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Epigenetics
Volumn 7, Issue 11, 2012, Pages 1219-1224
SWI/SNF complex in disorder switching from malignancies to intellectual disability
Author keywords

Cancer; Chromatin remodeling; Coffin siris syndrome; Intellectual disability; SWI SNF
Indexed keywords

EID: 84868344895     PISSN: 15592294     EISSN: 15592308     Source Type: Journal    
DOI: 10.4161/epi.22299     Document Type: Article
Times cited : (70)
References (47)
  • 1
    • 33748367886 scopus 로고    scopus 로고
    • Mammalian SWI/SNF complexes facilitate DNA double-strand break repair by promoting gamma-H2AX induction
    • PMID:16932743
    • Park JH, Park EJ, Lee HS, Kim SJ, Hur SK, Imbalzano AN, et al. Mammalian SWI/SNF complexes facilitate DNA double-strand break repair by promoting gamma-H2AX induction. EMBO J 2006. 25:3986-3997. PMID:16932743. http://dx.doi.org/10.1038/sj.emboj.7601291.
    • (2006) EMBO J , vol.25 , pp. 3986-3997
    • Park, J.H.1    Park, E.J.2    Lee, H.S.3    Kim, S.J.4    Hur, S.K.5    Imbalzano, A.N.6
  • 2
    • 79959653996 scopus 로고    scopus 로고
    • SWI/SNF nucleosome remodellers and cancer
    • PMID:21654818
    • Wilson BG, Roberts CW. SWI/SNF nucleosome remodellers and cancer. Nat Rev Cancer 2011. 11:481-492. PMID:21654818. http://dx.doi.org/10.1038/nrc3068.
    • (2011) Nat Rev Cancer , vol.11 , pp. 481-492
    • Wilson, B.G.1    Roberts, C.W.2
  • 3
    • 34548526743 scopus 로고    scopus 로고
    • Chromatin remodeling and cancer, Part I: Covalent histone modifications
    • PMID:17822958
    • Wang GG, Allis CD, Chi P. Chromatin remodeling and cancer, Part I: Covalent histone modifications. Trends Mol Med 2007. 13:363-372. PMID:17822958. http://dx.doi.org/10.1016/j.molmed.2007.07.003.
    • (2007) Trends Mol Med , vol.13 , pp. 363-372
    • Wang, G.G.1    Allis, C.D.2    Chi, P.3
  • 4
    • 34548544648 scopus 로고    scopus 로고
    • Chromatin remodeling and cancer, Part II: ATP-dependent chromatin remodeling
    • PMID:17822959
    • Wang GG, Allis CD, Chi P. Chromatin remodeling and cancer, Part II: ATP-dependent chromatin remodeling. Trends Mol Med 2007. 13:373-380. PMID:17822959. http://dx.doi.org/10.1016/j.molmed.2007.07.004.
    • (2007) Trends Mol Med , vol.13 , pp. 373-380
    • Wang, G.G.1    Allis, C.D.2    Chi, P.3
  • 5
    • 79952539053 scopus 로고    scopus 로고
    • ATP-dependent chromatin remodeling: Genetics, genomics and mechanisms
    • PMID:21358755
    • Hargreaves DC, Crabtree GR. ATP-dependent chromatin remodeling: genetics, genomics and mechanisms. Cell Res 2011. 21:396-420. PMID:21358755. http://dx.doi.org/10.1038/cr.2011.32.
    • (2011) Cell Res , vol.21 , pp. 396-420
    • Hargreaves, D.C.1    Crabtree, G.R.2
  • 6
    • 49449108027 scopus 로고    scopus 로고
    • Fission yeast SWI/SNF and RSC complexes show compositional and functional differences from budding yeast
    • PMID:18622392
    • Monahan BJ, Villén J, Marguerat S, Bähler J, Gygi SP, Winston F. Fission yeast SWI/SNF and RSC complexes show compositional and functional differences from budding yeast. Nat Struct Mol Biol 2008. 15:873-880. PMID:18622392. http://dx.doi.org/10.1038/nsmb.1452.
