ライフサイエンスコーパス: receptor for

1 down of GPR31, a purported G-protein-coupled receptor for 12-HETE, largely phenocopies both the deple

2 A potential homolog of the human receptor for 12-S-HETE, gpr31, is expressed on GSCs and

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

4 An ARF GEF known as General receptor for 3-phosphoinositides 1 (Grp1) is recruited t

5 r signaling mechanism whereby a cell-surface receptor for a chemorepellent confers specificity of int

6 Molecularly imprinted polymers are synthetic receptors for a targeted molecule.

7 ace-anchored glycoproteins functioning as co-receptors for a variety of growth factors.

8 The receptor for AAV (AAVR; also named KIAA0319L) was recent

9 ANCL2) has been characterized as the natural receptor for ABA.

10 hey were found to be efficient and selective receptors for acetylcholine over choline.

11 wide expression patterns of all metabotropic receptors for acetylcholine, GABA, and glutamate, comple

12 dy, we identified and characterized a RACK1 (Receptor for Activated C Kinase 1) homolog FvGbb2 as a p

13 res not only its cognate ligands but also co-receptors for activation, the mechanisms of which remain

14 high-mobility group box 1 (HMGB1) can engage receptor for advanced glycation end product (RAGE) to di

15 The receptor for advanced glycation end products (RAGE) and

16 Studies have indicated that the receptor for advanced glycation end products (RAGE) is a

17 The receptor for advanced glycation end products (RAGE) play

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

19 Although the innate immune receptor protein, Receptor for Advanced Glycation End products (RAGE), has

20 le high-mobility group box 1 (HMGB1) and its receptor for advanced glycation end products (RAGE).

21 essment of antioxidant potential and soluble-receptor for advanced glycation end products (sRAGE) in

22 EC for biomarkers of inflammatory mediators (receptor for advanced glycation end products [RAGE], MPO

23 egies aimed at targeting the S100A8/A9-RAGE (receptor for advanced glycation end products) axis could

24 Plasma concentrations of sRAGE (soluble receptor for advanced glycation end products) strongly a

25 asma concentration of interleukin-6, soluble receptor for advanced glycation end products, interleuki

26 teinase 9 (MMP9) stimulation, leading to the receptor for advanced glycation end-products (RAGE) shed

27 ICs expressed caveolin-1, podoplanin and receptor for advanced glycation end-products (RAGE), and

28 We examined relations of serum soluble receptor for advanced glycation end-products (sRAGE) wit

29 cribe how ERs (estrogen receptors) and RAGE (receptor for advanced glycation end-products) play a cri

30 The receptor for advanced glycation endproducts (RAGE) has b

31 The receptor for advanced glycation endproducts (RAGE) is cr

32 and experimental studies have found that the receptor for advanced glycation endproducts (RAGE) plays

33 s upon UVR, which subsequently activated the receptor for advanced glycation endproducts (RAGE) recep

34 tor preformed a heteromeric complex with the receptor for advanced glycation endproducts (RAGE).

35 asome stimulation is mediated in part by the receptor for advanced glycation endproducts and Toll-lik

36 l cells through transferrin receptor and the receptor for advanced glycation-end products, cross the

37 In contrast to cDC1, RPM used the mannose receptor for Ag uptake and employed the proteasome- and

38 of mast cells in colon and expression of the receptor for AGER in proximal colon epithelium.

39 E carboxymethyl-lysine (CML) and the soluble receptor for AGEs (sRAGE) in 2439 participants from the

40 protein receptor-related protein 4 (Lrp4), a receptor for Agrin, is expressed in hippocampal NSPCs an

41 s of normal cellular prion protein (PrPc), a receptor for amyloid peptides, and phospho-181T-tau were

42 her the angiotensin-converting enzyme or the receptor for angiotensin II attenuated VEGF-mediated rel

43 py)NHP(mu-N(t)Bu)](2) not only activates the receptor for anion binding (by fixing the optimum exo-ex

44 es are most commonly employed with inorganic receptors for anions: metal extrusion assays, responsive

45 e of its products, T cells bearing alphabeta receptors for antigen.

