ライフサイエンスコーパス: CFP

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

6 L-2 ELISPOT using immunodominant Ags (Acr-1, CFP-10, ESAT-6) as references.

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.

9 -6) protein and culture filtrate protein 10 (CFP-10).

10 sis-specific Ag culture filtrate protein-10 (CFP-10).

11 We obtained information on 1,102 CFP-related calls to U.S. poison control centers during

12 nstructs, including double-tagged YFP-Kir6.2-CFP (Y6.2C), formed functional K(ATP) channels.

13 changes in the clamp region of RyR2(Ser-2367-CFP/Tyr-2801-YFP) induced by various ligands.

14 FP- and YFP-dual labeled RyR2 (RyR2(Ser-2367-CFP/Tyr-2801-YFP)).

15 nds in HEK293 cells expressing RyR2(Ser-2367-CFP/Tyr-2801-YFP).

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(+)

20 The most abundant factor, the ESAT-6/CFP-10 dimer, is targeted for secretion via a C-terminal

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

23 We here show that the ESAT-6:CFP-10 complex induces a transient release of Ca(2+) fro

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

26 Expression of a CFP-CCTalpha mutant lacking residues 290-299 in cells re

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

29 support public health decision making about CFP prevention.

30 In addition, CFPs guarantee carbon exchange in each of their intermed

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

34 ESAT-6 and CFP-10 secretion were similar for all strains, although

35 growth and in vitro secretion of ESAT-6 and CFP-10, comparing M. tuberculosis to M. africanum and a

36 Unlike ESAT-6 and CFP-10, EsxA and EsxB do not interact.

37 sed yellow fluorescent protein (YFP)-CAR and CFP-R16A fusion proteins.

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.

40 ysis led to decarboxylation of CFD, CFX, and CFP.

41 ChAT and CFP expression was evaluated in flat-mounted retinas exa

42 Swapping the C-termini of EspC and CFP-10 revealed that these signals are functionally dist

43 rophic lesion areas were measured by FAF and CFP to assess lesion progression over time.

44 changes from baseline, determined by FAF and CFP, respectively, were 0.88 (0.1) and 0.78 (0.1) mm(2)

45 1 had gradable lesion data from both FAF and CFP.

46 The combination of LSSmOrange-mKate2 and CFP-YFP biosensors enabled imaging of apoptotic activity

47 Both eyes were imaged with SD-OCT and CFP.

48 was measured using YFP-tagged Galpha(q) and CFP-tagged Ggamma(2).

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,

52 We tested wild type (WT) and CFP-NKA-alpha1 point mutants (alanine substitution at F9

53 escence, whereas slightly augmenting YFP and CFP brightness.

54 These aptamers bind GFP, YFP and CFP with low nanomolar affinity and binding decreases GF

55 distinct fluorescent proteins (RFP, YFP and CFP) in neighboring cells, creating a 'Brainbow' of colo

56 Automated image analysis produced another CFP map.

57 rther verifies a positive reaction with anti-CFP-10, indicating that CFP-10 is secreted in the medium

58 and an isolation rate of 90% for the antigen CFP-10.

59 n and identify fragments of the MTB antigen, CFP-10, from complex biological samples, without use of

60 Masked readers assessed CFP and FA.

61 The influenza-associated CFP was 1.8% (57 of 3091), compared with 2.9% (1016 of 3

62 This approach is termed atomic CFP (aCFP).

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

65 Substantial FRET signals with betac-CFP and betac-YFP co-expressed in the absence of IL-5Ral

66 There was general agreement between CFP and SD-OCT in identifying presence and absence of dr

67 was demonstrated in drusen detection between CFP and SD-OCT.

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

70 Donor-dequenching FRET between CFP-tagged KCNQ1-5 and YFP-tagged AKAP79 revealed associ

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

74 oward greater detection of smaller drusen by CFP.

75 or in which full-length CaMKII is flanked by CFP and YFP, to measure CaMKII activation state in livin

76 The best-performing design, called CFP-PAcKer, was based on the third strategy and bound th

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

80 Both central (CFP) and lateral (LFP) variations of the model have been

81 Cefazolin (CFZ) and cephapirin (CFP) underwent mainly direct photolysis (t(1/2) = 0.7, 3

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

84 Mixtures of chlorfenapyr (CFP) and alphacypermethrin (alpha) may provide additiona

85 We have used the Chx10::CFP mouse line to further investigate the properties and

86 ed on drusen presence produced the composite CFP drusen map.

