Smn1 affects muscular atrophy spinal. Medical search. Frequent questions

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Anatomy38

Spinal Cord Motor Neurons Anterior Horn Cells Coiled Bodies Chromosomes, Human, Pair 5 Spinal Nerve Roots Spinal Nerves Spinal Canal Muscle, Skeletal Axons Neuromuscular Junction Spliceosomes Ganglia, Spinal Sural Nerve Intranuclear Inclusion Bodies HeLa Cells Fibroblasts Brain Inclusion Bodies Spine Thoracic Vertebrae Ulnar Nerve Muscles Neurons Acanthocytes Cervical Vertebrae Cells, Cultured Sciatic Nerve Posterior Horn Cells Muscle Fibers, Skeletal Peripheral Nerves Growth Cones Lumbosacral Region Cell Line Lumbar Vertebrae Central Nervous System Cell Nucleus Neurites

Organisms6

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

Diseases48

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 Spinal Cord Neoplasms Spinal Diseases Spinal Cord Compression Spinal Neoplasms Bulbar Palsy, Progressive Spinal Stenosis Nerve Degeneration Charcot-Marie-Tooth Disease Muscle Weakness Contracture Olivopontocerebellar Atrophies Neuromuscular Diseases Arthrogryposis Neuromuscular Junction Diseases Vocal Cord Paralysis Spinal Injuries Gyrate Atrophy Amyotrophic Lateral Sclerosis Spinal Cord Ischemia Geographic Atrophy Paraplegia Fasciculation Myoclonic Epilepsies, Progressive Respiratory Paralysis Tuberculosis, Spinal Scoliosis Spinal Curvatures Postpoliomyelitis Syndrome Muscular Dystrophies Hematoma, Epidural, Spinal Hereditary Sensory and Motor Neuropathy Optic Atrophy, Autosomal Dominant Disease Progression Ophthalmoplegia Muscular Diseases Neurodegenerative Diseases

Chemicals and Drugs22

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment22

Disease Models, Animal Injections, Spinal Anesthesia, Spinal Pedigree Heterozygote Detection Electromyography Spinal Fusion Magnetic Resonance Imaging Myelography Prenatal Diagnosis Genetic Testing Genetic Therapy Rotarod Performance Test Laminectomy Immunohistochemistry Muscle Denervation Blotting, Western Polymerase Chain Reaction DNA Mutational Analysis Muscle Strength Chromosome Mapping Muscle Strength Dynamometer

Psychiatry and Psychology1

Phenomena and Processes26

Exons Chromosomes, Human, Pair 5 Phenotype RNA Splicing Gene Deletion Homozygote Mutation Gene Dosage Neural Conduction Trinucleotide Repeat Expansion Alternative Splicing Genes, Recessive Motor Activity Genetic Linkage Trinucleotide Repeats Genes, Dominant Base Sequence Mutation, Missense Time Factors Gene Expression Regulation Heterozygote Muscle Strength Founder Effect Introns Gene Expression Amino Acid Sequence

Disciplines and Occupations3

Chemistry, Analytic Genetic Counseling Immunohistochemistry

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care3

Genetic Testing Genetic Counseling Age of Onset

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 Cyclic AMP Response Element-Binding Protein Bulbo-Spinal Atrophy, X-Linked Neuronal Apoptosis-Inhibitory Protein Spinal Cord Injuries Motor Neurons RNA-Binding Proteins Anterior Horn Cells Nerve Tissue Proteins Ribonucleoproteins, Small Nuclear DEAD Box Protein 20 Spinal Cord Diseases Optic Atrophy Coiled Bodies Motor Neuron Disease Exons snRNP Core Proteins Chromosomes, Human, Pair 5 Disease Models, Animal Spinal Nerve Roots Injections, Spinal Spinal Nerves Multiple System Atrophy Anesthesia, Spinal Receptors, Androgen Spinal Cord Neoplasms Spinal Canal Muscle, Skeletal Spinal Diseases Spinal Cord Compression Mice, Transgenic Spinal Neoplasms Pedigree Heterozygote Detection Phenotype Bulbar Palsy, Progressive Spinal Stenosis Electromyography Spinal Fusion RNA Splicing Gene Deletion Nerve Degeneration Axons Homozygote Charcot-Marie-Tooth Disease Muscle Weakness Magnetic Resonance Imaging Contracture Mutation Olivopontocerebellar Atrophies Neuromuscular Diseases Gene Dosage Glycine-tRNA Ligase Arthrogryposis Neural Conduction Neuromuscular Junction Neuromuscular Junction Diseases Vocal Cord Paralysis Spinal Injuries Gyrate Atrophy Amyotrophic Lateral Sclerosis Spliceosomes Trinucleotide Repeat Expansion Alternative Splicing Genes, Recessive Spinal Cord Ischemia Ganglia, Spinal Sural Nerve Motor Activity Geographic Atrophy Genetic Linkage Trinucleotide Repeats Genes, Dominant Molecular Sequence Data Intranuclear Inclusion Bodies Myelography HeLa Cells Valproic Acid Fibroblasts Brain Prenatal Diagnosis Inclusion Bodies Paraplegia Base Sequence Fasciculation Myoclonic Epilepsies, Progressive Genetic Testing Chemistry, Analytic Genetic Counseling Spine Thoracic Vertebrae Aclarubicin

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