ライフサイエンスコーパス: serotonin receptor

1 re transfected with 14 different isoforms of serotonin receptor.

2 in releasing hormone receptor, and the 5HT1a serotonin receptor.

3 tes, and modulates signaling of the 5-HT(2A) serotonin receptor.

4 cell surface through an as yet unidentified serotonin receptor.

5 istidine sensor kinase, CpxA, is a bacterial serotonin receptor.

6 er insect amine receptors and the vertebrate serotonin receptors.

7 BST, and of neuron populations that express serotonin receptors.

8 functions and behavior by directly targeting serotonin receptors.

9 ly members for its interactions with defined serotonin receptors.

10 hich tryptamine-related agents bind at 5-HT6 serotonin receptors.

11 e polyomavirus and SV40, while JC virus uses serotonin receptors.

12 circuits are modulated via several different serotonin receptors.

13 of GABA-positive neurons are associated with serotonin receptors.

14 mRNAs, including the mRNAs of glutamate and serotonin receptors.

15 purposes, particularly in the modulators of serotonin receptors.

16 As, including the pre-mRNAs of glutamate and serotonin receptors.

17 cular explanation for LSD's actions at human serotonin receptors.

18 arinic M1 and M3, neurokinin, opioid KOP and serotonin receptors.

19 raphe nuclei, and expresses high density of serotonin receptors.

20 nge eating, and the contribution of specific serotonin receptors.

21 wo serotonin-related gene polymorphisms, the serotonin receptor 1A (5-HT1A) polymorphism at -1019C>G

22 Activation or inhibition of serotonin receptor 1A (5-HTR1A) recapitulated or abolish

23 Administration of the serotonin receptor 1A partial agonist buspirone prevente

24 (miR135), and both serotonin transporter and serotonin receptor-1a transcripts.

25 arge family of S100 proteins, interacts with serotonin receptor 1B (5-HTR1B), modulates 5-HT1B recept

26 by serotonin, acting through the Drosophila serotonin receptor 1B (d5-HT1B).

27 Furthermore, pharmacological inhibition of serotonin receptor 1B with SB224289, and of receptor 2A

28 d agonists for members of the 5-HT2 class of serotonin receptors, 2,5-dimethoxy-4-iodoamphetamine (DO

29 We show that the serotonin receptor 2A (5-HT(2A)), a prototypical GPCR in

30 Upregulation of the serotonin receptor 2A (5-HT(2A)R) in dorsal horn neurons

31 hoxy-4-iodoamphetamine (DOI), an agonist for serotonin receptor 2A (5-HT2AR).

32 and identified tryptophan hydroxylase (Trh), serotonin receptor 2a (5HT2a), and the solute carrier 7-

33 xplored the roles of two of these receptors, serotonin receptor 2A (5HTR2A) and the D4 dopamine recep

34 ound that adrenoceptor alpha 2C (Adra2c) and serotonin receptor 2a (Htr2a) were the most highly expre

35 ms in the monoamine oxidase A (MAOA-LPR) and serotonin receptor 2A genes (rs6314) moderated the effec

36 Editing of the pre-mRNA for the serotonin receptor 2C (5-HT2CR) by site-specific adenosi

37 (SCI) leads to a decrease in mRNA editing of serotonin receptor 2C (5-HT2CR) contributing to post-SCI

38 nd decreased dopamine receptor D2 (DRD2) and serotonin receptor 2C (HTR2C) expression in the ventral

39 The serotonin receptor 2C plays a central role in mood and a

40 I-52 changes the alternative splicing of the serotonin receptor 2C pre-mRNA, which is different from

41 tophan hydroxylase 1 (Tph1, rs262731280) and serotonin receptor 3A (Htr3a, rs50670893) were associate

42 Noncoding variants in 5-hydroxytryptamine (serotonin) receptor 4 (HTR4) are associated with pulmona

43 affinity agonist of the 5-hydroxytryptamine (serotonin) receptor 4 that enhances motility in the gast

44 on occurred primarily through stimulation of serotonin receptor 5-HT(1A).

