ライフサイエンスコーパス: invariant

1 makes the speed of synaptic depression rate-invariant.

2 their activity is otherwise behavioral state invariant.

3 t dependence on the value of the topological invariant.

4 ly distinguished with any single topological invariant.

5 only class-insensitive but also translation-invariant.

6 test battery; this relationship was also age invariant.

7 ies of Berry curvature and topological Chern invariants(1,2).

8 atching that occurred between pairs remained invariant across activity type, indicating that this mea

9 context (relative coding), rather than being invariant across contexts (absolute coding).

10 l voice perception contains certain elements invariant across cultures/languages, while others are mo

11 llowing cold exposure, and expression shifts invariant among populations under high temperatures.

12 while critical thermal maximum (CT(MAX)) was invariant among populations.

13 4-bp stem at the base of the CEH are nearly invariant among Saccharomyces species, our results with

14 regulating six design parameters, each scale-invariant and achievable at the colloidal scale.

15 early embryonic cell lineages are considered invariant and are conserved between distantly related sp

16 ies are instead coded by the coactivation of invariant and context-independent engrams.

17 from two perspectives, relying on viewpoint-invariant and self-referenced representations.

18 etry class AI, which refers to time-reversal-invariant and spinless systems with no special spatial s

19 ociation studies, there has not been a model-invariant and test-independent tool that allows for both

20 al performance when accounting for both time-invariant and time-variant confounders (loneliness: coef

21 of the disturbing geopotential, the gravity invariants and their specific ratio, the strike angles a

22 eatures are model- and parameter-free, frame-invariant, and robust to measurement errors and can be c

23 These models and our procedures to define invariants are generalizable to higher coordination numb

24 Our results indicate that the invariant aspartate of the J-domain perturbs a conserved

25 We then define topological invariant associated with Floquet bands, and show that t

26 monstrate the abrupt change of a topological invariant at a certain point during this transition, cla

27 een a bulb glomerulus and piriform neuron is invariant at one.

28 , that are characterized by topological Hopf invariant, attract an intense attention in the diverse a

29 al approach to arbitrarily shape propagation-invariant beams by smart beam design based on caustics.

30 methods, and demonstrate various propagation-invariant beams experimentally, ranging from simple geom

31 of the -N(CH(3))(3)(+)-modified catalyst are invariant between pH 0 and 7.

32 and a cryptic stochasticity in an otherwise invariant C. elegans cell lineage.

33 this, we investigated cytokinesis during the invariant Caenorhabditis elegans embryonic divisions and

34 ited to associate to each vortex loop a knot invariant called the Alexander polynomial whose degree c

35 itioning the acyl-CoA thioester bond near an invariant catalytic histidine residue.

36 et to a complete set of tailored propagation-invariant caustics with intensities concentrated around

37 eterodimer noncovalently associated with the invariant CD3 dimers CD3egamma, CD3edelta, and CD3zetaze

38 odimer in noncovalent association with three invariant CD3 dimers.

39 es (Hippocampus) featured a highly divergent invariant chain (CD74).

40 The MHC class II invariant chain (Ii) has been used as an adjuvant to enh

41 activating expression of the p41 isoform of invariant chain CD74, which inhibits viral entry by bloc

42 ne protease essential for degradation of the invariant chain CD74.

43 coexpressed with surface class II-associated invariant chain peptides (CLIP) in human EBV-positive an

44 ic immune enhancer (truncated shark class II invariant chain) fused to the nonstructural (NS) protein

45 an upregulation of surface HLA-DR and CD74 (invariant chain), whereas CLIP was slightly but signific

46 Our study reveals that cell type-invariant chromatin association of Zfp281 provides an in

47 Whereas the invariant class shows a considerable absence of specific

48 two-step VT, incomplete VT, and temperature-invariant {Co(III)-cat-cat-Co(III)} states are observed.

49 aded coding, as in the neocortex, or a truly invariant code, in which the response-eliciting stimuli

50 memories is given by a combination of mostly invariant coding in the MTL with a representation of sen

51 stigated whether the AIP also contributes to invariant coding of OMAs across different visual formats

52 archy has distinct ranking and the resultant invariant combinations of dominant/secondary mutations y

53 a temporal segmentation to inherently scale-invariant, critical dynamics.

