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You searched for +publisher:"University of Texas – Austin" +contributor:("Liu, Hung-wen"). Showing records 1 – 30 of 74 total matches.

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University of Texas – Austin

1. Gengler, Jon Peter. Biosynthesis of sulfur containing heterocycles in natural products.

Degree: MA, Biochemistry, 2016, University of Texas – Austin

 This thesis is a comprehensive review of the biosynthesis of sulfur containing heterocycles in natural metabolites. The review focuses on sulfur incorporation and cyclization of… (more)

Subjects/Keywords: Review; Sulfur; Heterocycle; Natural products; Disulfide; Thioether; Peptide; Thiazole; Thiazoline; Thiazolidine; Epipolythiodioxopiperazine; Gliotoxin; Dithiolopyrrolone; Holothin; Romidepsin; Lipoic acid; Tropodithietic acid; Thiotropocin; Asparagusic acid; Lantipeptide; Sactipeptide; Echinomycin; Nosiheptide; Amatoxin; Phallotoxin; Nereistoxin; Gerrardine; Malformin; Trabectedin; Penam; Thiamine; Luciferin; Dercitin; S1319; Violatinctamine; Cepham; Chuangxinmycin; 7-Hydroxy-5-hydroxymethyl-2H-benzo[1,4]thiazin-3-one; Cruciferous phytoalexins; Nasturlexin; Camalexin; Brassinin; Theindolin; Spirobrassinin; Cyclobrassinin; Thiosugar; Kotalanol; Ponkolanol; Salacinol; Salaprinol; Tagetitoxin; Albomycin; Lenthionine; 1,2,3,5-Tetrathiane-5,5-dioxide; Varacin; Lissoclibadin; Cassipoureamide; Caldariellaquinone; Leinamycin; Biotin; Thiolactomycin; Cysteine

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APA (6th Edition):

Gengler, J. P. (2016). Biosynthesis of sulfur containing heterocycles in natural products. (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46176

Chicago Manual of Style (16th Edition):

Gengler, Jon Peter. “Biosynthesis of sulfur containing heterocycles in natural products.” 2016. Masters Thesis, University of Texas – Austin. Accessed November 28, 2020. http://hdl.handle.net/2152/46176.

MLA Handbook (7th Edition):

Gengler, Jon Peter. “Biosynthesis of sulfur containing heterocycles in natural products.” 2016. Web. 28 Nov 2020.

Vancouver:

Gengler JP. Biosynthesis of sulfur containing heterocycles in natural products. [Internet] [Masters thesis]. University of Texas – Austin; 2016. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2152/46176.

Council of Science Editors:

Gengler JP. Biosynthesis of sulfur containing heterocycles in natural products. [Masters Thesis]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/46176


University of Texas – Austin

2. Kim, Nam Ho, 1975-. Mechanistic investigations of SpnF- and SpnL-catalyzed cyclizations in the biosynthesis of spinosyn A.

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

 Spinosyn A is a particularly interesting natural product due to its structural complexity and potent insecticidal activity. The biosynthetic pathway of spinosyn A is interesting… (more)

Subjects/Keywords: Spinosyn A; Cyclization; Cycloaddition; SpnF; SpnL; Mechanism; Diels-Alder; Rauhut-Currier; Kinetic isotope effect; Mechanism-based inhibitor

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APA (6th Edition):

Kim, Nam Ho, 1. (2013). Mechanistic investigations of SpnF- and SpnL-catalyzed cyclizations in the biosynthesis of spinosyn A. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/28735

Chicago Manual of Style (16th Edition):

Kim, Nam Ho, 1975-. “Mechanistic investigations of SpnF- and SpnL-catalyzed cyclizations in the biosynthesis of spinosyn A.” 2013. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://hdl.handle.net/2152/28735.

MLA Handbook (7th Edition):

Kim, Nam Ho, 1975-. “Mechanistic investigations of SpnF- and SpnL-catalyzed cyclizations in the biosynthesis of spinosyn A.” 2013. Web. 28 Nov 2020.

Vancouver:

Kim, Nam Ho 1. Mechanistic investigations of SpnF- and SpnL-catalyzed cyclizations in the biosynthesis of spinosyn A. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2152/28735.

Council of Science Editors:

Kim, Nam Ho 1. Mechanistic investigations of SpnF- and SpnL-catalyzed cyclizations in the biosynthesis of spinosyn A. [Doctoral Dissertation]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/28735


University of Texas – Austin

3. Choi, Sei Hyun. Synthetic approaches to investigate the chemical mechanism in the biosynthesis of natural products.

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

 The study of the biosynthetic logic of natural products has established itself to be one of the more exciting areas of research and have become… (more)

Subjects/Keywords: Natural product; Chemical mechanism; Organic synthesis; Spinosyn; Diels-Alder reaction; Rauhut-Currier reaction; Apiose; AXS; Desii; Radical SAM enzyme

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APA (6th Edition):

Choi, S. H. (2012). Synthetic approaches to investigate the chemical mechanism in the biosynthesis of natural products. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/26079

Chicago Manual of Style (16th Edition):

Choi, Sei Hyun. “Synthetic approaches to investigate the chemical mechanism in the biosynthesis of natural products.” 2012. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://hdl.handle.net/2152/26079.

