Androgen receptor mutations associated with androgen insensitivity syndrome: A high content analysis approach leading to personalized medicine

Advances in Experimental Medicine and Biology

Volumn 707, Issue , 2011, Pages 63-65

  Szafran, Adam T ^b   Sun, Huiying ^b   Hartig, Sean ^b   Shen, Yuqing ^b   Mediwala, Sanjay N ^b   Bell, Jennifer ^b   McPhaul, Michael J ^b   Mancini, Michael A ^b   Marcelli, Marco ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b Michael E DeBakey VA Medical Center ^*

Author keywords

[No Author keywords available]

Indexed keywords

ANDROGEN RECEPTOR; MIBOLERONE; MUTANT PROTEIN;

AMINO TERMINAL SEQUENCE; ANALYTIC METHOD; ANDROGEN INSENSITIVITY SYNDROME; ANDROGEN RECEPTOR GENE; ARTICLE; BINDING SITE; CASE REPORT; COMPLETE ANDROGEN INSENSITIVITY SYNDROME; CONTROLLED STUDY; DISSOCIATION CONSTANT; GENE; GENE FUNCTION; GENE MUTATION; HIGH CONTENT ANALYSIS; HUMAN; HUMAN CELL; LIGAND BINDING; PARTIAL ANDROGEN INSENSITIVITY SYNDROME; PRIORITY JOURNAL; PROTEIN LOCALIZATION; RECEPTOR BINDING; SKIN FIBROBLAST; TWO HYBRID SYSTEM;

ANDROGEN-INSENSITIVITY SYNDROME; HELA CELLS; HUMANS; INDIVIDUALIZED MEDICINE; MALE; MUTATION;

EID: 79960705846     PISSN: 00652598     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-1-4419-8002-1_15     Document Type: Article

References (1)

1. Szafran, A.T., Szwarc, M., Marcelli, M., and Mancini, M.A. 2008. Androgen receptor functional analyses by high throughput imaging: Determination of ligand, cell cycle, and mutation-specific effects. PLoS One 3:e3605.