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However, the molecular mechanism of how TAZ functions in renal cells remains elusive.
Direct application of snPt1 to in vitro cultures of renal cells induced significant cytotoxicity.
11671_2013_1651_MOESM1_ESM.ppt Additional file 1: Figure S1: Cytotoxicity of snPt1 in renal cells.
Other experimental data supports the notion of 'stemness' in particular renal cells.
Hepatic and renal cells were co-cultured in separate micro-chambers on a single chip.
The SDS-treated decellularized scaffolds were non-cytotoxic to primary human renal cells.
However, toxicological information of their effect on renal cells and the mechanisms involved remain sparse.
Swollen or fragmented mitochondria in renal cells were observed under the electronic microscope.
Nitric oxide (NO) is produced by inducible nitric oxide synthase (iNOS) in macrophages, hepatocytes, and renal cells.
The full nanoparticles are first taken up by renal cells of the cortex region before complete elimination.
Instead, other kinds of renal cells kept in culture were used to investigate cell-to-cell communication [55, 114].
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