Brahma-related gene 1 (Brg1) epigenetically regulates CAM activation during hypoxic pulmonary hypertension

Cardiovascular Research

Volumn 100, Issue 3, 2013, Pages 363-373

  Chen, Dewei ^a,b,c   Fang, Fei ^d   Yang, Yuyu ^d   Chen, Jian ^a,b,c   Xu, Gang ^a,b,c   Xu, Yong ^d   Gao, Yuqi ^a,b,c  

^a Key Laboratory of High Altitude Medicine   (China)

^b BEIJING UNIVERSITY OF POSTS AND TELECOMMUNICATIONS   (China)

^c THIRD MILITARY MEDICAL UNIVERSITY   (China)

^d NANJING MEDICAL UNIVERSITY   (China)

Author keywords

Adhesion molecules; Brg1; Epigenetics; Hypoxic pulmonary hypertension; Transcriptional regulation

Indexed keywords

BRG1 PROTEIN; BRM PROTEIN; CELL ADHESION MOLECULE; ENDOTHELIAL LEUKOCYTE ADHESION MOLECULE 1; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; INTERCELLULAR ADHESION MOLECULE 1; VASCULAR CELL ADHESION MOLECULE 1;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL HYPOXIA; CHROMATIN IMMUNOPRECIPITATION; CHROMATIN STRUCTURE; CONTROLLED STUDY; ENDOTHELIAL DYSFUNCTION; ENDOTHELIUM CELL; GENE OVEREXPRESSION; HEART RIGHT VENTRICLE HYPERTROPHY; HISTONE MODIFICATION; HUMAN; HUMAN CELL; IN VITRO STUDY; LEUKOCYTE ADHERENCE; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEPLETION; PULMONARY ARTERY; PULMONARY HYPERTENSION; TRANSACTIVATION; TRANSCRIPTION INITIATION; TRANSCRIPTION REGULATION; UMBILICAL VEIN ENDOTHELIAL CELL; VASCULAR ENDOTHELIUM;

ADHESION MOLECULES; BRG1; EPIGENETICS; HYPOXIC PULMONARY HYPERTENSION; TRANSCRIPTIONAL REGULATION;

ANIMALS; ANOXIA; BINDING SITES; CELL ADHESION; CELL ADHESION MOLECULES; CELL LINE; CHROMATIN ASSEMBLY AND DISASSEMBLY; COCULTURE TECHNIQUES; DISEASE MODELS, ANIMAL; DNA HELICASES; ENDOTHELIAL CELLS; EPIGENESIS, GENETIC; HUMAN UMBILICAL VEIN ENDOTHELIAL CELLS; HUMANS; HYPERTENSION, PULMONARY; LEUKOCYTES; MALE; MICE; MICE, INBRED C57BL; NF-KAPPA B; NUCLEAR PROTEINS; PROMOTER REGIONS, GENETIC; RNA INTERFERENCE; TRANSCRIPTION FACTORS; TRANSCRIPTIONAL ACTIVATION; TRANSFECTION;

EID: 84887877052     PISSN: 00086363     EISSN: 17553245     Source Type: Journal    
DOI: 10.1093/cvr/cvt214     Document Type: Article

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