ライフサイエンスコーパス: rule for

1 We derived a prediction rule for 1-year ischemic stroke risk post-TIA, examining

2 parsimonious model and a clinical prediction rule for 10-year all-cause mortality.

3 SI-2 meets all of the criteria of Lipinski's rule for a drug-like molecule and has a half-life of 1 h

4 learning rule, we present an online learning rule for a recurrent neural network that achieves near-m

5 a subset of bacterial OSTs follow their own rules for acceptor-site specificity, thereby expanding t

6 New rules for access and benefit sharing (ABS) of genetic re

7 structure given the task of defining uniform rules for access to and distribution of health care, ben

8 h the circularly polarized optical selection rules for addressing individual valley excitons and trio

9 ign of ligands targeting RNA has established rules for affecting RNA targets and provided a potential

10 n inference to identify three key behavioral rules for aggregation: cluster-edge reversals, a density

11 a variety of locations follow a generalized rule: for all nerve pathway origins, the soma cluster ce

12 that redefine previous, non-evidence based "rules" for antibiotics.

13 In this review, five of the effective design rules for approaching LBG semiconducting polymers with h

14 te the efficacy of this 'Eighty Five Percent Rule' for artificial neural networks used in AI and biol

15 Our analysis provides design rules for artificial photosynthetic systems based on org

16 ssifications and structural analyses provide rules for assigning current and future human RBD-targeti

17 A prediction rule for asthma in preschool children might help to dete

18 4.1, Glt1, and Ca(2+) The data show that the rules for astrocyte engagement in a neuronal circuit are

19 a(2+)and glutamate indicators to explore the rules for astrocyte engagement in the corticostriatal ci

20 linear discriminant analysis, classification rules for authentic and paraffin adulterated beeswax sam

21 versions of instruments; and (e) setting the rules for authorship in advance.

22 al principles for AI, and derived evaluation rules for autonomous AI, grounded in bioethical principl

23 in a generative model, we investigate growth rules for axonal branching patterns in cat area 17, orig

24 and February 2013 (when predefined stopping rules for benefit were met) and outcome evaluations cont

25 r establishing and implementing other simple rules for biological systems.

26 'runaway transcription' creates alternative rules for both global RNA surveillance and translational

27 SC-like structures provide insight into the rules for building and maintaining the SC by offering an

28 what these structures can tell us about the rules for building the SC and the roles of the SC in mei

29 sed on our experiences, we present 10 simple rules for busy faculty who want to create similar progra

30 Consequently, progress in developing design rules for cancer nanomedicines has been slow, hindering

31 Our results unveiled physical rules for cargo transport and positioning in networks of

32 ed to derive three additional classification rules for case subjects and one for control subjects.

33 t, and recently on bacteria, have identified rules for cell size regulation in single cells, but in t

34 ISECT) to identify the heterogeneous binding rules for cell-type-specific TF occupancy and analyze th

35 normal cell function and delineate possible rules for cellular geometry maintenance in populations o

36 We obtained more detailed specificity rules for certain functions by identifying the chemical

37 The allocation rules for chain-ending kidneys and the characteristics a

38 Two classification rules for children with versus children without CRS gave

39 during evolution, and Hebbian-like learning rules for clusters where neurons increase their synchron

40 A quantum circuit rule for combining quantum interference effects in the c

41 A prediction rule for community-onset 3GC-R infection was validated i

42 y validate two previously derived prediction rules for community-onset (CO) and hospital-onset (HO) s

43 the first steps toward developing synthetic rules for complex two-dimensional covalent organic chemi

44 ents and simulations suggest a simple design rule for controlled shape change.

45 requiring the memorization of instructed S-R rules for correct performance.

46 In this paper, we outline 10 simple rules for creating biological network figures for commun

47 These findings provide design rules for creating chemically driven soft robotic sheets

48 Origami describes rules for creating folded structures from patterns on a

49 ding of toxicity and guides us toward design rules for creating safe nanomaterials.

