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You searched for subject:(G protein coupled receptors). Showing records 1 – 30 of 27904 total matches.

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1. Mailhac, Camille. Développement d’outils pour l'étude de la signalisation médiée par les récepteurs couplés aux protéines G, basés sur l'utilisation d'anticorps à domaine unique de lama : Development of tools for the study of G protein-coupled receptor-mediated signaling based on the use of lama single domain antibodies.

Degree: Docteur es, Biologie. Immunologie, 2017, Aix Marseille Université

L'objectif principal de ma thèse était de développer de nouvelles technologies et des outils pour l’étude de l’activation des récepteurs couplés aux protéines G (GPCR).À… (more)

Subjects/Keywords: RCPG; G protein coupled receptors

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

APA (6th Edition):

Mailhac, C. (2017). Développement d’outils pour l'étude de la signalisation médiée par les récepteurs couplés aux protéines G, basés sur l'utilisation d'anticorps à domaine unique de lama : Development of tools for the study of G protein-coupled receptor-mediated signaling based on the use of lama single domain antibodies. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2017AIXM0405

Chicago Manual of Style (16th Edition):

Mailhac, Camille. “Développement d’outils pour l'étude de la signalisation médiée par les récepteurs couplés aux protéines G, basés sur l'utilisation d'anticorps à domaine unique de lama : Development of tools for the study of G protein-coupled receptor-mediated signaling based on the use of lama single domain antibodies.” 2017. Doctoral Dissertation, Aix Marseille Université. Accessed October 25, 2020. http://www.theses.fr/2017AIXM0405.

MLA Handbook (7th Edition):

Mailhac, Camille. “Développement d’outils pour l'étude de la signalisation médiée par les récepteurs couplés aux protéines G, basés sur l'utilisation d'anticorps à domaine unique de lama : Development of tools for the study of G protein-coupled receptor-mediated signaling based on the use of lama single domain antibodies.” 2017. Web. 25 Oct 2020.

Vancouver:

Mailhac C. Développement d’outils pour l'étude de la signalisation médiée par les récepteurs couplés aux protéines G, basés sur l'utilisation d'anticorps à domaine unique de lama : Development of tools for the study of G protein-coupled receptor-mediated signaling based on the use of lama single domain antibodies. [Internet] [Doctoral dissertation]. Aix Marseille Université 2017. [cited 2020 Oct 25]. Available from: http://www.theses.fr/2017AIXM0405.

Council of Science Editors:

Mailhac C. Développement d’outils pour l'étude de la signalisation médiée par les récepteurs couplés aux protéines G, basés sur l'utilisation d'anticorps à domaine unique de lama : Development of tools for the study of G protein-coupled receptor-mediated signaling based on the use of lama single domain antibodies. [Doctoral Dissertation]. Aix Marseille Université 2017. Available from: http://www.theses.fr/2017AIXM0405


University of Texas Southwestern Medical Center

2. Li, Tingting. Role of TGR5 in Bile Acid Metabolism.

Degree: 2011, University of Texas Southwestern Medical Center

 TGR5 is a G protein-coupled bile acid receptor present in various tissues in the body. Its agonism increases energy expenditure and lowers blood glucose. Thus,… (more)

Subjects/Keywords: Receptors, G-Protein-Coupled; Gallbladder; Metabolism

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APA (6th Edition):

Li, T. (2011). Role of TGR5 in Bile Acid Metabolism. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/869

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Li, Tingting. “Role of TGR5 in Bile Acid Metabolism.” 2011. Thesis, University of Texas Southwestern Medical Center. Accessed October 25, 2020. http://hdl.handle.net/2152.5/869.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Li, Tingting. “Role of TGR5 in Bile Acid Metabolism.” 2011. Web. 25 Oct 2020.

Vancouver:

Li T. Role of TGR5 in Bile Acid Metabolism. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2011. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/2152.5/869.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Li T. Role of TGR5 in Bile Acid Metabolism. [Thesis]. University of Texas Southwestern Medical Center; 2011. Available from: http://hdl.handle.net/2152.5/869

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of North Texas

3. Potbhare, Vrinda Nikhil. Expression of G-protein Coupled Receptors in Young and Mature Thrombocytes and Knockdown of Gpr18 in Zebrafish.

Degree: 2013, University of North Texas

 In this study, a novel method based on biotinylated antibodies and streptavidin coated magnetic beads was used to separate the thrombocyte subpopulations from zebrafish whole… (more)

Subjects/Keywords: Thrombocytes; G-protein coupled receptors; knockdown; zebrafish

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APA (6th Edition):

Potbhare, V. N. (2013). Expression of G-protein Coupled Receptors in Young and Mature Thrombocytes and Knockdown of Gpr18 in Zebrafish. (Thesis). University of North Texas. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc271881/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Potbhare, Vrinda Nikhil. “Expression of G-protein Coupled Receptors in Young and Mature Thrombocytes and Knockdown of Gpr18 in Zebrafish.” 2013. Thesis, University of North Texas. Accessed October 25, 2020. https://digital.library.unt.edu/ark:/67531/metadc271881/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Potbhare, Vrinda Nikhil. “Expression of G-protein Coupled Receptors in Young and Mature Thrombocytes and Knockdown of Gpr18 in Zebrafish.” 2013. Web. 25 Oct 2020.

Vancouver:

Potbhare VN. Expression of G-protein Coupled Receptors in Young and Mature Thrombocytes and Knockdown of Gpr18 in Zebrafish. [Internet] [Thesis]. University of North Texas; 2013. [cited 2020 Oct 25]. Available from: https://digital.library.unt.edu/ark:/67531/metadc271881/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Potbhare VN. Expression of G-protein Coupled Receptors in Young and Mature Thrombocytes and Knockdown of Gpr18 in Zebrafish. [Thesis]. University of North Texas; 2013. Available from: https://digital.library.unt.edu/ark:/67531/metadc271881/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Toronto

4. Sokolina, Ekaterina. Human GPCR Interactome and Investigation of the KCTD/beta2-adrenergic Receptor Interactions.

Degree: 2014, University of Toronto

G-protein-coupled receptors (GPCRs) are the largest family of transmembrane receptors with key roles in regulating signaling pathways targeted by therapeutics. To identify novel components of… (more)

Subjects/Keywords: cell signalling; G-protein coupled receptors; interactome; KCTDs; protein-protein interactions; receptors; 0487

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APA (6th Edition):

Sokolina, E. (2014). Human GPCR Interactome and Investigation of the KCTD/beta2-adrenergic Receptor Interactions. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/70192

Chicago Manual of Style (16th Edition):

Sokolina, Ekaterina. “Human GPCR Interactome and Investigation of the KCTD/beta2-adrenergic Receptor Interactions.” 2014. Masters Thesis, University of Toronto. Accessed October 25, 2020. http://hdl.handle.net/1807/70192.

