Neuronal infantile muscular atrophy spinal. Medical search. Frequent questions

Home page Questions and answers Statistics Donations Contact

Anatomy53

Spinal Cord Motor Neurons Anterior Horn Cells Neurons Spinal Nerve Roots Chromosomes, Human, Pair 5 Spinal Nerves Coiled Bodies Brain Axons Spinal Canal Muscle, Skeletal Cells, Cultured Ganglia, Spinal Neuromuscular Junction Hippocampus Neurites Cerebral Cortex Inclusion Bodies Intranuclear Inclusion Bodies Sural Nerve Synapses Neuroglia Growth Cones Muscles Cell Line Spine Thoracic Vertebrae Sciatic Nerve Ulnar Nerve Peripheral Nerves Spliceosomes Acanthocytes Astrocytes Cervical Vertebrae Fibroblasts Lumbosacral Region Cerebellum Posterior Horn Cells Muscle Fibers, Skeletal HeLa Cells Lumbar Vertebrae Cell Nucleus Brain Stem Neurons, Afferent Nerve Net Interneurons PC12 Cells Neural Pathways Dendrites Trigeminal Nucleus, Spinal Central Nervous System Arm

Organisms11

Mice, Transgenic Rats, Sprague-Dawley Mice, Knockout Animals, Newborn Mice, Inbred C57BL Rats, Wistar Mice, Mutant Strains Animals, Genetically Modified Mice, Neurologic Mutants Cats Zebrafish

Diseases55

Muscular Atrophy, Spinal Spinal Muscular Atrophies of Childhood Atrophy Muscular Atrophy Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Spinal Cord Injuries Spinal Cord Diseases Optic Atrophy Motor Neuron Disease Disease Models, Animal Multiple System Atrophy Nerve Degeneration Spinal Cord Neoplasms Spinal Cord Compression Spinal Diseases Spinal Neoplasms Bulbar Palsy, Progressive Spinal Stenosis Charcot-Marie-Tooth Disease Muscle Weakness Olivopontocerebellar Atrophies Contracture Neuromuscular Diseases Arthrogryposis Vocal Cord Paralysis Amyotrophic Lateral Sclerosis Spinal Injuries Gyrate Atrophy Neuromuscular Junction Diseases Spinal Cord Ischemia Neurodegenerative Diseases Geographic Atrophy Myoclonic Epilepsies, Progressive Fasciculation Paraplegia Respiratory Paralysis Tuberculosis, Spinal Scoliosis Spinal Curvatures Muscular Dystrophies Neuronal Ceroid-Lipofuscinoses Disease Progression Postpoliomyelitis Syndrome Hematoma, Epidural, Spinal Hereditary Sensory and Motor Neuropathy Nervous System Diseases Optic Atrophy, Autosomal Dominant Alzheimer Disease Ophthalmoplegia Muscular Diseases Pain Tremor Spinal Fractures Syndrome

Chemicals and Drugs27

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 Nerve Tissue Proteins RNA-Binding Proteins Ribonucleoproteins, Small Nuclear DEAD Box Protein 20 Receptors, Androgen snRNP Core Proteins Glycine-tRNA Ligase Neurofilament Proteins Neuroprotective Agents Nitric Oxide Synthase Type I Valproic Acid Furylfuramide Peptides RNA, Messenger Aclarubicin Green Fluorescent Proteins DNA Primers Oligonucleotides, Antisense Heterogeneous-Nuclear Ribonucleoprotein Group A-B Nerve Growth Factors Glutamic Acid Enzyme Inhibitors

Analytical, Diagnostic and Therapeutic Techniques and Equipment29

Disease Models, Animal Injections, Spinal Anesthesia, Spinal Pedigree Magnetic Resonance Imaging Electromyography Spinal Fusion Heterozygote Detection Immunohistochemistry Myelography Blotting, Western Rotarod Performance Test Prenatal Diagnosis Laminectomy Genetic Testing Electric Stimulation Muscle Denervation Genetic Therapy Analysis of Variance Polymerase Chain Reaction Muscle Strength Chromosome Mapping Models, Biological DNA Mutational Analysis Muscle Strength Dynamometer Hindlimb Suspension Models, Neurological Severity of Illness Index Transfection

