ライフサイエンスコーパス: molecular interaction

1 ydrophilic moieties with potential points of molecular interaction.

2 to full-length LRP1 to gain insight into the molecular interaction.

3 gulates beta2 integrin function via a direct molecular interaction.

4 by the pY mimic that underpin this improved molecular interaction.

5 s controlled by auto-inhibition via an intra-molecular interaction.

6 t, offering new insight into the close-range molecular interaction.

7 n the mature part, possibly through a direct molecular interaction.

8 can provide key insights regarding specific molecular interactions.

9 ot always explain the full complexity of the molecular interactions.

10 is compact, with a self-contained system of molecular interactions.

11 bling DNA-based nanosystem for interrogating molecular interactions.

12 and shows specificity in its large range of molecular interactions.

13 roteins in HCV replication and delineate the molecular interactions.

14 to an average measurement of the ensemble of molecular interactions.

15 data types to derive computational models of molecular interactions.

16 anoRx formulations for desired and undesired molecular interactions.

17 bing self-association, aggregation and inter-molecular interactions.

18 lectrostatic repulsive forces and attractive molecular interactions.

19 rain at breaking by taking advantage of weak molecular interactions.

20 amine to be recognized via identical sets of molecular interactions.

21 nteractome, the map of biologically relevant molecular interactions.

22 r of oocyte polarity, acting through unknown molecular interactions.

23 al biology is knowledge of the energetics of molecular interactions.

24 o perturbations starting from the underlying molecular interactions.

25 or registration compatible with the scale of molecular interactions.

26 obalance (QCM), both applied to quantify the molecular interactions.

27 omposition, hydration states, structure, and molecular interactions.

28 ires an intimate understanding of the glue's molecular interactions.

29 de pairs containing 245 intra- and 398 inter-molecular interactions.

30 the nanomaterial's surface chemistry via the molecular interactions affecting the hydrogen-bonding ne

31 important for understanding the physical and molecular interactions among its members.

32 Recent studies have shown the importance of molecular interactions among microbiota, enteric neurons

33 While the molecular interactions among p53 and microRNAs have emer

34 ssembly is tightly controlled by multivalent molecular interactions among RNA molecules, adaptor prot

35 Using a molecular interaction analysis system, we confirmed that

36 The diversity of expression, molecular interaction and phenotype of rtcs and rtcl wer

37 molecular species, as well as to probe inter-molecular interactions and can be used to estimate the a

38 blies from which one can learn principles of molecular interactions and chemical activities.

39 ncurrent but differentiated intra- and inter-molecular interactions and develop an encounter complex-

40 Rs, and stochastic fluctuations arising from molecular interactions and diffusion do not average out.

41 nce correlation spectroscopy, to measure the molecular interactions and full coexistence curves (bino

42 allergy have revealed the atoms involved in molecular interactions and mechanisms of disease.

43 he manner by which salt addition affects the molecular interactions and morphology of condensed starc

44 interaction network analyses, we identified molecular interactions and pathways elucidating the meta

45 X facilitates investigations of host-microbe molecular interactions and provides insights into a rang

46 ics simulations to investigate in detail the molecular interactions and residues involved in such a c

47 res give unprecedented atomic details of the molecular interactions and show how the inhibitors effic

48 e emerged as a powerful tool for controlling molecular interactions and signalling cascades at precis

49 Using the Michigan Molecular Interactions and STRING databases and the MoCh

50 , predict and experimentally confirm a novel molecular interaction, and determine which pQTLs are ass

51 Viscosity, molecular interactions, and flocculation were the most i

52 tion for posing more complex questions about molecular interactions, and have led to the discovery of

53 ur findings shed light onto SWCNT/dispersant molecular interactions, and introduce a versatile approa

54 In rule-based modeling, molecular interactions are systematically specified in t

55 resemble JAK2 JH2, but distinct stabilizing molecular interactions around helix alphaAL in the activ

56 mplexes can be imaged in isolation to reveal molecular interactions at different states.

57 -time characterization and quantification of molecular interactions at interfaces, the detection of s

58 olonization and infection depend on specific molecular interactions at the host-microbe interface tha

59 understanding to advance the engineering of molecular interactions at the nanoscale.

60 , have seen little work done to characterize molecular interactions at their surfaces.

