Yingying Yin

Key Laboratory Of Experimental Teratology
Jinan, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 14 publications

TMC7 deficiency causes acrosome biogenesis defects and male infertility in mice.

TMC7 deficiency causes acrosome biogenesis defects and male infertility in mice.

Journal: eLife

Published: September 13, 2024

TTC6-Mediated Stabilization of the Flagellum Annulus Ensures the Rapid and Directed Motion of Sperm.

TTC6-Mediated Stabilization of the Flagellum Annulus Ensures the Rapid and Directed Motion of Sperm.

Journal: Cells

Published: July 18, 2023

CCDC178-mediated cytoskeleton assembly is required for spermiogenesis in mice.

CCDC178-mediated cytoskeleton assembly is required for spermiogenesis in mice.

Journal: Genes & diseases

Published: July 13, 2023

Deficiency of the Tmem232 Gene Causes Male Infertility with Morphological Abnormalities of the Sperm Flagellum in Mice.

Deficiency of the Tmem232 Gene Causes Male Infertility with Morphological Abnormalities of the Sperm Flagellum in Mice.

Journal: Cells

Published: April 24, 2023

CCDC176 stabilizes microtubule doublets 1 and 9 to ensure proper sperm movement.

CCDC176 stabilizes microtubule doublets 1 and 9 to ensure proper sperm movement.

Journal: Current biology : CB

Published: February 22, 2023

LRRC46 Accumulates at the Midpiece of Sperm Flagella and Is Essential for Spermiogenesis and Male Fertility in Mouse.

LRRC46 Accumulates at the Midpiece of Sperm Flagella and Is Essential for Spermiogenesis and Male Fertility in Mouse.

Journal: International journal of molecular sciences

Published: June 27, 2022

IGF2 improves the developmental competency and meiotic structure of oocytes from aged mice.

IGF2 improves the developmental competency and meiotic structure of oocytes from aged mice.

Journal: Aging

Published: June 26, 2020

The histone modification reader ZCWPW1 links histone methylation to PRDM9-induced double-strand break repair.

The histone modification reader ZCWPW1 links histone methylation to PRDM9-induced double-strand break repair.

Journal: eLife

Published: November 08, 2019

Absence of murine CFAP61 causes male infertility due to multiple morphological abnormalities of the flagella.

Absence of murine CFAP61 causes male infertility due to multiple morphological abnormalities of the flagella.

Journal: Science bulletin

Published: August 21, 2019

SCRE serves as a unique synaptonemal complex fastener and is essential for progression of meiosis prophase I in mice.

SCRE serves as a unique synaptonemal complex fastener and is essential for progression of meiosis prophase I in mice.

Journal: Nucleic acids research

Published: January 20, 2019

Association study between IL-1β-511 C/T polymorphism and obsessive-compulsive disorder (OCD) in Chinese Han population.

Association study between IL-1β-511 C/T polymorphism and obsessive-compulsive disorder (OCD) in Chinese Han population.

Journal: International journal of psychiatry in medicine

Published: February 21, 2014

A case-control study of interleukin-12 1188A/C polymorphism in obsessive-compulsive disorder in Chinese population.

A case-control study of interleukin-12 1188A/C polymorphism in obsessive-compulsive disorder in Chinese population.

Journal: Acta neuropsychiatrica

Published: June 01, 2012

Showing 1-12 of 14

Last Updated: 09/26/2026