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You searched for +publisher:"Georgia State University" +contributor:("Dr. Giovanni Gadda"). Showing records 1 – 17 of 17 total matches.

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Georgia State University

1. Yuan, Hongling. Mechanistic Studies of Two Selected Flavin-Dependent Enzymes: Choline Oxidase and D-Arginine Dehydrogenase.

Degree: PhD, Chemistry, 2011, Georgia State University

  Choline oxidase catalyzes the flavin-dependent, two-step oxidation of choline to glycine betaine via the formation of an aldehyde intermediate. The oxidation of choline includes… (more)

Subjects/Keywords: Choline oxidase; Hydroxyl group; C4a-cysteinyl adduct; D-arginine dehydrogenase; Conformational change; Hydride transfer; Chemistry

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APA (6th Edition):

Yuan, H. (2011). Mechanistic Studies of Two Selected Flavin-Dependent Enzymes: Choline Oxidase and D-Arginine Dehydrogenase. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_diss/56

Chicago Manual of Style (16th Edition):

Yuan, Hongling. “Mechanistic Studies of Two Selected Flavin-Dependent Enzymes: Choline Oxidase and D-Arginine Dehydrogenase.” 2011. Doctoral Dissertation, Georgia State University. Accessed June 19, 2019. https://scholarworks.gsu.edu/chemistry_diss/56.

MLA Handbook (7th Edition):

Yuan, Hongling. “Mechanistic Studies of Two Selected Flavin-Dependent Enzymes: Choline Oxidase and D-Arginine Dehydrogenase.” 2011. Web. 19 Jun 2019.

Vancouver:

Yuan H. Mechanistic Studies of Two Selected Flavin-Dependent Enzymes: Choline Oxidase and D-Arginine Dehydrogenase. [Internet] [Doctoral dissertation]. Georgia State University; 2011. [cited 2019 Jun 19]. Available from: https://scholarworks.gsu.edu/chemistry_diss/56.

Council of Science Editors:

Yuan H. Mechanistic Studies of Two Selected Flavin-Dependent Enzymes: Choline Oxidase and D-Arginine Dehydrogenase. [Doctoral Dissertation]. Georgia State University; 2011. Available from: https://scholarworks.gsu.edu/chemistry_diss/56


Georgia State University

2. Gannavaram, Swathi. Mechanistic Enzymology of Flavin-dependent Catalysis in Bacterial D-Arginine Dehydrogenase and Choline Oxidase.

Degree: PhD, Chemistry, 2014, Georgia State University

  D-Arginine dehydrogenase (DADH) catalyzes the oxidation of D-arginine to imino arginine using FAD as the cofactor. The enzyme is part of a recently discovered… (more)

Subjects/Keywords: D-Arginine dehydrogenase; Choline oxidase; FAD; Reductive half-reaction; Hydride transfer; Oxidative half-reaction; Molecular O2

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APA (6th Edition):

Gannavaram, S. (2014). Mechanistic Enzymology of Flavin-dependent Catalysis in Bacterial D-Arginine Dehydrogenase and Choline Oxidase. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_diss/93

Chicago Manual of Style (16th Edition):

Gannavaram, Swathi. “Mechanistic Enzymology of Flavin-dependent Catalysis in Bacterial D-Arginine Dehydrogenase and Choline Oxidase.” 2014. Doctoral Dissertation, Georgia State University. Accessed June 19, 2019. https://scholarworks.gsu.edu/chemistry_diss/93.

MLA Handbook (7th Edition):

Gannavaram, Swathi. “Mechanistic Enzymology of Flavin-dependent Catalysis in Bacterial D-Arginine Dehydrogenase and Choline Oxidase.” 2014. Web. 19 Jun 2019.

Vancouver:

Gannavaram S. Mechanistic Enzymology of Flavin-dependent Catalysis in Bacterial D-Arginine Dehydrogenase and Choline Oxidase. [Internet] [Doctoral dissertation]. Georgia State University; 2014. [cited 2019 Jun 19]. Available from: https://scholarworks.gsu.edu/chemistry_diss/93.

Council of Science Editors:

Gannavaram S. Mechanistic Enzymology of Flavin-dependent Catalysis in Bacterial D-Arginine Dehydrogenase and Choline Oxidase. [Doctoral Dissertation]. Georgia State University; 2014. Available from: https://scholarworks.gsu.edu/chemistry_diss/93

3. Uluisik, Rizvan C. Effects of Temperature on the Kinetic Isotope Effects for Proton and Hydride Transfers in the Active Site Variant of Choline Oxidase Ser101Ala.

