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You searched for +publisher:"Cornell University" +contributor:("Delisa,Matthew"). Showing records 1 – 30 of 39 total matches.

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Cornell University

1. Kashyap, Kritika. MODELING BIOLOGICAL SYSTEMS WITH CYBERNETIC CONTROL LAWS AND STEADY STATE FLUX DISTRIBUTIONS.

Degree: M.S., Chemical Engineering, Chemical Engineering, 2019, Cornell University

 Metabolism is a process by which organisms extract energy from its environment to power itself. The interplay between cellular environment, nutrients present and the chemical… (more)

Subjects/Keywords: Cybernetic Modeling; Flux Balance Analysis; Markov Chain Monte Carlo; Metabolic Engineering; Modeling Cell Growth for E. coli and CHO cells; Steady State Flux Analysis

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APA (6th Edition):

Kashyap, K. (2019). MODELING BIOLOGICAL SYSTEMS WITH CYBERNETIC CONTROL LAWS AND STEADY STATE FLUX DISTRIBUTIONS. (Masters Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/70034

Chicago Manual of Style (16th Edition):

Kashyap, Kritika. “MODELING BIOLOGICAL SYSTEMS WITH CYBERNETIC CONTROL LAWS AND STEADY STATE FLUX DISTRIBUTIONS.” 2019. Masters Thesis, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/70034.

MLA Handbook (7th Edition):

Kashyap, Kritika. “MODELING BIOLOGICAL SYSTEMS WITH CYBERNETIC CONTROL LAWS AND STEADY STATE FLUX DISTRIBUTIONS.” 2019. Web. 07 May 2021.

Vancouver:

Kashyap K. MODELING BIOLOGICAL SYSTEMS WITH CYBERNETIC CONTROL LAWS AND STEADY STATE FLUX DISTRIBUTIONS. [Internet] [Masters thesis]. Cornell University; 2019. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/70034.

Council of Science Editors:

Kashyap K. MODELING BIOLOGICAL SYSTEMS WITH CYBERNETIC CONTROL LAWS AND STEADY STATE FLUX DISTRIBUTIONS. [Masters Thesis]. Cornell University; 2019. Available from: http://hdl.handle.net/1813/70034


Cornell University

2. Takahashi, Melissa. Developing Design Principles For Engineering Rna Transcription Regulators And Rna Synthetic Gene Networks.

Degree: PhD, Chemical Engineering, 2015, Cornell University

 A major goal of synthetic biology is to reliably engineer microorganisms to perform a variety of functions with impact in the fields of biotechnology and… (more)

Subjects/Keywords: RNA synthetic biology; transcription regulation

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APA (6th Edition):

Takahashi, M. (2015). Developing Design Principles For Engineering Rna Transcription Regulators And Rna Synthetic Gene Networks. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/41135

Chicago Manual of Style (16th Edition):

Takahashi, Melissa. “Developing Design Principles For Engineering Rna Transcription Regulators And Rna Synthetic Gene Networks.” 2015. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/41135.

MLA Handbook (7th Edition):

Takahashi, Melissa. “Developing Design Principles For Engineering Rna Transcription Regulators And Rna Synthetic Gene Networks.” 2015. Web. 07 May 2021.

Vancouver:

Takahashi M. Developing Design Principles For Engineering Rna Transcription Regulators And Rna Synthetic Gene Networks. [Internet] [Doctoral dissertation]. Cornell University; 2015. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/41135.

Council of Science Editors:

Takahashi M. Developing Design Principles For Engineering Rna Transcription Regulators And Rna Synthetic Gene Networks. [Doctoral Dissertation]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/41135


Cornell University

3. Loughrey, David Alan. Using SHAPE-Seq as a tool to understand RNA structure / function relationships.

Degree: PhD, Chemical Engineering, 2017, Cornell University

 RNA is a key player in many cellular processes. In both eukaryotes and prokaryotes, RNAs regulate gene expression by affecting transcription, translation, protein function, and… (more)

Subjects/Keywords: Chemical engineering; Next Generation Sequencing; RNA; SHAPE-Seq; Small Bacterial RNAs; Structomics; Structural Engineering; Biology; Biomedical engineering

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APA (6th Edition):

Loughrey, D. A. (2017). Using SHAPE-Seq as a tool to understand RNA structure / function relationships. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/47709

Chicago Manual of Style (16th Edition):

Loughrey, David Alan. “Using SHAPE-Seq as a tool to understand RNA structure / function relationships.” 2017. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/47709.

MLA Handbook (7th Edition):

Loughrey, David Alan. “Using SHAPE-Seq as a tool to understand RNA structure / function relationships.” 2017. Web. 07 May 2021.

Vancouver:

Loughrey DA. Using SHAPE-Seq as a tool to understand RNA structure / function relationships. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/47709.

Council of Science Editors:

Loughrey DA. Using SHAPE-Seq as a tool to understand RNA structure / function relationships. [Doctoral Dissertation]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/47709


Cornell University

4. Hsia, Chih-Yun. Studying Lipid-Protein Interaction Using Proteinacous Supported Lipid Bilayers from Cell Membranes.

Degree: PhD, Chemical Engineering, 2017, Cornell University

 Membrane proteins play important roles in cell biology and thus it is crucial to develop methods to access their functional information for further applications such… (more)

Subjects/Keywords: Biochemistry; Chemical engineering

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APA (6th Edition):

Hsia, C. (2017). Studying Lipid-Protein Interaction Using Proteinacous Supported Lipid Bilayers from Cell Membranes. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/47737

Chicago Manual of Style (16th Edition):

Hsia, Chih-Yun. “Studying Lipid-Protein Interaction Using Proteinacous Supported Lipid Bilayers from Cell Membranes.” 2017. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/47737.

