ライフサイエンスコーパス: stimulator

1 d through increased amounts of ghrelin, a GH stimulator.

2 hile undergoing implantation of a deep brain stimulator.

3 urkholderia thailandensis, are potent immune stimulators.

4 hibitors of transcription into gene-specific stimulators.

5 sis of astrocytomas might be blocked by PKCe stimulators.

6 rease in CpG and UpA dinucleotides as immune stimulators.

7 human-use adjuvant ALFQ that contains immune-stimulators.

8 strikingly different effects depending on co-stimulators.

9 red engaged CD28, ICOS, CD226 and SLAM-F1 co-stimulators.

10 equired the adaptor protein IFNbeta promoter stimulator 1 (IPS-1, MAVS) and could be functionally unc

11 sing NS3/4A and TLR3/MyD88/IFN-beta promoter stimulator 1(-/-) mouse embryonic fibroblasts completely

12 ficiently cleaves TRIF and IFN-beta promoter stimulator 1, adaptors for TLR3 and the RLRs, respective

13 (PKC) pathways, while treatment with the PKC stimulator 12-O-tetradecanoylphorbol-13-acetate restored

14 One putative autophagy stimulator, 6-phosphofructo-2-kinase/fructose-2,6-biphos

15 of a biofuel cell (BFC) and an animal brain stimulator (ABS) implanted in a pigeon.

16 armacologic long-term treatment with a NO-GC stimulator altered auditory nerve responses but did not

17 igned for neurophysiological studies such as stimulators, amplifiers and recording microelectrodes do

18 hanocarba nucleosides (i.e., compound 3 as a stimulator and compound 8 as a partial inhibitor of P-gp

19 on between expression of inducible T-cell co-stimulator and induction of virus-specific antibodies in

20 lar basis for the mechanism of action of sGC stimulators and suggest the potential therapeutic utilit

21 The co-stimulators ICOS (inducible T cell co-stimulator) and CD28 are both important for T follicular

22 tivated transcutanously using a programmable stimulator, and the resultant finger flexion joint angle

23 al (pH, uric acid, glucose) sensors, thermal stimulators, and humidity energy harvesters.

24 ave been conducted to evaluate the impact of stimulator architecture and geometry on stimuli features

25 Implantable cardiac vagal nerve stimulators are a promising treatment for ventricular ar

26 The results demonstrate that these stimulators are able to deliver osteoconductive stimuli.

27 O generators, a number of sGC activators and stimulators are currently in clinical trials aiming to s

28 Clinically approved neural stimulators are limited by battery requirements, as well

29 Bioresorbable electronic stimulators are of rapidly growing interest as unusual t

30 When warm thermal stimulators are placed on the ring and index fingers of

31 e-scale integration of ultrathin sensors and stimulator arrays in multiple layers.

32 resolves the longstanding question of where stimulators bind and provides a path forward for drug di

33 These data indicated that stimulators bind to a conserved cleft between two subdom

34 Using NMR, we also examined stimulator binding to sGC from M. sexta and bacterial H-

35 The localization of stimulator binding to the sGC heme domain reported here

36 e bulkier tryptophan residues directly block stimulator binding.

37 B lymphocyte stimulator (BLyS) engenders survival and antibody secret

38 ion-inducing ligand (APRIL) and B-lymphocyte stimulator (BLyS), are important for the survival, proli

39 design and fabrication of a micro-scale cell stimulator capable of simultaneously providing mechanica

40 administered under general anesthesia, and a stimulator coil consisting of 2 individual cone-shaped c

41 d significantly enhanced responses to OVA(+) stimulators compared to sham-operated controls.

42 photolyzable diazirine derivative of a novel stimulator compound, IWP-051, and MS analysis, we locali

43 e sGC show clinical promise, but where these stimulator compounds bind and how they function remains

44 n's disease (PD) implanted with a deep brain stimulator (DBS) to test the hypothesis that the beta wa

45 ty effort of sharing and developing a common stimulator design for vision research.

46 li distributions were observed for different stimulator designs and different external excitations.

