戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 ion, due to augmented gene transcription and mRNA instability.
2 , frequent de novo mutations, and associated mRNA instability.
3  of their mRNAs that confer a high degree of mRNA instability.
4  and others did not significantly affect tau mRNA instability.
5 leads to nucleolin down-regulation and bcl-2 mRNA instability.
6 lysomes and appeared to correlate with CD154 mRNA instability.
7 coding region which appear to be involved in mRNA instability.
8  that this response was not due to increased mRNA instability.
9 ocation of amino acid residues in conferring mRNA instability.
10 r create frameshifts both of which result in mRNA instability.
11                      The mutation results in mRNA instability and a premature termination codon in th
12 ation in RDEB: one involving PTCs leading to mRNA instability and absence of protein synthesis, the o
13 11 in targeting nucleolin and inducing bcl-2 mRNA instability and cytotoxicity in these cells.
14 still exhibit critical limitations caused by mRNA instability and degradation, which are major obstac
15   However, their optimization is hindered by mRNA instability and inefficient protein expression.
16 gag INS element, known to be inactive in gag mRNA instability assays, was unable to complement the Re
17 ation in transgenic mice by mutating a major mRNA instability determinant in a light neurofilament (N
18 tor in cells that could override the nuclear mRNA instability determinant.
19 ast, the 3' UTR was found to act as a potent mRNA instability determinant.
20 seases-causing TDP-43 mutations affected tau mRNA instability differentially, in that some promoted a
21 lus is an essential site of inflammatory pre-mRNA instability during infection.
22                           Binding of a bcl-2 mRNA instability element (AU-rich element-1) to nucleoli
23 he soybean DST element was more active as an mRNA instability element than the mutant version and the
24 A and bla have been used to identify a novel mRNA instability element.
25 rent construct, suggesting that CAT-specific mRNA instability elements may serve as dominant negative
26 ed the interaction between HuD and prototype mRNA instability elements of the sequence UU(AUUU)(n)AUU
27 e molecular basis of TNF-alpha-mediated eNOS mRNA instability, eNOS 3' untranslated region (3'-UTR) b
28 inding in a cell-free system and TTP-induced mRNA instability in cell transfection experiments.
29 NA splicing to eliminate signals that confer mRNA instability in nonproliferating cells.
30 at some A/U-rich sequences can contribute to mRNA instability in plants.
31                                        IFRD1 mRNA instability in resting cells requires translation o
32 on demonstrated that the determinant of petD mRNA instability in the mcd1-1 background is located in
33 ing its CNBD can still act to promote target mRNA instability in vitro and in vivo These data have im
34 rosis factor alpha (TNFalpha) messenger RNA (mRNA) instability in murine macrophages.
35                  Results show that cyclin D3 mRNA instability induced by L-Arg deprivation is depende
36 idopsis (Arabidopsis thaliana) revealed that mRNA instability is associated with a group of genes con
37  expression data for these genes argues that mRNA instability is of high significance during plant re
38 crease plant performance and, theoretically, mRNA instability may facilitate faster recovery.
39 the presence of multiple copies of the AUUUA mRNA instability motif in its 3'-untranslated end.
40                                    No A(U)nA mRNA instability motifs were present.
41                     These include a putative mRNA instability mutation in dwf5-1, 3' and 5' splice-si
42                  Finally, dark-induced Fed-1 mRNA instability occurs even when most of the mRNA is re
43 aracterized by transcription suppression and mRNA instability of eNOS complemented by upregulation of
44            The cis-element required for SOS1 mRNA instability resides in the 500-bp region within the
45 ects); in two of them, COL1A2 messenger RNA (mRNA) instability results from compound heterozygosity f
46 he abundance of mRNAs that contain the plant mRNA instability sequence called DST (downstream element
47                                  A number of mRNA instability sequences that mediate rapid mRNA decay
48  same regions also mediated TDP-43-dependent mRNA instability, suggesting a mechanism by which TDP-43
49 3 suppressed tau expression by promoting its mRNA instability through the UG repeats of its 3-untrans
50  are also enriched in motifs associated with mRNA instability, transcriptional inhibition experiments
51 es from wild-type and TTP-deficient mice, KC mRNA instability was found to be highly dependent on TTP
52 ated overexpression of eEF1A1 increased eNOS mRNA instability, whereas knockdown of eEF1A1 substantia