Zhuo X. Meng

No. 1665, Kongjiang Road
Yangpu, 200092, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 16 publications

Corrigendum to 'Cuproptosis in osteoarthritis: Exploring chondrocyte cuproptosis and therapeutic avenues' [J Orthop Translat (2025) 292-308/JOT 1002].

Corrigendum to 'Cuproptosis in osteoarthritis: Exploring chondrocyte cuproptosis and therapeutic avenues' [J Orthop Translat (2025) 292-308/JOT 1002].

Journal: Journal of orthopaedic translation

Published: May 01, 2026

Analysis of gene expression in synovial fluid and blood of patients with knee osteoarthritis of Yang deficiency and blood stasis type

Analysis of gene expression in synovial fluid and blood of patients with knee osteoarthritis of Yang deficiency and blood stasis type

Journal: Zhongguo gu shang = China journal of orthopaedics and traumatology

Published: September 03, 2025

Cuproptosis in osteoarthritis: Exploring chondrocyte cuproptosis and therapeutic avenues.

Cuproptosis in osteoarthritis: Exploring chondrocyte cuproptosis and therapeutic avenues.

Journal: Journal of orthopaedic translation

Published: May 23, 2025

ELABELA Targets Mitochondria to Modulate Heart Development.

ELABELA Targets Mitochondria to Modulate Heart Development.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Published: April 14, 2025

ELABELA-32 Alleviates Doxorubicin-Induced Chronic Cardiotoxicity by Inhibiting the TGF-β/Smad Signaling Pathway.

ELABELA-32 Alleviates Doxorubicin-Induced Chronic Cardiotoxicity by Inhibiting the TGF-β/Smad Signaling Pathway.

Journal: Cardiovascular toxicology

Published: November 04, 2024

Manic Fringe promotes endothelial-to-mesenchymal transition mediated by the Notch signalling pathway during heart valve development.

Manic Fringe promotes endothelial-to-mesenchymal transition mediated by the Notch signalling pathway during heart valve development.

Journal: Journal of molecular medicine (Berlin, Germany)

Published: November 30, 2023

Identification of Rare Variants in Right Ventricular Outflow Tract Obstruction Congenital Heart Disease by Whole-Exome Sequencing.

Identification of Rare Variants in Right Ventricular Outflow Tract Obstruction Congenital Heart Disease by Whole-Exome Sequencing.

Journal: Frontiers in cardiovascular medicine

Published: November 08, 2021

A loss-of-function mutation p.T256M in NDRG4 is implicated in the pathogenesis of pulmonary atresia with ventricular septal defect (PA/VSD) and tetralogy of Fallot (TOF).

A loss-of-function mutation p.T256M in NDRG4 is implicated in the pathogenesis of pulmonary atresia with ventricular septal defect (PA/VSD) and tetralogy of Fallot (TOF).

Journal: FEBS open bio

Published: September 03, 2020

Dynamic transcriptome profiling toward understanding the development of the human embryonic heart during different Carnegie stages.

Dynamic transcriptome profiling toward understanding the development of the human embryonic heart during different Carnegie stages.

Journal: FEBS letters

Published: April 22, 2020

Mutations in fibroblast growth factor (FGF8) and FGF10 identified in patients with conotruncal defects.

Mutations in fibroblast growth factor (FGF8) and FGF10 identified in patients with conotruncal defects.

Journal: Journal of translational medicine

Published: March 04, 2020

Essential Role of the ELABELA-APJ Signaling Pathway in Cardiovascular System Development and Diseases.

Essential Role of the ELABELA-APJ Signaling Pathway in Cardiovascular System Development and Diseases.

Journal: Journal of cardiovascular pharmacology

Published: January 31, 2020

Rab5a activates IRS1 to coordinate IGF-AKT-mTOR signaling and myoblast differentiation during muscle regeneration.

Rab5a activates IRS1 to coordinate IGF-AKT-mTOR signaling and myoblast differentiation during muscle regeneration.

Journal: Cell death and differentiation

Published: June 25, 2019

Showing 1-12 of 16

Last Updated: 09/26/2026