Jiayi Pei

Utrecht, UT, Netherlands

Last Updated: 09/26/2026

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Found 20 publications

Targeting lipid metabolism as a new therapeutic strategy for inherited cardiomyopathies.

Targeting lipid metabolism as a new therapeutic strategy for inherited cardiomyopathies.

Journal: Frontiers in cardiovascular medicine

Published: December 02, 2022

Chromatin Immunoprecipitation Sequencing (ChIP-seq) Protocol for Small Amounts of Frozen Biobanked Cardiac Tissue.

Chromatin Immunoprecipitation Sequencing (ChIP-seq) Protocol for Small Amounts of Frozen Biobanked Cardiac Tissue.

Journal: Methods in molecular biology (Clifton, N.J.)

Published: February 01, 2022

Sarcomere Disassembly and Transfection Efficiency in Proliferating Human iPSC-Derived Cardiomyocytes.

Sarcomere Disassembly and Transfection Efficiency in Proliferating Human iPSC-Derived Cardiomyocytes.

Journal: Journal of cardiovascular development and disease

Published: September 30, 2021

Unfolded Protein Response as a Compensatory Mechanism and Potential Therapeutic Target in PLN R14del Cardiomyopathy.

Unfolded Protein Response as a Compensatory Mechanism and Potential Therapeutic Target in PLN R14del Cardiomyopathy.

Journal: Circulation

Published: April 30, 2021

Metabolomics in Severe Aortic Stenosis Reveals Intermediates of Nitric Oxide Synthesis as Most Distinctive Markers.

Metabolomics in Severe Aortic Stenosis Reveals Intermediates of Nitric Oxide Synthesis as Most Distinctive Markers.

Journal: International journal of molecular sciences

Published: March 21, 2021

Proteomic and Functional Studies Reveal Detyrosinated Tubulin as Treatment Target in Sarcomere Mutation-Induced Hypertrophic Cardiomyopathy.

Proteomic and Functional Studies Reveal Detyrosinated Tubulin as Treatment Target in Sarcomere Mutation-Induced Hypertrophic Cardiomyopathy.

Journal: Circulation. Heart failure

Published: January 12, 2021

Multi-omics integration identifies key upstream regulators of pathomechanisms in hypertrophic cardiomyopathy due to truncating MYBPC3 mutations.

Multi-omics integration identifies key upstream regulators of pathomechanisms in hypertrophic cardiomyopathy due to truncating MYBPC3 mutations.

Journal: Clinical epigenetics

Published: September 30, 2020

Strength of patient cohorts and biobanks for cardiomyopathy research.

Strength of patient cohorts and biobanks for cardiomyopathy research.

Journal: Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation

Published: August 12, 2020

Statistical integration of two omics datasets using GO2PLS.

Statistical integration of two omics datasets using GO2PLS.

Journal: BMC bioinformatics

Published: July 29, 2020

A new microfluidic model that allows monitoring of complex vascular structures and cell interactions in a 3D biological matrix.

A new microfluidic model that allows monitoring of complex vascular structures and cell interactions in a 3D biological matrix.

Journal: Lab on a chip

Published: April 25, 2020

Mutation location of HCM-causing troponin T mutations defines the degree of myofilament dysfunction in human cardiomyocytes.

Mutation location of HCM-causing troponin T mutations defines the degree of myofilament dysfunction in human cardiomyocytes.

Journal: Journal of molecular and cellular cardiology

Published: April 23, 2020

H3K27ac acetylome signatures reveal the epigenomic reorganization in remodeled non-failing human hearts.

H3K27ac acetylome signatures reveal the epigenomic reorganization in remodeled non-failing human hearts.

Journal: Clinical epigenetics

Published: April 06, 2020

Showing 1-12 of 20

Last Updated: 09/26/2026