54 ondrial inactivity, reverts the oxidation of invariant Cys residues in FNIP1 and allows CUL2(FEM1B) t

55 rical [d(p1, p2) = d(p2, p1)] and complement-invariant [d(p1, p2) = d(1 - p2, 1 - p1)].

56 Level-invariant decoding of sound lateralization also becomes

57 n of annotated images to train a robust view-invariant deep neural network.

58 ural-network based SI classifier named scale-invariant deep neural-network classifier (SINC).

59 s and yet are characterized by a topological invariant defined in the bulk.

60 orrespondence between a non-zero topological invariant defined on the spectrum of the dynamic matrix

61 ials require the identification of quantized invariants describing the bulk quadrupole order.

62 gue that object responses remain stable, or 'invariant', despite changes in viewing conditions that c

63 ll trends in antidepressant use and all time-invariant differences across locations.

64 interval [CI] 1.3-2.4) controlling for time-invariant differences and secular trends.

65 -fold (95% CI 1.3, 2.4) controlling for time-invariant differences and secular trends.

66 static mechanism, allowing cells to maintain invariant diffusion across a 20 degrees C temperature ra

67 The model combines the temporally-invariant distribution of the scattered pressure field a

68 ic and mitotic blastomeres and displaying an invariant division pattern.

69 mall peptide SELF-1, which is composed of an invariant domain and a hypervariable C terminus, as a ke

70 rted a 2-kb DNA sequence underlying a tissue-invariant domain boundary-containing a CTCF-binding site

71 esultant phylogenetic tree topology is scale-invariant due to a singularity arising from large niche

72 as shorter recombination lifetimes and lower/invariant efficiencies, the serendipitous effect of D(2)

73 features of motor behavior (e.g., kinematic invariants, effort), the present study explored and quan

74 , during the 1992-1998 cholera epidemic, the invariant epidemic clone co-existed alongside highly div

75 ry visual cortex (V1), increasing in a scale invariant fashion with eccentricity.

76 curve, 0.83 +/- 0.08) one trained with time-invariant features (0.79 +/- 0.07; p < 0.05) and a rando

77 time-varying features to a model using time-invariant features and to models based on two prior publ

78 ysis were used to extract independent, scale-invariant features of torso shape from 3D scans of 43 ma

79 T cells expressing invariant gammadelta antigen receptors (gammadelta T cel

80 In the mouse thymus, invariant gammadelta T cells are generated at well-defin

81 programming and age-dependent generation of invariant gammadelta T cells occur in humans is not know

82 nerates, in an HSPC/Lin28b-dependent manner, invariant gammadelta T cells with programmed effector fu

83 Because this response window is rate-invariant, GluA3 extends the range of presynaptic firing

84 , and pubic hair, and discover body location-invariant GVP markers to distinguish individuals.

85 Six invariant H and C residues and W503 are essential for vi

86 It is characterized by two invariant histidine residues that play a critical role i

87 e EAs, the EX possesses a hybrid topological invariant (HTI), which consists of distinct winding numb

88 ates can always arise due to the topological invariant (i.e., all closed loops entail the same topolo

89 ing revealed a highly similar, largely state-invariant (i.e., intrinsic) spatial component across cog

90 ial case exists in which the action is scale invariant if it satisfies the following two constraints:

91 unique substrate specificity of ScCdc14 was invariant in homologs from eight diverse species of dika

92 ice are tightly linked to running speed, was invariant in rTg4510 mice during locomotion.

93 to understand whether the neural code stays invariant in the face of significant internal input modu

94 This conservation is SO(3) invariant in the relevant symmetry plane in real space p

95 g factor is that most animals are ordinarily invariant in their asymmetry, except when manipulated or

96 against external perturbations, topological invariants in physical systems are increasingly being co

97 Manipulating the topological invariants in these materials would allow the developmen

98 gion of a songbird, these patterns reflected invariant information about a learned stimulus relations

99 However, genomes are not invariant information stores but are purposefully altere

100 S. cerevisiae mitotic spindle and primes the invariant inheritance of the old spindle pole body (SPB,

101 c excitatory neuron classes and three region-invariant inhibitory neuron classes.

