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 that summarizes our observations and suggest rules for a designer's tool box.

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

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

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

9 To investigate more intensively the grammar rules for active regulatory sequence, we made libraries

10 An adaptive treatment strategy (ATS) is a rule for adapting a treatment plan to a patient's histor

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

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

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

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

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

16 4.1, Glt1, and Ca(2+) The data show that the rules for astrocyte engagement in a neuronal circuit are

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

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

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

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

21 preted with an expanded version of Polanyi's Rules for bimolecular reactions, and three trends are ev

22 ne isomers that follow the isolated pentagon rule for C(82), the cage stability changes markedly betw

23 The simple rules for calculating flux in multistep mechanisms are d

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

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

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

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

28 The prediction rule for children aged 2 years and older (normal mental

29 In the validation population, the prediction rule for children younger than 2 years (normal mental st

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

31 erived and validated age-specific prediction rules for ciTBI (death from traumatic brain injury, neur

32 aining set generated a decision-making tree (rule) for classifying voxels as malignant or benign, whi

33 ead injury can now be guided by a prediction rule for clinically important traumatic brain injury.

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

35 n of the fishery ecosystem, and that the 10% rule for collapse should not be interpreted out of conte

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

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

38 anotechnology in many ways, the base-pairing rules for constructing nanoparticles are different.

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

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

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

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

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

44 bursting in a manner analogous to the timing rule for cue-reward learning paradigms in behaving anima

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

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

47 in version 1.2.1 or higher and the stopping rule for declaring a change early is available in versio

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

49 rospective study was to develop a prediction rule for delirium in a cardiac surgery cohort and to val

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

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

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

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

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

55 as small as 60 nm and provide simple design rules for determining the conditions under which nanocha

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

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

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

59 g to fundamentally distinct Hebbian learning rules for distal versus proximal synapses.

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

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

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

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

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

65 rmore, instead of a few master combinatorial rules for each stress condition, many rules were discove

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

67 planned to enroll 128 patients, but stopping rules for early termination were met.

68 Rules for early termination within each disease type wer

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

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

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

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

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

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

75 an be understood in terms of the Wade-Mingos rules for electron counting, suggesting that it may be a

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

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

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

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

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

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

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

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

84 s confirmed that the mode symmetry selection rules for FCS are the same as for Raman scattering and t

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

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

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

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

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

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

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

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

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

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

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

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

97 al regulators in sperm, suggesting different rules for H3K36me3 in the germline and soma.

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

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

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

101 or the first time, one can establish general rules for heavy metal binding to Cys-rich sites in desig

102 DB), we have deciphered and rationalized new rules for helix-helix interfaces of a common protein-fol

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

104 hat only the latter followed the established rules for hierarchy of translation termination.

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

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

107 lpha-binding sequences; we also identify new rules for HNF4alpha DNA binding.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

123 les are enumerated, which specify the ground rules for industry-sponsored research.

124 cuits with intrinsically active neurons have rules for information transfer and storage that distingu

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

126 triage criteria prescribe specific transport rules for injured patients.

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

128 icipants were randomized based on a stopping rule for intervention efficacy.

129 Reaction rules for intestinal degradation and human biotransforma

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

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

132 I derive expanded versions of Hamilton's rule for kith and kind selection, generalizing Hamilton'

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

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

135 ly confined optical fields, the conventional rules for light-matter interactions need to be re-examin

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

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

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

139 agment library, the bioisostere library, the rules for metabolic stability, the toxicophore library,

140 rly experimental evidence, a set of "binding rules" for miRNAs has been described.

141 trand-break-repair events, each with its own rules for mismatch repair of heteroduplexes.

142 Chargaff's second parity rules for mononucleotides and oligonucleotides (CIImono

143 ytically testing the accuracy of the product rule for more than five loci has hitherto remained an op

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

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

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

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

148 e quantification of species variation around rules for network design.

