ライフサイエンスコーパス: transmembrane receptor

1 oupled receptors (GPCRs, also known as seven-transmembrane receptors).

2 ai signaling module by a cell surface, seven-transmembrane receptor.

3 NA injection by T5 phage upon binding to its transmembrane receptor.

4 i) signaling module by a cell surface, seven-transmembrane receptor.

5 y similar defects as the knockout of the Dcc transmembrane receptor.

6 l guanosine 5'-triphosphatase (GTPase) and a transmembrane receptor.

7 the neuropeptide sensitivity of the neuronal transmembrane receptor.

8 tein that connects the actin cytoskeleton to transmembrane receptors.

9 connections by anchoring actin filaments to transmembrane receptors.

10 ptor tyrosine kinase, and the Frizzled seven-transmembrane receptors.

11 lowing their recruitment to signal-activated transmembrane receptors.

12 c lipids may modulate ectodomain shedding of transmembrane receptors.

13 nly at the carboxyl tails of GPCRs and other transmembrane receptors.

14 degradation, a pathway usually reserved for transmembrane receptors.

15 mains in extracytoplasmic regions in several transmembrane receptors.

16 mily (LRPs) are complex, multimodular type I transmembrane receptors.

17 function are G proteins controlled by seven transmembrane receptors.

18 receptors (GPCRs) are the largest family of transmembrane receptors.

19 (Galpha), most notably by G protein-coupled transmembrane receptors.

20 g pathways initiated by specific nuclear and transmembrane receptors.

21 stributed in the cytoplasmic domains of many transmembrane receptors.

22 In addition to the 7 transmembrane receptor (7TM)-conserved disulfide bridge

23 stin1, which regulates many aspects of seven transmembrane receptor (7TMR) biology, has also been sho

24 Seven-transmembrane receptor (7TMR) signaling is transduced by

25 or (beta 2AR) and other members of the seven-transmembrane receptor (7TMR) superfamily activate G pro

26 Members of the seven-transmembrane receptor (7TMR) superfamily are sequestere

27 ransmitters, and receptors, as well as seven-transmembrane receptor (7TMR)-type putative gustatory re

28 Ubiquitously expressed seven-transmembrane receptors (7TMRs) classically signal throu

29 Seven transmembrane receptors (7TMRs) exert strong regulatory

30 Seven-transmembrane receptors (7TMRs) have evolved in prokaryo

31 estin-mediated signaling downstream of seven transmembrane receptors (7TMRs) is a relatively new para

32 Seven transmembrane receptors (7TMRs), also known as G-protein

33 Seven-transmembrane receptors (7TMRs), also termed G protein-c

34 upled receptors (GPCRs), also known as seven-transmembrane receptors (7TMRs), both by inhibiting clas

35 Seven transmembrane receptors (7TMRs), commonly referred to as

36 ation, and some signaling functions of seven-transmembrane receptors (7TMRs).

37 e important roles in the regulation of seven-transmembrane receptors (7TMRs).

38 both internalization and signaling of seven-transmembrane receptors (7TMRs).

39 ated G protein-coupled receptors, (aka seven-transmembrane receptors, 7TMRs) also mediate 7TMR intern

40 Ligands acting at 7-transmembrane receptors (7TMs) transduce effects on cell

41 e first to reveal, we believe, for any seven-transmembrane receptor, a functional role of ubiquitinat

42 s, and our findings suggest that single pass transmembrane receptors act as GPCRs in plants, challeng

43 , for spatiotemporal control over endogenous transmembrane receptor activation, enabled through the o

44 talin are key steps to initiate the integrin transmembrane receptors' activation, which mediates many

45 med "energy taxis." In Escherichia coli, the transmembrane receptor Aer is the primary energy sensor

46 olic proteins that form complexes with seven-transmembrane receptors after agonist stimulation and ph

47 oinducing peptides (AIPs)) and their cognate transmembrane receptors (AgrCs).

48 Expression of the cellular transmembrane receptor alphavbeta6 integrin is essential

49 that netrin-1 also interacts with the orphan transmembrane receptor amyloid precursor protein (APP).

