aminoimidazole carboxamide has been researched along with Genetic Predisposition in 4 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 | 3 (75.00) | 24.3611 |
| 2020's | 1 (25.00) | 2.80 |
| Authors | Studies |
|---|---|
| Gui, Y; Hu, Z; Huang, C; Li, R; Ling, Z; Wang, Y; Yao, Y | 1 |
| Ma, A; Wang, J; Zhao, M; Zhu, H | 1 |
| Chen, BC; Duley, JA; Khoo, TB; McGown, IN; Ngu, LH; Pitt, J; Thong, MK; Yunus, ZM | 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 |
4 other study(ies) available for aminoimidazole carboxamide and Genetic Predisposition
| Article | Year |
|---|---|
5-Amino-4-Imidazolecarboxamide Ribonucleotide Transformylase/IMP Cyclohydrolase Polymorphisms Affect the Susceptibility to Multiple Myeloma.
Topics: Aminoimidazole Carboxamide; Gene Frequency; Genetic Predisposition to Disease; Genotype; Haplotypes; Humans; Hydroxymethyl and Formyl Transferases; Multienzyme Complexes; Multiple Myeloma; Nucleotide Deaminases; Polymorphism, Single Nucleotide; Ribonucleotides | 2022 |
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 |
Adenylosuccinate lyase deficiency in a Malaysian patient, with novel adenylosuccinate lyase gene mutations.
Topics: Adenosine; Adenosine Monophosphate; Adenylosuccinate Lyase; Aminoimidazole Carboxamide; Autistic Disorder; Biomarkers; Child Development; Chromatography, High Pressure Liquid; DNA Mutational Analysis; Genetic Predisposition to Disease; Genetic Testing; Heterozygote; Humans; Infant; Infant, Newborn; Malaysia; Male; Mutation; Myoclonus; Phenotype; Predictive Value of Tests; Psychomotor Disorders; Psychomotor Performance; Purine-Pyrimidine Metabolism, Inborn Errors; Ribonucleosides; Seizures; Spectrometry, Mass, Electrospray Ionization; Tandem Mass Spectrometry | 2010 |
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 |