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You searched for +publisher:"Georgia Tech" +contributor:("Sheldon W. May"). Showing records 1 – 13 of 13 total matches.

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Georgia Tech

1. Oldham, Charlie Daniel. Mechanistic studies on protocatechuate 3, 4-dioxygenase.

Degree: PhD, Chemistry, 1983, Georgia Tech

Subjects/Keywords: Oxygenases

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APA (6th Edition):

Oldham, C. D. (1983). Mechanistic studies on protocatechuate 3, 4-dioxygenase. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/29989

Chicago Manual of Style (16th Edition):

Oldham, Charlie Daniel. “Mechanistic studies on protocatechuate 3, 4-dioxygenase.” 1983. Doctoral Dissertation, Georgia Tech. Accessed March 05, 2021. http://hdl.handle.net/1853/29989.

MLA Handbook (7th Edition):

Oldham, Charlie Daniel. “Mechanistic studies on protocatechuate 3, 4-dioxygenase.” 1983. Web. 05 Mar 2021.

Vancouver:

Oldham CD. Mechanistic studies on protocatechuate 3, 4-dioxygenase. [Internet] [Doctoral dissertation]. Georgia Tech; 1983. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1853/29989.

Council of Science Editors:

Oldham CD. Mechanistic studies on protocatechuate 3, 4-dioxygenase. [Doctoral Dissertation]. Georgia Tech; 1983. Available from: http://hdl.handle.net/1853/29989


Georgia Tech

2. Ping, Dongsheng. Peptidylamidoglycolate lyase : discovery and characterization.

Degree: PhD, Chemistry and biochemistry, 1994, Georgia Tech

Subjects/Keywords: Peptides

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APA (6th Edition):

Ping, D. (1994). Peptidylamidoglycolate lyase : discovery and characterization. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/30012

Chicago Manual of Style (16th Edition):

Ping, Dongsheng. “Peptidylamidoglycolate lyase : discovery and characterization.” 1994. Doctoral Dissertation, Georgia Tech. Accessed March 05, 2021. http://hdl.handle.net/1853/30012.

MLA Handbook (7th Edition):

Ping, Dongsheng. “Peptidylamidoglycolate lyase : discovery and characterization.” 1994. Web. 05 Mar 2021.

Vancouver:

Ping D. Peptidylamidoglycolate lyase : discovery and characterization. [Internet] [Doctoral dissertation]. Georgia Tech; 1994. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1853/30012.

Council of Science Editors:

Ping D. Peptidylamidoglycolate lyase : discovery and characterization. [Doctoral Dissertation]. Georgia Tech; 1994. Available from: http://hdl.handle.net/1853/30012


Georgia Tech

3. Edwards, Alise Sarah. An investigation of the in vivo effects of DBM effectors on endogenous cathecholamine metabolism.

Degree: MS, Chemistry, 1987, Georgia Tech

Subjects/Keywords: Sympathomimetic agents

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APA (6th Edition):

Edwards, A. S. (1987). An investigation of the in vivo effects of DBM effectors on endogenous cathecholamine metabolism. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/30043

Chicago Manual of Style (16th Edition):

Edwards, Alise Sarah. “An investigation of the in vivo effects of DBM effectors on endogenous cathecholamine metabolism.” 1987. Masters Thesis, Georgia Tech. Accessed March 05, 2021. http://hdl.handle.net/1853/30043.

MLA Handbook (7th Edition):

Edwards, Alise Sarah. “An investigation of the in vivo effects of DBM effectors on endogenous cathecholamine metabolism.” 1987. Web. 05 Mar 2021.

Vancouver:

Edwards AS. An investigation of the in vivo effects of DBM effectors on endogenous cathecholamine metabolism. [Internet] [Masters thesis]. Georgia Tech; 1987. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1853/30043.

