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You searched for +publisher:"University of Illinois – Urbana-Champaign" +contributor:("Mitchell, Douglas A."). Showing records 1 – 30 of 38 total matches.

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University of Illinois – Urbana-Champaign

1. Molohon Hess, Katie Jo. Structure and function analysis of the natural product plantazolicin, a bacillus anthracis-specific antibiotic.

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

 Bacteria are a fruitful source of metabolites, many of which have been the scaffolds for the majority of approved antibiotic compounds. In this dissertation, I… (more)

Subjects/Keywords: Plantazolicin; Natural product; Bacillus anthracis; Mode of action

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APA (6th Edition):

Molohon Hess, K. J. (2015). Structure and function analysis of the natural product plantazolicin, a bacillus anthracis-specific antibiotic. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89125

Chicago Manual of Style (16th Edition):

Molohon Hess, Katie Jo. “Structure and function analysis of the natural product plantazolicin, a bacillus anthracis-specific antibiotic.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/89125.

MLA Handbook (7th Edition):

Molohon Hess, Katie Jo. “Structure and function analysis of the natural product plantazolicin, a bacillus anthracis-specific antibiotic.” 2015. Web. 26 Aug 2019.

Vancouver:

Molohon Hess KJ. Structure and function analysis of the natural product plantazolicin, a bacillus anthracis-specific antibiotic. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/89125.

Council of Science Editors:

Molohon Hess KJ. Structure and function analysis of the natural product plantazolicin, a bacillus anthracis-specific antibiotic. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89125


University of Illinois – Urbana-Champaign

2. Blair, Patricia M. Discovery and characterization of ribosomally synthesized and post-translationally modified peptide natural products.

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

 Bacterial secondary metabolites have historically been a rich source of antibiotic compounds. The genomic era has shown that bacteria harbor the potential to produce even… (more)

Subjects/Keywords: Ribosomally synthesized and post-translationally modified peptide; Natural products; Chemical probes; Mode of action

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APA (6th Edition):

Blair, P. M. (2016). Discovery and characterization of ribosomally synthesized and post-translationally modified peptide natural products. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95476

Chicago Manual of Style (16th Edition):

Blair, Patricia M. “Discovery and characterization of ribosomally synthesized and post-translationally modified peptide natural products.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/95476.

MLA Handbook (7th Edition):

Blair, Patricia M. “Discovery and characterization of ribosomally synthesized and post-translationally modified peptide natural products.” 2016. Web. 26 Aug 2019.

Vancouver:

Blair PM. Discovery and characterization of ribosomally synthesized and post-translationally modified peptide natural products. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/95476.

Council of Science Editors:

Blair PM. Discovery and characterization of ribosomally synthesized and post-translationally modified peptide natural products. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95476


University of Illinois – Urbana-Champaign

3. Tietz, Jonathan I. Genomics as a tool for natural product structure elucidation.

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

 Natural product discovery is in the midst of a transition from a largely serendipity-based effort to an informatics-driven one. For most of the 20th century,… (more)

Subjects/Keywords: natural products; antibiotics; bioinformatics; lasso peptides; structure elucidation; JBIR-100; streptomonomicin; biosynthesis

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APA (6th Edition):

Tietz, J. I. (2016). Genomics as a tool for natural product structure elucidation. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95593

Chicago Manual of Style (16th Edition):

Tietz, Jonathan I. “Genomics as a tool for natural product structure elucidation.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/95593.

MLA Handbook (7th Edition):

Tietz, Jonathan I. “Genomics as a tool for natural product structure elucidation.” 2016. Web. 26 Aug 2019.

Vancouver:

Tietz JI. Genomics as a tool for natural product structure elucidation. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/95593.

Council of Science Editors:

Tietz JI. Genomics as a tool for natural product structure elucidation. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95593


University of Illinois – Urbana-Champaign

4. 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 August 26, 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. 26 Aug 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 Aug 26]. 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

5. 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 August 26, 2019. http://hdl.handle.net/2142/88284.

MLA Handbook (7th Edition):

Cox, Courtney Lynne. “Strategies for thiazole/oxazole-modified microcin discovery.” 2015. Web. 26 Aug 2019.