47 cremoris and Lc. lactis subsp. lactis showed stimulator effects (160%).

48 myelinated cochlear nerve fiber coupled to a stimulator-electrode-tissue interface.

49 strate the capability of this general visual stimulator experimentally in the in vitro mouse retinal

50 ith acute HCV infection; inducible T-cell co-stimulator expression correlates with production of HCV-

51 sponse to parasite stimulation, as a rosette-stimulator for Plasmodium falciparum- and P. vivax-IRBC.

52 CPEC appears to be a potent stimulator for switching the anti-angiogenic SMC phenoty

53 ation as well as a Peltier-based temperature stimulator for thermogenetics.

54 diverse reverse transcriptases can be strong stimulators for slippage at slippage-prone template moti

55 The 3' part of the stimulator functions largely independently and acts at l

56 The co-stimulators ICOS (inducible T cell co-stimulator) and CD

57 stimulatory receptors, with the inducible co-stimulator (ICOS) being most notable.

58 vity but also increased CD3 and inducible co-stimulator (ICOS) expression on T cells.

59 e exposed to Tfh-cell-promoting inducible co-stimulator (ICOS) ligand.

60 eficient ILC2s including inducible T cell co-stimulator (Icos).

61 rkinson's disease (N = 22) during deep brain stimulator implantation surgery (14 females, 18 males).

62 nable stable, long-lived operation as distal stimulators in a rat model of peripheral nerve injuries,

63 ysLTs and their relationship with other ILC2 stimulators in the activation of human ILC2s.

64 guat, a novel oral soluble guanylate cyclase stimulator, in patients with heart failure and reduced e

65 Effective evaluation of human BAT stimulators is constrained by the current standard metho

66 NF family (BAFF), also known as B lymphocyte stimulator, is a ligand required for the generation and

67 KAP protein, MDI that recruits a translation stimulator, La-related protein (Larp), to the mitochondr

68 of intracellular ICOSL (inducible T-cell co-stimulator ligand, also known as ICOSLG) to the B-cell s

69 iogenesis-targeting moieties with angiogenic stimulator-loaded NPs could be incorporated into effecti

70 The miniaturized neural stimulator may facilitate closed-loop neurostimulation f

71 Inducible co-stimulator molecule (ICOS) and HLA-DR were used to defin

72 ensive mutational analysis of the frameshift stimulators (mRNA signals and 2A protein) analysing acti

73 CD40 is an important stimulator of autophagy and autophagic killing of Toxopl

74 ignificantly higher levels of IL-5, a potent stimulator of B-1 cell Ab production.

75 oxy-9Z-octadecenoic acid (12,13-diHOME) is a stimulator of BAT activity, and that its levels are nega

76 Cold is a potent stimulator of BAT, activating BAT primarily through the

77 suggest that the RSPO family is an important stimulator of beta-catenin activity in many human tumors

78 d HDAC5, whereas PTH stimulation of RANKL, a stimulator of bone resorption, requires CRTC2.

79 Surprisingly, JWU-A021 is also a potent stimulator of Ca(2+) influx through TRPA1 cation channel

80 sab (cfos) as a potent miR-101a target gene, stimulator of CM proliferation, and inhibitor of scar ti

81 From these studies, we identify RAD18 as a stimulator of CRISPR-mediated HDR.

82 ogue of C-type natriuretic peptide, a potent stimulator of endochondral ossification.

83 The IAA/DNP combination is a powerful stimulator of exosome secretion, and these stimulatory e

84 entifies JWU-A021 to be an especially potent stimulator of glucagon-like peptide-1 (GLP-1) secretion

85 As the most potent stimulator of GnRH/LH release, kisspeptin is believed to

86 g cyclic GMP-AMP (cGAMP) synthase (cGAS) and stimulator of IFN gene (STING) in human pDCs.

87 mammalian cells, cytosolic CDNs bind STING (stimulator of IFN gene), resulting in the production of

88 nd leads to activation of the cGAMP synthase-stimulator of IFN genes (cGAS-STING) pathway, independen

89 The cyclic GMP-AMP synthase/stimulator of IFN genes (cGAS/STING) pathway detects cyt

90 nced tumors but can be up-regulated by local stimulator of IFN genes (STING) activation.

