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You searched for subject:(GPCRs). Showing records 1 – 30 of 92 total matches.

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1. 根本, 航. Class A Gタンパク質共役型受容体がオリゴマー化する際のインターフェイスを予測する手法の開発 : Prediction of interfaces for oligomerization of class A G-protein coupled receptors; Class A G タンパクシツ キョウヤクガタ ジュヨウタイ ガ オリゴマーカ スル サイ ノ インターフェイス オ ヨソク スル シュホウ ノ カイハツ.

Degree: Nara Institute of Science and Technology / 奈良先端科学技術大学院大学

Subjects/Keywords: GPCRs; オリゴマー

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

APA (6th Edition):

根本, . (n.d.). Class A Gタンパク質共役型受容体がオリゴマー化する際のインターフェイスを予測する手法の開発 : Prediction of interfaces for oligomerization of class A G-protein coupled receptors; Class A G タンパクシツ キョウヤクガタ ジュヨウタイ ガ オリゴマーカ スル サイ ノ インターフェイス オ ヨソク スル シュホウ ノ カイハツ. (Thesis). Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Retrieved from http://hdl.handle.net/10061/2882

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

根本, 航. “Class A Gタンパク質共役型受容体がオリゴマー化する際のインターフェイスを予測する手法の開発 : Prediction of interfaces for oligomerization of class A G-protein coupled receptors; Class A G タンパクシツ キョウヤクガタ ジュヨウタイ ガ オリゴマーカ スル サイ ノ インターフェイス オ ヨソク スル シュホウ ノ カイハツ.” Thesis, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Accessed April 13, 2021. http://hdl.handle.net/10061/2882.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

根本, 航. “Class A Gタンパク質共役型受容体がオリゴマー化する際のインターフェイスを予測する手法の開発 : Prediction of interfaces for oligomerization of class A G-protein coupled receptors; Class A G タンパクシツ キョウヤクガタ ジュヨウタイ ガ オリゴマーカ スル サイ ノ インターフェイス オ ヨソク スル シュホウ ノ カイハツ.” Web. 13 Apr 2021.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

根本 . Class A Gタンパク質共役型受容体がオリゴマー化する際のインターフェイスを予測する手法の開発 : Prediction of interfaces for oligomerization of class A G-protein coupled receptors; Class A G タンパクシツ キョウヤクガタ ジュヨウタイ ガ オリゴマーカ スル サイ ノ インターフェイス オ ヨソク スル シュホウ ノ カイハツ. [Internet] [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10061/2882.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

根本 . Class A Gタンパク質共役型受容体がオリゴマー化する際のインターフェイスを予測する手法の開発 : Prediction of interfaces for oligomerization of class A G-protein coupled receptors; Class A G タンパクシツ キョウヤクガタ ジュヨウタイ ガ オリゴマーカ スル サイ ノ インターフェイス オ ヨソク スル シュホウ ノ カイハツ. [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; Available from: http://hdl.handle.net/10061/2882

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


University of Ottawa

2. Albaker, Awatif. Mutational Analysis to Define the Functional Role of the Third Intracellular Loop of D1-Class Dopaminergic Receptors .

Degree: 2016, University of Ottawa

 The third intracellular loop (IL3) and cytoplasmic tail (CT), which are the most divergent regions between human D1-class dopaminergic receptors (hD1R and hD5R), have been… (more)

Subjects/Keywords: GPCRs; D1R; D5R; IL3; Dopamine

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APA (6th Edition):

Albaker, A. (2016). Mutational Analysis to Define the Functional Role of the Third Intracellular Loop of D1-Class Dopaminergic Receptors . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/35063

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):

Albaker, Awatif. “Mutational Analysis to Define the Functional Role of the Third Intracellular Loop of D1-Class Dopaminergic Receptors .” 2016. Thesis, University of Ottawa. Accessed April 13, 2021. http://hdl.handle.net/10393/35063.

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

MLA Handbook (7th Edition):

Albaker, Awatif. “Mutational Analysis to Define the Functional Role of the Third Intracellular Loop of D1-Class Dopaminergic Receptors .” 2016. Web. 13 Apr 2021.

Vancouver:

Albaker A. Mutational Analysis to Define the Functional Role of the Third Intracellular Loop of D1-Class Dopaminergic Receptors . [Internet] [Thesis]. University of Ottawa; 2016. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10393/35063.

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

Council of Science Editors:

Albaker A. Mutational Analysis to Define the Functional Role of the Third Intracellular Loop of D1-Class Dopaminergic Receptors . [Thesis]. University of Ottawa; 2016. Available from: http://hdl.handle.net/10393/35063

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


University of Minnesota

3. Yekkirala, Ajay S. Elucidating the role of opioid receptor heteromers as targets for analgesic drug design.

Degree: PhD, Pharmacology, 2011, University of Minnesota

 Opioid receptors are class A members of the G protein coupled-receptor (GPCR) superfamily. There is high amino acid homology (~60%) within the opioid receptor family… (more)

Subjects/Keywords: Analgesics; GPCRs; Heterodimers; Opioid

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APA (6th Edition):

Yekkirala, A. S. (2011). Elucidating the role of opioid receptor heteromers as targets for analgesic drug design. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/161209

Chicago Manual of Style (16th Edition):

Yekkirala, Ajay S. “Elucidating the role of opioid receptor heteromers as targets for analgesic drug design.” 2011. Doctoral Dissertation, University of Minnesota. Accessed April 13, 2021. http://purl.umn.edu/161209.

MLA Handbook (7th Edition):

Yekkirala, Ajay S. “Elucidating the role of opioid receptor heteromers as targets for analgesic drug design.” 2011. Web. 13 Apr 2021.

Vancouver:

Yekkirala AS. Elucidating the role of opioid receptor heteromers as targets for analgesic drug design. [Internet] [Doctoral dissertation]. University of Minnesota; 2011. [cited 2021 Apr 13]. Available from: http://purl.umn.edu/161209.

Council of Science Editors:

Yekkirala AS. Elucidating the role of opioid receptor heteromers as targets for analgesic drug design. [Doctoral Dissertation]. University of Minnesota; 2011. Available from: http://purl.umn.edu/161209


Dalhousie University

4. Holland, Patrick. DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS.

Degree: MS, Department of Pharmacology, 2012, Dalhousie University

GPCRs are known to form dimeric structures, and this affects their pharmacological properties. The ?2AR and AT1aR are GPCRs that are involved the regulation of… (more)

Subjects/Keywords: GPCRs; Signalling; Polymorphism; Dimerization; Receptor Pharmacology

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APA (6th Edition):

Holland, P. (2012). DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/15245

Chicago Manual of Style (16th Edition):

Holland, Patrick. “DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS.” 2012. Masters Thesis, Dalhousie University. Accessed April 13, 2021. http://hdl.handle.net/10222/15245.

