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1  face identity (the converse should hold for ventral regions).
2 RNA, however, is also present outside of the ventral region.
3 hs of ventral leg structures in the anterior-ventral region.
4  region and high frequencies in the anterior ventral region.
5 eceptor density, with greater density in the ventral region.
6 nd survival, and increased maturation in the ventral region.
7 the computing of identity information in the ventral region.
8 region and greater S-opsin expression in the ventral region.
9 lamina: a caudal-dorsal region and a rostral-ventral region.
10 from the ventral fin base and innervates the ventral region.
11 l lung regions without markedly compromising ventral regions.
12  neither recrossing nor projecting back into ventral regions.
13  the task with colour stimuli activated more ventral regions.
14 ssociated target short gastrulation (sog) in ventral regions.
15 s of content-related ("what") predictions in ventral regions.
16 l cells, but oriented parallel to the lip in ventral regions.
17 regions, whereas type II neurons localize to ventral regions.
18 her their axons terminate in intermediate or ventral regions.
19 egions was not offset by loss of aeration in ventral regions.
20 stinct melanins in melanocytes in dorsal and ventral regions.
21  D2 receptor upregulation in dorsal, but not ventral, region.
22             The mean number of nerves in the ventral region (11.0 +/- 3.5 per section) was greater co
23 position by prevention of axonal growth into ventral regions, (2) the prevention of axonal extension
24 .001 from baseline) and derecruitment in the ventral regions (-6.9% +/- 5.2%; p < 0.001).
25 ecreased proliferation of progenitors in the ventral region and decreased expression of the ventral m
26 uctures with spatially segregated dorsal and ventral regions and layered apicobasal cellular organiza
27 0 and E12 is essential for the patterning of ventral regions and the generation of cell types that ar
28 ughout the CNS, including Wnt7a and Wnt7b in ventral regions and Wnt1, Wnt3, Wnt3a, and Wnt4 in dorsa
29  expression valence can also be decoded from ventral regions, and identity from lateral regions.
30 entricular (dorsal) and the suprachiasmatic (ventral) regions, and limits dorsally with the preoptic
31 ecapitulates spatially segregated dorsal and ventral regions, as well as the layered segregation of e
32 lder adults showed less activity in anterior-ventral regions associated with controlled use of semant
33                                              Ventral regions, associated with stimulus valuation, tra
34 ntle layer of the spinal cord limiting it to ventral regions at E11.5.
35                                       In the ventral regions both face-gender discrimination and biol
36 lion cells were observed within the temporal-ventral region by approximately 48 hpf, more than 8 hour
37                                         This ventral region can determine lateral embryonic cell fate
38 the pericardial cavity while the intervening ventral region closes to form the myocardial tube.
39                            Then the muscle's ventral region develops a slit that demarcates an anteri
40 lei of the torus semicircularis, whereas the ventral region did not show significant effects of stimu
41 es that the fossil snake was pale-colored in ventral regions; dorsal and lateral regions were green w
42 ng of lymphatics channels in both dorsal and ventral regions, findings which reflect the reduced lymp
43 d cells increased quickly in both dorsal and ventral regions from P2 and reached a peak at P8.
44 inal cord included penetration of axons into ventral regions from which they would normally be repell
45                     As a somite matures, the ventral region gives rise to a mesenchymal cell populati
46 l regions of the brain are contracted, while ventral regions have expanded, with F(2) hybrid data pro
47 ession of the neuroectodermal genes into the ventral region in snail mutant is a possible cause of de
48                                  Recently, a ventral region in the macaque temporal cortex, the poste
49 rsal regions and along cranial nerves in the ventral regions in the human brain.
50 micircular canal nerves project primarily to ventral regions including the TON, ventral DON, intermed
51 (i.e., color was cued), and alpha power from ventral regions increased when color was irrelevant.
52 d by Grem2, separate an initially homogenous ventral region into distinct ventral and intermediate sk
53        We hypothesize that the role of these ventral regions is to provide enhanced multiview/posture
54 d evidence for vaguely defined "dorsal" and "ventral" regions is emerging.
55       The small retina showed a hypocellular ventral region, loss of Fgf15, normally expressed in pro
56 lls were confined primarily to the monocular ventral region of dLGN.
57 ypes both in Drosophila and vertebrates; the ventral region of Drosophila is homologous to the dorsal
58    Dense terminal projections arose from the ventral region of M1, and moderate projections from LPMC
59    Significant apoptosis was detected in the ventral region of mutant embryos within the definitive e
60 ail gene locus, which are both active in the ventral region of pre-gastrulation embryos.
