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Screening for FOXL2 gene mutations in women with premature ovarian failure: an Indian experience

机译：筛选卵巢过早失效的女性FoxL2基因突变：印度经验

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Suparna Chatterjee; Deepak Modi; Anurupa Maitra; Seema Kadam; Zarine Patel; Jyotsna Gokral; Pervin Meherji;
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年度 2007
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1. Mutational analysis of inhibin alpha gene revealed three novel variations in Indian women with premature ovarian failure. [J] . Prakash GJ, Ravi Kanth VV, Shelling AN, Fertility and Sterility: Official Journal of the American Fertility Society, Pacific Coast Fertility Society, and the Canadian Fertility and Andrology Society . 2010,第1期

机译：抑制素α基因的突变分析揭示了卵巢早衰的印度女性中的三种新颖变异。
2. Mutation analysis of FOXL2 gene in Chinese patients with premature ovarian failure. [J] . Ni F, Wen Q, Wang B, Gynecological endocrinology: the official journal of the International Society of Gynecological Endocrinology . 2010,第4期

机译：中国卵巢早衰患者FOXL2基因的突变分析。
3. Mutant Forkhead L2 (FOXL2) proteins associated with premature ovarian failure (POF) dimerize with wild-type FOXL2, leading to altered regulation of genes associated with granulosa cell differentiation. [J] . Kuo FT, Bentsi Barnes IK, Barlow GM, Endocrinology . 2011,第10期

机译：与卵巢早衰（POF）相关的突变型Forkhead L2（FOXL2）蛋白与野生型FOXL2二聚化，从而导致与颗粒细胞分化相关的基因调控改变。
4. Inactivating Mutation screening of Exon 6 and Exon 10E of FSHR gene in women with Polycystic Ovarian Syndrome in Vellore population [C] . NishuSekar, MadhuraSapre, Vaikhari Kale International Conference on Science, Engineering the Technology . 2018

机译：在瓦雷群中具有多囊卵巢综合征的妇女的外显子6和FSON 10E的突变筛选突变筛选
5. The psychological impact of premature ovarian insufficiency in women with galactosemia: A qualitative study [D] . D'Anna, Kali Nicole 2011

机译：半乳糖虫血症妇女过早卵巢功能不全的心理影响：定性研究
6. Mutant Forkhead L2 (FOXL2) Proteins Associated with Premature Ovarian Failure (POF) Dimerize with Wild-Type FOXL2 Leading to Altered Regulation of Genes Associated with Granulosa Cell Differentiation [O] . Fang-Ting Kuo, Ikuko K. Bentsi-Barnes, Gillian M. Barlow, -1

机译：与卵巢早衰（POF）相关的突变叉头L2（FOXL2）蛋白与野生型FOXL2融合导致与颗粒细胞分化相关基因的调控改变
7. Mutations in the coding region of the FOXL2 gene are not a major cause of idiopathic premature ovarian failure [O] . B. Bodega 2004

机译：FoxL2基因编码区中的突变不是特发性过早卵巢衰竭的主要原因

Screening for FOXL2 gene mutations in women with premature ovarian failure: an Indian experience

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