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You searched for subject:(IRES RNA). Showing records 1 – 19 of 19 total matches.

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Virginia Tech

1. Wiley, Michael Ross. New tools for the study of virus-vector interactions in mosquitoes.

Degree: PhD, Entomology, 2012, Virginia Tech

 Mosquito-borne diseases continue to be a burden to global health. The viruses that cause these diseases are maintained in nature through a biological transmission cycle… (more)

Subjects/Keywords: IRES; B2; RNA-based immunity; alphavirus; mosquito

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APA (6th Edition):

Wiley, M. R. (2012). New tools for the study of virus-vector interactions in mosquitoes. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/77343

Chicago Manual of Style (16th Edition):

Wiley, Michael Ross. “New tools for the study of virus-vector interactions in mosquitoes.” 2012. Doctoral Dissertation, Virginia Tech. Accessed December 01, 2020. http://hdl.handle.net/10919/77343.

MLA Handbook (7th Edition):

Wiley, Michael Ross. “New tools for the study of virus-vector interactions in mosquitoes.” 2012. Web. 01 Dec 2020.

Vancouver:

Wiley MR. New tools for the study of virus-vector interactions in mosquitoes. [Internet] [Doctoral dissertation]. Virginia Tech; 2012. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10919/77343.

Council of Science Editors:

Wiley MR. New tools for the study of virus-vector interactions in mosquitoes. [Doctoral Dissertation]. Virginia Tech; 2012. Available from: http://hdl.handle.net/10919/77343


Indian Institute of Science

2. Bhat, Prasanna. Characterization of Host Protein Interactions with HCV RNA : Implications in Viral Translation, Replication and Design of Antivirals.

Degree: PhD, Faculty of Science, 2018, Indian Institute of Science

 HCV genome is a positive sense single-stranded RNA containing a single open reading frame (ORF) flanked by untranslated regions (UTRs), 5’UTR and 3’UTR.Initiation of HCV… (more)

Subjects/Keywords: Hepatitis C Virus (HCV) RNA; HCV RNA Host Protein Interactions; HVC Infection; HCV RNA Translation; HCV Genomes; HCV Replication; HCV IRES RNA; HCV IRES; HCV Replication; HCV-IRES; HCV-IRES; HCV RNA; Virus-Host Protein Interactions; Viral RNA Replication; Microbiology and Cell Biology

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APA (6th Edition):

Bhat, P. (2018). Characterization of Host Protein Interactions with HCV RNA : Implications in Viral Translation, Replication and Design of Antivirals. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/3496

Chicago Manual of Style (16th Edition):

Bhat, Prasanna. “Characterization of Host Protein Interactions with HCV RNA : Implications in Viral Translation, Replication and Design of Antivirals.” 2018. Doctoral Dissertation, Indian Institute of Science. Accessed December 01, 2020. http://etd.iisc.ac.in/handle/2005/3496.

MLA Handbook (7th Edition):

Bhat, Prasanna. “Characterization of Host Protein Interactions with HCV RNA : Implications in Viral Translation, Replication and Design of Antivirals.” 2018. Web. 01 Dec 2020.

Vancouver:

Bhat P. Characterization of Host Protein Interactions with HCV RNA : Implications in Viral Translation, Replication and Design of Antivirals. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2018. [cited 2020 Dec 01]. Available from: http://etd.iisc.ac.in/handle/2005/3496.

Council of Science Editors:

Bhat P. Characterization of Host Protein Interactions with HCV RNA : Implications in Viral Translation, Replication and Design of Antivirals. [Doctoral Dissertation]. Indian Institute of Science; 2018. Available from: http://etd.iisc.ac.in/handle/2005/3496


University of Manchester

3. Rasul, Usman Anawar. NMR studies of the structure, kinetics and interactions of the conserved RNA motifs in the FMDV IRES.

Degree: 2012, University of Manchester

 The structure, kinetics, and interactions of the conserved 16mer and 15mer RNA motifs of the internal ribosome entry site (IRES) of the Foot-and-Mouth Disease virus… (more)

Subjects/Keywords: FMDV; IRES; GNRA; RNA; NMR; Mg2+; 19F-NMR

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APA (6th Edition):

Rasul, U. A. (2012). NMR studies of the structure, kinetics and interactions of the conserved RNA motifs in the FMDV IRES. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:162954

Chicago Manual of Style (16th Edition):

Rasul, Usman Anawar. “NMR studies of the structure, kinetics and interactions of the conserved RNA motifs in the FMDV IRES.” 2012. Doctoral Dissertation, University of Manchester. Accessed December 01, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:162954.

MLA Handbook (7th Edition):

Rasul, Usman Anawar. “NMR studies of the structure, kinetics and interactions of the conserved RNA motifs in the FMDV IRES.” 2012. Web. 01 Dec 2020.

