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1 somedial, and paraventricular nuclei and the lateral area).
2 ions of this striatal area compared with the lateral area.
3 FC regions travel ventral to those from more lateral areas.
4 , dorsal area 46 (46d), ventral area 46, and lateral area 12.
5                                              Lateral area 29 (29l) has a dense granular layer II-IV a
6 aze include the anterior suprasylvian gyrus (lateral area 5, anterior inferior parietal cortex) and m
7 he anterior ectosylvian sulcus (AES); 10) or lateral area 6 were all without impact on the ability to
8 five prefrontal regions: medial area 9 (9m), lateral area 9 (9l), dorsal area 46 (46d), ventral area
9 ipid bilayers with constant normal pressure, lateral area, and temperature using the CHARMM potential
10 ral inferior area, TI, the temporal anterior lateral area, and the temporal posterior inferior area l
11 at segregate the LA into dorsal, medial, and lateral areas, and suggest that the LA should be further
12 y, cortical anatomy suggests that medial and lateral areas are directly connected and may thus operat
13 erged within the rostral ZI, with dorsal and lateral areas being most prominent.
14 ortical stimulation revealed that medial and lateral areas can exert significant functional impact on
15 rmal to the membrane and a set point for the lateral area derived from experimental Bragg spacings, c
16 ositioning of the developing foregut to more lateral areas, either on the right or left side of the e
17 most strongly labeled, whereas posterior and lateral areas exhibit only weak labeling.
18 ale vertical z-resolution coupled with large lateral area imaging, label-free, noncontact, and in sit
19 sregistration >6 mm occurring in anterior or lateral areas in 76%, in inferior areas in 16%, and at t
20                    Results demonstrated that lateral areas, including face-selective areas in the pos
21 al, and dorsomedial nuclei as well as in the lateral area of the hypothalamus.
22 herical quantum dot (QD) and three differing lateral areas of 4-monolayer-thick nanoplatelets (NPLs),
23 s and terminate ipsilaterally, mostly in the lateral areas of the caudal nucleus tractus solitarii.
24 g a variety of cell identities in dorsal and lateral areas of the early Drosophila embryo, including
25  the primary somatosensory area, whereas two lateral areas partially encircled auditory cortex and co
26 ayer curvature, bending elastic modulus, and lateral area per molecule.
27 eedforward hierarchy, with processing within lateral areas preceding the processing within ventral ar
28 cell membrane layers that reseal along their lateral area (resealing time of approximately <2 min).
29 st striking when comparing across medial and lateral areas, suggesting that these areas have distinct
30 tterns with unusually large micrometer-sized lateral areas (up to ~1 mum(2)) and periodicities (up to
31 e secondary visual cortex, especially in the lateral areas (V2L).
32 nuous MD was run in an ensemble in which the lateral area was restrained to fluctuate about a mean va
33              The highly activated medial and lateral areas were shared by homologous members, generat
34 amics in a small patch of 4Calpha-1 mm(2) in lateral area-which contains four orientation hypercolumn