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You searched for subject:(GLP 1). Showing records 1 – 30 of 139 total matches.

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University of Toronto

1. Li, Samantha. Role of Vesicle-associated Membrane Protein 2 in Glucagon-like Peptide-1 Secretion.

Degree: 2013, University of Toronto

 Glucagon-like peptide-1 (GLP-1) is an incretin hormone produced by the enteroendocrine L-cell that potently stimulates insulin secretion. Although signaling pathways promoting GLP-1 secretion are well… (more)

Subjects/Keywords: GLP-1; VAMP2; SNARE

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

APA (6th Edition):

Li, S. (2013). Role of Vesicle-associated Membrane Protein 2 in Glucagon-like Peptide-1 Secretion. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/43079

Chicago Manual of Style (16th Edition):

Li, Samantha. “Role of Vesicle-associated Membrane Protein 2 in Glucagon-like Peptide-1 Secretion.” 2013. Masters Thesis, University of Toronto. Accessed October 23, 2019. http://hdl.handle.net/1807/43079.

MLA Handbook (7th Edition):

Li, Samantha. “Role of Vesicle-associated Membrane Protein 2 in Glucagon-like Peptide-1 Secretion.” 2013. Web. 23 Oct 2019.

Vancouver:

Li S. Role of Vesicle-associated Membrane Protein 2 in Glucagon-like Peptide-1 Secretion. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/1807/43079.

Council of Science Editors:

Li S. Role of Vesicle-associated Membrane Protein 2 in Glucagon-like Peptide-1 Secretion. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/43079


University of Toronto

2. Mulherin, Andrew. Mechanisms underlying Metformin-induced Secretion of Glucagon-like Peptide-1 from the Intestinal L-cell.

Degree: 2011, University of Toronto

The incretin hormone glucagon-like peptide-1 enhances glucose-dependent insulin secretion and is therefore a most attractive therapeutic approach for the treatment of Type 2 Diabetes Mellitus.… (more)

Subjects/Keywords: metformin; GLP-1; 0719

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APA (6th Edition):

Mulherin, A. (2011). Mechanisms underlying Metformin-induced Secretion of Glucagon-like Peptide-1 from the Intestinal L-cell. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/31353

Chicago Manual of Style (16th Edition):

Mulherin, Andrew. “Mechanisms underlying Metformin-induced Secretion of Glucagon-like Peptide-1 from the Intestinal L-cell.” 2011. Masters Thesis, University of Toronto. Accessed October 23, 2019. http://hdl.handle.net/1807/31353.

MLA Handbook (7th Edition):

Mulherin, Andrew. “Mechanisms underlying Metformin-induced Secretion of Glucagon-like Peptide-1 from the Intestinal L-cell.” 2011. Web. 23 Oct 2019.

Vancouver:

Mulherin A. Mechanisms underlying Metformin-induced Secretion of Glucagon-like Peptide-1 from the Intestinal L-cell. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/1807/31353.

Council of Science Editors:

Mulherin A. Mechanisms underlying Metformin-induced Secretion of Glucagon-like Peptide-1 from the Intestinal L-cell. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/31353


University of Cincinnati

3. Klustaitis, Kori M. Activation of the central nervous system by circulating Glucagon-Like Peptide-1.

Degree: PhD, Medicine : Pathobiology and Molecular Medicine, 2009, University of Cincinnati

  The aim of this dissertation research was to investigate how Glucagon-Like Peptide-1 activates the central nervous system to illicit changes in blood glucose. Understanding… (more)

Subjects/Keywords: Biology; GLP-1; GLP-1r; vagal; vagal afferents; afferent; Tracer; intestine

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APA (6th Edition):

Klustaitis, K. M. (2009). Activation of the central nervous system by circulating Glucagon-Like Peptide-1. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1243357633

Chicago Manual of Style (16th Edition):

Klustaitis, Kori M. “Activation of the central nervous system by circulating Glucagon-Like Peptide-1.” 2009. Doctoral Dissertation, University of Cincinnati. Accessed October 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1243357633.

MLA Handbook (7th Edition):

Klustaitis, Kori M. “Activation of the central nervous system by circulating Glucagon-Like Peptide-1.” 2009. Web. 23 Oct 2019.

Vancouver:

Klustaitis KM. Activation of the central nervous system by circulating Glucagon-Like Peptide-1. [Internet] [Doctoral dissertation]. University of Cincinnati; 2009. [cited 2019 Oct 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1243357633.

Council of Science Editors:

Klustaitis KM. Activation of the central nervous system by circulating Glucagon-Like Peptide-1. [Doctoral Dissertation]. University of Cincinnati; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1243357633


University of Cambridge

4. Biggs, Emma Kate. Generation and use of new tools for the characterisation of gut hormone receptors .

Degree: 2019, University of Cambridge

 Enteroendocrine hormones released from the intestine following food intake have several roles in the control of metabolism, some of which are exploited therapeutically for the… (more)

Subjects/Keywords: Enteroendocrine; Gut hormone receptors; GLP-1; GLP-2; GIP

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APA (6th Edition):

Biggs, E. K. (2019). Generation and use of new tools for the characterisation of gut hormone receptors . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/290259

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):

Biggs, Emma Kate. “Generation and use of new tools for the characterisation of gut hormone receptors .” 2019. Thesis, University of Cambridge. Accessed October 23, 2019. https://www.repository.cam.ac.uk/handle/1810/290259.

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

MLA Handbook (7th Edition):

Biggs, Emma Kate. “Generation and use of new tools for the characterisation of gut hormone receptors .” 2019. Web. 23 Oct 2019.

Vancouver:

Biggs EK. Generation and use of new tools for the characterisation of gut hormone receptors . [Internet] [Thesis]. University of Cambridge; 2019. [cited 2019 Oct 23]. Available from: https://www.repository.cam.ac.uk/handle/1810/290259.

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

Council of Science Editors:

Biggs EK. Generation and use of new tools for the characterisation of gut hormone receptors . [Thesis]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/290259

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


Texas A&M University

5. Gearing, Merrick Hume. The Effects of Emulsions on the Upregulation of Satiety Hormones in Cell Culture and the Activation of the Ileal Brake in Human Subjects.

Degree: 2015, Texas A&M University

 To treat obesity, one approach is developing food products formulated to trigger the ileal brake, a gastric feedback mechanism that induces satiety, the prolonged feeling… (more)

Subjects/Keywords: ileal brake; Peptide YY; GLP-1; satiety

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APA (6th Edition):

Gearing, M. H. (2015). The Effects of Emulsions on the Upregulation of Satiety Hormones in Cell Culture and the Activation of the Ileal Brake in Human Subjects. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/155405

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):

Gearing, Merrick Hume. “The Effects of Emulsions on the Upregulation of Satiety Hormones in Cell Culture and the Activation of the Ileal Brake in Human Subjects.” 2015. Thesis, Texas A&M University. Accessed October 23, 2019. http://hdl.handle.net/1969.1/155405.

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

MLA Handbook (7th Edition):

Gearing, Merrick Hume. “The Effects of Emulsions on the Upregulation of Satiety Hormones in Cell Culture and the Activation of the Ileal Brake in Human Subjects.” 2015. Web. 23 Oct 2019.

