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1 se of BMP signaling for the specification of ventroposterior cell fates.
2 m MGC and the inferior division (VPI) of the ventroposterior complex (VP).
3 N-ALK4 blocks gastrulation and dorsoanterior/ventroposterior defects that otherwise occur following l
4    We find that Gli2 is sufficient to induce ventroposterior development, functioning in the FGF-brac
5 ns from the second group affect formation of ventroposterior embryonic structures.
6 fit was found in a small volume covering the ventroposterior globus pallidus internus and adjacent su
7  which demonstrated that all PNs innervating ventroposterior glomeruli contact a protocerebral neurop
8 ic nuclei including: anterior pulvinar (Pa), ventroposterior inferior (VPI), ventroposterior superior
9 xidase enzyme activity than area 3b; (3) The ventroposterior inferior nucleus (VPI) of the thalamus p
10 neurons in the ventroposterior nucleus (VP), ventroposterior inferior nucleus (VPI), posterior group
11 n was upregulated within thalamic neurons in ventroposterior lateral (VPL) and ventroposterior medial
12 attern of thalamocortical afferents from the ventroposterior lateral (VPL) nucleus to SI; and 3) chan
13 nating in the ventrolateral (VL) nucleus and ventroposterior lateral (VPL) nucleus.
14 traditional ventroposterior medial (VPM) and ventroposterior lateral (VPL) subnuclei were easily iden
15 erior (VPI), ventroposterior superior (VPS), ventroposterior lateral (VPL), ventral lateral (VL), cen
16 were found in the ventroposterior medial and ventroposterior lateral (VPM/VPL) nuclei of the thalamus
17  into S2 labeled the ventroposterior medial, ventroposterior lateral and posterior thalamic nuclei; i
18 osterior medial, ventroposterior medial, and ventroposterior lateral nuclei.
19 cortical areas; and thalamic inputs from the ventroposterior lateral nucleus (VPL).
20 the cuneate nucleus of the brainstem and the ventroposterior lateral nucleus of the thalamus is compa
21 No evidence was found for a PAG input to the ventroposterior lateral parvicellular, ventroposterior m
22 size of the brainstem nuclei by 41%, and the ventroposterior lateral subnucleus (VPL) of the thalamus
23  ventral posterior and parvicellular part of ventroposterior lateral thalamic nuclei; and injections
24 ional connectivity was decreased between the ventroposterior lateral thalamus (VPL) and primary somat
25 principal source of ascending projections to ventroposterior lateral, posterior and intralaminar thal
26                              The traditional ventroposterior medial (VPM) and ventroposterior lateral
27  responses of thalamocortical neurons in the ventroposterior medial (VPm) nucleus to 200 and 400 msec
28 ngs were noted within the barrel cortex, the ventroposterior medial (VPM) nucleus, the posterior medi
29 sentation, consistent with the amount of the ventroposterior medial (VPM) thalamic nucleus devoted to
30 sker pad or of the corresponding area of the ventroposterior medial (VPM) thalamic nucleus.
31 mulus-evoked discharge of neurons within the ventroposterior medial (VPM) thalamus and barrel field (
32 ture in the TUNEL reaction were found in the ventroposterior medial and ventroposterior lateral (VPM/
33 neurons in ventroposterior lateral (VPL) and ventroposterior medial nuclei, where extracellular unit
34  test which factor is more important, TG and ventroposterior medial nucleus (VPM) neurons were longit
35 or touch was identified as separate from the ventroposterior medial parvicellular nucleus (VPMpc) for
36 o the ventroposterior lateral parvicellular, ventroposterior medial parvicellular, caudal PC, oval pa
37                                          The ventroposterior medial subnucleus (VPM) for touch was id
38 s was densely labeled, whereas the adjoining ventroposterior medial subnucleus, VPM, representing the
39 ally implanted electrodes to record from the ventroposterior medial thalamic nucleus (VPM) and primar
40 he primary somatosensory (SI) cortex and the ventroposterior medial thalamus (VPM) before and during
41 (noise) and enlarges the receptive fields of ventroposterior medial thalamus (VPM) cells, noradrenerg
42  the receptive fields of single cells in the ventroposterior medial thalamus (VPM) of urethane-anesth
43 n the primary somatosensory cortex (S1), the ventroposterior medial, and the posterior medial thalami
44 elays of the thalamus--the posterior medial, ventroposterior medial, and ventroposterior lateral nucl
45               Injections into S2 labeled the ventroposterior medial, ventroposterior lateral and post
46                                          The ventroposterior medialis parvocellularis (VPMpc) nucleus
47 vation of Nodal signaling in non-cardiogenic ventroposterior mesendoderm, either by misexpression of
48  similar to that of Gli2 and is expressed in ventroposterior mesoderm after Gli2.