50 ing cellular cytoprotective functions by a 7-transmembrane receptor and define the biochemical pathwa

51 bilical cord vascular endothelial cells as a transmembrane receptor and may recognize certain bacteri

52 Tissue factor (TF) is a transmembrane receptor and primary initiator of blood co

53 otein expression and activation of NOTCH2, a transmembrane receptor and transcriptional regulator kno

54 structural and signaling scaffold that binds transmembrane receptors and a wide variety of intracellu

55 nctions through binding to ligand-stimulated transmembrane receptors and activating their kinase doma

56 located within the cytoplasmic tails of many transmembrane receptors and associated adaptor proteins

57 mains (IgFLNs), which interact with numerous transmembrane receptors and cytosolic signaling proteins

58 nally important bridging interaction between transmembrane receptors and histidine kinase.

59 Merlin associates with several transmembrane receptors and intracellular proteins servi

60 bly and intracellular trafficking of various transmembrane receptors and ion-transport proteins.

61 d shedding extracellular domains of multiple transmembrane receptors and ligands.

62 IGF actions are mediated by transmembrane receptors and modulated by IGF-binding pro

63 s when extracellular signals are detected by transmembrane receptors and relayed to flagellar motors,

64 Rs) represent one of the largest families of transmembrane receptors and the most common drug target.

65 manner that required selective activation of transmembrane receptors and was distinct from VEGF-A-ind

66 ure accurate trafficking and distribution of transmembrane receptors and/or proteins and their ligand

67 terial MutS), ion transport (cystic fibrosis transmembrane receptor), and mRNA trafficking (yeast Elf

68 Heart of Glass (HEG1), a transmembrane receptor, and Rasip1, an endothelial-speci

69 e last 20 years support the notion that some transmembrane receptors are activated not only by their

70 In many sensory systems, transmembrane receptors are spatially organized in large

71 Transmembrane receptors are the predominant conduit thro

72 ost other cases, it appears that Notch-class transmembrane receptors are ubiquitously expressed.

73 oupled receptors (GPCRs, also known as seven-transmembrane receptors) are typically found at the cell

74 TLRs), widely expressed and highly conserved transmembrane receptors, are at the intersection of diet

75 In this model, Smo acts like many transmembrane receptors associated with cytoplasmic kina

76 response, which involves activation of three transmembrane receptors, ATF6, PERK and IRE1alpha.

77 PAR1 is a biased 7-transmembrane receptor because G proteins mediate thromb

78 ance of C5a receptor [(C5aR)2/C5L2], a seven-transmembrane receptor binding C5a and C5adesArg, remain

79 fat encodes a transmembrane receptor, but post-translational regulatio

80 ntrast to knownGPCRs, however, Arr4 is not a transmembrane receptor,but rather a soluble intracellula

81 Cleavage of transmembrane receptors by gamma-secretase is the final

82 esicles maintain the structural integrity of transmembrane receptors by keeping them in their physiol

83 ation of heterodimeric (alpha/beta) integrin transmembrane receptors by the 270 kDa cytoskeletal prot

84 echanism by which an anti-inflammatory seven-transmembrane receptor can negatively regulate JAK/STAT

85 e recent discoveries reveal the existence of transmembrane receptors capable of responding to steroid

86 rotein is necessary for transit of selective transmembrane receptor cargo by the COPII coat for anter

87 CCL21 are endogenous agonists for the seven-transmembrane receptor CCR7.

88 l. published in Nature demonstrates that the transmembrane receptor CD38 plays a critical role in reg

89 d for several genes, including those for the transmembrane receptor CD44 (CD44 [rs507230]; P = 3.98 x

90 ar carbohydrate-binding domain of the Type I transmembrane receptor CD44 is known to undergo affinity

91 nce suggests that interactions involving the transmembrane receptor CD44 may play an important role i

92 CRT together with the transmembrane receptor CD91 function at the cell membran

93 way as a result of defective cystic fibrosis transmembrane receptor (CFTR) expression and function.

94 d for inferring the functional properties of transmembrane receptor clusters from their structure.

95 ndothelial growth factor receptor, Flt1 is a transmembrane receptor co-expressed with an alternate tr

96 Integrins are transmembrane receptors composed of alpha and beta subun

97 Integrins are transmembrane receptors composed of one alpha subunit an

98 Integrins are heterodimeric transmembrane receptors consisting of alpha and beta sub

99 and detect their concentration via the AgrC transmembrane receptor, coordinating local bacterial pop

100 biogenic amine ligands folds deeply into the transmembrane receptor core where the binding of cis-ret

101 Here, we show that a transmembrane receptor, DCC, forms a binding complex con

102 Here we show that netrin-1 via its transmembrane receptors, deleted in colorectal cancer an

103 Notch transmembrane receptors direct essential cellular proces

104 and through the neuronal leucine-rich repeat transmembrane receptor DMA-1 on sensory dendrites.

