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You searched for +publisher:"University of Michigan" +contributor:("Marsh, E Neil G"). Showing records 1 – 30 of 31 total matches.

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University of Michigan

1. Chen, Junjie. Aggregation and Dendrimer Mediated Secondary Binding towards Folate Binding Protein & Fatigue Failure Mechanism of Anterior Cruciate Ligament Fracture.

Degree: PhD, Chemistry, 2018, University of Michigan

 Drug conjugation gives many advantages such as improved targeting, solubility and retention. How conjugated drugs interact with proteins is a key question to answer in… (more)

Subjects/Keywords: dendrimer drug delivery; anterior cruciate ligament injury; nanoparticle aggregation; Chemistry; Science

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APA (6th Edition):

Chen, J. (2018). Aggregation and Dendrimer Mediated Secondary Binding towards Folate Binding Protein & Fatigue Failure Mechanism of Anterior Cruciate Ligament Fracture. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/144055

Chicago Manual of Style (16th Edition):

Chen, Junjie. “Aggregation and Dendrimer Mediated Secondary Binding towards Folate Binding Protein & Fatigue Failure Mechanism of Anterior Cruciate Ligament Fracture.” 2018. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/144055.

MLA Handbook (7th Edition):

Chen, Junjie. “Aggregation and Dendrimer Mediated Secondary Binding towards Folate Binding Protein & Fatigue Failure Mechanism of Anterior Cruciate Ligament Fracture.” 2018. Web. 26 Jun 2019.

Vancouver:

Chen J. Aggregation and Dendrimer Mediated Secondary Binding towards Folate Binding Protein & Fatigue Failure Mechanism of Anterior Cruciate Ligament Fracture. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/144055.

Council of Science Editors:

Chen J. Aggregation and Dendrimer Mediated Secondary Binding towards Folate Binding Protein & Fatigue Failure Mechanism of Anterior Cruciate Ligament Fracture. [Doctoral Dissertation]. University of Michigan; 2018. Available from: http://hdl.handle.net/2027.42/144055


University of Michigan

2. Liu, Yuwei. Surface Studies on the Structure and Functionality of Bioactive Materials.

Degree: PhD, Chemistry, 2014, University of Michigan

 Bioactive materials are critical in many applications in the fields ranging from antibiofouling coatings to tissue engineering to biosensing devices. The construction of bioactive materials… (more)

Subjects/Keywords: Surface Analysis; Sum Frequency Generation; Antibiofouling Coatings; Antimicrobial Peptide Immobilization; Enzyme Immobilization; Structure-activity Relationship; Chemistry; Science

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APA (6th Edition):

Liu, Y. (2014). Surface Studies on the Structure and Functionality of Bioactive Materials. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/109042

Chicago Manual of Style (16th Edition):

Liu, Yuwei. “Surface Studies on the Structure and Functionality of Bioactive Materials.” 2014. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/109042.

MLA Handbook (7th Edition):

Liu, Yuwei. “Surface Studies on the Structure and Functionality of Bioactive Materials.” 2014. Web. 26 Jun 2019.

Vancouver:

Liu Y. Surface Studies on the Structure and Functionality of Bioactive Materials. [Internet] [Doctoral dissertation]. University of Michigan; 2014. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/109042.

Council of Science Editors:

Liu Y. Surface Studies on the Structure and Functionality of Bioactive Materials. [Doctoral Dissertation]. University of Michigan; 2014. Available from: http://hdl.handle.net/2027.42/109042

3. Ogorzalek, Tadeusz L. Examining the Behavior of Surface Tethered Enzymes.

Degree: PhD, Chemical Biology, 2015, University of Michigan

 Surface-immobilized enzymes are important for a wide range of technological applications, including industrial catalysis, drug delivery, medical diagnosis and biosensors. However, our understanding of how… (more)

Subjects/Keywords: Enzyme Immobilization; Surface Attachment; Biological Chemistry; Science

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APA (6th Edition):

Ogorzalek, T. L. (2015). Examining the Behavior of Surface Tethered Enzymes. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/111541

Chicago Manual of Style (16th Edition):

Ogorzalek, Tadeusz L. “Examining the Behavior of Surface Tethered Enzymes.” 2015. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/111541.

MLA Handbook (7th Edition):

Ogorzalek, Tadeusz L. “Examining the Behavior of Surface Tethered Enzymes.” 2015. Web. 26 Jun 2019.

Vancouver:

Ogorzalek TL. Examining the Behavior of Surface Tethered Enzymes. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/111541.

Council of Science Editors:

Ogorzalek TL. Examining the Behavior of Surface Tethered Enzymes. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/111541


University of Michigan

4. Bruno, Paul Anthony. Developing Proteomimetic Inhibitors of Large Surface Area, Low Affinity Protein-Protein Interaction.

Degree: PhD, Chemistry, 2015, University of Michigan

 The majority of cellular processes are governed by the activity of multimeric protein complexes assembled through specific protein-protein interactions (PPIs). With more than 650,000 estimated… (more)

Subjects/Keywords: Protein-protein interactions; Chemical biology; Combination approaches; Stabilized peptides; High-throughput screening; Transcription; Chemistry; Science

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APA (6th Edition):

Bruno, P. A. (2015). Developing Proteomimetic Inhibitors of Large Surface Area, Low Affinity Protein-Protein Interaction. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/113445

Chicago Manual of Style (16th Edition):

Bruno, Paul Anthony. “Developing Proteomimetic Inhibitors of Large Surface Area, Low Affinity Protein-Protein Interaction.” 2015. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/113445.

MLA Handbook (7th Edition):

Bruno, Paul Anthony. “Developing Proteomimetic Inhibitors of Large Surface Area, Low Affinity Protein-Protein Interaction.” 2015. Web. 26 Jun 2019.

Vancouver:

Bruno PA. Developing Proteomimetic Inhibitors of Large Surface Area, Low Affinity Protein-Protein Interaction. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/113445.

