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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 ate a normalized, probabilistic atlas of the olfactory tracts.
6 , posterior cortical, nucleus of the lateral olfactory tract, amygdalohippocampal area, and intercala
7 ch the brain via systemic circulation or the olfactory tract and have been implicated in the risk of
8 lation between white matter integrity in the olfactory tract and metabolic activity in olfactory proc
9 d when these tissues cause chemorepulsion of olfactory tract and spinal motor axons respectively, it
10 e Robo/Fc has no effect on chemorepulsion of olfactory tract and spinal motor axons when co-cultured
11  from these tissues which cause repulsion of olfactory tract and spinal motor axons.
12 nondecussating pathways, such as the lateral olfactory tract and the habenulointerpeduncular tract.
13 ells by antidromic activation of the lateral olfactory tract and the posterior piriform cortex.
14 acts within the brain, including the lateral olfactory tract and the vomeronasal nerve.
15 rojected to either the medial or the lateral olfactory tract and, in general, the location of the cel
16 cterization of the connectivity of the human olfactory tracts and demonstrate an association between
17 link between the structural integrity of the olfactory tracts and odor perception.
18 hock stimulation of afferent fibers (lateral olfactory tract) and association/commissural fibers evok
19 tion that courses, surrounding the accessory olfactory tract, and innervates several amygdaloid nucle
20  the larval and adult olfactory bulb, in the olfactory tract, and its targets in the telencephalon.
21 olfactory bulb, the nucleus of the accessory olfactory tract, and the contralateral NS.
22 hypothalamic nucleus, nucleus of the lateral olfactory tract, and within substantia nigra pars compac
23 ronasal nuclei (bed nucleus of the accessory olfactory tract, BAOT, and medial amygdala, ME, replicat
24 aseline synaptic transmission in the lateral olfactory tract but not the associational afferents of t
25  amygdaloid nuclei (nucleus of the accessory olfactory tract, dorsolateral amygdala, external amygdal
26                   Stimulation of the lateral olfactory tract evoked an antidromic pulse followed by a
27  regions, such as the nucleus of the lateral olfactory tract, exhibit astoundingly high Cbln2 express
28            Voxelwise correlation analysis of olfactory tract FA values with (18)F-FDG PET images was
29 ance imaging (dMRI) to reconstruct the human olfactory tracts has been prevented by susceptibility an
30 fugal fibers, thalamocortical axons, lateral olfactory tract, hippocamposeptal projection, anterior c
31 ositive neurons selectively decreases in the olfactory tract in Alzheimer's disease.
32 organization of myelinated fibers in lateral olfactory tract in the anterior and posterior peduncle i
33 image distortions and characterize the human olfactory tracts in vivo We collected high-resolution dM
34  is congruent with the maturation of lateral olfactory tract input in rat pups.
35 postsynaptic responses in the aPC to lateral olfactory tract input, shown to be enhanced at 24 h, are
36 hesized that MCI subjects would show loss of olfactory tract integrity and may have altered associati
37 ontrols, showed differential associations of olfactory tract integrity with medial temporal lobe and
38 bilateral transection of the rostral lateral olfactory tract (LOT) at the level of the anterior olfac
39 ifically, mitral cell axons form the lateral olfactory tract (LOT) by targeting lateral olfactory tra
40 eradish peroxidase (HRP) labeling of lateral olfactory tract (LOT) fibers in anterior piriform cortex
41 l olfactory tract (LOT) by targeting lateral olfactory tract (lot) guidepost cells in the piriform co
42 m the olfactory bulb carried via the lateral olfactory tract (LOT) is 'hardwired.' Here, we revisit t
43  (OB) to piriform cortex through the lateral olfactory tract (LOT) relies on synchronized arrival of
44 mulation of mitral cell axons in the lateral olfactory tract (LOT) resulted in excitation of pyramida
45  inputs and sensory signals from the lateral olfactory tract (LOT) revealed that simultaneous LEC and
46 that interconnect the OB and PC: the lateral olfactory tract (LOT), which contains mitral cell axons
47                                      Lateral olfactory tract (LOT)-evoked responses were recorded in
48 t form an axonal bundle known as the lateral olfactory tract (LOT).
49 following dextran injection into the lateral olfactory tract (LOT).
50 lowing antidromic stimulation of the lateral olfactory tract (LOT).
51 ted by antidromic stimulation of the lateral olfactory tract (LOT).
52  anterior commissure, but not in the lateral olfactory tract, mammillothalamic tract, or optic chiasm
53                   Importantly, we found that olfactory tract MD negatively correlated with odor discr
54  hypothalamic nuclei, nucleus of the lateral olfactory tract, medial amygdala, hippocampal formation,
55                   The nucleus of the lateral olfactory tract (nLOT) is a cortical nucleus of the pall
56   The pathway via the nucleus of the lateral olfactory tract (NLOT) that receives input from olfactor
57                                          The olfactory tracts project from the olfactory bulb along t
58 stimulation at 200 Hz applied to the lateral olfactory tract provides a substitute for the normal bac
59 r of mitotic nuclei threefold in the SVZ and olfactory tract, regions exhibiting persistent neurogene
60 tes, Slit causes chemorepulsion of embryonic olfactory tract, spinal motor, hippocampal and retinal g
61 on of the cortical connectivity of the three olfactory tract striae in the human brain, using diffusi
62 ated a normalized probabilistic atlas of the olfactory tracts that may be used in future research to
63 erior commissure, the nucleus of the lateral olfactory tract, the anterior amygdaloid area, the poste
64 mygdaloid cortex, and nucleus of the lateral olfactory tract; these nuclei also contained variable nu
65 olfactory bulb and then sent via the lateral olfactory tract to a series of olfactory cortical areas.
66 y the abolition of sniffing when the lateral olfactory tracts, were cut and the retention of rapid ar
67 ly unknown outer "shell" domain of the human olfactory tract, which express secretagogin, a cytosolic
68  association of fiber tract integrity in the olfactory tract with cortical glucose metabolism in subj