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1 ation (electron microscopy) and interaction (coimmunoprecipitation).
2 binding sites and can interact with EBNA2 by coimmunoprecipitation.
3 a combination of covalent cross-linking and coimmunoprecipitation.
4 s not interact with Yap1, as demonstrated by coimmunoprecipitation.
5 cence, in situ proximity ligation assay, and coimmunoprecipitation.
6 ween chIL-17RA and chIL-17A was confirmed by coimmunoprecipitation.
7 ed membrane protein 7 (VAMP7) is detected by coimmunoprecipitation.
8 between otoferlin and AP-2 was confirmed by coimmunoprecipitation.
9 Homomultimer formation was confirmed by coimmunoprecipitation.
10 cross-linking, followed by Western blot and coimmunoprecipitation.
11 UALIZED ENDOCYTIC TRAFFICKING DEFECTIVE1) by coimmunoprecipitation.
12 inase B and p38 upstream kinases as shown by coimmunoprecipitation.
13 racts with Rga7 in affinity purification and coimmunoprecipitation.
14 NaC and HDAC7 form a complex, as detected by coimmunoprecipitation.
15 by bioinformatics, immunocytochemistry, and coimmunoprecipitation.
16 tern blotting (WB), immunocytochemistry, and coimmunoprecipitation.
17 he interacting regions have relied mainly on coimmunoprecipitation, a technique with some pitfalls.
18 s stably expressing LANA and was verified by coimmunoprecipitation analyses and with purified protein
20 Forster resonance energy transfer (FRET) and coimmunoprecipitation analyses demonstrated that Gag and
21 vo photocross-linking along with genetic and coimmunoprecipitation analyses dissecting interactions b
22 by >30-fold), subcellular distribution, and coimmunoprecipitation analyses lead us to propose that V
23 escence resonance energy transfer (FRET) and coimmunoprecipitation analyses, we observed increased in
25 nit of integrin alpha2beta1 to platelets and coimmunoprecipitation analysis confirmed integrin alpha2
26 Moreover, an unbiased proteomics screen and coimmunoprecipitation analysis identified Galphas as a n
31 Rab31 was found to interact with the EGFR by coimmunoprecipitation and affinity pulldown analyses, an
32 ntain only the miRNA 3' box was confirmed by coimmunoprecipitation and an in situ proximity ligation
33 d in planta, we further demonstrated by both coimmunoprecipitation and bimolecular fluorescence compl
38 the A2A receptor and SAP102 was verified by coimmunoprecipitation and by tracking its impact on rece
41 and have confirmed this interaction through coimmunoprecipitation and colocalization assays in the C
42 en these two proteins was confirmed by their coimmunoprecipitation and colocalization in cultured cel
43 teraction was confirmed in infected cells by coimmunoprecipitation and colocalization of FAK with P i
44 STAT3 and FLAG-tagged STAT3 and showed using coimmunoprecipitation and colocalization studies that S3
45 B, the p.Gly131Glu mutant VPS33B had reduced coimmunoprecipitation and colocalization with Rab11a and
48 raction of OGT and EZH2/PRC2 was detected by coimmunoprecipitation and cosedimentation experiments.
49 (phox) interacts with cytosolic cortactin by coimmunoprecipitation and double immunofluorescence stai
50 satRNA was confirmed in vivo and in vitro by coimmunoprecipitation and electrophoretic mobility shift
52 hat BAK1 interacts with the BRL1 receptor by coimmunoprecipitation and fluorescence microscopy analys
56 imentin interaction was further confirmed by coimmunoprecipitation and immunofluorescence staining to
58 with NKA-alpha2s in astrocytes, as gauged by coimmunoprecipitation and in situ proximity ligation ass
59 B-Raf(V600E) or K-Ras(G12C/D) Intriguingly, coimmunoprecipitation and in vitro binding assays reveal
61 alidated the mLANA-Hsc70 interaction through coimmunoprecipitation and in vitro glutathione S-transfe
68 20 with dentin sialoprotein was confirmed by coimmunoprecipitation and mass spectrometry analysis of
71 f CESA redundancy in a mutant background, by coimmunoprecipitation and mass spectrometry using label-
75 rgo complexes associated with synapsin using coimmunoprecipitation and multidimensional protein ident
81 ternary complex of BNRF1-Daxx-H3.3-H4, using coimmunoprecipitation and size-exclusion chromatography
82 ring infection as demonstrated by reciprocal coimmunoprecipitation and supported by immunofluorescenc
84 eracted with oligomeric Abeta42, as shown by coimmunoprecipitation and surface plasmon resonance/Biac
85 mouse primary hepatocytes, and mouse livers, coimmunoprecipitation and two-dimensional gel electropho
86 /INPP5F interaction could be demonstrated by coimmunoprecipitation and was potentiated by Rab5, whose
