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You searched for subject:(insulin secretion). Showing records 1 – 30 of 175 total matches.

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University of Hong Kong

1. Hu, Xin. Pyruvate carboxylase is a downstream target of p53 in regulating insulin secretion.

Degree: Master of Medical Sciences, 2014, University of Hong Kong

Pyruvate carboxylase (PC), converting pyruvate to oxaloacetate (OAA), is a critical contributor to anaplerosis in pancreatic β-cell, the process that can replenish the intermediates in… (more)

Subjects/Keywords: Insulin - Secretion; Tumor proteins

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APA (6th Edition):

Hu, X. (2014). Pyruvate carboxylase is a downstream target of p53 in regulating insulin secretion. (Masters Thesis). University of Hong Kong. Retrieved from Hu, X. [胡欣]. (2014). Pyruvate carboxylase is a downstream target of p53 in regulating insulin secretion. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5394369 ; http://dx.doi.org/10.5353/th_b5394369 ; http://hdl.handle.net/10722/209538

Chicago Manual of Style (16th Edition):

Hu, Xin. “Pyruvate carboxylase is a downstream target of p53 in regulating insulin secretion.” 2014. Masters Thesis, University of Hong Kong. Accessed September 19, 2019. Hu, X. [胡欣]. (2014). Pyruvate carboxylase is a downstream target of p53 in regulating insulin secretion. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5394369 ; http://dx.doi.org/10.5353/th_b5394369 ; http://hdl.handle.net/10722/209538.

MLA Handbook (7th Edition):

Hu, Xin. “Pyruvate carboxylase is a downstream target of p53 in regulating insulin secretion.” 2014. Web. 19 Sep 2019.

Vancouver:

Hu X. Pyruvate carboxylase is a downstream target of p53 in regulating insulin secretion. [Internet] [Masters thesis]. University of Hong Kong; 2014. [cited 2019 Sep 19]. Available from: Hu, X. [胡欣]. (2014). Pyruvate carboxylase is a downstream target of p53 in regulating insulin secretion. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5394369 ; http://dx.doi.org/10.5353/th_b5394369 ; http://hdl.handle.net/10722/209538.

Council of Science Editors:

Hu X. Pyruvate carboxylase is a downstream target of p53 in regulating insulin secretion. [Masters Thesis]. University of Hong Kong; 2014. Available from: Hu, X. [胡欣]. (2014). Pyruvate carboxylase is a downstream target of p53 in regulating insulin secretion. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5394369 ; http://dx.doi.org/10.5353/th_b5394369 ; http://hdl.handle.net/10722/209538


University of Manchester

2. Basalem, Osama Salem. Congenital Hyperinsulinism; Effects of Rapamycin on Min6 Pancreatic β-Cell Line.

Degree: 2016, University of Manchester

Introduction: Congenital Hyperinsulinism (CHI) is a rare neonatal syndrome associated with continuous inappropriate insulin secretion by the pancreatic β-cell in the presence of recurring hypoglycemia.… (more)

Subjects/Keywords: Insulin secretion; Rapamycin; mTOR

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APA (6th Edition):

Basalem, O. S. (2016). Congenital Hyperinsulinism; Effects of Rapamycin on Min6 Pancreatic β-Cell Line. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:305154

Chicago Manual of Style (16th Edition):

Basalem, Osama Salem. “Congenital Hyperinsulinism; Effects of Rapamycin on Min6 Pancreatic β-Cell Line.” 2016. Doctoral Dissertation, University of Manchester. Accessed September 19, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:305154.

MLA Handbook (7th Edition):

Basalem, Osama Salem. “Congenital Hyperinsulinism; Effects of Rapamycin on Min6 Pancreatic β-Cell Line.” 2016. Web. 19 Sep 2019.

Vancouver:

Basalem OS. Congenital Hyperinsulinism; Effects of Rapamycin on Min6 Pancreatic β-Cell Line. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Sep 19]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:305154.

Council of Science Editors:

Basalem OS. Congenital Hyperinsulinism; Effects of Rapamycin on Min6 Pancreatic β-Cell Line. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:305154


Univerzitet u Beogradu

3. Cvijović, Goran M., 1971-. Sekrecija insulina i insulinska senzitivnost perifernih tkiva pre i nakon radikalnog lečenja primarnog hiperparatireoidizma.

Degree: Medicinski fakultet, 2016, Univerzitet u Beogradu

INTERNA MEDICINA - ENDOKRINOLOGIJA / INTERNAL MEDICINE - ENDOCRINOLOGY

Uvod i cilj: Prethodno je uočeno postojanje insulinske rezistencije i povećana prevalenca oštećene tolerancije na glikozu… (more)

Subjects/Keywords: primary hyperparathyroidism; insulin sensitivity; insulin secretion

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APA (6th Edition):

Cvijović, Goran M., 1. (2016). Sekrecija insulina i insulinska senzitivnost perifernih tkiva pre i nakon radikalnog lečenja primarnog hiperparatireoidizma. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:12592/bdef:Content/get

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):

Cvijović, Goran M., 1971-. “Sekrecija insulina i insulinska senzitivnost perifernih tkiva pre i nakon radikalnog lečenja primarnog hiperparatireoidizma.” 2016. Thesis, Univerzitet u Beogradu. Accessed September 19, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:12592/bdef:Content/get.

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

MLA Handbook (7th Edition):

Cvijović, Goran M., 1971-. “Sekrecija insulina i insulinska senzitivnost perifernih tkiva pre i nakon radikalnog lečenja primarnog hiperparatireoidizma.” 2016. Web. 19 Sep 2019.

Vancouver:

Cvijović, Goran M. 1. Sekrecija insulina i insulinska senzitivnost perifernih tkiva pre i nakon radikalnog lečenja primarnog hiperparatireoidizma. [Internet] [Thesis]. Univerzitet u Beogradu; 2016. [cited 2019 Sep 19]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:12592/bdef:Content/get.

