ライフサイエンスコーパス: opposing effect

1 sponsiveness, SLC1A5/38A2 knockdown elicited opposing effects.

2 ociated genes were observed, many times with opposing effects.

3 yclase to cAMP to protein kinase A--but with opposing effects.

4 larified how the same receptor mediates such opposing effects.

5 ing, with Ala and Asp substitutions inducing opposing effects.

6 having profibrotic effects and others having opposing effects.

7 whereas inhibition by Dkk1 (Dickkopf-1) had opposing effects.

8 d that an early-career setback has powerful, opposing effects.

9 ine is a signaling nucleoside with potential opposing effects; adenosine can either protect against a

10 define a novel regulatory mechanism of GDFs' opposing effects and their relevance in RGC differentiat

11 The mechanisms underlying these opposing effects appear to be fundamentally distinct.

12 We find these opposing effects are due in part to GDF-15's ability to

13 How these opposing effects are integrated to impact immune checkpo

14 These opposing effects are suited to prevent premature cleavag

15 How an optimal balance between these opposing effects arises is not well characterized.

16 noninvasive electrical stimulation, we show opposing effects at beta and gamma frequencies and inter

17 invade the parenchyma during pathology; the opposing effects (beneficial or detrimental) of these ce

18 DRG neuron activation by chloroform and the opposing effects chloroform has on different TRP channel

19 Such opposing effects depend on whether synapses persist or d

20 critically affects skin carcinogenesis with opposing effects early and late in tumorigenesis.

21 TOMM40, TCF7L2, and CETP variants, many with opposing effects (eg, the same rs7901695/TCF7L2 allele i

22 iators of arthritis, suggesting reciprocally opposing effects either via NF-kappaB or at the genomic

23 tion was determined by a balance between two opposing effects: enhanced presynaptic vesicular release

24 lung cell proliferation postnatally but had opposing effects following hyperoxia.

25 WT enzyme the Trp(66) residue balances these opposing effects for optimal catalysis.

26 A, consistent with the recent recognition of opposing effects for these phytohormones on the microbia

27 determined by nuclear stiffness, as well as opposing effects from actin and intermediate filaments.

28 phin release, which inactivates the DAP, the opposing effects generating successive periods of bursti

29 has attracted considerable attention for its opposing effect in carcinogenesis as tumor suppressor (e

30 ty acid (VLCFA) derangement has dramatically opposing effects in astrocytes and oligodendrocytes.

31 that NF-kappaB and p53, which generally have opposing effects in cancer cells, coregulate induction o

32 ngs show that VAP-1 and alpha4 integrin have opposing effects in Con A-induced hepatic injury, which

33 For example, TLR7 and TLR9 have opposing effects in mouse models of systemic lupus eryth

34 to determine the relative strength of these opposing effects in natural wetland communities.

35 t cholinergic regulation produced strikingly opposing effects in output and intrinsic neurons.

36 riasis have distinct genetic mechanisms with opposing effects in shared pathways influencing epiderma

37 n species (ROS) and antioxidants, which have opposing effects in the cell, ultimately influence RAS-m

38 SRSF1) to understand the foundation of these opposing effects in the nucleus.

39 similar affinities, and why SAP and CRP have opposing effects is unknown.

40 is found that PEGylated DNA experiences two opposing effects: local excluded volume effect and chemi

41 Conversely, opposing effects occur with miR-515-5p inhibition and by

42 centers near pillar edges while avoiding the opposing effect of confinement.

43 The opposing effect of Jade-1 phosphorylation by CK1alpha su

44 actions through MOR and DOR may underlie the opposing effect of these receptor systems on anxiety and

45 This is the first report of spatiotemporal opposing effects of a host lectin for a virus in one typ

46 g RNAi to zebrafish and reveal unanticipated opposing effects of a seed mismatch with implications fo

47 The opposing effects of ATO and MPH in the NAcb core and she

48 sms for regulating atRA biosynthesis and the opposing effects of atRA and insulin on gluconeogenesis,

49 ional variability, which we attribute to the opposing effects of austral summer insolation and the te

50 We also report opposing effects of bicuculline and gabazine, such that

51 thesised that inhibin alpha may modulate the opposing effects of BMP and inhibin on androgen producti

52 ncentration and composition, we observed the opposing effects of cardenolides on monarch fitness trai

53 of Neuron, Griciuc et al. (2019) demonstrate opposing effects of CD33 and TREM2 on AD phenotypes, whe

