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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 RNAs are heterogeneous with respect to their alternative processing and secondary structures, but the
5 ation of developing macronuclei and promotes alternative processing by a Cbs-independent mechanism.
6 xample of exon skipping and the induction of alternative processing by cold stress to the small numbe
7   Given the ability of SR proteins to affect alternative processing decisions, our results suggest th
8  transposable element-induced disruptions in alternative processing demonstrate a role for the noncon
9  chains, which are regulated at the level of alternative processing during B cell differentiation.
10 ression, and also reveal examples of complex alternative processing, especially in brain, that may ha
11 ed host, while p48 was found to also undergo alternative processing independent of the encoded papain
12                This information will sustain alternative processing leading to SCC products with tail
13 ridin levels, suggesting its potential as an alternative processing method.
14 -mechanics and glass physics and may suggest alternative processing methods to epitaxially grow metal
15 alysis methodologies must be used to compare alternative processing methods.
16 over arise by a common mechanism, perhaps by alternative processing of a meiotic recombination initia
17                                              Alternative processing of APP in AD may increase product
18                                 Furthermore, alternative processing of BMP proproteins produces ligan
19 re, these results suggest that regulation of alternative processing of CT/CGRP could occur at the lev
20 ate their individual roles in regulating the alternative processing of doublesex, exuperantia and tra
21                   These results suggest that alternative processing of erbAalpha mRNAs is regulated b
22 L-1beta processing should therefore consider alternative processing of IL-1beta in addition to caspas
23          FCA expression is regulated through alternative processing of its pre-mRNA.
24                                              Alternative processing of mRNA, a phenomenon that has be
25                                              Alternative processing of parvovirus B19 (B19V) pre-mRNA
26                                              Alternative processing of perturbed forks has been assoc
27                                      Through alternative processing of pre-messenger RNAs, individual
28         In this study, the regulation of the alternative processing of pre-mRNA of both caspase 9 and
29                                              Alternative processing of pre-mRNA plays an important ro
30                                              Alternative processing of pre-mRNA transcripts is a majo
31                                          The alternative processing of prenylated CCaX motif proteins
32 ocess as well as a noncoding RNA produced by alternative processing of RNA transcribed from the same
33 ption of eukaryotic genomes involves complex alternative processing of RNAs.
34  processes including gene duplication and an alternative processing of scrambled genes.
35 nsory cortex and the hippocampus, suggesting alternative processing of social cues in these animals.
36  redundancy among DCL activities, leading to alternative processing of ta-siRNA precursors in the abs
37 inalis, which each have only one talin gene, alternative processing of talin mRNA also produces multi
38 slational control, alternative splicing, and alternative processing of the 3' end of mRNAs are all co
39  C (FLC) is cotranscriptionally repressed by alternative processing of the antisense transcript COOLA
40 nown to regulate the non-neuronal pathway of alternative processing of the calcitonin/calcitonin gene
41 rge cohort of receptor subtypes arising from alternative processing of the GR gene.
42              These findings demonstrate that alternative processing of the human EGFR transcript prod
43                                              Alternative processing of the pre-messenger RNA encoding
44 ntron structure, patterns of expression, and alternative processing of their mRNAs.
45            To investigate the possibility of alternative processing of TNFalpha and/or IL-1beta by ne
46                                              Alternative processing of type II receptor transcripts t
47 f intergenic RNAs that distinguishes between alternative processing of well-annotated genes from inde
48                            We report here an alternative processing pathway of APP through the mammal
49  disruption of developmentally regulated RNA alternative processing pathways contributes to CDM disea
50 duction regulate the relative utilization of alternative processing pathways for the beta-amyloid pre
51                                  The role of alternative processing pathways may help coordination of
52 containing splice acceptor sites that create alternative processing pathways.
53  role in gene regulation can be modulated by alternative processing, resulting in shorter 3' UTRs.
54 00% additional cross peaks, when compared to alternative processing schemes.
55 omplex, containing multiple introns and many alternative processing sites, they are usually processed
56 d also freeze-drying proved to be a suitable alternative processing technique for most of the investi
57 ses a complex set of mRNAs generated through alternative processing that collectively encode three di
58 efensin variants with novel N termini due to alternative processing were identified in MMP7(-/-) cecu
59                     Two forms resulting from alternative processing were identified.