ライフサイエンスコーパス: interaction

1 MAVS in microsomes, blocking the RIG-I/MAVS interaction.

2 ation is likely due to the electron-electron interaction.

3 Mutations in these regions abolish their interaction.

4 compact global architecture primed for SUMO interaction.

5 o the crucial role of the photocatalyst-base interaction.

6 oping that sheds light on the nature of this interaction.

7 sing both vessels and tubules with potential interaction.

8 sis, video summarization, and human-computer interaction.

9 s in the presence of general quartic contact interactions.

10 might underestimate the impact of secondary interactions.

11 evolutionary dynamics resulting from biotic interactions.

12 haviors such as learning, memory, and social interactions.

13 s, and increased nestedness with mutualistic interactions.

14 strategy to better understand host-pathogen interactions.

15 nge the theoretical description of molecular interactions.

16 among the largest measured for amide-NH...F interactions.

17 tain from her cooperative behavior in future interactions.

18 hods to systematically identify such extreme interactions.

19 of a neighboring one via Coulombic electron interactions.

20 that identifies biomarkers' main effects and interactions.

21 licated by the long-ranged nature of dipolar interactions.

22 y in subjects with lower spontaneous network interactions.

23 p mediated by hydrogen bonds and hydrophobic interactions.

24 ss spectrometry was used to map their mutual interactions.

25 , including salt bridges, H-bonds, and polar interactions.

26 al progress in understanding host-microbiota interactions.

27 cterization of biologically relevant GBP-GSL interactions.

28 ind plays a fundamental role in human social interactions.

29 individuals invest time and energy in social interactions.

30 for cis-eQTLs and RNA-binding protein (RBP) interactions.

31 tors that regulate stimulation-dependent E-P interactions.

32 268 pathogens, tested on 210 hosts in 13,801 interactions.

33 change the incentive structure of strategic interactions.

34 [log10(P/B ratio) and/or AMY1 CN] diet-group interactions.

35 L and trained them to lever press for social interaction (6 d) and then for methamphetamine infusions

36 ely predicting the affinities of PBD-peptide interactions across multiple protein families.

37 levant cell types, cell states, and cellular interactions across transitions.

38 s both the wild-type and oncogenic KRAS-AGO2 interaction, albeit under different conditions.

39 of the multivariate physical challenges and interactions among challenges in high-elevation streams,

40 itrogen deposition, yet few studies evaluate interactions among these changing conditions.

41 Interaction analyses suggested an association with road

42 l surfaces to directly measure Syt1-membrane interaction and fully map the site-binding energetics of

43 formation, at the timescale of online social interaction and joint action.

44 rich domain to be dispensable for both HSP90 interaction and PDE6 activity.

45 stress confirmed that KEAP1 sheds many basal interactions and becomes associated with known lysosomal

46 ow how numerous NEDD8-dependent interprotein interactions and conformational changes synergistically

47 ish a mechanistic understanding of LBL-lipid interactions and create a modified BoNT/B with improved

48 and can dictate both the rates of ecological interactions and long-run dynamics of interacting popula

49 membrane proteins, is preserving noncovalent interactions and maintaining native-like structures.

50 n human tissues, showed long-range chromatin interactions and mRNA abundance associations with target

51 TRPC1 and PKCdelta interactions and phosphorylation of TRPC1 induced by sto

52 ation profiles to all RNAs, confirming known interactions and predicting new associations.

53 ition, bearing consequences in pollen-stigma interactions and PT guidance.

54 nty may affect the dynamics of interspecific interactions and shape the course of evolution within sy

55 y on plant fitness trade-offs, intraspecific-interactions, and soil nutrient dynamics in the context

56 , centuries and beyond), continued shifts in interactions appear to reshape network structure, leadin

57 , it can deliver comprehensive results where interactions are classified into four types, according t

58 It is found that biquadratic exchange interactions are essential to quantitatively describe th

59 Furthermore, systematic studies of these interactions are revealing that proteins may exhibit dif

60 o the chemical features required for optimal interaction at the binding site.