54 nscription-PCR (RT-PCR) validation indicated opposing effects of CGI methylation in transcriptional r

55 CTCF clusters in living cells, uncovers the opposing effects of cohesin and transcription on CTCF cl

56 ical pathways affected by 5AR inhibition and opposing effects of COX-2 on the tissue-protective actio

57 These strain-dependent opposing effects of DOM were also observed with glutathi

58 Thus, H3 methylation exerts opposing effects of enhancing nucleosome acetylation by

59 In conclusion, the opposing effects of environmental DNA damage and DNA rep

60 asma 8-isoprostane F2alpha analysis revealed opposing effects of FO (increased) and AO (reduced) comp

61 y a pivotal role for polyadenylation and the opposing effects of Gld2 and Ngd in hippocampal synaptic

62 s sensitivity to image recurrence depends on opposing effects of glycinergic and GABAergic inhibition

63 Similarly, we demonstrated opposing effects of GRK2 and -6 on IGF-1R degradation: G

64 We also show how opposing effects of group size directly and indirectly a

65 f virus adaptation that incorporates the two opposing effects of host immunity on the virus populatio

66 r growth; rather, we found only additive and opposing effects of hypoxia (detrimental) and warming (b

67 However, opposing effects of IL-6 have been observed in models of

68 use transplantation models, possibly through opposing effects of increased TGF-beta1 on the respectiv

69 ntent for high fat nanoemulsions, due to the opposing effects of lipid digestion and micelle solubili

70 a novel epigenetic mechanism that underlies opposing effects of MLL4 and PRMT7 on cellular different

71 We report opposing effects of MMnet genes on bone mass in mice and

72 We find opposing effects of modernization on both sexual risk-ta

73 Rb1 pathway status then dictates the opposing effects of mutant Ras on the ZEB1-miR-200 loop

74 Our results also call attention to potential opposing effects of NMDAR antagonists as a treatment for

75 This study clarifies the opposing effects of Norrin on glioblastoma tumor growth

76 The opposing effects of ORC1 and CDC6 in controlling the lev

77 Taken together with the opposing effects of Pax3 and Tcof1 on NCC differentiatio

78 als of DG compared with CA1 PCs underlie the opposing effects of perisomatic GABAergic transmission.

79 More importantly, the opposing effects of PPARdelta and PPARgamma in regulatin

80 ersible arginine methylation of TRAF6 by the opposing effects of PRMT1 and JMJD6 is, therefore, a nov

81 nsistent with separate binding sites for the opposing effects of propofol.

82 Intriguingly, opposing effects of RCANs in both cell types were shown

83 C57BL/6 mice showed opposing effects of S1P(2) and EP(4) receptor activation

84 ponses to warming requires disentangling the opposing effects of selection and gene flow.

85 1)-GATA2, and nuclear GATA2, which links the opposing effects of serine and tyrosine phosphorylations

86 The opposing effects of serotonin, mediated by distinct 5-HT

87 The opposing effects of Shadoo in different model systems re

88 ing a Nanog-GFP reporter line, we discovered opposing effects of Snai1 and Snai2 depletion on Nanog p

89 is temporally and spatially modulated by the opposing effects of specific phosphoinositide-metabolizi

90 Here, we review findings that suggest that opposing effects of stress and/or depression and antidep

91 These genetic data are paralleled by opposing effects of Sui(-) and Ssu(-) substitutions on t

92 indings confirm and extend prior data on the opposing effects of the APOE epsilon4 and epsilon2 allel

93 conditions is to find a balance between two opposing effects of the carboxylic acid in the reaction

94 incoherent feedforward is implemented by the opposing effects of the domain size on the rate and dura

95 The opposing effects of the inhibitors cocaine and ibogaine

96 The opposing effects of the kallikrein-kinin system are medi

97 interactions have been described, we report opposing effects of the same galectin family member on a

98 Together, these findings reveal distinct and opposing effects of the T cell costimulatory pathway and

99 tion and increases nNOS protein, showing the opposing effects of the two chaperones as they participa

100 Together our data reveal global and opposing effects of the two most common cytosine modific

101 To elucidate a mechanism for the opposing effects of these HLA alleles on PBC susceptibil

102 Understanding the opposing effects of these mediators is difficult due to

103 Underscoring the opposing effects of Tia1 deletion and low SMN level on B

104 These opposing effects of tissue omega-6 and omega-3 fatty aci

105 This work revealed opposing effects of TLR9 and TLR3, TLR4, and TLR7 on the

106 ment can indeed be obtained by balancing the opposing effects of varying the ratio and by carefully a