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

Council of Science Editors:

Cvijović, Goran M. 1. Sekrecija insulina i insulinska senzitivnost perifernih tkiva pre i nakon radikalnog lečenja primarnog hiperparatireoidizma. [Thesis]. Univerzitet u Beogradu; 2016. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:12592/bdef:Content/get

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


Georgia State University

4. Kloc, Noreen. Insulin Dynamic Measures and Weight Change.

Degree: MPH, Public Health, 2016, Georgia State University

  ABSTRACT Insulin Dynamic Measures and Weight Change By Noreen Kloc B.S. Computer Information Technology, Purdue University December 7, 2015 INTRODUCTION: Weight gain and obesity… (more)

Subjects/Keywords: insulin resistance; insulin sensitivity; insulin secretion; weight; metabolic syndrome; diabetes

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APA (6th Edition):

Kloc, N. (2016). Insulin Dynamic Measures and Weight Change. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/iph_theses/437

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):

Kloc, Noreen. “Insulin Dynamic Measures and Weight Change.” 2016. Thesis, Georgia State University. Accessed September 19, 2019. https://scholarworks.gsu.edu/iph_theses/437.

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

MLA Handbook (7th Edition):

Kloc, Noreen. “Insulin Dynamic Measures and Weight Change.” 2016. Web. 19 Sep 2019.

Vancouver:

Kloc N. Insulin Dynamic Measures and Weight Change. [Internet] [Thesis]. Georgia State University; 2016. [cited 2019 Sep 19]. Available from: https://scholarworks.gsu.edu/iph_theses/437.

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

Council of Science Editors:

Kloc N. Insulin Dynamic Measures and Weight Change. [Thesis]. Georgia State University; 2016. Available from: https://scholarworks.gsu.edu/iph_theses/437

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


Wright State University

5. Alshahrani, Saeed. Role of Na+K+2Cl¿¿¿¿¿¿¿ Co-transporters in Insulin Secretion.

Degree: MS, Pharmacology and Toxicology, 2012, Wright State University

  The objective of this study is to investigate the role of intracellular chloride concentration ([Cl¿¿¿¿¿¿]i) in insulin secretion in vivo and in vitro. The… (more)

Subjects/Keywords: Pharmacology; &946; -cell, Insulin Secretion, NKCC1, NKCC2

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APA (6th Edition):

Alshahrani, S. (2012). Role of Na+K+2Cl¿¿¿¿¿¿¿ Co-transporters in Insulin Secretion. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1347832847

Chicago Manual of Style (16th Edition):

Alshahrani, Saeed. “Role of Na+K+2Cl¿¿¿¿¿¿¿ Co-transporters in Insulin Secretion.” 2012. Masters Thesis, Wright State University. Accessed September 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=wright1347832847.

MLA Handbook (7th Edition):

Alshahrani, Saeed. “Role of Na+K+2Cl¿¿¿¿¿¿¿ Co-transporters in Insulin Secretion.” 2012. Web. 19 Sep 2019.

Vancouver:

Alshahrani S. Role of Na+K+2Cl¿¿¿¿¿¿¿ Co-transporters in Insulin Secretion. [Internet] [Masters thesis]. Wright State University; 2012. [cited 2019 Sep 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1347832847.

Council of Science Editors:

Alshahrani S. Role of Na+K+2Cl¿¿¿¿¿¿¿ Co-transporters in Insulin Secretion. [Masters Thesis]. Wright State University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1347832847

6. Moin Abu Saleh Md. Neuroendocrine regulatory peptide-2 stimulates glucose-induced insulin secretion in vivo and in vitro.

Degree: 博士(医学), 2015, University of Miyazaki / 宮崎大学

以下に掲載:Biochemical and Biophysical Research Communications. November 2012, Volume 428, Issue 4, Pages 512–517, doi:10.1016/j.bbrc.2012.10.073.

Subjects/Keywords: NERP-2; Insulin secretion; Ca^<; 2+>

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APA (6th Edition):

Md., M. A. S. (2015). Neuroendocrine regulatory peptide-2 stimulates glucose-induced insulin secretion in vivo and in vitro. (Thesis). University of Miyazaki / 宮崎大学. Retrieved from http://hdl.handle.net/10458/5418

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):

Md., Moin Abu Saleh. “Neuroendocrine regulatory peptide-2 stimulates glucose-induced insulin secretion in vivo and in vitro.” 2015. Thesis, University of Miyazaki / 宮崎大学. Accessed September 19, 2019. http://hdl.handle.net/10458/5418.

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

MLA Handbook (7th Edition):

Md., Moin Abu Saleh. “Neuroendocrine regulatory peptide-2 stimulates glucose-induced insulin secretion in vivo and in vitro.” 2015. Web. 19 Sep 2019.

Vancouver:

Md. MAS. Neuroendocrine regulatory peptide-2 stimulates glucose-induced insulin secretion in vivo and in vitro. [Internet] [Thesis]. University of Miyazaki / 宮崎大学; 2015. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/10458/5418.

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

Council of Science Editors:

Md. MAS. Neuroendocrine regulatory peptide-2 stimulates glucose-induced insulin secretion in vivo and in vitro. [Thesis]. University of Miyazaki / 宮崎大学; 2015. Available from: http://hdl.handle.net/10458/5418

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


University of Edinburgh

7. Liu, Xiaoxia. Regulation and function of 11β-hydroxysteroid dehydrogenase (11β-HSD1) in pancreatic β-cells.

Degree: PhD, 2011, University of Edinburgh

 Diabetes Mellitus is characterized by high blood sugar and is caused by resistance to (type 2) or insufficiency of (type 1) the pancreatic β-cell hormone… (more)

Subjects/Keywords: 616.4; 11ß-HSD1; ß-cells; insulin; secretion

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APA (6th Edition):

Liu, X. (2011). Regulation and function of 11β-hydroxysteroid dehydrogenase (11β-HSD1) in pancreatic β-cells. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/5582

Chicago Manual of Style (16th Edition):

Liu, Xiaoxia. “Regulation and function of 11β-hydroxysteroid dehydrogenase (11β-HSD1) in pancreatic β-cells.” 2011. Doctoral Dissertation, University of Edinburgh. Accessed September 19, 2019. http://hdl.handle.net/1842/5582.

MLA Handbook (7th Edition):

Liu, Xiaoxia. “Regulation and function of 11β-hydroxysteroid dehydrogenase (11β-HSD1) in pancreatic β-cells.” 2011. Web. 19 Sep 2019.

Vancouver:

Liu X. Regulation and function of 11β-hydroxysteroid dehydrogenase (11β-HSD1) in pancreatic β-cells. [Internet] [Doctoral dissertation]. University of Edinburgh; 2011. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/1842/5582.

