Genotype–phenotype correlation in PRKN-associated Parkinson’s disease
Menon, Poornima Jayadev, Sambin, Sara, Criniere-Boizet, Baptiste, Courtin, Thomas, Tesson, Christelle, Casse, Fanny, Ferrien, Melanie, Mariani, Louise-Laure, Carvalho, Stephanie, Lejeune, Francois-Xavier, Rebbah, Sana, Martet, Gaspard, Houot, Marion, Lanore, Aymeric, Mangone, Graziella, Roze, Emmanuel, Vidailhet, Marie, Aasly, Jan, Gan Or, Ziv, Yu, Eric, Dauvilliers, Yves, Zimprich, Alexander, Tomantschger, Volker, Pirker, Walter, Álvarez, Ignacio, Pastor, Pau, Di Fonzo, Alessio, Bhatia, Kailash P., Magrinelli, Francesca, Houlden, Henry, Real, Raquel, Quattrone, Andrea, Limousin, Patricia, Korlipara, Prasad, Foltynie, Thomas, Grosset, Donald, Williams, Nigel, Narendra, Derek, Lin, Hsin-Pin, Jovanovic, Carna, Svetel, Marina, Lynch, Timothy, Gallagher, Amy, Vandenberghe, Wim, Gasser, Thomas, Brockmann, Kathrin, Morris, Huw R., Borsche, Max, Klein, Christine, Corti, Olga, Brice, Alexis, Lesage, Suzanne, Corvol, Jean Christophe
Published in NPJ Parkinson's Disease (29.03.2024)
Published in NPJ Parkinson's Disease (29.03.2024)
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Parkin deficiency delays motor decline and disease manifestation in a mouse model of synucleinopathy
Fournier, Margot, Vitte, Jérémie, Garrigue, Jérôme, Langui, Dominique, Dullin, Jean-Philippe, Saurini, Françoise, Hanoun, Naïma, Perez-Diaz, Fernando, Cornilleau, Fabien, Joubert, Chantal, Ardila-Osorio, Héctor, Traver, Sabine, Duchateau, René, Goujet-Zalc, Cécile, Paleologou, Katerina, Lashuel, Hilal A, Haass, Christian, Duyckaerts, Charles, Cohen-Salmon, Charles, Kahle, Philipp J, Hamon, Michel, Brice, Alexis, Corti, Olga
Published in PloS one (14.08.2009)
Published in PloS one (14.08.2009)
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The C289G and C418R missense mutations cause rapid sequestration of human Parkin into insoluble aggregates
Gu, Wen-Jie, Corti, Olga, Araujo, Francisco, Hampe, Cornelia, Jacquier, Sandrine, Lücking, Christoph B, Abbas, Nacer, Duyckaerts, Charles, Rooney, Thomas, Pradier, Laurent, Ruberg, Merle, Brice, Alexis
Published in Neurobiology of disease (01.12.2003)
Published in Neurobiology of disease (01.12.2003)
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Long-Term Doxycycline-Controlled Expression of Human Tyrosine Hydroxylase after Direct Adenovirus-Mediated Gene Transfer to a Rat Model of Parkinson's Disease
Corti, Olga, Sanchez-Capelo, Amelia, Colin, Philippe, Hanoun, Naima, Hamon, Michel, Mallet, Jacques
Published in Proceedings of the National Academy of Sciences - PNAS (12.10.1999)
Published in Proceedings of the National Academy of Sciences - PNAS (12.10.1999)
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From dysfunctional endoplasmic reticulum-mitochondria coupling to neurodegeneration
Erpapazoglou, Zoi, Mouton-Liger, François, Corti, Olga
Published in Neurochemistry international (01.10.2017)
Published in Neurochemistry international (01.10.2017)
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LRRK2 impairs PINK1/Parkin-dependent mitophagy via its kinase activity: pathologic insights into Parkinson's disease
Bonello, Fiona, Hassoun, Sidi-Mohamed, Mouton-Liger, François, Shin, Yea Seul, Muscat, Adeline, Tesson, Christelle, Lesage, Suzanne, Beart, Philip M, Brice, Alexis, Krupp, Johannes, Corvol, Jean-Christophe, Corti, Olga
Published in Human molecular genetics (15.05.2019)
Published in Human molecular genetics (15.05.2019)
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Promoting the clearance of neurotoxic proteins in neurodegenerative disorders of ageing
Boland, Barry, Yu, Wai Haung, Corti, Olga, Mollereau, Bertrand, Henriques, Alexandre, Bezard, Erwan, Pastores, Greg M., Rubinsztein, David C., Nixon, Ralph A., Duchen, Michael R., Mallucci, Giovanna R., Kroemer, Guido, Levine, Beth, Eskelinen, Eeva-Liisa, Mochel, Fanny, Spedding, Michael, Louis, Caroline, Martin, Olivier R., Millan, Mark J.
