pharmacoepigenomics Pharmacogenomics 2008 9 12 1785 1786
-
(2008)
Pharmacogenomics
, vol.9
, Issue.12
, pp. 1785-1786
-
-
Peedicayil, J.1
-
164
-
-
77953807423
-
Pharmaco-epigenomics: Discovering therapeutic approaches and biomarkers for cancer therapy
-
Claes B., Buysschaert I., Lambrechts D., Pharmaco-epigenomics: discovering therapeutic approaches and biomarkers for cancer therapy Heredity 2010 105 1 152 160
-
(2010)
Heredity
, vol.105
, Issue.1
, pp. 152-160
-
-
Claes, B.1
Buysschaert, I.2
Lambrechts, D.3
|