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You searched for +publisher:"Georgia Tech" +contributor:("Radhakrishna, Harish"). Showing records 1 – 13 of 13 total matches.

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1. Vincent, Karla Kristine. Transactivation of Beta 2 Adrenergic Receptor by Bradykinin type 2 Receptor via heterodimerization.

Degree: PhD, Biology, 2009, Georgia Tech

 Although a long standing convention maintained that G Protein Coupled Receptors (GPCRs) exist in the plasma membrane solely as monomers, substantial work over the last… (more)

Subjects/Keywords: Electrophysiology; Heterodimer; GPCR; G proteins; Membrane proteins

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APA (6th Edition):

Vincent, K. K. (2009). Transactivation of Beta 2 Adrenergic Receptor by Bradykinin type 2 Receptor via heterodimerization. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/37117

Chicago Manual of Style (16th Edition):

Vincent, Karla Kristine. “Transactivation of Beta 2 Adrenergic Receptor by Bradykinin type 2 Receptor via heterodimerization.” 2009. Doctoral Dissertation, Georgia Tech. Accessed January 23, 2021. http://hdl.handle.net/1853/37117.

MLA Handbook (7th Edition):

Vincent, Karla Kristine. “Transactivation of Beta 2 Adrenergic Receptor by Bradykinin type 2 Receptor via heterodimerization.” 2009. Web. 23 Jan 2021.

Vancouver:

Vincent KK. Transactivation of Beta 2 Adrenergic Receptor by Bradykinin type 2 Receptor via heterodimerization. [Internet] [Doctoral dissertation]. Georgia Tech; 2009. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/1853/37117.

Council of Science Editors:

Vincent KK. Transactivation of Beta 2 Adrenergic Receptor by Bradykinin type 2 Receptor via heterodimerization. [Doctoral Dissertation]. Georgia Tech; 2009. Available from: http://hdl.handle.net/1853/37117


Georgia Tech

2. Murph, Mandi Michelle. A characterization of the human G protein-coupled receptor, lysophosphatidic acid1 : its intracellular trafficking and signaling consequences on the tumor suppressor, P53.

Degree: PhD, Biology, 2005, Georgia Tech

 Lysophosphatidic acid (LPA) is a mitogenic lipid that enhances cell growth, proliferation and motility through binding and activation of at least four receptors, LPA1/Edg2, LPA2/Edg4,… (more)

Subjects/Keywords: LPA; G protein-coupled receptors; p53; LPA1; Lysophospholipids; Endocytosis; Cancer cells Growth

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APA (6th Edition):

Murph, M. M. (2005). A characterization of the human G protein-coupled receptor, lysophosphatidic acid1 : its intracellular trafficking and signaling consequences on the tumor suppressor, P53. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/6869

Chicago Manual of Style (16th Edition):

Murph, Mandi Michelle. “A characterization of the human G protein-coupled receptor, lysophosphatidic acid1 : its intracellular trafficking and signaling consequences on the tumor suppressor, P53.” 2005. Doctoral Dissertation, Georgia Tech. Accessed January 23, 2021. http://hdl.handle.net/1853/6869.

MLA Handbook (7th Edition):

Murph, Mandi Michelle. “A characterization of the human G protein-coupled receptor, lysophosphatidic acid1 : its intracellular trafficking and signaling consequences on the tumor suppressor, P53.” 2005. Web. 23 Jan 2021.

Vancouver:

Murph MM. A characterization of the human G protein-coupled receptor, lysophosphatidic acid1 : its intracellular trafficking and signaling consequences on the tumor suppressor, P53. [Internet] [Doctoral dissertation]. Georgia Tech; 2005. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/1853/6869.

