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Journal Abstract Search

504 related items for PubMed ID: 16449235

  • 1. Impaired helix 12 dynamics due to proline 892 substitutions in the androgen receptor are associated with complete androgen insensitivity.
    Elhaji YA, Stoica I, Dennis S, Purisima EO, Lumbroso R, Beitel LK, Trifiro MA.
    Hum Mol Genet; 2006 Mar 15; 15(6):921-31. PubMed ID: 16449235
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  • 3. Bridging structural biology and genetics by computational methods: an investigation into how the R774C mutation in the AR gene can result in complete androgen insensitivity syndrome.
    Wu JH, Gottlieb B, Batist G, Sulea T, Purisima EO, Beitel LK, Trifiro M.
    Hum Mutat; 2003 Dec 15; 22(6):465-75. PubMed ID: 14635106
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  • 8. L859F mutation in androgen receptor gene results in complete loss of androgen binding to the receptor.
    Rajender S, Singh L, Thangaraj K.
    J Androl; 2007 Dec 15; 28(5):772-6. PubMed ID: 17522416
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  • 10. Human androgen insensitivity due to point mutations encoding amino acid substitutions in the androgen receptor steroid-binding domain.
    Murono K, Mendonca BB, Arnhold IJ, Rigon AC, Migeon CJ, Brown TR.
    Hum Mutat; 1995 Dec 15; 6(2):152-62. PubMed ID: 7581399
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  • 20. [Mutation analysis of the androgen receptor gene in a complete androgen insensitivity syndrome family].
    Wu W, Luo F, Geng Q, Hao Y, Chen W, Cai J, Xie J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec 15; 26(6):606-9. PubMed ID: 19953479
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