Tie Ke

Wuhan, 430074, China

Last Updated: 09/26/2026

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Found 27 publications

Functional characterization and allele-specific RNA interference-based rescue of KCNH2 p.F68C variant associated with long QT syndrome.

Functional characterization and allele-specific RNA interference-based rescue of KCNH2 p.F68C variant associated with long QT syndrome.

Journal: Molecular genetics and genomics : MGG

Published: November 02, 2025

The clinical effects of artificial dermis in the treatment of skin and soft tissue defects accompanied by bone or tendon exposure.

The clinical effects of artificial dermis in the treatment of skin and soft tissue defects accompanied by bone or tendon exposure.

Journal: Injury

Published: February 05, 2024

Aggf1 Specifies Hemangioblasts at the Top of Regulatory Hierarchy via Npas4l and mTOR-S6K-Emp2-ERK Signaling.

Aggf1 Specifies Hemangioblasts at the Top of Regulatory Hierarchy via Npas4l and mTOR-S6K-Emp2-ERK Signaling.

Journal: Arteriosclerosis, thrombosis, and vascular biology

Published: October 26, 2023

Genome-Wide Association Study for Idiopathic Ventricular Tachyarrhythmias Identifies Key Role of CCR7 and PKN2 in Calcium Homeostasis and Cardiac Rhythm Maintenance.

Genome-Wide Association Study for Idiopathic Ventricular Tachyarrhythmias Identifies Key Role of CCR7 and PKN2 in Calcium Homeostasis and Cardiac Rhythm Maintenance.

Journal: Circulation. Genomic and precision medicine

Published: July 27, 2022

NINJ2 deficiency inhibits preadipocyte differentiation and promotes insulin resistance through regulating insulin signaling.

NINJ2 deficiency inhibits preadipocyte differentiation and promotes insulin resistance through regulating insulin signaling.

Journal: Obesity (Silver Spring, Md.)

Published: April 26, 2022

Mog1 deficiency promotes cardiac contractile dysfunction and isoproterenol-induced arrhythmias associated with cardiac fibrosis and Cx43 remodeling.

Mog1 deficiency promotes cardiac contractile dysfunction and isoproterenol-induced arrhythmias associated with cardiac fibrosis and Cx43 remodeling.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: February 08, 2022

Identification and functional analysis of two new de novo KCNMA1 variants associated with Liang-Wang syndrome.

Identification and functional analysis of two new de novo KCNMA1 variants associated with Liang-Wang syndrome.

Journal: Acta physiologica (Oxford, England)

Published: January 01, 2022

KCNMA1 promotes obesity-related hypertension: Integrated analysis based on genome-wide association studies.

KCNMA1 promotes obesity-related hypertension: Integrated analysis based on genome-wide association studies.

Journal: Genes & diseases

Published: October 18, 2021

Mechanistic insights into the interaction of cardiac sodium channel Nav1.5 with MOG1 and a new molecular mechanism for Brugada syndrome.

Mechanistic insights into the interaction of cardiac sodium channel Nav1.5 with MOG1 and a new molecular mechanism for Brugada syndrome.

Journal: Heart rhythm

Published: March 25, 2021

A genome-wide association study identifies novel association between genetic variants in GGT7 and LINC00944 and hypertension.

A genome-wide association study identifies novel association between genetic variants in GGT7 and LINC00944 and hypertension.

Journal: Clinical and translational medicine

Published: December 03, 2020

Angiogenic factor AGGF1 acts as a tumor suppressor by modulating p53 post-transcriptional modifications and stability via MDM2.

Angiogenic factor AGGF1 acts as a tumor suppressor by modulating p53 post-transcriptional modifications and stability via MDM2.

Journal: Cancer letters

Published: August 16, 2020

Mog1 knockout causes cardiac hypertrophy and heart failure by downregulating tbx5-cryab-hspb2 signalling in zebrafish.

Mog1 knockout causes cardiac hypertrophy and heart failure by downregulating tbx5-cryab-hspb2 signalling in zebrafish.

Journal: Acta physiologica (Oxford, England)

Published: April 09, 2020

Showing 1-12 of 27

Last Updated: 09/26/2026