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You searched for subject:(Protein Engineering). Showing records 91 – 120 of 920 total matches.

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91. Nobrega, Robert P. Early Folding Biases in the Folding Free-Energy Surface of βα-Repeat Proteins: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2014, U of Massachusetts : Med

  Early events in folding can determine if a protein is going to fold, misfold, or aggregate. Understanding these deterministic events is paramount for de… (more)

Subjects/Keywords: Protein Folding; Protein Engineering; Proteins; Biochemistry; Biophysics; Computational Biology; Molecular Biology; Structural Biology

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

APA (6th Edition):

Nobrega, R. P. (2014). Early Folding Biases in the Folding Free-Energy Surface of βα-Repeat Proteins: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/723

Chicago Manual of Style (16th Edition):

Nobrega, Robert P. “Early Folding Biases in the Folding Free-Energy Surface of βα-Repeat Proteins: A Dissertation.” 2014. Doctoral Dissertation, U of Massachusetts : Med. Accessed July 07, 2020. http://escholarship.umassmed.edu/gsbs_diss/723.

MLA Handbook (7th Edition):

Nobrega, Robert P. “Early Folding Biases in the Folding Free-Energy Surface of βα-Repeat Proteins: A Dissertation.” 2014. Web. 07 Jul 2020.

Vancouver:

Nobrega RP. Early Folding Biases in the Folding Free-Energy Surface of βα-Repeat Proteins: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2014. [cited 2020 Jul 07]. Available from: http://escholarship.umassmed.edu/gsbs_diss/723.

Council of Science Editors:

Nobrega RP. Early Folding Biases in the Folding Free-Energy Surface of βα-Repeat Proteins: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2014. Available from: http://escholarship.umassmed.edu/gsbs_diss/723


University of Pennsylvania

92. Wang, Yanxin. Chemical Modification Methods for Protein Misfolding Studies.

Degree: 2015, University of Pennsylvania

Protein misfolding is the basis of various human diseases, including Parkinson’s disease, Alzheimer’s disease and Type 2 diabetes. When a protein misfolds, it adopts the… (more)

Subjects/Keywords: Chemical biology; Parkinson's disease; Protein engineering; Protein semi-synthesis; Synuclein; Thioamide; Biochemistry; Chemistry

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APA (6th Edition):

Wang, Y. (2015). Chemical Modification Methods for Protein Misfolding Studies. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2082

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):

Wang, Yanxin. “Chemical Modification Methods for Protein Misfolding Studies.” 2015. Thesis, University of Pennsylvania. Accessed July 07, 2020. https://repository.upenn.edu/edissertations/2082.

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

MLA Handbook (7th Edition):

Wang, Yanxin. “Chemical Modification Methods for Protein Misfolding Studies.” 2015. Web. 07 Jul 2020.

Vancouver:

Wang Y. Chemical Modification Methods for Protein Misfolding Studies. [Internet] [Thesis]. University of Pennsylvania; 2015. [cited 2020 Jul 07]. Available from: https://repository.upenn.edu/edissertations/2082.

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

Council of Science Editors:

Wang Y. Chemical Modification Methods for Protein Misfolding Studies. [Thesis]. University of Pennsylvania; 2015. Available from: https://repository.upenn.edu/edissertations/2082

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


The Ohio State University

93. Sullivan, Brandon Joseph. Engineering Proteins from Sequence Statistics: Identifying and Understanding the Roles of Conservation and Correlation in Triosephosphate Isomerase.

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

  The structure, function and dynamics of proteins are determined by the physical and chemical properties of their amino acids. Unfortunately, the information encapsulated within… (more)

Subjects/Keywords: Biochemistry; Bioinformatics; Biophysics; Molecular Biology; Protein Engineering; Protein Sequence Statistics; Triosephosphate Isomerase

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

APA (6th Edition):

Sullivan, B. J. (2011). Engineering Proteins from Sequence Statistics: Identifying and Understanding the Roles of Conservation and Correlation in Triosephosphate Isomerase. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1325106135

Chicago Manual of Style (16th Edition):

Sullivan, Brandon Joseph. “Engineering Proteins from Sequence Statistics: Identifying and Understanding the Roles of Conservation and Correlation in Triosephosphate Isomerase.” 2011. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1325106135.

MLA Handbook (7th Edition):

Sullivan, Brandon Joseph. “Engineering Proteins from Sequence Statistics: Identifying and Understanding the Roles of Conservation and Correlation in Triosephosphate Isomerase.” 2011. Web. 07 Jul 2020.

Vancouver:

Sullivan BJ. Engineering Proteins from Sequence Statistics: Identifying and Understanding the Roles of Conservation and Correlation in Triosephosphate Isomerase. [Internet] [Doctoral dissertation]. The Ohio State University; 2011. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1325106135.

Council of Science Editors:

Sullivan BJ. Engineering Proteins from Sequence Statistics: Identifying and Understanding the Roles of Conservation and Correlation in Triosephosphate Isomerase. [Doctoral Dissertation]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1325106135


Cornell University

94. Ludwicki, Morgan Baltz. BROAD-SPECTRUM PROTEOME EDITING WITH AN ENGINEERED BACTERIAL UBIQUITIN LIGASE MIMIC .

Degree: 2019, Cornell University

 Manipulation of the ubiquitin-proteasome pathway to achieve targeted silencing of cellular proteins has emerged as a reliable and customizable strategy for remodeling the mammalian proteome.… (more)

Subjects/Keywords: Chemical engineering; E3 ubiquitin ligase; Ubiquibody; IpaH9.8; Protein knockdown; Targeted protein silencing; Bioengineering

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APA (6th Edition):

Ludwicki, M. B. (2019). BROAD-SPECTRUM PROTEOME EDITING WITH AN ENGINEERED BACTERIAL UBIQUITIN LIGASE MIMIC . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/67803

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):

Ludwicki, Morgan Baltz. “BROAD-SPECTRUM PROTEOME EDITING WITH AN ENGINEERED BACTERIAL UBIQUITIN LIGASE MIMIC .” 2019. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/67803.

