DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» Sarcoglycan
Sarcoglycan
Γ-Sarcoglycan Deficiency Increases Cell Contractility, Apoptosis And
Further Evidence for the Organisation of the Four Sarcoglycans Proteins Within the Dystrophin–Glycoprotein Complex
Anti-SGCG / Gamma Sarcoglycan Antibody (ARG41710)
Big, Bad Hearts: from Flies to Man
Genetic Modifiers of Hereditary Neuromuscular Disorders
Sarcoglycan a Mutation in Miniature Dachshund Dogs Causes Limb-Girdle Muscular Dystrophy 2D
Validación Y Estudio De La Implicación De Los Genes Adrbk2, Adrb1, Adra2b, Axin 2, Atp6v1c1 Y Atp6v0e En El Carcinoma Oral De
Pigs with δ-Sarcoglycan Deficiency Exhibit Traits of Genetic
Muscular Dystrophies Involving the Dystrophin–Glycoprotein Complex: an Overview of Current Mouse Models Madeleine Durbeej and Kevin P Campbell*
Dynamic Changes in the Subcellular Localization of Drosophila Β-Sarcoglycan During the Cell Cycle
Factors Regulating the Function and Assembly of the Sarcoglycan Complex in Brain
Childhood Onset Limb-Girdle Muscular Dystrophies in the Aegean Part of Turkey
The Role of Delta Sarcoglycan in Dystrophin-Glycoprotein Complex Function in Cardiac Muscle
Guía De Práctica Clínica (Anexos)
Revised Spectrum of Mutations in Sarcoglycanopathies
The Role of Calcium and Calcium/Calmodulin-Dependent Kinases in Skeletal Muscle Plasticity and Mitochondrial Biogenesis
Mutations in the Human Δ-Sarcoglycan Gene in Familial and Sporadic Dilated Cardiomyopathy
Perfiles De Expresión Génica De Los Tumores De Mama Hereditarios
Top View
A Gene-Edited Mouse Model of Limb-Girdle Muscular Dystrophy 2C for Testing Exon Skipping Alexis R
Genetics of Sarcoglycan Assembly and Function 2537
Skeletal Muscle Mitochondria Dysfunction in Genetic Neuromuscular Disorders with Cardiac Phenotype
2019 Wellstone Family Conference Updates, Kdm Copy
A New Model for the Dystrophin Associated Protein Complex in Striated
Adeno-Associated Virus Mediated Β-Sarcoglycan Gene Replacement Therapy for the Treatment of Limb Girdle Muscular Dystrophy Type 2E
Review Increasing Complexity of the Dystrophin-Associated Protein Complex Jonathon M
Sarcoglycan Are Not Muscle-Specific
Gene Therapy for Muscular Dystrophy
Sarcoglycan, the Heart, and Skeletal Muscles: New Treatment, Old Drug?
Role for Α-Dystrobrevin in the Pathogenesis of Dystrophin-Dependent Muscular Dystrophies
The Dystrophin Node As Integrator of Cytoskeletal Organization, Lateral Force Transmission, Fiber Stability and Cellular Signaling in Skeletal Muscle
Muscle Degeneration Without Mechanical Injury in Sarcoglycan Deficiency
Sarcoglycan a Mutation in Miniature Dachshund Dogs Causes Limb-Girdle Muscular Dystrophy 2D James R
Prevention of Cardiomyopathy in Mouse Models Lacking the Smooth Muscle Sarcoglycan-Sarcospan Complex
The Sarcoglycan Complex in Limb-Girdle Muscular Dystrophy
SGCG Gene Sarcoglycan Gamma
Genetic Compensation for Sarcoglycan Loss by Integrin Α7β1 in Muscle
Dystrophin Protein Complex Assembly in Living Cells
Efficient Exon Skipping of SGCG Mutations Mediated by Phosphorodiamidate Morpholino Oligomers
Disruption of Heart Sarcoglycan Complex and Severe Cardiomyopathy Caused by Β Sarcoglycan Mutations
Genetic Analysis of Α7β1 Integrin Function in Skeletal Muscle
Systemic Dose-Finding Study with AAV-Mediated Γ-Sarcoglycan Gene Therapy for Treatment of Muscle Deficits in LGMD2C Mice Young-Eun Seo, Amber N