ライフサイエンスコーパス: signaling protein

1 lock to directing trafficking of another key signaling protein.

2 -derived signals in which Hic-5 is a pivotal signaling protein.

3 ctive yellow protein (PYP) is a prototypical signaling protein.

4 vide the first characterization of the SH2D5 signaling protein.

5 ight-induced overexpression of an endogenous signaling protein.

6 trafficking complex and FtsEX cell division signaling protein.

7 otility, cytoskeleton-membrane scaffolds and signaling proteins.

8 t pleckstrin homology (PH) domain-containing signaling proteins.

9 phopeptide recognition modules found in many signaling proteins.

10 , and increased abundance of hepatic insulin signaling proteins.

11 toplasmic domain to expose docking sites for signaling proteins.

12 of both TRAF2 and TRAF3 and TRAF2-associated signaling proteins.

13 cts the phosphorylation state of at least 31 signaling proteins.

14 ane invaginations that can sequester various signaling proteins.

15 lasmic region and recruitment of cytoplasmic signaling proteins.

16 e expression patterns and phosphorylation of signaling proteins.

17 s covalently linked to proteases that cleave signaling proteins.

18 ing from pathological activation of upstream signaling proteins.

19 to the environment by modifying cysteines of signaling proteins.

20 al motif that mediates communication between signaling proteins.

21 nce factor interacts with multiple host cell-signaling proteins.

22 functions by binding and activating cellular signaling proteins.

23 ion at the telencephalic midline mediated by signaling proteins.

24 the oxidoreductases and allied transport and signaling proteins.

25 oupled receptors with regulator of G protein signaling proteins.

26 the unconventional secretion of cytoplasmic signaling proteins.

27 in followed by interactions with cytoplasmic signaling proteins.

28 potentially interact with a distinct set of signaling proteins.

29 osttranslational regulation on cell survival signaling proteins.

30 modynamic barriers for binding of downstream signaling proteins.

31 rolling the expression of genes encoding ABA signaling proteins.

32 tating the functions of poorly characterized signaling proteins.

33 nd regulate the activities of many important signaling proteins.

34 s on a newly quantified gradient in upstream signaling proteins.

35 leoporins, mRNA-processing enzymes, and cell-signaling proteins.

36 lation with phosphorylation of intracellular signaling proteins.

37 and is required for the folding of numerous signaling proteins.

38 in cytoskeleton through numerous adaptor and signaling proteins.

39 elopment of modulators targeting families of signaling proteins.

40 d secretion of the pro-repair WNT1-inducible signaling protein 1 (WISP-1).

41 ed in vitro that tumor-derived Wnt-inducible signaling protein-1 (WISP1) exerts paracrine action to s

42 Cellular response is initiated through a signaling protein (a receptor), which interacts with the

43 ns, body composition by DEXA, tissue insulin signaling protein abundance by Western blotting, glucose

44 sults describe an unprecedented mechanism of signaling protein activation in cancer.

45 be highly nonlinear so that small changes in signaling protein activity can give rise to large change

46 then used the trained tumor model to predict signaling protein activity in a panel of breast cancer c

47 e's protein expression profile, or infer the signaling protein activity, given a tumor sample's gene

48 s, impaired ciliary trafficking of olfactory signaling proteins, adenylate cyclase III (ACIII), and c

49 n NK cells selectively lacking expression of signaling proteins after human cytomegalovirus (HCMV) in

50 or four linear calcium domains that organize signaling proteins along the flagella.

51 These included key CTL effector molecules, signaling proteins and a subset of metabolic enzymes.

52 has an impact on the interaction with other signaling proteins and adds an additional line of comple

53 cells, are packed with information including signaling proteins and both coding and regulatory RNAs,

54 PPKs phosphorylate light-signaling proteins and histones to affect plant developm

55 K autophosphorylation selects the downstream signaling proteins and lipids to effect growth factor an

56 on as intercellular messengers by delivering signaling proteins and noncoding RNAs to alter target ce

57 We analyzed the level of 133 key signaling proteins and phosphoproteins in laser capture

58 ansmission, is modulated by interaction with signaling proteins and post-translational modifications.

59 nstitute the largest family of transmembrane signaling proteins and the largest pool of drug targets,

60 d to directly track the activity of specific signaling proteins and their use is revolutionizing our

61 imately 100 aa that bind phosphotyrosines in signaling proteins and thereby mediate intra- and interm

62 s to explore the roles of C1 domains in many signaling proteins and to better understand their molecu

63 matory control, cell survival, intracellular signaling, protein and lipid homeostasis, and clotting p

64 pression, activation states of intracellular signaling proteins, and cytokine production.

