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Journal Abstract Search

128 related items for PubMed ID: 9757892

  • 21.
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  • 23. 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
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  • 24. 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
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  • 25. Absence of 566C>T mutation in exon 7 of the FSHR gene in Indian women with premature ovarian failure.
    Prakash GJ, Kanth VV, Shelling AN, Rozati R, Sujatha M.
    Int J Gynaecol Obstet; 2009 Jun; 105(3):265-6. PubMed ID: 19339009
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  • 26. Inhibin: a candidate gene for premature ovarian failure.
    Shelling AN, Burton KA, Chand AL, van Ee CC, France JT, Farquhar CM, Milsom SR, Love DR, Gersak K, Aittomäki K, Winship IM.
    Hum Reprod; 2000 Dec; 15(12):2644-9. PubMed ID: 11098038
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  • 29. Estrogen receptor alpha gene polymorphisms are associated with idiopathic premature ovarian failure.
    Bretherick KL, Hanna CW, Currie LM, Fluker MR, Hammond GL, Robinson WP.
    Fertil Steril; 2008 Feb; 89(2):318-24. PubMed ID: 17706202
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  • 31. No evidence of somatic activating mutations on gonadotropin receptor genes in sex cord stromal tumors.
    Giacaglia LR, Kohek MB da F, Carvalho FM, Fragoso MC, Mendonca B, Latronico AC.
    Fertil Steril; 2000 Nov; 74(5):992-5. PubMed ID: 11056247
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  • 33. [Application of DHPLC screening TGFBR-3 gene in Chinese women with idiopathic premature ovarian failure].
    Qin CR, Yao JL, Yuan Z, Zhu WJ, Xie JS, Wu WQ.
    Zhonghua Fu Chan Ke Za Zhi; 2013 Jun; 48(6):432-6. PubMed ID: 24103122
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  • 34. Application of Chinese hamster ovary cells transfected with the recombinant human follicle-stimulating hormone (FSH) receptor for measurement of serum FSH.
    Tano M, Minegishi T, Nakamura K, Karino S, Ibuki Y.
    Fertil Steril; 1995 Dec; 64(6):1120-4. PubMed ID: 7589663
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  • 36. BMP15 mutations in XX gonadal dysgenesis and premature ovarian failure.
    Ledig S, Röpke A, Haeusler G, Hinney B, Wieacker P.
    Am J Obstet Gynecol; 2008 Jan; 198(1):84.e1-5. PubMed ID: 17826728
    [Abstract] [Full Text] [Related]

  • 37. The CC-allele of the PvuII polymorphic variant in intron 1 of the α-estrogen receptor gene is significantly more prevalent among infertile women at risk of premature ovarian aging.
    M'Rabet N, Moffat R, Helbling S, Kaech A, Zhang H, de Geyter C.
    Fertil Steril; 2012 Oct; 98(4):965-72.e1-5. PubMed ID: 22749220
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  • 38. Pregnancies after oocyte donation in women with ovarian failure caused by an inactivating mutation in the follicle stimulating hormone receptor.
    Hovatta O, Söderström-Anttila V, Foudila T, Tuomivaara L, Juntunen K, Tiitinen A, Aittomäki K.
    Hum Reprod; 2002 Jan; 17(1):124-7. PubMed ID: 11756374
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  • 39. Relationship of estradiol and inhibin to the follicle-stimulating hormone variability in hypergonadotropic hypogonadism or premature ovarian failure.
    Welt CK, Hall JE, Adams JM, Taylor AE.
    J Clin Endocrinol Metab; 2005 Feb; 90(2):826-30. PubMed ID: 15562017
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  • 40. Adiponectin gene polymorphisms may not be associated with idiopathic premature ovarian failure.
    Ye Y, Pu D, Liu J, Li F, Cui Y, Wu J.
    Gene; 2013 Apr 15; 518(2):262-6. PubMed ID: 23370338
    [Abstract] [Full Text] [Related]

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