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You searched for +publisher:"University of Florida" +contributor:("Booth, Raymond "). Showing records 1 – 10 of 10 total matches.

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University of Florida

1. Kondabolu, Krishnakanth. In Vitro and in Vivo Pharmacology of Novel Phenylaminotetralin (PAT) Analogs at Serotonin 5-HT2 Receptors Development of Drugs for Neuropsychiatric Disorders.

Degree: PhD, Pharmaceutical Sciences - Medicinal Chemistry, 2013, University of Florida

 Novel 4-phenyl-N,N-dimethyl-1,2,3,4-tetrahydroanphthalene-2-amine(phenylaminotetrahydronaphthalin; PAT) analogssynthesized in our laboratories have been shown to specifically activate thehuman serotonin 5-HT2C receptors while acting as antagonists/inverseagonists at 5-HT2A and 5-HT2B… (more)

Subjects/Keywords: Agonists; Amino acids; Dosage; Enantiomers; Ligands; Locomotion; Phenyls; Receptors; Schizophrenia; Serotonin receptors; 5-ht2a  – 5-ht2b  – 5-ht2c  – drug-discovery  – gpcr  – pharmacology  – psychosis  – schizophrenia  – serotonin

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APA (6th Edition):

Kondabolu, K. (2013). In Vitro and in Vivo Pharmacology of Novel Phenylaminotetralin (PAT) Analogs at Serotonin 5-HT2 Receptors Development of Drugs for Neuropsychiatric Disorders. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0045235

Chicago Manual of Style (16th Edition):

Kondabolu, Krishnakanth. “In Vitro and in Vivo Pharmacology of Novel Phenylaminotetralin (PAT) Analogs at Serotonin 5-HT2 Receptors Development of Drugs for Neuropsychiatric Disorders.” 2013. Doctoral Dissertation, University of Florida. Accessed August 22, 2019. http://ufdc.ufl.edu/UFE0045235.

MLA Handbook (7th Edition):

Kondabolu, Krishnakanth. “In Vitro and in Vivo Pharmacology of Novel Phenylaminotetralin (PAT) Analogs at Serotonin 5-HT2 Receptors Development of Drugs for Neuropsychiatric Disorders.” 2013. Web. 22 Aug 2019.

Vancouver:

Kondabolu K. In Vitro and in Vivo Pharmacology of Novel Phenylaminotetralin (PAT) Analogs at Serotonin 5-HT2 Receptors Development of Drugs for Neuropsychiatric Disorders. [Internet] [Doctoral dissertation]. University of Florida; 2013. [cited 2019 Aug 22]. Available from: http://ufdc.ufl.edu/UFE0045235.

Council of Science Editors:

Kondabolu K. In Vitro and in Vivo Pharmacology of Novel Phenylaminotetralin (PAT) Analogs at Serotonin 5-HT2 Receptors Development of Drugs for Neuropsychiatric Disorders. [Doctoral Dissertation]. University of Florida; 2013. Available from: http://ufdc.ufl.edu/UFE0045235


University of Florida

2. Kasper, James M. Characterization of the Effects of Novel 5-Ht2c Receptor Agonists on Neurotransmission and Voluntary Alcohol Consumption in Rats.

Degree: PhD, Pharmaceutical Sciences - Pharmacodynamics, 2012, University of Florida

 This dissertation project studies the ability of 5-HT2C receptor modulators to alter voluntary ethanol intake and to investigate the changes in neurotransmission that accompany 5-HT2C… (more)

Subjects/Keywords: Agonists; Alcoholism; Dosage; Ethanol; Gelatins; Gels; Neurons; Rats; Receptors; Serotonin receptors; addiction  – alcoholism  – operant  – serotonin

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APA (6th Edition):

Kasper, J. M. (2012). Characterization of the Effects of Novel 5-Ht2c Receptor Agonists on Neurotransmission and Voluntary Alcohol Consumption in Rats. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0044635

Chicago Manual of Style (16th Edition):

Kasper, James M. “Characterization of the Effects of Novel 5-Ht2c Receptor Agonists on Neurotransmission and Voluntary Alcohol Consumption in Rats.” 2012. Doctoral Dissertation, University of Florida. Accessed August 22, 2019. http://ufdc.ufl.edu/UFE0044635.

