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University: University of Colorado

You searched for subject:(Protein Engineering). Showing records 1 – 18 of 18 total matches.

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University of Colorado

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

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

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Cordes, Amanda. “Complex Stability Behavior in Novel Protein Constructs: Aggregation of Fc- and HSA- Based Fusion Proteins.” 2011. Doctoral Dissertation, University of Colorado. Accessed July 08, 2020. https://scholar.colorado.edu/chbe_gradetds/20.

MLA Handbook (7th Edition):

Cordes, Amanda. “Complex Stability Behavior in Novel Protein Constructs: Aggregation of Fc- and HSA- Based Fusion Proteins.” 2011. Web. 08 Jul 2020.

Vancouver:

Cordes A. Complex Stability Behavior in Novel Protein Constructs: Aggregation of Fc- and HSA- Based Fusion Proteins. [Internet] [Doctoral dissertation]. University of Colorado; 2011. [cited 2020 Jul 08]. Available from: https://scholar.colorado.edu/chbe_gradetds/20.

Council of Science Editors:

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


University of Colorado

2. Sorret, Lea Line Gisele. The Role of Protein-Protein Interactions in Inducing Interfacial Aggregation.

Degree: PhD, 2018, University of Colorado

  The synergic exposure to silicone oil-water interfaces and to agitation has been shown to promote the aggregation of therapeutic proteins. Silicone oil is typically… (more)

Subjects/Keywords: adsorption; interfaces; protein aggregation; protein stability; rheology; Biological Engineering; Chemical Engineering

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APA (6th Edition):

Sorret, L. L. G. (2018). The Role of Protein-Protein Interactions in Inducing Interfacial Aggregation. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/117

Chicago Manual of Style (16th Edition):

Sorret, Lea Line Gisele. “The Role of Protein-Protein Interactions in Inducing Interfacial Aggregation.” 2018. Doctoral Dissertation, University of Colorado. Accessed July 08, 2020. https://scholar.colorado.edu/chbe_gradetds/117.

MLA Handbook (7th Edition):

Sorret, Lea Line Gisele. “The Role of Protein-Protein Interactions in Inducing Interfacial Aggregation.” 2018. Web. 08 Jul 2020.

Vancouver:

Sorret LLG. The Role of Protein-Protein Interactions in Inducing Interfacial Aggregation. [Internet] [Doctoral dissertation]. University of Colorado; 2018. [cited 2020 Jul 08]. Available from: https://scholar.colorado.edu/chbe_gradetds/117.

Council of Science Editors:

Sorret LLG. The Role of Protein-Protein Interactions in Inducing Interfacial Aggregation. [Doctoral Dissertation]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/chbe_gradetds/117


University of Colorado

3. 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 08, 2020. https://scholar.colorado.edu/chbe_gradetds/89.

MLA Handbook (7th Edition):

Nordwald, Erik Michael. “Engineering ionic liquid tolerant enzymes.” 2015. Web. 08 Jul 2020.

Vancouver:

Nordwald EM. Engineering ionic liquid tolerant enzymes. [Internet] [Doctoral dissertation]. University of Colorado; 2015. [cited 2020 Jul 08]. 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


University of Colorado

4. Wu, Hsin-Jui. Microfluidic Devices for Membrane Protein Nanoparticle Formation.

Degree: PhD, Mechanical Engineering, 2013, University of Colorado

  Microfluidic devices, so-called BioMEMs, or Lab on a chip, have been widely used to improve the science and technology, especially in biological applications. The… (more)

Subjects/Keywords: BioMEMS; Crystallization; Lab on a chip; Membrane protein; Microfluidic device; reconstitution; Biomechanical Engineering; Mechanical Engineering

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APA (6th Edition):

Wu, H. (2013). Microfluidic Devices for Membrane Protein Nanoparticle Formation. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcen_gradetds/57

Chicago Manual of Style (16th Edition):

Wu, Hsin-Jui. “Microfluidic Devices for Membrane Protein Nanoparticle Formation.” 2013. Doctoral Dissertation, University of Colorado. Accessed July 08, 2020. https://scholar.colorado.edu/mcen_gradetds/57.

