Muscular dystrophy muscle skeletal. Medical search. Frequent questions

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Anatomy52

Muscles Muscle, Skeletal Muscle Fibers, Skeletal Muscle, Smooth Muscle, Smooth, Vascular Myoblasts Sarcolemma Muscle Fibers, Fast-Twitch Chromosomes, Human, Pair 4 Muscle Cells Mitochondria, Muscle Muscle Fibers, Slow-Twitch Satellite Cells, Skeletal Muscle Muscle, Striated X Chromosome Oculomotor Muscles Diaphragm Respiratory Muscles Myocytes, Smooth Muscle Facial Muscles Neck Muscles Masseter Muscle Quadriceps Muscle Muscle Spindles Cells, Cultured Papillary Muscles Myofibrils Myoblasts, Skeletal Abdominal Muscles Neuromuscular Junction Myocardium Hindlimb Sarcomeres Masticatory Muscles Intercostal Muscles Pharyngeal Muscles Pectoralis Muscles Motor Neurons Nuclear Envelope Psoas Muscles Cell Line Shoulder Tendons Temporal Muscle Thigh Costameres Fibroblasts Fundus Oculi Leg Filamins Basement Membrane Sarcoplasmic Reticulum

Organisms10

Mice, Inbred mdx Mice, Inbred C57BL Mice, Transgenic Mice, Knockout Dependovirus Dogs Rabbits Mice, Mutant Strains Chickens Zebrafish

Diseases42

Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Myotonic Dystrophy Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Emery-Dreifuss Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Fuchs' Endothelial Dystrophy Retinal Dystrophies Muscular Diseases Muscle Weakness Neuromuscular Diseases Muscular Atrophy Disease Models, Animal Neuroaxonal Dystrophies Sarcoglycanopathies Walker-Warburg Syndrome Cardiomyopathies Myositis Reflex Sympathetic Dystrophy Vitelliform Macular Dystrophy Cardiomyopathy, Dilated Myotonic Disorders Syndrome Retinal Degeneration Distal Myopathies Retinitis Pigmentosa Fibrosis Intellectual Disability Contracture Hypertrophy Epidermolysis Bullosa Simplex Chromosome Deletion Myoglobinuria Scoliosis Disease Progression Corneal Dystrophy, Juvenile Epithelial of Meesmann Lipodystrophy Muscle Cramp Necrosis

Chemicals and Drugs59

Dystrophin Sarcoglycans Muscle Proteins Dystroglycans Utrophin Thymopoietins Collagen Type VI Creatine Kinase Dystrophin-Associated Proteins Caveolin 3 Lamin Type A Dystrophin-Associated Protein Complex Laminin Poly(A)-Binding Protein II Cytoskeletal Proteins Calpain Myostatin Plectin Membrane Proteins Connectin RNA, Messenger Creatine Kinase, MM Form Lamins MyoD Protein Myosin Heavy Chains Calcium Membrane Glycoproteins Integrin alpha Chains Morpholinos Mannosyltransferases Poly(A)-Binding Protein I N-Acetylglucosaminyltransferases DNA Oxepins Evans Blue Codon, Nonsense Desmin Pregnenediones Cardiotoxins Caveolins Genetic Markers Actins Nitric Oxide Synthase Type I Cobra Cardiotoxin Proteins Protein Isoforms Oligoribonucleotides, Antisense Oligonucleotides, Antisense Myogenin Glycosyltransferases DNA Primers Nuclear Proteins DNA Probes PAX7 Transcription Factor Collagen Type VIII Filamins Glycogen Glycerol Kinase Actinin Receptors, Cholinergic

Analytical, Diagnostic and Therapeutic Techniques and Equipment25

Pedigree Heterozygote Detection Muscle Denervation Disease Models, Animal Electromyography Genetic Therapy Immunohistochemistry DNA Mutational Analysis Muscle Strength Chromosome Mapping Biopsy Blotting, Western Polymerase Chain Reaction Electroretinography Fluorescent Antibody Technique Prenatal Diagnosis Reverse Transcriptase Polymerase Chain Reaction Genetic Testing Injections, Intramuscular Models, Biological Electric Stimulation Microscopy, Electron Gene Transfer Techniques Histocytochemistry Magnetic Resonance Imaging

Psychiatry and Psychology1

Intellectual Disability

Phenomena and Processes50

Muscle Development Muscle Contraction Muscle Fatigue Mutation Exons Chromosomes, Human, Pair 4 Phenotype X Chromosome Regeneration Genetic Linkage Genes, Recessive Muscle Relaxation Consanguinity Isometric Contraction Base Sequence Heterozygote Muscle Strength Genes, Dominant Time Factors Gene Expression Regulation Amino Acid Sequence Mutation, Missense Homozygote Trinucleotide Repeat Expansion Glycosylation Gene Expression Cell Differentiation Frameshift Mutation Biomechanical Phenomena Gene Deletion Codon, Nonsense Genetic Markers Signal Transduction Genetic Vectors Sequence Deletion Aging Transgenes Point Mutation Genotype Chromosome Deletion Alternative Splicing Lod Score Tandem Repeat Sequences Haplotypes Alleles Organ Specificity Physical Exertion Founder Effect Necrosis Protein Binding

Disciplines and Occupations3

Immunohistochemistry Genetic Counseling Histocytochemistry

Humanities1

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care4

Genetic Counseling Genetic Testing Age of Onset Family Health

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

Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Dystrophin Myotonic Dystrophy Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Facioscapulohumeral Mice, Inbred mdx Muscles Muscular Dystrophy, Emery-Dreifuss Muscle, Skeletal Sarcoglycans Muscle Proteins Corneal Dystrophies, Hereditary Dystroglycans Muscular Dystrophy, Oculopharyngeal Muscle Fibers, Skeletal Utrophin Muscle Development Muscle, Smooth Fuchs' Endothelial Dystrophy Muscle Contraction Muscle, Smooth, Vascular Thymopoietins Collagen Type VI Retinal Dystrophies Myoblasts Sarcolemma Pedigree Creatine Kinase Muscular Diseases Dystrophin-Associated Proteins Muscle Weakness Heterozygote Detection Muscle Fatigue Muscle Fibers, Fast-Twitch Muscle Denervation Caveolin 3 Mutation Exons Lamin Type A Dystrophin-Associated Protein Complex Chromosomes, Human, Pair 4 Muscle Cells Laminin Mitochondria, Muscle Neuromuscular Diseases Muscle Fibers, Slow-Twitch Poly(A)-Binding Protein II Satellite Cells, Skeletal Muscle Phenotype Muscular Atrophy Muscle, Striated Disease Models, Animal X Chromosome Oculomotor Muscles Diaphragm Respiratory Muscles Cytoskeletal Proteins Regeneration Calpain Myocytes, Smooth Muscle Neuroaxonal Dystrophies Facial Muscles Genetic Linkage Sarcoglycanopathies Walker-Warburg Syndrome Myostatin Cardiomyopathies Electromyography Neck Muscles Molecular Sequence Data Mice, Inbred C57BL Myositis Masseter Muscle Genes, Recessive Quadriceps Muscle Plectin Muscle Relaxation Muscle Spindles Membrane Proteins Genetic Therapy Cells, Cultured Papillary Muscles Consanguinity Myofibrils Immunohistochemistry Myoblasts, Skeletal Connectin Isometric Contraction DNA Mutational Analysis Base Sequence Reflex Sympathetic Dystrophy Mice, Transgenic Abdominal Muscles Heterozygote Neuromuscular Junction Muscle Strength RNA, Messenger Mice, Knockout

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