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You searched for subject:(RNA protein interactions). Showing records 1 – 30 of 124 total matches.

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Texas State University – San Marcos

1. Salas, Eliseo. Characterizing the ligand specificity of the RNA binding protein LARP6.

Degree: MS, Biochemistry, 2017, Texas State University – San Marcos

 The La-related proteins are a superfamily of RNA-binding proteins characterized by a unique RNA binding domain that is comprised of two subdomains, the La motif… (more)

Subjects/Keywords: LARP6; RNA; RNA-protein interactions

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APA (6th Edition):

Salas, E. (2017). Characterizing the ligand specificity of the RNA binding protein LARP6. (Masters Thesis). Texas State University – San Marcos. Retrieved from https://digital.library.txstate.edu/handle/10877/7733

Chicago Manual of Style (16th Edition):

Salas, Eliseo. “Characterizing the ligand specificity of the RNA binding protein LARP6.” 2017. Masters Thesis, Texas State University – San Marcos. Accessed November 30, 2020. https://digital.library.txstate.edu/handle/10877/7733.

MLA Handbook (7th Edition):

Salas, Eliseo. “Characterizing the ligand specificity of the RNA binding protein LARP6.” 2017. Web. 30 Nov 2020.

Vancouver:

Salas E. Characterizing the ligand specificity of the RNA binding protein LARP6. [Internet] [Masters thesis]. Texas State University – San Marcos; 2017. [cited 2020 Nov 30]. Available from: https://digital.library.txstate.edu/handle/10877/7733.

Council of Science Editors:

Salas E. Characterizing the ligand specificity of the RNA binding protein LARP6. [Masters Thesis]. Texas State University – San Marcos; 2017. Available from: https://digital.library.txstate.edu/handle/10877/7733


Hong Kong University of Science and Technology

2. Marini, Simone. Qualitative and quantitative protein interaction prediction with machine learning.

Degree: 2012, Hong Kong University of Science and Technology

Protein interactions constitute a crucial part of the cell metabolsim. In particular, protein-protein, DNA-protein and RNA-protein interactions play a critical role in the whole cellular… (more)

Subjects/Keywords: Protein-protein interactions ; DNA-protein interactions ; RNA-protein interactions ; Machine learning

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APA (6th Edition):

Marini, S. (2012). Qualitative and quantitative protein interaction prediction with machine learning. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-62600 ; https://doi.org/10.14711/thesis-b1198684 ; http://repository.ust.hk/ir/bitstream/1783.1-62600/1/th_redirect.html

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):

Marini, Simone. “Qualitative and quantitative protein interaction prediction with machine learning.” 2012. Thesis, Hong Kong University of Science and Technology. Accessed November 30, 2020. http://repository.ust.hk/ir/Record/1783.1-62600 ; https://doi.org/10.14711/thesis-b1198684 ; http://repository.ust.hk/ir/bitstream/1783.1-62600/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Marini, Simone. “Qualitative and quantitative protein interaction prediction with machine learning.” 2012. Web. 30 Nov 2020.

Vancouver:

Marini S. Qualitative and quantitative protein interaction prediction with machine learning. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2012. [cited 2020 Nov 30]. Available from: http://repository.ust.hk/ir/Record/1783.1-62600 ; https://doi.org/10.14711/thesis-b1198684 ; http://repository.ust.hk/ir/bitstream/1783.1-62600/1/th_redirect.html.

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

Council of Science Editors:

Marini S. Qualitative and quantitative protein interaction prediction with machine learning. [Thesis]. Hong Kong University of Science and Technology; 2012. Available from: http://repository.ust.hk/ir/Record/1783.1-62600 ; https://doi.org/10.14711/thesis-b1198684 ; http://repository.ust.hk/ir/bitstream/1783.1-62600/1/th_redirect.html

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


IUPUI

3. Alakhras, Nada S. A method to isolate the CTD of RNA Polymerase II for proteomics analysis.

Degree: 2014, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

In an effort to advance the methodology in analyzing RNAPII protein-protein interaction network and to determine the role of the… (more)

Subjects/Keywords: RNA polymerases; RNA-protein interactions; Protein-protein interactions; Retroviruses; Qualitative research

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APA (6th Edition):

Alakhras, N. S. (2014). A method to isolate the CTD of RNA Polymerase II for proteomics analysis. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/6179

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):

Alakhras, Nada S. “A method to isolate the CTD of RNA Polymerase II for proteomics analysis.” 2014. Thesis, IUPUI. Accessed November 30, 2020. http://hdl.handle.net/1805/6179.

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

MLA Handbook (7th Edition):

Alakhras, Nada S. “A method to isolate the CTD of RNA Polymerase II for proteomics analysis.” 2014. Web. 30 Nov 2020.

Vancouver:

Alakhras NS. A method to isolate the CTD of RNA Polymerase II for proteomics analysis. [Internet] [Thesis]. IUPUI; 2014. [cited 2020 Nov 30]. Available from: http://hdl.handle.net/1805/6179.

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

Council of Science Editors:

Alakhras NS. A method to isolate the CTD of RNA Polymerase II for proteomics analysis. [Thesis]. IUPUI; 2014. Available from: http://hdl.handle.net/1805/6179

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


York University

4. Vinayak, Jyotsna. Human La Function in Expression of Coding Transcripts.

Degree: PhD, Biology, 2018, York University

 The La protein, also referred to as Sjogrens Syndrome antigen B (SSB), is an RNA-binding phosphoprotein first identified as an auto-antigen in patients suffering from… (more)

Subjects/Keywords: Biochemistry; Molecular Biology; RNA; RNA-Protein Interactions

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APA (6th Edition):

Vinayak, J. (2018). Human La Function in Expression of Coding Transcripts. (Doctoral Dissertation). York University. Retrieved from http://hdl.handle.net/10315/35509

Chicago Manual of Style (16th Edition):

Vinayak, Jyotsna. “Human La Function in Expression of Coding Transcripts.” 2018. Doctoral Dissertation, York University. Accessed November 30, 2020. http://hdl.handle.net/10315/35509.

MLA Handbook (7th Edition):

Vinayak, Jyotsna. “Human La Function in Expression of Coding Transcripts.” 2018. Web. 30 Nov 2020.