Degree: MS, Chemistry, 2013, Georgia State University

  Choline oxidase catalyzes the oxidation of choline to glycine betaine. The reaction includes betaine aldehyde as an intermediate. FAD is reduced by the alcohol… (more)

Subjects/Keywords: Choline oxidase; Quantum tunneling; Proton transfer; Hydride transfer; Kinetic complexity

…in choline oxidase (unpublished data, Dr. Giovanni Gadda and Crystal Simitherman)… 

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APA (6th Edition):

Uluisik, R. C. (2013). Effects of Temperature on the Kinetic Isotope Effects for Proton and Hydride Transfers in the Active Site Variant of Choline Oxidase Ser101Ala. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_theses/56

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

Chicago Manual of Style (16th Edition):

Uluisik, Rizvan C. “Effects of Temperature on the Kinetic Isotope Effects for Proton and Hydride Transfers in the Active Site Variant of Choline Oxidase Ser101Ala.” 2013. Thesis, Georgia State University. Accessed June 19, 2019. https://scholarworks.gsu.edu/chemistry_theses/56.

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

MLA Handbook (7th Edition):

Uluisik, Rizvan C. “Effects of Temperature on the Kinetic Isotope Effects for Proton and Hydride Transfers in the Active Site Variant of Choline Oxidase Ser101Ala.” 2013. Web. 19 Jun 2019.

Vancouver:

Uluisik RC. Effects of Temperature on the Kinetic Isotope Effects for Proton and Hydride Transfers in the Active Site Variant of Choline Oxidase Ser101Ala. [Internet] [Thesis]. Georgia State University; 2013. [cited 2019 Jun 19]. Available from: https://scholarworks.gsu.edu/chemistry_theses/56.

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

Council of Science Editors:

Uluisik RC. Effects of Temperature on the Kinetic Isotope Effects for Proton and Hydride Transfers in the Active Site Variant of Choline Oxidase Ser101Ala. [Thesis]. Georgia State University; 2013. Available from: https://scholarworks.gsu.edu/chemistry_theses/56

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


Georgia State University

4. Flores, Elias. Cloning, Purification, and Biochemical Characterization of PA1225, a Novel FAD Containing NADPH:Quinone Reductase from Pseudomonas aeruginosa PAO1.

Degree: MS, Chemistry, 2017, Georgia State University

  The gene product of pa1225 found in the opportunistic bacterium Pseudomonas aeruginosa strain PAO1 is currently annotated as a putative NAD(P)H dehydrogenase. Prior investigation… (more)

Subjects/Keywords: PA1225; NADH; NADPH; Pseudomonas aeruginosa; reductive-half reaction; steady-state; quinone; LysR; detoxifying.

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APA (6th Edition):

Flores, E. (2017). Cloning, Purification, and Biochemical Characterization of PA1225, a Novel FAD Containing NADPH:Quinone Reductase from Pseudomonas aeruginosa PAO1. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_theses/112

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

Chicago Manual of Style (16th Edition):

Flores, Elias. “Cloning, Purification, and Biochemical Characterization of PA1225, a Novel FAD Containing NADPH:Quinone Reductase from Pseudomonas aeruginosa PAO1.” 2017. Thesis, Georgia State University. Accessed June 19, 2019. https://scholarworks.gsu.edu/chemistry_theses/112.

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

MLA Handbook (7th Edition):

Flores, Elias. “Cloning, Purification, and Biochemical Characterization of PA1225, a Novel FAD Containing NADPH:Quinone Reductase from Pseudomonas aeruginosa PAO1.” 2017. Web. 19 Jun 2019.

Vancouver:

Flores E. Cloning, Purification, and Biochemical Characterization of PA1225, a Novel FAD Containing NADPH:Quinone Reductase from Pseudomonas aeruginosa PAO1. [Internet] [Thesis]. Georgia State University; 2017. [cited 2019 Jun 19]. Available from: https://scholarworks.gsu.edu/chemistry_theses/112.

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

Council of Science Editors:

Flores E. Cloning, Purification, and Biochemical Characterization of PA1225, a Novel FAD Containing NADPH:Quinone Reductase from Pseudomonas aeruginosa PAO1. [Thesis]. Georgia State University; 2017. Available from: https://scholarworks.gsu.edu/chemistry_theses/112

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


Georgia State University

5. Smitherman, Crystal L. Biochemical and Mechanistic Studies of Nitronate Monooxygenase and Roles of Histidine Residues in Select Flavoprotein Oxidases.

