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Showing results (201-210 of 227) with videos related to

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APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|July 14, 2011
Sequence analysis of HIV-1 isolates from Guinea-Bissau: selection of vaccine epitopes relevant in both West African and European countriesLasse Vinner, Birgitta Holmgren, Kristoffer J Jensen, et al.
Journal of Inherited Metabolic Disease|November 25, 2010
Urgent metabolic service improves survival in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screeningJolanta Sykut-Cegielska, Wanda Gradowska, Dorota Piekutowska-Abramczuk, et al.
Nature|December 6, 2016
Splicing factor 1 modulates dietary restriction and TORC1 pathway longevity in C. elegansCaroline Heintz, Thomas Koed Doktor, Anne Lanjuin, et al.
Pediatric Research|June 1, 1996
Ethylmalonic aciduria is associated with an amino acid variant of short chain acyl-coenzyme A dehydrogenaseM J Corydon, N Gregersen, W Lehnert, et al.
Nature|July 13, 2017
Corrigendum: Splicing factor 1 modulates dietary restriction and TORC1 pathway longevity in C. elegansCaroline Heintz, Thomas K Doktor, Anne Lanjuin, et al.
Atherosclerosis|May 1, 1997
A common W556S mutation in the LDL receptor gene of Danish patients with familial hypercholesterolemia encodes a transport-defective proteinH K Jensen, H Holst, L G Jensen, et al.
Acta Physiologica (Oxford, England)|January 11, 2026
Acyl-CoA Binding Protein in White and Brown Adipose Tissue Is Dispensable for Systemic Energy Metabolism in MiceM F Nørremark, R Petersen, P M M Ruppert, et al.
Cancer Cell International|December 26, 2024
Protein kinase CK2 sustains de novo fatty acid synthesis by regulating the expression of SCD-1 in human renal cancer cellsBarbara Guerra, Kristina Jurcic, Rachelle van der Poel, et al.
Journal of Inherited Metabolic Disease|November 8, 2003
Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiencyS E Olpin, A Afifi, S Clark, et al.
Neuromuscular Disorders : NMD|March 31, 2009
Diagnostic assessment and long-term follow-up of 13 patients with Very Long-Chain Acyl-Coenzyme A dehydrogenase (VLCAD) deficiencyPascal Laforêt, Cécile Acquaviva-Bourdain, Odile Rigal, et al.
Pageof 23

Showing results (201-210 of 227) with videos related to

Sort By:
Pageof 23
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|July 14, 2011
Sequence analysis of HIV-1 isolates from Guinea-Bissau: selection of vaccine epitopes relevant in both West African and European countriesLasse Vinner, Birgitta Holmgren, Kristoffer J Jensen, et al.
Journal of Inherited Metabolic Disease|November 25, 2010
Urgent metabolic service improves survival in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screeningJolanta Sykut-Cegielska, Wanda Gradowska, Dorota Piekutowska-Abramczuk, et al.
Nature|December 6, 2016
Splicing factor 1 modulates dietary restriction and TORC1 pathway longevity in C. elegansCaroline Heintz, Thomas Koed Doktor, Anne Lanjuin, et al.
Pediatric Research|June 1, 1996
Ethylmalonic aciduria is associated with an amino acid variant of short chain acyl-coenzyme A dehydrogenaseM J Corydon, N Gregersen, W Lehnert, et al.
Nature|July 13, 2017
Corrigendum: Splicing factor 1 modulates dietary restriction and TORC1 pathway longevity in C. elegansCaroline Heintz, Thomas K Doktor, Anne Lanjuin, et al.
Atherosclerosis|May 1, 1997
A common W556S mutation in the LDL receptor gene of Danish patients with familial hypercholesterolemia encodes a transport-defective proteinH K Jensen, H Holst, L G Jensen, et al.
Acta Physiologica (Oxford, England)|January 11, 2026
Acyl-CoA Binding Protein in White and Brown Adipose Tissue Is Dispensable for Systemic Energy Metabolism in MiceM F Nørremark, R Petersen, P M M Ruppert, et al.
Cancer Cell International|December 26, 2024
Protein kinase CK2 sustains de novo fatty acid synthesis by regulating the expression of SCD-1 in human renal cancer cellsBarbara Guerra, Kristina Jurcic, Rachelle van der Poel, et al.
Journal of Inherited Metabolic Disease|November 8, 2003
Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiencyS E Olpin, A Afifi, S Clark, et al.
Neuromuscular Disorders : NMD|March 31, 2009
Diagnostic assessment and long-term follow-up of 13 patients with Very Long-Chain Acyl-Coenzyme A dehydrogenase (VLCAD) deficiencyPascal Laforêt, Cécile Acquaviva-Bourdain, Odile Rigal, et al.
Pageof 23