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Journal Abstract Search

169 related items for 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
    [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
    [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
    [Abstract] [Full Text] [Related]

  • 24. [Clinical consequences of androgen receptor malfunction].
    Klocker H, Eder IE, Culig Z, Bartsch G.
    Verh Dtsch Ges Pathol; 2004 Feb; 88():122-9. PubMed ID: 16892542
    [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 Feb; 27(4):510-6. PubMed ID: 16582414
    [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 24; 292(1-2):69-78. PubMed ID: 18656523
    [Abstract] [Full Text] [Related]

  • 27. [Androgen receptor and insensitivity to androgens].
    Mowszowicz I, Kuttenn F.
    Rev Prat; 1994 May 15; 44(10):1304-9. PubMed ID: 7939189
    [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; 15(6):921-31. PubMed ID: 16449235
    [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 15; 7(5):1273-81. PubMed ID: 11350894
    [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 15; 20(3):217-28. PubMed ID: 12428202
    [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 15; 14(4):353. PubMed ID: 10502786
    [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 Oct 15; 8(1):7-12. PubMed ID: 9101272
    [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 Oct 15; 3(5):237-44. PubMed ID: 19851057
    [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 15; 65(5):606-10. PubMed ID: 17054461
    [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 Nov 15; 28(2):125-9. PubMed ID: 3876063
    [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 Nov 15; 62(5):259-64. PubMed ID: 15528927
    [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 15; 18(1):14-6. PubMed ID: 11172634
    [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 15; 9(1):45-8. PubMed ID: 11744994
    [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 15; 47(1-6):127-35. PubMed ID: 8274427
    [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 15; 1(1-2):73-7. PubMed ID: 11225909
    [Abstract] [Full Text] [Related]

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