Vancouver:

Cox CL. Strategies for thiazole/oxazole-modified microcin discovery. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Aug 26]. 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

6. Maxson, Tucker. Stimulating antibiotic development by targeting virulence and facilitating natural product discovery.

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

 Antibiotics are a cornerstone of modern medicine and have drastically reduced the burden of infectious diseases. Unfortunately, resistance to all clinically used antibiotics has become… (more)

Subjects/Keywords: virulence; nelfinavir; CaaX protease; natural products; reactivity based screening

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APA (6th Edition):

Maxson, T. (2016). Stimulating antibiotic development by targeting virulence and facilitating natural product discovery. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/90486

Chicago Manual of Style (16th Edition):

Maxson, Tucker. “Stimulating antibiotic development by targeting virulence and facilitating natural product discovery.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/90486.

MLA Handbook (7th Edition):

Maxson, Tucker. “Stimulating antibiotic development by targeting virulence and facilitating natural product discovery.” 2016. Web. 26 Aug 2019.

Vancouver:

Maxson T. Stimulating antibiotic development by targeting virulence and facilitating natural product discovery. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/90486.

Council of Science Editors:

Maxson T. Stimulating antibiotic development by targeting virulence and facilitating natural product discovery. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/90486


University of Illinois – Urbana-Champaign

7. Si, Tong. Genome engineering in saccharomyces cerevisiae.

Degree: PhD, 0300, 2015, University of Illinois – Urbana-Champaign

 Microbial cell factory, which converts biomass feedstock to value-added compounds such as fuels, chemicals, materials and pharmaceuticals, has been proposed as a sustainable and renewable… (more)

Subjects/Keywords: Genome Engineering; metabolic engineering; RNA interference; high-throughput screen; clustered regularly interspaced short palindromic repeats (CRISPR); synthetic biology; microbial cell factory

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APA (6th Edition):

Si, T. (2015). Genome engineering in saccharomyces cerevisiae. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/73088

Chicago Manual of Style (16th Edition):

Si, Tong. “Genome engineering in saccharomyces cerevisiae.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/73088.

MLA Handbook (7th Edition):

Si, Tong. “Genome engineering in saccharomyces cerevisiae.” 2015. Web. 26 Aug 2019.

Vancouver:

Si T. Genome engineering in saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/73088.

Council of Science Editors:

Si T. Genome engineering in saccharomyces cerevisiae. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/73088


University of Illinois – Urbana-Champaign

8. Zhu, Wei. Targeting isoprenoid biosynthesis for drug discovery.

Degree: PhD, 0319, 2013, University of Illinois – Urbana-Champaign

 Cancer and infectious diseases are huge threats to human beings. With the rapid rise in drug resistance, there is a need for new drugs, and… (more)

Subjects/Keywords: drug discovery; in silico high-throughput screening; peptidoglycan; protein structure; undecaprenyl diphosphate synthase (UPPS); farnesyl diphosphate synthase (FPPS); Deoxyribonucleic acid (DNA)

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APA (6th Edition):

Zhu, W. (2013). Targeting isoprenoid biosynthesis for drug discovery. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/45658

Chicago Manual of Style (16th Edition):

Zhu, Wei. “Targeting isoprenoid biosynthesis for drug discovery.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/45658.

MLA Handbook (7th Edition):

Zhu, Wei. “Targeting isoprenoid biosynthesis for drug discovery.” 2013. Web. 26 Aug 2019.

Vancouver:

Zhu W. Targeting isoprenoid biosynthesis for drug discovery. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/45658.

Council of Science Editors:

Zhu W. Targeting isoprenoid biosynthesis for drug discovery. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/45658


University of Illinois – Urbana-Champaign

9. Lambrecht, Michael. The chemical and enzymatic synthesis of poly(ADP-ribose).

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

 Poly(ADP-ribose) synthesis and degradation are important cellular processes associated with the DNA damage response and many other pathways. Traditionally, these processes have been challenging to… (more)

Subjects/Keywords: Poly(ADP-ribose); Total Synthesis; Enzymatic Synthesis; Poly(ADP-ribose) Polymerase; Poly ADP ribose polymerase (PARP); Poly(ADP-ribose) Glycohydrolase (PARG); Raptinal

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APA (6th Edition):

Lambrecht, M. (2016). The chemical and enzymatic synthesis of poly(ADP-ribose). (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/92923

Chicago Manual of Style (16th Edition):

Lambrecht, Michael. “The chemical and enzymatic synthesis of poly(ADP-ribose).” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/92923.

