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Dates: 2010 – 2014

You searched for subject:(Protein chemistry). Showing records 1 – 30 of 523 total matches.

[1] [2] [3] [4] [5] … [18]

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1. Richter, Anja. Synthese niedermolekularer Verbindungen zur Stabilisierung von Protein-Protein-Interaktionen.

Degree: 2011, Technische Universität Dortmund

 Die phytotoxische Wirkung des Naturstoffs Fusiocccin A, erstmals isoliert von Ballio et al. aus dem Pilz Fusicoccum amygadali, lässt sich auf die Stabilisierung der Interaktion… (more)

Subjects/Keywords: Fusicoccin; Organische Chemie; Protein-Protein-Interaktionen; Totalsynthese; 540; 570

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APA (6th Edition):

Richter, A. (2011). Synthese niedermolekularer Verbindungen zur Stabilisierung von Protein-Protein-Interaktionen. (Thesis). Technische Universität Dortmund. Retrieved from http://hdl.handle.net/2003/29051

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):

Richter, Anja. “Synthese niedermolekularer Verbindungen zur Stabilisierung von Protein-Protein-Interaktionen.” 2011. Thesis, Technische Universität Dortmund. Accessed June 19, 2019. http://hdl.handle.net/2003/29051.

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

MLA Handbook (7th Edition):

Richter, Anja. “Synthese niedermolekularer Verbindungen zur Stabilisierung von Protein-Protein-Interaktionen.” 2011. Web. 19 Jun 2019.

Vancouver:

Richter A. Synthese niedermolekularer Verbindungen zur Stabilisierung von Protein-Protein-Interaktionen. [Internet] [Thesis]. Technische Universität Dortmund; 2011. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/2003/29051.

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

Council of Science Editors:

Richter A. Synthese niedermolekularer Verbindungen zur Stabilisierung von Protein-Protein-Interaktionen. [Thesis]. Technische Universität Dortmund; 2011. Available from: http://hdl.handle.net/2003/29051

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


University of New Mexico

2. Bryan, Tyrel. Criteria for Evolution of Successful Proteins: Fold Fitness and Domain Dynamics Explored.

Degree: Department of Chemistry and Chemical Biology, 2014, University of New Mexico

  The Haloacid Dehalogenase Superfamily (HADSF) is a ubiquitous family of enzyme with more than 32,000 members. A variety of reactions are catalyzed by HAD… (more)

Subjects/Keywords: Protein Folding; Chemistry; Physical Chemistry

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APA (6th Edition):

Bryan, T. (2014). Criteria for Evolution of Successful Proteins: Fold Fitness and Domain Dynamics Explored. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/chem_etds/35

Chicago Manual of Style (16th Edition):

Bryan, Tyrel. “Criteria for Evolution of Successful Proteins: Fold Fitness and Domain Dynamics Explored.” 2014. Doctoral Dissertation, University of New Mexico. Accessed June 19, 2019. https://digitalrepository.unm.edu/chem_etds/35.

MLA Handbook (7th Edition):

Bryan, Tyrel. “Criteria for Evolution of Successful Proteins: Fold Fitness and Domain Dynamics Explored.” 2014. Web. 19 Jun 2019.

Vancouver:

Bryan T. Criteria for Evolution of Successful Proteins: Fold Fitness and Domain Dynamics Explored. [Internet] [Doctoral dissertation]. University of New Mexico; 2014. [cited 2019 Jun 19]. Available from: https://digitalrepository.unm.edu/chem_etds/35.

Council of Science Editors:

Bryan T. Criteria for Evolution of Successful Proteins: Fold Fitness and Domain Dynamics Explored. [Doctoral Dissertation]. University of New Mexico; 2014. Available from: https://digitalrepository.unm.edu/chem_etds/35


University of Rochester

3. Park, Min Sun. Computational Studies of Proteins: Dynamics and Interactions with Small Molecules.

Degree: PhD, 2011, University of Rochester

 Understanding protein dynamics is important for drug design. G proteins play an important role in cellular signal transduction and are involved in many processes. They… (more)

Subjects/Keywords: Computational Chemistry; Virtual Screening; Protein-Protein Interaction

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APA (6th Edition):

Park, M. S. (2011). Computational Studies of Proteins: Dynamics and Interactions with Small Molecules. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/15859

Chicago Manual of Style (16th Edition):

Park, Min Sun. “Computational Studies of Proteins: Dynamics and Interactions with Small Molecules.” 2011. Doctoral Dissertation, University of Rochester. Accessed June 19, 2019. http://hdl.handle.net/1802/15859.

MLA Handbook (7th Edition):

Park, Min Sun. “Computational Studies of Proteins: Dynamics and Interactions with Small Molecules.” 2011. Web. 19 Jun 2019.

Vancouver:

Park MS. Computational Studies of Proteins: Dynamics and Interactions with Small Molecules. [Internet] [Doctoral dissertation]. University of Rochester; 2011. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/1802/15859.

Council of Science Editors:

Park MS. Computational Studies of Proteins: Dynamics and Interactions with Small Molecules. [Doctoral Dissertation]. University of Rochester; 2011. Available from: http://hdl.handle.net/1802/15859


The Ohio State University

4. Luechapanichkul, Rinrada. Determination of the Sequence Specificity and Protein Substrates of Protein Phosphatases.

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

Protein phosphorylation is a post-translational modification controlled by two counteracting enzyme families, protein kinases and phosphatases. Protein phosphatases have been demonstrated to regulate many… (more)

Subjects/Keywords: Chemistry; protein phosphatases, sequence specificity

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APA (6th Edition):

Luechapanichkul, R. (2014). Determination of the Sequence Specificity and Protein Substrates of Protein Phosphatases. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1398868380

Chicago Manual of Style (16th Edition):

Luechapanichkul, Rinrada. “Determination of the Sequence Specificity and Protein Substrates of Protein Phosphatases.” 2014. Doctoral Dissertation, The Ohio State University. Accessed June 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1398868380.

MLA Handbook (7th Edition):

Luechapanichkul, Rinrada. “Determination of the Sequence Specificity and Protein Substrates of Protein Phosphatases.” 2014. Web. 19 Jun 2019.

Vancouver:

Luechapanichkul R. Determination of the Sequence Specificity and Protein Substrates of Protein Phosphatases. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2019 Jun 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1398868380.

