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You searched for subject:(Rop Rosetta protein G combinatorial library hydrophobic core library computational design high throughput). Showing records 1 – 30 of 116810 total matches.

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The Ohio State University

1. Li, Weiyi. Protein Engineering Hydrophobic Core Residues of Computationally Designed Protein G and Single-Chain Rop: Investigating the Relationship between Protein Primary structure and Protein Stability through High-Throughput Approaches.

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

 The sequence-structure-stability relationship is a key problem in the field of protein science. Although a large amount of research has been working on it in… (more)

Subjects/Keywords: Biochemistry; Chemistry; Biophysics; Biology; Rop, Rosetta, protein G, combinatorial library, hydrophobic core library, computational design, high-throughput

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APA (6th Edition):

Li, W. (2014). Protein Engineering Hydrophobic Core Residues of Computationally Designed Protein G and Single-Chain Rop: Investigating the Relationship between Protein Primary structure and Protein Stability through High-Throughput Approaches. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1398956266

Chicago Manual of Style (16th Edition):

Li, Weiyi. “Protein Engineering Hydrophobic Core Residues of Computationally Designed Protein G and Single-Chain Rop: Investigating the Relationship between Protein Primary structure and Protein Stability through High-Throughput Approaches.” 2014. Masters Thesis, The Ohio State University. Accessed August 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1398956266.

MLA Handbook (7th Edition):

Li, Weiyi. “Protein Engineering Hydrophobic Core Residues of Computationally Designed Protein G and Single-Chain Rop: Investigating the Relationship between Protein Primary structure and Protein Stability through High-Throughput Approaches.” 2014. Web. 22 Aug 2019.

Vancouver:

Li W. Protein Engineering Hydrophobic Core Residues of Computationally Designed Protein G and Single-Chain Rop: Investigating the Relationship between Protein Primary structure and Protein Stability through High-Throughput Approaches. [Internet] [Masters thesis]. The Ohio State University; 2014. [cited 2019 Aug 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1398956266.

Council of Science Editors:

Li W. Protein Engineering Hydrophobic Core Residues of Computationally Designed Protein G and Single-Chain Rop: Investigating the Relationship between Protein Primary structure and Protein Stability through High-Throughput Approaches. [Masters Thesis]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1398956266


The Ohio State University

2. Sen, Shiladitya. Engineering Proteins for Enhanced Stability using High-throughput and Combinatorial methods.

Degree: PhD, Chemistry, 2013, The Ohio State University

 The inability to accurately decipher the relationship between a protein’s sequence and its structural stability presents a major difficulty in predicting the effects of mutation… (more)

Subjects/Keywords: Chemistry; Biochemistry; Protein engineering, High-throughput, Stability, Combinatorial library,Antibodies

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APA (6th Edition):

Sen, S. (2013). Engineering Proteins for Enhanced Stability using High-throughput and Combinatorial methods. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1385987653

Chicago Manual of Style (16th Edition):

Sen, Shiladitya. “Engineering Proteins for Enhanced Stability using High-throughput and Combinatorial methods.” 2013. Doctoral Dissertation, The Ohio State University. Accessed August 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1385987653.

MLA Handbook (7th Edition):

Sen, Shiladitya. “Engineering Proteins for Enhanced Stability using High-throughput and Combinatorial methods.” 2013. Web. 22 Aug 2019.

Vancouver:

Sen S. Engineering Proteins for Enhanced Stability using High-throughput and Combinatorial methods. [Internet] [Doctoral dissertation]. The Ohio State University; 2013. [cited 2019 Aug 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1385987653.

Council of Science Editors:

Sen S. Engineering Proteins for Enhanced Stability using High-throughput and Combinatorial methods. [Doctoral Dissertation]. The Ohio State University; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1385987653


Cornell University

3. Wong, Sharon. Probing the biophysical mechanisms of gene delivery by synthetic evolution of combinatorial polymeric vector libraries .

Degree: 2008, Cornell University

 The prospect of treating debilitating and even fatal diseases by way of genetic-based interventions has been the long-standing goal of gene therapy. However, its widespread… (more)

Subjects/Keywords: gene delivery; polymeric vectors; combinatorial library; high throughput

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APA (6th Edition):

Wong, S. (2008). Probing the biophysical mechanisms of gene delivery by synthetic evolution of combinatorial polymeric vector libraries . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/10868

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):

Wong, Sharon. “Probing the biophysical mechanisms of gene delivery by synthetic evolution of combinatorial polymeric vector libraries .” 2008. Thesis, Cornell University. Accessed August 22, 2019. http://hdl.handle.net/1813/10868.

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

MLA Handbook (7th Edition):

Wong, Sharon. “Probing the biophysical mechanisms of gene delivery by synthetic evolution of combinatorial polymeric vector libraries .” 2008. Web. 22 Aug 2019.

Vancouver:

Wong S. Probing the biophysical mechanisms of gene delivery by synthetic evolution of combinatorial polymeric vector libraries . [Internet] [Thesis]. Cornell University; 2008. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1813/10868.

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

Council of Science Editors:

Wong S. Probing the biophysical mechanisms of gene delivery by synthetic evolution of combinatorial polymeric vector libraries . [Thesis]. Cornell University; 2008. Available from: http://hdl.handle.net/1813/10868

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


Vanderbilt University

4. Morin, Andrew. The computational design of protein-ligand interfaces.

Degree: PhD, Chemical and Physical Biology, 2011, Vanderbilt University

 ANDREW MORIN Dissertation under the direction of Professor Jens Meiler. Interaction between protein and ligand is a fundamental mechanism in biology. The goal of my… (more)

Subjects/Keywords: computational protein design; Rosetta; ligand interface

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APA (6th Edition):

Morin, A. (2011). The computational design of protein-ligand interfaces. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-05182011-125917/ ;

Chicago Manual of Style (16th Edition):

Morin, Andrew. “The computational design of protein-ligand interfaces.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed August 22, 2019. http://etd.library.vanderbilt.edu/available/etd-05182011-125917/ ;.

MLA Handbook (7th Edition):

Morin, Andrew. “The computational design of protein-ligand interfaces.” 2011. Web. 22 Aug 2019.

Vancouver:

Morin A. The computational design of protein-ligand interfaces. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2019 Aug 22]. Available from: http://etd.library.vanderbilt.edu/available/etd-05182011-125917/ ;.

