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You searched for subject:(insulin receptor). Showing records 1 – 30 of 159 total matches.

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University of Canterbury

1. Subramanian, Kannan. Kinetics of insulin - insulin receptor interaction using a surface plasmon resonance (SPR).

Degree: Chemical and Process Engineering, 2014, University of Canterbury

 Type 2 diabetes or adult onset diabetes, has been a global epidemic for the past two decades, and the number of new cases accelerates every… (more)

Subjects/Keywords: insulin; insulin-receptor; kinetics; surface plasmon resonance

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APA (6th Edition):

Subramanian, K. (2014). Kinetics of insulin - insulin receptor interaction using a surface plasmon resonance (SPR). (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/9327

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):

Subramanian, Kannan. “Kinetics of insulin - insulin receptor interaction using a surface plasmon resonance (SPR).” 2014. Thesis, University of Canterbury. Accessed April 19, 2019. http://hdl.handle.net/10092/9327.

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

MLA Handbook (7th Edition):

Subramanian, Kannan. “Kinetics of insulin - insulin receptor interaction using a surface plasmon resonance (SPR).” 2014. Web. 19 Apr 2019.

Vancouver:

Subramanian K. Kinetics of insulin - insulin receptor interaction using a surface plasmon resonance (SPR). [Internet] [Thesis]. University of Canterbury; 2014. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/10092/9327.

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

Council of Science Editors:

Subramanian K. Kinetics of insulin - insulin receptor interaction using a surface plasmon resonance (SPR). [Thesis]. University of Canterbury; 2014. Available from: http://hdl.handle.net/10092/9327

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


University of Adelaide

2. Bonython, Eric Richard. Investigation of insulin-like receptor systems.

Degree: 2005, University of Adelaide

 The insulin and insulin-like growth factor receptor (IR and IGF-lR respectively) networks are ancient and fundamental systems that control growth and metabolism in multicellular organisms.… (more)

Subjects/Keywords: insulin; receptor

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APA (6th Edition):

Bonython, E. R. (2005). Investigation of insulin-like receptor systems. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/59217

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):

Bonython, Eric Richard. “Investigation of insulin-like receptor systems.” 2005. Thesis, University of Adelaide. Accessed April 19, 2019. http://hdl.handle.net/2440/59217.

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

MLA Handbook (7th Edition):

Bonython, Eric Richard. “Investigation of insulin-like receptor systems.” 2005. Web. 19 Apr 2019.

Vancouver:

Bonython ER. Investigation of insulin-like receptor systems. [Internet] [Thesis]. University of Adelaide; 2005. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/2440/59217.

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

Council of Science Editors:

Bonython ER. Investigation of insulin-like receptor systems. [Thesis]. University of Adelaide; 2005. Available from: http://hdl.handle.net/2440/59217

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


University of Adelaide

3. Li, Liang. Role of insulin receptor isoform A in breast cancer.

Degree: 2017, University of Adelaide

Insulin like growth factor II (IGF-II) binds to Insulin Receptor isoform A (IR-A) to sustain cell growth and proliferation. This autocrine loop exists in many… (more)

Subjects/Keywords: Insulin receptor; cancer; IGF-II

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APA (6th Edition):

Li, L. (2017). Role of insulin receptor isoform A in breast cancer. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/113111

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):

Li, Liang. “Role of insulin receptor isoform A in breast cancer.” 2017. Thesis, University of Adelaide. Accessed April 19, 2019. http://hdl.handle.net/2440/113111.

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

MLA Handbook (7th Edition):

Li, Liang. “Role of insulin receptor isoform A in breast cancer.” 2017. Web. 19 Apr 2019.

Vancouver:

Li L. Role of insulin receptor isoform A in breast cancer. [Internet] [Thesis]. University of Adelaide; 2017. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/2440/113111.

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

Council of Science Editors:

Li L. Role of insulin receptor isoform A in breast cancer. [Thesis]. University of Adelaide; 2017. Available from: http://hdl.handle.net/2440/113111

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


Case Western Reserve University

4. Tao, Jia-Lin. The Molecular Mechanisms Underlying Ligand Specificity of the Insulin and IGF-I Receptors.

Degree: PhD, Nutrition, 2010, Case Western Reserve University

 The insulin receptor (IR) and insulin-like growth factor 1 receptor (IGFR) are membrane bound receptors belonging to the IR superfamily. IR, stimulated by insulin, conducts… (more)

Subjects/Keywords: Biochemistry; insulin; IGF; receptor; IGFBP; diabetes; cancer

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APA (6th Edition):

Tao, J. (2010). The Molecular Mechanisms Underlying Ligand Specificity of the Insulin and IGF-I Receptors. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1278613018

Chicago Manual of Style (16th Edition):

Tao, Jia-Lin. “The Molecular Mechanisms Underlying Ligand Specificity of the Insulin and IGF-I Receptors.” 2010. Doctoral Dissertation, Case Western Reserve University. Accessed April 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1278613018.

MLA Handbook (7th Edition):

Tao, Jia-Lin. “The Molecular Mechanisms Underlying Ligand Specificity of the Insulin and IGF-I Receptors.” 2010. Web. 19 Apr 2019.

Vancouver:

Tao J. The Molecular Mechanisms Underlying Ligand Specificity of the Insulin and IGF-I Receptors. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2010. [cited 2019 Apr 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1278613018.

Council of Science Editors:

Tao J. The Molecular Mechanisms Underlying Ligand Specificity of the Insulin and IGF-I Receptors. [Doctoral Dissertation]. Case Western Reserve University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1278613018


Case Western Reserve University

5. Sun, Zheng. IMIDAZOLINE RECEPTORS IN INSULIN SIGNALING AND METABOLIC REGULATION.

Degree: PhD, Nutrition, 2007, Case Western Reserve University

 The I1-imidazoline receptor is a novel target of drug development for hypertension and insulin resistance. This thesis focused on the molecular basis for I1-imidazoline binding… (more)

Subjects/Keywords: imidazoline receptor; IRAS; insulin resistance; moxonidine

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APA (6th Edition):

Sun, Z. (2007). IMIDAZOLINE RECEPTORS IN INSULIN SIGNALING AND METABOLIC REGULATION. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1157694260

Chicago Manual of Style (16th Edition):

Sun, Zheng. “IMIDAZOLINE RECEPTORS IN INSULIN SIGNALING AND METABOLIC REGULATION.” 2007. Doctoral Dissertation, Case Western Reserve University. Accessed April 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1157694260.

MLA Handbook (7th Edition):

Sun, Zheng. “IMIDAZOLINE RECEPTORS IN INSULIN SIGNALING AND METABOLIC REGULATION.” 2007. Web. 19 Apr 2019.

