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You searched for subject:( Biased agonism). Showing records 1 – 6 of 6 total matches.

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

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 15, 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. 15 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 15]. 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/ ;


Duke University

2. WANG, JIALU. Identifying Molecular Mechanisms of beta-arrestin Biased G Protein-Coupled Receptor Signaling .

Degree: 2017, Duke University

  G protein-coupled receptors (GPCRs) represent the largest and the most versatile family of cell surface receptors. Members of this receptor family translate diverse extracellular… (more)

Subjects/Keywords: Cellular biology; Molecular biology; Biochemistry; beta-arrestin; biased agonism; G protein; G protein-coupled receptor; mechanoactivation

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APA (6th Edition):

WANG, J. (2017). Identifying Molecular Mechanisms of beta-arrestin Biased G Protein-Coupled Receptor Signaling . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/16300

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):

WANG, JIALU. “Identifying Molecular Mechanisms of beta-arrestin Biased G Protein-Coupled Receptor Signaling .” 2017. Thesis, Duke University. Accessed December 15, 2019. http://hdl.handle.net/10161/16300.

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

MLA Handbook (7th Edition):

WANG, JIALU. “Identifying Molecular Mechanisms of beta-arrestin Biased G Protein-Coupled Receptor Signaling .” 2017. Web. 15 Dec 2019.

Vancouver:

WANG J. Identifying Molecular Mechanisms of beta-arrestin Biased G Protein-Coupled Receptor Signaling . [Internet] [Thesis]. Duke University; 2017. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/10161/16300.

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

Council of Science Editors:

WANG J. Identifying Molecular Mechanisms of beta-arrestin Biased G Protein-Coupled Receptor Signaling . [Thesis]. Duke University; 2017. Available from: http://hdl.handle.net/10161/16300

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


Duke University

3. Choi, Minjung. Biased Signaling at the β2-adrenergic Receptor is established by Receptor-Transducer Interactions .

Degree: 2018, Duke University

  β-Adrenergic receptors (βAR) are one of the key modulators of cardio-pulmonary functions and belong to a large family of membrane proteins, termed as G-protein… (more)

Subjects/Keywords: Biochemistry; Pharmacology; Cellular biology; Adrenergic receptor; Arrestin; Biased Agonism; GPCR kinase; G protein coupled receptor; Receptor pharmacology

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

APA (6th Edition):

Choi, M. (2018). Biased Signaling at the β2-adrenergic Receptor is established by Receptor-Transducer Interactions . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/16923

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):

Choi, Minjung. “Biased Signaling at the β2-adrenergic Receptor is established by Receptor-Transducer Interactions .” 2018. Thesis, Duke University. Accessed December 15, 2019. http://hdl.handle.net/10161/16923.

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

MLA Handbook (7th Edition):

Choi, Minjung. “Biased Signaling at the β2-adrenergic Receptor is established by Receptor-Transducer Interactions .” 2018. Web. 15 Dec 2019.

Vancouver:

Choi M. Biased Signaling at the β2-adrenergic Receptor is established by Receptor-Transducer Interactions . [Internet] [Thesis]. Duke University; 2018. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/10161/16923.

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

Council of Science Editors:

Choi M. Biased Signaling at the β2-adrenergic Receptor is established by Receptor-Transducer Interactions . [Thesis]. Duke University; 2018. Available from: http://hdl.handle.net/10161/16923

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


University of Michigan

4. Griggs, Nicholas. Bifunctional Opioid Peptidomimetics: Studies on Affinity and Efficacy.

Degree: PhD, Pharmacology, 2019, University of Michigan

 Opioids are effectively used for the treatment of acute and chronic pain, however, serious problems such as fatal overdose due to respiratory depression and opioid… (more)

Subjects/Keywords: Opioid Drugs; Opioid Receptors; Radioligand Binding; Biased Agonism; Structure-Activity Relationships; Molecular, Cellular and Developmental Biology; Science

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

APA (6th Edition):

Griggs, N. (2019). Bifunctional Opioid Peptidomimetics: Studies on Affinity and Efficacy. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/151415

Chicago Manual of Style (16th Edition):

Griggs, Nicholas. “Bifunctional Opioid Peptidomimetics: Studies on Affinity and Efficacy.” 2019. Doctoral Dissertation, University of Michigan. Accessed December 15, 2019. http://hdl.handle.net/2027.42/151415.

MLA Handbook (7th Edition):

Griggs, Nicholas. “Bifunctional Opioid Peptidomimetics: Studies on Affinity and Efficacy.” 2019. Web. 15 Dec 2019.

Vancouver:

Griggs N. Bifunctional Opioid Peptidomimetics: Studies on Affinity and Efficacy. [Internet] [Doctoral dissertation]. University of Michigan; 2019. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/2027.42/151415.

Council of Science Editors:

Griggs N. Bifunctional Opioid Peptidomimetics: Studies on Affinity and Efficacy. [Doctoral Dissertation]. University of Michigan; 2019. Available from: http://hdl.handle.net/2027.42/151415


Université de Montréal

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

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 15, 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. 15 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 15]. 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

6. Strachan, Ryan Thomas. P90 Ribosomal S6 Kinase 2 (RSK2) Directly Phosphorylates the 5-HT2A Serotonin Receptor thereby Modulating Signaling.

Degree: PhD, Biochemistry, 2009, Case Western Reserve University

 Given the pivotal role G protein-coupled receptors (GPCRs) play in physiological responses, various mechanisms have evolved to ensure the tight regulation of GPCR signaling. Classically,… (more)

Subjects/Keywords: Biochemistry; Pharmacology; serotonin; 5-HT; 5-HT2A; GPCR; RSK; ERK; phosphorylation; RTK; growth factor; functional selectivity; biased agonism

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

APA (6th Edition):

Strachan, R. T. (2009). P90 Ribosomal S6 Kinase 2 (RSK2) Directly Phosphorylates the 5-HT2A Serotonin Receptor thereby Modulating Signaling. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1247172805

Chicago Manual of Style (16th Edition):

Strachan, Ryan Thomas. “P90 Ribosomal S6 Kinase 2 (RSK2) Directly Phosphorylates the 5-HT2A Serotonin Receptor thereby Modulating Signaling.” 2009. Doctoral Dissertation, Case Western Reserve University. Accessed December 15, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1247172805.

MLA Handbook (7th Edition):

Strachan, Ryan Thomas. “P90 Ribosomal S6 Kinase 2 (RSK2) Directly Phosphorylates the 5-HT2A Serotonin Receptor thereby Modulating Signaling.” 2009. Web. 15 Dec 2019.

Vancouver:

Strachan RT. P90 Ribosomal S6 Kinase 2 (RSK2) Directly Phosphorylates the 5-HT2A Serotonin Receptor thereby Modulating Signaling. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2009. [cited 2019 Dec 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1247172805.

Council of Science Editors:

Strachan RT. P90 Ribosomal S6 Kinase 2 (RSK2) Directly Phosphorylates the 5-HT2A Serotonin Receptor thereby Modulating Signaling. [Doctoral Dissertation]. Case Western Reserve University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1247172805

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