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You searched for +publisher:"Duquesne University" +contributor:("Michael Cascio"). Showing records 1 – 23 of 23 total matches.

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Duquesne University

1. Tatosian, Irena. Using Tandem Mass Spectrometry and IRMPD Spectroscopy to Determine the Intrinsic Reactions of Uranyl-Containing Ions.

Degree: MS, Chemistry and Biochemistry, 2020, Duquesne University

  Developing a comprehensive understanding of the intrinsic reactivity of uranium-containing species remains an important goal, as it may influence future developments in areas ranging… (more)

Subjects/Keywords: Tandem-Mass Spectrometry; Uranyl Ion; IRMPD Spectroscopy; CID; Analytical Chemistry; Chemistry

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APA (6th Edition):

Tatosian, I. (2020). Using Tandem Mass Spectrometry and IRMPD Spectroscopy to Determine the Intrinsic Reactions of Uranyl-Containing Ions. (Masters Thesis). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1899

Chicago Manual of Style (16th Edition):

Tatosian, Irena. “Using Tandem Mass Spectrometry and IRMPD Spectroscopy to Determine the Intrinsic Reactions of Uranyl-Containing Ions.” 2020. Masters Thesis, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/1899.

MLA Handbook (7th Edition):

Tatosian, Irena. “Using Tandem Mass Spectrometry and IRMPD Spectroscopy to Determine the Intrinsic Reactions of Uranyl-Containing Ions.” 2020. Web. 11 Apr 2021.

Vancouver:

Tatosian I. Using Tandem Mass Spectrometry and IRMPD Spectroscopy to Determine the Intrinsic Reactions of Uranyl-Containing Ions. [Internet] [Masters thesis]. Duquesne University; 2020. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/1899.

Council of Science Editors:

Tatosian I. Using Tandem Mass Spectrometry and IRMPD Spectroscopy to Determine the Intrinsic Reactions of Uranyl-Containing Ions. [Masters Thesis]. Duquesne University; 2020. Available from: https://dsc.duq.edu/etd/1899


Duquesne University

2. Veeramachaneni, Rathna Jyothi. Towards Structural Determination of Human α1-Glycine Receptor Allostery.

Degree: PhD, Chemistry and Biochemistry, 2016, Duquesne University

  Recent advances in technology have led to the determination of numerous notable structures of membrane proteins. While they provide valuable information about the structure… (more)

Subjects/Keywords: Crosslinking; GlyR; Mass Spectrometry; Membrane Proteins; Biochemistry; Chemistry

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APA (6th Edition):

Veeramachaneni, R. J. (2016). Towards Structural Determination of Human α1-Glycine Receptor Allostery. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/115

Chicago Manual of Style (16th Edition):

Veeramachaneni, Rathna Jyothi. “Towards Structural Determination of Human α1-Glycine Receptor Allostery.” 2016. Doctoral Dissertation, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/115.

MLA Handbook (7th Edition):

Veeramachaneni, Rathna Jyothi. “Towards Structural Determination of Human α1-Glycine Receptor Allostery.” 2016. Web. 11 Apr 2021.

Vancouver:

Veeramachaneni RJ. Towards Structural Determination of Human α1-Glycine Receptor Allostery. [Internet] [Doctoral dissertation]. Duquesne University; 2016. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/115.

Council of Science Editors:

Veeramachaneni RJ. Towards Structural Determination of Human α1-Glycine Receptor Allostery. [Doctoral Dissertation]. Duquesne University; 2016. Available from: https://dsc.duq.edu/etd/115


Duquesne University

3. Pope, Darrick E. Computational Modeling of the Binding of Amyloid-Beta to Neprilysin for Facilitating the Development of a Potential Alzheimer's Disease Therapy.

Degree: MS, Chemistry and Biochemistry, 2013, Duquesne University

 The zinc metalloprotease neprilysin (NEP) has been shown to degrade small bioactive peptides. Crystal structures of seven NEP-inhibitor complexes and biochemical characterization of NEP activity… (more)

Subjects/Keywords: Alzheimer's; Amyloid beta; Computer; model; Molecular dynamic; Neprilysin

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APA (6th Edition):

Pope, D. E. (2013). Computational Modeling of the Binding of Amyloid-Beta to Neprilysin for Facilitating the Development of a Potential Alzheimer's Disease Therapy. (Masters Thesis). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1507

Chicago Manual of Style (16th Edition):

Pope, Darrick E. “Computational Modeling of the Binding of Amyloid-Beta to Neprilysin for Facilitating the Development of a Potential Alzheimer's Disease Therapy.” 2013. Masters Thesis, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/1507.

MLA Handbook (7th Edition):

Pope, Darrick E. “Computational Modeling of the Binding of Amyloid-Beta to Neprilysin for Facilitating the Development of a Potential Alzheimer's Disease Therapy.” 2013. Web. 11 Apr 2021.

Vancouver:

Pope DE. Computational Modeling of the Binding of Amyloid-Beta to Neprilysin for Facilitating the Development of a Potential Alzheimer's Disease Therapy. [Internet] [Masters thesis]. Duquesne University; 2013. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/1507.

