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Dates: Last 2 Years

You searched for subject:(Protein chemistry). Showing records 1 – 30 of 103 total matches.

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University of Michigan

1. Clark, Jordan. Structural Investigation of Binding Events in Proteins.

Degree: PhD, Medicinal Chemistry, 2018, University of Michigan

 Understanding the biophysical properties that describe protein binding events has allowed for the advancement of drug discovery through structure-based drug design and in silico methodology.… (more)

Subjects/Keywords: Protein flexibility; Protein structure database; Protein-ligand binding; Protein-protein interaction (PPI); Biological Chemistry; Science

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APA (6th Edition):

Clark, J. (2018). Structural Investigation of Binding Events in Proteins. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/145943

Chicago Manual of Style (16th Edition):

Clark, Jordan. “Structural Investigation of Binding Events in Proteins.” 2018. Doctoral Dissertation, University of Michigan. Accessed June 19, 2019. http://hdl.handle.net/2027.42/145943.

MLA Handbook (7th Edition):

Clark, Jordan. “Structural Investigation of Binding Events in Proteins.” 2018. Web. 19 Jun 2019.

Vancouver:

Clark J. Structural Investigation of Binding Events in Proteins. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/2027.42/145943.

Council of Science Editors:

Clark J. Structural Investigation of Binding Events in Proteins. [Doctoral Dissertation]. University of Michigan; 2018. Available from: http://hdl.handle.net/2027.42/145943


Cornell University

2. Wan, Huahua. Finding A Volume Ratio of Hyaluronic Acid to Phe-Arg-Poly(ester amide)s to Form Drug-Delivering Nanoparticle Micelles and Preliminary Drug Loading Result .

Degree: 2018, Cornell University

 Pseudo-protein is a name used to describe an amino acid based poly(ester amide)s (aa-PEA). One possible application of pseudo-protein is as a drug delivery coating.To… (more)

Subjects/Keywords: Pseudo-protein; nanoparticle; Chemistry

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APA (6th Edition):

Wan, H. (2018). Finding A Volume Ratio of Hyaluronic Acid to Phe-Arg-Poly(ester amide)s to Form Drug-Delivering Nanoparticle Micelles and Preliminary Drug Loading Result . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/64991

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):

Wan, Huahua. “Finding A Volume Ratio of Hyaluronic Acid to Phe-Arg-Poly(ester amide)s to Form Drug-Delivering Nanoparticle Micelles and Preliminary Drug Loading Result .” 2018. Thesis, Cornell University. Accessed June 19, 2019. http://hdl.handle.net/1813/64991.

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

MLA Handbook (7th Edition):

Wan, Huahua. “Finding A Volume Ratio of Hyaluronic Acid to Phe-Arg-Poly(ester amide)s to Form Drug-Delivering Nanoparticle Micelles and Preliminary Drug Loading Result .” 2018. Web. 19 Jun 2019.

Vancouver:

Wan H. Finding A Volume Ratio of Hyaluronic Acid to Phe-Arg-Poly(ester amide)s to Form Drug-Delivering Nanoparticle Micelles and Preliminary Drug Loading Result . [Internet] [Thesis]. Cornell University; 2018. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/1813/64991.

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

Council of Science Editors:

Wan H. Finding A Volume Ratio of Hyaluronic Acid to Phe-Arg-Poly(ester amide)s to Form Drug-Delivering Nanoparticle Micelles and Preliminary Drug Loading Result . [Thesis]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/64991

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


University of California – San Diego

3. Maniaci, Brian M. Design of Metal-Controlled Protein-Protein Interactions.

Degree: Chemistry and Biochemistry, 2019, University of California – San Diego

 The field of protein design strives to engineer new molecules that interact in a specific, controlled manner to form novel functional complexes. Engineered proteins that… (more)

Subjects/Keywords: Chemistry; Biochemistry; Biomaterials; Metal-Controlled Protein Dimerization; Protein Design; Protein Engineering

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

APA (6th Edition):

Maniaci, B. M. (2019). Design of Metal-Controlled Protein-Protein Interactions. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/0fc2n3qm

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

Chicago Manual of Style (16th Edition):

Maniaci, Brian M. “Design of Metal-Controlled Protein-Protein Interactions.” 2019. Thesis, University of California – San Diego. Accessed June 19, 2019. http://www.escholarship.org/uc/item/0fc2n3qm.

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

MLA Handbook (7th Edition):

Maniaci, Brian M. “Design of Metal-Controlled Protein-Protein Interactions.” 2019. Web. 19 Jun 2019.

Vancouver:

Maniaci BM. Design of Metal-Controlled Protein-Protein Interactions. [Internet] [Thesis]. University of California – San Diego; 2019. [cited 2019 Jun 19]. Available from: http://www.escholarship.org/uc/item/0fc2n3qm.

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

Council of Science Editors:

Maniaci BM. Design of Metal-Controlled Protein-Protein Interactions. [Thesis]. University of California – San Diego; 2019. Available from: http://www.escholarship.org/uc/item/0fc2n3qm

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


University of Washington

4. Anderson, Jordan Micheal. Caps - Turns - Loops: Designing Better β-Hairpins.

Degree: PhD, 2017, University of Washington

 As protein engineering promises advances in almost every field of science and medicine, a greater understanding of the protein folding problem is necessary to make… (more)

Subjects/Keywords: NMR; Peptide; Protein Design; Protein Folding; β-Hairpin; β-Sheet; Chemistry; Biochemistry; Organic chemistry; Chemistry

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APA (6th Edition):

Anderson, J. M. (2017). Caps - Turns - Loops: Designing Better β-Hairpins. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/40518

Chicago Manual of Style (16th Edition):

Anderson, Jordan Micheal. “Caps - Turns - Loops: Designing Better β-Hairpins.” 2017. Doctoral Dissertation, University of Washington. Accessed June 19, 2019. http://hdl.handle.net/1773/40518.

MLA Handbook (7th Edition):

Anderson, Jordan Micheal. “Caps - Turns - Loops: Designing Better β-Hairpins.” 2017. Web. 19 Jun 2019.

Vancouver:

Anderson JM. Caps - Turns - Loops: Designing Better β-Hairpins. [Internet] [Doctoral dissertation]. University of Washington; 2017. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/1773/40518.