MLA Handbook (7th Edition):

Hsia, Chih-Yun. “Studying Lipid-Protein Interaction Using Proteinacous Supported Lipid Bilayers from Cell Membranes.” 2017. Web. 07 May 2021.

Vancouver:

Hsia C. Studying Lipid-Protein Interaction Using Proteinacous Supported Lipid Bilayers from Cell Membranes. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/47737.

Council of Science Editors:

Hsia C. Studying Lipid-Protein Interaction Using Proteinacous Supported Lipid Bilayers from Cell Membranes. [Doctoral Dissertation]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/47737


Cornell University

5. Chen, Feng-Yang. Engineered Oligosaccharyltransferases With Unique N-Glycosylation Site Preferences.

Degree: M.S., Chemical Engineering, Chemical Engineering, 2019, Cornell University

 The key enzyme in the Campylobacter jejuni glycosylation pathway, PglB, has been one of the well-studied asparagine-linked oligosaccharyltransferase (OST) in bacterial glycoengineering area. While C.… (more)

Subjects/Keywords: Chemical engineering; Campylobacter jejuni; Desulfovibrio desulfuricans; Glycosylation; Oligosaccharyltransferases; PglB; sequon logo; Biomedical engineering

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APA (6th Edition):

Chen, F. (2019). Engineered Oligosaccharyltransferases With Unique N-Glycosylation Site Preferences. (Masters Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/67663

Chicago Manual of Style (16th Edition):

Chen, Feng-Yang. “Engineered Oligosaccharyltransferases With Unique N-Glycosylation Site Preferences.” 2019. Masters Thesis, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/67663.

MLA Handbook (7th Edition):

Chen, Feng-Yang. “Engineered Oligosaccharyltransferases With Unique N-Glycosylation Site Preferences.” 2019. Web. 07 May 2021.

Vancouver:

Chen F. Engineered Oligosaccharyltransferases With Unique N-Glycosylation Site Preferences. [Internet] [Masters thesis]. Cornell University; 2019. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/67663.

Council of Science Editors:

Chen F. Engineered Oligosaccharyltransferases With Unique N-Glycosylation Site Preferences. [Masters Thesis]. Cornell University; 2019. Available from: http://hdl.handle.net/1813/67663


Cornell University

6. Walker, Joshua Aaron. Multifunctional Chemical Cross-linkers for Drug Carriers and Molecular Probes.

Degree: PhD, Chemical Engineering, 2019, Cornell University

 Bioconjugates are an indispensable tool for molecular biology as well as an established modality for biomedical imaging and drug delivery. Broadly, bioconjugation is the use… (more)

Subjects/Keywords: Chemical engineering; Antibody-drug Conjugates; Bioconjugates; Click Chemistry; Sequence-defined Polymers; siRNA Therapeutics; Site-specific Protein Modification; Chemistry; Bioengineering

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APA (6th Edition):

Walker, J. A. (2019). Multifunctional Chemical Cross-linkers for Drug Carriers and Molecular Probes. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/67559

Chicago Manual of Style (16th Edition):

Walker, Joshua Aaron. “Multifunctional Chemical Cross-linkers for Drug Carriers and Molecular Probes.” 2019. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/67559.

MLA Handbook (7th Edition):

Walker, Joshua Aaron. “Multifunctional Chemical Cross-linkers for Drug Carriers and Molecular Probes.” 2019. Web. 07 May 2021.

Vancouver:

Walker JA. Multifunctional Chemical Cross-linkers for Drug Carriers and Molecular Probes. [Internet] [Doctoral dissertation]. Cornell University; 2019. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/67559.

Council of Science Editors:

Walker JA. Multifunctional Chemical Cross-linkers for Drug Carriers and Molecular Probes. [Doctoral Dissertation]. Cornell University; 2019. Available from: http://hdl.handle.net/1813/67559


Cornell University

7. Meksiriporn, Bunyarit. DIRECT INTRACELLULAR SELECTION OF SYNTHETIC BINDING PROTEINS THAT SPECIFICALLY RECOGNIZE POST-TRANSLATIONALLY MODIFIED PROTEINS.

Degree: PhD, Biomedical Engineering, 2018, Cornell University

 Post-translational modifications (PTMs), such as phosphate groups, control many cellular activities and play important roles in both health and disease. Accordingly, there is an urgent… (more)

Subjects/Keywords: Post-translational modifications; protein engineering; Biomedical engineering; Molecular biology; DARPins; FLI-TRAP; PhLI-TRAP; phosphorylation; Bioengineering

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APA (6th Edition):

Meksiriporn, B. (2018). DIRECT INTRACELLULAR SELECTION OF SYNTHETIC BINDING PROTEINS THAT SPECIFICALLY RECOGNIZE POST-TRANSLATIONALLY MODIFIED PROTEINS. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/64887

Chicago Manual of Style (16th Edition):

Meksiriporn, Bunyarit. “DIRECT INTRACELLULAR SELECTION OF SYNTHETIC BINDING PROTEINS THAT SPECIFICALLY RECOGNIZE POST-TRANSLATIONALLY MODIFIED PROTEINS.” 2018. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/64887.

MLA Handbook (7th Edition):

Meksiriporn, Bunyarit. “DIRECT INTRACELLULAR SELECTION OF SYNTHETIC BINDING PROTEINS THAT SPECIFICALLY RECOGNIZE POST-TRANSLATIONALLY MODIFIED PROTEINS.” 2018. Web. 07 May 2021.

