Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(Rop Rosetta protein G combinatorial library hydrophobic core library computational design high throughput). Showing records 1 – 30 of 122360 total matches.

[1] [2] [3] [4] [5] … [4079]

Search Limiters

Last 2 Years | English Only

Degrees

Levels

Languages

Country

▼ Search Limiters


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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. 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. 06 Aug 2020.

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 2020 Aug 06]. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. 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. 06 Aug 2020.

Vancouver:

Sen S. Engineering Proteins for Enhanced Stability using High-throughput and Combinatorial methods. [Internet] [Doctoral dissertation]. The Ohio State University; 2013. [cited 2020 Aug 06]. 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


Vanderbilt University

3. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. http://etd.library.vanderbilt.edu/available/etd-05182011-125917/ ;.

MLA Handbook (7th Edition):

Morin, Andrew. “The computational design of protein-ligand interfaces.” 2011. Web. 06 Aug 2020.

Vancouver:

Morin A. The computational design of protein-ligand interfaces. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2020 Aug 06]. 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

4. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. 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. 06 Aug 2020.

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 2020 Aug 06]. 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 Pennsylvania

5. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. 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. 06 Aug 2020.

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 2020 Aug 06]. 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


Cornell University

6. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. 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. 06 Aug 2020.

Vancouver:

Wong S. Probing the biophysical mechanisms of gene delivery by synthetic evolution of combinatorial polymeric vector libraries . [Internet] [Thesis]. Cornell University; 2008. [cited 2020 Aug 06]. 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


University of Minnesota

7. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. http://hdl.handle.net/11299/191350.

MLA Handbook (7th Edition):

Woldring, Daniel. “Constrained Diversification Enhances Protein Ligand Discovery and Evolution.” 2017. Web. 06 Aug 2020.

Vancouver:

Woldring D. Constrained Diversification Enhances Protein Ligand Discovery and Evolution. [Internet] [Doctoral dissertation]. University of Minnesota; 2017. [cited 2020 Aug 06]. 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 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. 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. 06 Aug 2020.

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 2020 Aug 06]. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. http://hdl.handle.net/1773/33593.

MLA Handbook (7th Edition):

Yu, Shawn. “Computational design of interleukin-2 mimetics.” 2015. Web. 06 Aug 2020.

Vancouver:

Yu S. Computational design of interleukin-2 mimetics. [Internet] [Doctoral dissertation]. University of Washington; 2015. [cited 2020 Aug 06]. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. 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. 06 Aug 2020.

Vancouver:

Haynes AR. Characterization of Extremophilic Bacteria for Potential in the Biofuel and Bioprocess Industries. [Internet] [Thesis]. Texas A&M University; 2014. [cited 2020 Aug 06]. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. 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. 06 Aug 2020.

Vancouver:

Allison BA. Computational Design of Protein-Ligand Interfaces Using RosettaLigand. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2020 Aug 06]. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. 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. 06 Aug 2020.

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 2020 Aug 06]. 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


University of Washington

13. Dang, Luke Thomas. Computational Design and Optimization of Novel Subtype Specific Frizzled Binding Proteins for Modulation of Wnt Signaling.

Degree: PhD, 2017, University of Washington

 Wnt signaling is essential to a range of critical biologic processes including embryonic development, mature tissue maintenance, and cell proliferation. Dysregulation of the Wnt signaling… (more)

Subjects/Keywords: Ankyrin Repeat Protein; Computational Protein Design; Frizzled; Protein Engineering; Rosetta; Wnt Signaling; Molecular biology; Biochemistry; Biomedical engineering; Molecular and cellular biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Dang, L. T. (2017). Computational Design and Optimization of Novel Subtype Specific Frizzled Binding Proteins for Modulation of Wnt Signaling. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/40260

Chicago Manual of Style (16th Edition):

Dang, Luke Thomas. “Computational Design and Optimization of Novel Subtype Specific Frizzled Binding Proteins for Modulation of Wnt Signaling.” 2017. Doctoral Dissertation, University of Washington. Accessed August 06, 2020. http://hdl.handle.net/1773/40260.

MLA Handbook (7th Edition):

Dang, Luke Thomas. “Computational Design and Optimization of Novel Subtype Specific Frizzled Binding Proteins for Modulation of Wnt Signaling.” 2017. Web. 06 Aug 2020.

Vancouver:

Dang LT. Computational Design and Optimization of Novel Subtype Specific Frizzled Binding Proteins for Modulation of Wnt Signaling. [Internet] [Doctoral dissertation]. University of Washington; 2017. [cited 2020 Aug 06]. Available from: http://hdl.handle.net/1773/40260.

