ライフサイエンスコーパス: molecular complex

1 triangles (which constitutes a 30-megadalton molecular complex).

2 stabilizing effect of immobilization of the molecular complex.

3 integration of both molecules into the same molecular complex.

4 ane and its co-localization with the TCR-CD3 molecular complex.

5 RNA-containing U1-snRNP could activate this molecular complex.

6 hese proteins are members of the NMDAR super molecular complex.

7 monin-b form the core components of the UTLD molecular complex.

8 y involves a single active Galpha(olf)-ACIII molecular complex.

9 eta, Pyk2, and Lyn exist constitutively in a molecular complex.

10 cadherins are not contained within the same molecular complex.

11 r confirm three-dimensional structure of the molecular complex.

12 teract and can be co-immunoprecipitated as a molecular complex.

13 ypically work together in the same system or molecular complex.

14 arious biological processes mediated by this molecular complex.

15 distinct signaling effectors within a large molecular complex.

16 rately initiate distinct actions on a single molecular complex.

17 RII and HtrII are physically associated in a molecular complex.

18 driving forces involved in formation of the molecular complex.

19 iple intermolecular interactions in the same molecular complex.

20 ssociate further in a regular way into supra-molecular complexes.

21 dynamics and the occurrence of subresolution molecular complexes.

22 process, functioning at the level of single molecular complexes.

23 LC8 is present in various molecular complexes.

24 catalytic activities comparable to those of molecular complexes.

25 is not an effective mechanism for regulating molecular complexes.

26 cadherins are not contained within the same molecular complexes.

27 plot suggested the existence of higher order molecular complexes.

28 planetary atmospheres is extended to include molecular complexes.

29 lization of biosynthetic enzymes in discrete molecular complexes.

30 of the soft intermolecular vibrations in the molecular complexes.

31 ent of photosignaling activity of SRII-HtrII molecular complexes.

32 nabled the ordered assembly of tubular supra-molecular complexes.

33 c fields required to produce dissociation of molecular complexes.

34 ssembly of rhenium(I) bipyridine tricarbonyl molecular complexes.

35 f counting the number of subunits in example molecular complexes.

36 motes their removal from chromatin and other molecular complexes.

37 ex remains a major challenge for homogeneous molecular complexes.

38 on of these structural features in synthetic molecular complexes.

39 h population redistributions of higher-order molecular complexes.

40 ing the known tetravalent lanthanide ions in molecular complexes.

41 olymerases that are targeted to promoters by molecular complexes.

42 rates with transition metal atoms, ions, and molecular complexes.

43 mutational ratchet systematically entrenches molecular complexes.

44 APC) and effector T cells form transcellular molecular complexes.

45 both recruit SHIP, this occurs via distinct molecular complexes.

46 r species and the intrinsic heterogeneity of molecular complexes.

47 arrangements of different components within molecular complexes.

48 ncepts about manipulating properties of atom/molecular complexes.

49 avior was observed on irradiating homologous molecular complexes 1 subset2a, 1 subset2b, and 1 subset

50 l type VI secretion system (T6SS) is a supra-molecular complex akin to bacteriophage tails, with VgrG

51 ent sum of diffraction from rigid individual molecular complexes aligned along several discrete cryst

52 The bright molecular complex allowed for the fastest video-rate ima

53 Natural electrophoresis of molecular complexes allows compounds to travel through t

54 Disturbing this molecular complex alters neuronal polarity and causes st

55 torial complexity in the number of potential molecular complexes among these core components and dyna

56 mbers of the p24 family have been found in a molecular complex and are enriched in COPI-coated vesicl

57 oxyl terminus of the I(Ks) channel to form a molecular complex and control its phosphorylation state,

58 These findings correlate with an altered HTT molecular complex and distinct proteins in the HTT inter

59 hat these antigens are able to form a larger molecular complex and induce similar signals.

60 oft acid-base coordination reactions between molecular complexes and colloidal nanostructures, we sho

61 ssed, and typical examples and benchmarks on molecular complexes and crystals are provided.

