citric acid, anhydrous has been researched along with Brain Diseases, Metabolic, Familial in 3 studies
Citric Acid: A key intermediate in metabolism. It is an acid compound found in citrus fruits. The salts of citric acid (citrates) can be used as anticoagulants due to their calcium chelating ability.
citric acid : A tricarboxylic acid that is propane-1,2,3-tricarboxylic acid bearing a hydroxy substituent at position 2. It is an important metabolite in the pathway of all aerobic organisms.
| 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 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Majd, H | 1 |
| King, MS | 1 |
| Smith, AC | 1 |
| Kunji, ERS | 1 |
| Pop, A | 2 |
| Williams, M | 1 |
| Struys, EA | 2 |
| Monné, M | 1 |
| Jansen, EEW | 1 |
| De Grassi, A | 1 |
| Kanhai, WA | 2 |
| Scarcia, P | 1 |
| Ojeda, MRF | 1 |
| Porcelli, V | 1 |
| van Dooren, SJM | 1 |
| Lennertz, P | 1 |
| Nota, B | 2 |
| Abdenur, JE | 1 |
| Coman, D | 1 |
| Das, AM | 1 |
| El-Gharbawy, A | 1 |
| Nuoffer, JM | 2 |
| Polic, B | 1 |
| Santer, R | 2 |
| Weinhold, N | 1 |
| Zuccarelli, B | 1 |
| Palmieri, F | 1 |
| Palmieri, L | 1 |
| Salomons, GS | 2 |
| Jansen, EE | 1 |
| Fernandez Ojeda, MR | 1 |
| Kranendijk, M | 1 |
| van Dooren, SJ | 1 |
| Bevova, MR | 1 |
| Sistermans, EA | 1 |
| Nieuwint, AW | 1 |
| Barth, M | 1 |
| Ben-Omran, T | 1 |
| Hoffmann, GF | 1 |
| de Lonlay, P | 1 |
| McDonald, MT | 1 |
| Meberg, A | 1 |
| Muntau, AC | 1 |
| Parini, R | 1 |
| Read, MH | 1 |
| Renneberg, A | 1 |
| Strahleck, T | 1 |
| van Schaftingen, E | 1 |
| van der Knaap, MS | 1 |
| Jakobs, C | 1 |
3 other studies available for citric acid, anhydrous and Brain Diseases, Metabolic, Familial
| Article | Year |
|---|---|
Pathogenic mutations of the human mitochondrial citrate carrier SLC25A1 lead to impaired citrate export required for lipid, dolichol, ubiquinone and sterol synthesis.
Topics: Anion Transport Proteins; Biological Transport, Active; Brain Diseases, Metabolic, Inborn; Catalytic | 2018 |
An overview of combined D-2- and L-2-hydroxyglutaric aciduria: functional analysis of CIC variants.
Topics: Anion Transport Proteins; Biological Assay; Brain Diseases, Metabolic, Inborn; Cells, Cultured; Chil | 2018 |
Deficiency in SLC25A1, encoding the mitochondrial citrate carrier, causes combined D-2- and L-2-hydroxyglutaric aciduria.
Topics: Amino Acid Sequence; Anion Transport Proteins; Biomarkers; Brain Diseases, Metabolic, Inborn; Case-C | 2013 |