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You searched for +publisher:"Vanderbilt University" +contributor:("H. Alex Brown"). Showing records 1 – 18 of 18 total matches.

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Vanderbilt University

1. Selvy, Paige Elizabeth. Mechanistic characterization of isoform selective inhibitors of mammalian phospholipase D.

Degree: PhD, Pharmacology, 2011, Vanderbilt University

 Increasing evidence supports an integral role for the lipid second messenger phosphatidic acid (PtdOH) in cell signaling. In addition to altering curvature of biological membranes,… (more)

Subjects/Keywords: small molecule inhibitor; phospholipase D; mechanism; interfacial kinetics; enzyme kinetics; lipids

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APA (6th Edition):

Selvy, P. E. (2011). Mechanistic characterization of isoform selective inhibitors of mammalian phospholipase D. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14456

Chicago Manual of Style (16th Edition):

Selvy, Paige Elizabeth. “Mechanistic characterization of isoform selective inhibitors of mammalian phospholipase D.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed January 22, 2021. http://hdl.handle.net/1803/14456.

MLA Handbook (7th Edition):

Selvy, Paige Elizabeth. “Mechanistic characterization of isoform selective inhibitors of mammalian phospholipase D.” 2011. Web. 22 Jan 2021.

Vancouver:

Selvy PE. Mechanistic characterization of isoform selective inhibitors of mammalian phospholipase D. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/1803/14456.

Council of Science Editors:

Selvy PE. Mechanistic characterization of isoform selective inhibitors of mammalian phospholipase D. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://hdl.handle.net/1803/14456


Vanderbilt University

2. O'Reilly, Matthew Charles. Application of Organocatalysis to the Synthesis of Chiral Morpholines, Piperazines, Aziridines, Azetidines, beta-fluoroamines, and gamma-fluoroamines; Discovery of Selective Phospholipase D Inhibitors with Optimized in vivo Properties.

Degree: PhD, Chemistry, 2014, Vanderbilt University

 My doctoral research has focused on (i) using organocatalysis to prepare enantioenriched pharmaceutically relevant scaffolds and (ii) preparing isoenzyme selective inhibitors of phospholipase D. (i)… (more)

Subjects/Keywords: piperazines; morpholines; Phospholipase D; organocatalysis; fluoroamines; aziridines; azetidines

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APA (6th Edition):

O'Reilly, M. C. (2014). Application of Organocatalysis to the Synthesis of Chiral Morpholines, Piperazines, Aziridines, Azetidines, beta-fluoroamines, and gamma-fluoroamines; Discovery of Selective Phospholipase D Inhibitors with Optimized in vivo Properties. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12701

Chicago Manual of Style (16th Edition):

O'Reilly, Matthew Charles. “Application of Organocatalysis to the Synthesis of Chiral Morpholines, Piperazines, Aziridines, Azetidines, beta-fluoroamines, and gamma-fluoroamines; Discovery of Selective Phospholipase D Inhibitors with Optimized in vivo Properties.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed January 22, 2021. http://hdl.handle.net/1803/12701.

MLA Handbook (7th Edition):

O'Reilly, Matthew Charles. “Application of Organocatalysis to the Synthesis of Chiral Morpholines, Piperazines, Aziridines, Azetidines, beta-fluoroamines, and gamma-fluoroamines; Discovery of Selective Phospholipase D Inhibitors with Optimized in vivo Properties.” 2014. Web. 22 Jan 2021.

Vancouver:

O'Reilly MC. Application of Organocatalysis to the Synthesis of Chiral Morpholines, Piperazines, Aziridines, Azetidines, beta-fluoroamines, and gamma-fluoroamines; Discovery of Selective Phospholipase D Inhibitors with Optimized in vivo Properties. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/1803/12701.

