ライフサイエンスコーパス: stimulation of @2 by

1 The most conspicuous anomaly was a large stimulation of IS by 1 mmol/L glucose.

2 Finally, stimulation of Lyn expression by 1,25-dihydroxyvitamin D

3 receptor homolog FOLR-1 is required for the stimulation of germ cells by 10-formyl-tetrahydrofolate-

4 in the adenoma cell line, RG/C2, resulted in stimulation of growth by 10 micromol/L PGE(2) and promot

5 ces (TM), alphaTM2 and alphaTM4, abolish the stimulation of activity by 18:0/20:4 PC but do not affec

6 explore the molecular basis for the observed stimulation of catalytic activity by 2-methylimidazole i

7 e observed that, in SOD1-G93A microglia, the stimulation of P2X7 receptor by 2'-3'-O-(benzoyl-benzoyl

8 p2 and STAT-3 mediate, at least in part, the stimulation of Hsp70 expression by 4PBA.

9 and therefore suggest that motion-modulated stimulation of canal afferents by a vestibular prosthesi

10 henotypes were attenuated by pharmacological stimulation of PDH or by a ketogenic diet, two treatment

11 roblasts blocks caveolar endocytosis and the stimulation of signaling by a GSL with natural stereoche

12 Previous studies have shown that electrical stimulation of the cochlea by a cochlear implant promote

13 The approach is based on specific stimulation of ATP hydrolysis by ABCG2 transporters with

14 In contrast, stimulation of alpha7 nAChRs by acetylcholine may mediat

15 Stimulation of lymphatic endothelium by acetylcholine or

16 ticotrophin-releasing hormone (CRH) and then stimulation of the adrenal by ACTH.

17 s from enhanced osteoblastic support and the stimulation of VEGF by ACTH; the latter is largely respo

18 Intense stimulation of sensory neurons by action potentials or T

19 amino acids is a prerequisite for subsequent stimulation of mTORC1 by activating amino acids.

20 Additionally, stimulation of IL1beta secretion by activation of c-Met

21 ocampus and neocortex, reflecting widespread stimulation of mTOR signaling by acute seizure activity.

22 Stimulation of peripheral chemoreceptors by acute hypoxi

23 e progression, it is possible that continued stimulation of NK cells by ADCC during chronic HIV infec

24 X-irradiation of the host liver and mitotic stimulation of the hepatocytes by adenovector-based expr

25 gnaling pathway is governed by both hormonal stimulation of cAMP generation by adenylyl cyclases (act

26 Stimulation of death receptors by agonists such as FasL

27 These data afford a mechanism for rapid stimulation of dendritic growth by all-trans-retinoic ac

28 Stimulation of mast cells by allergens induces two mamma

29 In airway epithelial cells (AECs), stimulation of PAR2 by allergens and proteases triggers

30 In vivo stimulation of iNKT cells by alpha-galactosyl-ceramide w

31 ly infected cells could be reactivated after stimulation of the TCR by alpha-CD3/CD28 antibodies.

32 osine diphosphate-bound Rag mutant prevented stimulation of mTORC1 by amino acids.

33 Consistent with FDPS inhibition, stimulation of Vgamma2Vdelta2 cells by aminobisphosphona

34 trisphosphate in single cells, we found that stimulation of CaR by an increase in the extracellular C

35 of bile acids caused analgesia to mechanical stimulation of the paw by an opioid-dependent mechanism.

36 The findings suggest that stimulation of neutrophils by ANCA causes release of fac

37 The stimulation of NHE3 by ANG II was dependent on changes i

38 Additionally, stimulation of aldosterone secretion by AngII, but not b

39 at forebrain structures are key sites in the stimulation of drinking behavior by AngII.

40 Stimulation of ERK5 by angiotensin II is blocked upon ph

41 r apoE3 (60% vs. 30%) due to more pronounced stimulation of APP recycling by apoE4 than apoE3.

42 Atrial natriuretic peptide also prevented stimulation of calpain activity by ATP, taurolithocholat

43 ngle mutations to these residues abolish the stimulation of dephosphorylation by ATP.

44 Here, we demonstrate that stimulation of EGFR activation by ATP in airway epitheli

45 Stimulation of Rankl mRNA by ATRA was competitively inhi

46 selective inhibitor, PKI-166, prevented the stimulation of NF-kappaB by axonal membranes.

47 rmal fibroblasts, and Egr-1 was required for stimulation of collagen by Bcr-Abl.

