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1 ic organelles, F-actin, keratin, and soluble fluorescein.
2 rofiles red-shifted nearly 50 nm compared to fluorescein.
3 anaphylactic reaction after the injection of fluorescein.
4 f the laboratory analysis by the presence of fluorescein.
5 ating PM disruption and cytosolic release of fluorescein.
6 larizations collapsed after the injection of fluorescein.
7 d the interference of laboratory analyses by fluorescein.
8 oscopy to monitor BBB permeability of sodium fluorescein (376 Da), Alexa Fluor (643 Da), and fluoresc
10 mination including color fundus photography, fluorescein and indocyanine green angiographies, spectra
11 ecialists evaluated color fundus photographs fluorescein and indocyanine green angiography images to
12 n, fundoscopy, optical coherence tomography, fluorescein and indocyanine green angiography in a 66 ye
13 gs of tumor basal diameter and thickness and fluorescein and indocyanine green angiography were no di
14 est for color vision, quality of life (QoL), fluorescein and indocyanine green angiography, and optic
19 were first discovered in the 1800s, and the fluorescein and rhodamine scaffolds have been known for
21 n, and propranolol) and two model compounds (fluorescein and sulforhodamine B) from porous media foll
22 to existing methods using simulated spectra, Fluorescein and TAMRA dye mixtures as a zero FRET contro
24 tained for acetazolamide, riboflavin, sodium fluorescein, and theophylline in 2-hydroxyethyl methacry
25 ncreased by ~ 10% for a small solute, sodium fluorescein, and ~ 120% for larger solutes, BSA and Dex-
26 field testing, fundus photography (FP), OCT, fluorescein angiogram (FA), and fundus autofluorescence
30 of GA in digital color photographs (CPs) and fluorescein angiograms (FAs) taken at baseline and years
31 d vascular patterns than were visible on the fluorescein angiograms although within a more posterior
33 retinal periphery that were obscured in the fluorescein angiograms by fluorescein staining from unde
38 signal regions led to faster development of fluorescein angiographic patterns (3.1-fold; p = 0.02).
39 ns showed transient or persistently improved fluorescein angiographic signal (11.2-fold; p = 0.014).
41 All images from subjects with same-day UWF fluorescein angiography (FA) and color imaging were eval
44 V detection compared to the gold standard of fluorescein angiography (FA) and OCT was determined for
45 ting, refraction, dilated fundus examination fluorescein angiography (FA) and SD-OCT (spectral Domain
47 Patients were imaged longitudinally with fluorescein angiography (FA) and swept-source (SS) OCT a
49 CTA) was compared with ultrawide-field (UWF) fluorescein angiography (FA) for evaluating neovasculari
52 evaluated digital color fundus photographs, fluorescein angiography (FA) images, and optical coheren
53 ging was compared with ultra-widefield (UWF) fluorescein angiography (FA) imaging to better understan
56 cystoid macular edema (CME), and the highest fluorescein angiography (FA) score during the course of
62 c retinopathy (PDR) on ultra-widefield (UWF) fluorescein angiography (FA) were identified and compare
64 mic examination, OCT angiography (OCTA), and fluorescein angiography (FA) with widefield imaging.