61 portion of Rt sent a heavy projection to the ventral region of the anterior Ec, whereas the more caud
62  the DRN and c-Fos expression in the lateral ventral region of the BNST.
63 y bulb, and netrin1b is expressed within the ventral region of the bulb.
64  the inferior colliculus, CR-IR began in the ventral region of the central core.
65 psilateral axonal tract that projects to the ventral region of the cervical spinal cord.
66                                          The ventral region of the chick embryo optic cup undergoes a
67 c receives additional input from an anterior-ventral region of the claustrum, which has been reported
68 nfined to the telencephalon and the anterior-ventral region of the diencephalon.
69 ) neuronal differentiation in the dorsal and ventral region of the dysraphic neural tube occurs remar
70        In the absence of Wnt1, the posterior-ventral region of the embryo is severely altered during
71 MP-4 receptor inhibits SCL expression in the ventral region of the embryo.
72                                    While the ventral region of the field forms the myocardial tube, t
73 activity of the Pipe sulfotransferase in the ventral region of the follicular epithelium that surroun
74 d pipe are required only within a restricted ventral region of the follicular epithelium.
75                                          The ventral region of the forebrain is also absent in oep mu
76 in of the homozygous mice, especially in the ventral region of the forebrain.
77 chanical stimulation of either the dorsal or ventral region of the forepaw in the injured limb, with
78 cting SOX17+ biliary progenitor cells to the ventral region of the gut requires the notch effector He
79 kx2.5 expression domain to the most anterior ventral region of the heart field.
80          This effect was most evident in the ventral region of the hippocampal formation.
81 creased proliferation of NSCs located in the ventral region of the hippocampus while the mitotic inde
82  task showed more activation in the anterior ventral region of the inferior/middle frontal gyrus (BA
83 e cochlea, a coiled structure located in the ventral region of the inner ear, acts as the primary str
84 larly expressed in the developing dorsal and ventral region of the medulla oblongata.
85 d to the interpeduncular nucleus (IP) in the ventral region of the midbrain-hindbrain transition.
86 gion near the Eustachian tube orifice at the ventral region of the middle ear cavity, consisting most
87  in the 8th nerve tract, and probably a very ventral region of the NA.
88 t, Six1 expression was first detected in the ventral region of the otic pit and later is restricted t
89             Their genes are expressed in the ventral region of the pharynx at early stages of embryog
90 ined with a higher frequency (77-82 Hz) in a ventral region of the premotor cortex to produce a third
91 ty was detected at embryonic day 12.5 in the ventral region of the rhombencephalon and spinal cord an
92 ontextual monitoring demands, whereas a more ventral region of the right prefrontal cortex showed ret
93               This defect is specific to the ventral region of the RPE.
94 b paralysis and extensive vacuolation of the ventral region of the spinal cord.
95 , except for slightly thinner sheaths in the ventral region of the spinal cord.
96 effects on oligodendrocyte production in the ventral region of the spinal cord; however, less is know
97 n CeA-PKCdelta neurons and terminates in the ventral region of the zona incerta (ZI), a subthalamic s
98 icated that both groups activated dorsal and ventral regions of an anterior-limbic network, but the B
99 f endogenous CamKII activity from dorsal and ventral regions of embryos revealed elevated activity on
100 econd class of cells, most commonly found in ventral regions of LAd, had longer latency responses, bu
101 eased the density of serotonergic axons with ventral regions of spinal segments L1-L5, (3) and that N
102 icant activation of DA release in dorsal and ventral regions of the basal ganglia of healthy voluntee
103 f cellular growth and differentiation within ventral regions of the developing CNS.
104  area Te1 labeled axons and terminals in the ventral regions of the dorsal and ventral subnuclei of t
105 tion of the Toll-Dorsal signaling pathway in ventral regions of the early embryo.
106 ch resource for analyzing how the dorsal and ventral regions of the embryo communicate with each othe
107 lanar contact with tissues of the lateral or ventral regions of the embryo could also contribute to t
108 l components within a BMP pathway to pattern ventral regions of the embryo.
109 t of the bulb associated with peripheral and ventral regions of the epithelium, our results challenge
110 mechanisms and general strategies at play in ventral regions of the forming spinal cord, where sonic
111 est that oep is also required in lateral and ventral regions of the gastrula margin.
