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You searched for subject:(Protein chemistry). Showing records 1 – 30 of 1094 total matches.

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1. Kapella, Anna. Σχεδιασμός και σύνθεση οργανικών ενώσεων με εφαρμογές στη φαρμακοχημεία και σε τεχνολογία ηλεκτρονικών διατάξεων.

Degree: 2018, Agricultural University of Athens; Γεωπονικό Πανεπιστήμιο Αθηνών

 The present thesis consists of two major thematic units.In the first part of the present thesis, the design and synthesis of PI3Kα inhibitors is described.… (more)

Subjects/Keywords: Οργανική σύνθεση; Ορθολογικός σχεδιασμός φαρμάκων; Ένωση - οδηγός; Βελτιστοποίηση; Αναστολή πρωτεϊνών; Ηλεκτρονική διάταξη; Ανθρακένιο; Φωτοευαίσθητα υλικά; Κατεργασία σε διάλυμα; Κετάλη; Σχηματισμός υμενίων; Φαρμακοχημεία; Μικροηλεκτρονική; Organic synthesis; Rational drug design; lead compound; Optimization; Protein inhibition; Electronic device; Anthracene; Photosensitive compounds; Solution processing; Ketal; Film formation; Pharmaceutical chemistry; Microelectronics

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APA (6th Edition):

Kapella, A. (2018). Σχεδιασμός και σύνθεση οργανικών ενώσεων με εφαρμογές στη φαρμακοχημεία και σε τεχνολογία ηλεκτρονικών διατάξεων. (Thesis). Agricultural University of Athens; Γεωπονικό Πανεπιστήμιο Αθηνών. Retrieved from http://hdl.handle.net/10442/hedi/45127

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

Chicago Manual of Style (16th Edition):

Kapella, Anna. “Σχεδιασμός και σύνθεση οργανικών ενώσεων με εφαρμογές στη φαρμακοχημεία και σε τεχνολογία ηλεκτρονικών διατάξεων.” 2018. Thesis, Agricultural University of Athens; Γεωπονικό Πανεπιστήμιο Αθηνών. Accessed June 19, 2019. http://hdl.handle.net/10442/hedi/45127.

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

MLA Handbook (7th Edition):

Kapella, Anna. “Σχεδιασμός και σύνθεση οργανικών ενώσεων με εφαρμογές στη φαρμακοχημεία και σε τεχνολογία ηλεκτρονικών διατάξεων.” 2018. Web. 19 Jun 2019.

Vancouver:

Kapella A. Σχεδιασμός και σύνθεση οργανικών ενώσεων με εφαρμογές στη φαρμακοχημεία και σε τεχνολογία ηλεκτρονικών διατάξεων. [Internet] [Thesis]. Agricultural University of Athens; Γεωπονικό Πανεπιστήμιο Αθηνών; 2018. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/10442/hedi/45127.

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

Council of Science Editors:

Kapella A. Σχεδιασμός και σύνθεση οργανικών ενώσεων με εφαρμογές στη φαρμακοχημεία και σε τεχνολογία ηλεκτρονικών διατάξεων. [Thesis]. Agricultural University of Athens; Γεωπονικό Πανεπιστήμιο Αθηνών; 2018. Available from: http://hdl.handle.net/10442/hedi/45127

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


Arizona State University

2. Sommer, Dayn Joseph. Design of Protein-Based Hybrid Catalysts for Fuel Production.

Degree: Biochemistry, 2016, Arizona State University

Subjects/Keywords: Biochemistry; Inorganic chemistry; Cobalt catalysts; Computational chemistry; Fuel production; Iron-sulfur clusters; Protein engineering; Redox chemistry

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APA (6th Edition):

Sommer, D. J. (2016). Design of Protein-Based Hybrid Catalysts for Fuel Production. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/38409

Chicago Manual of Style (16th Edition):

Sommer, Dayn Joseph. “Design of Protein-Based Hybrid Catalysts for Fuel Production.” 2016. Doctoral Dissertation, Arizona State University. Accessed June 19, 2019. http://repository.asu.edu/items/38409.

MLA Handbook (7th Edition):

Sommer, Dayn Joseph. “Design of Protein-Based Hybrid Catalysts for Fuel Production.” 2016. Web. 19 Jun 2019.

Vancouver:

Sommer DJ. Design of Protein-Based Hybrid Catalysts for Fuel Production. [Internet] [Doctoral dissertation]. Arizona State University; 2016. [cited 2019 Jun 19]. Available from: http://repository.asu.edu/items/38409.

Council of Science Editors:

Sommer DJ. Design of Protein-Based Hybrid Catalysts for Fuel Production. [Doctoral Dissertation]. Arizona State University; 2016. Available from: http://repository.asu.edu/items/38409


Arizona State University

3. Maini, Rumit. Study of Ribosomes having Modifications in the Peptidyltransferase Center Using Non-α-L-Amino Acids and Synthesis and Biological Evaluation of Topopyrones.

Degree: PhD, Chemistry, 2013, Arizona State University

 The ribosome is a ribozyme and central to the biosynthesis of proteins in all organisms. It has a strong bias against non-alpha-L-amino acids, such as… (more)

Subjects/Keywords: Chemistry; Biochemistry; in vitro protein expression; modified ribosomes; peptidomimetics; ribosomes; topopyrones

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APA (6th Edition):

Maini, R. (2013). Study of Ribosomes having Modifications in the Peptidyltransferase Center Using Non-α-L-Amino Acids and Synthesis and Biological Evaluation of Topopyrones. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/18753

Chicago Manual of Style (16th Edition):

Maini, Rumit. “Study of Ribosomes having Modifications in the Peptidyltransferase Center Using Non-α-L-Amino Acids and Synthesis and Biological Evaluation of Topopyrones.” 2013. Doctoral Dissertation, Arizona State University. Accessed June 19, 2019. http://repository.asu.edu/items/18753.

MLA Handbook (7th Edition):

Maini, Rumit. “Study of Ribosomes having Modifications in the Peptidyltransferase Center Using Non-α-L-Amino Acids and Synthesis and Biological Evaluation of Topopyrones.” 2013. Web. 19 Jun 2019.

Vancouver:

Maini R. Study of Ribosomes having Modifications in the Peptidyltransferase Center Using Non-α-L-Amino Acids and Synthesis and Biological Evaluation of Topopyrones. [Internet] [Doctoral dissertation]. Arizona State University; 2013. [cited 2019 Jun 19]. Available from: http://repository.asu.edu/items/18753.

Council of Science Editors:

Maini R. Study of Ribosomes having Modifications in the Peptidyltransferase Center Using Non-α-L-Amino Acids and Synthesis and Biological Evaluation of Topopyrones. [Doctoral Dissertation]. Arizona State University; 2013. Available from: http://repository.asu.edu/items/18753


Arizona State University

4. Roy Chowdhury, Sandipan. Synthesis of Methylene Blue Analogues as Multifunctional Radical Quenchers, Synthesis of Unnatural Amino Acids and Their Ribosomal Incorporation into Proteins.