Council of Science Editors:

Luechapanichkul R. Determination of the Sequence Specificity and Protein Substrates of Protein Phosphatases. [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1398868380


National University of Ireland – Galway

5. McGovern, Róise Ella. Calixarene-mediated protein assembly .

Degree: 2014, National University of Ireland – Galway

 Solved the first crystal structure of a protein-calixarene complex (at 1.4 Angstrom resolution). The results provide exact structural information on the amino acid preference of… (more)

Subjects/Keywords: Protein assembly; Calixarene; Chemistry

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APA (6th Edition):

McGovern, R. E. (2014). Calixarene-mediated protein assembly . (Thesis). National University of Ireland – Galway. Retrieved from http://hdl.handle.net/10379/4552

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):

McGovern, Róise Ella. “Calixarene-mediated protein assembly .” 2014. Thesis, National University of Ireland – Galway. Accessed June 19, 2019. http://hdl.handle.net/10379/4552.

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

MLA Handbook (7th Edition):

McGovern, Róise Ella. “Calixarene-mediated protein assembly .” 2014. Web. 19 Jun 2019.

Vancouver:

McGovern RE. Calixarene-mediated protein assembly . [Internet] [Thesis]. National University of Ireland – Galway; 2014. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/10379/4552.

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

Council of Science Editors:

McGovern RE. Calixarene-mediated protein assembly . [Thesis]. National University of Ireland – Galway; 2014. Available from: http://hdl.handle.net/10379/4552

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


University of Vienna

6. Weber, Christine. Investigations into the interaction between the beta-secretase protein BACE1 and a member of the reticulon family, RTN3.

Degree: 2010, University of Vienna

Mit steigender Prävalenz von Morbus Alzheimer in den Industrienationen wird auch die bisher erfolglose Suche nach einer effektiven Pharmakotherapie immer dringlicher. Gegenwärtig verfügbare Medikamente verbessern… (more)

Subjects/Keywords: 44.42 Pharmazeutische Chemie; Alzheimer / beta-Secretase Inhibitoren / Protein Interaktionen; Alzheimer's disease / beta-secretase inhibitors / protein-protein interactions

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APA (6th Edition):

Weber, C. (2010). Investigations into the interaction between the beta-secretase protein BACE1 and a member of the reticulon family, RTN3. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/8628/

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):

Weber, Christine. “Investigations into the interaction between the beta-secretase protein BACE1 and a member of the reticulon family, RTN3.” 2010. Thesis, University of Vienna. Accessed June 19, 2019. http://othes.univie.ac.at/8628/.

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

MLA Handbook (7th Edition):

Weber, Christine. “Investigations into the interaction between the beta-secretase protein BACE1 and a member of the reticulon family, RTN3.” 2010. Web. 19 Jun 2019.

Vancouver:

Weber C. Investigations into the interaction between the beta-secretase protein BACE1 and a member of the reticulon family, RTN3. [Internet] [Thesis]. University of Vienna; 2010. [cited 2019 Jun 19]. Available from: http://othes.univie.ac.at/8628/.

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

Council of Science Editors:

Weber C. Investigations into the interaction between the beta-secretase protein BACE1 and a member of the reticulon family, RTN3. [Thesis]. University of Vienna; 2010. Available from: http://othes.univie.ac.at/8628/

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


University of Oxford

7. Gunnoo, Smita Bye. Site-specific chemical modification of antibodies for the modulation of function.

Degree: PhD, 2013, University of Oxford

 Chemical modification of antibodies is critical for many research areas including therapeutic and biotechnological applications. In particular, strategies for site-specific chemical modification via non-natural amino… (more)

Subjects/Keywords: 547; Organic chemistry; Chemical Biology; Protein chemistry

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APA (6th Edition):

Gunnoo, S. B. (2013). Site-specific chemical modification of antibodies for the modulation of function. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:8857b207-c70d-4656-8279-9bcbfce2a8bd ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644879

Chicago Manual of Style (16th Edition):

Gunnoo, Smita Bye. “Site-specific chemical modification of antibodies for the modulation of function.” 2013. Doctoral Dissertation, University of Oxford. Accessed June 19, 2019. http://ora.ox.ac.uk/objects/uuid:8857b207-c70d-4656-8279-9bcbfce2a8bd ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644879.

MLA Handbook (7th Edition):

Gunnoo, Smita Bye. “Site-specific chemical modification of antibodies for the modulation of function.” 2013. Web. 19 Jun 2019.

Vancouver:

Gunnoo SB. Site-specific chemical modification of antibodies for the modulation of function. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2019 Jun 19]. Available from: http://ora.ox.ac.uk/objects/uuid:8857b207-c70d-4656-8279-9bcbfce2a8bd ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644879.

Council of Science Editors:

Gunnoo SB. Site-specific chemical modification of antibodies for the modulation of function. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:8857b207-c70d-4656-8279-9bcbfce2a8bd ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644879

8. Flanagan, Sean E. Hetero-Protein Coacervation and Complex Equilibria Between β-lactoglobulin and Lactoferrin.

Degree: MS(M.S.), Chemistry, 2014, U of Massachusetts : Masters

  Coacervation between the milk proteins β-lactoglobulin (BLG) and Lactoferrin (LF) was studied as a model system for hetero-protein coacervation (HPC). Equilibria among BLG/LF complexes… (more)

Subjects/Keywords: Coacervation; Hetero-Protein Coacervation; Protein-Protein Interactions; Complex Equilibrium; Lactoferrin; β-lactoglobulin; Analytical Chemistry; Biochemistry; Food Chemistry; Physical Chemistry; Polymer Chemistry

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APA (6th Edition):

Flanagan, S. E. (2014). Hetero-Protein Coacervation and Complex Equilibria Between β-lactoglobulin and Lactoferrin. (Masters Thesis). U of Massachusetts : Masters. Retrieved from http://scholarworks.umass.edu/theses/1179

Chicago Manual of Style (16th Edition):

Flanagan, Sean E. “Hetero-Protein Coacervation and Complex Equilibria Between β-lactoglobulin and Lactoferrin.” 2014. Masters Thesis, U of Massachusetts : Masters. Accessed June 19, 2019. http://scholarworks.umass.edu/theses/1179.

MLA Handbook (7th Edition):

Flanagan, Sean E. “Hetero-Protein Coacervation and Complex Equilibria Between β-lactoglobulin and Lactoferrin.” 2014. Web. 19 Jun 2019.

Vancouver:

Flanagan SE. Hetero-Protein Coacervation and Complex Equilibria Between β-lactoglobulin and Lactoferrin. [Internet] [Masters thesis]. U of Massachusetts : Masters; 2014. [cited 2019 Jun 19]. Available from: http://scholarworks.umass.edu/theses/1179.

