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1 2+)-activated Cl(-) channels, generating the receptor potential.
4 or example, the vanilloid receptor transient receptor potential 3 (TRPV3), which has been implicated
5 iotensin II (Ang II) via canonical transient receptor potential 6 (TRPC6) channels caused increased i
6 found that inhibition of canonical transient receptor potential 6 (TRPC6) channels facilitated contra
8 lators of cytosolic Ca(2+) levels, transient receptor potential A1 (TRPA1) and ryanodine receptor (Ry
10 t previous studies have found that transient receptor potential A1 (TRPA1) gene deletion blocks CQ-in
11 ne novel therapeutic target is the Transient Receptor Potential A1 channel (TRPA1), an ion channel th
12 Lowering R(in) will reduce the hair cells receptor potential and presumably moderate the systems s
13 nsation, basolateral ion channels that shape receptor potential, and synaptic contacts for conveying
14 that activation of the ion channel transient receptor potential ankyrin 1 (TRPA1) alone indeed suffic
20 dehydrogenase (ADH) or deletion of transient receptor potential ankyrin 1 (TRPA1), a sensor for oxida
23 activate EECs through the receptor transient receptor potential ankyrin A1 (Trpa1) and increase intes
24 These noxious anesthetics activate transient receptor potential ankyrin repeat 1 (TRPA1), a major noc
25 anesthetics inhibit agonist-evoked transient receptor potential ankyrin type 1 (TRPA1) activity and i
27 smoke particulate matter and other transient receptor potential ankyrin-1 (TRPA1) and transient recep
29 vagus, and this was inhibited by a transient receptor potential ankyrin-1 antagonist and the antioxid
30 uction, which is known to activate transient receptor potential ankyrin-1 on nociceptive C-fibers.
35 selective Orai1 and members of the transient receptor potential canonical (TRPC) channels, which are
37 bone marrow cells deficient in the Transient Receptor Potential Canonical 3 (TRPC3) channel have redu
42 , and synaptopodin and to enhanced transient receptor potential canonical 6 (TRPC6) channel expressio
43 e have recently discovered a novel transient receptor potential canonical 6 (TRPC6)-mediated intracel
46 f the nonselective cation channel, transient receptor potential canonical channel 6 (Trpc6), in isola
49 tects the heart by down-regulating transient receptor potential canonical isoform 6 (TRPC6)-mediated
50 revious work, we hypothesized that transient receptor potential canonical type 3 (TRPC3) channels are
53 down-regulating calcium-permeable transient receptor potential canonical type isoform 6 (TRPC6) chan
54 "M-type") K(+) channels and TRPC (transient receptor potential, "canonical") cation channels are cou
55 ons that include M channels, TRPC (transient receptor potential, "canonical") cation channels, and po
56 Moreover, we demonstrated that transient receptor potential cation channel (TRP)-A1 was the ion c
57 orters, aquaporin 5 (AQP5) and the transient receptor potential cation channel (TRPV4), was investiga
59 increased calcium entry though the transient receptor potential cation channel 6 (TRPC6), causing hyp
60 unction mouse models, we show that transient receptor potential cation channel C3 (TRPC3) controls th
63 mRNA expression of PGP9.5; TRPV1; transient receptor potential cation channel subfamily A, receptor
64 ecretion through coupling with the transient receptor potential cation channel subfamily C 3 (TRPC3).
66 expression via the Ca(2+) channel, transient receptor potential cation channel subfamily C member 6 (
67 2 (NCX2) works in conjunction with transient receptor potential cation channel subfamily M member 4 (
69 uorescent protein (EGFPf) from the transient receptor potential cation channel subfamily M member 8 (
70 ygen species (ROS), which acted on transient receptor potential cation channel subfamily M member 8 (
71 receptor neurons expressing TRPM8 (transient receptor potential cation channel subfamily M member 8).
