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You searched for +publisher:"Georgia Tech" +contributor:("Doyle, Donald"). Showing records 1 – 30 of 33 total matches.

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Georgia Tech

1. Peterson, Vincent. Progress towards the development of G-protein coupled receptor based logic gates.

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

 The yeast Saccharomyces cerevisiae along with the bacterium Escherichia coli have been popular model organisms for the creation or modification of chemical producing or chemical… (more)

Subjects/Keywords: Synthetic biology; GPCRs; Yeast; Cell signaling; Biosensors

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APA (6th Edition):

Peterson, V. (2016). Progress towards the development of G-protein coupled receptor based logic gates. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58141

Chicago Manual of Style (16th Edition):

Peterson, Vincent. “Progress towards the development of G-protein coupled receptor based logic gates.” 2016. Masters Thesis, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/58141.

MLA Handbook (7th Edition):

Peterson, Vincent. “Progress towards the development of G-protein coupled receptor based logic gates.” 2016. Web. 16 Jan 2021.

Vancouver:

Peterson V. Progress towards the development of G-protein coupled receptor based logic gates. [Internet] [Masters thesis]. Georgia Tech; 2016. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/58141.

Council of Science Editors:

Peterson V. Progress towards the development of G-protein coupled receptor based logic gates. [Masters Thesis]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/58141


Georgia Tech

2. Gong, He. Studies of genetic factors modulating polyglutamine toxicity in the yeast model.

Degree: PhD, Biology, 2011, Georgia Tech

 Polyglutamine-expanded fragments, derived from the human huntingtin protein, are aggregation-prone and toxic in yeast cells, bearing endogenous QN-rich proteins in the aggregated (prion) form. Attachment… (more)

Subjects/Keywords: Sup45; Sup35; Huntington disease; Arginine; Amyloid; Aggresome; Huntington's chorea; Genetic disorders

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APA (6th Edition):

Gong, H. (2011). Studies of genetic factors modulating polyglutamine toxicity in the yeast model. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/42796

Chicago Manual of Style (16th Edition):

Gong, He. “Studies of genetic factors modulating polyglutamine toxicity in the yeast model.” 2011. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/42796.

MLA Handbook (7th Edition):

Gong, He. “Studies of genetic factors modulating polyglutamine toxicity in the yeast model.” 2011. Web. 16 Jan 2021.

Vancouver:

Gong H. Studies of genetic factors modulating polyglutamine toxicity in the yeast model. [Internet] [Doctoral dissertation]. Georgia Tech; 2011. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/42796.

Council of Science Editors:

Gong H. Studies of genetic factors modulating polyglutamine toxicity in the yeast model. [Doctoral Dissertation]. Georgia Tech; 2011. Available from: http://hdl.handle.net/1853/42796

3. Haase, Nicholas Rudy. The development, characterization, and application of a biomimetic method of enzyme immobilization.

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

 This dissertation describes the characterization of layer-by-layer silica and titania coatings deposited using a protamine-induced method. It was found that silica coatings were thinner and… (more)

Subjects/Keywords: Enzyme immobilization; Functional coatings; Biomimetics; Biomimetics

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APA (6th Edition):

Haase, N. R. (2012). The development, characterization, and application of a biomimetic method of enzyme immobilization. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/45802

Chicago Manual of Style (16th Edition):

Haase, Nicholas Rudy. “The development, characterization, and application of a biomimetic method of enzyme immobilization.” 2012. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/45802.

MLA Handbook (7th Edition):

Haase, Nicholas Rudy. “The development, characterization, and application of a biomimetic method of enzyme immobilization.” 2012. Web. 16 Jan 2021.

Vancouver:

Haase NR. The development, characterization, and application of a biomimetic method of enzyme immobilization. [Internet] [Doctoral dissertation]. Georgia Tech; 2012. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/45802.

Council of Science Editors:

Haase NR. The development, characterization, and application of a biomimetic method of enzyme immobilization. [Doctoral Dissertation]. Georgia Tech; 2012. Available from: http://hdl.handle.net/1853/45802

4. Sims, Kacee Hall. Participation of de novo sphingolipid biosynthesis in the regulation of autophagy in response to diverse agents.

Degree: PhD, Chemistry and Biochemistry, 2011, Georgia Tech

 Sphingolipids are a complex family of molecules that participate in many aspects of cell structure and function, including an essential cellular process known as autophagy.… (more)

Subjects/Keywords: Sphingolipids; Mass spectrometry; Lipidomic; Autophagy; Fenretinide; Kdo2-lipid A; Biosynthesis; Cellular control mechanisms; Biological control systems

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APA (6th Edition):

Sims, K. H. (2011). Participation of de novo sphingolipid biosynthesis in the regulation of autophagy in response to diverse agents. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/42839

Chicago Manual of Style (16th Edition):

Sims, Kacee Hall. “Participation of de novo sphingolipid biosynthesis in the regulation of autophagy in response to diverse agents.” 2011. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/42839.

MLA Handbook (7th Edition):

Sims, Kacee Hall. “Participation of de novo sphingolipid biosynthesis in the regulation of autophagy in response to diverse agents.” 2011. Web. 16 Jan 2021.

Vancouver:

Sims KH. Participation of de novo sphingolipid biosynthesis in the regulation of autophagy in response to diverse agents. [Internet] [Doctoral dissertation]. Georgia Tech; 2011. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/42839.