Vancouver:

Meksiriporn B. DIRECT INTRACELLULAR SELECTION OF SYNTHETIC BINDING PROTEINS THAT SPECIFICALLY RECOGNIZE POST-TRANSLATIONALLY MODIFIED PROTEINS. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/64887.

Council of Science Editors:

Meksiriporn B. DIRECT INTRACELLULAR SELECTION OF SYNTHETIC BINDING PROTEINS THAT SPECIFICALLY RECOGNIZE POST-TRANSLATIONALLY MODIFIED PROTEINS. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/64887


Cornell University

8. Li, Jiahe. Blood-Borne Cancer Metastasis: From Mechanisms To Therapeutics.

Degree: PhD, Biomedical Engineering, 2015, Cornell University

 Metastasis is the cause of about 90% of cancer-associated deaths, yet the mechanisms governing this clinically important process remain poorly understood. Distant metastases rely on… (more)

Subjects/Keywords: Circulating tumor cells; Metastasis; Therapy

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APA (6th Edition):

Li, J. (2015). Blood-Borne Cancer Metastasis: From Mechanisms To Therapeutics. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/41110

Chicago Manual of Style (16th Edition):

Li, Jiahe. “Blood-Borne Cancer Metastasis: From Mechanisms To Therapeutics.” 2015. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/41110.

MLA Handbook (7th Edition):

Li, Jiahe. “Blood-Borne Cancer Metastasis: From Mechanisms To Therapeutics.” 2015. Web. 07 May 2021.

Vancouver:

Li J. Blood-Borne Cancer Metastasis: From Mechanisms To Therapeutics. [Internet] [Doctoral dissertation]. Cornell University; 2015. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/41110.

Council of Science Editors:

Li J. Blood-Borne Cancer Metastasis: From Mechanisms To Therapeutics. [Doctoral Dissertation]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/41110


Cornell University

9. O'Brien, Sean. Developing A Ubiquitin-Like Modification Reporter.

Degree: PhD, Chemical Engineering, 2013, Cornell University

 Ubiquitin-like (ubl) modification is an example of post-translational modification (PTM) that influences a number of cellular processes. Given difficulties in studying this system in its… (more)

Subjects/Keywords: ubiquitin; SUMO; Cre; PCA; E. coli; plasmid display; ubiquitination; sumoylation; protein engieering

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APA (6th Edition):

O'Brien, S. (2013). Developing A Ubiquitin-Like Modification Reporter. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/34080

Chicago Manual of Style (16th Edition):

O'Brien, Sean. “Developing A Ubiquitin-Like Modification Reporter.” 2013. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/34080.

MLA Handbook (7th Edition):

O'Brien, Sean. “Developing A Ubiquitin-Like Modification Reporter.” 2013. Web. 07 May 2021.

Vancouver:

O'Brien S. Developing A Ubiquitin-Like Modification Reporter. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/34080.

Council of Science Editors:

O'Brien S. Developing A Ubiquitin-Like Modification Reporter. [Doctoral Dissertation]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/34080


Cornell University

10. Prabhu, Sudhir. Using Ionic Strength To Modulate Lipid Diffusion In Solid-Supported Lipid Bilayers.

Degree: M.S., Chemical Engineering, Chemical Engineering, 2011, Cornell University

 Solid-supported lipid bilayers (SLBs) are an ideal model system to study natural cell membranes. They can be used as a medium for protein separation, a… (more)

Subjects/Keywords: membrane fluidity; lipid mobility; planar bilayer

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APA (6th Edition):

Prabhu, S. (2011). Using Ionic Strength To Modulate Lipid Diffusion In Solid-Supported Lipid Bilayers. (Masters Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/29489

Chicago Manual of Style (16th Edition):

Prabhu, Sudhir. “Using Ionic Strength To Modulate Lipid Diffusion In Solid-Supported Lipid Bilayers.” 2011. Masters Thesis, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/29489.

MLA Handbook (7th Edition):

Prabhu, Sudhir. “Using Ionic Strength To Modulate Lipid Diffusion In Solid-Supported Lipid Bilayers.” 2011. Web. 07 May 2021.

Vancouver:

Prabhu S. Using Ionic Strength To Modulate Lipid Diffusion In Solid-Supported Lipid Bilayers. [Internet] [Masters thesis]. Cornell University; 2011. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/29489.

Council of Science Editors:

Prabhu S. Using Ionic Strength To Modulate Lipid Diffusion In Solid-Supported Lipid Bilayers. [Masters Thesis]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/29489


Cornell University

11. Haitjema, Charles. Engineering Extracellular Secretion Pathways In Escherichia Coli.

Degree: PhD, Microbiology, 2012, Cornell University

 Extracellular secretion is highly desirable in preparative protein production. The bacterium Escherichia coli is a commonly used for both laboratory- and industrial- scale biosynthesis of… (more)

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APA (6th Edition):

Haitjema, C. (2012). Engineering Extracellular Secretion Pathways In Escherichia Coli. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/30993

Chicago Manual of Style (16th Edition):

Haitjema, Charles. “Engineering Extracellular Secretion Pathways In Escherichia Coli.” 2012. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/30993.

MLA Handbook (7th Edition):

Haitjema, Charles. “Engineering Extracellular Secretion Pathways In Escherichia Coli.” 2012. Web. 07 May 2021.

Vancouver:

Haitjema C. Engineering Extracellular Secretion Pathways In Escherichia Coli. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/30993.

Council of Science Editors:

Haitjema C. Engineering Extracellular Secretion Pathways In Escherichia Coli. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/30993


Cornell University

12. Bardliving, Cameron. Development Of Micro And Nanoparticle Substrates For Sers Detection Of Pesticides And Delivery Of Chemotherapeutic Drugs And Pilot Scale Process Development And Cgmp Production Of Cancer Testis Antigen Melan-A.

