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You searched for +publisher:"University of Texas – Austin" +contributor:("Russell, Rick"). Showing records 1 – 30 of 46 total matches.

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University of Texas – Austin

1. -1411-8686. Exploring intron mobilization and detection of an intron gain event via intron transposition using a novel intron gain and loss reporter.

Degree: PhD, Cell and Molecular Biology, 2015, University of Texas – Austin

 Eukaryotic nuclear genes are discontinuous with the presence of intervening sequences termed spliceosomal introns. Once the DNA coding sequences are transcribed into pre-mRNA, these spliceosomal… (more)

Subjects/Keywords: Pre-mRNA splicing; Intron gain and loss; RPL8B; Intron transposition; Reverse splicing

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APA (6th Edition):

-1411-8686. (2015). Exploring intron mobilization and detection of an intron gain event via intron transposition using a novel intron gain and loss reporter. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46904

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

Chicago Manual of Style (16th Edition):

-1411-8686. “Exploring intron mobilization and detection of an intron gain event via intron transposition using a novel intron gain and loss reporter.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/46904.

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

MLA Handbook (7th Edition):

-1411-8686. “Exploring intron mobilization and detection of an intron gain event via intron transposition using a novel intron gain and loss reporter.” 2015. Web. 29 Oct 2020.

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

Vancouver:

-1411-8686. Exploring intron mobilization and detection of an intron gain event via intron transposition using a novel intron gain and loss reporter. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/46904.

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

Council of Science Editors:

-1411-8686. Exploring intron mobilization and detection of an intron gain event via intron transposition using a novel intron gain and loss reporter. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46904

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


University of Texas – Austin

2. Wu, Meilan. DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1.

Degree: PhD, Pharmaceutical Sciences, 2014, University of Texas – Austin

 Human PARP-1 is a nuclear protein containing six functional domains that catalyzes the poly(ADP-ribosyl)ation of a variety of protein substrates including itself. This process involves… (more)

Subjects/Keywords: Poly(ADP-ribosyl)ation; PARP-1

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APA (6th Edition):

Wu, M. (2014). DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/62238

Chicago Manual of Style (16th Edition):

Wu, Meilan. “DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/62238.

MLA Handbook (7th Edition):

Wu, Meilan. “DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1.” 2014. Web. 29 Oct 2020.

Vancouver:

Wu M. DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/62238.

Council of Science Editors:

Wu M. DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/62238


University of Texas – Austin

3. Wolf, Rachel Zepeda. Nuclear-encoded splicing factors for yeast mitochondrial introns.

Degree: PhD, Cell and molecular biology, 2015, University of Texas – Austin

 Hypothesized to be ancestors of eukaryotic spliceosomal introns, extant group II introns are found in bacteria, archaea, and in the mitochondria and chloroplast genomes of… (more)

Subjects/Keywords: Group II intron splicing; aI5gamma; bI1; Yeast mitochondrial introns

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APA (6th Edition):

Wolf, R. Z. (2015). Nuclear-encoded splicing factors for yeast mitochondrial introns. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/32223

Chicago Manual of Style (16th Edition):

Wolf, Rachel Zepeda. “Nuclear-encoded splicing factors for yeast mitochondrial introns.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/32223.

MLA Handbook (7th Edition):

Wolf, Rachel Zepeda. “Nuclear-encoded splicing factors for yeast mitochondrial introns.” 2015. Web. 29 Oct 2020.

Vancouver:

Wolf RZ. Nuclear-encoded splicing factors for yeast mitochondrial introns. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/32223.

Council of Science Editors:

Wolf RZ. Nuclear-encoded splicing factors for yeast mitochondrial introns. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/32223


University of Texas – Austin

4. Aguilar, Apolonio. The synthesis and anion binding studies of scorpiand-type calix[5]- and calix[10]phyrins as well as a cryptand-like bicyclic calix[15]phyrin system.

Degree: PhD, Chemistry, 2016, University of Texas – Austin

 The field of anion recognition in supramolecular chemistry has grown significantly in the past decade. The design challenges that are faced in targeting and sensing… (more)

Subjects/Keywords: Anion binding; Calixphyrins; Cryptands

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APA (6th Edition):

Aguilar, A. (2016). The synthesis and anion binding studies of scorpiand-type calix[5]- and calix[10]phyrins as well as a cryptand-like bicyclic calix[15]phyrin system. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/72827

Chicago Manual of Style (16th Edition):

Aguilar, Apolonio. “The synthesis and anion binding studies of scorpiand-type calix[5]- and calix[10]phyrins as well as a cryptand-like bicyclic calix[15]phyrin system.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/72827.

MLA Handbook (7th Edition):

Aguilar, Apolonio. “The synthesis and anion binding studies of scorpiand-type calix[5]- and calix[10]phyrins as well as a cryptand-like bicyclic calix[15]phyrin system.” 2016. Web. 29 Oct 2020.

Vancouver:

Aguilar A. The synthesis and anion binding studies of scorpiand-type calix[5]- and calix[10]phyrins as well as a cryptand-like bicyclic calix[15]phyrin system. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/72827.