61 technique can be applied to a wide range of molecular interactions because the nanophotonic tweezer

62 Here, we characterize the molecular interaction between (p)ppGpp and guanylate kin

63 is described to precisely perturb a specific molecular interaction between adeno-associated virus and

64 iated by ArfA and RF2 has been reported, the molecular interaction between ArfA and RF2 in the riboso

65 To clarify the early molecular interaction between ectomycorrhizal partners,

66 Here, we deciphered the molecular interaction between fibronectin and pneumococc

67 Co-immunoprecipitation demonstrated a molecular interaction between LTBP4 and TGFBR2.

68 Finally, we evaluated in vitro the molecular interaction between LXA4 and glucocorticoid re

69 Moreover, molecular interaction between subunitsB2andC1and actin w

70 ate endosomal maturation that involves a new molecular interaction between the tethering factor Munc1

71 within the embryo, highlighting the complex molecular interaction between these two tissues during e

72 We show that there is a direct molecular interaction between TSP4 and Cavalpha2delta1 i

73 The molecular interaction between viral RNA and the cytosoli

74 biophysical studies to better understand the molecular interactions between a potent bis-pyridylurea

75 Insight into the molecular interactions between AKR1B1 and PGA1 was advan

76 Here we describe the molecular interactions between AmpR (from Citrobacter fr

77 In order to better understand the molecular interactions between antivenom antibodies and

78 Controlling molecular interactions between bioinspired molecules can

79 easing interest focusing on the cellular and molecular interactions between cancer cells and their mi

80 identify and annotate previously undescribed molecular interactions between capsid subunits that are

81 To assess for potential molecular interactions between D1R and D2R we also emplo

82 hese results provide insight into the unique molecular interactions between DNA and the SWCNT surface

83 nt in SERS spectra provides insight into the molecular interactions between functionalized nanopartic

84 Favorable molecular interactions between group 16 elements have be

85 Molecular interactions between heterologous classes of f

86 resent structural and functional analyses of molecular interactions between human VPS4, LIP5, and the

87 health and disease, and to decipher complex molecular interactions between humans and other species,

88 While the molecular interactions between individual myosin motors

89 ed, it is necessary to better understand the molecular interactions between influenza viruses and the

90 Here, we studied the molecular interactions between IST1 and the three MIT do

91 ive site geometry and the rupture of crucial molecular interactions between key residues in both the

92 The molecular interactions between macrophage colony-stimula

93 In the present study, we characterized molecular interactions between MFAP4 and elastic fiber c

94 tures reveal for the first time the detailed molecular interactions between MG antibodies and a core

95 To elucidate direct molecular interactions between multiple regulatory facto

96 The detailed molecular interactions between native HIV-1 capsid prote

97 Using a proteomic approach we now report molecular interactions between nuage proteins and compon

98 d thereby increase tumor growth, the precise molecular interactions between platelets and metastatic

99 will highlight current understanding of the molecular interactions between PMNs and mucosal epitheli

100 sion, our study suggests a common pattern of molecular interactions between pneumococcal FnBPs and fi

101 Some molecular interactions between polymer chains and antiox

102 Molecular interactions between proteins and DNA molecule

103 In the present study, we characterized molecular interactions between receptors and co-receptor

104 The molecular interactions between reproductive cells are cr

105 Here we identify molecular interactions between specific residues in the

106 in proximities, leading to identification of molecular interactions between subunits, insights into t

107 uide to PHARMACOLOGY provides expert-curated molecular interactions between successful and potential

108 Molecular interactions between TGF-beta pathway and VDD

109 The molecular interactions between the ligands and TTR were

110 C1A cysteine protease fold with a network of molecular interactions between the N-terminal propeptide

111 It is increasingly clear that molecular interactions between the nervous system and mi

112 uterium exchange mass spectrometry to define molecular interactions between the specific human isofor

113 exual reproduction and comprises a series of molecular interactions between the sperm and egg.

114 mal functions of progranulin and TDP-43, the molecular interactions between these proteins remain unc

115 However, an analysis of the molecular interactions between these subunits in mammals

116 Mucosal homeostasis depends on physical and molecular interactions between three components: the res

117 Here we successfully probed the molecular interactions between two peptides (cecropin P1

118 to be affected by variability in the initial molecular interactions between virus and host.

119 Although broad, these molecular interactions, both at the chromatin and RNA le

120 lar and organic systems via intra- and inter-molecular interactions, but study of inorganic materials

121 ccur in a sequential manner to ensure proper molecular interactions, but the underlying mechanism rem

122 logous and heterologous fibril growth; thus, molecular interaction can constitute a link between diff

123 most important conformational information in molecular interactions can be captured by THz electromag

124 ess of the polypeptide and strength of inter-molecular interactions- can give rise to many of the str

125 These findings suggest that specific molecular interactions control TRPV1 activation by parti

126 ilt and analysed a mathematical model of the molecular interactions controlling the G1/S and G2/M tra

127 ddition, integration of gene expression with molecular interaction data highlights nodes that, althou

128 ection of human (as well as mouse and yeast) molecular interaction data integrated from 32 different

129 The IntAct molecular interaction database has created a new, free,

130 toskeleton, lipid composition, crowding, and molecular interactions deviate lateral diffusion from th

131 Molecular interactions driving FGF2 monomers into membra

132 lecular mobility and how mobility relates to molecular interaction dynamics and bioactivity in living

133 It describes the direct mechanisms (molecular interactions, enzymatic conversion, salting-ou

134 By using molecular interaction fingerprints, we discovered that t

135 essment of the global dysregulation of their molecular interactions following compound perturbation.

