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1 ynaptogenesis, elaboration and refinement of thalamocortical afferents.
2 ical changes guide subsequent alterations in thalamocortical afferents.
3 difying the source or pattern of activity in thalamocortical afferents.
4 pearance of the vibrissae-related pattern of thalamocortical afferents.
5 oximately 1 d after ingrowth of AChE-stained thalamocortical afferents.
6 i-I) was used in these same animals to label thalamocortical afferents.
7 rs IV and VI, indicating their regulation by thalamocortical afferents.
8 a pattern complementary to vibrissae-related thalamocortical afferents.
10 docarbocyanine perchlorate (DiI) labeling of thalamocortical afferents and Nissl and cytochrome oxida
11 ces using electrical stimulation of putative thalamocortical afferents, and flavoprotein autofluoresc
12 cortical activity, but not the patterning of thalamocortical afferents (application of TTX and transe
13 thalamic ventrobasal complex at P0 (just as thalamocortical afferents are innervating the cortex) an
14 that formed by the terminal distribution of thalamocortical afferents arising from the posterior nuc
16 ut not for the development and plasticity of thalamocortical afferent clustering into a barrel patter
17 receive dense but transient innervation from thalamocortical afferents during the first postnatal wee
18 2) alterations in the projection pattern of thalamocortical afferents from the ventroposterior later
19 ouse barrel cortex, evoked by stimulation of thalamocortical afferents in an in vitro slice preparati
21 ults are consistent with the conclusion that thalamocortical afferents in postnatal rats transiently
25 lopment is thought to control the process of thalamocortical afferent innervation, segregation, and p
26 estioned by findings that the segregation of thalamocortical afferents into a somatotopic barrel patt
27 terns that undergo substantial changes after thalamocortical afferents invade the cortical plate, sug
28 o determine whether the patterning of either thalamocortical afferents or intracortical projections d
29 ted dextran amine (BDA) into the MGV labeled thalamocortical afferent patches within layer III/IV and
30 nly 20% of the mouse pups had an established thalamocortical afferent pattern in the barrel cortex at
31 tion of TTX and transection of the ION after thalamocortical afferent patterns are established), have
33 in a decrease in the size of the patches of thalamocortical afferents representing the mystacial vib
34 reas the MZ integrates uni- and multisensory thalamocortical afferent streams, it may ultimately infl
35 genes are established before the arrival of thalamocortical afferents, suggesting that they are inde
36 -specific NR1 knockout (CxNR1KO) mice, while thalamocortical afferents (TCAs) develop rudimentary whi
37 erotonin (5-HT) levels influences developing thalamocortical afferents (TCAs) in primary somatosensor
38 remarkably precise, with organized arrays of thalamocortical afferents (TCAs) that project into disti
39 transporter (5HT-T) histochemistry to label thalamocortical afferents (TCAs), we found no obvious ab
41 ealed that layer I axons were collaterals of thalamocortical afferents that formed multiple divergent
42 retrograde messenger nor that they activate thalamocortical afferents, the two dominant hypotheses.
43 decrease in efficacy was more pronounced in thalamocortical afferents, thus introducing an imbalance
45 tical layer IV while alternately stimulating thalamocortical afferents (via medial geniculate or down
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