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You searched for subject:(Nuclear receptors Biochemistry ). Showing records 1 – 30 of 36548 total matches.

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1. Noto, Paul Bart. Analysis of Liver X Receptor target gene expression across species.

Degree: 2013, Drexel University

Liver X Receptors (LXRs) are nuclear hormone receptors that regulate key genes involved in cholesterol and lipid metabolism. As transcription factors, LXRs turn on the… (more)

Subjects/Keywords: Biological Sciences; Nuclear receptors (Biochemistry); Pharmacology

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

APA (6th Edition):

Noto, P. B. (2013). Analysis of Liver X Receptor target gene expression across species. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/4198

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):

Noto, Paul Bart. “Analysis of Liver X Receptor target gene expression across species.” 2013. Thesis, Drexel University. Accessed November 27, 2020. http://hdl.handle.net/1860/4198.

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

MLA Handbook (7th Edition):

Noto, Paul Bart. “Analysis of Liver X Receptor target gene expression across species.” 2013. Web. 27 Nov 2020.

Vancouver:

Noto PB. Analysis of Liver X Receptor target gene expression across species. [Internet] [Thesis]. Drexel University; 2013. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1860/4198.

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

Council of Science Editors:

Noto PB. Analysis of Liver X Receptor target gene expression across species. [Thesis]. Drexel University; 2013. Available from: http://hdl.handle.net/1860/4198

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


Oregon State University

2. Yang, Liping. Effects of small molecule ligands on the conformational dynamics of the Farnesoid X Receptor ligand binding domain (FXR-LBD).

Degree: PhD, Chemistry, 2014, Oregon State University

 The Farnesoid X Receptor (FXR) is a member of the nuclear receptor superfamily of transcription factors that plays a key role in the regulation of… (more)

Subjects/Keywords: Farnesoid X Receptor; Nuclear receptors (Biochemistry)

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APA (6th Edition):

Yang, L. (2014). Effects of small molecule ligands on the conformational dynamics of the Farnesoid X Receptor ligand binding domain (FXR-LBD). (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/49982

Chicago Manual of Style (16th Edition):

Yang, Liping. “Effects of small molecule ligands on the conformational dynamics of the Farnesoid X Receptor ligand binding domain (FXR-LBD).” 2014. Doctoral Dissertation, Oregon State University. Accessed November 27, 2020. http://hdl.handle.net/1957/49982.

MLA Handbook (7th Edition):

Yang, Liping. “Effects of small molecule ligands on the conformational dynamics of the Farnesoid X Receptor ligand binding domain (FXR-LBD).” 2014. Web. 27 Nov 2020.

Vancouver:

Yang L. Effects of small molecule ligands on the conformational dynamics of the Farnesoid X Receptor ligand binding domain (FXR-LBD). [Internet] [Doctoral dissertation]. Oregon State University; 2014. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1957/49982.

Council of Science Editors:

Yang L. Effects of small molecule ligands on the conformational dynamics of the Farnesoid X Receptor ligand binding domain (FXR-LBD). [Doctoral Dissertation]. Oregon State University; 2014. Available from: http://hdl.handle.net/1957/49982


Columbia University

3. Thomas, David George. Liver X Receptor cis-Repression and Cholesterol Efflux Restrain Innate Immunity and Coronary Artery Disease.

Degree: 2019, Columbia University

 Atherosclerotic cardiovascular disease secondary to deposition of apolipoprotein B-containing lipoproteins in the artery wall is a leading cause of mortality. Therapies that reduce serum levels… (more)

Subjects/Keywords: Cytology; Molecular biology; Biochemistry; Atherosclerosis – Prevention; Immunity; Nuclear receptors (Biochemistry)

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APA (6th Edition):

Thomas, D. G. (2019). Liver X Receptor cis-Repression and Cholesterol Efflux Restrain Innate Immunity and Coronary Artery Disease. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/d8-5wc2-4f04

Chicago Manual of Style (16th Edition):

Thomas, David George. “Liver X Receptor cis-Repression and Cholesterol Efflux Restrain Innate Immunity and Coronary Artery Disease.” 2019. Doctoral Dissertation, Columbia University. Accessed November 27, 2020. https://doi.org/10.7916/d8-5wc2-4f04.

MLA Handbook (7th Edition):

Thomas, David George. “Liver X Receptor cis-Repression and Cholesterol Efflux Restrain Innate Immunity and Coronary Artery Disease.” 2019. Web. 27 Nov 2020.

Vancouver:

Thomas DG. Liver X Receptor cis-Repression and Cholesterol Efflux Restrain Innate Immunity and Coronary Artery Disease. [Internet] [Doctoral dissertation]. Columbia University; 2019. [cited 2020 Nov 27]. Available from: https://doi.org/10.7916/d8-5wc2-4f04.

Council of Science Editors:

Thomas DG. Liver X Receptor cis-Repression and Cholesterol Efflux Restrain Innate Immunity and Coronary Artery Disease. [Doctoral Dissertation]. Columbia University; 2019. Available from: https://doi.org/10.7916/d8-5wc2-4f04


Texas Tech University

4. Boston, William Lee. Characterization of clone D2: An orphan protein that interacts with peroxisome proliferator-activated receptor gamma.

Degree: TTUHSC  – Immunology and Infectious Diseases, 2002, Texas Tech University

 Phosphoenolpymvate carboxykinase (PEPCK) expression is regulated in a tissue specific manner. However, understanding the expression pattern in different tissues is not well documented. We are… (more)

Subjects/Keywords: Antioncogenes; Peroxisomes; Nuclear receptors (Biochemistry)

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APA (6th Edition):

Boston, W. L. (2002). Characterization of clone D2: An orphan protein that interacts with peroxisome proliferator-activated receptor gamma. (Thesis). Texas Tech University. Retrieved from http://hdl.handle.net/2346/15112

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):

Boston, William Lee. “Characterization of clone D2: An orphan protein that interacts with peroxisome proliferator-activated receptor gamma.” 2002. Thesis, Texas Tech University. Accessed November 27, 2020. http://hdl.handle.net/2346/15112.

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

MLA Handbook (7th Edition):

Boston, William Lee. “Characterization of clone D2: An orphan protein that interacts with peroxisome proliferator-activated receptor gamma.” 2002. Web. 27 Nov 2020.

Vancouver:

Boston WL. Characterization of clone D2: An orphan protein that interacts with peroxisome proliferator-activated receptor gamma. [Internet] [Thesis]. Texas Tech University; 2002. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2346/15112.

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

Council of Science Editors:

Boston WL. Characterization of clone D2: An orphan protein that interacts with peroxisome proliferator-activated receptor gamma. [Thesis]. Texas Tech University; 2002. Available from: http://hdl.handle.net/2346/15112

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


Northeastern University

5. Williams, Anna B. Synthesis & evaluation of bipolar biphenyl proteomimetics as nuclear receptor CBIs and applications of palladium chemistry to the development of radiotracers; Synthesis and evaluation of bipolar biphenyl proteomimetics as nuclear receptor CBIs and applications of palladium chemistry to the development of radiotracers.