65 ive oxygen species (ROS)-generating enzymes, signaling proteins, and downstream executors such as ion

66 found in eukaryotic phosphate transporters, signaling proteins, and inorganic polyphosphate polymera

67 lls communicate with each other by secreting signaling proteins, and the blood is a key conduit for t

68 Members of the Wnt family of secreted signaling proteins are key regulators of cell migration

69 ns, transcription factors, and intracellular signaling proteins are overrepresented among maintained

70 Although the concentrations of signaling proteins are perturbed in disease states, such

71 their regulatory RGS (Regulator of G-protein Signaling) protein are conserved in all eukaryotes.

72 RGS (regulator of G protein signaling) proteins are negative modulators of the paras

73 acting as a scaffold, recruiting downstream signaling proteins, as well as by proteolytic cleavage o

74 l implants increase the expression of agouti signaling protein (ASIP) mRNA in skin, likely explaining

75 In contrast, MC1R antagonists agouti signaling protein (ASIP) or human beta-defensin 3 (HBD3)

76 feather development or pigmentation: agouti signaling protein (ASIP), follistatin (FST), ecodysplasi

77 gene transcript, and two antagonists, agouti-signaling protein (ASP) and agouti-related protein (AGRP

78 eases with increasing levels of CheA, a core signaling protein associated with the receptors, whereas

79 ffolding protein that interacts with various signaling proteins associated with coordinated regulatio

80 d movement, we imaged various structural and signaling proteins at cell-cell and cell-matrix junction

81 insight into tissue origin and the wiring of signaling proteins at membranes to predict onset and beh

82 The levels of the obligate signaling protein Bcl10 are reduced by RNF181 even prior

83 emes as specialized filopodia that transport signaling proteins between signaling cells.

84 antagonists human beta-defensin 3 and agouti signaling protein blocked MSH- but not forskolin-mediate

85 res reorganization of receptors and membrane signaling proteins, but this spatial regulation is not w

86 lation of kinase activity and recruitment of signaling proteins by activated KIT.

87 orrect distribution and activity of secreted signaling proteins called morphogens is required for man

88 c, subcellular perturbation of an individual signaling protein can help to determine its role in cont

89 re predicts that the translocation rate of a signaling protein can regulate the damping of system osc

90 we focus on mechanochemical feedback, where signaling proteins can establish patterns via coupling t

91 cts of CHK2 were dependent on the downstream signaling proteins CDC25C and CDK1.

92 d preventing the dissociation of chemotactic signaling protein (CheA).

93 onses often involve endosomal trafficking of signaling proteins; coincidently, endosomes serve as sig

94 affold but recruits a distinct repertoire of signaling proteins compared with SgK269.

95 tions and function to scaffold intracellular signaling protein complexes.

96 al docking for mapping dynamics in transient signaling protein complexes.

97 PII signaling proteins comprise one of the most versatile si

98 Signaling proteins comprised of modular domains have evo

99 ases (LRR RLKs) form a large family of plant signaling proteins consisting of an extracellular domain

100 Several classes of signaling proteins contain autoinhibitory domains that p

101 ator previously identified as a synaptogenic signaling protein, contributes to establishing dendrite

102 IQGAP1 interacts with several signaling proteins, cytoskeletal components, and transme

103 Other At-RBP set proteins include major signaling proteins, cytoskeleton-associated proteins, me

104 hosphorylated and associated with downstream signaling proteins, demonstrating that the molecular den

105 of HCV to antagonize mitochondrial antiviral-signaling protein-dependent innate cellular defenses.

106 The glucocorticoid receptor (GR), like many signaling proteins, depends on the Hsp90 molecular chape

107 rs to stimulate the same suite of downstream signaling proteins, different agonists are capable of in

108 aling is a dispersal mechanism that delivers signaling proteins directly at sites of cell-cell contac

109 various partners, including trafficking and signaling proteins, directly to GPCRs, non-visual arrest

110 hosphorylated mTOR and protein kinase B, the signaling proteins downstream of mGlu5 activation, were

111 ling network in HEK293T cells, we analyze 20 signaling proteins during a 1-h EGF stimulation time cou

112 Little is known whether signaling proteins [e.g., G protein-coupled receptors (G

113 stem are controlled by molecules such as the signaling protein endothelin 3 (EDN3), its receptor (the

114 ein level for the downstream survival kinase-signaling proteins Erk and phospho-Erk among groups.