Council of Science Editors:

Sims KH. Participation of de novo sphingolipid biosynthesis in the regulation of autophagy in response to diverse agents. [Doctoral Dissertation]. Georgia Tech; 2011. Available from: http://hdl.handle.net/1853/42839

5. 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 16, 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. 16 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 16]. 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

6. Persil Cetinkol, Ozgul. Small molecule recognition of homopurine nucleic acid structures.

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

 The thesis topic entitled above involves the use of small molecules as a general means to drive nucleic acid assembly and structural transitions. We have… (more)

Subjects/Keywords: Physical characterization; Nucleic acids; Small molecule binding; Assembly; Intercalation; Biomolecules; Nucleic acids; Supramolecular chemistry; Purines

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APA (6th Edition):

Persil Cetinkol, O. (2008). Small molecule recognition of homopurine nucleic acid structures. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/29739

Chicago Manual of Style (16th Edition):

Persil Cetinkol, Ozgul. “Small molecule recognition of homopurine nucleic acid structures.” 2008. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/29739.

MLA Handbook (7th Edition):

Persil Cetinkol, Ozgul. “Small molecule recognition of homopurine nucleic acid structures.” 2008. Web. 16 Jan 2021.

Vancouver:

Persil Cetinkol O. Small molecule recognition of homopurine nucleic acid structures. [Internet] [Doctoral dissertation]. Georgia Tech; 2008. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/29739.

Council of Science Editors:

Persil Cetinkol O. Small molecule recognition of homopurine nucleic acid structures. [Doctoral Dissertation]. Georgia Tech; 2008. Available from: http://hdl.handle.net/1853/29739

7. Chen, Buxin. Prion species barrier at the short phylogenetic distances in the yeast model.

Degree: PhD, Biology, 2008, Georgia Tech

 Prions are self-perpetuating and, in most cases, aggregation-prone protein isoforms that transmit neurodegenerative diseases in mammals and control heritable traits in yeast. Prion conversion requires… (more)

Subjects/Keywords: Species barrier; S. paradoxus; S. cerevisiae; Prion; S. bayanus; Prions; Prion diseases; Yeast; Communicable diseases

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APA (6th Edition):

Chen, B. (2008). Prion species barrier at the short phylogenetic distances in the yeast model. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/29762

Chicago Manual of Style (16th Edition):

Chen, Buxin. “Prion species barrier at the short phylogenetic distances in the yeast model.” 2008. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/29762.

MLA Handbook (7th Edition):

Chen, Buxin. “Prion species barrier at the short phylogenetic distances in the yeast model.” 2008. Web. 16 Jan 2021.

Vancouver:

Chen B. Prion species barrier at the short phylogenetic distances in the yeast model. [Internet] [Doctoral dissertation]. Georgia Tech; 2008. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/29762.

Council of Science Editors:

Chen B. Prion species barrier at the short phylogenetic distances in the yeast model. [Doctoral Dissertation]. Georgia Tech; 2008. Available from: http://hdl.handle.net/1853/29762

8. Ruffing, Anne M. Metabolic engineering and omics analysis of Agrobacterium sp. ATCC 31749 for oligosaccharide synthesis.

Degree: PhD, Chemical Engineering, 2010, Georgia Tech

 Oligosaccharides are important biomolecules that are targets and also components of many medical treatments, including treatments for cancer, HIV, and inflammation. While the demand for… (more)

Subjects/Keywords: Genome sequencing; Genomics; Transcriptomics; Oligosaccharide; Agrobacterium; Metabolic engineering; Oligosaccharide synthesis; Agrobacterium; Oligosaccharides Synthesis; Enzymes

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APA (6th Edition):

Ruffing, A. M. (2010). Metabolic engineering and omics analysis of Agrobacterium sp. ATCC 31749 for oligosaccharide synthesis. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/39507

Chicago Manual of Style (16th Edition):

Ruffing, Anne M. “Metabolic engineering and omics analysis of Agrobacterium sp. ATCC 31749 for oligosaccharide synthesis.” 2010. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/39507.

MLA Handbook (7th Edition):

Ruffing, Anne M. “Metabolic engineering and omics analysis of Agrobacterium sp. ATCC 31749 for oligosaccharide synthesis.” 2010. Web. 16 Jan 2021.

Vancouver:

Ruffing AM. Metabolic engineering and omics analysis of Agrobacterium sp. ATCC 31749 for oligosaccharide synthesis. [Internet] [Doctoral dissertation]. Georgia Tech; 2010. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/39507.

Council of Science Editors:

Ruffing AM. Metabolic engineering and omics analysis of Agrobacterium sp. ATCC 31749 for oligosaccharide synthesis. [Doctoral Dissertation]. Georgia Tech; 2010. Available from: http://hdl.handle.net/1853/39507

9. Lucrezi, Jacob. The evaluation of novel anti-inflammatory compounds in cell culture and experimental arthritis and identification of an inhibitor to early-stage loblolly pine somatic embryo growth.

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

 The interactions between the immune and nervous systems play an important role in immune and inflammatory conditions. Substance P (SP), the unidecapeptide RPKPQQFFGLM-NH2, is known… (more)

Subjects/Keywords: Substance P; TNF-alpha; p38 MAPK; JNK; RAW 264.7 macrophages; Loblolly pine; Somatic embryogenesis; Nanoparticle

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APA (6th Edition):

Lucrezi, J. (2013). The evaluation of novel anti-inflammatory compounds in cell culture and experimental arthritis and identification of an inhibitor to early-stage loblolly pine somatic embryo growth. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/52969

Chicago Manual of Style (16th Edition):

Lucrezi, Jacob. “The evaluation of novel anti-inflammatory compounds in cell culture and experimental arthritis and identification of an inhibitor to early-stage loblolly pine somatic embryo growth.” 2013. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/52969.

