Enzyme activity homozygote. Medical search. Frequent questions

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Anatomy13

Liver Microsomes, Liver Cells, Cultured Brain Erythrocytes Cell Line Kidney Microsomes Lysosomes Fibroblasts Subcellular Fractions Cytosol Muscle, Skeletal

Organisms11

Mice, Mutant Strains Escherichia coli Rats, Inbred Strains Cattle Mice, Inbred C57BL Drosophila melanogaster Mice, Knockout Rabbits Mice, Inbred Strains Mice, Transgenic Rats, Wistar

Diseases20

Genetic Predisposition to Disease Hemochromatosis Albinism Hyperlipoproteinemia Type II Gaucher Disease Hyperlipoproteinemia Type III Ataxia Telangiectasia Xanthomatosis Thalassemia Metabolism, Inborn Errors alpha 1-Antitrypsin Deficiency Lipid Metabolism, Inborn Errors Wolman Disease Polycythemia Hypolipoproteinemias Body Weight alpha-Thalassemia Disease Models, Animal Embryo Loss Cystic Fibrosis

Chemicals and Drugs109

Enzymes Catechol O-Methyltransferase RNA, Messenger Oxidoreductases Isoenzymes Apolipoprotein E2 Methylenetetrahydrofolate Reductase (NADPH2)Peptidyl-Dipeptidase A Glucosephosphate Dehydrogenase Malate Dehydrogenase DNA Primers DNA Catalase Glutathione Peroxidase Oxidoreductases Acting on CH-NH Group Donors Membrane Proteins Lipase Acid Phosphatase Superoxide Dismutase Genetic Markers Cytochrome P-450 Enzyme System Aryl Hydrocarbon Hydroxylases L-Lactate Dehydrogenase Glutathione Transferase Glutathione Reductase Hexosaminidases Recombinant Proteins Glucuronosyltransferase Esterases Cholesterol Lipids Ferritins Ethylnitrosourea Valine Alkaline Phosphatase Iron Carboxy-Lyases Histocompatibility Antigens Class I Apolipoproteins E Arginine Phosphotransferases Aryldialkylphosphatase Mixed Function Oxygenases Phosphogluconate Dehydrogenase Proline Hemoglobin E beta-Glucosidase Methionine Nucleotidases Porphobilinogen Synthase Citrate (si)-Synthase Proteins Hydrolases Hemoglobins, Abnormal Glycoside Hydrolases Lipoprotein Lipase Codon Triglycerides Sucrase Apolipoproteins A Antioxidants Magnesium Cations, Divalent alpha-Glucosidases Glucosylceramidase Pyruvate Kinase Transferrin Alcohol Oxidoreductases Homocysteine Acetylglucosaminidase DNA, Complementary Cholinesterases Cysteine Serotonin Plasma Membrane Transport Proteins Glucose Enzyme Inhibitors Hexosaminidase B Amino Acids Acyltransferases Carrier Proteins Disaccharidases Glucuronidase Aspartate Aminotransferases Glucosidases Succinate Dehydrogenase beta-N-Acetylhexosaminidases NAD Lipoproteins Folic Acid Transferases Apolipoprotein E4 Apolipoprotein C-III Glutathione Cytochrome P-450 CYP1A1 Arylamine N-Acetyltransferase Cystathionine beta-Synthase Manganese Alcohol Dehydrogenase NADP Isocitrate Dehydrogenase Hydroxybutyrate Dehydrogenase Glucosyltransferases Alanine Ornithine Decarboxylase Apolipoprotein A-I Apolipoproteins B Deoxyribonucleases, Type II Site-Specific 3-Hydroxyacyl CoA Dehydrogenases Hexokinase

Analytical, Diagnostic and Therapeutic Techniques and Equipment37

Heterozygote Detection Case-Control Studies Polymerase Chain Reaction Pedigree Crosses, Genetic Enzyme Stability Amino Acid Substitution Electrophoresis, Polyacrylamide Gel Cloning, Molecular Genetic Association Studies Risk Factors DNA Mutational Analysis Genetic Testing Chromosome Mapping Chromatography, Gel Enzyme Assays Mutagenesis, Site-Directed Reference Values Models, Genetic Sequence Analysis, DNA Electrophoresis, Starch Gel Chromatography, Ion Exchange Blotting, Western Chromatography, High Pressure Liquid Organ Size Cohort Studies Sequence Alignment Odds Ratio Analysis of Variance Histocytochemistry Blotting, Southern Reverse Transcriptase Polymerase Chain Reaction Spectrophotometry Body Weight Chromatography Disease Models, Animal Risk