65 examination including structural OCT, OCT-A, fluorescein angiography (FA), and indocyanine green angi
66 atients underwent SS OCT angiography (OCTA), fluorescein angiography (FA), and indocyanine green angi
67 ollow-up morphology on digital color images, fluorescein angiography (FA), and optical coherence tomo
69 ged with optical coherence tomography (OCT), fluorescein angiography (FA), blue fundus autofluorescen
71 uipment, including color fundus photography, fluorescein angiography (FA), OCT, and PAM, was used to
72 raphy, fundus photography, autofluorescence, fluorescein angiography (FA), optical coherence tomograp
79 studied using fundus imaging, SS-OCT, fundus fluorescein angiography (FFA), and indocyanine green ang
80 raphy (ERG), fundus photography (FP), fundus fluorescein angiography (FFA), and optical coherence tom
82 ical coherence tomography (OCT), intravenous fluorescein angiography (IVFA), indocyanine-green angiog
84 s with DR that had undergone ultra-widefield fluorescein angiography (UWFA) with associated color pho
85 inical study to determine if ultra-widefield fluorescein angiography (UWFA), spectral-domain optical
88 ing techniques, including widefield imaging, fluorescein angiography (with peripheral sweeps), and OC
93 Retinal perfusion status was evaluated by fluorescein angiography based on the presence or absence
94 a monthly basis with fundus photography and fluorescein angiography before and after each IAC inject
96 This information in combination with ICG and fluorescein angiography can help to optimize direct lase
100 An 86-year old Caucasian woman undergoing fluorescein angiography due to suspected peripapillary n
101 iography, indocyanine green angiography, and fluorescein angiography for comparison with the patholog
110 gonioscopy, dilated fundus examination, and fluorescein angiography is recommended in infants with s
112 us autofluorescence results, ultra-widefield fluorescein angiography results, and indocyanine green a
116 e large choroidal vessels and optic atrophy; fluorescein angiography revealed gradual restoration of
117 the anterior chamber (P = .007); the highest fluorescein angiography score (P = .011); age (P < 0.001
122 ts (n = 6 eyes of 3 patients) with widefield fluorescein angiography showed several retinal vascular
123 eld fundus imaging including pseudocolor and fluorescein angiography using an Optos 200Tx device.
128 ace between two domains (i.e. funduscopy and fluorescein angiography) provides an unrivaled way for t
130 cs, such as early onset, cuticular drusen on fluorescein angiography, and family history of AMD.
131 ocolor photography, fundus autofluorescence, fluorescein angiography, and indocyanine green angiograp
132 ocols, and included CFP, multicolor imaging, fluorescein angiography, and indocyanine green angiograp
133 domain OCT, autofluorescence imaging, fundus fluorescein angiography, and OCT angiography (OCTA) were
134 etails and images (color fundus photography, fluorescein angiography, and OCT) for all investigator-d
135 anibizumab, bevacizumab, fundus photographs, fluorescein angiography, and optical coherence tomograph
136 r pigment (MP), OCT, blue light reflectance, fluorescein angiography, as well as fundus photography,
137 had multimodal imaging (fundus photography, fluorescein angiography, autofluorescence, and spectral-
140 in all patients and were hyperfluorescent on fluorescein angiography, hypofluorescent on ICG angiogra
141 e were imaged with autofluorescence imaging, fluorescein angiography, indocyanine green angiography,
142 h various combinations of color photography, fluorescein angiography, indocyanine green angiography,
143 omplete ophthalmologic examination including fluorescein angiography, indocyanine green angiography,
144 methods such as enhanced depth imaging-OCT, fluorescein angiography, indocyanine green angiography,
145 erwent indocyanine green angiography, fundus fluorescein angiography, mesopic microperimetry, and mul
146 as identified on dilated fundus examination, fluorescein angiography, or both in 11 eyes of 6 patient
148 graphy, fundus autofluorescence, intravenous fluorescein angiography, spectral-domain OCT and OCT ang
149 gathering included fundus color photographs, fluorescein angiography, spectral-domain optical coheren
150 ging findings, including fundus photography, fluorescein angiography, spectral-domain optical coheren
152 ion when choosing the healthcare setting for fluorescein angiography, such as the immediate availabil
153 uate retinal capillary blood flow instead of fluorescein angiography, the reflectance pattern of bloo
164 (SD OCT), fundus autofluorescence (FAF), and fluorescein angiography/indocyanine green (ICG) angiogra
167 , we developed sensitive assays that use the fluorescein arsenical dye FlAsH (fluorescein arsenical h
168 nergy transfer (FRET) approach using a small fluorescein arsenical hairpin (FlAsH) targeted to a shor
169 hat use the fluorescein arsenical dye FlAsH (fluorescein arsenical hairpin binder) to detect soluble
170 To overcome this limitation, we develop the Fluorescein Arsenical Hairpin Binder- (FlAsH-) based FRE
171 rgy transfer (BRET)-based and conformational fluorescein arsenical hairpin-BRET sensors coupled with
176 nt a new family of readily functionalizable, fluorescein-based voltage-sensitive fluorescent dyes (sa
177 dation of dihydrorhodamine 123, AAPH-induced fluorescein bleaching and hypochlorite-induced fluoresce
180 criptase quantitative PCR and measurement of fluorescein concentrations (doped into the nebulized aer
182 ss the capillary bed with the small molecule fluorescein, concomitant with reactive astrocytosis.
