BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

178 related articles for article (PubMed ID: 36178483)

  • 41. Whole exome sequencing and trio analysis to broaden the variant spectrum of genes in idiopathic hypogonadotropic hypogonadism.
    Zhang J; Tang SY; Zhu XB; Li P; Lu JQ; Cong JS; Wang LB; Zhang F; Li Z
    Asian J Androl; 2021; 23(3):288-293. PubMed ID: 33208564
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Gonadotropin-releasing hormone, follicle-stimulating hormone beta, luteinizing hormone beta gene structure in idiopathic hypogonadotropic hypogonadism.
    Layman LC; Wilson JT; Huey LO; Lanclos KD; Plouffe L; McDonough PG
    Fertil Steril; 1992 Jan; 57(1):42-9. PubMed ID: 1730329
    [TBL] [Abstract][Full Text] [Related]  

  • 43. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 44. The spectrum of abnormal patterns of gonadotropin-releasing hormone secretion in men with idiopathic hypogonadotropic hypogonadism: clinical and laboratory correlations.
    Spratt DI; Carr DB; Merriam GR; Scully RE; Rao PN; Crowley WF
    J Clin Endocrinol Metab; 1987 Feb; 64(2):283-91. PubMed ID: 3098771
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Prevalence, phenotypic spectrum, and modes of inheritance of gonadotropin-releasing hormone receptor mutations in idiopathic hypogonadotropic hypogonadism.
    Beranova M; Oliveira LM; Bédécarrats GY; Schipani E; Vallejo M; Ammini AC; Quintos JB; Hall JE; Martin KA; Hayes FJ; Pitteloud N; Kaiser UB; Crowley WF; Seminara SB
    J Clin Endocrinol Metab; 2001 Apr; 86(4):1580-8. PubMed ID: 11297587
    [TBL] [Abstract][Full Text] [Related]  

  • 46. An isolated hypogonadotropic hypogonadism male with a novel de novoFGFR1 mutation fathered a normal son evidenced by prenatal genetic diagnosis.
    Xu H; Li Z; Sun T; Chen Y; Wang D; Wang T; Wang S; Liu J
    Andrologia; 2020 Dec; 52(11):e13821. PubMed ID: 32990989
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Complex genetics in idiopathic hypogonadotropic hypogonadism.
    Pitteloud N; Durrani S; Raivio T; Sykiotis GP
    Front Horm Res; 2010; 39():142-153. PubMed ID: 20389092
    [TBL] [Abstract][Full Text] [Related]  

  • 48. The prevalence of intragenic deletions in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
    Pedersen-White JR; Chorich LP; Bick DP; Sherins RJ; Layman LC
    Mol Hum Reprod; 2008 Jun; 14(6):367-70. PubMed ID: 18463157
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism.
    Pitteloud N; Quinton R; Pearce S; Raivio T; Acierno J; Dwyer A; Plummer L; Hughes V; Seminara S; Cheng YZ; Li WP; Maccoll G; Eliseenkova AV; Olsen SK; Ibrahimi OA; Hayes FJ; Boepple P; Hall JE; Bouloux P; Mohammadi M; Crowley W
    J Clin Invest; 2007 Feb; 117(2):457-63. PubMed ID: 17235395
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Congenital idiopathic hypogonadotropic hypogonadism: evidence of defects in the hypothalamus, pituitary, and testes.
    Sykiotis GP; Hoang XH; Avbelj M; Hayes FJ; Thambundit A; Dwyer A; Au M; Plummer L; Crowley WF; Pitteloud N
    J Clin Endocrinol Metab; 2010 Jun; 95(6):3019-27. PubMed ID: 20382682
    [TBL] [Abstract][Full Text] [Related]  

  • 51. The adhesion signaling molecule p190 RhoGAP is required for morphogenetic processes in neural development.
    Brouns MR; Matheson SF; Hu KQ; Delalle I; Caviness VS; Silver J; Bronson RT; Settleman J
    Development; 2000 Nov; 127(22):4891-903. PubMed ID: 11044403
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Update on the Genetics of Idiopathic Hypogonadotropic Hypogonadism.
    Topaloğlu AK
    J Clin Res Pediatr Endocrinol; 2017 Dec; 9(Suppl 2):113-122. PubMed ID: 29280744
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Research on the variants of FGFR1 and CEP290 genes in idiopathic hypogonadotropin hypogonadism.
    Wang SS; Zhao WY; Wu HX; Shu M; Yuan JX; Fang L; Xu C
    Yi Chuan; 2022 Oct; 44(10):937-949. PubMed ID: 36384729
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Genotypic and phenotypic spectra of FGFR1, FGF8, and FGF17 mutations in a Chinese cohort with idiopathic hypogonadotropic hypogonadism.
    Men M; Wu J; Zhao Y; Xing X; Jiang F; Zheng R; Li JD
    Fertil Steril; 2020 Jan; 113(1):158-166. PubMed ID: 31748124
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Characterization of the human nasal embryonic LHRH factor gene, NELF, and a mutation screening among 65 patients with idiopathic hypogonadotropic hypogonadism (IHH).
    Miura K; Acierno JS; Seminara SB
    J Hum Genet; 2004; 49(5):265-8. PubMed ID: 15362570
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Responsiveness to a physiological regimen of GnRH therapy and relation to genotype in women with isolated hypogonadotropic hypogonadism.
    Abel BS; Shaw ND; Brown JM; Adams JM; Alati T; Martin KA; Pitteloud N; Seminara SB; Plummer L; Pignatelli D; Crowley WF; Welt CK; Hall JE
    J Clin Endocrinol Metab; 2013 Feb; 98(2):E206-16. PubMed ID: 23341491
    [TBL] [Abstract][Full Text] [Related]  

  • 57. The GTPase and Rho GAP domains of p190, a tumor suppressor protein that binds the M(r) 120,000 Ras GAP, independently function as anti-Ras tumor suppressors.
    Wang DZ; Nur-E-Kamal MS; Tikoo A; Montague W; Maruta H
    Cancer Res; 1997 Jun; 57(12):2478-84. PubMed ID: 9192829
    [TBL] [Abstract][Full Text] [Related]  

  • 58. 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]  

  • 59. Phenotypic continuum between Waardenburg syndrome and idiopathic hypogonadotropic hypogonadism in humans with SOX10 variants.
    Rojas RA; Kutateladze AA; Plummer L; Stamou M; Keefe DL; Salnikov KB; Delaney A; Hall JE; Sadreyev R; Ji F; Fliers E; Gambosova K; Quinton R; Merino PM; Mericq V; Seminara SB; Crowley WF; Balasubramanian R
    Genet Med; 2021 Apr; 23(4):629-636. PubMed ID: 33442024
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism.
    Kotan LD; Ternier G; Cakir AD; Emeksiz HC; Turan I; Delpouve G; Kardelen AD; Ozcabi B; Isik E; Mengen E; Cakir EDP; Yuksel A; Agladioglu SY; Dilek SO; Evliyaoglu O; Darendeliler F; Gurbuz F; Akkus G; Yuksel B; Giacobini P; Topaloglu AK
    Genet Med; 2021 Jun; 23(6):1008-1016. PubMed ID: 33495532
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.