戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 ocated on the ventral surface of the medulla oblongata.
2 ding near the ventral surface of the medulla oblongata.
3 s the ghrelin receptor (GHSR) in the medulla oblongata.
4 tuberculum, the hypothalamus and the medulla oblongata.
5 ontaining the ventral surface of the medulla oblongata.
6  ATP release from the surface of the medulla oblongata.
7 ntricular and ventral regions of the medulla oblongata.
8 neurons and the caudal ventrolateral medulla oblongata.
9 riform cortex, nucleus accumbens and medulla oblongata.
10 ocated on the ventral surface of the medulla oblongata.
11 nate from neurons located within the medulla oblongata.
12 nucleus of the solitary tract of the medulla oblongata.
13 and the nucleus ambiguus (NA) in the medulla oblongata.
14  neurons) were mapped throughout the medulla oblongata.
15  about P2 in the central part of the medulla oblongata.
16 ated in the parafacial region of the medulla oblongata.
17 pus, substantia nigra, thalamus, and medulla oblongata.
18  facial nerve nucleus in the rostral medulla oblongata.
19 ing dorsal and ventral region of the medulla oblongata.
20 up of premotor neurons in the caudal medulla oblongata.
21  types of respiratory neurons in the medulla oblongata.
22 roups, especially those found in the medulla oblongata.
23  cerebellum, and motor nuclei of the medulla oblongata.
24 teral reticular nucleus (RVL) of the medulla oblongata.
25  cortex, hypothalamus, striatum, and medulla oblongata.
26 ar entry into the choroid plexus and medulla oblongata.
27 ot be identified at the level of the medulla oblongata, all tracts were present bilaterally.
28                However, in the upper medulla oblongata alpha2 mRNA was expressed in several large neu
29 i cells and large motoneurons in the medulla oblongata and cervical spinal cord.
30 iguus (NRA) is located in the caudal medulla oblongata and contains premotor neurons that project to
31  in the cardiovascular nuclei of the medulla oblongata and increase neuronal excitability.
32                               In the medulla oblongata and pons, we detected Hoxa5 expression in many
33  the main respiratory centers of the medulla oblongata and pons.
34 esence of lesions of motor tracts in medulla oblongata and spinal cord associated with other lesions
35 ribution of the Kv3.3 subunit in the medulla oblongata and spinal cord of rats.
36 ibitory synaptic transmission in the medulla oblongata and spinal cord.
37 ar nuclei, and subpopulations of the medulla oblongata and spinal cord.
38 d in numerous neurons throughout the medulla oblongata and spinal cord.
39 e highest by a factor of four in the medulla oblongata and spinal cord.
40 teral reticular nucleus (RVL) of the medulla oblongata and sympathetic nerves and increased arterial
41 bserved in the subpial region of the medulla oblongata and the spinal cord.
42   The brainstem (midbrain, pons, and medulla oblongata) and cerebellum (diencephalic prosomere 1 thro
43 increased levels of M2 mRNA in whole medulla oblongata, and an increase in the number of binding site
44 erent brain regions, including pons, medulla oblongata, and cerebellum.
45 8)F-FDG uptake in the midbrain/pons, medulla oblongata, and cervical spinal cord as defined on the in
46 lls were not detected in the cortex, medulla oblongata, and spinal cord; few lightly labeled cells we
47 he neurotransmitter serotonin in the medulla oblongata, as these are the most robust pathologic findi
48 e of galanin immunoreactivity in the medulla oblongata, but a detailed characterization is lacking.
49 PI/VGLUT2 mRNAs were detected in the medulla oblongata by in situ hybridization, but only DNPI/VGLUT2
50 e prefrontal cortex rostrally to the medulla oblongata caudally.
