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You searched for subject:(computational structural biology). Showing records 1 – 30 of 68 total matches.

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University of California – San Francisco

1. Greenberg, Charles Harold. Inferring Optimally Precise and Maximally Accurate Models from Electron Microscopy Data.

Degree: Biophysics, 2016, University of California – San Francisco

 Advances in electron microscopy (EM) allow for structure determination of large macromolecular machines at increasingly high resolutions. A key step in this process is interpreting… (more)

Subjects/Keywords: Biophysics; bayesian inference; computational biology; computational structure prediction; electron microscopy; molecular dynamics; structural biology

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APA (6th Edition):

Greenberg, C. H. (2016). Inferring Optimally Precise and Maximally Accurate Models from Electron Microscopy Data. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/9m1068f1

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):

Greenberg, Charles Harold. “Inferring Optimally Precise and Maximally Accurate Models from Electron Microscopy Data.” 2016. Thesis, University of California – San Francisco. Accessed August 12, 2020. http://www.escholarship.org/uc/item/9m1068f1.

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

MLA Handbook (7th Edition):

Greenberg, Charles Harold. “Inferring Optimally Precise and Maximally Accurate Models from Electron Microscopy Data.” 2016. Web. 12 Aug 2020.

Vancouver:

Greenberg CH. Inferring Optimally Precise and Maximally Accurate Models from Electron Microscopy Data. [Internet] [Thesis]. University of California – San Francisco; 2016. [cited 2020 Aug 12]. Available from: http://www.escholarship.org/uc/item/9m1068f1.

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

Council of Science Editors:

Greenberg CH. Inferring Optimally Precise and Maximally Accurate Models from Electron Microscopy Data. [Thesis]. University of California – San Francisco; 2016. Available from: http://www.escholarship.org/uc/item/9m1068f1

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


University of Oxford

2. Dunbar, James. Variable domain orientations in antigen receptors.

Degree: PhD, 2014, University of Oxford

 Specific recognition of pathogenic molecules by the immune system is mediated by proteins known as antigen receptors. One such component is the antibody. Binding properties… (more)

Subjects/Keywords: 616.07; Bioinformatics (life sciences); Computational biochemistry; Immunology; Antibodies; Structural Biology; Computational Biology; Protein Engineering

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APA (6th Edition):

Dunbar, J. (2014). Variable domain orientations in antigen receptors. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:30c18b4d-18a2-4f0d-895f-35cc24880955 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658505

Chicago Manual of Style (16th Edition):

Dunbar, James. “Variable domain orientations in antigen receptors.” 2014. Doctoral Dissertation, University of Oxford. Accessed August 12, 2020. http://ora.ox.ac.uk/objects/uuid:30c18b4d-18a2-4f0d-895f-35cc24880955 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658505.

MLA Handbook (7th Edition):

Dunbar, James. “Variable domain orientations in antigen receptors.” 2014. Web. 12 Aug 2020.

Vancouver:

Dunbar J. Variable domain orientations in antigen receptors. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2020 Aug 12]. Available from: http://ora.ox.ac.uk/objects/uuid:30c18b4d-18a2-4f0d-895f-35cc24880955 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658505.

Council of Science Editors:

Dunbar J. Variable domain orientations in antigen receptors. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:30c18b4d-18a2-4f0d-895f-35cc24880955 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658505


Western Kentucky University

3. Katare, Nitin Tanajirao. Synthesis and Molecular Mechanics Study of Platinum Triamine Complex with N-Acetyl-L-Methionine and Guanosine 5’monophosphate.

Degree: MS, Department of Chemistry, 2020, Western Kentucky University

  Cisplatin and its analogues have been used and tested over decades for cancer treatment, but because of the serious side effects, it is important… (more)

Subjects/Keywords: Platinum complex; anticancer drug; computational chemistry; Biochemistry, Biophysics, and Structural Biology; Chemistry; Computational Biology

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APA (6th Edition):

Katare, N. T. (2020). Synthesis and Molecular Mechanics Study of Platinum Triamine Complex with N-Acetyl-L-Methionine and Guanosine 5’monophosphate. (Masters Thesis). Western Kentucky University. Retrieved from https://digitalcommons.wku.edu/theses/3200

Chicago Manual of Style (16th Edition):

Katare, Nitin Tanajirao. “Synthesis and Molecular Mechanics Study of Platinum Triamine Complex with N-Acetyl-L-Methionine and Guanosine 5’monophosphate.” 2020. Masters Thesis, Western Kentucky University. Accessed August 12, 2020. https://digitalcommons.wku.edu/theses/3200.

MLA Handbook (7th Edition):

Katare, Nitin Tanajirao. “Synthesis and Molecular Mechanics Study of Platinum Triamine Complex with N-Acetyl-L-Methionine and Guanosine 5’monophosphate.” 2020. Web. 12 Aug 2020.

Vancouver:

Katare NT. Synthesis and Molecular Mechanics Study of Platinum Triamine Complex with N-Acetyl-L-Methionine and Guanosine 5’monophosphate. [Internet] [Masters thesis]. Western Kentucky University; 2020. [cited 2020 Aug 12]. Available from: https://digitalcommons.wku.edu/theses/3200.

Council of Science Editors:

Katare NT. Synthesis and Molecular Mechanics Study of Platinum Triamine Complex with N-Acetyl-L-Methionine and Guanosine 5’monophosphate. [Masters Thesis]. Western Kentucky University; 2020. Available from: https://digitalcommons.wku.edu/theses/3200


University of Rochester

4. Sloma, Michael F. Computational Tools for RNA Structure Prediction.

Degree: PhD, 2018, University of Rochester

 RNA is a versatile biomolecule that functions in many cellular processes. In addition to acting as a template for protein synthesis, RNA plays a direct… (more)

Subjects/Keywords: RNA; Secondary structure; Structure prediction; Bioinformatics; Computational biology; Structural biology.

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APA (6th Edition):

Sloma, M. F. (2018). Computational Tools for RNA Structure Prediction. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/33903

Chicago Manual of Style (16th Edition):

Sloma, Michael F. “Computational Tools for RNA Structure Prediction.” 2018. Doctoral Dissertation, University of Rochester. Accessed August 12, 2020. http://hdl.handle.net/1802/33903.

MLA Handbook (7th Edition):

Sloma, Michael F. “Computational Tools for RNA Structure Prediction.” 2018. Web. 12 Aug 2020.