Council of Science Editors:

Flanagan SE. Hetero-Protein Coacervation and Complex Equilibria Between β-lactoglobulin and Lactoferrin. [Masters Thesis]. U of Massachusetts : Masters; 2014. Available from: http://scholarworks.umass.edu/theses/1179


University of South Florida

9. Du Boulay, Courtney Jerome. Virtual Screening for Inhibitors of Anti-apoptotic Proteins: DCK, BCL-XL, MCL-1, MDMX, and MDM2.

Degree: 2013, University of South Florida

 ←Within this dissertation the topic of virtual screening is discussed with regard to three different cancer targets and also a brief introduction of the tools… (more)

Subjects/Keywords: Cancer; Computational Chemistry; Medicinal Chemistry; Medicine; Protein Protein Interaction; Virtual Screening; Chemistry

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APA (6th Edition):

Du Boulay, C. J. (2013). Virtual Screening for Inhibitors of Anti-apoptotic Proteins: DCK, BCL-XL, MCL-1, MDMX, and MDM2. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/4664

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):

Du Boulay, Courtney Jerome. “Virtual Screening for Inhibitors of Anti-apoptotic Proteins: DCK, BCL-XL, MCL-1, MDMX, and MDM2.” 2013. Thesis, University of South Florida. Accessed June 19, 2019. https://scholarcommons.usf.edu/etd/4664.

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

MLA Handbook (7th Edition):

Du Boulay, Courtney Jerome. “Virtual Screening for Inhibitors of Anti-apoptotic Proteins: DCK, BCL-XL, MCL-1, MDMX, and MDM2.” 2013. Web. 19 Jun 2019.

Vancouver:

Du Boulay CJ. Virtual Screening for Inhibitors of Anti-apoptotic Proteins: DCK, BCL-XL, MCL-1, MDMX, and MDM2. [Internet] [Thesis]. University of South Florida; 2013. [cited 2019 Jun 19]. Available from: https://scholarcommons.usf.edu/etd/4664.

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

Council of Science Editors:

Du Boulay CJ. Virtual Screening for Inhibitors of Anti-apoptotic Proteins: DCK, BCL-XL, MCL-1, MDMX, and MDM2. [Thesis]. University of South Florida; 2013. Available from: https://scholarcommons.usf.edu/etd/4664

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


University of Michigan

10. Abulwerdi, Fardokht Assadi. Structure-Based Design, Synthesis and Evaluation of Novel and Selective Small-Molecule Inhibitors of the Anti-Apoptotic Protein Mcl-1.

Degree: PhD, Medicinal Chemistry, 2014, University of Michigan

 The mitochondrial pathway to apoptosis is regulated through the protein-protein interactions of pro- and anti-apoptotic members of Bcl-2 family proteins. Overexpression of the anti-apoptotic members… (more)

Subjects/Keywords: Anti-apoptotic Mcl-1; Medicinal Chemistry; Protein-protein Interaction Inhibitor; Cancer; Protein NMR Spectroscopy; Structure-activity Relationship; Biological Chemistry; Chemistry; Science

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APA (6th Edition):

Abulwerdi, F. A. (2014). Structure-Based Design, Synthesis and Evaluation of Novel and Selective Small-Molecule Inhibitors of the Anti-Apoptotic Protein Mcl-1. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/107109

Chicago Manual of Style (16th Edition):

Abulwerdi, Fardokht Assadi. “Structure-Based Design, Synthesis and Evaluation of Novel and Selective Small-Molecule Inhibitors of the Anti-Apoptotic Protein Mcl-1.” 2014. Doctoral Dissertation, University of Michigan. Accessed June 19, 2019. http://hdl.handle.net/2027.42/107109.

MLA Handbook (7th Edition):

Abulwerdi, Fardokht Assadi. “Structure-Based Design, Synthesis and Evaluation of Novel and Selective Small-Molecule Inhibitors of the Anti-Apoptotic Protein Mcl-1.” 2014. Web. 19 Jun 2019.

Vancouver:

Abulwerdi FA. Structure-Based Design, Synthesis and Evaluation of Novel and Selective Small-Molecule Inhibitors of the Anti-Apoptotic Protein Mcl-1. [Internet] [Doctoral dissertation]. University of Michigan; 2014. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/2027.42/107109.

Council of Science Editors:

Abulwerdi FA. Structure-Based Design, Synthesis and Evaluation of Novel and Selective Small-Molecule Inhibitors of the Anti-Apoptotic Protein Mcl-1. [Doctoral Dissertation]. University of Michigan; 2014. Available from: http://hdl.handle.net/2027.42/107109


University of Cincinnati

11. Tonddast-Navaei, Sam, M.S. Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines.

Degree: PhD, Arts and Sciences: Chemistry, 2014, University of Cincinnati

 Proteins are large complex molecules that play important roles in cellular activities such as DNA replication, molecular transport, cell immunity, and regulatory activities. Based on… (more)

Subjects/Keywords: Physical Chemistry; Protein unfolding; Protein translocation; Protein degradation; ATPase; p97; Molecular Dynamics

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APA (6th Edition):

Tonddast-Navaei, Sam, M. S. (2014). Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384869946

Chicago Manual of Style (16th Edition):

Tonddast-Navaei, Sam, M S. “Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines.” 2014. Doctoral Dissertation, University of Cincinnati. Accessed June 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384869946.

MLA Handbook (7th Edition):

Tonddast-Navaei, Sam, M S. “Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines.” 2014. Web. 19 Jun 2019.

Vancouver:

Tonddast-Navaei, Sam MS. Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines. [Internet] [Doctoral dissertation]. University of Cincinnati; 2014. [cited 2019 Jun 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384869946.

Council of Science Editors:

Tonddast-Navaei, Sam MS. Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines. [Doctoral Dissertation]. University of Cincinnati; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384869946


University of North Texas

12. Barker, Andrew L. Archaeological Proteomics: Method Development and Analysis of Protein-Ceramic Binding.

Degree: 2010, University of North Texas

 The analysis of protein residues recovered from archaeological artifacts provides a unique opportunity to reveal new information about past societies. However, many scientists are currently… (more)

Subjects/Keywords: Archaeological residues; protein-ceramic interaction; protein extraction; Ceramics.; Protein binding.; Proteomics.; Archaeological chemistry.; Archaeology  – Methodology.

