42 results on '"Hausmann, Stéphane"'
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2. Formative assessments during COVID-19 pandemic: an observational study on performance and experiences of medical students
3. Mechanism of inhibition of bacterial RNA helicases by diazo dyes and implications for antimicrobial drug development
4. Cotranscriptional Paramyxovirus mRNA Editing: a Contradiction in Terms?
5. The DEAD-box RNA helicase RhlE2 is a global regulator ofPseudomonas aeruginosalifestyle and pathogenesis
6. RNase J1 and J2 Are Host-Encoded Factors for Plasmid Replication
7. The DEAD-box RNA helicases RhlE2 is a global regulator ofPseudomonas aeruginosalifestyle and pathogenesis
8. Auxiliary domains of the HrpB bacterial DExH-box helicase shape its RNA preferences
9. Both exo- and endo-nucleolytic activities of RNase J1 from Staphylococcus aureus are manganese dependent and active on triphosphorylated 5′-ends
10. 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 pathogenStaphylococcus aureus
11. Bacterial versatility requires DEAD-box RNA helicases
12. TRIM5α associates with proteasomal subunits in cells while in complex with HIV-1 virions
13. TRIM5 is an innate immune sensor for the retrovirus capsid lattice
14. Short Double-stranded RNAs with an Overhanging 5′ ppp-Nucleotide, as Found in Arenavirus Genomes, Act as RIG-I Decoys
15. The Double-stranded RNA Binding Domain of the Vaccinia Virus E3L Protein Inhibits Both RNA- and DNA-induced Activation of Interferon β
16. RIG-I and dsRNA-Induced IFNβ Activation
17. Genetic and Biochemical Analysis of Yeast and Human Cap Trimethylguanosine Synthase
18. Activation of the Beta Interferon Promoter by Unnatural Sendai Virus Infection Requires RIG-I and Is Inhibited by Viral C Proteins
19. Sendai virus RNA polymerase scanning for mRNA start sites at gene junctions
20. Mutational Analysis of Encephalitozoon cuniculi mRNA Cap (Guanine-N7) Methyltransferase, Structure of the Enzyme Bound to Sinefungin, and Evidence That Cap Methyltransferase Is the Target of Sinefungin's Antifungal Activity
21. Poxvirus mRNA Cap Methyltransferase
22. Fcp1 directly recognizes the C-terminal domain (CTD) and interacts with a site on RNA polymerase II distinct from the CTD
23. Giardia lamblia RNA Cap Guanine-N2 Methyltransferase (Tgs2)
24. Encephalitozoon cuniculi mRNA Cap (Guanine N-7) Methyltransferase
25. Yeast-like mRNA Capping Apparatus in Giardia lamblia
26. Specificity and Mechanism of RNA Cap Guanine-N2 Methyltransferase (Tgs1)
27. Arabidopsis C-terminal domain phosphatase-like 1 and 2 are essential Ser-5-specific C-terminal domain phosphatases
28. An Encephalitozoon cuniculi Ortholog of the RNA Polymerase II Carboxyl-Terminal Domain (CTD) Serine Phosphatase Fcp1
29. Schizosaccharomyces pombe Carboxyl-terminal Domain (CTD) Phosphatase Fcp1
30. Structure and Mechanism of mRNA Cap (Guanine-N7) Methyltransferase
31. Homodimeric Quaternary Structure Is Required for the in Vivo Function and Thermal Stability of Saccharomyces cerevisiae and Schizosaccharomyces pombe RNA Triphosphatases
32. Defining the Active Site of Schizosaccharomyces pombeC-terminal Domain Phosphatase Fcp1
33. Ambisense Sendai Viruses Are Inherently Unstable but Are Useful To Study Viral RNA Synthesis
34. Characterization of the CTD Phosphatase Fcp1 from Fission Yeast
35. Characterization of the mRNA Capping Apparatus of the Microsporidian Parasite Encephalitozoon cuniculi
36. An Essential Function of Saccharomyces cerevisiae RNA Triphosphatase Cet1 Is to Stabilize RNA Guanylyltransferase Ceg1 against Thermal Inactivation
37. The Length, Phosphorylation State, and Primary Structure of the RNA Polymerase II Carboxyl-terminal Domain Dictate Interactions with mRNA Capping Enzymes
38. The Versatility of Paramyxovirus RNA Polymerase Stuttering
39. Two Nucleotides Immediately Upstream of the Essential A 6 G 3 Slippery Sequence Modulate the Pattern of G Insertions during Sendai Virus mRNA Editing
40. Sendai Viruses with Altered P, V, and W Protein Expression
41. Paramyxovirus RNA Synthesis and the Requirement for Hexamer Genome Length: the Rule of Six Revisited
42. Normal Cellular Replication of Sendai Virus without thetrans-Frame, Nonstructural V Protein
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