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You searched for +publisher:"University of Illinois – Urbana-Champaign" +contributor:("Oldfield, Eric"). Showing records 1 – 23 of 23 total matches.

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University of Illinois – Urbana-Champaign

1. 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 December 03, 2020. 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. 03 Dec 2020.

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 2020 Dec 03]. 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

2. 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 December 03, 2020. http://hdl.handle.net/2142/45658.

MLA Handbook (7th Edition):

Zhu, Wei. “Targeting isoprenoid biosynthesis for drug discovery.” 2013. Web. 03 Dec 2020.

Vancouver:

Zhu W. Targeting isoprenoid biosynthesis for drug discovery. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2020 Dec 03]. 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

3. Guerra, Francisco. Investigating pathogen 4Fe-4S protein targets and cancer chemotherapies with bisphosphonate/diphosphate inhibitors.

Degree: PhD, 0319, 2015, University of Illinois – Urbana-Champaign

 The broad, long-term objective of this research is to develop drug leads for new antibiotics, antiparasitics, and cancer chemotherapeutics. Two main areas of focus are… (more)

Subjects/Keywords: isoprenoid; iron-sulfur proteins; 4Fe-4S; bisphosphonate; diphosphate

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APA (6th Edition):

Guerra, F. (2015). Investigating pathogen 4Fe-4S protein targets and cancer chemotherapies with bisphosphonate/diphosphate inhibitors. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/72983

Chicago Manual of Style (16th Edition):

Guerra, Francisco. “Investigating pathogen 4Fe-4S protein targets and cancer chemotherapies with bisphosphonate/diphosphate inhibitors.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 03, 2020. http://hdl.handle.net/2142/72983.

MLA Handbook (7th Edition):

Guerra, Francisco. “Investigating pathogen 4Fe-4S protein targets and cancer chemotherapies with bisphosphonate/diphosphate inhibitors.” 2015. Web. 03 Dec 2020.

Vancouver:

Guerra F. Investigating pathogen 4Fe-4S protein targets and cancer chemotherapies with bisphosphonate/diphosphate inhibitors. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/2142/72983.

Council of Science Editors:

Guerra F. Investigating pathogen 4Fe-4S protein targets and cancer chemotherapies with bisphosphonate/diphosphate inhibitors. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/72983


University of Illinois – Urbana-Champaign

4. Li, Jikun. Mechanism, inhibition and spectroscopy of isoprenoid biosynthesis enzymes.

Degree: PhD, 0319, 2014, University of Illinois – Urbana-Champaign

 Isoprenoids (or terpenes) are a large class of compounds with great physiological importance in all kingdoms of life. The research in this work explored the… (more)

Subjects/Keywords: isoprenoid biosynthesis; electron paramagnetic resonance (EPR) spectroscopy; drug discovery

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APA (6th Edition):

Li, J. (2014). Mechanism, inhibition and spectroscopy of isoprenoid biosynthesis enzymes. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/50443

Chicago Manual of Style (16th Edition):

Li, Jikun. “Mechanism, inhibition and spectroscopy of isoprenoid biosynthesis enzymes.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 03, 2020. http://hdl.handle.net/2142/50443.

MLA Handbook (7th Edition):

Li, Jikun. “Mechanism, inhibition and spectroscopy of isoprenoid biosynthesis enzymes.” 2014. Web. 03 Dec 2020.

Vancouver:

Li J. Mechanism, inhibition and spectroscopy of isoprenoid biosynthesis enzymes. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/2142/50443.

