ライフサイエンスコーパス: be bound to

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

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

3 noprecipitation revealed that RNA polymerase was bound to 70% of the TSSs, and two-thirds of these TS

4 When apo-EF-G is bound to 70S ribosomes and GTP is added, substantial

5 When EF-G-GTP is bound to 70S ribosomes, bases A1492 and A1493 are imm

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

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 To perform its function, Ras has to be bound to a membrane by a posttranslationally attached

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

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

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

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

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

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

20 ve to the DNA and to each other when SNAP190 is bound to a U1 promoter as a subunit of SNAPc.

21 Molybdenum is bound to a unique pterin, thus forming the molybdenum

22 tivated receptor-gamma LBD, in which the H12 was bound to a fluorescent probe, were performed.

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

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

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

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

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

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

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

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

31 When Hirudin(54-65) was bound to ABE I, it was still possible to bind GpIbal

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

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

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

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

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

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

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

39 N(6)-ethenoadenine and 3,N(4)-ethenocytosine are bound to AlkB more favorably in their protonated cat

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

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

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

43 We also examined whether PcG proteins are bound to an engrailed PRE in cells where engrailed i

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

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

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

47 This copper is bound to an anionic fluorescent molecule known as the

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

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

50 results revealing that one protein G in two was bound to an antibody.

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

52 ng interactions in which the extended N-lobe is bound to another CaM-binding domain.

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

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

55 ADCC, even when IdeS was added after NMO-IgG was bound to AQP4.

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

57 tly with K63-linked ubiquitin chains when it is bound to Axin in unstimulated HEK293 cells.

58 with Lys-63-linked ubiquitin chains when it is bound to Axin, but it is unclear whether this modific

59 hich the majority of the immobilized ligands are bound to BCA.

60 tive Bax localized to mitochondria, where it was bound to Bcl-xL.

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 However, such an advantage is bound to be short-lived as opposing strategies evolve

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

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

66 BE bound to bone slices and inhibited bone resorption by

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 h C3d ligands in many orientations when TT30 is bound to C3b.

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

71 lex with skeletal troponin I but not when it is bound to cardiac troponin I.

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

73 FOXM1 is bound to cell cycle-regulated genes with peak express

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

75 M, encodes two protein isoforms: SCML2A that is bound to chromatin and SCML2B that is predominantly n

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

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

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

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

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

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

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

83 No clear pattern of how strongly PAHs were bound to different biochars was found based on the

84 s the rearrangement of the enol-carbene that is bound to dirhodium to produce a donor-acceptor cyclop

85 However, only Cu and Mn were found to be bound to dissolved proteins of higher Ips in deep sea

86 In Drosophila, PcG proteins are bound to DNA fragments called Polycomb group respons

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

88 plex changes the positions where nucleosomes are bound to DNA, exchanges out histone dimers, and disa

89 fingers 2 and 3 (ZF2 and ZF3, respectively) are bound to DNA.

90 AVP, partially activated by being bound to DNA, excises pVIc, which binds to the AVP

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

92 two-state DNA-hairpin and a DNA hairpin that is bound to DNA origami; 2), a minor doubly labeled dsDN

93 cription factors at a distance from where it is bound to DNA, thereby enabling ICP4 to function as a

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

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

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

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

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

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

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

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

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

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

104 When a soluble fragment of TonB is bound to FecA, the transcriptional domain is displace

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

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

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

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

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

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

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

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

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

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

115 ekallikrein expresses an active site when it is bound to high-molecular-weight kininogen (HK) and can

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

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

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

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

120 interest in the inverse RNA folding problem is bound to increase.

121 ded helical conformation adopted when alphaS is bound to intact vesicles or membrane tubules.

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

123 The iron hemes of MtrA are bound to its polypeptide chain via proximal (CXXCH)

124 on in cis Cdc20 autoubiquitination while it is bound to its activator-binding site on the APC core.

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

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

127 ng X-ray crystallography that several DBMIBs are bound to KaiA dimer.

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

129 rotein convertase subtilisin/kexin 9 (PCSK9) is bound to LDL, thus we predicted that LA would also re

130 uenching property of tryptophans in NPs that were bound to ligands in a 96-well-plate-based drug scre

131 Excess histones H2A, H2B, and H2Av are bound to lipid droplets, ubiquitous fat storage orga

132 tion and ion channel activities both when it is bound to lipids at low affinity sites and when it is

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

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

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

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

137 de or inside and natural or outside the mind is bound to misfire.

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

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

140 cleotides suggest that both ATP and ADP must be bound to MutS during its conversion to a sliding clam

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

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

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

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

145 In addition, Mod5 is bound to nuclear pre-tRNA transcripts, although they

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

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

148 ween the two lobes of the ISW2 ATPase domain is bound to nucleosomal DNA and Isw2 associates with the

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

150 orted a model wherein one monomer of TRN-SR2 is bound to one monomer of RanGTP.

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

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

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

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

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

156 In HEK293 cells, the vast majority of TUG was bound to p97.

157 Analytes are bound to paramagnetic particles via antibodies and d

158 amounts of cellular Mn(II) in D. radiodurans are bound to peptides and proteins.

