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Journal Abstract Search

187 related items for PubMed ID: 7315100

  • 1. The role of enzyme variants, polymorphisms and enzyme hybrids in enzyme deficiency conditions.
    Aebi H, Wyss SR.
    Acta Biol Med Ger; 1981; 40(4-5):537-41. PubMed ID: 7315100
    [Abstract] [Full Text] [Related]

  • 2. Unstable mutants and molecular hybrids in enzyme deficiency conditions.
    Aebi H, Wyss SR, Scherz B.
    Acta Biol Med Ger; 1977; 36(5-6):735-41. PubMed ID: 602579
    [Abstract] [Full Text] [Related]

  • 3. New stable mutant (Gd(-) variants: G6PD Tashkent and G6PD Nucus. Molecular basis of hereditary enzyme deficiency.
    Yermakov N, Tokarev Ju, Chernjak N, Schönian G, Grieger M, Guckler A, Jacobasch G, Mahmudova M, Bahramov S.
    Acta Biol Med Ger; 1981; 40(4-5):559-62. PubMed ID: 7315103
    [Abstract] [Full Text] [Related]

  • 4. Heterogeneity of glucose-6-phosphate dehydrogenase enzymopathies in the GDR.
    Jacobasch G, Buckwitz D, Jurowski R, Gerth C, Plonka A, Kuckelkorn U.
    Biomed Biochim Acta; 1987; 46(2-3):S177-81. PubMed ID: 3593296
    [Abstract] [Full Text] [Related]

  • 5. Heterogeneity of red cell glucose-6-phosphate dehydrogenase (G-6-PD) deficiency in Egypt.
    McCurdy PR, Kamel K, Selim O.
    J Lab Clin Med; 1974 Nov; 84(5):673-80. PubMed ID: 4283789
    [No Abstract] [Full Text] [Related]

  • 6. Structural variants of human glucose 6-phosphate dehydrogenase (G6PD): role of intracellular decay in the expression of deficiency.
    De Flora A, Morelli A, Benatti U.
    Biomed Biochim Acta; 1983 Nov; 42(11-12):S247-52. PubMed ID: 6675698
    [Abstract] [Full Text] [Related]

  • 7. Properties of erythrocyte catalase from heterozygotes for Japanese type acatalasemia.
    Ogata M, Mizugaki J.
    Acta Med Okayama; 1979 Jun; 33(3):205-11. PubMed ID: 40400
    [Abstract] [Full Text] [Related]

  • 8. [Glucose-6-phosphate dehydrogenase deficiency of erythrocytes in the GDR].
    Guckler A, Grieger M, Jacobasch G, Bier K.
    Acta Biol Med Ger; 1977 Jun; 36(5-6):765-71. PubMed ID: 23636
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  • 10. [Detection of female heterozygous glucose-6-phosphate dehydrogenase deficiency].
    Grieger M, Jacobasch G.
    Acta Biol Med Ger; 1977 Jun; 36(5-6):773-7. PubMed ID: 23637
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  • 13. Red cell glucose-6-phosphate dehydrogenase phenotypes in Iraq.
    Hilmi FA, Al-Allawi NA, Rassam M, Al-Shamma G, Al-Hashimi A.
    East Mediterr Health J; 2002 Jan; 8(1):42-8. PubMed ID: 15330559
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  • 16. Molecular basis of G6PD deficiency in India.
    Sukumar S, Mukherjee MB, Colah RB, Mohanty D.
    Blood Cells Mol Dis; 2004 Jan; 33(2):141-5. PubMed ID: 15315792
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  • 17. 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 Jan; 26 Suppl 1():112-9. PubMed ID: 8629088
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  • 19. [Attempt at characterization of 2 erythrocyte variants of glucose-6-phosphate dehydrogenase in a patient with a partial enzymatic deficit].
    Bansard-Desmidt N.
    Biomedicine; 1975 Sep; 22(5):411-5. PubMed ID: 1222212
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