Council of Science Editors:

Bruno PA. Developing Proteomimetic Inhibitors of Large Surface Area, Low Affinity Protein-Protein Interaction. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/113445


University of Michigan

5. Phadke, Sameer D. Chemical Modulation of Phospho-Signaling Pathways Involved in Cancer.

Degree: PhD, Chemistry, 2015, University of Michigan

 Advancements in our understanding of the molecular causes of cancer have led to the therapeutic targeting of key enzymes involved in cell growth. Kinase inhibitors… (more)

Subjects/Keywords: kinase; chronic myelogenous leukemia; targeted therapy; Grb2; fragment screening; signaling pathways; Biological Chemistry; Oncology and Hematology; Chemistry; Health Sciences; Science

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APA (6th Edition):

Phadke, S. D. (2015). Chemical Modulation of Phospho-Signaling Pathways Involved in Cancer. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/113580

Chicago Manual of Style (16th Edition):

Phadke, Sameer D. “Chemical Modulation of Phospho-Signaling Pathways Involved in Cancer.” 2015. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/113580.

MLA Handbook (7th Edition):

Phadke, Sameer D. “Chemical Modulation of Phospho-Signaling Pathways Involved in Cancer.” 2015. Web. 26 Jun 2019.

Vancouver:

Phadke SD. Chemical Modulation of Phospho-Signaling Pathways Involved in Cancer. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/113580.

Council of Science Editors:

Phadke SD. Chemical Modulation of Phospho-Signaling Pathways Involved in Cancer. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/113580


University of Michigan

6. Waugh, Matthew William. Molecules to Burn: A Mechanistic Characterization of Cyanobacterial Aldehyde Deformylating Oxygenase.

Degree: PhD, Chemical Biology, 2015, University of Michigan

 The development of hydrocarbon based biofuels that can replace fossil fuels is essential to address the challenge of energy sustainability. However, there are few known… (more)

Subjects/Keywords: Biofuels; Non-Heme Iron Oxygenase; Aldehyde Decarbonylase; Protein Film Voltammetry; Solvent Isotope Effects; Enzyme Kinetics; Biological Chemistry; Science

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APA (6th Edition):

Waugh, M. W. (2015). Molecules to Burn: A Mechanistic Characterization of Cyanobacterial Aldehyde Deformylating Oxygenase. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/113585

Chicago Manual of Style (16th Edition):

Waugh, Matthew William. “Molecules to Burn: A Mechanistic Characterization of Cyanobacterial Aldehyde Deformylating Oxygenase.” 2015. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/113585.

MLA Handbook (7th Edition):

Waugh, Matthew William. “Molecules to Burn: A Mechanistic Characterization of Cyanobacterial Aldehyde Deformylating Oxygenase.” 2015. Web. 26 Jun 2019.

Vancouver:

Waugh MW. Molecules to Burn: A Mechanistic Characterization of Cyanobacterial Aldehyde Deformylating Oxygenase. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/113585.

Council of Science Editors:

Waugh MW. Molecules to Burn: A Mechanistic Characterization of Cyanobacterial Aldehyde Deformylating Oxygenase. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/113585


University of Michigan

7. Schroeder, McKenna. Immobilized Enzymes: Activity, Orientation, and Stability.

Degree: PhD, Chemical Biology, 2016, University of Michigan

 Enzyme immobilization is an important tool for many industrial and medical fields applications as well as biosensors. Much work has been done developing types of… (more)

Subjects/Keywords: Immobilized enzymes; Nitroreductase; Self-assembling monolayers; Enzyme kinetics; Enzyme stability; Enzyme orientation; Biological Chemistry; Science

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APA (6th Edition):

Schroeder, M. (2016). Immobilized Enzymes: Activity, Orientation, and Stability. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/135760

Chicago Manual of Style (16th Edition):

Schroeder, McKenna. “Immobilized Enzymes: Activity, Orientation, and Stability.” 2016. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/135760.

MLA Handbook (7th Edition):

Schroeder, McKenna. “Immobilized Enzymes: Activity, Orientation, and Stability.” 2016. Web. 26 Jun 2019.

Vancouver:

Schroeder M. Immobilized Enzymes: Activity, Orientation, and Stability. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/135760.

Council of Science Editors:

Schroeder M. Immobilized Enzymes: Activity, Orientation, and Stability. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/135760


University of Michigan

8. Patterson, Dustin P. Symmetry Assembled Supramolecular Protein Cages: Investigating a Strategy for Constructing New Biomaterials.

Degree: PhD, Chemistry, 2011, University of Michigan

 In nature, the assembly of individual protein subunits into larger quaternary structures allows new biological properties to emerge as consequence of the higher order structure.… (more)

Subjects/Keywords: Protein Assembly; De Novo Design; Directed Assembly; Supramolecular; Biological Chemistry; Chemistry; Science

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APA (6th Edition):

Patterson, D. P. (2011). Symmetry Assembled Supramolecular Protein Cages: Investigating a Strategy for Constructing New Biomaterials. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/84595

Chicago Manual of Style (16th Edition):

Patterson, Dustin P. “Symmetry Assembled Supramolecular Protein Cages: Investigating a Strategy for Constructing New Biomaterials.” 2011. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/84595.

MLA Handbook (7th Edition):

Patterson, Dustin P. “Symmetry Assembled Supramolecular Protein Cages: Investigating a Strategy for Constructing New Biomaterials.” 2011. Web. 26 Jun 2019.

Vancouver:

Patterson DP. Symmetry Assembled Supramolecular Protein Cages: Investigating a Strategy for Constructing New Biomaterials. [Internet] [Doctoral dissertation]. University of Michigan; 2011. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/84595.