62 he bioavailability of carcinogens by forming molecular complexes and enhances their elimination in th

63 The nature of a Jahn-Teller distortion in molecular complexes and extended lattices can be manipul

64 opposite sides, compact tiling of members of molecular complexes and extensively making use of nested

65 vides a way to account for all the potential molecular complexes and interactions among multivalent o

66 We describe a method to detect molecular complexes and measure their stoichiometry in l

67 rns the differences and similarities between molecular complexes and metal NPs in their reactivity to

68 the composition, regulation and function of molecular complexes and pathways have been gained.

69 Simmune Modeler that allows users to specify molecular complexes and their interactions as well as th

70 an reveal the kinetic behavior of individual molecular complexes and thus have the potential to deter

71 like MscL and MscS, may coexist in multiple molecular complexes and, consequently, have their activa

72 dynamical studies of radical intermediates, molecular complexes, and conformationally flexible molec

73 and refolding of dimeric target proteins in molecular complexes, and its interactions with selective

74 ds, and steric repulsion in small molecules, molecular complexes, and solids.

75 s, which are part of five distinct cytosolic molecular complexes: AP-3, homotypic fusion and vacuole

76 veral thousands of paramagnetic Octametallic Molecular Complexes are covalently bonded between two FM

77 amyloidoses or other diseases where abnormal molecular complexes are formed in serum.

78 Small ion-dihydrate molecular complexes are ideal systems with which to inve

79 In addition, we demonstrate that the NIR-II molecular complexes are superior to clinically approved

80 Integrin and kindlin reside in a molecular complex as soon as adhesions are visible; tali

81 In this chapter, we review the molecular complexes assembled by these proteins, the str

82 Quantifying multi-molecular complex assembly in specific cytoplasmic compa

83 rotein-protein interaction networks revealed molecular complexes associated with nitrate and light si

84 We describe a general method for detecting molecular complexes based on the analysis of single mole

85 LTA and Hb appear to form a molecular complex, based on the ability of each to affec

86 esponses often begin with the formation of a molecular complex between a T-cell receptor (TCR) and a

87 h in vivo Furthermore, we identified a novel molecular complex between FAK and Runx1 in the nucleus o

88 plaques were significantly reduced, and the molecular complex between Src, FAK, and vinculin was dis

89 The ligands are molecular complexes between antigenic peptides and prote

90 Molecular complexes between CdSe nanocrystals and Clostr

91 ts, we suggest that L-whirlin is part of the molecular complexes bridging PCDH15-, and possibly CDH23

92 me an important tool for investigating large molecular complexes by providing quantitative informatio

93 by the protease caspase-1 within a cytosolic molecular complex called the inflammasome.

94 We chose to target the inflammasome, a molecular complex capable of detecting infection and cel

95 These results suggest that a molecular complex composed of Nde1, Lis1, and Brap regul

96 oked a marked increase in the formation of a molecular complex composed of TRAF6 and beta-arrestin-2.

97 Photoirradiation of a hydrogen-bonded molecular complex comprising acyclic components, namely,

98 These results demonstrate a unique molecular complex comprising CXCR4, FAK, ASK1, and PP5 i

99 ts and transfected 293 cells, we find that a molecular complex comprising Src, Pyk2, and Cbl function

100 show the first experimental evidence that a molecular complex consisting of a DNA template and assoc

101 Ab, KP15, directed against the MHC-I/peptide molecular complex consisting of H-2D(d) and a decamer pe

102 tructure to form a combining site, recognize molecular complexes consisting of peptides bound to MHC

103 fluorescence complementation to visualize a molecular complex containing a Mig-10/RIAM/lamellipodin

104 x, which subsequently recruited an autophagy molecular complex containing Beclin1 and Bif-1 to the li

105 t/Itk SH2 domain mediates the formation of a molecular complex containing Emt/Itk, LAT, and TCR/CD3;

106 hesions and subsequent cell activation via a molecular complex containing FAK, ZAP-70, and paxillin.