Vancouver:

Gearing MH. The Effects of Emulsions on the Upregulation of Satiety Hormones in Cell Culture and the Activation of the Ileal Brake in Human Subjects. [Internet] [Thesis]. Texas A&M University; 2015. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/1969.1/155405.

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

Council of Science Editors:

Gearing MH. The Effects of Emulsions on the Upregulation of Satiety Hormones in Cell Culture and the Activation of the Ileal Brake in Human Subjects. [Thesis]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/155405

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


University College Cork

6. Kent, Robert M. Microbially derived bioactive peptides to improve human health.

Degree: 2014, University College Cork

 This thesis describes a study of various methods to produce bioactive peptides. Initially, the generation of anti-Cronobacter spp. peptides by fermentation of milk protein is… (more)

Subjects/Keywords: Bioactive peptides; Antimicrobial; Cronobacter; GLP-1; Diabetes

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APA (6th Edition):

Kent, R. M. (2014). Microbially derived bioactive peptides to improve human health. (Thesis). University College Cork. Retrieved from http://hdl.handle.net/10468/3463

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):

Kent, Robert M. “Microbially derived bioactive peptides to improve human health.” 2014. Thesis, University College Cork. Accessed October 23, 2019. http://hdl.handle.net/10468/3463.

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

MLA Handbook (7th Edition):

Kent, Robert M. “Microbially derived bioactive peptides to improve human health.” 2014. Web. 23 Oct 2019.

Vancouver:

Kent RM. Microbially derived bioactive peptides to improve human health. [Internet] [Thesis]. University College Cork; 2014. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10468/3463.

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

Council of Science Editors:

Kent RM. Microbially derived bioactive peptides to improve human health. [Thesis]. University College Cork; 2014. Available from: http://hdl.handle.net/10468/3463

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

7. Maraver Selfa, Silvia María. Niveles de GLP-1 tras el test de sobrecarga oral de glucosa en mujeres con antecedentes de diabetes mellitus gestacional.

Degree: 2017, Servicio de Publicaciones y Divulgación Científica

 Se ha descrito una reducción significativa del efecto incretina en pacientes con DM2 que puede deberse a la secreción alterada de las hormonas incretinas y/o… (more)

Subjects/Keywords: Diabetes; GLP-1; Diabetes gestacional; Tesis Doctoral

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APA (6th Edition):

Maraver Selfa, S. M. (2017). Niveles de GLP-1 tras el test de sobrecarga oral de glucosa en mujeres con antecedentes de diabetes mellitus gestacional. (Thesis). Servicio de Publicaciones y Divulgación Científica. Retrieved from http://hdl.handle.net/10630/13059

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):

Maraver Selfa, Silvia María. “Niveles de GLP-1 tras el test de sobrecarga oral de glucosa en mujeres con antecedentes de diabetes mellitus gestacional.” 2017. Thesis, Servicio de Publicaciones y Divulgación Científica. Accessed October 23, 2019. http://hdl.handle.net/10630/13059.

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

MLA Handbook (7th Edition):

Maraver Selfa, Silvia María. “Niveles de GLP-1 tras el test de sobrecarga oral de glucosa en mujeres con antecedentes de diabetes mellitus gestacional.” 2017. Web. 23 Oct 2019.

Vancouver:

Maraver Selfa SM. Niveles de GLP-1 tras el test de sobrecarga oral de glucosa en mujeres con antecedentes de diabetes mellitus gestacional. [Internet] [Thesis]. Servicio de Publicaciones y Divulgación Científica; 2017. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10630/13059.

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

Council of Science Editors:

Maraver Selfa SM. Niveles de GLP-1 tras el test de sobrecarga oral de glucosa en mujeres con antecedentes de diabetes mellitus gestacional. [Thesis]. Servicio de Publicaciones y Divulgación Científica; 2017. Available from: http://hdl.handle.net/10630/13059

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


Boston University

8. Behbahani, Sara. The role of GLP-1 receptor agonist as a potential treatment for non-alcoholic fatty liver disease and non-alcoholic steatohepatitis.

Degree: MS, Medical Sciences, 2017, Boston University

 Non-alcoholic fatty liver disease (NAFLD) is the most common cause of liver dysfunction in the western world and one of the main contributors to cirrhosis… (more)

Subjects/Keywords: Medicine; GLP-1; NASH; Metabolic syndrome

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APA (6th Edition):

Behbahani, S. (2017). The role of GLP-1 receptor agonist as a potential treatment for non-alcoholic fatty liver disease and non-alcoholic steatohepatitis. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/26621

Chicago Manual of Style (16th Edition):

Behbahani, Sara. “The role of GLP-1 receptor agonist as a potential treatment for non-alcoholic fatty liver disease and non-alcoholic steatohepatitis.” 2017. Masters Thesis, Boston University. Accessed October 23, 2019. http://hdl.handle.net/2144/26621.

MLA Handbook (7th Edition):

Behbahani, Sara. “The role of GLP-1 receptor agonist as a potential treatment for non-alcoholic fatty liver disease and non-alcoholic steatohepatitis.” 2017. Web. 23 Oct 2019.

Vancouver:

Behbahani S. The role of GLP-1 receptor agonist as a potential treatment for non-alcoholic fatty liver disease and non-alcoholic steatohepatitis. [Internet] [Masters thesis]. Boston University; 2017. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/2144/26621.

Council of Science Editors:

Behbahani S. The role of GLP-1 receptor agonist as a potential treatment for non-alcoholic fatty liver disease and non-alcoholic steatohepatitis. [Masters Thesis]. Boston University; 2017. Available from: http://hdl.handle.net/2144/26621


Université Laval

9. Barbuta, Mihaela. Le rôle de la kinase activée par l'AMP dans l'effet insulinotropique du GLP-1.

Degree: 2011, Université Laval

 La sécrétion d'insuline stimulée par les incrétines tels le GLP-1 (glucagon-like peptide-1) et le GIP (glucose-dependent insulinotropic polypeptide), a un rôle majeur dans la régulation… (more)

Subjects/Keywords: Protéines kinases; AMP cyclique; GLP-1; Insuline

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APA (6th Edition):

Barbuta, M. (2011). Le rôle de la kinase activée par l'AMP dans l'effet insulinotropique du GLP-1. (Thesis). Université Laval. Retrieved from http://hdl.handle.net/20.500.11794/23156

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):

Barbuta, Mihaela. “Le rôle de la kinase activée par l'AMP dans l'effet insulinotropique du GLP-1.” 2011. Thesis, Université Laval. Accessed October 23, 2019. http://hdl.handle.net/20.500.11794/23156.

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

MLA Handbook (7th Edition):

Barbuta, Mihaela. “Le rôle de la kinase activée par l'AMP dans l'effet insulinotropique du GLP-1.” 2011. Web. 23 Oct 2019.

Vancouver:

Barbuta M. Le rôle de la kinase activée par l'AMP dans l'effet insulinotropique du GLP-1. [Internet] [Thesis]. Université Laval; 2011. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/20.500.11794/23156.

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

Council of Science Editors:

Barbuta M. Le rôle de la kinase activée par l'AMP dans l'effet insulinotropique du GLP-1. [Thesis]. Université Laval; 2011. Available from: http://hdl.handle.net/20.500.11794/23156

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


University of Manitoba

10. Fry, Mark. Electrophysiological characterization of catecholamine-containing GFP-expressing dissociated mouse area postrema neurons and their response to glucagon-like peptide-1 receptor agonists.

