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You searched for subject:(Protein chemistry). Showing records 1 – 30 of 783 total matches.

[1] [2] [3] [4] [5] … [27]

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University of California – San Diego

1. Kozachenko, Ivan Andrew. Studies of Membrane Protein Folding by Bimolecular Fluorescence Quenching.

Degree: Chemistry, 2016, University of California – San Diego

 This project investigates changes in protein solvation during the folding reaction of Outer membrane protein A (OmpA) of Escherichia Coli, and correlates this dehydration process… (more)

Subjects/Keywords: Biophysics; Chemistry; membrane protein; protein; protein folding

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

APA (6th Edition):

Kozachenko, I. A. (2016). Studies of Membrane Protein Folding by Bimolecular Fluorescence Quenching. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/6wh40797

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):

Kozachenko, Ivan Andrew. “Studies of Membrane Protein Folding by Bimolecular Fluorescence Quenching.” 2016. Thesis, University of California – San Diego. Accessed June 19, 2019. http://www.escholarship.org/uc/item/6wh40797.

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

MLA Handbook (7th Edition):

Kozachenko, Ivan Andrew. “Studies of Membrane Protein Folding by Bimolecular Fluorescence Quenching.” 2016. Web. 19 Jun 2019.

Vancouver:

Kozachenko IA. Studies of Membrane Protein Folding by Bimolecular Fluorescence Quenching. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2019 Jun 19]. Available from: http://www.escholarship.org/uc/item/6wh40797.

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

Council of Science Editors:

Kozachenko IA. Studies of Membrane Protein Folding by Bimolecular Fluorescence Quenching. [Thesis]. University of California – San Diego; 2016. Available from: http://www.escholarship.org/uc/item/6wh40797

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


University of New Mexico

2. Bryan, Tyrel. Criteria for Evolution of Successful Proteins: Fold Fitness and Domain Dynamics Explored.

Degree: Department of Chemistry and Chemical Biology, 2014, University of New Mexico

  The Haloacid Dehalogenase Superfamily (HADSF) is a ubiquitous family of enzyme with more than 32,000 members. A variety of reactions are catalyzed by HAD… (more)

Subjects/Keywords: Protein Folding; Chemistry; Physical Chemistry

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APA (6th Edition):

Bryan, T. (2014). Criteria for Evolution of Successful Proteins: Fold Fitness and Domain Dynamics Explored. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/chem_etds/35

Chicago Manual of Style (16th Edition):

Bryan, Tyrel. “Criteria for Evolution of Successful Proteins: Fold Fitness and Domain Dynamics Explored.” 2014. Doctoral Dissertation, University of New Mexico. Accessed June 19, 2019. https://digitalrepository.unm.edu/chem_etds/35.

MLA Handbook (7th Edition):

Bryan, Tyrel. “Criteria for Evolution of Successful Proteins: Fold Fitness and Domain Dynamics Explored.” 2014. Web. 19 Jun 2019.

Vancouver:

Bryan T. Criteria for Evolution of Successful Proteins: Fold Fitness and Domain Dynamics Explored. [Internet] [Doctoral dissertation]. University of New Mexico; 2014. [cited 2019 Jun 19]. Available from: https://digitalrepository.unm.edu/chem_etds/35.

Council of Science Editors:

Bryan T. Criteria for Evolution of Successful Proteins: Fold Fitness and Domain Dynamics Explored. [Doctoral Dissertation]. University of New Mexico; 2014. Available from: https://digitalrepository.unm.edu/chem_etds/35


University of New Mexico

3. Toews Keating, Sarah. Mining Public Databases for Discovery of Structure and Function within the Hotdog-fold Thioesterase and HAD Phosphatase Enzyme Families.

Degree: Department of Chemistry and Chemical Biology, 2015, University of New Mexico

  For my doctoral work, I have developed strategies to mine public databases for data that can be used to infer structural and functional information… (more)

Subjects/Keywords: Chemistry; Bioinformatics; Protein evolution; Chemistry; Physical Chemistry

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APA (6th Edition):

Toews Keating, S. (2015). Mining Public Databases for Discovery of Structure and Function within the Hotdog-fold Thioesterase and HAD Phosphatase Enzyme Families. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/chem_etds/23

Chicago Manual of Style (16th Edition):

Toews Keating, Sarah. “Mining Public Databases for Discovery of Structure and Function within the Hotdog-fold Thioesterase and HAD Phosphatase Enzyme Families.” 2015. Doctoral Dissertation, University of New Mexico. Accessed June 19, 2019. https://digitalrepository.unm.edu/chem_etds/23.

MLA Handbook (7th Edition):

Toews Keating, Sarah. “Mining Public Databases for Discovery of Structure and Function within the Hotdog-fold Thioesterase and HAD Phosphatase Enzyme Families.” 2015. Web. 19 Jun 2019.

Vancouver:

Toews Keating S. Mining Public Databases for Discovery of Structure and Function within the Hotdog-fold Thioesterase and HAD Phosphatase Enzyme Families. [Internet] [Doctoral dissertation]. University of New Mexico; 2015. [cited 2019 Jun 19]. Available from: https://digitalrepository.unm.edu/chem_etds/23.

Council of Science Editors:

Toews Keating S. Mining Public Databases for Discovery of Structure and Function within the Hotdog-fold Thioesterase and HAD Phosphatase Enzyme Families. [Doctoral Dissertation]. University of New Mexico; 2015. Available from: https://digitalrepository.unm.edu/chem_etds/23


University of Arizona

4. Kumirov, Vlad K. Mechanisms and Consequences of Evolving a New Protein Fold .

Degree: 2016, University of Arizona

 The ability of mutations to change the fold of a protein provides evolutionary pathways to new structures. To study hypothetical pathways for protein fold evolution,… (more)

Subjects/Keywords: protein fold transformation; protein nmr spectroscopy; protein structure; Chemistry; protein evolution

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APA (6th Edition):

Kumirov, V. K. (2016). Mechanisms and Consequences of Evolving a New Protein Fold . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/605218

Chicago Manual of Style (16th Edition):

Kumirov, Vlad K. “Mechanisms and Consequences of Evolving a New Protein Fold .” 2016. Doctoral Dissertation, University of Arizona. Accessed June 19, 2019. http://hdl.handle.net/10150/605218.

