Matches in Nanopublications for { ?s ?p "In cells stably transfected with empty vector, AVP rapidly stimulated ERK, JNK, and p38 activity (Fig. 7A), similar to what we have previously reported (11). However, in both clones stably expressing myr-Akt, AVP-induced activation of JNK was completely blocked, and activation of p38 MAP kinases was significantly reduced (Fig. 7A)." ?g. }
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- _5 value "In cells stably transfected with empty vector, AVP rapidly stimulated ERK, JNK, and p38 activity (Fig. 7A), similar to what we have previously reported (11). However, in both clones stably expressing myr-Akt, AVP-induced activation of JNK was completely blocked, and activation of p38 MAP kinases was significantly reduced (Fig. 7A)." provenance.
- _5 value "In cells stably transfected with empty vector, AVP rapidly stimulated ERK, JNK, and p38 activity (Fig. 7A), similar to what we have previously reported (11). However, in both clones stably expressing myr-Akt, AVP-induced activation of JNK was completely blocked, and activation of p38 MAP kinases was significantly reduced (Fig. 7A)." provenance.
- _5 value "In cells stably transfected with empty vector, AVP rapidly stimulated ERK, JNK, and p38 activity (Fig. 7A), similar to what we have previously reported (11). However, in both clones stably expressing myr-Akt, AVP-induced activation of JNK was completely blocked, and activation of p38 MAP kinases was significantly reduced (Fig. 7A)." provenance.