45 tions in editing and alternative splicing of serotonin receptor 5-HT(2C) transcripts.

46 P, calcitonin-gene related peptide, and the serotonin receptor 5-HT(3)R.

47 we demonstrated that LK neurons express the serotonin receptor 5-HT1B .

48 shown to be independent of their function as serotonin receptor 5-HT1B/1D agonist or cytostatic drug,

49 s for each of these receptors and found that serotonin receptor 5-HT2A is the sole molecular target f

50 l structure of LSD in complex with the human serotonin receptor 5-HT2B.

51 n is a peripherally active antagonist of the serotonin receptor 5-HT3, and is marketed for prevention

52 monoamine oxidase A (serotonin catabolism), serotonin receptor 5-HT4, or mouse serotonin transporter

53 lactoseries tetrasaccharide c (LSTc) and the serotonin receptor 5-hydroxytryptamine (5-HT) receptor 5

54 Preclinical evidence implicates the serotonin receptor 5-hydroxytryptamine 1B (5-HT1B) in th

55 for serotonin biosynthesis in the brain-and serotonin receptor 5-hydroxytryptamine receptor 6 (HTR6)

56 Expression of the G alpha(q)-linked serotonin receptor 5-hydroxytryptamine receptor-2b (Htr2

57 Constitutive activity of the serotonin receptors 5-HT2B/C is required for the develop

58 Several studies have shown that the serotonin receptors 5-HTR1b and 5-HTR4 play key roles in

59 reversal of hypothalamic NPY, alpha-MSH, and serotonin receptor (5-HT(1B)-receptor) enhancing FI.

60 Serotonin receptor (5-HT(3A)R) is the most common therap

61 n reuptake transporter (SERT) and the type 7 serotonin receptor (5-HT(7)) were expressed in human and

62 [11C]CUMI-101 is the first selective serotonin receptor (5-HT1AR) partial agonist radiotracer

63 li (noc), and confirmed that Ftz regulates a serotonin receptor (5-HT2).

64 ypes: alpha7-nAChR, alpha4beta2-nAChR, and a serotonin receptor (5-HT3AR), along with a fluorescent r

65 y with CA1 pyramidal cells via activation of serotonin receptors (5-HT(1B)Rs), without affecting near

66 5-HT(2)-type serotonin receptors (5-HT(2)Rs) are widely expressed thr

67 Serotonin receptors (5-HT(3A)R) play a crucial role in r

68 A new homology model of type-3A serotonin receptors (5-HT(3A)Rs) was built on the basis

69 se to 5-hydroxytryptamine (5-HT), the type 1 serotonin receptors (5-HT1Rs) preferentially couple to t

70 Expression of serotonin receptors (5-HTR), transporter (5-HTT), and tr

71 emical localization of the crustacean type 1 serotonin receptor, 5-HT1crust, throughout the crayfish

72 The ionotropic serotonin receptor, 5-HT3 , is expressed by many develop

73 tors, we have cloned and fully sequenced two serotonin receptors, 5-HT(1Mac) and 5-HT(2Mac), from the

74 cocorticoid receptor (GR) and an increase in serotonin receptor 5HT-1a, consistent with the decreased

75 tropic glutamate receptors, GluR2-6, and the serotonin receptor, 5HT2C.

76 The serotonin receptor 5HT2CR pre-mRNA is subject to adenosi

77 ncluding somatostatin receptor 3 (Sstr3) and serotonin receptor 6 (Htr6), localize to cilia.

78 ansport of two different cargoes (membranous serotonin receptor 6-green fluorescent protein [HTR6-GFP

79 mine (5-HT)), and we found that knockdown of serotonin receptor-6 (5-Htr6) expression or pharmacologi

80 imal studies have shown that knockout of the serotonin receptor 7 gene (HTR7) resulted in an antidepr

81 E2 series prostaglandins and DHA influences serotonin receptor action by increasing cell membrane fl

82 tion, the intracellular signal mediating the serotonin receptor action in cholangiocytes was characte

83 nerve activity has been reported to require serotonin receptor activation and protein syntheses.

