Source:http://linkedlifedata.com/resource/pubmed/id/16273323
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2006-2-16
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pubmed:abstractText |
Oxidative stress is involved in progression of left ventricular hypertrophy and heart failure. Since NADPH oxidases are a major source of reactive oxygen species in the heart, we studied left ventricular remodeling after myocardial infarction in mice with targeted deletion of the NADPH oxidase subunit gp91(phox).
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0300-8428
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
101
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
127-32
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:16273323-Animals,
pubmed-meshheading:16273323-Echocardiography,
pubmed-meshheading:16273323-Gene Deletion,
pubmed-meshheading:16273323-Membrane Glycoproteins,
pubmed-meshheading:16273323-Mice,
pubmed-meshheading:16273323-Mice, Knockout,
pubmed-meshheading:16273323-Myocardial Infarction,
pubmed-meshheading:16273323-NADPH Oxidase,
pubmed-meshheading:16273323-Oxidative Stress,
pubmed-meshheading:16273323-Ventricular Remodeling
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pubmed:year |
2006
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pubmed:articleTitle |
Left ventricular remodeling after myocardial infarction in mice with targeted deletion of the NADPH oxidase subunit gp91PHOX.
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pubmed:affiliation |
Medizinische Universitätsklinik Würzburg, Josef-Schneider Str. 2, 97080 Würzburg, Germany. frantz_s@medizin.uni-wuerzburg.de
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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