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Journal Abstract Search

261 related items for PubMed ID: 2925788

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. 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
    [Abstract] [Full Text] [Related]

  • 23. Peroxisomal and mitochondrial proliferation and increased alanine: glyoxylate aminotransferase activity in human liver after chlorpromazine-induced cholestasis.
    Cooper PJ, Danpure CJ, Simpson KJ.
    Biochem Soc Trans; 1989 Dec; 17(6):1071-2. PubMed ID: 2628084
    [No Abstract] [Full Text] [Related]

  • 24. Evolution of alanine:glyoxylate aminotransferase 1 peroxisomal and mitochondrial targeting. A survey of its subcellular distribution in the livers of various representatives of the classes Mammalia, Aves and Amphibia.
    Danpure CJ, Fryer P, Jennings PR, Allsop J, Griffiths S, Cunningham A.
    Eur J Cell Biol; 1994 Aug; 64(2):295-313. PubMed ID: 7813517
    [Abstract] [Full Text] [Related]

  • 25. Enzymatic heterogeneity in primary hyperoxaluria type 1 (hepatic peroxisomal alanine: glyoxylate aminotransferase deficiency).
    Danpure CJ, Jennings PR.
    J Inherit Metab Dis; 1988 Aug; 11 Suppl 2():205-7. PubMed ID: 3141703
    [No Abstract] [Full Text] [Related]

  • 26. 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
    [Abstract] [Full Text] [Related]

  • 27.
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  • 28. Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: a novel type of primary hyperoxaluria.
    Van Acker KJ, Eyskens FJ, Espeel MF, Wanders RJ, Dekker C, Kerckaert IO, Roels F.
    Kidney Int; 1996 Nov 15; 50(5):1747-52. PubMed ID: 8914045
    [Abstract] [Full Text] [Related]

  • 29.
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    [No Abstract] [Full Text] [Related]

  • 30. Molecular evolution of alanine/glyoxylate aminotransferase 1 intracellular targeting. Analysis of the feline gene.
    Lumb MJ, Purdue PE, Danpure CJ.
    Eur J Biochem; 1994 Apr 01; 221(1):53-62. PubMed ID: 8168541
    [Abstract] [Full Text] [Related]

  • 31. 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 Apr 01; 4(4):333-40. PubMed ID: 11156700
    [Abstract] [Full Text] [Related]

  • 32. Primary hyperoxaluria type 1: genotypic and phenotypic heterogeneity.
    Danpure CJ, Jennings PR, Fryer P, Purdue PE, Allsop J.
    J Inherit Metab Dis; 1994 Apr 01; 17(4):487-99. PubMed ID: 7967498
    [Abstract] [Full Text] [Related]

  • 33. Developmental profiles and properties of hepatic peroxisomal apo- and mitochondrial holoalanine:glyoxylate aminotransferase during chick embryogenesis.
    Noguchi T, Fujiwara S.
    J Biol Chem; 1984 Dec 10; 259(23):14498-504. PubMed ID: 6438098
    [Abstract] [Full Text] [Related]

  • 34. 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
    [Abstract] [Full Text] [Related]

  • 35.
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  • 36. Enzymological diagnosis of primary hyperoxaluria type 1 by measurement of hepatic alanine: glyoxylate aminotransferase activity.
    Danpure CJ, Jennings PR, Watts RW.
    Lancet; 1987 Feb 07; 1(8528):289-91. PubMed ID: 2880111
    [Abstract] [Full Text] [Related]

  • 37.
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  • 38. Targeting of alanine: glyoxylate aminotransferase in normal individuals and its mistargeting in patients with primary hyperoxaluria type 1.
    Danpure CJ, Jennings PR, Leiper JM, Lumb MJ, Oatey PB.
    Ann N Y Acad Sci; 1996 Dec 27; 804():477-90. PubMed ID: 8993566
    [No Abstract] [Full Text] [Related]

  • 39. Advances in the enzymology and molecular genetics of primary hyperoxaluria type 1. Prospects for gene therapy.
    Danpure CJ.
    Nephrol Dial Transplant; 1995 Dec 27; 10 Suppl 8():24-9. PubMed ID: 8592621
    [Abstract] [Full Text] [Related]

  • 40. Peroxisome localized human hepatic alanine-glyoxylate aminotransferase and its application to clinical diagnosis.
    Nakatani T, Kawasaki Y, Minatogawa Y, Okuno E, Kido R.
    Clin Biochem; 1985 Oct 27; 18(5):311-6. PubMed ID: 4053344
    [Abstract] [Full Text] [Related]

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