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MYH7
Genetic Mutations and Mechanisms in Dilated Cardiomyopathy
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Unequal Allelic Expression of Wild-Type and Mutated B-Myosin in Familial Hypertrophic Cardiomyopathy
Genome Editing for the Understanding and Treatment of Inherited Cardiomyopathies
Hypertrophic Cardiomyopathy (HCM)
Cardiogenetics Testing Reference Guide December 2018
Microrna Regulatory Pathways in the Control of the Actin–Myosin Cytoskeleton
Sarcomeres Regulate Murine Cardiomyocyte Maturation Through MRTF-SRF Signaling
Illuminating the Divergent Role of Filamin C Mutations in Human Cardiomyopathy
Genetic Cardiomyopathies: the Lesson Learned from Hipscs
A Novel Pathogenicity and Phenotype Predictor for Functional Evaluation Of
MYH7 Gene-Related Mutation P.V878L Identified in a Chinese Family with Hypertrophic Cardiomyopathy
MYH7 - Hypertrophic Cardiomyopathy Testing
MYH7 Gene Myosin Heavy Chain 7
Advanced Fiber Type-Specific Protein Profiles Derived from Adult Murine
Microrna-223 Prevents Cardiomyocyte Hypertrophy by Targeting Cardiac Troponin I-Interacting Kinase
Genetic Restrictive Cardiomyopathy: Causes and Consequences—An Integrative Approach
Skeletal Muscle Gene Expression in Long-Term Endurance and Resistance Trained Elderly
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Two Novel MYH7 Proline Substitutions Cause Laing Distal Myopathy-Like Phenotypes with Variable Expressivity and Neck Extensor Co
Genome-Wide Analysis of Organ-Preferential Metastasis of Human Small Cell Lung Cancer in Mice
Cardiovascular Diseases Genetic Testing Program Information
Quantitative Proteome Profiling of Dystrophic Dog Skeletal Muscle
Promoter Interactome of Human Embryonic Stem Cell-Derived Cardiomyocytes Connects GWAS Regions to Cardiac Gene Networks
Childhood Onset
Identifying Cardiac Actinin Interactomes Reveals Sarcomere Crosstalk with RNA-Binding Proteins
CRISPR/Cas9 Editing in Human Pluripotent Stem Cell-Cardiomyocytes Highlights Arrhythmias, Hypocontractility, and Energy Depletio
A Novel Custom Resequencing Array for Dilated Cardiomyopathy Rebekah S
Identifying Dynamic Protein and RNA Proximity Interaction Networks of Actinin Reveals RNA
Genetic Determinants of Clinical Phenotype in Hypertrophic Cardiomyopathy Lazar Velicki1,2*† , Djordje G
Clinical Features, Spectrum of Causal Genetic Mutations and Outcome Of
Revista Española De Cardiología Lamounier Junior A, Et Al
Supplemental Table 1 Genes Up-Regulated (>2.0) in Stat3
Double Heterozygosity for Mutations in the Β-Myosin Heavy Chain and In
Adult Human Cardiac Stem Cell Supplementation Effectively Increases Contractile Function and Maturation in Human Engineered Cardiac Tissues Jack F
One Third of Danish Hypertrophic Cardiomyopathy Patients Have Mutations in MYH7 Rod Region
A New Model for the Dystrophin Associated Protein Complex in Striated