Council of Science Editors:

Dang LT. Computational Design and Optimization of Novel Subtype Specific Frizzled Binding Proteins for Modulation of Wnt Signaling. [Doctoral Dissertation]. University of Washington; 2017. Available from: http://hdl.handle.net/1773/40260

14. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. 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. 06 Aug 2020.

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 2020 Aug 06]. 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

15. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. 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. 06 Aug 2020.

Vancouver:

Bender BJ. Knowledge-Based Modeling of G-Protein Coupled Receptors and their Binding Partners. [Internet] [Doctoral dissertation]. Vanderbilt University; 2019. [cited 2020 Aug 06]. 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

16. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. 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. 06 Aug 2020.

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 2020 Aug 06]. 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


The Ohio State University

17. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. 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. 06 Aug 2020.

Vancouver:

Trinh TB. Synthesis and Screening of Peptide Libraries for Biological Applications. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2020 Aug 06]. 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


Cranfield University

18. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. 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. 06 Aug 2020.

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 2020 Aug 06]. 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

19. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. 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. 06 Aug 2020.

Vancouver:

Hallen MA. Protein and Drug Design Algorithms Using Improved Biophysical Modeling . [Internet] [Thesis]. Duke University; 2016. [cited 2020 Aug 06]. 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


Queensland University of Technology

20. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. 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. 06 Aug 2020.

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 2020 Aug 06]. 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

21. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. 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. 06 Aug 2020.

Vancouver:

Combs SA. Identification and Scoring of Partial Covalent Interactions in Proteins and Protein Ligand Complexes. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2020 Aug 06]. 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/ ;


Vanderbilt University

22. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. 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. 06 Aug 2020.

Vancouver:

DeLuca SL. Development of Novel Methods for Computational Protein Design and Protein-Ligand Docking. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2020 Aug 06]. 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

23. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. 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. 06 Aug 2020.

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 2020 Aug 06]. 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

24. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 06, 2020. 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. 06 Aug 2020.

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 2020 Aug 06]. 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


University of Waikato

25. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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 06, 2020. 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. 06 Aug 2020.

Vancouver:

Feng C. User preferences for the design of interfaces for library search pages . [Internet] [Masters thesis]. University of Waikato; 2017. [cited 2020 Aug 06]. 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


University of Cambridge

26. Chong, Zheng Shan. Extracellular interaction screening using CRISPR activation.

Degree: PhD, 2019, University of Cambridge

 Extracellular interactions between cell surface receptors are necessary for signaling and adhesion but identifying them remains technically challenging. We describe a cell-based genome-wide approach employing… (more)

Subjects/Keywords: CRISPR; protein-protein interactions; high-throughput screening

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chong, Z. S. (2019). Extracellular interaction screening using CRISPR activation. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/291972 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774750

Chicago Manual of Style (16th Edition):

Chong, Zheng Shan. “Extracellular interaction screening using CRISPR activation.” 2019. Doctoral Dissertation, University of Cambridge. Accessed August 06, 2020. https://www.repository.cam.ac.uk/handle/1810/291972 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774750.

MLA Handbook (7th Edition):

Chong, Zheng Shan. “Extracellular interaction screening using CRISPR activation.” 2019. Web. 06 Aug 2020.

Vancouver:

Chong ZS. Extracellular interaction screening using CRISPR activation. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Aug 06]. Available from: https://www.repository.cam.ac.uk/handle/1810/291972 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774750.

Council of Science Editors:

Chong ZS. Extracellular interaction screening using CRISPR activation. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/291972 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774750


University of Washington

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

Degree: PhD, 2018, University of Washington

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

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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Frenz, Brandon Michael. “Advances In Computer Aided Protein Structure Determination From Sparse Cryo Electron Microscopy Data.” 2018. Doctoral Dissertation, University of Washington. Accessed August 06, 2020. http://hdl.handle.net/1773/40847.

MLA Handbook (7th Edition):

Frenz, Brandon Michael. “Advances In Computer Aided Protein Structure Determination From Sparse Cryo Electron Microscopy Data.” 2018. Web. 06 Aug 2020.

Vancouver:

Frenz BM. Advances In Computer Aided Protein Structure Determination From Sparse Cryo Electron Microscopy Data. [Internet] [Doctoral dissertation]. University of Washington; 2018. [cited 2020 Aug 06]. Available from: http://hdl.handle.net/1773/40847.