MLA Handbook (7th Edition):

Lambrecht, Michael. “The chemical and enzymatic synthesis of poly(ADP-ribose).” 2016. Web. 26 Aug 2019.

Vancouver:

Lambrecht M. The chemical and enzymatic synthesis of poly(ADP-ribose). [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/92923.

Council of Science Editors:

Lambrecht M. The chemical and enzymatic synthesis of poly(ADP-ribose). [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/92923


University of Illinois – Urbana-Champaign

10. Liu, Yi-Liang. Structure, function and inhibition of GcpE, FPPS and GGPPS: targeting isoprenoid biosynthesis for drug discovery.

Degree: PhD, 0319, 2013, University of Illinois – Urbana-Champaign

 IspG, farnesyl diphosphate synthase (FPPS) and geranylgeranyl diphosphate synthase (GGPPS) are enzymes involved in isoprenoid biosynthesis. Most bacterial IspGs contain two domains: a TIM barrel… (more)

Subjects/Keywords: X-ray Crystallography; Iron-sulfur protein; Catalysis; Drug Discovery; IspG; GcpE; geranylgeranyl diphosphate synthase (GGPPS); farnesyl diphosphate synthase (FPPS)

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APA (6th Edition):

Liu, Y. (2013). Structure, function and inhibition of GcpE, FPPS and GGPPS: targeting isoprenoid biosynthesis for drug discovery. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/42471

Chicago Manual of Style (16th Edition):

Liu, Yi-Liang. “Structure, function and inhibition of GcpE, FPPS and GGPPS: targeting isoprenoid biosynthesis for drug discovery.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/42471.

MLA Handbook (7th Edition):

Liu, Yi-Liang. “Structure, function and inhibition of GcpE, FPPS and GGPPS: targeting isoprenoid biosynthesis for drug discovery.” 2013. Web. 26 Aug 2019.

Vancouver:

Liu Y. Structure, function and inhibition of GcpE, FPPS and GGPPS: targeting isoprenoid biosynthesis for drug discovery. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/42471.

Council of Science Editors:

Liu Y. Structure, function and inhibition of GcpE, FPPS and GGPPS: targeting isoprenoid biosynthesis for drug discovery. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/42471


University of Illinois – Urbana-Champaign

11. No, Joo Hwan. Drug discovery against malaria parasite: drug repositioning strategy.

Degree: PhD, 0319, 2011, University of Illinois – Urbana-Champaign

 Malaria, caused by Plasmodium spp., causes ~1 million deaths each year and there are ever present problems due to drug resistance. In this work, I… (more)

Subjects/Keywords: Drug discovery; Malaria

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APA (6th Edition):

No, J. H. (2011). Drug discovery against malaria parasite: drug repositioning strategy. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/26307

Chicago Manual of Style (16th Edition):

No, Joo Hwan. “Drug discovery against malaria parasite: drug repositioning strategy.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/26307.

MLA Handbook (7th Edition):

No, Joo Hwan. “Drug discovery against malaria parasite: drug repositioning strategy.” 2011. Web. 26 Aug 2019.

Vancouver:

No JH. Drug discovery against malaria parasite: drug repositioning strategy. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/26307.

Council of Science Editors:

No JH. Drug discovery against malaria parasite: drug repositioning strategy. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/26307


University of Illinois – Urbana-Champaign

12. Yang, Ning. Mass spectrometry-based characterization of cell-to-cell signaling molecules in the nervous system.

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

 Cell-to-cell signaling molecules are an important class of endogenous molecules which are responsible for cell-to-cell communication within organisms. Small molecules and peptides work as neurotransmitters… (more)

Subjects/Keywords: mass spectrometry; neuropeptide; signaling molecules; peptidomics; structure elucidation

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APA (6th Edition):

Yang, N. (2016). Mass spectrometry-based characterization of cell-to-cell signaling molecules in the nervous system. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95541

Chicago Manual of Style (16th Edition):

Yang, Ning. “Mass spectrometry-based characterization of cell-to-cell signaling molecules in the nervous system.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/95541.

MLA Handbook (7th Edition):

Yang, Ning. “Mass spectrometry-based characterization of cell-to-cell signaling molecules in the nervous system.” 2016. Web. 26 Aug 2019.

