Caused by mutations muscular dystrophies. Medical search. Frequent questions

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Anatomy26

Muscle, Skeletal Sarcolemma Myoblasts Muscle Fibers, Skeletal Muscles X Chromosome Chromosomes, Human, Pair 4 Diaphragm Cell Line Satellite Cells, Skeletal Muscle Cells, Cultured Muscle Cells Myoblasts, Skeletal Nuclear Envelope COS Cells Fibroblasts Myocardium Fundus Oculi Sarcomeres Cell Nucleus Neuromuscular Junction Myofibrils Filamins Cornea Chromosomes, Human, Pair 19 Costameres

Organisms11

Mice, Inbred mdx Mice, Inbred C57BL Mice, Transgenic Mice, Knockout Mice, Mutant Strains Dependovirus Escherichia coli Zebrafish Dogs Cricetinae Saccharomyces cerevisiae

Diseases47

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 Disease Models, Animal Neuromuscular Diseases Neuroaxonal Dystrophies Walker-Warburg Syndrome Cardiomyopathies Sarcoglycanopathies Syndrome Muscle Weakness Reflex Sympathetic Dystrophy Vitelliform Macular Dystrophy Retinitis Pigmentosa Myositis Retinal Degeneration Cardiomyopathy, Dilated Intellectual Disability Chromosome Deletion Myotonic Disorders Muscular Atrophy Genetic Diseases, X-Linked Genetic Predisposition to Disease Epidermolysis Bullosa Simplex Distal Myopathies Abnormalities, Multiple Disease Progression Eye Abnormalities Contracture Fibrosis Lipodystrophy Corneal Dystrophy, Juvenile Epithelial of Meesmann Scoliosis Myoglobinuria Macular Degeneration Genetic Diseases, Inborn Myotonia Congenita Eye Diseases, Hereditary

Chemicals and Drugs68

Dystrophin Sarcoglycans Dystroglycans Utrophin Thymopoietins Collagen Type VI Dystrophin-Associated Proteins Muscle Proteins Creatine Kinase Lamin Type A Laminin Caveolin 3 Dystrophin-Associated Protein Complex Poly(A)-Binding Protein II Cytoskeletal Proteins Membrane Proteins Codon, Nonsense Calpain Plectin Connectin DNA DNA Primers Myostatin RNA, Messenger Lamins Genetic Markers Membrane Glycoproteins Nuclear Proteins N-Acetylglucosaminyltransferases Eye Proteins Mannosyltransferases Morpholinos Mutant Proteins Creatine Kinase, MM Form Codon Poly(A)-Binding Protein I Carrier Proteins Transcription Factors DNA-Binding Proteins Integrin alpha Chains Oxepins Proteins Pregnenediones Evans Blue Caveolins Codon, Terminator DNA Probes Glycosyltransferases RNA Splice Sites DNA, Complementary Cardiotoxins Nitric Oxide Synthase Type I Oligoribonucleotides, Antisense Homeodomain Proteins Collagen Type VIII Extracellular Matrix Proteins Oligonucleotides, Antisense Recombinant Fusion Proteins Recombinant Proteins Filamins Glycerol Kinase Protein Isoforms RNA-Binding Proteins Intermediate Filament Proteins Protein-Serine-Threonine Kinases MyoD Protein Nerve Tissue Proteins Bacterial Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment33

Pedigree Heterozygote Detection DNA Mutational Analysis Polymerase Chain Reaction Disease Models, Animal Chromosome Mapping Genetic Testing Amino Acid Substitution Genetic Therapy Sequence Analysis, DNA Immunohistochemistry Muscle Strength Mutagenesis, Site-Directed Electroretinography Blotting, Western Biopsy Models, Molecular Cloning, Molecular Reverse Transcriptase Polymerase Chain Reaction Models, Genetic Prenatal Diagnosis Transfection Fluorescent Antibody Technique Sequence Alignment Blotting, Southern Genetic Complementation Test Models, Biological Mutagenesis, Insertional Crosses, Genetic Gene Targeting Restriction Mapping Gene Transfer Techniques Keratoplasty, Penetrating

