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You searched for subject:(Biased signaling). Showing records 1 – 12 of 12 total matches.

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1. A. Vacchini. ANALYSIS OF BIASED SIGNALING IN THE CHEMOKINE SYSTEM.

Degree: 2016, Università degli Studi di Milano

 Chemokines constitute a family of almost 50 small secreted cytokines, recognized by about 20 different 7TM spanning G protein coupled receptors (GPCRs), that activating pertussis… (more)

Subjects/Keywords: Chemokine; Atypical Chemokine Receptor; Biased Signaling; Settore MED/04 - Patologia Generale

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

APA (6th Edition):

Vacchini, A. (2016). ANALYSIS OF BIASED SIGNALING IN THE CHEMOKINE SYSTEM. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/365864

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):

Vacchini, A.. “ANALYSIS OF BIASED SIGNALING IN THE CHEMOKINE SYSTEM.” 2016. Thesis, Università degli Studi di Milano. Accessed December 10, 2019. http://hdl.handle.net/2434/365864.

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

MLA Handbook (7th Edition):

Vacchini, A.. “ANALYSIS OF BIASED SIGNALING IN THE CHEMOKINE SYSTEM.” 2016. Web. 10 Dec 2019.

Vancouver:

Vacchini A. ANALYSIS OF BIASED SIGNALING IN THE CHEMOKINE SYSTEM. [Internet] [Thesis]. Università degli Studi di Milano; 2016. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/2434/365864.

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

Council of Science Editors:

Vacchini A. ANALYSIS OF BIASED SIGNALING IN THE CHEMOKINE SYSTEM. [Thesis]. Università degli Studi di Milano; 2016. Available from: http://hdl.handle.net/2434/365864

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


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 10, 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. 10 Dec 2019.

Vancouver:

Brust Fernandes T. FUNCTIONAL SELECTIVITY DOWNSTREAM OF Gαi/o-COUPLED RECEPTORS. [Internet] [Doctoral dissertation]. Purdue University; 2015. [cited 2019 Dec 10]. 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


Duke University

3. Smith, Jeffrey. Physiological Functions of Biased Signaling at the Chemokine Receptor CXCR3 .

Degree: 2019, Duke University

  G protein-coupled receptors (GPCRs) are the largest class of receptors in the human genome and one of the most common drug targets. It is… (more)

Subjects/Keywords: Biochemistry; Cellular biology; Pharmacology; Biased signaling; Chemokine; GPCR; Signal transduction

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APA (6th Edition):

Smith, J. (2019). Physiological Functions of Biased Signaling at the Chemokine Receptor CXCR3 . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/18643

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):

Smith, Jeffrey. “Physiological Functions of Biased Signaling at the Chemokine Receptor CXCR3 .” 2019. Thesis, Duke University. Accessed December 10, 2019. http://hdl.handle.net/10161/18643.

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

MLA Handbook (7th Edition):

Smith, Jeffrey. “Physiological Functions of Biased Signaling at the Chemokine Receptor CXCR3 .” 2019. Web. 10 Dec 2019.

Vancouver:

Smith J. Physiological Functions of Biased Signaling at the Chemokine Receptor CXCR3 . [Internet] [Thesis]. Duke University; 2019. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/10161/18643.

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

Council of Science Editors:

Smith J. Physiological Functions of Biased Signaling at the Chemokine Receptor CXCR3 . [Thesis]. Duke University; 2019. Available from: http://hdl.handle.net/10161/18643

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

4. Santos, Geisa Aparecida dos. Análise comparativa de perfis de sinalização do receptor AT1 ativado por agonistas seletivos para a via de -arrestinas.

Degree: Mestrado, Bioquímica, 2013, University of São Paulo

Os receptores acoplados à proteína G (GPCRs), também chamados de receptores 7TM, são conhecidos por regular virtualmente todos os processos fisiológicos em mamíferos e cerca… (more)

Subjects/Keywords: Agonismo seletivo; AT1 receptor.; Biased agonism; GPCR; GPCR; Receptor AT1.; Signaling; Sinalização

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APA (6th Edition):

Santos, G. A. d. (2013). Análise comparativa de perfis de sinalização do receptor AT1 ativado por agonistas seletivos para a via de -arrestinas. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/17/17131/tde-31102013-150124/ ;

Chicago Manual of Style (16th Edition):

Santos, Geisa Aparecida dos. “Análise comparativa de perfis de sinalização do receptor AT1 ativado por agonistas seletivos para a via de -arrestinas.” 2013. Masters Thesis, University of São Paulo. Accessed December 10, 2019. http://www.teses.usp.br/teses/disponiveis/17/17131/tde-31102013-150124/ ;.

MLA Handbook (7th Edition):

Santos, Geisa Aparecida dos. “Análise comparativa de perfis de sinalização do receptor AT1 ativado por agonistas seletivos para a via de -arrestinas.” 2013. Web. 10 Dec 2019.