MLA Handbook (7th Edition):

Lucrezi, Jacob. “The evaluation of novel anti-inflammatory compounds in cell culture and experimental arthritis and identification of an inhibitor to early-stage loblolly pine somatic embryo growth.” 2013. Web. 16 Jan 2021.

Vancouver:

Lucrezi J. The evaluation of novel anti-inflammatory compounds in cell culture and experimental arthritis and identification of an inhibitor to early-stage loblolly pine somatic embryo growth. [Internet] [Doctoral dissertation]. Georgia Tech; 2013. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/52969.

Council of Science Editors:

Lucrezi J. The evaluation of novel anti-inflammatory compounds in cell culture and experimental arthritis and identification of an inhibitor to early-stage loblolly pine somatic embryo growth. [Doctoral Dissertation]. Georgia Tech; 2013. Available from: http://hdl.handle.net/1853/52969

10. Allegood, Jeremy Chadwick. Application of liquid chromatography tandem mass spectrometry for the separation and quantitative analysis of sphingolipids.

Degree: PhD, Chemistry and Biochemistry, 2011, Georgia Tech

 Sphingolipids are a highly diverse category of compounds that serve not only as components of biologic structures but also as regulators of numerous cell functions.… (more)

Subjects/Keywords: Sphingolipids; LC-MS/MS; Liquid chromatography; Chromatographic analysis; Tandem mass spectrometry

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APA (6th Edition):

Allegood, J. C. (2011). Application of liquid chromatography tandem mass spectrometry for the separation and quantitative analysis of sphingolipids. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/42691

Chicago Manual of Style (16th Edition):

Allegood, Jeremy Chadwick. “Application of liquid chromatography tandem mass spectrometry for the separation and quantitative analysis of sphingolipids.” 2011. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/42691.

MLA Handbook (7th Edition):

Allegood, Jeremy Chadwick. “Application of liquid chromatography tandem mass spectrometry for the separation and quantitative analysis of sphingolipids.” 2011. Web. 16 Jan 2021.

Vancouver:

Allegood JC. Application of liquid chromatography tandem mass spectrometry for the separation and quantitative analysis of sphingolipids. [Internet] [Doctoral dissertation]. Georgia Tech; 2011. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/42691.

Council of Science Editors:

Allegood JC. Application of liquid chromatography tandem mass spectrometry for the separation and quantitative analysis of sphingolipids. [Doctoral Dissertation]. Georgia Tech; 2011. Available from: http://hdl.handle.net/1853/42691

11. Cowan, Elizabeth Alice. An investigation of the therapeutic potential of phenylaminoalkyl selenides through mechanistic and biological studies and an exploration of ciber: the center of innovative biomaterial education and research.

Degree: PhD, Chemistry and Biochemistry, 2011, Georgia Tech

 The overproduction of reactive oxygen species (ROS) have been linked to diseases and other pathologies. As therapeutic agents, antioxidants have been tested and some shown… (more)

Subjects/Keywords: Thioselenurane; Stopped-flow; Antioxidant; Phenlyaminoalkyl selenides; Antioxidants; Selenium; Active oxygen; Cancer; Cancer Treatment

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APA (6th Edition):

Cowan, E. A. (2011). An investigation of the therapeutic potential of phenylaminoalkyl selenides through mechanistic and biological studies and an exploration of ciber: the center of innovative biomaterial education and research. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/42937

Chicago Manual of Style (16th Edition):

Cowan, Elizabeth Alice. “An investigation of the therapeutic potential of phenylaminoalkyl selenides through mechanistic and biological studies and an exploration of ciber: the center of innovative biomaterial education and research.” 2011. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/42937.

MLA Handbook (7th Edition):

Cowan, Elizabeth Alice. “An investigation of the therapeutic potential of phenylaminoalkyl selenides through mechanistic and biological studies and an exploration of ciber: the center of innovative biomaterial education and research.” 2011. Web. 16 Jan 2021.

Vancouver:

Cowan EA. An investigation of the therapeutic potential of phenylaminoalkyl selenides through mechanistic and biological studies and an exploration of ciber: the center of innovative biomaterial education and research. [Internet] [Doctoral dissertation]. Georgia Tech; 2011. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/42937.

Council of Science Editors:

Cowan EA. An investigation of the therapeutic potential of phenylaminoalkyl selenides through mechanistic and biological studies and an exploration of ciber: the center of innovative biomaterial education and research. [Doctoral Dissertation]. Georgia Tech; 2011. Available from: http://hdl.handle.net/1853/42937

12. Johnson, Kenyetta Alicia. Extending chemical complemenation to bacteria and furthering nuclear receptor based protein engineering and drug discovery.

Degree: PhD, Chemistry and Biochemistry, 2009, Georgia Tech

 Nuclear receptors (NRs) are modular ligand-activated transcription factors that control a broad range of physiological processes by regulating the expression of essential genes involved in… (more)

Subjects/Keywords: Protein engineering; Nuclear receptor; Chemical complementation; Drug discovery; Nuclear receptors (Biochemistry); Developmental pharmacology; Protein engineering; Yeast Genetics

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APA (6th Edition):

Johnson, K. A. (2009). Extending chemical complemenation to bacteria and furthering nuclear receptor based protein engineering and drug discovery. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/29652

Chicago Manual of Style (16th Edition):

Johnson, Kenyetta Alicia. “Extending chemical complemenation to bacteria and furthering nuclear receptor based protein engineering and drug discovery.” 2009. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/29652.

MLA Handbook (7th Edition):

Johnson, Kenyetta Alicia. “Extending chemical complemenation to bacteria and furthering nuclear receptor based protein engineering and drug discovery.” 2009. Web. 16 Jan 2021.

