ライフサイエンスコーパス: reporter

1 simple fluorescent imaging for each lineage reporter.

2 rial Lux system is used as a gene expression reporter.

3 sing a novel cell surface Gaussia luciferase reporter.

4 g of genomic loci together with a cell cycle reporter.

5 belled detection antibody as a non-enzymatic reporter.

6 G stop codon located in a beta-galactosidase reporter.

7 codon-optimality or 5'UTR of the luciferase reporter.

8 (Jc1G), which encodes a secreted luciferase reporter.

9 eening assays with luciferase or fluorescent reporters.

10 mited by photon emission from single optical reporters.

11 thout the limitations associated with enzyme reporters.

12 were also recognized by KIR2DL2 and KIR2DL3 reporters.

13 ing of the apoptotic cells using quantum dot reporters.

14 w viral-based platforms with 2 specific gene reporters.

15 AT5 activation and inhibited STAT3-dependent reporter activation upon IL6-treatment.

16 de and cisplatin increased NFkappaB promoter reporter activity and etoposide induced nuclear transloc

17 LPS-induced NF-kappaB reporter activity and intracellular signaling by NF-kapp

18 OXA2 showed an impairment in transcriptional reporter activity by the mutant hFOXA2.

19 Nrf2 activators increased SREBP-1C promoter reporter activity in HepG2 cells.

20 RARE-EGFP reporter axolotls showed divergent reporter activity in limbs undergoing PD duplication ver

21 induction of GR target genes and GRE-driven reporter activity without disrupting dexamethasone-induc

22 , whereas overexpression increased PPARalpha reporter activity, suggesting ACOT1 regulates PPARalpha

23 ired for glial activation of transcriptional reporters after axonal injury.

24 odel of melanoma incorporating a fluorescent reporter allele (tdTomatoLSL).

25 Here we exploit a Prdm1.CreERT2-LacZ reporter allele for lineage tracing experiments.

26 Reporter analysis revealed that CircPVT1 decreased the c

27 Live translation reporter analysis reveals that de novo beta-actin hotspo

28 ate this system's utility in transcriptional reporter analysis, site-of-action experiments and exogen

29 es clones with an integrated fluorescent HIV reporter and Cas9 expression gene were generated.

30 omic annotation data and performing promoter-reporter and chromatin conformational capture (3C) studi

31 Luciferase reporter and electrophoretic-mobility shift assay for th

32 The expression of a protected fluorescent reporter and flux of a high-value metabolite are signifi

33 Promoter reporter and gel shift assays determined that the AirR r

34 Moreover, Yki activity reporters and epistasis tests showed that Yki does not m

35 In this study, we combine novel mouse reporters and single-cell RNA sequencing to reveal the h

36 ared with the (14)C-iodoantipyrine perfusion reporter, and the perfusion-modifying drugs nicotinamide

37 and transgenic mice expressing recombinases, reporters, and inducible transcriptional activators are

38 uction of KAR2, PDI1, and beta-galactosidase reporters, and survival of ER stress, but it had no effe

39 partner alters the efficiency with which the reporter approaches the electrode surface, thus causing

40 lycoFRET), where terbium-labeled fluorescent reporters are irreversibly attached to receptors by meta

41 ein immobilization process using fluorescent reporters as well as atomic force microscopy.

42 Using dual-luciferase reporter assay and Chromatin immunoprecipitation, we dem

43 g computational network analysis, an in vivo reporter assay and physiological validation experiments.

44 77; RNA immunoprecipitation and a luciferase reporter assay confirmed that ilp7 and ilp8 are direct t

45 Nevertheless, designing high-throughput reporter assay experiments such as massively parallel re

46 BPAF, Coum, 1-BP) of 16 compounds tested by reporter assay had estrogenic activity through mERbeta2.

47 oyed a Piwi-interacting RNA (piRNA)-targeted reporter assay in Drosophila ovary somatic sheet (OSS) c

48 purification (TRAP) and in vitro luciferase reporter assay indicate that mir-92a suppresses expressi

49 Dual luciferase reporter assay indicated that MdCCA1 but not MdCSP3 acti

50 RNA sequencing data and a uidA reporter assay indicated that the MybA protein functions

51 Dual-luciferase reporter assay revealed that bta-miR-23a directly target

52 Furthermore, Luciferase reporter assay reveals that Honokiol modestly increased

53 Pase activity of DHX9, and a transcriptional reporter assay suggests Nup98 supports DHX9-stimulated t

54 We developed a novel reporter assay that enabled identification of natural co

55 ombining computational modeling and the BiLC reporter assay, we identified several novel small-molecu