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

MLA Handbook (7th Edition):

Ludwicki, Morgan Baltz. “BROAD-SPECTRUM PROTEOME EDITING WITH AN ENGINEERED BACTERIAL UBIQUITIN LIGASE MIMIC .” 2019. Web. 07 Jul 2020.

Vancouver:

Ludwicki MB. BROAD-SPECTRUM PROTEOME EDITING WITH AN ENGINEERED BACTERIAL UBIQUITIN LIGASE MIMIC . [Internet] [Thesis]. Cornell University; 2019. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/67803.

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

Council of Science Editors:

Ludwicki MB. BROAD-SPECTRUM PROTEOME EDITING WITH AN ENGINEERED BACTERIAL UBIQUITIN LIGASE MIMIC . [Thesis]. Cornell University; 2019. Available from: http://hdl.handle.net/1813/67803

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


University of California – Berkeley

95. Metcalf, Kevin James. Engineering heterologous protein secretion for improved production.

Degree: Chemical Engineering, 2016, University of California – Berkeley

 Heterologous protein production in bacteria is often a batch process, where the cells are lysed and the protein of interest is purified from the cellular… (more)

Subjects/Keywords: Chemical engineering; Molecular biology; Biochemistry; Protein production; Protein secretion; Synthetic biology; Type III secretion

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

APA (6th Edition):

Metcalf, K. J. (2016). Engineering heterologous protein secretion for improved production. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/70f4r5n9

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):

Metcalf, Kevin James. “Engineering heterologous protein secretion for improved production.” 2016. Thesis, University of California – Berkeley. Accessed July 07, 2020. http://www.escholarship.org/uc/item/70f4r5n9.

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

MLA Handbook (7th Edition):

Metcalf, Kevin James. “Engineering heterologous protein secretion for improved production.” 2016. Web. 07 Jul 2020.

Vancouver:

Metcalf KJ. Engineering heterologous protein secretion for improved production. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2020 Jul 07]. Available from: http://www.escholarship.org/uc/item/70f4r5n9.

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

Council of Science Editors:

Metcalf KJ. Engineering heterologous protein secretion for improved production. [Thesis]. University of California – Berkeley; 2016. Available from: http://www.escholarship.org/uc/item/70f4r5n9

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

96. Broom, Robert Aron. Computational Design of Protein Structure and Prediction of Ligand Binding.

Degree: 2016, University of Waterloo

 Proteins perform a tremendous array of finely-tuned functions which are not only critical in living organisms, but can be used for industrial and medical purposes.… (more)

Subjects/Keywords: protein engineering; protein design; ligand binding; evolution; symmetry; molecular dynamics; umbrella sampling; metadynamics

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

APA (6th Edition):

Broom, R. A. (2016). Computational Design of Protein Structure and Prediction of Ligand Binding. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/10668

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):

Broom, Robert Aron. “Computational Design of Protein Structure and Prediction of Ligand Binding.” 2016. Thesis, University of Waterloo. Accessed July 07, 2020. http://hdl.handle.net/10012/10668.

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

MLA Handbook (7th Edition):

Broom, Robert Aron. “Computational Design of Protein Structure and Prediction of Ligand Binding.” 2016. Web. 07 Jul 2020.

Vancouver:

Broom RA. Computational Design of Protein Structure and Prediction of Ligand Binding. [Internet] [Thesis]. University of Waterloo; 2016. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/10012/10668.

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

Council of Science Editors:

Broom RA. Computational Design of Protein Structure and Prediction of Ligand Binding. [Thesis]. University of Waterloo; 2016. Available from: http://hdl.handle.net/10012/10668

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


University of Washington

97. Bryan, Cassie Marie. Computational Design of Hyperstable, De Novo Miniproteins Targeting PD-1.

Degree: PhD, 2018, University of Washington

 Computational protein design has recently advanced to a new era with the de novo design of stable proteins targeting native protein ligands. In this dissertation,… (more)

Subjects/Keywords: Computational Design; PD-1; Protein Design; Protein Engineering; Yeast Display; Biochemistry; Bioengineering; Biological chemistry

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

APA (6th Edition):

Bryan, C. M. (2018). Computational Design of Hyperstable, De Novo Miniproteins Targeting PD-1. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/40848

Chicago Manual of Style (16th Edition):

Bryan, Cassie Marie. “Computational Design of Hyperstable, De Novo Miniproteins Targeting PD-1.” 2018. Doctoral Dissertation, University of Washington. Accessed July 07, 2020. http://hdl.handle.net/1773/40848.

MLA Handbook (7th Edition):

Bryan, Cassie Marie. “Computational Design of Hyperstable, De Novo Miniproteins Targeting PD-1.” 2018. Web. 07 Jul 2020.

Vancouver:

Bryan CM. Computational Design of Hyperstable, De Novo Miniproteins Targeting PD-1. [Internet] [Doctoral dissertation]. University of Washington; 2018. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1773/40848.

Council of Science Editors:

Bryan CM. Computational Design of Hyperstable, De Novo Miniproteins Targeting PD-1. [Doctoral Dissertation]. University of Washington; 2018. Available from: http://hdl.handle.net/1773/40848


University of Washington

98. Yu, Shawn. Computational design of interleukin-2 mimetics.

Degree: PhD, 2015, University of Washington

 Interleukin-2 is a cytokine that plays a central role in immune system homeostasis, exerting paradoxical immunostimulatory and immunoregulatory effects based on its interactions with various… (more)

Subjects/Keywords: computational design; interleukin-2; protein design; protein engineering; Rosetta; Biochemistry; Immunology; bioengineering

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APA (6th Edition):

Yu, S. (2015). Computational design of interleukin-2 mimetics. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/33593

Chicago Manual of Style (16th Edition):

Yu, Shawn. “Computational design of interleukin-2 mimetics.” 2015. Doctoral Dissertation, University of Washington. Accessed July 07, 2020. http://hdl.handle.net/1773/33593.