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APA (6th Edition):

Barker, A. L. (2010). Archaeological Proteomics: Method Development and Analysis of Protein-Ceramic Binding. (Thesis). University of North Texas. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc28392/

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):

Barker, Andrew L. “Archaeological Proteomics: Method Development and Analysis of Protein-Ceramic Binding.” 2010. Thesis, University of North Texas. Accessed June 19, 2019. https://digital.library.unt.edu/ark:/67531/metadc28392/.

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

MLA Handbook (7th Edition):

Barker, Andrew L. “Archaeological Proteomics: Method Development and Analysis of Protein-Ceramic Binding.” 2010. Web. 19 Jun 2019.

Vancouver:

Barker AL. Archaeological Proteomics: Method Development and Analysis of Protein-Ceramic Binding. [Internet] [Thesis]. University of North Texas; 2010. [cited 2019 Jun 19]. Available from: https://digital.library.unt.edu/ark:/67531/metadc28392/.

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

Council of Science Editors:

Barker AL. Archaeological Proteomics: Method Development and Analysis of Protein-Ceramic Binding. [Thesis]. University of North Texas; 2010. Available from: https://digital.library.unt.edu/ark:/67531/metadc28392/

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


University of Minnesota

13. Schenewerk, Audrey Rose. The incorporation of nitrosocyanin copper binding loop into azurin.

Degree: MS, Chemistry, 2010, University of Minnesota

University of Minnesota M.S. thesis. July 2010. Major: Chemistry. Advisor: Dr. Steven M. Berry. 1 computer file (PDF); v, 56 pages. Ill. (some col.)

Metalloprotein… (more)

Subjects/Keywords: Azurin; Copper; Protein; Metalloprotein design; Chemistry

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APA (6th Edition):

Schenewerk, A. R. (2010). The incorporation of nitrosocyanin copper binding loop into azurin. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/93640

Chicago Manual of Style (16th Edition):

Schenewerk, Audrey Rose. “The incorporation of nitrosocyanin copper binding loop into azurin.” 2010. Masters Thesis, University of Minnesota. Accessed June 19, 2019. http://purl.umn.edu/93640.

MLA Handbook (7th Edition):

Schenewerk, Audrey Rose. “The incorporation of nitrosocyanin copper binding loop into azurin.” 2010. Web. 19 Jun 2019.

Vancouver:

Schenewerk AR. The incorporation of nitrosocyanin copper binding loop into azurin. [Internet] [Masters thesis]. University of Minnesota; 2010. [cited 2019 Jun 19]. Available from: http://purl.umn.edu/93640.

Council of Science Editors:

Schenewerk AR. The incorporation of nitrosocyanin copper binding loop into azurin. [Masters Thesis]. University of Minnesota; 2010. Available from: http://purl.umn.edu/93640


University of Colorado

14. Drake, Matthew Robert. Using Chemical Synthesis to Investigate Protein Glycosylation: O-Mannosylation Site Specifically Modulates the Stability and Cellulose Binding Affinity of Family 1 Carbohydrate Binding Modules.

Degree: MS, Chemistry & Biochemistry, 2014, University of Colorado

  Lignocellulosic biomass is a massive, but largely unexploited potential source of biofuel. The underutilization of this resource stems largely from the fact that cellulose… (more)

Subjects/Keywords: Biofuel; Cellulase; Cellulose; Glycosylation; Protein; Synthesis; Chemistry

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APA (6th Edition):

Drake, M. R. (2014). Using Chemical Synthesis to Investigate Protein Glycosylation: O-Mannosylation Site Specifically Modulates the Stability and Cellulose Binding Affinity of Family 1 Carbohydrate Binding Modules. (Masters Thesis). University of Colorado. Retrieved from http://scholar.colorado.edu/chem_gradetds/3

Chicago Manual of Style (16th Edition):

Drake, Matthew Robert. “Using Chemical Synthesis to Investigate Protein Glycosylation: O-Mannosylation Site Specifically Modulates the Stability and Cellulose Binding Affinity of Family 1 Carbohydrate Binding Modules.” 2014. Masters Thesis, University of Colorado. Accessed June 19, 2019. http://scholar.colorado.edu/chem_gradetds/3.

MLA Handbook (7th Edition):

Drake, Matthew Robert. “Using Chemical Synthesis to Investigate Protein Glycosylation: O-Mannosylation Site Specifically Modulates the Stability and Cellulose Binding Affinity of Family 1 Carbohydrate Binding Modules.” 2014. Web. 19 Jun 2019.

Vancouver:

Drake MR. Using Chemical Synthesis to Investigate Protein Glycosylation: O-Mannosylation Site Specifically Modulates the Stability and Cellulose Binding Affinity of Family 1 Carbohydrate Binding Modules. [Internet] [Masters thesis]. University of Colorado; 2014. [cited 2019 Jun 19]. Available from: http://scholar.colorado.edu/chem_gradetds/3.

Council of Science Editors:

Drake MR. Using Chemical Synthesis to Investigate Protein Glycosylation: O-Mannosylation Site Specifically Modulates the Stability and Cellulose Binding Affinity of Family 1 Carbohydrate Binding Modules. [Masters Thesis]. University of Colorado; 2014. Available from: http://scholar.colorado.edu/chem_gradetds/3


University of Kansas

15. Lei, Ming. Using Lysine-Reactive Fluorescent Dye for Surface Characterization of a Monoclonal Antibody.

Degree: MA, Pharmaceutical Chemistry, 2014, University of Kansas

 The last decade has witnessed a rapid growth in the development of protein pharmaceuticals for diagnostic and therapeutic purposes. The biopharmaceutical industry increasingly demands thorough… (more)

Subjects/Keywords: Chemistry; Fluorescent; labeling; mass spectrometry; protein structure

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APA (6th Edition):

Lei, M. (2014). Using Lysine-Reactive Fluorescent Dye for Surface Characterization of a Monoclonal Antibody. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/21645

Chicago Manual of Style (16th Edition):

Lei, Ming. “Using Lysine-Reactive Fluorescent Dye for Surface Characterization of a Monoclonal Antibody.” 2014. Masters Thesis, University of Kansas. Accessed June 19, 2019. http://hdl.handle.net/1808/21645.

MLA Handbook (7th Edition):

Lei, Ming. “Using Lysine-Reactive Fluorescent Dye for Surface Characterization of a Monoclonal Antibody.” 2014. Web. 19 Jun 2019.