46 of TRPV4 channels; (3) antagonist of P2Y(1) receptors for ATP; and (4) inhibitors of phospholipase C

47 We propose that maize Rtn1 and Rtn2 act as receptors for autophagy-mediated ER turnover, and thus a

48 Here we show that caspase-11, the cytosolic receptor for bacterial endotoxin (lipopolysaccharide: LP

49 etic data demonstrate that NAIP proteins are receptors for bacterial ligands, while NLRC4 is a downst

50 y physiological functions; they can serve as receptors for bacteriophages, and provide a substrate fo

51 se an increase in the phosphorylation of the receptor for BDNF, TrkB, in the ventral hippocampus (vHi

52 Ig was originally identified as a macrophage receptor for binding complement C3b/iC3b in vitro, recen

53 ogy to interrogate most single transmembrane receptors for binding to 445 IgSF proteins, we identify

54 e feasible use of imprinted PNE as synthetic receptor for biomolecules, opening new perspectives for

55 P) most of them contained mRNA for NPR1, the receptor for BNP.

56 s has been explored, exploiting cell-surface receptors for boosting selectivity has not been attained

57 Gene expression of IL-18R, which is a receptor for both IL-18 and IL-37, is also increased in

58 , EphA2 was identified as an important entry receptor for both KSHV and EBV.

59 ses the same viral glycoprotein and cellular receptor for both T- and B-cell infection.IMPORTANCE Eps

60 cells of complement activation by expressing receptors for C3a and C5a through which their chemoattra

61 o-Aminomethylphenylboronic acids are used in receptors for carbohydrates and various other compounds

62 s, which were the main astrocytic phagocytic receptors for cell debris in the above experiments, indi

63 ceptor family that serves as an essential co-receptor for cellular entry of R5-tropic HIV-1, and is a

64 els trigger release of Ca(2+) from ryanodine receptors for cellular contraction, whereas signaling do

65 us are used for many functions, and serve as receptors for certain archaeal viruses.

66 o our knowledge, this is the first synthetic receptor for cGMP, which also demonstrates a high prefer

67 targeting the binding site for Duffy antigen receptor for chemokines (DARC) and the dimer interface o

68 tein (DBPII) with the erythrocyte's Duffy Ag receptor for chemokines (DARC) is essential.

69 The Duffy antigen receptor for chemokines (DARC) on endothelial cells, rat

70 on targeting the host receptor Duffy antigen receptor for chemokines (DARC).

71 vent PvDBP from binding to the Duffy antigen receptor for chemokines, and their capacity to block red

72 ) with its human receptor, the Duffy antigen receptor for chemokines.

73 a cholesterol-poor ligand that binds to the receptor for cholesterol-rich HDLs, scavenger receptor t

74 lycoprotein VI (GPVI) is a platelet-specific receptor for collagen and fibrin that triggers platelet

75 le for SAA1 as a soluble pattern recognition receptor for conserved FABPs found in common mite allerg

76 L sequence in the receptor and activates the receptor for COPI binding in the cytoplasm.

77 omeostasis by aldosterone and also acts as a receptor for cortisol.

78 yrosine phosphatase sigma (PTPsigma, PTPRS), receptor for CSPGs, interacts with TRKB and restricts TR

79 o-receptors that mediate signaling of kinase receptors for cytokines with crucial roles in zebrafish

80 lity in root and leaf tissues, targeting ABA receptors for degradation in different subcellular locat

81 , which targets inositol 1,4,5-trisphosphate receptors for degradation, are the likely cause of autos

82 inhibits Wnt signaling by ubiquitinating Wnt receptors for degradation.

83 I as the major cytosolic pattern recognition receptor for detection of ZIKV.IMPORTANCE Zika Virus (ZI

84 arins/heparan sulfates and Lewis antigens as receptors for different TcAs from insect and human patho

85 t use human coronavirus ACE-2, DPP4, or CD13 receptors for docking and entry.