Council of Science Editors:

Aguilar A. The synthesis and anion binding studies of scorpiand-type calix[5]- and calix[10]phyrins as well as a cryptand-like bicyclic calix[15]phyrin system. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/72827


University of Texas – Austin

5. Milligan, John N., Jr. Engineering isothermal amplification solutions for improved point of care diagnostics.

Degree: PhD, Cell and Molecular Biology, 2016, University of Texas – Austin

 Since their inception nearly 60 years ago, molecular diagnostics have amassed impressive achievements with respect to sensitivity, specificity, cost, complexity, and time to-result. Consequently, researchers… (more)

Subjects/Keywords: Point of care diagnostics; Isothermal amplification; DNA circuitry; Protein evolution

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APA (6th Edition):

Milligan, John N., J. (2016). Engineering isothermal amplification solutions for improved point of care diagnostics. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/72553

Chicago Manual of Style (16th Edition):

Milligan, John N., Jr. “Engineering isothermal amplification solutions for improved point of care diagnostics.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/72553.

MLA Handbook (7th Edition):

Milligan, John N., Jr. “Engineering isothermal amplification solutions for improved point of care diagnostics.” 2016. Web. 29 Oct 2020.

Vancouver:

Milligan, John N. J. Engineering isothermal amplification solutions for improved point of care diagnostics. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/72553.

Council of Science Editors:

Milligan, John N. J. Engineering isothermal amplification solutions for improved point of care diagnostics. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/72553


University of Texas – Austin

6. -1903-9795. Homeodomain proteins directly regulate ATM kinase activity.

Degree: PhD, Biochemistry, 2018, University of Texas – Austin

 The ataxia-telangiectasia mutated (ATM) kinase is a master regulator involved in the detection and repair of DNA double-strand breaks (DSBs). The Mre11/Rad50/Nbs1 (MRN) complex recruits… (more)

Subjects/Keywords: DNA repair; DNA damage; ATM; Ataxia telangiectasia; Homeodomain; MRN; Oxidative stress; Signaling

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APA (6th Edition):

-1903-9795. (2018). Homeodomain proteins directly regulate ATM kinase activity. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/9329

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

Chicago Manual of Style (16th Edition):

-1903-9795. “Homeodomain proteins directly regulate ATM kinase activity.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://dx.doi.org/10.26153/tsw/9329.

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

MLA Handbook (7th Edition):

-1903-9795. “Homeodomain proteins directly regulate ATM kinase activity.” 2018. Web. 29 Oct 2020.

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

Vancouver:

-1903-9795. Homeodomain proteins directly regulate ATM kinase activity. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2020 Oct 29]. Available from: http://dx.doi.org/10.26153/tsw/9329.

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

Council of Science Editors:

-1903-9795. Homeodomain proteins directly regulate ATM kinase activity. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://dx.doi.org/10.26153/tsw/9329

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


University of Texas – Austin

7. Villalba, Brian. Kinetic characterization of the inhibition, excision mechanisms, and fidelity of Hepatitis C Virus RNA-dependent RNA polymerase.

Degree: PhD, Biochemistry, 2020, University of Texas – Austin

 NS5B is the RNA-dependent RNA polymerase that catalyzes the replication of the Hepatitis C Virus genome. It is a major target for antiviral drugs including… (more)

Subjects/Keywords: Hepatitis C Virus; RNA polymerase; Enzyme kinetics; Nucleoside analogs

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APA (6th Edition):

Villalba, B. (2020). Kinetic characterization of the inhibition, excision mechanisms, and fidelity of Hepatitis C Virus RNA-dependent RNA polymerase. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/8952

Chicago Manual of Style (16th Edition):

Villalba, Brian. “Kinetic characterization of the inhibition, excision mechanisms, and fidelity of Hepatitis C Virus RNA-dependent RNA polymerase.” 2020. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://dx.doi.org/10.26153/tsw/8952.

MLA Handbook (7th Edition):

Villalba, Brian. “Kinetic characterization of the inhibition, excision mechanisms, and fidelity of Hepatitis C Virus RNA-dependent RNA polymerase.” 2020. Web. 29 Oct 2020.

Vancouver:

Villalba B. Kinetic characterization of the inhibition, excision mechanisms, and fidelity of Hepatitis C Virus RNA-dependent RNA polymerase. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2020. [cited 2020 Oct 29]. Available from: http://dx.doi.org/10.26153/tsw/8952.

Council of Science Editors:

Villalba B. Kinetic characterization of the inhibition, excision mechanisms, and fidelity of Hepatitis C Virus RNA-dependent RNA polymerase. [Doctoral Dissertation]. University of Texas – Austin; 2020. Available from: http://dx.doi.org/10.26153/tsw/8952


University of Texas – Austin

8. Ellefson, Jared Wade. Engineering the central dogma using emulsion based directed evolution.

Degree: PhD, Cell and molecular biology, 2016, University of Texas – Austin

 The central dogma of molecular biology forms the most basic (and fundamental) paradigm of how life operates. Despite its elegant simplicity, scientists are still uncovering… (more)

Subjects/Keywords: Directed evolution; Central dogma

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APA (6th Edition):

Ellefson, J. W. (2016). Engineering the central dogma using emulsion based directed evolution. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/39570

Chicago Manual of Style (16th Edition):

Ellefson, Jared Wade. “Engineering the central dogma using emulsion based directed evolution.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/39570.

