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1 ated during vocal production and conveyed to brainstem regions.
2 ma and neuropil of the deprived cortical and brainstem regions.
3  and subcortical gray matter, cerebellar and brainstem regions.
4 neurons in the superior colliculus and other brainstem regions.
5 ith varicosities were detected in almost all brainstem regions.
6  thalamic nuclei, cerebellum, and in several brainstem regions.
7 adly attenuated activity across cortical and brainstem regions.
8  [3H]BMZ (kappa) binding were analyzed in 21 brainstem regions.
9 dala, striatum, several thalamic nuclei, and brainstem regions.
10 se (1) each is located in nicotine-sensitive brainstem regions, (2) neurons containing each of these
11 sing pathways that originate in midbrain and brainstem regions and project onto the spinal cord, have
12 g., hippocampus and thalamus) and almost all brainstem regions; and (4) in sharp contrast to delta-op
13 dents identified the hypothalamus, vagus and brainstem regions as potential sites of action.
14 d ER alpha and ER beta neuronal densities in brainstem regions associated with cardiopulmonary regula
15 rimary motor (MI) cortex projects to several brainstem regions, but the relative strength of these pr
16                                            A brainstem region called the retrotrapezoid nucleus (RTN)
17 of this study was to determine which general brainstem regions contain interneurons that are critical
18                          Inactivation of the brainstem region containing ON and OFF cells also blocke
19                       Large lesions of other brainstem regions containing interneurons involved in re
20  the mesencephalic locomotor region (MLR), a brainstem region controlling locomotion in vertebrates.
21 cal role for this gene in the development of brainstem regions critical for conscious proprioception,
22 thalamus and project widely to forebrain and brainstem regions, densely innervating monoaminergic and
23 eginning by using functional MRI to identify brainstem regions differentially affected and resistant
24                         We show that diverse brainstem regions differentially target the 5HT neurons
25  In general, ER beta-positive neurons in the brainstem regions examined were less prevalent than ER a
26 expression in a dose-dependent manner in the brainstem regions examined.
27                                     Numerous brainstem regions express this transcript, notably monoa
28  comprised by somatosensory, cerebellar, and brainstem regions govern extinction behavior in preweanl
29 filed gene expression levels from postmortem brainstem regions, identifying a disease-related decreas
30 -expressing neurons specifically targeted to brainstem regions implicated in control of breathing, an
31 e early pathologic involvement of non-nigral brainstem regions in PD, as described by Braak.
32 eave the tract and grow into the surrounding brainstem regions in the elongation phase without any br
33 P2 function plays distinct roles in specific brainstem regions in the genesis of various aspects of a
34 -IA group, SERT were significantly higher in brainstem regions in the high-IA group (by 29.0% +/- 11.
35  terminalis, and the medial amygdala, and in brainstem regions including the lateral parabrachial nuc
36 le; 5) the neuropil of certain forebrain and brainstem regions, including nuclei of the song system;
37                                      Several brainstem regions, including nucleus rotundus, the media
38 (76 mg/kg; i.p.) c-Fos expression in several brainstem regions, including the area postrema, the nucl
39 biculum, and supramammillary nucleus, and in brainstem regions, including the lateral parabrachial nu
40 in the rostral ventromedial medulla (RVM), a brainstem region involved in modulation of nociception.
41 cts massively, via its central nucleus, into brainstem regions involved in alerting and in the genera
42 nin (5-HT) exerts excitatory effects in many brainstem regions involved in autonomic, somatic, motor,
43 suggest that the LPBN area is one of several brainstem regions involved in descending modulation of t
44 ques to examine Fos expression in limbic and brainstem regions involved in fear conditioning and in t
45 al drinking of 32% sucrose activated minimal brainstem regions involved in palatable taste, visceral
46 t and ventrolateral medulla as well as other brainstem regions involved in regulation of SND.
47 and ARNT2 mRNA were several hypothalamic and brainstem regions involved in the regulation of appetite
48 e observations suggest that the parabrachial brainstem region is the primary source of nitrergic fibe
49  the nucleus of the solitary tract and other brainstem regions known to regulate hemodynamic processe
50 s active during cataplexy and that innervate brainstem regions known to regulate motor tone.
51 central nucleus of the amygdala (CeA) target brainstem regions known to regulate muscle tone, we hypo
52 circuitry including amygdalar, thalamic, and brainstem regions, known in humans and other vertebrates
53 TC tract changes as well as abnormalities in brainstem regions linking cerebellar and basal ganglia m
54 nts of GABAA-receptor agonists into an upper brainstem region named the mesopontine tegmental anesthe
55 resulting unrestrained activity of Ang II in brainstem regions negatively impacts resting mean arteri
56  and arcuate nucleus of the hypothalamus and brainstem regions (nucleus of the solitary tract and A5
57 site is altered in the RVLM and other caudal brainstem regions of SHR, a quantitative densitometric a
58  demonstrate that PI3K in the cardiovascular brainstem regions of the SHR may be selectively involved
59 tive neurons were observed in caudal medulla brainstem regions, PACAP-containing nerve fibers were fo
60 ated by pacemaker-like neurons in 2 discrete brainstem regions: pre-Botzinger complex (preBotC) and p
61 st ascending auditory information from lower brainstem regions, receives prominent long-range inhibit
62 cerebral blood flow (in inner and cerebellum brainstem regions) remaining higher in the bolus surfact
63 s well as its connections with the phonatory brainstem regions responsible for the direct control of
64 eal size through descending inputs to caudal brainstem regions responsible for the motor pattern gene
65 including the caudate-putamen, amygdala, and brainstem regions such as the lateral parabrachial nucle
66 iceptive effect can be blocked by lesions of brainstem regions such as the periaqueductal gray (PAG)
67 eurons were present exclusively in the lower brainstem regions that contain the respiratory pattern g
68  in Fos expression in selected forebrain and brainstem regions that have been implicated in stress-in
69 uld directly trigger cataplexy by inhibiting brainstem regions that suppress muscle atonia.
70                                            A brainstem region, the paratrigeminal respiratory group (
71 tion are discussed briefly with reference to brainstem regions, the hypothalamus, and the forebrain.
72                                      In most brainstem regions, the intensity of hcrt-1 immunoreactiv
73 ll groups were observed in the forebrain and brainstem regions; these observations are compared with
74  reduced reward-learning signals in many non-brainstem regions: ventral striatum (VS), rostral and do
75 the embryonic week 10 specimen in which only brainstem regions were available for evaluation, trk imm

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