Degree: PhD, Biomedical Engineering, 2013, Cornell University

 Detection or delivery of a diverse range of biomolecules in field portable devices is an important area of research in the fields of environmental pollution,… (more)

Subjects/Keywords: Surface Enhance Raman Spectroscopy; Molecularly Imprinted Polymers; Cancer Testes Antigens

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APA (6th Edition):

Bardliving, C. (2013). Development Of Micro And Nanoparticle Substrates For Sers Detection Of Pesticides And Delivery Of Chemotherapeutic Drugs And Pilot Scale Process Development And Cgmp Production Of Cancer Testis Antigen Melan-A. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/33986

Chicago Manual of Style (16th Edition):

Bardliving, Cameron. “Development Of Micro And Nanoparticle Substrates For Sers Detection Of Pesticides And Delivery Of Chemotherapeutic Drugs And Pilot Scale Process Development And Cgmp Production Of Cancer Testis Antigen Melan-A.” 2013. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/33986.

MLA Handbook (7th Edition):

Bardliving, Cameron. “Development Of Micro And Nanoparticle Substrates For Sers Detection Of Pesticides And Delivery Of Chemotherapeutic Drugs And Pilot Scale Process Development And Cgmp Production Of Cancer Testis Antigen Melan-A.” 2013. Web. 07 May 2021.

Vancouver:

Bardliving C. Development Of Micro And Nanoparticle Substrates For Sers Detection Of Pesticides And Delivery Of Chemotherapeutic Drugs And Pilot Scale Process Development And Cgmp Production Of Cancer Testis Antigen Melan-A. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/33986.

Council of Science Editors:

Bardliving C. Development Of Micro And Nanoparticle Substrates For Sers Detection Of Pesticides And Delivery Of Chemotherapeutic Drugs And Pilot Scale Process Development And Cgmp Production Of Cancer Testis Antigen Melan-A. [Doctoral Dissertation]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/33986


Cornell University

13. Robinson, Michael-Paul. Remodeling Antibodies from the Inside Out: Functional Engineering of Full-Length Antibodies in the Cytoplasm of Bacteria.

Degree: PhD, Chemical Engineering, 2017, Cornell University

 Antibodies are indispensable tools in many research, diagnostic, and clinical applications. Current methods for producing immunoglobulin G (IgG) antibodies in engineered cells often require refolding… (more)

Subjects/Keywords: E. coli; Chemical engineering; Immunology; Cellular biology; antibodies; antibody engineering; cyclonals; Full-length; immunoglobulin

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APA (6th Edition):

Robinson, M. (2017). Remodeling Antibodies from the Inside Out: Functional Engineering of Full-Length Antibodies in the Cytoplasm of Bacteria. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59085

Chicago Manual of Style (16th Edition):

Robinson, Michael-Paul. “Remodeling Antibodies from the Inside Out: Functional Engineering of Full-Length Antibodies in the Cytoplasm of Bacteria.” 2017. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/59085.

MLA Handbook (7th Edition):

Robinson, Michael-Paul. “Remodeling Antibodies from the Inside Out: Functional Engineering of Full-Length Antibodies in the Cytoplasm of Bacteria.” 2017. Web. 07 May 2021.

Vancouver:

Robinson M. Remodeling Antibodies from the Inside Out: Functional Engineering of Full-Length Antibodies in the Cytoplasm of Bacteria. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/59085.

Council of Science Editors:

Robinson M. Remodeling Antibodies from the Inside Out: Functional Engineering of Full-Length Antibodies in the Cytoplasm of Bacteria. [Doctoral Dissertation]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/59085


Cornell University

14. Horvath, Nicholas. Kinetic and constraint-based modeling of E. coli based cell-free protein synthesis.

Degree: PhD, Chemical Engineering, 2019, Cornell University

 Cell-free protein synthesis is a powerful technology for applications ranging from therapeutics to synthetic biology. Cells are lysed to produce an extract that is used… (more)

Subjects/Keywords: cell-free; mathematical modeling; microfluidic; systems biology

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APA (6th Edition):

Horvath, N. (2019). Kinetic and constraint-based modeling of E. coli based cell-free protein synthesis. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/70130

Chicago Manual of Style (16th Edition):

Horvath, Nicholas. “Kinetic and constraint-based modeling of E. coli based cell-free protein synthesis.” 2019. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/70130.

MLA Handbook (7th Edition):

Horvath, Nicholas. “Kinetic and constraint-based modeling of E. coli based cell-free protein synthesis.” 2019. Web. 07 May 2021.

Vancouver:

Horvath N. Kinetic and constraint-based modeling of E. coli based cell-free protein synthesis. [Internet] [Doctoral dissertation]. Cornell University; 2019. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/70130.

Council of Science Editors:

Horvath N. Kinetic and constraint-based modeling of E. coli based cell-free protein synthesis. [Doctoral Dissertation]. Cornell University; 2019. Available from: http://hdl.handle.net/1813/70130


Cornell University

15. Chakrabarti, Anirikh. Systems Analysis Of Core Architectures Regulating Cellular Responses Under Stress In Eukaryotes.

Degree: PhD, Chemical Engineering, 2012, Cornell University

 Eukaryotes have developed evolutionarily conserved mechanisms to respond to diverse ranges of internal and external perturbations e.g., changes in oxygen/nutrient levels, temperature oscillations, protein folding… (more)

Subjects/Keywords: Hypoxia; upr; emt; Multiscale Modeling; Sensitivity Analysis; Robustness; Cellular Stress

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APA (6th Edition):

Chakrabarti, A. (2012). Systems Analysis Of Core Architectures Regulating Cellular Responses Under Stress In Eukaryotes. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/29190

Chicago Manual of Style (16th Edition):

Chakrabarti, Anirikh. “Systems Analysis Of Core Architectures Regulating Cellular Responses Under Stress In Eukaryotes.” 2012. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/29190.

