ライフサイエンスコーパス: antagonism

1 eractors, which can mediate their functional antagonism.

2 nized transition state between mutualism and antagonism.

3 servatism, cultural conservatism, and ethnic antagonism.

4 is suggested by its ability to overcome VEGF antagonism.

5 by systemic or SNr-localized 5-HT2C receptor antagonism.

6 ential selective advantage aside from sexual antagonism.

7 ortive of more recent studies that find more antagonism.

8 HIV-1 infection is reduced by P2X1 receptor antagonism.

9 ike activity has been attributed to the Ser5 antagonism.

10 on effects including synergy, additivity and antagonism.

11 these phenotypes are reversed following KOR antagonism.

12 interpretation of in vivo responses to CCR2 antagonism.

13 antimicrobial molecules or through signaling antagonism.

14 le sequence differences for subtype-specific antagonism.

15 n, and N-methyl-D-aspartate receptor, NMDAR, antagonism.

16 omain (FSD) important for ligand binding and antagonism.

17 e to the human intruder threat after 5HT(2A) antagonism.

18 nome-wide association study (GWAS) of sexual antagonism.

19 hibited enhancement, some mixtures exhibited antagonism.

20 hin the domain that are important for ligand antagonism.

21 me3 are maintained in that state by H3K36me3 antagonism.

22 gh-order combinations by strength of synergy/antagonism.

23 saccharides is of critical importance in the antagonism.

24 etion led to a partial rescue from oncogenic antagonism.

25 ependent of S7 phosphorylation and NF-kappaB antagonism.

26 he ubiquity and importance of interbacterial antagonism.

27 -mediated intra- and inter-species bacterial antagonism.

28 protein interactions required for potent A3 antagonism.

29 1)R, conveying a longer duration of receptor antagonism.

30 AT1 and the greatest reduction in interferon antagonism.

31 y inhibits CaSR activity via non-competitive antagonism.

32 ng the selectivity as well as agonism versus antagonism.

33 ssue tropism, viral pathogenesis, and immune antagonism.

34 ter to the long-standing pursuit of glucagon antagonism.

35 also be reversed by systemic 5-HT2C receptor antagonism.

36 nd pan-antagonists that exert broad-scope AR antagonism.

37 hat mediate contact-dependent interbacterial antagonism(1-3).

38 , as expected from the addition of sigma(1)R antagonism, 15au showed local, peripheral activity in th

39 t RNA sequencing analysis suggests that VEGF antagonism activates retinal degeneration, inflammation,

40 ith an EC(50) of 7.2 uM and no detectable PR antagonism activity.

41 ltered colony and cell morphology, motility, antagonism against other microbes, and biofilm formation

42 Additional evidence for this mechanism of antagonism also comes from monitoring the reduction of p

43 CB1R antagonism also inhibited memory retrieval-associated in

44 rs, suggesting that pharmacologic purinergic antagonism, altering the innate and adaptive immune comp

45 relapse, we evaluated whether systemic CB1R antagonism (AM251; 3 mg/kg, i.p.) during memory reconsol

46 (EST73502) showed MOR agonism and sigma(1)R antagonism and a potent analgesic activity, comparable t

47 two-stressor combinations, we conclude that antagonism and additivity are the most frequent interact

48 gainst in vitro active concentrations for AR antagonism and androgen synthesis suppression.

49 sly undescribed mechanism for interbacterial antagonism and demonstrate a physiological role for the

50 t-regulated molecules show potent beta(2)-AR antagonism and enable a reversible and dynamic control o

51 several signature feedbacks behind the M1-M2 antagonism and investigated the dynamical shaping of mac

52 coevolution in nature occurs in networks of antagonism and mutualism.

53 mulsion polyplexes to achieve combined CXCR4 antagonism and PAI-1 inhibition is a promising strategy

54 tion to II and III produced submicromolar AR antagonism and protein degradation selective to AR and A

55 or disentangling the effects of evolutionary antagonism and suppressed recombination.

56 story traits, yet their mechanism of action, antagonism and targets remain poorly understood.

57 e a comprehensive structural basis of NK(1)R antagonism and will facilitate the design of new therape

58 ed dual profile (i.e., MOR agonism and sigma antagonism) and a potent analgesic activity, comparable

59 and MYC goes further, beyond transcriptional antagonism, and governs a multitude of developmental pat

60 re generally, suggest consideration of BCL-2 antagonism as a means of enhancing CTL immunotherapy in

61 n patients with AD, confirming H(4) receptor antagonism as a novel therapeutic option.