MLA Handbook (7th Edition):

Sokolina, Ekaterina. “Human GPCR Interactome and Investigation of the KCTD/beta2-adrenergic Receptor Interactions.” 2014. Web. 25 Oct 2020.

Vancouver:

Sokolina E. Human GPCR Interactome and Investigation of the KCTD/beta2-adrenergic Receptor Interactions. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/1807/70192.

Council of Science Editors:

Sokolina E. Human GPCR Interactome and Investigation of the KCTD/beta2-adrenergic Receptor Interactions. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/70192


Vanderbilt University

5. Bender, Brian Joseph. Knowledge-Based Modeling of G-Protein Coupled Receptors and their Binding Partners.

Degree: PhD, Pharmacology, 2019, Vanderbilt University

G-protein coupled receptors (GPCRs) represent the largest family of membrane proteins and the most heavily targeted classes of proteins for therapeutic intervention. Relatively little is… (more)

Subjects/Keywords: protein modeling; rosetta; peptide docking; g-protein coupled receptors; ligand docking

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APA (6th Edition):

Bender, B. J. (2019). Knowledge-Based Modeling of G-Protein Coupled Receptors and their Binding Partners. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10445

Chicago Manual of Style (16th Edition):

Bender, Brian Joseph. “Knowledge-Based Modeling of G-Protein Coupled Receptors and their Binding Partners.” 2019. Doctoral Dissertation, Vanderbilt University. Accessed October 25, 2020. http://hdl.handle.net/1803/10445.

MLA Handbook (7th Edition):

Bender, Brian Joseph. “Knowledge-Based Modeling of G-Protein Coupled Receptors and their Binding Partners.” 2019. Web. 25 Oct 2020.

Vancouver:

Bender BJ. Knowledge-Based Modeling of G-Protein Coupled Receptors and their Binding Partners. [Internet] [Doctoral dissertation]. Vanderbilt University; 2019. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/1803/10445.

Council of Science Editors:

Bender BJ. Knowledge-Based Modeling of G-Protein Coupled Receptors and their Binding Partners. [Doctoral Dissertation]. Vanderbilt University; 2019. Available from: http://hdl.handle.net/1803/10445


Vanderbilt University

6. Wu, Yuantai. Functional study of g protein signaling during growth and development of the social amoeba Dictyostelium discoideum.

Degree: PhD, Biological Sciences, 2013, Vanderbilt University

 The social amoeba Dictyostelium discoideum senses the bacterial metabolite folic acid to track down bacteria. Previous studies suggested that the folic acid receptor is a… (more)

Subjects/Keywords: Galpha 8; Dictyostelium discoideum; G protein signaling; G protein-coupled receptors; GABA

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APA (6th Edition):

Wu, Y. (2013). Functional study of g protein signaling during growth and development of the social amoeba Dictyostelium discoideum. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13253

Chicago Manual of Style (16th Edition):

Wu, Yuantai. “Functional study of g protein signaling during growth and development of the social amoeba Dictyostelium discoideum.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed October 25, 2020. http://hdl.handle.net/1803/13253.

MLA Handbook (7th Edition):

Wu, Yuantai. “Functional study of g protein signaling during growth and development of the social amoeba Dictyostelium discoideum.” 2013. Web. 25 Oct 2020.

Vancouver:

Wu Y. Functional study of g protein signaling during growth and development of the social amoeba Dictyostelium discoideum. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/1803/13253.

Council of Science Editors:

Wu Y. Functional study of g protein signaling during growth and development of the social amoeba Dictyostelium discoideum. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://hdl.handle.net/1803/13253


University of Georgia

7. Altman, Molly Koertel. G-protein coupled receptor mediated signaling pathways in chemoresistant melanoma and ovarian cancer.

Degree: 2017, University of Georgia

 Cellular signaling pathways are involved in numerous physiological processes such as reproduction, growth, and the development of cancer and chemoresistance. G-protein coupled receptors (GPCRs) are… (more)

Subjects/Keywords: G-protein coupled receptors; Regulators of G-protein Signaling; chemoresistance; melanoma; ovarian cancer; angiogenesis

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APA (6th Edition):

Altman, M. K. (2017). G-protein coupled receptor mediated signaling pathways in chemoresistant melanoma and ovarian cancer. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/36560

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Altman, Molly Koertel. “G-protein coupled receptor mediated signaling pathways in chemoresistant melanoma and ovarian cancer.” 2017. Thesis, University of Georgia. Accessed October 25, 2020. http://hdl.handle.net/10724/36560.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Altman, Molly Koertel. “G-protein coupled receptor mediated signaling pathways in chemoresistant melanoma and ovarian cancer.” 2017. Web. 25 Oct 2020.

Vancouver:

Altman MK. G-protein coupled receptor mediated signaling pathways in chemoresistant melanoma and ovarian cancer. [Internet] [Thesis]. University of Georgia; 2017. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/10724/36560.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Altman MK. G-protein coupled receptor mediated signaling pathways in chemoresistant melanoma and ovarian cancer. [Thesis]. University of Georgia; 2017. Available from: http://hdl.handle.net/10724/36560

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Rochester

8. Leioatts, Nicholas. Allostery and Activation in the G Protein-Coupled Receptor, Rhodopsin.

Degree: PhD, 2014, University of Rochester

G protein-coupled receptors (GPCRs) are a biomedically important class of membrane proteins that are targeted by many small molecule drugs. These proteins act as molecular… (more)

Subjects/Keywords: G Protein-Coupled Receptors; Rhodopsin; Allostery; Signal Transduction

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APA (6th Edition):

Leioatts, N. (2014). Allostery and Activation in the G Protein-Coupled Receptor, Rhodopsin. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/28968

Chicago Manual of Style (16th Edition):

Leioatts, Nicholas. “Allostery and Activation in the G Protein-Coupled Receptor, Rhodopsin.” 2014. Doctoral Dissertation, University of Rochester. Accessed October 25, 2020. http://hdl.handle.net/1802/28968.

MLA Handbook (7th Edition):

Leioatts, Nicholas. “Allostery and Activation in the G Protein-Coupled Receptor, Rhodopsin.” 2014. Web. 25 Oct 2020.

Vancouver:

Leioatts N. Allostery and Activation in the G Protein-Coupled Receptor, Rhodopsin. [Internet] [Doctoral dissertation]. University of Rochester; 2014. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/1802/28968.

