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The majority of the ILD functions shifted towards more contralateral locations compared with the no-noise condition.
As SNR decreased, the ILD50 of these Contra-selective ILD functions shifted even further towards more contralateral locations compared with the standard noise condition.
Figure 4C shows an exemplar monotonic ILD function for which the ILD50 shifted by 6 dB towards more contralateral locations, compared with the ILD50 of the ILD function in the no-noise condition, when background noise was introduced.
A similar mechanism and functional role could underlie our observation of a noise-induced shift of the monotonic ILD sensitivity functions in IC mostly to ILDs generated from more contralateral locations compared with the no-noise condition.
For the exemplar non-monotonic ILD function in Fig. 4D, the peak ILD in the presence of noise was shifted by 10 dB towards more contralateral locations, compared with the no-noise condition.
However, one prediction of the noise-induced shift of ILD functions to ILDs favouring more contralateral locations is that, in noise, there should be an apparent shift in perceived sound location to more lateral locations.
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Rats with 6 or more contralateral turns/min were classified as having a successful lesion.
In 6 of 11 patients, a precordial DF gradient was observed between the scar and the contralateral locations.
These were grouped into 18 after an initial analysis, combining contralateral locations where laterality was unimportant or where bruises were rare, for example, wrists (figure 1).
A recent study by Miller and Recanzone (2009), for instance, demonstrated highly accurate model estimates for contralateral locations using a local, unilateral population.
A corollary of the first property of contralateral organization is that any contralateral location should yield a larger response than any ipsilateral location.
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