ライフサイエンスコーパス: trace

1 strength meet, they are annihilated without trace.

2 atabases and a large dataset of mobile phone traces.

3 slowly degrade molecular and cellular memory traces.

4 bserved as clear steps in the bubble-closing traces.

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

6 l aspect of the prostatic urethra by lineage tracing.

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

8 Here, we trace a comprehensive picture of the excitonic process i

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

10 anding and analyses of current-voltage (I-V) traces across molecular junctions.

11 We purified trace-active derivatives of kynurenine and identified tw

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

13 gen labelling (PAL) and Voluntary Incidental Trace Allergen Labelling (VITAL((R)) ) tools were design

14 Trace amine-associated receptor 1 (TAAR1) agonists have

15 Trace amine-associated receptor 1 (TAAR1) is a highly co

16 of monoamines results from the production of trace amines (such as tryptamine) by pericytes that ecto

17 acid decarboxylase (AADC), which synthesizes trace amines directly from dietary amino acids (such as

18 protein-coupled receptor bound by endogenous trace amines.

19 nerated a mixture of G1 and G2, as well as a trace amount of insoluble polymer-like precipitate.

20 Dissolution of CaCO3, present in trace amounts in India bauxite, significantly hindered f

21 n state after citrate coordination, although trace amounts of Au(delta)(+) are observed.

22 brium as shown between oxoammonium salts and trace amounts of corresponding nitroxide.

23 d to produce monoterpene in tobacco but only trace amounts of monoterpenes have been detected.

24 Expression of trace amounts of mutant proteins from NMD-competent PTC-

25 rom a contemporary ocean that contained only trace amounts of sulfate remains controversial.

26 d the crystallisation history of Toba quartz traces an influx of a low-delta(18)O component into the

27 However, trace analysis in the presence of a dominating component

28 can be applied as a suitable alternative for trace analysis of copper.

29 fabricable SERS platforms for ultrasensitive trace analysis.

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

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

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

33 ials, to the concentration and separation of trace analytes in liquid-liquid microextraction.

34 continuous and completely automated process trace analytics exemplified for the analysis of a CO2 st

35 as performed on the powder X-ray diffraction traces and showed that the higher concentration of monoc

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

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

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

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

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

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

42 inetic schemes from experimental macroscopic traces, and we anticipate that it may be useful in the s

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

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

45 orus content, but had little effect on other trace- and macro-nutrient elements in the rice bran.

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

47 We traced association signals in 200-kb regions surrounding

48 encies above 5% and cassette function can be traced at the genomic DNA and the mRNA level.

49 on the genetic pedigrees, many blocks can be traced back to a well-known Strampelli cross, which was

50 Thus, GFP fluorescence is traced back to an intrinsic chromophore property, and by

51 we report that these seed phenotypes can be traced back to defective embryogenesis.

52 This could be traced back to disrupted cell-cycle kinetics and a prema

53 the microbiome's functional capacity can be traced back to specific taxa.

54 The initial steps in this process can be traced back to the dispersal of farming groups into the

55 ithin a basement membrane, and can always be traced back to the renal artery.

56 Their origin may be traced back to their intricate relationships governing r

57 Trace-back investigation identified a common flour-produ

58 from experimental labelling, and those that trace backwards across the life history of an organism.

59 ry C neurons in the N/J ganglia retrogradely traced by 1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarb

60 chomatis infection after having been contact-traced by a chlamydia-positive partner were more likely

61 We included 98 women who were contact-traced by C. trachomatis-positive sex partners at the ST

62 with N-ethylmaleimide, and the reactions are traced by high resolution mass spectrometry and nuclear

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

64 Alternative interpretations of the trace call had little effect on these ratios.

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

66 Retrograde tracing combined with single-cell mRNA amplification ind

67 FS interpretation complicate the analysis of trace concentrations of impurities that are distributed

68 Monitoring and determination of ultra-trace concentrations of monoamine neurotransmitter such

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

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

71 ining came to withhold responding during the trace-conditioned cue, responding less than for another

72 rtance of cholinergic modulation in mPFC for trace conditioning and show that the observed effects ca

73 prefrontal cortex (mPFC) impaired appetitive trace conditioning at a 2 s trace interval.

