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1              We propose that the tight dsDNA spooling activates the switch that signals the headful c
2 creasing friction of a line around a central spool and quick release mechanisms used in electronics s
3                                         Such spools are only found when the tendency of nearby DNA st
4 ermini and ordered dsDNA coils in the capsid spooled around a disordered dsDNA core.
5                  In T7, the DNA is coaxially spooled around the cylindrical core protein, whereas the
6 PC-portal is incompatible with DNA coaxially spooled around the portal vertex, suggesting that newly
7 ese data establish that the T7 chromosome is spooled around this axis in approximately six coaxial sh
8 n of dsRNA segments each having a cone shape spooling around a transcription enzyme complex.
9  consist of 10-12 segments and exhibit a non-spooled arrangement mediated by RNA-dependent RNA polyme
10 in a folded conformation inconsistent with a spool conformation.
11  substrate or one where it is hauled off and spooled continuously to enable the production of continu
12  results suggest that gp1 functions as a DNA-spooling device, which may transform DNA into a specific
13 e infectious P22 virion reveals that tightly spooled DNA about the portal dodecamer forces a conforma
14   In proof-of-principle experiments based on spooled fibers, this was achieved by interleaving the qu
15  dsRNA viruses can adopt a dsDNA-like single-spooled genome organization.
16 onal machinery, predominantly display single-spooled genome organizations(1-8).
17  the DNA, we find that spatially ordered DNA spools have a much lower effective friction than disorde
18  a nucleosome as a wormlike chain bound to a spool, incorporating fluctuations in the number of bases
19 ctory mechanism in which unreplicated DNA is spooled into a centrally located replisome and newly syn
20 pared to single tape springs and that can be spooled into a compact state or unspooled to manipulate
21 es are engaged rapidly by ClpXP and are then spooled into the degradation chamber at a rate proportio
22 ypeptide to hydrolyse ATP to drive substrate spooling into ClpP, and would prevent stalling if one su
23                               This chromatin spool is further found to achieve large-scale helical tw
24 mation from feeding with rotation exhibits a spool-like character that is consistent with experimenta
25 arrangement of packaged DNA from toroidal to spool-like structures.
26                      This pattern suggests a spool model for DNA packaging, similar to that for some
27  in the deterministic fashion of the inverse-spool model, but rather is stochastic in character.
28 different than that suggested by the inverse spool model.
29 apsid packed in a manner consistent with the spool model.
30  first deposited and dried on a continuously spooling nickel wire.
31 tivity at 90 degrees C has yielded a diverse spool of selected sequences.
32 el binding sites of the FIR dimer results in spooling of a single strand of bound DNA, and suggests a
33 er of multiple copies into recipients by the spooling of copies generated on a master molecule by rol
34         Extensive strand exchange requires a spooling of duplex DNA into a recombinase-ssDNA complex,
35 than predicted by models that assume coaxial spooling of the DNA and interaction potentials derived f
36 dicted by models that assume coaxial inverse spooling of the DNA.
37 t of two nuclear spin memories through 40 km spools of low-loss fibre and a 35-km long fibre loop dep
38 ntral "structured" domain that comprises the spool onto which the DNA superhelix is wrapped and an N-
39 uctuations in the number of bases bound, the spool orientation, and the conformations of the unbound
40 components, which assemble into fibrils that spool out to elongate the Drosophila egg chamber.
41 s were elucidated based on electrochemistry, spooling photoluminescence, and ECL spectroscopy, unfold
42                                     When the spooling rig was used, a tape of the cellulose paper was
43                          Our newly developed spooling spectroscopy was employed during the ECL evolut
44 ities (AAA+) unfolding ring that unfolds and spools substrates into the peptidase chamber.
45 om a single ultra-powerful rotary motor that spools the DNA into a bacteriophage head, to hundreds of
46                Consequently, prophage DNA is spooled through the replication machinery, drawing the p
47 tems with lenses, polarizers, and mechanical spools, which are complex and cumbersome, and respond sl
48 pe-ratio mass spectrometer interfaced with a spooling wire microcombustion device.
49 ir delta(1)(3)C values were measured using a spooling-wire microcombustion device interfaced with an
50 ecules are wrapped into nucleosomes, protein spools with DNA.
51                       Our data reveal genome spooling within the capsid and identify putative recepto
52  axis and propose that this tilt assists DNA spooling without tangling during packaging.