citric acid, anhydrous and alpha-hydroxyglutarate

citric acid, anhydrous has been researched along with alpha-hydroxyglutarate in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (25.00)29.6817
2010's2 (50.00)24.3611
2020's1 (25.00)2.80

Authors

AuthorsStudies
Gibson, KM; Jakobs, C; Struys, EA1
Barth, M; Ben-Omran, T; Bevova, MR; de Lonlay, P; Fernandez Ojeda, MR; Hoffmann, GF; Jakobs, C; Jansen, EE; Kanhai, WA; Kranendijk, M; McDonald, MT; Meberg, A; Muntau, AC; Nieuwint, AW; Nota, B; Nuoffer, JM; Parini, R; Pop, A; Read, MH; Renneberg, A; Salomons, GS; Santer, R; Sistermans, EA; Strahleck, T; Struys, EA; van der Knaap, MS; van Dooren, SJ; van Schaftingen, E1
Abdenur, JE; Coman, D; Das, AM; De Grassi, A; El-Gharbawy, A; Jansen, EEW; Kanhai, WA; Lennertz, P; Monné, M; Nota, B; Nuoffer, JM; Ojeda, MRF; Palmieri, F; Palmieri, L; Polic, B; Pop, A; Porcelli, V; Salomons, GS; Santer, R; Scarcia, P; Struys, EA; van Dooren, SJM; Weinhold, N; Williams, M; Zuccarelli, B1
Arós, F; Bulló, M; Clish, C; Corella, D; Estruch, R; Fitó, M; García-Gavilán, J; Guasch-Ferré, M; Hu, FB; Lee, CH; Li, J; Liang, L; Martínez-González, MA; Papandreou, C; Pierce, K; Razquin, C; Ros, E; Ruiz-Canela, M; Salas-Salvadó, J; Serra-Majem, L; Toledo, E1

Other Studies

4 other study(ies) available for citric acid, anhydrous and alpha-hydroxyglutarate

ArticleYear
Novel insights into L-2-hydroxyglutaric aciduria: mass isotopomer studies reveal 2-oxoglutaric acid as the metabolic precursor of L-2-hydroxyglutaric acid.
    Journal of inherited metabolic disease, 2007, Volume: 30, Issue:5

    Topics: Alcohol Oxidoreductases; Carbon Isotopes; Cell Line; Citric Acid; Deuterium; Gas Chromatography-Mass Spectrometry; Glucose; Glutamic Acid; Glutarates; Humans; Ketoglutaric Acids; Lymphocytes; Metabolism, Inborn Errors; Oxidation-Reduction

2007
Deficiency in SLC25A1, encoding the mitochondrial citrate carrier, causes combined D-2- and L-2-hydroxyglutaric aciduria.
    American journal of human genetics, 2013, Apr-04, Volume: 92, Issue:4

    Topics: Amino Acid Sequence; Anion Transport Proteins; Biomarkers; Brain Diseases, Metabolic, Inborn; Case-Control Studies; Cells, Cultured; Chromatography, Liquid; Citric Acid; Exome; Female; Fibroblasts; Genes, Recessive; Glutarates; Humans; Male; Mitochondria; Mitochondrial Proteins; Molecular Sequence Data; Mutation; Organic Anion Transporters; Phenotype; Protein Structure, Tertiary; Retrospective Studies; Sequence Homology, Amino Acid; Stereoisomerism; Tandem Mass Spectrometry

2013
An overview of combined D-2- and L-2-hydroxyglutaric aciduria: functional analysis of CIC variants.
    Journal of inherited metabolic disease, 2018, Volume: 41, Issue:2

    Topics: Anion Transport Proteins; Biological Assay; Brain Diseases, Metabolic, Inborn; Cells, Cultured; Child, Preschool; Citric Acid; DNA Mutational Analysis; Female; Fibroblasts; Genetic Predisposition to Disease; Glutarates; Humans; Infant; Infant, Newborn; Male; Mitochondrial Proteins; Models, Molecular; Mutation, Missense; Organic Anion Transporters; Phenotype; Protein Conformation; Structure-Activity Relationship

2018
Tricarboxylic acid cycle related-metabolites and risk of atrial fibrillation and heart failure.
    Metabolism: clinical and experimental, 2021, Volume: 125

    Topics: Aconitic Acid; Aged; Atrial Fibrillation; Case-Control Studies; Citric Acid; Citric Acid Cycle; Female; Glutarates; Heart Failure; Humans; Incidence; Isocitrates; Malates; Male; Middle Aged; Risk; Succinic Acid

2021