Council of Science Editors:

Li J. Mechanism, inhibition and spectroscopy of isoprenoid biosynthesis enzymes. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/50443


University of Illinois – Urbana-Champaign

5. Wang, Weixue. Mechanisms of action and inhibition of [4Fe-4S] proteins IspG and IspH in isoprenoid biosynthesis.

Degree: PhD, 0319, 2012, University of Illinois – Urbana-Champaign

 The methylerythritol phosphate pathway (also known as the non-mevalonate pathway) of isoprenoid biosynthesis is potentially an important anti-bacterial and anti-malarial drug target. However, the catalytic… (more)

Subjects/Keywords: non-mevalonate pathway; methylerythritol phosphate pathway; IspG; IspH; GcpE; LytB; iron-sulfur; 4Fe-4S; bioorganometallic; inhibition

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APA (6th Edition):

Wang, W. (2012). Mechanisms of action and inhibition of [4Fe-4S] proteins IspG and IspH in isoprenoid biosynthesis. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/31943

Chicago Manual of Style (16th Edition):

Wang, Weixue. “Mechanisms of action and inhibition of [4Fe-4S] proteins IspG and IspH in isoprenoid biosynthesis.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 03, 2020. http://hdl.handle.net/2142/31943.

MLA Handbook (7th Edition):

Wang, Weixue. “Mechanisms of action and inhibition of [4Fe-4S] proteins IspG and IspH in isoprenoid biosynthesis.” 2012. Web. 03 Dec 2020.

Vancouver:

Wang W. Mechanisms of action and inhibition of [4Fe-4S] proteins IspG and IspH in isoprenoid biosynthesis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/2142/31943.

Council of Science Editors:

Wang W. Mechanisms of action and inhibition of [4Fe-4S] proteins IspG and IspH in isoprenoid biosynthesis. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/31943


University of Illinois – Urbana-Champaign

6. Wang, Yang. Multi-target drug discovery against Staphylococcus aureus and Trypanosoma brucei infections.

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

 The drug resistance has become a big threat to human health, and there is currently a dearth of new antibiotics being introduced. In order to… (more)

Subjects/Keywords: undecaprenyl synthesis; Staphylococcus aureus; Trypanosoma brucei

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APA (6th Edition):

Wang, Y. (2016). Multi-target drug discovery against Staphylococcus aureus and Trypanosoma brucei infections. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/90768

Chicago Manual of Style (16th Edition):

Wang, Yang. “Multi-target drug discovery against Staphylococcus aureus and Trypanosoma brucei infections.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 03, 2020. http://hdl.handle.net/2142/90768.

MLA Handbook (7th Edition):

Wang, Yang. “Multi-target drug discovery against Staphylococcus aureus and Trypanosoma brucei infections.” 2016. Web. 03 Dec 2020.

Vancouver:

Wang Y. Multi-target drug discovery against Staphylococcus aureus and Trypanosoma brucei infections. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/2142/90768.

Council of Science Editors:

Wang Y. Multi-target drug discovery against Staphylococcus aureus and Trypanosoma brucei infections. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/90768


University of Illinois – Urbana-Champaign

7. Rao, Guodong. Structure and function of the terpene biosynthesis enzyme, IspH.

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

 The protein IspH, (E)-1-hydroxy-2-methyl-but-2-enyl 4-diphosphate reductase, is an essential enzyme in isoprenoid biosynthesis and an important drug/herbicide target. The main research in this work investigated… (more)

Subjects/Keywords: IspH; Iron-sulfur cluster; Infectious diseases; Metalloenzymes

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APA (6th Edition):

Rao, G. (2016). Structure and function of the terpene biosynthesis enzyme, IspH. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/93021

Chicago Manual of Style (16th Edition):

Rao, Guodong. “Structure and function of the terpene biosynthesis enzyme, IspH.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 03, 2020. http://hdl.handle.net/2142/93021.

MLA Handbook (7th Edition):

Rao, Guodong. “Structure and function of the terpene biosynthesis enzyme, IspH.” 2016. Web. 03 Dec 2020.

Vancouver:

Rao G. Structure and function of the terpene biosynthesis enzyme, IspH. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/2142/93021.

