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MYH6
FLNC Missense Variants in Familial Noncompaction Cardiomyopathy
Genetic Mutations and Mechanisms in Dilated Cardiomyopathy
A Rare Missense Mutation in MYH6 Confers High Risk of Coarctation of the Aorta
A CRISPR Path to Engineering New Genetic Mouse Models for Cardiovascular Research
SUPPLEMENTAL MATERIAL Data S1
Catenin Regulates Cardiac Energy Metabolism in Sedentary and Trained Mice
Towards Development of a Statistical Framework to Evaluate Myotonic Dystrophy Type 1 Mrna Biomarkers in the Context of a Clinical Trial
Use of Biotinylated Ubiquitin for Analysis of Rat Brain Mitochondrial Proteome and Interactome
Microrna-223 Prevents Cardiomyocyte Hypertrophy by Targeting Cardiac Troponin I-Interacting Kinase
Region of Interest Analysis Using Mass Spectrometry Imaging Of
Genotype-Related Clinical Characteristics and Myocardial Fibrosis and Their Association with Prognosis in Hypertrophic Cardiomyopathy
The Use of Genetic Analyses and Functional Assays for the Interpretation of Rare Variants in Pediatric Heart Disease
Gender-Specific Molecular and Clinical Features Underlie Malignant Pleural Mesothelioma
Cardiovascular Diseases Genetic Testing Program Information
Early Cardiac Inflammation As a Driver of Murine Model of Arrhythmogenic Cardiomyopathy
PRC2 Directly Methylates GATA4 and Represses Its Transcriptional Activity
Bioinformatics-Based Study to Detect Chemical Compounds That Show Potential As Treatments for Pulmonary Thromboembolism
Identifying Cardiac Actinin Interactomes Reveals Sarcomere Crosstalk with RNA-Binding Proteins
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Existing Cardiomyocytes Generate Cardiomyocytes at a Low Rate After Birth in Mice
CRISPR/Cas9 Editing in Human Pluripotent Stem Cell-Cardiomyocytes Highlights Arrhythmias, Hypocontractility, and Energy Depletio
Myosin 7B Is a Regulatory Long Noncoding RNA (Lncmyh7b) in the Human Heart
Proteomic and Transcriptomic Analysis of Lung Tissue in OVA-Challenged Mice
Identifying Dynamic Protein and RNA Proximity Interaction Networks of Actinin Reveals RNA
Differential Gene Expression Analysis of HNSCC Tumors Deciphered Tobacco Dependent and Independent Molecular Signatures
Identification of Novel Causative Genes for Colorectal Adenomatous Polyposis
CARDIOVASCULAR DISEASES TESTING REQUISITION All Information Must Be Completed Before Sample Can Be Processed PATIENT INFORMATION ETHNIC/RACIAL BACKGROUND (Choose All)
Phosphodiesterase Inhibitors Revert Axonal Dystrophy in Friedreich's
BACKGROUND METHODS REFERENCES MYH6 C.2161C>T
Genetic Complexity in Hypertrophic Cardiomyopathy Revealed by High-Throughput Sequencing
Analysis of 51 Proposed Hypertrophic Cardiomyopathy Genes from Genome Sequencing Data in Sarcomere Negative Cases Has Negligible Diagnostic Yield
Mutation P.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy
Molecular and Cellular Phenotypic Profiles of Gastric Noninvasive Neoplasia
MYH6 Gene Myosin Heavy Chain 6
Souidi Sleiman Et Al. 1
Regulation of Cytoplasmic Dynein by LIS1 and Adenomatous Polyposis Coli Timothy Joshua Hines University of South Carolina
Role of Serum Response Factor in the Pathogenesis of Disease Joseph M Miano