Council of Science Editors:

Morin A. The computational design of protein-ligand interfaces. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://etd.library.vanderbilt.edu/available/etd-05182011-125917/ ;


University of Kansas

5. Imaduwage, Kasun Prabodha. High-Throughput Screening (HTS) of Potential Lead Compounds for Target Proteins with No False Identifications Using LC/MS.

Degree: PhD, Chemistry, 2017, University of Kansas

 Developing effective high throughput screening (HTS) methods is of paramount importance in the early stage of drug discovery. When a protein binding event can be… (more)

Subjects/Keywords: Chemistry; false negatives; false positives; High throughput screening; LC/MS; library compounds; Target protein

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APA (6th Edition):

Imaduwage, K. P. (2017). High-Throughput Screening (HTS) of Potential Lead Compounds for Target Proteins with No False Identifications Using LC/MS. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/26012

Chicago Manual of Style (16th Edition):

Imaduwage, Kasun Prabodha. “High-Throughput Screening (HTS) of Potential Lead Compounds for Target Proteins with No False Identifications Using LC/MS.” 2017. Doctoral Dissertation, University of Kansas. Accessed August 22, 2019. http://hdl.handle.net/1808/26012.

MLA Handbook (7th Edition):

Imaduwage, Kasun Prabodha. “High-Throughput Screening (HTS) of Potential Lead Compounds for Target Proteins with No False Identifications Using LC/MS.” 2017. Web. 22 Aug 2019.

Vancouver:

Imaduwage KP. High-Throughput Screening (HTS) of Potential Lead Compounds for Target Proteins with No False Identifications Using LC/MS. [Internet] [Doctoral dissertation]. University of Kansas; 2017. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1808/26012.

Council of Science Editors:

Imaduwage KP. High-Throughput Screening (HTS) of Potential Lead Compounds for Target Proteins with No False Identifications Using LC/MS. [Doctoral Dissertation]. University of Kansas; 2017. Available from: http://hdl.handle.net/1808/26012


University of Minnesota

6. Woldring, Daniel. Constrained Diversification Enhances Protein Ligand Discovery and Evolution.

Degree: PhD, Chemical Engineering, 2017, University of Minnesota

 Engineered proteins have strongly benefited the effectiveness and variety of precision drugs, molecular diagnostic agents, and fundamental research reagents. A growing demand for new therapeutics… (more)

Subjects/Keywords: computational biology; deep sequencing; library design; protein engineering; protein-protein interaction; stability engineering

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APA (6th Edition):

Woldring, D. (2017). Constrained Diversification Enhances Protein Ligand Discovery and Evolution. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/191350

Chicago Manual of Style (16th Edition):

Woldring, Daniel. “Constrained Diversification Enhances Protein Ligand Discovery and Evolution.” 2017. Doctoral Dissertation, University of Minnesota. Accessed August 22, 2019. http://hdl.handle.net/11299/191350.

MLA Handbook (7th Edition):

Woldring, Daniel. “Constrained Diversification Enhances Protein Ligand Discovery and Evolution.” 2017. Web. 22 Aug 2019.

Vancouver:

Woldring D. Constrained Diversification Enhances Protein Ligand Discovery and Evolution. [Internet] [Doctoral dissertation]. University of Minnesota; 2017. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/11299/191350.

Council of Science Editors:

Woldring D. Constrained Diversification Enhances Protein Ligand Discovery and Evolution. [Doctoral Dissertation]. University of Minnesota; 2017. Available from: http://hdl.handle.net/11299/191350


University of Pennsylvania

7. Brey, Darren M. Combinatorial Polymer Synthesis and High-Throughput Screening Technology to Identify Optimal Approaches for Mineralized Tissue Engineering.

Degree: 2010, University of Pennsylvania

 The general tissue engineering approach is to combine cells, scaffolding, and signaling molecules in a manner that treats damaged or diseased tissues. Progress in the… (more)

Subjects/Keywords: combinatorial library; high-throughput screening; mesenchymal stem cells; mineralization; bone tissue engineering; Biomaterials; Molecular, Cellular, and Tissue Engineering

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APA (6th Edition):

Brey, D. M. (2010). Combinatorial Polymer Synthesis and High-Throughput Screening Technology to Identify Optimal Approaches for Mineralized Tissue Engineering. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/230

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):

Brey, Darren M. “Combinatorial Polymer Synthesis and High-Throughput Screening Technology to Identify Optimal Approaches for Mineralized Tissue Engineering.” 2010. Thesis, University of Pennsylvania. Accessed August 22, 2019. https://repository.upenn.edu/edissertations/230.

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

MLA Handbook (7th Edition):

Brey, Darren M. “Combinatorial Polymer Synthesis and High-Throughput Screening Technology to Identify Optimal Approaches for Mineralized Tissue Engineering.” 2010. Web. 22 Aug 2019.

Vancouver:

Brey DM. Combinatorial Polymer Synthesis and High-Throughput Screening Technology to Identify Optimal Approaches for Mineralized Tissue Engineering. [Internet] [Thesis]. University of Pennsylvania; 2010. [cited 2019 Aug 22]. Available from: https://repository.upenn.edu/edissertations/230.

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

Council of Science Editors:

Brey DM. Combinatorial Polymer Synthesis and High-Throughput Screening Technology to Identify Optimal Approaches for Mineralized Tissue Engineering. [Thesis]. University of Pennsylvania; 2010. Available from: https://repository.upenn.edu/edissertations/230

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


University of Washington

8. Basanta, Benjamin. Beyond single-protein de novo design: A generative algorithm for the NTF2-like superfamily.

Degree: PhD, 2019, University of Washington

 Natural proteins evolved over billions of years to regulate cellular growth, ward off infection and capture and store solar energy. Proteins thus serve as the… (more)

Subjects/Keywords: Computational Biology; generative algorithm; generative design; High-throughput screening; Protein design; Biochemistry; Biological chemistry

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APA (6th Edition):

Basanta, B. (2019). Beyond single-protein de novo design: A generative algorithm for the NTF2-like superfamily. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/43640

Chicago Manual of Style (16th Edition):

Basanta, Benjamin. “Beyond single-protein de novo design: A generative algorithm for the NTF2-like superfamily.” 2019. Doctoral Dissertation, University of Washington. Accessed August 22, 2019. http://hdl.handle.net/1773/43640.

MLA Handbook (7th Edition):

Basanta, Benjamin. “Beyond single-protein de novo design: A generative algorithm for the NTF2-like superfamily.” 2019. Web. 22 Aug 2019.