MLA Handbook (7th Edition):

Choi, Sei Hyun. “Synthetic approaches to investigate the chemical mechanism in the biosynthesis of natural products.” 2012. Web. 28 Nov 2020.

Vancouver:

Choi SH. Synthetic approaches to investigate the chemical mechanism in the biosynthesis of natural products. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2012. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2152/26079.

Council of Science Editors:

Choi SH. Synthetic approaches to investigate the chemical mechanism in the biosynthesis of natural products. [Doctoral Dissertation]. University of Texas – Austin; 2012. Available from: http://hdl.handle.net/2152/26079


University of Texas – Austin

4. Isiorho, Eta Amauche. Structural characterization of post-PKS enzymes involved in spinosyn biosynthesis.

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

 Saccharopolyspora spinosa is a rare actinomycete that synthesizes the secondary metabolite spinosyn A, which is an active ingredient in several important commercial insecticides. Spinosyn aglycone… (more)

Subjects/Keywords: Biosynthesis; Spinosyn; Structural; X-ray; Polyketide; Cyclase; Glycosyltransferase

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APA (6th Edition):

Isiorho, E. A. (2014). Structural characterization of post-PKS enzymes involved in spinosyn biosynthesis. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/29246

Chicago Manual of Style (16th Edition):

Isiorho, Eta Amauche. “Structural characterization of post-PKS enzymes involved in spinosyn biosynthesis.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://hdl.handle.net/2152/29246.

MLA Handbook (7th Edition):

Isiorho, Eta Amauche. “Structural characterization of post-PKS enzymes involved in spinosyn biosynthesis.” 2014. Web. 28 Nov 2020.

Vancouver:

Isiorho EA. Structural characterization of post-PKS enzymes involved in spinosyn biosynthesis. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2152/29246.

Council of Science Editors:

Isiorho EA. Structural characterization of post-PKS enzymes involved in spinosyn biosynthesis. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/29246

5. Tao, Zhihua, 1977-. Poly(ADP-ribose) polymerase-1 : domain C structure, poly(ADP-ribosyl)ation sites and physiological functions.

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

 Poly(ADP-ribose) polymerase-1 (PARP-1) is an abundant nuclear protein that catalyzes the cleavage of NAD⁺ into nicotinamide and ADP-ribose moiety, the latter of which may be… (more)

Subjects/Keywords: Poly(ADP-ribose) polymerase-1; Nucleoproteins

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APA (6th Edition):

Tao, Zhihua, 1. (2008). Poly(ADP-ribose) polymerase-1 : domain C structure, poly(ADP-ribosyl)ation sites and physiological functions. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/17912

Chicago Manual of Style (16th Edition):

Tao, Zhihua, 1977-. “Poly(ADP-ribose) polymerase-1 : domain C structure, poly(ADP-ribosyl)ation sites and physiological functions.” 2008. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://hdl.handle.net/2152/17912.

MLA Handbook (7th Edition):

Tao, Zhihua, 1977-. “Poly(ADP-ribose) polymerase-1 : domain C structure, poly(ADP-ribosyl)ation sites and physiological functions.” 2008. Web. 28 Nov 2020.

Vancouver:

Tao, Zhihua 1. Poly(ADP-ribose) polymerase-1 : domain C structure, poly(ADP-ribosyl)ation sites and physiological functions. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2008. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2152/17912.

Council of Science Editors:

Tao, Zhihua 1. Poly(ADP-ribose) polymerase-1 : domain C structure, poly(ADP-ribosyl)ation sites and physiological functions. [Doctoral Dissertation]. University of Texas – Austin; 2008. Available from: http://hdl.handle.net/2152/17912

6. Zhou, Ying, 1977-. Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF).

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

 Poly(ADP-ribosyl)ation, a covalent modification of proteins catalyzed by poly(ADP-ribose) polymerases (PARPs), plays a crucial role in regulating DNA repair, DNA replication, and cell death. Poly(ADP-ribose)… (more)

Subjects/Keywords: DNA repair; Poly(ADP-ribosyl)ation; Poly(ADP-ribose) polymerases; Poly(ADP-ribose) Polymerase-1; Zinc fingers; PARP; DNA-binding protein; DNA-binding properties; Apoptosis

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APA (6th Edition):

Zhou, Ying, 1. (2009). Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF). (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/21906

Chicago Manual of Style (16th Edition):

Zhou, Ying, 1977-. “Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF).” 2009. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://hdl.handle.net/2152/21906.

MLA Handbook (7th Edition):

Zhou, Ying, 1977-. “Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF).” 2009. Web. 28 Nov 2020.

Vancouver:

Zhou, Ying 1. Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF). [Internet] [Doctoral dissertation]. University of Texas – Austin; 2009. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2152/21906.

Council of Science Editors:

Zhou, Ying 1. Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF). [Doctoral Dissertation]. University of Texas – Austin; 2009. Available from: http://hdl.handle.net/2152/21906

7. Kim, Hak Joong, 1974-. Investigation of the post-polyketide synthase (PKS) modifications during spinosyn A biosynthesis in Saccharopolyspora spinosa.

