ライフサイエンスコーパス: binding of @2 to

1 sis of RNA degradome data suggested that the binding of Arabidopsis ARGONAUTE7 to a noncleavable targ

2 pac1 is thought to exert its effects through binding of cAMP leading to a conformational change in Ep

3 Competition between binding of copper ions to a membrane-embedded synthetic

4 They are gated by the binding of cyclic nucleotides to a conserved, intracellu

5 -2 in a substrate-selective manner, with the binding of inhibitor to a single monomer sufficient to i

6 luciferase reporter assays revealed a direct binding of NANOG to a transcriptionally active site in a

7 Binding of raffinose to a carbohydrate-binding protein c

8 Here we show that Hh stimulates the binding of Smo to a plasma membrane-associated kinase Gi

9 y xylose weakens stability, explained by the binding of the glycan to a protein groove.

10 at this blocking activity may originate from binding of the peptide to a sequence of SdrC involved in

11 s 1-101) pull downs showed sixfold-increased binding of vinculin and, to a lesser extent, alpha-actin

12 ion by CatB and the equilibrium constant for binding of CysC to Abeta were determined.

13 d H4 by which ascorbate and BETi blocked the binding of BRD4 to acetylated histones.

14 This analysis highlights that the strong binding of myosin Ic to actin is dominated by the ADP st

15 that Prep1 normally acts by restricting DNA binding of transcription factors to adipogenic enhancers

16 hydrophobic binding plays a main role in the binding of SA to Albumin.

17 ed with Dectin-1 revealed that the forces of binding of Dectin-1 to all of the strains were similar,

18 Insulin further increased binding of MICAL-L2 to alpha-actinin-4 (ACTN4), a protei

19 Strikingly, these results show that binding of MtrF to alpha-Fe2O3 follows a strategy to con

20 op was not required for fibronectin-mediated binding of gp120 to alpha4beta7, nor did V2-specific ant

21 analysis revealed that OA-NO2 increased the binding of Nrf2 to an antioxidant response element in th

22 and enzyme activity are regulated in part by binding of purine nucleotides to an allosteric regulator

23 omal replication fork barrier imposed by the binding of Tus proteins to an array of Ter sites.

24 Binding of Egr3 to and histone methylation at the PGC-1a

25 ecovery phase from a hypoxic injury and that binding of neuronal uPA to astrocytic uPAR induces astro

26 We found that binding of neuronal uPA to astrocytic uPAR promotes astr

27 Particular attention has focused on the binding of plasminogen (Plg) to bacterial surfaces, as i

28 Further, the binding of TLP8 to beta-glucan was dependent on redox.

29 thic helix H10 is responsible for peripheral binding of dimeric tubulin to biomimetic "mitochondrial"

30 r, our studies suggest that PML mediates the binding of PER2 to BMAL1 in the BMAL1/CLOCK heterodimer

31 hPD-1 to hPD-L2 than hPD-L1, and comparable binding of mPD-1 to both ligands.

32 Simultaneous binding of SWR to both H2A nucleosome and free H2A.Z ind

33 Binding of tritiated compounds to brain tissue sections

34 The binding of 16 to BRPF1B was rationalized through an X-ra

35 f Reb A-receptor interaction, as a result of binding of Reb A to BSA, which may ultimately lead to mo

36 affinity than Ca(2+)-free CaM (apoCaM); the binding of CaMKII peptide to CaM in return increases the

37 2 were present in human carotid plaques, and binding of MBL to CC was confirmed in vivo by immunohist

38 emokines, the compounds did not activate G12 Binding of J113863 to CCR2 or CCR5 also induced the recr

39 MP persistence arose secondary to binding of CFH to CD11b, which obstructed the homeostati

40 e metabolic status is reliant upon effective binding of omega1 to CD206.

