Zobrazeno 1 - 10
of 841
pro vyhledávání: '"Fajac A"'
Publikováno v:
European Respiratory Review, Vol 33, Iss 173 (2024)
Cystic fibrosis (CF) is a genetic disease caused by variants in the gene encoding for the CF transmembrane conductance regulator (CFTR) protein, a chloride and bicarbonate channel. CFTR dysfunction results in a multiorgan disease with the main clinic
Externí odkaz:
https://doaj.org/article/e65d0abd705d4af2a19b1ed22205f43a
Autor:
Anne Fajac, Iva Simeonova, Julia Leemput, Marc Gabriel, Aurélie Morin, Vincent Lejour, Annaïg Hamon, Jeanne Rakotopare, Wilhelm Vaysse-Zinkhöfer, Eliana Eldawra, Marina Pinskaya, Antonin Morillon, Jean-Christophe Bourdon, Boris Bardot, Franck Toledo
Publikováno v:
eLife, Vol 13 (2024)
The Trp53 gene encodes several isoforms of elusive biological significance. Here, we show that mice lacking the Trp53 alternatively spliced (AS) exon, thereby expressing the canonical p53 protein but not isoforms with the AS C-terminus, have unexpect
Externí odkaz:
https://doaj.org/article/24d352706ace432cafb1b14b25ca0b61
Autor:
De Wachter, E, De Boeck, K, Sermet-Gaudelus, I, Simmonds, NJ, Munck, A, Naehrlich, L, Barben, J, Boyd, C, Veen, SJ, Carr, SB, Fajac, I, Farrell, PM, Girodon, E, Gonska, T, Grody, WW, Jain, M, Jung, A, Kerem, E, Raraigh, KS, van Koningsbruggen-Rietschel, S, Waller, MD, Southern, KW, Castellani, C
Publikováno v:
In Journal of Cystic Fibrosis May 2024 23(3):388-397
Autor:
Southern, Kevin W, Addy, Charlotte, Bell, Scott C, Bevan, Amanda, Borawska, Urzula, Brown, Catherine, Burgel, Pierre-Régis, Button, Brenda, Castellani, Carlo, Chansard, Audrey, Chilvers, Mark A, Davies, Gwyneth, Davies, Jane C, De Boeck, Kris, Declercq, Dimitri, Doumit, Michael, Drevinek, Pavel, Fajac, Isabelle, Gartner, Silvia, Georgiopoulos, Anna M, Gursli, Sandra, Gramegna, Andrea, Hansen, Carina ME, Hug, Martin J, Lammertyn, Elise, Landau, Edwina (Eddie) C., Langley, Ross, Mayer-Hamblett, Nicole, Middleton, Anna, Middleton, Peter G, Mielus, Monika, Morrison, Lisa, Munck, Anne, Plant, Barry, Ploeger, Maarten, Bertrand, Dominique Pougheon, Pressler, Tacjana, Quon, Bradley S, Radtke, Thomas, Saynor, Zoe L, Shufer, Ilan, Smyth, Alan R, Smith, Chris, van Koningsbruggen-Rietschel, Silke
Publikováno v:
In Journal of Cystic Fibrosis January 2024 23(1):12-28
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Hisert, Katherine B *, Birket, Susan E, Clancy, John Paul, Downey, Damian G, Engelhardt, John F, Fajac, Isabelle, Gray, Robert D, Lachowicz-Scroggins, Marrah E, Mayer-Hamblett, Nicole, Thibodeau, Patrick, Tuggle, Katherine L, Wainwright, Claire E, De Boeck, Kris
Publikováno v:
In The Lancet Respiratory Medicine October 2023 11(10):916-931
Autor:
Mayer-Hamblett, Nicole *, Clancy, John Paul, Jain, Raksha, Donaldson, Scott H, Fajac, Isabelle, Goss, Christopher H, Polineni, Deepika, Ratjen, Felix, Quon, Bradley S, Zemanick, Edith T, Bell, Scott C, Davies, Jane C, Jain, Manu, Konstan, Michael W, Kerper, Natanya R, LaRosa, Tré *, Mall, Marcus A, McKone, Edward, Pearson, Kelsie, Pilewski, Joseph M, Quittell, Lynne, Rayment, Jonathan H, Rowe, Steven M, Taylor-Cousar, Jennifer L, Retsch-Bogart, George, Downey, Damian G
Publikováno v:
In The Lancet Respiratory Medicine October 2023 11(10):932-944
Autor:
Fajac, Isabelle, Burgel, Pierre-Régis
Publikováno v:
In La Presse Médicale September 2023 52(3)
Autor:
Reinert Philippe, Bismuth Elise, Davy Nolwen, Pierrot Sébastien, Parbaille Bastien, Bidou Laure, Fajac Anne, Renouil Michel, Sermet-Gaudelus Isabelle, Lenoir Gérard, Lesure Jean, Rousset Jean, Edelman Aleksander
Publikováno v:
BMC Medicine, Vol 5, Iss 1, p 5 (2007)
Abstract Background Cystic fibrosis (CF) is caused by mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR) protein, which acts as a chloride channel activated by cyclic AMP (cAMP). The most frequent mutation f
Externí odkaz:
https://doaj.org/article/bfeb0d8a24274a1c956a4a6af5e94087
Autor:
Grenet Dominique, Fajac Anne, Cesari Danielle, Bernaudin Jean-François, Stéphan François, Caubarrere Isabelle, Stern Marc
Publikováno v:
BMC Infectious Diseases, Vol 1, Iss 1, p 15 (2001)
Abstract Background Cytomegalovirus (CMV) pneumonitis has been shown to be associated with lymphocytic alveolitis after lung transplantation. In the present study, we investigated a series of bronchoalveolar (BAL) and blood samples, collected in the
Externí odkaz:
https://doaj.org/article/b578f61071db4f369ccf5bfcddd16d66