MLA Handbook (7th Edition):

Holland, Patrick. “DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS.” 2012. Web. 13 Apr 2021.

Vancouver:

Holland P. DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS. [Internet] [Masters thesis]. Dalhousie University; 2012. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10222/15245.

Council of Science Editors:

Holland P. DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS. [Masters Thesis]. Dalhousie University; 2012. Available from: http://hdl.handle.net/10222/15245


Vanderbilt University

5. Downey, Jason Duane. Structure-Function Analyses of Prostaglandin E2 Receptor Subtypes 1 and 3.

Degree: PhD, Pharmacology, 2012, Vanderbilt University

 Prostaglandin E2 (PGE2) is a lipid autacoid, which is an oxidative metabolite of arachidonic acid synthesized by cyclooxygenase and prostaglandin E synthases. PGE2 is proposed… (more)

Subjects/Keywords: hypertension; drug discovery; prostaglandin; GPCRs; diabetes

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APA (6th Edition):

Downey, J. D. (2012). Structure-Function Analyses of Prostaglandin E2 Receptor Subtypes 1 and 3. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14474

Chicago Manual of Style (16th Edition):

Downey, Jason Duane. “Structure-Function Analyses of Prostaglandin E2 Receptor Subtypes 1 and 3.” 2012. Doctoral Dissertation, Vanderbilt University. Accessed April 13, 2021. http://hdl.handle.net/1803/14474.

MLA Handbook (7th Edition):

Downey, Jason Duane. “Structure-Function Analyses of Prostaglandin E2 Receptor Subtypes 1 and 3.” 2012. Web. 13 Apr 2021.

Vancouver:

Downey JD. Structure-Function Analyses of Prostaglandin E2 Receptor Subtypes 1 and 3. [Internet] [Doctoral dissertation]. Vanderbilt University; 2012. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1803/14474.

Council of Science Editors:

Downey JD. Structure-Function Analyses of Prostaglandin E2 Receptor Subtypes 1 and 3. [Doctoral Dissertation]. Vanderbilt University; 2012. Available from: http://hdl.handle.net/1803/14474


Vanderbilt University

6. Jewell, Mark Langley. Regulation of Ca2+ channels and exocytosis by receptors for prostaglandin E2.

Degree: PhD, Pharmacology, 2013, Vanderbilt University

 Adrenal chromaffin cells release catecholamines, neuropeptides and other hormones to maintain cardiovascular and metabolic homeostasis, and tune the physiological response to acute stress. As such,… (more)

Subjects/Keywords: amperometry; PGE2; exocytosis; GPCRs; calcium channels

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APA (6th Edition):

Jewell, M. L. (2013). Regulation of Ca2+ channels and exocytosis by receptors for prostaglandin E2. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13495

Chicago Manual of Style (16th Edition):

Jewell, Mark Langley. “Regulation of Ca2+ channels and exocytosis by receptors for prostaglandin E2.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed April 13, 2021. http://hdl.handle.net/1803/13495.

MLA Handbook (7th Edition):

Jewell, Mark Langley. “Regulation of Ca2+ channels and exocytosis by receptors for prostaglandin E2.” 2013. Web. 13 Apr 2021.

Vancouver:

Jewell ML. Regulation of Ca2+ channels and exocytosis by receptors for prostaglandin E2. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1803/13495.

Council of Science Editors:

Jewell ML. Regulation of Ca2+ channels and exocytosis by receptors for prostaglandin E2. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://hdl.handle.net/1803/13495


Anna University

7. Nagarathnam, B. Genome wide survey of certain mammalian gpcrs and olfactory receptors; -.

Degree: Biotechnology, 2012, Anna University

In the recent era of Gprotein coupled receptor GPCR research newlinecomputational approaches in sequence analysis play a vital role in identifying newlinerelated sequences homologues conserved… (more)

Subjects/Keywords: Genome; Mammalian Gpcrs; Olfactory; orthologs; Receptors

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APA (6th Edition):

Nagarathnam, B. (2012). Genome wide survey of certain mammalian gpcrs and olfactory receptors; -. (Thesis). Anna University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/25889

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):

Nagarathnam, B. “Genome wide survey of certain mammalian gpcrs and olfactory receptors; -.” 2012. Thesis, Anna University. Accessed April 13, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/25889.

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

MLA Handbook (7th Edition):

Nagarathnam, B. “Genome wide survey of certain mammalian gpcrs and olfactory receptors; -.” 2012. Web. 13 Apr 2021.

Vancouver:

Nagarathnam B. Genome wide survey of certain mammalian gpcrs and olfactory receptors; -. [Internet] [Thesis]. Anna University; 2012. [cited 2021 Apr 13]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/25889.

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

Council of Science Editors:

Nagarathnam B. Genome wide survey of certain mammalian gpcrs and olfactory receptors; -. [Thesis]. Anna University; 2012. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/25889

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


University of Toronto

8. Pavlovic, Tea. Teneurin C-terminal Associated Peptide (TCAP)-1 Mediates Gonadotropin Releasing Hormone (GnRH) - independent Testosterone Production in Male Mice: Evidence from In vivo and In vitro Models.

Degree: 2016, University of Toronto

The teneurin C-terminal associated peptide (TCAP) is encoded by the terminal exon of each of the four teneurin genes, the established endogenous ligands of the… (more)

Subjects/Keywords: GPCRs; Neuroendocrinology; Peptides; Reproduction; Steroidogenesis; Testes; 0317

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APA (6th Edition):

Pavlovic, T. (2016). Teneurin C-terminal Associated Peptide (TCAP)-1 Mediates Gonadotropin Releasing Hormone (GnRH) - independent Testosterone Production in Male Mice: Evidence from In vivo and In vitro Models. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/75677

Chicago Manual of Style (16th Edition):

Pavlovic, Tea. “Teneurin C-terminal Associated Peptide (TCAP)-1 Mediates Gonadotropin Releasing Hormone (GnRH) - independent Testosterone Production in Male Mice: Evidence from In vivo and In vitro Models.” 2016. Masters Thesis, University of Toronto. Accessed April 13, 2021. http://hdl.handle.net/1807/75677.

MLA Handbook (7th Edition):

Pavlovic, Tea. “Teneurin C-terminal Associated Peptide (TCAP)-1 Mediates Gonadotropin Releasing Hormone (GnRH) - independent Testosterone Production in Male Mice: Evidence from In vivo and In vitro Models.” 2016. Web. 13 Apr 2021.

Vancouver:

Pavlovic T. Teneurin C-terminal Associated Peptide (TCAP)-1 Mediates Gonadotropin Releasing Hormone (GnRH) - independent Testosterone Production in Male Mice: Evidence from In vivo and In vitro Models. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1807/75677.