Vancouver:

Johnson KA. Extending chemical complemenation to bacteria and furthering nuclear receptor based protein engineering and drug discovery. [Internet] [Doctoral dissertation]. Georgia Tech; 2009. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/29652.

Council of Science Editors:

Johnson KA. Extending chemical complemenation to bacteria and furthering nuclear receptor based protein engineering and drug discovery. [Doctoral Dissertation]. Georgia Tech; 2009. Available from: http://hdl.handle.net/1853/29652

13. Bender, Shana Lynn. A study of protein dynamics and cofactor interactions in Photosystem I.

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

 Previous research has underscored the importance of protein dynamics during light-induced electron transfer; however, specific interactions have not been well characterized. It is of particular… (more)

Subjects/Keywords: FT-IR spectroscopy; Photosysystem I; Protein dynamics; Electron transfer; Charge exchange; Photosynthesis; Proteins Structure-activity relationships

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APA (6th Edition):

Bender, S. L. (2008). A study of protein dynamics and cofactor interactions in Photosystem I. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/26463

Chicago Manual of Style (16th Edition):

Bender, Shana Lynn. “A study of protein dynamics and cofactor interactions in Photosystem I.” 2008. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/26463.

MLA Handbook (7th Edition):

Bender, Shana Lynn. “A study of protein dynamics and cofactor interactions in Photosystem I.” 2008. Web. 16 Jan 2021.

Vancouver:

Bender SL. A study of protein dynamics and cofactor interactions in Photosystem I. [Internet] [Doctoral dissertation]. Georgia Tech; 2008. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/26463.

Council of Science Editors:

Bender SL. A study of protein dynamics and cofactor interactions in Photosystem I. [Doctoral Dissertation]. Georgia Tech; 2008. Available from: http://hdl.handle.net/1853/26463

14. Castillo, Hilda S. Mutational analysis and engineering of the human vitamin D receptor to bind and activate in response to a novel small molecule ligand.

Degree: PhD, Chemistry and Biochemistry, 2011, Georgia Tech

 Nuclear receptors (NRs) are ligand-activated transcription factors that regulate the expression of genes involved in all physiological activities. Disruption in NR function (e.g. mutations) can… (more)

Subjects/Keywords: Mutagenesis; Protein engineering; Nuclear receptor; Vitamin D receptor; Lithocholic acid; Cholecalciferol; Ligands (Biochemistry); Vitamin D in the body; Nuclear receptors (Biochemistry)

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APA (6th Edition):

Castillo, H. S. (2011). Mutational analysis and engineering of the human vitamin D receptor to bind and activate in response to a novel small molecule ligand. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/39502

Chicago Manual of Style (16th Edition):

Castillo, Hilda S. “Mutational analysis and engineering of the human vitamin D receptor to bind and activate in response to a novel small molecule ligand.” 2011. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/39502.

MLA Handbook (7th Edition):

Castillo, Hilda S. “Mutational analysis and engineering of the human vitamin D receptor to bind and activate in response to a novel small molecule ligand.” 2011. Web. 16 Jan 2021.

Vancouver:

Castillo HS. Mutational analysis and engineering of the human vitamin D receptor to bind and activate in response to a novel small molecule ligand. [Internet] [Doctoral dissertation]. Georgia Tech; 2011. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/39502.

Council of Science Editors:

Castillo HS. Mutational analysis and engineering of the human vitamin D receptor to bind and activate in response to a novel small molecule ligand. [Doctoral Dissertation]. Georgia Tech; 2011. Available from: http://hdl.handle.net/1853/39502

15. Ousley, Amanda. Engineering the human vitamin D receptor to bind a novel small molecule: investigating the structure-function relationship between human vitamin d receptor and various ligands.

Degree: PhD, Chemistry and Biochemistry, 2011, Georgia Tech

 The human vitamin D receptor (hVDR) is a member of the nuclear receptor superfamily, involved in calcium and phosphate homeostasis; hence implicated in a number… (more)

Subjects/Keywords: Lithocholic acid; Cholecalciferol; Human vitamin D receptor; Nuclear receptors; Vitamin D in the body; Protein engineering; Ligand binding (Biochemistry); Receptor complexes (Biochemistry); Mutagenesis

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APA (6th Edition):

Ousley, A. (2011). Engineering the human vitamin D receptor to bind a novel small molecule: investigating the structure-function relationship between human vitamin d receptor and various ligands. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/39580

Chicago Manual of Style (16th Edition):

Ousley, Amanda. “Engineering the human vitamin D receptor to bind a novel small molecule: investigating the structure-function relationship between human vitamin d receptor and various ligands.” 2011. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/39580.

MLA Handbook (7th Edition):

Ousley, Amanda. “Engineering the human vitamin D receptor to bind a novel small molecule: investigating the structure-function relationship between human vitamin d receptor and various ligands.” 2011. Web. 16 Jan 2021.

Vancouver:

Ousley A. Engineering the human vitamin D receptor to bind a novel small molecule: investigating the structure-function relationship between human vitamin d receptor and various ligands. [Internet] [Doctoral dissertation]. Georgia Tech; 2011. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/39580.

Council of Science Editors:

Ousley A. Engineering the human vitamin D receptor to bind a novel small molecule: investigating the structure-function relationship between human vitamin d receptor and various ligands. [Doctoral Dissertation]. Georgia Tech; 2011. Available from: http://hdl.handle.net/1853/39580

16. Taylor, Jennifer. Engineering and improving a molecular switch system for gene therapy applications.

Degree: PhD, Chemistry and Biochemistry, 2011, Georgia Tech

 Molecular switch systems that activate gene expression by a small molecule are effective technologies that are widely used in applied biological research. Previously, two orthogonal… (more)

Subjects/Keywords: Protein engineering; Gene therapy; Molecular switch systems; Gene regulation systems; RXR; Nuclear receptors; Gene therapy; Nuclear receptors (Biochemistry); Ligands (Biochemistry)

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APA (6th Edition):

Taylor, J. (2011). Engineering and improving a molecular switch system for gene therapy applications. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/39501

Chicago Manual of Style (16th Edition):

Taylor, Jennifer. “Engineering and improving a molecular switch system for gene therapy applications.” 2011. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/39501.

