BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

498 related articles for article (PubMed ID: 20887715)

  • 41. A needle in a haystack: mutations in GNRH1 as a rare cause of isolated GnRH deficiency.
    Chan YM
    Mol Cell Endocrinol; 2011 Oct; 346(1-2):51-6. PubMed ID: 21722705
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Why kisspeptin is such important for reproduction?
    Meczekalski B; Podfigurna-Stopa A; Genazzani AR
    Gynecol Endocrinol; 2011 Jan; 27(1):8-13. PubMed ID: 20672907
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Kisspeptin-54 Accurately Identifies Hypothalamic Gonadotropin-Releasing Hormone Neuronal Dysfunction in Men with Congenital Hypogonadotropic Hypogonadism.
    Abbara A; Eng PC; Phylactou M; Clarke SA; Mills E; Chia G; Yang L; Izzi-Engbeaya C; Smith N; Jayasena CN; Comninos AN; Anand-Ivell R; Rademaker J; Xu C; Quinton R; Pitteloud N; Dhillo WS
    Neuroendocrinology; 2021; 111(12):1176-1186. PubMed ID: 33227799
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Approach to the male patient with congenital hypogonadotropic hypogonadism.
    Young J
    J Clin Endocrinol Metab; 2012 Mar; 97(3):707-18. PubMed ID: 22392951
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Congenital Hypogonadotropic Hypogonadism with Anosmia and Gorlin Features Caused by a PTCH1 Mutation Reveals a New Candidate Gene for Kallmann Syndrome.
    Barraud S; Delemer B; Poirsier-Violle C; Bouligand J; Mérol JC; Grange F; Higel-Chaufour B; Decoudier B; Zalzali M; Dwyer AA; Acierno JS; Pitteloud N; Millar RP; Young J
    Neuroendocrinology; 2021; 111(1-2):99-114. PubMed ID: 32074614
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Neuron-Derived Neurotrophic Factor Is Mutated in Congenital Hypogonadotropic Hypogonadism.
    Messina A; Pulli K; Santini S; Acierno J; Känsäkoski J; Cassatella D; Xu C; Casoni F; Malone SA; Ternier G; Conte D; Sidis Y; Tommiska J; Vaaralahti K; Dwyer A; Gothilf Y; Merlo GR; Santoni F; Niederländer NJ; Giacobini P; Raivio T; Pitteloud N
    Am J Hum Genet; 2020 Jan; 106(1):58-70. PubMed ID: 31883645
    [TBL] [Abstract][Full Text] [Related]  

  • 47. The role of prior pubertal development, biochemical markers of testicular maturation, and genetics in elucidating the phenotypic heterogeneity of idiopathic hypogonadotropic hypogonadism.
    Pitteloud N; Hayes FJ; Boepple PA; DeCruz S; Seminara SB; MacLaughlin DT; Crowley WF
    J Clin Endocrinol Metab; 2002 Jan; 87(1):152-60. PubMed ID: 11788640
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatment.
    Boehm U; Bouloux PM; Dattani MT; de Roux N; Dodé C; Dunkel L; Dwyer AA; Giacobini P; Hardelin JP; Juul A; Maghnie M; Pitteloud N; Prevot V; Raivio T; Tena-Sempere M; Quinton R; Young J
    Nat Rev Endocrinol; 2015 Sep; 11(9):547-64. PubMed ID: 26194704
    [TBL] [Abstract][Full Text] [Related]  

  • 49. 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; 88(6):2730-7. PubMed ID: 12788881
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Isolated familial hypogonadotropic hypogonadism and a GNRH1 mutation.
    Bouligand J; Ghervan C; Tello JA; Brailly-Tabard S; Salenave S; Chanson P; Lombès M; Millar RP; Guiochon-Mantel A; Young J
    N Engl J Med; 2009 Jun; 360(26):2742-8. PubMed ID: 19535795
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Enhanced at puberty 1 (EAP1) is a new transcriptional regulator of the female neuroendocrine reproductive axis.
    Heger S; Mastronardi C; Dissen GA; Lomniczi A; Cabrera R; Roth CL; Jung H; Galimi F; Sippell W; Ojeda SR
    J Clin Invest; 2007 Aug; 117(8):2145-54. PubMed ID: 17627301
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A Novel Gonadotropin-Releasing Hormone 1 (Gnrh1) Enhancer-Derived Noncoding RNA Regulates Gnrh1 Gene Expression in GnRH Neuronal Cell Models.
    Huang PP; Brusman LE; Iyer AK; Webster NJ; Mellon PL
    PLoS One; 2016; 11(7):e0158597. PubMed ID: 27389022
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Gonadotropin-Releasing Hormone Receptor (GnRHR) and Hypogonadotropic Hypogonadism.
    Fanis P; Neocleous V; Papapetrou I; Phylactou LA; Skordis N
    Int J Mol Sci; 2023 Nov; 24(21):. PubMed ID: 37958948
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Molecular genetics of isolated hypogonadotropic hypogonadism and Kallmann syndrome.
    Karges B; Roux N
    Endocr Dev; 2005; 8():67-80. PubMed ID: 15722618
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Congenital Hypogonadotropic Hypogonadism: A Trait Shared by Several Complex Neurodevelopmental Disorders.
    de Roux N; Carel JC; Léger J
    Endocr Dev; 2016; 29():72-86. PubMed ID: 26680573
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Mutation screening of SEMA3A and SEMA7A in patients with congenital hypogonadotropic hypogonadism.
    Känsäkoski J; Fagerholm R; Laitinen EM; Vaaralahti K; Hackman P; Pitteloud N; Raivio T; Tommiska J
    Pediatr Res; 2014 May; 75(5):641-4. PubMed ID: 24522099
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Genetics of isolated hypogonadotropic hypogonadism: role of GnRH receptor and other genes.
    Beate K; Joseph N; Nicolas de R; Wolfram K
    Int J Endocrinol; 2012; 2012():147893. PubMed ID: 22229029
    [TBL] [Abstract][Full Text] [Related]  

  • 58. The gene encoding GnRH and its associated peptide GAP: some insights into hypogonadism.
    Seeburg PH; Mason AJ; Young WS; Stewart TA; Nikolics K
    J Steroid Biochem; 1989 Oct; 33(4B):687-91. PubMed ID: 2689777
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism.
    Pitteloud N; Zhang C; Pignatelli D; Li JD; Raivio T; Cole LW; Plummer L; Jacobson-Dickman EE; Mellon PL; Zhou QY; Crowley WF
    Proc Natl Acad Sci U S A; 2007 Oct; 104(44):17447-52. PubMed ID: 17959774
    [TBL] [Abstract][Full Text] [Related]  

  • 60.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 25.