107 The molecular complex containing the phototaxis receptor sen

108 The molecular complexes containing CARMA proteins have been

109 ed to the cell periphery and associated with molecular complexes containing phosphorylated Pyk2, sugg

110 temperatures found on planetary atmospheres, molecular complexes contribute to both atmospheric chemi

111 Thus, unique molecular complexes control kinase and phosphatase activ

112 ion in translational control of mRNAs within molecular complexes dedicated to cell-cycle progression,

113 o infer not only model parameters describing molecular complexes, e.g., rate constants, but also info

114 s the first direct comparison of enzymes and molecular complexes, enabling a unique understanding of

115 Furthermore this molecular complex exhibits a biased migration into a con

116 and LRP and CRT are associated with hep I in molecular complexes extracted from cells.

117 The ATP-sensitive potassium channel is a key molecular complex for glucose-stimulated insulin secreti

118 he design principle can be extended to other molecular complexes for in vivo studies.

119 d leads to one of the most active and robust molecular complexes for water oxidation at neutral pH wi

120 and temporal resolution, "when" and "where" molecular complexes form and their stoichiometry in nasc

121 The hetero-molecular complex formation prevents IAPP from self-asso

122 edicted to be unstructured in the absence of molecular complex formation, suggesting that the interac

123 rylation dependent fashion, in a 100-200-kDa molecular complex formation.

124 Our data reveal that a molecular complex formed by MG53, dysferlin, and Cav3 is

125 A trinuclear T-shaped nickel thiolate molecular complex has been designed to activate dinitrog

126 All the steps leading to the final grafted molecular complex have been identified by DFT.

127 rrent bonding paradigms, two terminal Au-oxo molecular complexes have been synthesized by reaction of

128 cently, however, porous hybrid metal-organic molecular complexes have received considerable attention

129 e environments discussed are very different, molecular complexes have recently been considered as pot

130 Cocrystals are molecular complexes having crystal structures different

131 phering the specific spatial organization of molecular complexes hidden in dense multi-color super-re

132 Here, we show that a molecular complex identified in Drosophila epidermal dif

133 Encapsulation of a biological molecule or a molecular complex in a vesicle provides a means of biofr

134 causes divergence of one element of a supra-molecular complex in order to maintain the function of t

135 ociation energy (D0) of an isolated and cold molecular complex in the gas-phase is a fundamental meas

136 othesize that M6CK associates with the PRMT5 molecular complex in the nucleus, directing M6CK to a sp

137 onstrate that PARP and Ku autoantigen form a molecular complex in vivo and in vitro in the absence of

138 inal threonine residue within a kinase-ezrin molecular complex in vivo.

139 nstrate that TbORC1/CDC6 interacts in a high molecular complex in which a diverged Orc4 homologue and

140 atory, and theoretical database, the role of molecular complexes in close and far away is discussed.

141 nd reveal previously unknown PLVAP-dependent molecular complexes in LSEC during angiogenesis.

142 lation analyses and robust quantification of molecular complexes in multiplexed super-resolution micr

143 Structures of molecular complexes in the disciplines of immunology and

144 ly attributed to tetraspanins is to organize molecular complexes in the plasma membrane by using mult

145 rate when using 3D template matching to find molecular complexes in tomograms.

146 detection but also for structural mapping of molecular complexes in which individual components are t

147 previous studies on the backbone dynamics of molecular complexes in which reduced mobilities were typ

148 lays a central role, through a GRB2-mediated molecular complex, in fear memory formation in the later

149 n/dynactin adaptor Bicaudal D-1 (Bicd1) in a molecular complex including the dynactin subunit dynacti

150 Molecular complexes including vigilin comprise proteins

151 vity is modulated by partner proteins in its molecular complex, including the MCUb subunit.

152 This molecular complex increased the monoubiquitination of hi

153 Typically, molecular complexes interact via "slip bonds," so applie

154 s used to study F-actin, a large filamentous molecular complex involved in many cellular functions.

155 clear RNA is a highly conserved intranuclear molecular complex involved in splicing pre-mRNA.

