BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

296 related articles for article (PubMed ID: 11185742)

  • 21. Genetic analysis of a family with 46,XY "female" associated with infertility.
    Wang X; Wang XR; Liu MG; Wang Q; Liu JY
    Yi Chuan Xue Bao; 2006 Jan; 33(1):19-25. PubMed ID: 16450583
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Complete androgen insensitivity syndrome caused by a novel mutation in the ligand-binding domain of the androgen receptor: functional characterization.
    Rosa S; Biason-Lauber A; Mongan NP; Navratil F; Schoenle EJ
    J Clin Endocrinol Metab; 2002 Sep; 87(9):4378-82. PubMed ID: 12213902
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Clinical and genetic characterization of complete androgen insensitivity syndrome in a Chinese family.
    Li BK; Ding Q; Wan XD; Wang X
    Genet Mol Res; 2011 May; 10(2):1022-31. PubMed ID: 21710452
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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; 28(5):772-6. PubMed ID: 17522416
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [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]  

  • 27. In-vitro characterization of androgen receptor mutations associated with complete androgen insensitivity syndrome reveals distinct functional deficits.
    Werner R; Zhan J; Gesing J; Struve D; Hiort O
    Sex Dev; 2008; 2(2):73-83. PubMed ID: 18577874
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Analysis of exon 1 mutations in the androgen receptor gene.
    Gottlieb B; Vasiliou DM; Lumbroso R; Beitel LK; Pinsky L; Trifiro MA
    Hum Mutat; 1999; 14(6):527-39. PubMed ID: 10571951
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. A novel E153X point mutation in the androgen receptor gene in a patient with complete androgen insensitivity syndrome.
    Copelli SB; Lumbroso S; Audran F; Pellizzari EH; Heinrich JJ; Cigorraga SB; Sultan C; Chemes HE
    Asian J Androl; 1999 Jun; 1(1-2):73-7. PubMed ID: 11225909
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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(6):921-31. PubMed ID: 16449235
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. [Deletion of thymine at position 2298 in exon 5 of the androgenic receptor gene causing complete androgen insensitivity syndrome].
    Soriano Guillén L; Muñoz Calvo MT; Martinez Pérez J; Pozo Román J; Martín Sobrino MA; González Medeiro I; Argente Oliver J
    An Esp Pediatr; 2002 Apr; 56(4):347-52. PubMed ID: 11927080
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Complete androgen insensitivity syndrome is frequently due to premature stop codons in exon 1 of the androgen receptor gene: an international collaborative report of 13 new mutations.
    Philibert P; Audran F; Pienkowski C; Morange I; Kohler B; Flori E; Heinrich C; Dacou-Voutetakis C; Joseph MG; Guedj AM; Journel H; Hecart-Bruna AC; Khotchali I; Ten S; Bouchard P; Paris F; Sultan C
    Fertil Steril; 2010 Jul; 94(2):472-6. PubMed ID: 19463997
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Identification of a novel mutation in exon 1 of androgen receptor gene in an azoospermic patient with mild androgen insensitivity syndrome: case report and literature review.
    Goglia U; Vinanzi C; Zuccarello D; Malpassi D; Ameri P; Casu M; Minuto F; Foresta C; Ferone D
    Fertil Steril; 2011 Nov; 96(5):1165-9. PubMed ID: 21962961
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Gene symbol: AR. Disease: androgen insensitivity syndrome.
    Turek-Plewa J; Trzeciak WH
    Hum Genet; 2006 Apr; 119(3):361. PubMed ID: 17230651
    [No Abstract]   [Full Text] [Related]  

  • 39. Novel androgen receptor gene mutations in Australian patients with complete androgen insensitivity syndrome.
    MacLean HE; Ball EM; Rekaris G; Warne GL; Zajac JD
    Hum Mutat; 2004 Mar; 23(3):287. PubMed ID: 14974091
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Phenotypic features, androgen receptor binding, and mutational analysis in 278 clinical cases reported as androgen insensitivity syndrome.
    Ahmed SF; Cheng A; Dovey L; Hawkins JR; Martin H; Rowland J; Shimura N; Tait AD; Hughes IA
    J Clin Endocrinol Metab; 2000 Feb; 85(2):658-65. PubMed ID: 10690872
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.