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1 interactions allow MuSK not only to induce a multimolecular AChR-containing complex, but also to loca
2 ce that FcalphaR-mediated signals modulate a multimolecular adaptor protein complex containing Grb2,
3 ates to cytoplasmic stress granules that are multimolecular aggregates of stalled translation initiat
4  provides an optical platform to develop new multimolecular and functional imaging capabilities.
5                      HDL encompasses dynamic multimolecular and multifunctional lipoproteins that lik
6 y in conveying explicit signals across large multimolecular assemblies and distances to specify cellu
7 n water to form different kinds of nanoscale multimolecular assemblies ranging from simple micelles a
8 KAP) sequences that can act as scaffolds for multimolecular assemblies that facilitate and limit cAMP
9 s, can function as integral members of large multimolecular assemblies, and are self-regulating.
10 l molecules are designed to come together in multimolecular assemblies, such as in coordination cages
11 ociates with p300, suggesting a mechanism of multimolecular assembly at the +6.1 kb site.
12   ERK1/2 co-immunoprecipitated with Akt in a multimolecular assembly of signaling molecules, containi
13 insen cage" whose primary role is to prevent multimolecular association during folding.
14 involves the formation of a ligand-dependent multimolecular association of receptor chains (alpha and
15  that the difference is caused by reversible multimolecular association while folding in solution, an
16                           By applying pulsed multimolecular beam experiments and in situ infrared ref
17 analysis and machine learning has identified multimolecular biomarker panels.
18 d that RyR2 and CASQ2 interact as parts of a multimolecular Ca(2+)-signaling complex; however, direct
19                                              Multimolecular caps appeared within minutes of B7-DC XAb
20 pathway initiation complexes are composed of multimolecular carbohydrate recognition subcomponents an
21  about the rules that guide the formation of multimolecular chromatin-bound complexes have helped to
22 lexes on the surface of human fibroblasts in multimolecular clusters unassociated with coated pits, a
23 ized red blood cells support the assembly of multimolecular coagulation complexes.
24 Mango III) and the creation of an artificial multimolecular communication pathway between Cas12a and
25 and repair factors, could assemble to form a multimolecular complex ("mutasome") at the site of DNA l
26                 ProMMP-2 activation requires multimolecular complex assembly involving proMMP-2, memb
27 crophage cytosol activates a host-protective multimolecular complex called the inflammasome to releas
28      We demonstrated that the formation of a multimolecular complex comprised of AR/beta(1) Pix/STUB1
29 ata indicate that a significant portion of a multimolecular complex containing Cbl, SLP-76, Shc, and
30 ting expression of PTPmu and by organizing a multimolecular complex containing PKCbetaII, RACK1, PTPm
31 CT molecules in a temporal fashion to form a multimolecular complex during the early stages of endoth
32 ssium conductance and spatial buffering, and multimolecular complex dynamics, and indicate both estab
33  cognate interactions by, e.g. affecting TCR-multimolecular complex formation and antigen binding aff
34              The activation process requires multimolecular complex formation involving pro-MMP-2, me
35 eginnings and the AR increase is part of the multimolecular complex including downstream effector pro
36 ed that the presence of a specific pRb2/p130 multimolecular complex on the ER-alpha promoter strongly
37 kinase activity, (iv) activation of Sos in a multimolecular complex that contains p46Shc, and p52Shc,
38                       The hemidesmosome is a multimolecular complex that integrates the extracellular
39 e dystrophin glycoprotein complex (DGC) is a multimolecular complex that links the extracellular matr
40                        CAS is thus part of a multimolecular complex that, along with other cadherin-b
41 nt phosphorylation of multiple proteins in a multimolecular complex with attendant modulation of thei
42   Moreover, we demonstrate that TLR9 forms a multimolecular complex with gp96 and CNPY3, and the bind
43  binds to HSP90 and disrupts the Raf-1-HSP90 multimolecular complex, leading to destabilization of Ra
44 thway in which five proteins assemble into a multimolecular complex, the membrane attack complex (MAC
45 antigenic sites and neighboring Ags within a multimolecular complex.