Degree: Biological Sciences, 2017, University of Manitoba

 The area postrema (AP) is a hindbrain sensory circumventricular organ that participates in energy balance regulation. Catecholamine-containing AP neurons are a key subpopulation that inhibit… (more)

Subjects/Keywords: Electrophysiology; GLP-1; Area postrema; Tyrosine hydroxylase

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APA (6th Edition):

Fry, M. (2017). Electrophysiological characterization of catecholamine-containing GFP-expressing dissociated mouse area postrema neurons and their response to glucagon-like peptide-1 receptor agonists. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/32494

Chicago Manual of Style (16th Edition):

Fry, Mark. “Electrophysiological characterization of catecholamine-containing GFP-expressing dissociated mouse area postrema neurons and their response to glucagon-like peptide-1 receptor agonists.” 2017. Masters Thesis, University of Manitoba. Accessed October 23, 2019. http://hdl.handle.net/1993/32494.

MLA Handbook (7th Edition):

Fry, Mark. “Electrophysiological characterization of catecholamine-containing GFP-expressing dissociated mouse area postrema neurons and their response to glucagon-like peptide-1 receptor agonists.” 2017. Web. 23 Oct 2019.

Vancouver:

Fry M. Electrophysiological characterization of catecholamine-containing GFP-expressing dissociated mouse area postrema neurons and their response to glucagon-like peptide-1 receptor agonists. [Internet] [Masters thesis]. University of Manitoba; 2017. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/1993/32494.

Council of Science Editors:

Fry M. Electrophysiological characterization of catecholamine-containing GFP-expressing dissociated mouse area postrema neurons and their response to glucagon-like peptide-1 receptor agonists. [Masters Thesis]. University of Manitoba; 2017. Available from: http://hdl.handle.net/1993/32494


University of Toronto

11. Huang, Xinyi. The Identification of Novel Proteins that Interact with the GLP-1 Receptor and Restrain its Activity.

Degree: 2013, University of Toronto

G-protein coupled receptors (GPCRs) have been shown to interact with an array of accessory proteins that modulate their function. I hypothesize that the GLP-1R, a… (more)

Subjects/Keywords: GLP-1 Receptor; Protein Interactions; 0410; 0379

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APA (6th Edition):

Huang, X. (2013). The Identification of Novel Proteins that Interact with the GLP-1 Receptor and Restrain its Activity. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/42870

Chicago Manual of Style (16th Edition):

Huang, Xinyi. “The Identification of Novel Proteins that Interact with the GLP-1 Receptor and Restrain its Activity.” 2013. Masters Thesis, University of Toronto. Accessed October 23, 2019. http://hdl.handle.net/1807/42870.

MLA Handbook (7th Edition):

Huang, Xinyi. “The Identification of Novel Proteins that Interact with the GLP-1 Receptor and Restrain its Activity.” 2013. Web. 23 Oct 2019.

Vancouver:

Huang X. The Identification of Novel Proteins that Interact with the GLP-1 Receptor and Restrain its Activity. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/1807/42870.

Council of Science Editors:

Huang X. The Identification of Novel Proteins that Interact with the GLP-1 Receptor and Restrain its Activity. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/42870

12. Mohamed, Mohamed Abdullahi. GLP-1 REGULATES PROLIFERATION OF GLP-1 SECRETING CELLS THROUGH A FEEDBACK MECHANISM.

Degree: Sustainable Development of Society and Technology, 2010, Mälardalen University

  Abstract <em> Background and aim: Diabetes mellitus (DM) is a chronic and progressive illness that affects all type of populations and ages. According to… (more)

Subjects/Keywords: Incretin hormone; GLP-1; GLP-1 receptor; Exendin-4; Diabetes; Endocrinology; Endokrinologi

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APA (6th Edition):

Mohamed, M. A. (2010). GLP-1 REGULATES PROLIFERATION OF GLP-1 SECRETING CELLS THROUGH A FEEDBACK MECHANISM. (Thesis). Mälardalen University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:mdh:diva-9756

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):

Mohamed, Mohamed Abdullahi. “GLP-1 REGULATES PROLIFERATION OF GLP-1 SECRETING CELLS THROUGH A FEEDBACK MECHANISM.” 2010. Thesis, Mälardalen University. Accessed October 23, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:mdh:diva-9756.

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

MLA Handbook (7th Edition):

Mohamed, Mohamed Abdullahi. “GLP-1 REGULATES PROLIFERATION OF GLP-1 SECRETING CELLS THROUGH A FEEDBACK MECHANISM.” 2010. Web. 23 Oct 2019.

Vancouver:

Mohamed MA. GLP-1 REGULATES PROLIFERATION OF GLP-1 SECRETING CELLS THROUGH A FEEDBACK MECHANISM. [Internet] [Thesis]. Mälardalen University; 2010. [cited 2019 Oct 23]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:mdh:diva-9756.

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

Council of Science Editors:

Mohamed MA. GLP-1 REGULATES PROLIFERATION OF GLP-1 SECRETING CELLS THROUGH A FEEDBACK MECHANISM. [Thesis]. Mälardalen University; 2010. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:mdh:diva-9756

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


University of Cambridge

13. Clarke, Sophie. The Cardiovascular Effect of GLP-1 in Humans .

Degree: 2019, University of Cambridge

 The incretin glucagon-like peptide-1 (GLP-1) abolishes post-ischemic left ventricular contractility (stunning) in humans but the mechanism remains elusive. I hypothesized that this effect is mediated… (more)

Subjects/Keywords: glucagon-like peptide-1; cardioprotection; GLP-1; coronary haemodynamics

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APA (6th Edition):

Clarke, S. (2019). The Cardiovascular Effect of GLP-1 in Humans . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/294378

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):

Clarke, Sophie. “The Cardiovascular Effect of GLP-1 in Humans .” 2019. Thesis, University of Cambridge. Accessed October 23, 2019. https://www.repository.cam.ac.uk/handle/1810/294378.

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

MLA Handbook (7th Edition):

Clarke, Sophie. “The Cardiovascular Effect of GLP-1 in Humans .” 2019. Web. 23 Oct 2019.

Vancouver:

Clarke S. The Cardiovascular Effect of GLP-1 in Humans . [Internet] [Thesis]. University of Cambridge; 2019. [cited 2019 Oct 23]. Available from: https://www.repository.cam.ac.uk/handle/1810/294378.

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

Council of Science Editors:

Clarke S. The Cardiovascular Effect of GLP-1 in Humans . [Thesis]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/294378

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


University of Cambridge

14. Clarke, Sophie. The cardiovascular effect of GLP-1 in humans.

Degree: PhD, 2019, University of Cambridge

 The incretin glucagon-like peptide-1 (GLP-1) abolishes post-ischemic left ventricular contractility (stunning) in humans but the mechanism remains elusive. I hypothesized that this effect is mediated… (more)

Subjects/Keywords: glucagon-like peptide-1; cardioprotection; GLP-1; coronary haemodynamics

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

APA (6th Edition):

Clarke, S. (2019). The cardiovascular effect of GLP-1 in humans. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/294378 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782790

Chicago Manual of Style (16th Edition):

Clarke, Sophie. “The cardiovascular effect of GLP-1 in humans.” 2019. Doctoral Dissertation, University of Cambridge. Accessed October 23, 2019. https://www.repository.cam.ac.uk/handle/1810/294378 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782790.