MLA Handbook (7th Edition):

Yu, Shawn. “Computational design of interleukin-2 mimetics.” 2015. Web. 07 Jul 2020.

Vancouver:

Yu S. Computational design of interleukin-2 mimetics. [Internet] [Doctoral dissertation]. University of Washington; 2015. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1773/33593.

Council of Science Editors:

Yu S. Computational design of interleukin-2 mimetics. [Doctoral Dissertation]. University of Washington; 2015. Available from: http://hdl.handle.net/1773/33593


University of Washington

99. Haydon, Ian. De novo protein fusions as platforms for enzyme design.

Degree: 2019, University of Washington

 Control over enzymatic catalysis is a central goal of biotechnology. Recent advances in computational protein design are beginning to allow for the de novo creation… (more)

Subjects/Keywords: computational biology; enzymes; protein design; protein engineering; Biochemistry; Bioengineering; Biophysics; Biological chemistry

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

APA (6th Edition):

Haydon, I. (2019). De novo protein fusions as platforms for enzyme design. (Thesis). University of Washington. Retrieved from http://hdl.handle.net/1773/43305

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):

Haydon, Ian. “De novo protein fusions as platforms for enzyme design.” 2019. Thesis, University of Washington. Accessed July 07, 2020. http://hdl.handle.net/1773/43305.

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

MLA Handbook (7th Edition):

Haydon, Ian. “De novo protein fusions as platforms for enzyme design.” 2019. Web. 07 Jul 2020.

Vancouver:

Haydon I. De novo protein fusions as platforms for enzyme design. [Internet] [Thesis]. University of Washington; 2019. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1773/43305.

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

Council of Science Editors:

Haydon I. De novo protein fusions as platforms for enzyme design. [Thesis]. University of Washington; 2019. Available from: http://hdl.handle.net/1773/43305

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


Drexel University

100. Liu, Yichuan. Functional signatures in protein-protein interactions and their impact on signaling pathways.

Degree: 2010, Drexel University

Protein-protein interactions (PPIs) are the most fundamental biological processes at the molecular level. PPIs have been proved to be involved in pathologic mechanisms of many… (more)

Subjects/Keywords: Biomedical engineering; Bioinformatics; Protein-protein interactions

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APA (6th Edition):

Liu, Y. (2010). Functional signatures in protein-protein interactions and their impact on signaling pathways. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/3257

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):

Liu, Yichuan. “Functional signatures in protein-protein interactions and their impact on signaling pathways.” 2010. Thesis, Drexel University. Accessed July 07, 2020. http://hdl.handle.net/1860/3257.

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

MLA Handbook (7th Edition):

Liu, Yichuan. “Functional signatures in protein-protein interactions and their impact on signaling pathways.” 2010. Web. 07 Jul 2020.

Vancouver:

Liu Y. Functional signatures in protein-protein interactions and their impact on signaling pathways. [Internet] [Thesis]. Drexel University; 2010. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1860/3257.

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

Council of Science Editors:

Liu Y. Functional signatures in protein-protein interactions and their impact on signaling pathways. [Thesis]. Drexel University; 2010. Available from: http://hdl.handle.net/1860/3257

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


University of Kentucky

101. Zhan, Ruiqian. Diffusion-Mediated Deposition of Proteins.

Degree: 2016, University of Kentucky

 Gradients of proteins play a prominent role in many biological processes, from development of multicellular organisms to chemical signaling in the immune system. Deposition of… (more)

Subjects/Keywords: Gradient of Protein; Deposition of Protein; Diffusion; 3D PEG; Biomedical Engineering and Bioengineering; Chemical Engineering; Mechanical Engineering

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APA (6th Edition):

Zhan, R. (2016). Diffusion-Mediated Deposition of Proteins. (Masters Thesis). University of Kentucky. Retrieved from http://uknowledge.uky.edu/me_etds/81

Chicago Manual of Style (16th Edition):

Zhan, Ruiqian. “Diffusion-Mediated Deposition of Proteins.” 2016. Masters Thesis, University of Kentucky. Accessed July 07, 2020. http://uknowledge.uky.edu/me_etds/81.

MLA Handbook (7th Edition):

Zhan, Ruiqian. “Diffusion-Mediated Deposition of Proteins.” 2016. Web. 07 Jul 2020.

Vancouver:

Zhan R. Diffusion-Mediated Deposition of Proteins. [Internet] [Masters thesis]. University of Kentucky; 2016. [cited 2020 Jul 07]. Available from: http://uknowledge.uky.edu/me_etds/81.

Council of Science Editors:

Zhan R. Diffusion-Mediated Deposition of Proteins. [Masters Thesis]. University of Kentucky; 2016. Available from: http://uknowledge.uky.edu/me_etds/81


The Ohio State University

102. Stimple, Samuel Douglas. Recent Advances in Developing Molecular Biotechnology Tools for Metabolic Engineering and Recombinant Protein Purification.

Degree: PhD, Chemical Engineering, 2018, The Ohio State University

 The development of platform technologies can dramatically impact the speed and ease with which new biological processes/products can be optimized and brought to market. Platform… (more)

Subjects/Keywords: Chemical Engineering; protein purification, intein, protein engineering, self-cleaving affinity tag, sRNAs, metabolic engineering, gene regulation, noncoding sRNA, synthetic biology

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APA (6th Edition):

Stimple, S. D. (2018). Recent Advances in Developing Molecular Biotechnology Tools for Metabolic Engineering and Recombinant Protein Purification. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1514494485801145

Chicago Manual of Style (16th Edition):

Stimple, Samuel Douglas. “Recent Advances in Developing Molecular Biotechnology Tools for Metabolic Engineering and Recombinant Protein Purification.” 2018. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1514494485801145.