48 Models for the allosteric stimulation of Int activity by beta5 strand contacts are

49 The stimulation of mesodermal precursors by bFGF and activin

50 Stimulation of ENaC activity by bile acids is accompanie

51 a novel and quick protocol for studying the stimulation of anaerobic bioprocesses by bioavailable es

52 RAD51 nucleoprotein filament conformation in stimulation of DNA pairing by BLM.

53 reover, knockdown of CD81 did not affect the stimulation of hepcidin expression by BMP6 but increased

54 In vitro stimulation of endothelial cells by BMP9 and BMP10 incre

55 The stimulation of eNOS activity by BMPRII ligands was large

56 Therefore, stimulation of the parathyroid by both hypocalcemia and

57 Significantly, we find that stimulation of ATR by BPDE-damaged DNA exhibits strong d

58 Stimulation of NO production by bradykinin or carbachol

59 Similar to the in vitro reaction, the stimulation of Rpb1 ubiquitination by BRCA1 in cells occ

60 The stimulation of accessibility induced by Ca(2+) at the S2

61 outer surface of the plasma membrane and the stimulation of its secretion by Ca(2+) and protein kinas

62 The in vitro results indicate that stimulation of the CaSR, by Ca(2+) or by the calcimimeti

63 e is a metabolic target of caffeine and that stimulation of Cox activity by caffeine via blockade of

64 Moreover, stimulation of NRG1 cleavage by calcyon was recapitulate

65 Our data thus support the contention that stimulation of oral receptors by caloric foods may not b

66 ng phosphodiesterase activity and subsequent stimulation of CFTR by cAMP-dependent protein kinase A.

67 erm demonstrate a major role for Epac in the stimulation of exocytosis by cAMP.

68 mall GTPase methylation occurs seconds after stimulation of starving cells by cAMP and returns quickl

69 Stimulation of transcription by cAMP was potentiated by

70 Stimulation of TRPV1 by capsaicin down-regulates VACCs b

71 that controls EDG-1 up-regulation following stimulation of T cells by CCR7/CCL19.

72 s of prostate cancer displays an exaggerated stimulation of transcriptional activity by CDK6.

73 phosphate sink" possibly to off-set the over-stimulation of the kinase by certain types of chemorecep

74 Stimulation of TNF by cFb was dependent on TLR-4 and MyD

75 ory' attributes the central chemoreflex (the stimulation of breathing by CNS acidification) to the cu

76 Baseline motor behavior is not affected, but stimulation of locomotor activity by cocaine is impaired

77 The observed stimulation of primer synthesis by cognate DnaB(BA) is t

78 absence of MHC II expression by DCs, direct stimulation of Tregs by cognate Ag/MHC II complexes enha

79 Moreover, cooperative stimulation of hepatocyte proliferation by combined TNF

80 melanosome transport along microtubules, and stimulation of ERK by constitutively active MEK1/2 stimu

81 n which axonal sorting is accomplished by OR stimulation of cAMP production by coupling to Galphas.

82 Finally, CerS dimers are formed upon rapid stimulation of ceramide synthesis by curcumin.

83 ncell autonomous defect, caused by exuberant stimulation of osteoclastogenesis by Cx43-deficient bone

84 ts flanking amino acids is critical for cGMP stimulation of Ser102 phosphorylation by cyclic nucleoti

85 iation but through a mechanism targeting the stimulation of transcription elongation by cyclin-depend

86 Stimulation of endothelial cells by cysLTs induced mRNA

87 tokines: aminoguanidine does not inhibit the stimulation of hepcidin transcription by cytokines.

88 ic oxide does not seem to be involved in the stimulation of hepcidin transcription by cytokines: amin

89 ono-unsaturated fat diets prevent the normal stimulation of CETP activity by dietary cholesterol.