72 mily A, receptor 1 (TRPA1); TRPV4; transient receptor potential cation channel subfamily M, member 8
73 from only unmyelinated afferents [transient receptor potential cation channel subfamily V member 1 (
74 re organized exclusively as either transient receptor potential cation channel subfamily V member 1 (
75 n (a vanilloid) that activates the transient receptor potential cation channel subfamily V member 1 (
76 iceptor) or also exhibiting TRPV1 (transient receptor potential cation channel subfamily V member 1)
77 y following calcium influx through transient receptor potential cation channel subfamily V member 2 c
79 s (IR) is based on ablation of the transient receptor potential cation channel subfamily V, receptor
81 o the thermosensors, including the transient receptor potential cation channel V1 expressed in the no
83 showed increased expression of the transient receptor potential cation channel, subfamily C, member 6
84 ve been linked to mutations in the transient receptor potential cation channel, subfamily C, member 6
86 independently of Piezo1 by TRPV4 (transient receptor potential cation channel, subfamily V, member 4
87 66Shc restricted the activation of transient receptor potential cation channels to attenuate cytosoli
88 (VSMCs), stimulation of canonical transient receptor potential channel 1 (TRPC1) protein-based store
89 tion of SOCs composed of canonical transient receptor potential channel 1 (TRPC1) proteins requires G
90 nnels (SOCs) composed of canonical transient receptor potential channel 1 (TRPC1) subunits mediates C
91 ion of Ca(2+) -permeable canonical transient receptor potential channel 1 (TRPC1)-based store-operate
92 (SPHK1) in the mechanism by which transient receptor potential channel 1 (Trpc1)-mediated Ca(2+) ent
98 least partly mediated through the transient receptor potential channel 6, which has been implicated
100 Here, we identified mucolipin 1 (transient receptor potential channel mucolipin 1 [TRPML1], also kn
101 es, or TRPP-PKD complexes, made of transient receptor potential channel polycystin (TRPP) and polycys
103 and menthol-activated ion channel transient receptor potential channel subfamily M member 8 (TRPM8)
104 omotes expression of the canonical transient receptor potential channel subunit TRPC4 in normal and t
105 nts in transduction channels, like transient receptor potential channel TRPA1 and voltage-gated sodiu
106 Here, we identify the canonical transient receptor potential channel Trpc5 as an essential require
107 at Pkd2p, a putative force-sensing transient receptor potential channel, localizes to the cleavage fu
108 ctivates the extreme cold receptor transient receptor potential channel, subfamily A, member 1 and ma
109 as in vitro confirmed the role of transient receptor potential channels (TRPA1 and TRPV1) as OxPAPC
111 voltage-gated Ca(2+) channels and transient receptor potential channels in addition to release from
112 ivation mechanism of the classical transient receptor potential channels TRPC4 and -5 via the Gq/11 p
113 include integrins, Piezo channels, transient receptor potential channels, and nonselective ion channe
117 , a group of ion channels from the transient receptor potential family, play important functions in p
118 base and submillisecond encoding of membrane receptor potential fluctuations in the apex for precise
123 Animal studies have suggested that transient receptor potential ion channels and G-protein coupled re
126 Y POINTS: Endothelial cells employ transient receptor potential isoform 4 (TRPV4) channels to sense a
127 meability assays, we show that the transient receptor potential isoform 4 (TRPV4) plays a major role
129 R-211, which is expressed from the transient receptor potential melastatin 1 intronic region, regulat
133 NvTRPM2 (Nematostella vectensis Transient Receptor Potential Melastatin 2), the species variant of
140 ogical and molecular inhibition of transient receptor potential melastatin 7 (TRPM7) reduces store-op
141 ozygous, nonsynonymous variants in transient receptor potential melastatin 7 (TRPM7), a ubiquitously
142 The cold- and menthol-sensitive transient receptor potential melastatin 8 (TRPM8) channel is impor
145 of the cold- and menthol-sensitive transient receptor potential melastatin 8 (TRPM8) ion channels.
