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You searched for +publisher:"Georgia Tech" +contributor:("Williams, Loren"). Showing records 1 – 30 of 59 total matches.

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1. Kovacs, Nicholas Attila. Data mining the structure of the ribosome to unravel the history of proteins.

Degree: PhD, Chemistry and Biochemistry, 2018, Georgia Tech

 Contained within every cell of every organism on Earth is a molecular fossil that has recorded the evolution of life since its origin approximately 4… (more)

Subjects/Keywords: Ribosome; Protein; Structural bioinformatics

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APA (6th Edition):

Kovacs, N. A. (2018). Data mining the structure of the ribosome to unravel the history of proteins. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60789

Chicago Manual of Style (16th Edition):

Kovacs, Nicholas Attila. “Data mining the structure of the ribosome to unravel the history of proteins.” 2018. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/60789.

MLA Handbook (7th Edition):

Kovacs, Nicholas Attila. “Data mining the structure of the ribosome to unravel the history of proteins.” 2018. Web. 19 Jan 2021.

Vancouver:

Kovacs NA. Data mining the structure of the ribosome to unravel the history of proteins. [Internet] [Doctoral dissertation]. Georgia Tech; 2018. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/60789.

Council of Science Editors:

Kovacs NA. Data mining the structure of the ribosome to unravel the history of proteins. [Doctoral Dissertation]. Georgia Tech; 2018. Available from: http://hdl.handle.net/1853/60789


Georgia Tech

2. Laughlin, Brandon Patrick. Characterization of DNA duplex structure, stability and formation kinetics in a eutectic solvent and its aqueous mixtures.

Degree: MS, Chemistry and Biochemistry, 2015, Georgia Tech

 In this work, properties and behavior of DNA oligonucleotides in a non-aqueous eutectic comprised of glycerol and choline chloride mixed at varying ratios, as well… (more)

Subjects/Keywords: Eutectics; DNA; Kinetics; Thermodynamics

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APA (6th Edition):

Laughlin, B. P. (2015). Characterization of DNA duplex structure, stability and formation kinetics in a eutectic solvent and its aqueous mixtures. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60387

Chicago Manual of Style (16th Edition):

Laughlin, Brandon Patrick. “Characterization of DNA duplex structure, stability and formation kinetics in a eutectic solvent and its aqueous mixtures.” 2015. Masters Thesis, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/60387.

MLA Handbook (7th Edition):

Laughlin, Brandon Patrick. “Characterization of DNA duplex structure, stability and formation kinetics in a eutectic solvent and its aqueous mixtures.” 2015. Web. 19 Jan 2021.

Vancouver:

Laughlin BP. Characterization of DNA duplex structure, stability and formation kinetics in a eutectic solvent and its aqueous mixtures. [Internet] [Masters thesis]. Georgia Tech; 2015. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/60387.

Council of Science Editors:

Laughlin BP. Characterization of DNA duplex structure, stability and formation kinetics in a eutectic solvent and its aqueous mixtures. [Masters Thesis]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/60387


Georgia Tech

3. Bachman, Haylee N. Exploring fibronectin's integrin binding domain effects on lung fibroblast integrin specificity and downstream phenotypic differences.

Degree: PhD, Chemistry and Biochemistry, 2017, Georgia Tech

 Recombinant proteins which mimic fibronectin’s (Fn’s) integrin binding domain in conformationally stable and unfolded states are investigated to explore integrin specificity and downstream phenotypic differences… (more)

Subjects/Keywords: Fibronectin; Integrin; Mechanobiology; Matrix biology; Extracellular matrix

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APA (6th Edition):

Bachman, H. N. (2017). Exploring fibronectin's integrin binding domain effects on lung fibroblast integrin specificity and downstream phenotypic differences. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60669

Chicago Manual of Style (16th Edition):

Bachman, Haylee N. “Exploring fibronectin's integrin binding domain effects on lung fibroblast integrin specificity and downstream phenotypic differences.” 2017. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/60669.

MLA Handbook (7th Edition):

Bachman, Haylee N. “Exploring fibronectin's integrin binding domain effects on lung fibroblast integrin specificity and downstream phenotypic differences.” 2017. Web. 19 Jan 2021.

Vancouver:

Bachman HN. Exploring fibronectin's integrin binding domain effects on lung fibroblast integrin specificity and downstream phenotypic differences. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/60669.

Council of Science Editors:

Bachman HN. Exploring fibronectin's integrin binding domain effects on lung fibroblast integrin specificity and downstream phenotypic differences. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/60669


Georgia Tech

4. Balusek, Curtis A. Pushing the cell envelope: Simulations at the gram-negative cellular interface.

Degree: PhD, Physics, 2019, Georgia Tech

 Computational simulations of bacterial membrane systems were performed in silico using molecular dynamics to describe the function and interaction of integral, membrane-spanning proteins with their… (more)

Subjects/Keywords: Gram-negative; Simulation; Outer-membrane; Hydrogen mass repartitioning; Cell envelope

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APA (6th Edition):

Balusek, C. A. (2019). Pushing the cell envelope: Simulations at the gram-negative cellular interface. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/62639

Chicago Manual of Style (16th Edition):

Balusek, Curtis A. “Pushing the cell envelope: Simulations at the gram-negative cellular interface.” 2019. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/62639.

MLA Handbook (7th Edition):

Balusek, Curtis A. “Pushing the cell envelope: Simulations at the gram-negative cellular interface.” 2019. Web. 19 Jan 2021.

