Muscle atrophy group muscular atrophy spinal. Medical search. Frequent questions

Home page Questions and answers Statistics Donations Contact

Anatomy63

Spinal Cord Muscle, Skeletal Muscles Muscle Fibers, Skeletal Motor Neurons Anterior Horn Cells Muscle, Smooth Muscle, Smooth, Vascular Muscle Fibers, Slow-Twitch Muscle Fibers, Fast-Twitch Mitochondria, Muscle Satellite Cells, Skeletal Muscle Spinal Nerve Roots Chromosomes, Human, Pair 5 Hindlimb Spinal Nerves Neuromuscular Junction Coiled Bodies Quadriceps Muscle Spinal Canal Muscle Cells Axons Myoblasts Myofibrils Myocytes, Smooth Muscle Cells, Cultured Neck Muscles Oculomotor Muscles Muscle, Striated Muscle Spindles Diaphragm Brain Respiratory Muscles Myoblasts, Skeletal Sciatic Nerve Velopharyngeal Sphincter Leg Papillary Muscles Cell Line Abdominal Muscles Masseter Muscle Facial Muscles Masticatory Muscles Sural Nerve Intercostal Muscles Inclusion Bodies Ganglia, Spinal Pectoralis Muscles Intranuclear Inclusion Bodies Ulnar Nerve Neurons Spine Peripheral Nerves Fibroblasts Thigh Lumbosacral Region Thoracic Vertebrae Cell Nucleus Arm Cervical Vertebrae Spliceosomes Acanthocytes Psoas Muscles

Organisms8

Mice, Transgenic Rats, Sprague-Dawley Mice, Inbred C57BL Mice, Knockout Rats, Wistar Animals, Newborn Rabbits Cats

Diseases60

Muscular Atrophy, Spinal Muscular Atrophy Atrophy Spinal Muscular Atrophies of Childhood Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Spinal Cord Injuries Optic Atrophy Muscle Weakness Multiple System Atrophy Disease Models, Animal Motor Neuron Disease Spinal Cord Diseases Olivopontocerebellar Atrophies Neuromuscular Diseases Muscular Diseases Cachexia Gyrate Atrophy Geographic Atrophy Nerve Degeneration Spinal Cord Neoplasms Sarcopenia Spinal Diseases Spinal Cord Compression Amyotrophic Lateral Sclerosis Spinal Neoplasms Bulbar Palsy, Progressive Hypertrophy Contracture Charcot-Marie-Tooth Disease Spinal Stenosis Optic Atrophy, Autosomal Dominant Arthrogryposis Wasting Syndrome Vocal Cord Paralysis Paralysis Muscular Dystrophies Spinal Injuries Neuromuscular Junction Diseases Myoclonic Epilepsies, Progressive Body Weight Spinal Cord Ischemia Disease Progression Fasciculation Paraplegia Gastritis, Atrophic Respiratory Paralysis Ophthalmoplegia Lameness, Animal Hammer Toe Syndrome Myositis Hereditary Sensory and Motor Neuropathy Neurodegenerative Diseases Optic Atrophies, Hereditary Scoliosis Postpoliomyelitis Syndrome Cerebellar Ataxia Tuberculosis, Spinal Syndrome Spinal Curvatures

Chemicals and Drugs37

Survival of Motor Neuron 1 Protein SMN Complex Proteins Survival of Motor Neuron 2 Protein Muscle Proteins SKP Cullin F-Box Protein Ligases Neuronal Apoptosis-Inhibitory Protein Cyclic AMP Response Element-Binding Protein RNA-Binding Proteins Myostatin Nerve Tissue Proteins Ribonucleoproteins, Small Nuclear DEAD Box Protein 20 Ubiquitin-Protein Ligases Myosin Heavy Chains Receptors, Androgen RNA, Messenger snRNP Core Proteins Proteasome Endopeptidase Complex Myogenin Glycine-tRNA Ligase Insulin-Like Growth Factor I Forkhead Transcription Factors MyoD Protein Ubiquitin Proto-Oncogene Proteins c-akt Skeletal Muscle Myosins Superoxide Dismutase Glucocorticoids Actins Protein Isoforms Transcription Factors Ribosomal Protein S6 Kinases, 70-kDa Calpain RNA Valproic Acid Myogenic Regulatory Factor 5 Dexamethasone

