| RNase E resolves toxic condensates by counteracting phase separation of Type II RhlB helicases | Nucleic acids research |  | | 2026 | 19 | 27 |
|
| Critical functions and key interactions mediated by the RNase E scaffolding domain in Pseudomonas aeruginosa | PLOS genetics | | | 2025 | 161 | 92 |
|
| Intrinsically disordered regions regulate RhlE RNA helicase functions in bacteria | Nucleic acids research | | | 2024 | 178 | 132 |
|
| Formative assessments during COVID-19 pandemic: an observational study on performance and experiences of medical students | MedEdPublish | | | 2023 | 112 | 356 |
|
| Mechanism of inhibition of bacterial RNA helicases by diazo dyes and implications for antimicrobial drug development | Biochemical pharmacology | | | 2022 | 272 | 292 |
|
| RNase J1 and J2 are host-encoded factors for plasmid replication | Frontiers in Microbiology | | | 2021 | 245 | 117 |
|
| The DEAD-box RNA helicase RhlE2 is a global regulator of Pseudomonas aeruginosa lifestyle and pathogenesis | Nucleic acids research | | | 2021 | 234 | 292 |
|
| Auxiliary domains of the HrpB bacterial DExH-box helicase shape its RNA preferences | RNA Biology | | | 2020 | 353 | 326 |
|
| Both exo- and endo-nucleolytic activities of RNase J1 from Staphylococcus aureus are manganese dependent and active on triphosphorylated 5'-ends | RNA biology |  | | 2017 | 604 | 3 |
|
| Bacterial versatility requires DEAD-box RNA helicases | FEMS microbiology reviews | | | 2015 | 704 | 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 | 687 | 1,709 |
|
| TRIM5 is an innate immune sensor for the retrovirus capsid lattice | Nature | | | 2011 | 539 | 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 | 657 | 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 | 700 | 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 | 634 | 0 |
|
| RIG-I and dsRNA-induced IFNbeta activation | PloS one | | | 2008 | 683 | 381 |
|
| Sendai virus RNA polymerase scanning for mRNA start sites at gene junctions | Virology | | | 2007 | 606 | 584 |
|
| 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 | 674 | 445 |
|
| Ambisense sendai viruses are inherently unstable but are useful to study viral RNA synthesis | Journal of virology | | | 2002 | 635 | 629 |
|
| The versatility of paramyxovirus RNA polymerase stuttering | Journal of virology | | | 1999 | 640 | 519 |
|
| 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 | 529 | 318 |
|
| Paramyxovirus RNA synthesis and the requirement for hexamer genome length: the rule of six revisited | Journal of virology | | | 1998 | 622 | 1,205 |
|
| Sendai viruses with altered P, V, and W protein expression | Virology | | | 1998 | 710 | 500 |
|
| Normal cellular replication of Sendai virus without the trans-frame, nonstructural V protein | Virology | | | 1997 | 654 | 390 |
|
| Inhibition of Sendai virus genome replication due to promoter-increased selectivity: a possible role for the accessory C proteins | Journal of Virology | | | 1997 | 314 | 221 |
|