61 tate real-time communication between protein interactions at distinct sites.

62 on to sites corresponding to heme-CPR domain interactions at the dimeric interface.

63 between A33 and A34 and another simultaneous interaction between all three of the glycoproteins.

64 We report a plant-beneficial interaction between Arabidopsis thaliana and the root mi

65 s and regulatory network analysis infers the interaction between astrocyte-released amyloid precursor

66 Specifically, an interaction between B2 RNA and the Polycomb protein, EZH

67 l integration to characterize the functional interaction between basal ganglia and thalamus, we demon

68 s that at high enough cell concentration the interaction between boundary-following cells leads to fo

69 essential role of YTHDF3 in controlling the interaction between cancer cells and brain microenvironm

70 These findings reveal how an interaction between cells in different EMT states confer

71 Together, our findings highlight the novel interaction between endocan and EGFR and new opportuniti

72 wo spatial coding modes was supported by the interaction between excitatory gamma inputs and local in

73 Complex interaction between genetics, epigenetics, environment,

74 Data suggest that interaction between gingivitis and obesity may exhibit d

75 The interaction between ischemic time and alteplase dose was

76 tage of the well-described and high-affinity interaction between KRAS and CRAF, and we provide high-r

77 of "anode-free" Li batteries to minimize the interaction between LMA and electrolyte, approaches to e

78 Lastly, we show a direct interaction between Med19 and Med1 by GST pulldown exper

79 There was no evidence of interaction between MRD status and conditioning regimen

80 We identify a pH-sensitive electrostatic interaction between positively charged arginine in extra

81 nts with current history presented increased interaction between putamen and globus pallidus internus

82 There was no apparent interaction between Px and Iso treatment.

83 tion, a strong antagonistic (i.e. dampening) interaction between sportfish predation and warmer tempe

84 The interaction between tau and LRP1 is mediated by lysine r

85 Finally, the interaction between telomere attrition from 4 to 18 mont

86 m depends on the change in the electrostatic interaction between the charges on each end of the bridg

87 and globus pallidus internus, and decreased interaction between the latter and the thalamus, compare

88 Biophysical insight into the binding interaction between the major whey protein, beta-Lactogl

89 ection and provide insights into the complex interaction between the virus and innate receptors that

90 Here we analyzed the interaction between transformed and wild-type NSCs isola

91 Here we investigated the interaction between vancomycin and VanS from Streptomyce

92 out mice-indicating a functional and genetic interaction between Xinbeta and YAP.

93 d by docking results demonstrating favorable interactions between 4-allyl-2,6-dimetoxypheno and the N

94 where reactions rely on reversible covalent interactions between an organic substrate and a chiral m

95 However, the evolutionary interactions between antibiotics and phages remain uncle

96 ngle molecule level details on the potential interactions between different peptides and the main ant

97 Interactions between disordered proteins involve a wide

98 tro and in cells to elucidate details of the interactions between Fe(2+) and the ribosome and identif

99 To address how interactions between four key TFs contribute to cis-regu

100 complex inflammatory disorder with multiple interactions between genetic, immune and external factor

101 ht loss and metabolic responses depends upon interactions between genetic, phenotypic, and environmen

102 Crucially, protein-protein interactions between hGrx1, Atox1 and WLN5-6 were detect

103 Further, we tested direct interactions between inner and outer photoreceptors usin

104 However, establishing long-range interactions between multiple dopants or defects is chal

105 m patients with CALR-mutated MPNs, defective interactions between mutant calreticulin, ERp57, and STI

106 ocal or bloodstream, the consequences of the interactions between platelets and a tumor may promote o

107 capable of detecting and quantifying lateral interactions between proteins on membranes.

108 The promotion of mixed-valence interactions between redox-active, pai-conjugated scaffo

109 this theoretical model to test the possible interactions between tau proteins and amyloid-beta and s

110 and visual discrimination memories depend on interactions between the hippocampus (HPC) and other mem

111 he entorhinal cortex is the main gateway for interactions between the neocortex and the hippocampus.

