ライフサイエンスコーパス: receptor protein

1 to mimic phosphorylated or dephosphorylated receptor protein.

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

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

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

5 ar levels with concomitant reductions of LDL receptor protein.

6 inflammasomes is induced by activation of a receptor protein.

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

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

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

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

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

12 ctioning and the ancestral origins of such a receptor protein.

13 rted X-ray crystal structure of the sigma(1) receptor protein.

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

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

16 rically regulated via different sites on the receptor protein.

17 of the homodimeric transcription factor cAMP receptor protein.

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

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

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

21 glycoproteins to recognize their respective receptor proteins.

22 ucture, and expression of synaptic glutamate receptor proteins.

23 via PDGFRbeta and TbetaRI by stabilizing the receptor proteins.

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

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

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

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

28 are fundamental to signal transduction by Ub receptor proteins.

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

30 sed in the brain compared to other autophagy receptor proteins.

31 covery methods utilize crystal structures of receptor proteins.

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

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

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

35 ylation at the helical domain of transferrin receptor protein 1 promotes conformational changes that

36 rowth and replication, including transferrin receptor protein 1, the amino acid transporters SLC3A2 a

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

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

39 advanced glycation endproducts and Toll-like receptor proteins 2 and 4.

40 In particular, S100A9-mediated NOD-like receptor protein 3 (NLRP3) inflammasome activation direc

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

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

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

44 ta (IL-1beta), which is mediated by Nod-like receptor protein 3 (NLRP3) inflammasome, cathepsin B, an

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

46 e the nucleotide oligomerization domain-like receptor protein 3 (NLRP3) inflammasome.

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

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

49 f the innate immune pathway, e.g. nucleotide receptor protein 3 (NLRP3).

50 cleotide-binding oligomerization domain-like receptor protein 3 (NLRP3).

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

52 tions in the Wnt inhibitor secreted frizzled receptor protein 4 (SFRP4) cause Pyle's disease (OMIM 26

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

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

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

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

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

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

59 both flexibility and adaptation occur among receptor proteins, allowing for complex signaling networ

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

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

62 n pathway that relies on a bacterial-derived receptor protein and provides a viable alternative to in

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

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

65 approaches to identify putative chemosensory receptor proteins and perturb chemotaxis phenotypes in f

66 Receptor complexes are composed of core receptor proteins and receptor-associated proteins, whic

67 ll interaction of these molecules with their receptor proteins and that strategically designed combin

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

69 plasma PCSK9 and resulted in lower LDLR (LDL receptor) protein and increased plasma LDL-C.

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

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

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

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

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

75 the viral spike protein binding to the human receptor protein angiotensin-converting enzyme II (ACE2)

76 Localization of Mel1a receptor protein appeared to be about the same in wild t

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

78 The orthologs of the CO(2) receptor proteins are present in malaria-transmitting mo

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

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

81 otide-binding [NB] leucine-rich repeat [LRR] receptor) proteins are critical for inducing immune resp

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

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

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

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

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

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

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

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

90 oduction of the acinetobactin outer membrane receptor protein BauA.

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

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

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

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

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

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

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

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

99 ranscription activation by cyclic AMP (cAMP) receptor protein (CAP) is the classic paradigm of transc

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

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

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

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

104 The receptor-protein complexes were purified in quantities s

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

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

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

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

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

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

111 i expression was repressed by the cyclic-AMP receptor protein (Crp) and repression required the cycli

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

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

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

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

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

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

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

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

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

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

122 The Escherichia coli cAMP receptor protein, CRP, is a homodimeric global transcrip

123 The receptor protein Dectin-1 recognizes structures found on

124 ucine-rich repeat (NLR) intracellular immune receptor proteins detect pathogens by the presence of pa

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

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

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

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

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

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

136 Adenosine A1 receptor protein expression was significantly upregulate

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

138 expression and increased placental androgen receptor protein expression.

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

140 (CD205), a member of the macrophage mannose receptor protein family, is the prototypic endocytic rec

141 by illuminating the structure of the mannose receptor protein family.

142 r the SCF (Skp-Cul-Fbox) ubiquitin E3-ligase receptor protein Fbxw7alpha (F-box/WD40 7).

