Mutations and polymorphisms. Medical search. Frequent questions

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Anatomy6

Cell Line X Chromosome COS Cells Cells, Cultured Cell Line, Tumor HEK293 Cells

Organisms10

Escherichia coli Saccharomyces cerevisiae Drosophila melanogaster Drosophila Mice, Mutant Strains Cercopithecus aethiops Cricetinae HIV-1 Mice, Transgenic Mice, Inbred C57BL

Diseases17

Genetic Predisposition to Disease Syndrome Colorectal Neoplasms Breast Neoplasms Lung Neoplasms Retinitis Pigmentosa Genetic Diseases, X-Linked Chromosome Deletion Abnormalities, Multiple Adenocarcinoma Genetic Diseases, Inborn Diabetes Mellitus, Type 2 Disease Progression Neoplasms Ovarian Neoplasms Eye Abnormalities Disease Susceptibility

Chemicals and Drugs70

DNA Primers Genetic Markers Codon DNA Codon, Nonsense Methylenetetrahydrofolate Reductase (NADPH2)DNA-Binding Proteins Transcription Factors DNA, Mitochondrial Membrane Proteins DNA, Neoplasm Glutathione Transferase Carrier Proteins Bacterial Proteins DNA, Bacterial RNA, Messenger Nuclear Proteins Mutant Proteins Peptidyl-Dipeptidase A Deoxyribonucleases, Type II Site-Specific Catechol O-Methyltransferase DNA Transposable Elements Proteins Glutathione S-Transferase pi Valine Proto-Oncogene Proteins B-raf Recombinant Proteins Tumor Suppressor Protein p53 Aryl Hydrocarbon Hydroxylases Xeroderma Pigmentosum Group D Protein Eye Proteins DNA, Complementary Membrane Transport Proteins Serotonin Plasma Membrane Transport Proteins Proto-Oncogene Proteins Arginine RNA Splice Sites Mutagens Repressor Proteins Neoplasm Proteins BRCA2 Protein Alanine Ethylnitrosourea Saccharomyces cerevisiae Proteins Receptors, Calcitriol 3' Untranslated Regions Drosophila Proteins Arylamine N-Acetyltransferase Recombinant Fusion Proteins Nerve Tissue Proteins DNA, Plant ras Proteins Aryldialkylphosphatase Cytochrome P-450 CYP1A1 Tumor Suppressor Proteins Fungal Proteins Proline Codon, Terminator Glycine DNA, Fungal Escherichia coli Proteins 5' Untranslated Regions ATP-Binding Cassette Transporters Trans-Activators Cytosine Adaptor Proteins, Signal Transducing Protein-Serine-Threonine Kinases 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase DNA Probes Homeodomain Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment37

Polymerase Chain Reaction Pedigree Case-Control Studies Sequence Analysis, DNA Amino Acid Substitution DNA Mutational Analysis Genetic Association Studies Chromosome Mapping Genetic Testing Mutagenesis, Site-Directed Models, Genetic Risk Factors Sequence Alignment Heterozygote Detection Amplified Fragment Length Polymorphism Analysis Models, Molecular Cloning, Molecular Genome-Wide Association Study Odds Ratio Cohort Studies Genetic Complementation Test Mutagenesis, Insertional Transfection Crosses, Genetic Restriction Mapping Reverse Transcriptase Polymerase Chain Reaction Risk Genotyping Techniques Blotting, Southern Prognosis DNA Fingerprinting Chi-Square Distribution Logistic Models Models, Biological Immunohistochemistry Blotting, Western Oligonucleotide Array Sequence Analysis