Vancouver:

Rasul UA. NMR studies of the structure, kinetics and interactions of the conserved RNA motifs in the FMDV IRES. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2020 Dec 01]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:162954.

Council of Science Editors:

Rasul UA. NMR studies of the structure, kinetics and interactions of the conserved RNA motifs in the FMDV IRES. [Doctoral Dissertation]. University of Manchester; 2012. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:162954


University of California – San Francisco

4. Xue, Shifeng. RNA regulons in Hox 5'UTRs confer ribosome specificity to gene regulation and embryonic development.

Degree: Developmental Biology, 2014, University of California – San Francisco

 Historically, the ribosome has been viewed as a ribozyme with constitutive rather than regulatory capacity in mRNA translation. However, emerging studies reveal that ribosome activity… (more)

Subjects/Keywords: Developmental biology; Molecular biology; embryology; Hox; IRES; ribosome; RNA regulation; translation

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APA (6th Edition):

Xue, S. (2014). RNA regulons in Hox 5'UTRs confer ribosome specificity to gene regulation and embryonic development. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/42h50712

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Xue, Shifeng. “RNA regulons in Hox 5'UTRs confer ribosome specificity to gene regulation and embryonic development.” 2014. Thesis, University of California – San Francisco. Accessed December 01, 2020. http://www.escholarship.org/uc/item/42h50712.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Xue, Shifeng. “RNA regulons in Hox 5'UTRs confer ribosome specificity to gene regulation and embryonic development.” 2014. Web. 01 Dec 2020.

Vancouver:

Xue S. RNA regulons in Hox 5'UTRs confer ribosome specificity to gene regulation and embryonic development. [Internet] [Thesis]. University of California – San Francisco; 2014. [cited 2020 Dec 01]. Available from: http://www.escholarship.org/uc/item/42h50712.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Xue S. RNA regulons in Hox 5'UTRs confer ribosome specificity to gene regulation and embryonic development. [Thesis]. University of California – San Francisco; 2014. Available from: http://www.escholarship.org/uc/item/42h50712

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Manchester

5. Rasul, Usman Anawar. NMR studies of the structure, kinetics and interactions of the conserved RNA motifs in the FMDV IRES.

Degree: PhD, 2012, University of Manchester

 The structure, kinetics, and interactions of the conserved 16mer and 15mer RNA motifs of the internal ribosome entry site (IRES) of the Foot-and-Mouth Disease virus… (more)

Subjects/Keywords: 636.089691; FMDV; IRES; GNRA; RNA; NMR; Mg2+; 19F-NMR

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APA (6th Edition):

Rasul, U. A. (2012). NMR studies of the structure, kinetics and interactions of the conserved RNA motifs in the FMDV IRES. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/nmr-studies-of-the-structure-kinetics-and-interactions-of-the-conserved-rna-motifs-in-the-fmdv-ires(be21f327-53e1-48aa-bf9c-c4bd2d028417).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.554174

Chicago Manual of Style (16th Edition):

Rasul, Usman Anawar. “NMR studies of the structure, kinetics and interactions of the conserved RNA motifs in the FMDV IRES.” 2012. Doctoral Dissertation, University of Manchester. Accessed December 01, 2020. https://www.research.manchester.ac.uk/portal/en/theses/nmr-studies-of-the-structure-kinetics-and-interactions-of-the-conserved-rna-motifs-in-the-fmdv-ires(be21f327-53e1-48aa-bf9c-c4bd2d028417).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.554174.

MLA Handbook (7th Edition):

Rasul, Usman Anawar. “NMR studies of the structure, kinetics and interactions of the conserved RNA motifs in the FMDV IRES.” 2012. Web. 01 Dec 2020.

Vancouver:

Rasul UA. NMR studies of the structure, kinetics and interactions of the conserved RNA motifs in the FMDV IRES. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2020 Dec 01]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/nmr-studies-of-the-structure-kinetics-and-interactions-of-the-conserved-rna-motifs-in-the-fmdv-ires(be21f327-53e1-48aa-bf9c-c4bd2d028417).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.554174.

Council of Science Editors:

Rasul UA. NMR studies of the structure, kinetics and interactions of the conserved RNA motifs in the FMDV IRES. [Doctoral Dissertation]. University of Manchester; 2012. Available from: https://www.research.manchester.ac.uk/portal/en/theses/nmr-studies-of-the-structure-kinetics-and-interactions-of-the-conserved-rna-motifs-in-the-fmdv-ires(be21f327-53e1-48aa-bf9c-c4bd2d028417).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.554174


Indian Institute of Science

6. Arandkar, Sharath Chandra. Characterization of the Cis and Trans Acting Factors that Influence p53 IRES Function.

Degree: PhD, Faculty of Science, 2018, Indian Institute of Science

 p53 is a nodal tumor suppressor protein that acts as a major defense against cancers. Approximately 50% of human tumours have mutations in p53 gene.… (more)