    • (2008) Nat Struct Mol Biol , vol.15 , pp. 873-880
    • Monahan, B.J.1    Villén, J.2    Marguerat, S.3    Bähler, J.4    Gygi, S.P.5    Winston, F.6
  • 7
    • 65249173999 scopus 로고    scopus 로고
    • An embryonic stem cell chromatin remodeling complex, esBAF, is an essential component of the core pluripotency transcriptional network
    • PMID:19279218
    • Ho L, Jothi R, Ronan JL, Cui K, Zhao K, Crabtree GR. An embryonic stem cell chromatin remodeling complex, esBAF, is an essential component of the core pluripotency transcriptional network. Proc Natl Acad Sci U S A 2009. 106:5187-5191. PMID:19279218. http://dx.doi.org/10.1073/pnas.0812888106.
    • (2009) Proc Natl Acad Sci U S A , vol.106 , pp. 5187-5191
    • Ho, L.1    Jothi, R.2    Ronan, J.L.3    Cui, K.4    Zhao, K.5    Crabtree, G.R.6
  • 8
    • 33846977688 scopus 로고    scopus 로고
    • Distinct mammalian SWI/SNF chromatin remodeling complexes with opposing roles in cell-cycle control
    • PMID:17255939
    • Nagl NG Jr., Wang X, Patsialou A, Van Scoy M, Moran E. Distinct mammalian SWI/SNF chromatin remodeling complexes with opposing roles in cell-cycle control. EMBO J 2007. 26:752-763. PMID:17255939. http://dx.doi.org/10.1038/sj.emboj.7601541.
    • (2007) EMBO J , vol.26 , pp. 752-763
    • Nagl Jr., N.G.1    Wang, X.2    Patsialou, A.3    van Scoy, M.4    Moran, E.5
  • 9
    • 76049106059 scopus 로고    scopus 로고
    • Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome
    • PMID:20137775
    • Schneppenheim R, Frühwald MC, Gesk S, Hasselblatt M, Jeibmann A, Kordes U, et al. Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome. Am J Hum Genet 2010. 86:279-284. PMID:20137775. http://dx.doi.org/10.1016/j.ajhg.2010.01.013.
    • (2010) Am J Hum Genet , vol.86 , pp. 279-284
    • Schneppenheim, R.1    Frühwald, M.C.2    Gesk, S.3    Hasselblatt, M.4    Jeibmann, A.5    Kordes, U.6
  • 10
    • 84862811132 scopus 로고    scopus 로고
    • Frequency of SMARCB1 mutations in familial and sporadic schwannomatosis
    • PMID:22434358
    • Smith MJ, Wallace AJ, Bowers NL, Rustad CF, Woods CG, Leschziner GD, et al. Frequency of SMARCB1 mutations in familial and sporadic schwannomatosis. Neurogenetics 2012. 13:141-145. PMID:22434358. http://dx.doi.org/10.1007/s10048-012-0319-8.
    • (2012) Neurogenetics , vol.13 , pp. 141-145
    • Smith, M.J.1    Wallace, A.J.2    Bowers, N.L.3    Rustad, C.F.4    Woods, C.G.5    Leschziner, G.D.6
  • 11
    • 0034610395 scopus 로고    scopus 로고
    • Haploinsufficiency of Snf5 (integrase interactor 1) predisposes to malignant rhabdoid tumors in mice
    • PMID:11095756
    • Roberts CW, Galusha SA, McMenamin ME, Fletcher CD, Orkin SH. Haploinsufficiency of Snf5 (integrase interactor 1) predisposes to malignant rhabdoid tumors in mice. Proc Natl Acad Sci U S A 2000. 97:13796-13800. PMID:11095756. http://dx.doi.org/10.1073/pnas.250492697.
