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1 escent protein with the chloride-insensitive cyan fluorescent protein.
2 tro assays and cells overexpressing stathmin-cyan fluorescent protein.
3 ergy transfer (FRET) acceptor for the newest cyan fluorescent proteins.
4 tein kinase A (PKA) consisting of fusions of cyan fluorescent protein, a phosphoamino acid binding do
5 nced yellow fluorescent protein and enhanced cyan fluorescent protein, allowing detection of zinc-ind
6 ore, the septin Cdc12p, fused with yellow or cyan fluorescent protein, also colocalized with Myo1p an
8 otransfected with a mitochondrially targeted cyan fluorescent protein and an enhanced yellow fluoresc
10 red the interaction between DDR1 tagged with cyan fluorescent protein and DDR1 tagged with yellow flu
12 ged the TAP1 and TAP2 subunits with enhanced cyan fluorescent protein and enhanced yellow fluorescent
14 our method, we targeted QDs to cell surface cyan fluorescent protein and epidermal growth factor rec
15 human embryonic kidney 293T cells using H1R-cyan fluorescent protein and H2R-yellow fluorescent prot
17 omain of InsP3 receptors (types 1-3) between cyan fluorescent protein and yellow fluorescent protein
18 ing VP22 and VP13/14 as fusion proteins with cyan fluorescent protein and yellow fluorescent protein,
19 ding the human CrkII1-236 sandwiched between cyan fluorescent protein and yellow fluorescent protein,
20 tes inserted into a linker region separating cyan fluorescent protein and yellow fluorescent protein.
21 ubunits were genetically fused with enhanced cyan fluorescent protein and/or enhanced yellow fluoresc
22 f Escherichia coli K12 was flanked with CFP (cyan fluorescent protein) and YFP (yellow fluorescent pr
23 uorescence resonance energy transfer between cyan fluorescent protein- and yellow fluorescent protein
24 nce resonance energy transfer (FRET) between cyan fluorescent protein- and yellow fluorescent protein
25 icistronic mRNAs encoding enhanced green and cyan fluorescent proteins as the first and second cistro
26 s luciferase, yellow fluorescent protein, or cyan fluorescent protein at the carboxyl terminus of VPA
27 on of calmodulin within Citrine or fusion of cyan fluorescent protein, calmodulin, a calmodulin-bindi
28 e resonance energy transfer between enhanced cyan fluorescent protein-CaM and Na(V)1.5(4X) channels t
29 mouse liver sections after co-expression of cyan fluorescent protein-CCRP and yellow fluorescent pro
30 ts of yellow fluorescent protein (Venus) and cyan fluorescent protein (Cerulean) flank either the ent
31 reticulum Ca2+-ATPase (SERCA) were fused to cyan fluorescent protein (CFP) and coexpressed with PLB
32 maging to detect the proximity between CXCR1-cyan fluorescent protein (CFP) and fluorescence probes t
33 n a pixel-by-pixel basis using EGFR fused to cyan fluorescent protein (CFP) and Grb2 fused to yellow
36 r resonance energy transfer (FRET) pair, the cyan fluorescent protein (CFP) and yellow fluorescent pr
37 FP-APP-YFP [containing the fluorescent tags, cyan fluorescent protein (CFP) and yellow fluorescent pr
38 sfer (FRET) pairs with distinct spectra: (a) cyan fluorescent protein (CFP) and yellow FP (YFP), and
39 nsfer (FRET) of beta1a subunits labeled with cyan fluorescent protein (CFP) and/or yellow fluorescent
42 odel cell system and the standard FRET pair, cyan fluorescent protein (CFP) as the donor and yellow f
43 length Kir6.2 subunits were linked to YFP or cyan fluorescent protein (CFP) at N or C termini, and al
44 nalysis of the subcellular localization of a cyan fluorescent protein (CFP) fusion and a protein-prot
45 ellow fluorescent protein (YFP) and enhanced cyan fluorescent protein (CFP) genes in which recombinat
48 epithelial (LLCPK) cells expressing stathmin-cyan fluorescent protein (CFP) or injected with stathmin
49 of Grb2, Shc, H-Ras, and K-Ras with enhanced cyan fluorescent protein (CFP) or yellow fluorescent pro
50 -length and truncated forms of VacA fused to cyan fluorescent protein (CFP) or yellow fluorescent pro
52 ignalling (RGS4) proteins were each fused to cyan fluorescent protein (CFP) or yellow fluorescent pro
53 by two nonfluorescent fragments (N and C) of cyan fluorescent protein (CFP) or yellow fluorescent pro
54 with various vector combinations to express cyan fluorescent protein (CFP) or YFP fused to either bi
56 otein of 25 kDa (SNAP-25), were used to link cyan fluorescent protein (CFP) to yellow fluorescent pro
57 nal ribosome entry sequence (IRES)-dependent cyan fluorescent protein (CFP) translation were monitore
59 strain was used, containing a construct with cyan fluorescent protein (CFP) under Thy-1 promoter cont
60 otein (YFP) was fused to the N terminus, and cyan fluorescent protein (CFP) was fused to the C termin
61 xtended with a transmembrane (TM) domain and cyan fluorescent protein (CFP) were immobilized in the p
63 variants of green fluorescent protein (GFP), cyan fluorescent protein (CFP), and yellow fluorescent p
64 ROSA(tdTom), tryptophan hydroxylase 1 (Tph1)-cyan fluorescent protein (CFP), c-Kit(wsh/wsh), and Neur
65 ensor is composed of an end-to-end fusion of cyan fluorescent protein (CFP), chicken metallothionein
66 lly confirmed by measurements on mixtures of cyan fluorescent protein (CFP), citrine ((Cit) a yellow
67 icroscopic measurements of fluorescence from cyan fluorescent protein (CFP), citrine, and linked CFP-