MLA Handbook (7th Edition):

Clarke, Sophie. “The cardiovascular effect of GLP-1 in humans.” 2019. Web. 23 Oct 2019.

Vancouver:

Clarke S. The cardiovascular effect of GLP-1 in humans. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2019 Oct 23]. Available from: https://www.repository.cam.ac.uk/handle/1810/294378 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782790.

Council of Science Editors:

Clarke S. The cardiovascular effect of GLP-1 in humans. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/294378 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782790

15. Ronveaux, Charlotte. Mécanisme des hormones anorexigènes régulant la prise alimentaire au niveau du nerf vague : Mechanisms of action of satiating gut peptides in the regulation of food intake through vagal afferent pathways.

Degree: Docteur es, Sciences de la vie et santé, 2015, Paris, AgroParisTech

Le tractus gastro-intestinal, interface initiale pour la détection, la digestion et l'absorption des nutriments, joue un rôle critique dans la régulation de l'homéostasie énergétique. Les… (more)

Subjects/Keywords: Glp-1; Leptine; Nerf vague; Prise alimentaire; Connexion intestin/cerveau; Glp-1; Leptin; Vagus nerve; Food intake; Gut-Brain Signaling; 612.391

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

APA (6th Edition):

Ronveaux, C. (2015). Mécanisme des hormones anorexigènes régulant la prise alimentaire au niveau du nerf vague : Mechanisms of action of satiating gut peptides in the regulation of food intake through vagal afferent pathways. (Doctoral Dissertation). Paris, AgroParisTech. Retrieved from http://www.theses.fr/2015AGPT0002

Chicago Manual of Style (16th Edition):

Ronveaux, Charlotte. “Mécanisme des hormones anorexigènes régulant la prise alimentaire au niveau du nerf vague : Mechanisms of action of satiating gut peptides in the regulation of food intake through vagal afferent pathways.” 2015. Doctoral Dissertation, Paris, AgroParisTech. Accessed October 23, 2019. http://www.theses.fr/2015AGPT0002.

MLA Handbook (7th Edition):

Ronveaux, Charlotte. “Mécanisme des hormones anorexigènes régulant la prise alimentaire au niveau du nerf vague : Mechanisms of action of satiating gut peptides in the regulation of food intake through vagal afferent pathways.” 2015. Web. 23 Oct 2019.

Vancouver:

Ronveaux C. Mécanisme des hormones anorexigènes régulant la prise alimentaire au niveau du nerf vague : Mechanisms of action of satiating gut peptides in the regulation of food intake through vagal afferent pathways. [Internet] [Doctoral dissertation]. Paris, AgroParisTech; 2015. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2015AGPT0002.

Council of Science Editors:

Ronveaux C. Mécanisme des hormones anorexigènes régulant la prise alimentaire au niveau du nerf vague : Mechanisms of action of satiating gut peptides in the regulation of food intake through vagal afferent pathways. [Doctoral Dissertation]. Paris, AgroParisTech; 2015. Available from: http://www.theses.fr/2015AGPT0002

16. Pappalardo, Alessandro Orazio Giovanni. Ruolo del recettore Gabaa nelle cellule alfa pancreatiche e suo coinvolgimento nelle fasi di desensibilizzazione indotta dalla lipotossicità nel diabete di tipo II.

Degree: 2016, Università degli Studi di Catania

 Il GABA o acido gamma-aminobutirrico è il principale neurotrasmettitore inibitorio del sistema nervoso centrale (SNC) dei mammiferi. Circa il 20 - 50% di tutte le… (more)

Subjects/Keywords: Area 06 - Scienze mediche; GABA, GLP-1, Lipotoxicity, Insulin Resistance, Glucagon, Incretin, GABA, GLP-1, Lipotossicità, Insulino Resistenza, Glicagone, Incretine

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

APA (6th Edition):

Pappalardo, A. O. G. (2016). Ruolo del recettore Gabaa nelle cellule alfa pancreatiche e suo coinvolgimento nelle fasi di desensibilizzazione indotta dalla lipotossicità nel diabete di tipo II. (Thesis). Università degli Studi di Catania. Retrieved from http://hdl.handle.net/10761/3991

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):

Pappalardo, Alessandro Orazio Giovanni. “Ruolo del recettore Gabaa nelle cellule alfa pancreatiche e suo coinvolgimento nelle fasi di desensibilizzazione indotta dalla lipotossicità nel diabete di tipo II.” 2016. Thesis, Università degli Studi di Catania. Accessed October 23, 2019. http://hdl.handle.net/10761/3991.

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

MLA Handbook (7th Edition):

Pappalardo, Alessandro Orazio Giovanni. “Ruolo del recettore Gabaa nelle cellule alfa pancreatiche e suo coinvolgimento nelle fasi di desensibilizzazione indotta dalla lipotossicità nel diabete di tipo II.” 2016. Web. 23 Oct 2019.

Vancouver:

Pappalardo AOG. Ruolo del recettore Gabaa nelle cellule alfa pancreatiche e suo coinvolgimento nelle fasi di desensibilizzazione indotta dalla lipotossicità nel diabete di tipo II. [Internet] [Thesis]. Università degli Studi di Catania; 2016. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10761/3991.

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

Council of Science Editors:

Pappalardo AOG. Ruolo del recettore Gabaa nelle cellule alfa pancreatiche e suo coinvolgimento nelle fasi di desensibilizzazione indotta dalla lipotossicità nel diabete di tipo II. [Thesis]. Università degli Studi di Catania; 2016. Available from: http://hdl.handle.net/10761/3991

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

17. Grasset, Estelle. Mécanismes moléculaires régulant l'action du glucagon-like peptide one dans la physiopathologie du diabète de type 2 : Molecular mechanisms regulating glucagon-like peptide one action in type 2 diabetes.

Degree: Docteur es, Maladies métaboliques et cardiovasculaires, 2016, Université Toulouse III – Paul Sabatier

Selon l'organisation mondiale de la santé, le diabète de type II (DT2), caractérisé par un défaut de contrôle de la glycémie, est une des causes… (more)

Subjects/Keywords: Glucagon-like peptide one (GLP-1); Diabètes; Récepteur au GLP-1; Microbiote intestinal; Neurones; Clock genes; Intestin

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

APA (6th Edition):

Grasset, E. (2016). Mécanismes moléculaires régulant l'action du glucagon-like peptide one dans la physiopathologie du diabète de type 2 : Molecular mechanisms regulating glucagon-like peptide one action in type 2 diabetes. (Doctoral Dissertation). Université Toulouse III – Paul Sabatier. Retrieved from http://www.theses.fr/2016TOU30301

Chicago Manual of Style (16th Edition):

Grasset, Estelle. “Mécanismes moléculaires régulant l'action du glucagon-like peptide one dans la physiopathologie du diabète de type 2 : Molecular mechanisms regulating glucagon-like peptide one action in type 2 diabetes.” 2016. Doctoral Dissertation, Université Toulouse III – Paul Sabatier. Accessed October 23, 2019. http://www.theses.fr/2016TOU30301.

