Associated Papers
Genetic landscape of human oocyte/embryo defects.
Chen B et al.
Cell Genomics, 2026
41005306 (PubMed )
Supplement: mmc3.xlsx › Table_S2
Molecular Guardians of Oocyte Maturation: A Systematic Review on TUBB8, KIF11, and CKAP5 in IVF Outcomes.
Voros C et al.
International Journal of Molecular Sciences, 2025
Testing the role of unstimulated in vitro maturation for potential development of immature oocytes in women with oocyte maturation abnormalities
Kalyoncu Ş et al.
Journal of the Turkish German Gynecological Association, 2024
Novel variants in TUBB8 gene cause multiple phenotypic abnormalities in human oocytes and early embryos.
Hu T et al.
Journal of Ovarian Research, 2023
TUBB8 mutations as a cause of oocyte maturation abnormalities: presentation of oocyte and embryo profiles and novel mutations.
Ebru H et al.
Reproductive Biomedicine Online, 2023
Genetic variants underlying developmental arrests in human preimplantation embryos.
Ozturk S
Molecular Human Reproduction, 2023
A novel compound heterozygous mutation in TUBB8 causing early embryonic developmental arrest.
Zhang J et al.
Journal of Assisted Reproduction and Genetics, 2023
Meiosis interrupted: the genetics of female infertility via meiotic failure.
Biswas L et al.
Reproduction (cambridge, England), 2021
Identification novel mutations in TUBB8 in female infertility and a novel phenotype of large polar body in oocytes with TUBB8 mutations.
Zhao L et al.
Journal of Assisted Reproduction and Genetics, 2020
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