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1 egion are most medial and include the median pontine nucleus.
2  hippocampus, dentate gyrus, red nucleus and pontine nucleus.
3 dial habenular nucleus, thalamic nucleus and pontine nucleus.
4 bic lip together with neurons of the lateral pontine nucleus.
5  lemniscus, inferior colliculus, and lateral pontine nucleus.
6 om the medial central nucleus to the basilar pontine nucleus.
7  tegmentum and can be traced into the medial pontine nucleus.
8 a (LHb), ventral tegmental area, and lateral pontine nucleus.
9 ebellum (the mossy fibers emanating from the pontine nucleus and climbing fibers originating from the
10 nce in the frequency of NCIs in the putamen, pontine nucleus and inferior olivary nucleus between the
11  the limbs and body to the thalamus, cortex, pontine nucleus, and cerebellum.
12 e tracing experiments identified the basilar pontine nucleus at the confluence of outputs from CeA th
13  nuclei (e.g., habenula, supraoptic nucleus, pontine nucleus) contained pronounced levels of GCP II m
14 -/-) mice and found that they have disrupted pontine nucleus development.
15 ral pontine nucleus, whereas inactivation of pontine nucleus had little effect on similar activity in
16 st ages, visual cortical axons innervate the pontine nucleus in regions specific to their adult proje
17                              In mammals, the pontine nucleus locus ceruleus (LC) is the sole source o
18 b (MOB) receives a dense projection from the pontine nucleus locus coeruleus (LC), the largest collec
19       Neurons in the piriform cortex and the pontine nucleus locus coeruleus express elevated levels
20 r cervical ganglion (SCG), as well as in the pontine nucleus locus coeruleus, and the sympathetic inn
21 oliation defects, motor impairments, partial pontine nucleus migration defects, cochlear hair cell de
22 c nuclei, superior colliculus, zona incerta, pontine nucleus, multiple other brainstem areas, and the
23 olfactory bulb, red nucleus, facial nucleus, pontine nucleus, oculomotor nucleus, substantia nigra, d
24 on of cerebellar deep nuclei and the lateral pontine nucleus on classical eyeblink conditioning with
25  biotinylated dextran amine into the lateral pontine nucleus (PL), and led to extensive retrograde la
26  nucleus (IPN) of the cerebellum and basilar pontine nucleus (PN) during different phases of training
27                  Inactivation of the lateral pontine nucleus prevented only the acquisition and reten
28 al and medial geniculate bodies, the basilar pontine nucleus, the horizontal limb of the diagonal ban
29 ing-induced neuronal activity in the lateral pontine nucleus was most likely driven by the cerebellar
30 ing-related neuronal activity in the lateral pontine nucleus, whereas inactivation of pontine nucleus

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