90 r the first time allows in vitro hemodynamic stimulation of cardiomyocytes by directly coupling cell

91 ment of a nucleotide for DNA binding and the stimulation of ATPase activity by DNA indicate that the

92 Importantly, stimulation of binding by Doc1 also requires that the su

93 rotarod motor tests; cyclic AMP responses to stimulation of D1 receptors by dopamine was selectively

94 hese results suggest an alternative mode for stimulation of Atm by DSBs in which Atm autophosphorylat

95 We found that stimulation of Kiss1 expression by E(2) in the AVPV and

96 61 may be mediated by activation of CREB, 2) stimulation of neurogenesis by EGb 761 may contribute to

97 Our data indicate that stimulation of GTP hydrolysis by eIF5B requires the comp

98 Hormonal stimulation of ENaC activity by either forskolin or aldo

99 of ER-alpha in the absence of estrogen, and stimulation of ER-alpha by either Ca(2+) and/or estrogen

100 Stimulation of whole blood by either BCG or BCG plus IFN

101 In addition, the stimulation of neurogenic spots by electrical, mechanica

102 Stimulation of forest productivity by elevated concentra

103 Stimulation of mycorrhizal production by elevated CO2 wa

104 que open-air field facility to show that the stimulation of soybean yield by elevated [CO2] diminishe

105 ent nitrogen (N) availability constrains the stimulation of terrestrial productivity by elevated CO2

106 Interestingly, the stimulation of angiogenesis by EMD was significant only

107 ere we focus on mechanisms that underlie the stimulation of G by ephrins.

108 The VSE is also required for Vta1-dependent stimulation of Vps4 by ESCRT-III subunits.

109 Stimulation of anaerobic digestion by essential trace me

110 Stimulation of transcription by extracellular signals is

111 Stimulation of cAMP formation by forskolin also activate

112 a ligand or C/EBPalpha are not necessary for stimulation of adipogenesis by FOXC2-Eng, at least low l

113 Stimulation of GCs by FSH leads to their proliferation a

114 Here, we show that stimulation of signaling by function-triggering L1 antib

115 Stimulation of renin by furosemide was not affected by m

116 We also provide evidence that stimulation of interleukin-6 by galectin-3-binding prote

117 ding to activated Galpha(13) and ablates the stimulation of p115 by Galpha(13).

118 the helical domain of Galpha(13) also affect stimulation of p115 by Galpha(13).

119 ent substrates of gamma-secretase and direct stimulation of processing by gamma-secretase.

120 ectile dysfunction, ameliorates high glucose stimulation of matrix proteins by generating H2S in podo

121 Alpha2-adrenergic agonists also reduced stimulation of ERK1/2 by glucagon-like peptide 1 and KCl

122 y, we show that induction of EMT by TGF-beta stimulation of human keratinocytes, by glycogen synthase

123 Stimulation of Bcy1 phosphorylation by Gpb1 and Gpb2 pro

124 nduced by the inhibition of Ca(2+) influx or stimulation of Na(+) influx by gramicidin was accompanie

125 In this study, we find that stimulation of PC6 cells by growth factors, including ne

126 duced glutathione in agreement with a 3-fold stimulation of ATPase activity by GSSG.

127 n compared with mononucleosomes and that the stimulation of H3 methylation by H1 requires dinucleosom

128 ure or epithelial stem cell maintenance, and stimulation of anagen by hair plucking caused follicular

129 external Ca2+ acts before rather than after stimulation of SACY by HCO3(-).

130 Rapid initial stimulation of lamellipodia formation by HDL via SR-BI,

131 Stimulation of DNA resection by hExo1 is independent of

132 In addition, ERK mediated the stimulation of mTOR by HFS.

133 Stimulation of the alpha1aAR by high dose phenylephrine

134 ng the furin cleavage site did not alter the stimulation of hepcidin expression by Hjv in mice.

135 or in the required conformational change for stimulation of flavin reduction by HPA.

136 nal perturbations and also abolished WT-like stimulation of ATP hydrolysis by HscA.

137 To elucidate the structural basis for ATPase stimulation of human Hsp90 by human Aha1, we have develo

138 in brain PCO(2) or pH and contribute to the stimulation of breathing elicited by hypercapnia or meta

139 The underlying mechanism of the noticed stimulation of SGK1 expression by hypoxia includes de-re

140 B and T cells plays an important role in the stimulation of Ab responses by IFN-alphabeta.

141 The stimulation of MSCs by IFN-gamma and TNF-alpha released

142 Rather, stimulation of AKT by IGF-I was significantly higher and

143 Stimulation of AKT by IGF-I, mimicked also by a constitu

144 The stimulation of autophagy by IL-6 is regulated via multip

145 n at the mucosal interface that explains how stimulation of epithelial cells by IL-4 and IL-13 contri