Council of Science Editors:

Pavlovic T. Teneurin C-terminal Associated Peptide (TCAP)-1 Mediates Gonadotropin Releasing Hormone (GnRH) - independent Testosterone Production in Male Mice: Evidence from In vivo and In vitro Models. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/75677


University of Toronto

9. Pavlovic, Tea. Teneurin C-terminal Associated Peptide (TCAP)-1 Mediates Gonadotropin Releasing Hormone (GnRH)–independent Testosterone Production in Male Mice: Evidence from In vivo and In vitro Models.

Degree: 2016, University of Toronto

The teneurin C-terminal associated peptide (TCAP) is encoded by the terminal exon of each of the four teneurin genes, the established endogenous ligands of the… (more)

Subjects/Keywords: GPCRs; Neuroendocrinology; Peptides; Reproduction; Steroidogenesis; Testes; 0317

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APA (6th Edition):

Pavlovic, T. (2016). Teneurin C-terminal Associated Peptide (TCAP)-1 Mediates Gonadotropin Releasing Hormone (GnRH)–independent Testosterone Production in Male Mice: Evidence from In vivo and In vitro Models. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/94469

Chicago Manual of Style (16th Edition):

Pavlovic, Tea. “Teneurin C-terminal Associated Peptide (TCAP)-1 Mediates Gonadotropin Releasing Hormone (GnRH)–independent Testosterone Production in Male Mice: Evidence from In vivo and In vitro Models.” 2016. Masters Thesis, University of Toronto. Accessed April 13, 2021. http://hdl.handle.net/1807/94469.

MLA Handbook (7th Edition):

Pavlovic, Tea. “Teneurin C-terminal Associated Peptide (TCAP)-1 Mediates Gonadotropin Releasing Hormone (GnRH)–independent Testosterone Production in Male Mice: Evidence from In vivo and In vitro Models.” 2016. Web. 13 Apr 2021.

Vancouver:

Pavlovic T. Teneurin C-terminal Associated Peptide (TCAP)-1 Mediates Gonadotropin Releasing Hormone (GnRH)–independent Testosterone Production in Male Mice: Evidence from In vivo and In vitro Models. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1807/94469.

Council of Science Editors:

Pavlovic T. Teneurin C-terminal Associated Peptide (TCAP)-1 Mediates Gonadotropin Releasing Hormone (GnRH)–independent Testosterone Production in Male Mice: Evidence from In vivo and In vitro Models. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/94469

10. Upadhyaya, Jasbir. Characterization of T2Rs in the vasculature and elucidation of T2R4 desensitization mechanism.

Degree: Oral Biology, 2014, University of Manitoba

 Humans can taste many compounds but are able to distinguish between five basic tastes, bitter, sweet, umami, sour and salt. Bitter taste, which is mediated… (more)

Subjects/Keywords: GPCRs; Desensitization

…5 1.4.1 Taste GPCRs – Bitter and Sweet/Umami receptors 8 1.5.1 Bitter taste signaling… …subunit GPCRs G protein-coupled receptors GRKs G protein-coupled receptor kinases GRK-KD G… …initiated by the interaction of taste molecules with G protein-coupled receptors (GPCRs)… …x29;. 1.4 Taste GPCRs The two best-characterized families of taste receptors, sweet/umami… …taste receptors: T1Rs Sweet and umami tastes are mediated by a family of three GPCRs, T1R1… 

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APA (6th Edition):

Upadhyaya, J. (2014). Characterization of T2Rs in the vasculature and elucidation of T2R4 desensitization mechanism. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/30604

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):

Upadhyaya, Jasbir. “Characterization of T2Rs in the vasculature and elucidation of T2R4 desensitization mechanism.” 2014. Thesis, University of Manitoba. Accessed April 13, 2021. http://hdl.handle.net/1993/30604.

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

MLA Handbook (7th Edition):

Upadhyaya, Jasbir. “Characterization of T2Rs in the vasculature and elucidation of T2R4 desensitization mechanism.” 2014. Web. 13 Apr 2021.

Vancouver:

Upadhyaya J. Characterization of T2Rs in the vasculature and elucidation of T2R4 desensitization mechanism. [Internet] [Thesis]. University of Manitoba; 2014. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1993/30604.

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

Council of Science Editors:

Upadhyaya J. Characterization of T2Rs in the vasculature and elucidation of T2R4 desensitization mechanism. [Thesis]. University of Manitoba; 2014. Available from: http://hdl.handle.net/1993/30604

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


Georgia Tech

11. Peterson, Vincent. Progress towards the development of G-protein coupled receptor based logic gates.

Degree: MS, Chemistry and Biochemistry, 2016, Georgia Tech

 The yeast Saccharomyces cerevisiae along with the bacterium Escherichia coli have been popular model organisms for the creation or modification of chemical producing or chemical… (more)

Subjects/Keywords: Synthetic biology; GPCRs; Yeast; Cell signaling; Biosensors

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APA (6th Edition):

Peterson, V. (2016). Progress towards the development of G-protein coupled receptor based logic gates. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58141

Chicago Manual of Style (16th Edition):

Peterson, Vincent. “Progress towards the development of G-protein coupled receptor based logic gates.” 2016. Masters Thesis, Georgia Tech. Accessed April 13, 2021. http://hdl.handle.net/1853/58141.

MLA Handbook (7th Edition):

Peterson, Vincent. “Progress towards the development of G-protein coupled receptor based logic gates.” 2016. Web. 13 Apr 2021.

Vancouver:

Peterson V. Progress towards the development of G-protein coupled receptor based logic gates. [Internet] [Masters thesis]. Georgia Tech; 2016. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1853/58141.

Council of Science Editors:

Peterson V. Progress towards the development of G-protein coupled receptor based logic gates. [Masters Thesis]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/58141

12. Gepoliano dos Santos Chaves. Investigação de PfSR25, putativo receptor serpentino de Plasmodium falciparum.

Degree: 2014, University of São Paulo

Este trabalho teve por objetivo dissecar o papel potencial de fosforilação/desfosforilação como efeitos da ativação de PfSR25, um candidato a receptor serpentina de P. falciparum.… (more)

Subjects/Keywords: Plasmodium falciparum; Cálcio; Fosfatases; GPCRs; Potássio; Quinases; Plasmodium falciparum; Calcium; GPCRs; Kinases; Phosphatases; Potassium

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APA (6th Edition):

Chaves, G. d. S. (2014). Investigação de PfSR25, putativo receptor serpentino de Plasmodium falciparum. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/42/42135/tde-28112014-135917/

Chicago Manual of Style (16th Edition):

Chaves, Gepoliano dos Santos. “Investigação de PfSR25, putativo receptor serpentino de Plasmodium falciparum.” 2014. Masters Thesis, University of São Paulo. Accessed April 13, 2021. http://www.teses.usp.br/teses/disponiveis/42/42135/tde-28112014-135917/.