112 The CDs facilitate the electronic interactions between the phthalocyanines.

113 reactions for each step, the intermolecular interactions between the substrates, and the triplet sta

114 We identified potential angiocrine interactions between tissue-specific ECs and other cell

115 porating a term for treatment assignment and interactions between treatment and baseline covariates.

116 Store depletion induced interactions between TRPC1 and PKCdelta and PKCdelta-dep

117 ost-guest interaction (e.g., Lewis acid-base interaction), between F(-) and MOF host, a highly select

118 d the disruption of a C(32-)A(38) cross-loop interaction but failed to fully explain the means by whi

119 1/92 [66%] vs 84% [391/465] P < 0.001, P for interaction by regimen 0.49).

120 es occurring during host-microbiota-pathogen interactions can favorably or negatively influence host

121 h production, while changes in predator-prey interactions cannot.

122 on of the NAD(+)-binding site or the ARM-TIR interaction caused constitutive activation of SARM1 and

123 gy is the extent to which long-range looping interactions change across developmental models, genetic

124 ntity, stoichiometry, and stability of these interactions characterized here comprehensively reveal t

125 ansient, nanoscopic lipid- and protein-based interactions confer a steady-state organization of the p

126 mproves our understanding of protein-protein interactions, contributes to the prediction of protein f

127 -body errors are small in both SCAN and self-interaction-corrected SCAN.

128 Inhibition of TWEAK/Fn14 interaction could be efficacious in anaphylaxis therapy.

129 Together, multivalent interactions couple productive binding to efficient deac

130 g molecular targets in the malaria parasite, interaction data for ligands with antimalarial activity,

131 e integration of gene expression and protein interaction data improves the robustness of prediction a

132 oint for further design of a protein-protein interaction detection system as well as novel FAP-based

133 recision and power of differential chromatin interaction detection through data augmentation under pr

134 Plant identities critical for retaining interaction diversity are similar and independent of geo

135 Here we show that heterotypic multicomponent interactions dominate endogenous LLPS, and give rise to

136 on, fluctuations, and heterochromatin-lamina interactions during nuclear remodeling.

137 tructure significantly modulates protein-RNA interaction dynamics and can facilitate real-time commun

138 Benefiting from the unique host-guest interaction (e.g., Lewis acid-base interaction), between

139 Interaction effects can change materials properties in i

140 the relative accessible surface area and the interaction energy, can help characterize a protease's s

141 replicable interactions shared by chromatin interaction experiments.

142 ltiomics approaches to study microbiome-host interactions following chemical perturbations.

143 Mapping of digenic interactions for a deletion mutant of each paralog, and

144 ne eGFR, but suggested treatment-by-subgroup interactions for subgroups based on NYHA functional clas

145 tion mutant of each paralog, and of trigenic interactions for the double mutant, provides insight int

146 Multi-enhancer interactions formed at genomic regions harboring genes w

147 ompare the high-resolution maps of chromatin interactions from 10 tissue or cell types with a focus o

148 leotide polymorphisms can affect RNA-protein interactions from outside binding motifs through altered

149 Systematic mapping of genetic interactions (GIs) and interrogation of the functions of

150 d efforts to better understand the molecular interactions governing disease progression.

151 PO ligands, which could reveal the molecular interactions governing ligand residence time.

152 The protofibril-fibril interaction governs their temporal evolution and potenti

153 This interaction has been proposed as a potential risk factor

154 Despite this advance, few genetic interactions have been reproduced across multiple studie

155 tions to disrupt the H-bonds and hydrophobic interactions holding together the beta-sheets.

156 We test two central tenets of the biotic interactions hypothesis: that predation is (1) strongest

157 We quantified this interaction in native grassland by experimentally elimin

158 re not a definitive descriptor of O2 carrier interaction in tumor capillary networks, we accounted fo

159 been proposed that this facilitates telomere interactions in ALT+ cells.