Subjects/Keywords: Tumor Supressor Protein p53; Cancer Therapy; p53 Internal Ribosome Entry Sites (IRES) Function; p53 RNA; IRES RNA; Annexin A2 - p53 IRES Function; PSF-Polypyrimidine Tract Binding Protein-Associated Splicing Factor; p53 Gene Expression - Regulation; p53 Mediated Apoptosis; Cis Acting Factors - p53 IRES Function; p53 IRES Function; p53 Isoforms; p53 mRNA; p53 IRES RNA; Molecular Biology

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APA (6th Edition):

Arandkar, S. C. (2018). Characterization of the Cis and Trans Acting Factors that Influence p53 IRES Function. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/3243

Chicago Manual of Style (16th Edition):

Arandkar, Sharath Chandra. “Characterization of the Cis and Trans Acting Factors that Influence p53 IRES Function.” 2018. Doctoral Dissertation, Indian Institute of Science. Accessed December 01, 2020. http://etd.iisc.ac.in/handle/2005/3243.

MLA Handbook (7th Edition):

Arandkar, Sharath Chandra. “Characterization of the Cis and Trans Acting Factors that Influence p53 IRES Function.” 2018. Web. 01 Dec 2020.

Vancouver:

Arandkar SC. Characterization of the Cis and Trans Acting Factors that Influence p53 IRES Function. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2018. [cited 2020 Dec 01]. Available from: http://etd.iisc.ac.in/handle/2005/3243.

Council of Science Editors:

Arandkar SC. Characterization of the Cis and Trans Acting Factors that Influence p53 IRES Function. [Doctoral Dissertation]. Indian Institute of Science; 2018. Available from: http://etd.iisc.ac.in/handle/2005/3243


University of California – San Diego

7. Boerneke, Mark A. Ligand-responsive RNA switches: viral translation regulators, therapeutic targets, and tunable building blocks for nanotechnology.

Degree: Chemistry, 2016, University of California – San Diego

 Ligand-responsive RNA mechanical switches represent a new class of simple and small switching modules which regulate viral translation initiation by adopting well-defined ligand-free and bound… (more)

Subjects/Keywords: Chemistry; Biochemistry; conformational switch; hepatitis C virus; IRES; RNA Switch; RNA virus; Self-assembling RNA nanostructures

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APA (6th Edition):

Boerneke, M. A. (2016). Ligand-responsive RNA switches: viral translation regulators, therapeutic targets, and tunable building blocks for nanotechnology. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/87h4z033

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Boerneke, Mark A. “Ligand-responsive RNA switches: viral translation regulators, therapeutic targets, and tunable building blocks for nanotechnology.” 2016. Thesis, University of California – San Diego. Accessed December 01, 2020. http://www.escholarship.org/uc/item/87h4z033.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Boerneke, Mark A. “Ligand-responsive RNA switches: viral translation regulators, therapeutic targets, and tunable building blocks for nanotechnology.” 2016. Web. 01 Dec 2020.

Vancouver:

Boerneke MA. Ligand-responsive RNA switches: viral translation regulators, therapeutic targets, and tunable building blocks for nanotechnology. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2020 Dec 01]. Available from: http://www.escholarship.org/uc/item/87h4z033.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Boerneke MA. Ligand-responsive RNA switches: viral translation regulators, therapeutic targets, and tunable building blocks for nanotechnology. [Thesis]. University of California – San Diego; 2016. Available from: http://www.escholarship.org/uc/item/87h4z033

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Indian Institute of Science

8. Verma, Bhupendra Kumar. Functional Characterization Of The Internal Ribosome Entry Site Of Coxsackievirus B3 RNA.

Degree: PhD, Faculty of Science, 2011, Indian Institute of Science

 CoxsackievirusB3 (CVB3), a member of the Picornaviridae family is the causative agent of Virus-induced Myocarditis and Dilated Cardiomyopathy. The 5’UTR contains an Internal Ribosome Entry… (more)

Subjects/Keywords: Ribosomes; Coxsackievirus B3; Ribonucleic Acid (RNA); RNA Viruses; Internal Ribosome Entry Site (IRES); Coxsackievirus B3 - Translation; Viruses - Reproduction; IRES Mediated Translation; Viral Proteins; Coxsackievirus B3 RNA Translation; CVB3; Cryptic AUG; Biochemical Genetics

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APA (6th Edition):

Verma, B. K. (2011). Functional Characterization Of The Internal Ribosome Entry Site Of Coxsackievirus B3 RNA. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/1278

Chicago Manual of Style (16th Edition):

Verma, Bhupendra Kumar. “Functional Characterization Of The Internal Ribosome Entry Site Of Coxsackievirus B3 RNA.” 2011. Doctoral Dissertation, Indian Institute of Science. Accessed December 01, 2020. http://etd.iisc.ac.in/handle/2005/1278.