74 test this, mice were trained on a Pavlovian trace conditioning procedure in which the presentation o

75 copolamine was without effect in an aversive trace conditioning procedure, but impaired appetitive co

76 ade of muscarinic receptors in mPFC impaired trace conditioning shows that these receptors are critic

77 Trace conditioning was similarly impaired at the 2 s tra

78 necessary to condition their association in "trace conditioning." The present study used conditioning

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

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

81 studies suggest the reaction is catalyzed by trace copper salts and that a Z- to E-hydrazone isomeriz

82 owever, the mechanisms by which motor memory traces develop during sleep remain controversial in huma

83 igate potential interactions with respect to trace dominance, strengthening, and interference associa

84 data with drift originating from one or many traces (e.g., Forster resonance energy transfer).

85 r reports a nanometer-scale investigation of trace element (As, Ca, Cr, Cu, Fe, Mn, Ni, S and Zn) dis

86 ow-dose mapping of beam-sensitive specimens, trace element analysis, and time-resolved spectroscopy.

87 tegrated zircon isotope (U-Pb, Lu-Hf, O) and trace element dataset from the paired Cu-Au (copper) and

88 -ray nanofluorescence was applied to map the trace element distributions in selected areas of the roo

89 Copper is an essential yet potentially toxic trace element that is required by all aerobic organisms.

90 distributions of Selenium (Se), an essential trace element that is required for humans.

91 we present iron-speciation, redox-sensitive trace element, and nitrogen isotope data from a Neoprote

92 ze, and control this biochemically versatile trace element.

93 n at the base of the Pilbara Supergroup have trace-element compositions that are consistent with thes

94 to determine both total and bioaccessible of trace elements and heavy metals (Cd, Cr, Cu, Co, Al, Zn,

95 Both the trace elements and minerals levels in the 4-6months vege

96 ly, these TTGs have 'arc-like' signatures of trace elements and thus resemble the continental crust p

97 take and accumulation of coexisting ENPs and trace elements by soybeans and to gain insights into the

98 However, the content of trace elements can be adjusted by cultivation conditions

99 The characterization of trace elements in minerals using extended X-ray absorpti

100 be identified as a source of Se and of other trace elements in precipitation samples.

101 (usually diarrhea), interactions with other trace elements such as copper and zinc, altered gut micr

102 We use the correlations of CO2 with trace elements to define an average carbon abundance for

103 Removal of toxic trace elements via adsorption onto iron oxides is an ine

104 The profile of 18 trace elements was traced in 68 milk samples collected f

105 ions to Se distributions suggests that other trace elements with similar retention mechanisms will be

106 ater contamination "fingerprint" analysis of trace elements, revealed that the immediate cause of the

107 are expected to remain an effective sink for trace elements.

108 s of the minerals: Ca, K, Mg, Na, P, and the trace elements: Cd, Cu, Fe, Mn, Ni, Pb, Se, Zn were dete

109 ndestine graves, and obtaining soil and skin trace evidence.

110 rning to investigate how newly-formed memory traces evolve dynamically over time.

111 Importantly, we demonstrate that trace exogenous chemicals can be detected in fingerprint

112 A cell tracing experiment was included to observe the preservat

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

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

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

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

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

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

119 Lineage-tracing experiments revealed that the cells that accumul

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

121 closely related condensation products, named trace-extended aromatic condensation products (TEACOPs),

122 molecular techniques, we determined whether trace fear conditioning and extinction engages the SR/D-

123 In this study, mice underwent trace fear conditioning consisting of an auditory CS pai

124 Parallel trace fear conditioning experiments showed that spine lo

125 Here, we show that trace fear memory undergoes a protein synthesis-dependen

126 sult in a long-lasting and meaningful memory trace for the event but, at the same time, make it diffi

127 When we analyze 2019 mutant traces for 17 different RNAs, we find that features of t

128 ormation, the creation and storage of memory traces for spatial information, and the use of spatial i

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

130 item is sufficient to wipe the corresponding trace from the hidden state.

131 Furthermore, ERG traces from regenerated retinas displayed waveforms matc

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

133 e lasers (ICLs) is a sensitive technique for trace gas sensing.

134 ations, and it is an important ocean-derived trace gas that contributes to the iodine burden of the a

135 Molecular hydrogen (H2 ) is an atmospheric trace gas with a large microbe-mediated soil sink, yet c

136 Nitrous oxide (N2O) is a climate relevant trace gas, and its production in the ocean generally inc

137 the quartz tuning fork (QTF) as well as the trace-gas concentration can be obtained simultaneously b

138 be used for ultra-sensitive calibration-free trace-gas detection and fast spectral scan applications.

139 + RO2), determines the lifetimes of reduced trace gases such as methane and the production of partic

140 treme enrichment of photochemically produced trace gases.