Vancouver:

Balusek CA. Pushing the cell envelope: Simulations at the gram-negative cellular interface. [Internet] [Doctoral dissertation]. Georgia Tech; 2019. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/62639.

Council of Science Editors:

Balusek CA. Pushing the cell envelope: Simulations at the gram-negative cellular interface. [Doctoral Dissertation]. Georgia Tech; 2019. Available from: http://hdl.handle.net/1853/62639


Georgia Tech

5. Patterson-Orazem, Athena Capucine. Development of conformational myocilin antibodies, and biophysical characterisation of the mouse myocilin olfactomedin domain.

Degree: PhD, Chemistry and Biochemistry, 2019, Georgia Tech

 Mutations in myocilin are causative for the heritable form of open angle glaucoma in humans yet, almost 20 years after its discovery, the function of… (more)

Subjects/Keywords: Myocilin; Glaucoma; Antibodies; Biophysical; Protein; Structure; Function; Aggregation

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APA (6th Edition):

Patterson-Orazem, A. C. (2019). Development of conformational myocilin antibodies, and biophysical characterisation of the mouse myocilin olfactomedin domain. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/62671

Chicago Manual of Style (16th Edition):

Patterson-Orazem, Athena Capucine. “Development of conformational myocilin antibodies, and biophysical characterisation of the mouse myocilin olfactomedin domain.” 2019. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/62671.

MLA Handbook (7th Edition):

Patterson-Orazem, Athena Capucine. “Development of conformational myocilin antibodies, and biophysical characterisation of the mouse myocilin olfactomedin domain.” 2019. Web. 19 Jan 2021.

Vancouver:

Patterson-Orazem AC. Development of conformational myocilin antibodies, and biophysical characterisation of the mouse myocilin olfactomedin domain. [Internet] [Doctoral dissertation]. Georgia Tech; 2019. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/62671.

Council of Science Editors:

Patterson-Orazem AC. Development of conformational myocilin antibodies, and biophysical characterisation of the mouse myocilin olfactomedin domain. [Doctoral Dissertation]. Georgia Tech; 2019. Available from: http://hdl.handle.net/1853/62671


Georgia Tech

6. Walker, Christopher L. Green fluorescent protein inspired chromophore as estrogen receptor agonist-synthesis, biological evaluations and cellular application.

Degree: PhD, Chemistry and Biochemistry, 2019, Georgia Tech

 Nuclear receptors are ligand activated transcription factors that are widely distributed throughout the mammalians. There are 48 known human nuclear receptors within the body located… (more)

Subjects/Keywords: Estrogen receptor

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APA (6th Edition):

Walker, C. L. (2019). Green fluorescent protein inspired chromophore as estrogen receptor agonist-synthesis, biological evaluations and cellular application. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/61211

Chicago Manual of Style (16th Edition):

Walker, Christopher L. “Green fluorescent protein inspired chromophore as estrogen receptor agonist-synthesis, biological evaluations and cellular application.” 2019. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/61211.

MLA Handbook (7th Edition):

Walker, Christopher L. “Green fluorescent protein inspired chromophore as estrogen receptor agonist-synthesis, biological evaluations and cellular application.” 2019. Web. 19 Jan 2021.

Vancouver:

Walker CL. Green fluorescent protein inspired chromophore as estrogen receptor agonist-synthesis, biological evaluations and cellular application. [Internet] [Doctoral dissertation]. Georgia Tech; 2019. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/61211.

Council of Science Editors:

Walker CL. Green fluorescent protein inspired chromophore as estrogen receptor agonist-synthesis, biological evaluations and cellular application. [Doctoral Dissertation]. Georgia Tech; 2019. Available from: http://hdl.handle.net/1853/61211


Georgia Tech

7. Johnson, Matthew C. Identifying key factors in two-dimensional crystal production and sample preparation for structure-function studies of membrane proteins by cryo-EM.

Degree: PhD, Biology, 2013, Georgia Tech

 Electron crystallography of two-dimensional crystals is a structure-determination method well suited to the study of membrane protein structure-function. Two-dimensional crystals consist of ordered arrays of… (more)

Subjects/Keywords: Membrane protein; Protein structure; Cryo-EM; Electron microscopy; Electron cryo-microscopy; Electron crystallography; Two-dimensional crystallization; LTC₄S; Leukotriene C₄ Synthase; Gamma-glutamyl carboxylase; GGCX

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APA (6th Edition):

Johnson, M. C. (2013). Identifying key factors in two-dimensional crystal production and sample preparation for structure-function studies of membrane proteins by cryo-EM. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/52974

Chicago Manual of Style (16th Edition):

Johnson, Matthew C. “Identifying key factors in two-dimensional crystal production and sample preparation for structure-function studies of membrane proteins by cryo-EM.” 2013. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/52974.

MLA Handbook (7th Edition):

Johnson, Matthew C. “Identifying key factors in two-dimensional crystal production and sample preparation for structure-function studies of membrane proteins by cryo-EM.” 2013. Web. 19 Jan 2021.

Vancouver:

Johnson MC. Identifying key factors in two-dimensional crystal production and sample preparation for structure-function studies of membrane proteins by cryo-EM. [Internet] [Doctoral dissertation]. Georgia Tech; 2013. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/52974.

