Associated Papers
Heterozygous Eif4nif1 Stop-Gain Mice Replicate the Primary Ovarian Insufficiency Phenotype in Women.
Moriwaki M et al.
Endocrinology, 2025
Genetic insights into the complexity of premature ovarian insufficiency.
Nie L et al.
Reproductive Biology and Endocrinology : Rb&e, 2024
Heterozygous Eif4nif1 Stop Gain Mice Replicate the Primary Ovarian Insufficiency Phenotype in Women.
Moriwaki M et al.
Biorxiv : the Preprint Server for Biology, 2024
Eif4enif1 haploinsufficiency disrupts oocyte mitochondrial dynamics and leads to subfertility.
Ding Y et al.
Development (cambridge, England), 2023
Screening of targeted panel genes in Brazilian patients with primary ovarian insufficiency.
França MM et al.
Plos One, 2020
A novel EIF4ENIF1 mutation associated with a diminished ovarian reserve and premature ovarian insufficiency identified by whole-exome sequencing.
Zhao M et al.
Journal of Ovarian Research, 2019
Mutations in eIF4ENIF1 are associated with primary ovarian insufficiency.
Kasippillai T et al.
The Journal of Clinical Endocrinology and Metabolism, 2013
Genetics of primary ovarian insufficiency: new developments and opportunities.
Qin Y et al.
Human Reproduction Update, 0
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