49 associated with a defect in the formation of ventroposterior mesoderm.
50 tant in the formation of some derivatives of ventroposterior mesoderm.
51      The spatial restriction of blood in the ventroposterior-most region of cloche mutant embryos may
52 he mesencephalic-diencephalic border and the ventroposterior nucleus (VP) in the torus semicircularis
53            The architectonic features of the ventroposterior nucleus (VP) were visualized in coronal
54 o study the location of these neurons in the ventroposterior nucleus (VP), ventroposterior inferior n
55                     The dorsal region of the ventroposterior nucleus (VPd) projects to DP-PCN and rec
56 rojection from the ventral edge of the toral ventroposterior nucleus (VPv).
57 yer VI neurons from postnatal day 2 (P2), in ventroposterior nucleus neurons (VP) from P7, and in ret
58  the primary somatosensory cortex (area 3b), ventroposterior nucleus of the thalamus and cuneate nucl
59 oxide synthase) reveals that neuropil in the ventroposterior nucleus of the thalamus is enriched with
60  anterior pretectal nucleus, the tectum, the ventroposterior nucleus of the torus semicircularis, the
61 rom the hand and face representations in the ventroposterior nucleus to area 3b also remained unalter
62     Injections in areas 3b and 1 labeled the ventroposterior nucleus, whereas injections in S2 labele
63 hereas injections in S2 labeled the inferior ventroposterior nucleus.
64  dorsoanterior tissues at the expense of the ventroposterior ones.
65  are a critical determinant of dorsoanterior-ventroposterior pattern in vertebrate embryos.
66 ement was associated with stimulation of the ventroposterior portion of the internal globus pallidus.
67 the pronephric duct, which develops from the ventroposterior portion of the pronephric anlage, is mis
68  in addition to the five known ones, and the ventroposterior projection neurons (VP PNs) that relay t
69 esia in mice, through its projections to the ventroposterior region of the thalamus.
70                      (b) We newly identify a ventroposterior shh pallidal domain representing the bas
71 issues of the tail: the ventral fin, and the ventroposterior somites and vasculature.
72 lvinar (Pa), ventroposterior inferior (VPI), ventroposterior superior (VPS), ventroposterior lateral
73 icate that BMP signaling is activated in the ventroposterior tailbud to promote cell migration during
74 s (PB), lateral hypothalamus (LH), or medial ventroposterior thalamic nucleus (VPM) 7 days before inj
75    Punishment increased beta2 mRNA levels in ventroposterior thalamic nucleus and gamma2 mRNA levels
76  hypothalamic grey matter, the contralateral ventroposterior thalamus, the anterior cingulate cortex,
77 e the receptive field size of neurons in the ventroposterior thalamus.
78          No presynaptic NR1 was found in the ventroposterior thalamus.
79 iking enlargement of receptive fields in the ventroposterior thalamus.
80 educed dorsoanterior structures and expanded ventroposterior tissues, phenocopying the zebrafish chor
81 tations in the somatosensory area 3b and the ventroposterior (VP) nucleus of thalamus are affected by
82  and localized to the ventrolateral (VL) and ventroposterior (VP) thalamus, while that of a network c