MLA Handbook (7th Edition):

Ellefson, Jared Wade. “Engineering the central dogma using emulsion based directed evolution.” 2016. Web. 29 Oct 2020.

Vancouver:

Ellefson JW. Engineering the central dogma using emulsion based directed evolution. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/39570.

Council of Science Editors:

Ellefson JW. Engineering the central dogma using emulsion based directed evolution. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/39570


University of Texas – Austin

9. Satija, Rohit. Understanding structural transitions and dynamics in biomolecules at a single molecule level.

Degree: PhD, Cell and Molecular Biology, 2020, University of Texas – Austin

 Transition paths are fleeting events when a molecule crosses a barrier separating stable configurational basins. Recent advances in single molecule experiments, including optical tweezers-based force… (more)

Subjects/Keywords: Theoretical chemical physics; Reaction dynamics; Kinetics; Transition path time; Single molecule force spectroscopy; FRET; Subdiffusion; Non-Markovian models; Memory kernel; Loop closure; Protein folding

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APA (6th Edition):

Satija, R. (2020). Understanding structural transitions and dynamics in biomolecules at a single molecule level. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/9031

Chicago Manual of Style (16th Edition):

Satija, Rohit. “Understanding structural transitions and dynamics in biomolecules at a single molecule level.” 2020. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://dx.doi.org/10.26153/tsw/9031.

MLA Handbook (7th Edition):

Satija, Rohit. “Understanding structural transitions and dynamics in biomolecules at a single molecule level.” 2020. Web. 29 Oct 2020.

Vancouver:

Satija R. Understanding structural transitions and dynamics in biomolecules at a single molecule level. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2020. [cited 2020 Oct 29]. Available from: http://dx.doi.org/10.26153/tsw/9031.

Council of Science Editors:

Satija R. Understanding structural transitions and dynamics in biomolecules at a single molecule level. [Doctoral Dissertation]. University of Texas – Austin; 2020. Available from: http://dx.doi.org/10.26153/tsw/9031


University of Texas – Austin

10. Liu, Chien-Hung. Battle between influenza A virus and a newly identified ZAPL antiviral activity.

Degree: PhD, Microbiology, 2015, University of Texas – Austin

 Influenza A virus infection causes a highly contagious annual respiratory disease in humans as well as periodic pandemics with higher mortality rates. The Krug laboratory… (more)

Subjects/Keywords: Influenza A virus; Zinc-finger antiviral protein; Viral polymerase protein; Poly-ADP-ribosylation-dependent ubiquitination-proteasomal degradation

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APA (6th Edition):

Liu, C. (2015). Battle between influenza A virus and a newly identified ZAPL antiviral activity. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46562

Chicago Manual of Style (16th Edition):

Liu, Chien-Hung. “Battle between influenza A virus and a newly identified ZAPL antiviral activity.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/46562.

MLA Handbook (7th Edition):

Liu, Chien-Hung. “Battle between influenza A virus and a newly identified ZAPL antiviral activity.” 2015. Web. 29 Oct 2020.

Vancouver:

Liu C. Battle between influenza A virus and a newly identified ZAPL antiviral activity. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/46562.

Council of Science Editors:

Liu C. Battle between influenza A virus and a newly identified ZAPL antiviral activity. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46562


University of Texas – Austin

11. Sardana, Richa. From knobs to a central pseudoknot : understanding 40S ribosomal subunit biogenesis through Bud23.

Degree: PhD, Microbiology, 2013, University of Texas – Austin

 Ribosomes are universally conserved macromolecular machines that translate cellular genetic information into proteins. All ribosomes are com- posed of two ribonucleoprotein subunits. In eukaryotes these… (more)

Subjects/Keywords: Ribosome biogenesis; Small subunit; Central pseudoknot

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APA (6th Edition):

Sardana, R. (2013). From knobs to a central pseudoknot : understanding 40S ribosomal subunit biogenesis through Bud23. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30458

Chicago Manual of Style (16th Edition):

Sardana, Richa. “From knobs to a central pseudoknot : understanding 40S ribosomal subunit biogenesis through Bud23.” 2013. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/30458.

MLA Handbook (7th Edition):

Sardana, Richa. “From knobs to a central pseudoknot : understanding 40S ribosomal subunit biogenesis through Bud23.” 2013. Web. 29 Oct 2020.

Vancouver:

Sardana R. From knobs to a central pseudoknot : understanding 40S ribosomal subunit biogenesis through Bud23. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/30458.

Council of Science Editors:

Sardana R. From knobs to a central pseudoknot : understanding 40S ribosomal subunit biogenesis through Bud23. [Doctoral Dissertation]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/30458


University of Texas – Austin

12. Mayfield, Joshua Edward. Post-translational modification of the C-terminal domain of RNA polymerase II : identification and cross talk.

Degree: PhD, Biochemistry, 2020, University of Texas – Austin

 RNA polymerase II is a highly regulated protein complex that transcribes all protein coding mRNA and many non-coding RNAs. A key mechanism that facilitates its… (more)

Subjects/Keywords: Transcription; Post-translational modification; Phosphorylation; Proline isomerization; Mass spectrometry; Chemical biology

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APA (6th Edition):

Mayfield, J. E. (2020). Post-translational modification of the C-terminal domain of RNA polymerase II : identification and cross talk. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/7505

Chicago Manual of Style (16th Edition):

Mayfield, Joshua Edward. “Post-translational modification of the C-terminal domain of RNA polymerase II : identification and cross talk.” 2020. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://dx.doi.org/10.26153/tsw/7505.