146 In contrast, the stimulation of movement by increased dopamine is much mo

147 Mechanical stimulation of the artery, by increased intraluminal pre

148 PF-04957325) potentiates adrenocorticotropin stimulation of steroidogenesis by increasing cAMP-depend

149 Stimulation of attachment by incubation of untransfected

150 retinal ganglion cells (RGCs), coupled with stimulation of RGCs by inflammation and cAMP, dramatical

151 Dexras1 seemed to inhibit PMA stimulation of AC2 by interfering with PKCdelta autophos

152 In contrast to Y126C-Y126C, trans-stimulation of methotrexate uptake by intracellular fola

153 Frequency-specific stimulation of that pathway by intraneural stimulation m

154 We found that nutrient stimulation of insulin secretion by isolated rat islets

155 intracellular calcium mobilization, and the stimulation of cAMP formation by isoproterenol were all

156 Stimulation of fatty uptake by isoproterenol required bo

157 The present study demonstrated that stimulation of CXCR4 by its ligand, CXCL12, induced tran

158 auses increased basal TF expression and that stimulation of EGFR by its ligand, EGF, leads to a marke

159 Stimulation of EGFR by its natural ligand, EGF, induced

160 y of ATGL broadens to the sn-1 position upon stimulation of the enzyme by its co-activator CGI-58.

161 e dissociation from BiP 6-fold and abolished stimulation of ATP hydrolysis by J-domain cofactor.

162 o autophosphorylate, whereas KaiB blocks the stimulation of KaiC by KaiA, which allows KaiC to autode

163 Stimulation of SK activity by killed M.tb, live Staphylo

164 These findings suggest that the potent stimulation of naive pluripotency by LIF/Stat3 is attrib

165 Further, maximal stimulation of Th1 cells by lipopolysaccharide (LPS) did

166 The stimulation of IRF-4 by LMP-1 requires signaling from LM

167 he center of the display; thus, differential stimulation of the fovea by local contrast changes could

168 Chronic stimulation of the beta2AR by long acting beta-agonists

169 at SL-deficient plants are more sensitive to stimulation of bud growth by low concentrations of local

170 Stimulation of keratinocyte proliferation by low Ca(2+)

171 of beta-adrenergic agonists to act following stimulation of cells by LPA as may occur during beta-adr

172 3K/AKT-dependent component; 2) reduced acute stimulation of NHE3 activity by LPA/LPA5R stimulation; a

173 Stimulation of macrophages by LPS, but not polarization

174 Robust stimulation of platelets by LPS therefore also required

175 specific role of the IFNAR-STAT2 axis in the stimulation of proinflammatory cytokines by LPS in cDCs.

176 Stimulation of mucin release by lubiprostone may be prot

177 e effect through cytokine regulation and the stimulation of additional opsonins by macrophages.

178 Stimulation of CCL2 by macrophages upon pneumococcal inf

179 The robust stimulation of dopamine transmission by MDPV predicts se

180 of autophagy in eosinophils, and additional stimulation of autophagy by means of pharmacologic inhib

181 Stimulation of PKG by measures such as sildenafil admini

182 Stimulation of dNKT hybridomas by microbial PG was indep

183 uired for symbiotic signal transduction upon stimulation of root cells by microbial signaling molecul

184 Stimulation of TLR by microbial constituents is known to

185 In this study, we show that stimulation of innate pathways by microbiota-derived lig

186 Stimulation of hepatocyte differentiation by miR-122 was

187 In contrast, the trans-stimulation of GSH efflux by MK571 increased the cleavag

188 s that while ATPase activity is required for stimulation of splicing by Mss116, helicase activity is

189 Chemical stimulation of cAMP production by Mtb within macrophages

190 del to examine monocyte/macrophage-dependent stimulation of fibroblasts by Mtb in the regulation of c

191 er, until now, the mechanism underlying this stimulation of transcription by mTERF was not understood

192 ked intracellular Ca(2+) rise in response to stimulation of mouse TRPC4beta by mu-opioid receptors.

193 The stimulation of fusion by Munc18c is specific to its cogn

194 at initiate and accompany, respectively, the stimulation of fluid secretion by muscarinic ligands.

195 This is consistent with metformin stimulation of glucose uptake by muscle and inhibition o

196 xpression of hnRNPK with N-WASP reverses the stimulation of cell spreading by N-WASP, and this effect

197 ith subtoxic doses of curcumin combined with stimulation of ATP hydrolysis by Na(+),K(+)-ATPase with

198 difference in either cosubstrate binding or stimulation of melibiose transport by Na(+) or Li(+), bu

199 Stimulation of ATP7B trafficking by nanobodies in the ab

200 Stimulation of astrocytes by neuronal activity and the s

201 f the dominant negative Ras and Raf, reduced stimulation of ERK1/2 by NNK.