MLA Handbook (7th Edition):

Wu, Hsin-Jui. “Microfluidic Devices for Membrane Protein Nanoparticle Formation.” 2013. Web. 08 Jul 2020.

Vancouver:

Wu H. Microfluidic Devices for Membrane Protein Nanoparticle Formation. [Internet] [Doctoral dissertation]. University of Colorado; 2013. [cited 2020 Jul 08]. Available from: https://scholar.colorado.edu/mcen_gradetds/57.

Council of Science Editors:

Wu H. Microfluidic Devices for Membrane Protein Nanoparticle Formation. [Doctoral Dissertation]. University of Colorado; 2013. Available from: https://scholar.colorado.edu/mcen_gradetds/57


University of Colorado

5. Chisholm, Carly Fleagle. The Immunogenicity of Therapeutic Protein Formulations Containing Silicone Oil Microdroplets.

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

  Subvisible particles in therapeutic protein products may act as adjuvants to provoke unwanted immune responses against administered proteins. Silicone oil is used as a… (more)

Subjects/Keywords: adjuvant effect; protein aggregation; Biomedical Engineering and Bioengineering; Chemical Engineering; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Chisholm, C. F. (2015). The Immunogenicity of Therapeutic Protein Formulations Containing Silicone Oil Microdroplets. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/90

Chicago Manual of Style (16th Edition):

Chisholm, Carly Fleagle. “The Immunogenicity of Therapeutic Protein Formulations Containing Silicone Oil Microdroplets.” 2015. Doctoral Dissertation, University of Colorado. Accessed July 08, 2020. https://scholar.colorado.edu/chbe_gradetds/90.

MLA Handbook (7th Edition):

Chisholm, Carly Fleagle. “The Immunogenicity of Therapeutic Protein Formulations Containing Silicone Oil Microdroplets.” 2015. Web. 08 Jul 2020.

Vancouver:

Chisholm CF. The Immunogenicity of Therapeutic Protein Formulations Containing Silicone Oil Microdroplets. [Internet] [Doctoral dissertation]. University of Colorado; 2015. [cited 2020 Jul 08]. Available from: https://scholar.colorado.edu/chbe_gradetds/90.

Council of Science Editors:

Chisholm CF. The Immunogenicity of Therapeutic Protein Formulations Containing Silicone Oil Microdroplets. [Doctoral Dissertation]. University of Colorado; 2015. Available from: https://scholar.colorado.edu/chbe_gradetds/90


University of Colorado

6. Plaks, Joseph Gabriel. Computational Protein Design for Peptide-Directed Bioconjugation.

Degree: PhD, 2019, University of Colorado

  Proteins enable living organisms to perform many of their critical functions, having been applied over evolutionary time to solve problems of overwhelming diversity and… (more)

Subjects/Keywords: bioconjugation; click chemistry; lipoic acid ligase; protein engineering; quorum sensing; rosetta; Biochemistry; Biomedical Engineering and Bioengineering; Materials Science and Engineering

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APA (6th Edition):

Plaks, J. G. (2019). Computational Protein Design for Peptide-Directed Bioconjugation. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/140

Chicago Manual of Style (16th Edition):

Plaks, Joseph Gabriel. “Computational Protein Design for Peptide-Directed Bioconjugation.” 2019. Doctoral Dissertation, University of Colorado. Accessed July 08, 2020. https://scholar.colorado.edu/chbe_gradetds/140.

MLA Handbook (7th Edition):

Plaks, Joseph Gabriel. “Computational Protein Design for Peptide-Directed Bioconjugation.” 2019. Web. 08 Jul 2020.

