Recessive mutation disease models animal. Medical search. Frequent questions

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Anatomy9

Cell Line Cells, Cultured Chromosomes Plant Leaves Fibroblasts Brain Muscle, Skeletal X Chromosome Neurons

Organisms17

Mice, Mutant Strains Saccharomyces cerevisiae Mice, Inbred C57BL Mice, Neurologic Mutants Arabidopsis Drosophila melanogaster Zebrafish Mice, Inbred C3H Mice, Transgenic Mice, Knockout Escherichia coli Mice, Inbred Strains Zea mays Animals, Genetically Modified Drosophila Mice, Inbred BALB C Cricetinae

Diseases24

Disease Models, Animal Syndrome Hypotrichosis Genetic Diseases, Inborn Abnormalities, Multiple Deafness Genetic Predisposition to Disease Hereditary Central Nervous System Demyelinating Diseases Hearing Loss, Sensorineural Hearing Loss Retinitis Pigmentosa Chromosome Deletion Polycystic Kidney, Autosomal Recessive Huntington Disease Neurodegenerative Diseases Parkinson Disease Parkinsonian Disorders Ichthyosis Microcephaly Genetic Diseases, X-Linked Osteochondrodysplasias Intellectual Disability Eye Abnormalities Alzheimer Disease

Chemicals and Drugs31

Ethylnitrosourea Codon, Nonsense Ethyl Methanesulfonate DNA Primers Membrane Proteins RNA, Messenger Transcription Factors Genetic Markers Mutagens DNA-Binding Proteins Fungal Proteins DNA Eye Proteins Saccharomyces cerevisiae Proteins beta-Fructofuranosidase Carrier Proteins Arabidopsis Proteins Proteins Plant Proteins Codon DNA Transposable Elements Nuclear Proteins Repressor Proteins Nerve Tissue Proteins Mutant Proteins DNA, Fungal Recombinant Proteins Bacterial Proteins DNA, Mitochondrial RNA Splice Sites Recombinant Fusion Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment31

Animal Use Alternatives Disease Models, Animal Models, Animal Pedigree Chromosome Mapping DNA Mutational Analysis Crosses, Genetic Genetic Complementation Test Amino Acid Substitution Models, Genetic Polymerase Chain Reaction Sequence Analysis, DNA Genetic Testing Cloning, Molecular Sequence Alignment Mutagenesis, Site-Directed Inbreeding Mutagenesis, Insertional Models, Biological Heterozygote Detection Restriction Mapping Models, Molecular Blotting, Southern Transfection Reverse Transcriptase Polymerase Chain Reaction Microscopy, Electron, Scanning Microscopy, Electron Immunohistochemistry In Situ Hybridization Blotting, Western Gene Targeting

Psychiatry and Psychology3

Huntington Disease Intellectual Disability Alzheimer Disease

Phenomena and Processes79

Genes, Recessive Mutation Mutation, Missense Point Mutation Homozygote Phenotype Frameshift Mutation Alleles Heterozygote Consanguinity Base Sequence Genes, Dominant Mutagenesis Genetic Load Amino Acid Sequence Codon, Nonsense Genetic Linkage Genotype Exons Germ-Line Mutation Genes, Lethal Exome Amino Acid Substitution Genes, Fungal Suppression, Genetic Sequence Deletion Mutation Rate Genes, Plant Genetic Predisposition to Disease Sequence Homology, Amino Acid Gene Deletion Polymorphism, Single-Stranded Conformational Diploidy Epistasis, Genetic Genetic Markers Microsatellite Repeats Polymorphism, Single Nucleotide Recombination, Genetic Genes Inbreeding Mutagenesis, Insertional Polymorphism, Genetic Signal Transduction Gene Expression Regulation Transcription, Genetic Gene Expression Haplotypes Founder Effect Haploidy Plasmids Chromosomes Gene Expression Regulation, Plant Protein Structure, Tertiary Genes, Regulator Temperature Chromosome Deletion Protein Binding Codon DNA Transposable Elements Gene Expression Regulation, Developmental Gene Expression Regulation, Fungal Gene Frequency Genetic Variation Binding Sites Lod Score Transfection Morphogenesis Genetic Heterogeneity Genes, p53 Introns Sequence Homology, Nucleic Acid Reproduction Meiosis X Chromosome Penetrance Genes, Suppressor RNA Splice Sites Polymorphism, Restriction Fragment Length Promoter Regions, Genetic

Disciplines and Occupations1

Immunohistochemistry

Technology, Industry, Agriculture1

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Computer Simulation

Named Groups2

Infant, Newborn Jews

Health Care4

Genetic Testing Temperature Family Health 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 Technology, Industry, Agriculture Information Science Named Groups Health Care

Animal Use Alternatives Genes, Recessive Disease Models, Animal Models, Animal Mutation Mutation, Missense Point Mutation Homozygote Pedigree Phenotype Chromosome Mapping Frameshift Mutation Ethylnitrosourea Alleles Heterozygote Consanguinity Molecular Sequence Data DNA Mutational Analysis Base Sequence Genes, Dominant Crosses, Genetic Mutagenesis Genetic Load Mice, Mutant Strains Amino Acid Sequence Genetic Complementation Test Codon, Nonsense Genetic Linkage Genotype Exons Germ-Line Mutation Genes, Lethal Syndrome Hypotrichosis Exome Amino Acid Substitution Models, Genetic Saccharomyces cerevisiae Genetic Diseases, Inborn Genes, Fungal Polymerase Chain Reaction Ethyl Methanesulfonate Suppression, Genetic Sequence Analysis, DNA Abnormalities, Multiple Mice, Inbred C57BL Genetic Testing Sequence Deletion Mutation Rate Deafness Genes, Plant DNA Primers Genetic Predisposition to Disease Membrane Proteins Cloning, Molecular Mice, Neurologic Mutants Sequence Homology, Amino Acid Gene Deletion Arabidopsis Polymorphism, Single-Stranded Conformational Diploidy Epistasis, Genetic Hereditary Central Nervous System Demyelinating Diseases RNA, Messenger Transcription Factors Genetic Markers Cell Line Mutagens Sequence Alignment Drosophila melanogaster DNA-Binding Proteins Microsatellite Repeats Polymorphism, Single Nucleotide Fungal Proteins Hearing Loss, Sensorineural Zebrafish Mutagenesis, Site-Directed Recombination, Genetic DNA Genes Eye Proteins Mice, Inbred C3H Inbreeding Saccharomyces cerevisiae Proteins Mutagenesis, Insertional Polymorphism, Genetic Models, Biological Cells, Cultured Hearing Loss Signal Transduction Gene Expression Regulation Mice, Transgenic Transcription, Genetic Gene Expression Retinitis Pigmentosa Haplotypes beta-Fructofuranosidase Founder Effect Haploidy Plasmids

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