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You searched for subject:(Protein chemistry). Showing records 1 – 30 of 1273 total matches.

[1] [2] [3] [4] [5] … [43]

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Freie Universität Berlin

1. Artner, Lukas M. Konvergente Synthesen multivalent bindender Glykokonjugate.

Degree: 2015, Freie Universität Berlin

 Die Bindungsereignisse von Glykoproteinen werden oft durch Lektine vermittelt und sind typischerweise kooperativ oder multivalent. In dieser Doktorarbeit wurden unterschiedliche Strategien angewandt um diese multivalenten… (more)

Subjects/Keywords: chemical biology; chemistry; multivalency; protein chemistry; 500 Naturwissenschaften und Mathematik::540 Chemie::547 Organische Chemie

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

APA (6th Edition):

Artner, L. M. (2015). Konvergente Synthesen multivalent bindender Glykokonjugate. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-13162

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):

Artner, Lukas M. “Konvergente Synthesen multivalent bindender Glykokonjugate.” 2015. Thesis, Freie Universität Berlin. Accessed February 28, 2020. http://dx.doi.org/10.17169/refubium-13162.

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

MLA Handbook (7th Edition):

Artner, Lukas M. “Konvergente Synthesen multivalent bindender Glykokonjugate.” 2015. Web. 28 Feb 2020.

Vancouver:

Artner LM. Konvergente Synthesen multivalent bindender Glykokonjugate. [Internet] [Thesis]. Freie Universität Berlin; 2015. [cited 2020 Feb 28]. Available from: http://dx.doi.org/10.17169/refubium-13162.

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

Council of Science Editors:

Artner LM. Konvergente Synthesen multivalent bindender Glykokonjugate. [Thesis]. Freie Universität Berlin; 2015. Available from: http://dx.doi.org/10.17169/refubium-13162

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


University of California – San Diego

2. 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 (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 February 28, 2020. 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. 28 Feb 2020.

Vancouver:

Kozachenko IA. Studies of Membrane Protein Folding by Bimolecular Fluorescence Quenching. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2020 Feb 28]. 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

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 February 28, 2020. 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. 28 Feb 2020.

Vancouver:

Bryan T. Criteria for Evolution of Successful Proteins: Fold Fitness and Domain Dynamics Explored. [Internet] [Doctoral dissertation]. University of New Mexico; 2014. [cited 2020 Feb 28]. 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

4. 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 February 28, 2020. 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. 28 Feb 2020.

Vancouver:

Richter A. Synthese niedermolekularer Verbindungen zur Stabilisierung von Protein-Protein-Interaktionen. [Internet] [Thesis]. Technische Universität Dortmund; 2011. [cited 2020 Feb 28]. 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


Freie Universität Berlin

5. Ye, Shijie. Ortsspezifischer Einbau der fluorierten Aminosäuren in einen pankreatischen Trypsin-Inhibitor.

Degree: 2014, Freie Universität Berlin

 Aufgrund seiner einzigartigen Eigenschaften erweist sich Fluor als ein vielfältiges Werkzeug in der pharmazeutischen Chemie und in den Materialwissenschaften. Der Einbau der C-F Bindung in… (more)

Subjects/Keywords: Fluorinated amino acids; BPTI; protein-protein interactions; protein crystallography; 500 Naturwissenschaften und Mathematik::540 Chemie

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APA (6th Edition):

Ye, S. (2014). Ortsspezifischer Einbau der fluorierten Aminosäuren in einen pankreatischen Trypsin-Inhibitor. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/13281

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):

Ye, Shijie. “Ortsspezifischer Einbau der fluorierten Aminosäuren in einen pankreatischen Trypsin-Inhibitor.” 2014. Thesis, Freie Universität Berlin. Accessed February 28, 2020. https://refubium.fu-berlin.de/handle/fub188/13281.

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

MLA Handbook (7th Edition):

Ye, Shijie. “Ortsspezifischer Einbau der fluorierten Aminosäuren in einen pankreatischen Trypsin-Inhibitor.” 2014. Web. 28 Feb 2020.