Vancouver:

Sloma MF. Computational Tools for RNA Structure Prediction. [Internet] [Doctoral dissertation]. University of Rochester; 2018. [cited 2020 Aug 12]. Available from: http://hdl.handle.net/1802/33903.

Council of Science Editors:

Sloma MF. Computational Tools for RNA Structure Prediction. [Doctoral Dissertation]. University of Rochester; 2018. Available from: http://hdl.handle.net/1802/33903


University of Washington

5. Chen, Zibo. Programmable Design of Protein Interaction Specificity and Logic Gates.

Degree: PhD, 2019, University of Washington

 The binding specificity of DNA molecules is straightforward: adenine binds thymine, and cytosine binds guanine. This simple encoding of specificity enables the binding between two… (more)

Subjects/Keywords: Biophysics; Computational biology; Structural biology; Biochemistry; Biological chemistry

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APA (6th Edition):

Chen, Z. (2019). Programmable Design of Protein Interaction Specificity and Logic Gates. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/43306

Chicago Manual of Style (16th Edition):

Chen, Zibo. “Programmable Design of Protein Interaction Specificity and Logic Gates.” 2019. Doctoral Dissertation, University of Washington. Accessed August 12, 2020. http://hdl.handle.net/1773/43306.

MLA Handbook (7th Edition):

Chen, Zibo. “Programmable Design of Protein Interaction Specificity and Logic Gates.” 2019. Web. 12 Aug 2020.

Vancouver:

Chen Z. Programmable Design of Protein Interaction Specificity and Logic Gates. [Internet] [Doctoral dissertation]. University of Washington; 2019. [cited 2020 Aug 12]. Available from: http://hdl.handle.net/1773/43306.

Council of Science Editors:

Chen Z. Programmable Design of Protein Interaction Specificity and Logic Gates. [Doctoral Dissertation]. University of Washington; 2019. Available from: http://hdl.handle.net/1773/43306

6. Nobrega, Robert P. Early Folding Biases in the Folding Free-Energy Surface of βα-Repeat Proteins: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2014, U of Massachusetts : Med

  Early events in folding can determine if a protein is going to fold, misfold, or aggregate. Understanding these deterministic events is paramount for de… (more)

Subjects/Keywords: Protein Folding; Protein Engineering; Proteins; Biochemistry; Biophysics; Computational Biology; Molecular Biology; Structural Biology

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APA (6th Edition):

Nobrega, R. P. (2014). Early Folding Biases in the Folding Free-Energy Surface of βα-Repeat Proteins: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/723

Chicago Manual of Style (16th Edition):

Nobrega, Robert P. “Early Folding Biases in the Folding Free-Energy Surface of βα-Repeat Proteins: A Dissertation.” 2014. Doctoral Dissertation, U of Massachusetts : Med. Accessed August 12, 2020. http://escholarship.umassmed.edu/gsbs_diss/723.

MLA Handbook (7th Edition):

Nobrega, Robert P. “Early Folding Biases in the Folding Free-Energy Surface of βα-Repeat Proteins: A Dissertation.” 2014. Web. 12 Aug 2020.

Vancouver:

Nobrega RP. Early Folding Biases in the Folding Free-Energy Surface of βα-Repeat Proteins: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2014. [cited 2020 Aug 12]. Available from: http://escholarship.umassmed.edu/gsbs_diss/723.

Council of Science Editors:

Nobrega RP. Early Folding Biases in the Folding Free-Energy Surface of βα-Repeat Proteins: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2014. Available from: http://escholarship.umassmed.edu/gsbs_diss/723


King Abdullah University of Science and Technology

7. Guzmán-Vega, Francisco J. Applications in computational structural biology: the generation of a protein modelling pipeline and the structural analysis of patient-derived mutations.

Degree: 2019, King Abdullah University of Science and Technology

 Besides helping us advance the understanding of the physicochemical principles governing the three-dimensional folding of proteins and their mechanisms of action, the ability to build,… (more)

Subjects/Keywords: Computational Biology; Structural Biology; Synthetic Biology; Protein Structure; Mutation Effect Prediction; Human Disease

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APA (6th Edition):

Guzmán-Vega, F. J. (2019). Applications in computational structural biology: the generation of a protein modelling pipeline and the structural analysis of patient-derived mutations. (Thesis). King Abdullah University of Science and Technology. Retrieved from http://hdl.handle.net/10754/652872

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):

Guzmán-Vega, Francisco J. “Applications in computational structural biology: the generation of a protein modelling pipeline and the structural analysis of patient-derived mutations.” 2019. Thesis, King Abdullah University of Science and Technology. Accessed August 12, 2020. http://hdl.handle.net/10754/652872.

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

MLA Handbook (7th Edition):

Guzmán-Vega, Francisco J. “Applications in computational structural biology: the generation of a protein modelling pipeline and the structural analysis of patient-derived mutations.” 2019. Web. 12 Aug 2020.

Vancouver:

Guzmán-Vega FJ. Applications in computational structural biology: the generation of a protein modelling pipeline and the structural analysis of patient-derived mutations. [Internet] [Thesis]. King Abdullah University of Science and Technology; 2019. [cited 2020 Aug 12]. Available from: http://hdl.handle.net/10754/652872.

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

Council of Science Editors:

Guzmán-Vega FJ. Applications in computational structural biology: the generation of a protein modelling pipeline and the structural analysis of patient-derived mutations. [Thesis]. King Abdullah University of Science and Technology; 2019. Available from: http://hdl.handle.net/10754/652872

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


INP Toulouse

8. Denarie, Laurent. Robotics-inspired methods to enhance protein design : Méthodes inspirées de la robotique pour l’aide à la conception de protéines.

Degree: Docteur es, Intelligence Artificielle, 2017, INP Toulouse

La conception de protéines ayant des propriétés spécifiques représente un enjeu majeur pour la pharmacologie et les bio-technologies. Malgré les progrès des méthodes de CAO… (more)

Subjects/Keywords: Planification de mouvement; Conception de protéines; Biologie structurelle; Robotique; Bioinformatique; Path planning; Protein design; Structural biology; Robotics; Sampling-based algorithms; Computational biology

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APA (6th Edition):

Denarie, L. (2017). Robotics-inspired methods to enhance protein design : Méthodes inspirées de la robotique pour l’aide à la conception de protéines. (Doctoral Dissertation). INP Toulouse. Retrieved from http://www.theses.fr/2017INPT0029

Chicago Manual of Style (16th Edition):

Denarie, Laurent. “Robotics-inspired methods to enhance protein design : Méthodes inspirées de la robotique pour l’aide à la conception de protéines.” 2017. Doctoral Dissertation, INP Toulouse. Accessed August 12, 2020. http://www.theses.fr/2017INPT0029.