136 urement and the successful detection of both molecular interactions (for example, cleavage, binding,

137 nerally governed by a complex competition of molecular interaction forces acting in such three-phase

138 efficiency (E) and the affinity (Kd) of the molecular interaction from intermolecular FRET signals i

139 sight into the mechanism by which IDP-driven molecular interactions give rise to liquid phase organel

140 Long and short range molecular interactions govern molecular recognition and

141 The molecular interactions governing the early events of ost

142 (AD), yet a systematic investigation of its molecular interactions has not been reported.

143 tes lymphangiogenesis, because these complex molecular interactions have been difficult to follow ex

144 Numerous cellular and molecular interactions have been identified by which imm

145 and quantitative comparison, we investigated molecular interactions important for the regulatory role

146 lded a complete thermodynamic profile of the molecular interaction in agreement with published data.

147 ity to rapidly and specifically antagonize a molecular interaction in vitro and follow a biological p

148 i-layer network, where each layer represents molecular interactions in a different human tissue.

149 d to identify and characterize molecules and molecular interactions in a wide range of applications,

150 Mechanical force regulates a broad range of molecular interactions in biology.

151 g it a unique bioorthogonal atom for probing molecular interactions in biology.

152 ned by an understanding of the collective of molecular interactions in form of biological networks.

153 Modeling multivalent molecular interactions in granules is challenging becaus

154 id and sensitive technique for investigating molecular interactions in inflammasome formation, by com

155 However, mosquito-malaria molecular interactions in nature are not clear.

156 oscale organization, topology and synergy of molecular interactions in signalling complexes downstrea

157 challenge of cell biology is to investigate molecular interactions in subcellular compartments of li

158 en a new pathway for the study of ultra-weak molecular interactions in surface-bound protein-ligand c

159 s were performed to investigate time-evolved molecular interactions in systems containing fullerenes

160 olite formed by sofosbuvir, to elucidate key molecular interactions in the active site.

161 haracterization is important in the study of molecular interactions in the cell, including the regula

162 ns was combined with an understanding of the molecular interactions in the crystal lattice to improve

163 applicable toolbox for the investigation of molecular interactions in the cytoplasm of living cells.

164 tomic models of both states reveal conserved molecular interactions in the interior of the filament a

165 ects (VPIE) have been observed, depending on molecular interactions in the liquid phase and the inves

166 2 interactions, suggesting the importance of molecular interactions in the sensitization route.

167 Using the detailed information about the molecular interactions in two filament states, we succes

168 he presumptive altered dynamics of transient molecular interactions in vivo contributing to neurodege

169 It has been used previously to model complex molecular interactions including the motion of a myosin-

170 ome locations by a range of well-established molecular interactions, including protein binding with r

171 the receptor have been well-documented, but molecular interactions involved in receptor activation r

172 We show that FLA4 acts predominantly by molecular interactions involving its carboxy-proximal fa

173 e absence of Arg-147 suggesting that this bi-molecular interaction is not involved in further stages

174 pretation of predictive features using known molecular interactions is desired.

175 . and graphene, therefore understanding such molecular interactions is essential.

176 ins can be directly displayed on an uploaded molecular interaction map, allowing users to systemicall

177 cycle events are consistent with established molecular interaction maps.

178 helical SARAH domains, though the underlying molecular interaction mechanism is unclear.

179 sociated protein complexes shed light on the molecular interactions mediated by 'hotspots' of the SF3

180 n of these mutants, we propose a sequence of molecular interactions mediated by Synaptotagmin that pr

181 aken together, our results indicate that the molecular interactions mediating the aggregation state o

182 To gain insight into the cellular and molecular interactions mediating the desmoplastic reacti

183 mbrane curvature in orchestrating the myriad molecular interactions necessary for the success of clat

184 ual protein under study and intra- and inter-molecular interactions need to be differentiated properl

185 edicting gene (or protein) function based on molecular interaction networks has become an important t

186 ws users to obtain, visualize and prioritize molecular interaction networks using HD-relevant gene ex

187 to account for the topological structure of molecular interaction networks, we developed an optimisa

188 ds for integrating disparate omic data using molecular interaction networks, with a view to gaining m

189 d that permit detailed analyses across broad molecular interaction networks.