MLA Handbook (7th Edition):

Chaves, Gepoliano dos Santos. “Investigação de PfSR25, putativo receptor serpentino de Plasmodium falciparum.” 2014. Web. 13 Apr 2021.

Vancouver:

Chaves GdS. Investigação de PfSR25, putativo receptor serpentino de Plasmodium falciparum. [Internet] [Masters thesis]. University of São Paulo; 2014. [cited 2021 Apr 13]. Available from: http://www.teses.usp.br/teses/disponiveis/42/42135/tde-28112014-135917/.

Council of Science Editors:

Chaves GdS. Investigação de PfSR25, putativo receptor serpentino de Plasmodium falciparum. [Masters Thesis]. University of São Paulo; 2014. Available from: http://www.teses.usp.br/teses/disponiveis/42/42135/tde-28112014-135917/

13. Alvaro, Christopher. Regulation of Saccharomyces cerevisiae Mating Pheromone Response: G-protein-coupled Receptor Ste2 Down-modulation by Specific α-Arrestins.

Degree: Molecular & Cell Biology, 2015, University of California – Berkeley

 The yeast G-protein-coupled receptor (GPCR) Ste2 is an integral plasma membrane protein that initiates response to an extracellular stimulus (the peptide mating pheromone α-factor) by… (more)

Subjects/Keywords: Molecular biology; Genetics; Biochemistry; arrestins; desensitization; GPCRs; internalization; S. cerevisiae

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APA (6th Edition):

Alvaro, C. (2015). Regulation of Saccharomyces cerevisiae Mating Pheromone Response: G-protein-coupled Receptor Ste2 Down-modulation by Specific α-Arrestins. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/1d678463

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):

Alvaro, Christopher. “Regulation of Saccharomyces cerevisiae Mating Pheromone Response: G-protein-coupled Receptor Ste2 Down-modulation by Specific α-Arrestins.” 2015. Thesis, University of California – Berkeley. Accessed April 13, 2021. http://www.escholarship.org/uc/item/1d678463.

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

MLA Handbook (7th Edition):

Alvaro, Christopher. “Regulation of Saccharomyces cerevisiae Mating Pheromone Response: G-protein-coupled Receptor Ste2 Down-modulation by Specific α-Arrestins.” 2015. Web. 13 Apr 2021.

Vancouver:

Alvaro C. Regulation of Saccharomyces cerevisiae Mating Pheromone Response: G-protein-coupled Receptor Ste2 Down-modulation by Specific α-Arrestins. [Internet] [Thesis]. University of California – Berkeley; 2015. [cited 2021 Apr 13]. Available from: http://www.escholarship.org/uc/item/1d678463.

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

Council of Science Editors:

Alvaro C. Regulation of Saccharomyces cerevisiae Mating Pheromone Response: G-protein-coupled Receptor Ste2 Down-modulation by Specific α-Arrestins. [Thesis]. University of California – Berkeley; 2015. Available from: http://www.escholarship.org/uc/item/1d678463

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

14. Papaoiconomou, Eleni. Παθοφυσιολογία του καρκίνου του μαστού: ο ρόλος της Kisspeptin.

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

BACKGROUND:Numerous studies have shown that the Kiss-1 gene countervails the metastatic aptitude of several cancer cell lines and solid-tumor neoplasias. However, there still remains ambiguity… (more)

Subjects/Keywords: Καρκίνος μαστού; AXOR12; GPCRs; GPR54; KISS-1; Breast cancer

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APA (6th Edition):

Papaoiconomou, E. (2014). Παθοφυσιολογία του καρκίνου του μαστού: ο ρόλος της Kisspeptin. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/42474

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):

Papaoiconomou, Eleni. “Παθοφυσιολογία του καρκίνου του μαστού: ο ρόλος της Kisspeptin.” 2014. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed April 13, 2021. http://hdl.handle.net/10442/hedi/42474.

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

MLA Handbook (7th Edition):

Papaoiconomou, Eleni. “Παθοφυσιολογία του καρκίνου του μαστού: ο ρόλος της Kisspeptin.” 2014. Web. 13 Apr 2021.

Vancouver:

Papaoiconomou E. Παθοφυσιολογία του καρκίνου του μαστού: ο ρόλος της Kisspeptin. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10442/hedi/42474.

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

Council of Science Editors:

Papaoiconomou E. Παθοφυσιολογία του καρκίνου του μαστού: ο ρόλος της Kisspeptin. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. Available from: http://hdl.handle.net/10442/hedi/42474

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


University of California – San Francisco

15. Eichel, Kelsie. Catalytic activation of beta-arrestins allows novel trafficking and signaling functions.

Degree: Biochemistry and Molecular Biology, 2017, University of California – San Francisco

 This thesis examines the trafficking and signaling functions of beta-arrestins, a highly conserved class of proteins that are critical regulators of G protein coupled receptor… (more)

Subjects/Keywords: Biology; arrestin; cell signaling; clathrin-coated pits; GPCRs; membrane trafficking; microscopy

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APA (6th Edition):

Eichel, K. (2017). Catalytic activation of beta-arrestins allows novel trafficking and signaling functions. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/1dw9s1x7

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):

Eichel, Kelsie. “Catalytic activation of beta-arrestins allows novel trafficking and signaling functions.” 2017. Thesis, University of California – San Francisco. Accessed April 13, 2021. http://www.escholarship.org/uc/item/1dw9s1x7.

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

MLA Handbook (7th Edition):

Eichel, Kelsie. “Catalytic activation of beta-arrestins allows novel trafficking and signaling functions.” 2017. Web. 13 Apr 2021.

Vancouver:

Eichel K. Catalytic activation of beta-arrestins allows novel trafficking and signaling functions. [Internet] [Thesis]. University of California – San Francisco; 2017. [cited 2021 Apr 13]. Available from: http://www.escholarship.org/uc/item/1dw9s1x7.

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

Council of Science Editors:

Eichel K. Catalytic activation of beta-arrestins allows novel trafficking and signaling functions. [Thesis]. University of California – San Francisco; 2017. Available from: http://www.escholarship.org/uc/item/1dw9s1x7

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


University of Manitoba

16. Pydi, Sai Prasad. Structural and functional characterization of bitter taste receptors, T2R1 and T2R4.

Degree: Oral Biology, 2011, University of Manitoba

 In humans, taste is one of the five senses, and helps in the recognition of nutritionally important and potentially harmful substances. It triggers innate behaviour… (more)

Subjects/Keywords: Bitter taste receptors; GPCRs; Taste; Bitter blockers; Over expression; Constitutive activity

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APA (6th Edition):

Pydi, S. P. (2011). Structural and functional characterization of bitter taste receptors, T2R1 and T2R4. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/23607

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):

Pydi, Sai Prasad. “Structural and functional characterization of bitter taste receptors, T2R1 and T2R4.” 2011. Thesis, University of Manitoba. Accessed April 13, 2021. http://hdl.handle.net/1993/23607.

