ライフサイエンスコーパス: non-selective

1 s FFA2-selective, whereas propionate (C3) is non-selective.

2 E) that converted the pore from chloride- to non-selective.

3 inhibitors that are either iNOS-selective or non-selective.

4 In the open state, MscL forms a non-selective 3 nS conductance channel which gates at te

5 have the behavioral toxicity associated with non-selective 5-HT2 receptor agonists, targeting the 5-H

6 c footprint, but the peripheral spread stays non-selective-a surprising finding given a number of ana

7 sorption, while an ultra-thin metal film has non-selective absorption in the near infrared wavelength

8 d with drug-eluting stents may be due to the non-selective actions of antimitogenic drugs on endothel

9 The non-selective adenosine receptor antagonist 8-SPT had no

10 However, in CHU rats, neither the non-selective adenosine receptor antagonist 8-sulphophen

11 s 8-(p-sulfophenyl)-theophylline) (8-SPT), a non-selective adenosine receptor antagonist which has be

12 ird and 8-sulphophenyltheophylline (8-SPT; a non-selective adenosine receptor antagonist) before the

13 (5.0 micromol/kg, i.p.), a centrally active, non-selective adenosine receptor antagonist, attenuated

14 Interestingly, the non-selective agonist, biphalin, exhibited a statistical

15 Among these is the potent, non-selective agonist, FTY720-P, whose mechanism of acti

16 S-21680 (1.0-10.0 micromol/kg, i.p.) and the non-selective agonist, N(6)-ethylcarboximidoadenosine (N

17 sion and neuronal function in vertebrates by non-selective agonistic actions on 5-HT(1) and 5-HT(2) r

18 Similarly, non-selective alpha inhibition with phentolamine increas

19 Selective and non-selective alpha-adrenoceptor antagonism and presynap

20 adrenoceptor antagonist) and phentolamine (a non-selective alpha-adrenoceptor antagonist) were determ

21 himbine (alpha(2)-antagonist), phentolamine (non-selective alpha-antagonist) and bretylium tosylate (

22 Noradrenaline (NA, non-selective alphaAR agonist) constricted 1A, 2A and 3A

23 licits feeding, (2) prior treatment with the non-selective AMPA/KAR antagonist, CNQX, suppresses ATPA

24 Further, LH pretreatment with either the non-selective AMPAR/KAR antagonist, 6-cyano-7-nitroquino

25 s were mainly used to test single compounds, non selective and selective.

26 or many transcription factors are relatively non-selective and found at high frequency within the gen

27 Here we show that psalmotoxin activates non-selective and Na(+)-selective currents in chicken AS

28 (OPG) GEM model, we report novel defects in non-selective and selective attention without an accompa

29 Non-selective and selective cyclo-oxygenase 2 inhibitors

30 r negatively regulate autophagy flux in both non-selective and selective pathways.

31 and more consistently produced than with the non-selective antagonist gabazine, and both were blocked

32 (PET) dopamine subtype 2/3 receptor (D2/3R) non-selective antagonist tracers suggests that obese (OB

33 r dimer population, but the receptor subtype non-selective antagonists atropine and N-methylscopolami

34 A non-selective antimicrobial activity of all ITCs was rev

35 ure of light at 810 nm exhibited minimal and non-selective antimicrobial effects.

36 This was tested using a non-selective AR antagonist, 5-amino-9-chloro-2-(2-furyl

37 Depletion of this essential nutrient induces non-selective autophagy by inhibiting TORC1, leading to

38 and Ssd1, Did4, and others in selective and non-selective autophagy.

39 The variants of the non-selective Bacillus cereus NaK cation channel we exam

40 ee Cl- currents, Xenopus RPE cells exhibit a non-selective background current (Ibkg) which has a line

41 at lower levels of self-administration than non-selective benzodiazepine receptor agonists.