Vancouver:

Sun Z. IMIDAZOLINE RECEPTORS IN INSULIN SIGNALING AND METABOLIC REGULATION. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2007. [cited 2019 Apr 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1157694260.

Council of Science Editors:

Sun Z. IMIDAZOLINE RECEPTORS IN INSULIN SIGNALING AND METABOLIC REGULATION. [Doctoral Dissertation]. Case Western Reserve University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1157694260


University of Minnesota

6. Fagan, Dedra Hannah. Examination of molecular changes in acquired tamoxifen resistance and subsequent response to anti-IGF1R therapy.

Degree: PhD, 2012, University of Minnesota

 The type-I insulin like growth factor (IGF1R) contributes to the proliferation, survival, and metastasis of breast cancer cells. Disruption of IGF1R signaling alone or in… (more)

Subjects/Keywords: Endocrine resistance; IGF1R; Insulin receptor; Pharmacology

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APA (6th Edition):

Fagan, D. H. (2012). Examination of molecular changes in acquired tamoxifen resistance and subsequent response to anti-IGF1R therapy. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/131512

Chicago Manual of Style (16th Edition):

Fagan, Dedra Hannah. “Examination of molecular changes in acquired tamoxifen resistance and subsequent response to anti-IGF1R therapy.” 2012. Doctoral Dissertation, University of Minnesota. Accessed April 19, 2019. http://purl.umn.edu/131512.

MLA Handbook (7th Edition):

Fagan, Dedra Hannah. “Examination of molecular changes in acquired tamoxifen resistance and subsequent response to anti-IGF1R therapy.” 2012. Web. 19 Apr 2019.

Vancouver:

Fagan DH. Examination of molecular changes in acquired tamoxifen resistance and subsequent response to anti-IGF1R therapy. [Internet] [Doctoral dissertation]. University of Minnesota; 2012. [cited 2019 Apr 19]. Available from: http://purl.umn.edu/131512.

Council of Science Editors:

Fagan DH. Examination of molecular changes in acquired tamoxifen resistance and subsequent response to anti-IGF1R therapy. [Doctoral Dissertation]. University of Minnesota; 2012. Available from: http://purl.umn.edu/131512


University of Iowa

7. Starks, Rachel Diaz. Molecular basis of insulin resistance in Bardet Biedl syndrome.

Degree: PhD, Molecular and Cell Biology, 2015, University of Iowa

  Bardet Biedl Syndrome (BBS) displays heterogeneity in the genes involved and clinical features. Mutations in 19 genes have been associated with BBS. Eight BBS… (more)

Subjects/Keywords: BBSome; BBS proteins; glucose homeostasis; insulin receptor; insulin resistance; Cell Biology

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APA (6th Edition):

Starks, R. D. (2015). Molecular basis of insulin resistance in Bardet Biedl syndrome. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/5641

Chicago Manual of Style (16th Edition):

Starks, Rachel Diaz. “Molecular basis of insulin resistance in Bardet Biedl syndrome.” 2015. Doctoral Dissertation, University of Iowa. Accessed April 19, 2019. https://ir.uiowa.edu/etd/5641.

MLA Handbook (7th Edition):

Starks, Rachel Diaz. “Molecular basis of insulin resistance in Bardet Biedl syndrome.” 2015. Web. 19 Apr 2019.

Vancouver:

Starks RD. Molecular basis of insulin resistance in Bardet Biedl syndrome. [Internet] [Doctoral dissertation]. University of Iowa; 2015. [cited 2019 Apr 19]. Available from: https://ir.uiowa.edu/etd/5641.

Council of Science Editors:

Starks RD. Molecular basis of insulin resistance in Bardet Biedl syndrome. [Doctoral Dissertation]. University of Iowa; 2015. Available from: https://ir.uiowa.edu/etd/5641


University of Illinois – Urbana-Champaign

8. Cervantes, David. Modulation of mitogenic signaling and growth by sympathetic adrenergic regulation.

Degree: PhD, 0325, 2012, University of Illinois – Urbana-Champaign

 Heart disease and diabetes mellitus are growing epidemics, consistently ranking within the top ten causes of death in the United States. Both diseases are associated… (more)

Subjects/Keywords: adrenergic receptor; insulin receptor; extracellular signal-regulated kinase (ERK); heart; arrestin

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APA (6th Edition):

Cervantes, D. (2012). Modulation of mitogenic signaling and growth by sympathetic adrenergic regulation. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/29837

Chicago Manual of Style (16th Edition):

Cervantes, David. “Modulation of mitogenic signaling and growth by sympathetic adrenergic regulation.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed April 19, 2019. http://hdl.handle.net/2142/29837.

MLA Handbook (7th Edition):

Cervantes, David. “Modulation of mitogenic signaling and growth by sympathetic adrenergic regulation.” 2012. Web. 19 Apr 2019.

Vancouver:

Cervantes D. Modulation of mitogenic signaling and growth by sympathetic adrenergic regulation. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/2142/29837.

Council of Science Editors:

Cervantes D. Modulation of mitogenic signaling and growth by sympathetic adrenergic regulation. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/29837


Texas A&M University

9. Lu, Hsiao Ling. Vitellogenin Receptor and Neuropeptide Receptors Involved in Reproduction of the Red Imported Fire Ant (Solenopsis invicta Buren).

Degree: 2012, Texas A&M University

 Social insects have complex forms of social organization. Molecular mechanisms involved in the regulation of their reproduction are not fully understood. This dissertation investigated the… (more)

Subjects/Keywords: Fire ants; vitellogenin receptor; short neuropeptide F receptor; insulin receptor; queen reproduction

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APA (6th Edition):

Lu, H. L. (2012). Vitellogenin Receptor and Neuropeptide Receptors Involved in Reproduction of the Red Imported Fire Ant (Solenopsis invicta Buren). (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10218

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):

Lu, Hsiao Ling. “Vitellogenin Receptor and Neuropeptide Receptors Involved in Reproduction of the Red Imported Fire Ant (Solenopsis invicta Buren).” 2012. Thesis, Texas A&M University. Accessed April 19, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10218.

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

MLA Handbook (7th Edition):

Lu, Hsiao Ling. “Vitellogenin Receptor and Neuropeptide Receptors Involved in Reproduction of the Red Imported Fire Ant (Solenopsis invicta Buren).” 2012. Web. 19 Apr 2019.

Vancouver:

Lu HL. Vitellogenin Receptor and Neuropeptide Receptors Involved in Reproduction of the Red Imported Fire Ant (Solenopsis invicta Buren). [Internet] [Thesis]. Texas A&M University; 2012. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10218.

