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You searched for +publisher:"University of Texas – Austin" +contributor:("Whitman, Christian"). Showing records 1 – 23 of 23 total matches.

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University of Texas – Austin

1. Ko, Yeonjin. Unusual carbohydrate biosynthesis : mechanistic studies of DesII and the biosynthesis of formycin A.

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

 Carbohydrates are essential biomolecules in all living organisms. Besides serving as energy storage and structural building blocks in primary metabolism, carbohydrates represent the building blocks… (more)

Subjects/Keywords: DesII; Formycin; Formycin A; Carbohydrate biosynthesis; Biosynthetic pathways; Radical intermediates

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APA (6th Edition):

Ko, Y. (2017). Unusual carbohydrate biosynthesis : mechanistic studies of DesII and the biosynthesis of formycin A. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/47151

Chicago Manual of Style (16th Edition):

Ko, Yeonjin. “Unusual carbohydrate biosynthesis : mechanistic studies of DesII and the biosynthesis of formycin A.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed October 15, 2019. http://hdl.handle.net/2152/47151.

MLA Handbook (7th Edition):

Ko, Yeonjin. “Unusual carbohydrate biosynthesis : mechanistic studies of DesII and the biosynthesis of formycin A.” 2017. Web. 15 Oct 2019.

Vancouver:

Ko Y. Unusual carbohydrate biosynthesis : mechanistic studies of DesII and the biosynthesis of formycin A. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/2152/47151.

Council of Science Editors:

Ko Y. Unusual carbohydrate biosynthesis : mechanistic studies of DesII and the biosynthesis of formycin A. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/47151


University of Texas – Austin

2. -7139-2043. Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase β: Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase [beta].

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

 DNA bases are constantly under the damages from both outside and inside, bringing possible mutagenic changes. To elucidate the detailed mechanisms, structural method of X-ray… (more)

Subjects/Keywords: N7-methyl; N7-benzyl; C8-chloro; Guanine lesions; Human DNA polymerase β

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APA (6th Edition):

-7139-2043. (2015). Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase β: Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase [beta]. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46815

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-7139-2043. “Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase β: Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase [beta].” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed October 15, 2019. http://hdl.handle.net/2152/46815.

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Author name may be incomplete

MLA Handbook (7th Edition):

-7139-2043. “Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase β: Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase [beta].” 2015. Web. 15 Oct 2019.

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Author name may be incomplete

Vancouver:

-7139-2043. Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase β: Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase [beta]. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/2152/46815.

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

Council of Science Editors:

-7139-2043. Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase β: Structural and kinetic study of N7-methyl, N7-benzyl and C8-chloro guanine lesions using human DNA polymerase [beta]. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46815

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Author name may be incomplete


University of Texas – Austin

3. Clevenger, Kenneth David. Investigation and engineering of PvdQ, a Pseudomonas aeruginosa enzyme at the nexus of quorum sensing and iron uptake pathways.

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

 The gram-negative human pathogen Pseudomonas aeruginosa is a widespread global health concern. Two key pathways of P. aeruginosa that are involved in its infection and/or… (more)

Subjects/Keywords: NTN-hydrolase; PvdQ; Siderophore; Pyoverdine; NRPS; Quorum-sensing; Quorum-quenching; Alkylboronic acid; Boronic acid; Iron limited growth; Pseudomonas aeruginosa

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APA (6th Edition):

Clevenger, K. D. (2014). Investigation and engineering of PvdQ, a Pseudomonas aeruginosa enzyme at the nexus of quorum sensing and iron uptake pathways. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/32902

Chicago Manual of Style (16th Edition):

Clevenger, Kenneth David. “Investigation and engineering of PvdQ, a Pseudomonas aeruginosa enzyme at the nexus of quorum sensing and iron uptake pathways.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed October 15, 2019. http://hdl.handle.net/2152/32902.

MLA Handbook (7th Edition):

Clevenger, Kenneth David. “Investigation and engineering of PvdQ, a Pseudomonas aeruginosa enzyme at the nexus of quorum sensing and iron uptake pathways.” 2014. Web. 15 Oct 2019.

