ライフサイエンスコーパス: transition from @2 to

1 n robust single-metal-node networks that can transition from 3D to 2D extended structures.

2 Further, an update on the transition from 2D to 3D cultures and current organoid (

3 ogression upon removal of MeCP2 in male mice transitions from 3 to 4 months to only several days, fol

4 Our results show that a transition from 2M- to 4M-zirconolite occurs with increa

5 solated during the last glacial-interglacial transition from approximately 15 to 9 ka.

6 tion of ubiquitinating factors may drive the transition from a complex to a simple proteome.

7 The Berezinskii-Kosterlitz-Thouless phase transition from a disordered to a quasi-ordered state, m

8 Thus, as cells transition from a dividing to a nondividing state, there

9 A transition from a high to a lower water concentration, f

10 NDH complex may increase the probability of transition from a photoautotrophic to a heterotrophic li

11 adation rates of long-lived proteins as they transition from a proliferating to a quiescent state.

12 rame, indicating the normative length of the transition from a right to a service is contextually dep

13 ble temperature resistivity studies reveal a transition from a semiconducting to a metallic phase wit

14 h rapid changes in climate led the forest to transition from a sink to a source of carbon.

15 Our results provide evidence that podocytes transition from a static to a dynamic state in vivo, she

16 rgy levels of the system as it undergoes the transition from a thermalized to a localized phase.

17 An increase in ionic strength induced a transition from a train to a loops and tails configurati

18 r (17.2 vs 1.6 per 100 person-years) for the transition from A(-)N(-) to A(-)N(+), three-times higher

19 pe (TEM) study revealed a similar structural transition from amorphous to a distorted rutile structur

20 undergoes a first order meta-magnetic phase transition from an antiferromagnet to a ferromagnet abov

21 homeostasis in the context of the vertebrate transition from an aquatic to a terrestrial lifestyle.

22 tion program that allows partial or complete transition from an epithelial to a mesenchymal state.

23 bypass the instability by inducing a smooth transition from an open to a closed bud.

24 frequency transverse phononic gap due to the transition from an oscillatory to a ballistic dynamic re

25 an control or inflamed specimens, indicating transition from flat to a deformed surface.

26 understanding of kinases that can block the transition from lineage commitment to a differentiating

27 ormula: see text], a dielectric material can transition from localization behavior to a band gap cros

28 hat this T c enhancement arises from a phase transition from pristine Bi2212 to a mixture of supercon

29 mination is protracted, with the growth cone transitioning from a dynamic to a static state.

30 We show that TIRAP PBM transitions from a disordered to a helical conformation

31 orphology of WBC subpopulations as a patient transitions from a healthy to a diseased state.

32 Upon binding Ro, the GluN2B ATD clamshell transitions from an open to a closed conformation.

33 to 2, the primary Fe(III) oxidation product transitions from lepidocrocite to a ferrihydrite/silica-

34 ohol, the neural mechanisms that mediate the transition from use to abuse are not fully understood.

35 We show that there is an abrupt transition from alkaline to acid soil pH that occurs at

36 small changes in water balance cause a steep transition from alkaline to acid soils across natural cl

37 The mechanisms behind the increased transition from latent to active TB in coinfected indivi

38 ns were transplanted from the 81 donors that transitioned from DCD to actual DBD, including 24 heart,

39 At 6 months subjects transitioned from study drug to ACZ.

40 ses interact with contextual factors to help transition from children's to adult services for young a

41 nd childhood, which means they must make the transition from children's to adult services.

42 e expression until hematopoietic progenitors transition from fetal to adult transcriptional states.

43 santhemum morifolium), results in precocious transition from juvenile to adult, as well as early flow

44 diac myocytes from the cell cycle during the transition from neonatal to adult stages.