Council of Science Editors:

Murph MM. A characterization of the human G protein-coupled receptor, lysophosphatidic acid1 : its intracellular trafficking and signaling consequences on the tumor suppressor, P53. [Doctoral Dissertation]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/6869


Georgia Tech

3. Santai, Catherine Theresa. In vitro Condensation of Mixed-Stranded DNA.

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

 DNA condensation is the process in which an anionic polymer in combination with condensing agents undergoes a drastic reduction in volume and collapses into ordered… (more)

Subjects/Keywords: Mixed-stranded; DNA; Condensation; Single-stranded; Condensation; DNA Synthesis; Addition polymerization

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APA (6th Edition):

Santai, C. T. (2006). In vitro Condensation of Mixed-Stranded DNA. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/14043

Chicago Manual of Style (16th Edition):

Santai, Catherine Theresa. “In vitro Condensation of Mixed-Stranded DNA.” 2006. Doctoral Dissertation, Georgia Tech. Accessed January 23, 2021. http://hdl.handle.net/1853/14043.

MLA Handbook (7th Edition):

Santai, Catherine Theresa. “In vitro Condensation of Mixed-Stranded DNA.” 2006. Web. 23 Jan 2021.

Vancouver:

Santai CT. In vitro Condensation of Mixed-Stranded DNA. [Internet] [Doctoral dissertation]. Georgia Tech; 2006. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/1853/14043.

Council of Science Editors:

Santai CT. In vitro Condensation of Mixed-Stranded DNA. [Doctoral Dissertation]. Georgia Tech; 2006. Available from: http://hdl.handle.net/1853/14043


Georgia Tech

4. Michael, Kristin E. FAK Modulates Cell Adhesion Strengthening Via Two Distinct Mechanisms: Integrin Binding and Vinculin Localization.

Degree: PhD, Bioengineering, 2006, Georgia Tech

 Cell adhesion to the extracellular matrix (ECM) provides tissue structure and integrity as well as triggers signals that regulate complex biological processes such as cell… (more)

Subjects/Keywords: Focal adhesion kinase; Extracellular matrix; Integrins; Cell adhesion; Cell mechanics; Force; Migration; Fibronectin; Immobilized proteins; Integrins; Cell adhesion; Extracellular matrix; Fibronectins; Focal adhesion kinase

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APA (6th Edition):

Michael, K. E. (2006). FAK Modulates Cell Adhesion Strengthening Via Two Distinct Mechanisms: Integrin Binding and Vinculin Localization. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/14136

Chicago Manual of Style (16th Edition):

Michael, Kristin E. “FAK Modulates Cell Adhesion Strengthening Via Two Distinct Mechanisms: Integrin Binding and Vinculin Localization.” 2006. Doctoral Dissertation, Georgia Tech. Accessed January 23, 2021. http://hdl.handle.net/1853/14136.

MLA Handbook (7th Edition):

Michael, Kristin E. “FAK Modulates Cell Adhesion Strengthening Via Two Distinct Mechanisms: Integrin Binding and Vinculin Localization.” 2006. Web. 23 Jan 2021.

Vancouver:

Michael KE. FAK Modulates Cell Adhesion Strengthening Via Two Distinct Mechanisms: Integrin Binding and Vinculin Localization. [Internet] [Doctoral dissertation]. Georgia Tech; 2006. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/1853/14136.

Council of Science Editors:

Michael KE. FAK Modulates Cell Adhesion Strengthening Via Two Distinct Mechanisms: Integrin Binding and Vinculin Localization. [Doctoral Dissertation]. Georgia Tech; 2006. Available from: http://hdl.handle.net/1853/14136


Georgia Tech

5. Ozbay, Tuba Selcuk. The Role of Sphingolipids in Cortisol Synthesis in the Adrenal Cortex.

Degree: MS, Biology, 2005, Georgia Tech

 In the human adrenal cortex, adrenocorticotropin (ACTH) activates steroid hormone biosynthesis by acutely increasing cholesterol delivery to the mitochondria and chronically up-regulating the transcription of… (more)

Subjects/Keywords: SREBP; S1P; CYP17; Sphingolipids; Adrenal cortex; Sphingolipids

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APA (6th Edition):

Ozbay, T. S. (2005). The Role of Sphingolipids in Cortisol Synthesis in the Adrenal Cortex. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/7549

Chicago Manual of Style (16th Edition):

Ozbay, Tuba Selcuk. “The Role of Sphingolipids in Cortisol Synthesis in the Adrenal Cortex.” 2005. Masters Thesis, Georgia Tech. Accessed January 23, 2021. http://hdl.handle.net/1853/7549.

