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You searched for subject:( 1 25D3 MARRS receptor). Showing records 1 – 30 of 32125 total matches.

[1] [2] [3] [4] [5] … [1071]

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Utah State University

1. Tunsophon, Sakara. Role of Protein Kinase C Isotypes in 1,25-Dihydroxyvitamin D3 Mediated Signal Transduction Through the 1,25D3 Membrane Associated, Rapid Response Steroid Binding Receptors in Chick Intestinal Cells.

Degree: PhD, Nutrition, Dietetics, and Food Sciences, 2010, Utah State University

 It is now accepted that 1,25(OH)2D3 mediates its rapid actions on the control of phosphate and calcium homeostasis through its membrane receptor termed the 1,25D3-MARRS(more)

Subjects/Keywords: 1; 25 dihydroxyvitamin D3; 1; 25D3-MARRS receptor; PKC isotypes; Dietetics and Clinical Nutrition; Medicine and Health Sciences; Molecular Biology

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APA (6th Edition):

Tunsophon, S. (2010). Role of Protein Kinase C Isotypes in 1,25-Dihydroxyvitamin D3 Mediated Signal Transduction Through the 1,25D3 Membrane Associated, Rapid Response Steroid Binding Receptors in Chick Intestinal Cells. (Doctoral Dissertation). Utah State University. Retrieved from https://digitalcommons.usu.edu/etd/705

Chicago Manual of Style (16th Edition):

Tunsophon, Sakara. “Role of Protein Kinase C Isotypes in 1,25-Dihydroxyvitamin D3 Mediated Signal Transduction Through the 1,25D3 Membrane Associated, Rapid Response Steroid Binding Receptors in Chick Intestinal Cells.” 2010. Doctoral Dissertation, Utah State University. Accessed August 24, 2019. https://digitalcommons.usu.edu/etd/705.

MLA Handbook (7th Edition):

Tunsophon, Sakara. “Role of Protein Kinase C Isotypes in 1,25-Dihydroxyvitamin D3 Mediated Signal Transduction Through the 1,25D3 Membrane Associated, Rapid Response Steroid Binding Receptors in Chick Intestinal Cells.” 2010. Web. 24 Aug 2019.

Vancouver:

Tunsophon S. Role of Protein Kinase C Isotypes in 1,25-Dihydroxyvitamin D3 Mediated Signal Transduction Through the 1,25D3 Membrane Associated, Rapid Response Steroid Binding Receptors in Chick Intestinal Cells. [Internet] [Doctoral dissertation]. Utah State University; 2010. [cited 2019 Aug 24]. Available from: https://digitalcommons.usu.edu/etd/705.

Council of Science Editors:

Tunsophon S. Role of Protein Kinase C Isotypes in 1,25-Dihydroxyvitamin D3 Mediated Signal Transduction Through the 1,25D3 Membrane Associated, Rapid Response Steroid Binding Receptors in Chick Intestinal Cells. [Doctoral Dissertation]. Utah State University; 2010. Available from: https://digitalcommons.usu.edu/etd/705


University of Guelph

2. Wilkin, Allison. An Investigation into the Role of the MARRS Receptor in Murine Mammary Gland Growth and Development .

Degree: 2019, University of Guelph

 Vitamin D has been implicated in mammary gland development, however nothing is known about the role of the second 1,25-dihydroxyvitamin D3 (1,25D3) receptor MARRS and… (more)

Subjects/Keywords: vitamin D; mammary gland; 1,25D3-MARRS receptor; Vitamin D Receptor; ERp57

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APA (6th Edition):

Wilkin, A. (2019). An Investigation into the Role of the MARRS Receptor in Murine Mammary Gland Growth and Development . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/16850

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):

Wilkin, Allison. “An Investigation into the Role of the MARRS Receptor in Murine Mammary Gland Growth and Development .” 2019. Thesis, University of Guelph. Accessed August 24, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/16850.

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

MLA Handbook (7th Edition):

Wilkin, Allison. “An Investigation into the Role of the MARRS Receptor in Murine Mammary Gland Growth and Development .” 2019. Web. 24 Aug 2019.

Vancouver:

Wilkin A. An Investigation into the Role of the MARRS Receptor in Murine Mammary Gland Growth and Development . [Internet] [Thesis]. University of Guelph; 2019. [cited 2019 Aug 24]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/16850.

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

Council of Science Editors:

Wilkin A. An Investigation into the Role of the MARRS Receptor in Murine Mammary Gland Growth and Development . [Thesis]. University of Guelph; 2019. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/16850

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

3. Gu, Hongbo. Mass Spectrometry Analysis of Potential Biomarker Proteins.

Degree: PhD, Chemistry, 2012, Brown University

 Towards the full understanding the physiology of human Sigma-1 receptor (Sig-1R), we developed a novel ligand-based enrichment strategy and mass spectrometry analysis of the receptor.… (more)

Subjects/Keywords: Sigma-1 receptor

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APA (6th Edition):

Gu, H. (2012). Mass Spectrometry Analysis of Potential Biomarker Proteins. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:297583/

Chicago Manual of Style (16th Edition):

Gu, Hongbo. “Mass Spectrometry Analysis of Potential Biomarker Proteins.” 2012. Doctoral Dissertation, Brown University. Accessed August 24, 2019. https://repository.library.brown.edu/studio/item/bdr:297583/.

MLA Handbook (7th Edition):

Gu, Hongbo. “Mass Spectrometry Analysis of Potential Biomarker Proteins.” 2012. Web. 24 Aug 2019.

Vancouver:

Gu H. Mass Spectrometry Analysis of Potential Biomarker Proteins. [Internet] [Doctoral dissertation]. Brown University; 2012. [cited 2019 Aug 24]. Available from: https://repository.library.brown.edu/studio/item/bdr:297583/.

Council of Science Editors:

Gu H. Mass Spectrometry Analysis of Potential Biomarker Proteins. [Doctoral Dissertation]. Brown University; 2012. Available from: https://repository.library.brown.edu/studio/item/bdr:297583/


Wake Forest University

4. Alzayadneh, Ebaa M. A ROLE FOR ANGIOTENSIN-(1-7) TO ATTENUATE ADVANCED GLYCATION END PRODUCT -INDUCED MYOFIBROBLAST TRANSITION IN THE NRK-52E RENAL PROXIMAL TUBULE CELL LINE.

Degree: 2014, Wake Forest University

 There is compelling evidence for a role of intracellular renin-angiotensin system (RAS) in cell signaling, function and cardiovascular pathologies. Diabetic nephropathy is a very common… (more)

Subjects/Keywords: Ang-(1-7)-Mas receptor

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APA (6th Edition):

Alzayadneh, E. M. (2014). A ROLE FOR ANGIOTENSIN-(1-7) TO ATTENUATE ADVANCED GLYCATION END PRODUCT -INDUCED MYOFIBROBLAST TRANSITION IN THE NRK-52E RENAL PROXIMAL TUBULE CELL LINE. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/39401

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):

Alzayadneh, Ebaa M. “A ROLE FOR ANGIOTENSIN-(1-7) TO ATTENUATE ADVANCED GLYCATION END PRODUCT -INDUCED MYOFIBROBLAST TRANSITION IN THE NRK-52E RENAL PROXIMAL TUBULE CELL LINE.” 2014. Thesis, Wake Forest University. Accessed August 24, 2019. http://hdl.handle.net/10339/39401.

