MG132‐induced progerin clearance is mediated by autophagy activation and splicing regulation von Harhouri, Karim, Navarro, Claire, Depetris, Danielle, Mattei, Marie‐Geneviève, Nissan, Xavier, Cau, Pierre, De Sandre‐Giovannoli, Annachiara, Lévy, Nicolas

Volltext

Low lamin A expression in lung adenocarcinoma cells from pleural effusions is a pejorative factor associated with high number of metastatic sites and poor Performance status von Kaspi, Elise, Frankel, Diane, Guinde, Julien, Perrin, Sophie, Laroumagne, Sophie, Robaglia-Schlupp, Andrée, Ostacolo, Kevin, Harhouri, Karim, Tazi-Mezalek, Rachid, Micallef, Joelle, Dutau, Hervé, Tomasini, Pascale, De Sandre-Giovannoli, Annachiara, Lévy, Nicolas, Cau, Pierre, Astoul, Philippe, Roll, Patrice

Volltext

Progeria, a model for accelerated aging exhibited by HIV patients? von Cau, Pierre

Volltext

Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy von Navarro, Claire L., De Sandre-Giovannoli, Annachiara, Bernard, Rafaëlle, Boccaccio, Irène, Boyer, Amandine, Geneviève, David, Hadj-Rabia, Smail, Gaudy-Marqueste, Caroline, Smitt, Henk Sillevis, Vabres, Pierre, Faivre, Laurence, Verloes, Alain, Van Essen, Ton, Flori, Elisabeth, Hennekam, Raoul, Beemer, Frits A., Laurent, Nicole, Le Merrer, Martine, Cau, Pierre, Lévy, Nicolas

Volltext

Identification of CD146 as a novel molecular actor involved in systemic sclerosis von Kaspi, Elise, PharmD, PhD, Heim, Xavier, Granel, Brigitte, MD, PhD, Guillet, Benjamin, PharmD, PhD, Stalin, Jimmy, PhD, Nollet, Marie, Bertaud-Foucault, Alexandrine, PhD, Robaglia-Schlupp, Andrée, MD, Roll, Patrice, MD, PhD, Cau, Pierre, MD, PhD, Leroyer, Aurélie, PhD, Bachelier, Richard, PhD, Benyamine, Audrey, MD, PhD, Dignat-George, Françoise, PharmD, PhD, Blot-Chabaud, Marcel, PhD, Bardin, Nathalie, PharmD, PhD

Volltext

Loss of ZMPSTE24 (FACE-1) causes autosomal recessive restrictive dermopathy and accumulation of Lamin A precursors von Navarro, Claire L., Cadiñanos, Juan, Sandre-Giovannoli, Annachiara De, Bernard, Rafaëlle, Courrier, Sébastien, Boccaccio, Irène, Boyer, Amandine, Kleijer, Wim J., Wagner, Anja, Giuliano, Fabienne, Beemer, Frits A., Freije, Jose M., Cau, Pierre, Hennekam, Raoul C.M., López-Otín, Carlos, Badens, Catherine, Lévy, Nicolas

Volltext

MG132 Induces Progerin Clearance and Improves Disease Phenotypes in HGPS-like Patients' Cells von Harhouri, Karim, Cau, Pierre, Casey, Frank, Guedenon, Koffi Mawuse, Doubaj, Yassamine, Van Maldergem, Lionel, Mejia-Baltodano, Gerardo, Bartoli, Catherine, De Sandre-Giovannoli, Annachiara, Lévy, Nicolas

Volltext

HGPS and related premature aging disorders: From genomic identification to the first therapeutic approaches von Pereira, Sandrine, Bourgeois, Patrice, Navarro, Claire, Esteves-Vieira, Vera, Cau, Pierre, De Sandre-Giovannoli, Annachiara, Lévy, Nicolas

Volltext

Random walk with restart on multiplex and heterogeneous biological networks von Valdeolivas, Alberto, Tichit, Laurent, Navarro, Claire, Perrin, Sophie, Odelin, Gaëlle, Levy, Nicolas, Cau, Pierre, Remy, Elisabeth, Baudot, Anaïs

Volltext

HIV-1 infection and first line ART induced differential responses in mitochondria from blood lymphocytes and monocytes: the ANRS EP45 "Aging" study von Perrin, Sophie, Cremer, Jonathan, Roll, Patrice, Faucher, Olivia, Ménard, Amélie, Reynes, Jacques, Dellamonica, Pierre, Naqvi, Alissa, Micallef, Joëlle, Jouve, Elisabeth, Tamalet, Catherine, Solas, Caroline, Pissier, Christel, Arnoux, Isabelle, Nicolino-Brunet, Corine, Espinosa, Léon, Lévy, Nicolas, Kaspi, Elise, Robaglia-Schlupp, Andrée, Poizot-Martin, Isabelle, Cau, Pierre