Degree: PhD, Department of Chemistry and Chemical Biology, 2011, Northeastern University

 Protein-protein interactions (PPIs) are essential activation and communication mechanisms for countless biological processes. The ability to inhibit PPIs therefore exposes therapeutic pathways for ailments that… (more)

Subjects/Keywords: organic chemistry; chemistry; alpha helix mimetics; biphenyl; nuclear receptor; palladium catalysis; proteomimetics; radiotracer; Protein-protein interactions; Nuclear receptors (Biochemistry); Biochemistry

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APA (6th Edition):

Williams, A. B. (2011). Synthesis & evaluation of bipolar biphenyl proteomimetics as nuclear receptor CBIs and applications of palladium chemistry to the development of radiotracers; Synthesis and evaluation of bipolar biphenyl proteomimetics as nuclear receptor CBIs and applications of palladium chemistry to the development of radiotracers. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20001221

Chicago Manual of Style (16th Edition):

Williams, Anna B. “Synthesis & evaluation of bipolar biphenyl proteomimetics as nuclear receptor CBIs and applications of palladium chemistry to the development of radiotracers; Synthesis and evaluation of bipolar biphenyl proteomimetics as nuclear receptor CBIs and applications of palladium chemistry to the development of radiotracers.” 2011. Doctoral Dissertation, Northeastern University. Accessed November 27, 2020. http://hdl.handle.net/2047/d20001221.

MLA Handbook (7th Edition):

Williams, Anna B. “Synthesis & evaluation of bipolar biphenyl proteomimetics as nuclear receptor CBIs and applications of palladium chemistry to the development of radiotracers; Synthesis and evaluation of bipolar biphenyl proteomimetics as nuclear receptor CBIs and applications of palladium chemistry to the development of radiotracers.” 2011. Web. 27 Nov 2020.

Vancouver:

Williams AB. Synthesis & evaluation of bipolar biphenyl proteomimetics as nuclear receptor CBIs and applications of palladium chemistry to the development of radiotracers; Synthesis and evaluation of bipolar biphenyl proteomimetics as nuclear receptor CBIs and applications of palladium chemistry to the development of radiotracers. [Internet] [Doctoral dissertation]. Northeastern University; 2011. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2047/d20001221.

Council of Science Editors:

Williams AB. Synthesis & evaluation of bipolar biphenyl proteomimetics as nuclear receptor CBIs and applications of palladium chemistry to the development of radiotracers; Synthesis and evaluation of bipolar biphenyl proteomimetics as nuclear receptor CBIs and applications of palladium chemistry to the development of radiotracers. [Doctoral Dissertation]. Northeastern University; 2011. Available from: http://hdl.handle.net/2047/d20001221


University of Hong Kong

6. Cheng, Wai. The relationship between peroxisome proliferator-activated receptors (PPARs) and cell proliferation.

Degree: 2006, University of Hong Kong

Subjects/Keywords: Nuclear receptors (Biochemistry); Transcription factors.; Peroxisomes - Receptors.; Cell proliferation.

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APA (6th Edition):

Cheng, W. (2006). The relationship between peroxisome proliferator-activated receptors (PPARs) and cell proliferation. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/131229

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):

Cheng, Wai. “The relationship between peroxisome proliferator-activated receptors (PPARs) and cell proliferation.” 2006. Thesis, University of Hong Kong. Accessed November 27, 2020. http://hdl.handle.net/10722/131229.

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

MLA Handbook (7th Edition):

Cheng, Wai. “The relationship between peroxisome proliferator-activated receptors (PPARs) and cell proliferation.” 2006. Web. 27 Nov 2020.

Vancouver:

Cheng W. The relationship between peroxisome proliferator-activated receptors (PPARs) and cell proliferation. [Internet] [Thesis]. University of Hong Kong; 2006. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10722/131229.

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

Council of Science Editors:

Cheng W. The relationship between peroxisome proliferator-activated receptors (PPARs) and cell proliferation. [Thesis]. University of Hong Kong; 2006. Available from: http://hdl.handle.net/10722/131229

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

7. Kim, Jung-Hwan. Investigation of novel NRF2 partners, RAC3 and IQGAP1.

Degree: PhD, Pharmaceutical Science, 2009, Rutgers University

Nuclear factor-erythroid-related factor 2 (Nrf2) is essential for the antioxidant responsive element (ARE)-mediated expression of a group of detoxifying and antioxidant genes, which detoxify carcinogens… (more)

Subjects/Keywords: Transcription factors; Cell receptors; Nuclear receptors (Biochemistry)

…ABBREVIATIONS Nrf2, Nuclear factor-erythroid 2-related factor 2 RAC-3, Receptor-associated coactivator… …3 NCoA-3, Nuclear receptor coactivator 3 TRAM-1, Thyroid hormone receptor activator… …molecule 1 ACTR, Activator of retinoid and thyroid receptors pCIP, CBP-interacting protein. Neh… …regulated by the nuclear factor-erythroid 2-related factor 2 (Nrf2)(95, 119, 168… …with other transcription factors. In addition, a functional NLS (nuclear localization… 

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APA (6th Edition):

Kim, J. (2009). Investigation of novel NRF2 partners, RAC3 and IQGAP1. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052254

Chicago Manual of Style (16th Edition):

Kim, Jung-Hwan. “Investigation of novel NRF2 partners, RAC3 and IQGAP1.” 2009. Doctoral Dissertation, Rutgers University. Accessed November 27, 2020. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052254.

MLA Handbook (7th Edition):

Kim, Jung-Hwan. “Investigation of novel NRF2 partners, RAC3 and IQGAP1.” 2009. Web. 27 Nov 2020.

Vancouver:

Kim J. Investigation of novel NRF2 partners, RAC3 and IQGAP1. [Internet] [Doctoral dissertation]. Rutgers University; 2009. [cited 2020 Nov 27]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052254.

Council of Science Editors:

Kim J. Investigation of novel NRF2 partners, RAC3 and IQGAP1. [Doctoral Dissertation]. Rutgers University; 2009. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052254


University of Delaware

8. Cruz, Federico Guillermo. Light-activated gene expression.

Degree: PhD, University of Delaware, Department of Chemistry and Biochemistry, 2016, University of Delaware

 A method for activating gene expression in cells by using photo-caged small molecules was developed. This method uses the Nuclear Hormone Receptor (NHR) family as… (more)

Subjects/Keywords: Ultraviolet radiation.; Activation (Chemistry); Gene expression.; Nuclear receptors (Biochemistry); Receptor-ligand complexes.; Molecules.

