Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome

Journal of Biological Chemistry

Volumn 279, Issue 21, 2004, Pages 22624-22634

  Nesbit, M Andrew ^a   Bowl, Michael R ^a   Harding, Brian ^a   Ali, Asif ^a   Ayala, Alejandro ^b   Crowe, Carol ^c   Dobbie, Angus ^d   Hampson, Geeta ^e   Holdaway, Ian ^f   Levine, Michael A ^g   McWilliams, Robert ^h   Rigden, Susan ⁱ   Sampson, Julian ^j   Williams, Andrew J ^k   Thakker, Rajesh V ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b NATIONAL INSTITUTES OF HEALTH   (United States)

^c METROHEALTH MEDICAL CENTER   (United States)

^d CHURCHILL HOSPITAL   (United Kingdom)

^e KING'S COLLEGE LONDON   (United Kingdom)

^f AUCKLAND CITY HOSPITAL   (New Zealand)

^g LERNER RESEARCH INSTITUTE   (United States)

^h MAYO CLINIC   (United States)

ⁱ GUY S HOSPITAL   (United Kingdom)

^j CARDIFF UNIVERSITY   (United Kingdom)

^k MORRISTON HOSPITAL   (United Kingdom)

more..

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; DNA; ELECTROPHORESIS; FUNCTIONS; MOLECULES; PROTEINS;

BINDING AFFINITY; BINDING SURFACES; DNA BINDING; MUTATIONS;

BIOCHEMISTRY;

AMINO ACID; ARGININE; ASPARAGINE; CYSTEINE; FOG PROTEIN; GLUTAMIC ACID; GLUTATHIONE TRANSFERASE; LYSINE; TRANSCRIPTION FACTOR GATA 3; UNCLASSIFIED DRUG; ZINC FINGER PROTEIN;

AMINO TERMINAL SEQUENCE; ANIMAL CELL; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BINDING AFFINITY; CARBOXY TERMINAL SEQUENCE; CLINICAL ARTICLE; CODON; DEVELOPMENTAL DISORDER; DISSOCIATION; FAMILY; FEMALE; FRAMESHIFT MUTATION; GENE DELETION; GENE MUTATION; HEARING IMPAIRMENT; HUMAN; HYPOPARATHYROIDISM; KIDNEY DYSPLASIA; MALE; MISSENSE MUTATION; NONHUMAN; NONSENSE MUTATION; PRIORITY JOURNAL; PROTEIN DNA BINDING; PROTEIN PROTEIN INTERACTION; TWO HYBRID SYSTEM;

ANIMALIA;

EID: 2542471328     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.M401797200     Document Type: Article

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