56 sing cAMP measurements and a transcriptional reporter assay, we observed that several constrained ago

57 Using a cell-based reporter assay, we screened C4a against a panel of both

58 etry, bioinformatics analysis and luciferase reporter assay, we showed that miR-K6-5p directly target

59 ncreased mRNA stability, as predicted by the reporter assay, while also markedly decreasing transcrip

60 sessed by RT-qPCR, ChIP assay and luciferase reporter assay.

61 tly targeted by miR-124-3p with a luciferase reporter assay.

62 assay experiments such as massively parallel reporter assays (MPRAs) and similar methods remains chal

63 Here, we used massively parallel reporter assays (MPRAs) involving 32,115 natural and syn

64 The results of chromosomally based reporter assays are also more reproducible and more stro

65 assessed using different T-cell factor (TCF) reporter assays as a readout for Wnt/beta-catenin-depend

66 Luciferase reporter assays confirmed the interaction between miR-12

67 Luciferase reporter assays confirmed the predicted interactions bet

68 Luciferase reporter assays demonstrated that high miR-375 expressio

69 Reporter assays demonstrated that rs9920291 shows alleli

70 pha-SYN expression; while exogenous promoter-reporter assays failed to reproduce the similar outcomes

71 Many studies using reporter assays have demonstrated that 3' untranslated r

72 Of note, reporter assays indicated that IRF5 re-expression inhibi

73 Chromatin immunoprecipitation and luciferase reporter assays revealed a direct binding of NANOG to a

74 Reporter assays revealed that promoters from different a

75 ciated loci, we performed massively parallel reporter assays to screen candidate functional variants

76 transcription and replication in luciferase reporter assays, a mutant that may act as a phosphomimet

77 tion with low micromolar IC50s in cell-based reporter assays, inhibit Gas6-inducible motility in Axl-

78 activity of 69 TE subfamilies by luciferase reporter assays, spanning all major TE classes, and show

79 Through quantitative proteomics and reporter assays, we found that the UBE3A(T485A) protein

80 Here, using luciferase-based reporter assays, we provide evidence that NRP1 regulates

81 Using GUS and GFP reporter assays, we reveal their distinct or overlapping

82 Due to intrinsic limitations of heterologous reporter assays, we sought to develop a gene editing app

83 eased translation efficiencies in luciferase reporter assays.

84 resulted in decreased luciferase activity in reporter assays.

85 ting the results of chromosomally integrated reporter assays.

86 eased transcriptional activity in luciferase reporter assays.

87 acterized at functional level using in vitro reporter assays.

88 s finding was confirmed using the luciferase reporter assays.

89 sing exogenous transfection-based luciferase reporter assays.

90 RARE-EGFP reporter axolotls showed divergent reporter activity in

91 Imaging of NFkappaB reporter before and after surgery showed a significant i

92 -associated viral vector driving the GCaMP6f reporter behind a synapsin promoter.

93 oluminescence resonance-energy-based Antares reporter called Antares2, which offers improved signal f

94 lar administration of lentiviral, luciferase reporter cassettes (biosensors); we present real-time an

95 Employing novel cytokine reporter cell assays, we verified that potency at TLR7 c

96 In this study, we present a novel reporter cell line capable of detecting live ebolaviruse

97 an HIV-1-inducible green fluorescent protein reporter cell line.

98 ically assessed using genetically engineered reporter cell lines that produce a fluorescent signal as

99 Here we describe a reporter cell-based assay to quantify inducible, replica

100 Utilizing a reporter cell-line it was confirmed that LCM activated T

101 r of ALK1 signaling in BMP9-challenged C2C12 reporter cells.

102 ort hairpin RNA (shRNA) targeted against the reporter coding region, we have characterized the dynami

103 a promoter-specific, fluorescent translation reporter confirmed clusters are the functional unit of g

104 Expression of the reporter construct EBS: beta-glucuronidase (GUS) was det

105 t a stable full-length enterovirus 71 (EV71) reporter construct was used to visualize real-time viral

106 EGFP-mini-nesprin-2G, a functional TAN line reporter construct, within the nuclear envelope.

107 ork independently over a targeted transgenic reporter construct.