Vancouver:

Basanta B. Beyond single-protein de novo design: A generative algorithm for the NTF2-like superfamily. [Internet] [Doctoral dissertation]. University of Washington; 2019. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1773/43640.

Council of Science Editors:

Basanta B. Beyond single-protein de novo design: A generative algorithm for the NTF2-like superfamily. [Doctoral Dissertation]. University of Washington; 2019. Available from: http://hdl.handle.net/1773/43640


University of Washington

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

Degree: PhD, 2015, University of Washington

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Yu, Shawn. “Computational design of interleukin-2 mimetics.” 2015. Doctoral Dissertation, University of Washington. Accessed August 22, 2019. http://hdl.handle.net/1773/33593.

MLA Handbook (7th Edition):

Yu, Shawn. “Computational design of interleukin-2 mimetics.” 2015. Web. 22 Aug 2019.

Vancouver:

Yu S. Computational design of interleukin-2 mimetics. [Internet] [Doctoral dissertation]. University of Washington; 2015. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1773/33593.

Council of Science Editors:

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


Texas A&M University

10. Haynes, Abria R. Characterization of Extremophilic Bacteria for Potential in the Biofuel and Bioprocess Industries.

Degree: 2014, Texas A&M University

 Industrial bioprocesses are constrained by the availability of microbes that are optimized for harsh bioprocess conditions. Over 500 soil and sediment samples collected from 77… (more)

Subjects/Keywords: Bacillus; High-Throughput Screening; Biofuels; Bacterial Library; Environmental Isolates

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APA (6th Edition):

Haynes, A. R. (2014). Characterization of Extremophilic Bacteria for Potential in the Biofuel and Bioprocess Industries. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/152602

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):

Haynes, Abria R. “Characterization of Extremophilic Bacteria for Potential in the Biofuel and Bioprocess Industries.” 2014. Thesis, Texas A&M University. Accessed August 22, 2019. http://hdl.handle.net/1969.1/152602.

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

MLA Handbook (7th Edition):

Haynes, Abria R. “Characterization of Extremophilic Bacteria for Potential in the Biofuel and Bioprocess Industries.” 2014. Web. 22 Aug 2019.

Vancouver:

Haynes AR. Characterization of Extremophilic Bacteria for Potential in the Biofuel and Bioprocess Industries. [Internet] [Thesis]. Texas A&M University; 2014. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1969.1/152602.

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

Council of Science Editors:

Haynes AR. Characterization of Extremophilic Bacteria for Potential in the Biofuel and Bioprocess Industries. [Thesis]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/152602

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


Vanderbilt University

11. Allison, Brittany Ann. Computational Design of Protein-Ligand Interfaces Using RosettaLigand.

Degree: PhD, Chemistry, 2016, Vanderbilt University

Computational design of protein-ligand interfaces expands understanding of the basic forces involved in molecular recognition, and also contributes to the development of protein therapeutics. My… (more)

Subjects/Keywords: protein engineering; protein ligand binding; RosettaLigand; Rosetta; protein small molecule interactions; interface design; computational design; ligand macromolecule recognition; NMR; binding affinity

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APA (6th Edition):

Allison, B. A. (2016). Computational Design of Protein-Ligand Interfaces Using RosettaLigand. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-03282016-022145/ ;

Chicago Manual of Style (16th Edition):

Allison, Brittany Ann. “Computational Design of Protein-Ligand Interfaces Using RosettaLigand.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed August 22, 2019. http://etd.library.vanderbilt.edu/available/etd-03282016-022145/ ;.

MLA Handbook (7th Edition):

Allison, Brittany Ann. “Computational Design of Protein-Ligand Interfaces Using RosettaLigand.” 2016. Web. 22 Aug 2019.

Vancouver:

Allison BA. Computational Design of Protein-Ligand Interfaces Using RosettaLigand. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2019 Aug 22]. Available from: http://etd.library.vanderbilt.edu/available/etd-03282016-022145/ ;.

Council of Science Editors:

Allison BA. Computational Design of Protein-Ligand Interfaces Using RosettaLigand. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://etd.library.vanderbilt.edu/available/etd-03282016-022145/ ;

12. Heyer, Erin E. Optimizing RNA Library Preparation to Redefine the Translational Status of 80S Monosomes: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, RNA Therapeutics Institute, 2015, U of Massachusetts : Med

  Deep sequencing of strand-specific cDNA libraries is now a ubiquitous tool for identifying and quantifying RNAs in diverse sample types. The accuracy of conclusions… (more)

Subjects/Keywords: High-Throughput Nucleotide Sequencing; Nucleotides; RNA; Gene Library; Open Reading Frames; Biochemistry; Bioinformatics; Cell Biology; Computational Biology; Genetics; Molecular Biology; Molecular Genetics

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APA (6th Edition):

Heyer, E. E. (2015). Optimizing RNA Library Preparation to Redefine the Translational Status of 80S Monosomes: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/810

Chicago Manual of Style (16th Edition):

Heyer, Erin E. “Optimizing RNA Library Preparation to Redefine the Translational Status of 80S Monosomes: A Dissertation.” 2015. Doctoral Dissertation, U of Massachusetts : Med. Accessed August 22, 2019. http://escholarship.umassmed.edu/gsbs_diss/810.

MLA Handbook (7th Edition):

Heyer, Erin E. “Optimizing RNA Library Preparation to Redefine the Translational Status of 80S Monosomes: A Dissertation.” 2015. Web. 22 Aug 2019.

Vancouver:

Heyer EE. Optimizing RNA Library Preparation to Redefine the Translational Status of 80S Monosomes: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2015. [cited 2019 Aug 22]. Available from: http://escholarship.umassmed.edu/gsbs_diss/810.

Council of Science Editors:

Heyer EE. Optimizing RNA Library Preparation to Redefine the Translational Status of 80S Monosomes: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2015. Available from: http://escholarship.umassmed.edu/gsbs_diss/810

13. Lokits, Alyssa Dawn. Nuthin' but a G (protein) thang: Insights into the Mechanics of G protein Signaling from Sequence and Structure.