Degree: PhD, Chemistry, 2015, Georgia State University

  Nitronate monooxygenase (NMO) catalyzes the flavin-dependent oxidation of propionate 3-nitronate (P3N) via the formation of an anionic flavosemiquinone. The oxidation of substrate includes the… (more)

Subjects/Keywords: Nitronate monooxygenase; choline oxidase; fluorescence spectroscopy; propionate 3-nitronate; electron transfer circular dichroism

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APA (6th Edition):

Smitherman, C. L. (2015). Biochemical and Mechanistic Studies of Nitronate Monooxygenase and Roles of Histidine Residues in Select Flavoprotein Oxidases. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_diss/112

Chicago Manual of Style (16th Edition):

Smitherman, Crystal L. “Biochemical and Mechanistic Studies of Nitronate Monooxygenase and Roles of Histidine Residues in Select Flavoprotein Oxidases.” 2015. Doctoral Dissertation, Georgia State University. Accessed June 19, 2019. https://scholarworks.gsu.edu/chemistry_diss/112.

MLA Handbook (7th Edition):

Smitherman, Crystal L. “Biochemical and Mechanistic Studies of Nitronate Monooxygenase and Roles of Histidine Residues in Select Flavoprotein Oxidases.” 2015. Web. 19 Jun 2019.

Vancouver:

Smitherman CL. Biochemical and Mechanistic Studies of Nitronate Monooxygenase and Roles of Histidine Residues in Select Flavoprotein Oxidases. [Internet] [Doctoral dissertation]. Georgia State University; 2015. [cited 2019 Jun 19]. Available from: https://scholarworks.gsu.edu/chemistry_diss/112.

Council of Science Editors:

Smitherman CL. Biochemical and Mechanistic Studies of Nitronate Monooxygenase and Roles of Histidine Residues in Select Flavoprotein Oxidases. [Doctoral Dissertation]. Georgia State University; 2015. Available from: https://scholarworks.gsu.edu/chemistry_diss/112


Georgia State University

6. Delgado, Malcom Arturo. Biochemical Study of Engineered Fluorescent Proteins as Calcium Sensors and the Effect of Calcium and PH in Cell Reproduction and Protein Expression.

Degree: MS, Chemistry, 2009, Georgia State University

 Calcium plays important roles in both eukaryotic and prokaryotic cells. Its actions help to stabilize cell synthesis, growth and development. In this thesis, studies have… (more)

Subjects/Keywords: Calcium; Protein mCherry; Green Fluorescent Protein (GFP); E. coli. X-ray crystallography; Protein expression; Fluorescent proteins; BL21(DE3).

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APA (6th Edition):

Delgado, M. A. (2009). Biochemical Study of Engineered Fluorescent Proteins as Calcium Sensors and the Effect of Calcium and PH in Cell Reproduction and Protein Expression. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_theses/23

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

Chicago Manual of Style (16th Edition):

Delgado, Malcom Arturo. “Biochemical Study of Engineered Fluorescent Proteins as Calcium Sensors and the Effect of Calcium and PH in Cell Reproduction and Protein Expression.” 2009. Thesis, Georgia State University. Accessed June 19, 2019. https://scholarworks.gsu.edu/chemistry_theses/23.

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

MLA Handbook (7th Edition):

Delgado, Malcom Arturo. “Biochemical Study of Engineered Fluorescent Proteins as Calcium Sensors and the Effect of Calcium and PH in Cell Reproduction and Protein Expression.” 2009. Web. 19 Jun 2019.

Vancouver:

Delgado MA. Biochemical Study of Engineered Fluorescent Proteins as Calcium Sensors and the Effect of Calcium and PH in Cell Reproduction and Protein Expression. [Internet] [Thesis]. Georgia State University; 2009. [cited 2019 Jun 19]. Available from: https://scholarworks.gsu.edu/chemistry_theses/23.

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

Council of Science Editors:

Delgado MA. Biochemical Study of Engineered Fluorescent Proteins as Calcium Sensors and the Effect of Calcium and PH in Cell Reproduction and Protein Expression. [Thesis]. Georgia State University; 2009. Available from: https://scholarworks.gsu.edu/chemistry_theses/23

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


Georgia State University

7. Elangwe, Emilia N. Site Directed Mutagenesis, Expression and Enzymatic Studies of the 60 kDa Human HIV-TAT 1 Interactive Protein, TIP60.

