Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Anne-Laure Egesipe"'
Autor:
Romain Ollier, Aline Fuchs, Florence Gauye, Katarzyna Piorkowska, Sébastien Menant, Monisha Ratnam, Paolo Montanari, Florence Guilhot, Didier Phillipe, Mickael Audrain, Anne-Laure Egesipe, Damien Névoltris, Tamara Seredenina, Andrea Pfeifer, Marie Kosco-Vilbois, Tariq Afroz
Publikováno v:
mAbs, Vol 15, Iss 1 (2023)
ABSTRACTOptimal pharmacokinetic (PK) properties of therapeutic monoclonal antibodies (mAbs) are essential to achieve the desired pharmacological benefits in patients. To accomplish this, we followed an approach comprising structure-based mAb charge e
Externí odkaz:
https://doaj.org/article/9a5ae63d53e7442fa5091ec231d7f99f
Autor:
Tariq Afroz, Elodie Chevalier, Mickael Audrain, Christopher Dumayne, Tamar Ziehm, Roger Moser, Anne-Laure Egesipe, Lorène Mottier, Monisha Ratnam, Manuela Neumann, Daniel Havas, Romain Ollier, Kasia Piorkowska, Mayank Chauhan, Alberto B. Silva, Samjhana Thapa, Jan Stöhr, Andrej Bavdek, Valerie Eligert, Oskar Adolfsson, Peter T. Nelson, Sílvia Porta, Virginia M.-Y. Lee, Andrea Pfeifer, Marie Kosco-Vilbois, Tamara Seredenina
Publikováno v:
Neurobiology of Disease, Vol 179, Iss , Pp 106050- (2023)
Effective therapies are urgently needed to safely target TDP-43 pathology as it is closely associated with the onset and development of devastating diseases such as frontotemporal lobar degeneration with TDP-43 pathology (FTLD-TDP) and amyotrophic la
Externí odkaz:
https://doaj.org/article/0ae8a176004d45538a54e3b880d79375
Autor:
Patricia R. Pitrez, Luís Estronca, Luís Miguel Monteiro, Guillem Colell, Helena Vazão, Deolinda Santinha, Karim Harhouri, Daniel Thornton, Claire Navarro, Anne-Laure Egesipe, Tânia Carvalho, Rodrigo L. Dos Santos, Nicolas Lévy, James C. Smith, João Pedro de Magalhães, Alessandro Ori, Andreia Bernardo, Annachiara De Sandre-Giovannoli, Xavier Nissan, Anna Rosell, Lino Ferreira
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-16 (2020)
Hutchinson-Gilford Progeria Syndrome (HGPS) is a premature aging disease and smooth muscle cells are the most affected cells in HGPS individuals. Here, the authors report a microfluidics platform with HGPS induced pluripotent stem cells and show that
Externí odkaz:
https://doaj.org/article/4ba0b6d9e607460d92755869c0269433
Autor:
Julia Hoeng, Sophie Scheuner, Stephanie Johne, Claudius Pak, Emmanuel Guedj, Athanasios Kondylis, Dariusz Peric, Fabio Maranzano, Romain Piault, Walter K. Schlage, Nikolai V. Ivanov, Thomas Schneider, Carine Poussin, Marco van der Toorn, Rebecca Savioz, Manuel C. Peitsch, Moran Morelli, Anne-Laure Egesipe, Shoaib Majeed, Remi Dulize, Celine Merg
Publikováno v:
Archives of Toxicology
Aging and smoking are major risk factors for cardiovascular diseases (CVD). Our in vitro study compared, in the context of aging, the effects of the aerosol of Tobacco Heating System 2.2 (THS; an electrically heated tobacco product) and 3R4F referenc
Autor:
Guillem Colell, Rodrigo L. dos Santos, Luís Miguel Monteiro, Andreia Bernardo, Claire Navarro, Nicolas Lévy, Lino Ferreira, Anna Rosell, Anne-Laure Egesipe, Daniel Thornton, Xavier Nissan, João Pedro de Magalhães, James C. Smith, Alessandro Ori, Karim Harhouri, Luís M.B.B. Estronca, Deolinda Santinha, Helena Vazão, Tania Rafaela Vale Carvalho, Annachiara De Sandre-Giovannoli, Patrícia R. Pitrez
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Nature Communications, Vol 11, Iss 1, Pp 1-16 (2020)
Nature Communications
Nature Communications, 2020, 11 (1), pp.4110. ⟨10.1038/s41467-020-17901-2⟩
Nature Communications, Nature Publishing Group, 2020, 11 (1), pp.4110. ⟨10.1038/s41467-020-17901-2⟩
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Nature Communications, Vol 11, Iss 1, Pp 1-16 (2020)
Nature Communications
Nature Communications, 2020, 11 (1), pp.4110. ⟨10.1038/s41467-020-17901-2⟩
Nature Communications, Nature Publishing Group, 2020, 11 (1), pp.4110. ⟨10.1038/s41467-020-17901-2⟩
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
© The Author(s) 2020. This article is licensed under a Creative Commons Attribution 4.0 International License.