MLA Handbook (7th Edition):

Taylor, Jennifer. “Engineering and improving a molecular switch system for gene therapy applications.” 2011. Web. 16 Jan 2021.

Vancouver:

Taylor J. Engineering and improving a molecular switch system for gene therapy applications. [Internet] [Doctoral dissertation]. Georgia Tech; 2011. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/39501.

Council of Science Editors:

Taylor J. Engineering and improving a molecular switch system for gene therapy applications. [Doctoral Dissertation]. Georgia Tech; 2011. Available from: http://hdl.handle.net/1853/39501


Georgia Tech

17. Moulaei, Tinoush. Interaction of B-DNA and Monovalent Cations: Theory and Practice in X-Ray Crystallography.

Degree: PhD, Chemistry and Biochemistry, 2004, Georgia Tech

 In this thesis, fundamental questions about the nature of the solvent/counter-ion region of x-ray crystal structures are raised. The ambiguity in the identity and occupancy… (more)

Subjects/Keywords: Anomalous scattering; Nucleic acids; DNA; Rubidium; Thallium; X-ray crystallography; Thallium; Rubidium; Monovalent cations; DNA

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APA (6th Edition):

Moulaei, T. (2004). Interaction of B-DNA and Monovalent Cations: Theory and Practice in X-Ray Crystallography. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/4927

Chicago Manual of Style (16th Edition):

Moulaei, Tinoush. “Interaction of B-DNA and Monovalent Cations: Theory and Practice in X-Ray Crystallography.” 2004. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/4927.

MLA Handbook (7th Edition):

Moulaei, Tinoush. “Interaction of B-DNA and Monovalent Cations: Theory and Practice in X-Ray Crystallography.” 2004. Web. 16 Jan 2021.

Vancouver:

Moulaei T. Interaction of B-DNA and Monovalent Cations: Theory and Practice in X-Ray Crystallography. [Internet] [Doctoral dissertation]. Georgia Tech; 2004. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/4927.

Council of Science Editors:

Moulaei T. Interaction of B-DNA and Monovalent Cations: Theory and Practice in X-Ray Crystallography. [Doctoral Dissertation]. Georgia Tech; 2004. Available from: http://hdl.handle.net/1853/4927


Georgia Tech

18. Banna, Christopher David. Characterization of DAP1/YPL170W: the Saccharomyces cerevisiae Membrane Associated Progesterone Receptor (MAPR)Homologue.

Degree: PhD, Biology, 2005, Georgia Tech

 Characterization of DAP1/YPL170W: the Saccharomyces cerevisiae Membrane Associated Progesterone Receptor (MAPR) Homologue Christopher D. Banna 135 pages Directed by Dr. Jung H. Choi MAPRs (Membrane… (more)

Subjects/Keywords: Yeast; MAPR; DAP1; Sterol

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APA (6th Edition):

Banna, C. D. (2005). Characterization of DAP1/YPL170W: the Saccharomyces cerevisiae Membrane Associated Progesterone Receptor (MAPR)Homologue. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/6826

Chicago Manual of Style (16th Edition):

Banna, Christopher David. “Characterization of DAP1/YPL170W: the Saccharomyces cerevisiae Membrane Associated Progesterone Receptor (MAPR)Homologue.” 2005. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/6826.

MLA Handbook (7th Edition):

Banna, Christopher David. “Characterization of DAP1/YPL170W: the Saccharomyces cerevisiae Membrane Associated Progesterone Receptor (MAPR)Homologue.” 2005. Web. 16 Jan 2021.

Vancouver:

Banna CD. Characterization of DAP1/YPL170W: the Saccharomyces cerevisiae Membrane Associated Progesterone Receptor (MAPR)Homologue. [Internet] [Doctoral dissertation]. Georgia Tech; 2005. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/6826.

Council of Science Editors:

Banna CD. Characterization of DAP1/YPL170W: the Saccharomyces cerevisiae Membrane Associated Progesterone Receptor (MAPR)Homologue. [Doctoral Dissertation]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/6826


Georgia Tech

19. Sasine, Joshua Sidney. Nanocapsules: Calix[4]arene Derivatives that Self-Assemble through Ionic Interactions in Polar Solvents.

Degree: PhD, Chemistry and Biochemistry, 2005, Georgia Tech

 Molecular capsules consist of two or more molecules that bind through either covalent or noncovalent interactions to form a structure with an internal void capable… (more)

Subjects/Keywords: Calix[4]arene; Nanocapsule; Polar; Ionic; Association; Dimers; Self-assembly; Nanostructured materials; Calixarenes; Drugs Physiological transport Research Methodology

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APA (6th Edition):

Sasine, J. S. (2005). Nanocapsules: Calix[4]arene Derivatives that Self-Assemble through Ionic Interactions in Polar Solvents. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/6888

Chicago Manual of Style (16th Edition):

Sasine, Joshua Sidney. “Nanocapsules: Calix[4]arene Derivatives that Self-Assemble through Ionic Interactions in Polar Solvents.” 2005. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/6888.

MLA Handbook (7th Edition):

Sasine, Joshua Sidney. “Nanocapsules: Calix[4]arene Derivatives that Self-Assemble through Ionic Interactions in Polar Solvents.” 2005. Web. 16 Jan 2021.

