ライフサイエンスコーパス: oppositely

1 d acetylation regulate Drosha protein levels oppositely.

2 put pathways via the concerted action of two oppositely acting enzymes.

3 atalyzes monoglucosylation of N-glycans, and oppositely acting glucosidase II (GlucII), and that vIL-

4 Thus ADAMTS10 and ADAMTS6 oppositely affect heparan sulphate-rich interfaces inclu

5 ion response of lateral roots appeared to be oppositely affected by abscisic acid signaling compared

6 rocesses degraded by this syndrome are often oppositely affected by calorie restriction, which extend

7 ly growth response 1 and Smad3/4, which were oppositely affected by GSK-3alpha or GSK-3beta silencing

8 Surprisingly, dlx4b and dlx3b are oppositely affected in mef2ca mutants.

9 roles in skeletal muscle gene expression by oppositely affecting the subcellular localization of HDA

10 eceptor, selectively from D1+ or D2+ neurons oppositely affects cocaine reward.

11 reveal a neurobiological control system that oppositely affects internalization and overt compliance.

12 dentify a KLF4-miR-206 feedback pathway that oppositely affects protein translation in normal cells a

13 e at the boundary of neighbouring regions of oppositely aligned magnetic dipoles, their equivalent in

14 The spins are aligned oppositely along out-of-the-plane direction at the K and

15 estriction (FR) and an obesogenic (OB) diet, oppositely alter the sensitivity of striatal DA release

16 adiponectin and leptin are independently but oppositely associated with coronary artery calcification

17 LT3-ITD+ were negatively associated and were oppositely associated with presenting white blood count

18 Oppositely biased pumping electrodes, consisting of 2.5

19 microm, attained between electrodes that are oppositely biased.

20 that oligodendrocyte apoptosis is regulated oppositely by c-Jun N-terminal kinase 3 (JNK3) and prote

21 dgroups and at the lipid tails are modulated oppositely by cholesterol, explaining the experimental f

22 ion with ARFGAP1, which is in turn regulated oppositely by p-coA and nicotinamide adenine dinucleotid

23 We assess the oppositely changing effects of tobacco on male and femal

24 ity wave couples to twist distortions of the oppositely charged actin filaments.

25 gative corona to generate ions to neutralize oppositely charged aerosols generated by electrospray an

26 ing highly conserved charged residues to the oppositely charged amino acid had an increased likelihoo

27 dues, Glu-42 and Lys-89, which interact with oppositely charged amino acid residues buried in a large

28 AA4 features two distinct surface patches of oppositely charged amino acid residues, mediating front-

29 study, we investigated the adsorption of the oppositely charged amino acids glutamate and lysine with

30 require an electrostatic interaction between oppositely charged amino acids within their G loops that

31 idney (kNBC1) were mutated to neutral and/or oppositely charged amino acids.

32 by the unique stereochemical arrangement of oppositely charged amino and carboxy groups.

33 Simultaneous application of oppositely charged amphipaths generally results in no ne

34 e into the membrane to enable alignment with oppositely charged aspartate residues within CD3zeta and

35 Long-lived excited states are shown to be oppositely charged base pair radical ions.

36 rged lipids and membrane proteins, fuse with oppositely charged bilayers, with no requirement for det

37 Driving forces for association between oppositely charged biological or synthetic polymers in a

38 on its strong electrostatic interaction with oppositely charged C-terminal tails of the HBcAgs, and t

39 (3) than for X = CH(3), despite the strongly oppositely charged carbon atoms of the CF(3) (+0.79e) an

40 ediated hydrogen bonding interaction between oppositely charged carboxylic acid and amine functionali

41 Electrostatic forces cause the oppositely charged cationic conjugated polymer to bind s

42 lecules can aggregate under the influence of oppositely charged condensing agents, the specific condi

43 ng, as well as unbinding and annihilation of oppositely charged disclination defects.

44 The natural alignment of oppositely charged domains as two such surfaces approach

45 Utilizing the complementarity of oppositely charged domains in short collagen-like peptid

46 e speculated that ionic interactions between oppositely charged domains of MARCKS were responsible fo

47 The results are compatible with shielding of oppositely charged domains that move through the solvent

48 to a strong electrostatic attraction between oppositely charged droplets (0mM NaCl, pH 7, 25 degrees

49 on as well as in microfluidic devices, where oppositely charged droplets are forced to collide within

50 We observe noncoalescence of oppositely charged droplets in bulk emulsification as we

51 lizers, we prepare emulsions that consist of oppositely charged droplets, which do not coalesce.

