Similar articles for PMID: 1703535

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1

Identification of mutations associated with peroxisome-to-mitochondrion mistargeting of alanine/glyoxylate aminotransferase in primary hyperoxaluria type 1.

Purdue PE, Takada Y, Danpure CJ. Purdue PE, et al. J Cell Biol. 1990 Dec;111(6 Pt 1):2341-51. doi: 10.1083/jcb.111.6.2341. J Cell Biol. 1990. PMID: 1703535 Free PMC article.

2

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. Purdue PE, et al. Proc Natl Acad Sci U S A. 1991 Dec 1;88(23):10900-4. doi: 10.1073/pnas.88.23.10900. Proc Natl Acad Sci U S A. 1991. PMID: 1961759 Free PMC article.

3

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.

4

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. 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.

5

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. Leiper JM, et al. J Cell Biol. 1996 Nov;135(4):939-51. doi: 10.1083/jcb.135.4.939. J Cell Biol. 1996. PMID: 8922378 Free PMC article.

6

Alanine glyoxylate aminotransferase deficiency: biochemical and molecular genetic lessons from the study of a human disease.

Watts RW. Watts RW. Adv Enzyme Regul. 1992;32:309-27. doi: 10.1016/0065-2571(92)90024-t. Adv Enzyme Regul. 1992. PMID: 1496924 Review.

7

An intronic duplication in the alanine: glyoxylate aminotransferase gene facilitates identification of mutations in compound heterozygote patients with primary hyperoxaluria type 1.

Purdue PE, Lumb MJ, Allsop J, Danpure CJ. Purdue PE, et al. Hum Genet. 1991 Aug;87(4):394-6. doi: 10.1007/BF00197154. Hum Genet. 1991. PMID: 1879825

8

[Molecular pathology of type 1 primary hyperoxaluria].

Cochat P, Rolland MO, Bozon D, Dumontel C, Divry P. Cochat P, et al. Nephrologie. 1994;15(6):375-80. Nephrologie. 1994. PMID: 7862225 Review. French.

9

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.

10

A unique molecular basis for enzyme mistargeting in primary hyperoxaluria type 1.

Leiper JM, Danpure CJ. Leiper JM, et al. Clin Chim Acta. 1997 Oct 9;266(1):39-50. doi: 10.1016/s0009-8981(97)00165-4. Clin Chim Acta. 1997. PMID: 9435987

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