MLA Handbook (7th Edition):

Denarie, Laurent. “Robotics-inspired methods to enhance protein design : Méthodes inspirées de la robotique pour l’aide à la conception de protéines.” 2017. Web. 12 Aug 2020.

Vancouver:

Denarie L. Robotics-inspired methods to enhance protein design : Méthodes inspirées de la robotique pour l’aide à la conception de protéines. [Internet] [Doctoral dissertation]. INP Toulouse; 2017. [cited 2020 Aug 12]. Available from: http://www.theses.fr/2017INPT0029.

Council of Science Editors:

Denarie L. Robotics-inspired methods to enhance protein design : Méthodes inspirées de la robotique pour l’aide à la conception de protéines. [Doctoral Dissertation]. INP Toulouse; 2017. Available from: http://www.theses.fr/2017INPT0029


Vanderbilt University

9. Nguyen, Elizabeth Dong. Structural Studies of the Interaction between mGlu5 and Allosteric Modulators.

Degree: PhD, Chemical and Physical Biology, 2013, Vanderbilt University

 The metabotropic glutamate receptor subtype 5 (mGlu5), a class C G-protein coupled receptor (GPCR), is involved in cognitive function through diverse signaling pathways that modulate… (more)

Subjects/Keywords: ligand docking; GPCR; schizophrenia; computational structural biology; protein structure prediction

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APA (6th Edition):

Nguyen, E. D. (2013). Structural Studies of the Interaction between mGlu5 and Allosteric Modulators. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-07172013-164828/ ;

Chicago Manual of Style (16th Edition):

Nguyen, Elizabeth Dong. “Structural Studies of the Interaction between mGlu5 and Allosteric Modulators.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed August 12, 2020. http://etd.library.vanderbilt.edu/available/etd-07172013-164828/ ;.

MLA Handbook (7th Edition):

Nguyen, Elizabeth Dong. “Structural Studies of the Interaction between mGlu5 and Allosteric Modulators.” 2013. Web. 12 Aug 2020.

Vancouver:

Nguyen ED. Structural Studies of the Interaction between mGlu5 and Allosteric Modulators. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2020 Aug 12]. Available from: http://etd.library.vanderbilt.edu/available/etd-07172013-164828/ ;.

Council of Science Editors:

Nguyen ED. Structural Studies of the Interaction between mGlu5 and Allosteric Modulators. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://etd.library.vanderbilt.edu/available/etd-07172013-164828/ ;


Vanderbilt University

10. 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 12, 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. 12 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 12]. 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 Toronto

11. Sun, Mark George Ford. Strategies for Protein Engineering.

Degree: PhD, 2016, University of Toronto

 Proteins propagate information within a cell by interacting with other proteins, DNA, RNA, and small molecules, enabling a cell to adapt to its environment and… (more)

Subjects/Keywords: Computational Protein Design; Protein Engineering; Structural Biology; 0715

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APA (6th Edition):

Sun, M. G. F. (2016). Strategies for Protein Engineering. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/77408

Chicago Manual of Style (16th Edition):

Sun, Mark George Ford. “Strategies for Protein Engineering.” 2016. Doctoral Dissertation, University of Toronto. Accessed August 12, 2020. http://hdl.handle.net/1807/77408.

MLA Handbook (7th Edition):

Sun, Mark George Ford. “Strategies for Protein Engineering.” 2016. Web. 12 Aug 2020.

Vancouver:

Sun MGF. Strategies for Protein Engineering. [Internet] [Doctoral dissertation]. University of Toronto; 2016. [cited 2020 Aug 12]. Available from: http://hdl.handle.net/1807/77408.

Council of Science Editors:

Sun MGF. Strategies for Protein Engineering. [Doctoral Dissertation]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/77408


University of Hong Kong

12. Peng, Zeshan. Structure comparison in bioinformatics.

Degree: 2006, University of Hong Kong

Subjects/Keywords: Computational biology.; Structural bioinformatics.

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APA (6th Edition):

Peng, Z. (2006). Structure comparison in bioinformatics. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/41351

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):

Peng, Zeshan. “Structure comparison in bioinformatics.” 2006. Thesis, University of Hong Kong. Accessed August 12, 2020. http://hdl.handle.net/10722/41351.

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

MLA Handbook (7th Edition):

Peng, Zeshan. “Structure comparison in bioinformatics.” 2006. Web. 12 Aug 2020.

Vancouver:

Peng Z. Structure comparison in bioinformatics. [Internet] [Thesis]. University of Hong Kong; 2006. [cited 2020 Aug 12]. Available from: http://hdl.handle.net/10722/41351.

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

Council of Science Editors:

Peng Z. Structure comparison in bioinformatics. [Thesis]. University of Hong Kong; 2006. Available from: http://hdl.handle.net/10722/41351

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


University of New Mexico

13. Manavi, Kasra. Multi-Resolution Analysis of Large Molecular Structures and Interactions.

Degree: Department of Computer Science, 2018, University of New Mexico

  Simulation of large molecular structures and their interactions has become a major component of modern biomolecular research. Methods to simulate these type of molecules… (more)

Subjects/Keywords: Coarse Grained Modeling; Computational Biology; Structural Biology; Cryo EM; Artificial Intelligence and Robotics; Bioinformatics; Numerical Analysis and Scientific Computing; Structural Biology

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APA (6th Edition):

Manavi, K. (2018). Multi-Resolution Analysis of Large Molecular Structures and Interactions. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/cs_etds/94

Chicago Manual of Style (16th Edition):

Manavi, Kasra. “Multi-Resolution Analysis of Large Molecular Structures and Interactions.” 2018. Doctoral Dissertation, University of New Mexico. Accessed August 12, 2020. https://digitalrepository.unm.edu/cs_etds/94.