Vancouver:

Ye S. Ortsspezifischer Einbau der fluorierten Aminosäuren in einen pankreatischen Trypsin-Inhibitor. [Internet] [Thesis]. Freie Universität Berlin; 2014. [cited 2020 Feb 28]. Available from: https://refubium.fu-berlin.de/handle/fub188/13281.

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

Council of Science Editors:

Ye S. Ortsspezifischer Einbau der fluorierten Aminosäuren in einen pankreatischen Trypsin-Inhibitor. [Thesis]. Freie Universität Berlin; 2014. Available from: https://refubium.fu-berlin.de/handle/fub188/13281

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


University of New Mexico

6. 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 February 28, 2020. 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. 28 Feb 2020.

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 2020 Feb 28]. 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

7. 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 February 28, 2020. http://hdl.handle.net/10150/605218.

MLA Handbook (7th Edition):

Kumirov, Vlad K. “Mechanisms and Consequences of Evolving a New Protein Fold .” 2016. Web. 28 Feb 2020.

Vancouver:

Kumirov VK. Mechanisms and Consequences of Evolving a New Protein Fold . [Internet] [Doctoral dissertation]. University of Arizona; 2016. [cited 2020 Feb 28]. 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

8. 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 February 28, 2020. 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. 28 Feb 2020.

Vancouver:

Park MS. Computational Studies of Proteins: Dynamics and Interactions with Small Molecules. [Internet] [Doctoral dissertation]. University of Rochester; 2011. [cited 2020 Feb 28]. 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

9. 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 February 28, 2020. 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. 28 Feb 2020.

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 2020 Feb 28]. 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


Freie Universität Berlin

10. Mühlberg, Michaela. Chemoselektive Modifikationsstrategien für Peptide und Proteine im wässrigen Medium.

Degree: 2015, Freie Universität Berlin

 In dieser Doktorarbeit haben wir uns mit verschiedenen Möglichkeiten der chemoselektiven Funktionalisierung von Peptiden und Proteinen beschäftigt. Dabei wurden vier verschieden wissenschaftliche Ansätze ausgewählt, die… (more)

Subjects/Keywords: chemoselective; bioorthogonal; protein; peptide; amide; 500 Naturwissenschaften und Mathematik::540 Chemie::547 Organische Chemie

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APA (6th Edition):

Mühlberg, M. (2015). Chemoselektive Modifikationsstrategien für Peptide und Proteine im wässrigen Medium. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/12893

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):

Mühlberg, Michaela. “Chemoselektive Modifikationsstrategien für Peptide und Proteine im wässrigen Medium.” 2015. Thesis, Freie Universität Berlin. Accessed February 28, 2020. https://refubium.fu-berlin.de/handle/fub188/12893.

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

MLA Handbook (7th Edition):

Mühlberg, Michaela. “Chemoselektive Modifikationsstrategien für Peptide und Proteine im wässrigen Medium.” 2015. Web. 28 Feb 2020.

Vancouver:

Mühlberg M. Chemoselektive Modifikationsstrategien für Peptide und Proteine im wässrigen Medium. [Internet] [Thesis]. Freie Universität Berlin; 2015. [cited 2020 Feb 28]. Available from: https://refubium.fu-berlin.de/handle/fub188/12893.

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

Council of Science Editors:

Mühlberg M. Chemoselektive Modifikationsstrategien für Peptide und Proteine im wässrigen Medium. [Thesis]. Freie Universität Berlin; 2015. Available from: https://refubium.fu-berlin.de/handle/fub188/12893

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


University of Michigan

11. 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 February 28, 2020. http://hdl.handle.net/2027.42/145943.

MLA Handbook (7th Edition):

Clark, Jordan. “Structural Investigation of Binding Events in Proteins.” 2018. Web. 28 Feb 2020.

Vancouver:

Clark J. Structural Investigation of Binding Events in Proteins. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2020 Feb 28]. 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

12. 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 February 28, 2020. 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. 28 Feb 2020.

Vancouver:

Luechapanichkul R. Determination of the Sequence Specificity and Protein Substrates of Protein Phosphatases. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2020 Feb 28]. 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


University of Michigan

13. 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 February 28, 2020. 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. 28 Feb 2020.

Vancouver:

Sciore A. A General, Symmetry-Based Approach for the Assembly of Proteins into Nanoscale Polyhedra. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2020 Feb 28]. 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


National University of Ireland – Galway

14. 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 February 28, 2020. 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. 28 Feb 2020.

