Xuan Sha
Hefei, 230022, China
Last Updated: 09/26/2026
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Found 9 publications
Genetic variants in diminished ovarian reserve and premature ovarian insufficiency: implications for assisted reproductive outcomes.
Journal: Journal of assisted reproduction and genetics
Published: April 11, 2025
Two compound heterozygous MEIOSIN (likely) pathogenic variants cause female infertility with premature ovarian insufficiency through the disruption of meiosis-related gene transcription.
Journal: Journal of ovarian research
Published: March 31, 2025
A Novel Compound Heterozygous Mutation in TEX14 Causes Human Non-Obstructive Azoospermia by Disrupting the Assembly of Intercellular Bridges.
Journal: Clinical genetics
Published: February 19, 2025
Novel homozygous variants in piRNA pathway factors lead to male infertility in humans.
Journal: Reproductive biomedicine online
Published: June 17, 2024
CALR3 defects disrupt sperm-zona pellucida binding in humans: new insights into male factor fertilization failure and relevant clinical therapeutic approaches.
Journal: Human reproduction (Oxford, England)
Published: March 26, 2024
Adenylate kinase phosphate energy shuttle underlies energetic communication in flagellar axonemes.
Journal: Science China. Life sciences
Published: November 21, 2023
ACROSIN deficiency causes total fertilization failure in humans by preventing the sperm from penetrating the zona pellucida.
Journal: Human reproduction (Oxford, England)
Published: January 09, 2023
Showing 1-9 of 9
Last Updated: 09/26/2026