MLA Handbook (7th Edition):

Verma, Bhupendra Kumar. “Functional Characterization Of The Internal Ribosome Entry Site Of Coxsackievirus B3 RNA.” 2011. Web. 01 Dec 2020.

Vancouver:

Verma BK. Functional Characterization Of The Internal Ribosome Entry Site Of Coxsackievirus B3 RNA. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2011. [cited 2020 Dec 01]. Available from: http://etd.iisc.ac.in/handle/2005/1278.

Council of Science Editors:

Verma BK. Functional Characterization Of The Internal Ribosome Entry Site Of Coxsackievirus B3 RNA. [Doctoral Dissertation]. Indian Institute of Science; 2011. Available from: http://etd.iisc.ac.in/handle/2005/1278


Penn State University

9. Origanti, Sofia S. Multiple mechanisms of ODC regulation by activated Ras: studies in an epithelial cell model .

Degree: 2008, Penn State University

 A majority of human cancers carry activating mutations in the Ras oncogene. One of the key effectors of Ras that is essential for its tumorigenic… (more)

Subjects/Keywords: eIF4E phsophoryaltion; IRES; ras; ODC; RNA stability

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APA (6th Edition):

Origanti, S. S. (2008). Multiple mechanisms of ODC regulation by activated Ras: studies in an epithelial cell model . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/7490

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Origanti, Sofia S. “Multiple mechanisms of ODC regulation by activated Ras: studies in an epithelial cell model .” 2008. Thesis, Penn State University. Accessed December 01, 2020. https://submit-etda.libraries.psu.edu/catalog/7490.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Origanti, Sofia S. “Multiple mechanisms of ODC regulation by activated Ras: studies in an epithelial cell model .” 2008. Web. 01 Dec 2020.

Vancouver:

Origanti SS. Multiple mechanisms of ODC regulation by activated Ras: studies in an epithelial cell model . [Internet] [Thesis]. Penn State University; 2008. [cited 2020 Dec 01]. Available from: https://submit-etda.libraries.psu.edu/catalog/7490.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Origanti SS. Multiple mechanisms of ODC regulation by activated Ras: studies in an epithelial cell model . [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/7490

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Indian Institute of Science

10. Shwetha, S. Host-Pathogen Interactions in Hepatitis C Virus Infection : Deciphering the Role of Host Proteins and MicroRNAs.

Degree: PhD, Faculty of Science, 2018, Indian Institute of Science

 Host-pathogen interactions in Hepatitis C Virus infection: Deciphering the role of host proteins and microRNAs Hepatitis C virus (HCV) is a positive sense single stranded… (more)

Subjects/Keywords: Hepatitis C Virus Infection; Micro RNAs - HCV Infection; RNA Viruses; Hepatitis C Virus Replication; Hepatitis C Virus (HCV) RNA Binding; Viral Proteins; Host Proteins-HCV Infection; Hepatitis C Virus Pathogenesis; Hepatitis C Virus-Internal Ribosomal Entry Site (HCV-IRES) Mediated Translation; Hepatitis C Virus Diagnosis and Therapy; HCV-RNA Translation; HCV - miRNA; HCV Replication; HCV IRES; HCV Pathogenesis; Microbiology and Cell Biology

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APA (6th Edition):

Shwetha, S. (2018). Host-Pathogen Interactions in Hepatitis C Virus Infection : Deciphering the Role of Host Proteins and MicroRNAs. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/3858

Chicago Manual of Style (16th Edition):

Shwetha, S. “Host-Pathogen Interactions in Hepatitis C Virus Infection : Deciphering the Role of Host Proteins and MicroRNAs.” 2018. Doctoral Dissertation, Indian Institute of Science. Accessed December 01, 2020. http://etd.iisc.ac.in/handle/2005/3858.

MLA Handbook (7th Edition):

Shwetha, S. “Host-Pathogen Interactions in Hepatitis C Virus Infection : Deciphering the Role of Host Proteins and MicroRNAs.” 2018. Web. 01 Dec 2020.

Vancouver:

Shwetha S. Host-Pathogen Interactions in Hepatitis C Virus Infection : Deciphering the Role of Host Proteins and MicroRNAs. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2018. [cited 2020 Dec 01]. Available from: http://etd.iisc.ac.in/handle/2005/3858.

Council of Science Editors:

Shwetha S. Host-Pathogen Interactions in Hepatitis C Virus Infection : Deciphering the Role of Host Proteins and MicroRNAs. [Doctoral Dissertation]. Indian Institute of Science; 2018. Available from: http://etd.iisc.ac.in/handle/2005/3858


Penn State University

11. Toroney, Rebecca. Investigating Roles of Unconventional RNA Primary, Secondary, and Tertiary Motifs in Regulation of the Protein Kinase PKR .