Vancouver:

Santos GAd. Análise comparativa de perfis de sinalização do receptor AT1 ativado por agonistas seletivos para a via de -arrestinas. [Internet] [Masters thesis]. University of São Paulo; 2013. [cited 2019 Dec 10]. Available from: http://www.teses.usp.br/teses/disponiveis/17/17131/tde-31102013-150124/ ;.

Council of Science Editors:

Santos GAd. Análise comparativa de perfis de sinalização do receptor AT1 ativado por agonistas seletivos para a via de -arrestinas. [Masters Thesis]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/17/17131/tde-31102013-150124/ ;


Université de Sherbrooke

5. St-Pierre, David. Mécanismes de signalisation d’AT1R médiés par des analogues cycliques de l’angiotensine II .

Degree: 2017, Université de Sherbrooke

 L'angiotensine II (Ang II) joue un rôle important dans la régulation du système cardiovasculaire par l’activation de plusieurs voies de signalisation. L’activation de ces voies… (more)

Subjects/Keywords: AT1R; Angiotensine II; Signalisation biaisée; Analogues cycliques; Angiotensin II; Biased signaling; Cyclic analogs

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APA (6th Edition):

St-Pierre, D. (2017). Mécanismes de signalisation d’AT1R médiés par des analogues cycliques de l’angiotensine II . (Masters Thesis). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/11091

Chicago Manual of Style (16th Edition):

St-Pierre, David. “Mécanismes de signalisation d’AT1R médiés par des analogues cycliques de l’angiotensine II .” 2017. Masters Thesis, Université de Sherbrooke. Accessed December 10, 2019. http://hdl.handle.net/11143/11091.

MLA Handbook (7th Edition):

St-Pierre, David. “Mécanismes de signalisation d’AT1R médiés par des analogues cycliques de l’angiotensine II .” 2017. Web. 10 Dec 2019.

Vancouver:

St-Pierre D. Mécanismes de signalisation d’AT1R médiés par des analogues cycliques de l’angiotensine II . [Internet] [Masters thesis]. Université de Sherbrooke; 2017. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/11143/11091.

Council of Science Editors:

St-Pierre D. Mécanismes de signalisation d’AT1R médiés par des analogues cycliques de l’angiotensine II . [Masters Thesis]. Université de Sherbrooke; 2017. Available from: http://hdl.handle.net/11143/11091


Université de Montréal

6. Guité-Vinet, François. CXCR3 biased signaling, heteromerization and decoy properties .

Degree: 2015, Université de Montréal

 Le récepteur de chimiokine CXCR3 est un récepteur couplé à la protéine G (RCPG) exprimé, entre autre, sur les cellules T activées lors d’une réponse… (more)

Subjects/Keywords: RCPG; Signalisation biaisée; Hétéromérisation; BRET; CXCR3; CXCR4; CXCR7; CXCL4; GPCR; Biased signaling; Heteromerization

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APA (6th Edition):

Guité-Vinet, F. (2015). CXCR3 biased signaling, heteromerization and decoy properties . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/13112

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):

Guité-Vinet, François. “CXCR3 biased signaling, heteromerization and decoy properties .” 2015. Thesis, Université de Montréal. Accessed December 10, 2019. http://hdl.handle.net/1866/13112.

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

MLA Handbook (7th Edition):

Guité-Vinet, François. “CXCR3 biased signaling, heteromerization and decoy properties .” 2015. Web. 10 Dec 2019.

Vancouver:

Guité-Vinet F. CXCR3 biased signaling, heteromerization and decoy properties . [Internet] [Thesis]. Université de Montréal; 2015. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/1866/13112.

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

Council of Science Editors:

Guité-Vinet F. CXCR3 biased signaling, heteromerization and decoy properties . [Thesis]. Université de Montréal; 2015. Available from: http://hdl.handle.net/1866/13112

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


University of Houston

7. Forkuo, Gloria S. The Role of the Canonical Beta-2 Adrenoceptor Gs Pathway in Development of the Asthma Phenotype in Murine Models.

Degree: Pharmacological and Pharmaceutical Sciences, Department of, 2014, University of Houston

 Asthma is a chronic inflammatory disease of the airways characterized by variable degrees of inflammation, mucous metaplasia and airway hyperresponsiveness (AHR). Asthma causes over a… (more)

Subjects/Keywords: Asthma; β2AR agonists; biased signaling; Gs-cAMP; formoterol; salmeterol; PDEs; PDE4 inhibitors

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APA (6th Edition):

Forkuo, G. S. (2014). The Role of the Canonical Beta-2 Adrenoceptor Gs Pathway in Development of the Asthma Phenotype in Murine Models. (Thesis). University of Houston. Retrieved from http://hdl.handle.net/10657/3644

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):

Forkuo, Gloria S. “The Role of the Canonical Beta-2 Adrenoceptor Gs Pathway in Development of the Asthma Phenotype in Murine Models.” 2014. Thesis, University of Houston. Accessed December 10, 2019. http://hdl.handle.net/10657/3644.

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

MLA Handbook (7th Edition):

Forkuo, Gloria S. “The Role of the Canonical Beta-2 Adrenoceptor Gs Pathway in Development of the Asthma Phenotype in Murine Models.” 2014. Web. 10 Dec 2019.

