Duchenne Muscular Dystrophy

Micro-dystrophin cDNA ameliorates dystrophic phenotypes when introduced into mdx mice as a transgene

Skeletal muscle biology / Fluorescence Microscopy / Gene Therapy / Immunohistochemistry / Western blotting / Transgenic Mice / Humans / Mice / Animals / Adeno-associated virus / Biochemical / Duchenne Muscular Dystrophy / Creatine Kinase / Phenotype / Skeletal Muscle / Time Factors / Dystrophin / Biochemistry and cell biology / Gene Transfer / Transgenic Mice / Humans / Mice / Animals / Adeno-associated virus / Biochemical / Duchenne Muscular Dystrophy / Creatine Kinase / Phenotype / Skeletal Muscle / Time Factors / Dystrophin / Biochemistry and cell biology / Gene Transfer

Adeno-associated virus vector-mediated gene transfer into dystrophin-deficient skeletal muscles evokes enhanced immune response against the transgene product

Immune response / Skeletal muscle biology / Gene Therapy / Biological Sciences / Mice / Female / Animals / Gene transfer techniques / Male / Immunosuppression / Adeno-associated virus / Duchenne Muscular Dystrophy / Skeletal Muscle / Degeneration / Dystrophin / Gene Transfer / Female / Animals / Gene transfer techniques / Male / Immunosuppression / Adeno-associated virus / Duchenne Muscular Dystrophy / Skeletal Muscle / Degeneration / Dystrophin / Gene Transfer

Novel Long Noncoding RNAs (lncRNAs) in Myogenesis: a miR-31 Overlapping lncRNA Transcript Controls Myoblast Differentiation

Long Noncoding Rna / Transcriptome / Biological Sciences / Cell Differentiation / Molecular and cellular biology / Humans / Smooth muscle / Mice / Animals / Biological evolution / Duchenne Muscular Dystrophy / microRNAs / Muscle development / Cell Proliferation / Gene Expression Regulation / Gene expression profiling / Myoblasts / Humans / Smooth muscle / Mice / Animals / Biological evolution / Duchenne Muscular Dystrophy / microRNAs / Muscle development / Cell Proliferation / Gene Expression Regulation / Gene expression profiling / Myoblasts

Distrofia muscular de Duchenne: análise eletrocardiográfica de 131 pacientes

Electrocardiography / Humans / Child / Male / Duchenne Muscular Dystrophy / Age Factors / Reference Values / Arquivos brasileiros / Heart Diseases / Age Factors / Reference Values / Arquivos brasileiros / Heart Diseases

Recomendaciones de buenas prácticas para el diagnóstico genético de la distrofia miotónica

Benchmarking / Software Design / Pregnancy / Humans / Genetic Testing / Mutation / Haplotypes / Female / Male / Polymerase Chain Reaction / Myotonic Dystrophy / Duchenne Muscular Dystrophy / Preimplantation genetic diagnosis / RNA-binding proteins / Prenatal Diagnosis / Molecular Diagnostic Techniques / Dystrophin / Medicina Clinica / Early Diagnosis / Genetic Markers / Mutation / Haplotypes / Female / Male / Polymerase Chain Reaction / Myotonic Dystrophy / Duchenne Muscular Dystrophy / Preimplantation genetic diagnosis / RNA-binding proteins / Prenatal Diagnosis / Molecular Diagnostic Techniques / Dystrophin / Medicina Clinica / Early Diagnosis / Genetic Markers

Recomendaciones de buenas prácticas para el diagnóstico genético de la distrofia miotónica

Benchmarking / Software Design / Pregnancy / Humans / Genetic Testing / Mutation / Haplotypes / Female / Male / Polymerase Chain Reaction / Myotonic Dystrophy / Duchenne Muscular Dystrophy / Preimplantation genetic diagnosis / RNA-binding proteins / Prenatal Diagnosis / Molecular Diagnostic Techniques / Dystrophin / Medicina Clinica / Early Diagnosis / Genetic Markers / Mutation / Haplotypes / Female / Male / Polymerase Chain Reaction / Myotonic Dystrophy / Duchenne Muscular Dystrophy / Preimplantation genetic diagnosis / RNA-binding proteins / Prenatal Diagnosis / Molecular Diagnostic Techniques / Dystrophin / Medicina Clinica / Early Diagnosis / Genetic Markers

Exon-skipping antisense oligonucleotides to correct missplicing in neurogenetic diseases