41 in MDA-MB-231 than MCF-7 potentially due to binding of hyaluronic acid to CD44 expressed by MDA-MB-2

42 e mutant FHR-1 protein strongly competed the binding of FH to cell surfaces, impairing complement reg

43 hat PA50 protects host cells by blocking the binding of TcdA to cell surfaces.

44 )-Cas9 system and measured the quantities of binding of these viruses to cell surfaces.

45 When cells were treated with SMase, the binding of ALO-D4 to cells increased, largely due to inc

46 t, we show that direct, cell-cycle-regulated binding of M18BP1 to CENP-A nucleosomes recruits the Mis

47 in, or phosphorylation site causes excessive binding of RAD51 to CFS loci and impairs CFS expression.

48 ght be advantageous for entropically favored binding of unfolded OMPs to chaperones and, by facilitat

49 An anti-CKAP4 antibody blocked the binding of DKK1 to CKAP4, suppressed AKT activity in a h

50 heat shock protein 90 (HSP90) and stabilizes binding of this chaperone to CMA substrates as they bind

51 ort a model of HCV infection influencing the binding of transcription factors to cognate sites in the

52 We propose that binding of free SC to commensal bacteria is a key and co

53 anges could be explained by predicted direct binding of miRNAs to corresponding mRNAs, suggesting tha

54 Surprisingly, enhanced binding of Hsp90 to CRAF occurs prior to the Ras-CRAF as

55 tudies disclosed the molecular bases for the binding of 19 to CXCR4 and for its improved potency comp

56 Increased binding of QDs to Cyt c results in decreasing fluorescen

57 n the context of dynein alone, we found that binding of LIS1 to DDB does not strongly disrupt process

58 ated Atf1 phosphorylation does not stimulate binding of Atf1 to DNA but, rather, establishes a platfo

59 s conferring a net negative charge disrupted binding of Lon to DNA.

60 e improvements were accompanied by increased binding of MeCP2 T158M to DNA.

61 ic accessory subunit (POLG2), which enhances binding of Pol gamma to DNA and promotes processivity of

62 We show that RLTPR (p.Q575E) increases binding of RLTPR to downstream components of the NF-kapp

63 We hypothesized that blocking the binding of these peptides to DRbeta1-Arg74 could block t

64 The vast majority of mutations do not affect binding of dynein to dynactin and BICD2 and are therefor

65 hat ENb-TRAIL blocks EGFR signalling via the binding of ENb to EGFR which in turn induces DR5 cluster

66 e previously reported that sterols stimulate binding of UBIAD1 to endoplasmic reticulum (ER)-localize

67 Binding of C. albicans to EphA2 on oral epithelial cells

68 Of note, the direct binding of ERalpha-36 to ERK2 prevents its dephosphoryla

69 of band 3 (cdb3-PO4) with Kd = 14 nM; (iii) binding of cdb3-PO4 to erythrocyte membranes is inhibite

70 However, binding of inhibitors to EspD or deletion of EspD itself

71 Binding of PIP2 to ezrin induces a conformational change

72 ise that stereospecific but necessarily weak binding of tropomyosin to F-actin is required for effect

73 The directional and force-stabilized binding of vinculin to F-actin may be a mechanism by whi

74 tes XRCC4 at serines 325/326, which promotes binding of XRCC4 to FBXW7.

75 Binding of IgG Abs to FcgammaRs on immune cells induces

76 The aim of this study was to evaluate the binding of IgE to five recombinant beta-conglutin isofor

77 ith the RGD, but essential to re-enforce the binding of alpha5beta1/alphaIIbbeta3 to FN.

78 Recent structural studies have revealed binding of phosphatidylglycerol lipids to functional imp

79 ing site provide the molecular mechanism for binding of dectin-2 to fungal mannans and also to bacter

80 Binding of TF to FVIIa promotes allosteric conformationa

81 Binding of agonists to G protein-coupled receptors induc

82 Binding of agonists to G-protein-coupled receptors (GPCR

83 s (T1024G and T1086G) abrogated preferential binding of WRN to G4 DNA.