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

MLA Handbook (7th Edition):

Pydi, Sai Prasad. “Structural and functional characterization of bitter taste receptors, T2R1 and T2R4.” 2011. Web. 13 Apr 2021.

Vancouver:

Pydi SP. Structural and functional characterization of bitter taste receptors, T2R1 and T2R4. [Internet] [Thesis]. University of Manitoba; 2011. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1993/23607.

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

Council of Science Editors:

Pydi SP. Structural and functional characterization of bitter taste receptors, T2R1 and T2R4. [Thesis]. University of Manitoba; 2011. Available from: http://hdl.handle.net/1993/23607

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


University of Arizona

17. Perera, Mahakumarage Suchithranga. Investigation of Rhodopsin Activation Using Spectroscopic and Scattering Techniques .

Degree: 2016, University of Arizona

 G-protein–coupled receptors are the largest superfamily in the human genome, and involved in critical cellular signaling processes in living cells. Protein structural fluctuations are the… (more)

Subjects/Keywords: Hydration; Membrane Proteins; Neutron Scattering; Protein Dynamics; Rhodopsin; GPCRs

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APA (6th Edition):

Perera, M. S. (2016). Investigation of Rhodopsin Activation Using Spectroscopic and Scattering Techniques . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/622975

Chicago Manual of Style (16th Edition):

Perera, Mahakumarage Suchithranga. “Investigation of Rhodopsin Activation Using Spectroscopic and Scattering Techniques .” 2016. Doctoral Dissertation, University of Arizona. Accessed April 13, 2021. http://hdl.handle.net/10150/622975.

MLA Handbook (7th Edition):

Perera, Mahakumarage Suchithranga. “Investigation of Rhodopsin Activation Using Spectroscopic and Scattering Techniques .” 2016. Web. 13 Apr 2021.

Vancouver:

Perera MS. Investigation of Rhodopsin Activation Using Spectroscopic and Scattering Techniques . [Internet] [Doctoral dissertation]. University of Arizona; 2016. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10150/622975.

Council of Science Editors:

Perera MS. Investigation of Rhodopsin Activation Using Spectroscopic and Scattering Techniques . [Doctoral Dissertation]. University of Arizona; 2016. Available from: http://hdl.handle.net/10150/622975

18. Kim, Donghun. Molecular physiology of tick salivary secretion and transcriptomics of tick in interaction with tick-borne pathogen.

Degree: PhD, Entomology, 2016, Kansas State University

 Tick salivary secretion is crucial for survival and for successful feeding. Tick saliva includes excretory water/ions and bioactive components for compromising the hosts' immune responses,… (more)

Subjects/Keywords: Na/K-ATPase; GPCRs; Salivary glands; Transcriptomics; Dopamine receptor

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APA (6th Edition):

Kim, D. (2016). Molecular physiology of tick salivary secretion and transcriptomics of tick in interaction with tick-borne pathogen. (Doctoral Dissertation). Kansas State University. Retrieved from http://hdl.handle.net/2097/32691

Chicago Manual of Style (16th Edition):

Kim, Donghun. “Molecular physiology of tick salivary secretion and transcriptomics of tick in interaction with tick-borne pathogen.” 2016. Doctoral Dissertation, Kansas State University. Accessed April 13, 2021. http://hdl.handle.net/2097/32691.

MLA Handbook (7th Edition):

Kim, Donghun. “Molecular physiology of tick salivary secretion and transcriptomics of tick in interaction with tick-borne pathogen.” 2016. Web. 13 Apr 2021.

Vancouver:

Kim D. Molecular physiology of tick salivary secretion and transcriptomics of tick in interaction with tick-borne pathogen. [Internet] [Doctoral dissertation]. Kansas State University; 2016. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2097/32691.

Council of Science Editors:

Kim D. Molecular physiology of tick salivary secretion and transcriptomics of tick in interaction with tick-borne pathogen. [Doctoral Dissertation]. Kansas State University; 2016. Available from: http://hdl.handle.net/2097/32691

19. Costa, Carina Alexandra Vaz da. Estudo comparativo e caracterização de novos elementos na regulação da homeostasia da glicose em teleósteos.

Degree: 2014, RCAAP

Dissertação de mestrado, Biotecnologia, Faculdade de Ciências e Tecnologia, Universidade do Algarve, 2014

A glicose é uma fonte importante de energia. Em mamíferos, o equilíbrio… (more)

Subjects/Keywords: Glicose; Glucagon; GPCRs; Peixes; Evolução; Função; Domínio/Área Científica::Ciências Naturais::Ciências Biológicas

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APA (6th Edition):

Costa, C. A. V. d. (2014). Estudo comparativo e caracterização de novos elementos na regulação da homeostasia da glicose em teleósteos. (Thesis). RCAAP. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:sapientia.ualg.pt:10400.1/8340

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):

Costa, Carina Alexandra Vaz da. “Estudo comparativo e caracterização de novos elementos na regulação da homeostasia da glicose em teleósteos.” 2014. Thesis, RCAAP. Accessed April 13, 2021. http://www.rcaap.pt/detail.jsp?id=oai:sapientia.ualg.pt:10400.1/8340.

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

MLA Handbook (7th Edition):

Costa, Carina Alexandra Vaz da. “Estudo comparativo e caracterização de novos elementos na regulação da homeostasia da glicose em teleósteos.” 2014. Web. 13 Apr 2021.

Vancouver:

Costa CAVd. Estudo comparativo e caracterização de novos elementos na regulação da homeostasia da glicose em teleósteos. [Internet] [Thesis]. RCAAP; 2014. [cited 2021 Apr 13]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:sapientia.ualg.pt:10400.1/8340.

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

Council of Science Editors:

Costa CAVd. Estudo comparativo e caracterização de novos elementos na regulação da homeostasia da glicose em teleósteos. [Thesis]. RCAAP; 2014. Available from: http://www.rcaap.pt/detail.jsp?id=oai:sapientia.ualg.pt:10400.1/8340

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

20. Rios Azuara, Santiago. Sequence and structure-based bioinformatic tools to the characterization, clustering and modeling of G-protein-coupled receptors (GPCRs).

