Associated Papers
Genetic landscape of human oocyte/embryo defects.
Chen B et al.
Cell Genomics, 2026
41005306 (PubMed )
Supplement: mmc3.xlsx › Table_S2
Identification of novel variants and expansion of the phenotypic spectrum in PATL2, WEE2, and TUBB8 associated with human early embryonic arrest.
Zhao H et al.
Journal of Assisted Reproduction and Genetics, 2025
R391 human dominant mutation does not affect TubB4b localization and sensory hair cells structure in zebrafish inner ear and lateral line.
Smaili W et al.
Developmental Biology, 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
Exonic genetic variants associated with unexpected fertilization failure and zygotic arrest after ICSI: a systematic review.
Torra-Massana M et al.
Zygote (cambridge, England), 2023
Genetic variants underlying developmental arrests in human preimplantation embryos.
Ozturk S
Molecular Human Reproduction, 2023
The comprehensive variant and phenotypic spectrum of TUBB8 in female infertility.
Zheng W et al.
Journal of Assisted Reproduction and Genetics, 2021
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
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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