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You searched for +publisher:"University of Texas – Austin" +contributor:("Iverson, Brent"). Showing records 1 – 18 of 18 total matches.

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University of Texas – Austin

1. Smith, Amy Rhoden. Advances in DNA binding by threading polyintercalation.

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

 Although molecules that bind DNA have the potential to modify gene expression, the reality of targeting DNA in a sequence-specific manner is still a problematic… (more)

Subjects/Keywords: DNA binding; Threading polyintercalation; Naphthalene diimide (NDI); DNase I footprinting

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APA (6th Edition):

Smith, A. R. (2013). Advances in DNA binding by threading polyintercalation. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/28690

Chicago Manual of Style (16th Edition):

Smith, Amy Rhoden. “Advances in DNA binding by threading polyintercalation.” 2013. Doctoral Dissertation, University of Texas – Austin. Accessed September 21, 2019. http://hdl.handle.net/2152/28690.

MLA Handbook (7th Edition):

Smith, Amy Rhoden. “Advances in DNA binding by threading polyintercalation.” 2013. Web. 21 Sep 2019.

Vancouver:

Smith AR. Advances in DNA binding by threading polyintercalation. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/2152/28690.

Council of Science Editors:

Smith AR. Advances in DNA binding by threading polyintercalation. [Doctoral Dissertation]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/28690


University of Texas – Austin

2. -8746-9279. Pendant NDI bisintercalator derivatives.

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

 Sequence specific binding of DNA by small molecules potentially offers the ability to control gene expression. In the past, our laboratory has developed sequence specific… (more)

Subjects/Keywords: NDI; Pendant; Intercalator; Intercalation

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APA (6th Edition):

-8746-9279. (2017). Pendant NDI bisintercalator derivatives. (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/62852

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-8746-9279. “Pendant NDI bisintercalator derivatives.” 2017. Masters Thesis, University of Texas – Austin. Accessed September 21, 2019. http://hdl.handle.net/2152/62852.

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

MLA Handbook (7th Edition):

-8746-9279. “Pendant NDI bisintercalator derivatives.” 2017. Web. 21 Sep 2019.

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

Vancouver:

-8746-9279. Pendant NDI bisintercalator derivatives. [Internet] [Masters thesis]. University of Texas – Austin; 2017. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/2152/62852.

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

Council of Science Editors:

-8746-9279. Pendant NDI bisintercalator derivatives. [Masters Thesis]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/62852

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


University of Texas – Austin

3. Kim, Mary M. Towards the synthesis of notoamide C.

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

 Members of the prenylated indole alkaloid family have attracted much attention from synthetic chemists and drug developers for their distinct structural complexity and diverse bioactivity.… (more)

Subjects/Keywords: Reverse prenylation; Notoamide C

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APA (6th Edition):

Kim, M. M. (2013). Towards the synthesis of notoamide C. (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/41447

Chicago Manual of Style (16th Edition):

Kim, Mary M. “Towards the synthesis of notoamide C.” 2013. Masters Thesis, University of Texas – Austin. Accessed September 21, 2019. http://hdl.handle.net/2152/41447.

MLA Handbook (7th Edition):

Kim, Mary M. “Towards the synthesis of notoamide C.” 2013. Web. 21 Sep 2019.

Vancouver:

Kim MM. Towards the synthesis of notoamide C. [Internet] [Masters thesis]. University of Texas – Austin; 2013. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/2152/41447.

Council of Science Editors:

Kim MM. Towards the synthesis of notoamide C. [Masters Thesis]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/41447


University of Texas – Austin

4. Eckes, Kevin Michael. Probing the effects of backbone ester substitution on self-assembly and biological activity of short depsipeptides.

Degree: PhD, Biomedical Engineering, 2015, University of Texas – Austin

 Hydrogel materials composed of self-assembled amphiphilic peptides show great promise for use as injectable, highly biocompatible biomaterials for tissue regeneration applications. However, peptides do not… (more)

Subjects/Keywords: Self-assembling biomaterials; Peptide self-assembly; Peptidomimetic materials; Depsipeptides

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APA (6th Edition):

Eckes, K. M. (2015). Probing the effects of backbone ester substitution on self-assembly and biological activity of short depsipeptides. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46551

Chicago Manual of Style (16th Edition):

Eckes, Kevin Michael. “Probing the effects of backbone ester substitution on self-assembly and biological activity of short depsipeptides.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed September 21, 2019. http://hdl.handle.net/2152/46551.

MLA Handbook (7th Edition):

Eckes, Kevin Michael. “Probing the effects of backbone ester substitution on self-assembly and biological activity of short depsipeptides.” 2015. Web. 21 Sep 2019.

