ライフサイエンスコーパス: receptor protein

1 ects selection for proper folding of the TCR receptor protein.

2 ar levels with concomitant reductions of LDL receptor protein.

3 inflammasomes is induced by activation of a receptor protein.

4 eceptors or to bridge different parts of one receptor protein.

5 t not for expression of the aryl hydrocarbon receptor protein.

6 ing site and the allosteric vestibule of the receptor protein.

7 that Axl was the most abundantly induced TAM receptor protein.

8 of a single signaling molecule with a single receptor protein.

9 rically regulated via different sites on the receptor protein.

10 of the homodimeric transcription factor cAMP receptor protein.

11 have opposing effects on the activity of the receptor protein.

12 s are mediated by its binding to the LANCL-2 receptor protein.

13 to mimic phosphorylated or dephosphorylated receptor protein.

14 g elevated levels of the RON tyrosine kinase receptor protein.

15 he amino terminal domain (ATD) of the hmGlu2 receptor protein.

16 o an unstable, truncated, and non-functional receptor protein.

17 glycoproteins to recognize their respective receptor proteins.

18 ucture, and expression of synaptic glutamate receptor proteins.

19 via PDGFRbeta and TbetaRI by stabilizing the receptor proteins.

20 ATP-gated behavior of SF2 RNA helicases and receptor proteins.

21 otide-binding site leucine-rich repeat (NLR) receptor proteins.

22 s play key signaling roles in many bacterial receptor proteins.

23 rt the hypothesis that rGC proteins are salt receptor proteins.

24 LATORY COMPONENTS OF ABA RECEPTOR (PYR/RCAR) receptor proteins.

25 ce of one or more of five pro-survival Bcl-2 receptor proteins.

26 are fundamental to signal transduction by Ub receptor proteins.

27 ence in the evolutionary path of the steroid receptor proteins.

28 CTD code--to a large ensemble of CTD-binding receptor proteins.

29 d signaling of the corresponding full-length receptor proteins.

30 of APP mediates interaction of APP with Nogo receptor proteins.

31 r layers as a result of chaperone binding to receptor proteins.

32 ress only one of several alternative sensory receptor proteins.

33 , indicating that CheD may also modulate the receptor proteins.

34 omain in their S proteins to recognize their receptor proteins.

35 n signalling for the control of PD-1 and TNF receptor proteins.

36 oVs in groups B and C bind to their specific receptor proteins.

37 Low-density lipoprotein receptor protein 1 exerts antiatherogenic effects via pa

38 fection of the antagonists secreted frizzled receptor protein-1 or dickkopf-1 produced the opposite e

39 One such receptor system is the NK cell receptor protein-1B (NKR-P1B) and its ligand C-type lect

40 T lymphocytes through induction of Nod-like receptor protein 3 (NLRP3) inflammasome complexes.

41 de-binding oligomerization domain (NOD)-like receptor protein 3 (NLRP3) inflammasome to recruit the a

42 nhibition of a major product of the Nod-like receptor protein 3 (NLRP3) inflammasome with canakinumab

43 tivation of innate immunity induced Nod-like receptor protein 3 (NLRP3) inflammasome-independent and

44 ed on nucleotide oligomerization domain-like receptor protein 3 (NLRP3) triggers endothelial inflamma

45 erial clearance, and we showed that Nod-like receptor protein 3 (NLRP3), apoptosis-associated speck-l

46 The TLR2 ligand increased Nod-like receptor protein 3, an inflammasome component, in Kupffe

47 protein, (3) coronary arteriole leptin (ob) receptor protein, (4) phosphorylated signal transducer a

48 -like transcription factor-1(ELK1) and Death Receptor protein-5 (DR5) in HCC.

49 After PD treatment POS receptor protein abundance and phagocytosis show a coinc

50 ocorticoid receptor; however, glucocorticoid receptor protein abundance was unaffected in miR-433 dec

51 calcium channels and postsynaptic glutamate receptor proteins across the synaptic cleft.