Council of Science Editors:

Leioatts N. Allostery and Activation in the G Protein-Coupled Receptor, Rhodopsin. [Doctoral Dissertation]. University of Rochester; 2014. Available from: http://hdl.handle.net/1802/28968


University of Saskatchewan

9. Kendall, Stephanie. Structural characterization of the N-terminal region of the Saccharomyces cerevisiae G-protein coupled receptor, Ste2p.

Degree: 2011, University of Saskatchewan

G-protein coupled receptors (GPCRs) form a superfamily of cell surface receptors with in excess of 2000 genes identified across taxa (Pierce et al., 2002). They… (more)

Subjects/Keywords: G-protein coupled receptors; Ste2p; Nuclear magnetic resonance; Circular Dichroism

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APA (6th Edition):

Kendall, S. (2011). Structural characterization of the N-terminal region of the Saccharomyces cerevisiae G-protein coupled receptor, Ste2p. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2011-07-114

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kendall, Stephanie. “Structural characterization of the N-terminal region of the Saccharomyces cerevisiae G-protein coupled receptor, Ste2p.” 2011. Thesis, University of Saskatchewan. Accessed October 25, 2020. http://hdl.handle.net/10388/ETD-2011-07-114.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kendall, Stephanie. “Structural characterization of the N-terminal region of the Saccharomyces cerevisiae G-protein coupled receptor, Ste2p.” 2011. Web. 25 Oct 2020.

Vancouver:

Kendall S. Structural characterization of the N-terminal region of the Saccharomyces cerevisiae G-protein coupled receptor, Ste2p. [Internet] [Thesis]. University of Saskatchewan; 2011. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/10388/ETD-2011-07-114.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kendall S. Structural characterization of the N-terminal region of the Saccharomyces cerevisiae G-protein coupled receptor, Ste2p. [Thesis]. University of Saskatchewan; 2011. Available from: http://hdl.handle.net/10388/ETD-2011-07-114

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Penn State University

10. Stahl, Edward L. MECHANISTIC STUDIES OF THE ALLOSTERIC MODULATION OF MUSCARINIC RECEPTORS .

Degree: 2012, Penn State University

 This dissertation is the result of a detailed investigation into the effects of the antiarrhythmic drug amiodarone on muscarinic receptors. We have found that amiodarone… (more)

Subjects/Keywords: G protein-coupled receptors; acetylcholine; muscarinic; allosteric; amiodarone

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APA (6th Edition):

Stahl, E. L. (2012). MECHANISTIC STUDIES OF THE ALLOSTERIC MODULATION OF MUSCARINIC RECEPTORS . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/12394

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Stahl, Edward L. “MECHANISTIC STUDIES OF THE ALLOSTERIC MODULATION OF MUSCARINIC RECEPTORS .” 2012. Thesis, Penn State University. Accessed October 25, 2020. https://submit-etda.libraries.psu.edu/catalog/12394.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Stahl, Edward L. “MECHANISTIC STUDIES OF THE ALLOSTERIC MODULATION OF MUSCARINIC RECEPTORS .” 2012. Web. 25 Oct 2020.

Vancouver:

Stahl EL. MECHANISTIC STUDIES OF THE ALLOSTERIC MODULATION OF MUSCARINIC RECEPTORS . [Internet] [Thesis]. Penn State University; 2012. [cited 2020 Oct 25]. Available from: https://submit-etda.libraries.psu.edu/catalog/12394.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Stahl EL. MECHANISTIC STUDIES OF THE ALLOSTERIC MODULATION OF MUSCARINIC RECEPTORS . [Thesis]. Penn State University; 2012. Available from: https://submit-etda.libraries.psu.edu/catalog/12394

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas Southwestern Medical Center

11. Fan, Chih-Wei 1982-. Chemically Based Interrogation of Smoothened, a Proto-Oncogenic Component of the Hedgehog Signal Transduction Pathway.

Degree: 2012, University of Texas Southwestern Medical Center

 Aberrant activation of the Hedgehog (Hh) signal transduction pathway is crucial for the initiation and maintenance of many cancer types. Underlying this deviant signaling process… (more)

Subjects/Keywords: Hedgehog Proteins; Receptors, G-Protein-Coupled; Signal Transduction

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APA (6th Edition):

Fan, C. 1. (2012). Chemically Based Interrogation of Smoothened, a Proto-Oncogenic Component of the Hedgehog Signal Transduction Pathway. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-58

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Fan, Chih-Wei 1982-. “Chemically Based Interrogation of Smoothened, a Proto-Oncogenic Component of the Hedgehog Signal Transduction Pathway.” 2012. Thesis, University of Texas Southwestern Medical Center. Accessed October 25, 2020. http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-58.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Fan, Chih-Wei 1982-. “Chemically Based Interrogation of Smoothened, a Proto-Oncogenic Component of the Hedgehog Signal Transduction Pathway.” 2012. Web. 25 Oct 2020.

Vancouver:

Fan C1. Chemically Based Interrogation of Smoothened, a Proto-Oncogenic Component of the Hedgehog Signal Transduction Pathway. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2012. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-58.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Fan C1. Chemically Based Interrogation of Smoothened, a Proto-Oncogenic Component of the Hedgehog Signal Transduction Pathway. [Thesis]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-58

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas Southwestern Medical Center

12. Ocal, Ozhan. Rgs16 is a Pancreatic Reporter of Chronic Hyperglycemia in Diabetes.

Degree: 2012, University of Texas Southwestern Medical Center

 Diabetes mellitus is a collection of metabolic diseases with chronic hyperglycemia as their common syndrome. Type 1 diabetes results from pancreatic insulin producing beta cell… (more)

Subjects/Keywords: Diabetes Mellitus, Type 1; RGS Proteins; Receptors, G-Protein-Coupled

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APA (6th Edition):

Ocal, O. (2012). Rgs16 is a Pancreatic Reporter of Chronic Hyperglycemia in Diabetes. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1034

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ocal, Ozhan. “Rgs16 is a Pancreatic Reporter of Chronic Hyperglycemia in Diabetes.” 2012. Thesis, University of Texas Southwestern Medical Center. Accessed October 25, 2020. http://hdl.handle.net/2152.5/1034.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ocal, Ozhan. “Rgs16 is a Pancreatic Reporter of Chronic Hyperglycemia in Diabetes.” 2012. Web. 25 Oct 2020.

Vancouver:

Ocal O. Rgs16 is a Pancreatic Reporter of Chronic Hyperglycemia in Diabetes. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2012. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/2152.5/1034.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ocal O. Rgs16 is a Pancreatic Reporter of Chronic Hyperglycemia in Diabetes. [Thesis]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/1034

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Illinois – Chicago

13. Hoeppner, Crystal Z. Identification of a Nuclear Localization Sequence in Beta-Arrestin1:Implications in NF- kB Activation.