84 Separation-of-function mutations leave the binding of TPX2 to gamma-TuRC intact, whereas branching

85 Binding of Nup153 to gene promoters or transcriptional e

86 nes to form nucleosomes, which restricts the binding of transcription factors to gene regulatory sequ

87 Glycan array analysis confirmed selective binding of the CRD to glycans that contain Manalpha1-2Ma

88 In conclusion, we have shown that binding of UL20 to GODZ in the Golgi apparatus regulates

89 CD4 binding substantially increases the binding of 36D5 to gp120 in the intact Env trimer, consi

90 Binding of these proteins to GPCRs usually requires the

91 A putative binding of ABA to GRP78, a key regulator of endoplasmic

92 Binding of BRD2 to H4Ac protects the underlying acetylat

93 f Rad51 in an HDAC4-dependent manner and the binding of Ubc9 directly to HDAC4, which led to Ubc9 ace

94 the effect of N-linked glycosylation on the binding of Herceptin to HER2 protein in breast cancer an

95 ur-SNARE complex assembly rather than direct binding of each to HOPS.

96 epsilon toxin cytotoxicity by enhancing the binding of this toxin to host cells.

97 than murine (m) PD-1 interactions, stronger binding of hPD-1 to hPD-L2 than hPD-L1, and comparable b

98 We found that the binding of Ca(2+) to hSCGN promotes the dimerization of

99 In contrast, we found that binding of TFAM to HSP and the subsequent recruitment of

100 Binding of Hic to hTSP-1 is inhibited by heparin and cho

101 Noncovalent binding of biopharmaceuticals to human serum albumin pro

102 It is not yet understood how the binding of Ca(2+) to human SCGN (hSCGN) promotes secreti

103 The binding of human IgG1 to human Fc gamma receptors (hFcga

104 Furthermore, specific binding of rhAPC to human neutrophils via VLA-3 was inhi

105 These results likely reflect insufficient binding of mAgrin to hypoglycosylated alpha-DG on muscle

106 Binding of beta-arrestin1 to IGF-1R leads to ligand-depe

107 Our data demonstrate that binding of IL-5 to IL-5Ralpha receptors enhances angioge

108 site within DARC is key to the preferential binding of DBP to immature reticulocytes, which is the p

109 Binding of this domain to Importin alpha1 (Impalpha1) wa

110 ed iNOS transcription through inhibiting the binding of Stat1 to iNOS promoter.

111 inium-labeling of AtRALF1 indicated that the binding of AtRALF1 to intact roots is CML38-dependent.

112 We examine whether binding of cytoskeletal adaptors to integrin cytoplasmic

113 lating platelet activation that involves the binding of MMP-2 to integrin alphaIIbbeta3 and the subse

114 ation at Ser-1441/1443, leading to increased binding of Rac1 to IQGAP1 and thus higher levels of cort

115 ed an off-cycle pathway involving reversible binding of molecular oxygen to iridium, which contribute

116 t mechanism do such modifications affect the binding of an IDP to its partner protein?

117 nding specificities, why lipid increases the binding of apoE to its receptor, and why specific residu

118 Binding of calcium to its intracellular receptor calmodu

119 structural and thermodynamic consequences of binding of each ligand to its allosterically coupled sit

120 Binding of IFNs to its receptors, IFNAR1 and IFNAR2, is

121 Zika infection disrupts the binding of MSI1 to its endogenous targets, thereby dereg

122 Reciprocally, the binding of nucleic acids to its N-terminal RNA recruitme

123 ion between Tug1 and PGC-1alpha promotes the binding of PGC-1alpha to its own promoter.

124 Moreover, we present evidence that the binding of DPP3 to KEAP1 stabilizes the latter.

125 is regularity is reflected in the consistent binding of dArmRP to (KR)-peptides, where affinities dep

126 Binding of Isl1/Lhx3 to later motor neuron enhancers dep

127 single domain antibody mimics the effect of binding of HIV integrase to LEDGF which is crucial for H

128 aper describes an assay that can profile the binding of a protein to ligands and can rank the affinit

129 on expression studies in cells and on direct binding of purified protein to lipids.