MLA Handbook (7th Edition):

Manavi, Kasra. “Multi-Resolution Analysis of Large Molecular Structures and Interactions.” 2018. Web. 12 Aug 2020.

Vancouver:

Manavi K. Multi-Resolution Analysis of Large Molecular Structures and Interactions. [Internet] [Doctoral dissertation]. University of New Mexico; 2018. [cited 2020 Aug 12]. Available from: https://digitalrepository.unm.edu/cs_etds/94.

Council of Science Editors:

Manavi K. Multi-Resolution Analysis of Large Molecular Structures and Interactions. [Doctoral Dissertation]. University of New Mexico; 2018. Available from: https://digitalrepository.unm.edu/cs_etds/94

14. Oliveira, Saulo Henrique Pires de. Desenvolvimento de um algoritmo para identificação e caracterização de cavidades em regiões específicas de estruturas tridimensionais de proteínas.

Degree: Mestrado, Bioinformática, 2011, University of São Paulo

A identificação e caracterização geométrica e físico-química de espaços vazios na estrutura tridimensional de proteínas é capaz de agregar informações importantes para guiar o desenho… (more)

Subjects/Keywords: bioinformática; Bioinformatics; biologia computacional; biologia estrutural; Cavidades proteicas; Computational Biology; Protein Cavities; Structural Biology

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APA (6th Edition):

Oliveira, S. H. P. d. (2011). Desenvolvimento de um algoritmo para identificação e caracterização de cavidades em regiões específicas de estruturas tridimensionais de proteínas. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/95/95131/tde-14072011-052430/ ;

Chicago Manual of Style (16th Edition):

Oliveira, Saulo Henrique Pires de. “Desenvolvimento de um algoritmo para identificação e caracterização de cavidades em regiões específicas de estruturas tridimensionais de proteínas.” 2011. Masters Thesis, University of São Paulo. Accessed August 12, 2020. http://www.teses.usp.br/teses/disponiveis/95/95131/tde-14072011-052430/ ;.

MLA Handbook (7th Edition):

Oliveira, Saulo Henrique Pires de. “Desenvolvimento de um algoritmo para identificação e caracterização de cavidades em regiões específicas de estruturas tridimensionais de proteínas.” 2011. Web. 12 Aug 2020.

Vancouver:

Oliveira SHPd. Desenvolvimento de um algoritmo para identificação e caracterização de cavidades em regiões específicas de estruturas tridimensionais de proteínas. [Internet] [Masters thesis]. University of São Paulo; 2011. [cited 2020 Aug 12]. Available from: http://www.teses.usp.br/teses/disponiveis/95/95131/tde-14072011-052430/ ;.

Council of Science Editors:

Oliveira SHPd. Desenvolvimento de um algoritmo para identificação e caracterização de cavidades em regiões específicas de estruturas tridimensionais de proteínas. [Masters Thesis]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/95/95131/tde-14072011-052430/ ;


University of Pennsylvania

15. Petty II, Thomas John. Probabilistic Protein Design, Comparative Modeling, and the Structure of a Multidomain P53 Oligomer Bound to DNA.

Degree: 2010, University of Pennsylvania

 Proteins are the main functional components of all cellular processes, and most of them fold into unique three-dimensional shapes guided by their amino-acid sequence. Discovering… (more)

Subjects/Keywords: Comparative Modeling; Protein Design; p53; DNA binding; Multi-domain; Microfluidics; Biochemistry; Computational Biology; Structural Biology

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APA (6th Edition):

Petty II, T. J. (2010). Probabilistic Protein Design, Comparative Modeling, and the Structure of a Multidomain P53 Oligomer Bound to DNA. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/412

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):

Petty II, Thomas John. “Probabilistic Protein Design, Comparative Modeling, and the Structure of a Multidomain P53 Oligomer Bound to DNA.” 2010. Thesis, University of Pennsylvania. Accessed August 12, 2020. https://repository.upenn.edu/edissertations/412.

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

MLA Handbook (7th Edition):

Petty II, Thomas John. “Probabilistic Protein Design, Comparative Modeling, and the Structure of a Multidomain P53 Oligomer Bound to DNA.” 2010. Web. 12 Aug 2020.

Vancouver:

Petty II TJ. Probabilistic Protein Design, Comparative Modeling, and the Structure of a Multidomain P53 Oligomer Bound to DNA. [Internet] [Thesis]. University of Pennsylvania; 2010. [cited 2020 Aug 12]. Available from: https://repository.upenn.edu/edissertations/412.

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

Council of Science Editors:

Petty II TJ. Probabilistic Protein Design, Comparative Modeling, and the Structure of a Multidomain P53 Oligomer Bound to DNA. [Thesis]. University of Pennsylvania; 2010. Available from: https://repository.upenn.edu/edissertations/412

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


University of Pennsylvania

16. Coleman, Ryan G. Shortest Geometric Paths Analysis in Structural Biology.

Degree: 2009, University of Pennsylvania

 The surface of a macromolecule, such as a protein, represents the contact point of any interaction that molecule has with solvent, ions, small molecules or… (more)

Subjects/Keywords: protein pockets depth holes shape geometry; Computational Biology; Structural Biology; Theory and Algorithms

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APA (6th Edition):

Coleman, R. G. (2009). Shortest Geometric Paths Analysis in Structural Biology. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/31

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):

Coleman, Ryan G. “Shortest Geometric Paths Analysis in Structural Biology.” 2009. Thesis, University of Pennsylvania. Accessed August 12, 2020. https://repository.upenn.edu/edissertations/31.

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

MLA Handbook (7th Edition):

Coleman, Ryan G. “Shortest Geometric Paths Analysis in Structural Biology.” 2009. Web. 12 Aug 2020.

Vancouver:

Coleman RG. Shortest Geometric Paths Analysis in Structural Biology. [Internet] [Thesis]. University of Pennsylvania; 2009. [cited 2020 Aug 12]. Available from: https://repository.upenn.edu/edissertations/31.

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

Council of Science Editors:

Coleman RG. Shortest Geometric Paths Analysis in Structural Biology. [Thesis]. University of Pennsylvania; 2009. Available from: https://repository.upenn.edu/edissertations/31

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


East Tennessee State University

17. Griffin, Jeddidiah. Quantitative Studies of Amyloidogenic Protein Residue Interaction Networks and Abnormal Ammonia Metabolism in Neurotoxicity and Disease.

