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 *

168 related articles for article (PubMed ID: 9302173)

  • 21. 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]  

  • 22. 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]  

  • 23. Male pseudohermaphroditism with partial androgen insensitivity.
    Keenan BS; Kirkland JL; Kirkland RT; Clayton GW
    Pediatrics; 1977 Feb; 59(2):224-31. PubMed ID: 834506
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Clinical consequences of androgen receptor malfunction].
    Klocker H; Eder IE; Culig Z; Bartsch G
    Verh Dtsch Ges Pathol; 2004; 88():122-9. PubMed ID: 16892542
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. 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; 292(1-2):69-78. PubMed ID: 18656523
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Androgen receptor and insensitivity to androgens].
    Mowszowicz I; Kuttenn F
    Rev Prat; 1994 May; 44(10):1304-9. PubMed ID: 7939189
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Collocation of androgen receptor gene mutations in prostate cancer.
    Buchanan G; Greenberg NM; Scher HI; Harris JM; Marshall VR; Tilley WD
    Clin Cancer Res; 2001 May; 7(5):1273-81. PubMed ID: 11350894
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Disorders of androgen action.
    Sultan C; Lumbroso S; Paris F; Jeandel C; Terouanne B; Belon C; Audran F; Poujol N; Georget V; Gobinet J; Jalaguier S; Auzou G; Nicolas JC
    Semin Reprod Med; 2002 Aug; 20(3):217-28. PubMed ID: 12428202
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Complete androgen insensitivity syndrome: clinical and anatomopathological findings in 23 patients.
    Alvarez-Nava F; Gonzalez S; Soto M; Martinez C; Prieto M
    Genet Couns; 1997; 8(1):7-12. PubMed ID: 9101272
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Functional analysis of novel androgen receptor mutations in a unique cohort of Indonesian patients with a disorder of sex development.
    Elfferich P; Juniarto AZ; Dubbink HJ; van Royen ME; Molier M; Hoogerbrugge J; Houtsmuller AB; Trapman J; Santosa A; de Jong FH; Drop SL; Faradz SM; Bruggenwirth H; Brinkmann AO
    Sex Dev; 2009; 3(5):237-44. PubMed ID: 19851057
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Male infertility and androgen receptor gene mutations: clinical features and identification of seven novel mutations.
    Ferlin A; Vinanzi C; Garolla A; Selice R; Zuccarello D; Cazzadore C; Foresta C
    Clin Endocrinol (Oxf); 2006 Nov; 65(5):606-10. PubMed ID: 17054461
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A case of male pseudohermaphroditism with normal androgen receptor binding and 47,XYY karyotype.
    Bosch-Banyeras JM; Audi L; Sarret E; Bau A; Bosch-Marcet J; Bernet M; Iriondo L; Cuatrecasas JM
    Ann Genet; 1985; 28(2):125-9. PubMed ID: 3876063
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Clinical, biochemical and morphologic diagnostic markers in an infant male pseudohermaphrodite patient with compound heterozygous mutations (G115D/R246W) in SRD5A2 gene.
    Fernández-Cancio M; Rodó J; Andaluz P; Martínez de Osaba MJ; Rodríguez-Hierro F; Esteban C; Carrascosa A; Audí L
    Horm Res; 2004; 62(5):259-64. PubMed ID: 15528927
    [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. 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]  

  • 39. Characterization of two point mutations in the androgen receptor gene of patients with perineoscrotal hypospadia.
    Kaspar F; Cato AC; Denninger A; Eberle J; Radmayr C; Glatzl J; Bartsch G; Klocker H
    J Steroid Biochem Mol Biol; 1993 Dec; 47(1-6):127-35. PubMed ID: 8274427
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 9.