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本文引用的文献

1
Mutational screening of FOXO3A and FOXO1A in women with premature ovarian failure.对卵巢早衰女性进行FOXO3A和FOXO1A的突变筛查。
Fertil Steril. 2006 Nov;86(5):1518-21. doi: 10.1016/j.fertnstert.2006.03.054. Epub 2006 Sep 18.
2
Disruption of POF1B binding to nonmuscle actin filaments is associated with premature ovarian failure.POF1B与非肌肉肌动蛋白丝结合的破坏与卵巢早衰有关。
Am J Hum Genet. 2006 Jul;79(1):113-9. doi: 10.1086/505406. Epub 2006 May 26.
3
[Follicular stimulating hormone receptor gene C566T mutation in premature ovarian failure].[卵泡刺激素受体基因C566T突变与卵巢早衰]
Zhonghua Fu Chan Ke Za Zhi. 2006 May;41(5):315-8.
4
The genetic basis of premature ovarian failure.卵巢早衰的遗传基础。
Aust N Z J Obstet Gynaecol. 2006 Jun;46(3):242-4. doi: 10.1111/j.1479-828X.2006.00585.x.
5
X-linked premature ovarian failure: a complex disease.X连锁型卵巢早衰:一种复杂疾病。
Curr Opin Genet Dev. 2006 Jun;16(3):293-300. doi: 10.1016/j.gde.2006.04.005. Epub 2006 May 2.
6
Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure.卵巢早衰患者中GDF9和BMP15的突变及序列变异
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10
A novel 30 bp deletion in the FOXL2 gene in a phenotypically normal woman with primary amenorrhoea: case report.
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80名中国女性和88名白种人卵巢早衰患者中NANOS3的突变分析。

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

作者信息

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

机构信息

Center for Reproductive Medicine, Shandong Provincial Hospital, Shandong University, Jinan, China.

出版信息

Fertil Steril. 2007 Nov;88(5):1465-7. doi: 10.1016/j.fertnstert.2007.01.020. Epub 2007 Apr 5.

DOI:10.1016/j.fertnstert.2007.01.020
PMID:17418157
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2767171/
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.

摘要

NANOS3编码一种RNA结合蛋白,在生殖细胞发育中具有保守功能。我们的目的是调查中国和高加索地区卵巢早衰女性中是否存在NANOS3突变。通过对80名中国卵巢早衰女性和88名高加索卵巢早衰女性进行测序,在第1外显子中鉴定出一个已知的同义单核苷酸多态性(rs 2016163)。在编码NANOS3的外显子中未发现其他单核苷酸多态性或突变。我们的研究结果表明,在患有卵巢早衰的中国和高加索女性中,NANOS3外显子的突变很少见。