Progressive muscle weakness survival of motor neuron 1 protein. Medical search. Frequent questions

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Anatomy72

Motor Neurons Muscle, Skeletal Neurons Muscles Muscle Fibers, Skeletal Neurons, Afferent Motor Cortex Spinal Cord Respiratory Muscles Muscle, Smooth Muscle, Smooth, Vascular Axons Neuromuscular Junction Cells, Cultured Diaphragm Muscle Fibers, Slow-Twitch Muscle Fibers, Fast-Twitch Quadriceps Muscle Mitochondria, Muscle Synapses Brain Oculomotor Muscles Ganglia, Invertebrate Neck Muscles Muscle Spindles Interneurons Myocytes, Smooth Muscle Muscle, Striated Cholinergic Neurons Anterior Horn Cells Dopaminergic Neurons Sensory Receptor Cells Facial Muscles Dendrites Ganglia, Spinal Extremities Cerebral Cortex Facial Nerve Peripheral Nerves GABAergic Neurons Hindlimb Papillary Muscles Brain Stem Hippocampus Abdominal Muscles Chick Embryo Central Nervous System Myofibrils Muscle Cells Masseter Muscle Masticatory Muscles Neurons, Efferent Medulla Oblongata Ganglia Afferent Pathways Nerve Net Cell Line Intercostal Muscles Cerebellum Neuroglia Sciatic Nerve Olfactory Receptor Neurons Astrocytes Mesencephalon Pharyngeal Muscles Myoblasts Sarcomeres Hand Satellite Cells, Skeletal Muscle Neurites Rhombencephalon Nervous System

Organisms15

Mice, Inbred mdx Mice, Transgenic Mice, Inbred C57BL Mice, Knockout Rats, Sprague-Dawley Animals, Newborn Rats, Wistar Aplysia Cats Animals, Genetically Modified Grasshoppers Rabbits Zebrafish Caenorhabditis elegans Leeches

Diseases50

Muscle Weakness Myositis, Inclusion Body Muscular Dystrophy, Duchenne Motor Neuron Disease Muscular Dystrophies Muscular Diseases Muscular Atrophy, Spinal Muscular Atrophy Muscular Dystrophy, Animal Neuromuscular Diseases Disease Models, Animal Myopathies, Nemaline Amyotrophic Lateral Sclerosis Myositis Polymyositis Bulbar Palsy, Progressive Nerve Degeneration Dermatomyositis Hypokalemic Periodic Paralysis Myopathies, Structural, Congenital Myasthenia Gravis Paralysis Muscle Hypotonia Myasthenic Syndromes, Congenital Disease Progression Respiratory Paralysis Charcot-Marie-Tooth Disease Spinal Muscular Atrophies of Childhood Muscular Dystrophies, Limb-Girdle Ophthalmoplegia Rhabdomyolysis Distal Myopathies Hereditary Sensory and Motor Neuropathy Myotonic Dystrophy Muscle Spasticity Lambert-Eaton Myasthenic Syndrome Hypokalemia Syndrome Postpoliomyelitis Syndrome Glycogen Storage Disease Type II Respiratory Insufficiency Neuromuscular Junction Diseases Peripheral Nervous System Diseases Myotonia Paralyses, Familial Periodic Spinal Cord Diseases Paresis Reflex, Abnormal Mitochondrial Myopathies Movement Disorders

Chemicals and Drugs28

Dystrophin Survival of Motor Neuron 1 Protein Muscle Proteins Survival of Motor Neuron 2 Protein SMN Complex Proteins Nerve Tissue Proteins Molecular Motor Proteins Superoxide Dismutase Calcium RNA, Messenger Receptors, Cholinergic Myosin Heavy Chains Neuropeptides Green Fluorescent Proteins gamma-Aminobutyric Acid Choline O-Acetyltransferase Neurofilament Proteins Nerve Growth Factors Creatine Kinase Glutamic Acid Actins Monocrotophos Transcription Factors Cyclic AMP Response Element-Binding Protein Dopamine Tetrodotoxin Serotonin Homeodomain Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment37

