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You searched for subject:(Protein chemistry). Showing records 1 – 30 of 1089 total matches.

[1] [2] [3] [4] [5] … [37]

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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 May 22, 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. 22 May 2019.

Vancouver:

Kozachenko IA. Studies of Membrane Protein Folding by Bimolecular Fluorescence Quenching. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2019 May 22]. 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

2. Richter, Anja. Synthese niedermolekularer Verbindungen zur Stabilisierung von Protein-Protein-Interaktionen.

Degree: 2011, Technische Universität Dortmund

 Die phytotoxische Wirkung des Naturstoffs Fusiocccin A, erstmals isoliert von Ballio et al. aus dem Pilz Fusicoccum amygadali, lässt sich auf die Stabilisierung der Interaktion… (more)

Subjects/Keywords: Fusicoccin; Organische Chemie; Protein-Protein-Interaktionen; Totalsynthese; 540; 570

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APA (6th Edition):

Richter, A. (2011). Synthese niedermolekularer Verbindungen zur Stabilisierung von Protein-Protein-Interaktionen. (Thesis). Technische Universität Dortmund. Retrieved from http://hdl.handle.net/2003/29051

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):

Richter, Anja. “Synthese niedermolekularer Verbindungen zur Stabilisierung von Protein-Protein-Interaktionen.” 2011. Thesis, Technische Universität Dortmund. Accessed May 22, 2019. http://hdl.handle.net/2003/29051.

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

MLA Handbook (7th Edition):

Richter, Anja. “Synthese niedermolekularer Verbindungen zur Stabilisierung von Protein-Protein-Interaktionen.” 2011. Web. 22 May 2019.

Vancouver:

Richter A. Synthese niedermolekularer Verbindungen zur Stabilisierung von Protein-Protein-Interaktionen. [Internet] [Thesis]. Technische Universität Dortmund; 2011. [cited 2019 May 22]. Available from: http://hdl.handle.net/2003/29051.

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

Council of Science Editors:

Richter A. Synthese niedermolekularer Verbindungen zur Stabilisierung von Protein-Protein-Interaktionen. [Thesis]. Technische Universität Dortmund; 2011. Available from: http://hdl.handle.net/2003/29051

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


University of New Mexico

3. 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 May 22, 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. 22 May 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 May 22]. 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

4. 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 May 22, 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. 22 May 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 May 22]. 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

5. Bestgen, Benoit. Selective modulation of the Protein Kinase CK2 : discovery, syntheses and characterization of non-ATP site inhibitors of CK2 : Modulation sélective de la Protéine Kinase CK2 : identification, synthèse et caractérisation d’inhibiteurs ne ciblant pas le site ATP.

Degree: Docteur es, Chimie thérapeutique, 2015, Université Claude Bernard – Lyon I

La Protéine Kinase CK2 est une enzyme tétramérique composé d'un dimère de sous-unité régulatrice (β) et de deux sous-unités catalytiques, CK2α et/ou CK2α'. La sous-unité… (more)

Subjects/Keywords: Oncologie; Chimie Médicinale; Biologie; Protéine Kinases; Oncology; Medicinal chemistry; Biology; Protein Kinase; Onkologie; Medizinische Chemie; Biologie; Protein Kinase; 540

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APA (6th Edition):

Bestgen, B. (2015). Selective modulation of the Protein Kinase CK2 : discovery, syntheses and characterization of non-ATP site inhibitors of CK2 : Modulation sélective de la Protéine Kinase CK2 : identification, synthèse et caractérisation d’inhibiteurs ne ciblant pas le site ATP. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2015LYO10247

Chicago Manual of Style (16th Edition):

Bestgen, Benoit. “Selective modulation of the Protein Kinase CK2 : discovery, syntheses and characterization of non-ATP site inhibitors of CK2 : Modulation sélective de la Protéine Kinase CK2 : identification, synthèse et caractérisation d’inhibiteurs ne ciblant pas le site ATP.” 2015. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed May 22, 2019. http://www.theses.fr/2015LYO10247.

MLA Handbook (7th Edition):

Bestgen, Benoit. “Selective modulation of the Protein Kinase CK2 : discovery, syntheses and characterization of non-ATP site inhibitors of CK2 : Modulation sélective de la Protéine Kinase CK2 : identification, synthèse et caractérisation d’inhibiteurs ne ciblant pas le site ATP.” 2015. Web. 22 May 2019.