156 In the presence of antigen, a molecular complex is formed where the cleavable linkage

157 In dynamic force spectroscopy, a (bio-)molecular complex is subjected to a steadily increasing

158 sence of Tax, expression of the hTid-1/Hsp70 molecular complex is targeted to perinuclear mitochondri

159 Oxidation of ammonia by molecular complexes is a burgeoning area of research, wi

160 The power of FRET to study molecular complexes is expanded by the use of two or mor

161 ing since the association of PI 3-kinases in molecular complexes is not necessarily correlated with t

162 In addition, in the case of weakly bound molecular complexes, it is usual to observe the effects

163 e shown that caspase-2 activation requires a molecular complex known as the PIDDosome comprising the

164 Large molecular complexes known as inflammasomes regulate the

165 Several types of materials, namely resins, molecular complexes, layered double hydroxides, and pure

166 A molecular complex, LCZ696, developed by scientists at No

167 e scaffolding functions of PRX and AHNAK2 in molecular complexes linking the extracellular matrix to

168 photomagnetic linker yielded the trinuclear molecular complex [{Mn(saltmen)}2FeHS(LN5)(CN)2](ClO4)2.

169 Amphibian IFNs represent a molecular complex more complicated than those in other v

170 PRX participates in large molecular complexes, most likely through the interaction

171 and regulates crucial cell functions via the molecular complexes mTORC1 and mTORC2.

172 All three components of the tri-molecular complex must be present to preserve normal MMP

173 pproach can we assess the oligomeric state a molecular complex must form in order to regulate a compl

174 dual actin filaments and lateral movement of molecular complexes must all be incorporated to correctl

175 In molecular complexes, nitride coupling has been observed

176 8-fold activity enhancement, compared to the molecular complex of Cu with an identical coordination s

177 Here we report a molecular complex of iron (an abundant and inexpensive m

178 ule regulating AP-1 activity by organizing a molecular complex of kinases and transcription factors,

179 at the cell surface induce the assembly of a molecular complex of NCAM140, p125(fak), and p59(fyn) an

180 n G1 promoter element, tethered cdx-2 to the molecular complex of pax-6 and p300.

181 ISMMC consist of a molecular complex of polyosome/ribosome-bound ubiquitina

182 ion of MMP-2 requires the formation of a tri-molecular complex of pro-MMP-2, MMP-14, and tissue inhib

183 lasmic Ca(2+) homeostasis and organizing the molecular complex of the triad but not in regulating ske

184 tion of pax-6 with p300, thus establishing a molecular complex of transcription factors implicated in

185 he intermolecular short hydrogen bond in the molecular complex of urea and phosphoric acid are invest

186 Helper T cells are triggered by molecular complexes of antigenic peptides and class II p

187 el that implies the cooperative formation of molecular complexes of dihydrocholesterol and phospholip

188 Synthetic strategies to yield molecular complexes of high-valent lanthanides, other th

189 The first molecular complexes of holmium and erbium in the +2 oxid

190 Out of the 14 lanthanide (Ln) ions, molecular complexes of Ln(IV) were known only for cerium

191 of mGFP-hDAT co-exist and that higher-order molecular complexes of mGFP-hDAT are absent at the plasm

192 he SPM domain in the assembly or function of molecular complexes of PcG proteins.

193 e multiply bound "oxo"-type ligands found in molecular complexes of Pu(V) and Pu(VI); (3) the Pu asso

194 ectroscopy is used to detect hydrogen-bonded molecular complexes of pyridine with water in the near f

195 A binuclear manganese molecular complex [(OH2)(terpy)Mn(mu-O)2Mn(terpy)(OH2)](

196 microscopy revealed individual steps of the molecular complex on its diffusion pathway, with increas

197 influences T cell function we evaluated CD81 molecular complexes on T cells.

198 They function as transiently assembled molecular complexes on the membrane, and their disassemb

199 Initial formation of a tri-molecular complex (one 'free' IgE molecule cross-linking

200 nsensus as to either the nature of the toxic molecular complex or the mechanism by which toxic aggreg

201 e, and the operon's gene products often form molecular complexes or metabolic pathways.

202 The assembly of this tri-molecular complex permits the activated Rho-family GTPas

203 f this protein appears to be due to distinct molecular complexes, possibly related to differential gl

204 Benzene reduction by molecular complexes remains an important synthetic chall

205 We propose that formation of a TNFR1-ARTS-1 molecular complex represents a novel mechanism by which

206 oded by the Usher syndrome type 1 genes form molecular complexes required for hair-bundle development

207 in the formation of active 45-kDa and 55-kDa molecular complexes, respectively.

