ライフサイエンスコーパス: from one @3 to another

1 o assess the transfer of miR-143 and miR-145 from one cell type to another.

2 ch cortical electroencephalographic activity from one state to another.

3 ffects on IgE sensitization profiles already from one to another generation.

4 xtrapolations from one scale to another, and from one force to another, across different materials an

5 ments are gained or lost to vary in time and from one lineage to another.

6 tween sister chromatids, homologue pairs and from one metaphase spread to another.

7 d to another, from one grid to the next, and from one type of specimen to another, motivates a recons

8 facilitates the exogenous transfer of AnxA2 from one cell to another.

9 ncerted phase shift of molluscan assemblages from one well-defined regime to another.

10 describing spreading of fibrillar assemblies from one cell to another, in cell cultures, animal model

11 alized as a system for redirecting attention from one object to another, recent evidence suggests a m

12 o criterion expected when shifting attention from one perceptual dimension to another.

13 Transplanting gut bacteria from one mouse strain to another can override genetics a

14 eractions in the protein can tip the balance from one monomer fold to another.

15 ate that extrapolation of data on DC biology from one species to another has to be done with care, an

16 ty to reconfigure elementary building blocks from one structure to another is key to many biological

17 n networks needed to maintain stable bridges from one adhesive region to another.

18 ating the movement of various types of cargo from one cellular compartment to another.

19 their contents, thereby transferring cargoes from one cell to another.

20 ransfer of a rather localized charge carrier from one site to another triggers a deformation of the m

21 Reprogramming somatic cells from one cell fate to another can generate specific neur

22 s argue that in NHL an efflux of tumor cells from one disease site to another, distant site in which

23 allow serial transplantations of tumor cells from one fish to another without sublethal gamma-irradia

24 However, direct conversion of cells from one lineage to another often yields incompletely re

25 Metastasis, the movement of cancer cells from one site to another, involves remodeling of the cyt

26 tion factors can convert adult somatic cells from one type to another.

27 facilitating transfer of a dodecanoyl chain from one acyl carrier protein to another en route to the

28 These conditions also change from one birth cohort to another: some generations suffe

29 zones in which both species undergo a change from one color pattern form to another.

30 s that have the ability to reversibly change from one colour state to another with the application of

31 Somatic cells that change from one mature phenotype to another exhibit the propert

32 here the specificity determinants may change from one substrate to another.

33 ornaments and symbolic markings, the change from one way of living to another was not restricted to

34 The variation of changes from one eye to another implies that patients selected f

35 ear subject to regime shifts--abrupt changes from one state to another after crossing a threshold or

36 e underlying complex system abruptly changes from one state to another in a highly discontinuous fash

37 that the changes in free energy on changing from one aryl group to another, in either the acyl group

38 Changing from one crystal structure to another involves a phase t

39 otion is driven by the transfer of chirality from one Weyl node to another, rather than momentum tran

40 he chromosome to relay the partition complex from one DNA region to another across a ParA-ATP dimer g

41 g as genes, by templating their conformation from one molecule to another in analogy to DNA templatin

42 cilitatory interactions, varied considerably from one neuron to another.

43 The width varied considerably from one ring to another, but each ring maintained a con

44 hannels for direct transmission of contagion from one bank to another: liquidity hoarding, asset pric

45 Conversion from one land use to another caused significant increase

46 Lineage conversion from one somatic cell type to another is an attractive a

47 s are like Transformer toys, being converted from one enzyme type to another in the presence of the p

48 hene)s could readily be reversibly converted from one polymorph to another by appropriate processing

49 nsdifferentiation, the process of converting from one cell type to another without going through a pl

50 ration (AMD) does not follow the same course from one case to another and that phenotyping may be imp

51 iple routes a population can follow to cross from one adaptive peak to another.

52 entation (continuous) and those that crossed from one representation to another (discontinuous) were

53 tial cusps in GFA are observed when crossing from one crystallization pathway to another.

54 on due to varying sampling/sequencing depths from one sample to another.

55 Population structure may differ from one genomic region to another due to the variabilit

56 l that the LN distribution parameters differ from one mixture type to another and that important info

57 rengths and weaknesses of each method differ from one study to another; we provide an overview of the

58 tudy shows that CD3 expression levels differ from one T cell subset to another.

59 y which Hog1 regulates their activity differ from one to another.

