ライフサイエンスコーパス: G protein-coupled receptor

1 nosine receptor, a pharmaceutically relevant G protein-coupled receptor.

2 BD are mediated through this lipid-activated G protein-coupled receptor.

3 or allosteric binding sites across aminergic G protein-coupled receptor.

4 weak antagonist action specific to the LPA1 G protein-coupled receptor.

5 onale for the design of such compounds for a G protein-coupled receptor.

6 resolvin (RvE) 1, and activation of cognate G protein-coupled receptors.

7 k mechanism through a heteromeric complex of G protein-coupled receptors.

8 lular purinergic signals that signal through G protein-coupled receptors.

9 ed structural motifs recognized by aminergic G protein-coupled receptors.

10 M), where they are activated by cell surface G protein-coupled receptors.

11 l trafficking relies on signals initiated by G-protein coupled receptors.

12 ction pairs between 93 neuropeptides and 133 G-protein coupled receptors.

13 activation of a heterotrimeric G-protein by G-protein coupled receptors.

14 ding of the signalling mechanisms of class B G-protein-coupled receptors.

15 to be a common feature among certain class A G-protein-coupled receptors.

16 tion is mediated by oxytocin and vasopressin G-protein-coupled receptors.

17 Ovarian cancer G protein coupled receptor 1 (OGR1, aka GPR68) is a prot

18 Here, we show that G protein-coupled receptor 132 (Gpr132) functions as a k

19 -linked ocular albinism type 1 are caused by G-protein coupled receptor 143 (GPR143) mutations.

20 (CI): -0.84, -0.45) and of cg19859270 in the G protein-coupled receptor 15 gene (GPR15) (M = -0.21, 9

21 G protein-coupled receptor 30 (GPR30), also called G pro

22 2)-12-hydroxyeicosatetraenoic acid (12-HETE)-G-protein-coupled receptor 31 (GPR31) signaling axis as

23 The G-protein-coupled receptor 39 (GPR39) is a G-protein-cou

24 the R-spondin/leucine-rich repeat-containing G protein-coupled receptor 4 (LGR4) axis in driving aber

25 Leucine-rich repeat-containing G protein-coupled receptor 5 (LGR5) is a bona fide marke

26 ar farnesoid X receptor (FXR) and the Takeda G protein-coupled receptor 5 (TGR5).

27 show that the leucine-rich repeat-containing G-protein-coupled receptor 5 (Lgr5) identifies intestina

28 Leucine-rich repeat containing G-protein-coupled receptor 5 (LGR5), an intestinal stem

29 membrane G-protein-coupled receptor (Takeda G-protein-coupled receptor 5; Tgr5).

30 The leucine-rich G protein-coupled receptor-5 (LGR5) is expressed in adul

31 annabinoid receptor 1 (CB1) is an inhibitory G protein-coupled receptor abundantly expressed in the c

32 However, how these G protein-coupled receptors achieve this balance is poor

33 Proteinase-Activated Receptor-2 (PAR2 ) is a G protein-coupled receptor activated by serine proteinas

34 e G-protein-coupled receptor 39 (GPR39) is a G-protein-coupled receptor activated by Zn(2+).

35 d experimental set-up allows for analysis of G protein-coupled receptor activation in the absence and

36 PAK inhibitors did not interfere with G protein-coupled receptor activation-induced rapid tran

37 Mutations to the adhesion G protein-coupled receptor ADGRG1 (G1; also known as GPR

38 s the major source of the lipid mediator and G protein-coupled receptor agonist sphingosine-1-phospha

39 tional profiles for mammalian biogenic amine G protein-coupled receptor agonists and antagonists, som

40 ion of epithelial or fibroblastic cells with G protein-coupled receptor agonists, including angiotens

41 t the release of digestive enzymes evoked by G-protein-coupled-receptor agonists.

