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1 fundus striatum, and nucleus of the lateral olfactory tract.
2 arbocyanine perchlorate (DiI) to the lateral olfactory tract.
3 itral cells, and in the fibers of the medial olfactory tracts.
4 thalamus, hippocampus, autonomic ganglia and olfactory tracts.
5 , posterior cortical, nucleus of the lateral olfactory tract, amygdalohippocampal area, and intercala
6 lation between white matter integrity in the olfactory tract and metabolic activity in olfactory proc
7 d when these tissues cause chemorepulsion of olfactory tract and spinal motor axons respectively, it
8 e Robo/Fc has no effect on chemorepulsion of olfactory tract and spinal motor axons when co-cultured
10 nondecussating pathways, such as the lateral olfactory tract and the habenulointerpeduncular tract.
13 rojected to either the medial or the lateral olfactory tract and, in general, the location of the cel
14 hock stimulation of afferent fibers (lateral olfactory tract) and association/commissural fibers evok
15 tion that courses, surrounding the accessory olfactory tract, and innervates several amygdaloid nucle
16 the larval and adult olfactory bulb, in the olfactory tract, and its targets in the telencephalon.
18 hypothalamic nucleus, nucleus of the lateral olfactory tract, and within substantia nigra pars compac
19 ronasal nuclei (bed nucleus of the accessory olfactory tract, BAOT, and medial amygdala, ME, replicat
20 aseline synaptic transmission in the lateral olfactory tract but not the associational afferents of t
21 amygdaloid nuclei (nucleus of the accessory olfactory tract, dorsolateral amygdala, external amygdal
23 regions, such as the nucleus of the lateral olfactory tract, exhibit astoundingly high Cbln2 express
25 fugal fibers, thalamocortical axons, lateral olfactory tract, hippocamposeptal projection, anterior c
27 organization of myelinated fibers in lateral olfactory tract in the anterior and posterior peduncle i
29 postsynaptic responses in the aPC to lateral olfactory tract input, shown to be enhanced at 24 h, are
30 hesized that MCI subjects would show loss of olfactory tract integrity and may have altered associati
31 ontrols, showed differential associations of olfactory tract integrity with medial temporal lobe and
32 bilateral transection of the rostral lateral olfactory tract (LOT) at the level of the anterior olfac
33 ifically, mitral cell axons form the lateral olfactory tract (LOT) by targeting lateral olfactory tra
34 eradish peroxidase (HRP) labeling of lateral olfactory tract (LOT) fibers in anterior piriform cortex
35 l olfactory tract (LOT) by targeting lateral olfactory tract (lot) guidepost cells in the piriform co
36 mulation of mitral cell axons in the lateral olfactory tract (LOT) resulted in excitation of pyramida
37 that interconnect the OB and PC: the lateral olfactory tract (LOT), which contains mitral cell axons
43 anterior commissure, but not in the lateral olfactory tract, mammillothalamic tract, or optic chiasm
44 hypothalamic nuclei, nucleus of the lateral olfactory tract, medial amygdala, hippocampal formation,
46 stimulation at 200 Hz applied to the lateral olfactory tract provides a substitute for the normal bac
47 r of mitotic nuclei threefold in the SVZ and olfactory tract, regions exhibiting persistent neurogene
48 tes, Slit causes chemorepulsion of embryonic olfactory tract, spinal motor, hippocampal and retinal g
49 erior commissure, the nucleus of the lateral olfactory tract, the anterior amygdaloid area, the poste
50 mygdaloid cortex, and nucleus of the lateral olfactory tract; these nuclei also contained variable nu
51 y the abolition of sniffing when the lateral olfactory tracts, were cut and the retention of rapid ar
52 ly unknown outer "shell" domain of the human olfactory tract, which express secretagogin, a cytosolic
53 association of fiber tract integrity in the olfactory tract with cortical glucose metabolism in subj
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