Pathogenesis genetic autosomal recessive form muscular dystrophies. Medical search. Frequent questions

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Anatomy27

Muscle, Skeletal X Chromosome Sarcolemma Chromosomes, Human, Pair 4 Muscles Myoblasts Muscle Fibers, Skeletal Chromosomes, Human, Pair 2 Cells, Cultured Diaphragm Fundus Oculi Mitochondria Chromosomes, Human, Pair 1 Cell Line Chromosomes, Human, Pair 19 Fibroblasts Satellite Cells, Skeletal Muscle Chromosomes, Human, Pair 5 Muscle Cells Brain Myoblasts, Skeletal Chromosomes, Human, Pair 6 Skin Chromosomes, Human, Pair 10 Myocardium Photoreceptor Cells, Vertebrate Nuclear Envelope

Organisms7

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

Diseases90

Muscular Dystrophies Muscular Dystrophy, Duchenne Muscular Dystrophy, Animal Muscular Dystrophies, Limb-Girdle Myotonic Dystrophy Granulomatous Disease, Chronic Muscular Dystrophy, Facioscapulohumeral Spastic Paraplegia, Hereditary Syndrome Muscular Dystrophy, Emery-Dreifuss Immunologic Deficiency Syndromes Corneal Dystrophies, Hereditary Muscular Dystrophy, Oculopharyngeal Parkinson Disease Arthrogryposis Dysostoses Abnormalities, Multiple Fuchs' Endothelial Dystrophy Retinal Dystrophies Polycystic Kidney, Autosomal Recessive Hearing Loss, Sensorineural Ectodermal Dysplasia Deafness Retinitis Pigmentosa Charcot-Marie-Tooth Disease Disease Models, Animal Osteogenesis Imperfecta Muscular Diseases Intellectual Disability Neuromuscular Diseases Neuroaxonal Dystrophies Microcephaly Walker-Warburg Syndrome Hypotrichosis Cardiomyopathies Ichthyosis Retinal Degeneration Vitelliform Macular Dystrophy Sarcoglycanopathies Ichthyosiform Erythroderma, Congenital Muscle Weakness Eye Diseases, Hereditary Nails, Malformed Chromosome Disorders Reflex Sympathetic Dystrophy Ichthyosis, Lamellar Dwarfism Cerebellar Ataxia Myositis Muscular Atrophy Osteochondrodysplasias Cardiomyopathy, Dilated Eye Abnormalities Genetic Predisposition to Disease Genetic Diseases, Inborn Muscular Atrophy, Spinal Myotonic Disorders Bone Diseases, Developmental Distal Myopathies Osteopetrosis Disease Progression Metabolism, Inborn Errors Epidermolysis Bullosa Myotonia Congenita Chromosome Deletion Genetic Diseases, X-Linked Albinism, Oculocutaneous Contracture Microphthalmos Night Blindness Macular Degeneration Foot Deformities, Congenital Muscle Hypotonia Friedreich Ataxia Kidney Diseases, Cystic Color Vision Defects Retinal Diseases Hair Diseases Cystinosis Cutis Laxa Lipodystrophy Hearing Loss Leber Congenital Amaurosis Rare Diseases Fibrosis Amino Acid Metabolism, Inborn Errors Optic Atrophy Tooth Abnormalities Polycystic Kidney Diseases Epidermolysis Bullosa Simplex

Chemicals and Drugs48

Dystrophin Sarcoglycans Dystroglycans Genetic Markers Utrophin Codon, Nonsense Thymopoietins Collagen Type VI Collagen Type XI Muscle Proteins Dystrophin-Associated Proteins Creatine Kinase Lamin Type A Laminin Membrane Proteins Cytoskeletal Proteins Dystrophin-Associated Protein Complex Caveolin 3 Poly(A)-Binding Protein II Ubiquitin-Protein Ligases Calpain Plectin Eye Proteins RNA, Messenger Connectin Membrane Glycoproteins DNA DNA Primers Myostatin Lamins Proteins Mannosyltransferases N-Acetylglucosaminyltransferases Nerve Tissue Proteins Nuclear Proteins Carrier Proteins Creatine Kinase, MM Form Extracellular Matrix Proteins RNA Splice Sites Morpholinos Poly(A)-Binding Protein I Oxepins Codon, Terminator Integrin alpha Chains Evans Blue Pregnenediones Survival of Motor Neuron 1 Protein DNA, Complementary

