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Molecular Pharmacology|September 1, 1990
Cysteamine increases homocysteine export and glutathione content by independent mechanisms in C3H/10T1/2 cellsR Djurhuus, A M Svardal, P M UelandTidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|September 30, 1992
[Routine determination of homocysteine in plasma. A new and improved possibility for risk evaluation and diagnosis of common diseases]R J Ulvik, P M Ueland, H RefsumBiochimica Et Biophysica Acta|December 30, 1982
Inhibition of phospholipid methylation in isolated rat hepatocytes by analogues of adenosine and S-adenosylhomocysteineJ S Schanche, T Schanche, P M UelandScandinavian Journal of Clinical and Laboratory Investigation|November 6, 2003
Routine determination of serum methylmalonic acid and plasma total homocysteine in NorwayJ Schneede, P M Ueland, S I KjaerstadJournal of Reproduction and Fertility|August 1, 1975
Protein kinases activated by cAMP in the genital tract of spayed mice treated with oestradiol-17betaS O Doskeland, S Kvinnsland, P M UelandClinical Chemistry|October 7, 1998
Chemical mismatch cleavage combined with capillary electrophoresis: detection of mutations exon 8 of the cystathionine beta-synthase geneJ Ren, A Ulvik, H Refsum, et al.Journal of Cellular Physiology|January 1, 1991
Homocysteine export from cells cultured in the presence of physiological or superfluous levels of methionine: methionine loading of non-transformed, transformed, proliferating, and quiescent cells in cultureB Christensen, H Refsum, O Vintermyr, et al.The American Journal of Clinical Nutrition|March 1, 1994
Redox status and protein binding of plasma homocysteine and other aminothiols in patients with hyperhomocysteinemia due to cobalamin deficiencyM A Mansoor, P M Ueland, A M SvardalAnalytical Biochemistry|December 22, 1999
Applications of short-chain polydimethylacrylamide as sieving medium for the electrophoretic separation of DNA fragments and mutation analysis in uncoated capillariesJ Ren, A Ulvik, H Refsum, et al.The Journal of Pediatrics|March 20, 1998
The C677T mutation in the methylenetetrahydrofolate reductase gene predisposes to hyperhomocysteinemia in children with familial hypercholesterolemia treated with cholestyramineS Tonstad, H Refsum, L Ose, et al.Pageof 45