Zobrazeno 1 - 10
of 134
pro vyhledávání: '"Isabelle, Baró"'
Publikováno v:
Frontiers in Physiology, Vol 15 (2024)
Externí odkaz:
https://doaj.org/article/b229578ad94c48459c74f65184d9a5fc
Autor:
Barbara B. R. Oliveira‐Mendes, Malak Alameh, Jérôme Montnach, Béatrice Ollivier, Solène Gibaud, Sylvain Feliciangeli, Florian Lesage, Flavien Charpentier, Gildas Loussouarn, Michel De Waard, Isabelle Baró
Publikováno v:
Clinical and Translational Medicine, Vol 13, Iss 5, Pp n/a-n/a (2023)
Externí odkaz:
https://doaj.org/article/40978472905f4000b05d8795faddb34a
Autor:
Barbara B. R. Oliveira-Mendes, Malak Alameh, Béatrice Ollivier, Jérôme Montnach, Nicolas Bidère, Frédérique Souazé, Nicolas Escriou, Flavien Charpentier, Isabelle Baró, Michel De Waard, Gildas Loussouarn
Publikováno v:
Cells, Vol 12, Iss 11, p 1474 (2023)
Controversial reports have suggested that SARS-CoV E and 3a proteins are plasma membrane viroporins. Here, we aimed at better characterizing the cellular responses induced by these proteins. First, we show that expression of SARS-CoV-2 E or 3a protei
Externí odkaz:
https://doaj.org/article/633e57adb491400ea4f4c0e3ef2f4bb4
Autor:
Jérôme Montnach, Maxime Lorenzini, Adrien Lesage, Isabelle Simon, Sébastien Nicolas, Eléonore Moreau, Céline Marionneau, Isabelle Baró, Michel De Waard, Gildas Loussouarn
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-16 (2021)
Abstract The patch-clamp technique and more recently the high throughput patch-clamp technique have contributed to major advances in the characterization of ion channels. However, the whole-cell voltage-clamp technique presents certain limits that ne
Externí odkaz:
https://doaj.org/article/fc995879801249e6af526213e9a3435d
Autor:
Barbara Oliveira‐Mendes, Sylvain Feliciangeli, Mélissa Ménard, Frank Chatelain, Malak Alameh, Jérôme Montnach, Sébastien Nicolas, Béatrice Ollivier, Julien Barc, Isabelle Baró, Jean‐Jacques Schott, Vincent Probst, Florence Kyndt, Isabelle Denjoy, Florian Lesage, Gildas Loussouarn, Michel De Waard
Publikováno v:
Clinical and Translational Medicine, Vol 11, Iss 11, Pp n/a-n/a (2021)
Abstract Background and aims Mutations in KCNH2 cause long or short QT syndromes (LQTS or SQTS) predisposing to life‐threatening arrhythmias. Over 1000 hERG variants have been described by clinicians, but most remain to be characterised. The object
Externí odkaz:
https://doaj.org/article/acbf1713166b446c8093329363ed25ac
Autor:
Zeina R. Al Sayed, Mariam Jouni, Jean‐Baptiste Gourraud, Nadjet Belbachir, Julien Barc, Aurore Girardeau, Virginie Forest, Aude Derevier, Anne Gaignerie, Caroline Chariau, Bastien Cimarosti, Robin Canac, Pierre Olchesqui, Eric Charpentier, Jean‐Jacques Schott, Richard Redon, Isabelle Baró, Vincent Probst, Flavien Charpentier, Gildas Loussouarn, Kazem Zibara, Guillaume Lamirault, Patricia Lemarchand, Nathalie Gaborit
Publikováno v:
Clinical and Translational Medicine, Vol 11, Iss 6, Pp n/a-n/a (2021)
Externí odkaz:
https://doaj.org/article/2317e090f55f4c2ab06747c2064a68e2
Publikováno v:
Europace
Aims Coronavirus disease of 2019 (COVID-19) has rapidly become a worldwide pandemic. Many clinical trials have been initiated to fight the disease. Among those, hydroxychloroquine and azithromycin had initially been suggested to improve clinical outc
Autor:
Vincent Portero, Solena Le Scouarnec, Zeineb Es‐Salah‐Lamoureux, Sophie Burel, Jean‐Baptiste Gourraud, Stéphanie Bonnaud, Pierre Lindenbaum, Floriane Simonet, Jade Violleau, Estelle Baron, Eléonore Moreau, Carol Scott, Stéphanie Chatel, Gildas Loussouarn, Thomas O'Hara, Philippe Mabo, Christian Dina, Hervé Le Marec, Jean‐Jacques Schott, Vincent Probst, Isabelle Baró, Céline Marionneau, Flavien Charpentier, Richard Redon
