ライフサイエンスコーパス: transition

1 transition and (ii) deprotonates in K --> M transition.

2 duces reversion of epithelial to mesenchymal transition.

3 le with a magnetic field-induced topological transition.

4 ells undergoing endothelial-to-hematopoietic transition.

5 ope and accompanied by a semiconductor-metal transition.

6 mmunication, academic, nonmedical tasks, and transition.

7 ortant to inhibit endothelial-to-mesenchymal transition.

8 ere described as necessary for this M1 to M2 transition.

9 led channel, plays a fundamental role in the transition.

10 (MA = CH3NH3(+)) with no apparent structural transition.

11 tes is consistent with a model of sequential transition.

12 locking development at the morula-blastocyst transition.

13 servation of hallmarks of a reversible phase transition.

14 xample of a (zero temperature) quantum phase transition.

15 ally realize a mixed-order equilibrium phase transition.

16 st-order thermodynamics nature of this phase transition.

17 that experience superconductor-to-insulator transition.

18 recruitment) represents a major life-history transition.

19 emergent functionalities due to topological transitions.

20 nide signal and assign underlying electronic transitions.

21 ion across a variety of mammalian cell state transitions.

22 nd- and sequence-context-dependent GC --> AT transitions.

23 for medical setbacks; and 5) disruptive care transitions.

24 rapid cell cycles preceding the midblastula transition, a defined timing program was present that pr

25 o broaden our understanding of the Neolithic transition across Europe, we analyzed eight ancient geno

26 S) cell differentiation, uncovering discrete transitions across nine cell states.

27 skull shape and form across the agricultural transition, although these changes have proved difficult

28 undergoes a hydrogen bond change in D --> K transition and (ii) deprotonates in K --> M transition.

29 anomaly is a field-induced metamagnetic-like transition and affects both magnetisation and magnetostr

30 Fbeta from inducing epithelial-myofibroblast transition and cell migration but did not prevent fiber

31 The molecular basis for the O1 --> O2 transition and how ChR2 modulates selectivity between st

32 which may promote endothelial-to-mesenchymal transition and proliferation of mesenchymal cells.

33 ed at the level of epithelial-to-mesenchymal transition and the ERK1/2 signaling pathway inversely af

34 d B-lymphopoiesis at the pro-B to pre-B-cell transition and, contrary to their proposed dominant-nega

35 The methods each use two infrared absorption transitions and a resonant Raman transition to create a

36 Multiexcitonic transitions and emission of several photons per excitati

37 PP TC development across juvenile, transition, and adult leaves correlated positively with

38 quids, Berezinskii-Kosterlitz-Thouless phase transition, and classical magnetism, among the many syst

39 The early-night peak in p20, limiting G1/S transition, and its phase angle with the expression of c

40 e related across the nematic-smectic A phase transition, and presents new possibilities for controlle

41 ater mass properties at the Plio-Pleistocene transition, as Circumpolar Deep Water (CDW) became the c

42 agnitude faster than competing single-photon transitions, as opposed to being as much as 8-10 orders

43 suggest a molecular mechanism underlying the transition between a better-known repressive function of

44 On heating, this compound exhibits a spin transition between a LS ground state and an ordered HS-L

45 The simulations revealed a distinct transition between energetically sustainable and unsusta

46 t is possible to drive the cuprates across a transition between Mott and Slater physics, where a spin

47 epeat DNA act as hot spots to facilitate the transition between the two configurations, which may giv

48 sis-free within this range, which includes a transition between two structural phases.

49 ete extraction of the monacolins and minimal transitions between the monacolins during analysis.

50 The rates of the transitions between the recognition sites can be control

51 nterdependent mechanisms that underpin rapid transitions between transcriptional states, and elucidat

52 adipogenic through an epithelial-mesenchymal transition both in vitro and in vivo.

