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1 icance in two of the four nuclei (oralis and interpolaris).
2 nd 14% rostral to the obex (6% in subnucleus interpolaris, 4% in subnucleus oralis, and 4% in subnucl
4 of multiunit receptive fields in subnucleus interpolaris and caudalis were larger than previously ma
5 s-LI was induced in the trigeminal subnuclei interpolaris and caudalis, C1-2 dorsal horn, and other m
9 e distributed primarily in pars caudalis and interpolaris and provided inputs to the cochlear nucleus
11 ansition zone between subnuclei caudalis and interpolaris), and 14% rostral to the obex (6% in subnuc
14 abnormal barrelettes in the principalis and interpolaris brainstem nuclei and a complete absence of
15 neurons at the ventral trigeminal subnucleus interpolaris- caudalis (Vi/Vc) transition or the trigemi
16 rojections to RVM and PB from the trigeminal interpolaris-caudalis transition zone (Vi/Vc) in male an
18 the spinal trigeminal complex, the subnuclei interpolaris/caudalis (Vi/Vc) transition zone and the la
19 es have implicated a role for the trigeminal interpolaris/caudalis (Vi/Vc) transition zone in respons
20 ventral portion of the trigeminal subnuclei interpolaris/caudalis (Vi/Vc) transition zone, the perce
21 At the level of the trigeminal subnucleus interpolaris/caudalis (Vi/Vc) transition zone, there was
22 urons in the dorsal portion of the subnuclei interpolaris/caudalis transition zone at the level of th
23 Using the normal probability of observing an interpolaris cell with more than one trigeminal division
24 vibrissae receive only excitatory input from interpolaris cells that further project to the thalamus.
25 engthening of normally ineffective inputs to interpolaris cells, might contribute to the previously d
26 micropipettes, extracellular isolation of 37 interpolaris cells, with infraorbital receptive fields,
27 anomalies in trigeminal brainstem subnucleus interpolaris, including changes in normal receptive fiel
28 arating darkly stained patches in subnucleus interpolaris (juvenile tissue) and subnucleus caudalis (
29 llateral than maxillary axons; in oralis and interpolaris, mandibular fibers had fewer collaterals th
30 that (1) as expected, the rostral and caudal interpolaris neurons convey primarily whisking and touch
31 projects to the brain stem spinal trigeminal interpolaris nucleus, which contains whisker premotor ne
32 which includes the rostral spinal trigeminal interpolaris, posteromedial thalamic, and ventral zona i
33 ibuted throughout the ipsilateral subnucleus interpolaris, principal trigeminal nucleus, and intertri
35 es in both neurones in the spinal trigeminal interpolaris (Sp5I) nucleus and cardiac vagal neurones (
36 V nucleus principalis (PrV) and V subnucleus interpolaris (SpI) in the vinblastine-treated animals.
37 rns exist in the spinal trigeminal subnuclei interpolaris (SpVi) and subnuclei caudalis (SpVc) and th
38 trical stimulation of the trigeminal nucleus interpolaris (SpVi) evoked short latency responses (medi
39 hat lesions of the spinal trigeminal nucleus interpolaris (SpVi) significantly reduce the receptive f
40 predominantly from the principalis (PrV) and interpolaris (SpVi) subdivisions; 2) the incertal projec
41 oceptive touch signals in the oralis (SpVo), interpolaris (SpVi), and paratrigeminal (Pa5) brainstem
43 ngeal receptors the caudolateral part of the interpolaris subnucleus of the descending trigeminal tra
44 dorsal horn, subnucleus caudalis, subnucleus interpolaris, subnucleus oralis, and nucleus principalis
45 nal trigeminal subnucleus caudalis (SVc) and interpolaris (SVi), and the dorsal raphe nucleus exhibit