Council of Science Editors:

Patterson DP. Symmetry Assembled Supramolecular Protein Cages: Investigating a Strategy for Constructing New Biomaterials. [Doctoral Dissertation]. University of Michigan; 2011. Available from: http://hdl.handle.net/2027.42/84595


University of Michigan

9. Bhave, Devayani P. Reducing the Mysteries of Sulfur Metabolism in Mycobacterium Tuberculosis.

Degree: PhD, Chemical Biology, 2011, University of Michigan

 Sulfur metabolic pathways are fundamental for survival and the expression of virulence in many pathogenic bacteria, including Mycobacterium tuberculosis. In addition, microbial sulfur metabolic pathways… (more)

Subjects/Keywords: Sulfur Metabolism in Mycobacterium Tuberculosis; Sulfate Assimilation Pathway; Adenosine-5'-Phosphosulfate Reductase; Iron-Sulfur Protein; Iron-sulfur Cluster; 3'-Phosphoadenosine-5'-Phosphosulfate Reductase; Biological Chemistry; Science

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APA (6th Edition):

Bhave, D. P. (2011). Reducing the Mysteries of Sulfur Metabolism in Mycobacterium Tuberculosis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/89843

Chicago Manual of Style (16th Edition):

Bhave, Devayani P. “Reducing the Mysteries of Sulfur Metabolism in Mycobacterium Tuberculosis.” 2011. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/89843.

MLA Handbook (7th Edition):

Bhave, Devayani P. “Reducing the Mysteries of Sulfur Metabolism in Mycobacterium Tuberculosis.” 2011. Web. 26 Jun 2019.

Vancouver:

Bhave DP. Reducing the Mysteries of Sulfur Metabolism in Mycobacterium Tuberculosis. [Internet] [Doctoral dissertation]. University of Michigan; 2011. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/89843.

Council of Science Editors:

Bhave DP. Reducing the Mysteries of Sulfur Metabolism in Mycobacterium Tuberculosis. [Doctoral Dissertation]. University of Michigan; 2011. Available from: http://hdl.handle.net/2027.42/89843


University of Michigan

10. Ellington, Benjamin Rex. Probing the Mechanisms of Aldehyde Decarbonylation Using Radical Clock Substrate Analogues.

Degree: PhD, Biological Chemistry, 2016, University of Michigan

 Global warming has led to increasing research into environmentally-friendly energy sources. One of the greatest sources of greenhouse gases is consumption of fossil fuels to… (more)

Subjects/Keywords: Radical Clock; Aldehyde Decarbonylation; Biofuel; Biological Chemistry; Science

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APA (6th Edition):

Ellington, B. R. (2016). Probing the Mechanisms of Aldehyde Decarbonylation Using Radical Clock Substrate Analogues. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/120649

Chicago Manual of Style (16th Edition):

Ellington, Benjamin Rex. “Probing the Mechanisms of Aldehyde Decarbonylation Using Radical Clock Substrate Analogues.” 2016. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/120649.

MLA Handbook (7th Edition):

Ellington, Benjamin Rex. “Probing the Mechanisms of Aldehyde Decarbonylation Using Radical Clock Substrate Analogues.” 2016. Web. 26 Jun 2019.

Vancouver:

Ellington BR. Probing the Mechanisms of Aldehyde Decarbonylation Using Radical Clock Substrate Analogues. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/120649.

Council of Science Editors:

Ellington BR. Probing the Mechanisms of Aldehyde Decarbonylation Using Radical Clock Substrate Analogues. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/120649


University of Michigan

11. Sciore, Aaron. A General, Symmetry-Based Approach for the Assembly of Proteins into Nanoscale Polyhedra.

Degree: PhD, Chemistry, 2016, University of Michigan

 The assembly of individual protein subunits into large-scale symmetrical structures is widespread in Nature and confers unique biological properties which have potential applications in nano-technology… (more)

Subjects/Keywords: protein self-assembly; Chemistry; Science

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APA (6th Edition):

Sciore, A. (2016). A General, Symmetry-Based Approach for the Assembly of Proteins into Nanoscale Polyhedra. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/120840

Chicago Manual of Style (16th Edition):

Sciore, Aaron. “A General, Symmetry-Based Approach for the Assembly of Proteins into Nanoscale Polyhedra.” 2016. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/120840.

MLA Handbook (7th Edition):

Sciore, Aaron. “A General, Symmetry-Based Approach for the Assembly of Proteins into Nanoscale Polyhedra.” 2016. Web. 26 Jun 2019.

Vancouver:

Sciore A. A General, Symmetry-Based Approach for the Assembly of Proteins into Nanoscale Polyhedra. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/120840.

Council of Science Editors:

Sciore A. A General, Symmetry-Based Approach for the Assembly of Proteins into Nanoscale Polyhedra. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/120840


University of Michigan

12. Das, Debasis. Mechanistic Studies on Aldehyde Decarbonylase from Cyanobacteria: A New Enzyme for Alkane Biosynthesis.

Degree: PhD, Chemistry, 2014, University of Michigan

 The challenge posed by global warming has sparked great interest in the development of new, green biofuels. Existing biofuels such as ethanol and biodiesel suffer… (more)

Subjects/Keywords: Aldehyde Decarbonylase; Chemistry; Science

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APA (6th Edition):

Das, D. (2014). Mechanistic Studies on Aldehyde Decarbonylase from Cyanobacteria: A New Enzyme for Alkane Biosynthesis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/107315

Chicago Manual of Style (16th Edition):

Das, Debasis. “Mechanistic Studies on Aldehyde Decarbonylase from Cyanobacteria: A New Enzyme for Alkane Biosynthesis.” 2014. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/107315.

MLA Handbook (7th Edition):

Das, Debasis. “Mechanistic Studies on Aldehyde Decarbonylase from Cyanobacteria: A New Enzyme for Alkane Biosynthesis.” 2014. Web. 26 Jun 2019.

Vancouver:

Das D. Mechanistic Studies on Aldehyde Decarbonylase from Cyanobacteria: A New Enzyme for Alkane Biosynthesis. [Internet] [Doctoral dissertation]. University of Michigan; 2014. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/107315.

