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1 sponse (HCVR; a measure of respiratory CO(2) chemoreception).
2 2 to regulate breathing (central respiratory chemoreception).
3 hemenon which is not directly linked with O2 chemoreception.
4 s currently proposed for the mechanism of CB chemoreception.
5 ting towards an 'optimization' for efficient chemoreception.
6  new insights into the molecular genetics of chemoreception.
7 H(+) by a process referred to as respiratory chemoreception.
8 crucial for respiratory activity and central chemoreception.
9 phobic olfactory cues by a "tactile" form of chemoreception.
10 n of ASICs in the VLM contributes to central chemoreception.
11 lls as requisite determinants of respiratory chemoreception.
12 oth sexes, suggesting their putative role in chemoreception.
13 nergic signalling is a unique feature of RTN chemoreception.
14 previously identified neuromodulators of RTN chemoreception.
15 planation of their importance to respiratory chemoreception.
16 , including genes regulating ion balance and chemoreception.
17  retrotrapezoid nucleus (RTN) contributes to chemoreception.
18 ortance of medullary 5-HT neurons in central chemoreception.
19  been remarkably little study of its role in chemoreception.
20 etween the two competing theories of central chemoreception.
21 re involved in mechanoreception and possibly chemoreception.
22 P2 receptor signaling in central respiratory chemoreception.
23 ctions are consistent with a role in central chemoreception.
24 ugar alcohols and are related to sweet taste chemoreception.
25 a, thus playing an important role in central chemoreception.
26 K1R-ir neurons and processes are involved in chemoreception.
27 es" has added further interest in intranasal chemoreception.
28 al respiratory group, is involved in central chemoreception.
29 ntage of neurons not involved in respiratory chemoreception.
30 ness, (2) participate in central respiratory chemoreception, (3) stimulate breathing frequency, and (
31 he RTN and serotonergic cells to respiratory chemoreception also relies on many other types of eviden
32 gic (5-HT) neurons are implicated in central chemoreception and 5-HT abnormalities are present in man
33 nce factors or sensory enzymes involved with chemoreception and c-di-GMP signalling.
34                  Maturational differences in chemoreception and cerebral blood flow are evident at se
35 onse gene families such as those involved in chemoreception and detoxification.
36  breathing that are important in central CO2-chemoreception and for gating active expiration.
37 nt receptors) and pseudogene accumulation in chemoreception and P450 genes compared with A. mellifera
38 e adult brain has an important role in CO(2) chemoreception and reduced PHOX2B expression in CCHS bey
39 ressing parafacial neurons contribute to RTN chemoreception and respiratory activity.
40   The involvement of amphidial secretions in chemoreception and the behavioral and electrophysiologic
41 region (MRR) have been implicated in central chemoreception and the modulation of the ventilatory res
42   Thirdly, we argue for a key role for CO(2) chemoreception and the neural drive to breathe in the pa
43                               The defects in chemoreception and thermoregulation were exacerbated by
44 3- buffer is essential for the expression of chemoreception and to distinguish between pHi and pHo in
45 nteract with the surrounding environment via chemoreception, and in social insects such as ants, chem
46 neralized convulsive seizures impaired CO(2) chemoreception, and induced hypothermia, two effects rep
47 l tentacles serve contact- or short-distance chemoreception, and SSCs and the rhinophores function fo
48                                          For chemoreception, animals are believed to orient by compar
49 iew with Hany Dweck, who works on Drosophila chemoreception at Connecticut Agricultural Experiment St
50 1R)-expressing neurones that are involved in chemoreception at the retrotrapezoid nucleus are also pr
51 ese results broaden our understanding of the chemoreception basis of niche occupancy by blowflies.
52         These findings suggest that impaired chemoreception because of transient inhibition of seroto
53 ) may serve as molecular sensors for central chemoreception because they are highly expressed in mult
54 e the extent to which ATP contributes to RTN chemoreception both in vivo and in vitro, and whether pu
55 h were previously established in respiratory chemoreception, but do not innervate respiratory motor n
56 in the retrotrapezoid nucleus (RTN) supports chemoreception by a purinergic-dependent mechanism (Hawk
57 ignalling in respiratory control and central chemoreception by characterising the profile of the P2X
58  (the P box) in the periplasmic domain alter chemoreception by Nart and signaling by NarX similarly.
59 o which purinergic signalling contributes to chemoreception by RTN neurons is not clear and the mecha
60 spel the theory that ACh is required for RTN chemoreception by showing that ACh, similar to serotonin
61 th types, we evaluated their role in central chemoreception by specific cell killing.
62 in the integration of peripheral and central chemoreception (carotid bodies, chemoreceptor afferents,
63 l known about the sense of taste, or contact chemoreception, compared with other sensory modalities,
64 itivity, the notion that central respiratory chemoreception could rely on a few specialized neurons s
65 s of positive selection in genes involved in chemoreception, detoxification and digestion, and copy n
66 contribution of purinergic signalling to RTN chemoreception did not increase with temperature (22-35C
67 can be modified by a prior period of altered chemoreception during exercise.
