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You searched for +publisher:"Georgia Tech" +contributor:("Oyelere, Adegboyega"). Showing records 1 – 30 of 53 total matches.

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1. 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 17, 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. 17 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 17]. 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

2. Snare, David Joseph. Mechanistic evaluation of red algal extracts that slow aging.

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

 Aging results from an accumulation of damage to macromolecules inhibiting cellular replication, repair, and other necessary functions. Damage may be due to environmental stressors such… (more)

Subjects/Keywords: Aging; Red algae; Red algae; Aging Prevention; Rotifera

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APA (6th Edition):

Snare, D. J. (2013). Mechanistic evaluation of red algal extracts that slow aging. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/49050

Chicago Manual of Style (16th Edition):

Snare, David Joseph. “Mechanistic evaluation of red algal extracts that slow aging.” 2013. Masters Thesis, Georgia Tech. Accessed January 17, 2021. http://hdl.handle.net/1853/49050.

MLA Handbook (7th Edition):

Snare, David Joseph. “Mechanistic evaluation of red algal extracts that slow aging.” 2013. Web. 17 Jan 2021.

Vancouver:

Snare DJ. Mechanistic evaluation of red algal extracts that slow aging. [Internet] [Masters thesis]. Georgia Tech; 2013. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1853/49050.

Council of Science Editors:

Snare DJ. Mechanistic evaluation of red algal extracts that slow aging. [Masters Thesis]. Georgia Tech; 2013. Available from: http://hdl.handle.net/1853/49050


Georgia Tech

3. Ingram, Rena. Label-free bioanalytical methods for investigating bimolecular interactions: A review.

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

 Interactions between biological molecules such as DNA, RNA, protein, lipids, and carbohydrates are critical to the understanding of all biological, physical, and chemical processes such… (more)

Subjects/Keywords: Label-free; Label-required; Isothermal titration calorimetry; Surface plasmon resonance; Backscattering interferometry; Bio-layer interferometry; Field-effect transistor-based biosensors; Magnetoelastic biosensors; Biophotonic biosensors

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APA (6th Edition):

Ingram, R. (2017). Label-free bioanalytical methods for investigating bimolecular interactions: A review. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/62606

Chicago Manual of Style (16th Edition):

Ingram, Rena. “Label-free bioanalytical methods for investigating bimolecular interactions: A review.” 2017. Masters Thesis, Georgia Tech. Accessed January 17, 2021. http://hdl.handle.net/1853/62606.

MLA Handbook (7th Edition):

Ingram, Rena. “Label-free bioanalytical methods for investigating bimolecular interactions: A review.” 2017. Web. 17 Jan 2021.

Vancouver:

Ingram R. Label-free bioanalytical methods for investigating bimolecular interactions: A review. [Internet] [Masters thesis]. Georgia Tech; 2017. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1853/62606.

Council of Science Editors:

Ingram R. Label-free bioanalytical methods for investigating bimolecular interactions: A review. [Masters Thesis]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/62606


Georgia Tech

4. Kalelkar, Pranav Pratap. Synthesis of functional polylactides for biomedical and pharmaceutical applications.

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

 Polylactide (PL) is an aliphatic thermoplastic that has gained attention over the years as a result of it biocompatible and biodegradable behavior. These characteristics make… (more)

Subjects/Keywords: Polylactide; Poly(lactic acid); Functional copolylactides; Antimicrobial copolylactide

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APA (6th Edition):

Kalelkar, P. P. (2018). Synthesis of functional polylactides for biomedical and pharmaceutical applications. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/62609

Chicago Manual of Style (16th Edition):

Kalelkar, Pranav Pratap. “Synthesis of functional polylactides for biomedical and pharmaceutical applications.” 2018. Doctoral Dissertation, Georgia Tech. Accessed January 17, 2021. http://hdl.handle.net/1853/62609.