Degree: PhD, Neuroscience, 2017, Vanderbilt University

G protein-coupled receptors (GPCRs) are a large and diverse group of transmembrane receptors which convert extracellular signals into intracellular responses via coupling to heterotrimeric G(more)

Subjects/Keywords: G protein; G protein Coupled Receptor; GPCR; structure; computation; evolution; phylogenetics; thermodynamics; G alpha; Rosetta

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APA (6th Edition):

Lokits, A. D. (2017). Nuthin' but a G (protein) thang: Insights into the Mechanics of G protein Signaling from Sequence and Structure. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-06132017-085149/ ;

Chicago Manual of Style (16th Edition):

Lokits, Alyssa Dawn. “Nuthin' but a G (protein) thang: Insights into the Mechanics of G protein Signaling from Sequence and Structure.” 2017. Doctoral Dissertation, Vanderbilt University. Accessed August 22, 2019. http://etd.library.vanderbilt.edu/available/etd-06132017-085149/ ;.

MLA Handbook (7th Edition):

Lokits, Alyssa Dawn. “Nuthin' but a G (protein) thang: Insights into the Mechanics of G protein Signaling from Sequence and Structure.” 2017. Web. 22 Aug 2019.

Vancouver:

Lokits AD. Nuthin' but a G (protein) thang: Insights into the Mechanics of G protein Signaling from Sequence and Structure. [Internet] [Doctoral dissertation]. Vanderbilt University; 2017. [cited 2019 Aug 22]. Available from: http://etd.library.vanderbilt.edu/available/etd-06132017-085149/ ;.

Council of Science Editors:

Lokits AD. Nuthin' but a G (protein) thang: Insights into the Mechanics of G protein Signaling from Sequence and Structure. [Doctoral Dissertation]. Vanderbilt University; 2017. Available from: http://etd.library.vanderbilt.edu/available/etd-06132017-085149/ ;


Vanderbilt University

14. Bender, Brian Joseph. Knowledge-Based Modeling of G-Protein Coupled Receptors and their Binding Partners.

Degree: PhD, Pharmacology, 2019, Vanderbilt University

G-protein coupled receptors (GPCRs) represent the largest family of membrane proteins and the most heavily targeted classes of proteins for therapeutic intervention. Relatively little is… (more)

Subjects/Keywords: protein modeling; rosetta; peptide docking; g-protein coupled receptors; ligand docking

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APA (6th Edition):

Bender, B. J. (2019). Knowledge-Based Modeling of G-Protein Coupled Receptors and their Binding Partners. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-01172019-103123/ ;

Chicago Manual of Style (16th Edition):

Bender, Brian Joseph. “Knowledge-Based Modeling of G-Protein Coupled Receptors and their Binding Partners.” 2019. Doctoral Dissertation, Vanderbilt University. Accessed August 22, 2019. http://etd.library.vanderbilt.edu/available/etd-01172019-103123/ ;.

MLA Handbook (7th Edition):

Bender, Brian Joseph. “Knowledge-Based Modeling of G-Protein Coupled Receptors and their Binding Partners.” 2019. Web. 22 Aug 2019.

Vancouver:

Bender BJ. Knowledge-Based Modeling of G-Protein Coupled Receptors and their Binding Partners. [Internet] [Doctoral dissertation]. Vanderbilt University; 2019. [cited 2019 Aug 22]. Available from: http://etd.library.vanderbilt.edu/available/etd-01172019-103123/ ;.

Council of Science Editors:

Bender BJ. Knowledge-Based Modeling of G-Protein Coupled Receptors and their Binding Partners. [Doctoral Dissertation]. Vanderbilt University; 2019. Available from: http://etd.library.vanderbilt.edu/available/etd-01172019-103123/ ;


University of Iowa

15. Bodle, Christopher Ralph. Identification of small molecule inhibitors of regulator of G protein signaling proteins for pretherapeutic development for treatment of multiple pathologies.

Degree: PhD, Medicinal and Natural Products Chemistry, 2017, University of Iowa

  Regulator of G-protein Signaling (RGS) proteins temporally regulate the G protein signaling cascades initiated by GPCR activation. Reports have established dysregulation of RGS expression… (more)

Subjects/Keywords: Alcoholism; Cancer; Depression; G protein; High Throughput Screening; RGS; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Bodle, C. R. (2017). Identification of small molecule inhibitors of regulator of G protein signaling proteins for pretherapeutic development for treatment of multiple pathologies. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/5420

Chicago Manual of Style (16th Edition):

Bodle, Christopher Ralph. “Identification of small molecule inhibitors of regulator of G protein signaling proteins for pretherapeutic development for treatment of multiple pathologies.” 2017. Doctoral Dissertation, University of Iowa. Accessed August 22, 2019. https://ir.uiowa.edu/etd/5420.

MLA Handbook (7th Edition):

Bodle, Christopher Ralph. “Identification of small molecule inhibitors of regulator of G protein signaling proteins for pretherapeutic development for treatment of multiple pathologies.” 2017. Web. 22 Aug 2019.

Vancouver:

Bodle CR. Identification of small molecule inhibitors of regulator of G protein signaling proteins for pretherapeutic development for treatment of multiple pathologies. [Internet] [Doctoral dissertation]. University of Iowa; 2017. [cited 2019 Aug 22]. Available from: https://ir.uiowa.edu/etd/5420.

Council of Science Editors:

Bodle CR. Identification of small molecule inhibitors of regulator of G protein signaling proteins for pretherapeutic development for treatment of multiple pathologies. [Doctoral Dissertation]. University of Iowa; 2017. Available from: https://ir.uiowa.edu/etd/5420

16. Hallen, Mark Andrew. Protein and Drug Design Algorithms Using Improved Biophysical Modeling .

Degree: 2016, Duke University

  This thesis focuses on the development of algorithms that will allow protein design calculations to incorporate more realistic modeling assumptions. Protein design algorithms search… (more)

Subjects/Keywords: Computer science; Biochemistry; Algorithms; Bioinformatics; Combinatorial optimization; Computational biology; Drug design; Protein design

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APA (6th Edition):

Hallen, M. A. (2016). Protein and Drug Design Algorithms Using Improved Biophysical Modeling . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/12120

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):

Hallen, Mark Andrew. “Protein and Drug Design Algorithms Using Improved Biophysical Modeling .” 2016. Thesis, Duke University. Accessed August 22, 2019. http://hdl.handle.net/10161/12120.

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

MLA Handbook (7th Edition):

Hallen, Mark Andrew. “Protein and Drug Design Algorithms Using Improved Biophysical Modeling .” 2016. Web. 22 Aug 2019.

Vancouver:

Hallen MA. Protein and Drug Design Algorithms Using Improved Biophysical Modeling . [Internet] [Thesis]. Duke University; 2016. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/10161/12120.

