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You searched for subject:(Protein engineering High throughput Stability Combinatorial library Antibodies). Showing records 1 – 30 of 273648 total matches.

[1] [2] [3] [4] [5] … [9122]

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The Ohio State University

1. Sen, Shiladitya. Engineering Proteins for Enhanced Stability using High-throughput and Combinatorial methods.

Degree: PhD, Chemistry, 2013, The Ohio State University

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

Subjects/Keywords: Chemistry; Biochemistry; Protein engineering, High-throughput, Stability, Combinatorial library,Antibodies

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

APA (6th Edition):

Sen, S. (2013). Engineering Proteins for Enhanced Stability using High-throughput and Combinatorial methods. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1385987653

Chicago Manual of Style (16th Edition):

Sen, Shiladitya. “Engineering Proteins for Enhanced Stability using High-throughput and Combinatorial methods.” 2013. Doctoral Dissertation, The Ohio State University. Accessed August 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1385987653.

MLA Handbook (7th Edition):

Sen, Shiladitya. “Engineering Proteins for Enhanced Stability using High-throughput and Combinatorial methods.” 2013. Web. 07 Aug 2020.

Vancouver:

Sen S. Engineering Proteins for Enhanced Stability using High-throughput and Combinatorial methods. [Internet] [Doctoral dissertation]. The Ohio State University; 2013. [cited 2020 Aug 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1385987653.

Council of Science Editors:

Sen S. Engineering Proteins for Enhanced Stability using High-throughput and Combinatorial methods. [Doctoral Dissertation]. The Ohio State University; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1385987653


The Ohio State University

2. Li, Weiyi. Protein Engineering Hydrophobic Core Residues of Computationally Designed Protein G and Single-Chain Rop: Investigating the Relationship between Protein Primary structure and Protein Stability through High-Throughput Approaches.

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

 The sequence-structure-stability relationship is a key problem in the field of protein science. Although a large amount of research has been working on it in… (more)

Subjects/Keywords: Biochemistry; Chemistry; Biophysics; Biology; Rop, Rosetta, protein G, combinatorial library, hydrophobic core library, computational design, high-throughput

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APA (6th Edition):

Li, W. (2014). Protein Engineering Hydrophobic Core Residues of Computationally Designed Protein G and Single-Chain Rop: Investigating the Relationship between Protein Primary structure and Protein Stability through High-Throughput Approaches. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1398956266

Chicago Manual of Style (16th Edition):

Li, Weiyi. “Protein Engineering Hydrophobic Core Residues of Computationally Designed Protein G and Single-Chain Rop: Investigating the Relationship between Protein Primary structure and Protein Stability through High-Throughput Approaches.” 2014. Masters Thesis, The Ohio State University. Accessed August 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1398956266.

MLA Handbook (7th Edition):

Li, Weiyi. “Protein Engineering Hydrophobic Core Residues of Computationally Designed Protein G and Single-Chain Rop: Investigating the Relationship between Protein Primary structure and Protein Stability through High-Throughput Approaches.” 2014. Web. 07 Aug 2020.

Vancouver:

Li W. Protein Engineering Hydrophobic Core Residues of Computationally Designed Protein G and Single-Chain Rop: Investigating the Relationship between Protein Primary structure and Protein Stability through High-Throughput Approaches. [Internet] [Masters thesis]. The Ohio State University; 2014. [cited 2020 Aug 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1398956266.

Council of Science Editors:

Li W. Protein Engineering Hydrophobic Core Residues of Computationally Designed Protein G and Single-Chain Rop: Investigating the Relationship between Protein Primary structure and Protein Stability through High-Throughput Approaches. [Masters Thesis]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1398956266


University of Pennsylvania

3. Brey, Darren M. Combinatorial Polymer Synthesis and High-Throughput Screening Technology to Identify Optimal Approaches for Mineralized Tissue Engineering.

Degree: 2010, University of Pennsylvania

 The general tissue engineering approach is to combine cells, scaffolding, and signaling molecules in a manner that treats damaged or diseased tissues. Progress in the… (more)

Subjects/Keywords: combinatorial library; high-throughput screening; mesenchymal stem cells; mineralization; bone tissue engineering; Biomaterials; Molecular, Cellular, and Tissue Engineering

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APA (6th Edition):

Brey, D. M. (2010). Combinatorial Polymer Synthesis and High-Throughput Screening Technology to Identify Optimal Approaches for Mineralized Tissue Engineering. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/230

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):

Brey, Darren M. “Combinatorial Polymer Synthesis and High-Throughput Screening Technology to Identify Optimal Approaches for Mineralized Tissue Engineering.” 2010. Thesis, University of Pennsylvania. Accessed August 07, 2020. https://repository.upenn.edu/edissertations/230.

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

MLA Handbook (7th Edition):

Brey, Darren M. “Combinatorial Polymer Synthesis and High-Throughput Screening Technology to Identify Optimal Approaches for Mineralized Tissue Engineering.” 2010. Web. 07 Aug 2020.

Vancouver:

Brey DM. Combinatorial Polymer Synthesis and High-Throughput Screening Technology to Identify Optimal Approaches for Mineralized Tissue Engineering. [Internet] [Thesis]. University of Pennsylvania; 2010. [cited 2020 Aug 07]. Available from: https://repository.upenn.edu/edissertations/230.

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

Council of Science Editors:

Brey DM. Combinatorial Polymer Synthesis and High-Throughput Screening Technology to Identify Optimal Approaches for Mineralized Tissue Engineering. [Thesis]. University of Pennsylvania; 2010. Available from: https://repository.upenn.edu/edissertations/230

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


University of Cambridge

4. Hours, Raphaelle. Directed evolution of amino acid dehydrogenases for biocatalysis of chiral amines.

Degree: PhD, 2018, University of Cambridge

 By applying the principles of Darwinian natural selection in the laboratory, directed evolution has become a powerful practical approach to study enzymes and optimize them… (more)

Subjects/Keywords: Directed evoluion; Protein engineering; Microfluidics; High throughput screening; Amino acid dehydrogenases; Biocatalysis; Enzyme stability

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APA (6th Edition):

Hours, R. (2018). Directed evolution of amino acid dehydrogenases for biocatalysis of chiral amines. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/275471 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744797

Chicago Manual of Style (16th Edition):

Hours, Raphaelle. “Directed evolution of amino acid dehydrogenases for biocatalysis of chiral amines.” 2018. Doctoral Dissertation, University of Cambridge. Accessed August 07, 2020. https://www.repository.cam.ac.uk/handle/1810/275471 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744797.