Vancouver:

Vinayak J. Human La Function in Expression of Coding Transcripts. [Internet] [Doctoral dissertation]. York University; 2018. [cited 2020 Nov 30]. Available from: http://hdl.handle.net/10315/35509.

Council of Science Editors:

Vinayak J. Human La Function in Expression of Coding Transcripts. [Doctoral Dissertation]. York University; 2018. Available from: http://hdl.handle.net/10315/35509


Columbia University

5. Weyn-Vanhentenryck, Sabastien Matthieu. Regulation of splicing networks in neurodevelopment.

Degree: 2018, Columbia University

 Alternative splicing of pre-mRNA is a critical mechanism for enabling genetic diversity, and is a carefully regulated process in neuronal differentiation. RNA binding proteins (RBPs)… (more)

Subjects/Keywords: Bioinformatics; Neurosciences; RNA splicing; RNA-protein interactions

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APA (6th Edition):

Weyn-Vanhentenryck, S. M. (2018). Regulation of splicing networks in neurodevelopment. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8SR0BZF

Chicago Manual of Style (16th Edition):

Weyn-Vanhentenryck, Sabastien Matthieu. “Regulation of splicing networks in neurodevelopment.” 2018. Doctoral Dissertation, Columbia University. Accessed November 30, 2020. https://doi.org/10.7916/D8SR0BZF.

MLA Handbook (7th Edition):

Weyn-Vanhentenryck, Sabastien Matthieu. “Regulation of splicing networks in neurodevelopment.” 2018. Web. 30 Nov 2020.

Vancouver:

Weyn-Vanhentenryck SM. Regulation of splicing networks in neurodevelopment. [Internet] [Doctoral dissertation]. Columbia University; 2018. [cited 2020 Nov 30]. Available from: https://doi.org/10.7916/D8SR0BZF.

Council of Science Editors:

Weyn-Vanhentenryck SM. Regulation of splicing networks in neurodevelopment. [Doctoral Dissertation]. Columbia University; 2018. Available from: https://doi.org/10.7916/D8SR0BZF


Portland State University

6. Deutsch, Christopher Wayne. Discovery and Characterization of the Proteins Involved in the Synthesis of N⁶-Threonylcarbamoyl Adenosine, a Nucleoside Modification of tRNA.

Degree: PhD, Chemistry, 2016, Portland State University

  N6-threonylcarbamoyl adenosine (t6A) is a universally conserved tRNA modification found at position 37 of tRNAs which decode ANN codons. Structural studies have implicated its… (more)

Subjects/Keywords: Transfer RNA; Biosynthesis; RNA-protein interactions; Chemistry

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APA (6th Edition):

Deutsch, C. W. (2016). Discovery and Characterization of the Proteins Involved in the Synthesis of N⁶-Threonylcarbamoyl Adenosine, a Nucleoside Modification of tRNA. (Doctoral Dissertation). Portland State University. Retrieved from https://pdxscholar.library.pdx.edu/open_access_etds/3080

Chicago Manual of Style (16th Edition):

Deutsch, Christopher Wayne. “Discovery and Characterization of the Proteins Involved in the Synthesis of N⁶-Threonylcarbamoyl Adenosine, a Nucleoside Modification of tRNA.” 2016. Doctoral Dissertation, Portland State University. Accessed November 30, 2020. https://pdxscholar.library.pdx.edu/open_access_etds/3080.

MLA Handbook (7th Edition):

Deutsch, Christopher Wayne. “Discovery and Characterization of the Proteins Involved in the Synthesis of N⁶-Threonylcarbamoyl Adenosine, a Nucleoside Modification of tRNA.” 2016. Web. 30 Nov 2020.

Vancouver:

Deutsch CW. Discovery and Characterization of the Proteins Involved in the Synthesis of N⁶-Threonylcarbamoyl Adenosine, a Nucleoside Modification of tRNA. [Internet] [Doctoral dissertation]. Portland State University; 2016. [cited 2020 Nov 30]. Available from: https://pdxscholar.library.pdx.edu/open_access_etds/3080.

Council of Science Editors:

Deutsch CW. Discovery and Characterization of the Proteins Involved in the Synthesis of N⁶-Threonylcarbamoyl Adenosine, a Nucleoside Modification of tRNA. [Doctoral Dissertation]. Portland State University; 2016. Available from: https://pdxscholar.library.pdx.edu/open_access_etds/3080


Penn State University

7. Quan, Chao. Structural Studies of Yeast RNase MRP Complex .

Degree: 2011, Penn State University

 RNase MRP is a ubiquitous and essential eukaryotic enzyme. In budding yeast (S. cerevisiae), RNase MRP is involved in the biogenesis of ribosome and regulation… (more)

Subjects/Keywords: RNA-protein interactions; RPP1_POP5; RNase MRP; protein-protein interactions

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APA (6th Edition):

Quan, C. (2011). Structural Studies of Yeast RNase MRP Complex . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/11269

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):

Quan, Chao. “Structural Studies of Yeast RNase MRP Complex .” 2011. Thesis, Penn State University. Accessed November 30, 2020. https://submit-etda.libraries.psu.edu/catalog/11269.

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

MLA Handbook (7th Edition):

Quan, Chao. “Structural Studies of Yeast RNase MRP Complex .” 2011. Web. 30 Nov 2020.

Vancouver:

Quan C. Structural Studies of Yeast RNase MRP Complex . [Internet] [Thesis]. Penn State University; 2011. [cited 2020 Nov 30]. Available from: https://submit-etda.libraries.psu.edu/catalog/11269.

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

Council of Science Editors:

Quan C. Structural Studies of Yeast RNase MRP Complex . [Thesis]. Penn State University; 2011. Available from: https://submit-etda.libraries.psu.edu/catalog/11269

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


Indian Institute of Science

8. Swapna, L S. Structural And Evolutionary Studies On Protein-Protein Interactions.

Degree: PhD, Faculty of Science, 2014, Indian Institute of Science

 The last few decades have witnessed an upsurge in the availability of large-scale data on genomes and genome-scale information. The development of methods to understand… (more)

Subjects/Keywords: Protein-Protein Interactions; Protein-Protein Complexes; Protein-Protein Structure; Homodimeric Proteins; Transient Protein-Protein Complexes; Protein-Protein Interactions - Structure; Protein-Protein Interactions - Evolution; Protein-Protein Interfaces; RNA Polymerase; Biochemistry

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APA (6th Edition):

Swapna, L. S. (2014). Structural And Evolutionary Studies On Protein-Protein Interactions. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/2316

Chicago Manual of Style (16th Edition):

Swapna, L S. “Structural And Evolutionary Studies On Protein-Protein Interactions.” 2014. Doctoral Dissertation, Indian Institute of Science. Accessed November 30, 2020. http://etd.iisc.ac.in/handle/2005/2316.