Council of Science Editors:

Edwards AS. An investigation of the in vivo effects of DBM effectors on endogenous cathecholamine metabolism. [Masters Thesis]. Georgia Tech; 1987. Available from: http://hdl.handle.net/1853/30043


Georgia Tech

4. Feng, Jun. A kinetic investigation of recombinant xenopus laevis amidating enzymes.

Degree: PhD, Chemistry and biochemistry, 1999, Georgia Tech

Subjects/Keywords: Neuropeptides Synthesis; Peptide hormones; Enzyme inhibitors; Amides

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APA (6th Edition):

Feng, J. (1999). A kinetic investigation of recombinant xenopus laevis amidating enzymes. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/30084

Chicago Manual of Style (16th Edition):

Feng, Jun. “A kinetic investigation of recombinant xenopus laevis amidating enzymes.” 1999. Doctoral Dissertation, Georgia Tech. Accessed March 05, 2021. http://hdl.handle.net/1853/30084.

MLA Handbook (7th Edition):

Feng, Jun. “A kinetic investigation of recombinant xenopus laevis amidating enzymes.” 1999. Web. 05 Mar 2021.

Vancouver:

Feng J. A kinetic investigation of recombinant xenopus laevis amidating enzymes. [Internet] [Doctoral dissertation]. Georgia Tech; 1999. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1853/30084.

Council of Science Editors:

Feng J. A kinetic investigation of recombinant xenopus laevis amidating enzymes. [Doctoral Dissertation]. Georgia Tech; 1999. Available from: http://hdl.handle.net/1853/30084


Georgia Tech

5. Moore, Allison Leigh Burrows. An investigation of xenopus laevis skin amidating enzymes expressed in the baculovirus/insect cell system.

Degree: PhD, Chemistry and biochemistry, 1997, Georgia Tech

Subjects/Keywords: Xenopus laevis; Baculoviruses

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APA (6th Edition):

Moore, A. L. B. (1997). An investigation of xenopus laevis skin amidating enzymes expressed in the baculovirus/insect cell system. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/30727

Chicago Manual of Style (16th Edition):

Moore, Allison Leigh Burrows. “An investigation of xenopus laevis skin amidating enzymes expressed in the baculovirus/insect cell system.” 1997. Doctoral Dissertation, Georgia Tech. Accessed March 05, 2021. http://hdl.handle.net/1853/30727.

MLA Handbook (7th Edition):

Moore, Allison Leigh Burrows. “An investigation of xenopus laevis skin amidating enzymes expressed in the baculovirus/insect cell system.” 1997. Web. 05 Mar 2021.

Vancouver:

Moore ALB. An investigation of xenopus laevis skin amidating enzymes expressed in the baculovirus/insect cell system. [Internet] [Doctoral dissertation]. Georgia Tech; 1997. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1853/30727.

Council of Science Editors:

Moore ALB. An investigation of xenopus laevis skin amidating enzymes expressed in the baculovirus/insect cell system. [Doctoral Dissertation]. Georgia Tech; 1997. Available from: http://hdl.handle.net/1853/30727


Georgia Tech

6. Sirimanne, Sarath Ranjith. Syntheses and enzymatic studies of novel substrate analogs of phenylalanine hydroxylase and dopamine beta monooxygenase.

Degree: PhD, Chemistry and biochemistry, 1988, Georgia Tech

Subjects/Keywords: Dopamine; Phenylalanine; Organic compounds Synthesis

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APA (6th Edition):

Sirimanne, S. R. (1988). Syntheses and enzymatic studies of novel substrate analogs of phenylalanine hydroxylase and dopamine beta monooxygenase. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/30937

Chicago Manual of Style (16th Edition):

Sirimanne, Sarath Ranjith. “Syntheses and enzymatic studies of novel substrate analogs of phenylalanine hydroxylase and dopamine beta monooxygenase.” 1988. Doctoral Dissertation, Georgia Tech. Accessed March 05, 2021. http://hdl.handle.net/1853/30937.

MLA Handbook (7th Edition):

Sirimanne, Sarath Ranjith. “Syntheses and enzymatic studies of novel substrate analogs of phenylalanine hydroxylase and dopamine beta monooxygenase.” 1988. Web. 05 Mar 2021.

Vancouver:

Sirimanne SR. Syntheses and enzymatic studies of novel substrate analogs of phenylalanine hydroxylase and dopamine beta monooxygenase. [Internet] [Doctoral dissertation]. Georgia Tech; 1988. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1853/30937.

