paule Bénit
paule Bénit
research ingenieur INSERM
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Cited by
Cited by
The complete DNA sequence of yeast chromosome III
SG Oliver, QJM Van der Aart, ML Agostoni-Carbone, M Aigle, ...
Nature 357 (6373), 38-46, 1992
Mutations of the TWIST gene in the Saethre-Chotzene syndrome
V El Ghouzzi, M Le Merrer, F Perrin-Schmitt, E Lajeunie, P Benit, D Renier, ...
Nature genetics 15 (1), 42-46, 1997
AIF deficiency compromises oxidative phosphorylation
N Vahsen, C Candé, JJ Brière, P Bénit, N Joza, N Larochette, ...
The EMBO journal 23 (23), 4679-4689, 2004
SDHA is a tumor suppressor gene causing paraganglioma
N Burnichon, JJ Briere, R Libé, L Vescovo, J Riviere, F Tissier, E Jouanno, ...
Human molecular genetics 19 (15), 3011-3020, 2010
SDH mutations establish a hypermethylator phenotype in paraganglioma
E Letouzé, C Martinelli, C Loriot, N Burnichon, N Abermil, C Ottolenghi, ...
Cancer cell 23 (6), 739-752, 2013
Spermidine and resveratrol induce autophagy by distinct pathways converging on the acetylproteome
E Morselli, G Mariño, MV Bennetzen, T Eisenberg, E Megalou, ...
Journal of Cell Biology 192 (4), 615-629, 2011
Targeted deletion of AIF decreases mitochondrial oxidative phosphorylation and protects from obesity and diabetes
JA Pospisilik, C Knauf, N Joza, P Benit, M Orthofer, PD Cani, ...
Cell 131 (3), 476-491, 2007
Large-scale deletion and point mutations of the nuclear NDUFV1 and NDUFS1 genes in mitochondrial complex I deficiency
P Bénit, D Chretien, N Kadhom, P de Lonlay-Debeney, V Cormier-Daire, ...
The American Journal of Human Genetics 68 (6), 1344-1352, 2001
Imbalanced OPA1 processing and mitochondrial fragmentation cause heart failure in mice
T Wai, J García-Prieto, MJ Baker, C Merkwirth, P Benit, P Rustin, ...
Science 350 (6265), 2015
The Warburg effect is genetically determined in inherited pheochromocytomas
J Favier, JJ Brière, N Burnichon, J Rivière, L Vescovo, P Benit, ...
PloS one 4 (9), e7094, 2009
S6 kinase deletion suppresses muscle growth adaptations to nutrient availability by activating AMP kinase
V Aguilar, S Alliouachene, A Sotiropoulos, A Sobering, Y Athea, F Djouadi, ...
Cell metabolism 5 (6), 476-487, 2007
Muscle-specific loss of apoptosis-inducing factor leads to mitochondrial dysfunction, skeletal muscle atrophy, and dilated cardiomyopathy
N Joza, GY Oudit, D Brown, P Bénit, Z Kassiri, N Vahsen, L Benoit, ...
Molecular and cellular biology 25 (23), 10261-10272, 2005
Coenzyme Q10 and idebenone in the therapy of respiratory chain diseases: rationale and comparative benefits
V Geromel, N Darin, D Chrétien, P Bénit, P DeLonlay, A Rötig, A Munnich, ...
Molecular genetics and metabolism 77 (1-2), 21-30, 2002
Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome
P Benit, A Slama, F Cartault, I Giurgea, D Chretien, S Lebon, C Marsac, ...
Journal of medical genetics 41 (1), 14-17, 2004
Mutant NDUFV2 subunit of mitochondrial complex I causes early onset hypertrophic cardiomyopathy and encephalopathy
P Bénit, R Beugnot, D Chretien, I Giurgea, P De Lonlay‐Debeney, ...
Human mutation 21 (6), 582-586, 2003
Life with or without AIF
E Hangen, K Blomgren, P Bénit, G Kroemer, N Modjtahedi
Trends in biochemical sciences 35 (5), 278-287, 2010
The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency
M Chol, S Lebon, P Benit, D Chretien, P De Lonlay, A Goldenberg, ...
Journal of medical genetics 40 (3), 188-191, 2003
Mitochondrial succinate is instrumental for HIF1α nuclear translocation in SDHA-mutant fibroblasts under normoxic conditions
JJ Briere, J Favier, P Benit, VE Ghouzzi, A Lorenzato, D Rabier, ...
Human molecular genetics 14 (21), 3263-3269, 2005
Mitochondria are physiologically maintained at close to 50 C
D Chrétien, P Bénit, HH Ha, S Keipert, R El-Khoury, YT Chang, ...
PLoS biology 16 (1), e2003992, 2018
Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency
S Lebon, M Chol, P Benit, C Mugnier, D Chretien, I Giurgea, I Kern, ...
Journal of medical genetics 40 (12), 896-899, 2003
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