52 gative regulator of the NR3C1 glucocorticoid receptor protein activity driving glucocorticoid resista

53 AF-1 is in the N terminus of the receptor protein and AF-2 activity is dependent on helix

54 eductions in hepatic low-density lipoprotein receptor protein and increased plasma low-density lipopr

55 s II HDAC expression and decreased ryanodine receptor protein and miRNAs expression were also observe

56 ch OSN expresses a single functional odorant receptor protein and projects an axon from the sensory e

57 ing the structure-function properties of the receptor protein and the tissue/cell-type-specific PR si

58 ing platforms to mediate interaction between receptor proteins and adaptor and effector molecules to

59 lian lipid transport and plant abscisic acid receptor proteins and are predicted to have cavities for

60 Rs), which are the largest group of membrane receptor proteins and the most common targets of drug th

61 AF-1 is in the N terminus of the receptor protein, and AF-2 activity is dependent on heli

62 nsporter-gating component KtrA as a c-di-AMP receptor protein, and it was further shown that this pro

63 rized at the mRNA level, the localization of receptor protein, and, by inference, of functional recep

64 ving the BfrA, BfrD, and BfrE outer membrane receptor proteins, and although Bordetella pertussis has

65 tivating kinase 1 kinase complex, autophagic receptor proteins, and mammalian Atg8 homologs.

66 However, some non-receptor proteins are also GEFs.

67 d D2 receptor promoters are both active, the receptor proteins are segregated and do not form complex

68 aleimide-sensitive factor attachment protein receptor) proteins are a highly regulated class of membr

69 ld-type plants contain the full-length CERK1 receptor protein as well as a soluble form of the CERK1

70 ion between the heterocyclic oxygen atom and receptor proteins as well as the importance of the linea

71 m Ca(2+)ATPase, phospholamban, and ryanodine receptor proteins, as well as beta-adrenergic receptor d

72 general negative feedback regulation of the receptor proteins, as well as many coreceptors and prote

73 stinctive, tumor type-specific signatures of receptor proteins associated to epithelial-mesenchymal t

74 le of imaging, localizing, and force-loading receptor proteins at high spatiotemporal resolution.

75 ay between binding and unbinding of synaptic receptor proteins at synapses plays an important role in

76 been raised that RS1-Reg binds to different receptor proteins at the TGN, which trigger release of v

77 d spectroscopy of flavoproteins and lumazine receptor proteins at unprecedented resolution.

78 s of the ferric acinetobactin outer membrane receptor protein BauA while not affecting the production

79 oduction of the acinetobactin outer membrane receptor protein BauA.

80 In general, the large majority of receptor proteins became inserted in the bacterial membr

81 pheromones bind to and modulate activity of receptor proteins belonging to the Rgg family of transcr

82 Soluble extracellular Siglec-E receptor protein bound to the neural glycocalyx.

83 olar epithelial cells expressed lethal toxin receptor protein, bound the protective antigen component

84 ition of pheromone peptides by corresponding receptor proteins, but clear patterns of diversification

85 The expression of CB2 receptor protein by both neurones and microglia in the s

86 ary signaling molecules act through specific receptor proteins by direct binding to alter their activ

87 vitro, the demonstration that distinct mGlu receptor proteins can form heterodimers or hetero-comple

88 The cyclic adenosine 3',5'-monophosphate receptor protein (CAP), a classic activator, is able to

89 envelope glycoprotein gp120 and the cellular receptor protein CD4.

90 We found that the extracellular plant immune receptor protein Cf-2 of the red currant tomato (Solanum

91 isomes (pexophagy) through the assembly of a receptor protein complex (RPC).

92 ation and in the recruitment of Atg11 to the receptor protein complex.

93 The receptor-protein complexes were purified in quantities s

94 onal activity of glucocorticoid and androgen receptor-protein complexes.

