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1 igh p-eIF2 levels that would otherwise cause translational arrest.
2  the HSV-1 protein gamma34.5 for reversal of translational arrest.
3 o stress-granules (SGs), known sites of mRNA translational arrest.
4 t ribosome pauses, but responds to prolonged translational arrest.
5 sting that increased recoding alleviates the translational arrest.
6 RNA production and promotes arsenite-induced translational arrest.
7 hibits arsenite-induced tiRNA production and translational arrest.
8 iRNAs promotes phospho-eIF2alpha-independent translational arrest.
9 ion by means of targeted RNA degradation and translational arrest.
10 -functional ribosomal components and undergo translational arrest.
11 reonine kinases that regulate stress-induced translational arrest.
12 isense ORNs is mediated through a process of translational arrest.
13 nt deprivation through a mechanism involving translational arrest.
14 L where stop-gain variants trigger a similar translational arrest.
15 s of helix formation and how VemP causes the translational arrest.
16  therefore unrestricted by their concomitant translational arrest.
17 slation elongation (No-Go), which results in translational arrest.
18  control mechanism that evolved to cope with translational arrests.
19 red rapidly (<15 min) and resulted in modest translational arrest, a fundamental homeostatic response
20 damage response in vertebrates, which causes translational arrest and apoptosis.
21                                Inhibition of translational arrest and ER stress by salubrinal or of M
22 terplay with the Arg-Leu-Arg motif to induce translational arrest and illuminate the basis for the le
23 tain amino acid sequences induce very strong translational arrest and provide a toolbox of APs of var
24  of PKR, an eIF2alpha kinase, which triggers translational arrest and the formation of stress granule
25                               This regulated translational arrest and yidC2 induction require a speci
26 type-dependent induction of stress granules, translational arrest, and growth impairment in a manner
27 d otherwise stimulate the cell's autophagic, translational-arrest, and type I interferon responses to
28 iosynthetic processes and that apoptosis and translational arrest are linked.
29 lly target messenger RNAs for degradation or translational arrest are the best-understood class of sR
30               Nonfunctional 18S rRNA induces translational arrest at start sites.
31  a local storage compartment for mRNAs under translational arrest but are poised for release to activ
32 ecific ribosomal proteins, and conditions of translational arrest, but their relative contribution to
33 regulates autophagy, it is the prevention of translational arrest by ICP34.5 rather than its control
34 f certain polypeptides that initially bypass translational arrest can be stopped at later stages of e
35                         In Escherichia coli, translational arrest can elicit cleavage of codons withi
36 c communication within the ribosomal tunnel, translational arrest, chaperone interaction, folding, an
37 e receptor activation failed to liberate the translational arrest conferred by the 3'-UTR of TNF-alph
38 bility to MCMV infection, demonstrating that translational arrest dependent on GCN2 contributes to th
39  the PTC also remotely inhibit PTC and cause translational arrest depending on the synthesized polype
40              It is, however, not involved in translational arrest during VHSV infection.
41 uld regulate the duration of stress- induced translational arrest in cells recovering from environmen
42   Formation of IB granules does not indicate translational arrest in the infected cells.
43 3 coat through YidC by obtaining a series of translational arrested intermediates, and investigate th
44                                              Translational arrest is a common antiviral strategy used
45                               Stress-induced translational arrest is observed in cells expressing a n
46 resource of human short-lived proteins under translational arrest, leading to untapped avenues of pro
47                                       Such a translational arrest may mediate overall adaptation of c
48 l for viral pathogenesis, where it precludes translational arrest mediated by double-stranded-RNA-dep
49 t leads to stress granule (SG) formation and translational arrest mediated by the phosphorylation of
50                                Despite this, translational arrest occurs during RVFV infection by unk
51                                              Translational arrest of 5'-TOPs via 4EBP1/2 restricts RV
52    We also show that this event leads to the translational arrest of ORF1a and S mRNAs in a manner de
53 lly predisposed persons could lead to global translational arrest of physiologically relevant enzymes
54 ' untranslated region of the M mRNA leads to translational arrest of the mRNA.
55                                      Uniform translational arrest of the nascent chains is achieved u
56 orce profile analysis (FPA)-a method where a translational arrest peptide (AP) engineered into the po
57                                              Translational arrest peptides (APs) are short stretches
58                         The counterintuitive translational arrest provided by tRNA cleavage may subve
59 y (A) stretches induce ribosome stalling and translational arrest through electrostatic interactions
60 conserved homeostatic response that mediates translational arrest through phosphorylation of eukaryot
61 .5-null virus to counteract the induction of translational arrest through the PKR antiviral pathway,
62  modulate the rate of translation and induce translational arrest to regulate expression of downstrea
63 n consensus sequences in a specific state of translational arrest with extended ribosome-protected fr
64                 These interactions can cause translational arrest with notable physiological conseque