Psychiatry and Psychology2

Phenomena and Processes108

Polymorphism, Genetic Polymorphism, Single Nucleotide Point Mutation Mutation, Missense Mutation Alleles Genetic Predisposition to Disease Gene Frequency Frameshift Mutation Genotype Polymorphism, Single-Stranded Conformational Germ-Line Mutation Base Sequence Heterozygote Haplotypes Exons Homozygote Amino Acid Substitution Genetic Variation Phenotype Mutation Rate Linkage Disequilibrium Amino Acid Sequence Genetic Markers Promoter Regions, Genetic Genetic Linkage Codon Microsatellite Repeats Codon, Nonsense Sequence Deletion Introns Genes, Recessive Mutagenesis Genes, Dominant Gene Deletion Genes, p53 INDEL Mutation Protein Structure, Tertiary Selection, Genetic Phylogeny Sequence Homology, Amino Acid Binding Sites Founder Effect Suppression, Genetic Evolution, Molecular Odds Ratio Mutagenesis, Insertional Recombination, Genetic Protein Binding Transfection Consanguinity Plasmids Transcription, Genetic Species Specificity Genes Genes, Bacterial Genes, BRCA1 DNA Repair Genetic Loci Genetic Heterogeneity DNA Transposable Elements Genome, Human Minisatellite Repeats Epistasis, Genetic Exome Genes, Lethal Risk Gene Expression Regulation Protein Conformation Conserved Sequence Signal Transduction Drug Resistance, Viral Tandem Repeat Sequences Gene Expression Penetrance X Chromosome Structure-Activity Relationship Sequence Homology, Nucleic Acid Kinetics Gene Dosage Drug Resistance Loss of Heterozygosity Genes, BRCA2 Dinucleotide Repeats RNA Splice Sites Biological Evolution Temperature RNA Splicing Repetitive Sequences, Nucleic Acid Genes, Suppressor Genes, Fungal Protein Structure, Secondary Chromosome Deletion 3' Untranslated Regions Time Factors Multigene Family Polymorphism, Restriction Fragment Length Chi-Square Distribution Quantitative Trait Loci Codon, Terminator Alternative Splicing 5' Untranslated Regions Drug Resistance, Microbial Mosaicism Genes, Insect Disease Susceptibility Open Reading Frames Genes, Plant

Disciplines and Occupations3

Genetics, Population Pharmacogenetics Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena2

DNA Fingerprinting Family

Information Science5

Base Sequence Molecular Sequence Data Amino Acid Sequence Phylogeny Publication Bias

Named Groups5

Asian Continental Ancestry Group European Continental Ancestry Group Jews Ethnic Groups Infant, Newborn

Health Care13

Case-Control Studies Genetic Testing Risk Factors Age of Onset Genome-Wide Association Study Odds Ratio Cohort Studies Family Health Risk Temperature Ethnic Groups Chi-Square Distribution Logistic Models

Geographicals8

China Japan Korea India Italy Tunisia Poland Spain

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 Named Groups Health Care Geographicals

Polymorphism, Genetic Polymorphism, Single Nucleotide Point Mutation Mutation, Missense Mutation Alleles Genetic Predisposition to Disease Gene Frequency Frameshift Mutation Polymerase Chain Reaction Genotype Polymorphism, Single-Stranded Conformational Germ-Line Mutation Base Sequence Pedigree Case-Control Studies Molecular Sequence Data Heterozygote Haplotypes Exons Sequence Analysis, DNA Homozygote Amino Acid Substitution Genetic Variation DNA Mutational Analysis Genetic Association Studies Asian Continental Ancestry Group Phenotype Mutation Rate Linkage Disequilibrium DNA Primers Chromosome Mapping Amino Acid Sequence Genetic Markers Promoter Regions, Genetic Genetic Linkage Codon Genetic Testing DNA Mutagenesis, Site-Directed Microsatellite Repeats Codon, Nonsense Models, Genetic Risk Factors Sequence Deletion Introns China Genes, Recessive Mutagenesis European Continental Ancestry Group Methylenetetrahydrofolate Reductase (NADPH2)Genes, Dominant DNA-Binding Proteins Gene Deletion Genes, p53 INDEL Mutation Sequence Alignment Protein Structure, Tertiary Heterozygote Detection Amplified Fragment Length Polymorphism Analysis Selection, Genetic Cell Line Phylogeny Models, Molecular Escherichia coli Genetics, Population Cloning, Molecular Sequence Homology, Amino Acid Transcription Factors Binding Sites DNA, Mitochondrial Founder Effect Age of Onset Suppression, Genetic Evolution, Molecular Membrane Proteins Genome-Wide Association Study Japan DNA, Neoplasm Odds Ratio Cohort Studies Syndrome Glutathione Transferase Carrier Proteins Genetic Complementation Test Mutagenesis, Insertional Recombination, Genetic Bacterial Proteins Protein Binding Family Health DNA, Bacterial RNA, Messenger Nuclear Proteins Transfection Consanguinity Plasmids Transcription, Genetic Mutant Proteins Species Specificity Genes

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