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You searched for subject:(protein engineering). Showing records 1 – 30 of 873 total matches.

[1] [2] [3] [4] [5] … [30]

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Rutgers University

1. Rubenstein, Aliza, 1990-. Large-scale protease multispecificity: structure-based prediction and fitness landscape analysis.

Degree: PhD, Quantitative Biomedicine, 2018, Rutgers University

Proteases are ubiquitous and significant to both normal cellular functioning and disease states. They are generally multispecific, cleaving a set of substrates without recognizing other… (more)

Subjects/Keywords: Protein engineering

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APA (6th Edition):

Rubenstein, Aliza, 1. (2018). Large-scale protease multispecificity: structure-based prediction and fitness landscape analysis. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/56112/

Chicago Manual of Style (16th Edition):

Rubenstein, Aliza, 1990-. “Large-scale protease multispecificity: structure-based prediction and fitness landscape analysis.” 2018. Doctoral Dissertation, Rutgers University. Accessed February 17, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/56112/.

MLA Handbook (7th Edition):

Rubenstein, Aliza, 1990-. “Large-scale protease multispecificity: structure-based prediction and fitness landscape analysis.” 2018. Web. 17 Feb 2020.

Vancouver:

Rubenstein, Aliza 1. Large-scale protease multispecificity: structure-based prediction and fitness landscape analysis. [Internet] [Doctoral dissertation]. Rutgers University; 2018. [cited 2020 Feb 17]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/56112/.

Council of Science Editors:

Rubenstein, Aliza 1. Large-scale protease multispecificity: structure-based prediction and fitness landscape analysis. [Doctoral Dissertation]. Rutgers University; 2018. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/56112/


University of Alberta

2. Alford, Spencer Caleb. Development of fluorogenic fluorescent protein heterodimers.

Degree: PhD, Department of Chemistry, 2012, University of Alberta

 Fluorescent proteins (FPs) are indispensible biochemical tools. The concerted efforts of protein engineers have produced FPs spanning the visible colour spectrum. This wide variety of… (more)

Subjects/Keywords: protein engineering; fluorescent protein; biosensor

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APA (6th Edition):

Alford, S. C. (2012). Development of fluorogenic fluorescent protein heterodimers. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/hh63sw19n

Chicago Manual of Style (16th Edition):

Alford, Spencer Caleb. “Development of fluorogenic fluorescent protein heterodimers.” 2012. Doctoral Dissertation, University of Alberta. Accessed February 17, 2020. https://era.library.ualberta.ca/files/hh63sw19n.

MLA Handbook (7th Edition):

Alford, Spencer Caleb. “Development of fluorogenic fluorescent protein heterodimers.” 2012. Web. 17 Feb 2020.

Vancouver:

Alford SC. Development of fluorogenic fluorescent protein heterodimers. [Internet] [Doctoral dissertation]. University of Alberta; 2012. [cited 2020 Feb 17]. Available from: https://era.library.ualberta.ca/files/hh63sw19n.

Council of Science Editors:

Alford SC. Development of fluorogenic fluorescent protein heterodimers. [Doctoral Dissertation]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/hh63sw19n


The Ohio State University

3. Lavinder, Jason James. Analyzing the Sequence-Stability Landscape of the Four-helix Bundle Protein Rop: Developing High-Throughput Approaches for Combinatorial Biophysics and Protein Engineering.

Degree: PhD, Ohio State Biochemistry Program, 2009, The Ohio State University

  The inability to accurately decipher the relationship between protein sequence and structural stability presents a major difficulty in predicting the effects of mutation on… (more)

Subjects/Keywords: Biochemistry; protein engineering; protein biophysics; protein stability

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APA (6th Edition):

Lavinder, J. J. (2009). Analyzing the Sequence-Stability Landscape of the Four-helix Bundle Protein Rop: Developing High-Throughput Approaches for Combinatorial Biophysics and Protein Engineering. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1245427976

Chicago Manual of Style (16th Edition):

Lavinder, Jason James. “Analyzing the Sequence-Stability Landscape of the Four-helix Bundle Protein Rop: Developing High-Throughput Approaches for Combinatorial Biophysics and Protein Engineering.” 2009. Doctoral Dissertation, The Ohio State University. Accessed February 17, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1245427976.

MLA Handbook (7th Edition):

Lavinder, Jason James. “Analyzing the Sequence-Stability Landscape of the Four-helix Bundle Protein Rop: Developing High-Throughput Approaches for Combinatorial Biophysics and Protein Engineering.” 2009. Web. 17 Feb 2020.

Vancouver:

Lavinder JJ. Analyzing the Sequence-Stability Landscape of the Four-helix Bundle Protein Rop: Developing High-Throughput Approaches for Combinatorial Biophysics and Protein Engineering. [Internet] [Doctoral dissertation]. The Ohio State University; 2009. [cited 2020 Feb 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1245427976.

Council of Science Editors:

Lavinder JJ. Analyzing the Sequence-Stability Landscape of the Four-helix Bundle Protein Rop: Developing High-Throughput Approaches for Combinatorial Biophysics and Protein Engineering. [Doctoral Dissertation]. The Ohio State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1245427976


Washington University in St. Louis

4. Borgo, Benjamin. Strategies for Computational Protein Design with Application to the Development of a Biomolecular Tool-kit for Single Molecule Protein Sequencing.

Degree: PhD, Biology and Biomedical Sciences: Computational and Systems Biology, 2014, Washington University in St. Louis

  One of the key properties of proteins is that they exhibit remarkable affinities and specificities for small-molecule and peptide binding partners. To improve the… (more)

Subjects/Keywords: Protein design; Protein engineering; Protein sequencing; Proteomics

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APA (6th Edition):

Borgo, B. (2014). Strategies for Computational Protein Design with Application to the Development of a Biomolecular Tool-kit for Single Molecule Protein Sequencing. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/etd/1221

Chicago Manual of Style (16th Edition):

Borgo, Benjamin. “Strategies for Computational Protein Design with Application to the Development of a Biomolecular Tool-kit for Single Molecule Protein Sequencing.” 2014. Doctoral Dissertation, Washington University in St. Louis. Accessed February 17, 2020. https://openscholarship.wustl.edu/etd/1221.