Vancouver:

Clevenger KD. Investigation and engineering of PvdQ, a Pseudomonas aeruginosa enzyme at the nexus of quorum sensing and iron uptake pathways. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/2152/32902.

Council of Science Editors:

Clevenger KD. Investigation and engineering of PvdQ, a Pseudomonas aeruginosa enzyme at the nexus of quorum sensing and iron uptake pathways. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/32902


University of Texas – Austin

4. Bennett, Ryan Cole. Thermal processing cyclodextrins and thermoplastic polymers for bioavailability enhancement of poorly water-soluble drugs.

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

 With the advent and utility of high throughput screening, the number of drug substances in the developmental pipeline of pharmaceutical industries that are poorly water-soluble… (more)

Subjects/Keywords: Thermal processing; Poorly water-soluble drug

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APA (6th Edition):

Bennett, R. C. (2014). Thermal processing cyclodextrins and thermoplastic polymers for bioavailability enhancement of poorly water-soluble drugs. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/31551

Chicago Manual of Style (16th Edition):

Bennett, Ryan Cole. “Thermal processing cyclodextrins and thermoplastic polymers for bioavailability enhancement of poorly water-soluble drugs.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed October 15, 2019. http://hdl.handle.net/2152/31551.

MLA Handbook (7th Edition):

Bennett, Ryan Cole. “Thermal processing cyclodextrins and thermoplastic polymers for bioavailability enhancement of poorly water-soluble drugs.” 2014. Web. 15 Oct 2019.

Vancouver:

Bennett RC. Thermal processing cyclodextrins and thermoplastic polymers for bioavailability enhancement of poorly water-soluble drugs. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/2152/31551.

Council of Science Editors:

Bennett RC. Thermal processing cyclodextrins and thermoplastic polymers for bioavailability enhancement of poorly water-soluble drugs. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/31551


University of Texas – Austin

5. -9758-983X. The design of halopyridine-based activity-based probes and mechanistic studies of succinylarginine dihydrolase.

Degree: PhD, Pharmaceutical Sciences, 2015, University of Texas – Austin

 An important design aspect of covalent inactivators is the balance between reactivity, or reversibility of reaction, with nucleophiles in solution and reactivity with nucleophiles at… (more)

Subjects/Keywords: Dimethylarginine dimethylaminohydrolase; Halopyridine; Activity-based probes; Succinylarginine dihydrolase

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APA (6th Edition):

-9758-983X. (2015). The design of halopyridine-based activity-based probes and mechanistic studies of succinylarginine dihydrolase. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46556

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-9758-983X. “The design of halopyridine-based activity-based probes and mechanistic studies of succinylarginine dihydrolase.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed October 15, 2019. http://hdl.handle.net/2152/46556.

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Author name may be incomplete

MLA Handbook (7th Edition):

-9758-983X. “The design of halopyridine-based activity-based probes and mechanistic studies of succinylarginine dihydrolase.” 2015. Web. 15 Oct 2019.

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

Vancouver:

-9758-983X. The design of halopyridine-based activity-based probes and mechanistic studies of succinylarginine dihydrolase. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/2152/46556.

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

Council of Science Editors:

-9758-983X. The design of halopyridine-based activity-based probes and mechanistic studies of succinylarginine dihydrolase. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46556

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Author name may be incomplete


University of Texas – Austin

6. -3503-3219. Syntheses of anticancer agents that target DNA : steroids, nucleosides, and platinums.

Degree: PhD, Pharmaceutical Sciences, 2017, University of Texas – Austin

 Cephalostatins from Cephalodiscus gilchristi and ritterazines from Ritterella tokioka inhibit cell growth in nanomolar concentrations by inducing unknown apoptosis pathway. Their NCI-60 growth inhibition patterns… (more)

Subjects/Keywords: Cephalostatin; Ritterazine; EZH2; 7-Deazaguanine; DNA repair; Platinum-intercalator conjugate; Interstrand crosslink

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APA (6th Edition):

-3503-3219. (2017). Syntheses of anticancer agents that target DNA : steroids, nucleosides, and platinums. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/72692

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Chicago Manual of Style (16th Edition):

-3503-3219. “Syntheses of anticancer agents that target DNA : steroids, nucleosides, and platinums.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed October 15, 2019. http://hdl.handle.net/2152/72692.