MLA Handbook (7th Edition):

Ozbay, Tuba Selcuk. “The Role of Sphingolipids in Cortisol Synthesis in the Adrenal Cortex.” 2005. Web. 23 Jan 2021.

Vancouver:

Ozbay TS. The Role of Sphingolipids in Cortisol Synthesis in the Adrenal Cortex. [Internet] [Masters thesis]. Georgia Tech; 2005. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/1853/7549.

Council of Science Editors:

Ozbay TS. The Role of Sphingolipids in Cortisol Synthesis in the Adrenal Cortex. [Masters Thesis]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/7549


Georgia Tech

6. Gallant, Nathan D. Analysis of Integrin-mediated Cell Adhesion Strengthening Using Surfaces Engineered to Control Cell Shape and Focal Adhesion Assembly.

Degree: PhD, Mechanical Engineering, 2004, Georgia Tech

 Cell adhesion to extracellular matrix proteins is critical to physiological and pathological processes as well as biomedical and biotechnological applications. Cell adhesion is a highly… (more)

Subjects/Keywords: Biological interfaces; Cell adhesion Analysis; Cell adhesion Mechanical properties; Integrins; Micropatterning; Surface chemistry; Tissue engineering

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APA (6th Edition):

Gallant, N. D. (2004). Analysis of Integrin-mediated Cell Adhesion Strengthening Using Surfaces Engineered to Control Cell Shape and Focal Adhesion Assembly. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/7601

Chicago Manual of Style (16th Edition):

Gallant, Nathan D. “Analysis of Integrin-mediated Cell Adhesion Strengthening Using Surfaces Engineered to Control Cell Shape and Focal Adhesion Assembly.” 2004. Doctoral Dissertation, Georgia Tech. Accessed January 23, 2021. http://hdl.handle.net/1853/7601.

MLA Handbook (7th Edition):

Gallant, Nathan D. “Analysis of Integrin-mediated Cell Adhesion Strengthening Using Surfaces Engineered to Control Cell Shape and Focal Adhesion Assembly.” 2004. Web. 23 Jan 2021.

Vancouver:

Gallant ND. Analysis of Integrin-mediated Cell Adhesion Strengthening Using Surfaces Engineered to Control Cell Shape and Focal Adhesion Assembly. [Internet] [Doctoral dissertation]. Georgia Tech; 2004. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/1853/7601.

Council of Science Editors:

Gallant ND. Analysis of Integrin-mediated Cell Adhesion Strengthening Using Surfaces Engineered to Control Cell Shape and Focal Adhesion Assembly. [Doctoral Dissertation]. Georgia Tech; 2004. Available from: http://hdl.handle.net/1853/7601


Georgia Tech

7. Vanderploeg, Eric James. Mechanotransduction in Engineered Cartilaginous Tissues: In Vitro Oscillatory Tensile Loading.

Degree: PhD, Mechanical Engineering, 2006, Georgia Tech

 Disease and degeneration of articular cartilage and fibrocartilage tissues severely compromise the quality of life for millions of people. Although current surgical repair techniques can… (more)

Subjects/Keywords: Tensile loading; Mechanical stimulation; Meniscus; Tissue engineering; Fibrocartilage; Cartilage; Tissue engineering; Loads (Mechanics); Biomechanics; Articular cartilage Mechanical properties

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APA (6th Edition):

Vanderploeg, E. J. (2006). Mechanotransduction in Engineered Cartilaginous Tissues: In Vitro Oscillatory Tensile Loading. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/11483

Chicago Manual of Style (16th Edition):

Vanderploeg, Eric James. “Mechanotransduction in Engineered Cartilaginous Tissues: In Vitro Oscillatory Tensile Loading.” 2006. Doctoral Dissertation, Georgia Tech. Accessed January 23, 2021. http://hdl.handle.net/1853/11483.

