Ornithine carbamoyltransferase (OCT) in the jejunal mucosa, as a reference of the liver OCT
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference20 articles.
1. Hyperammonia due to a mutant enzyme of omithine transcarbamylase;Matsuda;Pediatrics,1971
2. Metabolic and genetic studies of a family with omithine transcarbamylase deficiency;Goldstein;Pediatr Res,1974
3. Some kinetic properties of liver omithine carbamoyl transferase (OCT) in a patient with OCT deficiency;Van der Heiden;Clin Chim Acta,1977
4. Leukocyte urea cycle enzymes in hypeorammonemia;Wolfe;Pediatr Res,1975
5. Heterogenous mutations of the structural gene of human omithine carbamoyltransferase as observed in five personal cases;Cathelineau;Enzyme,1974
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3. Correction of Ornithine Transcarbamylase Deficiency in AdultspfashMice and in OTC-Deficient Human Hepatocytes with Recombinant Adenoviruses Bearing the CAG Promoter;Human Gene Therapy;1996-05
4. Compared expression levels of ornithine transcarbamylase and carbamylphosphate synthetase in liver and small intestine of normal and mutant mice;Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression;1988-09
5. Attempts to Investigate the Molecular Basis of Urea Cycle Disorders;Pediatrics International;1987-08
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