Council of Science Editors:

Das D. Mechanistic Studies on Aldehyde Decarbonylase from Cyanobacteria: A New Enzyme for Alkane Biosynthesis. [Doctoral Dissertation]. University of Michigan; 2014. Available from: http://hdl.handle.net/2027.42/107315


University of Michigan

13. Conrad, John A. The Reactions of Flavin-Dependent Thymidylate Synthase from Thermotoga Maritima.

Degree: PhD, Chemical Biology, 2011, University of Michigan

 For decades the biosynthesis of thymidylate was thought to be catalyzed solely by thymidylate synthase. Recently a structurally unrelated new class of thymidylate synthase, ThyX,… (more)

Subjects/Keywords: Flavin; Enzymology; Oxidative Half-reaction; Reductive Half – Reaction; Biological Chemistry; Science

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APA (6th Edition):

Conrad, J. A. (2011). The Reactions of Flavin-Dependent Thymidylate Synthase from Thermotoga Maritima. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/86346

Chicago Manual of Style (16th Edition):

Conrad, John A. “The Reactions of Flavin-Dependent Thymidylate Synthase from Thermotoga Maritima.” 2011. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/86346.

MLA Handbook (7th Edition):

Conrad, John A. “The Reactions of Flavin-Dependent Thymidylate Synthase from Thermotoga Maritima.” 2011. Web. 26 Jun 2019.

Vancouver:

Conrad JA. The Reactions of Flavin-Dependent Thymidylate Synthase from Thermotoga Maritima. [Internet] [Doctoral dissertation]. University of Michigan; 2011. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/86346.

Council of Science Editors:

Conrad JA. The Reactions of Flavin-Dependent Thymidylate Synthase from Thermotoga Maritima. [Doctoral Dissertation]. University of Michigan; 2011. Available from: http://hdl.handle.net/2027.42/86346

14. Bennion, Jonathan. Multicomponent Crystallization of Energetic Materials.

Degree: PhD, Chemistry, 2017, University of Michigan

 Multicomponent crystallization (cocrystallization and solvate formation) offers the unique ability to post-synthetically alter the properties of a materials through noncovalent interactions between two or more… (more)

Subjects/Keywords: Multicomponent Crystallization; Energetic; Detonation; Cocrystal; Solvate; Sensitivity; Chemistry; Science

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APA (6th Edition):

Bennion, J. (2017). Multicomponent Crystallization of Energetic Materials. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/137056

Chicago Manual of Style (16th Edition):

Bennion, Jonathan. “Multicomponent Crystallization of Energetic Materials.” 2017. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/137056.

MLA Handbook (7th Edition):

Bennion, Jonathan. “Multicomponent Crystallization of Energetic Materials.” 2017. Web. 26 Jun 2019.

Vancouver:

Bennion J. Multicomponent Crystallization of Energetic Materials. [Internet] [Doctoral dissertation]. University of Michigan; 2017. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/137056.

Council of Science Editors:

Bennion J. Multicomponent Crystallization of Energetic Materials. [Doctoral Dissertation]. University of Michigan; 2017. Available from: http://hdl.handle.net/2027.42/137056

15. Wu, Biyun. Development of Hemocompatible Polymeric Materials for Blood-Contacting Medical Devices.

Degree: PhD, Chemistry, 2009, University of Michigan

 The research in this dissertation focuses on the development of novel multifunctional polymeric coatings that incorporate multiple antithrombogenic and/or anti-proliferative bioactive agents. The incorporated bioactive… (more)

Subjects/Keywords: Hemocompatibility; Polymer; Nitric Oxide; Cardiovascular; Blood; Coating; Chemistry; Science

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APA (6th Edition):

Wu, B. (2009). Development of Hemocompatible Polymeric Materials for Blood-Contacting Medical Devices. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/64718

Chicago Manual of Style (16th Edition):

Wu, Biyun. “Development of Hemocompatible Polymeric Materials for Blood-Contacting Medical Devices.” 2009. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/64718.

MLA Handbook (7th Edition):

Wu, Biyun. “Development of Hemocompatible Polymeric Materials for Blood-Contacting Medical Devices.” 2009. Web. 26 Jun 2019.

Vancouver:

Wu B. Development of Hemocompatible Polymeric Materials for Blood-Contacting Medical Devices. [Internet] [Doctoral dissertation]. University of Michigan; 2009. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/64718.

Council of Science Editors:

Wu B. Development of Hemocompatible Polymeric Materials for Blood-Contacting Medical Devices. [Doctoral Dissertation]. University of Michigan; 2009. Available from: http://hdl.handle.net/2027.42/64718

16. Taylor, Christopher. I. The Utility of Activation Domain Mimics as Targeted Inhibitors of Transcription II. The Design and Implementation of a Peer-Lead Module in Practical Research Ethics.

Degree: PhD, Chemistry, 2011, University of Michigan

 Because of the central role that transcription plays in regulating cell function and fate, the ability to cause a targeted increase or decrease in particular… (more)

Subjects/Keywords: Inhibitors of Protein-Protein Interactions; Synergy; Chemical Education; Cancer; Chemistry; Science

…the technical definition of misconduct, took place at the University of Michigan.22 In this… 

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APA (6th Edition):

Taylor, C. (2011). I. The Utility of Activation Domain Mimics as Targeted Inhibitors of Transcription II. The Design and Implementation of a Peer-Lead Module in Practical Research Ethics. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/89817

Chicago Manual of Style (16th Edition):

Taylor, Christopher. “I. The Utility of Activation Domain Mimics as Targeted Inhibitors of Transcription II. The Design and Implementation of a Peer-Lead Module in Practical Research Ethics.” 2011. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/89817.

