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The hyperornithinemia–hyperammonemia–homocitrullinuria syndrome is a rare autosomal recessive disorder caused by the functional… Expand PURPOSE
A prior report showed ornithine cytotoxicity in ornithine-delta-aminotransferase (OAT)-deficient human retinal pigment… Expand SummaryWith the technique of stop flow microperfusion with simultaneous capillary microperfusion the zero net flux transtubular… Expand The purpose of this study was to find whether the concentration of N-acetylglutamate and ornithine transport into mitochondria… Expand Male mice carrying the spfash mutation have 5-10% of the normal activity of ornithine carbamoyltransferase, yet are only slightly… Expand Streptococcus lactis metabolizes arginine by the arginine deiminase (ADI) pathway. Resting cells of S. lactis grown in the… Expand In the presence of citrulline synthesis, we made the following observations. External ornithine is channeled between its… Expand The map location of two genes, abpR and abpS, was established. The abpR locus is responsible for the synthesis and the abpS locus… Expand 1. The characteristics of ornithine catabolism by the aminotransferase pathway in isolated mitochondria were determined. 2… Expand A mutant of Escherichia coli strain CanR 22 has been isolated which is resistant to growth inhibition by canavanine, an analogue… Expand