87 Protein-protein interactions were studied by coimmunoprecipitations and a systems biology approach.
88 a putative candidate and through reciprocal coimmunoprecipitations and immunocytochemistry analyses
91 by using flow cytometry, immunofluorescence, coimmunoprecipitation, and gene expression analysis.
92 irmed by glutathione S-transferase pulldown, coimmunoprecipitation, and laser confocal microscopy ass
93 n, bimolecular fluorescence complementation, coimmunoprecipitation, and mass spectrometry analyses su
94 n, bimolecular fluorescence complementation, coimmunoprecipitation, and mass spectrometry analyses su
95 d assays and associates with ABI5 in vivo by coimmunoprecipitation, and the interaction was found in
97 tion, Forster resonance energy transfer, and coimmunoprecipitation approaches revealed that SERK1 int
98 h interactive regions have relied heavily on coimmunoprecipitation approaches, whose limitations incl
101 ed with the EBV immediate early R protein in coimmunoprecipitation assays and partially colocalized w
102 PIs were further supported by the results of coimmunoprecipitation assays and protein structural mode
105 ith fluorescent cellular protein markers and coimmunoprecipitation assays demonstrated that FHV repli
111 more, in silico analysis in combination with coimmunoprecipitation assays show an interaction between
117 bimolecular fluorescence complementation and coimmunoprecipitation assays showed that PYL4-CAR1 as we
118 abidopsis tgd1-1 Coevolutionary analysis and coimmunoprecipitation assays showed that the TGD1 L45 lo
120 EKLF and PIAS proteins confirmed by in vivo coimmunoprecipitation assays with both exogenous and end
122 ction between HSP90 and Tax was validated by coimmunoprecipitation assays, and colocalization between
123 SIVmac239 binding to CD4 in Biacore assays, coimmunoprecipitation assays, and enzyme-linked immunoso
124 3I11) interacted with TRP32 as determined by coimmunoprecipitation assays, colocalization with TRP32
127 n was confirmed by both peptide pulldown and coimmunoprecipitation assays, which also demonstrated th
135 omplementary inactive AR mutants and promote coimmunoprecipitation between unlike forms of AR suggest
137 unctions, we used two complementary methods, coimmunoprecipitation (co-IP) and proximity biotinylatio
138 , we developed in vivo beta-importin complex coimmunoprecipitation (co-IP) assays using budding yeast
140 hromatin immunoprecipitation (ChIP), protein coimmunoprecipitation (Co-IP), and bimolecular fluoresce
142 experimental and computational methods for a coimmunoprecipitation (Co-IP)-based workflow from sample
145 of lepidopteran microtubule transport using coimmunoprecipitation, colocalization, yeast two-hybrid,
156 brain and formed a complex in vivo based on coimmunoprecipitation experiments and coimmunostaining i
161 Immunoprecipitation/mass spectrometry and coimmunoprecipitation experiments confirmed that PLD4 bi
175 r gH/UL116 complex formation was obtained by coimmunoprecipitation experiments on both transfected an
176 , electrophoretic mobility shift assays, and coimmunoprecipitation experiments reveal a specific inte
177 bioinformatics analyses, sequential ChIP and coimmunoprecipitation experiments reveal that Atro inter
180 N-glycosylation inhibitor tunicamycine while coimmunoprecipitation experiments revealed galectin-3 bi
184 imolecular fluorescence complementation, and coimmunoprecipitation experiments show that DRB3 acts do
191 hmwBP complex was corroborated by reciprocal coimmunoprecipitation experiments using antipeptide anti
192 n SH3 binding domain, immunofluorescence and coimmunoprecipitation experiments were conducted and rev
194 7 (aa 693 to 982) was identified by fragment coimmunoprecipitation experiments, and a head-to-tail se