MLA Handbook (7th Edition):

Stimple, Samuel Douglas. “Recent Advances in Developing Molecular Biotechnology Tools for Metabolic Engineering and Recombinant Protein Purification.” 2018. Web. 07 Jul 2020.

Vancouver:

Stimple SD. Recent Advances in Developing Molecular Biotechnology Tools for Metabolic Engineering and Recombinant Protein Purification. [Internet] [Doctoral dissertation]. The Ohio State University; 2018. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1514494485801145.

Council of Science Editors:

Stimple SD. Recent Advances in Developing Molecular Biotechnology Tools for Metabolic Engineering and Recombinant Protein Purification. [Doctoral Dissertation]. The Ohio State University; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1514494485801145


University of California – Berkeley

103. Dana, Craig Matthew. Cel7A Engineering and Expression.

Degree: Chemical Engineering, 2013, University of California – Berkeley

 Renewable fuels produced from biomass-derived sugars are receiving increasing attention. Lignocellulose-degrading enzymes derived from fungi are attractive for saccharification of biomass because they can be… (more)

Subjects/Keywords: Chemical engineering; CBHI; Cel7A; cellulase; protein engineering; recombinant expression; saccharomyces cerevisiae

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APA (6th Edition):

Dana, C. M. (2013). Cel7A Engineering and Expression. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/3sb6n3n5

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):

Dana, Craig Matthew. “Cel7A Engineering and Expression.” 2013. Thesis, University of California – Berkeley. Accessed July 07, 2020. http://www.escholarship.org/uc/item/3sb6n3n5.

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

MLA Handbook (7th Edition):

Dana, Craig Matthew. “Cel7A Engineering and Expression.” 2013. Web. 07 Jul 2020.

Vancouver:

Dana CM. Cel7A Engineering and Expression. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2020 Jul 07]. Available from: http://www.escholarship.org/uc/item/3sb6n3n5.

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

Council of Science Editors:

Dana CM. Cel7A Engineering and Expression. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/3sb6n3n5

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


University of California – Berkeley

104. Strobel, Kathryn Lynn. Understanding and Engineering Cellulase Binding to Biomass Components.

Degree: Chemical Engineering, 2015, University of California – Berkeley

 Lignocellulosic biomass is an abundant, low-cost resource for the renewable production of fuels and chemicals. To unlock the potential of lignocellulosic biomass, the cellulose must… (more)

Subjects/Keywords: Chemical engineering; Biochemistry; Biofuels; Cellulase; Lignin; Protease; Protein engineering

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APA (6th Edition):

Strobel, K. L. (2015). Understanding and Engineering Cellulase Binding to Biomass Components. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/0tw1f2tz

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):

Strobel, Kathryn Lynn. “Understanding and Engineering Cellulase Binding to Biomass Components.” 2015. Thesis, University of California – Berkeley. Accessed July 07, 2020. http://www.escholarship.org/uc/item/0tw1f2tz.

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

MLA Handbook (7th Edition):

Strobel, Kathryn Lynn. “Understanding and Engineering Cellulase Binding to Biomass Components.” 2015. Web. 07 Jul 2020.

Vancouver:

Strobel KL. Understanding and Engineering Cellulase Binding to Biomass Components. [Internet] [Thesis]. University of California – Berkeley; 2015. [cited 2020 Jul 07]. Available from: http://www.escholarship.org/uc/item/0tw1f2tz.

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

Council of Science Editors:

Strobel KL. Understanding and Engineering Cellulase Binding to Biomass Components. [Thesis]. University of California – Berkeley; 2015. Available from: http://www.escholarship.org/uc/item/0tw1f2tz

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


Boston University

105. Dehghani, Bijan. Development of an elastic sealant for surgical applications.

Degree: MS, Medical Sciences, 2015, Boston University

 The need to close wounds and prevent air/liquid leakage is commonly faced in surgical operations. It is a necessary step required for proper post-operative tissue… (more)

Subjects/Keywords: Biomedical engineering; Biomaterials; Elastin; Human recombinant protein; Sealant; Surgery; Tissue engineering

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APA (6th Edition):

Dehghani, B. (2015). Development of an elastic sealant for surgical applications. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/16139

Chicago Manual of Style (16th Edition):

Dehghani, Bijan. “Development of an elastic sealant for surgical applications.” 2015. Masters Thesis, Boston University. Accessed July 07, 2020. http://hdl.handle.net/2144/16139.

MLA Handbook (7th Edition):

Dehghani, Bijan. “Development of an elastic sealant for surgical applications.” 2015. Web. 07 Jul 2020.

Vancouver:

Dehghani B. Development of an elastic sealant for surgical applications. [Internet] [Masters thesis]. Boston University; 2015. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/2144/16139.

Council of Science Editors:

Dehghani B. Development of an elastic sealant for surgical applications. [Masters Thesis]. Boston University; 2015. Available from: http://hdl.handle.net/2144/16139


University of Colorado

106. Nordwald, Erik Michael. Engineering ionic liquid tolerant enzymes.

Degree: PhD, Chemical & Biochemical Engineering, 2015, University of Colorado

  As media for biocatalysis, imidazolium based ionic liquids (ILs) have many applications, including improving enzyme refolding, selectivity, and replacing organic solvents as either the… (more)

Subjects/Keywords: Biocatalysis; Ionic Liquids; Protein Engineering; Biochemistry; Chemical Engineering

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APA (6th Edition):

Nordwald, E. M. (2015). Engineering ionic liquid tolerant enzymes. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/89

Chicago Manual of Style (16th Edition):

Nordwald, Erik Michael. “Engineering ionic liquid tolerant enzymes.” 2015. Doctoral Dissertation, University of Colorado. Accessed July 07, 2020. https://scholar.colorado.edu/chbe_gradetds/89.

MLA Handbook (7th Edition):

Nordwald, Erik Michael. “Engineering ionic liquid tolerant enzymes.” 2015. Web. 07 Jul 2020.