53 -specific manner during the oocyte-to-embryo transition by activating transcription, altering protein

54 We further showed the utility of this transition by designing smart, cell-penetrating polymers

55 -up triggers Chinmo/Imp to Syncrip/Broad/E93 transition by inducing expression of the Ecdysone recept

56 d-gap emission exceeds that of the excitonic transition by orders of magnitude.

57 We argue that such a transition can be described in mathematical terms as a s

58 orted by theory, show how the spin crossover transition can be manipulated reversibly around room tem

59 This RNA-mediated reentrant phase transition can drive the formation of dynamic droplet su

60 children detected a heterozygous c.206A-->T transition, causing an E69V missense mutation.

61 ecifying genes, and the opportunity for host transition could interact to promote the emergence of ho

62 Approaching the transition, DeltaPsi and ROS increased, and secretory gr

63 In the dyad, the electronic transition dipole moment of the electron donor perylene

64 egions in Eurasia, demonstrating that such a transition does not necessarily limit the genetic and li

65 ivity but also had the highest proportion in transition, either to abundance or rarity, thus offering

66 c functions including epithelial-mesenchymal transition (EMT) and cancer stem cell (CSC) acquisitions

67 ate and induces an epithelial-to-mesenchymal transition (EMT) by driving expression of the master EMT

68 gnaling during the epithelial to mesenchymal transition (EMT) from NMP to mesodermal progenitor.

69 Reversing epithelial-to-mesenchymal transition (EMT) in cancer cells has been widely conside

70 cells (CSCs) markers, epithelial-mesenchymal transition (EMT) inducers and basal-enriched molecules,

71 rentiation, and an epithelial to mesenchymal transition (EMT) transcriptional program.

72 role in promoting epithelial-to-mesenchymal transition (EMT), invasiveness and metastasis.

73 ng the involvement of epithelial-mesenchymal transition (EMT).

74 f genes related to epithelial-to-mesenchymal transition (EMT).

75 s caused by the 1000 K Mott metal-insulator transition, for which the thermal conductance counter-in

76 RS) method to monitor the onset of fat phase transition (freezing/melting) in human abdominal adipose

77 trols whose IQ is correlated with the neural transition frequency, IQ scores of individuals with ASD

78 al preferences of a model peptide during the transition from a hydrated environment (charged nanodrop

79 sential for alpha cell maturation during the transition from a milk-based diet to a chow-based diet a

80 lmitic, stearic or eicosanoic acids caused a transition from a one-step to two-step process.

81 its a negative differential resistance (NDR) transition from a steady flow to an immobile state.

82 le real-time microscopy in solution, shows a transition from an early stage of uniform Ag(0) incorpor

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

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

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

86 of the molecular mechanisms accompanying the transition from desired drug effects to adverse events f

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

88 n X-ray diffraction, we reveal a polymorphic transition from face-centred-cubic (fcc) structure to he

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

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

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

92 ian Ocean-Southern Pacific region, marking a transition from lower-than-average rates before 1990 tow

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

94 One of these magnificent examples is the transition from non-avian dinosaurs to birds that has cr

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

96 The transition from the last ice age to the present-day inte

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

98 ultistage process naturally leads to pattern transitions from actin vortices over stars into asters.

99 RKIP transitions from inhibiting Raf-1 to inhibiting G-protei

100 g multiband emission associated with optical transitions from the conduction band to lower E- and upp

101 l of the environment, in the form of a state transition function and reward function, can be converte

102 ZO-1 is critical for GJ channel closure and transitioning GJ channels for endocytosis.

103 mperature, T C < T < T*, where a first-order transition has been previously predicted.

104 ch are associated with the forbidden optical transitions, have been observed.

105 he adjusted hazard ratios (HRs) for 3 health transitions (healthy to dead, healthy to disabled, and d

106 nding the microscopic mechanism of the phase transitions, highlighting the importance of cooperative

107 al properties during the high-to-low-density transition in amorphous ice at 1 bar.

