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1 CFP 100+ alpha 25 produced higher levels of blood-feedin
2 CFP and SEM measurements not only allow pore structure a
3 CFP-PAcKer binds more tightly to a full-length variant o
4 CFPs are simple paths in a metabolite-metabolite graph t
5 n, 490 nm detection) was used to image Thy-1 CFP mice aged 6 to 9 months (n = 5) before optic nerve c
7 -6) protein and culture filtrate protein 10 (CFP-10) antigens via the Salmonella type III secretion s
8 aptured antigen is cell filtrate protein 10 (CFP-10) because its Mascot analysis shows a score of 68.
16 t increase in FRET signal between IL-5Ralpha-CFP and betac-YFP was observed in response to IL-5, indi
17 complex recombinant protein antigens ESAT-6, CFP-10, MPB70, and MPB83 elicited delayed-type hypersens
18 e with RASV strains synthesizing SopE-ESAT-6-CFP-10 fusion proteins resulted in significant protectio
19 to M. tuberculosis-specific proteins ESAT-6/CFP-10 by peripheral blood mononuclear cells and CD8(+)
21 response to M. tuberculosis peptides (ESAT-6/CFP-10) between HIV-infected (median CD4+ T-cell count,
22 n of MtbESAT-6, MtbCFP-10, and the MtbESAT-6/CFP-10 heterodimer, by using liposomal model membranes t
24 vel biological role for CFP-10 in the ESAT-6:CFP-10 complex, beyond the previously described chaperon
25 y transfer (FRET)-based probe by inserting a CFP after residue Ser-2367 and a YFP after residue Tyr-2
27 Here we demonstrate that immunization with a CFP-10 DNA vaccine stimulates a specific T-cell response
28 yr-2801 in the cardiac RyR (RyR2) to yield a CFP- and YFP-dual labeled RyR2 (RyR2(Ser-2367-CFP/Tyr-28
31 Median spot-forming units for ESAT-6 and CFP-10 also declined significantly with time (P < 0.001)
32 e application of antigens such as ESAT-6 and CFP-10 for DIVA has so far been realized largely through
33 y, and share sequence features of ESAT-6 and CFP-10 of the Type VII Secretion System (T7SS) of Mycoba
35 growth and in vitro secretion of ESAT-6 and CFP-10, comparing M. tuberculosis to M. africanum and a
38 FP-RIG-I cells, CFP-MDA5:YFP-MDA5 cells, and CFP-MDA5:YFP-LGP2 cells had higher FRET efficiencies in
39 polymer (NIP) was confirmed for CFL, CFD and CFP in standard solutions as well as in milk samples.
44 changes from baseline, determined by FAF and CFP, respectively, were 0.88 (0.1) and 0.78 (0.1) mm(2)
46 The combination of LSSmOrange-mKate2 and CFP-YFP biosensors enabled imaging of apoptotic activity
49 esults reveal good agreement between SEM and CFP measurements for through-pore size distribution.
