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You searched for subject:(Nuclear receptors). Showing records 1 – 30 of 221 total matches.

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1. 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 October 22, 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. 22 Oct 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 Oct 22]. 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

2. 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 (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 October 22, 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. 22 Oct 2020.

Vancouver:

Noto PB. Analysis of Liver X Receptor target gene expression across species. [Internet] [Thesis]. Drexel University; 2013. [cited 2020 Oct 22]. 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


University of Texas Southwestern Medical Center

3. 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 (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 October 22, 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. 22 Oct 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 Oct 22]. 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


Oregon State University

4. 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 October 22, 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. 22 Oct 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 Oct 22]. 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


University of Illinois – Chicago

5. 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 (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 October 22, 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. 22 Oct 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 Oct 22]. 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

6. 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 (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 October 22, 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. 22 Oct 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 Oct 22]. 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

7. 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 (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 October 22, 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. 22 Oct 2020.

Vancouver:

Logie C. Ligand regulated site specific recombination in mammalian cells. [Internet] [Doctoral dissertation]. University of Glasgow; 1995. [cited 2020 Oct 22]. 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


University of Cambridge

8. Di Canio, Ludovica. Regulation of oligodendrocyte lineage cell function by the RXRγ nuclear receptor.

Degree: PhD, 2019, University of Cambridge

 Remyelination is a spontaneous regenerative process whereby myelin sheaths are restored to demyelinated axons. Key players in this process are oligodendrocyte progenitor cells (OPCs), a… (more)

Subjects/Keywords: oligodendrocyte; nuclear receptors; remyelination; rxr; opc

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APA (6th Edition):

Di Canio, L. (2019). Regulation of oligodendrocyte lineage cell function by the RXRγ nuclear receptor. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.36392 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767819

Chicago Manual of Style (16th Edition):

Di Canio, Ludovica. “Regulation of oligodendrocyte lineage cell function by the RXRγ nuclear receptor.” 2019. Doctoral Dissertation, University of Cambridge. Accessed October 22, 2020. https://doi.org/10.17863/CAM.36392 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767819.

MLA Handbook (7th Edition):

Di Canio, Ludovica. “Regulation of oligodendrocyte lineage cell function by the RXRγ nuclear receptor.” 2019. Web. 22 Oct 2020.

Vancouver:

Di Canio L. Regulation of oligodendrocyte lineage cell function by the RXRγ nuclear receptor. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Oct 22]. Available from: https://doi.org/10.17863/CAM.36392 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767819.

Council of Science Editors:

Di Canio L. Regulation of oligodendrocyte lineage cell function by the RXRγ nuclear receptor. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://doi.org/10.17863/CAM.36392 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767819


East Carolina University

9. Wang, Lei. Retinoids Potentiate Clinically Relevant Cellular Responses through RARα/RXR Nuclear Receptor Synergism in Cutaneous T Cell Lymphoma.

Degree: PhD, PHD-Biochem and Molecular Biology, 2015, East Carolina University

 The heterogeneity of cutaneous T cell lymphoma (CTCL) has stifled treatment options and hindered cure development. Despite the heterogeneous nature of CTCLs, a hallmark of… (more)

Subjects/Keywords: Vitamin A; Adhesion; Lymphoma, T-Cell, Cutaneous; Retinoids; Receptors, Cytoplasmic and Nuclear; Receptors, Retinoic Acid

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APA (6th Edition):

Wang, L. (2015). Retinoids Potentiate Clinically Relevant Cellular Responses through RARα/RXR Nuclear Receptor Synergism in Cutaneous T Cell Lymphoma. (Doctoral Dissertation). East Carolina University. Retrieved from http://hdl.handle.net/10342/5124

Chicago Manual of Style (16th Edition):

Wang, Lei. “Retinoids Potentiate Clinically Relevant Cellular Responses through RARα/RXR Nuclear Receptor Synergism in Cutaneous T Cell Lymphoma.” 2015. Doctoral Dissertation, East Carolina University. Accessed October 22, 2020. http://hdl.handle.net/10342/5124.

MLA Handbook (7th Edition):

Wang, Lei. “Retinoids Potentiate Clinically Relevant Cellular Responses through RARα/RXR Nuclear Receptor Synergism in Cutaneous T Cell Lymphoma.” 2015. Web. 22 Oct 2020.

Vancouver:

Wang L. Retinoids Potentiate Clinically Relevant Cellular Responses through RARα/RXR Nuclear Receptor Synergism in Cutaneous T Cell Lymphoma. [Internet] [Doctoral dissertation]. East Carolina University; 2015. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/10342/5124.

