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 the genetic etiology of female infertility.
Gu R et al.
Journal of Assisted Reproduction and Genetics, 2024
A novel heterozygous missense variant of PANX1 causes human oocyte death and female infertility.
Zhou J et al.
Journal of Ovarian Research, 2024
A novel heterozygous variant in PANX1 causes primary infertility due to oocyte death.
Zhou J et al.
Journal of Assisted Reproduction and Genetics, 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
A novel heterozygous variant in PANX1 is associated with oocyte death and female infertility.
Wu XW et al.
Journal of Assisted Reproduction and Genetics, 2022
Homozygous variants in PANX1 cause human oocyte death and female infertility.
Wang W et al.
European Journal of Human Genetics : Ejhg, 2021
Pannexin 1 Transgenic Mice: Human Diseases and Sleep-Wake Function Revision.
Battulin N et al.
International Journal of Molecular Sciences, 2021
Mutational effects of Pannexin 1 R217H depend on the carboxyl-terminus.
Purohit R et al.
Biochemical and Biophysical Research Communications, 2021
Pannexin 1 mutation found in melanoma tumor reduces phosphorylation, glycosylation, and trafficking of the channel-forming protein.
Nouri-Nejad D et al.
Molecular Biology of the Cell, 2021
Molecular genetics of infertility: loss-of-function mutations in humans and corresponding knockout/mutated mice.
Jiao SY et al.
Human Reproduction Update, 2021
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