ライフサイエンスコーパス: FAST

1 FAST >0.35 remained an independent predictor of liver-re

2 FAST and CT contribute to triage, guide surgical managem

3 FAST and CT scans undertaken by attending radiologists c

4 FAST and E-FAST that are performed by experts tend to be

5 FAST enables complete visualization of the brain at a re

6 FAST examinations were performed in 1540 patients (1227

7 FAST examinations were performed on patients with precor

8 FAST is a positionally conserved lncRNA but is not conse

9 FAST is easy to adapt for any scanning microscope; its b

10 FAST mice were more sensitive to the stimulant effects o

11 FAST mice were more stimulated than SLOW mice by all dru

12 FAST proteins are the smallest viral membrane fusion pro

13 FAST proteins offer a minimalist model to better underst

14 FAST renders unbiased quantitative group comparisons of

15 FAST requires no prior information about the sample, is

16 FAST score predicts liver-related outcomes and can help

17 FAST therefore enables high-throughput, data-rich analys

18 FAST was inadequate in 3.7%, 28.9% demonstrated cardiac

19 FAST(-/-) mice develop airway inflammation that is disti

20 FAST(M) is also suited for multiplexing using single-cel

21 FAST-1 has been shown to associate with Smad2 and Smad4,

22 FAST-1 recognition of the ARE is essential both for ARF

23 FAST-2 also interacts directly with Smad2, a cytoplasmic

24 FAST-Forward is a multicentre, phase 3, randomised, non-

25 FAST-PB enables genome editing and product characterizat

26 FAST-PETase can also depolymerize untreated, amorphous p

27 FAST-PETase is one of the best enzymes hitherto proposed

28 FAST-PLVs show low immunogenicity and maintain activity

29 actor fork head activin signal transducer 1 (FAST-1) was identified as a mediator of activin signalin

30 teractive Thresholding Algorithm [SITA] 24-2 FAST), in a single sitting, using standardized clinical

31 racy and AUC compared with FibroScan, FIB-4, FAST, and NFS.

32 Five trauma surgeons performed 546 FAST examinations during the study period.

33 NIRF reporter of MMP activity (MMPSense-645-FAST), both probes produced statistically significant in

34 A FAST examination including parasternal/subxiphoid cardia

35 ons with the translational silencer TIA-1: a FAST mutant lacking its TIA-1-binding domain does not in

36 hose patients not referred to colonoscopy, a FAST Score < 2.12 allows to determine a group of patient

37 ompleting subsequent bowel investigations: a FAST score > 2.12 was found in 13 of 15 (86.7%) with SBD

38 Conversely, expression of a FAST-1-repressor fusion (FAST-En(R)) in prospective ecto

39 Using a FAST score > 2.12, which gives high clinical sensitivity

40 ions of complete, high-quality, and accurate FAST and E-FAST studies for children after injury.

41 ectopic expression of mutationally activated FAST-1, ectopic expression of dominant inhibitory FAST-1

42 n of constitutively transcriptionally active FAST-1 fusion protein (FAST-VP16(A)) in prospective ecto

43 4-2, Swedish Interactive Threshold Algorithm FAST).

44 All FAST interpretations were validated by at least one of f

45 Altogether, FAST(M) opens new opportunities for interrogating cellul

46 Analysis of the sequences of FAST-1 and FAST-2 reveals substantial protein sequence divergence c

47 urated hydrocarbon chains (e.g. DiIC(12) and FAST DiI) enter the endocytic recycling compartment effi

48 rdial Infarction (FAST-MI) 2005 (n=3670) and FAST-MI 2010 (n=4169).

49 fluorescent intermediate compounds (FIC) and FAST index, indicating the least MRP formation.

50 del with the STA/LTA, template matching, and FAST algorithms.

51 iewed the complete AP (consisting of MIP and FAST images and optionally their nonsubtracted source im

52 dihexadecyloxacarbocyanine perchlorate) and FAST DiO (3, 3'-dilinoleyloxacarbocyanine perchlorate) b

53 etramethylindocarbocyanine perchlorate), and FAST DiI (1,1'-dilinoleyl-3,3,3', 3'-tetramethylindocarb

54 method outperforms prior tools (QuSHAPE and FAST) significantly in terms of accuracy compared with g

55 The qualitative FAST results and FAST-derived MIC (MICFAST) correspond closely with broth

56 ty of Smad4 to form a complex with Smad2 and FAST on the Mix.2 promoter.

