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An A(2A )adenosine receptor agonist, ATL313, reduces inflammation and improves survival in murine sepsis models

BACKGROUND: The pathophysiology of sepsis is due in part to early systemic inflammation. Here we describe molecular and cellular responses, as well as survival, in A(2A )adenosine receptor (AR) agonist treated and untreated animals during experimental sepsis. METHODS: Sepsis was induced in mice by i...

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Bibliografiset tiedot
Päätekijät: Moore, Christopher C, Martin, Edward N, Lee, Grace H, Obrig, Tom, Linden, Joel, Scheld, W Michael
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2008
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2588444/
https://ncbi.nlm.nih.gov/pubmed/18937852
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2334-8-141
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