Council of Science Editors:

Johnson MC. Identifying key factors in two-dimensional crystal production and sample preparation for structure-function studies of membrane proteins by cryo-EM. [Doctoral Dissertation]. Georgia Tech; 2013. Available from: http://hdl.handle.net/1853/52974


Georgia Tech

8. Kalyoncu, Sibel. Structural and functional characterization of an intramembrane peptidase and a non-peptidase homolog.

Degree: PhD, Chemistry and Biochemistry, 2016, Georgia Tech

 Peptidases play fundamental roles in all living organisms and their dysfunction is associated with a variety of diseases. Although sequences of peptidases encoded in genomes… (more)

Subjects/Keywords: Protein; Peptidase; Crystallization; Biochemistry; Nitroaromatics

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APA (6th Edition):

Kalyoncu, S. (2016). Structural and functional characterization of an intramembrane peptidase and a non-peptidase homolog. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58584

Chicago Manual of Style (16th Edition):

Kalyoncu, Sibel. “Structural and functional characterization of an intramembrane peptidase and a non-peptidase homolog.” 2016. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/58584.

MLA Handbook (7th Edition):

Kalyoncu, Sibel. “Structural and functional characterization of an intramembrane peptidase and a non-peptidase homolog.” 2016. Web. 19 Jan 2021.

Vancouver:

Kalyoncu S. Structural and functional characterization of an intramembrane peptidase and a non-peptidase homolog. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/58584.

Council of Science Editors:

Kalyoncu S. Structural and functional characterization of an intramembrane peptidase and a non-peptidase homolog. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/58584


Georgia Tech

9. Parker, Eric Thomas. New insights into biomolecule polymerization under plausible primordial earth conditions: Implications for the origin of life.

Degree: PhD, Chemistry and Biochemistry, 2016, Georgia Tech

 The origin of life on Earth is amongst the greatest scientific mysteries. The Miller-Urey experiment brought legitimacy to studying life's origins and ushered in the… (more)

Subjects/Keywords: Electric discharge; Titan chemistry; Cyanamide; Dipeptide; Diketopiperazine; Alpha-hydroxy acid; Ultra high performance liquid chromatography; Triple quadrupole mass spectrometry; Depsipeptide; Ion-pair chromatography; Traveling wave ion mobility spectrometry; High resolution tandem mass spectrometry

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APA (6th Edition):

Parker, E. T. (2016). New insights into biomolecule polymerization under plausible primordial earth conditions: Implications for the origin of life. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58621

Chicago Manual of Style (16th Edition):

Parker, Eric Thomas. “New insights into biomolecule polymerization under plausible primordial earth conditions: Implications for the origin of life.” 2016. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/58621.

MLA Handbook (7th Edition):

Parker, Eric Thomas. “New insights into biomolecule polymerization under plausible primordial earth conditions: Implications for the origin of life.” 2016. Web. 19 Jan 2021.

Vancouver:

Parker ET. New insights into biomolecule polymerization under plausible primordial earth conditions: Implications for the origin of life. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/58621.

Council of Science Editors:

Parker ET. New insights into biomolecule polymerization under plausible primordial earth conditions: Implications for the origin of life. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/58621


Georgia Tech

10. 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 January 19, 2021. http://hdl.handle.net/1853/51925.

MLA Handbook (7th Edition):

Gossett, John Jared. “Analysis of macromolecular structure through experiment and computation.” 2013. Web. 19 Jan 2021.

Vancouver:

Gossett JJ. Analysis of macromolecular structure through experiment and computation. [Internet] [Doctoral dissertation]. Georgia Tech; 2013. [cited 2021 Jan 19]. 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


Georgia Tech

11. Washington, Arren Z. The development and evaluation of small molecule-peptide conjugates as probes of prokaryotic ribosome exit tunnel-nascent peptide interaction.

Degree: PhD, Chemistry and Biochemistry, 2016, Georgia Tech

 As the knowledge base grows in regard to peptide synthesis and ribosomal actions, one facet of this is the extent and selectivity of interactions between… (more)

Subjects/Keywords: Prokaryotic ribosome; Ribosomal exit tunnel; Antibiotics; Probe interactions; Peptide; Peptoid

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APA (6th Edition):

Washington, A. Z. (2016). The development and evaluation of small molecule-peptide conjugates as probes of prokaryotic ribosome exit tunnel-nascent peptide interaction. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/59116

Chicago Manual of Style (16th Edition):

Washington, Arren Z. “The development and evaluation of small molecule-peptide conjugates as probes of prokaryotic ribosome exit tunnel-nascent peptide interaction.” 2016. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/59116.

MLA Handbook (7th Edition):

Washington, Arren Z. “The development and evaluation of small molecule-peptide conjugates as probes of prokaryotic ribosome exit tunnel-nascent peptide interaction.” 2016. Web. 19 Jan 2021.

Vancouver:

Washington AZ. The development and evaluation of small molecule-peptide conjugates as probes of prokaryotic ribosome exit tunnel-nascent peptide interaction. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/59116.

Council of Science Editors:

Washington AZ. The development and evaluation of small molecule-peptide conjugates as probes of prokaryotic ribosome exit tunnel-nascent peptide interaction. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/59116

12. Ali, Moustafa Ragab. Development and molecular understanding of plasmonic photothermal therapy (PPTT) in combating cancer.