42 zepine receptor partial agonist MRK-696, and non-selective benzodiazepine receptor full agonists, mid

43 ng compounds were compared with those of the non-selective benzodiazepine receptor partial agonist MR

44 ay promote mild bronchodilation that offsets non-selective beta blockade-induced bronchoconstriction

45 Recent experience indicates that combined non-selective beta- and alpha-blockade with carvedilol i

46 n Epac-selective agonist, or isoprenaline, a non-selective beta-adrenergic receptor agonist.

47 s of the beta-adrenergic agents propranolol (non-selective beta-antagonist) and salbutamol (beta(2)-a

48 ts in lesser clinical benefits than combined non-selective beta-blockade with carvedilol at the maxim

49 Propranolol, a non-selective beta-blocker, has been found to have a tre

50 e variability of physicians' preferences for non-selective beta-blockers (BBs) and endoscopic varicea

51 ysine (NTA) and deactivating agents to block non-selective binding between GO-NTA sheets and non-targ

52 tantly, the selective substrates can be made non-selective by insertion of a proline kink at P(3), wi

53 Polycystin-2 (PC2), the PKD2 protein, is a non-selective Ca(2+)-permeable cation channel which may

54 In addition, we show that GLR genes encode non-selective Ca(2+)-permeable channels that can regulat

55 TRPM2 is a non-selective, calcium (Ca(2+))-permeable cation channel

56 Ca(2+)-activated, non-selective (CAN) ion channels sense increases of the

57 show abundant expression of a Ca2+-activated non-selective (CaNS) cation channel.

58 o the activation of undesired C-H bonds by a non-selective catalyst.

59 of extracellular pH (pHo) on calcium-sensing non-selective cation (csNSC) channels in cultured mouse

60 187 (1 microM), to activate Ca(2+)-activated non-selective cation (NSC) channels (T84 cells) and larg

61 of a previously identified calcium activated non-selective cation channel (I(CAN)).

62 The P2X7 receptor is a non-selective cation channel activated by extracellular

63 al vanilloid 1 (TRPV1) is a Ca(2+) permeable non-selective cation channel activated by physical and c

64 rophysiological recordings show that it is a non-selective cation channel and that its activity depen

65 These effects could be prevented with the non-selective cation channel blocker Gadolinium (Gd(3+))

66 The non-selective cation channel blocker Gd(3+) (100 microM)

67 Therefore, opening of a non-selective cation channel causes cell death and Ucn1

68 describe the properties of a Ca2+-permeable non-selective cation channel current that is activated i

69 ET-1 evoked non-selective cation channel currents with a unitary con

70 lt taste receptor is a constitutively active non-selective cation channel derived from the VR-1 gene.

71 ential channel vanilloid type 1 (TRPV1) is a non-selective cation channel expressed in sensory neuron

72 TRPM2 is a calcium-permeable non-selective cation channel expressed in the plasma mem

73 The Mus musculus non-selective cation channel gene mNSC1 was used as a cl

74 bed a constitutively active, Ca2+-permeable, non-selective cation channel in freshly dispersed rabbit

75 ribed a constitutively active Ca2+-permeable non-selective cation channel in freshly dispersed rabbit

76 ctions, to form a heteromeric store-operated non-selective cation channel in HSY cells.

77 al canonical 5 (TRPC5), a calcium-permeable, non-selective cation channel is expressed in the periphe

78 sensitive multistate channels resembling the non-selective cation channel of sea urchin and mouse spe

79 As a non-selective cation channel permeable to Ca(2+) , it tr

80 Pkd2L1 (also called TRPP3) is a non-selective cation channel permeable to Ca(2+), Na(+),

81 4,5-bisphosphate (PtdIns(4,5)P2) -modulated, non-selective cation channel that belongs to the family

82 Transient receptor potential 7 (TRPC7) is a non-selective cation channel that can be activated by bo

83 stin-2 (PC2) is a TRP-type, Ca(2+)-permeable non-selective cation channel that plays an important rol