Council of Science Editors:

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


University of Washington

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

Degree: PhD, 2017, University of Washington

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

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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Lin, Yu-Ru. “Insight from designing ideal αβ monomers and homo-oligomers.” 2017. Doctoral Dissertation, University of Washington. Accessed August 06, 2020. http://hdl.handle.net/1773/39956.

MLA Handbook (7th Edition):

Lin, Yu-Ru. “Insight from designing ideal αβ monomers and homo-oligomers.” 2017. Web. 06 Aug 2020.

Vancouver:

Lin Y. Insight from designing ideal αβ monomers and homo-oligomers. [Internet] [Doctoral dissertation]. University of Washington; 2017. [cited 2020 Aug 06]. Available from: http://hdl.handle.net/1773/39956.

Council of Science Editors:

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


University of Washington

29. Clarke, Rachel. It's Not Rocket Library Science: Design Epistemology and American Librarianship.

Degree: PhD, 2016, University of Washington

 Contemporary American librarianship is typically considered a social science. Yet libraries and librarians have a strong history of making tools and services that enable access… (more)

Subjects/Keywords: design; epistemology; librarianship; library history; Library science; Design; information science

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Clarke, R. (2016). It's Not Rocket Library Science: Design Epistemology and American Librarianship. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/37159

Chicago Manual of Style (16th Edition):

Clarke, Rachel. “It's Not Rocket Library Science: Design Epistemology and American Librarianship.” 2016. Doctoral Dissertation, University of Washington. Accessed August 06, 2020. http://hdl.handle.net/1773/37159.

MLA Handbook (7th Edition):

Clarke, Rachel. “It's Not Rocket Library Science: Design Epistemology and American Librarianship.” 2016. Web. 06 Aug 2020.

Vancouver:

Clarke R. It's Not Rocket Library Science: Design Epistemology and American Librarianship. [Internet] [Doctoral dissertation]. University of Washington; 2016. [cited 2020 Aug 06]. Available from: http://hdl.handle.net/1773/37159.

Council of Science Editors:

Clarke R. It's Not Rocket Library Science: Design Epistemology and American Librarianship. [Doctoral Dissertation]. University of Washington; 2016. Available from: http://hdl.handle.net/1773/37159


Penn State University

30. Saraf, Manish Chandra. DEVELOPMENT OF COMPUTATIONAL TOOLS FOR THE DESIGN AND OPTIMIZATION OF COMBINATORIAL PROTEIN LIBRARIES.

Degree: PhD, Chemical Engineering, 2006, Penn State University

Combinatorial protein library generation and screening has emerged as a powerful strategy for protein engineering. In commonly used recombination protocols (e.g., DNA shuffling , StEP,… (more)

Subjects/Keywords: protein engineering; directed evolution; bioinformatics; protein library design; optimization

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Saraf, M. C. (2006). DEVELOPMENT OF COMPUTATIONAL TOOLS FOR THE DESIGN AND OPTIMIZATION OF COMBINATORIAL PROTEIN LIBRARIES. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/6934

Chicago Manual of Style (16th Edition):

Saraf, Manish Chandra. “DEVELOPMENT OF COMPUTATIONAL TOOLS FOR THE DESIGN AND OPTIMIZATION OF COMBINATORIAL PROTEIN LIBRARIES.” 2006. Doctoral Dissertation, Penn State University. Accessed August 06, 2020. https://etda.libraries.psu.edu/catalog/6934.

MLA Handbook (7th Edition):

Saraf, Manish Chandra. “DEVELOPMENT OF COMPUTATIONAL TOOLS FOR THE DESIGN AND OPTIMIZATION OF COMBINATORIAL PROTEIN LIBRARIES.” 2006. Web. 06 Aug 2020.

Vancouver:

Saraf MC. DEVELOPMENT OF COMPUTATIONAL TOOLS FOR THE DESIGN AND OPTIMIZATION OF COMBINATORIAL PROTEIN LIBRARIES. [Internet] [Doctoral dissertation]. Penn State University; 2006. [cited 2020 Aug 06]. Available from: https://etda.libraries.psu.edu/catalog/6934.

Council of Science Editors:

Saraf MC. DEVELOPMENT OF COMPUTATIONAL TOOLS FOR THE DESIGN AND OPTIMIZATION OF COMBINATORIAL PROTEIN LIBRARIES. [Doctoral Dissertation]. Penn State University; 2006. Available from: https://etda.libraries.psu.edu/catalog/6934

[1] [2] [3] [4] [5] … [4079]

.