ライフサイエンスコーパス: cocluster

1 matic redistribution of STIM1 and Orai1 into coclusters.

2 or PDGF to evoke complete redistribution and coclustering.

3 played little, if any, pattern of functional coclustering.

4 al experiment modeling and varying levels of coclustering.

5 ix domain of Gag are required for Gag-PSGL-1 coclustering.

6 toplasmic domain significantly enhanced this coclustering.

7 ating its synaptic localization and receptor coclustering activity, which could represent molecular s

8 internalization by disrupting BCR-lipid raft coclustering and by inducing the endocytosis of raft-bou

9 uPAR and beta3 integrin coclustering and RET were also observed on tumor cells a

10 l interaction molecule 1 (STIM1), which then coclusters and activates Orai1.

11 Axonal synapsin-Hsc70 coclusters are also visualized by two-color superresolut

12 terminants, in the present study we examined coclustering between Gag and the transmembrane proteins

13 M2 and M1 strongly cocluster, but the association of M1 with HA or NA is de

14 ggest that synaptic aggregation and receptor coclustering depend on PICK1 binding to a target membran

15 Coexpression in heterologous systems induces coclustering dependent upon the extreme C terminus of mG

16 vity relationship was determined by assaying cocluster formation with its ligand in heterologous cell

17 ion of GABA(A)R was able to redistribute and cocluster gephyrin by a mechanism requiring a neuron-spe

18 adaptor protein LAT, and tyrosine kinase Lck cocluster in discrete microdomains in the plasma membran

19 tors alpha(5)beta(1) integrin and syndecan-4 cocluster in focal adhesions and coordinate cell migrati

20 ed that these molecules do not significantly cocluster in the cell membrane, arguing against the poss

21 HA and M2 are strongly coclustered in the plasma membrane; however, in the case

22 nt with previously reported spacings between coclusters in mammalian cells.

23 orms coprecipitate with MMP-9 and CD44/MMP-9 coclustering is observed to be dependent on the ability

24 zation microscopy revealed that Gag-tetherin coclustering is significantly reduced but persists at in

25 blish a quantitative framework to understand coclustering-mediated metabolic channeling and its appli

26 ent a quantitative model to demonstrate that coclustering multiple enzymes into compact agglomerates

27 self-association but that all three diminish coclustering of AChR with rapsyn.

28 in assays of cell surface cluster formation, coclustering of AMPA receptors, and excitatory synaptoge

29 dicating continued evolutionary pressure for coclustering of enzymatic genes encoding components of r

30 method for Bayesian model-based hierarchical coclustering of gene expression data and use it to study

31 The unusual coclustering of genes associated with different pathways

32 ls in the presence of Homer and mediates the coclustering of Homer with PSD-95/GKAP.

33 selectin to PMNs in suspension also elicited coclustering of L-selectin and PSGL-1 that was signaled

34 The coclustering of receptors that regulate angiogenesis may

35 NR1 and NR2B subunits in dendrites, enhanced coclustering of these subunits with the postsynaptic den

36 K1 and mGluR7a in heterologous cells induces coclustering of these two proteins.

37 External cross-linking of Thy-1 promotes coclustering of Thy-1 with LAT, but not with GM1.

38 time series for each experiment and performs coclustering on the genes by optimizing a joint probabil

39 eptor for immunoglobulin (Ig) G (FcgammaRII) coclustering provides a dominant negative signal that bl

40 in synaptic aggregation of PICK1 and mGluR7a coclustering, several PICK1 mutants were generated to an

41 he model predicts the separation and size of coclusters that maximize metabolic efficiency, and this

42 al clustering analysis revealed samples that coclustered tightly with NPC.

43 kably, there is a large increase in receptor coclustering when cells are simultaneously treated with

44 ynergistic activity induced when these cells cocluster with conventional dendritic cells presenting A

45 We found that Notch and Numb cocluster with the TCR at the APC contact during Ag-driv

46 Second, most Alu elements tend to be coclustered with each other, but recently retroposed ele

47 As the latter group of TFs coclustered with osteogenesis-specific TFs, they may pla

48 on of actin comets was strongly inhibited by coclustering with an inositol 5-phosphatase domain to de

49 uropod-directed protein, showed no or little coclustering with Gag.

50 tail of PSGL-1 significantly enhanced their coclustering with Gag.

51 ic tails of CD43 and CD44 also promote their coclustering with Gag.

52 Lipidation of LC3 is required for its coclustering with Pcdh-gamma tubules, suggesting the inv

53 ew GFP-Bassoon into the axons and subsequent coclustering with SVs.

54 ucing membrane curvature showed little or no coclustering with tetherin in superresolution analyses.

55 istributes to form a ringlike structure that coclusters with endothelial ICAM-1 as the neutrophil tra

56 Severe asthma often coclusters with highly allergic children.

57 A is recruited to the cortex by KANK1, which coclusters with liprin-alpha1/beta1 and the components o

58 neurons and to test their ability to induce coclusters with mGluR7a when coexpressed in fibroblast c

59 receptor stimulation, STIM1 translocates and coclusters with Orai1 at sites of close apposition of th

60 oimmunoprecipitates with PSD-95 in vivo, and coclusters with PSD-95 and K+ channels/NMDA receptors in

61 In body-wall muscle cells, CTN-1 coclusters with SLO-1 at regions of dense bodies, which

62 Some proteins, such as HA and M2, inherently cocluster within the membrane, although M2 is found most

63 , very late antigen-4 function, and integrin coclustering within focal adhesive sites on vascular cel

64 strong phylogenetic signal, with individuals coclustering within species, and overall a good agreemen