    • (2000) Proc Natl Acad Sci U S A , vol.97 , pp. 13796-13800
    • Roberts, C.W.1    Galusha, S.A.2    McMenamin, M.E.3    Fletcher, C.D.4    Orkin, S.H.5
  • 12
    • 0034502484 scopus 로고    scopus 로고
    • A Brg1 null mutation in the mouse reveals functional differences among mammalian SWI/SNF complexes
    • PMID:11163203
    • Bultman S, Gebuhr T, Yee D, La Mantia C, Nicholson J, Gilliam A, et al. A Brg1 null mutation in the mouse reveals functional differences among mammalian SWI/SNF complexes. Mol Cell 2000. 6:1287-1295. PMID:11163203. http://dx.doi.org/10.1016/S1097-2765(00)00127-1.
    • (2000) Mol Cell , vol.6 , pp. 1287-1295
    • Bultman, S.1    Gebuhr, T.2    Yee, D.3    la Mantia, C.4    Nicholson, J.5    Gilliam, A.6
  • 13
    • 0034572885 scopus 로고    scopus 로고
    • The murine SNF5/INI1 chromatin remodeling factor is essential for embryonic development and tumor suppression
    • PMID:11263494
    • Klochendler-Yeivin A, Fiette L, Barra J, Muchardt C, Babinet C, Yaniv M. The murine SNF5/INI1 chromatin remodeling factor is essential for embryonic development and tumor suppression. EMBO Rep 2000. 1:500-506. PMID:11263494.
    • (2000) EMBO Rep , vol.1 , pp. 500-506
    • Klochendler-Yeivin, A.1    Fiette, L.2    Barra, J.3    Muchardt, C.4    Babinet, C.5    Yaniv, M.6
  • 14
    • 84865071031 scopus 로고    scopus 로고
    • Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B
    • PMID:21801163
    • Halgren C, Kjaergaard S, Bak M, Hansen C, El-Schich Z, Anderson C, et al. Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B. Clin Genet 2011. 82: 248-255. PMID:21801163. http://dx.doi.org/10.1111/j.1399-0004.2011.01755.x.
    • (2011) Clin Genet , vol.82 , pp. 248-255
    • Halgren, C.1    Kjaergaard, S.2    Bak, M.3    Hansen, C.4    El-Schich, Z.5    Anderson, C.6
  • 15
    • 78651098091 scopus 로고    scopus 로고
    • A balanced translocation t(6.14) (q25.3.q13.2) leading to reciprocal fusion transcripts in a patient with intellectual disability and agenesis of corpus callosum
    • PMID:21042007
    • Backx L, Seuntjens E, Devriendt K, Vermeesch J, van Esch H. A balanced translocation t(6.14) (q25.3.q13.2) leading to reciprocal fusion transcripts in a patient with intellectual disability and agenesis of corpus callosum. Cytogenet Genome Res 2011. 132:135-143. PMID:21042007. http://dx.doi.org/10.1159/000321577.
    • (2011) Cytogenet Genome Res , vol.132 , pp. 135-143
    • Backx, L.1    Seuntjens, E.2    Devriendt, K.3    Vermeesch, J.4    van Esch, H.5
  • 16
    • 84858021960 scopus 로고    scopus 로고
    • Haploinsufficiency of ARID1B, a member of the SWI/SNF-a chromatin-remodeling complex, is a frequent cause of intellectual disability
    • PMID:22405089
    • Hoyer J, Ekici AB, Endele S, Popp B, Zweier C, Wiesener A, et al. Haploinsufficiency of ARID1B, a member of the SWI/SNF-a chromatin-remodeling complex, is a frequent cause of intellectual disability. Am J Hum Genet 2012. 90:565-572. PMID:22405089. http://dx.doi.org/10.1016/j.ajhg.2012.02.007.
    • (2012) Am J Hum Genet , vol.90 , pp. 565-572
    • Hoyer, J.1    Ekici, A.B.2    Endele, S.3    Popp, B.4    Zweier, C.5    Wiesener, A.6
  • 17
    • 84862830331 scopus 로고    scopus 로고
    • Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome
    • PMID:22426309
    • Santen GW, Aten E, Sun Y, Almomani R, Gilissen C, Nielsen M, et al. Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome. Nat Genet 2012. 44:379-380. PMID:22426309. http://dx.doi.org/10.1038/ng.2217.