Degree: Chemistry, 2016, Arizona State University

Subjects/Keywords: Chemistry; Biochemistry; Medicine; Antioxidant; Beta amino acid; Green fluorescent protein; In vitro protein synthesis; Methylene blue; Methylene violet

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APA (6th Edition):

Roy Chowdhury, S. (2016). Synthesis of Methylene Blue Analogues as Multifunctional Radical Quenchers, Synthesis of Unnatural Amino Acids and Their Ribosomal Incorporation into Proteins. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/37047

Chicago Manual of Style (16th Edition):

Roy Chowdhury, Sandipan. “Synthesis of Methylene Blue Analogues as Multifunctional Radical Quenchers, Synthesis of Unnatural Amino Acids and Their Ribosomal Incorporation into Proteins.” 2016. Doctoral Dissertation, Arizona State University. Accessed June 19, 2019. http://repository.asu.edu/items/37047.

MLA Handbook (7th Edition):

Roy Chowdhury, Sandipan. “Synthesis of Methylene Blue Analogues as Multifunctional Radical Quenchers, Synthesis of Unnatural Amino Acids and Their Ribosomal Incorporation into Proteins.” 2016. Web. 19 Jun 2019.

Vancouver:

Roy Chowdhury S. Synthesis of Methylene Blue Analogues as Multifunctional Radical Quenchers, Synthesis of Unnatural Amino Acids and Their Ribosomal Incorporation into Proteins. [Internet] [Doctoral dissertation]. Arizona State University; 2016. [cited 2019 Jun 19]. Available from: http://repository.asu.edu/items/37047.

Council of Science Editors:

Roy Chowdhury S. Synthesis of Methylene Blue Analogues as Multifunctional Radical Quenchers, Synthesis of Unnatural Amino Acids and Their Ribosomal Incorporation into Proteins. [Doctoral Dissertation]. Arizona State University; 2016. Available from: http://repository.asu.edu/items/37047

5. Addison, John Bennett. Determining the Molecular Structure of Animal Silks and Related Peptide Mimics.

Degree: Biochemistry, 2014, Arizona State University

Subjects/Keywords: Biochemistry; Polymer chemistry; Molecular biology; caddisfly; NMR; protein; silk; structure; webspinner

…Representations of the Primary Protein Sequences of Various SilkProducing Arthropods… …Partial Amino Acid Sequences of Heavy-chain Fibroin Protein from the Caddisfly Species… …52 3.1 Extended D-Repeat from the H-Fibroin Protein Sequence from the Species… …insoluble protein-based biopolymer fibers spun by arthropods, that prior to spinning are soluble… …repetitive protein aggregates composed primarily of nonessential amino acids glycine, alanine, and… 

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APA (6th Edition):

Addison, J. B. (2014). Determining the Molecular Structure of Animal Silks and Related Peptide Mimics. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/25937

Chicago Manual of Style (16th Edition):

Addison, John Bennett. “Determining the Molecular Structure of Animal Silks and Related Peptide Mimics.” 2014. Doctoral Dissertation, Arizona State University. Accessed June 19, 2019. http://repository.asu.edu/items/25937.

MLA Handbook (7th Edition):

Addison, John Bennett. “Determining the Molecular Structure of Animal Silks and Related Peptide Mimics.” 2014. Web. 19 Jun 2019.

Vancouver:

Addison JB. Determining the Molecular Structure of Animal Silks and Related Peptide Mimics. [Internet] [Doctoral dissertation]. Arizona State University; 2014. [cited 2019 Jun 19]. Available from: http://repository.asu.edu/items/25937.

Council of Science Editors:

Addison JB. Determining the Molecular Structure of Animal Silks and Related Peptide Mimics. [Doctoral Dissertation]. Arizona State University; 2014. Available from: http://repository.asu.edu/items/25937


Arizona State University

6. Spiriti, Justin Matthew. Applications of Adaptive Umbrella Sampling in Biomolecular Simulation.

Degree: PhD, Chemistry, 2011, Arizona State University

 Conformational changes in biomolecules often take place on longer timescales than are easily accessible with unbiased molecular dynamics simulations, necessitating the use of enhanced sampling… (more)

Subjects/Keywords: Biophysics; Biochemistry; Physical Chemistry; adaptive umbrella sampling; cis peptide bond; Cy3-DNA interaction; DNA flexibility; molecular dynamics simulation; protein glycosylation

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APA (6th Edition):

Spiriti, J. M. (2011). Applications of Adaptive Umbrella Sampling in Biomolecular Simulation. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/9414

Chicago Manual of Style (16th Edition):

Spiriti, Justin Matthew. “Applications of Adaptive Umbrella Sampling in Biomolecular Simulation.” 2011. Doctoral Dissertation, Arizona State University. Accessed June 19, 2019. http://repository.asu.edu/items/9414.

MLA Handbook (7th Edition):

Spiriti, Justin Matthew. “Applications of Adaptive Umbrella Sampling in Biomolecular Simulation.” 2011. Web. 19 Jun 2019.

Vancouver:

Spiriti JM. Applications of Adaptive Umbrella Sampling in Biomolecular Simulation. [Internet] [Doctoral dissertation]. Arizona State University; 2011. [cited 2019 Jun 19]. Available from: http://repository.asu.edu/items/9414.

Council of Science Editors:

Spiriti JM. Applications of Adaptive Umbrella Sampling in Biomolecular Simulation. [Doctoral Dissertation]. Arizona State University; 2011. Available from: http://repository.asu.edu/items/9414


Arizona State University

7. Yan, Qin. Characterization of Small Metal-binding Protein (SmbP) From Nitrosomonas Europaea.

Degree: PhD, Chemistry, 2010, Arizona State University

 A novel small metal-binding protein (SmbP), with only 93 residues and no similarity to other known proteins, has been isolated from the periplasm of Nitrosomonas… (more)

Subjects/Keywords: Chemistry; Biochemistry; Copper Binding; Nitrosomonas Europaea; Small Metal-binding Protein

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APA (6th Edition):

Yan, Q. (2010). Characterization of Small Metal-binding Protein (SmbP) From Nitrosomonas Europaea. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/8666

Chicago Manual of Style (16th Edition):

Yan, Qin. “Characterization of Small Metal-binding Protein (SmbP) From Nitrosomonas Europaea.” 2010. Doctoral Dissertation, Arizona State University. Accessed June 19, 2019. http://repository.asu.edu/items/8666.

MLA Handbook (7th Edition):

Yan, Qin. “Characterization of Small Metal-binding Protein (SmbP) From Nitrosomonas Europaea.” 2010. Web. 19 Jun 2019.

Vancouver:

Yan Q. Characterization of Small Metal-binding Protein (SmbP) From Nitrosomonas Europaea. [Internet] [Doctoral dissertation]. Arizona State University; 2010. [cited 2019 Jun 19]. Available from: http://repository.asu.edu/items/8666.

