Diseases like duchenne muscular dystrophy and parkinson s. Medical search. Frequent questions

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Anatomy17

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

Organisms6

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

Diseases32

Muscular Dystrophy, Duchenne Muscular Dystrophies Muscular Dystrophy, Animal Parkinson Disease Muscular Dystrophies, Limb-Girdle Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Emery-Dreifuss Corneal Dystrophies, Hereditary Disease Models, Animal Muscular Dystrophy, Oculopharyngeal Neuromuscular Diseases Cardiomyopathies Fuchs' Endothelial Dystrophy Retinal Dystrophies Muscular Diseases Inflammation Autoimmune Diseases Scoliosis Muscle Weakness Chromosome Deletion Neoplasms Syndrome Arthritis, Rheumatoid Fibrosis Cardiomyopathy, Dilated Disease Progression Parkinsonian Disorders Intellectual Disability Neuroaxonal Dystrophies Sarcoglycanopathies Walker-Warburg Syndrome

Chemicals and Drugs38

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 alpha-Synuclein Myostatin Membrane Proteins Oligonucleotides, Antisense Nitric Oxide Synthase Type I Integrin alpha Chains Oligoribonucleotides, Antisense Lamin Type A Poly(A)-Binding Protein II Evans Blue Mazindol Antiparkinson Agents DNA Genetic Markers Codon, Nonsense DNA Probes RNA, Messenger Phosphodiesterase 5 Inhibitors Calpain Protriptyline Oxadiazoles Membrane Glycoproteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment25

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

Psychiatry and Psychology5

Projective Techniques Stanford-Binet Test Sociology Intellectual Disability Mesopic Vision

Phenomena and Processes33

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

Disciplines and Occupations2

Genetic Counseling Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena1

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care2

Genetic Counseling Genetic Testing

Geographicals1

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 Information Science Health Care Geographicals

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

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