MLA Handbook (7th Edition):

Kasper, James M. “Characterization of the Effects of Novel 5-Ht2c Receptor Agonists on Neurotransmission and Voluntary Alcohol Consumption in Rats.” 2012. Web. 22 Aug 2019.

Vancouver:

Kasper JM. Characterization of the Effects of Novel 5-Ht2c Receptor Agonists on Neurotransmission and Voluntary Alcohol Consumption in Rats. [Internet] [Doctoral dissertation]. University of Florida; 2012. [cited 2019 Aug 22]. Available from: http://ufdc.ufl.edu/UFE0044635.

Council of Science Editors:

Kasper JM. Characterization of the Effects of Novel 5-Ht2c Receptor Agonists on Neurotransmission and Voluntary Alcohol Consumption in Rats. [Doctoral Dissertation]. University of Florida; 2012. Available from: http://ufdc.ufl.edu/UFE0044635


University of Florida

3. Song, Bin. New in silico approaches for metabolic engineering.

Degree: PhD, Computer Engineering - Computer and Information Science and Engineering, 2010, University of Florida

 This thesis focuses on in silico methods for metabolic engineering. Metabolic engineering discusses methods to manipulate the metabolism to approach a given goal, e.g. increasing… (more)

Subjects/Keywords: Algorithms; Biochemical pathways; Boolean data; Datasets; Docking; Engineering; Enzymes; Genetic algorithms; Linear programming; Metabolism; genetic, heuristic, linear, metabolic

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APA (6th Edition):

Song, B. (2010). New in silico approaches for metabolic engineering. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0042323

Chicago Manual of Style (16th Edition):

Song, Bin. “New in silico approaches for metabolic engineering.” 2010. Doctoral Dissertation, University of Florida. Accessed August 22, 2019. http://ufdc.ufl.edu/UFE0042323.

MLA Handbook (7th Edition):

Song, Bin. “New in silico approaches for metabolic engineering.” 2010. Web. 22 Aug 2019.

Vancouver:

Song B. New in silico approaches for metabolic engineering. [Internet] [Doctoral dissertation]. University of Florida; 2010. [cited 2019 Aug 22]. Available from: http://ufdc.ufl.edu/UFE0042323.

Council of Science Editors:

Song B. New in silico approaches for metabolic engineering. [Doctoral Dissertation]. University of Florida; 2010. Available from: http://ufdc.ufl.edu/UFE0042323


University of Florida

4. Travers,Sean M. Characterization of the Molecular Determinants for Class A G Protein-Coupled Receptor Ligand Binding and Function Drug Discovery Targeting the Histamine H1 Receptor.

Degree: PhD, Pharmaceutical Sciences - Medicinal Chemistry, 2011, University of Florida

 This PhD thesis research project focuses on drug discovery targeting the human histamine H1 (HH1R) G protein-coupled receptor (GPCR). Certain novel phenylaminotetralin (PAT) ligands synthesized… (more)

Subjects/Keywords: Agonists; Amino acids; Dimers; Enantiomers; Histamines; Isomers; Ligands; Pendants; Phenyls; Receptors; drug  – gpcr  – h1  – histamine  – sar

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APA (6th Edition):

M, T. (2011). Characterization of the Molecular Determinants for Class A G Protein-Coupled Receptor Ligand Binding and Function Drug Discovery Targeting the Histamine H1 Receptor. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0043235

Chicago Manual of Style (16th Edition):

M, Travers,Sean. “Characterization of the Molecular Determinants for Class A G Protein-Coupled Receptor Ligand Binding and Function Drug Discovery Targeting the Histamine H1 Receptor.” 2011. Doctoral Dissertation, University of Florida. Accessed August 22, 2019. http://ufdc.ufl.edu/UFE0043235.

MLA Handbook (7th Edition):

M, Travers,Sean. “Characterization of the Molecular Determinants for Class A G Protein-Coupled Receptor Ligand Binding and Function Drug Discovery Targeting the Histamine H1 Receptor.” 2011. Web. 22 Aug 2019.

Vancouver:

M T. Characterization of the Molecular Determinants for Class A G Protein-Coupled Receptor Ligand Binding and Function Drug Discovery Targeting the Histamine H1 Receptor. [Internet] [Doctoral dissertation]. University of Florida; 2011. [cited 2019 Aug 22]. Available from: http://ufdc.ufl.edu/UFE0043235.

