Chengyue F. Sun

Beijing, China

Last Updated: 09/26/2026

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Found 23 publications

Pathogenic mechanisms in Fabry disease.

Pathogenic mechanisms in Fabry disease.

Journal: Frontiers in medicine

Published: April 28, 2026

Clinical analysis of pediatric restrictive cardiomyopathy associated with FLNC gene variants in 5 children

Clinical analysis of pediatric restrictive cardiomyopathy associated with FLNC gene variants in 5 children

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics

Published: April 15, 2026

Artificial cells with liquid-liquid phase separation-regulated cell-free protein synthesis.

Artificial cells with liquid-liquid phase separation-regulated cell-free protein synthesis.

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

Published: November 21, 2025

A Weibull distribution-based method for estimating seed longevity in Solanum rostratum.

A Weibull distribution-based method for estimating seed longevity in Solanum rostratum.

Journal: Frontiers in plant science

Published: September 07, 2025

Single-Nucleus RNA Sequencing Unravels Early Mechanisms of Human Becker Muscular Dystrophy.

Single-Nucleus RNA Sequencing Unravels Early Mechanisms of Human Becker Muscular Dystrophy.

Journal: Annals of neurology

Published: March 12, 2024

A novel deep intronic variant introduce dystrophin pseudoexon in Becker muscular dystrophy: A case report.

A novel deep intronic variant introduce dystrophin pseudoexon in Becker muscular dystrophy: A case report.

Journal: Heliyon

Published: August 29, 2023

Comparing adverse events of tenecteplase and alteplase: a real-world analysis of the FDA adverse event reporting system (FAERS).

Comparing adverse events of tenecteplase and alteplase: a real-world analysis of the FDA adverse event reporting system (FAERS).

Journal: Expert opinion on drug safety

Published: August 09, 2023

A new pseudoexon activation due to ultrarare branch point formation in Duchenne muscular dystrophy.

A new pseudoexon activation due to ultrarare branch point formation in Duchenne muscular dystrophy.

Journal: Neuromuscular disorders : NMD

Published: July 20, 2023

Cryptic exon activation caused by a novel deep-intronic splice-altering variant in Becker muscular dystrophy.

Cryptic exon activation caused by a novel deep-intronic splice-altering variant in Becker muscular dystrophy.

Journal: Journal of clinical laboratory analysis

Published: July 12, 2023

A novel biomarker of fibrofatty replacement in dystrophinopathies identified by integrating transcriptome, magnetic resonance imaging, and pathology data.

A novel biomarker of fibrofatty replacement in dystrophinopathies identified by integrating transcriptome, magnetic resonance imaging, and pathology data.

Journal: Journal of cachexia, sarcopenia and muscle

Published: April 19, 2023

Clinical and genetic interpretation of uncertain DMD missense variants: evidence from mRNA and protein studies.

Clinical and genetic interpretation of uncertain DMD missense variants: evidence from mRNA and protein studies.

Journal: Orphanet journal of rare diseases

Published: April 17, 2023

A 10-year retrospective analysis of spectrums and treatment options of orthostatic intolerance and sitting intolerance in children

A 10-year retrospective analysis of spectrums and treatment options of orthostatic intolerance and sitting intolerance in children

Journal: Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences

Published: October 14, 2022

Showing 1-12 of 23

Last Updated: 09/26/2026