50 gical activity of CFP-10 has been shown, and CFP-10 has been described as a chaperone protein for ESA
51 associations between climate variability and CFP incidence and suggest that, all other things equal,
55 distinct fluorescent proteins (RFP, YFP and CFP) in neighboring cells, creating a 'Brainbow' of colo
57 rther verifies a positive reaction with anti-CFP-10, indicating that CFP-10 is secreted in the medium
59 n and identify fragments of the MTB antigen, CFP-10, from complex biological samples, without use of
63 ressed neovascularization [NV] at baseline), CFP may be sufficient at baseline and end-of-study visit
64 ddition of IL-5 to cells co-expressing betac-CFP, betac-YFP, and nontagged IL-5Ralpha led to further
68 state), the measured FRET efficiency between CFP (donor in A domain) and FITC (acceptor in N domain)
69 the purified biosensor enhanced FRET between CFP and YFP, consistent with heavy metal-induced folding
71 demic range of CFP, the relationship between CFP incidence and specific environmental conditions is u
72 uorescence resonance energy transfer between CFP-iNOS and beta-arrestin 2-YFP (but not beta-arrestin
73 fluorescent fusion proteins, AT1R-YFP and BK-CFP, displayed robust co-localized Forster resonance ene
75 or in which full-length CaMKII is flanked by CFP and YFP, to measure CaMKII activation state in livin
77 ansfected with wild-type, Y14D, or Y14F Cav1-CFP and -YFP constructs that FRET efficiency was greater
78 alexin (CFX), cefazolin (CFL), cefoperazone (CFP), cloxacillin (CLO), dicloxacillin (DCL), oxacillin
79 Mitochondria in CFP-RIG-I:YFP-RIG-I cells, CFP-MDA5:YFP-MDA5 cells, and CFP-MDA5:YFP-LGP2 cells had
82 molecules (cephalexin (CFL) and cephapirin (CFP)), was prepared by non covalent molecular imprinting
83 R: C3 and C5; complement factor (CF) B, CFD, CFP, CFH and CFI of the AP; and C4 of the classical and
87 ual, N- and C-termini-tagged APP constructs: CFP-APP-YFP [containing the fluorescent tags, cyan fluor
88 erapy by showing that both DNA-HSP65 and CpG/CFP downregulated house dust mite-induced allergic airwa
91 1 allergen were treated with DNA-HSP65, CpG/CFP, or with adoptively transferred cells from immunized
93 ls from mice immunized with DNA-HSP65 or CpG/CFP to allergic recipients downmodulated the allergic re
94 ly, transfer of cells from DNA-HSP65- or CpG/CFP-immunized MyD88(-/-) mice failed to reduce allergy.
96 NKCC1, we tagged the transporter with cyan (CFP) and yellow (YFP) fluorescent proteins at two sites
98 sponse to tumor, suggesting that HSC-derived CFPs serve as an intermediate between the bone marrow an
109 d cyan fluorescent (CFP) tagged ezrin (ezrin-CFP) exist within a complex that has a Forster resonance
111 d as the increase in the donor fluorescence (CFP-NKA-alpha1 or CFP-NKA-alpha2) during progressive acc
112 uggests that GAT1-YFP8 and cyan fluorescent (CFP) tagged ezrin (ezrin-CFP) exist within a complex tha
113 to with the popular term carbon footprints (CFP), are a widely used metric of climate change impacts
116 to monitor the A-N interdomain distance for CFP-SERCA selectively labeled with fluorescein isothiocy
118 The proportion of positive responders for CFP-10 and ESAT-6 between treatment arms was compared us
119 on, representing a novel biological role for CFP-10 in the ESAT-6:CFP-10 complex, beyond the previous
121 her these findings confirm an HSC origin for CFPs, demonstrate a role for MCP1 in regulating their co
122 monstration of a monocyte lineage origin for CFPs, we investigated the role of monocyte chemoattracta
123 ions and the generation of quantitative FRET/CFP ratio images for both sensitized emission and spectr
124 ulatory target, SERCA, we measured FRET from CFP-SERCA or CFP-PLB to YFP-PLB in live AAV-293 cells.
125 uorescently labeled at the N terminus (GAP43-CFP-Galphai/o) seem to faithfully reproduce the behavior
128 rculosis also harbors an encapsulin homolog (CFP-29, Mt-Enc), within an operon with M. tuberculosis D
135 risk of problem shifting when reductions in CFP are obtained at the expense of increase in other env
139 RET pair consists of CFPs and YFPs, but many CFP-YFP reporters suffer from low FRET dynamic range, ph
143 Results showed associations between monthly CFP calls and both warmer SSTs and increased tropical st
144 We estimated associations between monthly CFP incidence in the contiguous United States and SST an
145 strongest association linked current monthly CFP calls to the peak August SST of the previous year.