45 replacement treatment are needed during the transition from paediatric to adult endocrine care, and

46 Influences on diet quality during the transition from adolescence to adulthood are understudie

47 /beta-catenin signaling is necessary for the transition from early to advanced pancreatic intraepithe

48 eneral, and about molecular details of their transition from soluble to aggregation-prone conformatio

49 The transition from noble metals to aluminum based antenna-r

50 The transition from prealveolar macrophage to alveolar macro

51 or recruitment of Pol III and to promote the transition from a closed to an open Pol III pre-initiati

52 dominant part of the protein population, the transition from a native to an amyloid-like structure oc

53 S-peptide undergoes a transition from intrinsic disorder to an ordered helical

54 served variations of delta(44/42)Ca record a transition from placental nutrition to an adult-like die

55 ion of insect pollinator associations in the transition from gymnosperm to angiosperm dominance.

56 lting steric effects can be mitigated by the transition from glycine bound to apo state of the GluN1

57 It remains to be determined what causes the transition from "physiological" to "apoptotic" UPR, but

58 We found the age-related transition from rhythmicity to arrhythmicity for each pa

59 The emergence of apomixis-the transition from sexual to asexual reproduction-is a prom

60 creasing order in cell motion causes a phase transition from symmetric to asymmetric body elongation.

61 The mechanisms mediating the transition from the migratory to bactericidal phenotype

62 Recombination is attributed primarily to transitions from mobile carriers to band-tail or deep tr

63 The peptide exhibits a conformational transition from random coil to beta-sheet by changing th

64 ichia coli and other bacteria, including the transition from planktonic to biofilm growth.

65 ols diverse functions in bacteria, including transitions from planktonic to biofilm lifestyles, virul

66 re-water element abundances revealed a rapid transition from abiotic to biotic signatures of weatheri

67 udying C. amylolentus will shed light on the transition from tetrapolar to bipolar mating systems in

68 lantation mouse embryos, where it blocks the transition from morula to blastocyst during embryonic de

69 in a complete block of P. yoelii plasmei2(-) transition from liver stage to blood stage infection in

70 addition, neurons in both of these cortices transition from responding to both tactile and auditory

71 ndamental driving force for the evolutionary transition from solitary living to breeding cooperativel

72 e's ordered and disordered phases revealed a transition from plastic deformation to brittle failure a

73 with shorter infection time, indicating the transition from narrow autologous to broad heterologous

74 es by the external field as well as a smooth transition from single stripe to bubble domains, which o

75 plored size regime allows us to identify the transition from molecular vibrations to bulk phonons in

76 from each dimension in both streams, with a transition from shape to category along the posterior-to

77 In particular, microglia contribute to the transition from acute pain to chronic pain, as inhibitio

78 gesting this pathway may be important in the transition from acute to chronic middle ear inflammation

79 t significantly expand their apical area and transition from a polygonal to circular apical shape to

80 To help facilitate the transition from concept to clinic, new research tools ar

81 ng near the blister crack tip, caused by the transition from membrane stretching to combined bending,

82 reveals the genetic hierarchy underlying the transition from progenitor to committed precursor, integ

83 levels in the amygdala may contribute to the transition from moderate to compulsive intake of cocaine

84 The inherently three-dimensional transition from bulk-turbulent to confined-coherent flow

85 content, the macrocycles undergo a stepwise transition from a cylindrical to conical shape.

86 CSE1L was significantly increased during the transition from AD to CRC when compared with NR in a CRC

87 s to the applied potential, and it shows the transition from overscreening to crowding of counterions

88 They also transitioned from disabled to dead earlier (adjusted HR,

89 icipants with >/=20 teeth had lower risks of transitioning from healthy to dead (adjusted HR, 0.58 [9

90 r RARgamma provides a key checkpoint for the transition from life to death.The molecular switch betwe

91 of the Fur, FsrA, and PerR regulons as cells transition from iron sufficiency to deficiency.

92 ond-bearing xenoliths and corresponds to the transition from coarse to deformed xenoliths.