Vancouver:

Lei M. Using Lysine-Reactive Fluorescent Dye for Surface Characterization of a Monoclonal Antibody. [Internet] [Masters thesis]. University of Kansas; 2014. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/1808/21645.

Council of Science Editors:

Lei M. Using Lysine-Reactive Fluorescent Dye for Surface Characterization of a Monoclonal Antibody. [Masters Thesis]. University of Kansas; 2014. Available from: http://hdl.handle.net/1808/21645


Portland State University

16. Mbiya, Wilbes. Substituent Effects on Reactivity and Allergenicity of Benzoquinone.

Degree: PhD, Chemistry, 2013, Portland State University

  Benzoquinone (BQ) is an extremely potent electrophilic contact allergen that haptenates endogenous proteins through Michael addition (MA). It is also hypothesized that BQ may… (more)

Subjects/Keywords: Quinone  – Reactivity; Quinone  – Allergenicity; Protein binding; Chemistry

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APA (6th Edition):

Mbiya, W. (2013). Substituent Effects on Reactivity and Allergenicity of Benzoquinone. (Doctoral Dissertation). Portland State University. Retrieved from https://pdxscholar.library.pdx.edu/open_access_etds/1406

Chicago Manual of Style (16th Edition):

Mbiya, Wilbes. “Substituent Effects on Reactivity and Allergenicity of Benzoquinone.” 2013. Doctoral Dissertation, Portland State University. Accessed June 19, 2019. https://pdxscholar.library.pdx.edu/open_access_etds/1406.

MLA Handbook (7th Edition):

Mbiya, Wilbes. “Substituent Effects on Reactivity and Allergenicity of Benzoquinone.” 2013. Web. 19 Jun 2019.

Vancouver:

Mbiya W. Substituent Effects on Reactivity and Allergenicity of Benzoquinone. [Internet] [Doctoral dissertation]. Portland State University; 2013. [cited 2019 Jun 19]. Available from: https://pdxscholar.library.pdx.edu/open_access_etds/1406.

Council of Science Editors:

Mbiya W. Substituent Effects on Reactivity and Allergenicity of Benzoquinone. [Doctoral Dissertation]. Portland State University; 2013. Available from: https://pdxscholar.library.pdx.edu/open_access_etds/1406


Youngstown State University

17. Majeti, Jailakshmi Manasa. Structural Characteristics of Vpr Protein.

Degree: MSin Chemistry, Department of Chemistry, 2010, Youngstown State University

 Human immunodeficiency virus type 1 (HIV-1) is a retrovirus that is well known to be the causative agent for acquired immunodeficiency syndrome (AIDS). HIV-1 contains… (more)

Subjects/Keywords: Chemistry; Vpr protein; NMR; HIV; HPLC

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APA (6th Edition):

Majeti, J. M. (2010). Structural Characteristics of Vpr Protein. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1299529352

Chicago Manual of Style (16th Edition):

Majeti, Jailakshmi Manasa. “Structural Characteristics of Vpr Protein.” 2010. Masters Thesis, Youngstown State University. Accessed June 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1299529352.

MLA Handbook (7th Edition):

Majeti, Jailakshmi Manasa. “Structural Characteristics of Vpr Protein.” 2010. Web. 19 Jun 2019.

Vancouver:

Majeti JM. Structural Characteristics of Vpr Protein. [Internet] [Masters thesis]. Youngstown State University; 2010. [cited 2019 Jun 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1299529352.

Council of Science Editors:

Majeti JM. Structural Characteristics of Vpr Protein. [Masters Thesis]. Youngstown State University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1299529352


The Ohio State University

18. Jayasinha Arachchige, Rajith Madushanka. Development of New Paramagnetic Tags for Solid-State NMR Structural Studies of Natively Diamagnetic Proteins.

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

 Solid state NMR is a powerful technique, which can be used for structural and dynamic studies of complex biological macromolecules. However, the paucity of structural… (more)

Subjects/Keywords: Chemistry; paramagnetic tag , solid-state NMR , protein

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APA (6th Edition):

Jayasinha Arachchige, R. M. (2014). Development of New Paramagnetic Tags for Solid-State NMR Structural Studies of Natively Diamagnetic Proteins. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1388416184

Chicago Manual of Style (16th Edition):

Jayasinha Arachchige, Rajith Madushanka. “Development of New Paramagnetic Tags for Solid-State NMR Structural Studies of Natively Diamagnetic Proteins.” 2014. Masters Thesis, The Ohio State University. Accessed June 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1388416184.

MLA Handbook (7th Edition):

Jayasinha Arachchige, Rajith Madushanka. “Development of New Paramagnetic Tags for Solid-State NMR Structural Studies of Natively Diamagnetic Proteins.” 2014. Web. 19 Jun 2019.

Vancouver:

Jayasinha Arachchige RM. Development of New Paramagnetic Tags for Solid-State NMR Structural Studies of Natively Diamagnetic Proteins. [Internet] [Masters thesis]. The Ohio State University; 2014. [cited 2019 Jun 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1388416184.

Council of Science Editors:

Jayasinha Arachchige RM. Development of New Paramagnetic Tags for Solid-State NMR Structural Studies of Natively Diamagnetic Proteins. [Masters Thesis]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1388416184


University of California – Berkeley

19. Moore, Troy. Development of an economical and green chromatographic system for lanthanide purification and Progress toward protein-polymer hybrids from estrogen receptors for the detection and removal of organic pollutants from water.

Degree: Chemistry, 2013, University of California – Berkeley

 The expensive separation procedures necessary to produce pure metals have resulted in a small number of entities producing nearly all of global demand. Market control… (more)

Subjects/Keywords: Chemistry; chromatography; estrogen; lanthanide; polymer-protein; separation

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APA (6th Edition):

Moore, T. (2013). Development of an economical and green chromatographic system for lanthanide purification and Progress toward protein-polymer hybrids from estrogen receptors for the detection and removal of organic pollutants from water. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/82k2g071

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):

Moore, Troy. “Development of an economical and green chromatographic system for lanthanide purification and Progress toward protein-polymer hybrids from estrogen receptors for the detection and removal of organic pollutants from water.” 2013. Thesis, University of California – Berkeley. Accessed June 19, 2019. http://www.escholarship.org/uc/item/82k2g071.

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

MLA Handbook (7th Edition):

Moore, Troy. “Development of an economical and green chromatographic system for lanthanide purification and Progress toward protein-polymer hybrids from estrogen receptors for the detection and removal of organic pollutants from water.” 2013. Web. 19 Jun 2019.

