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Journal Abstract Search

257 related items for PubMed ID: 27994190

  • 21.
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  • 22. Investigation of androgen receptor gene mutations in a series of 21 patients with 46,XY disorders of sex development.
    Topcu V, Ilgin-Ruhi H, Siklar Z, Karabulut HG, Berberoglu M, Hacihamdioglu B, Savas-Erdeve S, Aycan Z, Peltek-Kendirci HN, Ocal G, Tukun FA.
    J Pediatr Endocrinol Metab; 2015 Nov 01; 28(11-12):1257-63. PubMed ID: 26197461
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  • 23. Molecular biology of androgen insensitivity.
    Jääskeläinen J.
    Mol Cell Endocrinol; 2012 Apr 16; 352(1-2):4-12. PubMed ID: 21871529
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  • 25. A recurrent synonymous mutation in the human androgen receptor gene causing complete androgen insensitivity syndrome.
    Batista RL, Rodrigues ADS, Nishi MY, Gomes NL, Faria JAD, Moraes DR, Carvalho LR, Costa EMF, Domenice S, Mendonca BB.
    J Steroid Biochem Mol Biol; 2017 Nov 16; 174():14-16. PubMed ID: 28743543
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  • 29. A novel mutation of the androgen receptor gene in familial complete androgen insensitivity syndrome.
    Li Y, Qu S, Li P.
    Eur Rev Med Pharmacol Sci; 2015 Nov 16; 19(21):4146-52. PubMed ID: 26592841
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  • 31. Single base mutations in the human androgen receptor gene causing complete androgen insensitivity: rapid detection by a modified denaturing gradient gel electrophoresis technique.
    De Bellis A, Quigley CA, Cariello NF, el-Awady MK, Sar M, Lane MV, Wilson EM, French FS.
    Mol Endocrinol; 1992 Nov 16; 6(11):1909-20. PubMed ID: 1480178
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  • 32. 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 16; 87(9):4378-82. PubMed ID: 12213902
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  • 33. 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 16; 84(5):1590-4. PubMed ID: 10323385
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  • 34. Prenatal diagnosis of androgen insensitivity syndrome.
    Bianca S, Cataliotti A, Bartoloni G, Torrente I, Barrano B, Boemi G, Lo Presti M, Indaco L, Barone C, Ettore G.
    Fetal Diagn Ther; 2009 May 16; 26(3):167-9. PubMed ID: 19844078
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  • 35. Mutations of androgen receptor gene in androgen insensitivity syndromes.
    Sultan C, Lumbroso S, Poujol N, Belon C, Boudon C, Lobaccaro JM.
    J Steroid Biochem Mol Biol; 1993 Nov 16; 46(5):519-30. PubMed ID: 8240973
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  • 36. Eight novel mutations of the androgen receptor gene in patients with androgen insensitivity syndrome.
    Chávez B, Méndez JP, Ulloa-Aguirre A, Larrea F, Vilchis F.
    J Hum Genet; 2001 Nov 16; 46(10):560-5. PubMed ID: 11587068
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  • 37. Mutational analysis of the androgen receptor (NR3C4) gene in patients with 46,XY DSD.
    Ramos L, Chávez B, Mares L, Valdés E, Vilchis F.
    Gene; 2018 Jan 30; 641():86-93. PubMed ID: 29051026
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