ライフサイエンスコーパス: tracing

1 engaged in two different tasks (copying and tracing).

2 ) were examined by means of carbocyanine dye tracing.

3 on of conventional Cre-loxP-mediated lineage tracing.

4 tely 10 nm, as measured by using PET imaging tracing.

5 Stem Cell tenth anniversary theme of lineage tracing.

6 somes from neurons infected after retrograde tracing.

7 tients, 991 (17%) were randomly selected for tracing.

8 al areas, as determined by anterograde tract tracing.

9 RT2 (Alpi(CreER)) knockin allele for lineage tracing.

10 for RGC-targeting and with Cy5.5 for unimNP-tracing.

11 l aspect of the prostatic urethra by lineage tracing.

12 onary angiography and evaluated all pressure tracings.

13 One year after selection for tracing, 13.3% (95% confidence interval [CI], 11.1%-15.3

14 c decayed with a half-life of 7.0 days after tracing (95% CI, 2.6 %-12.9%).

15 this in chains of up to 42 trapped ions, by tracing a single phonon excitation through interferometr

16 power was calculated for all patients by ray tracing, aiming for postoperative emmetropia.

17 Recent technological advances in lineage tracing allow us for the first time to study these proce

18 ral labeling and manipulation, and classical tracing allowed us to identify second-order sensorimotor

19 glucose, (13)C lactate, and (13)C fatty acid tracing analyses to show that hearts in late pregnant mi

20 Cystometrogram study and tracing analysis of voiding behavior revealed that the k

21 Cadm1 protected mice from obesity, and tract-tracing analysis revealed Cadm1-positive innervation of

22 Lineage-tracing analysis revealed that descendants of Sfrp5-expr

23 Lineage tracing analysis revealed the conversion of beta-cells l

24 By lineage tracing analysis, we also found that collagen-expressing

25 tamoxifen-inducible Cre for cellular lineage-tracing analysis.

26 essment philology to explore this notion, by tracing and assessing the quantitative flows of energy e

27 t generation sequencing for antibody lineage tracing and B cell fate mapping.

28 igin(s) of infarct fibroblasts using lineage tracing and bone marrow transplants and a robust marker

29 In dual retrograde viral tracing and c-Fos immunostaining experiments, we found t

30 vo over an extended timespan, combining cell tracing and cell fate marker expression over time.

31 e dLGN, Pv, and claustrum, using anterograde tracing and electron microscopy.

32 aptic neuronal targets, thus allowing axonal tracing and functional manipulations of the latter input

33 Here we show through lineage tracing and genetic ablation that BMI1(+) CSCs mediate i

34 By combining isotope-tracing and genetic experiments, we have demonstrated th

35 Lineage tracing and immunohistochemical analyses revealed clonal

36 region and depict rabies-based transsynaptic tracing and LSFM as efficient tools for comprehensive as

37 hnique for anterograde transsynaptic circuit tracing and manipulation.

38 Detailed anatomical tracing and mapping of the viscerotopic organization of

39 Here we use cell lineage tracing and multiple in vivo approaches to study the rol

40 In zebrafish, previous lineage-tracing and mutant analyses suggested that SHF ventricul

41 Using genetic lineage-tracing and neural crest-deficient mutants in zebrafish,

42 We used cell-type-specific anterograde tracing and optogenetic methods to selectively label and

43 By combining anatomical tracing and optogenetic/pharmacological manipulations, w

44 marker expression patterns, genetic lineage tracing and parabiosis.

45 Lineage tracing and quantitative clonal analysis reveal that, fo

46 Here, we employed in vivo lineage tracing and real-time gene expression transgenic reporti

47 Using genetic lineage-tracing and scanning-block face electron microscopy, we

48 The tracing and screening of contacts of known patients with

49 ve outbreak investigation, including contact tracing and stringent surveillance.

