Duchenne genetic muscular dystrophies limb girdle. Medical search. Frequent questions

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Anatomy29

Muscle, Skeletal Myoblasts Muscle Fibers, Skeletal Muscles Sarcolemma Limb Buds Shoulder X Chromosome Scapula Extremities Chromosomes, Human, Pair 4 Diaphragm Animal Fins Forelimb Pelvis Clavicle Satellite Cells, Skeletal Muscle Hindlimb Myoblasts, Skeletal Muscle Cells Cells, Cultured Spine Myocardium Lower Extremity Facial Muscles Arm Leg Pectoralis Muscles Neuromuscular Junction

Organisms7

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

Diseases39

Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Animal Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Pelvic Girdle Pain Muscular Dystrophy, Emery-Dreifuss Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Muscular Diseases Distal Myopathies Muscle Weakness Fuchs' Endothelial Dystrophy Retinal Dystrophies Neuromuscular Diseases Myositis, Inclusion Body Disease Models, Animal Pelvic Pain Cardiomyopathies Neuroaxonal Dystrophies Sarcoglycanopathies Walker-Warburg Syndrome Limb Deformities, Congenital Myositis Reflex Sympathetic Dystrophy Syndrome Cardiomyopathy, Dilated Phantom Limb Vitelliform Macular Dystrophy Chromosome Deletion Brachial Plexus Neuritis Scoliosis Intellectual Disability Muscular Atrophy Fibrosis Myotonic Disorders Retinal Degeneration Disease Progression

Chemicals and Drugs41

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment19

Pedigree Heterozygote Detection DNA Mutational Analysis Biopsy Immunohistochemistry Disease Models, Animal Genetic Therapy Muscle Strength Limb Salvage Prenatal Diagnosis Chromosome Mapping Electromyography Polymerase Chain Reaction Electroretinography Genetic Testing Blotting, Western Injections, Intramuscular Fluorescent Antibody Technique Cineradiography

Psychiatry and Psychology2

Phantom Limb Intellectual Disability

Phenomena and Processes35

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

Disciplines and Occupations3

Immunohistochemistry Genetic Counseling Paleontology

Anthropology, Education, Sociology and Social Phenomena2

Fossils Paleontology

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care3

Age of Onset Genetic Counseling Genetic Testing

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

Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Animal Dystrophin Sarcoglycans Mice, Inbred mdx Myotonic Dystrophy Muscular Dystrophy, Facioscapulohumeral Dystroglycans Muscle, Skeletal Pelvic Girdle Pain Caveolin 3 Muscular Dystrophy, Emery-Dreifuss Muscle Proteins Utrophin Calpain Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Muscular Diseases Connectin Creatine Kinase Distal Myopathies Pedigree Myoblasts Muscle Fibers, Skeletal Heterozygote Detection Muscle Weakness Mutation Cytoskeletal Proteins Phenotype Fuchs' Endothelial Dystrophy Mutation, Missense Dystrophin-Associated Proteins Caveolins Muscles Sarcolemma Thymopoietins Limb Buds Membrane Proteins Retinal Dystrophies Collagen Type VI Shoulder Neuromuscular Diseases Exons X Chromosome Scapula Extremities Myositis, Inclusion Body DNA Mutational Analysis Dystrophin-Associated Protein Complex Biopsy Laminin Age of Onset Immunohistochemistry Disease Models, Animal Pelvic Pain Chromosomes, Human, Pair 4 Lamin Type A Cardiomyopathies Regeneration Genetic Linkage Poly(A)-Binding Protein II Genetic Therapy Diaphragm Genes, Recessive Muscle Strength Animal Fins Neuroaxonal Dystrophies Muscle Development Molecular Sequence Data Mice, Inbred C57BL Heterozygote Sarcoglycanopathies Walker-Warburg Syndrome Pregnenediones Forelimb Limb Salvage Pelvis Clavicle Limb Deformities, Congenital Satellite Cells, Skeletal Muscle Myostatin Plectin Dependovirus Myositis Morpholinos Prenatal Diagnosis Chromosome Mapping Consanguinity Genetic Counseling Hindlimb Genes, Dominant Reflex Sympathetic Dystrophy Base Sequence Syndrome Myoblasts, Skeletal Electromyography Cardiomyopathy, Dilated Muscle Cells

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