MLA Handbook (7th Edition):

Grasset, Estelle. “Mécanismes moléculaires régulant l'action du glucagon-like peptide one dans la physiopathologie du diabète de type 2 : Molecular mechanisms regulating glucagon-like peptide one action in type 2 diabetes.” 2016. Web. 23 Oct 2019.

Vancouver:

Grasset E. Mécanismes moléculaires régulant l'action du glucagon-like peptide one dans la physiopathologie du diabète de type 2 : Molecular mechanisms regulating glucagon-like peptide one action in type 2 diabetes. [Internet] [Doctoral dissertation]. Université Toulouse III – Paul Sabatier; 2016. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2016TOU30301.

Council of Science Editors:

Grasset E. Mécanismes moléculaires régulant l'action du glucagon-like peptide one dans la physiopathologie du diabète de type 2 : Molecular mechanisms regulating glucagon-like peptide one action in type 2 diabetes. [Doctoral Dissertation]. Université Toulouse III – Paul Sabatier; 2016. Available from: http://www.theses.fr/2016TOU30301

18. Martin, Céline. Détection gustative des lipides alimentaires chez la souris : portrait croisé de deux lipido-récepteurs, CD36 & GPR120 : impacts sur les préférences alimentaires et la santé : Gustatory detection of dietary lipids in the mouse : crossed portrait of two lipid-sensors CD36 & GPR120 : impacts on food preferences and health.

Degree: Docteur es, Sciences de la vie, 2011, Université de Bourgogne

Certains mammifères, dont l’Homme, ont une forte attraction pour les lipides alimentaires. Pendant longtemps, il était admis que ces nutriments étaient détectés uniquement via leurs… (more)

Subjects/Keywords: CD36; GPR120; Goût; Lipides; Préférence; Régulation; GLP-1; Obésité; CD36; GPR120; Taste; Fat; Preference; Regulation; GLP-1; Obesity; 572; 573

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

APA (6th Edition):

Martin, C. (2011). Détection gustative des lipides alimentaires chez la souris : portrait croisé de deux lipido-récepteurs, CD36 & GPR120 : impacts sur les préférences alimentaires et la santé : Gustatory detection of dietary lipids in the mouse : crossed portrait of two lipid-sensors CD36 & GPR120 : impacts on food preferences and health. (Doctoral Dissertation). Université de Bourgogne. Retrieved from http://www.theses.fr/2011DIJOS077

Chicago Manual of Style (16th Edition):

Martin, Céline. “Détection gustative des lipides alimentaires chez la souris : portrait croisé de deux lipido-récepteurs, CD36 & GPR120 : impacts sur les préférences alimentaires et la santé : Gustatory detection of dietary lipids in the mouse : crossed portrait of two lipid-sensors CD36 & GPR120 : impacts on food preferences and health.” 2011. Doctoral Dissertation, Université de Bourgogne. Accessed October 23, 2019. http://www.theses.fr/2011DIJOS077.

MLA Handbook (7th Edition):

Martin, Céline. “Détection gustative des lipides alimentaires chez la souris : portrait croisé de deux lipido-récepteurs, CD36 & GPR120 : impacts sur les préférences alimentaires et la santé : Gustatory detection of dietary lipids in the mouse : crossed portrait of two lipid-sensors CD36 & GPR120 : impacts on food preferences and health.” 2011. Web. 23 Oct 2019.

Vancouver:

Martin C. Détection gustative des lipides alimentaires chez la souris : portrait croisé de deux lipido-récepteurs, CD36 & GPR120 : impacts sur les préférences alimentaires et la santé : Gustatory detection of dietary lipids in the mouse : crossed portrait of two lipid-sensors CD36 & GPR120 : impacts on food preferences and health. [Internet] [Doctoral dissertation]. Université de Bourgogne; 2011. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2011DIJOS077.

Council of Science Editors:

Martin C. Détection gustative des lipides alimentaires chez la souris : portrait croisé de deux lipido-récepteurs, CD36 & GPR120 : impacts sur les préférences alimentaires et la santé : Gustatory detection of dietary lipids in the mouse : crossed portrait of two lipid-sensors CD36 & GPR120 : impacts on food preferences and health. [Doctoral Dissertation]. Université de Bourgogne; 2011. Available from: http://www.theses.fr/2011DIJOS077

19. Lasalle, Manuel. TGR5, cible thérapeutique pour le traitement du diabète de type 2 et ses complications métaboliques : de la chimie aux effets biologiques : TGR5, therapeutic target for the treatment of diabetes mellitus and its metabolic complications : from chemistry to biological effects.

Degree: Docteur es, Sciences du médicament, 2015, Université Lille II – Droit et Santé

 Les acides biliaires sont depuis longtemps connus pour leur propriété d’agents solubilisant des graisses et des vitamines liposolubles, permettant ainsi une absorption efficace de ces… (more)

Subjects/Keywords: TGR5; Agoniste; Diabète; GLP-1; Incrétine; Topique; Kinétophore; TGR5; Agonist; Diabetes; GLP-1; Incretin; Topical; Kinetophore

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APA (6th Edition):

Lasalle, M. (2015). TGR5, cible thérapeutique pour le traitement du diabète de type 2 et ses complications métaboliques : de la chimie aux effets biologiques : TGR5, therapeutic target for the treatment of diabetes mellitus and its metabolic complications : from chemistry to biological effects. (Doctoral Dissertation). Université Lille II – Droit et Santé. Retrieved from http://www.theses.fr/2015LIL2S023

Chicago Manual of Style (16th Edition):

Lasalle, Manuel. “TGR5, cible thérapeutique pour le traitement du diabète de type 2 et ses complications métaboliques : de la chimie aux effets biologiques : TGR5, therapeutic target for the treatment of diabetes mellitus and its metabolic complications : from chemistry to biological effects.” 2015. Doctoral Dissertation, Université Lille II – Droit et Santé. Accessed October 23, 2019. http://www.theses.fr/2015LIL2S023.

MLA Handbook (7th Edition):

Lasalle, Manuel. “TGR5, cible thérapeutique pour le traitement du diabète de type 2 et ses complications métaboliques : de la chimie aux effets biologiques : TGR5, therapeutic target for the treatment of diabetes mellitus and its metabolic complications : from chemistry to biological effects.” 2015. Web. 23 Oct 2019.

Vancouver:

Lasalle M. TGR5, cible thérapeutique pour le traitement du diabète de type 2 et ses complications métaboliques : de la chimie aux effets biologiques : TGR5, therapeutic target for the treatment of diabetes mellitus and its metabolic complications : from chemistry to biological effects. [Internet] [Doctoral dissertation]. Université Lille II – Droit et Santé 2015. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2015LIL2S023.

Council of Science Editors:

Lasalle M. TGR5, cible thérapeutique pour le traitement du diabète de type 2 et ses complications métaboliques : de la chimie aux effets biologiques : TGR5, therapeutic target for the treatment of diabetes mellitus and its metabolic complications : from chemistry to biological effects. [Doctoral Dissertation]. Université Lille II – Droit et Santé 2015. Available from: http://www.theses.fr/2015LIL2S023

20. Hoguet, Vanessa. Optimisation de nouveaux agonistes topiques intestinaux du récepteur aux acides biliaires TGR5 pour le traitement du diabète de type 2 : Optimization of new topical intestinal agonists of the bile acid receptor TGR5 for the treatment of type 2 diabetes.

