Gan 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

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 18 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

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

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

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

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

Identification of an SMC1B Mutation Associated With Necrozoospermia and Failure of Testi-ICSI : SMC1B Mutation Associated With Necrozoospermia.

Identification of an SMC1B Mutation Associated With Necrozoospermia and Failure of Testi-ICSI : SMC1B Mutation Associated With Necrozoospermia.

Journal: Reproductive sciences (Thousand Oaks, Calif.)

Published: November 17, 2024

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

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 18

Last Updated: 09/26/2026