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Anatomy51

Spinal Cord Motor Neurons Anterior Horn Cells Spinal Nerves Spinal Nerve Roots Spinal Canal Chromosomes, Human, Pair 5 Coiled Bodies Ganglia, Spinal Muscle, Skeletal Axons Spine Thoracic Vertebrae Posterior Horn Cells Cervical Vertebrae Lumbosacral Region Lumbar Vertebrae Neuromuscular Junction Neurons Sural Nerve Trigeminal Nucleus, Spinal Brain Sciatic Nerve Muscles Intranuclear Inclusion Bodies Peripheral Nerves Epidural Space Inclusion Bodies Ulnar Nerve Central Nervous System Nociceptors Spliceosomes Hindlimb Afferent Pathways Acanthocytes Cells, Cultured Neurons, Afferent Muscle Fibers, Skeletal Fibroblasts Growth Cones Synapses HeLa Cells Interneurons Brain Stem Arm Dura Mater Cauda Equina Neurites Sacrum Pyramidal Tracts Cell Line

Organisms8

Mice, Transgenic Rats, Sprague-Dawley Animals, Newborn Mice, Knockout Mice, Inbred C57BL Cats Mice, Neurologic Mutants Lampreys

Diseases67

Muscular Atrophy, Spinal Spinal Muscular Atrophies of Childhood Atrophy Muscular Atrophy Spinal Cord Injuries Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Spinal Cord Diseases Spinal Cord Neoplasms Spinal Diseases Spinal Cord Compression Spinal Neoplasms Motor Neuron Disease Optic Atrophy Spinal Stenosis Disease Models, Animal Spinal Injuries Spinal Cord Ischemia Multiple System Atrophy Paraplegia Tuberculosis, Spinal Spinal Curvatures Bulbar Palsy, Progressive Nerve Degeneration Hematoma, Epidural, Spinal Muscle Weakness Neuromuscular Diseases Charcot-Marie-Tooth Disease Contracture Olivopontocerebellar Atrophies Arthrogryposis Amyotrophic Lateral Sclerosis Spinal Fractures Vocal Cord Paralysis Scoliosis Gyrate Atrophy Quadriplegia Neuromuscular Junction Diseases Pain Hyperalgesia Geographic Atrophy Respiratory Paralysis Neuralgia Fasciculation Myoclonic Epilepsies, Progressive Paralysis Myelitis Disease Progression Postpoliomyelitis Syndrome Muscular Dystrophies Hereditary Sensory and Motor Neuropathy Spinal Dysraphism Hematoma, Subdural, Spinal Optic Atrophy, Autosomal Dominant Spinal Osteophytosis Ophthalmoplegia Muscular Diseases Nervous System Diseases Neurodegenerative Diseases Syndrome Kyphosis Urinary Bladder, Neurogenic Spinal Cord Vascular Diseases Tremor Paraparesis Decerebrate State Muscle Spasticity

Chemicals and Drugs22

Survival of Motor Neuron 1 Protein SMN Complex Proteins Survival of Motor Neuron 2 Protein Neuronal Apoptosis-Inhibitory Protein Cyclic AMP Response Element-Binding Protein RNA-Binding Proteins Nerve Tissue Proteins Ribonucleoproteins, Small Nuclear DEAD Box Protein 20 Receptors, Androgen snRNP Core Proteins Glycine-tRNA Ligase RNA, Messenger Neurofilament Proteins Valproic Acid Furylfuramide Aclarubicin Analgesics Peptides Heterogeneous-Nuclear Ribonucleoprotein Group A-B Neuroprotective Agents Oligonucleotides, Antisense