147 periments conducted using Nox1-YFP and NOXA1-CFP illustrate that NoxA1ds disrupts the binding interac
148 activities, no direct biological activity of CFP-10 has been shown, and CFP-10 has been described as
151 80 with two copies of ESAT-6 and one copy of CFP-10 [SopE(Nt80)-E2C]) afforded protection against aer
153 here was a 16.4% reduction in the density of CFP-positive ganglion cells in the peripheral retina of
154 i mice featuring cell-specific expression of CFP, GFP, YFP or RFP revealed the simultaneous migration
155 cular characteristics and lesion features of CFP/FA and optical coherence tomography (OCT) were evalu
158 scent protein (CFP), emission intensities of CFP and YFP (yellow fluorescent protein) are captured be
159 as of disagreement underscore limitations of CFP-based measurement of drusen, particularly in the siz
164 FRET efficiency was detected in mixtures of CFP- and YFP-tagged full-length Kir6.2 subunits and tran
167 explored the incidence of CFP, percentage of CFP case-patients with laboratory-confirmed ciguatoxic m
168 s Cerulean and Venus, two mutant proteins of CFP and YFP with better folding and less environment sen
169 ate change could expand the endemic range of CFP, the relationship between CFP incidence and specific
171 pair, together with the popular variants of CFP and YFP, for the simultaneous visualization of multi
172 rd genetically encoded FRET pair consists of CFPs and YFPs, but many CFP-YFP reporters suffer from lo
173 roduced MCP1 inhibited in vitro migration of CFPs in response to multiple tumor types, indicating bro
176 e correlated with hyperpigmentary changes on CFP, versus two of 29 (6.9%) control regions (P < 0.001)
178 ironmental management focused exclusively on CFP runs the risk of inadvertently shifting the problem
179 etion of natural resources, and the focus on CFP brings the risk of problem shifting when reductions
181 ecretion via a C-terminal signal sequence on CFP-10 that is recognized by the cytosolic ATPase, Rv387
185 iters to ESAT-6 and production of ESAT-6- or CFP-10-specific gamma interferon (IFN-gamma)-secreting a
186 in the donor fluorescence (CFP-NKA-alpha1 or CFP-NKA-alpha2) during progressive acceptor (PLM-YFP) ph
187 f those had gradable lesion data from FAF or CFP, and 321 had gradable lesion data from both FAF and
191 fter 2-APB addition, binding avidly to Orai1-CFP with a rapid increase in FRET and transiently increa
193 el pathway concept termed carbon flux paths (CFPs) was introduced and benchmarked against existing ap
195 y transfer (FRET) from a circularly permuted CFP mutant to FlAsH, a selectively reactive fluorescein,
200 phy should include color fundus photography (CFP), confocal fundus autofluorescence (FAF), confocal n
201 ectral-domain OCT, color fundus photography (CFP), near-infrared reflectance, and fundus autofluoresc
203 d retinal imaging (color fundus photography [CFP], spectral-domain [SD] optical coherence tomography
205 r the synthesis of two copies of ESAT-6 plus CFP-10 fused to the OmpC signal sequence (OmpC(SS)-E2C)
208 an Union, where the Common Fisheries Policy (CFP) has been criticized for failing to protect stocks [
209 orm of the European Common Fisheries Policy (CFP), which intends to ban discards through the landing
211 The estimated annual incidence of possible CFP was 4.0 per 1,000 person-years, and that of probable
214 r genes, including ProHY5:HY5-GFP and Pro35S:CFP-PIF1, and various FR-HIR-dependent physiological res
222 fluorescent tags, cyan fluorescent protein (CFP) and yellow fluorescent protein (YFP)] and FLAG-APP-
223 tinct spectra: (a) cyan fluorescent protein (CFP) and yellow FP (YFP), and (b) orange FP (mOrange2) a
224 thodology uses the cyan fluorescent protein (CFP) as a biomass indicator and the GFP as a c-di-GMP re
225 e linked to YFP or cyan fluorescent protein (CFP) at N or C termini, and all such constructs, includi