50 ction between the target IOL measured by ray tracing and that calculated with third-generation formul

51 he expected residual refraction based on ray tracing and that predicted with the third-generation for

52 of melanoma, we combined single-cell lineage-tracing and transcriptomics approaches with time-lapse i

53 Using in vivo lineage tracing and triple negative breast cancer (TNBC) patient

54 sistent with egocentric neglect in one task (tracing), and allocentric neglect in another task (copyi

55 combines immunohistochemistry, neural tract tracing, and electron microscopy to investigate the orig

56 single cell transplantation, in vivo lineage tracing, and HSC-specific pulse-chase labeling have prov

57 on that included patient interviews, contact tracing, and serum testing, as well as environmental and

58 We employ genetics, cell lineage tracing, and single molecule imaging to show that mutati

59 active tuberculosis (case finding), contact tracing, and treatment completion.

60 hors combined in vivo recordings, retrograde tracings, and reconstructions of PTs in rat somatosensor

61 m was evaluated via comparison to the manual tracings, and the automatically located landmarks were u

62 ng, Gli1 expression was examined via lineage tracing approaches and the effect of Smo deletion was ex

63 using cellular markers, but recently lineage tracing approaches have proven that cells are highly pla

64 However, current lineage-tracing approaches scale poorly to whole, complex organi

65 We used genetic modifications and (13)C tracing approaches to define glutamine metabolism in the

66 Using genetic lineage-tracing approaches, we show that in the postnatal murine

67 Using SRS-based isotope tracing assay to quantitatively track lipid synthesis an

68 It provides information that is useful for tracing axonal bundles and inferring brain connectivity.

69 ceptive systems may share a common ancestry, tracing back to a progenitor that lived more than 500 mi

70 tDNA lineage ancestries of the NPR Scythians tracing back to hunter-gatherer and nomadic populations

71 imulate a set of disease outbreak scenarios, tracing billions of stochastic trajectories of fungal sp

72 dom sample of LTFU patients was selected for tracing by peer health workers.

73 Lineage tracing by using Cdh5cre(ERt2)/Rosa-YFP reporter strateg

74 For redox reactions, deuterium tracing can provide additional information.

75 resolve complex mixtures of cancer cells by tracing cell lineages and discovering cryptic genetic va

76 anging applications, such as in deep lineage tracing, cellular barcoding, molecular recording, dissec

77 Clonal genetic tracing combined with immunohistochemistry revealed that

78 Retrograde tracing combined with single-cell mRNA amplification ind

79 Using in vivo and in vitro cell fate tracing concomitant with specific cell ablation and embr

80 We used lineage tracing, conditional deletion, mosaic analysis and ligan

81 Lineage tracing confirmed that LDB1-depleted, insulin-negative b

82 Genetic lineage tracing confirms the presence of the Tbx6(+) NMP cell st

83 testinal epithelium, and a year-long lineage-tracing course revealed that genetic blockade of LGR5 in

84 Comparing macaque MSNs with tract-tracing data confirmed that morphometric similarity was

85 Lineage tracing distinguished macrophages from classical DCs, ne

86 elium isotopes provide an important tool for tracing early-Earth, primordial reservoirs that have sur

87 control of Cre-loxP recombination in lineage tracing, effectively circumventing potential uncertainty

88 This study provides direct lineage tracing evidence that a cardiomyoblast population contri

89 les from mice with Wilson's disease and also tracing exogenously added copper in serum.

90 The cell-tracing experiment shows that cells in the 1.0 x 10(7) g

91 A cell tracing experiment was included to observe the preservat

92 knock-in Cre drivers used to perform lineage tracing experiments are often dynamically, temporally, a

93 ation process was validated by using lineage-tracing experiments based on Sox18Cre(ERt2)/Rosa-YFP mic