50 )avidin self-assembly and the current design rules for creating synthetic mimics.

51 titude flights are therefore not the general rule for crossing deserts in migrant songbirds.

52 nd this large amount of new information, new rules for crystal growth need to be developed and tested

53 the inter-Landau-level transition selection rules for dark trions, manifested by a distinctively dif

54 We aimed to develop simple predictive rules for death in less than 60 min and test the accurac

55 Application of the suggested rule for deciding about the time point of treatment cess

56 temperature programs and instituted a set of rules for defining the separation of OC and EC to quanti

57 A recognition, largely owing to their simple rules for design.

58 late gene expression, but we lack predictive rules for designing effective gRNA target sites.

59 s improved understanding, we propose several rules for designing experiments for minimizing off-targe

60 ifying new Env-host cell receptor pairs, the rules for designing optimal Env libraries are still uncl

61 Our findings also implicate rules for designing stable small RNAs, such as siRNAs.

62 The rule of 5 is a simple rule for detecting retinal nerve fiber layer (RNFL) chan

63 itivity analyses revealed that modifying the rule for determining vulnerability increased the vulnera

64 In this paper, we give rules for determining the behavior of a large class of [

65 ent sorts of input, forms of processing, and rules for determining the output are appropriate under d

66 e segmentation methods which utilized ad hoc rules for different applications.

67 Our reanalysis of data on cultural rules for displaying emotion from 32 countries [n = 5,34

68 ITDP may provide a general synaptic learning rule for distinct forms of hippocampal-dependent memory

69 which RNAs conforming to the strict sequence rules for DNA.RNA triplex formation may participate in f

70 re experiments) were eliminated and when the rules for doing so had been defined.

71 t algorithm that properly addresses all SBGN rules for drawing PD maps, including placement of substr

72 The model identifies distinct sets of rules for each age group by using Boolean operators to d

73 We generated distinct sets of rules for each age group to capture the temporal differe

74 sis in accordance with defined fragmentation rules for each phospholipid (PL) class.

75 ings establish ganglionic eminence-dependent rules for early synaptic integration programs of distinc

76 ticular food web matrix properties as design rules for economically and biologically sustainable indu

77 Here we suggest design rules for effective molecules by considering their molec

78 vestigate single-guide RNA (sgRNA) targeting rules for effective transcriptional activation, to demon

79 Our results suggest design rules for efficient high-surface-area solar cells with n

80 ogether these properties define the temporal rules for efficient information transfer at DG-CA3 synap

81 dented opportunity to investigate the design rules for efficient nanoparticle occlusion within host i

82 However, robust design rules for efficient occlusion remain elusive.

83 These results serve as design rules for efficient photoswitchable DNA sequences tailor

84 We show that the majority of published "rules" for efficient sgRNA design do not effectively pre

85 The "14-day rule" for embryo research stipulates that experiments wi

86 und, we have identified new materials design rules for emerging sodium-ion systems that do not apply

87 ndent plasticity (STDP), a synaptic learning rule for encoding learning and memory, relies on relativ

88 e partially complementary, offering a design rule for enhancing delivery.

89 electronic-based discussion, following clear rules for establishing consensus and agreement/disagreem

90 organisms is the exception, rather than the rule, for eukaryotes.

91 Existing rules for fatigue life prediction, such as the linear cu

92 These findings describe general rules for feed-forward versus feedback inhibition and su

93 The rule for Feedback-based Online Local Learning Of Weights

94 atibilities in a rare exception to Haldane's rule for female sterility in field cricket sister specie

95 The development of design rules for flexizyme-catalyzed acylation should allow sca

96 , derived from the histograms, traffic-light rules for frequently observed, rare, and highly unlikely

97 for inhibitory neurons, suggesting different rules for functional excitatory-inhibitory interactions

98 Finally, we observe that there are general rules for functional molecular motors across the differe

99 nts of these materials yields general design rules for further improving horizontal orientation.

