RNA-responsive elements for eukaryotic translational control
暂无分享,去创建一个
Evan M. Zhao | Emma J. Chory | Angelo S. Mao | David B. Thompson | J. Collins | Helena de Puig | F. Ran | Nathaniel D. Tippens | Max A. English | Eric S Zigon | Crystal Oh | P. Nguyen | P. Ramesh | Kehan Zhang | Xiao Tan | Isaac Han | Tiffany Y Hua | J. Collins | David B. Thompson
[1] G. Brewer,et al. IRES-targeting small molecule inhibits enterovirus 71 replication via allosteric stabilization of a ternary complex , 2020, Nature Communications.
[2] I. Bosch,et al. Serotype-specific detection of dengue viruses in a nonstructural protein 1-based enzyme-linked immunosorbent assay validated with a multi-national cohort , 2020, PLoS neglected tropical diseases.
[3] N. Grigorieff,et al. mRNA stem-loops can pause the ribosome by hindering A-site tRNA binding , 2020, bioRxiv.
[4] M. Farzan,et al. A reversible RNA on-switch that controls gene expression of AAV-delivered therapeutics in vivo , 2019, Nature Biotechnology.
[5] Peng Yin,et al. De-Novo-Designed Translation-Repressing Riboregulators for Multi-Input Cellular Logic , 2019, Nature chemical biology.
[6] Y. Harada,et al. HCV IRES Captures an Actively Translating 80S Ribosome. , 2019, Molecular cell.
[7] Niles A. Pierce,et al. Conditional Guide RNAs: Programmable Conditional Regulation of CRISPR/Cas Function in Bacterial and Mammalian Cells via Dynamic RNA Nanotechnology , 2019, ACS central science.
[8] Daniel G. Anderson,et al. RNA Circularization Diminishes Immunogenicity and Can Extend Translation Duration In Vivo. , 2019, Molecular cell.
[9] Allen P. Liu,et al. A Novel Synthetic Toehold Switch for MicroRNA Detection in Mammalian Cells. , 2019, ACS synthetic biology.
[10] S. Jaffrey,et al. Highly efficient expression of circular RNA aptamers in cells using autocatalytic transcripts , 2019, Nature Biotechnology.
[11] Ka-Hei Siu,et al. Riboregulated toehold-gated gRNA for programmable CRISPR–Cas9 function , 2018, Nature Chemical Biology.
[12] Jared E. Toettcher,et al. Optogenetic regulation of engineered cellular metabolism for microbial chemical production , 2018, Nature.
[13] S. Horner,et al. A Fluorescent Cell-Based System for Imaging Zika Virus Infection in Real-Time , 2018, Viruses.
[14] Daniel Olson,et al. Rapid antigen tests for dengue virus serotypes and Zika virus in patient serum , 2017, Science Translational Medicine.
[15] A. Ogawa,et al. Artificial OFF-Riboswitches That Downregulate Internal Ribosome Entry without Hybridization Switches in a Eukaryotic Cell-Free Translation System. , 2017, ACS synthetic biology.
[16] M. Farzan,et al. Rational design of aptazyme riboswitches for efficient control of gene expression in mammalian cells , 2016, eLife.
[17] Michele Felletti,et al. Twister ribozymes as highly versatile expression platforms for artificial riboswitches , 2016, Nature Communications.
[18] J. Murray,et al. Structural characterization of ribosome recruitment and translocation by type IV IRES , 2016, eLife.
[19] J. Kieft,et al. A dynamic RNA loop in an IRES affects multiple steps of elongation factor-mediated translation initiation , 2015, eLife.
[20] H. Noller,et al. Initiation of Translation in Bacteria by a Structured Eukaryotic IRES RNA , 2015, Nature.
[21] J. Collins,et al. Toehold Switches: De-Novo-Designed Regulators of Gene Expression , 2014, Cell.
[22] M. Jewett,et al. Characterizing IGR IRES-mediated translation initiation for use in yeast cell-free protein synthesis. , 2014, New biotechnology.
[23] G. Skavdis,et al. Comparative analysis of internal ribosomal entry sites as molecular tools for bicistronic expression. , 2014, Journal of biotechnology.
[24] M. Schnare,et al. A simple and fast system for cloning influenza A virus gene segments into pHW2000- and pCAGGS-based vectors , 2013, Archives of Virology.
[25] J. Muñoz-Jordán,et al. Dengue Virus: Isolation, Propagation, Quantification, and Storage , 2012, Current protocols in microbiology.
[26] O. Bensaude,et al. Inhibiting eukaryotic transcription. Which compound to choose? How to evaluate its activity? , 2011, Transcription.
[27] Jianyu Zhu,et al. Crystal structures of complexes containing domains from two viral internal ribosome entry site (IRES) RNAs bound to the 70S ribosome , 2011, Proceedings of the National Academy of Sciences.
[28] P. Yaswen,et al. A Versatile Viral System for Expression and Depletion of Proteins in Mammalian Cells , 2009, PloS one.
[29] N. Nakashima,et al. Binding Mode of the First Aminoacyl-tRNA in Translation Initiation Mediated by Plautia stali Intestine Virus Internal Ribosome Entry Site* , 2007, Journal of Biological Chemistry.
[30] P. Sarnow,et al. Enterovirus 71 contains a type I IRES element that functions when eukaryotic initiation factor eIF4G is cleaved. , 2003, Virology.
[31] Norihiro Shibuya,et al. Structural elements in the internal ribosome entry site of Plautia stali intestine virus responsible for binding with ribosomes. , 2003, Nucleic acids research.
[32] M. Niepmann,et al. Interaction of Translation Initiation Factor eIF4B with the Poliovirus Internal Ribosome Entry Site , 2002, Journal of Virology.
[33] Y. Kanamori,et al. A tertiary structure model of the internal ribosome entry site (IRES) for methionine-independent initiation of translation. , 2001, RNA.
[34] R. Webster,et al. "Ambisense" approach for the generation of influenza A virus: vRNA and mRNA synthesis from one template. , 2000, Virology.
[35] M. Nomura,et al. RNA polymerase switch in transcription of yeast rDNA: role of transcription factor UAF (upstream activation factor) in silencing rDNA transcription by RNA polymerase II. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[36] Y. Nogi,et al. Multiprotein transcription factor UAF interacts with the upstream element of the yeast RNA polymerase I promoter and forms a stable preinitiation complex. , 1996, Genes & development.
[37] V. Sandig,et al. A phage T7 class-III promoter functions as a polymerase II promoter in mammalian cells. , 1993, Gene.