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This region contained two potential γ-interferon-activated sites (GASs) that could be activated by different signal transducer and activator of transcription (STAT) proteins [ 21],[ 22].
Despite the high amino acid sequence homology between PIEZO1 and PIEZO2, these two channels appear to be activated by different kinds of mechanical stimuli.
To this end, it is important to note that the same causal mechanism might be activated by different security measures, reflecting variations in context.
These RhoGEFs are likely to be activated by different signals as unc-73 is regulated by Gαq [68] while rhgf-1 acts downstream of Gα12 [69].
This kinase can be activated by different extracellular signals and regulates protein synthesis at the initiation level mainly through the phosphorylation of at least two downstream targets, p70S6 kinase (p70S6K) and eukaryotic initiation factor 4E-binding proteins (4E-BPs, see for references, [8]).
Oncogenic pathways can be activated by different molecular mechanisms.
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In this work, we show that these enhancers have distinct spatio-temporal activities and are activated by different signaling pathways.
These xenosensors are known to exhibit different molecular biology and mechanisms of activation, in addition to being activated by different agonists [ 33– 33].
Src-family tyrosine kinases associate with and regulate the activity of L-type VDCCs [ 76], and are activated by different members of the immunoglobulin superfamily including NCAM [ 77] and L1 [ 78].
We hypothesize the effectiveness of the SDSS might be explained by different sets of muscle fibers being activated by different electrodes, and, therefore, the increased time between subsequent activation of motor units allows their greater recovery.
Platelet activation occurs through numerous signalling cascades that originate from diverse surface receptors being activated by different agonists.
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