Mingrui Lin
Fuzhou, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 13 publications
Genotype and phenotype correlation analysis in 27 families with multiple osteochondroma and validation by ATDC5 chondrocyte models.
Journal: Bone & joint research
Published: October 27, 2025
Mavacamten alleviates sepsis-induced acute respiratory distress syndrome by modulating the PI3K/AKT/autophagy axis: a spatial transcriptomic-guided investigation.
Journal: Journal of translational medicine
Published: September 18, 2025
LncRNA-TUG1: Implications in the Myocardial and Endothelial Cell Oxidative Stress Injury Caused by Hemorrhagic Shock and Fluid Resuscitation.
Journal: Frontiers in bioscience (Landmark edition)
Published: July 02, 2024
One-pot hydrothermal synthesis of silicon, nitrogen co-doped carbon dots for enhancing enzyme activity of acid phosphatase (ACP) to dopamine and for cell imaging.
Journal: Talanta
Published: February 02, 2024
Xijiao Dihuang Decoction Protects Against Murine Sepsis-Induced Cardiac Inflammation and Apoptosis via Suppressing TLR4/NF-κB and Activating PI3K/AKT Pathway.
Journal: Journal of inflammation research
Published: October 19, 2023
Two Novel Frameshift Mutations in the GLI3 Gene Underlie Non-Syndromic Polydactyly in Chinese Families.
Journal: Genetic testing and molecular biomarkers
Published: September 28, 2023
A Novel Intronic Splicing Mutation in the EXT2 Gene of a Chinese Family with Multiple Osteochondroma.
Journal: Genetic testing and molecular biomarkers
Published: July 19, 2021
Analysis of genetic variants in a pedigree affected with hereditary multiple osteochondroma
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: June 07, 2021
A Nonsense Mutation in HOXD13 Gene from A Chinese Family with Non-Syndromic Synpolydactyly.
Journal: The Tohoku journal of experimental medicine
Published: October 16, 2019
A novel splice mutation induces exon skipping of the EXT1 gene in patients with hereditary multiple exostoses.
Journal: International journal of oncology
Published: July 03, 2018
Targeted Next-Generation Sequencing Newly Identifies Mutations in Exostosin-1 and Exostosin-2 Genes of Patients with Multiple Osteochondromas.
Journal: The Tohoku journal of experimental medicine
Published: July 11, 2017
Last Updated: 09/26/2026