91 We have also demonstrated that codelivery of stimulator of IFN genes (STING) agonists stimulates immu

92 sor, cyclic GMP-AMP synthase (cGAS), and the stimulator of IFN genes (STING) are required for pathoge

93 With the stimulator of IFN genes (STING) C terminus being extensi

94 deficiencies in IFN-alpha/beta signaling or stimulator of IFN genes (STING) exhibit exacerbated neur

95 STimulator of IFN Genes (STING) has been identified as a

96 discovered that the innate immune regulator stimulator of IFN genes (STING) is completely silenced i

97 lammasome, on the functional output from the stimulator of IFN genes (STING) pathway is poorly unders

98 ed by the cyclic GMP-AMP synthase (cGAS) and stimulator of IFN genes (STING) pathway to induce type I

99 As such, stimulator of IFN genes (STING), an adaptor molecule inv

100 d autophagy via the cytoplasmic DNA receptor stimulator of IFN genes (STING), as well as fusion of ph

101 ger cGAMP, which in turn binds and activates stimulator of IFN genes (STING), leading to induction of

102 ng pathways triggered by B. abortus involves stimulator of IFN genes (STING), which leads to producti

103 rucella abortus DNA involves TLR9, AIM2, and stimulator of IFN genes (STING).

104 These secondary messengers bind directly to stimulator of IFN genes (STING).

105 synthase and the downstream adaptor protein stimulator of IFN genes (STING).

106 2, and Mincle), and the cytosolic DNA sensor stimulator of IFN genes (STING).

107 vation of the downstream signaling effectors stimulator of IFN genes and NF-kappaB, but not TANK-bind

108 dency on IFI16, cyclic GMP-AMP synthase, and stimulator of IFN genes for type I IFN induction by a pa

109 analyses have revealed a major role for the stimulator of IFN genes pathway (STING pathway), which s

110 The stimulator of IFN genes pathway was discovered to be a p

111 oposed to act in the cyclic GMP-AMP synthase-stimulator of IFN genes pathway.

112 al-signaling protein (MAVS) and mice lacking stimulator of IFN genes protein (STING), 2 downstream se

113 pendent on cytosolic DNA sensing mediated by stimulator of IFN genes signaling.

114 The adaptor proteins STING (stimulator of IFN genes), MAVS (mitochondrial antiviral

115 and colleagues report on the role of STING (stimulator of IFN genes, TMEM173) in regulating critical

116 intracellular DNA triggers activation of the stimulator of IFN genes-dependent IFN-stimulatory DNA (I

117 , ADAM17, and the antiviral adaptor protein, stimulator of IFN genes.

118 an enhancer of GSIS in vivo and as a direct stimulator of insulin-independent glucose uptake is not

119 The stimulator of interferon (IFN) genes (STING) is a broad

120 Activation of the cyclic dinucleotide sensor stimulator of interferon (IFN) genes (STING) is critical

121 g the cyclic GMP-AMP synthase (cGAS) and the stimulator of interferon (IFN) genes (STING), two crucia

122 3'-cGAMP can bind the adaptor protein STING (stimulator of interferon [IFN] genes) to activate the pr

123 on and activation of cyclic GMP-AMP synthase-stimulator of interferon genes (cGAS-STING) in APCs, res

124 mage response (DDR), cyclic GMP-AMP synthase-stimulator of interferon genes (cGAS-STING) pathway acti

125 tudy, we studied the cyclic GMP-AMP synthase-stimulator of interferon genes (cGAS-STING) pathway by u

126 of interferon-mediated antiviral responses - stimulator of interferon genes (STING) - has now emerged

127 -I) response by sequestering and attenuating stimulator of interferon genes (STING) activation.

128 dermines host antiviral responses, including stimulator of interferon genes (STING) activation.

