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Apoptosis could be inhibited using the pan-caspase inhibitor z-VAD-fmk (results not shown).
The avoidance behaviour to somatostatin in Sstr2 transgenic animals can be inhibited using the somatostatin antagonist cyclosomatostatin.
This process can be inhibited using the antimalarial agent chloroquine (CQ), which impairs lysosomal function and prevents autophagosome turnover.
Stimulation of these sweet taste receptors is important for glucose-stimulated secretion of GLP-1 in humans and can be inhibited using the sweet taste receptor antagonist lactisole (22).
It has been demonstrated previously that receptor activation can lead to the phosphorylation of PKB/Akt in SH-SY5Y cells, and that PKB phosphorylation can be inhibited using the PI3-kinase inhibitor, wortmannin [33].
Hyperosmolarity was also able to promote activation of gene expression through a COL2A1 enhancer element, a known target of SOX9, which could be inhibited using the p38 MAPK inhibitor SB202190.
Similar(54)
Functional confirmation of the relevance of these results for osteoblast morphological transitions came from experiments in which Shh hedgehog signalling was inhibited using the well-established pathway inhibitor cyclopamine (Cyc).
All excitatory synaptic activity recorded in BicPic was inhibited using the AMPA/kainite receptor antagonist NBQX (20 um).
SCD was inhibited using the small molecule inhibitor (4- 2-chlorophenoxy -N- 3- methylcarbamoyl -phenyl piperidine-1-carboxamide 4- 2-chlorophenoxy -N- 3- methylcarbamoyl -phenyl piperidine-1-carboxamide 4- 2-chlorophenoxy -N- 3- methylcarbamoyl -phenyl piperidine-1-carboxamide 4- 2-chlorophenoxy -N- 3- methylcarbamoyl -phenyl piperidine-1-carboxamide 4- 2-chlorophenoxy -N- 3- methylcarbamoyl -phenyl piperidine-1-carboxamide 4- 2-chlorophenoxy -N- 3- methylcarbamoyl -phenyl piperidine-1-carboxamide 4- 2-chlorophenoxy -N- 3- methylcarbamoyl -phenyl piperidine-1-carboxamide 4- 2-chlorophenoxy -N- 3- methylcarbamoyl -phenyl piperidine-1-carboxamide 4- 2-chlorophenoxy -N- 3- methylcarbamoyl -phenyl piperidine-1-carboxamide
pRb family members were inactivated in MCF-7 cells by expressing polyomavirus large tumor antigen (PyLT), and cdk activity was inhibited using the cdk inhibitors p16INK4A and p21Waf1/Cip1.
Trypsin was inhibited using the same volume of complete medium.
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CEO of Professional Science Editing for Scientists @ prosciediting.com