Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Andrée Robaglia-Schlupp"'
Autor:
Elise Kaspi, Diane Frankel, Julien Guinde, Sophie Perrin, Sophie Laroumagne, Andrée Robaglia-Schlupp, Kevin Ostacolo, Karim Harhouri, Rachid Tazi-Mezalek, Joelle Micallef, Hervé Dutau, Pascale Tomasini, Annachiara De Sandre-Giovannoli, Nicolas Lévy, Pierre Cau, Philippe Astoul, Patrice Roll
Publikováno v:
PLoS ONE, Vol 12, Iss 8, p e0183136 (2017)
The type V intermediate filament lamins are the principal components of the nuclear matrix, including the nuclear lamina. Lamins are divided into A-type and B-type, which are encoded by three genes, LMNA, LMNB1, and LMNB2. The alternative splicing of
Externí odkaz:
https://doaj.org/article/74b656504dfd40b5abb9c1966b701d0e
Autor:
Donatienne Bourlard, Diane Frankel, Emel Peker, Patrice Roll, Stéphane Garcia, Adèle Groliere, Elise Kaspi, Andrée Robaglia-Schlupp
Publikováno v:
Annales de Pathologie. 39:227-236
The identification of ALK and ROS1 rearrangements has become essential for the theranostic management of patients with non-small cell lung cancer, especially in stage IV or inoperable patients. These testings are now performed by immunohistochemistry
Autor:
Sophie Perrin, Jonathan Cremer, Olivia Faucher, Jacques Reynes, Pierre Dellamonica, Joëlle Micallef, Caroline Solas, Bruno Lacarelle, Charlotte Stretti, Elise Kaspi, Andrée Robaglia-Schlupp, Corine Nicolino-Brunet, Catherine Tamalet, Nicolas Lévy, Isabelle Poizot-Martin, Pierre Cau, Patrice Roll
Publikováno v:
PLoS ONE, Vol 8, Iss 8 (2013)
Externí odkaz:
https://doaj.org/article/a2440acefe4e49cd8ff0be82d2afb419
Autor:
Ola Hadadeh, Emilie Barruet, Franck Peiretti, Monique Verdier, Denis Bernot, Yasmine Hadjal, Claire El Yazidi, Andrée Robaglia-Schlupp, Andre Maues De Paula, Didier Nègre, Michelina Iacovino, Michael Kyba, Marie-Christine Alessi, Bernard Binétruy
Publikováno v:
PLoS ONE, Vol 7, Iss 11, p e49065 (2012)
Regulation of the extracellular matrix (ECM) plays an important functional role either in physiological or pathological conditions. The plasminogen activation (PA) system, comprising the uPA and tPA proteases and their inhibitor PAI-1, is one of the
Externí odkaz:
https://doaj.org/article/1e5f7d84cb734b4dba74ed68d267a65e
Autor:
Sophie Perrin, Jonathan Cremer, Patrice Roll, Olivia Faucher, Amélie Ménard, Jacques Reynes, Pierre Dellamonica, Alissa Naqvi, Joëlle Micallef, Elisabeth Jouve, Catherine Tamalet, Caroline Solas, Christel Pissier, Isabelle Arnoux, Corine Nicolino-Brunet, Léon Espinosa, Nicolas Lévy, Elise Kaspi, Andrée Robaglia-Schlupp, Isabelle Poizot-Martin, Pierre Cau
Publikováno v:
PLoS ONE, Vol 7, Iss 7, p e41129 (2012)
The ANRS EP45 "Aging" study investigates the cellular mechanisms involved in the accelerated aging of HIV-1 infected and treated patients. The data reported focus on mitochondria, organelles known to be involved in cell senescence.49 HIV-1 infected p
Externí odkaz:
https://doaj.org/article/97b55a40e0714b9e9dd9845210e6f4f2
Autor:
Sophie Perrin, Jonathan Cremer, Olivia Faucher, Jacques Reynes, Pierre Dellamonica, Joëlle Micallef, Caroline Solas, Bruno Lacarelle, Charlotte Stretti, Elise Kaspi, Andrée Robaglia-Schlupp, Corinne Nicolino-Brunet, Catherine Tamalet, Nicolas Lévy, Isabelle Poizot-Martin, Pierre Cau, Patrice Roll
Publikováno v:
PLoS ONE, Vol 7, Iss 12, p e53035 (2012)
