leucine has been researched along with Carotid Artery Narrowing in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Karvonen, MK; Koulu, M; Laakso, M; Mercuri, M; Niskanen, L; Pesonen, U; Rauramaa, R; Töyry, J; Uusitupa, MI; Valve, R | 1 |
Brophy, VH; Furlong, CE; Hatsukami, TS; Jarvik, GP; Richter, RJ; Rozek, LS; Schellenberg, GD | 1 |
Gong, JS; Kawamori, R; Matsunaga, H; Nomiyama, T; Ogawa, O; Ogihara, T; Tanaka, M; Tanaka, Y; Yagi, K; Yamada, Y; Zhang, J | 1 |
3 other study(ies) available for leucine and Carotid Artery Narrowing
Article | Year |
---|---|
Leucine 7 to proline 7 polymorphism in the neuropeptide Y gene is associated with enhanced carotid atherosclerosis in elderly patients with type 2 diabetes and control subjects.
Topics: Aged; Amino Acid Substitution; Arteriosclerosis; Autonomic Nervous System; Blood Pressure; Carotid Stenosis; Cohort Studies; Cross-Sectional Studies; Diabetes Mellitus, Type 2; Diabetic Angiopathies; Female; Genotype; Heart Rate; Humans; Leucine; Male; Neuropeptide Y; Polymorphism, Genetic; Proline; Risk Factors | 2000 |
Paraoxonase (PON1) phenotype is a better predictor of vascular disease than is PON1(192) or PON1(55) genotype.
Topics: Aged; Aged, 80 and over; Amino Acid Substitution; Arginine; Aryldialkylphosphatase; Carotid Stenosis; Case-Control Studies; Esterases; Genotype; Glutamine; Haplotypes; Humans; Isoenzymes; Leucine; Male; Methionine; Middle Aged; Organophosphorus Compounds; Paraoxon; Phenotype; Predictive Value of Tests; Risk Factors | 2000 |
Antiatherogenic mitochondrial genotype in patients with type 2 diabetes.
Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Arteriosclerosis; Carotid Stenosis; Diabetes Mellitus, Type 2; DNA, Mitochondrial; Female; Genomic Imprinting; Genotype; Humans; Japan; Leucine; Longevity; Male; Methionine; Middle Aged; Mutation, Missense; NADH Dehydrogenase; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Reference Values; Regression Analysis | 2001 |