Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Livia, Delpiano"'
Autor:
Michael William Mather, Bernard Verdon, Rachel Anne Botting, Justin Engelbert, Livia Delpiano, Xin Xu, Catherine Hatton, Tracey Davey, Steven Lisgo, Philip Yates, Nicholas Dawe, Colin D. Bingle, Muzlifah Haniffa, Jason Powell, Chris Ward
Publikováno v:
Laryngoscope Investigative Otolaryngology, Vol 6, Iss 5, Pp 1167-1174 (2021)
Abstract Introduction Otitis media is an umbrella term for middle ear inflammation; ranging from acute infection to chronic mucosal disease. It is a leading cause of antimicrobial therapy prescriptions and surgery in children. Despite this, treatment
Externí odkaz:
https://doaj.org/article/eedd5c1112b44d41b04eeb3fcdf4bffe
Autor:
Vinciane Saint-Criq, Anita Guequén, Amber R Philp, Sandra Villanueva, Tábata Apablaza, Ignacio Fernández-Moncada, Agustín Mansilla, Livia Delpiano, Iván Ruminot, Cristian Carrasco, Michael A Gray, Carlos A Flores
Publikováno v:
eLife, Vol 11 (2022)
Bicarbonate secretion is a fundamental process involved in maintaining acid-base homeostasis. Disruption of bicarbonate entry into airway lumen, as has been observed in cystic fibrosis, produces several defects in lung function due to thick mucus acc
Externí odkaz:
https://doaj.org/article/7fa1d4fa985c414587cb3cfa40c6aee9
Publikováno v:
Biology, Vol 10, Iss 4, p 278 (2021)
Cystic fibrosis (CF) is a genetic disease associated with the defective function of the cystic fibrosis transmembrane conductance regulator (CFTR) protein that causes obstructive disease and chronic bacterial infections in airway epithelia. Deletion
Externí odkaz:
https://doaj.org/article/246969da200545a1bbee802feaa0be8c
Autor:
Vinciane Saint-Criq, Livia Delpiano, John Casement, Jennifer C. Onuora, JinHeng Lin, Michael A. Gray
Publikováno v:
Cells, Vol 9, Iss 9, p 2137 (2020)
In vitro cultures of primary human airway epithelial cells (hAECs) grown at air–liquid interface have become a valuable tool to study airway biology under normal and pathologic conditions, and for drug discovery in lung diseases such as cystic fibr
Externí odkaz:
https://doaj.org/article/9c281aa14b8e45eeb9578b34bac254eb
Autor:
Livia Delpiano, Joseph J. Thomas, Annabel R. Yates, Sarah J. Rice, Michael A. Gray, Vinciane Saint-Criq
Publikováno v:
Frontiers in Pharmacology, Vol 9 (2018)
Respiratory failure, driven by airways mucus obstruction, chronic inflammation and bacterial infections, is the main cause of mortality and morbidity in people with cystic fibrosis (CF) due to defects in the Cl- and HCO3− transport activity of the
Externí odkaz:
https://doaj.org/article/f0779eab07c24064a89c4946b6cee0a3
Publikováno v:
Frontiers in Pharmacology, Vol 9 (2018)
Cystic fibrosis (CF) is a chronic disease caused by mutations in the CF transmembrane conductance regulator (CFTR) gene, which encodes for a channel expressed at the apical surface of epithelial tissues. Defective chloride and bicarbonate secretion,
Externí odkaz:
https://doaj.org/article/4f2d866368ce419584224b862b32c3b0
Autor:
Sungwoo Jo, Raquel Centeio, Jinhong Park, Jiraporn Ousingsawat, Dong‐kyu Jeon, Khaoula Talbi, Rainer Schreiber, Kunhi Ryu, Kristin Kahlenberg, Veronika Somoza, Livia Delpiano, Michael A. Gray, Margarida D. Amaral, Violeta Railean, Jeffrey M. Beekman, Lisa W. Rodenburg, Wan Namkung, Karl Kunzelmann
Publikováno v:
The FASEB Journal. 36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84df78702cc97c0ab313559f457294ee
https://doi.org/10.1096/fj.202200313rr
https://doi.org/10.1096/fj.202200313rr
Autor:
Lisa W. Rodenburg, Livia Delpiano, Violeta Railean, Raquel Centeio, Madalena C. Pinto, Shannon M. A. Smits, Isabelle S. van der Windt, Casper F. J. van Hugten, Sam F. B. van Beuningen, Remco N. P. Rodenburg, Cornelis K. van der Ent, Margarida D. Amaral, Karl Kunzelmann, Michael A. Gray, Jeffrey M. Beekman, Gimano D. Amatngalim
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 20; Pages: 12657
Individuals with Cystic Fibrosis (CF) suffer from severe respiratory disease due to a genetic defect in the Cystic Fibrosis Transmembrane conductance Regulator (CFTR) gene, which impairs airway epithelial ion and fluid secretion. New CFTR modulators
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77607e7be56cda9c2ffed67cfddca9fb
https://doi.org/10.1101/2022.09.23.509034
https://doi.org/10.1101/2022.09.23.509034
Autor:
Sungwoo, Jo, Raquel, Centeio, Jinhong, Park, Jiraporn, Ousingsawat, Dong-Kyu, Jeon, Khaoula, Talbi, Rainer, Schreiber, Kunhi, Ryu, Kristin, Kahlenberg, Veronika, Somoza, Livia, Delpiano, Michael A, Gray, Margarida D, Amaral, Violeta, Railean, Jeffrey M, Beekman, Lisa W, Rodenburg, Wan, Namkung, Karl, Kunzelmann
Publikováno v:
FASEB journal : official publication of the Federation of American Societies for Experimental BiologyREFERENCES. 36(11)
The solute carrier 26 family member A9 (SLC26A9) is an epithelial anion transporter that is assumed to contribute to airway chloride secretion and surface hydration. Whether SLC26A9 or CFTR is responsible for airway Cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c3cea7d2fcdf1a23111e7c3069f6e1a5
https://pubmed.ncbi.nlm.nih.gov/36183361
https://pubmed.ncbi.nlm.nih.gov/36183361
Autor:
Vinciane Saint-Criq, Anita Guequén, Amber R Philp, Sandra Villanueva, Tábata Apablaza, Ignacio Fernández-Moncada, Agustín Mansilla, Livia Delpiano, Iván Ruminot, Cristian Carrasco, Michael A Gray, Carlos A Flores
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aecf8d97fa6028753b6c57c3f7927b62
https://doi.org/10.7554/elife.75871.sa2
https://doi.org/10.7554/elife.75871.sa2