Vancouver:

Plaks JG. Computational Protein Design for Peptide-Directed Bioconjugation. [Internet] [Doctoral dissertation]. University of Colorado; 2019. [cited 2020 Jul 08]. Available from: https://scholar.colorado.edu/chbe_gradetds/140.

Council of Science Editors:

Plaks JG. Computational Protein Design for Peptide-Directed Bioconjugation. [Doctoral Dissertation]. University of Colorado; 2019. Available from: https://scholar.colorado.edu/chbe_gradetds/140


University of Colorado

7. McCall, Joshua Daniel. Poly(ethylene glycol) based biomaterial platforms for guiding cell behavior through control of presentation and release of bioactive, therapeutic proteins.

Degree: PhD, Chemical & Biochemical Engineering, 2012, University of Colorado

  Poly(ethylene glycol) (PEG) based biomaterials offer a number of advantages for applications in biomedical technology, including drug delivery and tissue engineering. PEG is notable… (more)

Subjects/Keywords: biomaterial; Hydrogel; immobilized growth factor; Protein delivery; stem cell differentiation; Tissue Engineering; Biomedical Engineering and Bioengineering; Chemical Engineering; Polymer Science

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APA (6th Edition):

McCall, J. D. (2012). Poly(ethylene glycol) based biomaterial platforms for guiding cell behavior through control of presentation and release of bioactive, therapeutic proteins. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/26

Chicago Manual of Style (16th Edition):

McCall, Joshua Daniel. “Poly(ethylene glycol) based biomaterial platforms for guiding cell behavior through control of presentation and release of bioactive, therapeutic proteins.” 2012. Doctoral Dissertation, University of Colorado. Accessed July 08, 2020. https://scholar.colorado.edu/chbe_gradetds/26.

MLA Handbook (7th Edition):

McCall, Joshua Daniel. “Poly(ethylene glycol) based biomaterial platforms for guiding cell behavior through control of presentation and release of bioactive, therapeutic proteins.” 2012. Web. 08 Jul 2020.

Vancouver:

McCall JD. Poly(ethylene glycol) based biomaterial platforms for guiding cell behavior through control of presentation and release of bioactive, therapeutic proteins. [Internet] [Doctoral dissertation]. University of Colorado; 2012. [cited 2020 Jul 08]. Available from: https://scholar.colorado.edu/chbe_gradetds/26.

Council of Science Editors:

McCall JD. Poly(ethylene glycol) based biomaterial platforms for guiding cell behavior through control of presentation and release of bioactive, therapeutic proteins. [Doctoral Dissertation]. University of Colorado; 2012. Available from: https://scholar.colorado.edu/chbe_gradetds/26


University of Colorado

8. Carter, Kyle Pierce. Engineering and Evaluating Fluorescent Tools for Endoplasmic Reticulum Zinc.

Degree: PhD, Chemistry & Biochemistry, 2017, University of Colorado

 Zinc (Zn2+) is an essential micronutrient for human health. However, excess Zn2+ is toxic and Zn2+ deficiency can be fatal, so the concentration of this… (more)

Subjects/Keywords: Biosensors; Endoplasmic reticulum; Fluorescence microscopy; FRET; Protein engineering; Zinc; Biochemistry; Biophysics; Cell Biology

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APA (6th Edition):

Carter, K. P. (2017). Engineering and Evaluating Fluorescent Tools for Endoplasmic Reticulum Zinc. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/223

Chicago Manual of Style (16th Edition):

Carter, Kyle Pierce. “Engineering and Evaluating Fluorescent Tools for Endoplasmic Reticulum Zinc.” 2017. Doctoral Dissertation, University of Colorado. Accessed July 08, 2020. https://scholar.colorado.edu/chem_gradetds/223.

MLA Handbook (7th Edition):

Carter, Kyle Pierce. “Engineering and Evaluating Fluorescent Tools for Endoplasmic Reticulum Zinc.” 2017. Web. 08 Jul 2020.

