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PUBMED FOR HANDHELDS

Journal Abstract Search

240 related items for PubMed ID: 4152248

  • 21.
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  • 23. An enzymatic basis for a blood-brain barrier? The gamma-glutamyl cycle-background and considerations relating to amino acid transport in the brain.
    Meister A.
    Res Publ Assoc Res Nerv Ment Dis; 1974; 53():273-91. PubMed ID: 4155110
    [No Abstract] [Full Text] [Related]

  • 24.
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  • 25. Modulation of gamma-glutamyl cycle and glutathione levels in rat mammary gland explants.
    Puente J, Devoto MA, Sapag-Hagar M.
    Int J Tissue React; 1986; 8(2):105-10. PubMed ID: 2870991
    [Abstract] [Full Text] [Related]

  • 26. Regulation of gamma-glutamyl-cysteine synthetase by nonallosteric feedback inhibition by glutathione.
    Richman PG, Meister A.
    J Biol Chem; 1975 Feb 25; 250(4):1422-6. PubMed ID: 1112810
    [Abstract] [Full Text] [Related]

  • 27. Pyroglutamic aciduria: studies on the enzymic block and on the metabolic origin of pyroglutamic acid.
    Eldjarn L, Jellum E, Stokke O.
    Clin Chim Acta; 1972 Sep 25; 40(2):461-76. PubMed ID: 5056146
    [No Abstract] [Full Text] [Related]

  • 28. Erythrocyte glutathione synthetase in 5-oxoprolinuria: kinetic studies of the mutant enzyme and detection of heterozygotes.
    Larsson A, Zetterström R, Hörnell H, Porath U.
    Clin Chim Acta; 1976 Nov 15; 73(1):19-23. PubMed ID: 11905
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  • 30. Pyroglutamic aciduria (5-oxoprolinuria) without glutathione synthetase deficiency and with decreased pyroglutamate hydrolase activity.
    Roesel RA, Hommes FA, Samper L.
    J Inherit Metab Dis; 1981 Nov 15; 4(2):89-90. PubMed ID: 6790862
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  • 34. A newborn infant with generalized glutathione synthetase deficiency.
    Yapicioğlu H, Satar M, Tutak E, Narli N, Topaloğlu AK.
    Turk J Pediatr; 2004 Nov 15; 46(1):72-5. PubMed ID: 15074378
    [Abstract] [Full Text] [Related]

  • 35. Persistent 5-oxoprolinuria with normal glutathione synthase and 5-oxoprolinase activities.
    Ruijter GJ, Mourad-Baars PE, Ristoff E, Onkenhout W, Poorthuis BJ.
    J Inherit Metab Dis; 2006 Aug 15; 29(4):587. PubMed ID: 16830260
    [Abstract] [Full Text] [Related]

  • 36. Ophthalmological, psychometric and therapeutic investigation in two sisters with hereditary glutathione synthetase deficiency (5-oxoprolinuria).
    Larsson A, Wachtmeister L, von Wendt L, Andersson R, Hagenfeldt L, Herrin KM.
    Neuropediatrics; 1985 Aug 15; 16(3):131-6. PubMed ID: 4047346
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  • 38. Pyroglutamic aciduria in propionyl CoA carboxylase deficiency.
    Morishita H, Nagaya S, Nakajima T, Kawase A, Ohya A, Sugiyama S, Kamiya K, Watanabe I, Togari H, Suzuki Y.
    J Inherit Metab Dis; 1984 Aug 15; 7(3):139-40. PubMed ID: 6438400
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  • 39. Glutathione and related gamma-glutamyl compounds: biosynthesis and utilization.
    Meister A, Tate SS.
    Annu Rev Biochem; 1976 Aug 15; 45():559-604. PubMed ID: 9027
    [No Abstract] [Full Text] [Related]

  • 40. Enzymes of the gamma-glutamyl cycle in the ciliary body and lens.
    Ross LL, Barber L, Tate SS, Meister A.
    Proc Natl Acad Sci U S A; 1973 Aug 15; 70(8):2211-4. PubMed ID: 4152058
    [Abstract] [Full Text] [Related]

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