ライフサイエンスコーパス: oppositely

1 d acetylation regulate Drosha protein levels oppositely.

2 affected when the electrons are transported oppositely.

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

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

5 we report a methane nano-trap that features oppositely adjacent open metal sites and dense alkyl gro

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

7 , (S)-(+)- and (R)-(-)-linalool, reported to oppositely affect M. sexta oviposition, in the Arizona a

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

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

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

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

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

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

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

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

16 brogating CA1->RSCg or ATN->RSCg connections oppositely affects the encoding of contextual fear memor

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

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

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

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

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

22 alyses reveal that the expression of CsTA is oppositely associated with the accumulation of galloylat

23 osing tension in the chromatin that connects oppositely attached sister chromatids, which may then ac

24 Oppositely biased pumping electrodes, consisting of 2.5

25 microm, attained between electrodes that are oppositely biased.

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

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

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

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

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

31 irs are key stabilizing interactions between oppositely charged amino acid side chains in proteins.

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

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

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

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

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

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

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

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

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

41 ged blocks and number of connections between oppositely charged blocks are shown to have a dramatic e

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

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

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

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

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

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

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

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

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

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

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

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

54 ning of the electrostatic attraction between oppositely charged droplets.

55 The observation of oppositely charged drops bouncing rather than coalescing

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

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

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

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

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

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

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

65 nionic surfactants, composed of a mixture of oppositely charged ionic surfactants without their origi

66 gers, CLCs uniquely catalyze the exchange of oppositely charged ions (Cl(-) for H(+)).

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 pKa of D97 observed from PR reconstituted in oppositely charged liposome environments disappeared whe

73 a function of pH strongly depend on whether oppositely charged macromolecules or neutral macromolecu

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

75 tion between charged peripheral proteins and oppositely charged membranes.

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

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

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

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

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

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

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

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

84 that like-charged monopoles attract whereas oppositely charged ones repel, unlike in electrostatics(

85 ls based on ion-exchange interactions of the oppositely charged paper (protonated tertiary amine grou

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

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

88 itively simple idea of forming crystals from oppositely charged partners, instead forming non-equilib

89 paces and often involve interactions between oppositely charged peptide domains.

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

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

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

93 Oppositely charged polyelectrolyte-surfactant mixtures a

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

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

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

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

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

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

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 e SH3(5) (S) and PRM(5) (P), two pentameric, oppositely charged protein constructs; heparin (H), an a

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

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

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

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

113 ype p27 IDR (kappa31) and kappa14, where the oppositely charged residues are more evenly distributed,

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

115 nal consequences of the linear patterning of oppositely charged residues because it measures and sepa

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

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

118 d evidence for pairwise interactions between oppositely charged residues in the receptor and chemokin

119 contrast, kappa56 with linear segregation of oppositely charged residues leads to limited conformatio

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

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

122 Segregation of oppositely charged residues within linear sequences lead

123 the linear segregation versus clustering of oppositely charged residues within the primary sequence.

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

125 xtent of linear mixing versus segregation of oppositely charged residues.

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

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

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

129 lectrostatic interactions of the latter with oppositely charged sites on the cationic surfactant head

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

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

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

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

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

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

136 ition-via electrostatic interactions between oppositely charged surfaces.

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

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

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

140 Assembly of oppositely charged triblock copolyelectrolytes into phas

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

161 They possess oppositely directed plasma jets emanating at near light

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

163 Oppositely directed projections of some homologous neuro

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

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

166 These teleconnections generate oppositely directed trade-wind anomalies in the Central

167 iochemical excitability: the annihilation of oppositely directed waves, all-or-none responsiveness, a

168 al breakdown in thunderstorms can begin with oppositely-directed fast breakdown of negative polarity,

169 e equator when magnetic dams, created by the oppositely-directed old cycle's toroidal field in North

170 C-CREB signaling pathways, the biotypes were oppositely dysregulated, suggesting that the biotypes we

171 in mice revealed that these two populations oppositely encode positive and negative motivational val

