戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
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,

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top