Council of Science Editors:

O'Reilly MC. Application of Organocatalysis to the Synthesis of Chiral Morpholines, Piperazines, Aziridines, Azetidines, beta-fluoroamines, and gamma-fluoroamines; Discovery of Selective Phospholipase D Inhibitors with Optimized in vivo Properties. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/12701


Vanderbilt University

3. Kliman, Michal. Advanced Structural and Spatial Analysis of Lipids Using Ion Mobility-Mass Spectrometry.

Degree: PhD, Chemistry, 2011, Vanderbilt University

 Ion mobility-mass spectrometry (IM-MS) provides rapid (μs-ms) two dimensional separations on the basis of molecular structure and mass-to-charge (m/z), respectively. Based on differences in intramolecular… (more)

Subjects/Keywords: mass spectrometry; membrane lipid; lipid analysis; digital light patterning; ion mobility; mobility separation

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APA (6th Edition):

Kliman, M. (2011). Advanced Structural and Spatial Analysis of Lipids Using Ion Mobility-Mass Spectrometry. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13375

Chicago Manual of Style (16th Edition):

Kliman, Michal. “Advanced Structural and Spatial Analysis of Lipids Using Ion Mobility-Mass Spectrometry.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed January 22, 2021. http://hdl.handle.net/1803/13375.

MLA Handbook (7th Edition):

Kliman, Michal. “Advanced Structural and Spatial Analysis of Lipids Using Ion Mobility-Mass Spectrometry.” 2011. Web. 22 Jan 2021.

Vancouver:

Kliman M. Advanced Structural and Spatial Analysis of Lipids Using Ion Mobility-Mass Spectrometry. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/1803/13375.

Council of Science Editors:

Kliman M. Advanced Structural and Spatial Analysis of Lipids Using Ion Mobility-Mass Spectrometry. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://hdl.handle.net/1803/13375


Vanderbilt University

4. Tomasiak, Thomas. Catalysis, inhibition, and signal transduction by menaquinol:fumarate oxidoreductase.

Degree: PhD, Pharmacology, 2011, Vanderbilt University

 Complex II superfamily members catalyze two separate reactions in respiration: interconversion of fumarate and succinate in the soluble milieu and interconversion of quinol and quinone… (more)

Subjects/Keywords: respiration; membrane; crystallography; enzymology

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APA (6th Edition):

Tomasiak, T. (2011). Catalysis, inhibition, and signal transduction by menaquinol:fumarate oxidoreductase. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10566

Chicago Manual of Style (16th Edition):

Tomasiak, Thomas. “Catalysis, inhibition, and signal transduction by menaquinol:fumarate oxidoreductase.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed January 22, 2021. http://hdl.handle.net/1803/10566.

MLA Handbook (7th Edition):

Tomasiak, Thomas. “Catalysis, inhibition, and signal transduction by menaquinol:fumarate oxidoreductase.” 2011. Web. 22 Jan 2021.

Vancouver:

Tomasiak T. Catalysis, inhibition, and signal transduction by menaquinol:fumarate oxidoreductase. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/1803/10566.

Council of Science Editors:

Tomasiak T. Catalysis, inhibition, and signal transduction by menaquinol:fumarate oxidoreductase. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://hdl.handle.net/1803/10566


Vanderbilt University

5. Coffa, Sergio. Non-visual arrestins bind mitogen activated protein kinases and regulate their signaling.

Degree: PhD, Pharmacology, 2011, Vanderbilt University

 Arrestins are multifunctional signaling proteins, important for the regulation of signal transduction and the trafficking of G protein-coupled receptors (GPCRs). Recently, GPCR-arrestin interactions have been… (more)

Subjects/Keywords: arrestin

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APA (6th Edition):

Coffa, S. (2011). Non-visual arrestins bind mitogen activated protein kinases and regulate their signaling. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13814

Chicago Manual of Style (16th Edition):

Coffa, Sergio. “Non-visual arrestins bind mitogen activated protein kinases and regulate their signaling.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed January 22, 2021. http://hdl.handle.net/1803/13814.

MLA Handbook (7th Edition):

Coffa, Sergio. “Non-visual arrestins bind mitogen activated protein kinases and regulate their signaling.” 2011. Web. 22 Jan 2021.

Vancouver:

Coffa S. Non-visual arrestins bind mitogen activated protein kinases and regulate their signaling. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/1803/13814.

Council of Science Editors:

Coffa S. Non-visual arrestins bind mitogen activated protein kinases and regulate their signaling. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://hdl.handle.net/1803/13814


Vanderbilt University

6. Manna, Joseph Dominick. Identification and Characterization of a Major Prostaglandin Glycerol Ester Hydrolase in Human Cancer Cells.