93 proxy of health in countries that underwent transition from autocracy to democracy that lasted for a

94 bacterium Myxococcus xanthus, inhibiting the transition from growth to development when nutrients are

95 ghts into the processes of the shock-induced transition from graphite to diamond and uniquely resolve

96 6a limits RA pathway activity to control the transition from proliferation to differentiation in the

97 quired for Casparian strip formation and the transition from proliferation to differentiation in the

98 onal Theory (DFT) calculations show that the transition from indirect to direct bandgap in monolayer

99 The transition from nondirectional to directional force gene

100 etween twinning and strong shocks, we find a transition from twinning to dislocation-slip-dominated p

101 vity is thought to have been crucial for the transition from RNA to DNA genomes during the early hist

102 n-Arg-Gly-Asp-peptide affinity by 18% with a transition from single to double valency, consistent wit

103 e, temperature and strain rates regulate the transition from brittle to ductile behaviour.

104 When crown buds transitioned from endo- to ecodormancy, the ABA metaboli

105 with praziquantel increases in an attempt to transition from control to elimination of schistosomiasi

106 We also estimate 12 host transitions from bison to elk, and 5 from elk to bison.

107 on provides rate-limiting control during the transition from initiation to elongation which dictates

108 ion of RNA synthesis; rather, they block the transition from initiation to elongation, which is thoug

109 The transition from transcription initiation to elongation i

110 nding chromatin, cooperating to allow proper transition from transcription initiation to elongation.

111 In recent times, only HIV has made the transition from epidemic to endemic, but diseases that h

112 When UABs transitioned from para- to endodormancy, ABA and PA leve

113 ergetics played a direct, causal role in the transition from prokaryotes to eukaryotes and the subseq

114 BB expression, several marker genes for the transition from proliferation to expansion were highly u

115 onset of type 2 diabetes is characterized by transition from successful to failed insulin secretory c

116 The transition from antiferromagentism to ferromagnetism is

117 On the other hand, sudden transition from coarse-to-fine grain sizes promoted a ho

118 target mimic resulted in compact spikes and transition from glumes to florets in apical spikelets.

119 t apical meristem (SAM) is a hallmark of the transition from vegetative growth to flowering.

120 a state of AF/FM co-existence and shows the transition from AF to FM regions proceeds via nucleation

121 thermomagnetic behaviour consistent with the transition from AF to FM.

122 ws that, in the long run, Neolitization (the transition from foraging to food production) was associa

123 near amplifier that allows global climate to transition from deglacial to full interglacial condition

124 esolution allowing for investigations of the transition from proplastids to functional chloroplasts.

125 er retinotopic visual areas, implying that a transition from retinotopic to "functional" organization

126 y around origins in G1 is established during transition from G2/M to G1 in a pre-RC-dependent manner.

127 ge includes the well-known solid-solid phase transition from Ga-I to Ga-II at low temperature.

128 The transition from wakefulness to general anesthesia is wid

129 experience may be a strong predictor of the transition from normal to generalized fear expression.

130 As threat intensity increases, fear transitions from discriminative to generalized.

131 gulate RNP assembly, a step required for the transition from primary transcription to genome replicat

132 the ecology of the paddies, which triggers a transition from local to global-scale control of water s

133 These lines showed transitions from florets to glumes in the basal spikelet

134 Mitochondria guide the required transition from oxidative to glycolytic metabolism in nu

135 During the early stage, cells transition from growth-arrested to growing.

136 eation rate, the model predicts an explosive transition from stationary to growing asters with a disc

137 Furthermore, the transition from H3K9me2 to H3K9me3 is required for RNAi-

138 activated by a post-EMT marker, boosting the transition from low invasion to high invasion, as mediat

139 span the rising phase of incubation and the transition from low to high CP-AMPAR levels.

140 ated by the presented method reveal a smooth transition from low to high LETs which is an advantage o

141 the history of the Earth's atmosphere as it transitioned from anoxic to highly oxic (1-2 billion yea

142 echanism that was apparently lost during the transition from hemimetaboly to holometaboly.

143 Cognitive function changes during the transition from hospital to home after acute coronary sy

144 barrier height and the dephasing strength, a transition from coherent to hopping electron transport o

145 able, just as many countries are considering transitioning from cytology-based to HPV-based cervical

146 um and water uptake were up-regulated during transition from dormancy to hydration.

147 n changing the pH between 5 and 8, via phase transition from super hydrophilic to hydrophobic.

