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1 egion (3'-UTR) and inhibiting translation or RNA stability.
2 an, in part, be attributed to alterations in RNA stability.
3 in during the cell cycle correlate with SsrA RNA stability.
4 id not detectably affect mRNA translation or RNA stability.
5 *971T) accounts for the observed increase in RNA stability.
6 ted regulation of cyclooxygenase-2 messenger RNA stability.
7 ects on the transcription initiation rate or RNA stability.
8 ot just protein synthesis but also messenger RNA stability.
9 t be included in the predictions of tertiary RNA stability.
10 tion in the 3'untranslated region may affect RNA stability.
11 cause it could be accounted for by increased RNA stability.
12 nd deletion-mutant mRNAs were independent of RNA stability.
13 ne transcription but also affects coreceptor RNA stability.
14 e novo protein synthesis and does not affect RNA stability.
15 criptional mechanisms involving differential RNA stability.
16 tion occurs at the level of transcription or RNA stability.
17 binding enhanced pestivirus translation and RNA stability.
18 s seen in nuclear RNA and was independent of RNA stability.
19 fore plays a significant role in determining RNA stability.
20 ting an effect at the transcription level or RNA stability.
21 ell surface HSA expression by modulating its RNA stability.
22 without antisense transcription to regulate RNA stability.
23 It did not appear to affect RNA stability.
24 mRNA should not be hampered by problems with RNA stability.
25 ription, indicating that SM enhances nuclear RNA stability.
26 l GAAA tetraloop, a motif known for enhanced RNA stability.
27 s partially controlled by gene expression or RNA stability.
28 reased gene transcription, with no effect on RNA stability.
29 ing splicing, transport, polyadenylation and RNA stability.
30 of conditions that might have affected HIV-1 RNA stability.
31 but selection of these sites does not affect RNA stability.
32 echanisms, one of which is the modulation of RNA stability.
33 ALAT1 at the level of both transcription and RNA stability.
34 ther events in the RNA life cycle, including RNA stability.
35 t of CsrA on translation, RNA abundance, and RNA stability.
36 require SM for efficient expression, such as RNA stability.
37 eliminates the miR-122 requirement for viral RNA stability.
38 ication rates of HCV RNA, but affected viral RNA stability.
39 reduced lipid accumulation by reducing PLIN2 RNA stability.
40 affects each step of protein expression and RNA stability.
41 through translational efficiency rather than RNA stability.
42 ding sequences were associated with enhanced RNA stability.
43 of transcription, translation, splicing, and RNA stability.
44 aling of sRNAs to target mRNAs and to affect RNA stability.
45 NA, suggesting that REF/Aly promotes nuclear RNA stability.
46 rtance of RNA maturation as a determinant of RNA stability.
47 s, which are not accounted for by changes in RNA stability.
48 ate transcription, splicing, translation, or RNA stability.
49 plays a critical role in mRNA expression and RNA stability.
50 l ancillary factors that control editing and RNA stability.
51 identified with a function in mitochondrial RNA stability.
52 senger RNAs by export-independent effects on RNA stability.
53 its low rate of transcription and messenger RNA stability.
54 e expression at the level of translation and RNA stability.
55 ligand binding sites and metal ion-dependent RNA stabilities.
61 slation of the TRR is necessary for extended RNA stability and for expression of the transcriptional
62 emically modified nucleotides, which enhance RNA stability and increase affinity in Watson-Crick base
63 n of CAR gene transcription, whereas altered RNA stability and increased proteasomal protein degradat
65 es, the role of 2' O-methyl modifications in RNA stability and innate immune sensing, and functions o
66 tion, how FXR1 regulates its targets through RNA stability and luciferase assays, and functional cons
73 modifications exhibit a range of effects on RNA stability and structure, depending on their location
75 We found that Cas9 is essential for guide RNA stability and that the nuclear Cas9-guide RNA comple
76 shes between mRNAs regulated at the level of RNA stability and those regulated at the level of transl
78 mRNAs and has been implicated in control of RNA stability and translation and selective cap-independ
79 family of RNA binding proteins that regulate RNA stability and translation by binding to specific seq
80 ility that this 5' NAD(+) cap could modulate RNA stability and translation on specific subclasses of
81 rocessing and ribosome assembly and includes RNA stability and translation regulation within mitochon
82 , RNA processing and modification, messenger RNA stability and translation, and even protein degradat
83 ibitory effect of rapamycin was on messenger RNA stability and translation, rather than on IL-2 trans
90 matin modification, transcription, messenger RNA stability and ubiquitination, and another implicated
91 l of incompletely spliced RNAs by increasing RNA stability and was associated with a twofold down-reg
93 itic spine morphology, protein and messenger RNA stability, and catalytic activity were examined.
