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2 ric, calcium-selective channels activated by stromal interaction molecule 1 (STIM1) after depletion o
3 Upon ER Ca2+ depletion, TRIC-A clusters with stromal interaction molecule 1 (STIM1) and Ca2+-release-
4 ER, a greater degree of interaction between stromal interaction molecule 1 (STIM1) and L-type Ca(2+)
6 3 enhances the signal-induced association of stromal interaction molecule 1 (STIM1) and Orai1 and is
9 xpress the two molecular components of SOCE--stromal interaction molecule 1 (Stim1) and Orai1--and ex
10 ulum (ER)-associated Ca(2+)-sensing proteins stromal interaction molecule 1 (STIM1) and STIM2, which
11 ed, whereas the expression of Ca(2+) -sensor stromal interaction molecule 1 (STIM1) and store-operate
12 ditions that induce contacts mediated by the stromal interaction molecule 1 (STIM1) and the Ca(2+) ch
13 the endoplasmic reticulum (ER) Ca(2+) sensor stromal interaction molecule 1 (STIM1) and the Ca(2+) re
14 lcium channel are the Ca(2+)-sensing protein stromal interaction molecule 1 (STIM1) and the channel p
15 the endoplasmic reticulum (ER) Ca(2+) sensor stromal interaction molecule 1 (STIM1) and the plasma me
16 ding the Ca2+ channel ORAI1 or its activator stromal interaction molecule 1 (STIM1) are immunodeficie
18 e found that deficiency in the Ca(2+) sensor stromal interaction molecule 1 (STIM1) caused spontaneou
20 ls, we bred the 2 Amelx-iCre mice lines with stromal interaction molecule 1 (Stim1) floxed mice to ge
27 rai1 channels, the latter being activated by stromal interaction molecule 1 (STIM1) in response to ER
28 with the endoplasmic reticulum Ca(2+) sensor stromal interaction molecule 1 (STIM1) in response to st
41 asmic reticulum (ER) calcium-sensing protein stromal interaction molecule 1 (STIM1) is critically inv
42 NCE STATEMENT In Purkinje neurons (PNs), the stromal interaction molecule 1 (STIM1) is required for m
43 +) entry mechanism in most cancer cells, and stromal interaction molecule 1 (STIM1) is the endoplasmi
46 ium store depletion, the ER-resident protein stromal interaction molecule 1 (STIM1) physically intera
47 e, we show that Ca(2+) signaling governed by stromal interaction molecule 1 (STIM1) plays a central r
49 protein ORAI1 or the Ca(2+) sensing protein stromal interaction molecule 1 (STIM1) result in severe
50 ut strict Ca(2+) selectivity or based on the stromal interaction molecule 1 (STIM1) that might crosst
51 the endoplasmic reticulum (ER) Ca(2+) sensor stromal interaction molecule 1 (STIM1) to ER-plasma memb
52 e photoreceptors into modular domains of the stromal interaction molecule 1 (STIM1) to manipulate pro
53 ntration triggers its Ca(2+) ssensor protein stromal interaction molecule 1 (STIM1) to oligomerize an
55 endoplasmic reticulum-resident Ca(2+) sensor stromal interaction molecule 1 (STIM1) with the PMCA4b s
56 re fully reconstituted via two proteins, the stromal interaction molecule 1 (STIM1), a Ca(2+) sensor
57 7)-mediated complex between calreticulin and stromal interaction molecule 1 (STIM1), a protein of the
59 amines this issue by focusing on the role of stromal interaction molecule 1 (STIM1), an endo/sarcopla
60 ular myocytes, the physiological function of stromal interaction molecule 1 (STIM1), an endo/sarcopla
61 rexpression of fluorescently tagged RyR2 and stromal interaction molecule 1 (STIM1), an ER Ca(2+) sen
63 n, TRPC1 interaction with the SOCE modulator stromal interaction molecule 1 (STIM1), and Ca(2)(+) ent
65 tion of store operated Ca(2+) entry involves stromal interaction molecule 1 (STIM1), localized to the
67 hannel gating by the CRAC channel activator, stromal interaction molecule 1 (STIM1), remains unknown.