MLA Handbook (7th Edition):

Kalelkar, Pranav Pratap. “Synthesis of functional polylactides for biomedical and pharmaceutical applications.” 2018. Web. 17 Jan 2021.

Vancouver:

Kalelkar PP. Synthesis of functional polylactides for biomedical and pharmaceutical applications. [Internet] [Doctoral dissertation]. Georgia Tech; 2018. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1853/62609.

Council of Science Editors:

Kalelkar PP. Synthesis of functional polylactides for biomedical and pharmaceutical applications. [Doctoral Dissertation]. Georgia Tech; 2018. Available from: http://hdl.handle.net/1853/62609


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 17, 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. 17 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 17]. 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 17, 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. 17 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 17]. 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. Beveridge, Jennifer Marie. Click chemistry applications for surfaces.

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

 Copper(I) catalyzed azide alkyne cycloaddition (CuAAC) is a powerful tool that allows for diverse functionalization from azide and alkyne precursors. This research probed the kinetics… (more)

Subjects/Keywords: Click chemistry; Flexible PVC; SU-8 azidation; Vesicle reactivity

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APA (6th Edition):

Beveridge, J. M. (2018). Click chemistry applications for surfaces. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/62216

Chicago Manual of Style (16th Edition):

Beveridge, Jennifer Marie. “Click chemistry applications for surfaces.” 2018. Doctoral Dissertation, Georgia Tech. Accessed January 17, 2021. http://hdl.handle.net/1853/62216.

MLA Handbook (7th Edition):

Beveridge, Jennifer Marie. “Click chemistry applications for surfaces.” 2018. Web. 17 Jan 2021.

Vancouver:

Beveridge JM. Click chemistry applications for surfaces. [Internet] [Doctoral dissertation]. Georgia Tech; 2018. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1853/62216.

Council of Science Editors:

Beveridge JM. Click chemistry applications for surfaces. [Doctoral Dissertation]. Georgia Tech; 2018. Available from: http://hdl.handle.net/1853/62216


Georgia Tech

8. Gryder, Berkley Eric. New insights into targeting the androgen receptor for cancer therapy: from selective delivery of gold nanoparticles and histone deacetylase inhibitors, to potent antagonists and inverse agonists.

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

 Cancer is the second leading cause of death in the United States (more than half a million people each year), and even with billions of… (more)

Subjects/Keywords: Gold nanoparticle (AuNP); Epigenetics; Anticancer; Small molecules; Histone deacetylase inhibitors (HDACi); Androgen receptor (AR); Prostate cancer

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APA (6th Edition):

Gryder, B. E. (2013). New insights into targeting the androgen receptor for cancer therapy: from selective delivery of gold nanoparticles and histone deacetylase inhibitors, to potent antagonists and inverse agonists. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/52926

Chicago Manual of Style (16th Edition):

Gryder, Berkley Eric. “New insights into targeting the androgen receptor for cancer therapy: from selective delivery of gold nanoparticles and histone deacetylase inhibitors, to potent antagonists and inverse agonists.” 2013. Doctoral Dissertation, Georgia Tech. Accessed January 17, 2021. http://hdl.handle.net/1853/52926.

MLA Handbook (7th Edition):

Gryder, Berkley Eric. “New insights into targeting the androgen receptor for cancer therapy: from selective delivery of gold nanoparticles and histone deacetylase inhibitors, to potent antagonists and inverse agonists.” 2013. Web. 17 Jan 2021.

Vancouver:

Gryder BE. New insights into targeting the androgen receptor for cancer therapy: from selective delivery of gold nanoparticles and histone deacetylase inhibitors, to potent antagonists and inverse agonists. [Internet] [Doctoral dissertation]. Georgia Tech; 2013. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1853/52926.