The ANRS EP45 "Aging" study investigates the cellular mechanisms involved in the accelerated aging of HIV-1 infected and treated patients. The present report focuses on lamin A processing, a pathway known to be altered in systemic genetic progeroid s
Externí odkaz:
https://doaj.org/article/f10f2f65b8fd4eda9018332af527c623
Autor:
Patrice Roll, Damien Sanlaville, Jennifer Cillario, Audrey Labalme, Nadine Bruneau, Annick Massacrier, Marc Délepine, Philippe Dessen, Vladimir Lazar, Andrée Robaglia-Schlupp, Gaëtan Lesca, Elisabeth Jouve, Gabrielle Rudolf, Jacques Rochette, G Mark Lathrop, Pierre Szepetowski
Publikováno v:
PLoS ONE, Vol 5, Iss 10, p e13750 (2010)
BACKGROUND: Benign infantile convulsions and paroxysmal dyskinesia are episodic cerebral disorders that can share common genetic bases. They can be co-inherited as one single autosomal dominant trait (ICCA syndrome); the disease ICCA gene maps at chr
Externí odkaz:
https://doaj.org/article/1a1a4866687d406094e2e237a8390462
Autor:
Diane, Frankel, Donatienne, Bourlard, Stéphane, Garcia, Andrée, Robaglia-Schlupp, Emel, Peker, Adèle, Groliere, Elise, Kaspi, Patrice, Roll
Publikováno v:
Annales de pathologie. 39(3)
The identification of ALK and ROS1 rearrangements has become essential for the theranostic management of patients with non-small cell lung cancer, especially in stage IV or inoperable patients. These testings are now performed by immunohistochemistry
Autor:
Julien Guinde, Isabelle Nanni-Metellus, Diane Frankel, Philippe Astoul, Elise Kaspi, L'Houcine Ouafik, Pascale Tomasini, Florent Amatore, Véronique Secq, Andrée Robaglia-Schlupp, Patrice Roll, Fabrice Barlesi
Publikováno v:
Clinical Chemistry and Laboratory Medicine
Clinical Chemistry and Laboratory Medicine, De Gruyter, 2018, 56 (5), pp.748-753. ⟨10.1515/cclm-2017-0527⟩
Clinical Chemistry and Laboratory Medicine, De Gruyter, 2018, 56 (5), pp.748-753. ⟨10.1515/cclm-2017-0527⟩
Background:In lung adenocarcinoma, molecular profiling of actionable genes has become essential to set up targeted therapies. However, the feasibility and the relevance of molecular profiling from the cerebrospinal fluid (CSF) in the context of menin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db447de9cb30b38322dee2116496bcc7
https://hal-amu.archives-ouvertes.fr/hal-01769686
https://hal-amu.archives-ouvertes.fr/hal-01769686
Autor:
Martha Spilioti, Eva Morava, Claire Navarro, Nathalie Da Silva, Marc Bartoli, Athanasios Evangeliou, Martine Lemerrer, Sabine Sigaudy, Kyriaki Papadopoulou-Legbelou, Racha Fayek, Patrice Roll, Andrée Robaglia-Schlupp, Florian Barthélémy, Nicolas Lévy, Annachiara De Sandre-Giovannoli, Ron A. Wevers, Gisèle Bonne, Junko Oshima
Publikováno v:
European Journal of Human Genetics
European Journal of Human Genetics, Nature Publishing Group, 2015, 23 (8), pp.1051-1061. ⟨10.1038/ejhg.2014.239⟩
European Journal of Human Genetics, 23, 8, pp. 1051-61
European Journal of Human Genetics, 2015, 23 (8), pp.1051-1061. ⟨10.1038/ejhg.2014.239⟩
European Journal of Human Genetics, 23, 1051-61
European Journal of Human Genetics, Nature Publishing Group, 2015, 23 (8), pp.1051-1061. ⟨10.1038/ejhg.2014.239⟩
European Journal of Human Genetics, 23, 8, pp. 1051-61
European Journal of Human Genetics, 2015, 23 (8), pp.1051-1061. ⟨10.1038/ejhg.2014.239⟩
European Journal of Human Genetics, 23, 1051-61
Contains fulltext : 154354.pdf (Publisher’s version ) (Closed access) Premature aging syndromes are rare genetic disorders mimicking clinical and molecular features of aging. A recently identified group of premature aging syndromes is linked to mut