Degree: PhD, Chemical and Physical Biology, 2014, Vanderbilt University

 Prostaglandin glycerol esters (PG-Gs) are produced by the oxygenation of the endocannabinoid, 2-arachidonoylglycerol, by cyclooxygenase 2. Understanding the role that PG-Gs play in a biological… (more)

Subjects/Keywords: Prostaglandin Glycerol Esters; Serine hydrolases; Lysophospholipase; Endocannabinoids; Activity Based Protein Profiling

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APA (6th Edition):

Manna, J. D. (2014). Identification and Characterization of a Major Prostaglandin Glycerol Ester Hydrolase in Human Cancer Cells. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12789

Chicago Manual of Style (16th Edition):

Manna, Joseph Dominick. “Identification and Characterization of a Major Prostaglandin Glycerol Ester Hydrolase in Human Cancer Cells.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed January 22, 2021. http://hdl.handle.net/1803/12789.

MLA Handbook (7th Edition):

Manna, Joseph Dominick. “Identification and Characterization of a Major Prostaglandin Glycerol Ester Hydrolase in Human Cancer Cells.” 2014. Web. 22 Jan 2021.

Vancouver:

Manna JD. Identification and Characterization of a Major Prostaglandin Glycerol Ester Hydrolase in Human Cancer Cells. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/1803/12789.

Council of Science Editors:

Manna JD. Identification and Characterization of a Major Prostaglandin Glycerol Ester Hydrolase in Human Cancer Cells. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/12789


Vanderbilt University

7. Young, Summer Elizabeth. Modulation of thrombin receptor signaling.

Degree: PhD, Pharmacology, 2013, Vanderbilt University

 The platelet thrombin receptors Protease-activated receptor 1 (PAR1) and Protease activated receptor 4 (PAR4) stand at the intersection of coagulation and platelet activation. Thrombin receptors… (more)

Subjects/Keywords: protease-activated receptor; thrombosis; thrombin receptors

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APA (6th Edition):

Young, S. E. (2013). Modulation of thrombin receptor signaling. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14534

Chicago Manual of Style (16th Edition):

Young, Summer Elizabeth. “Modulation of thrombin receptor signaling.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed January 22, 2021. http://hdl.handle.net/1803/14534.

MLA Handbook (7th Edition):

Young, Summer Elizabeth. “Modulation of thrombin receptor signaling.” 2013. Web. 22 Jan 2021.

Vancouver:

Young SE. Modulation of thrombin receptor signaling. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/1803/14534.

Council of Science Editors:

Young SE. Modulation of thrombin receptor signaling. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://hdl.handle.net/1803/14534


Vanderbilt University

8. Beavers, William Norris. w-Alkynyl Fatty Acids: Surrogates to Study Protein Adduction by Endogenously Generated Lipid Electrophiles.

Degree: PhD, Chemistry, 2015, Vanderbilt University

 Polyunsaturated Fatty Acids (PUFAs) are oxidized both enzymatically and by autoxidation to many inflammatory signaling molecules, which have been detected in multiple disease states. Oxidized… (more)

Subjects/Keywords: lipid electrophiles; polyunsaturated fatty acid oxidation; inflammation; click chemistry; stable isotope labeling of amino acids in cell culture; protein adduction

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APA (6th Edition):

Beavers, W. N. (2015). w-Alkynyl Fatty Acids: Surrogates to Study Protein Adduction by Endogenously Generated Lipid Electrophiles. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12994

Chicago Manual of Style (16th Edition):

Beavers, William Norris. “w-Alkynyl Fatty Acids: Surrogates to Study Protein Adduction by Endogenously Generated Lipid Electrophiles.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed January 22, 2021. http://hdl.handle.net/1803/12994.

MLA Handbook (7th Edition):

Beavers, William Norris. “w-Alkynyl Fatty Acids: Surrogates to Study Protein Adduction by Endogenously Generated Lipid Electrophiles.” 2015. Web. 22 Jan 2021.

Vancouver:

Beavers WN. w-Alkynyl Fatty Acids: Surrogates to Study Protein Adduction by Endogenously Generated Lipid Electrophiles. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/1803/12994.