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

 Diverse biological activities of polyketide natural products are often associated with specific structural motifs, biosynthetically introduced after construction of the polyketide core. Therefore, investigation of… (more)

Subjects/Keywords: Polyketide; Biosynthesis; Spinosyn; Methyltransferase; Diels-Alderase; Rauhut-Currier reaction; Intramolecular C-C bond formation; Kinetics; Enzyme mechanism

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APA (6th Edition):

Kim, Hak Joong, 1. (2010). Investigation of the post-polyketide synthase (PKS) modifications during spinosyn A biosynthesis in Saccharopolyspora spinosa. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/22143

Chicago Manual of Style (16th Edition):

Kim, Hak Joong, 1974-. “Investigation of the post-polyketide synthase (PKS) modifications during spinosyn A biosynthesis in Saccharopolyspora spinosa.” 2010. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://hdl.handle.net/2152/22143.

MLA Handbook (7th Edition):

Kim, Hak Joong, 1974-. “Investigation of the post-polyketide synthase (PKS) modifications during spinosyn A biosynthesis in Saccharopolyspora spinosa.” 2010. Web. 28 Nov 2020.

Vancouver:

Kim, Hak Joong 1. Investigation of the post-polyketide synthase (PKS) modifications during spinosyn A biosynthesis in Saccharopolyspora spinosa. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2010. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2152/22143.

Council of Science Editors:

Kim, Hak Joong 1. Investigation of the post-polyketide synthase (PKS) modifications during spinosyn A biosynthesis in Saccharopolyspora spinosa. [Doctoral Dissertation]. University of Texas – Austin; 2010. Available from: http://hdl.handle.net/2152/22143

8. Yu, Wei-luen Allen. Studies of the biosynthesis of the nitro sugar D-kijanose and the function of the glycosyltransferase helper proteins in glycosylation of macrolide antibiotics.

Degree: PhD, Molecular Biology, 2007, University of Texas – Austin

 The appended sugar residues of many natural products from Actinomyces are important for their biological activities. Many of these unusual sugar biosynthetic gene clusters have… (more)

Subjects/Keywords: Biosynthetic pathways; D-kijanose; Glycosyitransferase; Glycosylation; Macrolide antibiotics

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APA (6th Edition):

Yu, W. A. (2007). Studies of the biosynthesis of the nitro sugar D-kijanose and the function of the glycosyltransferase helper proteins in glycosylation of macrolide antibiotics. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/24376

Chicago Manual of Style (16th Edition):

Yu, Wei-luen Allen. “Studies of the biosynthesis of the nitro sugar D-kijanose and the function of the glycosyltransferase helper proteins in glycosylation of macrolide antibiotics.” 2007. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://hdl.handle.net/2152/24376.

MLA Handbook (7th Edition):

Yu, Wei-luen Allen. “Studies of the biosynthesis of the nitro sugar D-kijanose and the function of the glycosyltransferase helper proteins in glycosylation of macrolide antibiotics.” 2007. Web. 28 Nov 2020.

Vancouver:

Yu WA. Studies of the biosynthesis of the nitro sugar D-kijanose and the function of the glycosyltransferase helper proteins in glycosylation of macrolide antibiotics. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2007. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2152/24376.

Council of Science Editors:

Yu WA. Studies of the biosynthesis of the nitro sugar D-kijanose and the function of the glycosyltransferase helper proteins in glycosylation of macrolide antibiotics. [Doctoral Dissertation]. University of Texas – Austin; 2007. Available from: http://hdl.handle.net/2152/24376


University of Texas – Austin

9. 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 November 28, 2020. 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. 28 Nov 2020.

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 2020 Nov 28]. 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

10. -7981-5709. Rhodium(I)-catalyzed C–C bond activation : decarbonylation of α,β-acetylenic ketones: Rhodium(I)-catalyzed C–C bond activation : decarbonylation of [alpha], [beta]-acetylenic ketones.

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

 Transition metal-catalyzed carbon–carbon (C–C) bond activation is a useful way to construct organic molecules that could be difficult or impossible to achieve under traditional synthetic… (more)

Subjects/Keywords: Carbon-alkyne activation; Decarbonylation; Ynone

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APA (6th Edition):

-7981-5709. (2016). Rhodium(I)-catalyzed C–C bond activation : decarbonylation of α,β-acetylenic ketones: Rhodium(I)-catalyzed C–C bond activation : decarbonylation of [alpha], [beta]-acetylenic ketones. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/40932

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

Chicago Manual of Style (16th Edition):

-7981-5709. “Rhodium(I)-catalyzed C–C bond activation : decarbonylation of α,β-acetylenic ketones: Rhodium(I)-catalyzed C–C bond activation : decarbonylation of [alpha], [beta]-acetylenic ketones.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://hdl.handle.net/2152/40932.

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

MLA Handbook (7th Edition):

-7981-5709. “Rhodium(I)-catalyzed C–C bond activation : decarbonylation of α,β-acetylenic ketones: Rhodium(I)-catalyzed C–C bond activation : decarbonylation of [alpha], [beta]-acetylenic ketones.” 2016. Web. 28 Nov 2020.

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

Vancouver:

-7981-5709. Rhodium(I)-catalyzed C–C bond activation : decarbonylation of α,β-acetylenic ketones: Rhodium(I)-catalyzed C–C bond activation : decarbonylation of [alpha], [beta]-acetylenic ketones. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2152/40932.

