Literature DB >> 17418157

Mutation analysis of NANOS3 in 80 Chinese and 88 Caucasian women with premature ovarian failure.

Yingying Qin1, Han Zhao, Ertug Kovanci, Joe Leigh Simpson, Zi-Jiang Chen, Aleksandar Rajkovic.   

Abstract

NANOS3 encodes an RNA-binding protein and has a conserved function in germ cell development. Our objective was to investigate whether mutations in NANOS3 were present in Chinese and Caucasian women with premature ovarian failure. A known synonymous single-nucleotide polymorphism (rs 2016163) in exon 1 was identified through sequencing 80 Chinese and 88 Caucasian women with premature ovarian failure. No additional single-nucleotide polymorphisms or mutations were found in exons encoding for NANOS3. Our findings suggest that mutations in NANOS3 exons are rare in both Chinese and Caucasian women with premature ovarian failure.

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Year:  2007        PMID: 17418157      PMCID: PMC2767171          DOI: 10.1016/j.fertnstert.2007.01.020

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


  15 in total

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2.  Disruption of POF1B binding to nonmuscle actin filaments is associated with premature ovarian failure.

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3.  [Follicular stimulating hormone receptor gene C566T mutation in premature ovarian failure].

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4.  Absence of mutations in the coding regions of follicle-stimulating hormone receptor gene in Singapore Chinese women with premature ovarian failure and polycystic ovary syndrome.

Authors:  Y Tong; W X Liao; A C Roy; S C Ng
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9.  Inheritance in idiopathic premature ovarian failure: analysis of 71 cases.

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10.  Incidence of premature ovarian failure.

Authors:  C B Coulam; S C Adamson; J F Annegers
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  11 in total

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Review 2.  Genetics of human female infertility†.

Authors:  Svetlana A Yatsenko; Aleksandar Rajkovic
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Review 6.  Primordial Germ Cell Specification and Migration.

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7.  Mutation analysis of NANOS3 in Brazilian women with primary ovarian failure.

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Journal:  Clinics (Sao Paulo)       Date:  2016-12-01       Impact factor: 2.365

8.  R-spondin2, a novel target of NOBOX: identification of variants in a cohort of women with primary ovarian insufficiency.

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Review 9.  Onco-fertility and personalized testing for potential for loss of ovarian reserve in patients undergoing chemotherapy: proposed next steps for development of genetic testing to predict changes in ovarian reserve.

Authors:  Bei Sun; John Yeh
Journal:  Fertil Res Pract       Date:  2021-06-30

10.  Homozygous inactivating mutation in NANOS3 in two sisters with primary ovarian insufficiency.

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Journal:  Biomed Res Int       Date:  2014-06-26       Impact factor: 3.411

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