Degree: MS, Chemistry, 2009, Georgia State University

 Tip60 is a 60 kDa nuclear protein which exists in three isoforms, belongs to the MYST/HAT family of proteins and was discovered after its interaction… (more)

Subjects/Keywords: Tip60; Site-directed mutagenesis; HATs; His-tagged Protein Expression; HAT assay; Post-translational modification; Tip60 catalysis; Chromatin modification; Histones; Chromatin; MYST family HATs; Histone acetylation and HAT inhibitors

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APA (6th Edition):

Elangwe, E. N. (2009). Site Directed Mutagenesis, Expression and Enzymatic Studies of the 60 kDa Human HIV-TAT 1 Interactive Protein, TIP60. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_theses/21

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

Chicago Manual of Style (16th Edition):

Elangwe, Emilia N. “Site Directed Mutagenesis, Expression and Enzymatic Studies of the 60 kDa Human HIV-TAT 1 Interactive Protein, TIP60.” 2009. Thesis, Georgia State University. Accessed June 19, 2019. https://scholarworks.gsu.edu/chemistry_theses/21.

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

MLA Handbook (7th Edition):

Elangwe, Emilia N. “Site Directed Mutagenesis, Expression and Enzymatic Studies of the 60 kDa Human HIV-TAT 1 Interactive Protein, TIP60.” 2009. Web. 19 Jun 2019.

Vancouver:

Elangwe EN. Site Directed Mutagenesis, Expression and Enzymatic Studies of the 60 kDa Human HIV-TAT 1 Interactive Protein, TIP60. [Internet] [Thesis]. Georgia State University; 2009. [cited 2019 Jun 19]. Available from: https://scholarworks.gsu.edu/chemistry_theses/21.

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

Council of Science Editors:

Elangwe EN. Site Directed Mutagenesis, Expression and Enzymatic Studies of the 60 kDa Human HIV-TAT 1 Interactive Protein, TIP60. [Thesis]. Georgia State University; 2009. Available from: https://scholarworks.gsu.edu/chemistry_theses/21

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


Georgia State University

8. Rungsrisuriyachai, Kunchala. On the Catalytic Roles of HIS351, ASN510, and HIS466 in Choline Oxidase and the Kinetic Mechanism of Pyranose 2-Oxidase.

Degree: PhD, Chemistry, 2010, Georgia State University

 Choline oxidase (E.C. 1.1.3.17) from Arthrobacter globiformis catalyzes the four-electron oxidation of choline to glycine betaine (N,N,N-trimethylglycine) via two sequential, FAD-dependent reactions in which betaine… (more)

Subjects/Keywords: flavin; Oxidase; kinetic isotope effects; steady-state kinetic mechanism; enzyme; mechanism; kinetic; Chemistry

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APA (6th Edition):

Rungsrisuriyachai, K. (2010). On the Catalytic Roles of HIS351, ASN510, and HIS466 in Choline Oxidase and the Kinetic Mechanism of Pyranose 2-Oxidase. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_diss/36

Chicago Manual of Style (16th Edition):

Rungsrisuriyachai, Kunchala. “On the Catalytic Roles of HIS351, ASN510, and HIS466 in Choline Oxidase and the Kinetic Mechanism of Pyranose 2-Oxidase.” 2010. Doctoral Dissertation, Georgia State University. Accessed June 19, 2019. https://scholarworks.gsu.edu/chemistry_diss/36.

MLA Handbook (7th Edition):

Rungsrisuriyachai, Kunchala. “On the Catalytic Roles of HIS351, ASN510, and HIS466 in Choline Oxidase and the Kinetic Mechanism of Pyranose 2-Oxidase.” 2010. Web. 19 Jun 2019.

Vancouver:

Rungsrisuriyachai K. On the Catalytic Roles of HIS351, ASN510, and HIS466 in Choline Oxidase and the Kinetic Mechanism of Pyranose 2-Oxidase. [Internet] [Doctoral dissertation]. Georgia State University; 2010. [cited 2019 Jun 19]. Available from: https://scholarworks.gsu.edu/chemistry_diss/36.

