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1 llator located on the ventral surface of the medulla oblongata.
2 tes residing near the ventral surface of the medulla oblongata.
3 t express the ghrelin receptor (GHSR) in the medulla oblongata.
4 sterior tuberculum, the hypothalamus and the medulla oblongata.
5 slices containing the ventral surface of the medulla oblongata.
6 ependent ATP release from the surface of the medulla oblongata.
7 d periventricular and ventral regions of the medulla oblongata.
8 midline neurons and the caudal ventrolateral medulla oblongata.
9 llum, pyriform cortex, nucleus accumbens and medulla oblongata.
10 egions located on the ventral surface of the medulla oblongata.
11 to originate from neurons located within the medulla oblongata.
12 rom the nucleus of the solitary tract of the medulla oblongata.
13 s (DVN) and the nucleus ambiguus (NA) in the medulla oblongata.
14 ABAergic neurons) were mapped throughout the medulla oblongata.
15 ormed at about P2 in the central part of the medulla oblongata.
16 rons located in the parafacial region of the medulla oblongata.
17 hippocampus, substantia nigra, thalamus, and medulla oblongata.
18 e of the facial nerve nucleus in the rostral medulla oblongata.
19 developing dorsal and ventral region of the medulla oblongata.
20 ), a group of premotor neurons in the caudal medulla oblongata.
21 several types of respiratory neurons in the medulla oblongata.
22 r cell groups, especially those found in the medulla oblongata.
23 teralis, cerebellum, and motor nuclei of the medulla oblongata.
24 ventrolateral reticular nucleus (RVL) of the medulla oblongata.
25 d in the cortex, hypothalamus, striatum, and medulla oblongata.
26 owed clear entry into the choroid plexus and medulla oblongata.
27 could not be identified at the level of the medulla oblongata, all tracts were present bilaterally.
30 retroambiguus (NRA) is located in the caudal medulla oblongata and contains premotor neurons that pro
31 esponses in the cardiovascular nuclei of the medulla oblongata and increase neuronal excitability.
34 m the presence of lesions of motor tracts in medulla oblongata and spinal cord associated with other
40 ventrolateral reticular nucleus (RVL) of the medulla oblongata and sympathetic nerves and increased a
43 hibited increased levels of M2 mRNA in whole medulla oblongata, and an increase in the number of bind
45 lized (18)F-FDG uptake in the midbrain/pons, medulla oblongata, and cervical spinal cord as defined o
46 beled cells were not detected in the cortex, medulla oblongata, and spinal cord; few lightly labeled
47 ted to the neurotransmitter serotonin in the medulla oblongata, as these are the most robust patholog
48 existence of galanin immunoreactivity in the medulla oblongata, but a detailed characterization is la
49 1 and DNPI/VGLUT2 mRNAs were detected in the medulla oblongata by in situ hybridization, but only DNP
51 rrelated with the species mean volume of the medulla oblongata, cerebellum, and neocortical gray matt
52 emical techniques to demonstrate that in the medulla oblongata connexin 26 (Cx26) is preferentially e
53 expression of A(2A) receptors in regions of medulla oblongata containing GABAergic neurons, namely i
59 botropic glutamate receptors (mGluRs) in the medulla oblongata have been suggested to be involved in
60 d metabolic features were reported, although medulla oblongata hypermetabolism was associated with sh
61 Thus, the ghrelin receptor occurs in the medulla oblongata in 1) second-order sensory neurons pro
62 e [5-HT]) receptor binding in regions of the medulla oblongata involved in this control have been rep
64 ial arch, nasal processes, eyelid, midbrain, medulla oblongata, limbs, dorsal root ganglia and genita
65 of serotonin-1A receptors (5-HT(1A)R) in the medulla oblongata lowers sympathetic nerve discharge and
66 te (PCNG), striatum (STR), hippocampus (HC), medulla oblongata (MED) and anterior cingulate (ACNG) an
69 from the reproductive tract directly to the medulla oblongata of the brain, bypassing the spinal cor
72 e of lactate from the ventral surface of the medulla oblongata or cerebral cortex in brain slices of
74 a (CeA) projecting to the caudal dorsomedial medulla oblongata play a key role in the autonomic expre
75 and uniform in the caudal CNS (spinal cord, medulla oblongata, pons, and cerebellum) than in more ro
76 (5-hydroxytryptamine [5-HT]) neurons in the medulla oblongata project extensively to autonomic and r
77 ctures located on the ventral surface of the medulla oblongata rapidly release ATP, which acts locall
79 ta have shown that the rostral ventrolateral medulla oblongata (RVLM) plays an important role in toni
81 7) receptor are present in extracts from the medulla oblongata, spinal cord, and nodose ganglion.
82 usly defined a functional area in the caudal medulla oblongata that elicits an increase in arterial p
83 al nervous system, including a region of the medulla oblongata that is implicated in the control of r
84 on the cardio-respiratory oscillators in the medulla oblongata that modulate heart rate in phase with
85 ncluding the rhythm-generating region of the medulla oblongata - the preBotzinger complex (preBotC).
87 c acidergic (GABAergic) projections from the medulla oblongata to sympathetic preganglionic neurons.
88 ucleus Tractus Solitarii (NTS) region of the medulla oblongata, to which the Vagus nerves project, is
90 r (ML) that lines the ventral surface of the medulla oblongata (VMS) contains neurons thought to cont
92 ding the first linked to midbrain, pons, and medulla oblongata volumes, and map them to 305 genes.
93 glucose metabolism in the midbrain/pons and medulla oblongata was found in ALS/FTD patients (spinal-
94 function in the ventrolateral regions of the medulla oblongata was investigated in the anaesthetized
96 the distribution pattern of PAG axons in the medulla oblongata, WGA-HRP was injected into the PAG and
97 6, especially within the hippocampus and the medulla oblongata, when compared with non-COVID control
100 gic/catecholaminergic neurons located in the medulla oblongata, which may operate as a switchboard fo
101 ty (Kv3.1b-IR) was widespread throughout the medulla oblongata, with labelled neurones in the gracile
102 ons had similar distribution patterns in the medulla oblongata, with some areas exhibiting lighter la
103 tes in the hypothalamus, midbrain, pons, and medulla oblongata, with the major outflow terminating in