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The Journal of Pathology, ISSN 0022-3417, 07/2019
The progress of antisense-based therapies using first generation Morpholino oligonucleotides for Duchenne muscular dystrophy (DMD) is expected to partially... 
Journal Article
SAE technical paper series, Volume 2015-01-1909.
Three-dimensional direct numerical simulations of methane-air turbulent premixed flame propagating in homogenous isotropic turbulence are conducted to... 
Methane | Combustion and combustion processes | Turbulence | Simulation and modeling
eJournal
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 8/2012, Volume 109, Issue 34, pp. 13763 - 13768
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
The Journal of Physical Chemistry C, ISSN 1932-7447, 01/2017, Volume 121, Issue 1, pp. 982 - 982
Journal Article
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
Journal Article
Molecular Therapy, ISSN 1525-0016, 05/2016, Volume 24, pp. S292 - S292
Journal Article
SCIENTIFIC REPORTS, ISSN 2045-2322, 03/2019, Volume 9, Issue 1, pp. 3807 - 11
Duchenne muscular dystrophy (DMD) is a severe muscle disorder characterised by mutations in the DMD gene. Recently, we have completed a phase I study in Japan... 
TRACT | STEM-CELLS | GENE | MYOD | MULTIDISCIPLINARY SCIENCES | ABILITY | GENERATION | DIFFERENTIATION | MUTATIONS | EXPRESSION | MYOGENIN | Urine | Myogenin | Exons | Clinical trials | Antisense | Drug delivery | Drug development | Patients | Muscular dystrophy | Duchenne's muscular dystrophy | Histone methyltransferase | Dystrophy | Dystrophin
Journal Article
Molecular Therapy, ISSN 1525-0016, 11/2017, Volume 25, Issue 11, pp. 2561 - 2572
Duchenne muscular dystrophy (DMD), the most common lethal genetic disorder, is caused by mutations in the ( ) gene. Exon skipping is a therapeutic approach... 
mdx52 mice | Becker muscular dystrophy | Exondys 51 | eteplirsen | exon skipping | Duchenne muscular dystrophy | clinical trial candidate screening | BMD | antisense morpholino | drisapersen | machine learning | hDMD/Dmd-null mice | MEDICINE, RESEARCH & EXPERIMENTAL | DIAGNOSIS | DESIGN | EFFICACY | DMD GENE | RESTORATION | PHASE-2 | OLIGONUCLEOTIDES | THERAPY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | MICE | ETEPLIRSEN | Exons | Humans | Oligonucleotides, Antisense - metabolism | Male | Muscle, Skeletal - metabolism | Reading Frames | Recovery of Function | RNA Splicing | Female | Muscular Dystrophy, Duchenne - therapy | Dystrophin - metabolism | Disease Models, Animal | Gene Expression | Morpholinos - genetics | Mice, Transgenic | Muscular Dystrophy, Duchenne - pathology | Morpholinos - metabolism | Animals | Oligonucleotides, Antisense - genetics | Dystrophin - genetics | Mice | Muscular Dystrophy, Duchenne - metabolism | Muscle, Skeletal - pathology | Muscular Dystrophy, Duchenne - genetics | Mutation | Genetic Therapy - methods | Performance evaluation | Medical research | Statistical analysis | Splicing | Antisense oligonucleotides | Muscular dystrophy | Proteins | Musculoskeletal system | Protein folding | Efficiency | Exon skipping | Duchenne's muscular dystrophy | Protein expression | Muscle function | Dystrophy | Dystrophin | Evacuations & rescues | Index Medicus | hDMD | Dmd-null mice | Original
Journal Article