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
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
Identification of TUBB8 Variants in 5 Primary Infertile Women with Multiple Phenotypes in Oocytes and Early Embryos.
Yu W et al.
Reproductive Sciences (thousand Oaks, Calif.), 2023
Mutation analysis of the TUBB8 gene in primary infertile women with oocyte maturation arrest.
Yao Z et al.
Journal of Ovarian Research, 2022
35354490 (PubMed )
Supplement: 13048_2022_971_MOESM2_ESM.xlsx › novel
Meiosis interrupted: the genetics of female infertility via meiotic failure.
Biswas L et al.
Reproduction (cambridge, England), 2021
Mutation analysis of the TUBB8 gene in primary infertile women with arrest in oocyte maturation.
Wang AC et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology, 2018
Mutation analysis of the TUBB8 gene in nine infertile women with oocyte maturation arrest.
Huang L et al.
Reproductive Biomedicine Online, 2017
Mutations in TUBB8 cause a multiplicity of phenotypes in human oocytes and early embryos.
Feng R et al.
Journal of Medical Genetics, 2016
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