Mingwei Zhu

Guangzhou, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 21 publications

Microglial Inhibition Promotes Proliferation and Differentiation of Neural Stem Cells via STAT3/SDF-1/CXCR4 Signaling Pathway in Hypoxic-Ischemic Encephalopathy.

Microglial Inhibition Promotes Proliferation and Differentiation of Neural Stem Cells via STAT3/SDF-1/CXCR4 Signaling Pathway in Hypoxic-Ischemic Encephalopathy.

Journal: Glia

Published: August 08, 2025

Dysfunctional connectivity within hippocampal and entorhinal networks underlies early-life iron deficiency induced social recognition deficits, a preliminary study.

Dysfunctional connectivity within hippocampal and entorhinal networks underlies early-life iron deficiency induced social recognition deficits, a preliminary study.

Journal: Scientific reports

Published: June 06, 2025

MYH7, c.2011C>T, is responsible for congenital scoliosis in a Chinese family.

MYH7, c.2011C>T, is responsible for congenital scoliosis in a Chinese family.

Journal: Biochemistry and biophysics reports

Published: June 28, 2024

Radiographic features of congenital thumb duplication type C2 of Wu et al. classification: new subtypes and surgical strategies.

Radiographic features of congenital thumb duplication type C2 of Wu et al. classification: new subtypes and surgical strategies.

Journal: Frontiers in pediatrics

Published: August 31, 2023

A novel compound heterozygous variation in the FKBP10 gene causes Bruck syndrome without congenital contractures: A case report.

A novel compound heterozygous variation in the FKBP10 gene causes Bruck syndrome without congenital contractures: A case report.

Journal: Heliyon

Published: August 22, 2023

The mucolipidosis III-causing mutation in GNPTAB, c.1760G>C, disrupts the development of somites in rats.

The mucolipidosis III-causing mutation in GNPTAB, c.1760G>C, disrupts the development of somites in rats.

Journal: Genes & diseases

Published: July 21, 2023

Analysis of a case of Multiple pterygium syndrome due to a novel variant of CHRNG gene

Analysis of a case of Multiple pterygium syndrome due to a novel variant of CHRNG gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: May 22, 2023

Cataract-causing Y204X mutation of crystallin protein CRYβB1 promotes its C-terminal degradation and higher-order oligomerization.

Cataract-causing Y204X mutation of crystallin protein CRYβB1 promotes its C-terminal degradation and higher-order oligomerization.

Journal: The Journal of biological chemistry

Published: May 11, 2023

A novel mutation in intron 1 of Wnt1 causes developmental loss of dopaminergic neurons in midbrain and ASD-like behaviors in rats.

A novel mutation in intron 1 of Wnt1 causes developmental loss of dopaminergic neurons in midbrain and ASD-like behaviors in rats.

Journal: Molecular psychiatry

Published: February 01, 2023

Novel denovo TRPV4 mutation identified in a Chinese family with metatropic dysplasia inhibits chondrogenic differentiation.

Novel denovo TRPV4 mutation identified in a Chinese family with metatropic dysplasia inhibits chondrogenic differentiation.

Journal: Genes & diseases

Published: January 11, 2023

Epidemiological characteristics and distribution of congenital thumb duplication in south China: An analysis of 2,300 thumbs in 2,108 children.

Epidemiological characteristics and distribution of congenital thumb duplication in south China: An analysis of 2,300 thumbs in 2,108 children.

Journal: Frontiers in pediatrics

Published: August 24, 2022

Selective targeting of MD2 attenuates intestinal inflammation and prevents neonatal necrotizing enterocolitis by suppressing TLR4 signaling.

Selective targeting of MD2 attenuates intestinal inflammation and prevents neonatal necrotizing enterocolitis by suppressing TLR4 signaling.

Journal: Frontiers in immunology

Published: August 02, 2022

Showing 1-12 of 21

Last Updated: 09/26/2026