Council of Science Editors:

Liu X. Regulation and function of 11β-hydroxysteroid dehydrogenase (11β-HSD1) in pancreatic β-cells. [Doctoral Dissertation]. University of Edinburgh; 2011. Available from: http://hdl.handle.net/1842/5582

8. Loweth, Anne C. Phospholipase A←2 expression and mechanisms of cell death in the endocrine pancreas.

Degree: PhD, 1995, Keele University

Subjects/Keywords: 572.8; Insulin secretion

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APA (6th Edition):

Loweth, A. C. (1995). Phospholipase A←2 expression and mechanisms of cell death in the endocrine pancreas. (Doctoral Dissertation). Keele University. Retrieved from https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.283255

Chicago Manual of Style (16th Edition):

Loweth, Anne C. “Phospholipase A←2 expression and mechanisms of cell death in the endocrine pancreas.” 1995. Doctoral Dissertation, Keele University. Accessed September 19, 2019. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.283255.

MLA Handbook (7th Edition):

Loweth, Anne C. “Phospholipase A←2 expression and mechanisms of cell death in the endocrine pancreas.” 1995. Web. 19 Sep 2019.

Vancouver:

Loweth AC. Phospholipase A←2 expression and mechanisms of cell death in the endocrine pancreas. [Internet] [Doctoral dissertation]. Keele University; 1995. [cited 2019 Sep 19]. Available from: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.283255.

Council of Science Editors:

Loweth AC. Phospholipase A←2 expression and mechanisms of cell death in the endocrine pancreas. [Doctoral Dissertation]. Keele University; 1995. Available from: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.283255


University of New South Wales

9. Pearson, Gemma. THE ROLE(S) OF LIPID SPECIES IN GLUCOSE-STIMULATED INSULIN SECRETION FROM PANCREATIC β-­CELLS.

Degree: Garvan Institute of Medical Research, 2014, University of New South Wales

 Glucose-stimulated insulin secretion (GSIS) from pancreatic β-cells is vital for whole-bodyglucose homeostasis, and loss of β-cell function can result in type 2 diabetes(T2D), a major… (more)

Subjects/Keywords: Lipids; Pancreatic beta cells; Insulin secretion; Lysosomes

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APA (6th Edition):

Pearson, G. (2014). THE ROLE(S) OF LIPID SPECIES IN GLUCOSE-STIMULATED INSULIN SECRETION FROM PANCREATIC β-­CELLS. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/53494 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12189/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Pearson, Gemma. “THE ROLE(S) OF LIPID SPECIES IN GLUCOSE-STIMULATED INSULIN SECRETION FROM PANCREATIC β-­CELLS.” 2014. Doctoral Dissertation, University of New South Wales. Accessed September 19, 2019. http://handle.unsw.edu.au/1959.4/53494 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12189/SOURCE02?view=true.

MLA Handbook (7th Edition):

Pearson, Gemma. “THE ROLE(S) OF LIPID SPECIES IN GLUCOSE-STIMULATED INSULIN SECRETION FROM PANCREATIC β-­CELLS.” 2014. Web. 19 Sep 2019.

Vancouver:

Pearson G. THE ROLE(S) OF LIPID SPECIES IN GLUCOSE-STIMULATED INSULIN SECRETION FROM PANCREATIC β-­CELLS. [Internet] [Doctoral dissertation]. University of New South Wales; 2014. [cited 2019 Sep 19]. Available from: http://handle.unsw.edu.au/1959.4/53494 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12189/SOURCE02?view=true.

Council of Science Editors:

Pearson G. THE ROLE(S) OF LIPID SPECIES IN GLUCOSE-STIMULATED INSULIN SECRETION FROM PANCREATIC β-­CELLS. [Doctoral Dissertation]. University of New South Wales; 2014. Available from: http://handle.unsw.edu.au/1959.4/53494 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12189/SOURCE02?view=true

10. El Azzouny, Mahmoud. Development and Application of Metabolomics Techniques to Improve Understanding of Glucose and Fatty Acid Metabolism in ß-cells and their Role in Insulin Secretion.

Degree: PhD, Chemistry, 2014, University of Michigan

 The primary function of pancreatic beta cells is to secrete insulin in response to glucose metabolism. Decline in beta cell function contributes to the development… (more)

Subjects/Keywords: Metabolomics; Glucose Stimulated Insulin Secretion; Chemistry; Science

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APA (6th Edition):

El Azzouny, M. (2014). Development and Application of Metabolomics Techniques to Improve Understanding of Glucose and Fatty Acid Metabolism in ß-cells and their Role in Insulin Secretion. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/107168

Chicago Manual of Style (16th Edition):

El Azzouny, Mahmoud. “Development and Application of Metabolomics Techniques to Improve Understanding of Glucose and Fatty Acid Metabolism in ß-cells and their Role in Insulin Secretion.” 2014. Doctoral Dissertation, University of Michigan. Accessed September 19, 2019. http://hdl.handle.net/2027.42/107168.

MLA Handbook (7th Edition):

El Azzouny, Mahmoud. “Development and Application of Metabolomics Techniques to Improve Understanding of Glucose and Fatty Acid Metabolism in ß-cells and their Role in Insulin Secretion.” 2014. Web. 19 Sep 2019.

Vancouver:

El Azzouny M. Development and Application of Metabolomics Techniques to Improve Understanding of Glucose and Fatty Acid Metabolism in ß-cells and their Role in Insulin Secretion. [Internet] [Doctoral dissertation]. University of Michigan; 2014. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/2027.42/107168.

Council of Science Editors:

El Azzouny M. Development and Application of Metabolomics Techniques to Improve Understanding of Glucose and Fatty Acid Metabolism in ß-cells and their Role in Insulin Secretion. [Doctoral Dissertation]. University of Michigan; 2014. Available from: http://hdl.handle.net/2027.42/107168


University of Toronto

11. Koo, Ellen. Syntaxin-3 Regulates Biphasic Glucose Stimulated Insulin Secretion in the Pancreatic Beta Cell.

Degree: 2010, University of Toronto

Our study aims to investigate the role of Syntaxin-3 in glucose stimulated insulin secretion (GSIS) and how it regulates the recruitment to plasma membrane and/or… (more)

Subjects/Keywords: Insulin Secretion; Syntaxin; SNAREs; Exocytosis; 0719

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APA (6th Edition):

Koo, E. (2010). Syntaxin-3 Regulates Biphasic Glucose Stimulated Insulin Secretion in the Pancreatic Beta Cell. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25732

Chicago Manual of Style (16th Edition):

Koo, Ellen. “Syntaxin-3 Regulates Biphasic Glucose Stimulated Insulin Secretion in the Pancreatic Beta Cell.” 2010. Masters Thesis, University of Toronto. Accessed September 19, 2019. http://hdl.handle.net/1807/25732.

