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Journal Abstract Search

168 related items for PubMed ID: 7641904

  • 1. The follicle-stimulating hormone receptor gene is polymorphic in premature ovarian failure and normal controls.
    Whitney EA, Layman LC, Chan PJ, Lee A, Peak DB, McDonough PG.
    Fertil Steril; 1995 Sep; 64(3):518-24. PubMed ID: 7641904
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  • 5. Follicle-stimulating hormone receptor gene mutations are rare in Japanese women with premature ovarian failure and polycystic ovary syndrome.
    Takakura K, Takebayashi K, Wang HQ, Kimura F, Kasahara K, Noda Y.
    Fertil Steril; 2001 Jan; 75(1):207-9. PubMed ID: 11163840
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  • 7. [Follicular stimulating hormone receptor gene C566T mutation in premature ovarian failure].
    Chen XN, Chen GA, Li MZ.
    Zhonghua Fu Chan Ke Za Zhi; 2006 May; 41(5):315-8. PubMed ID: 16762186
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  • 8. Screening of follicle-stimulating hormone receptor gene in women with premature ovarian failure in southern Brazil and associations with phenotype.
    Vilodre LC, Kohek MB, Spritzer PM.
    J Endocrinol Invest; 2008 Jun; 31(6):552-7. PubMed ID: 18591890
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  • 9. Mutation screening and isoform prevalence of the follicle stimulating hormone receptor gene in women with premature ovarian failure, resistant ovary syndrome and polycystic ovary syndrome.
    Conway GS, Conway E, Walker C, Hoppner W, Gromoll J, Simoni M.
    Clin Endocrinol (Oxf); 1999 Jul; 51(1):97-9. PubMed ID: 10468971
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  • 11. The use of denaturing gradient gel electrophoresis to screen for DNA sequence polymorphisms in the human factor VIII gene.
    Collins M, Wolf SF, Haines LL, Mitsock L.
    Electrophoresis; 1989 Jul; 10(5-6):390-6. PubMed ID: 2569966
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  • 13. Screening of FSH receptor gene in Argentine women with premature ovarian failure (POF).
    Sundblad V, Chiauzzi VA, Escobar ME, Dain L, Charreau EH.
    Mol Cell Endocrinol; 2004 Jul 30; 222(1-2):53-9. PubMed ID: 15249125
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  • 14. Mutation analysis of the gonadotropin-releasing hormone receptor gene in idiopathic hypogonadotropic hypogonadism.
    Layman LC, Peak DB, Xie J, Sohn SH, Reindollar RH, Gray MR.
    Fertil Steril; 1997 Dec 30; 68(6):1079-85. PubMed ID: 9418701
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  • 15. Single nucleotide polymorphisms in premature ovarian failure-associated genes in a Chinese Hui population.
    Ma L, Chen Y, Mei S, Liu C, Ma X, Li Y, Jiang Y, Ha L, Xu X.
    Mol Med Rep; 2015 Aug 30; 12(2):2529-38. PubMed ID: 25954833
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  • 16. Identification of allelic variants in the follicle-stimulating hormone receptor genes of females with or without hypergonadotropic amenorrhea.
    Liu JY, Gromoll J, Cedars MI, La Barbera AR.
    Fertil Steril; 1998 Aug 30; 70(2):326-31. PubMed ID: 9696229
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  • 17. Use of denaturing gradient gel blots to screen for point mutations in the factor VIII gene.
    Laprise SL, Mak EK, Killoran KA, Layman LC, Gray MR.
    Hum Mutat; 1998 Aug 30; 12(6):393-402. PubMed ID: 9829908
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  • 18. 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 30; 15(12):2644-9. PubMed ID: 11098038
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  • 19. FSH receptor gene variants are rarely associated with premature ovarian failure.
    Woad KJ, Prendergast D, Winship IM, Shelling AN.
    Reprod Biomed Online; 2013 Apr 30; 26(4):396-9. PubMed ID: 23419799
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  • 20. 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 30; 105(3):265-6. PubMed ID: 19339009
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