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You searched for +publisher:"University of Illinois – Urbana-Champaign" +contributor:("van der Donk, Wilfred A."). Showing records 1 – 30 of 69 total matches.

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University of Illinois – Urbana-Champaign

1. Shea, Lindsey. Use of solution-state nuclear magnetic resonance spectroscopy to determine the structures of medicinally relevant peptides and proteins.

Degree: MS, 0335, 2012, University of Illinois – Urbana-Champaign

 The research described herein details various studies with solution-state nuclear magnetic resonance (NMR) spectroscopy to aid in the elucidation of structures of various medicinally relevant… (more)

Subjects/Keywords: nuclear magnetic resonance (NMR)spectroscopy; Lantibiotics; Lantipeptides; immunity; phosphite dehydrogenase; prochlorosin; cytolysin; NisI

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APA (6th Edition):

Shea, L. (2012). Use of solution-state nuclear magnetic resonance spectroscopy to determine the structures of medicinally relevant peptides and proteins. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/34455

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

Chicago Manual of Style (16th Edition):

Shea, Lindsey. “Use of solution-state nuclear magnetic resonance spectroscopy to determine the structures of medicinally relevant peptides and proteins.” 2012. Thesis, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/34455.

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

MLA Handbook (7th Edition):

Shea, Lindsey. “Use of solution-state nuclear magnetic resonance spectroscopy to determine the structures of medicinally relevant peptides and proteins.” 2012. Web. 15 Feb 2019.

Vancouver:

Shea L. Use of solution-state nuclear magnetic resonance spectroscopy to determine the structures of medicinally relevant peptides and proteins. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/34455.

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

Council of Science Editors:

Shea L. Use of solution-state nuclear magnetic resonance spectroscopy to determine the structures of medicinally relevant peptides and proteins. [Thesis]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/34455

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

2. Koh, Tong Hee. Studies towards understanding the function of LanCL1.

Degree: MS, 0318, 2012, University of Illinois – Urbana-Champaign

 LanC-like protein 1 (LanCL1) is a eukaryotic homolog of bacterial protein LanC. Unlike the well studied LanC proteins, the functions of LanC-like proteins are yet… (more)

Subjects/Keywords: LanCL1;

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APA (6th Edition):

Koh, T. H. (2012). Studies towards understanding the function of LanCL1. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/31101

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

Chicago Manual of Style (16th Edition):

Koh, Tong Hee. “Studies towards understanding the function of LanCL1.” 2012. Thesis, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/31101.

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

MLA Handbook (7th Edition):

Koh, Tong Hee. “Studies towards understanding the function of LanCL1.” 2012. Web. 15 Feb 2019.

Vancouver:

Koh TH. Studies towards understanding the function of LanCL1. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/31101.

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

Council of Science Editors:

Koh TH. Studies towards understanding the function of LanCL1. [Thesis]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/31101

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


University of Illinois – Urbana-Champaign

3. Wichelecki, Daniel. Functional and physiological discovery in the mannonate dehydratase subgroup of the enolase superfamily.

Degree: PhD, 0318, 2015, University of Illinois – Urbana-Champaign

 In the current post-genomic world, the exponential amassing of protein sequences is overwhelming the scientific community’s ability to experimentally assign each protein’s function. The use… (more)

Subjects/Keywords: Enzyme Function Initiative; enzyme; D-mannonate; L-gulonate; L-idonate; D-gluconate; mannonate dehydratase; gluconate dehydratase; Reverse Thymidylate Synthase (rTS); Enolase Superfamily Member 1 (ENOSF1); functional discovery; physiological discovery; enzyme evolution; Caulobacter; Salmonella; Chromohalobacter; enolase superfamily

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APA (6th Edition):

Wichelecki, D. (2015). Functional and physiological discovery in the mannonate dehydratase subgroup of the enolase superfamily. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/73007

Chicago Manual of Style (16th Edition):

Wichelecki, Daniel. “Functional and physiological discovery in the mannonate dehydratase subgroup of the enolase superfamily.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/73007.

MLA Handbook (7th Edition):

Wichelecki, Daniel. “Functional and physiological discovery in the mannonate dehydratase subgroup of the enolase superfamily.” 2015. Web. 15 Feb 2019.

Vancouver:

Wichelecki D. Functional and physiological discovery in the mannonate dehydratase subgroup of the enolase superfamily. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/73007.

Council of Science Editors:

Wichelecki D. Functional and physiological discovery in the mannonate dehydratase subgroup of the enolase superfamily. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/73007


University of Illinois – Urbana-Champaign

4. Peck, Spencer. Mechanistic investigations of enzymes in phosphonate metabolism.

Degree: PhD, 0335, 2015, University of Illinois – Urbana-Champaign

 Synthetic and naturally-occurring phosphonates have found widespread use in both agriculture and medicine. A program at the Institute for Genomic Biology at the University of… (more)

Subjects/Keywords: Phosphonate biosynthesis; enzymology; non-heme iron-dependent enzyme; 2-Hydroxyethylphosphonate dioxygenase (HEPD); methylphosphonate synthase (MPnS)

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APA (6th Edition):

Peck, S. (2015). Mechanistic investigations of enzymes in phosphonate metabolism. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/73062

Chicago Manual of Style (16th Edition):

Peck, Spencer. “Mechanistic investigations of enzymes in phosphonate metabolism.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/73062.