146 d testosterone signaling receptor, Transient Receptor Potential Melastatin 8 (TRPM8), regulates dimor
147 n potentials and exhibited robust, transient receptor potential melastatin 8 (TRPM8)-dependent discha
148 receptor potential vanilloid 1 and transient receptor potential melastatin 8 in sensory neurons and c
149 receptor potential vanilloid 1 and transient receptor potential melastatin 8) in primary sensory neur
154 novalent cation current carried by transient receptor potential melastatin subfamily 4 channels via t
160 e lysosomal Ca(2+) release channel transient receptor potential mucolipin 1 (TRPML1) but not the lyso
165 volvement of endolysosome-resident transient receptor potential mucolipin 1 channel (TRPML1) and the
168 buprofen-treated worms and a TRPV (transient receptor potential) mutant, and we show that the percept
169 differ with stimulus modality and will shape receptor potentials of different hair cell types based o
170 verall structure of many classical transient receptor potential proteins (TRPC), including human and
172 anges in membrane potentials, the so called "receptor potentials." Ribbon synapses between IHCs and a
173 We present a model that relates the early receptor potential to these deformations based on the vo
174 oxia via the sensor cation channel transient receptor potential (TRP) A1 but, unlike multimodal senso
175 is study investigated the roles of transient receptor potential (TRP) ankyrin-1 (TRPA1) and TRP vanil
176 merly TRPP2) is a calcium-permeant Transient Receptor Potential (TRP) cation channel expressed primar
177 f the peripheral irritant receptor transient receptor potential (TRP) cation channel member A1 (TRPA1
181 esolution cryo-EM structure of the transient receptor potential (TRP) channel crTRP1 from the alga Ch
182 and in vivo electrophysiology that transient receptor potential (TRP) channel dephosphorylation at a
183 Rs modulate several members of the transient receptor potential (TRP) channel family of nonselective
186 ISPR/Cas9 knockout to identify the Transient Receptor Potential (TRP) channel subfamily M (Trpm) as a
187 e that PZQ activates a schistosome transient receptor potential (TRP) channel, christened SmTRPM(PZQ)
192 before the origin of bilateria and transient receptor potential (TRP) channels before the origin of a
194 favour of dim light depends on the transient receptor potential (TRP) channels dTRPA1 and Pyrexia, an
196 e activation of several functional transient receptor potential (TRP) channels in live cells and in r
199 exploit these properties by using transient receptor potential (TRP) channels to activate or ablate
200 OINTS: Retinal cells use vanilloid transient receptor potential (TRP) channels to integrate light-evo
205 ey modulate the expression of some transient receptor potential (TRP) family members, yet their role
209 phorylation of the light-activated transient receptor potential (TRP) ion channel at S936 is a fast,
211 he ion permeation mechanism in the transient receptor potential (TRP) ion channel family is currently
214 ncluding agonists of nocisensitive transient receptor potential (TRP) ion channels on somatosensory f
215 t stimulates cation influx through transient receptor potential (TRP) melastatin 4 (TRPM4) channels t
219 ion channels in kidney cells, the transient receptor potential (TRP) superfamily of proteins plays i
221 in vitro myogenesis by stimulating transient receptor potential (TRP)-C1-mediated calcium entry and d
222 sensory neurogenic mechanisms for transient receptor potential (TRP)V1, TRPA1, and neuropeptides (su
224 (2+) entry (SOCE), while classical transient receptor potential (TRPC) channel mediate receptor-opera
226 members of the melastatin-related transient receptor potential (TRPM) subfamily of ion channels.