94 However, lineage-tracing experiments demonstrate that cells from the earl

95 Retrograde fluorogold tracing experiments demonstrate that Neurod6(+) midbrain

96 Recently, genetic lineage tracing experiments have revealed chondrocyte progenitor

97 Finally, retrograde and anterograde tracing experiments identified the basilar pontine nucle

98 Here, by lineage-tracing experiments in fetal or postnatal mice, we disco

99 Lineage tracing experiments in Foxc1 mutant mouse cerebella indi

100 By targeted metabolomics and isotope tracing experiments in loss- and gain-of-function cell a

101 In vivo lineage-tracing experiments in molars showed the contribution of

102 Lineage-tracing experiments indicated that the majority of COL1-

103 Lineage tracing experiments of the gastric corpus in mice have n

104 Anterograde and retrograde tracing experiments revealed a topographically organized

105 Lineage tracing experiments revealed accumulation of ex-Foxp3(+)

106 Lineage-tracing experiments revealed that PW1(+) cells different

107 Lineage-tracing experiments revealed that the cells that accumul

108 Lineage tracing experiments show that Bglap-expressing cells in

109 Furthermore, our long-term lineage tracing experiments show that cerebellar Olig gene-expre

110 Lineage tracing experiments show that GATA/CD24hi cells have the

111 However, lineage-tracing experiments using an inducible Tbx18-CreERT2 lin

112 rts expertly collated from published pathway tracing experiments, and 5,394 connections of a possible

113 Through metabolomics and direct isotope tracing experiments, we find a number of metabolic abnor

114 dm1.CreERT2-LacZ reporter allele for lineage tracing experiments.

115 components by means of in vivo and in vitro tracing experiments.

116 immunohistochemistry and conventional tract tracing facilitated the definition of two separate but a

117 Here we use a combination of retrograde tracing, fast-scan cyclic voltammetry, electrophysiology

118 on of immunofluorescence and transganglionic tracing following injections of CTB in the tracheosyring

119 first direct evidence using genetic lineage tracing for two basic assumptions in Schwann cell biolog

120 ng, interpreting, and archiving the pressure tracings for daily practice and for the purpose of clini

121 pidermal proliferation with expanded lineage tracing from epidermal stem cells positive for Lgr6 expr

122 rajectories of these pathways via retrograde tracing from the high cervical spinal cord.

123 Retrograde tracing from the OB or posterior piriform cortex (PPC) s

124 ne search was used to identify or locate ECG tracings from patients with LPF-VTs.

125 n-deleted rabies virus-mediated monosynaptic tracing has become a standard method for neuronal circui

126 In the lung, lineage tracing has been used to identify distinct epithelial st

127 Rabies virus-based monosynaptic tracing has been used to identify neuronal circuits in v

128 Child contact tracing has been widely recommended but poorly implement

129 Rabies virus-based retrograde tracing has developed into a powerful approach for visua

130 Recent advances in connectomics and rabies tracing have yielded much higher estimates of retinogeni

131 The effect of tracing human immunodeficiency virus (HIV)-infected pati

132 Lineage tracing identified intrinsic recruitment of Scx-lineage

133 Anterograde and retrograde tracing identified the cortical and subcortical structur

134 Here, we used neuroanatomical tracing, immunofluorescence, and confocal imaging to dem

135 ations including cell tracking, neural tract tracing, immunoPET, and functional beta-cell mass quanti

136 tissue staining and clearing, or retrograde tracing in a MET(EGFP) transgenic mouse, we identify thr

137 Lineage tracing in Helicobacter-infected Slfn4 reporter mice rev

138 Using lineage tracing in Lgr5-EGFP-CreERT2/Rosa26-Tomato and Lgr6-EGFP

139 Genetic lineage tracing in mice indicates that gastrin expression is tur

140 By lineage tracing in mice, we have shown recently that club cells

141 Furthermore, lineage tracing in postnatal and adult glands provides the first

142 tem cell-derived clones using sparse lineage tracing in the regenerating mouse olfactory epithelium.

143 l for interpreting monosynaptic rabies-based tracing in the sensory system.

144 Here, we show using genetic fate tracing in two murine models of BMF that Gli1(+) mesench

145 symptom monitoring, implemented via contact tracing, in controlling epidemics using an agent-based b

146 live, personally contacted, and out of care, tracing increased the absolute probability of return at

147 Genetic lineage tracing indicated that stromal cells blocking the ureter

148 Monosynaptic transsynaptic rabies tracing indicated the pathway contacts multiple cell typ

149 creatic ductal adenocarcinoma, where lineage tracing indicates that Cytokeratin-Synaptophysin dual po

150 Tracing interventions increase reengagement, but develop

151 (15)N isotope tracing is an effective and direct approach to investiga

152 Quantitative ray tracing is applied to optimize the linearity and minimiz

153 epartment of Chemistry at Purdue University, tracing its history and mode of operation.