Degree: 2010, Penn State University

 Much is known about the importance of protein folding and structure in human health. Like protein, RNA is a biopolymer essential to cellular function that… (more)

Subjects/Keywords: Hepatitis C Virus; RNA-protein interactions; IRES; PKR; innate immunity; triphosphate

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APA (6th Edition):

Toroney, R. (2010). Investigating Roles of Unconventional RNA Primary, Secondary, and Tertiary Motifs in Regulation of the Protein Kinase PKR . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/11499

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Toroney, Rebecca. “Investigating Roles of Unconventional RNA Primary, Secondary, and Tertiary Motifs in Regulation of the Protein Kinase PKR .” 2010. Thesis, Penn State University. Accessed December 01, 2020. https://submit-etda.libraries.psu.edu/catalog/11499.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Toroney, Rebecca. “Investigating Roles of Unconventional RNA Primary, Secondary, and Tertiary Motifs in Regulation of the Protein Kinase PKR .” 2010. Web. 01 Dec 2020.

Vancouver:

Toroney R. Investigating Roles of Unconventional RNA Primary, Secondary, and Tertiary Motifs in Regulation of the Protein Kinase PKR . [Internet] [Thesis]. Penn State University; 2010. [cited 2020 Dec 01]. Available from: https://submit-etda.libraries.psu.edu/catalog/11499.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Toroney R. Investigating Roles of Unconventional RNA Primary, Secondary, and Tertiary Motifs in Regulation of the Protein Kinase PKR . [Thesis]. Penn State University; 2010. Available from: https://submit-etda.libraries.psu.edu/catalog/11499

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

12. Durie, Danielle. RNA Binding Protein HuR Regulates the Expression of Bcl-xL .

Degree: 2012, University of Ottawa

 The RNA-binding protein HuR controls key cellular processes by binding target mRNAs and regulating them at various post-transcriptional levels. HuR can function as an Internal… (more)

Subjects/Keywords: RNA binding protein; HuR; Bcl-xL; translation; IRES; Apoptosis; mitochondria

…ribosomal RNA which specifically impacts IRES-mediated translation. Yoon et al (2006)… …List of Figures Figure 1. Cap-dependent versus IRES-dependent translation initiation 9… …morphology through Bcl-xL 45 Figure 8. Secondary structure of the XIAP IRES and Bcl-xL 5’UTR 51… …Introduction 1.1 RNA-binding protein HuR The Hu family of RNA-binding proteins comprise HuB, HuC and… …many RNA-binding proteins (RBPs), HuR contains 3 RRMs, or RNA-recognition motifs… 

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APA (6th Edition):

Durie, D. (2012). RNA Binding Protein HuR Regulates the Expression of Bcl-xL . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/23206

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Durie, Danielle. “RNA Binding Protein HuR Regulates the Expression of Bcl-xL .” 2012. Thesis, University of Ottawa. Accessed December 01, 2020. http://hdl.handle.net/10393/23206.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Durie, Danielle. “RNA Binding Protein HuR Regulates the Expression of Bcl-xL .” 2012. Web. 01 Dec 2020.

Vancouver:

Durie D. RNA Binding Protein HuR Regulates the Expression of Bcl-xL . [Internet] [Thesis]. University of Ottawa; 2012. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10393/23206.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Durie D. RNA Binding Protein HuR Regulates the Expression of Bcl-xL . [Thesis]. University of Ottawa; 2012. Available from: http://hdl.handle.net/10393/23206

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Indian Institute of Science

13. Kumar, Anuj. Mechanistic Insights into Translation and Replication of Hepatitis C Virus RNA : Exploring Direct-Acting Antivirals.

Degree: PhD, Faculty of Science, 2018, Indian Institute of Science

 Hepatitis C virus (HCV), a blood-borne pathogen, is a small enveloped RNA virus belonging to the Hepacivirus genus of the Flaviviridae family. HCV infection represents… (more)

Subjects/Keywords: Hepatitis C Virus RNA; HCV Genotypes; HCV Vaccines; Hepatitis C Virus Infection; Antivirals; Human La Protein; Hepatitis C Virus Life Cycle; Viral Proteins; HCV Replication; HCV IRES; HCV Translation; HCV Infection; HCV Vaccine Development; Hepatitis C Virus (HCV); Microbiology and Cell Biology

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APA (6th Edition):

Kumar, A. (2018). Mechanistic Insights into Translation and Replication of Hepatitis C Virus RNA : Exploring Direct-Acting Antivirals. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/3260

Chicago Manual of Style (16th Edition):

Kumar, Anuj. “Mechanistic Insights into Translation and Replication of Hepatitis C Virus RNA : Exploring Direct-Acting Antivirals.” 2018. Doctoral Dissertation, Indian Institute of Science. Accessed December 01, 2020. http://etd.iisc.ac.in/handle/2005/3260.