Vancouver:

Bestgen B. Selective modulation of the Protein Kinase CK2 : discovery, syntheses and characterization of non-ATP site inhibitors of CK2 : Modulation sélective de la Protéine Kinase CK2 : identification, synthèse et caractérisation d’inhibiteurs ne ciblant pas le site ATP. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2015. [cited 2019 May 22]. Available from: http://www.theses.fr/2015LYO10247.

Council of Science Editors:

Bestgen B. Selective modulation of the Protein Kinase CK2 : discovery, syntheses and characterization of non-ATP site inhibitors of CK2 : Modulation sélective de la Protéine Kinase CK2 : identification, synthèse et caractérisation d’inhibiteurs ne ciblant pas le site ATP. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2015. Available from: http://www.theses.fr/2015LYO10247


University of Arizona

6. 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 May 22, 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. 22 May 2019.

Vancouver:

Kumirov VK. Mechanisms and Consequences of Evolving a New Protein Fold . [Internet] [Doctoral dissertation]. University of Arizona; 2016. [cited 2019 May 22]. 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

7. 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 May 22, 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. 22 May 2019.

Vancouver:

Park MS. Computational Studies of Proteins: Dynamics and Interactions with Small Molecules. [Internet] [Doctoral dissertation]. University of Rochester; 2011. [cited 2019 May 22]. 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

8. 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 May 22, 2019. http://hdl.handle.net/2027.42/145943.

MLA Handbook (7th Edition):

Clark, Jordan. “Structural Investigation of Binding Events in Proteins.” 2018. Web. 22 May 2019.

Vancouver:

Clark J. Structural Investigation of Binding Events in Proteins. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2019 May 22]. 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

9. 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 May 22, 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. 22 May 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 May 22]. 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


National University of Ireland – Galway

10. McGovern, Róise Ella. Calixarene-mediated protein assembly .

Degree: 2014, National University of Ireland – Galway

 Solved the first crystal structure of a protein-calixarene complex (at 1.4 Angstrom resolution). The results provide exact structural information on the amino acid preference of… (more)

Subjects/Keywords: Protein assembly; Calixarene; Chemistry

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APA (6th Edition):

McGovern, R. E. (2014). Calixarene-mediated protein assembly . (Thesis). National University of Ireland – Galway. Retrieved from http://hdl.handle.net/10379/4552

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):

McGovern, Róise Ella. “Calixarene-mediated protein assembly .” 2014. Thesis, National University of Ireland – Galway. Accessed May 22, 2019. http://hdl.handle.net/10379/4552.

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

MLA Handbook (7th Edition):

McGovern, Róise Ella. “Calixarene-mediated protein assembly .” 2014. Web. 22 May 2019.

Vancouver:

McGovern RE. Calixarene-mediated protein assembly . [Internet] [Thesis]. National University of Ireland – Galway; 2014. [cited 2019 May 22]. Available from: http://hdl.handle.net/10379/4552.

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

Council of Science Editors:

McGovern RE. Calixarene-mediated protein assembly . [Thesis]. National University of Ireland – Galway; 2014. Available from: http://hdl.handle.net/10379/4552

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


University of Michigan

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

Degree: PhD, Chemistry, 2016, University of Michigan

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Sciore, Aaron. “A General, Symmetry-Based Approach for the Assembly of Proteins into Nanoscale Polyhedra.” 2016. Doctoral Dissertation, University of Michigan. Accessed May 22, 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. 22 May 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 May 22]. 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

12. 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 May 22, 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. 22 May 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 May 22]. 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


Michigan State University

13. 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 May 22, 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. 22 May 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 May 22]. 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 Vienna

14. Weber, Christine. Investigations into the interaction between the beta-secretase protein BACE1 and a member of the reticulon family, RTN3.

Degree: 2010, University of Vienna

Mit steigender Prävalenz von Morbus Alzheimer in den Industrienationen wird auch die bisher erfolglose Suche nach einer effektiven Pharmakotherapie immer dringlicher. Gegenwärtig verfügbare Medikamente verbessern… (more)

Subjects/Keywords: 44.42 Pharmazeutische Chemie; Alzheimer / beta-Secretase Inhibitoren / Protein Interaktionen; Alzheimer's disease / beta-secretase inhibitors / protein-protein interactions

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APA (6th Edition):

Weber, C. (2010). Investigations into the interaction between the beta-secretase protein BACE1 and a member of the reticulon family, RTN3. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/8628/

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):

Weber, Christine. “Investigations into the interaction between the beta-secretase protein BACE1 and a member of the reticulon family, RTN3.” 2010. Thesis, University of Vienna. Accessed May 22, 2019. http://othes.univie.ac.at/8628/.

