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Dates: 2015 – 2019

You searched for subject:(functional selectivity). Showing records 1 – 16 of 16 total matches.

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University of Kansas

1. Johnson, Stephanie. Design and Synthesis of Functionally Selective Kappa Opioid Receptor Ligands.

Degree: MS, Medicinal Chemistry, 2017, University of Kansas

 The ability of ligands to differentially regulate the activity of signaling pathways coupled to a receptor potentially enables researchers to optimize therapeutically relevant efficacies, while… (more)

Subjects/Keywords: Pharmaceutical sciences; Organic chemistry; Chemistry; functional; kappa; opioid; selectivity; U50; 488

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

APA (6th Edition):

Johnson, S. (2017). Design and Synthesis of Functionally Selective Kappa Opioid Receptor Ligands. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/26154

Chicago Manual of Style (16th Edition):

Johnson, Stephanie. “Design and Synthesis of Functionally Selective Kappa Opioid Receptor Ligands.” 2017. Masters Thesis, University of Kansas. Accessed December 09, 2019. http://hdl.handle.net/1808/26154.

MLA Handbook (7th Edition):

Johnson, Stephanie. “Design and Synthesis of Functionally Selective Kappa Opioid Receptor Ligands.” 2017. Web. 09 Dec 2019.

Vancouver:

Johnson S. Design and Synthesis of Functionally Selective Kappa Opioid Receptor Ligands. [Internet] [Masters thesis]. University of Kansas; 2017. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/1808/26154.

Council of Science Editors:

Johnson S. Design and Synthesis of Functionally Selective Kappa Opioid Receptor Ligands. [Masters Thesis]. University of Kansas; 2017. Available from: http://hdl.handle.net/1808/26154


Purdue University

2. Brust Fernandes, Tarsis. FUNCTIONAL SELECTIVITY DOWNSTREAM OF Gαi/o-COUPLED RECEPTORS.

Degree: PhD, Medicinal Chemistry and Molecular Pharmacology, 2015, Purdue University

 G protein-coupled receptors (GPCRs) are drug targets that often activate multiple signaling pathways. The multiple GPCR responses provide opportunities for biased or functionally selective ligands… (more)

Subjects/Keywords: adenylyl cyclase; beta-arrestin; biased signaling; functional selectivity; GPCR; G protein

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APA (6th Edition):

Brust Fernandes, T. (2015). FUNCTIONAL SELECTIVITY DOWNSTREAM OF Gαi/o-COUPLED RECEPTORS. (Doctoral Dissertation). Purdue University. Retrieved from https://docs.lib.purdue.edu/open_access_dissertations/1448

Chicago Manual of Style (16th Edition):

Brust Fernandes, Tarsis. “FUNCTIONAL SELECTIVITY DOWNSTREAM OF Gαi/o-COUPLED RECEPTORS.” 2015. Doctoral Dissertation, Purdue University. Accessed December 09, 2019. https://docs.lib.purdue.edu/open_access_dissertations/1448.

MLA Handbook (7th Edition):

Brust Fernandes, Tarsis. “FUNCTIONAL SELECTIVITY DOWNSTREAM OF Gαi/o-COUPLED RECEPTORS.” 2015. Web. 09 Dec 2019.

Vancouver:

Brust Fernandes T. FUNCTIONAL SELECTIVITY DOWNSTREAM OF Gαi/o-COUPLED RECEPTORS. [Internet] [Doctoral dissertation]. Purdue University; 2015. [cited 2019 Dec 09]. Available from: https://docs.lib.purdue.edu/open_access_dissertations/1448.

Council of Science Editors:

Brust Fernandes T. FUNCTIONAL SELECTIVITY DOWNSTREAM OF Gαi/o-COUPLED RECEPTORS. [Doctoral Dissertation]. Purdue University; 2015. Available from: https://docs.lib.purdue.edu/open_access_dissertations/1448


UCLA

3. Yu, Peiyuan. Computational Studies on the Reactivity, Selectivity and Molecular Dynamics of Cycloaddition Reactions.

Degree: Chemistry, 2017, UCLA

 The first part of this dissertation describes computational studies of higher-order cycloadditions with a focus on elucidating the origins of periselectivity. These reactions involve ambimodal… (more)

Subjects/Keywords: Chemistry; Organic chemistry; Cycloaddition; Density Functional Theory; Diels–Alder; Molecular Dynamics; Reactivity; Selectivity

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APA (6th Edition):

Yu, P. (2017). Computational Studies on the Reactivity, Selectivity and Molecular Dynamics of Cycloaddition Reactions. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/1jk894mq

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):

Yu, Peiyuan. “Computational Studies on the Reactivity, Selectivity and Molecular Dynamics of Cycloaddition Reactions.” 2017. Thesis, UCLA. Accessed December 09, 2019. http://www.escholarship.org/uc/item/1jk894mq.

