BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

497 related articles for article (PubMed ID: 18559922)

  • 21. Homozygous mutation in the prokineticin-receptor2 gene (Val274Asp) presenting as reversible Kallmann syndrome and persistent oligozoospermia: case report.
    Sinisi AA; Asci R; Bellastella G; Maione L; Esposito D; Elefante A; De Bellis A; Bellastella A; Iolascon A
    Hum Reprod; 2008 Oct; 23(10):2380-4. PubMed ID: 18596028
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Kallmann syndrome with a Tyr113His PROKR2 mutation.
    Ha JH; Lee S; Kim Y; Moon JI; Seo J; Jang JH; Cho EH; Kim JM; Rhee BD; Ko KS; Yoo SJ; Won JC
    Medicine (Baltimore); 2017 Sep; 96(35):e7974. PubMed ID: 28858133
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mutation analyses in pedigrees and sporadic cases of ethnic Han Chinese Kallmann syndrome patients.
    Gu WJ; Zhang Q; Wang YQ; Yang GQ; Hong TP; Zhu DL; Yang JK; Ning G; Jin N; Chen K; Zang L; Wang AP; Du J; Wang XL; Yang LJ; Ba JM; Lv ZH; Dou JT; Mu YM
    Exp Biol Med (Maywood); 2015 Nov; 240(11):1480-9. PubMed ID: 26031747
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Biallelic PROKR2 variants and congenital hypogonadotropic hypogonadism: a case report and a literature review.
    Sugisawa C; Taniyama M; Sato T; Takahashi Y; Hasegawa T; Narumi S
    Endocr J; 2022 Jul; 69(7):831-838. PubMed ID: 35236788
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Hypogonadotropic hypogonadism: new aspects in the regulation of hypothalamic-pituitary-gonadal axis].
    Brioude F; Bouvattier CE; Lombès M
    Ann Endocrinol (Paris); 2010 Sep; 71 Suppl 1():S33-41. PubMed ID: 21237329
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Functional Characteristics of Novel FGFR1 Mutations in Patients with Isolated Gonadotropin-Releasing Hormone Deficiency.
    Choi JH; Oh A; Lee Y; Kim GH; Yoo HW
    Exp Clin Endocrinol Diabetes; 2021 Jun; 129(6):457-463. PubMed ID: 32485746
    [TBL] [Abstract][Full Text] [Related]  

  • 27. PROK2/PROKR2 Signaling and Kallmann Syndrome.
    Dodé C; Rondard P
    Front Endocrinol (Lausanne); 2013; 4():19. PubMed ID: 23596439
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The genetic and molecular basis of idiopathic hypogonadotropic hypogonadism.
    Bianco SD; Kaiser UB
    Nat Rev Endocrinol; 2009 Oct; 5(10):569-76. PubMed ID: 19707180
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice.
    Falardeau J; Chung WC; Beenken A; Raivio T; Plummer L; Sidis Y; Jacobson-Dickman EE; Eliseenkova AV; Ma J; Dwyer A; Quinton R; Na S; Hall JE; Huot C; Alois N; Pearce SH; Cole LW; Hughes V; Mohammadi M; Tsai P; Pitteloud N
    J Clin Invest; 2008 Aug; 118(8):2822-31. PubMed ID: 18596921
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Oligogenic basis of isolated gonadotropin-releasing hormone deficiency.
    Sykiotis GP; Plummer L; Hughes VA; Au M; Durrani S; Nayak-Young S; Dwyer AA; Quinton R; Hall JE; Gusella JF; Seminara SB; Crowley WF; Pitteloud N
    Proc Natl Acad Sci U S A; 2010 Aug; 107(34):15140-4. PubMed ID: 20696889
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Triallelic digenic mutation in the prokineticin 2 and GNRH receptor genes in two brothers with normosmic congenital hypogonadotropic hypogonadism.
    Méndez JP; Zenteno JC; Coronel A; Soriano-Ursúa MA; Valencia-Villalvazo EY; Soderlund D; Coral-Vázquez RM; Canto P
    Endocr Res; 2015; 40(3):166-71. PubMed ID: 25531638
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Clinical, hormonal, and genetic characteristics of 25 Chinese patients with idiopathic hypogonadotropic hypogonadism.
    Liu Q; Yin X; Li P
    BMC Endocr Disord; 2022 Jan; 22(1):30. PubMed ID: 35090434
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes.
    Pitteloud N; Meysing A; Quinton R; Acierno JS; Dwyer AA; Plummer L; Fliers E; Boepple P; Hayes F; Seminara S; Hughes VA; Ma J; Bouloux P; Mohammadi M; Crowley WF
    Mol Cell Endocrinol; 2006 Jul; 254-255():60-9. PubMed ID: 16764984
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Functional analysis of the distal region of the third intracellular loop of PROKR2.
    Zhou XT; Chen DN; Xie ZQ; Peng Z; Xia KD; Liu HD; Liu W; Su B; Li JD
    Biochem Biophys Res Commun; 2013 Sep; 439(1):12-7. PubMed ID: 23969157
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterization.
    Quinton R; Duke VM; Robertson A; Kirk JM; Matfin G; de Zoysa PA; Azcona C; MacColl GS; Jacobs HS; Conway GS; Besser M; Stanhope RG; Bouloux PM
    Clin Endocrinol (Oxf); 2001 Aug; 55(2):163-74. PubMed ID: 11531922
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Biased signaling through G-protein-coupled PROKR2 receptors harboring missense mutations.
    Sbai O; Monnier C; Dodé C; Pin JP; Hardelin JP; Rondard P
    FASEB J; 2014 Aug; 28(8):3734-44. PubMed ID: 24830383
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Identification of two novel missense mutations in the KAL1 gene in Han Chinese subjects with Kallmann Syndrome.
    Jap TS; Chiu CY; Lirng JF; Won GS
    J Endocrinol Invest; 2011 Jan; 34(1):53-9. PubMed ID: 20530987
    [TBL] [Abstract][Full Text] [Related]  

  • 38. An ancient founder mutation in PROKR2 impairs human reproduction.
    Avbelj Stefanija M; Jeanpierre M; Sykiotis GP; Young J; Quinton R; Abreu AP; Plummer L; Au MG; Balasubramanian R; Dwyer AA; Florez JC; Cheetham T; Pearce SH; Purushothaman R; Schinzel A; Pugeat M; Jacobson-Dickman EE; Ten S; Latronico AC; Gusella JF; Dode C; Crowley WF; Pitteloud N
    Hum Mol Genet; 2012 Oct; 21(19):4314-24. PubMed ID: 22773735
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Evidence of the importance of the first intracellular loop of prokineticin receptor 2 in receptor function.
    Abreu AP; Noel SD; Xu S; Carroll RS; Latronico AC; Kaiser UB
    Mol Endocrinol; 2012 Aug; 26(8):1417-27. PubMed ID: 22745195
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A genetic basis for functional hypothalamic amenorrhea.
    Caronia LM; Martin C; Welt CK; Sykiotis GP; Quinton R; Thambundit A; Avbelj M; Dhruvakumar S; Plummer L; Hughes VA; Seminara SB; Boepple PA; Sidis Y; Crowley WF; Martin KA; Hall JE; Pitteloud N
    N Engl J Med; 2011 Jan; 364(3):215-25. PubMed ID: 21247312
    [TBL] [Abstract][Full Text] [Related]  

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