84 We conclude that phrenic LTF requires spinal serotonin receptor activation and protein synthesis.

85 hat LTF of phrenic amplitude requires spinal serotonin receptor activation and spinal protein synthes

86 Serotonin receptor activation by serotonin showed a simi

87 5-HT(2A) (Q pathway) and 5-HT(7) (S pathway) serotonin receptor activation cancels phrenic motor faci

88 Intermittent spinal serotonin receptor activation elicits long-lasting phren

89 pLTF requires spinal serotonin receptor activation, new BDNF synthesis and Tr

90 In the case of serotonin, receptor activation rates varied with agonist

91 syndrome patients with a clinically-approved serotonin receptor agonist (lorcaserin, Belviq(R)) and o

92 opropan-1-ol (6), an analogue of the 5-HT(2) serotonin receptor agonist 1-(4-bromo-2,5-dimethoxypheny

93 Psilocybin is a serotonin receptor agonist that occurs naturally in some

94 ase inhibitor) and pergolide (a dopamine and serotonin receptor agonist) robustly reduced alcohol int

95 ith 5-nonyloxytryptamine (5-NT), a prototype serotonin receptor agonist, diminished reovirus cytotoxi

96 c acid diethylamide (LSD) is a non-selective serotonin-receptor agonist that was first synthesized in

97 ment for menstrual migraine is inconsistent, serotonin receptor agonists (triptans) provide acute rel

98 Observed effects of serotonin receptor agonists and antagonists in abdomen p

99 uts onto IO cells are strongly suppressed by serotonin receptor agonists as well as release of endoge

100 Because 5-HT(2A) serotonin receptor agonists might also produce undesirab

101 rain, attempts were made to identify 5-HT(2) serotonin receptor agonists with reduced propensity to p

102 g development and injury, and is promoted by serotonin receptor agonists.

103 of osteoblast numbers because inhibition of serotonin receptors alone in leukemic blasts did not aff

104 We immunized mice with the rat 5HT2c serotonin receptor and derived clonal hybridoma cells, w

105 vatives as selective inhibitors of the 5-HT6 serotonin receptor and the TRPV1 ion channel.

106 Dopamine and serotonin receptor and transporter genes have been an ea

107 These include drugs that act on the serotonin receptor and transporter system: antidepressan

108 acts with 5-hydroxytryptamine(2A) (5-HT(2A)) serotonin receptors and attenuates receptor signaling vi

109 in bioavailability alters gene expression of serotonin receptors and immune-related genes.

110 We demonstrate that clemizole binds to serotonin receptors and its antiepileptic activity can b

111 imaging-based human brain atlas of important serotonin receptors and the transporter.

112 st notably, we found changes in dopamine and serotonin receptors and transporters (Dat1, Drd4, 5Htt,

113 istent both with the known actions of LSD on serotonin receptors and with limited evidence that highe

114 ndent substituents, certain receptors (e.g., serotonin receptors) and monoamine transporters (i.e., s

115 vine peripheral leukocytes express all known serotonin receptors, and can synthesize, uptake and degr

116 The prototypical hallucinogen LSD acts via serotonin receptors, and here we describe the crystal st

117 00A10 (p11) was identified as a regulator of serotonin receptors, and it has been implicated in the e

118 nosine residues in a subset of glutamate and serotonin receptors, and this editing results in protein

119 The distribution of LSTc, serotonin receptors, and virus binding sites overlapped

120 s are compared with those obtained following serotonin receptor antagonism or episodic carotid sinus

121 1 receptor antagonists (NK1-RAs) and the new serotonin receptor antagonist (5HT3-RA) palonosetron.

122 A broad-spectrum serotonin receptor antagonist (methysergide) or protein

123 longer recommends the combination of a 5-HT3 serotonin receptor antagonist and dexamethasone for the

124 SSRI fluoxetine and fluvoxamine and the 5-HT serotonin receptor antagonist cyproheptadine were conduc

125 nsulin receptor, or pharmacologically by the serotonin receptor antagonist cyproheptadine.

