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By induction on derivations in MSO one easily proves that each theorem of MSO is mapped to some theorem of PFO.
In gerbils, Day and Semple (J Neurophy, 2011) also found frequency-dependent best ITDs in MSO neurons.
Alternatively, nonlinearities at the level of the IC could reflect convergence of inputs, for example, from binaural neurons in MSO, LSO, and DNLL (McAlpine et al., 1998).
A recent intracellular in vivo study in MSO neurons shows that inhibition does not produce internal delays (Franken et al., Nat Neurosci 2015), contrary to previous claims (Brand et al., Nature 2002).
It could perhaps be tested with binaural reverse correlation and/or retrograde tracing in MSO neurons, but of course this is quite challenging, especially if it has to be done in many cells.
We did not address the question of how cortical responses might be decoded, because the controversy we address arose from measurements of responses in MSO and IC, and because these are earlier in the auditory pathway.
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Schemas of hostility to women, sexual entitlement, and a need for control have been found in MSO-R whereas MSO-CM presented a greater sense of worthlessness.
Available studies (Mann and Hollin, 2001; Milner and Webster, 2005; Ward, 2000) on schemata in sexual offenders have found different key themes in MSO-CM and MSO-R that can be related to anger expression.
Planned post hoc analyses revealed a 60% decrease in CA1 proBDNF in MSO-infused hippocampus 6 hours after contextual fear conditioning that were further reduced in ASO-infused hippocampus (Fig. 7b).
The dendritic trees of the neurons in the MSO, as revealed in Silver-Nissl impregnated sections, were additionally labeled by fine dotted lines (and by open circles in Fig. 2) for the vectorization.
Thus, while the original stereausis model does not appear consistent with earlier data, our proposition is to strengthen the hypothesis, we show in the revised manuscript an analysis of in vivo intracellular recordings in gerbil MSO cells.
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