84 potential vanilloid 1 (TRPv1) receptor is a non-selective cation channel that serves as a marker of

85 Polycystin-2 (PC-2) is a non-selective cation channel that, when mutated, results

86 Localization and function of the polymodal non-selective cation channel TRPV1 (transient receptor p

87 ctance and then activates a Na(+)-permeable, non-selective cation channel via depolarization-induced

88 opening of a cyclic nucleotide-gated (CNG), non-selective cation channel which depolarizes the cells

89 ted that WT ML1 is a multiple subconductance non-selective cation channel whose function is inhibited

90 tery myocytes ET-1 evokes a Ca(2+)-permeable non-selective cation channel with properties similar to

91 that R282E-PepT1 behaved as a peptide-gated non-selective cation channel with the ion selectivity se

92 2l1 or Pkdl), encoding polycystin-L (PCL), a non-selective cation channel, increases neuronal excitab

93 The restricted state is a tetramer non-selective cation channel, whereas the dilated state

94 rat insulinoma cell death by activation of a non-selective cation channel, which leads to irreversibl

95 PC2 is a non-selective cation channel, with multiple subconductan

96 the hexameric construct forms an essentially non-selective cation channel.

97 uppressing K(+) currents and/or activating a non-selective cation channel.

98 melastatin 7 (TRPM7) is a broadly expressed, non-selective cation channel.

99 PC7) functions as a diacylglycerol-activated non-selective cation channel.

100 ) is a receptor-activated, calcium permeant, non-selective cation channel.

101 een shown to function as a Ca(2+)-permeable, non-selective cation channel.

102 as Ca(2+)-activated Cl() channels (CaCC) and non-selective cation channels (NSCC) have been suggested

103 ndependent rapidly activating Ca2+-permeable non-selective cation channels (NSCCs).

104 act with and regulate members of a family of non-selective cation channels (TRPC) which have been sug

105 P2X receptors are trimeric, non-selective cation channels activated by ATP that have

106 tively, and E(r) values indicated that these non-selective cation channels are highly permeable to Ca

107 ents, and families - which included putative non-selective cation channels for the NaCl treatment and

108 linoma cells and suggest that this family of non-selective cation channels has a widespread distribut

109 RPC4 proteins function as Ca(2+) conducting, non-selective cation channels in endothelial, smooth mus

110 transient receptor potential (TRP) family of non-selective cation channels in murine megakaryocytes f

111 tion-activated cyclic nucleotide-gated (HCN) non-selective cation channels in neurons carry currents

112 f the transient receptor potential family of non-selective cation channels is a polymodal nociceptor.

113 egarding Cl(-) channels in the ER/SR and the non-selective cation channels or putative 'Ca(2+) leak c

114 regarding Cl- channels in the ER/SR and the non-selective cation channels or putative 'Ca2+ leak cha

115 Activation of Ca2+-permeable non-selective cation channels produces an increase in ex

116 ogical and pharmacological properties of the non-selective cation channels stimulated by the physiolo

117 Murine ICC express Ca(2+)-inhibited, non-selective cation channels that are periodically acti

118 (TRP channel (TRPC) 1-7 are Ca(2+)-permeant, non-selective cation channels that are widely expressed

119 d-aspartate (NMDA) receptors are heteromeric non-selective cation channels that require the binding o

120 ntial (TRP) superfamily comprises a group of non-selective cation channels that sense and respond to

121 (TRPM7) channels are novel Ca(2+)-permeable non-selective cation channels ubiquitously expressed.

122 ) channels, as well as a class of excitatory non-selective cation channels, TRPM2.

123 Here, we ask whether non-selective cation channels, which share an overall st

124 f the transient receptor potential family of non-selective cation channels.

125 e mammalian central nervous system and gates non-selective cation channels.

126 e C-dependent events activate Ca2+-permeable non-selective cation channels.