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Author name may be incomplete

MLA Handbook (7th Edition):

-3503-3219. “Syntheses of anticancer agents that target DNA : steroids, nucleosides, and platinums.” 2017. Web. 15 Oct 2019.

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

Vancouver:

-3503-3219. Syntheses of anticancer agents that target DNA : steroids, nucleosides, and platinums. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/2152/72692.

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

Council of Science Editors:

-3503-3219. Syntheses of anticancer agents that target DNA : steroids, nucleosides, and platinums. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/72692

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Author name may be incomplete


University of Texas – Austin

7. 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 15, 2019. 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. 15 Oct 2019.

Vancouver:

Wu M. DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2019 Oct 15]. 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

8. Samuel, Stevan Ashad. Exploration of novel architectures for aromatic electronic donor-acceptor hetero-duplexes.

Degree: PhD, Organic Chemistry, 2011, University of Texas – Austin

 Research within the Iverson group has been primarily focused around the investigation of aromatic donor-acceptor interactions between an electron-rich 1,5-dialkoyxnaphthalene (DAN) molecule and the electron-deficient… (more)

Subjects/Keywords: Aromatic electronic; Heteroduplex

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APA (6th Edition):

Samuel, S. A. (2011). Exploration of novel architectures for aromatic electronic donor-acceptor hetero-duplexes. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/44632

Chicago Manual of Style (16th Edition):

Samuel, Stevan Ashad. “Exploration of novel architectures for aromatic electronic donor-acceptor hetero-duplexes.” 2011. Doctoral Dissertation, University of Texas – Austin. Accessed October 15, 2019. http://hdl.handle.net/2152/44632.

MLA Handbook (7th Edition):

Samuel, Stevan Ashad. “Exploration of novel architectures for aromatic electronic donor-acceptor hetero-duplexes.” 2011. Web. 15 Oct 2019.

Vancouver:

Samuel SA. Exploration of novel architectures for aromatic electronic donor-acceptor hetero-duplexes. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2011. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/2152/44632.

Council of Science Editors:

Samuel SA. Exploration of novel architectures for aromatic electronic donor-acceptor hetero-duplexes. [Doctoral Dissertation]. University of Texas – Austin; 2011. Available from: http://hdl.handle.net/2152/44632


University of Texas – Austin

9. -9265-9181. Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides.

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

 Biosynthetic studies of natural products are essential to the discovery and development of new drugs, because by understanding biosynthetic pathways and the enzymes that characterize… (more)

Subjects/Keywords: Biosynthesis; Aminoglycoside; Radical SAM; Enzyme

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APA (6th Edition):

-9265-9181. (2016). Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68375

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-9265-9181. “Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed October 15, 2019. http://hdl.handle.net/2152/68375.

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

MLA Handbook (7th Edition):

-9265-9181. “Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides.” 2016. Web. 15 Oct 2019.

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

Vancouver:

-9265-9181. Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/2152/68375.

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

Council of Science Editors:

-9265-9181. Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/68375

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Author name may be incomplete


University of Texas – Austin

10. -7992-3267. Structure-based mechanism of hydratase-aldolases in the Type I aldolase superfamily and structures of tautomerase superfamily members.