68 li and/or cAMP may play an important role in chemoreception, especially in titrating the release of t
69 wn, we now show that comparable progesterone chemoreception exists in the invertebrate monogonont rot
70 naling, cuticular hydrocarbon synthesis, and chemoreception expanded in the ant ancestor, while many
71 luding tandem expansions of genes related to chemoreception, feeding, and digestion that possibly con
72 ception, and in social insects such as ants, chemoreception functions to mediate diverse behaviors in
73 CO(2), probably do not contribute to central chemoreception, given that they innervate sympathetic ef
74 s in pH to regulate breathing (i.e., central chemoreception) have remained incompletely understood, i
75 mbrane channel hypothesis of carotid body O2 chemoreception, hypoxia suppresses K+ currents leading t
76 n system participates importantly in central chemoreception in a vigilance-state- and diurnal-cycle-d
77 omeostasis in renal epithelial cells and CO2 chemoreception in brainstem neurons.
78                              Most studies on chemoreception in decapods have focused on the prominent
79 iration, photosynthesis in algae and plants, chemoreception in insects, and even global warming .
80 a common protein fold and assembly, used for chemoreception in insects, possibly by binding of a part
81     Here, we show that seizures impair CO(2) chemoreception in some epilepsy patients.
82 We consider recent progress in understanding chemoreception in the fly, including the identification
83  channels in postnatal maturation of hypoxic chemoreception in the rat carotid body.
84 did not support the redox hypothesis of O(2) chemoreception in the whole carotid body.
85 is known about the cells or mechanisms of O2 chemoreception in vertebrates other than mammals.
86 to define the cellular mechanisms of central chemoreception in vivo.
87  in the medulla are both involved in central chemoreception in vivo.
88 cleus (RTN) is a master regulator of central chemoreception, in particular, through direct sensation
89 re thought to function as important sites of chemoreception including the nucleus of the solitary tra
90                    In the RTN, mechanisms of chemoreception involve direct H(+)-mediated activation o
91                                              Chemoreception is essential for survival.
92                One of the early events in O2 chemoreception is inhibition of O2-sensitive K+ (KO2) ch
93                                       Insect chemoreception is mediated by a large and diverse superf
94 is that K+-O2 current is linked to events in chemoreception is not substantiated.
95                                              Chemoreception is the foundation of olfaction and taste,
96                                      Central chemoreception is the mechanism by which CO(2)/H(+) -sen
97                                      Central chemoreception is the mechanism by which the brain regul
98                          Central respiratory chemoreception is the mechanism by which the CNS maintai
99                                      Central chemoreception is the process whereby the brainstem sens
100                 A central question in insect chemoreception is whether signaling occurs via G-protein
101    Their contribution to central respiratory chemoreception may be behavior dependent or vary accordi
102                                          CO2 chemoreception may be mediated by the modulation of cert
103                                              Chemoreception, mediated by the odorant receptors on the
104        We also discuss how disruption of RTN chemoreception might contribute to breathing problems in
105  Females either rely less on 5-HT neurons in chemoreception or adapt more readily to the loss of 5-HT
106 d the rhinophores function for long-distance chemoreception or olfaction.
107                                              Chemoreception plays a crucial role in increasing mate e
108  understanding about the mechanisms of taste chemoreception, protein stabilization, etc.
109                          Central respiratory chemoreception refers to the component of this homeostat
110                                      Central chemoreception refers to the detection within the brain
111 s underlying the purinergic component of RTN chemoreception remains unknown.
112            Nevertheless, the field of oxygen chemoreception still presents the general observer with
113 itability or specifically related to central chemoreception, such as potassium channels.
114 antic confusion between chemosensitivity and chemoreception (the mechanism by which CO(2) or pH activ
115   A long-standing theory posits that central chemoreception, the CNS mechanism for CO(2) detection an
116                                      Central chemoreception, the highly sensitive ventilatory respons
117 ins neurons thought to contribute to central chemoreception, the process by which systemic hypercapni
118 n neurotransmitters such as ACh modulate RTN chemoreception, the results of the present study provide
119 he assumptions that underlie the distributed chemoreception theory to a critical analysis.
120                             The 'distributed chemoreception theory' attributes the central chemorefle
121 ences identified include a bias in bumblebee chemoreception towards gustation from olfaction, and str
122 host adaptation, including gene families for chemoreception, toxin and insecticide metabolism, cuticl
123  instead, cilia elongated and cilia-mediated chemoreception was abnormal.
124 ment of the control of breathing and central chemoreception, which may be pertinent to SIDS.
125 oid nucleus is a crucial hub for respiratory chemoreception within the brainstem.

 
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