86 kinase RNA-activated (PKR) is a cytoplasmic receptor for dsRNA, and as such is involved in detection

87 in (TIM) family proteins act as cell surface receptors for EBOV, and that the interaction between TIM

88 D21 on mature peripheral T cells, i.e., as a receptor for EBV.

89 us 2 (SARS-CoV-2) utilizes human ACE2 as the receptor for entry with subsequent downregulation of ACE

90 spike protein, which engages with host ACE2 receptor for entry.

91 e show that transcription induced by nuclear receptors for estrogen (E(2)) or retinoic acid (RA) is a

92 rofiles for these newly identified glutamate receptors, for example, kainate receptors on which NMDA

93 In contrast to other innate immune receptors, for example, Toll-like receptors (TLRs), that

94 ereby affecting its ability to function as a receptor for extracellular matrix proteins.

95 he airway smooth muscle cells by acting as a receptor for extracellular metallothionein-2.

96 r kinase (LecRK), LecRK-VI.2, is a potential receptor for extracellular NAD(+) (eNAD(+)) and NAD(+) p

97 Further, we uncovered that Fas, the receptor for FasL, is highly expressed on patient-derive

98 be predesigned for viruses with known entry receptors for faster therapeutic response without the ne

99 have demonstrated that NCOA4, the autophagic receptor for ferritin, is necessary for the mobilization

100 ependently of alpha-klotho, the canonical co-receptor for FGF23 in the kidney, which stimulates left

101 Klotho functions as a co-receptor for fibroblast growth factor 23 (FGF23) signali

102 l, to our knowledge, synthetic SA-displaying receptor for functionalization of the force probe.

103 of transcription factors that also includes receptors for glucocorticoids, progesterone, androgens,

104 In particular, a receptor for glucose has achieved performance which gene

105 Here we report a synthetic receptor for glucose, which is biomimetic in both design

106 (receptor for gram-positive bacteria), TLR4 (receptor for gram-negative bacteria), or distilled water

107 to mice and incubated with agonists of TLR2 (receptor for gram-positive bacteria), TLR4 (receptor for

108 or Mrgprb2 and its human homolog MRGPRX2 are receptors for Gram-positive QSMs, including competence-s

109 ity by reducing the expression levels of the receptor for HA-mediated motility, RHAMM, and the HA-bin

110 d a multipass membrane protein, OR14I1, as a receptor for HCMV infection.

111 Inner hair cells (IHCs) are the primary receptors for hearing.

112 Our data reveal that P2X7 is a key receptor for helping to clear sepsis because it maintain

113 mer is employed as a sensitive and selective receptor for hemagglutinin (HA) protein, which is a biom

114 sensing in the context of its activity as a receptor for hepatitis C virus (HCV).

115 Cubilin is the only known receptor for holo-IF and is found primarily in the kidne

116 ANCE SARS-CoV-2 uses human ACE2 as a primary receptor for host cell entry.

117 NK cells bearing inhibitory self-receptors for host MHC I also undergo education, referre

118 mokine receptor type 5 (CCR5) serves as a co-receptor for Human immunodeficiency virus (HIV), enablin

119 -C chemokine receptor Type 5 (CCR5) is a key receptor for human immunodeficiency virus type 1 (HIV-1)

120 family member 3 (CDHR3) protein serves as a receptor for human rhinovirus (HRV)-C.

121 d by their expression of dominant inhibitory receptors for human leukocyte antigen (HLA) class I.

122 intracellular and extracellular protein, the receptor for hyaluronan-mediated motility (RHAMM), coord

123 metry for cells expressing the high-affinity receptor for IgE (FcepsilonRI).

124 governance mechanisms (ie, the high-affinity receptor for IgE [FcepsilonRI]), the stem cell factor re

125 Both express robustly the high-affinity receptor for IgE, FcepsilonRI, and thereby sense allerge

126 CD23/FcepsilonRII, the low-affinity receptor for IgE, is constitutively expressed on B cells

127 cells that express the high-affinity Fcgamma receptor for IgG (FcgammaRI) in both mouse and human pat

128 Here we show that FcgammaRI, an immune receptor for IgG immune complex (IgG-IC), is expressed i

129 e colitis point to a role for FcgammaRIIA, a receptor for IgG.

