210 related articles for article (PubMed ID: 23329188)
1. Mutational analysis of TAC3 and TACR3 genes in patients with idiopathic central pubertal disorders.
Tusset C; Noel SD; Trarbach EB; Silveira LF; Jorge AA; Brito VN; Cukier P; Seminara SB; Mendonça BB; Kaiser UB; Latronico AC
Arq Bras Endocrinol Metabol; 2012 Dec; 56(9):646-52. PubMed ID: 23329188
[TBL] [Abstract][Full Text] [Related]
2. Association study of TAC3 and TACR3 gene polymorphisms with idiopathic precocious puberty in Chinese girls.
Xin X; Zhang J; Chang Y; Wu Y
J Pediatr Endocrinol Metab; 2015 Jan; 28(1-2):65-71. PubMed ID: 25153567
[TBL] [Abstract][Full Text] [Related]
3. TAC3/TACR3 mutations reveal preferential activation of gonadotropin-releasing hormone release by neurokinin B in neonatal life followed by reversal in adulthood.
Gianetti E; Tusset C; Noel SD; Au MG; Dwyer AA; Hughes VA; Abreu AP; Carroll J; Trarbach E; Silveira LF; Costa EM; de Mendonça BB; de Castro M; Lofrano A; Hall JE; Bolu E; Ozata M; Quinton R; Amory JK; Stewart SE; Arlt W; Cole TR; Crowley WF; Kaiser UB; Latronico AC; Seminara SB
J Clin Endocrinol Metab; 2010 Jun; 95(6):2857-67. PubMed ID: 20332248
[TBL] [Abstract][Full Text] [Related]
4. The role of gene defects underlying isolated hypogonadotropic hypogonadism in patients with constitutional delay of growth and puberty.
Vaaralahti K; Wehkalampi K; Tommiska J; Laitinen EM; Dunkel L; Raivio T
Fertil Steril; 2011 Jun; 95(8):2756-8. PubMed ID: 21292259
[TBL] [Abstract][Full Text] [Related]
5. Mutational analysis of TAC and TACR3 in idiopathic central precocious puberty.
Krstevska-Konstantinova M; Tasic VB; Montenegro LR; Dervisov D; Beneduzzi D; Gontijo Silveira LF; Gucev ZS
Pril (Makedon Akad Nauk Umet Odd Med Nauki); 2014; 35(1):129-32. PubMed ID: 24802197
[TBL] [Abstract][Full Text] [Related]
6. TAC3 and TACR3 defects cause hypothalamic congenital hypogonadotropic hypogonadism in humans.
Young J; Bouligand J; Francou B; Raffin-Sanson ML; Gaillez S; Jeanpierre M; Grynberg M; Kamenicky P; Chanson P; Brailly-Tabard S; Guiochon-Mantel A
J Clin Endocrinol Metab; 2010 May; 95(5):2287-95. PubMed ID: 20194706
[TBL] [Abstract][Full Text] [Related]
7. Role of gonadotropin-releasing hormone receptor mutations in patients with a wide spectrum of pubertal delay.
Beneduzzi D; Trarbach EB; Min L; Jorge AA; Garmes HM; Renk AC; Fichna M; Fichna P; Arantes KA; Costa EM; Zhang A; Adeola O; Wen J; Carroll RS; Mendonça BB; Kaiser UB; Latronico AC; Silveira LF
Fertil Steril; 2014 Sep; 102(3):838-846.e2. PubMed ID: 25016926
[TBL] [Abstract][Full Text] [Related]
8. Normosmic congenital hypogonadotropic hypogonadism due to TAC3/TACR3 mutations: characterization of neuroendocrine phenotypes and novel mutations.
Francou B; Bouligand J; Voican A; Amazit L; Trabado S; Fagart J; Meduri G; Brailly-Tabard S; Chanson P; Lecomte P; Guiochon-Mantel A; Young J
PLoS One; 2011; 6(10):e25614. PubMed ID: 22031817
[TBL] [Abstract][Full Text] [Related]
9. TAC3 and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key role for Neurokinin B in the central control of reproduction.
