Xiaoli Wei
Kunming, China
Last Updated: 09/26/2026
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Found 19 publications
CEP131 Deficiency Leads to Multiple Morphological Abnormalities of the Sperm Flagellum-Associated Male Infertility via Impaired CEP290 Interaction.
Journal: Andrology
Published: November 29, 2025
Genetic Underpinnings of Oligoasthenoteratozoospermia.
Journal: Clinical genetics
Published: July 22, 2024
Homozygous mutation in DNALI1 leads to asthenoteratozoospermia by affecting the inner dynein arms.
Journal: Frontiers in endocrinology
Published: September 30, 2022
TENT5D disruption causes oligoasthenoteratozoospermia and male infertility.
Journal: Andrology
Published: August 23, 2022
Tyrosine phosphatase SHP2 in ovarian granulosa cells balances follicular development by inhibiting PI3K/AKT signaling.
Journal: Journal of molecular cell biology
Published: February 28, 2022
Biallelic mutations in ARMC12 cause asthenozoospermia and multiple midpiece defects in humans and mice.
Journal: Journal of medical genetics
Published: August 05, 2021
Biallelic mutations in KATNAL2 cause male infertility due to oligo-astheno-teratozoospermia.
Journal: Clinical genetics
Published: April 27, 2021
Bi-allelic mutations in DNAH7 cause asthenozoospermia by impairing the integrality of axoneme structure.
Journal: Acta biochimica et biophysica Sinica
Published: March 28, 2021
Pathogenic Variants in ACTRT1 Cause Acephalic Spermatozoa Syndrome.
Journal: Frontiers in cell and developmental biology
Published: March 04, 2021
Mutations in ZP4 are associated with abnormal zona pellucida and female infertility.
Journal: Journal of clinical pathology
Published: October 08, 2020
Whole-exome sequencing in patients with premature ovarian insufficiency: early detection and early intervention.
Journal: Journal of ovarian research
Published: June 23, 2020
Last Updated: 09/26/2026