MLA Handbook (7th Edition):

Hours, Raphaelle. “Directed evolution of amino acid dehydrogenases for biocatalysis of chiral amines.” 2018. Web. 07 Aug 2020.

Vancouver:

Hours R. Directed evolution of amino acid dehydrogenases for biocatalysis of chiral amines. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2020 Aug 07]. Available from: https://www.repository.cam.ac.uk/handle/1810/275471 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744797.

Council of Science Editors:

Hours R. Directed evolution of amino acid dehydrogenases for biocatalysis of chiral amines. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/275471 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744797


Iowa State University

5. Petersen, Latrisha Kay. Combinatorial design and development of biomaterials for use as drug delivery devices and immune adjuvants.

Degree: 2011, Iowa State University

 There are several challenges associated with current strategies for drug and vaccine delivery. These include the need for multiple-dose administrations, which can hinder patience compliance,… (more)

Subjects/Keywords: adjuvants; combinatorial; high throughput; nanoparticles; polyanhydrides; vaccines; Biological Engineering; Chemical Engineering

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APA (6th Edition):

Petersen, L. K. (2011). Combinatorial design and development of biomaterials for use as drug delivery devices and immune adjuvants. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/11988

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):

Petersen, Latrisha Kay. “Combinatorial design and development of biomaterials for use as drug delivery devices and immune adjuvants.” 2011. Thesis, Iowa State University. Accessed August 07, 2020. https://lib.dr.iastate.edu/etd/11988.

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

MLA Handbook (7th Edition):

Petersen, Latrisha Kay. “Combinatorial design and development of biomaterials for use as drug delivery devices and immune adjuvants.” 2011. Web. 07 Aug 2020.

Vancouver:

Petersen LK. Combinatorial design and development of biomaterials for use as drug delivery devices and immune adjuvants. [Internet] [Thesis]. Iowa State University; 2011. [cited 2020 Aug 07]. Available from: https://lib.dr.iastate.edu/etd/11988.

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

Council of Science Editors:

Petersen LK. Combinatorial design and development of biomaterials for use as drug delivery devices and immune adjuvants. [Thesis]. Iowa State University; 2011. Available from: https://lib.dr.iastate.edu/etd/11988

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


Cornell University

6. Wong, Sharon. Probing the biophysical mechanisms of gene delivery by synthetic evolution of combinatorial polymeric vector libraries .

Degree: 2008, Cornell University

 The prospect of treating debilitating and even fatal diseases by way of genetic-based interventions has been the long-standing goal of gene therapy. However, its widespread… (more)

Subjects/Keywords: gene delivery; polymeric vectors; combinatorial library; high throughput

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APA (6th Edition):

Wong, S. (2008). Probing the biophysical mechanisms of gene delivery by synthetic evolution of combinatorial polymeric vector libraries . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/10868

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):

Wong, Sharon. “Probing the biophysical mechanisms of gene delivery by synthetic evolution of combinatorial polymeric vector libraries .” 2008. Thesis, Cornell University. Accessed August 07, 2020. http://hdl.handle.net/1813/10868.

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

MLA Handbook (7th Edition):

Wong, Sharon. “Probing the biophysical mechanisms of gene delivery by synthetic evolution of combinatorial polymeric vector libraries .” 2008. Web. 07 Aug 2020.

Vancouver:

Wong S. Probing the biophysical mechanisms of gene delivery by synthetic evolution of combinatorial polymeric vector libraries . [Internet] [Thesis]. Cornell University; 2008. [cited 2020 Aug 07]. Available from: http://hdl.handle.net/1813/10868.

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

Council of Science Editors:

Wong S. Probing the biophysical mechanisms of gene delivery by synthetic evolution of combinatorial polymeric vector libraries . [Thesis]. Cornell University; 2008. Available from: http://hdl.handle.net/1813/10868

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


University of Kansas

7. Imaduwage, Kasun Prabodha. High-Throughput Screening (HTS) of Potential Lead Compounds for Target Proteins with No False Identifications Using LC/MS.

Degree: PhD, Chemistry, 2017, University of Kansas

 Developing effective high throughput screening (HTS) methods is of paramount importance in the early stage of drug discovery. When a protein binding event can be… (more)

Subjects/Keywords: Chemistry; false negatives; false positives; High throughput screening; LC/MS; library compounds; Target protein

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APA (6th Edition):

Imaduwage, K. P. (2017). High-Throughput Screening (HTS) of Potential Lead Compounds for Target Proteins with No False Identifications Using LC/MS. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/26012

Chicago Manual of Style (16th Edition):

Imaduwage, Kasun Prabodha. “High-Throughput Screening (HTS) of Potential Lead Compounds for Target Proteins with No False Identifications Using LC/MS.” 2017. Doctoral Dissertation, University of Kansas. Accessed August 07, 2020. http://hdl.handle.net/1808/26012.

MLA Handbook (7th Edition):

Imaduwage, Kasun Prabodha. “High-Throughput Screening (HTS) of Potential Lead Compounds for Target Proteins with No False Identifications Using LC/MS.” 2017. Web. 07 Aug 2020.

Vancouver:

Imaduwage KP. High-Throughput Screening (HTS) of Potential Lead Compounds for Target Proteins with No False Identifications Using LC/MS. [Internet] [Doctoral dissertation]. University of Kansas; 2017. [cited 2020 Aug 07]. Available from: http://hdl.handle.net/1808/26012.

Council of Science Editors:

Imaduwage KP. High-Throughput Screening (HTS) of Potential Lead Compounds for Target Proteins with No False Identifications Using LC/MS. [Doctoral Dissertation]. University of Kansas; 2017. Available from: http://hdl.handle.net/1808/26012


University of Sydney

8. Reslan, Mouhamad. Development of Aggregation-Resistant Monoclonal Antibodies Through Antibody Engineering and Formulation Approaches .

Degree: 2018, University of Sydney

 Monoclonal antibodies (mAbs) are invaluable in the treatment of cancers, auto-immune and inflammatory conditions. Since their advent, approximately 80 mAbs and antibody-based therapeutic products have… (more)

Subjects/Keywords: monoclonal antibodies; stability; protein aggregation; formulation; antibody engineering; biotechnology

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APA (6th Edition):

Reslan, M. (2018). Development of Aggregation-Resistant Monoclonal Antibodies Through Antibody Engineering and Formulation Approaches . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/19700

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):

Reslan, Mouhamad. “Development of Aggregation-Resistant Monoclonal Antibodies Through Antibody Engineering and Formulation Approaches .” 2018. Thesis, University of Sydney. Accessed August 07, 2020. http://hdl.handle.net/2123/19700.