154 comprehensive infrared (IR)-fingerprints for tracing kerogen evolution.

155 isadvantages of mCT scans for the purpose of tracing large neuron profiles.

156 and PDAC expressed the duct-specific lineage tracing marker yellow fluorescent protein.

157 tal corneal refractive power (CATCRP), a ray-tracing method, with that derived from simulated keratom

158 we present CRISPR-UMI, a single-cell lineage-tracing methodology for pooled screening to account for

159 onventional anterograde and retrograde tract-tracing methods to better define the relationship betwee

160 In this study, we use genetic lineage-tracing models and adoptive transfer protocols to addres

161 -cell-specific and pericyte-specific lineage-tracing models to trace the fate of perivascular cells i

162 re MHCII(lo) subset as identified by lineage-tracing models.

163 planning, newborn registration and defaulter tracing, monitoring of routine immunization activities,

164 Using lineage tracing, murine models of heart calcification and in viv

165 Most current approaches to imaging and tracing neuronal 3D morphology are data intensive.

166 d single-cell sequencing and genetic lineage tracing of c-kit(+) cells to determine whether various p

167 with further development SYNseq will enable tracing of complex circuits at high speed and low cost.

168 iginal source of contamination, allowing the tracing of contamination-sourced Hg throughout the study

169 neuroscience, we found that ExM enabled the tracing of fine processes of radial glia, which are not

170 Here we show that lineage tracing of Gdf5-expressing joint interzone cells identif

171 hemogenetic manipulations and trans-synaptic tracing of genetically identified dorsal horn and RVM ne

172 se flux was measured by using stable isotope tracing of glycolytic and tricyclic acid intermediary me

173 We conducted anatomical tracing of mPFC projections and optogenetic interrogatio

174 abies viruses (PRVs) that enabled retrograde tracing of neural inputs that terminate on Cre-expressin

175 Epidemiological contact tracing of patients and Bayesian phylogenetic analysis o

176 stration to healthy rodents not only allowed tracing of primary visual pathways, but also enhanced th

177 ined clonogenic growth in vitro, and lineage-tracing of Prox1(+) cells revealed long-lived clones dur

178 limitation of rabies virus-based retrograde tracing of sensory neurons in adult mice, and may help t

179 Here, we performed clonal multicolor lineage tracing of skeletal muscle stem cells (MuSCs) to address

180 where the excellent z resolution can help in tracing of small neuronal processes and accelerate the t

181 the most widely used technology for in vivo tracing of stem or progenitor cell lineages.

182 Consequently, tracing of the delta(13)C variations in grassland ecosys

183 using synthetic chemistry enables the direct tracing of the drug molecule without substantially alter

184 gation in 3D cardiac tissues, enable in situ tracing of the evolving topology of 3D conducting pathwa

185 lineage-labeling approach gives more precise tracing of the lineage contribution of mural cells in vi

186 igh content of alpha-helices in Tra1 enabled tracing of the majority of its main chain.

187 al leukemia clones precludes high-resolution tracing of their clonal dynamics.

188 Tracing of Troy(+) cells during nephrogenesis demonstrat

189 Sequence Repeat) marker to a discriminating tracing of two different species of bioinoculants in soi

190 important information allows for analytical tracing of variations of scaling relationships and a phy

191 The effect of tracing on rate of return to clinic decayed with a half-

192 lected for tracing to identify the effect of tracing on reengagement.

193 METHODS AND Using genetic lineage tracing or bone marrow transplant, we found no evidence

194 iating ART, weighted estimates incorporating tracing outcomes found that 2 years after ART, 69% were

195 ration with Ebola testing as well as contact tracing, quarantining, and treatment.