Vancouver:

Nordwald EM. Engineering ionic liquid tolerant enzymes. [Internet] [Doctoral dissertation]. University of Colorado; 2015. [cited 2020 Jul 07]. Available from: https://scholar.colorado.edu/chbe_gradetds/89.

Council of Science Editors:

Nordwald EM. Engineering ionic liquid tolerant enzymes. [Doctoral Dissertation]. University of Colorado; 2015. Available from: https://scholar.colorado.edu/chbe_gradetds/89


KTH

107. 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 July 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 Jul 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 Jul 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 Washington

108. Liu, Luman. Cyclic Stiffness Photomodulation of Cell-Laden Protein-Polymer Hydrogels.

Degree: 2017, University of Washington

 Although mechanical signals presented by the extracellular matrix are known to regulate many essential cell functions, the specific effects of these interactions, particularly in response… (more)

Subjects/Keywords: Cell culture; Hydrogel; Luciferase; Peptide; Protein; Stiffness; Chemical engineering; Chemical engineering

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

APA (6th Edition):

Liu, L. (2017). Cyclic Stiffness Photomodulation of Cell-Laden Protein-Polymer Hydrogels. (Thesis). University of Washington. Retrieved from http://hdl.handle.net/1773/40508

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):

Liu, Luman. “Cyclic Stiffness Photomodulation of Cell-Laden Protein-Polymer Hydrogels.” 2017. Thesis, University of Washington. Accessed July 07, 2020. http://hdl.handle.net/1773/40508.

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

MLA Handbook (7th Edition):

Liu, Luman. “Cyclic Stiffness Photomodulation of Cell-Laden Protein-Polymer Hydrogels.” 2017. Web. 07 Jul 2020.

Vancouver:

Liu L. Cyclic Stiffness Photomodulation of Cell-Laden Protein-Polymer Hydrogels. [Internet] [Thesis]. University of Washington; 2017. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1773/40508.

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

Council of Science Editors:

Liu L. Cyclic Stiffness Photomodulation of Cell-Laden Protein-Polymer Hydrogels. [Thesis]. University of Washington; 2017. Available from: http://hdl.handle.net/1773/40508

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


University of Washington

109. Tung, Hsin-Ju. Accelerating protein unfolding simulations: Effect of ionic liquids on villin headpiece unfolding time.

Degree: 2016, University of Washington

 We demonstrate an approach to accelerate protein unfolding simulation using the metadynamics (MetaD) method, and the new rate calculation method “infrequent metadynamics”. The accelerated simulation… (more)

Subjects/Keywords: Molecular dynamics; Protein unfold; Chemical engineering; Biochemistry; chemical engineering

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APA (6th Edition):

Tung, H. (2016). Accelerating protein unfolding simulations: Effect of ionic liquids on villin headpiece unfolding time. (Thesis). University of Washington. Retrieved from http://hdl.handle.net/1773/35547

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):

Tung, Hsin-Ju. “Accelerating protein unfolding simulations: Effect of ionic liquids on villin headpiece unfolding time.” 2016. Thesis, University of Washington. Accessed July 07, 2020. http://hdl.handle.net/1773/35547.

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

MLA Handbook (7th Edition):

Tung, Hsin-Ju. “Accelerating protein unfolding simulations: Effect of ionic liquids on villin headpiece unfolding time.” 2016. Web. 07 Jul 2020.

Vancouver:

Tung H. Accelerating protein unfolding simulations: Effect of ionic liquids on villin headpiece unfolding time. [Internet] [Thesis]. University of Washington; 2016. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1773/35547.

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

Council of Science Editors:

Tung H. Accelerating protein unfolding simulations: Effect of ionic liquids on villin headpiece unfolding time. [Thesis]. University of Washington; 2016. Available from: http://hdl.handle.net/1773/35547

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


University of Washington

110. Shao, Qing. Understanding Properties of Zwitterionic Materials from Their Molecular Structures.

Degree: PhD, 2014, University of Washington

 Materials that resist nonspecific protein adsorption in complex media are important for many biological and chemical applications, such as surface coatings of biosensors, marine coatings,… (more)

Subjects/Keywords: hydration; molecular simulation; nonspecific protein adsorption; zwitterion; Chemical engineering; chemical engineering

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APA (6th Edition):

Shao, Q. (2014). Understanding Properties of Zwitterionic Materials from Their Molecular Structures. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/25365

Chicago Manual of Style (16th Edition):

Shao, Qing. “Understanding Properties of Zwitterionic Materials from Their Molecular Structures.” 2014. Doctoral Dissertation, University of Washington. Accessed July 07, 2020. http://hdl.handle.net/1773/25365.

MLA Handbook (7th Edition):

Shao, Qing. “Understanding Properties of Zwitterionic Materials from Their Molecular Structures.” 2014. Web. 07 Jul 2020.

Vancouver:

Shao Q. Understanding Properties of Zwitterionic Materials from Their Molecular Structures. [Internet] [Doctoral dissertation]. University of Washington; 2014. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1773/25365.

Council of Science Editors:

Shao Q. Understanding Properties of Zwitterionic Materials from Their Molecular Structures. [Doctoral Dissertation]. University of Washington; 2014. Available from: http://hdl.handle.net/1773/25365


University of Minnesota

111. McClintock, Maria. Synthetic Biology Approach to New Sustainable Materials.

Degree: PhD, Chemical Engineering, 2018, University of Minnesota

 Rapid industrialization and an abundance of cheap petroleum fueled the production and development of a great variety of synthetic polymers in the twentieth century. Over… (more)

Subjects/Keywords: Lignocellulosic feedstocks; Metabolic engineering; Protein engineering; Sustainable polymers

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APA (6th Edition):

McClintock, M. (2018). Synthetic Biology Approach to New Sustainable Materials. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/213128

Chicago Manual of Style (16th Edition):

McClintock, Maria. “Synthetic Biology Approach to New Sustainable Materials.” 2018. Doctoral Dissertation, University of Minnesota. Accessed July 07, 2020. http://hdl.handle.net/11299/213128.