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

MLA Handbook (7th Edition):

Reslan, Mouhamad. “Development of Aggregation-Resistant Monoclonal Antibodies Through Antibody Engineering and Formulation Approaches .” 2018. Web. 07 Aug 2020.

Vancouver:

Reslan M. Development of Aggregation-Resistant Monoclonal Antibodies Through Antibody Engineering and Formulation Approaches . [Internet] [Thesis]. University of Sydney; 2018. [cited 2020 Aug 07]. Available from: http://hdl.handle.net/2123/19700.

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

Council of Science Editors:

Reslan M. Development of Aggregation-Resistant Monoclonal Antibodies Through Antibody Engineering and Formulation Approaches . [Thesis]. University of Sydney; 2018. Available from: http://hdl.handle.net/2123/19700

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


Univerzitet u Beogradu

9. Kovačević, Gordana N., 1987-. Proteinski inženjering i razvoj visoko efikasnih metoda za pretraživanje biblioteke gena glukoza-oksidaze iz Aspergillus niger u cilju povećanja enzimske aktivnosti i stabilnosti.

Degree: Hemijski fakultet, 2019, Univerzitet u Beogradu

Hemija - Biohemija / Chemistry - Biochemistry

Glukoza-oksidaza (GOx) je vaţan industrijski enzim koji se predominantno koristi kao biokatalizator u industriji hrane za proizvodnju glukonske… (more)

Subjects/Keywords: glucose oxidase; high-throughput screening; oxidative stability; yeast surface display; green fluorescent protein; Pichia pastoris

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APA (6th Edition):

Kovačević, Gordana N., 1. (2019). Proteinski inženjering i razvoj visoko efikasnih metoda za pretraživanje biblioteke gena glukoza-oksidaze iz Aspergillus niger u cilju povećanja enzimske aktivnosti i stabilnosti. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:19139/bdef:Content/get

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):

Kovačević, Gordana N., 1987-. “Proteinski inženjering i razvoj visoko efikasnih metoda za pretraživanje biblioteke gena glukoza-oksidaze iz Aspergillus niger u cilju povećanja enzimske aktivnosti i stabilnosti.” 2019. Thesis, Univerzitet u Beogradu. Accessed August 07, 2020. https://fedorabg.bg.ac.rs/fedora/get/o:19139/bdef:Content/get.

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

MLA Handbook (7th Edition):

Kovačević, Gordana N., 1987-. “Proteinski inženjering i razvoj visoko efikasnih metoda za pretraživanje biblioteke gena glukoza-oksidaze iz Aspergillus niger u cilju povećanja enzimske aktivnosti i stabilnosti.” 2019. Web. 07 Aug 2020.

Vancouver:

Kovačević, Gordana N. 1. Proteinski inženjering i razvoj visoko efikasnih metoda za pretraživanje biblioteke gena glukoza-oksidaze iz Aspergillus niger u cilju povećanja enzimske aktivnosti i stabilnosti. [Internet] [Thesis]. Univerzitet u Beogradu; 2019. [cited 2020 Aug 07]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:19139/bdef:Content/get.

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

Council of Science Editors:

Kovačević, Gordana N. 1. Proteinski inženjering i razvoj visoko efikasnih metoda za pretraživanje biblioteke gena glukoza-oksidaze iz Aspergillus niger u cilju povećanja enzimske aktivnosti i stabilnosti. [Thesis]. Univerzitet u Beogradu; 2019. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:19139/bdef:Content/get

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


Freie Universität Berlin

10. Schellenberg, Katja. Eine Hochdurchsatz-Analyse zirkadianer Proteinstabilität.

Degree: 2014, Freie Universität Berlin

 Circadiane Uhren sind endogen getriebene Oszillationen, welche 24-Stunden Rhythmen der Physiologie und des Verhaltens steuern. Circadiane Rhythmen existieren in nahezu allen Zellen des Körpers und… (more)

Subjects/Keywords: circadian; protein stability; high-throughput; 500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::572 Biochemie

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APA (6th Edition):

Schellenberg, K. (2014). Eine Hochdurchsatz-Analyse zirkadianer Proteinstabilität. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/12250

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):

Schellenberg, Katja. “Eine Hochdurchsatz-Analyse zirkadianer Proteinstabilität.” 2014. Thesis, Freie Universität Berlin. Accessed August 07, 2020. https://refubium.fu-berlin.de/handle/fub188/12250.

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

MLA Handbook (7th Edition):

Schellenberg, Katja. “Eine Hochdurchsatz-Analyse zirkadianer Proteinstabilität.” 2014. Web. 07 Aug 2020.

Vancouver:

Schellenberg K. Eine Hochdurchsatz-Analyse zirkadianer Proteinstabilität. [Internet] [Thesis]. Freie Universität Berlin; 2014. [cited 2020 Aug 07]. Available from: https://refubium.fu-berlin.de/handle/fub188/12250.

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

Council of Science Editors:

Schellenberg K. Eine Hochdurchsatz-Analyse zirkadianer Proteinstabilität. [Thesis]. Freie Universität Berlin; 2014. Available from: https://refubium.fu-berlin.de/handle/fub188/12250

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


University of Minnesota

11. Woldring, Daniel. Constrained Diversification Enhances Protein Ligand Discovery and Evolution.

Degree: PhD, Chemical Engineering, 2017, University of Minnesota

 Engineered proteins have strongly benefited the effectiveness and variety of precision drugs, molecular diagnostic agents, and fundamental research reagents. A growing demand for new therapeutics… (more)

Subjects/Keywords: computational biology; deep sequencing; library design; protein engineering; protein-protein interaction; stability engineering

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APA (6th Edition):

Woldring, D. (2017). Constrained Diversification Enhances Protein Ligand Discovery and Evolution. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/191350

Chicago Manual of Style (16th Edition):

Woldring, Daniel. “Constrained Diversification Enhances Protein Ligand Discovery and Evolution.” 2017. Doctoral Dissertation, University of Minnesota. Accessed August 07, 2020. http://hdl.handle.net/11299/191350.

MLA Handbook (7th Edition):

Woldring, Daniel. “Constrained Diversification Enhances Protein Ligand Discovery and Evolution.” 2017. Web. 07 Aug 2020.