Degree: 2012, University of Illinois – Chicago

 A mounting body of evidence suggests that beta-arrestin1 plays important roles in the nucleus, but how beta-arrestin1 enters the nucleus remains unclear since no nuclear… (more)

Subjects/Keywords: G Protein-Coupled Receptors; Transcription; Beta-Arrestin; Nuclear Localization

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APA (6th Edition):

Hoeppner, C. Z. (2012). Identification of a Nuclear Localization Sequence in Beta-Arrestin1:Implications in NF- kB Activation. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/9243

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Hoeppner, Crystal Z. “Identification of a Nuclear Localization Sequence in Beta-Arrestin1:Implications in NF- kB Activation.” 2012. Thesis, University of Illinois – Chicago. Accessed October 25, 2020. http://hdl.handle.net/10027/9243.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Hoeppner, Crystal Z. “Identification of a Nuclear Localization Sequence in Beta-Arrestin1:Implications in NF- kB Activation.” 2012. Web. 25 Oct 2020.

Vancouver:

Hoeppner CZ. Identification of a Nuclear Localization Sequence in Beta-Arrestin1:Implications in NF- kB Activation. [Internet] [Thesis]. University of Illinois – Chicago; 2012. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/10027/9243.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Hoeppner CZ. Identification of a Nuclear Localization Sequence in Beta-Arrestin1:Implications in NF- kB Activation. [Thesis]. University of Illinois – Chicago; 2012. Available from: http://hdl.handle.net/10027/9243

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Manchester

14. Omede, Ameh. Role of alpha-ketoglutarate receptor G-protein coupled receptor 99 (GPR99) in cardiac hypertrophy.

Degree: PhD, 2015, University of Manchester

 Cardiac hypertrophy and heart failure (HF) remains one of the major health problems in the UK and worldwide. However, advances in their management are limited… (more)

Subjects/Keywords: 616.1; Cardiac hypertrophy, heart failure, G-protein-coupled receptors

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APA (6th Edition):

Omede, A. (2015). Role of alpha-ketoglutarate receptor G-protein coupled receptor 99 (GPR99) in cardiac hypertrophy. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/role-of-alphaketoglutarate-receptor-gprotein-coupled-receptor-99-gpr99-in-cardiac-hypertrophy(83b04dba-5bfe-4623-ade1-12c779133b80).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.674688

Chicago Manual of Style (16th Edition):

Omede, Ameh. “Role of alpha-ketoglutarate receptor G-protein coupled receptor 99 (GPR99) in cardiac hypertrophy.” 2015. Doctoral Dissertation, University of Manchester. Accessed October 25, 2020. https://www.research.manchester.ac.uk/portal/en/theses/role-of-alphaketoglutarate-receptor-gprotein-coupled-receptor-99-gpr99-in-cardiac-hypertrophy(83b04dba-5bfe-4623-ade1-12c779133b80).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.674688.

MLA Handbook (7th Edition):

Omede, Ameh. “Role of alpha-ketoglutarate receptor G-protein coupled receptor 99 (GPR99) in cardiac hypertrophy.” 2015. Web. 25 Oct 2020.

Vancouver:

Omede A. Role of alpha-ketoglutarate receptor G-protein coupled receptor 99 (GPR99) in cardiac hypertrophy. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2020 Oct 25]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/role-of-alphaketoglutarate-receptor-gprotein-coupled-receptor-99-gpr99-in-cardiac-hypertrophy(83b04dba-5bfe-4623-ade1-12c779133b80).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.674688.

Council of Science Editors:

Omede A. Role of alpha-ketoglutarate receptor G-protein coupled receptor 99 (GPR99) in cardiac hypertrophy. [Doctoral Dissertation]. University of Manchester; 2015. Available from: https://www.research.manchester.ac.uk/portal/en/theses/role-of-alphaketoglutarate-receptor-gprotein-coupled-receptor-99-gpr99-in-cardiac-hypertrophy(83b04dba-5bfe-4623-ade1-12c779133b80).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.674688


Florida Atlantic University

15. Parker, Thomas A. A neuronal G protein-coupled receptor mediates the effect of diet on lifespan and development in Caenorhabditis elegans through autophagy.

Degree: 2019, Florida Atlantic University

Animals rely on the integration of a variety of external cues to understand and respond appropriately to their environment. The relative amounts of food and… (more)

Subjects/Keywords: Caenorhabditis elegans; Autophagy; Receptors, G-Protein-Coupled; Longevity; Diet

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APA (6th Edition):

Parker, T. A. (2019). A neuronal G protein-coupled receptor mediates the effect of diet on lifespan and development in Caenorhabditis elegans through autophagy. (Thesis). Florida Atlantic University. Retrieved from http://fau.digital.flvc.org/islandora/object/fau:41958

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Parker, Thomas A. “A neuronal G protein-coupled receptor mediates the effect of diet on lifespan and development in Caenorhabditis elegans through autophagy.” 2019. Thesis, Florida Atlantic University. Accessed October 25, 2020. http://fau.digital.flvc.org/islandora/object/fau:41958.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Parker, Thomas A. “A neuronal G protein-coupled receptor mediates the effect of diet on lifespan and development in Caenorhabditis elegans through autophagy.” 2019. Web. 25 Oct 2020.

Vancouver:

Parker TA. A neuronal G protein-coupled receptor mediates the effect of diet on lifespan and development in Caenorhabditis elegans through autophagy. [Internet] [Thesis]. Florida Atlantic University; 2019. [cited 2020 Oct 25]. Available from: http://fau.digital.flvc.org/islandora/object/fau:41958.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Parker TA. A neuronal G protein-coupled receptor mediates the effect of diet on lifespan and development in Caenorhabditis elegans through autophagy. [Thesis]. Florida Atlantic University; 2019. Available from: http://fau.digital.flvc.org/islandora/object/fau:41958

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Toronto

16. Redka, Dar'ya Sergiivna. Functional Properties of Monomers and Oligomers of the M2 Muscarinic Receptor.

Degree: PhD, 2014, University of Toronto

G protein-coupled receptors (GPCRs) are the largest family of membrane proteins and mediate signaling for a host of neurotransmitters, hormones and other stimuli from light… (more)

Subjects/Keywords: aggregation; cooperativity; G protein-coupled receptors; membrane reconstitution; monomers; oligomers; 0572

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APA (6th Edition):

Redka, D. S. (2014). Functional Properties of Monomers and Oligomers of the M2 Muscarinic Receptor. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/73777

Chicago Manual of Style (16th Edition):

Redka, Dar'ya Sergiivna. “Functional Properties of Monomers and Oligomers of the M2 Muscarinic Receptor.” 2014. Doctoral Dissertation, University of Toronto. Accessed October 25, 2020. http://hdl.handle.net/1807/73777.

