These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

199 related articles for article (PubMed ID: 23141293)

  • 1. DHTKD1 mutations cause 2-aminoadipic and 2-oxoadipic aciduria.
    Danhauser K; Sauer SW; Haack TB; Wieland T; Staufner C; Graf E; Zschocke J; Strom TM; Traub T; Okun JG; Meitinger T; Hoffmann GF; Prokisch H; Kölker S
    Am J Hum Genet; 2012 Dec; 91(6):1082-7. PubMed ID: 23141293
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic basis of alpha-aminoadipic and alpha-ketoadipic aciduria.
    Hagen J; te Brinke H; Wanders RJ; Knegt AC; Oussoren E; Hoogeboom AJ; Ruijter GJ; Becker D; Schwab KO; Franke I; Duran M; Waterham HR; Sass JO; Houten SM
    J Inherit Metab Dis; 2015 Sep; 38(5):873-9. PubMed ID: 25860818
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Elevated glutaric acid levels in Dhtkd1-/Gcdh- double knockout mice challenge our current understanding of lysine metabolism.
    Biagosch C; Ediga RD; Hensler SV; Faerberboeck M; Kuehn R; Wurst W; Meitinger T; Kölker S; Sauer S; Prokisch H
    Biochim Biophys Acta Mol Basis Dis; 2017 Sep; 1863(9):2220-2228. PubMed ID: 28545977
    [TBL] [Abstract][Full Text] [Related]  

  • 4. DHTKD1 Deficiency Causes Charcot-Marie-Tooth Disease in Mice.
    Xu WY; Zhu H; Shen Y; Wan YH; Tu XD; Wu WT; Tang L; Zhang HX; Lu SY; Jin XL; Fei J; Wang ZG
    Mol Cell Biol; 2018 Jul; 38(13):. PubMed ID: 29661920
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Structure-function analyses of the G729R 2-oxoadipate dehydrogenase genetic variant associated with a disorder of l-lysine metabolism.
    Zhang X; Nemeria NS; Leandro J; Houten S; Lazarus M; Gerfen G; Ozohanics O; Ambrus A; Nagy B; Brukh R; Jordan F
    J Biol Chem; 2020 Jun; 295(23):8078-8095. PubMed ID: 32303640
    [TBL] [Abstract][Full Text] [Related]  

  • 6. DHTKD1 and OGDH display substrate overlap in cultured cells and form a hybrid 2-oxo acid dehydrogenase complex in vivo.
    Leandro J; Dodatko T; Aten J; Nemeria NS; Zhang X; Jordan F; Hendrickson RC; Sanchez R; Yu C; DeVita RJ; Houten SM
    Hum Mol Genet; 2020 May; 29(7):1168-1179. PubMed ID: 32160276
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A nonsense mutation in DHTKD1 causes Charcot-Marie-Tooth disease type 2 in a large Chinese pedigree.
    Xu WY; Gu MM; Sun LH; Guo WT; Zhu HB; Ma JF; Yuan WT; Kuang Y; Ji BJ; Wu XL; Chen Y; Zhang HX; Sun FT; Huang W; Huang L; Chen SD; Wang ZG
    Am J Hum Genet; 2012 Dec; 91(6):1088-94. PubMed ID: 23141294
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Inhibition and Crystal Structure of the Human DHTKD1-Thiamin Diphosphate Complex.
    Leandro J; Khamrui S; Wang H; Suebsuwong C; Nemeria NS; Huynh K; Moustakim M; Secor C; Wang M; Dodatko T; Stauffer B; Wilson CG; Yu C; Arkin MR; Jordan F; Sanchez R; DeVita RJ; Lazarus MB; Houten SM
    ACS Chem Biol; 2020 Aug; 15(8):2041-2047. PubMed ID: 32633484
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The mitochondrial 2-oxoadipate and 2-oxoglutarate dehydrogenase complexes share their E2 and E3 components for their function and both generate reactive oxygen species.
    Nemeria NS; Gerfen G; Nareddy PR; Yang L; Zhang X; Szostak M; Jordan F
    Free Radic Biol Med; 2018 Feb; 115():136-145. PubMed ID: 29191460
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A patient with alpha-ketoadipic and alpha-aminoadipic aciduria.
    Duran M; Beemer FA; Wadman SK; Wendel U; Janssen B
    J Inherit Metab Dis; 1984; 7(2):61. PubMed ID: 6434826
    [No Abstract]   [Full Text] [Related]  

