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Figure 2 TEM images of ZnS Mn and ZnS Mn/ZnO nanoparticles.a ZnS Mn.b ZnS Mn/ZnO(1).c HRTEM iamge of a single ZnS Mn nanoparticle.d HRTEM image of ZnS Mn/ZnO(1) nanoparticle showing the interface between shell and core.
Likewise, the functional differentiation between shell and core has received extensive coverage in the literature (for reviews, see Cardinal et al. 2002; Di Chiara 2002; Kelley 2004).
As discussed previously (Van Dongen et al. 2005), MSN recurrent axon collaterals might also be the substrate for communication between shell and core of the Acb.
The distinction between shell and core on the basis of (immuno)histochemical and connectional criteria has been described extensively since its recognition by Zaborszky and colleagues (1985; for reviews, see Groenewegen et al. 1996, 1999; Zahm 1999).
The parameter we compared quantitatively between shell and core neurons, i.e., the degree of overlap between the dendritic and axonal arborizations, did not show significant differences between neurons in these two subregions of the Acb.
Passive membrane properties and spontaneous synaptic transmission of MSNs from master mice were different in the NAc shell versus core before cocaine re-exposure, consistent with previous observations using non-contingent administration (Martin et al., 2006), in which opposite changes in excitability of MSNs were reported between shell and core.
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However, due to the surface area differences between the shell and core electrodes, the matching of the capacitance on both electrodes become a challenging task.
As can be seen in Fig. 13, three axonal branches traversed the border between the shell and core (cf also Van Dongen et al. 2005).
LL-induced split rhythms at the behavioral level correspond to anti-phase rhythms between the left and right SCN [ 13– 16], as well as anti-phase rhythms between the shell and core within each SCN lobe [ 13, 16].
To differentiate between the Acb shell and core subregions, as well as between the compartments therein, we employed the immunoreactivity patterns of the calcium-binding protein calbindin-D28 kDa (CaB) as an established maker (Fig. 2).
Furthermore, there can be strong differences between the spectrograms of the shell and core for the same drug and concentration, as for cytochalasin at 10 μg/ml.
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