ライフサイエンスコーパス: receptor for

1 80(+)/CD11b(low) macrophages as the relevant receptor for 16:4(n-3).

2 ntrol of osteocalcin (BGLAP) gene and is the receptor for 1alpha,25-dihydroxyvitamin D3 (1,25D3).

3 of a subset of substrates and the ABBA motif receptor for a single substrate in our system.

4 or alpha-like (GFRAL), a distant relative of receptors for a distinct class of the TGF-beta superfami

5 itable crown ethers have been synthesized as receptors for a fullerene-ammonium salt derivative (1).

6 This diversity of receptors for a single microbial product underscores the

7 ss-linked micelles, we prepared nanoparticle receptors for a wide variety of mono- and oligosaccharid

8 of cellular prion protein as a high-affinity receptor for Abeta oligomers, and the downstream signali

9 ing domains of the paradigm neurotransmitter receptor for acetylcholine (AChR) display a series of ch

10 dies validating multitargeting of prostanoid receptors for achieving superior anti-inflammatory effec

11 n the human small ribosomal subunit protein, receptor for activated C kinase (RACK1), that are not ph

12 ivity-modifying protein 2 (RAMP2) comprise a receptor for adrenomedullin (AM).

13 The receptor for advanced glycan end products (RAGE) has bee

14 Key players are alpha-dicarbonyls and the receptor for advanced glycation end products (AGER).

15 Cs by transporting extracellular DNA through receptor for advanced glycation end products (RAGE) and

16 mulation and activation of monocytes through receptor for advanced glycation end products (RAGE) and

17 Here, we investigated the role of the receptor for advanced glycation end products (RAGE) in n

18 The receptor for advanced glycation end products (RAGE) is a

19 The receptor for advanced glycation end products (RAGE) is a

20 The receptor for advanced glycation end products (RAGE) is a

21 The receptor for advanced glycation end products (RAGE) is h

22 s with robust and persistent upregulation of receptor for advanced glycation end products (RAGE) mess

23 proteins A8/A9 (S100A8/A9) interact with the receptor for advanced glycation end products (RAGE) on h

24 rotein A8/A9 (S100A8/A9), which binds to the receptor for advanced glycation end products (RAGE) on K

25 r inhibit formation of AGEs and suppress the receptor for advanced glycation end products (RAGE) via

26 es, including toll-like receptor (TLR)2, the receptor for advanced glycation end products (RAGE), mye

27 e expression of toll-like receptor 4 (TLR4), receptor for advanced glycation end products (RAGE), p-E

28 roinflammatory activity by mainly binding to receptor for advanced glycation end products (RAGE).

29 plasma biomarkers of lung epithelial injury (receptor for advanced glycation end products and surfact

30 Receptor for advanced glycation end products is targeted

31 x metalloproteinase cleavage product soluble receptor for advanced glycation end products were signif

32 HMGB1 and its receptors TLR4/MD-2 and RAGE (receptor for advanced glycation end products) are not in

33 no significant differences were observed in receptor for advanced glycation end products, surfactant

34 eseen function of the nuclear isoform of the Receptor for Advanced Glycation End-products (nRAGE) in

35 The receptor for advanced glycation end-products (RAGE) is a

36 (HMGB1) is a major alarmin that binds to the receptor for advanced glycation end-products (RAGE).

37 er time in cytokines and soluble form of the receptor for advanced glycation end-products levels in t

38 levels of cytokines and soluble form of the receptor for advanced glycation end-products, and safety

39 triuretic peptide (beta=-0.250; P<0.001) and receptor for advanced glycation endproducts (beta=-0.095

40 l virus (RSV) infection and mutations in the receptor for advanced glycation endproducts (RAGE) are r

41 The receptor for advanced glycation endproducts (RAGE) binds

42 The receptor for advanced glycation endproducts (RAGE) is a

43 The receptor for advanced glycation endproducts (RAGE) is an

44 ichment in the advanced glycation endproduct/receptor for advanced glycation endproducts (RAGE) pathw

45 plasma concentrations of epithelial (soluble receptor for advanced glycation endproducts [sRAGE]) and

46 Moreover, HMGB1 induced expression of receptor for advanced glycation products (RAGE), but not

47 However, in Receptors for Advanced Glycation End Products (RAGE) kno

48 tress-advanced glycation end products (AGEs) receptor for AGEs (RAGE) pathway, and (3) enalapril (whi

49 tem cells (hBD-MSCs) with or without soluble receptor for AGEs (sRAGE).