Council of Science Editors:

Anderson JM. Caps - Turns - Loops: Designing Better β-Hairpins. [Doctoral Dissertation]. University of Washington; 2017. Available from: http://hdl.handle.net/1773/40518


University of Vienna

5. Pellikan, Sarala. Identification and quantification of peptides via HPLC and MS.

Degree: 2018, University of Vienna

In dieser Studie zeigen wir, dass Aminosäuren unter verschiedenen pH-Bedingungen aufgetrennt werden können und führen sie als Vorstudie für Rinderserumalbumin durch. Im praktischen Teil wurden… (more)

Subjects/Keywords: 44.40 Pharmazie, Pharmazeutika; 44.42 Pharmazeutische Chemie; BSA / HPLC / MS / Protein / Tryptophan; BSA / HPLC / MS / Protein / Tryptophan

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APA (6th Edition):

Pellikan, S. (2018). Identification and quantification of peptides via HPLC and MS. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/52774/

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):

Pellikan, Sarala. “Identification and quantification of peptides via HPLC and MS.” 2018. Thesis, University of Vienna. Accessed June 19, 2019. http://othes.univie.ac.at/52774/.

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

MLA Handbook (7th Edition):

Pellikan, Sarala. “Identification and quantification of peptides via HPLC and MS.” 2018. Web. 19 Jun 2019.

Vancouver:

Pellikan S. Identification and quantification of peptides via HPLC and MS. [Internet] [Thesis]. University of Vienna; 2018. [cited 2019 Jun 19]. Available from: http://othes.univie.ac.at/52774/.

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

Council of Science Editors:

Pellikan S. Identification and quantification of peptides via HPLC and MS. [Thesis]. University of Vienna; 2018. Available from: http://othes.univie.ac.at/52774/

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


University of California – San Diego

6. Xu, Zhenzhu. Protein Adsorption on Metal Oxide Nanoparticle Surfaces: Effects of Various Influences on Protein-Surface Interactions and Protein Structure.

Degree: Chemistry, 2018, University of California – San Diego

 With the development of nanoscience and nanotechnology, the biocompatibility of nanomaterials is becoming increasingly important. As one of the most prevalent nanomaterials, metal oxide nanoparticles… (more)

Subjects/Keywords: Chemistry; ATR-FTIR; nanoparticles; nanotechnology; protein adsorption; protein corona; protein-surface interactions

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APA (6th Edition):

Xu, Z. (2018). Protein Adsorption on Metal Oxide Nanoparticle Surfaces: Effects of Various Influences on Protein-Surface Interactions and Protein Structure. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/9425f20d

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):

Xu, Zhenzhu. “Protein Adsorption on Metal Oxide Nanoparticle Surfaces: Effects of Various Influences on Protein-Surface Interactions and Protein Structure.” 2018. Thesis, University of California – San Diego. Accessed June 19, 2019. http://www.escholarship.org/uc/item/9425f20d.

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

MLA Handbook (7th Edition):

Xu, Zhenzhu. “Protein Adsorption on Metal Oxide Nanoparticle Surfaces: Effects of Various Influences on Protein-Surface Interactions and Protein Structure.” 2018. Web. 19 Jun 2019.

Vancouver:

Xu Z. Protein Adsorption on Metal Oxide Nanoparticle Surfaces: Effects of Various Influences on Protein-Surface Interactions and Protein Structure. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2019 Jun 19]. Available from: http://www.escholarship.org/uc/item/9425f20d.

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

Council of Science Editors:

Xu Z. Protein Adsorption on Metal Oxide Nanoparticle Surfaces: Effects of Various Influences on Protein-Surface Interactions and Protein Structure. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/9425f20d

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


University of California – San Diego

7. Churchfield, Lewis Anthony. Design and Characterization of an Allosteric Metalloprotein Assembly.

Degree: Chemistry, 2018, University of California – San Diego

 Proteins are one of the main building blocks of life. Among their numerous functions are roles as biocatalysts for essential chemical reactions, signaling agents that… (more)

Subjects/Keywords: Chemistry; Biochemistry; biology; chemical; engineering; protein

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APA (6th Edition):

Churchfield, L. A. (2018). Design and Characterization of an Allosteric Metalloprotein Assembly. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/1hb2p09c

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):

Churchfield, Lewis Anthony. “Design and Characterization of an Allosteric Metalloprotein Assembly.” 2018. Thesis, University of California – San Diego. Accessed June 19, 2019. http://www.escholarship.org/uc/item/1hb2p09c.

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

MLA Handbook (7th Edition):

Churchfield, Lewis Anthony. “Design and Characterization of an Allosteric Metalloprotein Assembly.” 2018. Web. 19 Jun 2019.

Vancouver:

Churchfield LA. Design and Characterization of an Allosteric Metalloprotein Assembly. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2019 Jun 19]. Available from: http://www.escholarship.org/uc/item/1hb2p09c.

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

Council of Science Editors:

Churchfield LA. Design and Characterization of an Allosteric Metalloprotein Assembly. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/1hb2p09c

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


University of California – Irvine

8. Prytkova, Vera Dmitrievna. Development of multiple conformation Monte Carlo method and its application to protein aggregation in cataract formation.

Degree: Chemistry, 2018, University of California – Irvine

 Realistic biological conditions are characterized by high concentrations of biomolecular solutes. Protein conformations and protein-protein interactions can be affected by crowding. The inclusion of a… (more)

Subjects/Keywords: Chemistry; cataract; Monte Carlo simulations; protein aggregation

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APA (6th Edition):

Prytkova, V. D. (2018). Development of multiple conformation Monte Carlo method and its application to protein aggregation in cataract formation. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/0w31j57h

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):

Prytkova, Vera Dmitrievna. “Development of multiple conformation Monte Carlo method and its application to protein aggregation in cataract formation.” 2018. Thesis, University of California – Irvine. Accessed June 19, 2019. http://www.escholarship.org/uc/item/0w31j57h.

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

MLA Handbook (7th Edition):

Prytkova, Vera Dmitrievna. “Development of multiple conformation Monte Carlo method and its application to protein aggregation in cataract formation.” 2018. Web. 19 Jun 2019.

Vancouver:

Prytkova VD. Development of multiple conformation Monte Carlo method and its application to protein aggregation in cataract formation. [Internet] [Thesis]. University of California – Irvine; 2018. [cited 2019 Jun 19]. Available from: http://www.escholarship.org/uc/item/0w31j57h.