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

MLA Handbook (7th Edition):

Alzayadneh, Ebaa M. “A ROLE FOR ANGIOTENSIN-(1-7) TO ATTENUATE ADVANCED GLYCATION END PRODUCT -INDUCED MYOFIBROBLAST TRANSITION IN THE NRK-52E RENAL PROXIMAL TUBULE CELL LINE.” 2014. Web. 24 Aug 2019.

Vancouver:

Alzayadneh EM. A ROLE FOR ANGIOTENSIN-(1-7) TO ATTENUATE ADVANCED GLYCATION END PRODUCT -INDUCED MYOFIBROBLAST TRANSITION IN THE NRK-52E RENAL PROXIMAL TUBULE CELL LINE. [Internet] [Thesis]. Wake Forest University; 2014. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/10339/39401.

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

Council of Science Editors:

Alzayadneh EM. A ROLE FOR ANGIOTENSIN-(1-7) TO ATTENUATE ADVANCED GLYCATION END PRODUCT -INDUCED MYOFIBROBLAST TRANSITION IN THE NRK-52E RENAL PROXIMAL TUBULE CELL LINE. [Thesis]. Wake Forest University; 2014. Available from: http://hdl.handle.net/10339/39401

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

5. Ellens, Elizabeth Rose. Evolution of the Growth Hormone Receptor: Insights Into the Molecular Basis of the Physiologically Pleiotropic Nature of the Growth Hormone Receptor.

Degree: MS, Biological Sciences, 2014, North Dakota State University

 One of the oldest, extant, lineages of vertebrates, the sea lamprey, was used to clarify the evolutionary origin and divergence of the growth hormone receptor(more)

Subjects/Keywords: Evolution; Growth hormone receptor; Lamprey; Prolactin receptor; Somatolactin receptor; Type-1 cytokine receptor

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APA (6th Edition):

Ellens, E. R. (2014). Evolution of the Growth Hormone Receptor: Insights Into the Molecular Basis of the Physiologically Pleiotropic Nature of the Growth Hormone Receptor. (Masters Thesis). North Dakota State University. Retrieved from http://hdl.handle.net/10365/26654

Chicago Manual of Style (16th Edition):

Ellens, Elizabeth Rose. “Evolution of the Growth Hormone Receptor: Insights Into the Molecular Basis of the Physiologically Pleiotropic Nature of the Growth Hormone Receptor.” 2014. Masters Thesis, North Dakota State University. Accessed August 24, 2019. http://hdl.handle.net/10365/26654.

MLA Handbook (7th Edition):

Ellens, Elizabeth Rose. “Evolution of the Growth Hormone Receptor: Insights Into the Molecular Basis of the Physiologically Pleiotropic Nature of the Growth Hormone Receptor.” 2014. Web. 24 Aug 2019.

Vancouver:

Ellens ER. Evolution of the Growth Hormone Receptor: Insights Into the Molecular Basis of the Physiologically Pleiotropic Nature of the Growth Hormone Receptor. [Internet] [Masters thesis]. North Dakota State University; 2014. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/10365/26654.

Council of Science Editors:

Ellens ER. Evolution of the Growth Hormone Receptor: Insights Into the Molecular Basis of the Physiologically Pleiotropic Nature of the Growth Hormone Receptor. [Masters Thesis]. North Dakota State University; 2014. Available from: http://hdl.handle.net/10365/26654


Universitat Rovira i Virgili

6. Saavedra García, Paula. FABP4: interactions with endothelial cell plasma membrane and effects on vascular smooth muscle cells.

Degree: Departament de Medicina i Cirurgia, 2016, Universitat Rovira i Virgili

 Fatty acid-binding protein 4 (FABP4) is an adipose tissue-secreted adipokine that is involved in the regulation of energetic metabolism and inflammation. Increased levels of circulating… (more)

Subjects/Keywords: FABP4; Receptor de membrana; Citoqueratina 1; FABP4; Receptor de membrana; Citoqueratina 1; FABP4; Cell surface receptor; Cytokeratin 1; 577

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APA (6th Edition):

Saavedra García, P. (2016). FABP4: interactions with endothelial cell plasma membrane and effects on vascular smooth muscle cells. (Thesis). Universitat Rovira i Virgili. Retrieved from http://hdl.handle.net/10803/348560

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):

Saavedra García, Paula. “FABP4: interactions with endothelial cell plasma membrane and effects on vascular smooth muscle cells.” 2016. Thesis, Universitat Rovira i Virgili. Accessed August 24, 2019. http://hdl.handle.net/10803/348560.

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

MLA Handbook (7th Edition):

Saavedra García, Paula. “FABP4: interactions with endothelial cell plasma membrane and effects on vascular smooth muscle cells.” 2016. Web. 24 Aug 2019.

Vancouver:

Saavedra García P. FABP4: interactions with endothelial cell plasma membrane and effects on vascular smooth muscle cells. [Internet] [Thesis]. Universitat Rovira i Virgili; 2016. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/10803/348560.

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

Council of Science Editors:

Saavedra García P. FABP4: interactions with endothelial cell plasma membrane and effects on vascular smooth muscle cells. [Thesis]. Universitat Rovira i Virgili; 2016. Available from: http://hdl.handle.net/10803/348560

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


University of Alberta

7. Li, Nicholas L. Regulation of the inhibitory receptor LIR-1 in human natural killer cells.

Degree: PhD, Department of Medical Microbiology and Immunology, 2013, University of Alberta

 Natural killer (NK) cells are innate immune lymphocytes that provide protection against virus infection and transformation. The cytolytic activity of NK cells is controlled by… (more)

Subjects/Keywords: Natural Killer Cells; LIR-1; Inhibitory Receptor

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APA (6th Edition):

Li, N. L. (2013). Regulation of the inhibitory receptor LIR-1 in human natural killer cells. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/gt54kn99q

Chicago Manual of Style (16th Edition):

Li, Nicholas L. “Regulation of the inhibitory receptor LIR-1 in human natural killer cells.” 2013. Doctoral Dissertation, University of Alberta. Accessed August 24, 2019. https://era.library.ualberta.ca/files/gt54kn99q.

MLA Handbook (7th Edition):

Li, Nicholas L. “Regulation of the inhibitory receptor LIR-1 in human natural killer cells.” 2013. Web. 24 Aug 2019.

Vancouver:

Li NL. Regulation of the inhibitory receptor LIR-1 in human natural killer cells. [Internet] [Doctoral dissertation]. University of Alberta; 2013. [cited 2019 Aug 24]. Available from: https://era.library.ualberta.ca/files/gt54kn99q.