50 8-isoprostane, leptin, circulating AGEs and receptor for AGEs were reduced after consumption of low

51 s of PD-1 are as high as those of the T cell receptor for agonist pMHC and of LFA-1 (lymphocyte funct

52 The results confirm that CD163 is the likely receptor for all PRRS viruses.

53 ow that plexin-B2 (PLXNB2) is the functional receptor for ANG in endothelial, cancer, neuronal, and n

54 Inhibitors of the B-cell receptor for antigen signaling and antibodies against ty

55 d activation of B cells through their B-cell receptor for antigen, as seen in B cells lacking Lyn kin

56 dings warrant future studies to identify the receptor for ApoA-IV and the downstream targets of PI3K-

57 alis, and PGN_0294 and PGN_0806 may serve as receptors for ArcA.

58 Local endocytic events involving receptors for axon guidance cues play a central role in

59 njugated beads to biochemically isolate host receptors for bacterial cdNs, and we identified the oxid

60 signaling of tropomyosin-related kinase B, a receptor for BDNF, can improve neurological function aft

61 In contrast to deletion of TrkB, the cognate receptor for BDNF, deletion of Bdnf from cerebellar cell

62 es HCV infection by serving as an attachment receptor for binding to PS exposed on the HCV envelope.

63 1) is an endothelial serine-threonine kinase receptor for bone morphogenetic proteins (BMPs) 9 and 10

64 Here, we identify ICAM-1 as an essential receptor for both AHC-causing and non-AHC strains.

65 ponectin and leptin receptors confirmed that receptors for both are expressed in the SFO, that discre

66 node comprising a prototypical transmembrane receptor for c-di-GMP, LapD, and a cognate periplasmic p

67 Activating mutations in the receptor for C-type natriuretic peptide (CNP), guanylyl

68 tic cell clearance and show that Megf10 is a receptor for C1q, an eat-me signal, that binds phosphati

69 ost cells and that integrin is an additional receptor for C3 besides vimentin.

70 ng these functions on demand yields tailored receptors for cations, anions, or zwitterions in organic

71 emokine receptor 9 (CCR9), which is a unique receptor for CC chemokine ligand (CCL25), is mainly expr

72 Mouse eosinophils expressed CCR7, the receptor for CCL19, and responded chemotactically to CCL

73 In this study, we show that CCR5, the receptor for CCL3 and CCL4, can be transiently upregulat

74 he B cell receptor signaling pathway and the receptors for CD40L, BAFF and TLR ligands.

75 Dipeptidyl peptidase 4 (DPP4) is the receptor for cell binding and entry.

76 viduals in eusocial insects, but the sensory receptors for CHCs are unclear.

77 pendent on the presence of the Duffy antigen/receptor for chemokines (DARC) for both parasite lines,

78 The Duffy antigen receptor for chemokines (DARC) is an atypical receptor t

79 genetic loci (e.g. the African Duffy antigen receptor for chemokines null variant for neutrophil coun

80 in (DBP), which utilizes DARC (Duffy antigen receptor for chemokines) as an entry point.

81 age, sex, and genotype for the Duffy antigen/receptor for chemokines, showed a >40% decrease in the p

82 eptors (class A/1 rhodopsin-like), including receptors for chemokines, PGs, histamine, platelet activ

83 Plexin A4 (PLXNA4) as a novel, high-affinity receptor for CLU in the adult brain.

84 to Alzheimer disease (AD) pathogenesis, the receptor for CLU within the adult brain is currently unk

85 enger receptor class A member I (SR-AI) as a receptor for coagulation factor X (FX), mediating the fo

86 hough APN1 has been implicated as one of the receptors for Cry1Ac in several species, its potential r

87 ghly expressed CXCR4 and CCR3, the chemokine receptors for CXCL12 and CCL11, respectively.