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

Council of Science Editors:

Prytkova VD. Development of multiple conformation Monte Carlo method and its application to protein aggregation in cataract formation. [Thesis]. University of California – Irvine; 2018. Available from: http://www.escholarship.org/uc/item/0w31j57h

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


Utah State University

9. Moise, Gwendolyn. Investigations into Factors Affecting the WPD-Loop in the Protein Tyrosine Phosphatases YopH and PTP1B.

Degree: PhD, Chemistry and Biochemistry, 2018, Utah State University

  The research in this dissertation documents connections between the primary amino acid sequence of proteins, the dynamics of proteins, and their catalytic function. This… (more)

Subjects/Keywords: PTP; hydrolase; kenetics; protein; dynamics; Chemistry

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APA (6th Edition):

Moise, G. (2018). Investigations into Factors Affecting the WPD-Loop in the Protein Tyrosine Phosphatases YopH and PTP1B. (Doctoral Dissertation). Utah State University. Retrieved from https://digitalcommons.usu.edu/etd/7226

Chicago Manual of Style (16th Edition):

Moise, Gwendolyn. “Investigations into Factors Affecting the WPD-Loop in the Protein Tyrosine Phosphatases YopH and PTP1B.” 2018. Doctoral Dissertation, Utah State University. Accessed June 19, 2019. https://digitalcommons.usu.edu/etd/7226.

MLA Handbook (7th Edition):

Moise, Gwendolyn. “Investigations into Factors Affecting the WPD-Loop in the Protein Tyrosine Phosphatases YopH and PTP1B.” 2018. Web. 19 Jun 2019.

Vancouver:

Moise G. Investigations into Factors Affecting the WPD-Loop in the Protein Tyrosine Phosphatases YopH and PTP1B. [Internet] [Doctoral dissertation]. Utah State University; 2018. [cited 2019 Jun 19]. Available from: https://digitalcommons.usu.edu/etd/7226.

Council of Science Editors:

Moise G. Investigations into Factors Affecting the WPD-Loop in the Protein Tyrosine Phosphatases YopH and PTP1B. [Doctoral Dissertation]. Utah State University; 2018. Available from: https://digitalcommons.usu.edu/etd/7226


University of Colorado

10. Hu, Zhenyi. Small-Molecule Tlr8 Antagonists Via Structure-Based Rational Design.

Degree: PhD, 2018, University of Colorado

  Immune system plays a critical role in defense against various virus and bacteria, and it’s composed of innate immune system and adaptive immune system.… (more)

Subjects/Keywords: antagonists; autoimmunity; protein-protein interactions; rational design; tlr8; Biomedical; Chemistry

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APA (6th Edition):

Hu, Z. (2018). Small-Molecule Tlr8 Antagonists Via Structure-Based Rational Design. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/246

Chicago Manual of Style (16th Edition):

Hu, Zhenyi. “Small-Molecule Tlr8 Antagonists Via Structure-Based Rational Design.” 2018. Doctoral Dissertation, University of Colorado. Accessed June 19, 2019. https://scholar.colorado.edu/chem_gradetds/246.

MLA Handbook (7th Edition):

Hu, Zhenyi. “Small-Molecule Tlr8 Antagonists Via Structure-Based Rational Design.” 2018. Web. 19 Jun 2019.

Vancouver:

Hu Z. Small-Molecule Tlr8 Antagonists Via Structure-Based Rational Design. [Internet] [Doctoral dissertation]. University of Colorado; 2018. [cited 2019 Jun 19]. Available from: https://scholar.colorado.edu/chem_gradetds/246.

Council of Science Editors:

Hu Z. Small-Molecule Tlr8 Antagonists Via Structure-Based Rational Design. [Doctoral Dissertation]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/chem_gradetds/246


Columbia University

11. Xu, Fang. Resonance-energy-transfer-based fluorescence imaging and free energy perturbation calculation.

Degree: 2018, Columbia University

 This thesis focuses on an important aspect of protein functionality – protein-protein interactions (PPI). Three physical chemistry techniques for or derived from protein-protein interaction investigation… (more)

Subjects/Keywords: Chemistry, Physical and theoretical; Protein-protein interactions; Fluorescence; Energy transfer; Biochemistry

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APA (6th Edition):

Xu, F. (2018). Resonance-energy-transfer-based fluorescence imaging and free energy perturbation calculation. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8PP0HKZ

Chicago Manual of Style (16th Edition):

Xu, Fang. “Resonance-energy-transfer-based fluorescence imaging and free energy perturbation calculation.” 2018. Doctoral Dissertation, Columbia University. Accessed June 19, 2019. https://doi.org/10.7916/D8PP0HKZ.

MLA Handbook (7th Edition):

Xu, Fang. “Resonance-energy-transfer-based fluorescence imaging and free energy perturbation calculation.” 2018. Web. 19 Jun 2019.

Vancouver:

Xu F. Resonance-energy-transfer-based fluorescence imaging and free energy perturbation calculation. [Internet] [Doctoral dissertation]. Columbia University; 2018. [cited 2019 Jun 19]. Available from: https://doi.org/10.7916/D8PP0HKZ.

Council of Science Editors:

Xu F. Resonance-energy-transfer-based fluorescence imaging and free energy perturbation calculation. [Doctoral Dissertation]. Columbia University; 2018. Available from: https://doi.org/10.7916/D8PP0HKZ


University of Michigan

12. Ouimet, Claire. Protein Cross-linking Capillary and Microchip Electrophoresis for Protein-Protein Interaction Analysis.

Degree: PhD, Chemistry, 2018, University of Michigan

 Proteins perform their functions as part of multi-protein complexes. These protein complexes are vital for carrying out and regulating cellular processes. As such, there is… (more)

Subjects/Keywords: Capillary Electrophoresis; Protein-Protein Interactions; Microfluidics; Chemistry; Science

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APA (6th Edition):

Ouimet, C. (2018). Protein Cross-linking Capillary and Microchip Electrophoresis for Protein-Protein Interaction Analysis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/147636

Chicago Manual of Style (16th Edition):

Ouimet, Claire. “Protein Cross-linking Capillary and Microchip Electrophoresis for Protein-Protein Interaction Analysis.” 2018. Doctoral Dissertation, University of Michigan. Accessed June 19, 2019. http://hdl.handle.net/2027.42/147636.