Hutchinson-Gilford Progeria Syndrome (HGPS) is a premature aging disease in children that leads to early death. Smooth muscle cells (
Hutchinson-Gilford Progeria Syndrome (HGPS) is a premature aging disease in children that leads to early death. Smooth muscle cells (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf097f9d9bc35c3035baa5f8c47888aa
Autor:
Manoubia Saidani, Xavier Nissan, Annachiara De Sandre-Giovannoli, Lucile Hoch, Jennifer Allouche, Alessandra Lo Cicero, Sabine Sigaudy, Celine Bruge, Christine Baldeschi, Anne Laure Egesipe, Nicolas Lévy
Publikováno v:
Scientific Reports
Scientific Reports, Nature Publishing Group, 2018, 8 (1), ⟨10.1038/s41598-018-27165-y⟩
Scientific Reports, 2018, 8 (1), ⟨10.1038/s41598-018-27165-y⟩
Scientific Reports, Vol 8, Iss 1, Pp 1-10 (2018)
Scientific Reports, Nature Publishing Group, 2018, 8 (1), ⟨10.1038/s41598-018-27165-y⟩
Scientific Reports, 2018, 8 (1), ⟨10.1038/s41598-018-27165-y⟩
Scientific Reports, Vol 8, Iss 1, Pp 1-10 (2018)
Hutchinson-Gilford Progeria Syndrome (HGPS) is a rare genetic disorder that leads to premature aging. In this study, we used induced pluripotent stem cells to investigate the hypopigmentation phenotypes observed in patients with progeria. Accordingly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e349792942f489b29e7676ed2db4f5c
https://hal-amu.archives-ouvertes.fr/hal-01991357/file/s41598-018-27165-y.pdf
https://hal-amu.archives-ouvertes.fr/hal-01991357/file/s41598-018-27165-y.pdf
Autor:
Luís M.B.B. Estronca, Lino Ferreira, Helena Vazão, Patrícia R. Pitrez, Anne-Laure Egesipe, Claire Navarro, Nicolas Lévy, Annachiara De Sandre-Giovannoli, Amélie Le Corf, Xavier Nissan
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
ACS Biomaterials Science and Engineering
ACS Biomaterials Science and Engineering, 2018, 4 (5), pp.1498-1504
HAL
ACS Biomaterials Science & Engineering
ACS Biomaterials Science and Engineering, ACS, 2018, 4 (5), pp.1498-1504
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
ACS Biomaterials Science and Engineering
ACS Biomaterials Science and Engineering, 2018, 4 (5), pp.1498-1504
HAL
ACS Biomaterials Science & Engineering
ACS Biomaterials Science and Engineering, ACS, 2018, 4 (5), pp.1498-1504
Aging is characterized by a progressive accumulation of cellular damage, which leads to impaired function. Little is known whether substrates can influence cell aging. This is of utmost importance in the development of medical devices that are in con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::169857bdc6998ec009ed3fc9daa5c4e4
https://hdl.handle.net/10316/92391
https://hdl.handle.net/10316/92391
Autor:
Marc Peschanski, Anne-Laure Jaskowiak, Nicolas Lévy, Anne-Laure Egesipe, Sophie Blondel, Xavier Nissan, Alessandra Lo Cicero, Annachiara De Sandre-Giovannoli, Claire Navarro
Publikováno v:
NPJ Aging and Mechanisms of Disease
Hutchinson–Gilford progeria syndrome (HGPS) is a rare genetic disorder that causes systemic accelerated aging in children. This syndrome is due to a mutation in the LMNA gene that leads to the production of a truncated and toxic form of lamin A cal
Autor:
Xavier Nissan, Anne-Laure Jaskowiak, Alessandra Lo Cicero, Anne-Laure Egesipe, Benjamin Brinon, Annachiara De Sandre-Giovannoli, Lino Ferreira, Nicolas Lévy, Johana Tournois, Patrícia R. Pitrez
Publikováno v:
Scientific Reports
Scientific Reports, Nature Publishing Group, 2016, 6, ⟨10.1038/srep34798⟩
Scientific Reports, Nature Publishing Group, 2016, 6, 〈10.1038/srep34798〉
Scientific Reports, 2016, 6, ⟨10.1038/srep34798⟩
Scientific Reports, Nature Publishing Group, 2016, 6, ⟨10.1038/srep34798⟩
Scientific Reports, Nature Publishing Group, 2016, 6, 〈10.1038/srep34798〉
Scientific Reports, 2016, 6, ⟨10.1038/srep34798⟩
Hutchinson-Gilford progeria syndrome (HGPS) is a rare fatal genetic disorder that causes systemic accelerated aging in children. Thanks to the pluripotency and self-renewal properties of induced pluripotent stem cells (iPSC), HGPS iPSC-based modeling
Autor:
Patrícia R. Pitrez, Anne-Laure Jaskowiak, G. Bollot, Benjamin Brinon, C. Bauvais, Paola Picardi, A. Mejat, Johana Tournois, Maurizio Bifulco, Anne-Laure Egesipe, Lino Ferreira, A. Le Corf, J. Ragot, Marc Peschanski, Sophie Blondel, A. De Sandre-Giovannoli, P. Poydenot, P. Georges, D. Laustriat, Claire Navarro, Xavier Nissan, M. Notarnicola, Nicolas Lévy
Publikováno v:
Cell Death and Disease
Cell Death and Disease, 2016, 7, pp.e2105. ⟨10.1038/cddis.2015.374⟩
Cell Death and Disease, Nature Publishing Group, 2016, 7, pp.e2105. ⟨10.1038/cddis.2015.374⟩
Cell Death & Disease
Cell Death and Disease, 2016, 7, pp.e2105. ⟨10.1038/cddis.2015.374⟩
Cell Death and Disease, Nature Publishing Group, 2016, 7, pp.e2105. ⟨10.1038/cddis.2015.374⟩
Cell Death & Disease
Hutchinson-Gilford progeria syndrome (HGPS) is a rare genetic disorder characterized by a dramatic appearance of premature aging. HGPS is due to a single-base substitution in exon 11 of the LMNA gene (c.1824C>T) leading to the production of a toxic f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bac0ba91df2499ec3467ec122ff71b27
https://hal.science/hal-01469712/file/cddis2015374a.pdf
https://hal.science/hal-01469712/file/cddis2015374a.pdf