195 romoter reporter and in vitro kinase assays, coimmunoprecipitation experiments, and confocal microsco
196 A time course study of import, followed by coimmunoprecipitation experiments, confirmed that Hsp93
197 RP mutants, FRP:OCP docking simulations, and coimmunoprecipitation experiments, we conclude that the
207 ssociation of these proteins is evident from coimmunoprecipitation followed by mass spectrometry, coe
208 lathrin adaptor proteins AP2-mu2 revealed by coimmunoprecipitation, followed by a decrease in associa
209 east-two hybrid assay, in vitro binding, and coimmunoprecipitation from mouse spermatocytes, we ident
214 for Nm23-H1, verifying their interaction by coimmunoprecipitation in 4T1 cells as well as in human M
215 ed protein 97 (SAP97; also known as DLG1) by coimmunoprecipitation in human embryonic 293 (HEK 293) c
216 -G, both in yeast two-hybrid analysis and by coimmunoprecipitation in situ in HEK293 cells expressing
217 ership of UGT1A_i2 and PKM2 was confirmed by coimmunoprecipitation in the HT115 colon cancer cells an
219 by mass spectrometry analysis as well as RNA coimmunoprecipitation indicated differential binding of
220 ce resonance energy transfer microscopy, and coimmunoprecipitation indicated that LRRC26 was located
225 the two different subunits was confirmed by coimmunoprecipitation of epitope-tagged TREK-1 and TREK-
229 ells and from virion preparations, and RIG-I coimmunoprecipitation of infected cell lysates isolated
233 omic analysis also confirmed the interaction/coimmunoprecipitation of PSMA1-GFP with 13/14 proteasoma
236 t incorporates subcellular fractionation and coimmunoprecipitation of tau from human AD and non-demen
238 e SKAP55 dimerization motif (DM) enabled the coimmunoprecipitation of the Rap1-dependent integrin reg
244 f this phosphorylation site does not prevent coimmunoprecipitation of yAsf1 and Rad53 from yeast extr
248 ery after photobleaching beam-size analysis, coimmunoprecipitation, quantitative imaging, and far-Wes
254 the TRIF B helix residues affected TRIF-TRAM coimmunoprecipitation selectively, as these mutations di
256 esting down-regulation of Wnt signaling, and coimmunoprecipitation showed AQP1 interaction with beta-
259 ative polyacrylamide gel electrophoresis and coimmunoprecipitation showed that STIM1 in the heart exi
263 n of type 1 PI3K with MT was demonstrated by coimmunoprecipitation, showing both PI3K subunits and in
264 was demonstrated in coimmunofluorescence and coimmunoprecipitation studies after overexpression of L2
274 D failed to induce Akt phosphorylation, and coimmunoprecipitation studies indicated that Akt interac
280 play between the activities of EAAT and NCX, coimmunoprecipitation studies showed a physical interact
283 Glutathione S-transferase pull-down and coimmunoprecipitation studies showed the alpha-actinin-4
284 st of these interactions are implicated from coimmunoprecipitation studies using expressed components
285 tion of LD22-4 with U87MG cells, LD22-4-NRP1 coimmunoprecipitation studies, and binding of LD22-4 to
289 ployed live-cell imaging, gene silencing and coimmunoprecipitation to investigate the requirement of
291 naptosome fractionation, immunostaining, and coimmunoprecipitation, we found that Celsr3 and Vangl2,
292 By far-Western blotting, and verified by coimmunoprecipitation, we observed that MBP-1 interacts
296 ding Western blot, immunohistochemistry, and coimmunoprecipitation, were used to determine the expres
298 eletion of the PLCbeta3 PDZ ligand inhibited coimmunoprecipitation with M3R and M3R-dependent PLCbeta
299 found in chorea-acanthocytosis based on Lyn coimmunoprecipitation with Ulk1 and Atg7 and on the pres
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