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Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 04/2017, Volume 114, Issue 16, pp. 4213 - 4218
Duchenne muscular dystrophy (DMD) is a lethal genetic disorder caused by an absence of the dystrophin protein in bodywide muscles, including the heart.... 
Cardiac Purkinje fibers | Dystrophic dog model | Peptide-conjugated morpholinos | Duchenne muscular dystrophy | Exon skipping | MUSCLE PATHOLOGY | MULTIDISCIPLINARY SCIENCES | DMD GENE | CARDIOMYOPATHY | BODYWIDE | dystrophic dog model | peptide-conjugated morpholinos | MDX52 MICE | OLIGONUCLEOTIDES | RESCUE | exon skipping | LABORATORY-ANIMALS | cardiac Purkinje fibers | EXPRESSION | EXONS 45-55 | Genetic Therapy | Muscular Dystrophy, Animal - genetics | Exons | Male | Muscle, Skeletal - metabolism | Muscular Dystrophy, Animal - complications | Muscular Dystrophy, Duchenne - complications | Cardiomyopathies - etiology | Cardiomyopathies - therapy | Cell-Penetrating Peptides - pharmacology | Animals | Dogs | Morpholinos - pharmacology | Female | Muscular Dystrophy, Animal - therapy | Muscle, Skeletal - pathology | Muscular Dystrophy, Duchenne - genetics | Muscular Dystrophy, Duchenne - therapy | Dystrophin - metabolism | Disease Models, Animal | Heart | Physiological aspects | Health aspects | Conduction | Intravenous administration | Peptides | Toxicity | Cardiomyopathy | Effects | Muscular dystrophy | Fibers | Oligomers | Nerve conduction | Arginine | Duchenne's muscular dystrophy | Degeneration | Polymers | Heart diseases | Dystrophin | EKG | Cardiac muscle | Abnormalities | Muscles | Skeletal muscle | Purkinje fibers | Myocardium | Dystrophy | Index Medicus | Biological Sciences
Journal Article
PLoS ONE, ISSN 1932-6203, 12/2018, Volume 13, Issue 12, pp. e0208415 - e0208415
Duchenne muscular dystrophy (DMD) is an X-linked muscle disorder characterized by primary muscle degeneration. Patients with DMD reveal progressive muscle... 
ACCELERATION | BIOMARKERS | 6-MINUTE WALK TEST | MRI | LIMB MUSCLES | MULTIDISCIPLINARY SCIENCES | END-POINTS | DUCHENNE MUSCULAR-DYSTROPHY | RELIABILITY | PATHOLOGY | NATURAL-HISTORY | Motor Activity - physiology | Predictive Value of Tests | Prognosis | Muscular Dystrophy, Animal - physiopathology | Magnetic Resonance Imaging - methods | Male | Muscular Dystrophy, Duchenne - pathology | Gait - physiology | Animals | Dog Diseases - physiopathology | Muscular Dystrophy, Duchenne - physiopathology | Accelerometry - veterinary | Muscle, Skeletal - diagnostic imaging | Muscle, Skeletal - physiopathology | Dogs | Magnetic Resonance Imaging - veterinary | Female | Accelerometry - methods | Dog Diseases - diagnosis | Disease Models, Animal | Muscular Dystrophy, Animal - diagnosis | Muscular Dystrophy, Duchenne - diagnosis | Accelerometers | Usage | Magnetic resonance imaging | Duchenne muscular dystrophy | Clinical trials | Models | Research | Health aspects | Neurosciences | Nuclear magnetic resonance--NMR | Gait | Laboratories | Motors | Parameter sensitivity | Muscular dystrophy | Lumbar region | Duchenne's muscular dystrophy | Degeneration | Locomotor activity | Medical research | Evaluation | Muscles | Thorax | Velocity | Neurology | Angular velocity | Dystrophy | Acceleration | Neuromuscular system | Psychiatry | Index Medicus | Nuclear magnetic resonance | NMR
Journal Article
Journal Article
Journal of Personalized Medicine, ISSN 2075-4426, 12/2018, Volume 8, Issue 4, p. 38
Journal Article
Journal Article
CIENCIA RURAL, ISSN 0103-8478, 2017, Volume 47, Issue 10
Golden Retriever muscular dystrophy (GRMD) is the most representative model for studying Duchenne muscular dystrophy (DMD) in humans, owing its phenotypic... 
STEM-CELLS | AGRONOMY | CANINE MODEL | CARDIOMYOPATHY | TRANSDUCTION | GRMD DOGS | GENE | Duchenne muscular dystrophy | MUSCLE FUNCTION | ANIMAL-MODELS | THERAPEUTIC STRATEGIES | animal model | EXPRESSION | dystrophic Golden Retriever
Journal Article
Basic Research in Cardiology, ISSN 0300-8428, 1/2012, Volume 107, Issue 1, pp. 1 - 9
Little is known about the vascular function and expression of endothelial and neuronal nitric oxide synthases (eNOS and nNOS) in Duchenne muscular dystrophy... 
Duchenne muscular dystrophic cardiomyopathy | Endothelial nitric oxide synthase | Neuronal nitric oxide synthase | Medicine & Public Health | Bradykinin | Endothelial dysfunction | Cardiology | CARDIAC & CARDIOVASCULAR SYSTEMS | NITRIC-OXIDE SYNTHASE | HEART-FAILURE | ACE-INHIBITION | DEFICIENT SKELETAL-MUSCLE | DILATED CARDIOMYOPATHY | BLOOD-FLOW | ANGIOTENSIN-CONVERTING ENZYME | ENDOGENOUS BRADYKININ | MYOCARDIAL ISCHEMIA/REPERFUSION | L-ARGININE | Blood Pressure | Ventricular Dysfunction, Left | Endothelium, Vascular - physiopathology | Muscular Dystrophy, Duchenne - enzymology | Nitric Oxide - physiology | Bradykinin - physiology | Animals | Cyclic GMP - metabolism | Muscular Dystrophy, Duchenne - physiopathology | Nitric Oxide Synthase Type I - metabolism | Dogs | Carotid Arteries - enzymology | Nitric Oxide Synthase Type III - metabolism | Disease Models, Animal | Enzymes | Neurons | Vasodilators | Blood vessels | Cyclic guanylic acid | Endothelium | Enzyme inhibitors | Dilatation | Analysis | Duchenne muscular dystrophy | Nitric oxide | Acetylcholine | Index Medicus | Carotid Arteries | Biochemistry, Molecular Biology | Nitric Oxide Synthase Type III | Nitric Oxide | Life Sciences | Nitric Oxide Synthase Type I | Cyclic GMP | Muscular Dystrophy, Duchenne | Endothelium, Vascular | bradykinin | endothelial nitric oxide synthase | neuronal nitric oxide synthase | endothelial dysfunction
Journal Article