88 wth of tumors positive for CXCR3, a critical receptor for CXCL4 ligands.

89 f the heparan sulfate proteoglycans that are receptors for dengue virus during infection of Vero cell

90 endent manner, further supporting CKAP4 as a receptor for DKK1.

91 factor (MFF), a mitochondrial outer-membrane receptor for DRP1, the cytoplasmic guanosine triphosphat

92 ons express kappa opiate receptors, the main receptor for dynorphin.

93 ing of the C-loop of NPC1, the endolysosomal receptor for EBOV.

94 entified Haemophilus lipoprotein e (P4) as a receptor for ECM proteins.

95 lets, suggesting that P-selectin is the main receptor for Efb on the surface of activated platelets.

96 ycan in optimizing the interface with the Fc receptor for efficient binding.

97 ver, our new data suggest that EGFR is a key receptor for efficient viral entry and that the ensuing

98 ound that OSMR functioned as an essential co-receptor for EGFRvIII.

99 eptor accessory protein (IL-1RAcP) is the co-receptor for eight receptor-cytokine pairs, including th

100 ian enzymes, but a bacterial haem-containing receptor for endogenous enzymatically generated NO(*) ha

101 y use both nectin-1 and nectin-2 as cellular receptors for entry into human cells, but unlike HSV-1 a

102 loviridae family of viruses, utilizes PtdSer receptors for entry into target cells.

103 Integrin alpha3beta1, a major receptor for epidermal adhesion to laminin-332, is criti

104 Rab proteins Sec4 and Ypt11, receptors for essential transport of secretory vesicles

105 Since GBM express ERbeta, a second receptor for estrogen, targeting ERbeta with a selective

106 sulfates on target cell surfaces can act as receptors for exosome uptake, but the ligand for heparan

107 ant, confirming that YehU is a high-affinity receptor for extracellular pyruvate.

108 are known to express several subtypes of P2 receptors for extracellular nucleotides, their function

109 id-sensing ion channels (ASICs) are neuronal receptors for extracellular protons.

110 atalase genes (katG, katE), genes coding for receptors for Fe(2+) (feoB) and at least one of the gene

111 rface proteoglycan glypican-1 to act as a co-receptor for FGF2.

112 mbrane or soluble protein, functions as a co-receptor for Fibroblast Growth Factor (FGF) 23, a known

113 ibronectin, and on target cells it acts as a receptor for fibronectin.

114 member I (SR-AI) to be a macrophage-specific receptor for FX.

115 A receptors (GABAARs), the main postsynaptic receptors for GABA, have been recently demonstrated to a

116 tion and higher-order oligomerization of the receptor for gammaTuRC.

117 emain poorly understood, because the cognate receptor for GDF15 is unknown.

118 gether, our data demonstrate that GFRAL is a receptor for GDF15 that mediates the metabolic effects o

119 By isolating GFRAL as the receptor for GDF15-induced anorexia and weight loss, we

120 of the GFR-alpha family, is a high-affinity receptor for GDF15.

121 odel whereby ShcD competes with neurotrophic receptors for Grb2 binding and opposes activation of the

122 alpha-like (GFRAL) as a brainstem-restricted receptor for growth and differentiation factor 15 (GDF15

123 - by acting as a co-receptor or alternative receptor for growth factors and other signaling peptides

124 le agonists of the cognate G-protein coupled receptor for H2-RLX (relaxin family peptide receptor-1 (

125 A receptors (CD44, Toll-like receptor-4, and receptor for HA-mediated motility) and HA synthases 1 to

126 cipitated with ALK3, an essential type-I BMP receptor for hepatic hepcidin expression.

127 lar transporter for bile acids (BAs) and the receptor for hepatitis B and D viruses.

128 ncoprotein tyrosine kinase MET, which is the receptor for hepatocyte growth factor (HGF), has been im

129 receptor tyrosine kinases could be MET, the receptor for hepatocyte growth factor (HGF).

