Pages that link to "Q42108368"
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The following pages link to Multiplex Western blotting system for the analysis of muscular dystrophy proteins (Q42108368):
Displaying 50 items.
- AHNAK, a novel component of the dysferlin protein complex, redistributes to the cytoplasm with dysferlin during skeletal muscle regeneration (Q24337859) (← links)
- Immunohistochemical analysis of calpain 3: advantages and limitations in diagnosing LGMD2A (Q24339386) (← links)
- The importance of genetic diagnosis for Duchenne muscular dystrophy (Q26769701) (← links)
- Identification of reference proteins for Western blot analyses in mouse model systems of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) toxicity (Q27334657) (← links)
- Muscle inflammation and MHC class I up-regulation in muscular dystrophy with lack of dysferlin: an immunopathological study (Q28205102) (← links)
- Murine muscle engineered from dermal precursors: an in vitro model for skeletal muscle generation, degeneration, and fatty infiltration (Q30560376) (← links)
- Comparison of dysferlin expression in human skeletal muscle with that in monocytes for the diagnosis of dysferlin myopathy. (Q31043843) (← links)
- Evaluation of the dystrophin-glycoprotein complex, alpha-actinin, dysferlin and calpain 3 in an autosomal recessive muscular dystrophy in Labrador retrievers (Q31882212) (← links)
- Differential expression of synapsin in visual neurons of the locust Schistocerca gregaria (Q33208494) (← links)
- Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population (Q33685609) (← links)
- Making sense of the limb-girdle muscular dystrophies (Q33701932) (← links)
- Diagnostic protein expression in human muscle biopsies (Q33891334) (← links)
- Chimeric snRNA molecules carrying antisense sequences against the splice junctions of exon 51 of the dystrophin pre-mRNA induce exon skipping and restoration of a dystrophin synthesis in Delta 48-50 DMD cells (Q34035676) (← links)
- New aspects on patients affected by dysferlin deficient muscular dystrophy (Q34289381) (← links)
- From proteins to genes: immunoanalysis in the diagnosis of muscular dystrophies (Q35166268) (← links)
- Phenotypic heterogeneity in British patients with a founder mutation in the FHL1 gene (Q35304215) (← links)
- A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families (Q35434715) (← links)
- Dysferlinopathy course and sportive activity: clues for possible treatment (Q35607518) (← links)
- Restoration of the dystrophin-associated glycoprotein complex after exon skipping therapy in Duchenne muscular dystrophy (Q35750055) (← links)
- Microglial cell activation is a source of metalloproteinase generation during hemorrhagic transformation. (Q35939162) (← links)
- Titin mutation segregates with hereditary myopathy with early respiratory failure (Q35986692) (← links)
- Signaling satellite-cell activation in skeletal muscle: markers, models, stretch, and potential alternate pathways (Q35997374) (← links)
- Analysis of calpain-3 protein in muscle biopsies of different muscular dystrophies from India. (Q36134506) (← links)
- A new titinopathy: Childhood-juvenile onset Emery-Dreifuss-like phenotype without cardiomyopathy (Q36405878) (← links)
- Novel deletion of lysine 7 expands the clinical, histopathological and genetic spectrum of TPM2-related myopathies. (Q36611392) (← links)
- In vivo gene editing in dystrophic mouse muscle and muscle stem cells (Q37045850) (← links)
- Duchenne and Becker muscular dystrophy: contribution of a molecular and immunohistochemical analysis in diagnosis in Morocco (Q37196723) (← links)
- Role of dystroglycan in limiting contraction-induced injury to the sarcomeric cytoskeleton of mature skeletal muscle. (Q37304803) (← links)
- Tadalafil alleviates muscle ischemia in patients with Becker muscular dystrophy. (Q37604365) (← links)
- Ovarian cancer proteomics: Many technologies one goal (Q37817189) (← links)
- Molecular diagnosis of muscular dystrophies, focused on limb girdle muscular dystrophies (Q38089840) (← links)
- Protein and genetic diagnosis of limb girdle muscular dystrophy type 2A: The yield and the pitfalls (Q38434135) (← links)
- Abnormalities in alpha-dystroglycan expression in MDC1C and LGMD2I muscular dystrophies (Q38584853) (← links)
- Progress and challenges in diagnosis of dysferlinopathy (Q38921880) (← links)
- Hyperckemia and myalgia are common presentations of anoctamin-5-related myopathy in French patients (Q38967024) (← links)
- Pharmacological inhibition of HSP90 activity negatively modulates myogenic differentiation and cell survival in C2C12 cells (Q39510533) (← links)
- Spatial and temporal expression of hypoxia-inducible factor-1α during myogenesis in vivo and in vitro (Q39642460) (← links)
- Sarcolemmal neuronal nitric oxide synthase defect in limb-girdle muscular dystrophy: an adverse modulating factor in the disease course? (Q39994932) (← links)
- Disruption of dystroglycan axis by beta-dystroglycan processing in cardiomyopathic hamster muscle (Q40606913) (← links)
- Intraarterial injection of muscle-derived CD34(+)Sca-1(+) stem cells restores dystrophin in mdx mice. (Q40818700) (← links)
- Short (16-mer) locked nucleic acid splice-switching oligonucleotides restore dystrophin production in Duchenne Muscular Dystrophy myotubes (Q41106058) (← links)
- Deletion of exon 26 of the dystrophin gene is associated with a mild Becker muscular dystrophy phenotype. (Q41855877) (← links)
- Prednisolone treatment does not interfere with 2'-O-methyl phosphorothioate antisense-mediated exon skipping in Duchenne muscular dystrophy (Q42587467) (← links)
- Dystrophinopathy caused by mid-intronic substitutions activating cryptic exons in the DMD gene (Q42614868) (← links)
- Muscle histopathology in today's era of molecular genetics: Role and limitations (Q43123811) (← links)
- Anoctamin 5 muscular dystrophy in Denmark: prevalence, genotypes, phenotypes, cardiac findings, and muscle protein expression (Q44039213) (← links)
- The phenotype of limb-girdle muscular dystrophy type 2I (Q44411539) (← links)
- Protein and gene analyses of dysferlinopathy in a large group of Japanese muscular dystrophy patients (Q44454445) (← links)
- Pure quadriceps myopathy in two sisters (Q44489209) (← links)
- Utrophin is lacking at the neuromuscular junctions in the extraocular muscles of normal cat: artefact or true? (Q45281544) (← links)