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You searched for subject:(protein engineering). Showing records 1 – 30 of 1023 total matches.

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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 March 04, 2021. 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. 04 Mar 2021.

Vancouver:

Rubenstein, Aliza 1. Large-scale protease multispecificity: structure-based prediction and fitness landscape analysis. [Internet] [Doctoral dissertation]. Rutgers University; 2018. [cited 2021 Mar 04]. 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 March 04, 2021. https://era.library.ualberta.ca/files/hh63sw19n.

MLA Handbook (7th Edition):

Alford, Spencer Caleb. “Development of fluorogenic fluorescent protein heterodimers.” 2012. Web. 04 Mar 2021.

Vancouver:

Alford SC. Development of fluorogenic fluorescent protein heterodimers. [Internet] [Doctoral dissertation]. University of Alberta; 2012. [cited 2021 Mar 04]. 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


University of Ottawa

3. Eason, Matthew. A GFP-Based Sensor to Detect Transiently Expressed Proteins .

Degree: 2020, University of Ottawa

 Green fluorescent protein (GFP) fusion tags are commonly used to study protein expression and cellular localization in vivo. But, GFP must undergo an autogenic post-translational… (more)

Subjects/Keywords: Biosensor; Fluorescent Protein; Protein Engineering

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APA (6th Edition):

Eason, M. (2020). A GFP-Based Sensor to Detect Transiently Expressed Proteins . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/40500

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):

Eason, Matthew. “A GFP-Based Sensor to Detect Transiently Expressed Proteins .” 2020. Thesis, University of Ottawa. Accessed March 04, 2021. http://hdl.handle.net/10393/40500.

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

MLA Handbook (7th Edition):

Eason, Matthew. “A GFP-Based Sensor to Detect Transiently Expressed Proteins .” 2020. Web. 04 Mar 2021.

Vancouver:

Eason M. A GFP-Based Sensor to Detect Transiently Expressed Proteins . [Internet] [Thesis]. University of Ottawa; 2020. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/10393/40500.

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

Council of Science Editors:

Eason M. A GFP-Based Sensor to Detect Transiently Expressed Proteins . [Thesis]. University of Ottawa; 2020. Available from: http://hdl.handle.net/10393/40500

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


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 March 04, 2021. 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. 04 Mar 2021.

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 2021 Mar 04]. 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. 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 March 04, 2021. 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. 04 Mar 2021.

Vancouver:

Hugentobler K. Development of new biocatalytic routes to pharmaceutical intermediates: a case study on ticagrelor. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2021 Mar 04]. 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

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

Degree: PhD, University of Delaware, Department of Chemical and Biomolecular Engineering, 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 March 04, 2021. 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. 04 Mar 2021.

Vancouver:

O'Brien CJ. Colloidal protein-protein interactions as a design target for aggregation resistance. [Internet] [Doctoral dissertation]. University of Delaware; 2018. [cited 2021 Mar 04]. 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


University of Maryland

7. Motabar, Dana. THE DESIGN OF TWO PROTEINS THAT HAVE 100% SEQUENCE IDENTITY BUT ENCODE DIFFERENT FOLDS.

Degree: Bioengineering, 2015, University of Maryland

 It is well-established that proteins adopt specific three-dimensional structures. However, examples of proteins that can adopt more than one folded state have become increasingly more… (more)

Subjects/Keywords: Biomedical engineering; Protein Design; Protein Engineering; Protein Evolution

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APA (6th Edition):

Motabar, D. (2015). THE DESIGN OF TWO PROTEINS THAT HAVE 100% SEQUENCE IDENTITY BUT ENCODE DIFFERENT FOLDS. (Thesis). University of Maryland. Retrieved from http://hdl.handle.net/1903/17377

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):

Motabar, Dana. “THE DESIGN OF TWO PROTEINS THAT HAVE 100% SEQUENCE IDENTITY BUT ENCODE DIFFERENT FOLDS.” 2015. Thesis, University of Maryland. Accessed March 04, 2021. http://hdl.handle.net/1903/17377.

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

MLA Handbook (7th Edition):

Motabar, Dana. “THE DESIGN OF TWO PROTEINS THAT HAVE 100% SEQUENCE IDENTITY BUT ENCODE DIFFERENT FOLDS.” 2015. Web. 04 Mar 2021.

Vancouver:

Motabar D. THE DESIGN OF TWO PROTEINS THAT HAVE 100% SEQUENCE IDENTITY BUT ENCODE DIFFERENT FOLDS. [Internet] [Thesis]. University of Maryland; 2015. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/1903/17377.

