ライフサイエンスコーパス: nuclear scaffold

1 lithium 3,5-diiodosalicylate (LIS)-isolated nuclear scaffold.

2 the nucleus where it is associated with the nuclear scaffold.

3 ry mechanism involving a multicomponent PIAS nuclear scaffold.

4 ree cytoskeletal filament systems as well as nuclear scaffolds.

5 emerged in recent years as chromatin-binding nuclear scaffolds, able to influence target gene express

6 DNA elements postulated to interact with the nuclear scaffold and to mediate long-distance interactio

7 d in the nuclear membrane, disrupting proper nuclear scaffolding and causing the characteristic nucle

8 genome is anchored and regulated by various nuclear scaffolds and structures, including the nuclear

9 itiation and termination, and the eukaryotic nuclear scaffold attachments that partition chromosomes

10 tration of cellular proteins into an E4-ORF3 nuclear scaffold, but little is known about how this sma

11 the 30-nm fibers attached to a proteinaceous nuclear scaffold by an interaction between the scaffold

12 the significance of chromatin regulators and nuclear scaffold dynamics in promoting light-induced pla

13 Surprisingly, cell-based analysis of nuclear scaffolds failed to confirm a MAR at this site,

14 Lamin A/C provides a nuclear scaffold for compartmentalization of genome func

15 ucleus of cancer cells, where it has a novel nuclear scaffolding function that controls gene expressi

16 ORF3 self-assembles into multimers to form a nuclear scaffold in infected cells and creates distinct

17 ith interphase chromosomes and copurify with nuclear scaffold, indicating that RNAs might impact inte

18 NA-seq analysis reveals that most RNA in the nuclear scaffold is repeat-rich, non-coding, and derived

19 the genome as mediated by attachment to the nuclear scaffold/matrix and gene expression is not clear

20 This suggests that nuclear scaffold/matrix association mediates a portion o

21 DNA loop organization by nuclear scaffold/matrix attachment is a key regulator of

22 ithin enhancer elements, as well as within a nuclear scaffold/matrix attachment region.

23 In parallel, analysis of association of the nuclear scaffold/matrix with the Ifng gene promoter has

24 tween integrins, cytoskeletal filaments, and nuclear scaffolds may therefore provide a discrete path

25 -Val-Ala-Asp fluoromethyl ketone) and of the nuclear scaffold multicatalytic proteinase (Ala-Pro-Phe

26 Our previous work showed that the nuclear scaffold (NS) protease is required for apoptosis

27 e permanently attached at their bases to the nuclear scaffold or matrix at sequences known as scaffol

28 rationally defined by their affinity for the nuclear scaffold or matrix.

29 ined no more of the motifs found attached to nuclear scaffolds or matrices (ie SARs or MARs) than wou

30 gions (BURs) are typically identified within nuclear scaffold- or matrix-attachment regions (S/MARs).

31 vely, 81% were associated with the AoAF cell nuclear scaffold (P < 0.001) and expressed.

32 osylphenylalanyl chloromethyl ketone and the nuclear scaffold protease inhibitor block lamin degradat

33 us nuclear BCL-2 regulates activation of the nuclear scaffold protease.

34 ogeria syndrome (HGPS), a mutant form of the nuclear scaffold protein lamin A distorts nuclei and seq

35 relamin A, the farnesylated precursor of the nuclear scaffold protein lamin A.

36 Here we demonstrate that loss of the nuclear scaffolding protein Matrin-3 (Matr3) in erythroi

37 proliferating cell nuclear antigen (PCNA), a nuclear scaffolding protein pivotal in DNA synthesis, co

38 WD repeat domain 5 (WDR5) is a nuclear scaffolding protein that forms many biologically

39 a subnuclear structure and may be part of a nuclear scaffold to which gene regulatory machinery bind