MLA Handbook (7th Edition):

Kumirov, Vlad K. “Mechanisms and Consequences of Evolving a New Protein Fold .” 2016. Web. 19 Jun 2019.

Vancouver:

Kumirov VK. Mechanisms and Consequences of Evolving a New Protein Fold . [Internet] [Doctoral dissertation]. University of Arizona; 2016. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/10150/605218.

Council of Science Editors:

Kumirov VK. Mechanisms and Consequences of Evolving a New Protein Fold . [Doctoral Dissertation]. University of Arizona; 2016. Available from: http://hdl.handle.net/10150/605218


University of Rochester

5. Park, Min Sun. Computational Studies of Proteins: Dynamics and Interactions with Small Molecules.

Degree: PhD, 2011, University of Rochester

 Understanding protein dynamics is important for drug design. G proteins play an important role in cellular signal transduction and are involved in many processes. They… (more)

Subjects/Keywords: Computational Chemistry; Virtual Screening; Protein-Protein Interaction

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APA (6th Edition):

Park, M. S. (2011). Computational Studies of Proteins: Dynamics and Interactions with Small Molecules. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/15859

Chicago Manual of Style (16th Edition):

Park, Min Sun. “Computational Studies of Proteins: Dynamics and Interactions with Small Molecules.” 2011. Doctoral Dissertation, University of Rochester. Accessed June 19, 2019. http://hdl.handle.net/1802/15859.

MLA Handbook (7th Edition):

Park, Min Sun. “Computational Studies of Proteins: Dynamics and Interactions with Small Molecules.” 2011. Web. 19 Jun 2019.

Vancouver:

Park MS. Computational Studies of Proteins: Dynamics and Interactions with Small Molecules. [Internet] [Doctoral dissertation]. University of Rochester; 2011. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/1802/15859.

Council of Science Editors:

Park MS. Computational Studies of Proteins: Dynamics and Interactions with Small Molecules. [Doctoral Dissertation]. University of Rochester; 2011. Available from: http://hdl.handle.net/1802/15859


University of Michigan

6. Clark, Jordan. Structural Investigation of Binding Events in Proteins.

Degree: PhD, Medicinal Chemistry, 2018, University of Michigan

 Understanding the biophysical properties that describe protein binding events has allowed for the advancement of drug discovery through structure-based drug design and in silico methodology.… (more)

Subjects/Keywords: Protein flexibility; Protein structure database; Protein-ligand binding; Protein-protein interaction (PPI); Biological Chemistry; Science

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APA (6th Edition):

Clark, J. (2018). Structural Investigation of Binding Events in Proteins. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/145943

Chicago Manual of Style (16th Edition):

Clark, Jordan. “Structural Investigation of Binding Events in Proteins.” 2018. Doctoral Dissertation, University of Michigan. Accessed June 19, 2019. http://hdl.handle.net/2027.42/145943.

MLA Handbook (7th Edition):

Clark, Jordan. “Structural Investigation of Binding Events in Proteins.” 2018. Web. 19 Jun 2019.

Vancouver:

Clark J. Structural Investigation of Binding Events in Proteins. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/2027.42/145943.

Council of Science Editors:

Clark J. Structural Investigation of Binding Events in Proteins. [Doctoral Dissertation]. University of Michigan; 2018. Available from: http://hdl.handle.net/2027.42/145943


The Ohio State University

7. Luechapanichkul, Rinrada. Determination of the Sequence Specificity and Protein Substrates of Protein Phosphatases.

Degree: PhD, Chemistry, 2014, The Ohio State University

Protein phosphorylation is a post-translational modification controlled by two counteracting enzyme families, protein kinases and phosphatases. Protein phosphatases have been demonstrated to regulate many… (more)

Subjects/Keywords: Chemistry; protein phosphatases, sequence specificity

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APA (6th Edition):

Luechapanichkul, R. (2014). Determination of the Sequence Specificity and Protein Substrates of Protein Phosphatases. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1398868380

Chicago Manual of Style (16th Edition):

Luechapanichkul, Rinrada. “Determination of the Sequence Specificity and Protein Substrates of Protein Phosphatases.” 2014. Doctoral Dissertation, The Ohio State University. Accessed June 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1398868380.

MLA Handbook (7th Edition):

Luechapanichkul, Rinrada. “Determination of the Sequence Specificity and Protein Substrates of Protein Phosphatases.” 2014. Web. 19 Jun 2019.

Vancouver:

Luechapanichkul R. Determination of the Sequence Specificity and Protein Substrates of Protein Phosphatases. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2019 Jun 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1398868380.

Council of Science Editors:

Luechapanichkul R. Determination of the Sequence Specificity and Protein Substrates of Protein Phosphatases. [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1398868380


Michigan State University

8. Yapici, Ipek. Design of novel protein/chromophore complexes : synthesis and evaluation of chromophores, fluorophores, and engineering of protein host systems.

Degree: 2015, Michigan State University

Thesis Ph. D. Michigan State University. Chemistry - Doctor of Philosophy 2015.

The field of protein engineering has undergone phenomenal growth from its inception approximately… (more)

Subjects/Keywords: Protein engineering; Chemistry; Biochemistry

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APA (6th Edition):

Yapici, I. (2015). Design of novel protein/chromophore complexes : synthesis and evaluation of chromophores, fluorophores, and engineering of protein host systems. (Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:3199

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):

Yapici, Ipek. “Design of novel protein/chromophore complexes : synthesis and evaluation of chromophores, fluorophores, and engineering of protein host systems.” 2015. Thesis, Michigan State University. Accessed June 19, 2019. http://etd.lib.msu.edu/islandora/object/etd:3199.

