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 appears to induce the intracellular upregulation of

4 CFP-1 directly binds SIN-3 through a region including th

5 CFP-PAcKer binds more tightly to a full-length variant o

6 CFPs are simple paths in a metabolite-metabolite graph t

7 developed (each including age) based on: (1) CFP only (2 parameters); (2) OCT biomarkers, minimal (3

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

9 -6) protein and culture filtrate protein 10 (CFP-10) antigens via the Salmonella type III secretion s

10 aptured antigen is cell filtrate protein 10 (CFP-10) because its Mascot analysis shows a score of 68.

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

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

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

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

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

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

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

18 biomarkers, extended (7 parameters); and (4) CFP and OCT combined (8 parameters).

19 e with RASV strains synthesizing SopE-ESAT-6-CFP-10 fusion proteins resulted in significant protectio

20 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

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 yr-2801 in the cardiac RyR (RyR2) to yield a CFP- and YFP-dual labeled RyR2 (RyR2(Ser-2367-CFP/Tyr-28

28 cell line stably expressing alpha-syn (A53T)-CFP/YFP fusion proteins to detect alpha-syn seeds in bra

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 y, and share sequence features of ESAT-6 and CFP-10 of the Type VII Secretion System (T7SS) of Mycoba

33 N-TB Gold (In-Tube) system, using ESAT-6 and CFP-10 peptides, before determining the relative gene ex

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 FP-RIG-I cells, CFP-MDA5:YFP-MDA5 cells, and CFP-MDA5:YFP-LGP2 cells had higher FRET efficiencies in

38 polymer (NIP) was confirmed for CFL, CFD and CFP in standard solutions as well as in milk samples.

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

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

41 A third vector encoding non-fused CIP and CFP was also constructed.

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

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

44 1 had gradable lesion data from both FAF and CFP.

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

46 OCT and CFP images were graded independently for the presence of

47 ic curve, 1.0, compared with en face OCT and CFP, 0.9 (P = 0.04) and 0.88 (P = 0.025), respectively.

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

49 bility analysis for DF SLO, en face OCT, and CFP were 0.8, 0.71, and 0.67, respectively.

50 ltimodal imaging, including DF SLO, OCT, and CFP, was performed in 24 patients (24 eyes; 10 men and 1

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

52 OCT volume scans and CFP images were obtained from all participants at baseli

53 esults reveal good agreement between SEM and CFP measurements for through-pore size distribution.

54 gical activity of CFP-10 has been shown, and CFP-10 has been described as a chaperone protein for ESA

55 F SLO and en face OCT and between DF SLO and CFP for grader 1 was 0.89 and 0.95, respectively, and fo

56 associations between climate variability and CFP incidence and suggest that, all other things equal,

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

58 escence, whereas slightly augmenting YFP and CFP brightness.

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

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

61 Automated image analysis produced another CFP map.

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

63 ty in a previously identified antidepressant CFP.

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

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

66 Masked readers assessed CFP and FA.

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

68 This approach is termed atomic CFP (aCFP).

69 ntly greater than that of PEDOT/CFP and bare CFP electrodes.

70 ressed neovascularization [NV] at baseline), CFP may be sufficient at baseline and end-of-study visit

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

72 the purified biosensor enhanced FRET between CFP and YFP, consistent with heavy metal-induced folding

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

74 demic range of CFP, the relationship between CFP incidence and specific environmental conditions is u

75 uorescence resonance energy transfer between CFP-iNOS and beta-arrestin 2-YFP (but not beta-arrestin

76 d Severity Scale (score 0-5) using bilateral CFP.

77 fluorescent fusion proteins, AT1R-YFP and BK-CFP, displayed robust co-localized Forster resonance ene

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

79 138 of 984 eyes (14%) considered healthy by CFP, pathologic features were detectable by OCT, with 8.

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

81 ansfected with wild-type, Y14D, or Y14F Cav1-CFP and -YFP constructs that FRET efficiency was greater

82 alexin (CFX), cefazolin (CFL), cefoperazone (CFP), cloxacillin (CLO), dicloxacillin (DCL), oxacillin

83 Mitochondria in CFP-RIG-I:YFP-RIG-I cells, CFP-MDA5:YFP-MDA5 cells, and CFP-MDA5:YFP-LGP2 cells had

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

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

86 molecules (cephalexin (CFL) and cephapirin (CFP)), was prepared by non covalent molecular imprinting

87 R: C3 and C5; complement factor (CF) B, CFD, CFP, CFH and CFI of the AP; and C4 of the classical and

88 ng model was trained to detect RPD from CFP (CFP model).

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

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

91 ual, N- and C-termini-tagged APP constructs: CFP-APP-YFP [containing the fluorescent tags, cyan fluor

92 images were transferred to the corresponding CFP images.

93 erapy by showing that both DNA-HSP65 and CpG/CFP downregulated house dust mite-induced allergic airwa

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

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

96 1 allergen were treated with DNA-HSP65, CpG/CFP, or with adoptively transferred cells from immunized

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

98 ls from mice immunized with DNA-HSP65 or CpG/CFP to allergic recipients downmodulated the allergic re

99 ly, transfer of cells from DNA-HSP65- or CpG/CFP-immunized MyD88(-/-) mice failed to reduce allergy.