60 nomic variables were significantly different from one model to another (P < 0.001).

61 SBUs having one kind of metal but different from one SBU to another, perform better than the sum of

62 of these phagocytes is strikingly different from one subset to another, with some cells derived from

63 erentiation and the rates of differentiation from one stage to another for different strains from 4%

64 ical assumptions where larvae simply diffuse from one site to another or where complex connectivity p

65 wing trapping states, facilitating diffusion from one of these states to another, in a fashion that i

66 al interfaces can relay information directly from one brain to another using a computer as a medium,

67 ere organisms are allowed to travel directly from one location to another, have relatively thin tails

68 the transfer of plasmid and chromosomal DNA from one bacterium to another during conjugation.

69 e is conjugation, the direct transfer of DNA from one cell to another.

70 The movement of nuclear DNA from one vascular plant species to another in the absenc

71 iation and association of the POU(HD) domain from one DNA molecule to another.

72 l to appropriately translate the drug dosage from one animal species to another.

73 e from central tolerance by receptor editing from one IgH allele to another was not a major mechanism

74 r state produced by transferring an electron from one base to another.

75 tion-oxidation reactions, carrying electrons from one reaction to another, and as a cosubstrate for o

76 ct as molecular machines that convert energy from one form to another through cycles of conformationa

77 likely to be ill-defined or jump erratically from one strain to another as an animal's genome is trav

78 ge varies from organism to organism and even from one growth stage to another.

79 long-scale correlations over slow evolution from one round-trip to another.

80 d to generate a matrix of observed exchanges from one enzyme function to another, revealing the scale

81 The quantity of STING and CD9 exported from one cell line to another was inoculum-size-dependen

82 d marked differences in risks of Pb exposure from one consumer home to another as a function of flow

83 s is nearly exhausted and that extrapolation from one receptor to another is as likely to be misleadi

84 The results enable extrapolations from one scale to another, and from one force to another

85 stage and benefits of regression of fibrosis from one stage to another.

86 oints at which complex systems abruptly flip from one state to another is one of the remaining challe

87 functional modules, or how information flows from one module to another.

88 st probable, or optimal path of fluctuations from one ordered state to another in real and synthetic

89 y rather than moving their attentional focus from one location to another.

90 shells undergo rapid snapping motion to fold from one stable configuration to another.

91 ns often differed significantly in frequency from one population to another, particularly in comparis

92 show that cortical areas can change function from one sensory modality to another.

93 can lead to an increased variability of gait from one step to another, raising the likelihood of fall

94 erous competing stimuli by moving their gaze from one object to another, in a rapid series of eye mov

95 representations, which allow generalization from one situation to another through their shared featu

96 question is whether these models generalize from one choice context to another.

97 n species can lead to introgression of genes from one species to another, providing a potential mecha

98 etween the two ways the parasite uses to get from one location to another is essential.

99 he reported effect sizes have varied greatly from one study to another.

100 uch as phosphate, acetyl and glycosyl groups from one protein to another protein.

101 terminus and the global transformation of H4 from one acetylation state to another following treatmen

102 versible event whereby TSG-6 can shuffle HCs from one HA molecule to another.

103 hroughput screening hits or scaffold hopping from one hit to another attractive series.

104 information directly rather than indirectly from one cortical area to another.

105 of the linkers in passing signal information from one domain to another.

106 Sequential dissemination of information from one enzyme to another facilitates signal transducti

107 ultiple eye movements is to pass information from one set of neurons to another around the time of ea

108 to relay the passage of genetic information from one site to another within a cell, ensuring that th

109 a continuous manner, thus allowing invasion from one 3D matrix to another, and (2) establish distinc

110 are known to shift abruptly and irreversibly from one state to another when they are forced across cr

111 UvrA also was observed jumping from one DNA molecule to another over approximately 1 mi

112 the terminal -CH2-NH3(+) group, due to jumps from one anionic surface group to another.

113 ch information is learned can shift learning from one brain system to another.

114 e brain's ability to transfer motor learning from one context to another, occurs in a wide range of c

115 so indicate that the spread of these lesions from one site to another is mediated by the cellular upt

116 be exercised in not overgeneralising lessons from one target group to another; (7) there is a clear n

117 cular carriers transport proteins and lipids from one organelle to another, recognizing specific iden

118 onstrate that LDs grow by transfer of lipids from one organelle to another.

