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1 e interregional variation in cortical neural architectonics.
2     Based on quantitative cyto- and receptor architectonic analyses, we identified 35 prefrontal area
3 iled dunnart (Sminthopsis crassicaudata), an architectonic analysis alone was carried out, and compar
4 heres and processed them for cyto- and myelo-architectonic analysis.
5  using intracortical microstimulation and an architectonic analysis.
6 ained with myelin and cytochrome oxidase for architectonic analysis.
7 lobe has long been viewed as a collection of architectonic and functional subdivisions.
8 cal areas that have been distinguished using architectonic and retinotopic criteria.
9                                 Based on its architectonics and functionality, it resembled areas 12/
10                                 Although the architectonic appearance of the core areas did vary in c
11 lts demonstrate that PE, defined as a single architectonic area that contains a topographic map of th
12             We observed the same 15 distinct architectonic areas in 10 brains.
13 ers the use of OCT in fundamental studies of architectonic areas in the human brain and the pathologi
14 nterograde tracers injected into each of the architectonic areas that constitute this region.
15 w focuses on cytoarchitectonics and receptor architectonics as biological correlates of function and
16 ctions were defined in DL(C) by reference to architectonic borders and patterns of connections with o
17 mismatch in border location, indicating that architectonic borders are not aligned with the retinotop
18 quadrant) projects to a narrow "ventral V3." Architectonic borders for these dorsal and ventral strip
19 ochrome oxidase from the same cases provided architectonic borders of V2 that matched those indicated
20                                              Architectonic borders were established in Nissl and SMI-
21                 Aligning retinotopic maps to architectonic borders, we found a mismatch in border loc
22                                          The architectonic boundaries of mPFC areas were identified i
23 esulting from the injections were related to architectonic boundaries.
24 es of area 3a were determined and related to architectonic boundaries.
25 face of flattened cortex and were related to architectonic boundaries.
26 uirrels, possibly accounting for the sensory architectonic characteristics of this region.
27   Across brains, these areas have consistent architectonic characteristics, and in flat map reconstru
28 entiated neocortex with clear functional and architectonic cortical field boundaries, as well as disc
29                                              Architectonic criteria for the core, lateral belt, and p
30 e present study was to determine whether the architectonic criteria used to identify the core region
31 e present study was to determine whether the architectonic criteria used to identify the core, latera
32  but can be distinguished from lPPC based on architectonic criteria.
33 in areas 17 and 18 was assessed by examining architectonic data and by inspecting the labeling patter
34 grammatic access to the maps and to receptor architectonic data that are anchored to brain areas.
35                                         This architectonic dichotomy is consistent with differences i
36 between brain areas in terms of the relative architectonic differentiation of connected areas.
37 ell-intrinsic properties, coupling them with architectonic differentiation, the resulting laminar pro
38 en somewhat elusive due to the lack of clear architectonic divisions.
39 tricular radial glia (vRG) scaffold as a key architectonic feature of the developing neocortex.
40                                          The architectonic features of the ventroposterior nucleus (V
41        Consistent with this evidence, Ta has architectonic features that are internally somewhat vari
42 oining temporal intermediate region (Ti) has architectonic features that suggest higher order and pos
43 the present study, somatotopic organization, architectonic features, and patterns of connections were
44                              Based on shared architectonic features, the auditory cortex in human and
45 subunit mRNAs differed within and across the architectonic fields of sensory-motor cortex.
46 gation agreeing with recently shown receptor-architectonic GABAB receptor distribution in ACC, wherea
47                   Thus, in parallel with the architectonic gradient of laminar differentiation, there
48                                        These architectonic gradients are reflected in the connections
49 ependently of the connectional results using architectonic, histochemical, and immunocytochemical cri
50 rom the Center on Functional Engineered Nano Architectonics in Los Angeles and discusses key benchmar
51                  The MFS is a functional and architectonic landmark in the human brain.
52                                Area-specific architectonic landmarks and lamination were preserved in
53 rebrum, which align closely with established architectonic maps.
54 f postmortem tissue to construct structural, architectonic maps.
55                    As in other primates, the architectonic methods allowed us to distinguish the late
56 nstrate the design, syntheses, and molecular architectonics of cyclic dipeptide tethered naphthalimid
57            There also appears to be a common architectonic organization for some respiratory drive tr
58            This study focuses largely on the architectonic organization of areas within and near the
59 ntraparietal area), support the fine-grained architectonic partitioning of cortical areas described i
60 ed a striking correspondence of fine-grained architectonic partitioning schemes in humans and nonhuma
61 rofilament protein (NF) immunoreactivity and architectonic patterns were compared with connections on
62                    From area 23c and TSA the architectonic progression can be traced in three directi
63 eus and nucleus of the trapezoid body, shows architectonic refinement.
64  The results indicate that each of the three architectonic regions of the pulvinar has a distinctive
65                                        These architectonic results demonstrate that the pulvinar comp
66  connections of the primate cerebral cortex: architectonic similarity (structural model), spatial pro
67 that MRI similarity can be representative of architectonic similarity between cortical areas and (ii)
68                                              Architectonic similarity showed the strongest and most c
69                                    Moreover, architectonic similarity was strongly related to the lam
70       Additionally, we found evidence for an architectonic subdivision within the parabelt, present i
71 ortex organization in other rodents in which architectonic subdivisions are not as obvious.
72                      Results were related to architectonic subdivisions of auditory cortex in brain s
73 emical staining with the SMI-32 antibody, 17 architectonic subdivisions were identified that are larg
74                                          The architectonic type principle conceptualizes structural c
75 hich are sufficient for the emergence of the architectonic type principle on the level of inter-areal
76 chitectonically distinct areas plus numerous architectonic zones in individuals over a region coverin