129 Stimulator of interferon genes (STING) acts as a cytopla

130 he innate immune response that activates the stimulator of interferon genes (STING) adaptor and induc

131 the production of type I interferons via the stimulator of interferon genes (STING) adaptor.

132 Furthermore, by loading a stimulator of interferon genes (STING) agonist, hNVs lea

133 gers both the cyclic GMP-AMP synthase (cGAS)-stimulator of interferon genes (STING) and Toll-like rec

134 Cyclic dinucleotide (CDN) agonists of stimulator of interferon genes (STING) are a promising c

135 Activation of the STimulator of INterferon Genes (STING) by DMXAA (5,6-dim

136 chromatin fragments and then activating the stimulator of interferon genes (STING) cytosolic DNA-sen

137 ctive puncta that promote lysosomal-mediated stimulator of interferon genes (STING) degradation.

138 apamycin (mTOR) to prevent the activation of stimulator of interferon genes (STING) expression and im

139 The host protein Stimulator of Interferon Genes (STING) has been shown to

140 Stimulator of interferon genes (STING) has been shown to

141 Stimulator of interferon genes (STING) is a key cytosoli

142 Stimulator of interferon genes (STING) is a receptor in

143 Stimulator of interferon genes (STING) is an endoplasmic

144 Stimulator of interferon genes (STING) is essential for

145 Stimulator of interferon genes (STING) is known be invol

146 dominant gain-of-function mutations in human stimulator of interferon genes (STING) lead to a severe

147 Stimulator of interferon genes (STING) links innate immu

148 e modulators consisting of an agonist of the stimulator of interferon genes (STING) pathway and an ag

149 Activation of the stimulator of interferon genes (STING) pathway can enhan

150 Since its discovery 12 years ago, the stimulator of interferon genes (STING) pathway has attra

151 evidence indicates the critical role of the stimulator of interferon genes (STING) pathway in antitu

152 ed interferon signaling mediated by the cGAS-stimulator of interferon genes (STING) pathway in patien

153 The Stimulator of Interferon Genes (STING) pathway initiates

154 The stimulator of interferon genes (STING) pathway plays an

155 activate the cyclic GMP-AMP synthase (cGAS)-stimulator of interferon genes (STING) pathway to induce

156 ctivating the cyclic GMP-AMP synthase (cGAS)-stimulator of interferon genes (STING) pathway(3).

157 enting cell maturation via the intracellular stimulator of interferon genes (STING) pathway, rather t

158 engers in the cyclic GMP-AMP synthase (cGAS)-stimulator of interferon genes (STING) pathway, which pl

159 econd messenger that activates the antiviral stimulator of interferon genes (STING) pathway.

160 sponse to cytosolic dsDNA that activates the stimulator of interferon genes (STING) pathway.

161 vation of the cyclic GMP-AMP synthase (cGAS)-stimulator of interferon genes (STING) pathway.

162 ctively hyperresponsive to activators of the stimulator of interferon genes (STING) protein-a key reg

163 A and produces cGAMP, which in turn binds to stimulator of interferon genes (STING) to activate IFN-I

164 Cytosolic DNA engages stimulator of interferon genes (STING) to activate TANK-

165 messenger that activates the adaptor protein stimulator of interferon genes (STING) to induce type I

166 a is a vita-PAMP, engaging the innate sensor stimulator of interferon genes (STING) to mediate endopl

167 transmembrane protein 173 (TMEM173) encoding stimulator of interferon genes (STING) underlie a recent

168 Stimulator of interferon genes (STING) was initially des

169 second messenger that binds to and activates stimulator of interferon genes (STING)(3-9).

