ライフサイエンスコーパス: calcium depletion

1 of a protein specifically in response to ER calcium depletion.

2 immunoglobulin E (IgE)-binding capacity upon calcium depletion.

3 chaperones, including CRT, is induced by ER calcium depletion.

4 ote phagocytic uptake of cells subject to ER calcium depletion.

5 tight junctions from disassembly induced by calcium depletion.

6 ong dimer that was unable to dissociate upon calcium depletion.

7 ion of AJC by using a model of extracellular calcium depletion.

8 contacts and adhesive dimers in response to calcium depletion.

9 shock and tunicamycin treatments), and upon calcium depletion.

10 nectin-1, over the entire cell surface after calcium depletion.

11 be infected by HSV and PRV, before and after calcium depletion.

12 e infected by HSV-1 and PRV were enhanced by calcium depletion.

13 onsible for only a portion of the effects of calcium depletion.

14 s required for maximal induction by ATF6 and calcium depletion.

15 PD098059 (a MAPK kinase (MEK) inhibitor) and calcium depletion.

16 y which grp78 transcription is stimulated by calcium depletion.

17 Environmental signals such as calcium depletion activate the type III secretion channe

18 pe III secretion system (T3SS) is induced by calcium depletion and is positively regulated by the Exs

19 ock RyR2-Ser2808 phosphorylation-mediated ER calcium depletion and podocyte injury in ER-stressed pod

20 This binding was decreased by calcium depletion and was partially prevented by ligands

21 nslocated to contractile F-actin rings after calcium depletion, and siRNA-mediated depletion of GEF-H

22 Thus, SERCA2 induction in response to calcium depletion appears to be a potentially physiologi

23 ation in Strn-Mlck alters sensitivity to the calcium depletion attributable to chlorantraniliprole's

24 -fold, when cells are subjected to transient calcium depletion before and during infection.

25 Calcium depletion by BAPTA or Ca(2+)-free medium blocked

26 eIF2alpha phosphorylation in response to ER calcium depletion by TZDs.

27 Lumenal ER calcium depletion caused rapid oligomerization of mammal

28 a ER calcium sensor that responds to luminal calcium depletion, changing its oligomeric state and act

29 Calcium depletion decreases GAT1 surface expression by d

30 -induced contractility reduction and partial calcium depletion delay the initial segregation but ceas

31 In marked contrast, calcium depletion did not induce DNA degradation in cont

32 Calcium depletion did not influence BCR-induced Akt phos

33 Calcium depletion dissociates adhesive dimers and promot

34 ing store-operated calcium entry activation, calcium depletion from the endoplasmic reticulum trigger

35 lated during 30 min periods of extracellular calcium depletion in a region enriched with presynaptic

36 GLuc-SERCaMPs revealed ER calcium depletion in rat primary neurons exposed to vari

37 Calcium depletion in root tips with EGTA and A-23187 dec

38 Finally, there is a strong synergy between calcium depletion in the ER and sterile IL-6, as well as

39 ine storage in the acidic compartment led to calcium depletion in these organelles, which then result

40 We further show that Ecadherin mutations and calcium depletion induce structural alterations that pro

41 Calcium depletion induced reorganization of apical F-act

42 for a chaperone and that heat treatment and calcium depletion induced the formation of calnexin dime

43 Our data also indicate that calcium depletion-induced SV40 capsid disassembly may oc

44 determine whether disruption of junctions by calcium depletion influenced the susceptibility of epith

45 trastructural analysis revealed that luminal calcium depletion is accompanied by increased accumulati

46 ar the resting level, whereas a threshold of calcium depletion is required for STIM1 activation [4].

47 calcium refilling mechanism responsive to ER calcium depletion, is enhanced in SOD1G93A astrocytes.

48 ate for the first time that specific luminal calcium depletion leads to a significant decrease in end

49 icing and BiP expression, suggesting that ER calcium depletion may be one factor contributing to ER s

50 Using a calcium depletion model in T84 epithelial cells, we prev

51 In our experimental scenarios, calcium depletion modulates platelet-cancer cell interac

52 TIM2 are calcium-sensing molecules that link calcium depletion of the endoplasmic reticulum with open

53 ncta formation near the plasma membrane upon calcium depletion of the ER.

54 The effect of light and calcium depletion on in vivo protein phosphorylation was

55 Here we show that heat shock, calcium depletion, or deletion of the C-terminal acidic

56 vity was associated with both slower initial calcium depletion rate and increased average calcite cry

57 pletions in sulfur and possible aluminum and calcium depletions, relative to ordinary chondrites, may

58 Calcium depletion resulted in activation of Rho GTPase a

59 ER calcium depletion robustly activates the unfolded protei

60 8 induction by ATF6 in cells subjected to ER calcium depletion stress mediated by thapsigargin (Tg) t

61 When mammalian cells are subjected to calcium depletion stress or protein glycosylation block,

62 tricular myocytes was not increased by SR/ER calcium depletion, suggesting that not all secreted prot

63 We postulated that SR/ER calcium depletion triggered MANF secretion by decreasing

64 nsduction in high-grade DCIS cells, reducing calcium depletion, volume reduction, and motility.

65 olymerized as [Ca(2+)] went down: fully when calcium depletion was maximal (a condition achieved with

66 SERCA2 promoter induction by calcium depletion was partially blocked by dominant-nega

67 A change in conformation of desmoglein 1 by calcium depletion was shown, with immunofluorescence and

68 Using a model of calcium depletion, we defined the pathway of internaliza

69 To explain the mechanism of ER calcium depletion, we hypothesized that FC enrichment of

70 ients, including gap junction inhibition and calcium depletion, were also found to disrupt the develo