62 cy and safety margin strongly validates PAR4 antagonism as a promising antithrombotic mechanism.

63 in epithelial cell-death, and support CDKL5 antagonism as a therapeutic approach for AKI.

64 linical isolates is positively influenced in antagonism assays against S. mutans.

65 shed light on pathogenic mechanisms for VEGF antagonism-associated adverse effects and potential ther

66 To study mechanisms for VEGF antagonism-associated adverse effects in visual system,

67 mitigated by normalizing mechanisms such as antagonism at the level of receptor-ligand interactions,

68 R-Ab-associated AE patients and simultaneous antagonism at the NMDAR by AP5, particularly in burst ac

69 sensory neurons, and we find that that CXCR3 antagonism attenuates chronic itch.

70 nctional studies reveal that PX exploits the antagonism between beta-arrestin isoforms; in low ligand

71 A functional antagonism between Ddr/Intbeta1-mediated cell-matrix adh

72 We provide evidence that the antagonism between FT and TFL1 relies on competition for

73 Our work uncovers a mutual antagonism between Gli3 and Hox13 paralogs that has impo

74 other Hsp90 substrates, is fine-tuned by the antagonism between MEC-15 and the chaperones; this antag

75 rected repair of DSBs is delayed, indicating antagonism between nuclear migration and the mechanism o

76 The apparent antagonism between salicylic acid (SA) and jasmonic acid

77 ibitor treatment modes, we tested synergy or antagonism between several inhibitors with tungstate, an

78 Antagonism between SNORD50A/B RNAs and specific SNARE pr

79 nature of adaptive responses to evolutionary antagonism between social forms.

80 This mutual antagonism between STRIPAK and SAV1 controls the initiat

81 In the present study, we investigate the antagonism between the microbiota and Klebsiella pneumon

82 In many cells, polarity involves mutual antagonism between the Par complex and the Scribble (Scr

83 ls and verify the occurrence of synergism or antagonism between them.

84 lls with the ability to mitigate an inherent antagonism between transcription and DNA replication.

85 id cation channels (TRPVs) since TRPV1/TRPV4 antagonism blocked the febrile Th2 switch, while TRPV1 a

86 une myeloid cells and show that systemic EP2 antagonism blocks monocyte brain entry in male mice.

87 trast, reversal learning was impaired by D2R antagonism, but not D1R antagonism, in the dorsal striat

88 lization of contact-dependent interbacterial antagonism by AID systems helps to shape human gut micro

89 tigated protease-activated receptor 4 (PAR4) antagonism by developing and evaluating a tool compound,

90 ological inhibition of CypA rescues PKR from antagonism by HCV NS5A, leading to activation of an inte

91 nonetheless provides relative resistance to antagonism by HIV-1 Nef.

92 cellular restriction factor APOBEC3G and its antagonism by HIV-1 Vif has underpinned two decades of r

93 ast, effector T cells responded to glutamine antagonism by markedly up-regulating oxidative metabolis

94 nal, increases the sensitivity of SERINC5 to antagonism by Nef, while it has no effect on the intrins

95 these findings identify STAT5 as a target of antagonism by specific pathogenic flaviviruses to subver

96 these findings identify STAT5 as a target of antagonism by specific pathogenic flaviviruses to subver

97 d not increase the sensitivity of SERINC5 to antagonism by the glycoGag protein of MLV, suggesting th

98 Therefore, our results suggest that TRPV4 antagonism can attenuate aortic inflammation and remodel

99 The benefits of systemic EP2 antagonism can be attributed, in part, to blocking brain

100 Our observations indicate that P2X1 antagonism can inhibit HIV-1 replication at the level of

101 IL-17 receptor-A antagonism caused extensive improvements in clinical, hi

102 tative associations between thyroid receptor antagonism, chemical concentrations, and papillary thyro

103 on cancer cells, highlighting that UHRF1 SRA antagonism could be a cancer therapeutic strategy.

104 In this context, P2X7 receptor antagonism could be a promising strategy to prevent or t

105 nse to exercise suggests that ET(A) receptor antagonism could be a therapeutic approach to improve bl

106 These data indicate that ET(A) receptor antagonism could be a viable therapeutic approach to imp

107 noprecipitation (CLIP) experiments and miRNA antagonism demonstrated that these alternative variants

108 high-level PE responses, implying that NMDAR antagonism disrupts the inference on abstract statistica

109 al deficits were prevented by CB(1) receptor antagonism during maternal exposure, showing that the CB

110 typed marmosets with responsivity to 5HT(2A) antagonism during the human intruder test of anxiety.