MLA Handbook (7th Edition):

Koo, Ellen. “Syntaxin-3 Regulates Biphasic Glucose Stimulated Insulin Secretion in the Pancreatic Beta Cell.” 2010. Web. 19 Sep 2019.

Vancouver:

Koo E. Syntaxin-3 Regulates Biphasic Glucose Stimulated Insulin Secretion in the Pancreatic Beta Cell. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/1807/25732.

Council of Science Editors:

Koo E. Syntaxin-3 Regulates Biphasic Glucose Stimulated Insulin Secretion in the Pancreatic Beta Cell. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25732

12. Burns, Christian Henry. Characterization of VPS41 and its Role in the Regulated Secretory Pathway.

Degree: MS, Biological Sciences, 2019, U of Denver

Insulin secretory granules (SGs) mediate the regulated secretion of insulin, which is essential for glucose homeostasis. The basic machinery responsible for this regulated exocytosis… (more)

Subjects/Keywords: Diabetes; HOPS; Insulin; Lysosome; Regulated Secretion; VPS41

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APA (6th Edition):

Burns, C. H. (2019). Characterization of VPS41 and its Role in the Regulated Secretory Pathway. (Thesis). U of Denver. Retrieved from https://digitalcommons.du.edu/etd/1567

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):

Burns, Christian Henry. “Characterization of VPS41 and its Role in the Regulated Secretory Pathway.” 2019. Thesis, U of Denver. Accessed September 19, 2019. https://digitalcommons.du.edu/etd/1567.

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

MLA Handbook (7th Edition):

Burns, Christian Henry. “Characterization of VPS41 and its Role in the Regulated Secretory Pathway.” 2019. Web. 19 Sep 2019.

Vancouver:

Burns CH. Characterization of VPS41 and its Role in the Regulated Secretory Pathway. [Internet] [Thesis]. U of Denver; 2019. [cited 2019 Sep 19]. Available from: https://digitalcommons.du.edu/etd/1567.

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

Council of Science Editors:

Burns CH. Characterization of VPS41 and its Role in the Regulated Secretory Pathway. [Thesis]. U of Denver; 2019. Available from: https://digitalcommons.du.edu/etd/1567

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


University of Lund

13. Dayeh, Tasnim. The Human Pancreatic Islet Methylome and Its Role in Type 2 Diabetes.

Degree: 2016, University of Lund

 Islet dysfunction is central to the development and progression of type 2 diabetes (T2D). Epigenetic modifications are essential for establishing and maintaining cell identity and… (more)

Subjects/Keywords: Endokrinologi och diabetes; CpG-SNP; glucagon secretion; insulin secretion; human pancreatic islets; DNA methylation; Epigenetics

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APA (6th Edition):

Dayeh, T. (2016). The Human Pancreatic Islet Methylome and Its Role in Type 2 Diabetes. (Doctoral Dissertation). University of Lund. Retrieved from http://lup.lub.lu.se/record/8515603 ; http://portal.research.lu.se/ws/files/3614834/8515627.pdf

Chicago Manual of Style (16th Edition):

Dayeh, Tasnim. “The Human Pancreatic Islet Methylome and Its Role in Type 2 Diabetes.” 2016. Doctoral Dissertation, University of Lund. Accessed September 19, 2019. http://lup.lub.lu.se/record/8515603 ; http://portal.research.lu.se/ws/files/3614834/8515627.pdf.

MLA Handbook (7th Edition):

Dayeh, Tasnim. “The Human Pancreatic Islet Methylome and Its Role in Type 2 Diabetes.” 2016. Web. 19 Sep 2019.

Vancouver:

Dayeh T. The Human Pancreatic Islet Methylome and Its Role in Type 2 Diabetes. [Internet] [Doctoral dissertation]. University of Lund; 2016. [cited 2019 Sep 19]. Available from: http://lup.lub.lu.se/record/8515603 ; http://portal.research.lu.se/ws/files/3614834/8515627.pdf.

Council of Science Editors:

Dayeh T. The Human Pancreatic Islet Methylome and Its Role in Type 2 Diabetes. [Doctoral Dissertation]. University of Lund; 2016. Available from: http://lup.lub.lu.se/record/8515603 ; http://portal.research.lu.se/ws/files/3614834/8515627.pdf


University of Florida

14. MONTERO,CINDY. The Effect of Epigallocatechin-Gallate on Adiponectin Expression and the Insulin Signaling Pathway.

Degree: MS, Food Science and Human Nutrition, 2011, University of Florida

 Adiponectin, a hormone secreted from adipocytes, in low circulating levels has been epidemiologically associated with obesity, insulin resistance, type 2 diabetes, and cardiovascular disease; it… (more)

Subjects/Keywords: Adipocytes; Gallates; Insulin; Insulin resistance; Obesity; Phosphorylation; Plasmas; Receptors; Secretion; Type 2 diabetes mellitus

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

APA (6th Edition):

MONTERO,CINDY. (2011). The Effect of Epigallocatechin-Gallate on Adiponectin Expression and the Insulin Signaling Pathway. (Masters Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0042647

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

MONTERO,CINDY. “The Effect of Epigallocatechin-Gallate on Adiponectin Expression and the Insulin Signaling Pathway.” 2011. Masters Thesis, University of Florida. Accessed September 19, 2019. http://ufdc.ufl.edu/UFE0042647.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

MONTERO,CINDY. “The Effect of Epigallocatechin-Gallate on Adiponectin Expression and the Insulin Signaling Pathway.” 2011. Web. 19 Sep 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

MONTERO,CINDY. The Effect of Epigallocatechin-Gallate on Adiponectin Expression and the Insulin Signaling Pathway. [Internet] [Masters thesis]. University of Florida; 2011. [cited 2019 Sep 19]. Available from: http://ufdc.ufl.edu/UFE0042647.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