Council of Science Editors:

Li NL. Regulation of the inhibitory receptor LIR-1 in human natural killer cells. [Doctoral Dissertation]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/gt54kn99q


Penn State University

8. Woll, Matthew Patrick. CHARACTERIZATION OF THE D2 DOPAMINE RECEPTOR/NEURONAL CALCIUM SENSOR-1 INTERACTION.

Degree: PhD, Pharmacology, 2009, Penn State University

 Abnormalities in D2 dopamine receptor (D2R) neurotransmission are implicated in a number of neurological and psychiatric conditions including bipolar disorder, depression, and schizophrenia. Studies suggest… (more)

Subjects/Keywords: Fluorescence Polarization; D2 Dopamine Receptor; NCS-1

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APA (6th Edition):

Woll, M. P. (2009). CHARACTERIZATION OF THE D2 DOPAMINE RECEPTOR/NEURONAL CALCIUM SENSOR-1 INTERACTION. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/10232

Chicago Manual of Style (16th Edition):

Woll, Matthew Patrick. “CHARACTERIZATION OF THE D2 DOPAMINE RECEPTOR/NEURONAL CALCIUM SENSOR-1 INTERACTION.” 2009. Doctoral Dissertation, Penn State University. Accessed August 24, 2019. https://etda.libraries.psu.edu/catalog/10232.

MLA Handbook (7th Edition):

Woll, Matthew Patrick. “CHARACTERIZATION OF THE D2 DOPAMINE RECEPTOR/NEURONAL CALCIUM SENSOR-1 INTERACTION.” 2009. Web. 24 Aug 2019.

Vancouver:

Woll MP. CHARACTERIZATION OF THE D2 DOPAMINE RECEPTOR/NEURONAL CALCIUM SENSOR-1 INTERACTION. [Internet] [Doctoral dissertation]. Penn State University; 2009. [cited 2019 Aug 24]. Available from: https://etda.libraries.psu.edu/catalog/10232.

Council of Science Editors:

Woll MP. CHARACTERIZATION OF THE D2 DOPAMINE RECEPTOR/NEURONAL CALCIUM SENSOR-1 INTERACTION. [Doctoral Dissertation]. Penn State University; 2009. Available from: https://etda.libraries.psu.edu/catalog/10232

9. Glasper, James Edward. Exploration of the molecular mechanisms of cognitive dysfunction in schizophrenia using the sub-chronic PCP rodent model.

Degree: 2015, University of Manchester

 Cognitive dysfunction is a core symptom of schizophrenia, which is poorly treated by current antipsychotic medication. Deficits in the GABAergic system, as demonstrated by convergent… (more)

Subjects/Keywords: Rodent; Phencyclidine; Cognition; GABA; Sigma-1 receptor

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APA (6th Edition):

Glasper, J. E. (2015). Exploration of the molecular mechanisms of cognitive dysfunction in schizophrenia using the sub-chronic PCP rodent model. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:260357

Chicago Manual of Style (16th Edition):

Glasper, James Edward. “Exploration of the molecular mechanisms of cognitive dysfunction in schizophrenia using the sub-chronic PCP rodent model.” 2015. Doctoral Dissertation, University of Manchester. Accessed August 24, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:260357.

MLA Handbook (7th Edition):

Glasper, James Edward. “Exploration of the molecular mechanisms of cognitive dysfunction in schizophrenia using the sub-chronic PCP rodent model.” 2015. Web. 24 Aug 2019.

Vancouver:

Glasper JE. Exploration of the molecular mechanisms of cognitive dysfunction in schizophrenia using the sub-chronic PCP rodent model. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2019 Aug 24]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:260357.

Council of Science Editors:

Glasper JE. Exploration of the molecular mechanisms of cognitive dysfunction in schizophrenia using the sub-chronic PCP rodent model. [Doctoral Dissertation]. University of Manchester; 2015. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:260357


University of Ottawa

10. Cherid, Hafsa. Regions of the CD127 Cytoplasmic Tail Necessary for HIV-1 Tat Binding .

Degree: 2014, University of Ottawa

 Impaired cell mediated immunity is the clinical hallmark of HIV infection yet the manner in which CD8 T-cells are disabled is not yet fully understood.… (more)

Subjects/Keywords: HIV-1 Tat; IL-7 receptor; CD127

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APA (6th Edition):

Cherid, H. (2014). Regions of the CD127 Cytoplasmic Tail Necessary for HIV-1 Tat Binding . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/31556

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):

Cherid, Hafsa. “Regions of the CD127 Cytoplasmic Tail Necessary for HIV-1 Tat Binding .” 2014. Thesis, University of Ottawa. Accessed August 24, 2019. http://hdl.handle.net/10393/31556.

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

MLA Handbook (7th Edition):

Cherid, Hafsa. “Regions of the CD127 Cytoplasmic Tail Necessary for HIV-1 Tat Binding .” 2014. Web. 24 Aug 2019.

Vancouver:

Cherid H. Regions of the CD127 Cytoplasmic Tail Necessary for HIV-1 Tat Binding . [Internet] [Thesis]. University of Ottawa; 2014. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/10393/31556.

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

Council of Science Editors:

Cherid H. Regions of the CD127 Cytoplasmic Tail Necessary for HIV-1 Tat Binding . [Thesis]. University of Ottawa; 2014. Available from: http://hdl.handle.net/10393/31556

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


University of Miami

11. Qiu, Feng. Regulation of Pannexin 1 Channels by ATP.

Degree: PhD, Physiology and Biophysics (Medicine), 2010, University of Miami

  Pannexins represent a recently discovered second family of gap junction proteins in vertebrates. However, instead of forming intercellular gap junction channels like connexins, pannexins… (more)

Subjects/Keywords: Pannexin 1; ATP; Negative Feedback; P2X7 Receptor

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APA (6th Edition):

Qiu, F. (2010). Regulation of Pannexin 1 Channels by ATP. (Doctoral Dissertation). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_dissertations/394

Chicago Manual of Style (16th Edition):

Qiu, Feng. “Regulation of Pannexin 1 Channels by ATP.” 2010. Doctoral Dissertation, University of Miami. Accessed August 24, 2019. https://scholarlyrepository.miami.edu/oa_dissertations/394.

MLA Handbook (7th Edition):

Qiu, Feng. “Regulation of Pannexin 1 Channels by ATP.” 2010. Web. 24 Aug 2019.

Vancouver:

Qiu F. Regulation of Pannexin 1 Channels by ATP. [Internet] [Doctoral dissertation]. University of Miami; 2010. [cited 2019 Aug 24]. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/394.

Council of Science Editors:

Qiu F. Regulation of Pannexin 1 Channels by ATP. [Doctoral Dissertation]. University of Miami; 2010. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/394


University of Toronto

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

Degree: 2013, University of Toronto

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Huang, Xinyi. “The Identification of Novel Proteins that Interact with the GLP-1 Receptor and Restrain its Activity.” 2013. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/42870.