108 s in RNAPII elongation in vivo on a splicing reporter construct.

109 ion in vitro by use of both the TCV gRNA and reporter constructs did not reveal any sequence-specific

110 induced from transgenic plants carrying GUS reporter constructs of these genes indicated that these

111 Some of the reporter constructs were preferentially expressed in the

112 used BAC recombineering to first create GFP reporter constructs, which were analysed for enhancer ac

113 que XDP SVA retrotransposon using luciferase reporter constructs.

114 This is followed by the translation of reporters containing 3' untranslated region of Mos or Cc

115 from 2000 to 2014 were accessed from the NIH RePORTER database.

116 paB and STAT3 transcription factor activated reporters during the earliest stages of development in l

117 ple knock-in of epitope tags and fluorescent reporters (e.g. Sox2-V5 and Sox2-mCherry); and (4) engin

118 Real-time imaging with reporter enzyme fluorescence (REF) that uses custom fluo

119 presence of an EDC leads to activation of a reporter enzyme, reported through a straightforward colo

120 t nature allows fusion with affinity tags or reporter enzymes as well as efficient maleimide chemistr

121 nges correlate both with mutants' growth and reporter expression defects.

122 veals rapid pulsatile level changes in Gata2 reporter expression in cells undergoing endothelial-to-h

123 rence fluorescent protein is nested within a reporter fluorescent protein to control for such artifac

124 ns in and around this core cluster express a reporter for corticotrophin-releasing hormone (Bar(CRH)

125 using a reporter virus expressing a surface reporter for gentle and efficient purification with long

126 we developed a specific translocation-based reporter for monitoring Fus3 activity in individual live

127 n enzymatically generated at biosensors as a reporter for the presence of nonelectroactive target mol

128 Here, through the use of a reporter for the signaling lipid S1P (sphingosine 1-phos

129 proliferating human cells, using fluorescent reporters for AMPK activity, Akt activity, and cytosolic

130 FP (large Stokes shift LSSmOrange) within a reporter FP (circularly permuted green FP).

131 In complementation assays, the reporter fragments are directly fused to the interacting

132 Fluorescent reporter fusions showed that SLI1 is confined to the mar

133 ibited serum response factor (SRF)-dependent reporter gene (SRE-LUC) activity and mRNA expression of

134 conditional hair cell-specific gene deletion/reporter gene activation in the inner ear.

135 e Gfi1(Cre) mice, both for gene deletion and reporter gene activation, these data are significant and

136 l MRTF/SRF inhibitor, markedly decreased SRF reporter gene activity and showed a greater inhibitory e

137 2 inhibitors on TGF-beta1-induced migration, reporter gene activity, and Smad activation.

138 es of CRM function undetected by traditional reporter gene analysis.

139 vity from the NtPDR1 promoter in situ with a reporter gene and found that, although NtPDR1 expression

140 Reporter gene and in silico transcription factor binding

141 We show that mRNA half-lives for a reporter gene are increased in both fast and slow Pol II

142 A fragment-based screening, reporter gene assay, and pharmacophore search were utili

143 d potent transcriptional activities in a VDR reporter gene assay, and significantly ameliorated cardi

144 Likewise, reporter gene assays demonstrated significantly lower GU

145 As shown in cell-based dual-luciferase reporter gene assays, functional interaction occurred be

146 Using multiple luciferase reporter gene assays, we could demonstrate that editing

147 47 like ETS transcription factor 5 (ELF5) in reporter gene assays.

148 lead risk variant region were analyzed with reporter gene assays.

149 wild-type AAV2 (wtAAV2) replication but also reporter gene expression from both single-stranded and d

150 d assays, including SMAD-mediated luciferase reporter gene expression, and differentiation of a multi

151 b promoter supports enhanced expression of a reporter gene in sphk2(MZ) embryos compared to wildtype

152 We succeeded in transferring a GFP reporter gene into adult hematopoietic stem cells in viv

153 hieve a 110-fold increase in expression of a reporter gene relative to non-replicating controls.

154 Fluorescence signal from the reporter gene was detected a few hours after transfectio

155 ly 14,000 E. coli strains, each expressing a reporter gene with a unique 5' architecture.

156 arted by the 5 UTR can be transferred onto a reporter gene, indicative that the 5 UTR can solely driv

157 ges were monitored using a novel fluorescent reporter gene, pMitoTimer, that allows assessment of mit

158 3 to induce expression of a STAT3-responsive reporter gene.