Topaloglu AK; Reimann F; Guclu M; Yalin AS; Kotan LD; Porter KM; Serin A; Mungan NO; Cook JR; Imamoglu S; Akalin NS; Yuksel B; O'Rahilly S; Semple RK
Nat Genet; 2009 Mar; 41(3):354-358. PubMed ID: 19079066
[TBL] [Abstract][Full Text] [Related]
10. Hypogonadotropic hypogonadism due to a novel missense mutation in the first extracellular loop of the neurokinin B receptor.
Guran T; Tolhurst G; Bereket A; Rocha N; Porter K; Turan S; Gribble FM; Kotan LD; Akcay T; Atay Z; Canan H; Serin A; O'Rahilly S; Reimann F; Semple RK; Topaloglu AK
J Clin Endocrinol Metab; 2009 Oct; 94(10):3633-3639. PubMed ID: 19755480
[TBL] [Abstract][Full Text] [Related]
11. Neurokinin B signalling in human puberty.
Topaloglu AK; Kotan LD; Yuksel B
J Neuroendocrinol; 2010 Jul; 22(7):765-70. PubMed ID: 20456599
[TBL] [Abstract][Full Text] [Related]
12. Prevalence of KISS1 Receptor mutations in a series of 603 patients with normosmic congenital hypogonadotrophic hypogonadism and characterization of novel mutations: a single-centre study.
Francou B; Paul C; Amazit L; Cartes A; Bouvattier C; Albarel F; Maiter D; Chanson P; Trabado S; Brailly-Tabard S; Brue T; Guiochon-Mantel A; Young J; Bouligand J
Hum Reprod; 2016 Jun; 31(6):1363-74. PubMed ID: 27094476
[TBL] [Abstract][Full Text] [Related]
13. Hypothalamic dysfunction in a female with isolated hypogonadotropic hypogonadism and compound heterozygous TACR3 mutations and clinical manifestation in her heterozygous mother.
Fukami M; Maruyama T; Dateki S; Sato N; Yoshimura Y; Ogata T
Horm Res Paediatr; 2010; 73(6):477-81. PubMed ID: 20395662
[TBL] [Abstract][Full Text] [Related]
14. Distribution of gene mutations associated with familial normosmic idiopathic hypogonadotropic hypogonadism.
Gürbüz F; Kotan LD; Mengen E; Şıklar Z; Berberoğlu M; Dökmetaş S; Kılıçlı MF; Güven A; Kirel B; Saka N; Poyrazoğlu Ş; Cesur Y; Doğan M; Özen S; Özbek MN; Demirbilek H; Kekil MB; Temiz F; Önenli Mungan N; Yüksel B; Topaloğlu AK
J Clin Res Pediatr Endocrinol; 2012 Sep; 4(3):121-6. PubMed ID: 22766261
[TBL] [Abstract][Full Text] [Related]
15. 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; 95(5):2276-80. PubMed ID: 20237166
[TBL] [Abstract][Full Text] [Related]
16. 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; 26(11):817-24. PubMed ID: 25180599
[TBL] [Abstract][Full Text] [Related]
17. Molecular causes of hypogonadotropic hypogonadism.
Topaloglu AK; Kotan LD
Curr Opin Obstet Gynecol; 2010 Aug; 22(4):264-70. PubMed ID: 20543690
[TBL] [Abstract][Full Text] [Related]
18. Delayed and Precocious Puberty: Genetic Underpinnings and Treatments.
Gohil A; Eugster EA
Endocrinol Metab Clin North Am; 2020 Dec; 49(4):741-757. PubMed ID: 33153677
[TBL] [Abstract][Full Text] [Related]
19. A shared genetic basis for self-limited delayed puberty and idiopathic hypogonadotropic hypogonadism.
Zhu J; Choa RE; Guo MH; Plummer L; Buck C; Palmert MR; Hirschhorn JN; Seminara SB; Chan YM
J Clin Endocrinol Metab; 2015 Apr; 100(4):E646-54. PubMed ID: 25636053
[TBL] [Abstract][Full Text] [Related]
20. Genetics basis for GnRH-dependent pubertal disorders in humans.
Silveira LF; Trarbach EB; Latronico AC
Mol Cell Endocrinol; 2010 Aug; 324(1-2):30-8. PubMed ID: 20188792
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