Vancouver:

McGovern RE. Calixarene-mediated protein assembly . [Internet] [Thesis]. National University of Ireland – Galway; 2014. [cited 2020 Feb 28]. 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


Michigan State University

15. 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 February 28, 2020. 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. 28 Feb 2020.

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 2020 Feb 28]. 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

16. 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 February 28, 2020. 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. 28 Feb 2020.

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 2020 Feb 28]. 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 Oxford

17. 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 February 28, 2020. 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. 28 Feb 2020.

Vancouver:

Gunnoo SB. Site-specific chemical modification of antibodies for the modulation of function. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2020 Feb 28]. 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

18. 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 February 28, 2020. 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. 28 Feb 2020.

Vancouver:

Manuel GP. Development of Protein Microarray Fabrication Methods for Analysis by Surface Plasmon Resonance Imaging. [Internet] [Thesis]. University of California – Irvine; 2017. [cited 2020 Feb 28]. 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


Arizona State University

19. Zhu, Fanyi. Foundational Studies for Array-based Electrophoretic Exclusion of Proteins.

Degree: Chemistry, 2019, Arizona State University

 Disease prevention and personalized treatment will be impacted by the continued integration of protein biomarkers into medical practice. While there are already numerous biomarkers used… (more)

Subjects/Keywords: Chemistry; Analytical chemistry; Electrophoretic exclusion; Microfluidics; Protein

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APA (6th Edition):

Zhu, F. (2019). Foundational Studies for Array-based Electrophoretic Exclusion of Proteins. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/53824

Chicago Manual of Style (16th Edition):

Zhu, Fanyi. “Foundational Studies for Array-based Electrophoretic Exclusion of Proteins.” 2019. Doctoral Dissertation, Arizona State University. Accessed February 28, 2020. http://repository.asu.edu/items/53824.

MLA Handbook (7th Edition):

Zhu, Fanyi. “Foundational Studies for Array-based Electrophoretic Exclusion of Proteins.” 2019. Web. 28 Feb 2020.

Vancouver:

Zhu F. Foundational Studies for Array-based Electrophoretic Exclusion of Proteins. [Internet] [Doctoral dissertation]. Arizona State University; 2019. [cited 2020 Feb 28]. Available from: http://repository.asu.edu/items/53824.

Council of Science Editors:

Zhu F. Foundational Studies for Array-based Electrophoretic Exclusion of Proteins. [Doctoral Dissertation]. Arizona State University; 2019. Available from: http://repository.asu.edu/items/53824


University of California – San Diego

20. 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 February 28, 2020. 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. 28 Feb 2020.

Vancouver:

Maniaci BM. Design of Metal-Controlled Protein-Protein Interactions. [Internet] [Thesis]. University of California – San Diego; 2019. [cited 2020 Feb 28]. 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 Michigan

21. 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 February 28, 2020. 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. 28 Feb 2020.

Vancouver:

Govindarajoo B. Template Based Modeling and Structural Refinement of Protein-Protein Interactions. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2020 Feb 28]. 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 Oxford

22. Hall, Zoe Lauren. Protein complexes in the gas phase : structural insights from ion mobility-mass spectrometry and computational modelling.

Degree: PhD, 2013, University of Oxford

 Structure determination of macromolecular protein assemblies remains a challenge for well-established experimental methods. In this thesis, an emerging structural technique, ion mobility-mass spectrometry (IM-MS) is… (more)

Subjects/Keywords: 572.636; Biophysical chemistry; Protein chemistry; ion mobility; mass spectrometry; protein complexes

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APA (6th Edition):

Hall, Z. L. (2013). Protein complexes in the gas phase : structural insights from ion mobility-mass spectrometry and computational modelling. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:a958f616-e37f-42e2-bf57-a38d58388b0c ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581425

Chicago Manual of Style (16th Edition):

Hall, Zoe Lauren. “Protein complexes in the gas phase : structural insights from ion mobility-mass spectrometry and computational modelling.” 2013. Doctoral Dissertation, University of Oxford. Accessed February 28, 2020. http://ora.ox.ac.uk/objects/uuid:a958f616-e37f-42e2-bf57-a38d58388b0c ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581425.