Degree: Docteur es, Sciences du médicament, 2017, Université Lille II – Droit et Santé

Le récepteur membranaire TGR5 (Takeda G Protein-coupled Receptor 5), est un récepteur ubiquitaire sensible aux acides biliaires. Il est exprimé dans de nombreux tissus et… (more)

Subjects/Keywords: TGR5; Agoniste; Topique intestinal; GLP-1; Incrétine; Kinétophore; TGR5; Agonist; Topical intestinal; GLP-1; Incretine; Kinetophore

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APA (6th Edition):

Hoguet, V. (2017). Optimisation de nouveaux agonistes topiques intestinaux du récepteur aux acides biliaires TGR5 pour le traitement du diabète de type 2 : Optimization of new topical intestinal agonists of the bile acid receptor TGR5 for the treatment of type 2 diabetes. (Doctoral Dissertation). Université Lille II – Droit et Santé. Retrieved from http://www.theses.fr/2017LIL2S024

Chicago Manual of Style (16th Edition):

Hoguet, Vanessa. “Optimisation de nouveaux agonistes topiques intestinaux du récepteur aux acides biliaires TGR5 pour le traitement du diabète de type 2 : Optimization of new topical intestinal agonists of the bile acid receptor TGR5 for the treatment of type 2 diabetes.” 2017. Doctoral Dissertation, Université Lille II – Droit et Santé. Accessed October 23, 2019. http://www.theses.fr/2017LIL2S024.

MLA Handbook (7th Edition):

Hoguet, Vanessa. “Optimisation de nouveaux agonistes topiques intestinaux du récepteur aux acides biliaires TGR5 pour le traitement du diabète de type 2 : Optimization of new topical intestinal agonists of the bile acid receptor TGR5 for the treatment of type 2 diabetes.” 2017. Web. 23 Oct 2019.

Vancouver:

Hoguet V. Optimisation de nouveaux agonistes topiques intestinaux du récepteur aux acides biliaires TGR5 pour le traitement du diabète de type 2 : Optimization of new topical intestinal agonists of the bile acid receptor TGR5 for the treatment of type 2 diabetes. [Internet] [Doctoral dissertation]. Université Lille II – Droit et Santé 2017. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2017LIL2S024.

Council of Science Editors:

Hoguet V. Optimisation de nouveaux agonistes topiques intestinaux du récepteur aux acides biliaires TGR5 pour le traitement du diabète de type 2 : Optimization of new topical intestinal agonists of the bile acid receptor TGR5 for the treatment of type 2 diabetes. [Doctoral Dissertation]. Université Lille II – Droit et Santé 2017. Available from: http://www.theses.fr/2017LIL2S024


Vrije Universiteit Amsterdam

21. Fineman, M.S. Development of immediate and sustained-release formulations of the glucagon-like peptide-1 receptor agonist exenatide for the treatment of patients with type 2 diabetes .

Degree: 2011, Vrije Universiteit Amsterdam

Subjects/Keywords: exenatide; GLP-1; GLP-1 receptor agonist; incretin therapy

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APA (6th Edition):

Fineman, M. S. (2011). Development of immediate and sustained-release formulations of the glucagon-like peptide-1 receptor agonist exenatide for the treatment of patients with type 2 diabetes . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/22344

Chicago Manual of Style (16th Edition):

Fineman, M S. “Development of immediate and sustained-release formulations of the glucagon-like peptide-1 receptor agonist exenatide for the treatment of patients with type 2 diabetes .” 2011. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed October 23, 2019. http://hdl.handle.net/1871/22344.

MLA Handbook (7th Edition):

Fineman, M S. “Development of immediate and sustained-release formulations of the glucagon-like peptide-1 receptor agonist exenatide for the treatment of patients with type 2 diabetes .” 2011. Web. 23 Oct 2019.

Vancouver:

Fineman MS. Development of immediate and sustained-release formulations of the glucagon-like peptide-1 receptor agonist exenatide for the treatment of patients with type 2 diabetes . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2011. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/1871/22344.

Council of Science Editors:

Fineman MS. Development of immediate and sustained-release formulations of the glucagon-like peptide-1 receptor agonist exenatide for the treatment of patients with type 2 diabetes . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2011. Available from: http://hdl.handle.net/1871/22344


Virginia Commonwealth University

22. May, Alexander T. Identification of Expression and Function of the Glucagon-like Peptide-1 Receptor in Gastrointestinal Smooth Muscle.

Degree: MS, Physiology and Biophysics, 2017, Virginia Commonwealth University

  In response to ingestion of nutrients, enteroendocrine L cells secrete the incretin hormone, glucagon-like peptide-1 (GLP-1), to enhance glucose-dependent insulin release. Therapies related to… (more)

Subjects/Keywords: GLP-1; gastrointestinal smooth muscle; GLP-1R; motility; relaxation; GLP-1 (7-36) amide; Biophysics; Cellular and Molecular Physiology; Digestive System; Endocrinology

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APA (6th Edition):

May, A. T. (2017). Identification of Expression and Function of the Glucagon-like Peptide-1 Receptor in Gastrointestinal Smooth Muscle. (Thesis). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/4886

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):

May, Alexander T. “Identification of Expression and Function of the Glucagon-like Peptide-1 Receptor in Gastrointestinal Smooth Muscle.” 2017. Thesis, Virginia Commonwealth University. Accessed October 23, 2019. https://scholarscompass.vcu.edu/etd/4886.

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

MLA Handbook (7th Edition):

May, Alexander T. “Identification of Expression and Function of the Glucagon-like Peptide-1 Receptor in Gastrointestinal Smooth Muscle.” 2017. Web. 23 Oct 2019.

Vancouver:

May AT. Identification of Expression and Function of the Glucagon-like Peptide-1 Receptor in Gastrointestinal Smooth Muscle. [Internet] [Thesis]. Virginia Commonwealth University; 2017. [cited 2019 Oct 23]. Available from: https://scholarscompass.vcu.edu/etd/4886.

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

Council of Science Editors:

May AT. Identification of Expression and Function of the Glucagon-like Peptide-1 Receptor in Gastrointestinal Smooth Muscle. [Thesis]. Virginia Commonwealth University; 2017. Available from: https://scholarscompass.vcu.edu/etd/4886

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

23. Mascali, Loriana Grazia Vanessa. Caratterizzazione della funzione e del comportamento dell'alfa cellula pancreatica: analisi dei meccanismi fisiopatologici implicati nell'insorgenza del diabete.

Degree: 2013, Università degli Studi di Catania

 Le alfa cellule pancreatiche in corso di diabete producono glucagone in maniera inappropriata, senza risentire dell effetto inibitorio dell insulina. Lo scopo dello studio è… (more)

Subjects/Keywords: Area 06 - Scienze mediche; alpha cells, Palmitate, GLP-1, Silencing, cytokine

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APA (6th Edition):

Mascali, L. G. V. (2013). Caratterizzazione della funzione e del comportamento dell'alfa cellula pancreatica: analisi dei meccanismi fisiopatologici implicati nell'insorgenza del diabete. (Thesis). Università degli Studi di Catania. Retrieved from http://hdl.handle.net/10761/1459

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):

Mascali, Loriana Grazia Vanessa. “Caratterizzazione della funzione e del comportamento dell'alfa cellula pancreatica: analisi dei meccanismi fisiopatologici implicati nell'insorgenza del diabete.” 2013. Thesis, Università degli Studi di Catania. Accessed October 23, 2019. http://hdl.handle.net/10761/1459.