183 adhesive-dentin interface were covered with fluorescein-conjugated gelatin and observed with a multi
184 nhibited (40-70% inhibition) the cleavage of fluorescein-conjugated gelatin by MMP-2, but not MMP-9.
185 Fluorescence intensity emitted by hydrolyzed fluorescein-conjugated gelatin was quantified, and the a
187 r "ELISA"), to small molecule ligands, using fluorescein conjugates and antifluorescein antibodies as
190 ctive tests: tear film break-up time (TBUT), fluorescein corneal staining (FL/S) and Schirmer test.
191 0 induced an increase in the fluorescence of fluorescein diacetate (FDA) by 30 and 42%, suggesting a
193 ha were measured as proliferation by carboxy-fluorescein diacetate succinimidyl ester dye dilution an
194 esophageal stent to demonstrate delivery of fluorescein diacetate, using applied tension, to an ex v
197 a detection limit of 613 +/- 13 pM for CE of fluorescein disodium salt solution in borate buffer.
198 e Suzuki cross-coupling of the electron-poor fluorescein ditriflate with the electron-rich boronic ac
200 alized with two different dyes, respectively fluorescein (donor) and eosin (acceptor), which form a s
201 itoring the enzymatic cohydrolysis of FDL to fluorescein during enzymatic hydrolysis of the polyester
206 n of single stranded DNA labeled with either fluorescein (FAM) or tetramethylrhodamine (TAMRA) with a
208 e of three model compounds, ibuprofen (IBU), fluorescein (FLU), and 4',6-diamidino-2-phenylindole (DA
210 ophthalmoscopy, color fundus photography and fluorescein fundus angiography, before and immediately a
211 t an interference with laboratory testing by fluorescein in this patient and summarize the literature
213 el was evaluated using a fluorescent tracer (fluorescein) incorporated in the carrier materials calci
216 d directly at the valve outlet by monitoring fluorescein injection profiles with laser-induced fluore
218 the dyes in their free isothiocyanate forms, fluorescein isothiocyanate (F-ITC) and tetramethylrhodam
219 arch on feasibility, removal of unconjugated fluorescein isothiocyanate (FITC) after fluorescent labe
220 oring of the bioconjugation reaction between fluorescein isothiocyanate (FITC) and a model protein il
222 ing of the film, after a post-treatment with Fluorescein Isothiocyanate (FITC) labeled 8-OHdG antibod
223 reened for their ability to inhibit anti-CR3-fluorescein isothiocyanate (FITC) staining of human neut
224 permeability, as measured by the passage of fluorescein isothiocyanate (FITC)-dextran through endoth
225 d DSS plus ATB (DSS+ATB) was demonstrated by fluorescein isothiocyanate (FITC)-dextran translocation
228 ching technique, diffusion coefficients D of fluorescein isothiocyanate (FITC)-pepsin were measured i
230 ocyanate-labeled IAV in the presence of anti-fluorescein isothiocyanate antibody also resulted in vir
232 r PEG-like molecules (CH3-PEG5K-FITC (FITC = fluorescein isothiocyanate) and eight-arm PEG20K-FITC) w
233 smural sections of jejunum were stained with fluorescein isothiocyanate-conjugated isolectin-B4 for e
234 ectrical resistance and paracellular flux of fluorescein isothiocyanate-dextran (4 kDa) together with
235 electrical resistance, paracellular flux of fluorescein isothiocyanate-dextran 4 kDa, and mRNA expre
236 sed intestinal permeability, as indicated by fluorescein isothiocyanate-dextran absorption and serum
238 Intestinal permeability was investigated by fluorescein isothiocyanate-dextran uptake assay, quantit
239 istance), reduced paracellular permeability (fluorescein isothiocyanate-dextran), and prevented vascu
240 by jugular vein infusion of (125)I-fibrin or fluorescein isothiocyanate-fibrin labeled emboli in anes
241 vascular permeability to Evans blue dye and fluorescein isothiocyanate-labeled bovine serum albumin
242 ransepithelial electrical resistance (TEER), fluorescein isothiocyanate-labeled dextran 4kDa (FD4) fl
