ライフサイエンスコーパス: be bound to

1 resent on the receptor itself or a ligand it is bound to.

2 emain spatially confined on the surface they were bound to.

3 faster electron injection dynamics when MK-2 is bound to {010} compared to other facets, consistent w

4 in anti-gD monoclonal antibodies (MAbs) that are bound to a biosensor chip, (ii) gD is bound to eithe

5 Ezh2, Eed, and the VEFS domain of Suz12 and are bound to a cancer-associated inhibiting H3K27M pepti

6 formed from heterometallic {Cr(7)Ni} rings, are bound to a fluoride-centered {CrNi(2)} triangle.

7 igh-specific-activity radiolabeled mAbs that are bound to a tumor surface will penetrate slowly compa

8 results confirm that phenolics studied here are bounded to a membrane surface predominantly via hydr

9 he N-terminus of the amphipathic alpha-helix is bound to a cleft in the regulatory domain, leading to

10 lectively associating with Hsp70 after Hsp70 is bound to a client protein.

11 We show that purified AerR contains B12 that is bound to a conserved histidine (His145) in AerR.

12 Cationic gold complexes in which gold is bound to a formally divalent carbon atom, typically f

13 as H2 Pt(HCO2 )(-) , where the platinum atom is bound to a formate moiety on one side and two hydroge

14 the conformational shift observed when RhoA is bound to a guanine nucleotide exchange factor.

15 the fraction of an epigenetic modifier that is bound to a pharmacological inhibitor (target engageme

16 The receptor is bound to a positive allosteric modulator 'megabody' a

17 Thiophosphate is bound to a site in the alpha(E)beta(E)-catalytic inte

18 f tumor-prone keratinocytes, and each factor is bound to a specific promoter region featuring an NF-k

19 These analyses revealed that PDC-E2 is bound to a STAT5-binding site in the promoter of the

20 nriched alkylboronate esters, in which boron is bound to a stereogenic carbon, and we highlight the u

21 When the U2AF heterodimer is bound to a strong, uridine-rich splice site, U2AF2 sw

22 y coordination complexes in which dihydrogen is bound to a subvalent transition metal center.

23 of parameters of the thrust, the spacecraft is bounded to a given altitude.

24 hydrogens of BCA was higher when the protein was bound to a ligand with five glycine subunits than wh

25 First, a protein molecule was bound to a linker in the bulk solution and then this

26 nd to a polycarbonate membrane, which itself was bound to a molecular mechanics chamber.

27 filaments moved processively on F-actin that was bound to a PEG brush surface.

28 The PDMS chamber was bound to a polycarbonate membrane, which itself was

29 We showed that most ES-62 was bound to a single protein, C-reactive protein (CRP),

30 A minimal actin cortex was bound to a supported lipid bilayer via biotinylated

31 Only when D403E Pol III was bound to a tau-containing DnaX complex did exchange

32 First, silica nanoparticles (NPs) were bound to a hydrophobic micro-sized polymer containi

33 rated, are significantly reduced when Cu(2+) is bound to Abeta or alphaS, particularly when they are

34 These studies indicated that (i) EGCG was bound to Abeta monomers and dimers, generating more

35 When Myo51-Rng8/9 was bound to actin-tropomyosin, two attachment sites wer

36 sue-specific coding and non-coding RNAs that are bound to active promoters and enhancers, especially

37 Mechanistically, we show that ASK1 is bound to active IGF1R and inhibited by Tyr and Ser83/

38 nd that a significant portion of nuclear FUS was bound to active chromatin and that the ALS mutations

39 articles (A-3',4'-OH-TPN2), in which PEG2000 was bound to adenosine on the 3',4' hydroxyl groups, sti

40 G400-N(3) and PLA-b-PEG2000 block copolymers were bound to adenosine at the 3',4'-OH, 5'-OH, and 6-NH

41 the hinge region of soluble IgG and when IgG is bound to Ag, resulting in one F(ab')2 molecule and on

42 They are bound to airborne particles and transported over lon

43 Here we show that dissolved U(VI) can be bound to amorphous iron phosphate during their deposi

44 in the maximal absorbance wavelength when CR is bound to amyloids.

