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Journal Abstract Search


127 related items for PubMed ID: 907660

  • 21. First trimester studies of a fetus at risk for triose phosphate isomerase deficiency.
    Dallapiccola B, Novelli G, Cuoco C, Porro E.
    Prenat Diagn; 1987 May; 7(4):289-94. PubMed ID: 3588545
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  • 23. Elevated frequency of carriers for triosephosphate isomerase deficiency in newborn infants.
    Mohrenweiser HW, Fielek S.
    Pediatr Res; 1982 Nov; 16(11):960-3. PubMed ID: 7155666
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  • 24. An allele at the triose phosphate isomerase, Tpi-1 locus on chromosome 6 recovered from feral mice.
    Bulfield G, Ball ST, Peters J.
    Genet Res; 1987 Dec; 50(3):239-43. PubMed ID: 3443296
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  • 26. Characterization of three electrophoretic variants of human erythrocyte triosephosphate isomerase found in Japanese.
    Asakawa J, Satoh C.
    Biochem Genet; 1986 Feb; 24(1-2):131-48. PubMed ID: 3964229
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  • 28. Purification, crystallization and properties of triosephosphate isomerase from human skeletal muscle.
    Dabrowska A, Kamrowska I, Baranowski T.
    Acta Biochim Pol; 1978 Feb; 25(3):247-56. PubMed ID: 752201
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  • 30. Myopathy with altered mitochondria due to a triosephosphate isomerase (TPI) deficiency.
    Bardosi A, Eber SW, Hendrys M, Pekrun A.
    Acta Neuropathol; 1990 Feb; 79(4):387-94. PubMed ID: 2339591
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  • 31. Characterization of two new electrophoretic variants of human triosephosphate isomerase: stability, kinetic, and immunological properties.
    Asakawa J, Mohrenweiser HW.
    Biochem Genet; 1982 Feb; 20(1-2):59-76. PubMed ID: 7092803
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  • 33. Triosephosphate isomerase from human and horse liver.
    Snyder R, Lee EW.
    Methods Enzymol; 1975 Feb; 41():430-4. PubMed ID: 1168838
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  • 34. A preliminary study of the electrophoresis of nucleoside phosphorylase, 2,3-diphosphoglycerate mutase, triosephosphate isomerase and galctose-1-uridyle transferase: technical notes.
    Kishimoto S, Iwasaki Y, Tsuchihashi Y, Daitoku K, Yamada T.
    Hiroshima J Med Sci; 1976 Mar; 25(1):63-72. PubMed ID: 135747
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  • 37. Human triose-phosphate isomerase deficiency: a single amino acid substitution results in a thermolabile enzyme.
    Daar IO, Artymiuk PJ, Phillips DC, Maquat LE.
    Proc Natl Acad Sci U S A; 1986 Oct; 83(20):7903-7. PubMed ID: 2876430
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  • 38. Thermostability characteristics of glucosephosphate and triosephosphate isomerase in erythrocytes from several species.
    Naidu JM, Turner TR, Mohrenweiser HW.
    Comp Biochem Physiol B; 1984 Oct; 79(2):211-7. PubMed ID: 6509914
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  • 39. Origin of the triosephosphate isomerase isozymes in humans: genetic evidence for the expression of a single structural locus.
    Decker RS, Mohrenweiser HW.
    Am J Hum Genet; 1981 Sep; 33(5):683-91. PubMed ID: 7294020
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  • 40. Origin of human triosephosphate isomerase isozymes: further evidence for the single structural locus hypothesis with Japanese variants.
    Asakawa J, Iida S.
    Hum Genet; 1985 Sep; 71(1):22-6. PubMed ID: 3861565
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