Council of Science Editors:

M T. Characterization of the Molecular Determinants for Class A G Protein-Coupled Receptor Ligand Binding and Function Drug Discovery Targeting the Histamine H1 Receptor. [Doctoral Dissertation]. University of Florida; 2011. Available from: http://ufdc.ufl.edu/UFE0043235


University of Florida

5. LI,WENJUN. Glutathione Transferase Z1-Catalyzed Biotransformation of Dichloroacetate - Roles of Mitochondrion, Subject Age, GSTZ1 Haplotype and Chloride Interaction.

Degree: PhD, Pharmaceutical Sciences - Medicinal Chemistry, 2011, University of Florida

 Dichloroacetate (DCA) is a potential environmental hazard and an investigational drug. By inhibiting pyruvate dehydrogenase kinase in the mitochondria, DCA remodels cellular energy metabolism and… (more)

Subjects/Keywords: Alleles; Biotransformation; Chlorides; Cytosol; Dosage; Enzymes; Haplotypes; Liver; Mitochondria; Rats; BIOTRANSFORMATION  – CHLORIDE  – DICHLOROACETATE  – GSTZ1  – MITOCHONDRIA  – POLYMORPHISM

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APA (6th Edition):

LI,WENJUN. (2011). Glutathione Transferase Z1-Catalyzed Biotransformation of Dichloroacetate - Roles of Mitochondrion, Subject Age, GSTZ1 Haplotype and Chloride Interaction. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0042766

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

LI,WENJUN. “Glutathione Transferase Z1-Catalyzed Biotransformation of Dichloroacetate - Roles of Mitochondrion, Subject Age, GSTZ1 Haplotype and Chloride Interaction.” 2011. Doctoral Dissertation, University of Florida. Accessed August 22, 2019. http://ufdc.ufl.edu/UFE0042766.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

LI,WENJUN. “Glutathione Transferase Z1-Catalyzed Biotransformation of Dichloroacetate - Roles of Mitochondrion, Subject Age, GSTZ1 Haplotype and Chloride Interaction.” 2011. Web. 22 Aug 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

LI,WENJUN. Glutathione Transferase Z1-Catalyzed Biotransformation of Dichloroacetate - Roles of Mitochondrion, Subject Age, GSTZ1 Haplotype and Chloride Interaction. [Internet] [Doctoral dissertation]. University of Florida; 2011. [cited 2019 Aug 22]. Available from: http://ufdc.ufl.edu/UFE0042766.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

LI,WENJUN. Glutathione Transferase Z1-Catalyzed Biotransformation of Dichloroacetate - Roles of Mitochondrion, Subject Age, GSTZ1 Haplotype and Chloride Interaction. [Doctoral Dissertation]. University of Florida; 2011. Available from: http://ufdc.ufl.edu/UFE0042766

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


University of Florida

6. Sun, Zhuming. Novel Phenylaminotetralin (PAT) Analogs Multifunctional Serotonin 5HT2 Receptor Drugs for Neuropsychiatric Disorders.

Degree: PhD, Pharmaceutical Sciences - Medicinal Chemistry, 2010, University of Florida

 NOVEL PHENYLAMINOTETRALIN (PAT) ANALOGS: MULTIFUNCTIONAL SEROTONIN 5HT2 RECEPTOR DRUGS FOR NEUROPSYCHIATRIC DISORDERS By Zhuming Sun August 2010 Chair: Raymond Booth Major: Pharmaceutical Science Medicinal Chemistry… (more)

Subjects/Keywords: Agonists; Amines; Antipsychotic agents; Hexanes; Isomers; Ligands; Phenyls; Receptors; Serotonin receptors; Solvents; 5ht2c, agonist, neurodisorders

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APA (6th Edition):

Sun, Z. (2010). Novel Phenylaminotetralin (PAT) Analogs Multifunctional Serotonin 5HT2 Receptor Drugs for Neuropsychiatric Disorders. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0042056

Chicago Manual of Style (16th Edition):

Sun, Zhuming. “Novel Phenylaminotetralin (PAT) Analogs Multifunctional Serotonin 5HT2 Receptor Drugs for Neuropsychiatric Disorders.” 2010. Doctoral Dissertation, University of Florida. Accessed August 22, 2019. http://ufdc.ufl.edu/UFE0042056.