Council of Science Editors:

Yan Q. Characterization of Small Metal-binding Protein (SmbP) From Nitrosomonas Europaea. [Doctoral Dissertation]. Arizona State University; 2010. Available from: http://repository.asu.edu/items/8666

8. Kim, Hanseong. Color Evolution of Kaede-type Red Fluorescent Proteins.

Degree: PhD, Chemistry, 2012, Arizona State University

 The green fluorescent protein (GFP)-like fluorescent proteins play an important role for the color of reef-building corals. Different colors of extant coral fluorescent proteins (FPs)… (more)

Subjects/Keywords: Biochemistry; Chemistry; Fluorescent Protein; GFP; Kaede; Photoconversion

…Photoconversion Protein .. …...12 3. Proposed Mechanism of the Green-to-Red Photoconversion Reaction… …95 ix INTRODUCTION Most naturally occurring green fluorescent protein (GFP)… …helical conformation in the interior of the native protein (3). When this tripeptide… …desaturation within the chromophore coupled with the chemical environment of the surrounding protein… …matrix dictates the wavelength of light emitted by the protein. Manipulation of these… 

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APA (6th Edition):

Kim, H. (2012). Color Evolution of Kaede-type Red Fluorescent Proteins. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/14732

Chicago Manual of Style (16th Edition):

Kim, Hanseong. “Color Evolution of Kaede-type Red Fluorescent Proteins.” 2012. Doctoral Dissertation, Arizona State University. Accessed June 19, 2019. http://repository.asu.edu/items/14732.

MLA Handbook (7th Edition):

Kim, Hanseong. “Color Evolution of Kaede-type Red Fluorescent Proteins.” 2012. Web. 19 Jun 2019.

Vancouver:

Kim H. Color Evolution of Kaede-type Red Fluorescent Proteins. [Internet] [Doctoral dissertation]. Arizona State University; 2012. [cited 2019 Jun 19]. Available from: http://repository.asu.edu/items/14732.

Council of Science Editors:

Kim H. Color Evolution of Kaede-type Red Fluorescent Proteins. [Doctoral Dissertation]. Arizona State University; 2012. Available from: http://repository.asu.edu/items/14732


Arizona State University

9. Morgan, Ashli. Identification of Structural Mechanisms that Modulate Glycosaminoglycan Affinity in Various Strains of Decorin Binding Protein A.

Degree: Biochemistry, 2015, Arizona State University

 Glycosaminoglycans (GAGs) are a class of complex biomolecules comprised of linear, sulfated polysaccharides whose presence on cell surfaces and in the extracellular matrix involve them… (more)

Subjects/Keywords: Biochemistry; Biophysics; Chemistry; Decorin Binding Protein; Glycosaminoglycan; Glycosaminoglycan-binding protein; Lyme disease; NMR (nuclear magnetic resonance)

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APA (6th Edition):

Morgan, A. (2015). Identification of Structural Mechanisms that Modulate Glycosaminoglycan Affinity in Various Strains of Decorin Binding Protein A. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/34887

Chicago Manual of Style (16th Edition):

Morgan, Ashli. “Identification of Structural Mechanisms that Modulate Glycosaminoglycan Affinity in Various Strains of Decorin Binding Protein A.” 2015. Doctoral Dissertation, Arizona State University. Accessed June 19, 2019. http://repository.asu.edu/items/34887.

MLA Handbook (7th Edition):

Morgan, Ashli. “Identification of Structural Mechanisms that Modulate Glycosaminoglycan Affinity in Various Strains of Decorin Binding Protein A.” 2015. Web. 19 Jun 2019.

Vancouver:

Morgan A. Identification of Structural Mechanisms that Modulate Glycosaminoglycan Affinity in Various Strains of Decorin Binding Protein A. [Internet] [Doctoral dissertation]. Arizona State University; 2015. [cited 2019 Jun 19]. Available from: http://repository.asu.edu/items/34887.

Council of Science Editors:

Morgan A. Identification of Structural Mechanisms that Modulate Glycosaminoglycan Affinity in Various Strains of Decorin Binding Protein A. [Doctoral Dissertation]. Arizona State University; 2015. Available from: http://repository.asu.edu/items/34887


Arizona State University

10. Chakraborty, Manas. Investigating the Stoichiometry of RuBisCO Activase by Fluorescence Fluctuation Spectroscopy.

Degree: PhD, Chemistry, 2014, Arizona State University

 Ribulose-1, 5-bisphosphate carboxylase oxygenase, commonly known as RuBisCO, is an enzyme involved in carbon fixation in photosynthetic organisms. The enzyme is subject to a mechanism-based… (more)

Subjects/Keywords: Chemistry; Biophysics; FCS; PCH; Protein oligomerization; Rubisco Activase

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APA (6th Edition):

Chakraborty, M. (2014). Investigating the Stoichiometry of RuBisCO Activase by Fluorescence Fluctuation Spectroscopy. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/25170

Chicago Manual of Style (16th Edition):

Chakraborty, Manas. “Investigating the Stoichiometry of RuBisCO Activase by Fluorescence Fluctuation Spectroscopy.” 2014. Doctoral Dissertation, Arizona State University. Accessed June 19, 2019. http://repository.asu.edu/items/25170.

MLA Handbook (7th Edition):

Chakraborty, Manas. “Investigating the Stoichiometry of RuBisCO Activase by Fluorescence Fluctuation Spectroscopy.” 2014. Web. 19 Jun 2019.

Vancouver:

Chakraborty M. Investigating the Stoichiometry of RuBisCO Activase by Fluorescence Fluctuation Spectroscopy. [Internet] [Doctoral dissertation]. Arizona State University; 2014. [cited 2019 Jun 19]. Available from: http://repository.asu.edu/items/25170.

Council of Science Editors:

Chakraborty M. Investigating the Stoichiometry of RuBisCO Activase by Fluorescence Fluctuation Spectroscopy. [Doctoral Dissertation]. Arizona State University; 2014. Available from: http://repository.asu.edu/items/25170


Arizona State University

11. Petritis, Brianne Ogata. Large-Scale Kinetic Analyses of Protein-Protein Interactions: Advancing the Understanding of Post Translational Modifications in Biological Regulation.

Degree: Biological Design, 2018, Arizona State University

 Signal transduction networks comprising protein-protein interactions (PPIs) mediate homeostatic, diseased, and therapeutic cellular responses. Mapping these networks has primarily focused on identifying interactors, but less… (more)

Subjects/Keywords: Biochemistry; Molecular biology; Physical chemistry; kinetics; NAPPA; protein microarray; protein-protein interactions; SPRi; surface plasmon resonance

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APA (6th Edition):

Petritis, B. O. (2018). Large-Scale Kinetic Analyses of Protein-Protein Interactions: Advancing the Understanding of Post Translational Modifications in Biological Regulation. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/49378

Chicago Manual of Style (16th Edition):

Petritis, Brianne Ogata. “Large-Scale Kinetic Analyses of Protein-Protein Interactions: Advancing the Understanding of Post Translational Modifications in Biological Regulation.” 2018. Doctoral Dissertation, Arizona State University. Accessed June 19, 2019. http://repository.asu.edu/items/49378.

MLA Handbook (7th Edition):

Petritis, Brianne Ogata. “Large-Scale Kinetic Analyses of Protein-Protein Interactions: Advancing the Understanding of Post Translational Modifications in Biological Regulation.” 2018. Web. 19 Jun 2019.

Vancouver:

Petritis BO. Large-Scale Kinetic Analyses of Protein-Protein Interactions: Advancing the Understanding of Post Translational Modifications in Biological Regulation. [Internet] [Doctoral dissertation]. Arizona State University; 2018. [cited 2019 Jun 19]. Available from: http://repository.asu.edu/items/49378.