95 then recovery suggesting that diminution in receptor proteins contributes to the phagocytic defect.

96 s exported out of the nucleus by the nuclear receptor protein crm-1.

97 ing sites of Mycobacterium tuberculosis cAMP receptor protein (CRP(Mt)) at endogenous expression leve

98 The Escherichia coli cAMP receptor protein (CRP) activates transcription initiatio

99 atory molecules, including cyclic AMP (cAMP) receptor protein (CRP) and c-di-GMP, were substantially

100 ch diverse DNA-binding molecules as the cAMP receptor protein (CRP) and Din-family site-specific seri

101 operons are regulated by LsrR and cyclic AMP receptor protein (CRP) and that proper regulation of the

102 he structural homology of PrfA with the cAMP receptor protein (Crp) and the finding of constitutively

103 eflects regulation of feaR by the cyclic AMP receptor protein (CRP) and the nitrogen assimilation con

104 equences resembling the consensus cyclic AMP receptor protein (CRP) binding site were identified in t

105 We show that the cAMP receptor protein (Crp) binds to DNA as several different

106 In the transcription factor cAMP receptor protein (CRP) from Escherichia coli, the allost

107 sponsive protein (Lrp) and cyclic AMP (cAMP) receptor protein (CRP) in the transcriptional activation

108 The cyclic AMP (cAMP) receptor protein (CRP) indirectly increases ltxA express

109 A homologue of the Escherichia coli cAMP receptor protein (CRP) is linked to the guanylyl cyclase

110 herichia coli, the transcription factor cAMP receptor protein (CRP) is responsible for much of this r

111 Escherichia coli cyclic-AMP receptor protein (CRP) represents one of the paradigms o

112 FixK2 belongs to the cAMP receptor protein (CRP) superfamily.

113 nscription by a mechanism that requires cAMP receptor protein (CRP), cyclic AMP (cAMP) and a CRP-S si

114 interacts with the transcription factor cAMP receptor protein (CRP), forming active cAMP-CRP complexe

115 us to the Escherichia coli cyclic AMP (cAMP) receptor protein (CRP), regulates many aspects of virule

116 A cyclic AMP receptor protein (CRP)-binding site (viz.

117 in response to glucose by cyclic AMP (cAMP) receptor protein (CRP).

118 ctions using the Escherichia coli cyclic AMP receptor protein (CRP).

119 inding protein like its homologue cyclic AMP receptor protein (CRP).

120 level of transcription by cyclic AMP (cAMP) receptor protein (CRP).

121 The receptor protein Dectin-1 recognizes structures found on

122 lass I (lac) and class II (galP1) cyclic AMP receptor protein-dependent promoters.

123 No receptor protein directly mediating phototransduction in

124 ut is likely to require interactions between receptor proteins displayed on their surface.

125 aleimide-sensitive factor attachment protein receptor) proteins drive vesicle fusion in all eukaryote

126 -sensitive factor protein attachment protein receptor) proteins drive vesicle traffic, delivering mem

127 show that BES1 interacts with the ubiquitin receptor protein DSK2 and is targeted to the autophagy p

128 ertain SNARE (soluble NSF attachment protein receptor) proteins ensures the fusion of appropriate ves

129 GPR148 encodes a G-protein-coupled receptor protein expressed in the brain and testes.

130 CLAVATA1 (CLV1) is a receptor protein expressed in the shoot apical meristem

131 A-treated rats correlated with decreased CB1 receptor protein expression and function in the RVM.

132 tated 231 G521R ER cells despite appropriate receptor protein expression and nuclear localization.

