Cong Zhou

P.R. China
Chengdu, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 40 publications

A Novel CRYBB2 Splicing Mutation Is Associated With Lens Extracellular Matrix Remodeling and Vascular Alterations in Congenital Cataract.

A Novel CRYBB2 Splicing Mutation Is Associated With Lens Extracellular Matrix Remodeling and Vascular Alterations in Congenital Cataract.

Journal: Investigative ophthalmology & visual science

Published: April 16, 2026

Correction: Case Report: Novel mutations in two patients with MED13L-related intellectual disability highlighting the importance of genetic counseling.

Correction: Case Report: Novel mutations in two patients with MED13L-related intellectual disability highlighting the importance of genetic counseling.

Journal: Frontiers in genetics

Published: March 26, 2026

Semi-rigid linkers improve the pharmacokinetic properties and therapeutic efficacy of BET PROTACs for cancer therapy.

Semi-rigid linkers improve the pharmacokinetic properties and therapeutic efficacy of BET PROTACs for cancer therapy.

Journal: European journal of medicinal chemistry

Published: December 16, 2025

Single-cell transcriptomics identifies neural fate disruption and glial reprogramming caused by RARS2 deficiency.

Single-cell transcriptomics identifies neural fate disruption and glial reprogramming caused by RARS2 deficiency.

Journal: Journal of medical genetics

Published: December 01, 2025

Aberrant RNA splicing caused by variant in DEPDC5 identified in a patient with pharmacoresistant epilepsy.

Aberrant RNA splicing caused by variant in DEPDC5 identified in a patient with pharmacoresistant epilepsy.

Journal: Neurogenetics

Published: August 13, 2025

Case Report: Novel mutations in two patients with MED13L-related intellectual disability highlighting the importance of genetic counseling.

Case Report: Novel mutations in two patients with MED13L-related intellectual disability highlighting the importance of genetic counseling.

Journal: Frontiers in genetics

Published: July 20, 2025

Deciphering Glutaminyl Cyclase Catalytic Pathways Enables Recognition of Anchor Pharmacophores for Inhibitor Discovery.

Deciphering Glutaminyl Cyclase Catalytic Pathways Enables Recognition of Anchor Pharmacophores for Inhibitor Discovery.

Journal: Journal of chemical information and modeling

Published: May 14, 2025

Therapeutic Mechanism of Yihuo Huatan Formula in Stable Chronic Obstructive Pulmonary Disease: A Randomized Controlled Trial Integrating Metabolomics and 16S rRNA Gene Sequencing.

Therapeutic Mechanism of Yihuo Huatan Formula in Stable Chronic Obstructive Pulmonary Disease: A Randomized Controlled Trial Integrating Metabolomics and 16S rRNA Gene Sequencing.

Journal: Chinese journal of integrative medicine

Published: May 07, 2025

Spectrum and Frequencies of Genes for Inherited Hearing Loss in Southwestern Chinese Families.

Spectrum and Frequencies of Genes for Inherited Hearing Loss in Southwestern Chinese Families.

Journal: Genetic testing and molecular biomarkers

Published: April 29, 2025

Genetic diagnosis and prenatal diagnosis of patients with cystic kidney disease in Southwest China.

Genetic diagnosis and prenatal diagnosis of patients with cystic kidney disease in Southwest China.

Journal: BMC nephrology

Published: April 09, 2025

Novel MAP1B loss-of-function variant associated with periventricular nodular heterotopia 9 and literature review on genotype-phenotype associations of MAP1B.

Novel MAP1B loss-of-function variant associated with periventricular nodular heterotopia 9 and literature review on genotype-phenotype associations of MAP1B.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: April 03, 2025

Identification of a novel complex variant in a patient involving the α-globin gene cluster by third-generation sequencing.

Identification of a novel complex variant in a patient involving the α-globin gene cluster by third-generation sequencing.

Journal: Annals of hematology

Published: March 04, 2025

Showing 1-12 of 40

Last Updated: 09/26/2026