Phenomena and Processes66

Homozygote Heterozygote Genotype Polymorphism, Genetic Alleles Gene Frequency Mutation Genetic Predisposition to Disease Polymorphism, Single Nucleotide Phenotype Kinetics Base Sequence Amino Acid Sequence Genetic Variation Haplotypes Substrate Specificity Genes, Lethal Hydrogen-Ion Concentration Genes, Recessive Point Mutation Enzyme Induction Polymorphism, Restriction Fragment Length Enzyme Stability Amino Acid Substitution Temperature Molecular Weight Enzyme Activation Gene Expression Regulation, Enzymologic Mutation, Missense Time Factors Exons Linkage Disequilibrium Genes, Dominant Genes Promoter Regions, Genetic Genetic Markers Gene Expression Sequence Homology, Amino Acid Binding Sites Genetic Linkage Catalysis Hair Color Gene Deletion Hydrolysis Species Specificity Organ Size Oxidation-Reduction Codon Sequence Deletion Hot Temperature Oxidative Stress Aging Gene Expression Regulation Odds Ratio Dose-Response Relationship, Drug Protein Binding Pregnancy Eye Color Transcription, Genetic Introns Selection, Genetic Body Weight Risk Tissue Distribution Mutagenesis Structure-Activity Relationship

Disciplines and Occupations2

Genetics, Population Histocytochemistry

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups3

Asian Continental Ancestry Group European Continental Ancestry Group Jews

Health Care10

Case-Control Studies Temperature Risk Factors Genetic Testing Cohort Studies Hot Temperature Odds Ratio Analysis of Variance Age of Onset Risk

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

Homozygote Heterozygote Genotype Polymorphism, Genetic Alleles Gene Frequency Mutation Genetic Predisposition to Disease Polymorphism, Single Nucleotide Phenotype Hemochromatosis Kinetics Molecular Sequence Data Liver Base Sequence Amino Acid Sequence Genetic Variation Haplotypes Heterozygote Detection Case-Control Studies Substrate Specificity Enzymes Genes, Lethal Polymerase Chain Reaction Mice, Mutant Strains Catechol O-Methyltransferase Hydrogen-Ion Concentration RNA, Messenger Oxidoreductases Genes, Recessive Isoenzymes Point Mutation Enzyme Induction Apolipoprotein E2 Pedigree Methylenetetrahydrofolate Reductase (NADPH2)Peptidyl-Dipeptidase A Polymorphism, Restriction Fragment Length Crosses, Genetic Glucosephosphate Dehydrogenase Albinism Malate Dehydrogenase Hyperlipoproteinemia Type II Enzyme Stability DNA Primers Amino Acid Substitution Electrophoresis, Polyacrylamide Gel DNA Cloning, Molecular Temperature Genetic Association Studies Catalase Molecular Weight Enzyme Activation Glutathione Peroxidase Risk Factors Gene Expression Regulation, Enzymologic Oxidoreductases Acting on CH-NH Group Donors Escherichia coli Asian Continental Ancestry Group DNA Mutational Analysis Gaucher Disease Mutation, Missense Time Factors Genetic Testing Exons Membrane Proteins Chromosome Mapping Lipase Microsomes, Liver Linkage Disequilibrium Cells, Cultured European Continental Ancestry Group Acid Phosphatase Superoxide Dismutase Genes, Dominant Genes Promoter Regions, Genetic Genetic Markers Gene Expression Sequence Homology, Amino Acid Rats, Inbred Strains Cytochrome P-450 Enzyme System Aryl Hydrocarbon Hydroxylases Cattle L-Lactate Dehydrogenase Chromatography, Gel Binding Sites Enzyme Assays Glutathione Transferase Glutathione Reductase Genetic Linkage Mutagenesis, Site-Directed Hexosaminidases Reference Values Recombinant Proteins Glucuronosyltransferase Models, Genetic Esterases Cholesterol

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