MLA Handbook (7th Edition):

Peck, Spencer. “Mechanistic investigations of enzymes in phosphonate metabolism.” 2015. Web. 15 Feb 2019.

Vancouver:

Peck S. Mechanistic investigations of enzymes in phosphonate metabolism. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/73062.

Council of Science Editors:

Peck S. Mechanistic investigations of enzymes in phosphonate metabolism. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/73062


University of Illinois – Urbana-Champaign

5. Zeng, Min. Investigations into the roles and molecular mechanisms of LanC-like proteins.

Degree: PhD, Cell and Developmental Biology, 2015, University of Illinois – Urbana-Champaign

 Lanthipeptides are a family of ribosomally synthesized and posttranslationally modified natural products defined by the characteristic thioether crosslinks lanthionine and methyllanthionine. Among the various biological… (more)

Subjects/Keywords: Lanthionine; Akt; lanthionine synthetase C–like 2 (LanCL2)

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APA (6th Edition):

Zeng, M. (2015). Investigations into the roles and molecular mechanisms of LanC-like proteins. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/78713

Chicago Manual of Style (16th Edition):

Zeng, Min. “Investigations into the roles and molecular mechanisms of LanC-like proteins.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/78713.

MLA Handbook (7th Edition):

Zeng, Min. “Investigations into the roles and molecular mechanisms of LanC-like proteins.” 2015. Web. 15 Feb 2019.

Vancouver:

Zeng M. Investigations into the roles and molecular mechanisms of LanC-like proteins. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/78713.

Council of Science Editors:

Zeng M. Investigations into the roles and molecular mechanisms of LanC-like proteins. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/78713


University of Illinois – Urbana-Champaign

6. Tang, Weixin. Mechanistic studies of lanthipeptide biosynthesis.

Degree: PhD, Chemistry, 2015, University of Illinois – Urbana-Champaign

 Natural products and natural product derivatives have been the leading source of pharmaceutical compounds since the initial application of modern medicine. To fight the increasing… (more)

Subjects/Keywords: Enzyme mechanism; Lanthipeptide

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APA (6th Edition):

Tang, W. (2015). Mechanistic studies of lanthipeptide biosynthesis. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/78752

Chicago Manual of Style (16th Edition):

Tang, Weixin. “Mechanistic studies of lanthipeptide biosynthesis.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/78752.

MLA Handbook (7th Edition):

Tang, Weixin. “Mechanistic studies of lanthipeptide biosynthesis.” 2015. Web. 15 Feb 2019.

Vancouver:

Tang W. Mechanistic studies of lanthipeptide biosynthesis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/78752.

Council of Science Editors:

Tang W. Mechanistic studies of lanthipeptide biosynthesis. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/78752


University of Illinois – Urbana-Champaign

7. Garcia De Gonzalo, Chantal V. Studies on the mechanism of action of the antimicrobial S-linked glycopeptide sublancin.

Degree: PhD, Chemistry, 2015, University of Illinois – Urbana-Champaign

 Infectious diseases are a continuing threat to human health. In particular, the rapid development of bacterial antibiotic resistance not only decreases the effectiveness of known… (more)

Subjects/Keywords: Glycocin; Ribosomally synthesized and post-translationally modified peptide (RiPP); Antimicrobial; S-Linked

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APA (6th Edition):

Garcia De Gonzalo, C. V. (2015). Studies on the mechanism of action of the antimicrobial S-linked glycopeptide sublancin. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89179

Chicago Manual of Style (16th Edition):

Garcia De Gonzalo, Chantal V. “Studies on the mechanism of action of the antimicrobial S-linked glycopeptide sublancin.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/89179.

MLA Handbook (7th Edition):

Garcia De Gonzalo, Chantal V. “Studies on the mechanism of action of the antimicrobial S-linked glycopeptide sublancin.” 2015. Web. 15 Feb 2019.

Vancouver:

Garcia De Gonzalo CV. Studies on the mechanism of action of the antimicrobial S-linked glycopeptide sublancin. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/89179.

Council of Science Editors:

Garcia De Gonzalo CV. Studies on the mechanism of action of the antimicrobial S-linked glycopeptide sublancin. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89179


University of Illinois – Urbana-Champaign

8. Yang, Xiao. Biosynthesis and engineering of lanthipeptide natural products for novel applications.

Degree: PhD, Chemistry, 2015, University of Illinois – Urbana-Champaign

 Natural products have played prominent roles in science and medicine due to their diverse chemical scaffolds and biological activities. Ribosomally synthesized and post-translationally modified peptides… (more)

Subjects/Keywords: Lanthipeptide; Lantibiotic; natural product; biosynthesis

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APA (6th Edition):

Yang, X. (2015). Biosynthesis and engineering of lanthipeptide natural products for novel applications. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89185

Chicago Manual of Style (16th Edition):

Yang, Xiao. “Biosynthesis and engineering of lanthipeptide natural products for novel applications.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/89185.

MLA Handbook (7th Edition):

Yang, Xiao. “Biosynthesis and engineering of lanthipeptide natural products for novel applications.” 2015. Web. 15 Feb 2019.

Vancouver:

Yang X. Biosynthesis and engineering of lanthipeptide natural products for novel applications. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/89185.

Council of Science Editors:

Yang X. Biosynthesis and engineering of lanthipeptide natural products for novel applications. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89185


University of Illinois – Urbana-Champaign

9. Ortega, Manuel A. Biochemical characterization of enzymes involved in the post-translational modification of lantibiotics.