130 In contrast, antagonism of the common receptor for IL-13 and IL-4 by the biologic dupilumab pr

131 Ralpha, in part, comprises the high affinity receptor for IL-2, a cytokine important in immune prolif

132 Among HSPCs, we found that the receptor for IL-33, ST2, is expressed preferentially and

133 IL-6Ralpha is the only biologically relevant receptor for IL-6 in mice.

134 We identify LIFR as the receptor for ILEI, which mediates signaling through STAT

135 IA by human platelets, which is their unique receptor for immunoglobulin G antibodies, positions them

136 e that HAdV26 uses alphavbeta3 integrin as a receptor for infecting epithelial cells.

137 We identified EphA7 as the principal Eph receptor for infection of BJAB cells by KSHV and the rel

138 Sialic acids (Sia) are the primary receptors for influenza viruses and are widely displayed

139 development of accurate probes and molecular receptors for inorganic phosphate.

140 Pi) homeostasis contain SPX domains that are receptors for inositol pyrophosphates (PP-InsP), suggest

141 ns now challenge this idea and indicate that receptors for inositol trisphosphate (IP(3)) and ryanodi

142 uppression of tumorigenicity 2 (ST2), is the receptor for interleukin 33 (IL-33) and has been increas

143 gamma chain, gamma(c), is a component of the receptors for interleukin-2 (IL-2), IL-4, IL-7, IL-9, IL

144 viously reported that Cubilin, the endocytic receptor for intrinsic factor-vitamin B12, albumin and a

145 ach siderophore type relying on a compatible receptor for iron uptake(8-12), our results suggest that

146 Some bacteria also express outer membrane receptors for iron-binding proteins of the host and extr

147 her exploited the high binding affinity of a receptor for its corresponding biomarker or a specific m

148 ic transmission that does not depend on NMDA receptors for its induction but, instead, requires Ca(2+

149 he guinea pig TfR1 (gpTfR1) is the principal receptor for JUNV, while hamster and mouse orthologs fai

150 tor tyrosine kinase A2 (EphA2) is a cellular receptor for KSHV and EBV.

151 The discovery of a G-protein-coupled receptor for lactate named hydroxycarboxylic acid recept

152 GPR81 is a G-protein-coupled receptor for lactate, which is upregulated in breast can

153 lpha6beta4 is an essential, dynamic adhesion receptor for laminin 332 found on epithelial cells, requ

154 asses of proteins have been identified as Bt receptors for lepidopteran insects, identification of re

155 Receptors for leukotriene B(4) (LTB(4)), prostaglandin E

156 find that mouse pDCs selectively express the receptor for LIF that signals through STAT3.

157 1 increases fibroblast expression of HVEM, a receptor for LIGHT.

158 lled HVEM) and lymphotoxin beta receptor are receptors for LIGHT that were expressed by fibroblasts f

159 TREM2 is a receptor for lipids expressed in microglia.

160 of murine Fpr2/3, an ortholog of human FPR2/receptor for lipoxin A4 (ALX), in orchestrating intestin

161 reen, we identified ALK-1 as a high-capacity receptor for low-density lipoprotein (LDL) in endothelia

162 hese results identify SIRPalpha as a counter-receptor for Mac-1 and suggest that the Mac-1-SIRPalpha

163 Within these coats are receptors for macromolecular nutrients such as transferr

164 uclear phagocytes depend on signals from the receptor for macrophage colony-stimulating factor, CSF1R

165 Here we identify an African trypanosome receptor for mammalian factor H, a negative regulator of

166 is, cell-wall polysaccharides (CWPSs) act as receptors for many bacteriophages, and their structural

167 umerous different cellular functions and are receptors for many pathogens.

168 4 (FFA4) is a cell-surface G protein-coupled receptor for medium and long-chained fatty acids that ca

169 the need to engage nectin-4 or CD150, known receptors for MeV that are not present on neural cells.