MLA Handbook (7th Edition):

Chakrabarti, Anirikh. “Systems Analysis Of Core Architectures Regulating Cellular Responses Under Stress In Eukaryotes.” 2012. Web. 07 May 2021.

Vancouver:

Chakrabarti A. Systems Analysis Of Core Architectures Regulating Cellular Responses Under Stress In Eukaryotes. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/29190.

Council of Science Editors:

Chakrabarti A. Systems Analysis Of Core Architectures Regulating Cellular Responses Under Stress In Eukaryotes. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/29190


Cornell University

16. Rocco, Mark. Twin-Arginine Translocase Mutations That Suppress Folding Quality Control And Permit Export Of Misfolded Substrate Proteins.

Degree: PhD, Biomedical Engineering, 2011, Cornell University

 The twin-arginine translocation (Tat) pathway is a robust protein translocation system capable of transporting cellular proteins across the bacterial cytoplasmic membrane. A hallmark of the… (more)

Subjects/Keywords: Twin-Arginine Translocation (Tat); Folding Quality Control; Escherichia coli

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APA (6th Edition):

Rocco, M. (2011). Twin-Arginine Translocase Mutations That Suppress Folding Quality Control And Permit Export Of Misfolded Substrate Proteins. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/29403

Chicago Manual of Style (16th Edition):

Rocco, Mark. “Twin-Arginine Translocase Mutations That Suppress Folding Quality Control And Permit Export Of Misfolded Substrate Proteins.” 2011. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/29403.

MLA Handbook (7th Edition):

Rocco, Mark. “Twin-Arginine Translocase Mutations That Suppress Folding Quality Control And Permit Export Of Misfolded Substrate Proteins.” 2011. Web. 07 May 2021.

Vancouver:

Rocco M. Twin-Arginine Translocase Mutations That Suppress Folding Quality Control And Permit Export Of Misfolded Substrate Proteins. [Internet] [Doctoral dissertation]. Cornell University; 2011. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/29403.

Council of Science Editors:

Rocco M. Twin-Arginine Translocase Mutations That Suppress Folding Quality Control And Permit Export Of Misfolded Substrate Proteins. [Doctoral Dissertation]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/29403


Cornell University

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

Degree: PhD, Chemical Engineering, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/67803

Chicago Manual of Style (16th Edition):

Ludwicki, Morgan Baltz. “BROAD-SPECTRUM PROTEOME EDITING WITH AN ENGINEERED BACTERIAL UBIQUITIN LIGASE MIMIC.” 2019. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/67803.

MLA Handbook (7th Edition):

Ludwicki, Morgan Baltz. “BROAD-SPECTRUM PROTEOME EDITING WITH AN ENGINEERED BACTERIAL UBIQUITIN LIGASE MIMIC.” 2019. Web. 07 May 2021.

Vancouver:

Ludwicki MB. BROAD-SPECTRUM PROTEOME EDITING WITH AN ENGINEERED BACTERIAL UBIQUITIN LIGASE MIMIC. [Internet] [Doctoral dissertation]. Cornell University; 2019. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/67803.

Council of Science Editors:

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


Cornell University

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

Degree: PhD, Chemical Engineering, 2012, Cornell University

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

Subjects/Keywords: Protein Engineering; Bacteria; Glycosylation

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Mansell, Thomas. “A Suite Of Tools For Reporting And Engineering Protein Folding, Interactions, And Post-Translational Modifications In The Bacterial Periplasm.” 2012. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/29502.

MLA Handbook (7th Edition):

Mansell, Thomas. “A Suite Of Tools For Reporting And Engineering Protein Folding, Interactions, And Post-Translational Modifications In The Bacterial Periplasm.” 2012. Web. 07 May 2021.

Vancouver:

Mansell T. A Suite Of Tools For Reporting And Engineering Protein Folding, Interactions, And Post-Translational Modifications In The Bacterial Periplasm. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/29502.

Council of Science Editors:

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


Cornell University

19. Watkins, Hannah Christine. Recombinant Escherichia coli derived outer membrane vesicles for safe and effective subunit antigen delivery.

Degree: PhD, Biomedical Engineering, 2017, Cornell University

 Subunit vaccines rely on adjuvants to drive an immune response against antigens of interest. Improved adjuvant platforms, capable of interaction with specific pathogen recognition receptors… (more)

Subjects/Keywords: E. coli; Immunology; Biomedical engineering; vaccine; Influenza; Lipopolysaccharide; M2e; Outer membrane vesicle; Virology

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APA (6th Edition):

Watkins, H. C. (2017). Recombinant Escherichia coli derived outer membrane vesicles for safe and effective subunit antigen delivery. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/47843

Chicago Manual of Style (16th Edition):

Watkins, Hannah Christine. “Recombinant Escherichia coli derived outer membrane vesicles for safe and effective subunit antigen delivery.” 2017. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/47843.

MLA Handbook (7th Edition):

Watkins, Hannah Christine. “Recombinant Escherichia coli derived outer membrane vesicles for safe and effective subunit antigen delivery.” 2017. Web. 07 May 2021.

Vancouver:

Watkins HC. Recombinant Escherichia coli derived outer membrane vesicles for safe and effective subunit antigen delivery. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/47843.