Council of Science Editors:

Beavers WN. w-Alkynyl Fatty Acids: Surrogates to Study Protein Adduction by Endogenously Generated Lipid Electrophiles. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://hdl.handle.net/1803/12994


Vanderbilt University

9. Hermanson, Daniel John. Substrate-selective Inhibition of Cyclooxygenase-2: Molecular Determinants, Probe Development, and In Vivo Effects.

Degree: PhD, Chemistry, 2014, Vanderbilt University

 Substrate-selective Inhibition of Cyclooxygenase-2: Molecular Determinants, Probe Development, and In Vivo Effects. Daniel John Hermanson Dissertation under the direction of Professor Lawrence J. Marnett Cyclooxygenase-2… (more)

Subjects/Keywords: pain; anxiety; cyclooxygenase-2; endocannabinoids; inflammation; NSAIDs

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APA (6th Edition):

Hermanson, D. J. (2014). Substrate-selective Inhibition of Cyclooxygenase-2: Molecular Determinants, Probe Development, and In Vivo Effects. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11000

Chicago Manual of Style (16th Edition):

Hermanson, Daniel John. “Substrate-selective Inhibition of Cyclooxygenase-2: Molecular Determinants, Probe Development, and In Vivo Effects.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed January 22, 2021. http://hdl.handle.net/1803/11000.

MLA Handbook (7th Edition):

Hermanson, Daniel John. “Substrate-selective Inhibition of Cyclooxygenase-2: Molecular Determinants, Probe Development, and In Vivo Effects.” 2014. Web. 22 Jan 2021.

Vancouver:

Hermanson DJ. Substrate-selective Inhibition of Cyclooxygenase-2: Molecular Determinants, Probe Development, and In Vivo Effects. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/1803/11000.

Council of Science Editors:

Hermanson DJ. Substrate-selective Inhibition of Cyclooxygenase-2: Molecular Determinants, Probe Development, and In Vivo Effects. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/11000


Vanderbilt University

10. Bruntz, Ronald Chase. Insights into the Molecular Mechanisms of Phospholipase D-Mediated Cancer Cell Survival.

Degree: PhD, Pharmacology, 2014, Vanderbilt University

 The production of bioactive lipids by phospholipases has long been appreciated as an important mode of cellular communication. Phospholipase D (PLD) enzymes hydrolyze phosphatidylcholine to… (more)

Subjects/Keywords: phospholipase D; phosphatidic acid; cancer; Akt; cell signaling; autophagy

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APA (6th Edition):

Bruntz, R. C. (2014). Insights into the Molecular Mechanisms of Phospholipase D-Mediated Cancer Cell Survival. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10427

Chicago Manual of Style (16th Edition):

Bruntz, Ronald Chase. “Insights into the Molecular Mechanisms of Phospholipase D-Mediated Cancer Cell Survival.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed January 22, 2021. http://hdl.handle.net/1803/10427.

MLA Handbook (7th Edition):

Bruntz, Ronald Chase. “Insights into the Molecular Mechanisms of Phospholipase D-Mediated Cancer Cell Survival.” 2014. Web. 22 Jan 2021.

Vancouver:

Bruntz RC. Insights into the Molecular Mechanisms of Phospholipase D-Mediated Cancer Cell Survival. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/1803/10427.

Council of Science Editors:

Bruntz RC. Insights into the Molecular Mechanisms of Phospholipase D-Mediated Cancer Cell Survival. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/10427


Vanderbilt University

11. Lavieri, Robert Raymond. Synthesis, development and biochemical characterization of small molecule, isoform-selective phospholipase D inhibitors and photoactivatable probes.

Degree: PhD, Pharmacology, 2014, Vanderbilt University

 Phospholipase D (PLD) catalyzes the production of the lipid second messenger phosphatidic acid (PtdOH). PLD expression and/or enzymatic activity are both elevated in a variety… (more)

Subjects/Keywords: inhibitors; photoprobe; Phospholipase D; halopemide

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APA (6th Edition):

Lavieri, R. R. (2014). Synthesis, development and biochemical characterization of small molecule, isoform-selective phospholipase D inhibitors and photoactivatable probes. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14434

Chicago Manual of Style (16th Edition):

Lavieri, Robert Raymond. “Synthesis, development and biochemical characterization of small molecule, isoform-selective phospholipase D inhibitors and photoactivatable probes.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed January 22, 2021. http://hdl.handle.net/1803/14434.