126 icated healthy comparison women received the serotonin receptor antagonist metergoline as part of a d

127 ytryptamine affects phosphate excretion, the serotonin receptor antagonist methiothepin (20 microgram

128 The bilateral administration of the serotonin receptor antagonist methysergide (2.5 microg,

129 or depotentiation, by DSI was blocked by the serotonin receptor antagonist methysergide and mimicked

130 Furthermore, the serotonin receptor antagonist methysergide blocked this

131 ere occluded by serotonin and blocked by the serotonin receptor antagonist methysergide, suggesting t

132 Spinal methysergide, a serotonin receptor antagonist, blocked apnoea-induced LT

133 ination of a 5-hydroxytryptamine-3 (5-HT(3)) serotonin receptor antagonist, dexamethasone, and aprepi

134 ), dexamethasone, and dolasetron mesylate, a serotonin receptor antagonist.

135 Hairless mice were injected with PAF or serotonin receptor antagonists and then exposed to solar

136 Type 2 and 3 serotonin receptor antagonists attenuated serotonin's po

137 Also, the PAF and/or serotonin receptor antagonists blocked skin cancer progr

138 eatment of mammary epithelial membranes with serotonin receptor antagonists increased their transepit

139 Serotonin receptor antagonists may thus be useful in the

140 Pretreatment with the serotonin receptor antagonists methysergide (4 mg/kg, i.

141 Although serotonin receptor antagonists remain key in the multimo

142 ed as an affinity matrix in the screening of serotonin receptor antagonists with known affinities for

143 The PAF and serotonin receptor antagonists worked in a synergistic f

144 atients intolerant of or refractory to 5-HT3 serotonin receptor antagonists, neurokinin-1 receptor an

145 polarization of neutrophils, suggesting that serotonin-receptor antagonists or serotonin reuptake inh

146 gy" and discuss how drugs targeting specific serotonin receptors are beginning to help treat a wide r

147 nervous system, and virtually all of the 15 serotonin receptors are expressed outside as well as wit

148 5-Hydroxytryptamine 2A (5-HT(2A)) serotonin receptors are important for a variety of funct

149 In addition to LSTc, type 2 serotonin receptors are required for facilitating virus

150 5-HT(2A) serotonin receptors are unusual among G-protein coupled

151 ychological processes, and drugs that target serotonin receptors are used widely in psychiatry and ne

152 are mediated through specific histamine and serotonin receptors, are independent of VEGF-A, and are

153 Antipsychotic drugs target dopamine and serotonin receptors as well as Kv11.1 potassium channels

154 Because PCA 4248 also blocks serotonin receptor binding, we measured the effect that

155 riction was largely antagonized by selective serotonin receptor blockade, with little further antagon

156 the functional activity of not only 5-HT(2A) serotonin receptors but also selected Galpha(q)-coupled

157 s effect through the specific binding to the serotonin receptor, but recent research has suggested th

158 sulfonamides, sulfones) bind at human 5-HT6 serotonin receptors, but it has been difficult relating

159 regulate the expression of Htr2c, one of the serotonin receptors, by binding to its promoter, and the

160 -length N-acetylated peptides from the 5HT2c serotonin receptor C-terminal sequence, as well as for o

161 in systems and may play an etiologic role in serotonin receptor changes observed in patients with maj

162 ge of recent findings demonstrating that the serotonin receptor chaperone, p11, is an important molec

163 Canonical serotonin receptor compounds have given way to a myriad

164 Competition binding assays at several serotonin receptors confirmed that an N-arylmethyl subst

165 hment receptor for JCPyV and that the type 2 serotonin receptors contribute to JCPyV infection by fac

166 However, variation in genes encoding serotonin receptors could also explain antidepressant si

167 es, such as D2 dopamine receptors and 5-HT2A serotonin receptors, could evolve a mechanism that discr

168 Although serotonin receptor density is greatest in brain regions

169 uate their long-term effects on dopamine and serotonin receptors density in different brain areas.

170 sma induced neutrophil CXCR4 expression in a serotonin-receptor-dependent manner.