160 a demonstrate the significance of 1,5-O...Ch interactions in enantioselective catalysis.

161 g Hi-C, reveals condensin-mediated chromatin interactions in interphase that are qualitatively simila

162 ncovered the crucial function of neuroimmune interactions in maintaining tissue homeostasis and prote

163 pounds is of importance to reveal functional interactions in microbiomes.

164 rspectives to better understand virus-glycan interactions in physiologically relevant conditions.

165 e its binding to FZD and to quantify Wnt-FZD interactions in real time in live cells, utilizing a rec

166 detects these intercellular protein-protein interactions in the less than or equal to 10 nm range.

167 Plant-microbial interactions in the rhizosphere are an essential link in

168 vention, we quantitatively imaged PD-1/PD-L1 interactions in tumor samples from patients, employing a

169 of synthetic membranes to study lipid-lipid interactions in vitro, alongside optical microscopy tech

170 forming peptides exhibit strong interpeptide interactions, including salt bridges, H-bonds, and polar

171 one of the strongest drivers of interkingdom interactions-including those between microorganisms and

172 e condensate into higher momentum states via interaction-induced fluctuations-the phenomenon of quant

173 stic insights into how SARAH domain-mediated interactions influence Hippo pathway activity.

174 from HIV.IMPORTANCE CD40-CD40 ligand (CD40L) interaction is crucial for inducing effective cytotoxic

175 However, XPRT oligomeric interaction is distinct from HPRT in that XPRT forms a s

176 systems, including the human body, but this interaction is especially complex in the primary gateway

177 However, it seems that an in-person interaction is still preferred when possible for surgica

178 The prevalence of introduced interactions is directly related to human environmental

179 matical theory to show that the rate of such interactions is inherently limited by the ability of org

180 y exposed, and the likelihood of deleterious interactions is quite high.

181 f a gene regulatory layer, a protein-protein interaction layer, and a metabolic layer.

182 gion (UTR) play an important role in Gag:RNA interactions leading to genome packaging.

183 terature which utilizes multiple noncovalent interactions like H-bonding, solvent bonding, S-H...pai,

184 a mass spectrometry (ICPMS), and hydrophilic interaction liquid chromatography (HILIC) - electrospray

185 These interactions make combined epigenetic therapy and immuno

186 e latter determined using a pairwise genetic interaction map that identifies numerous interactions th

187 Genome-wide chromatin interaction mapping, using Hi-C, reveals condensin-media

188 ally interacts with SOS1 and SOS2, and these interactions modulate PUT3 transport activity.

189 th other vIRFs and other proteins, that this interaction modulates antiviral signaling via disruption

190 To capture the long-range interactions, most studies integrate bidirectional recur

191 us sources of data to construct a multilayer interaction network composed of a gene regulatory layer,

192 ty to known disease genes in protein-protein interaction networks and identified gene clusters with f

193 mpting further investigation into virus-host interaction occurring during the early stages of HIV inf

194 ranslocon is dynamic and is triggered by the interaction of a Tat substrate with the Tat receptor com

195 Characterizing the interaction of avian BST-2 with avian viruses is importa

196 Collectively, these data show a unique interaction of between pathogenic C difficile and F nucl

197 uperresolution microscopy revealed a reduced interaction of CG with the microtubule network upon a3-s

198 We explore the interaction of differential stage susceptibility and sta

199 for exploring fundamental mechanisms behind interaction of electromagnetic waves with 2D materials.

200 ow that CTM provides an important domain for interaction of HOXA1 proteins with PBX.