Council of Science Editors:

Rao G. Structure and function of the terpene biosynthesis enzyme, IspH. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/93021


University of Illinois – Urbana-Champaign

8. Desai, Janish. Targeting isoprenoid and quinone biosynthesis for antimicrobial discovery.

Degree: PhD, Biophysics & Computnl Biology, 2016, University of Illinois – Urbana-Champaign

 Enzymes in isoprenoid biosynthesis pathway play important roles in all living organisms. Here we report the first structure of heptaprenyl diphosphate synthase from Staphylococcus aureus… (more)

Subjects/Keywords: Drug Discovery; Protein chemistry; Protein-protein interactions; Isoprenoid biosyntheis; Quinone biosynthesis; Bisphosphonates; Cell wall biosynthesis

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APA (6th Edition):

Desai, J. (2016). Targeting isoprenoid and quinone biosynthesis for antimicrobial discovery. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95269

Chicago Manual of Style (16th Edition):

Desai, Janish. “Targeting isoprenoid and quinone biosynthesis for antimicrobial discovery.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 03, 2020. http://hdl.handle.net/2142/95269.

MLA Handbook (7th Edition):

Desai, Janish. “Targeting isoprenoid and quinone biosynthesis for antimicrobial discovery.” 2016. Web. 03 Dec 2020.

Vancouver:

Desai J. Targeting isoprenoid and quinone biosynthesis for antimicrobial discovery. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/2142/95269.

Council of Science Editors:

Desai J. Targeting isoprenoid and quinone biosynthesis for antimicrobial discovery. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95269


University of Illinois – Urbana-Champaign

9. 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 December 03, 2020. http://hdl.handle.net/2142/26307.

MLA Handbook (7th Edition):

No, Joo Hwan. “Drug discovery against malaria parasite: drug repositioning strategy.” 2011. Web. 03 Dec 2020.

Vancouver:

No JH. Drug discovery against malaria parasite: drug repositioning strategy. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2020 Dec 03]. 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

10. O'Dowd, Bing. ISPH fusion proteins, ISPH inhibition, and bisphosphonate mechanism of action.

Degree: PhD, Chemistry, 2018, University of Illinois – Urbana-Champaign

 In the first part of this work, IspH, (E)-1-hydroxy-2-methyl-but-2-enyl 4-diphosphate reductase was studied. In most bacteria, apicomplexan parasites, and plants, the biosynthesis of the five… (more)

Subjects/Keywords: IspH; bisphosphonates

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APA (6th Edition):

O'Dowd, B. (2018). ISPH fusion proteins, ISPH inhibition, and bisphosphonate mechanism of action. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/101638

Chicago Manual of Style (16th Edition):

O'Dowd, Bing. “ISPH fusion proteins, ISPH inhibition, and bisphosphonate mechanism of action.” 2018. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 03, 2020. http://hdl.handle.net/2142/101638.

MLA Handbook (7th Edition):

O'Dowd, Bing. “ISPH fusion proteins, ISPH inhibition, and bisphosphonate mechanism of action.” 2018. Web. 03 Dec 2020.

Vancouver:

O'Dowd B. ISPH fusion proteins, ISPH inhibition, and bisphosphonate mechanism of action. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2018. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/2142/101638.

Council of Science Editors:

O'Dowd B. ISPH fusion proteins, ISPH inhibition, and bisphosphonate mechanism of action. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2018. Available from: http://hdl.handle.net/2142/101638


University of Illinois – Urbana-Champaign

11. Ford, Courtney Lynn. Oxyanion reduction in a non-heme iron system.

Degree: PhD, Chemistry, 2018, University of Illinois – Urbana-Champaign

 The secondary coordination sphere of metalloenzymes is implicated in controlling nuclearity, enhancing substrate selectivity, and stabilizing reactive intermediates, and is thus essential in promoting the… (more)

Subjects/Keywords: oxyanion reduction; catalytic perchlorate reduction; halogen oxyanions; selenium oxyanions; secondary coordination sphere

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APA (6th Edition):

Ford, C. L. (2018). Oxyanion reduction in a non-heme iron system. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/101128

Chicago Manual of Style (16th Edition):

Ford, Courtney Lynn. “Oxyanion reduction in a non-heme iron system.” 2018. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 03, 2020. http://hdl.handle.net/2142/101128.