MLA Handbook (7th Edition):

Redka, Dar'ya Sergiivna. “Functional Properties of Monomers and Oligomers of the M2 Muscarinic Receptor.” 2014. Web. 25 Oct 2020.

Vancouver:

Redka DS. Functional Properties of Monomers and Oligomers of the M2 Muscarinic Receptor. [Internet] [Doctoral dissertation]. University of Toronto; 2014. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/1807/73777.

Council of Science Editors:

Redka DS. Functional Properties of Monomers and Oligomers of the M2 Muscarinic Receptor. [Doctoral Dissertation]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/73777


University of Minnesota

17. Durkee, Caitlin. G Protein Signaling In Astrocytes Regulates Neuronal Excitability And Synaptic Plasticity.

Degree: PhD, Neuroscience, 2019, University of Minnesota

 Accumulating evidence over the past few decades has revealed that astrocytes, a type of glial cell in the brain, are more involved in active brain… (more)

Subjects/Keywords: astrocytes; calcium; cellular signaling; electrophysiology; gliotransmission; G protein-coupled receptors

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APA (6th Edition):

Durkee, C. (2019). G Protein Signaling In Astrocytes Regulates Neuronal Excitability And Synaptic Plasticity. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/203580

Chicago Manual of Style (16th Edition):

Durkee, Caitlin. “G Protein Signaling In Astrocytes Regulates Neuronal Excitability And Synaptic Plasticity.” 2019. Doctoral Dissertation, University of Minnesota. Accessed October 25, 2020. http://hdl.handle.net/11299/203580.

MLA Handbook (7th Edition):

Durkee, Caitlin. “G Protein Signaling In Astrocytes Regulates Neuronal Excitability And Synaptic Plasticity.” 2019. Web. 25 Oct 2020.

Vancouver:

Durkee C. G Protein Signaling In Astrocytes Regulates Neuronal Excitability And Synaptic Plasticity. [Internet] [Doctoral dissertation]. University of Minnesota; 2019. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/11299/203580.

Council of Science Editors:

Durkee C. G Protein Signaling In Astrocytes Regulates Neuronal Excitability And Synaptic Plasticity. [Doctoral Dissertation]. University of Minnesota; 2019. Available from: http://hdl.handle.net/11299/203580


Vanderbilt University

18. Fu, Darwin Yu. Improving Protein-Small Molecule Structure Predictions with Ensemble Methods, or Using Computers to Guess How Tiny Things Fit Together.

Degree: PhD, Chemistry, 2018, Vanderbilt University

Protein-small molecule structure prediction, or protein-ligand docking, is a computational method for modeling how binding partners will interaction on an atomic level. Accurate prediction of… (more)

Subjects/Keywords: Rosetta; Protein-Ligand Docking; Molecular Modeling; Small Molecules; G-Protein Coupled Receptors; Protein Structure Prediction

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APA (6th Edition):

Fu, D. Y. (2018). Improving Protein-Small Molecule Structure Predictions with Ensemble Methods, or Using Computers to Guess How Tiny Things Fit Together. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13786

Chicago Manual of Style (16th Edition):

Fu, Darwin Yu. “Improving Protein-Small Molecule Structure Predictions with Ensemble Methods, or Using Computers to Guess How Tiny Things Fit Together.” 2018. Doctoral Dissertation, Vanderbilt University. Accessed October 25, 2020. http://hdl.handle.net/1803/13786.

MLA Handbook (7th Edition):

Fu, Darwin Yu. “Improving Protein-Small Molecule Structure Predictions with Ensemble Methods, or Using Computers to Guess How Tiny Things Fit Together.” 2018. Web. 25 Oct 2020.

Vancouver:

Fu DY. Improving Protein-Small Molecule Structure Predictions with Ensemble Methods, or Using Computers to Guess How Tiny Things Fit Together. [Internet] [Doctoral dissertation]. Vanderbilt University; 2018. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/1803/13786.

Council of Science Editors:

Fu DY. Improving Protein-Small Molecule Structure Predictions with Ensemble Methods, or Using Computers to Guess How Tiny Things Fit Together. [Doctoral Dissertation]. Vanderbilt University; 2018. Available from: http://hdl.handle.net/1803/13786


University of Texas Southwestern Medical Center

19. Liao, Yuxing. Evolutionary Classification of Protein Domains: From Remote Homology to Family.

Degree: 2017, University of Texas Southwestern Medical Center

 Understanding the evolution of a protein, including both close and distant relationships, often reveals insight into its structure and function. A protein domain classification splits… (more)

Subjects/Keywords: Computational Biology; Databases, Protein; Protein Structure, Tertiary; Proteins; Receptors, G-Protein-Coupled; Terminology as Topic

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APA (6th Edition):

Liao, Y. (2017). Evolutionary Classification of Protein Domains: From Remote Homology to Family. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/7740

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Liao, Yuxing. “Evolutionary Classification of Protein Domains: From Remote Homology to Family.” 2017. Thesis, University of Texas Southwestern Medical Center. Accessed October 25, 2020. http://hdl.handle.net/2152.5/7740.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Liao, Yuxing. “Evolutionary Classification of Protein Domains: From Remote Homology to Family.” 2017. Web. 25 Oct 2020.

Vancouver:

Liao Y. Evolutionary Classification of Protein Domains: From Remote Homology to Family. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2017. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/2152.5/7740.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Liao Y. Evolutionary Classification of Protein Domains: From Remote Homology to Family. [Thesis]. University of Texas Southwestern Medical Center; 2017. Available from: http://hdl.handle.net/2152.5/7740

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Western Ontario

20. Tutunea-Fatan, Elena. Signal Transduction Mechanisms Mediating the Regulation of Vascular G Protein-Coupled Receptors.

Degree: 2016, University of Western Ontario

 Blood pressure homeostasis is controlled via a complex network of cell signaling mechanisms. Among the broad network of receptors and signaling molecules regulating blood vessel… (more)

Subjects/Keywords: G protein-coupled receptors; G protein-coupled receptor kinases; Rab4GTPase; signal transduction; vascular smooth muscle cells; hypertension; Cardiovascular Diseases

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APA (6th Edition):

Tutunea-Fatan, E. (2016). Signal Transduction Mechanisms Mediating the Regulation of Vascular G Protein-Coupled Receptors. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/4329

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Tutunea-Fatan, Elena. “Signal Transduction Mechanisms Mediating the Regulation of Vascular G Protein-Coupled Receptors.” 2016. Thesis, University of Western Ontario. Accessed October 25, 2020. https://ir.lib.uwo.ca/etd/4329.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Tutunea-Fatan, Elena. “Signal Transduction Mechanisms Mediating the Regulation of Vascular G Protein-Coupled Receptors.” 2016. Web. 25 Oct 2020.

