aica ribonucleotide has been researched along with Genetic Predisposition in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ma, A; Wang, J; Zhao, M; Zhu, H | 1 |
| Baldoin, MC; Basso, G; Burlina, A; Desbats, MA; Doimo, M; Graziano, C; Lenzini, E; Murphy, E; Salviati, L; Sartori, G; Seri, M; Trevisson, E | 1 |
2 other study(ies) available for aica ribonucleotide and Genetic Predisposition
| Article | Year |
|---|---|
AMPK activation reduces the number of atheromata macrophages in ApoE deficient mice.
Topics: Aminoimidazole Carboxamide; AMP-Activated Protein Kinases; Animals; Antigens, Ly; Aorta; Aortic Diseases; Apolipoproteins E; Atherosclerosis; Biphenyl Compounds; Cell Line; Cell Migration Inhibition; Chemotaxis; Disease Models, Animal; Enzyme Activation; Enzyme Activators; Genetic Predisposition to Disease; Humans; Macrophages; Metformin; Mice, Knockout; Phenotype; Pyrones; Receptors, CCR2; Ribonucleotides; Signal Transduction; Thiophenes | 2017 |
Functional analysis of missense mutations of OAT, causing gyrate atrophy of choroid and retina.
Topics: Amino Acid Sequence; Aminoimidazole Carboxamide; Cells, Cultured; DNA Mutational Analysis; Fibroblasts; Genetic Complementation Test; Genetic Predisposition to Disease; Genotype; Gyrate Atrophy; HEK293 Cells; Humans; Immunoblotting; Models, Molecular; Molecular Sequence Data; Mutation, Missense; Ornithine-Oxo-Acid Transaminase; Phenotype; Protein Structure, Tertiary; Ribonucleotides; Saccharomyces cerevisiae; Sequence Homology, Amino Acid | 2013 |