Vancouver:

Carter KP. Engineering and Evaluating Fluorescent Tools for Endoplasmic Reticulum Zinc. [Internet] [Doctoral dissertation]. University of Colorado; 2017. [cited 2020 Jul 08]. Available from: https://scholar.colorado.edu/chem_gradetds/223.

Council of Science Editors:

Carter KP. Engineering and Evaluating Fluorescent Tools for Endoplasmic Reticulum Zinc. [Doctoral Dissertation]. University of Colorado; 2017. Available from: https://scholar.colorado.edu/chem_gradetds/223


University of Colorado

9. McUmber, Aaron Christopher. Understanding How Non-Covalent Interactions Affect Interfacial Biomolecular Dynamics.

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

  Biopolymers, such as proteins and nucleic acids, are omnipresent in modern applications. The need to control interfacial molecular systems is becoming increasingly important in… (more)

Subjects/Keywords: Aggregation; Interface; Nucleic Acid; Protein; Single Molecule; TIRFM; Biochemical and Biomolecular Engineering

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APA (6th Edition):

McUmber, A. C. (2015). Understanding How Non-Covalent Interactions Affect Interfacial Biomolecular Dynamics. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/88

Chicago Manual of Style (16th Edition):

McUmber, Aaron Christopher. “Understanding How Non-Covalent Interactions Affect Interfacial Biomolecular Dynamics.” 2015. Doctoral Dissertation, University of Colorado. Accessed July 08, 2020. https://scholar.colorado.edu/chbe_gradetds/88.

MLA Handbook (7th Edition):

McUmber, Aaron Christopher. “Understanding How Non-Covalent Interactions Affect Interfacial Biomolecular Dynamics.” 2015. Web. 08 Jul 2020.

Vancouver:

McUmber AC. Understanding How Non-Covalent Interactions Affect Interfacial Biomolecular Dynamics. [Internet] [Doctoral dissertation]. University of Colorado; 2015. [cited 2020 Jul 08]. Available from: https://scholar.colorado.edu/chbe_gradetds/88.

Council of Science Editors:

McUmber AC. Understanding How Non-Covalent Interactions Affect Interfacial Biomolecular Dynamics. [Doctoral Dissertation]. University of Colorado; 2015. Available from: https://scholar.colorado.edu/chbe_gradetds/88


University of Colorado

10. Faulon Marruecos, David. Connecting Protein Structure and Dynamics on Biomaterials with the Foreign Body Response.

Degree: PhD, 2018, University of Colorado

  The harsh environment of the foreign body response (FBR) has the potential to negatively impact the implantations of biomaterials in the body. The FBR… (more)

Subjects/Keywords: fibronectin; fluorescence microscopy; fret; polymer brushes; protein structure; single molecule; Biomedical Engineering and Bioengineering; Biophysics; Chemical Engineering

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APA (6th Edition):

Faulon Marruecos, D. (2018). Connecting Protein Structure and Dynamics on Biomaterials with the Foreign Body Response. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/132

Chicago Manual of Style (16th Edition):

Faulon Marruecos, David. “Connecting Protein Structure and Dynamics on Biomaterials with the Foreign Body Response.” 2018. Doctoral Dissertation, University of Colorado. Accessed July 08, 2020. https://scholar.colorado.edu/chbe_gradetds/132.

MLA Handbook (7th Edition):

Faulon Marruecos, David. “Connecting Protein Structure and Dynamics on Biomaterials with the Foreign Body Response.” 2018. Web. 08 Jul 2020.

Vancouver:

Faulon Marruecos D. Connecting Protein Structure and Dynamics on Biomaterials with the Foreign Body Response. [Internet] [Doctoral dissertation]. University of Colorado; 2018. [cited 2020 Jul 08]. Available from: https://scholar.colorado.edu/chbe_gradetds/132.

