A novel TRβ mutation (R383H) in resistance to thyroid hormone syndrome predominantly impairs corepressor release and negative transcriptional regulation

Molecular Endocrinology

Volumn 12, Issue 5, 1998, Pages 609-621

  Clifton Bligh, R J ^a   De Zegher, F ^a   Wagner, R L ^a   Collingwood, T N ^a   Francois, I ^a   Van Helvoirt, M ^a   Fletterick, R J ^a   Chatterjee, V K K ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

LIOTHYRONINE; PROTIRELIN; RETINOID X RECEPTOR; THYROID HORMONE; THYROID HORMONE RECEPTOR; THYROTROPIN;

ARTICLE; BINDING AFFINITY; CASE REPORT; CHILD; CLINICAL FEATURE; FEMALE; GENE MUTATION; HORMONE RECEPTOR INTERACTION; HORMONE RESPONSIVE ELEMENT; HUMAN; PATHOGENESIS; PRIORITY JOURNAL; PROMOTER REGION; THYROID HORMONE BLOOD LEVEL; THYROID HORMONE RESISTANCE; TRANSACTIVATION; TRANSCRIPTION REGULATION;

EID: 0032230336     PISSN: 08888809     EISSN: None     Source Type: Journal    
DOI: 10.1210/mend.12.5.0113     Document Type: Article

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