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

Council of Science Editors:

Lu HL. Vitellogenin Receptor and Neuropeptide Receptors Involved in Reproduction of the Red Imported Fire Ant (Solenopsis invicta Buren). [Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10218

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


Univerzitet u Beogradu

10. Prodanović, Radiša, 1981-. Insulinska rezistencija kod krava Holštajn rase tokom perioda zasušenja i rane laktacije.

Degree: Fakultet veterinarske medicine, 2015, Univerzitet u Beogradu

Veterinarska medicina - Bolesti papkara / Veterinary Medicine - Ruminants and Swine Diseases

Cilj istraživanja u okviru ove disertacije je bio da se ispita da… (more)

Subjects/Keywords: high-yielding dairy cows; body condition; insulin resistance; glucose tolerance test; insulin receptor; GLUT 4

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APA (6th Edition):

Prodanović, Radiša, 1. (2015). Insulinska rezistencija kod krava Holštajn rase tokom perioda zasušenja i rane laktacije. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:8045/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):

Prodanović, Radiša, 1981-. “Insulinska rezistencija kod krava Holštajn rase tokom perioda zasušenja i rane laktacije.” 2015. Thesis, Univerzitet u Beogradu. Accessed April 19, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:8045/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):

Prodanović, Radiša, 1981-. “Insulinska rezistencija kod krava Holštajn rase tokom perioda zasušenja i rane laktacije.” 2015. Web. 19 Apr 2019.

Vancouver:

Prodanović, Radiša 1. Insulinska rezistencija kod krava Holštajn rase tokom perioda zasušenja i rane laktacije. [Internet] [Thesis]. Univerzitet u Beogradu; 2015. [cited 2019 Apr 19]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:8045/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:

Prodanović, Radiša 1. Insulinska rezistencija kod krava Holštajn rase tokom perioda zasušenja i rane laktacije. [Thesis]. Univerzitet u Beogradu; 2015. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:8045/bdef:Content/get

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


University of Arizona

11. Ananthakrishnan, Kameswari. Improved β-Cell Targeting and Therapeutics Using Multivalent Glucagon-Like Peptide-1 (GLP-1) Linked to the α2AR Antagonist Yohimbine (YHB): Evaluating the Binding, Selectivity and Signaling .

Degree: 2016, University of Arizona

 Diabetes Mellitus (DM) is a metabolic disorder in which the body fails to achieve glucose homeostasis, due to either insulin resistance or reduced insulin secretion… (more)

Subjects/Keywords: GLP-1; Insulin secretion; Multivalency; Receptor targeting; β-cell imaging; Adrenergic receptor

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APA (6th Edition):

Ananthakrishnan, K. (2016). Improved β-Cell Targeting and Therapeutics Using Multivalent Glucagon-Like Peptide-1 (GLP-1) Linked to the α2AR Antagonist Yohimbine (YHB): Evaluating the Binding, Selectivity and Signaling . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/623004

Chicago Manual of Style (16th Edition):

Ananthakrishnan, Kameswari. “Improved β-Cell Targeting and Therapeutics Using Multivalent Glucagon-Like Peptide-1 (GLP-1) Linked to the α2AR Antagonist Yohimbine (YHB): Evaluating the Binding, Selectivity and Signaling .” 2016. Doctoral Dissertation, University of Arizona. Accessed April 19, 2019. http://hdl.handle.net/10150/623004.

MLA Handbook (7th Edition):

Ananthakrishnan, Kameswari. “Improved β-Cell Targeting and Therapeutics Using Multivalent Glucagon-Like Peptide-1 (GLP-1) Linked to the α2AR Antagonist Yohimbine (YHB): Evaluating the Binding, Selectivity and Signaling .” 2016. Web. 19 Apr 2019.

Vancouver:

Ananthakrishnan K. Improved β-Cell Targeting and Therapeutics Using Multivalent Glucagon-Like Peptide-1 (GLP-1) Linked to the α2AR Antagonist Yohimbine (YHB): Evaluating the Binding, Selectivity and Signaling . [Internet] [Doctoral dissertation]. University of Arizona; 2016. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/10150/623004.

Council of Science Editors:

Ananthakrishnan K. Improved β-Cell Targeting and Therapeutics Using Multivalent Glucagon-Like Peptide-1 (GLP-1) Linked to the α2AR Antagonist Yohimbine (YHB): Evaluating the Binding, Selectivity and Signaling . [Doctoral Dissertation]. University of Arizona; 2016. Available from: http://hdl.handle.net/10150/623004


University of Utah

12. Komanetsky, Susan M. Characterization of retinol binding protein receptor 2, a putative retinol transporter and serum retinol binding protein receptor.

Degree: MS, Nutrition, 2013, University of Utah

 min A (retinol) is essential for life; however, little is known about how it istransported into cells. Ninety-five percent of retinol found in blood is… (more)

Subjects/Keywords: Insulin resistance; RBP4; RBP4 receptor; Retinol; Retinol homeostasis; Retinol transport

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APA (6th Edition):

Komanetsky, S. M. (2013). Characterization of retinol binding protein receptor 2, a putative retinol transporter and serum retinol binding protein receptor. (Masters Thesis). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2302/rec/432

Chicago Manual of Style (16th Edition):

Komanetsky, Susan M. “Characterization of retinol binding protein receptor 2, a putative retinol transporter and serum retinol binding protein receptor.” 2013. Masters Thesis, University of Utah. Accessed April 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2302/rec/432.

MLA Handbook (7th Edition):

Komanetsky, Susan M. “Characterization of retinol binding protein receptor 2, a putative retinol transporter and serum retinol binding protein receptor.” 2013. Web. 19 Apr 2019.

Vancouver:

Komanetsky SM. Characterization of retinol binding protein receptor 2, a putative retinol transporter and serum retinol binding protein receptor. [Internet] [Masters thesis]. University of Utah; 2013. [cited 2019 Apr 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2302/rec/432.

Council of Science Editors:

Komanetsky SM. Characterization of retinol binding protein receptor 2, a putative retinol transporter and serum retinol binding protein receptor. [Masters Thesis]. University of Utah; 2013. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2302/rec/432


University of Pretoria

13. Hughes, Stephen Bernard. Development of real-time reverse transcription polymerase chain reaction assays to quantify insulin-like growth factor-1 receptor and insulin receptor expression in equine tissue.

Degree: Production Animal Studies, 2012, University of Pretoria

 has been significant progress in the development of new technologies and methodologies to characterize gene expression. The fluorescent-based real-time reverse transcription (RT) polymerase chain reaction… (more)

Subjects/Keywords: Insulin receptor; UCTD; Equine tissue; Transcription polymerase; Tyrosine protein kinases

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APA (6th Edition):

Hughes, S. B. (2012). Development of real-time reverse transcription polymerase chain reaction assays to quantify insulin-like growth factor-1 receptor and insulin receptor expression in equine tissue. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/31135

Chicago Manual of Style (16th Edition):

Hughes, Stephen Bernard. “Development of real-time reverse transcription polymerase chain reaction assays to quantify insulin-like growth factor-1 receptor and insulin receptor expression in equine tissue.” 2012. Masters Thesis, University of Pretoria. Accessed April 19, 2019. http://hdl.handle.net/2263/31135.