MLA Handbook (7th Edition):

Lavieri, Robert Raymond. “Synthesis, development and biochemical characterization of small molecule, isoform-selective phospholipase D inhibitors and photoactivatable probes.” 2014. Web. 22 Jan 2021.

Vancouver:

Lavieri RR. Synthesis, development and biochemical characterization of small molecule, isoform-selective phospholipase D inhibitors and photoactivatable probes. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/1803/14434.

Council of Science Editors:

Lavieri RR. Synthesis, development and biochemical characterization of small molecule, isoform-selective phospholipase D inhibitors and photoactivatable probes. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/14434


Vanderbilt University

12. Spencer, Cierra Tamese. Biochemical characterization of a Pseudomonas aeruginosa phospholipase D.

Degree: PhD, Pharmacology, 2015, Vanderbilt University

 Phospholipase D (PLD) is a ubiquitous enzyme found in prokaryotic and eukaryotic organisms that generates phosphatidic acid. A number of human bacterial pathogens produce PLD… (more)

Subjects/Keywords: phospholipase D; enzymology; bacterial virulence

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APA (6th Edition):

Spencer, C. T. (2015). Biochemical characterization of a Pseudomonas aeruginosa phospholipase D. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10428

Chicago Manual of Style (16th Edition):

Spencer, Cierra Tamese. “Biochemical characterization of a Pseudomonas aeruginosa phospholipase D.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed January 22, 2021. http://hdl.handle.net/1803/10428.

MLA Handbook (7th Edition):

Spencer, Cierra Tamese. “Biochemical characterization of a Pseudomonas aeruginosa phospholipase D.” 2015. Web. 22 Jan 2021.

Vancouver:

Spencer CT. Biochemical characterization of a Pseudomonas aeruginosa phospholipase D. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/1803/10428.

Council of Science Editors:

Spencer CT. Biochemical characterization of a Pseudomonas aeruginosa phospholipase D. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://hdl.handle.net/1803/10428


Vanderbilt University

13. Zeng, Xin-Xin I. Regulation of cell movements by chemokine apelin during zebrafish development.

Degree: PhD, Biological Sciences, 2008, Vanderbilt University

 Proper embryonic development requires precise cell movements, which are coordinated by multiple signaling pathways. Formation of specific organs is initiated during gastrulation when organ precursors… (more)

Subjects/Keywords: Cellular control mechanisms; Zebra danio  – Development; convergence and extension; Cell migration; lateral plate mesoderm; primordial germ cell; G-protein coupled receptor; G proteins  – Receptors; Chemokines  – Physiological effect; Mesenchyme

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APA (6th Edition):

Zeng, X. I. (2008). Regulation of cell movements by chemokine apelin during zebrafish development. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/15325

Chicago Manual of Style (16th Edition):

Zeng, Xin-Xin I. “Regulation of cell movements by chemokine apelin during zebrafish development.” 2008. Doctoral Dissertation, Vanderbilt University. Accessed January 22, 2021. http://hdl.handle.net/1803/15325.

MLA Handbook (7th Edition):

Zeng, Xin-Xin I. “Regulation of cell movements by chemokine apelin during zebrafish development.” 2008. Web. 22 Jan 2021.

Vancouver:

Zeng XI. Regulation of cell movements by chemokine apelin during zebrafish development. [Internet] [Doctoral dissertation]. Vanderbilt University; 2008. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/1803/15325.