Vancouver:

Sasine JS. Nanocapsules: Calix[4]arene Derivatives that Self-Assemble through Ionic Interactions in Polar Solvents. [Internet] [Doctoral dissertation]. Georgia Tech; 2005. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/6888.

Council of Science Editors:

Sasine JS. Nanocapsules: Calix[4]arene Derivatives that Self-Assemble through Ionic Interactions in Polar Solvents. [Doctoral Dissertation]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/6888


Georgia Tech

20. Campbell, Amy. Design, Synthesis, and Evaluation of Cysteine Protease Inhibitors.

Degree: PhD, Chemistry and Biochemistry, 2005, Georgia Tech

 Both clan CA and clan CD proteases have a variety of physiological and pathological roles. In particular, both clans have members who have been implicated… (more)

Subjects/Keywords: Epoxysuccinyl aza-peptides; Molecular modeling; Caspases; Irreversible kinetics; Aza-peptide epoxides

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APA (6th Edition):

Campbell, A. (2005). Design, Synthesis, and Evaluation of Cysteine Protease Inhibitors. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/14046

Chicago Manual of Style (16th Edition):

Campbell, Amy. “Design, Synthesis, and Evaluation of Cysteine Protease Inhibitors.” 2005. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/14046.

MLA Handbook (7th Edition):

Campbell, Amy. “Design, Synthesis, and Evaluation of Cysteine Protease Inhibitors.” 2005. Web. 16 Jan 2021.

Vancouver:

Campbell A. Design, Synthesis, and Evaluation of Cysteine Protease Inhibitors. [Internet] [Doctoral dissertation]. Georgia Tech; 2005. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/14046.

Council of Science Editors:

Campbell A. Design, Synthesis, and Evaluation of Cysteine Protease Inhibitors. [Doctoral Dissertation]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/14046


Georgia Tech

21. Ghosh, Avik Kumar. Charge migration and one-electron oxidation at adenine and thymidine containing DNA strands and role of guanine N1 imino proton in long range charge migration through DNA.

Degree: PhD, Chemistry and Biochemistry, 2007, Georgia Tech

 DNA is the carrier of biological information and damage to DNA has been believed to be responsible for many diseases including aging and cancer. One… (more)

Subjects/Keywords: DNA; Charge migration; Oxidative damage

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APA (6th Edition):

Ghosh, A. K. (2007). Charge migration and one-electron oxidation at adenine and thymidine containing DNA strands and role of guanine N1 imino proton in long range charge migration through DNA. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/16203

Chicago Manual of Style (16th Edition):

Ghosh, Avik Kumar. “Charge migration and one-electron oxidation at adenine and thymidine containing DNA strands and role of guanine N1 imino proton in long range charge migration through DNA.” 2007. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/16203.

MLA Handbook (7th Edition):

Ghosh, Avik Kumar. “Charge migration and one-electron oxidation at adenine and thymidine containing DNA strands and role of guanine N1 imino proton in long range charge migration through DNA.” 2007. Web. 16 Jan 2021.

Vancouver:

Ghosh AK. Charge migration and one-electron oxidation at adenine and thymidine containing DNA strands and role of guanine N1 imino proton in long range charge migration through DNA. [Internet] [Doctoral dissertation]. Georgia Tech; 2007. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/16203.

Council of Science Editors:

Ghosh AK. Charge migration and one-electron oxidation at adenine and thymidine containing DNA strands and role of guanine N1 imino proton in long range charge migration through DNA. [Doctoral Dissertation]. Georgia Tech; 2007. Available from: http://hdl.handle.net/1853/16203


Georgia Tech

22. Kulis, Michael D., Jr. Islet Neogenesis Associated Protein-Related Protein: From Gene to Folded Protein.

Degree: PhD, Chemistry and Biochemistry, 2006, Georgia Tech

 Type 1 diabetes is the direct result of an autoimmune attack on the pancreatic islet cells. The islets contain b cells, which are the only… (more)

Subjects/Keywords: Islet; Regeneration; Diabetes; Islet Neogenesis Associated Protein; Pancreas; Molecular biology; Protein purification; Protein folding; NMR; HSQC; CD

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APA (6th Edition):

Kulis, Michael D., J. (2006). Islet Neogenesis Associated Protein-Related Protein: From Gene to Folded Protein. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/10436

Chicago Manual of Style (16th Edition):

Kulis, Michael D., Jr. “Islet Neogenesis Associated Protein-Related Protein: From Gene to Folded Protein.” 2006. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/10436.

MLA Handbook (7th Edition):

Kulis, Michael D., Jr. “Islet Neogenesis Associated Protein-Related Protein: From Gene to Folded Protein.” 2006. Web. 16 Jan 2021.

Vancouver:

Kulis, Michael D. J. Islet Neogenesis Associated Protein-Related Protein: From Gene to Folded Protein. [Internet] [Doctoral dissertation]. Georgia Tech; 2006. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/10436.

Council of Science Editors:

Kulis, Michael D. J. Islet Neogenesis Associated Protein-Related Protein: From Gene to Folded Protein. [Doctoral Dissertation]. Georgia Tech; 2006. Available from: http://hdl.handle.net/1853/10436


Georgia Tech

23. Jain, Swapan Satyen. Nucleic Acid Assembly Using Small Molecule Interactions.

Degree: PhD, Chemistry and Biochemistry, 2006, Georgia Tech

 Lifes origin is, in many ways, coupled to understanding the evolution of nucleic acids. In contemporary life, proteins and nucleic acids are intricately dependent upon… (more)

Subjects/Keywords: Proflavine; Assembly; Coralyne; Intercalation; Molecular midwife hypothesis; Nucleic acids; Ligation

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APA (6th Edition):

Jain, S. S. (2006). Nucleic Acid Assembly Using Small Molecule Interactions. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/11596

Chicago Manual of Style (16th Edition):

Jain, Swapan Satyen. “Nucleic Acid Assembly Using Small Molecule Interactions.” 2006. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/11596.