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

MLA Handbook (7th Edition):

Yapici, Ipek. “Design of novel protein/chromophore complexes : synthesis and evaluation of chromophores, fluorophores, and engineering of protein host systems.” 2015. Web. 19 Jun 2019.

Vancouver:

Yapici I. Design of novel protein/chromophore complexes : synthesis and evaluation of chromophores, fluorophores, and engineering of protein host systems. [Internet] [Thesis]. Michigan State University; 2015. [cited 2019 Jun 19]. Available from: http://etd.lib.msu.edu/islandora/object/etd:3199.

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

Council of Science Editors:

Yapici I. Design of novel protein/chromophore complexes : synthesis and evaluation of chromophores, fluorophores, and engineering of protein host systems. [Thesis]. Michigan State University; 2015. Available from: http://etd.lib.msu.edu/islandora/object/etd:3199

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


University of Michigan

9. 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 19, 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. 19 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 19]. 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


Cornell University

10. Wan, Huahua. Finding A Volume Ratio of Hyaluronic Acid to Phe-Arg-Poly(ester amide)s to Form Drug-Delivering Nanoparticle Micelles and Preliminary Drug Loading Result .

Degree: 2018, Cornell University

 Pseudo-protein is a name used to describe an amino acid based poly(ester amide)s (aa-PEA). One possible application of pseudo-protein is as a drug delivery coating.To… (more)

Subjects/Keywords: Pseudo-protein; nanoparticle; Chemistry

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APA (6th Edition):

Wan, H. (2018). Finding A Volume Ratio of Hyaluronic Acid to Phe-Arg-Poly(ester amide)s to Form Drug-Delivering Nanoparticle Micelles and Preliminary Drug Loading Result . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/64991

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):

Wan, Huahua. “Finding A Volume Ratio of Hyaluronic Acid to Phe-Arg-Poly(ester amide)s to Form Drug-Delivering Nanoparticle Micelles and Preliminary Drug Loading Result .” 2018. Thesis, Cornell University. Accessed June 19, 2019. http://hdl.handle.net/1813/64991.

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

MLA Handbook (7th Edition):

Wan, Huahua. “Finding A Volume Ratio of Hyaluronic Acid to Phe-Arg-Poly(ester amide)s to Form Drug-Delivering Nanoparticle Micelles and Preliminary Drug Loading Result .” 2018. Web. 19 Jun 2019.

Vancouver:

Wan H. Finding A Volume Ratio of Hyaluronic Acid to Phe-Arg-Poly(ester amide)s to Form Drug-Delivering Nanoparticle Micelles and Preliminary Drug Loading Result . [Internet] [Thesis]. Cornell University; 2018. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/1813/64991.

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

Council of Science Editors:

Wan H. Finding A Volume Ratio of Hyaluronic Acid to Phe-Arg-Poly(ester amide)s to Form Drug-Delivering Nanoparticle Micelles and Preliminary Drug Loading Result . [Thesis]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/64991

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


University of California – Irvine

11. Manuel, Gerald Paulo. Development of Protein Microarray Fabrication Methods for Analysis by Surface Plasmon Resonance Imaging.

Degree: Chemistry, 2017, University of California – Irvine

 This dissertation is the culmination of work toward the development of protein microarrays for surface plasmon resonance imaging (SPRI). Two main issues with protein microarrays… (more)

Subjects/Keywords: Analytical chemistry; Chemistry; Microarray; Protein; SPRI

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APA (6th Edition):

Manuel, G. P. (2017). Development of Protein Microarray Fabrication Methods for Analysis by Surface Plasmon Resonance Imaging. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/5hb0k3jr

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):

Manuel, Gerald Paulo. “Development of Protein Microarray Fabrication Methods for Analysis by Surface Plasmon Resonance Imaging.” 2017. Thesis, University of California – Irvine. Accessed June 19, 2019. http://www.escholarship.org/uc/item/5hb0k3jr.

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

MLA Handbook (7th Edition):

Manuel, Gerald Paulo. “Development of Protein Microarray Fabrication Methods for Analysis by Surface Plasmon Resonance Imaging.” 2017. Web. 19 Jun 2019.

Vancouver:

Manuel GP. Development of Protein Microarray Fabrication Methods for Analysis by Surface Plasmon Resonance Imaging. [Internet] [Thesis]. University of California – Irvine; 2017. [cited 2019 Jun 19]. Available from: http://www.escholarship.org/uc/item/5hb0k3jr.

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

Council of Science Editors:

Manuel GP. Development of Protein Microarray Fabrication Methods for Analysis by Surface Plasmon Resonance Imaging. [Thesis]. University of California – Irvine; 2017. Available from: http://www.escholarship.org/uc/item/5hb0k3jr

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

12. 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


University of Michigan

13. Govindarajoo, Brandon. Template Based Modeling and Structural Refinement of Protein-Protein Interactions.

Degree: PhD, Bioinformatics, 2016, University of Michigan

 Determining protein structures from sequence is a fundamental problem in molecular biology, as protein structure is essential to understanding protein function. In this study, I… (more)

Subjects/Keywords: Protein structure prediction.; Protein protein interactions.; Biological Chemistry; Science

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APA (6th Edition):

Govindarajoo, B. (2016). Template Based Modeling and Structural Refinement of Protein-Protein Interactions. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/135847

Chicago Manual of Style (16th Edition):

Govindarajoo, Brandon. “Template Based Modeling and Structural Refinement of Protein-Protein Interactions.” 2016. Doctoral Dissertation, University of Michigan. Accessed June 19, 2019. http://hdl.handle.net/2027.42/135847.

