Associated Papers
Genetic landscape of human oocyte/embryo defects.
Chen B et al.
Cell Genomics, 2026
41005306 (PubMed )
Supplement: mmc3.xlsx › Table_S2
Advances in monogenic female infertility.
Gu H et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao, 2025
The maternal protein NLRP5 stabilizes UHRF1 in the cytoplasm: implication for the pathogenesis of multilocus imprinting disturbance.
Unoki M et al.
Human Molecular Genetics, 2024
38868925 (PubMed )
Supplement: sup_info_hmg_unoki_060424_ddae096.pdf
Genetic variants underlying developmental arrests in human preimplantation embryos.
Ozturk S
Molecular Human Reproduction, 2023
Gene mutations impede oocyte maturation, fertilization, and early embryonic development.
Fei CF et al.
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology, 2022
Novel mutations in NLRP5 and PATL2 cause female infertility characterized by primarily oocyte maturation abnormality and consequent early embryonic arrest.
Huang L et al.
Journal of Assisted Reproduction and Genetics, 2022
DNA Methylation Dynamics in the Female Germline and Maternal-Effect Mutations That Disrupt Genomic Imprinting.
Anvar Z et al.
Genes, 2021
A novel homozygous variant in NLRP5 is associate with human early embryonic arrest in a consanguineous Chinese family.
Xu Y et al.
Clinical Genetics, 2020
Mutations in NLRP2 and NLRP5 cause female infertility characterised by early embryonic arrest.
Mu J et al.
Journal of Medical Genetics, 2019
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