MLA Handbook (7th Edition):

Ford, Courtney Lynn. “Oxyanion reduction in a non-heme iron system.” 2018. Web. 03 Dec 2020.

Vancouver:

Ford CL. Oxyanion reduction in a non-heme iron system. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2018. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/2142/101128.

Council of Science Editors:

Ford CL. Oxyanion reduction in a non-heme iron system. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2018. Available from: http://hdl.handle.net/2142/101128


University of Illinois – Urbana-Champaign

12. 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 December 03, 2020. http://hdl.handle.net/2142/29545.

MLA Handbook (7th Edition):

Velasquez, Juan. “Biosynthesis of the antimicrobial peptide epilancin 15X.” 2012. Web. 03 Dec 2020.

Vancouver:

Velasquez J. Biosynthesis of the antimicrobial peptide epilancin 15X. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2020 Dec 03]. 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

13. Lemkau, Luisel. A comparison of resultant fibrils upon environmental and sequential manipulations of α-synuclein, a Parkinson’s disease associated protein.

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

 α-Synuclein (AS) fibrils are the main component of Lewy bodies, filamentous inclusions known as the pathological hallmark of Parkinson’s disease (PD). The normal function, toxic… (more)

Subjects/Keywords: solid-state-NMR; mutants; low pH; metals

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APA (6th Edition):

Lemkau, L. (2012). A comparison of resultant fibrils upon environmental and sequential manipulations of α-synuclein, a Parkinson’s disease associated protein. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/29574

Chicago Manual of Style (16th Edition):

Lemkau, Luisel. “A comparison of resultant fibrils upon environmental and sequential manipulations of α-synuclein, a Parkinson’s disease associated protein.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 03, 2020. http://hdl.handle.net/2142/29574.

MLA Handbook (7th Edition):

Lemkau, Luisel. “A comparison of resultant fibrils upon environmental and sequential manipulations of α-synuclein, a Parkinson’s disease associated protein.” 2012. Web. 03 Dec 2020.

Vancouver:

Lemkau L. A comparison of resultant fibrils upon environmental and sequential manipulations of α-synuclein, a Parkinson’s disease associated protein. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/2142/29574.

Council of Science Editors:

Lemkau L. A comparison of resultant fibrils upon environmental and sequential manipulations of α-synuclein, a Parkinson’s disease associated protein. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/29574


University of Illinois – Urbana-Champaign

14. Nguyen, Lien Thi Thuy. Design, synthesis, and biological activities of small molecules that target myotonic dystrophy.

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

 Myotonic dystrophy (DM) is a triple-repeat expansion, multi-systemic disease that affects one in eight thousand people worldwide. The cause of the disease is a progressive,… (more)

Subjects/Keywords: Myotonic Dystrophy; Drug development

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APA (6th Edition):

Nguyen, L. T. T. (2016). Design, synthesis, and biological activities of small molecules that target myotonic dystrophy. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/90730

Chicago Manual of Style (16th Edition):

Nguyen, Lien Thi Thuy. “Design, synthesis, and biological activities of small molecules that target myotonic dystrophy.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 03, 2020. http://hdl.handle.net/2142/90730.

MLA Handbook (7th Edition):

Nguyen, Lien Thi Thuy. “Design, synthesis, and biological activities of small molecules that target myotonic dystrophy.” 2016. Web. 03 Dec 2020.

Vancouver:

Nguyen LTT. Design, synthesis, and biological activities of small molecules that target myotonic dystrophy. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/2142/90730.