130 Binding of TZAP to long telomeres represents the switch

131 The binding of platelets to lymphocytes was blocked with ant

132 Thus, we speculate that if we induce the binding of platelets to lymphocytes, we will be able to

133 insic fluorescence enhancement observed upon binding of LM pectin to lysozyme was correlated with the

134 cromolecular function and drives cooperative binding of ligands to macromolecules.

135 esults (at 15-25 A resolution) indicate that binding of ATP to MalK2 promotes an asymmetric, semi-clo

136 Our data show that binding of sCD83 to MD-2 alters this signaling cascade b

137 eceptors upon ligand binding, the sequential binding of receptors to membrane coupling proteins, and

138 These results show that initial binding of organometallic compounds to MerB occurs at D9

139 The approach is used to profile the binding of chromodomain proteins to methylated lysine pe

140 Binding of peptides to MHC class I (MHC-I) molecules is

141 ylation of CRMP-2, which results in elevated binding of CRMP-2 to microtubules and a concomitant incr

142 Stability can be improved by binding of vitamin A to milk protein.

143 n the mutant CALR C terminus influences both binding of mutant CALR to MPL and activation of MPL sign

144 and its chaperone function are regulated by binding of ATP/ADP to mtHsp70's nucleotide-binding domai

145 The drug also prevented binding of recombinant DEPTOR to mTOR in the SPR assay.

146 Apparent binding of tau to MTs was similar in axons and dendrites

147 ensal Bacteroides thetaiotaomicron decreased binding of E. coli to mucin and increased the attachment

148 show in vitro and ex vivo that CotE enables binding of spores to mucus by direct interaction with mu

149 This suggested that binding of MDDEF to MVAPP is necessary to guide ATP into

150 eriments revealed that FGF13 potentiates the binding of calmodulin to NaV1.5 and that phosphomimetic

151 ow-coordinated Cu atoms and the weakening of binding of Cu to neighboring atoms help drive this proce

152 Binding of MC159 to NEMO does not disrupt the IKK comple

153 We find that binding of Gbetagamma to NF1 inhibits its ability to ina

154 t that a relatively simple mechanism for the binding of ssDNA to non-specific SSBs may be at play, wh

155 ises questions about the possible off-target binding of this tracer to non-tau molecules associated w

156 However, reduced extracellular binding of VEGF-A to Nrp1 is known to disrupt post-natal

157 Olfaction is mediated by the binding of odorant molecules to olfactory receptors (ORs

158 hether this modification is required for the binding of NS5A to other cellular proteins.

159 No binding of PTX2 to other vitamin K-dependent proteins wa

160 Here, we characterized the binding of ataxin3 to p97, showing that ataxin3 binds wi

161 We deploy this approach to show that the binding of cGMP to pacemaking ion channels is weakened b

162 of magnitude increase is due to preferential binding of PHF1 to partially unwrapped nucleosomes, and

163 cultured cells, where this GPC increased the binding of Hh to Patched 1 (Ptc1).

164 Direct high-affinity binding of hPg/plasmin to pattern D GAS is fully recapit

165 eta(2)-O2)] is attributed to the enthalpy of binding of O2 to [Pd(IPr)2] (-14.5 +/- 1.0 kcal/mol) tha

166 Binding of siRNA to PEI-polymer was characterized and co

167 The binding of PF4 to perlecan was found to inhibit both FGF

168 hibitory monoclonal antibody to CyRPA blocks binding of CyRPA to PfRh5 and complex formation thus ill

169 n thus would be favorable for the postulated binding of E7 to phosphatidylethanolamine lipid headgrou

170 The MARCKS peptides antagonize the binding of factor Xa to phosphatidylserine and inhibit t

171 t validated, nor were MFIs compared with 1:1 binding of FcMonoIgG to primary Abs.