170 P and prevent the activation of the receptor stimulator of interferon genes (STING)(5-7).

171 Here, we report that a natural agonist of stimulator of interferon genes (STING), 2'3'- cyclic gua

172 GMP-AMP (cGAMP), which binds to the adaptor STIMULATOR OF INTERFERON GENES (STING), activating an IN

173 response by oxidizing Cysteine 147 on murine stimulator of interferon genes (STING), an ER-associated

174 ways, such as cyclic GMP-AMP synthase (cGAS)-stimulator of interferon genes (STING), and propagation

175 cGAS) and its downstream signalling effector stimulator of interferon genes (STING), as well as the m

176 This effect is dependent on stimulator of interferon genes (STING), but not the Toll

177 pon activation, which binds to and activates stimulator of interferon genes (STING), leading to IFN p

178 endent upon the DNA-sensing pathway adaptor, stimulator of interferon genes (STING), through the reco

179 ome-like signaling events, driven in part by stimulator of interferon genes (STING), to unexpectedly

180 cGAMP activates stimulator of interferon genes (STING), which activates

181 o responders to anti-CD47 immunotherapy in a stimulator of interferon genes (STING)- and interferon-d

182 Patients with stimulator of interferon genes (STING)-associated vascul

183 gh mitosis or loss of pattern recognition by stimulator of interferon genes (STING)-cGAS impaired int

184 , as well as induction of AIM2-dependent and stimulator of interferon genes (STING)-dependent autopha

185 d to down-regulate the NF-kappaB pathway and stimulator of interferon genes (STING)-dependent cytokin

186 exhibit antitumor immunity that occurs in a stimulator of interferon genes (STING)-dependent manner

187 vation of cyclic GMP-AMP synthase (cGAS) and stimulator of interferon genes (STING).

188 c GMP-AMP (cGAMP), which binds and activates stimulator of interferon genes (STING).

189 g or the endoplasmic reticulum (ER) adapter, stimulator of interferon genes (STING).

190 cleotide cGAMP, followed by the induction of stimulator of interferon genes (STING).

191 Stimulator of interferon genes (STING, also known as MIT

192 Given the integral role of stimulator of interferon genes (STING, TMEM173) in the i

193 GMP-AMP (cGAMP) that binds to and activates stimulator of interferon genes (STING; also known as TME

194 For example, a gain-of-function mutation in stimulator of interferon genes (STING; N153S) upregulate

195 rt on a cyclic GMP-AMP adjuvant, the natural stimulator of interferon genes agonist, providing eviden

196 olymer, PSC7A, can achieve activation of the stimulator of interferon genes and antigen delivery upon

197 n of DNA sensors cyclic GMP-AMP synthase and stimulator of interferon genes in wild-type (WT) mice.

198 diguanylate monophosphate, an agonist of the stimulator of interferon genes pathway, and monophosphor

199 or inhibitors of the cyclic GMP-AMP synthase/stimulator of interferon genes pathway, which recruited

200 protein 16 (IFI16) detect DNA and signal via stimulator of interferon genes protein (STING).

201 Mase2, and pro-aging/pro-inflammatory STING (Stimulator of interferon genes) gene expression without

202 STING (stimulator of interferon genes) is an important innate i

203 STING (STimulator of INterferon Genes) mediates protective cell

204 -cGAMP), the natural agonist of STING (i.e., stimulator of interferon genes) or after infection with

205 vate the cGAS-STING (cyclic GMP-AMP synthase-stimulator of interferon genes) pathway and engage the a

206 y, the CGAS (cyclic GMP-AMP synthase)-STING (stimulator of interferon genes) pathway mitigates activa

207 GAS-STING (cyclic GMP-AMP synthase linked to stimulator of interferon genes) pathway, leading both to

208 of the cytosolic DNA sensing adaptor STING (stimulator of interferon genes) play a critical role in

209 Pharmacological activation of the STING (stimulator of interferon genes)-controlled innate immune

210 gonist of the interferon gene inducer STING (stimulator of interferon genes).

211 ntiviral response via the DNA sensor, STING (stimulator of interferon genes).

212 TRIM29 induces K48-linked ubiquitination of Stimulator of interferon genes, a key adaptor in double-

213 a focus on complement, the adapter molecule Stimulator of Interferon Genes, natural killer cells, my

214 ng, as exemplified by the recently described stimulator of interferon genes-associated vasculopathy w

215 ic activation of the cyclic GMP-AMP synthase-stimulator of interferon genes-TANK-binding kinase-inter

216 vasoactive intestinal polypeptide, a potent stimulator of ion secretion classically produced by ente

217 is secreted by white cells only, is a potent stimulator of macrophage chemokinesis, whose activity is

218 Chlamydial LOS was also a poor stimulator of maturation of bone marrow-derived dendriti

219 cute exercise and identified VEGF-A as a key stimulator of Mdm2 phosphorylation on Ser(166) (p-Ser166

220 The photosensitizer is also a potent stimulator of P-glycoprotein (P-gp).

221 ere mimics the activity of a structured mRNA stimulator of PRF.