MLA Handbook (7th Edition):

McClintock, Maria. “Synthetic Biology Approach to New Sustainable Materials.” 2018. Web. 07 Jul 2020.

Vancouver:

McClintock M. Synthetic Biology Approach to New Sustainable Materials. [Internet] [Doctoral dissertation]. University of Minnesota; 2018. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/11299/213128.

Council of Science Editors:

McClintock M. Synthetic Biology Approach to New Sustainable Materials. [Doctoral Dissertation]. University of Minnesota; 2018. Available from: http://hdl.handle.net/11299/213128


Georgia Tech

112. Hyland, Kelly Elise. Immobilization of adhesive protein domains in PEG hydrogels.

Degree: MS, Materials Science and Engineering, 2018, Georgia Tech

 The fundamental goal of biomaterials design for regenerative medicine is to promote the restoration of functional tissue. In wound healing research, one strategy is to… (more)

Subjects/Keywords: Protein engineering; Hydrogel; Tissue engineering; Wound healing; Regenerative medicine

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APA (6th Edition):

Hyland, K. E. (2018). Immobilization of adhesive protein domains in PEG hydrogels. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/61656

Chicago Manual of Style (16th Edition):

Hyland, Kelly Elise. “Immobilization of adhesive protein domains in PEG hydrogels.” 2018. Masters Thesis, Georgia Tech. Accessed July 07, 2020. http://hdl.handle.net/1853/61656.

MLA Handbook (7th Edition):

Hyland, Kelly Elise. “Immobilization of adhesive protein domains in PEG hydrogels.” 2018. Web. 07 Jul 2020.

Vancouver:

Hyland KE. Immobilization of adhesive protein domains in PEG hydrogels. [Internet] [Masters thesis]. Georgia Tech; 2018. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1853/61656.

Council of Science Editors:

Hyland KE. Immobilization of adhesive protein domains in PEG hydrogels. [Masters Thesis]. Georgia Tech; 2018. Available from: http://hdl.handle.net/1853/61656


Arizona State University

113. Tekel, Stefan. Engineering and Delivery of Synthetic Chromatin Effectors.

Degree: Biological Design, 2019, Arizona State University

 Synthetic manipulation of chromatin dynamics has applications for medicine, agriculture, and biotechnology. However, progress in this area requires the identification of design rules for engineering(more)

Subjects/Keywords: Bioengineering; Chromatin Engineering; Epigenetics; PcTF; Protein Engineering; Synthetic Biology

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APA (6th Edition):

Tekel, S. (2019). Engineering and Delivery of Synthetic Chromatin Effectors. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/53486

Chicago Manual of Style (16th Edition):

Tekel, Stefan. “Engineering and Delivery of Synthetic Chromatin Effectors.” 2019. Doctoral Dissertation, Arizona State University. Accessed July 07, 2020. http://repository.asu.edu/items/53486.

MLA Handbook (7th Edition):

Tekel, Stefan. “Engineering and Delivery of Synthetic Chromatin Effectors.” 2019. Web. 07 Jul 2020.

Vancouver:

Tekel S. Engineering and Delivery of Synthetic Chromatin Effectors. [Internet] [Doctoral dissertation]. Arizona State University; 2019. [cited 2020 Jul 07]. Available from: http://repository.asu.edu/items/53486.

Council of Science Editors:

Tekel S. Engineering and Delivery of Synthetic Chromatin Effectors. [Doctoral Dissertation]. Arizona State University; 2019. Available from: http://repository.asu.edu/items/53486


Indian Institute of Science

114. Sharma, Likhesh. Modulation of Protein Stability and Function by Cysteine Mutations and Signal Peptides.

Degree: 2016, Indian Institute of Science

 Chapter 1gives a general introduction to the CXXC motif found in natural proteins. It then reviews the studies where disulphides were engineered in various proteins.… (more)

Subjects/Keywords: Engineering Disulphide Bonds; Signal Peptides; Maltose Binding Protein; Protein Stability; Protein Export; E.coli Thioredoxin; Maltose-binding Protein (MBP); Cysteine Mutation; Molecular Biophysics

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APA (6th Edition):

Sharma, L. (2016). Modulation of Protein Stability and Function by Cysteine Mutations and Signal Peptides. (Thesis). Indian Institute of Science. Retrieved from http://etd.iisc.ernet.in/2005/3746 ; http://etd.iisc.ernet.in/abstracts/4617/G28410-Abs.pdf

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):

Sharma, Likhesh. “Modulation of Protein Stability and Function by Cysteine Mutations and Signal Peptides.” 2016. Thesis, Indian Institute of Science. Accessed July 07, 2020. http://etd.iisc.ernet.in/2005/3746 ; http://etd.iisc.ernet.in/abstracts/4617/G28410-Abs.pdf.

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

MLA Handbook (7th Edition):

Sharma, Likhesh. “Modulation of Protein Stability and Function by Cysteine Mutations and Signal Peptides.” 2016. Web. 07 Jul 2020.

Vancouver:

Sharma L. Modulation of Protein Stability and Function by Cysteine Mutations and Signal Peptides. [Internet] [Thesis]. Indian Institute of Science; 2016. [cited 2020 Jul 07]. Available from: http://etd.iisc.ernet.in/2005/3746 ; http://etd.iisc.ernet.in/abstracts/4617/G28410-Abs.pdf.

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

Council of Science Editors:

Sharma L. Modulation of Protein Stability and Function by Cysteine Mutations and Signal Peptides. [Thesis]. Indian Institute of Science; 2016. Available from: http://etd.iisc.ernet.in/2005/3746 ; http://etd.iisc.ernet.in/abstracts/4617/G28410-Abs.pdf

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


Université Paris-Sud – Paris XI

115. Chevrel, Anne. Ingénierie d’une ossature à motifs structuraux répétés par évolution dirigée : développements et applications d’un nouvel outil de reconnaissance moléculaire : Engineering of a repeat protein scaffold by directed evolution : Developments and Applications of a new tool for molecular recognition.