115 Our results suggest that C1ql3 is a signaling protein essential for subsets of synaptic proj

116 here the ethylene receptors and the ethylene signaling protein ETHYLENE-INSENSITIVE2 and REVERSION-TO

117 In Caenorhabditis elegans the signaling protein Exchange Factor for ARF-6 (EFA-6) is a

118 this expectation, we identified 28 candidate signaling proteins expressed during zebrafish embryogene

119 igments, and other phototransduction cascade signaling proteins expressed in these eyes are related t

120 e hypothesized that alterations in glutamate signaling protein expression and co-expression network f

121 The absence of B and myeloid cell-related signaling protein expression in these NK cell subsets co

122 ing converge to induce the expression of the signaling proteins FBJ osteosarcoma oncogene (c-FOS, enc

123 LZF), as well as expression of intracellular signaling proteins FcepsilonRgamma, spleen tyrosine kina

124 s (FKBPs) are pivotal modulators of cellular signaling, protein folding, and gene transcription.

125 n factor NF-kappaB, ubiquitination, cytokine signaling, protein folding, type I interferon production

126 RR systems and coupling a complex network of signaling proteins for cell-fate regulation.

127 assays, we demonstrate that Wnt5 and the PCP signaling proteins Frizzled, Strabismus, and Dishevelled

128 he clustering and activation of caveolin and signaling proteins further stabilize raft structure and

129 in the context of peptides that bind to the signaling protein Galphai1.

130 xpressed in B cells where it associates with signaling proteins Grb2 and Vav1, and is tyrosine phosph

131 en species, ABA biosynthesis, the retrograde signaling protein GUN1, and ABI4.

132 GF-beta and bone morphogenetic protein (BMP) signaling proteins has numerous developmental and physio

133 Further, we show that upstream signaling proteins have abundance-dependent effects on d

134 nase protein family, bacterial transmembrane signaling proteins implicated in the regulation of cell

135 Cdc42 is a signaling protein important for reorganization of actin

136 The stability and activity of numerous signaling proteins in both normal and cancer cells depen

137 eat shock protein 90 (hsp90) associates with signaling proteins in cells including soluble guanylate

138 ion of EphA4 suggest the importance of these signaling proteins in establishing functional auditory c

139 hway composed of the T4P upstream of the Dif signaling proteins in M. xanthus.

140 dehyde dehydrogenase (ALDH) activities and 5 signaling proteins in single MDA-MB-231 breast cancer ce

141 phosphorylated and activated forms of mTORC1 signaling proteins in the prefrontal cortex (PFC).

142 the hope that expression of light-activated signaling proteins in the surviving cells could restore

143 ich have no demonstrated binding domains for signaling proteins in their cytoplasmic tails, nonethele

144 -translational modification of intracellular signaling proteins in these pathways is a key regulatory

145 ng pathway, ubiquitination events on several signaling proteins including HOIL-1 and Tollip were obse

146 chaperone that facilitates the maturation of signaling proteins including many kinases and steroid ho

147 splayed decreased phosphorylation of several signaling proteins including Src and GSK3beta.

148 ake, tyrosine phosphorylation of several key signaling proteins (including the high-affinity IgE rece

149 tion of a multiprotein complex that contains signaling proteins, including beta-catenin.

150 ropagate to the spatial recruitment of early signaling proteins, including spleen tyrosine kinase (Sy

151 cient for multiple transcription factors and signaling proteins, including tyrosine kinase SYK, for w

152 dependent phosphorylation of key endothelial signaling proteins--including endothelial nitric oxide s

153 a signaling network composed of hundreds of signaling proteins interacting with each other extensive

154 mples underscore the utility of the membrane/signaling protein interaction network for gene discovery

155 positive allosteric facilitators of receptor-signaling protein interaction.

156 x 10(6) pairs, we identified 12,102 membrane/signaling protein interactions from Arabidopsis.

