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
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
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
Meiosis interrupted: the genetics of female infertility via meiotic failure.
Biswas L et al.
Reproduction (cambridge, England), 2021
Mutation analysis of tubulin beta 8 class VIII in infertile females with oocyte or embryonic defects.
Yang P et al.
Clinical Genetics, 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
Novel mutations and structural deletions in TUBB8: expanding mutational and phenotypic spectrum of patients with arrest in oocyte maturation, fertilization or early embryonic development.
Chen B et al.
Human Reproduction (oxford, England), 2017
Select a paper to view details