Vancouver:

Moore T. Development of an economical and green chromatographic system for lanthanide purification and Progress toward protein-polymer hybrids from estrogen receptors for the detection and removal of organic pollutants from water. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2019 Jun 19]. Available from: http://www.escholarship.org/uc/item/82k2g071.

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

Council of Science Editors:

Moore T. Development of an economical and green chromatographic system for lanthanide purification and Progress toward protein-polymer hybrids from estrogen receptors for the detection and removal of organic pollutants from water. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/82k2g071

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


University of California – Santa Cruz

20. Burke, Jason R. Structural Studies of Retinoblastoma Protein Phosphorylation.

Degree: Chemistry, 2012, University of California – Santa Cruz

 The Retinoblastoma Protein (Rb) is a sentinel of the cell division process. When phosphorylated, Rb is inactivated and physically releases its protein-binding partner, E2F; a… (more)

Subjects/Keywords: Chemistry; E2F; Phosphorylation; Protein; Rb; Retinoblastoma; Structure

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APA (6th Edition):

Burke, J. R. (2012). Structural Studies of Retinoblastoma Protein Phosphorylation. (Thesis). University of California – Santa Cruz. Retrieved from http://www.escholarship.org/uc/item/58r8s5d4

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):

Burke, Jason R. “Structural Studies of Retinoblastoma Protein Phosphorylation.” 2012. Thesis, University of California – Santa Cruz. Accessed June 19, 2019. http://www.escholarship.org/uc/item/58r8s5d4.

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

MLA Handbook (7th Edition):

Burke, Jason R. “Structural Studies of Retinoblastoma Protein Phosphorylation.” 2012. Web. 19 Jun 2019.

Vancouver:

Burke JR. Structural Studies of Retinoblastoma Protein Phosphorylation. [Internet] [Thesis]. University of California – Santa Cruz; 2012. [cited 2019 Jun 19]. Available from: http://www.escholarship.org/uc/item/58r8s5d4.

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

Council of Science Editors:

Burke JR. Structural Studies of Retinoblastoma Protein Phosphorylation. [Thesis]. University of California – Santa Cruz; 2012. Available from: http://www.escholarship.org/uc/item/58r8s5d4

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


Duke University

21. Glass, Keely Elizabeth. Chemical and Physical Analysis of Melanin in Complex Biological Matrices .

Degree: 2014, Duke University

  Melanin is a ubiquitous biological pigment found in bacteria, fungi, plants, and animals. It has a diverse range of ecological and biochemical functions including… (more)

Subjects/Keywords: Chemistry; eumelanin; fossils; Jurassic; melanin; preservation; protein

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APA (6th Edition):

Glass, K. E. (2014). Chemical and Physical Analysis of Melanin in Complex Biological Matrices . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/8781

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):

Glass, Keely Elizabeth. “Chemical and Physical Analysis of Melanin in Complex Biological Matrices .” 2014. Thesis, Duke University. Accessed June 19, 2019. http://hdl.handle.net/10161/8781.

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

MLA Handbook (7th Edition):

Glass, Keely Elizabeth. “Chemical and Physical Analysis of Melanin in Complex Biological Matrices .” 2014. Web. 19 Jun 2019.

Vancouver:

Glass KE. Chemical and Physical Analysis of Melanin in Complex Biological Matrices . [Internet] [Thesis]. Duke University; 2014. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/10161/8781.

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

Council of Science Editors:

Glass KE. Chemical and Physical Analysis of Melanin in Complex Biological Matrices . [Thesis]. Duke University; 2014. Available from: http://hdl.handle.net/10161/8781

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


University of Oxford

22. Angué, Lauriane. Single molecule studies of a voltage-gated potassium channel.

Degree: PhD, 2013, University of Oxford

 This thesis aims to study the activation and deactivation mechanism of voltage-gated K+ channels (Kv), through fluorescence and electrical measurements. Transmembrane voltage changes are detected… (more)

Subjects/Keywords: 546; Molecular biophysics (biochemistry); Protein chemistry; Biophysics

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APA (6th Edition):

Angué, L. (2013). Single molecule studies of a voltage-gated potassium channel. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:21cc3408-68c0-480c-a6f2-ab04edc0963d ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.669847

Chicago Manual of Style (16th Edition):

Angué, Lauriane. “Single molecule studies of a voltage-gated potassium channel.” 2013. Doctoral Dissertation, University of Oxford. Accessed June 19, 2019. http://ora.ox.ac.uk/objects/uuid:21cc3408-68c0-480c-a6f2-ab04edc0963d ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.669847.

MLA Handbook (7th Edition):

Angué, Lauriane. “Single molecule studies of a voltage-gated potassium channel.” 2013. Web. 19 Jun 2019.

Vancouver:

Angué L. Single molecule studies of a voltage-gated potassium channel. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2019 Jun 19]. Available from: http://ora.ox.ac.uk/objects/uuid:21cc3408-68c0-480c-a6f2-ab04edc0963d ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.669847.

Council of Science Editors:

Angué L. Single molecule studies of a voltage-gated potassium channel. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:21cc3408-68c0-480c-a6f2-ab04edc0963d ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.669847

23. Jiao, Yuanfang. The development of accurate force fields for protein simulation.

Degree: PhD, Department of Chemistry, 2012, Kansas State University

 Computer simulations have provided a wealth of information concerning a wide range of systems. The precision of computer simulation results depends on the degree of… (more)

Subjects/Keywords: Protein simulation; Force field; Chemistry (0485)

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APA (6th Edition):

Jiao, Y. (2012). The development of accurate force fields for protein simulation. (Doctoral Dissertation). Kansas State University. Retrieved from http://hdl.handle.net/2097/13946

Chicago Manual of Style (16th Edition):

Jiao, Yuanfang. “The development of accurate force fields for protein simulation.” 2012. Doctoral Dissertation, Kansas State University. Accessed June 19, 2019. http://hdl.handle.net/2097/13946.

MLA Handbook (7th Edition):

Jiao, Yuanfang. “The development of accurate force fields for protein simulation.” 2012. Web. 19 Jun 2019.

Vancouver:

Jiao Y. The development of accurate force fields for protein simulation. [Internet] [Doctoral dissertation]. Kansas State University; 2012. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/2097/13946.

