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Journal Abstract Search

287 related items for PubMed ID: 3418107

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  • 3. Fetal liver alanine: glyoxylate aminotransferase and the prenatal diagnosis of primary hyperoxaluria type 1.
    Danpure CJ, Jennings PR, Penketh RJ, Wise PJ, Cooper PJ, Rodeck CH.
    Prenat Diagn; 1989 Apr; 9(4):271-81. PubMed ID: 2717533
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  • 5. Immunological heterogeneity of hepatic alanine:glyoxylate aminotransferase in primary hyperoxaluria type 1.
    Wise PJ, Danpure CJ, Jennings PR.
    FEBS Lett; 1987 Sep 28; 222(1):17-20. PubMed ID: 2443389
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  • 6. Alanine glyoxylate aminotransferase deficiency: biochemical and molecular genetic lessons from the study of a human disease.
    Watts RW.
    Adv Enzyme Regul; 1992 Sep 28; 32():309-27. PubMed ID: 1496924
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  • 8. 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 28; 53(2):417-32. PubMed ID: 8101040
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  • 11. 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 28; 135(4):939-51. PubMed ID: 8922378
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  • 12. 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 28; 111(6 Pt 1):2341-51. PubMed ID: 1703535
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  • 13. The molecular basis of alanine: glyoxylate aminotransferase mistargeting: the most common single cause of primary hyperoxaluria type 1.
    Danpure CJ.
    J Nephrol; 1998 Dec 28; 11 Suppl 1():8-12. PubMed ID: 9604801
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  • 14. Gly161 mutations associated with Primary Hyperoxaluria Type I induce the cytosolic aggregation and the intracellular degradation of the apo-form of alanine:glyoxylate aminotransferase.
    Oppici E, Roncador A, Montioli R, Bianconi S, Cellini B.
    Biochim Biophys Acta; 2013 Dec 28; 1832(12):2277-88. PubMed ID: 24055001
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  • 15. [Molecular pathology of type 1 primary hyperoxaluria].
    Cochat P, Rolland MO, Bozon D, Dumontel C, Divry P.
    Nephrologie; 1994 Dec 28; 15(6):375-80. PubMed ID: 7862225
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  • 16. Primary hyperoxaluria type 1 and peroxisome-to-mitochondrion mistargeting of alanine:glyoxylate aminotransferase.
    Danpure CJ.
    Biochimie; 1993 Dec 28; 75(3-4):309-15. PubMed ID: 8507692
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  • 17. Primary hyperoxaluria type 1: genotypic and phenotypic heterogeneity.
    Danpure CJ, Jennings PR, Fryer P, Purdue PE, Allsop J.
    J Inherit Metab Dis; 1994 Dec 28; 17(4):487-99. PubMed ID: 7967498
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  • 18. 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 28; 1763(12):1776-84. PubMed ID: 17027096
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  • 19. 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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  • 20. A new micro-assay for human liver alanine: glyoxylate aminotransferase.
    Allsop J, Jennings PR, Danpure CJ.
    Clin Chim Acta; 1987 Dec 01; 170(2-3):187-93. PubMed ID: 3436053
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