190 The elucidation of Gp45-involved molecular interactions not only broadens our understandi

191 provide the first structural evidence of the molecular interaction occurring between isomalto-oligosa

192 promoters, obtaining a detailed view of the molecular interactions occurring at Brf2-dependent Pol I

193 These results increase understanding of the molecular interactions occurring between transcription f

194 lucidated sequential events and cellular and molecular interactions occurring during crescentic lesio

195 Our studies demonstrate a molecular interaction of Brg1 and FoxM1 and an endotheli

196 roscopy, we reveal clear distinctions in the molecular interaction of different ligands with the chan

197 This protective effect is restricted to the molecular interaction of IL-17A and/or IL-17F with the I

198 TRX2 affected proper folding or intra-/inter-molecular interaction of Mst7 and expression of the domi

199 sis of structural analogs suggested that the molecular interaction of NeoB with LXR correlated with t

200 Our data provides evidence of a molecular interaction of PSEN1 and alpha-synuclein that

201 Direct molecular interaction of the SEC, cohesin and RNAP2 was

202 ows us to propose a structural model for the molecular interaction of the SpGAPDH-Plg complex.

203 pport for using model membranes to study the molecular interactions of AMPs with bacterial membranes.

204 The molecular interactions of both enantiomers 6c and 6d at

205 ructures, and their implication for modeling molecular interactions of chemokine receptors with small

206 a unique opportunity to unravel the specific molecular interactions of collagen fibrillogenesis.

207 Further information regarding the molecular interactions of components and overall network

208 This study probed the molecular interactions of diverse polyphenols with cellu

209 Molecular interactions of gas-phase nonylphenols (NPs) w

210 interact with Arg(315), thus elucidating the molecular interactions of KD-247 with its V3 loop target

211 Here, the molecular interactions of murine GBPs (mGBP1/2/3/5/6), h

212 We explore the key molecular interactions of NEMO using a molecular biophys

213 onformational change are at the heart of the molecular interactions of NEMO.

214 cture, function, conformational changes, and molecular interactions of outer membrane proteins can be

215 permits analysis of structure, dynamics, and molecular interactions of proteins.

216 co-crystal structures revealed differential molecular interactions of the 20S-OH moiety and the 25-O

217 l domains, determine the localization and/or molecular interactions of the filaments.

218 tion, thus revealing some flexibility in the molecular interactions of the FXI apple 2 domain.

219 ydrophobic isopropyl side groups, as well as molecular interactions of the polymer's amide moieties.

220 Moreover, we discuss the emerging molecular interactions of these angiogenic cues with the

221 d P. americana for cancer treatment, but the molecular interactions of these products are unknown.

222 ved cell adhesion complex to orchestrate the molecular interactions of three tissues during patternin

223 increased rapidly, and our knowledge of the molecular interactions of tospoviruses with their host p

224 g in a labeled amino acid that can mimic the molecular interactions of Trp, enabling wash-free imagin

225 e structure of the Gag-Pol substrate, or the molecular interactions of viral structural proteins.

226 e scale using unique probabilistic models of molecular interactions on a per-sample basis.

227 d assess dilute adsorbed molecules and their molecular interactions on low-surface-area materials, no

228 interstitial space and the limiting rate of molecular interactions or conformational changes in the

229 is, independent of the underlying details of molecular interactions or spatial stacking.

230 the response to environmental stress through molecular interactions outside of the nucleus.

231 put MITOMI (mechanically induced trapping of molecular interactions) platform, we derived equilibrium

232 o host Apolipoprotein H (ApoH) and that this molecular interaction plays a pivotal role for successfu

233 These data reveal previously unappreciated molecular interactions regulating HER2 localization, mem

234 However, critical details of the associated molecular interactions remain unclear.

235 dies provide the first atomic insight into a molecular interaction required for mitotic centrosome as

236 nucleocapsid transit in infected cells, the molecular interactions required for their function are u

237 To understand the molecular interactions required for these activities, we

238 omplex with preferred sequences revealed the molecular interactions responsible for these affinity ch

239 ng stone towards the rational engineering of molecular interaction(s) with acid sites in zeolitic cat

240 In this review, we highlight some of the key molecular interactions, some of which are already showin

241 f nanoRx with regard to engineering specific molecular interactions, SPR can rapidly quantify small a

242 The in vitro and in vivo molecular interaction studies show that SHW1 physically

243 network obtained from normal, non-cancerous molecular interactions such as signal transduction and t

244 eagents targeting the disruption of specific molecular interactions suggested that pressure-induced a

245 ns from both intrinsic flexibility and inter-molecular interactions than conventional NMA only consid

246 ues at the amino-terminus instigate an intra-molecular interaction that enlists both of the N-termina

247 phomagenesis, these findings expose a unique molecular interaction that may represent a viable target

248 The molecular interactions that allow NPC cells to evade imm

249 tal iron and sulfur to scaffold proteins via molecular interactions that are still poorly defined.