MLA Handbook (7th Edition):

Hughes, Stephen Bernard. “Development of real-time reverse transcription polymerase chain reaction assays to quantify insulin-like growth factor-1 receptor and insulin receptor expression in equine tissue.” 2012. Web. 19 Apr 2019.

Vancouver:

Hughes SB. Development of real-time reverse transcription polymerase chain reaction assays to quantify insulin-like growth factor-1 receptor and insulin receptor expression in equine tissue. [Internet] [Masters thesis]. University of Pretoria; 2012. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/2263/31135.

Council of Science Editors:

Hughes SB. Development of real-time reverse transcription polymerase chain reaction assays to quantify insulin-like growth factor-1 receptor and insulin receptor expression in equine tissue. [Masters Thesis]. University of Pretoria; 2012. Available from: http://hdl.handle.net/2263/31135


AUT University

14. Jain, Reema. When too much sun is never enough: association of the VDR gene polymorphisms with insulin resistance .

Degree: 2010, AUT University

 The metabolism of vitamin D commences with exposure of the skin to sunlight. The growing recognition of its role in insulin resistance, autoimmune disorders, infections,… (more)

Subjects/Keywords: Vitamin D receptor; Polymorphisms; Haplotype; Association; Insulin resistance; RFLP-PCR

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APA (6th Edition):

Jain, R. (2010). When too much sun is never enough: association of the VDR gene polymorphisms with insulin resistance . (Thesis). AUT University. Retrieved from http://hdl.handle.net/10292/990

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):

Jain, Reema. “When too much sun is never enough: association of the VDR gene polymorphisms with insulin resistance .” 2010. Thesis, AUT University. Accessed April 19, 2019. http://hdl.handle.net/10292/990.

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

MLA Handbook (7th Edition):

Jain, Reema. “When too much sun is never enough: association of the VDR gene polymorphisms with insulin resistance .” 2010. Web. 19 Apr 2019.

Vancouver:

Jain R. When too much sun is never enough: association of the VDR gene polymorphisms with insulin resistance . [Internet] [Thesis]. AUT University; 2010. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/10292/990.

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

Council of Science Editors:

Jain R. When too much sun is never enough: association of the VDR gene polymorphisms with insulin resistance . [Thesis]. AUT University; 2010. Available from: http://hdl.handle.net/10292/990

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


University of Pretoria

15. Hughes, Stephen Bernard. Development of real-time reverse transcription polymerase chain reaction assays to quantify insulin-like growth factor-1 receptor and insulin receptor expression in equine tissue .

Degree: 2012, University of Pretoria

 has been significant progress in the development of new technologies and methodologies to characterize gene expression. The fluorescent-based real-time reverse transcription (RT) polymerase chain reaction… (more)

Subjects/Keywords: Insulin receptor; UCTD; Equine tissue; Transcription polymerase; Tyrosine protein kinases

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APA (6th Edition):

Hughes, S. B. (2012). Development of real-time reverse transcription polymerase chain reaction assays to quantify insulin-like growth factor-1 receptor and insulin receptor expression in equine tissue . (Masters Thesis). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-08082012-144801/

Chicago Manual of Style (16th Edition):

Hughes, Stephen Bernard. “Development of real-time reverse transcription polymerase chain reaction assays to quantify insulin-like growth factor-1 receptor and insulin receptor expression in equine tissue .” 2012. Masters Thesis, University of Pretoria. Accessed April 19, 2019. http://upetd.up.ac.za/thesis/available/etd-08082012-144801/.

MLA Handbook (7th Edition):

Hughes, Stephen Bernard. “Development of real-time reverse transcription polymerase chain reaction assays to quantify insulin-like growth factor-1 receptor and insulin receptor expression in equine tissue .” 2012. Web. 19 Apr 2019.

Vancouver:

Hughes SB. Development of real-time reverse transcription polymerase chain reaction assays to quantify insulin-like growth factor-1 receptor and insulin receptor expression in equine tissue . [Internet] [Masters thesis]. University of Pretoria; 2012. [cited 2019 Apr 19]. Available from: http://upetd.up.ac.za/thesis/available/etd-08082012-144801/.

Council of Science Editors:

Hughes SB. Development of real-time reverse transcription polymerase chain reaction assays to quantify insulin-like growth factor-1 receptor and insulin receptor expression in equine tissue . [Masters Thesis]. University of Pretoria; 2012. Available from: http://upetd.up.ac.za/thesis/available/etd-08082012-144801/

16. Landis, Justine M. Mechanistic Analysis of Differential Signal Transduction Mediated by the Insulin Receptor Substrate Proteins IRS-1 and IRS-2: A Dissertation.

Degree: Cancer Biology, Molecular, Cell and Cancer Biology Department, 2014, U of Massachusetts : Med

  The Insulin Receptor Substrate (IRS) proteins IRS-1 and IRS-2 are cytoplasmic adaptor proteins that organize and propagate intracellular signaling downstream of specific growth factor… (more)

Subjects/Keywords: Signal Transduction; Insulin Receptor Substrate Proteins; Biochemistry; Cancer Biology

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APA (6th Edition):

Landis, J. M. (2014). Mechanistic Analysis of Differential Signal Transduction Mediated by the Insulin Receptor Substrate Proteins IRS-1 and IRS-2: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/735

Chicago Manual of Style (16th Edition):

Landis, Justine M. “Mechanistic Analysis of Differential Signal Transduction Mediated by the Insulin Receptor Substrate Proteins IRS-1 and IRS-2: A Dissertation.” 2014. Doctoral Dissertation, U of Massachusetts : Med. Accessed April 19, 2019. http://escholarship.umassmed.edu/gsbs_diss/735.

MLA Handbook (7th Edition):

Landis, Justine M. “Mechanistic Analysis of Differential Signal Transduction Mediated by the Insulin Receptor Substrate Proteins IRS-1 and IRS-2: A Dissertation.” 2014. Web. 19 Apr 2019.

Vancouver:

Landis JM. Mechanistic Analysis of Differential Signal Transduction Mediated by the Insulin Receptor Substrate Proteins IRS-1 and IRS-2: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2014. [cited 2019 Apr 19]. Available from: http://escholarship.umassmed.edu/gsbs_diss/735.

