ライフサイエンスコーパス: molecular complex

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

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

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

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

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

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

7 cadherins are not contained within the same molecular complex.

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

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

10 arious biological processes mediated by this molecular complex.

11 distinct signaling effectors within a large molecular complex.

12 rately initiate distinct actions on a single molecular complex.

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

14 driving forces involved in formation of the molecular complex.

15 iple intermolecular interactions in the same molecular complex.

16 stabilizing effect of immobilization of the molecular complex.

17 integration of both molecules into the same molecular complex.

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

19 is not an effective mechanism for regulating molecular complexes.

20 cadherins are not contained within the same molecular complexes.

21 plot suggested the existence of higher order molecular complexes.

22 planetary atmospheres is extended to include molecular complexes.

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

24 lization of biosynthetic enzymes in discrete molecular complexes.

25 of the soft intermolecular vibrations in the molecular complexes.

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

27 c fields required to produce dissociation of molecular complexes.

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

29 r species and the intrinsic heterogeneity of molecular complexes.

30 arrangements of different components within molecular complexes.

31 ncepts about manipulating properties of atom/molecular complexes.

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

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

34 LC8 is present in various molecular complexes.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

64 Quantifying multi-molecular complex assembly in specific cytoplasmic compa

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

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

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

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

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

70 The ligands are molecular complexes between antigenic peptides and prote

71 Molecular complexes between CdSe nanocrystals and Clostr

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

87 The molecular complex containing the phototaxis receptor sen

88 The molecular complexes containing CARMA proteins have been

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

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

91 Thus, unique molecular complexes control kinase and phosphatase activ

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

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

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

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

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

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

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

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

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

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

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

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

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

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

106 Cocrystals are molecular complexes having crystal structures different

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

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

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

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

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

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

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

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

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

116 Structures of molecular complexes in the disciplines of immunology and

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

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

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

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

121 Molecular complexes including vigilin comprise proteins

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

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

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

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

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

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

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

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

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

131 Large molecular complexes known as inflammasomes regulate the

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

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

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

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

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

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

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

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

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

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

142 In molecular complexes, nitride coupling has been observed

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

169 A molecular complex scaffolded by the GK protein-interacti

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

208 Although molecular complexes that mediate these interactions in t

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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