45 when proteins, such as CRE-binding protein, are bound to an adjacent cis-regulatory element.

46 T cells indirectly sense self antigens that are bound to an antigen-presenting molecule.

47 e fluorescence is efficiently quenched by it being bound to an activatable trigger group through a no

48 und APO form and a HOLO form (where the PDZ1 is bound to an 11-residue peptide derived from the C ter

49 and an active form in which the heterodimer is bound to an agonist and a positive allosteric modulat

50 here that when a Au25(SG)18 metallic cluster is bound to an alpha-hemolysin (alphaHL) nanopore, the m

51 In the active state, the BBSome is bound to an Arf-family GTPase (ARL6/BBS3) that recrui

52 f the oxaloacetate and acetyl-CoA substrates is bound to an independent site near the metal coordinat

53 The anti-8OHdG was bound to an amine modified gold support through its

54 e voltage-gated sodium channels (Nav), which are bound to ankyrin particles, a critical axonal protei

55 hnRNP K protein was bound to antioxidant NFE2L2 transcripts encoding Nrf

56 Although the majority of plasma S1P is bound to apolipoprotein M (ApoM) in the high-density

57 Mutant ER was bound to approximately a quarter of mutant-enriched

58 SLIRP was bound to ARE's of AR target genes in the absence of

59 However, when AAA4 is bound to ATP, the gating of AAA1 by AAA3 prevails and

60 elf-interaction in isolated Int and when Int is bound to attachment sites.

61 ictates that the absorptivity and emissivity are bound to be equal in reciprocal systems at equilibri

62 st decade, and many exciting new discoveries are bound to be made in the coming years that will expan

63 eased by an order of magnitude when cadherin is bound to beta-catenin.

64 (alpha-Lac), and bovine serum albumin (BSA) were bound to beta-C with overall binding constant value

65 The purified CD200-SA protein was bound to biotin-coated fluorescent polystyrene parti

66 in the Western Antarctic Peninsula sediments were bound to black carbon or recalcitrant tar-like orga

67 inal domain, is observed only when ATPgammaS is bound to both the D1 and D2 domains of the protomer.

68 Calcium was bound to both the transmembrane component and the he

69 the cytoplasmic calcium in cardiac myocytes is bound to buffers, and their properties will therefore

70 However, when PLCbeta is bound to C3PO, the hydrolysis rate of siRNA(GAPDH) be

71 h the unique Fe atom of the [4Fe-4S] cluster is bound to C5' of the 5'-deoxyadenosyl radical (5'-dAdo

72 reen to red fluorescence if, and only if, it is bound to calcium.

73 nal epitope on CD81 that is masked when CD81 is bound to CD19.

74 When CpdR is unphosphorylated and when PopA is bound to cdG, they work together with RcdA in an all-

75 les functionalized with short-chain peptides are bound to cells through antibody-antigen interactions

76 re and thus the climate, the microbial world is bound to change and adapt as well.

77 Vanillin and trans-cinnamaldehyde were bound to chitosan by Schiff base reaction and reduc

78 nomic profiling strategy in which antibodies are bound to chromatin proteins in situ in permeabilized

79 Neither mcd1-1p nor smc3-42p is bound to chromosomes when expressed individually at i

80 We argue that such bottom-up proposal is bound to commit a mistake of reification: It treats t

81 n Abeta(1-42) aggregates, including fibrils, are bound to Cu(II) ions, they retain their redox activi

82 exes, ACD6 forms soluble complexes, where it is bound to cytosolic HSP70, ubiquitinated, and degraded

83 ence presented here, in which the ASncmtRNAs are bound to Dicer and knockdown of the ASncmtRNAs reduc

84 Heterogeneous glycans may be bound to different amino acid residues, forming multi

85 CoA thioesterase activity, reveals that CoA is bound to different parts of the core domain in these

86 suggests that (i) short-residence molecules are bound to DNA non-specifically, and (ii) that non-spe

87 h disparities in proliferative response, Myc is bound to DNA at open elements in responsive (liver) a

88 aced to a non-inhibitory position, when ETV6 is bound to DNA containing a consensus (5')GGAA(3') reco

89 ne burst as long as the transcription factor is bound to DNA, and bursts terminate upon transcription

90 elomere repeat binding factor (hTRF1), which is bound to DnaK in a globally unfolded conformation.

