ライフサイエンスコーパス: alternative processing

1 bly uncover unknown compounds resulting from alternative processing.

2 ts role in regulating the gene expression by alternative processing.

3 indicate the existence of both redundant and alternative processing activities in seeds.

4 ation of developing macronuclei and promotes alternative processing by a Cbs-independent mechanism.

5 xample of exon skipping and the induction of alternative processing by cold stress to the small numbe

6 Given the ability of SR proteins to affect alternative processing decisions, our results suggest th

7 transposable element-induced disruptions in alternative processing demonstrate a role for the noncon

8 chains, which are regulated at the level of alternative processing during B cell differentiation.

9 ression, and also reveal examples of complex alternative processing, especially in brain, that may ha

10 ed host, while p48 was found to also undergo alternative processing independent of the encoded papain

11 over arise by a common mechanism, perhaps by alternative processing of a meiotic recombination initia

12 Alternative processing of APP in AD may increase product

13 Furthermore, alternative processing of BMP proproteins produces ligan

14 re, these results suggest that regulation of alternative processing of CT/CGRP could occur at the lev

15 ate their individual roles in regulating the alternative processing of doublesex, exuperantia and tra

16 These results suggest that alternative processing of erbAalpha mRNAs is regulated b

17 L-1beta processing should therefore consider alternative processing of IL-1beta in addition to caspas

18 FCA expression is regulated through alternative processing of its pre-mRNA.

19 Alternative processing of parvovirus B19 (B19V) pre-mRNA

20 Through alternative processing of pre-messenger RNAs, individual

21 In this study, the regulation of the alternative processing of pre-mRNA of both caspase 9 and

22 Alternative processing of pre-mRNA plays an important ro

23 Alternative processing of pre-mRNA transcripts is a majo

24 The alternative processing of prenylated CCaX motif proteins

25 ocess as well as a noncoding RNA produced by alternative processing of RNA transcribed from the same

26 processes including gene duplication and an alternative processing of scrambled genes.

27 nsory cortex and the hippocampus, suggesting alternative processing of social cues in these animals.

28 redundancy among DCL activities, leading to alternative processing of ta-siRNA precursors in the abs

29 inalis, which each have only one talin gene, alternative processing of talin mRNA also produces multi

30 slational control, alternative splicing, and alternative processing of the 3' end of mRNAs are all co

31 nown to regulate the non-neuronal pathway of alternative processing of the calcitonin/calcitonin gene

32 rge cohort of receptor subtypes arising from alternative processing of the GR gene.

33 These findings demonstrate that alternative processing of the human EGFR transcript prod

34 Alternative processing of the pre-messenger RNA encoding

35 ntron structure, patterns of expression, and alternative processing of their mRNAs.

36 To investigate the possibility of alternative processing of TNFalpha and/or IL-1beta by ne

37 Alternative processing of type II receptor transcripts t

38 We report here an alternative processing pathway of APP through the mammal

39 disruption of developmentally regulated RNA alternative processing pathways contributes to CDM disea

40 duction regulate the relative utilization of alternative processing pathways for the beta-amyloid pre

41 containing splice acceptor sites that create alternative processing pathways.

42 role in gene regulation can be modulated by alternative processing, resulting in shorter 3' UTRs.

43 00% additional cross peaks, when compared to alternative processing schemes.

44 omplex, containing multiple introns and many alternative processing sites, they are usually processed

45 d also freeze-drying proved to be a suitable alternative processing technique for most of the investi

46 ses a complex set of mRNAs generated through alternative processing that collectively encode three di

47 efensin variants with novel N termini due to alternative processing were identified in MMP7(-/-) cecu

48 Two forms resulting from alternative processing were identified.