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261 related items for PubMed ID: 2925788

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Mistargeting of peroxisomal L-alanine:glyoxylate aminotransferase to mitochondria in primary hyperoxaluria patients depends upon activation of a cryptic mitochondrial targeting sequence by a point mutation.
    Purdue PE, Allsop J, Isaya G, Rosenberg LE, Danpure CJ.
    Proc Natl Acad Sci U S A; 1991 Dec 01; 88(23):10900-4. PubMed ID: 1961759
    [Abstract] [Full Text] [Related]

  • 5. Identification of mutations associated with peroxisome-to-mitochondrion mistargeting of alanine/glyoxylate aminotransferase in primary hyperoxaluria type 1.
    Purdue PE, Takada Y, Danpure CJ.
    J Cell Biol; 1990 Dec 01; 111(6 Pt 1):2341-51. PubMed ID: 1703535
    [Abstract] [Full Text] [Related]

  • 6. Enzymological and mutational analysis of a complex primary hyperoxaluria type 1 phenotype involving alanine:glyoxylate aminotransferase peroxisome-to-mitochondrion mistargeting and intraperoxisomal aggregation.
    Danpure CJ, Purdue PE, Fryer P, Griffiths S, Allsop J, Lumb MJ, Guttridge KM, Jennings PR, Scheinman JI, Mauer SM.
    Am J Hum Genet; 1993 Aug 01; 53(2):417-32. PubMed ID: 8101040
    [Abstract] [Full Text] [Related]

  • 7. 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 01; 131(1):95-109. PubMed ID: 7559790
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10.
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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
    [Abstract] [Full Text] [Related]

  • 12. Molecular basis of the variable mitochondrial and peroxisomal localisation of alanine-glyoxylate aminotransferase.
    Oatey PB, Lumb MJ, Danpure CJ.
    Eur J Biochem; 1996 Oct 15; 241(2):374-85. PubMed ID: 8917433
    [Abstract] [Full Text] [Related]

  • 13. Subcellular distribution of hepatic alanine:glyoxylate aminotransferase in various mammalian species.
    Danpure CJ, Guttridge KM, Fryer P, Jennings PR, Allsop J, Purdue PE.
    J Cell Sci; 1990 Dec 15; 97 ( Pt 4)():669-78. PubMed ID: 2127597
    [Abstract] [Full Text] [Related]

  • 14. [Molecular pathology of type 1 primary hyperoxaluria].
    Cochat P, Rolland MO, Bozon D, Dumontel C, Divry P.
    Nephrologie; 1994 Dec 15; 15(6):375-80. PubMed ID: 7862225
    [Abstract] [Full Text] [Related]

  • 15. Immunological heterogeneity of hepatic alanine:glyoxylate aminotransferase in primary hyperoxaluria type 1.
    Wise PJ, Danpure CJ, Jennings PR.
    FEBS Lett; 1987 Sep 28; 222(1):17-20. PubMed ID: 2443389
    [Abstract] [Full Text] [Related]

  • 16. Variable peroxisomal and mitochondrial targeting of alanine: glyoxylate aminotransferase in mammalian evolution and disease.
    Danpure CJ.
    Bioessays; 1997 Apr 28; 19(4):317-26. PubMed ID: 9136629
    [Abstract] [Full Text] [Related]

  • 17. 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 28; 9(4):271-81. PubMed ID: 2717533
    [Abstract] [Full Text] [Related]

  • 18. Purification and characterization of peroxisomal apo and holo alanine:glyoxylate aminotransferase from bird liver.
    Sakuraba H, Fujiwara S, Noguchi T.
    Arch Biochem Biophys; 1991 May 01; 286(2):453-60. PubMed ID: 1654790
    [Abstract] [Full Text] [Related]

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  • 20. Primary hyperoxaluria type 1 and peroxisome-to-mitochondrion mistargeting of alanine:glyoxylate aminotransferase.
    Danpure CJ.
    Biochimie; 1993 May 01; 75(3-4):309-15. PubMed ID: 8507692
    [Abstract] [Full Text] [Related]

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