57 ferent from present multiplexing approaches, FAST(M) uses phase-sensitive signal detection, which ren

58 potential survivors after traumatic arrest, FAST represents an effective method of separating those

59 ncing technology in combination with the ASF-FAST software for the purpose of rapid and real-time res

60 ine fever fast analysis sequencing tool (ASF-FAST), the analysis of output data was performed in real

61 risk MASH and compared to the FibroScan-AST (FAST) score.

62 Because FAST is released from mitochondria in cells undergoing F

63 Because FAST(-/-) neutrophils exhibit normal chemotaxis and surv

64 have mapped the site of interaction between FAST-1 and Smad2/Smad4 to a novel carboxy-terminal domai

65 hroughput pipeline for plant bioengineering (FAST-PB) in maize (Zea mays) and Nicotiana benthamiana.

66 Both FAST and TIA1 are also found in the nucleus, where TIA1

67 Both FAST and TIA1 target a U-rich intronic sequence (IAS1) a

68 Both FAST-1 and Smads can bind directly to the ARE; we have i

69 We find that ARF binds to ARE through both FAST-1 and Smad binding sites.

70 carboxylase was decreased with CARB vs. both FAST (-0.7 +/- 0.6 fold, P = 0.04) and NIACIN (-1.0 +/-

71 lated Akt phosphorylation were unaffected by FAST versus BFAST in both lean and obese cohorts (all P

72 ytic acid but higher protein, iron, calcium, FAST index.

73 We find that this gene, which we call FAST-2, is able to mediate transcriptional activation by

74 of different NSP1-1 proteins and of chimeric FAST proteins suggest a potential role for rotavirus FAS

75 as important and appropriate for a complete FAST: right upper-quadrant abdominal view, left upper-qu

76 In conclusion, FAST allows for high-throughput data processing to match

77 Conversely, FAST did not predict extrahepatic events.

78 Towards this goal, we have developed FAST-DOSE (Fluorescent Automated Screening Tool for Dosi

79 In obese individuals, no differential (FAST versus BFAST) expression was observed in genes invo

80 ld either rotated in the opposite direction (FAST) or was unaltered (NATURAL).

81 nhancer in the mouse nodal gene, and directs FAST site-dependent expression in the primitive streak d

82 , we report that an evolutionarily divergent FAST protein, p22 from aquareovirus, also hijacks the ac

83 plete, high-quality, and accurate FAST and E-FAST studies for children after injury.

84 Consensus was reached on FAST and E-FAST study definitions, and the panelists rated these 5

85 FAST and E-FAST that are performed by experts tend to be more compl

86 Diagnostic workup associating E-FAST (including abdominal, thoracic, pubic, and transcra

87 For E-FAST, the same FAST anatomic views with the addition of

88 ed from an erroneous interpretation of the E-FAST.

89 nterference-mediated knockdown of endogenous FAST results in apoptosis, whereas overexpressed recombi

90 Among these, the engineered FAST-PETase variant exhibits superior catalytic efficien

91 The exWHO-FAST assay is an expanded redesign of the WHO-recommende

92 lar to the FFABR assay LODs, while the exWHO-FAST LODs were higher for two H3N2 strains, findings tha

93 the maternally encoded transcription factor FAST-1 in the establishment of the mesodermal transcript

94 and TGF-beta through Smads and the WH factor FAST-2.

95 , and a novel forkhead transcription factor, FAST-1, and binds to an enhancer (activin-responsive ele

96 temporally restricted transcription factor, FAST-1.

97 tion by a winged-helix transcription factor, FAST-2, on an activin-responsive element (ARE) in the Xe

98 before and after 6 weeks of morning fasting (FAST; 0 kcal until 12.00 h) or daily breakfast consumpti

99 The FFR(angio) Accuracy versus Standard FFR (FAST-FFR) study is a prospective, multicenter, internati

100 4 for a cutoff of > or =6 points vs 0.51 for FAST stage 7c).

101 records to determine diagnostic accuracy for FAST and CT and their influence on casualty management.

102 ted by the same domain which is required for FAST-2 to interact with Smad2.

103 se element, a high-affinity binding site for FAST-1.

104 njection of a blocking antibody specific for FAST-1 prevents induction of mesodermal response genes b

105 njection of a blocking antibody specific for FAST-1.

