Showing results (161-170 of 214) with videos related to

Sort By:
Pageof 22
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.
Scientific Reports|March 19, 2021
Long-term treated HIV infection is associated with platelet mitochondrial dysfunctionWouter A van der Heijden, Lisa van de Wijer, Martin Jaeger, et al.
Translational Psychiatry|June 4, 2020
Impaired mitochondrial complex I function as a candidate driver in the biological stress response and a concomitant stress-induced brain metabolic reprogramming in male miceTim L Emmerzaal, Graeme Preston, Bram Geenen, et al.
American Journal of Human Genetics|January 31, 2012
Lack of the mitochondrial protein acylglycerol kinase causes Sengers syndromeJohannes A Mayr, Tobias B Haack, Elisabeth Graf, et al.
Journal of Inherited Metabolic Disease|May 31, 2012
Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 casesS Koene, R J Rodenburg, M S van der Knaap, et al.
Pageof 22