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1 erases, or a lower-than-equilibrium level of catenation).
2 on activity and catalyze single-stranded DNA catenation.
3 o much higher H(2) uptake in the isomer with catenation.
4 n two plasmids, either unlinked or linked by catenation.
5 leads to high levels of knotting and reduced catenation.
6 r mitosis since it resolves sister chromatid catenations.
7                    Crucially, persistence of catenation after S phase depends on cohesin.
8 , and replication protein A (RPA) coordinate catenation and decatenation of dsDNA through sequential
9  been summarized into three main categories, catenation and interpenetration, chemical bonding enhanc
10 hen mitotic cells are challenged by retained catenation and this delayed exit is characterized by Bub
11 s to switch from DNA unlinking to active DNA catenation, and depends on an unstructured C-terminal re
12 ster chromatids--commonly referred to as DNA catenation--and as sister chromatid linkages generated b
13 stem has been used to explore whether excess catenation arising through topo 2 depletion is sufficien
14 ircular minichromosomes are held together by catenation as well as by cohesin.
15 es just as well when held near the target by catenation as when co-linear with the target.
16 lysis shows high diastereoselectivity during catenation, as only a single (Z)-isomer is formed.
17  stronger Ge-N interactions and quenching of catenation behaviour: reduction of Ar(NEt2) GeCl gives t
18 y directly staining DNA, we observe that DNA catenation between sister chromatids (separated by fluid
19 merase II (topo II), the enzyme that removes catenation between sister chromatids left behind after c
20 egation requires the removal of cohesion and catenation between sister chromosomes, two physical link
21 e II completely removes DNA intertwining, or catenation, between sister chromatids before they are se
22 e chromosome supercoiling, condensation, and catenation by moving one double-stranded DNA segment thr
23 ures up to 50 bar demonstrate that framework catenation can be favorable for the enhancement of hydro
24 ications for understanding the nature of the catenation checkpoint, how DNA replication terminates, h
25 mulation of DNA damage, RF rotation, and pre-catenation, confirming that cohesin-dependent DNA topolo
26 hrough a counterintuitive modulator-directed catenation control approach.
27 d DNA passage activity that can mediate both catenation-decatenation processes and changes in DNA top
28 in the control of DNA supercoiling or in DNA catenation/decatenation during recombination and chromos
29 ation, whereas Topo III is more efficient at catenation/decatenation, probably reflecting their diffe
30                        The efficiency of the catenation depends on the distance between opposing segm
31                  We suggest that labile gp45 catenation directly generates the coupling of late trans
32  mechanism for regulation of centromeric DNA catenation during mitosis by PIASy-mediated SUMOylation
33 lignant CD4(+)CD8(+) T cells show persistent catenations during chromosome segregation, triggering DN
34 o reveal linear additivity in beta(vec) with catenation for all benzoic acid-containing chromophores
35                        (3) Increased arylene catenation from two to three to four rings (2TTMC--> 3TT
36 n MOF synthesis is the strong propensity for catenation (growth of multiple independent networks with
37                                          DNA catenation has been implicated in both sister chromatid
38                            Interpenetration (catenation) has long been considered a major impediment
39 f the following: (i) oligothiophene backbone catenation; (ii) naphthalenediimide vs perylenediimide c
40  depends on multiple hydrogen bonds to guide catenation in a point-contact manner, resulting in high
41 cule to the open TRR-ssDNA gate, followed by catenation in each case.
42 mosome integrity in cells failing to resolve catenation in G2.
43  we determine that the metaphase response to catenation in mammalian cells operates through PKCepsilo
44                              When delayed by catenation in mitosis, inhibition of PKCepsilon results
45 ification of the chiroptical properties upon catenation, indicating stabilization of the helical seco
46 opsch for carbon monoxide (CO) hydrogenative catenation involves C-C coupling from a carbide-derived
47                                    Chromatid catenation is actively monitored in human cells, with pr
48  are correctly bioriented, and that residual catenation is resolved, permitting complete sister chrom
49                      One strategy to achieve catenation is the design of pre-annular molecules that a
50 cal outcomes - for example, decatenation vs. catenation - is poorly understood.