Vancouver:

Yang N. Mass spectrometry-based characterization of cell-to-cell signaling molecules in the nervous system. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/95541.

Council of Science Editors:

Yang N. Mass spectrometry-based characterization of cell-to-cell signaling molecules in the nervous system. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95541


University of Illinois – Urbana-Champaign

13. 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 August 26, 2019. http://hdl.handle.net/2142/73062.

MLA Handbook (7th Edition):

Peck, Spencer. “Mechanistic investigations of enzymes in phosphonate metabolism.” 2015. Web. 26 Aug 2019.

Vancouver:

Peck S. Mechanistic investigations of enzymes in phosphonate metabolism. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Aug 26]. 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

14. Banks, Jessica M. Biomolecularly and mechanically instructive materials for guiding cell-substrate interactions.

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

 Techniques that enable the creation of instructive biomaterials have the potential to advance our understanding and ability to guide cell fate and function. Benzophenone (BP)… (more)

Subjects/Keywords: Stem cell differentiation; Biomaterials; Hydrogels; Collagen scaffolds; Leukocyte rolling; Photolithography; Benzophenone

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APA (6th Edition):

Banks, J. M. (2015). Biomolecularly and mechanically instructive materials for guiding cell-substrate interactions. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/87987

Chicago Manual of Style (16th Edition):

Banks, Jessica M. “Biomolecularly and mechanically instructive materials for guiding cell-substrate interactions.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/87987.

MLA Handbook (7th Edition):

Banks, Jessica M. “Biomolecularly and mechanically instructive materials for guiding cell-substrate interactions.” 2015. Web. 26 Aug 2019.

Vancouver:

Banks JM. Biomolecularly and mechanically instructive materials for guiding cell-substrate interactions. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/87987.

Council of Science Editors:

Banks JM. Biomolecularly and mechanically instructive materials for guiding cell-substrate interactions. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/87987


University of Illinois – Urbana-Champaign

15. Roth, Howard Steven. Improving the process synthesis, potency, and pharmacokinetics of the anticancer compound PAC-1.

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

 PAC-1 is an ortho-hydroxy-N-acylhydrazone that induces apoptosis by chelation of antiapoptotic labile zinc, relieving zinc-mediated inhibition of procaspase-3. Favorable results from cell culture and in… (more)

Subjects/Keywords: first procaspase activating compound (PAC-1); procaspase-3; zinc

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APA (6th Edition):

Roth, H. S. (2015). Improving the process synthesis, potency, and pharmacokinetics of the anticancer compound PAC-1. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/88246

Chicago Manual of Style (16th Edition):

Roth, Howard Steven. “Improving the process synthesis, potency, and pharmacokinetics of the anticancer compound PAC-1.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/88246.

MLA Handbook (7th Edition):

Roth, Howard Steven. “Improving the process synthesis, potency, and pharmacokinetics of the anticancer compound PAC-1.” 2015. Web. 26 Aug 2019.

Vancouver:

Roth HS. Improving the process synthesis, potency, and pharmacokinetics of the anticancer compound PAC-1. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/88246.

Council of Science Editors:

Roth HS. Improving the process synthesis, potency, and pharmacokinetics of the anticancer compound PAC-1. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/88246


University of Illinois – Urbana-Champaign

16. 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 August 26, 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. 26 Aug 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 Aug 26]. 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

17. 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 August 26, 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. 26 Aug 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 Aug 26]. 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

18. Sekerak, Nina M. Touch-and-go chemistry: development of materials for and demonstration of a contact-initiated polymerization.

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

 My graduate research has focused on demonstrating the concept of a contact-initiated, or touch-and-go, reaction. One of the foundational concepts of organic chemistry is that… (more)

Subjects/Keywords: Touch-and-go chemistry; emulsion polymerization; dispersion polymerization; suspension polymerization; carboxypolystyrene; unsymmetrical peroxide; benzoyl peroxide; dimethylaniline

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APA (6th Edition):

Sekerak, N. M. (2015). Touch-and-go chemistry: development of materials for and demonstration of a contact-initiated polymerization. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89272

Chicago Manual of Style (16th Edition):

Sekerak, Nina M. “Touch-and-go chemistry: development of materials for and demonstration of a contact-initiated polymerization.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/89272.