MLA Handbook (7th Edition):

Huang, Xinyi. “The Identification of Novel Proteins that Interact with the GLP-1 Receptor and Restrain its Activity.” 2013. Web. 24 Aug 2019.

Vancouver:

Huang X. The Identification of Novel Proteins that Interact with the GLP-1 Receptor and Restrain its Activity. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/42870.

Council of Science Editors:

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


University of Ottawa

13. McCann, Kieran. An Investigation of Sigma-1 Receptor Involvement in Glutamatergic Synaptic Physiology, Implications for Alzheimer’s Disease .

Degree: 2015, University of Ottawa

 The sigma-1 receptor (sig-1R) is a unique endoplasmic reticulum (ER) chaperone protein that interacts with a variety of voltage- and ligand-gated ion channels, which are… (more)

Subjects/Keywords: Sigma-1 receptor; NMDA Receptor; Alzheimer's Disease; Hippocampus; Electrophysiology; Pyramidal neuron

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APA (6th Edition):

McCann, K. (2015). An Investigation of Sigma-1 Receptor Involvement in Glutamatergic Synaptic Physiology, Implications for Alzheimer’s Disease . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/32344

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):

McCann, Kieran. “An Investigation of Sigma-1 Receptor Involvement in Glutamatergic Synaptic Physiology, Implications for Alzheimer’s Disease .” 2015. Thesis, University of Ottawa. Accessed August 24, 2019. http://hdl.handle.net/10393/32344.

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

MLA Handbook (7th Edition):

McCann, Kieran. “An Investigation of Sigma-1 Receptor Involvement in Glutamatergic Synaptic Physiology, Implications for Alzheimer’s Disease .” 2015. Web. 24 Aug 2019.

Vancouver:

McCann K. An Investigation of Sigma-1 Receptor Involvement in Glutamatergic Synaptic Physiology, Implications for Alzheimer’s Disease . [Internet] [Thesis]. University of Ottawa; 2015. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/10393/32344.

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

Council of Science Editors:

McCann K. An Investigation of Sigma-1 Receptor Involvement in Glutamatergic Synaptic Physiology, Implications for Alzheimer’s Disease . [Thesis]. University of Ottawa; 2015. Available from: http://hdl.handle.net/10393/32344

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

14. Figueiredo, Ana Sofia Soares. Insulinas e carcinogénese: questões levantadas pelas insulinas humanas recombinantes em utilização terapêutica.

Degree: 2010, RCAAP

Dissertação de mest., Ciências Farmacêuticas, Faculdade de Ciências e Tecnologia, Univ. do Algarve, 2010

Mundialmente, a Diabetes afecta mais de 200 milhões de pessoas. Cerca… (more)

Subjects/Keywords: Análogos de insulina; Cancro; Diabetes; Receptor da insulina; Receptor do IGF-1; Insulina; IGF-1

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APA (6th Edition):

Figueiredo, A. S. S. (2010). Insulinas e carcinogénese: questões levantadas pelas insulinas humanas recombinantes em utilização terapêutica. (Thesis). RCAAP. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:sapientia.ualg.pt:10400.1/1659

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):

Figueiredo, Ana Sofia Soares. “Insulinas e carcinogénese: questões levantadas pelas insulinas humanas recombinantes em utilização terapêutica.” 2010. Thesis, RCAAP. Accessed August 24, 2019. http://www.rcaap.pt/detail.jsp?id=oai:sapientia.ualg.pt:10400.1/1659.

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

MLA Handbook (7th Edition):

Figueiredo, Ana Sofia Soares. “Insulinas e carcinogénese: questões levantadas pelas insulinas humanas recombinantes em utilização terapêutica.” 2010. Web. 24 Aug 2019.

Vancouver:

Figueiredo ASS. Insulinas e carcinogénese: questões levantadas pelas insulinas humanas recombinantes em utilização terapêutica. [Internet] [Thesis]. RCAAP; 2010. [cited 2019 Aug 24]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:sapientia.ualg.pt:10400.1/1659.

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

Council of Science Editors:

Figueiredo ASS. Insulinas e carcinogénese: questões levantadas pelas insulinas humanas recombinantes em utilização terapêutica. [Thesis]. RCAAP; 2010. Available from: http://www.rcaap.pt/detail.jsp?id=oai:sapientia.ualg.pt:10400.1/1659

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


NSYSU

15. Wang, Shang-ying. Type-1 Interleukin-1 Receptor is Essential for Host Defense Against Pseudomonas aeruginosa-induced Pneumonia.

Degree: Master, Biological Sciences, 2009, NSYSU

 IL-1 is an essential pro-inflammatory factor in inflammation response. The effect of IL-1 is through binding to the IL-1 receptor that triggers the following signal… (more)

Subjects/Keywords: pseudomonas aeruginosa; pneumonia; Type-1 Interleukin-1 receptor

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

APA (6th Edition):

Wang, S. (2009). Type-1 Interleukin-1 Receptor is Essential for Host Defense Against Pseudomonas aeruginosa-induced Pneumonia. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0826109-152046

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

Chicago Manual of Style (16th Edition):

Wang, Shang-ying. “Type-1 Interleukin-1 Receptor is Essential for Host Defense Against Pseudomonas aeruginosa-induced Pneumonia.” 2009. Thesis, NSYSU. Accessed August 24, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0826109-152046.

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

MLA Handbook (7th Edition):

Wang, Shang-ying. “Type-1 Interleukin-1 Receptor is Essential for Host Defense Against Pseudomonas aeruginosa-induced Pneumonia.” 2009. Web. 24 Aug 2019.

Vancouver:

Wang S. Type-1 Interleukin-1 Receptor is Essential for Host Defense Against Pseudomonas aeruginosa-induced Pneumonia. [Internet] [Thesis]. NSYSU; 2009. [cited 2019 Aug 24]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0826109-152046.

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

Council of Science Editors:

Wang S. Type-1 Interleukin-1 Receptor is Essential for Host Defense Against Pseudomonas aeruginosa-induced Pneumonia. [Thesis]. NSYSU; 2009. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0826109-152046

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


Université de Montréal

16. Quiniou, Christiane. Développement de modulateurs allostériques peptidiques inhibiteurs de l’activité des récepteurs de l’interleukine 1 et de la vasopressine .

Degree: 2011, Université de Montréal

 L’approche Module X a été créée dans le but de concevoir de petits peptides modulateurs ayant des propriétés allostériques. Module X reproduit de petites parties… (more)

Subjects/Keywords: Allostérisme; Peptides; Allosteric; Inflammation; Interleukin-1; Récepteur; Allosterism; Receptor; Interleukine-1

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

APA (6th Edition):

Quiniou, C. (2011). Développement de modulateurs allostériques peptidiques inhibiteurs de l’activité des récepteurs de l’interleukine 1 et de la vasopressine . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/6097

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):

Quiniou, Christiane. “Développement de modulateurs allostériques peptidiques inhibiteurs de l’activité des récepteurs de l’interleukine 1 et de la vasopressine .” 2011. Thesis, Université de Montréal. Accessed August 24, 2019. http://hdl.handle.net/1866/6097.