107 C-Ar or N-Ar rings, which is ascribed to the opposing effect on metal-ligand sigma- and pai-bonding.

108 The opposing effect on survival of Rb-deficient alpha- and b

109 harmacological experiments revealed that the opposing effect on these neurons is mediated by the acti

110 Bacitracin caused an unusual time-dependent opposing effect on viral infection.

111 se two post-translational modifications have opposing effects on 4.1N association with GluK2 kainate

112 that TGF-beta exerts distinct and sometimes opposing effects on a disease progression depending on t

113 d glycinergic antagonists in the BotC caused opposing effects on abdominal expiratory activity, sugge

114 iency for the microglial CX3CR1 receptor has opposing effects on Abeta and MAPT pathologies.

115 We demonstrate that TREM2 deficiency has opposing effects on AD-related pathologies at early and

116 , we conclude that miR-221 and miR-130a have opposing effects on airway and vascular morphogenesis of

117 2-AG signaling in the ventral MHb and led to opposing effects on anxiety- and depressive-like behavio

118 We found that ARAP2 and ACAP1 had opposing effects on apparent integrin beta1 internalizat

119 d secondary thiol metabolic routes by having opposing effects on APSK and APS reductase in plants.

120 ing plk4 and slimb mutations, balances their opposing effects on Asl reduction, restoring seemingly n

121 eviously unreported pleiotropic alleles with opposing effects on atopic dermatitis and psoriasis risk

122 The opposing effects on atopy vs. non-atopic asthma might be

123 In mice, ANP and mANP (10-100 nmol/L) had opposing effects on atrial myocyte AP morphology and ICa

124 frequently mutated in human cancers and has opposing effects on autophagy and tumorigenesis.

125 Surprisingly, the opposing effects on background and evoked currents could

126 ecies in the MOM-mimicking vesicles can have opposing effects on Bax pore formation.

127 We hypothesize that UVR has opposing effects on BCC carcinogenesis-stimulatory via m

128 guished by their projection fields and their opposing effects on behavior.

129 relationship is likely to be complex due to opposing effects on behaviour and metabolism.

130 teolytically processed to isoforms that have opposing effects on beta-catenin activity.

131 and IFNgamma each have distinct and in part opposing effects on beta-cell TXNIP expression.

132 nin B2, two G protein-coupled receptors with opposing effects on blood vessel constriction, triggers

133 we unexpectedly found that tsl and tor have opposing effects on body size; tsl null mutants are smal

134 Avpr1alpha) and the Oxt receptor (Oxtr) have opposing effects on bone mass: Oxtr(-/-) mice have osteo

135 rane and soluble isoforms have diametrically opposing effects on both tumor growth and myeloid conten

136 few hundred neurons, that exert powerful and opposing effects on breathing.

137 he mechanism by which CPEB2 isoforms mediate opposing effects on cancer-related phenotypes, we used n

138 Two metabolomics QTL hotspots had opposing effects on carbon and nitrogen rich metabolites

139 Different cAMP pools have opposing effects on cardiac myocyte cell size.

140 iomyocyte numbers during development through opposing effects on cardiomyocyte proliferation mediated

141 Rac and Rho GTPases exert opposing effects on cell morphology and are stimulated d

142 late cell growth and proliferation, but have opposing effects on cell survival.

143 However, they often have opposing effects on cell-fate decisions with each pathwa

144 y homologous HSP70s, HSPA1A and HSPA1L, have opposing effects on cellular handling of various substra

145 tely regulates phenotypic modulation through opposing effects on chromatin accessibility at the promo

146 utonomously, such as tau, exhibit surprising opposing effects on circuit dynamics.

147 tion and plasticity in E. vaginatum thus had opposing effects on CO(2) fluxes, suggesting that warmin

148 ly-similar large PG, has different and often opposing effects on collagen.

149 osphorylation of activated PKCalpha but have opposing effects on degradation of the phosphorylated pr

150 modulate pathways important in CR may exert opposing effects on different cell types.

151 ates that dopamine (0.1-10 mm) exerts novel, opposing effects on different populations of mammalian (

152 itative variation may impose diverse or even opposing effects on distinct lineages of T cells, an opt

153 chondrial PKA scaffold AKAP1, apparently via opposing effects on Drp1 S637 phosphorylation.

