Danpure CJ - Search Results

1

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. Danpure CJ, et al. J Cell Biol. 1989 Apr;108(4):1345-52. doi: 10.1083/jcb.108.4.1345. J Cell Biol. 1989. PMID: 2925788 Free PMC article.

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. Motley A, et al. Among authors: danpure cj. J Cell Biol. 1995 Oct;131(1):95-109. doi: 10.1083/jcb.131.1.95. J Cell Biol. 1995. PMID: 7559790 Free PMC article.

3

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. Danpure CJ, et al. Eur J Cell Biol. 1994 Aug;64(2):295-313. Eur J Cell Biol. 1994. PMID: 7813517

4

Primary hyperoxaluria type 1: genotypic and phenotypic heterogeneity.

Danpure CJ, Jennings PR, Fryer P, Purdue PE, Allsop J. Danpure CJ, et al. J Inherit Metab Dis. 1994;17(4):487-99. doi: 10.1007/BF00711363. J Inherit Metab Dis. 1994. PMID: 7967498 Review.

5

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, et al. Danpure CJ, et al. J Inherit Metab Dis. 1994;17(1):27-40. doi: 10.1007/BF00735393. J Inherit Metab Dis. 1994. PMID: 8051936

6

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, et al. Danpure CJ, et al. Am J Hum Genet. 1993 Aug;53(2):417-32. Am J Hum Genet. 1993. PMID: 8101040 Free PMC article.

7

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. Danpure CJ, et al. Ann N Y Acad Sci. 1996 Dec 27;804:477-90. doi: 10.1111/j.1749-6632.1996.tb18638.x. Ann N Y Acad Sci. 1996. PMID: 8993566 No abstract available.

8

Enzymological characterization of a putative canine analogue of primary hyperoxaluria type 1.

Danpure CJ, Jennings PR, Jansen JH. Danpure CJ, et al. Biochim Biophys Acta. 1991 Feb 22;1096(2):134-8. doi: 10.1016/0925-4439(91)90051-a. Biochim Biophys Acta. 1991. PMID: 1672096

9

Subcellular distribution of hepatic alanine:glyoxylate aminotransferase in various mammalian species.

Danpure CJ, Guttridge KM, Fryer P, Jennings PR, Allsop J, Purdue PE. Danpure CJ, et al. J Cell Sci. 1990 Dec;97 ( Pt 4):669-78. doi: 10.1242/jcs.97.4.669. J Cell Sci. 1990. PMID: 2127597

10

Immunological heterogeneity of hepatic alanine:glyoxylate aminotransferase in primary hyperoxaluria type 1.

Wise PJ, Danpure CJ, Jennings PR. Wise PJ, et al. Among authors: danpure cj. FEBS Lett. 1987 Sep 28;222(1):17-20. doi: 10.1016/0014-5793(87)80183-7. FEBS Lett. 1987. PMID: 2443389 Free article.

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