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We have investigated, using fully reactive molecular dynamics (ReaxFF), the structural and dynamics aspects of the hydrogenation mechanisms of graphdiyne membranes.
Accordingly, we have investigated, using perforated patch-clamp techniques, if brief subthreshold signals could be involved in the induction of long-term corticostriatal synaptic plasticity.
Here, we have investigated, using patch-clamp recordings and optogenetic tools, the functional properties and synaptic integration of DA neurons, generated from neural stem/progenitor cells in mouse ventral mesencephalic neurospheres (VMNs), when grafted into striatum of organotypic mouse hemisphere slice cultures.
Here, we have investigated, using BRET, the molecular determinants involved in providing OX2 receptors with greater β-arrestin-ubiquitin complex stability.
These results are in accord with the data that we have investigated using fecal samples collected from 2003 to 2008 [ 10].
To date, we have investigated using stem cells to replace primary neurons and astrocytes in in vitro co-culture models [ 66].
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In this paper we have investigated this using a multistage model with five stages.
We have investigated this using Model 1 that describes a GCN4 mRNA with uORF1, uORF4 and the main GCN4 ORF.
We have investigated the use of in vivo fluorescence imaging using fluorocoxib A as a molecular probe for early detection and assessment of skin tumors in mouse models of NMSC.
Using the dystrophic sapje zebrafish, we have investigated the use of tyrosine kinase and other inhibitors to treat the dystrophic symptoms in this model of Duchenne muscular dystrophy.
We have investigated the use of a continuous, linear grading scheme for compositionally graded (metamorphic) InxGa1−xAs buffers on GaAs grown using MOCVD, which can be used as virtual substrates for optical emitters operating at wavelengths >1.2 μm.
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