MLA Handbook (7th Edition):

Govindarajoo, Brandon. “Template Based Modeling and Structural Refinement of Protein-Protein Interactions.” 2016. Web. 19 Jun 2019.

Vancouver:

Govindarajoo B. Template Based Modeling and Structural Refinement of Protein-Protein Interactions. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/2027.42/135847.

Council of Science Editors:

Govindarajoo B. Template Based Modeling and Structural Refinement of Protein-Protein Interactions. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/135847


University of California – San Diego

14. Maniaci, Brian M. Design of Metal-Controlled Protein-Protein Interactions.

Degree: Chemistry and Biochemistry, 2019, University of California – San Diego

 The field of protein design strives to engineer new molecules that interact in a specific, controlled manner to form novel functional complexes. Engineered proteins that… (more)

Subjects/Keywords: Chemistry; Biochemistry; Biomaterials; Metal-Controlled Protein Dimerization; Protein Design; Protein Engineering

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APA (6th Edition):

Maniaci, B. M. (2019). Design of Metal-Controlled Protein-Protein Interactions. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/0fc2n3qm

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):

Maniaci, Brian M. “Design of Metal-Controlled Protein-Protein Interactions.” 2019. Thesis, University of California – San Diego. Accessed June 19, 2019. http://www.escholarship.org/uc/item/0fc2n3qm.

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

MLA Handbook (7th Edition):

Maniaci, Brian M. “Design of Metal-Controlled Protein-Protein Interactions.” 2019. Web. 19 Jun 2019.

Vancouver:

Maniaci BM. Design of Metal-Controlled Protein-Protein Interactions. [Internet] [Thesis]. University of California – San Diego; 2019. [cited 2019 Jun 19]. Available from: http://www.escholarship.org/uc/item/0fc2n3qm.

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

Council of Science Editors:

Maniaci BM. Design of Metal-Controlled Protein-Protein Interactions. [Thesis]. University of California – San Diego; 2019. Available from: http://www.escholarship.org/uc/item/0fc2n3qm

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


University of California – Berkeley

15. Palla, Kanwal. Development and Applications of N-terminal Protein Bioconjugation Reactions.

Degree: Chemistry, 2016, University of California – Berkeley

 With highly evolved structures and function, proteins have an extraordinarily diverse range of capabilities. In order to take advantage of their unparalleled specificity in the… (more)

Subjects/Keywords: Chemistry; Bioconjugation; Chemical Biology; Enzyme immobilization; Protein Chemistry; Protein Modification

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APA (6th Edition):

Palla, K. (2016). Development and Applications of N-terminal Protein Bioconjugation Reactions. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/5mv8940t

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):

Palla, Kanwal. “Development and Applications of N-terminal Protein Bioconjugation Reactions.” 2016. Thesis, University of California – Berkeley. Accessed June 19, 2019. http://www.escholarship.org/uc/item/5mv8940t.

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

MLA Handbook (7th Edition):

Palla, Kanwal. “Development and Applications of N-terminal Protein Bioconjugation Reactions.” 2016. Web. 19 Jun 2019.

Vancouver:

Palla K. Development and Applications of N-terminal Protein Bioconjugation Reactions. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2019 Jun 19]. Available from: http://www.escholarship.org/uc/item/5mv8940t.

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

Council of Science Editors:

Palla K. Development and Applications of N-terminal Protein Bioconjugation Reactions. [Thesis]. University of California – Berkeley; 2016. Available from: http://www.escholarship.org/uc/item/5mv8940t

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

16. Flanagan, Sean E. Hetero-Protein Coacervation and Complex Equilibria Between β-lactoglobulin and Lactoferrin.

Degree: MS(M.S.), Chemistry, 2014, U of Massachusetts : Masters

  Coacervation between the milk proteins β-lactoglobulin (BLG) and Lactoferrin (LF) was studied as a model system for hetero-protein coacervation (HPC). Equilibria among BLG/LF complexes… (more)

Subjects/Keywords: Coacervation; Hetero-Protein Coacervation; Protein-Protein Interactions; Complex Equilibrium; Lactoferrin; β-lactoglobulin; Analytical Chemistry; Biochemistry; Food Chemistry; Physical Chemistry; Polymer Chemistry

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APA (6th Edition):

Flanagan, S. E. (2014). Hetero-Protein Coacervation and Complex Equilibria Between β-lactoglobulin and Lactoferrin. (Masters Thesis). U of Massachusetts : Masters. Retrieved from http://scholarworks.umass.edu/theses/1179

Chicago Manual of Style (16th Edition):

Flanagan, Sean E. “Hetero-Protein Coacervation and Complex Equilibria Between β-lactoglobulin and Lactoferrin.” 2014. Masters Thesis, U of Massachusetts : Masters. Accessed June 19, 2019. http://scholarworks.umass.edu/theses/1179.

MLA Handbook (7th Edition):

Flanagan, Sean E. “Hetero-Protein Coacervation and Complex Equilibria Between β-lactoglobulin and Lactoferrin.” 2014. Web. 19 Jun 2019.

Vancouver:

Flanagan SE. Hetero-Protein Coacervation and Complex Equilibria Between β-lactoglobulin and Lactoferrin. [Internet] [Masters thesis]. U of Massachusetts : Masters; 2014. [cited 2019 Jun 19]. Available from: http://scholarworks.umass.edu/theses/1179.

Council of Science Editors:

Flanagan SE. Hetero-Protein Coacervation and Complex Equilibria Between β-lactoglobulin and Lactoferrin. [Masters Thesis]. U of Massachusetts : Masters; 2014. Available from: http://scholarworks.umass.edu/theses/1179


University of Washington

17. Anderson, Jordan Micheal. Caps - Turns - Loops: Designing Better β-Hairpins.

Degree: PhD, 2017, University of Washington

 As protein engineering promises advances in almost every field of science and medicine, a greater understanding of the protein folding problem is necessary to make… (more)

Subjects/Keywords: NMR; Peptide; Protein Design; Protein Folding; β-Hairpin; β-Sheet; Chemistry; Biochemistry; Organic chemistry; Chemistry

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APA (6th Edition):

Anderson, J. M. (2017). Caps - Turns - Loops: Designing Better β-Hairpins. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/40518

Chicago Manual of Style (16th Edition):

Anderson, Jordan Micheal. “Caps - Turns - Loops: Designing Better β-Hairpins.” 2017. Doctoral Dissertation, University of Washington. Accessed June 19, 2019. http://hdl.handle.net/1773/40518.