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

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

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

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

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

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

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

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

180 Oppositely, in a checkpoint-triggering aberrant situatio

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

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

183 filled d-orbitals (groups 11 and 12) behave oppositely; initially the M-M bond is covalent, but upon

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

185 Oppositely labeled probes diffused across the initial fr

186 Oppositely, loss of all ECM components (DeltawcaM Deltac

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

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

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

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

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

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

193 Mixing of oppositely mutated PsIAA4 PB1 monomers enabled NMR mappi

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

195 dissociation inhibitor act independently but oppositely on Cdc42.

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

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

198 ridges and near-cofacial packing motifs with oppositely or parallel pai-stacked structures depending

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

200 Co-expression of oppositely orientated proteins almost exclusively yields

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

202 at takes advantage of the combination of two oppositely oriented coaxial domes, providing an opportun

203 ed on a theoretical model that considers two oppositely oriented coupled domains, this high-frequency

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

205 ior to the movement initiation in one of two oppositely oriented directions along the rostro-caudal a

206 Oppositely oriented DNA on parallel binding sites of the

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

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

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

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

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

212 ive time-lapse microscopy, we identified two oppositely oriented nuclear migrations that precede and

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

214 n pairing adopt similar orientations and are oppositely oriented relative to thiocyanate ions near ne

215 Oppositely oriented signals that are encoded by opposite

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

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

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

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

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

221 rating a negative feedback loop, the signals oppositely polarize, establishing sharp boundaries and c

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

223 These results demonstrate that oppositely polarized electronically excited states can b

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

225 t that crosses the gap between two arrays of oppositely polarized microelectrodes, generating a magne

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

227 drolysis, featuring hydrolytic events in two oppositely positioned ATPases, in two adjacent ATPases a

228 iated with effort activation and discounting oppositely predicted striatal encoding of effort during

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

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

231 era titer, we found that aphids and Buchnera oppositely regulate genes underlying amino acid biosynth

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

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

234 vered that pro- and anti-inflammatory agents oppositely regulate KLF6 and miR-223 expression in macro

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

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

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

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

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

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

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

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

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

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

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

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

247 We have found that neuronal NKA activity is oppositely regulated by phosphorylation and dephosphoryl

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

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

250 These CCCs are oppositely regulated by serine-threonine phosphorylation

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

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

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

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

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

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

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

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

259 transcriptional response composed of large, oppositely regulated gene clusters.

260 ion factor Egr3 (early growth response 3) is oppositely regulated in nucleus accumbens (NAc) cell sub

261 FnrS and ArcZ are oppositely regulated in response to oxygen, one of the k

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

263 TRANSPORTER2;1 and SUCROSE TRANSPORTER4 were oppositely regulated, leading to the mobilization of sug

264 CAGE) signature, in which many ESR genes are oppositely regulated.

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

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

267 Ectopic expression of GhDsPTP3a and GhANN8b oppositely regulates plant salt tolerance and calcium in

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

269 activity in young adults was associated with oppositely regulating HOXB1 and HOXA3 methylation compar

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 We show that dopamine oppositely shapes responses to convergent excitatory inp

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

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

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

276 Oppositely, slowing of pore kinetics by the SNARE-regula

277 ly of this structure suggests that combining oppositely supercharged pairs of protein variants may pr

278 symmetrical oligomers by combining pairs of oppositely supercharged variants of a normally monomeric

279 Oppositely, the attempts to synthesize these gamma-cyano

280 Oppositely, the unique role of Rad61/Wapl is to promote

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

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

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

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

285 Oppositely to overexpression, ANKRD9 knockdown increases

286 nter for male sexual behaviors, and function oppositely to regulate multiple arousal-related behavior

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

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

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

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

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

292 cally disruptive if interacting taxa respond oppositely to warming.

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

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

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

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

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

298 Oppositely, we establish that p190A is obligatory for E-

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