Yiyuan Liu
Hefei, 230032, China
Last Updated: 09/26/2026
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Found 8 publications
Novel mutations in DNAH17 cause sperm flagellum defects and their influence on ICSI outcome.
Journal: Journal of assisted reproduction and genetics
Published: April 04, 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
Bi-allelic human TEKT3 mutations cause male infertility with oligoasthenoteratozoospermia owing to acrosomal hypoplasia and reduced progressive motility.
Journal: Human molecular genetics
Published: October 12, 2022
DNALI1 deficiency causes male infertility with severe asthenozoospermia in humans and mice by disrupting the assembly of the flagellar inner dynein arms and fibrous sheath.
Journal: Cell death & disease
Published: August 31, 2022
Homozygous missense mutation in CCDC155 disrupts the transmembrane distribution of CCDC155 and SUN1, resulting in non-obstructive azoospermia and premature ovarian insufficiency in humans.
Journal: Human genetics
Published: February 18, 2022
Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformations.
Journal: Reproductive biology and endocrinology : RB&E
Published: August 25, 2021
A homozygous loss-of-function mutation in FBXO43 causes human non-obstructive azoospermia.
Journal: Clinical genetics
Published: August 11, 2021
Showing 1-8 of 8
Last Updated: 09/26/2026