MLA Handbook (7th Edition):

Sun, Zhuming. “Novel Phenylaminotetralin (PAT) Analogs Multifunctional Serotonin 5HT2 Receptor Drugs for Neuropsychiatric Disorders.” 2010. Web. 22 Aug 2019.

Vancouver:

Sun Z. Novel Phenylaminotetralin (PAT) Analogs Multifunctional Serotonin 5HT2 Receptor Drugs for Neuropsychiatric Disorders. [Internet] [Doctoral dissertation]. University of Florida; 2010. [cited 2019 Aug 22]. Available from: http://ufdc.ufl.edu/UFE0042056.

Council of Science Editors:

Sun Z. Novel Phenylaminotetralin (PAT) Analogs Multifunctional Serotonin 5HT2 Receptor Drugs for Neuropsychiatric Disorders. [Doctoral Dissertation]. University of Florida; 2010. Available from: http://ufdc.ufl.edu/UFE0042056


University of Florida

7. Park, Jongwoo. Self-Assembled Dinuclear Catalysts through Hydrogen-Bonds for Asymmetric Reactions.

Degree: PhD, Chemistry, 2011, University of Florida

 Recently, there have been growing efforts to develop multinuclear catalysts enabling cooperative, simultaneous activation of both an electrophile and a nucleophile in asymmetric catalysis. To… (more)

Subjects/Keywords: Catalysis; Catalysts; Epoxy compounds; Hydrogen; Hydrogen bonds; Kinetics; Ligands; Room temperature; Self assembly; Solvents; catalysis  – self-assembly

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APA (6th Edition):

Park, J. (2011). Self-Assembled Dinuclear Catalysts through Hydrogen-Bonds for Asymmetric Reactions. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0043184

Chicago Manual of Style (16th Edition):

Park, Jongwoo. “Self-Assembled Dinuclear Catalysts through Hydrogen-Bonds for Asymmetric Reactions.” 2011. Doctoral Dissertation, University of Florida. Accessed August 22, 2019. http://ufdc.ufl.edu/UFE0043184.

MLA Handbook (7th Edition):

Park, Jongwoo. “Self-Assembled Dinuclear Catalysts through Hydrogen-Bonds for Asymmetric Reactions.” 2011. Web. 22 Aug 2019.

Vancouver:

Park J. Self-Assembled Dinuclear Catalysts through Hydrogen-Bonds for Asymmetric Reactions. [Internet] [Doctoral dissertation]. University of Florida; 2011. [cited 2019 Aug 22]. Available from: http://ufdc.ufl.edu/UFE0043184.

Council of Science Editors:

Park J. Self-Assembled Dinuclear Catalysts through Hydrogen-Bonds for Asymmetric Reactions. [Doctoral Dissertation]. University of Florida; 2011. Available from: http://ufdc.ufl.edu/UFE0043184

8. Felsing, Daniel E. Drug Discovery Targeting Serotonin G Protein-Coupled Receptors in the Treatment of Neuropsychiatric Disorders.

Degree: PhD, Pharmaceutical Sciences - Medicinal Chemistry, 2016, University of Florida

 Clinical data show that activation of 5-HT2C G protein-coupled receptors (GPCRs) can treat obesity (lorcaserin/Belviq) and psychotic disorders (aripiprazole/Abilify), including schizophrenia. 5-HT2C GPCRs are members… (more)

Subjects/Keywords: Agonists; Canals; Inurement; Ligands; Locomotion; Medical treatment; Molecular structure; Pharmacology; Receptors; Serotonin receptors; autism  – desensitization  – psychosis  – serotonin

…Presented to the Graduate School of the University of Florida in Partial Fulfillment of the… 

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APA (6th Edition):

Felsing, D. E. (2016). Drug Discovery Targeting Serotonin G Protein-Coupled Receptors in the Treatment of Neuropsychiatric Disorders. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0049929

Chicago Manual of Style (16th Edition):

Felsing, Daniel E. “Drug Discovery Targeting Serotonin G Protein-Coupled Receptors in the Treatment of Neuropsychiatric Disorders.” 2016. Doctoral Dissertation, University of Florida. Accessed August 22, 2019. http://ufdc.ufl.edu/UFE0049929.