68 found that PMP22 co-immunoprecipitated with stromal interaction molecule 1 (STIM1), the Ca(2+) senso
69 vel truncating mutation in the gene encoding stromal interaction molecule 1 (STIM1), the endoplasmic
70 calcium stores results in the aggregation of stromal interaction molecule 1 (STIM1), the endoplasmic
73 ticulum (ER) triggers the oligomerization of stromal interaction molecule 1 (STIM1), the ER Ca(2+) se
74 the redistribution of the ER Ca(2+) sensor, stromal interaction molecule 1 (STIM1), to peripheral si
75 of the transmembrane Ca(2+) sensor protein, stromal interaction molecule 1 (STIM1), to the junctions
77 asmic reticulum (ER) calcium-sensing protein stromal interaction molecule 1 (STIM1), which interacts
78 depletion, which redistributes and clusters stromal interaction molecule 1 (STIM1), which then coclu
79 (CRAC)-mediated capacitive Ca(2+) entry, and stromal interaction molecule 1 (STIM1)- and Orai1-defici
84 of secretory pathway Ca(2+)-ATPase (SPCA2), stromal interaction molecule 1 (STIM1)/calcium release-a
85 rated Ca(2+) entry (SOCE) channels formed by stromal interaction molecule 1 (STIM1)/Orai complexes, a
87 we examined the role of two Ca(2+) sensors, stromal interaction molecule 1 and 2 (STIM1 and STIM2),
88 y (SOCE) accompanied by the up-regulation of stromal interaction molecule 1 and calcium release-activ
89 I(SkCRAC) was reduced by siRNA knockdown of stromal interaction molecule 1 and expression of dominan
90 -activated Ca(2+) (CRAC) channels encoded by stromal interaction molecule 1 and Orai1 are a major rou
92 ression of the Ca(2+) sensor protein STIM1L (stromal interaction molecule 1 long isoform) in CTEPH my
93 rotein levels of Orai1, TRPC1, -C4, -C5, and stromal interaction molecule 1 through MR activation.
94 and the endoplasmic reticulum Ca(2+) sensor stromal interaction molecule 1 with CD20 and CD95 into a
95 rophil Cracr2a rapidly interacts with Stim1 (stromal interaction molecule 1) after agonist stimulatio
96 stores, and a second phase involving STIM 1 (stromal interaction molecule 1) clustering and CRAC (cal
97 or activated protein kinase C-1), and STIM1 (stromal interaction molecule 1) interact with Orai1 upon
100 ctly with the coiled-coil 2 domain of Stim1 (stromal interaction molecule 1) via its joining region.
103 sion levels of some SOCE components, such as stromal interaction molecule 1, calcium release-activate
104 ce-site mutation in STIM1, the gene encoding stromal interaction molecule 1, which regulates store-op
108 The endoplasmic reticulum calcium sensors stromal interaction molecules 1 and 2 (STIM1 and STIM2)
111 ore-operated Ca(2+) entry pathway, involving stromal interaction molecule-1 (STIM1) and Orai1, but al
112 n the molecular machinery that mediate SOCE: stromal interaction molecule-1 (STIM1), which functions
113 at the stimulation-induced redistribution of stromal interaction molecule-1, a critical event for the
115 t that mice with T-cell-targeted deletion of Stromal Interaction Molecule (STIM) 1 and STIM2 [double-
119 dered upon binding, the EF-SAM domain in the stromal interaction molecule (STIM) 1 is distinct in tha
124 AC channel function is the identification of stromal interaction molecule (STIM) and ORAI, two essent
126 + entry signals triggered by the Ca2+ sensor Stromal Interaction Molecule (STIM) proteins of the endo
128 has revealed that a calcium-binding protein, stromal interaction molecule (STIM), plays an essential
129 of the store-operated Ca(2+) influx mediator stromal interaction molecule (STIM), the plasma membrane
130 ling mechanism in myogenesis, is mediated by stromal interaction molecule (STIM), which senses the de
132 eins in the plasma membrane and activated by stromal interaction molecule (STIM)1 and STIM2 in the en
134 genetic approaches, we demonstrate that the stromal interaction molecule (STIM)2, a calcium sensor,
136 in the plasma membrane and are activated by stromal interaction molecules (STIM) located in the endo
137 ontroversy concerning externalization of the stromal interaction molecule STIM1 upon depletion of Ca(
139 the endoplasmic reticulum (ER) Ca2+ sensors, stromal interaction molecules STIM1 and STIM2, are key r
142 identify endoplasmic reticulum (ER)-resident stromal interaction molecules (STIM1/2), which are Ca(2+
144 Orai channels and the endoplasmic reticulum stromal interaction molecules (STIMs), is a major Ca(2+)