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1 ertoire of Lon substrates to be tuned by its assembly state.
2 latory mechanisms in controlling kinetochore assembly state.
3 ative electrophoresis (BNE) to study GluA1-3 assembly state.
4 eptors shows a strong dependence on the TMVP assembly state.
5 idual pigment sites as a function of protein assembly state.
6 the coupling of molecular interactions with assembly state.
7 ciliogenesis, tubulin synthesis, and tubulin assembly state.
8 basis of aggregation of Abeta into distinct assembly states.
9 neurodegenerative diseases exist in diverse assembly states.
10 does not induce the formation of additional assembly states.
15 iate filaments (IF) is known to affect their assembly state and organization; however, little is know
16 ng the transition from dimeric to tetrameric assembly states and, second, at a postassembly trafficki
17 exhibited purification behavior, CD spectra, assembly state, and inducer binding properties similar t
18 examined the equilibrium folding properties, assembly states, and stabilities of the early folding st
19 valence of intermediate and large oligomeric assembly states are associated with both ageing and Alzh
21 sitions through different conformational and assembly states as it matures into a functional helicase
22 gulation is morphogenetically coupled to the assembly state by control of the anti-sigma factor FlgM.
23 tamer is a physiological, stable, and active assembly state capable of forming lethal toxins that may
24 abeled MNP monitored non-invasively based on assembly state-dependent changes in the emission spectru
25 ch represent the features of an intermediate assembly state during maturation, the SP1 peptide exists
27 ons was performed to compare the microtubule assembly state in neurons of diseased and control cases
30 onassociating species or as a combination of assembly states independent of protein concentration.
31 osterically regulated by the transmission of assembly-state information from the C-terminal domain, w
32 iological alpha-syn conformers into compact, assembly-state intermediates by glucosylceramide (GluCer
33 ore dynamic than previously reported and its assembly state is sensitive to stimuli that alter cellul
34 ly, the relative population of the different assembly states is determined via a Bayesian-based Monte
35 st, a basis set comprising a small number of assembly states is generated from extensive CG simulatio
36 ows that resistin circulates in two distinct assembly states, likely corresponding to hexamers and tr
42 cate that, in addition to lipid content, the assembly state of apoE influences Abeta binding and rece
43 t studies have shown that the lipidation and assembly state of apolipoprotein E (apoE) determine rece
44 otide analogues, we have also correlated the assembly state of ClpA in the presence of these nucleoti
45 lytical ultracentrifugation to determine the assembly state of CVX in solution and surface plasmon re
48 r spatiotemporal expression and the physical assembly state of fibronectin (FN) matrix play key roles
50 larity of migrating cells by controlling the assembly state of NMII-A, its cellular localization, and
51 en together, these data demonstrate that the assembly state of peroxisomal proteins and the chaperone
54 self and foreign epitopes regardless of the assembly state of the antigen, suggesting that conjugati
56 ochemical studies conflict on the oligomeric assembly state of the protease complex, and its detailed
58 ontrol cardiolipin metabolism and affect the assembly state of TIM23 and its association with PAM in
59 mine the effects of nestin expression on the assembly state of vimentin IFs in nestin-free cells.
63 simulations is developed to characterize the assembly states of Hck, a member of the Src-family kinas
64 spectrometry experiments characterizing the assembly states of intact NtrC4 (a sigma(54) activator f
67 ternary structure occurs via changes in self-assembly state or through the gain or loss of protein su
69 pramolecular structures were compared to the assembly states predicted by packing constraints that we
71 rbed, whereby a decrease in the III(2)-IV(2) assembly state relative to the III(2)-IV form is observe
74 ion of the full repertoire of conformers and assembly states that can be accessed by PrP under specif
75 otides in the bI3 group I intron RNP in four assembly states: the free RNA, maturase-bound RNA, Mrs1-
76 nance biosensor analysis to characterize the assembly state, thermodynamics, and kinetics of the CD4-
77 and Abeta42 have different conformations and assembly states upon refolding from their unfolded ensem
78 rent shifts in the equilibrium population of assembly states upon the binding of different signaling
79 , stability, and dynamics of P8 in different assembly states using time-resolved Raman spectroscopy a
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