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1 iskers tended to show broad tuning along the rostrocaudal axis.
2 with well-defined thalamic input anchors the rostrocaudal axis.
3  neuronal cell types are organized along the rostrocaudal axis.
4 n HVC is organized preferentially within the rostrocaudal axis.
5 wo contexts, dependent on position along the rostrocaudal axis.
6 15) are differentially distributed along the rostrocaudal axis.
7 or the responsiveness of the cells along the rostrocaudal axis.
8 issociable responses were identified along a rostrocaudal axis.
9 rded in Nkx2.2-null mutants along the entire rostrocaudal axis.
10  regions of Purkinje cell activity along the rostrocaudal axis.
11  patterning of the ventral midline along the rostrocaudal axis.
12 onal information that is laid down along the rostrocaudal axis.
13 th targets located more inferiorly along the rostrocaudal axis.
14 ual motor hotspot locations varied along the rostrocaudal axis.
15 heir inactive surround were mapped along the rostrocaudal axis (1.4-4.2 mm anterior to bregma) in cor
16 ojection is topographically organized in the rostrocaudal axis, along which sound azimuth is represen
17 n a few cells approximately midway along the rostrocaudal axis and also in a conspicuous group of ant
18 ajority of the chains are oriented along the rostrocaudal axis and many join the rostral migratory st
19 choice point that abnormally extended in the rostrocaudal axis and ventrally to the horizontal myosep
20 for cortical area were distributed along the rostrocaudal axis, and there was a reduced length of the
21  determining the migration of CINs along the rostrocaudal axis are less well understood.
22 pic transplantation of rhombomeres along the rostrocaudal axis at various developmental stages, we ha
23             Most embryos cut parallel to the rostrocaudal axis between the trunk paraxial mesoderm an
24  varied within and between nuclei, along the rostrocaudal axis, between cell types, and across develo
25 mice displayed impaired topognosis along the rostrocaudal axis but with little effect on left-right d
26 vealing three broad functional zones along a rostrocaudal axis composed of 2-4 smaller subregions eac
27 ts suggest that neural crest cells along the rostrocaudal axis display a graded loss in developmental
28 ontinuing capacity for interaction along the rostrocaudal axis, exemplified by the generation of the
29  in controlling motor neuron fates along the rostrocaudal axis, exemplified by the precise pattern of
30 w a preferential migration pattern along the rostrocaudal axis for medial- or caudal-born CINs.
31 or neurons from distinct positions along the rostrocaudal axis generally innervate muscles or muscle
32 roups of premigratory neural crest along the rostrocaudal axis have different propensities to contrib
33 ox transcription factors expressed along the rostrocaudal axis; however, the developmental mechanisms
34 th the formation of Probst bundles along the rostrocaudal axis in both mutants.
35  amplifying hierarchical organization on the rostrocaudal axis in larger brains.
36 uential factors may vary spatially along the rostrocaudal axis in the head.
37 mporal activation of BMP signaling along the rostrocaudal axis, in the dorsal neural tube, in the not
38 ctivity from dorsal to ventral PAG along the rostrocaudal axis mirrors structural and functional neur
39 also perturbed regional patterning along the rostrocaudal axis of neocortex.
40 um are topographically organized such that a rostrocaudal axis of origin is related to a medial-to-la
41 erficial gray layer (SGL) across most of the rostrocaudal axis of SC.
42 oproximal axis in subiculum are related to a rostrocaudal axis of termination in the entorhinal corte
43 ic currents of isolated hair cells along the rostrocaudal axis of the AP.
44 ion of the RPTPrho and FGF-1 boundary on the rostrocaudal axis of the cerebellar cortex was close to,
45 ilar placement of these injections along the rostrocaudal axis of the cord and that no tracer had spr
46 rchitectonic cortical gradients, and not the rostrocaudal axis of the cortex, are closely linked to t
47  of otic placode-inducing activity along the rostrocaudal axis of the embryo, and have determined tha
48 ociceptive responses is consistent along the rostrocaudal axis of the female rat spinal cord.
49 tation formed a mirror image of S2 along the rostrocaudal axis of the forelimb and hindlimb regions a
50 tation formed a mirror image of S1 along the rostrocaudal axis of the head region corresponding to th
51 e sections cryocut at 10-13 levels along the rostrocaudal axis of the LC.
52 motoneurons in restricted patterns along the rostrocaudal axis of the lumbosacral (LS) spinal cord.
53 phrinA ligands (TKO), thought to specify the rostrocaudal axis of the map, the projection on the coll
54 bustly innervates discrete columns along the rostrocaudal axis of the midbrain periaqueductal gray (P
55  about the molecular events that specify the rostrocaudal axis of the neural plate.
56 roectodermal cells positioned throughout the rostrocaudal axis of the neural tube, rather than at res
57    Most head pitch cells discharged when the rostrocaudal axis of the rat's head was orthogonal to th
58 zation, which is much more evident along the rostrocaudal axis of the SC than in the medial-lateral d
59 e generated at different positions along the rostrocaudal axis of the spinal cord, and the signals th
60 f the pMN/p3 domain boundary along the whole rostrocaudal axis of the spinal cord.
61 e motor neuron positional identity along the rostrocaudal axis of the spinal cord.
62 e generated at different positions along the rostrocaudal axis of the spinal cord.
63 triatum and pallidum are stretched along the rostrocaudal axis of the telencephalon.
64 l extension are widely distributed along the rostrocaudal axis of the zebrafish brain, but the cues f
65 totopic organization along the longitudinal (rostrocaudal) axis of the brain stem that was consistent
66      They were dispersed primarily along the rostrocaudal axis or in multiple directions, e.g., along
67        V2b inhibition is patterned along the rostrocaudal axis, providing long-range inhibition to mo
68  stimulus sites and CCEP responses along the rostrocaudal axis, regression analysis revealed a consis
69 ized in a precise tonotopic manner along the rostrocaudal axis, spanning the entire rostrocaudal exte
70 tion revealed clear specialization along the rostrocaudal axis such that the control of successive st
71 ensitive neurons were more restricted in the rostrocaudal axis than either the PND13-21 or PND22-28 S
72 system, the neural tube, is shaped along the rostrocaudal axis through two consecutive, radically dif
73 st, via optogenetic mapping of output in the rostrocaudal axis, we demonstrate that V2b neurons robus
74 Cell staining changes dramatically along the rostrocaudal axis, with neuronal labeling confined to re
75 y fibers across 10 distinct lobules over the rostrocaudal axis, with tactile receptor afferents preva