    • (2012) Nat Genet , vol.44 , pp. 379-380
    • Santen, G.W.1    Aten, E.2    Sun, Y.3    Almomani, R.4    Gilissen, C.5    Nielsen, M.6
  • 18
    • 84859427243 scopus 로고    scopus 로고
    • Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome
    • PMID:22426308
    • Tsurusaki Y, Okamoto N, Ohashi H, Kosho T, Imai Y, Hibi-Ko Y, et al. Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome. Nat Genet 2012. 44:376-378. PMID:22426308. http://dx.doi.org/10.1038/ng.2219.
    • (2012) Nat Genet , vol.44 , pp. 376-378
    • Tsurusaki, Y.1    Okamoto, N.2    Ohashi, H.3    Kosho, T.4    Imai, Y.5    Hibi-Ko, Y.6
  • 19
    • 84859423484 scopus 로고    scopus 로고
    • Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome
    • PMID:22366787
    • Van Houdt JK, Nowakowska BA, Sousa SB, van Schaik BD, Seuntjens E, Avonce N, et al. Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome. Nat Genet 2012. 44:445-449+S1. PMID:22366787. http://dx.doi.org/10.1038/ng.1105.
    • (2012) Nat Genet , vol.44
    • van Houdt, J.K.1    Nowakowska, B.A.2    Sousa, S.B.3    van Schaik, B.D.4    Seuntjens, E.5    Avonce, N.6
  • 20
    • 84860338936 scopus 로고    scopus 로고
    • In-frame deletion and missense mutations of the C-terminal Helicase domain of SMARCA2 in three patients with Nicolaides-Baraitser syndrome
    • PMID:22822383
    • Wolff D, Endele S, Azzarello-Burri S, Hoyer J, Zweier M, Schanze I, et al. In-frame deletion and missense mutations of the C-terminal Helicase domain of SMARCA2 in three patients with Nicolaides-Baraitser syndrome. Mol Syndromol 2012. 2:237-244. PMID:22822383.
    • (2012) Mol Syndromol , vol.2 , pp. 237-244
    • Wolff, D.1    Endele, S.2    Azzarello-Burri, S.3    Hoyer, J.4    Zweier, M.5    Schanze, I.6
  • 21
    • 84861576201 scopus 로고    scopus 로고
    • Oslo Breast Cancer Consortium (OSBREAC). The landscape of cancer genes and mutational processes in breast cancer
    • PMID:22722201
    • Stephens PJ, Tarpey PS, Davies H, Van Loo P, Greenman C, Wedge DC, et al. Oslo Breast Cancer Consortium (OSBREAC). The landscape of cancer genes and mutational processes in breast cancer. Nature 2012. 486:400-404. PMID:22722201.
    • (2012) Nature , vol.486 , pp. 400-404
    • Stephens, P.J.1    Tarpey, P.S.2    Davies, H.3    van Loo, P.4    Greenman, C.5    Wedge, D.C.6
  • 22
    • 84860327480 scopus 로고    scopus 로고
    • Exome sequencing of gastric adenocarcinoma identifies recurrent somatic mutations in cell adhesion and chromatin remodeling genes
    • PMID:22484628
    • Zang ZJ, Cutcutache I, Poon SL, Zhang SL, McPherson JR, Tao J, et al. Exome sequencing of gastric adenocarcinoma identifies recurrent somatic mutations in cell adhesion and chromatin remodeling genes. Nat Genet 2012. 44:570-574. PMID:22484628. http://dx.doi.org/10.1038/ng.2246.
    • (2012) Nat Genet , vol.44 , pp. 570-574
    • Zang, Z.J.1    Cutcutache, I.2    Poon, S.L.3    Zhang, S.L.4    McPherson, J.R.5    Tao, J.6
  • 23
    • 84861840669 scopus 로고    scopus 로고
    • Loss of ARID1A/ BAF250a-expression in endometriosis: A biomarker for risk of carcinogenic transformation?
    • PMID:22301703
    • Samartzis EP, Samartzis N, Noske A, Fedier A, Caduff R, Dedes KJ, et al. Loss of ARID1A/ BAF250a-expression in endometriosis: a biomarker for risk of carcinogenic transformation? Mod Pathol 2012. 25:885-892. PMID:22301703. http://dx.doi.org/10.1038/modpathol.2011.217.