Council of Science Editors:

Nguyen LTT. Design, synthesis, and biological activities of small molecules that target myotonic dystrophy. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/90730


University of Illinois – Urbana-Champaign

15. Sperling, Lindsay J. Solid-state NMR studies of membrane proteins and membrane protein complexes.

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

 Membrane proteins help control nearly every process in the cell, which is why approximately 50% of pharmaceuticals currently on the market target membrane proteins. Knowledge… (more)

Subjects/Keywords: Cytochrome bo3 oxidase; DsbA/DsbB; Magic-angle Spinning; Membrane Proteins; Solid-state nuclear magnetic resonance (NMR)

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APA (6th Edition):

Sperling, L. J. (2011). Solid-state NMR studies of membrane proteins and membrane protein complexes. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/26275

Chicago Manual of Style (16th Edition):

Sperling, Lindsay J. “Solid-state NMR studies of membrane proteins and membrane protein complexes.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 03, 2020. http://hdl.handle.net/2142/26275.

MLA Handbook (7th Edition):

Sperling, Lindsay J. “Solid-state NMR studies of membrane proteins and membrane protein complexes.” 2011. Web. 03 Dec 2020.

Vancouver:

Sperling LJ. Solid-state NMR studies of membrane proteins and membrane protein complexes. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/2142/26275.

Council of Science Editors:

Sperling LJ. Solid-state NMR studies of membrane proteins and membrane protein complexes. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/26275


University of Illinois – Urbana-Champaign

16. Lencina, Andrea Mariana. Biochemical characterization of respiratory chain flavoproteins.

Degree: PhD, Biochemistry, 2018, University of Illinois – Urbana-Champaign

 Respiring organisms derive energy mainly from electron transfer reactions that are coupled to the translocation of ions across the cell membrane. This process is performed… (more)

Subjects/Keywords: flavoprotein; electron transport chain; nadh dehydrogenase; sulfide quinone reductase; coenzyme A disulfide reductase; Streptococcus agalactiae; Caldivirga maquilingensis; Thermus thermophilus

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APA (6th Edition):

Lencina, A. M. (2018). Biochemical characterization of respiratory chain flavoproteins. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/101797

Chicago Manual of Style (16th Edition):

Lencina, Andrea Mariana. “Biochemical characterization of respiratory chain flavoproteins.” 2018. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 03, 2020. http://hdl.handle.net/2142/101797.

MLA Handbook (7th Edition):

Lencina, Andrea Mariana. “Biochemical characterization of respiratory chain flavoproteins.” 2018. Web. 03 Dec 2020.

Vancouver:

Lencina AM. Biochemical characterization of respiratory chain flavoproteins. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2018. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/2142/101797.

Council of Science Editors:

Lencina AM. Biochemical characterization of respiratory chain flavoproteins. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2018. Available from: http://hdl.handle.net/2142/101797


University of Illinois – Urbana-Champaign

17. Schwalen, Christopher Joseph. Practical applications of genomics to natural product discovery and biosynthesis.

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

 Natural products, generally defined as metabolites of biotic origin, have a long history as medicines and have remained a fruitful source of new drug leads… (more)

Subjects/Keywords: Natural product; Biosynthesis; YcaO; Lasso peptide; Genomic

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APA (6th Edition):

Schwalen, C. J. (2017). Practical applications of genomics to natural product discovery and biosynthesis. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/99245

Chicago Manual of Style (16th Edition):

Schwalen, Christopher Joseph. “Practical applications of genomics to natural product discovery and biosynthesis.” 2017. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 03, 2020. http://hdl.handle.net/2142/99245.

MLA Handbook (7th Edition):

Schwalen, Christopher Joseph. “Practical applications of genomics to natural product discovery and biosynthesis.” 2017. Web. 03 Dec 2020.

Vancouver:

Schwalen CJ. Practical applications of genomics to natural product discovery and biosynthesis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2017. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/2142/99245.