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APA (6th Edition):

Cruz, F. G. (2016). Light-activated gene expression. (Doctoral Dissertation). University of Delaware. Retrieved from http://udspace.udel.edu/handle/19716/21491

Chicago Manual of Style (16th Edition):

Cruz, Federico Guillermo. “Light-activated gene expression.” 2016. Doctoral Dissertation, University of Delaware. Accessed November 27, 2020. http://udspace.udel.edu/handle/19716/21491.

MLA Handbook (7th Edition):

Cruz, Federico Guillermo. “Light-activated gene expression.” 2016. Web. 27 Nov 2020.

Vancouver:

Cruz FG. Light-activated gene expression. [Internet] [Doctoral dissertation]. University of Delaware; 2016. [cited 2020 Nov 27]. Available from: http://udspace.udel.edu/handle/19716/21491.

Council of Science Editors:

Cruz FG. Light-activated gene expression. [Doctoral Dissertation]. University of Delaware; 2016. Available from: http://udspace.udel.edu/handle/19716/21491


University of Hong Kong

9. 屈晨. The dual peroxisome proliferator-activated receptor α/[gamma] agonist Wy14643 improves endothelial function in the aorta of thespontaneously hypertensive rat.

Degree: 2011, University of Hong Kong

Subjects/Keywords: Aorta.; Vascular endothelium.; Nuclear receptors (Biochemistry)

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APA (6th Edition):

屈晨. (2011). The dual peroxisome proliferator-activated receptor α/[gamma] agonist Wy14643 improves endothelial function in the aorta of thespontaneously hypertensive rat. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/144154

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

Chicago Manual of Style (16th Edition):

屈晨. “The dual peroxisome proliferator-activated receptor α/[gamma] agonist Wy14643 improves endothelial function in the aorta of thespontaneously hypertensive rat.” 2011. Thesis, University of Hong Kong. Accessed November 27, 2020. http://hdl.handle.net/10722/144154.

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

MLA Handbook (7th Edition):

屈晨. “The dual peroxisome proliferator-activated receptor α/[gamma] agonist Wy14643 improves endothelial function in the aorta of thespontaneously hypertensive rat.” 2011. Web. 27 Nov 2020.

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

Vancouver:

屈晨. The dual peroxisome proliferator-activated receptor α/[gamma] agonist Wy14643 improves endothelial function in the aorta of thespontaneously hypertensive rat. [Internet] [Thesis]. University of Hong Kong; 2011. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10722/144154.

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

Council of Science Editors:

屈晨. The dual peroxisome proliferator-activated receptor α/[gamma] agonist Wy14643 improves endothelial function in the aorta of thespontaneously hypertensive rat. [Thesis]. University of Hong Kong; 2011. Available from: http://hdl.handle.net/10722/144154

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


IUPUI

10. Martel, Kellie Clay. THE PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR γ ANTAGONIST, GW9662, ALTERS UVB-INDUCED INFLAMMATORY RESPONSES, APOPTOSIS, AND DELAYED HYPERPROLIFERATION.

Degree: 2008, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

It has recently been shown that the gamma subtype of the peroxisome proliferator-activated receptor (PPARγ) is a target of ultraviolet… (more)

Subjects/Keywords: PPARγ; UVB; COX-2; Nuclear receptors (Biochemistry)

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APA (6th Edition):

Martel, K. C. (2008). THE PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR γ ANTAGONIST, GW9662, ALTERS UVB-INDUCED INFLAMMATORY RESPONSES, APOPTOSIS, AND DELAYED HYPERPROLIFERATION. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/1727

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):

Martel, Kellie Clay. “THE PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR γ ANTAGONIST, GW9662, ALTERS UVB-INDUCED INFLAMMATORY RESPONSES, APOPTOSIS, AND DELAYED HYPERPROLIFERATION.” 2008. Thesis, IUPUI. Accessed November 27, 2020. http://hdl.handle.net/1805/1727.

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

MLA Handbook (7th Edition):

Martel, Kellie Clay. “THE PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR γ ANTAGONIST, GW9662, ALTERS UVB-INDUCED INFLAMMATORY RESPONSES, APOPTOSIS, AND DELAYED HYPERPROLIFERATION.” 2008. Web. 27 Nov 2020.

Vancouver:

Martel KC. THE PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR γ ANTAGONIST, GW9662, ALTERS UVB-INDUCED INFLAMMATORY RESPONSES, APOPTOSIS, AND DELAYED HYPERPROLIFERATION. [Internet] [Thesis]. IUPUI; 2008. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1805/1727.

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

Council of Science Editors:

Martel KC. THE PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR γ ANTAGONIST, GW9662, ALTERS UVB-INDUCED INFLAMMATORY RESPONSES, APOPTOSIS, AND DELAYED HYPERPROLIFERATION. [Thesis]. IUPUI; 2008. Available from: http://hdl.handle.net/1805/1727

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


University of Hong Kong

11. 蔡綺. The possible mechanisms of peroxisome proliferator-activatedreceptor (PPAR) agonists in controlling graft rejection.

Degree: 2005, University of Hong Kong

Subjects/Keywords: Hypoglycemic agents.; Graft rejection - Prevention.; Transcription factors.; Peroxisomes - Receptors.; Nuclear receptors (Biochemistry)

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APA (6th Edition):

蔡綺. (2005). The possible mechanisms of peroxisome proliferator-activatedreceptor (PPAR) agonists in controlling graft rejection. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/52783

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

Chicago Manual of Style (16th Edition):

蔡綺. “The possible mechanisms of peroxisome proliferator-activatedreceptor (PPAR) agonists in controlling graft rejection.” 2005. Thesis, University of Hong Kong. Accessed November 27, 2020. http://hdl.handle.net/10722/52783.

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

MLA Handbook (7th Edition):

蔡綺. “The possible mechanisms of peroxisome proliferator-activatedreceptor (PPAR) agonists in controlling graft rejection.” 2005. Web. 27 Nov 2020.

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

Vancouver:

蔡綺. The possible mechanisms of peroxisome proliferator-activatedreceptor (PPAR) agonists in controlling graft rejection. [Internet] [Thesis]. University of Hong Kong; 2005. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10722/52783.

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

Council of Science Editors:

蔡綺. The possible mechanisms of peroxisome proliferator-activatedreceptor (PPAR) agonists in controlling graft rejection. [Thesis]. University of Hong Kong; 2005. Available from: http://hdl.handle.net/10722/52783

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


University of Hong Kong

12. 浦愷文. Expression of peroxisome proliferator-activated receptors is affected by metabolic state and bitter melon (Momordica charantia)supplementation.

Degree: 2006, University of Hong Kong

Subjects/Keywords: Nuclear receptors (Biochemistry); Peroxisomes - Receptors.; Gene expression.; Rats - Physiology.; Momordica charantia.; Transcription factors.