MLA Handbook (7th Edition):

Mayfield, Joshua Edward. “Post-translational modification of the C-terminal domain of RNA polymerase II : identification and cross talk.” 2020. Web. 29 Oct 2020.

Vancouver:

Mayfield JE. Post-translational modification of the C-terminal domain of RNA polymerase II : identification and cross talk. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2020. [cited 2020 Oct 29]. Available from: http://dx.doi.org/10.26153/tsw/7505.

Council of Science Editors:

Mayfield JE. Post-translational modification of the C-terminal domain of RNA polymerase II : identification and cross talk. [Doctoral Dissertation]. University of Texas – Austin; 2020. Available from: http://dx.doi.org/10.26153/tsw/7505


University of Texas – Austin

13. -2157-1967. Kinetic studies of HIV-1 Reverse Transcriptase nucleotide selectivity, drug resistance and RNase H activity.

Degree: PhD, Biochemistry, 2018, University of Texas – Austin

 Mechanisms of nucleotide selectivity and drug resistance by HIV-1 Reverse Transcriptase (HIVRT) were examined using rapid kinetic methods and global data fitting. Thymidine analog resistance… (more)

Subjects/Keywords: HIV-1 Reverse Transcriptase; Nucleotide selectivity; TAMs and 69 insertion complex associated drug resistance; RNase H; Rate-limiting PPi release

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APA (6th Edition):

-2157-1967. (2018). Kinetic studies of HIV-1 Reverse Transcriptase nucleotide selectivity, drug resistance and RNase H activity. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68818

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

Chicago Manual of Style (16th Edition):

-2157-1967. “Kinetic studies of HIV-1 Reverse Transcriptase nucleotide selectivity, drug resistance and RNase H activity.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/68818.

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

MLA Handbook (7th Edition):

-2157-1967. “Kinetic studies of HIV-1 Reverse Transcriptase nucleotide selectivity, drug resistance and RNase H activity.” 2018. Web. 29 Oct 2020.

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

Vancouver:

-2157-1967. Kinetic studies of HIV-1 Reverse Transcriptase nucleotide selectivity, drug resistance and RNase H activity. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/68818.

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

Council of Science Editors:

-2157-1967. Kinetic studies of HIV-1 Reverse Transcriptase nucleotide selectivity, drug resistance and RNase H activity. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/68818

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


University of Texas – Austin

14. Patchett, Stephanie Ann. Investigating the consequences of human disease related mutations on 60S ribosome assembly and function in yeast.

Degree: PhD, Microbiology, 2016, University of Texas – Austin

 In actively growing yeast cells, thousands of ribosomes are synthesized per minute. After rapid assembly, these complex machines must faithfully translate mRNA into the cell’s… (more)

Subjects/Keywords: Ribosome biogenesis; Rpl10; Rpl5; Lsg1; T-ALL

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APA (6th Edition):

Patchett, S. A. (2016). Investigating the consequences of human disease related mutations on 60S ribosome assembly and function in yeast. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/72758

Chicago Manual of Style (16th Edition):

Patchett, Stephanie Ann. “Investigating the consequences of human disease related mutations on 60S ribosome assembly and function in yeast.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/72758.

MLA Handbook (7th Edition):

Patchett, Stephanie Ann. “Investigating the consequences of human disease related mutations on 60S ribosome assembly and function in yeast.” 2016. Web. 29 Oct 2020.

Vancouver:

Patchett SA. Investigating the consequences of human disease related mutations on 60S ribosome assembly and function in yeast. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/72758.

Council of Science Editors:

Patchett SA. Investigating the consequences of human disease related mutations on 60S ribosome assembly and function in yeast. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/72758


University of Texas – Austin

15. -7681-2609. Biochemical characterization of monoclonal antibodies to the Bordetella pertussis Filamentous hemagglutinin (FHA) and Pertussis toxin (PTx) : implications for improved acellular pertussis vaccine design.

Degree: PhD, Biochemistry, 2015, University of Texas – Austin

 Incidence rates of whooping cough were dramatically decreased by immunization with whole cell pertussis (wP) vaccines in the 1940s. However, concerns about the safety of… (more)

Subjects/Keywords: Acellular pertussis vaccine; Bordetella pertussis; Antibodies

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APA (6th Edition):

-7681-2609. (2015). Biochemical characterization of monoclonal antibodies to the Bordetella pertussis Filamentous hemagglutinin (FHA) and Pertussis toxin (PTx) : implications for improved acellular pertussis vaccine design. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/61768

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Chicago Manual of Style (16th Edition):

-7681-2609. “Biochemical characterization of monoclonal antibodies to the Bordetella pertussis Filamentous hemagglutinin (FHA) and Pertussis toxin (PTx) : implications for improved acellular pertussis vaccine design.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/61768.