MLA Handbook (7th Edition):

Borgo, Benjamin. “Strategies for Computational Protein Design with Application to the Development of a Biomolecular Tool-kit for Single Molecule Protein Sequencing.” 2014. Web. 17 Feb 2020.

Vancouver:

Borgo B. Strategies for Computational Protein Design with Application to the Development of a Biomolecular Tool-kit for Single Molecule Protein Sequencing. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2014. [cited 2020 Feb 17]. Available from: https://openscholarship.wustl.edu/etd/1221.

Council of Science Editors:

Borgo B. Strategies for Computational Protein Design with Application to the Development of a Biomolecular Tool-kit for Single Molecule Protein Sequencing. [Doctoral Dissertation]. Washington University in St. Louis; 2014. Available from: https://openscholarship.wustl.edu/etd/1221


University of Manchester

5. Hulley, Martyn. Engineering of the PETNR active site to accommodate novel α/β substituted enone substrates.

Degree: 2010, University of Manchester

 Experiments facilitating the engineering of the PETNR active site to accommodate a range of non natural enone substrates with substituents localised on the α and… (more)

Subjects/Keywords: Biocatalysis; protein engineering

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APA (6th Edition):

Hulley, M. (2010). Engineering of the PETNR active site to accommodate novel α/β substituted enone substrates. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:96347

Chicago Manual of Style (16th Edition):

Hulley, Martyn. “Engineering of the PETNR active site to accommodate novel α/β substituted enone substrates.” 2010. Doctoral Dissertation, University of Manchester. Accessed February 17, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:96347.

MLA Handbook (7th Edition):

Hulley, Martyn. “Engineering of the PETNR active site to accommodate novel α/β substituted enone substrates.” 2010. Web. 17 Feb 2020.

Vancouver:

Hulley M. Engineering of the PETNR active site to accommodate novel α/β substituted enone substrates. [Internet] [Doctoral dissertation]. University of Manchester; 2010. [cited 2020 Feb 17]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:96347.

Council of Science Editors:

Hulley M. Engineering of the PETNR active site to accommodate novel α/β substituted enone substrates. [Doctoral Dissertation]. University of Manchester; 2010. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:96347


University of Manchester

6. Hugentobler, Katharina. Development of new biocatalytic routes to pharmaceutical intermediates: a case study on ticagrelor.

Degree: 2014, University of Manchester

The research carried out within this thesis was aimed at the development andimplementation of a biocatalytic route towards Ticagrelor, a platelet-aggregationinhibitor. A bio-retrosynthetic consideration of… (more)

Subjects/Keywords: biocatalysis; protein engineering

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APA (6th Edition):

Hugentobler, K. (2014). Development of new biocatalytic routes to pharmaceutical intermediates: a case study on ticagrelor. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:240647

Chicago Manual of Style (16th Edition):

Hugentobler, Katharina. “Development of new biocatalytic routes to pharmaceutical intermediates: a case study on ticagrelor.” 2014. Doctoral Dissertation, University of Manchester. Accessed February 17, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:240647.

MLA Handbook (7th Edition):

Hugentobler, Katharina. “Development of new biocatalytic routes to pharmaceutical intermediates: a case study on ticagrelor.” 2014. Web. 17 Feb 2020.

Vancouver:

Hugentobler K. Development of new biocatalytic routes to pharmaceutical intermediates: a case study on ticagrelor. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2020 Feb 17]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:240647.

Council of Science Editors:

Hugentobler K. Development of new biocatalytic routes to pharmaceutical intermediates: a case study on ticagrelor. [Doctoral Dissertation]. University of Manchester; 2014. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:240647


University of Delaware

7. O'Brien, Christopher J. Colloidal protein-protein interactions as a design target for aggregation resistance .

Degree: 2018, University of Delaware

 Proteins therapeutics have emerged as an important class of biological macromolecules with the potential to improve survival rates and quality of life of patients suffering… (more)

Subjects/Keywords: Biological sciences; Applied sciences; Protein aggregation; Protein engineering; Protein stability; Protein-protein interactions

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APA (6th Edition):

O'Brien, C. J. (2018). Colloidal protein-protein interactions as a design target for aggregation resistance . (Doctoral Dissertation). University of Delaware. Retrieved from http://udspace.udel.edu/handle/19716/23763

Chicago Manual of Style (16th Edition):

O'Brien, Christopher J. “Colloidal protein-protein interactions as a design target for aggregation resistance .” 2018. Doctoral Dissertation, University of Delaware. Accessed February 17, 2020. http://udspace.udel.edu/handle/19716/23763.

MLA Handbook (7th Edition):

O'Brien, Christopher J. “Colloidal protein-protein interactions as a design target for aggregation resistance .” 2018. Web. 17 Feb 2020.

Vancouver:

O'Brien CJ. Colloidal protein-protein interactions as a design target for aggregation resistance . [Internet] [Doctoral dissertation]. University of Delaware; 2018. [cited 2020 Feb 17]. Available from: http://udspace.udel.edu/handle/19716/23763.

Council of Science Editors:

O'Brien CJ. Colloidal protein-protein interactions as a design target for aggregation resistance . [Doctoral Dissertation]. University of Delaware; 2018. Available from: http://udspace.udel.edu/handle/19716/23763


Rice University

8. Pandey, Naresh. Characterizing the tolerance of near infrared fluorescent bacterial phytochromes to random backbone fission and circular permutation.