MLA Handbook (7th Edition):

Jain, Swapan Satyen. “Nucleic Acid Assembly Using Small Molecule Interactions.” 2006. Web. 16 Jan 2021.

Vancouver:

Jain SS. Nucleic Acid Assembly Using Small Molecule Interactions. [Internet] [Doctoral dissertation]. Georgia Tech; 2006. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/11596.

Council of Science Editors:

Jain SS. Nucleic Acid Assembly Using Small Molecule Interactions. [Doctoral Dissertation]. Georgia Tech; 2006. Available from: http://hdl.handle.net/1853/11596


Georgia Tech

24. Onyemauwa, Frank Okezie. Investigation of the Role of Groove Hydration and Charged Nucleosides in DNA Charge Transfer.

Degree: PhD, Chemistry and Biochemistry, 2006, Georgia Tech

 Structural analyses of DNA oligonucleotides indicate the presence of bound water molecules in the major and minor grooves of DNA. These water molecules participate in… (more)

Subjects/Keywords: DNA oxidation; Synthesis of pyridinium nucleoside; Charged nucleosides; DNA charge transfer; Nucleosides; Nucleosynthesis; DNA Synthesis

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APA (6th Edition):

Onyemauwa, F. O. (2006). Investigation of the Role of Groove Hydration and Charged Nucleosides in DNA Charge Transfer. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/11634

Chicago Manual of Style (16th Edition):

Onyemauwa, Frank Okezie. “Investigation of the Role of Groove Hydration and Charged Nucleosides in DNA Charge Transfer.” 2006. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/11634.

MLA Handbook (7th Edition):

Onyemauwa, Frank Okezie. “Investigation of the Role of Groove Hydration and Charged Nucleosides in DNA Charge Transfer.” 2006. Web. 16 Jan 2021.

Vancouver:

Onyemauwa FO. Investigation of the Role of Groove Hydration and Charged Nucleosides in DNA Charge Transfer. [Internet] [Doctoral dissertation]. Georgia Tech; 2006. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/11634.

Council of Science Editors:

Onyemauwa FO. Investigation of the Role of Groove Hydration and Charged Nucleosides in DNA Charge Transfer. [Doctoral Dissertation]. Georgia Tech; 2006. Available from: http://hdl.handle.net/1853/11634


Georgia Tech

25. Schwimmer, Lauren J. Engineering ligand-receptor pairs for small molecule control of transcription.

Degree: PhD, Chemistry and Biochemistry, 2005, Georgia Tech

 Creating receptors for control of transcription with arbitrary small molecules has widespread applications including gene therapy, biosensors, and enzyme engineering. Using the combination of high… (more)

Subjects/Keywords: Chemical complementation; Ligand-receptor pair; Protein engineering; Retinoid X receptor; Nuclear receptor; Codon randomized libraries; Transcription factors; Protein engineering; Nuclear receptors (Biochemistry); Genetic engineering

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APA (6th Edition):

Schwimmer, L. J. (2005). Engineering ligand-receptor pairs for small molecule control of transcription. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/11651

Chicago Manual of Style (16th Edition):

Schwimmer, Lauren J. “Engineering ligand-receptor pairs for small molecule control of transcription.” 2005. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/11651.

MLA Handbook (7th Edition):

Schwimmer, Lauren J. “Engineering ligand-receptor pairs for small molecule control of transcription.” 2005. Web. 16 Jan 2021.

Vancouver:

Schwimmer LJ. Engineering ligand-receptor pairs for small molecule control of transcription. [Internet] [Doctoral dissertation]. Georgia Tech; 2005. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/11651.

Council of Science Editors:

Schwimmer LJ. Engineering ligand-receptor pairs for small molecule control of transcription. [Doctoral Dissertation]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/11651


Georgia Tech

26. Bridges, Sylvia Shadinger. Design, synthesis, and evaluation of cysteine protease inhibitors.

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

 Proteases are enzymes that cleave protein amide bonds. Proteases are involved in a myriad of biological processes and are considered good targets for drug design.… (more)

Subjects/Keywords: Clostripain; Proteinase; Cysteine proteinases Inhibitors

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APA (6th Edition):

Bridges, S. S. (2008). Design, synthesis, and evaluation of cysteine protease inhibitors. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/29738

Chicago Manual of Style (16th Edition):

Bridges, Sylvia Shadinger. “Design, synthesis, and evaluation of cysteine protease inhibitors.” 2008. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/29738.

MLA Handbook (7th Edition):

Bridges, Sylvia Shadinger. “Design, synthesis, and evaluation of cysteine protease inhibitors.” 2008. Web. 16 Jan 2021.

Vancouver:

Bridges SS. Design, synthesis, and evaluation of cysteine protease inhibitors. [Internet] [Doctoral dissertation]. Georgia Tech; 2008. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/29738.