Council of Science Editors:

Gryder BE. New insights into targeting the androgen receptor for cancer therapy: from selective delivery of gold nanoparticles and histone deacetylase inhibitors, to potent antagonists and inverse agonists. [Doctoral Dissertation]. Georgia Tech; 2013. Available from: http://hdl.handle.net/1853/52926


Georgia Tech

9. Sodji, Quaovi Hemeka. Improving histone deacetylase inhibition therapy through isoform selectivity and targeted delivery.

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

 Histone deacetylase (HDAC) inhibition has recently emerged as a novel therapy for cancer treatment. However, currently approved histone deacetylase inhibitors (HDACi) are pan-inhibitors thus inhibiting… (more)

Subjects/Keywords: Histone deacetylase (HDAC); HDAC inhibitors; Isoform selectivity; Targeted delivery

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APA (6th Edition):

Sodji, Q. H. (2014). Improving histone deacetylase inhibition therapy through isoform selectivity and targeted delivery. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53445

Chicago Manual of Style (16th Edition):

Sodji, Quaovi Hemeka. “Improving histone deacetylase inhibition therapy through isoform selectivity and targeted delivery.” 2014. Doctoral Dissertation, Georgia Tech. Accessed January 17, 2021. http://hdl.handle.net/1853/53445.

MLA Handbook (7th Edition):

Sodji, Quaovi Hemeka. “Improving histone deacetylase inhibition therapy through isoform selectivity and targeted delivery.” 2014. Web. 17 Jan 2021.

Vancouver:

Sodji QH. Improving histone deacetylase inhibition therapy through isoform selectivity and targeted delivery. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1853/53445.

Council of Science Editors:

Sodji QH. Improving histone deacetylase inhibition therapy through isoform selectivity and targeted delivery. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/53445


Georgia Tech

10. Pan, Chenyi. Role of histone H1 in neural differentiation of embryonic stem cells.

Degree: PhD, Biology, 2015, Georgia Tech

 Linker histone H1 is a key structural protein facilitating the formation of higher order chromatin structures and regulates specific gene expression. In mammals, there exist… (more)

Subjects/Keywords: Histone h1; Embryonic stem cells; Neural differentiation; Oct4; Mutation; Follicular lymphoma

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APA (6th Edition):

Pan, C. (2015). Role of histone H1 in neural differentiation of embryonic stem cells. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58557

Chicago Manual of Style (16th Edition):

Pan, Chenyi. “Role of histone H1 in neural differentiation of embryonic stem cells.” 2015. Doctoral Dissertation, Georgia Tech. Accessed January 17, 2021. http://hdl.handle.net/1853/58557.

MLA Handbook (7th Edition):

Pan, Chenyi. “Role of histone H1 in neural differentiation of embryonic stem cells.” 2015. Web. 17 Jan 2021.

Vancouver:

Pan C. Role of histone H1 in neural differentiation of embryonic stem cells. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1853/58557.

Council of Science Editors:

Pan C. Role of histone H1 in neural differentiation of embryonic stem cells. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/58557


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 17, 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. 17 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 17]. 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


Georgia Tech

12. Raji, Idris. Novel approaches towards the discovery of tumor-selective histone deacetylase inhibitors.

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

 Developing safer and/ or more effective chemotherapeutics has been a long-standing challenge in the drug discovery field. To address these shortcomings, the designed-multiple ligand (DML)… (more)

Subjects/Keywords: Histone deacetylase; HDACi; Cyclooxygenase; Macrolide; Clarithromycin; Melanoma; Designed-multiple ligand; Lung cancer; Prostate cancer; Liposome; PGE2; NF-kB; Celecoxib; Indomethacin; Benzamides; Androgen receptor

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APA (6th Edition):

Raji, I. (2016). Novel approaches towards the discovery of tumor-selective histone deacetylase inhibitors. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/59152

Chicago Manual of Style (16th Edition):

Raji, Idris. “Novel approaches towards the discovery of tumor-selective histone deacetylase inhibitors.” 2016. Doctoral Dissertation, Georgia Tech. Accessed January 17, 2021. http://hdl.handle.net/1853/59152.