157 ies show that the cleavage site of the lipid-signaling protein intermediate bears rigid alpha-helical

158 ongs to a gene superfamily encoding TGF-beta-signaling proteins involved in bone and cartilage biolog

159 -specific ubiquitin ligase atrogin-1 targets signaling proteins involved in cardiac hypertrophy for d

160 However, receptors and downstream signaling proteins involved in TGF-beta1-induced hepcidi

161 mell, its function on a molecular level, the signaling proteins involved in the process and the mecha

162 F-beta) network of ligands and intracellular signaling proteins is a subject of intense interest with

163 structure where the lateral organization of signaling proteins is tightly regulated.

164 ne H2A variant H2AX, gammaH2AX, a DNA damage signaling protein, is possible using (111)In-labeled ant

165 , a negative regulator of multiple oncogenic signaling proteins, is a promising therapeutic approach

166 athic region implicated in interactions with signaling proteins, is crucial for caveola formation.

167 ents comprising 441 transcription factor and signaling protein isoforms across 68 Yoruba (YRI) HapMap

168 e the regulation of short-term growth factor signaling (protein kinase B (PKB/Akt) activity) and long

169 gives rise to MVs, which uniquely contain a signaling protein kinase that helps propagate the transf

170 Allosteric switches introduced into motility signaling proteins (kinases, guanosine triphosphatases,

171 y to probe dissipation in two key classes of signaling proteins: kinases and G-protein-coupled recept

172 tations in human protein kinases, a class of signaling proteins known to be frequently mutated in hum

173 The resulting release of pro-apoptotic signaling proteins leads to cell destruction through act

174 uctural conservation of other death receptor signaling proteins, led us to wonder what would happen i

175 factors (FHFs) are a family of intracellular signaling proteins linked with Nav channel regulation in

176 the function of the mitochondrial antiviral signaling protein MAVS, implicating PB2 in the regulatio

177 unity by cleavage of mitochondrial antiviral signaling protein (MAVS) and T cell protein tyrosine pho

178 and innate immunity, mitochondrial antiviral signaling protein (MAVS) and TRIF, a phosphatase involve

179 VHSV-IVb) suppressed mitochondrial antiviral signaling protein (MAVS) and type I IFN-induced gene exp

180 ed on stimulation of mitochondrial antiviral-signaling protein (MAVS) by the antimicrobial peptide LL

181 The mitochondrial antiviral signaling protein (MAVS) is a central signal transductio

182 (shRNA) knockdown of mitochondrial antiviral signaling protein (MAVS) or interferon regulatory factor

183 egative regulator of mitochondrial antiviral signaling protein (MAVS) that is critical for antiviral

184 gene 1 (RIG-I), and mitochondrial antiviral signaling protein (MAVS), and subsequently induced IFN r

185 specific lesions in mitochondrial antiviral signaling protein (MAVS), interferon regulatory factor 3

186 by TRIM25 and binds mitochondrial antiviral signaling protein (MAVS), leading to the production of t

187 termined the role of mitochondrial antiviral-signaling protein (MAVS), the adaptor protein for RIG-I

188 termined the role of mitochondrial antiviral signaling protein (MAVS), the adaptor protein for RIG-I-

189 of mice deficient in mitochondrial antiviral-signaling protein (MAVS), the signaling adaptor for RNA

190 s are detected via a mitochondrial antiviral signaling protein (MAVS)-dependent RNA sensing pathway o

191 tively regulates the mitochondrial antiviral signaling protein (MAVS)-mediated antiviral responses.

192 modulated the RIG-I/mitochondrial antiviral signaling protein (MAVS)/TBK1/IRF3/interferon-stimulated

193 cid-inducible gene I/mitochondrial antiviral-signaling protein-mediated RNA-sensing pathway.

194 Additionally, mitochondrial antiviral signaling protein-mediated signaling through cytosolic p

195 ansmitter-modulator receptors, ion channels, signaling proteins, neuropeptides and vesicular release

196 The transmembrane signaling protein Notch, which is crucial for embryonic

197 d the spindle assembly checkpoint, acting on signaling proteins of the conserved HORMA domain family.

198 ytometry data sets, measuring intra-cellular signaling proteins of the human immune system and their

199 ribosylation of Smad3 and Smad4, two central signaling proteins of the pathway.