Council of Science Editors:

Landis JM. Mechanistic Analysis of Differential Signal Transduction Mediated by the Insulin Receptor Substrate Proteins IRS-1 and IRS-2: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2014. Available from: http://escholarship.umassmed.edu/gsbs_diss/735


University of Toronto

17. Bansal, Pritpal. Insulin-induced Suppression of A-type GABA Receptor Signaling in the INS-1 Pancreatic β-cell Line.

Degree: 2010, University of Toronto

GABA and GABA type A receptor (GABAAR) are expressed in pancreatic β-cells and comprise an autocrine signaling system. How the GABA-GABAAR system is regulated is… (more)

Subjects/Keywords: GABA; Insulin; Beta-cell; Autocrine; GABA receptor; Islet; Electrophysiology; 0719

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APA (6th Edition):

Bansal, P. (2010). Insulin-induced Suppression of A-type GABA Receptor Signaling in the INS-1 Pancreatic β-cell Line. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25419

Chicago Manual of Style (16th Edition):

Bansal, Pritpal. “Insulin-induced Suppression of A-type GABA Receptor Signaling in the INS-1 Pancreatic β-cell Line.” 2010. Masters Thesis, University of Toronto. Accessed April 19, 2019. http://hdl.handle.net/1807/25419.

MLA Handbook (7th Edition):

Bansal, Pritpal. “Insulin-induced Suppression of A-type GABA Receptor Signaling in the INS-1 Pancreatic β-cell Line.” 2010. Web. 19 Apr 2019.

Vancouver:

Bansal P. Insulin-induced Suppression of A-type GABA Receptor Signaling in the INS-1 Pancreatic β-cell Line. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/1807/25419.

Council of Science Editors:

Bansal P. Insulin-induced Suppression of A-type GABA Receptor Signaling in the INS-1 Pancreatic β-cell Line. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25419


University of Southern California

18. Mangahas, Ana Marie E. The possible aberrant function of MBNL1 with insulin receptor (IR-B) mRNA in myotonic dystrophy type I.

Degree: MS, Biochemistry & Molecular Biology, 2007, University of Southern California

 Myotonic Dystrophy (DM) a multi-systemic disorder, is the most common adult muscular dystrophy form. Among the pathological manifestations observed in the skeletal musculature include non-muscle… (more)

Subjects/Keywords: Myotonic Dystrophy; insulin receptor

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APA (6th Edition):

Mangahas, A. M. E. (2007). The possible aberrant function of MBNL1 with insulin receptor (IR-B) mRNA in myotonic dystrophy type I. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/156892/rec/7102

Chicago Manual of Style (16th Edition):

Mangahas, Ana Marie E. “The possible aberrant function of MBNL1 with insulin receptor (IR-B) mRNA in myotonic dystrophy type I.” 2007. Masters Thesis, University of Southern California. Accessed April 19, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/156892/rec/7102.

MLA Handbook (7th Edition):

Mangahas, Ana Marie E. “The possible aberrant function of MBNL1 with insulin receptor (IR-B) mRNA in myotonic dystrophy type I.” 2007. Web. 19 Apr 2019.

Vancouver:

Mangahas AME. The possible aberrant function of MBNL1 with insulin receptor (IR-B) mRNA in myotonic dystrophy type I. [Internet] [Masters thesis]. University of Southern California; 2007. [cited 2019 Apr 19]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/156892/rec/7102.

Council of Science Editors:

Mangahas AME. The possible aberrant function of MBNL1 with insulin receptor (IR-B) mRNA in myotonic dystrophy type I. [Masters Thesis]. University of Southern California; 2007. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/156892/rec/7102


Harvard University

19. Green, Delbert Andre. Developmental and Genetic Mechanisms of Ovariole Number Evolution in Drosophila.

Degree: PhD, Biology, Molecular and Cellular, 2014, Harvard University

 The goal of the "Quantitative Trait Gene" (QTG) program is to identify genes and mutations that underlie natural phenotypic variation. My goal with this work… (more)

Subjects/Keywords: Biology; convergent evolution; Drosophila; Insulin Receptor; ovariole; plasticity

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APA (6th Edition):

Green, D. A. (2014). Developmental and Genetic Mechanisms of Ovariole Number Evolution in Drosophila. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274190

Chicago Manual of Style (16th Edition):

Green, Delbert Andre. “Developmental and Genetic Mechanisms of Ovariole Number Evolution in Drosophila.” 2014. Doctoral Dissertation, Harvard University. Accessed April 19, 2019. http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274190.

MLA Handbook (7th Edition):

Green, Delbert Andre. “Developmental and Genetic Mechanisms of Ovariole Number Evolution in Drosophila.” 2014. Web. 19 Apr 2019.

Vancouver:

Green DA. Developmental and Genetic Mechanisms of Ovariole Number Evolution in Drosophila. [Internet] [Doctoral dissertation]. Harvard University; 2014. [cited 2019 Apr 19]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274190.

Council of Science Editors:

Green DA. Developmental and Genetic Mechanisms of Ovariole Number Evolution in Drosophila. [Doctoral Dissertation]. Harvard University; 2014. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274190


Vanderbilt University

20. 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 (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 April 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 Apr 2019.

Vancouver:

Ustione A. Dopaminergic regulation of insulin secretion from the pancreatic islet. [Internet] [Doctoral dissertation]. Vanderbilt University; 2012. [cited 2019 Apr 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 New South Wales

21. Pedersen , David. The role of protein kinase C ε in insulin receptor trafficking and insulin action.

Degree: Clinical School - St Vincent's Hospital, 2012, University of New South Wales

 The development of type 2 diabetes is reaching epidemic proportions and identifying ways to modulate insulin levels in order to maintain euglycaemia is important in… (more)

Subjects/Keywords: Insulin Receptor; Protein Kinase C epsilon; Ceacam1; Trafficking; Signalling

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APA (6th Edition):

Pedersen , D. (2012). The role of protein kinase C ε in insulin receptor trafficking and insulin action. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/51788 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10455/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Pedersen , David. “The role of protein kinase C ε in insulin receptor trafficking and insulin action.” 2012. Doctoral Dissertation, University of New South Wales. Accessed April 19, 2019. http://handle.unsw.edu.au/1959.4/51788 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10455/SOURCE02?view=true.

MLA Handbook (7th Edition):

Pedersen , David. “The role of protein kinase C ε in insulin receptor trafficking and insulin action.” 2012. Web. 19 Apr 2019.

Vancouver:

Pedersen D. The role of protein kinase C ε in insulin receptor trafficking and insulin action. [Internet] [Doctoral dissertation]. University of New South Wales; 2012. [cited 2019 Apr 19]. Available from: http://handle.unsw.edu.au/1959.4/51788 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10455/SOURCE02?view=true.

