ライフサイエンスコーパス: general model

1 nt was associated with SCD risk (P=0.008 for general model).

2 b-models also are precisely predicted by the general model.

3 rate models are suggested as steps toward a general model.

4 tability estimates were lower using the more general model.

5 onsumer-resource models are derived from the general model.

6 simulations confirmed these findings for the general models.

7 rimental detail leads to the construction of general models.

8 azard ratios (HR) (95% CIs) were as follows: general model, 0.58 (.25-1.31); model with PS, 0.69 (.29

9 The general model accommodates data from acorn woodpeckers a

10 Notably, the general model achieved a better performance than existin

11 at rate curves and describe how to use it in general modeling activities and analysis.

12 minally associated with type 2 diabetes in a general model (additive P = 0.03, dominant P = 0.005) bu

13 Articulating these states into a general model allows for dissecting, comparing, and deri

14 t aspect of reserve design (MPA size) into a general model and determined their combined influence on

15 We describe these both in terms of general modelling and addressing the specific conditions

16 This general modeling approach is potentially applicable to o

17 However, there are only two general modeling approaches in conventional electronic s

18 this ecosystem, supporting the concept that general models are applicable to predict the behavior of

19 able to other locations (transferability) or general models are applicable to smaller areas (generali

20 Topaz-Denoise and pre-trained general models are now included in Topaz.

21 rivations of the analyses, carried out for a general model, are provided in an Appendix.

22 This paradigm may offer a general model as to how tissue-specific regulatory mecha

23 Here, we use a general model based on biochemical kinetics to quantify

24 trait variation and partitioning suggested a general model based on four interconnected findings.

25 Here we derive a general model, based on first principles of allometry an

26 We derive a general model, based on principles of biochemical kineti

27 t-output mapping for training stimuli, and a general model-based strategy that utilizes humans' defau

28 We also developed a general, model-based approach to gauge the effects of fa

29 The specific and general models both compared well with existing methods

30 ration effect could yet be predicted using a general model built on refined wheat (adjusted R2: 0.998

31 Here we develop a general model by combining memory effect and population-

32 We outline a general model by which corepressors and coactivators reg

33 These results suggest a general model by which differential adhesion can be util

34 ned with data from the martian meteorites, a general model can be constructed that constrains the his

35 There are currently two general models competing to explain the role of subjecti

36 sis of carbon-leaving group (C-LG) bonds, no general models connect structure to reactivity for heter

37 Three general models connect these patterns to anatomical evol

38 oaches have remained disconnected because no general models currently provide a means of directly com

39 We exhibit two examples of this general model describing assembly of dodecahedral and ic

40 A previous general model describing physical constraints on gamete

41 We present a general model describing the growth of layered materials

42 Despite these similarities, general models describing how plant defenses function in

43 teria or insecticides) performed better than general models developed on all data.

44 The resulting general model enables interpreting each phase of the dos

45 We examine the identifiability of a general model encompassing three such mechanisms: popula

46 These results suggest a general model explaining how ATP hydrolysis is coupled t

47 Based on these data, we propose a general model explaining how expression of the MMO opero

48 own has a negligible effect, demonstrating a general model finding that varying the expression levels

49 This Viewpoint outlines this general model, focusing on the specific example of Arabi

50 We specify this general model for 11 generic consumer strategies that gr

51 first set a stochastic equation system as a general model for a heterogeneous quorum sensing network

52 The data support the general model for ABC transporters in which the NBDs for

53 mechanism in striatal neurons and suggest a general model for achieving rapid posttranslational subu

54 id leukemia (AML) in mice is often used as a general model for AML.

55 e in APP regulation and may determine a more general model for amyloid generation as seen in AD.

56 In this paper we present a general model for an information management system that

57 me of Wynberg's reaction and provides a new, general model for asymmetric cinchona organocatalysis.

58 These results suggest a general model for auxin signalling in which the modulati

59 Our discoveries suggest a general model for bacterial pathogens in which mutations

60 We also propose a general model for birth-order-dependent neural specifica

61 Based on our results, we propose a general model for branching during maize inflorescence d

62 alleles of low frequency may serve as a more general model for complex genetic diseases, posing a sig

63 X-ray diffraction data support a general model for crustaceans in which tails associate t

64 Herein we develop a rigorous and general model for defect formation in the presence of st

65 refore suggest an alternative to the current general model for DNA unwinding by hexameric helicases.