112 ously demonstrated that hyperactivity within ventral regions of the hippocampus (vHipp) drives the do
113                               The dorsal and ventral regions of the hippocampus perform different fun
114 e theta is known to propagate from dorsal to ventral regions of the hippocampus, these data suggest t
115 o the visuomotor functions of the dorsal and ventral regions of the lateral pre-motor cortex.
116 rasting theories propose that the dorsal and ventral regions of the lateral prefrontal cortex are inn
117 ead space measured by EIT was reduced in the ventral regions of the lungs, and the dead-space/shunt r
118 nalis (BNST), posterior dorsal and posterior ventral regions of the medial amygdala (MePD and MePV, r
119 -transgression interactions were observed in ventral regions of the medial prefrontal cortex.
120                                              Ventral regions of the medulla oblongata of the brainste
121 cial and vagal lobes and periventricular and ventral regions of the medulla oblongata.
122 oendoscopes were too short to reach the most ventral regions of the mouse brain.
123  FOV and high spatial resolution in the most ventral regions of the mouse brain.
124 in severe pigmentation defects in dorsal and ventral regions of the mouse skin.
125 rvate the superficial and deep layers of the ventral regions of the mPFC.
126  coordinating development between dorsal and ventral regions of the neural tube.
127 t enhancers, which direct gene expression in ventral regions of the neurogenic ectoderm in response t
128 nhancers direct restricted expression within ventral regions of the neurogenic ectoderm.
129 by blocking its initiation in the dorsal and ventral regions of the presumptive eye.
130 projects into the CMZ, and are found only in ventral regions of the retina.
131 , or both peptides were also detected in the ventral regions of the rostral hypothalamus, dorsolatera
132 Prdxs and Trxs in groups of cells located in ventral regions of the spinal cord that express motor ne
133 erent inputs and project to intermediate and ventral regions of the spinal cord.
134 V2 functions as a BMP4 feedback inhibitor in ventral regions of the Xenopus embryo; (2) CV2 complexes
135                The misexpression of Giant in ventral regions of transgenic embryos results in the sel
136 of each ISV leave the aorta only between the ventral regions of two adjacent somites, and migrate dor
137 e elicited by static luminance cues, even in ventral regions of visual cortex that have traditionally
138  support the idea that dorsal, as opposed to ventral, regions of the striatum are a locus of vulnerab
139 erated lung tissue in the ventral and medial-ventral regions on quantitative lung CT-scan performed b
140 hibition accompanied by decrease in CBF from ventral region or sympathoexcitation accompanied by incr
141 mozygous mutant embryos developed with their ventral region outside of the yolk sac, had two independ
142 consists of a dorsal region (striatum) and a ventral region (pallidum).
143 ysis of the shape of the similarity space in ventral regions provides evidence for a continuum in the
144 l, and contextual information [3-5], whereas ventral regions regulate stress responses [6], anxiety-r
145 ory interactions, whereby genes expressed in ventral regions repress those expressed in more dorsal r
146 onitoring demands were emphasized, while the ventral region showed greater activation when external c
147          More posterior occipitotemporal and ventral regions showed higher accuracy in the static con
148  during the monitored search task and a more ventral region showing activation under the externally c
149                 For example, a predominantly ventral region shows strong functional connectivity to t
150 non-rearranging cells, and a more fluid-like ventral region surrounding the leading edge with smaller
151 iprocal striatonigral terminal fields, and a ventral region that receives a specific striatonigral pr
152 ollow from the anatomy and laterality of the ventral regions that interact with the dorsal attention
153 the contralateral lower visual field and the ventral region the contralateral upper visual field.
154  a concomitant impairment of gas exchange in ventral regions, thus leading to a significant increase
155 s on the apical constriction of cells in the ventral region to produce bending forces that drive tiss
156 entral, intermediate regions and part of the ventral region, Vd/Vc/Vi, and Vv) expressed high levels
157 ity between the posterior-dorsal and lateral-ventral regions was corroborated by a multivariate analy
158 dorsal mEC of rTg4510 slices, while those in ventral regions were comparatively preserved.
159                            MCs in dorsal and ventral regions were labeled selectively with Cre-depend
160 on, focusing Wnt1 signaling to the posterior-ventral region where it suppresses nodal expression.
161 nes and eventually populate either dorsal or ventral regions, where they present as transcriptionally
162 reliably activated middle-occipital temporal-ventral regions which are known to participate in the de
163 fect of task was much greater in dorsal than ventral regions, with object category and task relevance
164 hat stimulation of more rostral and somewhat ventral regions within an ICC lamina achieves lower thre

 
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