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Richard J Rodenburg

Showing results (81-90 of 137) with videos related to

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European Journal of Medical Genetics|November 14, 2018
Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11Karit Reinson, Reka Kovacs-Nagy, Eve Õiglane-Shlik, et al.
European Journal of Pediatrics|September 8, 2006
Multiple oxidative phosphorylation deficiencies in severe childhood multi-system disorders due to polymerase gamma (POLG1) mutationsMaaike C de Vries, Richard J Rodenburg, Eva Morava, et al.
Journal of the American College of Cardiology|April 5, 2023
Prolonged Moderate-Intensity Exercise Does Not Increase Muscle Injury Markers in Symptomatic or Asymptomatic Statin UsersNeeltje A E Allard, Lando Janssen, Bart Lagerwaard, et al.
American Journal of Human Genetics|June 3, 2008
NDUFA2 complex I mutation leads to Leigh diseaseSaskia J G Hoefs, Cindy E J Dieteren, Felix Distelmaier, et al.
Plos Biology|October 9, 2019
Correction: Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neuronsNaila Haq, Christoph Schmidt-Hieber, Fernando J Sialana, et al.
Plos Biology|September 4, 2019
Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neuronsNaila Haq, Christoph Schmidt-Hieber, Fernando J Sialana, et al.
American Journal of Human Genetics|July 5, 2016
Mutations in Complex I Assembly Factor TMEM126B Result in Muscle Weakness and Isolated Complex I DeficiencyLaura Sánchez-Caballero, Benedetta Ruzzenente, Lucas Bianchi, et al.
Human Molecular Genetics|July 11, 2014
A mutation in the human CBP4 ortholog UQCC3 impairs complex III assembly, activity and cytochrome b stabilityBas F J Wanschers, Radek Szklarczyk, Mariël A M van den Brand, et al.
Neurology|April 5, 2013
NUBPL mutations in patients with complex I deficiency and a distinct MRI patternSietske H Kevelam, Richard J Rodenburg, Nicole I Wolf, et al.
Cell Metabolism|September 3, 2015
Statin-Induced Myopathy Is Associated with Mitochondrial Complex III InhibitionTom J J Schirris, G Herma Renkema, Tina Ritschel, et al.
Pageof 14

Showing results (81-90 of 137) with videos related to

Sort By:
Pageof 14
European Journal of Medical Genetics|November 14, 2018
Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11Karit Reinson, Reka Kovacs-Nagy, Eve Õiglane-Shlik, et al.
European Journal of Pediatrics|September 8, 2006
Multiple oxidative phosphorylation deficiencies in severe childhood multi-system disorders due to polymerase gamma (POLG1) mutationsMaaike C de Vries, Richard J Rodenburg, Eva Morava, et al.
Journal of the American College of Cardiology|April 5, 2023
Prolonged Moderate-Intensity Exercise Does Not Increase Muscle Injury Markers in Symptomatic or Asymptomatic Statin UsersNeeltje A E Allard, Lando Janssen, Bart Lagerwaard, et al.
American Journal of Human Genetics|June 3, 2008
NDUFA2 complex I mutation leads to Leigh diseaseSaskia J G Hoefs, Cindy E J Dieteren, Felix Distelmaier, et al.
Plos Biology|October 9, 2019
Correction: Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neuronsNaila Haq, Christoph Schmidt-Hieber, Fernando J Sialana, et al.
Plos Biology|September 4, 2019
Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neuronsNaila Haq, Christoph Schmidt-Hieber, Fernando J Sialana, et al.
American Journal of Human Genetics|July 5, 2016
Mutations in Complex I Assembly Factor TMEM126B Result in Muscle Weakness and Isolated Complex I DeficiencyLaura Sánchez-Caballero, Benedetta Ruzzenente, Lucas Bianchi, et al.
Human Molecular Genetics|July 11, 2014
A mutation in the human CBP4 ortholog UQCC3 impairs complex III assembly, activity and cytochrome b stabilityBas F J Wanschers, Radek Szklarczyk, Mariël A M van den Brand, et al.
Neurology|April 5, 2013
NUBPL mutations in patients with complex I deficiency and a distinct MRI patternSietske H Kevelam, Richard J Rodenburg, Nicole I Wolf, et al.
Cell Metabolism|September 3, 2015
Statin-Induced Myopathy Is Associated with Mitochondrial Complex III InhibitionTom J J Schirris, G Herma Renkema, Tina Ritschel, et al.
Pageof 14