Degree: PhD, Chemistry and Biochemistry, 2017, Georgia Tech

 In cancer plasmonic photothermal therapy (PPTT), gold nanoparticles (AuNPs) are used to convert light energy into localized heat leading to cancer cell death. Among plasmonic… (more)

Subjects/Keywords: Progress in Plasmonic photothermal therapy; Nanomedicine

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APA (6th Edition):

Ali, M. R. (2017). Development and molecular understanding of plasmonic photothermal therapy (PPTT) in combating cancer. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/59792

Chicago Manual of Style (16th Edition):

Ali, Moustafa Ragab. “Development and molecular understanding of plasmonic photothermal therapy (PPTT) in combating cancer.” 2017. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/59792.

MLA Handbook (7th Edition):

Ali, Moustafa Ragab. “Development and molecular understanding of plasmonic photothermal therapy (PPTT) in combating cancer.” 2017. Web. 19 Jan 2021.

Vancouver:

Ali MR. Development and molecular understanding of plasmonic photothermal therapy (PPTT) in combating cancer. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/59792.

Council of Science Editors:

Ali MR. Development and molecular understanding of plasmonic photothermal therapy (PPTT) in combating cancer. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/59792


Georgia Tech

13. Crooke, Stephen Nicholas. Chemical and genetic modification of virus-like particles for applications in vaccine design and drug delivery.

Degree: PhD, Chemistry and Biochemistry, 2018, Georgia Tech

 Virus-like particles (VLPs) are multi-subunit protein assemblies that self-assemble into homogenous particles with periodic structure, making them ideal candidates for applications in biomedicine. This dissertation… (more)

Subjects/Keywords: Virus-like particles; Drug delivery; Vaccine design; Prodrug therapy; Protein-polymer materials

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APA (6th Edition):

Crooke, S. N. (2018). Chemical and genetic modification of virus-like particles for applications in vaccine design and drug delivery. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60247

Chicago Manual of Style (16th Edition):

Crooke, Stephen Nicholas. “Chemical and genetic modification of virus-like particles for applications in vaccine design and drug delivery.” 2018. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/60247.

MLA Handbook (7th Edition):

Crooke, Stephen Nicholas. “Chemical and genetic modification of virus-like particles for applications in vaccine design and drug delivery.” 2018. Web. 19 Jan 2021.

Vancouver:

Crooke SN. Chemical and genetic modification of virus-like particles for applications in vaccine design and drug delivery. [Internet] [Doctoral dissertation]. Georgia Tech; 2018. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/60247.

Council of Science Editors:

Crooke SN. Chemical and genetic modification of virus-like particles for applications in vaccine design and drug delivery. [Doctoral Dissertation]. Georgia Tech; 2018. Available from: http://hdl.handle.net/1853/60247


Georgia Tech

14. Ehrenworth, Amy M. Modified monoterpene indole alkaloid production in the yeast Saccharomyces cerevisiae.

Degree: PhD, Chemistry and Biochemistry, 2017, Georgia Tech

 Alkaloids are a large group of plant natural products that have important therapeutic value. Because of their chemical complexity, therapeutic alkaloids are often obtained via… (more)

Subjects/Keywords: Yeast; Saccharomyces cerevisiae; Alkaloids; Monoterpene indole alkaloids; Synthetic biology; Compartmentalization; Tetrahydrobiopterin; Natural product biosynthesis; Hydroxystrictosidine; Serotonin; Metabolic engineering; GPCR; Biosensor

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APA (6th Edition):

Ehrenworth, A. M. (2017). Modified monoterpene indole alkaloid production in the yeast Saccharomyces cerevisiae. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60672

Chicago Manual of Style (16th Edition):

Ehrenworth, Amy M. “Modified monoterpene indole alkaloid production in the yeast Saccharomyces cerevisiae.” 2017. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/60672.

MLA Handbook (7th Edition):

Ehrenworth, Amy M. “Modified monoterpene indole alkaloid production in the yeast Saccharomyces cerevisiae.” 2017. Web. 19 Jan 2021.

Vancouver:

Ehrenworth AM. Modified monoterpene indole alkaloid production in the yeast Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/60672.

Council of Science Editors:

Ehrenworth AM. Modified monoterpene indole alkaloid production in the yeast Saccharomyces cerevisiae. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/60672


Georgia Tech

15. Donegan, Rebecca Kristen. Structural and biophysical characterization of the myocilin olfactomedin domain.

Degree: PhD, Chemistry and Biochemistry, 2015, Georgia Tech

 The myocilin olfactomedin domain (myoc-OLF) is linked to inherited forms of open angle glaucoma. Mutant myocilin accumulates within the endoplasmic reticulum of human trabecular meshwork… (more)

Subjects/Keywords: Myocilin; Olfactomedin; Protein crystallography

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APA (6th Edition):

Donegan, R. K. (2015). Structural and biophysical characterization of the myocilin olfactomedin domain. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53872

Chicago Manual of Style (16th Edition):

Donegan, Rebecca Kristen. “Structural and biophysical characterization of the myocilin olfactomedin domain.” 2015. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/53872.

MLA Handbook (7th Edition):

Donegan, Rebecca Kristen. “Structural and biophysical characterization of the myocilin olfactomedin domain.” 2015. Web. 19 Jan 2021.

Vancouver:

Donegan RK. Structural and biophysical characterization of the myocilin olfactomedin domain. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/53872.