127 L) proteins belong to the TRP superfamily of non-selective cation channels.

128 extracellular Ca(2+); (ii) large conductance non-selective cation channels; and (iii) Ca(2+)-dependen

129 ing a constitutively active Ca(2+)-permeable non-selective cation conductance (I(cat)) in rabbit ear

130 cid, an antagonist for the calcium-activated non-selective cation conductance (ICAN ) abolished the e

131 One group of ICC expressed a basal non-selective cation conductance (NSCC) that was inhibit

132 (GSK), a TRPV4 channel agonist, activated a non-selective cation conductance that coupled to activat

133 to a Ca(2+)-inhibited, voltage-independent, non-selective cation conductance that has similar proper

134 This is accompanied by up-regulation of a non-selective cation conductance with TRPM4-like propert

135 mic acid, a blocker of the calcium-activated non-selective cation conductance, abolished the effect o

136 to a voltage-independent, Ca(2+)-regulated, non-selective cation conductance.

137 In smooth muscle, non-selective cation conductances contribute to agonist-

138 s the cell by recruiting a calcium-activated non-selective cation current (ICAN) capable of generatin

139 rtal vein myocytes noradrenaline activates a non-selective cation current (Icat) which involves a tra

140 , as well as a mechanically-sensitive inward non-selective cation current characteristic of Piezo2.

141 of cells expressing TRPC1+STIM1 activated a non-selective cation current, I(SOC), that was blocked b

142 -acetyl-sn-glycerol (OAG) stimulated similar non-selective cation currents and Ca2+ entry in HSY cell

143 ading to the postulation that post-traumatic non-selective cation currents are determined by TRPM4/SU

144 cells, arginine-vasopressin (AVP) activated non-selective cation currents associated with TRPC6 acti

145 PKD2-null cells can confer Ca(2+)-permeable non-selective cation currents.

146 These currents are produced by relatively non-selective, cation-permeable channels or pores in the

147 ezo proteins as subunits of Ca(2+)-permeable non-selective cationic channels for detection of noxious

148 ponsible for flow-sensitive non-inactivating non-selective cationic channels which depolarize the mem

149 rrent, and activation of a calcium-dependent non-selective cationic current (ICAT).

150 n decrease unitary conductance and produce a non-selective channel while the presence of a positive c

151 nt MPV17 to reveal that this protein forms a non-selective channel with a pore diameter of 1.8 nm and

152 of Ca(2+) through the self-contained cation non-selective channel.

153 The non-selective classical PKC inhibitor Go6976 inhibited a

154 state duplication frequencies measured under non-selective conditions (10(-4) to 10(-5) ) confirmed t

155 T-DNA target sites identified using non-selective conditions did not correlate with DNA meth

156 of genomic sequences targeted by T-DNA under non-selective conditions were similar to those of random

157 ng T-DNA/plant DNA junctions generated under non-selective conditions.

158 restin itself possesses a stretch-sensitive, non-selective conductance that is largest in the presenc

159 tracellular chloride is a stretch-sensitive, non-selective conductance within the lateral membrane, G

160 t of BK channels but dependent on background non-selective conductances.

161 t of BK channels but dependent on background non-selective conductances.

162 A non-selective COX inhibitor (indomethacin, 15 mg kg(-1)

163 eatment of APP-overexpressing cells with the non-selective COX inhibitor ibuprofen (1 microM, 48 h) o

164 ol), a non-specific NO synthase inhibitor, a non-selective COX inhibitor or combined inhibition durin

165 roup subset received 100 mg of indomethacin (non-selective COX-1 and COX-2 inhibitor), and another HS

166 rising from a defined pilin progenitor under non-selective culture conditions.

167 Here, we described an outward rectifying non-selective current mediated by a TRP ion channel in i

168 lia also revealed TRPM4-like, Ca2+-activated non-selective currents (I CAN) with an EC50 of 1.2 micro

169 G-monomethyl-l-arginine (l-NMMA, 10 mm), the non-selective cyclooxygenase inhibitor ketorolac trometh

170 clooxygenase-2 inhibitor) or indomethacin (a non-selective cyclooxygenase inhibitor) had significant

171 Autophagy is primarily considered a non-selective degradation process induced by starvation.

172 ide, whereas the aversive one functions as a non-selective detector for a wide range of salts.

