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Human Molecular Genetics|July 6, 2019
Deregulating mitochondrial metabolite and ion transport has beneficial effects in yeast and human cellular models for NARP syndromeXin Su, Malgorzata Rak, Emmanuel Tetaud, et al.
Orphanet Journal of Rare Diseases|October 31, 2019
Arabidopsis thaliana alternative dehydrogenases: a potential therapy for mitochondrial complex I deficiency? Perspectives and pitfallsAlessia Catania, Arcangela Iuso, Juliette Bouchereau, et al.
Cell Death & Disease|October 28, 2016
ZIKA virus elicits P53 activation and genotoxic stress in human neural progenitors similar to mutations involved in severe forms of genetic microcephalyVincent El Ghouzzi, Federico T Bianchi, Ivan Molineris, et al.
Cell Death & Disease|November 22, 2018
Correction to: ZIKA virus elicits P53 activation and genotoxic stress in human neural progenitors similar to mutations involved in severe forms of genetic microcephalyVincent El Ghouzzi, Federico T Bianchi, Ivan Molineris, et al.
Annals of Neurology|January 13, 2019
SLC13A3 variants cause acute reversible leukoencephalopathy and α-ketoglutarate accumulationJoseph P Dewulf, Elsa Wiame, Imen Dorboz, et al.
American Journal of Human Genetics|August 6, 2013
Mutations in CYC1, encoding cytochrome c1 subunit of respiratory chain complex III, cause insulin-responsive hyperglycemiaPauline Gaignard, Minal Menezes, Manuel Schiff, et al.
Stem Cell Reports|May 10, 2023
Depletion of WFS1 compromises mitochondrial function in hiPSC-derived neuronal models of Wolfram syndromeMalgorzata Zatyka, Tatiana R Rosenstock, Congxin Sun, et al.
Cell Research|May 29, 2019
AIF-regulated oxidative phosphorylation supports lung cancer developmentShuan Rao, Laura Mondragón, Blanka Pranjic, et al.
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