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Richard J Rodenburg

Showing results (31-40 of 137) with videos related to

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Proteomics|August 19, 2009
LC-MS/MS as an alternative for SDS-PAGE in blue native analysis of protein complexesHans J C T Wessels, Rutger O Vogel, Lambert van den Heuvel, et al.
European Journal of Human Genetics : EJHG|November 16, 2006
The mitochondrial 13513G > A mutation is most frequent in Leigh syndrome combined with reduced complex I activity, optic atrophy and/or Wolff-Parkinson-WhiteE Mariken Ruiter, Marloes H Siers, Christa van den Elzen, et al.
Pediatric Research|June 26, 2012
Fluorescence imaging of mitochondria in cultured skin fibroblasts: a useful method for the detection of oxidative phosphorylation defectsBoel De Paepe, Joél Smet, Arnaud Vanlander, et al.
Brain : a Journal of Neurology|April 2, 2009
Mitochondrial complex I deficiency: from organelle dysfunction to clinical diseaseFelix Distelmaier, Werner J H Koopman, Lambertus P van den Heuvel, et al.
JIMD Reports|September 30, 2016
RARS2 Mutations: Is Pontocerebellar Hypoplasia Type 6 a Mitochondrial Encephalopathy?Tessa van Dijk, Fred van Ruissen, Bregje Jaeger, et al.
Journal of Inherited Metabolic Disease|August 28, 2015
Increased mitochondrial ATP production capacity in brain of healthy mice and a mouse model of isolated complex I deficiency after isoflurane anesthesiaGanesh R Manjeri, Richard J Rodenburg, Lionel Blanchet, et al.
Neurogenetics|March 24, 2015
MRPL44 mutations cause a slowly progressive multisystem disease with childhood-onset hypertrophic cardiomyopathyFelix Distelmaier, Tobias B Haack, Claudia B Catarino, et al.
Annals of Clinical and Translational Neurology|October 31, 2014
Phenylbutyrate increases pyruvate dehydrogenase complex activity in cells harboring a variety of defectsRosa Ferriero, Audrey Boutron, Michele Brivet, et al.
BMC Cardiovascular Disorders|May 28, 2016
Primary skeletal muscle myoblasts from chronic heart failure patients exhibit loss of anti-inflammatory and proliferative activityTahnee Sente, An M Van Berendoncks, An I Jonckheere, et al.
Neurogenetics|February 10, 2015
MRPS22 mutation causes fatal neonatal lactic acidosis with brain and heart abnormalitiesFabian Baertling, Tobias B Haack, Richard J Rodenburg, et al.
Pageof 14

Showing results (31-40 of 137) with videos related to

Sort By:
Pageof 14
Proteomics|August 19, 2009
LC-MS/MS as an alternative for SDS-PAGE in blue native analysis of protein complexesHans J C T Wessels, Rutger O Vogel, Lambert van den Heuvel, et al.
European Journal of Human Genetics : EJHG|November 16, 2006
The mitochondrial 13513G > A mutation is most frequent in Leigh syndrome combined with reduced complex I activity, optic atrophy and/or Wolff-Parkinson-WhiteE Mariken Ruiter, Marloes H Siers, Christa van den Elzen, et al.
Pediatric Research|June 26, 2012
Fluorescence imaging of mitochondria in cultured skin fibroblasts: a useful method for the detection of oxidative phosphorylation defectsBoel De Paepe, Joél Smet, Arnaud Vanlander, et al.
Brain : a Journal of Neurology|April 2, 2009
Mitochondrial complex I deficiency: from organelle dysfunction to clinical diseaseFelix Distelmaier, Werner J H Koopman, Lambertus P van den Heuvel, et al.
JIMD Reports|September 30, 2016
RARS2 Mutations: Is Pontocerebellar Hypoplasia Type 6 a Mitochondrial Encephalopathy?Tessa van Dijk, Fred van Ruissen, Bregje Jaeger, et al.
Journal of Inherited Metabolic Disease|August 28, 2015
Increased mitochondrial ATP production capacity in brain of healthy mice and a mouse model of isolated complex I deficiency after isoflurane anesthesiaGanesh R Manjeri, Richard J Rodenburg, Lionel Blanchet, et al.
Neurogenetics|March 24, 2015
MRPL44 mutations cause a slowly progressive multisystem disease with childhood-onset hypertrophic cardiomyopathyFelix Distelmaier, Tobias B Haack, Claudia B Catarino, et al.
Annals of Clinical and Translational Neurology|October 31, 2014
Phenylbutyrate increases pyruvate dehydrogenase complex activity in cells harboring a variety of defectsRosa Ferriero, Audrey Boutron, Michele Brivet, et al.
BMC Cardiovascular Disorders|May 28, 2016
Primary skeletal muscle myoblasts from chronic heart failure patients exhibit loss of anti-inflammatory and proliferative activityTahnee Sente, An M Van Berendoncks, An I Jonckheere, et al.
Neurogenetics|February 10, 2015
MRPS22 mutation causes fatal neonatal lactic acidosis with brain and heart abnormalitiesFabian Baertling, Tobias B Haack, Richard J Rodenburg, et al.
Pageof 14