Vancouver:

Forkuo GS. The Role of the Canonical Beta-2 Adrenoceptor Gs Pathway in Development of the Asthma Phenotype in Murine Models. [Internet] [Thesis]. University of Houston; 2014. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/10657/3644.

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

Council of Science Editors:

Forkuo GS. The Role of the Canonical Beta-2 Adrenoceptor Gs Pathway in Development of the Asthma Phenotype in Murine Models. [Thesis]. University of Houston; 2014. Available from: http://hdl.handle.net/10657/3644

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


Universitat Autònoma de Barcelona

8. Zhou, Bin. Mathematical modeling of oligomerization and biased signaling of G-protein-coupled receptors.

Degree: 2018, Universitat Autònoma de Barcelona

 G-protein-coupled receptors (GPCRs) play very important roles in a great variety of biological processes. They are located in the membrane and mediate the signaling pathways… (more)

Subjects/Keywords: Modelització matemàtica; Modelización matemática; Mathematical modeling; Oligomerització; Oligomerización; Oligomerization; Senyalització esbiaixada; Señalización sesgada; Biased signaling; Ciències de la Salut; 615

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APA (6th Edition):

Zhou, B. (2018). Mathematical modeling of oligomerization and biased signaling of G-protein-coupled receptors. (Thesis). Universitat Autònoma de Barcelona. Retrieved from http://hdl.handle.net/10803/665141

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):

Zhou, Bin. “Mathematical modeling of oligomerization and biased signaling of G-protein-coupled receptors.” 2018. Thesis, Universitat Autònoma de Barcelona. Accessed December 10, 2019. http://hdl.handle.net/10803/665141.

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

MLA Handbook (7th Edition):

Zhou, Bin. “Mathematical modeling of oligomerization and biased signaling of G-protein-coupled receptors.” 2018. Web. 10 Dec 2019.

Vancouver:

Zhou B. Mathematical modeling of oligomerization and biased signaling of G-protein-coupled receptors. [Internet] [Thesis]. Universitat Autònoma de Barcelona; 2018. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/10803/665141.

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

Council of Science Editors:

Zhou B. Mathematical modeling of oligomerization and biased signaling of G-protein-coupled receptors. [Thesis]. Universitat Autònoma de Barcelona; 2018. Available from: http://hdl.handle.net/10803/665141

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

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

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 10, 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. 10 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 10]. 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 Sherbrooke

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

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 10, 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. 10 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 10]. 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

11. Roth, S. Where is the bias? .

Degree: 2016, Vrije Universiteit Amsterdam

Subjects/Keywords: G protein-coupled receptors; ligand biased signaling; Calcium sensing receptor; mathematical modeling; fluorescent microscopy

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APA (6th Edition):

Roth, S. (2016). Where is the bias? . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/54356

Chicago Manual of Style (16th Edition):

Roth, S. “Where is the bias? .” 2016. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed December 10, 2019. http://hdl.handle.net/1871/54356.

MLA Handbook (7th Edition):

Roth, S. “Where is the bias? .” 2016. Web. 10 Dec 2019.

Vancouver:

Roth S. Where is the bias? . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2016. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/1871/54356.

Council of Science Editors:

Roth S. Where is the bias? . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2016. Available from: http://hdl.handle.net/1871/54356


Université de Montréal

12. Picard, Louis-Philippe. Déterminants structuraux et moléculaires de la sélectivité fonctionnelle du récepteur β2-adrénergique .

Degree: 2019, Université de Montréal

Subjects/Keywords: Récepteurs couplés aux protéines G (RCPGs); Récepteur β2-adrénergique (β2AR); Signalisation cellulaire; Signalisation biaisée; Structure; Biocapteur; G proteins-coupled receptors (GPCRs); β2-adrenergic receptor (β2AR); Ligand biased signaling; Biosensors; Cell signaling

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

APA (6th Edition):

Picard, L. (2019). Déterminants structuraux et moléculaires de la sélectivité fonctionnelle du récepteur β2-adrénergique . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/22524

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):

Picard, Louis-Philippe. “Déterminants structuraux et moléculaires de la sélectivité fonctionnelle du récepteur β2-adrénergique .” 2019. Thesis, Université de Montréal. Accessed December 10, 2019. http://hdl.handle.net/1866/22524.

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

MLA Handbook (7th Edition):

Picard, Louis-Philippe. “Déterminants structuraux et moléculaires de la sélectivité fonctionnelle du récepteur β2-adrénergique .” 2019. Web. 10 Dec 2019.

Vancouver:

Picard L. Déterminants structuraux et moléculaires de la sélectivité fonctionnelle du récepteur β2-adrénergique . [Internet] [Thesis]. Université de Montréal; 2019. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/1866/22524.

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

Council of Science Editors:

Picard L. Déterminants structuraux et moléculaires de la sélectivité fonctionnelle du récepteur β2-adrénergique . [Thesis]. Université de Montréal; 2019. Available from: http://hdl.handle.net/1866/22524

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

.