Council of Science Editors:

Schwalen CJ. Practical applications of genomics to natural product discovery and biosynthesis. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2017. Available from: http://hdl.handle.net/2142/99245

18. Lin, Fu-Yang. Head-to-head terpene synthases: Mechanism of action and inhibition.

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

 ???Head-to-head??? terpene synthases catalyze the first committed steps in sterol and carotenoid biosynthesis: the condensation of two isoprenoid diphosphates to form cyclopropylcarbinyl diphosphates, followed by… (more)

Subjects/Keywords: terpenes; isoprenoids; antibiotics; virulence factor; dehydrosqualene synthase; Dehydrosqualene synthase (CrtM); squalene synthase (SQS); drug design; high throughput screening

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APA (6th Edition):

Lin, F. (2011). Head-to-head terpene synthases: Mechanism of action and inhibition. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/24489

Chicago Manual of Style (16th Edition):

Lin, Fu-Yang. “Head-to-head terpene synthases: Mechanism of action and inhibition.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 03, 2020. http://hdl.handle.net/2142/24489.

MLA Handbook (7th Edition):

Lin, Fu-Yang. “Head-to-head terpene synthases: Mechanism of action and inhibition.” 2011. Web. 03 Dec 2020.

Vancouver:

Lin F. Head-to-head terpene synthases: Mechanism of action and inhibition. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/2142/24489.

Council of Science Editors:

Lin F. Head-to-head terpene synthases: Mechanism of action and inhibition. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/24489

19. Feng, Xinxin. Mechanisms of bacterial polyprenyl transferases and multi-target drug discovery for tuberculosis.

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

 Bacterial polyprenyl transferases transfer polyprenyl groups onto molecular acceptors, such as proteins and small molecules, and they are very important functional entities that are involved… (more)

Subjects/Keywords: bacterial polyprenyl transferases; isoprenoid biosynthesis; terpene biosynthesis; drug discovery; infectious disease; tuberculosis

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APA (6th Edition):

Feng, X. (2014). Mechanisms of bacterial polyprenyl transferases and multi-target drug discovery for tuberculosis. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/49419

Chicago Manual of Style (16th Edition):

Feng, Xinxin. “Mechanisms of bacterial polyprenyl transferases and multi-target drug discovery for tuberculosis.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 03, 2020. http://hdl.handle.net/2142/49419.

MLA Handbook (7th Edition):

Feng, Xinxin. “Mechanisms of bacterial polyprenyl transferases and multi-target drug discovery for tuberculosis.” 2014. Web. 03 Dec 2020.

Vancouver:

Feng X. Mechanisms of bacterial polyprenyl transferases and multi-target drug discovery for tuberculosis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/2142/49419.

Council of Science Editors:

Feng X. Mechanisms of bacterial polyprenyl transferases and multi-target drug discovery for tuberculosis. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/49419

20. Nieuwkoop, Andrew. Structure determination of proteins and protein aggregates by magic-angle spinning solid-state NMR.

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

 Solid state NMR (SSNMR) is a structure determination technique uniquely suited to study protein aggregates and fibrils. Unlike solution NMR or X-ray crystallography, SSNMR can… (more)

Subjects/Keywords: Solid-state NMR; protein structure determination; fibrils; GB1; alpha synuclein; Parkinson’s disease; TEDOR; proton detection; nuclear magnetic resonance (NMR)

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APA (6th Edition):

Nieuwkoop, A. (2012). Structure determination of proteins and protein aggregates by magic-angle spinning solid-state NMR. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/29544

Chicago Manual of Style (16th Edition):

Nieuwkoop, Andrew. “Structure determination of proteins and protein aggregates by magic-angle spinning solid-state NMR.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 03, 2020. http://hdl.handle.net/2142/29544.

MLA Handbook (7th Edition):

Nieuwkoop, Andrew. “Structure determination of proteins and protein aggregates by magic-angle spinning solid-state NMR.” 2012. Web. 03 Dec 2020.

Vancouver:

Nieuwkoop A. Structure determination of proteins and protein aggregates by magic-angle spinning solid-state NMR. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/2142/29544.