MLA Handbook (7th Edition):

Taylor, Christopher. “I. The Utility of Activation Domain Mimics as Targeted Inhibitors of Transcription II. The Design and Implementation of a Peer-Lead Module in Practical Research Ethics.” 2011. Web. 26 Jun 2019.

Vancouver:

Taylor C. I. The Utility of Activation Domain Mimics as Targeted Inhibitors of Transcription II. The Design and Implementation of a Peer-Lead Module in Practical Research Ethics. [Internet] [Doctoral dissertation]. University of Michigan; 2011. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/89817.

Council of Science Editors:

Taylor C. I. The Utility of Activation Domain Mimics as Targeted Inhibitors of Transcription II. The Design and Implementation of a Peer-Lead Module in Practical Research Ethics. [Doctoral Dissertation]. University of Michigan; 2011. Available from: http://hdl.handle.net/2027.42/89817

17. Wands, Amberlyn M. Characterization of the Dynamic Interactions of Transcriptional Activators.

Degree: PhD, Chemistry, 2010, University of Michigan

 Transcription is initiated through a series of coupled binding equilibria between transcriptional activators and their array of protein targets within the transcriptional machinery. However, previous… (more)

Subjects/Keywords: Transcription; Transcriptional Activation; Transcriptional Activator; Transient Kinetics; Biological Chemistry; Chemistry; Science (General); Science

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APA (6th Edition):

Wands, A. M. (2010). Characterization of the Dynamic Interactions of Transcriptional Activators. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/77780

Chicago Manual of Style (16th Edition):

Wands, Amberlyn M. “Characterization of the Dynamic Interactions of Transcriptional Activators.” 2010. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/77780.

MLA Handbook (7th Edition):

Wands, Amberlyn M. “Characterization of the Dynamic Interactions of Transcriptional Activators.” 2010. Web. 26 Jun 2019.

Vancouver:

Wands AM. Characterization of the Dynamic Interactions of Transcriptional Activators. [Internet] [Doctoral dissertation]. University of Michigan; 2010. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/77780.

Council of Science Editors:

Wands AM. Characterization of the Dynamic Interactions of Transcriptional Activators. [Doctoral Dissertation]. University of Michigan; 2010. Available from: http://hdl.handle.net/2027.42/77780

18. Suzuki, Yuta. Fluorine NMR Studies on the Dynamics and Structure of Biologically Active Peptides.

Degree: PhD, Chemistry, 2013, University of Michigan

 Fluorine NMR is an excellent technique for studying changes in chemical environments due to its high sensitivity and large chemical shift dispersion. Since fluorine is… (more)

Subjects/Keywords: Fluorine NMR; Antimicrobial Peptide; Islet Amyloid Polypeptide; Amyloid Beta; Chemistry; Science

…Biophysics, University of Michigan, Ann Arbor, MI 4 810 9-1055, U S A. E-mail: [email protected]… 

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APA (6th Edition):

Suzuki, Y. (2013). Fluorine NMR Studies on the Dynamics and Structure of Biologically Active Peptides. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/98030

Chicago Manual of Style (16th Edition):

Suzuki, Yuta. “Fluorine NMR Studies on the Dynamics and Structure of Biologically Active Peptides.” 2013. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/98030.

MLA Handbook (7th Edition):

Suzuki, Yuta. “Fluorine NMR Studies on the Dynamics and Structure of Biologically Active Peptides.” 2013. Web. 26 Jun 2019.

Vancouver:

Suzuki Y. Fluorine NMR Studies on the Dynamics and Structure of Biologically Active Peptides. [Internet] [Doctoral dissertation]. University of Michigan; 2013. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/98030.

Council of Science Editors:

Suzuki Y. Fluorine NMR Studies on the Dynamics and Structure of Biologically Active Peptides. [Doctoral Dissertation]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/98030

19. Santos, Shana Marie. Understanding the Enzyme-inhibitor Interaction within the Substrate Pocket of Protein Tyrosine Kinases.

Degree: PhD, Chemistry, 2013, University of Michigan

 Protein phosphorylation occurs through enzymatic transfer of the gamma-phosphate of adenosine triphosphate (ATP) to the hydroxyl moieties of the amino acid residues serine, threonine, and… (more)

Subjects/Keywords: Substrate-competitive Kinase Inhibitors; Protein Tyrosine Kinases; Chemistry; Science

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APA (6th Edition):

Santos, S. M. (2013). Understanding the Enzyme-inhibitor Interaction within the Substrate Pocket of Protein Tyrosine Kinases. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/99913

Chicago Manual of Style (16th Edition):

Santos, Shana Marie. “Understanding the Enzyme-inhibitor Interaction within the Substrate Pocket of Protein Tyrosine Kinases.” 2013. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/99913.

MLA Handbook (7th Edition):

Santos, Shana Marie. “Understanding the Enzyme-inhibitor Interaction within the Substrate Pocket of Protein Tyrosine Kinases.” 2013. Web. 26 Jun 2019.

Vancouver:

Santos SM. Understanding the Enzyme-inhibitor Interaction within the Substrate Pocket of Protein Tyrosine Kinases. [Internet] [Doctoral dissertation]. University of Michigan; 2013. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/99913.

Council of Science Editors:

Santos SM. Understanding the Enzyme-inhibitor Interaction within the Substrate Pocket of Protein Tyrosine Kinases. [Doctoral Dissertation]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/99913

20. Lofgren, Michael W. Auxiliary Proteins and Allosteric Control of the Mitochondrial Branch of B12 Trafficking, Assembly, and Reactivity.

Degree: PhD, Biological Chemistry, 2013, University of Michigan

 The presence of cofactors in enzymes broadens the range of chemical transformations catalyzed in Nature. Adenosylcobalamin (AdoCbl) or coenzyme-B12, is a biologically active derivative of… (more)

Subjects/Keywords: B12 Trafficking Proteins; Allostery; Biological Chemistry; Science

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APA (6th Edition):

Lofgren, M. W. (2013). Auxiliary Proteins and Allosteric Control of the Mitochondrial Branch of B12 Trafficking, Assembly, and Reactivity. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/99939

Chicago Manual of Style (16th Edition):

Lofgren, Michael W. “Auxiliary Proteins and Allosteric Control of the Mitochondrial Branch of B12 Trafficking, Assembly, and Reactivity.” 2013. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/99939.

