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MYL2
Identification of the Binding Partners for Hspb2 and Cryab Reveals
Genetic Mutations and Mechanisms in Dilated Cardiomyopathy
Inhibition of Β-Catenin Signaling Respecifies Anterior-Like Endothelium Into Beating Human Cardiomyocytes Nathan J
Transcriptomic Uniqueness and Commonality of the Ion Channels and Transporters in the Four Heart Chambers Sanda Iacobas1, Bogdan Amuzescu2 & Dumitru A
The Role of Wnt/Β-Catenin Antagonists - Sclerostin and DKK1 - in Bone Homeostasis and Mechanotransduction
A Concise Review of Human Brain Methylome During Aging and Neurodegenerative Diseases
Understanding Lamin A/C and Its Roles in Disease
Coverage and Diagnostic Yield of Whole Exome Sequencing for the Evaluation of Cases with Dilated and Hypertrophic Cardiomyopathy
PKM2 Phosphorylates MLC2 and Regulates Cytokinesis of Tumour Cells
Genetic Testing for Inherited Cardiomyopathies and Channelopathies AHS – M2025
Proteomics Study on the Effect of Silybin on Cardiomyopathy in Obese
Prevalence and Distribution of Sarcomeric Gene Mutations in Japanese Patients with Familial Hypertrophic Cardiomyopathy
The Role of Sarcomere Gene Mutations in Patients with Idiopathic Dilated Cardiomyopathy
Mutations in the Cardiac Troponin T Gene Show Various Prognoses in Japanese Patients with Hypertrophic Cardiomyopathy
Fatty Acid Metabolism Driven Mitochondrial Bioenergetics Promotes Advanced Developmental Phenotypes in Human Induced Pluripotent Stem Cell Derived Cardiomyocytes
Long-Term Outcomes of Pediatric-Onset Hypertrophic Cardiomyopathy and Age-Specific Risk Factors for Lethal Arrhythmic Events
Pivotal Role of the Muscle-Contraction Pathway in Cryptorchidism And
Systematic Analysis of the Regulatory and Essential Myosin Light Chain Genes: Genetic Variants and Mutations in Hypertrophic Cardiomyopathy
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Labaccess Partnership (Lap) Program
Robust Cardiomyocyte Differentiation from Human Pluripotent Stem Cells Via Temporal Modulation of Canonical Wnt Signaling
Transcriptomic and Proteomic Analysis of Hemidactylus Frenatus During Initial Stages of Tail Regeneration Sai Pawan Nagumantri, Sarena Banu & Mohammed M
Identifying Dynamic Protein and RNA Proximity Interaction Networks of Actinin Reveals RNA
Mono- and Bi-Allelic Protein Truncating Variants in Alpha-Actinin 2 Cause Cardiomyopathy Through Distinct Mechanisms
MYL2-Associated Congenital Fiber-Type Disproportion and Cardiomyopathy with Variants In
Electronic Letter Myosin Light Chain Mutations in Familial Hypertrophic Cardiomyopathy
Differentiation of Human Cardiac Atrial Appendage Stem Cells Into Adult
A Novel Approach to Identification of Diagnostic Markers In
MYL2 – Associated Hypertrophic Cardiomyopathy
Gene Expression Profile in Similar Tissues Using Transcriptome Sequencing Data of Whole-Body Horse Skeletal Muscle
Adult Human Cardiac Stem Cell Supplementation Effectively Increases Contractile Function and Maturation in Human Engineered Cardiac Tissues Jack F
Uric Acid: a Potent Molecular Contributor to Pluripotent Stem Cell Cardiac Differentiation Via Mesoderm Specification
Isolation of Contractile Cardiomyocytes from Human Pluripotent Stem-Cell-Derived Cardiomyogenic Cultures Using a Human NCX1-EGFP Reporter
Mutation P.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy
Yield of Rare Variants Detected by Targeted Next-Generation Sequencing in a Cohort of Romanian Index Patients with Hypertrophic Cardiomyopathy
Denervation Protects Limbs from Inflammatory Arthritis Via an Impact on the Microvasculature
Geneseq®: Cardio