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APA (6th Edition):

浦愷文.. (2006). Expression of peroxisome proliferator-activated receptors is affected by metabolic state and bitter melon (Momordica charantia)supplementation. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/52849

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

Chicago Manual of Style (16th Edition):

浦愷文.. “Expression of peroxisome proliferator-activated receptors is affected by metabolic state and bitter melon (Momordica charantia)supplementation.” 2006. Thesis, University of Hong Kong. Accessed November 27, 2020. http://hdl.handle.net/10722/52849.

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

MLA Handbook (7th Edition):

浦愷文.. “Expression of peroxisome proliferator-activated receptors is affected by metabolic state and bitter melon (Momordica charantia)supplementation.” 2006. Web. 27 Nov 2020.

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

Vancouver:

浦愷文.. Expression of peroxisome proliferator-activated receptors is affected by metabolic state and bitter melon (Momordica charantia)supplementation. [Internet] [Thesis]. University of Hong Kong; 2006. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10722/52849.

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

Council of Science Editors:

浦愷文.. Expression of peroxisome proliferator-activated receptors is affected by metabolic state and bitter melon (Momordica charantia)supplementation. [Thesis]. University of Hong Kong; 2006. Available from: http://hdl.handle.net/10722/52849

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


Universitat de Barcelona

13. Carbó Marqués, José Mª. Papel del receptor nuclear LXR en la proliferación y perfil metastático de células tumorales y en la actividad de macrófagos asociados a tumor.

Degree: Departament de Biologia Cel·lular, Fisiologia i Immunologia, 2017, Universitat de Barcelona

 Liver X receptors are ligand dependent transcription factors that participate in the cholesterol reverse transport, glucose metabolism and the modulation of the immune system. In… (more)

Subjects/Keywords: Metàstasi; Metástasis; Metastasis; Cèl·lules canceroses; Células cancerosas; Cancer cells; Receptors nuclears (Bioquímica); Receptores nucleares (Bioquímica); Nuclear receptors (Biochemistry); Macròfags; Macrófagos; Macrophages; Ciències Experimentals i Matemàtiques; 577

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APA (6th Edition):

Carbó Marqués, J. M. (2017). Papel del receptor nuclear LXR en la proliferación y perfil metastático de células tumorales y en la actividad de macrófagos asociados a tumor. (Thesis). Universitat de Barcelona. Retrieved from http://hdl.handle.net/10803/461986

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):

Carbó Marqués, José Mª. “Papel del receptor nuclear LXR en la proliferación y perfil metastático de células tumorales y en la actividad de macrófagos asociados a tumor.” 2017. Thesis, Universitat de Barcelona. Accessed November 27, 2020. http://hdl.handle.net/10803/461986.

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

MLA Handbook (7th Edition):

Carbó Marqués, José Mª. “Papel del receptor nuclear LXR en la proliferación y perfil metastático de células tumorales y en la actividad de macrófagos asociados a tumor.” 2017. Web. 27 Nov 2020.

Vancouver:

Carbó Marqués JM. Papel del receptor nuclear LXR en la proliferación y perfil metastático de células tumorales y en la actividad de macrófagos asociados a tumor. [Internet] [Thesis]. Universitat de Barcelona; 2017. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10803/461986.

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

Council of Science Editors:

Carbó Marqués JM. Papel del receptor nuclear LXR en la proliferación y perfil metastático de células tumorales y en la actividad de macrófagos asociados a tumor. [Thesis]. Universitat de Barcelona; 2017. Available from: http://hdl.handle.net/10803/461986

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


Universitat de Barcelona

14. Abad Morales, Víctor. SUMO a la retina: expressió gènica i rellevància en la modificació posttaducciontal del factor de transcripció NRE3.

Degree: Departament de Genètica, Microbiologia i Estadística, 2017, Universitat de Barcelona

 Sumoylation is a reversible post-translational modification that regulates different cellular processes by conjugation/deconjugation of SUMO moieties to target proteins. Most work on the functional relevance… (more)

Subjects/Keywords: Proteïnes; Proteínas; Proteins; Ubiqüitina; Ubicuitina; Ubiquitin; Receptors nuclears (Bioquímica); Receptores nucleares (Bioquímica); Nuclear receptors (Biochemistry); Expressió gènica; Expresión génica; Gene expression; Ciències Experimentals i Matemàtiques; 575

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APA (6th Edition):

Abad Morales, V. (2017). SUMO a la retina: expressió gènica i rellevància en la modificació posttaducciontal del factor de transcripció NRE3. (Thesis). Universitat de Barcelona. Retrieved from http://hdl.handle.net/10803/402783

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):

Abad Morales, Víctor. “SUMO a la retina: expressió gènica i rellevància en la modificació posttaducciontal del factor de transcripció NRE3.” 2017. Thesis, Universitat de Barcelona. Accessed November 27, 2020. http://hdl.handle.net/10803/402783.

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

MLA Handbook (7th Edition):

Abad Morales, Víctor. “SUMO a la retina: expressió gènica i rellevància en la modificació posttaducciontal del factor de transcripció NRE3.” 2017. Web. 27 Nov 2020.

Vancouver:

Abad Morales V. SUMO a la retina: expressió gènica i rellevància en la modificació posttaducciontal del factor de transcripció NRE3. [Internet] [Thesis]. Universitat de Barcelona; 2017. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10803/402783.

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

Council of Science Editors:

Abad Morales V. SUMO a la retina: expressió gènica i rellevància en la modificació posttaducciontal del factor de transcripció NRE3. [Thesis]. Universitat de Barcelona; 2017. Available from: http://hdl.handle.net/10803/402783

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


Universitat de Barcelona

15. Moran Salvador, Eva. Papel del receptor nuclear PPARgamma en la inflamación y la esteatosis hepática.

Degree: Departament de Ciències Fisiològiques I, 2013, Universitat de Barcelona

 PPARgamma plays an essential role in the transcriptional regulation of genes involved in lipid and glucose metabolism, insulin sensitivity and inflammation. In the project we… (more)

Subjects/Keywords: Inflamació; Inflamación; Inflammation; Receptors nuclears (Bioquímica); Receptores nucleares (Bioquímica); Nuclear receptors (Biochemistry); Malalties del fetge; Enfermedades del higado; Liver diseases; Ciències de la Salut; 612

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APA (6th Edition):

Moran Salvador, E. (2013). Papel del receptor nuclear PPARgamma en la inflamación y la esteatosis hepática. (Thesis). Universitat de Barcelona. Retrieved from http://hdl.handle.net/10803/293262

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):

Moran Salvador, Eva. “Papel del receptor nuclear PPARgamma en la inflamación y la esteatosis hepática.” 2013. Thesis, Universitat de Barcelona. Accessed November 27, 2020. http://hdl.handle.net/10803/293262.

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

MLA Handbook (7th Edition):

Moran Salvador, Eva. “Papel del receptor nuclear PPARgamma en la inflamación y la esteatosis hepática.” 2013. Web. 27 Nov 2020.