Council of Science Editors:

Faulon Marruecos D. Connecting Protein Structure and Dynamics on Biomaterials with the Foreign Body Response. [Doctoral Dissertation]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/chbe_gradetds/132


University of Colorado

11. Manna, Premashis. Development and Characterization of Improved Red Fluorescent Protein Variants.

Degree: PhD, Chemistry & Biochemistry, 2018, University of Colorado

  Aequorea victoria-based green fluorescent proteins and their blue, cyan and red counterparts offer unprecedented advantage as biological markers owing to their genetic encodability and… (more)

Subjects/Keywords: directed evolution; excited state lifetime; microfluidics; protein engineering; radiative lifetime; red fluorescent proteins; Biomedical Engineering and Bioengineering; Biophysics; Physical Chemistry

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APA (6th Edition):

Manna, P. (2018). Development and Characterization of Improved Red Fluorescent Protein Variants. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/238

Chicago Manual of Style (16th Edition):

Manna, Premashis. “Development and Characterization of Improved Red Fluorescent Protein Variants.” 2018. Doctoral Dissertation, University of Colorado. Accessed July 08, 2020. https://scholar.colorado.edu/chem_gradetds/238.

MLA Handbook (7th Edition):

Manna, Premashis. “Development and Characterization of Improved Red Fluorescent Protein Variants.” 2018. Web. 08 Jul 2020.

Vancouver:

Manna P. Development and Characterization of Improved Red Fluorescent Protein Variants. [Internet] [Doctoral dissertation]. University of Colorado; 2018. [cited 2020 Jul 08]. Available from: https://scholar.colorado.edu/chem_gradetds/238.

Council of Science Editors:

Manna P. Development and Characterization of Improved Red Fluorescent Protein Variants. [Doctoral Dissertation]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/chem_gradetds/238


University of Colorado

12. Langdon, Blake Brianna. Real-time single-molecule observations of proteins at the solid-liquid interface.

Degree: PhD, Chemical & Biochemical Engineering, 2014, University of Colorado

  Non-specific protein adsorption to solid surfaces is pervasive and observed across a broad spectrum of applications including biomaterials, separations, pharmaceuticals, and biosensing. Despite great… (more)

Subjects/Keywords: protein adsorption; protein aggregation; solid-liquid interface; surface hydrophobicity; total internal reflection fluorescence microscopy; Biomedical Engineering and Bioengineering; Biophysics; Nanoscience and Nanotechnology

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APA (6th Edition):

Langdon, B. B. (2014). Real-time single-molecule observations of proteins at the solid-liquid interface. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/71

Chicago Manual of Style (16th Edition):

Langdon, Blake Brianna. “Real-time single-molecule observations of proteins at the solid-liquid interface.” 2014. Doctoral Dissertation, University of Colorado. Accessed July 08, 2020. https://scholar.colorado.edu/chbe_gradetds/71.

MLA Handbook (7th Edition):

Langdon, Blake Brianna. “Real-time single-molecule observations of proteins at the solid-liquid interface.” 2014. Web. 08 Jul 2020.

Vancouver:

Langdon BB. Real-time single-molecule observations of proteins at the solid-liquid interface. [Internet] [Doctoral dissertation]. University of Colorado; 2014. [cited 2020 Jul 08]. Available from: https://scholar.colorado.edu/chbe_gradetds/71.