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

MLA Handbook (7th Edition):

Mascali, Loriana Grazia Vanessa. “Caratterizzazione della funzione e del comportamento dell'alfa cellula pancreatica: analisi dei meccanismi fisiopatologici implicati nell'insorgenza del diabete.” 2013. Web. 23 Oct 2019.

Vancouver:

Mascali LGV. Caratterizzazione della funzione e del comportamento dell'alfa cellula pancreatica: analisi dei meccanismi fisiopatologici implicati nell'insorgenza del diabete. [Internet] [Thesis]. Università degli Studi di Catania; 2013. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10761/1459.

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

Council of Science Editors:

Mascali LGV. Caratterizzazione della funzione e del comportamento dell'alfa cellula pancreatica: analisi dei meccanismi fisiopatologici implicati nell'insorgenza del diabete. [Thesis]. Università degli Studi di Catania; 2013. Available from: http://hdl.handle.net/10761/1459

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


University of Alberta

24. Kolic, Jelena. Distinct Roles of Class 1 PI3K Isoforms in the Regulation of Beta Cell Exocytosis and Insulin Secretion.

Degree: PhD, Department of Pharmacology, 2014, University of Alberta

 Type 2 diabetes (T2D) is characterized by peripheral insulin resistance and an insufficiency of insulin secretion from the pancreatic beta cell. The incidence of T2D… (more)

Subjects/Keywords: PI3K; Beta cell; Insulin secretion; Exocytosis; GIP; GLP-1

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APA (6th Edition):

Kolic, J. (2014). Distinct Roles of Class 1 PI3K Isoforms in the Regulation of Beta Cell Exocytosis and Insulin Secretion. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/cft848q912

Chicago Manual of Style (16th Edition):

Kolic, Jelena. “Distinct Roles of Class 1 PI3K Isoforms in the Regulation of Beta Cell Exocytosis and Insulin Secretion.” 2014. Doctoral Dissertation, University of Alberta. Accessed October 23, 2019. https://era.library.ualberta.ca/files/cft848q912.

MLA Handbook (7th Edition):

Kolic, Jelena. “Distinct Roles of Class 1 PI3K Isoforms in the Regulation of Beta Cell Exocytosis and Insulin Secretion.” 2014. Web. 23 Oct 2019.

Vancouver:

Kolic J. Distinct Roles of Class 1 PI3K Isoforms in the Regulation of Beta Cell Exocytosis and Insulin Secretion. [Internet] [Doctoral dissertation]. University of Alberta; 2014. [cited 2019 Oct 23]. Available from: https://era.library.ualberta.ca/files/cft848q912.

Council of Science Editors:

Kolic J. Distinct Roles of Class 1 PI3K Isoforms in the Regulation of Beta Cell Exocytosis and Insulin Secretion. [Doctoral Dissertation]. University of Alberta; 2014. Available from: https://era.library.ualberta.ca/files/cft848q912


RMIT University

25. Wazzan, H. Regulation of glucagon-like peptide-1 (GLP-1) by milk protein fractions: an in vitro analysis.

Degree: 2018, RMIT University

 Obesity and diabetes are metabolic syndrome associated diseases. Increased body weight has been noticed worldwide and the World Health Organization (WHO) considers this as an… (more)

Subjects/Keywords: Fields of Research; Obesity; GLP-1; Satiety; Appetite; Milk Protein

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

APA (6th Edition):

Wazzan, H. (2018). Regulation of glucagon-like peptide-1 (GLP-1) by milk protein fractions: an in vitro analysis. (Thesis). RMIT University. Retrieved from http://researchbank.rmit.edu.au/view/rmit:162433

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):

Wazzan, H. “Regulation of glucagon-like peptide-1 (GLP-1) by milk protein fractions: an in vitro analysis.” 2018. Thesis, RMIT University. Accessed October 23, 2019. http://researchbank.rmit.edu.au/view/rmit:162433.

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

MLA Handbook (7th Edition):

Wazzan, H. “Regulation of glucagon-like peptide-1 (GLP-1) by milk protein fractions: an in vitro analysis.” 2018. Web. 23 Oct 2019.

Vancouver:

Wazzan H. Regulation of glucagon-like peptide-1 (GLP-1) by milk protein fractions: an in vitro analysis. [Internet] [Thesis]. RMIT University; 2018. [cited 2019 Oct 23]. Available from: http://researchbank.rmit.edu.au/view/rmit:162433.

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

Council of Science Editors:

Wazzan H. Regulation of glucagon-like peptide-1 (GLP-1) by milk protein fractions: an in vitro analysis. [Thesis]. RMIT University; 2018. Available from: http://researchbank.rmit.edu.au/view/rmit:162433

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


University of Cincinnati

26. Barrera, Jason G. The Role of Central Nervous System Glucagon-Like Peptide-1 in the Regulation of Energy Balance.

Degree: PhD, Medicine : Neuroscience/Medical Science Scholars Interdisiplinary, 2009, University of Cincinnati

  Glucagon-like peptide-1 (GLP-1), a product of the preproglucagon (PPG) gene, is synthesized in the intestine and the nucleus of the solitary tract (NTS) and… (more)

Subjects/Keywords: Neurology; CNS; preproglucagon; GLP-1; exendin; body weight; food intake

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

APA (6th Edition):

Barrera, J. G. (2009). The Role of Central Nervous System Glucagon-Like Peptide-1 in the Regulation of Energy Balance. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1258741489

Chicago Manual of Style (16th Edition):

Barrera, Jason G. “The Role of Central Nervous System Glucagon-Like Peptide-1 in the Regulation of Energy Balance.” 2009. Doctoral Dissertation, University of Cincinnati. Accessed October 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1258741489.

MLA Handbook (7th Edition):

Barrera, Jason G. “The Role of Central Nervous System Glucagon-Like Peptide-1 in the Regulation of Energy Balance.” 2009. Web. 23 Oct 2019.

Vancouver:

Barrera JG. The Role of Central Nervous System Glucagon-Like Peptide-1 in the Regulation of Energy Balance. [Internet] [Doctoral dissertation]. University of Cincinnati; 2009. [cited 2019 Oct 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1258741489.

Council of Science Editors:

Barrera JG. The Role of Central Nervous System Glucagon-Like Peptide-1 in the Regulation of Energy Balance. [Doctoral Dissertation]. University of Cincinnati; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1258741489


University of Gothenburg / Göteborgs Universitet

27. Anesten, Fredrik. IL-6 and GLP-1 in body fat regulating parts of the CNS in healthy mice.

Degree: 2016, University of Gothenburg / Göteborgs Universitet

 It has previously been shown that mice lacking interleukin-6 (IL-6) develop mature onset obesity. The weight-suppressing effects of IL-6 have been assumed to be exerted… (more)

Subjects/Keywords: IL-6; IL-6Rα; GLP-1; obesity; hypothalamus; brainstem; tanycytes; immunohistochemistry

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

APA (6th Edition):

Anesten, F. (2016). IL-6 and GLP-1 in body fat regulating parts of the CNS in healthy mice. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/41238

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):

Anesten, Fredrik. “IL-6 and GLP-1 in body fat regulating parts of the CNS in healthy mice.” 2016. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed October 23, 2019. http://hdl.handle.net/2077/41238.