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

MLA Handbook (7th Edition):

Yu, Peiyuan. “Computational Studies on the Reactivity, Selectivity and Molecular Dynamics of Cycloaddition Reactions.” 2017. Web. 09 Dec 2019.

Vancouver:

Yu P. Computational Studies on the Reactivity, Selectivity and Molecular Dynamics of Cycloaddition Reactions. [Internet] [Thesis]. UCLA; 2017. [cited 2019 Dec 09]. Available from: http://www.escholarship.org/uc/item/1jk894mq.

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

Council of Science Editors:

Yu P. Computational Studies on the Reactivity, Selectivity and Molecular Dynamics of Cycloaddition Reactions. [Thesis]. UCLA; 2017. Available from: http://www.escholarship.org/uc/item/1jk894mq

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


Freie Universität Berlin

4. Dinter, Juliane. Functional selectivity of G-Protein coupled receptors with a role in energy homeostasis.

Degree: 2015, Freie Universität Berlin

 G-protein coupled receptors (GPCRs) are involved in the control of all basic cellular and physiological functions such as metabolism, cell differentiation and growth. The characteristics… (more)

Subjects/Keywords: GPCR; functional selectivity; energy homeostasis; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Dinter, J. (2015). Functional selectivity of G-Protein coupled receptors with a role in energy homeostasis. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-10264

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):

Dinter, Juliane. “Functional selectivity of G-Protein coupled receptors with a role in energy homeostasis.” 2015. Thesis, Freie Universität Berlin. Accessed December 09, 2019. http://dx.doi.org/10.17169/refubium-10264.

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

MLA Handbook (7th Edition):

Dinter, Juliane. “Functional selectivity of G-Protein coupled receptors with a role in energy homeostasis.” 2015. Web. 09 Dec 2019.

Vancouver:

Dinter J. Functional selectivity of G-Protein coupled receptors with a role in energy homeostasis. [Internet] [Thesis]. Freie Universität Berlin; 2015. [cited 2019 Dec 09]. Available from: http://dx.doi.org/10.17169/refubium-10264.

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

Council of Science Editors:

Dinter J. Functional selectivity of G-Protein coupled receptors with a role in energy homeostasis. [Thesis]. Freie Universität Berlin; 2015. Available from: http://dx.doi.org/10.17169/refubium-10264

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


University of Arizona

5. Olson, Keith Mathew. Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling .

Degree: 2017, University of Arizona

 Most clinical opioids produce analgesia through the Mu Opioid Receptor (MOR) providing the only effective treatment for chronic pain patients. These studies explore three pre-clinical… (more)

Subjects/Keywords: Bivalent; Delta Opioid Receptor; Functional Selectivity; MDOR Heterodimer; Mu Opioid Receptor; Opioid Signaling

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APA (6th Edition):

Olson, K. M. (2017). Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/626669

Chicago Manual of Style (16th Edition):

Olson, Keith Mathew. “Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling .” 2017. Doctoral Dissertation, University of Arizona. Accessed December 09, 2019. http://hdl.handle.net/10150/626669.

MLA Handbook (7th Edition):

Olson, Keith Mathew. “Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling .” 2017. Web. 09 Dec 2019.

Vancouver:

Olson KM. Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling . [Internet] [Doctoral dissertation]. University of Arizona; 2017. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/10150/626669.

Council of Science Editors:

Olson KM. Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling . [Doctoral Dissertation]. University of Arizona; 2017. Available from: http://hdl.handle.net/10150/626669

6. Cabana, Jérôme. Étude des déterminants structuraux de l'activation des voies de signalisation de la protéine G[indice inférieur q/11] et des β-arrestines par le récepteur de type 1 à l'angiotensine II.

