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2. On the biologic origin of C6-C10-dicarboxylic and C6-C10-omega-1-hydroxy monocarboxylic acids in human and rat with acyl-CoA dehydrogenation deficiencies: in vitro studies on the omega- and omega-1-oxidation of medium-chain (C6-C12) fatty acids in human and rat liver. Gregersen N; Mortensen PB; Kølvraa S Pediatr Res; 1983 Oct; 17(10):828-34. PubMed ID: 6634246 [TBL] [Abstract][Full Text] [Related]
3. Formation and degradation of dicarboxylic acids in relation to alterations in fatty acid oxidation in rats. Mortensen PB Biochim Biophys Acta; 1992 Feb; 1124(1):71-9. PubMed ID: 1543729 [TBL] [Abstract][Full Text] [Related]
4. General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases. Gregersen N; Kølvraa S; Rasmussen K; Mortensen PB; Divry P; David M; Hobolth N Clin Chim Acta; 1983 Aug; 132(2):181-91. PubMed ID: 6616873 [TBL] [Abstract][Full Text] [Related]
5. 3-hydroxydecanedioic acid and related homologues: urinary metabolites in ketoacidosis. Greter J; Lindstedt S; Seeman H; Steen G Clin Chem; 1980 Feb; 26(2):261-5. PubMed ID: 7353273 [TBL] [Abstract][Full Text] [Related]
6. The biological origin of ketotic dicarboxylic aciduria. In vivo and in vitro investigations of the omega-oxidation of C6-C16-monocarboxylic acids in unstarved, starved and diabetic rats. Mortensen PB; Gregersen N Biochim Biophys Acta; 1981 Dec; 666(3):394-404. PubMed ID: 6798996 [TBL] [Abstract][Full Text] [Related]
7. Biogenesis of dicarboxylic acids in rat liver homogenate studied by 13C labeling. Jin SJ; Tserng KY Am J Physiol; 1991 Dec; 261(6 Pt 1):E719-24. PubMed ID: 1767832 [TBL] [Abstract][Full Text] [Related]
8. In vitro studies on the oxidation of medium-chain dicarboxylic acids in rat liver. Kølvraa S; Gregersen N Biochim Biophys Acta; 1986 May; 876(3):515-25. PubMed ID: 3707982 [TBL] [Abstract][Full Text] [Related]
9. (omega-1)-Hydroxymonocarboxylic acids in urine of infants fed medium-chain triglycerides. Shigematsu Y; Momoi T; Sudo M; Suzuki Y Clin Chem; 1981 Oct; 27(10):1661-4. PubMed ID: 7285316 [TBL] [Abstract][Full Text] [Related]
10. C6-C10-dicarboxylic aciduria: biochemical considerations in relation to diagnosis of beta-oxidation defects. Gregersen N; Kølvraa S; Mortensen PB; Rasmussen K Scand J Clin Lab Invest Suppl; 1982; 161():15-27. PubMed ID: 6959231 [TBL] [Abstract][Full Text] [Related]
11. The biological origin of ketotic dicarboxylic aciduria. II. In vivo and in vitro investigations of the beta-oxidation of C8-C16-dicarboxylic acids in unstarved, starved and diabetic rats. Mortensen PB; Gregersen N Biochim Biophys Acta; 1982 Mar; 710(3):477-84. PubMed ID: 7074126 [TBL] [Abstract][Full Text] [Related]
12. The influence of intravenous medium- and long-chain triglycerides and carnitine on the excretion of dicarboxylic acids. Böhles H; Akçetin Z; Lehnert W JPEN J Parenter Enteral Nutr; 1987; 11(1):46-8. PubMed ID: 3102781 [TBL] [Abstract][Full Text] [Related]
13. Interactions between the omega- and beta-oxidations of fatty acids. Vamecq J; Draye JP J Biochem; 1987 Jul; 102(1):225-34. PubMed ID: 3667564 [TBL] [Abstract][Full Text] [Related]
14. Urinary 3-hydroxydicarboxylic acids in pathophysiology of metabolic disorders with dicarboxylic aciduria. Tserng KY; Jin SJ; Kerr DS; Hoppel CL Metabolism; 1991 Jul; 40(7):676-82. PubMed ID: 1870421 [TBL] [Abstract][Full Text] [Related]
15. Omega-oxidation of fatty acids studied in isolated liver cells. Christensen E; Grønn M; Hagve TA; Christophersen BO Biochim Biophys Acta; 1991 Jan; 1081(2):167-73. PubMed ID: 1998734 [TBL] [Abstract][Full Text] [Related]
16. Identification of isomeric unsaturated medium-chain dicarboxylic acids in human urine. Jin SJ; Tserng KY J Lipid Res; 1989 Oct; 30(10):1611-9. PubMed ID: 2614263 [TBL] [Abstract][Full Text] [Related]
17. The excretion of C6-C10-dicarboxylic acids in the urine of newborn infants during starvation. Evidence for omega-oxidation of fatty acids in the newborn. Gregersen N; Ingerslev J Acta Paediatr Scand; 1979 Sep; 68(5):677-81. PubMed ID: 525335 [TBL] [Abstract][Full Text] [Related]
18. Urinary excretion of dicarboxylic acids from patients with the Zellweger syndrome. Importance of peroxisomes in beta-oxidation of dicarboxylic acids. Björkhem I; Blomstrand S; Hågå P; Kase BF; Palonek E; Pedersen JI; Strandvik B; Wikström SA Biochim Biophys Acta; 1984 Aug; 795(1):15-9. PubMed ID: 6466694 [TBL] [Abstract][Full Text] [Related]
19. Metabolic origins of urinary unsaturated dicarboxylic acids. Jin SJ; Tserng KY Biochemistry; 1990 Sep; 29(37):8540-7. PubMed ID: 2271537 [TBL] [Abstract][Full Text] [Related]
20. Distinction of dicarboxylic aciduria due to medium-chain triglyceride feeding from that due to abnormal fatty acid oxidation and fasting in children. Tserng KY; Griffin RL; Kerr DS Metabolism; 1996 Feb; 45(2):162-7. PubMed ID: 8596483 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]