MLA Handbook (7th Edition):

Hall, Zoe Lauren. “Protein complexes in the gas phase : structural insights from ion mobility-mass spectrometry and computational modelling.” 2013. Web. 28 Feb 2020.

Vancouver:

Hall ZL. Protein complexes in the gas phase : structural insights from ion mobility-mass spectrometry and computational modelling. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2020 Feb 28]. Available from: http://ora.ox.ac.uk/objects/uuid:a958f616-e37f-42e2-bf57-a38d58388b0c ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581425.

Council of Science Editors:

Hall ZL. Protein complexes in the gas phase : structural insights from ion mobility-mass spectrometry and computational modelling. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:a958f616-e37f-42e2-bf57-a38d58388b0c ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581425


University of California – Berkeley

23. 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 February 28, 2020. 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. 28 Feb 2020.

Vancouver:

Palla K. Development and Applications of N-terminal Protein Bioconjugation Reactions. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2020 Feb 28]. 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


University of Vienna

24. 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 February 28, 2020. 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. 28 Feb 2020.

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 2020 Feb 28]. 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

25. 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 February 28, 2020. 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. 28 Feb 2020.

Vancouver:

Flanagan SE. Hetero-Protein Coacervation and Complex Equilibria Between β-lactoglobulin and Lactoferrin. [Internet] [Masters thesis]. U of Massachusetts : Masters; 2014. [cited 2020 Feb 28]. 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 South Florida

26. 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 February 28, 2020. 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. 28 Feb 2020.

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 2020 Feb 28]. 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 Washington

27. 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 February 28, 2020. http://hdl.handle.net/1773/40518.

MLA Handbook (7th Edition):

Anderson, Jordan Micheal. “Caps - Turns - Loops: Designing Better β-Hairpins.” 2017. Web. 28 Feb 2020.

Vancouver:

Anderson JM. Caps - Turns - Loops: Designing Better β-Hairpins. [Internet] [Doctoral dissertation]. University of Washington; 2017. [cited 2020 Feb 28]. 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


Freie Universität Berlin

28. Igde, Sinaida. Beurteilung des Einflusses verschiedener struktureller Merkmale auf die multivalente Thermodynamik und Kinetik von Präzisionsglykomakromolekülen.

Degree: 2016, Freie Universität Berlin

 Die vorliegende Arbeit beschäftigte sich mit der Synthese einer Serie von Präzisionsglykomakromolekülen und der Analyse der Thermodynamik and Kinetik der multivalenten Wechselwirkungen mit dem Modellektin… (more)

Subjects/Keywords: multivalency; sugar-protein interactions; binding thermodynamics; binding kinetics; precision glycomacromolecules; 500 Naturwissenschaften und Mathematik::540 Chemie::540 Chemie und zugeordnete Wissenschaften

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

APA (6th Edition):

Igde, S. (2016). Beurteilung des Einflusses verschiedener struktureller Merkmale auf die multivalente Thermodynamik und Kinetik von Präzisionsglykomakromolekülen. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-11266

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):

Igde, Sinaida. “Beurteilung des Einflusses verschiedener struktureller Merkmale auf die multivalente Thermodynamik und Kinetik von Präzisionsglykomakromolekülen.” 2016. Thesis, Freie Universität Berlin. Accessed February 28, 2020. http://dx.doi.org/10.17169/refubium-11266.

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

MLA Handbook (7th Edition):

Igde, Sinaida. “Beurteilung des Einflusses verschiedener struktureller Merkmale auf die multivalente Thermodynamik und Kinetik von Präzisionsglykomakromolekülen.” 2016. Web. 28 Feb 2020.

Vancouver:

Igde S. Beurteilung des Einflusses verschiedener struktureller Merkmale auf die multivalente Thermodynamik und Kinetik von Präzisionsglykomakromolekülen. [Internet] [Thesis]. Freie Universität Berlin; 2016. [cited 2020 Feb 28]. Available from: http://dx.doi.org/10.17169/refubium-11266.