Analytical, Diagnostic and Therapeutic Techniques and Equipment37

Injections, Spinal Anesthesia, Spinal Spinal Fusion Disease Models, Animal Electromyography Magnetic Resonance Imaging Pedigree Laminectomy Myelography Heterozygote Detection Manipulation, Spinal Immunohistochemistry Cordotomy Pain Measurement Spinal Puncture Prenatal Diagnosis Electric Stimulation Reflex Spinal Cord Stimulation Genetic Testing Muscle Denervation Decompression, Surgical Genetic Therapy Rotarod Performance Test Physical Stimulation Muscle Strength Treatment Outcome Electric Stimulation Therapy Blotting, Western Polymerase Chain Reaction Severity of Illness Index Chromosome Mapping Muscle Strength Dynamometer DNA Mutational Analysis Analysis of Variance Hindlimb Suspension Retrospective Studies

Psychiatry and Psychology3

Motor Activity Pain Reflex

Phenomena and Processes32

Chromosomes, Human, Pair 5 Exons Neural Conduction Phenotype Gene Deletion Mutation Motor Activity Spinal Cord Regeneration Homozygote RNA Splicing Trinucleotide Repeat Expansion Pain Time Factors Genes, Recessive Locomotion Genetic Linkage Gene Dosage Trinucleotide Repeats Recovery of Function Genes, Dominant Nerve Regeneration Alternative Splicing Reflex Base Sequence Mutation, Missense Gene Expression Regulation Action Potentials Muscle Strength Founder Effect Heterozygote Gene Expression Dose-Response Relationship, Drug

Disciplines and Occupations3

Immunohistochemistry Chemistry, Analytic Genetic Counseling

Information Science2

Molecular Sequence Data Base Sequence

Health Care8

Genetic Counseling Genetic Testing Age of Onset Treatment Outcome Severity of Illness Index Analysis of Variance Hindlimb Suspension Retrospective Studies

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 Atrophy, Spinal Spinal Muscular Atrophies of Childhood Spinal Cord Survival of Motor Neuron 1 Protein Atrophy SMN Complex Proteins Muscular Atrophy Survival of Motor Neuron 2 Protein Spinal Cord Injuries Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Neuronal Apoptosis-Inhibitory Protein Motor Neurons Anterior Horn Cells Cyclic AMP Response Element-Binding Protein Spinal Cord Diseases Injections, Spinal Spinal Nerves RNA-Binding Proteins Spinal Nerve Roots Anesthesia, Spinal Nerve Tissue Proteins Spinal Cord Neoplasms Spinal Canal Spinal Diseases Spinal Cord Compression Spinal Neoplasms Motor Neuron Disease Optic Atrophy Spinal Stenosis Spinal Fusion Ribonucleoproteins, Small Nuclear DEAD Box Protein 20 Disease Models, Animal Chromosomes, Human, Pair 5 Spinal Injuries Exons Coiled Bodies Spinal Cord Ischemia Ganglia, Spinal Multiple System Atrophy Muscle, Skeletal Receptors, Androgen snRNP Core Proteins Electromyography Axons Paraplegia Magnetic Resonance Imaging Spine Mice, Transgenic Thoracic Vertebrae Tuberculosis, Spinal Pedigree Laminectomy Spinal Curvatures Bulbar Palsy, Progressive Nerve Degeneration Hematoma, Epidural, Spinal Posterior Horn Cells Neural Conduction Cervical Vertebrae Muscle Weakness Myelography Phenotype Neuromuscular Diseases Lumbosacral Region Charcot-Marie-Tooth Disease Heterozygote Detection Lumbar Vertebrae Contracture Rats, Sprague-Dawley Olivopontocerebellar Atrophies Arthrogryposis Glycine-tRNA Ligase Amyotrophic Lateral Sclerosis Gene Deletion Spinal Fractures Vocal Cord Paralysis Mutation Motor Activity Spinal Cord Regeneration Scoliosis Neuromuscular Junction Homozygote Neurons Gyrate Atrophy RNA Splicing Quadriplegia Trinucleotide Repeat Expansion Neuromuscular Junction Diseases Sural Nerve Trigeminal Nucleus, Spinal Pain Time Factors Hyperalgesia Brain Manipulation, Spinal Genes, Recessive Locomotion Sciatic Nerve

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