91 chemical studies demonstrated that NKG2D(TR) was bound to DNAX-activated protein of 10 kDa (DAP10) an

92 Two interacting BaPif1 molecules are bound to each fork of the partially unwound dsDNA, a

93 monolayer, but an assembly of proteins that are bound to each other.

94 odimer at the center, and two alpha-subunits are bound to each side of the beta(2) dimer, creating an

95 und that only a single antibody molecule can be bound to each prM protein at any given time.

96 Unexpectedly, a lipid ligand is bound to each 3HB6H monomer.

97 One IsdH molecule is bound to each alpha and beta Hb subunit, suggesting t

98 el discovery that in resting cells myoferlin was bound to EHD2 protein and when cells were treated wi

99 with nucleotide occupancy: five MCM subunits are bound to either ATPgammaS or ADP, whereas the apo MC

100 f Isw1 docks at the SHL2 position when ISW1a is bound to either mono- or di-nucleosomes, there are ma

101 lving a different degree of bending when DNA is bound to either MutSalpha or MutSbeta and a more like

102 that are bound to a biosensor chip, (ii) gD is bound to either one of its receptors on a chip, and (

103 rein-high molecular weight kininogen complex is bound to endothelial cells, prekallikrein is stoichio

104 Furthermore, we observe that p53 is bound to enhancer elements in healthy fibroblasts and

105 ion networks, functional clustering of genes is bound to evolve during neurodevelopment and disruptio

106 olic product of cell membrane sphingolipids, is bound to extracellular chaperones, is enriched in cir

107 estigations revealed that 16:0 acylcarnitine was bound to factor Xa and that binding did not require

108 h negligible degradation of iC3b by hPm that is bound to fibrinogen on the cells.

109 N, yet Avastin could still bind to VEGF that was bound to FN, indicating that these binding events ar

110 l region within SSB is observed only when it is bound to forked structures.

111 When CaM is bound to full-length RyR1, either purified or in SR m

112 m(-1) s(-1)) was decreased ~10-fold when FXa was bound to FVa in prothrombinase and a further ~3-4-fo

113 ydrogen bonds that gets disrupted when Cdc42 is bound to GDP, a disruption that does not exist in oth

114 oved away from some of the binding sites and was bound to GLIC asymmetrically at the end of simulatio

115 ycans in the skin interstitium, where sodium is bound to glycosaminoglycans without commensurate effe

116 presentation complexes, is impaired when CD4 is bound to gp120.

117 The LPL within capillaries is bound to GPIHBP1, an endothelial cell protein with a

118 ue, among other causes, to proanthocyanidins being bound to grape cell wall polysaccharides, which ar

119 Physiologically, CaM is bound to >70% of RyR2 monomers and inhibits sarcoplas

120 iphosphate, activating Ras into inactive Ras is bound to guanosine diphosphate, inactivating Ras.

121 s Ras/ERK signaling by converting active Ras is bound to guanosine triphosphate, activating Ras into

122 differentiation genes, including involucrin, are bound to heavy polysomes during differentiation, des

123 -disrupting peptide that is inactive when VI is bound to hexon trimers.

124 double resonance showed that the Mn(II) ions are bound to histidines and phosphate groups, mostly fro

125 We also demonstrate that Rad51 is bound to HPV31 genomes, with binding increasing per v

126 ates where an acid is ionized in BR, a Cl(-) is bound to HR in a position near the deleted acid.

127 containing adenine and uridine-rich elements were bound to ILF3 through RNA immunoprecipitation.