Council of Science Editors:

Pedersen D. The role of protein kinase C ε in insulin receptor trafficking and insulin action. [Doctoral Dissertation]. University of New South Wales; 2012. Available from: http://handle.unsw.edu.au/1959.4/51788 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10455/SOURCE02?view=true


Universiteit Utrecht

22. Wilms, A.T. Protein expression of insuline-like growth factor I and II, growth hormone and growth hormone receptor in canine cortisol-producing adrenocortical tumors.

Degree: 2012, Universiteit Utrecht

 Cushing’s syndrome is an important endocrinological disorder in dogs. In 15-20% of the cases it is caused by excessive secretion of glucocorticoids by an adrenocortical… (more)

Subjects/Keywords: Cushing's syndrome; adrenocortical tumor; cortisol-producing adrenocortical ademonas; cortisol-producing adrenocortical carcinomas; growth hormone; growth hormone receptor; insulin-like growth factor I receptor; insulin-like growth factor II receptor

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APA (6th Edition):

Wilms, A. T. (2012). Protein expression of insuline-like growth factor I and II, growth hormone and growth hormone receptor in canine cortisol-producing adrenocortical tumors. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/289411

Chicago Manual of Style (16th Edition):

Wilms, A T. “Protein expression of insuline-like growth factor I and II, growth hormone and growth hormone receptor in canine cortisol-producing adrenocortical tumors.” 2012. Doctoral Dissertation, Universiteit Utrecht. Accessed April 19, 2019. http://dspace.library.uu.nl:8080/handle/1874/289411.

MLA Handbook (7th Edition):

Wilms, A T. “Protein expression of insuline-like growth factor I and II, growth hormone and growth hormone receptor in canine cortisol-producing adrenocortical tumors.” 2012. Web. 19 Apr 2019.

Vancouver:

Wilms AT. Protein expression of insuline-like growth factor I and II, growth hormone and growth hormone receptor in canine cortisol-producing adrenocortical tumors. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2012. [cited 2019 Apr 19]. Available from: http://dspace.library.uu.nl:8080/handle/1874/289411.

Council of Science Editors:

Wilms AT. Protein expression of insuline-like growth factor I and II, growth hormone and growth hormone receptor in canine cortisol-producing adrenocortical tumors. [Doctoral Dissertation]. Universiteit Utrecht; 2012. Available from: http://dspace.library.uu.nl:8080/handle/1874/289411


University of Georgia

23. Castillo, Julio Cesar. Spatio-temporal characterization of the insulin signaling cascade and its role in regulating hemocyte proliferation in Aedes aegypti.

Degree: PhD, Entomology, 2010, University of Georgia

 Hemocytes are central for cell based immunity. In this study, I compared an improved technique (this study) to collect hemocytes from mosquitoes to other welle… (more)

Subjects/Keywords: insulin-like peptides; ILP; hemocytes; MIR; insulin receptor; mosquito; Aedes aegypti; Anopheles gambiae; Drosophila melanogaster; cell proliferation.

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APA (6th Edition):

Castillo, J. C. (2010). Spatio-temporal characterization of the insulin signaling cascade and its role in regulating hemocyte proliferation in Aedes aegypti. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/castillo_julio_c_201012_phd

Chicago Manual of Style (16th Edition):

Castillo, Julio Cesar. “Spatio-temporal characterization of the insulin signaling cascade and its role in regulating hemocyte proliferation in Aedes aegypti.” 2010. Doctoral Dissertation, University of Georgia. Accessed April 19, 2019. http://purl.galileo.usg.edu/uga_etd/castillo_julio_c_201012_phd.

MLA Handbook (7th Edition):

Castillo, Julio Cesar. “Spatio-temporal characterization of the insulin signaling cascade and its role in regulating hemocyte proliferation in Aedes aegypti.” 2010. Web. 19 Apr 2019.

Vancouver:

Castillo JC. Spatio-temporal characterization of the insulin signaling cascade and its role in regulating hemocyte proliferation in Aedes aegypti. [Internet] [Doctoral dissertation]. University of Georgia; 2010. [cited 2019 Apr 19]. Available from: http://purl.galileo.usg.edu/uga_etd/castillo_julio_c_201012_phd.

Council of Science Editors:

Castillo JC. Spatio-temporal characterization of the insulin signaling cascade and its role in regulating hemocyte proliferation in Aedes aegypti. [Doctoral Dissertation]. University of Georgia; 2010. Available from: http://purl.galileo.usg.edu/uga_etd/castillo_julio_c_201012_phd


Univerzitet u Beogradu

24. Robajac, Dragana B., 1985-. N-glikom membranskih proteina i receptora za insulin i faktore rasta slične insulinu, izolovanih iz humane placente u različitim (pato)fiziološkim stanjima.

Degree: Hemijski fakultet, 2016, Univerzitet u Beogradu

Biohemija - Biohemija proteina / Biochemistry - Biochemistry of proteins

Funkcije membranskih proteina su brojne: međućelijska komunikacija, adhezija, signalna transdukcija. Većina membranskih proteina je glikozilovana… (more)

Subjects/Keywords: membrane proteins; N-glycans; N-glycome; insulin receptor; insulin-like growth factor receptors type 1 and 2; gestational changes; aging; placenta

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APA (6th Edition):

Robajac, Dragana B., 1. (2016). N-glikom membranskih proteina i receptora za insulin i faktore rasta slične insulinu, izolovanih iz humane placente u različitim (pato)fiziološkim stanjima. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:12455/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):

Robajac, Dragana B., 1985-. “N-glikom membranskih proteina i receptora za insulin i faktore rasta slične insulinu, izolovanih iz humane placente u različitim (pato)fiziološkim stanjima.” 2016. Thesis, Univerzitet u Beogradu. Accessed April 19, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:12455/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):

Robajac, Dragana B., 1985-. “N-glikom membranskih proteina i receptora za insulin i faktore rasta slične insulinu, izolovanih iz humane placente u različitim (pato)fiziološkim stanjima.” 2016. Web. 19 Apr 2019.

Vancouver:

Robajac, Dragana B. 1. N-glikom membranskih proteina i receptora za insulin i faktore rasta slične insulinu, izolovanih iz humane placente u različitim (pato)fiziološkim stanjima. [Internet] [Thesis]. Univerzitet u Beogradu; 2016. [cited 2019 Apr 19]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:12455/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:

Robajac, Dragana B. 1. N-glikom membranskih proteina i receptora za insulin i faktore rasta slične insulinu, izolovanih iz humane placente u različitim (pato)fiziološkim stanjima. [Thesis]. Univerzitet u Beogradu; 2016. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:12455/bdef:Content/get

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


Ohio University

25. Lesende , Vivian A. RNA Expression of Receptors for Growth Hormone, Insulin-like Growth Factor 1, and Insulin in Mouse Whole Adipose Tissue, Stromal Vascular Fraction, and Adipocytes.

