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Journal Abstract Search

264 related items for PubMed ID: 8922378

  • 1. 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; 135(4):939-51. PubMed ID: 8922378
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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
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  • 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
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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
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  • 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
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  • 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
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  • 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 09; 17(4):487-99. PubMed ID: 7967498
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  • 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
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