Degree: PhD, Pharmacologie, 2015, Université de Sherbrooke

 Résumé : La signalisation biaisée représente la capacité des récepteurs couplés aux protéines G (RCPG) d'engager des voies de signalisation distinctes avec des efficacités variables… (more)

Subjects/Keywords: RCPG; GPCR; Récepteur AT1; Mécanisme d'activation; Sélectivité fonctionnelle; Signalisation biaisée; Angiotensine II; Dynamique moléculaire; AT1 receptor; Activation mechanism; Angiotensin II; Biased signaling; Functional selectivity; Molecular dynamics

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APA (6th Edition):

Cabana, J. (2015). Étude des déterminants structuraux de l'activation des voies de signalisation de la protéine G[indice inférieur q/11] et des β-arrestines par le récepteur de type 1 à l'angiotensine II. (Doctoral Dissertation). Université de Sherbrooke. Retrieved from http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_7706.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/7706/4/Cabana_Jerome_PhD_2015.pdf

Chicago Manual of Style (16th Edition):

Cabana, Jérôme. “Étude des déterminants structuraux de l'activation des voies de signalisation de la protéine G[indice inférieur q/11] et des β-arrestines par le récepteur de type 1 à l'angiotensine II.” 2015. Doctoral Dissertation, Université de Sherbrooke. Accessed December 09, 2019. http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_7706.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/7706/4/Cabana_Jerome_PhD_2015.pdf.

MLA Handbook (7th Edition):

Cabana, Jérôme. “Étude des déterminants structuraux de l'activation des voies de signalisation de la protéine G[indice inférieur q/11] et des β-arrestines par le récepteur de type 1 à l'angiotensine II.” 2015. Web. 09 Dec 2019.

Vancouver:

Cabana J. Étude des déterminants structuraux de l'activation des voies de signalisation de la protéine G[indice inférieur q/11] et des β-arrestines par le récepteur de type 1 à l'angiotensine II. [Internet] [Doctoral dissertation]. Université de Sherbrooke; 2015. [cited 2019 Dec 09]. Available from: http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_7706.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/7706/4/Cabana_Jerome_PhD_2015.pdf.

Council of Science Editors:

Cabana J. Étude des déterminants structuraux de l'activation des voies de signalisation de la protéine G[indice inférieur q/11] et des β-arrestines par le récepteur de type 1 à l'angiotensine II. [Doctoral Dissertation]. Université de Sherbrooke; 2015. Available from: http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_7706.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/7706/4/Cabana_Jerome_PhD_2015.pdf


Université de Montréal

7. Trottier, Giacomo. The biasing of the 5-HT4 receptor as an antidepressant target .

Degree: 2017, Université de Montréal

 La dépression majeure peut être très dommageable pour le 8% des Nord-Américains qui en souffriront au moins une fois durant leur vie. Les traitements actuels… (more)

Subjects/Keywords: 5-HT; RS67333; BRET; AD; Antidepressant; pCREB; CREB; Anhedonia; Zacopride; Prucalopride; ML10302; 5-HT4; Functional Selectivity; anhédonie; GPCR; récepteur 5-HT4; 5-HT4 Receptor; Sélectivité Fonctionnelle

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APA (6th Edition):

Trottier, G. (2017). The biasing of the 5-HT4 receptor as an antidepressant target . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/18903

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):

Trottier, Giacomo. “The biasing of the 5-HT4 receptor as an antidepressant target .” 2017. Thesis, Université de Montréal. Accessed December 09, 2019. http://hdl.handle.net/1866/18903.

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

MLA Handbook (7th Edition):

Trottier, Giacomo. “The biasing of the 5-HT4 receptor as an antidepressant target .” 2017. Web. 09 Dec 2019.

Vancouver:

Trottier G. The biasing of the 5-HT4 receptor as an antidepressant target . [Internet] [Thesis]. Université de Montréal; 2017. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/1866/18903.

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

Council of Science Editors:

Trottier G. The biasing of the 5-HT4 receptor as an antidepressant target . [Thesis]. Université de Montréal; 2017. Available from: http://hdl.handle.net/1866/18903

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


Université de Sherbrooke

8. Cabana, Jérôme. Étude des déterminants structuraux de l'activation des voies de signalisation de la protéine G[indice inférieur q/11] et des β-arrestines par le récepteur de type 1 à l'angiotensine II .