  • 11. Production of superoxide/hydrogen peroxide by the mitochondrial 2-oxoadipate dehydrogenase complex.
    Goncalves RL; Bunik VI; Brand MD
    Free Radic Biol Med; 2016 Feb; 91():247-55. PubMed ID: 26708453
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A fatal case of 2-keto-, 2-hydroxy- and 2-aminoadipic aciduria: relation of organic aciduria to phenotype?
    Jakobs C; de Grauw AJ
    J Inherit Metab Dis; 1992; 15(2):279-80. PubMed ID: 1527995
    [No Abstract]   [Full Text] [Related]  

  • 13. Heterozygous
    Osmanovic A; Gogol I; Martens H; Widjaja M; Müller K; Schreiber-Katz O; Feuerhake F; Langhans CD; Schmidt G; Andersen PM; Ludolph AC; Weishaupt JH; Brand F; Petri S; Weber RG
    Genes (Basel); 2021 Dec; 13(1):. PubMed ID: 35052424
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A Korean girl with alpha-aminoadipic and alpha-ketoadipic aciduria accompanied with elevation of 2-hydroxyglutarate and glutarate.
    Lee JS; Yoon HR; Coe CJ
    J Inherit Metab Dis; 2001 Aug; 24(4):509-10. PubMed ID: 11596655
    [No Abstract]   [Full Text] [Related]  

  • 15. alpha-Aminoadipic and alpha-ketoadipic aciduria: detection of a new case by a screening program using two-dimensional thin layer chromatography of amino acids.
    Vianey-Liaud C; Divry P; Cotte J; Teyssier G
    J Inherit Metab Dis; 1985; 8 Suppl 2():133-4. PubMed ID: 3930865
    [No Abstract]   [Full Text] [Related]  

  • 16. Human 2-Oxoglutarate Dehydrogenase and 2-Oxoadipate Dehydrogenase Both Generate Superoxide/H
    Jordan F; Nemeria N; Gerfen G
    Neurochem Res; 2019 Oct; 44(10):2325-2335. PubMed ID: 30847859
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Whole-exome sequencing uncovers oxidoreductases DHTKD1 and OGDHL as linkers between mitochondrial dysfunction and eosinophilic esophagitis.
    Sherrill JD; Kc K; Wang X; Wen T; Chamberlin A; Stucke EM; Collins MH; Abonia JP; Peng Y; Wu Q; Putnam PE; Dexheimer PJ; Aronow BJ; Kottyan LC; Kaufman KM; Harley JB; Huang T; Rothenberg ME
    JCI Insight; 2018 Apr; 3(8):. PubMed ID: 29669943
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Crystal structure and interaction studies of human DHTKD1 provide insight into a mitochondrial megacomplex in lysine catabolism.
    Bezerra GA; Foster WR; Bailey HJ; Hicks KG; Sauer SW; Dimitrov B; McCorvie TJ; Okun JG; Rutter J; Kölker S; Yue WW
    IUCrJ; 2020 Jul; 7(Pt 4):693-706. PubMed ID: 32695416
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Alpha-aminoadipic aciduria, a non-deleterious inborn metabolic defect.
    Fischer MH; Gerritsen T; Opitz JM
    Humangenetik; 1974; 24(4):265-70. PubMed ID: 4442872
    [No Abstract]   [Full Text] [Related]  

  • 20. Synthetic analogues of 2-oxo acids discriminate metabolic contribution of the 2-oxoglutarate and 2-oxoadipate dehydrogenases in mammalian cells and tissues.
    Artiukhov AV; Grabarska A; Gumbarewicz E; Aleshin VA; Kähne T; Obata T; Kazantsev AV; Lukashev NV; Stepulak A; Fernie AR; Bunik VI
    Sci Rep; 2020 Feb; 10(1):1886. PubMed ID: 32024885
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.