52 ning of the electrostatic attraction between oppositely charged droplets.

53 The observation of oppositely charged drops bouncing rather than coalescing

54 nce of a critical field strength above which oppositely charged drops do not coalesce.

55 tendency for adjacent drops to coalesce, and oppositely charged drops have long been assumed to exper

56 We observe that appropriately positioned and oppositely charged drops migrate towards one another in

57 th the theoretical predictions for a pair of oppositely charged electric or magnetic monopoles.

58 d dye-modified lipid in the direction of the oppositely charged electrode.

59 igh sensitivity to fluorescence quenching by oppositely charged electron acceptors; in this study, 9,

60 Oppositely charged electron and hole quasiparticles can

61 relative roles of the aromatic residues and oppositely charged end groups in stabilizing the earlies

62 Additionally, incorporation of oppositely charged fluorophores into the barrel investig

63 Salt-bridges between oppositely charged Glu(-) and Lys(+) side chains can, in

64 at the apolar sides face each other, and the oppositely charged groups may form salt links, which are

65 for characterizing selective binding between oppositely charged ionic functional groups under biologi

66 copolypeptides were designed to incorporate oppositely charged ionic segments that form beta-sheet-s

67 To enable mutual storage of oppositely charged ions in a linear ion trap, the oscill

68 cally, the water-mediated attraction between oppositely charged ions is enhanced relative to that in

69 taken to enable the simultaneous storage of oppositely charged ions.

70 polymorphism of two-dimensional crystals of oppositely charged linear macroions, namely DNA and self

71 gnaling processes, they can attract or repel oppositely charged lipids.

72 to be in a condensed state, most likely with oppositely charged macro-ion condensing agents from the

73 important problem; unwanted adhesion between oppositely charged materials, spark-initiated explosions

74 tion between charged peripheral proteins and oppositely charged membranes.

75 ace area through aggregation mediated by the oppositely charged metal ions and suppressing zinc ion r

76 anionic small molecules were enriched using oppositely charged micelles from sodium dodecyl sulfate

77 be assembled by applying DEP to mixtures of oppositely charged microspheres.

78 edra with diverse symmetries by coassembling oppositely charged molecules of different stoichiometric

79 lyte dendrimers of different generations and oppositely charged multivalent organic dyes relying on t

80 Solutions containing oppositely charged nanoparticles (NPs) deposit "patchy"

81 Here, we show that oppositely charged nanoparticles can function as univers

82 rystals, in which each nanoparticle has four oppositely charged neighbors.

83 nderstanding of the stability of crystals of oppositely charged particles.

84 butions to stability were not equivalent for oppositely charged partners in ion pairs, suggesting tha

85 h potential for ionic bond formation between oppositely charged partners.

86 Mixing a 1:1 ratio of two oppositely charged peptoid 36mers of a specific sequence

87 nsient chemical species by inducing nascent, oppositely charged photochemical products to migrate in

88 epared by the electrostatic self-assembly of oppositely charged poly(L-lysine) (PL) and silica nanopa

89 relationship aids in the rational design of oppositely charged polyelectrolyte-surfactant formulatio

90 Oppositely charged polyelectrolyte-surfactant mixtures a

91 psule shell is formed by the complexation of oppositely charged polyelectrolytes at the immiscible in

92 junction between two aqueous gels containing oppositely charged polyelectrolytes could rectify electr

93 ormed by the associative phase separation of oppositely charged polyelectrolytes into polyelectrolyte

94 fects are created by simultaneously spraying oppositely charged polyelectrolytes that induce surface

95 he parameters where layer-by-layer growth of oppositely charged polyelectrolytes was possible because

96 ough selective, sequential adsorption of the oppositely charged polyelectrolytes, sodium poly(styrene

97 (PEC) are formed by mixing the solutions of oppositely charged polyelectrolytes, which were hitherto

98 in and (2) the Columb attraction between the oppositely charged polyelectrolytes.

99 LbL involved alternate adsorption of the oppositely charged polyions from dilute aqueous solution

100 nsisting of alternating nanometric layers of oppositely charged polyions, poly(diallyldimethylammoniu

101 sticking of particles at the vertices of the oppositely charged polymer networks.

