Zobrazeno 1 - 10
of 98
pro vyhledávání: '"Tarze, A."'
Autor:
Mickael Shum, Charlie M. London, Maelle Briottet, Khadeeja Adam Sy, Vincent Baillif, Reginald Philippe, Abdolhossein Zare, Sadegh Ghorbani-Dalini, Natacha Remus, Agathe Tarze, Virginie Escabasse, Ralph Epaud, Marc Dubourdeau, Valerie Urbach
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Specialized pro-resolving lipid mediators (SPMs) as lipoxins (LX), resolvins (Rv), protectins (PD) and maresins (MaR) promote the resolution of inflammation. We and others previously reported reduced levels of LXA4 in bronchoalveolar lavages from cys
Externí odkaz:
https://doaj.org/article/ce8e81c55de74fc78b83a24bf45eb052
Autor:
Yamada, Elizabeth S., Respondek, Gesine, Müssner, Stefanie, de Andrade, Anderson, Höllerhage, Matthias, Depienne, Christel, Rastetter, Agnès, Tarze, Agathe, Friguet, Bertrand, Salama, Mohamed, Champy, Pierre, Oertel, Wolfgang H., Höglinger, Günter U.
Publikováno v:
In Experimental Neurology March 2014 253:113-125
Autor:
de Becdelièvre, Alix, Rocca, Jérémy, Aissat, Abdel, Drévillon, Loic, Moutereau, Stéphane, Le Gouvello, Sabine, Hinzpeter, Alexandre, Tarze, Agathe, Fanen, Pascale
Publikováno v:
In International Journal of Biochemistry and Cell Biology November 2013 45(11):2402-2409
Akademický článek
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Publikováno v:
In Journal of Biological Chemistry 26 November 2010 285(48):37324-37332
Autor:
Ralph Epaud, Pascale Fanen, Abdel Aissat, Agathe Tarze, Elodie Nattes, Stéphanie Finet, Céline Delestrain, Valérie Delattre, Stéphanie Simon, Bruno Costes, Elodie Duprat
Publikováno v:
British journal of clinical pharmacologyREFERENCES. 87(5)
Mutations in the gene encoding surfactant protein C (SP-C) cause interstitial lung disease (ILD), and glucocorticosteroid (GC) treatment is the most recognized therapy in children. We aimed to decipher the mechanisms behind successful GC treatment in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32a87f4a208cac92f57f3972e5b5b476
https://pubmed.ncbi.nlm.nih.gov/33179299
https://pubmed.ncbi.nlm.nih.gov/33179299
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Autor:
Tarze, Agathe, Dauplais, Marc, Grigoras, Ioana, Lazard, Myriam, Ha-Duong, Nguyet-Thanh, Barbier, Frédérique, Blanquet, Sylvain, Plateau, Pierre
Publikováno v:
In Journal of Biological Chemistry 23 March 2007 282(12):8759-8767
Autor:
Loïc Drévillon, Gaëlle Tanguy, Alexandre Hinzpeter, Nicole Arous, Alix de Becdelièvre, Abdel Aissat, Agathe Tarze, Michel Goossens, Pascale Fanen
Publikováno v:
PLoS ONE, Vol 6, Iss 3, p e18334 (2011)
The CFTR (cystic fibrosis transmembrane conductance regulator) protein is a large polytopic protein whose biogenesis is inefficient. To better understand the regulation of CFTR processing and trafficking, we conducted a genetic screen that identified
Externí odkaz:
https://doaj.org/article/5061d0c3eb354a89b407b3b4a012778f
Autor:
Alexandre Hinzpeter, Abdel Aissat, Elvira Sondo, Catherine Costa, Nicole Arous, Christine Gameiro, Natacha Martin, Agathe Tarze, Laurence Weiss, Alix de Becdelièvre, Bruno Costes, Michel Goossens, Luis J Galietta, Emmanuelle Girodon, Pascale Fanen
Publikováno v:
PLoS Genetics, Vol 6, Iss 10 (2010)
Approximately 30% of alleles causing genetic disorders generate premature termination codons (PTCs), which are usually associated with severe phenotypes. However, bypassing the deleterious stop codon can lead to a mild disease outcome. Splicing at NA
Externí odkaz:
https://doaj.org/article/c7ee5c74b4ae4089a975668a60796086