222 e signals; kisspeptin has emerged as a major stimulator of puberty, and makorin RING finger protein 3

223 embolic pulmonary hypertension, riociguat, a stimulator of soluble guanylate cyclase, has proven effi

224 e show that MCB-613, a potent small molecule stimulator of steroid receptor coactivators (SRCs) atten

225 lterations associated with activation of the stimulator of the cyclic GMP-AMP synthase interferon gen

226 ociated DYRK1A kinase has been reported as a stimulator of the developmentally important Hedgehog (Hh

227 envelope of most bacteria, and also a potent stimulator of the eukaryotic immune system.

228 otent epithelial proliferation and migration stimulator of the oral mucosa as a potential therapy to

229 e that binds to chromosomal DNA; ParB is the stimulator of the ParA ATPase and specifically binds to

230 s, suggests that IL-33 might be an important stimulator of tissue-localized loss of normal Treg cell

231 Despite acting as a direct stimulator of transcription, histone butyrylation compet

232 The aim was to determine whether leucine, a stimulator of translation initiation and skeletal muscle

233 nstrate that Chi3l1 is a multifaceted immune stimulator of tumor progression and metastasis whose ela

234 Despite the classical role of IRF-7 as a stimulator of type I interferon (IFN) transcription, the

235 ically, downregulated expression of IL-33, a stimulator of type II innate lymphoid cells, in lung epi

236 However, their effect as direct stimulators of B lymphocytes has not been yet fully eluc

237 thylase TET1 is suppressed by cold and other stimulators of beige adipocyte thermogenesis.

238 Dietary lipids are one of the most effective stimulators of carotenoid absorption, but very limited d

239 tro, DLL4-deficient APCs were less efficient stimulators of CD4(+) T cell activation, metabolism, pro

240 We hypothesized that, as stimulators of early origin activation, Fkh1 and Fkh2 ab

241 cysteine were examined as inhibitors and/or stimulators of fresh-cut potato browning.

242 oter activity of human KISS1 and TAC3, 2 key stimulators of GnRH secretion.

243 in an antigen-dependent manner became potent stimulators of localized antigen-specific inflammatory r

244 This identifies THs as potent endocrine stimulators of mitochondrial function in human epidermis

245 Isoforms 01 and 03 were the most potent stimulators of patients' T cells.

246 uvate (PEP), Pro, and Ala as the most potent stimulators of plant leaf R(N) Using metabolite combinat

247 Stimulators of soluble guanylate cyclase (sGC) enhance N

248 es with inhibitors of phosphodiesterase 5 or stimulators of soluble guanylyl cyclase rapidly enhanced

249 isolated from C3H/HeJ mice were less potent stimulators of T lymphocyte proliferation and TH1/TH17 p

250 Aha-type co-chaperones are the most potent stimulators of the Hsp90 ATPase activity but the relatio

251 (TLR-9) in endosomes and are well described stimulators of the innate and adaptive immune system.

252 tigens at their cell surface that are potent stimulators of the innate immune response, and yet the c

253 Stimulator-of-interferon genes (STING) is vital for sens

254 lial cells through the inhibition of RB1 and stimulator-of-interferon-genes (STING) to propagate cell

255 ngers of one hand, and a neutral-temperature stimulator on the middle finger, all three fingers feel

256 derwent an attempted sphenopalatine ganglion stimulator or sham stimulator placement procedure were i

257 ide the TMS coil, starting at 25% of maximum stimulator output (MSO) and increasing in steps of 2% un

258 cy MST (i.e., 25 Hz MST) (N = 36) using 100% stimulator output.

