BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

815 related articles for article (PubMed ID: 26911863)

  • 1. 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]  

  • 2. 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]  

  • 3. Novel FSHR variants causing female resistant ovary syndrome.
    Khor S; Lyu Q; Kuang Y; Lu X
    Mol Genet Genomic Med; 2020 Feb; 8(2):e1082. PubMed ID: 31830376
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Novel Inactivating Mutation of the FSH Receptor in Two Siblings of Indian Origin With Premature Ovarian Failure.
    Katari S; Wood-Trageser MA; Jiang H; Kalynchuk E; Muzumdar R; Yatsenko SA; Rajkovic A
    J Clin Endocrinol Metab; 2015 Jun; 100(6):2154-7. PubMed ID: 25875778
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic variations altering FSH action affect circulating hormone levels as well as follicle growth in healthy peripubertal girls.
    Busch AS; Hagen CP; Almstrup K; Main KM; Juul A
    Hum Reprod; 2016 Apr; 31(4):897-904. PubMed ID: 26905078
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A Novel Homozygous Missense FSHR Variant Associated with Hypergonadotropic Hypogonadism in Two Siblings from a Brazilian Family.
    França MM; Lerario AM; Funari MFA; Nishi MY; Narcizo AM; de Mello MP; Guerra-Junior G; Maciel-Guerra AT; Mendonça BB
    Sex Dev; 2017; 11(3):137-142. PubMed ID: 28591755
    [TBL] [Abstract][Full Text] [Related]  

  • 8. FSHB -211 G>T is a major genetic modulator of reproductive physiology and health in childbearing age women.
    Rull K; Grigorova M; Ehrenberg A; Vaas P; Sekavin A; Nõmmemees D; Adler M; Hanson E; Juhanson P; Laan M
    Hum Reprod; 2018 May; 33(5):954-966. PubMed ID: 29617818
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Treatment with human, recombinant FSH improves sperm DNA fragmentation in idiopathic infertile men depending on the FSH receptor polymorphism p.N680S: a pharmacogenetic study.
    Simoni M; Santi D; Negri L; Hoffmann I; Muratori M; Baldi E; Cambi M; Marcou M; Greither T; Baraldi E; Tagliavini S; Carra D; Lombardo F; Gandini L; Pallotti F; Krausz C; Rastrelli G; Ferlin A; Menegazzo M; Pignatti E; Linari F; Marino M; Benaglia R; Levi-Setti PE; Behre HM
    Hum Reprod; 2016 Sep; 31(9):1960-9. PubMed ID: 27329968
    [TBL] [Abstract][Full Text] [Related]  

  • 12. AMH mutations with reduced in vitro bioactivity are related to premature ovarian insufficiency.
    Alvaro Mercadal B; Imbert R; Demeestere I; Gervy C; De Leener A; Englert Y; Costagliola S; Delbaere A
    Hum Reprod; 2015 May; 30(5):1196-202. PubMed ID: 25750103
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A dominant negative mutation at the ATP binding domain of AMHR2 is associated with a defective anti-Müllerian hormone signaling pathway.
    Li L; Zhou X; Wang X; Wang J; Zhang W; Wang B; Cao Y; Kee K
    Mol Hum Reprod; 2016 Sep; 22(9):669-78. PubMed ID: 27430550
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel FSHR mutations in Han Chinese women with sporadic premature ovarian insufficiency.
    Liu H; Guo T; Gong Z; Yu Y; Zhang Y; Zhao S; Qin Y
    Mol Cell Endocrinol; 2019 Jul; 492():110446. PubMed ID: 31077743
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel inactivating mutations in the FSH receptor cause premature ovarian insufficiency with resistant ovary syndrome.
    He WB; Du J; Yang XW; Li W; Tang WL; Dai C; Chen YZ; Zhang YX; Lu GX; Lin G; Gong F; Tan YQ
    Reprod Biomed Online; 2019 Mar; 38(3):397-406. PubMed ID: 30691934
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiency.
    Bestetti I; Barbieri C; Sironi A; Specchia V; Yatsenko SA; De Donno MD; Caslini C; Gentilini D; Crippa M; Larizza L; Marozzi A; Rajkovic A; Toniolo D; Bozzetti MP; Finelli P
    Hum Reprod; 2021 Oct; 36(11):2975-2991. PubMed ID: 34480478
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A Novel mutation in the FSH receptor inhibiting signal transduction and causing primary ovarian failure.
    Doherty E; Pakarinen P; Tiitinen A; Kiilavuori A; Huhtaniemi I; Forrest S; Aittomäki K
    J Clin Endocrinol Metab; 2002 Mar; 87(3):1151-5. PubMed ID: 11889179
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sequence variants of KHDRBS1 as high penetrance susceptibility risks for primary ovarian insufficiency by mis-regulating mRNA alternative splicing.
    Wang B; Li L; Zhu Y; Zhang W; Wang X; Chen B; Li T; Pan H; Wang J; Kee K; Cao Y
    Hum Reprod; 2017 Oct; 32(10):2138-2146. PubMed ID: 28938739
    [TBL] [Abstract][Full Text] [Related]  

  • 19. New mutations in non-syndromic primary ovarian insufficiency patients identified via whole-exome sequencing.
    Patiño LC; Beau I; Carlosama C; Buitrago JC; González R; Suárez CF; Patarroyo MA; Delemer B; Young J; Binart N; Laissue P
    Hum Reprod; 2017 Jul; 32(7):1512-1520. PubMed ID: 28505269
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A homozygous NOBOX truncating variant causes defective transcriptional activation and leads to primary ovarian insufficiency.
    Li L; Wang B; Zhang W; Chen B; Luo M; Wang J; Wang X; Cao Y; Kee K
    Hum Reprod; 2017 Jan; 32(1):248-255. PubMed ID: 27836978
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 41.