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N Gregersen

Showing results (171-180 of 208) with videos related to

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Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|February 1, 1994
Characteristics of 46 heterozygous carriers and 57 unaffected relatives in five Danish families with familial defective apolipoprotein B-100P S Hansen, H Meinertz, H K Jensen, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1990
Molecular characterization of inherited medium-chain acyl-CoA dehydrogenase deficiencyD P Kelly, A J Whelan, M L Ogden, 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.
Human Mutation|January 1, 1992
Mutations in the medium chain acyl-CoA dehydrogenase (MCAD) geneK Tanaka, I Yokota, P M Coates, 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.
Human Genetics|August 1, 1991
The most common mutation causing medium-chain acyl-CoA dehydrogenase deficiency is strongly associated with a particular haplotype in the region of the geneS Kølvraa, N Gregersen, A I Blakemore, 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.
The Journal of Clinical Investigation|May 20, 1999
Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathyJ Mogensen, I C Klausen, A K Pedersen, et al.
European Journal of Biochemistry|June 1, 1997
Biochemical characterization of purified, human recombinant Lys304-->Glu medium-chain acyl-CoA dehydrogenase containing the common disease-causing mutation and comparison with the normal enzymeV Kieweg, F G Kräutle, A Nandy, et al.
Clinical Genetics|July 1, 1995
Complexity of molecular genetics of dyslipidemia in a family highly susceptible to ischemic heart diseaseH K Jensen, P S Hansen, L G Jensen, et al.
Pageof 21

Showing results (171-180 of 208) with videos related to

Sort By:
Pageof 21
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|February 1, 1994
Characteristics of 46 heterozygous carriers and 57 unaffected relatives in five Danish families with familial defective apolipoprotein B-100P S Hansen, H Meinertz, H K Jensen, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1990
Molecular characterization of inherited medium-chain acyl-CoA dehydrogenase deficiencyD P Kelly, A J Whelan, M L Ogden, 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.
Human Mutation|January 1, 1992
Mutations in the medium chain acyl-CoA dehydrogenase (MCAD) geneK Tanaka, I Yokota, P M Coates, 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.
Human Genetics|August 1, 1991
The most common mutation causing medium-chain acyl-CoA dehydrogenase deficiency is strongly associated with a particular haplotype in the region of the geneS Kølvraa, N Gregersen, A I Blakemore, 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.
The Journal of Clinical Investigation|May 20, 1999
Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathyJ Mogensen, I C Klausen, A K Pedersen, et al.
European Journal of Biochemistry|June 1, 1997
Biochemical characterization of purified, human recombinant Lys304-->Glu medium-chain acyl-CoA dehydrogenase containing the common disease-causing mutation and comparison with the normal enzymeV Kieweg, F G Kräutle, A Nandy, et al.
Clinical Genetics|July 1, 1995
Complexity of molecular genetics of dyslipidemia in a family highly susceptible to ischemic heart diseaseH K Jensen, P S Hansen, L G Jensen, et al.
Pageof 21