MLA Handbook (7th Edition):

Kumar, Anuj. “Mechanistic Insights into Translation and Replication of Hepatitis C Virus RNA : Exploring Direct-Acting Antivirals.” 2018. Web. 01 Dec 2020.

Vancouver:

Kumar A. Mechanistic Insights into Translation and Replication of Hepatitis C Virus RNA : Exploring Direct-Acting Antivirals. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2018. [cited 2020 Dec 01]. Available from: http://etd.iisc.ac.in/handle/2005/3260.

Council of Science Editors:

Kumar A. Mechanistic Insights into Translation and Replication of Hepatitis C Virus RNA : Exploring Direct-Acting Antivirals. [Doctoral Dissertation]. Indian Institute of Science; 2018. Available from: http://etd.iisc.ac.in/handle/2005/3260


Indian Institute of Science

14. Ray, Upasana. Unravelling The Regulators Of Translation And Replication Of Hepatitis C Virus.

Degree: PhD, Faculty of Science, 2013, Indian Institute of Science

 Unravelling the regulators of translation and replication of Hepatitis C virus Hepatitis C virus (HCV) is a positive sense, single stranded RNA virus belonging to… (more)

Subjects/Keywords: Hepatitis C Virus (HCV); Hepatitis C Virus - Replication; HCV-NS3 Protein; Non-structural Protein 3; Human La Protein; HCV IRES; NS3 Protease; Hep C Viral Switch; Hepatitis C Viral RNA; NS3 Protein; Virology

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APA (6th Edition):

Ray, U. (2013). Unravelling The Regulators Of Translation And Replication Of Hepatitis C Virus. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/2032

Chicago Manual of Style (16th Edition):

Ray, Upasana. “Unravelling The Regulators Of Translation And Replication Of Hepatitis C Virus.” 2013. Doctoral Dissertation, Indian Institute of Science. Accessed December 01, 2020. http://etd.iisc.ac.in/handle/2005/2032.

MLA Handbook (7th Edition):

Ray, Upasana. “Unravelling The Regulators Of Translation And Replication Of Hepatitis C Virus.” 2013. Web. 01 Dec 2020.

Vancouver:

Ray U. Unravelling The Regulators Of Translation And Replication Of Hepatitis C Virus. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2013. [cited 2020 Dec 01]. Available from: http://etd.iisc.ac.in/handle/2005/2032.

Council of Science Editors:

Ray U. Unravelling The Regulators Of Translation And Replication Of Hepatitis C Virus. [Doctoral Dissertation]. Indian Institute of Science; 2013. Available from: http://etd.iisc.ac.in/handle/2005/2032


Georgia State University

15. Radu, Gertrud Ulrike. Functional Analyses of West Nile Virus (WNV) Bicistronic Replicons Containing Different Sequence Elements and of Simian Hemorrhagic Fever Virus (SHFV) Polyprotein Processing.

Degree: PhD, Biology, 2007, Georgia State University

  The flavivirus West Nile virus (WNV) encodes a single polyprotein that is processed into three structural and seven nonstructural proteins. Various WNV bicistronic replicons… (more)

Subjects/Keywords: Papain-like cysteine protease; West Nile virus; IRES; Capsid; Simian hemorrhagic fever virus; Translation; RNA Replication; Replicon; Biology

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APA (6th Edition):

Radu, G. U. (2007). Functional Analyses of West Nile Virus (WNV) Bicistronic Replicons Containing Different Sequence Elements and of Simian Hemorrhagic Fever Virus (SHFV) Polyprotein Processing. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/biology_diss/85

Chicago Manual of Style (16th Edition):

Radu, Gertrud Ulrike. “Functional Analyses of West Nile Virus (WNV) Bicistronic Replicons Containing Different Sequence Elements and of Simian Hemorrhagic Fever Virus (SHFV) Polyprotein Processing.” 2007. Doctoral Dissertation, Georgia State University. Accessed December 01, 2020. https://scholarworks.gsu.edu/biology_diss/85.

MLA Handbook (7th Edition):

Radu, Gertrud Ulrike. “Functional Analyses of West Nile Virus (WNV) Bicistronic Replicons Containing Different Sequence Elements and of Simian Hemorrhagic Fever Virus (SHFV) Polyprotein Processing.” 2007. Web. 01 Dec 2020.

Vancouver:

Radu GU. Functional Analyses of West Nile Virus (WNV) Bicistronic Replicons Containing Different Sequence Elements and of Simian Hemorrhagic Fever Virus (SHFV) Polyprotein Processing. [Internet] [Doctoral dissertation]. Georgia State University; 2007. [cited 2020 Dec 01]. Available from: https://scholarworks.gsu.edu/biology_diss/85.

