Significados de cellular toxicity em inglês

The cellular toxicity of HNE-aSyn was significantly higher than other PTM species.

Scaffolds loaded with pre-differentiated hASCs do not affect cell proliferation and no cellular toxicity was observed.

Nevertheless, these approaches face significant challenges such as providing sufficient signal-to-noise, cellular toxicity, or unequivocal detection.

Although several mechanisms have been proposed to link protein misfolding to cellular toxicity, the connection remains enigmatic.

Mutant HTT is less palmitoylated and this reduction of palmitoylation accelerates its aggregation and increases cellular toxicity.

Importantly, DNG oligonucleotides exhibit robust unaided cellular uptake as compared to unmodified oligonucleotides without apparent cellular toxicity.

Herein we report a new class of NCp7 inhibitors that possess good antiviral activity with low cellular toxicity.

These structures may damage the brain and give rise to cerebral amyloid angiopathy, neuronal dysfunction, and cellular toxicity.

However, this compound is labile and readily oxidized, resulting in cellular toxicity and preventing its reliable application in this context.

In groups 5 and 6, cellular toxicity was presented.

The cellular toxicity of erufosine was determined in two OSCC cell lines and gene expression and enrichment analyses were performed.

Here, we used a large-scale RNAi screen to identify the human genes that critically determine the cellular toxicity of Cdk1 inhibition.

The prevention of cellular toxicity associated with local metabolism or transport, which cannot be addressed by routine monitoring, is worth investigating further.

In this study, we tried to identify proteins responding to the cellular toxicity in NSAIDs-treated primarily cultured cardiomyocytes using 2-D proteomic analysis.

These genes either are involved in mycolic acid biosynthesis or are overexpressed as a response to the buildup or cellular toxicity of INH.

In a preliminary structure-activity investigation, one umbrella compound, designated Spm8CHAS, was identified which inhibited both HIV and HSV infections with no cellular toxicity.