Degree: PhD, Biochemistry, 2015, University of Illinois – Urbana-Champaign

 Lantibiotics are ribosomally-synthesized and post-translationally modified peptides (RiPPs) characterized for exerting antimicrobial activity against bacterial strains resistant to commonly used antibiotics. During lantibiotic biosynthesis different… (more)

Subjects/Keywords: antibiotics; biosynthesis; enzymology; X-ray crystallography; biochemistry; tRNA biology; natural products; ribosomal peptide natural products; Ribosomally synthesized and post-translationally modified peptides (RiPPs); Lantipeptides; Lanthipeptides; Lantibiotics; leader peptide; nisin; microbisporicin; NAI-107; dehydration; thioether; epilancin 15x; halogenation; decarboxylation; proteolysis; combinatorial biosynthesis; post-translational modifications; glutamylation

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APA (6th Edition):

Ortega, M. A. (2015). Biochemical characterization of enzymes involved in the post-translational modification of lantibiotics. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89190

Chicago Manual of Style (16th Edition):

Ortega, Manuel A. “Biochemical characterization of enzymes involved in the post-translational modification of lantibiotics.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/89190.

MLA Handbook (7th Edition):

Ortega, Manuel A. “Biochemical characterization of enzymes involved in the post-translational modification of lantibiotics.” 2015. Web. 15 Feb 2019.

Vancouver:

Ortega MA. Biochemical characterization of enzymes involved in the post-translational modification of lantibiotics. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/89190.

Council of Science Editors:

Ortega MA. Biochemical characterization of enzymes involved in the post-translational modification of lantibiotics. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89190


University of Illinois – Urbana-Champaign

10. Yu, Yi. Mechanistic studies of class II lanthipeptide synthetases and yeast surface display of lanthipeptide leader peptides.

Degree: PhD, Biochemistry, 2015, University of Illinois – Urbana-Champaign

 Lanthipeptides are natural products that belong to the family of ribosomally synthesized and posttranslationally modified peptides (RiPPs). They contain the characteristic lanthionine (Lan) or methyllanthionine… (more)

Subjects/Keywords: Lanthipeptide; Lanthionine synthetase; Yeast surface display

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APA (6th Edition):

Yu, Y. (2015). Mechanistic studies of class II lanthipeptide synthetases and yeast surface display of lanthipeptide leader peptides. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89191

Chicago Manual of Style (16th Edition):

Yu, Yi. “Mechanistic studies of class II lanthipeptide synthetases and yeast surface display of lanthipeptide leader peptides.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/89191.

MLA Handbook (7th Edition):

Yu, Yi. “Mechanistic studies of class II lanthipeptide synthetases and yeast surface display of lanthipeptide leader peptides.” 2015. Web. 15 Feb 2019.

Vancouver:

Yu Y. Mechanistic studies of class II lanthipeptide synthetases and yeast surface display of lanthipeptide leader peptides. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/89191.

Council of Science Editors:

Yu Y. Mechanistic studies of class II lanthipeptide synthetases and yeast surface display of lanthipeptide leader peptides. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89191


University of Illinois – Urbana-Champaign

11. Shi, Yanxiang. Exploration of the biosynthesis of lanthipeptides.

Degree: PhD, 0335, 2014, University of Illinois – Urbana-Champaign

 Natural products play important roles in the survival of organisms, and provide a large pool of candidates for drug discovery and pharmaceutical investigations. A major… (more)

Subjects/Keywords: Lanthipeptides; Biosynthesis; Co-expression

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APA (6th Edition):

Shi, Y. (2014). Exploration of the biosynthesis of lanthipeptides. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/46855

Chicago Manual of Style (16th Edition):

Shi, Yanxiang. “Exploration of the biosynthesis of lanthipeptides.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/46855.

MLA Handbook (7th Edition):

Shi, Yanxiang. “Exploration of the biosynthesis of lanthipeptides.” 2014. Web. 15 Feb 2019.

Vancouver:

Shi Y. Exploration of the biosynthesis of lanthipeptides. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/46855.

Council of Science Editors:

Shi Y. Exploration of the biosynthesis of lanthipeptides. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/46855


University of Illinois – Urbana-Champaign

12. Garg, Neha. Exploring and understanding lantibiotic biosynthesis.

Degree: PhD, 0318, 2014, University of Illinois – Urbana-Champaign

 The ribosome translates genomic information into structural and catalytic protein molecules. In addition to its role in protein synthesis, the ribosome also produces small non-catalytic… (more)

Subjects/Keywords: Antibiotic resistance; Lantibiotic; Biosynthesis; Stereochemistry

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APA (6th Edition):

Garg, N. (2014). Exploring and understanding lantibiotic biosynthesis. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/46883

Chicago Manual of Style (16th Edition):

Garg, Neha. “Exploring and understanding lantibiotic biosynthesis.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/46883.

MLA Handbook (7th Edition):

Garg, Neha. “Exploring and understanding lantibiotic biosynthesis.” 2014. Web. 15 Feb 2019.

Vancouver:

Garg N. Exploring and understanding lantibiotic biosynthesis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/46883.

