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S Andresen

Showing results (121-130 of 227) with videos related to

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Thrombosis Research|July 1, 2004
The ability of three global plasma assays to recognize thrombophiliaMarianne S Andresen, Ulrich Abildgaard, Sigurd Liestøl, 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.
The Journal of Biological Chemistry|March 30, 2001
Tumor suppressor p53 protein is a new target for the metastasis-associated Mts1/S100A4 protein: functional consequences of their interactionM Grigorian, S Andresen, E Tulchinsky, et al.
JIMD Reports|March 13, 2015
Abnormal Newborn Screening in a Healthy Infant of a Mother with Undiagnosed Medium-Chain Acyl-CoA Dehydrogenase DeficiencyLise Aksglaede, Mette Christensen, Jess H Olesen, et al.
The Journal of Biological Chemistry|April 28, 1995
Effects of two mutations detected in medium chain acyl-CoA dehydrogenase (MCAD)-deficient patients on folding, oligomer assembly, and stability of MCAD enzymeP Bross, C Jespersen, T G Jensen, et al.
Prenatal Diagnosis|January 1, 1995
Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in a family with a previous fatal case of sudden unexpected death in childhoodN Gregersen, V Winter, P K Jensen, et al.
Annals of Neurology|April 18, 1998
Very long chain acyl-coenzyme A dehydrogenase deficiency with adult onsetA H Smelt, B J Poorthuis, W Onkenhout, et al.
Journal of Inherited Metabolic Disease|January 27, 2005
Lipid-storage myopathy and respiratory insufficiency due to ETFQO mutations in a patient with late-onset multiple acyl-CoA dehydrogenation deficiencyR K J Olsen, M Pourfarzam, A A M Morris, 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.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|October 9, 2025
Risk Factors and Preceding Events Predisposing the Development of Superior Canal Dehiscence SyndromeOren Wei, Pavan S Krishnan, Eric J Formeister, et al.
Pageof 23

Showing results (121-130 of 227) with videos related to

Sort By:
Pageof 23
Thrombosis Research|July 1, 2004
The ability of three global plasma assays to recognize thrombophiliaMarianne S Andresen, Ulrich Abildgaard, Sigurd Liestøl, 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.
The Journal of Biological Chemistry|March 30, 2001
Tumor suppressor p53 protein is a new target for the metastasis-associated Mts1/S100A4 protein: functional consequences of their interactionM Grigorian, S Andresen, E Tulchinsky, et al.
JIMD Reports|March 13, 2015
Abnormal Newborn Screening in a Healthy Infant of a Mother with Undiagnosed Medium-Chain Acyl-CoA Dehydrogenase DeficiencyLise Aksglaede, Mette Christensen, Jess H Olesen, et al.
The Journal of Biological Chemistry|April 28, 1995
Effects of two mutations detected in medium chain acyl-CoA dehydrogenase (MCAD)-deficient patients on folding, oligomer assembly, and stability of MCAD enzymeP Bross, C Jespersen, T G Jensen, et al.
Prenatal Diagnosis|January 1, 1995
Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in a family with a previous fatal case of sudden unexpected death in childhoodN Gregersen, V Winter, P K Jensen, et al.
Annals of Neurology|April 18, 1998
Very long chain acyl-coenzyme A dehydrogenase deficiency with adult onsetA H Smelt, B J Poorthuis, W Onkenhout, et al.
Journal of Inherited Metabolic Disease|January 27, 2005
Lipid-storage myopathy and respiratory insufficiency due to ETFQO mutations in a patient with late-onset multiple acyl-CoA dehydrogenation deficiencyR K J Olsen, M Pourfarzam, A A M Morris, 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.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|October 9, 2025
Risk Factors and Preceding Events Predisposing the Development of Superior Canal Dehiscence SyndromeOren Wei, Pavan S Krishnan, Eric J Formeister, et al.
Pageof 23