Degree: MS, Biological Sciences (Arts and Sciences), 2015, Ohio University

 Increasing rates of obesity and associated complications worldwide have increased research interest in the complex interplay of hormones, metabolism, and adiposity. There is much evidence… (more)

Subjects/Keywords: Biology; Molecular Biology; adipose tissue; stromal vascular fraction; growth hormone; insulin-like growth factor 1; insulin receptor; mouse models; adipocytes

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APA (6th Edition):

Lesende , V. A. (2015). RNA Expression of Receptors for Growth Hormone, Insulin-like Growth Factor 1, and Insulin in Mouse Whole Adipose Tissue, Stromal Vascular Fraction, and Adipocytes. (Masters Thesis). Ohio University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1440105877

Chicago Manual of Style (16th Edition):

Lesende , Vivian A. “RNA Expression of Receptors for Growth Hormone, Insulin-like Growth Factor 1, and Insulin in Mouse Whole Adipose Tissue, Stromal Vascular Fraction, and Adipocytes.” 2015. Masters Thesis, Ohio University. Accessed April 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1440105877.

MLA Handbook (7th Edition):

Lesende , Vivian A. “RNA Expression of Receptors for Growth Hormone, Insulin-like Growth Factor 1, and Insulin in Mouse Whole Adipose Tissue, Stromal Vascular Fraction, and Adipocytes.” 2015. Web. 19 Apr 2019.

Vancouver:

Lesende VA. RNA Expression of Receptors for Growth Hormone, Insulin-like Growth Factor 1, and Insulin in Mouse Whole Adipose Tissue, Stromal Vascular Fraction, and Adipocytes. [Internet] [Masters thesis]. Ohio University; 2015. [cited 2019 Apr 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1440105877.

Council of Science Editors:

Lesende VA. RNA Expression of Receptors for Growth Hormone, Insulin-like Growth Factor 1, and Insulin in Mouse Whole Adipose Tissue, Stromal Vascular Fraction, and Adipocytes. [Masters Thesis]. Ohio University; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1440105877


Penn State University

26. Reiter, Chad. Constitutive insulin receptor signaling in retina and changes induced by diabetes.

Degree: PhD, Physiology, 2004, Penn State University

 Diabetes is a growing epidemic in Western society which afflicts over 17 million Americans and over 151 million people world wide. People with diabetes are… (more)

Subjects/Keywords: insulin receptor; diabetic retinopathy; retina; insulin; signal transduction

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APA (6th Edition):

Reiter, C. (2004). Constitutive insulin receptor signaling in retina and changes induced by diabetes. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/6379

Chicago Manual of Style (16th Edition):

Reiter, Chad. “Constitutive insulin receptor signaling in retina and changes induced by diabetes.” 2004. Doctoral Dissertation, Penn State University. Accessed April 19, 2019. https://etda.libraries.psu.edu/catalog/6379.

MLA Handbook (7th Edition):

Reiter, Chad. “Constitutive insulin receptor signaling in retina and changes induced by diabetes.” 2004. Web. 19 Apr 2019.

Vancouver:

Reiter C. Constitutive insulin receptor signaling in retina and changes induced by diabetes. [Internet] [Doctoral dissertation]. Penn State University; 2004. [cited 2019 Apr 19]. Available from: https://etda.libraries.psu.edu/catalog/6379.

Council of Science Editors:

Reiter C. Constitutive insulin receptor signaling in retina and changes induced by diabetes. [Doctoral Dissertation]. Penn State University; 2004. Available from: https://etda.libraries.psu.edu/catalog/6379

27. R. Rametta. UN¿AUMENTATA ESPRESSIONE DEL SUBSTRATO DEL RECETTORE DELL¿INSULINA 2 (IRS-2) È ASSOCIATA ALLA STEATOEPATITE E AL DISMETABOLISMO LIPIDICO IN PAZIENTI AFFETTI DA OBESITÀ GRAVE.

Degree: 2013, Università degli Studi di Milano

Design: Studio retrospettivo osservazionale. Soggetti: Abbiamo considerato 71 soggetti obesi (età compresa tra 20 e 68 anni; BMI>40 kg/m2 or BMI>35 kg/m2 in presenza di… (more)

Subjects/Keywords: glucokinase; insulin receptor substrate 2 (IRS2); insulin resistance; lipogenesis; non-alcoholic fatty liver disease (NAFLD); steatosis.; Settore MED/09 - Medicina Interna

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APA (6th Edition):

Rametta, R. (2013). UN¿AUMENTATA ESPRESSIONE DEL SUBSTRATO DEL RECETTORE DELL¿INSULINA 2 (IRS-2) È ASSOCIATA ALLA STEATOEPATITE E AL DISMETABOLISMO LIPIDICO IN PAZIENTI AFFETTI DA OBESITÀ GRAVE. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/219085

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):

Rametta, R.. “UN¿AUMENTATA ESPRESSIONE DEL SUBSTRATO DEL RECETTORE DELL¿INSULINA 2 (IRS-2) È ASSOCIATA ALLA STEATOEPATITE E AL DISMETABOLISMO LIPIDICO IN PAZIENTI AFFETTI DA OBESITÀ GRAVE.” 2013. Thesis, Università degli Studi di Milano. Accessed April 19, 2019. http://hdl.handle.net/2434/219085.

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

MLA Handbook (7th Edition):

Rametta, R.. “UN¿AUMENTATA ESPRESSIONE DEL SUBSTRATO DEL RECETTORE DELL¿INSULINA 2 (IRS-2) È ASSOCIATA ALLA STEATOEPATITE E AL DISMETABOLISMO LIPIDICO IN PAZIENTI AFFETTI DA OBESITÀ GRAVE.” 2013. Web. 19 Apr 2019.

Vancouver:

Rametta R. UN¿AUMENTATA ESPRESSIONE DEL SUBSTRATO DEL RECETTORE DELL¿INSULINA 2 (IRS-2) È ASSOCIATA ALLA STEATOEPATITE E AL DISMETABOLISMO LIPIDICO IN PAZIENTI AFFETTI DA OBESITÀ GRAVE. [Internet] [Thesis]. Università degli Studi di Milano; 2013. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/2434/219085.