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

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

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

149 Several different receptor proteins have been identified that bind monomer

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

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

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

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

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

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

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

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

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

159 es, which contain low numbers of germination receptor proteins in a focus (a germinosome) surrounded

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

161 e studied the turnover mechanism of retinoid receptor proteins in neural stem cells and glioma stem-l

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

165 nt-pai interactions between c-di-AMP and its receptor proteins, including pai-pai, C-H-pai, cation-pa

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

176 The peptide ligand CLAVATA3 (CLV3) and its receptor protein kinase CLAVATA1 (CLV1) maintain stem ce

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 enoyl-coenzyme A reductase, phospholipase A2 receptor, protein kinase C zeta type, tubulin beta-4B cl

180 activity in the PVN, whether endogenous AT1 receptor-protein kinase C (PKC) activity mediates the au

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

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

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

184 lded agonists of G protein-coupled serotonin receptors, protein kinase C agonists, and a microbial me

185 These include RIG-I-like receptors, protein kinase R, oligoadenylate synthases, a

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

187 9 (PCSK9) regulates low density lipoprotein receptor protein levels by diverting it to lysosomes.

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

189 no effects on sperm count and glucocorticoid receptor protein levels within the epididymal tissue of

190 on of Idol increases low-density lipoprotein receptor protein levels, which facilitates Abeta uptake

191 get gene expression, resulting in higher LDL receptor protein levels.

192 Dopamine D2 and dopamine D3 receptors protein levels in the nucleus accumbens, front

193 r kinases (LRR-RK) FLS2 and EFR, and the LRR receptor protein (LRR-RP) receptors RLP23 and RLP42, res

194 served signals, however, their corresponding receptor proteins (LuxR) are highly variable.

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

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

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

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

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

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

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

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

203 ich brought about increased levels of the SA receptor protein NPR1 without induction of NPR1 expressi

204 othalamus (VMHdm/c) that express the nuclear receptor protein NR5A1 (also known as SF1) are necessary

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

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

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

208 Plants use specific receptor proteins on the cell surface to detect host-der

209 or DRP-1 (dynamin-related protein 1) and its receptor proteins on the outer mitochondrial membrane.

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

211 We compared the requirements for autophagy receptor proteins: OPTN, NBR1, p62, NDP52, and TAX1BP1 i

212 s47) was used to identify the mosquito Pfs47 receptor protein (P47Rec) using far-Western analysis.

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

214 ecifically on cargo recognition by autophagy receptor proteins p62 and NBR1 (neighbour of BRCA1) and

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

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

217 se producing trehalose and G-protein coupled receptor proteins, photosynthesis-related enzymes and go

218 ily perceived at the plasma membrane (PM) by receptor proteins, plasmodesmata also cluster receptor-l

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

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

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

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

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

224 Yeast two-hybrid assays involving seven ABA receptor proteins (PtrRCAR) against 12 PtrHAB proteins d

225 Although the innate immune receptor protein, Receptor for Advanced Glycation End pr

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

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

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

229 dopsis thaliana) intracellular innate immune receptor protein RESISTANCE TO PSEUDOMONAS MACULICOLA1 (

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

231 Here, we report our discovery that the ACE2 receptor protein robustly localizes within the motile ci

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

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

234 4% identical to the human and mouse 5-HT(2C) receptor protein sequences.

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

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

237 Targeting receptor proteins, such as ligand-gated ion channels and

238 ediated transcription factors of the nuclear receptor protein superfamily.

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

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

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

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

243 NR2F1 encodes a nuclear receptor protein that regulates transcription.

244 otide binding site Leucine-rich repeat (NLR) receptor protein that was altered in three different mut

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

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

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

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

249 PCRs) are a ubiquitously expressed family of receptor proteins that regulate many physiological funct

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

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

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

253 ctivation of the murine X chromosome-encoded receptor proteins Toll-like receptor (TLR) 7 and TLR8 re

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

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

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

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

258 The non-receptor protein tyrosine phosphatase (PTP) SHP2, encode

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

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

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

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

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

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

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

266 that cytoplasmic BMP10 interacted with both receptor protein tyrosine phosphatase sigma (PTPRS) and

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

268 Receptor protein tyrosine phosphatase sigma (PTPsigma) a

269 Receptor protein tyrosine phosphatase sigma (RPTPsigma)

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

271 neuronal cultures, we demonstrate a role of receptor protein tyrosine phosphatase zeta (RPTPzeta) in

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

273 Receptor protein tyrosine phosphatase-kappa (PTPRK) spec

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

275 Receptor protein tyrosine phosphatases (PTPs) counterbal

276 Receptor protein tyrosine phosphatases (RPTPs) can play

277 Receptor protein tyrosine phosphatases (RPTPs) play crit

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

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

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

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

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

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

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

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

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

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

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

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 nd M(2)-muscarinic receptor mRNA and beta(2)-receptor protein were comparable to SN.

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 drive the final stages of vesi

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