Ying O. Shen

Key Laboratory Of Birth Defects And Related Disease Of Women And Children Of Ministry Of Education
Chengdu, 610041, China

Last Updated: 09/26/2026

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Found 85 publications

ASB9 promotes ubiquitin-mediated degradation of TNP2 to facilitate histone-to-protamine transition in humans and mice.

ASB9 promotes ubiquitin-mediated degradation of TNP2 to facilitate histone-to-protamine transition in humans and mice.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: March 31, 2026

Novel NUP210L Variants Cause Fertilization Failure and Male Infertility in Humans.

Novel NUP210L Variants Cause Fertilization Failure and Male Infertility in Humans.

Journal: Clinical genetics

Published: March 24, 2026

Biallelic Variants in ATP1A4 Are Associated with Oligoasthenoteratozoospermia and Male Infertility.

Biallelic Variants in ATP1A4 Are Associated with Oligoasthenoteratozoospermia and Male Infertility.

Journal: Clinical genetics

Published: March 17, 2026

Sequencing the CCDC146 gene in a large cohort of infertile Chinese men reveals novel mutations in patients with asthenoteratozoospermia.

Sequencing the CCDC146 gene in a large cohort of infertile Chinese men reveals novel mutations in patients with asthenoteratozoospermia.

Journal: Chinese medical journal

Published: November 15, 2025

DNAH14 deficiency disrupts sperm annulus positioning and compromises offspring postnatal development.

DNAH14 deficiency disrupts sperm annulus positioning and compromises offspring postnatal development.

Journal: Human reproduction (Oxford, England)

Published: October 13, 2025

A novel dual histone mark reader ZCWPW2 regulates meiotic recombination through lactylation and transcriptional regulation in humans and mice.

A novel dual histone mark reader ZCWPW2 regulates meiotic recombination through lactylation and transcriptional regulation in humans and mice.

Journal: Nucleic acids research

Published: July 15, 2025

Furin-Mediated Cleavage of Zona Pellucida Proteins Is Essential for Oocyte Development.

Furin-Mediated Cleavage of Zona Pellucida Proteins Is Essential for Oocyte Development.

Journal: MedComm

Published: July 10, 2025

Discovery of a Pathogenic NME5 Variant Underlying Acephalic Spermatozoa Syndrome: Unraveling a Novel Genotype-Phenotype Association in Male Infertility.

Discovery of a Pathogenic NME5 Variant Underlying Acephalic Spermatozoa Syndrome: Unraveling a Novel Genotype-Phenotype Association in Male Infertility.

Journal: Clinical genetics

Published: July 01, 2025

Loss of Different Domains of TDRD12 Leads to Distinct Male Infertility-Related Phenotypes.

Loss of Different Domains of TDRD12 Leads to Distinct Male Infertility-Related Phenotypes.

Journal: Clinical genetics

Published: May 21, 2025

Whole Exome Sequencing Identified Novel Pathogenic Mutations of ADGB in Patients With Oligoasthenozoospermia

Whole Exome Sequencing Identified Novel Pathogenic Mutations of ADGB in Patients With Oligoasthenozoospermia

Journal: Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition

Published: May 10, 2025

Cholesterol Sulfate: Pathophysiological Implications and Potential Therapeutics.

Cholesterol Sulfate: Pathophysiological Implications and Potential Therapeutics.

Journal: Biomolecules

Published: March 10, 2025

Investigating the role of a testis-expressed gene Tex2 in spermatogenesis in mice.

Investigating the role of a testis-expressed gene Tex2 in spermatogenesis in mice.

Journal: Molecular human reproduction

Published: January 11, 2025

Showing 1-12 of 85

Last Updated: 09/26/2026