Genetic risk mutations. Medical search. Frequent questions

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Anatomy9

Cell Line Brain COS Cells Cells, Cultured Chromosomes, Human, Pair 10 Chromosomes, Human, Pair 17 X Chromosome Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 1

Organisms8

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

Diseases23

Genetic Predisposition to Disease Diseases in Twins Alzheimer Disease Genetic Diseases, Inborn Syndrome Breast Neoplasms Diabetes Mellitus, Type 2 Ovarian Neoplasms Thrombophilia Genetic Diseases, X-Linked Neoplastic Syndromes, Hereditary Retinitis Pigmentosa Macular Degeneration Disease Models, Animal Abnormalities, Multiple Colorectal Neoplasms Activated Protein C Resistance Disease Progression Eye Abnormalities Parkinson Disease Diabetes Mellitus, Type 1 Chromosome Aberrations Neoplasms

Chemicals and Drugs59

Apolipoprotein E4 Codon, Nonsense Genetic Markers DNA Primers Factor V DNA-Binding Proteins DNA Membrane Proteins Transcription Factors Codon HLA-DRB1 Chains Apolipoproteins E Mutant Proteins HLA-DQ Antigens Carrier Proteins Bacterial Proteins RNA, Messenger Nuclear Proteins Proteins DNA, Mitochondrial HLA-DQ beta-Chains Proto-Oncogene Proteins B-raf BRCA2 Protein Methylenetetrahydrofolate Reductase (NADPH2)Apolipoprotein E3 DNA, Neoplasm Prothrombin Recombinant Proteins Nerve Tissue Proteins Eye Proteins Oxidoreductases Acting on CH-NH Group Donors Mutagens Proto-Oncogene Proteins HLA-DR Antigens Saccharomyces cerevisiae Proteins Glucosylceramidase Ethylnitrosourea Protein Tyrosine Phosphatase, Non-Receptor Type 22 RNA Splice Sites Recombinant Fusion Proteins Adaptor Proteins, Signal Transducing Tumor Suppressor Protein p53 Transcription Factor 7-Like 2 Protein Repressor Proteins Fungal Proteins ras Proteins Escherichia coli Proteins DNA, Complementary Drosophila Proteins DNA, Bacterial HLA-DQ alpha-Chains DNA Transposable Elements HLA-DR3 Antigen HLA-DRB4 Chains HLA-B15 Antigen Trans-Activators Codon, Terminator Ethyl Methanesulfonate Presenilin-1

Analytical, Diagnostic and Therapeutic Techniques and Equipment39

Pedigree Genetic Testing Genome-Wide Association Study Risk Factors Polymerase Chain Reaction Case-Control Studies Amino Acid Substitution DNA Mutational Analysis Genetic Association Studies Sequence Analysis, DNA Mutagenesis, Site-Directed Heterozygote Detection Models, Genetic Chromosome Mapping Risk Cohort Studies Models, Molecular Risk Assessment Genetic Complementation Test Cloning, Molecular Sequence Alignment Transfection Odds Ratio Mutagenesis, Insertional Genotyping Techniques Crosses, Genetic Reverse Transcriptase Polymerase Chain Reaction Magnetic Resonance Imaging Disease Models, Animal Restriction Mapping Prospective Studies Abortion, Eugenic Prevalence ROC Curve Logistic Models Blotting, Western Prognosis Models, Biological Immunohistochemistry

Psychiatry and Psychology8

Family Alzheimer Disease Schizophrenia Siblings Neuropsychological Tests Nuclear Family Bipolar Disorder Reproductive Behavior

