Associated Papers
Advances in monogenic female infertility.
Gu H et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao, 2025
Genetic insights into the complexity of premature ovarian insufficiency.
Nie L et al.
Reproductive Biology and Endocrinology : Rb&e, 2024
Selected Genetic Factors Associated with Primary Ovarian Insufficiency.
Chen M et al.
International Journal of Molecular Sciences, 2023
The Genetics of Non-Syndromic Primary Ovarian Insufficiency: A Systematic Review.
Venturella R et al.
International Journal of Fertility & Sterility, 2019
Clonal evolution patterns in acute myeloid leukemia with NPM1 mutation.
Cocciardi S et al.
Nature Communications, 2019
31048683 (PubMed )
Supplement: 41467_2019_9745_MOESM4_ESM.xlsx › Tabelle1
PUM1 and PUM2 exhibit different modes of regulation for SIAH1 that involve cooperativity with NANOS paralogues.
Sajek M et al.
Cellular and Molecular Life Sciences : Cmls, 2019
Mutation analysis of NANOS3 in Brazilian women with primary ovarian failure.
Sousa BL et al.
Clinics (sao Paulo, Brazil), 2016
Aetiological coding sequence variants in non-syndromic premature ovarian failure: From genetic linkage analysis to next generation sequencing.
Laissue P
Molecular and Cellular Endocrinology, 2015
Homozygous inactivating mutation in NANOS3 in two sisters with primary ovarian insufficiency.
Santos MG et al.
Biomed Research International, 2014
A NANOS3 mutation linked to protein degradation causes premature ovarian insufficiency.
Wu X et al.
Cell Death & Disease, 2013
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