111 Systemic CB1R antagonism, during, but not after, cocaine-memory recons

112 ed CCR2 in primary sensory neurons, and CCR2 antagonism effectively reduced bone cancer pain.

113 the utility of our procedure to predict OxR1 antagonism efficacy and relapse propensity.

114 ale, sex, and political attitudes, is ethnic antagonism-especially concerns about the political power

115 further transdiagnostic investigation of KOR antagonism for anhedonia is warranted.

116 their amplification is driven by X versus Y antagonism for increased transmission, where sex chromos

117 the potential of kappa-opioid receptor (KOR) antagonism for treating anhedonia with a POM study deter

118 d inhibited HPA activity via non-competitive antagonism from two allosteric sites, by channeling the

119 ivatives of 1 by Trp turned Y(4)R agonism to antagonism, giving Y(4)R antagonists with pK(i) values <

120 TGF-beta1 pathway antagonism has been proposed for the treatment of dystro

121 The Myc-p27 antagonism has been shown to be relevant in human cancer

122 (cort) levels in rats, whereas central GLP1R antagonism has opposite effects.

123 in's antiviral activities and viral tetherin antagonism have been studied in detail for a number of d

124 tis (AD), but the molecular effects of IL-22 antagonism have not been defined in human subjects.

125 This antagonism helps pattern the mesoderm along the dorsoven

126 We found that systemic M(1) mAChR antagonism impaired contextual fear extinction.

127 ple characterized by elevated anhedonia, KOR antagonism improved the ability to modulate behavior as

128 Sustained GPR55 antagonism in 3T3-L1 adipocytes enhanced expression of p

129 of ER degradation does not guarantee full ER antagonism in breast cancer cells; ER "degraders" exhibi

130 on, raising the hypothesis that IL-6 pathway antagonism in CHIP carriers would decrease cardiovascula

131 n help determine significance of synergy and antagonism in drug combination screens with few data poi

132 nd was used in a bioassay to quantify TRbeta antagonism in human embryonic kidney cells (HEK293/17) a

133 e find that nonselective muscarinic receptor antagonism in mice as well as epithelial-specific ablati

134 Studies examining the role of antagonism in natural communities reveal it can serve ma

135 into the structural basis of agonism versus antagonism in steroid receptors with potential implicati

136 understanding selfish replication and sexual antagonism in the evolution of mitochondrial genomes and

137 h presynaptic inhibition, generating lateral antagonism in the orientation domain.

138 ehog activation signalling to upregulate BMP antagonism in the progenitor niche that promotes metapla

139 Recombinant virus (rAAV) leptin antagonism in the VTA decreased wheel running in standar

140 mal MN development raising caution about JNK antagonism in this pediatric neuromuscular disease.

141 gether our data unravel a mechanism of viral antagonism in which a virus hijacks the Nup98-Rae1 compl

142 ained by a shared genome, leading to 'sexual antagonism', in which different alleles at given loci ar

143 was impaired by D2R antagonism, but not D1R antagonism, in the dorsal striatum: raclopride increased

144 Furthermore, CB1R antagonism increased memory reconsolidation-associated s

145 distances, we found that the probability of antagonism increased the more metabolically similar the

146 Here, we confirmed that intraocular VEGF antagonism induced retinal degeneration and gliosis.

147 miR-25 and miR-124 overexpression, or let-7 antagonism, induced Ascl1 expression and conversion of ~

148 this bi-stable circuit of mutual cRel-Blimp1 antagonism into a multi-scale model revealed that dynami

149 Therefore, antagonism is a common feature of odor mixture encoding

150 We conclude that the antagonism is due to restricting the conformation of the

151 The antagonism is highly species specific because the amino

152 While APOBEC3 antagonism is the canonical function of HIV-1 Vif, this

153 inputs, yet their response to systemic NMDAR antagonism is unknown.

154 ET(A) receptor antagonism markedly increased leg blood flow, vascular c

155 evidence that dual MOR agonism and sigma(1)R antagonism may be a useful strategy for obtaining potent

156 evidence that dual MOR agonism and sigma(1)R antagonism may be a useful strategy for obtaining potent

157 ntific interest in the possibility that CGRP antagonism may disrupt vascular responses to CSD and the

158 se findings suggest that the amylin receptor antagonism may represent a novel therapy for AD.