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

89 gulating the Th2 response, DNA-HSP65 and CpG/CFP promoted IL-10 and IFN-gamma production.

90 ctive reduction of allergy by cells from CpG/CFP-immunized mice, Fas molecules were required.

91 1 allergen were treated with DNA-HSP65, CpG/CFP, or with adoptively transferred cells from immunized

92 Although DNA-HSP65 or CpG/CFP immunization stimulated antigen-specific production

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.

95 NA-HSP65 was associated with IL-10 while CpG/CFP was associated with IFN-gamma.

96 NKCC1, we tagged the transporter with cyan (CFP) and yellow (YFP) fluorescent proteins at two sites

97 We defined CFP case-patients as persons with gastrointestinal sympt

98 sponse to tumor, suggesting that HSC-derived CFPs serve as an intermediate between the bone marrow an

99 r AMD were prospectively imaged with digital CFP and SD-OCT.

100 We produced dual CFP/YFP-tagged GluA2 subunit constructs that had normal

101 We inserted either CFP or YFP into the second intracellular loop of mGluR1b

102 Here we demonstrate that C. elegans CFP-1 targets promoters with high CpG density, and these

103 . tuberculosis infection of C3H mice elicits CFP-10-specific CD8+ and CD4+ T cells.

104 We have paired enhanced CFP (ECFP) with YPet, a variant of YFP.

105 ponse only to the H-2K(k)-restricted epitope CFP-10(32-39).

106 EsxA (ESAT-6) and EsxB (CFP-10) are virulence factors exported by the ESX-1 syst

107 inked to the Thy-1 promoter, which expresses CFP in RGCs.

108 In vivo, CCR2-expressing CFPs increased in circulation during the period of activ

109 d cyan fluorescent (CFP) tagged ezrin (ezrin-CFP) exist within a complex that has a Forster resonance

110 dministration of metronidazole to Tg(fabp10a:CFP-NTR) animals.

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

114 sis, compared with 50% for alpha and 49% for CFP, though the differences were not significant.

115 n heavy chain (aMHC) promoter and coding for CFP.

116 to monitor the A-N interdomain distance for CFP-SERCA selectively labeled with fluorescein isothiocy

117 CFP illness, and potential risk factors for CFP.

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

120 all 136 (100%) retinal regions selected for CFP and SDOCT grading.

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

126 We monitored the recruitment of GFP-/CFP-labeled signaling proteins by acquiring sequential i

127 Hence, CFP-10 may contribute specifically to neutrophil recruit

128 rculosis also harbors an encapsulin homolog (CFP-29, Mt-Enc), within an operon with M. tuberculosis D

129 e of a Src-mediated conformational change in CFP/YFP-tagged WT-Cav1 pairs.

130 A third epitope in CFP-10 was identified but exhibited promiscuous restrict

131 Two epitopes in CFP-10 were characterized, and the MHC class II alleles

132 come this issue, we amend the formulation in CFP, so as to account for atomic fate information.

133 However, mitochondria in CFP-LGP2:YFP-LGP2 cells had lower FRET signal in the pre

134 Mitochondria in CFP-RIG-I:YFP-RIG-I cells, CFP-MDA5:YFP-MDA5 cells, and

135 risk of problem shifting when reductions in CFP are obtained at the expense of increase in other env

136 When we introduced CFP and YFP separately in different NKCC1 constructs and

137 An isolated CFP-290-299 peptide remained in the nucleus in the prese

138 Macular CFP hyperpigmentation was significantly associated with

139 RET pair consists of CFPs and YFPs, but many CFP-YFP reporters suffer from low FRET dynamic range, ph

140 20 study eyes, which permitted double-masked CFP and SDOCT grading by certified investigators.

141 chemoattractant protein (MCP1) in mediating CFP recruitment/homing.

142 The minimal CFP-10 protein detection limit was 0.09 mug/mL.

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.

146 s using Poisson regression to relate monthly CFP call incidence to SST and tropical storms.

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

149 This application of CFP was possible because we discovered that O2-dependent

150 climate change could increase the burden of CFP.