Vancouver:

Woldring D. Constrained Diversification Enhances Protein Ligand Discovery and Evolution. [Internet] [Doctoral dissertation]. University of Minnesota; 2017. [cited 2020 Aug 07]. Available from: http://hdl.handle.net/11299/191350.

Council of Science Editors:

Woldring D. Constrained Diversification Enhances Protein Ligand Discovery and Evolution. [Doctoral Dissertation]. University of Minnesota; 2017. Available from: http://hdl.handle.net/11299/191350


KTH

12. Hendrikse, Natalie. Development of a Novel Selection Method for Protease Engineering : A high-throughput fluorescent reporter-based method for characterization and selection of proteases.

Degree: Technology and Health (STH), 2016, KTH

  Proteases are crucial to many biological processes and have become an important field of biomedical and biotechnological research. Engineering of proteases towards therapeutic applications… (more)

Subjects/Keywords: protein engineering; protease engineering; high-throughput selection method; fluorescent reporter

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APA (6th Edition):

Hendrikse, N. (2016). Development of a Novel Selection Method for Protease Engineering : A high-throughput fluorescent reporter-based method for characterization and selection of proteases. (Thesis). KTH. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-189227

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):

Hendrikse, Natalie. “Development of a Novel Selection Method for Protease Engineering : A high-throughput fluorescent reporter-based method for characterization and selection of proteases.” 2016. Thesis, KTH. Accessed August 07, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-189227.

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

MLA Handbook (7th Edition):

Hendrikse, Natalie. “Development of a Novel Selection Method for Protease Engineering : A high-throughput fluorescent reporter-based method for characterization and selection of proteases.” 2016. Web. 07 Aug 2020.

Vancouver:

Hendrikse N. Development of a Novel Selection Method for Protease Engineering : A high-throughput fluorescent reporter-based method for characterization and selection of proteases. [Internet] [Thesis]. KTH; 2016. [cited 2020 Aug 07]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-189227.

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

Council of Science Editors:

Hendrikse N. Development of a Novel Selection Method for Protease Engineering : A high-throughput fluorescent reporter-based method for characterization and selection of proteases. [Thesis]. KTH; 2016. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-189227

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


University of Illinois – Urbana-Champaign

13. Tang, Weng Lin. Engineering of an efficient and enantioselective biocatalyst for the preparation of chiral pharmaceutical intermediates.

Degree: PhD, 0300, 2011, University of Illinois – Urbana-Champaign

 This Ph.D. thesis focuses on the engineering of an efficient and enantioselective biocatalyst via direct evolution and genetic engineering for the enantioselective hydroxylation of non-activated… (more)

Subjects/Keywords: Directed Evolution; P450; High throughput screening; protein engineering

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APA (6th Edition):

Tang, W. L. (2011). Engineering of an efficient and enantioselective biocatalyst for the preparation of chiral pharmaceutical intermediates. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/26297

Chicago Manual of Style (16th Edition):

Tang, Weng Lin. “Engineering of an efficient and enantioselective biocatalyst for the preparation of chiral pharmaceutical intermediates.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 07, 2020. http://hdl.handle.net/2142/26297.

MLA Handbook (7th Edition):

Tang, Weng Lin. “Engineering of an efficient and enantioselective biocatalyst for the preparation of chiral pharmaceutical intermediates.” 2011. Web. 07 Aug 2020.

Vancouver:

Tang WL. Engineering of an efficient and enantioselective biocatalyst for the preparation of chiral pharmaceutical intermediates. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2020 Aug 07]. Available from: http://hdl.handle.net/2142/26297.

Council of Science Editors:

Tang WL. Engineering of an efficient and enantioselective biocatalyst for the preparation of chiral pharmaceutical intermediates. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/26297


University of Cambridge

14. Chong, Zheng Shan. Extracellular interaction screening using CRISPR activation.

Degree: PhD, 2019, University of Cambridge

 Extracellular interactions between cell surface receptors are necessary for signaling and adhesion but identifying them remains technically challenging. We describe a cell-based genome-wide approach employing… (more)

Subjects/Keywords: CRISPR; protein-protein interactions; high-throughput screening

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APA (6th Edition):

Chong, Z. S. (2019). Extracellular interaction screening using CRISPR activation. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/291972 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774750

Chicago Manual of Style (16th Edition):

Chong, Zheng Shan. “Extracellular interaction screening using CRISPR activation.” 2019. Doctoral Dissertation, University of Cambridge. Accessed August 07, 2020. https://www.repository.cam.ac.uk/handle/1810/291972 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774750.

MLA Handbook (7th Edition):

Chong, Zheng Shan. “Extracellular interaction screening using CRISPR activation.” 2019. Web. 07 Aug 2020.

Vancouver:

Chong ZS. Extracellular interaction screening using CRISPR activation. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Aug 07]. Available from: https://www.repository.cam.ac.uk/handle/1810/291972 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774750.

Council of Science Editors:

Chong ZS. Extracellular interaction screening using CRISPR activation. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/291972 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774750


University of Washington

15. Younger, David Aaron. High-Throughput Characterization of Protein-Protein Interactions by Reprogramming Yeast Mating.

Degree: PhD, 2017, University of Washington

High-throughput methods for screening protein-protein interactions enable the rapid characterization of engineered binding proteins and interaction networks. While existing approaches are powerful, none allow quantitative… (more)

Subjects/Keywords: High-throughput screening; Protein Engineering; Protein-protein interaction networks; Synthetic Biology; Yeast Mating; Biomedical engineering; Biochemistry; Cellular biology; Bioengineering

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APA (6th Edition):

Younger, D. A. (2017). High-Throughput Characterization of Protein-Protein Interactions by Reprogramming Yeast Mating. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/40488

Chicago Manual of Style (16th Edition):

Younger, David Aaron. “High-Throughput Characterization of Protein-Protein Interactions by Reprogramming Yeast Mating.” 2017. Doctoral Dissertation, University of Washington. Accessed August 07, 2020. http://hdl.handle.net/1773/40488.

MLA Handbook (7th Edition):

Younger, David Aaron. “High-Throughput Characterization of Protein-Protein Interactions by Reprogramming Yeast Mating.” 2017. Web. 07 Aug 2020.

Vancouver:

Younger DA. High-Throughput Characterization of Protein-Protein Interactions by Reprogramming Yeast Mating. [Internet] [Doctoral dissertation]. University of Washington; 2017. [cited 2020 Aug 07]. Available from: http://hdl.handle.net/1773/40488.