Degree: PhD, Natural Sciences, 2016, Rice University

Protein fission, fusion, and circular permutation have been used to convert green fluorescent protein (GFP) family members into biosensors that dynamically report on cellular processes,… (more)

Subjects/Keywords: near infrared fluorescent protein; circular permutation; knotted protein; protein engineering

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APA (6th Edition):

Pandey, N. (2016). Characterizing the tolerance of near infrared fluorescent bacterial phytochromes to random backbone fission and circular permutation. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/96201

Chicago Manual of Style (16th Edition):

Pandey, Naresh. “Characterizing the tolerance of near infrared fluorescent bacterial phytochromes to random backbone fission and circular permutation.” 2016. Doctoral Dissertation, Rice University. Accessed February 17, 2020. http://hdl.handle.net/1911/96201.

MLA Handbook (7th Edition):

Pandey, Naresh. “Characterizing the tolerance of near infrared fluorescent bacterial phytochromes to random backbone fission and circular permutation.” 2016. Web. 17 Feb 2020.

Vancouver:

Pandey N. Characterizing the tolerance of near infrared fluorescent bacterial phytochromes to random backbone fission and circular permutation. [Internet] [Doctoral dissertation]. Rice University; 2016. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/1911/96201.

Council of Science Editors:

Pandey N. Characterizing the tolerance of near infrared fluorescent bacterial phytochromes to random backbone fission and circular permutation. [Doctoral Dissertation]. Rice University; 2016. Available from: http://hdl.handle.net/1911/96201


The Ohio State University

9. Liu, Xinyan. Studies of the <i>Manduca sexta</i> cadherin-like receptor binding epitopes of <i>Bacillus thuringiensis</i> Cry1Aa toxin and protein engineering of mosquitocidal activity.

Degree: PhD, Ohio State Biochemistry Program, 2005, The Ohio State University

  <i>Bacillus thuringiensis</i>, an aerobic, gram-positive spore-forming bacterium commonly found in soil, produces parasporal crystal (Cry) proteins with insecticidal activity against a wide range of… (more)

Subjects/Keywords: protein-protein interaction; protein engineering

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APA (6th Edition):

Liu, X. (2005). Studies of the <i>Manduca sexta</i> cadherin-like receptor binding epitopes of <i>Bacillus thuringiensis</i> Cry1Aa toxin and protein engineering of mosquitocidal activity. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1117655918

Chicago Manual of Style (16th Edition):

Liu, Xinyan. “Studies of the <i>Manduca sexta</i> cadherin-like receptor binding epitopes of <i>Bacillus thuringiensis</i> Cry1Aa toxin and protein engineering of mosquitocidal activity.” 2005. Doctoral Dissertation, The Ohio State University. Accessed February 17, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1117655918.

MLA Handbook (7th Edition):

Liu, Xinyan. “Studies of the <i>Manduca sexta</i> cadherin-like receptor binding epitopes of <i>Bacillus thuringiensis</i> Cry1Aa toxin and protein engineering of mosquitocidal activity.” 2005. Web. 17 Feb 2020.

Vancouver:

Liu X. Studies of the <i>Manduca sexta</i> cadherin-like receptor binding epitopes of <i>Bacillus thuringiensis</i> Cry1Aa toxin and protein engineering of mosquitocidal activity. [Internet] [Doctoral dissertation]. The Ohio State University; 2005. [cited 2020 Feb 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1117655918.

Council of Science Editors:

Liu X. Studies of the <i>Manduca sexta</i> cadherin-like receptor binding epitopes of <i>Bacillus thuringiensis</i> Cry1Aa toxin and protein engineering of mosquitocidal activity. [Doctoral Dissertation]. The Ohio State University; 2005. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1117655918


Penn State University

10. Schweiker, Katrina Lynn. Computational Design and Experimental Characterization of Proteins with Increased Stability and Solubility.

Degree: PhD, Integrative Biosciences, 2009, Penn State University

 The ability to design proteins from first principles will provide an efficient way to develop stabilized proteins, which could have a profound impact on a… (more)

Subjects/Keywords: protein stability; protein engineering; computational design; protein folding

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APA (6th Edition):

Schweiker, K. L. (2009). Computational Design and Experimental Characterization of Proteins with Increased Stability and Solubility. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/9400

Chicago Manual of Style (16th Edition):

Schweiker, Katrina Lynn. “Computational Design and Experimental Characterization of Proteins with Increased Stability and Solubility.” 2009. Doctoral Dissertation, Penn State University. Accessed February 17, 2020. https://etda.libraries.psu.edu/catalog/9400.

MLA Handbook (7th Edition):

Schweiker, Katrina Lynn. “Computational Design and Experimental Characterization of Proteins with Increased Stability and Solubility.” 2009. Web. 17 Feb 2020.

Vancouver:

Schweiker KL. Computational Design and Experimental Characterization of Proteins with Increased Stability and Solubility. [Internet] [Doctoral dissertation]. Penn State University; 2009. [cited 2020 Feb 17]. Available from: https://etda.libraries.psu.edu/catalog/9400.

Council of Science Editors:

Schweiker KL. Computational Design and Experimental Characterization of Proteins with Increased Stability and Solubility. [Doctoral Dissertation]. Penn State University; 2009. Available from: https://etda.libraries.psu.edu/catalog/9400


University of Wollongong

11. Barrett, Jeffrey R. Pragmatic protein domain identification.

Degree: PhD, 2014, University of Wollongong

  Studying proteins is hard. Even in well studied model systems, some proteins are recalcitrant to production in useful amounts in soluble form. These proteins… (more)

Subjects/Keywords: proteins; protein structure; protein engineering; protein evolution; EzrA

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APA (6th Edition):

Barrett, J. R. (2014). Pragmatic protein domain identification. (Doctoral Dissertation). University of Wollongong. Retrieved from 0601 BIOCHEMISTRY AND CELL BIOLOGY, 0605 MICROBIOLOGY ; https://ro.uow.edu.au/theses/4141

Chicago Manual of Style (16th Edition):

Barrett, Jeffrey R. “Pragmatic protein domain identification.” 2014. Doctoral Dissertation, University of Wollongong. Accessed February 17, 2020. 0601 BIOCHEMISTRY AND CELL BIOLOGY, 0605 MICROBIOLOGY ; https://ro.uow.edu.au/theses/4141.

