Hua-lin Huang
No. 139, Renmin Middle Road
Changsha, 410011, China
Changsha, 410011, China
Last Updated: 09/26/2026
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Found 8 publications
CKAP5 deficiency induces premature ovarian insufficiency.
Journal: EBioMedicine
Published: October 31, 2024
A new genetic diagnosis strategy for paroxysmal kinesigenic dyskinesia: Targeted high-throughput detection of PRRT2 gene c.649 locus.
Journal: Molecular genetics & genomic medicine
Published: February 22, 2024
Identification of zona pellucida defects revealed a novel loss-of-function mutation in ZP2 in humans and rats.
Journal: Frontiers in endocrinology
Published: February 19, 2023
A novel frameshift mutation in DNAH6 associated with male infertility and asthenoteratozoospermia.
Journal: Frontiers in endocrinology
Published: December 12, 2022
A novel compound heterozygous mutation in TUBB8 causing early embryonic developmental arrest.
Journal: Journal of assisted reproduction and genetics
Published: November 17, 2022
Mutant Zp1 impedes incorporation of ZP3 and ZP4 in the zona pellucida, resulting in zona absence and female infertility in rats†.
Journal: Biology of reproduction
Published: May 05, 2020
Zp4 is completely dispensable for fertility in female rats†.
Journal: Biology of reproduction
Published: February 25, 2020
Influence of mouse defective zona pellucida in folliculogenesis on apoptosis of granulosa cells and developmental competence of oocytes†.
Journal: Biology of reproduction
Published: September 26, 2018
Showing 1-8 of 8
Last Updated: 09/26/2026