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

 Polycyclic Aromatic Hydrocarbons (PAHs) are composed of multiple benzene-like rings and their bacterial catabolism has potential utility for bioremediation. In the breakdown of each ring,… (more)

Subjects/Keywords: Hydratase-aldolase; Naphthalene; Phenanthrene; Mycobacterium vanbaalenii PYR-1; Pseudomonas putida G7; Type I aldolase; 4-oxalocrotonate tautomerase; Cis-3-chloroacrylic acid dehalogenase; Malonate semialdehyde decarboxylase; Tautomerase superfamily

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APA (6th Edition):

-7992-3267. (2017). Structure-based mechanism of hydratase-aldolases in the Type I aldolase superfamily and structures of tautomerase superfamily members. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2230

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-7992-3267. “Structure-based mechanism of hydratase-aldolases in the Type I aldolase superfamily and structures of tautomerase superfamily members.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed October 15, 2019. http://dx.doi.org/10.26153/tsw/2230.

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Author name may be incomplete

MLA Handbook (7th Edition):

-7992-3267. “Structure-based mechanism of hydratase-aldolases in the Type I aldolase superfamily and structures of tautomerase superfamily members.” 2017. Web. 15 Oct 2019.

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

Vancouver:

-7992-3267. Structure-based mechanism of hydratase-aldolases in the Type I aldolase superfamily and structures of tautomerase superfamily members. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2019 Oct 15]. Available from: http://dx.doi.org/10.26153/tsw/2230.

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

Council of Science Editors:

-7992-3267. Structure-based mechanism of hydratase-aldolases in the Type I aldolase superfamily and structures of tautomerase superfamily members. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://dx.doi.org/10.26153/tsw/2230

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Author name may be incomplete


University of Texas – Austin

11. Liu, Cheng-Hao. Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues.

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

 Enzymes are biological catalysts which greatly accelerate the rate of chemical reactions with remarkable substrate specificity and stereoselectivity. To optimize their catalytic abilities, many enzymes… (more)

Subjects/Keywords: Enzyme mechanism; Chiral substrate; ACC deaminase; PLP; Difluorocyclopropane; Tight-binding inhibitor; IspH; chiral methyl analysis; Iron-sulfur cluster

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APA (6th Edition):

Liu, C. (2014). Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63859

Chicago Manual of Style (16th Edition):

Liu, Cheng-Hao. “Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed October 15, 2019. http://hdl.handle.net/2152/63859.

MLA Handbook (7th Edition):

Liu, Cheng-Hao. “Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues.” 2014. Web. 15 Oct 2019.

Vancouver:

Liu C. Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/2152/63859.

Council of Science Editors:

Liu C. Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/63859


University of Texas – Austin

12. Romo, Anthony James. Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin.

Degree: PhD, Pharmaceutical Sciences, 2019, University of Texas – Austin

 Advancements in our ability to obtain high quality bacterial whole genome sequences have increased the rate natural product biosynthetic gene clusters are identified, but these… (more)

Subjects/Keywords: Next generation sequencing; Peptidyl nucleoside antibiotics; Gene cluster; Streptomyces

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APA (6th Edition):

Romo, A. J. (2019). Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2198

Chicago Manual of Style (16th Edition):

Romo, Anthony James. “Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed October 15, 2019. http://dx.doi.org/10.26153/tsw/2198.

MLA Handbook (7th Edition):

Romo, Anthony James. “Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin.” 2019. Web. 15 Oct 2019.

Vancouver:

Romo AJ. Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2019 Oct 15]. Available from: http://dx.doi.org/10.26153/tsw/2198.

Council of Science Editors:

Romo AJ. Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/2198

13. -9681-2721. On the reactions of trans-3-chloroacrylic acid dehalogenase and a cis-3-chloroacrylic acid dehalogenase homologue, Cg10062 : mechanistic and evolutionary implications.

Degree: PhD, Pharmaceutical Sciences, 2015, University of Texas – Austin

 The tautomerase superfamily (TSF) provides an excellent model system to study enzyme specificity, catalysis, and divergent evolution. trans-3-Cholroacrylic acid dehalogenase (CaaD), cis-3-chloroacrylic acid dehalogenase (cis-CaaD),… (more)

Subjects/Keywords: Enzymes; Kinetics; Divergent evolution

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APA (6th Edition):

-9681-2721. (2015). On the reactions of trans-3-chloroacrylic acid dehalogenase and a cis-3-chloroacrylic acid dehalogenase homologue, Cg10062 : mechanistic and evolutionary implications. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30531

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-9681-2721. “On the reactions of trans-3-chloroacrylic acid dehalogenase and a cis-3-chloroacrylic acid dehalogenase homologue, Cg10062 : mechanistic and evolutionary implications.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed October 15, 2019. http://hdl.handle.net/2152/30531.