Council of Science Editors:

Garg N. Exploring and understanding lantibiotic biosynthesis. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/46883


University of Illinois – Urbana-Champaign

13. Hung, John. Mechanistic studies to determine the catalytic roles of active site residues in phosphite dehydrogenase.

Degree: PhD, 0335, 2014, University of Illinois – Urbana-Champaign

 Phosphite dehydrogenase (PTDH) catalyzes the oxidation of phosphite to phosphate with the concurrent reduction of NAD+ to NADH. The mechanism of the reaction resembles a… (more)

Subjects/Keywords: Phosphite Dehydrogenase; enzymology; chemical biology; enzymes; enzyme kinetics; enzyme inhibition

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APA (6th Edition):

Hung, J. (2014). Mechanistic studies to determine the catalytic roles of active site residues in phosphite dehydrogenase. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/46929

Chicago Manual of Style (16th Edition):

Hung, John. “Mechanistic studies to determine the catalytic roles of active site residues in phosphite dehydrogenase.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/46929.

MLA Handbook (7th Edition):

Hung, John. “Mechanistic studies to determine the catalytic roles of active site residues in phosphite dehydrogenase.” 2014. Web. 15 Feb 2019.

Vancouver:

Hung J. Mechanistic studies to determine the catalytic roles of active site residues in phosphite dehydrogenase. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/46929.

Council of Science Editors:

Hung J. Mechanistic studies to determine the catalytic roles of active site residues in phosphite dehydrogenase. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/46929


University of Illinois – Urbana-Champaign

14. Clark, Kevin M. Probing the roles of metal binding ligands in cupredoxins: incorporating nonproteinogenic amino acids into azurin and CuA Azurin.

Degree: PhD, 0318, 2010, University of Illinois – Urbana-Champaign

 Metalloproteins play important roles in biological systems since metal-binding sites are found in ~ 1/3 of structurally characterized proteins and in ~ 1/2 of all… (more)

Subjects/Keywords: Azurin; CuA Azurin; Expressed Protein Ligation; homocysteine; backbone ester; peptide ligation

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APA (6th Edition):

Clark, K. M. (2010). Probing the roles of metal binding ligands in cupredoxins: incorporating nonproteinogenic amino acids into azurin and CuA Azurin. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/17059

Chicago Manual of Style (16th Edition):

Clark, Kevin M. “Probing the roles of metal binding ligands in cupredoxins: incorporating nonproteinogenic amino acids into azurin and CuA Azurin.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/17059.

MLA Handbook (7th Edition):

Clark, Kevin M. “Probing the roles of metal binding ligands in cupredoxins: incorporating nonproteinogenic amino acids into azurin and CuA Azurin.” 2010. Web. 15 Feb 2019.

Vancouver:

Clark KM. Probing the roles of metal binding ligands in cupredoxins: incorporating nonproteinogenic amino acids into azurin and CuA Azurin. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/17059.

Council of Science Editors:

Clark KM. Probing the roles of metal binding ligands in cupredoxins: incorporating nonproteinogenic amino acids into azurin and CuA Azurin. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/17059


University of Illinois – Urbana-Champaign

15. Bindman, Noah. New chemical and biosynthetic methodologies for the study of lanthipeptides.

Degree: PhD, 0335, 2014, University of Illinois – Urbana-Champaign

 Recent genome sequencing efforts have revealed that a common biosynthetic route to peptide natural products involves ribosomally synthesized and posttranslationally modified peptides (RiPPs). One of… (more)

Subjects/Keywords: peptide natural product; ribosomally synthesized and posttranslationally modified peptide; Lanthionine; Lanthipeptide; methyllanthionine; bioengineering; posttranslational modification; photochemical linker; lacticin 481; nukacin ISK-1; haloduracin; prochlorosin; nisin; hydroxy acid; pyrrolysyl tRNA; α-ketoamide; fluorescently modified lantibiotic

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APA (6th Edition):

Bindman, N. (2014). New chemical and biosynthetic methodologies for the study of lanthipeptides. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/49785

Chicago Manual of Style (16th Edition):

Bindman, Noah. “New chemical and biosynthetic methodologies for the study of lanthipeptides.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/49785.

MLA Handbook (7th Edition):

Bindman, Noah. “New chemical and biosynthetic methodologies for the study of lanthipeptides.” 2014. Web. 15 Feb 2019.

Vancouver:

Bindman N. New chemical and biosynthetic methodologies for the study of lanthipeptides. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/49785.

Council of Science Editors:

Bindman N. New chemical and biosynthetic methodologies for the study of lanthipeptides. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/49785


University of Illinois – Urbana-Champaign

16. Okesli, Ayse. Biosynthesis and engineering of lanthipeptides.

Degree: PhD, 0335, 2014, University of Illinois – Urbana-Champaign

 The emergence of antibiotic-resistant bacterial strains is a growing concern as antimicrobial drug discovery is not proceeding at the same pace as the growth of… (more)

Subjects/Keywords: Lanthipeptides; cinnamycin; nisin; Phage display; biosynthesis of natural products; Lantibiotics

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APA (6th Edition):

Okesli, A. (2014). Biosynthesis and engineering of lanthipeptides. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/50336

Chicago Manual of Style (16th Edition):

Okesli, Ayse. “Biosynthesis and engineering of lanthipeptides.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/50336.

MLA Handbook (7th Edition):

Okesli, Ayse. “Biosynthesis and engineering of lanthipeptides.” 2014. Web. 15 Feb 2019.

Vancouver:

Okesli A. Biosynthesis and engineering of lanthipeptides. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/50336.