MLA Handbook (7th Edition):

Lofgren, Michael W. “Auxiliary Proteins and Allosteric Control of the Mitochondrial Branch of B12 Trafficking, Assembly, and Reactivity.” 2013. Web. 26 Jun 2019.

Vancouver:

Lofgren MW. Auxiliary Proteins and Allosteric Control of the Mitochondrial Branch of B12 Trafficking, Assembly, and Reactivity. [Internet] [Doctoral dissertation]. University of Michigan; 2013. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/99939.

Council of Science Editors:

Lofgren MW. Auxiliary Proteins and Allosteric Control of the Mitochondrial Branch of B12 Trafficking, Assembly, and Reactivity. [Doctoral Dissertation]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/99939

21. Roman Melendez, Gabriel David. Studies on the Radical Enzymes Glutamate Mutase and Viperin.

Degree: PhD, Chemistry, 2015, University of Michigan

 Adenosylcobalamin (coenzyme B12) serves as a source of organic radicals that are generated by homolytic scission of the cobalt-carbon bond to form cob(II)alamin and a… (more)

Subjects/Keywords: Adenosylcobalamin (Coenzyme B12) Enzymes; Glutamate Mutase; Magnetic Field Effect Studies on Glutamate Mutase; Radical S-Adenosyl-L-Methionine (SAM) Enzymes; Viperin; Farnesyl Pyrophosphate Synthase; Chemistry; Science

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APA (6th Edition):

Roman Melendez, G. D. (2015). Studies on the Radical Enzymes Glutamate Mutase and Viperin. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/111388

Chicago Manual of Style (16th Edition):

Roman Melendez, Gabriel David. “Studies on the Radical Enzymes Glutamate Mutase and Viperin.” 2015. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/111388.

MLA Handbook (7th Edition):

Roman Melendez, Gabriel David. “Studies on the Radical Enzymes Glutamate Mutase and Viperin.” 2015. Web. 26 Jun 2019.

Vancouver:

Roman Melendez GD. Studies on the Radical Enzymes Glutamate Mutase and Viperin. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/111388.

Council of Science Editors:

Roman Melendez GD. Studies on the Radical Enzymes Glutamate Mutase and Viperin. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/111388

22. Yoon, Miri. Mechanistic Studies on AdoCbl-dependent Glutamate Mutase.

Degree: PhD, Chemistry, 2009, University of Michigan

 Adenosylcobalamin (AdoCbl) serves as a source of free radicals for a group of enzymes that catalyze unusual rearrangements involving hydrogen atom migration and proceed through… (more)

Subjects/Keywords: Coenzyme B12; Glutamate Mutase; Kinetic Isotope Effect; Hydrogen Tunneling; Radical Enzyme; Chemistry; Science

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APA (6th Edition):

Yoon, M. (2009). Mechanistic Studies on AdoCbl-dependent Glutamate Mutase. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/63638

Chicago Manual of Style (16th Edition):

Yoon, Miri. “Mechanistic Studies on AdoCbl-dependent Glutamate Mutase.” 2009. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/63638.

MLA Handbook (7th Edition):

Yoon, Miri. “Mechanistic Studies on AdoCbl-dependent Glutamate Mutase.” 2009. Web. 26 Jun 2019.

Vancouver:

Yoon M. Mechanistic Studies on AdoCbl-dependent Glutamate Mutase. [Internet] [Doctoral dissertation]. University of Michigan; 2009. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/63638.

Council of Science Editors:

Yoon M. Mechanistic Studies on AdoCbl-dependent Glutamate Mutase. [Doctoral Dissertation]. University of Michigan; 2009. Available from: http://hdl.handle.net/2027.42/63638

23. Nanga, Ravi Prakash Reddy. Structural Investigation of Helical Intermediates in the Misfolding Pathway of Amyloid Peptides Associated With Type II Diabetes and HIV.

Degree: PhD, Chemistry, 2011, University of Michigan

 A variety of aging related diseases including Alzheimer’s, Type II diabetes, Huntington’s, Parkinson’s, and Creutzfeldt-Jakob are characterized by the formation of abnormal proteinaceous deposits. These… (more)

Subjects/Keywords: Alpha-helical Intermediate Structures of IAPP and PAP248-286 in Micelles by Solution NMR Spectroscopy; Islet Amyloid Poly Peptide (IAPP); Amylin; Prostatic Acid Phosphatase Fragment 248-286; Semen-derived Enhancer of Viral Infection (SEVI); Chemistry; Science

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APA (6th Edition):

Nanga, R. P. R. (2011). Structural Investigation of Helical Intermediates in the Misfolding Pathway of Amyloid Peptides Associated With Type II Diabetes and HIV. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/86258

Chicago Manual of Style (16th Edition):

Nanga, Ravi Prakash Reddy. “Structural Investigation of Helical Intermediates in the Misfolding Pathway of Amyloid Peptides Associated With Type II Diabetes and HIV.” 2011. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/86258.

MLA Handbook (7th Edition):

Nanga, Ravi Prakash Reddy. “Structural Investigation of Helical Intermediates in the Misfolding Pathway of Amyloid Peptides Associated With Type II Diabetes and HIV.” 2011. Web. 26 Jun 2019.

Vancouver:

Nanga RPR. Structural Investigation of Helical Intermediates in the Misfolding Pathway of Amyloid Peptides Associated With Type II Diabetes and HIV. [Internet] [Doctoral dissertation]. University of Michigan; 2011. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/86258.

