Sentence examples for In lsn from inspiring English sources

The results are generally in agreement with the ITER design assumptions, finding that λn and λT are correlated (λT∼1.2λn) and both λn and λT are on average 2.1 2.5 times larger in IWL configurations than in LSN.

The actual neuronal loss in PD is known to be greater in LSN compared to MSN, with the SFG relatively spared.

If there is little emergent support, then LSn should remain constant as genes are combined, while increases in LSn as concatenation sets get larger suggest emergent support.

This beneficial effect was also present in the LSN where an lack of a decrease in NeuN positive neurones was also observed (38.4 ± 8.7% surviving following early tolerisation versus 22.9 ± 5.6% in non-tolerised EAE mice analysed at the same timepoint of 105 days; Figure  5h-n, red bar and lines, p < 0.01).

A final observation regarding neuronal loss is that comparing early to late tolerisation a small (but still significant) difference was observed in ChAT positive motor neurones but not NeuN positive neurones in the LSN, whilst there are clear behavioural differences between early and late tolerised animals as shown in the EAE clinical scoring.

In the LSN, co-administration of SPD with the high dose of SCH23390 induced more FLI nuclei than either drug alone (p<0.01 vs SCH23390 alone; p<0.05 vs SPD alone; Figure 6 upper chart).

At 0.5 mg/kg (n=5), SCH23390 alone had no effect in the mPFC (p=0.054 vs vehicle), NAc shell (p=0.97 vs vehicle), NAc core (p=0.67 vs vehicle), and DLSt (p=0.87 vs vehicle), and increased FLI nuclei in the LSN (p<0.05 vs vehicle).

FLI nuclei in the mPFC and NAc were counted at anterior posterior 2.60 2.80 mm, relative to bregma, and those in the LSN, DLSt, and the core and shell of the NAc were counted at anterior posterior 2.10 2.30 mm, relative to bregma.

However, activation in the VL-PAG (at sites shown in Fig. 3) resulted in significant increases (P < 0.01) in the numbers of Fos-positive neurones evoked by fast rates of skin heating bilaterally in the LSN (Fig. 6A).

In contrast to regions where the infused side was more severely affected than the contralateral side, the severity of pathology in the LSN was similar on both sides (Fig.  3f, n).

A small subset of P301SBE mice showed mild tau pathology in the LSN at 2 weeks post-infusion, but only on the contralateral side, whereas more substantial pathology was observed on both sides at 1 month post-infusion (data not shown).