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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

152 related items for PubMed ID: 24192681

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  • 43. 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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  • 46. Differential effects on enzyme stability and kinetic parameters of mutants related to human triosephosphate isomerase deficiency.
    Cabrera N, Torres-Larios A, García-Torres I, Enríquez-Flores S, Perez-Montfort R.
    Biochim Biophys Acta Gen Subj; 2018 Jun; 1862(6):1401-1409. PubMed ID: 29571745
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  • 47. Hereditary triosephosphate isomerase (TPI) deficiency: two severely affected brothers one with and one without neurological symptoms.
    Hollán S, Fujii H, Hirono A, Hirono K, Karro H, Miwa S, Harsányi V, Gyódi E, Inselt-Kovács M.
    Hum Genet; 1993 Nov; 92(5):486-90. PubMed ID: 8244340
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  • 49. Congenital haemolytic anaemia resulting from glucose phosphate isomerase deficiency: genetics, clinical picture, and prenatal diagnosis.
    Whitelaw AG, Rogers PA, Hopkinson DA, Gordon H, Emerson PM, Darley JH, Reid C, Crawfurd MA.
    J Med Genet; 1979 Jun; 16(3):189-96. PubMed ID: 469896
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  • 50. Triose phosphate isomerase deficiency associated with two novel mutations in TPI gene.
    Fermo E, Bianchi P, Vercellati C, Rees DC, Marcello AP, Barcellini W, Zanella A.
    Eur J Haematol; 2010 Aug; 85(2):170-3. PubMed ID: 20374271
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  • 56. [Red cell enzyme deficiencies - clinical manifestation and pathophysiology (author's transl)].
    Gahr M.
    Monatsschr Kinderheilkd; 1981 Aug; 129(8):444-53. PubMed ID: 6116183
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  • 58. Prenatal diagnosis of a red-cell enzymopathy: triose phosphate isomerase deficiency.
    Bellingham AJ, Lestas AN, Williams LH, Nicolaides KH.
    Lancet; 1989 Aug 19; 2(8660):419-21. PubMed ID: 2569601
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