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Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2012, Volume 7, Issue 1, pp. e29904 - e29904
Background: The dystrophin gene, which is mutated in Duchenne muscular dystrophy (DMD), encodes a large cytoskeletal protein present in muscle fibers. While... 
AORTIC-CELLS | CELLS IN-VITRO | GLYCOPROTEIN COMPLEX | BIOLOGY | MUSCULAR-DYSTROPHY | EXTRACELLULAR-MATRIX | PROLIFERATION | SARCOGLYCAN-SARCOSPAN COMPLEX | LAMININ ISOFORMS | EXPRESSION | VASCULAR SMOOTH-MUSCLE | Muscular Dystrophy, Animal - genetics | Up-Regulation | Cell Proliferation | Muscle, Smooth, Vascular - metabolism | Vascular System Injuries - genetics | Myocytes, Smooth Muscle - pathology | Muscular Dystrophy, Animal - complications | Muscular Dystrophy, Animal - pathology | Vascular System Injuries - pathology | Dystrophin - physiology | Neointima - genetics | Dystrophin - deficiency | Mice, Inbred mdx | Muscular Dystrophy, Animal - metabolism | Dystrophin - metabolism | Myocytes, Smooth Muscle - metabolism | Mice, Inbred C57BL | Cells, Cultured | Organ Size | Muscular Dystrophy, Duchenne - pathology | Muscular Dystrophy, Duchenne - complications | Neointima - metabolism | Vascular System Injuries - metabolism | Muscle, Smooth, Vascular - pathology | Animals | Dystrophin - genetics | Neointima - pathology | Mice | Muscular Dystrophy, Duchenne - metabolism | Muscular Dystrophy, Duchenne - genetics | Muscles | RNA | Dystrophin | Analysis | Utrophin | Genes | Cell proliferation | Cell culture | Pathogenesis | Science | Smooth muscle | Muscular dystrophy | Cell adhesion & migration | Cell growth | Transgenic animals | Rodents | Duchenne's muscular dystrophy | Extracellular matrix | Carotid artery | Lesions | Injuries | Injury analysis | Thickening | Dystroglycan | Gene expression | Skeletal muscle | Musculoskeletal system | Cytoskeleton | Ligands | Mutation | Dystrophy | Circulatory system | Cell migration | Veins & arteries | Index Medicus | Cell and Molecular Biology | Basic Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Cell- och molekylärbiologi | Medicinska och farmaceutiska grundvetenskaper
Journal Article
Lancet, The, ISSN 0140-6736, 2011, Volume 378, Issue 9791, pp. 595 - 605
Journal Article
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 5, pp. e19189 - e19189
Journal Article
Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 01/2017, Volume 58, Issue 1, pp. 343 - 352
Journal Article
Journal Article
Molecular Cell, ISSN 1097-2765, 11/2017, Volume 68, Issue 3, pp. 479 - 490.e5
Transcription of expanded microsatellite repeats is associated with multiple human diseases, including myotonic dystrophy, Fuchs endothelial corneal dystrophy,... 
myotonic dystrophy | CRISPR | RNA toxicity | transcription | microsatellite repeat disease | Cas9 | amyotrophic lateral sclerosis | RNA polymerase II | C9ORF72/ALS/FTD | STAPHYLOCOCCUS-AUREUS CAS9 | STEM-CELLS | MUSCLEBLIND PROTEINS | SMALL-MOLECULE | BIOCHEMISTRY & MOLECULAR BIOLOGY | MOUSE MODEL | MUSCULAR-DYSTROPHY | GENE-EXPRESSION | MYOTONIC-DYSTROPHY | RNA FOCI | HUNTINGTON-DISEASE | CELL BIOLOGY | C9orf72 Protein - genetics | Dependovirus - genetics | Myotonic Dystrophy - metabolism | ran GTP-Binding Protein - genetics | Alternative Splicing | RNA, Guide - genetics | CD24 Antigen - metabolism | Humans | Male | Chloride Channels - genetics | Endonucleases - metabolism | Myoblasts - metabolism | Myotonic Dystrophy - pathology | RNA, Guide - biosynthesis | HEK293 Cells | CD24 Antigen - genetics | Myotonic Dystrophy - genetics | Female | Transcription, Genetic | C9orf72 Protein - metabolism | Microsatellite Repeats | Disease Models, Animal | Transduction, Genetic | Down-Regulation | Mice, Transgenic | ran GTP-Binding Protein - metabolism | Myotonic Dystrophy - therapy | Myoblasts - pathology | Chloride Channels - metabolism | Animals | CRISPR-Associated Proteins - metabolism | CRISPR-Cas Systems | Enzyme Activation | HeLa Cells | Genetic Vectors | Genetic Therapy - methods | Enzymes | Genetic transcription | RNA | Health aspects | Analysis | Microbiology | Index Medicus
Journal Article
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 06/2014, Volume 124, Issue 6, pp. 2651 - 2667
Duchenne muscular dystrophy (DMD) is caused by mutations in the gene encoding dystrophin, which results in dysfunctional signaling pathways within muscle.... 
MEDICINE, RESEARCH & EXPERIMENTAL | SKELETAL-MUSCLE | MDX MOUSE | MESSENGER-RNAS | CENTRONUCLEAR MYOPATHY | GLYCOPROTEIN COMPLEX | C2C12 MYOBLAST | TUMOR-SUPPRESSOR | CELL-PROLIFERATION | MYOBLAST FUSION | PROTEIN-KINASE B | Muscular Dystrophy, Animal - genetics | Up-Regulation | Humans | Male | MicroRNAs - metabolism | Muscle, Skeletal - metabolism | Muscle Fibers, Skeletal - metabolism | Muscular Dystrophy, Animal - pathology | Guanine Nucleotide Exchange Factors - metabolism | Base Sequence | Mice, Inbred mdx | Muscular Dystrophy, Animal - metabolism | Proto-Oncogene Proteins c-akt - metabolism | Cell Line | Guanine Nucleotide Exchange Factors - genetics | Signal Transduction | Mice, Inbred C57BL | PTEN Phosphohydrolase - metabolism | Mice, Transgenic | Muscular Dystrophy, Duchenne - pathology | Nerve Tissue Proteins - genetics | Sequence Homology, Nucleic Acid | Nerve Tissue Proteins - metabolism | Carrier Proteins - genetics | Animals | Carrier Proteins - metabolism | Muscle Fibers, Skeletal - pathology | Mice | MicroRNAs - genetics | Muscular Dystrophy, Duchenne - metabolism | Muscle, Skeletal - pathology | Muscular Dystrophy, Duchenne - genetics | MicroRNA | Cellular signal transduction | Genetic aspects | Diagnosis | Properties | Genetic regulation | Muscular dystrophy | Muscular system | Mutation | Rodents | Index Medicus | Abridged Index Medicus
Journal Article