42 Members of the adhesion G protein-coupled receptor (aGPCR) family carry an agoni

43 Adhesion G protein-coupled receptors (aGPCRs) play critical roles

44 Adhesion-type G protein-coupled receptors (aGPCRs), a large molecule f

45 that latrophilin-2 (Lphn2), a cell-adhesion G protein-coupled receptor and presumptive alpha-latroto

46 G protein-coupled receptors and cyclic guanosine monopho

47 C4a against a panel of both known and orphan G protein-coupled receptors and now provide evidence tha

48 up of cell-surface receptors, including many G protein-coupled receptors and receptor tyrosine kinase

49 ve shown that Galpha13 is essential for both G-protein-coupled receptor and receptor tyrosine kinase-

50 Here we analyse the concerted motion of G-protein-coupled receptors and G proteins on the plasma

51 overy and high-throughput drug screening for G-protein-coupled receptors and ion channels.

52 cellular cascades known to integrate 'slow' (G-protein-coupled receptors) and 'fast' (ionotropic rece

53 scale synthesis of a fluorinated analogue of G protein-coupled receptor antagonist (GPR91).

54 Chemokines and their cell surface G protein-coupled receptors are critical for cell migrat

55 of both endogenous and synthetic agonists of G protein-coupled receptors are integral to analysis of

56 G protein-coupled receptors are the most important drug

57 Class B G-protein-coupled receptors are major targets for the tr

58 al photoreceptor rhodopsin (Rho) is a unique G protein-coupled receptor as it utilizes a covalently t

59 approach to interrogate proteins engaged by G-protein-coupled receptors as they dynamically signal a

60 en partial and/or biased agonism in RTKs and G-protein-coupled receptors, as well as new therapeutic

61 formation and an enrichment of a pool of the G protein-coupled receptor at actin-rich cellular protru

62 n/sex hormonebinding globulin-like (PLL) and G protein-coupled receptor autoproteolysis-inducing (GAI

63 gral membrane proteins: the beta2-adrenergic G protein-coupled receptor (beta2AR), the peptide transp

64 ted receptor 1 (TAAR1) is a highly conserved G-protein-coupled receptor bound by endogenous trace ami

65 Despite the general acceptance that G protein-coupled receptors can adopt different ligand-i

66 Gi/o-coupled G protein-coupled receptors can inhibit neurotransmitter

67 suppressing the expression of transmembrane G protein-coupled receptors (class A/1 rhodopsin-like),

68 G protein-coupled receptors constitute the largest trans

69 Biased agonism at G protein-coupled receptors constitutes a promising area

70 B (GABAB) receptors, which are heterodimeric G-protein-coupled receptors constructed from R1a and R2

71 otably including growth factor receptors and G protein-coupled receptors, control myelination.

72 In this study, we identify the G-protein-coupled receptor CXCR2 (recognizing chemokines

73 It is now recognized that similar to most G protein-coupled receptors, D2Rs signal not only throug

74 enylate Synthetase Like (OASL), and Adhesion G Protein Coupled Receptor E5 (ADGRE5).

75 mediator of follicular B-cell migration, the G protein-coupled receptor Epstein-Barr virus-induced ge

76 Beta adrenergic receptors (betaARs) are G-protein-coupled receptors essential for physiological

77 behavioral assays identify Gpr158, an orphan G protein-coupled receptor expressed in neurons of the C

78 Melanocortin-4 receptor (MC4R) is a G-protein-coupled receptor expressed in the brain's hypo

79 4 (also known as TEM5/ADGRA2) is an adhesion G protein-coupled receptor family member that plays a pi

80 cagon receptor, GCGR, belongs to the class B G-protein-coupled receptor family and plays a key role i

81 GPBAR1 (TGR5 or M-BAR) is a G protein-coupled receptor for secondary bile acids that

82 ntify small molecule agonists of the cognate G-protein coupled receptor for H2-RLX (relaxin family pe

83 GPR151 is a G-protein coupled receptor for which the endogenous liga

84 GABAB receptors are the G-protein coupled receptors for the main inhibitory neur

85 Two major G-protein-coupled receptors for leukotriene B4 have been

86 We also discover candidate G-protein-coupled receptors for the perception of trispo

87 Rhodopsin is a G protein-coupled receptor found in the rod outer segmen

88 e provides a new framework for understanding G-protein-coupled receptor function.