MLA Handbook (7th Edition):

Barrett, Jeffrey R. “Pragmatic protein domain identification.” 2014. Web. 17 Feb 2020.

Vancouver:

Barrett JR. Pragmatic protein domain identification. [Internet] [Doctoral dissertation]. University of Wollongong; 2014. [cited 2020 Feb 17]. Available from: 0601 BIOCHEMISTRY AND CELL BIOLOGY, 0605 MICROBIOLOGY ; https://ro.uow.edu.au/theses/4141.

Council of Science Editors:

Barrett JR. Pragmatic protein domain identification. [Doctoral Dissertation]. University of Wollongong; 2014. Available from: 0601 BIOCHEMISTRY AND CELL BIOLOGY, 0605 MICROBIOLOGY ; https://ro.uow.edu.au/theses/4141


University of California – San Diego

12. 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 17, 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. 17 Feb 2020.

Vancouver:

Maniaci BM. Design of Metal-Controlled Protein-Protein Interactions. [Internet] [Thesis]. University of California – San Diego; 2019. [cited 2020 Feb 17]. 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


Princeton University

13. Stevens, Adam Joseph. Discovery, Design, and Deployment of Enhanced Split Inteins .

Degree: PhD, 2018, Princeton University

Protein splicing is a post-translational autoprocessing event in which an intervening protein (intein) spontaneously cleaves itself from a precursor protein while simultaneously ligating the adjacent… (more)

Subjects/Keywords: intein splicing; protein design; protein engineering; protein semisynthesis

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APA (6th Edition):

Stevens, A. J. (2018). Discovery, Design, and Deployment of Enhanced Split Inteins . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01f1881p574

Chicago Manual of Style (16th Edition):

Stevens, Adam Joseph. “Discovery, Design, and Deployment of Enhanced Split Inteins .” 2018. Doctoral Dissertation, Princeton University. Accessed February 17, 2020. http://arks.princeton.edu/ark:/88435/dsp01f1881p574.

MLA Handbook (7th Edition):

Stevens, Adam Joseph. “Discovery, Design, and Deployment of Enhanced Split Inteins .” 2018. Web. 17 Feb 2020.

Vancouver:

Stevens AJ. Discovery, Design, and Deployment of Enhanced Split Inteins . [Internet] [Doctoral dissertation]. Princeton University; 2018. [cited 2020 Feb 17]. Available from: http://arks.princeton.edu/ark:/88435/dsp01f1881p574.

Council of Science Editors:

Stevens AJ. Discovery, Design, and Deployment of Enhanced Split Inteins . [Doctoral Dissertation]. Princeton University; 2018. Available from: http://arks.princeton.edu/ark:/88435/dsp01f1881p574


Columbia University

14. Bulutoglu, Beyza. Engineering Biomolecular Interfaces for Applications in Biotechnology.

Degree: 2017, Columbia University

Protein interactions occurring through biomolecular interfaces play an important role in the circle of life. These interactions are responsible for cellular function, including RNA transcription,… (more)

Subjects/Keywords: Biotechnology; Protein-protein interactions; Protein engineering; Enzymes; Peptides; Biomolecules; Chemical engineering; Biomedical engineering

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APA (6th Edition):

Bulutoglu, B. (2017). Engineering Biomolecular Interfaces for Applications in Biotechnology. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D80002NC

Chicago Manual of Style (16th Edition):

Bulutoglu, Beyza. “Engineering Biomolecular Interfaces for Applications in Biotechnology.” 2017. Doctoral Dissertation, Columbia University. Accessed February 17, 2020. https://doi.org/10.7916/D80002NC.

MLA Handbook (7th Edition):

Bulutoglu, Beyza. “Engineering Biomolecular Interfaces for Applications in Biotechnology.” 2017. Web. 17 Feb 2020.

Vancouver:

Bulutoglu B. Engineering Biomolecular Interfaces for Applications in Biotechnology. [Internet] [Doctoral dissertation]. Columbia University; 2017. [cited 2020 Feb 17]. Available from: https://doi.org/10.7916/D80002NC.

Council of Science Editors:

Bulutoglu B. Engineering Biomolecular Interfaces for Applications in Biotechnology. [Doctoral Dissertation]. Columbia University; 2017. Available from: https://doi.org/10.7916/D80002NC


University of Ottawa

15. Davey, James A. Multistate Computational Protein Design: Theories, Methods, and Applications .

Degree: 2016, University of Ottawa

 Traditional computational protein design (CPD) calculations model sequence perturbations and evaluate their stabilities using a single fixed protein backbone template in an approach referred to… (more)

Subjects/Keywords: computational protein design; multistate design; protein engineering; molecular modeling; substrate multispecificity; protein stability; protein dynamics

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APA (6th Edition):

Davey, J. A. (2016). Multistate Computational Protein Design: Theories, Methods, and Applications . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/35541

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):

Davey, James A. “Multistate Computational Protein Design: Theories, Methods, and Applications .” 2016. Thesis, University of Ottawa. Accessed February 17, 2020. http://hdl.handle.net/10393/35541.

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

MLA Handbook (7th Edition):

Davey, James A. “Multistate Computational Protein Design: Theories, Methods, and Applications .” 2016. Web. 17 Feb 2020.

Vancouver:

Davey JA. Multistate Computational Protein Design: Theories, Methods, and Applications . [Internet] [Thesis]. University of Ottawa; 2016. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/10393/35541.