MLA Handbook (7th Edition):

Raji, Idris. “Novel approaches towards the discovery of tumor-selective histone deacetylase inhibitors.” 2016. Web. 17 Jan 2021.

Vancouver:

Raji I. Novel approaches towards the discovery of tumor-selective histone deacetylase inhibitors. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1853/59152.

Council of Science Editors:

Raji I. Novel approaches towards the discovery of tumor-selective histone deacetylase inhibitors. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/59152


Georgia Tech

13. Williams, Corey Wayne. Novel (homo-)Nazarov approaches to complex polycycles and application to bioactive targets.

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

 Complex carbocycles and heterocycles make up a large majority of natural product scaffolds and active pharmaceutical ingredient cores. As a result of this, developing methods… (more)

Subjects/Keywords: Cyclopropane; Homo-Nazarov; Nazarov; Synthetic methodology; Natural product synthesis; Ring-opening; Ring-closing; Cyclohexanone; Friedel-Crafts; Antimalarial; Anticancer; Propolisbenzofuran; Catalysis; Chemodivergence

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APA (6th Edition):

Williams, C. W. (2018). Novel (homo-)Nazarov approaches to complex polycycles and application to bioactive targets. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60299

Chicago Manual of Style (16th Edition):

Williams, Corey Wayne. “Novel (homo-)Nazarov approaches to complex polycycles and application to bioactive targets.” 2018. Doctoral Dissertation, Georgia Tech. Accessed January 17, 2021. http://hdl.handle.net/1853/60299.

MLA Handbook (7th Edition):

Williams, Corey Wayne. “Novel (homo-)Nazarov approaches to complex polycycles and application to bioactive targets.” 2018. Web. 17 Jan 2021.

Vancouver:

Williams CW. Novel (homo-)Nazarov approaches to complex polycycles and application to bioactive targets. [Internet] [Doctoral dissertation]. Georgia Tech; 2018. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1853/60299.

Council of Science Editors:

Williams CW. Novel (homo-)Nazarov approaches to complex polycycles and application to bioactive targets. [Doctoral Dissertation]. Georgia Tech; 2018. Available from: http://hdl.handle.net/1853/60299


Georgia Tech

14. Poulin, Remington X. Waves of communication: Metabolomics describe the nature and role of waterborne cues in the marine environment.

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

 Waterborne cues are important tools for signaling in the marine environment. Despite decades of dedicated research, we know little about the chemical nature of these… (more)

Subjects/Keywords: Chemical ecology; Waterborne cues; Metabolomics

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APA (6th Edition):

Poulin, R. X. (2017). Waves of communication: Metabolomics describe the nature and role of waterborne cues in the marine environment. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60712

Chicago Manual of Style (16th Edition):

Poulin, Remington X. “Waves of communication: Metabolomics describe the nature and role of waterborne cues in the marine environment.” 2017. Doctoral Dissertation, Georgia Tech. Accessed January 17, 2021. http://hdl.handle.net/1853/60712.

MLA Handbook (7th Edition):

Poulin, Remington X. “Waves of communication: Metabolomics describe the nature and role of waterborne cues in the marine environment.” 2017. Web. 17 Jan 2021.

Vancouver:

Poulin RX. Waves of communication: Metabolomics describe the nature and role of waterborne cues in the marine environment. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1853/60712.

Council of Science Editors:

Poulin RX. Waves of communication: Metabolomics describe the nature and role of waterborne cues in the marine environment. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/60712

15. Watson, Ryan A. Identification of redox-linked structural changes in ribonucleotide reductase (RNR) by way of reaction-induced FTIR spectroscopy.

