Works by Lacas-Gervais, Sandra

Results: 39
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    Evidences of a Direct Relationship between Cellular Fuel Supply and Ciliogenesis Regulated by Hypoxic VDAC1-ΔC.

    Published in:
    Cancers, 2020, v. 12, n. 11, p. 3484, doi. 10.3390/cancers12113484
    By:
    • Meyenberg Cunha-de Padua, Monique;
    • Fabbri, Lucilla;
    • Dufies, Maeva;
    • Lacas-Gervais, Sandra;
    • Contenti, Julie;
    • Voyton, Charles;
    • Fazio, Sofia;
    • Irondelle, Marie;
    • Mograbi, Baharia;
    • Rouleau, Matthieu;
    • Sadaghianloo, Nirvana;
    • Rovini, Amandine;
    • Brenner, Catherine;
    • Craigen, William J.;
    • Bourgeais, Jérôme;
    • Herault, Olivier;
    • Bost, Frédéric;
    • Mazure, Nathalie M.
    Publication type:
    Article
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    Accumulation of amyloid precursor protein C-terminal fragments triggers mitochondrial structure, function, and mitophagy defects in Alzheimer's disease models and human brains.

    Published in:
    Acta Neuropathologica, 2021, v. 141, n. 1, p. 39, doi. 10.1007/s00401-020-02234-7
    By:
    • Vaillant-Beuchot, Loan;
    • Mary, Arnaud;
    • Pardossi-Piquard, Raphaëlle;
    • Bourgeois, Alexandre;
    • Lauritzen, Inger;
    • Eysert, Fanny;
    • Kinoshita, Paula Fernanda;
    • Cazareth, Julie;
    • Badot, Céline;
    • Fragaki, Konstantina;
    • Bussiere, Renaud;
    • Martin, Cécile;
    • Mary, Rosanna;
    • Bauer, Charlotte;
    • Pagnotta, Sophie;
    • Paquis-Flucklinger, Véronique;
    • Buée-Scherrer, Valérie;
    • Buée, Luc;
    • Lacas-Gervais, Sandra;
    • Checler, Frédéric
    Publication type:
    Article
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    Mitochondrial defect in muscle precedes neuromuscular junction degeneration and motor neuron death in CHCHD10<sup>S59L/+</sup> mouse.

    Published in:
    Acta Neuropathologica, 2019, v. 138, n. 1, p. 123, doi. 10.1007/s00401-019-01988-z
    By:
    • Genin, Emmanuelle C.;
    • Bannwarth, Sylvie;
    • Fragaki, Konstantina;
    • Mauri-Crouzet, Alessandra;
    • Lespinasse, Françoise;
    • Neveu, Julien;
    • Ropert, Baptiste;
    • Augé, Gaelle;
    • Cochaud, Charlotte;
    • Paquis-Flucklinger, Véronique;
    • Madji Hounoum, Blandine;
    • Ricci, Jean-Ehrland;
    • Lacas-Gervais, Sandra;
    • Lefebvre-Omar, Cynthia;
    • Bigou, Stéphanie;
    • Chiot, Aude;
    • Boillée, Séverine;
    • Lobsiger, Christian S.;
    • Bohl, Delphine;
    • Mochel, Fanny
    Publication type:
    Article
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    Knockout of Vdac1 activates hypoxia-inducible factor through reactive oxygen species generation and induces tumor growth by promoting metabolic reprogramming and inflammation.