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

Council of Science Editors:

Davey JA. Multistate Computational Protein Design: Theories, Methods, and Applications . [Thesis]. University of Ottawa; 2016. Available from: http://hdl.handle.net/10393/35541

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


University of Utah

16. Chen, Hsiao-Nung. Deconstruction and reconstruction of a protein capsid.

Degree: PhD, Chemistry, 2014, University of Utah

 The self-assembly of multiple protein subunits via noncovalent interactions provides a diverse collection of nanoarchitectures. Polyhedral capsids represent a particularly interesting type of structure in… (more)

Subjects/Keywords: Capsid; Protein engineering; Self-assembly

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

APA (6th Edition):

Chen, H. (2014). Deconstruction and reconstruction of a protein capsid. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3139/rec/613

Chicago Manual of Style (16th Edition):

Chen, Hsiao-Nung. “Deconstruction and reconstruction of a protein capsid.” 2014. Doctoral Dissertation, University of Utah. Accessed February 17, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3139/rec/613.

MLA Handbook (7th Edition):

Chen, Hsiao-Nung. “Deconstruction and reconstruction of a protein capsid.” 2014. Web. 17 Feb 2020.

Vancouver:

Chen H. Deconstruction and reconstruction of a protein capsid. [Internet] [Doctoral dissertation]. University of Utah; 2014. [cited 2020 Feb 17]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3139/rec/613.

Council of Science Editors:

Chen H. Deconstruction and reconstruction of a protein capsid. [Doctoral Dissertation]. University of Utah; 2014. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3139/rec/613


Texas A&M University

17. Lum, Karin Tien. Directed evolution of phosphotriesterase: towards the efficient detoxification of sarin and soman.

Degree: 2004, Texas A&M University

 Directed evolution studies were done with PTE for the enhancement of hydrolysis of both sarin and soman analogs. Particular attention was focused on the toxic… (more)

Subjects/Keywords: protein engineering

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APA (6th Edition):

Lum, K. T. (2004). Directed evolution of phosphotriesterase: towards the efficient detoxification of sarin and soman. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/149

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):

Lum, Karin Tien. “Directed evolution of phosphotriesterase: towards the efficient detoxification of sarin and soman.” 2004. Thesis, Texas A&M University. Accessed February 17, 2020. http://hdl.handle.net/1969.1/149.

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

MLA Handbook (7th Edition):

Lum, Karin Tien. “Directed evolution of phosphotriesterase: towards the efficient detoxification of sarin and soman.” 2004. Web. 17 Feb 2020.

Vancouver:

Lum KT. Directed evolution of phosphotriesterase: towards the efficient detoxification of sarin and soman. [Internet] [Thesis]. Texas A&M University; 2004. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/1969.1/149.

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

Council of Science Editors:

Lum KT. Directed evolution of phosphotriesterase: towards the efficient detoxification of sarin and soman. [Thesis]. Texas A&M University; 2004. Available from: http://hdl.handle.net/1969.1/149

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


University of Minnesota

18. Strange, Jacob. Rational improvement of the activity of a nitrite reductase model.

Degree: MS, Chemistry, 2014, University of Minnesota

 Nitrite reductase (NiR) is a bacterial enzyme that catalyzes the one electron reduction of nitrite (NO2-) to nitric oxide (NO). Through site-directed PCR mutagenesis, variants… (more)

Subjects/Keywords: Azurin; Nitrite Reductase; Protein Engineering

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APA (6th Edition):

Strange, J. (2014). Rational improvement of the activity of a nitrite reductase model. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/165590

Chicago Manual of Style (16th Edition):

Strange, Jacob. “Rational improvement of the activity of a nitrite reductase model.” 2014. Masters Thesis, University of Minnesota. Accessed February 17, 2020. http://hdl.handle.net/11299/165590.

MLA Handbook (7th Edition):

Strange, Jacob. “Rational improvement of the activity of a nitrite reductase model.” 2014. Web. 17 Feb 2020.

Vancouver:

Strange J. Rational improvement of the activity of a nitrite reductase model. [Internet] [Masters thesis]. University of Minnesota; 2014. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/11299/165590.

Council of Science Editors:

Strange J. Rational improvement of the activity of a nitrite reductase model. [Masters Thesis]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/165590


University of Manchester

19. Hulley, Martyn. Engineering of the PETNR active site to accommodate novel α/β substituted enone substrates.

Degree: PhD, 2010, University of Manchester

 Experiments facilitating the engineering of the PETNR active site to accommodate a range of non natural enone substrates with substituents localised on the α and… (more)

Subjects/Keywords: 572.8; Biocatalysis; protein engineering

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APA (6th Edition):

Hulley, M. (2010). Engineering of the PETNR active site to accommodate novel α/β substituted enone substrates. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/engineering-of-the-petnr-active-site-to-accommodate-novel-alpha-substituted-enone-substrates(31c4828a-4f90-495a-8ab5-afbcb0482baf).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.529217

Chicago Manual of Style (16th Edition):

Hulley, Martyn. “Engineering of the PETNR active site to accommodate novel α/β substituted enone substrates.” 2010. Doctoral Dissertation, University of Manchester. Accessed February 17, 2020. https://www.research.manchester.ac.uk/portal/en/theses/engineering-of-the-petnr-active-site-to-accommodate-novel-alpha-substituted-enone-substrates(31c4828a-4f90-495a-8ab5-afbcb0482baf).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.529217.

MLA Handbook (7th Edition):

Hulley, Martyn. “Engineering of the PETNR active site to accommodate novel α/β substituted enone substrates.” 2010. Web. 17 Feb 2020.

Vancouver:

Hulley M. Engineering of the PETNR active site to accommodate novel α/β substituted enone substrates. [Internet] [Doctoral dissertation]. University of Manchester; 2010. [cited 2020 Feb 17]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/engineering-of-the-petnr-active-site-to-accommodate-novel-alpha-substituted-enone-substrates(31c4828a-4f90-495a-8ab5-afbcb0482baf).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.529217.

Council of Science Editors:

Hulley M. Engineering of the PETNR active site to accommodate novel α/β substituted enone substrates. [Doctoral Dissertation]. University of Manchester; 2010. Available from: https://www.research.manchester.ac.uk/portal/en/theses/engineering-of-the-petnr-active-site-to-accommodate-novel-alpha-substituted-enone-substrates(31c4828a-4f90-495a-8ab5-afbcb0482baf).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.529217


The Ohio State University

20. Nauerth, Michelle Jon. Role of the Discoidin Domain receptor proteins in atherosclerosis: Interaction with lipids and collagen.