94 tes efficient nuclear-cytoplasmic transport, RNA stability, and cytoplasmic utilization of unspliced
95 ulating transcription, alternative splicing, RNA stability, and intracellular localization of the vir
97 ative mRNA splicing, SR protein trafficking, RNA stability, and possibly the generation of autoantibo
103 in level was not a consequence of changes in RNA stability, as indicated by Northern blot analysis.
104 ke 2 (ELAVL2), a brain-specific regulator of RNA stability, as presumptive targets of three of four e
109 otein-RNA binding with concurrent changes in RNA stability at specific time points following activati
112 ing proteins, Puf, regulates translation and RNA stability by binding to specific sequences in the 3'
113 mal to the 3' end indicates that it mediates RNA stability by blocking the assembly, but not the acti
115 tory mechanism whereby ADAR2 enhances target RNA stability by limiting the interaction of RNA-destabi
117 ion and a novel mutation that increases mtrC RNA stability conferred the highest levels of derepressi
118 on that the La protein may contribute to HBV RNA stability, constitutively and in response to inflamm
120 lification, with an additional effect on HCV RNA stability/degradation detectable at a dose of 250 U/
125 ylated 5'-guanosine cap that is required for RNA stability, efficient translation, and protection fro
126 es of the rnc transcript comprise a portable RNA stability element (rncO) that contains all of the ci
127 ulates in cells by using a 3'-triple-helical RNA stability element for nuclear expression (ENE).
128 ry RNA elements, termed sRSEs for structural RNA stability elements, which are significantly overrepr
132 , signal transducers, transcription factors, RNA stability factors, and epigenetic modulators that ac
133 cluding inherent RNA shields, hijacking host RNA stability factors, incapacitating the host decay mac
135 les of the P-4 nuclease in the amastigote in RNA stability (gene expression) or DNA repair are discus
138 d to play roles in transcription and nuclear RNA stability in addition to its more broadly characteri
139 chinery and changing the entire landscape of RNA stability in cells using virally encoded nucleases.
141 e furthermore found increased matK messenger RNA stability in mature tissue, while other chloroplast
147 be partly achieved at the level of messenger RNA stability, in which the targeted destruction of subs
148 tic replication but may contribute to target RNA stability independent of effects on RNA export, sugg
149 the nascent transcript and PHLDA1 messenger RNA stability, indicating both transcriptional and post-
151 mental and simulation results establish that RNA stability is largely determined by a combination of
152 ontrast, the contribution of site-binding to RNA stability is often quite small because of the large
153 LCK expression in cancer cells by decreasing RNA stability, leading to increased cell proliferation.
159 NAs, little is known about the influences of RNA stability, mRNA quality control and compartmentaliza
160 f mRNA metabolism, including nuclear export, RNA stability, mRNA quality control, and translation.
161 pression processes, including transcription, RNA stability, mRNA transport, and translational control
162 s from transcription (SP5, YAP1, and RUNX1), RNA stability (MSI2), and protein stability (CUL4A).
163 es had similarity to proteins that influence RNA stability, namely a ribonuclease activator, the pumi
164 d alphaCP-2, implicated in the regulation of RNA stability of alpha-globin and tyrosine hydroxylase m
166 chromatin organization, gene transcription, RNA stability or RNA translation is not well understood,
167 ERI3 is not required for maintaining DENV-2 RNA stability or translation of the viral polyprotein, b
169 eterious, impairing transcription, splicing, RNA stability, or protein function, as well as imposing
173 quence-specific guides to regulate messenger RNA stability, protein synthesis, chromatin organization
174 st widespread interindividual differences in RNA stability related to DNA sequence and composition va
175 T cells from healthy donors increases HIV-1 RNA stability, rendering the cells permissive for HIV-1
176 ssing, although the relationship between Alu RNA stability, scAlu RNA production, and retroposition h
178 According to this approach, low ribosomal RNA stability should decrease the precision of protein s
182 functional RNA domains within roX1, assaying RNA stability, targeting of the MSL proteins to the X, a
183 ortant link between DNA damage signaling and RNA stability that may be relevant to cell cycle regulat
184 f eukaryotic mRNAs regulates translation and RNA stability through an association with the poly(A)-bi
185 measurements are used with other measures of RNA stability to develop an overall picture of the energ
186 a that localize key sequence determinants of RNA stability to the 3' end of RNA7.2 and suggest that s
187 y significant association between non-coding RNA stability, transcript length and predicted secondary
189 nance of mitochondrial genome, mitochondrial RNA stability, translation, and respiratory function.
195 of the changes in mRNA abundance were due to RNA stability, we found a smaller but more interesting p
198 oter, and their effects on transcription and RNA stability were evaluated both in vitro and in vivo.
199 up-regulated by both increased synthesis and RNA stability while down-regulated genes were suppressed
201 e for opposing effects of polyadenylation on RNA stability within a single organelle and suggests a n
202 ted regions regulate mRNA trans-splicing and RNA stability, yet where UTRs begin and end is known for
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