    • (2012) Mod Pathol , vol.25 , pp. 885-892
    • Samartzis, E.P.1    Samartzis, N.2    Noske, A.3    Fedier, A.4    Caduff, R.5    Dedes, K.J.6
  • 24
    • 7444246651 scopus 로고    scopus 로고
    • Two related ARID family proteins are alternative subunits of human SWI/SNF complexes
    • PMID:15170388
    • Wang X, Nagl NG, Wilsker D, Van Scoy M, Pacchione S, Yaciuk P, et al. Two related ARID family proteins are alternative subunits of human SWI/SNF complexes. Biochem J 2004. 383:319-325. PMID:15170388. http://dx.doi.org/10.1042/BJ20040524.
    • (2004) Biochem J , vol.383 , pp. 319-325
    • Wang, X.1    Nagl, N.G.2    Wilsker, D.3    van Scoy, M.4    Pacchione, S.5    Yaciuk, P.6
  • 25
    • 79960270597 scopus 로고    scopus 로고
    • Dynamics of expression of ARID1A and ARID1B subunits in mouse embryos and in cells during the cell cycle
    • PMID:21647563
    • Flores-Alcantar A, Gonzalez-Sandoval A, Escalante-Alcalde D, Lomelí H. Dynamics of expression of ARID1A and ARID1B subunits in mouse embryos and in cells during the cell cycle. Cell Tissue Res 2011. 345:137-148. PMID:21647563. http://dx.doi.org/10.1007/s00441-011-1182-x.
    • (2011) Cell Tissue Res , vol.345 , pp. 137-148
    • Flores-Alcantar, A.1    Gonzalez-Sandoval, A.2    Escalante-Alcalde, D.3    Lomelí, H.4
  • 26
    • 2042432488 scopus 로고    scopus 로고
    • Constitutional mutations of the hSNF5/INI1 gene predispose to a variety of cancers
    • PMID:10521299
    • Sévenet N, Sheridan E, Amram D, Schneider P, Handgretinger R, Delattre O. Constitutional mutations of the hSNF5/INI1 gene predispose to a variety of cancers. Am J Hum Genet 1999. 65:1342-1348. PMID:10521299. http://dx.doi.org/10.1086/302639.
    • (1999) Am J Hum Genet , vol.65 , pp. 1342-1348
    • Sévenet, N.1    Sheridan, E.2    Amram, D.3    Schneider, P.4    Handgretinger, R.5    Delattre, O.6
  • 27
    • 84864444165 scopus 로고    scopus 로고
    • Novel mutations target distinct subgroups of medulloblastoma
    • PMID:22722829
    • Robinson G, Parker M, Kranenburg TA, Lu C, Chen X, Ding L, et al. Novel mutations target distinct subgroups of medulloblastoma. Nature 2012. 488:43-48. PMID:22722829. http://dx.doi.org/10.1038/nature11213.
    • (2012) Nature , vol.488 , pp. 43-48
    • Robinson, G.1    Parker, M.2    Kranenburg, T.A.3    Lu, C.4    Chen, X.5    Ding, L.6
  • 28
    • 84860833500 scopus 로고    scopus 로고
    • Reorganizing the protein space at the Universal Protein Resource (UniProt)
    • UniProt Consortium, PMID:22102590
    • UniProt Consortium. Reorganizing the protein space at the Universal Protein Resource (UniProt). Nucleic Acids Res 2012. 40:D71-D75. PMID:22102590. http://dx.doi.org/10.1093/nar/gkr981.
    • (2012) Nucleic Acids Res , vol.40
  • 29
    • 0034973588 scopus 로고    scopus 로고
    • Essential roles of Snf5p in Snf-Swi chromatin remodeling in vivo
    • PMID:11390659
    • Geng F, Cao Y, Laurent BC. Essential roles of Snf5p in Snf-Swi chromatin remodeling in vivo. Mol Cell Biol 2001. 21:4311-4320. PMID:11390659. http://dx.doi.org/10.1128/MCB.21.13.4311-4320.2001.
