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2 at the stimulation-induced redistribution of stromal interaction molecule-1, a critical event for the
3 I(SkCRAC) was reduced by siRNA knockdown of stromal interaction molecule 1 and expression of dominan
4 -activated Ca(2+) (CRAC) channels encoded by stromal interaction molecule 1 and Orai1 are a major rou
7 sion levels of some SOCE components, such as stromal interaction molecule 1, calcium release-activate
8 stores, and a second phase involving STIM 1 (stromal interaction molecule 1) clustering and CRAC (cal
10 or activated protein kinase C-1), and STIM1 (stromal interaction molecule 1) interact with Orai1 upon
13 ric, calcium-selective channels activated by stromal interaction molecule 1 (STIM1) after depletion o
14 3 enhances the signal-induced association of stromal interaction molecule 1 (STIM1) and Orai1 and is
17 xpress the two molecular components of SOCE--stromal interaction molecule 1 (Stim1) and Orai1--and ex
18 ed, whereas the expression of Ca(2+) -sensor stromal interaction molecule 1 (STIM1) and store-operate
19 ditions that induce contacts mediated by the stromal interaction molecule 1 (STIM1) and the Ca(2+) ch
20 the endoplasmic reticulum (ER) Ca(2+) sensor stromal interaction molecule 1 (STIM1) and the Ca(2+) re
21 lcium channel are the Ca(2+)-sensing protein stromal interaction molecule 1 (STIM1) and the channel p
22 ding the Ca2+ channel ORAI1 or its activator stromal interaction molecule 1 (STIM1) are immunodeficie
33 +) entry mechanism in most cancer cells, and stromal interaction molecule 1 (STIM1) is the endoplasmi
35 e, we show that Ca(2+) signaling governed by stromal interaction molecule 1 (STIM1) plays a central r
37 protein ORAI1 or the Ca(2+) sensing protein stromal interaction molecule 1 (STIM1) result in severe
38 the endoplasmic reticulum (ER) Ca(2+) sensor stromal interaction molecule 1 (STIM1) to ER-plasma memb
39 ntration triggers its Ca(2+) ssensor protein stromal interaction molecule 1 (STIM1) to oligomerize an
40 re fully reconstituted via two proteins, the stromal interaction molecule 1 (STIM1), a Ca(2+) sensor
42 amines this issue by focusing on the role of stromal interaction molecule 1 (STIM1), an endo/sarcopla
43 ular myocytes, the physiological function of stromal interaction molecule 1 (STIM1), an endo/sarcopla
44 rexpression of fluorescently tagged RyR2 and stromal interaction molecule 1 (STIM1), an ER Ca(2+) sen
45 n, TRPC1 interaction with the SOCE modulator stromal interaction molecule 1 (STIM1), and Ca(2)(+) ent
46 tion of store operated Ca(2+) entry involves stromal interaction molecule 1 (STIM1), localized to the
47 hannel gating by the CRAC channel activator, stromal interaction molecule 1 (STIM1), remains unknown.
48 vel truncating mutation in the gene encoding stromal interaction molecule 1 (STIM1), the endoplasmic
49 calcium stores results in the aggregation of stromal interaction molecule 1 (STIM1), the endoplasmic
52 ticulum (ER) triggers the oligomerization of stromal interaction molecule 1 (STIM1), the ER Ca(2+) se
53 the redistribution of the ER Ca(2+) sensor, stromal interaction molecule 1 (STIM1), to peripheral si
54 of the transmembrane Ca(2+) sensor protein, stromal interaction molecule 1 (STIM1), to the junctions
56 depletion, which redistributes and clusters stromal interaction molecule 1 (STIM1), which then coclu
57 (CRAC)-mediated capacitive Ca(2+) entry, and stromal interaction molecule 1 (STIM1)- and Orai1-defici
61 ore-operated Ca(2+) entry pathway, involving stromal interaction molecule-1 (STIM1) and Orai1, but al
62 n the molecular machinery that mediate SOCE: stromal interaction molecule-1 (STIM1), which functions
66 rotein levels of Orai1, TRPC1, -C4, -C5, and stromal interaction molecule 1 through MR activation.
67 ce-site mutation in STIM1, the gene encoding stromal interaction molecule 1, which regulates store-op
68 and the endoplasmic reticulum Ca(2+) sensor stromal interaction molecule 1 with CD20 and CD95 into a
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