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Journal Abstract Search

148 related items for PubMed ID: 11818512

  • 1. Androgen receptor mutations causing human androgen insensitivity syndromes show a key role of residue M807 in Helix 8-Helix 10 interactions and in receptor ligand-binding domain stability.
    Ong YC, Kolatkar PR, Yong EL.
    Mol Hum Reprod; 2002 Feb; 8(2):101-8. PubMed ID: 11818512
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  • 4. 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 Feb; 6(2):152-62. PubMed ID: 7581399
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  • 5. 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 Feb; 28(5):772-6. PubMed ID: 17522416
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  • 6. Partial androgen insensitivity with phenotypic variation caused by androgen receptor mutations that disrupt activation function 2 and the NH(2)- and carboxyl-terminal interaction.
    Quigley CA, Tan JA, He B, Zhou ZX, Mebarki F, Morel Y, Forest MG, Chatelain P, Ritzén EM, French FS, Wilson EM.
    Mech Ageing Dev; 2004 Feb; 125(10-11):683-95. PubMed ID: 15541764
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  • 8. A new mutation of the androgen receptor, P817A, causing partial androgen insensitivity syndrome: in vitro and structural analysis.
    Lumbroso S, Wagschal A, Bourguet W, Georget V, Mazen I, Servant N, Audran F, Sultan C, Auzou G.
    J Mol Endocrinol; 2004 Jun; 32(3):679-87. PubMed ID: 15171708
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  • 9. Disrupted amino- and carboxyl-terminal interactions of the androgen receptor are linked to androgen insensitivity.
    Thompson J, Saatcioglu F, Jänne OA, Palvimo JJ.
    Mol Endocrinol; 2001 Jun; 15(6):923-35. PubMed ID: 11376111
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  • 12. A G577R mutation in the human AR P box results in selective decreases in DNA binding and in partial androgen insensitivity syndrome.
    Nguyen D, Steinberg SV, Rouault E, Chagnon S, Gottlieb B, Pinsky L, Trifiro M, Mader S.
    Mol Endocrinol; 2001 Oct; 15(10):1790-802. PubMed ID: 11579211
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  • 13. Five novel androgen receptor gene mutations associated with complete androgen insensitivity syndrome.
    Jääskeläinen J, Mongan NP, Harland S, Hughes IA.
    Hum Mutat; 2006 Mar; 27(3):291. PubMed ID: 16470553
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  • 14. Impaired nuclear translocation, nuclear matrix targeting, and intranuclear mobility of mutant androgen receptors carrying amino acid substitutions in the deoxyribonucleic acid-binding domain derived from androgen insensitivity syndrome patients.
    Kawate H, Wu Y, Ohnaka K, Tao RH, Nakamura K, Okabe T, Yanase T, Nawata H, Takayanagi R.
    J Clin Endocrinol Metab; 2005 Nov; 90(11):6162-9. PubMed ID: 16118342
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  • 15. A novel mutation F826L in the human androgen receptor in partial androgen insensitivity syndrome; increased NH2-/COOH-terminal domain interaction and TIF2 co-activation.
    Wong HY, Hoogerbrugge JW, Pang KL, van Leeuwen M, van Royen ME, Molier M, Berrevoets CA, Dooijes D, Dubbink HJ, van de Wijngaart DJ, Wolffenbuttel KP, Trapman J, Kleijer WJ, Drop SL, Grootegoed JA, Brinkmann AO.
    Mol Cell Endocrinol; 2008 Sep 24; 292(1-2):69-78. PubMed ID: 18656523
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  • 18. Human androgen receptor mutation disrupts ternary interactions between ligand, receptor domains, and the coactivator TIF2 (transcription intermediary factor 2).
    Lim J, Ghadessy FJ, Abdullah AA, Pinsky L, Trifiro M, Yong EL.
    Mol Endocrinol; 2000 Aug 24; 14(8):1187-97. PubMed ID: 10935543
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  • 19. L712V mutation in the androgen receptor gene causes complete androgen insensitivity syndrome due to severe loss of androgen function.
    Rajender S, Gupta NJ, Chakrabarty B, Singh L, Thangaraj K.
    Steroids; 2013 Dec 11; 78(12-13):1288-92. PubMed ID: 24055831
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  • 20. Androgen receptor gene and male infertility.
    Yong EL, Loy CJ, Sim KS.
    Hum Reprod Update; 2003 Dec 11; 9(1):1-7. PubMed ID: 12638777
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