Degree: PhD, Biochemistry Program, Ohio State, 2011, The Ohio State University

  Discoidin domain receptors (DDR1 and DDR2) are unique tyrosine kinase receptors (RTKs) in that they bind to and become phosphorylated by collagens, particularly collagen… (more)

Subjects/Keywords: Biochemistry; Discoidin Domain; protein engineering

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

APA (6th Edition):

Nauerth, M. J. (2011). Role of the Discoidin Domain receptor proteins in atherosclerosis: Interaction with lipids and collagen. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1316545109

Chicago Manual of Style (16th Edition):

Nauerth, Michelle Jon. “Role of the Discoidin Domain receptor proteins in atherosclerosis: Interaction with lipids and collagen.” 2011. Doctoral Dissertation, The Ohio State University. Accessed February 17, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1316545109.

MLA Handbook (7th Edition):

Nauerth, Michelle Jon. “Role of the Discoidin Domain receptor proteins in atherosclerosis: Interaction with lipids and collagen.” 2011. Web. 17 Feb 2020.

Vancouver:

Nauerth MJ. Role of the Discoidin Domain receptor proteins in atherosclerosis: Interaction with lipids and collagen. [Internet] [Doctoral dissertation]. The Ohio State University; 2011. [cited 2020 Feb 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1316545109.

Council of Science Editors:

Nauerth MJ. Role of the Discoidin Domain receptor proteins in atherosclerosis: Interaction with lipids and collagen. [Doctoral Dissertation]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1316545109


University of Western Australia

21. Mohamad Razif, Muhammad Fazril. Engineering RNA-binding proteins.

Degree: PhD, 2012, University of Western Australia

RNA-protein interactions have key roles in the regulation of gene expression and are vital for many cellular processes and complex developmental programs in eukaryotes. Proteins… (more)

Subjects/Keywords: Protein engineering; RNA binding proteins

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APA (6th Edition):

Mohamad Razif, M. F. (2012). Engineering RNA-binding proteins. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=34900&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Mohamad Razif, Muhammad Fazril. “Engineering RNA-binding proteins.” 2012. Doctoral Dissertation, University of Western Australia. Accessed February 17, 2020. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=34900&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Mohamad Razif, Muhammad Fazril. “Engineering RNA-binding proteins.” 2012. Web. 17 Feb 2020.

Vancouver:

Mohamad Razif MF. Engineering RNA-binding proteins. [Internet] [Doctoral dissertation]. University of Western Australia; 2012. [cited 2020 Feb 17]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=34900&local_base=GEN01-INS01.

Council of Science Editors:

Mohamad Razif MF. Engineering RNA-binding proteins. [Doctoral Dissertation]. University of Western Australia; 2012. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=34900&local_base=GEN01-INS01


Montana State University

22. Servid, Amy Eloise. Characterization and embellishment of protein cages for nanomedical and nanomaterial applications.

Degree: College of Letters & Science, 2014, Montana State University

 In nature, protein cages are found within the structures of viruses, heat shock proteins, and ferritins. They assemble from subunits into spherical oligomeric structures, which… (more)

Subjects/Keywords: Protein engineering.; Nanomedicine.; Lungs Immunology.

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APA (6th Edition):

Servid, A. E. (2014). Characterization and embellishment of protein cages for nanomedical and nanomaterial applications. (Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/9137

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):

Servid, Amy Eloise. “Characterization and embellishment of protein cages for nanomedical and nanomaterial applications.” 2014. Thesis, Montana State University. Accessed February 17, 2020. https://scholarworks.montana.edu/xmlui/handle/1/9137.

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

MLA Handbook (7th Edition):

Servid, Amy Eloise. “Characterization and embellishment of protein cages for nanomedical and nanomaterial applications.” 2014. Web. 17 Feb 2020.

Vancouver:

Servid AE. Characterization and embellishment of protein cages for nanomedical and nanomaterial applications. [Internet] [Thesis]. Montana State University; 2014. [cited 2020 Feb 17]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/9137.

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

Council of Science Editors:

Servid AE. Characterization and embellishment of protein cages for nanomedical and nanomaterial applications. [Thesis]. Montana State University; 2014. Available from: https://scholarworks.montana.edu/xmlui/handle/1/9137

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


Cornell University

23. Mansell, Thomas. A Suite Of Tools For Reporting And Engineering Protein Folding, Interactions, And Post-Translational Modifications In The Bacterial Periplasm .

Degree: 2012, Cornell University

 Therapeutic protein drugs are part of an emerging new generation of pharmaceutical products. However, production of such drugs is expensive due to the complex nature… (more)

Subjects/Keywords: Protein Engineering; Bacteria; Glycosylation

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APA (6th Edition):

Mansell, T. (2012). A Suite Of Tools For Reporting And Engineering Protein Folding, Interactions, And Post-Translational Modifications In The Bacterial Periplasm . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/29502

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):

Mansell, Thomas. “A Suite Of Tools For Reporting And Engineering Protein Folding, Interactions, And Post-Translational Modifications In The Bacterial Periplasm .” 2012. Thesis, Cornell University. Accessed February 17, 2020. http://hdl.handle.net/1813/29502.

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

MLA Handbook (7th Edition):

Mansell, Thomas. “A Suite Of Tools For Reporting And Engineering Protein Folding, Interactions, And Post-Translational Modifications In The Bacterial Periplasm .” 2012. Web. 17 Feb 2020.

Vancouver:

Mansell T. A Suite Of Tools For Reporting And Engineering Protein Folding, Interactions, And Post-Translational Modifications In The Bacterial Periplasm . [Internet] [Thesis]. Cornell University; 2012. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/1813/29502.