MLA Handbook (7th Edition):

Sekerak, Nina M. “Touch-and-go chemistry: development of materials for and demonstration of a contact-initiated polymerization.” 2015. Web. 26 Aug 2019.

Vancouver:

Sekerak NM. Touch-and-go chemistry: development of materials for and demonstration of a contact-initiated polymerization. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/89272.

Council of Science Editors:

Sekerak NM. Touch-and-go chemistry: development of materials for and demonstration of a contact-initiated polymerization. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89272


University of Illinois – Urbana-Champaign

19. Brandsen, Benjamin M. DNA catalysts for amide bond cleavage and for lysine side chain modification.

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

 Nature is known to exploit both proteins and RNA as enzymes. No natural enzymes, however, have been discovered that are made of DNA. One can… (more)

Subjects/Keywords: Deoxyribozyme; Ribozyme; DNA enzyme; DNA catalyst; Protease

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APA (6th Edition):

Brandsen, B. M. (2016). DNA catalysts for amide bond cleavage and for lysine side chain modification. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/90458

Chicago Manual of Style (16th Edition):

Brandsen, Benjamin M. “DNA catalysts for amide bond cleavage and for lysine side chain modification.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/90458.

MLA Handbook (7th Edition):

Brandsen, Benjamin M. “DNA catalysts for amide bond cleavage and for lysine side chain modification.” 2016. Web. 26 Aug 2019.

Vancouver:

Brandsen BM. DNA catalysts for amide bond cleavage and for lysine side chain modification. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/90458.

Council of Science Editors:

Brandsen BM. DNA catalysts for amide bond cleavage and for lysine side chain modification. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/90458


University of Illinois – Urbana-Champaign

20. 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 August 26, 2019. http://hdl.handle.net/2142/46855.

MLA Handbook (7th Edition):

Shi, Yanxiang. “Exploration of the biosynthesis of lanthipeptides.” 2014. Web. 26 Aug 2019.

Vancouver:

Shi Y. Exploration of the biosynthesis of lanthipeptides. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Aug 26]. 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

21. Morrison, Karen. Chemical diversification and anticancer activity of natural products.

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

 Natural products have historically formed the backbone of modern drug discovery efforts, particularly for cancer and bacterial infections. Despite this privileged status, difficulties associated with… (more)

Subjects/Keywords: Organic Synthesis; Complexity to Diversity; Natural Products; Anticancer

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APA (6th Edition):

Morrison, K. (2014). Chemical diversification and anticancer activity of natural products. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/46894

Chicago Manual of Style (16th Edition):

Morrison, Karen. “Chemical diversification and anticancer activity of natural products.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/46894.

MLA Handbook (7th Edition):

Morrison, Karen. “Chemical diversification and anticancer activity of natural products.” 2014. Web. 26 Aug 2019.

Vancouver:

Morrison K. Chemical diversification and anticancer activity of natural products. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/46894.

Council of Science Editors:

Morrison K. Chemical diversification and anticancer activity of natural products. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/46894


University of Illinois – Urbana-Champaign

22. Brothers, Michael. Toxin-membrane interactions of Pasteurella multocida toxin and homologous domains.

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

 Toxin-membrane interactions are poorly understood on the molecular level due to the inherent difficulty of crystallizing membrane protein complexes and the large size (>50 kDa)… (more)

Subjects/Keywords: Nuclear magnetic resonance (NMR) spectroscopy; Pasteurella multocida toxin; Membrane Localization Domain; Four Helix Bundle

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APA (6th Edition):

Brothers, M. (2014). Toxin-membrane interactions of Pasteurella multocida toxin and homologous domains. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/49777

Chicago Manual of Style (16th Edition):

Brothers, Michael. “Toxin-membrane interactions of Pasteurella multocida toxin and homologous domains.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/49777.

MLA Handbook (7th Edition):

Brothers, Michael. “Toxin-membrane interactions of Pasteurella multocida toxin and homologous domains.” 2014. Web. 26 Aug 2019.

Vancouver:

Brothers M. Toxin-membrane interactions of Pasteurella multocida toxin and homologous domains. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/49777.

Council of Science Editors:

Brothers M. Toxin-membrane interactions of Pasteurella multocida toxin and homologous domains. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/49777


University of Illinois – Urbana-Champaign

23. 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 August 26, 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. 26 Aug 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 Aug 26]. 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

24. 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 August 26, 2019. http://hdl.handle.net/2142/50336.