Degree: Departament de Bioquímica i Biologia Molecular, 2017, Universitat Autònoma de Barcelona

 In this work, we developed new bioinformatic tools for the study of G-protein-coupled receptors (GPCRs). The pharmacological importance of these receptors motivates the development of… (more)

Subjects/Keywords: GPCRs; Anàlisi de seqüències; Análisis de secuencias; Sequence analysis; Bioinformàtica; Bioinformática; Bioinformatics; Ciències Experimentals; 577

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APA (6th Edition):

Rios Azuara, S. (2017). Sequence and structure-based bioinformatic tools to the characterization, clustering and modeling of G-protein-coupled receptors (GPCRs). (Thesis). Universitat Autònoma de Barcelona. Retrieved from http://hdl.handle.net/10803/457564

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):

Rios Azuara, Santiago. “Sequence and structure-based bioinformatic tools to the characterization, clustering and modeling of G-protein-coupled receptors (GPCRs).” 2017. Thesis, Universitat Autònoma de Barcelona. Accessed April 13, 2021. http://hdl.handle.net/10803/457564.

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

MLA Handbook (7th Edition):

Rios Azuara, Santiago. “Sequence and structure-based bioinformatic tools to the characterization, clustering and modeling of G-protein-coupled receptors (GPCRs).” 2017. Web. 13 Apr 2021.

Vancouver:

Rios Azuara S. Sequence and structure-based bioinformatic tools to the characterization, clustering and modeling of G-protein-coupled receptors (GPCRs). [Internet] [Thesis]. Universitat Autònoma de Barcelona; 2017. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10803/457564.

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

Council of Science Editors:

Rios Azuara S. Sequence and structure-based bioinformatic tools to the characterization, clustering and modeling of G-protein-coupled receptors (GPCRs). [Thesis]. Universitat Autònoma de Barcelona; 2017. Available from: http://hdl.handle.net/10803/457564

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


University of Melbourne

21. Vaid, Tasneem Murtuza. Determination of ligand binding conformations at α1-adrenergic receptor subtypes based on NMR and MD studies.

Degree: 2019, University of Melbourne

 Adrenergic receptor (AR) subtypes (α1A, α1B, α1D, α2A, α2B, α2C, β1, β2, β3) are G-protein coupled receptors (GPCRs) activated by the same endogenous catecholamines, adrenaline… (more)

Subjects/Keywords: GPCRs; adrenoceptors; adrenergic receptors; NMR; ligand-based NMR methods; molecular dynamics simulations

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APA (6th Edition):

Vaid, T. M. (2019). Determination of ligand binding conformations at α1-adrenergic receptor subtypes based on NMR and MD studies. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/227595

Chicago Manual of Style (16th Edition):

Vaid, Tasneem Murtuza. “Determination of ligand binding conformations at α1-adrenergic receptor subtypes based on NMR and MD studies.” 2019. Doctoral Dissertation, University of Melbourne. Accessed April 13, 2021. http://hdl.handle.net/11343/227595.

MLA Handbook (7th Edition):

Vaid, Tasneem Murtuza. “Determination of ligand binding conformations at α1-adrenergic receptor subtypes based on NMR and MD studies.” 2019. Web. 13 Apr 2021.

Vancouver:

Vaid TM. Determination of ligand binding conformations at α1-adrenergic receptor subtypes based on NMR and MD studies. [Internet] [Doctoral dissertation]. University of Melbourne; 2019. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/11343/227595.

Council of Science Editors:

Vaid TM. Determination of ligand binding conformations at α1-adrenergic receptor subtypes based on NMR and MD studies. [Doctoral Dissertation]. University of Melbourne; 2019. Available from: http://hdl.handle.net/11343/227595


Washington University in St. Louis

22. Harty, Breanne Leigh. Genetic and genomic dissections of myelinating glial cell development.

Degree: PhD, Biology & Biomedical Sciences (Developmental, Regenerative, & Stem Cell Biology), 2017, Washington University in St. Louis

 Myelin is a multilamellar sheath made by specialized glial cells that iteratively spiral and compact their plasma membranes around axon segments. In vertebrate nervous systems,… (more)

Subjects/Keywords: Adhesion GPCRs, Fbxw7, Genomics, Myelin, Schwann cells, Zebrafish; Developmental Biology; Genetics; Neuroscience and Neurobiology

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APA (6th Edition):

Harty, B. L. (2017). Genetic and genomic dissections of myelinating glial cell development. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/art_sci_etds/1109

Chicago Manual of Style (16th Edition):

Harty, Breanne Leigh. “Genetic and genomic dissections of myelinating glial cell development.” 2017. Doctoral Dissertation, Washington University in St. Louis. Accessed April 13, 2021. https://openscholarship.wustl.edu/art_sci_etds/1109.

MLA Handbook (7th Edition):

Harty, Breanne Leigh. “Genetic and genomic dissections of myelinating glial cell development.” 2017. Web. 13 Apr 2021.

Vancouver:

Harty BL. Genetic and genomic dissections of myelinating glial cell development. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2017. [cited 2021 Apr 13]. Available from: https://openscholarship.wustl.edu/art_sci_etds/1109.

Council of Science Editors:

Harty BL. Genetic and genomic dissections of myelinating glial cell development. [Doctoral Dissertation]. Washington University in St. Louis; 2017. Available from: https://openscholarship.wustl.edu/art_sci_etds/1109


University of Michigan

23. Denies, Maxwell. Investigation of How Receptor Localization and Endocytosis Regulate CXCR4 Signaling and Post-Translational Modification.

Degree: PhD, Cellular & Molecular Biology, 2020, University of Michigan

 Due to their great specificity and regulatory role in nearly all cellular processes, G protein-coupled receptors (GPCR) are a common therapeutic target. Investigating the molecular… (more)

Subjects/Keywords: GPCRs; CXCR4; Spatiotemporal Signaling; Endocytosis; GPCR post-translational modification; Molecular, Cellular and Developmental Biology; Science

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APA (6th Edition):

Denies, M. (2020). Investigation of How Receptor Localization and Endocytosis Regulate CXCR4 Signaling and Post-Translational Modification. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/163131

Chicago Manual of Style (16th Edition):

Denies, Maxwell. “Investigation of How Receptor Localization and Endocytosis Regulate CXCR4 Signaling and Post-Translational Modification.” 2020. Doctoral Dissertation, University of Michigan. Accessed April 13, 2021. http://hdl.handle.net/2027.42/163131.

MLA Handbook (7th Edition):

Denies, Maxwell. “Investigation of How Receptor Localization and Endocytosis Regulate CXCR4 Signaling and Post-Translational Modification.” 2020. Web. 13 Apr 2021.

Vancouver:

Denies M. Investigation of How Receptor Localization and Endocytosis Regulate CXCR4 Signaling and Post-Translational Modification. [Internet] [Doctoral dissertation]. University of Michigan; 2020. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2027.42/163131.