MLA Handbook (7th Edition):

Ouimet, Claire. “Protein Cross-linking Capillary and Microchip Electrophoresis for Protein-Protein Interaction Analysis.” 2018. Web. 19 Jun 2019.

Vancouver:

Ouimet C. Protein Cross-linking Capillary and Microchip Electrophoresis for Protein-Protein Interaction Analysis. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/2027.42/147636.

Council of Science Editors:

Ouimet C. Protein Cross-linking Capillary and Microchip Electrophoresis for Protein-Protein Interaction Analysis. [Doctoral Dissertation]. University of Michigan; 2018. Available from: http://hdl.handle.net/2027.42/147636


Utah State University

13. Lundell, Sandra J. Quantum Mechanical Studies of N-H···N Hydrogen Bonding in Acetamide Derivatives and Amino Acids.

Degree: MS, Chemistry and Biochemistry, 2018, Utah State University

  Proteins are made of vast chains of amino acids that twist and fold into intricate designs. These structures are held in place by networks… (more)

Subjects/Keywords: Hydrogen bonding; protein conformation; protein folding; proteins; quantum theory; Chemistry

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APA (6th Edition):

Lundell, S. J. (2018). Quantum Mechanical Studies of N-H···N Hydrogen Bonding in Acetamide Derivatives and Amino Acids. (Masters Thesis). Utah State University. Retrieved from https://digitalcommons.usu.edu/etd/7309

Chicago Manual of Style (16th Edition):

Lundell, Sandra J. “Quantum Mechanical Studies of N-H···N Hydrogen Bonding in Acetamide Derivatives and Amino Acids.” 2018. Masters Thesis, Utah State University. Accessed June 19, 2019. https://digitalcommons.usu.edu/etd/7309.

MLA Handbook (7th Edition):

Lundell, Sandra J. “Quantum Mechanical Studies of N-H···N Hydrogen Bonding in Acetamide Derivatives and Amino Acids.” 2018. Web. 19 Jun 2019.

Vancouver:

Lundell SJ. Quantum Mechanical Studies of N-H···N Hydrogen Bonding in Acetamide Derivatives and Amino Acids. [Internet] [Masters thesis]. Utah State University; 2018. [cited 2019 Jun 19]. Available from: https://digitalcommons.usu.edu/etd/7309.

Council of Science Editors:

Lundell SJ. Quantum Mechanical Studies of N-H···N Hydrogen Bonding in Acetamide Derivatives and Amino Acids. [Masters Thesis]. Utah State University; 2018. Available from: https://digitalcommons.usu.edu/etd/7309

14. Casamayou-Boucau, Yannick. Anisotropy resolved multidimensional emission spectroscopy (ARMES) for the analysis and resolution of insulin oligomer emission.

Degree: 2019, NUI Galway

Protein aggregation is one of the biggest challenges affecting the manufacture and safe use of biopharmaceuticals. Despite efforts made to enhance protein stability [1], aggregation… (more)

Subjects/Keywords: Anisotropy; Fluorescence; Protein; Insulin; Chemometrics; Aggregation; Multidimensional; Spectroscopy; Chemistry; Analytical chemistry

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APA (6th Edition):

Casamayou-Boucau, Y. (2019). Anisotropy resolved multidimensional emission spectroscopy (ARMES) for the analysis and resolution of insulin oligomer emission. (Thesis). NUI Galway. Retrieved from http://hdl.handle.net/10379/14931

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):

Casamayou-Boucau, Yannick. “Anisotropy resolved multidimensional emission spectroscopy (ARMES) for the analysis and resolution of insulin oligomer emission.” 2019. Thesis, NUI Galway. Accessed June 19, 2019. http://hdl.handle.net/10379/14931.

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

MLA Handbook (7th Edition):

Casamayou-Boucau, Yannick. “Anisotropy resolved multidimensional emission spectroscopy (ARMES) for the analysis and resolution of insulin oligomer emission.” 2019. Web. 19 Jun 2019.

Vancouver:

Casamayou-Boucau Y. Anisotropy resolved multidimensional emission spectroscopy (ARMES) for the analysis and resolution of insulin oligomer emission. [Internet] [Thesis]. NUI Galway; 2019. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/10379/14931.

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

Council of Science Editors:

Casamayou-Boucau Y. Anisotropy resolved multidimensional emission spectroscopy (ARMES) for the analysis and resolution of insulin oligomer emission. [Thesis]. NUI Galway; 2019. Available from: http://hdl.handle.net/10379/14931

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


University of Washington

15. Lin, Yu-Ru. Insight from designing ideal αβ monomers and homo-oligomers.

Degree: PhD, 2017, University of Washington

 Previously, general principles relating secondary structure patterns to tertiary packing motifs enable design of different protein topologies stabilized by consistent local and non-local interactions. With… (more)

Subjects/Keywords: De novo protein; Protein Design; Rosetta Design; Biochemistry; Molecular biology; Nanoscience; Biological chemistry

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APA (6th Edition):

Lin, Y. (2017). Insight from designing ideal αβ monomers and homo-oligomers. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/39956

Chicago Manual of Style (16th Edition):

Lin, Yu-Ru. “Insight from designing ideal αβ monomers and homo-oligomers.” 2017. Doctoral Dissertation, University of Washington. Accessed June 19, 2019. http://hdl.handle.net/1773/39956.

MLA Handbook (7th Edition):

Lin, Yu-Ru. “Insight from designing ideal αβ monomers and homo-oligomers.” 2017. Web. 19 Jun 2019.

Vancouver:

Lin Y. Insight from designing ideal αβ monomers and homo-oligomers. [Internet] [Doctoral dissertation]. University of Washington; 2017. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/1773/39956.

Council of Science Editors:

Lin Y. Insight from designing ideal αβ monomers and homo-oligomers. [Doctoral Dissertation]. University of Washington; 2017. Available from: http://hdl.handle.net/1773/39956


University of Washington

16. Frenz, Brandon Michael. Advances In Computer Aided Protein Structure Determination From Sparse Cryo Electron Microscopy Data.