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

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

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

162 tely 99% of the circulating thyroid hormones are bound to plasma proteins, including three major thyr

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

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

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

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

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

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

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

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

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

172 to binding GTP, a single manganese ion (Mn1) is bound to RtcB.

173 to lipids at low affinity sites and when it is bound to SecYEG with high affinity.

174 ic NR harbors three cofactors, each of which is bound to separate domains, thus forming an electron t

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

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

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

178 e-coordinate, and in H3E-RcnR the Zn(II) ion is bound to six protein ligands.

179 pK(a) of Glu-19 is decreased when troponin C is bound to skeletal troponin I and the pK(a) of His-130

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

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

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

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

184 FODE is bound to tear lipocalin in tears.

185 a prior experience allows new information to be bound to that context, leading to source memory confu

186 When mRNA and deacylated tRNAs are bound to the 70S ribosome and EF-G-GTP is added, bas

187 Peptides are bound to the active site of the enzyme by forming an

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

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

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

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

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

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

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

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

196 Both Hsp90 and Hsp70 are bound to the expressed nNOS oxygenase domain, which

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

198 hod to distinguish phosphorus fractions that are bound to the inorganic soil components from those fr

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

200 yanides (CN(-)) and one carbon monoxide (CO) are bound to the iron and apparently account for the com

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

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

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

204 rs are Cu(II) or Zn(2+), the triazole groups are bound to the metals.

205 urier maps show that the cognate nucleotides are bound to the open state of the polymerase.

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

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

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

209 significantly more restricted when the dyes are bound to the surface of the cross-beta-subunits or t

210 dicate that, within error, 18-20 Mg(2+) ions are bound to the T40 strand at saturation and that the m

211 munoprecipitation evidence that PcG proteins are bound to the Thor 5' region in vivo.

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

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

214 C/EBPalpha and GR were found to be bound to the 11beta-HSD1 promoter.

215 However, substrate must be bound to the ASB domain for serine to exert its effec

216 lectrode and protein is that the protein can be bound to the electrode in a favourable orientation.

217 ment whereby the poisoning agent is shown to be bound to the Fe NPs.

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

219 However, to perform its function, SlmA must be bound to the nucleoid.

220 mine the number of probe molecules which can be bound to the polymer surface.

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

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

223 Conversely, SMRT is bound to the c-Fos promoter under basal conditions an

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

225 rane gate (IS6), forming an alpha-helix, and is bound to the CaVbeta subunit.

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

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

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

229 indicate that the substrate nucleotide unit is bound to the enzyme surface.

230 WAC is bound to the Golgi by GM130.

231 with high catalytic efficiency even when GDP is bound to the GTPase and hence can inhibit binding of

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

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

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

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

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

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

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

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

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

241 prevent binding of L1 to Pd, once the ligand is bound to the metal, these heterocycles do not displac

242 two major isomers, PtAN3 and PtAN1, where Pt is bound to the N3 and N1 positions of native adenine, r

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

244 22 and 1660 cm(-1), and a second NO molecule is bound to the nonheme Fe(B) site with a nu(NO)(FeB) at

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

246 When the TonB(33-239) dimer is bound to the outer membrane transporter, DEER shows t

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

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

249 he total mass of magnetic nanoparticles that is bound to the plasma membrane and internalized by cult

250 The aptamer is bound to the pore by hybridization to an oligonucleot

251 Notably, Pitx1 is bound to the previously identified HLEA and HLEB hind

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

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

254 hat YxeB binds only FO, not Cr-DFO, when DFO is bound to the protein.

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

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

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

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

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

260 ccharide, the beta1-6-branched GlcNAc moiety is bound to the sugar acceptor binding site of the beta4

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

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

263 ator-pol II-TFIIF assembly in which Mediator was bound to the activation domain of viral protein 16 (

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

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

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

267 facilitated transport even when beta-catenin was bound to the Arm-binding partner LEF-1, and its acti

268 les containing V. cholerae O139, the antigen was bound to the colloidal gold-conjugated MAb to form a

269 ipitation assay, we also showed that CHOP-10 was bound to the eNOS promoter.

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

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

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

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

274 When pre-SufI was bound to the translocon, FRET was observed for both

275 cription factors showed Pu.1, Fli-1, and Erg were bound to the -10E element, and mutation of three hi

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

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

278 K (circadian locomotor output cycles kaput), were bound to the core enhancer (CE) of the MyoD gene in

279 nd considerable amounts of phenolic residues were bound to the HAs, independent of the solution pH.

280 MLL2 and MLL3 were bound to the HOXC6 EREs in an E2-dependent manner.

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

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

283 ith neutrophil extracts, HNP-1 through HNP-3 were bound to the periphery of the growing cell colonies

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

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

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

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

288 We propose that adaptors may need to be bound to their cargo to regulate EH domain proteins a

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

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

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

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

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

294 Ssb is bound to translating ribosomes via ribosome-associate

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

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

297 gly, only one-fourth of alpha-actinin dimers were bound to two actin filaments.

298 is sterically blocked when the cognate tRNA is bound to TyrRS, we hypothesized that the nuclear dist

299 he 1:2 species, that the bidentate arsenates were bound to uranium with one of the binding oxygen ato

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

301 tions, both enzymes are fully functional and are bound to VhuD in substoichiometric quantities.