Spinal muscular atrophy survival of motor neuron 2 protein. Medical search. Frequent questions

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Anatomy38

Motor Neurons Spinal Cord Neurons Anterior Horn Cells Chromosomes, Human, Pair 5 Coiled Bodies Neurons, Afferent Axons Motor Cortex Neuromuscular Junction Muscle, Skeletal Cells, Cultured Spinal Nerve Roots Synapses Spinal Nerves Spliceosomes Muscles Ganglia, Spinal Brain Central Nervous System Growth Cones Neurites Fibroblasts Interneurons HeLa Cells Cell Line Ganglia, Invertebrate Spinal Canal Cholinergic Neurons Sensory Receptor Cells Peripheral Nerves Dendrites Cerebral Cortex Brain Stem Muscle Fibers, Skeletal Dopaminergic Neurons Sciatic Nerve Hippocampus

Organisms9

Mice, Transgenic Mice, Knockout Animals, Newborn Mice, Inbred C57BL Rats, Sprague-Dawley Zebrafish Animals, Genetically Modified Mice, Mutant Strains Aplysia

Diseases31

Muscular Atrophy, Spinal Spinal Muscular Atrophies of Childhood Muscular Atrophy Atrophy Motor Neuron Disease Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Spinal Cord Injuries Disease Models, Animal Amyotrophic Lateral Sclerosis Spinal Cord Diseases Nerve Degeneration Neuromuscular Diseases Neuromuscular Junction Diseases Arthrogryposis Optic Atrophy Fasciculation Bulbar Palsy, Progressive Charcot-Marie-Tooth Disease Contracture Muscle Weakness Vocal Cord Paralysis Hereditary Sensory and Motor Neuropathy Respiratory Paralysis Multiple System Atrophy Muscular Dystrophies Spinal Cord Neoplasms Spinal Cord Compression Disease Progression Spinal Diseases Spinal Neoplasms

Chemicals and Drugs24

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 snRNP Core Proteins Glycine-tRNA Ligase RNA, Messenger Valproic Acid Receptors, Androgen Molecular Motor Proteins Aclarubicin Superoxide Dismutase Heterogeneous-Nuclear Ribonucleoprotein Group A-B Oligonucleotides, Antisense Neurofilament Proteins DNA Primers Heterogeneous-Nuclear Ribonucleoproteins RNA, Small Nuclear Green Fluorescent Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment25

Disease Models, Animal Survival Rate Electromyography Pedigree Heterozygote Detection Immunohistochemistry Injections, Spinal Prenatal Diagnosis Electric Stimulation Survival Analysis Disease-Free Survival Genetic Testing Genetic Therapy Anesthesia, Spinal Blotting, Western Polymerase Chain Reaction Magnetic Resonance Imaging Models, Biological Reverse Transcriptase Polymerase Chain Reaction Muscle Strength Dynamometer Chromosome Mapping Treatment Outcome DNA Mutational Analysis Analysis of Variance Patch-Clamp Techniques

Psychiatry and Psychology1

Phenomena and Processes35

Chromosomes, Human, Pair 5 Exons Cell Survival Motor Activity Evoked Potentials, Motor Phenotype Mutation Gene Deletion Homozygote RNA Splicing Action Potentials Neural Conduction Time Factors Gene Dosage Genes, Dominant Genes, Recessive Alternative Splicing Genetic Linkage Base Sequence Gene Expression Regulation Mutation, Missense Synaptic Transmission Amino Acid Sequence Movement Cell Differentiation Heterozygote Gene Expression Graft Survival Apoptosis Signal Transduction Locomotion Protein Binding Neural Inhibition Genotype Alleles

Disciplines and Occupations4

Immunohistochemistry Chemistry, Analytic Genetic Counseling Electrophysiology

Anthropology, Education, Sociology and Social Phenomena1

Information Science4

Survival Rate Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care7

Survival Rate Survival Analysis Disease-Free Survival Genetic Counseling Genetic Testing Treatment Outcome Analysis of Variance

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

Muscular Atrophy, Spinal Spinal Muscular Atrophies of Childhood Survival of Motor Neuron 1 Protein SMN Complex Proteins Survival of Motor Neuron 2 Protein Motor Neurons Spinal Cord Muscular Atrophy Atrophy Neuronal Apoptosis-Inhibitory Protein Motor Neuron Disease Cyclic AMP Response Element-Binding Protein Neurons RNA-Binding Proteins Anterior Horn Cells Nerve Tissue Proteins Ribonucleoproteins, Small Nuclear DEAD Box Protein 20 Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Spinal Cord Injuries Chromosomes, Human, Pair 5 Exons Coiled Bodies Disease Models, Animal Amyotrophic Lateral Sclerosis Neurons, Afferent snRNP Core Proteins Cell Survival Axons Spinal Cord Diseases Motor Activity Mice, Transgenic Motor Cortex Evoked Potentials, Motor Survival Rate Nerve Degeneration Neuromuscular Diseases Neuromuscular Junction Electromyography Muscle, Skeletal Pedigree Phenotype Heterozygote Detection Mutation Gene Deletion Glycine-tRNA Ligase Homozygote Neuromuscular Junction Diseases RNA Splicing Action Potentials Neural Conduction Cells, Cultured Time Factors Arthrogryposis Immunohistochemistry Spinal Nerve Roots Optic Atrophy Fasciculation Gene Dosage Bulbar Palsy, Progressive Synapses Molecular Sequence Data Mice, Knockout Animals, Newborn Charcot-Marie-Tooth Disease Spinal Nerves Genes, Dominant Contracture RNA, Messenger Spliceosomes Injections, Spinal Genes, Recessive Muscles Ganglia, Spinal Alternative Splicing Muscle Weakness Chemistry, Analytic Mice, Inbred C57BL Genetic Linkage Prenatal Diagnosis Electric Stimulation Base Sequence Vocal Cord Paralysis Brain Survival Analysis Central Nervous System Hereditary Sensory and Motor Neuropathy Disease-Free Survival Genetic Counseling Growth Cones Neurites Respiratory Paralysis Fibroblasts Gene Expression Regulation Valproic Acid Mutation, Missense Survival Genetic Testing Multiple System Atrophy

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