133 tudy revealed a 3-fold RA-to-LA adenosine A1 receptor protein expression gradient in the human heart,

134 This was supported by an increase of NR2B receptor protein expression in both the dorsal root gang

135 TRPV1 receptor protein expression in the vagal complex was una

136 Previous studies showed that brainstem 5-HT receptor protein expression was abnormal in DBA/2 mice.

137 A significant 20% reduction in hepatic LDL receptor protein expression was also observed with empag

138 Adenosine A1 receptor protein expression was significantly upregulate

139 n lowered plasma PCSK9 levels, increased LDL receptor protein expression, and restored plasma cholest

140 expression and increased placental androgen receptor protein expression.

141 (GPCR) family is one of the largest membrane receptor protein families and controls many key physiolo

142 ons between specific targeting sequences and receptor proteins, followed by protein translocation acr

143 gs demonstrate that SDC1 serves as the major receptor protein for HCV attachment to cells, providing

144 studies demonstrates that SDC1 is the major receptor protein for HCV attachment.

145 GIV (a.k.a Girdin) was the first non-receptor protein for which the GEF activity was ascribed

146 How viruses evolve to select their receptor proteins for host cell entry is puzzling.

147 ication and can be used to create stabilized receptor proteins for structural and functional studies.

148 aleimide sensitive factor attachment protein receptors) proteins form a complex that drives membrane

149 However, so far no such receptor proteins have been identified for any lantibiot

150 Several different receptor proteins have been identified that bind monomer

151 t may be shared by SR-BI and CD36, scavenger receptor proteins highly homologous to LIMP-2.

152 ed with elevated expression of the IFN-gamma receptor protein IFNGR2.

153 Despite the diversity of the Fc receptor proteins, IgG ligands, and potential responding

154 ge, of PDEs directly interacting with a cAMP-receptor protein in a mammalian system, and highlights a

155 s us to compare the expression profiles of a receptor protein in natural killer cells among donors in

156 has been suggested to operate as a scaffold/receptor protein in neurons, participating in both physi

157 e HER2 mimotope as a substitute for the HER2 receptor protein in piezoimmunosensor or quartz crystal

158 earlier in vivo work for identification of a receptor protein in the aphid gut called aminopeptidase

159 he femoral artery for 72 h increased the EP4 receptor protein in the L4 and L5 dorsal root ganglia ov

160 Neurons with the orexin 1 receptor protein in the ventral C3-5 cervical cord were

161 ing and abrogated expression for each of the receptor proteins in different cell lines.

162 ctionally asymmetric expression of gustatory receptor proteins in the ASE neurons and the antisymmetr

163 nd the antisymmetric expression of olfactory receptor proteins in the AWC neurons.

164 Therefore, expression of 5-HT receptor proteins in the medial-caudal brainstem of DBA/

165 Chemosensory receptor proteins, including odorant receptors (ORs), gu

166 Type I transmembrane AMPA receptor proteins increase the number of AMPA receptor o

167 Type I transmembrane AMPA receptor proteins increase the number of AMPA receptor o

168 nerate a Boolean model of the glucocorticoid receptor protein interaction network that encapsulates f

169 To explore the importance of receptor-protein interactions, we conducted yeast two-hy

170 transcription factor NF-kappaB or toll-like receptor proteins IRAK1 and TRAF6.

171 ructural rearrangements as the transmembrane receptor protein is activated.

172 llular peptides by plasma membrane-localized receptor proteins is commonly used in signal transductio

173 leucine-rich repeat containing, or NOD-like receptor) proteins is in inflammasome activation, which

174 ween critical residues in CytR and CRP (cAMP receptor protein), is disrupted by exogenous cytidine.

175 ttaching the ADP-ribose polymer chain to the receptor protein, is a unique posttranslational modifica

176 of tools to specifically detect and quantify receptor protein isoforms is a major impediment to funct

177 AHA2 localization in a knockout mutant of a receptor protein kinase, FERONIA, we found that the intr

178 lial growth factor homology domains-2 (TIE2) receptor, protein kinase B, and Erk1,2 phosphorylation d

179 show that stimulation of alpha(1)-adrenergic receptor-protein kinase D1-Rem1 signaling increases tran

180 ylated in response to dopamine acting via D1 receptor/protein kinase A (PKA) signaling.

