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Journal Abstract Search

148 related items for PubMed ID: 10910933

  • 21.
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  • 22. Prenatal diagnosis of triosephosphate isomerase deficiency.
    Arya R, Lalloz MR, Nicolaides KH, Bellingham AJ, Layton DM.
    Blood; 1996 Jun 01; 87(11):4507-9. PubMed ID: 8639817
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  • 27. [A case of congenital non-spherocytic hemolytic anemia caused by triose phosphate isomerase deficiency. Prenatal diagnosis].
    Poinsot J, Parent P, Alix D, Toudic L, Castel Y.
    J Genet Hum; 1986 Nov 01; 34(5):431-7. PubMed ID: 3794669
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  • 28. Triosephosphate isomerase deficiency: facts and doubts.
    Orosz F, Oláh J, Ovádi J.
    IUBMB Life; 2006 Dec 01; 58(12):703-15. PubMed ID: 17424909
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  • 29. 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 01; 42(5):839-849. PubMed ID: 31111503
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  • 32. Triosephosphate isomerase deficiency: haemolytic anaemia, myopathy with altered mitochondria and mental retardation due to a new variant with accelerated enzyme catabolism and diminished specific activity.
    Eber SW, Pekrun A, Bardosi A, Gahr M, Krietsch WK, Krüger J, Matthei R, Schröter W.
    Eur J Pediatr; 1991 Sep 01; 150(11):761-6. PubMed ID: 1959537
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  • 33. Bone marrow transplantation corrects haemolytic anaemia in a novel ENU mutagenesis mouse model of TPI deficiency.
    Conway AJ, Brown FC, Hortle EJ, Burgio G, Foote SJ, Morton CJ, Jane SM, Curtis DJ.
    Dis Model Mech; 2018 May 21; 11(5):. PubMed ID: 29720471
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  • 34. Triosephosphate isomerase deficiency with hemolytic anemia and severe neuromuscular disease: familial and biochemical studies of a case found in Spain.
    Vives-Corrons JL, Rubinson-Skala H, Mateo M, Estella J, Feliu E, Dreyfus JC.
    Hum Genet; 1978 Jun 09; 42(2):171-80. PubMed ID: 669702
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  • 35. Degradation of functional triose phosphate isomerase protein underlies sugarkill pathology.
    Seigle JL, Celotto AM, Palladino MJ.
    Genetics; 2008 Jun 09; 179(2):855-62. PubMed ID: 18458110
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  • 36. Identification of protein quality control regulators using a Drosophila model of TPI deficiency.
    Hrizo SL, Eicher SL, Myers TD, McGrath I, Wodrich APK, Venkatesh H, Manjooran D, Swoger S, Gagnon K, Bruskin M, Lebedev MV, Zheng S, Vitantonio A, Kim S, Lamb ZJ, Vogt A, Ruzhnikov MRZ, Palladino MJ.
    Neurobiol Dis; 2021 May 09; 152():105299. PubMed ID: 33600953
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  • 38. 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 09; 12(3):e1005941. PubMed ID: 27031109
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  • 39. 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 09; 1852(1):61-9. PubMed ID: 25463631
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  • 40. Molecular basis of erythroenzymopathies associated with hereditary hemolytic anemia: tabulation of mutant enzymes.
    Miwa S, Fujii H.
    Am J Hematol; 1996 Feb 09; 51(2):122-32. PubMed ID: 8579052
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