Council of Science Editors:

Nanga RPR. Structural Investigation of Helical Intermediates in the Misfolding Pathway of Amyloid Peptides Associated With Type II Diabetes and HIV. [Doctoral Dissertation]. University of Michigan; 2011. Available from: http://hdl.handle.net/2027.42/86258

24. Smith, Richard D. Biophysical Properties of Small Molecules Binding to Proteins.

Degree: PhD, Biophysics, 2010, University of Michigan

 Binding MOAD (Mother of All Databases) is the largest collection of high-quality, protein–ligand complexes. Binding MOAD contains 13138 protein–ligand complexes comprised of 4078 unique protein… (more)

Subjects/Keywords: Protein-Ligand Binding; Protein-Small Molecule Binding; Biological Chemistry; Science

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APA (6th Edition):

Smith, R. D. (2010). Biophysical Properties of Small Molecules Binding to Proteins. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/75969

Chicago Manual of Style (16th Edition):

Smith, Richard D. “Biophysical Properties of Small Molecules Binding to Proteins.” 2010. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/75969.

MLA Handbook (7th Edition):

Smith, Richard D. “Biophysical Properties of Small Molecules Binding to Proteins.” 2010. Web. 26 Jun 2019.

Vancouver:

Smith RD. Biophysical Properties of Small Molecules Binding to Proteins. [Internet] [Doctoral dissertation]. University of Michigan; 2010. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/75969.

Council of Science Editors:

Smith RD. Biophysical Properties of Small Molecules Binding to Proteins. [Doctoral Dissertation]. University of Michigan; 2010. Available from: http://hdl.handle.net/2027.42/75969

25. Buer, Benjamin Curtis. Structural and Thermodynamic Investigation Into the Effects of Protein Fluorination.

Degree: PhD, Chemical Biology, 2012, University of Michigan

 The introduction of non-canonical amino acids has been a useful tool to modify the properties of proteins. In particular, highly fluorinated amino acids have shown… (more)

Subjects/Keywords: Fluorous Proteins; Chemistry; Science

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APA (6th Edition):

Buer, B. C. (2012). Structural and Thermodynamic Investigation Into the Effects of Protein Fluorination. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/94053

Chicago Manual of Style (16th Edition):

Buer, Benjamin Curtis. “Structural and Thermodynamic Investigation Into the Effects of Protein Fluorination.” 2012. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/94053.

MLA Handbook (7th Edition):

Buer, Benjamin Curtis. “Structural and Thermodynamic Investigation Into the Effects of Protein Fluorination.” 2012. Web. 26 Jun 2019.

Vancouver:

Buer BC. Structural and Thermodynamic Investigation Into the Effects of Protein Fluorination. [Internet] [Doctoral dissertation]. University of Michigan; 2012. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/94053.

Council of Science Editors:

Buer BC. Structural and Thermodynamic Investigation Into the Effects of Protein Fluorination. [Doctoral Dissertation]. University of Michigan; 2012. Available from: http://hdl.handle.net/2027.42/94053


University of Michigan

26. Li, Jingjing. Substrate Specificity and Metal Requirements of 3-Deoxy-D-manno-octulosonate 8-Phosphate Synthase (KDOPS).

Degree: PhD, Chemistry, 2008, University of Michigan

 3-Deoxy-D-manno-octulosonate 8-phosphate synthase (KDOPS) catalyzes the aldol-type condensation of D-arabinose 5-phosphate (A5P) and phosphoenolpyruvate (PEP) to form 3-deoxy-D-manno-octulosonate 8-phosphate (KDO8P) and inorganic phosphate. This reaction… (more)

Subjects/Keywords: KDOPS; Substrate Specificity; Metal Requirements; Chemistry; Science

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APA (6th Edition):

Li, J. (2008). Substrate Specificity and Metal Requirements of 3-Deoxy-D-manno-octulosonate 8-Phosphate Synthase (KDOPS). (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/58440

Chicago Manual of Style (16th Edition):

Li, Jingjing. “Substrate Specificity and Metal Requirements of 3-Deoxy-D-manno-octulosonate 8-Phosphate Synthase (KDOPS).” 2008. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/58440.

MLA Handbook (7th Edition):

Li, Jingjing. “Substrate Specificity and Metal Requirements of 3-Deoxy-D-manno-octulosonate 8-Phosphate Synthase (KDOPS).” 2008. Web. 26 Jun 2019.

Vancouver:

Li J. Substrate Specificity and Metal Requirements of 3-Deoxy-D-manno-octulosonate 8-Phosphate Synthase (KDOPS). [Internet] [Doctoral dissertation]. University of Michigan; 2008. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/58440.

Council of Science Editors:

Li J. Substrate Specificity and Metal Requirements of 3-Deoxy-D-manno-octulosonate 8-Phosphate Synthase (KDOPS). [Doctoral Dissertation]. University of Michigan; 2008. Available from: http://hdl.handle.net/2027.42/58440


University of Michigan

27. Lee, Hyang-Yeol. Design of New Bio-Materials: Fluorous Peptides and Metal-Peptides Frameworks.

Degree: PhD, Chemistry, 2008, University of Michigan

 Perfluorocarbons have unique and valuable physical properties not found in Nature. By incorporating fluorine into proteins, it might be possible to produce biological molecules with… (more)

Subjects/Keywords: Fluorinated Protein; Metal-Peptides Frameworks; Chemistry; Science

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APA (6th Edition):

Lee, H. (2008). Design of New Bio-Materials: Fluorous Peptides and Metal-Peptides Frameworks. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/58424

Chicago Manual of Style (16th Edition):

Lee, Hyang-Yeol. “Design of New Bio-Materials: Fluorous Peptides and Metal-Peptides Frameworks.” 2008. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/58424.

MLA Handbook (7th Edition):

Lee, Hyang-Yeol. “Design of New Bio-Materials: Fluorous Peptides and Metal-Peptides Frameworks.” 2008. Web. 26 Jun 2019.