MLA Handbook (7th Edition):

Felsing, Daniel E. “Drug Discovery Targeting Serotonin G Protein-Coupled Receptors in the Treatment of Neuropsychiatric Disorders.” 2016. Web. 22 Aug 2019.

Vancouver:

Felsing DE. Drug Discovery Targeting Serotonin G Protein-Coupled Receptors in the Treatment of Neuropsychiatric Disorders. [Internet] [Doctoral dissertation]. University of Florida; 2016. [cited 2019 Aug 22]. Available from: http://ufdc.ufl.edu/UFE0049929.

Council of Science Editors:

Felsing DE. Drug Discovery Targeting Serotonin G Protein-Coupled Receptors in the Treatment of Neuropsychiatric Disorders. [Doctoral Dissertation]. University of Florida; 2016. Available from: http://ufdc.ufl.edu/UFE0049929


University of Florida

9. Proneth, Bettina. Rational Drug Design Approaches Targeting the Brain Melanocortin Receptors.

Degree: PhD, Pharmaceutical Sciences - Medicinal Chemistry, 2007, University of Florida

Subjects/Keywords: Agonists; Amino acids; Drug interactions; Ligands; Melanocortins; Mutagenesis; Obesity; Open reading frames; Pharmacology; Receptors; gpcr, melanocortin, mutagenesis, obesity, peptides, polymorphism, receptor, sar

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APA (6th Edition):

Proneth, B. (2007). Rational Drug Design Approaches Targeting the Brain Melanocortin Receptors. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0021556

Chicago Manual of Style (16th Edition):

Proneth, Bettina. “Rational Drug Design Approaches Targeting the Brain Melanocortin Receptors.” 2007. Doctoral Dissertation, University of Florida. Accessed August 22, 2019. http://ufdc.ufl.edu/UFE0021556.

MLA Handbook (7th Edition):

Proneth, Bettina. “Rational Drug Design Approaches Targeting the Brain Melanocortin Receptors.” 2007. Web. 22 Aug 2019.

Vancouver:

Proneth B. Rational Drug Design Approaches Targeting the Brain Melanocortin Receptors. [Internet] [Doctoral dissertation]. University of Florida; 2007. [cited 2019 Aug 22]. Available from: http://ufdc.ufl.edu/UFE0021556.

Council of Science Editors:

Proneth B. Rational Drug Design Approaches Targeting the Brain Melanocortin Receptors. [Doctoral Dissertation]. University of Florida; 2007. Available from: http://ufdc.ufl.edu/UFE0021556


University of Florida

10. Kwan, Jason. Discovery and Biological Evaluation of Secondary Metabolites from Marine Cyanobacteria.

Degree: PhD, Pharmaceutical Sciences - Medicinal Chemistry, 2010, University of Florida

Subjects/Keywords: Absorption spectra; Amino acids; Gas spectroscopy; Infrared spectrum; Magnetic resonance spectroscopy; Magnetic spectroscopy; Mass spectroscopy; Molecular spectra; Rotational spectra; Spectral correlation; bacteria, cyanobacteria, cytotoxicity, depsipeptides, nmr, peptides, proteases, virulence

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APA (6th Edition):

Kwan, J. (2010). Discovery and Biological Evaluation of Secondary Metabolites from Marine Cyanobacteria. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0042165

Chicago Manual of Style (16th Edition):

Kwan, Jason. “Discovery and Biological Evaluation of Secondary Metabolites from Marine Cyanobacteria.” 2010. Doctoral Dissertation, University of Florida. Accessed August 22, 2019. http://ufdc.ufl.edu/UFE0042165.

MLA Handbook (7th Edition):

Kwan, Jason. “Discovery and Biological Evaluation of Secondary Metabolites from Marine Cyanobacteria.” 2010. Web. 22 Aug 2019.

Vancouver:

Kwan J. Discovery and Biological Evaluation of Secondary Metabolites from Marine Cyanobacteria. [Internet] [Doctoral dissertation]. University of Florida; 2010. [cited 2019 Aug 22]. Available from: http://ufdc.ufl.edu/UFE0042165.

Council of Science Editors:

Kwan J. Discovery and Biological Evaluation of Secondary Metabolites from Marine Cyanobacteria. [Doctoral Dissertation]. University of Florida; 2010. Available from: http://ufdc.ufl.edu/UFE0042165

.