66 s of nuclear organization, contributing to a general model for enhancer function that involves direct

67 sistance with measured values, and provide a general model for examining the diversity gill morpholog

68 sphate pools, and from DNA, and we suggest a general model for excluding purine base analogs from DNA

69 sm described in HIV-1 PR is proposed to be a general model for flap closing in retroviral aspartic pr

70 We present a general model for fluorescence quenching by hydrogen don

71 , genes, and gene expression, and provides a general model for gene evolution following whole-genome

72 Our findings allow us to formulate a general model for generation of periodic pattern in the

73 termediates are generated and may serve as a general model for highly processive travelling machines

74 lycan binding region of EBLs, and suggests a general model for how DBL domains evolve under dual sele

75 d an anti-ligase function in Emi1 suggests a general model for how E3 substrates evolve to become pse

76 Based on these findings, we propose a general model for how Hsp104 and related chaperones oper

77 This could serve as a general model for how signaling regulates postendocytic

78 nges in synaptic efficacy and may serve as a general model for how surface receptor number is establi

79 Our method is appropriate under a very general model for how the site influences the trait, inc

80 The conversion serves as a general model for integration of multiple pathway resour

81 s interactions with lipid micelles provide a general model for interactions between TSPs, membranes,

82 stitutive transcriptional activator may be a general model for its oncogenic conversion in myeloid le

83 onformational changes in KirBac1.1 provide a general model for ligand-induced Kir channel gating at t

84 We propose a general model for Ni(2+) recognition in which betaHis81

85 This study provides a general model for niche-induced fate determination in ad

86 These findings suggest a general model for oncogenic complicon formation.

87 Based on these findings, we propose a general model for oncogenic mutants of p85 and p110 in w

88 We suggest a general model for paramyxovirus fusion activation in whi

89 We suggest a general model for paramyxovirus fusion activation in whi

90 yeast RFC-PCNA complex, thereby presenting a general model for PCNA loading by RFC in archaea and euk

91 s drawn from disturbance ecology to create a general model for population dynamics in disturbance-pro

92 functions are extremely useful for forming a general model for predicting physical properties of comp

93 These findings suggest a general model for predicting the susceptibility of prote

94 of whether it is unique to humans or a more general model for primate vision.

95 se findings provide a structural basis and a general model for product specificity in PRMTs, which wi

96 e we establish and experimentally validate a general model for Rayleigh scattering in FMFs.

97 number of known targets, but also develops a general model for RBPs with limited or null known target

98 ate at different residues and also suggest a general model for regulation of PRMTs.

99 orded from the rodent hippocampus suggests a general model for remembering episodes.

100 These findings lead to a general model for Rho binding and translocation and esta

101 Here we develop a general model for shell growth based entirely on the loc

102 ses Igk germline transcription and provide a general model for STAT5-mediated epigenetic transcriptio

103 has recently established this organism as a general model for studying cytokinesis.

104 To provide a general model for studying the role of oligopeptide repe

105 om Bacteroides thetaiotaomicron and derive a general model for substrate translocation.

106 Beyond the AOB, this study presents a general model for synchronous infra-slow bursting in neu

107 The proposed mechanism may provide a general model for the antisickling effects of aldehyde c

108 ight-chain variable domains is proposed as a general model for the assembly of protein fibrils.