Council of Science Editors:

Watkins HC. Recombinant Escherichia coli derived outer membrane vesicles for safe and effective subunit antigen delivery. [Doctoral Dissertation]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/47843


Cornell University

20. Borde, Brandon. REPAIR OF FOCAL DEFECTS IN THE ANNULUS FIBROSUS USING AN IN SITU-PHOTOCROSSLINKABLE COLLAGEN HYDROGEL.

Degree: PhD, Biomedical Engineering, 2017, Cornell University

 The intervertebral disc (IVD) is a cartilaginous structure in the spinal column comprised of the inner nucleus pulposus (NP) and the outer annulus fibrosus (AF).… (more)

Subjects/Keywords: Intervertebral Disc; Biomedical engineering; Biomechanics; Annulus Fibrosus; Collagen Gel; Engineering

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APA (6th Edition):

Borde, B. (2017). REPAIR OF FOCAL DEFECTS IN THE ANNULUS FIBROSUS USING AN IN SITU-PHOTOCROSSLINKABLE COLLAGEN HYDROGEL. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/47844

Chicago Manual of Style (16th Edition):

Borde, Brandon. “REPAIR OF FOCAL DEFECTS IN THE ANNULUS FIBROSUS USING AN IN SITU-PHOTOCROSSLINKABLE COLLAGEN HYDROGEL.” 2017. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/47844.

MLA Handbook (7th Edition):

Borde, Brandon. “REPAIR OF FOCAL DEFECTS IN THE ANNULUS FIBROSUS USING AN IN SITU-PHOTOCROSSLINKABLE COLLAGEN HYDROGEL.” 2017. Web. 07 May 2021.

Vancouver:

Borde B. REPAIR OF FOCAL DEFECTS IN THE ANNULUS FIBROSUS USING AN IN SITU-PHOTOCROSSLINKABLE COLLAGEN HYDROGEL. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/47844.

Council of Science Editors:

Borde B. REPAIR OF FOCAL DEFECTS IN THE ANNULUS FIBROSUS USING AN IN SITU-PHOTOCROSSLINKABLE COLLAGEN HYDROGEL. [Doctoral Dissertation]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/47844


Cornell University

21. Valderrama Rincon, Juan. Engineering Eukaryotic-Like Protein Glycosylation In Escherichia Coli.

Degree: PhD, Chemical Engineering, 2012, Cornell University

 N-linked glycosylation is a common protein post-translational modification where glycans are attached to asparagine residues located on a consensus sequence. Structure of these glycans varies… (more)

Subjects/Keywords: escherichia coli; protein glycosylation; glycan

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APA (6th Edition):

Valderrama Rincon, J. (2012). Engineering Eukaryotic-Like Protein Glycosylation In Escherichia Coli. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/31437

Chicago Manual of Style (16th Edition):

Valderrama Rincon, Juan. “Engineering Eukaryotic-Like Protein Glycosylation In Escherichia Coli.” 2012. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/31437.

MLA Handbook (7th Edition):

Valderrama Rincon, Juan. “Engineering Eukaryotic-Like Protein Glycosylation In Escherichia Coli.” 2012. Web. 07 May 2021.

Vancouver:

Valderrama Rincon J. Engineering Eukaryotic-Like Protein Glycosylation In Escherichia Coli. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/31437.

Council of Science Editors:

Valderrama Rincon J. Engineering Eukaryotic-Like Protein Glycosylation In Escherichia Coli. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/31437


Cornell University

22. Stevenson, Taylor Currie. ENGINEERING BACTERIAL GLYCOBIOLOGY FOR THE CREATION OF GLYCOCONJUGATE VACCINES.

Degree: PhD, Biomedical Engineering, 2017, Cornell University

 The use of vaccines has led to the effective eradication of several human diseases which were once epidemic such as smallpox and polio. Vaccines have… (more)

Subjects/Keywords: Chemical engineering; Biomedical engineering; glycobiolology; glycoconjugate; OMV; PNAG; polysaccharide; vaccine

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APA (6th Edition):

Stevenson, T. C. (2017). ENGINEERING BACTERIAL GLYCOBIOLOGY FOR THE CREATION OF GLYCOCONJUGATE VACCINES. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/47799

Chicago Manual of Style (16th Edition):

Stevenson, Taylor Currie. “ENGINEERING BACTERIAL GLYCOBIOLOGY FOR THE CREATION OF GLYCOCONJUGATE VACCINES.” 2017. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/47799.

MLA Handbook (7th Edition):

Stevenson, Taylor Currie. “ENGINEERING BACTERIAL GLYCOBIOLOGY FOR THE CREATION OF GLYCOCONJUGATE VACCINES.” 2017. Web. 07 May 2021.

Vancouver:

Stevenson TC. ENGINEERING BACTERIAL GLYCOBIOLOGY FOR THE CREATION OF GLYCOCONJUGATE VACCINES. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/47799.

Council of Science Editors:

Stevenson TC. ENGINEERING BACTERIAL GLYCOBIOLOGY FOR THE CREATION OF GLYCOCONJUGATE VACCINES. [Doctoral Dissertation]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/47799


Cornell University

23. Lowe, Adam. Development Of Bio-Nanotechnology Systems For Sers Based Detection Of Bio-Molecules.

Degree: PhD, Microbiology, 2011, Cornell University

 Targeted detection of bio-molecules in vivo and in the environment is a key area of research. Surface enhanced Raman spectroscopy (SERS) is emerging as a… (more)

Subjects/Keywords: sers; intein; ldr

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APA (6th Edition):

Lowe, A. (2011). Development Of Bio-Nanotechnology Systems For Sers Based Detection Of Bio-Molecules. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/30603

Chicago Manual of Style (16th Edition):

Lowe, Adam. “Development Of Bio-Nanotechnology Systems For Sers Based Detection Of Bio-Molecules.” 2011. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/30603.

