ライフサイエンスコーパス: interchromatin

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1 the gene, NXF1 binds to BR mRNPs only in the interchromatin.

2 nger RNA protein complexes (mRNPs) enter the interchromatin.

3 teady state, a subset of the BR mRNPs in the interchromatin binds NXF1, UPF2, and UPF3.

4 restricts viral capsid diffusion, but due to interchromatin channels capsids are able to reach the nu

5 ovement of large macromolecular complexes to interchromatin corrals.

6 rent herpesviruses induced an enlargement of interchromatin domains and allowed particles to diffuse

7 pre-mRNA splicing machinery are localized in interchromatin granule clusters (IGCs) and perichromatin

8 To examine the involvement of interchromatin granule clusters (IGCs) in transcription

9 n on nuclear structures known as speckles or interchromatin granule clusters (IGCs) revealed by immun

10 SK RNA to be enriched in nuclear speckles or interchromatin granule clusters (IGCs), a subnuclear dom

11 lized to the nucleus and was concentrated in interchromatin granule clusters (IGCs), sites where spli

12 bition results in accumulation of DEK within interchromatin granule clusters (IGCs), sub-nuclear stru

13 stribution that predominantly corresponds to interchromatin granule clusters (IGCs).

14 roviral cyclin (RV-cyclin) that localizes to interchromatin granule clusters and binds CDK8.

15 Furthermore, Dfa(A) was present in the interchromatin granule clusters and was also found to bi

16 d, most of which are accumulated in enlarged interchromatin granule clusters in the nucleoplasm of RC

17 ctural level, perispeckles are distinct from interchromatin granule clusters that may function as sto

18 Nuclear speckles, or interchromatin granule clusters, are enriched in factors

19 d concentration of the IL-1alpha propiece in interchromatin granule clusters, concentrations of prote

20 s revealed that these speckles correspond to interchromatin granule clusters.

21 splicing factors and poly(A)+ RNA were fused interchromatin granule clusters.

22 sembles, but is functionally different from, interchromatin granule clusters.

23 wn structures such as the coiled body or the interchromatin granule.

24 rol genes between Polycomb bodies (PcGs) and interchromatin granules (ICGs) in response to growth sig

25 teractions responsible for the clustering of interchromatin granules are disrupted when SR proteins a

26 30-nm particles, which closely resemble the interchromatin granules described from sections of somat

27 lap with structures previously identified as interchromatin granules or spliceosomal speckles.

28 lizes to punctate structures consistent with interchromatin granules that show a striking adjacent-lo

29 nterchromosomal interaction loci to distinct interchromatin granules, long thought to be "storage" si

30 ch we have shown previously to coincide with interchromatin granules.

31 r, nascent RNA synthesis was observed in the interchromatin regions of the cells studied and spatiall

32 The interchromatin space is composed of nuclear subcompartme

33 Poly(A) RNA can move freely throughout the interchromatin space of the nucleus with properties char

34 Our ability to measure large strains in the interchromatin space, which reveals that movement of chr

35 aments coursing dendritically throughout the interchromatin space?

36 mplexes is restricted to the extranucleolar, interchromatin spaces.

37 ions, and their transcripts frequently share interchromatin trafficking channels.

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