109 genetic relationships, leading to a revised general model for the biosynthesis of these virulence-co

110 production of IL-7 by thymic stroma may be a general model for the clinically observed adverse effect

111 Our results suggest a general model for the conformational switch in the cycli

112 regulation of CMG disassembly and provide a general model for the disassembly of ubiquitylated prote

113 train divergence and evolution, as well as a general model for the discovery of functional mutations

114 It may also suggest a general model for the evolutionary flexibility of conser

115 ly mammalian development and could provide a general model for the genomic response to acquisition of

116 CaM-Na(V)1.5 IQ motif complex can serve as a general model for the interaction between CaM and ion ch

117 ve been subject to intense investigation, no general model for the molecular basis of nonadditive gen

118 We propose a general model for the requirement of host RNA polymerase

119 We now propose a general model for the role of Aha1 in the Hsp90 ATPase c

120 for other mammalian OBP-ligand complexes, a general model for the role of OBPs in mammalian olfactio

121 ther DNA processing pathways, and proposes a general model for the role of RPA in protein-mediated ha

122 This requirement leads to a general model for the spreading and inheritance of silen

123 Our results provide a general model for the stepwise process leading to genome

124 )-DNA cleavable complex, we have developed a general model for the ternary drug-DNA-TOP1 cleavable co

125 tify four additional TTN genes and present a general model for the titan phenotype.

126 nd nociceptors expressing TRPM8, providing a general model for this form of cold-induced pain.

127 In the general model for transcription-coupled DNA repair, an R

128 We present a general model for understanding the stereochemical cours

129 We develop and test a general model for variation within and between species i

130 Finally, we describe a general model for VNTR mutations that encompasses insert

131 ain structures has allowed us to formulate a general model for why most L27 domains form an obligate

132 To test general models for membrane-protein folding and to ident

133 ndividuals in the same analysis and to allow general models for the crossover process to incorporate

134 We present general models for the relationship between enhanced fus

135 To overcome this limitation, we develop a general modeling framework to shed light on the relative

136 We present and analyse a general modelling framework for systems where breeders a

137 We shall discuss a more general modelling framework of interactions of structure

138 We provide a general modelling framework to jointly infer infection h

139 ell firing in the AcbSh is consistent with a general model from other pharmacological and electrophys

140 Then, defining a rather general model Hamiltonian for the donor material, we sho

141 A general model has been proposed for the fusion mechanism

142 Earlier general models have investigated when environmental pred

143 In this paper we provide evidence that a general model in the network science on opinion dynamics

144 ther membrane protein complexes has led to a general model in which a unique, ordered pathway is foll

145 We propose a general model in which conditional disorder-the partial

146 These data suggest a general model in which convergent maps use coincident ac

147 1 restriction in T cells, and they suggest a general model in which multiple APOBEC3 proteins functio

148 ucleic acids, a hypothesis consistent with a general model in which some modern biochemical systems r

149 ibition and open probability, supporting the general model in which the bi-lobe motion in ATD regulat

150 ses of both cell types can be described by a general model in which the outputs of a set of linear fi

151 ation in cellular extracts and in terms of a general model in which VHR may be a general MAP kinase p

152 For a general model incorporating the role of succession or pa

153 We develop a general model incorporating viral dynamics and pharmacok

154 We use a general model, incorporating biological components and d

155 A general model indicates a marrow cell that can continual

156 A quantitative and general model is derived for the interaction potential o

157 The general model is described and illustrated by examining

158 A general model is developed to characterize the effect of

159 On the basis of these results, a general model is proposed for the interfacial binding of

160 A general model is proposed whereby up to 10 levels of sig

161 This general model is tested in a matching task in which rewa

162 The general model is, typically, analytically intractable, b

163 Our simple, general model leads us to propose a principled method to

164 r the tether material after crossover, and a general modeling method for tether pulling experiments.

165 results with computational simulations using general model networks and anatomical brain networks, as

166 We present a general model of actin filament deformation and fragment

167 Here, we develop a general model of admixture that mechanistically accounts

168 etailed quantitative agreement with a recent general model of allosteric cooperativity that exhibits

169 Positioning "incentive hope" in a general model of behavioral control systems removes arti

170 on of the mature T-cell compartment and as a general model of binary lineage decisions, the underlyin

171 I then develop a very general model of cancer progression, which I use to expl

172 These results support a general model of chaperone-mediated protein quality cont

173 reserve therefore provides an empirical yet general model of cognitive aging and development.

174 Our results suggest a general model of cortical function, whereby horizontal c

175 The general model of covalently attaching a small protein as

176 Animal models have implicated a general model of crystal-induced inflammation involving

177 : a commonly used predator-prey model, and a general model of cyclic trophic interactions.

