Partial androgen insensitivity with phenotypic variation caused by androgen receptor mutations that disrupt activation function 2 and the NH2- and carboxyl-terminal interaction-Reference-Cited by-同舟云学术

Partial androgen insensitivity with phenotypic variation caused by androgen receptor mutations that disrupt activation function 2 and the NH2- and carboxyl-terminal interaction

Published:2004-10 Issue:10-11 Volume:125 Page:683-695
ISSN:0047-6374
Container-title:Mechanisms of Ageing and Development
language:en
Short-container-title:Mechanisms of Ageing and Development

Author:

Quigley Charmian A.,Tan Jiann-an,He Bin,Zhou Zhong-xun,Mebarki Farida,Morel Yves,Forest Maguelone G.,Chatelain Pierre,Ritzén E. Martin,French Frank S.,Wilson Elizabeth M.

Publisher

Elsevier BV

Subject

Developmental Biology,Aging

Reference93 articles.

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2. The androgen receptor amino-terminal domain plays a key role in p160 coactivator-stimulated gene transcription;Alen;Mol. Cell. Biol.,1999

3. Phenotypic variation and detection of carrier status in the partial androgen insensitivity syndrome;Batch;Arch. Dis. Child.,1993

4. Functional interactions of the AF-2 activation domain core region of the human androgen receptor with the amino-terminal domain and with the transcriptional coactivator TIF2;Berrevoets;Mol. Endocrinol.,1998

5. Germ-line and somatic mosaicism in the androgen insensitivity syndrome: implications for genetic counselling;Boehmer;Am. J. Hum. Genet.,1997

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