Jianteng Zhou

443 Huangshan Road
Hefei, 230027, China

Last Updated: 09/26/2026

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Found 31 publications

Loss-of-Function Variants in CCDC189 Cause Human Oligoasthenoteratozoospermia by Disrupting Sperm Flagellar and Acrosomal Architecture.

Loss-of-Function Variants in CCDC189 Cause Human Oligoasthenoteratozoospermia by Disrupting Sperm Flagellar and Acrosomal Architecture.

Journal: Andrology
Published: February 10, 2026

Podocyte mPGES-2 Determines Renal Aging and Contributes to Senile Osteoporosis.

Podocyte mPGES-2 Determines Renal Aging and Contributes to Senile Osteoporosis.

Journal: Aging cell
Published: November 06, 2025

Single-cell analysis of testicular bacterial microbiome changes during aging and effect on reproductive capacity in mice.

Single-cell analysis of testicular bacterial microbiome changes during aging and effect on reproductive capacity in mice.

Journal: iScience
Published: July 11, 2025

Genetic variation in gut microbe as a key regulator of host social behavior in C. elegans.

Genetic variation in gut microbe as a key regulator of host social behavior in C. elegans.

Journal: Gut microbes
Published: April 14, 2025

Deficiency in DNAH12 causes male infertility by impairing DNAH1 and DNALI1 recruitment in humans and mice.

Deficiency in DNAH12 causes male infertility by impairing DNAH1 and DNALI1 recruitment in humans and mice.

Journal: eLife
Published: March 27, 2025

Genetic and epigenetic mechanisms of GPRC5D loss after anti-GPRC5D CAR T-cell therapy in multiple myeloma.

Genetic and epigenetic mechanisms of GPRC5D loss after anti-GPRC5D CAR T-cell therapy in multiple myeloma.

Journal: Blood
Published: August 19, 2024

S100PBP interacts with nucleoporin TPR and facilitates XY crossover formation in mice.

S100PBP interacts with nucleoporin TPR and facilitates XY crossover formation in mice.

Journal: EMBO reports
Published: June 21, 2024

Pathogenic relationship between phenotypes of ARPKD and novel compound heterozygous mutations of PKHD1.

Pathogenic relationship between phenotypes of ARPKD and novel compound heterozygous mutations of PKHD1.

Journal: Frontiers in genetics
Published: May 08, 2024

A homozygous nonsense variant in HENMT1 causes male infertility in humans and mice.

A homozygous nonsense variant in HENMT1 causes male infertility in humans and mice.

Journal: Andrology
Published: April 26, 2024

CCDC157 is essential for sperm differentiation and shows oligoasthenoteratozoospermia-related mutations in men.

CCDC157 is essential for sperm differentiation and shows oligoasthenoteratozoospermia-related mutations in men.

Journal: Journal of cellular and molecular medicine
Published: October 30, 2023

A recessive ACTL7A founder variant leads to male infertility due to acrosome detachment in Pakistani Pashtuns.

A recessive ACTL7A founder variant leads to male infertility due to acrosome detachment in Pakistani Pashtuns.

Journal: Clinical genetics
Published: March 21, 2023

A novel recombination protein C12ORF40/REDIC1 is required for meiotic crossover formation.

A novel recombination protein C12ORF40/REDIC1 is required for meiotic crossover formation.

Journal: Cell discovery
Published: January 31, 2023
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Last Updated: 09/26/2026