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Journal Abstract Search

183 related items for PubMed ID: 3652453

  • 1. Alanine glyoxylate aminotransferase and the urinary excretion of oxalate and glycollate in hyperoxaluria type I and the Zellweger syndrome.
    Wanders RJ, van Roermund CW, Westra R, Schutgens RB, van der Ende MA, Tager JM, Monnens LA, Baadenhuysen H, Govaerts L, Przyrembel H.
    Clin Chim Acta; 1987 Jun 15; 165(2-3):311-9. PubMed ID: 3652453
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  • 2. Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I.
    Danpure CJ, Jennings PR.
    FEBS Lett; 1986 May 26; 201(1):20-4. PubMed ID: 3709805
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  • 3. Cytosolic compartmentalization of hepatic alanine:glyoxylate aminotransferase in patients with aberrant peroxisomal biogenesis and its effect on oxalate metabolism.
    Danpure CJ, Fryer P, Griffiths S, Guttridge KM, Jennings PR, Allsop J, Moser AB, Naidu S, Moser HW, MacCollin M.
    J Inherit Metab Dis; 1994 May 26; 17(1):27-40. PubMed ID: 8051936
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  • 4. Diversity in residual alanine glyoxylate aminotransferase activity in hyperoxaluria type I: correlation with pyridoxine responsiveness.
    Wanders RJ, van Roermund CW, Jurriaans S, Schutgens RB, Tager JM, van den Bosch H, Wolff ED, Przyrembel H, Berger R, Schaaphok FG.
    J Inherit Metab Dis; 1988 May 26; 11 Suppl 2():208-11. PubMed ID: 3141704
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  • 5. High incidence of hyperoxaluria in generalized peroxisomal disorders.
    van Woerden CS, Groothoff JW, Wijburg FA, Duran M, Wanders RJ, Barth PG, Poll-The BT.
    Mol Genet Metab; 2006 Aug 26; 88(4):346-50. PubMed ID: 16621644
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  • 6. Enzymatic heterogeneity in primary hyperoxaluria type 1 (hepatic peroxisomal alanine: glyoxylate aminotransferase deficiency).
    Danpure CJ, Jennings PR.
    J Inherit Metab Dis; 1988 Aug 26; 11 Suppl 2():205-7. PubMed ID: 3141703
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  • 7. Further studies on the activity and subcellular distribution of alanine:glyoxylate aminotransferase in the livers of patients with primary hyperoxaluria type 1.
    Danpure CJ, Jennings PR.
    Clin Sci (Lond); 1988 Sep 26; 75(3):315-22. PubMed ID: 3416563
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  • 8. Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: a novel type of primary hyperoxaluria.
    Van Acker KJ, Eyskens FJ, Espeel MF, Wanders RJ, Dekker C, Kerckaert IO, Roels F.
    Kidney Int; 1996 Nov 26; 50(5):1747-52. PubMed ID: 8914045
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  • 14. Mammalian alanine/glyoxylate aminotransferase 1 is imported into peroxisomes via the PTS1 translocation pathway. Increased degeneracy and context specificity of the mammalian PTS1 motif and implications for the peroxisome-to-mitochondrion mistargeting of AGT in primary hyperoxaluria type 1.
    Motley A, Lumb MJ, Oatey PB, Jennings PR, De Zoysa PA, Wanders RJ, Tabak HF, Danpure CJ.
    J Cell Biol; 1995 Oct 26; 131(1):95-109. PubMed ID: 7559790
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  • 16. Fetal liver alanine: glyoxylate aminotransferase and the prenatal diagnosis of primary hyperoxaluria type 1.
    Danpure CJ, Jennings PR, Penketh RJ, Wise PJ, Cooper PJ, Rodeck CH.
    Prenat Diagn; 1989 Apr 26; 9(4):271-81. PubMed ID: 2717533
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  • 17. ATP-dependent degradation of a mutant serine: pyruvate/alanine:glyoxylate aminotransferase in a primary hyperoxaluria type 1 case.
    Nishiyama K, Funai T, Yokota S, Ichiyama A.
    J Cell Biol; 1993 Dec 26; 123(5):1237-48. PubMed ID: 8245128
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  • 18. Molecular and clinical heterogeneity in primary hyperoxaluria type 1.
    Danpure CJ.
    Am J Kidney Dis; 1991 Apr 26; 17(4):366-9. PubMed ID: 2008900
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  • 20. Plasma and urine glycolate assays for differentiating the hyperoxaluria syndromes.
    Marangella M, Petrarulo M, Vitale C, Cosseddu D, Linari F.
    J Urol; 1992 Sep 26; 148(3 Pt 2):986-9. PubMed ID: 1507356
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