c It must be stressed that the results of this study are yet to be based on linguistic data, but future studies will investigate the lexicogrammatical manifestations of 'formal' and 'informal' BSL using systemic functional methods.
Our results provide evidence that association of Noc4p with pre-ribosomes can occur without the presence of Nop14p (Fig. 4), but future studies will have to show whether formation of the salt stable Noc4p-Nop14p SSU-processome subcomplex requires the presence of other SSU-processome components.
Therefore, phosphorylation regulates this aspect of coilin function, but future studies will be needed before a clear understanding of the mechanism behind these results is obtained.
At present we do not understand the significance of the disconnect between EDL mass and force in EMP animals but future studies will focus on understanding this observation.
Also, our study focused on a priori regions of interest, but future studies will also need to examine the role of the right hemisphere due to atypical functional lateralization of language reported in ASD (Kleinhans et al. 2008).
Use of a combination tablet theoretically should improve adherence to antisecretory therapy as compared with use of separate individual NSAID and antisecretory agents, but future studies will be necessary to prospectively study adherence and the effect on endoscopic or clinical outcomes.
This study design is cross-sectional because of data limitations, but future studies will be able to use several years of the Rule of Law Index in a transverse design, now that the survey methods are mature and data collection is ongoing.
Our findings suggest a trend towards greater growth suppression in tumours treated with bortezomib prior to doxorubicin treatment than those treated with doxorubicin alone, but future studies will benefit from using other drugs to which HCT-8 tumours show greater sensitivity or other tumours that are more sensitive to doxorubicin, in order to assess bortezomib's potential as a chemo-sensitizer.
Efforts such as those of the Allen Brain Institute have shed some light on these markers, but future studies will need to analyze specific neuronal subtypes in order to be sure that differences between aged neurons and young neurons are truly due to aging and not different neuronal subtypes.