102 coacervation method using the interaction of oppositely charged polymers as gelatin/gum arabic and ge

103 -scale lattice spacings have been grown from oppositely charged polymethyl methacrylate spheres.

104 exes, formed from mixing dilute solutions of oppositely charged polypeptides, via a combination of el

105 diffusion contribute to protein transport in oppositely charged porous materials and may be exploited

106 teristics by controlled heteroaggregation of oppositely charged protein-coated lipid droplets.

107 s such as PIP(2) more quickly segregate near oppositely charged proteins than do monovalent lipids, e

108 g electrostatic interactions between the two oppositely charged proteins.

109 dues Lys-10 and the N terminal interact with oppositely charged receptor residues only at the alphade

110 el where the interplay between 7SK snRNA and oppositely charged regions in HEXIM1 direct its binding

111 , each surface supports a random "mosaic" of oppositely charged regions of nanoscopic dimensions.

112 ttractive electrostatic interactions between oppositely charged regions on adjacent DNP surfaces.

113 In addition, a pair of oppositely charged residues (Arg/Glu), forming a salt br

114 ng six cysteines, one glycine, and a pair of oppositely charged residues Arg/Glu, are conserved in th

115 The presence of a pair of oppositely charged residues at the aforementioned positi

116 ions with steroid receptors are modulated by oppositely charged residues flanking the motifs and char

117 ectivity of SPICE and VCP is the presence of oppositely charged residues in the central complement co

118 t of peptides, the distance and order of the oppositely charged residues in the peptide sequence diff

119 Increased segregation of oppositely charged residues leads to linear decreases in

120 hat electrostatic interactions between these oppositely charged residues of TM4 and protein C facilit

121 xperimental values when there are strings of oppositely charged residues or concentrations of like ch

122 s poorly conserved, the linear patterning of oppositely charged residues shows minimal variation.

123 Segregation of oppositely charged residues within linear sequences lead

124 We identify a pair of oppositely charged residues, E153 and R169, that compris

125 bular protein, ubiquitin, contains a pair of oppositely charged residues, K11 and E34, that according

126 ues and the linear sequence distributions of oppositely charged residues.

127 to be influenced by the linear patterning of oppositely charged residues.

128 -mediated charge-charge interactions between oppositely charged side chains and between oppositely ch

129 Salt bridges between oppositely charged side chains are well-known to stabili

130 s of R596 strengthen our hypothesis that the oppositely charged side chains of the DPPR peptide in Na

131 rm that silica nucleation is most rapid when oppositely charged species are proximal.

132 to be detected free from interferences from oppositely charged species, enabling positive and negati

133 bution of metal counterions binding onto the oppositely charged surface of a model polyelectrolyte, n

134 boelectrically charged glass particles on an oppositely charged surface of a plastic cylindrical cont

135 ed and that cooperative interactions between oppositely charged surface species play important roles

136 aggregate, due to steric complementarity of oppositely charged surfaces on the domain, but this is i

137 expected, due to electrostatic attraction of oppositely charged surfaces, only little adsorption was

138 roles in the adsorption of charged lipids on oppositely charged surfaces.

139 nted with a binding partner, in this case an oppositely charged surfactant, changes in solvent microe

140 n oppositely charged side chains and between oppositely charged termini, with forces between aromatic

141 Assembly of oppositely charged triblock copolyelectrolytes into phas

142 The self-assembly of the oppositely charged water-soluble porphyrins, cobalt tetr

143 e charge binding between M13 viruses and two oppositely charged weak polyelectrolytes leads to interd

144 rred when the Schiff base and residue 85 are oppositely charged, a bent chromophore is found when bot

145 For example, for proteins that are oppositely charged, a combination of a large transmembra

146 ental insight into heteroaggregation between oppositely charged, and between neutral and charged nano

147 residues involved in these interactions are oppositely charged, and their sequence conservation sugg

148 t pH values where Cit-AuNPs and hematite are oppositely charged, attachment efficiencies are high and

149 achieved if the channel and the protein are oppositely charged.

150 a-helical polypeptides to self-assemble with oppositely-charged polypeptides to form liquid complexes

151 omoallene installation allowed access to the oppositely configured 12,13-epoxides of 12-epoxyobtusall

152 ult from the photointerconversion of the two oppositely connected SRI-HtrI conformers by one-photon a

153 ify orthogonal neuromodulatory cascades that oppositely control peripheral taste sensitivity for each

154 genes similarly regulate LGE patterning but oppositely control the balance between proliferation and

155 These transcription factors directly and oppositely control the expression of the gene encoding P

156 t the synthesis of flagella and fimbriae are oppositely controlled.

