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272 related items for PubMed ID: 3416563

  • 1. 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; 75(3):315-22. PubMed ID: 3416563
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  • 2. Immunocytochemical localization of human hepatic alanine: glyoxylate aminotransferase in control subjects and patients with primary hyperoxaluria type 1.
    Cooper PJ, Danpure CJ, Wise PJ, Guttridge KM.
    J Histochem Cytochem; 1988 Oct; 36(10):1285-94. PubMed ID: 3418107
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  • 3. An enzyme trafficking defect in two patients with primary hyperoxaluria type 1: peroxisomal alanine/glyoxylate aminotransferase rerouted to mitochondria.
    Danpure CJ, Cooper PJ, Wise PJ, Jennings PR.
    J Cell Biol; 1989 Apr; 108(4):1345-52. PubMed ID: 2925788
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  • 7. Enzymological diagnosis of primary hyperoxaluria type 1 by measurement of hepatic alanine: glyoxylate aminotransferase activity.
    Danpure CJ, Jennings PR, Watts RW.
    Lancet; 1987 Feb 07; 1(8528):289-91. PubMed ID: 2880111
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  • 9. 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 07; 131(1):95-109. PubMed ID: 7559790
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  • 10. 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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  • 11. Inhibition of alanine:glyoxylate aminotransferase 1 dimerization is a prerequisite for its peroxisome-to-mitochondrion mistargeting in primary hyperoxaluria type 1.
    Leiper JM, Oatey PB, Danpure CJ.
    J Cell Biol; 1996 Nov 26; 135(4):939-51. PubMed ID: 8922378
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  • 12. 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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  • 14. Gly161 mutations associated with Primary Hyperoxaluria Type I induce the cytosolic aggregation and the intracellular degradation of the apo-form of alanine:glyoxylate aminotransferase.
    Oppici E, Roncador A, Montioli R, Bianconi S, Cellini B.
    Biochim Biophys Acta; 2013 Dec 26; 1832(12):2277-88. PubMed ID: 24055001
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  • 18. Effects of alanine:glyoxylate aminotransferase variants and pyridoxine sensitivity on oxalate metabolism in a cell-based cytotoxicity assay.
    Fargue S, Knight J, Holmes RP, Rumsby G, Danpure CJ.
    Biochim Biophys Acta; 2016 Jun 26; 1862(6):1055-62. PubMed ID: 26854734
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