BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

310 related articles for article (PubMed ID: 10551778)

  • 1. New natural inactivating mutations of the follicle-stimulating hormone receptor: correlations between receptor function and phenotype.
    Touraine P; Beau I; Gougeon A; Meduri G; Desroches A; Pichard C; Detoeuf M; Paniel B; Prieur M; Zorn JR; Milgrom E; Kuttenn F; Misrahi M
    Mol Endocrinol; 1999 Nov; 13(11):1844-54. PubMed ID: 10551778
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel phenotype related to partial loss of function mutations of the follicle stimulating hormone receptor.
    Beau I; Touraine P; Meduri G; Gougeon A; Desroches A; Matuchansky C; Milgrom E; Kuttenn F; Misrahi M
    J Clin Invest; 1998 Oct; 102(7):1352-9. PubMed ID: 9769327
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Delayed puberty and primary amenorrhea associated with a novel mutation of the human follicle-stimulating hormone receptor: clinical, histological, and molecular studies.
    Meduri G; Touraine P; Beau I; Lahuna O; Desroches A; Vacher-Lavenu MC; Kuttenn F; Misrahi M
    J Clin Endocrinol Metab; 2003 Aug; 88(8):3491-8. PubMed ID: 12915623
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel follicle-stimulating hormone receptor mutation causing primary ovarian failure: a fertility application of whole exome sequencing.
    Bramble MS; Goldstein EH; Lipson A; Ngun T; Eskin A; Gosschalk JE; Roach L; Vashist N; Barseghyan H; Lee E; Arboleda VA; Vaiman D; Yuksel Z; Fellous M; Vilain E
    Hum Reprod; 2016 Apr; 31(4):905-14. PubMed ID: 26911863
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A new FSHbeta mutation in a 29-year-old woman with primary amenorrhea and isolated FSH deficiency: functional characterization and ovarian response to human recombinant FSH.
    Kottler ML; Chou YY; Chabre O; Richard N; Polge C; Brailly-Tabard S; Chanson P; Guiochon-Mantel A; Huhtaniemi I; Young J
    Eur J Endocrinol; 2010 Mar; 162(3):633-41. PubMed ID: 19966036
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Novel Mutation in the FSH Receptor (I423T) Affecting Receptor Activation and Leading to Primary Ovarian Failure.
    Zariñán T; Mayorga J; Jardón-Valadez E; Gutiérrez-Sagal R; Maravillas-Montero JL; Mejía-Domínguez NR; Martínez-Luis I; Yacini-Torres OG; Cravioto MD; Reiter E; Ulloa-Aguirre A
    J Clin Endocrinol Metab; 2021 Jan; 106(2):e534-e550. PubMed ID: 33119067
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel homozygous mutation in the FSHR gene is causative for primary ovarian insufficiency.
    Liu H; Xu X; Han T; Yan L; Cheng L; Qin Y; Liu W; Zhao S; Chen ZJ
    Fertil Steril; 2017 Dec; 108(6):1050-1055.e2. PubMed ID: 29157895
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel loss of function mutation in exon 10 of the FSH receptor gene causing hypergonadotrophic hypogonadism: clinical and molecular characteristics.
    Allen LA; Achermann JC; Pakarinen P; Kotlar TJ; Huhtaniemi IT; Jameson JL; Cheetham TD; Ball SG
    Hum Reprod; 2003 Feb; 18(2):251-6. PubMed ID: 12571157
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Toward gene therapy of primary ovarian failure: adenovirus expressing human FSH receptor corrects the Finnish C566T mutation.
    Ghadami M; Salama SA; Khatoon N; Chilvers R; Nagamani M; Chedrese PJ; Al-Hendy A
    Mol Hum Reprod; 2008 Jan; 14(1):9-15. PubMed ID: 18084009
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular pathology of the FSH receptor: new insights into FSH physiology.
    Meduri G; Bachelot A; Cocca MP; Vasseur C; Rodien P; Kuttenn F; Touraine P; Misrahi M
    Mol Cell Endocrinol; 2008 Jan; 282(1-2):130-42. PubMed ID: 18248882
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor gene.
    Aittomäki K; Herva R; Stenman UH; Juntunen K; Ylöstalo P; Hovatta O; de la Chapelle A
    J Clin Endocrinol Metab; 1996 Oct; 81(10):3722-6. PubMed ID: 8855829
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Successful in vitro maturation of oocytes in a woman with gonadotropin-resistant ovary syndrome associated with a novel combination of FSH receptor gene variants: a case report.
    Flageole C; Toufaily C; Bernard DJ; Ates S; Blais V; Chénier S; Benkhalifa M; Miron P
    J Assist Reprod Genet; 2019 Mar; 36(3):425-432. PubMed ID: 30610662
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Inactivating FSH receptor mutations and gonadal dysfunction.
    Tapanainen JS; Vaskivuo T; Aittomäki K; Huhtaniemi IT
    Mol Cell Endocrinol; 1998 Oct; 145(1-2):129-35. PubMed ID: 9922109
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Poor ovarian response to gonadotropin stimulation is associated with low expression of follicle-stimulating hormone receptor in granulosa cells.
    Cai J; Lou HY; Dong MY; Lu XE; Zhu YM; Gao HJ; Huang HF
    Fertil Steril; 2007 Jun; 87(6):1350-6. PubMed ID: 17296182
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Functional characterization of two naturally occurring mutations (Val514Ala and Ala575Val) in follicle-stimulating hormone receptor.
    Desai SS; Achrekar SK; Sahasrabuddhe KA; Meharji PK; Desai SK; Mangoli VS; Mahale SD
    J Clin Endocrinol Metab; 2015 Apr; 100(4):E638-45. PubMed ID: 25581598
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Toward gene therapy of premature ovarian failure: intraovarian injection of adenovirus expressing human FSH receptor restores folliculogenesis in FSHR(-/-) FORKO mice.
    Ghadami M; El-Demerdash E; Salama SA; Binhazim AA; Archibong AE; Chen X; Ballard BR; Sairam MR; Al-Hendy A
    Mol Hum Reprod; 2010 Apr; 16(4):241-50. PubMed ID: 20086006
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel mutation in exon8 of the follicle-stimulating hormone receptor in a woman with primary amenorrhea.
    Nakamura Y; Maekawa R; Yamagata Y; Tamura I; Sugino N
    Gynecol Endocrinol; 2008 Dec; 24(12):708-12. PubMed ID: 19172541
    [TBL] [Abstract][Full Text] [Related]  

  • 18. An unbalanced translocation unmasks a recessive mutation in the follicle-stimulating hormone receptor (FSHR) gene and causes FSH resistance.
    Kuechler A; Hauffa BP; Köninger A; Kleinau G; Albrecht B; Horsthemke B; Gromoll J
    Eur J Hum Genet; 2010 Jun; 18(6):656-61. PubMed ID: 20087398
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Functional and clinical consequences of mutations in the FSH receptor.
    Gromoll J; Simoni M; Nordhoff V; Behre HM; De Geyter C; Nieschlag E
    Mol Cell Endocrinol; 1996 Dec; 125(1-2):177-82. PubMed ID: 9027356
    [TBL] [Abstract][Full Text] [Related]  

  • 20. In vitro bioassay for human serum follicle-stimulating hormone (FSH) based on L cells transfected with recombinant rat FSH receptor: validation of a model system.
    Gudermann T; Brockmann H; Simoni M; Gromoll J; Nieschlag E
    Endocrinology; 1994 Nov; 135(5):2204-13. PubMed ID: 7956943
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.