ライフサイエンスコーパス: architectonic

1 e interregional variation in cortical neural architectonics.

2 iled dunnart (Sminthopsis crassicaudata), an architectonic analysis alone was carried out, and compar

3 using intracortical microstimulation and an architectonic analysis.

4 ained with myelin and cytochrome oxidase for architectonic analysis.

5 heres and processed them for cyto- and myelo-architectonic analysis.

6 lobe has long been viewed as a collection of architectonic and functional subdivisions.

7 cal areas that have been distinguished using architectonic and retinotopic criteria.

8 Based on its architectonics and functionality, it resembled areas 12/

9 Although the architectonic appearance of the core areas did vary in c

10 lts demonstrate that PE, defined as a single architectonic area that contains a topographic map of th

11 We observed the same 15 distinct architectonic areas in 10 brains.

12 nterograde tracers injected into each of the architectonic areas that constitute this region.

13 ctions were defined in DL(C) by reference to architectonic borders and patterns of connections with o

14 mismatch in border location, indicating that architectonic borders are not aligned with the retinotop

15 quadrant) projects to a narrow "ventral V3." Architectonic borders for these dorsal and ventral strip

16 ochrome oxidase from the same cases provided architectonic borders of V2 that matched those indicated

17 Architectonic borders were established in Nissl and SMI-

18 Aligning retinotopic maps to architectonic borders, we found a mismatch in border loc

19 The architectonic boundaries of mPFC areas were identified i

20 esulting from the injections were related to architectonic boundaries.

21 es of area 3a were determined and related to architectonic boundaries.

22 face of flattened cortex and were related to architectonic boundaries.

23 uirrels, possibly accounting for the sensory architectonic characteristics of this region.

24 Across brains, these areas have consistent architectonic characteristics, and in flat map reconstru

25 entiated neocortex with clear functional and architectonic cortical field boundaries, as well as disc

26 Architectonic criteria for the core, lateral belt, and p

27 e present study was to determine whether the architectonic criteria used to identify the core region

28 e present study was to determine whether the architectonic criteria used to identify the core, latera

29 but can be distinguished from lPPC based on architectonic criteria.

30 in areas 17 and 18 was assessed by examining architectonic data and by inspecting the labeling patter

31 This architectonic dichotomy is consistent with differences i

32 en somewhat elusive due to the lack of clear architectonic divisions.

33 tricular radial glia (vRG) scaffold as a key architectonic feature of the developing neocortex.

34 The architectonic features of the ventroposterior nucleus (V

35 Consistent with this evidence, Ta has architectonic features that are internally somewhat vari

36 oining temporal intermediate region (Ti) has architectonic features that suggest higher order and pos

37 the present study, somatotopic organization, architectonic features, and patterns of connections were

38 Based on shared architectonic features, the auditory cortex in human and

39 subunit mRNAs differed within and across the architectonic fields of sensory-motor cortex.

40 gation agreeing with recently shown receptor-architectonic GABAB receptor distribution in ACC, wherea

41 Thus, in parallel with the architectonic gradient of laminar differentiation, there

42 These architectonic gradients are reflected in the connections

43 ependently of the connectional results using architectonic, histochemical, and immunocytochemical cri

44 rom the Center on Functional Engineered Nano Architectonics in Los Angeles and discusses key benchmar

45 Area-specific architectonic landmarks and lamination were preserved in

46 rebrum, which align closely with established architectonic maps.

47 f postmortem tissue to construct structural, architectonic maps.

48 As in other primates, the architectonic methods allowed us to distinguish the late

49 There also appears to be a common architectonic organization for some respiratory drive tr

50 This study focuses largely on the architectonic organization of areas within and near the

51 ntraparietal area), support the fine-grained architectonic partitioning of cortical areas described i

52 ed a striking correspondence of fine-grained architectonic partitioning schemes in humans and nonhuma

53 rofilament protein (NF) immunoreactivity and architectonic patterns were compared with connections on

54 From area 23c and TSA the architectonic progression can be traced in three directi

55 The results indicate that each of the three architectonic regions of the pulvinar has a distinctive

56 These architectonic results demonstrate that the pulvinar comp

57 connections of the primate cerebral cortex: architectonic similarity (structural model), spatial pro

58 Architectonic similarity showed the strongest and most c

59 Moreover, architectonic similarity was strongly related to the lam

60 Additionally, we found evidence for an architectonic subdivision within the parabelt, present i

61 ortex organization in other rodents in which architectonic subdivisions are not as obvious.

62 Results were related to architectonic subdivisions of auditory cortex in brain s

63 emical staining with the SMI-32 antibody, 17 architectonic subdivisions were identified that are larg

64 chitectonically distinct areas plus numerous architectonic zones in individuals over a region coverin