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Dysferlin
Supplementary Data
Characterization of the Dysferlin Protein and Its Binding Partners Reveals Rational Design for Therapeutic Strategies for the Treatment of Dysferlinopathies
New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
Analysis of the Dystrophin Interactome
Molecular Signatures of Membrane Protein Complexes Underlying Muscular Dystrophy*□S
©Ferrata Storti Foundation
Genetic Modifiers of Hereditary Neuromuscular Disorders
Identification of Proteins Interacting with Dysferlin Using the Tandem Affinity Purification Method
Comparative Proteomics Reveals Abnormal Binding of ATGL and Dysferlin on Lipid Droplets from Pressure Overload-Induced Dysfunctional Rat Hearts
Contribution of Dysferlin-Containing Membranes to Membrane Repair in Skeletal Muscle
Dystrophin Deficiency Exacerbates Skeletal Muscle Pathology In
Genetic Ablation of Complement C3 Attenuates Muscle Pathology in Dysferlin-Deficient Mice Renzhi Han,1,2 Ellie M
Muscular Dystrophies Involving the Dystrophin–Glycoprotein Complex: an Overview of Current Mouse Models Madeleine Durbeej and Kevin P Campbell*
Muscular Dystrophy with Marked Dysferlin Deficiency Is Consistently Caused by Primary Dysferlin Gene Mutations
Fatty Acid Metabolism Driven Mitochondrial Bioenergetics Promotes Advanced Developmental Phenotypes in Human Induced Pluripotent Stem Cell Derived Cardiomyocytes
Deficiency of MMP17/MT4-MMP Proteolytic Activity Predisposes to Aortic Aneurysm in Mice
Dysferlin Function in Skeletal Muscle: Possible Pathological Mechanisms and Therapeutical Targets in Dysferlinopathies
Childhood Onset Limb-Girdle Muscular Dystrophies in the Aegean Part of Turkey
Top View
Mitochondria Mediate Cell Membrane Repair and Contribute to Duchenne Muscular Dystrophy
Molecular and Cellular Basis of Calpainopathy (Limb Girdle Muscular Dystrophy Type 2A) ⁎ Irina Kramerova A, Jacques S
Revised Spectrum of Mutations in Sarcoglycanopathies
Protein Studies in Dysferlinopathy Patients Using Llama-Derived Antibody Fragments Selected by Phage Display
Dysferlininahyperckaemicpatien
(12) Patent Application Publication (10) Pub. No.: US 2006/0099578 A1 Wallace Et Al
DYSF Gene Dysferlin
Presence of SARS-Cov-2 Transcripts in the Choroid Plexus of MS and Non-MS Patients with COVID-19
Upregulated IL-1Β in Dysferlin-Deficient Muscle Attenuates Regeneration by Blunting the Response to Pro-Inflammatory Macrophages Tatiana V
Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
Plasma Membrane Protein Identifications from Human Bone Marrow Mesenchymal Stem Cells
Stage-Specific Effects of Notch Activation During Skeletal Myogenesis
A New Model for the Dystrophin Associated Protein Complex in Striated
4Th Annual Dysferlin Conference Report
GRAF1 Deficiency Blunts Sarcolemmal Injury Repair and Exacerbates Cardiac and Skeletal Muscle Pathology in Dystrophin-Deficient Mice Kaitlin C
Supporting Figure Legend Figure S1
Dysferlin and Animal Models for Dysferlinopathy
Clinical and Pathological Characteristics of Four Korean Patients with Limb-Girdle Muscular Dystrophy Type 2B
SUPPLEMENTARY MATERIALS the Inflammatory Cytokine IL-3
Complement Activation in Peritoneal Dialysis–Induced Arteriolopathy
Role of Dystroglycan in Limiting Contraction-Induced Injury to the Sarcomeric Cytoskeleton of Mature Skeletal Muscle
Therapeutic Possibilities in the Autosomal Recessive Limb-Girdle Muscular Dystrophies
Gene Therapy for Muscular Dystrophy
Dysferlin-Mediated Membrane Repair Protects the Heart from Stress
Stage-Specific Effects of Notch Activation During Skeletal Myogenesis
Genetics of Nonalcoholic Fatty Liver Disease: from Pathogenesis to Therapeutics
The Dystrophin Node As Integrator of Cytoskeletal Organization, Lateral Force Transmission, Fiber Stability and Cellular Signaling in Skeletal Muscle
Reappraisal of Human HOG and MO3.13 Cell Lines As a Model to Study Oligodendrocyte Functioning
Full Text (PDF)
Dysferlin and Muscle Membrane Repair Renzhi Han and Kevin P Campbell
Expression Profiling of Novel Iron-Related Genes in Mouse Models of Iron Overload
Gether of the Neurotransmitter Acetylcholine (Ach) Into the with the Terminal Cisternae of the Sarcoplasmic Retic- Neuromuscular Junction
Our Project Is to Determine the Potential Contribution Of
How Myelin-Specific CD8 T Cells Contribute to CNS Autoimmunity
Protein Hypercitrullination, a Basic Mechanism in Demyelinating Diseases
Responsive Nuclear Proteins in Collecting Duct Cells
Mendelian Disorders Among Jews
Efficient Exon Skipping of SGCG Mutations Mediated by Phosphorodiamidate Morpholino Oligomers
The Ubiquitin Ligase Tripartite-Motif-Protein 32 Is Induced