Degree: 2015, Université de Sherbrooke

 Résumé : La signalisation biaisée représente la capacité des récepteurs couplés aux protéines G (RCPG) d'engager des voies de signalisation distinctes avec des efficacités variables… (more)

Subjects/Keywords: RCPG; GPCR; Récepteur AT1; Mécanisme d'activation; Sélectivité fonctionnelle; Signalisation biaisée; Angiotensine II; Dynamique moléculaire; AT1 receptor; Activation mechanism; Angiotensin II; Biased signaling; Functional selectivity; Molecular dynamics

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APA (6th Edition):

Cabana, J. (2015). Étude des déterminants structuraux de l'activation des voies de signalisation de la protéine G[indice inférieur q/11] et des β-arrestines par le récepteur de type 1 à l'angiotensine II . (Doctoral Dissertation). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/7706

Chicago Manual of Style (16th Edition):

Cabana, Jérôme. “Étude des déterminants structuraux de l'activation des voies de signalisation de la protéine G[indice inférieur q/11] et des β-arrestines par le récepteur de type 1 à l'angiotensine II .” 2015. Doctoral Dissertation, Université de Sherbrooke. Accessed December 09, 2019. http://hdl.handle.net/11143/7706.

MLA Handbook (7th Edition):

Cabana, Jérôme. “Étude des déterminants structuraux de l'activation des voies de signalisation de la protéine G[indice inférieur q/11] et des β-arrestines par le récepteur de type 1 à l'angiotensine II .” 2015. Web. 09 Dec 2019.

Vancouver:

Cabana J. Étude des déterminants structuraux de l'activation des voies de signalisation de la protéine G[indice inférieur q/11] et des β-arrestines par le récepteur de type 1 à l'angiotensine II . [Internet] [Doctoral dissertation]. Université de Sherbrooke; 2015. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/11143/7706.

Council of Science Editors:

Cabana J. Étude des déterminants structuraux de l'activation des voies de signalisation de la protéine G[indice inférieur q/11] et des β-arrestines par le récepteur de type 1 à l'angiotensine II . [Doctoral Dissertation]. Université de Sherbrooke; 2015. Available from: http://hdl.handle.net/11143/7706

9. Nattino, Francesco. Ab initio molecular dynamics calculations on reactions of molecules with metal surfaces.

Degree: 2015, Theoretical Chemistry Group, Leiden Institute of Chemistry (LIC), Faculty of Science, Leiden University

 Reactions on metal surfaces are of scientific interest due to the tremendous relevance of heterogeneous catalysis. Single crystal surfaces under controlled physical conditions are generally… (more)

Subjects/Keywords: Ab-initio-molecular-dynamics; Density-functional-theory; Gas-surface dynamics; Surface-temperature effects; Mode specificity; Bond selectivity; Ab-initio-molecular-dynamics; Density-functional-theory; Gas-surface dynamics; Surface-temperature effects; Mode specificity; Bond selectivity

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APA (6th Edition):

Nattino, F. (2015). Ab initio molecular dynamics calculations on reactions of molecules with metal surfaces. (Doctoral Dissertation). Theoretical Chemistry Group, Leiden Institute of Chemistry (LIC), Faculty of Science, Leiden University. Retrieved from http://hdl.handle.net/1887/35980

Chicago Manual of Style (16th Edition):

Nattino, Francesco. “Ab initio molecular dynamics calculations on reactions of molecules with metal surfaces.” 2015. Doctoral Dissertation, Theoretical Chemistry Group, Leiden Institute of Chemistry (LIC), Faculty of Science, Leiden University. Accessed December 09, 2019. http://hdl.handle.net/1887/35980.

MLA Handbook (7th Edition):

Nattino, Francesco. “Ab initio molecular dynamics calculations on reactions of molecules with metal surfaces.” 2015. Web. 09 Dec 2019.

Vancouver:

Nattino F. Ab initio molecular dynamics calculations on reactions of molecules with metal surfaces. [Internet] [Doctoral dissertation]. Theoretical Chemistry Group, Leiden Institute of Chemistry (LIC), Faculty of Science, Leiden University; 2015. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/1887/35980.