102 odel with uniform spatial pooling from scale invariant inputs.

103 This relatively invariant isotopic signature contrasts with that of the

104 degeneracies characterized by a topological invariant known as the Chern number (C).

105 Evolution experiments under invariant laboratory conditions typically show a higher

106 change in the bulk non-Hermitian topological invariant leads to a change of topological edge-mode loc

107 entification with Neural networks for Domain-invariant LEearning) was validated using data of four an

108 rmat of representation but on a higher, view-invariant level of abstraction.

109 iloring of the maximum lobe of a propagation-invariant light field and promises an increase in depth

110 In particular, propagation-invariant light fields such as Bessel, Airy, or Mathieu

111 e Seifert surface and hence knot topological invariants like the Alexander polynomial.

112 vidual lineages for the reconstruction of an invariant lineage tree.

113 cannot be combined to reconstruct a species-invariant lineage tree.

114 tomes to their exact position in C. elegans' invariant lineage.

115 interindividual spread, and mutation of the invariant lysine (K170) results in stability issues and

116 ture and in chickens, we determined that the invariant lysine 170 (K170) of MDV CHPK is required for

117 e-inactivating alanine substitutions for the invariant lysine in subdomain II or the aspartate in the

118 Previously seen as invariant machines with the same composition of componen

119 + T, NK, TCR-gammadelta, Mucosal associated invariant (MAIT), and NKT cells as well as monocytes, ma

120 edom depend on constraint density in a scale-invariant manner.

121 uces incoming and outgoing statistical Gibbs invariant measures.

122 erature parameter in the corresponding Gibbs invariant measures.

123 medial prefrontal node that utilizes a task-invariant mechanism for computing relative subjective va

124 on method aims to find a group of relatively invariant microbiome species across samples and conditio

125 cortical magnification, suggesting a nearly invariant modular organization throughout human V1.

126 d glycosylation site (N66) in addition to an invariant N32 encoded by all chimpanzee CD4 alleles.

127 Invariant natural killer (iNKT) cells are among the firs

128 by subsets of innate-like T cells, including invariant natural killer T (iNKT) and gammadelta-T cells

129 Innate T cells, including invariant natural killer T (iNKT) and mucosal-associated

130 n-4 (IL-4) is produced by a unique subset of invariant natural killer T (iNKT) cells (NKT2) in the th

131 Invariant natural killer T (iNKT) cells acquire effector

132 Human invariant natural killer T (iNKT) cells are a rare innat

133 Invariant natural killer T (iNKT) cells are innate-like

134 Invariant natural killer T (iNKT) cells are potent immun

135 Semi-invariant natural killer T (iNKT) cells are self-reactiv

136 We investigated the hypothesis that invariant natural killer T (iNKT) cells contribute to in

137 Invariant natural killer T (iNKT) cells have been tested

138 CD1d-restricted invariant natural killer T (iNKT) cells represent a hete

139 Invariant natural killer T (iNKT) cells serve as early r

140 , we profiled >10,000 differentiating thymic invariant natural killer T (iNKT) cells using single-cel

141 sident lymphocytes, including lipid-reactive invariant natural killer T (iNKT) cells.

142 Valpha24-invariant natural killer T (NKT) cells have shown potent

143 , we demonstrate that the cross-talk between invariant natural killer T cells (iNKT) and CD8(+) T cel

144 mily of receptors promote the progression of invariant natural killer T cells through the thymic matu

145 The scale-invariant nature of avalanches suggests that the brain i

146 they fail to demonstrate the existence of an invariant neural code.

147 tructure and show that this measure captures invariant neural representations tied to the learned rel

148 Surprisingly, call-type invariant neurons were found in both primary and seconda

149 meostasis in the CD4+ Th cell life cycle and invariant NK (iNK) T cell development and CD8+ T cell ma

150 mice has been attributed to a deficiency in invariant NK T (iNKT) cells.

151 was reduced in mice born by CS, whereas the invariant NKT (iNKT) cell subset was increased compared

152 esent the only livestock with an established invariant NKT (iNKT) cell-CD1d system.