    • (2001) Mol Cell Biol , vol.21 , pp. 4311-4320
    • Geng, F.1    Cao, Y.2    Laurent, B.C.3
  • 30
    • 0035147417 scopus 로고    scopus 로고
    • INI1 mutations in meningiomas at a potential hotspot in exon 9
    • PMID:11161377
    • Schmitz U, Mueller W, Weber M, Sévenet N, Delattre O, von Deimling A. INI1 mutations in meningiomas at a potential hotspot in exon 9. Br J Cancer 2001. 84:199-201. PMID:11161377. http://dx.doi.org/10.1054/bjoc.2000.1583.
    • (2001) Br J Cancer , vol.84 , pp. 199-201
    • Schmitz, U.1    Mueller, W.2    Weber, M.3    Sévenet, N.4    Delattre, O.5    von Deimling, A.6
  • 31
    • 34548549334 scopus 로고    scopus 로고
    • The HMGbox: A versatile protein domain occurring in a wide variety of DNA-binding proteins
    • PMID:17599239
    • Stros M, Launholt D, Grasser KD. The HMGbox: a versatile protein domain occurring in a wide variety of DNA-binding proteins. Cell Mol Life Sci 2007. 64:2590-2606. PMID:17599239. http://dx.doi.org/10.1007/s00018-007-7162-3.
    • (2007) Cell Mol Life Sci , vol.64 , pp. 2590-2606
    • Stros, M.1    Launholt, D.2    Grasser, K.D.3
  • 32
    • 79960846717 scopus 로고    scopus 로고
    • Identification and characterization of novel potentially oncogenic mutations in the human BAF57 gene in a breast cancer patient
    • PMID:21465167
    • Villaronga MA, López-Mateo I, Markert L, Espinosa E, Fresno Vara JA, Belandia B. Identification and characterization of novel potentially oncogenic mutations in the human BAF57 gene in a breast cancer patient. Breast Cancer Res Treat 2011. 128:891-898. PMID:21465167. http://dx.doi.org/10.1007/s10549-011-1492-1494.
    • (2011) Breast Cancer Res Treat , vol.128 , pp. 891-898
    • Villaronga, M.A.1    López-Mateo, I.2    Markert, L.3    Espinosa, E.4    Fresno, V.J.A.5    Belandia, B.6
  • 33
    • 34447249019 scopus 로고    scopus 로고
    • An essential switch in subunit composition of a chromatin remodeling complex during neural development
    • PMID:17640523
    • Lessard J, Wu JI, Ranish JA, Wan M, Winslow MM, Staahl BT, et al. An essential switch in subunit composition of a chromatin remodeling complex during neural development. Neuron 2007. 55:201-215. PMID:17640523. http://dx.doi.org/10.1016/j.neuron.2007.06.019.
    • (2007) Neuron , vol.55 , pp. 201-215
    • Lessard, J.1    Wu, J.I.2    Ranish, J.A.3    Wan, M.4    Winslow, M.M.5    Staahl, B.T.6
  • 34
    • 80052838640 scopus 로고    scopus 로고
    • Unlocking Mendelian disease using exome sequencing
    • PMID:21920049
    • Gilissen C, Hoischen A, Brunner HG, Veltman JA. Unlocking Mendelian disease using exome sequencing. Genome Biol 2011. 12:228. PMID:21920049. http://dx.doi.org/10.1186/gb-2011-12-9-228.
    • (2011) Genome Biol , vol.12 , pp. 228
    • Gilissen, C.1    Hoischen, A.2    Brunner, H.G.3    Veltman, J.A.4
  • 36
    • 18544384537 scopus 로고    scopus 로고
    • Haploinsufficiency of NSD1 causes Sotos syndrome
    • PMID:11896389
    • Kurotaki N, Imaizumi K, Harada N, Masuno M, Kondoh T, Nagai T, et al. Haploinsufficiency of NSD1 causes Sotos syndrome. Nat Genet 2002. 30:365-366. PMID:11896389. http://dx.doi.org/10.1038/ng863.
