Liver activity homozygote. Medical search. Frequent questions

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Anatomy10

Liver Microsomes, Liver Mitochondria, Liver Hepatocytes Kupffer Cells Kidney Portal Vein Hepatic Artery Bile Ducts Cells, Cultured

Organisms7

Mice, Mutant Strains Rats, Inbred Strains Mice, Knockout Rats, Wistar Mice, Transgenic Rats, Sprague-Dawley Rats, Inbred F344

Diseases22

Liver Diseases Liver Neoplasms Liver Cirrhosis Fatty Liver Drug-Induced Liver Injury Liver Neoplasms, Experimental Hemochromatosis Genetic Predisposition to Disease Liver Failure, Acute Liver Abscess Liver Diseases, Alcoholic Liver Cirrhosis, Experimental Liver Cirrhosis, Alcoholic Carcinoma, Hepatocellular End Stage Liver Disease Albinism Hyperlipoproteinemia Type II Hepatitis Disease Models, Animal alpha 1-Antitrypsin Deficiency Gaucher Disease Hyperlipoproteinemia Type III

Chemicals and Drugs26

Liver Extracts Liver Glycogen Alanine Transaminase RNA, Messenger Apolipoprotein E2 DNA Catechol O-Methyltransferase Cytochrome P-450 Enzyme System Methylenetetrahydrofolate Reductase (NADPH2)Carbon Tetrachloride Membrane Proteins Cholesterol Triglycerides Ferritins Aryl Hydrocarbon Hydroxylases DNA Primers Iron Isoenzymes Lipids Genetic Markers Apolipoproteins E Carrier Proteins Histocompatibility Antigens Class I Bilirubin Glucuronosyltransferase Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment25

Liver Transplantation Liver Function Tests Liver Neoplasms, Experimental Hepatectomy Liver Cirrhosis, Experimental Case-Control Studies Liver, Artificial Heterozygote Detection Polymerase Chain Reaction Risk Factors Pedigree Crosses, Genetic Disease Models, Animal Organ Size Genetic Association Studies Genetic Testing DNA Mutational Analysis Chromosome Mapping Treatment Outcome Reference Values Amino Acid Substitution Cohort Studies Perfusion Reverse Transcriptase Polymerase Chain Reaction Models, Genetic

Phenomena and Processes35

Tissue Distribution Homozygote Heterozygote Liver Regeneration Genotype Polymorphism, Genetic Alleles Gene Frequency Liver Circulation Genetic Predisposition to Disease Polymorphism, Single Nucleotide Mutation Phenotype Base Sequence Haplotypes Genetic Variation Genes, Lethal Time Factors Genes, Recessive Kinetics Polymorphism, Restriction Fragment Length Point Mutation Organ Size Amino Acid Sequence Gene Expression Regulation Promoter Regions, Genetic Exons Gene Expression Linkage Disequilibrium Genetic Markers Lipid Metabolism Mutation, Missense Amino Acid Substitution Genes, Dominant Genetic Linkage

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Named Groups3

Asian Continental Ancestry Group European Continental Ancestry Group Living Donors

Health Care5

Case-Control Studies Risk Factors Genetic Testing Treatment Outcome Cohort Studies

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

Liver Tissue Distribution Homozygote Liver Diseases Liver Transplantation Liver Neoplasms Liver Cirrhosis Microsomes, Liver Heterozygote Liver Regeneration Fatty Liver Genotype Polymorphism, Genetic Liver Function Tests Mitochondria, Liver Alleles Drug-Induced Liver Injury Gene Frequency Liver Extracts Liver Circulation Liver Neoplasms, Experimental Hemochromatosis Genetic Predisposition to Disease Polymorphism, Single Nucleotide Liver Failure, Acute Mutation Liver Abscess Phenotype Liver Diseases, Alcoholic Hepatectomy Hepatocytes Liver Cirrhosis, Experimental Liver Cirrhosis, Alcoholic Case-Control Studies Base Sequence Haplotypes Liver, Artificial Liver Glycogen Genetic Variation Carcinoma, Hepatocellular Heterozygote Detection Molecular Sequence Data Mice, Mutant Strains Alanine Transaminase End Stage Liver Disease RNA, Messenger Polymerase Chain Reaction Genes, Lethal Rats, Inbred Strains Time Factors Risk Factors Apolipoprotein E2 DNA Genes, Recessive Catechol O-Methyltransferase Albinism Cytochrome P-450 Enzyme System Pedigree Hyperlipoproteinemia Type II Kinetics Crosses, Genetic Methylenetetrahydrofolate Reductase (NADPH2)Polymorphism, Restriction Fragment Length Hepatitis Mice, Knockout Carbon Tetrachloride Point Mutation Disease Models, Animal Kupffer Cells Membrane Proteins Asian Continental Ancestry Group Cholesterol Organ Size Amino Acid Sequence Genetic Association Studies Rats, Wistar Triglycerides Ferritins Aryl Hydrocarbon Hydroxylases Gene Expression Regulation DNA Primers Kidney Promoter Regions, Genetic Portal Vein Exons Gene Expression Genetic Testing Iron Mice, Transgenic Isoenzymes Lipids alpha 1-Antitrypsin Deficiency Linkage Disequilibrium Rats, Sprague-Dawley European Continental Ancestry Group DNA Mutational Analysis Hepatic Artery Chromosome Mapping Bile Ducts Genetic Markers

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