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Author name may be incomplete

MLA Handbook (7th Edition):

-7681-2609. “Biochemical characterization of monoclonal antibodies to the Bordetella pertussis Filamentous hemagglutinin (FHA) and Pertussis toxin (PTx) : implications for improved acellular pertussis vaccine design.” 2015. Web. 29 Oct 2020.

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Author name may be incomplete

Vancouver:

-7681-2609. Biochemical characterization of monoclonal antibodies to the Bordetella pertussis Filamentous hemagglutinin (FHA) and Pertussis toxin (PTx) : implications for improved acellular pertussis vaccine design. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/61768.

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

Council of Science Editors:

-7681-2609. Biochemical characterization of monoclonal antibodies to the Bordetella pertussis Filamentous hemagglutinin (FHA) and Pertussis toxin (PTx) : implications for improved acellular pertussis vaccine design. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/61768

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


University of Texas – Austin

16. -8375-338X. Characterization of the biogenesis and function of miRNAs encoded by diverse tumor viruses.

Degree: PhD, Cell and Molecular Biology, 2016, University of Texas – Austin

 Some eukaryotic viruses express small RNAs called microRNAs (miRNAs) to regulate host and viral gene expression. Due to their small genomic footprint, ability to regulate… (more)

Subjects/Keywords: miRNA; Polyomavirus; BLV; shRNA; RNAi

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APA (6th Edition):

-8375-338X. (2016). Characterization of the biogenesis and function of miRNAs encoded by diverse tumor viruses. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68600

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

Chicago Manual of Style (16th Edition):

-8375-338X. “Characterization of the biogenesis and function of miRNAs encoded by diverse tumor viruses.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/68600.

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

MLA Handbook (7th Edition):

-8375-338X. “Characterization of the biogenesis and function of miRNAs encoded by diverse tumor viruses.” 2016. Web. 29 Oct 2020.

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

Vancouver:

-8375-338X. Characterization of the biogenesis and function of miRNAs encoded by diverse tumor viruses. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/68600.

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

Council of Science Editors:

-8375-338X. Characterization of the biogenesis and function of miRNAs encoded by diverse tumor viruses. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/68600

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


University of Texas – Austin

17. Ziehr, Jessica Lea. Kinetics and specificity of human mitochondrial DNA polymerase gamma and HIV-1 reverse transcriptase.

Degree: PhD, Cell and Molecular Biology, 2014, University of Texas – Austin

 The human mitochondrial DNA (mtDNA) genome must be faithfully maintained by the mitochondrial DNA replication machinery. Deficiencies in mtDNA maintenance result in the accumulation of… (more)

Subjects/Keywords: DNA polymerase; Pre-steady state kinetics; HIV reverse transcriptase; Polymerase gamma

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APA (6th Edition):

Ziehr, J. L. (2014). Kinetics and specificity of human mitochondrial DNA polymerase gamma and HIV-1 reverse transcriptase. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/31296

Chicago Manual of Style (16th Edition):

Ziehr, Jessica Lea. “Kinetics and specificity of human mitochondrial DNA polymerase gamma and HIV-1 reverse transcriptase.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/31296.

MLA Handbook (7th Edition):

Ziehr, Jessica Lea. “Kinetics and specificity of human mitochondrial DNA polymerase gamma and HIV-1 reverse transcriptase.” 2014. Web. 29 Oct 2020.

Vancouver:

Ziehr JL. Kinetics and specificity of human mitochondrial DNA polymerase gamma and HIV-1 reverse transcriptase. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/31296.

Council of Science Editors:

Ziehr JL. Kinetics and specificity of human mitochondrial DNA polymerase gamma and HIV-1 reverse transcriptase. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/31296


University of Texas – Austin

18. Lamech, Lilian Tawsein M. Mitochondrial tyrosyl-tRNA synthetases : evolving a function beyond translation.

Degree: PhD, Microbiology, 2014, University of Texas – Austin

 Pezizomycotina mitochondrial tyrosyl-tRNA synthetases (mtTyrRS) are bifunctional, with the ability to splice group I introns in addition to catalyzing aminoacylation. Work done with the Neurospora… (more)

Subjects/Keywords: TRNA; Tyrosyl-tRNA synthetase; CYT-18; MtTyrRS; SAXS; X-ray crystallography

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APA (6th Edition):

Lamech, L. T. M. (2014). Mitochondrial tyrosyl-tRNA synthetases : evolving a function beyond translation. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/31554

Chicago Manual of Style (16th Edition):

Lamech, Lilian Tawsein M. “Mitochondrial tyrosyl-tRNA synthetases : evolving a function beyond translation.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/31554.

MLA Handbook (7th Edition):

Lamech, Lilian Tawsein M. “Mitochondrial tyrosyl-tRNA synthetases : evolving a function beyond translation.” 2014. Web. 29 Oct 2020.

Vancouver:

Lamech LTM. Mitochondrial tyrosyl-tRNA synthetases : evolving a function beyond translation. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/31554.

Council of Science Editors:

Lamech LTM. Mitochondrial tyrosyl-tRNA synthetases : evolving a function beyond translation. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/31554


University of Texas – Austin

19. -5005-7182. Single molecule peptide sequencing.