Published in Nature reviews. Drug discovery (01.09.2018)
Published in Nature reviews. Drug discovery (01.09.2018)
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Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
Lesage, Suzanne, Deramecourt, Vincent, Jacoupy, Maxime, Hassoun, Sidi Mohamed, Pujol, Claire, Maurage, Claude-Alain, Sahbatou, Mourad, Liebau, Stefan, Bilgic, Basar, Emre, Murat, Erginel-Unaltuna, Nihan, Guven, Gamze, Tison, François, Tranchant, Christine, Corvol, Jean-Christophe, Krack, Paul, Hernandez, Dena G., Gibbs, J. Raphael, Hardy, John, Wood, Nicholas W., Durr, Alexandra, Deleuze, Jean-François, Tazir, Meriem, Destée, Alain, Lohmann, Ebba, Corti, Olga, Brice, Alexis, Lesage, Suzanne, Tison, François, Vidailhet, Marie, Corvol, Jean-Christophe, Agid, Yves, Anheim, Mathieu, Bonnet, Anne-Marie, Borg, Michel, Broussolle, Emmanuel, Durif, Franck, Krack, Paul, Klebe, Stephan, Lohmann, Ebba, Vérin, Marc, Viallet, François, Brice, Alexis, Majounie, Elisa, Corvol, Jean Christophe, Ben-Shlomo, Yoav, Berg, Daniela, Bhatia, Kailash, Bochdanovits, Zoltan, Bonin, Michael, Bras, Jose M., Brockmann, Kathrin, Burn, David J., Chen, Honglei, Clarke, Carl E., Cookson, Mark R., Counsell, Carl, van Dijk, Karin D., Dong, Jing, Escott-Price, Valentina, Evans, Jonathan R., Gray, Emma, Guerreiro, Rita, van Hilten, Jacobus J., Hollenbeck, Albert, Holmans, Peter, Hu, Michèle, Hudson, Gavin, Hunt, Sarah E., Kilarski, Laura L., Jansen, Iris E., Langford, Cordelia, Lees, Andrew, Lorenz, Delia, Lubbe, Steven, Lungu, Codrin, Martinez, María, Mätzler, Walter, McNeill, Alisdair, Moorby, Catriona, O’Sullivan, Sean S., Pearson, Justin, Ravina, Bernard, Rivadeneira, Fernando, Ryten, Mina, Schapira, Anthony, Sharma, Manu, Sheerin, Una-Marie, Sidransky, Ellen, Spencer, Chris C.A., Stefánsson, Kári, Strange, Amy, Talbot, Kevin, Trabzuni, Daniah, Uitterlinden, André G., van de Warrenburg, Bart, Williams-Gray, Caroline H., Winder-Rhodes, Sophie, Hardy, John, Wood, Nicholas W.
Published in American journal of human genetics (03.03.2016)
Published in American journal of human genetics (03.03.2016)
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The endoplasmic reticulum-mitochondria interface is perturbed in PARK2 knockout mice and patients with PARK2 mutations
Gautier, Clément A, Erpapazoglou, Zoi, Mouton-Liger, François, Muriel, Marie Paule, Cormier, Florence, Bigou, Stéphanie, Duffaure, Sophie, Girard, Mathilde, Foret, Benjamin, Iannielli, Angelo, Broccoli, Vania, Dalle, Carine, Bohl, Delphine, Michel, Patrick P, Corvol, Jean-Christophe, Brice, Alexis, Corti, Olga
Published in Human molecular genetics (15.07.2016)
Published in Human molecular genetics (15.07.2016)
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Biochemical analysis of Parkinson's disease-causing variants of Parkin, an E3 ubiquitin–protein ligase with monoubiquitylation capacity
Hampe, Cornelia, Ardila-Osorio, Hector, Fournier, Margot, Brice, Alexis, Corti, Olga
Published in Human molecular genetics (01.07.2006)
Published in Human molecular genetics (01.07.2006)
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Transcriptional repression of p53 by parkin and impairment by mutations associated with autosomal recessive juvenile Parkinson's disease
Safe, Stephen, Abou-Sleiman, Patrick M, Wood, Nicholas W, Shen, Jie, Sunyach, Claire, West, Andrew, Giaime, Emilie, Takahashi, Hitoshi, Checler, Frédéric, Brice, Alexis, da Costa, Cristine Alves, Corti, Olga, Goldberg, Mathew S
Published in Nature cell biology (01.11.2009)
Published in Nature cell biology (01.11.2009)
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Heterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25
Barbier, Mathieu, Bahlo, Melanie, Pennisi, Alessandra, Jacoupy, Maxime, Tankard, Rick M., Ewenczyk, Claire, Davies, Kayli C., Lino‐Coulon, Patricia, Colace, Claire, Rafehi, Haloom, Auger, Nicolas, Ansell, Brendan R. E., Stelt, Ivo, Howell, Katherine B., Coutelier, Marie, Amor, David J., Mundwiller, Emeline, Guillot‐Noël, Lena, Storey, Elsdon, Gardner, R. J. McKinlay, Wallis, Mathew J., Brusco, Alfredo, Corti, Olga, Rötig, Agnès, Leventer, Richard J., Brice, Alexis, Delatycki, Martin B., Stevanin, Giovanni, Lockhart, Paul J., Durr, Alexandra
Published in Annals of neurology (01.07.2022)
Published in Annals of neurology (01.07.2022)
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P arkin deficiency modulates NLRP 3 inflammasome activation by attenuating an A 20‐dependent negative feedback loop
Mouton‐Liger, François, Rosazza, Thibault, Sepulveda‐Diaz, Julia, Ieang, Amélie, Hassoun, Sidi‐Mohamed, Claire, Emilie, Mangone, Graziella, Brice, Alexis, Michel, Patrick P., Corvol, Jean‐Christophe, Corti, Olga
Published in Glia (01.08.2018)
Published in Glia (01.08.2018)
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