ライフサイエンスコーパス: parahippocampal place area

1 ]) and for the spatial layout of scenes (the parahippocampal place area).

2 onse observed with functional imaging in the parahippocampal place area.

3 ated with a face was only represented in the parahippocampal place area.

4 scenes and might be the homolog of the human parahippocampal place area.

5 eavily overlap with the functionally defined parahippocampal place area.

6 strong functional connectivity with anterior parahippocampal place area.

7 with the anterior portion of scene-selective parahippocampal place area.

8 Finally, the parahippocampal place area-a scene-selective region impl

9 gnal from each subject's fusiform face area, parahippocampal place area and area MT/MST provided a me

10 and scene selectivity (including the "proto" parahippocampal place area and retrosplenial complex) by

11 ween category-level scene selectivity in the parahippocampal place area and subsequent memory perform

12 es are represented in the brain, in both the parahippocampal place area and the prefrontal cortex, re

13 lace, for example, a kitchen), including the parahippocampal place area, and "visually guided navigat

14 rea, lateral occipital cortex, mid fusiform, parahippocampal place area, and extending superiorly to

15 e to novel images in the fusiform face area, parahippocampal place area, and extrastriate body area,

16 fMRI revealed significant attenuation in the parahippocampal place area for only the repeated scenes

17 nd we demonstrate that a larger shift in the parahippocampal place area is associated with poorer mem

18 Moreover, one scene-selective region (the parahippocampal place area or PPA) was tolerant to mirro

19 found in other scene-selective regions (the parahippocampal place area or retrosplenial complex) or

20 ain include three scene-selective areas: the parahippocampal place area (or the temporal place areas)

21 FFA) (apparently selective for faces) to the parahippocampal place area (PPA) (apparently selective f

22 ion index in two regions of interest (ROIs): parahippocampal place area (PPA) and lateral occipital c

23 l cortex (LO) and scene-specific ROIs in the parahippocampal place area (PPA) and posterior collatera

24 nsion for scene-selective attenuation in the parahippocampal place area (PPA) and retrosplenial corte

25 distributed and complementary manner by the parahippocampal place area (PPA) and the lateral occipit

26 participants showed strong activation of the parahippocampal place area (PPA) and the retrosplenial c

27 e showed a stronger functional connection to parahippocampal place area (PPA) compared with adjacent

28 es of the human fusiform face area (FFA) and parahippocampal place area (PPA) during binocular rivalr

29 bserved from specific locations, whereas the parahippocampal place area (PPA) encodes sets of views c

30 The parahippocampal place area (PPA) has been demonstrated t

31 In humans, the ventral temporal parahippocampal place area (PPA) has been implicated in

32 al neuroimaging studies have argued that the parahippocampal place area (PPA) represents such navigat

33 For example, the parahippocampal place area (PPA) responds maximally to e

34 l vs. familiarity specific to words, and the parahippocampal place area (PPA) showed effects for reca

35 ions within the fusiform face area (FFA) and parahippocampal place area (PPA) was modulated such that

36 Here we show that the parahippocampal place area (PPA), a region in human occi

37 However, in the parahippocampal place area (PPA), a scene-selective regi

38 the fusiform face area (FFA), scenes in the parahippocampal place area (PPA), and bodies in the extr

39 ex, including the primary visual cortex, the parahippocampal place area (PPA), and the retrosplenial

40 hip between scene and object patterns in the parahippocampal place area (PPA), even though this regio

41 esponses in the fusiform face area (FFA) and parahippocampal place area (PPA), respectively.

42 ng elicited similar activity patterns in the parahippocampal place area (PPA), retrosplenial complex

43 hree gradients extending anteriorly from the parahippocampal place area (PPA), retrosplenial complex

44 We found that area V1, the parahippocampal place area (PPA), retrosplenial cortex (

45 scene-sensitive cortical region known as the parahippocampal place area (PPA), significant attenuatio

46 vely engaged in visual scene processing: the parahippocampal place area (PPA), the retrosplenial comp

47 has intact scene-selective responses in the parahippocampal place area (PPA), transverse occipital s

48 elective regions in human visual cortex [the parahippocampal place area (PPA), transverse occipital s

49 SC)/parietal-occipital sulcus region and the parahippocampal place area (PPA), which previous studies

50 level image features of the stimuli, and the parahippocampal place area (PPA), which showed better te

51 leus on generating selective response within parahippocampal place area (PPA).

52 vely respond to visual scenes, including the parahippocampal place area (PPA).

53 ate parametric effects in the MTL, mPFC, and Parahippocampal Place Area (PPA).

54 cluding the fusiform face area (FFA) and the parahippocampal place area (PPA).

55 llateral sulcus (CoS) that overlaps with the parahippocampal place area (PPA).

56 ved in high-level scene representations, the parahippocampal place area (PPA).

57 ast, landmark associations were coded in the parahippocampal place area (PPA).

58 area (FBA), retrosplenial complex (RSC) and parahippocampal place area (PPA).

59 control regions in bilateral scene-selective parahippocampal place areas (PPA).

60 This area (the parahippocampal place area [PPA]) was initially interpre

61 tive precuneus and in three scene-selective (parahippocampal place area [PPA], medial place area, occ

62 The "parahippocampal place area" (PPA) responds more strongly

63 This region, which we name the 'parahippocampal place area' (PPA), responds selectively

64 superior temporal sulcus, STS)- and place ('parahippocampal place area', PPA)-selective cortices in

65 "scene-selective" visual cortical area (the parahippocampal place area; PPA) showed distinctively hi

66 regions that respond selectively to scenes: parahippocampal place area, retrosplenial complex/medial

67 Interestingly, the visual parahippocampal place area showed NF activation closer t

68 (and one not for navigation at all): (i) The parahippocampal place area supports scene categorization

69 egions such as retrosplenial complex and the parahippocampal place area were sensitive to landmark re

70 erior cingulate cortex (PCC), as well as the parahippocampal place area, where tracking uniquely rela