Council of Science Editors:

Sirimanne SR. Syntheses and enzymatic studies of novel substrate analogs of phenylalanine hydroxylase and dopamine beta monooxygenase. [Doctoral Dissertation]. Georgia Tech; 1988. Available from: http://hdl.handle.net/1853/30937


Georgia Tech

7. Tulsyan, Anurag S. Molecular cloning and characterization of a novel developmental gene from loblolly pine - a new plant regulatory system.

Degree: MS, Chemistry and biochemistry, 2001, Georgia Tech

Subjects/Keywords: Developmental genetics; Molecular cloning; Loblolly pine

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APA (6th Edition):

Tulsyan, A. S. (2001). Molecular cloning and characterization of a novel developmental gene from loblolly pine - a new plant regulatory system. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/31014

Chicago Manual of Style (16th Edition):

Tulsyan, Anurag S. “Molecular cloning and characterization of a novel developmental gene from loblolly pine - a new plant regulatory system.” 2001. Masters Thesis, Georgia Tech. Accessed March 05, 2021. http://hdl.handle.net/1853/31014.

MLA Handbook (7th Edition):

Tulsyan, Anurag S. “Molecular cloning and characterization of a novel developmental gene from loblolly pine - a new plant regulatory system.” 2001. Web. 05 Mar 2021.

Vancouver:

Tulsyan AS. Molecular cloning and characterization of a novel developmental gene from loblolly pine - a new plant regulatory system. [Internet] [Masters thesis]. Georgia Tech; 2001. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1853/31014.

Council of Science Editors:

Tulsyan AS. Molecular cloning and characterization of a novel developmental gene from loblolly pine - a new plant regulatory system. [Masters Thesis]. Georgia Tech; 2001. Available from: http://hdl.handle.net/1853/31014

8. Kosa, Matyas. Direct and multistep conversion of lignin to biofuels.

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

 Lignin is the second most abundant biopolymer on Earth, right after cellulose, with a highly complex chemical structure that hinders its possible utilizations. Applications that… (more)

Subjects/Keywords: Lignin; Lipid; Oleaginous bateria; Rhodococcus; Beta-ketoadipate; Pyrolysis; Biomass conversion; Biomass energy; Energy crops

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APA (6th Edition):

Kosa, M. (2012). Direct and multistep conversion of lignin to biofuels. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/45836

Chicago Manual of Style (16th Edition):

Kosa, Matyas. “Direct and multistep conversion of lignin to biofuels.” 2012. Doctoral Dissertation, Georgia Tech. Accessed March 05, 2021. http://hdl.handle.net/1853/45836.

MLA Handbook (7th Edition):

Kosa, Matyas. “Direct and multistep conversion of lignin to biofuels.” 2012. Web. 05 Mar 2021.

Vancouver:

Kosa M. Direct and multistep conversion of lignin to biofuels. [Internet] [Doctoral dissertation]. Georgia Tech; 2012. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1853/45836.

Council of Science Editors:

Kosa M. Direct and multistep conversion of lignin to biofuels. [Doctoral Dissertation]. Georgia Tech; 2012. Available from: http://hdl.handle.net/1853/45836

9. Ovat, Asli. Design, synthesis and evaluation of cysteine protease inhibitors.

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

 Cysteine proteases are important drug targets due to their involvement in many biological processes such as protein turnover, digestion, blood coagulation, apoptosis, cell differentiation, cell… (more)

Subjects/Keywords: Legumain; Calpain; Protease; Cysteine; Cysteine proteinases; Cysteine proteinases Inhibitors; Protease inhibitors; Biosynthesis; Epoxy compounds

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APA (6th Edition):

Ovat, A. (2009). Design, synthesis and evaluation of cysteine protease inhibitors. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/33822

Chicago Manual of Style (16th Edition):

Ovat, Asli. “Design, synthesis and evaluation of cysteine protease inhibitors.” 2009. Doctoral Dissertation, Georgia Tech. Accessed March 05, 2021. http://hdl.handle.net/1853/33822.