151 80 with two copies of ESAT-6 and one copy of CFP-10 [SopE(Nt80)-E2C]) afforded protection against aer

152 -confirmed ciguatoxic meal remnants, cost of CFP illness, and potential risk factors for CFP.

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

156 We explored the incidence of CFP, percentage of CFP case-patients with laboratory-con

157 onnectivity of the pores and independence of CFP measurements with respect to capillary length.

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

160 Using CFP calls as a marker of CFP incidence, these results clarify associations betwee

161 An ITN mixture of CFP 100 mg/m(2)+alpha 25 mg/m(2) was compared with CFP 1

162 In experimental huts the mixture of CFP 100+ Alpha 25 killed 58% of An. arabiensis, compared

163 Tunnel tests showed that mixtures of CFP 100+ alpha 25 were 1.2 and 1.5 times more effective

164 FRET efficiency was detected in mixtures of CFP- and YFP-tagged full-length Kir6.2 subunits and tran

165 The number of CFP-positive retinal ganglion cells was quantified in re

166 Interestingly, overexpression of CFP-Hsc70 can induce muscular defects in wild-type nemat

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

170 Replacement of CFP and YFP with these two proteins in reporters of kina

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

174 the presence of advanced AMD not apparent on CFP.

175 For each eye, areas on CFP in which at least two of three retina specialists ag

176 e correlated with hyperpigmentary changes on CFP, versus two of 29 (6.9%) control regions (P < 0.001)

177 nvironmentally sensitive fluorescence dye on CFP-PAcKer adjacent to the binding site.

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

180 on for masked grading of regions selected on CFP and SDOCT.

181 ecretion via a C-terminal signal sequence on CFP-10 that is recognized by the cytosolic ATPase, Rv387

182 Although nGA is undetectable on CFP, it is important for determining the risk of future

183 t proteins in combination with the optimized CFP variant mTurquoise2 as the donor.

184 asciatus than either Alpha 25 (P = 0.001) or CFP 100 (P = 0.001) ITNs.

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

188 t, SERCA, we measured FRET from CFP-SERCA or CFP-PLB to YFP-PLB in live AAV-293 cells.

189 transfer (FRET) between STIM1-YFP and Orai1-CFP.

190 Co-expression of Orai1-CFP and Orai1-YFP results in a high degree of FRET in re

191 fter 2-APB addition, binding avidly to Orai1-CFP with a rapid increase in FRET and transiently increa

192 ch as C. elegans; however, a CXXC1 ortholog (CFP-1) is present.

193 el pathway concept termed carbon flux paths (CFPs) was introduced and benchmarked against existing ap

194 with the expression of PKCzeta-YFP and PDK1-CFP.

195 y transfer (FRET) from a circularly permuted CFP mutant to FlAsH, a selectively reactive fluorescein,

196 mentary changes on color fundus photographs (CFP) with abnormal morphology on SDOCT.

197 ofluorescence, and color fundus photographs (CFP).

198 review of digital color fundus photographs (CFPs).

199 e Study 2 (AREDS2) color fundus photography (CFP) grading.

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

202 rescence (FAF) and color fundus photography (CFP).

203 d retinal imaging (color fundus photography [CFP], spectral-domain [SD] optical coherence tomography

204 PLM-CFP also showed FRET to PLM-YFP, but the relationship du

205 r the synthesis of two copies of ESAT-6 plus CFP-10 fused to the OmpC signal sequence (OmpC(SS)-E2C)

206 Although ciguatera fish poisoning (CFP) is the most common seafood intoxication worldwide,

207 ed to incidence of ciguatera fish poisoning (CFP).

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

210 haracterized using capillary flow porometry (CFP) and scanning electron microscopy (SEM).

211 The estimated annual incidence of possible CFP was 4.0 per 1,000 person-years, and that of probable

212 odel that circulating fibroblast precursors (CFPs) are of HSC origin.

213 was possible with criteria used in previous CFP studies.

214 r genes, including ProHY5:HY5-GFP and Pro35S:CFP-PIF1, and various FR-HIR-dependent physiological res

215 per 1,000 person-years, and that of probable CFP was 7.5 per 1,000 person-years.

