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254 related items for PubMed ID: 17027096

  • 1. 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; 1763(12):1776-84. PubMed ID: 17027096
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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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  • 3. Pharmacologic rescue of an enzyme-trafficking defect in primary hyperoxaluria 1.
    Miyata N, Steffen J, Johnson ME, Fargue S, Danpure CJ, Koehler CM.
    Proc Natl Acad Sci U S A; 2014 Oct 07; 111(40):14406-11. PubMed ID: 25237136
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  • 4. Molecular recognition of PTS-1 cargo proteins by Pex5p: implications for protein mistargeting in primary hyperoxaluria.
    Mesa-Torres N, Tomic N, Albert A, Salido E, Pey AL.
    Biomolecules; 2015 Feb 13; 5(1):121-41. PubMed ID: 25689234
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  • 9. 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 13; 53(2):417-32. PubMed ID: 8101040
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  • 11. Primary hyperoxaluria type 1 and peroxisome-to-mitochondrion mistargeting of alanine:glyoxylate aminotransferase.
    Danpure CJ.
    Biochimie; 1993 Aug 13; 75(3-4):309-15. PubMed ID: 8507692
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  • 12. 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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  • 14. 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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  • 15. Role of low native state kinetic stability and interaction of partially unfolded states with molecular chaperones in the mitochondrial protein mistargeting associated with primary hyperoxaluria.
    Pey AL, Salido E, Sanchez-Ruiz JM.
    Amino Acids; 2011 Nov 11; 41(5):1233-45. PubMed ID: 21103899
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  • 16. Primary hyperoxaluria type 1: genotypic and phenotypic heterogeneity.
    Danpure CJ, Jennings PR, Fryer P, Purdue PE, Allsop J.
    J Inherit Metab Dis; 1994 Nov 11; 17(4):487-99. PubMed ID: 7967498
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