People muscular dystrophy duchenne. Medical search. Frequent questions

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Anatomy19

Muscle, Skeletal Sarcolemma Muscle Fibers, Skeletal Muscles Myoblasts X Chromosome Chromosomes, Human, Pair 4 Diaphragm Satellite Cells, Skeletal Muscle Myoblasts, Skeletal Muscle Cells Myocardium Cells, Cultured Facial Muscles Neuromuscular Junction Shoulder Nuclear Envelope Respiratory Muscles Cell Line

Organisms7

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

Diseases38

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

Chemicals and Drugs46

Dystrophin Utrophin Sarcoglycans Dystroglycans Dystrophin-Associated Proteins Thymopoietins Creatine Kinase Collagen Type VI Muscle Proteins Dystrophin-Associated Protein Complex Caveolin 3 Laminin Lamin Type A Cytoskeletal Proteins Poly(A)-Binding Protein II Calpain Pregnenediones Membrane Proteins Plectin Myostatin Morpholinos Connectin Integrin alpha Chains Evans Blue Glycerol Kinase Lamins Codon, Nonsense Membrane Glycoproteins Genetic Markers Nitric Oxide Synthase Type I DNA Oligoribonucleotides, Antisense Oligonucleotides, Antisense Creatine Kinase, MM Form Mannosyltransferases DNA Probes RNA, Messenger N-Acetylglucosaminyltransferases Poly(A)-Binding Protein I Oxepins Deoxyribonuclease HindIII Mazindol Caveolins MyoD Protein Cardiotoxins Phosphodiesterase 5 Inhibitors

Analytical, Diagnostic and Therapeutic Techniques and Equipment22

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

Psychiatry and Psychology3

Intellectual Disability Projective Techniques Stanford-Binet Test

Phenomena and Processes41

Exons X Chromosome Mutation Chromosomes, Human, Pair 4 Phenotype Genetic Linkage Muscle Strength Regeneration Genes, Recessive Heterozygote Muscle Development Consanguinity Base Sequence Chromosome Deletion Genes, Dominant Muscle Contraction Gene Deletion Frameshift Mutation Codon, Nonsense Genetic Markers Sequence Deletion Mutation, Missense Genetic Vectors Trinucleotide Repeat Expansion Homozygote Gene Expression Regulation Glycosylation Amino Acid Sequence Polymorphism, Restriction Fragment Length Mosaicism Point Mutation Reading Frames Genotype Time Factors Transgenes Haplotypes Alleles Gene Expression RNA Splicing Alternative Splicing Necrosis

Disciplines and Occupations2

Genetic Counseling Immunohistochemistry

Humanities1

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care3

Genetic Counseling Genetic Testing Age of Onset

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

Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Dystrophin Mice, Inbred mdx Muscular Dystrophies, Limb-Girdle Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Emery-Dreifuss Utrophin Sarcoglycans Dystroglycans Corneal Dystrophies, Hereditary Muscle, Skeletal Muscular Dystrophy, Oculopharyngeal Heterozygote Detection Fuchs' Endothelial Dystrophy Dystrophin-Associated Proteins Sarcolemma Pedigree Thymopoietins Creatine Kinase Muscle Fibers, Skeletal Retinal Dystrophies Collagen Type VI Muscles Exons Myoblasts X Chromosome Muscle Proteins Dystrophin-Associated Protein Complex Neuromuscular Diseases Caveolin 3 Mutation Laminin Muscular Diseases Disease Models, Animal Chromosomes, Human, Pair 4 Lamin Type A Cytoskeletal Proteins Cardiomyopathies Phenotype Genetic Linkage Poly(A)-Binding Protein II Genetic Therapy Diaphragm Muscle Strength Regeneration Neuroaxonal Dystrophies Sarcoglycanopathies Genes, Recessive Walker-Warburg Syndrome Heterozygote Muscle Development Calpain Muscle Weakness Mice, Inbred C57BL Pregnenediones Membrane Proteins Molecular Sequence Data Plectin Satellite Cells, Skeletal Muscle Myostatin Dependovirus Morpholinos DNA Mutational Analysis Myositis Prenatal Diagnosis Genetic Counseling Chromosome Mapping Consanguinity Connectin Reflex Sympathetic Dystrophy Immunohistochemistry Base Sequence Myoblasts, Skeletal Cardiomyopathy, Dilated Syndrome Polymerase Chain Reaction Muscle Cells Biopsy Vitelliform Macular Dystrophy Mice, Transgenic Chromosome Deletion Genetic Testing Electroretinography Intellectual Disability Integrin alpha Chains Genes, Dominant Evans Blue Glycerol Kinase Muscle Contraction Gene Deletion Lamins Frameshift Mutation Codon, Nonsense Mice, Knockout Scoliosis Blotting, Western Membrane Glycoproteins

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