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Author name may be incomplete

MLA Handbook (7th Edition):

-9681-2721. “On the reactions of trans-3-chloroacrylic acid dehalogenase and a cis-3-chloroacrylic acid dehalogenase homologue, Cg10062 : mechanistic and evolutionary implications.” 2015. Web. 15 Oct 2019.

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

Vancouver:

-9681-2721. On the reactions of trans-3-chloroacrylic acid dehalogenase and a cis-3-chloroacrylic acid dehalogenase homologue, Cg10062 : mechanistic and evolutionary implications. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/2152/30531.

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

Council of Science Editors:

-9681-2721. On the reactions of trans-3-chloroacrylic acid dehalogenase and a cis-3-chloroacrylic acid dehalogenase homologue, Cg10062 : mechanistic and evolutionary implications. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/30531

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University of Texas – Austin

14. Sun, He, Ph. D. Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways.

Degree: PhD, Pharmaceutical Sciences, 2013, University of Texas – Austin

 The diverse reactions that enzymes catalyze have fascinated enzymologists for decades. Continuing investigations in the biosynthesis of both primary and secondary metabolites have led to… (more)

Subjects/Keywords: Unusual; Catalysis; Enzyme; Biosynthesis; Mechanism; Characterization; UDP-galactopyranose mutase; Sulfur carrier protein activating enzyme; Cobalamin-dependent radical S-adenosyl-L-methionine enzymes

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APA (6th Edition):

Sun, He, P. D. (2013). Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63875

Chicago Manual of Style (16th Edition):

Sun, He, Ph D. “Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways.” 2013. Doctoral Dissertation, University of Texas – Austin. Accessed October 15, 2019. http://hdl.handle.net/2152/63875.

MLA Handbook (7th Edition):

Sun, He, Ph D. “Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways.” 2013. Web. 15 Oct 2019.

Vancouver:

Sun, He PD. Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/2152/63875.

Council of Science Editors:

Sun, He PD. Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways. [Doctoral Dissertation]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/63875


University of Texas – Austin

15. Lin, Chia-I. Biosynthetic studies of lincomycin A, a thiosugar-containing natural product.

Degree: PhD, Chemistry, 2019, University of Texas – Austin

 The dissertation describes biosynthetic studies of lincomycin A, a thiosugarcontaining natural product. Lincomycin A was isolated from Streptomyces lincolnensis and has been used clinically as… (more)

Subjects/Keywords: Biosynthesis; Lincomycin; Thiosugar

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APA (6th Edition):

Lin, C. (2019). Biosynthetic studies of lincomycin A, a thiosugar-containing natural product. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2237

Chicago Manual of Style (16th Edition):

Lin, Chia-I. “Biosynthetic studies of lincomycin A, a thiosugar-containing natural product.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed October 15, 2019. http://dx.doi.org/10.26153/tsw/2237.

MLA Handbook (7th Edition):

Lin, Chia-I. “Biosynthetic studies of lincomycin A, a thiosugar-containing natural product.” 2019. Web. 15 Oct 2019.

Vancouver:

Lin C. Biosynthetic studies of lincomycin A, a thiosugar-containing natural product. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2019 Oct 15]. Available from: http://dx.doi.org/10.26153/tsw/2237.