Degree: PhD, Cell and Molecular Biology, 2015, University of Texas – Austin

 The proteome is a highly dynamic and complex set of proteins, specific not only to a particular organism, but to cell types and environmental conditions.… (more)

Subjects/Keywords: Peptide sequencing; Single molecule; Proteomics; Proteomes; Proteome changes; Fluorosequencing

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APA (6th Edition):

-5005-7182. (2015). Single molecule peptide sequencing. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/47208

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-5005-7182. “Single molecule peptide sequencing.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/47208.

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

MLA Handbook (7th Edition):

-5005-7182. “Single molecule peptide sequencing.” 2015. Web. 29 Oct 2020.

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

Vancouver:

-5005-7182. Single molecule peptide sequencing. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/47208.

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

Council of Science Editors:

-5005-7182. Single molecule peptide sequencing. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/47208

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Author name may be incomplete


University of Texas – Austin

20. Qin, Yidan. Thermostable group II intron reverse transcriptases and their applications in next generation RNA sequencing, diagnostics, and precision medicine.

Degree: PhD, Microbiology, 2016, University of Texas – Austin

 Thermostable group II intron reverse transcriptases (TGIRTs) from thermophilic bacteria are advantageous for biotechnological applications that require cDNA synthesis, such as RT-qPCR and RNA-seq. TGIRTs… (more)

Subjects/Keywords: RNA-seq; Diagnostics; Precision medicine; Non-coding RNA; Circulating RNA

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APA (6th Edition):

Qin, Y. (2016). Thermostable group II intron reverse transcriptases and their applications in next generation RNA sequencing, diagnostics, and precision medicine. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/41602

Chicago Manual of Style (16th Edition):

Qin, Yidan. “Thermostable group II intron reverse transcriptases and their applications in next generation RNA sequencing, diagnostics, and precision medicine.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/41602.

MLA Handbook (7th Edition):

Qin, Yidan. “Thermostable group II intron reverse transcriptases and their applications in next generation RNA sequencing, diagnostics, and precision medicine.” 2016. Web. 29 Oct 2020.

Vancouver:

Qin Y. Thermostable group II intron reverse transcriptases and their applications in next generation RNA sequencing, diagnostics, and precision medicine. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/41602.

Council of Science Editors:

Qin Y. Thermostable group II intron reverse transcriptases and their applications in next generation RNA sequencing, diagnostics, and precision medicine. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/41602

21. Potratz, Jeffrey Philip. Local and global investigations into DEAD-box protein function.

Degree: PhD, Biochemistry, 2012, University of Texas – Austin

 Numerous essential cellular processes, such as gene regulation and tRNA processing, are carried out by structured RNAs. While in vitro most RNAs become kinetically trapped… (more)

Subjects/Keywords: DEAD-box protein; Helicase; RNA folding; RNA chaperone

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APA (6th Edition):

Potratz, J. P. (2012). Local and global investigations into DEAD-box protein function. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/22154

Chicago Manual of Style (16th Edition):

Potratz, Jeffrey Philip. “Local and global investigations into DEAD-box protein function.” 2012. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/22154.

MLA Handbook (7th Edition):

Potratz, Jeffrey Philip. “Local and global investigations into DEAD-box protein function.” 2012. Web. 29 Oct 2020.

Vancouver:

Potratz JP. Local and global investigations into DEAD-box protein function. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2012. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/22154.

Council of Science Editors:

Potratz JP. Local and global investigations into DEAD-box protein function. [Doctoral Dissertation]. University of Texas – Austin; 2012. Available from: http://hdl.handle.net/2152/22154

22. Mitchell, David III. Characterization of folding and misfolding of the Tetrahymena thermophila group I ribozyme.

Degree: PhD, Cell and Molecular Biology, 2013, University of Texas – Austin

 The functions of many cellular RNAs require that they fold into specific three-dimensional native structures, which typically involves arranging secondary structure elements and stabilizing the… (more)

Subjects/Keywords: Structured RNA; Group I intron; Catalytic RNA; RNA folding; RNA misfolding; RNA topology

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APA (6th Edition):

Mitchell, D. I. (2013). Characterization of folding and misfolding of the Tetrahymena thermophila group I ribozyme. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/22021

Chicago Manual of Style (16th Edition):

Mitchell, David III. “Characterization of folding and misfolding of the Tetrahymena thermophila group I ribozyme.” 2013. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/22021.

MLA Handbook (7th Edition):

Mitchell, David III. “Characterization of folding and misfolding of the Tetrahymena thermophila group I ribozyme.” 2013. Web. 29 Oct 2020.

Vancouver:

Mitchell DI. Characterization of folding and misfolding of the Tetrahymena thermophila group I ribozyme. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/22021.

Council of Science Editors:

Mitchell DI. Characterization of folding and misfolding of the Tetrahymena thermophila group I ribozyme. [Doctoral Dissertation]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/22021

23. Jarmoskaite, Inga. Mechanistic studies of the RNA chaperone activities of the DEAD-box RNA helicase CYT-19.

Degree: PhD, Biochemistry, 2014, University of Texas – Austin

 Structured RNAs are pervasive in biology, spanning a functional repertoire that includes messengers, regulators of gene expression and catalysts of translation and splicing. From the… (more)

Subjects/Keywords: RNA folding; Group I intron; Tertiary structure; ATP utilization; SAXS

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APA (6th Edition):

Jarmoskaite, I. (2014). Mechanistic studies of the RNA chaperone activities of the DEAD-box RNA helicase CYT-19. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/25051

Chicago Manual of Style (16th Edition):

Jarmoskaite, Inga. “Mechanistic studies of the RNA chaperone activities of the DEAD-box RNA helicase CYT-19.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/25051.

