Congjing Wang

State Key Laboratory Of Reproductive Medicine And Offspring Health
Nanjing, China

Last Updated: 09/26/2026

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Found 11 publications

Farnesylation-dependent kinetochore targeting of centromere protein F is essential for oocyte meiotic progression and female fertility.

Farnesylation-dependent kinetochore targeting of centromere protein F is essential for oocyte meiotic progression and female fertility.

Journal: American journal of obstetrics and gynecology

Published: May 27, 2025

The role of SRPK1-mediated phosphorylation of SR proteins in the chromatin configuration transition of mouse germinal vesicle oocytes.

The role of SRPK1-mediated phosphorylation of SR proteins in the chromatin configuration transition of mouse germinal vesicle oocytes.

Journal: Journal of biomedical research

Published: May 29, 2024

Variants in NLRP2 and ZFP36L2, non-core components of the human subcortical maternal complex, cause female infertility with embryonic development arrest.

Variants in NLRP2 and ZFP36L2, non-core components of the human subcortical maternal complex, cause female infertility with embryonic development arrest.

Journal: Molecular human reproduction

Published: January 08, 2024

Mutations in CCNB3 affect its location thus causing a multiplicity of phenotypes in human oocytes maturation by aberrant CDK1 activity and APC/C activity at different stages.

Mutations in CCNB3 affect its location thus causing a multiplicity of phenotypes in human oocytes maturation by aberrant CDK1 activity and APC/C activity at different stages.

Journal: Journal of ovarian research

Published: February 27, 2023

NLRP7 participates in the human subcortical maternal complex and its variants cause female infertility characterized by early embryo arrest.

NLRP7 participates in the human subcortical maternal complex and its variants cause female infertility characterized by early embryo arrest.

Journal: Journal of molecular medicine (Berlin, Germany)

Published: October 12, 2022

Correction to: Expanding the Genetic and Phenotypic Spectrum of Female Infertility Caused by TUBB8 Mutations.

Correction to: Expanding the Genetic and Phenotypic Spectrum of Female Infertility Caused by TUBB8 Mutations.

Journal: Reproductive sciences (Thousand Oaks, Calif.)

Published: September 20, 2021

Integrative proteome analysis implicates aberrant RNA splicing in impaired developmental potential of aged mouse oocytes.

Integrative proteome analysis implicates aberrant RNA splicing in impaired developmental potential of aged mouse oocytes.

Journal: Aging cell

Published: March 11, 2021

Expanding the Genetic and Phenotypic Spectrum of Female Infertility Caused by TUBB8 Mutations.

Expanding the Genetic and Phenotypic Spectrum of Female Infertility Caused by TUBB8 Mutations.

Journal: Reproductive sciences (Thousand Oaks, Calif.)

Published: February 02, 2021

Maternal RNF114-mediated target substrate degradation regulates zygotic genome activation in mouse embryos.

Maternal RNF114-mediated target substrate degradation regulates zygotic genome activation in mouse embryos.

Journal: Development (Cambridge, England)

Published: January 17, 2021

The Recurrent Mutation in PATL2 Inhibits Its Degradation Thus Causing Female Infertility Characterized by Oocyte Maturation Defect Through Regulation of the Mos-MAPK Pathway.

The Recurrent Mutation in PATL2 Inhibits Its Degradation Thus Causing Female Infertility Characterized by Oocyte Maturation Defect Through Regulation of the Mos-MAPK Pathway.

Journal: Frontiers in cell and developmental biology

Published: November 12, 2020

Heterozygous mutations in ZP1 and ZP3 cause formation disorder of ZP and female infertility in human.

Heterozygous mutations in ZP1 and ZP3 cause formation disorder of ZP and female infertility in human.

Journal: Journal of cellular and molecular medicine

Published: February 11, 2020

Showing 1-11 of 11

Last Updated: 09/26/2026