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Joél Smet

Showing results (1-10 of 47) with videos related to

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Medical Hypotheses|July 30, 2020
A capital role for the brain's insula in the diverse fibromyalgia-associated symptomsBoel De Paepe, Joél Smet, Chris Baeken, et al.
Electrophoresis|September 5, 2002
Mass spectrometric identification of mitochondrial oxidative phosphorylation subunits separated by two-dimensional blue-native polyacrylamide gel electrophoresisBart Devreese, Frank Vanrobaeys, Joél Smet, et al.
Acta Neurologica Belgica|December 13, 2007
The aerobic forearm exercise test, a non-invasive tool to screen for mitochondrial disordersAnn Meulemans, Erik Gerlo, Sara Seneca, et al.
Radiation Research|March 8, 2013
Unraveling the mechanisms behind the enhanced MTT conversion by irradiated breast cancer cellsStéphanie Blockhuys, Barbara Vanhoecke, Joél Smet, et al.
European Journal of Pediatrics|July 11, 2014
Extremely high mutation load of the mitochondrial 8993 T>G mutation in a newborn: implications for prognosis and family planning decisionsClaudine De Praeter, Arnaud Vanlander, Piet Vanhaesebrouck, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 16, 2004
Analysis of the mitochondrial encoded subunits of complex I in 20 patients with a complex I deficiencyAnn Meulemans, Willy Lissens, Rudy Van Coster, et al.
Journal of Inherited Metabolic Disease|January 19, 2010
Aberrant synthesis of ATP synthase resulting from a novel deletion in mitochondrial DNA in an African patient with progressive external ophthalmoplegiaFrancois H van der Westhuizen, Joél Smet, Oksana Levanets, et al.
Journal of Inherited Metabolic Disease|April 13, 2011
Complex III staining in blue native polyacrylamide gelsJoél Smet, Boel De Paepe, Sara Seneca, et al.
Archives of Neurology|September 12, 2007
Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathyAnn Meulemans, Boel De Paepe, Jan De Bleecker, et al.
Archives of Neurology|August 16, 2006
A novel mitochondrial transfer RNA(Asn) mutation causing multiorgan failureAnn Meulemans, Sara Seneca, Lieven Lagae, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Medical Hypotheses|July 30, 2020
A capital role for the brain's insula in the diverse fibromyalgia-associated symptomsBoel De Paepe, Joél Smet, Chris Baeken, et al.
Electrophoresis|September 5, 2002
Mass spectrometric identification of mitochondrial oxidative phosphorylation subunits separated by two-dimensional blue-native polyacrylamide gel electrophoresisBart Devreese, Frank Vanrobaeys, Joél Smet, et al.
Acta Neurologica Belgica|December 13, 2007
The aerobic forearm exercise test, a non-invasive tool to screen for mitochondrial disordersAnn Meulemans, Erik Gerlo, Sara Seneca, et al.
Radiation Research|March 8, 2013
Unraveling the mechanisms behind the enhanced MTT conversion by irradiated breast cancer cellsStéphanie Blockhuys, Barbara Vanhoecke, Joél Smet, et al.
European Journal of Pediatrics|July 11, 2014
Extremely high mutation load of the mitochondrial 8993 T>G mutation in a newborn: implications for prognosis and family planning decisionsClaudine De Praeter, Arnaud Vanlander, Piet Vanhaesebrouck, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 16, 2004
Analysis of the mitochondrial encoded subunits of complex I in 20 patients with a complex I deficiencyAnn Meulemans, Willy Lissens, Rudy Van Coster, et al.
Journal of Inherited Metabolic Disease|January 19, 2010
Aberrant synthesis of ATP synthase resulting from a novel deletion in mitochondrial DNA in an African patient with progressive external ophthalmoplegiaFrancois H van der Westhuizen, Joél Smet, Oksana Levanets, et al.
Journal of Inherited Metabolic Disease|April 13, 2011
Complex III staining in blue native polyacrylamide gelsJoél Smet, Boel De Paepe, Sara Seneca, et al.
Archives of Neurology|September 12, 2007
Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathyAnn Meulemans, Boel De Paepe, Jan De Bleecker, et al.
Archives of Neurology|August 16, 2006
A novel mitochondrial transfer RNA(Asn) mutation causing multiorgan failureAnn Meulemans, Sara Seneca, Lieven Lagae, et al.
Pageof 5