MLA Handbook (7th Edition):

Swapna, L S. “Structural And Evolutionary Studies On Protein-Protein Interactions.” 2014. Web. 30 Nov 2020.

Vancouver:

Swapna LS. Structural And Evolutionary Studies On Protein-Protein Interactions. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2014. [cited 2020 Nov 30]. Available from: http://etd.iisc.ac.in/handle/2005/2316.

Council of Science Editors:

Swapna LS. Structural And Evolutionary Studies On Protein-Protein Interactions. [Doctoral Dissertation]. Indian Institute of Science; 2014. Available from: http://etd.iisc.ac.in/handle/2005/2316


Georgia Tech

9. Jung, Jeenah. Development of optical imaging method for detecting RNA-protein interactions.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2014, Georgia Tech

 The localization and translation of messenger ribonucleic acids (mRNAs) play crucial roles in cellular function and diseases, and are regulated by numerous RNA-binding proteins (RBPs)… (more)

Subjects/Keywords: RNA-protein interactions; Post-transcriptional regulation

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APA (6th Edition):

Jung, J. (2014). Development of optical imaging method for detecting RNA-protein interactions. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54278

Chicago Manual of Style (16th Edition):

Jung, Jeenah. “Development of optical imaging method for detecting RNA-protein interactions.” 2014. Doctoral Dissertation, Georgia Tech. Accessed November 30, 2020. http://hdl.handle.net/1853/54278.

MLA Handbook (7th Edition):

Jung, Jeenah. “Development of optical imaging method for detecting RNA-protein interactions.” 2014. Web. 30 Nov 2020.

Vancouver:

Jung J. Development of optical imaging method for detecting RNA-protein interactions. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2020 Nov 30]. Available from: http://hdl.handle.net/1853/54278.

Council of Science Editors:

Jung J. Development of optical imaging method for detecting RNA-protein interactions. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/54278


University of Kansas

10. Gowthaman, Ragul. Computational approaches to identify small-molecule inhibitors of non-traditional drug targets.

Degree: PhD, Molecular Biosciences, 2015, University of Kansas

 Non-traditional targets for therapeutic intervention are those proteins that have not evolved to bind small molecules, but have instead evolved to bind other macromolecules. Such… (more)

Subjects/Keywords: Bioinformatics; DARC; pharmacophore mimicry; Protein-protein interactions; Protein-RNA interactions; shape matching; virtual screening

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APA (6th Edition):

Gowthaman, R. (2015). Computational approaches to identify small-molecule inhibitors of non-traditional drug targets. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/23975

Chicago Manual of Style (16th Edition):

Gowthaman, Ragul. “Computational approaches to identify small-molecule inhibitors of non-traditional drug targets.” 2015. Doctoral Dissertation, University of Kansas. Accessed November 30, 2020. http://hdl.handle.net/1808/23975.

MLA Handbook (7th Edition):

Gowthaman, Ragul. “Computational approaches to identify small-molecule inhibitors of non-traditional drug targets.” 2015. Web. 30 Nov 2020.

Vancouver:

Gowthaman R. Computational approaches to identify small-molecule inhibitors of non-traditional drug targets. [Internet] [Doctoral dissertation]. University of Kansas; 2015. [cited 2020 Nov 30]. Available from: http://hdl.handle.net/1808/23975.

Council of Science Editors:

Gowthaman R. Computational approaches to identify small-molecule inhibitors of non-traditional drug targets. [Doctoral Dissertation]. University of Kansas; 2015. Available from: http://hdl.handle.net/1808/23975


Columbia University

11. Tan, Dazhi. Molecular Basis for the Recognition of the Regulatory Stem-loop Structures in Eukaryotic Messenger RNAs.

Degree: 2014, Columbia University

 Apart from carrying genetic information, RNAs also act as effectors of cellular processes through folding into intricate secondary and tertiary structures. The ubiquitous RNA structures… (more)

Subjects/Keywords: Messenger RNA; RNA-protein interactions; Eukaryotic cells; Biology; Biochemistry; Molecular biology

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APA (6th Edition):

Tan, D. (2014). Molecular Basis for the Recognition of the Regulatory Stem-loop Structures in Eukaryotic Messenger RNAs. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8FN14B4

Chicago Manual of Style (16th Edition):

Tan, Dazhi. “Molecular Basis for the Recognition of the Regulatory Stem-loop Structures in Eukaryotic Messenger RNAs.” 2014. Doctoral Dissertation, Columbia University. Accessed November 30, 2020. https://doi.org/10.7916/D8FN14B4.

MLA Handbook (7th Edition):

Tan, Dazhi. “Molecular Basis for the Recognition of the Regulatory Stem-loop Structures in Eukaryotic Messenger RNAs.” 2014. Web. 30 Nov 2020.

Vancouver:

Tan D. Molecular Basis for the Recognition of the Regulatory Stem-loop Structures in Eukaryotic Messenger RNAs. [Internet] [Doctoral dissertation]. Columbia University; 2014. [cited 2020 Nov 30]. Available from: https://doi.org/10.7916/D8FN14B4.

Council of Science Editors:

Tan D. Molecular Basis for the Recognition of the Regulatory Stem-loop Structures in Eukaryotic Messenger RNAs. [Doctoral Dissertation]. Columbia University; 2014. Available from: https://doi.org/10.7916/D8FN14B4


University of Hong Kong

12. 陳燕彤. Demonstration of specific physical interaction between CHOP mRNA and intracellular proteins.

Degree: 2011, University of Hong Kong

 The ability of a cell to respond precisely to environmental stress depends on the expression of a large number of genes in a finely coordinated… (more)

Subjects/Keywords: Messenger RNA.; RNA-protein interactions.

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APA (6th Edition):

陳燕彤.. (2011). Demonstration of specific physical interaction between CHOP mRNA and intracellular proteins. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/174332

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

Chicago Manual of Style (16th Edition):

陳燕彤.. “Demonstration of specific physical interaction between CHOP mRNA and intracellular proteins.” 2011. Thesis, University of Hong Kong. Accessed November 30, 2020. http://hdl.handle.net/10722/174332.

