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PUBMED FOR HANDHELDS

Journal Abstract Search


212 related items for PubMed ID: 8244340

  • 61. 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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  • 62. A High-Content Screening Assay for Small Molecules That Stabilize Mutant Triose Phosphate Isomerase (TPI) as Treatments for TPI Deficiency.
    Vogt A, Eicher SL, Myers TD, Hrizo SL, Vollmer LL, Meyer EM, Palladino MJ.
    SLAS Discov; 2021 Sep 01; 26(8):1029-1039. PubMed ID: 34167376
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  • 63. Mild hemolytic anemia, progressive neuromotor retardation and fatal outcome: a disorder of glycolysis, triose- phosphate isomerase deficiency.
    Sarper N, Zengin E, Jakobs C, Salomons GS, Mc Wamelink M, Ralser M, Kurt K, Kara B.
    Turk J Pediatr; 2013 Sep 01; 55(2):198-202. PubMed ID: 24192681
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  • 64. Drosophila model of human inherited triosephosphate isomerase deficiency glycolytic enzymopathy.
    Celotto AM, Frank AC, Seigle JL, Palladino MJ.
    Genetics; 2006 Nov 01; 174(3):1237-46. PubMed ID: 16980388
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  • 67. Hereditary hemolytic anemia associated with glucosephosphate isomerase (GPI) deficiency--a new enzyme defect of human erythrocytes.
    Baughan MA, Valentine WN, Paglia DE, Ways PO, Simons ER, DeMarsh QB.
    Blood; 1968 Aug 01; 32(2):236-49. PubMed ID: 5672849
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  • 68. Triosephosphate isomerase deficiency: biochemical and molecular genetic analysis for prenatal diagnosis.
    Pekrun A, Neubauer BA, Eber SW, Lakomek M, Seidel H, Schröter W.
    Clin Genet; 1995 Apr 01; 47(4):175-9. PubMed ID: 7628118
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  • 73. Medical and Veterinary Importance of the Moonlighting Functions of Triosephosphate Isomerase.
    Rodríguez-Bolaños M, Perez-Montfort R.
    Curr Protein Pept Sci; 2019 Apr 01; 20(4):304-315. PubMed ID: 30370845
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  • 74. Cell proliferation-associated expression of a recently evolved isozyme of triosephosphate isomerase.
    Decker RS, Mohrenweiser HW.
    Biochem Genet; 1985 Apr 01; 23(3-4):267-80. PubMed ID: 4015618
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  • 75. Glutathione synthetase deficiency as a cause of hereditary hemolytic disease.
    Mohler DN, Majerus PW, Minnich V, Hess CE, Garrick MD.
    N Engl J Med; 1970 Dec 03; 283(23):1253-7. PubMed ID: 5476481
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  • 76. A mutation resulting in increased triosephosphate isomerase activity in Mus musculus.
    Merkle S, Reitmeir P, Pretsch W.
    Genet Res; 1991 Apr 03; 57(2):139-45. PubMed ID: 2055457
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  • 77. Red cell enzymopathies as a model of inborn errors of metabolism.
    Miwa S, Kanno H, Hirono A, Fujii H.
    Southeast Asian J Trop Med Public Health; 1995 Apr 03; 26 Suppl 1():112-9. PubMed ID: 8629088
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  • 79. The 1591C mutation in triosephosphate isomerase (TPI) deficiency. Tightly linked polymorphisms and a common haplotype in all known families.
    Schneider A, Westwood B, Yim C, Cohen-Solal M, Rosa R, Labotka R, Eber S, Wolf R, Lammi A, Beutler E.
    Blood Cells Mol Dis; 1996 Apr 03; 22(2):115-25. PubMed ID: 8931952
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