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

Council of Science Editors:

Motabar D. THE DESIGN OF TWO PROTEINS THAT HAVE 100% SEQUENCE IDENTITY BUT ENCODE DIFFERENT FOLDS. [Thesis]. University of Maryland; 2015. Available from: http://hdl.handle.net/1903/17377

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


University of Canterbury

8. Littlejohn, Jacob James. Peroxiredoxins : a model for a self-assembling nanoscale system.

Degree: MS, Biological Sciences, 2012, University of Canterbury

 The formation of large, complex structures from small building blocks through self-assembly is widely seen in proteins and provides a tool for the creation of… (more)

Subjects/Keywords: peroxiredoxin; protein; self-assembly; protein engineering

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APA (6th Edition):

Littlejohn, J. J. (2012). Peroxiredoxins : a model for a self-assembling nanoscale system. (Masters Thesis). University of Canterbury. Retrieved from http://dx.doi.org/10.26021/5926

Chicago Manual of Style (16th Edition):

Littlejohn, Jacob James. “Peroxiredoxins : a model for a self-assembling nanoscale system.” 2012. Masters Thesis, University of Canterbury. Accessed March 04, 2021. http://dx.doi.org/10.26021/5926.

MLA Handbook (7th Edition):

Littlejohn, Jacob James. “Peroxiredoxins : a model for a self-assembling nanoscale system.” 2012. Web. 04 Mar 2021.

Vancouver:

Littlejohn JJ. Peroxiredoxins : a model for a self-assembling nanoscale system. [Internet] [Masters thesis]. University of Canterbury; 2012. [cited 2021 Mar 04]. Available from: http://dx.doi.org/10.26021/5926.

Council of Science Editors:

Littlejohn JJ. Peroxiredoxins : a model for a self-assembling nanoscale system. [Masters Thesis]. University of Canterbury; 2012. Available from: http://dx.doi.org/10.26021/5926


Vanderbilt University

9. Duran, Amanda Marie. Improving membrane protein modeling and design using empirical data.

Degree: PhD, Chemistry, 2018, Vanderbilt University

 Membrane proteins are an important class of proteins that represent approximately 30% of the open reading frame. However, due to their inherent flexibility, membrane proteins… (more)

Subjects/Keywords: computational design; comparative modeling; protein engineering; protein design; membrane protein

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APA (6th Edition):

Duran, A. M. (2018). Improving membrane protein modeling and design using empirical data. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/15387

Chicago Manual of Style (16th Edition):

Duran, Amanda Marie. “Improving membrane protein modeling and design using empirical data.” 2018. Doctoral Dissertation, Vanderbilt University. Accessed March 04, 2021. http://hdl.handle.net/1803/15387.

MLA Handbook (7th Edition):

Duran, Amanda Marie. “Improving membrane protein modeling and design using empirical data.” 2018. Web. 04 Mar 2021.

Vancouver:

Duran AM. Improving membrane protein modeling and design using empirical data. [Internet] [Doctoral dissertation]. Vanderbilt University; 2018. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/1803/15387.

Council of Science Editors:

Duran AM. Improving membrane protein modeling and design using empirical data. [Doctoral Dissertation]. Vanderbilt University; 2018. Available from: http://hdl.handle.net/1803/15387


University of California – San Diego

10. 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 March 04, 2021. 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. 04 Mar 2021.

Vancouver:

Maniaci BM. Design of Metal-Controlled Protein-Protein Interactions. [Internet] [Thesis]. University of California – San Diego; 2019. [cited 2021 Mar 04]. 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 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 March 04, 2021. 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. 04 Mar 2021.

Vancouver:

Barrett JR. Pragmatic protein domain identification. [Internet] [Doctoral dissertation]. University of Wollongong; 2014. [cited 2021 Mar 04]. 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


Rice University

12. 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 March 04, 2021. 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. 04 Mar 2021.

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 2021 Mar 04]. 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


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 March 04, 2021. http://arks.princeton.edu/ark:/88435/dsp01f1881p574.

MLA Handbook (7th Edition):

Stevens, Adam Joseph. “Discovery, Design, and Deployment of Enhanced Split Inteins .” 2018. Web. 04 Mar 2021.

Vancouver:

Stevens AJ. Discovery, Design, and Deployment of Enhanced Split Inteins . [Internet] [Doctoral dissertation]. Princeton University; 2018. [cited 2021 Mar 04]. 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


The Ohio State University

14. 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 March 04, 2021. 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. 04 Mar 2021.

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 2021 Mar 04]. 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


Columbia University

15. 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 March 04, 2021. https://doi.org/10.7916/D80002NC.

MLA Handbook (7th Edition):

Bulutoglu, Beyza. “Engineering Biomolecular Interfaces for Applications in Biotechnology.” 2017. Web. 04 Mar 2021.

Vancouver:

Bulutoglu B. Engineering Biomolecular Interfaces for Applications in Biotechnology. [Internet] [Doctoral dissertation]. Columbia University; 2017. [cited 2021 Mar 04]. 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

16. 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 March 04, 2021. 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. 04 Mar 2021.