106 the winged-helix transcription factor FoxH1 (FAST), a critical component of a positive feedback loop

107 nd TATA box as well as potential Smad, FoxH1/FAST, T-box, COUP-TF, C/EBP, GATA, HNF3 binding sites an

108 of 17 individual QIs could be assessed from FAST-MI 2010.

109 term storage the modest changes in furosine, FAST index and browning in ginger cake formulated with d

110 Furthermore, FAST is highly scalable to non-human primate brains and

111 ly, expression of a FAST-1-repressor fusion (FAST-En(R)) in prospective ectoderm blocks induction of

112 f-Hb < 10 mug Hb/g faeces, 1371 (53.7%) had FAST score >= 2.12: clinical rationale led to only 122 o

113 s of the National Institute of Mental Health FAST-FAIL initiative, we were the first to show that, in

114 Mice selectively bred for high (FAST) or low (SLOW) locomotor stimulant response to etha

115 ly characterized to associate with the human FAST-1 protein.

116 Consistent with this hypothesis, FAST promotes the expression of cotransfected reporter p

117 embryonic tissue explant assays, identifying FAST as an essential mediator of Xnr autoregulation and/

118 In FAST-MI 2010, 12 individual and 2 composite QIs could be

119 ity to allopregnanolone was also measured in FAST and SLOW mice, which were selectively bred for diff

120 Four QIs were not recorded in FAST-MI 2010 and 4 in 2005, either because of treatment

121 eutrophil recruitment is markedly reduced in FAST(-/-) mice compared with wild type controls.

122 n or Non-ST-Elevation Myocardial Infarction (FAST-MI) 2005 (n=3670) and FAST-MI 2010 (n=4169).

123 n or Non-ST Elevation Myocardial Infarction (FAST-MI) 2005 according to use and type of reperfusion t

124 1, ectopic expression of dominant inhibitory FAST-1, and injection of a blocking antibody specific fo

125 For detection of intra-abdominal injury, FAST sensitivity (Sn) was 0.56, specificity (Sp) 0.98, p

126 In conclusion, our results introduce FAST as a proinflammatory factor that modulates the func

127 he principal DNA-binding component of ARF is FAST-1, a transcription factor with a novel winged-helix

128 LDTs and two were subtyped as H3 by the LDT-FAST assay only.

129 The LDT-FAST assay uses proprietary primers and probes designed

130 The LDT-FAST LODs were similar to the FFABR assay LODs, while th

131 SPM's alternative pre-whitening method, FAST, performed better than SPM's default.

132 describe a high-throughput NMR methodology (FAST-NMR) to annotate the biological function of novel p

133 Compared to existing methods, FAST imposes fewer distribution assumptions, utilizes th

134 eonine phosphoprotein (FAST)-deficient mice (FAST(-/-)) to study the in vivo role of FAST in immune s

135 The lowest fluorescence of advanced MRP (FAST) index was observed for buckwheat roasted at 130 de

136 requency- and spectrally-tuned multiplexing (FAST(M)).

137 speed serial-sectioning imaging system named FAST (block-face serial microscopy tomography), which ac

138 l injury; 26 (17%) of whom also had negative FAST studies.

139 Our data reveal that nuclear FAST can regulate the splicing of FGFR2 transcripts.

140 In a gel shift assay, the association of FAST-2 with Smad4 was mutually exclusive from the associ

141 The combination of FAST enrichment and ADM imaging has the performance requ

142 ognition of the ARE, 2) the contributions of FAST-1 and Smad binding to ARF binding in vitro and to A

143 /Smad4 to a novel carboxy-terminal domain of FAST-1, and find that overexpression of this domain spec

144 The antiapoptotic effects of FAST are regulated by interactions with the translationa

145 Because the antiapoptotic effects of FAST require ongoing protein synthesis, we hypothesized

146 ng is separable from the survival effects of FAST.

147 TIA-1 inhibits the antiapoptotic effects of FAST.

148 dermal genes by activin, while expression of FAST-En(R) in intact embryos prevents general/dorsal mes

149 Furthermore, the interaction of FAST-2 with BF-1 is mediated by the same domain which is

150 show that the exceptional time resolution of FAST(M) also allows resolving rapid chemical reactions.

151 ice (FAST(-/-)) to study the in vivo role of FAST in immune system function.

