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1 erior tuber nuclei), and telencephalon (area ventralis).
4 g, asymmetry in the motor nucleus and in the ventralis and dorsalis syrinx muscles was also tested.
5 ular nuclei (composed of the gigantocellular ventralis and pars alpha nuclei as well as the adjacent
6 ughout the embryo, the inner ear is severely ventralised and medialised, in addition to displaying th
7 henotype in which the anterior of the egg is ventralised and the posterior dorsalised, demonstrating
8 al for ventral cell fate and that subsets of ventralising and dorsalising genes require GATA activity
9 porter mRNA in the dorsal raphe dorsalis and ventralis, and increases in glucocorticoid receptor mRNA
10 ensory thalamic nucleus dorsalis intermedius ventralis anterior (DIVA) is consistent with the well-kn
11 l [ventralis lateralis pars oralis (VLo) and ventralis anterior (VA)] and cerebellar [ventralis later
12 Subsequently, Bmp7 acts on cells that are ventralised by Shh, establishing aspects of hypothalamic
13 dorsalising factors and lower levels of the ventralising factors act in concert to induce the myotom
15 hali (LM), and n. geniculatus lateralis pars ventralis (GLv), are prominent retinorecipient structure
19 umed to arise predominantly from the nucleus ventralis intermedius (Vim) of the thalamus, the implant
20 tandard atlas, and a 3D model of the nucleus ventralis intermedius and adjacent structures was create
21 d from the posterior subthalamic area to the ventralis intermedius nucleus and coincided with a norma
22 stimulation among 28 patients who underwent ventralis intermedius nucleus deep brain stimulation and
24 ded focused ultrasound surgery targeting the ventralis intermedius nucleus of the thalamus contralate
25 ed focused ultrasound surgery of the nucleus ventralis intermedius of the thalamus commonly evokes tr
26 ents receiving deep brain stimulation of the ventralis intermedius thalamic nucleus for essential tre
29 of dual-lead thalamic DBS (one targeting the ventralis intermedius-ventralis oralis posterior nucleus
30 our observations to neurons in the pallidal [ventralis lateralis pars oralis (VLo) and ventralis ante
31 e pallidal receiving area of motor thalamus (ventralis lateralis pars oralis, VLo) (38%, 21/55 cells)
32 and ventralis anterior (VA)] and cerebellar [ventralis lateralis posterior pars oralis (VPLo)] receiv
33 phalon, and neurons were labeled in the area ventralis of Tsai (AVT), the substantia nigra (nucleus t
34 the hippocampus, septum, hypothalamus, area ventralis of Tsai, and substantia nigra, where they form
35 ratum griseum et fibrosum superficiale, area ventralis of Tsai, n. tegmenti pedunculopontinus pars co
37 border [the VIM lead] and one targeting the ventralis oralis anterior-ventralis oralis posterior bor
38 one targeting the ventralis oralis anterior-ventralis oralis posterior border [the VO lead]) for the
39 egion along the ventral intermediate nucleus/ventralis oralis posterior nucleus border (4 mm anterior
40 DBS (one targeting the ventralis intermedius-ventralis oralis posterior nucleus border [the VIM lead]
41 nclude that the ventral intermediate nucleus/ventralis oralis posterior nucleus border and ventral in
42 ucleus region and for dystonic tremor in the ventralis oralis posterior nucleus region along the vent
43 lamic tracts, which primarily project to the ventralis oralis posterior nucleus region, significantly
44 l projections: reticularis (r.) dorsalis, r. ventralis pars alpha and beta, r. gigantocellularis, r.
45 active forms of both receptors reveals that ventralising signals from ALK-2* antagonise the dorsal m
46 in addition to regulating the production of ventralising signals, Foxg1 acts cell-autonomously in th
49 he locus coeruleus, the nucleus subcoeruleus ventralis, the nucleus of the solitary tract, and the ca
50 al, central, and lateral nucleus of the area ventralis [Vd, Vv, Vc, and Vl, respectively]), as well a
51 y ML lengthening due to musculus syringealis ventralis (VS) shortening is intrinsically constraint at