V. Desquiret

发表

Heme oxygenase-1 induction restores high-blood-flow-dependent remodeling and endothelial function in mesenteric arteries of old rats

S. Faure, V. Procaccio, D. Henrion, 2011, Journal of hypertension.

Mitochondrial dysfunction and pathophysiology of Charcot–Marie–Tooth disease involving GDAP1 mutations

D. Bonneau, P. Amati‐Bonneau, P. Reynier, 2011, Experimental Neurology.

Dinitrophenol-induced mitochondrial uncoupling in vivo triggers respiratory adaptation in HepG2 cells.

P. Ritz, D. Roussel, Y. Malthiéry, 2006, Biochimica et biophysica acta.

Bioenergetic defect associated with mKATP channel opening in a mouse model carrying a mitofusin 2 mutation

J. Martinou, D. Bonneau, P. Amati‐Bonneau, 2011, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Relationship between diminished ovarian reserve and mitochondrial biogenesis in cumulus cells.

P. Reynier, V. Procaccio, J. M. C. Barca, 2015, Human reproduction.

Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicity.

D. Bonneau, P. Amati‐Bonneau, P. Reynier, 2010, Mitochondrion.

Acute and late-onset optic atrophy due to a novel OPA1 mutation leading to a mitochondrial coupling defect

A. Toutain, D. Bonneau, P. Amati‐Bonneau, 2009, Molecular vision.

Mitochondrial macro-haplogroup JT may play a protective role in ovarian ageing.

P. Reynier, V. Procaccio, S. Lemerle, 2014, Mitochondrion.

Mitochondrial effects of dexamethasone imply both membrane and cytosolic-initiated pathways in HepG2 cells.

P. Ritz, G. Simard, Y. Malthiéry, 2008, The international journal of biochemistry & cell biology.

Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation.

D. Bonneau, P. Amati‐Bonneau, P. Reynier, 2011, Mitochondrion.

Heme Oxygenase 1 Is Differentially Involved in Blood Flow–Dependent Arterial Remodeling: Role of Inflammation, Oxidative Stress, and Nitric Oxide

V. Procaccio, D. Henrion, B. Toutain, 2011, Hypertension.

Bioenergetic defect associated with mKATP channel opening in a mouse model carrying a mitofusin 2 mutation

J. Martinou, D. Bonneau, P. Amati‐Bonneau, 2011, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.