    • (2002) Nat Genet , vol.30 , pp. 365-366
    • Kurotaki, N.1    Imaizumi, K.2    Harada, N.3    Masuno, M.4    Kondoh, T.5    Nagai, T.6
  • 37
    • 84855825406 scopus 로고    scopus 로고
    • FORGE Canada Consortium. Mutations in EZH2 cause Weaver syndrome
    • PMID:22177091
    • Gibson WT, Hood RL, Zhan SH, Bulman DE, Fejes AP, Moore R, et al. FORGE Canada Consortium. Mutations in EZH2 cause Weaver syndrome. Am J Hum Genet 2012. 90:110-118. PMID:22177091. http://dx.doi.org/10.1016/j.ajhg.2011.11.018.
    • (2012) Am J Hum Genet , vol.90 , pp. 110-118
    • Gibson, W.T.1    Hood, R.L.2    Zhan, S.H.3    Bulman, D.E.4    Fejes, A.P.5    Moore, R.6
  • 38
    • 84863795741 scopus 로고    scopus 로고
    • Childhood Overgrowth Collaboration. Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height
    • PMID:22190405
    • Tatton-Brown K, Hanks S, Ruark E, Zachariou A, Duarte Sdel V, Ramsay E, et al. Childhood Overgrowth Collaboration. Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height. Oncotarget 2011. 2:1127-1133. PMID:22190405.
    • (2011) Oncotarget , vol.2 , pp. 1127-1133
    • Tatton-Brown, K.1    Hanks, S.2    Ruark, E.3    Zachariou, A.4    Duarte, S.V.5    Ramsay, E.6
  • 39
    • 84863217444 scopus 로고    scopus 로고
    • Histone modification defects in developmental disorders and cancer
    • PMID:22287508
    • Cross NC. Histone modification defects in developmental disorders and cancer. Oncotarget 2012. 3:3-4. PMID:22287508.
    • (2012) Oncotarget , vol.3 , pp. 3-4
    • Cross, N.C.1
  • 40
    • 77953140591 scopus 로고    scopus 로고
    • A role for BAF57 in cell cycledependent transcriptional regulation by the SWI/SNF chromatin remodeling complex
    • PMID:20460533
    • Hah N, Kolkman A, Ruhl DD, Pijnappel WW, Heck AJ, Timmers HT, et al. A role for BAF57 in cell cycledependent transcriptional regulation by the SWI/SNF chromatin remodeling complex. Cancer Res 2010. 70:4402-4411. PMID:20460533. http://dx.doi.org/10.1158/0008-5472.CAN-09-2767.
    • (2010) Cancer Res , vol.70 , pp. 4402-4411
    • Hah, N.1    Kolkman, A.2    Ruhl, D.D.3    Pijnappel, W.W.4    Heck, A.J.5    Timmers, H.T.6
  • 41
    • 84862785757 scopus 로고    scopus 로고
    • SRG3/mBAF155 stabilizes the SWI/SNF-like BAF complex by blocking CHFR mediated ubiquitination and degradation of its major components
    • PMID:22285184
    • Jung I, Sohn DH, Choi J, Kim JM, Jeon S, Seol JH, et al. SRG3/mBAF155 stabilizes the SWI/SNF-like BAF complex by blocking CHFR mediated ubiquitination and degradation of its major components. Biochem Biophys Res Commun 2012. 418:512-517. PMID:22285184. http://dx.doi.org/10.1016/j.bbrc.2012.01.057.
    • (2012) Biochem Biophys Res Commun , vol.418 , pp. 512-517
    • Jung, I.1    Sohn, D.H.2    Choi, J.3    Kim, J.M.4    Jeon, S.5    Seol, J.H.6
  • 42
    • 83255184470 scopus 로고    scopus 로고
    • Identification of a core member of the SWI/SNF complex, BAF155/SMARCC1, as a human tumor suppressor gene
    • PMID:22139574
    • DelBove J, Rosson G, Strobeck M, Chen J, Archer TK, Wang W, et al. Identification of a core member of the SWI/SNF complex, BAF155/SMARCC1, as a human tumor suppressor gene. Epigenetics 2011. 6:1444-1453. PMID:22139574. http://dx.doi.org/10.4161/epi.6.12.18492.
