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Human Molecular Genetics, ISSN 0964-6906, 2/2009, Volume 18, Issue 4, pp. 607 - 620
Journal Article
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 1/2009, Volume 184, Issue 1, pp. 31 - 44
Journal Article
Journal Article
Clinical Genetics, ISSN 0009-9163, 08/2016, Volume 90, Issue 2, pp. 171 - 176
Journal Article
Journal Article
Circulation, ISSN 0009-7322, 08/2017, Volume 136, Issue 13, pp. e200 - e231
For many neuromuscular diseases (NMDs), cardiac disease represents a major cause of morbidity and mortality. The management of cardiac disease in NMDs is made... 
Neuromuscular disease | Pediatrics | Cardiomyopathy | Muscular dystrophy | AHA Scientific Statements | CARDIAC & CARDIOVASCULAR SYSTEMS | CARDIOVASCULAR MAGNETIC-RESONANCE | MECHANICAL CIRCULATORY SUPPORT | neuromuscular disease | CONVERTING ENZYME-INHIBITORS | LUNG TRANSPLANTATION GUIDELINES | LEFT-VENTRICULAR NONCOMPACTION | muscular dystrophy | pediatrics | CHEYNE-STOKES RESPIRATION | LAMIN A/C GENE | PERIPHERAL VASCULAR DISEASE | DUCHENNE MUSCULAR-DYSTROPHY | MYOCARDIAL DELAYED ENHANCEMENT | cardiomyopathy | CARDIOSELECTIVE BETA-BLOCKERS | Myotonic Dystrophy - metabolism | Barth Syndrome - metabolism | Friedreich Ataxia - pathology | Myotonic Dystrophy - diagnosis | United States | Humans | Myopathies, Structural, Congenital - genetics | Neuromuscular Diseases - pathology | Barth Syndrome - pathology | Myotonic Dystrophy - pathology | Muscular Dystrophy, Emery-Dreifuss - diagnosis | Cardiomyopathies - diagnosis | Neuromuscular Diseases - diagnosis | Muscular Dystrophies, Limb-Girdle - pathology | Friedreich Ataxia - metabolism | Muscular Dystrophies, Limb-Girdle - diagnosis | Muscular Diseases - metabolism | Risk Factors | Friedreich Ataxia - diagnosis | Muscular Dystrophy, Emery-Dreifuss - pathology | Cardiomyopathies - pathology | Muscular Dystrophy, Duchenne - pathology | Muscular Diseases - pathology | Barth Syndrome - diagnosis | American Heart Association | Muscular Diseases - diagnosis | Muscular Dystrophy, Emery-Dreifuss - metabolism | Muscular Dystrophies, Limb-Girdle - metabolism | Barth Syndrome - genetics | Neuromuscular Diseases - complications | Myopathies, Structural, Congenital - pathology | Cardiomyopathies - complications | Myopathies, Structural, Congenital - diagnosis | Muscular Dystrophy, Duchenne - metabolism | Myopathies, Structural, Congenital - metabolism | Muscular Dystrophy, Duchenne - diagnosis | Index Medicus | Abridged Index Medicus
Journal Article
Cellular Physiology and Biochemistry, ISSN 1015-8987, 06/2017, Volume 42, Issue 1, pp. 169 - 184
Background: Ankrd2 is a stress responsive protein mainly expressed in muscle cells. Upon the application of oxidative stress, Ankrd2 translocates into the... 
Prelamin A | Oxidative stress | Ankrd2 (Ankyrin Repeat Domain 2) | Human muscle cells | EDMD2 (Emery-Dreifuss Muscular Dystrophy 2) | Lamin A/C | PHYSIOLOGY | DNA-DAMAGE | ROS GENERATION | FAMILY | CELL BIOLOGY | SKELETAL-MUSCLE | MYOGENIC DIFFERENTIATION | ANKYRIN-REPEATED PROTEIN | PRELAMIN-A | SENESCENCE | STRIATED-MUSCLE | REPEAT PROTEIN | Immunoprecipitation | Reactive Oxygen Species - metabolism | Humans | Lamin Type A - chemistry | Muscle, Skeletal - metabolism | Muscle, Skeletal - cytology | Myoblasts - drug effects | Myoblasts - metabolism | Cell Nucleus - metabolism | Muscle, Skeletal - drug effects | HEK293 Cells | Muscle Proteins - metabolism | Myoblasts - cytology | Plasmids - genetics | Nuclear Proteins - genetics | Repressor Proteins - metabolism | Hydrogen Peroxide - toxicity | Cell Survival - drug effects | Muscular Dystrophy, Emery-Dreifuss - genetics | Protein Prenylation - drug effects | Repressor Proteins - chemistry | Cells, Cultured | Muscular Dystrophy, Emery-Dreifuss - pathology | Repressor Proteins - genetics | Nuclear Proteins - metabolism | Lamin Type A - metabolism | Nuclear Proteins - chemistry | Plasmids - metabolism | Muscle Proteins - genetics | Muscular Dystrophy, Emery-Dreifuss - metabolism | Lamin Type A - genetics | Protein Binding | Muscle Proteins - chemistry | Oxidative Stress - drug effects | Microscopy, Fluorescence | Senescence | Smooth muscle | Gene expression | Muscular dystrophy | Proteins | Musculoskeletal system | Rodents | Cell cycle | Mutation | Localization | Deoxyribonucleic acid--DNA | Apoptosis | Index Medicus
Journal Article
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 2014, Volume 25, Issue 2, pp. 127 - 136
Journal Article