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

Council of Science Editors:

-7981-5709. Rhodium(I)-catalyzed C–C bond activation : decarbonylation of α,β-acetylenic ketones: Rhodium(I)-catalyzed C–C bond activation : decarbonylation of [alpha], [beta]-acetylenic ketones. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/40932

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


University of Texas – Austin

11. 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 November 28, 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. 28 Nov 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 Nov 28]. 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

12. Luong, Tom Tuan. Development of transition metal catalyzed carbon-carbon bond forming reactions with abundant or scarce chemicals.

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

 The development of more efficient carbon-carbon bond transformation is of great significance. One of the more common approaches to forging carbon-carbon bonds is the addition… (more)

Subjects/Keywords: Transfer hydrogenation

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APA (6th Edition):

Luong, T. T. (2017). Development of transition metal catalyzed carbon-carbon bond forming reactions with abundant or scarce chemicals. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/61785

Chicago Manual of Style (16th Edition):

Luong, Tom Tuan. “Development of transition metal catalyzed carbon-carbon bond forming reactions with abundant or scarce chemicals.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://hdl.handle.net/2152/61785.

MLA Handbook (7th Edition):

Luong, Tom Tuan. “Development of transition metal catalyzed carbon-carbon bond forming reactions with abundant or scarce chemicals.” 2017. Web. 28 Nov 2020.

Vancouver:

Luong TT. Development of transition metal catalyzed carbon-carbon bond forming reactions with abundant or scarce chemicals. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2152/61785.

Council of Science Editors:

Luong TT. Development of transition metal catalyzed carbon-carbon bond forming reactions with abundant or scarce chemicals. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/61785


University of Texas – Austin

13. Nelson, Andrew Timothy. Synthesis, SAR library, and chemical biology probes of PAHSAs, a family of natural product lipids with anti-diabetic activity.

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

 Nearly one in ten Americans has type 2 diabetes mellitus (T2DM), a major source of morbidity, mortality, and healthcare costs. Most patients with diabetes are… (more)

Subjects/Keywords: FAHFA; PAHSA; Diabetes

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APA (6th Edition):

Nelson, A. T. (2018). Synthesis, SAR library, and chemical biology probes of PAHSAs, a family of natural product lipids with anti-diabetic activity. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/69042

Chicago Manual of Style (16th Edition):

Nelson, Andrew Timothy. “Synthesis, SAR library, and chemical biology probes of PAHSAs, a family of natural product lipids with anti-diabetic activity.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://hdl.handle.net/2152/69042.

MLA Handbook (7th Edition):

Nelson, Andrew Timothy. “Synthesis, SAR library, and chemical biology probes of PAHSAs, a family of natural product lipids with anti-diabetic activity.” 2018. Web. 28 Nov 2020.

Vancouver:

Nelson AT. Synthesis, SAR library, and chemical biology probes of PAHSAs, a family of natural product lipids with anti-diabetic activity. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2152/69042.

Council of Science Editors:

Nelson AT. Synthesis, SAR library, and chemical biology probes of PAHSAs, a family of natural product lipids with anti-diabetic activity. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/69042


University of Texas – Austin

14. -3473-3494. Total syntheses of the regenerative natural products vinaxanthone, xanthofulvin, and eupalinilide E.

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

 The fungal metabolites vinaxanthone and xanthofulvin possess the remarkable ability to restore motor function in animal models of complete spinal cord transection making them the… (more)

Subjects/Keywords: Regenerative natural products; Vinaxanthone; Xanthofulvin; Eupalinilide E

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APA (6th Edition):

-3473-3494. (2015). Total syntheses of the regenerative natural products vinaxanthone, xanthofulvin, and eupalinilide E. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30456

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-3473-3494. “Total syntheses of the regenerative natural products vinaxanthone, xanthofulvin, and eupalinilide E.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://hdl.handle.net/2152/30456.

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Author name may be incomplete

MLA Handbook (7th Edition):

-3473-3494. “Total syntheses of the regenerative natural products vinaxanthone, xanthofulvin, and eupalinilide E.” 2015. Web. 28 Nov 2020.

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Author name may be incomplete

Vancouver:

-3473-3494. Total syntheses of the regenerative natural products vinaxanthone, xanthofulvin, and eupalinilide E. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2152/30456.

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Author name may be incomplete

Council of Science Editors:

-3473-3494. Total syntheses of the regenerative natural products vinaxanthone, xanthofulvin, and eupalinilide E. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/30456

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Author name may be incomplete


University of Texas – Austin

15. Maher, Michael Joseph. Next generation materials for block copolymer lithography.

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

 The electronics industry is a trillion dollar industry that has drastically changed everyday life. Advances in lithography have enabled manufacturers to continually shrink the dimensions… (more)

Subjects/Keywords: Block copolymers; Directed self-assembly; Lithography

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APA (6th Edition):

Maher, M. J. (2018). Next generation materials for block copolymer lithography. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68906

Chicago Manual of Style (16th Edition):

Maher, Michael Joseph. “Next generation materials for block copolymer lithography.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://hdl.handle.net/2152/68906.

MLA Handbook (7th Edition):

Maher, Michael Joseph. “Next generation materials for block copolymer lithography.” 2018. Web. 28 Nov 2020.