173 prises hydrophobic interactions that provide non-selective dimerization affinity.

174 This non-selective divalent activation is in contrast with th

175 diversity set, and the selective drugs from non-selective drugs.

176 e during sessions with good avoidance but is non-selective during poor avoidance, with high release c

177 Non-selective (e.g. non-steroidal anti-inflammatory drug

178 Furthermore, a non-selective endocytosis inhibitor, concanavalin A, inh

179 1F, in the squash protein converts it from a non-selective enzyme into a selective one.

180 iation, suggesting a binding site relatively non-selective for small cations.

181 We speculate that this "non-selective" form of mitophagy may potentially help to

182 shed that discriminate between selective and non-selective forms of the enzyme.

183 The non-selective GABAAR PAM triazolam and the alpha1GABAA p

184 subtypes in the memory-impairing effects of non-selective GABAAR PAMs has not been fully elucidated.

185 are primarily involved in the impairment, by non-selective GABAAR PAMs, of visual recognition and vis

186 The non-selective GAT blocker nipecotic acid (100-300 microM

187 The non-selective glutamate reuptake antagonist, threo-beta-

188 howing efficacy of sarcosine, an endogenous, non-selective glycine-reuptake inhibitor mediated by Gly

189 ntify the benzodiazepine drug lorazepam as a non-selective GPR68 positive allosteric modulator.

190 mic position did not affect reversion during non-selective growth.

191 (intrathecal) injection of carbenoxolone (a non-selective hemichannel blocker) and selective connexi

192 er sos1 mutants more tolerant to paraquat, a non-selective herbicide causing oxidative stress, indica

193 ustained bradycardia induced by S1P receptor non-selective immunosuppressive agonists in wild-type mi

194 ugh the E1224A mutant has full activity in a non-selective in vitro transcription assay, it is temper

195 two hypotheses: that stress would lead to a non-selective increase in the expression of Pavlovian bi

196 cker, improves the clinical outcome, whereas non-selective inhibition of both forms of tumour necrosi

197 e of PDE7A1 catalytic domain in complex with non-selective inhibitor 3-isobutyl-1-methylxanthine and

198 portion of posterior telencephalon receives non-selective, interspersed inputs from all glomeruli, w

199 Mutations appear during non-selective intracellular replication, and the frequen

200 nt receptor potential ankyrin 1 (TRPA1) is a non-selective ion channel, which is expressed in nocicep

201 ular, monovalent cation transporters such as non-selective ion channels and cation:proton antiporters

202 hannels defines a new family of functionally non-selective ion channels, and also provides important

203 meric preparations form voltage-independent, non-selective ion channels.

204 In addition, W1531G created a second non-selective ion-conducting pore, bypassing the outer v

205 BA(A) receptor agonist) or kynurenic acid (a non-selective ionotropic glutamate receptor antagonist)

206 However, G5, a non-selective isopeptidase inhibitor, triggers a distinc

207 Preincubation with a non-selective JAK inhibitor restored glucose uptake and

208 Glibenclamide, a non-selective K(ATP) channel blocker, was used to furthe

209 Either the non-selective K(ATP) channel closer glibenclamide or the

210 ed as a weak (EC(50) = approximately 10 mum) non-selective K+ channel blocker.

211 otein dynamics (flexibility) and/or a simple non-selective kinetic mechanism.

212 Here we show how selective and non-selective lysosomal protein degradation pathways coo

213 r peripheral adverse effects associated with non-selective mAChR agonists.

214 sphingosine 1-phosphate (S1P) receptors in a non-selective manner decreases disease activity in patie

215 The samples were enumerated on selective and non-selective media and on doxycycline (4 microg/ml) med

216 (MT-II), a cyclic heptapeptide, is a potent, non-selective melanocortinergic agonist.