100 A pre-specified stopping rule for futility at interim analysis led the trial to b

101 In accordance with a prespecified stopping rule for futility of finding one drug to be superior or

102 ials (n = 36 per group), additional stopping rules for futility lead to the saving of resources of up

103 s a step toward establishing a set of design rules for future immunotherapies, materials that intrins

104 f the left propeller loop, which extends the rules for G-quadruplex folding.

105 bined with a suite of assumed physiological 'rules' for genera-specific bloom development.

106 ment specific enhancements, such as negation rules for general practitioners' entries and a regular e

107 ic tissue-specific genes, uncover regulatory rules for generating diverse gene expression patterns, a

108 Beginning with the superposition rule for genuine partially coherent sources, we derive s

109 and propose a new probabilistic analysis of rules for glass forming ability using rough set theory.

110 e aromaticity, combined with Huckel's 4n + 2 rule for ground-state aromaticity, to tailor new potenti

111 A futility rule for GVHD-free survival at day 56 was met at a plann

112 e results in the context of chemoinformatics rules for handling tautomerism.

113 DNA </= 2 x 10(5) IU/mL, the APASL stopping rule for HBeAg-negative CHB patients with proper off-the

114 The sensitivities of three clinical decision rules for head injuries in children were high when used

115 Graft allocation rules for heart transplantation are necessary because of

116 Four modes with different sets of rules for heuristic filtering of candidate formulas comi

117 nal/self-discharge mechanisms and the design rules for high performance.

118 erformance based on recent theory and design rules for high-definition (HD) IR imaging.

119 urthermore, this approach may reveal general rules for how circuit structure and neural coding within

120 This work helps define the rules for how different cortical areas interact in time

121 t guilds, suggesting that there may be basic rules for how sets of antagonists interact with resource

122 membrane proteins must be recovered, but the rules for how this multiple cargo selection is accomplis

123 Using these results, we postulated a folding rule for i-motif formation, analogous to (but different

124 guide future research by delineating several rules for identifying appropriate templates and molecula

125 Thus, our study provides rules for identifying cell-type-specific functional mamm

126 dy was the first to establish classification rules for identifying CRS in school-aged children, using

127 Further, they help define rules for identifying druggable targets in the transcrip

128 igators to train and evaluate classification rules for identifying objects related to processes like

129 We present design rules for IDPs possessing SLCs that phase separate into

130 Here we establish design rules for implementing this sequence-control in material

131 amics are poorly understood, rational design rules for improving activity remain unclear.

132 two dimensions, one can similarly define ice rules for in-plane Ising-like spins arranged on a kagome

133 tion to treat with a Peto-Haybittle stopping rule for (in)efficacy.

134 the system automatically generates low-level rules for independent climbing robots that guarantee pro

135 We found that the rules for induction of long-term and single-trial plasti

136 ceptors to control the efficacy and temporal rules for information transfer at DG-CA3 connections.

137 triage criteria prescribe specific transport rules for injured patients.

138 hermal properties might establish new design rules for intelligent labels.

139 proposed to develop simple and reproducible rules for interim PET reporting in lymphoma.

140 In this context, fundamental design rules for interlayers are revealed, which assist the cha

141 Reaction rules for intestinal degradation and human biotransforma

142 the need for developing individual agronomic rules for iodine biofortification of carrot for: (a) con

143 ructural design rules analogous to Pauling's rules for ionic crystallization.

144 lar mechanism of formation and establish key rules for its design and regulation.

145 Here, we derive such a rule for learning a near-optimal linear combination of D

146 A plausible synaptic plasticity rule for learning that balances weight configurations is

147 We have formulated four rules for licensing data for open drug discovery, which

148 In addition, design rules for light-regulated DNA logic gates were derived.

149 New CRISPR effectors and rules for locating optimum targets continue to be report

150 provides a powerful heterosynaptic learning rule for long-term gating of information flow through th

151 Thus, SB based matching rules for LT candidates might improve the survival of th

152 labeling experiments as a central filtering rule for maximizing phosphopeptide identification and qu

153 In color vision, the quantitative rules for mixing lights to make a target color are well

154 By contrast, the rules for mixing odorants to make a target odor remain e

155 4), consistent with the 4n electron counting rule for Mobius aromaticity.