128 nding studies showed that purified factor Xa was bound to immobilized peptides HC796-835 and HC816-83

129 erived from the human immunodeficiency virus was bound to immunogenic liposomes for potent antibody g

130 The H1.0 globular domain is bound to Impbeta, whereas the acidic loops of Impbeta

131 ata demonstrate that the maize CFM1 ortholog is bound to introns whose splicing is disrupted in the c

132 geared toward restricting Bok to that which is bound to IP3Rs, implies that unbound Bok is deleterio

133 nking dynactin to dynein only when the motor is bound to its proper cargo.

134 ide that adopted an alpha-helical dimer, and was bound to K2hPg with nearly the same affinity as PAM

135 come available when KCNE1 accessory subunits are bound to Kv7.1 channels.

136 oving alone, as part of a larger complex, or are bound to large cellular components such as the membr

137 In human plasma, 30-40% of PCSK9 is bound to LDL particles; however, the physiological si

138 in Criteria [RDoC] framework, in particular) are bound to lead to eliminativism rather than reduction

139 surface is normally covered with sugars that are bound to lipids or proteins.

140 In MagPIE, synthesized DNA is bound to magnetic beads, which are then incubated wit

141 links immunoglobulin E (IgE) antibodies that are bound to mast cells and basophils, triggering the re

142 creased in response to extracellular Ca(2+), was bound to mechanistic target of rapamycin (mTOR) comp

143 t peptides to this optimal length while they are bound to MHC I molecules (using the latter as a patt

144 ion, the peptide portion of the glycopeptide is bound to MHCII, allowing the covalently linked glycan

145 e myristoyl group is readily exposed when MA is bound to micelles or bicelles.

146 ubule-binding sites remain flexible when Tau is bound to microtubules in agreement with a highly dyna

147 There was a reduction in oxidation when iron was 'bound' to milk or peptides compared to free ferrous

148 -driven transformations when these compounds are bound to mineral surfaces, and how their transport i

149 r two different miRNAs or when the two sites were bound to miRNAs loaded into two different AGO paral

150 Unexpectedly, two phospholipids are bound to MlaFEDB, suggesting that multiple lipid sub

151 y translocated to the mitochondria, where it is bound to mtHtt in various HD models.

152 e address the mechanism of sorting when FcRn is bound to multivalent IgG-opsonized antigens.

153 This suggests that many types of ligands can be bound to nanoparticles, preserving ligand and nanopar

154 His-tagged galectin-3 was bound to nickel chelate acceptor beads, whereas biot

155 C3, C4, and C1q are bound to NKAP-deficient peripheral T cells, demonstr

156 (XAS) analysis of the peat confirmed that As was bound to NOM thiol groups and incorporated into pyri

157 s study, we demonstrate that PRRSV N protein is bound to Nsp9 by protein-protein interaction and that

158 r 2 (TLR2) activation, and this whether they are bound to nucleic acids or not.

159 their substrates most efficiently when both are bound to nucleic acids.

160 anscripts accumulate in nuclear speckles and are bound to Nxf1.

161 Most of the water molecules are bound to OH groups even at the highest hydration lev

162 In SIgA, SC is bound to one face, asymmetrically contacting both IgA

163 end of the phi812 double-stranded DNA genome is bound to one protein subunit from a connector complex

164 p53 DNA REs suggesting that one p53 tetramer is bound to one RE.

165 ies showed that the full-length p53 tetramer is bound to only one half-site of RE.Here, we have used

166 th PhIL1 were identified, showing that PhIL1 was bound to only some proteins present in the glideosom

167 that Bak is activated and that activated Bak is bound to p53 during reovirus encephalitis.

168 When Abs that are bound to pathogens enter the cell as immune complexe

169 cles in which the cytosolic tail of rOATP1A1 is bound to PDZK1.

170 of the pathobiont Streptococcus pneumoniae, is bound to peptidoglycan (wall teichoic acid, WTA) or t

171 experiments with cell lines, in vivo, Zap70 is bound to phosphorylated ITAMs in resting T cells.