Council of Science Editors:

Rungsrisuriyachai K. On the Catalytic Roles of HIS351, ASN510, and HIS466 in Choline Oxidase and the Kinetic Mechanism of Pyranose 2-Oxidase. [Doctoral Dissertation]. Georgia State University; 2010. Available from: https://scholarworks.gsu.edu/chemistry_diss/36


Georgia State University

9. Caton-Williams, Julianne Marie. Synthesis and Enzymatic Studies of Selenium Derivatized Nucleosides, Nucleotides and Nucleic Acids.

Degree: PhD, Chemistry, 2009, Georgia State University

 Nucleoside 5-triphosphates are the building blocks to synthesis of nucleic acids. Nucleic acids (RNA and DNA) participate in many important biological functions in living systems,… (more)

Subjects/Keywords: Colored 4-selenothymidine; Plasmid; Klenow polymerase; Bathrochromic shift; Deoxynucleoside 5½-(½-P-seleno)triphosphates; Stability; Nucleic acids; Nucleoside 5½-triphosphates; Selenium-derivatized DNA; DNA flexibility; Duplex recognition; Chemistry

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APA (6th Edition):

Caton-Williams, J. M. (2009). Synthesis and Enzymatic Studies of Selenium Derivatized Nucleosides, Nucleotides and Nucleic Acids. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_diss/42

Chicago Manual of Style (16th Edition):

Caton-Williams, Julianne Marie. “Synthesis and Enzymatic Studies of Selenium Derivatized Nucleosides, Nucleotides and Nucleic Acids.” 2009. Doctoral Dissertation, Georgia State University. Accessed June 19, 2019. https://scholarworks.gsu.edu/chemistry_diss/42.

MLA Handbook (7th Edition):

Caton-Williams, Julianne Marie. “Synthesis and Enzymatic Studies of Selenium Derivatized Nucleosides, Nucleotides and Nucleic Acids.” 2009. Web. 19 Jun 2019.

Vancouver:

Caton-Williams JM. Synthesis and Enzymatic Studies of Selenium Derivatized Nucleosides, Nucleotides and Nucleic Acids. [Internet] [Doctoral dissertation]. Georgia State University; 2009. [cited 2019 Jun 19]. Available from: https://scholarworks.gsu.edu/chemistry_diss/42.

Council of Science Editors:

Caton-Williams JM. Synthesis and Enzymatic Studies of Selenium Derivatized Nucleosides, Nucleotides and Nucleic Acids. [Doctoral Dissertation]. Georgia State University; 2009. Available from: https://scholarworks.gsu.edu/chemistry_diss/42


Georgia State University

10. White, Natalie. Optimization of Expression and Purification Methods for the Study of Protein-Based Magnetic Resonance Imaging Contrast Agents.

Degree: MS, Chemistry, 2011, Georgia State University

  Magnetic Resonance Imaging instruments rely on a contrast agent to provide high-resolution images of tissues in vivo. However, current clinical contrast agents are hindered… (more)

Subjects/Keywords: Magnetic Resonance Imaging; Contrast agents; Relaxivity; Gadolinium; GST; Refolding method.

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APA (6th Edition):

White, N. (2011). Optimization of Expression and Purification Methods for the Study of Protein-Based Magnetic Resonance Imaging Contrast Agents. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_theses/42

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

Chicago Manual of Style (16th Edition):

White, Natalie. “Optimization of Expression and Purification Methods for the Study of Protein-Based Magnetic Resonance Imaging Contrast Agents.” 2011. Thesis, Georgia State University. Accessed June 19, 2019. https://scholarworks.gsu.edu/chemistry_theses/42.

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

MLA Handbook (7th Edition):

White, Natalie. “Optimization of Expression and Purification Methods for the Study of Protein-Based Magnetic Resonance Imaging Contrast Agents.” 2011. Web. 19 Jun 2019.

Vancouver:

White N. Optimization of Expression and Purification Methods for the Study of Protein-Based Magnetic Resonance Imaging Contrast Agents. [Internet] [Thesis]. Georgia State University; 2011. [cited 2019 Jun 19]. Available from: https://scholarworks.gsu.edu/chemistry_theses/42.

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

Council of Science Editors:

White N. Optimization of Expression and Purification Methods for the Study of Protein-Based Magnetic Resonance Imaging Contrast Agents. [Thesis]. Georgia State University; 2011. Available from: https://scholarworks.gsu.edu/chemistry_theses/42

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


Georgia State University

11. Pradhan, Devaleena. The role of social and endocrinological context in regulating life history transitions among reproductive phenotypes in in the bluebanded goby, Lythrypnus dalli.