Degree: PhD, Biomedical Sciences, 2018, East Tennessee State University

  Investigating similarities among neurological diseases can provide insight into disease processes. Two prominent commonalities of neurological diseases are the formation of amyloid deposits and… (more)

Subjects/Keywords: Ammonia; Glutamate; Alzheimer’s Disease; Amyloid; Residue Interaction Network; Biochemistry; Computational Biology; Structural Biology

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APA (6th Edition):

Griffin, J. (2018). Quantitative Studies of Amyloidogenic Protein Residue Interaction Networks and Abnormal Ammonia Metabolism in Neurotoxicity and Disease. (Doctoral Dissertation). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/3451

Chicago Manual of Style (16th Edition):

Griffin, Jeddidiah. “Quantitative Studies of Amyloidogenic Protein Residue Interaction Networks and Abnormal Ammonia Metabolism in Neurotoxicity and Disease.” 2018. Doctoral Dissertation, East Tennessee State University. Accessed August 12, 2020. https://dc.etsu.edu/etd/3451.

MLA Handbook (7th Edition):

Griffin, Jeddidiah. “Quantitative Studies of Amyloidogenic Protein Residue Interaction Networks and Abnormal Ammonia Metabolism in Neurotoxicity and Disease.” 2018. Web. 12 Aug 2020.

Vancouver:

Griffin J. Quantitative Studies of Amyloidogenic Protein Residue Interaction Networks and Abnormal Ammonia Metabolism in Neurotoxicity and Disease. [Internet] [Doctoral dissertation]. East Tennessee State University; 2018. [cited 2020 Aug 12]. Available from: https://dc.etsu.edu/etd/3451.

Council of Science Editors:

Griffin J. Quantitative Studies of Amyloidogenic Protein Residue Interaction Networks and Abnormal Ammonia Metabolism in Neurotoxicity and Disease. [Doctoral Dissertation]. East Tennessee State University; 2018. Available from: https://dc.etsu.edu/etd/3451


University of Oxford

18. Busch, Julia Maria Christiane. The making and breaking of SAS-6 : structural insights and inhibitor search for n-terminal domain dimerisation.

Degree: PhD, 2017, University of Oxford

 SAS-6 is the structural core of the forming centriole - a cylindrical protein complex, which is an essential component of the centrosome. Oligomerisation of SAS-6… (more)

Subjects/Keywords: 572; Structural Biology; Computational biology; Biochemistry; Biophysics; Protein Dimerisation; Centriole; SAS-6; Inhibitor Screening; STIL

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APA (6th Edition):

Busch, J. M. C. (2017). The making and breaking of SAS-6 : structural insights and inhibitor search for n-terminal domain dimerisation. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:2d5e4713-e645-40e9-87a1-88a7425d93eb ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.757699

Chicago Manual of Style (16th Edition):

Busch, Julia Maria Christiane. “The making and breaking of SAS-6 : structural insights and inhibitor search for n-terminal domain dimerisation.” 2017. Doctoral Dissertation, University of Oxford. Accessed August 12, 2020. http://ora.ox.ac.uk/objects/uuid:2d5e4713-e645-40e9-87a1-88a7425d93eb ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.757699.

MLA Handbook (7th Edition):

Busch, Julia Maria Christiane. “The making and breaking of SAS-6 : structural insights and inhibitor search for n-terminal domain dimerisation.” 2017. Web. 12 Aug 2020.

Vancouver:

Busch JMC. The making and breaking of SAS-6 : structural insights and inhibitor search for n-terminal domain dimerisation. [Internet] [Doctoral dissertation]. University of Oxford; 2017. [cited 2020 Aug 12]. Available from: http://ora.ox.ac.uk/objects/uuid:2d5e4713-e645-40e9-87a1-88a7425d93eb ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.757699.

Council of Science Editors:

Busch JMC. The making and breaking of SAS-6 : structural insights and inhibitor search for n-terminal domain dimerisation. [Doctoral Dissertation]. University of Oxford; 2017. Available from: http://ora.ox.ac.uk/objects/uuid:2d5e4713-e645-40e9-87a1-88a7425d93eb ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.757699


Georgia Tech

19. Rogers, Emily. A novel method for cluster analysis of RNA structural data.

Degree: PhD, Computational Science and Engineering, 2018, Georgia Tech

 Functional RNA is known to contribute to a host of important biological pathways, with new discoveries being made daily. Because function is dependent on structure,… (more)

Subjects/Keywords: Computational biology; Structural biology; RNA folding; Boltzmann sampling; Cluster analysis; RNA secondary structure prediction

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

APA (6th Edition):

Rogers, E. (2018). A novel method for cluster analysis of RNA structural data. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60232

Chicago Manual of Style (16th Edition):

Rogers, Emily. “A novel method for cluster analysis of RNA structural data.” 2018. Doctoral Dissertation, Georgia Tech. Accessed August 12, 2020. http://hdl.handle.net/1853/60232.

MLA Handbook (7th Edition):

Rogers, Emily. “A novel method for cluster analysis of RNA structural data.” 2018. Web. 12 Aug 2020.

Vancouver:

Rogers E. A novel method for cluster analysis of RNA structural data. [Internet] [Doctoral dissertation]. Georgia Tech; 2018. [cited 2020 Aug 12]. Available from: http://hdl.handle.net/1853/60232.

Council of Science Editors:

Rogers E. A novel method for cluster analysis of RNA structural data. [Doctoral Dissertation]. Georgia Tech; 2018. Available from: http://hdl.handle.net/1853/60232


Vanderbilt University

20. Teixeira, Pedro Luis, Jr. Using Evolutionarily-Based Correlation Measures and Machine Learning to Improve Protein Structure Prediction in BCL::Fold.

Degree: MS, Biomedical Informatics, 2014, Vanderbilt University

 De novo protein structure prediction is a challenge due to the sheer size of the search space. One can limit the set of potential models… (more)

Subjects/Keywords: direct information; artificial neural networks; computational structural biology; correlation; protein folding; computational biology; machine learning; decision trees

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APA (6th Edition):

Teixeira, Pedro Luis, J. (2014). Using Evolutionarily-Based Correlation Measures and Machine Learning to Improve Protein Structure Prediction in BCL::Fold. (Masters Thesis). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-06062014-110802/ ;

Chicago Manual of Style (16th Edition):

Teixeira, Pedro Luis, Jr. “Using Evolutionarily-Based Correlation Measures and Machine Learning to Improve Protein Structure Prediction in BCL::Fold.” 2014. Masters Thesis, Vanderbilt University. Accessed August 12, 2020. http://etd.library.vanderbilt.edu/available/etd-06062014-110802/ ;.