89 Here, we report the involvement of the G-protein coupled receptor G2A (GPR132) in oxaliplatin-i

90 cription factor Cubitus interruptus (Ci) and G protein coupled receptor (GPCR) family protein Smoothe

91 ne-1-phosphate (S1p), signalling through the G protein coupled receptor (GPCR) S1pr2, plays a key rol

92 Acute hormone secretion triggered by G protein-coupled receptor (GPCR) activation underlies m

93 The beta1-adrenergic receptor (beta1AR) is a G protein-coupled receptor (GPCR) and the predominant ad

94 nds to produce different effects on the same G protein-coupled receptor (GPCR) has interesting therap

95 The G protein-coupled receptor (GPCR) MRGPRD is selectively

96 G protein-coupled receptor (GPCR) signaling occurs in co

97 The G protein-coupled receptor (GPCR) signaling pathways med

98 photo-transduction cascade is a prototypical G protein-coupled receptor (GPCR) signaling system, in w

99 there has been a revolution in the field of G protein-coupled receptor (GPCR) structural biology.

100 r (SMO) belongs to the Class Frizzled of the G protein-coupled receptor (GPCR) superfamily, constitut

101 ble and adverse drug responses downstream of G protein-coupled receptor (GPCR) targets.

102 This viral gene encodes a cell surface G protein-coupled receptor (GPCR) that binds chemokines,

103 GPR15 is an orphan G protein-coupled receptor (GPCR) that serves for an HIV

104 e C and ERK, suggesting the involvement of a G protein-coupled receptor (GPCR).

105 osing roles in regulating various aspects of G protein-coupled receptors (GPCR) expression and signal

106 This activation involves engagement of G protein-coupled receptors (GPCR) on platelets that pro

107 Characterisation of G protein-coupled receptors (GPCR) relies on the availab

108 hibitors, and most notably by stimulation of G protein-coupled receptors (GPCR).

109 -regulated kinase (ERK) activation following G-protein coupled receptor (GPCR) activation.

110 intense scratching in mice by activating the G-protein coupled receptor (GPCR) MrgprA3; it is not kno

111 that is an agonist for the GLP-1 receptor, a G-protein coupled receptor (GPCR).

112 The endothelial G-protein-coupled receptor (GPCR) Gpr124 has been report

113 mediating this effect via activation of the G-protein-coupled receptor (GPCR) MasR, angiotensin-(1-2

114 A new paradigm of G-protein-coupled receptor (GPCR) signaling at intracell

115 by either chemogenetic activation of ciliary G-protein-coupled receptor (GPCR) signaling or the selec

116 x conformational energy landscape determines G-protein-coupled receptor (GPCR) signalling via intrace

117 ng to the GLP-1 receptor (GLP-1R), a class B G-protein-coupled receptor (GPCR) that signals primarily

118 al photoreceptor rhodopsin is a prototypical G-protein-coupled receptor (GPCR) that stabilizes its in

119 ein receptor 75 (GPR75), currently an orphan G-protein-coupled receptor (GPCR), as a specific target

120 l is activated by a signal downstream of the G-protein-coupled receptor (GPCR)-Gq/11-phospholipase C

121 Traditionally, G-protein-coupled receptors (GPCR) are thought to be loc

122 in receptor (APJ) belongs to family A of the G protein-coupled receptors (GPCRs) and is a potential p

123 multiple reported and novel rhodopsin family G protein-coupled receptors (GPCRs) and the polycystic k

124 G protein-coupled receptors (GPCRs) are central to many

125 G protein-coupled receptors (GPCRs) are considered to fu

126 G protein-coupled receptors (GPCRs) are essential for tr

127 G protein-coupled receptors (GPCRs) are historically the

128 Given the importance of G protein-coupled receptors (GPCRs) as pharmaceutical ta

129 cally involved in the signal transduction of G protein-coupled receptors (GPCRs) at the plasma membra