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

150 Further analyses reveal three rules for NLS recognition by Kap beta 2: NLSs are struct

151 nominal mass), and eliminating the "nitrogen rule" for nominal mass determination of number of nitrog

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

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

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

155 However, the rules for orderly recruitment of presynaptic components

156 tive explanatory power, the functions of and rules for organizing maps and their plasticity are not w

157 The prespecified stopping rule for OS has not yet been reached.

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

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

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

161 rophobic surface area; (iii) a well-defined "rule" for packing of stable cores exists, but this rule

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

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

164 tudy was to determine quantitative injection rules for pediatric PET allowing clinical implementation

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

166 /240 negative identifications) using defined rules for positive calls.

167 New risk factors and a prediction rule for postthoracotomy atrial fibrillation are discuss

168 nder which underlying spike-timing-dependent rules for potentiation and depression can be separated f

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

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

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

172 ts establishes the general utility of the RS rules for predicting retinocollicular topography, and de

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

174 However, there are few rules for predicting the relative stability of folded co

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

176 Here we examine the cellular scaling rules for primate brains and show that brain size increa

177 Under National Institutes of Health rules for protection of human subjects, studies based on

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

179 el-to-fluid melting temperatures (T(m)), the rules for raft formation in membranes are not completely

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

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

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

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

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

185 derived and validated a clinical prediction rule for recurrent CDI that is simple, reliable, and acc

186 This study aimed to develop a prediction rule for recurrent CDI using the above derivation cohort

187 The simple combinatorial rules for regulation of the sloppy-paired-1 (slp1) gene

188 gly, these results raise questions about the rules for renal filtration, given that these large molec

189 We derive rules for retrieval motif recognition from key structura

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

191 (N)2 reaction in solution, as the "Solvation Rule for S(N)2 Reactions" predicts.

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

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

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

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

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

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

204 derivative that does not obey the classical "rules" for shape and functional group placement that are

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

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

207 We identify rules for specific targeting of transcriptional represso

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

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

210 ese findings, coupled with other established rules for SR proteins, provide a theoretical framework t

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

212 We also introduce a rule for stopping early when there is strong evidence fo

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

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

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

216 on between SH3BP2 and Tankyrase and describe rules for substrate recognition by this poly(ADP-ribose)

217 wo coupled leaves and derive the Gibbs Phase Rule for such a system.

218 terim analysis met the prespecified stopping rule for superiority.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

233 ing techniques (2) development of a decision rule for the constructed FLN to optimize functional anno

234 n the form of an activity-dependent learning rule for the development of retinocollicular projections

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

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

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

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

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

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

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

242 the foundation toward defining the molecular rules for the ARO/CYC cyclization specificity, whose rat

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

244 This study suggests a set of design rules for the clinical translation of targeted nanoparti

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

246 The rules for the conserved reaction of alphabeta T cell rec

247 Delineation of these and other rules for the control of protein oligomer assembly by ch

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

249 is essential for the development of general rules for the design of peptoids with discrete and novel

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

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

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

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

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

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

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

257 d use, but are far from providing predictive rules for the function of regulatory DNA.

258 The argumentation rules for the gene expression example are available from

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

260 homoallylic system dissociated according to rules for the homoallylic system, with an additional fra

261 Here we examine spatial organizational rules for the human brain oscillatory activity as measur

262 we analyze current data to distill a set of rules for the induction and maintenance of central memor

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

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

268 The rules for the palindrome-dependent pathway of gene ampli

269 Thus, like humans, the cognitive rules for the perception of auditory groups amidst multi

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

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

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

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

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

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

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

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

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

279 ully defined system in accord with the 12/23 rule for this process.

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

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

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

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

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

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

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

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

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

289 otility and is therefore an exception to the rule for two-component signaling.

290 Rules for unlikely missed cleavage and nontryptic proteo

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

292 A triage decision rule for use in an epidemic was developed using only tho

293 A "shortcut" of the advanced Mosher rule for use in assigning stereocenters in molecules wit

294 cent study introduces a validated prediction rule for use in mild CHI, to limit the number of CT scan

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

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

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

298 Scoring threshold rules for visual assessment and management of pigmented

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

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