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1  was mediated by projections to the midbrain periaqueductal gray matter.
2 r cortices, nucleus accumbens, amygdala, and periaqueductal gray matter.
3 nuclei, central nucleus of the amygdala, and periaqueductal gray matter.
4   In addition, the ventrolateral part of the periaqueductal gray matter and gigantocellular reticular
5 reased gray matter in the midbrain including periaqueductal gray matter and nucleus cuneiformis, wher
6 e right amygdala and decreased activation in periaqueductal gray matter and the rostral anterior cing
7 y cortex, the anterior cingulate cortex, the periaqueductal gray matter, and other regions.
8 bnormal in hippocampus ( approximately 10%), periaqueductal gray matter ( approximately 13%), fimbria
9  the olfactory bulb ( approximately 10%) and periaqueductal gray matter ( approximately 16%).
10  rodents, that deep brain stimulation in the periaqueductal gray matter can rapidly and reversibly ma
11 cingulate cortex, caudate nuclei, brain stem periaqueductal gray matter, cerebellum, and occipital co
12 sterior hypothalamic nuclei), and brainstem (periaqueductal gray matter, dorsal and central superior
13  more modest, but labeling was strong in the periaqueductal gray matter, dorsal raphe nucleus, and la
14          Nitric oxide (NO) within the dorsal periaqueductal gray matter (dPAG) attenuated cardiovascu
15    Because chemokine administration into the periaqueductal gray matter inhibits opioid-induced analg
16 , followed by opioid administration into the periaqueductal gray matter of the brain results in an in
17 al cortex, the lateral hypothalamus, and the periaqueductal gray matter (PAG) are involved in these c
18 ase in the total phosphatase activity in the periaqueductal gray matter (PAG) from morphine-pelleted
19                                 The midbrain periaqueductal gray matter (PAG) has a critical role in
20                                          The periaqueductal gray matter (PAG) has been implicated in
21 ral or ventrolateral columns of the midbrain periaqueductal gray matter (PAG) in conscious animals pr
22 roinjection of dipyrone (metamizol) into the periaqueductal gray matter (PAG) in rats causes antinoci
23                                          The periaqueductal gray matter (PAG) is a major neuroanatomi
24                          Unlike the midbrain periaqueductal gray matter (PAG) or rostral ventromedial
25 orsal horn (DH) by brain regions such as the periaqueductal gray matter (PAG) plays a critical role i
26                                          The periaqueductal gray matter (PAG) projections to the intr
27                                          The periaqueductal gray matter (PAG) serves as the midbrain
28            The efferent projections from the periaqueductal gray matter (PAG) to the parabrachial nuc
29                                          The periaqueductal gray matter (PAG), a known modulator of s
30 nervate various targets, including thalamus, periaqueductal gray matter (PAG), and lateral parabrachi
31 nd the dorsolateral quadrant of the midbrain periaqueductal gray matter (PAG).
32 to the dorsolateral quadrant of the midbrain periaqueductal gray matter (PAG).
33 tions to lateral hypothalamus, dorsal raphe, periaqueductal gray matter, pericerulear region, rostrov
34 ial hypothalamic nuclei) and midbrain (viz., periaqueductal gray matter, precommissural nucleus, Edin
35 al scar, these fibers elongated in white and periaqueductal gray matter, reaching the farthest distan
36 rea, Edinger-Westphal nucleus, ventrolateral periaqueductal gray matter, reticular formation, peduncu
37 ing with EX was found in both colliculi, the periaqueductal gray matter, the parabrachial complex and
38 mygdala, prefrontal cortex, hippocampus, and periaqueductal gray matter to the control of conditioned
39 r ibotenic acid lesions of the ventrolateral periaqueductal gray matter (vlPAG) attenuated antinocice
40 -immunoreactive (TH-ir) cells in the ventral periaqueductal gray matter (vPAG) expressed Fos protein

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