Council of Science Editors:

Petritis BO. Large-Scale Kinetic Analyses of Protein-Protein Interactions: Advancing the Understanding of Post Translational Modifications in Biological Regulation. [Doctoral Dissertation]. Arizona State University; 2018. Available from: http://repository.asu.edu/items/49378


Arizona State University

12. Abdallah, Bahige Gary. Microfluidic Tools for Protein Crystallography.

Degree: Chemistry, 2016, Arizona State University

 X-ray crystallography is the most widely used method to determine the structure of proteins, providing an understanding of their functions in all aspects of life… (more)

Subjects/Keywords: Chemistry; Engineering; Nanotechnology; Crystallization; Crystallography; Dielectrophoresis; Microfluidics; Protein; Separations

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APA (6th Edition):

Abdallah, B. G. (2016). Microfluidic Tools for Protein Crystallography. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/38507

Chicago Manual of Style (16th Edition):

Abdallah, Bahige Gary. “Microfluidic Tools for Protein Crystallography.” 2016. Doctoral Dissertation, Arizona State University. Accessed June 19, 2019. http://repository.asu.edu/items/38507.

MLA Handbook (7th Edition):

Abdallah, Bahige Gary. “Microfluidic Tools for Protein Crystallography.” 2016. Web. 19 Jun 2019.

Vancouver:

Abdallah BG. Microfluidic Tools for Protein Crystallography. [Internet] [Doctoral dissertation]. Arizona State University; 2016. [cited 2019 Jun 19]. Available from: http://repository.asu.edu/items/38507.

Council of Science Editors:

Abdallah BG. Microfluidic Tools for Protein Crystallography. [Doctoral Dissertation]. Arizona State University; 2016. Available from: http://repository.asu.edu/items/38507


Arizona State University

13. Staton, Sarah J. R. New Methods for Biological and Environmental Protein Fingerprinting: From Traditional Techniques to New Technology.

Degree: PhD, Chemistry, 2011, Arizona State University

 A new challenge on the horizon is to utilize the large amounts of protein found in the atmosphere to identify different organisms from which the… (more)

Subjects/Keywords: Chemistry; amyloid protein; bioaerosol; dielectrophoresis; nanoparticles; remote detection; separation

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APA (6th Edition):

Staton, S. J. R. (2011). New Methods for Biological and Environmental Protein Fingerprinting: From Traditional Techniques to New Technology. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/9222

Chicago Manual of Style (16th Edition):

Staton, Sarah J R. “New Methods for Biological and Environmental Protein Fingerprinting: From Traditional Techniques to New Technology.” 2011. Doctoral Dissertation, Arizona State University. Accessed June 19, 2019. http://repository.asu.edu/items/9222.

MLA Handbook (7th Edition):

Staton, Sarah J R. “New Methods for Biological and Environmental Protein Fingerprinting: From Traditional Techniques to New Technology.” 2011. Web. 19 Jun 2019.

Vancouver:

Staton SJR. New Methods for Biological and Environmental Protein Fingerprinting: From Traditional Techniques to New Technology. [Internet] [Doctoral dissertation]. Arizona State University; 2011. [cited 2019 Jun 19]. Available from: http://repository.asu.edu/items/9222.

Council of Science Editors:

Staton SJR. New Methods for Biological and Environmental Protein Fingerprinting: From Traditional Techniques to New Technology. [Doctoral Dissertation]. Arizona State University; 2011. Available from: http://repository.asu.edu/items/9222


Arizona State University

14. Nangreave, Ryan Christopher. Novel Strategies for Producing Proteins with Non-Proteinogenic Amino Acids.

Degree: PhD, Chemistry, 2013, Arizona State University

 The biological and chemical diversity of protein structure and function can be greatly expanded by position-specific incorporation of non-natural amino acids bearing a variety of… (more)

Subjects/Keywords: Chemistry; Biochemistry; Amino Acid; Aminoacylated; Non-proteinogenic; Protein; Suppressor tRNA

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APA (6th Edition):

Nangreave, R. C. (2013). Novel Strategies for Producing Proteins with Non-Proteinogenic Amino Acids. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/20875

Chicago Manual of Style (16th Edition):

Nangreave, Ryan Christopher. “Novel Strategies for Producing Proteins with Non-Proteinogenic Amino Acids.” 2013. Doctoral Dissertation, Arizona State University. Accessed June 19, 2019. http://repository.asu.edu/items/20875.

MLA Handbook (7th Edition):

Nangreave, Ryan Christopher. “Novel Strategies for Producing Proteins with Non-Proteinogenic Amino Acids.” 2013. Web. 19 Jun 2019.

Vancouver:

Nangreave RC. Novel Strategies for Producing Proteins with Non-Proteinogenic Amino Acids. [Internet] [Doctoral dissertation]. Arizona State University; 2013. [cited 2019 Jun 19]. Available from: http://repository.asu.edu/items/20875.

Council of Science Editors:

Nangreave RC. Novel Strategies for Producing Proteins with Non-Proteinogenic Amino Acids. [Doctoral Dissertation]. Arizona State University; 2013. Available from: http://repository.asu.edu/items/20875

15. Wang, Wei. Exploring the Nature of Protein-Peptide Interactions on Surfaces.

Degree: Biochemistry, 2014, Arizona State University

Protein-surface interactions, no matter structured or unstructured, are important in both biological and man-made systems. Unstructured interactions are more difficult to study with conventional techniques… (more)

Subjects/Keywords: Biochemistry; Bioinformatics; Molecular chemistry; Additive binding; Length Dependence; Non-specific interaction; Peptide-antibody interaction; Peptide microarray; Protein-surface interaction

…CHAPTER Page 2 SELECTIVE PROTEIN-SURFACE INTERACTIONS AT SURFACES… …Protein Interactions ... 5 2.1. Summary of Proteins Used in the Binding Assays… …37 2.2. Peptide-Protein Binding Dynamic Range for Each Protein Sample ....... 41 S2.1… …Average Binding Affinity versus Length for Each Protein Sample ......... 47 2.4. β… …S2.2. Protein Mixture Binidng Distribution as a Function of Peptide Length . 59 x Figure… 

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

APA (6th Edition):

Wang, W. (2014). Exploring the Nature of Protein-Peptide Interactions on Surfaces. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/25814

Chicago Manual of Style (16th Edition):

Wang, Wei. “Exploring the Nature of Protein-Peptide Interactions on Surfaces.” 2014. Doctoral Dissertation, Arizona State University. Accessed June 19, 2019. http://repository.asu.edu/items/25814.

MLA Handbook (7th Edition):

Wang, Wei. “Exploring the Nature of Protein-Peptide Interactions on Surfaces.” 2014. Web. 19 Jun 2019.

Vancouver:

Wang W. Exploring the Nature of Protein-Peptide Interactions on Surfaces. [Internet] [Doctoral dissertation]. Arizona State University; 2014. [cited 2019 Jun 19]. Available from: http://repository.asu.edu/items/25814.

Council of Science Editors:

Wang W. Exploring the Nature of Protein-Peptide Interactions on Surfaces. [Doctoral Dissertation]. Arizona State University; 2014. Available from: http://repository.asu.edu/items/25814

16. Mcintosh, Chelsea Lee. The Investigation and Characterization of the Group 3 [NiFe]-Hydrogenases Using Protein Film Electrochemistry.