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

MLA Handbook (7th Edition):

Weber, Christine. “Investigations into the interaction between the beta-secretase protein BACE1 and a member of the reticulon family, RTN3.” 2010. Web. 22 May 2019.

Vancouver:

Weber C. Investigations into the interaction between the beta-secretase protein BACE1 and a member of the reticulon family, RTN3. [Internet] [Thesis]. University of Vienna; 2010. [cited 2019 May 22]. Available from: http://othes.univie.ac.at/8628/.

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

Council of Science Editors:

Weber C. Investigations into the interaction between the beta-secretase protein BACE1 and a member of the reticulon family, RTN3. [Thesis]. University of Vienna; 2010. Available from: http://othes.univie.ac.at/8628/

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


University of Oxford

15. Gunnoo, Smita Bye. Site-specific chemical modification of antibodies for the modulation of function.

Degree: PhD, 2013, University of Oxford

 Chemical modification of antibodies is critical for many research areas including therapeutic and biotechnological applications. In particular, strategies for site-specific chemical modification via non-natural amino… (more)

Subjects/Keywords: 547; Organic chemistry; Chemical Biology; Protein chemistry

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APA (6th Edition):

Gunnoo, S. B. (2013). Site-specific chemical modification of antibodies for the modulation of function. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:8857b207-c70d-4656-8279-9bcbfce2a8bd ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644879

Chicago Manual of Style (16th Edition):

Gunnoo, Smita Bye. “Site-specific chemical modification of antibodies for the modulation of function.” 2013. Doctoral Dissertation, University of Oxford. Accessed May 22, 2019. http://ora.ox.ac.uk/objects/uuid:8857b207-c70d-4656-8279-9bcbfce2a8bd ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644879.

MLA Handbook (7th Edition):

Gunnoo, Smita Bye. “Site-specific chemical modification of antibodies for the modulation of function.” 2013. Web. 22 May 2019.

Vancouver:

Gunnoo SB. Site-specific chemical modification of antibodies for the modulation of function. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2019 May 22]. Available from: http://ora.ox.ac.uk/objects/uuid:8857b207-c70d-4656-8279-9bcbfce2a8bd ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644879.

Council of Science Editors:

Gunnoo SB. Site-specific chemical modification of antibodies for the modulation of function. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:8857b207-c70d-4656-8279-9bcbfce2a8bd ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644879


University of California – Irvine

16. 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 May 22, 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. 22 May 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 May 22]. 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

17. 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 May 22, 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. 22 May 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 May 22]. 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

18. 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 May 22, 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. 22 May 2019.

Vancouver:

Govindarajoo B. Template Based Modeling and Structural Refinement of Protein-Protein Interactions. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2019 May 22]. 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 – Berkeley

19. 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 May 22, 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. 22 May 2019.

Vancouver:

Palla K. Development and Applications of N-terminal Protein Bioconjugation Reactions. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2019 May 22]. 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

20. 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 May 22, 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. 22 May 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 May 22]. 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

21. 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 May 22, 2019. http://hdl.handle.net/1773/40518.

MLA Handbook (7th Edition):

Anderson, Jordan Micheal. “Caps - Turns - Loops: Designing Better β-Hairpins.” 2017. Web. 22 May 2019.

Vancouver:

Anderson JM. Caps - Turns - Loops: Designing Better β-Hairpins. [Internet] [Doctoral dissertation]. University of Washington; 2017. [cited 2019 May 22]. 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

22. 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 May 22, 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. 22 May 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 May 22]. 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

23. 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 May 22, 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. 22 May 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 May 22]. 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


Louisiana State University

24. Thomasson, Margaret Sara. Investigating the Structure of the Papain-Inhibitor Complex using SPR and NMR.

Degree: PhD, Chemistry, 2016, Louisiana State University

 Cysteine proteases (CPs) are enzymes with a nucleophilic thiol in their active sites. Inhibitors of cysteine proteases (ICPs) occur naturally in bacterial pathogens and some… (more)

Subjects/Keywords: analytical chemistry; protein complexes; protein-protein interactions; NMR; SPR; papain; biochemistry; AFM; structure elucidation

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APA (6th Edition):

Thomasson, M. S. (2016). Investigating the Structure of the Papain-Inhibitor Complex using SPR and NMR. (Doctoral Dissertation). Louisiana State University. Retrieved from etd-07052016-085127 ; https://digitalcommons.lsu.edu/gradschool_dissertations/493

Chicago Manual of Style (16th Edition):

Thomasson, Margaret Sara. “Investigating the Structure of the Papain-Inhibitor Complex using SPR and NMR.” 2016. Doctoral Dissertation, Louisiana State University. Accessed May 22, 2019. etd-07052016-085127 ; https://digitalcommons.lsu.edu/gradschool_dissertations/493.