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

MLA Handbook (7th Edition):

Anesten, Fredrik. “IL-6 and GLP-1 in body fat regulating parts of the CNS in healthy mice.” 2016. Web. 23 Oct 2019.

Vancouver:

Anesten F. IL-6 and GLP-1 in body fat regulating parts of the CNS in healthy mice. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2016. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/2077/41238.

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

Council of Science Editors:

Anesten F. IL-6 and GLP-1 in body fat regulating parts of the CNS in healthy mice. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2016. Available from: http://hdl.handle.net/2077/41238

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

28. Alexiadou, Kleopatra. Σύγκριση της επίδρασης της σιταγλιπτίνης και της μετφορμίνης στα επίπεδα των πεπτιδίων που ρυθμίζουν την όρεξη σε ασθενείς με διαβήτη τύπου 2.

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

Objective: To investigate the effect of sitagliptin and metformin on the gut peptide levels and on the glucose and lipid profiles in patients with type… (more)

Subjects/Keywords: Σιταγλιπτίνη; Μετφορμίνη; Ινκρετίνες; Sitagliptin; Metformin; Incretins; GLP-1; PYY

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

APA (6th Edition):

Alexiadou, K. (2014). Σύγκριση της επίδρασης της σιταγλιπτίνης και της μετφορμίνης στα επίπεδα των πεπτιδίων που ρυθμίζουν την όρεξη σε ασθενείς με διαβήτη τύπου 2. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/41995

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):

Alexiadou, Kleopatra. “Σύγκριση της επίδρασης της σιταγλιπτίνης και της μετφορμίνης στα επίπεδα των πεπτιδίων που ρυθμίζουν την όρεξη σε ασθενείς με διαβήτη τύπου 2.” 2014. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed October 23, 2019. http://hdl.handle.net/10442/hedi/41995.

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

MLA Handbook (7th Edition):

Alexiadou, Kleopatra. “Σύγκριση της επίδρασης της σιταγλιπτίνης και της μετφορμίνης στα επίπεδα των πεπτιδίων που ρυθμίζουν την όρεξη σε ασθενείς με διαβήτη τύπου 2.” 2014. Web. 23 Oct 2019.

Vancouver:

Alexiadou K. Σύγκριση της επίδρασης της σιταγλιπτίνης και της μετφορμίνης στα επίπεδα των πεπτιδίων που ρυθμίζουν την όρεξη σε ασθενείς με διαβήτη τύπου 2. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10442/hedi/41995.

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

Council of Science Editors:

Alexiadou K. Σύγκριση της επίδρασης της σιταγλιπτίνης και της μετφορμίνης στα επίπεδα των πεπτιδίων που ρυθμίζουν την όρεξη σε ασθενείς με διαβήτη τύπου 2. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. Available from: http://hdl.handle.net/10442/hedi/41995

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


University of Manchester

29. Wright, Elizabeth Joanne. GLP-1 CellBead therapy for the prevention of left ventricular dysfunction in pigs.

Degree: PhD, 2013, University of Manchester

 Background: Stem cells are a promising therapy for regeneration following myocardial infarction (MI). Another therapy currently under investigation for MI is glucagon-like peptide-1 (GLP-1), a… (more)

Subjects/Keywords: 616.1; Myocardial infarction; Mesenchymal stem cells; GLP-1

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

APA (6th Edition):

Wright, E. J. (2013). GLP-1 CellBead therapy for the prevention of left ventricular dysfunction in pigs. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/glp1-cellbead-therapy-for-the-prevention-of-left-ventricular-dysfunction-in-pigs(740704bb-46f1-44af-8eb2-22117a7efd05).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607399

Chicago Manual of Style (16th Edition):

Wright, Elizabeth Joanne. “GLP-1 CellBead therapy for the prevention of left ventricular dysfunction in pigs.” 2013. Doctoral Dissertation, University of Manchester. Accessed October 23, 2019. https://www.research.manchester.ac.uk/portal/en/theses/glp1-cellbead-therapy-for-the-prevention-of-left-ventricular-dysfunction-in-pigs(740704bb-46f1-44af-8eb2-22117a7efd05).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607399.

MLA Handbook (7th Edition):

Wright, Elizabeth Joanne. “GLP-1 CellBead therapy for the prevention of left ventricular dysfunction in pigs.” 2013. Web. 23 Oct 2019.

Vancouver:

Wright EJ. GLP-1 CellBead therapy for the prevention of left ventricular dysfunction in pigs. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2019 Oct 23]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/glp1-cellbead-therapy-for-the-prevention-of-left-ventricular-dysfunction-in-pigs(740704bb-46f1-44af-8eb2-22117a7efd05).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607399.

Council of Science Editors:

Wright EJ. GLP-1 CellBead therapy for the prevention of left ventricular dysfunction in pigs. [Doctoral Dissertation]. University of Manchester; 2013. Available from: https://www.research.manchester.ac.uk/portal/en/theses/glp1-cellbead-therapy-for-the-prevention-of-left-ventricular-dysfunction-in-pigs(740704bb-46f1-44af-8eb2-22117a7efd05).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607399


UCLA

30. Coveleskie, Kristen. The Impact of GLP-1 Analog, Exenatide, on The Resting Brain of Lean vs Obese Women.

Degree: Molec, Cell, & Integ Physiology, 2016, UCLA

 Obesity is a growing problem both in The United States and world-wide and women in The United States have the highest mean body mass index… (more)

Subjects/Keywords: Physiology; Neurosciences; Brain; fMRI; GLP-1; Obesity; Resting State

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

APA (6th Edition):

Coveleskie, K. (2016). The Impact of GLP-1 Analog, Exenatide, on The Resting Brain of Lean vs Obese Women. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/4zt480d8

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):

Coveleskie, Kristen. “The Impact of GLP-1 Analog, Exenatide, on The Resting Brain of Lean vs Obese Women.” 2016. Thesis, UCLA. Accessed October 23, 2019. http://www.escholarship.org/uc/item/4zt480d8.

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

MLA Handbook (7th Edition):

Coveleskie, Kristen. “The Impact of GLP-1 Analog, Exenatide, on The Resting Brain of Lean vs Obese Women.” 2016. Web. 23 Oct 2019.

Vancouver:

Coveleskie K. The Impact of GLP-1 Analog, Exenatide, on The Resting Brain of Lean vs Obese Women. [Internet] [Thesis]. UCLA; 2016. [cited 2019 Oct 23]. Available from: http://www.escholarship.org/uc/item/4zt480d8.

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

Council of Science Editors:

Coveleskie K. The Impact of GLP-1 Analog, Exenatide, on The Resting Brain of Lean vs Obese Women. [Thesis]. UCLA; 2016. Available from: http://www.escholarship.org/uc/item/4zt480d8

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

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