Council of Science Editors:

Zeng XI. Regulation of cell movements by chemokine apelin during zebrafish development. [Doctoral Dissertation]. Vanderbilt University; 2008. Available from: http://hdl.handle.net/1803/15325


Vanderbilt University

14. Huang, Fude. Rolling Blackout is required for both phototransduction and synaptic transmission in Drosophila.

Degree: PhD, Biological Sciences, 2006, Vanderbilt University

 The temperature-sensitive (TS) paralyzed and blind Drosophila mutant rolling blackout (rbo) identifies a gene encoding a protein that pioneers a novel family of membrane-associated putative… (more)

Subjects/Keywords: G protein-coupled; temperature sensitive paralysis; giant fiber; Neural transmission  – Regulation; Synapses; Photoreceptors; Drosophila  – Molecular genetics

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APA (6th Edition):

Huang, F. (2006). Rolling Blackout is required for both phototransduction and synaptic transmission in Drosophila. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11726

Chicago Manual of Style (16th Edition):

Huang, Fude. “Rolling Blackout is required for both phototransduction and synaptic transmission in Drosophila.” 2006. Doctoral Dissertation, Vanderbilt University. Accessed January 22, 2021. http://hdl.handle.net/1803/11726.

MLA Handbook (7th Edition):

Huang, Fude. “Rolling Blackout is required for both phototransduction and synaptic transmission in Drosophila.” 2006. Web. 22 Jan 2021.

Vancouver:

Huang F. Rolling Blackout is required for both phototransduction and synaptic transmission in Drosophila. [Internet] [Doctoral dissertation]. Vanderbilt University; 2006. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/1803/11726.

Council of Science Editors:

Huang F. Rolling Blackout is required for both phototransduction and synaptic transmission in Drosophila. [Doctoral Dissertation]. Vanderbilt University; 2006. Available from: http://hdl.handle.net/1803/11726


Vanderbilt University

15. Yu, Zheyong. Discovery of a novel lipoxygenase pathway in skin.

Degree: PhD, Pharmacology, 2005, Vanderbilt University

 Lipoxygenase (LOX) are non-heme iron dioxygenases that form fatty acid hydroperoxides used in membrane remodeling and cell signaling. Mammalian epidermal LOX type 3 (eLOX3) is… (more)

Subjects/Keywords: lipoxygenase; ichthyosis; skin; epoxyalcohol; hepoxilin; PPAR

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APA (6th Edition):

Yu, Z. (2005). Discovery of a novel lipoxygenase pathway in skin. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14334

Chicago Manual of Style (16th Edition):

Yu, Zheyong. “Discovery of a novel lipoxygenase pathway in skin.” 2005. Doctoral Dissertation, Vanderbilt University. Accessed January 22, 2021. http://hdl.handle.net/1803/14334.

MLA Handbook (7th Edition):

Yu, Zheyong. “Discovery of a novel lipoxygenase pathway in skin.” 2005. Web. 22 Jan 2021.

Vancouver:

Yu Z. Discovery of a novel lipoxygenase pathway in skin. [Internet] [Doctoral dissertation]. Vanderbilt University; 2005. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/1803/14334.

Council of Science Editors:

Yu Z. Discovery of a novel lipoxygenase pathway in skin. [Doctoral Dissertation]. Vanderbilt University; 2005. Available from: http://hdl.handle.net/1803/14334


Vanderbilt University

16. Jernigan, Kristin Kalie. Role of LRP6 in the Wnt/beta-catenin pathway and its regulation by heterotrimeric G proteins.

Degree: PhD, Cell and Developmental Biology, 2010, Vanderbilt University

 The Wnt/beta-catenin signaling pathway is a well-conserved signal transduction pathway that is highly regulated during metazoan development and is associated with various human diseases. In… (more)

Subjects/Keywords: LRP6; G protein signaling; wnt signaling; beta-catenin

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APA (6th Edition):

Jernigan, K. K. (2010). Role of LRP6 in the Wnt/beta-catenin pathway and its regulation by heterotrimeric G proteins. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10653

Chicago Manual of Style (16th Edition):

Jernigan, Kristin Kalie. “Role of LRP6 in the Wnt/beta-catenin pathway and its regulation by heterotrimeric G proteins.” 2010. Doctoral Dissertation, Vanderbilt University. Accessed January 22, 2021. http://hdl.handle.net/1803/10653.

MLA Handbook (7th Edition):

Jernigan, Kristin Kalie. “Role of LRP6 in the Wnt/beta-catenin pathway and its regulation by heterotrimeric G proteins.” 2010. Web. 22 Jan 2021.

