Williams syndrome is an epigenome-regulator disease

Endocrine Journal

Volumn 58, Issue 2, 2011, Pages 77-85

  Kitagawa, Hirochika ^a,b   Fujiki, Ryoji ^a,c   Yoshimura, Kimihiro ^a,c   Oya, Hiroyuki ^a   Kato, Shigeaki ^a,c  

^a UNIVERSITY OF TOKYO   (Japan)

^b GUNMA UNIVERSITY   (Japan)

^c JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

Chromatin remodeling; Epigenome regulator; VDR; Williams syndrome; WSTF

Indexed keywords

ADENOSINE TRIPHOSPHATASE; CELL NUCLEUS RECEPTOR; MITOGEN ACTIVATED PROTEIN KINASE; MULTIPROTEIN COMPLEX; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG; VITAMIN D RECEPTOR; WILLIAM SYNDROME TRANSCRIPTION FACTOR;

CHROMATIN ASSEMBLY AND DISASSEMBLY; CHROMATIN STRUCTURE; COMPLEX FORMATION; ELECTROLYTE DISTURBANCE; EPIGENETICS; GENE REPRESSION; GENE SWITCHING; GENETIC DISORDER; HEART DISEASE; HUMAN; NONHUMAN; PROTEIN FUNCTION; REVIEW; SIGNAL TRANSDUCTION; TRANSACTIVATION; TRANSCRIPTION REGULATION; WILLIAM SYNDROME;

ADENOSINE TRIPHOSPHATE; ANIMALS; CARDIOVASCULAR ABNORMALITIES; CHROMATIN ASSEMBLY AND DISASSEMBLY; CHROMOSOMES, HUMAN, PAIR 7; EPIGENESIS, GENETIC; GROWTH DISORDERS; HUMANS; HYPERCALCEMIA; MENTAL RETARDATION; MICE; MICE, KNOCKOUT; RECEPTORS, CALCITRIOL; TRANSCRIPTION FACTORS; TRANSCRIPTION, GENETIC; TRANSCRIPTIONAL ACTIVATION; WILLIAMS SYNDROME;

EID: 79952711145     PISSN: 09188959     EISSN: 13484540     Source Type: Journal    
DOI: 10.1507/endocrj.K10E-393     Document Type: Review

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