Council of Science Editors:

Younger DA. High-Throughput Characterization of Protein-Protein Interactions by Reprogramming Yeast Mating. [Doctoral Dissertation]. University of Washington; 2017. Available from: http://hdl.handle.net/1773/40488


Cornell University

16. Tague, Michele. A Combinatorial Approach For Exploring Fuel Cell Electrocatalysts .

Degree: 2011, Cornell University

 Fuel cells represent an alternative energy technology with the potential for providing more efficient means for energy conversion. However, their widespread deployment has been hampered… (more)

Subjects/Keywords: Methanol oxidation; fuel cells; Platinum alloys; combinatorial screening; Fluorescence; high throughput

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APA (6th Edition):

Tague, M. (2011). A Combinatorial Approach For Exploring Fuel Cell Electrocatalysts . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/30690

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):

Tague, Michele. “A Combinatorial Approach For Exploring Fuel Cell Electrocatalysts .” 2011. Thesis, Cornell University. Accessed August 07, 2020. http://hdl.handle.net/1813/30690.

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

MLA Handbook (7th Edition):

Tague, Michele. “A Combinatorial Approach For Exploring Fuel Cell Electrocatalysts .” 2011. Web. 07 Aug 2020.

Vancouver:

Tague M. A Combinatorial Approach For Exploring Fuel Cell Electrocatalysts . [Internet] [Thesis]. Cornell University; 2011. [cited 2020 Aug 07]. Available from: http://hdl.handle.net/1813/30690.

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

Council of Science Editors:

Tague M. A Combinatorial Approach For Exploring Fuel Cell Electrocatalysts . [Thesis]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/30690

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


University of Toronto

17. Economopoulos, Nicolas. The Generation of Affinity Reagents Using High-throughput Phage Display and Building the Foundations of a Novel High-throughput Intrabody Pipeline.

Degree: 2011, University of Toronto

Phage display technology has emerged as the dominant approach in antibody engineering. Here I describe my work in developing a high-throughput method of reliably generating… (more)

Subjects/Keywords: phage display; high-throughput; intrabody; antibody; intrabodies; antibodies; 0307

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APA (6th Edition):

Economopoulos, N. (2011). The Generation of Affinity Reagents Using High-throughput Phage Display and Building the Foundations of a Novel High-throughput Intrabody Pipeline. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/30584

Chicago Manual of Style (16th Edition):

Economopoulos, Nicolas. “The Generation of Affinity Reagents Using High-throughput Phage Display and Building the Foundations of a Novel High-throughput Intrabody Pipeline.” 2011. Masters Thesis, University of Toronto. Accessed August 07, 2020. http://hdl.handle.net/1807/30584.

MLA Handbook (7th Edition):

Economopoulos, Nicolas. “The Generation of Affinity Reagents Using High-throughput Phage Display and Building the Foundations of a Novel High-throughput Intrabody Pipeline.” 2011. Web. 07 Aug 2020.

Vancouver:

Economopoulos N. The Generation of Affinity Reagents Using High-throughput Phage Display and Building the Foundations of a Novel High-throughput Intrabody Pipeline. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2020 Aug 07]. Available from: http://hdl.handle.net/1807/30584.

Council of Science Editors:

Economopoulos N. The Generation of Affinity Reagents Using High-throughput Phage Display and Building the Foundations of a Novel High-throughput Intrabody Pipeline. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/30584

18. Tsai, Peter Te-Chuan. High-throughput Exploration of Glass Formation via Laser Deposition and the Study of Heterogeneous Microstructure in a Bulk Metallic Glass Alloy.

Degree: PhD, Mechanical Engineering & Materials Science, 2016, Washington University in St. Louis

  Bulk metallic glasses are a relatively novel class of engineering alloys characterized by a "disordered" atomic structure devoid of long-range translational symmetry. Compared to… (more)

Subjects/Keywords: combinatorial; high-throughput; metallic glass; structural heterogeneity; Engineering

…December 2016 x Abstract of the Dissertation High-throughput Exploration of Glass Formation… …throughput combinatorial methodology was developed to expedite the discovery process of new bulk… …method allowed high-throughput measurement of the nucleation temperature (Tn) of all… …to measure nucleation temperatures in a high-throughput manner. (TPF)58. Among… …libraries fabricated via a combinatorial approach could serve as a template for the high… 

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APA (6th Edition):

Tsai, P. T. (2016). High-throughput Exploration of Glass Formation via Laser Deposition and the Study of Heterogeneous Microstructure in a Bulk Metallic Glass Alloy. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/eng_etds/211

Chicago Manual of Style (16th Edition):

Tsai, Peter Te-Chuan. “High-throughput Exploration of Glass Formation via Laser Deposition and the Study of Heterogeneous Microstructure in a Bulk Metallic Glass Alloy.” 2016. Doctoral Dissertation, Washington University in St. Louis. Accessed August 07, 2020. https://openscholarship.wustl.edu/eng_etds/211.

MLA Handbook (7th Edition):

Tsai, Peter Te-Chuan. “High-throughput Exploration of Glass Formation via Laser Deposition and the Study of Heterogeneous Microstructure in a Bulk Metallic Glass Alloy.” 2016. Web. 07 Aug 2020.

Vancouver:

Tsai PT. High-throughput Exploration of Glass Formation via Laser Deposition and the Study of Heterogeneous Microstructure in a Bulk Metallic Glass Alloy. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2016. [cited 2020 Aug 07]. Available from: https://openscholarship.wustl.edu/eng_etds/211.

Council of Science Editors:

Tsai PT. High-throughput Exploration of Glass Formation via Laser Deposition and the Study of Heterogeneous Microstructure in a Bulk Metallic Glass Alloy. [Doctoral Dissertation]. Washington University in St. Louis; 2016. Available from: https://openscholarship.wustl.edu/eng_etds/211


The Ohio State University

19. 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 August 07, 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. 07 Aug 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 Aug 07]. 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


Texas A&M University

20. Haynes, Abria R. Characterization of Extremophilic Bacteria for Potential in the Biofuel and Bioprocess Industries.

Degree: 2014, Texas A&M University

 Industrial bioprocesses are constrained by the availability of microbes that are optimized for harsh bioprocess conditions. Over 500 soil and sediment samples collected from 77… (more)

Subjects/Keywords: Bacillus; High-Throughput Screening; Biofuels; Bacterial Library; Environmental Isolates

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APA (6th Edition):

Haynes, A. R. (2014). Characterization of Extremophilic Bacteria for Potential in the Biofuel and Bioprocess Industries. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/152602

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):

Haynes, Abria R. “Characterization of Extremophilic Bacteria for Potential in the Biofuel and Bioprocess Industries.” 2014. Thesis, Texas A&M University. Accessed August 07, 2020. http://hdl.handle.net/1969.1/152602.