Council of Science Editors:

Okesli A. Biosynthesis and engineering of lanthipeptides. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/50336


University of Illinois – Urbana-Champaign

17. Knerr, Patrick. Chemical and chemoenzymatic syntheses of lantibiotics and other bioactive cyclic peptides.

Degree: PhD, 0335, 2013, University of Illinois – Urbana-Champaign

 New antibiotics are desperately needed to combat the disturbing rise of pathogenic microorganisms resistant to traditional treatments. Throughout the history of modern medicine, natural products… (more)

Subjects/Keywords: Lantibiotics; Lanthipeptides; natural products; epilancin 15X; lacticin 481; LctM; compstatin; ribosomally synthesized and post-translationally modified peptides; RiPPs; post-translational modification; cyclic peptides; antibiotics; peptide synthesis; solid-phase peptide synthesis (SPPS); biosynthetic engineering; thioether; structure-activity relationship; disulfide engineering

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APA (6th Edition):

Knerr, P. (2013). Chemical and chemoenzymatic syntheses of lantibiotics and other bioactive cyclic peptides. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/44475

Chicago Manual of Style (16th Edition):

Knerr, Patrick. “Chemical and chemoenzymatic syntheses of lantibiotics and other bioactive cyclic peptides.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/44475.

MLA Handbook (7th Edition):

Knerr, Patrick. “Chemical and chemoenzymatic syntheses of lantibiotics and other bioactive cyclic peptides.” 2013. Web. 15 Feb 2019.

Vancouver:

Knerr P. Chemical and chemoenzymatic syntheses of lantibiotics and other bioactive cyclic peptides. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/44475.

Council of Science Editors:

Knerr P. Chemical and chemoenzymatic syntheses of lantibiotics and other bioactive cyclic peptides. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/44475


University of Illinois – Urbana-Champaign

18. Lee, Jin Hee. Investigation of the biosynthesis of the phosphonate antibiotics bialaphos and dehydrophos.

Degree: PhD, 0335, 2010, University of Illinois – Urbana-Champaign

 Phosphonate and phosphinate natural products possess a range of biological activities as a result of their ability to mimic phosphate esters or tetrahedral intermediates formed… (more)

Subjects/Keywords: phosphonate antibiotics; bialaphos; dehydrophos; nonribosomal peptide synthetase; phosphinothricin; methyltransferase; biosynthesis

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APA (6th Edition):

Lee, J. H. (2010). Investigation of the biosynthesis of the phosphonate antibiotics bialaphos and dehydrophos. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/17000

Chicago Manual of Style (16th Edition):

Lee, Jin Hee. “Investigation of the biosynthesis of the phosphonate antibiotics bialaphos and dehydrophos.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/17000.

MLA Handbook (7th Edition):

Lee, Jin Hee. “Investigation of the biosynthesis of the phosphonate antibiotics bialaphos and dehydrophos.” 2010. Web. 15 Feb 2019.

Vancouver:

Lee JH. Investigation of the biosynthesis of the phosphonate antibiotics bialaphos and dehydrophos. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/17000.

Council of Science Editors:

Lee JH. Investigation of the biosynthesis of the phosphonate antibiotics bialaphos and dehydrophos. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/17000


University of Illinois – Urbana-Champaign

19. Whitteck, John T. Investigation of phosphonate biosynthesis: I. Structure of dehydrophos II. Mechanism of hydroxyethylphosphonate dioxygenase.

Degree: PhD, 0335, 2010, University of Illinois – Urbana-Champaign

 Natural product phosphonates are used extensively in the clinic as antibacterials and in commercial agriculture as herbicides. In an effort to efficiently discover new natural… (more)

Subjects/Keywords: biosynthesis; phosphonate; dehydrophos; phosphinothricin; hydroxyethylphosphonate dioxygenase

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APA (6th Edition):

Whitteck, J. T. (2010). Investigation of phosphonate biosynthesis: I. Structure of dehydrophos II. Mechanism of hydroxyethylphosphonate dioxygenase. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/17023

Chicago Manual of Style (16th Edition):

Whitteck, John T. “Investigation of phosphonate biosynthesis: I. Structure of dehydrophos II. Mechanism of hydroxyethylphosphonate dioxygenase.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/17023.

MLA Handbook (7th Edition):

Whitteck, John T. “Investigation of phosphonate biosynthesis: I. Structure of dehydrophos II. Mechanism of hydroxyethylphosphonate dioxygenase.” 2010. Web. 15 Feb 2019.

Vancouver:

Whitteck JT. Investigation of phosphonate biosynthesis: I. Structure of dehydrophos II. Mechanism of hydroxyethylphosphonate dioxygenase. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/17023.

Council of Science Editors:

Whitteck JT. Investigation of phosphonate biosynthesis: I. Structure of dehydrophos II. Mechanism of hydroxyethylphosphonate dioxygenase. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/17023


University of Illinois – Urbana-Champaign

20. Velasquez, Juan. Biosynthesis of the antimicrobial peptide epilancin 15X.

Degree: PhD, 0335, 2012, University of Illinois – Urbana-Champaign

 Lantibiotics are polycyclic antimicrobial peptides that are ribosomally synthesized and posttranslationally modified to their biologically active forms. The recently discovered lantibiotic epilancin 15X produced by… (more)

Subjects/Keywords: Antibiotics; Lantibiotics; Epilancin 15X; Nisin; Antimicrobial peptides; Biosynthesis; Natural Products; Short-Chain Dehydrogenase/Reductase; Serine proteases; Phosphonates

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APA (6th Edition):

Velasquez, J. (2012). Biosynthesis of the antimicrobial peptide epilancin 15X. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/29545

Chicago Manual of Style (16th Edition):

Velasquez, Juan. “Biosynthesis of the antimicrobial peptide epilancin 15X.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/29545.