156 ed that long-term persistence (>1 y) was the rule for most dsDNA viruses observed, suggesting that bo

157 ngle-gene effects are the exception, not the rule, for most diseases.

158 In this paper, we present the design rules for multiflavored particles and show that a single

159 s mechanisms of establishing and maintaining rules for multiple perceptual decision tasks.

160 Finally, we give simple dynamical rules for neural birth and death processes that might un

161 s and QDs, one that can provide clear design rules for new materials.

162 This provides design rules for next-generation materials to minimize losses r

163 e scientific community to develop consistent rules for nomenclature of uncultivated taxa in order to

164 sed on bulk absorbance spectra and selection rules for nonlinear hyperpolarizabilities.

165 solutes to such interfaces, providing design rules for novel interfacial chemistries.

166 By re-writing the rules for nucleic acid hybridization, Argonautes allow o

167 nt dimensionality regimes informs new design rules for optical devices where complex microstructures

168 illustrate its power by deriving non-obvious rules for optimal screen design.

169 Constantly, the rules for our sensory-to-motor mappings need to be adapt

170 We then combine such networks with learning rules for outputs or recurrent connections.

171 structural analysis define expanded pairing rules for over 200 mammalian miRNAs.

172 sport in active spinner materials and yields rules for particle manipulation at the microscale.

173 ial databases, we sought to develop stopping rules for patients destined to fail boceprevir-based com

174 With recent FDA rules for phasing-out antibiotics in animal production,

175 In this paper, we describe ten simple rules for planning, implementing, and evaluating teacher

176 /240 negative identifications) using defined rules for positive calls.

177 can be prevented by precisely balancing STDP rules for potentiation and depression; however, experime

178 hat represents a novel methodology to define rules for predicting gene function by examining the emer

179 s that are refining our understanding of the rules for predicting hadron structure from QCD.

180 reaction led to the development of powerful rules for predicting the regioselectivity of borylation,

181 stic acceptance of it to evaluate prediction rules for primary prevention of cardiovascular disease.

182 h, public health statistics, and eligibility rules for privileges or benefits.

183 results provide important and useful design rules for QD-based light harvesting applications using t

184 y, the breaking down of the dipole-selection rule for radiative transitions in isolated atoms.

185 vations and physical model establish general rules for raft partitioning of TMDs and support the cent

186 asic sequence features and employ elementary rules for ranking possible sgRNAs.

187 This lays ground rules for rational control of membrane proteins in nanot

188 subtle material issues of control and design rules for reconfigurable dipolar materials with building

189 marking reveals distinctive factor-specific rules for recruitment of these crucial transcription fac

190 We derive rules for retrieval motif recognition from key structura

191 sional RNA modeling and the discovery of new rules for RNA structure design.

192 ate how to implement a sequential monitoring rule for safety using a completed phase I trial that inc

193 The system generates candidate names using rules for scientific names and applies probabilistic mac

194 vailability of electronic media and parental rules for sedentary behaviours was self-reported by chil

195 is of the analysis, we propose the "OH-site" rule for seeing red and green.

196 Rules for selecting appropriate reactions to generate su

197 s transplanted bacterial enzyme, and provide rules for selecting Cas9 target sites distinct from and

198 ve inhibitors targeting these sites, but the rules for selective targeting of site 3 are less clear.

199 iews, peer interviews, scores using an "and" rule for self- and peer reports, and separate tests for

200 results, hence, provide an important design rule for self-assembled organic nanowires.

201 extrinsic plasticity (DEP) as a new synaptic rule for self-learning systems and apply it to a number

202 philicity, which resulted in a set of design rules for self-assembling sequences.