Council of Science Editors:

Jiao Y. The development of accurate force fields for protein simulation. [Doctoral Dissertation]. Kansas State University; 2012. Available from: http://hdl.handle.net/2097/13946


University of Minnesota

24. Schenewerk, Audrey Rose. The incorporation of nitrosocyanin copper binding loop into azurin.

Degree: MS, Chemistry, 2010, University of Minnesota

 Metalloprotein design and engineering can be used to probe our understanding of active site structure and function. Loop-directed mutagenesis has been used in the metalloprotein… (more)

Subjects/Keywords: Azurin; Copper; Protein; Metalloprotein design; Chemistry

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APA (6th Edition):

Schenewerk, A. R. (2010). The incorporation of nitrosocyanin copper binding loop into azurin. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/93640

Chicago Manual of Style (16th Edition):

Schenewerk, Audrey Rose. “The incorporation of nitrosocyanin copper binding loop into azurin.” 2010. Masters Thesis, University of Minnesota. Accessed June 19, 2019. http://purl.umn.edu/93640.

MLA Handbook (7th Edition):

Schenewerk, Audrey Rose. “The incorporation of nitrosocyanin copper binding loop into azurin.” 2010. Web. 19 Jun 2019.

Vancouver:

Schenewerk AR. The incorporation of nitrosocyanin copper binding loop into azurin. [Internet] [Masters thesis]. University of Minnesota; 2010. [cited 2019 Jun 19]. Available from: http://purl.umn.edu/93640.

Council of Science Editors:

Schenewerk AR. The incorporation of nitrosocyanin copper binding loop into azurin. [Masters Thesis]. University of Minnesota; 2010. Available from: http://purl.umn.edu/93640


University of South Carolina

25. Celeste, Lesa Rachel. The Mechanism of N10-Formyltetrahydrofolate Synthetase. Use of Human Thymidylate Synthase Variants to Characterize Asymmetric Ligand Binding and to Identify Novel Allosteric Inhibitors.

Degree: PhD, Chemistry and Biochemistry, 2012, University of South Carolina

  Part I: N10-Formyltetrahydrofolate Synthetase (FTHFS), one of several folate enzymes, catalyzes the conversion of tetrahydrofolate (THF) to N10-formyltetrahydrofolate (fTHF) in an ATP dependent manner.… (more)

Subjects/Keywords: Chemistry; Physical Sciences and Mathematics; Protein Crystallography

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APA (6th Edition):

Celeste, L. R. (2012). The Mechanism of N10-Formyltetrahydrofolate Synthetase. Use of Human Thymidylate Synthase Variants to Characterize Asymmetric Ligand Binding and to Identify Novel Allosteric Inhibitors. (Doctoral Dissertation). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/664

Chicago Manual of Style (16th Edition):

Celeste, Lesa Rachel. “The Mechanism of N10-Formyltetrahydrofolate Synthetase. Use of Human Thymidylate Synthase Variants to Characterize Asymmetric Ligand Binding and to Identify Novel Allosteric Inhibitors.” 2012. Doctoral Dissertation, University of South Carolina. Accessed June 19, 2019. https://scholarcommons.sc.edu/etd/664.

MLA Handbook (7th Edition):

Celeste, Lesa Rachel. “The Mechanism of N10-Formyltetrahydrofolate Synthetase. Use of Human Thymidylate Synthase Variants to Characterize Asymmetric Ligand Binding and to Identify Novel Allosteric Inhibitors.” 2012. Web. 19 Jun 2019.

Vancouver:

Celeste LR. The Mechanism of N10-Formyltetrahydrofolate Synthetase. Use of Human Thymidylate Synthase Variants to Characterize Asymmetric Ligand Binding and to Identify Novel Allosteric Inhibitors. [Internet] [Doctoral dissertation]. University of South Carolina; 2012. [cited 2019 Jun 19]. Available from: https://scholarcommons.sc.edu/etd/664.

Council of Science Editors:

Celeste LR. The Mechanism of N10-Formyltetrahydrofolate Synthetase. Use of Human Thymidylate Synthase Variants to Characterize Asymmetric Ligand Binding and to Identify Novel Allosteric Inhibitors. [Doctoral Dissertation]. University of South Carolina; 2012. Available from: https://scholarcommons.sc.edu/etd/664

26. Witkowski, Witold Andrej. Caspase-7 Loop Conformations as a Means of Allosteric Control.

Degree: PhD, Chemistry, 2011, U of Massachusetts : PhD

  The caspase family of proteins is critical to biological understanding, because they serve as the final arbiters of life and death, being the initiators… (more)

Subjects/Keywords: Apoptosis; Caspase; Crystallography; Protein Redesign; Chemistry

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APA (6th Edition):

Witkowski, W. A. (2011). Caspase-7 Loop Conformations as a Means of Allosteric Control. (Doctoral Dissertation). U of Massachusetts : PhD. Retrieved from https://scholarworks.umass.edu/open_access_dissertations/405

Chicago Manual of Style (16th Edition):

Witkowski, Witold Andrej. “Caspase-7 Loop Conformations as a Means of Allosteric Control.” 2011. Doctoral Dissertation, U of Massachusetts : PhD. Accessed June 19, 2019. https://scholarworks.umass.edu/open_access_dissertations/405.

MLA Handbook (7th Edition):

Witkowski, Witold Andrej. “Caspase-7 Loop Conformations as a Means of Allosteric Control.” 2011. Web. 19 Jun 2019.

Vancouver:

Witkowski WA. Caspase-7 Loop Conformations as a Means of Allosteric Control. [Internet] [Doctoral dissertation]. U of Massachusetts : PhD; 2011. [cited 2019 Jun 19]. Available from: https://scholarworks.umass.edu/open_access_dissertations/405.

Council of Science Editors:

Witkowski WA. Caspase-7 Loop Conformations as a Means of Allosteric Control. [Doctoral Dissertation]. U of Massachusetts : PhD; 2011. Available from: https://scholarworks.umass.edu/open_access_dissertations/405


University of Arizona

27. Egas Proaño, David Alexis. Colloidal Silica as a Platform for Trace Protein Analysis and Recovery .

Degree: 2011, University of Arizona

 Early intervention in cancer and other illnesses is highly desired. The evolution of the proteomics field has benefited the possibility of getting to this goal… (more)

Subjects/Keywords: Recovery; Silica; Trace; Chemistry; Colloidal; Protein

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APA (6th Edition):

Egas Proaño, D. A. (2011). Colloidal Silica as a Platform for Trace Protein Analysis and Recovery . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/202703

Chicago Manual of Style (16th Edition):

Egas Proaño, David Alexis. “Colloidal Silica as a Platform for Trace Protein Analysis and Recovery .” 2011. Doctoral Dissertation, University of Arizona. Accessed June 19, 2019. http://hdl.handle.net/10150/202703.