159 ced expression of an Asc promoter-luciferase reporter gene.

160 NIH-3T3 cells transfected with a beta-klotho reporter gene.

161 heterodimers-mediated transactivation of GUS reporter gene.

162 While employing reporter genes constructed with inducible promoters and

163 s (ULG8), which we have leveraged to express reporter genes in mature male and female gametocytes.

164 nalized virus remained capable of expressing reporter genes while viral replication was blocked.

165 hmark' vector titres are achieved with inert reporter genes.

166 We also show that reporters harboring stall sequences near the initiation

167 d-type skin grafted onto Fgfbp1 GFP-knock-in reporter hosts and bone marrow transplants from the GFP-

168 using the zeocin resistance gene sh-ble as a reporter in monocistronic and dicistronic constructs, an

169 used it to drive expression of a transgenic reporter in Sertoli cells.

170 e mouse in vivo can also regulate its 3' UTR reporter in the liver of another mouse through serum exo

171 ables accurate quantification of fluorescent reporters in complex human iPSC-derived retinal organoid

172 long with unique fluorescent protein lineage reporters in the same mouse.

173 ntification of glycans through comparison of reporter ion intensities.

174 hick silica shell wherein the resonant Raman reporter is embedded.

175 , in applications where a small fluorescence reporter is required or desirable, the choice of fluorop

176 We now show using fluorescent reporter knockin lines that Fgfr1 is expressed in all ce

177 Kinase translocation reporters (KTRs) are genetically encoded fluorescent act

178 We have developed kinase translocation reporters (KTRs), which enable multiplexed measurements

179 H target tissues using a novel TH-responsive reporter line and found that both alpha- and beta-cells

180 We now report a new Hmox1 reporter line that makes it possible to obtain this info

181 ther a Cre-dependent tdTomato or Brainbow2.1 reporter line.

182 Here, we combine dopamine receptor reporter lines, anatomical tracing techniques, and elect

183 o mechanistic analysis or rely on artificial reporter loci.

184 We generate Rosa26-mT/sr39tk PET reporter mice and induce sr39tk expression in platelets,

185 Foxp3-mRFP/cd69(+/-) or Foxp3-mRFP/cd69(-/-) reporter mice and short hairpin RNA (shRNA)-mediated sil

186 Double IL-10(eGFP) Foxp3(mRFP) reporter mice and transgenic mice with impairment in IL-

187 These data support the use of VEGFR3 reporter mice as a 'MetAlert' discovery platform for dri

188 y as well as the use of Cldn14-lacZ knock-in reporter mice confirmed increased Cldn14 expression and

189 Analysis with Treg fate-mapping reporter mice further demonstrates that IL-27 signaling

190 e, transcriptome analysis using IL-17A(hCD2) reporter mice revealed a similar gene expression profile

191 IL-10 green fluorescent protein reporter mice revealed that regulatory T (Treg) cells we

192 Studies with IL-4-IRES-eGFP (4get) reporter mice showed eosinophils were the main IL-4-prod

193 nts in the epidermis of the hind paws of the reporter mice showed that EGTA and MDL28170 diminished c

194 In transgenic reporter mice with normal angiopoietin-Tie2 signaling, m

195 n sensitization were analyzed using cytokine reporter mice, an adoptive cell transfer model, and gene

196 ated recombination was assessed by using Cre-reporter mice, polymerase chain reaction of genomic DNA,

197 al multiphoton microscopy of DC(GFP)/MC(RFP) reporter mice, we herein provide in vivo evidence that m

198 Using bigenic Gli1-CreER(t2); R26tdTomato reporter mice, we observed increased distance between Gl

199 -type C57BL/6 mice as well as from Wnt1-Cre2 reporter mice.

200 Manipulation of the UCE, in a reporter minigene or via random mutations in the genomic

201 sts and bone marrow transplants from the GFP-reporter model into wild-type hosts revealed that circul

202 In a new Hmox1 reporter model we provide high-fidelity, single-cell res

203 eproducible SERS spectra were obtained using reporter-modified gold nanoparticles (AuNPs).

204 ninvasive imaging of animal subjects bearing reporter-modified intracranial xenografts, we quantitati

205 r electrochemical sensors consist of a redox-reporter-modified protein (the "receptor") site-specific

206 that changing the 3'UTR of a miRNA-targeted reporter modulates translational repression by affecting

207 n of the dimerized origami to act as a Raman reporter molecule.