108 neural maps, which we link to a known phase transition in an Ising-like model from statistical mecha

109 pathways for the closed-open conformational transition in both directions by computing trajectories

110 has been lost to space, contributing to the transition in climate from an early, warm, wet environme

111 Facility to check whether the O- to C-state transition in fully activated fibers of fast skeletal mu

112 ration, invasion, and epithelial-mesenchymal transition in human prostate cancer cell lines, and stab

113 lastic moduli associated with a polyamorphic transition in La32Ce32Al16Ni5Cu15 bulk metallic glass an

114 nd investigate the dynamics across the phase transition in large arrays of atoms.

115 for neuronal migration, and suggest that the transition in mitotic dynamics can be studied in organoi

116 ion and thereby controls the mitosis-meiosis transition in mouse male germ cells.

117 upregulation, and a retrograde developmental transition in PDA metastasis.

118 ves of corn (Zea mays L.), we show that this transition in pHapo conveys functionality by (i) adjusti

119 tatic cancer, undergo epithelial to amoeboid transition in physiological environments, such as organo

120 A transition in the dominant dissipation pathways occurs a

121 n and ROS levels associated with mesenchymal transition in these cells.

122 The insulator-to-metal phase transition in vanadium dioxide (VO2) is a canonical exam

123 olymers undergo a reversible coil-to-globule transition in water after which the chains collapse and

124 created an injectable delivery platform that transitioned in <5min from a liquid at room temperature

125 ic sex determination facilitating land-water transitions in amniotes.

126 te the nature of the magnetic structures and transitions in monoclinic Co3TeO6.

127 the discovery of sequence/structure/function transitions in other enzyme superfamilies.

128 olyhedral distortions at symmetry-disallowed transitions in perovskites that may evidence underlying

129 how features of criticality known from phase transitions in physical systems.

130 ere, we present direct measurements of phase transitions in single bilayers of 1,2-dimyristoyl-sn-gly

131 Such events drive important transitions in social systems (e.g., banking collapses)

132 med RNA sequencing over these spatiotemporal transitions in the AGM region and supportive OP9 cell li

133 The structure is a transition intermediate where loop 83-89 closes to engag

134 Likewise, the transition into a burst/pause pattern results from combi

135 Some are making the transition into early-phase patient trials, but the lack

136 FN-gamma(+), adhere to CFB, and induce their transition into myofibroblasts.

137 ion intermediate populations and accelerated transition into SP cells.

138 This dynamical component slows down after transition into the low-density form at 130 K, but remai

139 Within this model, we observe phase transitions into spatially ordered states that break var

140 s the two-state transition is a composite of transitions involving at least nine unique species: thre

141 mobility distributions reveals the two-state transition is a composite of transitions involving at le

142 This approach revealed that the metastatic transition is accompanied by massive and recurrent alter

143 This transition is accompanied by widespread redistribution o

144 has arisen and to test whether this dietary transition is associated with higher species numbers in

145 The juvenile-to-adult transition is delayed, and proximal distal-patterning is

146 Such a pressure induced transition is known for covalent liquids, but has not be

147 and currently only one mid-larval molecular transition is known: Chinmo/Imp/Lin-28+ neuroblasts tran

148 sis indicates that mesenchymal-to-epithelial transition is requisite to initiate SMCs reprogramming i

149 terface, we confirm that the charge transfer transition is strongly aligned orthogonal to the heteroj

150 t the bract axis but, after the reproductive transition, it is antagonized by the MADS box transcript

151 lectron microscopy, and found a 10 nm thick transition layer composed of amorphous phase and nanocry

152 This discovery of the stem II structural transition leads to a model wherein DDX1 can act as an R

153 The NAO/AO phase transition leads to a rapidly strengthened Siberian High

154 The transition length scale, Lt, separating these two motion

155 onducting catalyst carrier and the supported transition metal active phase represents an elite strate

156 represents the first step towards a general transition metal catalysed synthesis of tetraarylmethane