MLA Handbook (7th Edition):

Teixeira, Pedro Luis, Jr. “Using Evolutionarily-Based Correlation Measures and Machine Learning to Improve Protein Structure Prediction in BCL::Fold.” 2014. Web. 12 Aug 2020.

Vancouver:

Teixeira, Pedro Luis J. Using Evolutionarily-Based Correlation Measures and Machine Learning to Improve Protein Structure Prediction in BCL::Fold. [Internet] [Masters thesis]. Vanderbilt University; 2014. [cited 2020 Aug 12]. Available from: http://etd.library.vanderbilt.edu/available/etd-06062014-110802/ ;.

Council of Science Editors:

Teixeira, Pedro Luis J. Using Evolutionarily-Based Correlation Measures and Machine Learning to Improve Protein Structure Prediction in BCL::Fold. [Masters Thesis]. Vanderbilt University; 2014. Available from: http://etd.library.vanderbilt.edu/available/etd-06062014-110802/ ;

21. Zhuang, Jiali. Structural Variation Discovery and Genotyping from Whole Genome Sequencing: Methodology and Applications: A Dissertation.

Degree: Bioinformatics and Computational Biology, Biochemistry and Molecular Pharmacology, 2015, U of Massachusetts : Med

  A comprehensive understanding about how genetic variants and mutations contribute to phenotypic variations and alterations entails experimental technologies and analytical methodologies that are able… (more)

Subjects/Keywords: Genomic Structural Variation; DNA Transposable Elements; Genome-Wide Association Study; Bioinformatics; Computational Biology; Genomics

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

APA (6th Edition):

Zhuang, J. (2015). Structural Variation Discovery and Genotyping from Whole Genome Sequencing: Methodology and Applications: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/875

Chicago Manual of Style (16th Edition):

Zhuang, Jiali. “Structural Variation Discovery and Genotyping from Whole Genome Sequencing: Methodology and Applications: A Dissertation.” 2015. Doctoral Dissertation, U of Massachusetts : Med. Accessed August 12, 2020. http://escholarship.umassmed.edu/gsbs_diss/875.

MLA Handbook (7th Edition):

Zhuang, Jiali. “Structural Variation Discovery and Genotyping from Whole Genome Sequencing: Methodology and Applications: A Dissertation.” 2015. Web. 12 Aug 2020.

Vancouver:

Zhuang J. Structural Variation Discovery and Genotyping from Whole Genome Sequencing: Methodology and Applications: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2015. [cited 2020 Aug 12]. Available from: http://escholarship.umassmed.edu/gsbs_diss/875.

Council of Science Editors:

Zhuang J. Structural Variation Discovery and Genotyping from Whole Genome Sequencing: Methodology and Applications: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2015. Available from: http://escholarship.umassmed.edu/gsbs_diss/875


University of Oxford

22. Willems, Nathalie. Molecular dynamics simulations of lipase-surface interactions.

Degree: PhD, 2016, University of Oxford

 Lipases are enzymes that play fundamental roles in fat digestion and metabolism, and function at the interface formed between hydrophobic molecules and the surrounding aqueous… (more)

Subjects/Keywords: 572; Biochemistry; Structural Biology; Computational Modelling; Physics; Membranes; Molecular Dynamics; Enzymes; Lipases; Surface Interactions

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APA (6th Edition):

Willems, N. (2016). Molecular dynamics simulations of lipase-surface interactions. (Doctoral Dissertation). University of Oxford. Retrieved from https://ora.ox.ac.uk/objects/uuid:7765c334-7c02-4190-a4b2-99ad315cfe52 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.724950

Chicago Manual of Style (16th Edition):

Willems, Nathalie. “Molecular dynamics simulations of lipase-surface interactions.” 2016. Doctoral Dissertation, University of Oxford. Accessed August 12, 2020. https://ora.ox.ac.uk/objects/uuid:7765c334-7c02-4190-a4b2-99ad315cfe52 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.724950.

MLA Handbook (7th Edition):

Willems, Nathalie. “Molecular dynamics simulations of lipase-surface interactions.” 2016. Web. 12 Aug 2020.

Vancouver:

Willems N. Molecular dynamics simulations of lipase-surface interactions. [Internet] [Doctoral dissertation]. University of Oxford; 2016. [cited 2020 Aug 12]. Available from: https://ora.ox.ac.uk/objects/uuid:7765c334-7c02-4190-a4b2-99ad315cfe52 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.724950.

Council of Science Editors:

Willems N. Molecular dynamics simulations of lipase-surface interactions. [Doctoral Dissertation]. University of Oxford; 2016. Available from: https://ora.ox.ac.uk/objects/uuid:7765c334-7c02-4190-a4b2-99ad315cfe52 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.724950


Utah State University

23. Lundell, Katie A. Electronic Transmutation: An Aid for the Rational Design of New Chemical Materials Using the Knowledge of Bonding and Structure of Neighboring Elements.

Degree: PhD, Chemistry and Biochemistry, 2019, Utah State University

  Everything in the universe is made up of elements from the periodic table. Each element has its own role that it plays in the… (more)

Subjects/Keywords: Electronic Transmutation; Theoretical Chemistry; Computational Chemistry; Molecular Ion Beam; Biochemistry, Biophysics, and Structural Biology; Chemistry

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APA (6th Edition):

Lundell, K. A. (2019). Electronic Transmutation: An Aid for the Rational Design of New Chemical Materials Using the Knowledge of Bonding and Structure of Neighboring Elements. (Doctoral Dissertation). Utah State University. Retrieved from https://digitalcommons.usu.edu/etd/7525

Chicago Manual of Style (16th Edition):

Lundell, Katie A. “Electronic Transmutation: An Aid for the Rational Design of New Chemical Materials Using the Knowledge of Bonding and Structure of Neighboring Elements.” 2019. Doctoral Dissertation, Utah State University. Accessed August 12, 2020. https://digitalcommons.usu.edu/etd/7525.

