Compounds > beta-resorcylic acid

beta-resorcylic acid and ubiquinone

beta-resorcylic acid has been researched along with ubiquinone in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's4 (66.67)24.3611
2020's2 (33.33)2.80

Authors

AuthorsStudies
Acuña-Castroviejo, D; Barca, E; Cobos, EJ; Díaz-Casado, E; Escames, G; López, LC; Luna-Sánchez, M; Montilla-García, Á; Quinzii, CM; Tejada, MÁ1
Andeer, R; Barbaro, M; Bruhn, H; Engvall, M; Felser, A; Freyer, C; Hinze, Y; Lesko, N; Maffezzini, C; Magnusson, M; Mourier, A; Naess, K; Stranneheim, H; von Döbeln, U; Wedell, A; Wibom, R; Wredenberg, A; Zetterström, RH1
Hekimi, S; Innes, M; Khan, A; Parboosingh, JS; Smith, C; Wang, Y1
Acuña-Castroviejo, D; Bakkali, M; Barriocanal-Casado, E; Díaz-Casado, ME; Duarte, J; Escames, G; Hidalgo-Gutiérrez, A; López, LC; Prehn, C; Romero, M; Sánchez-Maldonado, L; Sayed, RK1
Buerger, F; Choi, WI; Chung, YW; Clarke, CF; Fernández-Del-Río, L; Gee, HY; Helmstädter, M; Hildebrandt, F; Hugo, H; Kim, JW; Lee, MG; Nag, A; Nakayama, M; Ryu, JH; Schapiro, D; Widmeier, E; Yu, S1
Daehn, IS1

Other Studies

6 other study(ies) available for beta-resorcylic acid and ubiquinone

ArticleYear
The clinical heterogeneity of coenzyme Q10 deficiency results from genotypic differences in the Coq9 gene.
    EMBO molecular medicine, 2015, Volume: 7, Issue:5

    Topics: Animals; Ataxia; Disease Models, Animal; Genetic Variation; Genotype; Hydroxybenzoates; Mammals; Mice; Mice, Transgenic; Mitochondrial Diseases; Muscle Weakness; Mutation, Missense; Ubiquinone

2015
Rescue of primary ubiquinone deficiency due to a novel COQ7 defect using 2,4-dihydroxybensoic acid.
    Journal of medical genetics, 2015, Volume: 52, Issue:11

    Topics: Amino Acid Sequence; Ataxia; Child; Child, Preschool; Chromatography, Liquid; DNA Mutational Analysis; Exome; Homozygote; Humans; Hydroxybenzoates; Infant, Newborn; Male; Mitochondria; Mitochondrial Diseases; Molecular Sequence Data; Muscle Weakness; Mutation, Missense; Sequence Alignment; Tandem Mass Spectrometry; Ubiquinone

2015
Pathogenicity of two COQ7 mutations and responses to 2,4-dihydroxybenzoate bypass treatment.
    Journal of cellular and molecular medicine, 2017, Volume: 21, Issue:10

    Topics: Animals; Base Sequence; Cell Line; Child; Consanguinity; Cytochrome P-450 Enzyme System; DNA Mutational Analysis; DNA, Mitochondrial; Female; Fibroblasts; Hearing Loss; Humans; Hydroxybenzoates; Membrane Proteins; Mice, Knockout; Mitochondrial Proteins; Mixed Function Oxygenases; Mutation; Spastic Paraplegia, Hereditary; Ubiquinone

2017
β-RA reduces DMQ/CoQ ratio and rescues the encephalopathic phenotype in
    EMBO molecular medicine, 2019, Volume: 11, Issue:1

    Topics: Animals; Brain; Disease Models, Animal; Energy Metabolism; Histocytochemistry; Hydroxybenzoates; Mice; Mitochondrial Encephalomyopathies; Neuroprotective Agents; Salicylic Acid; Survival Analysis; Treatment Outcome; Ubiquinone

2019
ADCK4 Deficiency Destabilizes the Coenzyme Q Complex, Which Is Rescued by 2,4-Dihydroxybenzoic Acid Treatment.
    Journal of the American Society of Nephrology : JASN, 2020, Volume: 31, Issue:6

    Topics: Animals; Enzyme Stability; Glomerulosclerosis, Focal Segmental; HEK293 Cells; Humans; Hydroxybenzoates; Methyltransferases; Mice; Mice, Inbred C57BL; Mitochondria; Mitochondrial Proteins; Podocytes; Protein Kinases; Ubiquinone

2020
Mitochondria Matter: A Critical Role of
    Journal of the American Society of Nephrology : JASN, 2020, Volume: 31, Issue:6

    Topics: Humans; Hydroxybenzoates; Mitochondria; Nephrotic Syndrome; Podocytes; Steroids; Ubiquinone

2020