Available homocysteine. Medical search. Frequent questions

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Endothelium, Vascular Liver Cells, Cultured Erythrocytes Brachial Artery Carotid Arteries Muscle, Smooth, Vascular Kidney Tunica Intima Aorta

Organisms4

Cereals Rats, Sprague-Dawley Saccharomycopsis Vegetables

Diseases36

Hyperhomocysteinemia Homocystinuria Vitamin B 12 Deficiency Folic Acid Deficiency Vitamin B Deficiency Vitamin B 6 Deficiency Cardiovascular Diseases Vascular Diseases Neural Tube Defects Arteriosclerosis Choline Deficiency Kidney Failure, Chronic Coronary Disease Thrombophilia Coronary Artery Disease Thrombosis Stroke Atherosclerosis Peripheral Vascular Diseases Avitaminosis Amino Acid Metabolism, Inborn Errors Anemia, Pernicious Spinal Dysraphism Cerebrovascular Disorders Brain Ischemia Retinal Vein Occlusion Dementia Genetic Predisposition to Disease Leukoplakia Riboflavin Deficiency Myocardial Infarction Body Weight Intracranial Thrombosis Behcet Syndrome Diabetes Mellitus, Type 2 Disease Models, Animal

Chemicals and Drugs125

Vitamin B 12 Folic Acid Homocystine Cystathionine beta-Synthase Methylenetetrahydrofolate Reductase (NADPH2)Methionine Vitamin B Complex Vitamin B 6 Betaine-Homocysteine S-Methyltransferase Cystathionine 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase S-Adenosylhomocysteine Oxidoreductases Acting on CH-NH Group Donors Methylmalonic Acid Betaine S-Adenosylmethionine Homocysteine S-Methyltransferase Pyridoxine 5,10-Methylenetetrahydrofolate Reductase (FADH2)Glycine N-Methyltransferase Tetrahydrofolates Cysteine Adenosylhomocysteinase Transcobalamins Sarcosine Cystathionine gamma-Lyase Biological Markers Pyridoxal Phosphate Lipotropic Agents Cysteic Acid Methylenetetrahydrofolate Dehydrogenase (NAD+)Methyltransferases Phosphatidylethanolamine N-Methyltransferase Sulfhydryl Compounds Choline Ferredoxin-NADP Reductase Riboflavin Amino Acids, Sulfur Vitamins Sulfur Tubercidin Creatinine Hematinics Dipeptides Methionine-tRNA Ligase Copper Sulfate Guanidinoacetate N-Methyltransferase Methylenetetrahydrofolate Dehydrogenase (NADP)Glutathione Nicotinamide N-Methyltransferase Lipoprotein(a)Coffee C-Reactive Protein Methionine Adenosyltransferase Lipids Hydroxocobalamin Choline Dehydrogenase Vitamin U Lyases Hydrogen Sulfide Cystamine Cholesterol Reduced Folate Carrier Protein Cysteine Synthase Copper Nitrous Oxide Sulfur Compounds Sarcosine Dehydrogenase Amino Acids Mercaptoethanol Sulfinic Acids Cholesterol, HDL Hydrolases gamma-Glutamyl Hydrolase Antioxidants Serine Homoserine Placebos Fibrinogen Carbon-Oxygen Lyases Ethionine Aryldialkylphosphatase Glycine Hydroxymethyltransferase Malondialdehyde Sulfur Radioisotopes Triglycerides Cystine Ceruloplasmin Taurine Adenosine RNA, Messenger Carbon-Sulfur Lyases Glycine Sulfur Isotopes Arginine Formate-Tetrahydrofolate Ligase Micronutrients Annexin A2 Nitric Oxide Protein C Superoxide Dismutase Dietary Proteins Methotrexate Amino Acid Transport System y+L Creatine Amidinotransferases Soybean Proteins Xanthurenates Anethole Trithione Fibric Acids Blood Proteins Pyridoxal Blood Glucose Glutathione Peroxidase Methylmalonyl-CoA Mutase Reactive Oxygen Species Caseins Cholesterol, LDL Factor V Carbamazepine Acetylcysteine Serum Albumin Bepridil Penicillamine Catalase

