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1 , the fingers were placed in three levels of splay.
2 es formed around the ATPases BRAHMA (BRM) or SPLAYED.
3 s in both orientations when the fingers were splayed.
4 us faecalis Cas1-Cas2 selectively binds to a splayed 30-base-pair prespacer bearing 4-nucleotide 3' o
6 aging in bipolar swimming in regions of pure splay and bend but switching to unipolar swimming in mix
7 es place on the area above electrodes due to splay and bend deformations of nematic liquid crystal al
10 o liquid crystalline deformations with bend, splay and twist; an analogy to cis/trans isomerism in or
12 he distal tyrosinated microtubules were less splayed and were closer to the leading edges of the grow
13 gene defect responsible for heterochromatic splaying and developmental abnormalities maps to chromos
15 of the molecule, but here the alpha-helices splay apart and are stabilized by the formation of a tai
22 ating that occurs by bundle crossing and the splaying apart of pore-lining helices commanding ion pas
23 their hand in two postures, with the fingers splayed (Apart posture) or pressed together (Together po
26 e C62-A63 step at the cleavage site adopts a splayed-apart orientation, with flexible C62 directed ou
27 antly in the alignment at the cleavage step (splayed-apart vs. base-stacked) and surrounding residues
31 ipid interface, to calculate lipid tilts and splays, as well as to fit the corresponding distribution
32 in an unusual conformation in which they are splayed at an oblique angle to each other, suggesting th
33 atin regulators: the well-studied BRAHMA and SPLAYED ATPases, as well as two closely related non-cano
36 he resultant strong suppression of twist and splay but not bend deformation in the columnar phase, ca
39 e on Fe and valency of S, and both exhibit a splayed configuration with respect to their three mu2S a
41 l C-terminal extension of TetM with a unique splayed conformation of nucleotides A1492 and A1493 at t
43 tween the last stacked base and its adjacent splayed counterpart, and positioned within the groove of
45 w that the requirement for generating saddle-splay curvature implies that a decrease in arginine cont
48 marginally stable against spontaneous saddle splay deformation, which is incompatible with long-range
49 small twist elastic moduli relieve bend and splay deformations by introducing twist deformations.
50 ositional features, such as a sandy crevasse-splay deposit are found further away from the breach.
54 unit distance (away from the inclusion), the splay-distortion component dominates close to the bilaye
55 nts: a compression-expansion component and a splay-distortion component, which includes the consequen
57 kness, the bilayer compression-expansion and splay-distortion moduli, and the inclusion radius (this
59 substrate was cleaved 90-fold faster than a splayed duplex substrate containing a single to double s
62 and render the intracellular vestibule less splayed during channel opening in the presence of ATP.
64 e spontaneous twist, we determine the saddle-splay elastic constant for chromonic liquid crystals for
65 asuring M, the ratio of the Gaussian (saddle splay) elastic modulus to the bending elastic modulus of
67 r toroidal droplets, we find that the saddle-splay energy screens the twisting energy, resulting in a
71 her than that of the L(d) phase and a saddle-splay (Gauss) modulus difference with the Gauss modulus
72 ilayers is sensitive to kappa(m), the saddle splay (Gaussian curvature) elastic modulus of the lipid
73 his is the first determination of the saddle splay (Gaussian) modulus in a lipid system consisting on
74 niform, i.e., to be locally bouquet-like or "splayed." However, it is impossible to achieve splay of
76 de supporting evidence for the presence of a splay in the G(4)-C(9) base pair of the EcoRI binding si
78 of cochlear hair cells are disorganized and splayed in mutant mice, with subsequent degeneration of
80 s develop abnormally and remain immature and splayed into adulthood, corresponding with the early ons
81 , 12-13-nm-wide filaments and filaments that splayed into two 20-25-nm-wide components at one or both
83 a single sign requires defects and in the B7 splay is accommodated in the form of periodic splay stri
84 ying of the wHTH domains when Ile was bound; splaying is likely to account for the increased affinity
88 ymers increased the amount of induced saddle-splay membrane curvature and broadened the range of lipi
93 structure uniquely presented by the RPo: the splayed minor groove at the double-stranded/single-stran
96 otorious in this regard are the polarization splay modulated (B7) phases, in which the symmetry-requi
97 c field which originates in the periodically splay-modulated bulk of the LC rather than by surface st
98 extended to account for nonvanishing saddle splay modulus within lipid monolayers and perturbations
100 cusp (prolapse, restriction) and commissure (splaying) morphology; root pathology was less important.