Council of Science Editors:

Nattino F. Ab initio molecular dynamics calculations on reactions of molecules with metal surfaces. [Doctoral Dissertation]. Theoretical Chemistry Group, Leiden Institute of Chemistry (LIC), Faculty of Science, Leiden University; 2015. Available from: http://hdl.handle.net/1887/35980


Université de Montréal

10. Lagréou, Alexandre. À la recherche de meilleurs traitements analgésiques : interactions entre le récepteur opioïde δ et ses différents agonistes .

Degree: 2017, Université de Montréal

 Les opioïdes restent encore à l’heure actuelle les composés pharmacologiques les plus efficaces pour traiter les différentes formes de douleurs, et donc fournir une analgésie… (more)

Subjects/Keywords: Récepteurs couplés aux protéines G; RCPG; Sélectivité fonctionnelle; Analgésie; Biais; Convulsions; Modèle opérationnel; G protein-coupled receptor; GPCR; Bioluminescence resonance energy transfer; BRET; Delta opioid receptor; Récepteur opioïde delta; DOP; Analgesia; Functional selectivity; Transfert d'énergie de bioluminescence par résonance; Biased agonism; Seizures; Operational model

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APA (6th Edition):

Lagréou, A. (2017). À la recherche de meilleurs traitements analgésiques : interactions entre le récepteur opioïde δ et ses différents agonistes . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/18900

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):

Lagréou, Alexandre. “À la recherche de meilleurs traitements analgésiques : interactions entre le récepteur opioïde δ et ses différents agonistes .” 2017. Thesis, Université de Montréal. Accessed December 09, 2019. http://hdl.handle.net/1866/18900.

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

MLA Handbook (7th Edition):

Lagréou, Alexandre. “À la recherche de meilleurs traitements analgésiques : interactions entre le récepteur opioïde δ et ses différents agonistes .” 2017. Web. 09 Dec 2019.

Vancouver:

Lagréou A. À la recherche de meilleurs traitements analgésiques : interactions entre le récepteur opioïde δ et ses différents agonistes . [Internet] [Thesis]. Université de Montréal; 2017. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/1866/18900.

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

Council of Science Editors:

Lagréou A. À la recherche de meilleurs traitements analgésiques : interactions entre le récepteur opioïde δ et ses différents agonistes . [Thesis]. Université de Montréal; 2017. Available from: http://hdl.handle.net/1866/18900

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

11. Gabl, Michael. Modulation of Receptor Signaling and Functional Selectivity in Neutrophils.

Degree: 2017, University of Gothenburg / Göteborgs Universitet

 Neutrophils are important effector cells of the innate immune system and in the regulation of inflammation. Many of their functions, such as chemotactic migration, secretion… (more)

Subjects/Keywords: neutrophils; G-protein coupled receptors; reactive oxygen species; ligands; functional selectivity; allosteric modulation

…56 Functional Selectivity… …certain morphological and functional changes and they are transferred from a resting to a primed… …TLR11 is a non-functional pseudogene and TLR12 and 13 are lacking [80]. Human… 

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APA (6th Edition):

Gabl, M. (2017). Modulation of Receptor Signaling and Functional Selectivity in Neutrophils. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/52860

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):

Gabl, Michael. “Modulation of Receptor Signaling and Functional Selectivity in Neutrophils.” 2017. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed December 09, 2019. http://hdl.handle.net/2077/52860.

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

MLA Handbook (7th Edition):

Gabl, Michael. “Modulation of Receptor Signaling and Functional Selectivity in Neutrophils.” 2017. Web. 09 Dec 2019.

Vancouver:

Gabl M. Modulation of Receptor Signaling and Functional Selectivity in Neutrophils. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2017. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/2077/52860.

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

Council of Science Editors:

Gabl M. Modulation of Receptor Signaling and Functional Selectivity in Neutrophils. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2017. Available from: http://hdl.handle.net/2077/52860

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

12. Martí Solano, Maria. Ligand selectivity at GPCRs: from multitarget binding profiles to biased agonism.

Degree: Departament de Ciències Experimentals i de la Salut, 2015, Universitat Pompeu Fabra

 Deeper characterization of drugs targeting G protein-coupled receptors (GPCR)s has shown that their mechanisms of action can be more complex than previously thought. On the… (more)

Subjects/Keywords: GPCR; Afinitat d’unió; Selectivitat funcional; Serotonina; Farmacoinformàtica; Binding affinity; Functional selectivity; Serotonin; Pharmacoinformatics; 615