Vancouver:

Moran Salvador E. Papel del receptor nuclear PPARgamma en la inflamación y la esteatosis hepática. [Internet] [Thesis]. Universitat de Barcelona; 2013. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10803/293262.

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

Council of Science Editors:

Moran Salvador E. Papel del receptor nuclear PPARgamma en la inflamación y la esteatosis hepática. [Thesis]. Universitat de Barcelona; 2013. Available from: http://hdl.handle.net/10803/293262

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


East Carolina University

16. Daly, Sean. LOCALIZATION AND CHANGES OF NUCLEAR PROGESTERONE RECEPTORS IN ZEBRAFISH OOCYTES AND ADJACENT FOLLICULAR CELLS.

Degree: MS, Biology, 2010, East Carolina University

 The nuclear progesterone receptor (Pgr) is one of the major mediators for progestin signaling during oocyte ovulation in vertebrates. However, any roles Pgr may play… (more)

Subjects/Keywords: Biology, Molecular; Molecular biology; Progesterone – Receptors; Zebra danio – Eggs; Nuclear receptors (Biochemistry)

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APA (6th Edition):

Daly, S. (2010). LOCALIZATION AND CHANGES OF NUCLEAR PROGESTERONE RECEPTORS IN ZEBRAFISH OOCYTES AND ADJACENT FOLLICULAR CELLS. (Masters Thesis). East Carolina University. Retrieved from http://hdl.handle.net/10342/3145

Chicago Manual of Style (16th Edition):

Daly, Sean. “LOCALIZATION AND CHANGES OF NUCLEAR PROGESTERONE RECEPTORS IN ZEBRAFISH OOCYTES AND ADJACENT FOLLICULAR CELLS.” 2010. Masters Thesis, East Carolina University. Accessed November 27, 2020. http://hdl.handle.net/10342/3145.

MLA Handbook (7th Edition):

Daly, Sean. “LOCALIZATION AND CHANGES OF NUCLEAR PROGESTERONE RECEPTORS IN ZEBRAFISH OOCYTES AND ADJACENT FOLLICULAR CELLS.” 2010. Web. 27 Nov 2020.

Vancouver:

Daly S. LOCALIZATION AND CHANGES OF NUCLEAR PROGESTERONE RECEPTORS IN ZEBRAFISH OOCYTES AND ADJACENT FOLLICULAR CELLS. [Internet] [Masters thesis]. East Carolina University; 2010. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10342/3145.

Council of Science Editors:

Daly S. LOCALIZATION AND CHANGES OF NUCLEAR PROGESTERONE RECEPTORS IN ZEBRAFISH OOCYTES AND ADJACENT FOLLICULAR CELLS. [Masters Thesis]. East Carolina University; 2010. Available from: http://hdl.handle.net/10342/3145


Texas Tech University

17. Xia, Zhenfang. Cloning and characterization of the estrogen receptor of channel catfish.

Degree: 1998, Texas Tech University

Subjects/Keywords: Channel catfish  – Genetics; Estrogen  – Receptors  – Analysis; Cloning; Nuclear receptors (Biochemistry)

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APA (6th Edition):

Xia, Z. (1998). Cloning and characterization of the estrogen receptor of channel catfish. (Thesis). Texas Tech University. Retrieved from http://hdl.handle.net/2346/14008

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):

Xia, Zhenfang. “Cloning and characterization of the estrogen receptor of channel catfish.” 1998. Thesis, Texas Tech University. Accessed November 27, 2020. http://hdl.handle.net/2346/14008.

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

MLA Handbook (7th Edition):

Xia, Zhenfang. “Cloning and characterization of the estrogen receptor of channel catfish.” 1998. Web. 27 Nov 2020.

Vancouver:

Xia Z. Cloning and characterization of the estrogen receptor of channel catfish. [Internet] [Thesis]. Texas Tech University; 1998. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2346/14008.

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

Council of Science Editors:

Xia Z. Cloning and characterization of the estrogen receptor of channel catfish. [Thesis]. Texas Tech University; 1998. Available from: http://hdl.handle.net/2346/14008

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

18. Heskett, Michael B. Epigenetic Regulation of Nuclear Hormone Receptor DAX-1.

Degree: MSin Biology, Biology, 2014, University of San Francisco

  DAX-1 (NR0B1) is an orphan nuclear receptor that plays a key role in the development and maintenance of steroidogenic tissue in mammals. Dax-1 is… (more)

Subjects/Keywords: nuclear receptors; DAX-1; NR0B1; endocrinology; hormone receptors; cancer; Biochemistry, Biophysics, and Structural Biology; Biology; Cell and Developmental Biology; Genetics and Genomics

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APA (6th Edition):

Heskett, M. B. (2014). Epigenetic Regulation of Nuclear Hormone Receptor DAX-1. (Thesis). University of San Francisco. Retrieved from https://repository.usfca.edu/thes/116

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):

Heskett, Michael B. “Epigenetic Regulation of Nuclear Hormone Receptor DAX-1.” 2014. Thesis, University of San Francisco. Accessed November 27, 2020. https://repository.usfca.edu/thes/116.

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

MLA Handbook (7th Edition):

Heskett, Michael B. “Epigenetic Regulation of Nuclear Hormone Receptor DAX-1.” 2014. Web. 27 Nov 2020.

Vancouver:

Heskett MB. Epigenetic Regulation of Nuclear Hormone Receptor DAX-1. [Internet] [Thesis]. University of San Francisco; 2014. [cited 2020 Nov 27]. Available from: https://repository.usfca.edu/thes/116.

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

Council of Science Editors:

Heskett MB. Epigenetic Regulation of Nuclear Hormone Receptor DAX-1. [Thesis]. University of San Francisco; 2014. Available from: https://repository.usfca.edu/thes/116

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

19. Goodman, Robert. Expression and modulation of the UGT1A family of phase II metabolism genes via liganded vitamin D receptor.

Degree: PhD, 2018, Ulster University

 Phase two metabolic genes are primary targets for a range of nuclear receptors within the body. These include but are not limited to PXR, FXR,… (more)

Subjects/Keywords: Nuclear receptors; Enzymes; Metabolism

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APA (6th Edition):

Goodman, R. (2018). Expression and modulation of the UGT1A family of phase II metabolism genes via liganded vitamin D receptor. (Doctoral Dissertation). Ulster University. Retrieved from https://ulster.pure.elsevier.com/en/studentTheses/6a74090a-9f22-45fe-ba4f-b762327f1432 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.793660

Chicago Manual of Style (16th Edition):

Goodman, Robert. “Expression and modulation of the UGT1A family of phase II metabolism genes via liganded vitamin D receptor.” 2018. Doctoral Dissertation, Ulster University. Accessed November 27, 2020. https://ulster.pure.elsevier.com/en/studentTheses/6a74090a-9f22-45fe-ba4f-b762327f1432 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.793660.

