Functional role of transcriptional factor TBX5 in pre-mRNA splicing and Holt-Oram syndrome via association with SC35

Journal of Biological Chemistry

Volumn 284, Issue 38, 2009, Pages 25653-25663

  Fan, Chun ^a,b   Chen, Qiuyun ^a,b   Wang, Qing Kenneth ^a,b  

^a LERNER RESEARCH INSTITUTE   (United States)

^b HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

AFFINITY PURIFICATION; CARDIAC GENES; CARDIOGENESIS; CO-EXPRESSION; CO-IMMUNOPRECIPITATIONS; COMPLEX FORMATIONS; CONGENITAL HEART DEFECTS; DUAL ROLE; GLUTATHIONE-S-TRANSFERASE; HOMOPOLYMERS; HUMAN DISEASE; LIMB DEVELOPMENT; NOVEL FUNCTIONS; OVER-EXPRESSION; PATHOGENIC MECHANISMS; POSITIVE EFFECTS; PRE-MRNA; PROTEOMICS; PULLDOWN ASSAYS; SPLICE SITE; SPLICING FACTORS; TRANSCRIPTIONAL ACTIVATIONS; TRANSCRIPTIONAL FACTORS; UPPER LIMBS;

BINDING SITES; COBALT COMPOUNDS; MOLECULAR BIOLOGY; NUCLEIC ACIDS; RNA;

SITE SELECTION;

GLUTATHIONE TRANSFERASE; MESSENGER RNA PRECURSOR; TRANSCRIPTION FACTOR TBX5; MULTIPROTEIN COMPLEX; NUCLEAR PROTEIN; RIBONUCLEOPROTEIN; RNA PRECURSOR; SFRS2 PROTEIN, HUMAN; T BOX TRANSCRIPTION FACTOR; T-BOX TRANSCRIPTION FACTOR 5;

ARTICLE; CONTROLLED STUDY; GENE MUTATION; HOLT ORAM SYNDROME; HUMAN; IMMUNOPRECIPITATION; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN FUNCTION; RNA SPLICING; AMINO ACID SUBSTITUTION; CELL LINE; GENETIC DISORDER; GENETICS; METABOLISM; MISSENSE MUTATION; MULTIPLE MALFORMATION SYNDROME; MUTATION; PROTEIN BINDING; TRANSCRIPTION INITIATION;

ABNORMALITIES, MULTIPLE; AMINO ACID SUBSTITUTION; CELL LINE; GENETIC DISEASES, INBORN; HUMANS; MULTIPROTEIN COMPLEXES; MUTATION; MUTATION, MISSENSE; NUCLEAR PROTEINS; PROTEIN BINDING; RIBONUCLEOPROTEINS; RNA PRECURSORS; RNA SPLICE SITES; RNA SPLICING; T-BOX DOMAIN PROTEINS; TRANSCRIPTIONAL ACTIVATION;

EID: 70350025509     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M109.041368     Document Type: Article

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