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1 ch as transcription errors, mRNA damage, and translational frameshifting.
2  is recognized as 'slippery' and promotes -1 translational frameshifting.
3 ion of eukaryotic antizyme genes requires +1 translational frameshifting.
4  suggest the "out-of-frame pairing" model of translational frameshifting.
5 ion of IS6110 is thought to be controlled by translational frameshifting.
6 issociation causing premature termination or translational frameshifting.
7 ks known structural information required for translational frameshifting.
8 protein coding genes inferred as sites of +1 translational frameshifting.
9 s tau or as the shorter gamma that arises by translational frameshifting.
10  as a uniquely extreme example of programmed translational frameshifting.
11 orms: tau and the shorter gamma, produced by translational frameshifting.
12 ovided evidence diagnostic for +1 programmed translational frameshifting, a phenomenon disparately re
13 fting in vivo, we show that the induction of translational frameshifting also occurs under stressful
14 and forced overproduction of MiaA stimulated translational frameshifting and profoundly altered the E
15  this work suggests that CGG repeats support translational frameshifting and that chimeric RAN transl
16 uggest that expression of uncB is reduced by translational frameshifting and/or a translational false
17  coronaviruses, with polyprotein processing, translational frameshifting, and multiple sgRNA formatio
18 onal Lsi2 protein via transcriptional and/or translational frameshifting, and this limited amount of
19 t (gamma) forms generated through programmed translational frameshifting, but the need for both forms
20 that subvert standard decoding to program +1 translational frameshifting, either constitutively or in
21 omplex negative feedback system in which the translational frameshifting event may be viewed in engin
22                        BUD22 affected the +1 translational frameshifting event required to express th
23 omal genes are known to employ programmed +1 translational frameshifting for expression of full-lengt
24 logenetically diverse and extensive usage of translational frameshifting in animal mitochondrial codi
25 t there is a high frequency of programmed +1 translational frameshifting in ciliates of the Euplotes
26              A potential site for programmed translational frameshifting in ISMi1 was also identified
27 sm of gene regulation, the utilization of -1 translational frameshifting in regulating mammalian gene
28 tem-loop structure can significantly enhance translational frameshifting in the presence of the pepti
29 capsid-polymerase fusion protein produced by translational frameshifting in vivo may be due to specif
30                                              Translational frameshifting involves the repositioning o
31 f HmbR in DNM2 was found to be controlled by translational frameshifting involving a polyguanine (G)
32                                   Programmed translational frameshifting is a ubiquitous but rare mec
33                                              Translational frameshifting is a ubiquitous, if rare, fo
34                                   Programmed translational frameshifting is essential for the express
35                                 A programmed translational frameshifting mechanism similar to that us
36 effort to reconcile in vitro observations of translational frameshifting on Leishmania RNA virus 1-4
37 ple GGU-CAG-A, are also prone to significant translational frameshifting, suggesting the possibility
38 replication, discontinuous transcription and translational frameshifting, the alternative conformatio
39 e II (HTLV-2) use a similar mechanism for -1 translational frameshifting to overcome the termination
40                       Retroviruses employ -1 translational frameshifting to regulate the relative con
41               This is clearest in programmed translational frameshifting where the mRNA programs erra