Humans / Mutation / Blood brain barrier / Animals / Drug Delivery Systems / Duchenne Muscular Dystrophy / Frontotemporal Dementia / Nervous System Diseases / Ataxia Telangiectasia / Duchenne Muscular Dystrophy / Frontotemporal Dementia / Nervous System Diseases / Ataxia Telangiectasia

Distrofia muscular de Duchenne: análise eletrocardiográfica de 131 pacientes

Electrocardiography / Humans / Child / Male / Duchenne Muscular Dystrophy / Age Factors / Reference Values / Arquivos brasileiros / Heart Diseases / Age Factors / Reference Values / Arquivos brasileiros / Heart Diseases

Magnetic resonance spectroscopy evidence of abnormal cardiac energetics in Xp21 muscular dystrophy

Signal Processing / Magnetic Resonance Spectroscopy / Energy Metabolism / Phosphorus / Cardiac Hypertrophy / Humans / Left Ventricular Assist Device / Muscular Dystrophy / Female / Male / Duchenne Muscular Dystrophy / Dilated cardiomyopathy / Middle Aged / Skeletal Muscle / Adult / Myocardium / Public health systems and services research / Cardiomyopathies / Left Ventricular Function / Chemical Shift Imaging / Adenosine Triphosphate / The American / Becker Muscular Dystrophy (BMD) / Phosphocreatine / Humans / Left Ventricular Assist Device / Muscular Dystrophy / Female / Male / Duchenne Muscular Dystrophy / Dilated cardiomyopathy / Middle Aged / Skeletal Muscle / Adult / Myocardium / Public health systems and services research / Cardiomyopathies / Left Ventricular Function / Chemical Shift Imaging / Adenosine Triphosphate / The American / Becker Muscular Dystrophy (BMD) / Phosphocreatine

[Diagnosis and treatment with steroids for patients with Duchenne muscular dystrophy: experience and recommendations for Mexico. Administración del Patrimonio de la Beneficencia Pública. Asociación de Distrofia Muscular de Occidente]

Obesity / Quality of life / Mexico / Respiratory therapy / Humans / Hyperglycemia / Male / Immunosuppression / Differential Diagnosis / Incidence / Caregivers / Duchenne Muscular Dystrophy / Patient Care Team / MEXICO / Molecular Diagnostic Techniques / Dystrophin / Hyperglycemia / Male / Immunosuppression / Differential Diagnosis / Incidence / Caregivers / Duchenne Muscular Dystrophy / Patient Care Team / MEXICO / Molecular Diagnostic Techniques / Dystrophin

Talin, Vinculin and Nestin Expression in Orofacial Muscles of Dystrophin Deficient mdx Mice

Microbiology / Immunology / Regeneration / Humans / Mutation / Mice / Animals / Duchenne Muscular Dystrophy / Dystrophin / Vinculin / Mice / Animals / Duchenne Muscular Dystrophy / Dystrophin / Vinculin

Ochre Suppressor Transfer Rna Restored Dystrophin Expression in MDX Mice

Genetics / Life Sciences / Gene expression / Mice / Animals / Animal Model / Duchenne Muscular Dystrophy / Genetic Disorder / Plasmid DNA / Direct Injection / Biochemistry and cell biology / Animal Model / Duchenne Muscular Dystrophy / Genetic Disorder / Plasmid DNA / Direct Injection / Biochemistry and cell biology

Muscle pathology in dysferlin deficiency

Cognitive Science / Skeletal muscle biology / Membrane Proteins / Immunohistochemistry / Adolescent / Biopsy / Humans / Child / Female / Muscular Dystrophies / Male / Infant / Duchenne Muscular Dystrophy / Clinical Sciences / Middle Aged / Adult / Myositis / Neurosciences / Immunoblotting / Biopsy / Humans / Child / Female / Muscular Dystrophies / Male / Infant / Duchenne Muscular Dystrophy / Clinical Sciences / Middle Aged / Adult / Myositis / Neurosciences / Immunoblotting

PNA-peptide conjugates as intracellular gene control agents

Humans / Mice / Animals / Peptide Nucleic Acids / Duchenne Muscular Dystrophy / microRNAs / HeLa cells / microRNAs / HeLa cells

PNA-peptide conjugates as intracellular gene control agents

Humans / Mice / Animals / Peptide Nucleic Acids / Duchenne Muscular Dystrophy / microRNAs / HeLa cells / microRNAs / HeLa cells

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