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However, the autophagic response can also function as a protective mechanism allowing the recycling of proteins and cellular components to survive cell injuries induced by cytotoxic agents.
The cells were then treated 48 h with IgE-IC or anti-CD23 McAb before being incubated with parasites and the results clearly indicate that parasites fail to survive cell activation (Figure 1, lower panel).
The observation that 90% of CD44+/CD24-/ESA+ CD44+/CD24-/ESA+U label in an untreated asyncellsously diving culturetaingests that one mechanism BrdUhich these celabelreferentinlly survive cell cycle inhibitory anents countreatedasynchronously more slowly or remain quiescent comparediving the bulk of the line.
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In order to survive, cells must react through an osmoadaptative response.
The surviving cell fraction was used for further analysis.
Ribozymes were rescued from these surviving cell population and characterized by cloning and sequence analysis.
Surviving cell counts were normalized to unirradiated cultures.
First, the surviving cell population could be selected to survive because those cells have more mushroom spines or functional synapses.
Of the surviving cell masses and embryonic structures, most but not all were GFP+.
Unfortunately, the surviving cell clones are resistant to standard cytotoxic chemotherapies as well.
After two or three weeks, surviving cell colonies were picked up using cloning rings.
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