201 related articles for article (PubMed ID: 2717533)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. Aminooxy acetic acid: a selective inhibitor of alanine:glyoxylate aminotransferase and its use in the diagnosis of primary hyperoxaluria type I.
Andy V; Horváth P; Wanders RJ
Clin Chim Acta; 1995 Dec; 243(2):105-14. PubMed ID: 8747487
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Strategies for the prenatal diagnosis of primary hyperoxaluria type 1.
Danpure CJ; Rumsby G
Prenat Diagn; 1996 Jul; 16(7):587-98. PubMed ID: 8843467
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Molecular characterization and clinical use of a polymorphic tandem repeat in an intron of the human alanine:glyoxylate aminotransferase gene.
Danpure CJ; Birdsey GM; Rumsby G; Lumb MJ; Purdue PE; Allsop J
Hum Genet; 1994 Jul; 94(1):55-64. PubMed ID: 8034295
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Enzymological diagnosis of primary hyperoxaluria type 1 by measurement of hepatic alanine: glyoxylate aminotransferase activity.
Danpure CJ; Jennings PR; Watts RW
Lancet; 1987 Feb; 1(8528):289-91. PubMed ID: 2880111
[TBL] [Abstract][Full Text] [Related]
13. Prenatal exclusion of primary hyperoxaluria type 1.
Danpure CJ; Jennings PR; Penketh RJ; Wise PJ; Rodeck CH
Lancet; 1988 Feb; 1(8581):367. PubMed ID: 2893183
[No Abstract] [Full Text] [Related]
14. 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]
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; 123(5):1237-48. PubMed ID: 8245128
[TBL] [Abstract][Full Text] [Related]
16. Micromethod for the assay of glutamate: glyoxylate aminotransferase and modifications of a micromethod for the assay of alanine: glyoxylate aminotransferase. Implications for the prenatal diagnosis of type I hyperoxaluria by fetal liver biopsy.
Toone JR; Applegarth DA
Clin Chim Acta; 1991 Nov; 203(1):105-6. PubMed ID: 1769117
[No Abstract] [Full Text] [Related]
17. 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]
18. Primary hyperoxaluria type I.
Latta K; Brodehl J
Eur J Pediatr; 1990 May; 149(8):518-22. PubMed ID: 2189732
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Exclusion of primary hyperoxaluria type I (PHI) in end-stage renal failure by enzymatic analysis of a percutaneous hepatic biopsy.
Morgan SH; Danpure CJ; Bending MR; Eisinger AJ
Nephron; 1990; 55(3):336-7. PubMed ID: 2370935
[No Abstract] [Full Text] [Related]
[Next] [New Search]