Phenomena and Processes105

Point Mutation Mutation, Missense Mutation Genetic Predisposition to Disease Frameshift Mutation Genotype Polymorphism, Single Nucleotide Germ-Line Mutation Alleles Heterozygote Mutation Rate Gene Frequency Exons Base Sequence Amino Acid Substitution Phenotype Polymorphism, Genetic Homozygote Genetic Variation Genetic Loci Polymorphism, Single-Stranded Conformational Genes, Recessive Amino Acid Sequence Codon, Nonsense Mutagenesis Genetic Linkage Gene-Environment Interaction Genes, Dominant Genetic Markers Genes, BRCA1 Sequence Deletion Linkage Disequilibrium Haplotypes Risk Genes, BRCA2 Protein Structure, Tertiary Gene Deletion Suppression, Genetic Codon Endophenotypes Penetrance Binding Sites Sequence Homology, Amino Acid Genome, Human Founder Effect Promoter Regions, Genetic Genes, p53 Protein Binding Multifactorial Inheritance Introns Consanguinity Plasmids Polymorphism, Restriction Fragment Length Transfection Genetic Heterogeneity Epistasis, Genetic Microsatellite Repeats Genes, Lethal Exome Odds Ratio Mutagenesis, Insertional Transcription, Genetic Signal Transduction Genes, Bacterial Protein Conformation Genetic Load Recombination, Genetic Structure-Activity Relationship Drug Resistance, Viral Genes Gene Expression Genes, Suppressor Kinetics Gene Expression Regulation Conserved Sequence INDEL Mutation Gene Dosage Temperature RNA Splicing RNA Splice Sites Selection, Genetic Genes, Fungal Evolution, Molecular Inheritance Patterns Time Factors Protein Structure, Secondary DNA Repair Chromosomes, Human, Pair 10 Environment Lod Score DNA Transposable Elements Chromosomes, Human, Pair 17 Reproductive Behavior Drug Resistance, Microbial Amino Acid Motifs Pregnancy Phosphorylation Loss of Heterozygosity X Chromosome Codon, Terminator Mosaicism Chromosome Aberrations Gene Expression Regulation, Bacterial Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 1

Disciplines and Occupations3

Genetic Counseling Genetics, Population Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena5

Family Siblings Adoption Social Environment Nuclear Family

Information Science4

Base Sequence Molecular Sequence Data Amino Acid Sequence Prevalence

Named Groups10

Asian Continental Ancestry Group European Continental Ancestry Group Twins, Monozygotic Twins, Dizygotic Siblings Infant, Newborn Jews Twins African Americans Child of Impaired Parents

Health Care18

Genetic Testing Genetic Counseling Genome-Wide Association Study Risk Factors Case-Control Studies Family Health Age of Onset Risk Cohort Studies Risk Assessment Odds Ratio Temperature Prospective Studies Prevalence Environment Genetic Services ROC Curve Logistic Models

Geographicals4

Japan China Finland Italy

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

Point Mutation Mutation, Missense Mutation Genetic Predisposition to Disease Frameshift Mutation Genotype Polymorphism, Single Nucleotide Germ-Line Mutation Alleles Pedigree Genetic Testing Heterozygote Genetic Counseling Genome-Wide Association Study Risk Factors Mutation Rate Gene Frequency Exons Base Sequence Polymerase Chain Reaction Case-Control Studies Amino Acid Substitution Phenotype Polymorphism, Genetic DNA Mutational Analysis Homozygote Molecular Sequence Data Apolipoprotein E4 Family Health Genetic Variation Genetic Loci Genetic Association Studies Polymorphism, Single-Stranded Conformational Sequence Analysis, DNA Mutagenesis, Site-Directed Heterozygote Detection Models, Genetic Genes, Recessive Amino Acid Sequence Codon, Nonsense Mutagenesis Age of Onset Genetic Linkage Chromosome Mapping Asian Continental Ancestry Group Gene-Environment Interaction Genes, Dominant Genetic Markers Genes, BRCA1 Diseases in Twins DNA Primers Factor V Sequence Deletion Linkage Disequilibrium Haplotypes Risk Genes, BRCA2 Protein Structure, Tertiary Cohort Studies DNA-Binding Proteins Gene Deletion Escherichia coli Suppression, Genetic Family Alzheimer Disease DNA Models, Molecular Membrane Proteins European Continental Ancestry Group Transcription Factors Schizophrenia Codon Risk Assessment HLA-DRB1 Chains Endophenotypes Cell Line Penetrance Binding Sites Genetic Diseases, Inborn Sequence Homology, Amino Acid Genetic Complementation Test Genome, Human Apolipoproteins E Founder Effect Promoter Regions, Genetic Genes, p53 Syndrome Cloning, Molecular Protein Binding Sequence Alignment Mutant Proteins HLA-DQ Antigens Multifactorial Inheritance Introns Twins, Monozygotic Saccharomyces cerevisiae Consanguinity Carrier Proteins Bacterial Proteins Plasmids

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