MLA Handbook (7th Edition):

Lundell, Katie A. “Electronic Transmutation: An Aid for the Rational Design of New Chemical Materials Using the Knowledge of Bonding and Structure of Neighboring Elements.” 2019. Web. 12 Aug 2020.

Vancouver:

Lundell KA. Electronic Transmutation: An Aid for the Rational Design of New Chemical Materials Using the Knowledge of Bonding and Structure of Neighboring Elements. [Internet] [Doctoral dissertation]. Utah State University; 2019. [cited 2020 Aug 12]. Available from: https://digitalcommons.usu.edu/etd/7525.

Council of Science Editors:

Lundell KA. Electronic Transmutation: An Aid for the Rational Design of New Chemical Materials Using the Knowledge of Bonding and Structure of Neighboring Elements. [Doctoral Dissertation]. Utah State University; 2019. Available from: https://digitalcommons.usu.edu/etd/7525


Virginia Commonwealth University

24. Norris, Shaun W. A Pipeline for Creation of Genome-Scale Metabolic Reconstructions.

Degree: MS, Bioinformatics, 2016, Virginia Commonwealth University

  The decreasing costs of next generation sequencing technologies and the increasing speeds at which they work have lead to an abundance of 'omic datasets.… (more)

Subjects/Keywords: Bioinformatics; metabolic reconstructions; metabolics; metmodel; asgard; flux balance analysis; Biochemistry; Bioinformatics; Computational Biology; Structural Biology; Systems Biology

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APA (6th Edition):

Norris, S. W. (2016). A Pipeline for Creation of Genome-Scale Metabolic Reconstructions. (Thesis). Virginia Commonwealth University. Retrieved from https://doi.org/10.25772/BP5V-EP74 ; https://scholarscompass.vcu.edu/etd/4667

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):

Norris, Shaun W. “A Pipeline for Creation of Genome-Scale Metabolic Reconstructions.” 2016. Thesis, Virginia Commonwealth University. Accessed August 12, 2020. https://doi.org/10.25772/BP5V-EP74 ; https://scholarscompass.vcu.edu/etd/4667.

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

MLA Handbook (7th Edition):

Norris, Shaun W. “A Pipeline for Creation of Genome-Scale Metabolic Reconstructions.” 2016. Web. 12 Aug 2020.

Vancouver:

Norris SW. A Pipeline for Creation of Genome-Scale Metabolic Reconstructions. [Internet] [Thesis]. Virginia Commonwealth University; 2016. [cited 2020 Aug 12]. Available from: https://doi.org/10.25772/BP5V-EP74 ; https://scholarscompass.vcu.edu/etd/4667.

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

Council of Science Editors:

Norris SW. A Pipeline for Creation of Genome-Scale Metabolic Reconstructions. [Thesis]. Virginia Commonwealth University; 2016. Available from: https://doi.org/10.25772/BP5V-EP74 ; https://scholarscompass.vcu.edu/etd/4667

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


Georgia Tech

25. Gossett, John Jared. Analysis of macromolecular structure through experiment and computation.

Degree: PhD, Computer Science, 2013, Georgia Tech

 This thesis covers a wide variety of projects within the domain of computational structural biology. Structural biology is concerned with the molecular structure of proteins… (more)

Subjects/Keywords: Computational biology; Structural biology; Molecular nanowire; Ribosomal RNA; Satellite tobacco mosaic virus; SHAPE chemistry; Macromolecular modeling; Data analysis; Macromolecules Analysis; Computational biology; Biomolecules Structure; Molecular dynamics; Computer simulation

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APA (6th Edition):

Gossett, J. J. (2013). Analysis of macromolecular structure through experiment and computation. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/51925

Chicago Manual of Style (16th Edition):

Gossett, John Jared. “Analysis of macromolecular structure through experiment and computation.” 2013. Doctoral Dissertation, Georgia Tech. Accessed August 12, 2020. http://hdl.handle.net/1853/51925.

MLA Handbook (7th Edition):

Gossett, John Jared. “Analysis of macromolecular structure through experiment and computation.” 2013. Web. 12 Aug 2020.

Vancouver:

Gossett JJ. Analysis of macromolecular structure through experiment and computation. [Internet] [Doctoral dissertation]. Georgia Tech; 2013. [cited 2020 Aug 12]. Available from: http://hdl.handle.net/1853/51925.

Council of Science Editors:

Gossett JJ. Analysis of macromolecular structure through experiment and computation. [Doctoral Dissertation]. Georgia Tech; 2013. Available from: http://hdl.handle.net/1853/51925


University of California – San Francisco

26. Kim, Michael F. Modeling Macromolecular Assemblies.

Degree: Biological and Medical Informatics, 2008, University of California – San Francisco

 Macromolecular assemblies are fundamental to most biological processes and here we attempt to improve the structural characterization of assemblies in the hopes that with new… (more)

Subjects/Keywords: Biology, Bioinformatics; Biophysics, General; computational structural biology

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APA (6th Edition):

Kim, M. F. (2008). Modeling Macromolecular Assemblies. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/08b67421

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):

Kim, Michael F. “Modeling Macromolecular Assemblies.” 2008. Thesis, University of California – San Francisco. Accessed August 12, 2020. http://www.escholarship.org/uc/item/08b67421.

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

MLA Handbook (7th Edition):

Kim, Michael F. “Modeling Macromolecular Assemblies.” 2008. Web. 12 Aug 2020.

Vancouver:

Kim MF. Modeling Macromolecular Assemblies. [Internet] [Thesis]. University of California – San Francisco; 2008. [cited 2020 Aug 12]. Available from: http://www.escholarship.org/uc/item/08b67421.

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

Council of Science Editors:

Kim MF. Modeling Macromolecular Assemblies. [Thesis]. University of California – San Francisco; 2008. Available from: http://www.escholarship.org/uc/item/08b67421

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


University of Washington

27. Bale, Jacob Barile. Computational design of co-assembling multi-component protein nanomaterials.

Degree: PhD, 2016, University of Washington

 Molecular self- and co-assembly of proteins into highly ordered symmetric complexes is an elegant and powerful means of patterning matter at the atomic scale and… (more)

Subjects/Keywords: co-assembly; computational protein design; nanomaterials; polyhedra; self-assembly; structural biology; Biochemistry; Nanoscience; Engineering; molecular and cellular biology

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APA (6th Edition):

Bale, J. B. (2016). Computational design of co-assembling multi-component protein nanomaterials. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/35263

Chicago Manual of Style (16th Edition):

Bale, Jacob Barile. “Computational design of co-assembling multi-component protein nanomaterials.” 2016. Doctoral Dissertation, University of Washington. Accessed August 12, 2020. http://hdl.handle.net/1773/35263.