Council of Science Editors:

Pope DE. Computational Modeling of the Binding of Amyloid-Beta to Neprilysin for Facilitating the Development of a Potential Alzheimer's Disease Therapy. [Masters Thesis]. Duquesne University; 2013. Available from: https://dsc.duq.edu/etd/1507


Duquesne University

4. Stefanovic, Snezana. G Quadruplex RNA Structures in PSD-95 Mrna: Potential Regulators of Mir-125a Seed Binding Site Accessibility.

Degree: PhD, Chemistry and Biochemistry, 2015, Duquesne University

 Fragile X syndrome (FXS) is the most common inherited form of intellectual disability caused by the CGG trinucleotide expansion in the 5'-untranslated region of the… (more)

Subjects/Keywords: Pure sciences; Fmrp; Fragile x syndrome; Mir-125a; Psd-95

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APA (6th Edition):

Stefanovic, S. (2015). G Quadruplex RNA Structures in PSD-95 Mrna: Potential Regulators of Mir-125a Seed Binding Site Accessibility. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1518

Chicago Manual of Style (16th Edition):

Stefanovic, Snezana. “G Quadruplex RNA Structures in PSD-95 Mrna: Potential Regulators of Mir-125a Seed Binding Site Accessibility.” 2015. Doctoral Dissertation, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/1518.

MLA Handbook (7th Edition):

Stefanovic, Snezana. “G Quadruplex RNA Structures in PSD-95 Mrna: Potential Regulators of Mir-125a Seed Binding Site Accessibility.” 2015. Web. 11 Apr 2021.

Vancouver:

Stefanovic S. G Quadruplex RNA Structures in PSD-95 Mrna: Potential Regulators of Mir-125a Seed Binding Site Accessibility. [Internet] [Doctoral dissertation]. Duquesne University; 2015. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/1518.

Council of Science Editors:

Stefanovic S. G Quadruplex RNA Structures in PSD-95 Mrna: Potential Regulators of Mir-125a Seed Binding Site Accessibility. [Doctoral Dissertation]. Duquesne University; 2015. Available from: https://dsc.duq.edu/etd/1518


Duquesne University

5. Veeramachaneni, Rathna Jyothi. Towards Structural Determination of Human α1-Glycine Receptor Allostery.

Degree: PhD, Chemistry and Biochemistry, 2016, Duquesne University

 Recent advances in technology have led to the determination of numerous notable structures of membrane proteins. While they provide valuable information about the structure of… (more)

Subjects/Keywords: Crosslinking; GlyR; Mass Spectrometry; Membrane Proteins

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APA (6th Edition):

Veeramachaneni, R. J. (2016). Towards Structural Determination of Human α1-Glycine Receptor Allostery. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1547

Chicago Manual of Style (16th Edition):

Veeramachaneni, Rathna Jyothi. “Towards Structural Determination of Human α1-Glycine Receptor Allostery.” 2016. Doctoral Dissertation, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/1547.

MLA Handbook (7th Edition):

Veeramachaneni, Rathna Jyothi. “Towards Structural Determination of Human α1-Glycine Receptor Allostery.” 2016. Web. 11 Apr 2021.

Vancouver:

Veeramachaneni RJ. Towards Structural Determination of Human α1-Glycine Receptor Allostery. [Internet] [Doctoral dissertation]. Duquesne University; 2016. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/1547.

Council of Science Editors:

Veeramachaneni RJ. Towards Structural Determination of Human α1-Glycine Receptor Allostery. [Doctoral Dissertation]. Duquesne University; 2016. Available from: https://dsc.duq.edu/etd/1547


Duquesne University

6. Davic, Andrew Paul. Development of a Microfluidic Platform for Trace Lipid Analysis.

Degree: PhD, Chemistry and Biochemistry, 2016, Duquesne University

  The field of lipidomics encompasses the study of pathways, networks, and functionality of cellular lipids in biological systems. The lipid subclass, primary fatty acid… (more)

Subjects/Keywords: Chromatography; Fluorescence; Lab on a Chip; Laser Induced Fluorescence; Microfluidics; Primary Fatty Acid Amide

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APA (6th Edition):

Davic, A. P. (2016). Development of a Microfluidic Platform for Trace Lipid Analysis. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1516

Chicago Manual of Style (16th Edition):

Davic, Andrew Paul. “Development of a Microfluidic Platform for Trace Lipid Analysis.” 2016. Doctoral Dissertation, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/1516.

MLA Handbook (7th Edition):

Davic, Andrew Paul. “Development of a Microfluidic Platform for Trace Lipid Analysis.” 2016. Web. 11 Apr 2021.

Vancouver:

Davic AP. Development of a Microfluidic Platform for Trace Lipid Analysis. [Internet] [Doctoral dissertation]. Duquesne University; 2016. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/1516.

