Peripheral mutation disease models animal. Medical search. Frequent questions

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Anatomy10

Peripheral Nerves Peripheral Nervous System Cells, Cultured Cell Line Leukocytes, Mononuclear T-Lymphocytes Neurons Brain Lymphocytes B-Lymphocytes

Organisms12

Mice, Inbred C57BL Mice, Transgenic Mice, Knockout Escherichia coli Mice, Mutant Strains Mice, Inbred BALB C Animals, Genetically Modified Saccharomyces cerevisiae Drosophila melanogaster Cricetinae Drosophila Rats, Sprague-Dawley

Diseases15

Disease Models, Animal Peripheral Nervous System Diseases Peripheral Vascular Diseases Genetic Predisposition to Disease Peripheral Nerve Injuries Peripheral Arterial Disease Genetic Diseases, Inborn Huntington Disease Neurodegenerative Diseases Syndrome Parkinson Disease Lymphoma, T-Cell, Peripheral Alzheimer Disease Parkinsonian Disorders Inflammation

Chemicals and Drugs21

Codon, Nonsense DNA Primers RNA, Messenger Membrane Proteins DNA-Binding Proteins Transcription Factors Recombinant Proteins Ethylnitrosourea Codon Nuclear Proteins DNA Nerve Tissue Proteins Mutant Proteins Bacterial Proteins Genetic Markers Cytokines Carrier Proteins Recombinant Fusion Proteins DNA, Mitochondrial Neuroprotective Agents DNA, Neoplasm

Analytical, Diagnostic and Therapeutic Techniques and Equipment27

Animal Use Alternatives Disease Models, Animal Models, Animal Pedigree Polymerase Chain Reaction Amino Acid Substitution DNA Mutational Analysis Sequence Analysis, DNA Mutagenesis, Site-Directed Chromosome Mapping Models, Genetic Genetic Testing Reverse Transcriptase Polymerase Chain Reaction Models, Biological Models, Molecular Immunohistochemistry Transfection Cloning, Molecular Lymphocyte Activation Genetic Complementation Test Sequence Alignment Flow Cytometry Blotting, Western Case-Control Studies Heterozygote Detection Gene Expression Profiling Gene Targeting

Psychiatry and Psychology2

Huntington Disease Alzheimer Disease

Phenomena and Processes50

Point Mutation Mutation, Missense Mutation Frameshift Mutation Germ-Line Mutation Base Sequence Mutation Rate Exons Alleles Heterozygote Amino Acid Sequence Amino Acid Substitution Phenotype Genotype Polymorphism, Single-Stranded Conformational Mutagenesis Homozygote Codon, Nonsense Genetic Predisposition to Disease Genes, Recessive Signal Transduction Genetic Linkage Gene Deletion Sequence Deletion Time Factors Genes, Dominant Protein Structure, Tertiary Protein Binding Gene Expression Regulation Suppression, Genetic Binding Sites Sequence Homology, Amino Acid Gene Expression Codon Transfection Lymphocyte Activation Cell Differentiation Polymorphism, Single Nucleotide Genetic Variation Genes, p53 Founder Effect Genetic Markers Plasmids Consanguinity Transcription, Genetic Polymorphism, Genetic Epistasis, Genetic Kinetics Genes, Lethal Promoter Regions, Genetic

Disciplines and Occupations1

Immunohistochemistry

Information Science4

Base Sequence Molecular Sequence Data Amino Acid Sequence Computer Simulation

Health Care3

Genetic Testing Case-Control Studies Family Health

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

Animal Use Alternatives Disease Models, Animal Models, Animal Point Mutation Mutation, Missense Mutation Frameshift Mutation Germ-Line Mutation Peripheral Nerves Pedigree Base Sequence Molecular Sequence Data Polymerase Chain Reaction Mutation Rate Exons Alleles Heterozygote Amino Acid Sequence Mice, Inbred C57BL Peripheral Nervous System Amino Acid Substitution Phenotype Peripheral Nervous System Diseases DNA Mutational Analysis Genotype Cells, Cultured Polymorphism, Single-Stranded Conformational Mice, Transgenic Cell Line Mutagenesis Sequence Analysis, DNA Mutagenesis, Site-Directed Peripheral Vascular Diseases Chromosome Mapping Homozygote Models, Genetic Codon, Nonsense DNA Primers Mice, Knockout RNA, Messenger Genetic Predisposition to Disease Genes, Recessive Leukocytes, Mononuclear Signal Transduction Genetic Linkage Gene Deletion Membrane Proteins DNA-Binding Proteins Sequence Deletion Time Factors Genes, Dominant Protein Structure, Tertiary Genetic Testing Protein Binding Transcription Factors Reverse Transcriptase Polymerase Chain Reaction Models, Biological T-Lymphocytes Escherichia coli Peripheral Nerve Injuries Gene Expression Regulation Models, Molecular Peripheral Arterial Disease Suppression, Genetic Genetic Diseases, Inborn Huntington Disease Binding Sites Sequence Homology, Amino Acid Immunohistochemistry Recombinant Proteins Ethylnitrosourea Gene Expression Codon Mice, Mutant Strains Neurons Brain Transfection Nuclear Proteins Neurodegenerative Diseases DNA Syndrome Cloning, Molecular Lymphocyte Activation Genetic Complementation Test Nerve Tissue Proteins Mice, Inbred BALB C Cell Differentiation Polymorphism, Single Nucleotide Sequence Alignment Genetic Variation Genes, p53 Founder Effect Lymphocytes Parkinson Disease Mutant Proteins Animals, Genetically Modified Lymphoma, T-Cell, Peripheral Bacterial Proteins Flow Cytometry Saccharomyces cerevisiae

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