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Anatomy15

Mitochondria X Chromosome Cell Membrane Chromosomes, Human, X Liver Cell Line Nose Intracellular Membranes Cells, Cultured Erythrocytes Mitochondria, Liver Nasal Cavity Brain trans-Golgi Network Pharynx

Organisms9

Escherichia coli Hepatitis B virus Cattle Rabbits Neisseria meningitidis Staphylococcus aureus Human T-lymphotropic virus 1 Mice, Inbred BALB C Saccharomyces cerevisiae

Diseases22

Genetic Predisposition to Disease Tay-Sachs Disease Hepatitis B Fragile X Syndrome Breast Neoplasms Ovarian Neoplasms Muscular Dystrophies HTLV-I Infections Hepatitis B, Chronic Colorectal Neoplasms, Hereditary Nonpolyposis Translocation, Genetic Genetic Diseases, X-Linked Cystic Fibrosis Hemophilia A Ataxia Tremor Paraparesis, Tropical Spastic Staphylococcal Infections Sex Chromosome Aberrations Leukemia L1210 Asymptomatic Infections Intellectual Disability

Chemicals and Drugs104

Drug Carriers Carrier Proteins Acyl Carrier Protein Reduced Folate Carrier Protein Mitochondrial ADP, ATP Translocases Membrane Transport Proteins BRCA2 Protein Blood Substitutes Fatty Acid Synthase, Type II Melibiose Pantetheine Liposomes Symporters Hepatitis B Surface Antigens 3-Oxoacyl-(Acyl-Carrier-Protein) Synthase BRCA1 Protein Haptens Apolipoprotein E4 Fragile X Mental Retardation Protein Membrane Proteins Dicarboxylic Acid Transporters Mitochondrial Proteins Polymers Acyl-Carrier Protein S-Malonyltransferase Bacterial Proteins Polyethylene Glycols Nanocapsules Hepatitis B Antigens Chitosan Enoyl-(Acyl-Carrier-Protein) Reductase (NADH)DNA Atractyloside Lactose DNA Primers Fatty Acids Amino Acid Transport Systems, Neutral Mitochondrial Membrane Transport Proteins Hepatitis B e Antigens Hepatitis B Antibodies Powders Recombinant Proteins Polyethyleneimine 3-Oxoacyl-(Acyl-Carrier-Protein) Reductase Folate Receptors, GPI-Anchored Lipids Transferases (Other Substituted Phosphate Groups)Dinitrophenols Sodium Polyketide Synthases Acyltransferases Hemocyanin Mersalyl Monosaccharide Transport Proteins Factor V Escherichia coli Proteins Galactosides Genetic Markers Micelles Amino Acid Transport Systems, Acidic Delayed-Action Preparations Dendrimers Hexosaminidase A Emulsions Serum Albumin, Bovine Folic Acid Antagonists Folic Acid Triclosan Coenzyme A Peptides Proton-Coupled Folate Transporter Methotrexate Apolipoproteins E 4-Chloromercuribenzenesulfonate MutS Homolog 2 Protein Fatty Acid Synthases Carbon-Sulfur Ligases Acetyl-CoA C-Acetyltransferase RNA, Messenger Ethylmaleimide Proteolipids Recombinant Fusion Proteins Pharmaceutical Vehicles Polyglutamic Acid Nucleotide Transport Proteins Hepatitis B Core Antigens Biotin Methylglycosides DNA, Viral Sulfhydryl Reagents Hemoglobins Proline Epitopes Antiporters Indoleacetic Acids beta-N-Acetylhexosaminidases Hemoglobins, Abnormal Organic Anion Transporters gamma-Globulins Vaccines, Conjugate Immunoglobulin G Serotonin Plasma Membrane Transport Proteins Peptide Synthases Cell-Penetrating Peptides Methylglucosides

Analytical, Diagnostic and Therapeutic Techniques and Equipment36

Drug Carriers Heterozygote Detection Genetic Testing Pedigree DNA Mutational Analysis Drug Delivery Systems Polymerase Chain Reaction Case-Control Studies Prenatal Diagnosis Risk Factors Drug Compounding Nanocapsules Genetic Association Studies Cloning, Molecular Cohort Studies Salpingectomy Risk Technology, Pharmaceutical Models, Molecular Models, Biological Amino Acid Substitution Sequence Analysis, DNA Preimplantation Diagnosis Delayed-Action Preparations Dendrimers Prevalence Neonatal Screening Pharmaceutical Vehicles Color Perception Tests Drug Stability Transfection Electrophoresis, Polyacrylamide Gel Sequence Alignment Odds Ratio Immunization Microspheres