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

MLA Handbook (7th Edition):

Quiniou, Christiane. “Développement de modulateurs allostériques peptidiques inhibiteurs de l’activité des récepteurs de l’interleukine 1 et de la vasopressine .” 2011. Web. 24 Aug 2019.

Vancouver:

Quiniou C. Développement de modulateurs allostériques peptidiques inhibiteurs de l’activité des récepteurs de l’interleukine 1 et de la vasopressine . [Internet] [Thesis]. Université de Montréal; 2011. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1866/6097.

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

Council of Science Editors:

Quiniou C. Développement de modulateurs allostériques peptidiques inhibiteurs de l’activité des récepteurs de l’interleukine 1 et de la vasopressine . [Thesis]. Université de Montréal; 2011. Available from: http://hdl.handle.net/1866/6097

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


University of Saskatchewan

17. Xiao, Shujun (Jennifer) 1991-. Antitumor effect of the combination of exogenous sphingosine-1-phosphate(S1P), S1P receptor 1(S1PR1) antibody and carboplatin against human breast cancer cells.

Degree: 2018, University of Saskatchewan

 Breast cancer is the third most common cancer in Canada. Even though the morbidity and mortality rates have reduced in recent years because of early… (more)

Subjects/Keywords: Breast cancer; sphingosine-1-phosphate; S1P receptor 1; carboplatin

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APA (6th Edition):

Xiao, S. (. 1. (2018). Antitumor effect of the combination of exogenous sphingosine-1-phosphate(S1P), S1P receptor 1(S1PR1) antibody and carboplatin against human breast cancer cells. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/11253

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):

Xiao, Shujun (Jennifer) 1991-. “Antitumor effect of the combination of exogenous sphingosine-1-phosphate(S1P), S1P receptor 1(S1PR1) antibody and carboplatin against human breast cancer cells.” 2018. Thesis, University of Saskatchewan. Accessed August 24, 2019. http://hdl.handle.net/10388/11253.

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

MLA Handbook (7th Edition):

Xiao, Shujun (Jennifer) 1991-. “Antitumor effect of the combination of exogenous sphingosine-1-phosphate(S1P), S1P receptor 1(S1PR1) antibody and carboplatin against human breast cancer cells.” 2018. Web. 24 Aug 2019.

Vancouver:

Xiao S(1. Antitumor effect of the combination of exogenous sphingosine-1-phosphate(S1P), S1P receptor 1(S1PR1) antibody and carboplatin against human breast cancer cells. [Internet] [Thesis]. University of Saskatchewan; 2018. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/10388/11253.

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

Council of Science Editors:

Xiao S(1. Antitumor effect of the combination of exogenous sphingosine-1-phosphate(S1P), S1P receptor 1(S1PR1) antibody and carboplatin against human breast cancer cells. [Thesis]. University of Saskatchewan; 2018. Available from: http://hdl.handle.net/10388/11253

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


University of Adelaide

18. Pham, Duyen H. Gene regulation by Sphingosine kinase.

Degree: 2012, University of Adelaide

 Sphingosine kinases (SKs) are lipid kinases that catalyse the phosphorylation of sphingosine to form sphingosine-1-phosphate (S1P), a bioactive phospholipid that plays important roles in a… (more)

Subjects/Keywords: gene; sphingosine kinase; sphingosine 1-phosphate; transferrin receptor 1

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APA (6th Edition):

Pham, D. H. (2012). Gene regulation by Sphingosine kinase. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/86477

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):

Pham, Duyen H. “Gene regulation by Sphingosine kinase.” 2012. Thesis, University of Adelaide. Accessed August 24, 2019. http://hdl.handle.net/2440/86477.

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

MLA Handbook (7th Edition):

Pham, Duyen H. “Gene regulation by Sphingosine kinase.” 2012. Web. 24 Aug 2019.

Vancouver:

Pham DH. Gene regulation by Sphingosine kinase. [Internet] [Thesis]. University of Adelaide; 2012. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/2440/86477.

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

Council of Science Editors:

Pham DH. Gene regulation by Sphingosine kinase. [Thesis]. University of Adelaide; 2012. Available from: http://hdl.handle.net/2440/86477

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

19. Paoletti, Audrey. Étude des étapes précoces de l’infection par le VIH-1 : identification d’un nouveau point de contrôle immunitaire immunitaire impliquant le récepteur P2Y2 et la protéine NLRP3 : Study Of The Early Steps Of HIV-1 Infection : Identification Of A New Immune Checkpoint Involving P2Y2 And NLRP3.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2015, Paris Saclay

Plus de 34 millions de personnes dans le monde vivent avec le virus de l’immunodéficience humaine de type 1 (VIH-1). Cette pandémie est partiellement contrôlée… (more)

Subjects/Keywords: Vih-1; Récepteur purinergique; Inflammasome; Hiv-1; Purinergic receptor; Inflammasome

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APA (6th Edition):

Paoletti, A. (2015). Étude des étapes précoces de l’infection par le VIH-1 : identification d’un nouveau point de contrôle immunitaire immunitaire impliquant le récepteur P2Y2 et la protéine NLRP3 : Study Of The Early Steps Of HIV-1 Infection : Identification Of A New Immune Checkpoint Involving P2Y2 And NLRP3. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2015SACLS240

Chicago Manual of Style (16th Edition):

Paoletti, Audrey. “Étude des étapes précoces de l’infection par le VIH-1 : identification d’un nouveau point de contrôle immunitaire immunitaire impliquant le récepteur P2Y2 et la protéine NLRP3 : Study Of The Early Steps Of HIV-1 Infection : Identification Of A New Immune Checkpoint Involving P2Y2 And NLRP3.” 2015. Doctoral Dissertation, Paris Saclay. Accessed August 24, 2019. http://www.theses.fr/2015SACLS240.

MLA Handbook (7th Edition):

Paoletti, Audrey. “Étude des étapes précoces de l’infection par le VIH-1 : identification d’un nouveau point de contrôle immunitaire immunitaire impliquant le récepteur P2Y2 et la protéine NLRP3 : Study Of The Early Steps Of HIV-1 Infection : Identification Of A New Immune Checkpoint Involving P2Y2 And NLRP3.” 2015. Web. 24 Aug 2019.

Vancouver:

Paoletti A. Étude des étapes précoces de l’infection par le VIH-1 : identification d’un nouveau point de contrôle immunitaire immunitaire impliquant le récepteur P2Y2 et la protéine NLRP3 : Study Of The Early Steps Of HIV-1 Infection : Identification Of A New Immune Checkpoint Involving P2Y2 And NLRP3. [Internet] [Doctoral dissertation]. Paris Saclay; 2015. [cited 2019 Aug 24]. Available from: http://www.theses.fr/2015SACLS240.