MLA Handbook (7th Edition):

Bale, Jacob Barile. “Computational design of co-assembling multi-component protein nanomaterials.” 2016. Web. 12 Aug 2020.

Vancouver:

Bale JB. Computational design of co-assembling multi-component protein nanomaterials. [Internet] [Doctoral dissertation]. University of Washington; 2016. [cited 2020 Aug 12]. Available from: http://hdl.handle.net/1773/35263.

Council of Science Editors:

Bale JB. Computational design of co-assembling multi-component protein nanomaterials. [Doctoral Dissertation]. University of Washington; 2016. Available from: http://hdl.handle.net/1773/35263


Texas Medical Center

28. Paudyal, Nabina. LBPI: A WEB INTERFACE FOR THE IDENTIFICATION OF ALLOSTERIC LIGAND BINDING SITES.

Degree: MS, 2017, Texas Medical Center

  The development of efficient tools for allosteric ligand binding site identification in potential drug targets is an important step for computational drug design. Ligand… (more)

Subjects/Keywords: LBPI; Web Interface; Computational Pipeline; Wrapper; LIBSA; Python; Django; Platform; Integrate; Availability; Integrative Biology; Structural Biology

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APA (6th Edition):

Paudyal, N. (2017). LBPI: A WEB INTERFACE FOR THE IDENTIFICATION OF ALLOSTERIC LIGAND BINDING SITES. (Thesis). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/792

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):

Paudyal, Nabina. “LBPI: A WEB INTERFACE FOR THE IDENTIFICATION OF ALLOSTERIC LIGAND BINDING SITES.” 2017. Thesis, Texas Medical Center. Accessed August 12, 2020. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/792.

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

MLA Handbook (7th Edition):

Paudyal, Nabina. “LBPI: A WEB INTERFACE FOR THE IDENTIFICATION OF ALLOSTERIC LIGAND BINDING SITES.” 2017. Web. 12 Aug 2020.

Vancouver:

Paudyal N. LBPI: A WEB INTERFACE FOR THE IDENTIFICATION OF ALLOSTERIC LIGAND BINDING SITES. [Internet] [Thesis]. Texas Medical Center; 2017. [cited 2020 Aug 12]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/792.

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

Council of Science Editors:

Paudyal N. LBPI: A WEB INTERFACE FOR THE IDENTIFICATION OF ALLOSTERIC LIGAND BINDING SITES. [Thesis]. Texas Medical Center; 2017. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/792

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

29. Jiang, Li. Systematic Experimental Determination of Functional Constraints on Proteins and Adaptive Potential of Mutations: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2016, U of Massachusetts : Med

  Sequence-function relationship is a fundamental question for many branches of modern biomedical research. It connects the primary sequence of proteins to the function of… (more)

Subjects/Keywords: Viral Proteins; Genomics; High-Throughput Nucleotide Sequencing; RNA Sequence Analysis; Mutation; Computational Biology; Ecology and Evolutionary Biology; Genomics; Molecular Biology; Structural Biology; Systems Biology

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APA (6th Edition):

Jiang, L. (2016). Systematic Experimental Determination of Functional Constraints on Proteins and Adaptive Potential of Mutations: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/854

Chicago Manual of Style (16th Edition):

Jiang, Li. “Systematic Experimental Determination of Functional Constraints on Proteins and Adaptive Potential of Mutations: A Dissertation.” 2016. Doctoral Dissertation, U of Massachusetts : Med. Accessed August 12, 2020. http://escholarship.umassmed.edu/gsbs_diss/854.

MLA Handbook (7th Edition):

Jiang, Li. “Systematic Experimental Determination of Functional Constraints on Proteins and Adaptive Potential of Mutations: A Dissertation.” 2016. Web. 12 Aug 2020.

Vancouver:

Jiang L. Systematic Experimental Determination of Functional Constraints on Proteins and Adaptive Potential of Mutations: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2016. [cited 2020 Aug 12]. Available from: http://escholarship.umassmed.edu/gsbs_diss/854.

Council of Science Editors:

Jiang L. Systematic Experimental Determination of Functional Constraints on Proteins and Adaptive Potential of Mutations: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2016. Available from: http://escholarship.umassmed.edu/gsbs_diss/854


Texas Medical Center

30. Paudyal, Nabina. LBPI: A WEB INTERFACE FOR THE IDENTIFICATION OF ALLOSTERIC LIGAND BINDING SITES.

Degree: MS, 2017, Texas Medical Center

  The development of efficient tools for allosteric ligand binding site identification in potential drug targets is an important step for computational drug design. Ligand… (more)

Subjects/Keywords: LBPI; Web Interface; Computational Pipeline; Wrapper; LIBSA; Python; Django; Platform; Integrate; Availability; Biochemistry, Biophysics, and Structural Biology

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

APA (6th Edition):

Paudyal, N. (2017). LBPI: A WEB INTERFACE FOR THE IDENTIFICATION OF ALLOSTERIC LIGAND BINDING SITES. (Thesis). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/830

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):

Paudyal, Nabina. “LBPI: A WEB INTERFACE FOR THE IDENTIFICATION OF ALLOSTERIC LIGAND BINDING SITES.” 2017. Thesis, Texas Medical Center. Accessed August 12, 2020. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/830.

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

MLA Handbook (7th Edition):

Paudyal, Nabina. “LBPI: A WEB INTERFACE FOR THE IDENTIFICATION OF ALLOSTERIC LIGAND BINDING SITES.” 2017. Web. 12 Aug 2020.

Vancouver:

Paudyal N. LBPI: A WEB INTERFACE FOR THE IDENTIFICATION OF ALLOSTERIC LIGAND BINDING SITES. [Internet] [Thesis]. Texas Medical Center; 2017. [cited 2020 Aug 12]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/830.

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

Council of Science Editors:

Paudyal N. LBPI: A WEB INTERFACE FOR THE IDENTIFICATION OF ALLOSTERIC LIGAND BINDING SITES. [Thesis]. Texas Medical Center; 2017. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/830

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

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