119 tic rates varying over 2 orders of magnitude from one second to another.

120 elative metabolic flux pattern is maintained from one state to another, and that cells adapt to pertu

121 uming an initial stage for metaphor mappings from one concept to another and that these mappings are

122 ring bacterial conjugation, genetic material from one cell is transferred to another as single-strand

123 or functions other than transfer of material from one plastid to another.

124 e parabiosed mice, to study tumor metastasis from one parabiont to another, or to investigate the rol

125 mately 200 nm/s; (ii) nucleocapsids migrated from one actin filament to another at approximately 400

126 ctly undergo hydroformylation upon migration from one catalytic interface to another.

127 en developed to convert computational models from one format to another.

128 r enough to suggest that transferring models from one location to another without re-training is feas

129 tations, as a pattern is gradually "morphed" from one stored pattern to another, a sharp transition b

130 Infectious virus cores can move from one cell to another without budding and release of

131 Infectious virus cores can move from one cell to another without budding and release of

132 etwork properties change as synesthetes move from one condition to another.

133 efined segments of DNA that are able to move from one genomic location to another.

134 While proteins move from one location to another and can localize to multipl

135 his work, typical genes were thought to move from one position to another infrequently.

136 MinCDE most often moved from one branch to another in an invariant order, follow

137 s expressing PRRSV receptors, GFP-nsp2 moved from one cell to another through nanotubes in the presen

138 As rats moved from one environment to another, tonic neuron ensemble a

139 ed that the silencing trigger could be moved from one host to another using the parasite as a physiol

140 by viral reverse transcriptase (RT) is moved from one RNA template position to another.

141 ng molecules, plant miRNAs can also be moved from one tissue to another through the vascular system.

142 n post-transplantation events drive movement from one post-transplantation state to another and influ

143 ates and cause-specific hazards for movement from one state to another.

144 udes and orientations often vary when moving from one bone to another, across a craniofacial suture.

145 ve as direct intercellular signals by moving from one cell to another, playing crucial roles in tissu

146 tagged NS1 of IAV shows viral protein moving from one cell to another through an intercellular connec

147 kton switched rapidly (generally in <0.5 My) from one mode to another in response to environmental ch

148 are typically mobile entities, moving nests from one location to another throughout the life of a co

149 ed distribution of effort to steer a network from one state to another.

150 essing by shifting externally stable objects from one retinal location to another.

151 verted from nonfluorescent to fluorescent or from one color to another by illumination, and calcium i

152 nslating evidence-based detection parameters from one manufacturer to another.

153 tracted before single-stranded DNA is passed from one cell to another, it has recently been reported

154 croband electrodes, the tracer may be passed from one stationary position to another by rapidly reloc

155 nto subtasks in which the material is passed from one worker to another.

156 equence space we explore the mutational path from one fold to another.

157 ical system reconfigures by following a path from one state to another; this path, often a collection

158 along some particular high probability paths from one HDZ to another.

159 al experiments indicated that in the pathway from one equilibrium morphology to another, large compou

160 evidence for functional retargeting of PDE5 from one compartment to another, revealing a role for na

161 pathways and roles as the disease progresses from one stage to another.

162 a given brain region or control projections from one region to another (e.g., hippocampal-cortical o

163 pecific D3 structural changes are propagated from one membrane-bound monomer to another.

164 w perceptions of risk change when propagated from one person to another and what impact the repeated

165 -distance horizontal dispersal of propagules from one shallow reef to another.

166 rgo-bearing vesicles that transport proteins from one compartment to another.

167 ach is based on the simple idea of "punting" from one method to another using a learned threshold.

168 ed the surprising behavior of moving quickly from one possible position to another.

169 mosomal cohesin enables Scc2 to move rapidly from one chromosomal cohesin complex to another, perform

170 Spillover of reactants from one active site to another is important in heteroge

171 ogy is robust and can be transferred readily from one institution to another without loss of reproduc

172 mechanisms is critical for cells to relocate from one tissue to another.

173 Introducing shape-recognizing residues from one Hox protein to another swapped binding specific

174 sidase) activities that graft sugar residues from one xyloglucan oligosaccharide to another.

175 r, due to the variability of immune response from one individual to another and depending on the type

176 e stimuli, flexibly flipping their responses from one predictive stimulus to another.

177 the ability to flexibly shift fear responses from one stimulus to another if a once-threatening stimu

178 ithin the same interface and to pass results from one to another.