105 kin, SAX-7/L1CAM and MNR-1, and the neuronal transmembrane receptor DMA-1.

106 norhabditis elegans through the leucine-rich transmembrane receptor DMA-1/LRR-TM expressed on PVD neu

107 peptide ligand that binds and activates the transmembrane receptor domain, eliciting a cellular casc

108 ators interact with aromatic residues in the transmembrane receptor domain.

109 hat are involved in the glycosylation of the transmembrane receptor dystroglycan.

110 including the upregulated expression of the transmembrane receptor endosialin (CD248).

111 The gene identified encodes a putative transmembrane receptor expressed in all tissues capable

112 eptors (MORs) are members of the large seven-transmembrane receptor family which transduce the effect

113 nergic receptors (betaARs), members of the 7 transmembrane receptor family, have classically been sho

114 d be developed for multiple members of the 7 transmembrane receptor family.

115 llular loops in structural studies of this 7 transmembrane receptor family.

116 We showed that the seven-transmembrane receptor fAR1 is required for folic acid-m

117 ved signaling node comprising a prototypical transmembrane receptor for c-di-GMP, LapD, and a cognate

118 Here we report that the CD44, a transmembrane receptor for hyaluronan, modulates synapti

119 signal phosphatidylserine (PS), a phagocytic transmembrane receptor for PS has proved elusive.

120 ranslocation disrupts ROBO2, which encodes a transmembrane receptor for SLIT ligand, and produces dom

121 Mice lacking the CD44 transmembrane receptor for the glycosaminoglycan hyaluro

122 or-like tyrosine kinase (RYK) functions as a transmembrane receptor for the Wnt family of secreted pr

123 The activin receptor type IIB (ActRIIB) is a transmembrane receptor for transforming growth factor-be

124 radation of bri1-9 and bri1-5, two defective transmembrane receptors for brassinosteroids.

125 The integrins are transmembrane receptors for ECM proteins, and they regul

126 Mammalian plexins constitute a family of transmembrane receptors for semaphorins and represent cr

127 The internalization of transmembrane receptors from the cell surface plays a ce

128 of a physiological requirement for ER-QC in transmembrane receptor function in plants.

129 milarities and their ability to activate the transmembrane receptor glycoprotein 130 (gp130).

130 In this study, we show that a seven-transmembrane receptor, GPR17, negatively regulates the

131 results provide atomic insight into a type I transmembrane receptor heterocomplex and the mechanism o

132 ggest entry into neuronal stem cells through transmembrane receptors, hijacking cellular signaling to

133 s to reveal the arrangement of the component transmembrane receptors, histidine kinases (CheA) and Ch

134 The repeating ternary units are composed of transmembrane receptors, histidine-kinase CheA, and coup

135 Classic IL-6 signaling is conditioned by the transmembrane receptor (IL-6R) and homodimerization of g

136 ycation end products (RAGE) is a multiligand transmembrane receptor implicated in a number of disease

137 We screened all LRR-containing transmembrane receptors in C. elegans and identified the

138 ch encodes an emerging positive regulator of transmembrane receptors in plants, suppressed the effect

139 show that somatodendritic sorting of various transmembrane receptors in rat hippocampal neurons is me

140 eriments, we investigated the roles of three transmembrane receptors in regulating dorsolateral pathf

141 Members of the plexin family are unique transmembrane receptors in that they interact directly w

142 t spatio-temporal localization of Kremen1, a transmembrane receptor, in the mammalian cochlea, and in

143 These seven transmembrane receptors include Gr5a and at least one me

144 le photocontrol of the clustering of diverse transmembrane receptors including fibroblast growth fact

145 onse to the triggering of a diverse array of transmembrane receptors, including antigen receptors.

146 l lamina is linked to the sarcolemma through transmembrane receptors, including integrins and dystrog

147 A variety of transmembrane receptors, including multichain immune rec

148 lasma membrane to cytoskeleton by binding to transmembrane receptor integrin and actin.