Volltext

HIV protease inhibitors do not cause the accumulation of prelamin A in PBMCs from patients receiving first line therapy: the ANRS EP45 "aging" study von Perrin, Sophie, Cremer, Jonathan, Faucher, Olivia, Reynes, Jacques, Dellamonica, Pierre, Micallef, Joëlle, Solas, Caroline, Lacarelle, Bruno, Stretti, Charlotte, Kaspi, Elise, Robaglia-Schlupp, Andrée, Nicolino-Brunet, Corinne, Tamalet, Corine Nicolino-Brunet Catherine, Tamalet, Catherine, Lévy, Nicolas, Poizot-Martin, Isabelle, Cau, Pierre, Roll, Patrice

Volltext

The human necdin gene, NDN , is maternally imprinted and located in the Prader-Willi syndrome chromosomal region von Bergé Lefranc, Jean-Louis, Mattel, Marie-Geneviève, Malzac, Perrine, Jay, Philippe, Cau, Pierre, Berta, Philippe, Taviaux, Sylvie, Lalande, Marc, Rougeulle, Claire, Massacrier, Annick, Moncla, Anne, Roëckel, Nathalie, Muscatelli, Françoise

Volltext

Impact of cART on CD8+T cell senescence: the ANRS EP45-aging study von Zaegel-Faucher, Olivia, Nicolino-Brunet, Corinne, Jouve, Elisabeth, Reynes, Jacques, Dellamonica, Pierre, Truillet, Romain, Solas, Caroline, Tamalet, Catherine, Cau, Pierre, Poizot-Martin, Isabelle

Volltext

Molecular evolution of the human SRPX2 gene that causes brain disorders of the Rolandic and Sylvian speech areas von Royer, Barbara, Soares, Dinesh C, Barlow, Paul N, Bontrop, Ronald E, Roll, Patrice, Robaglia-Schlupp, Andrée, Blancher, Antoine, Levasseur, Anthony, Cau, Pierre, Pontarotti, Pierre, Szepetowski, Pierre

Volltext

Complete Loss of the Cytoplasmic Carboxyl Terminus of the KCNQ2 Potassium Channel: A Novel Mutation in a Large Czech Pedigree with Benign Neonatal Convulsions or Other Epileptic Ph... von Pereira, Sandrine, Roll, Patrice, Krizova, Jitka, Genton, Pierre, Brazdil, Milan, Kuba, Robert, Cau, Pierre, Rektor, Ivan, Szepetowski, Pierre

Volltext

Combined treatment with statins and aminobisphosphonates extends longevity in a mouse model of human premature aging von Varela, Ignacio, Osorio, Fernando G, Cobo, Juan, Suárez, María F, Freije, José M P, López-Otín, Carlos, Pereira, Sandrine, Cadiñanos, Juan, Ugalde, Alejandro P, de Carlos, Félix, Navarro, Claire L, Foray, Nicolas, Cau, Pierre, Lévy, Nicolas

Volltext

Lamin a Truncation in Hutchinson-Gilford Progeria von De Sandre-Giovannoli, Annachiara, Bernard, Rafaëlle, Cau, Pierre, Navarro, Claire, Amiel, Jeanne, Boccaccio, Irène, Lyonnet, Stanislas, Stewart, Colin L., Munnich, Arnold, Le Merrer, Martine, Lévy, Nicolas

Volltext

Molecular bases of progeroid syndromes von Navarro, Claire L., Cau, Pierre, Lévy, Nicolas

Volltext

Nuclear matrix, nuclear envelope and premature aging syndromes in a translational research perspective von Cau, Pierre, Navarro, Claire, Harhouri, Karim, Roll, Patrice, Sigaudy, Sabine, Kaspi, Elise, Perrin, Sophie, De Sandre-Giovannoli, Annachiara, Lévy, Nicolas

Volltext

Mutations in BCAP31 Cause a Severe X-Linked Phenotype with Deafness, Dystonia, and Central Hypomyelination and Disorganize the Golgi Apparatus von Cacciagli, Pierre, Sutera-Sardo, Julie, Borges-Correia, Ana, Roux, Jean-Christophe, Dorboz, Imen, Desvignes, Jean-Pierre, Badens, Catherine, Delepine, Marc, Lathrop, Mark, Cau, Pierre, Lévy, Nicolas, Girard, Nadine, Sarda, Pierre, Boespflug-Tanguy, Odile, Villard, Laurent

Volltext