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1 endoplasmic reticulum (ER) Ca(2+) sensor for store-operated channels.
2 eins constitute pore-forming subunits of the store-operated channels.
3 activity without significantly affecting the store-operated channels.
4 association between TRPCs generate distinct store-operated channels.
5 365, suggesting that the influx is via leaky store-operated channels.
6 suggests that they are due to Ca2+ entry via store-operated channels.
7 n-excitable cells Ca2+ influx is mediated by store-operated channels.
8 nce oscillation frequency in addition to the store-operated channels.
9 nnels, mammalian TRP channels, and mammalian store-operated channels.
10 for exploring the physiological functions of store-operated channels.
11 mechanism for distribution and regulation of store-operated channels.
12 ellular Ca2+, rather than directly acting on store-operated channels.
13 ggers Ca(2+) influx through plasma membrane "store-operated" channels.
14 or SKF 96365 (3 x 10(-5) M), an inhibitor of stores-operated channels.
17 STIM1 and STIM2 and their different roles in store-operated channel activation are indicative of an a
19 2+(o)-induced differentiation, but augmented store-operated channel activity and Ca2+ uptake by intra
20 rgin, a known activator of calcium entry via store-operated channels, all increased lung endothelial
21 mammalian Htrp3 protein forms a well defined store-operated channel and so provides a suitable system
22 ound DES to be a very effective inhibitor of store-operated channels and Ca(2+) influx in a variety o
23 tional iPLA(2) is required for activation of store-operated channels and capacitative Ca(2+) influx i
25 ed from Ca(2+)-dependent inactivation of the store-operated channels and does not involve changes in
26 d channels, a gene family that includes Ca2+ store-operated channels and inositol 1,4,5-trisphosphate
28 ticulum, by subsequent calcium entry through store-operated channels, and by increased calcium sensit
29 ther hand, both SKF 96365, a blocker of Ca2+ store-operated channels, and external Na+ removal suppre
30 ut it enters these cells only poorly through store-operated channels, and it is not sequestered by in
31 alcium sensor that initiates the assembly of store-operated channels, and the calcium-independent pho
32 arguing that receptor-stimulated rather than store-operated channels are involved in these sustained
35 eins, do not serve as functional subunits of store-operated channels but do function as subunits for
36 critically dependent on Ca(2+) entry through store-operated channels but do not depend strongly on Ca
38 hibition is not due to calcium entry through store-operated channels but rather results from calcium
39 eviously we have described the properties of store-operated channel currents (SOCs) in freshly disper
40 pear to possess different characteristics to store-operated channels described in other vascular smoo
41 at birth is related to calcium entry through store-operated channels, encoded by the transient recept
44 TIM2 differ in the ability to activate these store-operated channels; Imin channels are regulated by
45 if TrpC1 protein (encoded by trp1 gene) is a store-operated channel in freshly isolated smooth muscle
46 ular Ca(2+) stores and likely to be a native store-operated channel in vascular smooth muscle cells (
47 ltage-gated channels are less important than store-operated channels in the control of airway smooth
48 -based techniques to investigate the role of store-operated channels in the maintenance of hormone-in
49 t TRPC4 channels behave as receptor, but not store-operated, channels in neuronally derived cells.
50 enhancement of SOCE activities sensitive to store-operated channel inhibitors (SKF-96365 and BTP2) a
56 nnel, in regulating Ca(2+) entry through the store-operated channels mouse transient receptor potenti
57 , we show that pharmacological inhibition of store operated channels or reduction in the expression o
60 Orai1 are the long sought components of the store-operated channels required in T-cell activation.
61 Nevertheless, until recently, no candidate store-operated channel (SOC) had been identified molecul
62 phate (PIP(2)) was studied on a native TRPC1 store-operated channel (SOC) in freshly dispersed rabbit
65 nisms, some have been reported to be calcium-store-operated channels (SOC), and others are activated
69 in mediating activation of Ca(2+)-permeable store-operated channels (SOCs) by noradrenaline in rabbi
70 asmic reticulum (SR) Ca(2+) stores activates store-operated channels (SOCs) composed of canonical tra
71 tial), is the founding member of a family of store-operated channels (SOCs) conserved from C. elegans
74 ion channel that mediates Ca2+ entry through store-operated channels (SOCs) in human endothelial cell
75 anism for coupling between Ca(2+) stores and store-operated channels (SOCs) is an important but unres
76 anism for coupling between Ca(2+) stores and store-operated channels (SOCs) is an important but unres
77 m ion (Ca2+) stores and plasma membrane (PM) store-operated channels (SOCs) is crucial to Ca2+ signal
79 or potential channel 1 (TRPC1) protein-based store-operated channels (SOCs) mediates Ca(2+) entry pat
80 or potential channel 1 (TRPC1) protein-based store-operated channels (SOCs) mediates Ca(2+) entry pat
82 (ER) Ca(2+) stores and plasma membrane (PM) store-operated channels (SOCs) remains elusive [1-3].
84 POINTS: Depletion of Ca(2+) stores activates store-operated channels (SOCs), which mediate Ca(2+) ent
92 ] connects the ER Ca(2+)-release channel and store-operated channels; strong evidence for either mech
93 release-activated calcium (CRAC) channel, a store-operated channel that is central to Ca(2+) signali
94 nflux in smooth muscle cells, but the native store-operated channels that mediate such influx remain
96 xtracellular Ca2+ entry via the plasmalemmal store-operated channel transient receptor potential cano
97 a novel role for mitochondria in regulating store-operated channels under physiological conditions.
98 that in the CK1.4 cells, Ca2+ entry through store-operated channels was counteracted by Na+o-depende
99 common view of the TRP family as comprising store-operated channels, we propose that many TRPC heter
100 channel currents with similar properties to store-operated channels were observed in some patches.
101 and TRPC7 participate in forming heteromeric store-operated channels, whereas TRPC3 and TRPC7 can als
102 nt evidence that they belong to the class of store-operated channels, which are activated upon passiv
103 in DT40 cells was similar to the endogenous store-operated channels, with essentially 100% block of
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