149 Activation of transmembrane receptor integrin by talin is essential fo

150 ase (ILK) plays a pivotal role in connecting transmembrane receptor integrin to the actin cytoskeleto

151 Transmembrane receptors interact with extracellular liga

152 Notch1 is an evolutionarily conserved transmembrane receptor involved in melanoma growth.

153 which signals through cAMP, is a melanocytic transmembrane receptor involved in pigmentation, adaptiv

154 Fas is a transmembrane receptor involved in the maintenance of to

155 c embryogenesis receptor kinases (SERKs) are transmembrane receptors involved in plant immunity.

156 Notch are transmembrane receptors involved in the determination of

157 ession requires the RNase activity of the ER transmembrane receptor IRE-1, we developed a potent IRE-

158 The endoplasmic reticulum transmembrane receptor Ire1 senses over-accumulation of

159 In nonneuronal cells, CME of the majority of transmembrane receptors is either directly or indirectly

160 The CD36 family of transmembrane receptors is present across metazoans and

161 Flagellin sensing2 (FLS2) is a transmembrane receptor kinase that activates antimicrobi

162 n AvrPto does so by directly targeting plant transmembrane receptor kinases involved in bacterial per

163 erceived by a protein complex containing two transmembrane receptor kinases, BRASSINOSTEROID INSENSIT

164 Smads, through C-terminal phosphorylation by transmembrane receptor kinases.

165 sduction pathway involving the BRI1 and BAK1 transmembrane receptor kinases.

166 plasmic levels of cyclic-di-GMP activate the transmembrane receptor LapD that in turn recruits the pe

167 Transmembrane receptor-like kinases characterized by the

168 BG1 encodes an Ig-superfamily type I transmembrane receptor-like protein that contains an imm

169 There are many transmembrane receptor-like proteins whose ligands have

170 ntify GRK5/6 as novel kinases for the single transmembrane receptor LRP6 during Wnt signaling.

171 MKS3, encoding the transmembrane receptor meckelin, is mutated in Meckel-Gr

172 Mutations in the gene encoding the single transmembrane receptor multiple epidermal growth factor-

173 to heightened inflammatory responses from CF transmembrane receptor mutant cells and highlight autoph

174 Release of HJV requires it to bind to the transmembrane receptor neogenin.

175 Mice that lack the transmembrane receptor neuropilin-1 (Nrp1), which modula

176 The role of the transmembrane receptor Notch in the adult brain is poorl

177 The transmembrane receptor Notch is used repeatedly during d

178 Signaling through the transmembrane receptor Notch is widely used throughout a

179 microvessels to show that activation of the transmembrane receptor NOTCH1 directly regulates vascula

180 Members of the Notch family of transmembrane receptors, Notch1-4 in mammals, are involv

181 Deleted in colorectal cancer (DCC), a large transmembrane receptor of netrin-1, is critical for medi

182 ike domain containing receptor 1, a putative transmembrane receptor of unknown function.

183 Interaction of transmembrane receptors of the Robo family and the secre

184 The vibrio autoinducer molecules bind to transmembrane receptors of the two-component histidine s

185 Atypical 7-transmembrane receptors, often called decoy receptors, a

186 th the binding of a chemical attractant to a transmembrane receptor on the cell surface.

187 (mRNA) expression of Indian Hh, a ligand of transmembrane receptor patched 1, was 184x higher in BE

188 d in a non-redundant fashion with the Draper transmembrane receptor pathway: loss of either pathway f

189 Cell transmembrane receptors play a key role in the detection

190 We show here that the transmembrane receptor Plexin-B2 is expressed by prolife

191 , renal tubular epithelial cells lacking the transmembrane receptor Plexin-B2 or its semaphorin ligan

192 orin 3E (Sema3E), acts through a single-pass transmembrane receptor, plexin D1, to provide a repulsiv

193 s undergoes structural rearrangements as the transmembrane receptor protein is activated.

194 The transmembrane receptor protein neuropilin 1 (Nrp1) was r

195 learning rate, of the collagen formation and transmembrane receptor protein tyrosine kinase activity

196 proliferation, regulation of transcription, transmembrane receptor protein tyrosine kinase signaling

197 positional cloning and report it to encode a transmembrane receptor protein with two hypervariable ex

198 Transmembrane receptors recognize conserved pathogen-ass

199 The Toll family of class I transmembrane receptors recognizes and responds to diver

200 erial chemotaxis signaling cluster, in which transmembrane receptors regulate CheA autokinase activit

201 homodimerization and heterodimerization of 7-transmembrane receptors regulate processes including spe