Council of Science Editors:

Lin C. Biosynthetic studies of lincomycin A, a thiosugar-containing natural product. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/2237

16. Darty, Joseph Edward. Random and rational evolution of tautomerase superfamily members : analysis and implications.

Degree: PhD, Biochemistry, 2008, University of Texas – Austin

 P[Kappa]a is not responsible for the improved activity. Hence, stabilization of an enediolate intermediate may be important for catalysis. In the second part of this… (more)

Subjects/Keywords: Tautomerase superfamily; Homologous proteins; Amino terminal proline; CaaD activity

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APA (6th Edition):

Darty, J. E. (2008). Random and rational evolution of tautomerase superfamily members : analysis and implications. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/23942

Chicago Manual of Style (16th Edition):

Darty, Joseph Edward. “Random and rational evolution of tautomerase superfamily members : analysis and implications.” 2008. Doctoral Dissertation, University of Texas – Austin. Accessed October 15, 2019. http://hdl.handle.net/2152/23942.

MLA Handbook (7th Edition):

Darty, Joseph Edward. “Random and rational evolution of tautomerase superfamily members : analysis and implications.” 2008. Web. 15 Oct 2019.

Vancouver:

Darty JE. Random and rational evolution of tautomerase superfamily members : analysis and implications. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2008. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/2152/23942.

Council of Science Editors:

Darty JE. Random and rational evolution of tautomerase superfamily members : analysis and implications. [Doctoral Dissertation]. University of Texas – Austin; 2008. Available from: http://hdl.handle.net/2152/23942

17. Kim, Mu-yong. Design and biological evaluation of novel antitumor agents with mechanisms of action against topoisomerase II and/or G-quadruplexes.

Degree: PhD, Pharmacy, 2002, University of Texas – Austin

 DNA is the molecular target for many of the alkylating agents that are used in the clinic and which have significantly increased the survival rate… (more)

Subjects/Keywords: Antineoplastic agents – Design; Antineoplastic agents – Mechanism of action

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APA (6th Edition):

Kim, M. (2002). Design and biological evaluation of novel antitumor agents with mechanisms of action against topoisomerase II and/or G-quadruplexes. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/699

Chicago Manual of Style (16th Edition):

Kim, Mu-yong. “Design and biological evaluation of novel antitumor agents with mechanisms of action against topoisomerase II and/or G-quadruplexes.” 2002. Doctoral Dissertation, University of Texas – Austin. Accessed October 15, 2019. http://hdl.handle.net/2152/699.

MLA Handbook (7th Edition):

Kim, Mu-yong. “Design and biological evaluation of novel antitumor agents with mechanisms of action against topoisomerase II and/or G-quadruplexes.” 2002. Web. 15 Oct 2019.

Vancouver:

Kim M. Design and biological evaluation of novel antitumor agents with mechanisms of action against topoisomerase II and/or G-quadruplexes. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2002. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/2152/699.

Council of Science Editors:

Kim M. Design and biological evaluation of novel antitumor agents with mechanisms of action against topoisomerase II and/or G-quadruplexes. [Doctoral Dissertation]. University of Texas – Austin; 2002. Available from: http://hdl.handle.net/2152/699

18. -3965-1137. Enzyme promiscuity : a review on select tautomerase superfamily members.

Degree: MSin Pharmaceutical Sciences, Pharmaceutical sciences, 2016, University of Texas – Austin

 Enzymes are categorized into families based on sequence similarity and conserved features. Superfamilies are composed of families of enzymes with common folds and conserved features.… (more)

Subjects/Keywords: 4-oxalocrotonate tautomerase; Enzyme superfamilies; Malonate semialdehyde decarboxylase; 3-chloroacrylic dehalogenase

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APA (6th Edition):

-3965-1137. (2016). Enzyme promiscuity : a review on select tautomerase superfamily members. (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/41721

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-3965-1137. “Enzyme promiscuity : a review on select tautomerase superfamily members.” 2016. Masters Thesis, University of Texas – Austin. Accessed October 15, 2019. http://hdl.handle.net/2152/41721.

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

MLA Handbook (7th Edition):

-3965-1137. “Enzyme promiscuity : a review on select tautomerase superfamily members.” 2016. Web. 15 Oct 2019.

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

Vancouver:

-3965-1137. Enzyme promiscuity : a review on select tautomerase superfamily members. [Internet] [Masters thesis]. University of Texas – Austin; 2016. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/2152/41721.

