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Interactions between the HIV-1 unspliced mRNA and host mRNA decay machineries
(MDPI AG, 2016)
© 2016 by the authors; licensee MDPI, Basel, Switzerland. The human immunodeficiency virus type-1 (HIV-1) unspliced transcript is used both as mRNA for the synthesis of structural proteins and as the packaged genome. Given ...
TMV induces RNA decay pathways to modulate gene silencing and disease symptoms
(Wiley Blackwell Publishing, Inc, 2017-01)
RNA decay pathways comprise a combination of RNA degradation mechanisms that are implicated in gene expression, development and defense responses in eukaryotes. These mechanisms are known as the RNA Quality Control or RQC ...
TMV induces RNA decay pathways to modulate gene silencing and disease symptoms
(2017)
RNA decay pathways comprise a combination of RNA degradation mechanisms that are implicated in gene expression, development and defense responses in eukaryotes. These mechanisms are known as the RNA Quality Control or RQC ...
Composition and function of P bodies in Arabidopsis thaliana
(Frontiers Media S.A., 2018)
Viral silencing suppressors and cellular proteins partner with plant RRP6-like exoribonucleases
(Springer, 2020-10)
RNA silencing and RNA decay are functionally interlaced, regulate gene expression and play a pivotal role in antiviral responses. As a counter defensive strategy, many plant and mammalian viruses encode suppressors which ...
Footprints of a trypanosomatid RNA world: pre-small subunit rRNA processing by spliced leader addition trans-splicing
(FUNDACO OSWALDO CRUZRIO DE JANEIRO, 2013-08-02)
The addition of a capped mini-exon [spliced leader (SL)] through trans-splicing is essential for the maturation of RNA polymerase (pol) II-transcribed polycistronic pre-mRNAs in all members of the Trypanosomatidae family. ...
Carpenter Syndrome: Extended RAB23 Mutation Spectrum and Analysis of Nonsense-mediated mRNA Decay
(WILEY-BLACKWELL, 2011)
Carpenter syndrome, a rare autosomal recessive disorder characterized by a combination of craniosynostosis, polysyndactyly, obesity, and other congenital malformations, is caused by mutations in RAB23, encoding a member ...