171 A) receptors in cells stably expressing this serotonin receptor did not alter cGMP levels.

172 While the expression of the serotonin receptors did not show a significant relations

173 n no reports demonstrating the expression of serotonin receptor dimers/oligomers on the plasma membra

174 The study provides valuable insight into serotonin receptor (dys)function in a limbic brain area.

175 Two different forms of the 5-HT(3) serotonin receptor, each with a different desensitizatio

176 affects diarrhea and anxiety via effects on serotonin receptors, enhanced intestinal repair, and sod

177 Thus, serotonin receptor-evoked facilitatory actions are compl

178 meric GABArho1, alpha7 nicotinic, and 5-HT3A serotonin receptors expressed in Xenopus oocytes.

179 pressing GABAergic interneurons, a subset of serotonin receptor-expressing interneurons.

180 s are needed to determine whether postmortem serotonin receptor findings are also present in vivo and

181 homomeric 5-hydroxytryptamine 3A (5-HT(3A)) serotonin receptor for 15 to 20 mus to demonstrate that

182 LTF is serotonin dependent, and the relevant serotonin receptors for phrenic LTF are located in the c

183 llular expression patterns of the Drosophila serotonin receptor gene family.

184 he regulation of alternative splicing of the serotonin receptor gene in humans and other mammals.

185 st strongly in the amygdala, but none of the serotonin receptor genes, were predictive of interindivi

186 dopamine receptor (Gs-coupled) and the 5HT1E serotonin receptor (Gi-coupled) mediated cellular prolif

187 gents, which block postsynaptic dopamine and serotonin receptors, have advantages over traditional an

188 rtex of Phf8 deficient mice and identify the serotonin receptors Htr1a and Htr2a as direct targets of

189 on of the serotonin transporter (SLC6A4) and serotonin receptor (HTR1A, HTR2A, HTR2C) genes with anxi

190 in and its receptor, estrogen receptor beta, serotonin receptors (Htr1a, Htr2a) and glutamate recepto

191 We demonstrate that the serotonin receptor htr2a is expressed on these commissur

192 We find that the serotonin receptor HTR2A selectively activates radial gl

193 erstood, although activation of the 5-HT(2A) serotonin receptor (HTR2A) is key.

194 ilution phenotype was also observed with the serotonin receptor Htr6, fibrocystin PKHD1, and Arl13b.

195 This survey led to the discovery of the serotonin receptor HTR7 as a key mediator of serotonergi

196 ng, presumably through its action on various serotonin receptors (HTRs).

197 on of a dopamine receptor effectively into a serotonin receptor illustrates the plasticity of GPCR si

198 onclusion, 5-HT7 receptor is a novel type of serotonin receptor implicated in hepatocyte proliferatio

199 plicated the 5-hydroxytryptamine 2B (5-HT2B) serotonin receptor in mediating the heart valve fibropla

200 For activating pumping, the SER-7 serotonin receptor in the MC motor neurons in the feedin

201 The finding that ergotamine binds serotonin receptors in a less conserved extended binding

202 Antipsychotic compounds bind at serotonin receptors in human prefrontal cortex.

203 To further define the roles of serotonin receptors in infection, HEK293A cells, which a

204 These findings suggest an important role of serotonin receptors in mediating the discriminative stim

205 This study aimed to determine levels of two serotonin receptors in subtypes of vascular dementia and

206 Postmortem studies of serotonin receptors in suicides localize changes to the

207 d to study the relationship between GABA and serotonin receptors in the central nucleus of the rat in

208 We studied the role of adrenergic and serotonin receptors in the generation of superoxide by r

209 roxytryptamine (5-HT) 2A (5-HT2A) and 5-HT2C serotonin receptors in the hypothalamus were altered by

210 e differential roles of distinct families of serotonin receptors in this process and propose that reg

211 rally and directly activates SER-7, a type 7 serotonin receptor, in MC motor neurons in the feeding o

212 found that omega-3 fatty acids could prevent serotonin receptor-induced MAPK activation in hippocampa

213 -dependent pMF, which was enhanced by spinal serotonin receptor inhibition.

