Qing Ke

WNT5a-Mediated Aberrant Actin Filament Dynamics Drive Cardiac Pathogenic Phenotypes in LMNA-Related Emery-Dreifuss Muscular Dystrophy.

Journal: Circulation

Published: April 17, 2026

Current status of interventional therapy for hepatic encephalopathy associated with spontaneous portosystemic shunts

Journal: Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology

Published: July 15, 2025

iPSC-derived cardiomyocytes and engineered heart tissues reveal suppressed JAK2/STAT3 signaling in LMNA-related emery-dreifuss muscular dystrophy.

Journal: Redox biology

Published: March 06, 2025

Clinical and Genetic Findings in a Chinese Cohort of Dentatorubral-Pallidoluysian Atrophy Patients.

Journal: Annals of neurology

Published: January 07, 2025

A novel 8-octapeptide repeat insertion in PRNP causing Huntington disease-like 1 in a Chinese family: a case report and literature review.

Journal: Journal of medical genetics

Published: November 18, 2024

Reply to Vaccario et al.: The role of baselines in fair and unbiased citation metric evaluation.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: September 30, 2024

METTL14 Promotes the Osteogenic Differentiation of Human Bone Marrow Stromal Cells via m6A-Dependent Stabilization of USP7 mRNA.

Journal: Biochemical genetics

Published: September 18, 2024

Familial hypercholesterolemia in Chinese children and adolescents: a multicenter study.

Journal: Lipids in health and disease

Published: August 26, 2024

Constructing a cataplexy face prediction model for narcolepsy type 1 based on ResNet-18

Journal: Zhonghua yi xue za zhi

Published: July 09, 2024

High-risk screening for late-onset Pompe disease in China: An expanded multicenter study.

Journal: Journal of inherited metabolic disease

Published: June 12, 2024

WNT5a-Mediated Aberrant Actin Filament Dynamics Drive Cardiac Pathogenic Phenotypes in LMNA-Related Emery-Dreifuss Muscular Dystrophy.

WNT5a-Mediated Aberrant Actin Filament Dynamics Drive Cardiac Pathogenic Phenotypes in LMNA-Related Emery-Dreifuss Muscular Dystrophy.

Current status of interventional therapy for hepatic encephalopathy associated with spontaneous portosystemic shunts

Current status of interventional therapy for hepatic encephalopathy associated with spontaneous portosystemic shunts

iPSC-derived cardiomyocytes and engineered heart tissues reveal suppressed JAK2/STAT3 signaling in LMNA-related emery-dreifuss muscular dystrophy.

iPSC-derived cardiomyocytes and engineered heart tissues reveal suppressed JAK2/STAT3 signaling in LMNA-related emery-dreifuss muscular dystrophy.

Clinical and Genetic Findings in a Chinese Cohort of Dentatorubral-Pallidoluysian Atrophy Patients.

Clinical and Genetic Findings in a Chinese Cohort of Dentatorubral-Pallidoluysian Atrophy Patients.

A novel 8-octapeptide repeat insertion in PRNP causing Huntington disease-like 1 in a Chinese family: a case report and literature review.

A novel 8-octapeptide repeat insertion in PRNP causing Huntington disease-like 1 in a Chinese family: a case report and literature review.

Reply to Vaccario et al.: The role of baselines in fair and unbiased citation metric evaluation.

Reply to Vaccario et al.: The role of baselines in fair and unbiased citation metric evaluation.

METTL14 Promotes the Osteogenic Differentiation of Human Bone Marrow Stromal Cells via m6A-Dependent Stabilization of USP7 mRNA.

METTL14 Promotes the Osteogenic Differentiation of Human Bone Marrow Stromal Cells via m6A-Dependent Stabilization of USP7 mRNA.

Familial hypercholesterolemia in Chinese children and adolescents: a multicenter study.

Familial hypercholesterolemia in Chinese children and adolescents: a multicenter study.

Constructing a cataplexy face prediction model for narcolepsy type 1 based on ResNet-18

Constructing a cataplexy face prediction model for narcolepsy type 1 based on ResNet-18

High-risk screening for late-onset Pompe disease in China: An expanded multicenter study.

High-risk screening for late-onset Pompe disease in China: An expanded multicenter study.

Novel variants and genotype-phenotype correlation in a multicentre cohort of GNE myopathy in China.

Novel variants and genotype-phenotype correlation in a multicentre cohort of GNE myopathy in China.

Dentatorubral-pallidoluysian atrophy: a case report and review of literature.

Dentatorubral-pallidoluysian atrophy: a case report and review of literature.