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Immunostaining analysis and whole-cell patch-clamp recordings showed that embryonic hippocampal and cortical neurons maintained basic cellular properties and functions, including normal, healthy neuronal phenotypes and electrophysiological characteristics, after being printed through thermal inkjet nozzles.
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In this study, we focused on the impact of the lack of epsin on basic cellular properties using MEFs and cell-free assays.
The pathway controls a cascade of signals that regulates many basic cellular properties, including proliferation, survival, motility, and angiogenesis.
Especially, signals regulating such basic cellular properties as survival, proliferation, differentiation and apoptosis have caught the fancy of molecular oncologists.
The basic cellular properties of human MeCP2 are maintained upon expression in Drosophila including chromatin association, interactions with human chromatin remodeling gene homologs, and post-translational modifications (Cukier et al., 2008; Vonhoff et al., 2012) which suggests, on a molecular basis, at least a subset of hMeCP2 functional capabilities are preserved.
DiI is a long-chain dialkylcarbocyanine lipophilic neuronal tracer, which does not affect cell viability, development or the basic cellular physiological properties.
Transcription factors are master regulators in orchestrating basic cellular behaviors and are responsible for critical cellular functions and cellular fate.
Cilia-dependent signaling affects very basic cellular functions and aspects including cellular polarity and cell cycle progression [1-3].
Conserved genes are involved in basic cellular activities and thus are required for all stages.
Tumorigenesis involves many fundamental alterations in basic cellular mechanisms and interactions with microenvironment.
Transcription is an essential component of basic cellular and developmental processes.
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