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

Council of Science Editors:

-3965-1137. Enzyme promiscuity : a review on select tautomerase superfamily members. [Masters Thesis]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/41721

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Author name may be incomplete

19. -6306-7187. Synthesis of isosteric analogues of rooperol.

Degree: MSin Pharmaceutical Sciences, Pharmaceutical Sciences, 2017, University of Texas – Austin

 Hypoxoside is a norlignan bisglycoside derived from Hypoxis hemerocallidae (African potato), a medicinal plant used in Africa to treat a variety of disorders, including cancer,… (more)

Subjects/Keywords: Rooperol; Hypoxoside; Catechol; Natural products; Glucosides; Prodrug

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APA (6th Edition):

-6306-7187. (2017). Synthesis of isosteric analogues of rooperol. (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/47298

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-6306-7187. “Synthesis of isosteric analogues of rooperol.” 2017. Masters Thesis, University of Texas – Austin. Accessed October 15, 2019. http://hdl.handle.net/2152/47298.

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

MLA Handbook (7th Edition):

-6306-7187. “Synthesis of isosteric analogues of rooperol.” 2017. Web. 15 Oct 2019.

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

Vancouver:

-6306-7187. Synthesis of isosteric analogues of rooperol. [Internet] [Masters thesis]. University of Texas – Austin; 2017. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/2152/47298.

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

Council of Science Editors:

-6306-7187. Synthesis of isosteric analogues of rooperol. [Masters Thesis]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/47298

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

20. Burstein, Gayle Diane. An investigation of the irreversible inhibition of human N[superscript ω], N[superscript ω]- dimethylarginine dimethylaminohydrolase (DDAH1).

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

 Nitric oxide synthases (NOS) are responsible for the production of nitric oxide (NO), an essential cell-signaling molecule, in mammals. There are three isoforms of NOS… (more)

Subjects/Keywords: Enzymology; Dimethylarginine; Nitric oxide; Covalent inhibition; Drug design; DDAH1; Nitroxyl; ADMA; Chloroacetamidine

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APA (6th Edition):

Burstein, G. D. (2014). An investigation of the irreversible inhibition of human N[superscript ω], N[superscript ω]- dimethylarginine dimethylaminohydrolase (DDAH1). (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/31281

Chicago Manual of Style (16th Edition):

Burstein, Gayle Diane. “An investigation of the irreversible inhibition of human N[superscript ω], N[superscript ω]- dimethylarginine dimethylaminohydrolase (DDAH1).” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed October 15, 2019. http://hdl.handle.net/2152/31281.

MLA Handbook (7th Edition):

Burstein, Gayle Diane. “An investigation of the irreversible inhibition of human N[superscript ω], N[superscript ω]- dimethylarginine dimethylaminohydrolase (DDAH1).” 2014. Web. 15 Oct 2019.

Vancouver:

Burstein GD. An investigation of the irreversible inhibition of human N[superscript ω], N[superscript ω]- dimethylarginine dimethylaminohydrolase (DDAH1). [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/2152/31281.

Council of Science Editors:

Burstein GD. An investigation of the irreversible inhibition of human N[superscript ω], N[superscript ω]- dimethylarginine dimethylaminohydrolase (DDAH1). [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/31281

21. -8603-1251. Structural dynamics and inhibition of Hepatitis C RNA-dependent RNA polymerase.

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

 Combination therapy with direct-acting antivirals including nucleotide analogs (NAs) and non-nucleoside inhibitors (NNIs) targeting the RNA-dependent RNA polymerase NS5B have seen recent advancements and have… (more)

Subjects/Keywords: HCV; NS5B; Viral polymerase; RNA replication; Hepatitis C treatment; Hepatitis C virus; Nucleotide analogs; Non-nucleoside inhibitors; Inhibition mechanisms

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APA (6th Edition):

-8603-1251. (2017). Structural dynamics and inhibition of Hepatitis C RNA-dependent RNA polymerase. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/47432

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-8603-1251. “Structural dynamics and inhibition of Hepatitis C RNA-dependent RNA polymerase.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed October 15, 2019. http://hdl.handle.net/2152/47432.