216 Case-fatality proportion (CFP) was higher among countries with systematic death re

217 The 10-kDa culture filtrate protein (CFP-10) and 6-kDa early secretory antigen of T cells (ES

218 AT-6) and a 10-kDa culture filtrate protein (CFP-10), that is essential for virulence.

219 enhanced cyan or yellow fluorescent protein (CFP or YFP, respectively).

220 r (FRET) pair, the cyan fluorescent protein (CFP) and yellow fluorescent protein (YFP).

221 sandwiched between cyan fluorescent protein (CFP) and yellow fluorescent protein (YFP).

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

227 xpressing stathmin-cyan fluorescent protein (CFP) or injected with stathmin protein.

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

230 Fusions of cyan fluorescent protein (CFP) to MldA, MldB, and MldC revealed that all three pro

231 re created to fuse cyan-fluorescent protein (CFP) to the N terminus of SERCA (A domain).

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

239 protein (YFP) and cyan fluorescent protein (CFP)-Ggamma(2).

240 o a loop in a host cyan fluorescent protein (CFP).

241 arrying a cyan fluorescent reporter protein (CFP) gene linked to the Thy-1 promoter, which expresses

242 DNA-HSP65 or CpG/culture filtrated proteins (CFP) immunotherapy.

243 Using httQ72-Luc with Q80(CFP/YFP) as seeds, we screened the Johns Hopkins Clinica

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

246 % compared to approximately 31% in a related CFP-Venus fusion.

247 odified the experimental system by replacing CFP with the SgrS small RNA, which regulates glucose and

248 onsumed barracuda were more likely to report CFP (p = 0.02).

249 gene turn on or off a fluorescent reporter (CFP).

250 t of 20 study eyes, 28 of 39 (71.8%) retinal CFP regions with hyperpigmentation were correlated with

251 The sensitive CFP/FlAsH FRET assay used here provides new insights int

252 ve in interphase; overexpression of stathmin-CFP did not impact metaphase microtubule nucleation rate

253 efficient secretion of the ESX-1 substrates CFP-10 and EspB.

254 Surprisingly, CFP-10 rather than ESAT-6 was responsible for triggering

255 Notably, for Syk-CFP we observed a rapid stimulated translocation to the

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

259 These data demonstrate that CFP-10 is a protective antigen and that CFP-10(32-39)-sp

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

263 The CFP and SD-OCT maps were compared and agreement was quan

264 The CFP measurements for monoliths prepared by the same proc

265 The CFP-10 and ESAT-6 antigenic regions targeted by T cells

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

268 The last reform of the CFP, in 2002, introduced effort control as part of more

269 Thus, the CFP/GFP ratio gives the effective c-di-GMP per biomass.

270 Further reforms to the CFP are currently being developed, so it is important, w

271 When integrated with the CFP/YFP pair, this new pair allowed the revelation of an

272 These CFP-10(32-39)-specific CD8+ cells undergo a rapid expans

273 This CFP-SERCA fluorescent fusion protein retained activity w

274 ating broad biological significance for this CFP/chemokine interaction.

275 Thy1-CFP expression was limited to retinal ganglion cell bodi

276 f the fluorescent retinal neurons in 30 Thy1-CFP mice were obtained using a modified confocal scannin

277 quantified in retinas of Ins2(Akita/+) Thy1-CFP mice.

278 e within fluorescent retinal neurons of Thy1-CFP mice after optic nerve crush.

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

281 (CFP)-fluorescent RGCs in the B6.Cg-Tg(Thy1-CFP)23Jrs/J mouse line.

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

285 ith a similar but nonsignificant response to CFP-10.

286 animals mounted similar T-cell responses to CFP-10 and ESAT-6.

287 identified that induced responses similar to CFP-10 and ESAT-6 in both magnitude and frequency.

288 fer pairs, one of which is the commonly used CFP-YFP pair, with a single-excitation laser line.

289 Using CFP calls as a marker of CFP incidence, these results cl

290 By using CFP only for SDD detection per the AREDS protocol, preva

291 interaction of YFP-tagged AKAP79(1-153) with CFP-tagged KCNQ2-5.

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

295 d was confirmed in living cells by FRET with CFP-Rac2 and YFP-PLD2 fluorescent chimeras.

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

299 A maximum YFP/CFP FRET ratio of 2.8 was observed in the presence of sa

300 In vitro measurements of YFP/CFP fluorescence emission ratios indicated that the addi