Council of Science Editors:

Wang L. Retinoids Potentiate Clinically Relevant Cellular Responses through RARα/RXR Nuclear Receptor Synergism in Cutaneous T Cell Lymphoma. [Doctoral Dissertation]. East Carolina University; 2015. Available from: http://hdl.handle.net/10342/5124


University of Houston

10. Folly-Kossi, Helena 1984-. Nuclear Receptors in Breast Cancer.

Degree: PhD, Cell and Molecular Biology, 2017, University of Houston

 Breast cancer (BC) is classified into four major molecular subtypes. The most predominant subtypes, luminal A and B are hormone receptor-positive BC (ERα +/PR+) which… (more)

Subjects/Keywords: Nuclear receptors; Breast cancer; Survival analysis; Endocrine therapy; Tamoxifen resistance; Glucocorticoid receptors; Estrogen receptors; Clinical data

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APA (6th Edition):

Folly-Kossi, H. 1. (2017). Nuclear Receptors in Breast Cancer. (Doctoral Dissertation). University of Houston. Retrieved from http://hdl.handle.net/10657/4586

Chicago Manual of Style (16th Edition):

Folly-Kossi, Helena 1984-. “Nuclear Receptors in Breast Cancer.” 2017. Doctoral Dissertation, University of Houston. Accessed October 22, 2020. http://hdl.handle.net/10657/4586.

MLA Handbook (7th Edition):

Folly-Kossi, Helena 1984-. “Nuclear Receptors in Breast Cancer.” 2017. Web. 22 Oct 2020.

Vancouver:

Folly-Kossi H1. Nuclear Receptors in Breast Cancer. [Internet] [Doctoral dissertation]. University of Houston; 2017. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/10657/4586.

Council of Science Editors:

Folly-Kossi H1. Nuclear Receptors in Breast Cancer. [Doctoral Dissertation]. University of Houston; 2017. Available from: http://hdl.handle.net/10657/4586


University of Texas Southwestern Medical Center

11. Fung, Ho Yee Joyce. Nuclear Export Receptor CRM1 Recognizes Nuclear Export Signals with Diverse Conformations.

Degree: 2017, University of Texas Southwestern Medical Center

 The Chromosome Region of Maintenance 1 or CRM1 protein facilitates export of hundreds of proteins and RNA molecules from eukaryotic cell nuclei. CRM1 recognizes its… (more)

Subjects/Keywords: Active Transport, Cell Nucleus; Cell Nucleus; Karyopherins; Nuclear Export Signals; Receptors, Cytoplasmic and Nuclear

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APA (6th Edition):

Fung, H. Y. J. (2017). Nuclear Export Receptor CRM1 Recognizes Nuclear Export Signals with Diverse Conformations. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/6615

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):

Fung, Ho Yee Joyce. “Nuclear Export Receptor CRM1 Recognizes Nuclear Export Signals with Diverse Conformations.” 2017. Thesis, University of Texas Southwestern Medical Center. Accessed October 22, 2020. http://hdl.handle.net/2152.5/6615.

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

MLA Handbook (7th Edition):

Fung, Ho Yee Joyce. “Nuclear Export Receptor CRM1 Recognizes Nuclear Export Signals with Diverse Conformations.” 2017. Web. 22 Oct 2020.

Vancouver:

Fung HYJ. Nuclear Export Receptor CRM1 Recognizes Nuclear Export Signals with Diverse Conformations. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2017. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/2152.5/6615.

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

Council of Science Editors:

Fung HYJ. Nuclear Export Receptor CRM1 Recognizes Nuclear Export Signals with Diverse Conformations. [Thesis]. University of Texas Southwestern Medical Center; 2017. Available from: http://hdl.handle.net/2152.5/6615

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


Universiteit Utrecht

12. Timmermans, L.P.M. Nuclear Receptors in Immunity: Molecular Mechanisms of GR, PPARγ and LXR in Inflammatory Gene Regulation.

Degree: 2010, Universiteit Utrecht

Nuclear receptors are known to be involved in many processes in the metabolism, reproduction, cell growth and immunity. Several nuclear receptors are indispensable factors in… (more)

Subjects/Keywords: Geneeskunde; Nuclear receptors, PPARγ, GR, LXR, Inflammatory gene regulation

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APA (6th Edition):

Timmermans, L. P. M. (2010). Nuclear Receptors in Immunity: Molecular Mechanisms of GR, PPARγ and LXR in Inflammatory Gene Regulation. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/44728

Chicago Manual of Style (16th Edition):

Timmermans, L P M. “Nuclear Receptors in Immunity: Molecular Mechanisms of GR, PPARγ and LXR in Inflammatory Gene Regulation.” 2010. Masters Thesis, Universiteit Utrecht. Accessed October 22, 2020. http://dspace.library.uu.nl:8080/handle/1874/44728.