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

MLA Handbook (7th Edition):

陳燕彤.. “Demonstration of specific physical interaction between CHOP mRNA and intracellular proteins.” 2011. Web. 30 Nov 2020.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

陳燕彤.. Demonstration of specific physical interaction between CHOP mRNA and intracellular proteins. [Internet] [Thesis]. University of Hong Kong; 2011. [cited 2020 Nov 30]. Available from: http://hdl.handle.net/10722/174332.

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

Council of Science Editors:

陳燕彤.. Demonstration of specific physical interaction between CHOP mRNA and intracellular proteins. [Thesis]. University of Hong Kong; 2011. Available from: http://hdl.handle.net/10722/174332

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


University of Texas – Austin

13. Roth, Andrew Adam. Snu40p and Snu66p are required for spliceosome activation at suboptimal temperatures.

Degree: PhD, Cell and Molecular Biology, 2008, University of Texas – Austin

 In addressing the pre-mRNA substrate, the splicing machinery requires rearrangement of multiple RNA and protein components. The classical model of spliceosome formation begins with the… (more)

Subjects/Keywords: RNA splicing; RNA-protein interactions

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APA (6th Edition):

Roth, A. A. (2008). Snu40p and Snu66p are required for spliceosome activation at suboptimal temperatures. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/4005

Chicago Manual of Style (16th Edition):

Roth, Andrew Adam. “Snu40p and Snu66p are required for spliceosome activation at suboptimal temperatures.” 2008. Doctoral Dissertation, University of Texas – Austin. Accessed November 30, 2020. http://hdl.handle.net/2152/4005.

MLA Handbook (7th Edition):

Roth, Andrew Adam. “Snu40p and Snu66p are required for spliceosome activation at suboptimal temperatures.” 2008. Web. 30 Nov 2020.

Vancouver:

Roth AA. Snu40p and Snu66p are required for spliceosome activation at suboptimal temperatures. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2008. [cited 2020 Nov 30]. Available from: http://hdl.handle.net/2152/4005.

Council of Science Editors:

Roth AA. Snu40p and Snu66p are required for spliceosome activation at suboptimal temperatures. [Doctoral Dissertation]. University of Texas – Austin; 2008. Available from: http://hdl.handle.net/2152/4005


Bowling Green State University

14. Roy, Poorna, Roy. Analyzing and classifying bimolecular interactions:I. Effects of metal binding on an iron-sulfur cluster scaffold proteinII. Automatic annotation of RNA-protein interactions for NDB.

Degree: PhD, Photochemical Sciences, 2017, Bowling Green State University

 This dissertation comprises two distinct parts; however the different research agendas are thematically linked by their complementary approaches to investigate the nature of important intermolecular… (more)

Subjects/Keywords: Bioinformatics; Biochemistry; Iron-sulfur proteins; metalloprotein; RNA, RNA-protein interactions

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APA (6th Edition):

Roy, Poorna, R. (2017). Analyzing and classifying bimolecular interactions:I. Effects of metal binding on an iron-sulfur cluster scaffold proteinII. Automatic annotation of RNA-protein interactions for NDB. (Doctoral Dissertation). Bowling Green State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1496412736120654

Chicago Manual of Style (16th Edition):

Roy, Poorna, Roy. “Analyzing and classifying bimolecular interactions:I. Effects of metal binding on an iron-sulfur cluster scaffold proteinII. Automatic annotation of RNA-protein interactions for NDB.” 2017. Doctoral Dissertation, Bowling Green State University. Accessed November 30, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1496412736120654.

MLA Handbook (7th Edition):

Roy, Poorna, Roy. “Analyzing and classifying bimolecular interactions:I. Effects of metal binding on an iron-sulfur cluster scaffold proteinII. Automatic annotation of RNA-protein interactions for NDB.” 2017. Web. 30 Nov 2020.

Vancouver:

Roy, Poorna R. Analyzing and classifying bimolecular interactions:I. Effects of metal binding on an iron-sulfur cluster scaffold proteinII. Automatic annotation of RNA-protein interactions for NDB. [Internet] [Doctoral dissertation]. Bowling Green State University; 2017. [cited 2020 Nov 30]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1496412736120654.

Council of Science Editors:

Roy, Poorna R. Analyzing and classifying bimolecular interactions:I. Effects of metal binding on an iron-sulfur cluster scaffold proteinII. Automatic annotation of RNA-protein interactions for NDB. [Doctoral Dissertation]. Bowling Green State University; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1496412736120654


University of California – Santa Cruz

15. Howard, Jonathan Michael. Investigation Of In Vivo RNA-Protein Interactions Using Individual Nucleotide Resolution Cross-Linking Immunoprecipitation (ICLIP).

Degree: Molecular Cell and Developmental Biology, 2015, University of California – Santa Cruz

 Eukaryotic gene expression involves a complex system of checkpoints that regulate RNA biogenesis, maturation, and localization. Along the way, these RNA will encounter a host… (more)

Subjects/Keywords: Molecular biology; iCLIP; Pre-mRNA splicing; RNA binding proteins; RNA Biology; RNA-Protein interactions; Transcriptomics

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APA (6th Edition):

Howard, J. M. (2015). Investigation Of In Vivo RNA-Protein Interactions Using Individual Nucleotide Resolution Cross-Linking Immunoprecipitation (ICLIP). (Thesis). University of California – Santa Cruz. Retrieved from http://www.escholarship.org/uc/item/1483v1tz

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):

Howard, Jonathan Michael. “Investigation Of In Vivo RNA-Protein Interactions Using Individual Nucleotide Resolution Cross-Linking Immunoprecipitation (ICLIP).” 2015. Thesis, University of California – Santa Cruz. Accessed November 30, 2020. http://www.escholarship.org/uc/item/1483v1tz.

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

MLA Handbook (7th Edition):

Howard, Jonathan Michael. “Investigation Of In Vivo RNA-Protein Interactions Using Individual Nucleotide Resolution Cross-Linking Immunoprecipitation (ICLIP).” 2015. Web. 30 Nov 2020.