MLA Handbook (7th Edition):

Anderson, Jordan Micheal. “Caps - Turns - Loops: Designing Better β-Hairpins.” 2017. Web. 19 Jun 2019.

Vancouver:

Anderson JM. Caps - Turns - Loops: Designing Better β-Hairpins. [Internet] [Doctoral dissertation]. University of Washington; 2017. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/1773/40518.

Council of Science Editors:

Anderson JM. Caps - Turns - Loops: Designing Better β-Hairpins. [Doctoral Dissertation]. University of Washington; 2017. Available from: http://hdl.handle.net/1773/40518


University of South Florida

18. Du Boulay, Courtney Jerome. Virtual Screening for Inhibitors of Anti-apoptotic Proteins: DCK, BCL-XL, MCL-1, MDMX, and MDM2.

Degree: 2013, University of South Florida

 ←Within this dissertation the topic of virtual screening is discussed with regard to three different cancer targets and also a brief introduction of the tools… (more)

Subjects/Keywords: Cancer; Computational Chemistry; Medicinal Chemistry; Medicine; Protein Protein Interaction; Virtual Screening; Chemistry

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APA (6th Edition):

Du Boulay, C. J. (2013). Virtual Screening for Inhibitors of Anti-apoptotic Proteins: DCK, BCL-XL, MCL-1, MDMX, and MDM2. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/4664

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):

Du Boulay, Courtney Jerome. “Virtual Screening for Inhibitors of Anti-apoptotic Proteins: DCK, BCL-XL, MCL-1, MDMX, and MDM2.” 2013. Thesis, University of South Florida. Accessed June 19, 2019. https://scholarcommons.usf.edu/etd/4664.

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

MLA Handbook (7th Edition):

Du Boulay, Courtney Jerome. “Virtual Screening for Inhibitors of Anti-apoptotic Proteins: DCK, BCL-XL, MCL-1, MDMX, and MDM2.” 2013. Web. 19 Jun 2019.

Vancouver:

Du Boulay CJ. Virtual Screening for Inhibitors of Anti-apoptotic Proteins: DCK, BCL-XL, MCL-1, MDMX, and MDM2. [Internet] [Thesis]. University of South Florida; 2013. [cited 2019 Jun 19]. Available from: https://scholarcommons.usf.edu/etd/4664.

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

Council of Science Editors:

Du Boulay CJ. Virtual Screening for Inhibitors of Anti-apoptotic Proteins: DCK, BCL-XL, MCL-1, MDMX, and MDM2. [Thesis]. University of South Florida; 2013. Available from: https://scholarcommons.usf.edu/etd/4664

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


University of Michigan

19. Abulwerdi, Fardokht Assadi. Structure-Based Design, Synthesis and Evaluation of Novel and Selective Small-Molecule Inhibitors of the Anti-Apoptotic Protein Mcl-1.

Degree: PhD, Medicinal Chemistry, 2014, University of Michigan

 The mitochondrial pathway to apoptosis is regulated through the protein-protein interactions of pro- and anti-apoptotic members of Bcl-2 family proteins. Overexpression of the anti-apoptotic members… (more)

Subjects/Keywords: Anti-apoptotic Mcl-1; Medicinal Chemistry; Protein-protein Interaction Inhibitor; Cancer; Protein NMR Spectroscopy; Structure-activity Relationship; Biological Chemistry; Chemistry; Science

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APA (6th Edition):

Abulwerdi, F. A. (2014). Structure-Based Design, Synthesis and Evaluation of Novel and Selective Small-Molecule Inhibitors of the Anti-Apoptotic Protein Mcl-1. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/107109

Chicago Manual of Style (16th Edition):

Abulwerdi, Fardokht Assadi. “Structure-Based Design, Synthesis and Evaluation of Novel and Selective Small-Molecule Inhibitors of the Anti-Apoptotic Protein Mcl-1.” 2014. Doctoral Dissertation, University of Michigan. Accessed June 19, 2019. http://hdl.handle.net/2027.42/107109.

MLA Handbook (7th Edition):

Abulwerdi, Fardokht Assadi. “Structure-Based Design, Synthesis and Evaluation of Novel and Selective Small-Molecule Inhibitors of the Anti-Apoptotic Protein Mcl-1.” 2014. Web. 19 Jun 2019.

Vancouver:

Abulwerdi FA. Structure-Based Design, Synthesis and Evaluation of Novel and Selective Small-Molecule Inhibitors of the Anti-Apoptotic Protein Mcl-1. [Internet] [Doctoral dissertation]. University of Michigan; 2014. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/2027.42/107109.

Council of Science Editors:

Abulwerdi FA. Structure-Based Design, Synthesis and Evaluation of Novel and Selective Small-Molecule Inhibitors of the Anti-Apoptotic Protein Mcl-1. [Doctoral Dissertation]. University of Michigan; 2014. Available from: http://hdl.handle.net/2027.42/107109


University of Cincinnati

20. Tonddast-Navaei, Sam, M.S. Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines.

Degree: PhD, Arts and Sciences: Chemistry, 2014, University of Cincinnati

 Proteins are large complex molecules that play important roles in cellular activities such as DNA replication, molecular transport, cell immunity, and regulatory activities. Based on… (more)

Subjects/Keywords: Physical Chemistry; Protein unfolding; Protein translocation; Protein degradation; ATPase; p97; Molecular Dynamics

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APA (6th Edition):

Tonddast-Navaei, Sam, M. S. (2014). Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384869946

Chicago Manual of Style (16th Edition):

Tonddast-Navaei, Sam, M S. “Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines.” 2014. Doctoral Dissertation, University of Cincinnati. Accessed June 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384869946.

