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Anatomy15

X Chromosome Cell Line Mitochondria Cell Membrane Cells, Cultured Liver Chromosomes, Human, X Brain Intracellular Membranes Nose Erythrocytes Chromosomes, Bacterial HeLa Cells Cell Line, Tumor Nasal Cavity

Organisms9

Escherichia coli Hepatitis B virus Cattle Saccharomyces cerevisiae Rabbits Staphylococcus aureus Mice, Inbred BALB C Mice, Inbred C57BL Cricetinae

Diseases19

Genetic Predisposition to Disease Fragile X Syndrome Hepatitis B Tay-Sachs Disease Breast Neoplasms Ovarian Neoplasms Muscular Dystrophies Translocation, Genetic HTLV-I Infections Hepatitis B, Chronic Cystic Fibrosis Genetic Diseases, X-Linked Colorectal Neoplasms, Hereditary Nonpolyposis Staphylococcal Infections Ataxia Syndrome Hemophilia A Sex Chromosome Aberrations Chromosome Deletion

Chemicals and Drugs81

Drug Carriers Carrier Proteins Acyl Carrier Protein Reduced Folate Carrier Protein Membrane Transport Proteins Mitochondrial ADP, ATP Translocases BRCA2 Protein Bacterial Proteins Blood Substitutes Liposomes Symporters Fatty Acid Synthase, Type II BRCA1 Protein Melibiose Pantetheine Hepatitis B Surface Antigens Membrane Proteins DNA 3-Oxoacyl-(Acyl-Carrier-Protein) Synthase Haptens Apolipoprotein E4 DNA Primers DNA, Bacterial Fragile X Mental Retardation Protein Recombinant Proteins Escherichia coli Proteins Polymers Mitochondrial Proteins Genetic Markers RNA, Messenger Polyethylene Glycols Dicarboxylic Acid Transporters Lactose Recombinant Fusion Proteins Acyl-Carrier Protein S-Malonyltransferase DNA, Viral DNA Transposable Elements Nanocapsules Peptides Fatty Acids Hepatitis B Antigens Chitosan Enoyl-(Acyl-Carrier-Protein) Reductase (NADH)Atractyloside Epitopes DNA-Binding Proteins Lipids Anti-Bacterial Agents Proteins Acyltransferases Sodium Amino Acid Transport Systems, Neutral Mitochondrial Membrane Transport Proteins Transferases (Other Substituted Phosphate Groups)Hepatitis B e Antigens Monosaccharide Transport Proteins Hepatitis B Antibodies DNA, Complementary Galactosides Powders Plant Proteins Polyethyleneimine 3-Oxoacyl-(Acyl-Carrier-Protein) Reductase Factor V Transcription Factors Folate Receptors, GPI-Anchored Dinitrophenols Saccharomyces cerevisiae Proteins Nuclear Proteins Amino Acids Biotin Polyketide Synthases MutS Homolog 2 Protein Folic Acid Proline Hemocyanin Mersalyl Serum Albumin, Bovine Apolipoproteins E Immunoglobulin G Methotrexate

Analytical, Diagnostic and Therapeutic Techniques and Equipment45

Drug Carriers Heterozygote Detection Genetic Testing Pedigree Polymerase Chain Reaction DNA Mutational Analysis Case-Control Studies Drug Delivery Systems Cloning, Molecular Risk Factors Sequence Analysis, DNA Prenatal Diagnosis Chromosome Mapping Models, Molecular Models, Biological Sequence Alignment Amino Acid Substitution Drug Compounding Cohort Studies Genetic Association Studies Risk Genetic Complementation Test Nanocapsules Transfection Electrophoresis, Polyacrylamide Gel Blotting, Southern Models, Genetic Prevalence Preimplantation Diagnosis Salpingectomy Restriction Mapping In Situ Hybridization, Fluorescence Technology, Pharmaceutical Prospective Studies Reverse Transcriptase Polymerase Chain Reaction Mutagenesis, Insertional Chromatography, High Pressure Liquid Karyotyping Nucleic Acid Hybridization Magnetic Resonance Imaging Mutagenesis, Site-Directed Blotting, Western Sensitivity and Specificity Neonatal Screening Retrospective Studies