    Published in:
    Cancer & Metabolism, 2015, v. 3, n. 1, p. 1, doi. 10.1186/s40170-015-0133-5
    By:
    • Brahimi-Horn, M. Christiane;
    • Giuliano, Sandy;
    • Saland, Estelle;
    • Lacas-Gervais, Sandra;
    • Sheiko, Tatiana;
    • Pelletier, Joffrey;
    • Bourget, Isabelle;
    • Bost, Frédéric;
    • Féral, Chloé;
    • Boulter, Etienne;
    • Tauc, Michel;
    • Ivan, Mircea;
    • Garmy-Susini, Barbara;
    • Popa, Alexandra;
    • Mari, Bernard;
    • Sarry, Jean-Emmanuel;
    • Craigen, William J.;
    • Pouysségur, Jacques;
    • Mazure, Nathalie M.
    Publication type:
    Article
    9

    Bax Inhibitor-1 preserves pancreatic β-cell proteostasis by limiting proinsulin misfolding and programmed cell death.

    Published in:
    Cell Death & Disease, 2024, v. 15, n. 5, p. 1, doi. 10.1038/s41419-024-06701-x
    By:
    • Blanc, Marina;
    • Habbouche, Lama;
    • Xiao, Peng;
    • Lebeaupin, Cynthia;
    • Janona, Marion;
    • Vaillant, Nathalie;
    • Irondelle, Marie;
    • Gilleron, Jérôme;
    • Murcy, Florent;
    • Rousseau, Déborah;
    • Luci, Carmelo;
    • Barouillet, Thibault;
    • Marchetti, Sandrine;
    • Lacas-Gervais, Sandra;
    • Yvan-Charvet, Laurent;
    • Gual, Philippe;
    • Cardozo, Alessandra K.;
    • Bailly-Maitre, Béatrice
    Publication type:
    Article
    10

    CHCHD10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis.

    Published in:
    EMBO Molecular Medicine, 2016, v. 8, n. 1, p. 58, doi. 10.15252/emmm.201505496
    By:
    • Genin, Emmanuelle C;
    • Plutino, Morgane;
    • Bannwarth, Sylvie;
    • Villa, Elodie;
    • Cisneros‐Barroso, Eugenia;
    • Roy, Madhuparna;
    • Ortega‐Vila, Bernardo;
    • Fragaki, Konstantina;
    • Lespinasse, Françoise;
    • Pinero‐Martos, Estefania;
    • Augé, Gaëlle;
    • Moore, David;
    • Burté, Florence;
    • Lacas‐Gervais, Sandra;
    • Kageyama, Yusuke;
    • Itoh, Kie;
    • Yu‐Wai‐Man, Patrick;
    • Sesaki, Hiromi;
    • Ricci, Jean‐Ehrland;
    • Vives‐Bauza, Cristofol
    Publication type:
    Article
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    TMEM33 regulates intracellular calcium homeostasis in renal tubular epithelial cells.

    Published in:
    Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-10045-y
    By:
    • Arhatte, Malika;
    • Gunaratne, Gihan S.;
    • El Boustany, Charbel;
    • Kuo, Ivana Y.;
    • Moro, Céline;
    • Duprat, Fabrice;
    • Plaisant, Magali;
    • Duval, Hélène;
    • Li, Dahui;
    • Picard, Nicolas;
    • Couvreux, Anais;
    • Duranton, Christophe;
    • Rubera, Isabelle;
    • Pagnotta, Sophie;
    • Lacas-Gervais, Sandra;
    • Ehrlich, Barbara E.;
    • Marchant, Jonathan S.;
    • Savage, Aaron M.;
    • van Eeden, Fredericus J. M.;
    • Wilkinson, Robert N.
    Publication type:
    Article
    16

    Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from China.

    Published in:
    2016
    By:
    • Bannwarth, Sylvie;
    • Ait-El-Mkadem, Samira;
    • Chaussenot, Annabelle;
    • Genin, Emmanuelle C.;
    • Lacas-Gervais, Sandra;
    • Fragaki, Konstantina;
    • Berg-Alonso, Laetitia;
    • Kageyama, Yusuke;
    • Serre, Valérie;
    • Moore, David;
    • Verschueren, Annie;
    • Rouzier, Cécile;
    • Ber, Isabelle Le;
    • Augé, Gaëlle;
    • Cochaud, Charlotte;
    • Lespinasse, Françoise;
    • N'Guyen, Karine;
    • de Septenville, Anne;
    • Brice, Alexis;
    • Yu-Wai-Man, Patrick
    Publication type:
    Letter
    17

    Reply: Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?