Vancouver:

Maher MJ. Next generation materials for block copolymer lithography. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2152/68906.

Council of Science Editors:

Maher MJ. Next generation materials for block copolymer lithography. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/68906


University of Texas – Austin

16. Myler, Logan Ross. Single-molecule studies reveal mechanisms of human DNA double-strand break repair.

Degree: PhD, Cell and molecular biology, 2018, University of Texas – Austin

 DNA damage is ubiquitous to all organisms and very complex pathways have evolved to recognize and repair these lesions. The most deleterious DNA damages are… (more)

Subjects/Keywords: DNA; Double-strand break; MRN; Exo1; Resection; Resectosome; Homologous recombination

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APA (6th Edition):

Myler, L. R. (2018). Single-molecule studies reveal mechanisms of human DNA double-strand break repair. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/9477

Chicago Manual of Style (16th Edition):

Myler, Logan Ross. “Single-molecule studies reveal mechanisms of human DNA double-strand break repair.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://dx.doi.org/10.26153/tsw/9477.

MLA Handbook (7th Edition):

Myler, Logan Ross. “Single-molecule studies reveal mechanisms of human DNA double-strand break repair.” 2018. Web. 28 Nov 2020.

Vancouver:

Myler LR. Single-molecule studies reveal mechanisms of human DNA double-strand break repair. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2020 Nov 28]. Available from: http://dx.doi.org/10.26153/tsw/9477.

Council of Science Editors:

Myler LR. Single-molecule studies reveal mechanisms of human DNA double-strand break repair. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://dx.doi.org/10.26153/tsw/9477


University of Texas – Austin

17. -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 November 28, 2020. 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. 28 Nov 2020.

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 2020 Nov 28]. 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

18. -8750-5428. Rhodium porphyrin alkylations with ammonium and quinolinium salts and cyclic ether formation via a palladium catalyzed dehydrogenative annulation.

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

 The formation and study of metal–carbon σ-bonds can help unveil unique reactivities of organometallic complexes and provide support for further catalytic transformations. Rhodium porphyrins have… (more)

Subjects/Keywords: Palladium; Directing group; Catalysis; Rhodium porphyrin; Alkylation; Cyclic ether synthesis

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APA (6th Edition):

-8750-5428. (2016). Rhodium porphyrin alkylations with ammonium and quinolinium salts and cyclic ether formation via a palladium catalyzed dehydrogenative annulation. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/39652

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-8750-5428. “Rhodium porphyrin alkylations with ammonium and quinolinium salts and cyclic ether formation via a palladium catalyzed dehydrogenative annulation.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://hdl.handle.net/2152/39652.

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Author name may be incomplete

MLA Handbook (7th Edition):

-8750-5428. “Rhodium porphyrin alkylations with ammonium and quinolinium salts and cyclic ether formation via a palladium catalyzed dehydrogenative annulation.” 2016. Web. 28 Nov 2020.

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

Vancouver:

-8750-5428. Rhodium porphyrin alkylations with ammonium and quinolinium salts and cyclic ether formation via a palladium catalyzed dehydrogenative annulation. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2152/39652.

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

Council of Science Editors:

-8750-5428. Rhodium porphyrin alkylations with ammonium and quinolinium salts and cyclic ether formation via a palladium catalyzed dehydrogenative annulation. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/39652

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Author name may be incomplete


University of Texas – Austin

19. -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 November 28, 2020. 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. 28 Nov 2020.

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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 2020 Nov 28]. 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

20. Lin, Geng-Min. Unusual carbohydrate biosynthesis : studies of the flavin-dependent isomerase UGM, the radical S-adenosyl-L-methionine enzyme DesII, and the biosynthesis of herbicidins.

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

 Bacteria produce a great variety of unusual carbohydrates that are often found as parts of their cell surfaces or secondary metabolites. These components are crucial… (more)

Subjects/Keywords: Unusual carbohydrate; Biosynthesis; UDP-galactopyranose mutase; DesII; Radical SAM enzyme; Herbicidin

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APA (6th Edition):

Lin, G. (2017). Unusual carbohydrate biosynthesis : studies of the flavin-dependent isomerase UGM, the radical S-adenosyl-L-methionine enzyme DesII, and the biosynthesis of herbicidins. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/5870

Chicago Manual of Style (16th Edition):

Lin, Geng-Min. “Unusual carbohydrate biosynthesis : studies of the flavin-dependent isomerase UGM, the radical S-adenosyl-L-methionine enzyme DesII, and the biosynthesis of herbicidins.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://dx.doi.org/10.26153/tsw/5870.

MLA Handbook (7th Edition):

Lin, Geng-Min. “Unusual carbohydrate biosynthesis : studies of the flavin-dependent isomerase UGM, the radical S-adenosyl-L-methionine enzyme DesII, and the biosynthesis of herbicidins.” 2017. Web. 28 Nov 2020.

Vancouver:

Lin G. Unusual carbohydrate biosynthesis : studies of the flavin-dependent isomerase UGM, the radical S-adenosyl-L-methionine enzyme DesII, and the biosynthesis of herbicidins. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2020 Nov 28]. Available from: http://dx.doi.org/10.26153/tsw/5870.