172 ine the structure of PsbP and PsbQ when they are bound to Photosystem II.

173 Moreover, SRSF5 is bound to pluripotency-specific transcripts such as Li

174 o azide groups ensures that all Cu catalysts are bound to polytriazole polymers at low monomer conver

175 Furthermore, we show that MglA-SspA must be bound to ppGpp to mediate high-affinity interactions

176 previous studies showed that Hdac1 and Hdac2 are bound to promoters of key renal developmental regula

177 We further show that ARID1A is bound to promoters with open chromatin, but ARID1A lo

178 a significant fraction of intracellular cAMP is bound to protein in mycobacterial species, and by usi

179 We show here that CP33B is bound to psbA mRNA in vivo, as was shown previously f

180 lative SEM and nanoSIMS) that organic carbon is bound to reactive Fe primarily in the transition betw

181 aptation to conditions within the human host is bound to reveal novel strategies and targets for ther

182 Specifically, 535 nm-emitting CdTe QD were bound to Rhodamine B (RB) through the peptide for i

183 l esters stored in lipid droplets when ORP1L was bound to RIDalpha.

184 ge fraction of the spermine present in cells is bound to RNA but apparently does not condense it.

185 of RfaH refolds from an alpha-hairpin, which is bound to RNA polymerase binding site within the N-ter

186 Our results show that when NP is bound to RNA, the protein is highly dynamic and the s

187 en proposed previously, poliovirus RdRp that was bound to RNA with an incorporated 2'-C-methyl nucleo

188 was unreactive towards TTP when the protein was bound to RNA, thus suggesting a protective effect of

189 nes, and show that 96% of proteins recovered were bound to RNA.

190 -FRET to assess interlobe distances when CaM is bound to RyR1 in SR membranes, purified RyR1, or a pe

191 (+) In addition, our data suggest that Cl(-) is bound to SERT during the entire catalytic cycle.

192 ve in Siberia contribute to the decline that is bound to show catastrophic consequences very soon.

193 ive to reaction with O(2) and NO when SvWhiD was bound to sigma(HrdB) (4), consistent with protection

194 MTM SA-Phe is bound to sites AGGG and GGGT on one DNA, and to AGGG

195 The MLF complex is bound to sites of nucleosome depletion and sites cont

196 nally, these unique structural conformations are bound to small molecule ligand libraries to predict

197 More Pu(IV) than (V) was bound to soil colloidal organic matter (COM).

198 Antibody-functionalized magnetic beads were bound to specific antigens expressed on the target

199 SF), a galectin-3 nanomolar binding partner, was bound to streptavidin-coated donor beads.

200 ctivated conformation (CB2(SH3/W24A-E262A)), were bound to supported membranes in the absence or pres

201 When Cy5-labeled Escherichia coli (Ec) SSB is bound to surface-immobilized 3'-Cy3-labeled ssDNA, a

202 e from C. thermarum, ATP and a magnesium ion are bound to the alpha-helices in the down state.

203 evealed that all four Ag(+) ions of Ag(4)-MT are bound to the beta-domain.

204 s, which via biotin-streptavidin interaction are bound to the biotinylated surface of the target cell

205 noRNPs, subtly different in how the proteins are bound to the C/D motif, leading to 2-O-methylation o

206 In 3D-MTC, ferromagnetic beads are bound to the cell surface via surface receptors, fol

207 substrate Gad8 are found in the nucleus and are bound to the chromatin.

208 and reverse genetics that these RNA segments are bound to the coat proteins in a sequence-specific ma

209 ipid kinase PIKFYVE and the phosphatase FIG4 are bound to the dimeric scaffold protein VAC14, which i

210 owed that both E- and D-domain of fibrinogen are bound to the EMT zeolite NPs via strong electrostati

211 l adherence is opposed by TG2 molecules that are bound to the endothelial surface.

212 and mouse models, most VEGF165a and VEGF165b are bound to the extracellular matrix.

213 When oxidatively stable chelate ligands are bound to the iridium in addition to the Cp*, the oxi

214 and thinking science are not activities that are bound to the laboratory.