170 ion is dependent on signaling by CX3CR1, the receptor for microglial fractalkine (also known as CXCL1

171 that different alleles of the proteinaceous receptor for MNV, CD300LF, function in a cell type-depen

172 eport a novel tripodal molecule that acts as receptor for mono- and bis-phosphorylated PIPs in a cell

173 A global knockout of the receptor for monocyte chemoattractant protein (CCR2) pre

174 s leading to the demonstration that specific receptors for morphine-like analgesics exist, the search

175 sion and identify SR-B1 as the airway M cell receptor for Mtb.

176 Mxra8 is a receptor for multiple alphaviruses including chikungunya

177 Mxra8 is a receptor for multiple arthritogenic alphaviruses that ca

178 I, Meg-01 and MO7e express TrkA, the primary receptor for Nerve Growth Factor (NGF) signaling.

179 eceptor kinase A (TrkA) is the high-affinity receptor for nerve growth factor.

180 Nerves were found to express the following receptors for nerve growth factor (NGF): neurotrophic re

181 PrP(C) may also act as a receptor for neurotoxic, oligomeric species of other pro

182 her modulated pharmacologically by targeting receptors for neurotransmitters such as acetylcholine (A

183 Soluble guanylyl cyclase (sGC) is the main receptor for nitric oxide (NO) and a central component o

184 luble guanylate cyclase (sGC) is the primary receptor for nitric oxide (NO) in mammalian nitric oxide

185 cells both require muscarinic and nicotinic receptors for normal excitability, thereby affecting ong

186 ponse of Notch proteolysis to screen surface receptors for other putative proteolytic switches.

187 ermore, it was significantly correlated with receptors for other viruses linked to atherosclerosis.

188 m cell-derived sensory neurons expressed the receptor for PACAP and that this peptide could significa

189 Among mice deficient in receptors for pathogen-associated molecular patterns, My

190 s indicate that gpTfR1 serves as the primary receptor for pathogenic NWAs, enhancing viral infection

191 wth factor receptor alpha (PDGFRA) to be the receptor for PC-independent infection of fibroblast cell

192 integrin (complement receptor 3) is a major receptor for phagocytosis in macrophages.

193 es provide a foundation to develop efficient receptors for phosphate capture.

194 We show here that the receptor for platelet-derived growth factor (PDGF) signa

195 Here, we discovered a receptor for PLY, whereby pro-inflammatory cytokine resp

196 osine phosphatase sigma (PTPsigma, PTPRS), a receptor for PNNs, interacts with TRKB and inhibits its

197 inase substrate (MARCKS) is an intracellular receptor for polysialic acid.

198 nt with a role for CD23 in many species as a receptor for potentially pathogenic microorganisms as we

199 successfully identified genes encoding known receptors for previously characterized viruses of Escher

200 intestinal stem cell (ISC) marker LGR5 is a receptor for R-spondin (RSPO) that functions to potentia

201 monstrate that TLR7 is an innate recognition receptor for RABV, which restricts RABV invasion into th

202 onstrated that TLR7 is an innate recognition receptor for RABV.

203 Osteoprotegerin (OPG), a secreted decoy receptor for receptor activator of nuclear factor B liga

204 receptor (CAR) as a functional proteinaceous receptor for ReCVs.

205 Although five receptors for RGF1 have been identified(2-4), the downst

206 We also found that neogenin, the canonical receptor for RGMb, was expressed by interstitial macroph

207 The Sec61 translocon (SEC61) serves as the receptor for ribosomes that translate secretory/integral

208 proteoglycans (HSPGs) act as alternative co-receptors for RSPO3 using a combination of ligand mutage

209 e mycotoxins, and can be cheaper alternative receptors for sample clean-up due to their wide availabi

210 r findings identify GABA(B)R1a as a synaptic receptor for sAPP and reveal a physiological role for sA

211 giotensin converting enzyme-2 (ACE-2) as the receptor for SARS- CoV-2 (Severe Acute Respiratory Syndr

212 The receptor for SARS-CoV-2 binding, angiotensin-converting

213 ACE2 is identified as an essential receptor for SARS-CoV-2 to enter the cell.

214 ers.Conclusions: ACE2, the gene encoding the receptor for SARS-CoV-2, is expressed in the human airwa

215 g enzyme 2(ACE2) was identified as the entry receptor for SARS-CoV-2.

