Yingteng L. Zhang

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 15 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

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

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

Pulmonary amyloidosis in Sjögren's syndrome: a case report

Pulmonary amyloidosis in Sjögren's syndrome: a case report

Journal: Zhonghua jie he he hu xi za zhi = Zhonghua jiehe he huxi zazhi = Chinese journal of tuberculosis and respiratory diseases

Published: June 10, 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

DNAH3 deficiency causes flagellar inner dynein arm loss and male infertility in humans and mice.

DNAH3 deficiency causes flagellar inner dynein arm loss and male infertility in humans and mice.

Journal: eLife

Published: November 06, 2024

Identification of a Novel Biallelic CFAP119 Variant in an Infertile Man with Asthenoteratozoospermia.

Identification of a Novel Biallelic CFAP119 Variant in an Infertile Man with Asthenoteratozoospermia.

Journal: The world journal of men's health

Published: November 05, 2024

Establishing the causative link between CFAP221 variants and asthenoteratozoospermia in humans.

Establishing the causative link between CFAP221 variants and asthenoteratozoospermia in humans.

Journal: Journal of assisted reproduction and genetics

Published: October 26, 2024

Biallelic loss-of-function variants of DNAH7 cause male infertility associated with asthenozoospermia in humans.

Biallelic loss-of-function variants of DNAH7 cause male infertility associated with asthenozoospermia in humans.

Journal: Human genetics

Published: September 05, 2024

Showing 1-12 of 15

Last Updated: 09/26/2026