Degree: PhD, 2018, University of Washington

 Single-particle cryo-electron microscopy (cryoEM) has become a powerful tool for determining macromolecular structures. Thanks to recent advances in direct electron detectors and motion correction algorithms… (more)

Subjects/Keywords: Computational Protein Modeling; Cryo electron microscopy; Glycans; Protein Refinement; Rosetta; Biochemistry; Biological chemistry

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

APA (6th Edition):

Frenz, B. M. (2018). Advances In Computer Aided Protein Structure Determination From Sparse Cryo Electron Microscopy Data. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/40847

Chicago Manual of Style (16th Edition):

Frenz, Brandon Michael. “Advances In Computer Aided Protein Structure Determination From Sparse Cryo Electron Microscopy Data.” 2018. Doctoral Dissertation, University of Washington. Accessed June 19, 2019. http://hdl.handle.net/1773/40847.

MLA Handbook (7th Edition):

Frenz, Brandon Michael. “Advances In Computer Aided Protein Structure Determination From Sparse Cryo Electron Microscopy Data.” 2018. Web. 19 Jun 2019.

Vancouver:

Frenz BM. Advances In Computer Aided Protein Structure Determination From Sparse Cryo Electron Microscopy Data. [Internet] [Doctoral dissertation]. University of Washington; 2018. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/1773/40847.

Council of Science Editors:

Frenz BM. Advances In Computer Aided Protein Structure Determination From Sparse Cryo Electron Microscopy Data. [Doctoral Dissertation]. University of Washington; 2018. Available from: http://hdl.handle.net/1773/40847


University of Washington

17. 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 June 19, 2019. 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. 19 Jun 2019.

Vancouver:

Haydon I. De novo protein fusions as platforms for enzyme design. [Internet] [Thesis]. University of Washington; 2019. [cited 2019 Jun 19]. 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


University of California – San Francisco

18. Freilich, Rebecca. Protein-protein interactions of Hsp27.

Degree: Chemistry and Chemical Biology, 2018, University of California – San Francisco

 Small Heat Shock Proteins (sHSPs), including Hsp27, are a non-enzymaticclass of molecular chaperones that bind improperly folded proteins and maintain theirsolubility, acting as a first… (more)

Subjects/Keywords: Biochemistry; Biophysics; Chemistry; Chaperones; Chemical Biology; Hsp27; Protein-Protein Interactions; Small heat shock proteins

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

APA (6th Edition):

Freilich, R. (2018). Protein-protein interactions of Hsp27. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/0g95m86d

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):

Freilich, Rebecca. “Protein-protein interactions of Hsp27.” 2018. Thesis, University of California – San Francisco. Accessed June 19, 2019. http://www.escholarship.org/uc/item/0g95m86d.

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

MLA Handbook (7th Edition):

Freilich, Rebecca. “Protein-protein interactions of Hsp27.” 2018. Web. 19 Jun 2019.

Vancouver:

Freilich R. Protein-protein interactions of Hsp27. [Internet] [Thesis]. University of California – San Francisco; 2018. [cited 2019 Jun 19]. Available from: http://www.escholarship.org/uc/item/0g95m86d.

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

Council of Science Editors:

Freilich R. Protein-protein interactions of Hsp27. [Thesis]. University of California – San Francisco; 2018. Available from: http://www.escholarship.org/uc/item/0g95m86d

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


Arizona State University

19. Petritis, Brianne Ogata. Large-Scale Kinetic Analyses of Protein-Protein Interactions: Advancing the Understanding of Post Translational Modifications in Biological Regulation.

Degree: Biological Design, 2018, Arizona State University

 Signal transduction networks comprising protein-protein interactions (PPIs) mediate homeostatic, diseased, and therapeutic cellular responses. Mapping these networks has primarily focused on identifying interactors, but less… (more)

Subjects/Keywords: Biochemistry; Molecular biology; Physical chemistry; kinetics; NAPPA; protein microarray; protein-protein interactions; SPRi; surface plasmon resonance

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APA (6th Edition):

Petritis, B. O. (2018). Large-Scale Kinetic Analyses of Protein-Protein Interactions: Advancing the Understanding of Post Translational Modifications in Biological Regulation. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/49378

Chicago Manual of Style (16th Edition):

Petritis, Brianne Ogata. “Large-Scale Kinetic Analyses of Protein-Protein Interactions: Advancing the Understanding of Post Translational Modifications in Biological Regulation.” 2018. Doctoral Dissertation, Arizona State University. Accessed June 19, 2019. http://repository.asu.edu/items/49378.

MLA Handbook (7th Edition):

Petritis, Brianne Ogata. “Large-Scale Kinetic Analyses of Protein-Protein Interactions: Advancing the Understanding of Post Translational Modifications in Biological Regulation.” 2018. Web. 19 Jun 2019.

Vancouver:

Petritis BO. Large-Scale Kinetic Analyses of Protein-Protein Interactions: Advancing the Understanding of Post Translational Modifications in Biological Regulation. [Internet] [Doctoral dissertation]. Arizona State University; 2018. [cited 2019 Jun 19]. Available from: http://repository.asu.edu/items/49378.

Council of Science Editors:

Petritis BO. Large-Scale Kinetic Analyses of Protein-Protein Interactions: Advancing the Understanding of Post Translational Modifications in Biological Regulation. [Doctoral Dissertation]. Arizona State University; 2018. Available from: http://repository.asu.edu/items/49378


University of California – Irvine

20. Schaub, Andrew Joseph. Development and Application of a Computational Force Field for the Study of Structure, Function and Motion of Enzymes in the Acetate and Non-ribosomal Peptide Pathways.

Degree: Chemistry, 2018, University of California – Irvine

 Enzymes in the acetate and non-ribosomal peptide pathways generate chemically diverse and complex bioactive molecules, with the intermediates being chauffeured between catalytic partners via a… (more)

Subjects/Keywords: Computational chemistry; Physical chemistry; Biochemistry; force field; molecular dynamics; natural products; polyketide; protein engineering; protein interactions

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APA (6th Edition):

Schaub, A. J. (2018). Development and Application of a Computational Force Field for the Study of Structure, Function and Motion of Enzymes in the Acetate and Non-ribosomal Peptide Pathways. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/1nk6x5t5

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):

Schaub, Andrew Joseph. “Development and Application of a Computational Force Field for the Study of Structure, Function and Motion of Enzymes in the Acetate and Non-ribosomal Peptide Pathways.” 2018. Thesis, University of California – Irvine. Accessed June 19, 2019. http://www.escholarship.org/uc/item/1nk6x5t5.