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

Council of Science Editors:

Rametta R. UN¿AUMENTATA ESPRESSIONE DEL SUBSTRATO DEL RECETTORE DELL¿INSULINA 2 (IRS-2) È ASSOCIATA ALLA STEATOEPATITE E AL DISMETABOLISMO LIPIDICO IN PAZIENTI AFFETTI DA OBESITÀ GRAVE. [Thesis]. Università degli Studi di Milano; 2013. Available from: http://hdl.handle.net/2434/219085

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


University of British Columbia

28. Lew, Gregory John. Studies on protein phosphorylation in response to insulin in isolated cellular fractions reconstituted with insulin receptors .

Degree: 1988, University of British Columbia

 The mechanism by which insulin and other polypeptide growth factors alter cellular metabolism is not fully understood. In the case of insulin, it is thought… (more)

Subjects/Keywords: Insulin  – Receptors; Protein kinases; Receptor, Insulin; Protein-Tyrosine Kinases

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APA (6th Edition):

Lew, G. J. (1988). Studies on protein phosphorylation in response to insulin in isolated cellular fractions reconstituted with insulin receptors . (Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/27979

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):

Lew, Gregory John. “Studies on protein phosphorylation in response to insulin in isolated cellular fractions reconstituted with insulin receptors .” 1988. Thesis, University of British Columbia. Accessed April 19, 2019. http://hdl.handle.net/2429/27979.

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

MLA Handbook (7th Edition):

Lew, Gregory John. “Studies on protein phosphorylation in response to insulin in isolated cellular fractions reconstituted with insulin receptors .” 1988. Web. 19 Apr 2019.

Vancouver:

Lew GJ. Studies on protein phosphorylation in response to insulin in isolated cellular fractions reconstituted with insulin receptors . [Internet] [Thesis]. University of British Columbia; 1988. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/2429/27979.

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

Council of Science Editors:

Lew GJ. Studies on protein phosphorylation in response to insulin in isolated cellular fractions reconstituted with insulin receptors . [Thesis]. University of British Columbia; 1988. Available from: http://hdl.handle.net/2429/27979

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

29. Sherin, Antony. Muscarinic M1, M3, Nicotinic,GABAA and GABAB Receptor Subtypes Gene Expression in Insulin Induced Hypoglycemic Rat Brain Regions: Functional Regulation through Phospholipase C and CREB Protein.

Degree: Biotechnology, 2010, Cochin University of Science and Technology

In the present study, a detailed investigation on the alterations of muscarinic M1, M3, α7 nicotinic acetylcholine receptor (α7 nAchR), GABA receptors and its subtypes;… (more)

Subjects/Keywords: Muscarinic M1 receptor; Muscarinic M3 receptor; Nicotinic Receptors; GABA Receptors; GABAB Receptors; Insulin; Hypoglycemia; brain; diabetes; Phospholipase C; CREB Protein

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APA (6th Edition):

Sherin, A. (2010). Muscarinic M1, M3, Nicotinic,GABAA and GABAB Receptor Subtypes Gene Expression in Insulin Induced Hypoglycemic Rat Brain Regions: Functional Regulation through Phospholipase C and CREB Protein. (Thesis). Cochin University of Science and Technology. Retrieved from http://dyuthi.cusat.ac.in/purl/2346

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):

Sherin, Antony. “Muscarinic M1, M3, Nicotinic,GABAA and GABAB Receptor Subtypes Gene Expression in Insulin Induced Hypoglycemic Rat Brain Regions: Functional Regulation through Phospholipase C and CREB Protein.” 2010. Thesis, Cochin University of Science and Technology. Accessed April 19, 2019. http://dyuthi.cusat.ac.in/purl/2346.

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

MLA Handbook (7th Edition):

Sherin, Antony. “Muscarinic M1, M3, Nicotinic,GABAA and GABAB Receptor Subtypes Gene Expression in Insulin Induced Hypoglycemic Rat Brain Regions: Functional Regulation through Phospholipase C and CREB Protein.” 2010. Web. 19 Apr 2019.

Vancouver:

Sherin A. Muscarinic M1, M3, Nicotinic,GABAA and GABAB Receptor Subtypes Gene Expression in Insulin Induced Hypoglycemic Rat Brain Regions: Functional Regulation through Phospholipase C and CREB Protein. [Internet] [Thesis]. Cochin University of Science and Technology; 2010. [cited 2019 Apr 19]. Available from: http://dyuthi.cusat.ac.in/purl/2346.

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

Council of Science Editors:

Sherin A. Muscarinic M1, M3, Nicotinic,GABAA and GABAB Receptor Subtypes Gene Expression in Insulin Induced Hypoglycemic Rat Brain Regions: Functional Regulation through Phospholipase C and CREB Protein. [Thesis]. Cochin University of Science and Technology; 2010. Available from: http://dyuthi.cusat.ac.in/purl/2346

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

30. Filippi, Renée Zon. Estudo da expressão das proteínas TFE3 e receptor de insulina nos hepatoblastomas a partir dos achados de expressão gênica.

Degree: PhD, Patologia, 2011, University of São Paulo

O hepatoblastoma é uma neoplasia embrionária hepática que ocorre na faixa pediátrica, rara, sendo bastante heterogênea devido aos seus diferentes componentes epiteliais e mesenquimais. Pouco… (more)

Subjects/Keywords: cDNA microarray; cDNA microarray; Expressão gênica; Gene expression profile; Hepatoblastoma; Hepatoblastoma; Immunohistochemistry; Imuno-histoquímica; Insulin receptor; Receptor de insulina; TFE3; TFE3

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

APA (6th Edition):

Filippi, R. Z. (2011). Estudo da expressão das proteínas TFE3 e receptor de insulina nos hepatoblastomas a partir dos achados de expressão gênica. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5144/tde-26012012-100515/ ;

Chicago Manual of Style (16th Edition):

Filippi, Renée Zon. “Estudo da expressão das proteínas TFE3 e receptor de insulina nos hepatoblastomas a partir dos achados de expressão gênica.” 2011. Doctoral Dissertation, University of São Paulo. Accessed April 19, 2019. http://www.teses.usp.br/teses/disponiveis/5/5144/tde-26012012-100515/ ;.

MLA Handbook (7th Edition):

Filippi, Renée Zon. “Estudo da expressão das proteínas TFE3 e receptor de insulina nos hepatoblastomas a partir dos achados de expressão gênica.” 2011. Web. 19 Apr 2019.

Vancouver:

Filippi RZ. Estudo da expressão das proteínas TFE3 e receptor de insulina nos hepatoblastomas a partir dos achados de expressão gênica. [Internet] [Doctoral dissertation]. University of São Paulo; 2011. [cited 2019 Apr 19]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5144/tde-26012012-100515/ ;.

Council of Science Editors:

Filippi RZ. Estudo da expressão das proteínas TFE3 e receptor de insulina nos hepatoblastomas a partir dos achados de expressão gênica. [Doctoral Dissertation]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/5/5144/tde-26012012-100515/ ;

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