152 the ARE; we have investigated 1) the role of FAST-1 and Smad DNA binding sites in ARF recognition of

153 Analysis of the sequences of FAST-1 and FAST-2 reveals substantial protein sequence d

154 surgeons who are newly trained in the use of FAST can achieve an overall accuracy rate of at least 90

155 ED following blunt torso trauma, the use of FAST compared with standard care only did not improve cl

156 e findings do not support the routine use of FAST in this setting.

157 The authors also report on the utility of FAST in special patient populations, such as pediatric a

158 bdominal visceral injury limits the value of FAST as a screening diagnostic modality for patients who

159 abeled IgG and bovine serum albumin (BSA) on FAST, Unisart, and Oncyte-Avid slides and compared the s

160 x and that this association was dependent on FAST-2.

161 Cardiac motion on FAST was 100% sensitive and 73.7% specific for the ident

162 Consensus was reached on FAST and E-FAST study definitions, and the panelists rat

163 raphic examination of the trauma patient, or FAST, is replacing central venous pressure measurements

164 d, appropriate, specific and transparent (or FAST) will help to develop a thriving culture for review

165 Like some other FAST proteins, RVB NSP1-1 is predicted to have an N-term

166 the cytosolic tail of reptilian reovirus p14 FAST protein functions as a novel tribasic Golgi export

167 on factor SARA and the nuclear Smad2 partner FAST-1 for binding to a hydrophobic corridor on the MH2

168 Eligible adults had a PEN-FAST score lower than 3.

169 s-activated serine/threonine phosphoprotein (FAST) is a survival protein that is tethered to the oute

170 s-activated serine/threonine phosphoprotein (FAST) is tethered to the outer mitochondrial membrane, w

171 s-activated serine threonine phosphoprotein (FAST)-deficient mice (FAST(-/-)) to study the in vivo ro

172 ohydrate (CARB), niacin (NIACIN) or placebo (FAST) in a crossover design (11 +/- 6 days washout).

173 : 286 of 296 (96.6%) with SBD had a positive FAST score, as did 857 of 1151 (74.5%) without SBD.

174 NA binding partner, the winged helix protein FAST-1.

175 nscriptionally active FAST-1 fusion protein (FAST-VP16(A)) in prospective ectoderm can directly induc

176 Further, the observation that all putative FAST proteins tested can induce syncytium formation in a

177 The qualitative FAST results and FAST-derived MIC (MICFAST) correspond c

178 In contrast, r-FAST and r-SLOW mice differed in sensitivity to only a f

179 lar in sensitivity to ethanol stimulation (r-FAST and r-SLOW) and provided a unique model for testing

180 More compellingly, recombinant FAST increases the expression of endogenous cIAP-1 and X

181 apoptosis, whereas overexpressed recombinant FAST inhibits Fas- and UV-induced apoptosis, indicating

182 teins suggest a potential role for rotavirus FAST proteins in determining the efficiency of viral rep

183 For E-FAST, the same FAST anatomic views with the addition of the lung or pne

184 the published f-Hb, age and sex test score (FAST score) added value.

185 f abdominal free fluid and the use of serial FAST.

186 have also demonstrated the ability of SHAPE/FAST to detect the binding of a small molecule inhibitor

187 t Smad4 stabilizes a ligand-stimulated Smad2-FAST-1 complex as an active DNA-binding factor.

188 n, Smad4 promotes binding of the Smad2/Smad4/FAST-1 complex to DNA; through its carboxy-terminal doma

189 ortex and the Functional Assessment Staging (FAST) measure of the clinical severity of AD at the time

190 of 7c on the Functional Assessment Staging (FAST) scale.

191 In cells subjected to environmental stress, FAST moves to stress granules, where it interacts with T

192 rived images (first postcontrast subtracted [FAST] and maximum-intensity projection [MIP] images), wa

193 ence-activating and absorption shifting tag (FAST) that are compatible with two-color, live-cell imag

194 alline fluorinated aryl sulfonimide-tagged ("FAST") anion monomers.

195 a novel laterally elastic kinesiology tape (FAST, FS).

196 We call this technique FAST CARS (femtosecond adaptive spectroscopic techniques

197 ) and fiber-optic array scanning technology (FAST) to identify and image cells expressing HIV Gag.