Council of Science Editors:

Radu GU. Functional Analyses of West Nile Virus (WNV) Bicistronic Replicons Containing Different Sequence Elements and of Simian Hemorrhagic Fever Virus (SHFV) Polyprotein Processing. [Doctoral Dissertation]. Georgia State University; 2007. Available from: https://scholarworks.gsu.edu/biology_diss/85

16. Ross, Martin James. Investigation into Catalytic Metallodrugs that Target Hepatitis C IRES RNA: Development, Characterization, and Mechanism.

Degree: PhD, Chemistry, 2015, The Ohio State University

 Metals have been used for therapeutic purposes since the dawn of civilization including the ancient Egyptians using copper jars to sterilize their water. This use… (more)

Subjects/Keywords: Chemistry; RNA oxidation; ATCUN; SLIIb; SLIV; HCV; IRES; 5 NTR; Cu; Ni; Pd; Pt; Au; Co

…IIb of hepatitis C IRES RNA.” ChemMedChem. 2014, 9, 1275-1285. Fields of Study Major Field… …Metallodrugs Targeting Stem Loop IIb of Hepatitis C IRES RNA .................................. 31… …with an In-depth Characterization of Mechanism with GGHYrFK-Cu with HCV SLIIb IRES RNA… …171 Chapter 5: Catalytic Metallodrugs Based on the LaR2C Peptide Target HCV SLIV IRES RNA… …40 2.4.3 RNA Cleavage Reactivity… 

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APA (6th Edition):

Ross, M. J. (2015). Investigation into Catalytic Metallodrugs that Target Hepatitis C IRES RNA: Development, Characterization, and Mechanism. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1440421045

Chicago Manual of Style (16th Edition):

Ross, Martin James. “Investigation into Catalytic Metallodrugs that Target Hepatitis C IRES RNA: Development, Characterization, and Mechanism.” 2015. Doctoral Dissertation, The Ohio State University. Accessed December 01, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1440421045.

MLA Handbook (7th Edition):

Ross, Martin James. “Investigation into Catalytic Metallodrugs that Target Hepatitis C IRES RNA: Development, Characterization, and Mechanism.” 2015. Web. 01 Dec 2020.

Vancouver:

Ross MJ. Investigation into Catalytic Metallodrugs that Target Hepatitis C IRES RNA: Development, Characterization, and Mechanism. [Internet] [Doctoral dissertation]. The Ohio State University; 2015. [cited 2020 Dec 01]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1440421045.

Council of Science Editors:

Ross MJ. Investigation into Catalytic Metallodrugs that Target Hepatitis C IRES RNA: Development, Characterization, and Mechanism. [Doctoral Dissertation]. The Ohio State University; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1440421045


Indian Institute of Science

17. Grover, Richa. Translational Control Of p53 And Its Isoform By Internal Initiation.

Degree: PhD, Faculty of Science, 2010, Indian Institute of Science

 Tumor suppressor p53, the guardian of the genome, has been intensely studied molecule owing to its central role in maintaining cellular integrity. While the level… (more)

Subjects/Keywords: Ribonucleic Acid (RNA); Proteins; RNA Viruses; p53 Protein; p53 Protein Isoforms; p53 RNA - Structural Analysis; Protein Translation; Polypyrimidine Tract Binding Protein; Protein Regulation; IRES RNA; PTB Binding; p53 mRNA; Biochemical Genetics

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APA (6th Edition):

Grover, R. (2010). Translational Control Of p53 And Its Isoform By Internal Initiation. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/764

Chicago Manual of Style (16th Edition):

Grover, Richa. “Translational Control Of p53 And Its Isoform By Internal Initiation.” 2010. Doctoral Dissertation, Indian Institute of Science. Accessed December 01, 2020. http://etd.iisc.ac.in/handle/2005/764.

MLA Handbook (7th Edition):

Grover, Richa. “Translational Control Of p53 And Its Isoform By Internal Initiation.” 2010. Web. 01 Dec 2020.

Vancouver:

Grover R. Translational Control Of p53 And Its Isoform By Internal Initiation. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2010. [cited 2020 Dec 01]. Available from: http://etd.iisc.ac.in/handle/2005/764.

Council of Science Editors:

Grover R. Translational Control Of p53 And Its Isoform By Internal Initiation. [Doctoral Dissertation]. Indian Institute of Science; 2010. Available from: http://etd.iisc.ac.in/handle/2005/764

18. 谷脇, 琢也; タニワキ, タクヤ. 可変型遺伝子トラップベクターpU-17を用いたトラップラインの樹立と解析 : カヘンガタ イデンシ トラップ ベクター pU-17 オ モチイタ トラップ ライン ノ ジュリツ ト カイセキ; Characterization of an exchangeable gene trap using pU-17 carrying a stop codon-βgeo cassette.