130 G protein-coupled receptors (GPCRs) belong to a large su

131 Family A G protein-coupled receptors (GPCRs) control diverse biol

132 G protein-coupled receptors (GPCRs) exhibit highly conse

133 Here, we find that when activated G protein-coupled receptors (GPCRs) fail to undergo BBSo

134 ing across cellular membranes, the 826 human G protein-coupled receptors (GPCRs) govern a wide range

135 terplay between signaling and trafficking by G protein-coupled receptors (GPCRs) has focused mainly o

136 G protein-coupled receptors (GPCRs) have evolved a seven

137 ) of GCGR and GLP-1R, two members of class B G protein-coupled receptors (GPCRs) in mammalian cells w

138 Phosphorylation of G protein-coupled receptors (GPCRs) is a key event for c

139 G protein-coupled receptors (GPCRs) mediate diverse sign

140 The superfamily of G protein-coupled receptors (GPCRs) mediates a wide rang

141 G protein-coupled receptors (GPCRs) play an important ro

142 G protein-coupled receptors (GPCRs) play crucial roles i

143 G protein-coupled receptors (GPCRs) regulate many animal

144 Class B G protein-coupled receptors (GPCRs) respond to paracrine

145 A family of G protein-coupled receptors (GPCRs) termed the metabolit

146 Pairing orphan G protein-coupled receptors (GPCRs) with their cognate e

147 G protein-coupled receptors (GPCRs), a superfamily of ce

148 sensitization, endocytosis and signalling of G protein-coupled receptors (GPCRs), and they scaffold a

149 scular signalling components, and especially G protein-coupled receptors (GPCRs), as next-generation

150 le in desensitization and internalization of G protein-coupled receptors (GPCRs), beta-arrestins are

151 ts predominantly from chronic stimulation of G protein-coupled receptors (GPCRs), including adrenergi

152 t this theory may be applied to nonolfactory G protein-coupled receptors (GPCRs), including those ass

153 G protein-coupled receptors (GPCRs), the largest family

154 Like most class B G protein-coupled receptors (GPCRs), there is limited kn

155 amine D2 autoreceptors, which are inhibitory G protein-coupled receptors (GPCRs), to decrease the exc

156 G protein-coupled receptors (GPCRs), which are modulated

157 amined the ciliary enrichment signals of two G protein-coupled receptors (GPCRs)-the somatostatin rec

158 The function of G protein-coupled receptors (GPCRs)-which represent the

159 ral different agonists, many of which act on G protein-coupled receptors (GPCRs).

160 of cell surface proteins in eukaryotes, the G protein-coupled receptors (GPCRs).

161 of a Panx1 variant that can be activated by G protein-coupled receptors (GPCRs).

162 n alternative to the classical mechanism via G protein-coupled receptors (GPCRs).

163 c signaling and conformational complexity of G protein-coupled receptors (GPCRs).

164 y transduces signals from a diverse group of G protein-coupled receptors (GPCRs).

165 e is known whether signaling proteins [e.g., G protein-coupled receptors (GPCRs)] exhibit natural var

166 Studies have implicated G protein-coupled-receptors (GPCRs) in cancer progressio

167 G-protein coupled receptors (GPCRs) are essential for is

168 While several G-protein coupled receptors (GPCRs) influence synaptic t

169 Binding of agonists to G-protein-coupled receptors (GPCRs) activates heterotrim

170 S1P can bind to several G-protein-coupled receptors (GPCRs) activating a number

171 mbers of the secretin-like class B family of G-protein-coupled receptors (GPCRs) and have opposing ph

172 Conformational equilibria of G-protein-coupled receptors (GPCRs) are intimately invol

173 Although individual G-protein-coupled receptors (GPCRs) are known to activat

174 G-protein-coupled receptors (GPCRs) are the largest and

175 Although 108 G-protein-coupled receptors (GPCRs) are the targets of 4

176 The phosphorylation of agonist-occupied G-protein-coupled receptors (GPCRs) by GPCR kinases (GRK

177 Resetting of G-protein-coupled receptors (GPCRs) from their active st

178 ne A2 (TxA2) and ADP, which are agonists for G-protein-coupled receptors (GPCRs) on platelets.