203 Taking advantage of the universal rules for self-assembly of complementary oligonucleotide

204 formly distributed over its surface, and the rules for self-replication are encoded into the specific

205 any have viewed microbes as following strict rules for shifting their metabolic activities when preva

206 orrhage score is a valid clinical prediction rule for short-term mortality in intracerebral hemorrhag

207 Our observations allowed for deducing a rule for SLC6 family members: a hydrophobic residue (Tyr

208 alized to the compliance with another set of rules for social interactions, namely the fairness norm,

209 We identify rules for specific targeting of transcriptional represso

210 rm competition, (ii) use the same allocation rules for sperm and seminal fluid, and (iii) experience

211 structure-activity relationships and design rules for spherical nucleic acids (SNAs) functioning as

212 re to nicotine during adolescence alters the rules for spike timing-dependent plasticity in prefronta

213 dividual release sites also revealed general rules for spontaneous and evoked release, and indicate t

214 d Protection Agency (EPA) proposed a revised rule for "Standards of Performance for Greenhouse Gas Em

215 ve ability of the CHA(2)DS(2)VASc prediction rule for stroke and death in a nonanticoagulated populat

216 y new metabolites and development of general rules for structural determination of tagged metabolites

217 lometric method harnessing normative scaling rules for subcortical size and shape in humans, which we

218 of complex pictures and to combine them in a rule for subsequent choices.

219 g those that adhere to the more common N-end rule for substrate recognition.

220 Then, we applied five rules for successful multiparty negotiations: 1) levelin

221 terim analysis met the prespecified stopping rule for superiority.

222 The study met futility rules for survival after enrolling 146 of 259 patients.

223 ientation by tensile stress offers a general rule for symmetric cell division in plants.

224 arning, and unravel a distinct architectural rule for synapse formation in the adult brain.

225 The learning rule for synapses that target hidden neurons is modulate

226 Furthermore, the learning rule for synapses that target visible neurons can be mat

227 urones in the inferior olive implement novel rules for synaptic integration and suggest new principle

228 are robustly expressed, suggesting different rules for synaptic plasticity across these regions.

229 c events in a wide temporal window, and that rules for synaptic plasticity in human neocortex are rev

230 learning and suggest major revisions to the rules for synaptic plasticity in the cerebellum.

231 eins and how this information informs design rules for synthetic systems.

232 slational blockage and have relaxed matching rules for takeoff/landing sites.

233 emical and genetic analyses to delineate the rules for TAM receptor-ligand engagement and find that t

234 To date, no clinical prediction rule for TB risk exists for use as a guide during contac

235 Our results argue against a simple rule for the arrangement of inhibitory inputs supplied b

236 According to the SLICC rule for the classification of SLE, the patient must sat

237 at allows the formulation of a new empirical rule for the direct assignment of the C2 stereochemistry

238 ndings confirm predictions of a magic number rule for the family of {Pdx } macrocycles.

239 n described by the 70% proportional recovery rule for the Fugl-Meyer motor upper extremity (FM-UE) sc

240 owest triplet states as compared to Huckel's rule for the ground state (S0).

241 which provides a hitherto unexpected design rule for the incorporation of nanoparticles within cryst

242 The 1,2,3-Rule for the initial management of MK was conceived by V

243 interactions between networks play a crucial rule for the outcome of evolutionary games taking place

244 iously explained by an economical clustering rule for the probability of functional connectivity betw

245 We unambiguously demonstrated the solvation rule for the solid-electrolyte interphase (SEI) enabler

246 Moreover, since the classical 12/23 rule for the V(D)J recombination fails to explain the V(

247 The "1, 2, 3 Rule" for the initial management of MK was conceived by

248 Nevertheless, adoption of uniform rules for the allocation of kidneys would reduce the var

249 This review seeks to set the basic ground rules for the analysis of different initiation pathways

250 s area requires the identification of design rules for the chromatin system.

