Yunchuan Tian

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 10 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

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

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

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

Roles of lipid metabolism and its regulatory mechanism in idiopathic pulmonary fibrosis: A review.

Roles of lipid metabolism and its regulatory mechanism in idiopathic pulmonary fibrosis: A review.

Journal: The international journal of biochemistry & cell biology

Published: August 22, 2022

Showing 1-10 of 10

Last Updated: 09/26/2026