208 Crystal structures of the three molecular complexes revealed that IST1 binds to the MIT

209 A molecular complex scaffolded by the GK protein-interacti

210 imaging technology with single-molecule (or molecular-complex) sensitivity, together with refinement

211 Molecular complexes, solid-state Haber-Bosch catalytic s

212 can reveal the structural details of stable molecular complexes, strategies must be developed to cha

213 des) to properly draw cellular locations and molecular complex structures.

214 By verifying the functional state of each molecular complex studied, we could exclude models in wh

215 sessing the integrity and stability of large molecular complexes such as the proteasome, we detect an

216 iched for metabolic processes carried out by molecular complexes such as the ribosome.

217 number of fluorescent units in subresolution molecular complexes, such as in toxic protein oligomers

218 characterized by a central cluster of BCR/Ag molecular complexes surrounded by a ring of LFA-1/ICAM-1

219 ncept that activation of the inflammasome, a molecular complex that activates caspase-1 and in turn t

220 agments and is RAS-specific, producing a tri-molecular complex that auto-activates the caspase pathwa

221 A molecular complex that can mediate an N(2) reduction cyc

222 The ribosome is a large molecular complex that consists of at least three ribonu

223 s for GR, YB-1, and UK in the formation of a molecular complex that degrades MCP-1 mRNA.

224 nectin, fibulin-1, and SOF form a quaternary molecular complex that enhanced the binding of fibulin-1

225 ed beta-catenin to dnTCF-1 to form a ternary molecular complex that enhanced Wnt/beta-catenin signali

226 in mechanotransduction, as a component of a molecular complex that functions only in the setting of

227 at beta-arrestin 1 recruited Src kinase to a molecular complex that included the ETA receptor.

228 us facilitates formation of the "pre-TCR," a molecular complex that is important for the subsequent d

229 Cyclin L2 and SAMHD1 form a molecular complex that is partially dependent on the pre

230 lton (OIP106/GRIF1) proteins, members of the molecular complex that links mitochondria to kinesin mot

231 protein arginine methyltransferase 5 (PRMT5) molecular complex that make important epigenetic modific

232 Mediator is a multi-unit molecular complex that plays a key role in transferring

233 -2) and its signaling counterpart DAP12 as a molecular complex that promotes phagocytosis of bacteria

234 sembly and forms part of a poorly understood molecular complex that remains associated with growing f

235 in a companion paper for an IL-7-associated molecular complex that selectively stimulates the prolif

236 , and LIF receptor (LIFR) and STAT4 formed a molecular complex that, together with JAK1 and TYK2 kina

237 This memory depends on molecular complexes that are highly conserved among euka

238 apable of studying the motions of very large molecular complexes that are otherwise completely beyond

239 dimerization of Ret/ptc2 allows assembly of molecular complexes that are properly localized via Enig

240 d for structure determination of abiological molecular complexes that arise in an aggregate state.

241 e lagging strand template, and they identify molecular complexes that can be further examined by stru

242 s crucially dependent on the mobility of the molecular complexes that catalyze the conversion of sunl

243 he presence of BIG1 and nucleolin in dynamic molecular complexes that change in composition while mov

244 he presenilins (PSs) are components of large molecular complexes that contain beta-catenin and functi

245 lecule acts as an organizer of submembranous molecular complexes that control the coordinated actin p

246 ll adhesion molecules form membrane-spanning molecular complexes that couple homophilic binding by th

247 cell polarity and participates in different molecular complexes that define apical and lateral membr

248 prin-alpha2 promotes dynamic scaffolding for molecular complexes that facilitate synaptic vesicle rel

249 ntributor to this balance is the behavior of molecular complexes that function in various regulatory

250 sensory dendrites M10s belong to large multi-molecular complexes that include pheromone receptors and

251 ide of focal adhesions is comprised of large molecular complexes that link transmembrane receptors, s

252 TRIP8b as well as for proper assembly of the molecular complexes that mediate the effects of TRIP8b o

253 Although molecular complexes that mediate these interactions in t

254 ificant progress has been made in developing molecular complexes that reduce N(2) into its bioavailab

255 the role of FAK as a scaffolding protein in molecular complexes that regulate gene transcription.