Analytical, Diagnostic and Therapeutic Techniques and Equipment32

Risk Factors Case-Control Studies Fluorescence Polarization Immunoassay Reference Values Double-Blind Method Chromatography, High Pressure Liquid Cross-Sectional Studies Prospective Studies Regression Analysis Analysis of Variance Renal Dialysis Cohort Studies Linear Models Odds Ratio Cross-Over Studies Follow-Up Studies Nutrition Surveys Administration, Oral Diet, Vegetarian Placebos Multivariate Analysis Predictive Value of Tests Body Mass Index Blood Pressure Mendelian Randomization Analysis Statistics, Nonparametric Gas Chromatography-Mass Spectrometry Risk Assessment Body Weight Blood Chemical Analysis Incidence Disease Models, Animal

Psychiatry and Psychology6

Fasting Cognition Disorders Smoking Dementia Cognition Life Style

Phenomena and Processes32

Methylation Genotype Polymorphism, Genetic Diet Fasting Nutritional Status Dose-Response Relationship, Drug Homozygote Oxidative Stress Time Factors Aging Odds Ratio Oxidation-Reduction Mutation Diet, Vegetarian Kinetics Polymorphism, Single Nucleotide Pregnancy Hemostasis Body Mass Index Gene Frequency Vasodilation DNA Methylation Point Mutation Blood Pressure Sex Characteristics Osmolar Concentration Genetic Predisposition to Disease Lipid Peroxidation Body Weight Up-Regulation Nutritional Requirements

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Risk Factors Case-Control Studies Nutritional Status Double-Blind Method Cross-Sectional Studies Prospective Studies Regression Analysis Analysis of Variance Cohort Studies Linear Models Odds Ratio Cross-Over Studies Sex Factors Follow-Up Studies Nutrition Surveys Age Factors Multivariate Analysis Predictive Value of Tests Body Mass Index Statistics, Nonparametric Risk Assessment Incidence

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

Hyperhomocysteinemia Vitamin B 12 Folic Acid Homocystine Cystathionine beta-Synthase Methylenetetrahydrofolate Reductase (NADPH2)Methionine Vitamin B Complex Vitamin B 6 Betaine-Homocysteine S-Methyltransferase Cystathionine 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase S-Adenosylhomocysteine Homocystinuria Oxidoreductases Acting on CH-NH Group Donors Vitamin B 12 Deficiency Folic Acid Deficiency Methylmalonic Acid Betaine S-Adenosylmethionine Homocysteine S-Methyltransferase Pyridoxine 5,10-Methylenetetrahydrofolate Reductase (FADH2)Glycine N-Methyltransferase Tetrahydrofolates Cysteine Dietary Supplements Risk Factors Adenosylhomocysteinase Vitamin B Deficiency Transcobalamins Vitamin B 6 Deficiency Sarcosine Methylation Cystathionine gamma-Lyase Biological Markers Genotype Pyridoxal Phosphate Lipotropic Agents Cardiovascular Diseases Polymorphism, Genetic Vascular Diseases Cysteic Acid Case-Control Studies Diet Methylenetetrahydrofolate Dehydrogenase (NAD+)Fasting Methyltransferases Phosphatidylethanolamine N-Methyltransferase Fluorescence Polarization Immunoassay Sulfhydryl Compounds Endothelium, Vascular Choline Ferredoxin-NADP Reductase Neural Tube Defects Reference Values Riboflavin Amino Acids, Sulfur Vitamins Nutritional Status Sulfur Food, Fortified Tubercidin Creatinine Arteriosclerosis Hematinics Dipeptides Methionine-tRNA Ligase Dose-Response Relationship, Drug Copper Sulfate Double-Blind Method Guanidinoacetate N-Methyltransferase Methylenetetrahydrofolate Dehydrogenase (NADP)Chromatography, High Pressure Liquid Glutathione Homozygote Cross-Sectional Studies Nicotinamide N-Methyltransferase Lipoprotein(a)Coffee Prospective Studies Choline Deficiency Liver C-Reactive Protein Oxidative Stress Regression Analysis Methionine Adenosyltransferase Analysis of Variance Kidney Failure, Chronic Coronary Disease Time Factors Lipids Hydroxocobalamin Choline Dehydrogenase Vitamin U Lyases Thrombophilia Cells, Cultured Coronary Artery Disease Erythrocytes

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