172 t could trigger changes (for example, in the binding of microcystin to proteins).

173 layers previously oxidized, and the covalent binding of amino-oligonucleotides to pure p-MBA monolaye

174 Furthermore, dose-dependent binding of human VWF to purified recombinant human MGL w

175 We show that this is due to sustained binding of B-Raf to Rap1.

176 Plk1 phosphorylation sites in regulating the binding of FoxM1b to Rb and DNMT3b.

177 -AC), patient body motion (+MC and -MC), and binding of the tracer to red blood cells (+BB and -BB) w

178 To better understand binding of clinical inhibitors to resistant HIV-1 protea

179 nd in cultured cells by interfering with the binding of HuR to RNA.

180 study investigates how microRNAs affect the binding of proteins to RNA.

181 The binding of small ligands to RNA elements can cause subst

182 Moreover, binding of phospho-SRC1 to RORgammat displaced bound Fox

183 On the basis of the binding of PEG molecules to Rv3802, we identified its li

184 tantly, pharmacological stabilization of the binding of calstabin2 to RyR2 channels, which prevents C

185 Binding of S-peptide to S-protein results in the formati

186 Binding of miR-134 to Sabin-1 IRES caused degradation of

187 further demonstrate that MMP expression and binding of this complex to SBEs can either be enhanced b

188 We further show that binding of Plexin-B1 to Sema4A promotes the interaction

189 Actin bundling occurs due to simultaneous binding of both ABDs to separate actin filaments.

190 influencing DNA binding, actually increased binding of Dax1 to Sf1 to further enhance transcriptiona

191 ranslational support to our findings, better binding of annexin A2 to sialostatin L2 in sera from 21

192 Moreover, a predominant binding of PARP1 to single-strand DNA breaks, occluding

193 and in situ proximity analysis confirmed the binding of ACK1 to SLP-76.

194 There was increased binding of CUX1 to Snail and the E-cadherin promoter in

195 toplasmic relocalization of Cat L, decreased binding of CUX1 to Snail and the E-cadherin promoter, re

196 (APBA) to such vesicles results in specific binding of this reagent to some of the pendent cis-diol

197 In this study, we found binding of PTX3 to splenic marginal zone (MZ) B cells, a

198 study suggests the function of the membrane binding of INS is to stabilize pvLAAD structure and incr

199 tween Vn and lipid membranes, which leads to binding of autoinhibited Vn to supported lipid bilayers,

200 Binding of STIM1 to SUR1 was enhanced by poly-lysine.

201 Importantly, direct biotin-mediated binding of bacteria to surface lipids in the plasma memb

202 Direct binding of PrxII to tankyrase ARC4/5 domains seems to be

203 noprecipitation analyses reveal constitutive binding of CREB to target gene promoters in the absence

204 In this study, we characterize the binding of actoxumab to TcdA and examine its mechanism o

205 a quiescent state in CRC cells by disrupting binding of beta-catenin to TCF1 and TCF3 and regulation

206 ty acids was found to play a key role in the binding of a glycolipid to the carbohydrate recognition

207 ting RNA editing, as evidenced by the direct binding of ADAR3 to the GRIA2 pre-mRNA.

208 The binding of ALO-D4 to the plasma membrane was virtually e

209 the role played by Ca(2+) in the reversible binding of annexin to the membrane surface.

210 B-cell activation is initiated by the binding of antigen to the B-cell receptor (BCR).

211 tion of TFPI-2 with Ap-2alpha attenuated the binding of AP-2alpha to the MMP-2 promoter, therefore re

212 ChIP experiments revealed a preferential binding of BRD4 to the Myog promoter during C2C12 myobla

213 e membranes; and (v) phosphorylation-induced binding of cdb3-PO4 to the membrane-spanning domain of b

214 sly described auto-inhibition mechanism, the binding of Chp2 to the H3K9me3 mark is not analogously r

215 phosphorylation of certain residues impaired binding of chromodomains to the peptide ligands.