MLA Handbook (7th Edition):

Ovat, Asli. “Design, synthesis and evaluation of cysteine protease inhibitors.” 2009. Web. 05 Mar 2021.

Vancouver:

Ovat A. Design, synthesis and evaluation of cysteine protease inhibitors. [Internet] [Doctoral dissertation]. Georgia Tech; 2009. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1853/33822.

Council of Science Editors:

Ovat A. Design, synthesis and evaluation of cysteine protease inhibitors. [Doctoral Dissertation]. Georgia Tech; 2009. Available from: http://hdl.handle.net/1853/33822


Georgia Tech

10. Burns, Kristi Lee. An exploration of biochemistry including biotechnology, structural characterization, drug design, and chromatographic analyses.

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

 We now report an in depth analysis of the successful in vitro enzymatic synthesis of PHB utilizing the three-enzyme system from the bacteria Cupriavidus necator.… (more)

Subjects/Keywords: Iso-coa; Iso-coenzyme A; Poly-(beta)-hydroxybutyric acid; PHB; Phenylaminoethyl selenide compounds; Biopolyesters; Acetyl-iso-coa; Acetoacetyl-iso-coa; Regioselective synthesis; Homepaes; DNA; DNA damage; Single-strand breaks; Acyl-transfer reactions; Culturing; Homo-nuclear NMR; Purifying; Producing; Isolating; Isomers; Selective COX-II inhibitors; Whole blood; Structural characterizations; ELISA; In vitro; Enzymatic synthesis; Beta-hydroxybutyryl-iso-coa; MS/MS; MS; HPLC; Metabolic model; Hetero-nuclear NMR; Peroxynitrite; HPLC/MS; CDB derivatives; Poly-beta-hydroxybutyrate; Biosynthesis

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APA (6th Edition):

Burns, K. L. (2006). An exploration of biochemistry including biotechnology, structural characterization, drug design, and chromatographic analyses. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/29593

Chicago Manual of Style (16th Edition):

Burns, Kristi Lee. “An exploration of biochemistry including biotechnology, structural characterization, drug design, and chromatographic analyses.” 2006. Doctoral Dissertation, Georgia Tech. Accessed March 05, 2021. http://hdl.handle.net/1853/29593.

MLA Handbook (7th Edition):

Burns, Kristi Lee. “An exploration of biochemistry including biotechnology, structural characterization, drug design, and chromatographic analyses.” 2006. Web. 05 Mar 2021.

Vancouver:

Burns KL. An exploration of biochemistry including biotechnology, structural characterization, drug design, and chromatographic analyses. [Internet] [Doctoral dissertation]. Georgia Tech; 2006. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1853/29593.

Council of Science Editors:

Burns KL. An exploration of biochemistry including biotechnology, structural characterization, drug design, and chromatographic analyses. [Doctoral Dissertation]. Georgia Tech; 2006. Available from: http://hdl.handle.net/1853/29593


Georgia Tech

11. Chen, Yanfeng. Analysis of Biological Molecules Using Stimulated Desorption Photoionization Mass Spectrometry.

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

 Surface-assisted laser desorption/ionization mass spectrometry (SALDI MS) is a novel technique for direct analysis of organic and biological molecules. Amino acids, dipeptides, and organoselenium compounds… (more)

Subjects/Keywords: Single photon ionization; Selenium metabolites; Electron stimulated desorption; DNA damage; Surface-assisted laser desorption/ionization; Mass spectrometry

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APA (6th Edition):

Chen, Y. (2006). Analysis of Biological Molecules Using Stimulated Desorption Photoionization Mass Spectrometry. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/14620

Chicago Manual of Style (16th Edition):

Chen, Yanfeng. “Analysis of Biological Molecules Using Stimulated Desorption Photoionization Mass Spectrometry.” 2006. Doctoral Dissertation, Georgia Tech. Accessed March 05, 2021. http://hdl.handle.net/1853/14620.

MLA Handbook (7th Edition):

Chen, Yanfeng. “Analysis of Biological Molecules Using Stimulated Desorption Photoionization Mass Spectrometry.” 2006. Web. 05 Mar 2021.