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

 Ribonucleotide reductase (RNR) catalyzes the production of deoxyribonucleotides in all cells. In E. coli class Ia RNR, a transient 2β2 complex forms when a ribonucleotide… (more)

Subjects/Keywords: Ribonucleotide reductase; FTIR spectroscopy; Tyrosyl radical

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APA (6th Edition):

Watson, R. A. (2018). Identification of redox-linked structural changes in ribonucleotide reductase (RNR) by way of reaction-induced FTIR spectroscopy. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/61665

Chicago Manual of Style (16th Edition):

Watson, Ryan A. “Identification of redox-linked structural changes in ribonucleotide reductase (RNR) by way of reaction-induced FTIR spectroscopy.” 2018. Doctoral Dissertation, Georgia Tech. Accessed January 17, 2021. http://hdl.handle.net/1853/61665.

MLA Handbook (7th Edition):

Watson, Ryan A. “Identification of redox-linked structural changes in ribonucleotide reductase (RNR) by way of reaction-induced FTIR spectroscopy.” 2018. Web. 17 Jan 2021.

Vancouver:

Watson RA. Identification of redox-linked structural changes in ribonucleotide reductase (RNR) by way of reaction-induced FTIR spectroscopy. [Internet] [Doctoral dissertation]. Georgia Tech; 2018. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1853/61665.

Council of Science Editors:

Watson RA. Identification of redox-linked structural changes in ribonucleotide reductase (RNR) by way of reaction-induced FTIR spectroscopy. [Doctoral Dissertation]. Georgia Tech; 2018. Available from: http://hdl.handle.net/1853/61665


Georgia Tech

16. 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 17, 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. 17 Jan 2021.

Vancouver:

Donegan RK. Structural and biophysical characterization of the myocilin olfactomedin domain. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2021 Jan 17]. 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

17. Sun, Qining. Effect of lignin content and structural change during treatment on poplar for biofuel and biomaterial production.

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

 Understanding the lignin effect and related structural parameters relevant to the recalcitrance of the plant cell wall and the individual and cooperative effects on enzymatic… (more)

Subjects/Keywords: Lignin; Poplar; Cellulose ultrastructure; Dilute acid pretreatment; Carbon fiber precursor; Biofuel; Biomaterial.

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APA (6th Edition):

Sun, Q. (2015). Effect of lignin content and structural change during treatment on poplar for biofuel and biomaterial production. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54885

Chicago Manual of Style (16th Edition):

Sun, Qining. “Effect of lignin content and structural change during treatment on poplar for biofuel and biomaterial production.” 2015. Doctoral Dissertation, Georgia Tech. Accessed January 17, 2021. http://hdl.handle.net/1853/54885.

MLA Handbook (7th Edition):

Sun, Qining. “Effect of lignin content and structural change during treatment on poplar for biofuel and biomaterial production.” 2015. Web. 17 Jan 2021.

Vancouver:

Sun Q. Effect of lignin content and structural change during treatment on poplar for biofuel and biomaterial production. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1853/54885.

Council of Science Editors:

Sun Q. Effect of lignin content and structural change during treatment on poplar for biofuel and biomaterial production. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/54885


Georgia Tech

18. Aponte-Guzman, Joel. Ring-opening benzannulations of cyclopropenes, alkylidene cyclopropanes, and 2,3-dihydrofuran acetals: A complementary approach to benzo-fused (hetero)aromatics.

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

 Over the past decades, functional group manipulation of aromatic precursors has been a common strategy to access new aromatic compounds. However, these classical methods, such… (more)

Subjects/Keywords: Cyclopropenes; Alkylidene cyclopropanes; 2,3-dihydrofuran; Benzo-fused aromatics; Benzannulation; Ring-opening; Formal-homo-Nazarov cyclization; Heteroaromatics

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APA (6th Edition):

Aponte-Guzman, J. (2016). Ring-opening benzannulations of cyclopropenes, alkylidene cyclopropanes, and 2,3-dihydrofuran acetals: A complementary approach to benzo-fused (hetero)aromatics. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54953

Chicago Manual of Style (16th Edition):

Aponte-Guzman, Joel. “Ring-opening benzannulations of cyclopropenes, alkylidene cyclopropanes, and 2,3-dihydrofuran acetals: A complementary approach to benzo-fused (hetero)aromatics.” 2016. Doctoral Dissertation, Georgia Tech. Accessed January 17, 2021. http://hdl.handle.net/1853/54953.