Analytical, Diagnostic and Therapeutic Techniques and Equipment23

Pedigree DNA Mutational Analysis Chromosome Mapping Heterozygote Detection Disease Models, Animal Polymerase Chain Reaction Electroretinography Genetic Testing Genetic Therapy Immunohistochemistry Prenatal Diagnosis Blotting, Western Biopsy Muscle Strength Sequence Analysis, DNA Reverse Transcriptase Polymerase Chain Reaction Crosses, Genetic Fluorescent Antibody Technique Models, Genetic Case-Control Studies Blotting, Southern Amino Acid Substitution Magnetic Resonance Imaging

Psychiatry and Psychology3

Intellectual Disability Family Siblings

Phenomena and Processes62

Genes, Recessive Consanguinity Mutation Genetic Linkage Homozygote Mutation, Missense Lod Score Exons Phenotype Heterozygote Haplotypes Base Sequence Genetic Markers Amino Acid Sequence Genes, Dominant Codon, Nonsense X Chromosome Genotype Chromosomes, Human, Pair 4 Microsatellite Repeats Frameshift Mutation Alleles Founder Effect Point Mutation Polymorphism, Single-Stranded Conformational Genetic Heterogeneity Sequence Deletion Gene Deletion Chromosomes, Human, Pair 2 Exome Regeneration Muscle Development Muscle Strength Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 19 Gene Expression Regulation Glycosylation Polymorphism, Genetic Genetic Predisposition to Disease Introns Chromosomes, Human, Pair 5 Gene Expression Trinucleotide Repeat Expansion Polymorphism, Restriction Fragment Length Chromosome Deletion Alternative Splicing Sequence Homology, Amino Acid Chromosomes, Human, Pair 6 Protein Structure, Tertiary RNA Splice Sites Chromosomes, Human, Pair 10 RNA Splicing Genetic Vectors Polymorphism, Single Nucleotide Codon, Terminator Gene Frequency Signal Transduction Time Factors Amino Acid Substitution Mosaicism Protein Binding Transgenes

Disciplines and Occupations2

Immunohistochemistry Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena2

Family Siblings

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups4

Infant, Newborn Arabs Siblings Jews

Health Care5

Family Health Genetic Testing Age of Onset Genetic Counseling Case-Control Studies

Geographicals2

Pakistan Tunisia

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 Named Groups Health Care Geographicals

Genes, Recessive Muscular Dystrophies Muscular Dystrophy, Duchenne Pedigree Muscular Dystrophy, Animal Consanguinity Dystrophin Mutation Genetic Linkage Muscular Dystrophies, Limb-Girdle Myotonic Dystrophy Granulomatous Disease, Chronic DNA Mutational Analysis Homozygote Muscular Dystrophy, Facioscapulohumeral Spastic Paraplegia, Hereditary Chromosome Mapping Mutation, Missense Lod Score Mice, Inbred mdx Syndrome Muscular Dystrophy, Emery-Dreifuss Exons Sarcoglycans Phenotype Heterozygote Immunologic Deficiency Syndromes Corneal Dystrophies, Hereditary Haplotypes Molecular Sequence Data Dystroglycans Base Sequence Muscular Dystrophy, Oculopharyngeal Genetic Markers Utrophin Muscle, Skeletal Amino Acid Sequence Parkinson Disease Genes, Dominant Arthrogryposis Dysostoses Abnormalities, Multiple Codon, Nonsense X Chromosome Fuchs' Endothelial Dystrophy Retinal Dystrophies Polycystic Kidney, Autosomal Recessive Heterozygote Detection Thymopoietins Collagen Type VI Hearing Loss, Sensorineural Ectodermal Dysplasia Genotype Deafness Collagen Type XI Retinitis Pigmentosa Charcot-Marie-Tooth Disease Family Health Disease Models, Animal Sarcolemma Chromosomes, Human, Pair 4 Muscle Proteins Dystrophin-Associated Proteins Osteogenesis Imperfecta Muscular Diseases Creatine Kinase Microsatellite Repeats Muscles Myoblasts Muscle Fibers, Skeletal Lamin Type A Laminin Frameshift Mutation Membrane Proteins Intellectual Disability Cytoskeletal Proteins Dystrophin-Associated Protein Complex Caveolin 3 Neuromuscular Diseases Neuroaxonal Dystrophies Poly(A)-Binding Protein II Ubiquitin-Protein Ligases Alleles Microcephaly Walker-Warburg Syndrome Hypotrichosis Polymerase Chain Reaction Electroretinography Cardiomyopathies Infant, Newborn Mice, Inbred C57BL Genetic Testing Ichthyosis Founder Effect Calpain Retinal Degeneration Point Mutation Vitelliform Macular Dystrophy Sarcoglycanopathies Age of Onset

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