157 Diverse late transition metal catalysts convert terminal or internal

158 . coordination/organometallic main group and transition metal chemistry, catalysis, medicinal chemist

159 This protocol describes the synthesis of two transition metal complexes, [Ir{dF(CF3)2ppy}2(bpy)]PF6 (

160 VSe2 is a transition metal dichaclogenide which has a charge- dens

161 Controllable growth of highly crystalline transition metal dichalcogenide (TMD) patterns with regu

162 Two-dimensional transition metal dichalcogenides (2D TMDs) have gained g

163 Electrons in monolayer transition metal dichalcogenides are characterized by va

164 he structural phases in 2D materials such as transition metal dichalcogenides are correlated with ele

165 ons can be isolated in line defects of other transition metal dichalcogenides, which may enable quant

166 wo-dimensional materials such as graphene or transition metal dichalcogenides.

167 Combining transition metal ion FRET, patch-clamp fluorometry, and

168 phase responses, coagulative activities, and transition metal ion sequestration, highlighting that th

169 y, but more recently, strategies that forego transition metal ions for p-block elements have emerged.

170 cent advances of nucleic acid-functionalized transition metal nanosheets in biosensing applications.

171 in a broad class of systems, including other transition metal oxides or sensitizers.

172 , and that uranium can thus mimic elementary transition metal reactivity, which may lead to the disco

173 We report an unprecedented transition metal-free coupling of indoles with aryl hali

174 y available substrates, short reaction time, transition metal-free, and gram-scale synthesis are the

175 given the propensity for sulfides to poison transition-metal catalysts.

176 cientific challenge to access Earth-abundant transition-metal complexes with long-lived charge-transf

177 sfer ((2)LMCT) state that is rarely seen for transition-metal complexes.

178 Transition-metal dichalcogenides (TMDs) are renowned for

179 The emergence of transition-metal dichalcogenides (TMDs) as atomically th

180 y of 3-alkynyl-3-alkyl/aryl 2-oxindole under transition-metal free condition.

181 e electrochemistry and outgassing of lithium transition-metal oxides (TMOs) has been largely overlook

182 More recently, an emerging paradigm of transition-metal signaling, where dynamic changes in tra

183 s area has been achieved with pincer-ligated transition-metal-based catalysts; this and related chemi

184 nt bifunctional electrocatalysts based on 3D transition-metal-based materials for oxygen evolution re

185 Additionally, many transition-metal-catalyzed C-H bond additions to polariz

186 ncorporated in complex molecules via various transition-metal-catalyzed carbonylation reactions.

187 s a facile remote C-H HAT step, with that of transition-metal-catalyzed chemistry (selective beta-hyd

188 diamine (bbeda) is a landmark methodology in transition-metal-catalyzed cycloisomerization.

189 The transition-metal-free reaction proceeds in a regio- and

190 s of AMZ and bacteria showed that Al, P, and transition metals (Fe, Cu, Mn, and Zn) were exchanged du

191 i.e., Ti, Zr, and Hf) or V (i.e., Nb and Ta) transition metals are substituted into zeolite *BEA, the

192 ing cathode materials, Na(Li1/3 M2/3 )O2 (M: transition metals featuring stabilized M(4+) ), for furt

193 Transition metals have been researched extensively in th

194 In an area traditionally dominated by transition metals, these results outline an approach for

195 are inherently challenging to activate using transition metals; however, ring-strain release can prov

196 Materials and Methods A state-transition microsimulation model of osteoporosis for pos

197 layer, but are negligible when magnetization transitions occur in Fe.

198 that activate mTOR and enable the metabolic transition of activated T cells.

199 val, migration and epithelial-to-mesenchymal transition of cancer cells.

200 hydrophobic environment for the colorimetric transition of nanoblends.

201 tory response mechanism, as indicated by the transition of NF-kappaB from its inactive to active stat

202 on to observe crystal structure and chemical transition of perovskites.