201 As a guest, the host-guest interaction of MPT was studied with two macrocyclic cucu

202 ork by Cory's group pointed to a synergistic interaction of MYC and MNT in neoplastic B-cell developm

203 To date, possible interaction of PIP(2) with ENaC primarily has been teste

204 Interaction of SUB2-null merozoites with RBCs leads to e

205 n the short sequence was undertaken, and the interaction of the resulting library with the protein wa

206 EK293T cells, implying that a lower-affinity interaction of the SNAP25 zDABM with zDHHC17 is optimal

207 d an inhibitory role attributed to the lower interaction of the thiocarbonyl group with the solvent i

208 ess this situation, we previously quantified interactions of alkyl ureas with amide and aromatic comp

209 range of rotaxanes, the strategy enables 1:1 interactions of crown ethers with various functional gro

210 s of combinatorial genetic and physiological interactions of different Galpha proteins with the sole

211 mportant roles in bacterial viability and in interactions of pathogenic mycobacteria with their hosts

212 l-down experiments also confirm the physical interactions of ScDmc1 with ScRad51 in solution, but not

213 Analysis of the structure and interactions of the IC from Chaetomium thermophilum demo

214 ulations were employed to study the membrane interactions of the intrinsically disordered SH4 and Uni

215 t with ubiquitin-specific protease 7 (USP7); interactions of vIRF-1 and vIRF-3 with USP7 promote PEL

216 ating the regulatory effects of the SUMO-SIM interaction on ICP0 E3 ubiquitin ligase activity regardi

217 The rs6008845-by-fenofibrate interaction on MACE was replicated in African Americans

218 the existence of two previously unidentified interactions: one between A33 and A34 and another simult

219 often show changes in populations and their interactions over time.

220 ricans, respectively (age trend P < 0.05 and interaction P = 0.041).

221 A-approved human inhaler devices followed by interaction parameter analyses.

222 sidue N-terminal region of its extracellular interaction partner CsgF to produce a dual-constriction

223 er analysis identified CofA (Cgp_0016) as an interaction partner of the peptidoglycan synthase PBP1a

224 -cell clones activated via a pharmacological interactions pathway in patients with liver injury is in

225 nted out spectacular differences in terms of interaction patterns and inhibition values between hsTYR

226 Cell-ECM (extracellular matrix) interactions play essential roles in the morphogenesis o

227 We also find that the spatio-temporal interactions posited to occur during neurogenesis are ne

228 target interactions, such as protein-protein interaction (PPI), remains to be elucidated.

229 comprehensive examination of protein-protein interactions (PPIs) is fundamental for the understanding

230 d from a genome-wide analysis of BBxgenotype interaction predicting time to all-cause mortality, adju

231 ression, demonstrating an exercise and clock interaction, providing insight into potential mechanisms

232 studies suggest that the loss of dAKAP1-RNA interactions reduces mitochondrial electron transport ch

233 ctive zones is controlled via trans-synaptic interactions remains unknown.

234 thod called IDR2D that identifies replicable interactions shared by chromatin interaction experiments

235 affinity bonds by using several weak binding interactions simultaneously.

236 We identified important protein interaction sites, in addition to sites corresponding to

237 redundant capacity for edges and capture the interaction strength of nodes.

238 an be used for pharmacokinetic and drug-drug interaction studies.

239 ortantly, the complexity of molecular target interactions, such as protein-protein interaction (PPI),

240 of sequence variability in the Spike protein interaction surface, which greatly influences Spike prot

241 However, the interaction term between annual average NDVI and APOE ep

242 t KSIs provided insights into the forces and interactions that allow and limit active-site motions.

243 n peripheral positioning to include boundary interactions that either weakly attract all chromatin or

244 ipids engage in specific, trimer-stabilizing interactions that go beyond simply providing a concentra

245 considerably broadens the class of possible interactions that result in peripheral positioning to in

246 ides a powerful tool for studying viral-host interactions that should facilitate the discovery of ant

247 gating, and reveals multiple ligand-channel interactions that stabilize this permissive conformation

248 tic interaction map that identifies numerous interactions that suppress synthetic lethal effects.

249 edge, this is the first identification of SE interactions that underlie hormonal regulation of genes

250 We focus on four key rules of life and their interactions: the temperature dependence of biotic proce

251 attempt to understand the neural-cell-immune interaction to investigate the underlying mechanism of n

252 y change involved changes in protein-protein interactions to favor Cas2 binding over tetramerization;

253 heir confinement and favorable electrostatic interactions to finely control nucleotide signaling.