Psychiatry and Psychology4

Motor Activity Alzheimer Disease Behavior, Animal Pain

Phenomena and Processes42

Chromosomes, Human, Pair 5 Exons Phenotype Mutation Neural Conduction Neuronal Plasticity Gene Deletion Homozygote Time Factors Trinucleotide Repeat Expansion RNA Splicing Motor Activity Action Potentials Genes, Recessive Gene Expression Regulation Genetic Linkage Gene Dosage Trinucleotide Repeats Genes, Dominant Base Sequence Alternative Splicing Cell Differentiation Mutation, Missense Signal Transduction Amino Acid Sequence Cell Death Cell Survival Dose-Response Relationship, Drug Neurogenesis Synaptic Transmission Apoptosis Muscle Strength Protein Binding Heterozygote Locomotion Founder Effect Pain Spinal Cord Regeneration Recovery of Function Alleles Genotype Transfection

Disciplines and Occupations4

Immunohistochemistry Chemistry, Analytic Genetic Counseling Electrophysiology

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care6

Genetic Counseling Genetic Testing Analysis of Variance Age of Onset Hindlimb Suspension Severity of Illness Index

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 Survival of Motor Neuron 1 Protein Atrophy SMN Complex Proteins Muscular Atrophy Survival of Motor Neuron 2 Protein Spinal Cord Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Spinal Cord Injuries Neuronal Apoptosis-Inhibitory Protein Cyclic AMP Response Element-Binding Protein Motor Neurons Anterior Horn Cells Nerve Tissue Proteins RNA-Binding Proteins Spinal Cord Diseases Optic Atrophy Motor Neuron Disease Ribonucleoproteins, Small Nuclear Disease Models, Animal DEAD Box Protein 20 Neurons Spinal Nerve Roots Injections, Spinal Chromosomes, Human, Pair 5 Exons Spinal Nerves Multiple System Atrophy Coiled Bodies Anesthesia, Spinal Nerve Degeneration Mice, Transgenic Receptors, Androgen snRNP Core Proteins Brain Axons Spinal Cord Neoplasms Spinal Canal Muscle, Skeletal Spinal Cord Compression Spinal Diseases Spinal Neoplasms Pedigree Phenotype Magnetic Resonance Imaging Rats, Sprague-Dawley Electromyography Bulbar Palsy, Progressive Spinal Stenosis Mutation Spinal Fusion Cells, Cultured Charcot-Marie-Tooth Disease Muscle Weakness Heterozygote Detection Neural Conduction Neuronal Plasticity Ganglia, Spinal Olivopontocerebellar Atrophies Contracture Gene Deletion Neuromuscular Diseases Glycine-tRNA Ligase Arthrogryposis Immunohistochemistry Homozygote Neuromuscular Junction Vocal Cord Paralysis Hippocampus Time Factors Amyotrophic Lateral Sclerosis Trinucleotide Repeat Expansion Spinal Injuries Mice, Knockout Neurites Gyrate Atrophy Animals, Newborn RNA Splicing Molecular Sequence Data Motor Activity Neuromuscular Junction Diseases Mice, Inbred C57BL Cerebral Cortex Spinal Cord Ischemia Inclusion Bodies Action Potentials Genes, Recessive Intranuclear Inclusion Bodies Gene Expression Regulation Genetic Linkage Gene Dosage Sural Nerve Neurodegenerative Diseases Neurofilament Proteins Trinucleotide Repeats Genes, Dominant Geographic Atrophy Neuroprotective Agents

No FAQ available that match "neuronal infantile muscular atrophy spinal"