217 cterisation of a novel group of functionally non-selective members of the prokaryotic 'inward rectifi

218 Local infusion of a non-selective mGlu2/3 agonist, LY379268, in the reticula

219 The non-selective mGluR antagonist MCPG produced a dose-depe

220 tamate receptor mGluR5) and 10 mum LY341495 (non-selective mGluR blocker), but not by 80 mum AP5 (NMD

221 epths, implying that reconstructions using a non-selective mixture of morphotypes could potentially b

222 allenges that have limited previously tested non-selective MMP inhibitors.

223 al effects may be accomplished by apparently non-selective modulators.

224 Indatraline is an antidepressive agent and a non-selective monoamine transporter inhibitor that block

225 ure of resistance to seizures induced by the non-selective muscarinic agonist pilocarpine.

226 nwanted peripheral responses associated with non-selective muscarinic agonists.

227 The EC and SMC are coupled via non-selective myoendothelial gap junctions (MEGJs) which

228 A non-selective N-methyl-d-aspartate receptor (NMDAR) anta

229 Local infusion of the non-competitive non-selective nAChR antagonist mecamylamine or viral-med

230 Our results demonstrate that the non-selective NaK2CNG still retains a K(+)-selective sit

231 -selective NaK2K mutant and the other is the non-selective NaK2CNG, a CNG channel pore mimic.

232 Because deficiency of sodium leak channel, non-selective (Nalcn) causes lethal apnea in humans and

233 ssense mutations in the sodium leak channel, non-selective (NALCN) in four families affected by CLIFA

234 l lobe and type II neuroblasts compared with non-selective neuroblasts, neurons and glia revealed a r

235 It has been shown that the non-selective nicotinic agonist nicotine has an influenc

236 cotinic antagonist methyllycaconitine or the non-selective nicotinic antagonist mecamylamine indicate

237 after intra-peritoneal administration of the non-selective nitric oxide synthase (NOS) inhibitor, N(G

238 tension as does systemic administration of a non-selective nitric oxide synthase (NOS) inhibitor.

239 lation, which was only partially reversed by non-selective NO synthase inhibition.

240 ad any of three clinically important errors: non-selective non-steroidal anti-inflammatory drugs (NSA

241 Cyclo-oxygenase-2 selective inhibitors and non-selective non-steroidal anti-inflammatory drugs (NSA

242 uld reduce ulcer complications compared with non-selective non-steroidal anti-inflammatory drugs, but

243 nitro-l-arginine methyl ester hydrochloride (non-selective NOS inhibitor); (3) 5 mm N-propyl-l-argini

244 While non-selective NOS inhibitors are neuroprotective, the ro

245 ved following the systemic administration of non-selective NOS inhibitors, and thus provides support

246 CVC at eNOS-inhibited (41 +/- 3%CVCmax) and non-selective NOS-inhibited (40 +/- 4%CVCmax) sites were

247 was no difference between eNOS-inhibited and non-selective NOS-inhibited sites.

248 cantly less likely to have been prescribed a non-selective NSAID if they had a history of peptic ulce

249 2 inhibitors and aspirin than in those using non-selective NSAIDs and aspirin; significantly fewer un

250 sion that COX-2 inhibitors are preferable to non-selective NSAIDs in patients with chronic pain and c

251 exposure to cyclo-oxygenase 2 selective and non-selective NSAIDs was compared with remote exposure t

252 The non-selective NSAIDs, ibuprofen and naproxen, and a sele

253 ointestinal benefits of COX-2 inibitors over non-selective NSAIDs.

254 l blood loss with COX-2 inhibitors than with non-selective NSAIDs.

