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Publications by Dina Myers Stroud

Striking in Vivo Phenotype of a Disease-Associated Human SCN5A Mutation Producing Minimal Changes in Vitro

Cardiovascular Medicine

English

Informatic and Functional Approaches to Identifying a Regulatory Region for the Cardiac Sodium Channel

Circulation Research

Cardiovascular Medicine

English

Related publications

Genetic Variants in SCN5A Promoter Are Associated With Arrhythmia Phenotype Severity in Patients With Heterozygous Loss-Of-Function Mutation

Cardiovascular Medicine

English

SCN5A Mutation Associated With Acute Myocardial Infarction

Forensic Medicine

English

Genotype-Phenotype Relationship and Risk Stratification in Loss-Of-Function SCN5A Mutation Carriers

Annals of Noninvasive Electrocardiology

Cardiovascular Medicine

English

Whole‑exome Sequencing Identifies a Novel Mutation (R367G) in SCN5A to Be Associated With Familial Cardiac Conduction Disease

Molecular Medicine Reports

Molecular Biology

Cancer Research

Molecular Medicine

English

R222Q Nav1.5 Mutation Associated With a New SCN5A-Related Cardiac Arrhythmia

Biophysical Journal

English

A Novel SCN5A Mutation Associated With Drug Induced Brugada Type ECG

Multidisciplinary

English

Changes in Phenotype and Differentiation Potential of Human Mesenchymal Stem Cells Aging in Vitro

Stem Cell Research and Therapy

Molecular Biology

Molecular Medicine

English

In Vitro and in Vivo Changes in Human Complement Caused by Silage

Environmental Health Perspectives

Occupational Health

English

Pilsicainide Administration Unmasks a Phenotype of Brugada Syndrome in a Patient With Overlap Syndrome Due to the E1784K SCN5A Mutation

Internal Medicine

Internal Medicine

English