Council of Science Editors:

Donegan RK. Structural and biophysical characterization of the myocilin olfactomedin domain. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/53872


Georgia Tech

16. Le, Tung T. Single-molecule biophysics of DNA bending: looping and unlooping.

Degree: PhD, Physics, 2015, Georgia Tech

 DNA bending plays a vital role in numerous cellular activities such as transcription, viral packaging, and nucleosome formation. Therefore, understanding the physics of DNA bending… (more)

Subjects/Keywords: FRET; DNA flexibility; DNA bending; Worm-like chain; Cyclization

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APA (6th Edition):

Le, T. T. (2015). Single-molecule biophysics of DNA bending: looping and unlooping. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53979

Chicago Manual of Style (16th Edition):

Le, Tung T. “Single-molecule biophysics of DNA bending: looping and unlooping.” 2015. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/53979.

MLA Handbook (7th Edition):

Le, Tung T. “Single-molecule biophysics of DNA bending: looping and unlooping.” 2015. Web. 19 Jan 2021.

Vancouver:

Le TT. Single-molecule biophysics of DNA bending: looping and unlooping. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/53979.

Council of Science Editors:

Le TT. Single-molecule biophysics of DNA bending: looping and unlooping. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/53979


Georgia Tech

17. Meng, Xianzhi. Assessing the effect of pretreatment on cellulose accessibility for cellulosic biofuels production.

Degree: PhD, Chemistry and Biochemistry, 2015, Georgia Tech

 Biomass recalcitrance has been recognized as one of the major barriers that hided the cost-effective conversion of lignocellulosic biomass to bioethanol, therefore the current bioconversion… (more)

Subjects/Keywords: Biomass recalcitrance; Pretreatment; Cellulose accessibility; Simons' stain; Cellulose degree of polymerization; Cellulose crystallinity

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APA (6th Edition):

Meng, X. (2015). Assessing the effect of pretreatment on cellulose accessibility for cellulosic biofuels production. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54347

Chicago Manual of Style (16th Edition):

Meng, Xianzhi. “Assessing the effect of pretreatment on cellulose accessibility for cellulosic biofuels production.” 2015. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/54347.

MLA Handbook (7th Edition):

Meng, Xianzhi. “Assessing the effect of pretreatment on cellulose accessibility for cellulosic biofuels production.” 2015. Web. 19 Jan 2021.

Vancouver:

Meng X. Assessing the effect of pretreatment on cellulose accessibility for cellulosic biofuels production. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/54347.

Council of Science Editors:

Meng X. Assessing the effect of pretreatment on cellulose accessibility for cellulosic biofuels production. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/54347


Georgia Tech

18. Cafferty, Brian Joseph. Self-assembly of nucleobase analogs in water: supramolecular polymers, controllable materials and models for proto-nucleic acid.

Degree: PhD, Chemistry and Biochemistry, 2015, Georgia Tech

 Reversible self-assembly in water of small molecules into ordered structures is an essential process that underlies many biological functions and developmental strategies for environmentally responsive… (more)

Subjects/Keywords: Supramolecular polymers; Self-assembly in water; Supramolecular chemistry; Supramolecular materials; Biomimetic materials; Responsive materials; Hydrogels; Molecular gels; Noncovalent synthesis; Hydrophobic effect; Nanotechnology; DNA nanotechnology; Origin of life; Origins of life; RNA world; Pre-RNA world; Nucleoside synthesis; Nucleic acids; Modified nucleic acids; Alternative nucleic acids; Antisense oligonucleotides; XNA; Intercalators; Abiogenesis; Astrobiology

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APA (6th Edition):

Cafferty, B. J. (2015). Self-assembly of nucleobase analogs in water: supramolecular polymers, controllable materials and models for proto-nucleic acid. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/55518

Chicago Manual of Style (16th Edition):

Cafferty, Brian Joseph. “Self-assembly of nucleobase analogs in water: supramolecular polymers, controllable materials and models for proto-nucleic acid.” 2015. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/55518.

MLA Handbook (7th Edition):

Cafferty, Brian Joseph. “Self-assembly of nucleobase analogs in water: supramolecular polymers, controllable materials and models for proto-nucleic acid.” 2015. Web. 19 Jan 2021.

Vancouver:

Cafferty BJ. Self-assembly of nucleobase analogs in water: supramolecular polymers, controllable materials and models for proto-nucleic acid. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/55518.

Council of Science Editors:

Cafferty BJ. Self-assembly of nucleobase analogs in water: supramolecular polymers, controllable materials and models for proto-nucleic acid. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/55518


Georgia Tech

19. DeLey Cox, Vanessa E. Engineering elongation factor Tu and tRNAs to better accommodate non-canonical amino acids during translation.

Degree: PhD, Chemistry and Biochemistry, 2018, Georgia Tech

 Non-canonical amino acid (ncAA) incorporation has led to significant advances in protein science and engineering. Traditionally, incorporation of ncAAs is achieved via amber codon suppression… (more)

Subjects/Keywords: EF-Tu; Non-canonical amino acid; Orthogonal translation system; Genetic code expansion; Polyspecificity; Protein engineering; Ribosomal translation; Elongation factors

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APA (6th Edition):

DeLey Cox, V. E. (2018). Engineering elongation factor Tu and tRNAs to better accommodate non-canonical amino acids during translation. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/63483

Chicago Manual of Style (16th Edition):

DeLey Cox, Vanessa E. “Engineering elongation factor Tu and tRNAs to better accommodate non-canonical amino acids during translation.” 2018. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/63483.