MLA Handbook (7th Edition):

Okesli, Ayse. “Biosynthesis and engineering of lanthipeptides.” 2014. Web. 26 Aug 2019.

Vancouver:

Okesli A. Biosynthesis and engineering of lanthipeptides. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Aug 26]. 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

25. Dokukin, Victor. Catalysis by DNA enzymes: roles of lanthanide(III) ions and DNA aptamer modules.

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

 For many years scientists considered DNA and RNA to be merely the means for the storage and transmission of genetic information. Catalytic roles of some… (more)

Subjects/Keywords: DNA catalysis; DNA catalysts; DNA enzyme; Deoxyribozyme; DNAzyme; Lanthanide ions; DNA aptamers; Modular catalysts; modular DNA catalysts

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APA (6th Edition):

Dokukin, V. (2014). Catalysis by DNA enzymes: roles of lanthanide(III) ions and DNA aptamer modules. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/50587

Chicago Manual of Style (16th Edition):

Dokukin, Victor. “Catalysis by DNA enzymes: roles of lanthanide(III) ions and DNA aptamer modules.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/50587.

MLA Handbook (7th Edition):

Dokukin, Victor. “Catalysis by DNA enzymes: roles of lanthanide(III) ions and DNA aptamer modules.” 2014. Web. 26 Aug 2019.

Vancouver:

Dokukin V. Catalysis by DNA enzymes: roles of lanthanide(III) ions and DNA aptamer modules. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/50587.

Council of Science Editors:

Dokukin V. Catalysis by DNA enzymes: roles of lanthanide(III) ions and DNA aptamer modules. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/50587


University of Illinois – Urbana-Champaign

26. Botham, Rachel C. Development of PAC-1 as a privileged agent for combination chemotherapy.

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

 Elucidation of the molecular mechanisms of cancers has enabled the development of molecularly targeted chemotherapeutics capable of exploiting cancer-specific cellular alterations. Small-molecule activation of procaspase-3… (more)

Subjects/Keywords: caspase; cancer

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APA (6th Edition):

Botham, R. C. (2016). Development of PAC-1 as a privileged agent for combination chemotherapy. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/92913

Chicago Manual of Style (16th Edition):

Botham, Rachel C. “Development of PAC-1 as a privileged agent for combination chemotherapy.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/92913.

MLA Handbook (7th Edition):

Botham, Rachel C. “Development of PAC-1 as a privileged agent for combination chemotherapy.” 2016. Web. 26 Aug 2019.

Vancouver:

Botham RC. Development of PAC-1 as a privileged agent for combination chemotherapy. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/92913.

Council of Science Editors:

Botham RC. Development of PAC-1 as a privileged agent for combination chemotherapy. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/92913


University of Illinois – Urbana-Champaign

27. Black Pyrkosz, Alexis A. Evolution and dynamic behavior of transfer RNA in the first two steps of translation.

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

 In protein synthesis, a key component of the cellular machinery is transfer RNA (tRNA). This small nucleic acid is crucial to the maintenance of the… (more)

Subjects/Keywords: transfer RNA; aminoacyl-tRNA synthetase; identity elements; bioinformatics; Shannon information entropy; molecular dynamics; dynamical networks; mmpbsa; free energies of binding; dissociation mechanism; molecular modeling; GluRS; CysRS

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APA (6th Edition):

Black Pyrkosz, A. A. (2010). Evolution and dynamic behavior of transfer RNA in the first two steps of translation. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/15505

Chicago Manual of Style (16th Edition):

Black Pyrkosz, Alexis A. “Evolution and dynamic behavior of transfer RNA in the first two steps of translation.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/15505.

MLA Handbook (7th Edition):

Black Pyrkosz, Alexis A. “Evolution and dynamic behavior of transfer RNA in the first two steps of translation.” 2010. Web. 26 Aug 2019.

Vancouver:

Black Pyrkosz AA. Evolution and dynamic behavior of transfer RNA in the first two steps of translation. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/15505.