Council of Science Editors:

Lin G. Unusual carbohydrate biosynthesis : studies of the flavin-dependent isomerase UGM, the radical S-adenosyl-L-methionine enzyme DesII, and the biosynthesis of herbicidins. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://dx.doi.org/10.26153/tsw/5870


University of Texas – Austin

21. -1902-3184. Transition metal catalyzed redox triggered C–C bond forming reactions of alcohols via transfer hydrogenation.

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

 Carbonyl addition is one of the fundamental reactions forming C–C bonds in organic chemistry to construct structurally complex organic molecules, in particular natural products, from… (more)

Subjects/Keywords: C–C bond forming reaction; Transition metal catalysis; Transfer hydrogenation

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APA (6th Edition):

-1902-3184. (2016). Transition metal catalyzed redox triggered C–C bond forming reactions of alcohols via transfer hydrogenation. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46996

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-1902-3184. “Transition metal catalyzed redox triggered C–C bond forming reactions of alcohols via transfer hydrogenation.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://hdl.handle.net/2152/46996.

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Author name may be incomplete

MLA Handbook (7th Edition):

-1902-3184. “Transition metal catalyzed redox triggered C–C bond forming reactions of alcohols via transfer hydrogenation.” 2016. Web. 28 Nov 2020.

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

Vancouver:

-1902-3184. Transition metal catalyzed redox triggered C–C bond forming reactions of alcohols via transfer hydrogenation. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2152/46996.

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

Council of Science Editors:

-1902-3184. Transition metal catalyzed redox triggered C–C bond forming reactions of alcohols via transfer hydrogenation. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/46996

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Author name may be incomplete


University of Texas – Austin

22. Erwin, Kaci Leigh. Investigation of the ring-cleaving dioxygenase and hydratase-aldolase reactions in the Mycobacterium vanbaalenii PYR-1 catabolic pathways.

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

 Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous environmental pollutants made of fused aromatic rings. The improper disposal of petrochemicals is a major source of PAHs in… (more)

Subjects/Keywords: Polycyclic aromatic hydrocarbons; Mycobacterium vanbaalenii PYR-1; PAH degradation; Ring-cleaving dioxygenase; Phenanthrene catabolism; Naphthalene catabolism

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APA (6th Edition):

Erwin, K. L. (2018). Investigation of the ring-cleaving dioxygenase and hydratase-aldolase reactions in the Mycobacterium vanbaalenii PYR-1 catabolic pathways. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68925

Chicago Manual of Style (16th Edition):

Erwin, Kaci Leigh. “Investigation of the ring-cleaving dioxygenase and hydratase-aldolase reactions in the Mycobacterium vanbaalenii PYR-1 catabolic pathways.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://hdl.handle.net/2152/68925.

MLA Handbook (7th Edition):

Erwin, Kaci Leigh. “Investigation of the ring-cleaving dioxygenase and hydratase-aldolase reactions in the Mycobacterium vanbaalenii PYR-1 catabolic pathways.” 2018. Web. 28 Nov 2020.

Vancouver:

Erwin KL. Investigation of the ring-cleaving dioxygenase and hydratase-aldolase reactions in the Mycobacterium vanbaalenii PYR-1 catabolic pathways. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2152/68925.

Council of Science Editors:

Erwin KL. Investigation of the ring-cleaving dioxygenase and hydratase-aldolase reactions in the Mycobacterium vanbaalenii PYR-1 catabolic pathways. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/68925


University of Texas – Austin

23. -2348-5939. Synthesis of aza-spirocyclic dienones and their application toward natural product synthesis and synthesis and evaluation of anticancer tetracyclic indole containing compounds: Synthesis and evaluation of anticancer tetracyclic indole containing compounds.

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

 A novel route to access the aza-spirocyclic cross-conjugated dienone motif was developed utilizing an intramolecular phenolic C-alkylation and Suzuki coupling to form the key quaternary… (more)

Subjects/Keywords: Aza-dienone; Indole; Actinophyllic acid; Anticancer

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APA (6th Edition):

-2348-5939. (2018). Synthesis of aza-spirocyclic dienones and their application toward natural product synthesis and synthesis and evaluation of anticancer tetracyclic indole containing compounds: Synthesis and evaluation of anticancer tetracyclic indole containing compounds. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68761

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-2348-5939. “Synthesis of aza-spirocyclic dienones and their application toward natural product synthesis and synthesis and evaluation of anticancer tetracyclic indole containing compounds: Synthesis and evaluation of anticancer tetracyclic indole containing compounds.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://hdl.handle.net/2152/68761.

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Author name may be incomplete

MLA Handbook (7th Edition):

-2348-5939. “Synthesis of aza-spirocyclic dienones and their application toward natural product synthesis and synthesis and evaluation of anticancer tetracyclic indole containing compounds: Synthesis and evaluation of anticancer tetracyclic indole containing compounds.” 2018. Web. 28 Nov 2020.

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Author name may be incomplete

Vancouver:

-2348-5939. Synthesis of aza-spirocyclic dienones and their application toward natural product synthesis and synthesis and evaluation of anticancer tetracyclic indole containing compounds: Synthesis and evaluation of anticancer tetracyclic indole containing compounds. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2152/68761.