MLA Handbook (7th Edition):

Tonddast-Navaei, Sam, M S. “Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines.” 2014. Web. 19 Jun 2019.

Vancouver:

Tonddast-Navaei, Sam MS. Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines. [Internet] [Doctoral dissertation]. University of Cincinnati; 2014. [cited 2019 Jun 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384869946.

Council of Science Editors:

Tonddast-Navaei, Sam MS. Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines. [Doctoral Dissertation]. University of Cincinnati; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384869946


Bowling Green State University

21. Wang, Zijian. Single-Molecule Spectroscopy And Imaging Studies Of Protein Folding-Unfolding Conformational Dynamics: The Multiple-State And Multiple-Channel Energy Landscape.

Degree: PhD, Photochemical Sciences, 2016, Bowling Green State University

Protein conformational dynamics often plays a critical role in protein functions. We have characterized the spontaneous folding-unfolding conformational fluctuation dynamics of calmodulin (CaM) at thermodynamic… (more)

Subjects/Keywords: Chemistry; Protein Folding; Single-Molecule Spectroscopy; Protein-Protein Interactions; Condensed Phase Dynamics

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APA (6th Edition):

Wang, Z. (2016). Single-Molecule Spectroscopy And Imaging Studies Of Protein Folding-Unfolding Conformational Dynamics: The Multiple-State And Multiple-Channel Energy Landscape. (Doctoral Dissertation). Bowling Green State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1459942296

Chicago Manual of Style (16th Edition):

Wang, Zijian. “Single-Molecule Spectroscopy And Imaging Studies Of Protein Folding-Unfolding Conformational Dynamics: The Multiple-State And Multiple-Channel Energy Landscape.” 2016. Doctoral Dissertation, Bowling Green State University. Accessed June 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1459942296.

MLA Handbook (7th Edition):

Wang, Zijian. “Single-Molecule Spectroscopy And Imaging Studies Of Protein Folding-Unfolding Conformational Dynamics: The Multiple-State And Multiple-Channel Energy Landscape.” 2016. Web. 19 Jun 2019.

Vancouver:

Wang Z. Single-Molecule Spectroscopy And Imaging Studies Of Protein Folding-Unfolding Conformational Dynamics: The Multiple-State And Multiple-Channel Energy Landscape. [Internet] [Doctoral dissertation]. Bowling Green State University; 2016. [cited 2019 Jun 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1459942296.

Council of Science Editors:

Wang Z. Single-Molecule Spectroscopy And Imaging Studies Of Protein Folding-Unfolding Conformational Dynamics: The Multiple-State And Multiple-Channel Energy Landscape. [Doctoral Dissertation]. Bowling Green State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1459942296


University of California – Irvine

22. Weisman, Adam. Engineering the Nanoparticle-Protein Interface.

Degree: Chemistry, 2016, University of California – Irvine

 Nanomaterials are finding widespread use in biomedical applications. In particular, the ability of nanoparticles to penetrate into every corner of physiological systems suggests that they… (more)

Subjects/Keywords: Chemistry; Biogeochemistry; Materials Science; Medical device; Nanoparticle; Polymer; Protein; Protein detection; Protein purification

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APA (6th Edition):

Weisman, A. (2016). Engineering the Nanoparticle-Protein Interface. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/3553d5s0

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):

Weisman, Adam. “Engineering the Nanoparticle-Protein Interface.” 2016. Thesis, University of California – Irvine. Accessed June 19, 2019. http://www.escholarship.org/uc/item/3553d5s0.

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

MLA Handbook (7th Edition):

Weisman, Adam. “Engineering the Nanoparticle-Protein Interface.” 2016. Web. 19 Jun 2019.

Vancouver:

Weisman A. Engineering the Nanoparticle-Protein Interface. [Internet] [Thesis]. University of California – Irvine; 2016. [cited 2019 Jun 19]. Available from: http://www.escholarship.org/uc/item/3553d5s0.

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

Council of Science Editors:

Weisman A. Engineering the Nanoparticle-Protein Interface. [Thesis]. University of California – Irvine; 2016. Available from: http://www.escholarship.org/uc/item/3553d5s0

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


University of California – San Diego

23. Xu, Zhenzhu. Protein Adsorption on Metal Oxide Nanoparticle Surfaces: Effects of Various Influences on Protein-Surface Interactions and Protein Structure.

Degree: Chemistry, 2018, University of California – San Diego

 With the development of nanoscience and nanotechnology, the biocompatibility of nanomaterials is becoming increasingly important. As one of the most prevalent nanomaterials, metal oxide nanoparticles… (more)

Subjects/Keywords: Chemistry; ATR-FTIR; nanoparticles; nanotechnology; protein adsorption; protein corona; protein-surface interactions

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APA (6th Edition):

Xu, Z. (2018). Protein Adsorption on Metal Oxide Nanoparticle Surfaces: Effects of Various Influences on Protein-Surface Interactions and Protein Structure. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/9425f20d

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):

Xu, Zhenzhu. “Protein Adsorption on Metal Oxide Nanoparticle Surfaces: Effects of Various Influences on Protein-Surface Interactions and Protein Structure.” 2018. Thesis, University of California – San Diego. Accessed June 19, 2019. http://www.escholarship.org/uc/item/9425f20d.

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

MLA Handbook (7th Edition):

Xu, Zhenzhu. “Protein Adsorption on Metal Oxide Nanoparticle Surfaces: Effects of Various Influences on Protein-Surface Interactions and Protein Structure.” 2018. Web. 19 Jun 2019.