157 emory of familiar positions were equally and oppositely correlated with amounts of TR sleep.

158 Spontaneous and evoked transmission were oppositely correlated with presynaptic levels of the pro

159 olet images clearly shows that two groups of oppositely directed and non-coplanar magnetic loops grad

160 y meet and form gap junctions (GJs) with the oppositely directed axons of their segmental homologs, s

161 ysical changes that bias competition between oppositely directed fast- and slow-activating conductanc

162 that frequently occurs when plasmas carrying oppositely directed field lines collide.

163 eaked at approximately 200 ms followed by an oppositely directed larger component that peaked at appr

164 ch reconnection X-line (the line along which oppositely directed magnetic field lines reconnect) exte

165 cular machines consisting of two coupled and oppositely directed motile elements which extrude loops

166 They possess oppositely directed plasma jets emanating at near light

167 y manifested in split energy dispersions for oppositely directed plasmon waves.

168 Oppositely directed projections of some homologous neuro

169 by measurements of the reversal potential at oppositely directed salt gradients.

170 These oppositely directed shifts indicate that the mutation mo

171 nal compression force equal in magnitude but oppositely directed to the stretching (tension) force on

172 separate sets of genes and extend axons with oppositely directed trajectories; anterior (DA) versus p

173 myosin and TnI compete for actin and induce oppositely-directed chain kinks.

174 myosin light polypeptide 4 (Myl4)] that were oppositely expressed (q < 0.05) between EdnrB (-/+) and

175 s has suggested that a regulatory circuit of oppositely expressed bmp4 and admp genes represents a de

176 Imprinting of the linked and oppositely expressed mouse H19 and Igf2 genes requires a

177 is-37 residues in the tetramer stabilizes an oppositely gated Closed(out)-Open(in) conformation.

178 cked domains, or at the line junction of two oppositely gated regions.

179 tructure comprises two distinct regions with oppositely handed helices separated by a short disordere

180 locus is highly complex and encodes several oppositely imprinted and alternatively spliced transcrip

181 yndrome (PWS) and Angelman syndrome (AS) are oppositely imprinted autism-spectrum disorders with know

182 Do insulin (or IGF-1) and glucagon act oppositely in controlling eye growth, as they do in meta

183 indicator genes that change their expression oppositely in mouse binucleate ventricular cardiomyocyte

184 ic and postsynaptic proteins are distributed oppositely in relation to the tonotopic map and that the

185 Oppositely, in a checkpoint-triggering aberrant situatio

186 n the nanoscale, however, this is often done oppositely: individual macromolecules are manipulated by

187 ion proteins with EAL and GGDEF domains that oppositely influence motility and biofilm formation.

188 ntext-specific BR activity and responses are oppositely interpreted at the organ level, ensuring cohe

189 Oppositely labeled probes diffused across the initial fr

190 separate 16-h hybridization experiments with oppositely labeled probes premixed, arrays that were con

191 Oppositely, loss of all ECM components (DeltawcaM Deltac

192 wer moment Mn-Ge termination layers that are oppositely magnetized to the higher moment Mn-Mn layers.

193 the same sign, even though these layers are oppositely magnetized, high-tunnelling magnetoresistance

194 r-regulated Smads (R-Smads): Smad2 and Smad3 oppositely modify STAT3-induced transcription of IL-17A

195 ese results demonstrate that dSPNs and iSPNs oppositely modulate both therapeutic and dyskinetic resp

196 striatal projection neurons are proposed to oppositely modulate cortical activity via BG outputs to

197 ound C or activation using an AMPK activator oppositely modulated APAP cytotoxicity, suggesting that

198 Mixing of oppositely mutated PsIAA4 PB1 monomers enabled NMR mappi

199 ve of the potential of zero charge (pzc) and oppositely negative of the pzc.

200 dissociation inhibitor act independently but oppositely on Cdc42.

201 ) and vascular endothelial growth factor act oppositely on endothelial cell junctions.

202 ression; and in general, GATA1 and GATA2 act oppositely on switch target genes.

203 the proteins form parallel dimers only if no oppositely orientated partner is present.