198 uses fiber-optic array scanning technology (FAST), which applies laser-printing techniques to the ra

199 ed the faecal haemoglobin, age and sex test (FAST) score in the assessment of patients with lower bow

200 flow cytometry-assisted susceptibility test (FAST) method combines rapid qualitative susceptible/non-

201 eport that Smad4 is present in ARF, and that FAST-1, Smad4 and Smad2 co-immunoprecipitate in a ligand

202 complementary approaches to demonstrate that FAST-1 is a central regulator of mesoderm induction by e

203 d inhibit axis formation, demonstrating that FAST-1 is a necessary component of the first steps in th

204 The finding that FAST is concentrated at nuclear speckles also supports t

205 oing protein synthesis, we hypothesized that FAST might function by preventing TIA-1-mediated silenci

206 s- and UV-induced apoptosis, indicating that FAST is a survival protein.

207 as- or UV-induced apoptosis, we propose that FAST serves as a sensor of mitochondrial stress that mod

208 prisingly, knockdown experiments reveal that FAST and TIA1 act independently of one another to promot

209 screens and biochemical analysis reveal that FAST binds to several alternative and constitutive splic

210 that uses cell position alone revealed that FAST produced 4 to 10 fold fewer tracking errors.

211 Mutational analysis reveals that FAST-mediated alternative splicing is separable from the

212 We show that FAST, like TIA1, promotes the inclusion of exon IIIb of

213 Extensive simulation studies have shown that FAST outperforms other existing reference-free methods.

214 itutive splicing regulators, suggesting that FAST might participate in this process.

215 This suggests that FAST-2 represents a new WH gene related to FAST-1, which

216 The FAST cassette is similar in an ascidian nodal-related ge

217 The FAST is a rapid test that sequentially surveys the peric

218 The FAST package includes C++ implementations of various alg

219 The FAST score was assessed in both groups.

220 The FAST Trial (CRUKE/04/015) evaluated normal tissue effect

221 The FAST-1/Smad2/Smad4 complex binds and activates a 50 bp a

222 Although the FAST exam is not recommended as the sole screening tool

223 In a yeast two-hybrid assay, the FAST-1 carboxy terminus interacts with Smad2 but not Sma

224 patients experiencing HAE attacks during the FAST-2 open-label extension (OLE) phase.

225 Authors evaluated the FAST score threshold with a 99% sensitivity (>= 2.12) fo

226 of the liquid droplet was comparable for the FAST and Unisart slides but different, i.e., slower, for

227 To address this, we present here the FAST package, an open-source collection of programs and

228 To determine if the FAST examination during initial evaluation of injured ch

229 Median hospital charges were $46415 in the FAST group and $47759 in the standard care-only group (d

230 minal CT scans was 241 of 460 (52.4%) in the FAST group and 254 of 465 (54.6%) in the standard care-o

231 mean ED length of stay was 6.03 hours in the FAST group and 6.07 hours in the standard care-only grou

232 bdominal injury occurred in a patient in the FAST group and none in the control group (difference, 0.

233 valuable patients with cSSSI enrolled in the FAST II trial from 11 sites in the United States (56 iso

234 DESIGN, SETTING, AND PARTICIPANTS: In the FAST-01 nonrandomized trial, participants treated at Cin

235 art review will discuss the evolution of the FAST examination to its current state in 2017 and evalua

236 ermore, our data suggest that members of the FAST kinase domain-containing protein family are respons

237 The performance characteristics of the FAST score did not seem to enhance the utility of f-Hb a

238 Deletion mutants of the FAST-1 carboxy terminus that still participate in ligand

239 We have also examined the structure of the FAST-2 gene and find that it overlaps with a kinesin mot

240 study was to examine the performance of the FAST-DOSE assay system to quantify intracellular protein

241 Here, we present 5-year results of the FAST-Forward trial.

242 s was nonhomogenous and doughnut-like on the FAST and Unisart nitrocellulose slides, whereas a better

243 In the Hu-NSG mice studies, the FAST-DOSE biomarker panel was able to generate delivered

244 These results suggest that the FAST-DOSE bioassay has large potential as a useful diagn

245 ive icatibant-treated attacks throughout the FAST-2 OLE phase.

246 L1/ETO, contains a region of homology to the FAST proteins, which cooperate with Smads to regulate tr

247 Today the FAST examination has evolved into a more comprehensive s

248 hin 4 h of ICH onset; a phase III trial (the FAST trial) is now in progress.

249 This method used the FAST PCR technology and allowed a further reduction in t

250 The clinical conditions in which the FAST is most accurate in the assessment of injured patie

251 ned to a standard trauma evaluation with the FAST examination by the treating ED physician or a stand

252 nd that Smad3 was able to associate with the FAST-2.ARE complex and that this association was depende

253 was also able to directly associate with the FAST-2.ARE complex through binding with FAST-2.

