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000136759 0247_ $$2doi$$a10.1093/cercor/bhs009
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000136759 0247_ $$2ISSN$$a1047-3211
000136759 0247_ $$2ISSN$$a1460-2199
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000136759 037__ $$aDZNE-2020-03081
000136759 041__ $$aEnglish
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000136759 1001_ $$0P:(DE-2719)2191623$$aMüller, Notger G$$b0$$eFirst author
000136759 245__ $$aRepetition suppression versus enhancement--it's quantity that matters.
000136759 260__ $$aOxford$$bOxford Univ. Press$$c2013
000136759 264_1 $$2Crossref$$3online$$bOxford University Press (OUP)$$c2012-02-07
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000136759 520__ $$aUpon repetition, certain stimuli induce reduced neural responses (i.e., repetition suppression), whereas others evoke stronger signals (i.e., repetition enhancement). It has been hypothesized that stimulus properties (e.g., visibility) determine the direction of the repetition effect. Here, we show that the very same stimuli can induce both repetition suppression and enhancement, whereby the only determining factor is the number of repetitions. Repeating the same, initially novel low-visible pictures of scenes for up to 5 times enhanced the blood oxygen level-dependent (BOLD) response in scene-selective areas, that is, the parahippocampal place area (PPA) and the transverse occipital sulcus (TOS), presumably reflecting the strengthening of the internal representation. Additional repetitions (6-9) resulted in progressively attenuated neural responses indicating a more efficient representation of the now familiar stimulus. Behaviorally, repetition led to increasingly faster responses and higher visibility ratings. Novel scenes induced the largest BOLD response in the PPA and also higher activity in yet another scene-selective region, the retrospenial cortex (RSC). We propose that 2 separable processes modulate activity in the PPA: one process optimizes the internal stimulus representation and involves TOS and the other differentiates between familiar and novel scenes and involves RSC.
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000136759 650_2 $$2MeSH$$aAdolescent
000136759 650_2 $$2MeSH$$aAdult
000136759 650_2 $$2MeSH$$aBrain: physiology
000136759 650_2 $$2MeSH$$aBrain Mapping
000136759 650_2 $$2MeSH$$aFemale
000136759 650_2 $$2MeSH$$aHumans
000136759 650_2 $$2MeSH$$aMagnetic Resonance Imaging
000136759 650_2 $$2MeSH$$aMale
000136759 650_2 $$2MeSH$$aPhotic Stimulation
000136759 650_2 $$2MeSH$$aRecognition, Psychology: physiology
000136759 650_2 $$2MeSH$$aYoung Adult
000136759 7001_ $$0P:(DE-HGF)0$$aStrumpf, H.$$b1
000136759 7001_ $$0P:(DE-HGF)0$$aScholz, M.$$b2
000136759 7001_ $$0P:(DE-HGF)0$$aBaier, B.$$b3
000136759 7001_ $$0P:(DE-HGF)0$$aMelloni, L.$$b4
000136759 77318 $$2Crossref$$3journal-article$$a10.1093/cercor/bhs009$$b : Oxford University Press (OUP), 2012-02-07$$n2$$p315-322$$tCerebral Cortex$$v23$$x1047-3211$$y2012
000136759 773__ $$0PERI:(DE-600)1483485-6$$a10.1093/cercor/bhs009$$gVol. 23, no. 2, p. 315 - 322$$n2$$p315-322$$q23:2<315 - 322$$tCerebral cortex$$v23$$x1047-3211$$y2012
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000136759 9141_ $$y2013
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