214 The association between selective serotonin receptor inhibitors (SSRIs) and risk of upper

215 Selective serotonin receptor inhibitors are prescribed to reduce t

216 Consistent with a role for spinal 5-HT(3) serotonin receptors, intrathecal ondansetron administrat

217 The 5-HT(2A) serotonin receptor is the most abundant serotonin recept

218 Glycosylation of other serotonin receptors is essential for expression, ligand

219 Our findings identify cis-UCA as a serotonin receptor ligand and indicate that the immunosu

220 T1AR, and 5-HT6R as potent dual 5-HT7/5-HT2A serotonin receptors ligands.

221 en little examination of the influences that serotonin receptors may play in modulating feeding withi

222 to play an important role in cognition, and serotonin receptors may provide a novel target for futur

223 gamma-aminobutyric acid, acetylcholine, and serotonin receptors, may also be erroneously modeled, an

224 c manipulation and western blot detection of serotonin receptors, measurements of serotonin, high-spe

225 es in behavior, although it is unclear which serotonin receptors mediate this effect.

226 TGF-beta1 expression and activity because of serotonin receptor-mediated signal transduction with act

227 GPCRs, including histamine receptors, 5-HT (serotonin) receptors, muscarinic acetylcholine receptor,

228 ght to elicit their psychotropic actions via serotonin receptors of the 5-hydroxytryptamine 2A subtyp

229 previously that pharmacologic activation of serotonin receptors on motor neurons increases motor neu

230 Serotonin receptors on phrenic motoneuron dendrites may

231 lected genetic polymorphisms of dopamine and serotonin receptors or transporters were linked with agg

232 stablish their relationships to other insect serotonin receptors, other insect amine receptors and th

233 d class II genes), responses to stimuli, and serotonin receptor pathways.

234 The 5-HT(3) serotonin receptor plays an important role in regulating

235 to dissect the specific function of distinct serotonin receptor populations across the life course, w

236 screen yielded agonists of G protein-coupled serotonin receptors, protein kinase C agonists, and a mi

237 flexibility, the contributions of particular serotonin receptors remain unclear.

238 5-HT(2A) serotonin receptors represent the principal molecular ta

239 Activation of 5-HT(2A) serotonin receptors represents a novel approach to lower

240 vo many of the key molecular sites-including serotonin receptors, reuptake transporters, and enzymes-

241 gand-independent, constitutively active 5HT4 serotonin receptor (Rs1) to address how the massive incr

242 olecular chaperones through the metabotropic serotonin receptor SER-1.

243 ion channel MOD-1 and the G-protein-coupled serotonin receptor SER-4.

244 biosynthetic enzyme TPH-1 in neurons and the serotonin receptor SER-7 in the intestine.

245 r and cellular target of citalopram, and the serotonin receptors SER-1 and SER-4 were strong genetic

246 ying behavior required the G protein-coupled serotonin receptors SER-1 and SER-7, and the G(q) orthol

247 of these aminergic receptors, including two serotonin receptors (ser-1 and ser-4), one tyramine rece

248 We found that non-endogenous agonists of the serotonin receptor share a particular IET spectral aspec

249 These data suggest that serotonin receptor signaling influences cellular activit

250 he antiviral properties of 5-NT suggest that serotonin receptor signaling is an important regulator o

251 ions of serotonin have been assigned through serotonin-receptor-specific drugs and mutants; however,

252 This cellular segregation indicates a serotonin-receptor-specific segmentation of the GABAergi

253 Blockers of serotonin receptors, specifically the 5-HT(2A) receptor,

254 nscriptional repression includes the 5-Htr2a serotonin receptor, strongly associated with anxiety- an

255 The serotonin receptor subtype 5-HT(1A) was one of the first

256 y was used to advance the novel concept that serotonin receptor subtype 5-HT2C contributes critically

257 nputs from the basolateral nucleus (BLA) and serotonin receptor subtype 5-HT2CR in the BLA, but not C

258 t serotonin 2A is the predominant excitatory serotonin receptor subtype at hypoglossal motor neurons.

