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Characterization of wild-type human medium-chain acyl-CoA dehydrogenase (MCAD) and mutant enzymes present in MCAD-deficient patients by two-dimensional gel electrophoresis: evidence for post-translational modification of the enzyme.
Bross P, Jensen TG, Andresen BS, Kjeldsen M, Nandy A, Kølvraa S, Ghisla S, Rasched I, Bolund L, Gregersen N. Bross P, et al. Among authors: ghisla s. Biochem Med Metab Biol. 1994 Jun;52(1):36-44. doi: 10.1006/bmmb.1994.1031. Biochem Med Metab Biol. 1994. PMID: 7917465
Co-overexpression of bacterial GroESL chaperonins partly overcomes non-productive folding and tetramer assembly of E. coli-expressed human medium-chain acyl-CoA dehydrogenase (MCAD) carrying the prevalent disease-causing K304E mutation.
Bross P, Andresen BS, Winter V, Kräutle F, Jensen TG, Nandy A, Kølvraa S, Ghisla S, Bolund L, Gregersen N. Bross P, et al. Among authors: ghisla s. Biochim Biophys Acta. 1993 Oct 20;1182(3):264-74. doi: 10.1016/0925-4439(93)90068-c. Biochim Biophys Acta. 1993. PMID: 8104486
Biochemical characterization of purified, human recombinant Lys304-->Glu medium-chain acyl-CoA dehydrogenase containing the common disease-causing mutation and comparison with the normal enzyme.
Kieweg V, Kräutle FG, Nandy A, Engst S, Vock P, Abdel-Ghany AG, Bross P, Gregersen N, Rasched I, Strauss A, Ghisla S. Kieweg V, et al. Among authors: ghisla s. Eur J Biochem. 1997 Jun 1;246(2):548-56. doi: 10.1111/j.1432-1033.1997.00548.x. Eur J Biochem. 1997. PMID: 9208949 Free article.
166 results