179 G-protein-coupled receptors (GPCRs) play critical roles

180 G-protein-coupled receptors (GPCRs) play critical roles

181 G-protein-coupled receptors (GPCRs) pose challenges for

182 e-activated receptors (PARs) are a family of G-protein-coupled receptors (GPCRs) that are irreversibl

183 The selective coupling of G-protein-coupled receptors (GPCRs) to specific G protei

184 h activation is predominantly carried out by G-protein-coupled receptors (GPCRs), non-receptor guanin

185 ane-domain receptors belonging to class A of G-protein-coupled receptors (GPCRs).

186 different tissues through the activation of G-protein-coupled receptors (GPCRs).

187 surface expression or ligand specificity of G-protein-coupled receptors (GPCRs).

188 robiota for N-acyl amides that interact with G-protein-coupled receptors (GPCRs).

189 Microarray analyses revealed G-protein-coupled receptor (GPR) signaling as a prominen

190 Glucose and other sugars are detected by a G protein-coupled receptor, Gpr1, as well as a pair of t

191 lar cAMP levels, increasing synthesis of the G protein coupled receptor, GPR120, and its recruitment

192 KRAS4B membrane association and identified a G protein-coupled receptor, GPR31.

193 The G-protein coupled receptor GPR55 has been postulated to

194 sets based on the expression of the adhesion G protein-coupled receptor GPR56, and GPR56(+) TEMRA cel

195 The class C G protein-coupled receptor GPRC6A is a putative nutrient

196 w pathway is distinctly parcellated from the G protein-coupled receptor --> Gs --> adenylate cyclase

197 tein pathway mediating cell survival and the G protein-coupled receptor --> Gs --> adenylate cyclase

198 terminal truncation of G1 and other adhesion G protein-coupled receptors has been shown to significan

199 The melanocortin-1 receptor (MC1R), a G-protein-coupled receptor, has a crucial role in human

200 nd a highly cell-type-specific expression of G-protein-coupled receptors, implying that ligand-recept

201 terization of transporters, ion channels, or G-protein-coupled receptors in cotranslationally formed

202 Transcriptional screening for the expression G-protein-coupled receptors in murine dorsal root gangli

203 lation as an additional mechanism of Galphai-G-protein-coupled receptor inactivation.Opioid receptors

204 erspective have been increasingly applied to G protein-coupled receptors including the adenosine rece

205 ar domain was described at several aminergic G protein-coupled receptors, including muscarinic acetyl

206 Allosteric modulators of G protein-coupled receptors, including opioid receptors,

207 RGS9-2 controls the function of several G-protein-coupled receptors, including dopamine receptor

208 at eosinophils (Eos) express numerous orphan G-protein-coupled receptors, including Epstein-Barr viru

209 r tyrosine-based activation motif (ITAM) and G-protein-coupled receptors, increased adhesion and aggr

210 Indeed, Toll-like receptors, G-protein-coupled receptors, integrins, receptor-like ki

211 These G protein-coupled receptor-interacting proteins also fac

212 e type 1 taste receptor member 3 (T1R3) is a G protein-coupled receptor involved in sweet-taste perce

213 Functional selectivity of G-protein-coupled receptors is believed to originate fro

214 R2), a classical chemoattractant receptor of G-protein-coupled receptors, is reported to be involved

215 Knockdown of G protein-coupled receptor kinase (GRK) 2, GRK3, or GRK6

216 tagamma) subunits and their interaction with G protein-coupled receptor kinase 2 (GRK2).

217 ding SNVs found in SCZ subjects in the GIT1 (G protein-coupled receptor kinase interacting ArfGAP 1)

218 chimera in the presence of membrane-anchored G protein-coupled receptor kinase-2.