Degree: PhD, Biochemistry, 2012, Arizona State University

 Hydrogenases, the enzymes that reversibly convert protons and electrons to hydrogen, are used in all three domains of life. [NiFe]-hydrogenases are considered best suited for… (more)

Subjects/Keywords: Biochemistry; Energy; Chemistry; hydrogenase; protein electrochemistry; soluble

…150 
 
 
 x Chapter 1 Introduction: A Primer on Hydrogenases, Protein Film… …Jones§∞ § Department of Chemistry and Biochemistry and ∞Center for Bio-Inspired Solar Fuel… …basic enzymology of hydrogenases, the principles behind the technique protein film 2… …x5B;FeS] clusters linking the buried active site to the protein surface to allow fast… …proteins consist of a single monomeric protein housing only the H-cluster.40,41 Bacterial [… 

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APA (6th Edition):

Mcintosh, C. L. (2012). The Investigation and Characterization of the Group 3 [NiFe]-Hydrogenases Using Protein Film Electrochemistry. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/15001

Chicago Manual of Style (16th Edition):

Mcintosh, Chelsea Lee. “The Investigation and Characterization of the Group 3 [NiFe]-Hydrogenases Using Protein Film Electrochemistry.” 2012. Doctoral Dissertation, Arizona State University. Accessed June 19, 2019. http://repository.asu.edu/items/15001.

MLA Handbook (7th Edition):

Mcintosh, Chelsea Lee. “The Investigation and Characterization of the Group 3 [NiFe]-Hydrogenases Using Protein Film Electrochemistry.” 2012. Web. 19 Jun 2019.

Vancouver:

Mcintosh CL. The Investigation and Characterization of the Group 3 [NiFe]-Hydrogenases Using Protein Film Electrochemistry. [Internet] [Doctoral dissertation]. Arizona State University; 2012. [cited 2019 Jun 19]. Available from: http://repository.asu.edu/items/15001.

Council of Science Editors:

Mcintosh CL. The Investigation and Characterization of the Group 3 [NiFe]-Hydrogenases Using Protein Film Electrochemistry. [Doctoral Dissertation]. Arizona State University; 2012. Available from: http://repository.asu.edu/items/15001

17. Nakano, Asuka. Protein Dielectrophoresis Using Insulator-based Microfluidic Platforms.

Degree: PhD, Chemistry, 2014, Arizona State University

 Rapid and reliable separation and analysis of proteins require powerful analytical methods. The analysis of proteins becomes especially challenging when only small sample volumes are… (more)

Subjects/Keywords: Chemistry; Biochemistry; Dielectrophoresis; Lab-on-a-chip; Microfluidics; Pre-concentration; Protein; Separation

…66 6 PROTEIN INSULATOR BASED DIELECTROPHORESIS WITH NANOCONSTRICTION DEVICES… …INFLUENCING PROTEIN DIELECTROPHORESIS UNDER DC CONDITIONS… …Potential Dependency on Protein Concentration .....................77 Theoretical Considerations… …viii CHAPTER Page Extension of Protein iDEP Studies to Biomarker Separations… …156 ix LIST OF TABLES TABLE Page 2-1 Fundamental studies of peptide and protein DEP… 

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APA (6th Edition):

Nakano, A. (2014). Protein Dielectrophoresis Using Insulator-based Microfluidic Platforms. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/24979

Chicago Manual of Style (16th Edition):

Nakano, Asuka. “Protein Dielectrophoresis Using Insulator-based Microfluidic Platforms.” 2014. Doctoral Dissertation, Arizona State University. Accessed June 19, 2019. http://repository.asu.edu/items/24979.

MLA Handbook (7th Edition):

Nakano, Asuka. “Protein Dielectrophoresis Using Insulator-based Microfluidic Platforms.” 2014. Web. 19 Jun 2019.

Vancouver:

Nakano A. Protein Dielectrophoresis Using Insulator-based Microfluidic Platforms. [Internet] [Doctoral dissertation]. Arizona State University; 2014. [cited 2019 Jun 19]. Available from: http://repository.asu.edu/items/24979.

Council of Science Editors:

Nakano A. Protein Dielectrophoresis Using Insulator-based Microfluidic Platforms. [Doctoral Dissertation]. Arizona State University; 2014. Available from: http://repository.asu.edu/items/24979

18. Kwan, Patrick. The Investigation and Characterization of Redox Enzymes Using Protein Film Electrochemistry.

Degree: Biochemistry, 2014, Arizona State University

Subjects/Keywords: Biochemistry; Chemistry; Inorganic chemistry; Antimony Tin Oxide; Catalytic Bias; Hydrogenase; Oxygen Tolerance; Protein Film Electrochemistry; Pyrococcus furiosus

…LIST OF FIGURES Figure Page 1-1 Schematic of Protein Film Electrochemistry and Ideal… …Morpholino]Ethane-Sulfonic Acid PEG Polyethylene Glycol PFE Protein Film Electrochemistry… …Introduction: A Primer on Protein Film Electrochemistry, Transparent Conducting Oxides, Hydrogenases… …and Overview of This Dissertation Patrick Kwan and Anne K. Jones Department of Chemistry… …and Biochemistry, Arizona State University, Tempe, AZ 85287 1 Redox Proteins and Protein… 

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APA (6th Edition):

Kwan, P. (2014). The Investigation and Characterization of Redox Enzymes Using Protein Film Electrochemistry. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/26871

Chicago Manual of Style (16th Edition):

Kwan, Patrick. “The Investigation and Characterization of Redox Enzymes Using Protein Film Electrochemistry.” 2014. Doctoral Dissertation, Arizona State University. Accessed June 19, 2019. http://repository.asu.edu/items/26871.

MLA Handbook (7th Edition):

Kwan, Patrick. “The Investigation and Characterization of Redox Enzymes Using Protein Film Electrochemistry.” 2014. Web. 19 Jun 2019.

Vancouver:

Kwan P. The Investigation and Characterization of Redox Enzymes Using Protein Film Electrochemistry. [Internet] [Doctoral dissertation]. Arizona State University; 2014. [cited 2019 Jun 19]. Available from: http://repository.asu.edu/items/26871.

Council of Science Editors:

Kwan P. The Investigation and Characterization of Redox Enzymes Using Protein Film Electrochemistry. [Doctoral Dissertation]. Arizona State University; 2014. Available from: http://repository.asu.edu/items/26871

19. Xu, Dian. Elucidating the Molecular Dynamics, Structure and Assembly of Spider Dragline Silk Proteins by Nuclear Magnetic Resonance (NMR) Spectroscopy.

Degree: Chemistry, 2015, Arizona State University

Subjects/Keywords: Chemistry; Biophysics; Analytical chemistry; Intrinsic Disordered Protein; NMR; Protein Dynamics; Protein Structure; Self Assembly; Spider Silk

…1.3. 2D 1H-15N HSQC NMR Spectrum of the Uniformly 13C, 15N Labeled Protein GB1 Domain… …Kinetic Curves of the Silk Protein Assembly at pH = 4 with Static and 4 kHz MAS Conditions… …103 4.8. Partial Primary Amino Acid Sequence for the Peucetia viridans Spider MaSp1 Protein… …Concentration for Silk Protein in 4 M Urea… …42 3.1. 13 C Chemical Shift of Native Black Widow MA Gland Protein before and after… 

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APA (6th Edition):

Xu, D. (2015). Elucidating the Molecular Dynamics, Structure and Assembly of Spider Dragline Silk Proteins by Nuclear Magnetic Resonance (NMR) Spectroscopy. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/29769

Chicago Manual of Style (16th Edition):

Xu, Dian. “Elucidating the Molecular Dynamics, Structure and Assembly of Spider Dragline Silk Proteins by Nuclear Magnetic Resonance (NMR) Spectroscopy.” 2015. Doctoral Dissertation, Arizona State University. Accessed June 19, 2019. http://repository.asu.edu/items/29769.