MLA Handbook (7th Edition):

Jarmoskaite, Inga. “Mechanistic studies of the RNA chaperone activities of the DEAD-box RNA helicase CYT-19.” 2014. Web. 29 Oct 2020.

Vancouver:

Jarmoskaite I. Mechanistic studies of the RNA chaperone activities of the DEAD-box RNA helicase CYT-19. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/25051.

Council of Science Editors:

Jarmoskaite I. Mechanistic studies of the RNA chaperone activities of the DEAD-box RNA helicase CYT-19. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/25051

24. Choi, Woongsoon. Characterization of D135 group II intron ribozyme dimerization.

Degree: MA, Biochemistry, 2013, University of Texas – Austin

 Group II introns are highly structured RNAs that carry out self-splicing reactions. The multiple turnover version of one of these introns, termed the D135 ribozyme,… (more)

Subjects/Keywords: Group II intron ribozyme; Dimerization

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APA (6th Edition):

Choi, W. (2013). Characterization of D135 group II intron ribozyme dimerization. (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/21480

Chicago Manual of Style (16th Edition):

Choi, Woongsoon. “Characterization of D135 group II intron ribozyme dimerization.” 2013. Masters Thesis, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/21480.

MLA Handbook (7th Edition):

Choi, Woongsoon. “Characterization of D135 group II intron ribozyme dimerization.” 2013. Web. 29 Oct 2020.

Vancouver:

Choi W. Characterization of D135 group II intron ribozyme dimerization. [Internet] [Masters thesis]. University of Texas – Austin; 2013. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/21480.

Council of Science Editors:

Choi W. Characterization of D135 group II intron ribozyme dimerization. [Masters Thesis]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/21480

25. Chadee, Amanda Barbara. The roles of CYT-18 in folding, misfolding and structural specificity of the Tetrahymena group I ribozyme.

Degree: PhD, Cell and Molecular Biology, 2009, University of Texas – Austin

 Group I introns are structured RNAs that have been used extensively as model systems for RNA folding because they are experimentally tractable, yet complex enough… (more)

Subjects/Keywords: Group I introns; Structured RNAs; RNA folding; Tetrahymena; Core helices; Peripheral elements; Tertiary contacts; Ribozyme

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APA (6th Edition):

Chadee, A. B. (2009). The roles of CYT-18 in folding, misfolding and structural specificity of the Tetrahymena group I ribozyme. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/10615

Chicago Manual of Style (16th Edition):

Chadee, Amanda Barbara. “The roles of CYT-18 in folding, misfolding and structural specificity of the Tetrahymena group I ribozyme.” 2009. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/10615.

MLA Handbook (7th Edition):

Chadee, Amanda Barbara. “The roles of CYT-18 in folding, misfolding and structural specificity of the Tetrahymena group I ribozyme.” 2009. Web. 29 Oct 2020.

Vancouver:

Chadee AB. The roles of CYT-18 in folding, misfolding and structural specificity of the Tetrahymena group I ribozyme. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2009. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/10615.

Council of Science Editors:

Chadee AB. The roles of CYT-18 in folding, misfolding and structural specificity of the Tetrahymena group I ribozyme. [Doctoral Dissertation]. University of Texas – Austin; 2009. Available from: http://hdl.handle.net/2152/10615


University of Texas – Austin

26. Bhaskaran, Hari Prakash. Mechanistic studies of CYT-19 and related DExD/H-box proteins on folding of the Tetrahymena group I ribozyme.

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

 DExD/H-box proteins are a diverse class of proteins that are implicated in RNA and RNP remodeling. They have sequence homology to DNA helicases and share… (more)

Subjects/Keywords: Introns; Catalytic RNA; Protein folding

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APA (6th Edition):

Bhaskaran, H. P. (2008). Mechanistic studies of CYT-19 and related DExD/H-box proteins on folding of the Tetrahymena group I ribozyme. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/3980

Chicago Manual of Style (16th Edition):

Bhaskaran, Hari Prakash. “Mechanistic studies of CYT-19 and related DExD/H-box proteins on folding of the Tetrahymena group I ribozyme.” 2008. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/3980.

MLA Handbook (7th Edition):

Bhaskaran, Hari Prakash. “Mechanistic studies of CYT-19 and related DExD/H-box proteins on folding of the Tetrahymena group I ribozyme.” 2008. Web. 29 Oct 2020.

Vancouver:

Bhaskaran HP. Mechanistic studies of CYT-19 and related DExD/H-box proteins on folding of the Tetrahymena group I ribozyme. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2008. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/3980.