    Published in:
    2015
    By:
    • Bannwarth, Sylvie;
    • Ait-El-Mkadem, Samira;
    • Chaussenot, Annabelle;
    • Genin, Emmanuelle C;
    • Lacas-Gervais, Sandra;
    • Fragaki, Konstantina;
    • Berg-Alonso, Laetitia;
    • Kageyama, Yusuke;
    • Serre, Valérie;
    • Moore, David;
    • Verschueren, Annie;
    • Rouzier, Cécile;
    • Le Ber, Isabelle;
    • Augé, Gaëlle;
    • Cochaud, Charlotte;
    • Lespinasse, Françoise;
    • N'Guyen, Karine;
    • de Septenville, Anne;
    • Brice, Alexis;
    • Yu-Wai-Man, Patrick
    Publication type:
    Letter
    18

    Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?

    Published in:
    2015
    By:
    • Dobson-Stone, Carol;
    • Shaw, Alex D.;
    • Hallupp, Marianne;
    • Bartley, Lauren;
    • McCann, Heather;
    • Brooks, William S.;
    • Loy, Clement T.;
    • Schofield, Peter R.;
    • Mather, Karen A.;
    • Kochan, Nicole A.;
    • Sachdev, Perminder S.;
    • Halliday, Glenda M.;
    • Piguet, Olivier;
    • Hodges, John R.;
    • Kwok, John B. J.;
    • Bannwarth, Sylvie;
    • Ait-El-Mkadem, Samira;
    • Chaussenot, Annabelle;
    • Genin, Emmanuelle C.;
    • Lacas-Gervais, Sandra
    Publication type:
    commentary
    19

    Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation.

    Published in:
    2015
    By:
    • Bannwarth, Sylvie;
    • Ait-El-Mkadem, Samira;
    • Chaussenot, Annabelle;
    • Genin, Emmanuelle C.;
    • Lacas-Gervais, Sandra;
    • Fragaki, Konstantina;
    • Berg-Alonso, Laetitia;
    • Kageyama, Yusuke;
    • Serre, Valérie;
    • Moore, David;
    • Verschueren, Annie;
    • Rouzier, Cécile;
    • Le Ber, Isabel;
    • Auge, Gaëlle;
    • Cochaud, Charlotte;
    • Lespinasse, Françoise;
    • N'Guyen, Karine;
    • de Septenville, Anne;
    • Brice, Alexis;
    • Yu-Wai-Man, Patrick
    Publication type:
    journal article
    20

    Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis.

    Published in:
    2015
    By:
    • Bannwarth, Sylvie;
    • Ait-El-Mkadem, Samira;
    • Chaussenot, Annabelle;
    • Genin, Emmanuelle C.;
    • Lacas-Gervais, Sandra;
    • Fragaki, Konstantina;
    • Berg-Alonso, Laetitia;
    • Kageyama, Yusuke;
    • Serre, Valérie;
    • Moore, David;
    • Verschueren, Annie;
    • Rouzier, Cécile;
    • le Le Ber, Isabel;
    • Augé, Gaëlle;
    • Cochaud, Charlotte;
    • Lespinasse, Francoise;
    • N'Guyen, Karine;
    • de Septenville, Anne;
    • Brice, Alexis;
    • Yu-Wai-Man, Patrick
    Publication type:
    journal article
    21

    Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis.