46 on of a connexin domain when integrated in a multimolecular complex.
47 ity is analogous to cooperativity in another multimolecular complex: hemoglobin.
48 r CD8(+) cells named self-immune stimulatory multimolecular complexes (ISMMC).
49 UFH, LMWH, 16-, 8-, 6-mer), (2) formation of multimolecular complexes (UFH, 16-, 8-mer), and (3) ener
50                 Cx36 gap junctions represent multimolecular complexes and contain cytoskeletal, regul
51 ore mechanisms governing dynamic assembly of multimolecular complexes and their role in shaping cellu
52 ndothelium; 2) whether they are organized in multimolecular complexes as in neurons; and 3) whether t
53          We have previously shown that PF4:H multimolecular complexes assemble through electrostatic
54  or that they function as mutually exclusive multimolecular complexes by providing direct support for
55        These findings suggest that pRb2/p130-multimolecular complexes can be key elements in the regu
56                         They are enriched in multimolecular complexes composed of voltage-gated Nav a
57 s in neurons; and 3) whether the endothelial multimolecular complexes differ from their neuronal coun
58          In this report, we investigated the multimolecular complexes formed following anti-Ig stimul
59 oth macroscopic visible aggregates and small multimolecular complexes in solution are capable of indu
60  Current concepts favour their assembly into multimolecular complexes in the plasma membrane in respo
61 of ER-alpha chromatin structure by pRb2/p130 multimolecular complexes may influence its susceptibilit
62 imulations show that cooperative assembly of multimolecular complexes nucleated by activated receptor
63 openia is initiated by and directed to large multimolecular complexes of platelet factor 4 (PF4) and
64 ed by platelet-activating antibodies against multimolecular complexes of platelet factor 4 and hepari
65 ciated proteins could direct the assembly of multimolecular complexes on leukocyte microvilli.
66 facilitate signal transduction by preforming multimolecular complexes that can be rapidly activated b
67 ively charged compounds through formation of multimolecular complexes that lead to dendritic cell act
68 e presence of both BIG1 and KANK1 in dynamic multimolecular complexes that maintain Golgi/MTOC orient
69 etraspanins are membrane molecules that form multimolecular complexes with a broad array of molecules
70          Many autoantigens are components of multimolecular complexes, and some of the other componen
71 gesting that it may be part of two different multimolecular complexes.
72 lyses, showed that FoxP3 existed in distinct multimolecular complexes.
73 and are relevant to studying a wide range of multimolecular complexes.
74 or protein, and that mediate the assembly of multimolecular complexes.
75 ng molecules that coordinate the assembly of multimolecular complexes.
76                     It is also not clear how multimolecular DNA toroids and rods interconvert in solu
77 appropriate when the overall compositions of multimolecular ensembles are of greater importance than
78 at end conversion is an emergent property of multimolecular ensembles of microtubule wall-binding pro
79 the transmitter-release mechanism exist as a multimolecular entity and that this interaction has func
80 ide that spontaneously self-assembles into a multimolecular fibrillar architecture to drive the coass
81          Several new pairs were applied in a multimolecular FRET based sensor for detecting activatio
82                                              Multimolecular G-quadruplex formation is influenced by r
83 )(n), which we associate to the formation of multimolecular G-quadruplexes (mG4s) by using a range of
84                                      Because multimolecular G-quadruplexes are enhanced by repeat len
85 n form protein-free condensates sustained by multimolecular G-quadruplexes, highlighting their potent
86 s study we show that Ca(v)beta subunits form multimolecular homo- and heterooligomeric complexes in h
87  the elements in the basement membrane via a multimolecular junction called the hemidesmosome.