Vancouver:

Eckes KM. Probing the effects of backbone ester substitution on self-assembly and biological activity of short depsipeptides. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/2152/46551.

Council of Science Editors:

Eckes KM. Probing the effects of backbone ester substitution on self-assembly and biological activity of short depsipeptides. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46551


University of Texas – Austin

5. -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

Note: this citation may be lacking information needed for this citation format:
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 September 21, 2019. http://hdl.handle.net/2152/46815.

Note: this citation may be lacking information needed for this citation format:
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. 21 Sep 2019.

Note: this citation may be lacking information needed for this citation format:
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 Sep 21]. 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

6. Paley, Olga M. Engineering a novel human methionine degrading enzyme as a broadly effective cancer therapeutic.

Degree: PhD, Chemical Engineering, 2014, University of Texas – Austin

 Many cancers have long been known to display an absolute requirement for the amino acid methionine (L-Met). Studies have shown that in the absence of… (more)

Subjects/Keywords: Protein engineering; Enzyme engineering; Cancer; Melanoma; Neuroblastoma; Prostate carcinoma; Genetic selection; Protein therapeutic

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APA (6th Edition):

Paley, O. M. (2014). Engineering a novel human methionine degrading enzyme as a broadly effective cancer therapeutic. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/31302

Chicago Manual of Style (16th Edition):

Paley, Olga M. “Engineering a novel human methionine degrading enzyme as a broadly effective cancer therapeutic.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed September 21, 2019. http://hdl.handle.net/2152/31302.

MLA Handbook (7th Edition):

Paley, Olga M. “Engineering a novel human methionine degrading enzyme as a broadly effective cancer therapeutic.” 2014. Web. 21 Sep 2019.

Vancouver:

Paley OM. Engineering a novel human methionine degrading enzyme as a broadly effective cancer therapeutic. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/2152/31302.

Council of Science Editors:

Paley OM. Engineering a novel human methionine degrading enzyme as a broadly effective cancer therapeutic. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/31302


University of Texas – Austin

7. -5387-6362. The mechanism study of fumitremorgin B dioxygenase and engineered human cystathionine gamma lyase.

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

 Peroxy-containing compounds represent a large class of natural products with many demonstrated beneficial effects to human health. Yet, very little is known about how endoperoxide… (more)

Subjects/Keywords: Endoperoxide formation; Tyrosyl radical; Non-heme iron protein; Novel α-ketoglutarate binding orientation; CGS-like protein; Engineered enzyme; Salt dependence; Substrate selectivity shift

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APA (6th Edition):

-5387-6362. (2018). The mechanism study of fumitremorgin B dioxygenase and engineered human cystathionine gamma lyase. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68396

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

Chicago Manual of Style (16th Edition):

-5387-6362. “The mechanism study of fumitremorgin B dioxygenase and engineered human cystathionine gamma lyase.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed September 21, 2019. http://hdl.handle.net/2152/68396.

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

MLA Handbook (7th Edition):

-5387-6362. “The mechanism study of fumitremorgin B dioxygenase and engineered human cystathionine gamma lyase.” 2018. Web. 21 Sep 2019.

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

Vancouver:

-5387-6362. The mechanism study of fumitremorgin B dioxygenase and engineered human cystathionine gamma lyase. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/2152/68396.

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

Council of Science Editors:

-5387-6362. The mechanism study of fumitremorgin B dioxygenase and engineered human cystathionine gamma lyase. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/68396

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


University of Texas – Austin

8. -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

Note: this citation may be lacking information needed for this citation format:
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 September 21, 2019. http://hdl.handle.net/2152/46556.

Note: this citation may be lacking information needed for this citation format:
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. 21 Sep 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 Sep 21]. 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

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


University of Texas – Austin

9. Ikkanda, Brian Aki. Assembly of complimentary naphthyl units in nucleotidomimetic foldamers.

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

 The large and complex architectures found in biomolecules not only are an amazing feat of molecular construction, but they also function to carry out all… (more)

Subjects/Keywords: Aromatic; DNA; Deoxyribonucleic acid; DAN; NDI; Foldamer; Organic chemistry; Bioorganic chemistry; Chemical biology

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APA (6th Edition):

Ikkanda, B. A. (2016). Assembly of complimentary naphthyl units in nucleotidomimetic foldamers. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68382

Chicago Manual of Style (16th Edition):

Ikkanda, Brian Aki. “Assembly of complimentary naphthyl units in nucleotidomimetic foldamers.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed September 21, 2019. http://hdl.handle.net/2152/68382.

MLA Handbook (7th Edition):

Ikkanda, Brian Aki. “Assembly of complimentary naphthyl units in nucleotidomimetic foldamers.” 2016. Web. 21 Sep 2019.