181 wo ubiquitously expressed intracellular cAMP receptors, protein kinase A (PKA) and exchange protein d

182 C albicans was strictly dependent on Fcgamma receptors, protein kinase C (PKC), and reactive oxygen s

183 ane and intracellular ion channels, membrane receptors, protein kinases, protein phosphatases and pro

184 R gene (OPRM1 A118G) has been shown to alter receptor protein level in preclinical models and smoking

185 Furthermore, in HH D1 receptor protein levels are decreased in several brain r

186 9 (PCSK9) regulates low density lipoprotein receptor protein levels by diverting it to lysosomes.

187 oid hamsters (EH), HH exhibited decreased D1 receptor protein levels in carotid bodies, striatum, and

188 ometry showed that overall CB(1) cannabinoid receptor protein levels in the hippocampi of patients wi

189 As well as the expected effects on LDL-receptor protein levels in the liver, mice expressing th

190 esulted in the elevation of beta2-adrenergic receptor protein levels leading to the hyperactivation o

191 ct area, oxidative stress parameters, and ET receptor protein levels.

192 or taste coding in larvae, in which distinct receptor proteins mediate different responses within the

193 aleimide sensitive factor attachment protein receptor) proteins mediate evoked synchronous neurotrans

194 aleimide-sensitive factor attachment protein receptor) proteins mediate fusion by pulling biological

195 f POS was measured by flow cytometry and POS receptor proteins (Mer tyrosine kinase receptor [MerTK]

196 nduced by drug administration, the glutamate-receptor protein metabotropic glutamate receptor 5 (mGlu

197 The transmembrane receptor protein neuropilin 1 (Nrp1) was recently identi

198 we show that a family of proteins named Nogo receptor proteins (NgR1 to NgR3) regulates Abeta product

199 was that sustained activity of the Nod-like receptor protein (NLRP)-3 inflammasome in wounds of diab

200 cleotide-binding oligomerization domain-like receptor protein (NLRP).

201 cleotide-binding oligomerization domain-like receptor protein NLRP3 and subsequently induce inflammas

202 nt transcript 2 (Cdt2) serves as a substrate receptor protein of CRL4.

203 onsist of a recently identified group of ABA receptor proteins of the PYRABACTIN RESISTANCE (PYR)/REG

204 raction of colicin N with its outer membrane receptor protein OmpF.

205 ity remains strictly dependent upon the same receptor proteins (OmpF and TolA) used by full-length co

206 retina survival activity by interacting with receptor proteins on cell surfaces.

207 rent from that found in high affinity solute receptor proteins operating in conjunction with microbia

208 extraordinarily large amounts of the visual receptor protein, opsin.

209 he E3 ligase von Hippel-Lindau and autophagy receptor protein p62 are required for autophagic degrada

210 HH binds to and inactivates the receptor protein patched homolog (PTCH).

211 arrying proteins interact with their cognate receptor protein PEX7 that mediates their transport to p

212 egulated by the interaction of the pheromone receptor protein PrgX with two DNA binding operator site

213 esent the crystal structure of the pheromone receptor protein PrgZ from Enterococcus faecalis in comp

214 s revealed that vaccination with siderophore receptor proteins protects against UTI.

215 eling and computational docking of the virus-receptor protein-protein interaction.

216 can generate shortlists of candidate ligand-receptor protein-protein interactions.

217 e hydrophobic binding region of the sigma(1) receptor protein, regioisomeric spirocyclic thiophenes 9

218 Mechanical forces acting on cell adhesion receptor proteins regulate a range of cellular functions

219 constant in Escherichia coli cAMP-CRP (cAMP receptor protein) regulated gal promoters by in vitro tr

220 er the whole surface of EV and another viral receptor protein remains active.