MLA Handbook (7th Edition):

Aponte-Guzman, Joel. “Ring-opening benzannulations of cyclopropenes, alkylidene cyclopropanes, and 2,3-dihydrofuran acetals: A complementary approach to benzo-fused (hetero)aromatics.” 2016. Web. 17 Jan 2021.

Vancouver:

Aponte-Guzman J. Ring-opening benzannulations of cyclopropenes, alkylidene cyclopropanes, and 2,3-dihydrofuran acetals: A complementary approach to benzo-fused (hetero)aromatics. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1853/54953.

Council of Science Editors:

Aponte-Guzman J. Ring-opening benzannulations of cyclopropenes, alkylidene cyclopropanes, and 2,3-dihydrofuran acetals: A complementary approach to benzo-fused (hetero)aromatics. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/54953


Georgia Tech

19. 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 17, 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. 17 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 17]. 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

20. Shenje, Raynold. Strained carbocycles as gateways to polycyclic molecular scaffolds and natural products targets.

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

 Cyclopropanes and cyclobutanes, when activated with donor and acceptor groups, provide facile access to a plethora of interesting chemical scaffolds. Importantly, D-A cyclopropanes and cyclobutanes… (more)

Subjects/Keywords: Ring-opening; Strained carbocyles; Lewis acid catalysis; Natural products scaffolds

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APA (6th Edition):

Shenje, R. (2016). Strained carbocycles as gateways to polycyclic molecular scaffolds and natural products targets. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/55673

Chicago Manual of Style (16th Edition):

Shenje, Raynold. “Strained carbocycles as gateways to polycyclic molecular scaffolds and natural products targets.” 2016. Doctoral Dissertation, Georgia Tech. Accessed January 17, 2021. http://hdl.handle.net/1853/55673.

MLA Handbook (7th Edition):

Shenje, Raynold. “Strained carbocycles as gateways to polycyclic molecular scaffolds and natural products targets.” 2016. Web. 17 Jan 2021.

Vancouver:

Shenje R. Strained carbocycles as gateways to polycyclic molecular scaffolds and natural products targets. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1853/55673.

Council of Science Editors:

Shenje R. Strained carbocycles as gateways to polycyclic molecular scaffolds and natural products targets. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/55673


Georgia Tech

21. Fathi, Shaghayegh. Targeted delivery of histone deacetylase inhibitors for use in cancer therapy.

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

 Cancer is one of the leading causes of death around the world, with lung, breast and prostate cancer being the most common cancers. Most of… (more)

Subjects/Keywords: Cancer; Histone deacetylase; Histone deacetylase inhibitors; Targeted delivery; Azithromycin; Tamoxifen; SAHA; Pyrimethamine; Liposome

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APA (6th Edition):

Fathi, S. (2016). Targeted delivery of histone deacetylase inhibitors for use in cancer therapy. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/61091

Chicago Manual of Style (16th Edition):

Fathi, Shaghayegh. “Targeted delivery of histone deacetylase inhibitors for use in cancer therapy.” 2016. Doctoral Dissertation, Georgia Tech. Accessed January 17, 2021. http://hdl.handle.net/1853/61091.

MLA Handbook (7th Edition):

Fathi, Shaghayegh. “Targeted delivery of histone deacetylase inhibitors for use in cancer therapy.” 2016. Web. 17 Jan 2021.

Vancouver:

Fathi S. Targeted delivery of histone deacetylase inhibitors for use in cancer therapy. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1853/61091.

