ライフサイエンスコーパス: opposing effect

1 le other cytoplasmic domains had a competing opposing effect.

2 larified how the same receptor mediates such opposing effects.

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

4 having profibrotic effects and others having opposing effects.

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

6 colon adenocarcinomas, consistent with their opposing effects.

7 differentiation, whereas overexpression has opposing effects.

8 should be carefully tested in vivo for such opposing effects.

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

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

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

12 an antisense selective against nNOS-2 had an opposing effect against the first phase, increasing its

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

14 e mechanisms that selectively regulate these opposing effects are not yet fully understood.

15 These opposing effects are suited to prevent premature cleavag

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

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

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

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

20 and temporally regulated phosphorylation has opposing effects directly on overt circadian rhythms and

21 n assays where anosmin-1 was shown to induce opposing effects during chemotaxis of human neuronal cel

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

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

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

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

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

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

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

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

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

31 rms, 43-kilodaltons and 40-kilodaltons, have opposing effects in apoptosis.

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

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

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

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

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

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

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 These two opposing effects lead to robust adaptation toward stimul

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

42 e find that the two residues have strong and opposing effects: N richness promotes assembly of benign

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

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

45 .58; 95% CI, 0.35 to 0.94) was masked by the opposing effect of its member allele B*1510.

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

47 The opposing effect of TGFbeta on CCN2 and CCN3 expression a

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

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

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

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

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

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

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

55 The opposing effects of C3a and C5a were mediated through th

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

57 How cells quantitatively reconcile the opposing effects of cell-cell contact and GFs, such as e

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

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

60 The opposing effects of Cut and Slbo in these two tissues re

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

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

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

64 evance of these findings is supported by the opposing effects of Flightless-I overexpression and knoc

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

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

67 sttranslational histone modifications on the opposing effects of glucose and cAMP on the L-PK gene is

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

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

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

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

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

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

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

75 Similar opposing effects of linguistic and visual primes were al

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

91 The opposing effects of Shadoo in different model systems re

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

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

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

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

96 immune responses are finely regulated by the opposing effects of Th17 and T regulatory (Treg) cells.

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

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

99 The opposing effects of the inhibitors cocaine and ibogaine

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

101 Our lab has found opposing effects of the monoamine oxidase inhibitor phen

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

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

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

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

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

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

108 nded framework for understanding the roughly opposing effects of these motility regulators.

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

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

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

112 issue of Immunity, Yagi et al. describe the opposing effects of transcription factors Runx3 and GATA

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

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

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

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

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

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

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

120 Although insulin and metformin display opposing effects on Abeta generation, in combined use, m

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

122 n the frequency of the original host has two opposing effects on adaptation: an increase in the suppl

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

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

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

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

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

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

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

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

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

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

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

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

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

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

137 The two mutants also had opposing effects on binding of aa-tRNA to the ribosomal

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

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

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

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

142 equence, through which vigilin and HuR exert opposing effects on c-fms expression, suggesting a role

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

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

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

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

147 f ARNO/cytohesin 2 and GRP1/cytohesin 3 have opposing effects on cell adhesion and spreading on fibro

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

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

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

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

152 miR-125b and miR-132 had largely opposing effects on dendritic spine morphology and synap

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

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

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

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

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

158 and miR-200 are mutually inhibitory and have opposing effects on EMT and metastasis.

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

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

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

162 ies influence bioavailability with typically opposing effects on Fa and first-pass elimination.

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

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

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

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

167 smic poly(A) binding protein (PABPC) to have opposing effects on gene expression when concentrated in

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

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

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

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

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

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

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

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

176 find that BMPR1a and BMPR1b signaling exerts opposing effects on hypertrophy.

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

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

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

180 terning receptor expression were linked with opposing effects on inflammatory, procatabolic responses

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

182 ellular triglycerides (IMTGs) despite having opposing effects on insulin sensitivity.

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

184 triatonigral and striatopallidal neurons has opposing effects on LID.

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

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

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

191 ing by only 16 amino acids, exhibit markedly opposing effects on mammary epithelium growth and differ

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

193 MitoPLD and Lipin 1 have opposing effects on mitochondria length and on intermito

194 in which a ligand-receptor system generates opposing effects on mitogenesis by differentially regula

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

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

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

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

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

200 vitro findings, fimbrin and tropomyosin have opposing effects on Myo1p function at actin patches.

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

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

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

204 ead to a model where proteoglycans can exert opposing effects on neuronal extension by competing to c

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

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

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

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

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

210 ystemic injections, D1 and D2 receptors have opposing effects on odor discrimination learning.

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

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 RA and epidermal growth factor had opposing effects on phosphorylation of CBP by extracellu

220 Thus, eLNs have two opposing effects on PNs, driving both direct excitation

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

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

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

224 TNFR1 and TNFR2 have disparate and opposing effects on remodeling, hypertrophy, NF-kappaB,

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

226 Opposing effects on RF rates were also observed in growt

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

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

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

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

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

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

233 results suggest that neurotrophins can exert opposing effects on SG neurons, the balance of competing

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 The two optoXRs exerted opposing effects on spike firing in nucleus accumbens in

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

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

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 mediated CARMA1 phosphorylation events exert opposing effects on the activation status of CARMA1.

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

251 compete for the same binding site, but have opposing effects on the activity of the receptor protein

252 -DeltaN100 and cTnT3-DeltaE101 mutations had opposing effects on the Ca(2+) sensitivity of force deve

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

254 ligand Dll4 activate neural precursors with opposing effects on the density of blood vessels.

255 ow that TrkA and p75 signaling pathways have opposing effects on the firing properties of sympathetic

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

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

258 dicate that BMPR1a and BMPR1b exert directly opposing effects on the initial reactive astrocytic hype

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

260 They appear to have opposing effects on the nucleosome, H1 stabilising it by

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

262 We find that the two receptors exert opposing effects on the posttranscriptional regulation o

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

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

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

266 opose that calcium and d-serine binding have opposing effects on the stability of the dimer interface

267 s mRNA, and changes in -1 RF efficiency have opposing effects on the steady-state abundance of the ES

268 y between, at least, two processes that have opposing effects on the tension output as the shortening

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

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

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

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

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

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

275 The two microRNAs had opposing effects on transcriptional heterogeneity within

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

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

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

279 -2 and VEGFR-1 blocking antibodies displayed opposing effects on tumor angiogenesis.

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

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

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

283 It exerts opposing effects on vocalization in nocturnal versus diu

284 ted MLCP, the ROCK isoforms had distinct and opposing effects on VSMC morphology and ROCK2, but not R

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

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

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

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

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

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 nctionally divergent T cell subsets can have opposing effects -- they can trigger tumor rejection or

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 Dyslipidemia thus imparts opposing effects upon intra- and extrapulmonary host def

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

298 Opposing effects were produced by central infusions of m

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.