148 The fungal pathogen Candida albicans can transition from budding to hyphal growth, which promotes

149 ns also revealed that GaSb undergoes a phase transition from F-43m to Imma at 7.0 GPa and explained t

150 GPa, which corresponds to a structural phase transition from F-43m to Imma.

151 and decline are common in middle age, as are transitions from impairment to independence and back aga

152 t learn to forage effectively to survive the transition from parental provisioning to independent fee

153 verages our current understanding of disease transition from bacterial carriage to infection with the

154 first detailed picture of the nature of the transition from the metallic to insulating states of a 2

155 es between May and August, when transmission transitions from very low to intense.

156 mates reveals that the dominant noise source transitions from extrinsic to intrinsic as light intensi

157 The mechanisms that drive the transition from commensality to invasiveness in Staphylo

158 nally, C-GAP expression level influences the transition from reversible to irreversible cell shape ch

159 s human cancers, and it exhibits a tractable transition from its latent to its productive cycle in ce

160 solutions, which undergo a thermally induced transition from spheres to large compound micelles (LCM)

161 ndividual productivity and the timing of the transition from first- to last-author publications.

162 e disappearance of PtdIns3P that signals the transition from early to late phagosomes is accompanied

163 intermediate and late stages and during the transition from intermediate to late stage of OA in the

164 et of a secondary instability-related to the transition from HF to LF-occurs during the fast equilibr

165 which the core complex directs the necessary transitions from end pairing to ligation is not known.

166 our experiments support a model in which the transition from sedentary to light activity is associate

167 We demonstrated that the transition from full potency to lineage priming is preve

168 such as spatial connectivity, may lead to a transition from regional to local coexistence or it may

169 or (PMv) network during a gradual behavioral transition from full alertness to loss of consciousness

170 activity was preferentially involved in the transition from high to low gamma power that followed an

171 D19(-)IL-7R(+) progenitor compartment, which transitions from a myeloid to lymphoid program during on

172 is a strategy employed by KSHV to favor the transition from latency to lytic replication.IMPORTANCE

173 igate the translational landscape during the transition from normal homeostasis to malignancy.

174 Here, we show that TPMs acquired at the transition from benign nevus to malignant melanoma do no

175 of Prx1m for Leishmania parasites during the transition from insect to mammalian hosts.

176 24 hours or less, indicating the most rapid transition from colostrum to mature phase lactation yet

177 LPL was required for the transition from prealveolar macrophages to mature alveol

178 r data indicate that beta-TrCP regulates the transition from mitosis to meiosis in male germ cells by

179 Identifying key factors that regulate the transition from primary to metastatic cancer is a fundam

180 ate disease and the inability to predict the transition from mild to moderate disease.

181 ss measurements themselves could predict the transition from mild to moderate fibrosis with sufficien

182 tures and a mechanistic model of the folding transitions from native (N) to molten globule (MG) to ki

183 concentration-response relationship and the transition from oscillatory to more sustained and prolon

184 Transitions from SI to MP were not associated with weake

185 The transition from single-cell to multicellular behavior is

186 ts transmission is the symbiosis expected to transition from antagonism to mutualism.

187 cted temperature-induced morphological phase transition from the nanodot to nanoribbon regime.

188 (5 K) magneto-resistance (MR) data reveals a transition from positive to negative MR with increasing

189 her show that Sox2 is essential for cells to transition from the activated to neuronal progenitor sta

190 , strain-rate, and applied stress reveal the transition from Newtonian to non-Newtonian flow to be ub

191 by spontaneous symmetry breaking close to a transition from oscillatory to nonoscillatory dynamics.

192 ose related specifically to the evolutionary transition from blood feeding to obligate nonbiting.

193 Rifted margins mark a transition from continents to oceans and contain in thei

194 Overall, the data suggest that transitions from on- to off-states involve decreased mot

195 and mutations in alg-5 lead to a precocious transition from spermatogenesis to oogenesis.

196 of objective clinical criteria to guide the transition from intravenous to oral antibiotic therapy.

197 opening of the external gates as the protein transitioned from the inward to outward facing state.