130 SR-BI is the main receptor for high density lipoproteins (HDL) and mediate

131 Scavenger receptor BI (SR-BI) is the major receptor for high-density lipoprotein (HDL) cholesterol

132 CCR5 is the major co-receptor for HIV and polymorphisms in the CCR5 gene as w

133 lovirus glycoprotein gp68 functions as an Fc receptor for host IgGs and can form antibody bipolar bri

134 ted the capacity to utilize alternative cell receptors for host binding.

135 on, identifying CEACAMs as bona fide protein receptors for Hp.

136 e HVEM was first identified as a viral entry receptor for HSV, it is only recently that HVEM has emer

137 Nectin-1 and HVEM are the two major cellular receptors for HSV.

138 f mice with lineage-specific deletion of the receptor for IFN-lambda, Ifnlr1 We found that expression

139 Aggregation of the high-affinity receptor for IgE (FcepsilonRI) in mast cells initiates a

140 The high-affinity receptor for IgE expressed on the surface of mast cells

141 geting CD23 (FcepsilonRII), the low-affinity receptor for IgE on B cells.

142 sing evidence suggests that the low-affinity receptor for IgE, CD23, plays an important role in contr

143 opic dermatitis (AD) carry the high-affinity receptor for IgE, FcepsilonRI, and are crucially involve

144 The low-affinity receptor for IgE, FcepsilonRII (CD23), contributes to al

145 cytosis via the high-affinity FcvarepsilonRI receptor for IgE, followed by Toll-like receptor 9 (TLR9

146 via cross-linking of IgE-bound high-affinity receptors for IgE (FcepsilonRI) underlies type I allergy

147 e polymorphisms (SNPs) for the high affinity receptor for IgG, FcgammaRI.

148 naling complexes, with IL-12Rbeta2 as second receptor for IL-12 and IL-23R for IL-23 signal transduct

149 hese anomalies, we hypothesized that another receptor for IL-18 may exist, and that IL18BP is evoluti

150 Mice deficient in the receptor for IL-33 (Il1rl1(-/-)) unexpectedly demonstrat

151 y, we used mice in which the common cytokine receptor for IL-4 and IL-13, namely the IL-4Ralpha/IL-13

152 on in double knockout mice, deficient in the receptors for IL-17 (IL-17RA) and interferon (IFN)-gamma

153 activation and upregulated expression of the receptors for IL-33 and IL-25.

154 ole in mediating signaling downstream of the receptors for IL-4 and IL-13.

155 Eosinophil receptors for IL-5 share a common ss-chain with IL-3 and

156 ophils, mast cells express the high-affinity receptor for immunoglobulin E (IgE) and have been linked

157 mulating data support the targeting of these receptors for improving anti-tumor immune responses.

158 sisted engineering could create superior ABA receptors for improving plant drought resistance.

159 of the human intestine as well as being the receptor for infection by the cholera-toxin bearing CTX

160 DC-SIGN is a major receptor for infection of both monocyte-derived dendriti

161 ave emerged as important pattern recognition receptors for infectious danger.

162 expression of pattern recognition receptors, receptors for inflammatory mediators, transcription fact

163 as elucidated, makes it an appropriate model receptor for investigating the allosteric site.

164 cell-cell signalling and classic siderophore receptors for iron acquisition in P. aeruginosa.

165 Hepatitis C virus (HCV) requires multiple receptors for its attachment to and entry into cells.

166 Here, we show that BLT2, a G protein-coupled receptor for leukotriene B4 and 12(S)-hydroxyheptadecatr

167 Two major G-protein-coupled receptors for leukotriene B4 have been identified: the h

168 ting LRBA selectively facilitates signals by receptors for ligands expressed on the surface of NK tar

169 e first demonstrated that the primary homing receptor for linTT1, p32 (or gC1qR), is expressed on the

170 is also attributed to the lack of functional receptors for LPS and TNF-alpha.

