Matches in Nanopublications for { ?s ?p "The upregulation of MAPK activity was detected in breast cancers [77], and ERK1/2, JNK and p38 were identified in the stimulation of uPA and uPAR expression [78, 79]. Furthermore, inhibition of ERK1/2 and p38 down-regulated the expression of uPA/uPAR, which resulted in the inhibition of migration and decreased cell proliferation of the highly invasive breast cancer cells MDA-MB-231 [" ?g. }
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- _5 value "The upregulation of MAPK activity was detected in breast cancers [77], and ERK1/2, JNK and p38 were identified in the stimulation of uPA and uPAR expression [78, 79]. Furthermore, inhibition of ERK1/2 and p38 down-regulated the expression of uPA/uPAR, which resulted in the inhibition of migration and decreased cell proliferation of the highly invasive breast cancer cells MDA-MB-231 [" provenance.
- _5 value "The upregulation of MAPK activity was detected in breast cancers [77], and ERK1/2, JNK and p38 were identified in the stimulation of uPA and uPAR expression [78, 79]. Furthermore, inhibition of ERK1/2 and p38 down-regulated the expression of uPA/uPAR, which resulted in the inhibition of migration and decreased cell proliferation of the highly invasive breast cancer cells MDA-MB-231 [" provenance.
- _5 value "The upregulation of MAPK activity was detected in breast cancers [77], and ERK1/2, JNK and p38 were identified in the stimulation of uPA and uPAR expression [78, 79]. Furthermore, inhibition of ERK1/2 and p38 down-regulated the expression of uPA/uPAR, which resulted in the inhibition of migration and decreased cell proliferation of the highly invasive breast cancer cells MDA-MB-231 [" provenance.
- _5 value "The upregulation of MAPK activity was detected in breast cancers [77], and ERK1/2, JNK and p38 were identified in the stimulation of uPA and uPAR expression [78, 79]. Furthermore, inhibition of ERK1/2 and p38 down-regulated the expression of uPA/uPAR, which resulted in the inhibition of migration and decreased cell proliferation of the highly invasive breast cancer cells MDA-MB-231 [" provenance.