MLA Handbook (7th Edition):

DeLey Cox, Vanessa E. “Engineering elongation factor Tu and tRNAs to better accommodate non-canonical amino acids during translation.” 2018. Web. 19 Jan 2021.

Vancouver:

DeLey Cox VE. Engineering elongation factor Tu and tRNAs to better accommodate non-canonical amino acids during translation. [Internet] [Doctoral dissertation]. Georgia Tech; 2018. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/63483.

Council of Science Editors:

DeLey Cox VE. Engineering elongation factor Tu and tRNAs to better accommodate non-canonical amino acids during translation. [Doctoral Dissertation]. Georgia Tech; 2018. Available from: http://hdl.handle.net/1853/63483


Georgia Tech

20. Fang, Po-Yu. Using QB VLPS to package, protect, and deliver in vivo produced RNAS.

Degree: PhD, Chemistry and Biochemistry, 2016, Georgia Tech

 This project focuses on Using Qβ VLPs to package, protect, and deliver recombinantly produced RNAs. The ultimate goal is to develop an RNA interference (RNAi)… (more)

Subjects/Keywords: Virus-like particles; RNAi; Gene regulation; RNA protection

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APA (6th Edition):

Fang, P. (2016). Using QB VLPS to package, protect, and deliver in vivo produced RNAS. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58592

Chicago Manual of Style (16th Edition):

Fang, Po-Yu. “Using QB VLPS to package, protect, and deliver in vivo produced RNAS.” 2016. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/58592.

MLA Handbook (7th Edition):

Fang, Po-Yu. “Using QB VLPS to package, protect, and deliver in vivo produced RNAS.” 2016. Web. 19 Jan 2021.

Vancouver:

Fang P. Using QB VLPS to package, protect, and deliver in vivo produced RNAS. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/58592.

Council of Science Editors:

Fang P. Using QB VLPS to package, protect, and deliver in vivo produced RNAS. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/58592


Georgia Tech

21. Kratzer, James Timothy. Reengineering a human-like uricase for the treatment of gout.

Degree: PhD, Chemistry and Biochemistry, 2013, Georgia Tech

 There is an unmet medical need in the treatment of gout. This type of inflammatory arthritis can be efficiently alleviated by the enzyme uricase. This… (more)

Subjects/Keywords: Gout; Uricase; Ancestral sequence reconstruction; Protein engineering; Evolutionary synthetic biology; Pseudogene; Enzyme replacement; Therapy; Enzyme assays; Protein purification; Pharmacokinetics; Protein solubility; Evolution

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APA (6th Edition):

Kratzer, J. T. (2013). Reengineering a human-like uricase for the treatment of gout. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/52149

Chicago Manual of Style (16th Edition):

Kratzer, James Timothy. “Reengineering a human-like uricase for the treatment of gout.” 2013. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/52149.

MLA Handbook (7th Edition):

Kratzer, James Timothy. “Reengineering a human-like uricase for the treatment of gout.” 2013. Web. 19 Jan 2021.

Vancouver:

Kratzer JT. Reengineering a human-like uricase for the treatment of gout. [Internet] [Doctoral dissertation]. Georgia Tech; 2013. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/52149.

Council of Science Editors:

Kratzer JT. Reengineering a human-like uricase for the treatment of gout. [Doctoral Dissertation]. Georgia Tech; 2013. Available from: http://hdl.handle.net/1853/52149


Georgia Tech

22. Bernier, Chad R. Evolution of the ribosomal common core.

Degree: PhD, Chemistry and Biochemistry, 2014, Georgia Tech

 Understanding the origin of life requires understanding the origin of translation, which in turn, requires understanding the origin of the ribosome. Ribosomes are complex structures… (more)

Subjects/Keywords: Ribosome; Evolution

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APA (6th Edition):

Bernier, C. R. (2014). Evolution of the ribosomal common core. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54306

Chicago Manual of Style (16th Edition):

Bernier, Chad R. “Evolution of the ribosomal common core.” 2014. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/54306.

MLA Handbook (7th Edition):

Bernier, Chad R. “Evolution of the ribosomal common core.” 2014. Web. 19 Jan 2021.

Vancouver:

Bernier CR. Evolution of the ribosomal common core. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/54306.

Council of Science Editors:

Bernier CR. Evolution of the ribosomal common core. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/54306


Georgia Tech

23. Mestre Fos, Santiago. Non-canonical structures and functions of the human ribosome: G-quadruplexes and heme appropriation.

Degree: PhD, Chemistry and Biochemistry, 2020, Georgia Tech

 The ribosome is a macromolecular ribonucleoprotein machine that is responsible for the synthesis of all proteins in cells. Mammalian ribosomal RNAs (rRNAs) are nearly twice… (more)

Subjects/Keywords: Ribosome; RNA; Heme; G-quadruplex; rRNA; Expansion segments

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APA (6th Edition):

Mestre Fos, S. (2020). Non-canonical structures and functions of the human ribosome: G-quadruplexes and heme appropriation. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/63645

Chicago Manual of Style (16th Edition):

Mestre Fos, Santiago. “Non-canonical structures and functions of the human ribosome: G-quadruplexes and heme appropriation.” 2020. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/63645.

MLA Handbook (7th Edition):

Mestre Fos, Santiago. “Non-canonical structures and functions of the human ribosome: G-quadruplexes and heme appropriation.” 2020. Web. 19 Jan 2021.