Council of Science Editors:

Langdon BB. Real-time single-molecule observations of proteins at the solid-liquid interface. [Doctoral Dissertation]. University of Colorado; 2014. Available from: https://scholar.colorado.edu/chbe_gradetds/71


University of Colorado

13. Gadek, Katherine Elise. Skeletal Muscle Metabolism: from Tissue to Stem Cell.

Degree: PhD, 2018, University of Colorado

  Excessive circulating triglycerides due to reduction or loss of lipoprotein lipase (LPL) activity contribute to hypertriglyceridemia and increased risk for pancreatitis. The only gene… (more)

Subjects/Keywords: metabolism; molecular clock; muscle; rna binding protein; stem cells; Molecular Biology; Molecular, Cellular, and Tissue Engineering

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APA (6th Edition):

Gadek, K. E. (2018). Skeletal Muscle Metabolism: from Tissue to Stem Cell. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/82

Chicago Manual of Style (16th Edition):

Gadek, Katherine Elise. “Skeletal Muscle Metabolism: from Tissue to Stem Cell.” 2018. Doctoral Dissertation, University of Colorado. Accessed July 08, 2020. https://scholar.colorado.edu/mcdb_gradetds/82.

MLA Handbook (7th Edition):

Gadek, Katherine Elise. “Skeletal Muscle Metabolism: from Tissue to Stem Cell.” 2018. Web. 08 Jul 2020.

Vancouver:

Gadek KE. Skeletal Muscle Metabolism: from Tissue to Stem Cell. [Internet] [Doctoral dissertation]. University of Colorado; 2018. [cited 2020 Jul 08]. Available from: https://scholar.colorado.edu/mcdb_gradetds/82.

Council of Science Editors:

Gadek KE. Skeletal Muscle Metabolism: from Tissue to Stem Cell. [Doctoral Dissertation]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/mcdb_gradetds/82


University of Colorado

14. Bordoy, Antoni Escalas. Modeling and Designing Genetic Devices Using Transcriptional Interference in Escherichia Coli.

Degree: PhD, 2018, University of Colorado

 Microorganisms inhabit every extreme location of our planet. In their journey through the ages, they have been able to incredibly adapt to a myriad of… (more)

Subjects/Keywords: genetic logic gates; mathematical modeling; protein feedback; rna interaction; synthetic biology; transcriptional interference; Biomedical Engineering and Bioengineering; Genetics; Molecular Biology

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APA (6th Edition):

Bordoy, A. E. (2018). Modeling and Designing Genetic Devices Using Transcriptional Interference in Escherichia Coli. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/129

Chicago Manual of Style (16th Edition):

Bordoy, Antoni Escalas. “Modeling and Designing Genetic Devices Using Transcriptional Interference in Escherichia Coli.” 2018. Doctoral Dissertation, University of Colorado. Accessed July 08, 2020. https://scholar.colorado.edu/chbe_gradetds/129.

MLA Handbook (7th Edition):

Bordoy, Antoni Escalas. “Modeling and Designing Genetic Devices Using Transcriptional Interference in Escherichia Coli.” 2018. Web. 08 Jul 2020.

Vancouver:

Bordoy AE. Modeling and Designing Genetic Devices Using Transcriptional Interference in Escherichia Coli. [Internet] [Doctoral dissertation]. University of Colorado; 2018. [cited 2020 Jul 08]. Available from: https://scholar.colorado.edu/chbe_gradetds/129.

Council of Science Editors:

Bordoy AE. Modeling and Designing Genetic Devices Using Transcriptional Interference in Escherichia Coli. [Doctoral Dissertation]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/chbe_gradetds/129


University of Colorado

15. Poepping, Christopher. Medium-Pressure UV Disinfection: Evaluation of Unintended DNA Damage Reversal and Adenoviral Protein Damage Using Wavelength Specific Irradiation.

