Muscular dystrophies 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 Nuclear Envelope Neuromuscular Junction Facial Muscles Shoulder Fundus Oculi Sarcomeres

Organisms7

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

Diseases37

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

Chemicals and Drugs44

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment19

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

Psychiatry and Psychology1

Intellectual Disability

Phenomena and Processes40

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

Disciplines and Occupations2

Genetic Counseling Immunohistochemistry

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 Information Science Health Care

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

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