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Sepsis from P. aeruginosa pneumonia induces a p53-independent decrease in gut epithelial proliferation. Despite an increase in sepsis-induced intestinal apoptosis, there is no compensatory increase in intestinal epithelial proliferation, and there is evidence of a cell cycle block with an accumulation of cells in M-phase. Decreasing gut apoptosis by overexpression of Bcl-2 is associated with a partial reversal of the effect of sepsis on the cell cycle.
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Coopersmith et al. (Sun,) studied this question.
www.synapsesocial.com/papers/69d8396e8c03fbaff8bee33f — DOI: https://doi.org/10.1097/01.ccm.0000055385.29232.11
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:
Craig M. Coopersmith
Paul E. Stromberg
Christopher G. Davis
Critical Care Medicine
Washington University in St. Louis
Progenitor Cell Therapy (United States)
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