Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Susan Banks-Schlegel"'
Autor:
Noah Lechtzin, Nicole Mayer-Hamblett, Natalie E. West, Sarah Allgood, Ellen Wilhelm, Umer Khan, Moira L. Aitken, Bonnie W. Ramsey, Michael P. Boyle, Peter J. Mogayzel, Ronald L. Gibson, David Orenstein, Carlos Milla, John P. Clancy, Veena Antony, Christopher H. Goss, Lynne Quittell, Patrick A. Flume, Shannon S. Carson, John Conlon, Susan Banks-Schlegel, Kelli Joubran, Elena Mullin, Kathy Seidel, Dionne Howe, Scott Donaldson, Susanna McColley, John Clancy, Elliott Dasenbrook, Karen McCoy, Jerry Nick, Frank Accurso, Richard Ahrens, Joanne Billings
Individuals with cystic fibrosis (CF) experience frequent acute pulmonary exacerbations, which lead to decreased lung function and reduced quality of life.The goal of this study was to determine if an intervention directed toward early detection of p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::245ab9615356b42005eabe7bde64b36d
https://europepmc.org/articles/PMC5694835/
https://europepmc.org/articles/PMC5694835/
Autor:
Marc B. Hershenson, Reynold A. Panettieri, Susan Banks-Schlegel, Prescott G. Woodruff, Michael I. Kotlikoff, William T. Gerthoffer, Ian P. Hall
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 177:248-252
Airway smooth muscle (ASM) plays a pivotal role in modulating bronchomotor tone but also orchestrates and perpetuates airway inflammation and remodeling. Despite substantial research, there remain important unanswered questions. In 2006, the National
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88b90e801f69aecc1fae6c91aebc1e79
https://doi.org/10.1164/rccm.200708-1217pp
https://doi.org/10.1164/rccm.200708-1217pp
Publikováno v:
American Journal of Respiratory Cell and Molecular Biology. 29:642-645
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebfcfae7757c460085b5a0f5ae24cbf6
https://doi.org/10.1165/rcmb.2002-0200ws
https://doi.org/10.1165/rcmb.2002-0200ws
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 160:1035-1042
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f9b38ffa479a5d6b93779980005735e
https://doi.org/10.1164/ajrccm.160.3.9902064
https://doi.org/10.1164/ajrccm.160.3.9902064
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 156:314-319
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b6354e7fb5275cee18f3b6a152e6108
https://doi.org/10.1164/ajrccm.156.1.9612121
https://doi.org/10.1164/ajrccm.156.1.9612121
Autor:
Esther Barreiro, Susan Banks-Schlegel, Thomas L. Croxton, William E. Balch, Lisa Postow, Weiniu Gan, Scott Budinger, Ana Maria Cuervo, Daniel Finley, Richard I. Morimoto, Dorothy B. Gail, Allan M. Weissman, Jacob I. Sznajder, Ivor J. Benjamin, Aaron D. Laposky
Publikováno v:
American journal of respiratory and critical care medicine. 189(1)
Recent discoveries indicate that disorders of protein folding and degradation play a particularly important role in the development of lung diseases and their associated complications. The overarching purpose of the National Heart, Lung, and Blood In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca2cfc5c1d61f7949c7d82ff56dcd7d8
https://pubmed.ncbi.nlm.nih.gov/24381984
https://pubmed.ncbi.nlm.nih.gov/24381984
Publikováno v:
Clinical Experimental Allergy. 25:29-32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d7a7ef58b02f9fd798fc1479e4b132f
https://doi.org/10.1111/j.1365-2222.1995.tb00416.x
https://doi.org/10.1111/j.1365-2222.1995.tb00416.x
Autor:
Richard C. Boucher, Christopher L. Karp, Frank J. Accurso, Pradeep K. Singh, William B. Guggino, Michael J. Welsh, John J. LiPuma, John F. Engelhardt, Susan Banks-Schlegel, Eric J. Sorscher, Paul B. McCray, Michael R. Knowles, Jay K. Kolls, Bonnie W. Ramsey, Ronald C. Rubenstein, Garry R. Cutting, Susan V. Lynch
Since the 1989 discovery that mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene cause cystic fibrosis (CF), there has been substantial progress toward understanding the molecular basis for CF lung disease, leading to th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b312b2c809041f0e5121ed498c42787
Autor:
Atul J. Butte, Carole Ober, A. Jake Lusis, David A. Schwartz, Weiniu Gan, Jack A. Elias, Susan Banks-Schlegel
Genome-wide association studies (GWAS) have revealed novel genes and pathways involved in lung disease, many of which are potential targets for therapy. However, despite numerous successes, a large proportion of the genetic variance in disease risk r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8d29c59e60ac1cd61b8d559199f3026
https://europepmc.org/articles/PMC2949401/
https://europepmc.org/articles/PMC2949401/
Publikováno v:
American journal of respiratory and critical care medicine. 170(7)
Cystic fibrosis (CF) is a genetic disease caused by autosomal recessive mutations of the CF transmembrane regulator, CFTR. CFTR functions in the plasma membrane of epithelial cells lining the lung, pancreas, liver, intestines, sweat duct, and the epi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd627079b0889b0d8485575285b7293a
https://pubmed.ncbi.nlm.nih.gov/15447951
https://pubmed.ncbi.nlm.nih.gov/15447951