Vancouver:

Chen Y. Analysis of Biological Molecules Using Stimulated Desorption Photoionization Mass Spectrometry. [Internet] [Doctoral dissertation]. Georgia Tech; 2006. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1853/14620.

Council of Science Editors:

Chen Y. Analysis of Biological Molecules Using Stimulated Desorption Photoionization Mass Spectrometry. [Doctoral Dissertation]. Georgia Tech; 2006. Available from: http://hdl.handle.net/1853/14620


Georgia Tech

12. Azizi, Bahareh. Chemical Complementation: A Genetic Selection System in Yeast for Drug Discovery, Protein Engineering, and for Deciphering and Assembling Biosynthetic Pathways.

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

 Chemical complementation is a general system for detecting protein-small molecule interactions, and linking that interaction to genetic selection. In this chemical complementation system, the interaction… (more)

Subjects/Keywords: Enzyme engineering; Chemical genetics

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APA (6th Edition):

Azizi, B. (2005). Chemical Complementation: A Genetic Selection System in Yeast for Drug Discovery, Protein Engineering, and for Deciphering and Assembling Biosynthetic Pathways. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/11637

Chicago Manual of Style (16th Edition):

Azizi, Bahareh. “Chemical Complementation: A Genetic Selection System in Yeast for Drug Discovery, Protein Engineering, and for Deciphering and Assembling Biosynthetic Pathways.” 2005. Doctoral Dissertation, Georgia Tech. Accessed March 05, 2021. http://hdl.handle.net/1853/11637.

MLA Handbook (7th Edition):

Azizi, Bahareh. “Chemical Complementation: A Genetic Selection System in Yeast for Drug Discovery, Protein Engineering, and for Deciphering and Assembling Biosynthetic Pathways.” 2005. Web. 05 Mar 2021.

Vancouver:

Azizi B. Chemical Complementation: A Genetic Selection System in Yeast for Drug Discovery, Protein Engineering, and for Deciphering and Assembling Biosynthetic Pathways. [Internet] [Doctoral dissertation]. Georgia Tech; 2005. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1853/11637.

Council of Science Editors:

Azizi B. Chemical Complementation: A Genetic Selection System in Yeast for Drug Discovery, Protein Engineering, and for Deciphering and Assembling Biosynthetic Pathways. [Doctoral Dissertation]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/11637


Georgia Tech

13. Foster, Michael Scott. Design, synthesis, kinetic analysis, molecular modeling, and pharmacological evaluation of novel inhibitors of peptide amidation.

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

 Novel, rationally-designed acrylate analogs of various known dipeptide substrates were found to be mechanism-based inactivators of the enzyme peptidylglycine alpha-amidating monooxygenase (PAM, EC 1.14.17.3). This… (more)

Subjects/Keywords: Molecular modeling; Stereochemistry; Molecules Models; Peptides; Chemical structure; Peptide hormones; Neuropeptides

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APA (6th Edition):

Foster, M. S. (2008). Design, synthesis, kinetic analysis, molecular modeling, and pharmacological evaluation of novel inhibitors of peptide amidation. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/31816

Chicago Manual of Style (16th Edition):

Foster, Michael Scott. “Design, synthesis, kinetic analysis, molecular modeling, and pharmacological evaluation of novel inhibitors of peptide amidation.” 2008. Doctoral Dissertation, Georgia Tech. Accessed March 05, 2021. http://hdl.handle.net/1853/31816.

MLA Handbook (7th Edition):

Foster, Michael Scott. “Design, synthesis, kinetic analysis, molecular modeling, and pharmacological evaluation of novel inhibitors of peptide amidation.” 2008. Web. 05 Mar 2021.

Vancouver:

Foster MS. Design, synthesis, kinetic analysis, molecular modeling, and pharmacological evaluation of novel inhibitors of peptide amidation. [Internet] [Doctoral dissertation]. Georgia Tech; 2008. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1853/31816.

Council of Science Editors:

Foster MS. Design, synthesis, kinetic analysis, molecular modeling, and pharmacological evaluation of novel inhibitors of peptide amidation. [Doctoral Dissertation]. Georgia Tech; 2008. Available from: http://hdl.handle.net/1853/31816

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