208 ry detection strand coupled with a sensitive reporter molecule.

209 r chemical structure allows the insertion of reporter molecules and surface-binding agents in specifi

210 trategy, we expressed multiple complementary reporter molecules from the murine Hmox1 locus, includin

211 DMA allows for the detection of redox-active reporter molecules irrespective of their electrochemical

212 e of DCs in renal inflammation using a CD11c reporter mouse line and two mouse lines with DC-specific

213 Immunohistochemical staining in an aromatase reporter mouse revealed that many neurons in laminae I a

214 The authors used the PW1(nLacZ+/-) reporter mouse to identify, track, isolate, and characte

215 havior of dHSCs in situ, a Gprc5c-controlled reporter mouse was established.

216 ng cytosolic Ca(2+), and a transgenic Ca(2+) reporter mouse with Salsa6f targeted to the Rosa26 locus

217 artificial chromosome (BAC)-based lymphatic reporter mouse, where EGFP is expressed under the regula

218 of which selects for translation of viral or reporter mRNAs with 5' untranslated regions that contain

219 dividual isolated cells, we measured knockin reporters, mRNAs, signaling (phosphorylation of extracel

220 ate that endogenous Nur77 is a more specific reporter of Ag-specific signaling events than the common

221 ontrast with previous reports of S100A4 as a reporter of EMT, we discovered that S100A4 is an upstrea

222 nous Nur77 protein expression can serve as a reporter of TCR and BCR specific signaling in human PBMC

223 e used time-lapse microscopy and fluorescent reporters of DNA replication and chromosome positioning

224 ave emerged as a powerful class of molecular reporters of location and environment.

225 rker genes as well as surprisingly sensitive reporters of off-target transgene expression.

226 Here, using two independent optical reporters of PKA activity in acute mouse hippocampus sli

227 r rDNA cluster unambiguously and use them as reporters of rDNA cluster-specific expression.

228 60,000 shRNAs using a cell line with a MeCP2 reporter on the Xi and found 30 genes clustered in seven

229 f aggregated silver nanoparticles with Raman reporters on them was synthesized and functionalized to

230 oduce azide, one of the most useful chemical reporters, onto a broad range of bioactive azaheterocycl

231 d "others" (not meeting criteria for perfect reporter or overreporter).

232 se models used in research involve knock-in (reporters or recombinases) or gene replacement (e.g., co

233 studying real-time signatures of fluorescent reporters placed on RNAP and DNA in the presence of liga

234 ronJet hereafter) device was used to deliver reporter plasmids (pCMVbeta and pEGFP-N1) into viable ex

235 and developmentally differentiated NKX2-1GFP reporter pluripotent stem cells (PSCs) in vitro to gener

236 Detoxification of aggregated reporter polypeptides as well as misfolded endogenous pr

237 ts and subsequently to a single stranded DNA reporter probe bearing a HRP molecule, followed by subst

238 med BC2T) and BC2 nanobody-dye conjugates or reporter protein fusions are evaluated in ELISA, flow cy

239 s results in the in-frame translation of the reporter protein hence the sparse neuronal labeling.

240 cell variations in the abundance of mRNA and reporter protein in yeast.

241 ing a full-length, approximately 45-kDa K15P reporter protein is expressed as an approximately 23- to

242 aration and purification of chemical dye- or reporter protein-antibody conjugates is often complicate

243 e that enables bioelectronic measurements of reporter proteins in living cells as an alternative to t

244 Moreover, Gata2 reporter pulsatile expression is dramatically altered in

245 , we report development of a novel lymphatic reporter rat using the mouse Prox1-EGFP BAC.

246 el in which the positive and negative energy reporters regulate AGPase catalytic activity via intra-

247 s by >97%, but it did not reduce the KIR2DS2 reporter responses, indicating a beta2-microglobulin-ind

248 The MBSV6 reporter revealed that, in contrast to previous findings

249 artments of surgery were collected using NIH RePORTER, Scopus, and departmental websites.

250 Patients were classified as "perfect reporters" (self-report agreed with MEMS), "overreporter

251 approaches using subcellularly targeted FRET reporter sensors have helped define more compartmentaliz

252 e bacterial cytoplasm of an Escherichia coli reporter strain.