219 G-protein-coupled receptor kinase 2 (GRK2) is arising as

220 We recently identified a novel role for G-protein-coupled receptor kinase 2 (GRK2) that renders

221 nsitions from inhibiting Raf-1 to inhibiting G-protein-coupled receptor kinase 2 upon phosphorylation

222 we find that CCR7 signal termination by the G-protein-coupled receptor kinase 6 (GRK6) is crucial fo

223 protein kinase A site serine 261/262 and the G-protein-coupled receptor kinase site serine 355/356 an

224 helial cells (SECs) via its interaction with G-protein-coupled receptor kinase-2 (GRK2) that also pos

225 G protein-coupled receptor kinases (GRKs) phosphorylate

226 This process is initiated by G protein-coupled receptor kinases (GRKs), some of which

227 tion, TIN-X supports exploration of data for G-protein coupled receptors, kinases, ion channels, and

228 sphingosine 1-phosphate (S1P) receptor-1, a G protein-coupled receptor known to promote the barrier

229 The G-protein-coupled receptors LGR4, LGR5 and LGR6 are Wnt

230 er, was predicted to target the SC-expressed G protein-coupled receptor LGR5.

231 These data establish (R)-PZQ as a G-protein-coupled receptor ligand and suggest that the e

232 effects upon binding and activating CXCR1, a G protein-coupled receptor, located in the cell membrane

233 (LPA) in decidualization, acting through its G-protein-coupled receptor LPA3 in the uterine epitheliu

234 peptide ligands from platelet GP1balpha and G-protein-coupled receptor MAS effectively bound Ig21 by

235 thosteric and allosteric topography within a G protein-coupled receptor, may represent a novel approa

236 G protein-coupled receptors mediate their complex functi

237 G-protein-coupled receptors mediate the biological effec

238 internal calcium in astrocytes, focusing on G protein-coupled receptor-mediated mobilization of calc

239 We used a retinal G protein-coupled receptor, mGluR2, which we chemically

240 Members of the Mas-related G protein-coupled receptor (Mrgpr) family demarcate an i

241 idence that SP functions through Mas-related G protein-coupled receptors (Mrgprs) in addition to its

242 ction via protease-activated and mas-related G-protein-coupled receptors (Mrgprs) to contribute to al

243 C-1, a beta-barrel membrane protein, and the G-protein-coupled receptor NTR1, an alpha-helical membra

244 ry proposes that the activation of olfactory G protein-coupled receptors occurs by an inelastic elect

245 he nanobody Nb37 suggests that signalling by G-protein-coupled receptors occurs preferentially at the

246 B (CTSB), which can be induced directly via G protein-coupled receptors on acinar cells or through i

247 -protein complex that is being released from G-protein-coupled receptors on vagal stimulation.

248 The focus is on the immunohistochemistry of G-protein-coupled receptors, one of the largest families

249 The G protein-coupled receptor opsin is a phospholipid scram

250 or the V2R without any activity on 155 other G-protein-coupled receptors or on 15 ionic channels.

251 First, a localized signal is generated by a G protein-coupled receptor paired to one or more of the

252 versely showed upregulation of GO terms like G-protein coupled receptor pathway, membrane potential a

253 in mammals and discovered that Hedgehog and G-protein-coupled receptor pathways were linked to cilia

254 Smoothened (SMO) is a G-protein-coupled receptor-related protein required for

255 Many G protein-coupled receptors require association with oth

256 naling molecule that interacts with its five G-protein coupled receptors (S1P1-5) to regulate cell gr

257 nificant alterations in signal transduction, G protein coupled receptors, serotonin and glycosaminogl

258 tion of synaptic transmission by presynaptic G-protein coupled receptors shapes information flow thro

259 R7-RGS-binding protein (R7BP) that regulate G protein-coupled receptor signaling by accelerating dea

260 , representing a novel mode of regulation of G protein-coupled receptor signaling by scaffolding prot

261 We propose that this bifurcation of the Tre1 G protein-coupled receptor signaling response via G prot

262 phorylation, thereby bridging MAP kinase and G-Protein-Coupled Receptor signaling.

