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Sarcospan
Development of a High-Throughput Screen to Identify Small Molecule Enhancers of Sarcospan for the Treatment of Duchenne Muscular Dystrophy
Dystrophin Complex Functions As a Scaffold for Signalling Proteins☆
Dystrobrevin Alpha Gene Is a Direct Target of the Vitamin D Receptor in Muscle
Reviewreview Duchenne Muscular Dystrophy and Dystrophin: Pathogenesis and Opportunities for Treatment Third in Molecular Medicine Review Series Kristen J
Governs the Making of Photocopies Or Other Reproductions of Copyrighted Materials
Sarcospan-Dependent Akt Activation Is Required for Utrophin Expression and Muscle Regeneration
Muscle Diseases: the Muscular Dystrophies
The Congenital and Limb-Girdle Muscular Dystrophies Sharpening the Focus, Blurring the Boundaries
Muscular Dystrophies Involving the Dystrophin–Glycoprotein Complex: an Overview of Current Mouse Models Madeleine Durbeej and Kevin P Campbell*
Disrupted Mechanical Stability of the Dystrophin- Glycoprotein Complex Causes Severe Muscular Dystrophy in Sarcospan Transgenic Mice
A Structural Fix For
Generation and Characterization of a Dmdegfp Reporter Mouse As a Tool to Investigate Dystrophin Expression Mina Petkova
Fukutin-Related Protein Associates with the Sarcolemmal Dystrophin
Generation and Characterization of a Dmdegfp Reporter Mouse As a Tool to Investigate Dystrophin Expression
Michelle Parvatiyar: Curriculum Vitae
The Genetic and Molecular Basis of Muscular Dystrophy: Roles of Cell–Matrix Linkage in the Pathogenesis
Fukuyama-Type Congenital Muscular Dystrophy and Defective Glycosylation of A-Dystroglycan Fumiaki Saito and Kiichiro Matsumura
Evolución Clínica Y Recurrencia De Crisis
Top View
Expression-Functional Correlation and Validation of a Surrogate Marker for DAPC Restoration in a Mouse Model of LGMD2E Eric R
A New Model for the Dystrophin Associated Protein Complex in Striated
Gene Transfer Establishes Primacy of Striated Vs. Smooth Muscle Sarcoglycan Complex in Limb-Girdle Muscular Dystrophy
Stabilization of the Cardiac Sarcolemma by Sarcospan Rescues DMD-Associated Cardiomyopathy
Role of Dystroglycan in Limiting Contraction-Induced Injury to the Sarcomeric Cytoskeleton of Mature Skeletal Muscle
Cell-Matrix Adhesion in Muscle Development and Disease Michelle F
Sarcoglycan, the Heart, and Skeletal Muscles: New Treatment, Old Drug?
Reduced Expression of Sarcospan in Muscles of Fukuyama Congenital Muscular Dystrophy
Generation of Desminopathy in Rats Using CRISPR‐Cas9
Nanospan, an Alternatively Spliced Isoform of Sarcospan, Localizes To
The Dystrophin Node As Integrator of Cytoskeletal Organization, Lateral Force Transmission, Fiber Stability and Cellular Signaling in Skeletal Muscle
Limb–Girdle Muscular Dystrophies Michela Guglieri, Volker Straub, Kate Bushby and Hanns Lochmu¨Ller
Datasheet PB9276 Anti-DMD Antibody
Prevention of Cardiomyopathy in Mouse Models Lacking the Smooth Muscle Sarcoglycan-Sarcospan Complex
Regulation of Nicotinic Acetylcholine Receptor Stability at the Mouse Neuromuscular Junction By
Master Regulators of Muscle Atrophy: Role of Costamere Components
High-Throughput Screening Identifies Modulators of Sarcospan That
Dystroglycan and Muscolar Dystrophies Related to the Dystrophin-Glycoprotein Complex