215 on is first used to enrich for proteins that are bound to the ligase trap.

216 when rolling circle amplified DNA molecules are bound to the magnetic nanobeads.

217 Whereas the halide/pseudohalide anions are bound to the metal centers and thus stationary, the

218 achieve insufficient removal of metals that are bound to the organic fraction of the sludge.

219 ic reagents (typically water-insoluble) that are bound to the paper, thus not subject to being washed

220 We discuss how these c-di-AMP molecules are bound to the protein and riboswitch receptors and wh

221 e structural analysis showed that the sugars are bound to the protein mainly by hydrogen bonds, and t

222 gnificantly decreased when the two rexinoids are bound to the receptor.

223 Importantly, these inter-Landau-level states are bound to the topological singularity and have energi

224 concentration, which means if all inhibitors are bound to the virus.

225 excess Ag(+) ions, and these are assumed to be bound to the alpha-domain or shared between the two d

226 formed, indicating that both substrates must be bound to the enzyme for the reaction to proceed.

227 g to the heavy chain required that MTIP also be bound to the heavy chain, unlike MTIP that bound the

228 bR and RegA proteins interact, but CbbR must be bound to the promoter DNA in order for RegA-CbbR prot

229 antigens are capable of reusing MR1 that had been bound to the folic acid metabolite 6-formylpterin (

230 -enzyme intermediate revealed that avibactam is bound to the active-site serine in two orientations ~

231 appear to have little effect on Capu once it is bound to the barbed end of an elongating filament.

232 nteractions with the cosubstrate, SAM, which is bound to the catalytic iron-sulfur cluster.

233 TIMP-3 inhibits ADAM17 activity only when it is bound to the cell surface and that cell surface level

234 However, when AlfB is bound to the centromeric DNA sequence, parN, it forms

235 3gamma2L GABA(A) receptor in lipid nanodiscs is bound to the channel-blocker picrotoxin, the competit

236 the paralog CRY2 and reduced when either CRY is bound to the circadian corepressor PERIOD2.

237 drogen bonds with one such water (W1), which is bound to the dangler Mn4A of the oxygen-evolving comp

238 via Ku70/80 and is activated once the kinase is bound to the DSB ends.

239 (which are six coordinate when only alphaKG is bound to the Fe(II)), alphaKG binding to Fe(II)-DAOCS

240 WAC is bound to the Golgi by GM130.

241 ctive genes: In undifferentiated cells, PBX1 is bound to the H1-compacted promoter/proximal enhancer

242 ring disk electrochemistry), when imidazole is bound to the heme (Fe(Im)Cu), this same selective O2-

243 dinitrosyl complexes, where one NO molecule is bound to the heme iron to form a five-coordinate low-

244 tate of the catalytic cycle-when Fe(3+)-heme is bound to the HRMs and the core is in the apo state.

245 ace water diffusion, i.e., how tightly water is bound to the hydrophilic surface and surrounding wate

246 ron diffraction experiments indicate that NO is bound to the iron centers of the framework with an Fe

247 T7A1, we conclude that downstream duplex DNA is bound to the jaw in an assembly with SI3, and bases -

248 NusA, functions as an antiterminator when it is bound to the lambdoid phage derived antiterminator pr

249 udies have identified an adduct in which CO2 is bound to the ligand and metal, [((t)Bu-PNP-COO)Ir(H)2

250 ndicate that a highly distorted CO2 molecule is bound to the metal center in an eta(2)-C,O coordinati

251 ](+) points to a covalent structure where Pt is bound to the N7 atom of guanine.

252 22 and 1660 cm(-1), and a second NO molecule is bound to the nonheme Fe(B) site with a nu(NO)(FeB) at

253 e (SB) through which the retinyl chromophore is bound to the opsin protein.

254 We show that DNMT1 is bound to the p53 regulatory region and that loss of D

255 e structural studies demonstrate that hSpt2C is bound to the periphery of the H3/H4 tetramer, mimicki

256 Then this b-e-g-f complex is bound to the preformed F(1)-c(8) module by subunits O

257 nockout mice and that, in normal tongue, WT1 is bound to the promoter regions of these genes.