Council of Science Editors:

Nieuwkoop A. Structure determination of proteins and protein aggregates by magic-angle spinning solid-state NMR. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/29544

21. Finch, Kristin E. The discovery of small molecule inhibitors of poly(ADP-ribose) mediated cell death.

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

 The emergence of resistance to cancer treatments through methods that generate cell death by inducing DNA damage, such as chemotherapeutics and radiation therapy, is a… (more)

Subjects/Keywords: poly(ADP-ribose) glycohydrolase (PARG); Poly(ADP-ribose) polymerase (PARP); poly(ADP-ribose) (PAR); Rhodanines; small molecule inhibitors

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APA (6th Edition):

Finch, K. E. (2011). The discovery of small molecule inhibitors of poly(ADP-ribose) mediated cell death. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/24355

Chicago Manual of Style (16th Edition):

Finch, Kristin E. “The discovery of small molecule inhibitors of poly(ADP-ribose) mediated cell death.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 03, 2020. http://hdl.handle.net/2142/24355.

MLA Handbook (7th Edition):

Finch, Kristin E. “The discovery of small molecule inhibitors of poly(ADP-ribose) mediated cell death.” 2011. Web. 03 Dec 2020.

Vancouver:

Finch KE. The discovery of small molecule inhibitors of poly(ADP-ribose) mediated cell death. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/2142/24355.

Council of Science Editors:

Finch KE. The discovery of small molecule inhibitors of poly(ADP-ribose) mediated cell death. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/24355

22. Clay, Mary. Structural studies of membrane-associated complexes by solid-state NMR.

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

 The plasma membrane is one of the most important barriers in the human body. The membrane is far more than an inert platform supporting membrane… (more)

Subjects/Keywords: solid-state nuclear magnetic resonance (NMR); Amphotericin B; Ergosterol; phosphatidylserine; blood clotting

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APA (6th Edition):

Clay, M. (2015). Structural studies of membrane-associated complexes by solid-state NMR. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/72798

Chicago Manual of Style (16th Edition):

Clay, Mary. “Structural studies of membrane-associated complexes by solid-state NMR.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 03, 2020. http://hdl.handle.net/2142/72798.

MLA Handbook (7th Edition):

Clay, Mary. “Structural studies of membrane-associated complexes by solid-state NMR.” 2015. Web. 03 Dec 2020.

Vancouver:

Clay M. Structural studies of membrane-associated complexes by solid-state NMR. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/2142/72798.

Council of Science Editors:

Clay M. Structural studies of membrane-associated complexes by solid-state NMR. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/72798

23. Courtney, Joseph M. Automated protein NMR data analysis and its application to a-synuclein fibrils.

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

 In principle, nuclear magnetic resonance (NMR) spectroscopy provides structural and conformational information with sub-Angstrom precision and the ability to measure dynamics with timescales ranging from… (more)

Subjects/Keywords: Solid-state nuclear magnetic resonance (SSNMR); Alpha-synuclein; Magic-angle spinning (MAS)

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APA (6th Edition):

Courtney, J. M. (2017). Automated protein NMR data analysis and its application to a-synuclein fibrils. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/97595

Chicago Manual of Style (16th Edition):

Courtney, Joseph M. “Automated protein NMR data analysis and its application to a-synuclein fibrils.” 2017. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 03, 2020. http://hdl.handle.net/2142/97595.

MLA Handbook (7th Edition):

Courtney, Joseph M. “Automated protein NMR data analysis and its application to a-synuclein fibrils.” 2017. Web. 03 Dec 2020.

Vancouver:

Courtney JM. Automated protein NMR data analysis and its application to a-synuclein fibrils. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2017. [cited 2020 Dec 03]. Available from: http://hdl.handle.net/2142/97595.

Council of Science Editors:

Courtney JM. Automated protein NMR data analysis and its application to a-synuclein fibrils. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2017. Available from: http://hdl.handle.net/2142/97595

.