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Journal Abstract Search

166 related items for PubMed ID: 8051936

  • 1. Cytosolic compartmentalization of hepatic alanine:glyoxylate aminotransferase in patients with aberrant peroxisomal biogenesis and its effect on oxalate metabolism.
    Danpure CJ, Fryer P, Griffiths S, Guttridge KM, Jennings PR, Allsop J, Moser AB, Naidu S, Moser HW, MacCollin M.
    J Inherit Metab Dis; 1994; 17(1):27-40. PubMed ID: 8051936
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  • 2. Alanine glyoxylate aminotransferase and the urinary excretion of oxalate and glycollate in hyperoxaluria type I and the Zellweger syndrome.
    Wanders RJ, van Roermund CW, Westra R, Schutgens RB, van der Ende MA, Tager JM, Monnens LA, Baadenhuysen H, Govaerts L, Przyrembel H.
    Clin Chim Acta; 1987 Jun 15; 165(2-3):311-9. PubMed ID: 3652453
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  • 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 15; 36(10):1285-94. PubMed ID: 3418107
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  • 6. 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 15; 108(4):1345-52. PubMed ID: 2925788
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  • 8. Alanine glyoxylate aminotransferase deficiency: biochemical and molecular genetic lessons from the study of a human disease.
    Watts RW.
    Adv Enzyme Regul; 1992 Apr 15; 32():309-27. PubMed ID: 1496924
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  • 9. 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 15; 111(6 Pt 1):2341-51. PubMed ID: 1703535
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  • 10. 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 15; 53(2):417-32. PubMed ID: 8101040
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  • 11. The effect of vitamin B6 deficiency on alanine: glyoxylate aminotransferase isoenzymes in rat liver.
    Takada Y, Mori T, Noguchi T.
    Arch Biochem Biophys; 1984 Feb 15; 229(1):1-6. PubMed ID: 6703688
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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 15; 123(5):1237-48. PubMed ID: 8245128
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  • 13. Oxalate synthesis in mammals: properties and subcellular distribution of serine:pyruvate/alanine:glyoxylate aminotransferase in the liver.
    Ichiyama A, Xue HH, Oda T, Uchida C, Sugiyama T, Maeda-Nakai E, Sato K, Nagai E, Watanabe S, Takayama T.
    Mol Urol; 2000 Dec 15; 4(4):333-40. PubMed ID: 11156700
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  • 14. 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
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  • 15. Molecular and clinical heterogeneity in primary hyperoxaluria type 1.
    Danpure CJ.
    Am J Kidney Dis; 1991 Apr 15; 17(4):366-9. PubMed ID: 2008900
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  • 16. Molecular Insight into the Synergism between the Minor Allele of Human Liver Peroxisomal Alanine:Glyoxylate Aminotransferase and the F152I Mutation.
    Cellini B, Montioli R, Paiardini A, Lorenzetto A, Voltattorni CB.
    J Biol Chem; 2009 Mar 27; 284(13):8349-58. PubMed ID: 19155213
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  • 17. 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 27; 135(4):939-51. PubMed ID: 8922378
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  • 19. Primary hyperoxaluria type 1 and peroxisome-to-mitochondrion mistargeting of alanine:glyoxylate aminotransferase.
    Danpure CJ.
    Biochimie; 1993 Nov 27; 75(3-4):309-15. PubMed ID: 8507692
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  • 20. High incidence of hyperoxaluria in generalized peroxisomal disorders.
    van Woerden CS, Groothoff JW, Wijburg FA, Duran M, Wanders RJ, Barth PG, Poll-The BT.
    Mol Genet Metab; 2006 Aug 27; 88(4):346-50. PubMed ID: 16621644
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