Psychiatry and Psychology1

Intellectual Disability

Phenomena and Processes64

Heterozygote Mutation Genes, BRCA1 Genotype Genes, BRCA2 Genetic Predisposition to Disease Polymorphism, Genetic Alleles Biological Transport Germ-Line Mutation Polymorphism, Single Nucleotide Gene Frequency Amino Acid Sequence Kinetics Penetrance Phenotype Homozygote Base Sequence Particle Size Haplotypes Founder Effect Biological Transport, Active Genetic Variation X Chromosome Hydrogen-Ion Concentration Genetic Linkage Time Factors Mutation, Missense Point Mutation Polymorphism, Restriction Fragment Length Genes, Recessive Solubility Exons Risk Pregnancy Chromosomes, Human, X Sequence Homology, Amino Acid Substrate Specificity Amino Acid Substitution Translocation, Genetic Protein Binding Protein Conformation Antibody Formation Genetic Markers Dosage Compensation, Genetic Gene Deletion Binding Sites Protein Transport Tissue Distribution Plasmids Sex Chromosome Aberrations Polymorphism, Single-Stranded Conformational Transfection Protein Structure, Tertiary Temperature Oxidation-Reduction Trinucleotide Repeat Expansion X Chromosome Inactivation Molecular Weight Sequence Deletion DNA Mismatch Repair Odds Ratio Structure-Activity Relationship Gene Expression

Disciplines and Occupations5

Genetic Counseling Chemistry, Pharmaceutical Technology, Pharmaceutical Nanomedicine Nanotechnology

Technology, Industry, Agriculture12

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

Information Science4

Molecular Sequence Data Amino Acid Sequence Base Sequence Prevalence

Named Groups3

Jews Infant, Newborn Asian Continental Ancestry Group

Health Care16

Carrier State Genetic Testing Genetic Counseling Case-Control Studies Risk Factors Family Health Age of Onset Cohort Studies Insurance Carriers Risk Prevalence Neonatal Screening Age Factors Temperature Odds Ratio Immunization

Geographicals1

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 Genes, BRCA1 Genotype Genetic Testing Genes, BRCA2 Pedigree Mitochondrial ADP, ATP Translocases Genetic Predisposition to Disease Membrane Transport Proteins Polymorphism, Genetic Alleles Biological Transport Jews Molecular Sequence Data Germ-Line Mutation Genetic Counseling BRCA2 Protein Polymorphism, Single Nucleotide Blood Substitutes Gene Frequency Amino Acid Sequence Kinetics Penetrance DNA Mutational Analysis Drug Delivery Systems Polymerase Chain Reaction Phenotype Homozygote Fatty Acid Synthase, Type II Base Sequence Tay-Sachs Disease Case-Control Studies Melibiose Pantetheine Hepatitis B Liposomes Symporters Hepatitis B Surface Antigens 3-Oxoacyl-(Acyl-Carrier-Protein) Synthase BRCA1 Protein Fragile X Syndrome Nanoparticles Particle Size Prenatal Diagnosis Haptens Escherichia coli Apolipoprotein E4 Haplotypes Breast Neoplasms Founder Effect Risk Factors Biological Transport, Active Fragile X Mental Retardation Protein Family Health Mitochondria Genetic Variation X Chromosome Hydrogen-Ion Concentration Membrane Proteins Drug Compounding Genetic Linkage Hepatitis B virus Dicarboxylic Acid Transporters Ovarian Neoplasms Mitochondrial Proteins Polymers Chemistry, Pharmaceutical Acyl-Carrier Protein S-Malonyltransferase Age of Onset Muscular Dystrophies Bacterial Proteins Polyethylene Glycols Time Factors Nanocapsules Cell Membrane Mutation, Missense HTLV-I Infections Hepatitis B Antigens Point Mutation Chitosan Genetic Association Studies Enoyl-(Acyl-Carrier-Protein) Reductase (NADH)Hepatitis B, Chronic DNA Atractyloside Cloning, Molecular Polymorphism, Restriction Fragment Length Lactose Genes, Recessive Cohort Studies Solubility Cattle DNA Primers

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