…pathway or functional selectivity and analyze its potential impact in different therapeutic… …functional selectivity at the 2A serotonin receptor, an important antipsychotic drug target… …receptors: implications for functional selectivity 173 xv 3.5 Detection of new biased agonists… …with wanted and unwanted effects. 4 1.3 Functional selectivity and its therapeutic… …different type of selectivity, namely functional selectivity. Functional selectivity is a property… 

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APA (6th Edition):

Martí Solano, M. (2015). Ligand selectivity at GPCRs: from multitarget binding profiles to biased agonism. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/285964

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):

Martí Solano, Maria. “Ligand selectivity at GPCRs: from multitarget binding profiles to biased agonism.” 2015. Thesis, Universitat Pompeu Fabra. Accessed December 09, 2019. http://hdl.handle.net/10803/285964.

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

MLA Handbook (7th Edition):

Martí Solano, Maria. “Ligand selectivity at GPCRs: from multitarget binding profiles to biased agonism.” 2015. Web. 09 Dec 2019.

Vancouver:

Martí Solano M. Ligand selectivity at GPCRs: from multitarget binding profiles to biased agonism. [Internet] [Thesis]. Universitat Pompeu Fabra; 2015. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/10803/285964.

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

Council of Science Editors:

Martí Solano M. Ligand selectivity at GPCRs: from multitarget binding profiles to biased agonism. [Thesis]. Universitat Pompeu Fabra; 2015. Available from: http://hdl.handle.net/10803/285964

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

13. Peterson, Sean Michael. Functional Selectivity at the Dopamine D2 Receptor .

Degree: 2015, Duke University

  The neuromodulator dopamine signals through the dopamine D2 receptor (D2R) to modulate central nervous system functions through diverse signal transduction pathways. D2R is a… (more)

Subjects/Keywords: Cellular biology; Pharmacology; Dopamine; Functional Selectivity; GPCR; G protein; β-arrestin

…36 Table II: Evolutionary Action predicted functional selectivity phenotype mutations in… …91 Table IV: Receptor manipulations yield operationally defined functional selectivity… …Ligand contributions to functional selectivity. Calculated from Figures 9 and 10. *p<0.05 when… …Table VI: Transducer contributions to functional selectivity. Calculated from Figure 11. *p… …94 viii List of Figures Figure 1: The functional selectivity of D2R. (A)… 

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

APA (6th Edition):

Peterson, S. M. (2015). Functional Selectivity at the Dopamine D2 Receptor . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/10500

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):

Peterson, Sean Michael. “Functional Selectivity at the Dopamine D2 Receptor .” 2015. Thesis, Duke University. Accessed December 09, 2019. http://hdl.handle.net/10161/10500.

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

MLA Handbook (7th Edition):

Peterson, Sean Michael. “Functional Selectivity at the Dopamine D2 Receptor .” 2015. Web. 09 Dec 2019.

Vancouver:

Peterson SM. Functional Selectivity at the Dopamine D2 Receptor . [Internet] [Thesis]. Duke University; 2015. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/10161/10500.

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

Council of Science Editors:

Peterson SM. Functional Selectivity at the Dopamine D2 Receptor . [Thesis]. Duke University; 2015. Available from: http://hdl.handle.net/10161/10500

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


Université de Montréal

14. Charfi, Iness. Étude des propriétés de signalisation et de trafic du récepteur delta opiacé : vers une meilleure compréhension des bases cellulaires de la tolérance analgésique aux opioïdes .

Degree: 2018, Université de Montréal

Subjects/Keywords: RCPG; DOPr; Signalisation; Internalisation; Sélectivité fonctionnelle; Modèle opérationnel; Recyclage; TGN; Rab9; TIP47; ALIX; Tolérance analgésique; GPCR; Signaling; Internalization; Functional selectivity; Operational model; Recycling; Analgesic tolerance

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

APA (6th Edition):

Charfi, I. (2018). Étude des propriétés de signalisation et de trafic du récepteur delta opiacé : vers une meilleure compréhension des bases cellulaires de la tolérance analgésique aux opioïdes . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/21203

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):

Charfi, Iness. “Étude des propriétés de signalisation et de trafic du récepteur delta opiacé : vers une meilleure compréhension des bases cellulaires de la tolérance analgésique aux opioïdes .” 2018. Thesis, Université de Montréal. Accessed December 09, 2019. http://hdl.handle.net/1866/21203.