Council of Science Editors:

Bridges SS. Design, synthesis, and evaluation of cysteine protease inhibitors. [Doctoral Dissertation]. Georgia Tech; 2008. Available from: http://hdl.handle.net/1853/29738


Georgia Tech

27. Watt, Terry J. Engineering a better receptor: characterization of retinoid x receptor alpha and functional variants.

Degree: PhD, Chemistry and Biochemistry, 2007, Georgia Tech

 The human retinoid X receptor alpha (hRXRalpha) is a member of the nuclear receptor super-family of ligand-activated transcription factors. The Doyle laboratory has previously engineered… (more)

Subjects/Keywords: Ligand binding; Protein engineering; Oligomerization; Thermal denaturation; Retinoid X receptor; Retinoids; Nuclear receptors (Biochemistry); Ligand binding (Biochemistry); DNA

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APA (6th Edition):

Watt, T. J. (2007). Engineering a better receptor: characterization of retinoid x receptor alpha and functional variants. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/26647

Chicago Manual of Style (16th Edition):

Watt, Terry J. “Engineering a better receptor: characterization of retinoid x receptor alpha and functional variants.” 2007. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/26647.

MLA Handbook (7th Edition):

Watt, Terry J. “Engineering a better receptor: characterization of retinoid x receptor alpha and functional variants.” 2007. Web. 16 Jan 2021.

Vancouver:

Watt TJ. Engineering a better receptor: characterization of retinoid x receptor alpha and functional variants. [Internet] [Doctoral dissertation]. Georgia Tech; 2007. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/26647.

Council of Science Editors:

Watt TJ. Engineering a better receptor: characterization of retinoid x receptor alpha and functional variants. [Doctoral Dissertation]. Georgia Tech; 2007. Available from: http://hdl.handle.net/1853/26647


Georgia Tech

28. Bariar, Bhawana. Effects of the components of the Get pathway on prion propagation.

Degree: MS, Biology, 2007, Georgia Tech

 Yeast prions e.g. [PSI+], [PIN+] and [URE3] are similar to mammalian amyloids that cause neurodegenerative diseases. [PSI+] is the aggregated self-perpetuating (prion) isoform of Sup35,… (more)

Subjects/Keywords: Get complex; Hsp104; Prion; [PSI+]; Yeast; Get3; Get1; Get2; Prions; Yeast

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APA (6th Edition):

Bariar, B. (2007). Effects of the components of the Get pathway on prion propagation. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/26659

Chicago Manual of Style (16th Edition):

Bariar, Bhawana. “Effects of the components of the Get pathway on prion propagation.” 2007. Masters Thesis, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/26659.

MLA Handbook (7th Edition):

Bariar, Bhawana. “Effects of the components of the Get pathway on prion propagation.” 2007. Web. 16 Jan 2021.

Vancouver:

Bariar B. Effects of the components of the Get pathway on prion propagation. [Internet] [Masters thesis]. Georgia Tech; 2007. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/26659.

Council of Science Editors:

Bariar B. Effects of the components of the Get pathway on prion propagation. [Masters Thesis]. Georgia Tech; 2007. Available from: http://hdl.handle.net/1853/26659


Georgia Tech

29. Wu, Yonggang. Design, Synthesis and Characterization of Zinc(II)-Selective Ratiometric Fluorescent Sensors.

Degree: PhD, Chemistry and Biochemistry, 2007, Georgia Tech

 Zinc is an important micronutrient but the biological function of its labile form is poorly understood. Zinc selective fluorescence sensors, recognized as the major tool… (more)

Subjects/Keywords: Zinc; Fluorescent sensors; Fluorescent probes; Biosensors; Zinc

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APA (6th Edition):

Wu, Y. (2007). Design, Synthesis and Characterization of Zinc(II)-Selective Ratiometric Fluorescent Sensors. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/19735

Chicago Manual of Style (16th Edition):

Wu, Yonggang. “Design, Synthesis and Characterization of Zinc(II)-Selective Ratiometric Fluorescent Sensors.” 2007. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/19735.

MLA Handbook (7th Edition):

Wu, Yonggang. “Design, Synthesis and Characterization of Zinc(II)-Selective Ratiometric Fluorescent Sensors.” 2007. Web. 16 Jan 2021.

Vancouver:

Wu Y. Design, Synthesis and Characterization of Zinc(II)-Selective Ratiometric Fluorescent Sensors. [Internet] [Doctoral dissertation]. Georgia Tech; 2007. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/19735.

Council of Science Editors:

Wu Y. Design, Synthesis and Characterization of Zinc(II)-Selective Ratiometric Fluorescent Sensors. [Doctoral Dissertation]. Georgia Tech; 2007. Available from: http://hdl.handle.net/1853/19735


Georgia Tech

30. O'Daniel, Peter Ivo. Exploring structural diversity in nucleoside and nucleic acid drug design.

Degree: PhD, Chemistry and Biochemistry, 2005, Georgia Tech

 The design and optimization of chemotherapeutic molecules through molecular modeling is a rapidly growing aspect of drug design. The recent increase in computer power and… (more)

Subjects/Keywords: DNA; Nucleosides; Nucleotides; Enzymes; Fleximers; Drugs Design

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APA (6th Edition):

O'Daniel, P. I. (2005). Exploring structural diversity in nucleoside and nucleic acid drug design. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/14042

Chicago Manual of Style (16th Edition):

O'Daniel, Peter Ivo. “Exploring structural diversity in nucleoside and nucleic acid drug design.” 2005. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/14042.

MLA Handbook (7th Edition):

O'Daniel, Peter Ivo. “Exploring structural diversity in nucleoside and nucleic acid drug design.” 2005. Web. 16 Jan 2021.

Vancouver:

O'Daniel PI. Exploring structural diversity in nucleoside and nucleic acid drug design. [Internet] [Doctoral dissertation]. Georgia Tech; 2005. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/14042.

Council of Science Editors:

O'Daniel PI. Exploring structural diversity in nucleoside and nucleic acid drug design. [Doctoral Dissertation]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/14042

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