MONTERO,CINDY. The Effect of Epigallocatechin-Gallate on Adiponectin Expression and the Insulin Signaling Pathway. [Masters Thesis]. University of Florida; 2011. Available from: http://ufdc.ufl.edu/UFE0042647

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


University of Western Ontario

15. Oakie, Amanda. The role of c-Kit and insulin receptor tyrosine kinases in beta cell function and insulin secretion.

Degree: 2019, University of Western Ontario

 The receptor tyrosine kinases (RTKs) c-Kit and insulin receptor (IR) initiate similar intracellular signalling pathways in pancreatic beta cells to regulate beta cell proliferation, survival,… (more)

Subjects/Keywords: c-Kit; insulin receptor; diabetes mellitus; insulin secretion; SNARE protein; Cre recombinase; Endocrinology

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

APA (6th Edition):

Oakie, A. (2019). The role of c-Kit and insulin receptor tyrosine kinases in beta cell function and insulin secretion. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/6232

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):

Oakie, Amanda. “The role of c-Kit and insulin receptor tyrosine kinases in beta cell function and insulin secretion.” 2019. Thesis, University of Western Ontario. Accessed September 19, 2019. https://ir.lib.uwo.ca/etd/6232.

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

MLA Handbook (7th Edition):

Oakie, Amanda. “The role of c-Kit and insulin receptor tyrosine kinases in beta cell function and insulin secretion.” 2019. Web. 19 Sep 2019.

Vancouver:

Oakie A. The role of c-Kit and insulin receptor tyrosine kinases in beta cell function and insulin secretion. [Internet] [Thesis]. University of Western Ontario; 2019. [cited 2019 Sep 19]. Available from: https://ir.lib.uwo.ca/etd/6232.

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

Council of Science Editors:

Oakie A. The role of c-Kit and insulin receptor tyrosine kinases in beta cell function and insulin secretion. [Thesis]. University of Western Ontario; 2019. Available from: https://ir.lib.uwo.ca/etd/6232

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


University of Alberta

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

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 September 19, 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. 19 Sep 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 Sep 19]. 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

17. Khalid, Parwaiz. Some biochemical studies on the islets of langerhans of rat pancreas with special reference to secretion of insulin;.

Degree: Biochemistry, 1988, Aligarh Muslim University

Abstract not available newline newline

Bibliography p. 135-160

Advisors/Committee Members: Kidwai, J R.

Subjects/Keywords: Biochemical; Secretion; Insulin; Langerhans; Pancreas

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APA (6th Edition):

Khalid, P. (1988). Some biochemical studies on the islets of langerhans of rat pancreas with special reference to secretion of insulin;. (Thesis). Aligarh Muslim University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/53889

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):

Khalid, Parwaiz. “Some biochemical studies on the islets of langerhans of rat pancreas with special reference to secretion of insulin;.” 1988. Thesis, Aligarh Muslim University. Accessed September 19, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/53889.

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

MLA Handbook (7th Edition):

Khalid, Parwaiz. “Some biochemical studies on the islets of langerhans of rat pancreas with special reference to secretion of insulin;.” 1988. Web. 19 Sep 2019.

Vancouver:

Khalid P. Some biochemical studies on the islets of langerhans of rat pancreas with special reference to secretion of insulin;. [Internet] [Thesis]. Aligarh Muslim University; 1988. [cited 2019 Sep 19]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/53889.

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

Council of Science Editors:

Khalid P. Some biochemical studies on the islets of langerhans of rat pancreas with special reference to secretion of insulin;. [Thesis]. Aligarh Muslim University; 1988. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/53889

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


Université de Montréal

18. Belson, Linda. Impact du sexe et du profil génétique sur la sécrétion d’insuline dans une cohorte de patients atteints de fibrose kystique .

Degree: 2013, Université de Montréal

 Introduction : La Fibrose Kystique (FK) est la maladie autosomique récessive la plus fréquente chez les Caucasiens et est due à une mutation du gène… (more)

Subjects/Keywords: Fibrose Kystique; Cystic Fibrosis; Diabète; Diabetes; Insuline; Insulin; Sécrétion; Secretion

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

APA (6th Edition):

Belson, L. (2013). Impact du sexe et du profil génétique sur la sécrétion d’insuline dans une cohorte de patients atteints de fibrose kystique . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/12745

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):

Belson, Linda. “Impact du sexe et du profil génétique sur la sécrétion d’insuline dans une cohorte de patients atteints de fibrose kystique .” 2013. Thesis, Université de Montréal. Accessed September 19, 2019. http://hdl.handle.net/1866/12745.

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

MLA Handbook (7th Edition):

Belson, Linda. “Impact du sexe et du profil génétique sur la sécrétion d’insuline dans une cohorte de patients atteints de fibrose kystique .” 2013. Web. 19 Sep 2019.

Vancouver:

Belson L. Impact du sexe et du profil génétique sur la sécrétion d’insuline dans une cohorte de patients atteints de fibrose kystique . [Internet] [Thesis]. Université de Montréal; 2013. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/1866/12745.

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

Council of Science Editors:

Belson L. Impact du sexe et du profil génétique sur la sécrétion d’insuline dans une cohorte de patients atteints de fibrose kystique . [Thesis]. Université de Montréal; 2013. Available from: http://hdl.handle.net/1866/12745

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


Dublin City University

19. Hennessy, Erica. Investigation of pancreatic beta cell differentiation and function, and global profiling analysis of diabetes serum for the identification of disease biomarkers.

Degree: School of Biotechnology; Dublin City University. National Institute for Cellular Biotechnology (NICB), 2012, Dublin City University

 This study aimed to investigate the molecular mechanisms of glucose stimulated insulin secretion (GSIS), specifically the role of microRNAs (miRNAs) in this process. TaqMan low… (more)

Subjects/Keywords: Biotechnology; Cell biology; glucose stimulated insulin secretion; GSIS; microRNAs; miRNAs

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

APA (6th Edition):

Hennessy, E. (2012). Investigation of pancreatic beta cell differentiation and function, and global profiling analysis of diabetes serum for the identification of disease biomarkers. (Thesis). Dublin City University. Retrieved from http://doras.dcu.ie/16787/

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):

Hennessy, Erica. “Investigation of pancreatic beta cell differentiation and function, and global profiling analysis of diabetes serum for the identification of disease biomarkers.” 2012. Thesis, Dublin City University. Accessed September 19, 2019. http://doras.dcu.ie/16787/.