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

Council of Science Editors:

Hallen MA. Protein and Drug Design Algorithms Using Improved Biophysical Modeling . [Thesis]. Duke University; 2016. Available from: http://hdl.handle.net/10161/12120

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


Cranfield University

17. Hutchings, K D. High throughput combinatorial screening of Cu-Zn-Sn-S thin film libraries for the application of Cu2ZnSnS4 photovoltaic cells.

Degree: PhD, 2014, Cranfield University

 The naturally occurring mineral of Cu2ZnSnS4 (CZTS) is a promising alternative absorber layer for thin film based photovoltaic devices. It has the remarkable advantage that… (more)

Subjects/Keywords: Photovoltaic cells; Thin films; Dynamic combinatorial library

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APA (6th Edition):

Hutchings, K. D. (2014). High throughput combinatorial screening of Cu-Zn-Sn-S thin film libraries for the application of Cu2ZnSnS4 photovoltaic cells. (Doctoral Dissertation). Cranfield University. Retrieved from http://dspace.lib.cranfield.ac.uk/handle/1826/8771

Chicago Manual of Style (16th Edition):

Hutchings, K D. “High throughput combinatorial screening of Cu-Zn-Sn-S thin film libraries for the application of Cu2ZnSnS4 photovoltaic cells.” 2014. Doctoral Dissertation, Cranfield University. Accessed August 22, 2019. http://dspace.lib.cranfield.ac.uk/handle/1826/8771.

MLA Handbook (7th Edition):

Hutchings, K D. “High throughput combinatorial screening of Cu-Zn-Sn-S thin film libraries for the application of Cu2ZnSnS4 photovoltaic cells.” 2014. Web. 22 Aug 2019.

Vancouver:

Hutchings KD. High throughput combinatorial screening of Cu-Zn-Sn-S thin film libraries for the application of Cu2ZnSnS4 photovoltaic cells. [Internet] [Doctoral dissertation]. Cranfield University; 2014. [cited 2019 Aug 22]. Available from: http://dspace.lib.cranfield.ac.uk/handle/1826/8771.

Council of Science Editors:

Hutchings KD. High throughput combinatorial screening of Cu-Zn-Sn-S thin film libraries for the application of Cu2ZnSnS4 photovoltaic cells. [Doctoral Dissertation]. Cranfield University; 2014. Available from: http://dspace.lib.cranfield.ac.uk/handle/1826/8771


The Ohio State University

18. Trinh, Thi Ba. Synthesis and Screening of Peptide Libraries for Biological Applications.

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

Combinatorial chemistry is a powerful tool in medicinal chemistry as well as chemical biology. In this work, we have applied combinatorial chemistry toward the analysis… (more)

Subjects/Keywords: Chemistry; Combinatorial library, peptide cyclization, kinase profiling

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APA (6th Edition):

Trinh, T. B. (2014). Synthesis and Screening of Peptide Libraries for Biological Applications. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1405520102

Chicago Manual of Style (16th Edition):

Trinh, Thi Ba. “Synthesis and Screening of Peptide Libraries for Biological Applications.” 2014. Doctoral Dissertation, The Ohio State University. Accessed August 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1405520102.

MLA Handbook (7th Edition):

Trinh, Thi Ba. “Synthesis and Screening of Peptide Libraries for Biological Applications.” 2014. Web. 22 Aug 2019.

Vancouver:

Trinh TB. Synthesis and Screening of Peptide Libraries for Biological Applications. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2019 Aug 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1405520102.

Council of Science Editors:

Trinh TB. Synthesis and Screening of Peptide Libraries for Biological Applications. [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1405520102


Queensland University of Technology

19. Pow, Andrew James. Protein complementation assay as a display system for screening protein libraries in the intracellular environment.

Degree: 2008, Queensland University of Technology

 A wide range of screening strategies have been employed to isolate antibodies and other proteins with specific attributes, including binding affinity, specificity, stability and improved… (more)

Subjects/Keywords: protein complementation assay (PCA), â-lactamase, two-hybrid, molecular display, protein libraries, intracellular proteins, library screening, high-throughput screening, mammalian expression system, flow cytometry, single cell sorting, CCF2/AM; nitrocefin, HEK 293, HEK 293T, biopharmaceuticals

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APA (6th Edition):

Pow, A. J. (2008). Protein complementation assay as a display system for screening protein libraries in the intracellular environment. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/30392/

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):

Pow, Andrew James. “Protein complementation assay as a display system for screening protein libraries in the intracellular environment.” 2008. Thesis, Queensland University of Technology. Accessed August 22, 2019. https://eprints.qut.edu.au/30392/.

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

MLA Handbook (7th Edition):

Pow, Andrew James. “Protein complementation assay as a display system for screening protein libraries in the intracellular environment.” 2008. Web. 22 Aug 2019.

Vancouver:

Pow AJ. Protein complementation assay as a display system for screening protein libraries in the intracellular environment. [Internet] [Thesis]. Queensland University of Technology; 2008. [cited 2019 Aug 22]. Available from: https://eprints.qut.edu.au/30392/.

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

Council of Science Editors:

Pow AJ. Protein complementation assay as a display system for screening protein libraries in the intracellular environment. [Thesis]. Queensland University of Technology; 2008. Available from: https://eprints.qut.edu.au/30392/

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


Vanderbilt University

20. Fu, Darwin Yu. Improving Protein-Small Molecule Structure Predictions with Ensemble Methods, or Using Computers to Guess How Tiny Things Fit Together.

Degree: PhD, Chemistry, 2018, Vanderbilt University

Protein-small molecule structure prediction, or protein-ligand docking, is a computational method for modeling how binding partners will interaction on an atomic level. Accurate prediction of… (more)

Subjects/Keywords: Rosetta; Protein-Ligand Docking; Molecular Modeling; Small Molecules; G-Protein Coupled Receptors; Protein Structure Prediction

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APA (6th Edition):

Fu, D. Y. (2018). Improving Protein-Small Molecule Structure Predictions with Ensemble Methods, or Using Computers to Guess How Tiny Things Fit Together. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-08012018-164524/ ;

Chicago Manual of Style (16th Edition):

Fu, Darwin Yu. “Improving Protein-Small Molecule Structure Predictions with Ensemble Methods, or Using Computers to Guess How Tiny Things Fit Together.” 2018. Doctoral Dissertation, Vanderbilt University. Accessed August 22, 2019. http://etd.library.vanderbilt.edu/available/etd-08012018-164524/ ;.