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

MLA Handbook (7th Edition):

Schaub, Andrew Joseph. “Development and Application of a Computational Force Field for the Study of Structure, Function and Motion of Enzymes in the Acetate and Non-ribosomal Peptide Pathways.” 2018. Web. 19 Jun 2019.

Vancouver:

Schaub AJ. Development and Application of a Computational Force Field for the Study of Structure, Function and Motion of Enzymes in the Acetate and Non-ribosomal Peptide Pathways. [Internet] [Thesis]. University of California – Irvine; 2018. [cited 2019 Jun 19]. Available from: http://www.escholarship.org/uc/item/1nk6x5t5.

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

Council of Science Editors:

Schaub AJ. Development and Application of a Computational Force Field for the Study of Structure, Function and Motion of Enzymes in the Acetate and Non-ribosomal Peptide Pathways. [Thesis]. University of California – Irvine; 2018. Available from: http://www.escholarship.org/uc/item/1nk6x5t5

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


Western Kentucky University

21. Ha, Dat Thinh. Developing a New Sensing Technology for Double-Stranded DNA Detection Utilizing Engineered Zinc Finger Proteins and Nanomaterials.

Degree: MS, Department of Chemistry, 2018, Western Kentucky University

  A specific double-stranded DNA sensing system is of great interest for diagnostic and other biomedical applications. Zinc finger domains, which recognize double-stranded DNA, can… (more)

Subjects/Keywords: DNA diagnostic; Protein engineering; Protein assay; Graphene Oxide-based detection; Analytical Chemistry; Biochemistry, Biophysics, and Structural Biology; Chemistry

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

APA (6th Edition):

Ha, D. T. (2018). Developing a New Sensing Technology for Double-Stranded DNA Detection Utilizing Engineered Zinc Finger Proteins and Nanomaterials. (Masters Thesis). Western Kentucky University. Retrieved from https://digitalcommons.wku.edu/theses/3079

Chicago Manual of Style (16th Edition):

Ha, Dat Thinh. “Developing a New Sensing Technology for Double-Stranded DNA Detection Utilizing Engineered Zinc Finger Proteins and Nanomaterials.” 2018. Masters Thesis, Western Kentucky University. Accessed June 19, 2019. https://digitalcommons.wku.edu/theses/3079.

MLA Handbook (7th Edition):

Ha, Dat Thinh. “Developing a New Sensing Technology for Double-Stranded DNA Detection Utilizing Engineered Zinc Finger Proteins and Nanomaterials.” 2018. Web. 19 Jun 2019.

Vancouver:

Ha DT. Developing a New Sensing Technology for Double-Stranded DNA Detection Utilizing Engineered Zinc Finger Proteins and Nanomaterials. [Internet] [Masters thesis]. Western Kentucky University; 2018. [cited 2019 Jun 19]. Available from: https://digitalcommons.wku.edu/theses/3079.

Council of Science Editors:

Ha DT. Developing a New Sensing Technology for Double-Stranded DNA Detection Utilizing Engineered Zinc Finger Proteins and Nanomaterials. [Masters Thesis]. Western Kentucky University; 2018. Available from: https://digitalcommons.wku.edu/theses/3079

22. Freese, Allison Kimberly. Synthesis, Stabilization, and Modification of Zinc Oxide Nanoparticles for Biological Applications.

Degree: MSin Chemistry, Chemistry, 2019, Missouri State University

  Nanoparticles have become very useful as delivery systems in biomedicine. The nanoparticles can be layered with different compounds to produce a vessel for transport… (more)

Subjects/Keywords: zinc oxide; protein; protein delivery; lysozyme; RNA; nanoparticles; nanomaterials; layer-by-layer; Analytical Chemistry; Biochemistry; Inorganic Chemistry

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

APA (6th Edition):

Freese, A. K. (2019). Synthesis, Stabilization, and Modification of Zinc Oxide Nanoparticles for Biological Applications. (Masters Thesis). Missouri State University. Retrieved from https://bearworks.missouristate.edu/theses/3370

Chicago Manual of Style (16th Edition):

Freese, Allison Kimberly. “Synthesis, Stabilization, and Modification of Zinc Oxide Nanoparticles for Biological Applications.” 2019. Masters Thesis, Missouri State University. Accessed June 19, 2019. https://bearworks.missouristate.edu/theses/3370.

MLA Handbook (7th Edition):

Freese, Allison Kimberly. “Synthesis, Stabilization, and Modification of Zinc Oxide Nanoparticles for Biological Applications.” 2019. Web. 19 Jun 2019.

Vancouver:

Freese AK. Synthesis, Stabilization, and Modification of Zinc Oxide Nanoparticles for Biological Applications. [Internet] [Masters thesis]. Missouri State University; 2019. [cited 2019 Jun 19]. Available from: https://bearworks.missouristate.edu/theses/3370.

Council of Science Editors:

Freese AK. Synthesis, Stabilization, and Modification of Zinc Oxide Nanoparticles for Biological Applications. [Masters Thesis]. Missouri State University; 2019. Available from: https://bearworks.missouristate.edu/theses/3370


University of Western Ontario

23. Xiao, Yiming. Hydrogen-Deuterium Exchange Mass Spectrometry and Molecular Dynamics Simulations for Studying Protein Structure and Dynamics.

Degree: 2018, University of Western Ontario

 Deciphering properties of proteins are essential for human health and aiding in the development of new pharmaceuticals. This dissertation uses hydrogen-deuterium exchange (HDX) mass spectrometry… (more)

Subjects/Keywords: protein dynamics; hydrogen-deuterium exchange; mass spectrometry; molecular dynamics simulation; S100A11; Analytical Chemistry; Physical Chemistry

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APA (6th Edition):

Xiao, Y. (2018). Hydrogen-Deuterium Exchange Mass Spectrometry and Molecular Dynamics Simulations for Studying Protein Structure and Dynamics. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/5713

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):

Xiao, Yiming. “Hydrogen-Deuterium Exchange Mass Spectrometry and Molecular Dynamics Simulations for Studying Protein Structure and Dynamics.” 2018. Thesis, University of Western Ontario. Accessed June 19, 2019. https://ir.lib.uwo.ca/etd/5713.