MLA Handbook (7th Edition):

Velasquez, Juan. “Biosynthesis of the antimicrobial peptide epilancin 15X.” 2012. Web. 15 Feb 2019.

Vancouver:

Velasquez J. Biosynthesis of the antimicrobial peptide epilancin 15X. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/29545.

Council of Science Editors:

Velasquez J. Biosynthesis of the antimicrobial peptide epilancin 15X. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/29545


University of Illinois – Urbana-Champaign

21. Frisz, Jessica. Using imaging secondary ion mass spectrometry to determine mammalian plasma membrane component distribution and cell differentiation state.

Degree: PhD, 0335, 2012, University of Illinois – Urbana-Champaign

 The organization of the plasma membranes of mammalian cells has been studied for over forty years, with our understanding evolving from the fluid mosaic model… (more)

Subjects/Keywords: Secondary ion mass spectrometry (SIMS); Plasma membrane; Sphingolipids; Cholesterol; Time-of-flight SIMS; Multivariate analysis; Differentiation

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APA (6th Edition):

Frisz, J. (2012). Using imaging secondary ion mass spectrometry to determine mammalian plasma membrane component distribution and cell differentiation state. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/32025

Chicago Manual of Style (16th Edition):

Frisz, Jessica. “Using imaging secondary ion mass spectrometry to determine mammalian plasma membrane component distribution and cell differentiation state.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/32025.

MLA Handbook (7th Edition):

Frisz, Jessica. “Using imaging secondary ion mass spectrometry to determine mammalian plasma membrane component distribution and cell differentiation state.” 2012. Web. 15 Feb 2019.

Vancouver:

Frisz J. Using imaging secondary ion mass spectrometry to determine mammalian plasma membrane component distribution and cell differentiation state. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/32025.

Council of Science Editors:

Frisz J. Using imaging secondary ion mass spectrometry to determine mammalian plasma membrane component distribution and cell differentiation state. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/32025


University of Illinois – Urbana-Champaign

22. Smith, Sheena. Engineering and characterization of human single-chain T cell receptors.

Degree: PhD, 0318, 2015, University of Illinois – Urbana-Champaign

 All nucleated cells display a sampling of their protein contents in the form of short 9-10 amino acid peptides bound to a product of the… (more)

Subjects/Keywords: T cell receptors; yeast display; protein engineering; directed evolution; peptide major histocompatibility complex (MHC) antigens

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APA (6th Edition):

Smith, S. (2015). Engineering and characterization of human single-chain T cell receptors. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/72953

Chicago Manual of Style (16th Edition):

Smith, Sheena. “Engineering and characterization of human single-chain T cell receptors.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/72953.

MLA Handbook (7th Edition):

Smith, Sheena. “Engineering and characterization of human single-chain T cell receptors.” 2015. Web. 15 Feb 2019.

Vancouver:

Smith S. Engineering and characterization of human single-chain T cell receptors. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/72953.

Council of Science Editors:

Smith S. Engineering and characterization of human single-chain T cell receptors. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/72953


University of Illinois – Urbana-Champaign

23. Ghasem pur, Salehe. Mining the enolase superfamily for new functions: investigations of D-glucarate dehydratase related proteins (GlucDRP) and L-lyxonate dehydratase proteins (LyxD).

Degree: PhD, 0318, 2015, University of Illinois – Urbana-Champaign

 Genomic era begins with development of sequencing methods. Genome sequencing is now cost-effective and fast, giving rise to increasing amounts of genomic data. However, the… (more)

Subjects/Keywords: Enolase; L-lyxonate; Heterodimer; Heterospecies; D-Glucarate

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APA (6th Edition):

Ghasem pur, S. (2015). Mining the enolase superfamily for new functions: investigations of D-glucarate dehydratase related proteins (GlucDRP) and L-lyxonate dehydratase proteins (LyxD). (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/73056

Chicago Manual of Style (16th Edition):

Ghasem pur, Salehe. “Mining the enolase superfamily for new functions: investigations of D-glucarate dehydratase related proteins (GlucDRP) and L-lyxonate dehydratase proteins (LyxD).” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/73056.

MLA Handbook (7th Edition):

Ghasem pur, Salehe. “Mining the enolase superfamily for new functions: investigations of D-glucarate dehydratase related proteins (GlucDRP) and L-lyxonate dehydratase proteins (LyxD).” 2015. Web. 15 Feb 2019.

Vancouver:

Ghasem pur S. Mining the enolase superfamily for new functions: investigations of D-glucarate dehydratase related proteins (GlucDRP) and L-lyxonate dehydratase proteins (LyxD). [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/73056.