216 hat neuronal activity induces a preferential binding of CRTC1 to the transcriptional complex in CRE/T

217 ferred route begins with a bidentate chelate binding of deprotonated substrate to the Ni.

218 eristics of hemoglobin (Hb) changes with the binding of dioxygen (O2) to the heme prosthetic groups o

219 monstrated by genome-wide RNA-seq and direct binding of Dmrta2 to the Hes1 genomic locus.

220 We propose that, in this case, binding of DNA to the second site is precluded and modul

221 Lastly, we show that the binding of dynein to the microtubule is associated with

222 The cross-reactive VHHs block binding of EF/LF to the protective antigen C-terminal bi

223 protein synthesis typically begins with the binding of eIF4F to the 7-methylguanylate (m(7)G) cap fo

224 y, we found that cAMP elevation caused rapid binding of Epac2A to the beta-cell plasma membrane, wher

225 and absorption studies support the multiple binding of F-groups to the C-center of CO2 (CF 3.190(9)-

226 Blockade of alphavbeta1 prevented direct binding of fibroblasts to the latency-associated peptide

227 Binding of FK506 to the FKBP domain causes the target do

228 ults, at least in part, from higher-affinity binding of Fur to the "late"-induced genes.

229 Binding of gp120 to the receptor, CD4, changes the Env c

230 Binding of H3K4me3 to the RAG-2 PHD induces conformation

231 The BabA adhesin mediates high-affinity binding of Helicobacter pylori to the ABO blood group an

232 ich were found to bind IL-15, to inhibit the binding of IL-15 to the IL-2Rbeta chain or the prolifera

233 Binding of IL-33 to the IL-33R induces activation of the

234 ine at position 135 completely abolished the binding of LPS to the hMD-2 mutant.

235 iquitination by MDM2, a process initiated by binding of MDM2 to the intrinsically disordered transact

236 tinct domains designated S1(A) through S1(D) Binding of MERS-CoV to the cell surface entry receptor d

237 ence of the fluoroionophore is enhanced upon binding of Na(+)-ions to the highly selective aza-crown

238 The binding of NAD(+) to the NHD domain of DBC1 (deleted in

239 le and this presentation could influence the binding of neutralizing antibodies to the virus.

240 e transcription factor NF-kappaB and enhance binding of NF-kappaB to the IFNG genomic locus.

241 ch-Rheb regulatory loop, in which the cyclic binding of Notch1 to the Notch-responsive elements (NREs

242 obably because these mutations decreased the binding of NS1 to the cleavage and polyadenylation speci

243 ChIp analyses indicated the binding of p53 to the promoter region of miR-199a-3p.

244 rther showed that the sdAb-Fcs do not affect binding of PCSK9 to the LDLR but rather block its induce

245 proteinuria through cGMP- and PKG-dependent binding of PPAR-gamma to the TRPC6 promoter, which inhib

246 Similarly, binding of properdin to the surface of human umbilical v

247 mines the initial crosslinking of cisplatin, binding of proteins to the genome largely contributes to

248 d in this species, possibly due to a favored binding of Pt to the polysaccharide-rich cell wall of th

249 promotes phosphorylation of Pxn and Pyk2 and binding of Pxn to the alphaE/CD103 subunit tail.

250 Tgf-beta) decreased Satb1 expression through binding of Smad proteins to the Satb1 promoter.

251 The binding of small molecules to the thyroxin-binding sites

252 with BRG1 in differentiating melanocytes and binding of SOX10 to the Tyrp1 distal enhancer temporally

253 ty protein 1 (Sp1), which then inhibited the binding of Sp1 to the VEGF promoter to reduce VEGF expre

254 chanistic model in the field postulates that binding of ssDNA to the OB core induces the flexible, un

255 firmed that Lyn overexpression decreased the binding of STAT6 to the promoter region of Muc5ac in mic

256 coimmunoprecipitation indicated differential binding of Syncrip to the long versus short 3'UTR.