221 oes and Drosophila, which have related CO(2)-receptor proteins, reveals a pattern of inhibition that

222 to transcriptional control by the cyclic AMP receptor protein, riboswitch-mediated transcription atte

223 ine monophosphate (c-di-GMP) level through a receptor protein RpfR, which contains Per/Arnt/Sim (PAS)

224 ell as of soluble glycoconjugates with their receptor proteins rule fundamental processes in cell bio

225 ns of bacterial surface polysaccharides with receptor protein scaffolds is important for the developm

226 4% identical to the human and mouse 5-HT(2C) receptor protein sequences.

227 mulation of PIP3 in complex with the nuclear receptor protein, SF1, at damage sites requires phosphor

228 N-ethylmaleimide-sensitive factor attachment receptor protein (SNARE) that contains an H3 domain (SNA

229 ediated transcription factors of the nuclear receptor protein superfamily.

230 ffinities of Synechocystis sp. PCC 6803 cAMP receptor protein (SyCrp1), the Escherichia coli Crp (EcC

231 aleimide-sensitive factor activating protein receptor) protein syntaxin 1A.

232 of the crystal structures of the neisserial receptor proteins TbpA and TbpB, each solved in complex

233 TAOK2 interacts with Neuropilin 1 (Nrp1), a receptor protein that binds the secreted guidance cue Se

234 B type 1 (SR-B1), is a multiligand membrane receptor protein that functions as a physiologically rel

235 human UMOD and mouse ZP2, an essential sperm receptor protein that is structurally related to UMOD bu

236 pathway with the widely conserved cyclic-AMP receptor protein that regulates protease production.

237 NR2F1 encodes a nuclear receptor protein that regulates transcription.

238 ation of four Staphylococcus aureus c-di-AMP receptor proteins that are also widely distributed among

239 we will summarize the centrality of Nod-like receptor proteins that assemble inflammasomes and regula

240 nervous system (CNS) disorders, endothelial receptor proteins that control BBB function are poorly d

241 l importance, which implies the existence of receptor proteins that recognize different phosphorylate

242 ceptors (GPCRs) constitute a large family of receptor proteins that sense molecular signals on the ex

243 iquitin (Ub) modifications are transduced by receptor proteins that use Ub-binding domains (UBDs) to

244 In a multimeric receptor protein, the binding of a ligand can modulate t

245 on of a large number of intracellular immune receptor proteins, the majority of which are structurall

246 ch repeat) or ALR (absent in melanoma 2-like receptor) proteins to activate caspase-1 cleavage and in

247 udes a core membrane channel, Toc75, and two receptor proteins, Toc33/34 and Toc159, each containing

248 To identify the presumed receptor proteins, two-hybrid screening was performed.

249 of the collagen formation and transmembrane receptor protein tyrosine kinase activity gene sets with

250 contrast, blocking of both langerin and the receptor protein tyrosine kinase ephrin A2 was required

251 erleukin-2 inducible T cell kinase) is a non-receptor protein tyrosine kinase expressed primarily in

252 rowth factor receptor (also known as Met), a receptor protein tyrosine kinase, is a major regulator o

253 n Dab1, Src and Fyn of the Src-family of non-receptor protein tyrosine kinases, and CrkL) are located

254 r require leukocyte antigen-related (Lar), a receptor protein tyrosine phosphatase (RPTP) and the onl

255 the role of pleiotrophin and its receptors, receptor protein tyrosine phosphatase (RPTPbeta/zeta), a

256 The vascular endothelial (VE) receptor protein tyrosine phosphatase (VE-PTP) associate

257 We investigated the role of IGFBP-2 and receptor protein tyrosine phosphatase beta (RPTPbeta) in

258 By contrast, elevated expression of Lar, a receptor protein tyrosine phosphatase found to be necess

259 One phosphatase that was identified, the receptor protein tyrosine phosphatase leukocyte-antigen-

260 Here we show that the LAR receptor protein tyrosine phosphatase PTP-3 acts with MI

261 o receptors in the brain is regulated by the Receptor Protein Tyrosine Phosphatase RPTP69d.