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

MLA Handbook (7th Edition):

Haynes, Abria R. “Characterization of Extremophilic Bacteria for Potential in the Biofuel and Bioprocess Industries.” 2014. Web. 07 Aug 2020.

Vancouver:

Haynes AR. Characterization of Extremophilic Bacteria for Potential in the Biofuel and Bioprocess Industries. [Internet] [Thesis]. Texas A&M University; 2014. [cited 2020 Aug 07]. Available from: http://hdl.handle.net/1969.1/152602.

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

Council of Science Editors:

Haynes AR. Characterization of Extremophilic Bacteria for Potential in the Biofuel and Bioprocess Industries. [Thesis]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/152602

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


Rutgers University

21. Inoyama, Daigo, 1981-. The discovery of small-molecule inhibitors of keap1-nrf2 interaction with homogeneous fluorescence-based high throughput screening assays.

Degree: PhD, Medicinal Chemistry, 2014, Rutgers University

Keap1-Nrf2 interaction is a key protein-protein interaction involved in the activation of antioxidant response element which regulates the expression of cytoprotective enzymes in response to… (more)

Subjects/Keywords: Protein-protein interactions; High throughput screening (Drug development)

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APA (6th Edition):

Inoyama, Daigo, 1. (2014). The discovery of small-molecule inhibitors of keap1-nrf2 interaction with homogeneous fluorescence-based high throughput screening assays. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/45302/

Chicago Manual of Style (16th Edition):

Inoyama, Daigo, 1981-. “The discovery of small-molecule inhibitors of keap1-nrf2 interaction with homogeneous fluorescence-based high throughput screening assays.” 2014. Doctoral Dissertation, Rutgers University. Accessed August 07, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/45302/.

MLA Handbook (7th Edition):

Inoyama, Daigo, 1981-. “The discovery of small-molecule inhibitors of keap1-nrf2 interaction with homogeneous fluorescence-based high throughput screening assays.” 2014. Web. 07 Aug 2020.

Vancouver:

Inoyama, Daigo 1. The discovery of small-molecule inhibitors of keap1-nrf2 interaction with homogeneous fluorescence-based high throughput screening assays. [Internet] [Doctoral dissertation]. Rutgers University; 2014. [cited 2020 Aug 07]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/45302/.

Council of Science Editors:

Inoyama, Daigo 1. The discovery of small-molecule inhibitors of keap1-nrf2 interaction with homogeneous fluorescence-based high throughput screening assays. [Doctoral Dissertation]. Rutgers University; 2014. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/45302/


University of Oulu

22. Casteleijn, M. G. (Marinus G.). Towards new enzymes:protein engineering versus bioinformatic studies.

Degree: 2010, University of Oulu

 Abstract The aim of this PhD-study was to address some of the overlapping bottlenecks in protein engineering and metagenomics by developing or applying new tools… (more)

Subjects/Keywords: TIM; UP; biocatalyst; bioinformatics; enzyme; high throughput; kinetic studies; metagenomics; protein engineering; triosephosphate isomerase; uridine phosphorylase

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APA (6th Edition):

Casteleijn, M. G. (. G. ). (2010). Towards new enzymes:protein engineering versus bioinformatic studies. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789514260995

Chicago Manual of Style (16th Edition):

Casteleijn, M G (Marinus G ). “Towards new enzymes:protein engineering versus bioinformatic studies.” 2010. Doctoral Dissertation, University of Oulu. Accessed August 07, 2020. http://urn.fi/urn:isbn:9789514260995.

MLA Handbook (7th Edition):

Casteleijn, M G (Marinus G ). “Towards new enzymes:protein engineering versus bioinformatic studies.” 2010. Web. 07 Aug 2020.

Vancouver:

Casteleijn MG(G). Towards new enzymes:protein engineering versus bioinformatic studies. [Internet] [Doctoral dissertation]. University of Oulu; 2010. [cited 2020 Aug 07]. Available from: http://urn.fi/urn:isbn:9789514260995.

Council of Science Editors:

Casteleijn MG(G). Towards new enzymes:protein engineering versus bioinformatic studies. [Doctoral Dissertation]. University of Oulu; 2010. Available from: http://urn.fi/urn:isbn:9789514260995


Brigham Young University

23. Wilding, Kristen Michelle. Engineering Cell-Free Biosystems for On-Site Production and Rapid Design of Next-Generation Therapeutics.

Degree: PhD, 2018, Brigham Young University

 While protein therapeutics are indispensable in the treatment of a variety of diseases, including cancer, rheumatoid arthritis, and diabetes, key limitations including short half-lives, high(more)

Subjects/Keywords: synthetic biology; cell-free protein synthesis; endotoxin removal; lyophilization; lyoprotectant; unnatural amino acid; high-throughput screening; Engineering

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APA (6th Edition):

Wilding, K. M. (2018). Engineering Cell-Free Biosystems for On-Site Production and Rapid Design of Next-Generation Therapeutics. (Doctoral Dissertation). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=8713&context=etd

Chicago Manual of Style (16th Edition):

Wilding, Kristen Michelle. “Engineering Cell-Free Biosystems for On-Site Production and Rapid Design of Next-Generation Therapeutics.” 2018. Doctoral Dissertation, Brigham Young University. Accessed August 07, 2020. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=8713&context=etd.

MLA Handbook (7th Edition):

Wilding, Kristen Michelle. “Engineering Cell-Free Biosystems for On-Site Production and Rapid Design of Next-Generation Therapeutics.” 2018. Web. 07 Aug 2020.

Vancouver:

Wilding KM. Engineering Cell-Free Biosystems for On-Site Production and Rapid Design of Next-Generation Therapeutics. [Internet] [Doctoral dissertation]. Brigham Young University; 2018. [cited 2020 Aug 07]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=8713&context=etd.

