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N Gregersen

Showing results (101-110 of 208) with videos related to

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Progress in Clinical and Biological Research|January 1, 1992
Medium chain acyl-CoA dehydrogenase deficiency in the United KingdomD Curtis, A I Blakemore, P C Engel, et al.
Journal of Inherited Metabolic Disease|June 19, 2001
The role of chaperone-assisted folding and quality control in inborn errors of metabolism: protein folding disordersN Gregersen, P Bross, B S Andrese, et al.
Clinical Genetics|April 1, 1996
A G-1-to-A acceptor splice site LDLR mutant allele leads to reduced relative transcript levels in patients with heterozygous familial hypercholesterolemiaH K Jensen, L G Jensen, P S Hansen, et al.
Clinical Genetics|February 1, 1994
Apolipoprotein B gene polymorphisms in ischemic heart disease and hypercholesterolemia: effects of age and sexP S Hansen, I C Klausen, L Lemming, et al.
Atherosclerosis|October 26, 1999
Spectrum of LDL receptor gene mutations in Denmark: implications for molecular diagnostic strategy in heterozygous familial hypercholesterolemiaH K Jensen, L G Jensen, H Meinertz, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 15, 1983
General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three casesN Gregersen, S Kølvraa, K Rasmussen, et al.
Clinical Genetics|June 1, 1991
DNA deletions in the low density lipoprotein (LDL) receptor gene in Danish families with familial hypercholesterolemiaN S Rüdiger, E M Heinsvig, F A Hansen, et al.
Archives of Orthopaedic and Trauma Surgery|January 1, 1990
Antibiotic prophylaxis in lower-extremity amputations due to ischemia. A prospective, randomized trial of cephalothin versus methicillinS Thomsen, B W Jakobsen, J O Wethelund, et al.
The Biochemical Journal|May 16, 1998
A human homologue of Escherichia coli ClpP caseinolytic protease: recombinant expression, intracellular processing and subcellular localizationT J Corydon, P Bross, H U Holst, et al.
American Journal of Human Genetics|January 1, 1996
Identification of 13 new mutations in the vasopressin-neurophysin II gene in 17 kindreds with familial autosomal dominant neurohypophyseal diabetes insipidusS Rittig, G L Robertson, C Siggaard, et al.
Pageof 21

Showing results (101-110 of 208) with videos related to

Sort By:
Pageof 21
Progress in Clinical and Biological Research|January 1, 1992
Medium chain acyl-CoA dehydrogenase deficiency in the United KingdomD Curtis, A I Blakemore, P C Engel, et al.
Journal of Inherited Metabolic Disease|June 19, 2001
The role of chaperone-assisted folding and quality control in inborn errors of metabolism: protein folding disordersN Gregersen, P Bross, B S Andrese, et al.
Clinical Genetics|April 1, 1996
A G-1-to-A acceptor splice site LDLR mutant allele leads to reduced relative transcript levels in patients with heterozygous familial hypercholesterolemiaH K Jensen, L G Jensen, P S Hansen, et al.
Clinical Genetics|February 1, 1994
Apolipoprotein B gene polymorphisms in ischemic heart disease and hypercholesterolemia: effects of age and sexP S Hansen, I C Klausen, L Lemming, et al.
Atherosclerosis|October 26, 1999
Spectrum of LDL receptor gene mutations in Denmark: implications for molecular diagnostic strategy in heterozygous familial hypercholesterolemiaH K Jensen, L G Jensen, H Meinertz, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 15, 1983
General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three casesN Gregersen, S Kølvraa, K Rasmussen, et al.
Clinical Genetics|June 1, 1991
DNA deletions in the low density lipoprotein (LDL) receptor gene in Danish families with familial hypercholesterolemiaN S Rüdiger, E M Heinsvig, F A Hansen, et al.
Archives of Orthopaedic and Trauma Surgery|January 1, 1990
Antibiotic prophylaxis in lower-extremity amputations due to ischemia. A prospective, randomized trial of cephalothin versus methicillinS Thomsen, B W Jakobsen, J O Wethelund, et al.
The Biochemical Journal|May 16, 1998
A human homologue of Escherichia coli ClpP caseinolytic protease: recombinant expression, intracellular processing and subcellular localizationT J Corydon, P Bross, H U Holst, et al.
American Journal of Human Genetics|January 1, 1996
Identification of 13 new mutations in the vasopressin-neurophysin II gene in 17 kindreds with familial autosomal dominant neurohypophyseal diabetes insipidusS Rittig, G L Robertson, C Siggaard, et al.
Pageof 21