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

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

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

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

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

105 d direct link between Caenorhabditis elegans CFP-1 and an Rpd3/Sin3 small (SIN3S) histone deacetylase

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

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

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

109 as measured in millimeters squared from FAF, CFP, and IR images.

110 Participants underwent SD-OCT, FAF, CFP, and IR imaging at baseline and 12 months in the stu

111 aring both SD-OCT grading criteria with FAF, CFP, and IR, there were no statistically significant dif

112 rst, we identified a connectome fingerprint (CFP) in healthy participants (Cohort A, n = 25) during i

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 CFP illness, and potential risk factors for CFP.

116 The proportion of positive responders for CFP-10 and ESAT-6 between treatment arms was compared us

117 Our results reveal a novel role for CFP-1 in mediating interaction between SET1/COMPASS and

118 on, representing a novel biological role for CFP-10 in the ESAT-6:CFP-10 complex, beyond the previous

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

120 ions and the generation of quantitative FRET/CFP ratio images for both sensitized emission and spectr

121 earning model was trained to detect RPD from CFP (CFP model).

122 uorescently labeled at the N terminus (GAP43-CFP-Galphai/o) seem to faithfully reproduce the behavior

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

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

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

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

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

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

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

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

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

132 d using standardized protocols, and included CFP, multicolor imaging, fluorescein angiography, and in

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

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

135 d reproducibility of the discovered ketamine CFP in two separate healthy samples (Cohort B, n = 22; C

136 gnificant, robust, and reproducible ketamine CFP, consistent with reduced connectivity within the pri

137 Finally, we investigated the ketamine CFP connectivity at 1-week post treatment in major depre

138 Compared to placebo, the ketamine CFP connectivity changes at 1 week predicted response to

139 Macular CFP hyperpigmentation was significantly associated with

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

141 20 study eyes, which permitted double-masked CFP and SDOCT grading by certified investigators.

142 st-corrected visual acuity (VA) measurement, CFP, spectral-domain OCT, and OCT angiography (OCTA).

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

144 Results showed associations between monthly CFP calls and both warmer SSTs and increased tropical st

145 We estimated associations between monthly CFP incidence in the contiguous United States and SST an

146 strongest association linked current monthly CFP calls to the peak August SST of the previous year.

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

148 periments conducted using Nox1-YFP and NOXA1-CFP illustrate that NoxA1ds disrupts the binding interac

149 activities, no direct biological activity of CFP-10 has been shown, and CFP-10 has been described as

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

151 climate change could increase the burden of CFP.

152 80 with two copies of ESAT-6 and one copy of CFP-10 [SopE(Nt80)-E2C]) afforded protection against aer

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

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 tening late AMD as well as manual grading of CFP.

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

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

159 scent protein (CFP), emission intensities of CFP and YFP (yellow fluorescent protein) are captured be

160 as of disagreement underscore limitations of CFP-based measurement of drusen, particularly in the siz

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

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

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

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

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

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 ate change could expand the endemic range of CFP, the relationship between CFP incidence and specific

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

170 rd genetically encoded FRET pair consists of CFPs and YFPs, but many CFP-YFP reporters suffer from lo

171 roduced MCP1 inhibited in vitro migration of CFPs in response to multiple tumor types, indicating bro

172 the presence of advanced AMD not apparent on CFP.

173 elopment was similar for the models based on CFP alone (model 1; 0.80), OCT alone (models 2 and 3; 0.

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

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

176 ironmental management focused exclusively on CFP runs the risk of inadvertently shifting the problem

177 etion of natural resources, and the focus on CFP brings the risk of problem shifting when reductions

178 are visible on OCT, but are easily missed on CFP and clinical examination.

179 d one of them also showed visible pigment on CFP.

180 13 showed ORHR, of which 5 showed pigment on CFP.

181 often did not correspond to pigmentation on CFP.

182 lesions correlate well with features seen on CFP and ICGA.

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

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

185 e following features: lesion pigmentation on CFPs corresponding to hypoautofluorescent FAF (88% vs 0%

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

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

188 iters to ESAT-6 and production of ESAT-6- or CFP-10-specific gamma interferon (IFN-gamma)-secreting a

189 ns not identified by clinical examination or CFP are detectable with OCT.

190 f those had gradable lesion data from FAF or CFP, and 321 had gradable lesion data from both FAF and

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

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

193 ochemically deposited on carbon fiber paper (CFP) substrate modified with poly(3,4-ethylenedioxythiop

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

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

196 The electrocatalytic activity of Ir-PEDOT/CFP electrode towards oxidation of morin, a flavonoid wa

197 was significantly greater than that of PEDOT/CFP and bare CFP electrodes.

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

199 ed for classifying color fundus photographs (CFP) of individual eyes by AREDS severity score, none to

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

201 ofluorescence, and color fundus photographs (CFP).

202 rative analysis of color fundus photographs (CFPs), OCT, and FAF was performed for peripapillary and

203 re imaged with UWF color fundus photographs (CFPs), UWF FA, and SS-WF OCTA at baseline (M0) and 1 mon

204 review of digital color fundus photographs (CFPs).

