Androgen receptor mutations causing human androgen insensitivity syndromes show a key role of residue M807 in helix 8-helix 10 interactions and in receptor ligand-binding domain stability

Molecular Human Reproduction

Volumn 8, Issue 2, 2002, Pages 101-108

  Ong, Y C ^a   Kolatkar, P R ^a   Yong, E L ^a  

^a NATIONAL UNIVERSITY OF SINGAPORE   (Singapore)

Author keywords

Androgen receptor; Helical stability; Mutations

Indexed keywords

ANDROGEN RECEPTOR; ARGININE; CELL NUCLEUS RECEPTOR; ESTROGEN RECEPTOR ALPHA; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR GAMMA; STEROID RECEPTOR; THREONINE; VALINE;

ALPHA HELIX; AMINO ACID SUBSTITUTION; ANDROGEN INSENSITIVITY SYNDROME; ANIMAL CELL; ARTICLE; CASE REPORT; CONTROLLED STUDY; GENETIC CONSERVATION; GENITAL MALFORMATION; HUMAN; HUMAN CELL; INFANT; KARYOTYPE 46,XY; LIGAND BINDING; MALE; MISSENSE MUTATION; NONHUMAN; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN FAMILY; PROTEIN INTERACTION; PROTEIN STABILITY; PROTEIN STRUCTURE; TRANSACTIVATION;

ANIMALIA;

EID: 0036166569     PISSN: 13609947     EISSN: None     Source Type: Journal    
DOI: 10.1093/molehr/8.2.101     Document Type: Article

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