202 ting that P2X7 receptors are not involved in stimulation of ATP release by NPPB.

203 -intron from spliceosomes, are refractory to stimulation of RNA unwinding by Ntr1.

204 of the E2P ground state, thus explaining the stimulation of dephosphorylation by nucleotide-induced t

205 amus (PMv), which has been implicated in the stimulation of gonadotropin release by olfactory cues, c

206 In cell culture, stimulation of glioma cells by overexpressing Ang2 or ex

207 s binding site on PH strongly attenuates the stimulation of RhoA observed by overexpression of five o

208 The pRb requirement of the stimulation of Cbfa1 activity by p204 was established in

209 The stimulation of tumor growth by p62 accumulation in FIP20

210 ting versus drug abuse refers to the sensory stimulation of oral receptors by palatable foods, a feat

211 regation in vivo, proving that intracellular stimulation of ATP hydrolysis by ParG is a key regulator

212 The stimulation of TLRs by pathogen-derived molecules leads

213 Thus, stimulation of neoplastic growth by Pax5 occurs through

214 Adrenergic stimulation of H9c2 cardiomyocytes by phenylephrine (PE)

215 Stimulation of IP3 production by phenylephrine or endoth

216 Stimulation of pagC expression by PhoP requires SlyA.

217 After stimulation of MM6 cells by phorbol myristate acetate an

218 istics of the full-length protein, including stimulation of DNA binding by physical interaction with

219 However, the stimulation of signaling by PI3K/PKB also can activate s

220 The results show that stimulation of PPARgamma by pioglitazone did not affect

221 presence of WNK4 allows amplification of the stimulation of channel by PKC.

222 Stimulation of macropinocytosis by platelet-derived grow

223 The stimulation of DNA synthesis by Poleta with PCNA or Ub-P

224 aspase 3, caspase 6, and caspase 8 after the stimulation of LPS, followed by poly(ADP-ribose) polymer

225 through mechanisms distinct from the direct stimulation of CK2 by polyamines in vitro as previously

226 mpatibility complex (MHC-II) proteins govern stimulation of adaptive immunity by presenting antigenic

227 Our finding of non-enzymatic stimulation of matriptase activation by prostasin and ac

228 We have now determined that this stimulation of VEGF by RA is mediated through an increas

229 ation of intracellular Ca(2+), prevented the stimulation of CTSK expression by RANKL.

230 mpanied by increased ROS generation, and the stimulation of autophagy by rapamycin (Rap) remarkably s

231 cantly reduced GD-induced autophagy, whereas stimulation of autophagy by rapamycin failed to cause an

232 We suggest that trans-stimulation of pol V by RecA bound to ssDNA reflects a d

233 binding loop", ABL) that is critical for the stimulation of ATP hydrolysis by RNA.

234 Stimulation of platelet production by romiplostim may pr

235 ocked alpha-SMA and Fn-ED-A, indicating that stimulation of myofibroblast activation by ROS is downst

236 Additionally, stimulation of glyceroneogenesis by rosiglitazone in adi

237 We have tested the hypothesis that weak stimulation of innate immunity by RSV correlates with in

238 ding to the p53 TAD might be involved in the stimulation of p53 activity by S100 proteins.

239 roblast surface, leading to paracrine growth stimulation of carcinoma cells by Sdc1 ectodomain.

240 This suggests a positive feedback loop of stimulation of chondrocyte hypertrophy by SDF-1/CXCR4, w

241 Stimulation of DNA cleavage by SgrAI, at primary as well

242 feature of diverse human cancers, selective stimulation of proliferation by Shh-proteoglycan interac

243 Therefore, stimulation of microglial clearance by simultaneous acti

244 We propose that chronic stimulation of pDCs by SIV and HIV in non-natural hosts

245 Furthermore FRE exhibited stimulation of glucose uptake by skeletal muscles (hemi-

246 In conclusion, stimulation of A2AR by specific agonists or by increasin

247 Finally, we show that stimulation of ADAM17 by Src(E378G) leads to enhanced pa

248 Stimulation of iNOS by statins via inhibition of geranyl

249 we show that midline exit also requires the stimulation of axon outgrowth by Stem Cell Factor (SCF,

250 This report shows stimulation of MMP1 production by stromal cells via upta

251 glucose uptake and eliminated cis-allostery (stimulation of sugar uptake by subsaturating extracellul

252 ed manner, in which each is required for the stimulation of ATPase activity by substrates.