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

Council of Science Editors:

Mansell T. A Suite Of Tools For Reporting And Engineering Protein Folding, Interactions, And Post-Translational Modifications In The Bacterial Periplasm . [Thesis]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/29502

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


University of Colorado

24. Cordes, Amanda. Complex Stability Behavior in Novel Protein Constructs: Aggregation of Fc- and HSA- Based Fusion Proteins.

Degree: PhD, Chemical & Biochemical Engineering, 2011, University of Colorado

  The development of protein based biopharmaceuticals has resulted in the ability to treat many serious conditions, including endogenous protein deficiencies, cancer and autoimmune disorders.… (more)

Subjects/Keywords: Aggregation; Formulation; Protein; Chemical Engineering

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APA (6th Edition):

Cordes, A. (2011). Complex Stability Behavior in Novel Protein Constructs: Aggregation of Fc- and HSA- Based Fusion Proteins. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/20

Chicago Manual of Style (16th Edition):

Cordes, Amanda. “Complex Stability Behavior in Novel Protein Constructs: Aggregation of Fc- and HSA- Based Fusion Proteins.” 2011. Doctoral Dissertation, University of Colorado. Accessed February 17, 2020. https://scholar.colorado.edu/chbe_gradetds/20.

MLA Handbook (7th Edition):

Cordes, Amanda. “Complex Stability Behavior in Novel Protein Constructs: Aggregation of Fc- and HSA- Based Fusion Proteins.” 2011. Web. 17 Feb 2020.

Vancouver:

Cordes A. Complex Stability Behavior in Novel Protein Constructs: Aggregation of Fc- and HSA- Based Fusion Proteins. [Internet] [Doctoral dissertation]. University of Colorado; 2011. [cited 2020 Feb 17]. Available from: https://scholar.colorado.edu/chbe_gradetds/20.

Council of Science Editors:

Cordes A. Complex Stability Behavior in Novel Protein Constructs: Aggregation of Fc- and HSA- Based Fusion Proteins. [Doctoral Dissertation]. University of Colorado; 2011. Available from: https://scholar.colorado.edu/chbe_gradetds/20


Cornell University

25. Lata, James. Engineering A Rapid Point-Of-Care Diagnostic Platform Utilizing Tethered Enzyme Technology For Time-Sensitive Pathologies .

Degree: 2015, Cornell University

 The primary advances in creating a point-of-care testing (PoCT) diagnostic platform involve miniaturizing assays based on recognition of biomarker antigens with antibodies. This approach has… (more)

Subjects/Keywords: Protein Engineering; Diagnostic; Enzyme Immobilization

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APA (6th Edition):

Lata, J. (2015). Engineering A Rapid Point-Of-Care Diagnostic Platform Utilizing Tethered Enzyme Technology For Time-Sensitive Pathologies . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/40952

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):

Lata, James. “Engineering A Rapid Point-Of-Care Diagnostic Platform Utilizing Tethered Enzyme Technology For Time-Sensitive Pathologies .” 2015. Thesis, Cornell University. Accessed February 17, 2020. http://hdl.handle.net/1813/40952.

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

MLA Handbook (7th Edition):

Lata, James. “Engineering A Rapid Point-Of-Care Diagnostic Platform Utilizing Tethered Enzyme Technology For Time-Sensitive Pathologies .” 2015. Web. 17 Feb 2020.

Vancouver:

Lata J. Engineering A Rapid Point-Of-Care Diagnostic Platform Utilizing Tethered Enzyme Technology For Time-Sensitive Pathologies . [Internet] [Thesis]. Cornell University; 2015. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/1813/40952.

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

Council of Science Editors:

Lata J. Engineering A Rapid Point-Of-Care Diagnostic Platform Utilizing Tethered Enzyme Technology For Time-Sensitive Pathologies . [Thesis]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/40952

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


Colorado State University

26. Bjerke, Jennifer. Exploration of Protein Engineering Methods Towards Biomaterials, Therapeutic Protein Scaffolds, and Localization Detection within Mammalian Cells.

Degree: PhD, Chemistry, 2020, Colorado State University

 Proteins are large biomolecules entangled with complex chemistry that uniquely control the processes, function and efficiency of everyday life. These macromolecules are the final product… (more)

Subjects/Keywords: Nanobody; Chemical Biology; Protein Engineering

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APA (6th Edition):

Bjerke, J. (2020). Exploration of Protein Engineering Methods Towards Biomaterials, Therapeutic Protein Scaffolds, and Localization Detection within Mammalian Cells. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/199850

Chicago Manual of Style (16th Edition):

Bjerke, Jennifer. “Exploration of Protein Engineering Methods Towards Biomaterials, Therapeutic Protein Scaffolds, and Localization Detection within Mammalian Cells.” 2020. Doctoral Dissertation, Colorado State University. Accessed February 17, 2020. http://hdl.handle.net/10217/199850.

MLA Handbook (7th Edition):

Bjerke, Jennifer. “Exploration of Protein Engineering Methods Towards Biomaterials, Therapeutic Protein Scaffolds, and Localization Detection within Mammalian Cells.” 2020. Web. 17 Feb 2020.

Vancouver:

Bjerke J. Exploration of Protein Engineering Methods Towards Biomaterials, Therapeutic Protein Scaffolds, and Localization Detection within Mammalian Cells. [Internet] [Doctoral dissertation]. Colorado State University; 2020. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/10217/199850.

Council of Science Editors:

Bjerke J. Exploration of Protein Engineering Methods Towards Biomaterials, Therapeutic Protein Scaffolds, and Localization Detection within Mammalian Cells. [Doctoral Dissertation]. Colorado State University; 2020. Available from: http://hdl.handle.net/10217/199850


Rutgers University

27. Blacklock, Kristin, 1991-. New tools and approaches for computational protein design.

Degree: PhD, Quantitative Biomedicine, 2019, Rutgers University

This dissertation describes the development, benchmarking, validation, and application of computational methods, mostly written within the Rosetta suite of macromolecular modeling software, for the design… (more)

Subjects/Keywords: Protein engineering; Computational biology

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APA (6th Edition):

Blacklock, Kristin, 1. (2019). New tools and approaches for computational protein design. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/60017/

Chicago Manual of Style (16th Edition):

Blacklock, Kristin, 1991-. “New tools and approaches for computational protein design.” 2019. Doctoral Dissertation, Rutgers University. Accessed February 17, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/60017/.