Degree: PhD, Biology, 2014, Georgia State University

  During the lifetime of an organism, key events are orchestrated by a confluence of environmental, social, and physiological factors to promote reproductive success. Steroid… (more)

Subjects/Keywords: androgen; challenge hypothesis; courtship; fitness; parenting

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APA (6th Edition):

Pradhan, D. (2014). The role of social and endocrinological context in regulating life history transitions among reproductive phenotypes in in the bluebanded goby, Lythrypnus dalli. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/biology_diss/144

Chicago Manual of Style (16th Edition):

Pradhan, Devaleena. “The role of social and endocrinological context in regulating life history transitions among reproductive phenotypes in in the bluebanded goby, Lythrypnus dalli.” 2014. Doctoral Dissertation, Georgia State University. Accessed June 19, 2019. https://scholarworks.gsu.edu/biology_diss/144.

MLA Handbook (7th Edition):

Pradhan, Devaleena. “The role of social and endocrinological context in regulating life history transitions among reproductive phenotypes in in the bluebanded goby, Lythrypnus dalli.” 2014. Web. 19 Jun 2019.

Vancouver:

Pradhan D. The role of social and endocrinological context in regulating life history transitions among reproductive phenotypes in in the bluebanded goby, Lythrypnus dalli. [Internet] [Doctoral dissertation]. Georgia State University; 2014. [cited 2019 Jun 19]. Available from: https://scholarworks.gsu.edu/biology_diss/144.

Council of Science Editors:

Pradhan D. The role of social and endocrinological context in regulating life history transitions among reproductive phenotypes in in the bluebanded goby, Lythrypnus dalli. [Doctoral Dissertation]. Georgia State University; 2014. Available from: https://scholarworks.gsu.edu/biology_diss/144

12. Pradhan, Devaleena S. The role of social and endocrinological context in regulating life history transitions among reproductive phenotypes in the bluebanded goby, Lythrypnus dalli.

Degree: PhD, Biology, 2014, Georgia State University

  During the lifetime of an organism, key events are orchestrated by a confluence of environmental, social, and physiological factors to promote reproductive success. Steroid… (more)

Subjects/Keywords: androgen; challenge hypothesis; courtship; fitness; parenting

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APA (6th Edition):

Pradhan, D. S. (2014). The role of social and endocrinological context in regulating life history transitions among reproductive phenotypes in the bluebanded goby, Lythrypnus dalli. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/biology_diss/149

Chicago Manual of Style (16th Edition):

Pradhan, Devaleena S. “The role of social and endocrinological context in regulating life history transitions among reproductive phenotypes in the bluebanded goby, Lythrypnus dalli.” 2014. Doctoral Dissertation, Georgia State University. Accessed June 19, 2019. https://scholarworks.gsu.edu/biology_diss/149.

MLA Handbook (7th Edition):

Pradhan, Devaleena S. “The role of social and endocrinological context in regulating life history transitions among reproductive phenotypes in the bluebanded goby, Lythrypnus dalli.” 2014. Web. 19 Jun 2019.

Vancouver:

Pradhan DS. The role of social and endocrinological context in regulating life history transitions among reproductive phenotypes in the bluebanded goby, Lythrypnus dalli. [Internet] [Doctoral dissertation]. Georgia State University; 2014. [cited 2019 Jun 19]. Available from: https://scholarworks.gsu.edu/biology_diss/149.

Council of Science Editors:

Pradhan DS. The role of social and endocrinological context in regulating life history transitions among reproductive phenotypes in the bluebanded goby, Lythrypnus dalli. [Doctoral Dissertation]. Georgia State University; 2014. Available from: https://scholarworks.gsu.edu/biology_diss/149

13. Burroughs, Sarah. Design and Synthesis of HIF-1 Inhibitors as Anti-cancer Therapeutics.

Degree: PhD, Chemistry, 2013, Georgia State University

  Cancer is responsible for one fourth of the total deaths and is the second leading cause of death, behind heart disease, in the United… (more)

Subjects/Keywords: Small-molecule inhibitors; HIF; Hypoxia; Anti-cancer therapeutics; Medicinal chemistry

Giovanni Gadda, who helped me navigate the intricacies of committees and service to the… …I was prepared; Dr. Keith Pascoe, who taught me many tricks of the trade in teaching; Dr… 

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APA (6th Edition):

Burroughs, S. (2013). Design and Synthesis of HIF-1 Inhibitors as Anti-cancer Therapeutics. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_diss/78

Chicago Manual of Style (16th Edition):

Burroughs, Sarah. “Design and Synthesis of HIF-1 Inhibitors as Anti-cancer Therapeutics.” 2013. Doctoral Dissertation, Georgia State University. Accessed June 19, 2019. https://scholarworks.gsu.edu/chemistry_diss/78.