MLA Handbook (7th Edition):

Lowe, Adam. “Development Of Bio-Nanotechnology Systems For Sers Based Detection Of Bio-Molecules.” 2011. Web. 07 May 2021.

Vancouver:

Lowe A. Development Of Bio-Nanotechnology Systems For Sers Based Detection Of Bio-Molecules. [Internet] [Doctoral dissertation]. Cornell University; 2011. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/30603.

Council of Science Editors:

Lowe A. Development Of Bio-Nanotechnology Systems For Sers Based Detection Of Bio-Molecules. [Doctoral Dissertation]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/30603


Cornell University

24. Portnoff, Alyse. Ubiquibodies: Engineered Ubiquitin Ligases With Unnatural Substrate Specificity For Targeted Protein Silencing.

Degree: PhD, Biomedical Engineering, 2014, Cornell University

 The ubiquitin-proteasome pathway (UPP) is the main route of protein degradation in eukaryotic cells and aids in regulation of cell cycle and cellular homeostasis. This… (more)

Subjects/Keywords: protein engineering; targeted proteolysis; reverse genetics

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APA (6th Edition):

Portnoff, A. (2014). Ubiquibodies: Engineered Ubiquitin Ligases With Unnatural Substrate Specificity For Targeted Protein Silencing. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/36040

Chicago Manual of Style (16th Edition):

Portnoff, Alyse. “Ubiquibodies: Engineered Ubiquitin Ligases With Unnatural Substrate Specificity For Targeted Protein Silencing.” 2014. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/36040.

MLA Handbook (7th Edition):

Portnoff, Alyse. “Ubiquibodies: Engineered Ubiquitin Ligases With Unnatural Substrate Specificity For Targeted Protein Silencing.” 2014. Web. 07 May 2021.

Vancouver:

Portnoff A. Ubiquibodies: Engineered Ubiquitin Ligases With Unnatural Substrate Specificity For Targeted Protein Silencing. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/36040.

Council of Science Editors:

Portnoff A. Ubiquibodies: Engineered Ubiquitin Ligases With Unnatural Substrate Specificity For Targeted Protein Silencing. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/36040


Cornell University

25. Vadhin, Sandra. TOWARD A MICROFLUIDIC PLATFORM FOR CELL FREE SYNTHESIS OF MORPHINE DEGRADATION PATHWAY ENZYMES.

Degree: M.S., Chemical Engineering, Chemical Engineering, 2020, Cornell University

 Opioids are a class of drugs highly valued for their potent analgesic properties; however, they are also highly addictive and cause severe side effects. Alternative… (more)

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APA (6th Edition):

Vadhin, S. (2020). TOWARD A MICROFLUIDIC PLATFORM FOR CELL FREE SYNTHESIS OF MORPHINE DEGRADATION PATHWAY ENZYMES. (Masters Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/103284

Chicago Manual of Style (16th Edition):

Vadhin, Sandra. “TOWARD A MICROFLUIDIC PLATFORM FOR CELL FREE SYNTHESIS OF MORPHINE DEGRADATION PATHWAY ENZYMES.” 2020. Masters Thesis, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/103284.

MLA Handbook (7th Edition):

Vadhin, Sandra. “TOWARD A MICROFLUIDIC PLATFORM FOR CELL FREE SYNTHESIS OF MORPHINE DEGRADATION PATHWAY ENZYMES.” 2020. Web. 07 May 2021.

Vancouver:

Vadhin S. TOWARD A MICROFLUIDIC PLATFORM FOR CELL FREE SYNTHESIS OF MORPHINE DEGRADATION PATHWAY ENZYMES. [Internet] [Masters thesis]. Cornell University; 2020. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/103284.

Council of Science Editors:

Vadhin S. TOWARD A MICROFLUIDIC PLATFORM FOR CELL FREE SYNTHESIS OF MORPHINE DEGRADATION PATHWAY ENZYMES. [Masters Thesis]. Cornell University; 2020. Available from: http://hdl.handle.net/1813/103284


Cornell University

26. Boock, Jason. Expanding The Capabilities Of A Bacterial Quality Control Mechanism For Engineering Enzymes.

Degree: PhD, Chemical Engineering, 2015, Cornell University

 In this study, we have repurposed the intrinsic quality control of the twin-arginine translocation (Tat) pathway to enhance the traits of target proteins using directed… (more)

Subjects/Keywords: Protein engineering; Cellular quality control; Heterologous cellulase production

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APA (6th Edition):

Boock, J. (2015). Expanding The Capabilities Of A Bacterial Quality Control Mechanism For Engineering Enzymes. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/39363

Chicago Manual of Style (16th Edition):

Boock, Jason. “Expanding The Capabilities Of A Bacterial Quality Control Mechanism For Engineering Enzymes.” 2015. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/39363.

MLA Handbook (7th Edition):

Boock, Jason. “Expanding The Capabilities Of A Bacterial Quality Control Mechanism For Engineering Enzymes.” 2015. Web. 07 May 2021.

Vancouver:

Boock J. Expanding The Capabilities Of A Bacterial Quality Control Mechanism For Engineering Enzymes. [Internet] [Doctoral dissertation]. Cornell University; 2015. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/39363.

