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Journal Abstract Search

199 related items for PubMed ID: 19786097

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  • 2. Triosephosphate isomerase deficiency: facts and doubts.
    Orosz F, Oláh J, Ovádi J.
    IUBMB Life; 2006 Dec; 58(12):703-15. PubMed ID: 17424909
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  • 3. Triosephosphate isomerase I170V alters catalytic site, enhances stability and induces pathology in a Drosophila model of TPI deficiency.
    Roland BP, Amrich CG, Kammerer CJ, Stuchul KA, Larsen SB, Rode S, Aslam AA, Heroux A, Wetzel R, VanDemark AP, Palladino MJ.
    Biochim Biophys Acta; 2015 Jan; 1852(1):61-9. PubMed ID: 25463631
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  • 4. Evidence of a triosephosphate isomerase non-catalytic function crucial to behavior and longevity.
    Roland BP, Stuchul KA, Larsen SB, Amrich CG, Vandemark AP, Celotto AM, Palladino MJ.
    J Cell Sci; 2013 Jul 15; 126(Pt 14):3151-8. PubMed ID: 23641070
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  • 5. Triosephosphate isomerase deficiency: predictions and facts.
    Orosz F, Vértessy BG, Hollán S, Horányi M, Ovádi J.
    J Theor Biol; 1996 Oct 07; 182(3):437-47. PubMed ID: 8944178
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  • 6. Low catalytic activity is insufficient to induce disease pathology in triosephosphate isomerase deficiency.
    Segal J, Mülleder M, Krüger A, Adler T, Scholze-Wittler M, Becker L, Calzada-Wack J, Garrett L, Hölter SM, Rathkolb B, Rozman J, Racz I, Fischer R, Busch DH, Neff F, Klingenspor M, Klopstock T, Grüning NM, Michel S, Lukaszewska-McGreal B, Voigt I, Hartmann L, Timmermann B, Lehrach H, Wolf E, Wurst W, Gailus-Durner V, Fuchs H, H de Angelis M, Schrewe H, Yuneva M, Ralser M.
    J Inherit Metab Dis; 2019 Sep 07; 42(5):839-849. PubMed ID: 31111503
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  • 7. The feasibility of replacement therapy for inherited disorder of glycolysis: triosephosphate isomerase deficiency (review).
    Ationu A, Humphries A.
    Int J Mol Med; 1998 Dec 07; 2(6):701-4. PubMed ID: 9850739
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  • 9. Structural and Genetic Studies Demonstrate Neurologic Dysfunction in Triosephosphate Isomerase Deficiency Is Associated with Impaired Synaptic Vesicle Dynamics.
    Roland BP, Zeccola AM, Larsen SB, Amrich CG, Talsma AD, Stuchul KA, Heroux A, Levitan ES, VanDemark AP, Palladino MJ.
    PLoS Genet; 2016 Mar 07; 12(3):e1005941. PubMed ID: 27031109
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  • 10. Triose phosphate isomerase deficiency is caused by altered dimerization--not catalytic inactivity--of the mutant enzymes.
    Ralser M, Heeren G, Breitenbach M, Lehrach H, Krobitsch S.
    PLoS One; 2006 Dec 20; 1(1):e30. PubMed ID: 17183658
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  • 11. Missense variant in TPI1 (Arg189Gln) causes neurologic deficits through structural changes in the triosephosphate isomerase catalytic site and reduced enzyme levels in vivo.
    Roland BP, Richards KR, Hrizo SL, Eicher S, Barile ZJ, Chang TC, Savon G, Bianchi P, Fermo E, Ricerca BM, Tortorolo L, Vockley J, VanDemark AP, Palladino MJ.
    Biochim Biophys Acta Mol Basis Dis; 2019 Sep 01; 1865(9):2257-2266. PubMed ID: 31075491
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