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

MLA Handbook (7th Edition):

Hennessy, Erica. “Investigation of pancreatic beta cell differentiation and function, and global profiling analysis of diabetes serum for the identification of disease biomarkers.” 2012. Web. 19 Sep 2019.

Vancouver:

Hennessy E. Investigation of pancreatic beta cell differentiation and function, and global profiling analysis of diabetes serum for the identification of disease biomarkers. [Internet] [Thesis]. Dublin City University; 2012. [cited 2019 Sep 19]. Available from: http://doras.dcu.ie/16787/.

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

Council of Science Editors:

Hennessy E. Investigation of pancreatic beta cell differentiation and function, and global profiling analysis of diabetes serum for the identification of disease biomarkers. [Thesis]. Dublin City University; 2012. Available from: http://doras.dcu.ie/16787/

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

20. Farret, Anne. Effets et mécanismes de l'activation des récepteurs purinergiques P2Y de la cellule beta pancréatique : Effects and mechanisms of activation of P2Y purinergic receptors of the pancreatic beta cell.

Degree: Docteur es, Anesthésiologie, réanimation, médecine d'urgence, pharmacologie et thérapeutique, 2010, Université Montpellier I

Les récepteurs purinergiques P2Y ont un rôle modulateur de la sécrétion d'insuline et constituent une cible potentielle pour la recherche de nouveaux antidiabétiques. Dans le… (more)

Subjects/Keywords: Récepteurs purinergiques P2Y; Insulinosécretion; Diabète; Purinergic receptors p2y; Insulin secretion; Diabetes

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

APA (6th Edition):

Farret, A. (2010). Effets et mécanismes de l'activation des récepteurs purinergiques P2Y de la cellule beta pancréatique : Effects and mechanisms of activation of P2Y purinergic receptors of the pancreatic beta cell. (Doctoral Dissertation). Université Montpellier I. Retrieved from http://www.theses.fr/2010MON1T020

Chicago Manual of Style (16th Edition):

Farret, Anne. “Effets et mécanismes de l'activation des récepteurs purinergiques P2Y de la cellule beta pancréatique : Effects and mechanisms of activation of P2Y purinergic receptors of the pancreatic beta cell.” 2010. Doctoral Dissertation, Université Montpellier I. Accessed September 19, 2019. http://www.theses.fr/2010MON1T020.

MLA Handbook (7th Edition):

Farret, Anne. “Effets et mécanismes de l'activation des récepteurs purinergiques P2Y de la cellule beta pancréatique : Effects and mechanisms of activation of P2Y purinergic receptors of the pancreatic beta cell.” 2010. Web. 19 Sep 2019.

Vancouver:

Farret A. Effets et mécanismes de l'activation des récepteurs purinergiques P2Y de la cellule beta pancréatique : Effects and mechanisms of activation of P2Y purinergic receptors of the pancreatic beta cell. [Internet] [Doctoral dissertation]. Université Montpellier I; 2010. [cited 2019 Sep 19]. Available from: http://www.theses.fr/2010MON1T020.

Council of Science Editors:

Farret A. Effets et mécanismes de l'activation des récepteurs purinergiques P2Y de la cellule beta pancréatique : Effects and mechanisms of activation of P2Y purinergic receptors of the pancreatic beta cell. [Doctoral Dissertation]. Université Montpellier I; 2010. Available from: http://www.theses.fr/2010MON1T020


Virginia Tech

21. Fu, Zhuo. The anti-diabetic mechanisms by isoflavone genistein.

Degree: PhD, Human Nutrition, Foods, and Exercise, 2011, Virginia Tech

 Diabetes is growing public health problem in the United States. Both in Type 1 and Type 2 diabetes, the deterioration of glycemic control over time… (more)

Subjects/Keywords: apoptosis; proliferation; insulin secretion; β-cell; diabetes; genistein

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APA (6th Edition):

Fu, Z. (2011). The anti-diabetic mechanisms by isoflavone genistein. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/37816

Chicago Manual of Style (16th Edition):

Fu, Zhuo. “The anti-diabetic mechanisms by isoflavone genistein.” 2011. Doctoral Dissertation, Virginia Tech. Accessed September 19, 2019. http://hdl.handle.net/10919/37816.

MLA Handbook (7th Edition):

Fu, Zhuo. “The anti-diabetic mechanisms by isoflavone genistein.” 2011. Web. 19 Sep 2019.

Vancouver:

Fu Z. The anti-diabetic mechanisms by isoflavone genistein. [Internet] [Doctoral dissertation]. Virginia Tech; 2011. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/10919/37816.

Council of Science Editors:

Fu Z. The anti-diabetic mechanisms by isoflavone genistein. [Doctoral Dissertation]. Virginia Tech; 2011. Available from: http://hdl.handle.net/10919/37816


Vanderbilt University

22. Pound, Lynley Dayle. Characterization of islet genes implicated in human disease.

Degree: PhD, Molecular Physiology and Biophysics, 2011, Vanderbilt University

 Recent genome wide association (GWA) studies have linked single nucleotide polymorphisms (SNPs) in the G6PC2 gene with elevated fasting plasma glucose (FPG) and in the… (more)

Subjects/Keywords: fasting blood glucose; type 2 diabetes; insulin secretion; ZnT8; G6pc2

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

APA (6th Edition):

Pound, L. D. (2011). Characterization of islet genes implicated in human disease. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-08292011-155636/ ;

Chicago Manual of Style (16th Edition):

Pound, Lynley Dayle. “Characterization of islet genes implicated in human disease.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed September 19, 2019. http://etd.library.vanderbilt.edu/available/etd-08292011-155636/ ;.

MLA Handbook (7th Edition):

Pound, Lynley Dayle. “Characterization of islet genes implicated in human disease.” 2011. Web. 19 Sep 2019.

Vancouver:

Pound LD. Characterization of islet genes implicated in human disease. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2019 Sep 19]. Available from: http://etd.library.vanderbilt.edu/available/etd-08292011-155636/ ;.