258 PKL is bound to the promoters of MIR156A/MIR156C, where it p

259 Moreover, hepatic RARbeta is bound to the putative RAREs of the Fgf21 promoter in

260 When the pan-agonist 9-cis-retinoic acid is bound to the receptor, only the dynamics of helices 3

261 unclear whether synthesis occurs while RelA is bound to the ribosome or free in the cytoplasm.

262 n is substantially decreased when the ligand is bound to the RNA, resulting in a preferential stabili

263 vators, activate Arp2/3 complex only once it is bound to the side of an actin filament [5, 6].

264 The LXRalpha-C/EBPbeta complex is bound to the SREBP-1c promoter in the absence or pres

265 ext-generation sequencing, we show that ATF3 is bound to the transcriptional regulatory regions of >3

266 increased membrane undulations when alphaSyn is bound to the vesicle's outer leaflet at a 200:1 L/P.

267 thione at the C7-C8 olefin, and this complex was bound to the active site of GSTP1; no covalent bond

268 When TNT was bound to the anti-TNT scFv-functionalized diatom fru

269 MafA was bound to the approximately 1.5 MDa Mll3 and Mll4 com

270 the heavy chain constant region, while zinc was bound to the heavy chain constant region and iron wa

271 l phase reciprocally shortened as more hemin was bound to the insoluble matrix of WCM.

272 Selenite was bound to the material via inner-sphere complexation

273 Furthermore, LPL that was bound to the N-terminal domain interacted with lipop

274 Docking results revealed beta-C was bound to the subdomain IIA of BSA, the residues of a

275 the low molecular weight compound diclofenac was bound to the surface to be used as model ligand for

276 alysis suggested that daidzein and genistein were bound to the 7S and 11S proteins.

277 alpha7 receptors activated by ACh when PAMs were bound to the allosteric binding site in the transme

278 In addition, wild-type (wt) capsids that were bound to the conformational antibody A20, which is

279 f bile salts, some released peptide monomers were bound to the micellar surface.

280 In addition, HDAC1/2 were bound to the P0 promoter and activated P0 transcrip

281 VSFS revealed that Zn(2+) and Ca(2+) were bound to the phosphate and carboxylate moieties on

282 s confirmed that both endogenous Sp1 and Sp3 were bound to the proximal promoter region of E1b.

283 Of the three transcription factors that were bound to the RhBG promoter in response to ethanol a

284 Both forms of A17 were bound to the virion membrane and associated with D1

285 S), which recognize cytokines only when they are bound to their cell surface receptors.

286 ce of magnetic fields, the charged particles are bound to their cyclotron orbits, while the neutral e

287 of these genes and confirmed that Integrator is bound to their 5' ends and negatively regulates their

288 pillary, thereby releasing the peptides that were bound to these micelles, facilitating peptide reten

289 We also found that HDAC1 is bound to this region as part of the NF-kappaBp50-HDAC

290 contrast, in venous endothelial cells, NR2F2 was bound to this site, together with ERG, and prevented

291 [1.3{CB[7]}]Cl3) in which three arms of 1Cl3 are bound to three host molecules.

292 tion (state 2) to a conformation in which it is bound to three CD4 receptor molecules (state 3)(8-10)

293 e active site of PP1cbeta is blocked when it is bound to TIMAP.

294 At higher length scales, however, we are bound to top-down nanotechnology techniques to reali

295 of an anti-termination complex in which TEFM is bound to transcribing mtRNAP.

296 ogies, and future clinical applications that are bound to transform cancer medicine.

297 Ssb is bound to translating ribosomes via ribosome-associate

298 that listerin and NEMF, core RQC components, are bound to translocon-engaged 60S subunits on native E

299 Antennas, from radiofrequencies to optics, are bound to transmit and receive signals equally well f

300 They have been found to be bound to various carriers like proteins, lipoprotein