Vancouver:

Howard JM. Investigation Of In Vivo RNA-Protein Interactions Using Individual Nucleotide Resolution Cross-Linking Immunoprecipitation (ICLIP). [Internet] [Thesis]. University of California – Santa Cruz; 2015. [cited 2020 Nov 30]. Available from: http://www.escholarship.org/uc/item/1483v1tz.

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

Council of Science Editors:

Howard JM. Investigation Of In Vivo RNA-Protein Interactions Using Individual Nucleotide Resolution Cross-Linking Immunoprecipitation (ICLIP). [Thesis]. University of California – Santa Cruz; 2015. Available from: http://www.escholarship.org/uc/item/1483v1tz

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


University of Newcastle

16. Harriott, Kate. The characterisation of the interaction between PcrA and RNA polymerase.

Degree: PhD, 2012, University of Newcastle

Research Doctorate - Doctor of Philosophy (PhD)

RNA polymerase (RNAP) is the highly conserved multi-subunit enzyme that carries out transcription in all life forms. RNAP… (more)

Subjects/Keywords: RNA polymerase; transcription; protein-protein interactions; PcrA; RNAP

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APA (6th Edition):

Harriott, K. (2012). The characterisation of the interaction between PcrA and RNA polymerase. (Doctoral Dissertation). University of Newcastle. Retrieved from http://hdl.handle.net/1959.13/932055

Chicago Manual of Style (16th Edition):

Harriott, Kate. “The characterisation of the interaction between PcrA and RNA polymerase.” 2012. Doctoral Dissertation, University of Newcastle. Accessed November 30, 2020. http://hdl.handle.net/1959.13/932055.

MLA Handbook (7th Edition):

Harriott, Kate. “The characterisation of the interaction between PcrA and RNA polymerase.” 2012. Web. 30 Nov 2020.

Vancouver:

Harriott K. The characterisation of the interaction between PcrA and RNA polymerase. [Internet] [Doctoral dissertation]. University of Newcastle; 2012. [cited 2020 Nov 30]. Available from: http://hdl.handle.net/1959.13/932055.

Council of Science Editors:

Harriott K. The characterisation of the interaction between PcrA and RNA polymerase. [Doctoral Dissertation]. University of Newcastle; 2012. Available from: http://hdl.handle.net/1959.13/932055


Macquarie University

17. Manea, Francesca. Engineering synthetic Lsm rings for applications in nanotechnology.

Degree: 2015, Macquarie University

Empirical thesis.

Bibliography: pages 201-220.

Protein-based tectons for nanobiotechnology  – Materials & methods  – Preparation & solution  – Quaternary structure assessment of Lsm tecton architectures… (more)

Subjects/Keywords: RNA-protein interactions; Nucleoproteins; Nanostructures; protein; engineering; nanotechnology

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APA (6th Edition):

Manea, F. (2015). Engineering synthetic Lsm rings for applications in nanotechnology. (Doctoral Dissertation). Macquarie University. Retrieved from http://hdl.handle.net/1959.14/1075221

Chicago Manual of Style (16th Edition):

Manea, Francesca. “Engineering synthetic Lsm rings for applications in nanotechnology.” 2015. Doctoral Dissertation, Macquarie University. Accessed November 30, 2020. http://hdl.handle.net/1959.14/1075221.

MLA Handbook (7th Edition):

Manea, Francesca. “Engineering synthetic Lsm rings for applications in nanotechnology.” 2015. Web. 30 Nov 2020.

Vancouver:

Manea F. Engineering synthetic Lsm rings for applications in nanotechnology. [Internet] [Doctoral dissertation]. Macquarie University; 2015. [cited 2020 Nov 30]. Available from: http://hdl.handle.net/1959.14/1075221.

Council of Science Editors:

Manea F. Engineering synthetic Lsm rings for applications in nanotechnology. [Doctoral Dissertation]. Macquarie University; 2015. Available from: http://hdl.handle.net/1959.14/1075221


Wayne State University

18. Lamichhane, Rajan. Study Of Protein-Rna Interactions Using Fluorescence Resonance Energy Transfer (fret) And Single-Molecule Fret.

Degree: PhD, Chemistry, 2011, Wayne State University

  In the cell, RNA and protein, interact to form ribonucleoprotein complexes (RNPs) that have vital structural, catalytic and regulatory roles. Despite their functional importance,… (more)

Subjects/Keywords: FRET; Non-coding RNA; Protein-RNA interactions; Ribosome; Single-molecule FRET; Splicing; Biochemistry; Chemistry

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APA (6th Edition):

Lamichhane, R. (2011). Study Of Protein-Rna Interactions Using Fluorescence Resonance Energy Transfer (fret) And Single-Molecule Fret. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/197

Chicago Manual of Style (16th Edition):

Lamichhane, Rajan. “Study Of Protein-Rna Interactions Using Fluorescence Resonance Energy Transfer (fret) And Single-Molecule Fret.” 2011. Doctoral Dissertation, Wayne State University. Accessed November 30, 2020. https://digitalcommons.wayne.edu/oa_dissertations/197.

MLA Handbook (7th Edition):

Lamichhane, Rajan. “Study Of Protein-Rna Interactions Using Fluorescence Resonance Energy Transfer (fret) And Single-Molecule Fret.” 2011. Web. 30 Nov 2020.

Vancouver:

Lamichhane R. Study Of Protein-Rna Interactions Using Fluorescence Resonance Energy Transfer (fret) And Single-Molecule Fret. [Internet] [Doctoral dissertation]. Wayne State University; 2011. [cited 2020 Nov 30]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/197.

Council of Science Editors:

Lamichhane R. Study Of Protein-Rna Interactions Using Fluorescence Resonance Energy Transfer (fret) And Single-Molecule Fret. [Doctoral Dissertation]. Wayne State University; 2011. Available from: https://digitalcommons.wayne.edu/oa_dissertations/197


Iowa State University

19. Ottesen, Eric William. Novel Functions of the Survival Motor Neuron Protein.

Degree: 2016, Iowa State University

 The Survival Motor Neuron (SMN) protein is a multi-functional protein that participates in a wide variety of critical pathways. Low levels of SMN cause spinal… (more)

Subjects/Keywords: HITS-CLIP; Protein-RNA interactions; RNA; SMN; Spinal Muscular Atrophy; Splicing; Molecular Biology

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APA (6th Edition):

Ottesen, E. W. (2016). Novel Functions of the Survival Motor Neuron Protein. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/15784

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):

Ottesen, Eric William. “Novel Functions of the Survival Motor Neuron Protein.” 2016. Thesis, Iowa State University. Accessed November 30, 2020. https://lib.dr.iastate.edu/etd/15784.