Vancouver:

Davey JA. Multistate Computational Protein Design: Theories, Methods, and Applications . [Internet] [Thesis]. University of Ottawa; 2016. [cited 2021 Mar 04]. 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

17. 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 (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 March 04, 2021. 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. 04 Mar 2021.

Vancouver:

Chen H. Deconstruction and reconstruction of a protein capsid. [Internet] [Doctoral dissertation]. University of Utah; 2014. [cited 2021 Mar 04]. 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


Cornell University

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

Degree: PhD, Biomedical Engineering, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/40952

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. Doctoral Dissertation, Cornell University. Accessed March 04, 2021. http://hdl.handle.net/1813/40952.

MLA Handbook (7th Edition):

Lata, James. “Engineering A Rapid Point-Of-Care Diagnostic Platform Utilizing Tethered Enzyme Technology For Time-Sensitive Pathologies.” 2015. Web. 04 Mar 2021.

Vancouver:

Lata J. Engineering A Rapid Point-Of-Care Diagnostic Platform Utilizing Tethered Enzyme Technology For Time-Sensitive Pathologies. [Internet] [Doctoral dissertation]. Cornell University; 2015. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/1813/40952.

Council of Science Editors:

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


Cornell University

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

Degree: PhD, Chemical Engineering, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/29502

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. Doctoral Dissertation, Cornell University. Accessed March 04, 2021. http://hdl.handle.net/1813/29502.

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. 04 Mar 2021.

Vancouver:

Mansell T. A Suite Of Tools For Reporting And Engineering Protein Folding, Interactions, And Post-Translational Modifications In The Bacterial Periplasm. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/1813/29502.

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. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/29502


Texas A&M University

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

Degree: PhD, Toxicology, 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. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/149

Chicago Manual of Style (16th Edition):

Lum, Karin Tien. “Directed evolution of phosphotriesterase: towards the efficient detoxification of sarin and soman.” 2004. Doctoral Dissertation, Texas A&M University. Accessed March 04, 2021. http://hdl.handle.net/1969.1/149.

MLA Handbook (7th Edition):

Lum, Karin Tien. “Directed evolution of phosphotriesterase: towards the efficient detoxification of sarin and soman.” 2004. Web. 04 Mar 2021.

Vancouver:

Lum KT. Directed evolution of phosphotriesterase: towards the efficient detoxification of sarin and soman. [Internet] [Doctoral dissertation]. Texas A&M University; 2004. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/1969.1/149.

Council of Science Editors:

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


University of Colorado

21. 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 March 04, 2021. 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. 04 Mar 2021.

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 2021 Mar 04]. 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


University of Manchester

22. 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 March 04, 2021. 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. 04 Mar 2021.

Vancouver:

Hugentobler K. Development of new biocatalytic routes to pharmaceutical intermediates : a case study on Ticagrelor. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2021 Mar 04]. 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


Montana State University

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

Degree: PhD, 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. (Doctoral Dissertation). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/9137

Chicago Manual of Style (16th Edition):

Servid, Amy Eloise. “Characterization and embellishment of protein cages for nanomedical and nanomaterial applications.” 2014. Doctoral Dissertation, Montana State University. Accessed March 04, 2021. https://scholarworks.montana.edu/xmlui/handle/1/9137.

MLA Handbook (7th Edition):

Servid, Amy Eloise. “Characterization and embellishment of protein cages for nanomedical and nanomaterial applications.” 2014. Web. 04 Mar 2021.

Vancouver:

Servid AE. Characterization and embellishment of protein cages for nanomedical and nanomaterial applications. [Internet] [Doctoral dissertation]. Montana State University; 2014. [cited 2021 Mar 04]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/9137.

Council of Science Editors:

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


University of Toronto

24. Alhaeri, Maryam Foumani. Engineering and Production of Glucooligosaccharide Oxidases for Site-specific Activation of Cellulose and Hemicellulose Substrates.

Degree: PhD, 2015, University of Toronto

 Canada has an extensive supply of residual biomass, which comprises plant polysaccharides that represent a renewable resource for the production of biochemicals, polymers and fuels.… (more)

Subjects/Keywords: Enzymatic Oxidation; Protein Engineering; 0542

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APA (6th Edition):

Alhaeri, M. F. (2015). Engineering and Production of Glucooligosaccharide Oxidases for Site-specific Activation of Cellulose and Hemicellulose Substrates. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/70793

Chicago Manual of Style (16th Edition):

Alhaeri, Maryam Foumani. “Engineering and Production of Glucooligosaccharide Oxidases for Site-specific Activation of Cellulose and Hemicellulose Substrates.” 2015. Doctoral Dissertation, University of Toronto. Accessed March 04, 2021. http://hdl.handle.net/1807/70793.