Council of Science Editors:

Denies M. Investigation of How Receptor Localization and Endocytosis Regulate CXCR4 Signaling and Post-Translational Modification. [Doctoral Dissertation]. University of Michigan; 2020. Available from: http://hdl.handle.net/2027.42/163131

24. Lima Neto, José Xavier de. Estudo em complexos fármaco-receptor utilizando bioquímica quântica.

Degree: 2019, Federal University of Rio Grande do Norte

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

O processo de desenho/desenvolvimento de fármacos vem tornando-se cada vez mais aperfeiçoado ao passo que outras… (more)

Subjects/Keywords: CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA; gpcrs; mfcc; Energia de interação; Serotonina; Gaba; Imunoterapia

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APA (6th Edition):

Lima Neto, J. X. d. (2019). Estudo em complexos fármaco-receptor utilizando bioquímica quântica. (Doctoral Dissertation). Federal University of Rio Grande do Norte. Retrieved from https://repositorio.ufrn.br/jspui/handle/123456789/26645

Chicago Manual of Style (16th Edition):

Lima Neto, José Xavier de. “Estudo em complexos fármaco-receptor utilizando bioquímica quântica.” 2019. Doctoral Dissertation, Federal University of Rio Grande do Norte. Accessed April 13, 2021. https://repositorio.ufrn.br/jspui/handle/123456789/26645.

MLA Handbook (7th Edition):

Lima Neto, José Xavier de. “Estudo em complexos fármaco-receptor utilizando bioquímica quântica.” 2019. Web. 13 Apr 2021.

Vancouver:

Lima Neto JXd. Estudo em complexos fármaco-receptor utilizando bioquímica quântica. [Internet] [Doctoral dissertation]. Federal University of Rio Grande do Norte; 2019. [cited 2021 Apr 13]. Available from: https://repositorio.ufrn.br/jspui/handle/123456789/26645.

Council of Science Editors:

Lima Neto JXd. Estudo em complexos fármaco-receptor utilizando bioquímica quântica. [Doctoral Dissertation]. Federal University of Rio Grande do Norte; 2019. Available from: https://repositorio.ufrn.br/jspui/handle/123456789/26645


Dalhousie University

25. 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 April 13, 2021. 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. 13 Apr 2021.

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 2021 Apr 13]. 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

26. Fedonides, Konstantinos. Μελέτη της έκφρασης γονιδίων που ρυθμίζουν την ενεργειακή ομοιόσταση στο κεντρικό νευρικό σύστημα σε μοντέλο παχυσαρκίας επίμυων.

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

The gut-brain axis maintains energy homeostasis through signaling of the membrane receptors for Growth Hormone Secretagogue (ghrelin)-GHSR, Leptin-LEPRb, Melanocortin-4 (a-MSH)-MC4R, and Cannabinoids-CB1R. The inter-regulation of… (more)

Subjects/Keywords: Παχυσαρκία; Επιμήκης γαστρεκτομή; Ενεργειακή ομοιόσταση; Υποδοχείς που συνδέονται με G-πρωτεΐνες; Υποθάλαμος; Obesity; Sleeve gastrectomy; Energy homeostasis; GPCRs; Hypothalamus

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APA (6th Edition):

Fedonides, K. (2014). Μελέτη της έκφρασης γονιδίων που ρυθμίζουν την ενεργειακή ομοιόσταση στο κεντρικό νευρικό σύστημα σε μοντέλο παχυσαρκίας επίμυων. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/40939

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):

Fedonides, Konstantinos. “Μελέτη της έκφρασης γονιδίων που ρυθμίζουν την ενεργειακή ομοιόσταση στο κεντρικό νευρικό σύστημα σε μοντέλο παχυσαρκίας επίμυων.” 2014. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed April 13, 2021. http://hdl.handle.net/10442/hedi/40939.

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

MLA Handbook (7th Edition):

Fedonides, Konstantinos. “Μελέτη της έκφρασης γονιδίων που ρυθμίζουν την ενεργειακή ομοιόσταση στο κεντρικό νευρικό σύστημα σε μοντέλο παχυσαρκίας επίμυων.” 2014. Web. 13 Apr 2021.

Vancouver:

Fedonides K. Μελέτη της έκφρασης γονιδίων που ρυθμίζουν την ενεργειακή ομοιόσταση στο κεντρικό νευρικό σύστημα σε μοντέλο παχυσαρκίας επίμυων. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10442/hedi/40939.

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

Council of Science Editors:

Fedonides K. Μελέτη της έκφρασης γονιδίων που ρυθμίζουν την ενεργειακή ομοιόσταση στο κεντρικό νευρικό σύστημα σε μοντέλο παχυσαρκίας επίμυων. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. Available from: http://hdl.handle.net/10442/hedi/40939

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


University of Waterloo

27. Gondora, Nyasha. GPCR and RTK Regulation in Neurons: The Impact of Stress on GPCR and RTK signalling and Crosstalk.

Degree: 2020, University of Waterloo

 Crosstalk between receptors allows for the integration of diverse and complex signalling pathways. Transactivation is a form of crosstalk between G-protein coupled receptors (GPCRs) and… (more)

Subjects/Keywords: G-protein coupled receptors (GPCRs); Receptor tyrosine Kinases (RTKs); TrkB; BDNF; NMDA; GluN2B; stress; Chronic early life social isolation (CELSI)

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APA (6th Edition):

Gondora, N. (2020). GPCR and RTK Regulation in Neurons: The Impact of Stress on GPCR and RTK signalling and Crosstalk. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/15751

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):

Gondora, Nyasha. “GPCR and RTK Regulation in Neurons: The Impact of Stress on GPCR and RTK signalling and Crosstalk.” 2020. Thesis, University of Waterloo. Accessed April 13, 2021. http://hdl.handle.net/10012/15751.

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

MLA Handbook (7th Edition):

Gondora, Nyasha. “GPCR and RTK Regulation in Neurons: The Impact of Stress on GPCR and RTK signalling and Crosstalk.” 2020. Web. 13 Apr 2021.

Vancouver:

Gondora N. GPCR and RTK Regulation in Neurons: The Impact of Stress on GPCR and RTK signalling and Crosstalk. [Internet] [Thesis]. University of Waterloo; 2020. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10012/15751.

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

Council of Science Editors:

Gondora N. GPCR and RTK Regulation in Neurons: The Impact of Stress on GPCR and RTK signalling and Crosstalk. [Thesis]. University of Waterloo; 2020. Available from: http://hdl.handle.net/10012/15751

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

28. Landomiel, Flavie. Propriétés signalétiques des B-arrestines : mise en évidence de nouveaux partenaires et implications fonctionnelles : Signaling properties of beta-arrestin : highlights on new partners and functional implications.