Council of Science Editors:

Davic AP. Development of a Microfluidic Platform for Trace Lipid Analysis. [Doctoral Dissertation]. Duquesne University; 2016. Available from: https://dsc.duq.edu/etd/1516


Duquesne University

7. Ferraro, Nicholas. State-Dependent Mapping of GlyR-Cholesterol Interactions by Coupling Crosslinking with Mass Spectrometry.

Degree: PhD, Chemistry and Biochemistry, 2019, Duquesne University

  The glycine receptor (GlyR) belongs to a superfamily of pentameric ligand-gated ion channels (pLGICs) that mediate fast neurotransmission. GlyR typically modulates inhibitory transmission by… (more)

Subjects/Keywords: Biochemistry; Biophysics; and Structural Biology

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APA (6th Edition):

Ferraro, N. (2019). State-Dependent Mapping of GlyR-Cholesterol Interactions by Coupling Crosslinking with Mass Spectrometry. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1837

Chicago Manual of Style (16th Edition):

Ferraro, Nicholas. “State-Dependent Mapping of GlyR-Cholesterol Interactions by Coupling Crosslinking with Mass Spectrometry.” 2019. Doctoral Dissertation, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/1837.

MLA Handbook (7th Edition):

Ferraro, Nicholas. “State-Dependent Mapping of GlyR-Cholesterol Interactions by Coupling Crosslinking with Mass Spectrometry.” 2019. Web. 11 Apr 2021.

Vancouver:

Ferraro N. State-Dependent Mapping of GlyR-Cholesterol Interactions by Coupling Crosslinking with Mass Spectrometry. [Internet] [Doctoral dissertation]. Duquesne University; 2019. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/1837.

Council of Science Editors:

Ferraro N. State-Dependent Mapping of GlyR-Cholesterol Interactions by Coupling Crosslinking with Mass Spectrometry. [Doctoral Dissertation]. Duquesne University; 2019. Available from: https://dsc.duq.edu/etd/1837


Duquesne University

8. Clymer, Traci M. Computational Characterization of Carboxyphosphate.

Degree: PhD, Chemistry and Biochemistry, 2015, Duquesne University

  Carboxyphosphate (CP) is an important intermediate involved in reactions catalyzed by acetyl-CoA carboxylase, pyruvate carboxylase, N5-Carboxyaminoimidazole ribonucleotide synthetase, propionyl-CoA carboxylase, urea amidolyase, and carbamoyl… (more)

Subjects/Keywords: ATP-grasp Enzymes; Biotin Carboxylase; Carboxyphosphate; Charge-assisted Hydrogen Bond; Density Functional Theory; pKa

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APA (6th Edition):

Clymer, T. M. (2015). Computational Characterization of Carboxyphosphate. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/75

Chicago Manual of Style (16th Edition):

Clymer, Traci M. “Computational Characterization of Carboxyphosphate.” 2015. Doctoral Dissertation, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/75.

MLA Handbook (7th Edition):

Clymer, Traci M. “Computational Characterization of Carboxyphosphate.” 2015. Web. 11 Apr 2021.

Vancouver:

Clymer TM. Computational Characterization of Carboxyphosphate. [Internet] [Doctoral dissertation]. Duquesne University; 2015. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/75.

Council of Science Editors:

Clymer TM. Computational Characterization of Carboxyphosphate. [Doctoral Dissertation]. Duquesne University; 2015. Available from: https://dsc.duq.edu/etd/75


Duquesne University

9. Nguyen, Bao Linh Tran. Structural Driving Factors for the Coupled Electron and Proton Transfer Reactions in Mitochondrial Cytochrome BC1 Complex: Binding Geometries of Substrates and Protonation States of Ionizable Amino Acid Side Chains Near Qi and Qo Sites.

Degree: PhD, Chemistry and Biochemistry, 2013, Duquesne University

 Coupled electron and proton transfer (CEPT) events are fundamental for many bioenergetic conversions that involve redox reactions. Understanding the details underlying CEPT processes will advance… (more)

Subjects/Keywords: Cytochrome bc1 complex; Molecular dynamics; pKa; Qi site; Qo site; Rieske Iron Sulfur Protein

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APA (6th Edition):

Nguyen, B. L. T. (2013). Structural Driving Factors for the Coupled Electron and Proton Transfer Reactions in Mitochondrial Cytochrome BC1 Complex: Binding Geometries of Substrates and Protonation States of Ionizable Amino Acid Side Chains Near Qi and Qo Sites. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/980

Chicago Manual of Style (16th Edition):

Nguyen, Bao Linh Tran. “Structural Driving Factors for the Coupled Electron and Proton Transfer Reactions in Mitochondrial Cytochrome BC1 Complex: Binding Geometries of Substrates and Protonation States of Ionizable Amino Acid Side Chains Near Qi and Qo Sites.” 2013. Doctoral Dissertation, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/980.

MLA Handbook (7th Edition):

Nguyen, Bao Linh Tran. “Structural Driving Factors for the Coupled Electron and Proton Transfer Reactions in Mitochondrial Cytochrome BC1 Complex: Binding Geometries of Substrates and Protonation States of Ionizable Amino Acid Side Chains Near Qi and Qo Sites.” 2013. Web. 11 Apr 2021.

