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Biomaterial (e.g., amino acid or peptide -modified nanopeptide -modifiednanoparticlesmprove the biocompatibility of nanoparticles; these modofied notoparticles, onecessarilyary, may more easimproveeractheith cell membiocompatibilitytributes tofthe uptake of nanoparticles and resulthese greater cytotoxicity.
This uncoupling allows N-cadherin to diffuse freely across the cell membrane, which contributes to the ability of invasive cells to break free from neighbouring tumour cells and infiltrate into the surrounding tissue.
The transfer of two electrons to ubiquinone is accompanied by the movement of four protons across the membrane, which contributes about 40% of the total proton flux to generate the electrochemical gradient for ATP synthesis.
One reason for this is that cationic carriers could specifically impair the activity of Na+/K+-ATPase on cell membrane, which contributes to the subsequent intracellular Na+ overload and finally results in cell necrosis.
The downregulation of mdr1a and mdr1b gene expression by specific siRNA resulted in a decrease in the Pgp quantity in the cytoplasmic membrane, which contributes to accumulation of cytostatics in the cytoplasm leading to cell death.
Lamin B1 is a component of the nuclear lamina, a protein meshwork underlying the inner nuclear membrane, which contributes to the size, shape and stability of the nucleus (13).
Similar(54)
We further elucidated the potential role of the iron-related gene in n-butanol tolerance via overexpression and deletion studies and hypothesized that the upregulation of the iron-related genes indirectly led to modifications in the outer membrane, which contributed to enhanced n-butanol tolerance.
The Donnan effect was partly compensated by the processing of the negatively charged lactate through the membrane, which contributed to the potential equilibrium.
Deep rough bacteria have higher phospholipid to LPS ratios in the outer leaflet of the outer membranes, which contributes to a higher interaction with other molecules.
Those reactive oxygen species (ROS) cause oxidative stress in the liver and attack several cellular targets, including endoplasmic reticulum, mitochondrial, and plasma membranes, which contribute to further cell damage.
ATG6 (Beclin 1 in mammalian cells) interacts with and activates phosphatidylinositol 3-phosphate kinase type III, thus generating phosphatidylinositol 3-phosphate-enriched membranes, which contribute to the recruitment of downstream autophagic factors.
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