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3. 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]
4. 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]
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. 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]
7. 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]
8. Primary hyperoxaluria type 1 and peroxisome-to-mitochondrion mistargeting of alanine:glyoxylate aminotransferase. Danpure CJ Biochimie; 1993; 75(3-4):309-15. PubMed ID: 8507692 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Molecular and clinical heterogeneity in primary hyperoxaluria type 1. Danpure CJ Am J Kidney Dis; 1991 Apr; 17(4):366-9. PubMed ID: 2008900 [TBL] [Abstract][Full Text] [Related]
12. Primary hyperoxaluria type I. Watts RW QJM; 1994 Oct; 87(10):593-600. PubMed ID: 7987654 [No Abstract] [Full Text] [Related]
13. 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; 135(4):939-51. PubMed ID: 8922378 [TBL] [Abstract][Full Text] [Related]
15. Rapid identification of primary hyperoxaluria type I patients using a novel, fully automated method for measurement of hepatic alanine: glyoxylate aminotransferase. Horváth VA; Wanders RJ J Inherit Metab Dis; 1994; 17(3):336-8. PubMed ID: 7807946 [No Abstract] [Full Text] [Related]
16. [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]
17. 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]
18. 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]
19. Enzymatic prenatal diagnosis of primary hyperoxaluria type 1: potential and limitations. Danpure CJ; Cooper PJ; Jennings PR; Wise PJ; Penketh RJ; Rodeck CH J Inherit Metab Dis; 1989; 12 Suppl 2():286-8. PubMed ID: 2512427 [No Abstract] [Full Text] [Related]
20. [Adult type I primary hyperoxaluria: 2 cases confirmed by liver biopsy at end-stage renal insufficiency]. Schillinger F; Mahmoud M; Montagnac R; Collin P; Milcent T Nephrologie; 1990; 11(4):217-21. PubMed ID: 2074921 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]