Characterization of the TBX5 binding site and analysis of mutations that cause Holt-Oram syndrome

Human Molecular Genetics

Volumn 10, Issue 18, 2001, Pages 1983-1994

  Ghosh, T K ^a   Packham, E A ^a   Bonser, A J ^a   Robinson, T E ^a   Cross, S J ^a   Brook, J D ^a  

^a UNIVERSITY OF NOTTINGHAM   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA ACTIN; AMINO ACID; ATRIAL NATRIURETIC FACTOR; DNA; MYOSIN HEAVY CHAIN; MYOSIN LIGHT CHAIN; T BOX TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR NKX; UNCLASSIFIED DRUG;

ALPHA CHAIN; AMINO ACID SUBSTITUTION; ANIMAL CELL; ARTICLE; ASSAY; BETA CHAIN; BINDING SITE; CONTROLLED STUDY; DATA BASE; DNA BINDING; DNA DETERMINATION; DNA FLANKING REGION; DNA SEQUENCE; GENE CONSTRUCT; GENE EXPRESSION; GENE MUTATION; GENETIC ANALYSIS; GENETIC TRANSCRIPTION; GENETIC TRANSFECTION; HOLT ORAM SYNDROME; IN VITRO STUDY; MOUSE; MULTIGENE FAMILY; NONHUMAN; PRIORITY JOURNAL; PROTEIN BINDING; RAT; REPORTER GENE;

EID: 0035445835     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/10.18.1983     Document Type: Article

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