MLA Handbook (7th Edition):

Xu, Dian. “Elucidating the Molecular Dynamics, Structure and Assembly of Spider Dragline Silk Proteins by Nuclear Magnetic Resonance (NMR) Spectroscopy.” 2015. Web. 19 Jun 2019.

Vancouver:

Xu D. Elucidating the Molecular Dynamics, Structure and Assembly of Spider Dragline Silk Proteins by Nuclear Magnetic Resonance (NMR) Spectroscopy. [Internet] [Doctoral dissertation]. Arizona State University; 2015. [cited 2019 Jun 19]. Available from: http://repository.asu.edu/items/29769.

Council of Science Editors:

Xu D. Elucidating the Molecular Dynamics, Structure and Assembly of Spider Dragline Silk Proteins by Nuclear Magnetic Resonance (NMR) Spectroscopy. [Doctoral Dissertation]. Arizona State University; 2015. Available from: http://repository.asu.edu/items/29769

20. Smiles, William J. Autophagy and Protein Turnover Responses to Exercise-Nutrient Interactions in Human Skeletal Muscle.

Degree: PhD, 2017, Australian Catholic University

  Skeletal muscle is a dynamic tissue comprising the largest protein reservoir of the human body with a rate of turnover of ~1-2% per day.… (more)

Subjects/Keywords: autophagy; exercise; nutrient; protein; skeletal muscle; Amino Acids, Peptides, and Proteins; Biochemical Phenomena, Metabolism, and Nutrition; Medical Sciences; Medicine and Health Sciences; Other Chemistry; Physiological Processes

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APA (6th Edition):

Smiles, W. J. (2017). Autophagy and Protein Turnover Responses to Exercise-Nutrient Interactions in Human Skeletal Muscle. (Doctoral Dissertation). Australian Catholic University. Retrieved from https://researchbank.acu.edu.au/theses/649

Chicago Manual of Style (16th Edition):

Smiles, William J. “Autophagy and Protein Turnover Responses to Exercise-Nutrient Interactions in Human Skeletal Muscle.” 2017. Doctoral Dissertation, Australian Catholic University. Accessed June 19, 2019. https://researchbank.acu.edu.au/theses/649.

MLA Handbook (7th Edition):

Smiles, William J. “Autophagy and Protein Turnover Responses to Exercise-Nutrient Interactions in Human Skeletal Muscle.” 2017. Web. 19 Jun 2019.

Vancouver:

Smiles WJ. Autophagy and Protein Turnover Responses to Exercise-Nutrient Interactions in Human Skeletal Muscle. [Internet] [Doctoral dissertation]. Australian Catholic University; 2017. [cited 2019 Jun 19]. Available from: https://researchbank.acu.edu.au/theses/649.

Council of Science Editors:

Smiles WJ. Autophagy and Protein Turnover Responses to Exercise-Nutrient Interactions in Human Skeletal Muscle. [Doctoral Dissertation]. Australian Catholic University; 2017. Available from: https://researchbank.acu.edu.au/theses/649


Australian National University

21. Terrett, Richard Norman Leslie. Computational Investigation of the Oxygen Evolving Complex of Photosystem II and Related Models via Density Functional Theory .

Degree: 2017, Australian National University

 The first step of photosynthetic metabolism effects the facile oxidation of water to dioxygen and hydrogen cations. This is achieved through an incompletely-understood process of… (more)

Subjects/Keywords: Photosynthesis; Photosystem II; Density Functional Theory; Computational Chemistry; Quantum Chemistry; Theoretical Chemistry; Electronic Structure; Molecular Structure; Biomimesis; Bioinorganic Chemistry; Vibrational Structure; Mobile Block Hessian; Infrared Difference Spectroscopy; Hyperfine Interaction; Magnetic Structure; Superexchange Interaction; Protein; Metalloprotein; Enzyme; Joliot-Kok Cycle; Artificial Photosynthesis; Water Oxidation; Water Splitting; Renewable Energy; Green Energy; Proton-Coupled Electron Transfer; Oxygen Evolving Complex; Water Oxidising Complex; Water Oxidizing Complex; Chloroplast; Thylakoid Membrane; Forster Resonance

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APA (6th Edition):

Terrett, R. N. L. (2017). Computational Investigation of the Oxygen Evolving Complex of Photosystem II and Related Models via Density Functional Theory . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/133592

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

Chicago Manual of Style (16th Edition):

Terrett, Richard Norman Leslie. “Computational Investigation of the Oxygen Evolving Complex of Photosystem II and Related Models via Density Functional Theory .” 2017. Thesis, Australian National University. Accessed June 19, 2019. http://hdl.handle.net/1885/133592.

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

MLA Handbook (7th Edition):

Terrett, Richard Norman Leslie. “Computational Investigation of the Oxygen Evolving Complex of Photosystem II and Related Models via Density Functional Theory .” 2017. Web. 19 Jun 2019.

Vancouver:

Terrett RNL. Computational Investigation of the Oxygen Evolving Complex of Photosystem II and Related Models via Density Functional Theory . [Internet] [Thesis]. Australian National University; 2017. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/1885/133592.

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

Council of Science Editors:

Terrett RNL. Computational Investigation of the Oxygen Evolving Complex of Photosystem II and Related Models via Density Functional Theory . [Thesis]. Australian National University; 2017. Available from: http://hdl.handle.net/1885/133592

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

22. Dauvergne, Julien. Synthèse et étude physico-chimique de nouveaux tensioactifs utilisables pour la cristallisation 2D sur film lipidique et l’étude des protéines membranaires : Synthesis and physico-chemical study of new surfactants used as tools for the cristallisation 2D on lipidic film and manipulation of membrane proteins.

Degree: Docteur es, Chimie, 2010, Avignon

Ce manuscrit décrit la synthèse et l’étude physico-chimique de tensioactifs innovants utilisés comme outils biochimiques pour le maintien et la cristallisation de protéines membranaires en… (more)

Subjects/Keywords: Protéine membranaire; Tensioactif hémifluoré; Amphiphile facial; Click chemistry; Cristallisation 2D; Tensiométrie; Aromatique persubstitué; Membrane protein; Hemifluorinated surfactant; Facial amphiphile; Click chemistry; Crystallisation 2D; Tensiometry; Aromatic persubstitued

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APA (6th Edition):

Dauvergne, J. (2010). Synthèse et étude physico-chimique de nouveaux tensioactifs utilisables pour la cristallisation 2D sur film lipidique et l’étude des protéines membranaires : Synthesis and physico-chemical study of new surfactants used as tools for the cristallisation 2D on lipidic film and manipulation of membrane proteins. (Doctoral Dissertation). Avignon. Retrieved from http://www.theses.fr/2010AVIG0233

Chicago Manual of Style (16th Edition):

Dauvergne, Julien. “Synthèse et étude physico-chimique de nouveaux tensioactifs utilisables pour la cristallisation 2D sur film lipidique et l’étude des protéines membranaires : Synthesis and physico-chemical study of new surfactants used as tools for the cristallisation 2D on lipidic film and manipulation of membrane proteins.” 2010. Doctoral Dissertation, Avignon. Accessed June 19, 2019. http://www.theses.fr/2010AVIG0233.

