IndraLab

Statements


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sparser
"In particular, C40-USP8 was used as a catalytically active mutant whereas the recently identified G664R USP8 mutant located in the autoinhibitory region was included in this study for further investigation [ xref , xref ]."

sparser
"However, cell transfection with S718del USP8 and C40-USP8 mutants in in vitro sensitive cultures from USP8 wild-type tumors abolished their ability to respond to pasireotide and did not confer pasireotide responsiveness to the in vitro resistant culture."

sparser
"Two of the four in vitro sensitive tumors (−17.1 ± 5.7% and −29.3 ± 1.1% secretion vs. basal for tumors #1 and #2, respectively, p < 0.05) were transiently transfected with S718del USP8 mutant while the remaining two in vitro sensitive tumors (−38.2 ± 2% and −22.7 ± 3.5% secretion vs. basal for tumors #4 and #5, respectively, p < 0.05) with the C40-USP8 mutant."

sparser
"Cell transfection with S718del USP8 and C40-USP8 mutants in responsive primary cultures bearing wild-type USP8 caused a complete loss of their ability to respond to the antisecretory action of pasireotide."