171 recently identified GPR99 as a high-affinity receptor for LTE4 that mediates cutaneous vascular perme

172 GPR15, and inhibits expression of GPR174, a receptor for lysophosphatidylserine, on Treg cells, coll

173 iquitin to regulate the endosomal sorting of receptors for lysosomal degradation.

174 intercellular adhesion molecule 1, a counter-receptor for Mac-1 and alphaDbeta2, did not alter the fu

175 The Csf1r locus encodes the receptor for macrophage colony-stimulating factor, which

176 SLAMF1) is both a microbial sensor and entry receptor for measles virus (MeV).

177 ptophan-rich basic (WRB) proteins, which are receptors for membrane insertion of tail-anchored (TA) p

178 While the cell surface receptor for MERS-CoV has been identified as dipeptidyl

179 ts impact their ability to act as functional receptors for MERS-CoV.

180 humans encode both inhibitory and activating receptors for MHC class I.

181 Here we show that E-selectin is a major receptor for monocyte recruitment to tumor cell-activate

182 nd that Hrr25 phosphorylates the kinetochore receptor for monopolin, Dsn1.

183 Our data demonstrate that the main receptor for morphine predominantly shapes the so-called

184 ane glycoprotein dystroglycan functions as a receptor for multiple extracellular matrix proteins and

185 identified AAV receptor (AAVR) is a key host receptor for multiple serotypes, including the most stud

186 iosynthetic pathways for N-acyl amino acids, receptors for N-acyl amino acids, physiologic actions of

187 Yet targeting this receptor for neuroprotection is challenging due to its b

188 th synapses throughout the brain and express receptors for neurotransmitters that can increase intrac

189 Soluble guanylyl cyclase (sGC) is the receptor for nitric oxide and a highly sought-after ther

190 bers syndecan-3 and syndecan-4 as functional receptors for Nogo-A-Delta20.

191 nal screen to identify NPYR-1 as the cognate receptor for NPY-8, a neuropeptide required for sexual m

192 We characterized the receptors for NTL and TRP of V. destructor (VdNTL-R and

193 rker myeloperoxidase (MPO), and the cytokine receptor for nuclear factor kappa-B ligand (RANKL) were

194 the possibility of a family of complementary receptors for O-GlcNAc in different contexts.

195 e activity of the Oamb gene, which encodes a receptor for octopamine (OA, the invertebrate homologue

196 ed T cell circuit in which a synthetic Notch receptor for one antigen induces the expression of a CAR

197 two conformational classes, depending on the receptor for one of these hydrogen bonds.

198 thod for tailoring spacer length of chimeric receptors for optimal function, and a functional element

199 and suggest how approaches used to identify receptors for other sensory modalities may be adapted fo

200 ein receptor-1 (LOX-1), one of the scavenger receptors for oxidized low-density lipoprotein cholester

201 To identify the endogenous receptor for PGE2-G, we performed a subtractive screenin

202 id DHP modulates mRNA levels of the putative receptor for PGF2alpha (Ptgfr).

203 The receptors for PGs, which have yet to be fully characteri

204 Thus, DCAR is a critical receptor for PIM that functions to promote T cell respon

205 g receptor; gene symbol Clec4b1) is a direct receptor for PIM.

206 promote excitotoxic injury via activation of receptors for platelet-activating factor, a proinflammat

207 ral bacterial proteins are known to serve as receptors for Plg including glyceraldehyde-3-phosphate d

208 se (RPTP) and the only known Drosophila HSPG receptor, for promoting dendritic growth of space-fillin

209 ase function that targets, e.g., the steroid receptors for proteasomal degradation.

210 Utilizing receptor for protein kinase 1 (RACK1) as the regulatory

211 intenance 1 (CRM1), the major nuclear export receptor for proteins.

212 athways by PSMs was independent of the known receptor for PSMs, as shown by experiments with DCs lack

213 show that Importin-11 (Ipo11) is a transport receptor for PTEN that is required to physically separat

214 identified basigin as the second erythrocyte receptor for PvTRAg38, which is resistant to chymotrypsi

215 housefly sodium channel visualized the first receptor for pyrethroids, PyR1, in the II/III domain int

216 OPG is a decoy receptor for RANKL, thereby increasing BMD.

217 eptor 4 (LGR4, also called GPR48) is another receptor for RANKL.