MLA Handbook (7th Edition):

Thomasson, Margaret Sara. “Investigating the Structure of the Papain-Inhibitor Complex using SPR and NMR.” 2016. Web. 22 May 2019.

Vancouver:

Thomasson MS. Investigating the Structure of the Papain-Inhibitor Complex using SPR and NMR. [Internet] [Doctoral dissertation]. Louisiana State University; 2016. [cited 2019 May 22]. Available from: etd-07052016-085127 ; https://digitalcommons.lsu.edu/gradschool_dissertations/493.

Council of Science Editors:

Thomasson MS. Investigating the Structure of the Papain-Inhibitor Complex using SPR and NMR. [Doctoral Dissertation]. Louisiana State University; 2016. Available from: etd-07052016-085127 ; https://digitalcommons.lsu.edu/gradschool_dissertations/493


University of Cincinnati

25. 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 May 22, 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. 22 May 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 May 22]. 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

26. 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 May 22, 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. 22 May 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 May 22]. 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

27. 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 May 22, 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. 22 May 2019.

Vancouver:

Weisman A. Engineering the Nanoparticle-Protein Interface. [Internet] [Thesis]. University of California – Irvine; 2016. [cited 2019 May 22]. 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 Nevada – Las Vegas

28. Ibarra, Rebeca Lea. The San1 Ubiquitin Ligase Functions Preferentially with Ubiquitin-Conjugating Enzyme Ubc1 During Protein Quality Control.

Degree: MS, Chemistry and Biochemistry, 2016, University of Nevada – Las Vegas

Protein quality control (PQC) is a critical process wherein misfolded or damaged proteins are cleared from the cell to maintain protein homeostasis. In eukaryotic… (more)

Subjects/Keywords: Protein Degradation; Protein Misfolding; Protein Quality Control; Ubiquitin; Ubiquitin-Conjugating Enzyme; Ubiquitin Ligase; Biochemistry; Chemistry

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APA (6th Edition):

Ibarra, R. L. (2016). The San1 Ubiquitin Ligase Functions Preferentially with Ubiquitin-Conjugating Enzyme Ubc1 During Protein Quality Control. (Masters Thesis). University of Nevada – Las Vegas. Retrieved from https://digitalscholarship.unlv.edu/thesesdissertations/2783

Chicago Manual of Style (16th Edition):

Ibarra, Rebeca Lea. “The San1 Ubiquitin Ligase Functions Preferentially with Ubiquitin-Conjugating Enzyme Ubc1 During Protein Quality Control.” 2016. Masters Thesis, University of Nevada – Las Vegas. Accessed May 22, 2019. https://digitalscholarship.unlv.edu/thesesdissertations/2783.

MLA Handbook (7th Edition):

Ibarra, Rebeca Lea. “The San1 Ubiquitin Ligase Functions Preferentially with Ubiquitin-Conjugating Enzyme Ubc1 During Protein Quality Control.” 2016. Web. 22 May 2019.

Vancouver:

Ibarra RL. The San1 Ubiquitin Ligase Functions Preferentially with Ubiquitin-Conjugating Enzyme Ubc1 During Protein Quality Control. [Internet] [Masters thesis]. University of Nevada – Las Vegas; 2016. [cited 2019 May 22]. Available from: https://digitalscholarship.unlv.edu/thesesdissertations/2783.

Council of Science Editors:

Ibarra RL. The San1 Ubiquitin Ligase Functions Preferentially with Ubiquitin-Conjugating Enzyme Ubc1 During Protein Quality Control. [Masters Thesis]. University of Nevada – Las Vegas; 2016. Available from: https://digitalscholarship.unlv.edu/thesesdissertations/2783


University of North Texas

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

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 May 22, 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. 22 May 2019.

Vancouver:

Barker AL. Archaeological Proteomics: Method Development and Analysis of Protein-Ceramic Binding. [Internet] [Thesis]. University of North Texas; 2010. [cited 2019 May 22]. 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 California – San Diego

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

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 May 22, 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. 22 May 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 May 22]. 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

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