Psychiatry and Psychology1

Phenomena and Processes82

Heterozygote Mutation Genotype Genes, BRCA1 Genes, BRCA2 Alleles Base Sequence Genetic Predisposition to Disease Amino Acid Sequence Polymorphism, Genetic Biological Transport Phenotype Germ-Line Mutation Kinetics Polymorphism, Single Nucleotide Gene Frequency Homozygote Plasmids Penetrance Haplotypes Founder Effect Genetic Variation Time Factors Particle Size Genetic Linkage X Chromosome Sequence Homology, Amino Acid Genes, Bacterial Biological Transport, Active Point Mutation Mutation, Missense Hydrogen-Ion Concentration Genes, Recessive Protein Binding Exons Binding Sites Polymorphism, Restriction Fragment Length Amino Acid Substitution Pregnancy Gene Deletion Genetic Markers Phylogeny Protein Conformation Substrate Specificity Protein Structure, Tertiary Translocation, Genetic Sequence Deletion Risk Solubility DNA Transposable Elements Species Specificity Transfection Temperature Genes Multigene Family Molecular Weight Promoter Regions, Genetic Chromosomes, Human, X Gene Expression Protein Transport Recombination, Genetic Transcription, Genetic Structure-Activity Relationship Dosage Compensation, Genetic Genetic Vectors Oxidation-Reduction Tissue Distribution Antibody Formation Polymorphism, Single-Stranded Conformational Molecular Structure Gene Expression Regulation Chromosomes, Bacterial Mutagenesis, Insertional Conjugation, Genetic Genes, Dominant Introns Sex Chromosome Aberrations Nucleic Acid Hybridization Open Reading Frames Sensitivity and Specificity Chromosome Deletion Frameshift Mutation

Disciplines and Occupations4

Genetic Counseling Chemistry, Pharmaceutical Nanomedicine Technology, Pharmaceutical

Anthropology, Education, Sociology and Social Phenomena1

Technology, Industry, Agriculture10

Blood Substitutes Liposomes Nanoparticles Polymers Polyethylene Glycols Nanocapsules Nanomedicine Polyethyleneimine Technology, Pharmaceutical Nanostructures

Information Science5

Molecular Sequence Data Base Sequence Amino Acid Sequence Phylogeny Prevalence

Named Groups3

Jews Infant, Newborn Asian Continental Ancestry Group

Health Care17

Carrier State Genetic Testing Genetic Counseling Case-Control Studies Risk Factors Family Health Age of Onset Cohort Studies Risk Temperature Prevalence Insurance Carriers Age Factors Prospective Studies Sensitivity and Specificity Neonatal Screening Retrospective Studies

Geographicals2

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes Disciplines and Occupations Technology, Industry, Agriculture Information Science Named Groups Health Care

Carrier State Drug Carriers Carrier Proteins Acyl Carrier Protein Heterozygote Detection Heterozygote Reduced Folate Carrier Protein Mutation Molecular Sequence Data Genotype Genes, BRCA1 Genetic Testing Pedigree Genes, BRCA2 Alleles Base Sequence Genetic Predisposition to Disease Amino Acid Sequence Membrane Transport Proteins Polymorphism, Genetic Mitochondrial ADP, ATP Translocases Biological Transport Jews Escherichia coli Phenotype Germ-Line Mutation Polymerase Chain Reaction DNA Mutational Analysis Genetic Counseling Kinetics BRCA2 Protein Polymorphism, Single Nucleotide Gene Frequency Homozygote Plasmids Bacterial Proteins Penetrance Blood Substitutes Case-Control Studies Drug Delivery Systems Cloning, Molecular Haplotypes Risk Factors Founder Effect Liposomes Fragile X Syndrome Genetic Variation Symporters Fatty Acid Synthase, Type II Nanoparticles BRCA1 Protein Hepatitis B Tay-Sachs Disease Sequence Analysis, DNA Melibiose Pantetheine Hepatitis B Surface Antigens Prenatal Diagnosis Breast Neoplasms Time Factors Membrane Proteins DNA Particle Size 3-Oxoacyl-(Acyl-Carrier-Protein) Synthase Genetic Linkage Haptens Apolipoprotein E4 X Chromosome Sequence Homology, Amino Acid Genes, Bacterial Chromosome Mapping Biological Transport, Active Point Mutation DNA Primers Cell Line Mitochondria Family Health Mutation, Missense Hydrogen-Ion Concentration DNA, Bacterial Fragile X Mental Retardation Protein Models, Molecular Cell Membrane Models, Biological Genes, Recessive Recombinant Proteins Protein Binding Exons Ovarian Neoplasms Binding Sites Age of Onset Escherichia coli Proteins Polymorphism, Restriction Fragment Length Sequence Alignment Hepatitis B virus Cattle Amino Acid Substitution Pregnancy Gene Deletion Polymers

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