51  with the species mean volume of the medulla oblongata, cerebellum, and neocortical gray matter, we c
52 echniques to demonstrate that in the medulla oblongata connexin 26 (Cx26) is preferentially expressed
53 ion of A(2A) receptors in regions of medulla oblongata containing GABAergic neurons, namely in the ve
54 e show that the A1/C1 neurons of the medulla oblongata drive AVP neuron activation in response to ins
55    ATP released in the ventrolateral medulla oblongata during hypoxia attenuates the secondary depres
56                               In the medulla oblongata, GAL-ir neurons appear in the anterodorsal and
57   The ventral surface of the rostral medulla oblongata has been suspected since the 1960s to harbor c
58                                  The medulla oblongata has previously been implicated in this type of
59  glutamate receptors (mGluRs) in the medulla oblongata have been suggested to be involved in the regu
60 lic features were reported, although medulla oblongata hypermetabolism was associated with shortened
61 , the ghrelin receptor occurs in the medulla oblongata in 1) second-order sensory neurons processing
62 ) receptor binding in regions of the medulla oblongata involved in this control have been reported in
63                               In the medulla oblongata, labelled cell bodies were numerous in the spi
64 , nasal processes, eyelid, midbrain, medulla oblongata, limbs, dorsal root ganglia and genital tuberc
65 onin-1A receptors (5-HT(1A)R) in the medulla oblongata lowers sympathetic nerve discharge and blood p
66 ), striatum (STR), hippocampus (HC), medulla oblongata (MED) and anterior cingulate (ACNG) and five p
67           C1 neurons, located in the medulla oblongata, mediate adaptive autonomic responses to physi
68 rhythmically active preBotC from the medulla oblongata of neonatal mice.
69 e reproductive tract directly to the medulla oblongata of the brain, bypassing the spinal cord.
70               Ventral regions of the medulla oblongata of the brainstem are populated by astrocytes s
71 tected in the olfactory zone and the medulla oblongata of the human brain.
72 tate from the ventral surface of the medulla oblongata or cerebral cortex in brain slices of MeCP2-kn
73 tructures (e.g. hypothalamus) to the medulla oblongata, particularly the cNTS.
74 projecting to the caudal dorsomedial medulla oblongata play a key role in the autonomic expression of
75 form in the caudal CNS (spinal cord, medulla oblongata, pons, and cerebellum) than in more rostral ar
76 oxytryptamine [5-HT]) neurons in the medulla oblongata project extensively to autonomic and respirato
77 ocated on the ventral surface of the medulla oblongata rapidly release ATP, which acts locally within
78 ion (within the carotid body and the medulla oblongata, respectively).
79 shown that the rostral ventrolateral medulla oblongata (RVLM) plays an important role in tonic blood
80 onverge in the rostral ventrolateral medulla oblongata (RVLM).
81 tor are present in extracts from the medulla oblongata, spinal cord, and nodose ganglion.
82 ined a functional area in the caudal medulla oblongata that elicits an increase in arterial pressure
83 us system, including a region of the medulla oblongata that is implicated in the control of respirati
84 ardio-respiratory oscillators in the medulla oblongata that modulate heart rate in phase with respira
85  the rhythm-generating region of the medulla oblongata - the preBotzinger complex (preBotC).
86                               In the medulla oblongata, the retrotrapezoid nucleus (RTN) and rostral
87 gic (GABAergic) projections from the medulla oblongata to sympathetic preganglionic neurons.
88 ractus Solitarii (NTS) region of the medulla oblongata, to which the Vagus nerves project, is activat
89                    The ventrolateral medulla oblongata (VLM) of the brainstem contains neurochemicall
90 hat lines the ventral surface of the medulla oblongata (VMS) contains neurons thought to contribute t
91 ocated at the ventral surface of the medulla oblongata (VMS).
92  first linked to midbrain, pons, and medulla oblongata volumes, and map them to 305 genes.
93  metabolism in the midbrain/pons and medulla oblongata was found in ALS/FTD patients (spinal-ALS and
94  in the ventrolateral regions of the medulla oblongata was investigated in the anaesthetized rat.
95 idths of the third ventricle and the medulla oblongata were used as linear atrophy measures.
96 ribution pattern of PAG axons in the medulla oblongata, WGA-HRP was injected into the PAG and adjacen
97 ially within the hippocampus and the medulla oblongata, when compared with non-COVID control hamsters
98                         Sites in the medulla oblongata where bombesin acts to suppress gastric acid s
99                          The midline medulla oblongata, which includes the nucleus raphe obscurus, ra
100 cholaminergic neurons located in the medulla oblongata, which may operate as a switchboard for differ
101 1b-IR) was widespread throughout the medulla oblongata, with labelled neurones in the gracile, cuneat
102 similar distribution patterns in the medulla oblongata, with some areas exhibiting lighter labeling f
103 he hypothalamus, midbrain, pons, and medulla oblongata, with the major outflow terminating in bulbosp

 
Page Top