Vancouver:

Xu Z. Protein Adsorption on Metal Oxide Nanoparticle Surfaces: Effects of Various Influences on Protein-Surface Interactions and Protein Structure. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2019 Jun 19]. Available from: http://www.escholarship.org/uc/item/9425f20d.

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

Council of Science Editors:

Xu Z. Protein Adsorption on Metal Oxide Nanoparticle Surfaces: Effects of Various Influences on Protein-Surface Interactions and Protein Structure. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/9425f20d

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


University of Illinois – Urbana-Champaign

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

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

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Desai, Janish. “Targeting isoprenoid and quinone biosynthesis for antimicrobial discovery.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed June 19, 2019. http://hdl.handle.net/2142/95269.

MLA Handbook (7th Edition):

Desai, Janish. “Targeting isoprenoid and quinone biosynthesis for antimicrobial discovery.” 2016. Web. 19 Jun 2019.

Vancouver:

Desai J. Targeting isoprenoid and quinone biosynthesis for antimicrobial discovery. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/2142/95269.

Council of Science Editors:

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


University of North Texas

25. Barker, Andrew L. Archaeological Proteomics: Method Development and Analysis of Protein-Ceramic Binding.

Degree: 2010, University of North Texas

 The analysis of protein residues recovered from archaeological artifacts provides a unique opportunity to reveal new information about past societies. However, many scientists are currently… (more)

Subjects/Keywords: Archaeological residues; protein-ceramic interaction; protein extraction; Ceramics.; Protein binding.; Proteomics.; Archaeological chemistry.; Archaeology  – Methodology.

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APA (6th Edition):

Barker, A. L. (2010). Archaeological Proteomics: Method Development and Analysis of Protein-Ceramic Binding. (Thesis). University of North Texas. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc28392/

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):

Barker, Andrew L. “Archaeological Proteomics: Method Development and Analysis of Protein-Ceramic Binding.” 2010. Thesis, University of North Texas. Accessed June 19, 2019. https://digital.library.unt.edu/ark:/67531/metadc28392/.

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

MLA Handbook (7th Edition):

Barker, Andrew L. “Archaeological Proteomics: Method Development and Analysis of Protein-Ceramic Binding.” 2010. Web. 19 Jun 2019.

Vancouver:

Barker AL. Archaeological Proteomics: Method Development and Analysis of Protein-Ceramic Binding. [Internet] [Thesis]. University of North Texas; 2010. [cited 2019 Jun 19]. Available from: https://digital.library.unt.edu/ark:/67531/metadc28392/.

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

Council of Science Editors:

Barker AL. Archaeological Proteomics: Method Development and Analysis of Protein-Ceramic Binding. [Thesis]. University of North Texas; 2010. Available from: https://digital.library.unt.edu/ark:/67531/metadc28392/

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


University of Minnesota

26. Knutson, Kristofer James. The thermodynamic basis for the binding of lipids to annexin a5.

Degree: 2009, University of Minnesota

University of Minesota M.S. thesis. December 2009. Major: Chemistry. Advisor: Prof. Anne Hinderliter. 1 computer file (PDF); vii, 41 pages.

Protein-membrane interactions are a vital… (more)

Subjects/Keywords: Protein-membrane; Thermodynamics; Membrane; Lipids; Chemistry; Cell

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APA (6th Edition):

Knutson, K. J. (2009). The thermodynamic basis for the binding of lipids to annexin a5. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/59906

Chicago Manual of Style (16th Edition):

Knutson, Kristofer James. “The thermodynamic basis for the binding of lipids to annexin a5.” 2009. Masters Thesis, University of Minnesota. Accessed June 19, 2019. http://purl.umn.edu/59906.

MLA Handbook (7th Edition):

Knutson, Kristofer James. “The thermodynamic basis for the binding of lipids to annexin a5.” 2009. Web. 19 Jun 2019.

Vancouver:

Knutson KJ. The thermodynamic basis for the binding of lipids to annexin a5. [Internet] [Masters thesis]. University of Minnesota; 2009. [cited 2019 Jun 19]. Available from: http://purl.umn.edu/59906.

Council of Science Editors:

Knutson KJ. The thermodynamic basis for the binding of lipids to annexin a5. [Masters Thesis]. University of Minnesota; 2009. Available from: http://purl.umn.edu/59906


University of Minnesota

27. Schenewerk, Audrey Rose. The incorporation of nitrosocyanin copper binding loop into azurin.

Degree: MS, Chemistry, 2010, University of Minnesota

University of Minnesota M.S. thesis. July 2010. Major: Chemistry. Advisor: Dr. Steven M. Berry. 1 computer file (PDF); v, 56 pages. Ill. (some col.)

Metalloprotein… (more)

Subjects/Keywords: Azurin; Copper; Protein; Metalloprotein design; Chemistry

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APA (6th Edition):

Schenewerk, A. R. (2010). The incorporation of nitrosocyanin copper binding loop into azurin. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/93640

Chicago Manual of Style (16th Edition):

Schenewerk, Audrey Rose. “The incorporation of nitrosocyanin copper binding loop into azurin.” 2010. Masters Thesis, University of Minnesota. Accessed June 19, 2019. http://purl.umn.edu/93640.

MLA Handbook (7th Edition):

Schenewerk, Audrey Rose. “The incorporation of nitrosocyanin copper binding loop into azurin.” 2010. Web. 19 Jun 2019.

Vancouver:

Schenewerk AR. The incorporation of nitrosocyanin copper binding loop into azurin. [Internet] [Masters thesis]. University of Minnesota; 2010. [cited 2019 Jun 19]. Available from: http://purl.umn.edu/93640.

Council of Science Editors:

Schenewerk AR. The incorporation of nitrosocyanin copper binding loop into azurin. [Masters Thesis]. University of Minnesota; 2010. Available from: http://purl.umn.edu/93640


University of Colorado

28. Drake, Matthew Robert. Using Chemical Synthesis to Investigate Protein Glycosylation: O-Mannosylation Site Specifically Modulates the Stability and Cellulose Binding Affinity of Family 1 Carbohydrate Binding Modules.