MLA Handbook (7th Edition):

Vanderploeg, Eric James. “Mechanotransduction in Engineered Cartilaginous Tissues: In Vitro Oscillatory Tensile Loading.” 2006. Web. 23 Jan 2021.

Vancouver:

Vanderploeg EJ. Mechanotransduction in Engineered Cartilaginous Tissues: In Vitro Oscillatory Tensile Loading. [Internet] [Doctoral dissertation]. Georgia Tech; 2006. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/1853/11483.

Council of Science Editors:

Vanderploeg EJ. Mechanotransduction in Engineered Cartilaginous Tissues: In Vitro Oscillatory Tensile Loading. [Doctoral Dissertation]. Georgia Tech; 2006. Available from: http://hdl.handle.net/1853/11483


Georgia Tech

8. Schwimmer, Lauren J. Engineering ligand-receptor pairs for small molecule control of transcription.

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

 Creating receptors for control of transcription with arbitrary small molecules has widespread applications including gene therapy, biosensors, and enzyme engineering. Using the combination of high… (more)

Subjects/Keywords: Chemical complementation; Ligand-receptor pair; Protein engineering; Retinoid X receptor; Nuclear receptor; Codon randomized libraries; Transcription factors; Protein engineering; Nuclear receptors (Biochemistry); Genetic engineering

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APA (6th Edition):

Schwimmer, L. J. (2005). Engineering ligand-receptor pairs for small molecule control of transcription. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/11651

Chicago Manual of Style (16th Edition):

Schwimmer, Lauren J. “Engineering ligand-receptor pairs for small molecule control of transcription.” 2005. Doctoral Dissertation, Georgia Tech. Accessed January 23, 2021. http://hdl.handle.net/1853/11651.

MLA Handbook (7th Edition):

Schwimmer, Lauren J. “Engineering ligand-receptor pairs for small molecule control of transcription.” 2005. Web. 23 Jan 2021.

Vancouver:

Schwimmer LJ. Engineering ligand-receptor pairs for small molecule control of transcription. [Internet] [Doctoral dissertation]. Georgia Tech; 2005. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/1853/11651.

Council of Science Editors:

Schwimmer LJ. Engineering ligand-receptor pairs for small molecule control of transcription. [Doctoral Dissertation]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/11651


Georgia Tech

9. Liu, Ying. Regulation of ceramide and its metabolites: biosynthesis and; in situ sphingolipid analysis.

Degree: PhD, Biology, 2010, Georgia Tech

 Sphingolipids are found in essentially all animals, plants and fungi, and some prokaryotic organisms and viruses. Sphingolipids function as structural components of membranes, lipoproteins, and… (more)

Subjects/Keywords: Tissue imaging mass spectrometry; Sulfatide; Ceramide; Electrospray tandem mass spectrometry; Glucosylceramide; Galactosylceramide; Sphingolipids; Ceramides; Liquid chromatography; Biosynthesis; Chromatographic analysis

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APA (6th Edition):

Liu, Y. (2010). Regulation of ceramide and its metabolites: biosynthesis and; in situ sphingolipid analysis. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/33918

Chicago Manual of Style (16th Edition):

Liu, Ying. “Regulation of ceramide and its metabolites: biosynthesis and; in situ sphingolipid analysis.” 2010. Doctoral Dissertation, Georgia Tech. Accessed January 23, 2021. http://hdl.handle.net/1853/33918.

MLA Handbook (7th Edition):

Liu, Ying. “Regulation of ceramide and its metabolites: biosynthesis and; in situ sphingolipid analysis.” 2010. Web. 23 Jan 2021.