198 Nutritional transition (from under- to overnutrition) among women of

199 The transition from asymptomatic to overt HFpEF is linked to

200 g frequency on pump detuning and observe the transition from period-1 to period-2 oscillation.

201 me, yet few data exist for the timing of the transition from acute to persistent critical illness.

202 resents an evolutionary link documenting the transition from chewing to piercing mouthparts in relati

203 The transition from molecular to plasmonic behaviour in meta

204 use of in situ solid-state NMR to probe the transition from intracrystalline catalysis to pore mouth

205 The timely transition from neural progenitor to post-mitotic neuron

206 The transition from prefusion to postfusion conformation of

207 rate was evaluated within each woman as she transitioned from pre- to postmenopause, defined by a bi

208 nia and identified widespread changes in the transition from prenatal to postnatal life.

209 2016) show that Lin28 controls the metabolic transition from naive to primed pluripotency by directly

210 we show that individual cells undergo abrupt transitions from a naive to primed pluripotent state.

211 dence interval 1.07, 1.47; P=0.005), whereas transition from public to private insurance was associat

212 nd CRT associated with edema recurrence upon transition from monthly to pro re nata (PRN) dosing were

213 It is therefore crucial to transition from reactive to proactive responses for thes

214 rationale for the observed disruption of the transition from distributive initiation to processive el

215 Fibrosis, driven by inflammation, marks the transition from benign to progressive stages of chronic

216 rucial molecular pathways that accompany the transition from quiescence to proliferation and differen

217 ngle, high-conductivity buffer expedites the transition from cell lysis to protein electrophoresis.

218 bium Josephson weak links that demonstrate a transition from ballistic to pseudo-diffusive like evane

219 ttributed to experiences) are central to the transition from anomalous experiences to psychotic sympt

220 (44%), continuous public coverage (27%), and transition from private to public coverage (11%).

221 confidence interval 1.19, 1.56; P<0.001) and transition from private to public insurance (hazard rati

222 In these analyses, transition from private to public insurance was associat

223 application for decision-making requires the transition from qualitative to quantitative AOP (qAOP).

224 e latter, the critical flexibility marks the transition from periodicity to quasi-periodicity in the

225 nanofibers are aligned parallel undergoing a transition from three to quasi-two dimension, light ampl

226 evelopment, neural stem cells (NSCs) undergo transitions from neuroepithelial cells to radial glial c

227 As the climate warms, a transition from winter snow to rain in high latitudes wi

228 The ongoing transition from rapid prototyping to rapid manufacturing

229 t affected by methylation changes during the transition from pre-receptive to receptive phase.

230 -104) and a low, but nonzero, probability of transition from disease progression to recovery (median

231 cortical and striatal function underlie the transition from novel actions to refined motor skills.

232 For suspended films, the transition from transmitter to reflector occurs when the

233 The molecular pathways that regulate the transition from renal progenitor to renal vesicle are no

234 t and recruited immune cells, and the phased transition from destructive to reparative inflammation.

235 Winter cereals require prolonged cold to transition from vegetative to reproductive development.

236 ciated with an alluvial floodplain ecosystem transitioning from agricultural production to restoratio

237 Additionally, analysis of the transition from ADP to rigor provides a structural ratio

238 eon with 3 additional surgeons progressively transitioning from open to robotic during the study peri

239 Cells transition from spread to rounded morphologies in divers

240 ion, but it promotes a hunger for salt and a transition from salt resistance to salt sensitivity.

241 t a change in the nature of the metamagnetic transition from first to second order-like at a tricriti

242 The transition from first- to second-generation MFC resulted

243 ptimises storage reserve mobilisation in the transition from seed to seedling via control of ERFVII a

244 ating system evolution, with the most common transition from outcrossing to self-fertilizing.

