BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

182 related articles for article (PubMed ID: 21292259)

  • 1. 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]  

  • 2. Isolated cryptorchidism: no evidence for involvement of genes underlying isolated hypogonadotropic hypogonadism.
    Laitinen EM; Tommiska J; Virtanen HE; Oehlandt H; Koivu R; Vaaralahti K; Toppari J; Raivio T
    Mol Cell Endocrinol; 2011 Jul; 341(1-2):35-8. PubMed ID: 21664240
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. The genetics of hypogonadotropic hypogonadism.
    Bhagavath B; Layman LC
    Semin Reprod Med; 2007 Jul; 25(4):272-86. PubMed ID: 17594608
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Genetics of congenital hypogonadotropic hypogonadism in Denmark.
    Tommiska J; Känsäkoski J; Christiansen P; Jørgensen N; Lawaetz JG; Juul A; Raivio T
    Eur J Med Genet; 2014 Jul; 57(7):345-8. PubMed ID: 24732674
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Reversible congenital hypogonadotropic hypogonadism in patients with CHD7, FGFR1 or GNRHR mutations.
    Laitinen EM; Tommiska J; Sane T; Vaaralahti K; Toppari J; Raivio T
    PLoS One; 2012; 7(6):e39450. PubMed ID: 22724017
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Hypogonadotropic hypogonadism.
    Layman LC
    Endocrinol Metab Clin North Am; 2007 Jun; 36(2):283-96. PubMed ID: 17543719
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A homozygous R262Q mutation in the gonadotropin-releasing hormone receptor presenting as constitutional delay of growth and puberty with subsequent borderline oligospermia.
    Lin L; Conway GS; Hill NR; Dattani MT; Hindmarsh PC; Achermann JC
    J Clin Endocrinol Metab; 2006 Dec; 91(12):5117-21. PubMed ID: 16968799
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1.
    Trarbach EB; Teles MG; Costa EM; Abreu AP; Garmes HM; Guerra G; Baptista MT; de Castro M; Mendonca BB; Latronico AC
    Clin Endocrinol (Oxf); 2010 Mar; 72(3):371-6. PubMed ID: 19489874
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Molecular defects of the GnRH-receptor gene in Chinese patients with idiopathic hypogonadotropic hypogonadism and the severity of hypogonadism.
    Fathi AK; Hu S; Fu X; Huang S; Liang Y; Ning Q; Luo X
    J Pediatr Endocrinol Metab; 2012; 25(7-8):659-68. PubMed ID: 23155690
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations.
    Akkuş G; Kotan LD; Durmaz E; Mengen E; Turan İ; Ulubay A; Gürbüz F; Yüksel B; Tetiker T; Topaloğlu AK
    J Clin Res Pediatr Endocrinol; 2017 Jun; 9(2):95-100. PubMed ID: 28008864
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Paediatric phenotype of Kallmann syndrome due to mutations of fibroblast growth factor receptor 1 (FGFR1).
    Zenaty D; Bretones P; Lambe C; Guemas I; David M; Léger J; de Roux N
    Mol Cell Endocrinol; 2006 Jul; 254-255():78-83. PubMed ID: 16757108
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The prevalence of gonadotropin-releasing hormone receptor mutations in a large cohort of patients with hypogonadotropic hypogonadism.
    Bhagavath B; Ozata M; Ozdemir IC; Bolu E; Bick DP; Sherins RJ; Layman LC
    Fertil Steril; 2005 Oct; 84(4):951-7. PubMed ID: 16213849
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.