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2. Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I. Danpure CJ; Jennings PR FEBS Lett; 1986 May; 201(1):20-4. PubMed ID: 3709805 [TBL] [Abstract][Full Text] [Related]
3. Diversity in residual alanine glyoxylate aminotransferase activity in hyperoxaluria type I: correlation with pyridoxine responsiveness. Wanders RJ; van Roermund CW; Jurriaans S; Schutgens RB; Tager JM; van den Bosch H; Wolff ED; Przyrembel H; Berger R; Schaaphok FG J Inherit Metab Dis; 1988; 11 Suppl 2():208-11. PubMed ID: 3141704 [No Abstract] [Full Text] [Related]
4. Immunological heterogeneity of hepatic alanine:glyoxylate aminotransferase in primary hyperoxaluria type 1. Wise PJ; Danpure CJ; Jennings PR FEBS Lett; 1987 Sep; 222(1):17-20. PubMed ID: 2443389 [TBL] [Abstract][Full Text] [Related]
5. 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; 36(10):1285-94. PubMed ID: 3418107 [TBL] [Abstract][Full Text] [Related]
6. Successful treatment of primary hyperoxaluria type I by combined hepatic and renal transplantation. Watts RW; Calne RY; Rolles K; Danpure CJ; Morgan SH; Mansell MA; Williams R; Purkiss P Lancet; 1987 Aug; 2(8557):474-5. PubMed ID: 2887776 [TBL] [Abstract][Full Text] [Related]
7. 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 J Cell Biol; 1989 Apr; 108(4):1345-52. PubMed ID: 2925788 [TBL] [Abstract][Full Text] [Related]
8. Alanine glyoxylate aminotransferase and the urinary excretion of oxalate and glycollate in hyperoxaluria type I and the Zellweger syndrome. Wanders RJ; van Roermund CW; Westra R; Schutgens RB; van der Ende MA; Tager JM; Monnens LA; Baadenhuysen H; Govaerts L; Przyrembel H Clin Chim Acta; 1987 Jun; 165(2-3):311-9. PubMed ID: 3652453 [TBL] [Abstract][Full Text] [Related]
9. A new micro-assay for human liver alanine: glyoxylate aminotransferase. Allsop J; Jennings PR; Danpure CJ Clin Chim Acta; 1987 Dec; 170(2-3):187-93. PubMed ID: 3436053 [TBL] [Abstract][Full Text] [Related]
10. [Molecular pathology of type 1 primary hyperoxaluria]. Cochat P; Rolland MO; Bozon D; Dumontel C; Divry P Nephrologie; 1994; 15(6):375-80. PubMed ID: 7862225 [TBL] [Abstract][Full Text] [Related]
11. Alanine glyoxylate aminotransferase deficiency: biochemical and molecular genetic lessons from the study of a human disease. Watts RW Adv Enzyme Regul; 1992; 32():309-27. PubMed ID: 1496924 [TBL] [Abstract][Full Text] [Related]
12. 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; 229(1):1-6. PubMed ID: 6703688 [TBL] [Abstract][Full Text] [Related]
13. Enzyme deficiency for type 1 primary hyperoxaluria. Small KW Arch Ophthalmol; 1992 Jan; 110(1):13. PubMed ID: 1731709 [No Abstract] [Full Text] [Related]
14. 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 [TBL] [Abstract][Full Text] [Related]
15. 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; 88(23):10900-4. PubMed ID: 1961759 [TBL] [Abstract][Full Text] [Related]
16. 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; 804():477-90. PubMed ID: 8993566 [No Abstract] [Full Text] [Related]
17. 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; 111(6 Pt 1):2341-51. PubMed ID: 1703535 [TBL] [Abstract][Full Text] [Related]
18. Peroxisomal alanine:glyoxylate aminotransferase and prenatal diagnosis of primary hyperoxaluria type 1. Danpure CJ Lancet; 1986 Nov; 2(8516):1168. PubMed ID: 2877320 [No Abstract] [Full Text] [Related]
19. Human peroxisomal L-alanine: glyoxylate aminotransferase. Evolutionary loss of a mitochondrial targeting signal by point mutation of the initiation codon. Takada Y; Kaneko N; Esumi H; Purdue PE; Danpure CJ Biochem J; 1990 Jun; 268(2):517-20. PubMed ID: 2363689 [TBL] [Abstract][Full Text] [Related]
20. Further studies on the activity and subcellular distribution of alanine:glyoxylate aminotransferase in the livers of patients with primary hyperoxaluria type 1. Danpure CJ; Jennings PR Clin Sci (Lond); 1988 Sep; 75(3):315-22. PubMed ID: 3416563 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]