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 Gene Dystrophin Protein Mouse Exon Syndrome Cardiomyopathy Zygosity Phenotype Myopathy Muscular dystrophy DNA Polymerase chain reaction Messenger RNA Acid Western blot Apoptosis Enzyme inhibitor Mutation Obesity Hypertension Ejection fraction Echocardiography Single-nucleotide polymorphism Allele
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Publications tagged with this subject: 39

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1. Translocation of molecular chaperones to the titin springs is common in skeletal myopathy patients and affects sarcomere function

2. Development Aspects of Zebrafish Myotendinous Junction: a Model System for Understanding Muscle Basement Membrane Formation and Failure

3. Cardiac profile of asymptomatic children with Becker and Duchenne muscular dystrophy under treatment with steroids and with/without perindopril

4. Chest Wall Kinematics Using Triangular Cosserat Point Elements in Healthy and Neuromuscular Subjects

5. International Society of Sports Nutrition position stand: safety and efficacy of creatine supplementation in exercise, sport, and medicine

6. Normal and altered pre-mRNA processing in the DMD gene

7. Occurrence of Emery-Dreifuss muscular dystrophy in a rural setting of Cameroon: a case report and review of the literature

8. Growth plate injury at the base of the coracoid: MRI features

9. Present Uses, Future Applications, and Technical Underpinnings of Electrical Impedance Myography

10. The role of LMNA mutations in myogenic differentiation of C2C12 and primary satellite cells

11. The pro-fibrotic connective tissue growth factor (CTGF/CCN2) correlates with the number of necrotic-regenerative foci in dystrophic muscle

12. Origin of dystrophin gene deletions in Duchenne and Becker muscular dystrophy patients from Ukraine

13. Identification of a novel DMD duplication identified by a combination of MLPA and targeted exome sequencing

14. SMCHD1 regulates a limited set of gene clusters on autosomal chromosomes

15. MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from India

16. Current status and future prospect of FSHD region gene 1

17. Effects of omega-3 on matrix metalloproteinase-9, myoblast transplantation and satellite cell activation in dystrophin-deficient muscle fibers

18. Skeletal muscle secretome in Duchenne muscular dystrophy: a pivotal anti-inflammatory role of adiponectin

19. Expression patterns of FSHD-causing DUX4 and myogenic transcription factors PAX3 and PAX7 are spatially distinct in differentiating human stem cell cultures

20. Authentication of collagen VI antibodies

21. GRMD cardiac and skeletal muscle metabolism gene profiles are distinct

22. A rare subclinical or mild type of Becker muscular dystrophy caused by a single exon 48 deletion of the dystrophin gene

23. Maximum inspiratory pressure as a clinically meaningful trial endpoint for neuromuscular diseases: a comprehensive review of the literature

24. Quantifying fat replacement of muscle by quantitative MRI in muscular dystrophy

25. Tailor-made management of thoracic scoliosis with cervical hyperextension in muscular dystrophy

26. The golden retriever model of Duchenne muscular dystrophy

27. Surgical correction of hyperlordosis in facioscapulohumeral muscular dystrophy: A case report

28. Serial prenatal and postnatal MRI of dystroglycanopathy in a patient with familial B3GALNT2 mutation

29. Capture-recapture methodology to study rare conditions using surveillance data for fragile X syndrome and muscular dystrophy

30. Comparison between sEMG and force as control interfaces to support planar arm movements in adults with Duchenne: a feasibility study

31. Gait characterization in golden retriever muscular dystrophy dogs using linear discriminant analysis

32. Elevated Myocardial Extracellular Volume Fraction in Duchenne Muscular Dystrophy

33. Treatment with soluble activin type IIB-receptor improves bone mass and strength in a mouse model of Duchenne muscular dystrophy

34. RIG-I expression in perifascicular myofibers is a reliable biomarker of dermatomyositis

35. Eplerenone for early cardiomyopathy in Duchenne muscular dystrophy: results of a two-year open-label extension trial

36. Large is required for normal astrocyte migration and retinal vasculature development

37. Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan

38. Biomarkers of Musculoskeletal Disorders

39. Therapeutic Gene Editing in Muscles and Muscle Stem Cells


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