Council of Science Editors:

Wilding KM. Engineering Cell-Free Biosystems for On-Site Production and Rapid Design of Next-Generation Therapeutics. [Doctoral Dissertation]. Brigham Young University; 2018. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=8713&context=etd


University of Kansas

24. Thomas, Justin Cody. Toward the Development of an Improved Ricin Vaccine.

Degree: PhD, Pharmaceutical Chemistry, 2013, University of Kansas

 To date, there is no approved antidote to treat or prevent the toxic effects of ricin exposure. RiVax, a recombinant ricin A chain subunit vaccine… (more)

Subjects/Keywords: Pharmaceutical sciences; antibodies; antigen; mutagenesis; protein stability; ricin toxin; vaccines

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APA (6th Edition):

Thomas, J. C. (2013). Toward the Development of an Improved Ricin Vaccine. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/21628

Chicago Manual of Style (16th Edition):

Thomas, Justin Cody. “Toward the Development of an Improved Ricin Vaccine.” 2013. Doctoral Dissertation, University of Kansas. Accessed August 07, 2020. http://hdl.handle.net/1808/21628.

MLA Handbook (7th Edition):

Thomas, Justin Cody. “Toward the Development of an Improved Ricin Vaccine.” 2013. Web. 07 Aug 2020.

Vancouver:

Thomas JC. Toward the Development of an Improved Ricin Vaccine. [Internet] [Doctoral dissertation]. University of Kansas; 2013. [cited 2020 Aug 07]. Available from: http://hdl.handle.net/1808/21628.

Council of Science Editors:

Thomas JC. Toward the Development of an Improved Ricin Vaccine. [Doctoral Dissertation]. University of Kansas; 2013. Available from: http://hdl.handle.net/1808/21628


University of Toronto

25. Yoo, Hayoung. Generation of Human Synthetic Antibodies against Frizzled-7 Receptor.

Degree: 2016, University of Toronto

Antibodies are the fastest growing class of therapeutic agents, capable of targeting diseased phenotypes with high affinity and specificity. Phage display technology was strategically utilized… (more)

Subjects/Keywords: Frizzled; High-throughput screening; monoclonal antibodies; phage display; Synthetic antibody; Wnt; 0572

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APA (6th Edition):

Yoo, H. (2016). Generation of Human Synthetic Antibodies against Frizzled-7 Receptor. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/72848

Chicago Manual of Style (16th Edition):

Yoo, Hayoung. “Generation of Human Synthetic Antibodies against Frizzled-7 Receptor.” 2016. Masters Thesis, University of Toronto. Accessed August 07, 2020. http://hdl.handle.net/1807/72848.

MLA Handbook (7th Edition):

Yoo, Hayoung. “Generation of Human Synthetic Antibodies against Frizzled-7 Receptor.” 2016. Web. 07 Aug 2020.

Vancouver:

Yoo H. Generation of Human Synthetic Antibodies against Frizzled-7 Receptor. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Aug 07]. Available from: http://hdl.handle.net/1807/72848.

Council of Science Editors:

Yoo H. Generation of Human Synthetic Antibodies against Frizzled-7 Receptor. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/72848


University of Edinburgh

26. Auxillos, Jamie Yam. Establishing a standardised DNA assembly and biosensor-based screening pipeline for natural product pathway engineering in Saccharomyces cerevisiae.

Degree: PhD, 2020, University of Edinburgh

 Many pharmaceutical drugs currently available on the market are natural products, which are extracted from biological sources (microorganisms or plants). It can prove challenging to… (more)

Subjects/Keywords: high-throughput; pathway engineering; yeast; biosensors

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APA (6th Edition):

Auxillos, J. Y. (2020). Establishing a standardised DNA assembly and biosensor-based screening pipeline for natural product pathway engineering in Saccharomyces cerevisiae. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/37035

Chicago Manual of Style (16th Edition):

Auxillos, Jamie Yam. “Establishing a standardised DNA assembly and biosensor-based screening pipeline for natural product pathway engineering in Saccharomyces cerevisiae.” 2020. Doctoral Dissertation, University of Edinburgh. Accessed August 07, 2020. http://hdl.handle.net/1842/37035.

MLA Handbook (7th Edition):

Auxillos, Jamie Yam. “Establishing a standardised DNA assembly and biosensor-based screening pipeline for natural product pathway engineering in Saccharomyces cerevisiae.” 2020. Web. 07 Aug 2020.

Vancouver:

Auxillos JY. Establishing a standardised DNA assembly and biosensor-based screening pipeline for natural product pathway engineering in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of Edinburgh; 2020. [cited 2020 Aug 07]. Available from: http://hdl.handle.net/1842/37035.

Council of Science Editors:

Auxillos JY. Establishing a standardised DNA assembly and biosensor-based screening pipeline for natural product pathway engineering in Saccharomyces cerevisiae. [Doctoral Dissertation]. University of Edinburgh; 2020. Available from: http://hdl.handle.net/1842/37035

27. Aviolat, Hubert. Development of new high-throughput technology and combinatorial therapeutic strategy applicable to Huntington's disease and other amyloidoses : Développement de nouvelles technologie à haut débit et stratégie thérapeutique combinatoire applicables à la maladie de Huntington et d'autres amyloïdoses.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2015, Université de Strasbourg

Moduler l’agrégation de protéines amyloïdes est thérapeutiquement pertinent (p. ex. la polyneuropathie amyloïde familiale traitée avec le Tafamidis). Cependant, pour de nombreuses amyloïdoses, il n’existe… (more)

Subjects/Keywords: Maladie de Huntington; Polyglutamine; Protéines amyloïdes; Protéines désordonnées intrinsèques; Criblage à haut-débit; Modulateur d'agrégation; Stratégie thérapeutique combinatoire; SynAggreg; Huntington's disease; Polyglutamine diseases; Amyloid; Intrinsically disoredered protein; High-throughput screening; Aggregation modulators; Combinatorial therapeutic strategy; SynAggreg; 615.7; 616.83; 572.8

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APA (6th Edition):

Aviolat, H. (2015). Development of new high-throughput technology and combinatorial therapeutic strategy applicable to Huntington's disease and other amyloidoses : Développement de nouvelles technologie à haut débit et stratégie thérapeutique combinatoire applicables à la maladie de Huntington et d'autres amyloïdoses. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2015STRAJ037

Chicago Manual of Style (16th Edition):

Aviolat, Hubert. “Development of new high-throughput technology and combinatorial therapeutic strategy applicable to Huntington's disease and other amyloidoses : Développement de nouvelles technologie à haut débit et stratégie thérapeutique combinatoire applicables à la maladie de Huntington et d'autres amyloïdoses.” 2015. Doctoral Dissertation, Université de Strasbourg. Accessed August 07, 2020. http://www.theses.fr/2015STRAJ037.

