Loss of cystic fibrosis transmembrane conductance regulator impairs lung endothelial cell barrier function and increases susceptibility to microvascular damage from cigarette smoke.

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作者： Mary Beth,Brown ^[1] ; William R,Hunt ^[2] ; Julie E,Noe ^[2] ; Natalia I,Rush ^[2] ; Kelly S,Schweitzer ^[2] ; Thomas C,Leece ^[2] ; Aigul,Moldobaeva ^[3] ; Elizabeth M,Wagner ^[3] ; Steven M,Dudek ^[4] ; Christophe,Poirier ^[2] ; Robert G,Presson ^[5] ; Erich,Gulbins ^[5] ; Irina,Petrache ^[6]

作者单位： Department of Medicine, School of Medicine, Indiana University, Indianapolis, Indiana, USA ; Department of Physical Therapy, School of Health and Rehabilitation Sciences, Indiana University, Indianapolis, Indiana, USA. ^[1] Department of Medicine, School of Medicine, Indiana University, Indianapolis, Indiana, USA. ^[2] Department of Medicine, Johns Hopkins University, Baltimore, Maryland, USA. ^[3] Department of Medicine, University of Illinois, Chicago, Illinois, USA. ^[4] Department of Anesthesia, School of Medicine, Indiana University, Indianapolis, Indiana, USA. ^[5] Department of Medicine, School of Medicine, Indiana University, Indianapolis, Indiana, USA ; Richard L. Roudebush Veteran Affairs Medical Center, Indianapolis, Indiana, USA. ^[6]

关键词 COPD S1P ceramides cystic fibrosis sphingolipids

DOI 10.1086/675989

PMID 25006445

发布时间 2021-10-21

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Pulmonary circulation

2014年4卷2期

260-8页

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Loss of cystic fibrosis transmembrane conductance regulator impairs lung endothelial cell barrier function and increases susceptibility to microvascular damage from cigarette smoke.

Pulmonary circulation

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Pulmonary circulation

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Loss of cystic fibrosis transmembrane conductance regulator impairs lung endothelial cell barrier function and increases susceptibility to microvascular damage from cigarette smoke.

Pulmonary circulation

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Pulmonary circulation

相关期刊

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