Author

Caixia Lei

h-index 12 View on Semantic Scholar

We have 2 of 43 papers

We haven’t gathered this author’s papers yet. Follow them and we’ll fetch their work.

Not the right person? Other researchers publish under this name.

Open access Oct 2026

Overexpression of centromere-localized IFIT3 impairs mitochondrial function and disrupts cellular proliferation and cell cycle progression in down syndrome

Down syndrome (DS, trisomy 21) is the most prevalent human autosomal aneuploidy, driven by non-disjunction of chromosome 21 during maternal gametogenesis. Centromere-kinetochore complexes mediate accurate chromosome segregation, and centromeric protein dysregulation is linked to chromosome instability; nevertheless...

Peng Zhou, Yan-Na Liu, Cai-Xia Lei et al. · Frontiers in Genetics · 0 citations

Aug 2026

A Homozygous NUP210L Variant Is Associated With Severe Defects in Human Spermiogenesis.

The findings support a role for NUP210L in human spermiogenesis that is not fully recapitulated in murine models and provide human-based evidence that nucleoporin dysfunction contributes to male infertility.

Yi-Si Sun, Guo-Wu Chen, Yi-Ni Zhang et al. · Andrology · 0 citations