203 Transition of populations from rural to urban living cau

204 irst time, experimentally revealed the phase transition of ThC from B1 to P4/nmm at pressure of 58 G

205 he atoms, one can experimentally study phase transitions of open quantum systems.

206 t surface interactions induce conformational transitions of the monomer, which facilitate interaction

207 trostatic-doping control of structural phase transition opens up new possibilities for developing pha

208 marrow lineages, endothelial-to-mesenchymal transition, or blood.

209 and numerical simulation, we show that these transitions originate from the presence of barriers to p

210 The LCST phase transition originates from the interaction between water

211 hat dominates folding kinetics, known as the transition path time.

212 that both exhibit critical scaling near the transition point.

213 splicing, are highly dynamic during cellular transitions, preserve reading frame, and reveal intricac

214 Furthermore, intact G1/S transition (Rb-positive and low-molecular-weight isoform

215 cteristic of twitching motility comprise the transition region between different types of observed cr

216 ased expression of epithelial-to-mesenchymal transition-related genes.

217 al ions affect the HNH domain conformational transition remains elusive.

218 Analysis of brain transcriptomes during the transition reveals that corazonin, a neuropeptide homolo

219 To transition seamlessly between environments, we next esta

220 be used to favour some, and suppress other, transitions so that completion of a mechanical cycle in

221 l remains H-bonding to the peroxo OCu in the transition state (TS) and transfers the H(+) after the b

222 reactions proceed via a highly asynchronous transition state allowing easier bond formation between

223 eventually formed can the protein reach the transition state and continue folding.

224 y of Au-catalysts to the Bergman cyclization transition state as one of the key components of the lar

225 ion of the anhydride-methanol complex in the transition state as the factor leading to stereoselectiv

226 of binding that is indeed reflective of the transition state at the CARM1 active site.

227 he drive to minimize torsional strain in the transition state being coupled with assistance from hydr

228 governed by transient species, including the transition state for activated bimolecular reactions.

229 opic mass in F159Y PNP causes more efficient transition state formation.

230 are thus preorganized closer to the assumed transition state in these glycosylation reactions.

231 The predicted DFT transition state model is also in agreement with the exp

232 rine bond formation proceeds via a concerted transition state rather than a discrete Meisenheimer int

233 toluene and the N-oxyl aromatic rings in the transition state structures.

234 icle reviews the fundamentals of variational transition state theory (VTST), its recent theoretical d

235 3,3] sigmatropic shift where the pericyclic "transition state" becomes the most stable species on the

236 Diels-Alder reactions via a single ambimodal transition state, and a retro-Claisen rearrangement.

237 umber of weak interactions are formed at the transition state, including nonnative interactions, and

238 ceed in a concerted fashion through a cyclic transition state-are among the most powerful synthetic t

239 equilibrium geometry similar to the neutral transition state.

240 it has proven valuable to prepare and probe transition-state dynamics by the photodetachment of anio

241 en the putative product-determining isomeric transition states (DeltaDeltaE(double dagger)) in both t

242 Distortion-interaction analyses of the transition structures for deprotonation predicted using

243 vity exclusively to monosolvated-dimer-based transition structures.

244 blue color change upon the wetting-dewetting transition, suggesting that hydration-induced microscopi

245 curred during the vegetative-to-reproductive transition, suggesting that is most active and key for B

246 first-order field-induced metamagnetic phase transitions (T N = 58 K) and high spontaneous polarizati

247 net, we achieve unprecedented control of the transition temperature (between ferromagnetic and parama

248 ilized in any material that exhibits a glass-transition temperature (T g ) and a rubbery plateau.

249 The glass transition temperature (Tg) for all of the powders signi

250 mains disappear above a distinct miscibility transition temperature (Tmix) and reappear below Tmix, o

251 percooled liquids stop flowing below a glass transition temperature [Formula: see text] or whether mo

252 Annealing at the glass transition temperature at ambient pressure reverses stru

253 and shows a concentration-dependent, tunable transition temperature in aqueous solution.

