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236 related items for PubMed ID: 2186053
1. Analysis of gonadotropin-releasing hormone gene structure in families with familial central precocious puberty and idiopathic hypogonadotropic hypogonadism. Nakayama Y, Wondisford FE, Lash RW, Bale AE, Weintraub BD, Cutler GB, Radovick S. J Clin Endocrinol Metab; 1990 May; 70(5):1233-8. PubMed ID: 2186053 [Abstract] [Full Text] [Related]
2. Normal structure of the gonadotropin-releasing hormone (GnRH) gene in patients with GnRH deficiency and idiopathic hypogonadotropic hypogonadism. Weiss J, Crowley WF, Jameson JL. J Clin Endocrinol Metab; 1989 Aug; 69(2):299-303. PubMed ID: 2546961 [Abstract] [Full Text] [Related]
4. Molecular analysis of the neuropeptide Y1 receptor gene in human idiopathic gonadotropin-dependent precocious puberty and isolated hypogonadotropic hypogonadism. Freitas KC, Ryan G, Brito VN, Tao YX, Costa EM, Mendonca BB, Segaloff D, Latronico AC. Fertil Steril; 2007 Mar; 87(3):627-34. PubMed ID: 17140570 [Abstract] [Full Text] [Related]
5. Mutation analysis of the gonadotropin-releasing hormone receptor gene in idiopathic hypogonadotropic hypogonadism. Layman LC, Peak DB, Xie J, Sohn SH, Reindollar RH, Gray MR. Fertil Steril; 1997 Dec; 68(6):1079-85. PubMed ID: 9418701 [Abstract] [Full Text] [Related]
6. Normal sequence of the gonadotropin-releasing hormone gene in patients with idiopathic hypogonadotropic hypogonadism. Weiss J, Adams E, Whitcomb RW, Crowley WF, Jameson JL. Biol Reprod; 1991 Nov; 45(5):743-7. PubMed ID: 1756212 [Abstract] [Full Text] [Related]
7. The GPR54 gene as a regulator of puberty. Seminara SB, Messager S, Chatzidaki EE, Thresher RR, Acierno JS, Shagoury JK, Bo-Abbas Y, Kuohung W, Schwinof KM, Hendrick AG, Zahn D, Dixon J, Kaiser UB, Slaugenhaupt SA, Gusella JF, O'Rahilly S, Carlton MB, Crowley WF, Aparicio SA, Colledge WH. N Engl J Med; 2003 Oct 23; 349(17):1614-27. PubMed ID: 14573733 [Abstract] [Full Text] [Related]
8. [Kisspeptin and leptin in the regulation of fertility]. Pankov YA. Mol Biol (Mosk); 2015 Oct 23; 49(5):707-15. PubMed ID: 26510589 [Abstract] [Full Text] [Related]
9. Autosomal recessive idiopathic hypogonadotropic hypogonadism: genetic analysis excludes mutations in the gonadotropin-releasing hormone (GnRH) and GnRH receptor genes. Bo-Abbas Y, Acierno JS, Shagoury JK, Crowley WF, Seminara SB. J Clin Endocrinol Metab; 2003 Jun 23; 88(6):2730-7. PubMed ID: 12788881 [Abstract] [Full Text] [Related]
10. Familial gonadotropin-releasing hormone resistance and hypogonadotropic hypogonadism in a family with multiple affected individuals. Layman LC, McDonough PG, Cohen DP, Maddox M, Tho SP, Reindollar RH. Fertil Steril; 2001 Jun 23; 75(6):1148-55. PubMed ID: 11384641 [Abstract] [Full Text] [Related]
11. The gonadotropin-releasing hormone (GnRH)-1 gene, the GnRH receptor gene, and their promoters in patients with idiopathic hypogonadotropic hypogonadism with or without resistance to GnRH action. Vagenakis GA, Sgourou A, Papachatzopoulou A, Kourounis G, Papavassiliou AG, Georgopoulos NA. Fertil Steril; 2005 Dec 23; 84(6):1762-5. PubMed ID: 16359986 [Abstract] [Full Text] [Related]
