Genetic disease called duchenne muscular dystrophy. Medical search. Frequent questions

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Anatomy18

Muscle, Skeletal Sarcolemma Muscle Fibers, Skeletal X Chromosome Muscles Myoblasts Diaphragm Satellite Cells, Skeletal Muscle Myoblasts, Skeletal Muscle Cells Chromosomes, Human, Pair 4 Cells, Cultured Chromosomes, Human, 4-5 Respiratory Muscles Myocardium Hyalin Cell Line Spine

Organisms6

Mice, Inbred mdx Mice, Inbred C57BL Dependovirus Mice, Transgenic Dogs Mice, Knockout

Diseases28

Muscular Dystrophy, Duchenne Muscular Dystrophies Muscular Dystrophy, Animal Muscular Dystrophies, Limb-Girdle Genetic Diseases, Inborn Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Emery-Dreifuss Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Neuromuscular Diseases Disease Models, Animal Fuchs' Endothelial Dystrophy Cardiomyopathies Retinal Dystrophies Muscular Diseases Syndrome Scoliosis Muscle Weakness Chromosome Deletion Genetic Diseases, X-Linked Fibrosis Intellectual Disability Cardiomyopathy, Dilated Neuroaxonal Dystrophies Disease Progression Sarcoglycanopathies Walker-Warburg Syndrome

Chemicals and Drugs35

Dystrophin Utrophin Sarcoglycans Dystroglycans Dystrophin-Associated Proteins Creatine Kinase Dystrophin-Associated Protein Complex Muscle Proteins Pregnenediones Caveolin 3 Morpholinos Cytoskeletal Proteins Thymopoietins Collagen Type VI Laminin Glycerol Kinase Membrane Proteins Myostatin Codon, Nonsense DNA Oligonucleotides, Antisense Nitric Oxide Synthase Type I Integrin alpha Chains Oligoribonucleotides, Antisense Lamin Type A Genetic Markers Poly(A)-Binding Protein II Evans Blue Mazindol RNA, Messenger DNA Probes Phosphodiesterase 5 Inhibitors Calpain Protriptyline Oxadiazoles

Analytical, Diagnostic and Therapeutic Techniques and Equipment25

Heterozygote Detection Pedigree Genetic Therapy Disease Models, Animal Muscle Strength Prenatal Diagnosis Chromosome Mapping Genetic Testing Polymerase Chain Reaction Immunohistochemistry DNA Mutational Analysis Biopsy Gene Transfer Techniques Injections, Intramuscular Blotting, Western Chromosome Banding Neuromuscular Blockade Electroretinography Vital Capacity Reverse Transcriptase Polymerase Chain Reaction Respiratory Therapy Blotting, Southern Inspiratory Capacity Fluorescent Antibody Technique Chest Wall Oscillation

Psychiatry and Psychology5

Projective Techniques Intellectual Disability Stanford-Binet Test Sociology Mesopic Vision

Phenomena and Processes37

X Chromosome Exons Mutation Muscle Strength Regeneration Genetic Linkage Phenotype Heterozygote Genes, Recessive Muscle Development Base Sequence Chromosome Deletion Genetic Vectors Codon, Nonsense Muscle Contraction Chromosomes, Human, Pair 4 Gene Deletion Genetic Markers Polymorphism, Restriction Fragment Length Sequence Deletion Gene Expression Regulation Reading Frames Mosaicism Chromosomes, Human, 4-5 Dependent Ambulation RNA Splicing Vital Capacity Consanguinity Point Mutation Genotype Frameshift Mutation Alleles Transgenes Amino Acid Sequence Mesopic Vision Inspiratory Capacity Gene Expression

Disciplines and Occupations2

Genetic Counseling Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena1

Humanities1

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care2

Genetic Counseling Genetic Testing

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Humanities Information Science Health Care

Muscular Dystrophy, Duchenne Muscular Dystrophies Dystrophin Muscular Dystrophy, Animal Mice, Inbred mdx Utrophin Muscular Dystrophies, Limb-Girdle Genetic Diseases, Inborn Myotonic Dystrophy Muscle, Skeletal Muscular Dystrophy, Facioscapulohumeral Sarcoglycans Heterozygote Detection Dystroglycans Muscular Dystrophy, Emery-Dreifuss Dystrophin-Associated Proteins Sarcolemma Corneal Dystrophies, Hereditary Creatine Kinase Muscle Fibers, Skeletal X Chromosome Exons Muscular Dystrophy, Oculopharyngeal Muscles Pedigree Myoblasts Neuromuscular Diseases Genetic Therapy Dystrophin-Associated Protein Complex Diaphragm Mutation Muscle Proteins Disease Models, Animal Pregnenediones Muscle Strength Fuchs' Endothelial Dystrophy Cardiomyopathies Caveolin 3 Regeneration Genetic Linkage Phenotype Morpholinos Cytoskeletal Proteins Mice, Inbred C57BL Thymopoietins Genetic Counseling Prenatal Diagnosis Dependovirus Heterozygote Retinal Dystrophies Muscular Diseases Collagen Type VI Laminin Molecular Sequence Data Satellite Cells, Skeletal Muscle Chromosome Mapping Glycerol Kinase Genetic Testing Genes, Recessive Muscle Development Syndrome Base Sequence Scoliosis Myoblasts, Skeletal Muscle Weakness Polymerase Chain Reaction Membrane Proteins Chromosome Deletion Genetic Vectors Myostatin Codon, Nonsense Immunohistochemistry DNA DNA Mutational Analysis Muscle Contraction Oligonucleotides, Antisense Muscle Cells Nitric Oxide Synthase Type I Biopsy Integrin alpha Chains Oligoribonucleotides, Antisense Projective Techniques Genetic Diseases, X-Linked Chromosomes, Human, Pair 4 Lamin Type A Fibrosis Mice, Transgenic Gene Transfer Techniques Gene Deletion Genetic Markers Poly(A)-Binding Protein II Evans Blue Mazindol Intellectual Disability Polymorphism, Restriction Fragment Length Dogs Injections, Intramuscular Sequence Deletion Blotting, Western Eugenics

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