Vancouver:

Liu Y. Regulation of ceramide and its metabolites: biosynthesis and; in situ sphingolipid analysis. [Internet] [Doctoral dissertation]. Georgia Tech; 2010. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/1853/33918.

Council of Science Editors:

Liu Y. Regulation of ceramide and its metabolites: biosynthesis and; in situ sphingolipid analysis. [Doctoral Dissertation]. Georgia Tech; 2010. Available from: http://hdl.handle.net/1853/33918


Georgia Tech

10. Urs, Nikhil Mahabir. The regulation of cellular trafficking of the human lysophosphatidic acid receptor 1: identification of the molecular determinants required for receptor trafficking.

Degree: PhD, Biology, 2007, Georgia Tech

 The following thesis research was undertaken to gain a better understanding of the mechanisms that regulate the cellular trafficking and signaling of the endothelial differentiation… (more)

Subjects/Keywords: Motifs; Cholesterol; PKC; LPA1; LPA; Beta-Arrestin; Trafficking; GPCR; Cell interaction; Lysophospholipids

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APA (6th Edition):

Urs, N. M. (2007). The regulation of cellular trafficking of the human lysophosphatidic acid receptor 1: identification of the molecular determinants required for receptor trafficking. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/16177

Chicago Manual of Style (16th Edition):

Urs, Nikhil Mahabir. “The regulation of cellular trafficking of the human lysophosphatidic acid receptor 1: identification of the molecular determinants required for receptor trafficking.” 2007. Doctoral Dissertation, Georgia Tech. Accessed January 23, 2021. http://hdl.handle.net/1853/16177.

MLA Handbook (7th Edition):

Urs, Nikhil Mahabir. “The regulation of cellular trafficking of the human lysophosphatidic acid receptor 1: identification of the molecular determinants required for receptor trafficking.” 2007. Web. 23 Jan 2021.

Vancouver:

Urs NM. The regulation of cellular trafficking of the human lysophosphatidic acid receptor 1: identification of the molecular determinants required for receptor trafficking. [Internet] [Doctoral dissertation]. Georgia Tech; 2007. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/1853/16177.

Council of Science Editors:

Urs NM. The regulation of cellular trafficking of the human lysophosphatidic acid receptor 1: identification of the molecular determinants required for receptor trafficking. [Doctoral Dissertation]. Georgia Tech; 2007. Available from: http://hdl.handle.net/1853/16177


Georgia Tech

11. Zhang, Xin. Development and Validation of a Nanodosimetry-Based Cell Survival Model for Mixed High- and Low-LET radiations.

Degree: PhD, Mechanical Engineering, 2006, Georgia Tech

 A new nanodosimetry-based cell survival model for mixed high- and low-LET radiations has been developed. The new model employs three dosimetry quantities and three biological… (more)

Subjects/Keywords: Cell survival model; V-79 cell survival curves; Fission neutron irradiation; Cells Effect of radiation on Mathematical models

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APA (6th Edition):

Zhang, X. (2006). Development and Validation of a Nanodosimetry-Based Cell Survival Model for Mixed High- and Low-LET radiations. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/11523

Chicago Manual of Style (16th Edition):

Zhang, Xin. “Development and Validation of a Nanodosimetry-Based Cell Survival Model for Mixed High- and Low-LET radiations.” 2006. Doctoral Dissertation, Georgia Tech. Accessed January 23, 2021. http://hdl.handle.net/1853/11523.

MLA Handbook (7th Edition):

Zhang, Xin. “Development and Validation of a Nanodosimetry-Based Cell Survival Model for Mixed High- and Low-LET radiations.” 2006. Web. 23 Jan 2021.

Vancouver:

Zhang X. Development and Validation of a Nanodosimetry-Based Cell Survival Model for Mixed High- and Low-LET radiations. [Internet] [Doctoral dissertation]. Georgia Tech; 2006. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/1853/11523.