MLA Handbook (7th Edition):

Timmermans, L P M. “Nuclear Receptors in Immunity: Molecular Mechanisms of GR, PPARγ and LXR in Inflammatory Gene Regulation.” 2010. Web. 22 Oct 2020.

Vancouver:

Timmermans LPM. Nuclear Receptors in Immunity: Molecular Mechanisms of GR, PPARγ and LXR in Inflammatory Gene Regulation. [Internet] [Masters thesis]. Universiteit Utrecht; 2010. [cited 2020 Oct 22]. Available from: http://dspace.library.uu.nl:8080/handle/1874/44728.

Council of Science Editors:

Timmermans LPM. Nuclear Receptors in Immunity: Molecular Mechanisms of GR, PPARγ and LXR in Inflammatory Gene Regulation. [Masters Thesis]. Universiteit Utrecht; 2010. Available from: http://dspace.library.uu.nl:8080/handle/1874/44728


Universiteit Utrecht

13. Geffen, J.P. van. Glucocorticoid Receptor Function and Hormone Therapy Resistance.

Degree: 2013, Universiteit Utrecht

Nuclear receptors (NRs) are a superfamily of transcription factors that can be activated by ligands and thereby regulate the activation of a variety of genes… (more)

Subjects/Keywords: asthma; resistance; nuclear receptors; glucocorticoids; coactivators; corepressors; posttranscriptional modifications

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APA (6th Edition):

Geffen, J. P. v. (2013). Glucocorticoid Receptor Function and Hormone Therapy Resistance. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/277876

Chicago Manual of Style (16th Edition):

Geffen, J P van. “Glucocorticoid Receptor Function and Hormone Therapy Resistance.” 2013. Masters Thesis, Universiteit Utrecht. Accessed October 22, 2020. http://dspace.library.uu.nl:8080/handle/1874/277876.

MLA Handbook (7th Edition):

Geffen, J P van. “Glucocorticoid Receptor Function and Hormone Therapy Resistance.” 2013. Web. 22 Oct 2020.

Vancouver:

Geffen JPv. Glucocorticoid Receptor Function and Hormone Therapy Resistance. [Internet] [Masters thesis]. Universiteit Utrecht; 2013. [cited 2020 Oct 22]. Available from: http://dspace.library.uu.nl:8080/handle/1874/277876.

Council of Science Editors:

Geffen JPv. Glucocorticoid Receptor Function and Hormone Therapy Resistance. [Masters Thesis]. Universiteit Utrecht; 2013. Available from: http://dspace.library.uu.nl:8080/handle/1874/277876


Universiteit Utrecht

14. Hollman, D.A.A. Transactivation versus transrepression in FXR: lessons learned from other Nuclear Receptors.

Degree: 2011, Universiteit Utrecht

 Farnesoid X Receptor (FXR) is an important player in the upregulation of genes (transactivation) in bile acid homeostasis and fat and glucose metabolism. Recently, it… (more)

Subjects/Keywords: Nuclear Receptors; Farnesoid X Receptor; Transactivation; Transrepression; Post-translational modifications

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APA (6th Edition):

Hollman, D. A. A. (2011). Transactivation versus transrepression in FXR: lessons learned from other Nuclear Receptors. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/208274

Chicago Manual of Style (16th Edition):

Hollman, D A A. “Transactivation versus transrepression in FXR: lessons learned from other Nuclear Receptors.” 2011. Masters Thesis, Universiteit Utrecht. Accessed October 22, 2020. http://dspace.library.uu.nl:8080/handle/1874/208274.

MLA Handbook (7th Edition):

Hollman, D A A. “Transactivation versus transrepression in FXR: lessons learned from other Nuclear Receptors.” 2011. Web. 22 Oct 2020.

Vancouver:

Hollman DAA. Transactivation versus transrepression in FXR: lessons learned from other Nuclear Receptors. [Internet] [Masters thesis]. Universiteit Utrecht; 2011. [cited 2020 Oct 22]. Available from: http://dspace.library.uu.nl:8080/handle/1874/208274.

