0000000001188844

AUTHOR

M.-c. Thiard

showing 1 related works from this author

Molecular analysis of a human liver mitochondrial ornithine transcarbamylase deficiency.

1990

The liver of a young girl which had been successfully transplanted was investigated at the ornithine transcarbamylase (OTC, EC 2.1.3.3) gene expression level. Northern blot hybridization using a human OTC cDNA probe showed a greater than 80% decrease in specific OTC mRNA although having the same molecular size as a normal control. OTC polypeptide was simultaneously synthesized with a normal molecular size but at a low level (20%) as shown by immunoblotting. The OTC enzyme from the deficient liver exhibited very little catalytic activity (7.2% as compared to the normal subject). These results may support several explanations of this disease such as mutation of the OTC gene promoter leading t…

Ornithine transcarbamylaseMitochondria LiverBiologymedicine.disease_causeCatalysisOrnithine CarbamoyltransferaseGene expressionGeneticsmedicineHumansNorthern blotRNA MessengerCloning MolecularGenetics (clinical)Ornithine transcarbamylase deficiencyOrnithine CarbamoyltransferaseMutationNucleic Acid HybridizationPromoterDNAmedicine.diseaseBlotting NorthernOrnithine Carbamoyltransferase Deficiency DiseaseBiochemistryUrea cycleChild PreschoolRNAFemalePeptidesJournal of inherited metabolic disease
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