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

MLA Handbook (7th Edition):

Ottesen, Eric William. “Novel Functions of the Survival Motor Neuron Protein.” 2016. Web. 30 Nov 2020.

Vancouver:

Ottesen EW. Novel Functions of the Survival Motor Neuron Protein. [Internet] [Thesis]. Iowa State University; 2016. [cited 2020 Nov 30]. Available from: https://lib.dr.iastate.edu/etd/15784.

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

Council of Science Editors:

Ottesen EW. Novel Functions of the Survival Motor Neuron Protein. [Thesis]. Iowa State University; 2016. Available from: https://lib.dr.iastate.edu/etd/15784

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


Macquarie University

20. Moll, Jens Mark. Structural characterisation of yeast Lsm protein complexes.

Degree: PhD, 2011, Macquarie University

Bibliography: p. 179-195.

Introduction  – Materials and methods  – Solution behaviour of Lsm polyproteins  – Biophysical characterisation of Lsm complexes and their RNA interactions  –… (more)

Subjects/Keywords: RNA-protein interactions; Nucleoproteins; Recombinant proteins; Protein-protein interactions; Complex compounds; Lsm; Sm like; mRNA degradation; macromolecular complexes

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Moll, J. M. (2011). Structural characterisation of yeast Lsm protein complexes. (Doctoral Dissertation). Macquarie University. Retrieved from http://hdl.handle.net/1959.14/192059

Chicago Manual of Style (16th Edition):

Moll, Jens Mark. “Structural characterisation of yeast Lsm protein complexes.” 2011. Doctoral Dissertation, Macquarie University. Accessed November 30, 2020. http://hdl.handle.net/1959.14/192059.

MLA Handbook (7th Edition):

Moll, Jens Mark. “Structural characterisation of yeast Lsm protein complexes.” 2011. Web. 30 Nov 2020.

Vancouver:

Moll JM. Structural characterisation of yeast Lsm protein complexes. [Internet] [Doctoral dissertation]. Macquarie University; 2011. [cited 2020 Nov 30]. Available from: http://hdl.handle.net/1959.14/192059.

Council of Science Editors:

Moll JM. Structural characterisation of yeast Lsm protein complexes. [Doctoral Dissertation]. Macquarie University; 2011. Available from: http://hdl.handle.net/1959.14/192059

21. Angius, Federica. Molecular basis of membrane protein production and intracellular membranes proliferation in E. coli : Base moléculaire de la production des protéines membranaires et de la formation des membranes intracellulaire dans Escherichia coli.

Degree: Docteur es, Physiologie et biologie des organismes, populations, interactions. Biologie moléculaire, 2017, Sorbonne Paris Cité

Le système d’expression le plus utilisé pour la production des protéines membranaires, est le système basé sur l’ARN polymérase T7 (ARNpol T7) (Hattab et al.,… (more)

Subjects/Keywords: ARN T7 polymérase; Interactions protéine-lipide; T7 RNA polymerase; Protein-lipid interactions

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APA (6th Edition):

Angius, F. (2017). Molecular basis of membrane protein production and intracellular membranes proliferation in E. coli : Base moléculaire de la production des protéines membranaires et de la formation des membranes intracellulaire dans Escherichia coli. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2017USPCC217

Chicago Manual of Style (16th Edition):

Angius, Federica. “Molecular basis of membrane protein production and intracellular membranes proliferation in E. coli : Base moléculaire de la production des protéines membranaires et de la formation des membranes intracellulaire dans Escherichia coli.” 2017. Doctoral Dissertation, Sorbonne Paris Cité. Accessed November 30, 2020. http://www.theses.fr/2017USPCC217.

MLA Handbook (7th Edition):

Angius, Federica. “Molecular basis of membrane protein production and intracellular membranes proliferation in E. coli : Base moléculaire de la production des protéines membranaires et de la formation des membranes intracellulaire dans Escherichia coli.” 2017. Web. 30 Nov 2020.

Vancouver:

Angius F. Molecular basis of membrane protein production and intracellular membranes proliferation in E. coli : Base moléculaire de la production des protéines membranaires et de la formation des membranes intracellulaire dans Escherichia coli. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2017. [cited 2020 Nov 30]. Available from: http://www.theses.fr/2017USPCC217.

Council of Science Editors:

Angius F. Molecular basis of membrane protein production and intracellular membranes proliferation in E. coli : Base moléculaire de la production des protéines membranaires et de la formation des membranes intracellulaire dans Escherichia coli. [Doctoral Dissertation]. Sorbonne Paris Cité; 2017. Available from: http://www.theses.fr/2017USPCC217


Rhodes University

22. Burger, Adélle. The E.coli RNA degradosome analysis of molecular chaperones and enolase.

Degree: MS, Faculty of Science, Biochemistry, Microbiology and Biotechnology, 2010, Rhodes University

 Normal mRNA turnover is essential for genetic regulation within cells. The E. coli RNA degradosome, a large multi-component protein complex which originates through specific protein(more)

Subjects/Keywords: Molecular chaperones; Escherichia coli  – Biotechnology; Polyphosphates; Polyphosphates  – Biotechnology; RNA-protein interactions

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APA (6th Edition):

Burger, A. (2010). The E.coli RNA degradosome analysis of molecular chaperones and enolase. (Masters Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1004009

Chicago Manual of Style (16th Edition):

Burger, Adélle. “The E.coli RNA degradosome analysis of molecular chaperones and enolase.” 2010. Masters Thesis, Rhodes University. Accessed November 30, 2020. http://hdl.handle.net/10962/d1004009.

MLA Handbook (7th Edition):

Burger, Adélle. “The E.coli RNA degradosome analysis of molecular chaperones and enolase.” 2010. Web. 30 Nov 2020.

Vancouver:

Burger A. The E.coli RNA degradosome analysis of molecular chaperones and enolase. [Internet] [Masters thesis]. Rhodes University; 2010. [cited 2020 Nov 30]. Available from: http://hdl.handle.net/10962/d1004009.

