Androgen Receptor Exon 1 Mutation Causes Androgen Insensitivity by Creating Phosphorylation Site and Inhibiting Melanoma Antigen-A11 Activation of NH(2)- and Carboxyl-terminal Interaction-dependent Transactivation

Naturally occurring germ line mutations in the X-linked human androgen receptor (AR) gene cause incomplete masculinization of the external genitalia by disrupting AR function in males with androgen insensitivity syndrome. Almost all AR missense mutations that cause androgen insensitivity syndrome ar...

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Bibliografiska uppgifter
Huvudupphovsmän: Lagarde, William H., Blackwelder, Amanda J., Minges, John T., Hnat, Andrew T., French, Frank S., Wilson, Elizabeth M.
Materialtyp: Artigo
Språk:Inglês
Publicerad: American Society for Biochemistry and Molecular Biology 2012
Ämnen:
Gene Regulation
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3322816/
https://ncbi.nlm.nih.gov/pubmed/22334658
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M111.336081
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