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Proceedings of the National Academy of Sciences - PNAS, ISSN 0027-8424, 12/2012, Volume 109, Issue 50, pp. 20614 - 20619
Duchenne muscular dystrophy (DMD) is a devastating genetic muscular disorder of childhood marked by progressive debilitating muscle weakness and wasting, and ultimately death in the second or third decade of life... 
Artificial satellites | Plasmids | Duchenne muscular dystrophy | Stem cells | Muscles | Electroporation | Muscle fibers | Skeletal muscle | Hypertrophy | Myoblasts | Noncanonical Wnt signaling | REGENERATION | MULTIDISCIPLINARY SCIENCES | MOUSE | SUSCEPTIBILITY | INJURY | SATELLITE STEM-CELLS | MDX MICE | DAMAGE | noncanonical Wnt signaling | SKELETAL-MUSCLE | CONTRACTION | PATHWAY | skeletal muscle | Genetic Therapy | Muscular Dystrophy, Animal - genetics | Muscular Dystrophy, Animal - drug therapy | Muscular Dystrophy, Animal - physiopathology | Humans | Male | RNA, Messenger - metabolism | Muscular Dystrophy, Animal - pathology | Gene Knockdown Techniques | Wnt Proteins - genetics | Mice, Inbred mdx | Plasmids - genetics | Electrochemotherapy | MEF2 Transcription Factors | Myogenic Regulatory Factors - genetics | Signal Transduction | Mice, Inbred C57BL | RNA, Messenger - genetics | Myogenic Regulatory Factors - metabolism | Wnt Proteins - therapeutic use | Regeneration - physiology | Animals | Muscle Contraction - physiology | Muscle, Skeletal - physiopathology | Mice | Wnt Proteins - physiology | Muscle, Skeletal - pathology | Plasmids - administration & dosage | Physiological aspects | Care and treatment | Rapamycin | Health aspects | Muscular dystrophy | Biological Sciences
Journal Article
PloS one, ISSN 1932-6203, 2014, Volume 9, Issue 10, p. e110371
A few animal models of Duchenne muscular dystrophy (DMD) are available, large ones such as pigs or dogs being expensive and difficult to handle. Mdx... 
MDX | PREDICTS | ZEBRAFISH | EVOLUTION | GENE | MULTIDISCIPLINARY SCIENCES | ZINC-FINGER | CALCIUM | EMBRYO MICROINJECTION | GENERATION | KNOCKOUT RATS | Exons | Male | Muscle, Skeletal - metabolism | RNA, Messenger - metabolism | Muscle Weakness - genetics | Muscular Dystrophy, Duchenne - physiopathology | Base Sequence | Dystrophin - deficiency | Gene Deletion | Myocardium - metabolism | Muscular Dystrophy, Animal | Ventricular Remodeling - genetics | Female | Dystrophin - metabolism | Disease Models, Animal | Gene Targeting | Gene Expression | Creatine Kinase - blood | RNA, Messenger - genetics | Rats | Muscular Dystrophy, Duchenne - pathology | Myocardium - pathology | Animals | Dystrophin - genetics | Fibrosis | Muscular Dystrophy, Duchenne - metabolism | Muscle, Skeletal - pathology | Muscular Dystrophy, Duchenne - genetics | Mutation | Immunohistochemistry | Chemical properties | Dystrophin | Duchenne muscular dystrophy | Utrophin | Heart | Animal models | Adipose tissue | Cardiomyopathy | Motor activity | Muscular dystrophy | Proteins | Immunology | Rodents | Duchenne's muscular dystrophy | Gangrene | Diaphragm (anatomy) | Muscular strength | Lesions | Pigs | Echocardiography | Life expectancy | Abnormalities | Muscles | Thorax | Disease control | Regeneration | Musculoskeletal system | Dilated cardiomyopathy | Genetic engineering | Mice | Infiltration | Dystrophy | Diaphragm | Laboratory animals | Life Sciences | Human health and pathology
Journal Article
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 03/2011, Volume 364, Issue 10, pp. 939 - 946
.... Muscular dystrophies are genetic diseases characterized by weakness and progressive degeneration of skeletal muscle... 
Phenotype | Animals | Muscular Dystrophies, Limb-Girdle - genetics | Pedigree | Humans | Dystroglycans - genetics | Female | Mice | Mutation, Missense | Sequence Analysis, DNA | Disease Models, Animal
Journal Article
2011, Methods in molecular biology, ISBN 9781617379826, Volume 709., xiii, 382
Book
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 2014, Volume 111, Issue 16, pp. 6004 - 6009
Journal Article
Journal Article
Journal Article
Mammalian genome, ISSN 0938-8990, 2012, Volume 23, Issue 1-2, pp. 85 - 108
Journal Article
American journal of human genetics, ISSN 0002-9297, 03/2013, Volume 92, Issue 3, pp. 354 - 365
Journal Article
Journal Article