259 atment of rats with the first-in-class NAMPT stimulator, P7C3-A20, prevented behavioral and histologi

260 engerRNAs, proteins, metabolites and various stimulators participating in regulatory networks.

261 aluated, including soluble guanylate cyclase stimulators, phosphodiesterase type 5 inhibitors, sodium

262 laparoscopy and connected to a dual-channel stimulator placed subcutaneously.

263 d sphenopalatine ganglion stimulator or sham stimulator placement procedure were included in the safe

264 ntagonist SCH 23390, but the infusion of PKC stimulator PMA does not.

265 lying the antiinflammatory effect of the sGC stimulator praliciguat (PRL) in the liver.

266 ts with HFpEF, the soluble guanylate cyclase stimulator praliciguat, compared with placebo, did not s

267 rase-5 inhibitors, soluble guanylate cyclase stimulators, prostacyclin analogues, and prostacyclin re

268 We demonstrate that wireless ME stimulators provide therapeutic deep brain stimulation i

269 Autophagy stimulator rapamycin reversed sesamol-induced apoptosis

270 Expression levels of B lymphocyte stimulator receptor 3 and programmed cell death 1 on B c

271 and vericiguat, a soluble guanylate cyclase stimulator, reduces heart failure hospitalization in hig

272 polysaccharide (LPS) is a toxic inflammatory stimulator released from the outer cell membrane of Gram

273 rst-in-class soluble guanylate cyclase (sGC) stimulator riociguat was recently introduced as a novel

274 were receiving the soluble guanylate cyclase stimulator riociguat.

275 rally involve single ribosomes responding to stimulator sequences in their engaged mRNAs.

276 Small GTP-binding protein GDP-dissociation stimulator (SmgGDS) proteins are chaperones that bind an

277 However, few stimulator solutions simultaneously offer high spatio-te

278 dditionally, the hippocampal infusion of PKA stimulator Sp-cAMP reverts the effect of D1/D5 dopaminer

279 ey T helper 17 (T(H)17) cell differentiation stimulator, STAT3(3,4), is subject to reversible S-palmi

280 an anti-parasite response via the interferon stimulator STING.

281 clathrin-coated pits and that physiological stimulators such as GPCR ligands induce ADAM17-mediated

282 the middle digit was lifted off the thermal stimulator, suggesting that tactile stimulation is neces

283 ion of TCR/CD3 genes, T cell co-receptors/co-stimulators, T cell activation and signal-transduction g

284 Furthermore, typical therapeutic stimulators target large nerve bundles that innervate mu

285 leadless and battery-free implantable neural stimulator that is 1.7 mm(3) and that incorporates a pie

286 e approaches have yet to produce a miniature stimulator that operates at clinically relevant high fre

287 Here, we employed a mechanical stimulator that reliably positioned animals' hands in di

288 nables miniature magnetically powered neural stimulators that operate up to clinically relevant frequ

289 hether stimulation occurs are encoded by the stimulator through backscatter modulation and are demodu

290 Here we show NLRP3 inflammasome stimulators trigger Src homology-2 domain containing pro

291 resulting in the discovery of once daily sGC stimulator vericiguat (compound 24, BAY 1021189), curren

292 Reduced Ejection Fraction) trial on the sGC stimulator vericiguat in HFrEF, the main open questions

293 uate the Efficacy and Safety of the Oral sGC Stimulator Vericiguat to Improve Physical Functioning in

294 ty of a novel oral soluble guanylate cyclase stimulator, vericiguat, on quality of life and exercise

295 Covalent attachments to the stimulator were also identified in bacterial homologs of

296 on sensors, pressure sensors, and electrical stimulators, which are made via spray printing of silver

297 Praliciguat, an oral sGC stimulator with extensive distribution to the liver, was

298 a hand-held external transceiver provide the stimulator with power and bidirectional communication.

299 Here, we present a flexible, spatial visual stimulator with up to six arbitrary spectrum chromatic c

300 NO and the sGC-specific stimulator YC-1 induce a 71 degrees rotation of the heme