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Acetoacetate protects macrophages from lactic acidosis-induced mitochondrial dysfunction by metabolic reprograming.
Published in:
Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-27426-x
By:
- Adam, Clément;
- Paolini, Léa;
- Gueguen, Naïg;
- Mabilleau, Guillaume;
- Preisser, Laurence;
- Blanchard, Simon;
- Pignon, Pascale;
- Manero, Florence;
- Le Mao, Morgane;
- Morel, Alain;
- Reynier, Pascal;
- Beauvillain, Céline;
- Delneste, Yves;
- Procaccio, Vincent;
- Jeannin, Pascale
Publication type:
Article
Phostine 3.1a as a pharmacological compound with antiangiogenic properties against diseases with excess vascularization.
Published in:
FASEB Journal, 2019, v. 33, n. 5, p. 5864, doi. 10.1096/fj.201801450RRR
By:
- Bousseau, Simon;
- Marchand, Marion;
- Soleti, Raffaella;
- Vergori, Luisa;
- Hilairet, Grégory;
- Recoquillon, Sylvain;
- Le Mao, Morgane;
- Gueguen, Naig;
- Khiati, Salim;
- Clarion, Ludovic;
- Bakalara, Norbert;
- Martinez, M. Carmen;
- Germain, Stéphane;
- Lenaers, Guy;
- Andriantsitohaina, Ramaroson
Publication type:
Article
The Metabolomic Bioenergetic Signature of Opa1-Disrupted Mouse Embryonic Fibroblasts Highlights Aspartate Deficiency.
Published in:
Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-29972-9
By:
- Bocca, Cinzia;
- Kane, Mariame Selma;
- Veyrat-Durebex, Charlotte;
- Chupin, Stéphanie;
- Alban, Jennifer;
- Kouassi Nzoughet, Judith;
- Le Mao, Morgane;
- Chao de la Barca, Juan Manuel;
- Amati-Bonneau, Patrizia;
- Bonneau, Dominique;
- Procaccio, Vincent;
- Lenaers, Guy;
- Simard, Gilles;
- Chevrollier, Arnaud;
- Reynier, Pascal
Publication type:
Article
Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencing.
Published in:
Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2023.1259826
By:
- Gouiza, Ismail;
- Hechmi, Meriem;
- Zioudi, Abir;
- Dallali, Hamza;
- Kheriji, Nadia;
- Charif, Majida;
- Le Mao, Morgane;
- Galai, Said;
- Kraoua, Lilia;
- Youssef-Turki, Ilhem Ben;
- Kraoua, Ichraf;
- Lenaers, Guy;
- Kefi, Rym
Publication type:
Article
Author Correction: Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology.
Published in:
2020
By:
- Elouej, Sahar;
- Harhouri, Karim;
- Mao, Morgane Le;
- Baujat, Genevieve;
- Nampoothiri, Sheela;
- Kayserili, Hϋlya;
- Menabawy, Nihal Al;
- Selim, Laila;
- Paneque, Arianne Llamos;
- Kubisch, Christian;
- Lessel, Davor;
- Rubinsztajn, Robert;
- Charar, Chayki;
- Bartoli, Catherine;
- Airault, Coraline;
- Deleuze, Jean-François;
- Rötig, Agnes;
- Bauer, Peter;
- Pereira, Catarina;
- Loh, Abigail
Publication type:
Correction Notice
Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology.
Published in:
Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-18146-9
By:
- Elouej, Sahar;
- Harhouri, Karim;
- Le Mao, Morgane;
- Baujat, Genevieve;
- Nampoothiri, Sheela;
- Kayserili, Hϋlya;
- Menabawy, Nihal Al;
- Selim, Laila;
- Paneque, Arianne Llamos;
- Kubisch, Christian;
- Lessel, Davor;
- Rubinsztajn, Robert;
- Charar, Chayki;
- Bartoli, Catherine;
- Airault, Coraline;
- Deleuze, Jean-François;
- Rötig, Agnes;
- Bauer, Peter;
- Pereira, Catarina;
- Loh, Abigail
Publication type:
Article

Found: 6

Acetoacetate protects macrophages from lactic acidosis-induced mitochondrial dysfunction by metabolic reprograming.

Phostine 3.1a as a pharmacological compound with antiangiogenic properties against diseases with excess vascularization.

The Metabolomic Bioenergetic Signature of Opa1-Disrupted Mouse Embryonic Fibroblasts Highlights Aspartate Deficiency.

Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencing.

Author Correction: Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology.

Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology.