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1  the nucleus where it is associated with the nuclear scaffold.
2 ry mechanism involving a multicomponent PIAS nuclear scaffold.
3  lithium 3,5-diiodosalicylate (LIS)-isolated nuclear scaffold.
4 ree cytoskeletal filament systems as well as nuclear scaffolds.
5 DNA elements postulated to interact with the nuclear scaffold and to mediate long-distance interactio
6 d in the nuclear membrane, disrupting proper nuclear scaffolding and causing the characteristic nucle
7 itiation and termination, and the eukaryotic nuclear scaffold attachments that partition chromosomes
8 tration of cellular proteins into an E4-ORF3 nuclear scaffold, but little is known about how this sma
9 the 30-nm fibers attached to a proteinaceous nuclear scaffold by an interaction between the scaffold
10         Surprisingly, cell-based analysis of nuclear scaffolds failed to confirm a MAR at this site,
11 ORF3 self-assembles into multimers to form a nuclear scaffold in infected cells and creates distinct
12 ith interphase chromosomes and copurify with nuclear scaffold, indicating that RNAs might impact inte
13  the genome as mediated by attachment to the nuclear scaffold/matrix and gene expression is not clear
14                           This suggests that nuclear scaffold/matrix association mediates a portion o
15                     DNA loop organization by nuclear scaffold/matrix attachment is a key regulator of
16  In parallel, analysis of association of the nuclear scaffold/matrix with the Ifng gene promoter has
17 tween integrins, cytoskeletal filaments, and nuclear scaffolds may therefore provide a discrete path
18 -Val-Ala-Asp fluoromethyl ketone) and of the nuclear scaffold multicatalytic proteinase (Ala-Pro-Phe
19            Our previous work showed that the nuclear scaffold (NS) protease is required for apoptosis
20 e permanently attached at their bases to the nuclear scaffold or matrix at sequences known as scaffol
21 rationally defined by their affinity for the nuclear scaffold or matrix.
22 ined no more of the motifs found attached to nuclear scaffolds or matrices (ie SARs or MARs) than wou
23 gions (BURs) are typically identified within nuclear scaffold- or matrix-attachment regions (S/MARs).
24 vely, 81% were associated with the AoAF cell nuclear scaffold (P < 0.001) and expressed.
25 osylphenylalanyl chloromethyl ketone and the nuclear scaffold protease inhibitor block lamin degradat
26 us nuclear BCL-2 regulates activation of the nuclear scaffold protease.
27 ogeria syndrome (HGPS), a mutant form of the nuclear scaffold protein lamin A distorts nuclei and seq
28  a subnuclear structure and may be part of a nuclear scaffold to which gene regulatory machinery bind

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