MLA Handbook (7th Edition):

Egas Proaño, David Alexis. “Colloidal Silica as a Platform for Trace Protein Analysis and Recovery .” 2011. Web. 19 Jun 2019.

Vancouver:

Egas Proaño DA. Colloidal Silica as a Platform for Trace Protein Analysis and Recovery . [Internet] [Doctoral dissertation]. University of Arizona; 2011. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/10150/202703.

Council of Science Editors:

Egas Proaño DA. Colloidal Silica as a Platform for Trace Protein Analysis and Recovery . [Doctoral Dissertation]. University of Arizona; 2011. Available from: http://hdl.handle.net/10150/202703


University of Arizona

28. Lamba, Vandana. Development of Potent and Selective Bivalent Inhibitors for Protein Kinases Utilizing Phage Display .

Degree: 2012, University of Arizona

Protein kinases function as key regulators in a variety of signaling pathways by executing the phosphorylation of a variety of protein substrates. Perturbation in the… (more)

Subjects/Keywords: Protein Kinases; Chemistry; Bivalent Inhibitors; Phage Display

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APA (6th Edition):

Lamba, V. (2012). Development of Potent and Selective Bivalent Inhibitors for Protein Kinases Utilizing Phage Display . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/265559

Chicago Manual of Style (16th Edition):

Lamba, Vandana. “Development of Potent and Selective Bivalent Inhibitors for Protein Kinases Utilizing Phage Display .” 2012. Doctoral Dissertation, University of Arizona. Accessed June 19, 2019. http://hdl.handle.net/10150/265559.

MLA Handbook (7th Edition):

Lamba, Vandana. “Development of Potent and Selective Bivalent Inhibitors for Protein Kinases Utilizing Phage Display .” 2012. Web. 19 Jun 2019.

Vancouver:

Lamba V. Development of Potent and Selective Bivalent Inhibitors for Protein Kinases Utilizing Phage Display . [Internet] [Doctoral dissertation]. University of Arizona; 2012. [cited 2019 Jun 19]. Available from: http://hdl.handle.net/10150/265559.

Council of Science Editors:

Lamba V. Development of Potent and Selective Bivalent Inhibitors for Protein Kinases Utilizing Phage Display . [Doctoral Dissertation]. University of Arizona; 2012. Available from: http://hdl.handle.net/10150/265559

29. Mythili, J Krishna. Identification of a fluorescent protein from a marine Zoanthid: Zoanthus Sansibaricus (Carlgren) from the intertidal rocky shore of Anjuna (Goa); -.

Degree: Pharmacy, 2011, Jawaharlal Nehru Technological University

Zoanthids comprise an order of benthic, generally colonial Cnidarians, which can usually be distinguished from other hexacorallians by embedded sand and detritus in their mesoglea.… (more)

Subjects/Keywords: Green Fluorescent Protein; Chemistry; Protein; Zoanthid Taxonomy; Pharmacy

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

APA (6th Edition):

Mythili, J. K. (2011). Identification of a fluorescent protein from a marine Zoanthid: Zoanthus Sansibaricus (Carlgren) from the intertidal rocky shore of Anjuna (Goa); -. (Thesis). Jawaharlal Nehru Technological University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/4505

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):

Mythili, J Krishna. “Identification of a fluorescent protein from a marine Zoanthid: Zoanthus Sansibaricus (Carlgren) from the intertidal rocky shore of Anjuna (Goa); -.” 2011. Thesis, Jawaharlal Nehru Technological University. Accessed June 19, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/4505.

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

MLA Handbook (7th Edition):

Mythili, J Krishna. “Identification of a fluorescent protein from a marine Zoanthid: Zoanthus Sansibaricus (Carlgren) from the intertidal rocky shore of Anjuna (Goa); -.” 2011. Web. 19 Jun 2019.

Vancouver:

Mythili JK. Identification of a fluorescent protein from a marine Zoanthid: Zoanthus Sansibaricus (Carlgren) from the intertidal rocky shore of Anjuna (Goa); -. [Internet] [Thesis]. Jawaharlal Nehru Technological University; 2011. [cited 2019 Jun 19]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/4505.

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

Council of Science Editors:

Mythili JK. Identification of a fluorescent protein from a marine Zoanthid: Zoanthus Sansibaricus (Carlgren) from the intertidal rocky shore of Anjuna (Goa); -. [Thesis]. Jawaharlal Nehru Technological University; 2011. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/4505

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


University of Cincinnati

30. Kravats, Andrea N. Coarse grained molecular dynamics simulations of the coupling between the allosteric mechanism of the ClpY nanomachine and threading of a substrate protein.

Degree: PhD, Arts and Sciences: Chemistry, 2013, University of Cincinnati

Protein quality control is critical in maintaining cell viability. Recognitionand degradation of aberrant proteins in the cellular environment is essential,as many neurodegenerative diseases are linked… (more)

Subjects/Keywords: Physical Chemistry; ATPase; protein unfolding; protein translocation; coarse grained simulations

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

APA (6th Edition):

Kravats, A. N. (2013). Coarse grained molecular dynamics simulations of the coupling between the allosteric mechanism of the ClpY nanomachine and threading of a substrate protein. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384849649

Chicago Manual of Style (16th Edition):

Kravats, Andrea N. “Coarse grained molecular dynamics simulations of the coupling between the allosteric mechanism of the ClpY nanomachine and threading of a substrate protein.” 2013. Doctoral Dissertation, University of Cincinnati. Accessed June 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384849649.

MLA Handbook (7th Edition):

Kravats, Andrea N. “Coarse grained molecular dynamics simulations of the coupling between the allosteric mechanism of the ClpY nanomachine and threading of a substrate protein.” 2013. Web. 19 Jun 2019.

Vancouver:

Kravats AN. Coarse grained molecular dynamics simulations of the coupling between the allosteric mechanism of the ClpY nanomachine and threading of a substrate protein. [Internet] [Doctoral dissertation]. University of Cincinnati; 2013. [cited 2019 Jun 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384849649.

Council of Science Editors:

Kravats AN. Coarse grained molecular dynamics simulations of the coupling between the allosteric mechanism of the ClpY nanomachine and threading of a substrate protein. [Doctoral Dissertation]. University of Cincinnati; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384849649

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