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Author name may be incomplete

Council of Science Editors:

-2348-5939. Synthesis of aza-spirocyclic dienones and their application toward natural product synthesis and synthesis and evaluation of anticancer tetracyclic indole containing compounds: Synthesis and evaluation of anticancer tetracyclic indole containing compounds. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/68761

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Author name may be incomplete


University of Texas – Austin

24. -2285-9214. Growth-regulated Hsp70 phosphorylation regulates stress responses and prion maintenance.

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

 Maintenance of protein homeostasis in eukaryotes during normal growth and stress conditions requires the functions of Hsp70 chaperones and associated co-chaperones. Here we investigate an… (more)

Subjects/Keywords: Hsp70; Phosphorylation; Protein homeostasis; Protein aggregation; Hsp104; Yeast; Prion

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APA (6th Edition):

-2285-9214. (2020). Growth-regulated Hsp70 phosphorylation regulates stress responses and prion maintenance. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/8995

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-2285-9214. “Growth-regulated Hsp70 phosphorylation regulates stress responses and prion maintenance.” 2020. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://dx.doi.org/10.26153/tsw/8995.

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MLA Handbook (7th Edition):

-2285-9214. “Growth-regulated Hsp70 phosphorylation regulates stress responses and prion maintenance.” 2020. Web. 28 Nov 2020.

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

Vancouver:

-2285-9214. Growth-regulated Hsp70 phosphorylation regulates stress responses and prion maintenance. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2020. [cited 2020 Nov 28]. Available from: http://dx.doi.org/10.26153/tsw/8995.

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

Council of Science Editors:

-2285-9214. Growth-regulated Hsp70 phosphorylation regulates stress responses and prion maintenance. [Doctoral Dissertation]. University of Texas – Austin; 2020. Available from: http://dx.doi.org/10.26153/tsw/8995

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Author name may be incomplete


University of Texas – Austin

25. Kim, Seung Wook, Ph. D. Amphiphilic [pi]-allyliridium catalyzed nucleophilic and electrophilic allylation.

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

 Transition metal-catalyzed allylic substitution has emerged as a powerful method for stereoselective C-N bond formation. Chiral iridium-phosphoramidite complexes have proven especially effective as catalysts for… (more)

Subjects/Keywords: Transition metal; Allylic substitution; Iridium

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APA (6th Edition):

Kim, Seung Wook, P. D. (2020). Amphiphilic [pi]-allyliridium catalyzed nucleophilic and electrophilic allylation. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/9154

Chicago Manual of Style (16th Edition):

Kim, Seung Wook, Ph D. “Amphiphilic [pi]-allyliridium catalyzed nucleophilic and electrophilic allylation.” 2020. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://dx.doi.org/10.26153/tsw/9154.

MLA Handbook (7th Edition):

Kim, Seung Wook, Ph D. “Amphiphilic [pi]-allyliridium catalyzed nucleophilic and electrophilic allylation.” 2020. Web. 28 Nov 2020.

Vancouver:

Kim, Seung Wook PD. Amphiphilic [pi]-allyliridium catalyzed nucleophilic and electrophilic allylation. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2020. [cited 2020 Nov 28]. Available from: http://dx.doi.org/10.26153/tsw/9154.

Council of Science Editors:

Kim, Seung Wook PD. Amphiphilic [pi]-allyliridium catalyzed nucleophilic and electrophilic allylation. [Doctoral Dissertation]. University of Texas – Austin; 2020. Available from: http://dx.doi.org/10.26153/tsw/9154


University of Texas – Austin

26. -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 November 28, 2020. http://hdl.handle.net/2152/68375.

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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. 28 Nov 2020.

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 2020 Nov 28]. 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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University of Texas – Austin

27. Jo, Hyun Hwa. Optical chirality sensing ensembles : mechanistic studies and applications in synthetic methodology development.

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

 In the pharmaceutical industry, the development of molecular or chemical sensors for an analyte of interest and the determination of the enantiomeric purity of chiral… (more)

Subjects/Keywords: Optical ee sensing; High-throughput ee sensing; Enantiomeric excess; Enantiomeric excess analysis; ee analysis; ee screening; Chirality sensing; Multi-component assembly reaction; Chiral ketones; Synthetic methodology

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

APA (6th Edition):

Jo, H. H. (2015). Optical chirality sensing ensembles : mechanistic studies and applications in synthetic methodology development. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46977

Chicago Manual of Style (16th Edition):

Jo, Hyun Hwa. “Optical chirality sensing ensembles : mechanistic studies and applications in synthetic methodology development.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://hdl.handle.net/2152/46977.

MLA Handbook (7th Edition):

Jo, Hyun Hwa. “Optical chirality sensing ensembles : mechanistic studies and applications in synthetic methodology development.” 2015. Web. 28 Nov 2020.

Vancouver:

Jo HH. Optical chirality sensing ensembles : mechanistic studies and applications in synthetic methodology development. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2152/46977.

Council of Science Editors:

Jo HH. Optical chirality sensing ensembles : mechanistic studies and applications in synthetic methodology development. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46977


University of Texas – Austin

28. Hassan, Abbas. Development of new transition metal catalyzed C-C bond forming reactions and their application toward natural product synthesis.