154 sease stage, CD47 has Janus-like roles, with opposing effects on EAE pathogenesis.

155 nd non-canonical Wnt/Frizzled signaling have opposing effects on ECM organization underlying PCP and

156 s suggested that canonical Wnt signaling has opposing effects on epidermal and hair follicle stem cel

157 Furthermore, each factor has opposing effects on established neurogenic genes Neurog2

158 at CRF1 and CRF2 receptors in the BNSTAL had opposing effects on exploratory behavior in the elevated

159 lopment comprising biological processes with opposing effects on FA, such as axonal myelination and p

160 hat dorsal and ventral mPFC subregions exert opposing effects on fear, as do subregions of other stru

161 y did not colocalize with each other and had opposing effects on focal adhesions (FAs).

162 m the same hypothalamic progenitors but have opposing effects on food intake.

163 ation and trans-SNARE complex zippering have opposing effects on fragment formation and verify that t

164 when the involved transcription factors have opposing effects on gene regulation, like P53 tumor supp

165 criptional regulators Slx and Sly [3-7] have opposing effects on global transcription levels of the s

166 ntial signal for axon guidance that mediates opposing effects on growth cone motility.

167 cellular sites and inducers of ROS can have opposing effects on GSIS, perhaps explaining some of the

168 Frizzled6 receptors act in parallel and have opposing effects on hair cell PCP.

169 s in maternal care in the rat associate with opposing effects on hippocampal function in the dorsal a

170 Adult-onset stressors exert opposing effects on hippocampal neurogenesis and cogniti

171 enal glucocorticoid secretion, but they have opposing effects on hippocampal neurogenesis and mood.

172 s and proteins with varied, overlapping, and opposing effects on histological and behavioral recovery

173 onists (PA452 and HX531) had independent and opposing effects on I (Ca) that were also time-dependent

174 ANP and mANP also had opposing effects on ICa,L in human atrial myocytes.

175 Here, we identified opposing effects on ILCs by two Helicobacter species, He

176 ions by phosphorylation and methylation have opposing effects on in vitro translational regulation, w

177 olymorphisms (SNPs) previously found to have opposing effects on infant erythrocyte DHA.

178 p35 is common to IL-35 and IL-12, which have opposing effects on inflammation.

179 uing insight that obestatin and ghrelin have opposing effects on insulin secretion, and both are medi

180 stria terminalis, and these projections have opposing effects on investigation or avoidance of threat

181 An EDNRA locus demonstrated opposing effects on ischemic and hemorrhagic stroke.

182 e for binding to the Lmo3 promoter and exert opposing effects on its transcription; repressing Lmo3 b

183 triatonigral and striatopallidal neurons has opposing effects on LID.

184 Stressors combined additively, but had opposing effects on life history tactics: migration incr

185 Modulating PGE2 activity has opposing effects on liver versus pancreas specification

186 Street canopy exerted opposing effects on loading, where elevated nutrient con

187 ation of PPN cholinergic cell bodies exerted opposing effects on locomotor behavior and reinforcement

188 Thus, cAMP-downregulation by CIRL exerts opposing effects on low-threshold mechanosensors and hig

189 NO and oxidative modifications have opposing effects on M-current, suggesting that a tightly

190 -surface and secreted isoforms of CSF-1 have opposing effects on macrophage activation and disease pr

191 tic selection--where alleles at a locus have opposing effects on male and female fitness ("sexual ant

192 The IgAN risk alleles have opposing effects on many immune-mediated diseases, sugge

193 nt downstream basal ganglia targets and have opposing effects on motivated behavior, yet differential

194 onclusion, vitamin A and D deficiencies have opposing effects on mouse survival from BCR-ABL ALL.

195 so-called direct and indirect pathways--have opposing effects on movement: activity of direct-pathway

196 IF17-Tail decreased the K0.5MT of K370, with opposing effects on MT-stimulated ATPase activity.

197 HIV infection and ART have opposing effects on mtDNA content in adipose tissue; imm

198 and CDC42b in neurogenesis are due to their opposing effects on mTORC1 activity.

199 HD-ZIPIII transcription factor REVOLUTA has opposing effects on multiple components of the auxin pat

200 Bmp signaling exerts opposing effects on myocardial differentiation in the em

201 nd modularity (how a group is clustered) had opposing effects on network efficiency, showing that tol

202 of synaptic and intrinsic conductances with opposing effects on neuronal activity when temperature c

203 machinery and an F-box protein, MEC-15, have opposing effects on neuronal differentiation, and that t

204 in which highly similar molecules may exert opposing effects on neurons.