Vancouver:

Ikkanda BA. Assembly of complimentary naphthyl units in nucleotidomimetic foldamers. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/2152/68382.

Council of Science Editors:

Ikkanda BA. Assembly of complimentary naphthyl units in nucleotidomimetic foldamers. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/68382

10. Diehl, Katharine Louise. Development of cross-reactive receptors based on serum albumin.

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

 In recent years, differential sensing has become an increasingly popular approach to molecular recognition. Mimicking the mammalian senses of taste and smell, arrays of semi-selective… (more)

Subjects/Keywords: Array sensing; Chemometrics; Glyceride; Squaraine; Conjugate acceptor; Serum albumin

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APA (6th Edition):

Diehl, K. L. (2015). Development of cross-reactive receptors based on serum albumin. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46543

Chicago Manual of Style (16th Edition):

Diehl, Katharine Louise. “Development of cross-reactive receptors based on serum albumin.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed September 21, 2019. http://hdl.handle.net/2152/46543.

MLA Handbook (7th Edition):

Diehl, Katharine Louise. “Development of cross-reactive receptors based on serum albumin.” 2015. Web. 21 Sep 2019.

Vancouver:

Diehl KL. Development of cross-reactive receptors based on serum albumin. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/2152/46543.

Council of Science Editors:

Diehl KL. Development of cross-reactive receptors based on serum albumin. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46543


University of Texas – Austin

11. Peebles, Cameron David. Conformational switching within aromatic, electron donor and acceptor supramolecular architectures.

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

 The Iverson group has utilized favorable interactions between aromatic units in the development of highly ordered amphiphilic foldamers, two-component liquid crystal assemblies and pseudo-DNA assemblies.… (more)

Subjects/Keywords: Supramolecular donor-acceptor; Aromatic units; Aromatic stacking; Conformational switching; Amphiphilic foldamers; Polymers

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APA (6th Edition):

Peebles, C. D. (2015). Conformational switching within aromatic, electron donor and acceptor supramolecular architectures. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46704

Chicago Manual of Style (16th Edition):

Peebles, Cameron David. “Conformational switching within aromatic, electron donor and acceptor supramolecular architectures.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed September 21, 2019. http://hdl.handle.net/2152/46704.

MLA Handbook (7th Edition):

Peebles, Cameron David. “Conformational switching within aromatic, electron donor and acceptor supramolecular architectures.” 2015. Web. 21 Sep 2019.

Vancouver:

Peebles CD. Conformational switching within aromatic, electron donor and acceptor supramolecular architectures. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/2152/46704.

Council of Science Editors:

Peebles CD. Conformational switching within aromatic, electron donor and acceptor supramolecular architectures. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46704


University of Texas – Austin

12. 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 September 21, 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. 21 Sep 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 Sep 21]. 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

13. Pogson, Mark Wilson. Next generation approaches toward engineering therapeutic proteases.

Degree: PhD, Cell and Molecular Biology, 2012, University of Texas – Austin

 Engineering protease substrate specificity and selectivity has the potential to yield entirely new possibilities in the analytical, biotechnological, and therapeutic domains. For example, therapeutic applications… (more)

Subjects/Keywords: Proteases; Protein engineering; FACS; High-throughput screening; Biotechnology

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APA (6th Edition):

Pogson, M. W. (2012). Next generation approaches toward engineering therapeutic proteases. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/22152

Chicago Manual of Style (16th Edition):

Pogson, Mark Wilson. “Next generation approaches toward engineering therapeutic proteases.” 2012. Doctoral Dissertation, University of Texas – Austin. Accessed September 21, 2019. http://hdl.handle.net/2152/22152.

MLA Handbook (7th Edition):

Pogson, Mark Wilson. “Next generation approaches toward engineering therapeutic proteases.” 2012. Web. 21 Sep 2019.

Vancouver:

Pogson MW. Next generation approaches toward engineering therapeutic proteases. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2012. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/2152/22152.

Council of Science Editors:

Pogson MW. Next generation approaches toward engineering therapeutic proteases. [Doctoral Dissertation]. University of Texas – Austin; 2012. Available from: http://hdl.handle.net/2152/22152

14. Long, Samuel Reid. Studies of multicomponent assemblies.

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

 This dissertation is divided into three major sections (one on dendrimers, one on tripodal metal ligands and one on a research oriented chemistry curricula) with… (more)

Subjects/Keywords: Multicomponent assemblies; Cooperativity; PAMAM dendrimer; Reversible covalent bond formation; Teaching through research; Sensing; Research oriented labs; FRI

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APA (6th Edition):

Long, S. R. (2012). Studies of multicomponent assemblies. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/23392

Chicago Manual of Style (16th Edition):

Long, Samuel Reid. “Studies of multicomponent assemblies.” 2012. Doctoral Dissertation, University of Texas – Austin. Accessed September 21, 2019. http://hdl.handle.net/2152/23392.