227 the ligand-gated calcium channels transient receptor potential V1 and M8 (transient receptor potenti
229 ed Caco-2 resistance by 20-30% via transient receptor potential vanilloid (TRPV)-1 and peroxisome pro
231 responses to inhaled capsaicin, a transient receptor potential vanilloid 1 (TRPV1) agonist, are char
232 ibition requires the expression of transient receptor potential vanilloid 1 (TRPV1) and TRPN-like cha
233 The capsaicin- and heat-activated transient receptor potential vanilloid 1 (TRPV1) channel contribut
236 acellularly located cation channel transient receptor potential vanilloid 1 (TRPV1) in endothelial ce
240 ed glutamate release was absent in transient receptor potential vanilloid 1 (TRPV1) KO mice and preve
242 asthmakines involves a PKCepsilon-transient receptor potential vanilloid 1 (TRPV1) signalling mechan
243 of the heat-activated ion channel transient receptor potential vanilloid 1 (TRPV1) through lipids is
244 roduces burning pain by activating transient receptor potential vanilloid 1 (TRPV1), a Ca(2+)-permeab
245 of a thermoregulatory ion channel, transient receptor potential vanilloid 1 (TRPV1), by dihydrocapsai
246 KCepsilon-dependent stimulation of transient receptor potential vanilloid 1 (TRPV1), likely via TRPV1
247 lipid that potently activates the transient receptor potential vanilloid 1 (TRPV1), which mediates p
250 the activation of the ion channels transient receptor potential vanilloid 1 and transient receptor po
251 ient receptor potential V1 and M8 (transient receptor potential vanilloid 1 and transient receptor po
256 influx signals through endothelial transient receptor potential vanilloid 4 (TRPV4(EC) ) channels pla
258 evious work suggests activation of transient receptor potential vanilloid 4 (TRPV4) channels by mecha
259 lular Ca(2+) through activation of transient receptor potential vanilloid 4 (TRPV4) channels in the p
260 re we define the overexpression of transient receptor potential vanilloid 4 (TRPV4) in a subgroup of
261 ssembly, and hypothesized that the transient receptor potential vanilloid 4 (TRPV4) ion channel, a me
262 he volume-sensitive machinery, the transient receptor potential vanilloid 4 (TRPV4) ion channel, may
266 t the mechanosensitive ion channel transient receptor potential vanilloid 4 (TRPV4) regulates tumor a
267 we report that genetic ablation of transient receptor potential vanilloid 4 (TRPV4), a Ca(2+)-permeab
269 Our previous study showed that transient receptor potential vanilloid 4 (TRPV4), a mechanosensiti
270 e mechanosensitive cation channel, transient receptor potential vanilloid 4 (TRPV4), alters the in vi
271 sin II receptor type 1 (AT1R), and transient receptor potential vanilloid 4 (TRPV4), in primary murin
272 of a mechanosensitive ion channel, transient receptor potential vanilloid 4 (TRPV4), significantly re
277 er sensing by CD4 T cells involved transient receptor potential vanilloid cation channels (TRPVs) sin
279 ic oxide-sensitive cation channel, transient receptor potential vanilloid family member 1 (TRPV1), an
280 anosensitive cation channel in the transient receptor potential vanilloid family, protects TRPV4 knoc
281 on-selective cation channel TRPV1 (transient receptor potential vanilloid isoform 1) remains elusive.
283 that Piezo1 stimulation triggered transient receptor potential vanilloid subfamily 4 (TRPV4) channel
284 mbrane calcium channels Piezo1 and transient receptor potential vanilloid subfamily 4 (TRPV4) in acin
286 inhibition.SIGNIFICANCE STATEMENT Transient receptor potential vanilloid subtype 1 (TRPV1) has been
290 nociceptive cation channel TRPV1 (transient receptor potential vanilloid type 1) modulates RGC Ca(2+
291 ition, our study revealed that the transient receptor potential vanilloid type 1-dependent increase o
292 In LBCs, we demonstrated that transient receptor potential vanilloid type 2 channel (TRPV2), rep
295 910 (a selective antagonist of the transient receptor potential vanilloid type-1 receptor, TRPV1).
296 both acid-sensing ion channels and transient receptor potential vanilloid type-1 receptors, indicatin
297 dy was to assess whether pulmonary transient receptor potential vanilloid type-4 (TRPV4) mechanorecep
299 , and calcium salts also activated transient receptor potential vanilloid-1 (TRPV1) and transient rec
300 or potential ankyrin-1 (TRPA1) and transient receptor potential vanilloid-3 (TRPV3) agonists can affe