A novel mutation F826L in the human androgen receptor in partial androgen insensitivity syndrome; increased NH2-/COOH-terminal domain interaction and TIF2 co-activation.
about
Severe forms of partial androgen insensitivity syndrome due to p.L830F novel mutation in androgen receptor gene in a Brazilian family.The CAG repeat polymorphism in the androgen receptor gene modifies the risk for hypospadias in Caucasians.Coregulator control of androgen receptor action by a novel nuclear receptor-binding motif.Allosteric conversation in the androgen receptor ligand-binding domain surfaces.
P2860
A novel mutation F826L in the human androgen receptor in partial androgen insensitivity syndrome; increased NH2-/COOH-terminal domain interaction and TIF2 co-activation.
description
2008 nî lūn-bûn
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2008年の論文
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2008年学术文章
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2008年学术文章
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2008年学术文章
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2008年学术文章
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2008年学术文章
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2008年學術文章
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2008年學術文章
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2008年學術文章
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name
A novel mutation F826L in the ...... action and TIF2 co-activation.
@en
A novel mutation F826L in the ...... action and TIF2 co-activation.
@nl
type
label
A novel mutation F826L in the ...... action and TIF2 co-activation.
@en
A novel mutation F826L in the ...... action and TIF2 co-activation.
@nl
prefLabel
A novel mutation F826L in the ...... action and TIF2 co-activation.
@en
A novel mutation F826L in the ...... action and TIF2 co-activation.
@nl
P2093
P1476
A novel mutation F826L in the ...... raction and TIF2 co-activation
@en
P2093
Albert O Brinkmann
Cor A Berrevoets
Dennis Dooijes
Dennis J van de Wijngaart
Hao Yun Wong
Hendrikus Jan Dubbink
J Anton Grootegoed
Jan Trapman
Jos W Hoogerbrugge
Kar Lok Pang
P356
10.1016/J.MCE.2008.06.016
P577
2008-07-05T00:00:00Z