Vancouver:

Mestre Fos S. Non-canonical structures and functions of the human ribosome: G-quadruplexes and heme appropriation. [Internet] [Doctoral dissertation]. Georgia Tech; 2020. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/63645.

Council of Science Editors:

Mestre Fos S. Non-canonical structures and functions of the human ribosome: G-quadruplexes and heme appropriation. [Doctoral Dissertation]. Georgia Tech; 2020. Available from: http://hdl.handle.net/1853/63645

24. Lannan, Ford. Folding of the human telomere sequence DNA in non-aqueous and otherwise viscous solvents.

Degree: MS, Chemistry and Biochemistry, 2012, Georgia Tech

 G-quadruplex forming human telomere sequence (HTS) DNA, has been widely studied due to the telomere's implied role in biological processes, including cellular ageing and cancer… (more)

Subjects/Keywords: G-quadruplex; Kinetics; Thermodynamics; Kramers rate theory; Nucleic acids; Solvent effects; Viscosity effects; Chemical kinetics; Quadruplex nucleic acids; DNA; Telomere

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APA (6th Edition):

Lannan, F. (2012). Folding of the human telomere sequence DNA in non-aqueous and otherwise viscous solvents. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/47598

Chicago Manual of Style (16th Edition):

Lannan, Ford. “Folding of the human telomere sequence DNA in non-aqueous and otherwise viscous solvents.” 2012. Masters Thesis, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/47598.

MLA Handbook (7th Edition):

Lannan, Ford. “Folding of the human telomere sequence DNA in non-aqueous and otherwise viscous solvents.” 2012. Web. 19 Jan 2021.

Vancouver:

Lannan F. Folding of the human telomere sequence DNA in non-aqueous and otherwise viscous solvents. [Internet] [Masters thesis]. Georgia Tech; 2012. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/47598.

Council of Science Editors:

Lannan F. Folding of the human telomere sequence DNA in non-aqueous and otherwise viscous solvents. [Masters Thesis]. Georgia Tech; 2012. Available from: http://hdl.handle.net/1853/47598

25. Roy, Poorna. Deconstructing the ribosome: specific interactions of a ribosomal RNA fragment with intact and fragmented L23 ribosomal protein.

Degree: MS, Chemistry and Biochemistry, 2013, Georgia Tech

 The complexity of translation is a classical dilemma in the evolution of biological systems. Efficient translation requires coordination of complex, highly evolved RNAs and proteins;… (more)

Subjects/Keywords: RNA; Ribosome; Yeast three-hybrid; Evolution; Nucleic acids; Gene expression

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APA (6th Edition):

Roy, P. (2013). Deconstructing the ribosome: specific interactions of a ribosomal RNA fragment with intact and fragmented L23 ribosomal protein. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/47579

Chicago Manual of Style (16th Edition):

Roy, Poorna. “Deconstructing the ribosome: specific interactions of a ribosomal RNA fragment with intact and fragmented L23 ribosomal protein.” 2013. Masters Thesis, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/47579.

MLA Handbook (7th Edition):

Roy, Poorna. “Deconstructing the ribosome: specific interactions of a ribosomal RNA fragment with intact and fragmented L23 ribosomal protein.” 2013. Web. 19 Jan 2021.

Vancouver:

Roy P. Deconstructing the ribosome: specific interactions of a ribosomal RNA fragment with intact and fragmented L23 ribosomal protein. [Internet] [Masters thesis]. Georgia Tech; 2013. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/47579.

Council of Science Editors:

Roy P. Deconstructing the ribosome: specific interactions of a ribosomal RNA fragment with intact and fragmented L23 ribosomal protein. [Masters Thesis]. Georgia Tech; 2013. Available from: http://hdl.handle.net/1853/47579

26. Canzoneri, Joshua Craig. Interaction of small molecules with nucleic acid targets: from RNA secondary structure to the riobosome.

Degree: PhD, Chemistry and Biochemistry, 2012, Georgia Tech

 Nucleic acids have proven to be viable targets for small molecule drugs. While many examples of such drugs are detailed in the literature, only a… (more)

Subjects/Keywords: Targeting nucleic acids; Rational drug design; Small molecule drugs; Nucleic acids; Gene expression; Genetic regulation; Drugs Design

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APA (6th Edition):

Canzoneri, J. C. (2012). Interaction of small molecules with nucleic acid targets: from RNA secondary structure to the riobosome. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/45769

Chicago Manual of Style (16th Edition):

Canzoneri, Joshua Craig. “Interaction of small molecules with nucleic acid targets: from RNA secondary structure to the riobosome.” 2012. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/45769.

MLA Handbook (7th Edition):

Canzoneri, Joshua Craig. “Interaction of small molecules with nucleic acid targets: from RNA secondary structure to the riobosome.” 2012. Web. 19 Jan 2021.

Vancouver:

Canzoneri JC. Interaction of small molecules with nucleic acid targets: from RNA secondary structure to the riobosome. [Internet] [Doctoral dissertation]. Georgia Tech; 2012. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/45769.