254 y's Facile Accelerated Specific Therapeutic (FAST) platform to create antisense peptide nucleic acids

255 Intron 1 contains three FAST binding sites on which FAST/Smad transcriptional co

256 alone was able to stimulate the ARE through FAST-2, but inhibited the ARE transactivation mediated b

257 Thus, FAST provides new opportunities for global approaches th

258 However, unlike TIA1, FAST does not bind to the IAS1 sequence.

259 Prior to FAST, invasive procedures such as diagnostic peritoneal

260 t FAST-2 represents a new WH gene related to FAST-1, which functions to mediate TGF-beta signals in m

261 gram entitled Fast Analysis of SHAPE traces (FAST), which significantly reduces processing time.

262 ustrated and Allowed Structural Transitions (FAST) principle: the ease with which competing structura

263 e p15 fusion-associated small transmembrane (FAST) protein is a nonstructural viral protein that indu

264 Fusion-associated small transmembrane (FAST) proteins are a diverse family of nonstructural vir

265 Fusion-associated small transmembrane (FAST) proteins are viral nonstructural proteins that med

266 virus fusion-associated small transmembrane (FAST) proteins comprise a unique family of viral membran

267 ncode fusion-associated small transmembrane (FAST) proteins that induce syncytium formation.

268 with fusion-associated small transmembrane (FAST) proteins, which have previously been identified in

269 cused assessment with sonography for trauma (FAST) examination in children is unknown.

270 cused Assessment with Sonography for Trauma (FAST) has modest sensitivity for hemoperitoneum and IAI

271 used Assessment Using Sonography for Trauma (FAST) to discriminate between survivors and nonsurvivors

272 of focused abdominal sonography for trauma (FAST).

273 ocused assessment with sonography in trauma (FAST) has been extensively utilized and studied in blunt

274 ntimetabolites as Steroid-sparing Treatment (FAST) uveitis trial screened 265 adults with noninfectio

275 The For Angioedema Subcutaneous Treatment (FAST)-2, a phase III, double-blind, randomized, multicen

276 of an international phase 2 clinical trial (FAST II) evaluating telavancin for the treatment of comp

277 ly gathered data for all patients undergoing FAST for blunt trauma during a 30-month period.

278 inclusion criteria, of whom 85.0% underwent FAST and 86.1% abdominal CT; 159 (34.0%) had abdominal i

279 ts arrived in traumatic arrest and underwent FAST.

280 a closed-loop PET recycling process by using FAST-PETase and resynthesizing PET from the recovered mo

281 Trauma surgeons are routinely using FAST to evaluate patients with blunt trauma for hemoperi

282 AUC for RF versus FAST, FIB-4, and NFS for NASH + NAS >= 4 + >=F2 were (0.

283 d concentrations were both lower in CARB vs. FAST with negligible difference between CARB vs. NIACIN.

284 is then delivered to late endosomes, whereas FAST DiI, with two cis double bonds in each tail, and Di

285 ARE in a DNase I protection assay, in which FAST-2 binds the ARE around a motif (TGTGTATT) previousl

286 1 contains three FAST binding sites on which FAST/Smad transcriptional complexes can assemble; these

287 With FAST cytometry, laser-printing optics are used to excite

288 22 [95% CI, 1.02-4.85]) were associated with FAST >0.35.

289 We demonstrate that BF-1 associates with FAST-2.

290 ory activity by competitive association with FAST-2.

291 the FAST-2.ARE complex through binding with FAST-2.

292 o the nucleus where they form a complex with FAST-1 that requires these three components to activate

293 al responses to TGF-beta by interacting with FAST-2 or with other DNA binding proteins which function

294 Interference with FAST function abolishes intron 1 activity, and transcrip

295 the mouse which shares many properties with FAST-1.

296 Y-FAST distinguishes itself from other tagging systems bec

297 Y-FAST is as bright as common fluorescent proteins, exhibi

298 Y-FAST was engineered from the 14-kDa photoactive yellow p

299 ce-Activating and absorption-Shifting Tag (Y-FAST), a small monomeric protein tag, half as large as t

300 the Zometa-Femara Adjuvant Synergy Trial (Z-FAST) indicate that upfront zoledronic acid therapy prev