257 Binding of TcdA to the host cell surface was directly bl

258 We find that binding of TDP-43 to the translational machinery is medi

259 Binding of TEFM to the DNA forms a downstream "sliding c

260 these data suggested that the expression and binding of TFs contributed to the establishment of subse

261 he experiments and shows preferential strong binding of the AFP to the fast growing surfaces of the s

262 These actions result from the specific binding of the antibody to the beta-subunit of Fsh to bl

263 Binding of the capsid to the nuclear pore complex (NPC)

264 This effect is related to a favorable binding of the comonomer to the active site comprising c

265 eparation effectively prevents the potential binding of the counteranion to the cationic metal center

266 osphorylation weakens this stabilization and binding of the heads to the backbone.

267 fected cell lines that were unrelated to the binding of the MAb to the target cells.

268 8], which we find additionally required for binding of the MCC to the APC/C and for MCC disassembly.

269 d as a fusion to the relevant enzyme so that binding of the receptor to the immobilized ligand brings

270 otein receptor brings about the strong total binding of the toxin to the neuronal membrane.

271 It allows binding of the tRNAs to the ribosomal A and P sites, but

272 Transactivation is mediated by direct binding of TSARs to the N-box in the promoter of HMGR1.

273 ear magnetic resonance demonstrated specific binding of UM101 to the computer-aided drug design-targe

274 Annexin A2 facilitates the binding of Vamp8 to the autophagosomal SNARE Syntaxin 17

275 ion has previously been shown to inhibit the binding of VWF to the platelet surface receptor glycopro

276 We demonstrate the direct binding of VX-809 to the first nucleotide-binding domain

277 This pathway is initiated by the binding of Wnt ligands to the Frizzled receptor, the ass

278 Interestingly, the binding of YscP to the slowly self-cleaving YscU variant

279 Binding of chemokines to their cognate receptors on mono

280 was transcriptionally upregulated by direct binding of HOXA5 to their promoter sequences as demonstr

281 in the cell relies on the rapid and specific binding of molecules to their cognate targets.

282 inding site enrichment analysis verified the binding of these MRs to their predicted targets.

283 Binding of FACT to these genomic regions triggers a p53

284 from an axonal injury express uPAR and that binding of uPA to this uPAR promotes axonal recovery by

285 Binding of MfP to Toll-like receptor 4 (TLR4) was determ

286 leukemic cell differentiation revealed that binding of S100A9 to Toll-like receptor 4 (TLR4) promote

287 the capsid (Gly299Lys/Ala300Lys) altered the binding of the capsid to transferrin receptor type 1 (Tf

288 Binding of Lin28a to TRBP in vitro is also enhanced by p

289 ease of intracellular calcium concentration, binding of calcium to troponin in the actin-containing t

290 Vinblastine inhibited the binding of crocin to tubulin while podophyllotoxin did n

291 ha electrostatically repels the DNA, and the binding of IkappaBalpha appears to twist the NFkappaB he

292 Our data also reveal a binding of up to two Ca(2+) ions to C9.

293 the Tup-family corepressors) suppress direct binding of Rst2 to UAS2, but this suppression is counter

294 ve mass spectra matching, the promiscuity of binding of cisplatin to ubiquitin is revealed, with 14 d

295 Binding of UBA5 to UFM1 is mediated via an amino acid se

296 onal studies have provided insights into the binding of ERCC1-XPF to various DNA substrates.

297 We observe that binding of agonists to VFD2 of TAS1R2 leads to major con

298 ol 3-kinase VPS34 activity by increasing the binding of phosphatidylinositol to VPS34.

299 mics simulations to investigate the specific binding of cardiolipins to yAAC3.

300 Here the binding of pyridyl ligands to zinc porphyrins with thioe