218 d Oamb expression in all follicle cells (the receptor for receiving adrenergic signaling and inducing

219 ction the expression of Dectin-1, a critical receptor for recognition and clearance of P. carinii, wa

220 e identified DH44 receptor 1 as the relevant receptor for rest:activity rhythms and mapped its site o

221 HBGAs) expressed on enterocytes are proposed receptors for rotaviruses and can be measured in saliva.

222 PBAR1 (TGR5 or M-BAR) is a G protein-coupled receptor for secondary bile acids that is highly express

223 bulin M (IgM) can function as a cell-surface receptor for secreted IgM on a variety of cell types.

224 aling and suggest that they can act as decoy receptors for self-antigens that are recognized by membr

225 lso occurs for NK cells that lack inhibitory receptors for self-MHC I, and for all NK cells in MHC I-

226 Plexin-B1, the receptor for semaphorin4D (Sema4D), has been implicated

227 Toll-like receptors (TLRs) are innate immune receptors for sensing microbial molecules and damage-ass

228 d side genes suggest that Beats are neuronal receptors for Sides expressed on peripheral tissues.

229 alogangliosides and lipid rafts are membrane receptors for sKlotho and that the KL1 domain is suffici

230 transcripts for Gal, Penk, and Adcyap1, and receptors for substance P, orexin, serotonin, and ATP.

231 results reveal a role for B7-2 as obligatory receptor for superantigens.

232 ied anthrax toxin receptor 1 (ANTXR1) as the receptor for SVV using genome-wide loss-of-function scre

233 virus and a bacterial toxin, as the cellular receptor for SVV.

234 ains 10 (Megf10) is emerging as an essential receptor for synaptic pruning, clearance of neuronal deb

235 nd was also recently found as a novel homing receptor for T-cells implicated in colitis.

236 hough there are currently no known host cell receptors for TcdA, three cell-surface receptors for Tcd

237 cell receptors for TcdA, three cell-surface receptors for TcdB have been identified: CSPG4, NECTIN3,

238 Since GPR171, a recently deorphanized receptor for the abundant neuropeptide BigLEN, is expres

239 Attempts to identify a host cell receptor for the B-repeat were not successful.

240 R15) as a T-cell chemoattractant/trafficking receptor for the colon.

241 The FcmuR receptor for the crystallizable fragment (Fc) of immunog

242 Cereblon (CRBN), a substrate receptor for the cullin-RING ubiquitin ligase 4 (CRL4) c

243 CD74 is a cell-surface receptor for the cytokine macrophage migration inhibitor

244 identified reticulon 3 (RTN3) as a specific receptor for the degradation of ER tubules.

245 Here, we show that CD44, a major receptor for the glycosaminoglycan ECM component hyaluro

246 Mice lacking the CD44 transmembrane receptor for the glycosaminoglycan hyaluronan (HA) demon

247 The first synthetic small molecule receptor for the hydrosulfide anion, HS(-) , using only

248 indings strongly indicate that A2AR is a key receptor for the hypnotic effects of ethanol, and pretre

249 c nociceptors and functions as the molecular receptor for the itch-inducing chemical beta-alanine.

250 of the glutamate moiety, and affinity of the receptor for the ligand.

251 type II transmembrane ectopeptidase, is the receptor for the Middle Eastern respiratory syndrome cor

252 fically to block the function of ALK4, a key receptor for the MSTN/activin pathway in skeletal muscle

253 Loss of the receptor for the neuropeptide PDF promoted synchrony of

254 3 as the chymotrypsin-sensitive erythrocyte receptor for the P4 region, but the other receptor, bind

255 PqsR acts as the receptor for the Pseudomonas quinolone signal, and it co

256 ve to the widely used BAFF receptor-Fc decoy receptor for the specific depletion of BAFF in mice.

257 he glucocorticoid receptor (GR) is the major receptor for the stress hormone cortisol (corticosterone

258 t serves as an endosome-to-Golgi trafficking receptor for the toxin.

