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Journal Abstract Search

264 related items for PubMed ID: 8922378

  • 1.
    ; . PubMed ID:
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  • 2. 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; 131(1):95-109. PubMed ID: 7559790
    [Abstract] [Full Text] [Related]

  • 3. Primary hyperoxaluria type 1 and peroxisome-to-mitochondrion mistargeting of alanine:glyoxylate aminotransferase.
    Danpure CJ.
    Biochimie; 1993 Oct; 75(3-4):309-15. PubMed ID: 8507692
    [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.
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  • 6. The molecular basis of alanine: glyoxylate aminotransferase mistargeting: the most common single cause of primary hyperoxaluria type 1.
    Danpure CJ.
    J Nephrol; 1998 Dec 01; 11 Suppl 1():8-12. PubMed ID: 9604801
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Alanine glyoxylate aminotransferase deficiency: biochemical and molecular genetic lessons from the study of a human disease.
    Watts RW.
    Adv Enzyme Regul; 1992 Dec 01; 32():309-27. PubMed ID: 1496924
    [Abstract] [Full Text] [Related]

  • 9. Variable peroxisomal and mitochondrial targeting of alanine: glyoxylate aminotransferase in mammalian evolution and disease.
    Danpure CJ.
    Bioessays; 1997 Apr 01; 19(4):317-26. PubMed ID: 9136629
    [Abstract] [Full Text] [Related]

  • 10. A unique molecular basis for enzyme mistargeting in primary hyperoxaluria type 1.
    Leiper JM, Danpure CJ.
    Clin Chim Acta; 1997 Oct 09; 266(1):39-50. PubMed ID: 9435987
    [Abstract] [Full Text] [Related]

  • 11. Effect of N-terminal alpha-helix formation on the dimerization and intracellular targeting of alanine:glyoxylate aminotransferase.
    Lumb MJ, Drake AF, Danpure CJ.
    J Biol Chem; 1999 Jul 16; 274(29):20587-96. PubMed ID: 10400689
    [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. Primary hyperoxaluria type 1: genotypic and phenotypic heterogeneity.
    Danpure CJ, Jennings PR, Fryer P, Purdue PE, Allsop J.
    J Inherit Metab Dis; 1994 Oct 15; 17(4):487-99. PubMed ID: 7967498
    [Abstract] [Full Text] [Related]

  • 14. Molecular evolution of alanine/glyoxylate aminotransferase 1 intracellular targeting. Analysis of the marmoset and rabbit genes.
    Purdue PE, Lumb MJ, Danpure CJ.
    Eur J Biochem; 1992 Jul 15; 207(2):757-66. PubMed ID: 1339350
    [Abstract] [Full Text] [Related]

  • 15. 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 15; 123(5):1237-48. PubMed ID: 8245128
    [Abstract] [Full Text] [Related]

  • 16. Primary hyperoxaluria type 1: AGT mistargeting highlights the fundamental differences between the peroxisomal and mitochondrial protein import pathways.
    Danpure CJ.
    Biochim Biophys Acta; 2006 Dec 15; 1763(12):1776-84. PubMed ID: 17027096
    [Abstract] [Full Text] [Related]

  • 17. Functional synergism between the most common polymorphism in human alanine:glyoxylate aminotransferase and four of the most common disease-causing mutations.
    Lumb MJ, Danpure CJ.
    J Biol Chem; 2000 Nov 17; 275(46):36415-22. PubMed ID: 10960483
    [Abstract] [Full Text] [Related]

  • 18. Alanine:glyoxylate aminotransferase peroxisome-to-mitochondrion mistargeting in human hereditary kidney stone disease.
    Danpure CJ, Lumb MJ, Birdsey GM, Zhang X.
    Biochim Biophys Acta; 2003 Apr 11; 1647(1-2):70-5. PubMed ID: 12686111
    [Abstract] [Full Text] [Related]

  • 19. Correction of an enzyme trafficking defect in hereditary kidney stone disease in vitro.
    Lumb MJ, Birdsey GM, Danpure CJ.
    Biochem J; 2003 Aug 15; 374(Pt 1):79-87. PubMed ID: 12737622
    [Abstract] [Full Text] [Related]

  • 20. 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 15; 36(10):1285-94. PubMed ID: 3418107
    [Abstract] [Full Text] [Related]

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