205 The two forms have opposing effects on neurons: NGF induces proliferation,

206 omote androgen-independent cell survival via opposing effects on NF-kappaB and p53 function.

207 Thus, galectin-1 can have dual and opposing effects on NiV infection of human endothelial c

208 vide evidence that endocannabinoids can have opposing effects on nociceptive vs. non-nociceptive path

209 postmeiotic sex chromatin (PMSC) [8-11] and opposing effects on offspring sex ratio.

210 that exogenous and endogenous serotonin have opposing effects on olfactory responses.

211 ific niches has been implicated in mediating opposing effects on organotropic metastasis to the lungs

212 L-1alpha and IFNbeta, cytokines that exhibit opposing effects on osteoclast formation.

213 pression of some genes and apparently having opposing effects on others.

214 icient alpha- and beta-cells was a result of opposing effects on p53 in these cell types.

215 current MRI) had highly significant (p<0.01) opposing effects on pain scores (std.

216 current MRI) had highly significant (p<0.01) opposing effects on pain scores (std. beta=-0.46 and 0.4

217 illustrating that a single factor may exert opposing effects on pathogenesis in distinct host niches

218 ified sORF2 as a key regulatory element with opposing effects on PB1-F2 and PB1-N40 expression.

219 Our data thus show that FcgammaRIIb has opposing effects on pre-immune and post-immune tolerance

220 Intragenic 5-methylcytosine and CTCF mediate opposing effects on pre-mRNA splicing: CTCF promotes inc

221 ish models of these syndromes, we identified opposing effects on production of beta-cells.

222 Moreover, loss of myosin II activity has opposing effects on protrusive activity in fibroblasts o

223 nce of macronutrients has marked and largely opposing effects on reproductive and longevity outcomes.

224 Opposing effects on RF rates were also observed in growt

225 uption of the MBD only or the entire CTT had opposing effects on ribosome binding, substrate-protein

226 t RfaH and exit channel duplexes compete via opposing effects on RNAP clamp conformation.

227 nosteroid (BR) hormone is shown here to have opposing effects on root meristem size, depending on its

228 Despite having opposing effects on ROS levels, loss of TIGAR and RAC1 c

229 erated by TNF-releasing disease processes by opposing effects on ryanodine channels.

230 nterneurons in the dorsal striatum and exert opposing effects on sensory-guided behavior.

231 lations demonstrate that N addition can have opposing effects on separate soil C pools (particulate a

232 FtsZ filaments and lipid membranes have opposing effects on SepF polymerization, indicating that

233 apted and nonassociated polymorphisms showed opposing effects on set-point VL and the balance between

234 c Ca(V)2.1 channels by CaBP1 and VILIP-2 has opposing effects on short-term synaptic plasticity in su

235 gs to bind smad1 RNA, Rpl22 and Rpl22l1 have opposing effects on Smad1 expression.

236 Fgfr3(K650E) had opposing effects on Sox9 and beta-catenin protein stabil

237 utants, we show that SCF(Cdc4) and Ubp3 have opposing effects on Ste7 ubiquitination.

238 in the stability of Glut4 mRNA, resulting in opposing effects on steady-state Glut4 mRNA levels.

239 structures reveal how each disulfide exerts opposing effects on structure and function.

240 101) are highly homologous alleles that have opposing effects on susceptibility to primary biliary ci

241 ntaining proteins in hippocampal neurons has opposing effects on synaptic strength, decreasing and in

242 lpha2, which differ in their C-termini, have opposing effects on synaptic strength.

243 ms of p38 activation converge on NFATc1 with opposing effects on T cell immunity, which may underlie

244 ion by the snail intermediate hosts, causing opposing effects on tadpole per capita exposure to trema

245 logous variants in the Hsp70 family can have opposing effects on tau clearance kinetics.

246 two TbetaRI-interacting regions (TIRs) with opposing effects on TGF-beta signaling.

247 subunits, the two phosphorylation sites have opposing effects on the ability of each hexamer to bind

248 TLR4 and caveolin-1 exert opposing effects on the activation of ERK1/2, PI3-K and

249 Ai-mediated suppression of PTP1B resulted in opposing effects on the activity of BRK and SRC and have

250 In vitro, the flanking domains have opposing effects on the conformation and stabilities of

251 tion and/or overexpression of miR-511-3p has opposing effects on the expression levels of two key C-t

252 As a result, vHMM-HA and HMM-HA induce opposing effects on the expression of CD44-dependent gen

253 phosphatases, Ppn1 and Ppn2, that could have opposing effects on the extent of K-PPn.