178 These results suggest a general model of DMPK regulation with two main regulator

179 In this paper we present a general model of drug release from a drug delivery devic

180 a step in the development of a parsimonious, general model of economic choice.

181 Here we derive a general model of ecosystem respiration based on the kine

182 However, we propose a general model of endemic stability that is applicable to

183 orage, and use these patterns to formulate a general model of energy allocation between growth, lipid

184 hese patterns we propose DEBlipid, a simple, general model of energy allocation that is closely relat

185 essions for the velocity and run length of a general model of finitely processive helicases, the two

186 s in tissue mechanical properties provides a general model of force buffering that serves to preserve

187 We use the framework of a general model of fractal-like distribution networks toge

188 t about by "globalization," application of a general model of freedom based on ecological-economic fa

189 -specificity of HpTx2 and point the way to a general model of gating modifier toxin interaction with

190 propose hierarchical Gaussian processes as a general model of gene expression time-series, with appli

191 While a general model of H2 activation has been proposed for [Fe

192 We developed a general model of heat flux to evaluate whether water req

193 These findings suggest a general model of how pH-dependent proteinaceous inhibito

194 Our observations lead to a general model of how substrates, such as ethanol, can re

195 nd at actively transcribed genes and offer a general model of how ubiquitin might regulate the activi

196 A transmission model that includes a general model of human mobility significantly improves p

197 rial dysfunction and cardiomyopathy and as a general model of inducible, reversible cardiomyopathy.

198 In this review, we discuss a general model of integration of environmental cues by Tr

199 eoretical analysis of a previously-developed general model of inter-trial error correction is used to

200 ap sizes and shapes in the ectoderm, using a general model of interstitial gap mechanics.

201 We use our quantitative results to propose a general model of long-range electrostatic screening in i

202 rovide experimental evidence to support this general model of memristive electrical switching in oxid

203 We find that a general model of morphological selectivity has a low pro

204 A general model of neural development is derived to fit 18

205 we extend this framework by linking it to a general model of parasite accumulation.

206 Here, we use a general model of periodic patterning to show that differ

207 these findings support the conclusion that a general model of permeability will require consideration

208 to colocalize in RPE, CE, and MDCK cells, a general model of polarized epithelia.

209 also point to a new, biologically important general model of precise and selective interaction betwe

210 These results indicate that a general model of protein evolution will emerge as more f

211 can be fabricated on silicon, and suggest a general model of quantum-state fabrication using other c

212 In this study, a general model of recombination in circular molecules is

213 Here we develop a general model of recurrent selective sweeps in a coalesc

214 We describe a general model of resistance development, including persi

215 nder anoxic conditions and also serving as a general model of saturated pyrimidine residues.

216 The general model of selective sweeps we describe goes some

217 To provide the experimental basis for a general model of short-term plasticity, we studied three

218 Here, we study a general model of spatially embedded networks with depend

219 Here, we introduce a general model of spurious association in structured popu

220 We describe here a general model of structural variation that encompasses b

221 r with previous data, our findings lead to a general model of substrate and inhibitor coupling to P-g

222 I construct a general model of the interactive feedbacks of host prefe

223 We describe here a general model of the kinetic mechanism of protein foldin

224 learned joint torque responses rather than a general model of the object interface forces.

225 Replication concepts are defined and a general model of the steps in DNA replication is present

226 These observations also led to a general model of the unfolding transition state structur

227 A general model of this process, the territorial-expansion

228 The main conclusion of the study is that a general model of vasomotion that predicts experimental d

229 We develop a general model of word formation and demonstrate the conn

230 ton acceptor or the tyrosine, in accord with general models of amino acid radicals.

231 Over 25 years of study have produced two general models of apoA-I structure in discoidal HDL comp

232 ld be a fruitful direction for building more general models of biodiversity response to climate chang

233 perates in time will be necessary to develop general models of cognition.

234 iminish and it became incorporated into more general models of higher dysfunction.

235 spectrum in a finite population for several general models of multiallelic selection.