MLA Handbook (7th Edition):

Dauvergne, Julien. “Synthèse et étude physico-chimique de nouveaux tensioactifs utilisables pour la cristallisation 2D sur film lipidique et l’étude des protéines membranaires : Synthesis and physico-chemical study of new surfactants used as tools for the cristallisation 2D on lipidic film and manipulation of membrane proteins.” 2010. Web. 19 Jun 2019.

Vancouver:

Dauvergne J. Synthèse et étude physico-chimique de nouveaux tensioactifs utilisables pour la cristallisation 2D sur film lipidique et l’étude des protéines membranaires : Synthesis and physico-chemical study of new surfactants used as tools for the cristallisation 2D on lipidic film and manipulation of membrane proteins. [Internet] [Doctoral dissertation]. Avignon; 2010. [cited 2019 Jun 19]. Available from: http://www.theses.fr/2010AVIG0233.

Council of Science Editors:

Dauvergne J. Synthèse et étude physico-chimique de nouveaux tensioactifs utilisables pour la cristallisation 2D sur film lipidique et l’étude des protéines membranaires : Synthesis and physico-chemical study of new surfactants used as tools for the cristallisation 2D on lipidic film and manipulation of membrane proteins. [Doctoral Dissertation]. Avignon; 2010. Available from: http://www.theses.fr/2010AVIG0233


Boise State University

23. Elsberg, Josiah G. The Effects of Hydrogen Bonding on the Reactivity of Synthetic Ada Repair Protein Analogues.

Degree: 2016, Boise State University

 The study of bioinorganic chemistry is an important field, as it can provide insight as to why Nature has chosen certain active sites and structures… (more)

Subjects/Keywords: synthetic analogues; ada repair protein; hydrogen bonding; zinc; secondary coordination sphere; thiolate; Inorganic Chemistry; Organic Chemistry; Physical Chemistry

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APA (6th Edition):

Elsberg, J. G. (2016). The Effects of Hydrogen Bonding on the Reactivity of Synthetic Ada Repair Protein Analogues. (Thesis). Boise State University. Retrieved from https://scholarworks.boisestate.edu/td/1101

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

Chicago Manual of Style (16th Edition):

Elsberg, Josiah G. “The Effects of Hydrogen Bonding on the Reactivity of Synthetic Ada Repair Protein Analogues.” 2016. Thesis, Boise State University. Accessed June 19, 2019. https://scholarworks.boisestate.edu/td/1101.

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

MLA Handbook (7th Edition):

Elsberg, Josiah G. “The Effects of Hydrogen Bonding on the Reactivity of Synthetic Ada Repair Protein Analogues.” 2016. Web. 19 Jun 2019.

Vancouver:

Elsberg JG. The Effects of Hydrogen Bonding on the Reactivity of Synthetic Ada Repair Protein Analogues. [Internet] [Thesis]. Boise State University; 2016. [cited 2019 Jun 19]. Available from: https://scholarworks.boisestate.edu/td/1101.

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

Council of Science Editors:

Elsberg JG. The Effects of Hydrogen Bonding on the Reactivity of Synthetic Ada Repair Protein Analogues. [Thesis]. Boise State University; 2016. Available from: https://scholarworks.boisestate.edu/td/1101

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


Boise State University

24. Cornell, Nicole. Molecular Basis of Substrate Recognition in BjaI, an AHL Synthase from Bradyrhizobium Japonicum.

Degree: 2017, Boise State University

 Resistance to antibiotics has become a major challenge in today’s society for treating bacterial infections. Inhibition of quorum sensing has a potential to be a… (more)

Subjects/Keywords: enzyme kinetics; inhibition; acyl-acyl carrier protein; acyl-coenzyme A; Chemistry; Medicinal-Pharmaceutical Chemistry; Physical Sciences and Mathematics

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APA (6th Edition):

Cornell, N. (2017). Molecular Basis of Substrate Recognition in BjaI, an AHL Synthase from Bradyrhizobium Japonicum. (Thesis). Boise State University. Retrieved from https://scholarworks.boisestate.edu/td/1247

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

Chicago Manual of Style (16th Edition):

Cornell, Nicole. “Molecular Basis of Substrate Recognition in BjaI, an AHL Synthase from Bradyrhizobium Japonicum.” 2017. Thesis, Boise State University. Accessed June 19, 2019. https://scholarworks.boisestate.edu/td/1247.

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

MLA Handbook (7th Edition):

Cornell, Nicole. “Molecular Basis of Substrate Recognition in BjaI, an AHL Synthase from Bradyrhizobium Japonicum.” 2017. Web. 19 Jun 2019.

Vancouver:

Cornell N. Molecular Basis of Substrate Recognition in BjaI, an AHL Synthase from Bradyrhizobium Japonicum. [Internet] [Thesis]. Boise State University; 2017. [cited 2019 Jun 19]. Available from: https://scholarworks.boisestate.edu/td/1247.

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

Council of Science Editors:

Cornell N. Molecular Basis of Substrate Recognition in BjaI, an AHL Synthase from Bradyrhizobium Japonicum. [Thesis]. Boise State University; 2017. Available from: https://scholarworks.boisestate.edu/td/1247

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


Boston College

25. Couvertier, Shalise Monique. Chemical-proteomic strategies to study cysteine posttranslational modifications.

Degree: PhD, Chemistry, 2016, Boston College

 Cysteine residues on proteins play important catalytic and regulatory roles in complex proteomes. These functional residues can be modified under physiological conditions by posttranslational modifications… (more)

Subjects/Keywords: Activity-based Protein Profiling; Chemical Biology; Chemistry; Cysteine; Probe Development; Proteomics

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APA (6th Edition):

Couvertier, S. M. (2016). Chemical-proteomic strategies to study cysteine posttranslational modifications. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:107200

Chicago Manual of Style (16th Edition):

Couvertier, Shalise Monique. “Chemical-proteomic strategies to study cysteine posttranslational modifications.” 2016. Doctoral Dissertation, Boston College. Accessed June 19, 2019. http://dlib.bc.edu/islandora/object/bc-ir:107200.

MLA Handbook (7th Edition):

Couvertier, Shalise Monique. “Chemical-proteomic strategies to study cysteine posttranslational modifications.” 2016. Web. 19 Jun 2019.

Vancouver:

Couvertier SM. Chemical-proteomic strategies to study cysteine posttranslational modifications. [Internet] [Doctoral dissertation]. Boston College; 2016. [cited 2019 Jun 19]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107200.

Council of Science Editors:

Couvertier SM. Chemical-proteomic strategies to study cysteine posttranslational modifications. [Doctoral Dissertation]. Boston College; 2016. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107200

26. Foster, Leigh Suzanne Holmes. The effect of sequence and environment on the structure and dimerization of amyloid precursor protein.