Council of Science Editors:

Paoletti A. Étude des étapes précoces de l’infection par le VIH-1 : identification d’un nouveau point de contrôle immunitaire immunitaire impliquant le récepteur P2Y2 et la protéine NLRP3 : Study Of The Early Steps Of HIV-1 Infection : Identification Of A New Immune Checkpoint Involving P2Y2 And NLRP3. [Doctoral Dissertation]. Paris Saclay; 2015. Available from: http://www.theses.fr/2015SACLS240


University of California – San Francisco

20. Gertz, Karmela Ramos. Chemical and Genetic Regulation of Nuclear Receptor 5A (NR5A) Sumoylation.

Degree: Biochemistry and Molecular Biology, 2014, University of California – San Francisco

 ABSTRACTSUMO-modification of nuclear proteins has profound effects on gene expression. While inhibitors of in vitro sumoylation exist, drugs that affect in vivo protein sumoylation have… (more)

Subjects/Keywords: Biochemistry; LRH-1; NR5A; Nuclear Receptor; SF-1; Sumoylation; Tannic Acid

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APA (6th Edition):

Gertz, K. R. (2014). Chemical and Genetic Regulation of Nuclear Receptor 5A (NR5A) Sumoylation. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/35j9s76j

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):

Gertz, Karmela Ramos. “Chemical and Genetic Regulation of Nuclear Receptor 5A (NR5A) Sumoylation.” 2014. Thesis, University of California – San Francisco. Accessed August 24, 2019. http://www.escholarship.org/uc/item/35j9s76j.

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

MLA Handbook (7th Edition):

Gertz, Karmela Ramos. “Chemical and Genetic Regulation of Nuclear Receptor 5A (NR5A) Sumoylation.” 2014. Web. 24 Aug 2019.

Vancouver:

Gertz KR. Chemical and Genetic Regulation of Nuclear Receptor 5A (NR5A) Sumoylation. [Internet] [Thesis]. University of California – San Francisco; 2014. [cited 2019 Aug 24]. Available from: http://www.escholarship.org/uc/item/35j9s76j.

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

Council of Science Editors:

Gertz KR. Chemical and Genetic Regulation of Nuclear Receptor 5A (NR5A) Sumoylation. [Thesis]. University of California – San Francisco; 2014. Available from: http://www.escholarship.org/uc/item/35j9s76j

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

21. Landgraf, Taise Natali. Receptor de aerobactina férrica de Escherichia coli - IutA: um novo antígeno T-independente do tipo 1.

Degree: Mestrado, Imunologia Básica e Aplicada, 2012, University of São Paulo

Alguns fatores de virulência em bactérias de microbiota normal, tais como sideróforos moléculas captadoras de ferro e determinadas fímbrias, possibilitam que esses microorganismos causem infecção… (more)

Subjects/Keywords: Ativação policlonal; B cells; Células B; IL-1 receptor; MyD88; MyD88; Polyclonal activation; Receptor de IL-1; Receptor de sideróforo; Siderophore receptor

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APA (6th Edition):

Landgraf, T. N. (2012). Receptor de aerobactina férrica de Escherichia coli - IutA: um novo antígeno T-independente do tipo 1. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/17/17147/tde-30072012-174116/ ;

Chicago Manual of Style (16th Edition):

Landgraf, Taise Natali. “Receptor de aerobactina férrica de Escherichia coli - IutA: um novo antígeno T-independente do tipo 1.” 2012. Masters Thesis, University of São Paulo. Accessed August 24, 2019. http://www.teses.usp.br/teses/disponiveis/17/17147/tde-30072012-174116/ ;.

MLA Handbook (7th Edition):

Landgraf, Taise Natali. “Receptor de aerobactina férrica de Escherichia coli - IutA: um novo antígeno T-independente do tipo 1.” 2012. Web. 24 Aug 2019.

Vancouver:

Landgraf TN. Receptor de aerobactina férrica de Escherichia coli - IutA: um novo antígeno T-independente do tipo 1. [Internet] [Masters thesis]. University of São Paulo; 2012. [cited 2019 Aug 24]. Available from: http://www.teses.usp.br/teses/disponiveis/17/17147/tde-30072012-174116/ ;.

Council of Science Editors:

Landgraf TN. Receptor de aerobactina férrica de Escherichia coli - IutA: um novo antígeno T-independente do tipo 1. [Masters Thesis]. University of São Paulo; 2012. Available from: http://www.teses.usp.br/teses/disponiveis/17/17147/tde-30072012-174116/ ;


Louisiana State University

22. Henagan, Tara Michelle. Exercise-induced alterations in melanocortin receptor expression and inflammation.

Degree: PhD, Kinesiology, 2010, Louisiana State University

  Inflammatory cytokines play a significant role in the pathogenesis of obesity-related diseases and have been implicated as integral factors in both early and late… (more)

Subjects/Keywords: exercise; resistance training; melanocortin 3 receptor; melanocortin 1 receptor; inflammation; macrophage; monocyte

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APA (6th Edition):

Henagan, T. M. (2010). Exercise-induced alterations in melanocortin receptor expression and inflammation. (Doctoral Dissertation). Louisiana State University. Retrieved from etd-08302010-202253 ; https://digitalcommons.lsu.edu/gradschool_dissertations/1018

Chicago Manual of Style (16th Edition):

Henagan, Tara Michelle. “Exercise-induced alterations in melanocortin receptor expression and inflammation.” 2010. Doctoral Dissertation, Louisiana State University. Accessed August 24, 2019. etd-08302010-202253 ; https://digitalcommons.lsu.edu/gradschool_dissertations/1018.

MLA Handbook (7th Edition):

Henagan, Tara Michelle. “Exercise-induced alterations in melanocortin receptor expression and inflammation.” 2010. Web. 24 Aug 2019.

Vancouver:

Henagan TM. Exercise-induced alterations in melanocortin receptor expression and inflammation. [Internet] [Doctoral dissertation]. Louisiana State University; 2010. [cited 2019 Aug 24]. Available from: etd-08302010-202253 ; https://digitalcommons.lsu.edu/gradschool_dissertations/1018.

Council of Science Editors:

Henagan TM. Exercise-induced alterations in melanocortin receptor expression and inflammation. [Doctoral Dissertation]. Louisiana State University; 2010. Available from: etd-08302010-202253 ; https://digitalcommons.lsu.edu/gradschool_dissertations/1018


University of Melbourne

23. Bumbak, Fabian. Characterising the conformational diversity of the neurotensin receptor 1.

Degree: 2016, University of Melbourne

 G Protein-Coupled Receptors (GPCRs) deliver approximately 80% of all signals across the cell membrane and are targets for around 26% of all prescription drugs. Conversely,… (more)

Subjects/Keywords: membrane proteins; GPCR; peptide receptor; neurotensin receptor 1; ligand binding; conformational dynamics; NMR; MD

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APA (6th Edition):

Bumbak, F. (2016). Characterising the conformational diversity of the neurotensin receptor 1. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/124282

Chicago Manual of Style (16th Edition):

Bumbak, Fabian. “Characterising the conformational diversity of the neurotensin receptor 1.” 2016. Doctoral Dissertation, University of Melbourne. Accessed August 24, 2019. http://hdl.handle.net/11343/124282.