Council of Science Editors:

Burger A. The E.coli RNA degradosome analysis of molecular chaperones and enolase. [Masters Thesis]. Rhodes University; 2010. Available from: http://hdl.handle.net/10962/d1004009


Texas A&M University

23. Ramesh, Arati. Structural studies of the Ro ribonucleoprotein and the metalloregulator CsoR.

Degree: PhD, Biochemistry, 2009, Texas A&M University

 Ro ribonucleoproteins are antigenic protein-RNA particles that are the major targets of the immune reaction in autoimmune disorders like systemic lupus erythematosus. The Ro protein(more)

Subjects/Keywords: protein-RNA interactions; transcriptional regulators

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APA (6th Edition):

Ramesh, A. (2009). Structural studies of the Ro ribonucleoprotein and the metalloregulator CsoR. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-1426

Chicago Manual of Style (16th Edition):

Ramesh, Arati. “Structural studies of the Ro ribonucleoprotein and the metalloregulator CsoR.” 2009. Doctoral Dissertation, Texas A&M University. Accessed November 30, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-1426.

MLA Handbook (7th Edition):

Ramesh, Arati. “Structural studies of the Ro ribonucleoprotein and the metalloregulator CsoR.” 2009. Web. 30 Nov 2020.

Vancouver:

Ramesh A. Structural studies of the Ro ribonucleoprotein and the metalloregulator CsoR. [Internet] [Doctoral dissertation]. Texas A&M University; 2009. [cited 2020 Nov 30]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1426.

Council of Science Editors:

Ramesh A. Structural studies of the Ro ribonucleoprotein and the metalloregulator CsoR. [Doctoral Dissertation]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1426


University of Hong Kong

24. 呂柏賢. Role of double-stranded RNA-binding protein PACT in MDA5-mediated antiviral innate immune response.

Degree: 2014, University of Hong Kong

Subjects/Keywords: RNA-protein interactions; Immune response

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APA (6th Edition):

呂柏賢. (2014). Role of double-stranded RNA-binding protein PACT in MDA5-mediated antiviral innate immune response. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/208552

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

Chicago Manual of Style (16th Edition):

呂柏賢. “Role of double-stranded RNA-binding protein PACT in MDA5-mediated antiviral innate immune response.” 2014. Thesis, University of Hong Kong. Accessed November 30, 2020. http://hdl.handle.net/10722/208552.

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

MLA Handbook (7th Edition):

呂柏賢. “Role of double-stranded RNA-binding protein PACT in MDA5-mediated antiviral innate immune response.” 2014. Web. 30 Nov 2020.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

呂柏賢. Role of double-stranded RNA-binding protein PACT in MDA5-mediated antiviral innate immune response. [Internet] [Thesis]. University of Hong Kong; 2014. [cited 2020 Nov 30]. Available from: http://hdl.handle.net/10722/208552.

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

Council of Science Editors:

呂柏賢. Role of double-stranded RNA-binding protein PACT in MDA5-mediated antiviral innate immune response. [Thesis]. University of Hong Kong; 2014. Available from: http://hdl.handle.net/10722/208552

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


University of Hong Kong

25. Lui, Pak-yin. Role of double-stranded RNA-binding protein PACT in MDA5-mediated antiviral innate immune response.

Degree: 2014, University of Hong Kong

 Immunity is an evolutionary conserved ability to protect organisms from infection by pathogens that co-exist in the same ecosystem. In mammals, the immune system is… (more)

Subjects/Keywords: Immune response; RNA-protein interactions

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APA (6th Edition):

Lui, P. (2014). Role of double-stranded RNA-binding protein PACT in MDA5-mediated antiviral innate immune response. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/222199

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):

Lui, Pak-yin. “Role of double-stranded RNA-binding protein PACT in MDA5-mediated antiviral innate immune response.” 2014. Thesis, University of Hong Kong. Accessed November 30, 2020. http://hdl.handle.net/10722/222199.

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

MLA Handbook (7th Edition):

Lui, Pak-yin. “Role of double-stranded RNA-binding protein PACT in MDA5-mediated antiviral innate immune response.” 2014. Web. 30 Nov 2020.

Vancouver:

Lui P. Role of double-stranded RNA-binding protein PACT in MDA5-mediated antiviral innate immune response. [Internet] [Thesis]. University of Hong Kong; 2014. [cited 2020 Nov 30]. Available from: http://hdl.handle.net/10722/222199.

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

Council of Science Editors:

Lui P. Role of double-stranded RNA-binding protein PACT in MDA5-mediated antiviral innate immune response. [Thesis]. University of Hong Kong; 2014. Available from: http://hdl.handle.net/10722/222199

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


Massey University

26. Leung, Susanna Chui-Shan. Functional analysis of plant Mei2-like proteins.

Degree: MS, Biochemistry, 2003, Massey University

 Molecular techniques were used to analyse the function of a novel class of RNA-bindmg proteins in plants, termed Mei2-like. The biochemical function of this class… (more)

Subjects/Keywords: RNA-protein interactions; Genetic regulation

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APA (6th Edition):

Leung, S. C. (2003). Functional analysis of plant Mei2-like proteins. (Masters Thesis). Massey University. Retrieved from http://hdl.handle.net/10179/12632

Chicago Manual of Style (16th Edition):

Leung, Susanna Chui-Shan. “Functional analysis of plant Mei2-like proteins.” 2003. Masters Thesis, Massey University. Accessed November 30, 2020. http://hdl.handle.net/10179/12632.

MLA Handbook (7th Edition):

Leung, Susanna Chui-Shan. “Functional analysis of plant Mei2-like proteins.” 2003. Web. 30 Nov 2020.

Vancouver:

Leung SC. Functional analysis of plant Mei2-like proteins. [Internet] [Masters thesis]. Massey University; 2003. [cited 2020 Nov 30]. Available from: http://hdl.handle.net/10179/12632.