251 icomponent droplets is still incomplete, and rules for the coexistence of condensed phases are lackin

252 Using (modifiable) filter rules for the commonly used methoximated-trimethylsilyla

253 To define rules for the design of Cas13d guide RNAs (gRNAs), we co

254 AD co-oligomer and therefore to draw general rules for the design of PDI-based dyads and triads with

255 the mathematics of tessellations, we derive rules for the design of single CMPs that self-assemble i

256 ds have been condensed into a set of general rules for the design of thermostable CHA circuits with h

257 We established rules for the design of tight tubulin-SLD assemblies and

258 Thus, this work provides new design rules for the development of thermodynamically efficient

259 Furthermore, we formulate propensity rules for the distribution of products, and we develop a

260 meso-scale behavior is translated into logic rules for the dynamics.

261 e segment, providing simple geometric design rules for the fabrication of complex 3D structures.

262 Identifying rules for the heterogeneity of modern biodiversity-the h

263 This suggests that cocaine resets the rules for the induction of synaptic long-term plasticity

264 These data reveal clear rules for the inhibitory function of CTLA-4 on regulator

265 colleagues, has developed DSSs and decision rules for the management of diseases in a variety of cro

266 mmunity ecology, as a way of finding general rules for the mechanisms driving changes in community st

267 sualize the resulting networks, defining the rules for the molecular interactions typically requires

268 ved of these CTCF interactions have specific rules for the orientation of the paired CTCF sites, impl

269 We present a set of rules for the prediction of folding properties and the s

270 Here, we describe unanticipated timing rules for the production of long-term potentiation (LTP)

271 Common rules for the strategies employed by both hosts and viru

272 of these experiments provide a set of ground rules for the successful engineering of hr-PKS and PKS-N

273 By identifying four critical rules for the superlattice configuration we lay the foun

274 ent literature regarding clinical prediction rules for the use of cranial computed tomography (CT) in

275 rto overlooked dependence on (or 'propensity rule' for) the magnetic quantum number m of the molecule

276 lgi proteins contain K(x)Kxx motifs, but the rules for their recognition are unclear.

277 membrane voltage sensors, and provide design rules for their structure and composition.

278 lack of a clear physical picture and design rule for this device has led to numerous invalid fabrica

279 are few organizational principles or guiding rules for this highly hysteretic, dissipative material.

280 ditis elegans, uncovering a conserved set of rules for this protein modification and identifying subs

281 e an important exception to temperature-size rules for three reasons: (i) we use many more species th

282 d Drug Administration (FDA) issued the final rule for title 21 of Code of Federal Regulations part 21

283 An early stopping rule for toxicity was included, defined as grade 3 to 4

284 cal structural descriptors to derive general rules for trapping molecules in high-energy conformation

285 progressed, and use of a CVR-based decision rule for treatment in which patients with CVR impairment

286 Although important rules for Treg selection have been established, there is

287 This review also describes the rules for TRM generation and the properties that disting

288 ulate the energy landscape, we obtain design rules for tuning the actuation behavior.

289 a range of force-fields), we derived robust rules for urea unfolding that are valid at the proteome

290 ant next step would be to develop prediction rules for use in clinical practice, so that older person

291 r, neither a specific calculation method nor rules for use of retention factors are defined.

292 and Drug Administration recently issued new rules for using ceftiofur in food animals in part becaus

293 Scoring threshold rules for visual assessment and management of pigmented

294 This is discussed in terms of the general rules for Voronoi patterns (Dirichlet tessellations) in

295 nucleobase pairs follow standard rules for Watson-Crick base pairing but have rearranged

296 ediction error, with an approximate Bayesian rule, for which beliefs in latent states are proportiona

297 e resulting model combines a Rescorla-Wagner rule, for which updates to associations are proportional

298 Movement rules for which departure from patches depended on resou

299 Here, we discuss 10 specific rules for writing software papers, covering some of the

300 lectric material, cannot be a general design rule for ZT enhancement and a detailed transport study i