MLA Handbook (7th Edition):

Fu, Darwin Yu. “Improving Protein-Small Molecule Structure Predictions with Ensemble Methods, or Using Computers to Guess How Tiny Things Fit Together.” 2018. Web. 22 Aug 2019.

Vancouver:

Fu DY. Improving Protein-Small Molecule Structure Predictions with Ensemble Methods, or Using Computers to Guess How Tiny Things Fit Together. [Internet] [Doctoral dissertation]. Vanderbilt University; 2018. [cited 2019 Aug 22]. Available from: http://etd.library.vanderbilt.edu/available/etd-08012018-164524/ ;.

Council of Science Editors:

Fu DY. Improving Protein-Small Molecule Structure Predictions with Ensemble Methods, or Using Computers to Guess How Tiny Things Fit Together. [Doctoral Dissertation]. Vanderbilt University; 2018. Available from: http://etd.library.vanderbilt.edu/available/etd-08012018-164524/ ;


University of Texas – Austin

21. Van Blarcom, Thomas John. Antibody discovery and engineering using the anchored periplasmic expression (APEx) Escherichia coli display system with flow cytometric selection.

Degree: Chemical Engineering, 2009, University of Texas – Austin

 The development of recombinant proteins for therapeutic applications has revolutionized the pharmaceutical industry. In particular, monoclonal antibodies are the safest class of all therapeutic molecules… (more)

Subjects/Keywords: Recombinant proteins; Monoclonal antibodies; Combinatorial library screening technologies; Anchored periplasmic expression; APEx; Escherichia Coli; High affinity antibodies

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APA (6th Edition):

Van Blarcom, T. J. (2009). Antibody discovery and engineering using the anchored periplasmic expression (APEx) Escherichia coli display system with flow cytometric selection. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/6903

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):

Van Blarcom, Thomas John. “Antibody discovery and engineering using the anchored periplasmic expression (APEx) Escherichia coli display system with flow cytometric selection.” 2009. Thesis, University of Texas – Austin. Accessed August 22, 2019. http://hdl.handle.net/2152/6903.

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

MLA Handbook (7th Edition):

Van Blarcom, Thomas John. “Antibody discovery and engineering using the anchored periplasmic expression (APEx) Escherichia coli display system with flow cytometric selection.” 2009. Web. 22 Aug 2019.

Vancouver:

Van Blarcom TJ. Antibody discovery and engineering using the anchored periplasmic expression (APEx) Escherichia coli display system with flow cytometric selection. [Internet] [Thesis]. University of Texas – Austin; 2009. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2152/6903.

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

Council of Science Editors:

Van Blarcom TJ. Antibody discovery and engineering using the anchored periplasmic expression (APEx) Escherichia coli display system with flow cytometric selection. [Thesis]. University of Texas – Austin; 2009. Available from: http://hdl.handle.net/2152/6903

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


Vanderbilt University

22. Combs, Steven Anthony. Identification and Scoring of Partial Covalent Interactions in Proteins and Protein Ligand Complexes.

Degree: PhD, Chemistry, 2013, Vanderbilt University

 Partial covalent interactions (PCI) such as hydrogen bonds, salt bridges, cation-π, and π-π interactions contribute to protein thermostability. Algorithms that identify PCIs rely on pairwise… (more)

Subjects/Keywords: protein modeling; ligand docking; rosetta; structural biology; computational chemistry

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APA (6th Edition):

Combs, S. A. (2013). Identification and Scoring of Partial Covalent Interactions in Proteins and Protein Ligand Complexes. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-12132013-151025/ ;

Chicago Manual of Style (16th Edition):

Combs, Steven Anthony. “Identification and Scoring of Partial Covalent Interactions in Proteins and Protein Ligand Complexes.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed August 22, 2019. http://etd.library.vanderbilt.edu/available/etd-12132013-151025/ ;.

MLA Handbook (7th Edition):

Combs, Steven Anthony. “Identification and Scoring of Partial Covalent Interactions in Proteins and Protein Ligand Complexes.” 2013. Web. 22 Aug 2019.

Vancouver:

Combs SA. Identification and Scoring of Partial Covalent Interactions in Proteins and Protein Ligand Complexes. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2019 Aug 22]. Available from: http://etd.library.vanderbilt.edu/available/etd-12132013-151025/ ;.

Council of Science Editors:

Combs SA. Identification and Scoring of Partial Covalent Interactions in Proteins and Protein Ligand Complexes. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://etd.library.vanderbilt.edu/available/etd-12132013-151025/ ;


University of North Texas

23. Brown, Jennifer Marie. Synthesis and Screening of a Combinatorial Peptide Library for Ligands to Target Transferrin: Miniaturizing the Library.

Degree: 2010, University of North Texas

Combinatorial libraries are used in the search for ligands that bind to target proteins. Fmoc solid-phase peptide synthesis is routinely used to generate such libraries.… (more)

Subjects/Keywords: Combinatorial; library; Peptides.; Ligands (Biochemistry); Transferrin.; Combinatorial chemistry.

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APA (6th Edition):

Brown, J. M. (2010). Synthesis and Screening of a Combinatorial Peptide Library for Ligands to Target Transferrin: Miniaturizing the Library. (Thesis). University of North Texas. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc30440/

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):

Brown, Jennifer Marie. “Synthesis and Screening of a Combinatorial Peptide Library for Ligands to Target Transferrin: Miniaturizing the Library.” 2010. Thesis, University of North Texas. Accessed August 22, 2019. https://digital.library.unt.edu/ark:/67531/metadc30440/.

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

MLA Handbook (7th Edition):

Brown, Jennifer Marie. “Synthesis and Screening of a Combinatorial Peptide Library for Ligands to Target Transferrin: Miniaturizing the Library.” 2010. Web. 22 Aug 2019.

Vancouver:

Brown JM. Synthesis and Screening of a Combinatorial Peptide Library for Ligands to Target Transferrin: Miniaturizing the Library. [Internet] [Thesis]. University of North Texas; 2010. [cited 2019 Aug 22]. Available from: https://digital.library.unt.edu/ark:/67531/metadc30440/.