Council of Science Editors:

Pound LD. Characterization of islet genes implicated in human disease. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://etd.library.vanderbilt.edu/available/etd-08292011-155636/ ;


Vanderbilt University

23. Ustione, Alessandro. Dopaminergic regulation of insulin secretion from the pancreatic islet.

Degree: PhD, Molecular Physiology and Biophysics, 2012, Vanderbilt University

Insulin secretion is the natural response to hyperglycemia, and it is crucial to maintain glucose homeostasis in healthy individuals. Impairment in this regulation eventually results… (more)

Subjects/Keywords: pancreatic islet; dopamine; dopamine receptor; dopamine transporter; diabetes; insulin secretion

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

APA (6th Edition):

Ustione, A. (2012). Dopaminergic regulation of insulin secretion from the pancreatic islet. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-11302012-115134/ ;

Chicago Manual of Style (16th Edition):

Ustione, Alessandro. “Dopaminergic regulation of insulin secretion from the pancreatic islet.” 2012. Doctoral Dissertation, Vanderbilt University. Accessed September 19, 2019. http://etd.library.vanderbilt.edu/available/etd-11302012-115134/ ;.

MLA Handbook (7th Edition):

Ustione, Alessandro. “Dopaminergic regulation of insulin secretion from the pancreatic islet.” 2012. Web. 19 Sep 2019.

Vancouver:

Ustione A. Dopaminergic regulation of insulin secretion from the pancreatic islet. [Internet] [Doctoral dissertation]. Vanderbilt University; 2012. [cited 2019 Sep 19]. Available from: http://etd.library.vanderbilt.edu/available/etd-11302012-115134/ ;.

Council of Science Editors:

Ustione A. Dopaminergic regulation of insulin secretion from the pancreatic islet. [Doctoral Dissertation]. Vanderbilt University; 2012. Available from: http://etd.library.vanderbilt.edu/available/etd-11302012-115134/ ;


University of Waterloo

24. Pillai, Renjitha. Mechanistic Role of ARNT/HIF-1β in the Regulation of Glucose-Stimulated Insulin Secretion.

Degree: 2014, University of Waterloo

 Loss of glucose-stimulated insulin secretion (GSIS) from the pancreatic beta-cells is one of the earliest detectable defects in the pathogenesis of type 2 diabetes. However,… (more)

Subjects/Keywords: ARNT/HIF-1β; type 2 diabetes; insulin secretion; glucose metabolism

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APA (6th Edition):

Pillai, R. (2014). Mechanistic Role of ARNT/HIF-1β in the Regulation of Glucose-Stimulated Insulin Secretion. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/8376

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):

Pillai, Renjitha. “Mechanistic Role of ARNT/HIF-1β in the Regulation of Glucose-Stimulated Insulin Secretion.” 2014. Thesis, University of Waterloo. Accessed September 19, 2019. http://hdl.handle.net/10012/8376.

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

MLA Handbook (7th Edition):

Pillai, Renjitha. “Mechanistic Role of ARNT/HIF-1β in the Regulation of Glucose-Stimulated Insulin Secretion.” 2014. Web. 19 Sep 2019.

Vancouver:

Pillai R. Mechanistic Role of ARNT/HIF-1β in the Regulation of Glucose-Stimulated Insulin Secretion. [Internet] [Thesis]. University of Waterloo; 2014. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/10012/8376.

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

Council of Science Editors:

Pillai R. Mechanistic Role of ARNT/HIF-1β in the Regulation of Glucose-Stimulated Insulin Secretion. [Thesis]. University of Waterloo; 2014. Available from: http://hdl.handle.net/10012/8376

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


University of California – San Francisco

25. Hennings, Thomas George. Mitochondrial Fission in Pancreatic Beta Cell Insulin Secretion.

Degree: Biomedical Sciences, 2018, University of California – San Francisco

Insulin-producing pancreatic beta cells are central regulators of blood glucose homeostasis. In a process termed glucose-stimulated insulin secretion (GSIS) beta cells utilize mitochondrial glucose metabolism… (more)

Subjects/Keywords: Biology; Beta cell; Diabetes; Endocrinology; Insulin secretion; Mitochondria; Pancreas

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APA (6th Edition):

Hennings, T. G. (2018). Mitochondrial Fission in Pancreatic Beta Cell Insulin Secretion. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/35n8q7vt

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):

Hennings, Thomas George. “Mitochondrial Fission in Pancreatic Beta Cell Insulin Secretion.” 2018. Thesis, University of California – San Francisco. Accessed September 19, 2019. http://www.escholarship.org/uc/item/35n8q7vt.

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

MLA Handbook (7th Edition):

Hennings, Thomas George. “Mitochondrial Fission in Pancreatic Beta Cell Insulin Secretion.” 2018. Web. 19 Sep 2019.

Vancouver:

Hennings TG. Mitochondrial Fission in Pancreatic Beta Cell Insulin Secretion. [Internet] [Thesis]. University of California – San Francisco; 2018. [cited 2019 Sep 19]. Available from: http://www.escholarship.org/uc/item/35n8q7vt.

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

Council of Science Editors:

Hennings TG. Mitochondrial Fission in Pancreatic Beta Cell Insulin Secretion. [Thesis]. University of California – San Francisco; 2018. Available from: http://www.escholarship.org/uc/item/35n8q7vt

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


University of New South Wales

26. Cheng, Kim. First phase insulin secretion.

Degree: Garvan Institute of Medical Research, 2012, University of New South Wales

 Type 2 diabetes (T2D) is a metabolic disorder characterised by the inability of β-cells to secrete enough insulin to maintain glucose homeostasis. Pancreatic β-cells secrete… (more)

Subjects/Keywords: Hypoxia inducible factor; Type 2 Diabetes; Insulin Secretion

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APA (6th Edition):

Cheng, K. (2012). First phase insulin secretion. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/52259 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10931/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Cheng, Kim. “First phase insulin secretion.” 2012. Doctoral Dissertation, University of New South Wales. Accessed September 19, 2019. http://handle.unsw.edu.au/1959.4/52259 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10931/SOURCE01?view=true.

MLA Handbook (7th Edition):

Cheng, Kim. “First phase insulin secretion.” 2012. Web. 19 Sep 2019.

Vancouver:

Cheng K. First phase insulin secretion. [Internet] [Doctoral dissertation]. University of New South Wales; 2012. [cited 2019 Sep 19]. Available from: http://handle.unsw.edu.au/1959.4/52259 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10931/SOURCE01?view=true.