Degree: PhD, Chemistry, 2015, Boston University

 Aggregation of amyloid β (Aβ) protein has been linked to the development of Alzheimer's Disease (AD). The genesis of Aβ involves the cleavage Amyloid Precursor… (more)

Subjects/Keywords: Chemistry; Computational chemistry; Molecular dynamics; Protein structure

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APA (6th Edition):

Foster, L. S. H. (2015). The effect of sequence and environment on the structure and dimerization of amyloid precursor protein. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/15180

Chicago Manual of Style (16th Edition):

Foster, Leigh Suzanne Holmes. “The effect of sequence and environment on the structure and dimerization of amyloid precursor protein.” 2015. Doctoral Dissertation, Boston University. Accessed June 19, 2019. http://hdl.handle.net/2144/15180.

MLA Handbook (7th Edition):

Foster, Leigh Suzanne Holmes. “The effect of sequence and environment on the structure and dimerization of amyloid precursor protein.” 2015. Web. 19 Jun 2019.

Vancouver:

Foster LSH. The effect of sequence and environment on the structure and dimerization of amyloid precursor protein. [Internet] [Doctoral dissertation]. Boston University; 2015. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/2144/15180.

Council of Science Editors:

Foster LSH. The effect of sequence and environment on the structure and dimerization of amyloid precursor protein. [Doctoral Dissertation]. Boston University; 2015. Available from: http://hdl.handle.net/2144/15180


Boston University

27. Xu, Xiaobin. Mass spectrometry approaches for profiling protein-protein interactions.

Degree: PhD, Chemistry, 2014, Boston University

 This dissertation is focused on developing cross-linking and mass spectrometry methodologies to study protein-protein interactions. Top-down cross-linking, in combination with mass spectrometry, provides advantages over… (more)

Subjects/Keywords: Analytical chemistry; Aggresome; Synphilin-1; Top-down; Chemical cross-linking; Mass spectrometry; Protein interaction

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APA (6th Edition):

Xu, X. (2014). Mass spectrometry approaches for profiling protein-protein interactions. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/14097

Chicago Manual of Style (16th Edition):

Xu, Xiaobin. “Mass spectrometry approaches for profiling protein-protein interactions.” 2014. Doctoral Dissertation, Boston University. Accessed June 19, 2019. http://hdl.handle.net/2144/14097.

MLA Handbook (7th Edition):

Xu, Xiaobin. “Mass spectrometry approaches for profiling protein-protein interactions.” 2014. Web. 19 Jun 2019.

Vancouver:

Xu X. Mass spectrometry approaches for profiling protein-protein interactions. [Internet] [Doctoral dissertation]. Boston University; 2014. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/2144/14097.

Council of Science Editors:

Xu X. Mass spectrometry approaches for profiling protein-protein interactions. [Doctoral Dissertation]. Boston University; 2014. Available from: http://hdl.handle.net/2144/14097


Boston University

28. Soltau, Sarah Rose. Studies toward the mechanism of allosteric activation in phenylalanine hydroxylase.

Degree: PhD, Chemistry, 2014, Boston University

 Phenylalanine hydroxylase (PAH, EC: 1.14.16.1) is a non-heme iron tetrahydropterin-dependent monooxygenase that maintains phenylalanine (L-Phe) homeostasis via conversion of L-Phe to L-Tyr. PAH is an… (more)

Subjects/Keywords: Chemistry; Allostery; Conformational change; Enzymes; Protein; Stopped flow fluorescence; Surface acoustic wave biosensing

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APA (6th Edition):

Soltau, S. R. (2014). Studies toward the mechanism of allosteric activation in phenylalanine hydroxylase. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/14146

Chicago Manual of Style (16th Edition):

Soltau, Sarah Rose. “Studies toward the mechanism of allosteric activation in phenylalanine hydroxylase.” 2014. Doctoral Dissertation, Boston University. Accessed June 19, 2019. http://hdl.handle.net/2144/14146.

MLA Handbook (7th Edition):

Soltau, Sarah Rose. “Studies toward the mechanism of allosteric activation in phenylalanine hydroxylase.” 2014. Web. 19 Jun 2019.

Vancouver:

Soltau SR. Studies toward the mechanism of allosteric activation in phenylalanine hydroxylase. [Internet] [Doctoral dissertation]. Boston University; 2014. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/2144/14146.

Council of Science Editors:

Soltau SR. Studies toward the mechanism of allosteric activation in phenylalanine hydroxylase. [Doctoral Dissertation]. Boston University; 2014. Available from: http://hdl.handle.net/2144/14146


Boston University

29. Villar, Elizabeth A. Study of protein-macrocycle Interactions for lessons in drug design.

Degree: PhD, Chemistry, 2016, Boston University

 Macrocycles (MCs) have become an increasing area of interest for drug design efforts, especially for classically “difficult” targets like protein-protein interactions (PPIs). And although there… (more)

Subjects/Keywords: Chemistry; Drug design; Macrocycle; NEMO; Protein mapping

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

APA (6th Edition):

Villar, E. A. (2016). Study of protein-macrocycle Interactions for lessons in drug design. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/19759

Chicago Manual of Style (16th Edition):

Villar, Elizabeth A. “Study of protein-macrocycle Interactions for lessons in drug design.” 2016. Doctoral Dissertation, Boston University. Accessed June 19, 2019. http://hdl.handle.net/2144/19759.

MLA Handbook (7th Edition):

Villar, Elizabeth A. “Study of protein-macrocycle Interactions for lessons in drug design.” 2016. Web. 19 Jun 2019.

Vancouver:

Villar EA. Study of protein-macrocycle Interactions for lessons in drug design. [Internet] [Doctoral dissertation]. Boston University; 2016. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/2144/19759.

Council of Science Editors:

Villar EA. Study of protein-macrocycle Interactions for lessons in drug design. [Doctoral Dissertation]. Boston University; 2016. Available from: http://hdl.handle.net/2144/19759


Boston University

30. Levin, Benjamin Diamon. Probing the structure-function relationship of heme c containing bacterial proteins: monoheme cytochromes c and diheme cytochrome c peroxidase.

Degree: PhD, Chemistry, 2013, Boston University

 Heme containing proteins and their reactivity play a central role in biological systems; they have a vast range of functions including electron transfer, catalysis, and… (more)

Subjects/Keywords: Chemistry; Cyclic voltammetry; Cytochrome c; Diheme peroxidase; Protein film voltammetry

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

APA (6th Edition):

Levin, B. D. (2013). Probing the structure-function relationship of heme c containing bacterial proteins: monoheme cytochromes c and diheme cytochrome c peroxidase. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/14093

Chicago Manual of Style (16th Edition):

Levin, Benjamin Diamon. “Probing the structure-function relationship of heme c containing bacterial proteins: monoheme cytochromes c and diheme cytochrome c peroxidase.” 2013. Doctoral Dissertation, Boston University. Accessed June 19, 2019. http://hdl.handle.net/2144/14093.

MLA Handbook (7th Edition):

Levin, Benjamin Diamon. “Probing the structure-function relationship of heme c containing bacterial proteins: monoheme cytochromes c and diheme cytochrome c peroxidase.” 2013. Web. 19 Jun 2019.

Vancouver:

Levin BD. Probing the structure-function relationship of heme c containing bacterial proteins: monoheme cytochromes c and diheme cytochrome c peroxidase. [Internet] [Doctoral dissertation]. Boston University; 2013. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/2144/14093.

Council of Science Editors:

Levin BD. Probing the structure-function relationship of heme c containing bacterial proteins: monoheme cytochromes c and diheme cytochrome c peroxidase. [Doctoral Dissertation]. Boston University; 2013. Available from: http://hdl.handle.net/2144/14093

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