202 RIIa) has been identified as an ITAM-bearing transmembrane receptor responsible for mediating "outsid

203 These arrays can be formed around transmembrane receptors, resulting in arrays embedded in

204 Applying our approach to integrin transmembrane receptors revealed a spatial density gradi

205 The secreted protein, Slit2, and its transmembrane receptor, Robo-1, repel neuronal migration

206 ted neurorepellent Slit2, acting through its transmembrane receptor, Roundabout (Robo)-1, inhibits ch

207 discovery over 20 years ago, eukaryotic-like transmembrane receptor Ser/Thr protein kinases (STPKs) h

208 ondins (TSP or THBS) and the Notch family of transmembrane receptors share a role in multiple, overla

209 Members of the Frizzled family of sevenpass transmembrane receptors signal via the canonical Wnt pat

210 ce of membrane nanodomains in the control of transmembrane receptor signaling in vivo.

211 ents of signal transduction, cell cycle, and transmembrane receptor signaling pathways.

212 overed for their role in desensitizing seven-transmembrane receptor signaling via the heterotrimeric

213 how membrane nanoscale organization controls transmembrane receptors signaling activity remains a cha

214 ted that these glycoproteins would influence transmembrane receptor spatial organization and function

215 Lu, an Ig superfamily transmembrane receptor specific for laminin alpha5, is a

216 However, signaling via the transmembrane receptor ST2 and documented caspase-depend

217 been clarified despite recent advances in 7 transmembrane receptor structural biology.

218 Signaling by transmembrane receptors such as G protein-coupled recept

219 pattern recognition receptors-which include transmembrane receptors such as toll-like receptors (TLR

220 " Their receptors are part of a larger seven-transmembrane receptor superfamily, commonly referred to

221 nd colleagues have identified a novel 17-kDa transmembrane receptor, termed Plg-R(KT), that binds pla

222 are signalling molecules, which activate the transmembrane receptor TGR5 and the nuclear receptor FXR

223 Podoplanin (PDPN) is a transmembrane receptor that affects the activities of Rh

224 ycation end products (RAGE) is a multiligand transmembrane receptor that can undergo proteolysis at t

225 The Nogo-B receptor (NgBR) is a transmembrane receptor that contains a conserved hydroph

226 Notch is a transmembrane receptor that controls a diverse array of

227 GPER is a G(s)-coupled seven-transmembrane receptor that has been linked to specific

228 RET encodes a transmembrane receptor that is 20 exons long and produce

229 The Notch gene encodes a transmembrane receptor that is cleaved upon activation,

230 (Spz) into the activating ligand for Toll, a transmembrane receptor that is distributed throughout th

231 GPR119 is a 7-transmembrane receptor that is expressed in the enteroen

232 ate Cyclase C (GC-C) is an apically-oriented transmembrane receptor that is expressed on epithelial c

233 Guanylate cyclase C (GC-C) is a transmembrane receptor that is expressed primarily on in

234 ial cells, guanylyl cyclase 2C (GUCY2C) is a transmembrane receptor that makes cGMP in response to th

235 Cadherin is a cell-surface transmembrane receptor that mediates calcium-dependent c

236 AIL-R1; also known as death receptor 4) is a transmembrane receptor that mediates TRAIL-induced apopt

237 ked peptidoglycan, suggesting that PrkC is a transmembrane receptor that monitors the integrity of th

238 PlexinD1, a transmembrane receptor that regulates neuronal and cardi

239 Robo4 is an endothelial-specific transmembrane receptor that stabilizes the vasculature,

240 eceptor 5 (DR5) is a death domain-containing transmembrane receptor that triggers apoptosis upon bind

241 eptor (LIMR)-type proteins are putative nine-transmembrane receptors that are evolutionarily conserve

242 Integrins are heterodimeric, transmembrane receptors that are expressed in all cells,

243 Unlike many transmembrane receptors that belong to large, extensivel

244 Neuropilins (NRPs) are transmembrane receptors that bind class 3 semaphorins an

245 Plexins are single-pass transmembrane receptors that bind the axon guidance mole

246 CD44 comprises a family of transmembrane receptors that can give rise to multiple C

247 Notch proteins are a family of transmembrane receptors that coordinate binary cell fate

248 Plexins are the first known transmembrane receptors that interact directly with smal

249 Notch family members are transmembrane receptors that mediate essential developme

250 TPsigma) and its subfamily member LAR act as transmembrane receptors that mediate growth inhibition o

251 Cadherins are transmembrane receptors that mediate intercellular adhes

252 Integrins are bidirectional, allosteric transmembrane receptors that play a central role in hemo

253 TLRs are pattern recognition transmembrane receptors that play key roles in innate im

254 Notch receptors are transmembrane receptors that regulate cell fate decision

255 Plexins are transmembrane receptors that regulate processes such as

256 ryotic organisms, where it is often found in transmembrane receptors that regulate two-component sign

257 ycle and signal transduction properties of 7-transmembrane receptors that serve to integrate many bio

258 dulators is controlled by endocytosis of the transmembrane receptors that transduce their effects.