Vancouver:

Jernigan KK. Role of LRP6 in the Wnt/beta-catenin pathway and its regulation by heterotrimeric G proteins. [Internet] [Doctoral dissertation]. Vanderbilt University; 2010. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/1803/10653.

Council of Science Editors:

Jernigan KK. Role of LRP6 in the Wnt/beta-catenin pathway and its regulation by heterotrimeric G proteins. [Doctoral Dissertation]. Vanderbilt University; 2010. Available from: http://hdl.handle.net/1803/10653


Vanderbilt University

17. Burnum, Kristin Elizabeth. Detecting spatial and temporal distributions of lipids and proteins during embryo implantation by MALDI Imaging Mass Spectrometry.

Degree: PhD, Biochemistry, 2008, Vanderbilt University

 Molecular events involved in successful embryo implantation take place in defined time and space but are not generally well understood. Here for the first time,… (more)

Subjects/Keywords: Imaging Mass Spectrometry; Embryo Implantation

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

APA (6th Edition):

Burnum, K. E. (2008). Detecting spatial and temporal distributions of lipids and proteins during embryo implantation by MALDI Imaging Mass Spectrometry. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/15001

Chicago Manual of Style (16th Edition):

Burnum, Kristin Elizabeth. “Detecting spatial and temporal distributions of lipids and proteins during embryo implantation by MALDI Imaging Mass Spectrometry.” 2008. Doctoral Dissertation, Vanderbilt University. Accessed January 22, 2021. http://hdl.handle.net/1803/15001.

MLA Handbook (7th Edition):

Burnum, Kristin Elizabeth. “Detecting spatial and temporal distributions of lipids and proteins during embryo implantation by MALDI Imaging Mass Spectrometry.” 2008. Web. 22 Jan 2021.

Vancouver:

Burnum KE. Detecting spatial and temporal distributions of lipids and proteins during embryo implantation by MALDI Imaging Mass Spectrometry. [Internet] [Doctoral dissertation]. Vanderbilt University; 2008. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/1803/15001.

Council of Science Editors:

Burnum KE. Detecting spatial and temporal distributions of lipids and proteins during embryo implantation by MALDI Imaging Mass Spectrometry. [Doctoral Dissertation]. Vanderbilt University; 2008. Available from: http://hdl.handle.net/1803/15001


Vanderbilt University

18. Henage, Lee Gardner. Kinetic analysis of phospholipase D: Allosteric modulation by monomeric GTPases, protein kinase C, and polyphosphoinositides.

Degree: PhD, Pharmacology, 2006, Vanderbilt University

 In mammalian cells, phospholipase D activity is tightly regulated by diverse cellular signals including hormones, neurotransmitters, and growth factors. Multiple signaling pathways converge upon phospholipase… (more)

Subjects/Keywords: phospholipase d; enzymology; G-protein; protein kinase C; ADP-ribosylation factor

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

APA (6th Edition):

Henage, L. G. (2006). Kinetic analysis of phospholipase D: Allosteric modulation by monomeric GTPases, protein kinase C, and polyphosphoinositides. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10502

Chicago Manual of Style (16th Edition):

Henage, Lee Gardner. “Kinetic analysis of phospholipase D: Allosteric modulation by monomeric GTPases, protein kinase C, and polyphosphoinositides.” 2006. Doctoral Dissertation, Vanderbilt University. Accessed January 22, 2021. http://hdl.handle.net/1803/10502.

MLA Handbook (7th Edition):

Henage, Lee Gardner. “Kinetic analysis of phospholipase D: Allosteric modulation by monomeric GTPases, protein kinase C, and polyphosphoinositides.” 2006. Web. 22 Jan 2021.

Vancouver:

Henage LG. Kinetic analysis of phospholipase D: Allosteric modulation by monomeric GTPases, protein kinase C, and polyphosphoinositides. [Internet] [Doctoral dissertation]. Vanderbilt University; 2006. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/1803/10502.

Council of Science Editors:

Henage LG. Kinetic analysis of phospholipase D: Allosteric modulation by monomeric GTPases, protein kinase C, and polyphosphoinositides. [Doctoral Dissertation]. Vanderbilt University; 2006. Available from: http://hdl.handle.net/1803/10502

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