MLA Handbook (7th Edition):

Goodman, Robert. “Expression and modulation of the UGT1A family of phase II metabolism genes via liganded vitamin D receptor.” 2018. Web. 27 Nov 2020.

Vancouver:

Goodman R. Expression and modulation of the UGT1A family of phase II metabolism genes via liganded vitamin D receptor. [Internet] [Doctoral dissertation]. Ulster University; 2018. [cited 2020 Nov 27]. Available from: https://ulster.pure.elsevier.com/en/studentTheses/6a74090a-9f22-45fe-ba4f-b762327f1432 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.793660.

Council of Science Editors:

Goodman R. Expression and modulation of the UGT1A family of phase II metabolism genes via liganded vitamin D receptor. [Doctoral Dissertation]. Ulster University; 2018. Available from: https://ulster.pure.elsevier.com/en/studentTheses/6a74090a-9f22-45fe-ba4f-b762327f1432 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.793660


Rutgers University

20. Ribay, Kathryn, 1984-. Hybrid modeling of estrogen receptor binding agents using advanced cheminformatics tools and massive public data.

Degree: MS, Chemistry, 2016, Rutgers University

 Estrogen receptor-α (ERα) is a critical target for drug design as well as a potential source of toxicity when activated unintentionally. Thus, evaluating potential ERα… (more)

Subjects/Keywords: QSAR (Biochemistry); Estrogen – Receptors

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APA (6th Edition):

Ribay, Kathryn, 1. (2016). Hybrid modeling of estrogen receptor binding agents using advanced cheminformatics tools and massive public data. (Masters Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/49078/

Chicago Manual of Style (16th Edition):

Ribay, Kathryn, 1984-. “Hybrid modeling of estrogen receptor binding agents using advanced cheminformatics tools and massive public data.” 2016. Masters Thesis, Rutgers University. Accessed November 27, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/49078/.

MLA Handbook (7th Edition):

Ribay, Kathryn, 1984-. “Hybrid modeling of estrogen receptor binding agents using advanced cheminformatics tools and massive public data.” 2016. Web. 27 Nov 2020.

Vancouver:

Ribay, Kathryn 1. Hybrid modeling of estrogen receptor binding agents using advanced cheminformatics tools and massive public data. [Internet] [Masters thesis]. Rutgers University; 2016. [cited 2020 Nov 27]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/49078/.

Council of Science Editors:

Ribay, Kathryn 1. Hybrid modeling of estrogen receptor binding agents using advanced cheminformatics tools and massive public data. [Masters Thesis]. Rutgers University; 2016. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/49078/

21. Xia, Gang. Structural studies of the ligand binding domain of the human retinoid X receptor bound to retinoids and the coactivator peptide GRIP-1.

Degree: PhD, 2010, University of Alabama – Birmingham

Retinoid X receptors (RXRs) are ligand–dependent transcription factors which belong to the nuclear receptor (NR) superfamily. When a ligand binds to RXRs, it activates the… (more)

Subjects/Keywords: Retinoids <; br>; Tretinoin  – Receptors  – Structure <; br>; Receptor-ligand complexes <; br>; Nuclear receptors (Biochemistry)  – Structure <; br>; Hormone receptors  – Structure <; br>; Peptides <; br>; Antineoplastic agents  – Synthesis

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APA (6th Edition):

Xia, G. (2010). Structural studies of the ligand binding domain of the human retinoid X receptor bound to retinoids and the coactivator peptide GRIP-1. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,850

Chicago Manual of Style (16th Edition):

Xia, Gang. “Structural studies of the ligand binding domain of the human retinoid X receptor bound to retinoids and the coactivator peptide GRIP-1.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed November 27, 2020. http://contentdm.mhsl.uab.edu/u?/etd,850.

MLA Handbook (7th Edition):

Xia, Gang. “Structural studies of the ligand binding domain of the human retinoid X receptor bound to retinoids and the coactivator peptide GRIP-1.” 2010. Web. 27 Nov 2020.

Vancouver:

Xia G. Structural studies of the ligand binding domain of the human retinoid X receptor bound to retinoids and the coactivator peptide GRIP-1. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2020 Nov 27]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,850.

Council of Science Editors:

Xia G. Structural studies of the ligand binding domain of the human retinoid X receptor bound to retinoids and the coactivator peptide GRIP-1. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,850


Michigan State University

22. Li, Chao. Characterization of nuclear receptors of the ecdysone gene regulatory hierachy during mosquito vitellogenesis.

Degree: PhD, Genetics Program, 2001, Michigan State University

Subjects/Keywords: Mosquitoes – Genetics; Insect hormones – Receptors; Steroid hormones – Receptors; Nuclear receptors (Biochemistry); Ecdysone; Genetic regulation

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APA (6th Edition):

Li, C. (2001). Characterization of nuclear receptors of the ecdysone gene regulatory hierachy during mosquito vitellogenesis. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:31053

Chicago Manual of Style (16th Edition):

Li, Chao. “Characterization of nuclear receptors of the ecdysone gene regulatory hierachy during mosquito vitellogenesis.” 2001. Doctoral Dissertation, Michigan State University. Accessed November 27, 2020. http://etd.lib.msu.edu/islandora/object/etd:31053.

MLA Handbook (7th Edition):

Li, Chao. “Characterization of nuclear receptors of the ecdysone gene regulatory hierachy during mosquito vitellogenesis.” 2001. Web. 27 Nov 2020.

Vancouver:

Li C. Characterization of nuclear receptors of the ecdysone gene regulatory hierachy during mosquito vitellogenesis. [Internet] [Doctoral dissertation]. Michigan State University; 2001. [cited 2020 Nov 27]. Available from: http://etd.lib.msu.edu/islandora/object/etd:31053.

Council of Science Editors:

Li C. Characterization of nuclear receptors of the ecdysone gene regulatory hierachy during mosquito vitellogenesis. [Doctoral Dissertation]. Michigan State University; 2001. Available from: http://etd.lib.msu.edu/islandora/object/etd:31053


Universitat de Barcelona

23. Lecina Casas, Daniel. Studying protein-ligand interactions using a Monte Carlo procedure.

Degree: 2017, Universitat de Barcelona

 Las simulaciones biomoleculares se han usado ampliamente en el estudio de interacciones proteína-ligando. Comprender los mecanismos involucrados en la predicción de afinidades de unión tiene… (more)

Subjects/Keywords: Biologia molecular; Biología molecular; Molecular biology; Mètode de Montecarlo; Método de Montecarlo; Monte Carlo method; Processos de Markov; Procesos de Markov; Markov processes; Lligands (Bioquímica); Ligandos (Bioquímica); Ligands (Biochemistry); Receptors nuclears (Bioquímica); Receptores nucleares (Bioquímica); Nuclear receptors (Biochemistry); Ciències Experimentals i Matemàtiques; 53

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APA (6th Edition):

Lecina Casas, D. (2017). Studying protein-ligand interactions using a Monte Carlo procedure. (Thesis). Universitat de Barcelona. Retrieved from http://hdl.handle.net/10803/459297

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):

Lecina Casas, Daniel. “Studying protein-ligand interactions using a Monte Carlo procedure.” 2017. Thesis, Universitat de Barcelona. Accessed November 27, 2020. http://hdl.handle.net/10803/459297.