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

Council of Science Editors:

Brown JM. Synthesis and Screening of a Combinatorial Peptide Library for Ligands to Target Transferrin: Miniaturizing the Library. [Thesis]. University of North Texas; 2010. Available from: https://digital.library.unt.edu/ark:/67531/metadc30440/

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


University of Kentucky

24. Sanchez Barrios, Andrea Marisa. BACTERIAL INOCULANTS, ENDOPHYTIC BACTERIA AND THEIR INFLUENCE ON NICOTIANA PHYSIOLOGY, DEVELOPMENT AND MICROBIOME.

Degree: 2018, University of Kentucky

 Soil and root microbial communities have been studied for decades, and the incorporation of high-throughput techniques and analysis has allowed the identification of endophytic/non-culturable organisms.… (more)

Subjects/Keywords: Nicotiana benthamiana; microbiome; core; inoculums; morphological traits; PAT-Seq; high-throughput; hormones; Agriculture; Computational Biology; Genetics and Genomics; Microbiology; Plant Biology

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APA (6th Edition):

Sanchez Barrios, A. M. (2018). BACTERIAL INOCULANTS, ENDOPHYTIC BACTERIA AND THEIR INFLUENCE ON NICOTIANA PHYSIOLOGY, DEVELOPMENT AND MICROBIOME. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pss_etds/101

Chicago Manual of Style (16th Edition):

Sanchez Barrios, Andrea Marisa. “BACTERIAL INOCULANTS, ENDOPHYTIC BACTERIA AND THEIR INFLUENCE ON NICOTIANA PHYSIOLOGY, DEVELOPMENT AND MICROBIOME.” 2018. Doctoral Dissertation, University of Kentucky. Accessed August 22, 2019. https://uknowledge.uky.edu/pss_etds/101.

MLA Handbook (7th Edition):

Sanchez Barrios, Andrea Marisa. “BACTERIAL INOCULANTS, ENDOPHYTIC BACTERIA AND THEIR INFLUENCE ON NICOTIANA PHYSIOLOGY, DEVELOPMENT AND MICROBIOME.” 2018. Web. 22 Aug 2019.

Vancouver:

Sanchez Barrios AM. BACTERIAL INOCULANTS, ENDOPHYTIC BACTERIA AND THEIR INFLUENCE ON NICOTIANA PHYSIOLOGY, DEVELOPMENT AND MICROBIOME. [Internet] [Doctoral dissertation]. University of Kentucky; 2018. [cited 2019 Aug 22]. Available from: https://uknowledge.uky.edu/pss_etds/101.

Council of Science Editors:

Sanchez Barrios AM. BACTERIAL INOCULANTS, ENDOPHYTIC BACTERIA AND THEIR INFLUENCE ON NICOTIANA PHYSIOLOGY, DEVELOPMENT AND MICROBIOME. [Doctoral Dissertation]. University of Kentucky; 2018. Available from: https://uknowledge.uky.edu/pss_etds/101


Vanderbilt University

25. DeLuca, Samuel Louis. Development of Novel Methods for Computational Protein Design and Protein-Ligand Docking.

Degree: PhD, Chemical and Physical Biology, 2015, Vanderbilt University

 The ability to make rapid predictions of macro-molecular structures will enable researchers to carry out effective protein design, virtual High Throughput Screening (vHTS) and rational… (more)

Subjects/Keywords: RosettaScripts; RosettaDesign; protein design; machine learning; Docking; Protein-Ligand Docking; Rosetta

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APA (6th Edition):

DeLuca, S. L. (2015). Development of Novel Methods for Computational Protein Design and Protein-Ligand Docking. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-07022015-151149/ ;

Chicago Manual of Style (16th Edition):

DeLuca, Samuel Louis. “Development of Novel Methods for Computational Protein Design and Protein-Ligand Docking.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed August 22, 2019. http://etd.library.vanderbilt.edu/available/etd-07022015-151149/ ;.

MLA Handbook (7th Edition):

DeLuca, Samuel Louis. “Development of Novel Methods for Computational Protein Design and Protein-Ligand Docking.” 2015. Web. 22 Aug 2019.

Vancouver:

DeLuca SL. Development of Novel Methods for Computational Protein Design and Protein-Ligand Docking. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2019 Aug 22]. Available from: http://etd.library.vanderbilt.edu/available/etd-07022015-151149/ ;.

Council of Science Editors:

DeLuca SL. Development of Novel Methods for Computational Protein Design and Protein-Ligand Docking. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://etd.library.vanderbilt.edu/available/etd-07022015-151149/ ;


University of Minnesota

26. Kurbanov, Elbek. Synthetic, Biochemical, X-ray Crystallographic, Computational and High-Throughput Screening Approaches Toward Anthrax Toxin Lethal Factor Inhibition.

Degree: PhD, Medicinal Chemistry, 2015, University of Minnesota

 The lethal factor (LF) enzyme secreted by Bacillus anthracis is chiefly responsible for anthrax-related cytotoxicity. In this dissertation, I present the computational design, synthesis, biochemical… (more)

Subjects/Keywords: anthrax; computational chemistry; high-throughput screening; lethal factor; structure-based inhibitor design; virtual screening

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APA (6th Edition):

Kurbanov, E. (2015). Synthetic, Biochemical, X-ray Crystallographic, Computational and High-Throughput Screening Approaches Toward Anthrax Toxin Lethal Factor Inhibition. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/192665

Chicago Manual of Style (16th Edition):

Kurbanov, Elbek. “Synthetic, Biochemical, X-ray Crystallographic, Computational and High-Throughput Screening Approaches Toward Anthrax Toxin Lethal Factor Inhibition.” 2015. Doctoral Dissertation, University of Minnesota. Accessed August 22, 2019. http://hdl.handle.net/11299/192665.

MLA Handbook (7th Edition):

Kurbanov, Elbek. “Synthetic, Biochemical, X-ray Crystallographic, Computational and High-Throughput Screening Approaches Toward Anthrax Toxin Lethal Factor Inhibition.” 2015. Web. 22 Aug 2019.

Vancouver:

Kurbanov E. Synthetic, Biochemical, X-ray Crystallographic, Computational and High-Throughput Screening Approaches Toward Anthrax Toxin Lethal Factor Inhibition. [Internet] [Doctoral dissertation]. University of Minnesota; 2015. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/11299/192665.

Council of Science Editors:

Kurbanov E. Synthetic, Biochemical, X-ray Crystallographic, Computational and High-Throughput Screening Approaches Toward Anthrax Toxin Lethal Factor Inhibition. [Doctoral Dissertation]. University of Minnesota; 2015. Available from: http://hdl.handle.net/11299/192665


University of Iowa

27. Mackie, Duncan Ian. High-throughput identification and characterization of novel inhibitors of Regulator of G Protein Signaling 17 as pretherapeutic leads for the treatment of lung and prostate cancers.