MLA Handbook (7th Edition):

Burroughs, Sarah. “Design and Synthesis of HIF-1 Inhibitors as Anti-cancer Therapeutics.” 2013. Web. 19 Jun 2019.

Vancouver:

Burroughs S. Design and Synthesis of HIF-1 Inhibitors as Anti-cancer Therapeutics. [Internet] [Doctoral dissertation]. Georgia State University; 2013. [cited 2019 Jun 19]. Available from: https://scholarworks.gsu.edu/chemistry_diss/78.

Council of Science Editors:

Burroughs S. Design and Synthesis of HIF-1 Inhibitors as Anti-cancer Therapeutics. [Doctoral Dissertation]. Georgia State University; 2013. Available from: https://scholarworks.gsu.edu/chemistry_diss/78

14. McGowan, Lauren. Using Molecular Dynamics to Elucidate the Mechanism of Cyclophilin.

Degree: PhD, Chemistry, 2014, Georgia State University

  Cyclophilins are ubiquitous enzymes that are involved in protein folding, signal transduction, viral proliferation, oncogenesis, and regulation of the immune system. Cyclophilin A is… (more)

Subjects/Keywords: Proline cis/trans isomerization; Cyclophilin A; Cyclophilin B; Enzyme catalysis; Enzyme dynamics; Enzyme isoforms

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APA (6th Edition):

McGowan, L. (2014). Using Molecular Dynamics to Elucidate the Mechanism of Cyclophilin. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_diss/88

Chicago Manual of Style (16th Edition):

McGowan, Lauren. “Using Molecular Dynamics to Elucidate the Mechanism of Cyclophilin.” 2014. Doctoral Dissertation, Georgia State University. Accessed June 19, 2019. https://scholarworks.gsu.edu/chemistry_diss/88.

MLA Handbook (7th Edition):

McGowan, Lauren. “Using Molecular Dynamics to Elucidate the Mechanism of Cyclophilin.” 2014. Web. 19 Jun 2019.

Vancouver:

McGowan L. Using Molecular Dynamics to Elucidate the Mechanism of Cyclophilin. [Internet] [Doctoral dissertation]. Georgia State University; 2014. [cited 2019 Jun 19]. Available from: https://scholarworks.gsu.edu/chemistry_diss/88.

Council of Science Editors:

McGowan L. Using Molecular Dynamics to Elucidate the Mechanism of Cyclophilin. [Doctoral Dissertation]. Georgia State University; 2014. Available from: https://scholarworks.gsu.edu/chemistry_diss/88


Georgia State University

15. Mijatovic, Slavica. Biochemical Characterization of 2-Nitropropane Dioxygenase from Hansenula MRAKII.

Degree: MS, Chemistry, 2008, Georgia State University

 2-Nitropropane dioxygenase from Hansenula mrakii is a flavin-dependent enzyme that catalyzes the oxidation of anionic nitroalkanes into the corresponding carbonyl compounds and nitrite, with oxygen… (more)

Subjects/Keywords: 2-Nitropropane Dioxygenase; Nitronate; Sulfite; Flavoprotein; FMN; Enzyme kinetics; Flavin semiquinone; Hansenula mrakii.

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APA (6th Edition):

Mijatovic, S. (2008). Biochemical Characterization of 2-Nitropropane Dioxygenase from Hansenula MRAKII. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_theses/8

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

Chicago Manual of Style (16th Edition):

Mijatovic, Slavica. “Biochemical Characterization of 2-Nitropropane Dioxygenase from Hansenula MRAKII.” 2008. Thesis, Georgia State University. Accessed June 19, 2019. https://scholarworks.gsu.edu/chemistry_theses/8.

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

MLA Handbook (7th Edition):

Mijatovic, Slavica. “Biochemical Characterization of 2-Nitropropane Dioxygenase from Hansenula MRAKII.” 2008. Web. 19 Jun 2019.