101 r, 85% of the N-termini are splayed, and the splayed N-terminus can capture transport vesicles in vit
102 ranes: defensins selectively generate saddle-splay ("negative Gaussian") membrane curvature in model
103 es by generating topologically active saddle-splay ("negative Gaussian") membrane curvature through m
104 layed." However, it is impossible to achieve splay of a preferred sign everywhere in space unless app
106 ithin the optic tract region, meandering and splaying of axons in the optic tectum, and the induction
107 addition to drc-mutant axonemes resulted in splaying of doublets in the distal region, followed by o
109 ated to passing of the hydration barrier and splaying of lipids to eventually enter either the fully
110 In growth cones and at axon branch points, splaying of looped or bundled microtubules is accompanie
111 is proposed based on the structure, whereby splaying of the bottom of the pore is possible without r
112 type channels, the R165A mutation results in splaying of the cytoplasmic domains away from the centra
115 CodY-Ile derived from the tetramers showed a splaying of the wHTH domains when Ile was bound; splayin
120 ferating Cell Nuclear Antigen (PCNA) must be splayed open at one of the subunit-subunit interfaces by
123 extracellular-half of the pore-lining M2 is splayed open, reminiscent of the open conformation, whil
125 o DNA-binding domains of LacI are capable of splaying open about the tetramerization domain into an e
126 mpact bundle over hypothalamus, dramatically splay out over thalamus, and circumvent epithalamus as t
127 ch is equivalent to beta-strand 1 in LC8, is splayed out and binds to a crystallographic dimer as an
129 n the current structure, which is has an NTD splayed out with respect to previous structures, and oth
132 enylvinyl moiety in the TT isomer of 2Q gets splayed over the helical scaffold such that it is fraugh
133 ion as a replacement of energetically costly splay packing of the aggregates within the curved bipola
134 ive extrapolated-motion protocol to pack the splayed peripheral TM1 and TM2 transmembrane helices alo
138 polar smectic liquid crystals in which local splay prevails in the form of periodic supermolecular-sc
139 Depleted of nucleotide, NSF converts to a "splayed" protease-sensitive conformation that reveals it
140 that Tctp deficiency results in stunted and splayed retinotectal projections that fail to innervate
142 namic assembly and disassembly, bundling and splaying, severing, and rapid transport as well as integ
143 on of both Kid and NuMA in stark contrast to splayed spindle poles observed after perturbation of NuM
144 ons for the nine Usher-associated genes have splayed stereocilia, and some show delayed maturation of
145 play is accommodated in the form of periodic splay stripes spaced by defects and coupled to smectic l
146 t the SWI2/SNF2 chromatin-remodeling ATPases SPLAYED (SYD) and BRAHMA (BRM) are redundantly required
148 ly important target of the SNF2-class ATPase SPLAYED (SYD) in the shoot apical meristem of Arabidopsi
149 The SNF2-like chromatin-remodeling ATPase SPLAYED (SYD) was identified as a co-activator of floral
150 s thaliana SWI/SNF ATPases, BRAHMA (BRM) and SPLAYED (SYD), are viable, facilitating investigation of
153 g surface spanning the length of the DNA and splays the ends of the protospacer to allow each termina
156 their poles failed to converge, as MTs were splayed to discrete positions rendering deformed arrays.
159 helixes within each S100beta subunit form a splayed-type four-helix bundle (four perpendicular helix
162 bic fissure in bilayers for stalk formation, splay within the expanding hemifusion diaphragm, and fis
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