Degree: Docteur es, Ingénierie des protéines, 2014, Université Paris-Sud – Paris XI

 Les immunoglobulines ne sont pas les seules protéines capables de reconnaissance spécifique. D’autres systèmes d’immunité adaptative existent et beaucoup d’autres protéines peuvent aussi générer des… (more)

Subjects/Keywords: AlphaRep; Ossature protéique; Évolution dirigée; Ingénierie des protéines; Interaction protéine-protéine; Outil de reconnaissance moléculaire; AlphaRep; Protein scaffold; Directed evolution; Protein engineering; Protein-protein interaction; Tool for molecular recognition

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APA (6th Edition):

Chevrel, A. (2014). Ingénierie d’une ossature à motifs structuraux répétés par évolution dirigée : développements et applications d’un nouvel outil de reconnaissance moléculaire : Engineering of a repeat protein scaffold by directed evolution : Developments and Applications of a new tool for molecular recognition. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2014PA114842

Chicago Manual of Style (16th Edition):

Chevrel, Anne. “Ingénierie d’une ossature à motifs structuraux répétés par évolution dirigée : développements et applications d’un nouvel outil de reconnaissance moléculaire : Engineering of a repeat protein scaffold by directed evolution : Developments and Applications of a new tool for molecular recognition.” 2014. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed July 07, 2020. http://www.theses.fr/2014PA114842.

MLA Handbook (7th Edition):

Chevrel, Anne. “Ingénierie d’une ossature à motifs structuraux répétés par évolution dirigée : développements et applications d’un nouvel outil de reconnaissance moléculaire : Engineering of a repeat protein scaffold by directed evolution : Developments and Applications of a new tool for molecular recognition.” 2014. Web. 07 Jul 2020.

Vancouver:

Chevrel A. Ingénierie d’une ossature à motifs structuraux répétés par évolution dirigée : développements et applications d’un nouvel outil de reconnaissance moléculaire : Engineering of a repeat protein scaffold by directed evolution : Developments and Applications of a new tool for molecular recognition. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2014. [cited 2020 Jul 07]. Available from: http://www.theses.fr/2014PA114842.

Council of Science Editors:

Chevrel A. Ingénierie d’une ossature à motifs structuraux répétés par évolution dirigée : développements et applications d’un nouvel outil de reconnaissance moléculaire : Engineering of a repeat protein scaffold by directed evolution : Developments and Applications of a new tool for molecular recognition. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2014. Available from: http://www.theses.fr/2014PA114842

116. Glidden, Michael D., II. Single-chain insulin analogs as ultra-stable therapeutics and as models of protein (mis)folding: stability, structure, dynamics, and function of novel analogs.

Degree: PhD, Physiology and Biophysics, 2018, Case Western Reserve University School of Graduate Studies

 Single-chain insulin (SCI) analogs have long provided a valuable model for structure-function studies of insulin. Recently, a biologically active SCI containing a six-residue connecting (C)… (more)

Subjects/Keywords: Biophysics; Biochemistry; single-chain insulin analog; hormone; diabetes mellitus; protein engineering; protein stability; protein structure and folding; protein dynamics; nuclear magnetic resonance; single-chain insulin pharmacology

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APA (6th Edition):

Glidden, Michael D., I. (2018). Single-chain insulin analogs as ultra-stable therapeutics and as models of protein (mis)folding: stability, structure, dynamics, and function of novel analogs. (Doctoral Dissertation). Case Western Reserve University School of Graduate Studies. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1522270994798884

Chicago Manual of Style (16th Edition):

Glidden, Michael D., II. “Single-chain insulin analogs as ultra-stable therapeutics and as models of protein (mis)folding: stability, structure, dynamics, and function of novel analogs.” 2018. Doctoral Dissertation, Case Western Reserve University School of Graduate Studies. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1522270994798884.

MLA Handbook (7th Edition):

Glidden, Michael D., II. “Single-chain insulin analogs as ultra-stable therapeutics and as models of protein (mis)folding: stability, structure, dynamics, and function of novel analogs.” 2018. Web. 07 Jul 2020.

Vancouver:

Glidden, Michael D. I. Single-chain insulin analogs as ultra-stable therapeutics and as models of protein (mis)folding: stability, structure, dynamics, and function of novel analogs. [Internet] [Doctoral dissertation]. Case Western Reserve University School of Graduate Studies; 2018. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1522270994798884.

Council of Science Editors:

Glidden, Michael D. I. Single-chain insulin analogs as ultra-stable therapeutics and as models of protein (mis)folding: stability, structure, dynamics, and function of novel analogs. [Doctoral Dissertation]. Case Western Reserve University School of Graduate Studies; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1522270994798884


UCLA

117. Hinkle, Trent. Designing Protein Energy Landscapes With Coarse-Grained Sequence-Energy Mappings.

Degree: Chemical Engineering, 2017, UCLA

 We develop and implement a brand new method for protein design. Our design method utilizes advances in protein energy scoring, Markov state modeling, machine learning,… (more)

Subjects/Keywords: Biochemistry; Applied mathematics; Chemical engineering; Computational Biology; Computational Protein Design; Machine Learning; Markov State Model; Mean Field Energy Model; Protein Engineering

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APA (6th Edition):

Hinkle, T. (2017). Designing Protein Energy Landscapes With Coarse-Grained Sequence-Energy Mappings. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/7tm0g6xf

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):

Hinkle, Trent. “Designing Protein Energy Landscapes With Coarse-Grained Sequence-Energy Mappings.” 2017. Thesis, UCLA. Accessed July 07, 2020. http://www.escholarship.org/uc/item/7tm0g6xf.

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

MLA Handbook (7th Edition):

Hinkle, Trent. “Designing Protein Energy Landscapes With Coarse-Grained Sequence-Energy Mappings.” 2017. Web. 07 Jul 2020.