Degree: MS, 2013, University of Colorado

  Medium-pressure (MP) ultraviolet (UV) lamps are becoming a popular technology for UV disinfection. They have demonstrated significant advantages over conventional low-pressure (LP) UV lamps… (more)

Subjects/Keywords: adenovirus; cyclobutane pyrimidine dimer; dna damage reversal; medium-pressure; protein damage; uv disinfection; Biology; Civil and Environmental Engineering

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APA (6th Edition):

Poepping, C. (2013). Medium-Pressure UV Disinfection: Evaluation of Unintended DNA Damage Reversal and Adenoviral Protein Damage Using Wavelength Specific Irradiation. (Masters Thesis). University of Colorado. Retrieved from https://scholar.colorado.edu/cven_gradetds/453

Chicago Manual of Style (16th Edition):

Poepping, Christopher. “Medium-Pressure UV Disinfection: Evaluation of Unintended DNA Damage Reversal and Adenoviral Protein Damage Using Wavelength Specific Irradiation.” 2013. Masters Thesis, University of Colorado. Accessed July 08, 2020. https://scholar.colorado.edu/cven_gradetds/453.

MLA Handbook (7th Edition):

Poepping, Christopher. “Medium-Pressure UV Disinfection: Evaluation of Unintended DNA Damage Reversal and Adenoviral Protein Damage Using Wavelength Specific Irradiation.” 2013. Web. 08 Jul 2020.

Vancouver:

Poepping C. Medium-Pressure UV Disinfection: Evaluation of Unintended DNA Damage Reversal and Adenoviral Protein Damage Using Wavelength Specific Irradiation. [Internet] [Masters thesis]. University of Colorado; 2013. [cited 2020 Jul 08]. Available from: https://scholar.colorado.edu/cven_gradetds/453.

Council of Science Editors:

Poepping C. Medium-Pressure UV Disinfection: Evaluation of Unintended DNA Damage Reversal and Adenoviral Protein Damage Using Wavelength Specific Irradiation. [Masters Thesis]. University of Colorado; 2013. Available from: https://scholar.colorado.edu/cven_gradetds/453


University of Colorado

16. Shomali, Maliheh. Immunogenicity of Therapeutic Proteins: Antibody Responses in Mice to Particulates Formed by Adsorbing a Murine Monoclonal Antibody onto Microparticles.

Degree: PhD, Chemical & Biochemical Engineering, 2013, University of Colorado

  The immunogenic potential of therapeutic proteins has been known for over half a century. However, there is still a debate about the factors that… (more)

Subjects/Keywords: Aggregates; Anti-drug antibody; ELISA; Immunogenicity; Low/hign zone tolerance; Protein; Chemical Engineering; Immunology and Infectious Disease

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APA (6th Edition):

Shomali, M. (2013). Immunogenicity of Therapeutic Proteins: Antibody Responses in Mice to Particulates Formed by Adsorbing a Murine Monoclonal Antibody onto Microparticles. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/39

Chicago Manual of Style (16th Edition):

Shomali, Maliheh. “Immunogenicity of Therapeutic Proteins: Antibody Responses in Mice to Particulates Formed by Adsorbing a Murine Monoclonal Antibody onto Microparticles.” 2013. Doctoral Dissertation, University of Colorado. Accessed July 08, 2020. https://scholar.colorado.edu/chbe_gradetds/39.

MLA Handbook (7th Edition):

Shomali, Maliheh. “Immunogenicity of Therapeutic Proteins: Antibody Responses in Mice to Particulates Formed by Adsorbing a Murine Monoclonal Antibody onto Microparticles.” 2013. Web. 08 Jul 2020.

Vancouver:

Shomali M. Immunogenicity of Therapeutic Proteins: Antibody Responses in Mice to Particulates Formed by Adsorbing a Murine Monoclonal Antibody onto Microparticles. [Internet] [Doctoral dissertation]. University of Colorado; 2013. [cited 2020 Jul 08]. Available from: https://scholar.colorado.edu/chbe_gradetds/39.

Council of Science Editors:

Shomali M. Immunogenicity of Therapeutic Proteins: Antibody Responses in Mice to Particulates Formed by Adsorbing a Murine Monoclonal Antibody onto Microparticles. [Doctoral Dissertation]. University of Colorado; 2013. Available from: https://scholar.colorado.edu/chbe_gradetds/39


University of Colorado

17. Gerhardt, Alana. Synergistic Effects of Interfaces and Agitation on Particle Formation in Therapeutic Protein Formulations in Pre-filled Syringes.

