These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 12084976)

  • 21. Complete androgen insensitivity without Wolffian duct development: the AR-A form of the androgen receptor is not sufficient for male genital development.
    Barbaro M; Oscarson M; Almskog I; Hamberg H; Wedell A
    Clin Endocrinol (Oxf); 2007 Jun; 66(6):822-6. PubMed ID: 17408421
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Characterization of a novel receptor mutation A-->T at exon 4 in complete androgen insensitivity syndrome and a carrier sibling via bidirectional polymorphism sequence analysis.
    Sills ES; Sholes TE; Perloe M; Kaplan CR; Davis JG; Tucker MJ
    Int J Mol Med; 2002 Jan; 9(1):45-8. PubMed ID: 11744994
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A novel mutation in the CAG triplet region of exon 1 of androgen receptor gene causes complete androgen insensitivity syndrome in a large kindred.
    Zhu YS; Cai LQ; Cordero JJ; Canovatchel WJ; Katz MD; Imperato-McGinley J
    J Clin Endocrinol Metab; 1999 May; 84(5):1590-4. PubMed ID: 10323385
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A novel mutation (c.T3816 > C) in the androgen receptor gene in a 46,XY female patient with androgen insensitivity syndrome.
    Helszer Z; Dmochowska A; Borkowska E; Moczulska H; Słowikowska-Hilczer J; Pietrusiński M; Jędrzejczyk S; Kałużewski B
    Endokrynol Pol; 2013; 64(5):398-402. PubMed ID: 24186597
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Androgen resistance.
    Hughes IA; Deeb A
    Best Pract Res Clin Endocrinol Metab; 2006 Dec; 20(4):577-98. PubMed ID: 17161333
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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; 125(10-11):683-95. PubMed ID: 15541764
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A novel androgen receptor mutation resulting in complete androgen insensitivity syndrome and bilateral Leydig cell hyperplasia.
    Singh R; Shastry PK; Rasalkar AA; Singh L; Thangaraj K
    J Androl; 2006; 27(4):510-6. PubMed ID: 16582414
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genotype versus phenotype in families with androgen insensitivity syndrome.
    Boehmer AL; Brinkmann O; Brüggenwirth H; van Assendelft C; Otten BJ; Verleun-Mooijman MC; Niermeijer MF; Brunner HG; Rouwé CW; Waelkens JJ; Oostdijk W; Kleijer WJ; van der Kwast TH; de Vroede MA; Drop SL
    J Clin Endocrinol Metab; 2001 Sep; 86(9):4151-60. PubMed ID: 11549642
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Identification of a novel frameshift mutation of human androgen receptor gene in a patient featuring complete androgen insensitivity syndrome].
    Xie JH; Qu JH; Xiao QZ; Zhou YQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):99-101. PubMed ID: 23450491
    [TBL] [Abstract][Full Text] [Related]  

  • 30. GTG mutation in the start codon of the androgen receptor gene in a family of horses with 64,XY disorder of sex development.
    Révay T; Villagómez DA; Brewer D; Chenier T; King WA
    Sex Dev; 2012; 6(1-3):108-16. PubMed ID: 22095250
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [A novel mutation Glu441stop (GAA to TAA) of androgen receptor gene resulting in complete androgen insensitivity syndrome].
    LUO FW; WU WQ; GENG Q; LI F; CHEN WB; GAN WX; XIE JS
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Apr; 28(2):176-9. PubMed ID: 21462130
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A novel point mutation (R840S) in the androgen receptor in a Brazilian family with partial androgen insensitivity syndrome.
    Melo KF; Latronico AC; Costa EM; Billerbeck AE; Mendonca BB; Arnhold IJ
    Hum Mutat; 1999 Oct; 14(4):353. PubMed ID: 10502786
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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; 22(6):465-75. PubMed ID: 14635106
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Correlation between genotype, phenotype and sex of rearing in 111 patients with partial androgen insensitivity syndrome.
    Deeb A; Mason C; Lee YS; Hughes IA
    Clin Endocrinol (Oxf); 2005 Jul; 63(1):56-62. PubMed ID: 15963062
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Pathogenesis of androgen insensitivity syndrome].
    Okabe T; Nawata H
    Nihon Rinsho; 1998 Jul; 56(7):1881-6. PubMed ID: 9702070
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Androgen insensitivity].
    Stárka L; Hampl R
    Cas Lek Cesk; 1994 Jun; 133(13):387-90. PubMed ID: 8062328
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [An acceptor-splice-site mutation responsible for complete androgen insensitivity syndrome].
    Zhang W; Li X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Feb; 18(1):14-6. PubMed ID: 11172634
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Ala 586 Asp mutation in androgen receptor disrupts transactivation function without affecting androgen binding.
    Rajender S; Gupta NJ; Chakrabarty B; Singh L; Thangaraj K
    Fertil Steril; 2009 Mar; 91(3):933.e23-8. PubMed ID: 19062009
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Partial androgen insensitivity syndrome with R840H mutation in androgen receptor: report of one case.
    Yen JL; Chang KH; Sheu JC; Lee YJ; Tsai LP
    Acta Paediatr Taiwan; 2005; 46(2):101-5. PubMed ID: 16302589
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genetic counselling in complete androgen insensitivity syndrome: trinucleotide repeat polymorphisms, single-strand conformation polymorphism and direct detection of two novel mutations in the androgen receptor gene.
    Davies HR; Hughes IA; Patterson MN
    Clin Endocrinol (Oxf); 1995 Jul; 43(1):69-77. PubMed ID: 7641413
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.