153 Invariant NKT (iNKT) cells are an innate-like population

154 Invariant NKT (iNKT) cells are attractive therapeutic ta

155 Invariant NKT (iNKT) cells are innate lipid-reactive T c

156 Invariant NKT (iNKT) cells provide rapid innate T cell r

157 Activation of invariant NKT (iNKT) cells with glycolipid antigen drove

158 Mycobacterium-reactive natural killer (NK), invariant NKT (iNKT), mucosal-associated invariant T (MA

159 acterized by reduced intrahepatic numbers of invariant NKT and CD4(+) T cells that express tumor necr

160 and IL-22 production correlated with reduced invariant NKT cell numbers as well as lower IL-23 levels

161 ent and effector functions of T1D-protective invariant NKT cells.

162 ations of high-contrast images, relevant for invariant object recognition and considered a challenge

163 onset activity reflected threat probability, invariant of fear output, while ramping activity reflect

164 Here we measure three topological invariants of a quantum Hall material-photonic Landau le

165 e total free energy and stresses in terms of invariants of shear and area deformation.

166 ty functions (PDFs) between second and third invariants of the velocity gradient tensor (i.e. Q and R

167 The statistical behaviours of the invariants of the velocity gradient tensor and flow topo

168 The behaviours of second and third invariants of the velocity gradient tensor suggest that

169 Although we found no fully invariant OMA-selective neuron, we discovered a populati

170 o stabilization, we adopt a novel brightness-invariant optical flow algorithm that helps us reduce er

171 tries; however, to determine the topological invariant or charge in these chiral crystals, it is esse

172 en two gapped states changes either the Z(2) invariant or the locally stable valley Chern number.

173 e binding site for TFIID and is surprisingly invariant over a wide range of promoter strength.

174 In both species, preferred rhythms remained invariant over extended ranges of tempos, indicating nat

175 we find that surface soil moisture is scale invariant over regimes extending from a satellite footpr

176 erge with previous observations of spatially invariant patterns of FC derived from extremely slow and

177 which infants' gaze patterns exhibited scale invariant patterns of nested variability, an organizatio

178 To account for the possibly time-invariant physical couplings within the signaling networ

179 NNs with other ideas such as permutationally invariant polynomials or sums of environment-dependent a

180 erval (SCRI) design, which controls for time-invariant potential confounders.

181 network-based architecture to produce domain invariant predictions, and furthermore integrated a hidd

182 ersions indicative of nontrivial topological invariants present in the magnetic phase.

183 such structures often exhibit similar scale-invariant properties(2-9).

184 avior, and move-step fluctuations with scale invariant properties.

185 olycomb-related complex 2 (PRC2) through the invariant proteins RBBP4 and RBBP7.

186 he germline-encoded VDJ segments to generate invariant/public cytomegalovirus-reactive CDR3 sequences

187 which are unique one-dimensional propagation-invariant pulsed optical beams.

188 ale-aware parameterization schemes for scale invariant quantities, when a model has sufficient resolu

189 Our results suggest that to explain invariant recognition of objects by humans, neural netwo

190 ymmetry of tumor spheroids to derive a scale-invariant relationship between spheroid contractility an

191 rizing neural responses that is sensitive to invariant relationships that are critical for the percep

192 Multiplexed with this value-invariant representation of the task, we also found a re

193 First, an intensity-invariant representation of wind direction is computed b

194 ferent images from the same face into a view-invariant representation that can be used for recognitio

195 tion of different views into a unified, view-invariant representation.

196 ential of applied topology for understanding invariant representations in neural populations.SIGNIFIC

197 f cells: those encoding highly selective and invariant representations of abstract concepts, and memo

198 These invariant representations were found during tasks withou

199 than familiar faces, which have more robust, invariant representations.

200 mportant intermediate step in computing view-invariant representations.

