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From The Department of Otolaryngology, University of Iowa, Iowa City, Iowa.
| Correspondence to: Dr Xinchang Zhou, The Department of Otolaryngology, University of Iowa, 5270 CBRB, Iowa City, IA 52242 (e-mail: xinchang-zhou{at}uiowa.edu). |
The androgen receptor (AR), a member of the nuclear receptor superfamily,
is a ligand-dependent transcription factor involved in regulating expression
of an array of androgen-responsive genes. AR-mediated androgen actions play
the important roles in male and female reproductive development and function.
AR mutations can cause a diverse range of diseases, such as testicular
feminization mutation (Tfm) syndrome, prostate cancer, and Kennedy's disease.
However, because of a lack of genetic models, the molecular mechanisms
involved in the physiological and pathological effects of androgen–AR
function in male and female reproductive health remains largely unknown. To
get a better insight into the molecular working mechanisms of the AR, a global
and several cell-specific conditional knockout mouse models have been
developed. These models are reviewed here, and the phenotypes of the different
cell-specific androgen receptor knockout (ARKO) mice are compared with those
of the global ARKO mice.
Key words: Nuclear receptor, conditional knockout, phenotype
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