51        Mechanical interlocking of molecules (catenation) is a nontrivial challenge in modern syntheti
52 rption studies have been carried out for the catenation isomer pairs of PCN-6 and PCN-6' (both have t
53              These MOFs exhibited remarkable catenation isomerism that is controlled by both chiralit
54 pation of hypernegative DNA supercoiling and catenation/knotting.
55 int attenuation occur even in the absence of catenation linking sister chromatids.
56  also function in vivo in removing the final catenation links remaining upon completion of DNA replic
57 verall chromosome shape, suggesting that DNA catenation must be simultaneously maintained for correct
58 ber of supercoils that are converted to four catenation nodes by Xer strand exchange.
59  closure and secondary nucleation, a maximum catenation number of 22 was confirmed by atomic force mi
60  as plausible intermediates in the reductive catenation of C(1) oxygenates.
61  previously been shown to catalyze reductive catenation of carbon monoxide (CO) to ethylene, ethane,
62 merase II, cohesin stimulates intermolecular catenation of circular DNA molecules.
63  X-ray diffraction reveals how the five-fold catenation of diamonoid systems, stabilized by hydrogen
64 by crosslinking its three interfaces induces catenation of individual and sister DNAs.
65 efficiently induce topoisomerase II mediated catenation of plasmid DNA in vitro and is the only membe
66 vely and positively supercoiled plasmid DNA, catenation of plasmid DNA, and decatenation of kinetopla
67  that is associated with non-disjunction and catenation of sister chromatids.
68                               Disrupting the catenation of the chromosomes with Topoisomerase IIalpha
69 ng single-stranded DNA circles that leads to catenation of the circles.
70 tion to the pi-donor ring and the subsequent catenation of the pi-donor ring by the pi-acceptor ring
71 ng the very large NLO response: (1) For ring catenation of three or greater, sterically enforced pi-s
72 s DNA we discovered that it can also mediate catenation of two DNA rings, an intermolecular reaction.
73 y employing suitable diisonitriles, even the catenation of two open-shell singlet cyclopentane-1,3-di
74                                              Catenations of DNA formed during replication are decaten
75  2 depletion is sufficient to trigger the G2 catenation (or decatenation) checkpoint, proposed to exi
76 esults lend support to certain models of DNA catenation organization and regulation: in particular, w
77                           This suggests that catenation prevents sister-rDNA segregation but that yea
78                    We observe this transient catenation process indirectly using ensemble methods, su
79 pendent networks within a given crystal), as catenation reduces cavity sizes and diminishes porosity.
80 ha phosphorylation, a response necessary for catenation resolution during mitosis.
81 ation initiation indeed causes increased DNA catenation, resulting in DNA damage and chromosome loss.
82  of checkpoint activation in response to the catenation state of DNA.
83                          Here, we follow the catenation status of circular minichromosomes of three s
84 suggested that this unusually high degree of catenation stems from the secondary nucleation of the pr
85                  Here we report a controlled catenation strategy in hydrogen-bonded organic framework
86 is coupled to a reduction in DNA complexity (catenation, supercoiling, and knotting) below the level
87 m our observation of centromere-concentrated catenation that spindle forces could play a driving role
88 ring prometaphase, where it resolves the DNA catenations that represent the last link between sister
89                                To facilitate catenation, the circles were brought into close proximit
90 se of the difficulty of observing chromosome catenation, this link has remained indirect.
91 d boron share the important property of self-catenation thus these elements can produce individually
92                      The contribution of DNA catenation to sister chromatid cohesion is unclear partl
93  responses, which can be controlled by their catenation topologies.
94                                     Nitrogen catenation under high pressure leads to the formation of
95           The ability of MukB to mediate DNA catenation underscores its potential for bringing distal
96 phase chromosomes display residual levels of catenations, upon timely removal of condensin I, chromos
97 tion, B-H borane bond activation, and borane catenation via metal-mediated dehydrocoupling to form el
98 nimal DNA duplex length at which we detected catenation was 50-60 bp for DNA gyrase and 40 bp for top
99                                 For Topo IV, catenation was observed when one, but not both, of the D
100 oscale toroids revealed a high percentage of catenation, which is sufficient to yield 'nanolympiadane