201 y as an intermediate step in generating view-invariant representations.SIGNIFICANCE STATEMENT The rec

202 Mutations of these invariant residues impair B3GNT2 activity in cell assays

203 nces of UDA have eight out of nine typically invariant residues that bind to the N and C termini of b

204 ssense variants in KAT5 that affect normally invariant residues, with one at the chromodomain (p.Arg5

205 ing that previous model simulations assuming invariant resistance may have underestimated the impacts

206 However, even in the face of invariant selection, the drift barrier defined by the ge

207 polysomal ribosome fractions, we detected an invariant set of 72 of 79 core RPs, RACK1 and 2 of the 8

208 ing endogenous network (CCEN) composed of an invariant set of microRNAs over all the stages and stage

209 rial input function exhibited an essentially invariant shape across all animals and time points and c

210 e features as well as the scale and rotation invariant shape features are extracted, and a dynamic pr

211 We call an analysis method 'scale-invariant' (SI) if it gives the same result under differ

212 lectively constitute a prominent and largely invariant signature across acute and chronic infections.

213 n performance should be at least partly size invariant, since changes only in scale do not affect an

214 ponse onset, transient temporal profile, and invariant spectral properties.

215 We propose that the slower and rate-invariant speed of depression allows an initial response

216 Pb/(204)Pb ratios (15.5-15.6) and relatively invariant Sr, Nd, and Hf isotopes, the data suggest that

217 isms at monocular, depth-selective and depth-invariant stages of the visual hierarchy.

218 To test this hypothesis, sounds with invariant statistics were presented to measure human spa

219 r population coactivity that is sensitive to invariant stimulus structure and show that this measure

220 ores), and catalytic activity suggest nearly invariant structure and function for aluminosilicate zeo

221 ied topology is a promising tool to discover invariant structure in large datasets.

222 For the new ASs, we observe largely invariant substrate specificity that would facilitate th

223 ediated endocytosis involving the parasite's invariant surface glycoprotein 75 (ISG75), followed by t

224 transition in two-dimensional time-reversal invariant systems with spin-orbit coupling, thus serving

225 Mucosa-associated invariant T (MAIT) cell loss in chronic HIV-1 infection

226 reased responses of blood mucosal associated invariant T (MAIT) cells against in vitro stimulation wi

227 In human blood, mucosal-associated invariant T (MAIT) cells are abundant T cells that recog

228 Mucosal-associated invariant T (MAIT) cells are activated by microbial ribo

229 Mucosa-associated invariant T (MAIT) cells are an innate-like T cell subse

230 Mucosal-associated invariant T (MAIT) cells are an innate-like T cell subse

231 Mucosal-associated invariant T (MAIT) cells are important for immune respon

232 Mucosal-associated invariant T (MAIT) cells are innate T lymphocytes activa

233 Mucosa-associated invariant T (MAIT) cells are innate-like antimicrobial T

234 Mucosal-associated invariant T (MAIT) cells are innate-like T cells enriche

235 Mucosal-associated invariant T (MAIT) cells are MHC-related protein 1 (MR1)

236 Mucosal Associated Invariant T (MAIT) cells can sense intracellular infecti

237 Mucosal-associated invariant T (MAIT) cells have been attracting increasing

238 Mucosal-associated invariant T (MAIT) cells help combat opportunistic infec

239 Mucosal-associated invariant T (MAIT) cells represent a specialized lymphoc

240 y shared between iNKT and mucosal-associated invariant T (MAIT) cells, illustrating a common core dev

241 B-related metabolites to mucosal associated invariant T (MAIT) cells, which are characterized, in pa

242 iated immune dysfunction, mucosal-associated invariant T (MAIT) cells, which have the capacity to res

243 (2) synthesis to activate mucosal-associated invariant T (MAIT) cells.

244 avin-based metabolites to Mucosal-Associated Invariant T (MAIT) cells.

245 K), invariant NKT (iNKT), mucosal-associated invariant T (MAIT), and Vdelta2(+) gammadelta T lymphocy

246 T) are innate-like T cells expressing a semi-invariant T cell receptor restricted to the non-classica

247 1-restricted T cells, and mucosal-associated invariant T cells (MAIT cells) that are restricted to th

248 Mucosal-associated invariant T cells (MAIT) are innate-like T cells express

249 d T cells (DURTs), such as mucosa-associated invariant T cells (MAITs), CD1-restricted T cells, and g

250 Vaccine, TCR Vdelta2, and mucosal-associated invariant T cells expanded after asexual blood-stage par

251 mmadelta cell subsets and mucosal-associated invariant T cells in healthy volunteers immunized with P

252 ; gammadelta T cells; and mucosal-associated invariant T cells in RM from 69 HIV-negative men by flow

253 lation of proinflammatory mucosal-associated invariant T cells was seen for 12 months following AHSCT

254 d by the alphabeta-TCR of mucosal associated invariant T cells, MR1 interacts with specific gammadelt

255 Unlike mucosal-associated invariant T cells, recognition of target cells by the TC

256 uch as NKT, gammadelta T, mucosal-associated invariant T, and CD8alphaalpha T cells, each play distin

257 t from NKT, gammadelta T, mucosal-associated invariant T, and CD8alphaalpha T cells.