MLA Handbook (7th Edition):

Bumbak, Fabian. “Characterising the conformational diversity of the neurotensin receptor 1.” 2016. Web. 24 Aug 2019.

Vancouver:

Bumbak F. Characterising the conformational diversity of the neurotensin receptor 1. [Internet] [Doctoral dissertation]. University of Melbourne; 2016. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/11343/124282.

Council of Science Editors:

Bumbak F. Characterising the conformational diversity of the neurotensin receptor 1. [Doctoral Dissertation]. University of Melbourne; 2016. Available from: http://hdl.handle.net/11343/124282


University of Arizona

24. 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 August 24, 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. 24 Aug 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 Aug 24]. 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 Toronto

25. Vincent, Lachlan MacLean Matthew. Ligands of the Elastin Receptor Stimulate Elastogenesis through cross-activation of the IGF-1 Signaling Pathway.

Degree: 2014, University of Toronto

It has been previously established that elastin degradation products can interact with the elastin receptor to induce elastogenesis. To elucidate this, we investigated the elastogenic… (more)

Subjects/Keywords: Dermal Fibroblasts; Elastin-like peptides; Elastin Receptor; IGF-1 Receptor; Regenerative Medicine; 0379

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APA (6th Edition):

Vincent, L. M. M. (2014). Ligands of the Elastin Receptor Stimulate Elastogenesis through cross-activation of the IGF-1 Signaling Pathway. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/68068

Chicago Manual of Style (16th Edition):

Vincent, Lachlan MacLean Matthew. “Ligands of the Elastin Receptor Stimulate Elastogenesis through cross-activation of the IGF-1 Signaling Pathway.” 2014. Masters Thesis, University of Toronto. Accessed August 24, 2019. http://hdl.handle.net/1807/68068.

MLA Handbook (7th Edition):

Vincent, Lachlan MacLean Matthew. “Ligands of the Elastin Receptor Stimulate Elastogenesis through cross-activation of the IGF-1 Signaling Pathway.” 2014. Web. 24 Aug 2019.

Vancouver:

Vincent LMM. Ligands of the Elastin Receptor Stimulate Elastogenesis through cross-activation of the IGF-1 Signaling Pathway. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1807/68068.

Council of Science Editors:

Vincent LMM. Ligands of the Elastin Receptor Stimulate Elastogenesis through cross-activation of the IGF-1 Signaling Pathway. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/68068


University of Rochester

26. Pallo, Susanne Pritchard. The Role of Tau and Amyloid-Beta in Alzheimer’s Disease-Related Mitochondrial Dysfunction and Excitotoxicity.

Degree: PhD, 2015, University of Rochester

 Alzheimer’s disease (AD) is mediated by abnormally processed tau and amyloid beta peptide (Aβ), which are proposed to act in concert to elicit mitochondria dysfunction… (more)

Subjects/Keywords: Kainate; Kainic Acid; Kainic Acid Receptor; Group 1 Metabotropic Glutamate Receptor; MGluR1; mGluR5

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APA (6th Edition):

Pallo, S. P. (2015). The Role of Tau and Amyloid-Beta in Alzheimer’s Disease-Related Mitochondrial Dysfunction and Excitotoxicity. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/30123

Chicago Manual of Style (16th Edition):

Pallo, Susanne Pritchard. “The Role of Tau and Amyloid-Beta in Alzheimer’s Disease-Related Mitochondrial Dysfunction and Excitotoxicity.” 2015. Doctoral Dissertation, University of Rochester. Accessed August 24, 2019. http://hdl.handle.net/1802/30123.

MLA Handbook (7th Edition):

Pallo, Susanne Pritchard. “The Role of Tau and Amyloid-Beta in Alzheimer’s Disease-Related Mitochondrial Dysfunction and Excitotoxicity.” 2015. Web. 24 Aug 2019.

Vancouver:

Pallo SP. The Role of Tau and Amyloid-Beta in Alzheimer’s Disease-Related Mitochondrial Dysfunction and Excitotoxicity. [Internet] [Doctoral dissertation]. University of Rochester; 2015. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/1802/30123.

Council of Science Editors:

Pallo SP. The Role of Tau and Amyloid-Beta in Alzheimer’s Disease-Related Mitochondrial Dysfunction and Excitotoxicity. [Doctoral Dissertation]. University of Rochester; 2015. Available from: http://hdl.handle.net/1802/30123


University of Minnesota

27. Kelley, Eli. The Effects Of Beta-1 And -2 Adrenergic Receptor Genotypes On Cardiopulmonary Outcomes In Duchenne Muscular Dystrophy.

Degree: PhD, Kinesiology, 2019, University of Minnesota

 Introduction: The main contributor of mortality in Duchenne muscular dystrophy (DMD) patients is cardiorespiratory failure. The beta-1 adrenergic receptor (ADRB1) has been shown to play… (more)

Subjects/Keywords: beta-1 adrenergic receptor; beta-2 adrenergic receptor; cardiomyopathy; Duchenne muscular dystrophy; nocturnal ventilation; respiratory

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APA (6th Edition):

Kelley, E. (2019). The Effects Of Beta-1 And -2 Adrenergic Receptor Genotypes On Cardiopulmonary Outcomes In Duchenne Muscular Dystrophy. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/206251

Chicago Manual of Style (16th Edition):

Kelley, Eli. “The Effects Of Beta-1 And -2 Adrenergic Receptor Genotypes On Cardiopulmonary Outcomes In Duchenne Muscular Dystrophy.” 2019. Doctoral Dissertation, University of Minnesota. Accessed August 24, 2019. http://hdl.handle.net/11299/206251.

MLA Handbook (7th Edition):

Kelley, Eli. “The Effects Of Beta-1 And -2 Adrenergic Receptor Genotypes On Cardiopulmonary Outcomes In Duchenne Muscular Dystrophy.” 2019. Web. 24 Aug 2019.

Vancouver:

Kelley E. The Effects Of Beta-1 And -2 Adrenergic Receptor Genotypes On Cardiopulmonary Outcomes In Duchenne Muscular Dystrophy. [Internet] [Doctoral dissertation]. University of Minnesota; 2019. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/11299/206251.

Council of Science Editors:

Kelley E. The Effects Of Beta-1 And -2 Adrenergic Receptor Genotypes On Cardiopulmonary Outcomes In Duchenne Muscular Dystrophy. [Doctoral Dissertation]. University of Minnesota; 2019. Available from: http://hdl.handle.net/11299/206251


University College Cork

28. Tetzner, Anja. Discovery and pharmacological characterisation of angiotensin-(1-7) receptors and identification of their importance in diabetes mellitus.