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

Council of Science Editors:

Igde S. Beurteilung des Einflusses verschiedener struktureller Merkmale auf die multivalente Thermodynamik und Kinetik von Präzisionsglykomakromolekülen. [Thesis]. Freie Universität Berlin; 2016. Available from: http://dx.doi.org/10.17169/refubium-11266

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


Freie Universität Berlin

29. Linden, Arne Helge. Dynamic-Nuclear-Polarization in Nuclear-Magnetic-Resonance-Spectroscopy of Proteins.

Degree: 2013, Freie Universität Berlin

 Structure determination of protein-complexes and membrane-proteins with nuclear magnetic resonance (NMR) is limited by the low sensitivity of this method. Dynamic nuclear polarization (DNP) can… (more)

Subjects/Keywords: nuclear magnetic resonance; dynamic nuclear polarization; protein structures; 500 Naturwissenschaften und Mathematik::540 Chemie::540 Chemie und zugeordnete Wissenschaften

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

APA (6th Edition):

Linden, A. H. (2013). Dynamic-Nuclear-Polarization in Nuclear-Magnetic-Resonance-Spectroscopy of Proteins. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-13392

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):

Linden, Arne Helge. “Dynamic-Nuclear-Polarization in Nuclear-Magnetic-Resonance-Spectroscopy of Proteins.” 2013. Thesis, Freie Universität Berlin. Accessed February 28, 2020. http://dx.doi.org/10.17169/refubium-13392.

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

MLA Handbook (7th Edition):

Linden, Arne Helge. “Dynamic-Nuclear-Polarization in Nuclear-Magnetic-Resonance-Spectroscopy of Proteins.” 2013. Web. 28 Feb 2020.

Vancouver:

Linden AH. Dynamic-Nuclear-Polarization in Nuclear-Magnetic-Resonance-Spectroscopy of Proteins. [Internet] [Thesis]. Freie Universität Berlin; 2013. [cited 2020 Feb 28]. Available from: http://dx.doi.org/10.17169/refubium-13392.

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

Council of Science Editors:

Linden AH. Dynamic-Nuclear-Polarization in Nuclear-Magnetic-Resonance-Spectroscopy of Proteins. [Thesis]. Freie Universität Berlin; 2013. Available from: http://dx.doi.org/10.17169/refubium-13392

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


Freie Universität Berlin

30. Michel, Dana. Synthese von homogenen N-glykosylierten und GPI-verankerten Peptiden für die Semisynthese des Prion Proteins.

Degree: 2018, Freie Universität Berlin

 Das Prion Protein (PrP) ist ein GPI-verankertes Glykoprotein, das für übertragbare schwammartige Hirnleiden (Transmissible Spongiforme Enzephalopathie [TSE]) verantwortlich ist. Die Pathologie der Prionerkrankung wird mit… (more)

Subjects/Keywords: PrP; prion protein; glycopeptides; NCL; 500 Naturwissenschaften und Mathematik::540 Chemie::540 Chemie und zugeordnete Wissenschaften

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

APA (6th Edition):

Michel, D. (2018). Synthese von homogenen N-glykosylierten und GPI-verankerten Peptiden für die Semisynthese des Prion Proteins. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/12790

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):

Michel, Dana. “Synthese von homogenen N-glykosylierten und GPI-verankerten Peptiden für die Semisynthese des Prion Proteins.” 2018. Thesis, Freie Universität Berlin. Accessed February 28, 2020. https://refubium.fu-berlin.de/handle/fub188/12790.

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

MLA Handbook (7th Edition):

Michel, Dana. “Synthese von homogenen N-glykosylierten und GPI-verankerten Peptiden für die Semisynthese des Prion Proteins.” 2018. Web. 28 Feb 2020.

Vancouver:

Michel D. Synthese von homogenen N-glykosylierten und GPI-verankerten Peptiden für die Semisynthese des Prion Proteins. [Internet] [Thesis]. Freie Universität Berlin; 2018. [cited 2020 Feb 28]. Available from: https://refubium.fu-berlin.de/handle/fub188/12790.

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

Council of Science Editors:

Michel D. Synthese von homogenen N-glykosylierten und GPI-verankerten Peptiden für die Semisynthese des Prion Proteins. [Thesis]. Freie Universität Berlin; 2018. Available from: https://refubium.fu-berlin.de/handle/fub188/12790

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

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