205 s as determined by color fundus photography (CFP) and a validated grading system, we screened for pat

206 underwent OCT and color fundus photography (CFP) at baseline and were then reviewed at 6-month inter

207 without pigment on color fundus photography (CFP) at presentation were studied over a mean of 36.6 mo

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

209 phy should include color fundus photography (CFP), confocal fundus autofluorescence (FAF), confocal n

210 ectral-domain OCT, color fundus photography (CFP), near-infrared reflectance, and fundus autofluoresc

211 (GA) as defined on color fundus photography (CFP).

212 hese with standard color fundus photography (CFP).

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

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

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

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

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

218 an Union, where the Common Fisheries Policy (CFP) has been criticized for failing to protect stocks [

219 orm of the European Common Fisheries Policy (CFP), which intends to ban discards through the landing

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

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

222 was possible with criteria used in previous CFP studies.

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

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

225 ressive role of complement factor properdin (CFP) in vitro and in vivo.

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

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

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

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

230 fluorescent tags, cyan fluorescent protein (CFP) and yellow fluorescent protein (YFP)] and FLAG-APP-

231 thodology uses the cyan fluorescent protein (CFP) as a biomass indicator and the GFP as a c-di-GMP re

232 e linked to YFP or cyan fluorescent protein (CFP) at N or C termini, and all such constructs, includi

233 localization of a cyan fluorescent protein (CFP) fusion and a protein-protein interaction in Arabido

234 nations to express cyan fluorescent protein (CFP) or YFP fused to either biologically active HCV heli

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

236 Mice expressing cyan fluorescent protein (CFP) under control of the Thy-1 promoter received MS-275

237 droxylase 1 (Tph1)-cyan fluorescent protein (CFP), c-Kit(wsh/wsh), and Neurog3Cre;ROSA(tdTom) mice by

238 d-to-end fusion of cyan fluorescent protein (CFP), chicken metallothionein II (MT-II), and yellow flu

239 excitation of the cyan fluorescent protein (CFP), emission intensities of CFP and YFP (yellow fluore

240 ty is localized to cyan fluorescent protein (CFP)-fluorescent RGCs in the B6.Cg-Tg(Thy1-CFP)23Jrs/J m

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

242 Here, using cyan fluorescent protein (CFP)-tagged Fpn in conjunction with yellow fluorescent p

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

244 ing CIP fused with cyan-fluorescent-protein (CFP), with or without nuclear localization signal.

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

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

247 tors that did not express the CIP gene (rAAV-CFP-Neo) served as controls.

248 /rAAV-CIP, and more than 75% of rHSV48Y/rAAV-CFP-Neo co-infected cells were positive for both transge

249 show that in cultures co-infected with rAAV-CFP-Neo, 27% of the CFP-positive cells present rHSV48Y r

250 % compared to approximately 31% in a related CFP-Venus fusion.

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

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

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

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

255 on multicolor imaging differs from standard CFP, although the location and shape of lesions correlat

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

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

258 gher levels of blood-feeding inhibition than CFP alone for susceptible (94 vs 46%, P = 0.001) and res

259 des more biologically relevant pathways than CFP, because canonical pathways are more easily recovere

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 The CFP and ICGA images were independently graded by reading

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 model demonstrated substantially superior performanc

266 The CFP model showed equivalent values of 0.832 (95% CI, 0.8

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

268 y investigating the correlations between the CFP and 13 other impact scores, we show that some enviro

269 w FRET dynamic range, phototoxicity from the CFP excitation light and complex photokinetic events suc

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

271 es co-infected with rAAV-CFP-Neo, 27% of the CFP-positive cells present rHSV48Y replication compartme

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

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

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

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

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

277 in under control of the Thy-1 promoter (Thy1-CFP mice) to determine how the alpha2-adrenergic agonist

278 in under control of the Thy-1 promoter (Thy1-CFP mice) was imaged using a blue-light confocal scannin

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

280 = 0.09% versus 0.01%; p = 0.038) but also to CFP-10 (Fo = 0.16% versus 0.007%; p = 0.04) and staphylo

281 Using label transfer from FAF to CFP images, a deep learning model was trained to detect

282 on expression of tau or synuclein fusions to CFP and YFP, and confirmed its sensitivity and specifici

283 ere unique among leukocytes in responding to CFP-10, as monocytes and lymphocytes failed to produce a

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

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

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

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

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

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

290 ages were compared with those detected using CFP and ICGA.

291 Automated RPD detection using CFP achieved a lower accuracy that still surpassed that

292 icroaneurysms and retinal hemorrhages on UWF CFP at M3 versus M0 (n = 40+/-28 vs. 121+/-57; P = 0.002

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

294 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

295 measurements using FAF imaging compared with CFP, the measurements were highly correlated with one an

296 vK) of Escherichia coli K12 was flanked with CFP (cyan fluorescent protein) and YFP (yellow fluoresce

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

298 FRET between exchanger proteins tagged with CFP or YFP at position 266 within the large cytoplasmic

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