Vancouver:

Lee H. Design of New Bio-Materials: Fluorous Peptides and Metal-Peptides Frameworks. [Internet] [Doctoral dissertation]. University of Michigan; 2008. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/58424.

Council of Science Editors:

Lee H. Design of New Bio-Materials: Fluorous Peptides and Metal-Peptides Frameworks. [Doctoral Dissertation]. University of Michigan; 2008. Available from: http://hdl.handle.net/2027.42/58424


University of Michigan

28. Gottler, Lindsey Marie. Peptides as Models Systems, Antimicrobial Agents, and a Means for Protein Superassembly.

Degree: PhD, Chemistry, 2008, University of Michigan

 Proteins are the most diverse class of biomolecules, both structurally and functionally, and have evolved to accomplish many tasks in living systems. The features of… (more)

Subjects/Keywords: Antimicrobial Peptides; De Novo Designed Coiled Coils; Fluorous Amino Acids; Protein Self-assembly; Biological Chemistry; Chemistry; Science

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APA (6th Edition):

Gottler, L. M. (2008). Peptides as Models Systems, Antimicrobial Agents, and a Means for Protein Superassembly. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/60840

Chicago Manual of Style (16th Edition):

Gottler, Lindsey Marie. “Peptides as Models Systems, Antimicrobial Agents, and a Means for Protein Superassembly.” 2008. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/60840.

MLA Handbook (7th Edition):

Gottler, Lindsey Marie. “Peptides as Models Systems, Antimicrobial Agents, and a Means for Protein Superassembly.” 2008. Web. 26 Jun 2019.

Vancouver:

Gottler LM. Peptides as Models Systems, Antimicrobial Agents, and a Means for Protein Superassembly. [Internet] [Doctoral dissertation]. University of Michigan; 2008. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/60840.

Council of Science Editors:

Gottler LM. Peptides as Models Systems, Antimicrobial Agents, and a Means for Protein Superassembly. [Doctoral Dissertation]. University of Michigan; 2008. Available from: http://hdl.handle.net/2027.42/60840


University of Michigan

29. Kalli, Anastasia. Protein and Lantibiotic Sequencing by Gas Phase Dissociation Involving Vibrational Excitation and Ion Electron Reactions.

Degree: PhD, Chemistry, 2009, University of Michigan

 In proteomics, protein identification and characterization are largely performed by tandem mass spectrometry (MS/MS), in which sequence specific product ions are generated from precursor peptide… (more)

Subjects/Keywords: Fourier Transform Ion Cyclotron Mass Spectrmetry; Ion-Electron Reactions; Peptide Sequencing; Lantibiotics; Chemistry; Science

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APA (6th Edition):

Kalli, A. (2009). Protein and Lantibiotic Sequencing by Gas Phase Dissociation Involving Vibrational Excitation and Ion Electron Reactions. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/62221

Chicago Manual of Style (16th Edition):

Kalli, Anastasia. “Protein and Lantibiotic Sequencing by Gas Phase Dissociation Involving Vibrational Excitation and Ion Electron Reactions.” 2009. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/62221.

MLA Handbook (7th Edition):

Kalli, Anastasia. “Protein and Lantibiotic Sequencing by Gas Phase Dissociation Involving Vibrational Excitation and Ion Electron Reactions.” 2009. Web. 26 Jun 2019.

Vancouver:

Kalli A. Protein and Lantibiotic Sequencing by Gas Phase Dissociation Involving Vibrational Excitation and Ion Electron Reactions. [Internet] [Doctoral dissertation]. University of Michigan; 2009. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/62221.

Council of Science Editors:

Kalli A. Protein and Lantibiotic Sequencing by Gas Phase Dissociation Involving Vibrational Excitation and Ion Electron Reactions. [Doctoral Dissertation]. University of Michigan; 2009. Available from: http://hdl.handle.net/2027.42/62221


University of Michigan

30. Sundberg, Thomas B. Elucidation of Anti-Proliferative and Pro-Apoptotic Signaling Induced by the Immunomodulatory Benzodiazepine Bz-423.

Degree: PhD, Chemistry, 2009, University of Michigan

 Bz-423 is a non-anxiolytic 1,4-benzodiazepine that ameliorates disease in animal models of lupus, arthritis and psoriasis. Concomitant with these therapeutic effects, Bz-423 induces lineage-specific apoptosis… (more)

Subjects/Keywords: Mitochondrial FoF1-ATPase; Lupus; T Cell Apoptosis; Myc; Reactive Oxygen Species Signaling; Noxa; Biological Chemistry; Science

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APA (6th Edition):

Sundberg, T. B. (2009). Elucidation of Anti-Proliferative and Pro-Apoptotic Signaling Induced by the Immunomodulatory Benzodiazepine Bz-423. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/62392

Chicago Manual of Style (16th Edition):

Sundberg, Thomas B. “Elucidation of Anti-Proliferative and Pro-Apoptotic Signaling Induced by the Immunomodulatory Benzodiazepine Bz-423.” 2009. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/62392.

MLA Handbook (7th Edition):

Sundberg, Thomas B. “Elucidation of Anti-Proliferative and Pro-Apoptotic Signaling Induced by the Immunomodulatory Benzodiazepine Bz-423.” 2009. Web. 26 Jun 2019.

Vancouver:

Sundberg TB. Elucidation of Anti-Proliferative and Pro-Apoptotic Signaling Induced by the Immunomodulatory Benzodiazepine Bz-423. [Internet] [Doctoral dissertation]. University of Michigan; 2009. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/62392.

Council of Science Editors:

Sundberg TB. Elucidation of Anti-Proliferative and Pro-Apoptotic Signaling Induced by the Immunomodulatory Benzodiazepine Bz-423. [Doctoral Dissertation]. University of Michigan; 2009. Available from: http://hdl.handle.net/2027.42/62392

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