179 Translation of a macrocyclic ring from one station to another on a molecular thread is ini

180 of baseline and supplemental doses, rotation from one drug to another in poorly responsive patients,

181 We show that depending on the route from one state to another, action potential alternans an

182 We show that the evolution of RP from one stage to another often requires the failure of

183 ch string of interest to navigate seamlessly from one area to another.

184 However, many signals are constantly sent from one pathway to another, essentially linking all pat

185 nknown sensors and unidentified signals sent from one tissue to another which need to be identified.

186 Does information flow sequentially from one cortical area to another, or do networks of int

187 do proteins efficiently and precisely shift from one conformation to another?

188 sity, the polarity of which could be shifted from one session to another.

189 different phases of the burst can be shifted from one slow variable to another by changing a model pa

190 to be unidirectionally pumped (or 'shifted') from one magnetic layer to another.

191 complex models with punctuations and shifts from one evolutionary mode to another.

192 Subsequently, Isl1/Lhx3 binding shifts from one set of targets to another, controlling regulato

193 Ecosystems can undergo dramatic shifts from one stable state to another.

194 formation regulation by propagating a signal from one site to another distal site.

195 spanning microelectrodes that carry signals from one circuit element to another are needed for many

196 "higher order" nuclei that transfer signals from one cortical area to another.

197 to derive and then transfer gene-signatures from one analytical platform to another.

198 ions on EPS molecules may vary significantly from one bacterial species to another, thus it is crucia

199 , biological properties differ significantly from one clone to another in terms of virulence and host

200 the literature sometimes vary significantly from one measurement technique to another.

201 o-Gb3 and its analogues in plasma is similar from one individual to another in the same group of Fabr

202 Translocation of Sox2 from one specific DNA site to another occurs via jumping

203 at is essential for Lewy pathology to spread from one brain region to another.

204 genes enables regulatory influence to spread from one gene to another, suggesting that CTCF and BRD2

205 , once formed, proteopathic seeds can spread from one locale to another via cellular uptake, transpor

206 tionship between two agents to remain stable from one conflict to another.

207 asks such as transporting a mechanical state from one location to another.

208 ctron reduction to H2O2 varies substantially from one medium to another for a given catalyst.

209 (called metabolons) that channel substrates from one enzyme to another, but there has been no experi

210 ing phenomena, and how the system can switch from one branching pattern to another using low-dimensio

211 lity can cause cells to spontaneously switch from one phenotype to another.

212 reconfiguring the system fluidics to switch from one probe to another.

213 NA chain from which it is synthesized switch from one RNA template to another.

214 r gene-expression state, and how they switch from one stable state to another.

215 In addition, Purkinje neurons could switch from one state to another spontaneously or with current

216 ls inhabit different environments and switch from one to another.

217 ant devaluation tasks, but not when switched from one Pavlovian devaluation task to another Pavlovian

218 achieve remission when treatment is switched from one to another of these drugs.

219 well characterized the frequency of switches from one host to another remains obscure.

220 ichia coli cell with the lac operon switches from one phenotype to another.

221 ement initiation and execution, and switches from one state to another.

222 l chemistry, and addressing it, by switching from one chemistry to another by controlling an external

223 ooked at survival in rodents after switching from one diet to another, the underlying mechanisms of t

224 Forty-five episodes involved switching from one ISA to another, with 50% to 100% of these patie

225 ding, generating colorful spectral switching from one spectral type to another.

226 stems have to make decisions about switching from one state to another.

227 another, learning was unblocked by switching from one to another equally valued reward, a manipulatio

228 y parameter perturbation to drive the system from one attractor to another, assuming that the former

229 is more than twice as fast as the jump time from one hydrogen-bonded configuration to another in bul

230 transfer large amounts of a patient's tissue from one location used to another in order to restore ph

231 g is to transit the drug and molecule tokens from one node or place to another, and blasting is to re

232 Gene conversion, non-reciprocal transfer from one homologous sequence to another, is a major forc

233 tients in the United States require transfer from one hospital to another for acute myocardial infarc

234 cells, migrate across barriers, and transfer from one host to another.

235 specializes in substance and signal transfer from one immune cell to another.

236 uman behavior, but how chemosignals transfer from one individual to another is unknown.

