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Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
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Intrinsically disordered regions regulate RhlE RNA helicase functions in bacteria | Nucleic acids research | 2024 | 38 | 20 | |||
Formative assessments during COVID-19 pandemic: an observational study on performance and experiences of medical students | MedEdPublish | 2023 | 38 | 26 | |||
Mechanism of inhibition of bacterial RNA helicases by diazo dyes and implications for antimicrobial drug development | Biochemical pharmacology | 2022 | 186 | 90 | |||
RNase J1 and J2 are host-encoded factors for plasmid replication | Frontiers in Microbiology | 2021 | 167 | 69 | |||
The DEAD-box RNA helicase RhlE2 is a global regulator of Pseudomonas aeruginosa lifestyle and pathogenesis | Nucleic acids research | 2021 | 146 | 90 | |||
Auxiliary domains of the HrpB bacterial DExH-box helicase shape its RNA preferences | RNA Biology | 2020 | 278 | 164 | |||
Both exo- and endo-nucleolytic activities of RNase J1 from Staphylococcus aureus are manganese dependent and active on triphosphorylated 5'-ends | RNA biology | 2017 | 518 | 3 | |||
Bacterial versatility requires DEAD-box RNA helicases | FEMS microbiology reviews | 2015 | 636 | 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 | 602 | 1 405 | |||
TRIM5 is an innate immune sensor for the retrovirus capsid lattice | Nature | 2011 | 447 | 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 | 580 | 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 | 620 | 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 | 555 | 0 | |||
RIG-I and dsRNA-induced IFNbeta activation | PloS one | 2008 | 592 | 264 | |||
Sendai virus RNA polymerase scanning for mRNA start sites at gene junctions | Virology | 2007 | 524 | 343 | |||
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 | 596 | 277 | |||
Ambisense sendai viruses are inherently unstable but are useful to study viral RNA synthesis | Journal of virology | 2002 | 534 | 404 | |||
The versatility of paramyxovirus RNA polymerase stuttering | Journal of virology | 1999 | 536 | 188 | |||
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 | 461 | 169 | |||
Paramyxovirus RNA synthesis and the requirement for hexamer genome length: the rule of six revisited | Journal of virology | 1998 | 533 | 320 | |||
Sendai viruses with altered P, V, and W protein expression | Virology | 1998 | 624 | 436 | |||
Normal cellular replication of Sendai virus without the trans-frame, nonstructural V protein | Virology | 1997 | 544 | 251 | |||
Inhibition of Sendai virus genome replication due to promoter-increased selectivity: a possible role for the accessory C proteins | Journal of Virology | 1997 | 255 | 113 |