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

MLA Handbook (7th Edition):

Lecina Casas, Daniel. “Studying protein-ligand interactions using a Monte Carlo procedure.” 2017. Web. 27 Nov 2020.

Vancouver:

Lecina Casas D. Studying protein-ligand interactions using a Monte Carlo procedure. [Internet] [Thesis]. Universitat de Barcelona; 2017. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10803/459297.

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

Council of Science Editors:

Lecina Casas D. Studying protein-ligand interactions using a Monte Carlo procedure. [Thesis]. Universitat de Barcelona; 2017. Available from: http://hdl.handle.net/10803/459297

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


University of Hong Kong

24. Xiao, Jing. Crosstalk between peroxisome proliferator-activated receptor-[gamma] and angiotensin II in renal proximal tubular epithelial cells in IgAnephropathy.

Degree: 2009, University of Hong Kong

Subjects/Keywords: IgA glomeruleonephritis - Genetic aspects.; Epithelial cells.; Angiotensin II.; Nuclear receptors (Biochemistry)

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APA (6th Edition):

Xiao, J. (2009). Crosstalk between peroxisome proliferator-activated receptor-[gamma] and angiotensin II in renal proximal tubular epithelial cells in IgAnephropathy. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/55529

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, Jing. “Crosstalk between peroxisome proliferator-activated receptor-[gamma] and angiotensin II in renal proximal tubular epithelial cells in IgAnephropathy.” 2009. Thesis, University of Hong Kong. Accessed November 27, 2020. http://hdl.handle.net/10722/55529.

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

MLA Handbook (7th Edition):

Xiao, Jing. “Crosstalk between peroxisome proliferator-activated receptor-[gamma] and angiotensin II in renal proximal tubular epithelial cells in IgAnephropathy.” 2009. Web. 27 Nov 2020.

Vancouver:

Xiao J. Crosstalk between peroxisome proliferator-activated receptor-[gamma] and angiotensin II in renal proximal tubular epithelial cells in IgAnephropathy. [Internet] [Thesis]. University of Hong Kong; 2009. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10722/55529.

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

Council of Science Editors:

Xiao J. Crosstalk between peroxisome proliferator-activated receptor-[gamma] and angiotensin II in renal proximal tubular epithelial cells in IgAnephropathy. [Thesis]. University of Hong Kong; 2009. Available from: http://hdl.handle.net/10722/55529

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


University of Oklahoma

25. Wu, Xiaohui. Physical characterization of the ecdysteroid and retinoid X receptor (UpEcR and UpRXR) in the fiddler crab Uca pugilator.

Degree: PhD, Department of Biology, 2003, University of Oklahoma

 EcR and RXR gene homologs in U. pugilator ( UpEcR and UpRXR) have been previously cloned. Library screenings recovered cDNA clones containing a unique amino… (more)

Subjects/Keywords: Gene expression.; Biology, Zoology.; Nuclear receptors (Biochemistry); Ecdysteroids.; Biology, Molecular.; Fiddler crabs.

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APA (6th Edition):

Wu, X. (2003). Physical characterization of the ecdysteroid and retinoid X receptor (UpEcR and UpRXR) in the fiddler crab Uca pugilator. (Doctoral Dissertation). University of Oklahoma. Retrieved from http://hdl.handle.net/11244/685

Chicago Manual of Style (16th Edition):

Wu, Xiaohui. “Physical characterization of the ecdysteroid and retinoid X receptor (UpEcR and UpRXR) in the fiddler crab Uca pugilator.” 2003. Doctoral Dissertation, University of Oklahoma. Accessed November 27, 2020. http://hdl.handle.net/11244/685.

MLA Handbook (7th Edition):

Wu, Xiaohui. “Physical characterization of the ecdysteroid and retinoid X receptor (UpEcR and UpRXR) in the fiddler crab Uca pugilator.” 2003. Web. 27 Nov 2020.

Vancouver:

Wu X. Physical characterization of the ecdysteroid and retinoid X receptor (UpEcR and UpRXR) in the fiddler crab Uca pugilator. [Internet] [Doctoral dissertation]. University of Oklahoma; 2003. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/11244/685.

Council of Science Editors:

Wu X. Physical characterization of the ecdysteroid and retinoid X receptor (UpEcR and UpRXR) in the fiddler crab Uca pugilator. [Doctoral Dissertation]. University of Oklahoma; 2003. Available from: http://hdl.handle.net/11244/685

26. Taylor, Jennifer. Engineering and improving a molecular switch system for gene therapy applications.

Degree: PhD, Chemistry and Biochemistry, 2011, Georgia Tech

 Molecular switch systems that activate gene expression by a small molecule are effective technologies that are widely used in applied biological research. Previously, two orthogonal… (more)

Subjects/Keywords: Protein engineering; Gene therapy; Molecular switch systems; Gene regulation systems; RXR; Nuclear receptors; Gene therapy; Nuclear receptors (Biochemistry); Ligands (Biochemistry)

…developed as potential molecular switch systems by modifying nuclear receptors, ligand-activated… …Receptors Nuclear receptors (NR) are a superfamily of proteins that have the ability to… …of the human genome has lead to the identification of 48 human nuclear receptors [4, 6… …x29; and tailless homolog (TLX). 1 Nuclear receptors have been implicated in… …many nuclear receptors are significant drug targets: 10-20% of drugs currently on the market… 

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

APA (6th Edition):

Taylor, J. (2011). Engineering and improving a molecular switch system for gene therapy applications. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/39501

Chicago Manual of Style (16th Edition):

Taylor, Jennifer. “Engineering and improving a molecular switch system for gene therapy applications.” 2011. Doctoral Dissertation, Georgia Tech. Accessed November 27, 2020. http://hdl.handle.net/1853/39501.

MLA Handbook (7th Edition):

Taylor, Jennifer. “Engineering and improving a molecular switch system for gene therapy applications.” 2011. Web. 27 Nov 2020.

Vancouver:

Taylor J. Engineering and improving a molecular switch system for gene therapy applications. [Internet] [Doctoral dissertation]. Georgia Tech; 2011. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1853/39501.