259 are made possible by integrins, a family of transmembrane receptors that, upon binding to the extrac

260 otective signaling stimulated by a typical 7-transmembrane receptor the angiotensin ATII 1A receptor,

261 (interactome) as modulated by a model seven-transmembrane receptor, the angiotensin II type 1a recep

262 l lattice formed from three core proteins: a transmembrane receptor, the His kinase CheA, and the ada

263 in is one of the most mechanistically direct transmembrane receptors-the intracellular domain contain

264 aling proteins, cytoskeletal components, and transmembrane receptors, thereby serving as a scaffold t

265 The primary initiator of coagulation, the transmembrane receptor tissue factor (TF), has gained co

266 nditionally induced by agonists of Toll-like transmembrane receptors (TLR).

267 nteractions that promoted the endocytosis of transmembrane receptors, TLR4 was selected as cargo for

268 After internalization, transmembrane receptors (TMRs) are typically recycled ba

269 Trafficking of transmembrane receptors to a specific intracellular comp

270 is a highly conserved kinase cascade linking transmembrane receptors to downstream effector mechanism

271 s relay extracellular cues from heptahelical transmembrane receptors to downstream effector molecules

272 s of studies, namely the propensity of seven transmembrane receptors to form dimers and thus demonstr

273 chestrate efficient sorting of ubiquitinated transmembrane receptors to lysosomes via multivesicular

274 extracellular microenvironment by anchoring transmembrane receptors to the actin filaments.

275 Filamin-mediated linkages between transmembrane receptors (TR) and the actin cytoskeleton

276 The Notch family of transmembrane receptors transduce extracellular signals

277 vity upon binding to either or both distinct transmembrane receptors TrkA and p75(NTR).

278 wth factor engages two structurally distinct transmembrane receptors, TrkA and p75, which have been p

279 TrkA is a cell surface transmembrane receptor tyrosine kinase for nerve growth

280 mutations and amplification of the type III transmembrane receptor tyrosine kinase KIT.

281 VEGFR-3 is a transmembrane receptor tyrosine kinase that is activated

282 ErbB4, a type I transmembrane receptor tyrosine kinase, is a member of t

283 or receptor (EGFR) is a heavily glycosylated transmembrane receptor tyrosine kinase.

284 Here we show that the transmembrane receptor tyrosine phosphatase Leukocyte-an

285 Epidermal growth factor receptor (EGFR) is a transmembrane receptor-tyrosine kinase that is associate

286 protein coupling of agonist-activated seven-transmembrane receptors, ultimately resulting in recepto

287 Dimerization of single span transmembrane receptors underlies their mechanism of act

288 -unstimulated cells overexpressing the seven transmembrane receptor vasopressin 2.

289 RDC3 and ARRDC4 upon activation of the seven transmembrane receptors vasopressin 2 and beta adrenergi

290 pression of Notch3, a member of Notch family transmembrane receptors, was elevated in human cells dur

291 kinase activation and migration evoked by 7-transmembrane receptors were greater than wild type in b

292 Seven transmembrane receptors were originally named and charac

293 eceptor (TLR) gene family consists of type 1 transmembrane receptors, which play essential roles in b

294 FZD5 encodes a transmembrane receptor with a conserved extracellular cy

295 gene encodes an approximately 50 kDa type I transmembrane receptor with an ectodomain containing thr

296 Plexin C1 is a type I transmembrane receptor with intrinsic R-Ras GTPase activ

297 The Kdrb locus encodes a 1361-amino acid transmembrane receptor with strong homology to mammalian

298 f chemokine receptors CXCR4 and CXCR7, two 7-transmembrane receptors with central functions in normal

299 human cytomegalovirus (HCMV)-encoded type I transmembrane receptors with Fcgamma-binding properties

300 herefore hypothesized that preorganizing the transmembrane receptors would potentiate local TGF-beta