253 therosclerosis and enhances the inflammatory stimulation of macrophages by suppressing the Akt1-media

254 Stimulation of dendritic cells by T cells activates the

255 ease in the binding of Tea2 and a reciprocal stimulation of Mal3 binding by Tea2 is also observed.

256 ome truncated versions of RAP74, eliminates) stimulation of transcript elongation by TFIIF.

257 The stimulation of GLS1 expression by TGF-beta1 was dependen

258 Stimulation of p300 by TGF-beta was independent of Smads

259 ive effects of TSP-4 on EC may contribute to stimulation of tumor growth by TGF-beta despite the inhi

260 herefore, these studies identified autocrine stimulation of myeloid progenitors by Tgfbeta2 as one me

261 Stimulation of degranulation by thapsigargin, which bypa

262 site on the N terminus that is essential for stimulation of activity by the capacitative entry of Ca(

263 Aldosterone production depends upon stimulation of AS expression by the renin-angiotensin sy

264 The Galphas-dependent stimulation of beating rate by the beta2 adrenergic rece

265 Modest stimulation of catalysis by the full-length Dicer enzyme

266 f HUVEC proliferation but did not affect the stimulation of cells by the heparin-binding domain-delet

267 d assay and provide further evidence for the stimulation of ChlM by the H subunit of magnesium chelat

268 ferences in cellular composition, suggesting stimulation of collagen deposition by the calreticulin-b

269 Stimulation of end resection by the Top3-Rmi1 heterodime

270 We demonstrate that stimulation of GPR17 by the small molecule agonist MDL29

271 The mechanism underlying this event is stimulation of homologous recombination by the pTFO-ICL.

272 quitination mediated by cIAP1 rather than to stimulation of IKKgamma deubiquitination by the deubiqui

273 Stimulation of insulin release by the H454Y GDH mutation

274 Stimulation of insulin secretion by the incretin hormone

275 endent transport on proton coupling, and the stimulation of MsbA-ATPase by the chemical proton gradie

276 Stimulation of NHE3 by the LPA-LPA(5) signaling required

277 on in CTL responses, we investigated whether stimulation of NKG2D by the natural ligand RAE1epsilon w

278 composition ultimately suppresses the CO(2)-stimulation of plant productivity by the third and fourt

279 Stimulation of HBV replication by these agents was linke

280 sociated with ADP accounts for the decreased stimulation of PDK3 activity by these L2 variants.

281 The stimulation of MMP-9 by thrombin was paralleled by an in

282 Stimulation of platelet production by thrombopoietin-rec

283 We found that cyclin E is up-regulated upon stimulation of primary megakaryocytes by thrombopoietin.

284 Stimulation of rRNA synthesis by TIF-IA may therefore pr

285 Taken together, these data indicate that stimulation of peripheral neurons by TLR ligands can ind

286 NF-kappaB show the hBVR role in the initial stimulation of GPBP expression by TNF-alpha-activated NF

287 Upon stimulation of the cells by TNF-alpha, NF-kappaB and TFI

288 Stimulation of TNFR1 by TNFalpha can promote three disti

289 to the C-terminal site is necessary for the stimulation of DNA synthesis by topo I and for the forma

290 A-priming in CD1d-deficient mice or in vitro stimulation of murine hepatocytes by TRAIL but not by TN

291 e provocative hypothesis that the continuous stimulation of thymocytes by TSAbs could lead to a vicio

292 Stimulation of Ras signaling by typical inflammatory sti

293 The stimulation of gate opening by Ub conjugates through Usp

294 Chemical stimulation of the PVN by unilateral microinjections of

295 i knockdown of HSD1 significantly impair the stimulation of hepatic gluconeogenesis by USP2.

296 ds calibrated with field data indicates that stimulation of nitrate uptake by vegetation components u

297 the discovery of a bone conduction-mediated stimulation of the ear by wave propagation in Sechelloph

298 Stimulation of PLC-beta by WNK1 and by Galpha(q) are syn

299 teraction leads to reduction in the in vitro stimulation of BSN cleavage by XerD and a concomitant de

300 FtsK(C)-mediated stimulation of BSN cleavage by XerD requires synaptic co