196 gamma-tracing rates were shown to be 100%, 88.9%, 55.6%, and 5

197 we investigate homo-oligomeric interfaces by tracing residue coevolution via the global statistical d

198 Tract-tracing retrograde labeling suggests that telencephalic

199 val [CI], 11.1%-15.3%) of those selected for tracing returned compared with 10.0% (95% CI, 9.1%-10.8%

200 Retrograde tracing revealed that somata associated with different a

201 In vivo lineage tracing revealed that the gene transfer of SeV-GMT was m

202 Genetic in vivo lineage tracing revealed that the Krt15 promoter marks a long-li

203 Surprisingly, virus-based anatomical tracing revealed that very young, one-week-old, new gran

204 tal data are in good agreement with particle tracing simulations suggesting post-acceleration of prot

205 Ray tracing simulations support the measurement results.

206 We used genetic lineage tracing, single-cell RNA sequencing, and organoid cultur

207 Tracing stable isotopes, such as (13)C using various mas

208 edifferentiating cells using several lineage-tracing strains and single-cell mRNA-seq, and we show th

209 Using 2 independent lineage-tracing strategies in murine models, we show that cells

210 We use multiple models and lineage tracing strategies to show that this squamous-columnar j

211 A dual-virus tracing strategy combining retroviral birthdating with r

212 , we show, using a virus-based transsynaptic tracing strategy from the diaphragm muscle in the mouse,

213 Here, we have employed a lineage-tracing strategy that uses a tamoxifen-dependent, promot

214 Employing a p63(CreERT2)-based lineage-tracing strategy, we identified a unipotent fate for pro

215 Moreover, using a lineage tracing strategy, we provide evidence that high MAPK act

216 can complicate the interpretation of lineage-tracing studies and has caused controversy in many previ

217 using resting state functional connectivity, tracing studies conducted in non-human primates dissocia

218 In addition, lineage-tracing studies demonstrated that B cells do not act as

219 Tract tracing studies demonstrated that Ovvm is a major target

220 Lineage tracing studies demonstrated that the original Gli1+ cel

221 Recent lineage-tracing studies have shown that mature hepatocytes (MHs)

222 sclerosis is a hallmark of FSGS, and genetic tracing studies have shown that parietal epithelial cell

223 enables accurate interpretation of deuterium tracing studies of redox cofactor and fatty acid metabol

224 he present study, retrograde and anterograde tracing studies revealed a previously undescribed projec

225 Although Fos and transneuronal tracing studies strongly suggest that integration of MGE

226 ectome derived from complete neuroanatomical tracing studies, a recent study in PLOS Biology shows th

227 Metabolomics, including metabolic tracing studies, are an integral part of elucidating the

228 of ammonia, significantly limiting metabolic tracing studies.

229 N-ammonia in a cell lysate for (15)N-isotope tracing studies.

230 Here we describe a new genetic lineage tracing system that incorporates the Dre-rox recombinati

231 We used an anterograde tracing technique developed in our laboratory to selecti

232 We extend the use of a novel tracing technique to quantify the bioavailability of zin

233 re we use various retrograde and anterograde tracing techniques both in vivo and in vitro, intracellu

234 er, recent investigations using cell lineage tracing techniques have demonstrated that many, perhaps

235 A, and RMTg using retrograde and anterograde tracing techniques in the rat.

236 laustrum, we used anterograde and retrograde tracing techniques to elucidate the connectivity of DEn.

237 dopamine receptor reporter lines, anatomical tracing techniques, and electrophysiology to show that D

238 Recent studies using genetic lineage tracing technology have implicated diverse organ-residen

239 Using lineage tracing, temporal single-cell analyses, and chromatin la

240 g their own, that suggested based on lineage tracing that mural cells are adipogenic, contrasting wit

241 Strategic network tracing that starts with recently infected persons could

242 Here, we demonstrate by cell lineage tracing that the gills of a cartilaginous fish, the litt

243 erize neurons expressing the Gpr151 gene, by tracing the afferent connectivity of this diencephalic c

244 Tracing the differentiation of DC from the bone marrow t

245 By tracing the distribution of epialleles throughout the tu

246 system has emerged as a potential proxy for tracing the Earth's atmospheric evolution based on a red

247 By tracing the emergence of a language-cognition link in in

248 ed iPSC-CMs after initial differentiation by tracing the engraftment ratio (ER) using in vivo biolumi

249 Tracing the evolution of enzyme activity and stability f

250 s are introduced here as a powerful tool for tracing the fate of Cd in agricultural soils, and potent

251 Furthermore, by tracing the full lithiation procedure, the evolution of

252 dicated that these matrices could be used in tracing the geographical origin of animal produce and ti

253 Tracing the innervation, we found two previously undescr

254 viruses have emerged as a powerful tool for tracing the inputs to genetically defined populations of

255 re, developing a spatially explicit approach tracing the location of water use and water scarcity rel

256 Technological advances in mapping and tracing the oxidized forms of 5mC allow further dissecti

257 lecular epidemiological tool, especially for tracing the source of contamination in an event of a B.