Council of Science Editors:

Zhang X. Development and Validation of a Nanodosimetry-Based Cell Survival Model for Mixed High- and Low-LET radiations. [Doctoral Dissertation]. Georgia Tech; 2006. Available from: http://hdl.handle.net/1853/11523


Georgia Tech

12. Yang, Liuchun. Design, synthesis, and evaluation of fluorescent sensors for intracellular imaging of monovalent copper.

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

 The main theme of this thesis is to develop a fluorescent probe for imaging the subcellular distribution of kinetically labile copper pools that might play… (more)

Subjects/Keywords: Fluorescent sensor; Monovalent copper; Pyrazoline; PET; CTAP-1; Copper; Fluorescent probes; Chemical detectors

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APA (6th Edition):

Yang, L. (2005). Design, synthesis, and evaluation of fluorescent sensors for intracellular imaging of monovalent copper. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/11655

Chicago Manual of Style (16th Edition):

Yang, Liuchun. “Design, synthesis, and evaluation of fluorescent sensors for intracellular imaging of monovalent copper.” 2005. Doctoral Dissertation, Georgia Tech. Accessed January 23, 2021. http://hdl.handle.net/1853/11655.

MLA Handbook (7th Edition):

Yang, Liuchun. “Design, synthesis, and evaluation of fluorescent sensors for intracellular imaging of monovalent copper.” 2005. Web. 23 Jan 2021.

Vancouver:

Yang L. Design, synthesis, and evaluation of fluorescent sensors for intracellular imaging of monovalent copper. [Internet] [Doctoral dissertation]. Georgia Tech; 2005. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/1853/11655.

Council of Science Editors:

Yang L. Design, synthesis, and evaluation of fluorescent sensors for intracellular imaging of monovalent copper. [Doctoral Dissertation]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/11655


Georgia Tech

13. Salo, Paul David. Protein prenylation inhibitors reveal a novel role for rhoa and rhoc in trafficking of g protein-coupled receptors through recycling endosomes.

Degree: PhD, Chemistry and Biochemistry, 2007, Georgia Tech

 LPA1 lysophosphatidic acid receptors (LPA1Rs) are normally present on the surface of the cell. Our initial findings were that HMG-CoA reductase inhibitors (atorvastatin and mevastatin)… (more)

Subjects/Keywords: G protein-coupled receptors; Lysophosphatidic acid; Statin; GGTI; Statins (Cardiovascular agents); Sequestration (Chemistry); Endocytosis; Cell membranes

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APA (6th Edition):

Salo, P. D. (2007). Protein prenylation inhibitors reveal a novel role for rhoa and rhoc in trafficking of g protein-coupled receptors through recycling endosomes. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/26711

Chicago Manual of Style (16th Edition):

Salo, Paul David. “Protein prenylation inhibitors reveal a novel role for rhoa and rhoc in trafficking of g protein-coupled receptors through recycling endosomes.” 2007. Doctoral Dissertation, Georgia Tech. Accessed January 23, 2021. http://hdl.handle.net/1853/26711.

MLA Handbook (7th Edition):

Salo, Paul David. “Protein prenylation inhibitors reveal a novel role for rhoa and rhoc in trafficking of g protein-coupled receptors through recycling endosomes.” 2007. Web. 23 Jan 2021.

Vancouver:

Salo PD. Protein prenylation inhibitors reveal a novel role for rhoa and rhoc in trafficking of g protein-coupled receptors through recycling endosomes. [Internet] [Doctoral dissertation]. Georgia Tech; 2007. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/1853/26711.

Council of Science Editors:

Salo PD. Protein prenylation inhibitors reveal a novel role for rhoa and rhoc in trafficking of g protein-coupled receptors through recycling endosomes. [Doctoral Dissertation]. Georgia Tech; 2007. Available from: http://hdl.handle.net/1853/26711

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