    Published in:
    Brain: A Journal of Neurology, 2014, v. 137, n. 12, p. e312, doi. 10.1093/brain/awu267
    By:
    • Bannwarth, Sylvie;
    • Ait-El-Mkadem, Samira;
    • Chaussenot, Annabelle;
    • Genin, Emmanuelle C.;
    • Lacas-Gervais, Sandra;
    • Fragaki, Konstantina;
    • Berg-Alonso, Laetitia;
    • Kageyama, Yusuke;
    • Serre, Valérie;
    • Moore, David;
    • Verschueren, Annie;
    • Rouzier, Cécile;
    • Le Ber, Isabelle;
    • Augé, Gaëlle;
    • Cochaud, Charlotte;
    • Lespinasse, Françoise;
    • N’Guyen, Karine;
    • de Septenville, Anne;
    • Brice, Alexis;
    • Yu-Wai-Man, Patrick
    Publication type:
    Article
    22

    Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease.

    Published in:
    Brain: A Journal of Neurology, 2014, v. 137, n. 12, p. e310, doi. 10.1093/brain/awu228
    By:
    • Bannwarth, Sylvie;
    • Ait-El-Mkadem, Samira;
    • Chaussenot, Annabelle;
    • Genin, Emmanuelle C.;
    • Lacas-Gervais, Sandra;
    • Fragaki, Konstantina;
    • Berg-Alonso, Laetitia;
    • Kageyama, Yusuke;
    • Serre, Valérie;
    • Moore, David;
    • Verschueren, Annie;
    • Rouzier, Cécile;
    • Le Ber, Isabelle;
    • Augé, Gaëlle;
    • Cochaud, Charlotte;
    • Lespinasse, Françoise;
    • N’Guyen, Karine;
    • de Septenville, Anne;
    • Brice, Alexis;
    • Yu-Wai-Man, Patrick
    Publication type:
    Article
    23

    Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?

    Published in:
    Brain: A Journal of Neurology, 2014, v. 137, n. 12, p. e314, doi. 10.1093/brain/awu300
    By:
    • Bannwarth, Sylvie;
    • Ait-El-Mkadem, Samira;
    • Chaussenot, Annabelle;
    • Genin, Emmanuelle C.;
    • Lacas-Gervais, Sandra;
    • Fragaki, Konstantina;
    • Berg-Alonso, Laetitia;
    • Kageyama, Yusuke;
    • Serre, Valérie;
    • Moore, David;
    • Verschueren, Annie;
    • Rouzier, Cécile;
    • Le Ber, Isabelle;
    • Augé, Gaëlle;
    • Cochaud, Charlotte;
    • Lespinasse, Françoise;
    • N’Guyen, Karine;
    • de Septenville, Anne;
    • Brice, Alexis;
    • Yu-Wai-Man, Patrick
    Publication type:
    Article
    24

    A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement.

    Published in:
    Brain: A Journal of Neurology, 2014, v. 137, n. 8, p. 2329, doi. 10.1093/brain/awu138
    By:
    • Bannwarth, Sylvie;
    • Ait-El-Mkadem, Samira;
    • Chaussenot, Annabelle;
    • Genin, Emmanuelle C.;
    • Lacas-Gervais, Sandra;
    • Fragaki, Konstantina;
    • Berg-Alonso, Laetitia;
    • Kageyama, Yusuke;
    • Serre, Valérie;
    • Moore, David G.;
    • Verschueren, Annie;
    • Rouzier, Cécile;
    • Le Ber, Isabelle;
    • Augé, Gaëlle;
    • Cochaud, Charlotte;
    • Lespinasse, Françoise;
    • N’Guyen, Karine;
    • de Septenville, Anne;
    • Brice, Alexis;
    • Yu-Wai-Man, Patrick
    Publication type:
    Article
    25

    Local Mitochondrial-Endolysosomal Microfusion Cleaves Voltage-Dependent Anion Channel 1 To Promote Survival in Hypoxia.