Analytical, Diagnostic and Therapeutic Techniques and Equipment35

Hindlimb Suspension Muscle Denervation Disease Models, Animal Immobilization Electromyography Magnetic Resonance Imaging Organ Size Injections, Spinal Anesthesia, Spinal Bed Rest Pedigree Muscle Strength Spinal Fusion Immunohistochemistry Heterozygote Detection Electric Stimulation Blotting, Western Reverse Transcriptase Polymerase Chain Reaction Models, Biological Electric Stimulation Therapy Analysis of Variance Weightlessness Countermeasures Body Weight Muscle Strength Dynamometer Polymerase Chain Reaction Weightlessness Simulation Myelography Biopsy Prenatal Diagnosis Resistance Training Tenotomy Genetic Therapy Laminectomy Genetic Testing Rotarod Performance Test

Psychiatry and Psychology1

Phenomena and Processes50

Muscle Contraction Muscle Development Muscle Fatigue Exons Chromosomes, Human, Pair 5 Organ Size Phenotype Time Factors Gene Expression Regulation Neural Conduction Isometric Contraction Signal Transduction Mutation Muscle Strength Aging Muscle Relaxation Proteolysis Motor Activity Gene Deletion Gene Expression Homozygote Trinucleotide Repeat Expansion Base Sequence RNA Splicing Estivation Genes, Recessive Weightlessness Weight-Bearing Genetic Linkage Trinucleotide Repeats Genes, Dominant Biomechanical Phenomena Recovery of Function Regeneration Body Weight Gene Dosage Cell Differentiation Amino Acid Sequence Oxidative Stress Alternative Splicing Mutation, Missense Apoptosis Resistance Training Phosphorylation Locomotion Transcription, Genetic Action Potentials Protein Binding Physical Conditioning, Animal Dose-Response Relationship, Drug

Disciplines and Occupations3

Immunohistochemistry Chemistry, Analytic Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

Resistance Training

Technology, Industry, Agriculture1

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care6

Hindlimb Suspension Analysis of Variance Weightlessness Simulation 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 Technology, Industry, Agriculture Information Science Health Care

Muscular Atrophy, Spinal Muscular Atrophy Atrophy Spinal Muscular Atrophies of Childhood Survival of Motor Neuron 1 Protein SMN Complex Proteins Survival of Motor Neuron 2 Protein Spinal Cord Muscular Disorders, Atrophic Muscle, Skeletal Muscle Proteins Hindlimb Suspension Muscles SKP Cullin F-Box Protein Ligases Muscle Fibers, Skeletal Bulbo-Spinal Atrophy, X-Linked Spinal Cord Injuries Motor Neurons Neuronal Apoptosis-Inhibitory Protein Optic Atrophy Muscle Denervation Cyclic AMP Response Element-Binding Protein Anterior Horn Cells RNA-Binding Proteins Myostatin Muscle, Smooth Muscle Weakness Muscle Contraction Multiple System Atrophy Muscle Development Nerve Tissue Proteins Disease Models, Animal Motor Neuron Disease Muscle, Smooth, Vascular Muscle Fibers, Slow-Twitch Muscle Fibers, Fast-Twitch Spinal Cord Diseases Immobilization Electromyography Ribonucleoproteins, Small Nuclear Mice, Transgenic Muscle Fatigue DEAD Box Protein 20 Mitochondria, Muscle Olivopontocerebellar Atrophies Magnetic Resonance Imaging Neuromuscular Diseases Muscular Diseases Satellite Cells, Skeletal Muscle Spinal Nerve Roots Exons Chromosomes, Human, Pair 5 Organ Size Ubiquitin-Protein Ligases Cachexia Gyrate Atrophy Injections, Spinal Hindlimb Spinal Nerves Neuromuscular Junction Coiled Bodies Quadriceps Muscle Rats, Sprague-Dawley Phenotype Myosin Heavy Chains Receptors, Androgen RNA, Messenger Anesthesia, Spinal snRNP Core Proteins Geographic Atrophy Time Factors Gene Expression Regulation Mice, Inbred C57BL Bed Rest Neural Conduction Pedigree Nerve Degeneration Isometric Contraction Spinal Cord Neoplasms Spinal Canal Signal Transduction Mice, Knockout Muscle Cells Sarcopenia Axons Myoblasts Spinal Diseases Spinal Cord Compression Myofibrils Myocytes, Smooth Muscle Amyotrophic Lateral Sclerosis Cells, Cultured Mutation Space Flight Neck Muscles Proteasome Endopeptidase Complex Oculomotor Muscles Spinal Neoplasms Rats, Wistar Bulbar Palsy, Progressive

No FAQ available that match "muscle atrophy group muscular atrophy spinal"