141 Here we trace gene-content evolution of Y-chromosomes across 22

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

143 Child contact tracing has been widely recommended but poorly implement

144 We trace here the major findings leading first to the hypot

145 We traced heritable L1 insertions to pluripotent embryonic

146 oliated carbon nitride, which liberates only trace hydrogen levels when photoexcited directly, does n

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

148 The profile of 18 trace elements was traced in 68 milk samples collected from buffalo farms i

149 dispersals, which left at least some genetic traces in modern populations, indicate that later replac

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

151 The unique role of KO(t)Bu is traced, in part, to the stabilization of crucial interme

152 h as the working memory required to bridge a trace interval in associative leaning.

153 ut impaired appetitive conditioning at a 2 s trace interval.

154 aired appetitive trace conditioning at a 2 s trace interval.

155 Tracing interventions increase reengagement, but develop

156 Detecting and characterizing these molecular traces is necessary to understand the environmental impa

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

158 European culture traces its history back to the ancient Greek civilisatio

159 ly measurable changes in output current that trace Langmuir isotherms within error of those seen in s

160 Determination of trace level concentrations of cadmium, copper, lead, and

161 l samples on a polymer specific mass related trace level.

162 redox species, suggesting the possibility of trace-level analysis.

163 d quantification of 15 pesticide residues at trace levels in cabbage, broccoli, cauliflower, lettuce,

164 sitivities and are capable of discriminating trace levels of cholera toxin on a supported lipid membr

165 t also demonstrated excellent sensitivity to trace levels of Gram-negative bacteria, while remaining

166 sensor for the simultaneous determination of trace levels of heavy metal ions by anodic stripping vol

167 Plants require trace levels of manganese (Mn) for survival, as it is an

168 hod is suitable for routine determination of trace levels of TA and was applied to 26 different buckw

169 Only trace levels of the known toxic metabolite, thio-DMA, we

170 tracking, with attention both to those that trace lineage forwards from experimental labelling, and

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

172 regardless of drift or states visited across traces-may now be treated on an equal footing, thereby e

173 rth Sea, Germany, and linked our findings to trace metal and nutrient concentrations.

174 At each site, trace metal concentrations as well as enrichment factors

175 N2 -fixing A. vinelandii under a variety of trace metal conditions.

176 Thus, modern assessments of trace metal contamination cannot ignore early industrial

177 de minerals (phyllomanganates) often control trace metal fate in natural systems.

178 cent increase in observational data for this trace metal has challenged the prevailing view of the oc

179 Sulfurization may affect DOM-trace metal interactions, including complexation and met

180 Early industrial trace metal loadings are poorly characterized but potent

181 sediment below the SWI, defined by elevated trace metal mobilization.

182 Fe(II)-catalyzed mineral transformations and trace metal(loid) release.

183 ships show that atmospheric contamination by trace metals (Ag, Cd, Sb, Tl, but also V, Ni, and Mo whi

184 rized but potentially substantial sources of trace metals to the landscape.

185 system has not mobilized naturally occurring trace metals, including arsenic, chromium, cobalt, nicke

186 is a complex chemical mixture consisting of trace metals, organic compounds, and often, high levels

187 which influences the reactivity of DOM with trace metals.

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

189 PM2.5-bound trace microbial elements, such as lipopolysaccharide may

190 Trace minerals (TM) play a role in skin integrity and wo

191 17.4 months for severe, moderate, mild, and trace mitral regurgitation, respectively, with 20% of pr

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

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

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

195 one or two steps, we semisynthesized the six trace natural compounds 1-6 and a series of derivatives

196 hile leaving permanent genetic access to the traced network.

197 Molybdenum (Mo) is an essential trace nutrient but has negative health effects at high c

198 r and exchange coupling to simulate the time traces obtained in a double electron electron resonance

199 1 populations appeared to participate in the trace of the percept of stimulus 1 as the rat awaited st

200 ld be used for the infield identification of traces of body fluids and to obtain phenotypic informati

201 od, and invalidates older studies that found traces of Cr(VI) in food by using a less specific off-li

202 of ancient mammalian DNA that often includes traces of hominin DNA, even at sites and in layers where

203 No traces of imidazo[1,5-a]pyridine derivatives were obtain

204 Besides occasional traces of methylarsonic acid (MA), the arsenic speciatio

205 ted silicon species as detected by IR, or by traces of oxygen which can generate a reactive peroxide

206 redominant Neolithic background, we identify traces of Post-Neolithic Levantine- and Caucasus-related

207 mposition Al73Ni19Fe4Cu2Mg0.6Mo0.4Mn0.3 with traces of Si and Cr were found along the recovered inter

208 ) is a typical protecting group cleavable by traces of TFA.

