Literature DB >> 6628716

Evidence for a genetic factor in the etiology of premature ovarian failure.

C B Coulam, S Stringfellow, D Hoefnagel.   

Abstract

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Year:  1983        PMID： 6628716     DOI： 10.1016/s0015-0282(16)47433-9

Source DB:  PubMed          Journal:  Fertil Steril        ISSN： 0015-0282            Impact factor:   7.329


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  9 in total

1.  Association between estrogen receptora gene (ESR1) PvuII (T/C) and XbaI (A/G) polymorphisms and premature ovarian failure risk: evidence from a meta-analysis.

Authors:  Meirong He; Jingcheng Shu; Xing Huang; Hui Tang
Journal:  J Assist Reprod Genet       Date:  2014-11-27       Impact factor: 3.412

2.  Genomic analysis using high-resolution single-nucleotide polymorphism arrays reveals novel microdeletions associated with premature ovarian failure.

Authors:  Megan M McGuire; Wayne Bowden; Natalie J Engel; Hyo Won Ahn; Ertug Kovanci; Aleksandar Rajkovic
Journal:  Fertil Steril       Date:  2011-01-22       Impact factor: 7.329

3.  Screening of follicle-stimulating hormone receptor gene in women with premature ovarian failure in southern Brazil and associations with phenotype.

Authors:  L C Vilodre; M B F Kohek; P M Spritzer
Journal:  J Endocrinol Invest       Date:  2008-06       Impact factor: 4.256

4.  Familial premature ovarian failure.

Authors:  D R Mattison; M I Evans; W B Schwimmer; B J White; B Jensen; J D Schulman
Journal:  Am J Hum Genet       Date:  1984-11       Impact factor: 11.025

5.  Mutations in NR5A1 associated with ovarian insufficiency.

Authors:  Diana Lourenço; Raja Brauner; Lin Lin; Arantzazu De Perdigo; Georges Weryha; Mihaela Muresan; Radia Boudjenah; Gil Guerra-Junior; Andréa T Maciel-Guerra; John C Achermann; Ken McElreavey; Anu Bashamboo
Journal:  N Engl J Med       Date:  2009-02-25       Impact factor: 91.245

6.  Epigenetic control of the critical region for premature ovarian failure on autosomal genes translocated to the X chromosome: a hypothesis.

Authors:  Flavio Rizzolio; Cinzia Sala; Simone Alboresi; Silvia Bione; Serena Gilli; Mara Goegan; Tiziano Pramparo; Orsetta Zuffardi; Daniela Toniolo
Journal:  Hum Genet       Date:  2007-01-31       Impact factor: 4.132

7.  Aod2, the locus controlling development of atrophy in neonatal thymectomy-induced autoimmune ovarian dysgenesis, co-localizes with Il2, Fgfb, and Idd3.

Authors:  C Teuscher; B B Wardell; J K Lunceford; S D Michael; K S Tung
Journal:  J Exp Med       Date:  1996-02-01       Impact factor: 14.307

8.  Distribution of FMR1 and FMR2 Repeats in Argentinean Patients with Primary Ovarian Insufficiency.

Authors:  Lucía Daniela Espeche; Violeta Chiauzzi; Ianina Ferder; Mehrnoosh Arrar; Andrea Paula Solari; Carlos David Bruque; Marisol Delea; Susana Belli; Cecilia Soledad Fernández; Noemí Delia Buzzalino; Eduardo Hernán Charreau; Liliana Beatriz Dain
Journal:  Genes (Basel)       Date:  2017-08-16       Impact factor: 4.096

9.  Investigation of KIT gene mutations in women with 46,XX spontaneous premature ovarian failure.

Authors:  Kyoko Shibanuma; Zhi-Bin Tong; Vien H Vanderhoof; Konstantina Vanevski; Lawrence M Nelson
Journal:  BMC Womens Health       Date:  2002-08-02       Impact factor: 2.809
  9 in total

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