245 Such a trend represents a transition from long- to short-term memory processes whe

246 skeletal muscle of the rabbit occurs during transition from isometric contraction to shortening unde

247 The structure transition from sI to sII occurred during the methane-et

248 sulting in incommensurate layers, there is a transition from sticking to sliding with Aubry-type sign

249 examine defects in the in situ thermal phase transition from nematic to smectic A in hybrid-aligned l

250 The transition from C3 to so-called "proto-Kranz" anatomy re

251 semiclassical model and shown to be due to a transition from strong to soft recollisions with increas

252 lies the formation of crystals and the phase transition from liquid to solid.

253 The transition from proliferation to specification is fundam

254 the cargo is loaded into the SNP during heat-transition from rod-to-sphere.

255 , with inverse abundance dynamics during the transition from fall to spring.

256 ea level) across 12 mountains containing the transition from northern hardwood to spruce-fir forests.

257 -independent resistivity upturn with a clear transition from logarithmic- to square-root temperature

258 y dissipation by the defects and predict the transition from bouncing to sticking.

259 The mechanisms regulating the transition from single to streaming cell migration remai

260 Phosphate release gates a transition from weak to strong F-actin-binding states.

261 hysically discontinuous structure during the transition from infragranular to supragranular neuron pr

262 Transition from an asymptomatic to symptomatic state in

263 enborough (DvH) to collapse after repeatedly transitioning from sulfate respiration to syntrophic con

264 deamination of cytosine is a major source of transitions from C*G to T*A base pairs, which account fo

265 be an essential epigenetic regulator of the transition from progenitor cells to terminally different

266 ) and has been shown to be important for the transition from elongation to termination during transcr

267 The crystal structure of bulk SrTiO3(STO) transitions from cubic to tetragonal at around 105 K.

268 for the study of evolutionary traits in the transition from fishes to tetrapods.

269 al conformational changes that accompany the transition from each state to the next throughout the tr

270 However, little is known about how the transition from inflammatory signaling to the engagement

271 The transition from the autoinhibited to the active form of

272 and a pronounced free-energy barrier at the transition from the epidermis to the dermis underneath,

273 Gamete differentiation initiates the transition from the gametophyte to the sporophyte genera

274 at lower temperature that may be due to the transition from the HO to the LMAFM phase.

275 00 nm) regime, but scattered behavior in the transition from the nanocrystalline to the ultra-fine re

276 nd even a direct kinship relation across the transition from the Neolithic to the Bronze Age add to t

277 as material culture in central Europe at the transition from the Neolithic to the Bronze Age.

278 The transition from the off to the on state is triggered by

279 d separation within monomer units during the transition from the oligomer to the fibril form.

280 , one that appears to be associated with the transition from the PM to the HO phase and another one a

281 riton condensates that might be described as transition from the thermal to the quantum annealing reg

282 interact with the actin thin filament during transition from the weakly to the strongly bound state w

283 The transition from vegetative to the reproductive stage is

284 re combined, between the two song types when transitioning from one to the other, and/or (ii) singers

285 r the first time that T. cruzi epimastigotes transitioning from the exponential to the stationary pha

286 decreases the number of actin-binding heads transitioning from the weakly to the strongly bound stat

287 ations have calculated that the cTnC paralog transitions from the closed to the open state more readi

288 Strikingly, as the system transitions from the quantum to the classical regime, th

289 ations of increasing elevation is the abrupt transitions from forest to treeless alpine tundra.

290 Here we observed the rich kinetics of transitions from square lattices to triangular lattices

291 nnections contribute to speed-dependent gait transition from walk, to trot, and then to gallop and bo

292 including mice, demonstrate sequential gait transitions from walk to trot and to gallop and bound.

293 onlinear Schr odinger equation demonstrate a transition from single-pulse to two-soliton bound-states

294 Our data also reveal a sharp transition from folded dimer to unfolded monomer between

295 ations are stochastic, and therefore lead to transitions from stable to unstable community states.

296 Paleoclimate proxy data indicate that a transition from colder to warmer climate conditions is p

297 e workflow, supporting seamless quantitative transition from MS to WB.

298 We attribute these characteristics to a transition from strong to weak interaction regimes in a

299 l materials from damage by creating a smooth transition from strong to weak that dissipates large for

300 FACT can recognize and bind Z-DNA or DNA in transition from a B to Z form.