263 Each microvillus employs a full G-protein-coupled receptor signalling pathway to adaptiv

264 ght on the dynamic interactions that control G-protein-coupled receptor signalling.

265 The dopamine D2 receptor (D2R), like many G-protein-coupled receptors, signals through G-protein-

266 identified the gene dmsr-1, which encodes a G-protein coupled receptor similar to an insect RFamide

267 initiates signaling upstream of PI3K through G protein-coupled receptors, specifically via the metabo

268 pha-pheromone was independent of the cognate G protein-coupled receptors Ste2 and of the central beta

269 G protein-coupled receptor stimulation inhibits TRPM3 ch

270 lear farnesoid X receptor (Fxr) and membrane G-protein-coupled receptor (Takeda G-protein-coupled rec

271 Furthermore, one of the proton-sensing G-protein-coupled receptors, TDAG8, was highly ( approxi

272 armaceutical drug targets, the corresponding G-protein-coupled receptors (termed aminergic GPCRs) bel

273 receptor farnesoid X receptor (FXR) and the G protein-coupled receptor TGR5.

274 al biased signaling via isoforms of the same G protein-coupled receptor that are simultaneously expre

275 id receptor (MOPr) is a clinically important G protein-coupled receptor that couples to Gi/o proteins

276 The dopamine D2 receptor (D2R) is a G protein-coupled receptor that is a common target for a

277 cro opioid receptor (microR), a prototypical G-protein-coupled receptor that is a physiologically rel

278 nding sites on the A2A adenosine receptor, a G-protein-coupled receptor that is a target for the trea

279 one secretagogue receptor 1a (GHS-R1a), is a G-protein-coupled receptor that is differentially expres

280 ce lacking GPR88, a striatum-enriched orphan G-protein-coupled receptor that modulates striatal mediu

281 GABAB receptors are G-protein-coupled receptors that mediate inhibitory syna

282 act that S1PRs are pertussis toxin-sensitive G protein-coupled receptors, the effects of AAL-R were p

283 Finally, activation of a G-protein-coupled receptor, the muscarinic M5R, results

284 everal aspects of metabolism by activating 4 G-protein-coupled receptors, the A1, A2A, A2B, and A3 ad

285 onformational-sensitive antibodies targeting G-protein coupled receptors to screen for novel pharmaco

286 porters, potassium and calcium channels, and G-protein-coupled receptors to modulate exocytosis.

287 A novel G-protein coupled receptor, trace amine-associated recep

288 screened 29 proteins with known functions in G protein-coupled receptor trafficking for their role in

289 In Drosophila melanogaster, a single G protein-coupled receptor, Trapped in endoderm 1 (Tre1)

290 al immune modulatory proteins, including the G protein-coupled receptor US28, which scavenges human c

291 ified the 5q14 locus, harboring the adhesion G protein-coupled receptor V1 (ADGRV1) gene, which showe

292 In the absence of adhesion G protein-coupled receptor V1 (adgrv1), another hair bun

293 0(-)(8)) in an intron of the adhesion GPR98 (G-protein-coupled receptor V1) gene on chromosome 5q14.3

294 Internalization of transferrin and these G protein-coupled receptors was also inhibited in cells

295 Three representative MPs, including one G-protein-coupled receptor, were successfully incorporat

296 osomal and melanosomal membranes unlike most G protein-coupled receptors, which localize to the plasm

297 The nociceptin (NOP) receptor is a G-protein-coupled receptor whose natural ligand is the N

298 e epitopes are known, human beta2 adrenergic G-protein-coupled receptor, with promising results.

299 ), which activate mast cells via Mas-related G protein-coupled receptor X2 (MRGPRX2), is increased in

300 IgE)-independent pathways [e.g., Mas-related G protein-coupled receptor X2 (MRGPRX2)], tetraspanins,