Patients with diseases like muscular dystrophy. Medical search. Frequent questions

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Anatomy20

Muscle, Skeletal Sarcolemma Myoblasts Muscle Fibers, Skeletal Muscles Cells, Cultured Chromosomes, Human, Pair 4 X Chromosome Diaphragm Satellite Cells, Skeletal Muscle Muscle Cells Myoblasts, Skeletal Nuclear Envelope Myocardium Neuromuscular Junction Fundus Oculi Sarcomeres Cell Line Costameres Myofibrils

Organisms7

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

Diseases43

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 Disease Models, Animal Retinal Dystrophies Inflammation Autoimmune Diseases Neoplasms Arthritis, Rheumatoid Muscular Diseases Neuromuscular Diseases Neuroaxonal Dystrophies Sarcoglycanopathies Walker-Warburg Syndrome Cardiomyopathies Reflex Sympathetic Dystrophy Muscle Weakness Vitelliform Macular Dystrophy Myositis Cardiomyopathy, Dilated Muscular Atrophy Myotonic Disorders Syndrome Retinal Degeneration Retinitis Pigmentosa Distal Myopathies Intellectual Disability Epidermolysis Bullosa Simplex Chromosome Deletion Fibrosis Contracture Scoliosis Corneal Dystrophy, Juvenile Epithelial of Meesmann Disease Progression Myoglobinuria Lipodystrophy

Chemicals and Drugs45

Dystrophin Sarcoglycans Dystroglycans Utrophin Thymopoietins Collagen Type VI Dystrophin-Associated Proteins Creatine Kinase Muscle Proteins Lamin Type A Dystrophin-Associated Protein Complex Laminin Caveolin 3 Poly(A)-Binding Protein II Cytoskeletal Proteins Calpain Plectin Membrane Proteins Connectin Myostatin Lamins Membrane Glycoproteins Creatine Kinase, MM Form Mannosyltransferases N-Acetylglucosaminyltransferases Poly(A)-Binding Protein I Morpholinos Oxepins Integrin alpha Chains Codon, Nonsense Pregnenediones Evans Blue Genetic Markers Caveolins DNA Cardiotoxins RNA, Messenger Glycosyltransferases Nitric Oxide Synthase Type I Oligoribonucleotides, Antisense Collagen Type VIII Oligonucleotides, Antisense Glycerol Kinase DNA Probes MyoD Protein

Analytical, Diagnostic and Therapeutic Techniques and Equipment17

Disease Models, Animal Pedigree Heterozygote Detection Models, Biological Genetic Therapy DNA Mutational Analysis Muscle Strength Chromosome Mapping Immunohistochemistry Electroretinography Polymerase Chain Reaction Biopsy Prenatal Diagnosis Blotting, Western Genetic Testing Fluorescent Antibody Technique Reverse Transcriptase Polymerase Chain Reaction

Psychiatry and Psychology1

Intellectual Disability

Phenomena and Processes39

Phenotype Mutation Chromosomes, Human, Pair 4 Exons Signal Transduction X Chromosome Genetic Linkage Genes, Recessive Consanguinity Regeneration Muscle Development Muscle Strength Heterozygote Base Sequence Genes, Dominant Mutation, Missense Amino Acid Sequence Trinucleotide Repeat Expansion Glycosylation Homozygote Frameshift Mutation Codon, Nonsense Gene Deletion Genetic Markers Gene Expression Regulation Muscle Contraction Sequence Deletion Point Mutation Chromosome Deletion Genetic Vectors Genotype Tandem Repeat Sequences Transgenes Lod Score Haplotypes Alleles Alternative Splicing Gene Expression Founder Effect

Disciplines and Occupations2

Immunohistochemistry Genetic Counseling

Humanities1

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care3

Genetic Counseling Genetic Testing Age of Onset

Geographicals1

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

Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Dystrophin Myotonic Dystrophy Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Facioscapulohumeral Mice, Inbred mdx Muscular Dystrophy, Emery-Dreifuss Sarcoglycans Corneal Dystrophies, Hereditary Dystroglycans Muscular Dystrophy, Oculopharyngeal Utrophin Muscle, Skeletal Phenotype Fuchs' Endothelial Dystrophy Mutation Disease Models, Animal Thymopoietins Retinal Dystrophies Collagen Type VI Mice, Inbred C57BL Pedigree Inflammation India Autoimmune Diseases Dystrophin-Associated Proteins Sarcolemma Heterozygote Detection Models, Biological Neoplasms Creatine Kinase Muscle Proteins Myoblasts Muscle Fibers, Skeletal Muscles Cells, Cultured Chromosomes, Human, Pair 4 Arthritis, Rheumatoid Lamin Type A Exons Dystrophin-Associated Protein Complex Laminin Caveolin 3 Signal Transduction Poly(A)-Binding Protein II Muscular Diseases X Chromosome Neuromuscular Diseases Cytoskeletal Proteins Neuroaxonal Dystrophies Sarcoglycanopathies Walker-Warburg Syndrome Genetic Linkage Calpain Cardiomyopathies Genes, Recessive Plectin Molecular Sequence Data Genetic Therapy Consanguinity Membrane Proteins Connectin Regeneration Muscle Development Reflex Sympathetic Dystrophy Muscle Weakness DNA Mutational Analysis Diaphragm Muscle Strength Heterozygote Vitelliform Macular Dystrophy Chromosome Mapping Base Sequence Myositis Myostatin Genes, Dominant Lamins Satellite Cells, Skeletal Muscle Dependovirus Immunohistochemistry Mice, Transgenic Mutation, Missense Electroretinography Cardiomyopathy, Dilated Muscular Atrophy Amino Acid Sequence Trinucleotide Repeat Expansion Glycosylation Muscle Cells Homozygote Mice, Knockout Myotonic Disorders Myoblasts, Skeletal Membrane Glycoproteins Polymerase Chain Reaction Creatine Kinase, MM Form Mannosyltransferases Biopsy

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