216 nzyme 2 (ACE2) is the canonical cell surface receptor for SARS-CoV-2.

217 GPBAR1 is a G protein-coupled receptor for secondary bile acids placed at the interfac

218 CP in PB of mouse and human expressed homing receptors for secondary lymphoid organs, mainly CD62L.

219 ynaptic function mediated by an unidentified receptor for secreted APP (sAPP).

220 ring in lymphatic endothelium that tunes the receptor for selective engagement with hyaluronan assemb

221 iculum (ER), and in some cases are autophagy receptors for selective ER turnover.

222 Neuropilins-1/-2 (NRP1, NRP2) are receptors for semaphorins and angiogenic growth factors,

223 Plexins are receptors for semaphorins that transduce signals for reg

224 Megalin is a transmembrane receptor for serum d-binding protein (DBP) in kidney cel

225 We propose that research on the specific receptors for several newly identified members of the Pa

226 ensin-converting enzyme 2 (ACE2) is an entry receptor for severe acute respiratory syndrome coronavir

227 The host receptor for severe acute respiratory syndrome coronavir

228 le of angiotensin converting enzyme 2 as the receptor for severe acute respiratory syndrome coronavir

229 verting enzyme 2 was identified as a primary receptor for severe acute respiratory syndrome coronavir

230 which free fatty acid receptor 2 (FFAR2), a receptor for short-chain fatty acids that can affect the

231 interferon genes (STING) is a key cytosolic receptor for small nucleotides and plays a key role in a

232 olfactory system does not come from specific receptors for specific analytes (e.g., the traditional l

233 ed as being the first intracellular membrane receptor for sPLA(2) by alternative Atx-affinity-labelli

234 strating that the S-layer is not the primary receptor for SSV9 surface binding.

235 and identify semaphorin (SEMA) 6A and 6B as receptors for TcsL.

236 MA6A and 6B as pathophysiologically relevant receptors for TcsL.

237 e reduced folate carrier (RFC) and potential receptor for TG35-2-phenotypic virus.

238 e we demonstrate that Neuropilin 2 (Nrp2), a receptor for the axon guidance cue semaphorin 3F, has im

239 s molecule expressed on Th2 cells (CRTH2), a receptor for the bioactive lipid prostaglandin D(2) (PGD

240 spermatozoa and forms with FGFR1 a specific receptor for the bone-derived hormone FGF23.

241 netic deletion of CR3, a microglia-expressed receptor for the C3 activation product iC3b, implicating

242 mSC subtypes that express both IL-33 and the receptor for the calcitonin-gene-related peptide (CGRP);

243 Given that ACE2, the entry receptor for the causative coronavirus SARS-CoV-2, is ex

244 erved cell adhesion molecule SYG-1/Neph as a receptor for the cleaved extracellular Robo fragment to

245 ILC2s express ST2, the receptor for the cytokine IL-33, and chemoattractant rec

246 , Ede1, which acts as an intrinsic autophagy receptor for the degradation of Ede1-dependent endocytic

247 t BMP-mediated SC growth is dependent on the receptor for the developmental steroid ecdysone, whose c

248 ge both tau and Cereblon (CRBN), a substrate-receptor for the E3-ubiquitin ligase CRL4(CRBN), to trig

249 mbrane protein kinase that may function as a receptor for the egg elicitor and other genes implicated

250 characterized by the expression of Lyve-1, a receptor for the extracellular matrix (ECM) component hy

251 Dectin-1, a receptor for the fungal cell wall carbohydrate beta-1,3-

252 previously implicated Spc72, the cytoplasmic receptor for the gamma-tubulin nucleation complex, as th

253 nt cell types, EphA2 functions as a cellular receptor for the gH/gL glycoprotein complex of KSHV.

254 While the high-affinity receptor for the gH/gL glycoprotein complex, EphA2, has

255 pe express high levels of CD163, a scavenger receptor for the hemoglobin-haptoglobin complex.

