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L Bolund

Showing results (111-120 of 146) with videos related to

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Reproduction (Cambridge, England)|December 27, 2007
High hydrostatic pressure: a new way to improve in vitro developmental competence of porcine matured oocytes after vitrificationY Du, C S Pribenszky, M Molnár, et al.
Acta Haematologica|January 1, 1972
Influence of cell density on the acridine orange binding to deoxyribonucleoprotein complex in leucocytes from patients with infectious mononucleosis and acute leukaemiaL Bolund, L E De Bault, G E Foley, et al.
Biochimica Et Biophysica Acta|October 20, 1993
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 mutationP Bross, B S Andresen, V Winter, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
LDL receptor-GFP fusion proteins: new tools for the characterisation of disease-causing mutations in the LDL receptor geneH U Holst, F Dagnaes-Hansen, T J Corydon, et al.
American Journal of Human Genetics|March 1, 1992
Assignment of the urokinase-type plasminogen activator receptor gene (PLAUR) to chromosome 19q13.1-q13.2A D Børglum, A Byskov, P Ragno, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Molecular genetic characterization and urinary excretion pattern of metabolites in two families with MCAD deficiency due to compound heterozygosity with a 13 base pair insertion in one alleleN Gregersen, V Winter, S Lyonnet, et al.
Human Molecular Genetics|April 1, 1993
A silent A to G mutation in exon 11 of the medium-chain acyl-CoA dehydrogenase (MCAD) geneB S Andresen, S Kølvraa, P Bross, et al.
The Journal of Biological Chemistry|May 28, 1998
Rapid degradation of short-chain acyl-CoA dehydrogenase variants with temperature-sensitive folding defects occurs after import into mitochondriaT J Corydon, P Bross, T G Jensen, et al.
Zeitschrift Fur Gastroenterologie|June 1, 1996
A flow cytometric competition technique for measuring interaction of LDL with cellular LDL-receptors applied to patients with mutant (Arg3500-->Gln) apolipoprotein BF Heath, T G Jensen, P S Hansen, et al.
Human Mutation|January 1, 1995
Comparison between medium-chain acyl-CoA dehydrogenase mutant proteins overexpressed in bacterial and mammalian cellsT G Jensen, P Bross, B S Andresen, et al.
Pageof 15

Showing results (111-120 of 146) with videos related to

Sort By:
Pageof 15
Reproduction (Cambridge, England)|December 27, 2007
High hydrostatic pressure: a new way to improve in vitro developmental competence of porcine matured oocytes after vitrificationY Du, C S Pribenszky, M Molnár, et al.
Acta Haematologica|January 1, 1972
Influence of cell density on the acridine orange binding to deoxyribonucleoprotein complex in leucocytes from patients with infectious mononucleosis and acute leukaemiaL Bolund, L E De Bault, G E Foley, et al.
Biochimica Et Biophysica Acta|October 20, 1993
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 mutationP Bross, B S Andresen, V Winter, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
LDL receptor-GFP fusion proteins: new tools for the characterisation of disease-causing mutations in the LDL receptor geneH U Holst, F Dagnaes-Hansen, T J Corydon, et al.
American Journal of Human Genetics|March 1, 1992
Assignment of the urokinase-type plasminogen activator receptor gene (PLAUR) to chromosome 19q13.1-q13.2A D Børglum, A Byskov, P Ragno, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Molecular genetic characterization and urinary excretion pattern of metabolites in two families with MCAD deficiency due to compound heterozygosity with a 13 base pair insertion in one alleleN Gregersen, V Winter, S Lyonnet, et al.
Human Molecular Genetics|April 1, 1993
A silent A to G mutation in exon 11 of the medium-chain acyl-CoA dehydrogenase (MCAD) geneB S Andresen, S Kølvraa, P Bross, et al.
The Journal of Biological Chemistry|May 28, 1998
Rapid degradation of short-chain acyl-CoA dehydrogenase variants with temperature-sensitive folding defects occurs after import into mitochondriaT J Corydon, P Bross, T G Jensen, et al.
Zeitschrift Fur Gastroenterologie|June 1, 1996
A flow cytometric competition technique for measuring interaction of LDL with cellular LDL-receptors applied to patients with mutant (Arg3500-->Gln) apolipoprotein BF Heath, T G Jensen, P S Hansen, et al.
Human Mutation|January 1, 1995
Comparison between medium-chain acyl-CoA dehydrogenase mutant proteins overexpressed in bacterial and mammalian cellsT G Jensen, P Bross, B S Andresen, et al.
Pageof 15