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Journal of Applied Physiology (Bethesda, Md. : 1985)|May 25, 2018
Mitochondrial complex I defect resulting from exercise-induced lower limb ischemia in patients with peripheral arterial diseaseI Signolet, P Abraham, S Chupin, et al.
Human Reproduction (Oxford, England)|January 13, 2017
The mitochondrial DNA content of cumulus granulosa cells is linked to embryo qualityV Desquiret-Dumas, A Clément, V Seegers, et al.
Vascular Pharmacology|October 17, 2015
Estrogens are needed for the improvement in endothelium-mediated dilation induced by a chronic increase in blood flow in rat mesenteric arteriesK Tarhouni, A L Guihot, E Vessieres, et al.
Nanoscale|April 1, 2015
Impact of anatase and rutile titanium dioxide nanoparticles on uptake carriers and efflux pumps in Caco-2 gut epithelial cellsM Dorier, E Brun, G Veronesi, et al.
American Journal of Medical Genetics. Part A|June 15, 2007
Identification of novel mutations in WFS1 and genotype-phenotype correlation in Wolfram syndromeA Cano, C Rouzier, S Monnot, et al.
Nanoimpact|March 9, 2026
Toxicity of polycaprolactone nanoplastics, pristine or weathered in environmental conditions, to human intestinal epithelial cells, in vitroM Boulée, V Bard, M Papin, et al.
Human Reproduction (Oxford, England)|May 22, 2015
Relationship between diminished ovarian reserve and mitochondrial biogenesis in cumulus cellsL Boucret, J M Chao de la Barca, C Morinière, et al.
Eye (London, England)|November 19, 2016
Multiethnic involvement in autosomal-dominant optic atrophy in SingaporeJ L Loo, S Singhal, A V Rukmini, et al.
The Journal of Clinical Investigation|July 7, 1999
Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblastsV Procaccio, B Mousson, R Beugnot, et al.
Diabetes & Metabolism|October 29, 2008
Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitisC Verny, P Amati-Bonneau, F Letournel, et al.
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