Vancouver:

Nguyen BLT. Structural Driving Factors for the Coupled Electron and Proton Transfer Reactions in Mitochondrial Cytochrome BC1 Complex: Binding Geometries of Substrates and Protonation States of Ionizable Amino Acid Side Chains Near Qi and Qo Sites. [Internet] [Doctoral dissertation]. Duquesne University; 2013. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/980.

Council of Science Editors:

Nguyen BLT. Structural Driving Factors for the Coupled Electron and Proton Transfer Reactions in Mitochondrial Cytochrome BC1 Complex: Binding Geometries of Substrates and Protonation States of Ionizable Amino Acid Side Chains Near Qi and Qo Sites. [Doctoral Dissertation]. Duquesne University; 2013. Available from: https://dsc.duq.edu/etd/980


Duquesne University

10. Blice-Baum, Anna. Fragile X Mental Retardation Protein: Self-Regulation and miRNA Pathway Involvement.

Degree: PhD, Chemistry and Biochemistry, 2013, Duquesne University

 Fragile X syndrome, the most common form of inherited mental impairment in humans, affects 1 of 4000 males and 1 of 8000 females. It is… (more)

Subjects/Keywords: FMRP; Fragile X syndrome; G-quadruplex; mRNA

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APA (6th Edition):

Blice-Baum, A. (2013). Fragile X Mental Retardation Protein: Self-Regulation and miRNA Pathway Involvement. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/330

Chicago Manual of Style (16th Edition):

Blice-Baum, Anna. “Fragile X Mental Retardation Protein: Self-Regulation and miRNA Pathway Involvement.” 2013. Doctoral Dissertation, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/330.

MLA Handbook (7th Edition):

Blice-Baum, Anna. “Fragile X Mental Retardation Protein: Self-Regulation and miRNA Pathway Involvement.” 2013. Web. 11 Apr 2021.

Vancouver:

Blice-Baum A. Fragile X Mental Retardation Protein: Self-Regulation and miRNA Pathway Involvement. [Internet] [Doctoral dissertation]. Duquesne University; 2013. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/330.

Council of Science Editors:

Blice-Baum A. Fragile X Mental Retardation Protein: Self-Regulation and miRNA Pathway Involvement. [Doctoral Dissertation]. Duquesne University; 2013. Available from: https://dsc.duq.edu/etd/330


Duquesne University

11. Divito, Erin Blaine. Analysis Strategies for Bioactive, Polar Fatty Amides in Complex Samples.

Degree: PhD, Chemistry and Biochemistry, 2013, Duquesne University

 Bioactive lipids are known to exert physiological effects and interact with neuroreceptors. Little is known about the bioregulation of primary fatty acid amides, though N-acyl… (more)

Subjects/Keywords: bioactive lipids; fatty amides; HPLC; mass spectrometry

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APA (6th Edition):

Divito, E. B. (2013). Analysis Strategies for Bioactive, Polar Fatty Amides in Complex Samples. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/489

Chicago Manual of Style (16th Edition):

Divito, Erin Blaine. “Analysis Strategies for Bioactive, Polar Fatty Amides in Complex Samples.” 2013. Doctoral Dissertation, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/489.

MLA Handbook (7th Edition):

Divito, Erin Blaine. “Analysis Strategies for Bioactive, Polar Fatty Amides in Complex Samples.” 2013. Web. 11 Apr 2021.

Vancouver:

Divito EB. Analysis Strategies for Bioactive, Polar Fatty Amides in Complex Samples. [Internet] [Doctoral dissertation]. Duquesne University; 2013. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/489.

Council of Science Editors:

Divito EB. Analysis Strategies for Bioactive, Polar Fatty Amides in Complex Samples. [Doctoral Dissertation]. Duquesne University; 2013. Available from: https://dsc.duq.edu/etd/489


Duquesne University

12. Boggess, Andrew. Novel Solid-Phase Extraction Techniques for Biological and Environmental Analysis Using Isotope Dilution Mass Spectrometry.

Degree: PhD, Chemistry and Biochemistry, 2015, Duquesne University

 Awareness and study of the ways in which the environment can interact with the personal genetics and epigenetics of an individual has grown substantially in… (more)

Subjects/Keywords: autism; clinical chemistry; gc/ms; IDMS; mass spectrometry; SBSE

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APA (6th Edition):

Boggess, A. (2015). Novel Solid-Phase Extraction Techniques for Biological and Environmental Analysis Using Isotope Dilution Mass Spectrometry. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/332

Chicago Manual of Style (16th Edition):

Boggess, Andrew. “Novel Solid-Phase Extraction Techniques for Biological and Environmental Analysis Using Isotope Dilution Mass Spectrometry.” 2015. Doctoral Dissertation, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/332.

MLA Handbook (7th Edition):

Boggess, Andrew. “Novel Solid-Phase Extraction Techniques for Biological and Environmental Analysis Using Isotope Dilution Mass Spectrometry.” 2015. Web. 11 Apr 2021.