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

 In Michael J. Krische research group we are developing new transition metal catalyzed Carbon-Carbon (C-C) forming reactions focusing on atom economy and byproduct free, environmental… (more)

Subjects/Keywords: Hydrogenation C-C bond formation; Transfer hydrogenation C-C bond formation; Total synthesis; Roxaticin; Aldol reaction; Enantioselective vinylogous aldol-Reformatsky reaction; Enantioselective Grignard Nozaki-Hiyama Methallylation

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

APA (6th Edition):

Hassan, A. (2011). Development of new transition metal catalyzed C-C bond forming reactions and their application toward natural product synthesis. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/ETD-UT-2011-12-4837

Chicago Manual of Style (16th Edition):

Hassan, Abbas. “Development of new transition metal catalyzed C-C bond forming reactions and their application toward natural product synthesis.” 2011. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://hdl.handle.net/2152/ETD-UT-2011-12-4837.

MLA Handbook (7th Edition):

Hassan, Abbas. “Development of new transition metal catalyzed C-C bond forming reactions and their application toward natural product synthesis.” 2011. Web. 28 Nov 2020.

Vancouver:

Hassan A. Development of new transition metal catalyzed C-C bond forming reactions and their application toward natural product synthesis. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2011. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2152/ETD-UT-2011-12-4837.

Council of Science Editors:

Hassan A. Development of new transition metal catalyzed C-C bond forming reactions and their application toward natural product synthesis. [Doctoral Dissertation]. University of Texas – Austin; 2011. Available from: http://hdl.handle.net/2152/ETD-UT-2011-12-4837


University of Texas – Austin

29. Vasicek, Lisa Anne. Enhanced protein characterization through selective derivatization and electrospray ionization tandem mass spectrometry.

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

 There continue to be great strides in the field of proteomics but as samples become more complex, the ability to increase sequence coverage and confidence… (more)

Subjects/Keywords: Mass spectrometry; Selective derivatization; Proteomics

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

APA (6th Edition):

Vasicek, L. A. (2011). Enhanced protein characterization through selective derivatization and electrospray ionization tandem mass spectrometry. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/ETD-UT-2011-08-4198

Chicago Manual of Style (16th Edition):

Vasicek, Lisa Anne. “Enhanced protein characterization through selective derivatization and electrospray ionization tandem mass spectrometry.” 2011. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://hdl.handle.net/2152/ETD-UT-2011-08-4198.

MLA Handbook (7th Edition):

Vasicek, Lisa Anne. “Enhanced protein characterization through selective derivatization and electrospray ionization tandem mass spectrometry.” 2011. Web. 28 Nov 2020.

Vancouver:

Vasicek LA. Enhanced protein characterization through selective derivatization and electrospray ionization tandem mass spectrometry. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2011. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2152/ETD-UT-2011-08-4198.

Council of Science Editors:

Vasicek LA. Enhanced protein characterization through selective derivatization and electrospray ionization tandem mass spectrometry. [Doctoral Dissertation]. University of Texas – Austin; 2011. Available from: http://hdl.handle.net/2152/ETD-UT-2011-08-4198


University of Texas – Austin

30. -0166-1890. Transition metal-catalyzed transfer hydrogenative C-C bond formation : from methodology development to bryostatin analogue synthesis: Transition metal-catalyzed transfer hydrogenative carbon-carbon bond formation : from methodology development to bryostatin analogue synthesis.

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

 One of the more formidable challenges of organic synthesis remains the efficient construction of C-C bonds. A generally used strategy for carrying out such transformations… (more)

Subjects/Keywords: Transition-metal catalysis; Bryostatin analogue synthesis

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

APA (6th Edition):

-0166-1890. (2016). Transition metal-catalyzed transfer hydrogenative C-C bond formation : from methodology development to bryostatin analogue synthesis: Transition metal-catalyzed transfer hydrogenative carbon-carbon bond formation : from methodology development to bryostatin analogue synthesis. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/41729

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

Chicago Manual of Style (16th Edition):

-0166-1890. “Transition metal-catalyzed transfer hydrogenative C-C bond formation : from methodology development to bryostatin analogue synthesis: Transition metal-catalyzed transfer hydrogenative carbon-carbon bond formation : from methodology development to bryostatin analogue synthesis.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed November 28, 2020. http://hdl.handle.net/2152/41729.

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

MLA Handbook (7th Edition):

-0166-1890. “Transition metal-catalyzed transfer hydrogenative C-C bond formation : from methodology development to bryostatin analogue synthesis: Transition metal-catalyzed transfer hydrogenative carbon-carbon bond formation : from methodology development to bryostatin analogue synthesis.” 2016. Web. 28 Nov 2020.

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

Vancouver:

-0166-1890. Transition metal-catalyzed transfer hydrogenative C-C bond formation : from methodology development to bryostatin analogue synthesis: Transition metal-catalyzed transfer hydrogenative carbon-carbon bond formation : from methodology development to bryostatin analogue synthesis. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2152/41729.

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

Council of Science Editors:

-0166-1890. Transition metal-catalyzed transfer hydrogenative C-C bond formation : from methodology development to bryostatin analogue synthesis: Transition metal-catalyzed transfer hydrogenative carbon-carbon bond formation : from methodology development to bryostatin analogue synthesis. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/41729

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

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