Council of Science Editors:

Bhaskaran HP. Mechanistic studies of CYT-19 and related DExD/H-box proteins on folding of the Tetrahymena group I ribozyme. [Doctoral Dissertation]. University of Texas – Austin; 2008. Available from: http://hdl.handle.net/2152/3980

27. Wang, Feng, Ph. D. A co-translational ubiquitination pathway for quality control of newly synthesized proteins.

Degree: PhD, Microbiology, 2014, University of Texas – Austin

 Previous studies indicated that 6%-30% of newly synthesized proteins are rapidly degraded by the ubiquitin-proteasome system. This has generally been assumed to occur post-translationally, following… (more)

Subjects/Keywords: Co-translational ubiquitination; Protein quality control; Aging

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APA (6th Edition):

Wang, Feng, P. D. (2014). A co-translational ubiquitination pathway for quality control of newly synthesized proteins. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/31556

Chicago Manual of Style (16th Edition):

Wang, Feng, Ph D. “A co-translational ubiquitination pathway for quality control of newly synthesized proteins.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/31556.

MLA Handbook (7th Edition):

Wang, Feng, Ph D. “A co-translational ubiquitination pathway for quality control of newly synthesized proteins.” 2014. Web. 29 Oct 2020.

Vancouver:

Wang, Feng PD. A co-translational ubiquitination pathway for quality control of newly synthesized proteins. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/31556.

Council of Science Editors:

Wang, Feng PD. A co-translational ubiquitination pathway for quality control of newly synthesized proteins. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/31556

28. -2780-6317. Mechanisms of target search by DNA-binding proteins.

Degree: PhD, Biochemistry, 2018, University of Texas – Austin

 All genetic information is preserved within the DNA duplex. For successful propagation of this genetic code, DNA must be accurately replicated, repaired, and transcribed. These… (more)

Subjects/Keywords: DNA repair; MMR; CRISPR; Single-Molecule; Biophysics

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APA (6th Edition):

-2780-6317. (2018). Mechanisms of target search by DNA-binding proteins. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68160

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-2780-6317. “Mechanisms of target search by DNA-binding proteins.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/68160.

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

MLA Handbook (7th Edition):

-2780-6317. “Mechanisms of target search by DNA-binding proteins.” 2018. Web. 29 Oct 2020.

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

Vancouver:

-2780-6317. Mechanisms of target search by DNA-binding proteins. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/68160.

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

Council of Science Editors:

-2780-6317. Mechanisms of target search by DNA-binding proteins. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/68160

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

29. -6810-5157. Identifying the role of the cap-binding complexes in the regulation of translation in Arabidopsis thaliana.

Degree: PhD, Biochemistry, 2017, University of Texas – Austin

 There is a fundamental gap in our understanding of the regulation of translation in plants. None of the canonical eukaryotic methods found in mammals, such… (more)

Subjects/Keywords: Arabidopsis; Kinase; Redox; Disulfide bond; Ribosome profiling; Cap-binding complex; eIF4F; eIFiso4F; eIF4G; eIFiso4G; eIF4E; eIFiso4E

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APA (6th Edition):

-6810-5157. (2017). Identifying the role of the cap-binding complexes in the regulation of translation in Arabidopsis thaliana. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63288

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

Chicago Manual of Style (16th Edition):

-6810-5157. “Identifying the role of the cap-binding complexes in the regulation of translation in Arabidopsis thaliana.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/63288.

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

MLA Handbook (7th Edition):

-6810-5157. “Identifying the role of the cap-binding complexes in the regulation of translation in Arabidopsis thaliana.” 2017. Web. 29 Oct 2020.

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

Vancouver:

-6810-5157. Identifying the role of the cap-binding complexes in the regulation of translation in Arabidopsis thaliana. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/63288.

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

Council of Science Editors:

-6810-5157. Identifying the role of the cap-binding complexes in the regulation of translation in Arabidopsis thaliana. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/63288

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

30. Lardelli, Rea Martine. Spliceosome assembly and rearrangements : understanding how snRNPs are built and helicases function.

Degree: PhD, Biochemistry, 2010, University of Texas – Austin

 Pre-mRNA splicing by the spliceosome requires the precise and regulated efforts of the five snRNAs (U1, U2, U4, U5, and U6) and numerous associated proteins.… (more)

Subjects/Keywords: DEAH-box helicases; Prp2p; Splicing; U4/U6 snRNP; Prp24p

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APA (6th Edition):

Lardelli, R. M. (2010). Spliceosome assembly and rearrangements : understanding how snRNPs are built and helicases function. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/ETD-UT-2010-08-1608

Chicago Manual of Style (16th Edition):

Lardelli, Rea Martine. “Spliceosome assembly and rearrangements : understanding how snRNPs are built and helicases function.” 2010. Doctoral Dissertation, University of Texas – Austin. Accessed October 29, 2020. http://hdl.handle.net/2152/ETD-UT-2010-08-1608.

MLA Handbook (7th Edition):

Lardelli, Rea Martine. “Spliceosome assembly and rearrangements : understanding how snRNPs are built and helicases function.” 2010. Web. 29 Oct 2020.

Vancouver:

Lardelli RM. Spliceosome assembly and rearrangements : understanding how snRNPs are built and helicases function. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2010. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2152/ETD-UT-2010-08-1608.

Council of Science Editors:

Lardelli RM. Spliceosome assembly and rearrangements : understanding how snRNPs are built and helicases function. [Doctoral Dissertation]. University of Texas – Austin; 2010. Available from: http://hdl.handle.net/2152/ETD-UT-2010-08-1608

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