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Niels Gregersen

Showing results (141-150 of 161) with videos related to

Pageof 17
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Optics Express|May 3, 2018
Benchmarking five numerical simulation techniques for computing resonance wavelengths and quality factors in photonic crystal membrane line defect cavitiesJakob Rosenkrantz de Lasson, Lars Hagedorn Frandsen, Philipp Gutsche, et al.
Stem Cells and Development|October 28, 2016
Mitochondrial Spare Respiratory Capacity Is Negatively Correlated with Nuclear Reprogramming EfficiencyYan Zhou, Rasha Abdelkadhem Al-Saaidi, Paula Fernandez-Guerra, et al.
Human Mutation|October 15, 2013
The ETFDH c.158A>G variation disrupts the balanced interplay of ESE- and ESS-binding proteins thereby causing missplicing and multiple Acyl-CoA dehydrogenation deficiencyRikke K J Olsen, Sabrina Brøner, Rugivan Sabaratnam, et al.
Danish Medical Journal|January 8, 2020
Danish expanded newborn screening is a successful preventive public health programmeAllan Lund, Flemming Wibrand, Kristin Skogstrand, et al.
Gene|May 30, 2002
Genomic organization, transcript variants and comparative analysis of the human nucleoporin 155 (NUP155) geneXiuqing Zhang, Huanming Yang, Jun Yu, et al.
Journal of Inherited Metabolic Disease|September 4, 2010
A comprehensive HADHA c.1528G>C frequency study reveals high prevalence of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency in PolandDorota Piekutowska-Abramczuk, Rikke K J Olsen, Jolanta Wierzba, et al.
Molecular Genetics and Metabolism|January 20, 2007
REMOVED: Short-chain acyl-CoA dehydrogenase gene mutation (319 C>T) presents with clinical heterogeneity and is candidate founder mutation in Ashkenazi Jewish populationIngrid Tein, Orly Elpeleg, Bruria Ben-Zeev, et al.
Molecular Genetics and Metabolism|December 7, 2007
Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish originIngrid Tein, Orly Elpeleg, Bruria Ben-Zeev, et al.
Journal of Human Genetics|October 31, 2006
Single-nucleotide variations in the genes encoding the mitochondrial Hsp60/Hsp10 chaperone system and their disease-causing potentialPeter Bross, Zhijie Li, Jakob Hansen, et al.
Molecular Genetics and Metabolism|May 1, 2012
MCAD deficiency in DenmarkBrage Storstein Andresen, Allan Meldgaard Lund, David Michael Hougaard, et al.
Pageof 17

Showing results (141-150 of 161) with videos related to

Sort By:
Pageof 17
Optics Express|May 3, 2018
Benchmarking five numerical simulation techniques for computing resonance wavelengths and quality factors in photonic crystal membrane line defect cavitiesJakob Rosenkrantz de Lasson, Lars Hagedorn Frandsen, Philipp Gutsche, et al.
Stem Cells and Development|October 28, 2016
Mitochondrial Spare Respiratory Capacity Is Negatively Correlated with Nuclear Reprogramming EfficiencyYan Zhou, Rasha Abdelkadhem Al-Saaidi, Paula Fernandez-Guerra, et al.
Human Mutation|October 15, 2013
The ETFDH c.158A>G variation disrupts the balanced interplay of ESE- and ESS-binding proteins thereby causing missplicing and multiple Acyl-CoA dehydrogenation deficiencyRikke K J Olsen, Sabrina Brøner, Rugivan Sabaratnam, et al.
Danish Medical Journal|January 8, 2020
Danish expanded newborn screening is a successful preventive public health programmeAllan Lund, Flemming Wibrand, Kristin Skogstrand, et al.
Gene|May 30, 2002
Genomic organization, transcript variants and comparative analysis of the human nucleoporin 155 (NUP155) geneXiuqing Zhang, Huanming Yang, Jun Yu, et al.
Journal of Inherited Metabolic Disease|September 4, 2010
A comprehensive HADHA c.1528G>C frequency study reveals high prevalence of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency in PolandDorota Piekutowska-Abramczuk, Rikke K J Olsen, Jolanta Wierzba, et al.
Molecular Genetics and Metabolism|January 20, 2007
REMOVED: Short-chain acyl-CoA dehydrogenase gene mutation (319 C>T) presents with clinical heterogeneity and is candidate founder mutation in Ashkenazi Jewish populationIngrid Tein, Orly Elpeleg, Bruria Ben-Zeev, et al.
Molecular Genetics and Metabolism|December 7, 2007
Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish originIngrid Tein, Orly Elpeleg, Bruria Ben-Zeev, et al.
Journal of Human Genetics|October 31, 2006
Single-nucleotide variations in the genes encoding the mitochondrial Hsp60/Hsp10 chaperone system and their disease-causing potentialPeter Bross, Zhijie Li, Jakob Hansen, et al.
Molecular Genetics and Metabolism|May 1, 2012
MCAD deficiency in DenmarkBrage Storstein Andresen, Allan Meldgaard Lund, David Michael Hougaard, et al.
Pageof 17