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1 insights into function of U2AF and U2AF35 in alternative RNA processing.
2 G-quadruplexes, especially in the context of alternative RNA processing.
3 and 2) the presence of isoforms generated by alternative RNA processing.
4 r in the regulation of human calcitonin/CGRP alternative RNA processing.
5 ggests a novel role of U6 snRNP in regulated alternative RNA processing.
6 were likely expressed from a single gene by alternative RNA processing.
7 vels cannot be attributed to stage-regulated alternative RNA processing.
8 model systems for developmentally regulated alternative RNA processing.
9 t atypical splice site junctions to modulate alternative RNA processing.
10 The proposed method will fill a void among alternative RNA processing analysis tools for transcript
13 nome methylation patterns, and regulation of alternative RNA processing by intronic heterochromatin.
15 indicating that promoter identity influences alternative RNA-processing decisions have created intere
18 ion of both isoforms preferentially modified alternative RNA processing events without widespread fai
19 modifications, transcription elongation, and alternative RNA processing in IgH mRNA production, we pe
20 results are the first to establish a role of alternative RNA processing in specifying the post-endocy
21 alternative splicing indicate that extensive alternative RNA processing is associated with many prote
23 well conserved and that, like melanogaster, alternative RNA processing is responsible for its sex-sp
25 lated peptide-alpha (CGRPalpha), produced by alternative RNA processing of the CT/CGRP gene, has no c
28 cations for the origin of genes that contain alternative RNA processing reactions at their 5' or 3' e
29 n mu gene plays a central role in regulating alternative RNA processing to produce RNAs that encode m
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