Yiling Zhou

Shanghai, 200030, China

Last Updated: 09/26/2026

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Found 14 publications

CFAP251 Deficiency Induces Male Infertility and PCD-like Ciliary Defects by Disrupting TUBB4B and SLC25A4 Recruitment in Humans and Mice.

CFAP251 Deficiency Induces Male Infertility and PCD-like Ciliary Defects by Disrupting TUBB4B and SLC25A4 Recruitment in Humans and Mice.

Journal: International journal of biological sciences

Published: November 22, 2025

Deficiency of primate-specific TFDP3 causes male infertility with oligoasthenoteratozoospermia in humans and cynomolgus monkeys.

Deficiency of primate-specific TFDP3 causes male infertility with oligoasthenoteratozoospermia in humans and cynomolgus monkeys.

Journal: Science China. Life sciences

Published: July 25, 2025

Homozygous deleterious variants in MYCBPAP induce asthenoteratozoospermia involving abnormal acrosome biogenesis, manchette structure and sperm tail assembly in humans and mice.

Homozygous deleterious variants in MYCBPAP induce asthenoteratozoospermia involving abnormal acrosome biogenesis, manchette structure and sperm tail assembly in humans and mice.

Journal: Science China. Life sciences

Published: August 15, 2024

Deficiency of MFSD6L, an acrosome membrane protein, causes oligoasthenoteratozoospermia in humans and mice.

Deficiency of MFSD6L, an acrosome membrane protein, causes oligoasthenoteratozoospermia in humans and mice.

Journal: Journal of genetics and genomics = Yi chuan xue bao

Published: April 18, 2024

Dnali1 is required for sperm motility and male fertility in mice.

Dnali1 is required for sperm motility and male fertility in mice.

Journal: Basic and clinical andrology

Published: May 30, 2023

Deficiency of primate-specific SSX1 induced asthenoteratozoospermia in infertile men and cynomolgus monkey and tree shrew models.

Deficiency of primate-specific SSX1 induced asthenoteratozoospermia in infertile men and cynomolgus monkey and tree shrew models.

Journal: American journal of human genetics

Published: September 21, 2022

A homozygous frameshift mutation in ADAD2 causes male infertility with spermatogenic impairments.

A homozygous frameshift mutation in ADAD2 causes male infertility with spermatogenic impairments.

Journal: Journal of genetics and genomics = Yi chuan xue bao

Published: August 26, 2022

Biallelic mutations in CFAP54 cause male infertility with severe MMAF and NOA.

Biallelic mutations in CFAP54 cause male infertility with severe MMAF and NOA.

Journal: Journal of medical genetics

Published: August 23, 2022

Novel FSIP2 Variants Induce Super-Length Mitochondrial Sheath and Asthenoteratozoospermia in Humans.

Novel FSIP2 Variants Induce Super-Length Mitochondrial Sheath and Asthenoteratozoospermia in Humans.

Journal: International journal of biological sciences

Published: June 11, 2022

Homozygous variants in AKAP3 induce asthenoteratozoospermia and male infertility.

Homozygous variants in AKAP3 induce asthenoteratozoospermia and male infertility.

Journal: Journal of medical genetics

Published: October 17, 2021

Deficiency of X-linked TENT5D causes male infertility by disrupting the mRNA stability during spermatogenesis.

Deficiency of X-linked TENT5D causes male infertility by disrupting the mRNA stability during spermatogenesis.

Journal: Cell discovery

Published: October 10, 2021

Homozygous mutations in CCDC34 cause male infertility with oligoasthenoteratozoospermia in humans and mice.

Homozygous mutations in CCDC34 cause male infertility with oligoasthenoteratozoospermia in humans and mice.

Journal: Journal of medical genetics

Published: April 13, 2021

Showing 1-12 of 14

Last Updated: 09/26/2026