Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Baroukhmaurice Assael"'
Autor:
Sara Caldrer, Genny Verzè, Baroukhmaurice Assael, Mario Rosario Buffelli, Jan Evert Johansson, Paola Melotti, Gloria Tridello, Silvia Bolognin, Claudio Sorio, G. Bellisola, Marzia Vezzalini
Publikováno v:
Cytometry Part A. 85:611-620
Leukocytes have previously been shown to express detectable levels of the protein cystic fibrosis transmembrane conductance regulator (CFTR). This study aims to evaluate the application of flow cytometric (FC) analysis to detect CFTR expression, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::669c0b6538c5e44b1cbaf9ea951278e4
https://doi.org/10.1002/cyto.a.22456
https://doi.org/10.1002/cyto.a.22456
Autor:
Baroukhmaurice Assael, Harm A.W.M. Tiddens, Elena Salonini, Sonia Volpi, Marleen Bakker, P. Kroneberg, B. Müllinger, E.M. Bakker, Wim C. J. Hop
Publikováno v:
BASE-Bielefeld Academic Search Engine
Introduction Small airway obstruction is important in the pathophysiology of cystic fibrosis (CF) lung disease. Additionally, many CF patients lose lung function in the long term as a result of respiratory tract exacerbations (RTEs). No trials have b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6748b4d90da9de2cd6fd7852f124de2
https://doi.org/10.1002/ppul.22800
https://doi.org/10.1002/ppul.22800
Autor:
H. R. De Jonge, F. Catalano, Baroukhmaurice Assael, A. Cerofolini, Angela Sandri, F. Lombardo, Claudio Sorio, Silvia Vercellone, Paola Melotti, Luca Rodella, Sara Caldrer, Mario Rosario Buffelli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a74ee34cb3291413929d746524db2ff1
http://hdl.handle.net/11562/955494
http://hdl.handle.net/11562/955494
Autor:
Claudio Sorio, Denise Peserico, Paola Melotti, E. Sorio, Jeffrey J. Wine, Baroukhmaurice Assael, Marco Tagliasacchi, Stefano Ceri, Teresinha Leal, Gabriella Bergamini
Objective Wine et al, (Plos ONE 2013 and 2014) recently published a bioassay for testing CFTR function in vivo. A ratio was computed between CFTR-independent (M-sweat, stimulated by methacholine) and CFTR-dependent (C-sweat, evoked by a b-adrenergic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d96ec2dacb5625c803dfc5aeeb173aec
http://hdl.handle.net/11562/955493
http://hdl.handle.net/11562/955493
Autor:
Paola Melotti, Fabio Stellari, Federico Boschi, M. M. Lieò, Gino Villetti, Francesco Ruscitti, Gabriella Bergamini, Francesca Ravanetti, Giorgia D'onofrio, Baroukhmaurice Assael, Claudio Sorio, Angela Sandri
Publikováno v:
Journal of Cystic Fibrosis. 15:S56
and pulmonary disease management (ECFS; Sermet-Gaudelus et al. 2010). Results: There are currently 9 children diagnosed with CF following NBS enrolled at the paediatric CF specialized centre (14.8% of all patients), with a mean age of 11 months (rang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06faff4a3818de8abaa2bf5a2cc3039f
https://doi.org/10.1016/s1569-1993(16)30260-0
https://doi.org/10.1016/s1569-1993(16)30260-0
Autor:
Lucia Dora Notarangelo, Cinzia Mazza, Marcho Chiarini, Rita Padoan, Alessandro Plebani, C. Garlanda, Baroukhmaurice Assael, Gianfranco Savoldi, Cristiano Sabelli, Raffaele Badolato, Paola Melotti, Alberto Mantovani
Publikováno v:
Genes and Immunity
Genes and Immunity; Vol 11
Genes and Immunity; Vol 11
Cystic fibrosis (CF) is a common life-threatening autosomal recessive disorder in the Caucasian population, and the gene responsible is the CF transmembrane conductance regulator (CFTR). Patients with CF have repeated bacterial infection of the airwa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::213c5acf1febc9e6ecb459fdc8146723
http://hdl.handle.net/11379/47036
http://hdl.handle.net/11379/47036