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

MLA Handbook (7th Edition):

Xiao, Yiming. “Hydrogen-Deuterium Exchange Mass Spectrometry and Molecular Dynamics Simulations for Studying Protein Structure and Dynamics.” 2018. Web. 19 Jun 2019.

Vancouver:

Xiao Y. Hydrogen-Deuterium Exchange Mass Spectrometry and Molecular Dynamics Simulations for Studying Protein Structure and Dynamics. [Internet] [Thesis]. University of Western Ontario; 2018. [cited 2019 Jun 19]. Available from: https://ir.lib.uwo.ca/etd/5713.

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

Council of Science Editors:

Xiao Y. Hydrogen-Deuterium Exchange Mass Spectrometry and Molecular Dynamics Simulations for Studying Protein Structure and Dynamics. [Thesis]. University of Western Ontario; 2018. Available from: https://ir.lib.uwo.ca/etd/5713

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


University of Washington

24. Edwards, Thomas Howard. New Statistical Inference Methods for DEER Spectroscopy on Proteins.

Degree: PhD, 2018, University of Washington

 Double Electron-Electron Resonance (DEER) spectroscopy is a pulse-EPR experiment that can provide sub-ångström resolution distance measurements of proteins and other biomacro- molecules in the distance… (more)

Subjects/Keywords: Bayesian Statistics; DEER; EPR; MCMC; Protein; Tikhonov Regularization; Biophysics; Physical chemistry; Chemistry

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APA (6th Edition):

Edwards, T. H. (2018). New Statistical Inference Methods for DEER Spectroscopy on Proteins. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/43000

Chicago Manual of Style (16th Edition):

Edwards, Thomas Howard. “New Statistical Inference Methods for DEER Spectroscopy on Proteins.” 2018. Doctoral Dissertation, University of Washington. Accessed June 19, 2019. http://hdl.handle.net/1773/43000.

MLA Handbook (7th Edition):

Edwards, Thomas Howard. “New Statistical Inference Methods for DEER Spectroscopy on Proteins.” 2018. Web. 19 Jun 2019.

Vancouver:

Edwards TH. New Statistical Inference Methods for DEER Spectroscopy on Proteins. [Internet] [Doctoral dissertation]. University of Washington; 2018. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/1773/43000.

Council of Science Editors:

Edwards TH. New Statistical Inference Methods for DEER Spectroscopy on Proteins. [Doctoral Dissertation]. University of Washington; 2018. Available from: http://hdl.handle.net/1773/43000


University of Washington

25. Ueda, George Thomas. Computational Design of Symmetric Protein Complexes with Implications for Vaccine and Biotherapeutic Development.

Degree: PhD, 2019, University of Washington

 Using a newly developed computational docking and scoring method combined with Rosetta two-sided interface design, we demonstrated accurate design of self-assembling oligomeric proteins that exhibit… (more)

Subjects/Keywords: Biotherapeutic; Computational; Design; Engineering; Protein; Vaccine; Biochemistry; Bioengineering; Computational chemistry; Biological chemistry

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

APA (6th Edition):

Ueda, G. T. (2019). Computational Design of Symmetric Protein Complexes with Implications for Vaccine and Biotherapeutic Development. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/43303

Chicago Manual of Style (16th Edition):

Ueda, George Thomas. “Computational Design of Symmetric Protein Complexes with Implications for Vaccine and Biotherapeutic Development.” 2019. Doctoral Dissertation, University of Washington. Accessed June 19, 2019. http://hdl.handle.net/1773/43303.

MLA Handbook (7th Edition):

Ueda, George Thomas. “Computational Design of Symmetric Protein Complexes with Implications for Vaccine and Biotherapeutic Development.” 2019. Web. 19 Jun 2019.

Vancouver:

Ueda GT. Computational Design of Symmetric Protein Complexes with Implications for Vaccine and Biotherapeutic Development. [Internet] [Doctoral dissertation]. University of Washington; 2019. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/1773/43303.

Council of Science Editors:

Ueda GT. Computational Design of Symmetric Protein Complexes with Implications for Vaccine and Biotherapeutic Development. [Doctoral Dissertation]. University of Washington; 2019. Available from: http://hdl.handle.net/1773/43303


The Ohio State University

26. Yu, Lei. Molecular Dynamics of Folded and Disordered Polypeptides in Comparison with Nuclear Magnetic Resonance Measurement.

Degree: MS, Chemistry, 2018, The Ohio State University

 With continuous increase in computer speed, molecular dynamics (MD) simulations have become a crucial biophysical method for the understanding of biochemical processes at atomic detail.… (more)

Subjects/Keywords: Biophysics; Chemistry; Physical Chemistry; Molecular Dynamics; Nuclear Magnetic Resonance; Intrinsically Disordered Protein

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APA (6th Edition):

Yu, L. (2018). Molecular Dynamics of Folded and Disordered Polypeptides in Comparison with Nuclear Magnetic Resonance Measurement. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1521650422218055

Chicago Manual of Style (16th Edition):

Yu, Lei. “Molecular Dynamics of Folded and Disordered Polypeptides in Comparison with Nuclear Magnetic Resonance Measurement.” 2018. Masters Thesis, The Ohio State University. Accessed June 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1521650422218055.

MLA Handbook (7th Edition):

Yu, Lei. “Molecular Dynamics of Folded and Disordered Polypeptides in Comparison with Nuclear Magnetic Resonance Measurement.” 2018. Web. 19 Jun 2019.

Vancouver:

Yu L. Molecular Dynamics of Folded and Disordered Polypeptides in Comparison with Nuclear Magnetic Resonance Measurement. [Internet] [Masters thesis]. The Ohio State University; 2018. [cited 2019 Jun 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1521650422218055.

Council of Science Editors:

Yu L. Molecular Dynamics of Folded and Disordered Polypeptides in Comparison with Nuclear Magnetic Resonance Measurement. [Masters Thesis]. The Ohio State University; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1521650422218055


Bucknell University

27. Hartnett, Sean. Stability of Bimetallic Clusters in Protein Model Systems.

Degree: 2018, Bucknell University

 Heterobimetallic cofactors are commonly found in proteins and allow them to perform unique chemical processes that would otherwise not be possible. The interactions between these… (more)

Subjects/Keywords: metalloclusters; heterobimetallic; protein model systems; thermodynamic exchange; HXTA; Analytical Chemistry; Inorganic Chemistry

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APA (6th Edition):

Hartnett, S. (2018). Stability of Bimetallic Clusters in Protein Model Systems. (Thesis). Bucknell University. Retrieved from https://digitalcommons.bucknell.edu/masters_theses/214

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):

Hartnett, Sean. “Stability of Bimetallic Clusters in Protein Model Systems.” 2018. Thesis, Bucknell University. Accessed June 19, 2019. https://digitalcommons.bucknell.edu/masters_theses/214.