159 Inhibition through a biased mode of antagonism might hold significant therapeutic promise by

160 ndent somites and challenge the T-Sox2 cross-antagonism model in early NMPs.

161 Specifically, let-7 and miR-148 antagonism modified PTH secretion in vivo and in vitro,

162 athology, and we observed that acute Adora2a antagonism normalized BBB permeability in wild-type mice

163 preserving perturbations - strength of cross-antagonism, number of operator sites in a promoter, and

164 In summary, we observed OR antagonism occurred frequently and in a combinatorial ma

165 nally, primed IFP-MSC demonstrated sustained antagonism of activated human peripheral blood mononucle

166 The antagonism of activation of TLRs and virus binding to th

167 mal phenotypes driven by ARID1A loss through antagonism of ARID1A target gene expression, resulting i

168 Consistent with this hypothesis, antagonism of AT1R using losartan or shRNA-mediated knoc

169 the LC-BLA pathway and intra-BLA or systemic antagonism of beta-adrenergic receptors abolished both l

170 We have previously demonstrated that antagonism of C-X-C chemokine receptor type 4 (CXCR4) by

171 Specifically, we evaluated TRbeta antagonism of chemical mixtures extracted from wristband

172 Intra-basolateral amygdala antagonism of dopamine D1-receptors did not prevent the

173 In fact, compound 38 exhibited potent antagonism of dopamine-stimulated beta-arrestin2 recruit

174 Antagonism of gamma-aminobutyric acid A receptors (GABA(

175 that, when substituted with alanine, reduce antagonism of GDF8 in full-length WFIKKN2.

176 behaviors were shown to be blocked by direct antagonism of GHSR(1a).

177 Antagonism of glycolysis also boosted EnAd replication a

178 ng to CRL4(DCAF1) E3, thereby disrupting Vpr antagonism of helicase-like transcription factor (HLTF)

179 Antagonism of host immune defenses against hepatitis B v

180 thiophenes resulted in potent and selective antagonism of human Complement C3a receptor.

181 f IFN-stimulated genes, which occurs through antagonism of IFN regulatory factor 1 (IRF1)-mediated tr

182 of patients with CRSwNP, demonstrating that antagonism of IL-4Ralpha signaling suppresses IL-4-/IL-1

183 se data identify a novel mechanism for viral antagonism of innate immune signaling which relies on se

184 A common flavivirus trait is the antagonism of interferon (IFN) signaling to enhance vira

185 Moreover, inhibition of S100a4 signaling via antagonism of its putative receptor, RAGE, also decrease

186 By contrast, antagonism of K(ATP) channels with glyburide significant

187 Depletion or antagonism of LPL suppressed human melanoma cell growth;

188 Therapeutic antagonism of MDM2 by small molecules and peptides in cl

189 , we identified and characterized type I IFN antagonism of MERS-CoV open reading frame (ORF) 8b acces

190 rkers for CA2, an effect mimicked by chronic antagonism of MRs.

191 independently of opioidergic mechanisms, as antagonism of mu-opioid receptors with systemically-admi

192 ary and sufficient for binding beta-TrCP and antagonism of NF-kappaB.

193 Antagonism of nicotinic acetylcholine receptors (nAChRs)

194 We observe that antagonism of NMDA and AMPA type glutamate receptors pro

195 the limited cognitive benefit of the direct antagonism of NMDA receptors in AD, we here focus on an

196 Pharmacologic antagonism of NMDARs in patients with depression may red

197 Intra-mPFC activation of NPY1R and antagonism of NPY2R resulted in decreased binge-like eth

198 Antagonism of PAFR amplified the inflammasome response b

199 reducing NO synthesis, and the knockdown or antagonism of PAI-1 increases NO bioavailability.

200 Antagonism of PP2A by HIV-1 Vif is therefore independent

201 These results highlight that the antagonism of Relish and Foxo functions are crucial in t

202 ted here offer significant insights into NS1 antagonism of RIG-I and illustrate the importance of und

203 ted negative sense RNA virus recognition and antagonism of RLRs.

204 Compared to Nef, the glycoGag antagonism of Ser5 is still poorly understood.

205 rify the mechanism underlying the functional antagonism of STAT2 by both ZIKV and DENV.