Vancouver:

Boggess A. Novel Solid-Phase Extraction Techniques for Biological and Environmental Analysis Using Isotope Dilution Mass Spectrometry. [Internet] [Doctoral dissertation]. Duquesne University; 2015. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/332.

Council of Science Editors:

Boggess A. Novel Solid-Phase Extraction Techniques for Biological and Environmental Analysis Using Isotope Dilution Mass Spectrometry. [Doctoral Dissertation]. Duquesne University; 2015. Available from: https://dsc.duq.edu/etd/332


Duquesne University

13. Merchant, Bonnie A. Computational techniques to illuminate secrets of the monoamine transporters.

Degree: MS, Chemistry and Biochemistry, 2012, Duquesne University

 The solute carrier family regulates the flow of various substances such as drugs, amino acids, sugars and inorganic ions across the cell membrane. In particular,… (more)

Subjects/Keywords: Biophysics; Modeling; Molecular Dynamics; Neurotransmitter; Transporters

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APA (6th Edition):

Merchant, B. A. (2012). Computational techniques to illuminate secrets of the monoamine transporters. (Masters Thesis). Duquesne University. Retrieved from https://dsc.duq.edu/etd/924

Chicago Manual of Style (16th Edition):

Merchant, Bonnie A. “Computational techniques to illuminate secrets of the monoamine transporters.” 2012. Masters Thesis, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/924.

MLA Handbook (7th Edition):

Merchant, Bonnie A. “Computational techniques to illuminate secrets of the monoamine transporters.” 2012. Web. 11 Apr 2021.

Vancouver:

Merchant BA. Computational techniques to illuminate secrets of the monoamine transporters. [Internet] [Masters thesis]. Duquesne University; 2012. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/924.

Council of Science Editors:

Merchant BA. Computational techniques to illuminate secrets of the monoamine transporters. [Masters Thesis]. Duquesne University; 2012. Available from: https://dsc.duq.edu/etd/924


Duquesne University

14. Schrott, Valerie. Characterization of the Hepatitis C Virus Genome Interactions with the microRNA miR-122: Potential New Therapeutic Targets for Peptide Nucleic Acid Based Strategies.

Degree: MS, Chemistry and Biochemistry, 2012, Duquesne University

 Hepatitis C virus (HCV), a positive-sense RNA virus that chronically infects between 2.7 and 3.9 million Americans, is highly mutational, making the HCV infection difficult… (more)

Subjects/Keywords: HCV; miR-122; PNA

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APA (6th Edition):

Schrott, V. (2012). Characterization of the Hepatitis C Virus Genome Interactions with the microRNA miR-122: Potential New Therapeutic Targets for Peptide Nucleic Acid Based Strategies. (Masters Thesis). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1157

Chicago Manual of Style (16th Edition):

Schrott, Valerie. “Characterization of the Hepatitis C Virus Genome Interactions with the microRNA miR-122: Potential New Therapeutic Targets for Peptide Nucleic Acid Based Strategies.” 2012. Masters Thesis, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/1157.

MLA Handbook (7th Edition):

Schrott, Valerie. “Characterization of the Hepatitis C Virus Genome Interactions with the microRNA miR-122: Potential New Therapeutic Targets for Peptide Nucleic Acid Based Strategies.” 2012. Web. 11 Apr 2021.

Vancouver:

Schrott V. Characterization of the Hepatitis C Virus Genome Interactions with the microRNA miR-122: Potential New Therapeutic Targets for Peptide Nucleic Acid Based Strategies. [Internet] [Masters thesis]. Duquesne University; 2012. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/1157.

Council of Science Editors:

Schrott V. Characterization of the Hepatitis C Virus Genome Interactions with the microRNA miR-122: Potential New Therapeutic Targets for Peptide Nucleic Acid Based Strategies. [Masters Thesis]. Duquesne University; 2012. Available from: https://dsc.duq.edu/etd/1157


Duquesne University

15. Patterson, Khiry L. N-terminal Imine Derivatization for Enhanced De Novo Peptide Sequencing: A Study of the Fragmentation Pattern Generated from CID of Peptide-Imines.

Degree: PhD, Chemistry and Biochemistry, 2020, Duquesne University

  In this work, the fragmentation pattern derived from model peptides derivatized to create N-terminal imines (Schiff bases) were evaluated. Collision-induced dissociation of the protonated… (more)

Subjects/Keywords: peptide fragmentation; peptidomics; gas-phase; CID; IRMPD; tandem mass spectrometry; ion trap; de novo sequencing; peptide sequencing; metal-cationized; Analytical Chemistry; Chemistry; Organic Chemistry

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APA (6th Edition):

Patterson, K. L. (2020). N-terminal Imine Derivatization for Enhanced De Novo Peptide Sequencing: A Study of the Fragmentation Pattern Generated from CID of Peptide-Imines. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1901

Chicago Manual of Style (16th Edition):

Patterson, Khiry L. “N-terminal Imine Derivatization for Enhanced De Novo Peptide Sequencing: A Study of the Fragmentation Pattern Generated from CID of Peptide-Imines.” 2020. Doctoral Dissertation, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/1901.