236 Within the Thrive Collaborative, six general models of peer support were identified: communit

237 s age, many studies have claimed support for general models of range evolution in which the area occu

238 In general, modeling oil-recovery is a challenging problem

239 General models on the evolution of policing have focused

240 The general model organism database (GMOD) tool kit has prod

241 models of hourly PNC was limited, but that a general model performed acceptably in multiple areas whe

242 ng approaches, we are able to perform a more general model prediction that takes into account the sus

243 In general, model predictions can be improved through bette

244 The general model presented advances previous treatments, an

245 We end by considering a general model proposing that adult neurogenesis is not a

246 We demonstrate that our general model provides a host of specific insights, incl

247 Our findings provide an initial general model relating small molecule binding and sequen

248 We build an analytical and general model resulting from simplifications assuming sm

249 cts and tests whether the predictions of the general models still hold.

250 This general model suggests that the roles of nicotinic and m

251 , we analyze the analytical predictions of a general model suitable for describing the spatial biodiv

252 Nevertheless, a general model supposed a compromise between the best and

253 alga Ectocarpus has led to it emerging as a general model system for this group, but additional mode

254 s which are independent of normalization and general modeling techniques; these factors might include

255 However, a general model that accounts for the formation and evolut

256 putational work is remarkable and provides a general model that can be used for studying the interact

257 erized as part of an instantiation of a more general model that describes the interaction between und

258 functional theory calculations, we suggest a general model that enables prediction of the feasibility

259 evolution better than we do CAM, I propose a general model that explains and unites C(4) and CAM evol

260 onent analysis can be utilized to estimate a general model that includes the well-known Pritchard-Ste

261 ing force in gradient dynamics, we develop a general model that is capable of capturing both subtle a

262 ard, as a possible explanation, a simple and general model that relates these data to the steric hind

263 inding regions in the parameter space of the general model that results in a quasispecies only compos

264 Finally, we develop a general model that shows how these effects can be captur

265 We then developed a general model that shows these individual fitness reduct

266 s an alternative, this study proposes a more general model that uses detailed organism and tissue com

267 different environments - we achieved a more general model that well-predicted leaf age across forest

268 Two general models that are consistent with the biochemical

269 rate our knowledge, it is necessary to build general models that begin with an input image and predic

270 ween theory and data, we study a simple, but general, model that explicitly focuses on the dynamics o

271 In general, models that allow chimps to have a larger per-r

272 ecent studies question whether the classical general model (the Jeffress model) applies across specie

273 Under the conditions of this general model, the maximum expected correlation between

274 This approach results in a simple and general model to account for product accumulation in int

275 We have recently proposed a general model to account for these atypicalities in Baye

276 divergence, containing the foundations for a general model to anticipate and predict within-target-fa

277 We develop a general model to describe both loss of immunity in the a

278 ian viral communities, and provide a robust, general model to predict viral host range and guide path

279 Here, we present a general model to show that this type of interaction can

280 We apply this general model to study assembly of FtsZ protein, a basic

281 chanism described in this study represents a general model to understand the involvement of nonspecif

282 We attempt to test three possible general models to account for this behavior: 1) The Q(o)

283 ition of distinct island geodynamics permits general models to be developed and modified to account f

284 We then consider special cases of our general model under which we can examine the consequence

285 Thus, the general model unifies the four major models of reproduct

286 with alpha-quaternary centers, have led to a general model useful for the prediction of product selec

287 A general model was applied to discriminate high-quality n

288 A general model was developed to assist in the rational de

289 General model was not suited to distinguish PDO red wine

290 This general model was tested within a phylogenetically infor

291 Using a general model we predict the qualitative and quantitativ

292 The general model we present is able to denoise new datasets

293 Here we examine a general model where population growth can be induced or

294 ion of the transition density function for a general model where the effective population size, selec

295 ubiquitous in nature, our results support a general model whereby antagonistic interactions and natu

296 Our findings support a general model whereby DNA ligand binding with VirD4 and

297 This approach forms the basis for our general model, which predicts sites on drugs that are su

298 in two ways-by considering (analytically) a general model with a minimal number of assumptions and,

299 that was a thousand-fold larger than a more general model within which the first model was fully nes

300 less than or equal to the probability of the general model within which the special case is nested.