12. The same molecular defects of the gonadotropin-releasing hormone receptor determine a variable degree of hypogonadism in affected kindred. de Roux N, Young J, Brailly-Tabard S, Misrahi M, Milgrom E, Schaison G. J Clin Endocrinol Metab; 1999 Feb 23; 84(2):567-72. PubMed ID: 10022417 [Abstract] [Full Text] [Related]
13. KISS1 gene analysis in Korean girls with central precocious puberty: a polymorphism, p.P110T, suggested to exert a protective effect. Ko JM, Lee HS, Hwang JS. Endocr J; 2010 Feb 23; 57(8):701-9. PubMed ID: 20631455 [Abstract] [Full Text] [Related]
14. A novel DAX-1 mutation presented with precocious puberty and hypogonadotropic hypogonadism in different members of a large pedigree. Durmaz E, Turkkahraman D, Berdeli A, Atan M, Karaguzel G, Akcurin S, Bircan I. J Pediatr Endocrinol Metab; 2013 Feb 23; 26(5-6):551-5. PubMed ID: 23585174 [Abstract] [Full Text] [Related]
15. A sporadic case of male-limited precocious puberty has the same constitutively activating point mutation in luteinizing hormone/choriogonadotropin receptor gene as familial cases. Yano K, Hidaka A, Saji M, Polymeropoulos MH, Okuno A, Kohn LD, Cutler GB. J Clin Endocrinol Metab; 1994 Dec 23; 79(6):1818-23. PubMed ID: 7527413 [Abstract] [Full Text] [Related]
16. New mutations of DAX-1 genes in two Japanese patients with X-linked congenital adrenal hypoplasia and hypogonadotropic hypogonadism. Yanase T, Takayanagi R, Oba K, Nishi Y, Ohe K, Nawata H. J Clin Endocrinol Metab; 1996 Feb 23; 81(2):530-5. PubMed ID: 8636263 [Abstract] [Full Text] [Related]
17. Role of sequence variations of the GnRH receptor and G protein-coupled receptor 54 gene in male idiopathic hypogonadotropic hypogonadism. Lanfranco F, Gromoll J, von Eckardstein S, Herding EM, Nieschlag E, Simoni M. Eur J Endocrinol; 2005 Dec 23; 153(6):845-52. PubMed ID: 16322390 [Abstract] [Full Text] [Related]
18. Mutational analysis of the genes encoding RFamide-related peptide-3, the human orthologue of gonadotrophin-inhibitory hormone, and its receptor (GPR147) in patients with gonadotrophin-releasing hormone-dependent pubertal disorders. Lima CJ, Cardoso SC, Lemos EF, Zingler E, Capanema C, Menezes LD, Vogado G, Dos Santos BT, de Moraes OL, Duarte EF, de Brito VN, Latronico AC, Lofrano-Porto A. J Neuroendocrinol; 2014 Nov 23; 26(11):817-24. PubMed ID: 25180599 [Abstract] [Full Text] [Related]
19. Differentiation of male hypogonadotropic hypogonadism and constitutional delay of puberty by pulsatile administration of gonadotropin-releasing hormone. Partsch CJ, Hermanussen M, Sippell WG. J Clin Endocrinol Metab; 1985 Jun 23; 60(6):1196-203. PubMed ID: 3923024 [Abstract] [Full Text] [Related]
20. Mutations of the KISS1 gene in disorders of puberty. Silveira LG, Noel SD, Silveira-Neto AP, Abreu AP, Brito VN, Santos MG, Bianco SD, Kuohung W, Xu S, Gryngarten M, Escobar ME, Arnhold IJ, Mendonca BB, Kaiser UB, Latronico AC. J Clin Endocrinol Metab; 2010 May 23; 95(5):2276-80. PubMed ID: 20237166 [Abstract] [Full Text] [Related] Page: [Next] [New Search]