Council of Science Editors:

Cheng K. First phase insulin secretion. [Doctoral Dissertation]. University of New South Wales; 2012. Available from: http://handle.unsw.edu.au/1959.4/52259 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10931/SOURCE01?view=true


Boston University

27. Alsabeeh, Nour. Role of mitochondrial dysfunction in the development of nutrient-induced hyperinsulinemia.

Degree: PhD, Physiology, 2018, Boston University

 Pancreatic beta cells sense fluctuations in circulating nutrients and adjust the rate of insulin secretion to maintain glucose homeostasis. Mitochondria integrate changes in nutrient flux… (more)

Subjects/Keywords: Physiology; Cyclophilin D; Diabetes; Insulin secretion; Islet; Mitochondria; Proton leak

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APA (6th Edition):

Alsabeeh, N. (2018). Role of mitochondrial dysfunction in the development of nutrient-induced hyperinsulinemia. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/29271

Chicago Manual of Style (16th Edition):

Alsabeeh, Nour. “Role of mitochondrial dysfunction in the development of nutrient-induced hyperinsulinemia.” 2018. Doctoral Dissertation, Boston University. Accessed September 19, 2019. http://hdl.handle.net/2144/29271.

MLA Handbook (7th Edition):

Alsabeeh, Nour. “Role of mitochondrial dysfunction in the development of nutrient-induced hyperinsulinemia.” 2018. Web. 19 Sep 2019.

Vancouver:

Alsabeeh N. Role of mitochondrial dysfunction in the development of nutrient-induced hyperinsulinemia. [Internet] [Doctoral dissertation]. Boston University; 2018. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/2144/29271.

Council of Science Editors:

Alsabeeh N. Role of mitochondrial dysfunction in the development of nutrient-induced hyperinsulinemia. [Doctoral Dissertation]. Boston University; 2018. Available from: http://hdl.handle.net/2144/29271


Brigham Young University

28. Rowley, Thomas John. The Effect of Cocoa Flavanols on β-Cell Mass and Function.

Degree: MS, 2017, Brigham Young University

 A hallmark of type 2 diabetes (T2D) is β-cell dysfunction and the eventual loss of functional β-cell mass. Therefore, mechanisms that improve or preserve β-cell… (more)

Subjects/Keywords: cocoa; β-cell; catechin; insulin secretion; mitochondrial respiration; Nrf2; Nutrition

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APA (6th Edition):

Rowley, T. J. (2017). The Effect of Cocoa Flavanols on β-Cell Mass and Function. (Masters Thesis). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7508&context=etd

Chicago Manual of Style (16th Edition):

Rowley, Thomas John. “The Effect of Cocoa Flavanols on β-Cell Mass and Function.” 2017. Masters Thesis, Brigham Young University. Accessed September 19, 2019. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7508&context=etd.

MLA Handbook (7th Edition):

Rowley, Thomas John. “The Effect of Cocoa Flavanols on β-Cell Mass and Function.” 2017. Web. 19 Sep 2019.

Vancouver:

Rowley TJ. The Effect of Cocoa Flavanols on β-Cell Mass and Function. [Internet] [Masters thesis]. Brigham Young University; 2017. [cited 2019 Sep 19]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7508&context=etd.

Council of Science Editors:

Rowley TJ. The Effect of Cocoa Flavanols on β-Cell Mass and Function. [Masters Thesis]. Brigham Young University; 2017. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7508&context=etd


Boston University

29. Erion, Karel Arnt. Nutrient regulation of insulin secretion: implications for hyperinsulinemia.

Degree: PhD, Medical Nutritional Sciences, 2016, Boston University

 Pancreatic beta-cells regulate blood glucose by secreting insulin in response to nutrients. The development of Type 2 Diabetes (T2D) is characterized by elevated insulin secretion(more)

Subjects/Keywords: Endocrinology; Beta-cell; Calcium; Diabetes; Fatty acid; Hyperinsulinemia; Insulin secretion

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

APA (6th Edition):

Erion, K. A. (2016). Nutrient regulation of insulin secretion: implications for hyperinsulinemia. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/16726

Chicago Manual of Style (16th Edition):

Erion, Karel Arnt. “Nutrient regulation of insulin secretion: implications for hyperinsulinemia.” 2016. Doctoral Dissertation, Boston University. Accessed September 19, 2019. http://hdl.handle.net/2144/16726.

MLA Handbook (7th Edition):

Erion, Karel Arnt. “Nutrient regulation of insulin secretion: implications for hyperinsulinemia.” 2016. Web. 19 Sep 2019.

Vancouver:

Erion KA. Nutrient regulation of insulin secretion: implications for hyperinsulinemia. [Internet] [Doctoral dissertation]. Boston University; 2016. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/2144/16726.

Council of Science Editors:

Erion KA. Nutrient regulation of insulin secretion: implications for hyperinsulinemia. [Doctoral Dissertation]. Boston University; 2016. Available from: http://hdl.handle.net/2144/16726


University of Michigan

30. Cipolla, Cynthia Marie. Development and Application of Analytical Techniques for Evaluating Function in Pancreatic Islets of Langerhans.

Degree: PhD, Chemistry, 2015, University of Michigan

 Type 1 diabetes is caused by autoimmune destruction of insulin-secreting beta-cells found in the islets of Langerhans of the pancreas. Severe cases can be treated… (more)

Subjects/Keywords: Bioanalytical chemistry; Microfluidics; Metabolomics; Insulin secretion; Oxidative stress; Chemistry; Science

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

APA (6th Edition):

Cipolla, C. M. (2015). Development and Application of Analytical Techniques for Evaluating Function in Pancreatic Islets of Langerhans. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/113374

Chicago Manual of Style (16th Edition):

Cipolla, Cynthia Marie. “Development and Application of Analytical Techniques for Evaluating Function in Pancreatic Islets of Langerhans.” 2015. Doctoral Dissertation, University of Michigan. Accessed September 19, 2019. http://hdl.handle.net/2027.42/113374.

MLA Handbook (7th Edition):

Cipolla, Cynthia Marie. “Development and Application of Analytical Techniques for Evaluating Function in Pancreatic Islets of Langerhans.” 2015. Web. 19 Sep 2019.

Vancouver:

Cipolla CM. Development and Application of Analytical Techniques for Evaluating Function in Pancreatic Islets of Langerhans. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/2027.42/113374.

Council of Science Editors:

Cipolla CM. Development and Application of Analytical Techniques for Evaluating Function in Pancreatic Islets of Langerhans. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/113374

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