259 ferentially high affinities for a particular serotonin receptor subtype capable of stimulating mitoge

260 (2A) serotonin receptor is the most abundant serotonin receptor subtype in the cortex and is predomin

261 ty, little is known of the influence of this serotonin receptor subtype on prefrontal function.

262 may involve an upregulation of a non-5-HT(2) serotonin receptor subtype or subtypes.

263 ength, accomplished by activating a specific serotonin receptor subtype.

264 which activates cardiac afferents through a serotonin receptor (subtype 3,5-HT3 receptor) mechanism,

265 tered expression of each of three Drosophila serotonin receptor subtypes (d5-HT1A, d5-HT1B, and d5-HT

266 The serotonin receptor subtypes 2 comprise 5-HT2A, 5-HT2B, a

267 The effects of antagonists selective for serotonin receptor subtypes 2A, 2C, or 7 on intrinsic hy

268 ols) were screened for activity at 11 cloned serotonin receptor subtypes by use of ligand-binding met

269 The presence of many serotonin receptor subtypes enables selective drugs to b

270 The functional significance of serotonin receptor subtypes implicated in excitation of

271 This characterization of serotonin receptor subtypes in the hypoglossal nucleus p

272 ceptor subtype 5-HT(1A) was one of the first serotonin receptor subtypes pharmacologically characteri

273 Sstr3 and Htr6 are the only somatostatin and serotonin receptor subtypes that localize to cilia, we h

274 ly characterize in SAVIC cultures the native serotonin receptor subtypes using specific agonists and

275 to suggest that the activation of different serotonin receptor subtypes within the feeding circuitry

276 We compared the expression of two serotonin receptor subtypes, the G-protein-coupled 5-hyd

277 None of the other 11 isoforms of serotonin receptor supported JCPyV infection.

278 e behavioral hypersensitivity with selective serotonin receptor targeting.

279 ine2A (5-HT2A) receptor is a G(q/11)-coupled serotonin receptor that activates phospholipase C and in

280 amine receptor, and LGC-40 is a low-affinity serotonin receptor that is also gated by choline and ace

281 Salvinorin A had no actions at the 5-HT(2A) serotonin receptor, the principal molecular target respo

282 ptor (5-HT(6)R) represent the most promising serotonin receptor therapeutic targets.

283 suggest that EGL-30 may directly couple to a serotonin receptor to mediate egg laying.

284 ty of the lamprey 5-hydroxytryptamine1b-type serotonin receptor to reduce excitatory postsynaptic cur

285 additional proteins that appear to act with serotonin receptors to mediate serotonin response.

286 er in the viral vector could be regulated by serotonin receptor type 1 (5-HT(1)) agonists.

287 Oral administration of the serotonin receptor type 1A agonist buspirone prior to le

288 ts also support the development of selective serotonin receptor type 1A agonists for use as antidyski

289 entified as an endogenous binding partner of serotonin receptor type 2c (5HT2c).

290 t controlled by 5-HT(2)Rs must involve other serotonin receptor types and/or secondary signaling even

291 To this end we cloned all four known insect serotonin receptor types from Manduca (the Ms5HTRs).

292 lution room-temperature structure of a human serotonin receptor using sub-10-micrometer microcrystals

293 on of 100 graphics models of the human 5-HT6 serotonin receptor was constructed based on the structur

294 BTs to known antagonists of the dopamine and serotonin receptors, we explored the roles of two of the

295 pamine, tyrosine hydroxylase, and the 5-HT5A serotonin receptor were increased in the cerebral cortex

296 In brain parenchyma, serotonin receptors were expressed on oligodendrocytes a

297 Here we show that preassociation of 5-HT(7) serotonin receptors with G(s) heterotrimers is necessary

298 RETATION: Our findings suggest activation of serotonin receptors with lorcaserin may provide the firs

299 tory macrophages differ in the expression of serotonin receptors, with 5-HT(2B) and 5-HT(7) expressio

300 alpha1 noradrenergic (alpha1 NE), and 5-HT2 serotonin receptors within the pre-Botzinger complex (pr