Vancouver:

Tutunea-Fatan E. Signal Transduction Mechanisms Mediating the Regulation of Vascular G Protein-Coupled Receptors. [Internet] [Thesis]. University of Western Ontario; 2016. [cited 2020 Oct 25]. Available from: https://ir.lib.uwo.ca/etd/4329.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Tutunea-Fatan E. Signal Transduction Mechanisms Mediating the Regulation of Vascular G Protein-Coupled Receptors. [Thesis]. University of Western Ontario; 2016. Available from: https://ir.lib.uwo.ca/etd/4329

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universitat Pompeu Fabra

21. Sallander, Eva Jessica. The mechanism of G protein coupled receptor activation: the serotonin receptors.

Degree: Departament de Ciències Experimentals i de la Salut, 2011, Universitat Pompeu Fabra

 One of the main questions in G protein coupled receptors (GPCRs) molecular pharmacology is to understand the structural arrangements of the seven transmembrane (TM) helices… (more)

Subjects/Keywords: GPCRs; G protein coupled receptors; Serotonin; Transmembrane; 5-HT6; 5-HT4; 5-HT7; Receptors de la serotonina; Proteïnes G  – receptors; 577

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APA (6th Edition):

Sallander, E. J. (2011). The mechanism of G protein coupled receptor activation: the serotonin receptors. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/77901

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Sallander, Eva Jessica. “The mechanism of G protein coupled receptor activation: the serotonin receptors.” 2011. Thesis, Universitat Pompeu Fabra. Accessed October 25, 2020. http://hdl.handle.net/10803/77901.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Sallander, Eva Jessica. “The mechanism of G protein coupled receptor activation: the serotonin receptors.” 2011. Web. 25 Oct 2020.

Vancouver:

Sallander EJ. The mechanism of G protein coupled receptor activation: the serotonin receptors. [Internet] [Thesis]. Universitat Pompeu Fabra; 2011. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/10803/77901.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Sallander EJ. The mechanism of G protein coupled receptor activation: the serotonin receptors. [Thesis]. Universitat Pompeu Fabra; 2011. Available from: http://hdl.handle.net/10803/77901

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

22. Theodoropoulou, Margarita. Υπολογιστικές μελέτες σε συζευγμένους με G-πρωτεΐνες υποδοχείς (GPCRS).

Degree: 2014, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

In the context of this thesis, using computational methods, we studied extensively, the very interesting superfamily of GPCRs and their partners, G-proteins. Two methods were… (more)

Subjects/Keywords: Μεταγωγή σήματος; Βιοπληροφορική; Συζευγμένοι με g-πρωτεΐνες υποδοχείς; Signal transduction; Bioinformatics; G-protein coupled receptors

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APA (6th Edition):

Theodoropoulou, M. (2014). Υπολογιστικές μελέτες σε συζευγμένους με G-πρωτεΐνες υποδοχείς (GPCRS). (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/44283

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Theodoropoulou, Margarita. “Υπολογιστικές μελέτες σε συζευγμένους με G-πρωτεΐνες υποδοχείς (GPCRS).” 2014. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed October 25, 2020. http://hdl.handle.net/10442/hedi/44283.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Theodoropoulou, Margarita. “Υπολογιστικές μελέτες σε συζευγμένους με G-πρωτεΐνες υποδοχείς (GPCRS).” 2014. Web. 25 Oct 2020.

Vancouver:

Theodoropoulou M. Υπολογιστικές μελέτες σε συζευγμένους με G-πρωτεΐνες υποδοχείς (GPCRS). [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/10442/hedi/44283.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Theodoropoulou M. Υπολογιστικές μελέτες σε συζευγμένους με G-πρωτεΐνες υποδοχείς (GPCRS). [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. Available from: http://hdl.handle.net/10442/hedi/44283

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

23. Stephens, Bryan Scott. Understanding CXC chemokine receptor 4 activation by CXC chemokine ligand 12.

Degree: Biomedical Sciences, 2017, University of California – San Diego

 The past several years have seen a rapid advancement in our understanding of how CXCR4 transmits the extracellular CXCL12 signal into intracellular signaling, which ultimately… (more)

Subjects/Keywords: Pharmacology; Pharmaceutical sciences; Cellular biology; Chemokine receptors; Chemokines; G protein-coupled receptors

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APA (6th Edition):

Stephens, B. S. (2017). Understanding CXC chemokine receptor 4 activation by CXC chemokine ligand 12. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/3zt5h403

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Stephens, Bryan Scott. “Understanding CXC chemokine receptor 4 activation by CXC chemokine ligand 12.” 2017. Thesis, University of California – San Diego. Accessed October 25, 2020. http://www.escholarship.org/uc/item/3zt5h403.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Stephens, Bryan Scott. “Understanding CXC chemokine receptor 4 activation by CXC chemokine ligand 12.” 2017. Web. 25 Oct 2020.

Vancouver:

Stephens BS. Understanding CXC chemokine receptor 4 activation by CXC chemokine ligand 12. [Internet] [Thesis]. University of California – San Diego; 2017. [cited 2020 Oct 25]. Available from: http://www.escholarship.org/uc/item/3zt5h403.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Stephens BS. Understanding CXC chemokine receptor 4 activation by CXC chemokine ligand 12. [Thesis]. University of California – San Diego; 2017. Available from: http://www.escholarship.org/uc/item/3zt5h403

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Toronto

24. Shivnaraine, Rabindra Vishwadev. On the Nature of Allosteric Interactions at the M2 Muscarinic Receptor.

Degree: PhD, 2015, University of Toronto

G protein-coupled receptors (GPCRs) are allosteric machines that constitute the largest family of membrane bound receptors. Members of the family 1a GPCRs such as the… (more)

Subjects/Keywords: allosteric modulators; cooperativity; G protein coupled receptors; mechansitic modelling; molecular dynamics; Muscarinic receptors; 0572

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APA (6th Edition):

Shivnaraine, R. V. (2015). On the Nature of Allosteric Interactions at the M2 Muscarinic Receptor. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/69491

Chicago Manual of Style (16th Edition):

Shivnaraine, Rabindra Vishwadev. “On the Nature of Allosteric Interactions at the M2 Muscarinic Receptor.” 2015. Doctoral Dissertation, University of Toronto. Accessed October 25, 2020. http://hdl.handle.net/1807/69491.

MLA Handbook (7th Edition):

Shivnaraine, Rabindra Vishwadev. “On the Nature of Allosteric Interactions at the M2 Muscarinic Receptor.” 2015. Web. 25 Oct 2020.