Vancouver:

Mijatovic S. Biochemical Characterization of 2-Nitropropane Dioxygenase from Hansenula MRAKII. [Internet] [Thesis]. Georgia State University; 2008. [cited 2019 Jun 19]. Available from: https://scholarworks.gsu.edu/chemistry_theses/8.

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

Council of Science Editors:

Mijatovic S. Biochemical Characterization of 2-Nitropropane Dioxygenase from Hansenula MRAKII. [Thesis]. Georgia State University; 2008. Available from: https://scholarworks.gsu.edu/chemistry_theses/8

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


Georgia State University

16. Tie, Yunfeng. Crystallographic Analysis and Kinetic Studies of HIV-1 Protease and Drug-Resistant Mutants.

Degree: PhD, Chemistry, 2006, Georgia State University

 HIV-1 protease is the most effective target for drugs to treat AIDS, however, the long-term therapeutic efficiency is restricted by the rapid development of drug… (more)

Subjects/Keywords: saquinavir; UIC-94017; substrate analog; I50V; D30N; V82A; I84V; drug resistance; HIV-1 protease; TMC-114; kinetics; crystal structure; Chemistry

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

APA (6th Edition):

Tie, Y. (2006). Crystallographic Analysis and Kinetic Studies of HIV-1 Protease and Drug-Resistant Mutants. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_diss/2

Chicago Manual of Style (16th Edition):

Tie, Yunfeng. “Crystallographic Analysis and Kinetic Studies of HIV-1 Protease and Drug-Resistant Mutants.” 2006. Doctoral Dissertation, Georgia State University. Accessed June 19, 2019. https://scholarworks.gsu.edu/chemistry_diss/2.

MLA Handbook (7th Edition):

Tie, Yunfeng. “Crystallographic Analysis and Kinetic Studies of HIV-1 Protease and Drug-Resistant Mutants.” 2006. Web. 19 Jun 2019.

Vancouver:

Tie Y. Crystallographic Analysis and Kinetic Studies of HIV-1 Protease and Drug-Resistant Mutants. [Internet] [Doctoral dissertation]. Georgia State University; 2006. [cited 2019 Jun 19]. Available from: https://scholarworks.gsu.edu/chemistry_diss/2.

Council of Science Editors:

Tie Y. Crystallographic Analysis and Kinetic Studies of HIV-1 Protease and Drug-Resistant Mutants. [Doctoral Dissertation]. Georgia State University; 2006. Available from: https://scholarworks.gsu.edu/chemistry_diss/2


Georgia State University

17. Jones, Lisa Michelle. Using Protein Design to Understand the Role of Electrostatic Interactions on Calcium Binding Affinity and Molecular Recognition.

Degree: PhD, Chemistry, 2008, Georgia State University

 Calcium regulates many biological processes through interaction with proteins with different conformational, dynamic, and metal binding properties. Previous studies have shown that the electrostatic environment… (more)

Subjects/Keywords: electrostatic potentials; protein design; calcium binding affinity; calcium binding proteins; protein stability; protein folding; Chemistry

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

APA (6th Edition):

Jones, L. M. (2008). Using Protein Design to Understand the Role of Electrostatic Interactions on Calcium Binding Affinity and Molecular Recognition. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_diss/16

Chicago Manual of Style (16th Edition):

Jones, Lisa Michelle. “Using Protein Design to Understand the Role of Electrostatic Interactions on Calcium Binding Affinity and Molecular Recognition.” 2008. Doctoral Dissertation, Georgia State University. Accessed June 19, 2019. https://scholarworks.gsu.edu/chemistry_diss/16.

MLA Handbook (7th Edition):

Jones, Lisa Michelle. “Using Protein Design to Understand the Role of Electrostatic Interactions on Calcium Binding Affinity and Molecular Recognition.” 2008. Web. 19 Jun 2019.

Vancouver:

Jones LM. Using Protein Design to Understand the Role of Electrostatic Interactions on Calcium Binding Affinity and Molecular Recognition. [Internet] [Doctoral dissertation]. Georgia State University; 2008. [cited 2019 Jun 19]. Available from: https://scholarworks.gsu.edu/chemistry_diss/16.

Council of Science Editors:

Jones LM. Using Protein Design to Understand the Role of Electrostatic Interactions on Calcium Binding Affinity and Molecular Recognition. [Doctoral Dissertation]. Georgia State University; 2008. Available from: https://scholarworks.gsu.edu/chemistry_diss/16

.