    Published in:
    Molecular & Cellular Biology, 2015, v. 35, n. 9, p. 1491, doi. 10.1128/MCB.01402-14
    By:
    • Brahimi-Horn, M. Christiane;
    • Lacas-Gervais, Sandra;
    • Adaixo, Ricardo;
    • Ilc, Karine;
    • Rouleau, Matthieu;
    • Notte, Annick;
    • Dieu, Marc;
    • Michiels, Carine;
    • Voeltzel, Thibault;
    • Maguer-Satta, Véronique;
    • Pelletier, Joffrey;
    • Ilie, Marius;
    • Hofman, Paul;
    • Manoury, Bénédicte;
    • Schmidt, Alexander;
    • Hiller, Sebastian;
    • Pouysségur, Jacques;
    • Mazure, Nathalie M.
    Publication type:
    Article
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    A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca<sup>2+</sup> homeostasis and ER-mitochondria interactions.

    Published in:
    Human Molecular Genetics, 2017, v. 26, n. 9, p. 1599, doi. 10.1093/hmg/ddx060
    By:
    • Rouzier, Cécile;
    • Moore, David;
    • Delorme, Cécile;
    • Lacas-Gervais, Sandra;
    • Ait-El-Mkadem, Samira;
    • Fragaki, Konstantina;
    • Burté, Florence;
    • Serre, Valérie;
    • Bannwarth, Sylvie;
    • Chaussenot, Annabelle;
    • Catala, Martin;
    • Yu-Wai-Man, Patrick;
    • Paquis-Flucklinger, Véronique
    Publication type:
    Article
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    The Inactivation of <i>Arx</i> in Pancreatic α-Cells Triggers Their Neogenesis and Conversion into Functional β-Like Cells.

    Published in:
    PLoS Genetics, 2013, v. 9, n. 10, p. 1, doi. 10.1371/journal.pgen.1003934
    By:
    • Courtney, Monica;
    • Gjernes, Elisabet;
    • Druelle, Noémie;
    • Ravaud, Christophe;
    • Vieira, Andhira;
    • Ben-Othman, Nouha;
    • Pfeifer, Anja;
    • Avolio, Fabio;
    • Leuckx, Gunter;
    • Lacas-Gervais, Sandra;
    • Burel-Vandenbos, Fanny;
    • Ambrosetti, Damien;
    • Hecksher-Sorensen, Jacob;
    • Ravassard, Philippe;
    • Heimberg, Harry;
    • Mansouri, Ahmed;
    • Collombat, Patrick
    Publication type:
    Article
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    Transcription- and phosphorylation-dependent control of a functional interplay between XBP1s and PINK1 governs mitophagy and potentially impacts Parkinson disease pathophysiology.

    Published in:
    Autophagy, 2021, v. 17, n. 12, p. 4363, doi. 10.1080/15548627.2021.1917129
    By:
    • El Manaa, Wejdane;
    • Duplan, Eric;
    • Goiran, Thomas;
    • Lauritzen, Inger;
    • Vaillant Beuchot, Loan;
    • Lacas-Gervais, Sandra;
    • Morais, Vanessa Alexandra;
    • You, Han;
    • Qi, Ling;
    • Salazar, Mario;
    • Ozcan, Umut;
    • Chami, Mounia;
    • Checler, Frédéric;
    • Alves da Costa, Cristine
    Publication type:
    Article
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    REDD1 deficiency protects against nonalcoholic hepatic steatosis induced by high‐fat diet.

    Published in:
    FASEB Journal, 2020, v. 34, n. 4, p. 5046, doi. 10.1096/fj.201901799RR
    By:
    • Dumas, Karine;
    • Ayachi, Chaima;
    • Gilleron, Jerome;
    • Lacas‐Gervais, Sandra;
    • Pastor, Faustine;
    • Favier, François B.;
    • Peraldi, Pascal;
    • Vaillant, Nathalie;
    • Yvan‐Charvet, Laurent;
    • Bonnafous, Stéphanie;
    • Patouraux, Stéphanie;
    • Anty, Rodolphe;
    • Tran, Albert;
    • Gual, Philippe;
    • Cormont, Mireille;
    • Tanti, Jean‐François;
    • Giorgetti‐Peraldi, Sophie
    Publication type:
    Article