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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 [Abstract] [Full Text] [Related]
3. Primary hyperoxaluria type 1 and peroxisome-to-mitochondrion mistargeting of alanine:glyoxylate aminotransferase. Danpure CJ. Biochimie; 1993 Oct; 75(3-4):309-15. PubMed ID: 8507692 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
7. 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 01; 111(6 Pt 1):2341-51. PubMed ID: 1703535 [Abstract] [Full Text] [Related]
8. Alanine glyoxylate aminotransferase deficiency: biochemical and molecular genetic lessons from the study of a human disease. Watts RW. Adv Enzyme Regul; 1992 Dec 01; 32():309-27. PubMed ID: 1496924 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
11. Effect of N-terminal alpha-helix formation on the dimerization and intracellular targeting of alanine:glyoxylate aminotransferase. Lumb MJ, Drake AF, Danpure CJ. J Biol Chem; 1999 Jul 16; 274(29):20587-96. PubMed ID: 10400689 [Abstract] [Full Text] [Related]
12. 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 [Abstract] [Full Text] [Related]
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 15; 17(4):487-99. PubMed ID: 7967498 [Abstract] [Full Text] [Related]
14. Molecular evolution of alanine/glyoxylate aminotransferase 1 intracellular targeting. Analysis of the marmoset and rabbit genes. Purdue PE, Lumb MJ, Danpure CJ. Eur J Biochem; 1992 Jul 15; 207(2):757-66. PubMed ID: 1339350 [Abstract] [Full Text] [Related]
15. 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 [Abstract] [Full Text] [Related]
16. 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 15; 1763(12):1776-84. PubMed ID: 17027096 [Abstract] [Full Text] [Related]
17. Functional synergism between the most common polymorphism in human alanine:glyoxylate aminotransferase and four of the most common disease-causing mutations. Lumb MJ, Danpure CJ. J Biol Chem; 2000 Nov 17; 275(46):36415-22. PubMed ID: 10960483 [Abstract] [Full Text] [Related]
19. Correction of an enzyme trafficking defect in hereditary kidney stone disease in vitro. Lumb MJ, Birdsey GM, Danpure CJ. Biochem J; 2003 Aug 15; 374(Pt 1):79-87. PubMed ID: 12737622 [Abstract] [Full Text] [Related]
20. 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 [Abstract] [Full Text] [Related] Page: [Next] [New Search]