Council of Science Editors:

Boock J. Expanding The Capabilities Of A Bacterial Quality Control Mechanism For Engineering Enzymes. [Doctoral Dissertation]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/39363


Cornell University

27. Doud, Devin. Engineering Applications Using The Innate Redox Environment Of Rhodopseudomonas Palustris.

Degree: PhD, Microbiology, 2014, Cornell University

 Rhodopseudomonas palustris is currently the most metabolically versatile organism known. Because of this, it has become a model organism not only for it's many forms… (more)

Subjects/Keywords: Rhodopseudomonas palustris; Microbial Electrochemistry; Metabolic Engineering

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APA (6th Edition):

Doud, D. (2014). Engineering Applications Using The Innate Redox Environment Of Rhodopseudomonas Palustris. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/38792

Chicago Manual of Style (16th Edition):

Doud, Devin. “Engineering Applications Using The Innate Redox Environment Of Rhodopseudomonas Palustris.” 2014. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/38792.

MLA Handbook (7th Edition):

Doud, Devin. “Engineering Applications Using The Innate Redox Environment Of Rhodopseudomonas Palustris.” 2014. Web. 07 May 2021.

Vancouver:

Doud D. Engineering Applications Using The Innate Redox Environment Of Rhodopseudomonas Palustris. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/38792.

Council of Science Editors:

Doud D. Engineering Applications Using The Innate Redox Environment Of Rhodopseudomonas Palustris. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/38792


Cornell University

28. Guarino, Cassandra. Investigating Oligosaccharyltransferases Of N-Linked Glycosylation Using Escherichia Coli.

Degree: PhD, Veterinary Medicine, 2013, Cornell University

 Escherichia coli is a powerful tool for elucidating many of the basic principles of biology. As a protein production host, E. coli can produce exogenous… (more)

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APA (6th Edition):

Guarino, C. (2013). Investigating Oligosaccharyltransferases Of N-Linked Glycosylation Using Escherichia Coli. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/33830

Chicago Manual of Style (16th Edition):

Guarino, Cassandra. “Investigating Oligosaccharyltransferases Of N-Linked Glycosylation Using Escherichia Coli.” 2013. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/33830.

MLA Handbook (7th Edition):

Guarino, Cassandra. “Investigating Oligosaccharyltransferases Of N-Linked Glycosylation Using Escherichia Coli.” 2013. Web. 07 May 2021.

Vancouver:

Guarino C. Investigating Oligosaccharyltransferases Of N-Linked Glycosylation Using Escherichia Coli. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/33830.

Council of Science Editors:

Guarino C. Investigating Oligosaccharyltransferases Of N-Linked Glycosylation Using Escherichia Coli. [Doctoral Dissertation]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/33830


Cornell University

29. Yang, Dong. Assessing The Influence Of Biomass Accessibility On Enzyme Transport And Catalysis.

Degree: PhD, Agricultural and Biological Engineering, 2014, Cornell University

 Accessible internal pore surface is a major factor in defining the rate and extent of enzymatic hydrolysis of cellulosic biomass. Steric hindrance within the pore… (more)

Subjects/Keywords: size-exclusion chromatography; specific pore volume; specific surface area; accessibility

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APA (6th Edition):

Yang, D. (2014). Assessing The Influence Of Biomass Accessibility On Enzyme Transport And Catalysis. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/38800

Chicago Manual of Style (16th Edition):

Yang, Dong. “Assessing The Influence Of Biomass Accessibility On Enzyme Transport And Catalysis.” 2014. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/38800.

MLA Handbook (7th Edition):

Yang, Dong. “Assessing The Influence Of Biomass Accessibility On Enzyme Transport And Catalysis.” 2014. Web. 07 May 2021.

Vancouver:

Yang D. Assessing The Influence Of Biomass Accessibility On Enzyme Transport And Catalysis. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/38800.

Council of Science Editors:

Yang D. Assessing The Influence Of Biomass Accessibility On Enzyme Transport And Catalysis. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/38800


Cornell University

30. Barcus, Matthew. KINETICS AND STRUCTURAL CHARACTERIZATION OF LIPOLYTIC ENZYMES FOR HYDROLYZING POULTRY FEATHERS.

Degree: PhD, Animal Science, 2017, Cornell University

 The processing of chicken feathers poses a challenge for the poultry industry. In the USA, near 9 billion chickens are slaughtered annually, which generates 5… (more)

Subjects/Keywords: Biophysics; enzymology; feathers; lipase; protein engineering; wax; Biochemistry; Molecular biology; sustainability

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APA (6th Edition):

Barcus, M. (2017). KINETICS AND STRUCTURAL CHARACTERIZATION OF LIPOLYTIC ENZYMES FOR HYDROLYZING POULTRY FEATHERS. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/56755

Chicago Manual of Style (16th Edition):

Barcus, Matthew. “KINETICS AND STRUCTURAL CHARACTERIZATION OF LIPOLYTIC ENZYMES FOR HYDROLYZING POULTRY FEATHERS.” 2017. Doctoral Dissertation, Cornell University. Accessed May 07, 2021. http://hdl.handle.net/1813/56755.

MLA Handbook (7th Edition):

Barcus, Matthew. “KINETICS AND STRUCTURAL CHARACTERIZATION OF LIPOLYTIC ENZYMES FOR HYDROLYZING POULTRY FEATHERS.” 2017. Web. 07 May 2021.

Vancouver:

Barcus M. KINETICS AND STRUCTURAL CHARACTERIZATION OF LIPOLYTIC ENZYMES FOR HYDROLYZING POULTRY FEATHERS. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2021 May 07]. Available from: http://hdl.handle.net/1813/56755.

Council of Science Editors:

Barcus M. KINETICS AND STRUCTURAL CHARACTERIZATION OF LIPOLYTIC ENZYMES FOR HYDROLYZING POULTRY FEATHERS. [Doctoral Dissertation]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/56755

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