255 with different selective drugs in respect to non-selective ones, most of them are only able to delay

256 Rats pretreated with the non-selective opioid antagonist naltrexone (1.25-3.75 mi

257 The non-selective opioid antagonist, naloxone, returned the

258 The purpose of this study was to assess a non-selective opioid receptor agonist, biphalin, in decr

259 cts were attenuated by pretreatment with the non-selective opioid receptor antagonist naloxone.

260 ile, intrathecal pretreatment with naloxone, non-selective opioid receptor antagonist, did not affect

261 lunteers using PET and [11C]diprenorphine, a non-selective opioid receptor radioligand.

262 xpressed human rod opsin, driven by either a non-selective or ON-bipolar cell-specific promoter, can

263 neable feature that is bestowed on otherwise non-selective ORAI1 channels by STIM1.

264 We suggest, therefore, that so-called non-selective oxygen is capable of insertion into carbon

265 Our data suggest that claudin-16 forms a non-selective paracellular cation channel, rather than a

266 n effect replicated pharmacologically with a non-selective PDE4 inhibitor, implicating cAMP signaling

267 The effects of non-selective (PGE2 , misoprostol), EP2 -selective (ONO-

268 4 evolved by recruitment and adaptation of a non-selective phosphodiesterase and a matrix component i

269 sive "designer" theophylline, the archetypal non-selective phosphodiesterase inhibitor.

270 oocytes in a manner consistent with a large non-selective pore.

271 Non-selective positive allosteric modulators (PAMs) of G

272 tide inhibitor of calcineurin (CaN-AIP); the non-selective PP1/PP2A inhibitors okadaic acid (0.5, 10,

273 In crystal structures of the non-selective PPP1R15B-PP1G complex, the functional core

274 smolytes, proposedly due to the opening of a non-selective protein channel of unknown molecular ident

275 Staurosporine, a non-selective protein kinase inhibitor, shifted the acti

276 duced inhibition of EPSCs was reduced by the non-selective protein kinase inhibitors H-7 (100 microM)

277 ical analyses imply that CsgG is an ungated, non-selective protein secretion channel that is expected

278 nal poly(IC) exposure and treatment with the non-selective purinergic antagonist suramin to test the

279 Non-selective purinergic receptor antagonists (pyridoxal

280 ses of which have been marred by late-stage, non-selective RCM.

281 ockade of CRH receptors in the mPFC with the non-selective receptor antagonist d-Phe-CRH (50 ng or 10

282 Non-selective Runx2(+/-) mice, which have an equivalent

283 Inhibition of lymphocyte recirculation by non-selective S1P receptor agonists produces clinical im

284 Our results are consistent with a non-selective secretion model for most microRNAs, althou

285 For patients taking non-selective serotonin reuptake inhibitor antidepressan

286 ght a slight shift in prescribing toward the non-selective serotonin reuptake inhibitor bupropion hyd

287 ory, unintended declines in case finding and non-selective serotonin reuptake inhibitor substitute tr

288 Lysergic acid diethylamide (LSD) is a non-selective serotonin-receptor agonist that was first

289 single divalent metal-binding site which is non-selective, since Mn2+, Co2+ and Zn2+ compete with Mg

290 oietic cells to relatively Ca2+-selective or non-selective SOC channels in other cells.

291 rovides a structural basis for selective and non-selective substrate recognition by MT1-MMP.

292 entire catalytic pocket of MT1-MMP, whereas non-selective substrates are kinked at the conserved P(3

293 s, with only a minor effect on hydrolysis of non-selective substrates.

294 single molecule selectivity, referred to as non-selective switching.

295 s of the NaK channel from Bacillus cereus, a non-selective tetrameric cation channel, in its Na+- and

296 Mammalian non-selective transient receptor potential cation channe

297 The non-selective Transient Receptor Potential Melastatin 4

298 in DRG neurones, which was attenuated by the non-selective TRP channel antagonist ruthenium red (10 m

299 r corresponding lactones (CQALs, FQALs) in a non-selective way.

300 Administration of the relatively non-selective Y receptor antagonist PYX-2 or the selecti