ornithine has been researched along with Genetic Predisposition in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 3 (60.00) | 24.3611 |
| 2020's | 1 (20.00) | 2.80 |
| Authors | Studies |
|---|---|
| Aglago, EK; Aleksandrova, K; Amiano, P; Bueno-de-Mesquita, B; Colorado-Yohar, SM; Dahm, CC; Fedirko, V; Freisling, H; Gram, IT; Gunter, MJ; Gurrea, AB; Heath, AK; Hughes, DJ; Jakszyn, P; Jenab, M; Jiao, L; Johnson, T; Katzke, V; Macciotta, A; Masala, G; Mayén, AL; Olsen, A; Perez-Cornago, A; Sánchez, MJ; Sandanger, T; Schalkwijk, CG; Schulze, MB; Sieri, S; Simeon, V; Skeie, G; Tjønneland, A; Tumino, R; Weiderpass, E | 1 |
| Ahmadi, A; Beisswenger, PJ; Blackburn, NJR; Brownlee, M; Cimenci, CE; Gonzalez-Gomez, M; McNeill, B; Milne, RW; Ostojic, A; Suuronen, EJ; Vulesevic, B; Zhong, Z | 1 |
| Atawia, RT; Bagi, Z; Bhatta, A; Caldwell, RB; Caldwell, RW; Chen, J; Fouda, AY; Lucas, R; Toque, HA; Xu, Z; Yao, L | 1 |
| Antonishyn, N; Irvine, J; Lehotay, DC; Lepage, J; McDonald, R; Rockman-Greenberg, C; Sokoro, AA | 1 |
| Abu-Amero, KK; Al-Dirbashi, OY; Al-Hassnan, ZN; Patay, Z; Rahbeeni, Z; Rashed, MS | 1 |
5 other study(ies) available for ornithine and Genetic Predisposition
| Article | Year |
|---|---|
Plasma concentrations of advanced glycation end-products and colorectal cancer risk in the EPIC study.
Topics: Adult; Aged; Chromatography, Liquid; Cohort Studies; Colorectal Neoplasms; Female; Genetic Association Studies; Genetic Predisposition to Disease; Glycation End Products, Advanced; Humans; Imidazoles; Lysine; Male; Middle Aged; Odds Ratio; Ornithine; Tandem Mass Spectrometry | 2021 |
Methylglyoxal-derived advanced glycation end products contribute to negative cardiac remodeling and dysfunction post-myocardial infarction.
Topics: Animals; Apoptosis; Cells, Cultured; Collagen Type I; Disease Models, Animal; Genetic Predisposition to Disease; Glycation End Products, Advanced; Human Umbilical Vein Endothelial Cells; Humans; Imidazoles; Lactoylglutathione Lyase; Mice, Inbred C57BL; Mice, Transgenic; Myocardial Infarction; Myocardium; Neovascularization, Physiologic; Ornithine; Phenotype; Pyruvaldehyde; Signal Transduction; Stem Cells; Time Factors; Ventricular Dysfunction, Left; Ventricular Function, Left; Ventricular Remodeling | 2017 |
Obesity-induced vascular dysfunction and arterial stiffening requires endothelial cell arginase 1.
Topics: Animals; Arginase; Arginine; Blood Glucose; Blood Pressure; Diabetes Mellitus, Experimental; Diabetes Mellitus, Type 2; Diet, High-Fat; Dietary Sucrose; Endothelium, Vascular; Enzyme Inhibitors; Fibrosis; Genetic Predisposition to Disease; Insulin; Male; Metabolic Syndrome; Mice, Inbred C57BL; Mice, Knockout; Nitric Oxide; Obesity; Ornithine; Oxidative Stress; Phenotype; Signal Transduction; Vascular Diseases; Vascular Stiffness; Vasodilation | 2017 |
Diagnosis and high incidence of hyperornithinemia-hyperammonemia-homocitrullinemia (HHH) syndrome in northern Saskatchewan.
Topics: Amino Acid Transport Systems, Basic; Biomarkers; DNA Mutational Analysis; Dried Blood Spot Testing; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Heterozygote; Homozygote; Humans; Hyperammonemia; Incidence; Infant, Newborn; Mitochondrial Membrane Transport Proteins; Mutation; Neonatal Screening; Ornithine; Phenotype; Polymerase Chain Reaction; Predictive Value of Tests; Prospective Studies; Retrospective Studies; Saskatchewan; Tandem Mass Spectrometry; Time Factors; Urea Cycle Disorders, Inborn | 2010 |
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome with stroke-like imaging presentation: clinical, biochemical and molecular analysis.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acid Transport Systems, Basic; Brain; Brain Diseases, Metabolic, Inborn; Child; Child, Preschool; Citrulline; DNA Mutational Analysis; Female; Food, Formulated; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Hyperammonemia; Magnetic Resonance Imaging; Male; Mitochondrial Membrane Transport Proteins; Mutation; Ornithine; Pedigree; Saudi Arabia; Sodium Benzoate; Stroke | 2008 |