Council of Science Editors:

Black Pyrkosz AA. Evolution and dynamic behavior of transfer RNA in the first two steps of translation. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/15505


University of Illinois – Urbana-Champaign

28. Palchaudhuri, Rahul. Development and Mechanistic Characterization of Novel Small Molecules as Cancer Therapeutics.

Degree: PhD, 0335, 2011, University of Illinois – Urbana-Champaign

 The discovery and development of novel small molecules as anti-cancer agents plays an integral role in the fight against cancer. Such efforts will lead to… (more)

Subjects/Keywords: Cancer; Therapeutic; Mechanism of action; Small Molecule

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APA (6th Edition):

Palchaudhuri, R. (2011). Development and Mechanistic Characterization of Novel Small Molecules as Cancer Therapeutics. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/26382

Chicago Manual of Style (16th Edition):

Palchaudhuri, Rahul. “Development and Mechanistic Characterization of Novel Small Molecules as Cancer Therapeutics.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/26382.

MLA Handbook (7th Edition):

Palchaudhuri, Rahul. “Development and Mechanistic Characterization of Novel Small Molecules as Cancer Therapeutics.” 2011. Web. 26 Aug 2019.

Vancouver:

Palchaudhuri R. Development and Mechanistic Characterization of Novel Small Molecules as Cancer Therapeutics. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/26382.

Council of Science Editors:

Palchaudhuri R. Development and Mechanistic Characterization of Novel Small Molecules as Cancer Therapeutics. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/26382


University of Illinois – Urbana-Champaign

29. Vincil, Gretchen. Design, synthesis and characterization of fluorescent hyperbranched polyglycerols and organic nanoparticles with covalently bound anti-fading agents.

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

 The photobleaching of fluorophores is a major limitation in fluorescence microscopy. We sought to create a brighter and more stable fluorophore by covalently attaching fluorescein… (more)

Subjects/Keywords: photobleaching; photostability; fluorescein; anti-fading agents; hyper-branched polymers

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APA (6th Edition):

Vincil, G. (2015). Design, synthesis and characterization of fluorescent hyperbranched polyglycerols and organic nanoparticles with covalently bound anti-fading agents. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/72771

Chicago Manual of Style (16th Edition):

Vincil, Gretchen. “Design, synthesis and characterization of fluorescent hyperbranched polyglycerols and organic nanoparticles with covalently bound anti-fading agents.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/72771.

MLA Handbook (7th Edition):

Vincil, Gretchen. “Design, synthesis and characterization of fluorescent hyperbranched polyglycerols and organic nanoparticles with covalently bound anti-fading agents.” 2015. Web. 26 Aug 2019.

Vancouver:

Vincil G. Design, synthesis and characterization of fluorescent hyperbranched polyglycerols and organic nanoparticles with covalently bound anti-fading agents. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/72771.

Council of Science Editors:

Vincil G. Design, synthesis and characterization of fluorescent hyperbranched polyglycerols and organic nanoparticles with covalently bound anti-fading agents. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/72771


University of Illinois – Urbana-Champaign

30. Zhao, Xi Ling. Discovery and structural characterization of lanthipeptides from soil and rumen bacteria.

Degree: PhD, Chemistry, 2017, University of Illinois – Urbana-Champaign

 As members of the ribosomally synthesized and post-translationally modified peptide natural products (RiPPs), lanthipeptides possess myriad structural diversity and potential for discovery using genome-guided approaches.… (more)

Subjects/Keywords: Ribosomally synthesized and post-translationally modified peptide natural products (RiPPs); Lanthipeptides; Heterologous expression of gene clusters; Combinatorial biosynthesis

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APA (6th Edition):

Zhao, X. L. (2017). Discovery and structural characterization of lanthipeptides from soil and rumen bacteria. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/97537

Chicago Manual of Style (16th Edition):

Zhao, Xi Ling. “Discovery and structural characterization of lanthipeptides from soil and rumen bacteria.” 2017. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 26, 2019. http://hdl.handle.net/2142/97537.

MLA Handbook (7th Edition):

Zhao, Xi Ling. “Discovery and structural characterization of lanthipeptides from soil and rumen bacteria.” 2017. Web. 26 Aug 2019.

Vancouver:

Zhao XL. Discovery and structural characterization of lanthipeptides from soil and rumen bacteria. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2017. [cited 2019 Aug 26]. Available from: http://hdl.handle.net/2142/97537.

Council of Science Editors:

Zhao XL. Discovery and structural characterization of lanthipeptides from soil and rumen bacteria. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2017. Available from: http://hdl.handle.net/2142/97537

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