Council of Science Editors:

Ghasem pur S. Mining the enolase superfamily for new functions: investigations of D-glucarate dehydratase related proteins (GlucDRP) and L-lyxonate dehydratase proteins (LyxD). [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/73056


University of Illinois – Urbana-Champaign

24. Dunbar, Kyle. Revealing the molecular details of azoline formation in ribosomal natural product biosynthesis.

Degree: PhD, 0335, 2015, University of Illinois – Urbana-Champaign

 The thiazole/oxazole-modified microcins (TOMMs) are a recently grouped class of ribosomally synthesized and posttranslationally modified peptides. Encoded by many bacteria and archaea, these natural products… (more)

Subjects/Keywords: Azoline Biosynthesis; ribosomally synthesized and post-translationally modified peptide (RiPP) Biosynthesis; thiazole/oxazole-modified microcin (TOMM) Biosynthesis; Cyclodehydratase; YcaO

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APA (6th Edition):

Dunbar, K. (2015). Revealing the molecular details of azoline formation in ribosomal natural product biosynthesis. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/73109

Chicago Manual of Style (16th Edition):

Dunbar, Kyle. “Revealing the molecular details of azoline formation in ribosomal natural product biosynthesis.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/73109.

MLA Handbook (7th Edition):

Dunbar, Kyle. “Revealing the molecular details of azoline formation in ribosomal natural product biosynthesis.” 2015. Web. 15 Feb 2019.

Vancouver:

Dunbar K. Revealing the molecular details of azoline formation in ribosomal natural product biosynthesis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/73109.

Council of Science Editors:

Dunbar K. Revealing the molecular details of azoline formation in ribosomal natural product biosynthesis. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/73109


University of Illinois – Urbana-Champaign

25. Sharma, Preeti. Engineering soluble, high affinity T cell receptor domains for detection of staphylococcal and streptococcal exotoxins.

Degree: PhD, Biochemistry, 2015, University of Illinois – Urbana-Champaign

 Staphylococcus aureus and group A Streptococcus express a family of exotoxins including staphylococcal enterotoxins A, B, C (SEA, SEB, SEC), toxic shock syndrome toxin-1 (TSST-1)… (more)

Subjects/Keywords: Staphylococcus aureus; Streptococcus pyogenes; superantigens; yeast display; directed evolution; affinity maturation, T cell receptors; staphylococcal enterotoxin A (SEA); food poisoning; multiplex assay

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APA (6th Edition):

Sharma, P. (2015). Engineering soluble, high affinity T cell receptor domains for detection of staphylococcal and streptococcal exotoxins. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/78741

Chicago Manual of Style (16th Edition):

Sharma, Preeti. “Engineering soluble, high affinity T cell receptor domains for detection of staphylococcal and streptococcal exotoxins.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/78741.

MLA Handbook (7th Edition):

Sharma, Preeti. “Engineering soluble, high affinity T cell receptor domains for detection of staphylococcal and streptococcal exotoxins.” 2015. Web. 15 Feb 2019.

Vancouver:

Sharma P. Engineering soluble, high affinity T cell receptor domains for detection of staphylococcal and streptococcal exotoxins. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/78741.

Council of Science Editors:

Sharma P. Engineering soluble, high affinity T cell receptor domains for detection of staphylococcal and streptococcal exotoxins. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/78741


University of Illinois – Urbana-Champaign

26. Yasui, Norio. I. Facile preparation of ortho-fluorophenols from non-aromatic precursors and investigation of applications to fluorine-18 labeling II. Resin-supported silyl ester precursors for kit-like radiolabeling with fluorine-18.

Degree: PhD, Chemistry, 2015, University of Illinois – Urbana-Champaign

 Molecular imaging is a technique that can be used to visualize complex biochemical processes without perturbing living organisms, and it has been playing increasingly important… (more)

Subjects/Keywords: fluorine-18; radiochemistry; fluorination; diazoketone; silyl ester; resin-supported

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APA (6th Edition):

Yasui, N. (2015). I. Facile preparation of ortho-fluorophenols from non-aromatic precursors and investigation of applications to fluorine-18 labeling II. Resin-supported silyl ester precursors for kit-like radiolabeling with fluorine-18. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/88254

Chicago Manual of Style (16th Edition):

Yasui, Norio. “I. Facile preparation of ortho-fluorophenols from non-aromatic precursors and investigation of applications to fluorine-18 labeling II. Resin-supported silyl ester precursors for kit-like radiolabeling with fluorine-18.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/88254.

MLA Handbook (7th Edition):

Yasui, Norio. “I. Facile preparation of ortho-fluorophenols from non-aromatic precursors and investigation of applications to fluorine-18 labeling II. Resin-supported silyl ester precursors for kit-like radiolabeling with fluorine-18.” 2015. Web. 15 Feb 2019.

Vancouver:

Yasui N. I. Facile preparation of ortho-fluorophenols from non-aromatic precursors and investigation of applications to fluorine-18 labeling II. Resin-supported silyl ester precursors for kit-like radiolabeling with fluorine-18. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/88254.

Council of Science Editors:

Yasui N. I. Facile preparation of ortho-fluorophenols from non-aromatic precursors and investigation of applications to fluorine-18 labeling II. Resin-supported silyl ester precursors for kit-like radiolabeling with fluorine-18. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/88254


University of Illinois – Urbana-Champaign

27. Cox, Courtney Lynne. Strategies for thiazole/oxazole-modified microcin discovery.

Degree: PhD, Microbiology, 2015, University of Illinois – Urbana-Champaign

 Natural products continue to be an important source of therapeutically-relevant compounds. With the advent of inexpensive genome sequencing it has become apparent that bacteria produce… (more)

Subjects/Keywords: antibiotic discovery

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APA (6th Edition):

Cox, C. L. (2015). Strategies for thiazole/oxazole-modified microcin discovery. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/88284

Chicago Manual of Style (16th Edition):

Cox, Courtney Lynne. “Strategies for thiazole/oxazole-modified microcin discovery.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/88284.