244 4) was determined by co-immunoprecipitation, fluorescein isothiocyanate-probing, and surface plasmon
245 on revealed the specific binding capacity of fluorescein isothiocyanate-RamAb to VEGFR-2, and no diff
247 nscription during mitosis, as confirmed with fluorescein isothiocyanate-uridine 5'-triphosphate label
248 molecule Rhodamine B (RhB) and model protein Fluorescein isothiocynate (FITC) Bovine Serum Albumin (B
250 y high-affinity binding to standby-competent fluorescein-labeled +42 mRNA, but not to mRNAs that lack
251 uent was continuously contacted with soluble fluorescein-labeled Fc-binding ligands to produce an imm
252 completely, thereby conferring protection to fluorescein-labeled Micrococcus lysodeikticus from lysoz
254 the emission spectra of eosin (tetrabromine fluorescein) lake mixed with lead or zinc white at lower
258 eight bispecific adapters, each comprised of fluorescein linked to a different tumor-specific ligand,
259 skin burn severity using a topically applied fluorescein-loaded liquid bandage and an unmodified comm
260 conjugation and delivery of the model probe fluorescein-maleimide and the medicinal agent paclitaxel
261 ated by impregnating 2.5 muL (0.285 nmol) of fluorescein mercury acetate (FMA) onto the surface of a
262 the low molecular weight fluorophore sodium fluorescein (NaFl), whereas diet-induced insulin resista
263 owed previously undescribed features such as fluorescein-negative intraretinal cystic changes, choroi
264 as assessed using CaSO4 beads that contained fluorescein or antibiotics and were pre-coated with huma
267 Following incubation of L929 cells with fluorescein PMs, there was a gradual increase in intrace
268 concentration had no influence on short-term fluorescein release and pre-coating of beads with body f
269 scent guests, namely coumarin 1, coumarin 4, fluorescein, [Ru(bpy)3 ]Cl2 , and rhodamine B, can be en
273 s -1.14 +/- 1.68 seconds, P < .001), corneal fluorescein staining (-0.62 +/- 0.30 vs 0.19 +/- 0.37, P
275 The main efficacy end points were corneal fluorescein staining (CFS), tear film break-up time (TBU
276 outcome at 3 months and limbal conjunctival fluorescein staining (r = 0.67, P = .006), and limbal co
277 re obscured in the fluorescein angiograms by fluorescein staining from underlying, preexisting laser
278 ed healing status conventionally (<0.5 mm of fluorescein staining in the greatest dimension of the le
279 reases in the postoperative LG scores and in fluorescein staining post ptosis surgery compared with t
280 thout anesthesia) >/=1 and </=10 mm, corneal fluorescein staining score >/=2.0 (0-4 scale), eye dryne
282 infiltration of Th17 cells and lower corneal fluorescein staining scores compared with saline-treated
283 points including total and subregion corneal fluorescein staining, conjunctival staining, visual anal
284 Schirmer test 2, tear break-up time (TBUT), fluorescein staining, Lissamine-green staining (LG).
285 045) but not with tear breakup time, corneal fluorescein staining, or ocular medications used by pati
286 underwent clinical examination with corneal fluorescein staining, Schirmer 1 tear test, assessment o
287 ondrial membrane potential readings, corneal fluorescein staining, tear volume concentrations, tear f
288 ependent assays (CD154 detection and carboxy-fluorescein succinimidyl ester dilution assays) and 9 in
289 d by fluorescence polarization analysis of a fluorescein-tagged peptide corresponding to pol beta res
293 novel chemical probes, ubiquitin C-terminal fluorescein thioesters UbMES and UbFluor, to qualitative
297 al reduction of a quinone in the presence of fluorescein was selected to both generate and monitor a
298 the working principle for the model compound fluorescein, where the organic solvent DMSO is exchanged
299 terns at the 3' and 6' positions, similar to fluorescein, while simultaneously possessing excitation
300 tamol, ibuprofen, tamoxifen, BAY 11-7082 and fluorescein, with accuracy on the scale of micrograms pe