MLA Handbook (7th Edition):

Aviolat, Hubert. “Development of new high-throughput technology and combinatorial therapeutic strategy applicable to Huntington's disease and other amyloidoses : Développement de nouvelles technologie à haut débit et stratégie thérapeutique combinatoire applicables à la maladie de Huntington et d'autres amyloïdoses.” 2015. Web. 07 Aug 2020.

Vancouver:

Aviolat H. Development of new high-throughput technology and combinatorial therapeutic strategy applicable to Huntington's disease and other amyloidoses : Développement de nouvelles technologie à haut débit et stratégie thérapeutique combinatoire applicables à la maladie de Huntington et d'autres amyloïdoses. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2015. [cited 2020 Aug 07]. Available from: http://www.theses.fr/2015STRAJ037.

Council of Science Editors:

Aviolat H. Development of new high-throughput technology and combinatorial therapeutic strategy applicable to Huntington's disease and other amyloidoses : Développement de nouvelles technologie à haut débit et stratégie thérapeutique combinatoire applicables à la maladie de Huntington et d'autres amyloïdoses. [Doctoral Dissertation]. Université de Strasbourg; 2015. Available from: http://www.theses.fr/2015STRAJ037


Brigham Young University

28. Schinn, Song Min. Cell-Free Synthesis of Proteins with Unnatural Amino Acids: Exploring Fitness Landscapes, Engineering Membrane Proteins and Expanding the Genetic Code.

Degree: PhD, 2017, Brigham Young University

 Unnatural amino acids (uAA) expand the structural and functional possibilities of proteins. Numerous previous studies have demonstrated uAA as a powerful tool for protein engineering,… (more)

Subjects/Keywords: Synthetic Biology; cell-free protein synthesis; unnatural amino acid; non-natural amino acid; high throughput screening; linear DNA expression template; membrane proteins; G-protein coupled receptors; codon reassignment; Chemical Engineering

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APA (6th Edition):

Schinn, S. M. (2017). Cell-Free Synthesis of Proteins with Unnatural Amino Acids: Exploring Fitness Landscapes, Engineering Membrane Proteins and Expanding the Genetic Code. (Doctoral Dissertation). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7496&context=etd

Chicago Manual of Style (16th Edition):

Schinn, Song Min. “Cell-Free Synthesis of Proteins with Unnatural Amino Acids: Exploring Fitness Landscapes, Engineering Membrane Proteins and Expanding the Genetic Code.” 2017. Doctoral Dissertation, Brigham Young University. Accessed August 07, 2020. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7496&context=etd.

MLA Handbook (7th Edition):

Schinn, Song Min. “Cell-Free Synthesis of Proteins with Unnatural Amino Acids: Exploring Fitness Landscapes, Engineering Membrane Proteins and Expanding the Genetic Code.” 2017. Web. 07 Aug 2020.

Vancouver:

Schinn SM. Cell-Free Synthesis of Proteins with Unnatural Amino Acids: Exploring Fitness Landscapes, Engineering Membrane Proteins and Expanding the Genetic Code. [Internet] [Doctoral dissertation]. Brigham Young University; 2017. [cited 2020 Aug 07]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7496&context=etd.

Council of Science Editors:

Schinn SM. Cell-Free Synthesis of Proteins with Unnatural Amino Acids: Exploring Fitness Landscapes, Engineering Membrane Proteins and Expanding the Genetic Code. [Doctoral Dissertation]. Brigham Young University; 2017. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7496&context=etd


The Ohio State University

29. Fraley, Brian J. High-Throughput 3-D Cellular Assays Using Destabilized Green Fluorescence Protein.

Degree: MS, Chemical Engineering, 2009, The Ohio State University

  Cell assays for high-throughput screening (HTS) of potential drug candidates are important tools in the process of drug discovery. Most cellular assays are currently… (more)

Subjects/Keywords: Cellular Biology; Chemical Engineering; high-throughput screening; CHO; 3-D cellular assay; optical reporting; green fluorescence protein; destabilized green fluorescence protein; GFP; d4EGFP

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

APA (6th Edition):

Fraley, B. J. (2009). High-Throughput 3-D Cellular Assays Using Destabilized Green Fluorescence Protein. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1250689920

Chicago Manual of Style (16th Edition):

Fraley, Brian J. “High-Throughput 3-D Cellular Assays Using Destabilized Green Fluorescence Protein.” 2009. Masters Thesis, The Ohio State University. Accessed August 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1250689920.

MLA Handbook (7th Edition):

Fraley, Brian J. “High-Throughput 3-D Cellular Assays Using Destabilized Green Fluorescence Protein.” 2009. Web. 07 Aug 2020.

Vancouver:

Fraley BJ. High-Throughput 3-D Cellular Assays Using Destabilized Green Fluorescence Protein. [Internet] [Masters thesis]. The Ohio State University; 2009. [cited 2020 Aug 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1250689920.

Council of Science Editors:

Fraley BJ. High-Throughput 3-D Cellular Assays Using Destabilized Green Fluorescence Protein. [Masters Thesis]. The Ohio State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1250689920


University of Toronto

30. Li, Siyang. Identifying Protein Interactions Amongst DNA Damage Repair Proteins in Yeast.

Degree: 2014, University of Toronto

Mapping protein-protein interactions (PPIs) is crucial for understanding cellular systems. PPIs can be studied with binary or co-complex methods. A major economical binary method is… (more)

Subjects/Keywords: High-throughput; Protein interactions; Yeast two-hybrid; 0307

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

APA (6th Edition):

Li, S. (2014). Identifying Protein Interactions Amongst DNA Damage Repair Proteins in Yeast. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/68505

Chicago Manual of Style (16th Edition):

Li, Siyang. “Identifying Protein Interactions Amongst DNA Damage Repair Proteins in Yeast.” 2014. Masters Thesis, University of Toronto. Accessed August 07, 2020. http://hdl.handle.net/1807/68505.

MLA Handbook (7th Edition):

Li, Siyang. “Identifying Protein Interactions Amongst DNA Damage Repair Proteins in Yeast.” 2014. Web. 07 Aug 2020.

Vancouver:

Li S. Identifying Protein Interactions Amongst DNA Damage Repair Proteins in Yeast. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2020 Aug 07]. Available from: http://hdl.handle.net/1807/68505.

Council of Science Editors:

Li S. Identifying Protein Interactions Amongst DNA Damage Repair Proteins in Yeast. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/68505

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