The TPIT gene mutation M86R associated with isolated adrenocorticotropin deficiency interferes with protein: Protein interactions

Journal of Clinical Endocrinology and Metabolism

Volumn 92, Issue 10, 2007, Pages 3991-3999

  Vallette Kasic, Sophie ^a   Couture, Catherine ^a   Balsalobre, Aurelio ^a   Gauthier, Yves ^a   Metherell, Louise ^b   Dattani, Mehul ^c   Drouin, Jacques ^a  

^a CLIN RESEARCH INSTITUTE OF MONTREAL   (Canada)

^b QUEEN MARY UNIVERSITY OF LONDON   (United Kingdom)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CORTICOTROPIN; HOMODIMER; MONOMER; NUCLEAR RECEPTOR COACTIVATOR 2; PROOPIOMELANOCORTIN; T BOX TRANSCRIPTION FACTOR;

ARTICLE; BINDING AFFINITY; CONTROLLED STUDY; CORTICOTROPIN DEFICIENCY; DNA BINDING; ENZYME ACTIVATION; GENE MUTATION; GENETIC TRANSCRIPTION; HUMAN; HUMAN CELL; M86R GENE; PRIORITY JOURNAL; PROTEIN INTERACTION;

MURINAE;

EID: 34548135041     PISSN: 0021972X     EISSN: 0021972X     Source Type: Journal    
DOI: 10.1210/jc.2007-0284     Document Type: Article

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