20-hydroxy-5,8,11,14-eicosatetraenoic acid has been researched along with Genetic Predisposition in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (42.86) | 29.6817 |
2010's | 4 (57.14) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bonafini, S; Fava, C | 1 |
Falck, JR; Fan, F; Garrett, MR; Juncos, LA; Muroya, Y; Regner, KR; Roman, RJ | 1 |
Liao, D; Lin, J; Yi, X; Zhang, B; Zhou, Q | 1 |
Lin, J; Wang, C; Yi, X; Zhou, Q | 1 |
Almgren, P; Berglund, G; Engström, G; Fava, C; Hedblad, B; Lippi, G; Melander, O; Minuz, P; Montagnana, M; Rosberg, L | 1 |
Dahly-Vernon, AJ; dos Santos, EA; Flasch, AK; Hoagland, KM; Knepper, MA; Roman, RJ | 1 |
Bellamine, A; Brown, NJ; Capdevila, JH; Cupples, LA; Dawson, EP; Demissie, S; Gainer, JV; Grant, SW; Guo, CY; O'Donnell, CJ; Wang, Y; Waterman, MR; Womble, KE | 1 |
1 review(s) available for 20-hydroxy-5,8,11,14-eicosatetraenoic acid and Genetic Predisposition
Article | Year |
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Eicosanoids via CYP450 and cardiovascular disease: Hints from genetic and nutrition studies.
Topics: Cardiovascular Diseases; Cytochrome P-450 Enzyme System; Eicosanoids; Genetic Predisposition to Disease; Genome-Wide Association Study; Haplotypes; Humans; Hydroxyeicosatetraenoic Acids; Nutrition Disorders; Polymorphism, Single Nucleotide | 2018 |
6 other study(ies) available for 20-hydroxy-5,8,11,14-eicosatetraenoic acid and Genetic Predisposition
Article | Year |
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Deficiency in the Formation of 20-Hydroxyeicosatetraenoic Acid Enhances Renal Ischemia-Reperfusion Injury.
Topics: Acute Kidney Injury; Animals; Cytochrome P-450 CYP4A; Gene Expression Regulation; Genetic Predisposition to Disease; Hydroxyeicosatetraenoic Acids; Kidney; Male; Rats; Rats, Sprague-Dawley; Reperfusion Injury | 2015 |
Interaction Between CYP4F2 rs2108622 and CPY4A11 rs9333025 Variants Is Significantly Correlated with Susceptibility to Ischemic Stroke and 20-Hydroxyeicosatetraenoic Acid Level.
Topics: Aged; Brain Ischemia; Case-Control Studies; Cytochrome P-450 CYP4A; Cytochrome P450 Family 4; Epistasis, Genetic; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Humans; Hydroxyeicosatetraenoic Acids; Male; Middle Aged; Polymorphism, Single Nucleotide; Stroke | 2016 |
CYP Genetic Variants, CYP Metabolite Levels, and Neurologic Deterioration in Acute Ischemic Stroke in Chinese Population.
Topics: Aged; Aged, 80 and over; Asian People; Biomarkers; Brain Ischemia; Chi-Square Distribution; China; Cytochrome P-450 CYP2C8; Cytochrome P-450 CYP4A; Cytochrome P-450 Enzyme System; Eicosanoids; Epoxide Hydrolases; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Humans; Hydroxyeicosatetraenoic Acids; Male; Middle Aged; Nerve Degeneration; Odds Ratio; Phenotype; Polymorphism, Single Nucleotide; Prospective Studies; Risk Factors; Stroke; Time Factors | 2017 |
The V433M variant of the CYP4F2 is associated with ischemic stroke in male Swedes beyond its effect on blood pressure.
Topics: Analysis of Variance; Anthropometry; Brain Ischemia; Cohort Studies; Cytochrome P-450 CYP4A; Female; Gene Expression Regulation; Genetic Predisposition to Disease; Genotype; Heterozygote; Humans; Hydroxyeicosatetraenoic Acids; Hypertension; Kaplan-Meier Estimate; Male; Middle Aged; Polymorphism, Genetic; Probability; Proportional Hazards Models; Sex Factors; Stroke | 2008 |
Elevated BSC-1 and ROMK expression in Dahl salt-sensitive rat kidneys.
Topics: Animals; Animals, Genetically Modified; Arachidonic Acid; Blood Pressure; Chromosomes; Cytochrome P-450 CYP4A; Diet, Sodium-Restricted; Genetic Predisposition to Disease; Hydroxyeicosatetraenoic Acids; Hypertension; Ion Transport; Kidney Cortex; Kidney Medulla; Loop of Henle; Male; Natriuresis; Potassium Channels; Potassium Channels, Inwardly Rectifying; Rats; Rats, Inbred BN; Rats, Inbred Dahl; Sodium; Sodium Chloride, Dietary; Sodium-Hydrogen Exchanger 3; Sodium-Hydrogen Exchangers; Sodium-Potassium-Chloride Symporters; Sodium-Potassium-Exchanging ATPase; Solute Carrier Family 12, Member 1 | 2004 |
Functional variant of CYP4A11 20-hydroxyeicosatetraenoic acid synthase is associated with essential hypertension.
Topics: Adult; Aged; Alleles; Amino Acid Substitution; Arachidonic Acid; Black People; Blood Pressure; Codon; Cohort Studies; Comorbidity; Cytochrome P-450 CYP4A; Cytochrome P-450 Enzyme System; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Humans; Hydroxyeicosatetraenoic Acids; Hypertension; Introns; Kidney; Lauric Acids; Male; Middle Aged; Multifactorial Inheritance; Mutagenesis, Insertional; Mutation, Missense; Point Mutation; Sequence Deletion; Tennessee; United States; White People | 2005 |