MLA Handbook (7th Edition):

Patterson, Khiry L. “N-terminal Imine Derivatization for Enhanced De Novo Peptide Sequencing: A Study of the Fragmentation Pattern Generated from CID of Peptide-Imines.” 2020. Web. 11 Apr 2021.

Vancouver:

Patterson KL. N-terminal Imine Derivatization for Enhanced De Novo Peptide Sequencing: A Study of the Fragmentation Pattern Generated from CID of Peptide-Imines. [Internet] [Doctoral dissertation]. Duquesne University; 2020. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/1901.

Council of Science Editors:

Patterson KL. N-terminal Imine Derivatization for Enhanced De Novo Peptide Sequencing: A Study of the Fragmentation Pattern Generated from CID of Peptide-Imines. [Doctoral Dissertation]. Duquesne University; 2020. Available from: https://dsc.duq.edu/etd/1901


Duquesne University

16. Pawlowski, Sean Christopher. Methodology for Trace and Ultratrace Analysis of Primary Amines.

Degree: PhD, Chemistry and Biochemistry, 2014, Duquesne University

 In the study of lipids, or "lipidomics," methods for the separation and identification of specific trace compounds are highly sought. Microdroplet techniques have allowed for… (more)

Subjects/Keywords: FQ; HPLC; laser induced fluorescence; LIF; microfluidics; NDA

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APA (6th Edition):

Pawlowski, S. C. (2014). Methodology for Trace and Ultratrace Analysis of Primary Amines. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1029

Chicago Manual of Style (16th Edition):

Pawlowski, Sean Christopher. “Methodology for Trace and Ultratrace Analysis of Primary Amines.” 2014. Doctoral Dissertation, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/1029.

MLA Handbook (7th Edition):

Pawlowski, Sean Christopher. “Methodology for Trace and Ultratrace Analysis of Primary Amines.” 2014. Web. 11 Apr 2021.

Vancouver:

Pawlowski SC. Methodology for Trace and Ultratrace Analysis of Primary Amines. [Internet] [Doctoral dissertation]. Duquesne University; 2014. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/1029.

Council of Science Editors:

Pawlowski SC. Methodology for Trace and Ultratrace Analysis of Primary Amines. [Doctoral Dissertation]. Duquesne University; 2014. Available from: https://dsc.duq.edu/etd/1029


Duquesne University

17. Yarravarapu, Nageswari. Monoamine Transporter Photoaffinity Ligands Based On Methylphenidate and Citalopram: Rational Design, Chemical Synthesis, and Biochemical Application.

Degree: PhD, Medicinal Chemistry, 2015, Duquesne University

 Monoamine transporters (MATs) are a family of proteins that include the dopamine transporter (DAT), serotonin transporter (SERT), and norepinephrine transporter (NET). Specifically, dysregulation of MAT… (more)

Subjects/Keywords: Pure sciences; Health and environmental sciences; Citalopram; Dopamine transporter; Methylphenidate; Monoamine transporter; Photoaffinity labeling; Serotonin transporter

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APA (6th Edition):

Yarravarapu, N. (2015). Monoamine Transporter Photoaffinity Ligands Based On Methylphenidate and Citalopram: Rational Design, Chemical Synthesis, and Biochemical Application. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1388

Chicago Manual of Style (16th Edition):

Yarravarapu, Nageswari. “Monoamine Transporter Photoaffinity Ligands Based On Methylphenidate and Citalopram: Rational Design, Chemical Synthesis, and Biochemical Application.” 2015. Doctoral Dissertation, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/1388.

MLA Handbook (7th Edition):

Yarravarapu, Nageswari. “Monoamine Transporter Photoaffinity Ligands Based On Methylphenidate and Citalopram: Rational Design, Chemical Synthesis, and Biochemical Application.” 2015. Web. 11 Apr 2021.

Vancouver:

Yarravarapu N. Monoamine Transporter Photoaffinity Ligands Based On Methylphenidate and Citalopram: Rational Design, Chemical Synthesis, and Biochemical Application. [Internet] [Doctoral dissertation]. Duquesne University; 2015. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/1388.

Council of Science Editors:

Yarravarapu N. Monoamine Transporter Photoaffinity Ligands Based On Methylphenidate and Citalopram: Rational Design, Chemical Synthesis, and Biochemical Application. [Doctoral Dissertation]. Duquesne University; 2015. Available from: https://dsc.duq.edu/etd/1388


Duquesne University

18. Anaokar, Sanket. Role of the glycerophosphocholine acyltransferase, Gpc1, in phosphatidylcholine (PC) biosynthesis and remodeling in Saccharomyces cerevisiae.