237 The transfer from one point to another point in the environment, as w

238 This complex phenomenon of electron transfer from one radical to another has been investigated in pro

239 hat the mtSSB tetramer can directly transfer from one ssDNA molecule to another via an intermediate w

240 o provide the first example of heme transfer from one surface protein to another surface protein in G

241 ackaging function allows convenient transfer from one user to another of the dChip software, microarr

242 how grasp-related information is transferred from one area to another.

243 process by which plasmid DNA is transferred from one bacterium to another, is mediated by type IV se

244 n optical format can be directly transferred from one beam to another without converting back to the

245 structure when A. marginale was transferred from one cell-type to another, suggesting that the expre

246 d gross functions can be readily transferred from one protein to another by transplanting large block

247 yntrophic communities, energy is transferred from one species to another, either through direct conta

248 y successive losses, or horizontal transfers from one lineage to another through intron homing or rev

249 chemical reaction during the transformation from one doped material to another and the consequent ef

250 mming memory T cells (i.e., a transformation from one type of immunity to another, for example, regul

251 Materials can be transformed from one crystalline phase to another by using an electr

252 ed transposition of the integrated transgene from one chromosomal locus to another.

253 A residue's complete transit from one Ramachandran basin to another, however, occurs

254 directional emission such that by transiting from one EP to another one the direction of emission can

255 , the human brain must seamlessly transition from one brain state to another, in the process drawing

256 point to the difficulties for the transition from one homogeneous system (RNA) to another (RNA/DNA) i

257 We observed a transition from one isomeric protein configuration to another after

258 ic distal ileum, thus driving the transition from one microbial community structure to another.

259 ptive design allowed for seamless transition from one phase to another, and central venous catheter u

260 he aim of understanding how cells transition from one state to another.

261 is identifying the propensity to transition from one steady state to another, which in practice can

262 olved efficient strategies for transitioning from one cell to another in a process termed intercellul

263 The probability of transitioning from one health state to another, reinfection rates, in-

264 ng the annual probabilities of transitioning from one state to another, and present case estimates fo

265 pathway and capturing successful transitions from one care modality to another.

266 important to learn how to drive transitions from one phase to another.

267 urvature, combine to allow rapid transitions from one stable state to another.

268 odox and post-transition), their transitions from one state to another as well as their interaction w

269 In particular, translation from one phase to another, which occurs at the critical

270 The probe, which translocates from one anchor site to another, mimicking motor protein

271 hin the pericellular matrix by translocating from one HS-binding site to another.

272 that if an intervention reduces transmission from one host to another by a constant factor, then its

273 h the aim of preventing malaria transmission from one infected individual to another.

274 s and propagate like prions when transmitted from one individual host to another.

275 eneral mechanism by which populations travel from one adaptive peak to another.

276 of the distribution and propagation of twist from one DNA linker to another for a two-nucleosome arra

277 on is extremely similar in a given cell type from one individual to another.

278 not address the heterogeneity of cell types from one CNS region to another and are complicated by al

279 resumably, are thought to vary unpredictably from one mutation to another.

280 an 20%, but there is significant variability from one person to another, indicating that while some o

281 ughout life, but neuroplasticity is variable from one brain system to another.

282 We show that there can be huge variations from one experiment to another, and that there may also

283 Integrity of the choroid varied from one eye to another and was not related strictly to

284 This helicity varies from one bZIP-bR to another despite a significant sequen

285 The amplitude of rocking varies from one crystal form to another and is correlated with

286 identity of the core-forming segments varies from one polymorph to another, a phenomenon known as seg

287 The extent of activation varies from one promoter to another and is only poorly correlat

288 obability that a zygote will be male, varies from one zygote to another within litters, thus constitu

289 is case dependent and the solution can vary from one application to another.

290 hat drive or accompany the pathogenesis vary from one CNV to another.

291 ed by a large number of mechanisms that vary from one kinase to another.

292 Regulatory pathways of plasticity may vary from one set of environments to another due to unique fe

293 Quorum-controlled activities vary from one species to another.

294 ions among individuals are debated, and vary from one species to another.

295 nteractions between equivalent CG pairs vary from one subunit to another.

296 The Foxp3 levels vary from one Treg clone to another and are significantly low

297 imple conduits that passively transfer virus from one individual to another.

298 ined for any given species but varies widely from one species to another.

299 lar to the number found when comparing words from one random model to another.

300 rate constant for direct transfer of Zif268 from one target site to another.