    • (2011) Epigenetics , vol.6 , pp. 1444-1453
    • Delbove, J.1    Rosson, G.2    Strobeck, M.3    Chen, J.4    Archer, T.K.5    Wang, W.6
  • 43
    • 84858602406 scopus 로고    scopus 로고
    • InterPro in 2011: New developments in the family and domain prediction database
    • (Database issue), PMID:22096229
    • Hunter S, Jones P, Mitchell A, Apweiler R, Attwood TK, Bateman A, et al. InterPro in 2011: new developments in the family and domain prediction database. Nucleic Acids Res 2012. 40(Database issue):D306-D312. PMID:22096229. http://dx.doi.org/10.1093/nar/gkr948.
    • (2012) Nucleic Acids Res , vol.40
    • Hunter, S.1    Jones, P.2    Mitchell, A.3    Apweiler, R.4    Attwood, T.K.5    Bateman, A.6
  • 44
    • 0347752388 scopus 로고    scopus 로고
    • GeneNote: Whole genome expression profiles in normal human tissues
    • PMID:14744114
    • Shmueli O, Horn-Saban S, Chalifa-Caspi V, Shmoish M, Ophir R, Benjamin-Rodrig H, et al. GeneNote: whole genome expression profiles in normal human tissues. C R Biol 2003. 326:1067-1072. PMID:14744114. http://dx.doi.org/10.1016/j.crvi.2003.09.012.
    • (2003) C R Biol , vol.326 , pp. 1067-1072
    • Shmueli, O.1    Horn-Saban, S.2    Chalifa-Caspi, V.3    Shmoish, M.4    Ophir, R.5    Benjamin-Rodrig, H.6
  • 45
    • 80155131218 scopus 로고    scopus 로고
    • ARID1A, a factor that promotes formation of SWI/SNF-mediated chromatin remodeling, is a tumor suppressor in gynecologic cancers
    • PMID:21900401
    • Guan B, Wang TL, Shih IeM. ARID1A, a factor that promotes formation of SWI/SNF-mediated chromatin remodeling, is a tumor suppressor in gynecologic cancers. Cancer Res 2011. 71:6718-6727. PMID:21900401. http://dx.doi.org/10.1158/0008-5472.CAN-11-1562.
    • (2011) Cancer Res , vol.71 , pp. 6718-6727
    • Guan, B.1    Wang, T.L.2    Shih, I.3
  • 46
    • 82255183148 scopus 로고    scopus 로고
    • Exome sequencing identifies frequent mutation of ARID1A in molecular subtypes of gastric cancer
    • PMID:22037554
    • Wang K, Kan J, Yuen ST, Shi ST, Chu KM, Law S, et al. Exome sequencing identifies frequent mutation of ARID1A in molecular subtypes of gastric cancer. Nat Genet 2011. 43:1219-1223. PMID:22037554. http://dx.doi.org/10.1038/ng.982.
    • (2011) Nat Genet , vol.43 , pp. 1219-1223
    • Wang, K.1    Kan, J.2    Yuen, S.T.3    Shi, S.T.4    Chu, K.M.5    Law, S.6
  • 47
    • 77957946398 scopus 로고    scopus 로고
    • ARID1A mutations in endometriosisassociated ovarian carcinomas
    • PMID:20942669
    • Wiegand KC, Shah SP, Al-Agha OM, Zhao Y, Tse K, Zeng T, et al. ARID1A mutations in endometriosisassociated ovarian carcinomas. N Engl J Med 2010. 363:1532-1543. PMID:20942669. http://dx.doi.org/10.1056/NEJMoa1008433.
    • (2010) N Engl J Med , vol.363 , pp. 1532-1543
    • Wiegand, K.C.1    Shah, S.P.2    Al-Agha, O.M.3    Zhao, Y.4    Tse, K.5    Zeng, T.6

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