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

MLA Handbook (7th Edition):

Hartnett, Sean. “Stability of Bimetallic Clusters in Protein Model Systems.” 2018. Web. 19 Jun 2019.

Vancouver:

Hartnett S. Stability of Bimetallic Clusters in Protein Model Systems. [Internet] [Thesis]. Bucknell University; 2018. [cited 2019 Jun 19]. Available from: https://digitalcommons.bucknell.edu/masters_theses/214.

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

Council of Science Editors:

Hartnett S. Stability of Bimetallic Clusters in Protein Model Systems. [Thesis]. Bucknell University; 2018. Available from: https://digitalcommons.bucknell.edu/masters_theses/214

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


University of California – San Diego

28. Monferrer i Sureda, Alba. Versatile Kit of Nanoshapes Self-Assembling from RNA and DNA Modules.

Degree: Chemistry, 2018, University of California – San Diego

 DNA and RNA have emerged as a material for nanotechnology applications that capitalize on the nucleic acids’ ability to encode folding and programmable self-assembly through… (more)

Subjects/Keywords: Chemistry; Nanotechnology; DNA; hybrid; nanotechnology; protein binding; RNA

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APA (6th Edition):

Monferrer i Sureda, A. (2018). Versatile Kit of Nanoshapes Self-Assembling from RNA and DNA Modules. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/8g0954kn

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):

Monferrer i Sureda, Alba. “Versatile Kit of Nanoshapes Self-Assembling from RNA and DNA Modules.” 2018. Thesis, University of California – San Diego. Accessed June 19, 2019. http://www.escholarship.org/uc/item/8g0954kn.

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

MLA Handbook (7th Edition):

Monferrer i Sureda, Alba. “Versatile Kit of Nanoshapes Self-Assembling from RNA and DNA Modules.” 2018. Web. 19 Jun 2019.

Vancouver:

Monferrer i Sureda A. Versatile Kit of Nanoshapes Self-Assembling from RNA and DNA Modules. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2019 Jun 19]. Available from: http://www.escholarship.org/uc/item/8g0954kn.

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

Council of Science Editors:

Monferrer i Sureda A. Versatile Kit of Nanoshapes Self-Assembling from RNA and DNA Modules. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/8g0954kn

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


University of Oklahoma

29. Nunez, Juan. THE LIGAND BINDING PROPERTIES OF THE OXYSTEROL-BINDING PROTEIN FAMILY SUBFAMILY-I.

Degree: PhD, 2018, University of Oklahoma

 The oxysterol-binding protein/OSBP-related proteins (OSBP/ORPs) are a family of proteins conserved in all eukaryotes that have complex biological activities connected to lipid transport and lipid… (more)

Subjects/Keywords: Chemistry, Biochemistry.; Oxysterols; Oxysterol Binding Protein; OSW-1

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APA (6th Edition):

Nunez, J. (2018). THE LIGAND BINDING PROPERTIES OF THE OXYSTEROL-BINDING PROTEIN FAMILY SUBFAMILY-I. (Doctoral Dissertation). University of Oklahoma. Retrieved from http://hdl.handle.net/11244/316795

Chicago Manual of Style (16th Edition):

Nunez, Juan. “THE LIGAND BINDING PROPERTIES OF THE OXYSTEROL-BINDING PROTEIN FAMILY SUBFAMILY-I.” 2018. Doctoral Dissertation, University of Oklahoma. Accessed June 19, 2019. http://hdl.handle.net/11244/316795.

MLA Handbook (7th Edition):

Nunez, Juan. “THE LIGAND BINDING PROPERTIES OF THE OXYSTEROL-BINDING PROTEIN FAMILY SUBFAMILY-I.” 2018. Web. 19 Jun 2019.

Vancouver:

Nunez J. THE LIGAND BINDING PROPERTIES OF THE OXYSTEROL-BINDING PROTEIN FAMILY SUBFAMILY-I. [Internet] [Doctoral dissertation]. University of Oklahoma; 2018. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/11244/316795.

Council of Science Editors:

Nunez J. THE LIGAND BINDING PROPERTIES OF THE OXYSTEROL-BINDING PROTEIN FAMILY SUBFAMILY-I. [Doctoral Dissertation]. University of Oklahoma; 2018. Available from: http://hdl.handle.net/11244/316795


UCLA

30. Hatfield, Daniel John. De Nove Design of a Palladium-Containing Metallo-Enzyme.

Degree: Chemistry, 2018, UCLA

Protein design is a challenging endeavor that attempts to harness the power of nature and engineer it to a particular task. The use of a… (more)

Subjects/Keywords: Computational chemistry; Enzyme; Palladium; Protein Design; QM/DMD; Simulation

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

APA (6th Edition):

Hatfield, D. J. (2018). De Nove Design of a Palladium-Containing Metallo-Enzyme. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/9p26m7z2

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):

Hatfield, Daniel John. “De Nove Design of a Palladium-Containing Metallo-Enzyme.” 2018. Thesis, UCLA. Accessed June 19, 2019. http://www.escholarship.org/uc/item/9p26m7z2.

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

MLA Handbook (7th Edition):

Hatfield, Daniel John. “De Nove Design of a Palladium-Containing Metallo-Enzyme.” 2018. Web. 19 Jun 2019.

Vancouver:

Hatfield DJ. De Nove Design of a Palladium-Containing Metallo-Enzyme. [Internet] [Thesis]. UCLA; 2018. [cited 2019 Jun 19]. Available from: http://www.escholarship.org/uc/item/9p26m7z2.

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

Council of Science Editors:

Hatfield DJ. De Nove Design of a Palladium-Containing Metallo-Enzyme. [Thesis]. UCLA; 2018. Available from: http://www.escholarship.org/uc/item/9p26m7z2

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

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