Tongyao Hu
NHC Key Laboratory Of Human Stem Cell And Reproductive Engineering
Changsha, 410083, China
Changsha, 410083, China
Last Updated: 09/26/2026
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Found 8 publications
A common cause of non-obstructive azoospermia: biallelic MEI1 variants and implications for infertility diagnostics.
Journal: Journal of assisted reproduction and genetics
Published: November 10, 2025
The landscape of RNA binding proteins in mammalian spermatogenesis.
Journal: Science (New York, N.Y.)
Published: August 29, 2024
Novel homozygous variants in TTC12 cause male infertility with asthenoteratozoospermia owing to dynein arm complex and mitochondrial sheath defects in flagella.
Journal: Frontiers in cell and developmental biology
Published: March 11, 2023
Biallelic CFAP61 variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia.
Journal: Journal of medical genetics
Published: September 30, 2021
Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice.
Journal: American journal of human genetics
Published: September 03, 2021
CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesis.
Journal: Human molecular genetics
Published: March 23, 2021
Genetic underpinnings of asthenozoospermia.
Journal: Best practice & research. Clinical endocrinology & metabolism
Published: November 16, 2020
Showing 1-8 of 8
Last Updated: 09/26/2026