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N Gregersen

Showing results (151-160 of 208) with videos related to

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Clinical Genetics|August 1, 1994
An alanine29-serine variant in exon 2 of the low density lipoprotein receptor gene: no association with hypercholesterolemiaH K Jensen, L G Jensen, P S Hansen, et al.
Blood|July 1, 1997
Sequence analysis of the Epstein-Barr virus (EBV) latent membrane protein-1 gene and promoter region: identification of four variants among wild-type EBV isolatesK Sandvej, J W Gratama, M Munch, et al.
Clinical Chemistry|November 1, 1995
Improved RNase protection assay for quantifying LDL-receptor mRNA; estimation of analytical imprecision and biological variance in peripheral blood mononuclear cellsN E Petersen, L K Larsen, H Nissen, et al.
Clinical Genetics|November 1, 1996
Phenotypic characterization of a patient homozygous for the D558N LDL receptor gene mutationH K Jensen, L G Jensen, F Heath, et al.
Neuroscience|April 2, 2008
Decreased expression of the mitochondrial matrix proteases Lon and ClpP in cells from a patient with hereditary spastic paraplegia (SPG13)J Hansen, T J Corydon, J Palmfeldt, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 26, 2000
Human and mouse mitochondrial orthologs of bacterial ClpXT J Corydon, M Wilsbech, C Jespersgaard, et al.
Ugeskrift for Laeger|April 15, 2000
[Keratin diseases]P K Jensen, C B Sørensen, B S Andresen, et al.
The Journal of Biological Chemistry|July 25, 2000
Grp78 is involved in retention of mutant low density lipoprotein receptor protein in the endoplasmic reticulumM M Jørgensen, O N Jensen, H U Holst, et al.
Clinical Genetics|July 18, 2002
LDL receptor mutation genotype and vascular disease phenotype in heterozygous familial hypercholesterolaemiaJ U Brorholt-Petersen, H K Jensen, J M Jensen, et al.
Human Genetics|April 1, 1991
Molecular characterization of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: identification of a lys329 to glu mutation in the MCAD gene, and expression of inactive mutant enzyme protein in E. coliN Gregersen, B S Andresen, P Bross, et al.
Pageof 21

Showing results (151-160 of 208) with videos related to

Sort By:
Pageof 21
Clinical Genetics|August 1, 1994
An alanine29-serine variant in exon 2 of the low density lipoprotein receptor gene: no association with hypercholesterolemiaH K Jensen, L G Jensen, P S Hansen, et al.
Blood|July 1, 1997
Sequence analysis of the Epstein-Barr virus (EBV) latent membrane protein-1 gene and promoter region: identification of four variants among wild-type EBV isolatesK Sandvej, J W Gratama, M Munch, et al.
Clinical Chemistry|November 1, 1995
Improved RNase protection assay for quantifying LDL-receptor mRNA; estimation of analytical imprecision and biological variance in peripheral blood mononuclear cellsN E Petersen, L K Larsen, H Nissen, et al.
Clinical Genetics|November 1, 1996
Phenotypic characterization of a patient homozygous for the D558N LDL receptor gene mutationH K Jensen, L G Jensen, F Heath, et al.
Neuroscience|April 2, 2008
Decreased expression of the mitochondrial matrix proteases Lon and ClpP in cells from a patient with hereditary spastic paraplegia (SPG13)J Hansen, T J Corydon, J Palmfeldt, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 26, 2000
Human and mouse mitochondrial orthologs of bacterial ClpXT J Corydon, M Wilsbech, C Jespersgaard, et al.
Ugeskrift for Laeger|April 15, 2000
[Keratin diseases]P K Jensen, C B Sørensen, B S Andresen, et al.
The Journal of Biological Chemistry|July 25, 2000
Grp78 is involved in retention of mutant low density lipoprotein receptor protein in the endoplasmic reticulumM M Jørgensen, O N Jensen, H U Holst, et al.
Clinical Genetics|July 18, 2002
LDL receptor mutation genotype and vascular disease phenotype in heterozygous familial hypercholesterolaemiaJ U Brorholt-Petersen, H K Jensen, J M Jensen, et al.
Human Genetics|April 1, 1991
Molecular characterization of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: identification of a lys329 to glu mutation in the MCAD gene, and expression of inactive mutant enzyme protein in E. coliN Gregersen, B S Andresen, P Bross, et al.
Pageof 21