Degree: PhD, Pharmaceutical Sciences and Experimental Therapeutics, 2014, University of Iowa

  G–Protein Coupled Receptors are one of the most important targets in drug development, making up over 60% of drug targets. Recent studies have implicated… (more)

Subjects/Keywords: biochemical pharmacology; G protein coupled receptors; High-throughput screening; Lung and prostate cancers; RGS17; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Mackie, D. I. (2014). High-throughput identification and characterization of novel inhibitors of Regulator of G Protein Signaling 17 as pretherapeutic leads for the treatment of lung and prostate cancers. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/1986

Chicago Manual of Style (16th Edition):

Mackie, Duncan Ian. “High-throughput identification and characterization of novel inhibitors of Regulator of G Protein Signaling 17 as pretherapeutic leads for the treatment of lung and prostate cancers.” 2014. Doctoral Dissertation, University of Iowa. Accessed August 22, 2019. https://ir.uiowa.edu/etd/1986.

MLA Handbook (7th Edition):

Mackie, Duncan Ian. “High-throughput identification and characterization of novel inhibitors of Regulator of G Protein Signaling 17 as pretherapeutic leads for the treatment of lung and prostate cancers.” 2014. Web. 22 Aug 2019.

Vancouver:

Mackie DI. High-throughput identification and characterization of novel inhibitors of Regulator of G Protein Signaling 17 as pretherapeutic leads for the treatment of lung and prostate cancers. [Internet] [Doctoral dissertation]. University of Iowa; 2014. [cited 2019 Aug 22]. Available from: https://ir.uiowa.edu/etd/1986.

Council of Science Editors:

Mackie DI. High-throughput identification and characterization of novel inhibitors of Regulator of G Protein Signaling 17 as pretherapeutic leads for the treatment of lung and prostate cancers. [Doctoral Dissertation]. University of Iowa; 2014. Available from: https://ir.uiowa.edu/etd/1986


Delft University of Technology

28. Meijer, L.A. Bringing the Library home:.

Degree: 2010, Delft University of Technology

 With overloaded bookshelves, CD racks and film collections containing items that you do not necessarily need to keep, but neither want to throw away, we… (more)

Subjects/Keywords: design; library; interaction; product; service

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APA (6th Edition):

Meijer, L. A. (2010). Bringing the Library home:. (Masters Thesis). Delft University of Technology. Retrieved from http://resolver.tudelft.nl/uuid:3e257559-dcf7-428f-bda7-1b70d286ff9a

Chicago Manual of Style (16th Edition):

Meijer, L A. “Bringing the Library home:.” 2010. Masters Thesis, Delft University of Technology. Accessed August 22, 2019. http://resolver.tudelft.nl/uuid:3e257559-dcf7-428f-bda7-1b70d286ff9a.

MLA Handbook (7th Edition):

Meijer, L A. “Bringing the Library home:.” 2010. Web. 22 Aug 2019.

Vancouver:

Meijer LA. Bringing the Library home:. [Internet] [Masters thesis]. Delft University of Technology; 2010. [cited 2019 Aug 22]. Available from: http://resolver.tudelft.nl/uuid:3e257559-dcf7-428f-bda7-1b70d286ff9a.

Council of Science Editors:

Meijer LA. Bringing the Library home:. [Masters Thesis]. Delft University of Technology; 2010. Available from: http://resolver.tudelft.nl/uuid:3e257559-dcf7-428f-bda7-1b70d286ff9a


Delft University of Technology

29. Van Doorn, F. Challenging children to choose a book in the library:.

Degree: 2010, Delft University of Technology

 To become the most modern library of the world, DOK is developing new concepts to adapt to the needs of their visitors. The public library(more)

Subjects/Keywords: children; library; choices; design

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APA (6th Edition):

Van Doorn, F. (2010). Challenging children to choose a book in the library:. (Masters Thesis). Delft University of Technology. Retrieved from http://resolver.tudelft.nl/uuid:822781e0-a3cb-4345-95fe-bf08b333055d

Chicago Manual of Style (16th Edition):

Van Doorn, F. “Challenging children to choose a book in the library:.” 2010. Masters Thesis, Delft University of Technology. Accessed August 22, 2019. http://resolver.tudelft.nl/uuid:822781e0-a3cb-4345-95fe-bf08b333055d.

MLA Handbook (7th Edition):

Van Doorn, F. “Challenging children to choose a book in the library:.” 2010. Web. 22 Aug 2019.

Vancouver:

Van Doorn F. Challenging children to choose a book in the library:. [Internet] [Masters thesis]. Delft University of Technology; 2010. [cited 2019 Aug 22]. Available from: http://resolver.tudelft.nl/uuid:822781e0-a3cb-4345-95fe-bf08b333055d.

Council of Science Editors:

Van Doorn F. Challenging children to choose a book in the library:. [Masters Thesis]. Delft University of Technology; 2010. Available from: http://resolver.tudelft.nl/uuid:822781e0-a3cb-4345-95fe-bf08b333055d


University of Waikato

30. Feng, Chun. User preferences for the design of interfaces for library search pages .

Degree: 2017, University of Waikato

 As the digital revolution continues and the use of the Internet further develops, digital libraries have become an important tool for communication and development of… (more)

Subjects/Keywords: Library Search Interface Design

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

APA (6th Edition):

Feng, C. (2017). User preferences for the design of interfaces for library search pages . (Masters Thesis). University of Waikato. Retrieved from http://hdl.handle.net/10289/11573

Chicago Manual of Style (16th Edition):

Feng, Chun. “User preferences for the design of interfaces for library search pages .” 2017. Masters Thesis, University of Waikato. Accessed August 22, 2019. http://hdl.handle.net/10289/11573.

MLA Handbook (7th Edition):

Feng, Chun. “User preferences for the design of interfaces for library search pages .” 2017. Web. 22 Aug 2019.

Vancouver:

Feng C. User preferences for the design of interfaces for library search pages . [Internet] [Masters thesis]. University of Waikato; 2017. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/10289/11573.

Council of Science Editors:

Feng C. User preferences for the design of interfaces for library search pages . [Masters Thesis]. University of Waikato; 2017. Available from: http://hdl.handle.net/10289/11573

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