Council of Science Editors:

Leung SC. Functional analysis of plant Mei2-like proteins. [Masters Thesis]. Massey University; 2003. Available from: http://hdl.handle.net/10179/12632


Montana Tech

27. Havranek, Katherine Elizabeth. ANALYSIS OF RIFT VALLEY FEVER VIRUS HOST-PATHOGEN DYNAMICS.

Degree: PhD, 2019, Montana Tech

  Rift Valley fever virus (RVFV) is an emerging pathogen that causes severe disease in humans and domestic livestock. There is no licensed treatment or… (more)

Subjects/Keywords: nucleocapsid; protein-RNA interactions; Rift Valley fever virus; RIOK3; splicing; transcriptome

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APA (6th Edition):

Havranek, K. E. (2019). ANALYSIS OF RIFT VALLEY FEVER VIRUS HOST-PATHOGEN DYNAMICS. (Doctoral Dissertation). Montana Tech. Retrieved from https://scholarworks.umt.edu/etd/11372

Chicago Manual of Style (16th Edition):

Havranek, Katherine Elizabeth. “ANALYSIS OF RIFT VALLEY FEVER VIRUS HOST-PATHOGEN DYNAMICS.” 2019. Doctoral Dissertation, Montana Tech. Accessed November 30, 2020. https://scholarworks.umt.edu/etd/11372.

MLA Handbook (7th Edition):

Havranek, Katherine Elizabeth. “ANALYSIS OF RIFT VALLEY FEVER VIRUS HOST-PATHOGEN DYNAMICS.” 2019. Web. 30 Nov 2020.

Vancouver:

Havranek KE. ANALYSIS OF RIFT VALLEY FEVER VIRUS HOST-PATHOGEN DYNAMICS. [Internet] [Doctoral dissertation]. Montana Tech; 2019. [cited 2020 Nov 30]. Available from: https://scholarworks.umt.edu/etd/11372.

Council of Science Editors:

Havranek KE. ANALYSIS OF RIFT VALLEY FEVER VIRUS HOST-PATHOGEN DYNAMICS. [Doctoral Dissertation]. Montana Tech; 2019. Available from: https://scholarworks.umt.edu/etd/11372


Rutgers University

28. DeBoer, Erik Michael, 1980-. The role of HuD, a post-transcriptional regulator, in the development and function of the murine neocortex.

Degree: Neuroscience, 2014, Rutgers University

Subjects/Keywords: Neocortex; RNA-protein interactions

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APA (6th Edition):

DeBoer, Erik Michael, 1. (2014). The role of HuD, a post-transcriptional regulator, in the development and function of the murine neocortex. (Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/42374/

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):

DeBoer, Erik Michael, 1980-. “The role of HuD, a post-transcriptional regulator, in the development and function of the murine neocortex.” 2014. Thesis, Rutgers University. Accessed November 30, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/42374/.

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

MLA Handbook (7th Edition):

DeBoer, Erik Michael, 1980-. “The role of HuD, a post-transcriptional regulator, in the development and function of the murine neocortex.” 2014. Web. 30 Nov 2020.

Vancouver:

DeBoer, Erik Michael 1. The role of HuD, a post-transcriptional regulator, in the development and function of the murine neocortex. [Internet] [Thesis]. Rutgers University; 2014. [cited 2020 Nov 30]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/42374/.

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

Council of Science Editors:

DeBoer, Erik Michael 1. The role of HuD, a post-transcriptional regulator, in the development and function of the murine neocortex. [Thesis]. Rutgers University; 2014. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/42374/

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


University of Texas – Austin

29. SanFilippo, Joseph. The DNA-binding and DNA endonuclease domains of a group II intron-encoded protein: characterization and application to the engineering of gene-targeting vectors.

Degree: PhD, Cell and Molecular Biology, 2003, University of Texas – Austin

Subjects/Keywords: Introns; RNA-protein interactions; DNA

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APA (6th Edition):

SanFilippo, J. (2003). The DNA-binding and DNA endonuclease domains of a group II intron-encoded protein: characterization and application to the engineering of gene-targeting vectors. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/910

Chicago Manual of Style (16th Edition):

SanFilippo, Joseph. “The DNA-binding and DNA endonuclease domains of a group II intron-encoded protein: characterization and application to the engineering of gene-targeting vectors.” 2003. Doctoral Dissertation, University of Texas – Austin. Accessed November 30, 2020. http://hdl.handle.net/2152/910.

MLA Handbook (7th Edition):

SanFilippo, Joseph. “The DNA-binding and DNA endonuclease domains of a group II intron-encoded protein: characterization and application to the engineering of gene-targeting vectors.” 2003. Web. 30 Nov 2020.

Vancouver:

SanFilippo J. The DNA-binding and DNA endonuclease domains of a group II intron-encoded protein: characterization and application to the engineering of gene-targeting vectors. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2003. [cited 2020 Nov 30]. Available from: http://hdl.handle.net/2152/910.

Council of Science Editors:

SanFilippo J. The DNA-binding and DNA endonuclease domains of a group II intron-encoded protein: characterization and application to the engineering of gene-targeting vectors. [Doctoral Dissertation]. University of Texas – Austin; 2003. Available from: http://hdl.handle.net/2152/910


Rutgers University

30. Woltz, Ryan, 1986-. Hybrid structural biology studies reveal a novel mechanism by which influenza B NS1 protein suppresses host innate immune response.

Degree: PhD, Influenza  – Research, 2019, Rutgers University

Influenza is a highly contagious respiratory disease, which can have severe impacts on human health. Influenza type B is traditionally known as the seasonal flu… (more)

Subjects/Keywords: Chemistry and Chemical Biology; RNA-protein interactions; Immune response

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APA (6th Edition):

Woltz, Ryan, 1. (2019). Hybrid structural biology studies reveal a novel mechanism by which influenza B NS1 protein suppresses host innate immune response. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/61030/

Chicago Manual of Style (16th Edition):

Woltz, Ryan, 1986-. “Hybrid structural biology studies reveal a novel mechanism by which influenza B NS1 protein suppresses host innate immune response.” 2019. Doctoral Dissertation, Rutgers University. Accessed November 30, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/61030/.

MLA Handbook (7th Edition):

Woltz, Ryan, 1986-. “Hybrid structural biology studies reveal a novel mechanism by which influenza B NS1 protein suppresses host innate immune response.” 2019. Web. 30 Nov 2020.

Vancouver:

Woltz, Ryan 1. Hybrid structural biology studies reveal a novel mechanism by which influenza B NS1 protein suppresses host innate immune response. [Internet] [Doctoral dissertation]. Rutgers University; 2019. [cited 2020 Nov 30]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/61030/.

Council of Science Editors:

Woltz, Ryan 1. Hybrid structural biology studies reveal a novel mechanism by which influenza B NS1 protein suppresses host innate immune response. [Doctoral Dissertation]. Rutgers University; 2019. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/61030/

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