204 Co-expression of oppositely orientated proteins almost exclusively yields

205 w a number of zigzag connections between the oppositely oriented actin filaments.

206 led Z-links, probably alpha-actinin, between oppositely oriented actin filaments.

207 beta-strands, S5, S6, and S7, flanked by two oppositely oriented alpha-helices, H3 and H4.

208 es reside in about the same position but are oppositely oriented and defective relative to the IS1470

209 en gene fragments are positioned between two oppositely oriented and functionally active promoters.

210 h of the 16 yeast centromeres is occupied by oppositely oriented Cse4/H4/H2A/H2B hemisomes in two rot

211 Oppositely oriented DNA on parallel binding sites of the

212 ace of the DNA helix by interaction with two oppositely oriented essential arrays of closely spaced l

213 ositely oriented signals that are encoded by oppositely oriented Fj and Ds gradients produce the same

214 ergized by the transmembrane pH gradient and oppositely oriented gradients of the other cation substr

215 These results are consistent with oppositely oriented gradients of these two neurotrophins

216 d indicate that distinct mechanisms load the oppositely oriented helicases that are central to bidire

217 of terminal base pairing in end joining, two oppositely oriented HO endonuclease cleavage sites separ

218 within the intron of the 5'-overlapping but oppositely oriented latent-state transcription unit for

219 spindle fusion is dynein-mediated sliding of oppositely oriented microtubules, a novel function for t

220 ms coordinating the collective activities of oppositely oriented motors bound to the same cargo are n

221 entially through direct interactions between oppositely oriented motors.

222 evidence that MT plus end interactions from oppositely oriented organizing centers can provide the f

223 However, in M.laminosus, TDS binds in an oppositely oriented ring-out mode, with the tail inserte

224 Oppositely oriented signals that are encoded by opposite

225 tional approaches with functional studies of oppositely oriented single channels within the same lipi

226 transmembrane segments (TMS) with a pair of oppositely oriented, conserved sequences called the alph

227 mediating the expression of both ATE1 and an oppositely oriented, previously uncharacterized gene.

228 Here, we show that oppositely patterned and antagonistic actions of BR and

229 based on applying a cell voltage between two oppositely placed porous carbon electrodes.

230 ay of the surface potential contrast between oppositely polarized domains.

231 ifferences in the synaptic signaling between oppositely polarized hair cells.

232 e first time that cytokine production can be oppositely polarized in different organs of the same ind

233 in a reinforcing flow configuration between oppositely polarized sets of pumping electrodes with app

234 copy data indicate that these hooks can join oppositely protruding Rad50 coiled-coil domains to form

235 racterized for their roles in plant defense, oppositely regulate Arabidopsis pollen tip growth with S

236 f hypothalamic neurons, including those that oppositely regulate body weight, are specialized as near

237 ivo, our results suggest that IL-15 and IL-2 oppositely regulate CX3CR1 gene expression by differenti

238 d IL-2, which signal through IL-2Rbetagamma, oppositely regulate expression of the proinflammatory ch

239 ant mechanism by which interoceptive neurons oppositely regulate homeostatic drives to eat and drink.

240 e both water and sugar abundance signals and oppositely regulate hunger and thirst.

241 s of the basal ganglia have been proposed to oppositely regulate locomotion and differentially contri

242 positely regulated by starvation and in turn oppositely regulate lysosomal biogenesis and autophagy,

243 We show that IL-2 and TGF-beta1 oppositely regulate NKG2D-DAP10 expression by NK cells.

244 transcription factor Orthodenticle (Otd) to oppositely regulate R7 and R8 PR Rhodopsin gene expressi

245 from those triggered by LPS, as both agents oppositely regulate the expression of CCL19 and TRIB3 Be

246 ediated by LIMK and SSH, respectively, which oppositely regulate the phosphorylation-dependent asymme

247 strate that macula densa COX-2 expression is oppositely regulated by AT(1) and AT(2) receptors and su

248 t, whereas AWC coupling to motor circuits is oppositely regulated by aversive and appetitive learning

249 rcuate nucleus of the hypothalamus (ARC) are oppositely regulated by caloric depletion and coordinate

250 we show that proliferation and invasion are oppositely regulated by CSF1R downstream of TGFbeta only

251 NK to regulate this apoptotic process and is oppositely regulated by JNK1 and JNK2.

252 identified multiple mitochondrial substrates oppositely regulated by parkin and USP30.