69 ter resonance energy transfer (FRET) between cyan fluorescent protein (CFP)- and yellow fluorescent p
70 nance energy transmission (FRET) analysis of cyan fluorescent protein (CFP)-arm-CTD-yellow fluorescen
71 raction between MacMARCKS and dynamitin with cyan fluorescent protein (CFP)-conjugated dynamitin as t
75 Finally, the level and rate of recovery of cyan fluorescent protein (CFP)-M1-5 were lower than thos
78 performed following transient expression of cyan fluorescent protein (CFP)-tagged proteins and incub
82 thesis, cDNA constructs were created to fuse cyan-fluorescent protein (CFP) to the N terminus of SERC
83 uced intracellular redistribution of an EGFR-cyan fluorescent protein chimera was markedly reduced by
86 (FRET) between fusion proteins labeled with cyan fluorescent protein (donor) and yellow fluorescent
87 c for XOPS-mCFP, a membrane-targeted form of cyan fluorescent protein driven by the Xenopus rhodopsin
88 in cells expressing the fusion protein CFP (cyan fluorescent protein)-dynamitin or CFP-MB (the MacMA
89 c mice expressing a synaptotagmin 1-enhanced cyan fluorescent protein (ECFP) fusion protein under con
90 llow fluorescent protein (EYFP) and enhanced cyan fluorescent protein (ECFP) variants of green fluore
91 id carrying the gene coding for the enhanced cyan fluorescent protein (ECFP) was also introduced into
92 protein (EYFP), Ht31 was linked to enhanced cyan fluorescent protein (ECFP), and these constructs we
93 rescent protein (GFP), a variant of enhanced cyan fluorescent protein (ECFP), has been determined to
94 yellow fluorescent protein (EYFP) > enhanced cyan fluorescent protein (ECFP), while a GST construct t
95 anced green fluorescent protein- or enhanced cyan fluorescent protein (ECFP)-tagged phospholipase Cde
101 that contained enhanced yellow and enhanced cyan fluorescent protein (EYFP and ECFP, respectively) l
102 and double label (yellow fluorescent protein/cyan fluorescent protein) fluorescence labeling experime
103 e dynamic range and a 10% increase in donor (cyan fluorescent protein) fluorescence upon bleach of ye
104 assays in plants that constitutively express cyan fluorescent protein fused to histone 2B provides en
105 uorescence resonance energy transfer between cyan fluorescent protein-fused and yellow fluorescent pr
106 an be rescued by overexpression of the PEX12-cyan fluorescent protein fusion protein, which targets t
107 oxisomes, as demonstrated for endogenous and cyan fluorescent protein fusion proteins by fluorescence
109 tween Gialpha-yellow fluorescent protein and cyan fluorescent protein-Gbeta chimeras in HeLa cells.
110 al microscopy of coexpressed YFP-hGRbeta and cyan fluorescent protein-hGRalpha in COS-1 cells indicat
111 ed from phagocytic cups earlier than did p85-cyan fluorescent protein, indicating that SHIP-1 inhibit
112 almodulin, and the FRET donor ECFP (enhanced cyan fluorescent protein) into eNOS at a site adjacent t
113 The advantage over previous constructs using cyan fluorescent protein is that our construct can be us
114 ne the stability of complexes formed between cyan fluorescent protein-labeled alpha(2A)-adrenorecepto
115 fluorescent protein (YFP) move along tubulin-cyan fluorescent protein-labeled microtubules in respons
117 nally, chimeric proteins containing enhanced cyan fluorescent protein linked to wild-type CREB or CRE
121 low fluorescent protein (EYFP)- and enhanced cyan fluorescent protein-NHPX fusions, we show here that
123 s were addressed by tagging tapasin with the cyan fluorescent protein or yellow fluorescent protein (
124 ent colocalization of Akt2 fused with either cyan fluorescent protein or yellow fluorescent protein t
125 E12, E47, E12(NLS), or MyoD(NLS) and either cyan fluorescent protein or yellow fluorescent protein,
126 a fluorescently tagged P-glycoprotein (MDR1-cyan fluorescent protein) permitted the drug-resistant p
128 gion was used to introduce green, yellow and cyan fluorescent protein reporters into B. burgdorferi.
129 ciation with SERCA, measured by FRET between cyan fluorescent protein-SERCA and yellow fluorescent pr
131 sonance energy transfer was detected between cyan fluorescent protein-tagged DAT and yellow fluoresce
133 Co-expression of hemagglutinin-tagged and cyan fluorescent protein-tagged UGT1A proteins, followed
136 een genetically attached enhanced yellow and cyan fluorescent protein to the N or C terminus of the c
137 nsgenic mice in which red, green, yellow, or cyan fluorescent proteins (together termed XFPs) were se
138 gitudinal retinal imaging of mice expressing cyan fluorescent protein under control of the Thy-1 prom
140 cts were used to express SNAP-25 tagged with cyan fluorescent protein, VAMP-2 tagged with yellow fluo
141 t the Trp66 position in the chromophore of a cyan fluorescent protein variant (CFP6) to investigate t
143 used to either yellow fluorescent protein or cyan fluorescent protein we can observe tau fusion prote
144 cell lines stably coexpressing PML-enhanced cyan fluorescent protein with other individual marker pr
145 protein-Dictyostelium myosin II motor domain-cyan fluorescent protein (YFP-myosin-CFP) and compared t
146 his upregulation, we incorporated yellow and cyan fluorescent proteins (YFPs and CFPs) into the alpha
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