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1 rom this laboratory showed that sprouting of serotoninergic (5-HT) axons in the hamster's superior co
2 in a significant increase in the density of serotoninergic (5-HT) fibers in the superficial layers o
4 of the dendrites that there is indeed both a serotoninergic and noradrenergic innervation of gamma-mo
6 eled fibers were unequivocally identified as serotoninergic and originating from one of the labeled n
9 rom this laboratory showed that sprouting of serotoninergic axons in the hamster's superior colliculu
11 to the lateral subdivision of the IPN, high serotoninergic binding was localized to the dorsal IPN,
12 abel serotoninergic fibers and boutons, 1048 serotoninergic boutons were observed in close contact wi
13 level of the orbitofrontal cortex (OFC) with serotoninergic, but not dopaminergic, integrity being im
14 ivity of anti-52-kD SSA/Ro antibodies with a serotoninergic cardiac receptor, 5-hydroxytryptamine (HT
15 active TH-ir cells but did not injure nearby serotoninergic cells, increased total daily sleep by app
18 em, where they provided terminals in the the serotoninergic dorsal and median raphe nuclei, and the c
20 airway in waking, and that in sleep, reduced serotoninergic drive plays a significant role in upper a
22 -hydroxytryptamine-immunoreactivity to label serotoninergic fibers and boutons, 1048 serotoninergic b
24 ergic-andrenergic, glutaminergic-GABAnergic, serotoninergic, histaminergic, and cholinergic systems.
25 We hypothesized that in OSAHS, excitatory serotoninergic influences are important for maintaining
28 rted small responses in humans with OSAHS to serotoninergics may relate, in part, to study design and
30 e control monkeys and monkeys with selective serotoninergic medial caudate depletions, dopamine-deple
33 nition task in rats to study the role of the serotoninergic modulation in the medial PFC (mPFC) in me
34 nsiderable body of literature indicates that serotoninergic neurons affect diaphragm activity both th
35 argeted the cell bodies and dendrites of DRN serotoninergic neurons and LC noradrenergic neurons but
38 function of VGLUT3 in acetylcholinergic and serotoninergic neurons has been elucidated, the role of
43 tem respiratory groups, the locations of the serotoninergic neurons that modulate breathing have not
45 1A autoreceptors reduces the excitability of serotoninergic neurons, which decreases serotonin releas
47 rammed cell death in the sister cells of the serotoninergic neurosecretory motor (NSM) neurons, and f
48 erotonin (5-HT) transporter (SERT) regulates serotoninergic neurotransmission by clearing 5-HT releas
49 ministration in nonhuman primates influences serotoninergic neurotransmission via at least two ways:
52 cholinergic or monoaminergic (noradrenergic, serotoninergic or dopaminergic) nuclei in the brainstem
53 c denervation although not with differential serotoninergic or nigrostriatal dopaminergic denervation
54 this study compared the effects of selective serotoninergic or selective dopaminergic depletions of t
56 to synapse, cell adhesion, glutamatergic and serotoninergic pathways, both confirming findings of pre
57 rsal cochlear nucleus, we concluded that the serotoninergic projection pattern to the cochlear nucleu
59 habenula (LHb) is bilaterally connected with serotoninergic raphe nuclei, and expresses high density
60 eus, histaminergic tuberomammillary nucleus, serotoninergic raphe nucleus, and dopaminergic ventral t
61 ogy of depression after DD, including NA-LC, serotoninergic-raphe nuclei and dopaminergic-ventral teg
66 hether genetic variation in genes across the serotoninergic system is associated with chronic widespr
70 s indicate the causal involvement of reduced serotoninergic transmission in the emergence of compulsi
72 esting the effectiveness of a combination of serotoninergics, trazodone, and L-tryptophan, in our ani
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