206 We envision the role of NOX proteins in the antagonism of T. guizhouense as an example of metabolic

207 As human tetherin lacks DIWK, antagonism of tetherin by Nef is a barrier to simian-hum

208 These data reveal antagonism of TGF-beta/SMAD3 activation by BMP signaling

209 roper morphogenesis, evoking the classic A-C antagonism of the ABC model for floral organ development

210 the mutually exclusive expression and cross-antagonism of the B cell identity factor Pax5 and the pl

211 model of PCa and associated fibroblast, the antagonism of the C3a receptor and the fibroblastic knoc

212 In contrast, antagonism of the common receptor for IL-13 and IL-4 by

213 Pharmacological antagonism of the cotransporter NKCC1 mitigated ethanol-

214 ion [MOI]) influences the magnitude of virus antagonism of the host innate antiviral response.

215 tantly, this was independent of Nef-mediated antagonism of the host restriction factor SERINC5.

216 egulating host signaling pathways, including antagonism of the innate immune response.

217 ammatory cytokine IL-1beta in the brain, and antagonism of the P2X7 receptor is a novel therapeutic s

218 tructure and displays potent, insurmountable antagonism of the Y(1) receptor.

219 cise in patients with hypertension via local antagonism of these receptors during exercise.

220 In this study, we identified RSV-mediated antagonism of this pathway, independent of the NS1 and N

221 Antagonism of TLR activation results in inhibition of th

222 hermore, genetic deficiency or pharmacologic antagonism of TRPV4 blocked cytokine-induced FBGC format

223 l sites of infection have been linked to the antagonism of type I IFN induction by N(pro) This protei

224 action with IRF3 is involved not only in its antagonism of type I IFN, but also dsRNA-mediated mitoch

225 e-tuned regulation of Ctgf through Hnf4alpha antagonism of Yap and Tgf-beta activities to balance reg

226 se C1s to evaluate the impact of upstream CP antagonism on activation and proliferation of normal and

227 a to investigate the putative effects of KOR antagonism on anhedonic behavior with more precision by

228 (BE) procedure to assess the effects of OxR1 antagonism on demand for the highly abused opioid fentan

229 t hydrolysis, opens channels when nucleotide antagonism on Kir6.2 is minimized and SUR1 mutants with

230 The corrosive impact of ethnic antagonism on Republicans' commitment to democracy under

231 l possible effects of NMDA receptor (NMDA-R) antagonism on this behaviour, we simulated the effects o

232 he tatM2NX C terminus are required to confer antagonism on TRPM2.

233 Antagonism or agonism of the glucose-dependent insulinot

234 ic (PD) approaches based on bioreceptor.drug antagonism or by pharmacokinetic (PK) approaches that se

235 Instead, many neurons exhibited either antagonism or enhancement of their response in the prese

236 ry human CD4 T cells and macrophages, whilst antagonism or genetic disruption of REV-ERB increased pr

237 te a reduced MAP response to VRS using TRPV1 antagonism or in Trpv1 null mice while the response to p

238 position to that produced by selective D(2)R antagonism or nonselective D(2)-like receptor antagonist

239 treatment, whereas local SNr 5-HT2C receptor antagonism or optogenetic activation of SNc DAergic neur

240 th, soil nutrient dynamics and interactions (antagonism or synergism) in a nutrient-poor greenhouse s

241 mechanical allodynia was attenuated by TLR9 antagonism or Tlr9 mutation only in male mice.

242 We posit that parental antagonism over embryonic growth drove the origin and on

243 The diversity and ubiquity of interbacterial antagonism pathways is becoming increasingly apparent, a

244 reviously undocumented phenomenon that P2Y1R antagonism patterns could vary in different signaling pa

245 ated by colony-stimulating factor 1 receptor antagonism (PLX5622) and allowed to repopulate, and resp

246 mera-type galectin-3 design makes functional antagonism possible, we underscore the value of versatil

247 Lastly, we find that 5-HT2C receptor antagonism potentiates the antidepressant and anxiolytic

248 our results demonstrate that selective D(3)R antagonism potentiates the behavioral-stimulant effects

249 Systemic EP2 antagonism prevented monocyte brain infiltration and pro

250 We found that CB2 antagonism prevented the development of ET and that bone

251 TGF-beta neutralization or receptor antagonism prevented the exacerbated neointimal formatio

252 sequence alignment to achieve a dual TLR7/8 antagonism profile and (ii) introduction of a fluorine i

253 Finally, TLR9 antagonism reduced paclitaxel-induced mechanical allodyn

254 Orexin-1 receptor (OxR1) antagonism reduces demand for cocaine and remifentanil,

255 ive capillary growth, suggesting that ligand antagonism regulates coronary primary plexus formation.

