Yu-xing Liu

Changsha, 410028, China

Last Updated: 09/26/2026

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Found 15 publications

Lipin3 deficiency promotes hepatocyte ferroptosis and pyroptosis via activating JAK1-STAT3 pathway during acetaminophen induced acute liver injury.

Lipin3 deficiency promotes hepatocyte ferroptosis and pyroptosis via activating JAK1-STAT3 pathway during acetaminophen induced acute liver injury.

Journal: Molecular biomedicine
Published: March 03, 2025

Lipin3 deficiency aggravates cisplatin induced acute kidney injury via activating Sirt1-p21-Caspase 3-GSDME pyroptosis pathway.

Lipin3 deficiency aggravates cisplatin induced acute kidney injury via activating Sirt1-p21-Caspase 3-GSDME pyroptosis pathway.

Journal: International journal of biological sciences
Published: January 08, 2025

Novel heterozygous mutation of CACNA2D1 gene in a Chinese family with arrhythmia.

Novel heterozygous mutation of CACNA2D1 gene in a Chinese family with arrhythmia.

Journal: BMC cardiovascular disorders
Published: May 22, 2024

Single-cell transcriptomic profiling reveals decreased ER protein Reticulon3 drives the progression of renal fibrosis.

Single-cell transcriptomic profiling reveals decreased ER protein Reticulon3 drives the progression of renal fibrosis.

Journal: Molecular biomedicine
Published: March 13, 2024

RTN3 deficiency exacerbates cisplatin-induced acute kidney injury through the disruption of mitochondrial stability.

RTN3 deficiency exacerbates cisplatin-induced acute kidney injury through the disruption of mitochondrial stability.

Journal: Mitochondrion
Published: September 04, 2023

Case report: A novel WASHC5 variant altering mRNA splicing causes spastic paraplegia in a patient.

Case report: A novel WASHC5 variant altering mRNA splicing causes spastic paraplegia in a patient.

Journal: Frontiers in genetics
Published: May 04, 2023

Case report: A novel mutation of RecQ-like helicase 5 in a Chinese family with early myocardial infarction, coronary artery disease, and stroke hemiplegia.

Case report: A novel mutation of RecQ-like helicase 5 in a Chinese family with early myocardial infarction, coronary artery disease, and stroke hemiplegia.

Journal: Frontiers in genetics
Published: January 18, 2023

The first case report of CODAS syndrome in Chinese population caused by two LONP1 pathogenic mutations.

The first case report of CODAS syndrome in Chinese population caused by two LONP1 pathogenic mutations.

Journal: Frontiers in genetics
Published: August 30, 2022

Doubly bi-allelic variants of MTHFR and MTHFD1 in a Chinese patient with hyperhomocysteinemia and failure of folic acid therapy.

Doubly bi-allelic variants of MTHFR and MTHFD1 in a Chinese patient with hyperhomocysteinemia and failure of folic acid therapy.

Journal: Frontiers in genetics
Published: July 11, 2022

Case report: Whole-exome sequencing identifies a novel DES mutation (p. E434K) in a Chinese family with cardiomyopathy and sudden cardiac death.

Case report: Whole-exome sequencing identifies a novel DES mutation (p. E434K) in a Chinese family with cardiomyopathy and sudden cardiac death.

Journal: Frontiers in cardiovascular medicine
Published: June 17, 2022

A Novel Homozygous Variant of TMEM231 in a Case With Hypoplasia of the Cerebellar Vermis and Polydactyly.

A Novel Homozygous Variant of TMEM231 in a Case With Hypoplasia of the Cerebellar Vermis and Polydactyly.

Journal: Frontiers in pediatrics
Published: September 12, 2021

Case Report: A Novel Heterozygous Mutation of CD2AP in a Chinese Family With Proteinuria Leads to Focal Segmental Glomerulosclerosis.

Case Report: A Novel Heterozygous Mutation of CD2AP in a Chinese Family With Proteinuria Leads to Focal Segmental Glomerulosclerosis.

Journal: Frontiers in pediatrics
Published: March 29, 2021
Showing 1-12 of 15

Last Updated: 09/26/2026