MLA Handbook (7th Edition):

Long, Samuel Reid. “Studies of multicomponent assemblies.” 2012. Web. 21 Sep 2019.

Vancouver:

Long SR. Studies of multicomponent assemblies. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2012. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/2152/23392.

Council of Science Editors:

Long SR. Studies of multicomponent assemblies. [Doctoral Dissertation]. University of Texas – Austin; 2012. Available from: http://hdl.handle.net/2152/23392


University of Texas – Austin

15. Lee, Jeeyeon. Toward threading polyintercalators with programmed sequence specificity.

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

Subjects/Keywords: Molecular recognition; DNA-protein interactions

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APA (6th Edition):

Lee, J. (2003). Toward threading polyintercalators with programmed sequence specificity. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/732

Chicago Manual of Style (16th Edition):

Lee, Jeeyeon. “Toward threading polyintercalators with programmed sequence specificity.” 2003. Doctoral Dissertation, University of Texas – Austin. Accessed September 21, 2019. http://hdl.handle.net/2152/732.

MLA Handbook (7th Edition):

Lee, Jeeyeon. “Toward threading polyintercalators with programmed sequence specificity.” 2003. Web. 21 Sep 2019.

Vancouver:

Lee J. Toward threading polyintercalators with programmed sequence specificity. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2003. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/2152/732.

Council of Science Editors:

Lee J. Toward threading polyintercalators with programmed sequence specificity. [Doctoral Dissertation]. University of Texas – Austin; 2003. Available from: http://hdl.handle.net/2152/732

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

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 September 21, 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. 21 Sep 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 Sep 21]. 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

17. Jewett, Ivan Tucker. Development of iminium ion cascade methodologies and their application to the synthesis of complex molecules.

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

 In the interests of synthetic efficiency several cascade reactions involving iminium ion intermediates have developed to allow for the rapid assembly of complex molecules from… (more)

Subjects/Keywords: Iminium ion; Cascade reactions; Quinolizidine; Alkaloid; Actinophyllic acid

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

APA (6th Edition):

Jewett, I. T. (2010). Development of iminium ion cascade methodologies and their application to the synthesis of complex molecules. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30932

Chicago Manual of Style (16th Edition):

Jewett, Ivan Tucker. “Development of iminium ion cascade methodologies and their application to the synthesis of complex molecules.” 2010. Doctoral Dissertation, University of Texas – Austin. Accessed September 21, 2019. http://hdl.handle.net/2152/30932.

MLA Handbook (7th Edition):

Jewett, Ivan Tucker. “Development of iminium ion cascade methodologies and their application to the synthesis of complex molecules.” 2010. Web. 21 Sep 2019.

Vancouver:

Jewett IT. Development of iminium ion cascade methodologies and their application to the synthesis of complex molecules. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2010. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/2152/30932.

Council of Science Editors:

Jewett IT. Development of iminium ion cascade methodologies and their application to the synthesis of complex molecules. [Doctoral Dissertation]. University of Texas – Austin; 2010. Available from: http://hdl.handle.net/2152/30932

18. Chrysostomou, Constantine. Addressing intrinsic challenges for next generation sequencing of immunoglobulin repertoires.

Degree: PhD, Chemical Engineering, 2014, University of Texas – Austin

 Antibodies are essential molecules that help to provide immunity against a vast population of environmental pathogens. This antibody conferred protection is dependent upon genetic diversification… (more)

Subjects/Keywords: Next generation sequencing; Immunology; Repertoires; Statistical analyses; Germline alignment; Repertoire analysis

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

APA (6th Edition):

Chrysostomou, C. (2014). Addressing intrinsic challenges for next generation sequencing of immunoglobulin repertoires. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30450

Chicago Manual of Style (16th Edition):

Chrysostomou, Constantine. “Addressing intrinsic challenges for next generation sequencing of immunoglobulin repertoires.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed September 21, 2019. http://hdl.handle.net/2152/30450.

MLA Handbook (7th Edition):

Chrysostomou, Constantine. “Addressing intrinsic challenges for next generation sequencing of immunoglobulin repertoires.” 2014. Web. 21 Sep 2019.

Vancouver:

Chrysostomou C. Addressing intrinsic challenges for next generation sequencing of immunoglobulin repertoires. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2019 Sep 21]. Available from: http://hdl.handle.net/2152/30450.

Council of Science Editors:

Chrysostomou C. Addressing intrinsic challenges for next generation sequencing of immunoglobulin repertoires. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/30450

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