258 In a genetic lineage tracing the WT1(CreERT2+/-)Rosa(tdT+/-) mouse model subj

259 cognizing Dhb-modified proteins and allowing tracing them as they form.

260 volution has long fascinated biologists, but tracing this complex of behavioural repertoires is chall

261 st statistical analyses with in vivo lineage tracing to define a detailed map of the postnatal olfact

262 ll proliferation assays, and genetic lineage tracing to define the lineage relations and restrictions

263 et al. (2017) use elegant MADM-based lineage tracing to demonstrate cell-intrinsic and global functio

264 In this study, we used multicolor lineage tracing to demonstrate that polyclonal seeding by cell c

265 and Kohler et al. (2017) use in vivo lineage tracing to demonstrate that these two possibilities may

266 resent study, we used fluorescent retrograde tracing to determine the olivary inputs to the ZII+ and

267 We next employed inducible lineage tracing to fate map, through Cre recombinase-mediated fl

268 ich LTFU patients were randomly selected for tracing to identify the effect of tracing on reengagemen

269 bies virus -mediated monosynaptic retrograde tracing to label the inputs and adeno-associated virus t

270 targeted single-cell-initiated transsynaptic tracing to label the retinal ganglion cells that provide

271 Here we use genetic lineage tracing to mark the Nppa(+) or Hey2(+) cardiomyocytes as

272 nsional reconstruction was combined with ray tracing to simulate a daily time course of radiation pro

273 on their employment of a battery of lineage-tracing tools to address the developmental origins of fi

274 Tracing transcriptional differences with a high spatial

275 Lineage-tracing, transcriptome, and chromatin analyses showed th

276 We assessed the effect of selection for tracing using Kaplan-Meier estimates of reengagement amo

277 We performed conditional anterograde tracing using mice that express Cre recombinase only in

278 Lineage tracing using Rosa-td tomato (Col2-Cre-ERT2) mice treate

279 Increasing the feasibility of child-contact tracing using these approaches should be encouraged to d

280 ing intervals derived from the cuff pressure tracings using three different pulse landmarks.

281 Here we test this hypothesis by tracing variations in the abundance of fossil charcoal a

282 We used anterograde tracing, viral-mediated gene silencing, functional disco

283 Dual injection of GFP and mCherry tracing viruses simultaneously illuminates nigrostriatal

284 -mediated putative retrograde trans-synaptic tracing was used to identify and compare presynaptic inp

285 on with invasive hemodynamic aortic pressure tracings was performed.

286 Using additional prospective lineage tracing, we demonstrate that while SHF ventricular proge

287 Through in vivo lineage tracing, we demonstrated the power of this approach by s

288 Using cell lineage tracing, we further demonstrate that trunk neural crest

289 Using viral-mediated circuit tracing, we have identified the local circuits of L4B ne

290 Using rabies virus monosynaptic tracing, we mapped cocaine-induced global changes in inp

291 Using anterograde viral tracing, we show that innervation of cerebellum by rubro

292 Using sonic hedgehog lineage tracing, we show that the third and fourth ventricle E2

293 Using genetic lineage tracing, we systematically investigated the role of cell

294 Pressure tracings were analyzed offline over 8 to 10 beat interva

295 Cre-lox-mediated tracing, which included following Brainbow clones, furth

296 male mice, using pathway-specific retrograde tracing, whole-cell patch-clamp recordings and post hoc

297 MnR afferents by combining retrograde tract tracing with immunofluorescence and in situ hybridizatio

298 istochemistry, immunofluorescence and neural tracing with subunit B of cholera toxin (CTB), we analys

299 Genetic tracing with UCP1-cre, however, indicated nearly half of

300 diogram was profoundly changed from previous tracings, with marked and diffuse voltage reduction (QS