C. Angebault

发表

Metformin Reverses the Enhanced Myocardial SR/ER–Mitochondria Interaction and Impaired Complex I-Driven Respiration in Dystrophin-Deficient Mice

J. Rieusset, A. Lacampagne, J. Fauconnier, 2021, Frontiers in Cell and Developmental Biology.

Light action spectrum on oxidative stress and mitochondrial damage in A2E-loaded retinal pigment epithelium cells

J. Sahel, S. Picaud, G. Lenaers, 2018, Cell Death & Disease.

Mitochondrial oxidative stress induces leaky ryanodine receptor during mechanical ventilation.

S. Jaber, S. Matecki, S. Reiken, 2019, Free radical biology & medicine.

The human OPA1delTTAG mutation induces premature age-related systemic neurodegeneration in mouse.

N. Boddaert, J. Renou, Jing Wang, 2012, Brain : a journal of neurology.

LIX1-mediated changes in mitochondrial metabolism control the fate of digestive mesenchyme-derived cells

A. Mourier, A. Lacampagne, P. de Santa Barbara, 2022, Redox biology.

Mutations in DNM1L, as in OPA1, result indominant optic atrophy despite opposite effectson mitochondrial fusion and fission

N. Boddaert, Majida Charif, D. Bonneau, 2017, Brain : a journal of neurology.

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.

Increased steroidogenesis promotes early-onset and severe vision loss in females with OPA1 dominant optic atrophy.

M. Larsen, D. Milea, G. Lenaers, 2016, Human molecular genetics.

Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies.

B. Lorenz, P. Chinnery, P. Yu-Wai-Man, 2015, American Journal of Human Genetics.

Idebenone increases mitochondrial complex I activity in fibroblasts from LHON patients while producing contradictory effects on respiration

D. Milea, V. Desquiret-Dumas, D. Bonneau, 2011, BMC Research Notes.

Light action spectrum on oxidative stress and mitochondrial damage in A2E-loaded retinal pigment epithelium cells

J. Sahel, S. Picaud, G. Lenaers, 2018, Cell Death & Disease.

Phloroglucinol protects retinal pigment epithelium and photoreceptor against all‐trans‐retinal–induced toxicity and inhibits A2E formation

P. Brabet, C. Hamel, Aurélie Cubizolle, 2016, Journal of cellular and molecular medicine.

ER-mitochondria cross-talk is regulated by the Ca2+ sensor NCS1 and is impaired in Wolfram syndrome

B. Delprat, D. Milea, M. Thiry, 2018, Science Signaling.

LIX1 controls digestive mesenchyme-derived cell fate decision by regulating cristae organization in mitochondria

N. Taylor, A. Lacampagne, P. de Santa Barbara, 2022, bioRxiv.

Mutation in NDUFA13/GRIM19 leads to early onset hypotonia, dyskinesia and sensorial deficiencies, and mitochondrial complex I instability.

F. Rivier, Majida Charif, G. Lenaers, 2015, Human molecular genetics.

Increased steroidogenesis promotes early-onset and severe vision loss in females with OPA1 dominant optic atrophy.

M. Larsen, D. Milea, G. Lenaers, 2017, Human molecular genetics.

Loss of function of Ywhah in mice induces deafness and cochlear outer hair cells' degeneration

G. Rebillard, B. Delprat, P. Chinnery, 2016, Cell Death Discovery.