MLA Handbook (7th Edition):

Alhaeri, Maryam Foumani. “Engineering and Production of Glucooligosaccharide Oxidases for Site-specific Activation of Cellulose and Hemicellulose Substrates.” 2015. Web. 04 Mar 2021.

Vancouver:

Alhaeri MF. Engineering and Production of Glucooligosaccharide Oxidases for Site-specific Activation of Cellulose and Hemicellulose Substrates. [Internet] [Doctoral dissertation]. University of Toronto; 2015. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/1807/70793.

Council of Science Editors:

Alhaeri MF. Engineering and Production of Glucooligosaccharide Oxidases for Site-specific Activation of Cellulose and Hemicellulose Substrates. [Doctoral Dissertation]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/70793


University of Minnesota

25. 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 March 04, 2021. http://hdl.handle.net/11299/165590.

MLA Handbook (7th Edition):

Strange, Jacob. “Rational improvement of the activity of a nitrite reductase model.” 2014. Web. 04 Mar 2021.

Vancouver:

Strange J. Rational improvement of the activity of a nitrite reductase model. [Internet] [Masters thesis]. University of Minnesota; 2014. [cited 2021 Mar 04]. 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 Texas – Austin

26. 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 March 04, 2021. http://hdl.handle.net/2152/31292.

MLA Handbook (7th Edition):

Meyer, Adam Joshua. “The evolution and engineering of T7 RNA polymerase.” 2014. Web. 04 Mar 2021.

Vancouver:

Meyer AJ. The evolution and engineering of T7 RNA polymerase. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2021 Mar 04]. 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


Michigan State University

27. 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 March 04, 2021. 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. 04 Mar 2021.

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 2021 Mar 04]. 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


Michigan State University

28. Lee, Kin Sing Stephen. 1) Probing the wavelength regulation of rhodopsin pigments via de novo protein engineering of a rhodopsin mimic and; 2) Engineering CRABPII as a retinal isomerase and a protein fusion tag.

Degree: 2011, Michigan State University

Thesis Ph. D. Michigan State University. Chemistry 2011.

1) PROBING THE WAVELENGTH REGULATION OF RHODOPSIN PIGMENTS VIA DE NOVO PROTEIN ENGINEERING OF A RHODOPSIN… (more)

Subjects/Keywords: Protein engineering; Rhodopsin; Chemistry

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APA (6th Edition):

Lee, K. S. S. (2011). 1) Probing the wavelength regulation of rhodopsin pigments via de novo protein engineering of a rhodopsin mimic and; 2) Engineering CRABPII as a retinal isomerase and a protein fusion tag. (Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:705

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):

Lee, Kin Sing Stephen. “1) Probing the wavelength regulation of rhodopsin pigments via de novo protein engineering of a rhodopsin mimic and; 2) Engineering CRABPII as a retinal isomerase and a protein fusion tag.” 2011. Thesis, Michigan State University. Accessed March 04, 2021. http://etd.lib.msu.edu/islandora/object/etd:705.

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

MLA Handbook (7th Edition):

Lee, Kin Sing Stephen. “1) Probing the wavelength regulation of rhodopsin pigments via de novo protein engineering of a rhodopsin mimic and; 2) Engineering CRABPII as a retinal isomerase and a protein fusion tag.” 2011. Web. 04 Mar 2021.

Vancouver:

Lee KSS. 1) Probing the wavelength regulation of rhodopsin pigments via de novo protein engineering of a rhodopsin mimic and; 2) Engineering CRABPII as a retinal isomerase and a protein fusion tag. [Internet] [Thesis]. Michigan State University; 2011. [cited 2021 Mar 04]. Available from: http://etd.lib.msu.edu/islandora/object/etd:705.

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

Council of Science Editors:

Lee KSS. 1) Probing the wavelength regulation of rhodopsin pigments via de novo protein engineering of a rhodopsin mimic and; 2) Engineering CRABPII as a retinal isomerase and a protein fusion tag. [Thesis]. Michigan State University; 2011. Available from: http://etd.lib.msu.edu/islandora/object/etd:705

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


Rutgers University

29. 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 March 04, 2021. 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. 04 Mar 2021.

Vancouver:

Blacklock, Kristin 1. New tools and approaches for computational protein design. [Internet] [Doctoral dissertation]. Rutgers University; 2019. [cited 2021 Mar 04]. 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

30. 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 March 04, 2021. 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. 04 Mar 2021.

Vancouver:

Hernandez, Nancy 1. Towards overcoming the deficiencies of recently evolved biodegradative enzymes. [Internet] [Doctoral dissertation]. Rutgers University; 2019. [cited 2021 Mar 04]. 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/

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