262 report that within the human immune system, receptor protein tyrosine phosphatase sigma (PTPRS) is e

263 Receptor protein tyrosine phosphatase sigma (PTPsigma) a

264 Receptor protein tyrosine phosphatase sigma (RPTPsigma)

265 CSPGs inhibit nerve regeneration through receptor protein tyrosine phosphatase sigma (RPTPsigma).

266 orkscrew, the drosophila ortholog of the non-receptor protein tyrosine phosphatase type II (SHP2) to

267 hypothesized that the structural features of receptor protein tyrosine phosphatase-gamma (RPTPgamma)

268 Receptor protein tyrosine phosphatase-kappa (PTPRK) spec

269 h the leukocyte common antigen-related (Lar) receptor protein tyrosine phosphatase.

270 interacts with the Ig domains of LAR family receptor protein tyrosine phosphatases (LAR-RPTPs; LAR,

271 Receptor protein tyrosine phosphatases (PTPs) counterbal

272 Receptor protein tyrosine phosphatases (RPTPs) can play

273 le of morphogenetic apoptosis, requiring the receptor protein tyrosine phosphatases (RPTPs): LAR and

274 cans and members of the type IIa subgroup of receptor protein tyrosine phosphatases underlie crucial

275 ing the engaged receptor/ligand complex from receptor protein tyrosine phosphatases with large ectodo

276 enzymes that dephosphorylate STAT3, such as receptor protein tyrosine phosphatases, which are encode

277 that is presumably conserved in all type IIa receptor protein tyrosine phosphatases.

278 ied a suppressor mutation in MOA-1/R155.2, a receptor-protein tyrosine phosphatase, and an enhancer m

279 ErbB family of the receptor protein-tyrosine kinase plays an important role

280 s of the cytoplasmic catalytic domain of the receptor protein-tyrosine phosphatase beta (also known a

281 osphorylation of beta(3) at Tyr(773) through receptor protein-tyrosine phosphatase beta/zeta (RPTPbet

282 g activators of Rac and Rho proteins and the receptor protein-tyrosine phosphatase genes PTPRM and PT

283 Our previous work demonstrated that receptor protein-tyrosine phosphatase zeta (RPTPzeta)/ph

284 ease in the activity of the receptor and non-receptor protein-tyrosine phosphatases that down-regulat

285 IL-34, c-FMS, and a second IL-34 receptor, protein-tyrosine phosphatase zeta (PTP-zeta) w

286 Here, we identify the ubiquitin receptor protein UBASH3B as an important regulator of mi

287 ee evolutionarily diverged ancestral steroid receptor proteins using the Zipping and Assembly Method

288 EP4 receptor protein was present in human and mouse AAA, as

289 The captured receptor protein was then stabilized on the chip surface

290 Whereas the distribution of CGRP receptor proteins was similar in SMCs, RAMP1 associated

291 ication of these widely distributed c-di-AMP receptor proteins we link the c-di-AMP signaling network

292 Both receptor proteins were posttranslationally processed whe

293 pecific in-house generated scFv fragments as receptor proteins were utilised for one step site-direct

294 Drosophila aggression, as well as effects of receptor proteins where relevant data are available.

295 peroxisomes by a concerted action with a co-receptor protein, which in mammals is the PTS1 receptor

296 aleimide sensitive factor attachment protein receptor proteins, which mediate apical (ZG-apical plasm

297 in-like NTD in its spike protein to bind its receptor protein, while HCoV-OC43, another beta-CoV in g

298 ic levels of Oxtr messenger RNA and oxytocin receptor protein with established neuroanatomic methods.

299 rmal accumulation of the pathogenic androgen receptor protein within the nucleus, leading to disrupti

300 The receptor protein WspA, is bioinformatically indistinguis