Degree: MS, Chemistry & Biochemistry, 2014, University of Colorado

  Lignocellulosic biomass is a massive, but largely unexploited potential source of biofuel. The underutilization of this resource stems largely from the fact that cellulose… (more)

Subjects/Keywords: Biofuel; Cellulase; Cellulose; Glycosylation; Protein; Synthesis; Chemistry

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APA (6th Edition):

Drake, M. R. (2014). Using Chemical Synthesis to Investigate Protein Glycosylation: O-Mannosylation Site Specifically Modulates the Stability and Cellulose Binding Affinity of Family 1 Carbohydrate Binding Modules. (Masters Thesis). University of Colorado. Retrieved from http://scholar.colorado.edu/chem_gradetds/3

Chicago Manual of Style (16th Edition):

Drake, Matthew Robert. “Using Chemical Synthesis to Investigate Protein Glycosylation: O-Mannosylation Site Specifically Modulates the Stability and Cellulose Binding Affinity of Family 1 Carbohydrate Binding Modules.” 2014. Masters Thesis, University of Colorado. Accessed June 19, 2019. http://scholar.colorado.edu/chem_gradetds/3.

MLA Handbook (7th Edition):

Drake, Matthew Robert. “Using Chemical Synthesis to Investigate Protein Glycosylation: O-Mannosylation Site Specifically Modulates the Stability and Cellulose Binding Affinity of Family 1 Carbohydrate Binding Modules.” 2014. Web. 19 Jun 2019.

Vancouver:

Drake MR. Using Chemical Synthesis to Investigate Protein Glycosylation: O-Mannosylation Site Specifically Modulates the Stability and Cellulose Binding Affinity of Family 1 Carbohydrate Binding Modules. [Internet] [Masters thesis]. University of Colorado; 2014. [cited 2019 Jun 19]. Available from: http://scholar.colorado.edu/chem_gradetds/3.

Council of Science Editors:

Drake MR. Using Chemical Synthesis to Investigate Protein Glycosylation: O-Mannosylation Site Specifically Modulates the Stability and Cellulose Binding Affinity of Family 1 Carbohydrate Binding Modules. [Masters Thesis]. University of Colorado; 2014. Available from: http://scholar.colorado.edu/chem_gradetds/3


University of Kansas

29. Lei, Ming. Using Lysine-Reactive Fluorescent Dye for Surface Characterization of a Monoclonal Antibody.

Degree: MA, Pharmaceutical Chemistry, 2014, University of Kansas

 The last decade has witnessed a rapid growth in the development of protein pharmaceuticals for diagnostic and therapeutic purposes. The biopharmaceutical industry increasingly demands thorough… (more)

Subjects/Keywords: Chemistry; Fluorescent; labeling; mass spectrometry; protein structure

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APA (6th Edition):

Lei, M. (2014). Using Lysine-Reactive Fluorescent Dye for Surface Characterization of a Monoclonal Antibody. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/21645

Chicago Manual of Style (16th Edition):

Lei, Ming. “Using Lysine-Reactive Fluorescent Dye for Surface Characterization of a Monoclonal Antibody.” 2014. Masters Thesis, University of Kansas. Accessed June 19, 2019. http://hdl.handle.net/1808/21645.

MLA Handbook (7th Edition):

Lei, Ming. “Using Lysine-Reactive Fluorescent Dye for Surface Characterization of a Monoclonal Antibody.” 2014. Web. 19 Jun 2019.

Vancouver:

Lei M. Using Lysine-Reactive Fluorescent Dye for Surface Characterization of a Monoclonal Antibody. [Internet] [Masters thesis]. University of Kansas; 2014. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/1808/21645.

Council of Science Editors:

Lei M. Using Lysine-Reactive Fluorescent Dye for Surface Characterization of a Monoclonal Antibody. [Masters Thesis]. University of Kansas; 2014. Available from: http://hdl.handle.net/1808/21645


Portland State University

30. Mbiya, Wilbes. Substituent Effects on Reactivity and Allergenicity of Benzoquinone.

Degree: PhD, Chemistry, 2013, Portland State University

  Benzoquinone (BQ) is an extremely potent electrophilic contact allergen that haptenates endogenous proteins through Michael addition (MA). It is also hypothesized that BQ may… (more)

Subjects/Keywords: Quinone  – Reactivity; Quinone  – Allergenicity; Protein binding; Chemistry

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

APA (6th Edition):

Mbiya, W. (2013). Substituent Effects on Reactivity and Allergenicity of Benzoquinone. (Doctoral Dissertation). Portland State University. Retrieved from https://pdxscholar.library.pdx.edu/open_access_etds/1406

Chicago Manual of Style (16th Edition):

Mbiya, Wilbes. “Substituent Effects on Reactivity and Allergenicity of Benzoquinone.” 2013. Doctoral Dissertation, Portland State University. Accessed June 19, 2019. https://pdxscholar.library.pdx.edu/open_access_etds/1406.

MLA Handbook (7th Edition):

Mbiya, Wilbes. “Substituent Effects on Reactivity and Allergenicity of Benzoquinone.” 2013. Web. 19 Jun 2019.

Vancouver:

Mbiya W. Substituent Effects on Reactivity and Allergenicity of Benzoquinone. [Internet] [Doctoral dissertation]. Portland State University; 2013. [cited 2019 Jun 19]. Available from: https://pdxscholar.library.pdx.edu/open_access_etds/1406.

Council of Science Editors:

Mbiya W. Substituent Effects on Reactivity and Allergenicity of Benzoquinone. [Doctoral Dissertation]. Portland State University; 2013. Available from: https://pdxscholar.library.pdx.edu/open_access_etds/1406

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