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Approximately 61,000 statements.
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Copyright (c) 2011-2012, Selventa. All rights reserved.
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we demonstrate that SR-BI prevents NO-induced cytotoxicity and that a highly conserved CXXS redox motif is required for the anti-NO cytotoxicity activity of SR-BI. Using genetically manipulated mice, we demonstrate that SR-BI-null mice have a 3- to 4-fold increase in tyrosine nitrated proteins in aorta and liver compared with wild-type littermates, indicating that expression of SR-BI prevents peroxynitrite formation in vivo.
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Selventa
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2014-07-03T14:30:42.507+02:00
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