226 localization of a cyan fluorescent protein (CFP) fusion and a protein-protein interaction in Arabido
228 ice that expressed cyan fluorescent protein (CFP) or yellow fluorescent protein (YFP) reporter genes
229 nations to express cyan fluorescent protein (CFP) or YFP fused to either biologically active HCV heli
232 Mice expressing cyan fluorescent protein (CFP) under control of the Thy-1 promoter received MS-275
233 droxylase 1 (Tph1)-cyan fluorescent protein (CFP), c-Kit(wsh/wsh), and Neurog3Cre;ROSA(tdTom) mice by
234 d-to-end fusion of cyan fluorescent protein (CFP), chicken metallothionein II (MT-II), and yellow flu
235 excitation of the cyan fluorescent protein (CFP), emission intensities of CFP and YFP (yellow fluore
236 fer (FRET) between cyan fluorescent protein (CFP)- and yellow fluorescent protein (YFP)-fused RRs in
237 (FRET) analysis of cyan fluorescent protein (CFP)-arm-CTD-yellow fluorescent protein beta-catenin rev
238 ty is localized to cyan fluorescent protein (CFP)-fluorescent RGCs in the B6.Cg-Tg(Thy1-CFP)23Jrs/J m
241 arrying a cyan fluorescent reporter protein (CFP) gene linked to the Thy-1 promoter, which expresses
244 Finally, Rad10-YFP colocalizes with Rad51-CFP and with Rad52-CFP at DSB sites, indicating a tempor
245 FP colocalizes with Rad51-CFP and with Rad52-CFP at DSB sites, indicating a temporal overlap of Rad52
247 odified the experimental system by replacing CFP with the SgrS small RNA, which regulates glucose and
250 t of 20 study eyes, 28 of 39 (71.8%) retinal CFP regions with hyperpigmentation were correlated with
252 ve in interphase; overexpression of stathmin-CFP did not impact metaphase microtubule nucleation rate
256 gher levels of blood-feeding inhibition than CFP alone for susceptible (94 vs 46%, P = 0.001) and res
257 des more biologically relevant pathways than CFP, because canonical pathways are more easily recovere
258 that CFP-10 is a protective antigen and that CFP-10(32-39)-specific CD8+ T cells elicited by vaccinat
260 entury as projected, this model implies that CFP incidence in the United States is likely to increase
261 e reaction with anti-CFP-10, indicating that CFP-10 is secreted in the medium of mycobacterium growth
262 and functional in vitro studies showed that CFPs preferentially migrated and differentiated into fib
266 y investigating the correlations between the CFP and 13 other impact scores, we show that some enviro
267 w FRET dynamic range, phototoxicity from the CFP excitation light and complex photokinetic events suc
276 f the fluorescent retinal neurons in 30 Thy1-CFP mice were obtained using a modified confocal scannin
279 in under control of the Thy-1 promoter (Thy1-CFP mice) to determine how the alpha2-adrenergic agonist
280 in under control of the Thy-1 promoter (Thy1-CFP mice) was imaged using a blue-light confocal scannin
282 = 0.09% versus 0.01%; p = 0.038) but also to CFP-10 (Fo = 0.16% versus 0.007%; p = 0.04) and staphylo
283 on expression of tau or synuclein fusions to CFP and YFP, and confirmed its sensitivity and specifici
284 ere unique among leukocytes in responding to CFP-10, as monocytes and lymphocytes failed to produce a
292 0 mg/m(2)+alpha 25 mg/m(2) was compared with CFP 100 mg/m(2) and alpha 25 mg/m(2) in a small-scale ex
293 measurements using FAF imaging compared with CFP, the measurements were highly correlated with one an
294 vK) of Escherichia coli K12 was flanked with CFP (cyan fluorescent protein) and YFP (yellow fluoresce
296 ransfer (FRET) between receptors tagged with CFP (donor) and receptors tagged with tetracysteine-FlAs
297 FRET between exchanger proteins tagged with CFP or YFP at position 266 within the large cytoplasmic
298 ansfer (FRET) in 293T cells transfected with CFP- and YFP-tagged TNFRs exposed to the thiol oxidant d
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