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| Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
|---|---|---|---|---|---|---|---|
| Critical functions and key interactions mediated by the RNase E scaffolding domain in Pseudomonas aeruginosa | PLOS genetics |  | 2025 | 87 | 23 | ||
| Intrinsically disordered regions regulate RhlE RNA helicase functions in bacteria | Nucleic acids research | | 2024 | 143 | 85 | ||
| Formative assessments during COVID-19 pandemic: an observational study on performance and experiences of medical students | MedEdPublish | | 2023 | 97 | 195 | ||
| Mechanism of inhibition of bacterial RNA helicases by diazo dyes and implications for antimicrobial drug development | Biochemical pharmacology | | 2022 | 257 | 156 | ||
| RNase J1 and J2 are host-encoded factors for plasmid replication | Frontiers in Microbiology | | 2021 | 231 | 92 | ||
| The DEAD-box RNA helicase RhlE2 is a global regulator of Pseudomonas aeruginosa lifestyle and pathogenesis | Nucleic acids research | | 2021 | 215 | 162 | ||
| Auxiliary domains of the HrpB bacterial DExH-box helicase shape its RNA preferences | RNA Biology | | 2020 | 334 | 189 | ||
| Both exo- and endo-nucleolytic activities of RNase J1 from Staphylococcus aureus are manganese dependent and active on triphosphorylated 5'-ends | RNA biology |  | 2017 | 578 | 3 | ||
| Bacterial versatility requires DEAD-box RNA helicases | FEMS microbiology reviews | | 2015 | 686 | 4 | ||
| The C-terminal region of the RNA helicase CshA is required for the interaction with the degradosome and turnover of bulk RNA in the opportunistic pathogen Staphylococcus aureus | RNA biology | | 2015 | 666 | 1,488 | ||
| TRIM5 is an innate immune sensor for the retrovirus capsid lattice | Nature | | 2011 | 511 | 1 | ||
| Short double-stranded RNAs with an overhanging 5' ppp-nucleotide, as found in arenavirus genomes, act as RIG-I decoys | The Journal of biological chemistry | | 2011 | 637 | 0 | ||
| The double-stranded RNA binding domain of the vaccinia virus E3L protein inhibits both RNA- and DNA-induced activation of interferon beta | The Journal of biological chemistry | | 2009 | 684 | 0 | ||
| Genetic and biochemical analysis of yeast and human cap trimethylguanosine synthase: functional overlap of 2,2,7-trimethylguanosine caps, small nuclear ribonucleoprotein components, pre-mRNA splicing factors, and RNA decay pathways | The Journal of biological chemistry | | 2008 | 616 | 0 | ||
| RIG-I and dsRNA-induced IFNbeta activation | PloS one | | 2008 | 663 | 296 | ||
| Sendai virus RNA polymerase scanning for mRNA start sites at gene junctions | Virology | | 2007 | 590 | 404 | ||
| Activation of the beta interferon promoter by unnatural Sendai virus infection requires RIG-I and is inhibited by viral C proteins | Journal of virology | | 2007 | 646 | 324 | ||
| Ambisense sendai viruses are inherently unstable but are useful to study viral RNA synthesis | Journal of virology | | 2002 | 619 | 486 | ||
| The versatility of paramyxovirus RNA polymerase stuttering | Journal of virology | | 1999 | 617 | 249 | ||
| Two nucleotides immediately upstream of the essential A6G3 slippery sequence modulate the pattern of G insertions during Sendai virus mRNA editing | Journal of virology | | 1999 | 513 | 214 | ||
| Paramyxovirus RNA synthesis and the requirement for hexamer genome length: the rule of six revisited | Journal of virology | | 1998 | 601 | 480 | ||
| Sendai viruses with altered P, V, and W protein expression | Virology | | 1998 | 685 | 463 | ||
| Normal cellular replication of Sendai virus without the trans-frame, nonstructural V protein | Virology | | 1997 | 637 | 281 | ||
| Inhibition of Sendai virus genome replication due to promoter-increased selectivity: a possible role for the accessory C proteins | Journal of Virology | | 1997 | 302 | 132 |