256 Cage-like molecular complexes that self-assemble through weak inte

257 Inflammasomes are cytosolic multi-molecular complexes that sense intracellular microbial d

258 eoid near the cell center, whereas ribosomes-molecular complexes that translate mRNAs into proteins-a

259 d directly measure electronic couplings in a molecular complex, the Fenna-Matthews-Olson photosynthet

260 ar signaling, the assembly and regulation of molecular complexes, the mechanisms through which mutati

261 ich are Crohn's disease risk factors, form a molecular complex to modulate autophagic responses to mi

262 membrane where they function within multiple molecular complexes to contribute to the establishment a

263 distinct functions and act in three separate molecular complexes to promote mitochondrial fusion.

264 air of essential cofactors in a higher-order molecular complex, to mediate its transcriptional effect

265 m across all scales-from their molecules, to molecular complexes, to organelles.

266 pitation analyses revealed that TrkA forms a molecular complex together with either full-length p75 o

267 ght the evolutionary plasticity of conserved molecular complexes under the constraints of essential g

268 ociated membrane protein [VAMP]) forming the molecular complex underlying neurosecretion.

269 ers consisting of the magnitude and phase of molecular complex-valued chiral susceptibility ratio, re

270 ypes can be assembled, independently, into a molecular complex via a protein-protein interaction (PPI

271 were misfolded and formed aggregates or high molecular complexes via disulfide bonds.

272 e sagA mutant strains are unable to form the molecular complexes which are needed to keep the cells i

273 d output elements in the same self-assembled molecular complex, which reduces diffusion-mediated sign

274 quantitative predictions on the abundance of molecular complexes while performing the best qualitativ

275 on using a colloidal nanographene to form a molecular complex with a metal ion to tackle this challe

276 SRI exists in the membrane as a molecular complex with a signal transducer protein.

277 acts by binding to P2X receptors that form a molecular complex with ASICs; the receptor on sensory ne

278 t the protein phosphatase 2A (PP2A) was in a molecular complex with beta-arrestin1 and that the PP2A

279 ging microscopy, PKCalpha is shown to form a molecular complex with ezrin, and the PKC-co-precipitate

280 of AF-1 through the formation of a true tri-molecular complex with JunD dimers and DNA that assemble

281 gent on its partner's history and allowing a molecular complex with novel specificity to evolve.

282 NrCAM formed a molecular complex with Npn-2 in brain and neural cells,

283 tic vesicles of sympathetic neurons, forms a molecular complex with proteins of the vesicular fusion

284 found that HDAC6 forms a previously unknown molecular complex with STAT3, association that was detec

285 the solid state, rather, the product 10 is a molecular complex with strong hydrogen bonds between eac

286 Furthermore, kindlerin is recruited into a molecular complex with the beta1A and beta3 integrin cyt

287 and 2) beta-arrestin 1 and Src kinase form a molecular complex with the ETA receptor to mediate ET-1

288 ults demonstrate that Galpha13SR2 forms a bi-molecular complex with the head domain of talin and ther

289 ther with the zinc fingers, forms a cohesive molecular complex with the nucleic acid.

290 Pto resides in a constitutive molecular complex with the nucleotide binding site-leuci

291 d-mediated activation allows EphA2 to form a molecular complex with the SHC and GRB2 adaptor proteins

292 usly to the VEGF promoter, where they form a molecular complex with the transcription coactivators CB

293 ed distal C-terminal domain forms a specific molecular complex with the truncated alpha(1) subunit an

294 It is able to form molecular complexes with different DNA targets and also

295 Furthermore, we show that flotillins form molecular complexes with EGFR in an EGF/EGFR kinase-inde

296 ractome network maps contain several hundred molecular complexes with limited and somewhat controvers

297 imaging technique with capability to detect molecular complexes with near angstrom resolution, to es

298 aptic vesicles of sympathetic neurons, forms molecular complexes with the synaptic vesicle proteins s

299 ins collaboratively bind DNA as higher-order molecular complexes with unknown consequences for mammal

300 y imaging the organization of organelles and molecular complexes, with recent applications increasing