Degree: PhD, 2014, University of Colorado

  Pre-filled syringes are commonly used storage and delivery devices for protein therapeutics because of their convenience and ease of use. However, in a pre-filled… (more)

Subjects/Keywords: monoclonal antibody; particle formation; pre-filled syringes; protein aggregation; silicone oil; Biochemical and Biomolecular Engineering; Medicinal Chemistry and Pharmaceutics

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APA (6th Edition):

Gerhardt, A. (2014). Synergistic Effects of Interfaces and Agitation on Particle Formation in Therapeutic Protein Formulations in Pre-filled Syringes. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/60

Chicago Manual of Style (16th Edition):

Gerhardt, Alana. “Synergistic Effects of Interfaces and Agitation on Particle Formation in Therapeutic Protein Formulations in Pre-filled Syringes.” 2014. Doctoral Dissertation, University of Colorado. Accessed July 08, 2020. https://scholar.colorado.edu/chbe_gradetds/60.

MLA Handbook (7th Edition):

Gerhardt, Alana. “Synergistic Effects of Interfaces and Agitation on Particle Formation in Therapeutic Protein Formulations in Pre-filled Syringes.” 2014. Web. 08 Jul 2020.

Vancouver:

Gerhardt A. Synergistic Effects of Interfaces and Agitation on Particle Formation in Therapeutic Protein Formulations in Pre-filled Syringes. [Internet] [Doctoral dissertation]. University of Colorado; 2014. [cited 2020 Jul 08]. Available from: https://scholar.colorado.edu/chbe_gradetds/60.

Council of Science Editors:

Gerhardt A. Synergistic Effects of Interfaces and Agitation on Particle Formation in Therapeutic Protein Formulations in Pre-filled Syringes. [Doctoral Dissertation]. University of Colorado; 2014. Available from: https://scholar.colorado.edu/chbe_gradetds/60


University of Colorado

18. Russell, Elisabeth Emily. Monoclonal Antibody Aggregation in Cell Culture: Aggregate Characterization and Protein Stability Analysis.

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

Protein aggregates represent a safety, immunological and stability concern in therapeutic protein formulations. Aggregates may be formed at any stage during the manufacturing process,… (more)

Subjects/Keywords: aggregation; monoclonal antibody; protein; therapeutic; Amino Acids, Peptides, and Proteins; Biochemical and Biomolecular Engineering; Pharmaceutical Preparations

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

APA (6th Edition):

Russell, E. E. (2015). Monoclonal Antibody Aggregation in Cell Culture: Aggregate Characterization and Protein Stability Analysis. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/85

Chicago Manual of Style (16th Edition):

Russell, Elisabeth Emily. “Monoclonal Antibody Aggregation in Cell Culture: Aggregate Characterization and Protein Stability Analysis.” 2015. Doctoral Dissertation, University of Colorado. Accessed July 08, 2020. https://scholar.colorado.edu/chbe_gradetds/85.

MLA Handbook (7th Edition):

Russell, Elisabeth Emily. “Monoclonal Antibody Aggregation in Cell Culture: Aggregate Characterization and Protein Stability Analysis.” 2015. Web. 08 Jul 2020.

Vancouver:

Russell EE. Monoclonal Antibody Aggregation in Cell Culture: Aggregate Characterization and Protein Stability Analysis. [Internet] [Doctoral dissertation]. University of Colorado; 2015. [cited 2020 Jul 08]. Available from: https://scholar.colorado.edu/chbe_gradetds/85.

Council of Science Editors:

Russell EE. Monoclonal Antibody Aggregation in Cell Culture: Aggregate Characterization and Protein Stability Analysis. [Doctoral Dissertation]. University of Colorado; 2015. Available from: https://scholar.colorado.edu/chbe_gradetds/85

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