Council of Science Editors:

Canzoneri JC. Interaction of small molecules with nucleic acid targets: from RNA secondary structure to the riobosome. [Doctoral Dissertation]. Georgia Tech; 2012. Available from: http://hdl.handle.net/1853/45769

27. Engelhart, Aaron Edward. Nucleic acid assembly, polymerization, and ligand binding.

Degree: PhD, Chemistry and Biochemistry, 2012, Georgia Tech

 In the past 30 years, the discovery of capabilities of nucleic acids far beyond their well-known information-bearing capacity has profoundly influenced our understanding of these… (more)

Subjects/Keywords: Polymer; Cyclization; Dynamic covalent chemistry; Origin of life; RNA world; Reversible covalent bond; Template directed synthesis; Supramolecular chemistry; Chemistry, Physical and theoretical; Nucleic acids; Molecules; Ligand binding (Biochemistry)

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APA (6th Edition):

Engelhart, A. E. (2012). Nucleic acid assembly, polymerization, and ligand binding. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/45979

Chicago Manual of Style (16th Edition):

Engelhart, Aaron Edward. “Nucleic acid assembly, polymerization, and ligand binding.” 2012. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/45979.

MLA Handbook (7th Edition):

Engelhart, Aaron Edward. “Nucleic acid assembly, polymerization, and ligand binding.” 2012. Web. 19 Jan 2021.

Vancouver:

Engelhart AE. Nucleic acid assembly, polymerization, and ligand binding. [Internet] [Doctoral dissertation]. Georgia Tech; 2012. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/45979.

Council of Science Editors:

Engelhart AE. Nucleic acid assembly, polymerization, and ligand binding. [Doctoral Dissertation]. Georgia Tech; 2012. Available from: http://hdl.handle.net/1853/45979

28. Hsiao, Chiaolong. Computational bioinformatics on three-dimensional structures of ribosomes using multiresolutional analysis.

Degree: PhD, Chemistry and Biochemistry, 2008, Georgia Tech

 RNA is amazing. We found that without changing the backbone connectivity, RNA can maintain structural conservation in 3D via topology switches, at a single residue… (more)

Subjects/Keywords: Magnesium-binding motif; Superimposition; Structural alignment; Multiresolution; Ribosome; Tetraloop; Bioinformatics; Ribosomes; RNA; Image processing

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APA (6th Edition):

Hsiao, C. (2008). Computational bioinformatics on three-dimensional structures of ribosomes using multiresolutional analysis. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/26634

Chicago Manual of Style (16th Edition):

Hsiao, Chiaolong. “Computational bioinformatics on three-dimensional structures of ribosomes using multiresolutional analysis.” 2008. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/26634.

MLA Handbook (7th Edition):

Hsiao, Chiaolong. “Computational bioinformatics on three-dimensional structures of ribosomes using multiresolutional analysis.” 2008. Web. 19 Jan 2021.

Vancouver:

Hsiao C. Computational bioinformatics on three-dimensional structures of ribosomes using multiresolutional analysis. [Internet] [Doctoral dissertation]. Georgia Tech; 2008. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/26634.

Council of Science Editors:

Hsiao C. Computational bioinformatics on three-dimensional structures of ribosomes using multiresolutional analysis. [Doctoral Dissertation]. Georgia Tech; 2008. Available from: http://hdl.handle.net/1853/26634

29. Cannatelli, Mark Daniel. Exploiting the oxidizing capabilities of laccases for sustainable chemistry.

Degree: PhD, Chemistry and Biochemistry, 2017, Georgia Tech

 Enzyme catalyzed processes are rapidly becoming a viable means to accomplish chemical transformations in the field of synthetic chemistry. In an era where concern about… (more)

Subjects/Keywords: Green chemistry; Laccases; Lignin; Organic synthesis; Sustainability

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APA (6th Edition):

Cannatelli, M. D. (2017). Exploiting the oxidizing capabilities of laccases for sustainable chemistry. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58293

Chicago Manual of Style (16th Edition):

Cannatelli, Mark Daniel. “Exploiting the oxidizing capabilities of laccases for sustainable chemistry.” 2017. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/58293.

MLA Handbook (7th Edition):

Cannatelli, Mark Daniel. “Exploiting the oxidizing capabilities of laccases for sustainable chemistry.” 2017. Web. 19 Jan 2021.

Vancouver:

Cannatelli MD. Exploiting the oxidizing capabilities of laccases for sustainable chemistry. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/58293.

Council of Science Editors:

Cannatelli MD. Exploiting the oxidizing capabilities of laccases for sustainable chemistry. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/58293

30. Smeekens, Johanna. Novel mass spectrometry-based methods to identify and quantify extracellular glycoproteins.

Degree: PhD, Chemistry and Biochemistry, 2017, Georgia Tech

 Extracellular glycoproteins are extremely important to a variety of biological processes, including immune response, cell interactions and disease development. Despite their critical importance, glycoproteins are… (more)

Subjects/Keywords: Glycosylation; Proteomics; Mass spectrometry; Cell surface; Secretome

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APA (6th Edition):

Smeekens, J. (2017). Novel mass spectrometry-based methods to identify and quantify extracellular glycoproteins. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58297

Chicago Manual of Style (16th Edition):

Smeekens, Johanna. “Novel mass spectrometry-based methods to identify and quantify extracellular glycoproteins.” 2017. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/58297.

MLA Handbook (7th Edition):

Smeekens, Johanna. “Novel mass spectrometry-based methods to identify and quantify extracellular glycoproteins.” 2017. Web. 19 Jan 2021.

Vancouver:

Smeekens J. Novel mass spectrometry-based methods to identify and quantify extracellular glycoproteins. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/58297.

Council of Science Editors:

Smeekens J. Novel mass spectrometry-based methods to identify and quantify extracellular glycoproteins. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/58297

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