paule Bénit
paule Bénit
research ingenieur INSERM
Verified email at inserm.fr
Title
Cited by
Cited by
Year
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
9651992
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
6821997
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
6442004
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
6402010
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
5252013
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
3892011
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
3852007
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
2682001
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
2422015
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
2292009
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
2062007
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
2042005
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
2012002
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
1952004
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
1812003
Life with or without AIF
E Hangen, K Blomgren, P Bénit, G Kroemer, N Modjtahedi
Trends in biochemical sciences 35 (5), 278-287, 2010
1712010
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
1562003
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
1492005
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
1452018
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
1242003
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