Carnesecchi, Stephanie <br/><br/>
NOX1 is responsible for cell death through STAT3 activation in hyperoxia and is associated with the pathogenesis of acute respiratory distress syndrome.  [electronic resource] 

 -  International journal of clinical and experimental pathology  2014 
 - 537-51 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1936-2625 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Case-Control Studies<br/>Caspase 3--metabolism<br/>Cell Death<br/>Cells, Cultured<br/>Disease Models, Animal<br/>Epithelial Cells--enzymology<br/>Female<br/>Humans<br/>Hyperoxia--enzymology<br/>Mice<br/>Mice, Inbred C57BL<br/>Mice, Knockout<br/>NADH, NADPH Oxidoreductases--deficiency<br/>NADPH Oxidase 1<br/>NADPH Oxidases--metabolism<br/>Phosphorylation<br/>Poly (ADP-Ribose) Polymerase-1<br/>Poly(ADP-ribose) Polymerases--metabolism<br/>Pulmonary Alveoli--enzymology<br/>RNA Interference<br/>Reactive Oxygen Species--metabolism<br/>Respiratory Distress Syndrome--enzymology<br/>STAT3 Transcription Factor--metabolism<br/>Signal Transduction<br/>Time Factors<br/>Transfection