250 ity involves complex, time-dependent dynamic molecular interactions that cannot be observed directly

251 recent seasonal influenza virus HAs, but the molecular interactions that contribute to HA stability a

252 woody plant biomass, with an emphasis on the molecular interactions that contribute to its recalcitra

253 Using a cell-free gene network we programmed molecular interactions that control the frequency of osc

254 border assembly, reveals a hierarchy in the molecular interactions that drive intermicrovillar adhes

255 We provide a detailed description of the molecular interactions that drive the membrane crossing

256 ur kinetic and biochemical data, reveals the molecular interactions that enable ArfA to specifically

257 ne adopts a specific orientation to form the molecular interactions that facilitate its passage throu

258 Although much is known about the molecular interactions that govern the regulation of key

259 Assessment of molecular interactions that may contribute to these acti

260 solvent accessibility of Tyr168 in promoting molecular interactions that may lead to prion protein mi

261 several classes of physiologically important molecular interactions that occur between bacteria and t

262 pectrum aptamers to overcome resistance, and molecular interactions that occur during viral assembly.

263 -term goals of our laboratory is to identify molecular interactions that regulate metastasis, as a ba

264 and define a framework of early cellular and molecular interactions that regulate T cell alloimmunity

265 (NK) cell development have been defined, the molecular interactions that shape human NK cell maturati

266 Thus, CPSF6 alone controls the key molecular interactions that specify HIV-1 preintegration

267 Most DNA processes are governed by molecular interactions that take place in a sequence-spe

268 Understanding the molecular interactions that undelay these responses will

269 challenging the current understanding of the molecular interactions that underlie TDI.

270 tify additional genetic targets and specific molecular interactions that we can study and apply for t

271 tion algorithms to a network of thousands of molecular interactions to find high-confidence, interpre

272 ion and the relative contribution of diverse molecular interactions to suppressor activity.

273 hemical fragments and present all the unique molecular interactions to the target proteins with avail

274 genetic configurations significantly altered molecular interactions underlying MAPK pathway reactivat

275 studies have elucidated many aspects of the molecular interactions underlying the formation of these

276 However, the molecular interactions underlying the recruitment of com

277 we apply protein engineering to dissect the molecular interactions underlying the recruitment of thi

278 icient for AAUAAA motif recognition, yet the molecular interactions underpinning its assembly and mec

279 equilibrium measurements of a wide range of molecular interactions using a gel electrophoresis reado

280 ical translation for the importance of these molecular interactions using an imaging genetics strateg

281 tial to capture non-linear relations between molecular interactions using high-dimensional sparse dat

282 bilization is a key step involved in probing molecular interactions using single-molecule force spect

283 eriments demonstrated that Cx43-beta-tubulin molecular interaction was depleted due to protein-protei

284 The molecular interactions we see between poliovirus and its

285 The molecular interactions were characterized by Fourier tra

286 Taken together, our findings define a novel molecular interaction with the neuronal LTCC that is req

287 algorithm that integrates databases of known molecular interactions with gene expression data; such i

288 This necessitates the manipulation of molecular interactions with high precision.

289 eveloped HDNetDB, a database that integrates molecular interactions with many HD-relevant datasets.

290 d potencies, it is hypothesized that gaining molecular interactions with residues in the alpha4 and r

291 hid OBP crystal structures and examine their molecular interactions with the alarm pheromone componen

292 tional secretion of FGF2 are: (i) sequential molecular interactions with the inner leaflet along with

293 unique, and in some cases sequence-specific molecular interactions with the surface of carbon nanotu

294 e GLP-1 receptor that predict additional key molecular interactions with these amino acids.

295 rfaced nucleic acid platform for programming molecular interactions, with implications for in vivo mo

296 review recent reports of ABA-JA hormonal and molecular interactions within a physiological framework

297 properties of the cytosol implicitly govern molecular interactions within cells.

298 lication of electrical stimulus modifies the molecular interactions within the complex and consequent

299 candidate linking all these properties being molecular interactions within the peptide-loading comple

300 as been solved by X-ray crystallography, the molecular interactions within the POT1-TPP1-ssDNA ternar