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

MLA Handbook (7th Edition):

Charfi, Iness. “Étude des propriétés de signalisation et de trafic du récepteur delta opiacé : vers une meilleure compréhension des bases cellulaires de la tolérance analgésique aux opioïdes .” 2018. Web. 09 Dec 2019.

Vancouver:

Charfi I. Étude des propriétés de signalisation et de trafic du récepteur delta opiacé : vers une meilleure compréhension des bases cellulaires de la tolérance analgésique aux opioïdes . [Internet] [Thesis]. Université de Montréal; 2018. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/1866/21203.

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

Council of Science Editors:

Charfi I. Étude des propriétés de signalisation et de trafic du récepteur delta opiacé : vers une meilleure compréhension des bases cellulaires de la tolérance analgésique aux opioïdes . [Thesis]. Université de Montréal; 2018. Available from: http://hdl.handle.net/1866/21203

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


Université de Montréal

15. Nadeau-Vallée, Mathieu. Regulation of Interleukin-1 governs acute intrauterine inflammation to improve gestational and neonatal outcome .

Degree: 2019, Université de Montréal

Subjects/Keywords: Naissance prématurée; Travail préterme; Interleukine-1; Anti-IL-1; Inflammation; Morbidité néonatale; Sélectivité fonctionnelle; Lactate; GPR81; Preterm birth; Preterm labor; Interleukin-1; Neonatal morbidity; Functional selectivity

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APA (6th Edition):

Nadeau-Vallée, M. (2019). Regulation of Interleukin-1 governs acute intrauterine inflammation to improve gestational and neonatal outcome . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/22598

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):

Nadeau-Vallée, Mathieu. “Regulation of Interleukin-1 governs acute intrauterine inflammation to improve gestational and neonatal outcome .” 2019. Thesis, Université de Montréal. Accessed December 09, 2019. http://hdl.handle.net/1866/22598.

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

MLA Handbook (7th Edition):

Nadeau-Vallée, Mathieu. “Regulation of Interleukin-1 governs acute intrauterine inflammation to improve gestational and neonatal outcome .” 2019. Web. 09 Dec 2019.

Vancouver:

Nadeau-Vallée M. Regulation of Interleukin-1 governs acute intrauterine inflammation to improve gestational and neonatal outcome . [Internet] [Thesis]. Université de Montréal; 2019. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/1866/22598.

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

Council of Science Editors:

Nadeau-Vallée M. Regulation of Interleukin-1 governs acute intrauterine inflammation to improve gestational and neonatal outcome . [Thesis]. Université de Montréal; 2019. Available from: http://hdl.handle.net/1866/22598

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


Vrije Universiteit Amsterdam

16. Kooistra, A.J. In silico Medicinal Chemistry: Investigating GPCRs: key regulators of signal transduction and cell function .

Degree: 2015, Vrije Universiteit Amsterdam

Subjects/Keywords: GPCRs; virtual screening; membrane proteins; transmembrane proteins; computer-aided drug design; chemogenomics; functional selectivity; histamine receptor; adrenoceptor; antihistamine; site-directed mutagenesis; structure-affinity relationship; protein-ligand interactions; GPCR crystal structures

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

APA (6th Edition):

Kooistra, A. J. (2015). In silico Medicinal Chemistry: Investigating GPCRs: key regulators of signal transduction and cell function . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/52308

Chicago Manual of Style (16th Edition):

Kooistra, A J. “In silico Medicinal Chemistry: Investigating GPCRs: key regulators of signal transduction and cell function .” 2015. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed December 09, 2019. http://hdl.handle.net/1871/52308.

MLA Handbook (7th Edition):

Kooistra, A J. “In silico Medicinal Chemistry: Investigating GPCRs: key regulators of signal transduction and cell function .” 2015. Web. 09 Dec 2019.

Vancouver:

Kooistra AJ. In silico Medicinal Chemistry: Investigating GPCRs: key regulators of signal transduction and cell function . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2015. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/1871/52308.

Council of Science Editors:

Kooistra AJ. In silico Medicinal Chemistry: Investigating GPCRs: key regulators of signal transduction and cell function . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2015. Available from: http://hdl.handle.net/1871/52308

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