259 The Nxf1 protein is a major nuclear export receptor for the transport of mRNA, and it also is essen

260 ble 14 (Fn14; TNFRSF12A) is the cell surface receptor for the tumor necrosis factor (TNF) family memb

261 ith neuropilin 1 (Nrp1) to form a functional receptor for the vascular guidance molecule semaphorin 3

262 CD163 is the receptor for the virus.

263 inhibits the calcitonin gene-related peptide receptor, for the prevention of episodic migraine.

264 ranslating antigen binding signals to immune receptors for the activation of the AP-1 and NF-kappaB m

265 ns inhibit signaling by serving as substrate receptors for the Cullin5-RING E3 ubiquitin ligase (CRL5

266 Waste water treatment plants (WWTPs) are receptors for the cumulative loading of microplastics (M

267 ing cells equipped with various cell surface receptors for the direct or indirect recognition of path

268 This finding led us to address whether receptors for the ECM, integrins, are key to the develop

269 erentiation and aggregation of acetylcholine receptors for the establishment of neuromuscular junctio

270 r III (FcgammaRIII or CD16) are cell surface receptors for the Fc portion of IgG and important regula

271 GABAB receptors are the G-protein coupled receptors for the main inhibitory neurotransmitter in th

272 at regulate epithelial stem cells as well as receptors for the mammatrophic hormones estrogen and gro

273 Here, we determined the host receptors for the multivalent adhesion molecule (MAM) fr

274 We also discover candidate G-protein-coupled receptors for the perception of trisporic acids, mating

275 hology; thus, the introduction of artificial receptors for the real-time quantification of both the c

276 D44 isoforms that include the v6 exon are co-receptors for the receptor tyrosine kinases MET and Vasc

277 utorial Review we cover the use of molecular receptors for the separation of fullerenes by means of h

278 ns, using inhibitory Drosophila allatostatin receptors, for the enhanced expiratory-related oscillati

279 modulator of gamma-aminobutyric acid (GABAA) receptors, for the treatment of post-partum depression.

280 an alternative approach to modulate the CB1 receptor for therapeutic benefits.

281 diseased tissues display sufficient targeted receptors for therapeutic efficacy.

282 lpha and IL-1beta, and mice deficient in the receptor for these cytokines showed a significant decrea

283 Intriguingly, the receptors for these secreted proteins, low-density lipop

284 tor c-MPL (myeloproliferative leukemia), the receptor for thrombopoietin (TPO), in T cells.

285 parathyroid hormone 2 receptor (PTH2R), the receptor for TIP39, suppressed the expression of extrace

286 on of CyHV-3 ORF12, encoding a soluble decoy receptor for TNF-alpha, delayed the manifestation of beh

287 transmembrane protein that functions as a co-receptor for Toll-like receptors to mediate innate immun

288 This renders SepL a high-affinity receptor for translocator/chaperone pairs, recognizing s

289 high-sensitivity C-reactive protein, soluble receptors for tumor necrosis factor alpha 1 and 2, the p

290 We conclude that TyrR is a receptor for tyramine, and suggest that it serves to cur

291 Rpn13 contains an N-terminal pleckstrin-like receptor for ubiquitin domain that binds ubiquitin and d

292 Probing the receptor for ubiquitination using bioluminescence resona

293 genes coding for ionotropic and metabotropic receptors for various neurotransmitters-glutamate, gamma

294 The major signaling receptor for VEGF, i.e VEGFR2, also appears to be under

295 findings identify MGL as a novel macrophage receptor for VWF that significantly contributes to the c

296 GPR151 is a G-protein coupled receptor for which the endogenous ligand remains unknown

297 an increase in integrin binding for several receptors for which signaling is known to be increased a

298 te the gating of eukaryotic neurotransmitter receptors, for which intermediate states also participat

299 ssion of ROR1, in addition to BCL2 ROR1 is a receptor for Wnt5a, which can promote leukemia-cell prol

300 or-1 and -2 (ROR1/2) are considered distinct receptors for Wnt5a and are implicated in noncanonical W