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DTNA
Genetic Mutations and Mechanisms in Dilated Cardiomyopathy
Integrative Analyses Identify Potential Key Genes and Pathways in Keshan
Disrupted Mechanobiology Links the Molecular and Cellular Phenotypes
Dilated Cardiomyopathy Caused by Truncating Titin Variants
New Insights in RBM20 Cardiomyopathy
Individual Protomers of a G Protein-Coupled Receptor Dimer Integrate Distinct Functional Modules
Distinct Fiber Type Signature in Mouse Muscles Expressing a Mutant Lamin a Responsible for Congenital Muscular Dystrophy in a Patient
Analysis of the Dystrophin Interactome
Molecular Signatures of Membrane Protein Complexes Underlying Muscular Dystrophy*□S
Genetic Architecture of Recent-Onset Dilated Cardiomyopathy in Moravian
Humanizing the Mdx Mouse Model of DMD: the Long and the Short of It
Dystrophin Insufficiency Causes Selective Muscle Histopathology and Loss of Dystrophin-Glycoprotein Complex Assembly in Pig Skeletal Muscle
Muscle-Specific Mis-Splicing and Heart Disease Exemplified by RBM20
DTNA Rabbit Pab
Anti-Dystrobrevin-Alpha
Α-Dystrobrevin-1 Recruits Α-Catulin to the Α1d- Adrenergic Receptor/Dystrophin-Associated Protein Complex Signalosome
Evolving Approaches to Genetic Evaluation of Specific Cardiomyopathies
Sudden Cardiac Death in Young Athletes: Literature Review Of
Top View
Cardiomyopathy and Arrhythmia Panel, Sequencing and Deletion/Duplication ARUP Test Code 2010183 Cardiomyopathy/Arrhythmia Panel Specimen Whole Blood
Inherited Cardiovascular Diseases and Sudden Cardiac Death to Provide an Exhaustive Study of Genes
Supplementary Appendix
Advancing Molecular Diagnostics in Sudden Unexplained Deaths
Stage-Specific Effects of Notch Activation During Skeletal Myogenesis
A New Model for the Dystrophin Associated Protein Complex in Striated
Dystrobrevin Alpha (DTNA) Mouse Monoclonal Antibody [Clone ID: OTI1A2] Product Data
Genetic Basis of Hypertrophic Cardiomyopathy
Dystrobrevin Alpha Gene Is a Direct Target of the Vitamin D Receptor in Muscle
Transcriptional Network Analysis of Human Astrocytic Endfoot Genes Reveals Region-Specific Associations with Dementia Status
Titin: an Analysis of Genetic Variation and Cardiac Phenotype
Functional Analysis of a Gene-Edited Mouse Model to Gain Insights Into
Stage-Specific Effects of Notch Activation During Skeletal Myogenesis
A Novel Titin Truncation Variant Linked to Familial Dilated
Cardiomyopathy and Arrhythmia Panel, Sequencing and Deletion/Duplication
The Role of Alpha-Dystrobrevin in Striated Muscle
UNIVERSITY of CALIFORNIA, SAN DIEGO Systems Biology
An Overview of Alternative Splicing Defects Implicated in Myotonic Dystrophy Type I