Council of Science Editors:

Fathi S. Targeted delivery of histone deacetylase inhibitors for use in cancer therapy. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/61091


Georgia Tech

22. 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 17, 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. 17 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 17]. 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

23. 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 17, 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. 17 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 17]. 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

24. 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 17, 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. 17 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 17]. 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

25. Patil, Vishal. Design and synthesis of small molecule inhibitors of zinc metalloenzymes.

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

 Histone deacetylases (HDACs) are a class of enzymes that play a crucial role in DNA expression by removing an acetyl group from the ɛ-N-acetyl lysine… (more)

Subjects/Keywords: Bifunctional inhibitors; Isoform selectivity; Spliceosome assembly inhibitors; Leishmania; Malaria; Histone deacetylase inhibitors; Cancer chemotherapy; Zinc binding groups; Metalloenzymes; Enzymes; Metalloproteins

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APA (6th Edition):

Patil, V. (2011). Design and synthesis of small molecule inhibitors of zinc metalloenzymes. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/45859

Chicago Manual of Style (16th Edition):

Patil, Vishal. “Design and synthesis of small molecule inhibitors of zinc metalloenzymes.” 2011. Doctoral Dissertation, Georgia Tech. Accessed January 17, 2021. http://hdl.handle.net/1853/45859.

MLA Handbook (7th Edition):

Patil, Vishal. “Design and synthesis of small molecule inhibitors of zinc metalloenzymes.” 2011. Web. 17 Jan 2021.

Vancouver:

Patil V. Design and synthesis of small molecule inhibitors of zinc metalloenzymes. [Internet] [Doctoral dissertation]. Georgia Tech; 2011. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1853/45859.

Council of Science Editors:

Patil V. Design and synthesis of small molecule inhibitors of zinc metalloenzymes. [Doctoral Dissertation]. Georgia Tech; 2011. Available from: http://hdl.handle.net/1853/45859

26. 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 17, 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. 17 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 17]. 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

27. Johnson, Jennifer Leigh. The quest for a general co-crystallization strategy for macromolecules: lessons on the use of chaperones for membrane protein crystallization.

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

 Crystallization is often a major bottleneck to macromolecular structure determination. This is particularly true for membrane proteins, which have hydrophobic surfaces that cannot readily form… (more)

Subjects/Keywords: Fab fragment; Fabry disease; Crystallography; Membrane protein; Antibody fragment; Crystallization chaperone; Monomeric streptavidin; Signal peptide peptidase; Intimin; Alpha-galactosidase A; Pharmacological chaperone

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APA (6th Edition):

Johnson, J. L. (2015). The quest for a general co-crystallization strategy for macromolecules: lessons on the use of chaperones for membrane protein crystallization. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53886

Chicago Manual of Style (16th Edition):

Johnson, Jennifer Leigh. “The quest for a general co-crystallization strategy for macromolecules: lessons on the use of chaperones for membrane protein crystallization.” 2015. Doctoral Dissertation, Georgia Tech. Accessed January 17, 2021. http://hdl.handle.net/1853/53886.

MLA Handbook (7th Edition):

Johnson, Jennifer Leigh. “The quest for a general co-crystallization strategy for macromolecules: lessons on the use of chaperones for membrane protein crystallization.” 2015. Web. 17 Jan 2021.

Vancouver:

Johnson JL. The quest for a general co-crystallization strategy for macromolecules: lessons on the use of chaperones for membrane protein crystallization. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1853/53886.