Relaxation Therapy Meditation Disease Models, Animal Survival Rate Electromyography Electric Stimulation Muscle Strength Immunohistochemistry Muscle Denervation Disease-Free Survival Treatment Outcome Survival Analysis Analysis of Variance Patch-Clamp Techniques Retrospective Studies Muscle Strength Dynamometer Models, Neurological Pedigree Cell Count Follow-Up Studies Models, Biological Blotting, Western Hand Strength Microscopy, Electron Biopsy Magnetic Resonance Imaging In Situ Hybridization Reflex Physical Stimulation Inspiratory Capacity Reverse Transcriptase Polymerase Chain Reaction Gait Neurologic Examination Reflex, Abnormal Severity of Illness Index Kaplan-Meier Estimate Prognosis

Psychiatry and Psychology9

Relaxation Therapy Meditation Motor Activity Motor Skills Disorders Behavior, Animal Reaction Time Psychomotor Performance Reflex Functional Laterality

Phenomena and Processes51

Muscle Contraction Cell Survival Evoked Potentials, Motor Motor Activity Time Factors Muscle Development Muscle Fatigue Action Potentials Muscle Strength Mutation Isometric Contraction Neural Conduction Movement Phenotype Synaptic Transmission Signal Transduction Membrane Potentials Graft Survival Cell Differentiation Muscle Relaxation Neural Inhibition Biomechanical Phenomena Gene Expression Regulation Locomotion Aging Gene Expression Regulation, Developmental Cell Count Dose-Response Relationship, Drug Apoptosis Hand Strength Axonal Transport Reaction Time Evoked Potentials Amino Acid Sequence Cell Death Psychomotor Performance Base Sequence Gene Expression Neuronal Plasticity Torque Recruitment, Neurophysiological Excitatory Postsynaptic Potentials Reflex Nerve Regeneration Inspiratory Capacity Periodicity Neurogenesis Gait Functional Laterality Reflex, Abnormal Inhalation

Disciplines and Occupations2

Immunohistochemistry Electrophysiology

Anthropology, Education, Sociology and Social Phenomena1

Information Science4

Survival Rate Molecular Sequence Data Amino Acid Sequence Base Sequence

Health Care11

Survival Rate Disease-Free Survival Treatment Outcome Survival Analysis Analysis of Variance Retrospective Studies Follow-Up Studies Age Factors Age of Onset Severity of Illness Index Kaplan-Meier Estimate

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

Muscle Weakness Myositis, Inclusion Body Muscular Dystrophy, Duchenne Motor Neurons Muscle, Skeletal Relaxation Therapy Motor Neuron Disease Neurons Muscles Muscular Dystrophies Muscular Diseases Muscular Atrophy, Spinal Dystrophin Muscle Fibers, Skeletal Muscular Atrophy Muscular Dystrophy, Animal Mice, Inbred mdx Meditation Survival of Motor Neuron 1 Protein Neuromuscular Diseases Neurons, Afferent Muscle Proteins Disease Models, Animal Muscle Contraction Myopathies, Nemaline Cell Survival Amyotrophic Lateral Sclerosis Motor Cortex Survival of Motor Neuron 2 Protein Mice, Transgenic Survival Rate Evoked Potentials, Motor Spinal Cord Respiratory Muscles Muscle, Smooth Electromyography Motor Activity Muscle, Smooth, Vascular Time Factors Axons Muscle Development Muscle Fatigue Neuromuscular Junction Electric Stimulation Cells, Cultured Action Potentials Myositis Polymyositis Diaphragm SMN Complex Proteins Muscle Strength Muscle Fibers, Slow-Twitch Immunohistochemistry Nerve Tissue Proteins Mutation Bulbar Palsy, Progressive Muscle Denervation Muscle Fibers, Fast-Twitch Quadriceps Muscle Mice, Inbred C57BL Disease-Free Survival Electrophysiology Isometric Contraction Mitochondria, Muscle Nerve Degeneration Dermatomyositis Survival Neural Conduction Synapses Movement Hypokalemic Periodic Paralysis Molecular Motor Proteins Treatment Outcome Phenotype Myopathies, Structural, Congenital Myasthenia Gravis Paralysis Superoxide Dismutase Survival Analysis Mice, Knockout Brain Oculomotor Muscles Ganglia, Invertebrate Synaptic Transmission Neck Muscles Muscle Hypotonia Calcium Signal Transduction Muscle Spindles Myasthenic Syndromes, Congenital Rats, Sprague-Dawley Interneurons Myocytes, Smooth Muscle Animals, Newborn Analysis of Variance RNA, Messenger Membrane Potentials Graft Survival Disease Progression Muscle, Striated

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