戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 terest (VOI; left and right kidneys strongly coclustered).
2 matic redistribution of STIM1 and Orai1 into coclusters.
3 ix domain of Gag are required for Gag-PSGL-1 coclustering.
4 toplasmic domain significantly enhanced this coclustering.
5 or PDGF to evoke complete redistribution and coclustering.
6 played little, if any, pattern of functional coclustering.
7 al experiment modeling and varying levels of coclustering.
8  a single molecule triggered their nanoscale coclustering.
9 ating its synaptic localization and receptor coclustering activity, which could represent molecular s
10 d into 5 disjoint subtypes by a bootstrapped coclustering algorithm with an overall agreement of 98.8
11 internalization by disrupting BCR-lipid raft coclustering and by inducing the endocytosis of raft-bou
12                      uPAR and beta3 integrin coclustering and RET were also observed on tumor cells a
13 l interaction molecule 1 (STIM1), which then coclusters and activates Orai1.
14                        Axonal synapsin-Hsc70 coclusters are also visualized by two-color superresolut
15                                          The coclusters are gently ionized using nanoelectrospray and
16 terminants, in the present study we examined coclustering between Gag and the transmembrane proteins
17  enrichment of an acidic phospholipid drives coclustering between viral structural and cellular trans
18 d that PIP(2) depletion diminishes nanoscale coclustering between viral structural protein Gag and th
19                           M2 and M1 strongly cocluster, but the association of M1 with HA or NA is de
20 ggest that synaptic aggregation and receptor coclustering depend on PICK1 binding to a target membran
21 Coexpression in heterologous systems induces coclustering dependent upon the extreme C terminus of mG
22 vity relationship was determined by assaying cocluster formation with its ligand in heterologous cell
23 ion of GABA(A)R was able to redistribute and cocluster gephyrin by a mechanism requiring a neuron-spe
24 adaptor protein LAT, and tyrosine kinase Lck cocluster in discrete microdomains in the plasma membran
25 tors alpha(5)beta(1) integrin and syndecan-4 cocluster in focal adhesions and coordinate cell migrati
26 ed that these molecules do not significantly cocluster in the cell membrane, arguing against the poss
27                       HA and M2 are strongly coclustered in the plasma membrane; however, in the case
28 nt with previously reported spacings between coclusters in mammalian cells.
29                                  RAS protein coclustering is mainly mediated by membrane association-
30 orms coprecipitate with MMP-9 and CD44/MMP-9 coclustering is observed to be dependent on the ability
31 zation microscopy revealed that Gag-tetherin coclustering is significantly reduced but persists at in
32 blish a quantitative framework to understand coclustering-mediated metabolic channeling and its appli
33 ent a quantitative model to demonstrate that coclustering multiple enzymes into compact agglomerates
34 self-association but that all three diminish coclustering of AChR with rapsyn.
35 in assays of cell surface cluster formation, coclustering of AMPA receptors, and excitatory synaptoge
36 may influence cytoskeleton rearrangement and coclustering of CD3, which likely impact initiation of s
37 dicating continued evolutionary pressure for coclustering of enzymatic genes encoding components of r
38 method for Bayesian model-based hierarchical coclustering of gene expression data and use it to study
39                                  The unusual coclustering of genes associated with different pathways
40 ls in the presence of Homer and mediates the coclustering of Homer with PSD-95/GKAP.
41 selectin to PMNs in suspension also elicited coclustering of L-selectin and PSGL-1 that was signaled
42 , a clinical MEK inhibitor (MEKi), a similar coclustering of NRas and BRAF was observed upon EGF acti
43                                          The coclustering of receptors that regulate angiogenesis may
44 NR1 and NR2B subunits in dendrites, enhanced coclustering of these subunits with the postsynaptic den
45 K1 and mGluR7a in heterologous cells induces coclustering of these two proteins.
46     External cross-linking of Thy-1 promotes coclustering of Thy-1 with LAT, but not with GM1.
47 time series for each experiment and performs coclustering on the genes by optimizing a joint probabil
48 eptor for immunoglobulin (Ig) G (FcgammaRII) coclustering provides a dominant negative signal that bl
49 in synaptic aggregation of PICK1 and mGluR7a coclustering, several PICK1 mutants were generated to an
50 ropod transmembrane proteins PSGL-1 and CD43 cocluster specifically with Gag assembling at the plasma
51 he model predicts the separation and size of coclusters that maximize metabolic efficiency, and this
52 al clustering analysis revealed samples that coclustered tightly with NPC.
53 kably, there is a large increase in receptor coclustering when cells are simultaneously treated with
54 ynergistic activity induced when these cells cocluster with conventional dendritic cells presenting A
55                 We found that Notch and Numb cocluster with the TCR at the APC contact during Ag-driv
56         Second, most Alu elements tend to be coclustered with each other, but recently retroposed ele
57   At the subcellular level, Kv5.1 protein is coclustered with Kv2.1 and Kv2.2 at presumptive ER-PM ju
58                   As the latter group of TFs coclustered with osteogenesis-specific TFs, they may pla
59 on of actin comets was strongly inhibited by coclustering with an inositol 5-phosphatase domain to de
60 ic tails of CD43 and CD44 also promote their coclustering with Gag.
61 uropod-directed protein, showed no or little coclustering with Gag.
62  tail of PSGL-1 significantly enhanced their coclustering with Gag.
63        Lipidation of LC3 is required for its coclustering with Pcdh-gamma tubules, suggesting the inv
64 ew GFP-Bassoon into the axons and subsequent coclustering with SVs.
65 ucing membrane curvature showed little or no coclustering with tetherin in superresolution analyses.
66 ing Gag mutants that are defective in either coclustering with these host proteins or ESCRT-dependent
67 istributes to form a ringlike structure that coclusters with endothelial ICAM-1 as the neutrophil tra
68                          Severe asthma often coclusters with highly allergic children.
69 A is recruited to the cortex by KANK1, which coclusters with liprin-alpha1/beta1 and the components o
70 d demonstrate that Abeta(1-42) peptides form coclusters with membrane mimetic detergent micelles.
71  neurons and to test their ability to induce coclusters with mGluR7a when coexpressed in fibroblast c
72 receptor stimulation, STIM1 translocates and coclusters with Orai1 at sites of close apposition of th
73 oimmunoprecipitates with PSD-95 in vivo, and coclusters with PSD-95 and K+ channels/NMDA receptors in
74             In body-wall muscle cells, CTN-1 coclusters with SLO-1 at regions of dense bodies, which
75 Some proteins, such as HA and M2, inherently cocluster within the membrane, although M2 is found most
76 , very late antigen-4 function, and integrin coclustering within focal adhesive sites on vascular cel
77 strong phylogenetic signal, with individuals coclustering within species, and overall a good agreemen