Council of Science Editors:

Johnson JL. The quest for a general co-crystallization strategy for macromolecules: lessons on the use of chaperones for membrane protein crystallization. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/53886

28. Chen, Po Chih. Design and synthesis of small molecules and nanoparticle conjugates for cell type-selective delivery.

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

 Histone deacetylase (HDAC) inhibition is an emerging novel therapeutic strategy in cancer therapy. HDAC inhibitors (HDACi) have shown ability to block angiogenesis and cell cycling,… (more)

Subjects/Keywords: Histone deacetylase; Gold nanoparticles; Penicillin; Click chemistry; Diazo-transfer reaction; Nonpeptide macrolide; Bioconjugates; Molecules; Nanostructures; Bioavailability; Drug delivery systems

…to my success as a chemist at Georgia Tech. I would also like to thank JP, Katy, and Lisa… …all of their help and friendship in my early years at Georgia Tech. Because of everyone… 

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APA (6th Edition):

Chen, P. C. (2009). Design and synthesis of small molecules and nanoparticle conjugates for cell type-selective delivery. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/28111

Chicago Manual of Style (16th Edition):

Chen, Po Chih. “Design and synthesis of small molecules and nanoparticle conjugates for cell type-selective delivery.” 2009. Doctoral Dissertation, Georgia Tech. Accessed January 17, 2021. http://hdl.handle.net/1853/28111.

MLA Handbook (7th Edition):

Chen, Po Chih. “Design and synthesis of small molecules and nanoparticle conjugates for cell type-selective delivery.” 2009. Web. 17 Jan 2021.

Vancouver:

Chen PC. Design and synthesis of small molecules and nanoparticle conjugates for cell type-selective delivery. [Internet] [Doctoral dissertation]. Georgia Tech; 2009. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1853/28111.

Council of Science Editors:

Chen PC. Design and synthesis of small molecules and nanoparticle conjugates for cell type-selective delivery. [Doctoral Dissertation]. Georgia Tech; 2009. Available from: http://hdl.handle.net/1853/28111

29. 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 17, 2021. http://hdl.handle.net/1853/29739.

MLA Handbook (7th Edition):

Persil Cetinkol, Ozgul. “Small molecule recognition of homopurine nucleic acid structures.” 2008. Web. 17 Jan 2021.

Vancouver:

Persil Cetinkol O. Small molecule recognition of homopurine nucleic acid structures. [Internet] [Doctoral dissertation]. Georgia Tech; 2008. [cited 2021 Jan 17]. 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

30. Patil, Dadasaheb V. Intramolecular cyclization strategies for synthesizing medium-ring polycycles and the total synthesis of natural products.

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

 Carbo- and heterocyclic compounds are of great interest to chemists. Intramolecular cyclization strategies of donor-acceptor (D-A) cyclopropanes and alkylidene malonate monoamides have excellent potential for… (more)

Subjects/Keywords: Donor-acceptor cyclopropanes; Indium catalysis; Formal homo-Nazarov reaction; Friedel-Crafts reaction; Intramolecular cyclizations; Tandem reactions; Alkylidene malonate monoamides; Heterocyclic compounds; Polycyclic compounds

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APA (6th Edition):

Patil, D. V. (2012). Intramolecular cyclization strategies for synthesizing medium-ring polycycles and the total synthesis of natural products. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/50118

Chicago Manual of Style (16th Edition):

Patil, Dadasaheb V. “Intramolecular cyclization strategies for synthesizing medium-ring polycycles and the total synthesis of natural products.” 2012. Doctoral Dissertation, Georgia Tech. Accessed January 17, 2021. http://hdl.handle.net/1853/50118.

MLA Handbook (7th Edition):

Patil, Dadasaheb V. “Intramolecular cyclization strategies for synthesizing medium-ring polycycles and the total synthesis of natural products.” 2012. Web. 17 Jan 2021.

Vancouver:

Patil DV. Intramolecular cyclization strategies for synthesizing medium-ring polycycles and the total synthesis of natural products. [Internet] [Doctoral dissertation]. Georgia Tech; 2012. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1853/50118.

Council of Science Editors:

Patil DV. Intramolecular cyclization strategies for synthesizing medium-ring polycycles and the total synthesis of natural products. [Doctoral Dissertation]. Georgia Tech; 2012. Available from: http://hdl.handle.net/1853/50118

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