209 ateral offset between the surface and mantle traces of the thrust system reveals a steep boundary, in

210 al-time simultaneous deconvolution of O(105) traces of whole-brain larval zebrafish imaging data on a

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

212 We conducted anatomical tracing of mPFC projections and optogenetic interrogatio

213 Epidemiological contact tracing of patients and Bayesian phylogenetic analysis o

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

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

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

217 Tracing of Troy(+) cells during nephrogenesis demonstrat

218 The lowest trace oil content in the retentate was 3.6 mg L(-1), and

219 ation and the statistics of the trajectories traced on the board.

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

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

222 also be easy to dispose of so as to leave no trace, or have a detrimental effect on the environment.

223 phylotranscriptomic analyses can be used to trace organ evolution in the deep history of plant speci

224 ith infrared spectroscopy (AFM-IR) to detect trace organic and inorganic species and probe intraparti

225 Beta-trace protein (BTP), a monomeric glycoprotein, is known

226 Of these patients, 55.7% had none-trace PVR, 32.6% had mild, 8.2% had mild to moderate, an

227 ate (CPP), lavandulyl diphosphate (LPP), and trace quantities of maconelliyl diphosphate (MPP) from t

228 d, hesperidin and naringenin were present in trace quantities.

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

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

231 A key advantage of this method is that all traces-regardless of drift or states visited across trac

232 ch as drift), common to single molecule time traces, result in an overinterpretation of drift and the

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

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

235 fully applied for the determination of ultra-trace RIF amounts in biological and pharmaceutical sampl

236 footing, thereby eliminating user-dependent trace selection (based on drift levels), preprocessing t

237 nditioning was similarly impaired at the 2 s trace (shown as reduced responding to the CS and during

238 Ray tracing simulations support the measurement results.

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

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

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

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

243 Tract tracing studies demonstrated that Ovvm is a major target

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

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

246 ycle feedbacks should consider weathering of trace sulfide minerals in addition to silicate minerals.

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

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

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

250 stral MADS domain protein reconstruction, we trace the evolution of organ identity quartets along the

251 We aimed to trace the geographic origin of HIV-1 infection for migra

252 lexed single-cell DNA sequencing approach to trace the metastatic lineages of two CRC patients with m

253 e use the dyW mouse model for human MDC1A to trace the onset of the disease during development in ute

254 zed micro X-ray computed tomography (mCT) to trace the profiles of the full complement of large ocell

255 We trace the rise of macrosystems ecology with respect to p

256 rom combustion sources, which can be used to trace the sources of ambient particles and to know their

257 Recent longitudinal studies have traced the emergence of bNAbs in HIV-1 infection, inspir

258 ishes mTOR as a central target in glioma and traces the failure of existing drugs to incomplete/nondu

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

260 By tracing the distribution of epialleles throughout the tu

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

262 Tracing the evolution of enzyme activity and stability f

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

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

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

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

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

268 investigates different strategies applied to trace these molecules.

269 rall 33-68% of these microorganisms could be traced to a marine origin, being transported thousands o

270 vided into four subfamilies, and each can be traced to ancestral members that contain a kinase domain

271 igh levels of exogenous sequence that can be traced to bacteria.

272 ronuclei formation, and fork protection were traced to the ability of GOF p53 to transactivate cyclin

273 suggests that many of these outcomes can be traced to the impacts of early adversity on multiple and

274 ulation of Cape Verde, whose Kriolu language traces to West African languages and Portuguese [29, 32-

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

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

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

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

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

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

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

282 Specifically, after a trace-to-delay update session, the amygdala is now requi

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

284 reorganize the neural circuit supporting the trace-trained memory, so that it better reflects the cir

285 Tracing transcriptional differences with a high spatial

286 cute coronary syndrome survivors enrolled in TRACE (Transitions, Risks and Actions in Coronary Events

287 mployed to investigate the immobilization of trace uranium associated with nanophase iron (oxyhydr)ox

288 ase were selected in the lateral nucleus and traced using Neurolucida software in their entirety.

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

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

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

292 maize, TRU1 is highly expressed in the leaf trace vasculature of axillary internodes, while in teosi

293 e development of HIV-1 resistance to PIs, we traced viral evolution under the pressure of PIs using G

294 From single-molecule spectral time traces, we further examine isomerization between the two

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

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

297 el system can be measured using current-time traces, which are straightforward to analyze.

298 Second, cholangiocytes were lineage traced with concurrent inhibition of hepatocyte prolifer

299 rsion of ultrashort optical pulse, which are traced with simple computation of ray-pulse matrix.

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