200 ts of pathogenic bacteria include the sensor/signaling proteins of the serine/threonine protein kinas

201 RGS (regulator of G protein signaling) proteins of the R7 subfamily (RGS6, -7, -9, a

202 Studies in mice harboring alterations in TCR signaling proteins or transcriptional regulators have re

203 trains of mice harboring mutations in T cell signaling proteins or transcriptional regulators, conven

204 ts from three phosphorylation sites in three signaling proteins over multiple time points from platel

205 ndent on complement receptor 3 (CR3) and the signaling proteins phosphatidylinositol-3-kinase and cas

206 report a negative feedback loop between the signaling protein phospholipase D (PLD), phosphatidic ac

207 ase in the phosphorylation of the downstream signaling protein, PKC-alpha, and Ca(2+)/calmodulin-depe

208 The role that signaling proteins play to establish a tumor microenviro

209 Endosomal trafficking of signaling proteins plays an essential role in cellular h

210 sorders, rendering them and their downstream signaling proteins potential therapeutic targets.

211 umor growth in part through secretion of the signaling protein prosaposin.

212 termolecular interactions in the multidomain signaling protein, protein kinase Calpha (PKCalpha).

213 rotubule (MT) polymerization dynamics by the signaling proteins Rac1 and stathmin.

214 the adaptor protein mitochondrial antiviral signaling protein, regulates NF-kappaB-mediated inductio

215 The intracellular signaling protein regulator of presynaptic morphology 1

216 ing mechanisms that disperse these morphogen signaling proteins remain controversial.

217 he expression and phosphorylation of insulin signaling proteins remained comparable among APP, ApoE3x

218 bution of membrane receptors, scaffolds, and signaling proteins required for neuronal plasticity.

219 sfer tumor cell derived genetic material and signaling proteins, resulting in e.g. increased tumor an

220 V-1 was determined by phosphorylation of the signaling protein ribosomal S6.

221 KaiB, and KaiC proteins and a set of output signaling proteins, SasA and CikA, which transduce this

222 ocal regulation of the mutually antagonistic signaling proteins, SasA and CikA.

223 2 (Pk2) is a post-synaptic non-canonical Wnt signaling protein shown to interact with post-synaptic d

224 metry, we profiled surface and intracellular signaling proteins simultaneously in millions of healthy

225 SltA and the putative pseudokinase/protease signaling protein SltB comprise a regulatory pathway spe

226 transforming growth factor (TGFbeta) and its signaling protein Smad3, known contributors to IH.

227 that NUP93 and exportin 5 interact with the signaling protein SMAD4 and that NUP93 mutations abrogat

228 Accumulation of the signaling protein Smoothened (Smo) in the membrane of pr

229 living cell provides a platform for receptor signaling, protein sorting, transport, and endocytosis,

230 CR phosphorylation was triggered, downstream signaling proteins spontaneously separated into liquid-l

231 in a manner that requires the presence of a signaling protein Sprouty-2.

232 ons required ALK activity and its downstream signaling proteins STAT3 and C/EBPbeta.

233 0 enhanced activation of the key FcepsilonRI signaling proteins Stat5, JNK, and ERK.

234 The Suppressor of TCR signaling proteins (Sts-1 and Sts-2) are two homologous

235 cent studies we show that alpha7 nAChRs bind signaling proteins such as heterotrimeric GTP-binding pr

236 ty by influencing the activity of downstream signaling proteins such as histidine kinases (HisKa) in

237 Signaling proteins such as protein kinases adopt a diver

238 These included plasma-membrane-localized signaling proteins such as receptor-like kinases, aspart

239 such as IFIT1, IFIT2, and IFIT3, as well as signaling proteins such as STAT1, STAT2, and MAVS, were

240 lated brain regions, and reduced hippocampal signaling proteins, such as brain-derived neurotrophic f

241 nding and activating different intracellular signaling proteins, such as G proteins (Galphabetagamma,

242 so-called CaaX proteins, which includes many signaling proteins, such as most small GTPases.

243 We also found that signaling proteins, such as STAT3, Raf1, and PKCzeta, we

244 We also found that signaling proteins, such as STAT3, Raf1, and PKCzeta, we

245 consistent with the activation of downstream signaling proteins, such as Zap70 and PLC-gamma1.

246 s a ubiquitin-binding autophagy receptor and signaling protein that accumulates in premalignant liver

247 f three human malignancies, and KSHV K1 is a signaling protein that has been shown to be involved in

248 Angiopoietin-like 4 (ANGPTL4) is a secreted signaling protein that is implicated in cardiovascular d

249 an Eph receptor-class-specific intracellular signaling protein that is required for appropriate neuro

250 collectively suggest that Shp2 is a critical signaling protein that is required to maintain Sertoli c

251 ule-A (JAM-A) is a tight junction-associated signaling protein that regulates epithelial cell prolife

252 activates FLOWERING LOCUS T1 (FT1), a mobile signaling protein that travels from the leaves to the sh

253 Protein kinases are dynamically regulated signaling proteins that act as switches in the cell by p

254 Cilia house signaling proteins that allow the cell to sample their e

255 ly, we show that three critical postsynaptic signaling proteins that bind to the PDZ domains of PSD-9

256 omprise a family of lipid-modified, secreted signaling proteins that control embryogenesis, as well a

257 ory cilia are populated by a select group of signaling proteins that detect environmental stimuli.

