Cystic Fibrosis Transmembrane Conductance Regulator in Sarcoplasmic Reticulum of Airway Smooth Muscle. Implications for Airway Contractility

Rationale: An asthma-like airway phenotype has been described in people with cystic fibrosis (CF). Whether these findings are directly caused by loss of CF transmembrane conductance regulator (CFTR) function or secondary to chronic airway infection and/or inflammation has been difficult to determine...

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Dades bibliogràfiques
Publicat a:Am J Respir Crit Care Med
Autors principals: Cook, Daniel P., Rector, Michael V., Bouzek, Drake C., Michalski, Andrew S., Gansemer, Nicholas D., Reznikov, Leah R., Li, Xiaopeng, Stroik, Mallory R., Ostedgaard, Lynda S., Abou Alaiwa, Mahmoud H., Thompson, Michael A., Prakash, Y. S., Krishnan, Ramaswamy, Meyerholz, David K., Seow, Chun Y., Stoltz, David A.
Format: Artigo
Idioma:Inglês
Publicat: American Thoracic Society 2016
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Original Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4803085/
https://ncbi.nlm.nih.gov/pubmed/26488271
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.201508-1562OC
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