254 y or circulating inflammatory cells can have opposing effects on the generation of inflammatory media

255 at individual G186V and L194P mutations have opposing effects on the HA receptor-binding site (RBS),

256 Localization of AGR2 also has opposing effects on the Hippo pathway, spheroid formatio

257 How these two opposing effects on the host may be modulated in future

258 Mutations in this loop promote opposing effects on the natural equilibrium between thes

259 The T4A and S7A mutations had opposing effects on the phosphate response pathway.

260 Changing the ionic environment has opposing effects on the propensity for heterotypic pepti

261 effects depending on sex, but also can have opposing effects on the same tissue: across both species

262 is a regulator of liver fat metabolism with opposing effects on the secretion of TRLs and hepatic li

263 dramatically in different contexts and have opposing effects on the selection for non-cooperating ch

264 Hence, TSPY and TSPX exert opposing effects on the transactivation functions of AR

265 Fgf and Wnt, the two pathways generally have opposing effects on the transcription of co-regulated ge

266 Differing and sometimes opposing effects on the Treg compartment have been obser

267 The opposing effects on the two receptor forms thus led to a

268 tion by the 5'->3' exonuclease Xrn1 to enact opposing effects on the UPR.

269 mote or attenuate tumorigenesis and can have opposing effects on therapeutic outcome.

270 Specific eicosanoid receptors had opposing effects on TLR3 activator-induced GDNF expressi

271 ct that targeted pathway modulators may have opposing effects on tolerance based on their impact on e

272 The two microRNAs had opposing effects on transcriptional heterogeneity within

273 Therefore, FOS and FOSL1 exert opposing effects on trophoblast invasion.

274 However, they exert opposing effects on TRPM8 gating properties.

275 Recombinant MIF exerted opposing effects on tubular cells in vitro and in vivo O

276 -2 and VEGFR-1 blocking antibodies displayed opposing effects on tumor angiogenesis.

277 factor (VEGF) and Ang1 (Angiopoietin-1) have opposing effects on vascular permeability, but the molec

278 rved ejection fraction, sildenafil displayed opposing effects on ventricular and vascular function.

279 r phosphaturic hormones, PTH and FGF23, have opposing effects on vitamin D production, placing vitami

280 It exerts opposing effects on vocalization in nocturnal versus diu

281 mperatures and decreasing winter length have opposing effects on Wood Frog winter energy requirements

282 Drosophila Rtca and Archease had opposing effects on Xbp1 splicing, and deficiency of Arc

283 asion, metastasis, and vascularization, with opposing effects produced by ROBO1 silencing in tumor ce

284 e dysregulated, will lead to different, even opposing effects, producing prenatal as well as later ne

285 al populations and neuro-mediators can exert opposing effects, promoting or inhibiting tissue immunit

286 Computational modelling suggests that these opposing effects reflect a fast-slow timescale hierarchy

287 ic roles, yet the mechanisms underlying such opposing effects remain unclear.

288 larification of the mechanisms causing these opposing effects should provide a better guide for thera

289 mal ploidy (aneuploidy) can have a number of opposing effects, such as unbalancing protein abundances

290 Variants in the TOM1L2/SREBF1 locus exert opposing effects TB-LM and TBLH-BMD, and have a stronger

291 results from a delicate balance between two opposing effects: the loss of conformational entropy due

292 d by the interplay between two currents with opposing effects: the rapid delayed rectifier potassium

293 The combination of the two opposing effects thus results in nearly identical overal

294 have elevated epoxy-oxylipins, demonstrated opposing effects to epoxI-treated mice: reduced Ly6c(hi)

295 Thus, MIC-1 displays two opposing effects: tumor suppression versus promotion.

296 aride A-deficient BF failed to produce these opposing effects upon oral and systemic deliveries.

297 ization by Ral downstream pathways, based on opposing effects via the Ral effectors RalBP1 and phosph

298 The opposing effect was observed during generation of MSCs f

299 ellular actions of IL-2, its cooperative and opposing effects with other cytokines, and how both prom

300 ive processes that may have distinct or even opposing effects with respect to insulin sensitivity.