256 KREMEN1 (KRM1) is the entry receptor for the largest receptor-group of hand-foot-and

257 Deleted in colorectal cancer (DCC), the receptor for the multifunctional cue netrin-1, acts as a

258 depleted mice express reduced amounts of the receptor for the neuropeptide neuromedin B (NMB).

259 RFC, a folate transporter, is a potential receptor for the novel FeLV variant.

260 (Duffy antigen), the only known erythrocyte receptor for the P. vivax merozoite invasion ligand, Duf

261 issue that is linked to induction of MC2R, a receptor for the pituitary hormone ACTH.

262 d in heme transport, plays a novel role as a receptor for the plasma and extracellular matrix protein

263 an cells, and confirm that human ACE2 is the receptor for the recently emerging SARS-CoV-2.

264 e signaling induces expression of the PlexA1 receptor for the repellent Sema6D molecule in corticospi

265 urotrophic receptor (p75NTR) is an important receptor for the role of neurotrophins in modulating bra

266 (ACE2) has been identified as the host entry receptor for the severe acute respiratory syndrome coron

267 tivated receptors (PPARs), PPARgamma, is the receptor for the thiazolidinedione class of anti-diabeti

268 identify the protein ComH as the periplasmic receptor for the transforming DNA during natural transfo

269 he viral S-protein, and soluble forms of the receptor for the virus, angiotensin converting enzyme 2.

270 renal injury, including changes in levels of receptors for the antifibrotic factor PGE2.

271 FcgammaRIIa as the two main responsible IgG receptors for the breaking of immune tolerance of microg

272 e, but not axotomized DRGs, strongly express receptors for the cytokine GM-CSF.

273 4]pyrrole phosphonate-cavitands were used as receptors for the design of supramolecular sensors for c

274 atidylcholine around p24 proteins, which are receptors for the export of GPI-anchored proteins and ha

275 unctionally interact with other G(i)-coupled receptors for the fine tuning of neuronal activity.SIGNI

276 viral mobility by removing the extracellular receptors for the haemagglutinin (HA) glycoprotein.

277 s of multiple species function as cell-entry receptors for the haemagglutinin-like H18 protein of the

278 regulates signal transduction downstream of receptors for the IL-23/IL-12 pathways and type I interf

279 arly imprinted polymer (MIP)-based synthetic receptors for the molecular recognition of neuron specif

280 pecifically described are sex differences in receptors for the stress neuropeptide, corticotropin-rel

281 es proved high specificity of the artificial receptors for the targets.

282 Drug development efforts have targeted both receptors for the treatment of insomnia, circadian rhyth

283 yrosine kinase inhibitors targeting the ErbB receptors for their effects on developing zebrafish ( Da

284 s in a CD62L-dependent way and relied on S1P receptors for their exit.

285 micelles afforded water-soluble nanoparticle receptors for their template molecules.

286 Identification of receptors for these maturation-inducing hormones (MIHs)

287 express Death-receptor 3 (DR3; the only know receptor for TL1A) and stimulation with TL1A induces act

288 investigating the potential of targeting Wnt receptors for treating gastric cancer, and the specific

289 t identified CD18 as a putative cell surface receptor for uptake of live P. aeruginosa However, how b

290 phA2, has been shown to function as an entry receptor for various types of adherent cells, the gH/gL

291 Indeed, individual EEC subtypes carry receptors for various EEC hormones.

292 VANs, located in nodose ganglia, express receptors for various gut-derived peptide signals; howev

293 r left ventricular systolic function; ITGA9 (receptor for VCAM1 [vascular cell protein 1]) and C5 for

294 r of the scavenger receptor superfamily-as a receptor for VEEV.

295 ransferrin receptor 1 (hTfR1) as a host cell receptor for virus entry.

296 Humans lack skin receptors for wetness (i.e. hygroreceptors), yet we pres

297 lenging way, we chose the beta(2)-adrenergic receptor, for which a large number of ligands is already

298 are usually overexpressed or mutated protein receptors for which spatiotemporal regulation differs be

299 Frizzleds (Fzd) are the primary receptors for Wnt morphogens, which are essential regula

300 By contrast, receptors for Zika virus and cytomegalovirus, which caus