258 ent days to test for task- and concentration-invariant taste representations.

259 in transcript levels of the anti-M. marinum invariant TCR rearrangement (iValpha45-Jalpha1.14) and o

260 Furthermore, both the generation of invariant TCRs and the intrathymic acquisition of effect

261 These scale-invariant textures directly reflect the continuous natur

262 -primary areas were substantially more noise-invariant than primary areas.

263 s approach is much faster than other linking invariants, the next step will be evaluation of lassos i

264 ribution quantify two additional topological invariants-the mean orbital spin and the chiral central

265 ver often is portrayed as an abrupt, largely invariant threshold, we found the response to be gradual

266 oduce a new algorithm, Boolean Omics Network Invariant-Time Analysis (BONITA), for signal propagation

267 an end-to-end approach for deriving features invariant to confounding factors while accounting for in

268 The coordinates recovered by our method are invariant to diffeomorphisms of the manifold, making it

269 quasi-first-order biochemical processes are invariant to energy perturbations of the discrete states

270 es hydrolyzed per step is demonstrated to be invariant to energy perturbations of the intermediate st

271 tive for behaviorally relevant stimuli; more invariant to location of stimuli in the visual field; an

272 stems to encode relevant information that is invariant to many stimulus changes is central to normal,

273 roduction declines chronologically with age, invariant to mating activity such that older multiply ma

274 Responses were invariant to motor output (i.e. button press or not), an

275 presentations of letters become increasingly invariant to position and are transformed to convey spok

276 able to external noise by providing response invariant to the absolute intensity emitted from the sen

277 irac and flat bands, endowing a nonzero Z(2) invariant to the flat band.

278 eatures encoded by these neurons and largely invariant to the source of uncertainty.

279 roceeding via these pathways are shown to be invariant to the stability of the intermediates or to th

280 ory central pattern generator as a whole are invariant to these changes of dynamical properties, whic

281 (SOC) is the key to realizing time-reversal-invariant topological phases of matter(1,2).

282 The CFTR gene lies within an invariant topologically associated domain (TAD) demarcat

283 work has established that they exhibit scale-invariant topology, which quantifies the fact that their

284 ination of S-STD slow dynamics and frequency-invariant transmission at faster timescales.

285 In contrast, synapses displaying frequency-invariant transmission can faithfully transfer ongoing p

286 However, rigid frequency-invariant transmission may lead to runaway dynamics and

287 ions of effective non-Hermitian Hamiltonians invariant under simultaneous parity ([Formula: see text]

288 he known laws of physics are not universally invariant under transformation of scale.

289 The computed edge states and Z(2) invariants underpin the non-trivial topological properti

290 les of many protein sequences remain largely invariant upon frameshifting.

291 tions upon turning voltage on and off is not invariant upon reversal of time, prompting lateral trans

292 ositive pig cells predominantly expressed an invariant Valpha-Jalpha rearrangement, without nontempla

293 stead, mixed dynamics supported robust, time invariant value representations while also encoding the

294 t surface roughness approaches an asymptotic invariant value that follows power law behavior as a fun

295 rise two distinct types: those expressing an invariant Vgamma6Vdelta1(+) TCR and those expressing a V

296 i phase shows a lattice contraction which is invariant with cooling rate.

297 We find the CO production rate to be invariant with pH on a Standard Hydrogen Electrode scale

298 ic obeys an inverse exponential law which is invariant with the size of the vehicle fleet.

299 ses can be strikingly malleable, rather than invariant, with changes in the visual characteristics of

300 ne response" as a notably prominent, largely invariant, yet distinctive force at the forefront of pat