256 se VHL interacts with Daam2 and their mutual antagonism regulates oligodendrocyte differentiation dur

257 twork modeling indicates that VIP-SST mutual antagonism regulates the gain of the cortex to achieve s

258 nism between MEC-15 and the chaperones; this antagonism regulates TRN development, as well as synapti

259 BST-2, suggesting that the mechanism of this antagonism resembles that of HIV-1(NL4-3) Vpu against hu

260 Leukotriene receptor antagonism resulted in a significant reduction of early,

261 We found that, relative to placebo, KOR antagonism resulted in significantly higher learning rat

262 etR repression strength, which hinders cross-antagonism, resulted in a loss of mutually exclusive cel

263 for Setd1a and show that its pharmacological antagonism results in a full rescue of the behavioral an

264 ypothesize that gene degeneration and social antagonism shaped the evolution of the fire ant supergen

265 e, surprisingly little is known about how OR antagonism shapes neuronal representations in the detect

266 Consequently, antagonism should mostly be prevalent among phylogenetic

267 Significantly, Tnfa antagonism silenced the Cxcl8 pathway and decreased neut

268 Hence, it is conceivable that a functional antagonism strategy could lead to NP mitigation.

269 variant and by extension, suggest that a D3 antagonism strategy in substance use disorders should co

270 ficant advancement has been achieved in VEGF antagonism, substantial adverse effects have been report

271 ression with the same efficiency as IL-12p40 antagonism, suggesting that the efficacy of anti-IL-12p4

272 ntial effect on seizure susceptibility, TLR4 antagonism suppressed cellular inflammatory responses af

273 Strikingly, CP antagonism suppressed human Ig-induced activation of B c

274 Here we identify those effects of EP2 antagonism that are reproduced by conditional ablation o

275 al multipronged mechanisms of action of CD39 antagonism that rely not only on preventing the accumula

276 d euchromatin are globally poised for mutual antagonism, the mechanisms underlying precise spatial en

277 Glutamine antagonism therefore exposes a previously undefined diff

278 therapeutics due to its capacity for full ER antagonism, thought to be achieved through ER degradatio

279 AR variants, induced by AR antagonism to mediate resistance to AR pathway inhibitio

280 ls and underscore the potential of RORgammat antagonism to modulate aberrant type 17 responses.

281 up solidarity) and divisiveness (inter-group antagonism) to capture balance within and among subgroup

282 ll caged glutamates are known to have strong antagonism toward receptors of gamma-aminobutyric acid,

283 dark and Photoazolol-2 demonstrating higher antagonism upon illumination.

284 nexpected opposing functional profile of CB2 antagonism versus CB1 agonism.

285 d be blocked with systemic mGluR5 allosteric antagonism via MTEP.

286 A weak androgen receptor antagonism was identified, whereas no arylhydrocarbon re

287 the biphenyl carbamates 13m and 13n, neutral antagonism was observed for 14m and 14n and tiotropium u

288 Antagonism was positively associated with wristband conc

289 ased on the genetic evidence supporting GIPR antagonism, we previously developed a mouse anti-murine

290 Using nanobody-mediated ARTC2.2 antagonism, we showed that ARTC2.2 blockade enhanced NKT

291 ts during gastrulation induced by Hh pathway antagonism were mitigated by the addition of FGF4 protei

292 s are identified, including ADAM17 inhibitor antagonism when combined with PIK3CB/D inhibition contra

293 sex ratio, as well as conditions for sexual antagonism when mitochondrial variants increase transmis

294 human intruder after 5HT(2A) pharmacological antagonism, while CT/T/C individuals showed no effect.

295 cts in a common decision-making motif, cross-antagonism with autoregulation, by synthetically constru

296 little effects, but platelet P2Y12 receptor antagonism with clopidogrel, fibrinolysis with urokinase

297 cannabinoids, evidence of isolated vitamin K antagonism with or without bleeding, and detectable leve

298 aspirin-induced reactions, P2Y(12) receptor antagonism with prasugrel completely inhibited all aspir

299 t concentration exhibited significant TRbeta antagonism, with a mean of 30% and a range of 0-100%.

300 atly among opioids and it is unclear if OxR1 antagonism would reduce demand for all opioids, particul