258 are small modules present in regulatory and signaling proteins that mediate specific protein-protein

259 Wnt proteins are a family of secreted signaling proteins that play key roles in regulating cel

260 ell and respond by secreting proinflammatory signaling proteins that recruit immune cells to clear th

261 ellular guidance molecules and intracellular signaling proteins that regulate axonal outgrowth and ex

262 Identifying the signaling proteins that regulate LRRK2 function and toxi

263 dentified that polarizes the distribution of signaling proteins that restricts growth to cell ends an

264 AT) signalosome and activation of downstream signaling proteins that resulted in reduced adhesion, ag

265 vidence that cells use cytonemes to exchange signaling proteins, that cytoneme-based exchange is esse

266 onco-Dbl-transformed cells contain a unique signaling protein, the ubiquitously expressed non-recept

267 linearly proportional to the activity of the signaling protein they have been engineered to track.

268 f a receptor respond to different ligands or signaling proteins through modulation of fast ps-ns side

269 employ interaction proteomics to uncover the signaling protein TIF1gamma as a specific interactor of

270 protease can cleave mitochondrial antiviral-signaling protein to inactivate the retinoic acid-induci

271 and interacted with mitochondrial antiviral signaling protein to induce type I/III interferons (IFNs

272 fecting the expression of genes encoding ABA signaling proteins to affect ABA sensitivity.

273 rved-region 2 (C2) domains target their host signaling proteins to anionic membranes.

274 li and inputs, using an extraordinary set of signaling proteins to process this information and make

275 hether RSPO-LGR4 is coupled to intracellular signaling proteins to regulate Wnt pathways remains unkn

276 -cell analysis with overexpression of tagged signaling proteins to study the dependence of signaling

277 Indeed, cells in all organisms rely on these signaling proteins to survive and proliferate in unpredi

278 y proteins such as transcription factors and signaling proteins to target genes.

279 rhodopsin, is critical for delivering other signaling proteins to the sensory cilium of photorecepto

280 Membrane signaling proteins transduce information across lipid bi

281 ecapentaplegic (Dpp), a Drosophila morphogen signaling protein, transfers directly at synapses made a

282 late additional mutations affecting JAK/STAT signaling, protein translation, and epigenetic control,

283 attenuated in mice deficient for the IFNbeta signaling protein TRIF.

284 hose of mTOR (mammalian target of rapamycin) signaling proteins ULK1 and S6K.

285 e cell type-specific time course response of signaling proteins under unseen perturbations.

286 Protocadherins (Pcdhs) are cell adhesion and signaling proteins used by neurons to develop and mainta

287 We have examined the transport of one PCP signaling protein, Vangl2, from the trans Golgi network

288 egulates the biological activity of numerous signaling proteins via sugar-protein interactions.

289 carbonic anhydrase, stress, degradation and signaling proteins were more abundant while proteins ass

290 Using these models, we also identify which signaling proteins were useful in predicting patient the

291 several genes, including those encoding key signaling proteins, were up-regulated by KGN.

292 tochondrial function and alter intracellular signaling proteins, which can lead to myocyte apoptosis.

293 GTPases are central cellular signaling proteins, which cycle between a GDP-bound inac

294 elopmental factors is a robust repertoire of signaling proteins, which have arisen from extensive gen

295 cellular signaling and is thought to provide signaling proteins with additional regulatory mechanisms

296 ach synthetase is converted into several new signaling proteins with biological activities "orthogona

297 We investigated the association of signaling proteins with epidermal growth factor (EGF) re

298 , and -beta3, are small secreted homodimeric signaling proteins with essential roles in regulating th

299 iate fitting models of a GFP tagged secreted signaling protein, Wnt3, in live zebrafish embryos, whic

300 tes markedly increased the expression of Wnt signaling proteins (Wnt3a, Wnt5a, Wnt10b, LRP5, and beta