253 orophyll and carotenoids, hallmark processes oppositely regulated by PIF1.

254 Distinct insertion modes were oppositely regulated by receptor activation and by mecha

255 These CCCs are oppositely regulated by serine-threonine phosphorylation

256 mal biogenesis cluster are transcriptionally oppositely regulated by some common machinery.

257 Interestingly, ZKSCAN3 and TFEB are oppositely regulated by starvation and in turn oppositel

258 n this circuitry is the TRIB2 gene, which is oppositely regulated by TAL1 and E2A/HEB and is essentia

259 ensus sequences in their promoters, are also oppositely regulated by the D1 and D3 receptors after re

260 We found that stress susceptibility is oppositely regulated by the specific cell type and HPTM

261 plicing of hundreds of alternative exons was oppositely regulated by these proteins, confirming an ad

262 s, as well as the same promoter activity was oppositely regulated by two different SlNACMTF.

263 Importantly, MED23-coupled H2Bub levels are oppositely regulated during myogenesis and lung carcinog

264 = 24) in both equol-producing phenotypes and oppositely regulated expression for equol producers (dow

265 ession of CCL19 and expression of CCL21 were oppositely regulated, and myeloid dendritic cells upregu

266 ulation, the expressions of DCT and CAV1 are oppositely regulated; DCT increases while CAV1 decreases

267 Here, we show that MAX2 oppositely regulates GA and ABA biosynthesis to optimize

268 That AphA oppositely regulates the expression of pva from that of

269 ne novel discovery is that OpaR strongly and oppositely regulates two type VI secretion systems (T6SS

270 nown as FUSE, and influence transcription by oppositely regulating TFIIH at the promoter site.

271 hanism involving the whole of the C terminus-oppositely shape the kinetics and sensitivity of the non

272 utation to aspartate, however, results in an oppositely shifted and split heme a EPR signal of g(z) =

273 mode pairs come in skew-symmetric pairs with oppositely signed eigenvalues.

274 he warm season as continental-scale pairs of oppositely signed precipitation and temperature anomalie

275 large friction barrier against the merge of oppositely supercoiled DNA domains.

276 Thus, whereas oppositely supercoiled domains are generated in a tetA-b

277 The diffusional merge of these oppositely supercoiled domains is not significantly affe

278 C and L42C are likely to point approximately oppositely, these two cross-links are likely to favor si

279 to tilted lines can make vertical lines seem oppositely tilted (the tilt aftereffect).

280 g that PKC-delta and PKC-alpha/beta function oppositely to facilitate cells harboring v-ras to surviv

281 of gro is surprising, because it is directed oppositely to its traditionally defined role as a neurog

282 First, we show that hexadecanol acts oppositely to n-alcohol anesthetics on membrane mixing a

283 ty defect, indicating that ULT1 and KAN1 act oppositely to regulate the adaxial-abaxial axis.

284 ity of the Arabidopsis life cycle, ULT1 acts oppositely to STM and WUS in maintaining meristem activi

285 ependent Gln3 dephosphorylation is regulated oppositely to that of Sit4, being greatest in Pro- and l

286 ts in resistance decrease, which is directed oppositely to the background.

287 vation of thumb movements that were oriented oppositely to the previously determined habitual directi

288 required for Vi capsular antigen expression oppositely to those required for motility and invasion.

289 d in early somite-stage embryos that respond oppositely to treatment with RA versus RA antagonists an

290 cally disruptive if interacting taxa respond oppositely to warming.

291 the pathogenic LRRK2(G2019S) allele behaves oppositely to wild-type lrrk in that it promotes rather

292 In contrast, the Ras pathway acts oppositely, to promote YAP1 stability through downregula

293 tide synthesis on diagnostic microarrays or, oppositely, to the large-scale preparation of therapeuti

294 binding site in the substrate-free form, but oppositely, toward the proposed proton delivery shuttle,

295 te direction responses as those of a pair of oppositely tuned neurons and (2) computing the vector av

296 ed spike-count correlations between pairs of oppositely tuned neurons.

297 are the key: the opponent subtraction of two oppositely tuned stages that individually have sinusoida

298 ormalization model containing populations of oppositely tuned, mutually suppressive neurons explains

299 echanistic corollary is that closely spaced, oppositely winding spirals merge to form concentric loop

300 pliced and that the splice variants function oppositely, with the longer transcript (ced-4L) inhibiti