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Author name may be incomplete

MLA Handbook (7th Edition):

-8603-1251. “Structural dynamics and inhibition of Hepatitis C RNA-dependent RNA polymerase.” 2017. Web. 15 Oct 2019.

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

Vancouver:

-8603-1251. Structural dynamics and inhibition of Hepatitis C RNA-dependent RNA polymerase. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/2152/47432.

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

Council of Science Editors:

-8603-1251. Structural dynamics and inhibition of Hepatitis C RNA-dependent RNA polymerase. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/47432

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Author name may be incomplete

22. Lin, Ke-Yi. Molecular mechanism of poly(ADP-ribosyl)ation catalyzed by human poly(ADP-ribose) polymerase-1.

Degree: PhD, Pharmaceutical Sciences, 2015, University of Texas – Austin

 Human poly(ADP-ribose) polymerase-1 (PARP-1) is an abundant nuclear enzyme which catalyzes protein poly(ADP-ribosyl)ation upon binding to DNA. NAD+ is used as a co-substrate in the… (more)

Subjects/Keywords: PARP-1; Poly(ADP-ribosyl)ation; Enzyme mechanism; Single-molecule

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APA (6th Edition):

Lin, K. (2015). Molecular mechanism of poly(ADP-ribosyl)ation catalyzed by human poly(ADP-ribose) polymerase-1. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/62239

Chicago Manual of Style (16th Edition):

Lin, Ke-Yi. “Molecular mechanism of poly(ADP-ribosyl)ation catalyzed by human poly(ADP-ribose) polymerase-1.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed October 15, 2019. http://hdl.handle.net/2152/62239.

MLA Handbook (7th Edition):

Lin, Ke-Yi. “Molecular mechanism of poly(ADP-ribosyl)ation catalyzed by human poly(ADP-ribose) polymerase-1.” 2015. Web. 15 Oct 2019.

Vancouver:

Lin K. Molecular mechanism of poly(ADP-ribosyl)ation catalyzed by human poly(ADP-ribose) polymerase-1. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/2152/62239.

Council of Science Editors:

Lin K. Molecular mechanism of poly(ADP-ribosyl)ation catalyzed by human poly(ADP-ribose) polymerase-1. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/62239


University of Texas – Austin

23. Lee, Jung Chull. Structural studies of ribosomal RNA based on cross-analysis of comparative models and three-dimensional crystal structures.

Degree: PhD, Pharmacy, 2003, University of Texas – Austin

 Basepair mapping of the rRNAs in the high-resolution crystal structures of the Thermus thermophilus 30S and Haloarcula marismortui 50S ribosomal subunits not only proved the… (more)

Subjects/Keywords: Ribosomes; RNA; Crystallography

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APA (6th Edition):

Lee, J. C. (2003). Structural studies of ribosomal RNA based on cross-analysis of comparative models and three-dimensional crystal structures. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/731

Chicago Manual of Style (16th Edition):

Lee, Jung Chull. “Structural studies of ribosomal RNA based on cross-analysis of comparative models and three-dimensional crystal structures.” 2003. Doctoral Dissertation, University of Texas – Austin. Accessed October 15, 2019. http://hdl.handle.net/2152/731.

MLA Handbook (7th Edition):

Lee, Jung Chull. “Structural studies of ribosomal RNA based on cross-analysis of comparative models and three-dimensional crystal structures.” 2003. Web. 15 Oct 2019.

Vancouver:

Lee JC. Structural studies of ribosomal RNA based on cross-analysis of comparative models and three-dimensional crystal structures. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2003. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/2152/731.

Council of Science Editors:

Lee JC. Structural studies of ribosomal RNA based on cross-analysis of comparative models and three-dimensional crystal structures. [Doctoral Dissertation]. University of Texas – Austin; 2003. Available from: http://hdl.handle.net/2152/731

.