254 hanges little with cooling towards the glass transition temperature, Tg.

255 pseudogaped metal above the superconducting transition temperature.

256 c states such as anomalous and possibly high-transition-temperature (Tc) superconductivity.

257 We developed a method to estimate glass transition temperatures based on the molar mass and mole

258 f linking polyamorphism with a liquid-liquid transition that could take place in the no-man's land, t

259 haclogenide which has a charge- density wave transition that has been well studied.

260 The results highlight a charge transfer transition that leads to changes in the viologen structu

261 forces will inhibit or drive the topological transitions that either refine or deform a tissue.

262 presses the oncogenic epithelial-mesencyhmal transition, thereby acting as a tumor suppressor.

263 A transition to a 24/7 in-house intensivist care model was

264 ls, arising from a loss in entropy as chains transition to a conformationally restricted bridged stat

265 istent with the proposition that naive cells transition to a distinct formative phase of pluripotency

266 claims of the record pressure nor the phase transition to a metallic state are supported by data and

267 Journal of Clinical Investigation marks the transition to a new editorial team from Johns Hopkins Un

268 Here we show that GSCs can reversibly transition to a slow-cycling, persistent state in respon

269 , RHEED oscillations and AFM data indicate a transition to a step-flow growth mode.

270 bitor, accelerates a subsequent VSDIV gating transition to accelerate entry into the slow inactivated

271 e response in preparation for the successful transition to air-breathing at birth.

272 For a seamless transition to alternative targeted agents, patients prog

273 organs of a deceased relative, or support a transition to an "opt-out" policy.

274 -to-cell differences in their probability to transition to another committed state.

275 sexual dimorphism observed in a model of the transition to chronic pain, hyperalgesic priming.

276 absorption transitions and a resonant Raman transition to create a coherent output beam, but they di

277 veal that they undergo an irreversible phase transition to cylindrical domains under the electric fie

278 relevant CeA neuroadaptions that promote the transition to dependence.

279 calcineurin, PKCbeta1, and p38 regulates the transition to differentiation.

280 at co-activation of Myc drives the immediate transition to highly proliferative and invasive adenocar

281 ved regulatory mechanisms evolved during the transition to multicellularity to control fundamental ce

282 ion is known: Chinmo/Imp/Lin-28+ neuroblasts transition to Syncrip+ neuroblasts.

283 ior to metamorphosis, in preparation for the transition to the adult form, in which the AP axis conve

284 the lateral hypothalamus, which promote the transition to wakefulness from non-rapid eye movement (N

285 n recent years mitochondrial DNA (mtDNA) has transitioned to greater prominence across diverse areas

286 ion of this fibrotic stroma, upon activation transitioning to a myofibroblast-like, high matrix secre

287 t generalists, and almost exclusively so for transitions to eusociality.

288 ntation this acclimation may support further transitions to sponge dominated reefs in the future.

289 stance to anoikis, epithelial-to-mesenchymal transition, tumor cell dormancy and escape from immune s

290 ssing on the pressure-driven insulator-metal transition using a combination of first-principles densi

291 Tailoring structural phase transitions using alloying is a novel idea with implicat

292 On the basis of energetic analysis, the main transition was identified as the breaking of van der Waa

293 We determine that the frequency of the transition, which is driven by two photons from a laser

294 The urgency of the transition will depend largely on the country-specific p

295 ntaneous Raman microscopy probes vibrational transitions with much narrower resonances (peak width of

296 , we report the existence of a sharp genomic transition zone below the photic zone, where bacterial a

297 xplants from the buccal mucosa (BM), HP, and transition zone of the lower lip (TZ) after six-day cult

298 of progression of Tgfbr2-deficient invasive transition zone squamous cell carcinoma.

299 hat silicate melt above and below the mantle transition zone, and atop the core-mantle boundary could

300 terrestrial environments and in the inherent transition zones between them.