Council of Science Editors:

Taylor J. Engineering and improving a molecular switch system for gene therapy applications. [Doctoral Dissertation]. Georgia Tech; 2011. Available from: http://hdl.handle.net/1853/39501


University of Texas Southwestern Medical Center

27. Atkin, Stan Dean. Liver Receptor Homolog-1 Regulates Kisspeptin Expression in the Arcuate Nucleus to Promote Reproductive Axis Function.

Degree: 2014, University of Texas Southwestern Medical Center

 The timing of ovulation in mammals is set by a complex hypothalamic pituitary neuroendocrine axis. Kisspeptin neurons in the arcuate nucleus (Arc) are thought to… (more)

Subjects/Keywords: Kisspeptins; Neuropeptides; Receptors, Cytoplasmic and Nuclear; Reproduction

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

APA (6th Edition):

Atkin, S. D. (2014). Liver Receptor Homolog-1 Regulates Kisspeptin Expression in the Arcuate Nucleus to Promote Reproductive Axis Function. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1425

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):

Atkin, Stan Dean. “Liver Receptor Homolog-1 Regulates Kisspeptin Expression in the Arcuate Nucleus to Promote Reproductive Axis Function.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed November 27, 2020. http://hdl.handle.net/2152.5/1425.

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

MLA Handbook (7th Edition):

Atkin, Stan Dean. “Liver Receptor Homolog-1 Regulates Kisspeptin Expression in the Arcuate Nucleus to Promote Reproductive Axis Function.” 2014. Web. 27 Nov 2020.

Vancouver:

Atkin SD. Liver Receptor Homolog-1 Regulates Kisspeptin Expression in the Arcuate Nucleus to Promote Reproductive Axis Function. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152.5/1425.

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

Council of Science Editors:

Atkin SD. Liver Receptor Homolog-1 Regulates Kisspeptin Expression in the Arcuate Nucleus to Promote Reproductive Axis Function. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/1425

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


University of Illinois – Chicago

28. Reese, Vanessa. Transcriptional Regulation of Hepatitis B Virus Biosynthesis by Bile Acids and FoxA Factors.

Degree: 2014, University of Illinois – Chicago

 HBV is a major human pathogen that currently chronically infects approximately 400 million individuals worldwide and is responsible for about one million deaths annually. New… (more)

Subjects/Keywords: Hepatitis B Virus; HBV; FoxA; nuclear receptors

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

APA (6th Edition):

Reese, V. (2014). Transcriptional Regulation of Hepatitis B Virus Biosynthesis by Bile Acids and FoxA Factors. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/18910

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):

Reese, Vanessa. “Transcriptional Regulation of Hepatitis B Virus Biosynthesis by Bile Acids and FoxA Factors.” 2014. Thesis, University of Illinois – Chicago. Accessed November 27, 2020. http://hdl.handle.net/10027/18910.

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

MLA Handbook (7th Edition):

Reese, Vanessa. “Transcriptional Regulation of Hepatitis B Virus Biosynthesis by Bile Acids and FoxA Factors.” 2014. Web. 27 Nov 2020.

Vancouver:

Reese V. Transcriptional Regulation of Hepatitis B Virus Biosynthesis by Bile Acids and FoxA Factors. [Internet] [Thesis]. University of Illinois – Chicago; 2014. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10027/18910.

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

Council of Science Editors:

Reese V. Transcriptional Regulation of Hepatitis B Virus Biosynthesis by Bile Acids and FoxA Factors. [Thesis]. University of Illinois – Chicago; 2014. Available from: http://hdl.handle.net/10027/18910

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

29. Kaur, Satwant. Integrated strategies for investigating endocrine mechanisms in Biomphalaria glabrata as a test organism for androgenic chemical testing.

Degree: PhD, 2015, Brunel University

 Endocrine and metabolic disease or dysfunctions are of growing concern in modern societies across the globe, underlining the need for continued focus on the development… (more)

Subjects/Keywords: 572.8; Gastropod; Pulmonata; Nuclear receptors; androgens; Neuropeptide

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

APA (6th Edition):

Kaur, S. (2015). Integrated strategies for investigating endocrine mechanisms in Biomphalaria glabrata as a test organism for androgenic chemical testing. (Doctoral Dissertation). Brunel University. Retrieved from http://bura.brunel.ac.uk/handle/2438/10544 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.646260

Chicago Manual of Style (16th Edition):

Kaur, Satwant. “Integrated strategies for investigating endocrine mechanisms in Biomphalaria glabrata as a test organism for androgenic chemical testing.” 2015. Doctoral Dissertation, Brunel University. Accessed November 27, 2020. http://bura.brunel.ac.uk/handle/2438/10544 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.646260.

MLA Handbook (7th Edition):

Kaur, Satwant. “Integrated strategies for investigating endocrine mechanisms in Biomphalaria glabrata as a test organism for androgenic chemical testing.” 2015. Web. 27 Nov 2020.

Vancouver:

Kaur S. Integrated strategies for investigating endocrine mechanisms in Biomphalaria glabrata as a test organism for androgenic chemical testing. [Internet] [Doctoral dissertation]. Brunel University; 2015. [cited 2020 Nov 27]. Available from: http://bura.brunel.ac.uk/handle/2438/10544 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.646260.

Council of Science Editors:

Kaur S. Integrated strategies for investigating endocrine mechanisms in Biomphalaria glabrata as a test organism for androgenic chemical testing. [Doctoral Dissertation]. Brunel University; 2015. Available from: http://bura.brunel.ac.uk/handle/2438/10544 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.646260


University of Glasgow

30. Logie, Colin. Ligand regulated site specific recombination in mammalian cells.

Degree: PhD, 1995, University of Glasgow

 Chapter 1 of this thesis summarizes the current knowledge about the nuclear receptor superfamily of transcription factors. Chapter 2 describes the materials and methods used… (more)

Subjects/Keywords: 572.8; Nuclear receptors

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

APA (6th Edition):

Logie, C. (1995). Ligand regulated site specific recombination in mammalian cells. (Doctoral Dissertation). University of Glasgow. Retrieved from http://theses.gla.ac.uk/75539/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.284710

Chicago Manual of Style (16th Edition):

Logie, Colin. “Ligand regulated site specific recombination in mammalian cells.” 1995. Doctoral Dissertation, University of Glasgow. Accessed November 27, 2020. http://theses.gla.ac.uk/75539/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.284710.

MLA Handbook (7th Edition):

Logie, Colin. “Ligand regulated site specific recombination in mammalian cells.” 1995. Web. 27 Nov 2020.

Vancouver:

Logie C. Ligand regulated site specific recombination in mammalian cells. [Internet] [Doctoral dissertation]. University of Glasgow; 1995. [cited 2020 Nov 27]. Available from: http://theses.gla.ac.uk/75539/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.284710.

Council of Science Editors:

Logie C. Ligand regulated site specific recombination in mammalian cells. [Doctoral Dissertation]. University of Glasgow; 1995. Available from: http://theses.gla.ac.uk/75539/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.284710

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