Degree: PhD, Biological Sciences, 2019, Duquesne University

  Biomembranes are permeable barriers that enclose the cell and the intracellular organelles in a cell. The selective nature of these robust barriers acts as… (more)

Subjects/Keywords: Gpc1; Ale1; phosphatidylcholine; glycerophosphocholine; lipid remodeling; acyltransferase; membrane fluidity; lipid saturation; Molecular Biology

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APA (6th Edition):

Anaokar, S. (2019). Role of the glycerophosphocholine acyltransferase, Gpc1, in phosphatidylcholine (PC) biosynthesis and remodeling in Saccharomyces cerevisiae. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1760

Chicago Manual of Style (16th Edition):

Anaokar, Sanket. “Role of the glycerophosphocholine acyltransferase, Gpc1, in phosphatidylcholine (PC) biosynthesis and remodeling in Saccharomyces cerevisiae.” 2019. Doctoral Dissertation, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/1760.

MLA Handbook (7th Edition):

Anaokar, Sanket. “Role of the glycerophosphocholine acyltransferase, Gpc1, in phosphatidylcholine (PC) biosynthesis and remodeling in Saccharomyces cerevisiae.” 2019. Web. 11 Apr 2021.

Vancouver:

Anaokar S. Role of the glycerophosphocholine acyltransferase, Gpc1, in phosphatidylcholine (PC) biosynthesis and remodeling in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. Duquesne University; 2019. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/1760.

Council of Science Editors:

Anaokar S. Role of the glycerophosphocholine acyltransferase, Gpc1, in phosphatidylcholine (PC) biosynthesis and remodeling in Saccharomyces cerevisiae. [Doctoral Dissertation]. Duquesne University; 2019. Available from: https://dsc.duq.edu/etd/1760


Duquesne University

19. Sparacino-Watkins, Courtney. Nitrate metabolism in the Epsilonproteobacteria: Campylobacter jejuni and Sulfurospirillum barnesii.

Degree: PhD, Chemistry and Biochemistry, 2011, Duquesne University

 In this study the nitrate metabolism of Campylobacter jejuni and Sulfurospirillum barnesii will be examined, specifically the periplasmic nitrate reductase (Nap) enzyme which is transforms… (more)

Subjects/Keywords: Campylobacter; Heterologous expression; Molybdenum enzymes; Nitrate reductase; Periplasmic; Protein purification

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APA (6th Edition):

Sparacino-Watkins, C. (2011). Nitrate metabolism in the Epsilonproteobacteria: Campylobacter jejuni and Sulfurospirillum barnesii. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1227

Chicago Manual of Style (16th Edition):

Sparacino-Watkins, Courtney. “Nitrate metabolism in the Epsilonproteobacteria: Campylobacter jejuni and Sulfurospirillum barnesii.” 2011. Doctoral Dissertation, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/1227.

MLA Handbook (7th Edition):

Sparacino-Watkins, Courtney. “Nitrate metabolism in the Epsilonproteobacteria: Campylobacter jejuni and Sulfurospirillum barnesii.” 2011. Web. 11 Apr 2021.

Vancouver:

Sparacino-Watkins C. Nitrate metabolism in the Epsilonproteobacteria: Campylobacter jejuni and Sulfurospirillum barnesii. [Internet] [Doctoral dissertation]. Duquesne University; 2011. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/1227.

Council of Science Editors:

Sparacino-Watkins C. Nitrate metabolism in the Epsilonproteobacteria: Campylobacter jejuni and Sulfurospirillum barnesii. [Doctoral Dissertation]. Duquesne University; 2011. Available from: https://dsc.duq.edu/etd/1227


Duquesne University

20. Thomas, John. Protein-Protein Interactions of Human Mitochondrial Amidoxime-Reducing Component in Mammalian Cells.

Degree: PhD, Chemistry and Biochemistry, 2016, Duquesne University

  Newly discovered pterin-molybdoenzymes mammalian proteins, mARC1, and mARC2, are though to activate pro-drug, metabolize mutated base pairs, and producing nitric oxide from nitrite. However,… (more)

Subjects/Keywords: mARC; Mass spectrometry; Molybdenum enzymes; Protein-protein interactions

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APA (6th Edition):

Thomas, J. (2016). Protein-Protein Interactions of Human Mitochondrial Amidoxime-Reducing Component in Mammalian Cells. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/61

Chicago Manual of Style (16th Edition):

Thomas, John. “Protein-Protein Interactions of Human Mitochondrial Amidoxime-Reducing Component in Mammalian Cells.” 2016. Doctoral Dissertation, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/61.

MLA Handbook (7th Edition):

Thomas, John. “Protein-Protein Interactions of Human Mitochondrial Amidoxime-Reducing Component in Mammalian Cells.” 2016. Web. 11 Apr 2021.

Vancouver:

Thomas J. Protein-Protein Interactions of Human Mitochondrial Amidoxime-Reducing Component in Mammalian Cells. [Internet] [Doctoral dissertation]. Duquesne University; 2016. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/61.

Council of Science Editors:

Thomas J. Protein-Protein Interactions of Human Mitochondrial Amidoxime-Reducing Component in Mammalian Cells. [Doctoral Dissertation]. Duquesne University; 2016. Available from: https://dsc.duq.edu/etd/61


Duquesne University

21. Zielen, Amanda M.C. Primate proteomic composition of seminal plasma and prostate-specific transglutaminase activity in relation to sexual selection.