Degree: Kumamoto University / 熊本大学

 We have developed a new exchangeable gene trap vector, pU-17, carrying the intron-lox71-splicing acceptor (SA)-βgeo-loxP-pA-lox2272-pSP73-lox511. The SA contains three stop codons in-frame with the ATG… (more)

Subjects/Keywords: エレクトロポレーション; genomic DNA; RNA解析; キメラマウス; splice acceptor(SA); Cre-mutant lox system; enchanged green fluorescent protein(EGFP)遺伝; internal ribosomal entry site(IRES)

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APA (6th Edition):

谷脇, 琢也; タニワキ, . (n.d.). 可変型遺伝子トラップベクターpU-17を用いたトラップラインの樹立と解析 : カヘンガタ イデンシ トラップ ベクター pU-17 オ モチイタ トラップ ライン ノ ジュリツ ト カイセキ; Characterization of an exchangeable gene trap using pU-17 carrying a stop codon-βgeo cassette. (Thesis). Kumamoto University / 熊本大学. Retrieved from http://hdl.handle.net/2298/11144

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

谷脇, 琢也; タニワキ, タクヤ. “可変型遺伝子トラップベクターpU-17を用いたトラップラインの樹立と解析 : カヘンガタ イデンシ トラップ ベクター pU-17 オ モチイタ トラップ ライン ノ ジュリツ ト カイセキ; Characterization of an exchangeable gene trap using pU-17 carrying a stop codon-βgeo cassette.” Thesis, Kumamoto University / 熊本大学. Accessed December 01, 2020. http://hdl.handle.net/2298/11144.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

谷脇, 琢也; タニワキ, タクヤ. “可変型遺伝子トラップベクターpU-17を用いたトラップラインの樹立と解析 : カヘンガタ イデンシ トラップ ベクター pU-17 オ モチイタ トラップ ライン ノ ジュリツ ト カイセキ; Characterization of an exchangeable gene trap using pU-17 carrying a stop codon-βgeo cassette.” Web. 01 Dec 2020.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

谷脇, 琢也; タニワキ . 可変型遺伝子トラップベクターpU-17を用いたトラップラインの樹立と解析 : カヘンガタ イデンシ トラップ ベクター pU-17 オ モチイタ トラップ ライン ノ ジュリツ ト カイセキ; Characterization of an exchangeable gene trap using pU-17 carrying a stop codon-βgeo cassette. [Internet] [Thesis]. Kumamoto University / 熊本大学; [cited 2020 Dec 01]. Available from: http://hdl.handle.net/2298/11144.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

谷脇, 琢也; タニワキ . 可変型遺伝子トラップベクターpU-17を用いたトラップラインの樹立と解析 : カヘンガタ イデンシ トラップ ベクター pU-17 オ モチイタ トラップ ライン ノ ジュリツ ト カイセキ; Characterization of an exchangeable gene trap using pU-17 carrying a stop codon-βgeo cassette. [Thesis]. Kumamoto University / 熊本大学; Available from: http://hdl.handle.net/2298/11144

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


Indian Institute of Science

19. Dhar, Debojyoti. Regulation Of Interferon Regulatory Factor-2 mRNA Translation By 'IRES' Element : Possible Role Of trans Acting Factors.

Degree: PhD, Faculty of Science, 2009, Indian Institute of Science

 Cellular response to various stress conditions involves regulation of gene expression by different mechanisms. Translation is the final step in the flow of genetic information… (more)

Subjects/Keywords: mRNA; Messenger RNA; Polypyrimidine; Interferon Rgulatory Factor-2 (IRF2); Internal Ribosome Entry Site (IRES); Polypyrimidine Tract Binding Protein; Gene Expression; trans Acting Factors; Biochemical Genetics

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APA (6th Edition):

Dhar, D. (2009). Regulation Of Interferon Regulatory Factor-2 mRNA Translation By 'IRES' Element : Possible Role Of trans Acting Factors. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/607

Chicago Manual of Style (16th Edition):

Dhar, Debojyoti. “Regulation Of Interferon Regulatory Factor-2 mRNA Translation By 'IRES' Element : Possible Role Of trans Acting Factors.” 2009. Doctoral Dissertation, Indian Institute of Science. Accessed December 01, 2020. http://etd.iisc.ac.in/handle/2005/607.

MLA Handbook (7th Edition):

Dhar, Debojyoti. “Regulation Of Interferon Regulatory Factor-2 mRNA Translation By 'IRES' Element : Possible Role Of trans Acting Factors.” 2009. Web. 01 Dec 2020.

Vancouver:

Dhar D. Regulation Of Interferon Regulatory Factor-2 mRNA Translation By 'IRES' Element : Possible Role Of trans Acting Factors. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2009. [cited 2020 Dec 01]. Available from: http://etd.iisc.ac.in/handle/2005/607.

Council of Science Editors:

Dhar D. Regulation Of Interferon Regulatory Factor-2 mRNA Translation By 'IRES' Element : Possible Role Of trans Acting Factors. [Doctoral Dissertation]. Indian Institute of Science; 2009. Available from: http://etd.iisc.ac.in/handle/2005/607

.