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2 ric, calcium-selective channels activated by stromal interaction molecule 1 (STIM1) after depletion o
3 3 enhances the signal-induced association of stromal interaction molecule 1 (STIM1) and Orai1 and is
6 xpress the two molecular components of SOCE--stromal interaction molecule 1 (Stim1) and Orai1--and ex
7 ed, whereas the expression of Ca(2+) -sensor stromal interaction molecule 1 (STIM1) and store-operate
8 ditions that induce contacts mediated by the stromal interaction molecule 1 (STIM1) and the Ca(2+) ch
9 the endoplasmic reticulum (ER) Ca(2+) sensor stromal interaction molecule 1 (STIM1) and the Ca(2+) re
10 lcium channel are the Ca(2+)-sensing protein stromal interaction molecule 1 (STIM1) and the channel p
11 ding the Ca2+ channel ORAI1 or its activator stromal interaction molecule 1 (STIM1) are immunodeficie
22 +) entry mechanism in most cancer cells, and stromal interaction molecule 1 (STIM1) is the endoplasmi
24 e, we show that Ca(2+) signaling governed by stromal interaction molecule 1 (STIM1) plays a central r
26 protein ORAI1 or the Ca(2+) sensing protein stromal interaction molecule 1 (STIM1) result in severe
27 the endoplasmic reticulum (ER) Ca(2+) sensor stromal interaction molecule 1 (STIM1) to ER-plasma memb
28 ntration triggers its Ca(2+) ssensor protein stromal interaction molecule 1 (STIM1) to oligomerize an
29 re fully reconstituted via two proteins, the stromal interaction molecule 1 (STIM1), a Ca(2+) sensor
31 amines this issue by focusing on the role of stromal interaction molecule 1 (STIM1), an endo/sarcopla
32 ular myocytes, the physiological function of stromal interaction molecule 1 (STIM1), an endo/sarcopla
33 rexpression of fluorescently tagged RyR2 and stromal interaction molecule 1 (STIM1), an ER Ca(2+) sen
34 n, TRPC1 interaction with the SOCE modulator stromal interaction molecule 1 (STIM1), and Ca(2)(+) ent
35 tion of store operated Ca(2+) entry involves stromal interaction molecule 1 (STIM1), localized to the
36 hannel gating by the CRAC channel activator, stromal interaction molecule 1 (STIM1), remains unknown.
37 vel truncating mutation in the gene encoding stromal interaction molecule 1 (STIM1), the endoplasmic
38 calcium stores results in the aggregation of stromal interaction molecule 1 (STIM1), the endoplasmic
41 ticulum (ER) triggers the oligomerization of stromal interaction molecule 1 (STIM1), the ER Ca(2+) se
42 the redistribution of the ER Ca(2+) sensor, stromal interaction molecule 1 (STIM1), to peripheral si
43 of the transmembrane Ca(2+) sensor protein, stromal interaction molecule 1 (STIM1), to the junctions
45 depletion, which redistributes and clusters stromal interaction molecule 1 (STIM1), which then coclu
46 (CRAC)-mediated capacitive Ca(2+) entry, and stromal interaction molecule 1 (STIM1)- and Orai1-defici
50 I(SkCRAC) was reduced by siRNA knockdown of stromal interaction molecule 1 and expression of dominan
51 -activated Ca(2+) (CRAC) channels encoded by stromal interaction molecule 1 and Orai1 are a major rou
53 rotein levels of Orai1, TRPC1, -C4, -C5, and stromal interaction molecule 1 through MR activation.
54 and the endoplasmic reticulum Ca(2+) sensor stromal interaction molecule 1 with CD20 and CD95 into a
55 stores, and a second phase involving STIM 1 (stromal interaction molecule 1) clustering and CRAC (cal
56 or activated protein kinase C-1), and STIM1 (stromal interaction molecule 1) interact with Orai1 upon
59 sion levels of some SOCE components, such as stromal interaction molecule 1, calcium release-activate
60 ce-site mutation in STIM1, the gene encoding stromal interaction molecule 1, which regulates store-op
63 The endoplasmic reticulum calcium sensors stromal interaction molecules 1 and 2 (STIM1 and STIM2)
66 ore-operated Ca(2+) entry pathway, involving stromal interaction molecule-1 (STIM1) and Orai1, but al
67 n the molecular machinery that mediate SOCE: stromal interaction molecule-1 (STIM1), which functions
68 at the stimulation-induced redistribution of stromal interaction molecule-1, a critical event for the
70 t that mice with T-cell-targeted deletion of Stromal Interaction Molecule (STIM) 1 and STIM2 [double-
74 dered upon binding, the EF-SAM domain in the stromal interaction molecule (STIM) 1 is distinct in tha
78 AC channel function is the identification of stromal interaction molecule (STIM) and ORAI, two essent
80 has revealed that a calcium-binding protein, stromal interaction molecule (STIM), plays an essential
81 of the store-operated Ca(2+) influx mediator stromal interaction molecule (STIM), the plasma membrane
83 eins in the plasma membrane and activated by stromal interaction molecule (STIM)1 and STIM2 in the en
86 ontroversy concerning externalization of the stromal interaction molecule STIM1 upon depletion of Ca(
88 Orai channels and the endoplasmic reticulum stromal interaction molecules (STIMs), is a major Ca(2+)
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