MLA Handbook (7th Edition):

Blacklock, Kristin, 1991-. “New tools and approaches for computational protein design.” 2019. Web. 17 Feb 2020.

Vancouver:

Blacklock, Kristin 1. New tools and approaches for computational protein design. [Internet] [Doctoral dissertation]. Rutgers University; 2019. [cited 2020 Feb 17]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/60017/.

Council of Science Editors:

Blacklock, Kristin 1. New tools and approaches for computational protein design. [Doctoral Dissertation]. Rutgers University; 2019. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/60017/


Rutgers University

28. Hernandez, Nancy, 1991-. Towards overcoming the deficiencies of recently evolved biodegradative enzymes.

Degree: PhD, Chemistry and Chemical Biology, 2019, Rutgers University

This thesis describes a computational protein engineering approach, which utilizes protein assemblies and enzyme engineering, for the biodegradation of an endocrine disruptor and common pollutant,… (more)

Subjects/Keywords: Protein engineering; Atrazine  – Biodegradation

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APA (6th Edition):

Hernandez, Nancy, 1. (2019). Towards overcoming the deficiencies of recently evolved biodegradative enzymes. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/60164/

Chicago Manual of Style (16th Edition):

Hernandez, Nancy, 1991-. “Towards overcoming the deficiencies of recently evolved biodegradative enzymes.” 2019. Doctoral Dissertation, Rutgers University. Accessed February 17, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/60164/.

MLA Handbook (7th Edition):

Hernandez, Nancy, 1991-. “Towards overcoming the deficiencies of recently evolved biodegradative enzymes.” 2019. Web. 17 Feb 2020.

Vancouver:

Hernandez, Nancy 1. Towards overcoming the deficiencies of recently evolved biodegradative enzymes. [Internet] [Doctoral dissertation]. Rutgers University; 2019. [cited 2020 Feb 17]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/60164/.

Council of Science Editors:

Hernandez, Nancy 1. Towards overcoming the deficiencies of recently evolved biodegradative enzymes. [Doctoral Dissertation]. Rutgers University; 2019. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/60164/


University of Texas – Austin

29. Meyer, Adam Joshua. The evolution and engineering of T7 RNA polymerase.

Degree: PhD, Cell and Molecular Biology, 2014, University of Texas – Austin

 T7 RNA polymerase is a single protein capable of driving transcription from a simple promoter in virtually any context. This has made it a powerful… (more)

Subjects/Keywords: Molecular biology; Protein engineering

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APA (6th Edition):

Meyer, A. J. (2014). The evolution and engineering of T7 RNA polymerase. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/31292

Chicago Manual of Style (16th Edition):

Meyer, Adam Joshua. “The evolution and engineering of T7 RNA polymerase.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed February 17, 2020. http://hdl.handle.net/2152/31292.

MLA Handbook (7th Edition):

Meyer, Adam Joshua. “The evolution and engineering of T7 RNA polymerase.” 2014. Web. 17 Feb 2020.

Vancouver:

Meyer AJ. The evolution and engineering of T7 RNA polymerase. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/2152/31292.

Council of Science Editors:

Meyer AJ. The evolution and engineering of T7 RNA polymerase. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/31292


University of Manchester

30. Hugentobler, Katharina. Development of new biocatalytic routes to pharmaceutical intermediates : a case study on Ticagrelor.

Degree: PhD, 2014, University of Manchester

 The research carried out within this thesis was aimed at the development and implementation of a biocatalytic route towards Ticagrelor, a platelet-aggregation inhibitor. A bio-retrosynthetic… (more)

Subjects/Keywords: 660.6; biocatalysis; protein engineering

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APA (6th Edition):

Hugentobler, K. (2014). Development of new biocatalytic routes to pharmaceutical intermediates : a case study on Ticagrelor. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/development-of-new-biocatalytic-routes-to-pharmaceutical-intermediates-a-case-study-on-ticagrelor(0bda5532-3713-406b-873b-a40ee0d26a33).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.677730

Chicago Manual of Style (16th Edition):

Hugentobler, Katharina. “Development of new biocatalytic routes to pharmaceutical intermediates : a case study on Ticagrelor.” 2014. Doctoral Dissertation, University of Manchester. Accessed February 17, 2020. https://www.research.manchester.ac.uk/portal/en/theses/development-of-new-biocatalytic-routes-to-pharmaceutical-intermediates-a-case-study-on-ticagrelor(0bda5532-3713-406b-873b-a40ee0d26a33).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.677730.

MLA Handbook (7th Edition):

Hugentobler, Katharina. “Development of new biocatalytic routes to pharmaceutical intermediates : a case study on Ticagrelor.” 2014. Web. 17 Feb 2020.

Vancouver:

Hugentobler K. Development of new biocatalytic routes to pharmaceutical intermediates : a case study on Ticagrelor. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2020 Feb 17]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/development-of-new-biocatalytic-routes-to-pharmaceutical-intermediates-a-case-study-on-ticagrelor(0bda5532-3713-406b-873b-a40ee0d26a33).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.677730.

Council of Science Editors:

Hugentobler K. Development of new biocatalytic routes to pharmaceutical intermediates : a case study on Ticagrelor. [Doctoral Dissertation]. University of Manchester; 2014. Available from: https://www.research.manchester.ac.uk/portal/en/theses/development-of-new-biocatalytic-routes-to-pharmaceutical-intermediates-a-case-study-on-ticagrelor(0bda5532-3713-406b-873b-a40ee0d26a33).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.677730

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