Psychiatry and Psychology2

Intellectual Disability Family

Phenomena and Processes76

Point Mutation Mutation, Missense Mutation Frameshift Mutation Exons Heterozygote Phenotype Germ-Line Mutation Genes, Recessive Base Sequence X Chromosome Genetic Linkage Chromosomes, Human, Pair 4 Homozygote Consanguinity Genes, Dominant Codon, Nonsense Amino Acid Sequence Alleles Polymorphism, Single-Stranded Conformational Genotype Amino Acid Substitution Mutation Rate Sequence Deletion Gene Deletion Muscle Development Regeneration Founder Effect Muscle Strength Protein Structure, Tertiary Mutagenesis Genetic Markers Glycosylation Sequence Homology, Amino Acid Gene Expression Regulation Protein Binding Trinucleotide Repeat Expansion Chromosome Deletion Polymorphism, Restriction Fragment Length Introns Polymorphism, Genetic Binding Sites Gene Expression Codon RNA Splicing Mosaicism Genetic Vectors Genetic Predisposition to Disease Microsatellite Repeats Exome Alternative Splicing Transfection Lod Score Signal Transduction Tandem Repeat Sequences Transcription, Genetic Transgenes Suppression, Genetic Recombination, Genetic Muscle Contraction Plasmids Time Factors INDEL Mutation Promoter Regions, Genetic Codon, Terminator Genetic Heterogeneity RNA Splice Sites Repetitive Sequences, Nucleic Acid Genetic Variation Mutagenesis, Insertional Genes Gene Frequency Genes, p53 Cell Differentiation Haplotypes Chromosomes, Human, Pair 19

Disciplines and Occupations2

Immunohistochemistry Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

Humanities1

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Health Care4

Genetic Testing Age of Onset Family Health Genetic Counseling

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 Muscular Dystrophy, Emery-Dreifuss Sarcoglycans Point Mutation Mutation, Missense Corneal Dystrophies, Hereditary Dystroglycans Mutation Muscular Dystrophy, Oculopharyngeal Utrophin Muscle, Skeletal Pedigree Fuchs' Endothelial Dystrophy Frameshift Mutation Exons Thymopoietins Retinal Dystrophies Collagen Type VI Heterozygote Detection Dystrophin-Associated Proteins Muscle Proteins Sarcolemma Heterozygote Phenotype Creatine Kinase DNA Mutational Analysis Myoblasts Muscle Fibers, Skeletal Germ-Line Mutation Genes, Recessive Base Sequence Molecular Sequence Data Muscles Lamin Type A X Chromosome Genetic Linkage Laminin Chromosomes, Human, Pair 4 Muscular Diseases Caveolin 3 Dystrophin-Associated Protein Complex Polymerase Chain Reaction Poly(A)-Binding Protein II Cytoskeletal Proteins Homozygote Consanguinity Disease Models, Animal Genes, Dominant Chromosome Mapping Membrane Proteins Codon, Nonsense Neuromuscular Diseases Amino Acid Sequence Alleles Neuroaxonal Dystrophies Polymorphism, Single-Stranded Conformational Walker-Warburg Syndrome Genotype Calpain Cardiomyopathies Genetic Testing Sarcoglycanopathies Amino Acid Substitution Mutation Rate Sequence Deletion Syndrome Plectin Gene Deletion Genetic Therapy Mice, Inbred C57BL Connectin Muscle Development Muscle Weakness Regeneration Sequence Analysis, DNA DNA Mice, Transgenic DNA Primers Reflex Sympathetic Dystrophy Vitelliform Macular Dystrophy Immunohistochemistry Diaphragm Cell Line Founder Effect Muscle Strength Protein Structure, Tertiary Retinitis Pigmentosa Mutagenesis, Site-Directed Age of Onset Electroretinography Myostatin RNA, Messenger Myositis

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