88                               Recent work on multimolecular lipid structures suggests a critical role
89 gher eukaryotes; they function together as a multimolecular machine that assembles quasinative CCT-ge
90 on is the result of the integrated action of multimolecular machineries.
91    We propose that PON is one component of a multimolecular machinery that localizes Numb by respondi
92                                Podosomes are multimolecular mechanosensory assemblies that coordinate
93 on target cells to mediate effects; (ii) the multimolecular membrane attack complex generated from th
94 to facilitate the organization of functional multimolecular membrane complexes.
95                  The dystrophin complex is a multimolecular membrane-associated protein complex whose
96 ly, organization, and efficient operation of multimolecular myosin phosphatase complexes that include
97 ses drive inflammation via activation of the multimolecular NLRP3-inflammasome complex.
98 ted during organogenesis and participates in multimolecular nuclear condensates essential for the fac
99 cular bond, or a consequence of more complex multimolecular or cellular responses, remains unclear.
100 current spikes corresponding to detection of multimolecular packets secreted by exocytosis.
101 GGCCCC)n RNA forms extremely stable uni- and multimolecular parallel G-quadruplex structures (up to 9
102 n (Ag) processing requires the action of the multimolecular peptide-loading complex within the endopl
103                                              Multimolecular phenotyping demonstrates that the molecul
104 ntracellular "molecular sensor" that forms a multimolecular platform, the NLRP3 inflammasome, which l
105 ces the formation of focal adhesion plaques, multimolecular platforms for second-phase insulin releas
106 duction, silence transcription, and regulate multimolecular protein assembly.
107 ed with folding nascent proteins, assembling multimolecular protein complexes and degrading cytosolic
108                                              Multimolecular protein complexes are important for many
109 he activity of interleukin-1 is regulated by multimolecular protein complexes called inflammasomes.
110 aracterize the large, dynamic, heterogeneous multimolecular protein complexes formed.
111 ms leading to the activation of cytoplasmic, multimolecular protein complexes, termed "inflammasomes,
112                           The formation of a multimolecular proximal signaling complex nucleated by t
113 alone is insufficient to predict whether the multimolecular racemate will or will not segregate.
114  SIM promotes association of B-arr2 with the multimolecular RanBP2/RanGAP1-SUMO nucleocytoplasmic tra
115 igin of dielectric response at the molecular/multimolecular scale.
116 m other surface immunoreceptors, making them multimolecular sensors of cellular stress.
117 ediates spreading through the formation of a multimolecular signaling complex at the cell surface tha
118 thermore, we observe that murine KSR forms a multimolecular signaling complex in human embryonic kidn
119                           JAM-A is part of a multimolecular signaling complex in which tetraspanins C
120 orm of protein kinase C (eye-PKC) comprise a multimolecular signaling complex via their interaction w
121 ation because of its association with AKAP18 multimolecular signaling complexes and suggest that targ
122 ubstrate of ZAP-70 that mediates assembly of multimolecular signaling complexes at the plasma membran
123 ause of the formation of discrete, localized multimolecular signaling complexes by A-kinase anchoring
124      Cytokines trigger the rapid assembly of multimolecular signaling complexes that direct the activ
125 n as a molecular scaffold in the assembly of multimolecular signaling complexes.
126 ed uptake likely involves the formation of a multimolecular signalling complex involving FcgammaR lea
127 arget cells by gammadelta T cells required a multimolecular stress signature composed of EPCR and cos
128 anolamine, Salmonella enterica synthesizes a multimolecular structure that mimics the carboxysome use
129            Signalling complexes are dynamic, multimolecular structures and sites for intracellular si
130            Radial spokes (RSs) are conserved multimolecular structures attached to the axonemal micro
131 rge from interactions among highly organized multimolecular structures embedded into complex and freq
132 s, 14 of which are on components of the same multimolecular T-cell receptor complex.
133 leoplasmic concentrations and/or assembly of multimolecular transcription regulatory complexes, which

 
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