253 Using region-specific mouse reporter strains, we performed an RNA-seq screen, identi

254 eage tracing by using Cdh5cre(ERt2)/Rosa-YFP reporter strategy demonstrated that the CD31-/loVEGFR2lo

255 Expression of the OsK5.2 gene (GUS reporter strategy) was observed in the whole stomatal co

256 In vivo reporter studies demonstrated that the Mgp promoter is h

257 -binding motif that was supported in vivo by reporter studies, and in vitro by run-off transcription

258 cells and promoter activity using luciferase reporter studies.

259 Here, we utilized a loss-of-function HR-reporter substrate to simultaneously monitor HR-mediated

260 ty, prevents the translation of Mos or Ccnb1 reporters, suggesting that MPF is required for their tra

261 OSTs in vivo using a transgenic glycoprotein reporter system and performed glycoproteomics on endogen

262 Here we develop a 4-colour fluorescence reporter system at the single-virus level, combined with

263 A universal reporter system for in-cell protein kinase profiling wil

264 lfides were investigated using a fluorescent reporter system in order to optimize linker stability fo

265 A newly-developed modular reporter system proved possible to demonstrate that PpMm

266 We developed a cell-based reporter system to quantitate pathogen-specific antibody

267 RNAs, and a newly developed luciferase-based reporter system to quantitatively determine the importan

268 ed on this data, using a newly developed gfp reporter system we validate an Hfq-dependent mRNA repres

269 Using a transcription-normalized reporter system, we discovered that stop codon readthrou

270 transformed cells programed with fluorescent reporter systems and by quantitative cell imaging, the c

271 us genes cannot be faithfully represented by reporter systems in which, at least in metazoans, the ob

272 logically active Cre recombinase into a loxP-reporter T cell line.

273 this observation, we biochemically isolated reporter-tagged Mbp mRNA granules from primary cultured

274 anscription factor activated luciferase/eGFP reporter (TFAR) cassettes to neonatal mice enabling long

275 lia, resulting in changes in transcriptional reporters that are dependent on Drosophila AP-1 (dAP-1)

276 ton microscopy with two different activation reporters, the FRET-based calcium biosensor Twitch1 and

277 We describe a cellular reporter to directly monitor the phenotypic switch in dr

278 eq, which uses a Cre recombinase interaction reporter to intracellularly fuse the coding sequences of

279 re, we use a DNA-based, fluorescent chloride reporter to measure lysosomal chloride in Caenorhabditis

280 es, we generated a novel class of FRET-based reporter to monitor conformational differences correspon

281 We have used these reporters to measure differences in BER capacity across

282 ver, we demonstrate the suitability of these reporters to measure differences in DRC in multiple path

283 re, we use behavioral assays and fluorescent reporters to show that axonal fusion enables full recove

284 As were generated from a 35S promoter::GU-US reporter transgene targeted by CRISPR/Cas9.

285 , termed Specific High-Sensitivity Enzymatic Reporter UnLOCKing (SHERLOCK), to detect specific strain

286 he translocation efficiency of the resulting reporter variants.

287 f human embryonic kidney 293 cells with this reporter vector increased luciferase activity upon stimu

288 These results demonstrate that our TREM2 reporter vector is a novel tool for monitoring the TREM2

289 d enrichment of HIV-1 infected cells using a reporter virus expressing a surface reporter for gentle

290 t and a ZIKV C-prM-E cell line that produces reporter virus particles upon transfection with a GFP re

291 An inducible-AMS reporter was created for functional rescue, protein expr

292 l integration, the hTERT, but not the mTert, reporter was stringently repressed in telomerase-negativ

293 l lysate and purified target mRNA fused to a reporter was used to identify active zwitterions.

294 e efficacy of the developed, fully synthetic reporters was demonstrated by the identification of nove

295 Using a plasmid-based reporter we found that LuxR can mediate repression of ai

296 Using Grb2 as a phosphorylation reporter, we further monitored LAT phosphorylation by TC

297 Using a photoconvertible patched2 reporter, we resolve active Hh/Smo output to a narrow di

298 selection of promoter regions for transgenic reporters, we assembled and annotated the M. lignano gen

299 amethasone-mediated transactivation of a GRE reporter while still maintaining its actin-binding activ

300 se line and two mouse lines with DC-specific reporters, Zbtb46-GFP and Snx22-GFP.