Degree: 2018, University College Cork

 The renin-angiotensin system (RAS) is known to be the main regulator of blood pressure and fluid balance. Within the RAS, angiotensin (Ang)-(1-7) is known to… (more)

Subjects/Keywords: Renin-angiotensin System; Angiotensin-(1-7); Mas receptor; MrgD receptor; AT2 receptor; G-proteins; Ala1-Angiotensin-(1-7); C21; Ang-(1-7)/Mas axis; Dose-response curve; Diabetes mellitus

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APA (6th Edition):

Tetzner, A. (2018). Discovery and pharmacological characterisation of angiotensin-(1-7) receptors and identification of their importance in diabetes mellitus. (Thesis). University College Cork. Retrieved from http://hdl.handle.net/10468/7333

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):

Tetzner, Anja. “Discovery and pharmacological characterisation of angiotensin-(1-7) receptors and identification of their importance in diabetes mellitus.” 2018. Thesis, University College Cork. Accessed August 24, 2019. http://hdl.handle.net/10468/7333.

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

MLA Handbook (7th Edition):

Tetzner, Anja. “Discovery and pharmacological characterisation of angiotensin-(1-7) receptors and identification of their importance in diabetes mellitus.” 2018. Web. 24 Aug 2019.

Vancouver:

Tetzner A. Discovery and pharmacological characterisation of angiotensin-(1-7) receptors and identification of their importance in diabetes mellitus. [Internet] [Thesis]. University College Cork; 2018. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/10468/7333.

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

Council of Science Editors:

Tetzner A. Discovery and pharmacological characterisation of angiotensin-(1-7) receptors and identification of their importance in diabetes mellitus. [Thesis]. University College Cork; 2018. Available from: http://hdl.handle.net/10468/7333

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

29. Davis, Perry Victoria. Evaluating the Interaction Between the Human Mealanocortin-2 Receptor and the Accessory Protein, Mrap1: Chimeric Receptor and Alanine Substitution Studies on Transmembrane Domain 4, Extracellular Loop 2, and Transmembrane Domain 5.

Degree: PhD, Biological Sciences, 2018, U of Denver

  The melanocortin-2 receptor (MC2R) is the most complex due to its trafficking and ligand selectivity requirements for proper activation. The MC2R requires the melanocortin… (more)

Subjects/Keywords: Alanine substitution; Chimeric receptor; MC2R; Melanocortin-2 receptor; Melanocortin receptor accessory protein 1; MRAP1; Biochemistry; Cell Biology

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APA (6th Edition):

Davis, P. V. (2018). Evaluating the Interaction Between the Human Mealanocortin-2 Receptor and the Accessory Protein, Mrap1: Chimeric Receptor and Alanine Substitution Studies on Transmembrane Domain 4, Extracellular Loop 2, and Transmembrane Domain 5. (Doctoral Dissertation). U of Denver. Retrieved from https://digitalcommons.du.edu/etd/1530

Chicago Manual of Style (16th Edition):

Davis, Perry Victoria. “Evaluating the Interaction Between the Human Mealanocortin-2 Receptor and the Accessory Protein, Mrap1: Chimeric Receptor and Alanine Substitution Studies on Transmembrane Domain 4, Extracellular Loop 2, and Transmembrane Domain 5.” 2018. Doctoral Dissertation, U of Denver. Accessed August 24, 2019. https://digitalcommons.du.edu/etd/1530.

MLA Handbook (7th Edition):

Davis, Perry Victoria. “Evaluating the Interaction Between the Human Mealanocortin-2 Receptor and the Accessory Protein, Mrap1: Chimeric Receptor and Alanine Substitution Studies on Transmembrane Domain 4, Extracellular Loop 2, and Transmembrane Domain 5.” 2018. Web. 24 Aug 2019.

Vancouver:

Davis PV. Evaluating the Interaction Between the Human Mealanocortin-2 Receptor and the Accessory Protein, Mrap1: Chimeric Receptor and Alanine Substitution Studies on Transmembrane Domain 4, Extracellular Loop 2, and Transmembrane Domain 5. [Internet] [Doctoral dissertation]. U of Denver; 2018. [cited 2019 Aug 24]. Available from: https://digitalcommons.du.edu/etd/1530.

Council of Science Editors:

Davis PV. Evaluating the Interaction Between the Human Mealanocortin-2 Receptor and the Accessory Protein, Mrap1: Chimeric Receptor and Alanine Substitution Studies on Transmembrane Domain 4, Extracellular Loop 2, and Transmembrane Domain 5. [Doctoral Dissertation]. U of Denver; 2018. Available from: https://digitalcommons.du.edu/etd/1530

30. Carvalho, João Henrique de. Análise da expressão e atividade de receptores ativados por proteases em plaquetas de pacientes com hipertensão arterial pulmonar.

Degree: Mestrado, Fisiopatologia Experimental, 2009, University of São Paulo

A hipertensão arterial pulmonar é uma síndrome clínica e hemodinâmica, caracterizada pelo aumento de resistência vascular na microcirculação. A vasoconstrição presente na doença ocorre principalmente… (more)

Subjects/Keywords: Hipertensão pulmonar; P-Selectin; Plaquetas; Platelets; Protease activated receptor 1/antagonists; Pulmonary hypertension; Receptor PAR-1/Antagonistas; Selectina-P; Thrombosis; Trombose

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APA (6th Edition):

Carvalho, J. H. d. (2009). Análise da expressão e atividade de receptores ativados por proteases em plaquetas de pacientes com hipertensão arterial pulmonar. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5160/tde-01062009-114009/ ;

Chicago Manual of Style (16th Edition):

Carvalho, João Henrique de. “Análise da expressão e atividade de receptores ativados por proteases em plaquetas de pacientes com hipertensão arterial pulmonar.” 2009. Masters Thesis, University of São Paulo. Accessed August 24, 2019. http://www.teses.usp.br/teses/disponiveis/5/5160/tde-01062009-114009/ ;.

MLA Handbook (7th Edition):

Carvalho, João Henrique de. “Análise da expressão e atividade de receptores ativados por proteases em plaquetas de pacientes com hipertensão arterial pulmonar.” 2009. Web. 24 Aug 2019.

Vancouver:

Carvalho JHd. Análise da expressão e atividade de receptores ativados por proteases em plaquetas de pacientes com hipertensão arterial pulmonar. [Internet] [Masters thesis]. University of São Paulo; 2009. [cited 2019 Aug 24]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-01062009-114009/ ;.

Council of Science Editors:

Carvalho JHd. Análise da expressão e atividade de receptores ativados por proteases em plaquetas de pacientes com hipertensão arterial pulmonar. [Masters Thesis]. University of São Paulo; 2009. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-01062009-114009/ ;

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