MLA Handbook (7th Edition):

Cox, Courtney Lynne. “Strategies for thiazole/oxazole-modified microcin discovery.” 2015. Web. 15 Feb 2019.

Vancouver:

Cox CL. Strategies for thiazole/oxazole-modified microcin discovery. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/88284.

Council of Science Editors:

Cox CL. Strategies for thiazole/oxazole-modified microcin discovery. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/88284


University of Illinois – Urbana-Champaign

28. Parkinson, Elizabeth Ivy. Deoxynyboquinones as NQO1-targeted anticancer compounds and deoxynybomycins as potent and selective antibiotics.

Degree: PhD, Chemistry, 2015, University of Illinois – Urbana-Champaign

 Cancer and antibiotic-resistant bacterial infections are currently two of the major health concerns facing the United States. Novel therapeutics capable of specifically targeting either cancer… (more)

Subjects/Keywords: NAD(P)H:quinone oxidoreductase-1 (NQO1); reduction-oxidation cycling; deoxynyboquinone; anticancer; fluoroquinolones; antibiotic resistance; deoxynybomycin; DNA gyrase

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APA (6th Edition):

Parkinson, E. I. (2015). Deoxynyboquinones as NQO1-targeted anticancer compounds and deoxynybomycins as potent and selective antibiotics. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89176

Chicago Manual of Style (16th Edition):

Parkinson, Elizabeth Ivy. “Deoxynyboquinones as NQO1-targeted anticancer compounds and deoxynybomycins as potent and selective antibiotics.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/89176.

MLA Handbook (7th Edition):

Parkinson, Elizabeth Ivy. “Deoxynyboquinones as NQO1-targeted anticancer compounds and deoxynybomycins as potent and selective antibiotics.” 2015. Web. 15 Feb 2019.

Vancouver:

Parkinson EI. Deoxynyboquinones as NQO1-targeted anticancer compounds and deoxynybomycins as potent and selective antibiotics. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/89176.

Council of Science Editors:

Parkinson EI. Deoxynyboquinones as NQO1-targeted anticancer compounds and deoxynybomycins as potent and selective antibiotics. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89176


University of Illinois – Urbana-Champaign

29. Li, Ying. Responsive molecules: 1. Redox-responsive quadruple hydrogen bonding unit 2. Crosslinked dendronized polyols for brighter and more stable dyes 3. Photoresponsive proton gate for cross-membrane transfer.

Degree: PhD, Chemistry, 2016, University of Illinois – Urbana-Champaign

 This thesis reports studies in three separate contexts that show how responsiveness can be introduced or tuned in different molecular systems thus providing desirable control… (more)

Subjects/Keywords: stimuli-responsive

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APA (6th Edition):

Li, Y. (2016). Responsive molecules: 1. Redox-responsive quadruple hydrogen bonding unit 2. Crosslinked dendronized polyols for brighter and more stable dyes 3. Photoresponsive proton gate for cross-membrane transfer. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/90531

Chicago Manual of Style (16th Edition):

Li, Ying. “Responsive molecules: 1. Redox-responsive quadruple hydrogen bonding unit 2. Crosslinked dendronized polyols for brighter and more stable dyes 3. Photoresponsive proton gate for cross-membrane transfer.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/90531.

MLA Handbook (7th Edition):

Li, Ying. “Responsive molecules: 1. Redox-responsive quadruple hydrogen bonding unit 2. Crosslinked dendronized polyols for brighter and more stable dyes 3. Photoresponsive proton gate for cross-membrane transfer.” 2016. Web. 15 Feb 2019.

Vancouver:

Li Y. Responsive molecules: 1. Redox-responsive quadruple hydrogen bonding unit 2. Crosslinked dendronized polyols for brighter and more stable dyes 3. Photoresponsive proton gate for cross-membrane transfer. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/90531.

Council of Science Editors:

Li Y. Responsive molecules: 1. Redox-responsive quadruple hydrogen bonding unit 2. Crosslinked dendronized polyols for brighter and more stable dyes 3. Photoresponsive proton gate for cross-membrane transfer. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/90531

30. Chandrasekar, Jagadeeswaran. DNA catalysts as phosphatases and as phosphoserine lyases.

Degree: PhD, Chemistry, 2016, University of Illinois – Urbana-Champaign

 Proteins and RNA are the only known biopolymers that have catalytic roles in nature, whereas DNA is primarily considered to store and transfer genetic information.… (more)

Subjects/Keywords: DNA Catalysts; Phosphatase; Phosphoserine Lyase; In vitro selection

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

APA (6th Edition):

Chandrasekar, J. (2016). DNA catalysts as phosphatases and as phosphoserine lyases. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/90607

Chicago Manual of Style (16th Edition):

Chandrasekar, Jagadeeswaran. “DNA catalysts as phosphatases and as phosphoserine lyases.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 15, 2019. http://hdl.handle.net/2142/90607.

MLA Handbook (7th Edition):

Chandrasekar, Jagadeeswaran. “DNA catalysts as phosphatases and as phosphoserine lyases.” 2016. Web. 15 Feb 2019.

Vancouver:

Chandrasekar J. DNA catalysts as phosphatases and as phosphoserine lyases. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Feb 15]. Available from: http://hdl.handle.net/2142/90607.

Council of Science Editors:

Chandrasekar J. DNA catalysts as phosphatases and as phosphoserine lyases. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/90607

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