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 5, Iss 6 (2016)
BackgroundThe Brugada syndrome is an inherited cardiac arrhythmia associated with high risk of sudden death. Although 20% of patients with Brugada syndrome carry mutations in SCN5A, the molecular mechanisms underlying this condition are still largely
Externí odkaz:
https://doaj.org/article/b67e2535b2574e7c940289a9f00f97ea
Autor:
Vicki Athanasopoulos, Todor Arsov, Matthew C. Cook, Sui Rong Wayne Chen, Peter J. Schwartz, Ruiwu Wang, Deborah DiSilvestre, Hariharan Raju, David A Wallace, Richard Redon, Marcin Adamski, Helene Halkjær Jensen, Ivy E. Dick, Antony Kaspi, Melanie Bahlo, Matthew A. Field, Jinhong Wei, Lia Crotti, Michael Toft Overgaard, Mette Nyegaard, Haloom Rafehi, Bárbara B Ribeiro de Oliveira-Mendes, Carola G. Vinuesa, Yafei Zhang, Flavien Charpentier, Isabelle Baró, Malene Brohus
Publikováno v:
Europace
Brohus, M, Arsov, T, Wallace, D A, Jensen, H H, Nyegaard, M, Crotti, L, Adamski, M, Zhang, Y, Field, M A, Athanasopoulos, V, Baró, I, Ribeiro de Oliveira-Mendes, B B, Redon, R, Charpentier, F, Raju, H, DiSilvestre, D, Wei, J, Wang, R, Rafehi, H, Kaspi, A, Bahlo, M, Dick, I E, Chen, S R W, Cook, M C, Vinuesa, C G, Overgaard, M T & Schwartz, P J 2021, ' Infanticide vs. inherited cardiac arrhythmias ', Europace, vol. 23, no. 3, pp. 441-450 . https://doi.org/10.1093/europace/euaa272
EP-Europace
EP-Europace, Oxford University Press (OUP): Policy B, 2020, ⟨10.1093/europace/euaa272⟩
Brohus, M, Arsov, T, Wallace, D A, Jensen, H H, Nyegaard, M, Crotti, L, Adamski, M, Zhang, Y, Field, M A, Athanasopoulos, V, Baró, I, Ribeiro de Oliveira-Mendes, B B, Redon, R, Charpentier, F, Raju, H, DiSilvestre, D, Wei, J, Wang, R, Rafehi, H, Kaspi, A, Bahlo, M, Dick, I E, Chen, S R W, Cook, M C, Vinuesa, C G, Overgaard, M T & Schwartz, P J 2021, ' Infanticide vs. inherited cardiac arrhythmias ', Europace, vol. 23, no. 3, pp. 441-450 . https://doi.org/10.1093/europace/euaa272
EP-Europace
EP-Europace, Oxford University Press (OUP): Policy B, 2020, ⟨10.1093/europace/euaa272⟩
Aims In 2003, an Australian woman was convicted by a jury of smothering and killing her four children over a 10-year period. Each child died suddenly and unexpectedly during a sleep period, at ages ranging from 19 days to 18 months. In 2019 we were a
Autor:
Julien Barc, Béatrice Ollivier, Sylvain Feliciangeli, Malak Alameh, Vincent Probst, Isabelle Denjoy, Barbara Oliveira-Mendes, Jean-Jacques Schott, Frank Chatelain, S. Nicolas, Florian Lesage, Jérôme Montnach, Isabelle Baró, Michel De Waard, F. Kyndt, Mélissa Ménard, Gildas Loussouarn
Publikováno v:
Clinical and Translational Medicine, Vol 11, Iss 11, Pp n/a-n/a (2021)
Clinical and Translational Medicine
Clinical and Translational Medicine, 2021, 11 (11), pp.100355. ⟨10.1002/ctm2.609⟩
Clinical and Translational Medicine, 2021, 11 (11), ⟨10.1002/ctm2.609⟩
Clinical and Translational Medicine
Clinical and Translational Medicine, 2021, 11 (11), pp.100355. ⟨10.1002/ctm2.609⟩
Clinical and Translational Medicine, 2021, 11 (11), ⟨10.1002/ctm2.609⟩
Background and aims Mutations in KCNH2 cause long or short QT syndromes (LQTS or SQTS) predisposing to life‐threatening arrhythmias. Over 1000 hERG variants have been described by clinicians, but most remain to be characterised. The objective is to