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299409 occurrences (No.76 in the rank) during 5 years in the PubMed. [no cache] 500 found

303) Our understanding of congenital heart defects has been recently advanced by whole exome sequencing projects, which have identified de novo mutations in many genes encoding epigenetic regulators.

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PMID:24183004 DOI:10.1016/j.carpath.2013.09.003

2015 Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology

* SWI/SNF chromatin-remodeling complexes in cardiovascular development and disease.

- Our understanding of congenital heart defects has been recently advanced by whole exome sequencing projects, which have identified de novo mutations in many genes encoding epigenetic regulators. Notably, multiple subunits of switching defective/sucrose non-fermenting (SWI/SNF) chromatin-remodeling complexes have been identified as strong candidates underlying these defects because they physically and functionally interact with cardiogenic transcription factors critical to cardiac development, such as TBX5, GATA-4, and NKX2-5. While these studies indicate a critical role of SWI/SNF complexes in cardiac development and congenital heart disease, many exciting new discoveries have identified their critical role in the adult heart in both physiological and pathological conditions involving multiple cell types in the heart, including cardiomyocytes, vascular endothelial cells, pericytes, and neural crest cells. This review summarizes the role of SWI/SNF chromatin-remodeling complexes in cardiac development, congenital heart disease, cardiac hypertrophy, and vascular endothelial cell survival. Although the clinical relevance of SWI/SNF mutations has traditionally been focused primarily on their role in tumor suppression, these recent studies illustrate their critical role in the heart whereby they regulate cell proliferation, differentiation, and apoptosis of cardiac derived cell lines.

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(1)101 and	(12)8 including	(23)4 for	(34)2 13
(2)36 null	(13)7 encoding	(24)4 from	(35)2 but
(3)28 are	(14)7 involved	(25)4 related	(36)2 can
(4)26 were	(15)7 which	(26)4 with	(37)2 coding
(5)25 in	(16)6 (PCGs),	(27)3 had	(38)2 expressed
(6)16 2	(17)6 use	(28)3 have	(39)2 is
(7)14 (13	(18)5 may	(29)3 stop	(40)2 on
(8)14 22	(19)5 that	(30)3 such	(41)2 ranged
(9)12 start	(20)4 (PCGs)	(31)2 (cytb,	(42)2 to
(10)11 of	(21)4 as	(32)2 (pnad1
(11)9 was	(22)4 associated	(33)2 (srfAA,

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--- WordNet output for genes --- =>発生, 起源, 起こり, 生成, 創始, 創世記 Overview of noun gene The noun gene has 1 sense (no senses from tagged texts) 1. gene, cistron, factor -- ((genetics) a segment of DNA that is involved in producing a polypeptide chain; it can include regions preceding and following the coding DNA as well as introns between the exons; it is considered a unit of heredity; "genes were formerly called factors") --- WordNet end ---