Vancouver:

Shivnaraine RV. On the Nature of Allosteric Interactions at the M2 Muscarinic Receptor. [Internet] [Doctoral dissertation]. University of Toronto; 2015. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/1807/69491.

Council of Science Editors:

Shivnaraine RV. On the Nature of Allosteric Interactions at the M2 Muscarinic Receptor. [Doctoral Dissertation]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/69491


University of Guelph

25. Patel, Ashutosh. Muscarinic Receptor Isoforms Differentially Regulate the Excitability of Medial Prefrontal Cortex Layer 6 Pyramidal Neurons in CD-1 mice.

Degree: MS, Department of Biomedical Sciences, 2018, University of Guelph

 Cholinergic signalling within the medial prefrontal cortex (mPFC) plays an important modulatory role in mPFC-dependent cognitive functions. This role is mediated by acetylcholine (ACh) activation… (more)

Subjects/Keywords: Muscarinic Receptors; Cholinergic Signalling; Acetylcholine; Electrophysiology; G Protein Coupled Receptors; Medial Prefrontal Cortex

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APA (6th Edition):

Patel, A. (2018). Muscarinic Receptor Isoforms Differentially Regulate the Excitability of Medial Prefrontal Cortex Layer 6 Pyramidal Neurons in CD-1 mice. (Masters Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/14161

Chicago Manual of Style (16th Edition):

Patel, Ashutosh. “Muscarinic Receptor Isoforms Differentially Regulate the Excitability of Medial Prefrontal Cortex Layer 6 Pyramidal Neurons in CD-1 mice.” 2018. Masters Thesis, University of Guelph. Accessed October 25, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/14161.

MLA Handbook (7th Edition):

Patel, Ashutosh. “Muscarinic Receptor Isoforms Differentially Regulate the Excitability of Medial Prefrontal Cortex Layer 6 Pyramidal Neurons in CD-1 mice.” 2018. Web. 25 Oct 2020.

Vancouver:

Patel A. Muscarinic Receptor Isoforms Differentially Regulate the Excitability of Medial Prefrontal Cortex Layer 6 Pyramidal Neurons in CD-1 mice. [Internet] [Masters thesis]. University of Guelph; 2018. [cited 2020 Oct 25]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/14161.

Council of Science Editors:

Patel A. Muscarinic Receptor Isoforms Differentially Regulate the Excitability of Medial Prefrontal Cortex Layer 6 Pyramidal Neurons in CD-1 mice. [Masters Thesis]. University of Guelph; 2018. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/14161


East Carolina University

26. Krewson, Elizabeth. THE PRO-INFLAMMATORY ROLE OF G-PROTEIN COUPLED RECEPTOR 4 IN AN ACIDIC MICROENVIRONMENT.

Degree: PhD, PHD-Anatomy and Cell Biology, 2018, East Carolina University

 The endothelium of the microvascular system serves an ideal mediator between circulating blood and tissues in order to regulate systemic homeostasis. During vascular disease, the… (more)

Subjects/Keywords: Acidic; Ischemia; disease; cytoskeletal; endothelial cells; signaling; Receptors, G-Protein-Coupled; GPR4 protein, human

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APA (6th Edition):

Krewson, E. (2018). THE PRO-INFLAMMATORY ROLE OF G-PROTEIN COUPLED RECEPTOR 4 IN AN ACIDIC MICROENVIRONMENT. (Doctoral Dissertation). East Carolina University. Retrieved from http://hdl.handle.net/10342/6975

Chicago Manual of Style (16th Edition):

Krewson, Elizabeth. “THE PRO-INFLAMMATORY ROLE OF G-PROTEIN COUPLED RECEPTOR 4 IN AN ACIDIC MICROENVIRONMENT.” 2018. Doctoral Dissertation, East Carolina University. Accessed October 25, 2020. http://hdl.handle.net/10342/6975.

MLA Handbook (7th Edition):

Krewson, Elizabeth. “THE PRO-INFLAMMATORY ROLE OF G-PROTEIN COUPLED RECEPTOR 4 IN AN ACIDIC MICROENVIRONMENT.” 2018. Web. 25 Oct 2020.

Vancouver:

Krewson E. THE PRO-INFLAMMATORY ROLE OF G-PROTEIN COUPLED RECEPTOR 4 IN AN ACIDIC MICROENVIRONMENT. [Internet] [Doctoral dissertation]. East Carolina University; 2018. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/10342/6975.

Council of Science Editors:

Krewson E. THE PRO-INFLAMMATORY ROLE OF G-PROTEIN COUPLED RECEPTOR 4 IN AN ACIDIC MICROENVIRONMENT. [Doctoral Dissertation]. East Carolina University; 2018. Available from: http://hdl.handle.net/10342/6975


New Jersey Institute of Technology

27. Kim, Alyssa Misoo. Engineering spores to display g protein-coupled receptors for directed evolution.

Degree: MSin Pharmaceutical Engineering - (M.S.), Chemical, Biological and Pharmaceutical Engineering, 2013, New Jersey Institute of Technology

  All human cells are surrounded by a plasma membrane made from a phospholipid bilayer, which is responsible for maintaining a biologically active species, while… (more)

Subjects/Keywords: Protein engineering; G protein-coupled receptors; Chemical Engineering; Pharmaceutics and Drug Design

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

APA (6th Edition):

Kim, A. M. (2013). Engineering spores to display g protein-coupled receptors for directed evolution. (Thesis). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/theses/174

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kim, Alyssa Misoo. “Engineering spores to display g protein-coupled receptors for directed evolution.” 2013. Thesis, New Jersey Institute of Technology. Accessed October 25, 2020. https://digitalcommons.njit.edu/theses/174.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kim, Alyssa Misoo. “Engineering spores to display g protein-coupled receptors for directed evolution.” 2013. Web. 25 Oct 2020.

Vancouver:

Kim AM. Engineering spores to display g protein-coupled receptors for directed evolution. [Internet] [Thesis]. New Jersey Institute of Technology; 2013. [cited 2020 Oct 25]. Available from: https://digitalcommons.njit.edu/theses/174.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kim AM. Engineering spores to display g protein-coupled receptors for directed evolution. [Thesis]. New Jersey Institute of Technology; 2013. Available from: https://digitalcommons.njit.edu/theses/174

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Iowa

28. Stewart, Adele Marie. Regulator of G protein signaling 6 (RGS6), a multifarious and pleiotropic modulator of G protein coupled receptor signaling in brain.