Degree: PhD, Biological Sciences, 2017, Duquesne University

  Humans (Homo sapiens), chimpanzees (Pan troglodytes), and gorillas (Gorilla gorilla) have diverse mating systems with varying levels of sperm competition. Several seminal plasma genes… (more)

Subjects/Keywords: Primate; Hominid; Molecular; Evolution; Transglutaminase; Enzymatic activity; Sexual selection; Shotgun proteomics; Biochemistry; Biology; Evolution; Molecular Biology

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APA (6th Edition):

Zielen, A. M. C. (2017). Primate proteomic composition of seminal plasma and prostate-specific transglutaminase activity in relation to sexual selection. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/212

Chicago Manual of Style (16th Edition):

Zielen, Amanda M C. “Primate proteomic composition of seminal plasma and prostate-specific transglutaminase activity in relation to sexual selection.” 2017. Doctoral Dissertation, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/212.

MLA Handbook (7th Edition):

Zielen, Amanda M C. “Primate proteomic composition of seminal plasma and prostate-specific transglutaminase activity in relation to sexual selection.” 2017. Web. 11 Apr 2021.

Vancouver:

Zielen AMC. Primate proteomic composition of seminal plasma and prostate-specific transglutaminase activity in relation to sexual selection. [Internet] [Doctoral dissertation]. Duquesne University; 2017. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/212.

Council of Science Editors:

Zielen AMC. Primate proteomic composition of seminal plasma and prostate-specific transglutaminase activity in relation to sexual selection. [Doctoral Dissertation]. Duquesne University; 2017. Available from: https://dsc.duq.edu/etd/212

22. McAninch, Damian S. Neuronal GQ Structures in Neurodegeneration.

Degree: PhD, Chemistry and Biochemistry, 2017, Duquesne University

  This study investigates protein nucleic acid interactions between various proteins and G quadruplex (GQ) forming messenger RNAs (mRNAs) in human neurological disorders. GQ structures… (more)

Subjects/Keywords: ALS/FTD; Hepatitis C Virus; Fragile X Syndrom; Protein; Nucleic Acid; Biophysical Characterization; Neurodegeneration; Biochemistry; Biophysics; Structural Biology

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APA (6th Edition):

McAninch, D. S. (2017). Neuronal GQ Structures in Neurodegeneration. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/241

Chicago Manual of Style (16th Edition):

McAninch, Damian S. “Neuronal GQ Structures in Neurodegeneration.” 2017. Doctoral Dissertation, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/241.

MLA Handbook (7th Edition):

McAninch, Damian S. “Neuronal GQ Structures in Neurodegeneration.” 2017. Web. 11 Apr 2021.

Vancouver:

McAninch DS. Neuronal GQ Structures in Neurodegeneration. [Internet] [Doctoral dissertation]. Duquesne University; 2017. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/241.

Council of Science Editors:

McAninch DS. Neuronal GQ Structures in Neurodegeneration. [Doctoral Dissertation]. Duquesne University; 2017. Available from: https://dsc.duq.edu/etd/241

23. Jean, Bernandie. Modeling the Binding of Neurotransmitter Transporter Inhibitors with Molecular Dynamics and Free Energy Calculations.

Degree: PhD, Chemistry and Biochemistry, 2017, Duquesne University

  The monoamine transporter (MAT) proteins responsible for the reuptake of the neurotransmitter substrates, dopamine, serotonin, and norepinephrine, are drug targets for the treatment of… (more)

Subjects/Keywords: Molecular dynamics; Free energy perturbation; Inhibitor-stabilized conformation; Neurotransmitter transporter; Dopamine; Serotonin; Cocaine; Psychostimulant; Biophysics; Other Biochemistry, Biophysics, and Structural Biology

…graduate studies. I am thankful to my dissertation committee members, Drs. Michael Cascio, and… …Philip Reeder, and Assistant Dean Dr. Phillip D. Palmer. Thank you to the Duquesne University… 

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APA (6th Edition):

Jean, B. (2017). Modeling the Binding of Neurotransmitter Transporter Inhibitors with Molecular Dynamics and Free Energy Calculations. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/240

Chicago Manual of Style (16th Edition):

Jean, Bernandie. “Modeling the Binding of Neurotransmitter Transporter Inhibitors with Molecular Dynamics and Free Energy Calculations.” 2017. Doctoral Dissertation, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/240.

MLA Handbook (7th Edition):

Jean, Bernandie. “Modeling the Binding of Neurotransmitter Transporter Inhibitors with Molecular Dynamics and Free Energy Calculations.” 2017. Web. 11 Apr 2021.

Vancouver:

Jean B. Modeling the Binding of Neurotransmitter Transporter Inhibitors with Molecular Dynamics and Free Energy Calculations. [Internet] [Doctoral dissertation]. Duquesne University; 2017. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/240.

Council of Science Editors:

Jean B. Modeling the Binding of Neurotransmitter Transporter Inhibitors with Molecular Dynamics and Free Energy Calculations. [Doctoral Dissertation]. Duquesne University; 2017. Available from: https://dsc.duq.edu/etd/240

.