Vancouver:

Hinkle T. Designing Protein Energy Landscapes With Coarse-Grained Sequence-Energy Mappings. [Internet] [Thesis]. UCLA; 2017. [cited 2020 Jul 07]. Available from: http://www.escholarship.org/uc/item/7tm0g6xf.

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

Council of Science Editors:

Hinkle T. Designing Protein Energy Landscapes With Coarse-Grained Sequence-Energy Mappings. [Thesis]. UCLA; 2017. Available from: http://www.escholarship.org/uc/item/7tm0g6xf

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


University of California – Berkeley

118. Slininger, Marilyn F. Development of protein organelles for tunable metabolite diffusion and sequestration of multi-enzyme pathways.

Degree: Chemical Engineering, 2017, University of California – Berkeley

 The use of bacterial production could improve commercial feasibility for biochemicals such as pharmaceuticals and natural products. However, many non-native reactions in bacterial hosts have… (more)

Subjects/Keywords: Chemical engineering; Molecular biology; Biochemistry; 1,2-propanediol utilization; Bacterial Microcompartment; Metabolic engineering; Metabolosome; Protein pore diffusion; Protein scaffold

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APA (6th Edition):

Slininger, M. F. (2017). Development of protein organelles for tunable metabolite diffusion and sequestration of multi-enzyme pathways. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/8w29d1cs

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):

Slininger, Marilyn F. “Development of protein organelles for tunable metabolite diffusion and sequestration of multi-enzyme pathways.” 2017. Thesis, University of California – Berkeley. Accessed July 07, 2020. http://www.escholarship.org/uc/item/8w29d1cs.

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

MLA Handbook (7th Edition):

Slininger, Marilyn F. “Development of protein organelles for tunable metabolite diffusion and sequestration of multi-enzyme pathways.” 2017. Web. 07 Jul 2020.

Vancouver:

Slininger MF. Development of protein organelles for tunable metabolite diffusion and sequestration of multi-enzyme pathways. [Internet] [Thesis]. University of California – Berkeley; 2017. [cited 2020 Jul 07]. Available from: http://www.escholarship.org/uc/item/8w29d1cs.

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

Council of Science Editors:

Slininger MF. Development of protein organelles for tunable metabolite diffusion and sequestration of multi-enzyme pathways. [Thesis]. University of California – Berkeley; 2017. Available from: http://www.escholarship.org/uc/item/8w29d1cs

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


Lehigh University

119. Bhattacharya, Apratim. Protein folding and Protein-Protein interactions in a Cell-like environment.

Degree: PhD, Chemical Engineering, 2014, Lehigh University

 The cellular environment is highly crowded owing to the presence of several kinds of macromolecules such as lipids, sugars, nucleic acids, and proteins, along with… (more)

Subjects/Keywords: Computational Biophysics; Confinement; Enhanced Sampling; Molecular Dynamics Simulations; Protein-protein interactions; Statistical Thermodynamics; Chemical Engineering; Engineering

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APA (6th Edition):

Bhattacharya, A. (2014). Protein folding and Protein-Protein interactions in a Cell-like environment. (Doctoral Dissertation). Lehigh University. Retrieved from https://preserve.lehigh.edu/etd/1427

Chicago Manual of Style (16th Edition):

Bhattacharya, Apratim. “Protein folding and Protein-Protein interactions in a Cell-like environment.” 2014. Doctoral Dissertation, Lehigh University. Accessed July 07, 2020. https://preserve.lehigh.edu/etd/1427.

MLA Handbook (7th Edition):

Bhattacharya, Apratim. “Protein folding and Protein-Protein interactions in a Cell-like environment.” 2014. Web. 07 Jul 2020.

Vancouver:

Bhattacharya A. Protein folding and Protein-Protein interactions in a Cell-like environment. [Internet] [Doctoral dissertation]. Lehigh University; 2014. [cited 2020 Jul 07]. Available from: https://preserve.lehigh.edu/etd/1427.

Council of Science Editors:

Bhattacharya A. Protein folding and Protein-Protein interactions in a Cell-like environment. [Doctoral Dissertation]. Lehigh University; 2014. Available from: https://preserve.lehigh.edu/etd/1427


University of Dayton

120. Nelson, William Forrester. An Investigation into the Use of Mussel Adhesive Proteins as Temporary Corrosion Inhibitors for HY80 Steel.

Degree: MS(M.S.), Chemical Engineering, 2014, University of Dayton

 Several proteins found in the adhesive system of the common blue mussel <i>Mytilus edulis</i> have chemical properties which might enable them to inhibit the flash… (more)

Subjects/Keywords: Materials Science; Biochemistry; Engineering; Naval Engineering; flash rust; corrosion inhibitor; flash rust inhibitor; mussel protein; mussel adhesive protein; MAP; MeFP

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

APA (6th Edition):

Nelson, W. F. (2014). An Investigation into the Use of Mussel Adhesive Proteins as Temporary Corrosion Inhibitors for HY80 Steel. (Masters Thesis). University of Dayton. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=dayton1417774059

Chicago Manual of Style (16th Edition):

Nelson, William Forrester. “An Investigation into the Use of Mussel Adhesive Proteins as Temporary Corrosion Inhibitors for HY80 Steel.” 2014. Masters Thesis, University of Dayton. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=dayton1417774059.

MLA Handbook (7th Edition):

Nelson, William Forrester. “An Investigation into the Use of Mussel Adhesive Proteins as Temporary Corrosion Inhibitors for HY80 Steel.” 2014. Web. 07 Jul 2020.

Vancouver:

Nelson WF. An Investigation into the Use of Mussel Adhesive Proteins as Temporary Corrosion Inhibitors for HY80 Steel. [Internet] [Masters thesis]. University of Dayton; 2014. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=dayton1417774059.

Council of Science Editors:

Nelson WF. An Investigation into the Use of Mussel Adhesive Proteins as Temporary Corrosion Inhibitors for HY80 Steel. [Masters Thesis]. University of Dayton; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=dayton1417774059

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