254 may be common in multivalent WW domain-PPXY interactions to promote the adaptability and versatility

255 r contributed by biasing the remodeler-actin interaction toward nucleosomes with the non-canonical hi

256 Se and Te ore levels before and after fungal interaction using X-ray fluorescence, laser ablation ind

257 The PD-1/PD-L1 interaction was not correlated with clinical PD-L1 expre

258 del reflecting perceived frequency of social interaction was present beginning at ~110 ms, even in th

259 d for multiple other of the 56 cross feeding interactions we study.

260 These interactions were not detected in cognitively normal old

261 Strikingly, almost half of the interactions were not previously detected by two-hybrid

262 Cannabis use by risk group interactions were observed in the striatum and OFC.

263 tension sensation or enrich for p38-YAP-TEAD interactions, which explains the topography-dependent di

264 Advancing understanding of neuron-cancer interactions will elucidate new therapeutic strategies f

265 ntiality of c-di-AMP does not result from an interaction with a single essential target but rather fr

266 f the actin-binding regions promoting myosin interaction with actin, which could explain the observed

267 We assessed PRS(313) interaction with age at first diagnosis, family history,

268 AM1 variants cause JBTS and disrupt TOGARAM1 interaction with ARMC9.

269 mage caused by atorvastatin depending on its interaction with CDC: Preparations responding to CDC wit

270 more, the TPH2 genotype showed a significant interaction with childhood trauma in predicting worse sy

271 al ICAM-1 and VCAM-1 was confirmed by T-cell interaction with EECM-BMEC-like cells.

272 ltimerization also makes Aire susceptible to interaction with promyelocytic leukemia protein (PML) bo

273 The study of beta-carotene interaction with proteins showed, on the one hand, a neg

274 e S1 SARS-CoV-2 spike protein, and block the interaction with the human ACE2 receptor.

275 ease and is assumed to cause toxicity by its interaction with the neuron membrane.

276 d to microvilli in the absence of any direct interaction with the other IMAC components.

277 polyphenols adsorption increase due to their interactions with albumin.

278 Interactions with auxiliary subunits and other factors m

279 their chemical speciation in solution, their interactions with bentonite, and their sorption potentia

280 xible" linear polymer backbone to facilitate interactions with biomembrane systems, and (ii) "rigid"

281 How these regions and their interactions with brain-wide activity drive action selec

282 e, influencing adaptive immune responses via interactions with dendritic cells (DCs).

283 orrelate with the local environment or their interactions with different neuron types.

284 f the atomic force microscope to investigate interactions with glycans at the single-virion level dir

285 s antiviral signaling via disruption of USP7 interactions with innate immune signaling proteins TRAF3

286 olidation processes by targeting hippocampal interactions with lateral occipital cortex (LOC).

287 s, to provide meaningful insights into their interactions with ligand molecules.

288 to geographic genetic variation and climate interactions with other aspects of environment.

289 USP7, via a means distinguishable from USP7 interactions with other vIRFs and other proteins, that t

290 d the hairpin, exhibited hormone-independent interactions with PhMAX2A and PhD53A, respectively.

291 potassium channel (Kir) Kir2.2 has multiple interactions with plasma membrane lipids: Phosphatidylin

292 of lipid-lipid, lipid-protein, and lipid-dye interactions with single-molecule, nanoscale resolution.

293 el insight into a possible mechanism for CBD interactions with sodium channels.

294 nct cell types with differing capacities for interactions with stromal cell types.

295 and brainstem nuclei, which mediate complex interactions with the brain's cortical processing hierar

296 ibits altered fluorescence in response to LD interactions with the lysosome.

297 LSVs to acute arterial WSS promoted monocyte interactions with the vessel lumen.

298 l that combines polarity protein biochemical interactions with vesicle trafficking to probe how vario

299 th amide and aromatic compounds, relative to interactions with water.

300 Our method, PIZSA (Protein Interaction Z-Score Assessment), is a binary classificat