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Journal of Inherited Metabolic Disease|January 1, 1987
Primary hyperoxaluria type I: ultrastructural observations in liver biopsiesT C Iancu, C J DanpureTrends in Cell Biology|June 1, 1995
How can the products of a single gene be localized to more than one intracellular compartment?C J DanpureBioessays : News and Reviews in Molecular, Cellular and Developmental Biology|April 1, 1997
Variable peroxisomal and mitochondrial targeting of alanine: glyoxylate aminotransferase in mammalian evolution and diseaseC J DanpureThe Biochemical Journal|December 15, 1981
The effect of chloroquine on the metabolism of [35S]cystine in normal and cystinotic human skin fibroblastsC J DanpureBiochimie|January 1, 1993
Primary hyperoxaluria type 1 and peroxisome-to-mitochondrion mistargeting of alanine:glyoxylate aminotransferaseC J DanpureNephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1995
Advances in the enzymology and molecular genetics of primary hyperoxaluria type 1. Prospects for gene therapyC J DanpureJournal of Nephrology|May 30, 1998
The molecular basis of alanine: glyoxylate aminotransferase mistargeting: the most common single cause of primary hyperoxaluria type 1C J DanpureAmerican Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 1, 1991
Molecular and clinical heterogeneity in primary hyperoxaluria type 1C J DanpureUltrastructural Pathology|January 1, 1992
The ultrastructural spectrum of lysosomal storage diseasesT C IancuPageof 12