Degree: PhD, Pharmacology, 2014, University of Iowa

  Transmembrane signal transduction by ligand-activated G protein-coupled receptors (GPCRs) controls virtually every aspect of mammalian physiology, and this receptor class is the target of… (more)

Subjects/Keywords: alternative splicing; G protein coupled receptors; knockout mouse; neuropsychiatric disorders; protein phosphorylation; Regulators of G protein signaling; Pharmacology

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

APA (6th Edition):

Stewart, A. M. (2014). Regulator of G protein signaling 6 (RGS6), a multifarious and pleiotropic modulator of G protein coupled receptor signaling in brain. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/4765

Chicago Manual of Style (16th Edition):

Stewart, Adele Marie. “Regulator of G protein signaling 6 (RGS6), a multifarious and pleiotropic modulator of G protein coupled receptor signaling in brain.” 2014. Doctoral Dissertation, University of Iowa. Accessed October 25, 2020. https://ir.uiowa.edu/etd/4765.

MLA Handbook (7th Edition):

Stewart, Adele Marie. “Regulator of G protein signaling 6 (RGS6), a multifarious and pleiotropic modulator of G protein coupled receptor signaling in brain.” 2014. Web. 25 Oct 2020.

Vancouver:

Stewart AM. Regulator of G protein signaling 6 (RGS6), a multifarious and pleiotropic modulator of G protein coupled receptor signaling in brain. [Internet] [Doctoral dissertation]. University of Iowa; 2014. [cited 2020 Oct 25]. Available from: https://ir.uiowa.edu/etd/4765.

Council of Science Editors:

Stewart AM. Regulator of G protein signaling 6 (RGS6), a multifarious and pleiotropic modulator of G protein coupled receptor signaling in brain. [Doctoral Dissertation]. University of Iowa; 2014. Available from: https://ir.uiowa.edu/etd/4765


Dalhousie University

29. Hammad, Maha. CHARACTERIZATION OF THE ANGIOTENSIN TYPE 1 RECEPTOR AND THE BETA2 ADRENERGIC RECEPTOR PROPERTIES: THE INVOLVEMENT OF ARRESTIN2, RAB1 AND SOME MOLECULAR CHAPERONES IN THE ASSEMBLY AND TRAFFICKING OF GPCRS.

Degree: MS, Department of Pharmacology, 2010, Dalhousie University

 Current drugs used to treat Congestive Heart Failure target the renin-angiotensin and adrenergic systems. Studies showed increased mortality rates in patients treated with a combination… (more)

Subjects/Keywords: G Protein Coupled Receptors; Congestive Heart Failure; Adrenergic Receptors; Angiotensin Receptors; Rab GTPases; Molecular Chaperones; Bimolecular Fluorescence Complementation; GPCRs Oligomerization

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

APA (6th Edition):

Hammad, M. (2010). CHARACTERIZATION OF THE ANGIOTENSIN TYPE 1 RECEPTOR AND THE BETA2 ADRENERGIC RECEPTOR PROPERTIES: THE INVOLVEMENT OF ARRESTIN2, RAB1 AND SOME MOLECULAR CHAPERONES IN THE ASSEMBLY AND TRAFFICKING OF GPCRS. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/13068

Chicago Manual of Style (16th Edition):

Hammad, Maha. “CHARACTERIZATION OF THE ANGIOTENSIN TYPE 1 RECEPTOR AND THE BETA2 ADRENERGIC RECEPTOR PROPERTIES: THE INVOLVEMENT OF ARRESTIN2, RAB1 AND SOME MOLECULAR CHAPERONES IN THE ASSEMBLY AND TRAFFICKING OF GPCRS.” 2010. Masters Thesis, Dalhousie University. Accessed October 25, 2020. http://hdl.handle.net/10222/13068.

MLA Handbook (7th Edition):

Hammad, Maha. “CHARACTERIZATION OF THE ANGIOTENSIN TYPE 1 RECEPTOR AND THE BETA2 ADRENERGIC RECEPTOR PROPERTIES: THE INVOLVEMENT OF ARRESTIN2, RAB1 AND SOME MOLECULAR CHAPERONES IN THE ASSEMBLY AND TRAFFICKING OF GPCRS.” 2010. Web. 25 Oct 2020.

Vancouver:

Hammad M. CHARACTERIZATION OF THE ANGIOTENSIN TYPE 1 RECEPTOR AND THE BETA2 ADRENERGIC RECEPTOR PROPERTIES: THE INVOLVEMENT OF ARRESTIN2, RAB1 AND SOME MOLECULAR CHAPERONES IN THE ASSEMBLY AND TRAFFICKING OF GPCRS. [Internet] [Masters thesis]. Dalhousie University; 2010. [cited 2020 Oct 25]. Available from: http://hdl.handle.net/10222/13068.

Council of Science Editors:

Hammad M. CHARACTERIZATION OF THE ANGIOTENSIN TYPE 1 RECEPTOR AND THE BETA2 ADRENERGIC RECEPTOR PROPERTIES: THE INVOLVEMENT OF ARRESTIN2, RAB1 AND SOME MOLECULAR CHAPERONES IN THE ASSEMBLY AND TRAFFICKING OF GPCRS. [Masters Thesis]. Dalhousie University; 2010. Available from: http://hdl.handle.net/10222/13068

30. Lee, Katherine N. Regulation of Cardiac Hypertrophy and Metabolism by Regulator of G Protein Signalling 2 (RGS2).

Degree: 2017, University of Western Ontario

 Pathological left ventricular hypertrophy is a maladaptive cardiomyocyte growth response to various cardiovascular conditions such as hypertension, and is a major risk factor for heart… (more)

Subjects/Keywords: Regulator of G protein signalling 2 (RGS2); eIF2 and eIF2B; G protein-coupled receptors (GPCRs); cardiac hypertrophy; metabolism; lean phenotype

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

APA (6th Edition):

Lee, K. N. (2017). Regulation of Cardiac Hypertrophy and Metabolism by Regulator of G Protein Signalling 2 (RGS2). (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/4929

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Lee, Katherine N. “Regulation of Cardiac Hypertrophy and Metabolism by Regulator of G Protein Signalling 2 (RGS2).” 2017. Thesis, University of Western Ontario. Accessed October 25, 2020. https://ir.lib.uwo.ca/etd/4929.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Lee, Katherine N. “Regulation of Cardiac Hypertrophy and Metabolism by Regulator of G Protein Signalling 2 (RGS2).” 2017. Web. 25 Oct 2020.

Vancouver:

Lee KN. Regulation of Cardiac Hypertrophy and Metabolism by Regulator of G Protein Signalling 2 (RGS2). [Internet] [Thesis]. University of Western Ontario; 2017. [cited 2020 Oct 25]. Available from: https://ir.lib.uwo.ca/etd/4929.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Lee KN. Regulation of Cardiac Hypertrophy and Metabolism by Regulator of G Protein Signalling 2 (RGS2). [Thesis]. University of Western Ontario; 2017. Available from: https://ir.lib.uwo.ca/etd/4929

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

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