Degree: Docteur es, Santé, sciences biologiques et chimie du vivant, 2015, Université François-Rabelais de Tours

Les β-arrestines jouent un rôle important dans la transduction du signal par les récepteurs couplés aux protéines G (RCPG). Nous montrons dans cette thèse que… (more)

Subjects/Keywords: RCPGs; Β-arrestines; Voies de signalisation; R-FSH; V2R; GPCRs; Β-arrestins; Signaling pathways; R-FSH; V2R

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

APA (6th Edition):

Landomiel, F. (2015). Propriétés signalétiques des B-arrestines : mise en évidence de nouveaux partenaires et implications fonctionnelles : Signaling properties of beta-arrestin : highlights on new partners and functional implications. (Doctoral Dissertation). Université François-Rabelais de Tours. Retrieved from http://www.theses.fr/2015TOUR4044

Chicago Manual of Style (16th Edition):

Landomiel, Flavie. “Propriétés signalétiques des B-arrestines : mise en évidence de nouveaux partenaires et implications fonctionnelles : Signaling properties of beta-arrestin : highlights on new partners and functional implications.” 2015. Doctoral Dissertation, Université François-Rabelais de Tours. Accessed April 13, 2021. http://www.theses.fr/2015TOUR4044.

MLA Handbook (7th Edition):

Landomiel, Flavie. “Propriétés signalétiques des B-arrestines : mise en évidence de nouveaux partenaires et implications fonctionnelles : Signaling properties of beta-arrestin : highlights on new partners and functional implications.” 2015. Web. 13 Apr 2021.

Vancouver:

Landomiel F. Propriétés signalétiques des B-arrestines : mise en évidence de nouveaux partenaires et implications fonctionnelles : Signaling properties of beta-arrestin : highlights on new partners and functional implications. [Internet] [Doctoral dissertation]. Université François-Rabelais de Tours; 2015. [cited 2021 Apr 13]. Available from: http://www.theses.fr/2015TOUR4044.

Council of Science Editors:

Landomiel F. Propriétés signalétiques des B-arrestines : mise en évidence de nouveaux partenaires et implications fonctionnelles : Signaling properties of beta-arrestin : highlights on new partners and functional implications. [Doctoral Dissertation]. Université François-Rabelais de Tours; 2015. Available from: http://www.theses.fr/2015TOUR4044


Indian Institute of Science

29. Pal, Jagriti. Elucidating Deregulated Novel Pathways in Glioma through Genetic and Epigenetic Approaches.

Degree: PhD, Faculty of Science, 2019, Indian Institute of Science

 Malignancy of glial cells is termed as glioma. Gliomas comprise of thirty percent of all tumors of the central nervous system (CNS) and eighty percent… (more)

Subjects/Keywords: Glioma; Ependymoma; Oligodendroglioma; Astrocytoma; Glioblastoma; GBM Patients; G-protein Coupled Receptors (GPCRs); Microbiology and Cell Biology

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

APA (6th Edition):

Pal, J. (2019). Elucidating Deregulated Novel Pathways in Glioma through Genetic and Epigenetic Approaches. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/4284

Chicago Manual of Style (16th Edition):

Pal, Jagriti. “Elucidating Deregulated Novel Pathways in Glioma through Genetic and Epigenetic Approaches.” 2019. Doctoral Dissertation, Indian Institute of Science. Accessed April 13, 2021. http://etd.iisc.ac.in/handle/2005/4284.

MLA Handbook (7th Edition):

Pal, Jagriti. “Elucidating Deregulated Novel Pathways in Glioma through Genetic and Epigenetic Approaches.” 2019. Web. 13 Apr 2021.

Vancouver:

Pal J. Elucidating Deregulated Novel Pathways in Glioma through Genetic and Epigenetic Approaches. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2019. [cited 2021 Apr 13]. Available from: http://etd.iisc.ac.in/handle/2005/4284.

Council of Science Editors:

Pal J. Elucidating Deregulated Novel Pathways in Glioma through Genetic and Epigenetic Approaches. [Doctoral Dissertation]. Indian Institute of Science; 2019. Available from: http://etd.iisc.ac.in/handle/2005/4284

30. Esteoulle, Lucie. Développement de conjugués peptidiques fluorocarbonés pour augmenter la stabilité plasmatique de peptides visant des récepteurs couplés aux protéines G : Development of fluorocarbon peptide conjugates to increase the plasma stability of peptides targeting GPCRs.

Degree: Docteur es, Chimie, 2018, Université de Strasbourg

Afin d’améliorer la stabilité plasmatique de peptides, nous avons développé une nouvelle stratégie basée sur l’introduction d’une chaîne fluorocarbonée dans la séquence d’un peptide natif.… (more)

Subjects/Keywords: RCPG; Stabilité plasmatique; Chaîne fluorocarbonée; Thérapie; Peptides; GPCRs; Plasma stability; Fluorocarbon chain; Fluorescent probes; Therapy; 572.6

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

APA (6th Edition):

Esteoulle, L. (2018). Développement de conjugués peptidiques fluorocarbonés pour augmenter la stabilité plasmatique de peptides visant des récepteurs couplés aux protéines G : Development of fluorocarbon peptide conjugates to increase the plasma stability of peptides targeting GPCRs. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2018STRAF058

Chicago Manual of Style (16th Edition):

Esteoulle, Lucie. “Développement de conjugués peptidiques fluorocarbonés pour augmenter la stabilité plasmatique de peptides visant des récepteurs couplés aux protéines G : Development of fluorocarbon peptide conjugates to increase the plasma stability of peptides targeting GPCRs.” 2018. Doctoral Dissertation, Université de Strasbourg. Accessed April 13, 2021. http://www.theses.fr/2018STRAF058.

MLA Handbook (7th Edition):

Esteoulle, Lucie. “Développement de conjugués peptidiques fluorocarbonés pour augmenter la stabilité plasmatique de peptides visant des récepteurs couplés aux protéines G : Development of fluorocarbon peptide conjugates to increase the plasma stability of peptides targeting GPCRs.” 2018. Web. 13 Apr 2021.

Vancouver:

Esteoulle L. Développement de conjugués peptidiques fluorocarbonés pour augmenter la stabilité plasmatique de peptides visant des récepteurs couplés aux protéines G : Development of fluorocarbon peptide conjugates to increase the plasma stability of peptides targeting GPCRs. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2018. [cited 2021 Apr 13]. Available from: http://www.theses.fr/2018STRAF058.

Council of Science Editors:

Esteoulle L. Développement de conjugués peptidiques fluorocarbonés pour augmenter la stabilité plasmatique de peptides visant des récepteurs couplés aux protéines G : Development of fluorocarbon peptide conjugates to increase the plasma stability of peptides targeting GPCRs. [Doctoral Dissertation]. Université de Strasbourg; 2018. Available from: http://www.theses.fr/2018STRAF058

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