Council of Science Editors:

Hollman DAA. Transactivation versus transrepression in FXR: lessons learned from other Nuclear Receptors. [Masters Thesis]. Universiteit Utrecht; 2011. Available from: http://dspace.library.uu.nl:8080/handle/1874/208274

15. van Gogh, IJA. Nuclear receptors and myokines : mediators of exercise-induced skeletal muscle metabolism.

Degree: 2016, Universiteit Utrecht

 Skeletal muscle is a crucial organ in mediating (exercise-induced) beneficial health effects. In this thesis we gained important knowledge on the molecular biology of the… (more)

Subjects/Keywords: Exercise; myokines; nuclear receptors; metabolism; skeletal muscle; Nur77; LXRβ; MCP-1

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APA (6th Edition):

van Gogh, I. (2016). Nuclear receptors and myokines : mediators of exercise-induced skeletal muscle metabolism. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/333972

Chicago Manual of Style (16th Edition):

van Gogh, IJA. “Nuclear receptors and myokines : mediators of exercise-induced skeletal muscle metabolism.” 2016. Doctoral Dissertation, Universiteit Utrecht. Accessed October 22, 2020. http://dspace.library.uu.nl:8080/handle/1874/333972.

MLA Handbook (7th Edition):

van Gogh, IJA. “Nuclear receptors and myokines : mediators of exercise-induced skeletal muscle metabolism.” 2016. Web. 22 Oct 2020.

Vancouver:

van Gogh I. Nuclear receptors and myokines : mediators of exercise-induced skeletal muscle metabolism. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2016. [cited 2020 Oct 22]. Available from: http://dspace.library.uu.nl:8080/handle/1874/333972.

Council of Science Editors:

van Gogh I. Nuclear receptors and myokines : mediators of exercise-induced skeletal muscle metabolism. [Doctoral Dissertation]. Universiteit Utrecht; 2016. Available from: http://dspace.library.uu.nl:8080/handle/1874/333972


Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

16. Barlaka, Eleftheria. Διερεύνηση της προστατευτικής δράσης των πυρηνικών υποδοχέων PPARα και PPARβ/δ σε συνθήκες καταπόνησης των καρδιομυοκυττάρων.

Degree: 2016, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

 Heart failure still remains one of the leading causes of morbidity and mortality worldwide. A major contributing factor is reactive oxygen species (ROS) overproduction which… (more)

Subjects/Keywords: Καρδιομυοκύτταρα; Οξειδωτικό στρες; Πυρηνικοί υποδοχείς; Cardiomyocytes; Oxidative stress; Nuclear receptors

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APA (6th Edition):

Barlaka, E. (2016). Διερεύνηση της προστατευτικής δράσης των πυρηνικών υποδοχέων PPARα και PPARβ/δ σε συνθήκες καταπόνησης των καρδιομυοκυττάρων. (Thesis). Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Retrieved from http://hdl.handle.net/10442/hedi/38499

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):

Barlaka, Eleftheria. “Διερεύνηση της προστατευτικής δράσης των πυρηνικών υποδοχέων PPARα και PPARβ/δ σε συνθήκες καταπόνησης των καρδιομυοκυττάρων.” 2016. Thesis, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Accessed October 22, 2020. http://hdl.handle.net/10442/hedi/38499.

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

MLA Handbook (7th Edition):

Barlaka, Eleftheria. “Διερεύνηση της προστατευτικής δράσης των πυρηνικών υποδοχέων PPARα και PPARβ/δ σε συνθήκες καταπόνησης των καρδιομυοκυττάρων.” 2016. Web. 22 Oct 2020.

Vancouver:

Barlaka E. Διερεύνηση της προστατευτικής δράσης των πυρηνικών υποδοχέων PPARα και PPARβ/δ σε συνθήκες καταπόνησης των καρδιομυοκυττάρων. [Internet] [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2016. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/10442/hedi/38499.

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

Council of Science Editors:

Barlaka E. Διερεύνηση της προστατευτικής δράσης των πυρηνικών υποδοχέων PPARα και PPARβ/δ σε συνθήκες καταπόνησης των καρδιομυοκυττάρων. [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2016. Available from: http://hdl.handle.net/10442/hedi/38499

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


University of Saskatchewan

17. Kendall, Stephanie. Structural characterization of the N-terminal region of the Saccharomyces cerevisiae G-protein coupled receptor, Ste2p.

Degree: 2011, University of Saskatchewan

 G-protein coupled receptors (GPCRs) form a superfamily of cell surface receptors with in excess of 2000 genes identified across taxa (Pierce et al., 2002). They… (more)

Subjects/Keywords: G-protein coupled receptors; Ste2p; Nuclear magnetic resonance; Circular Dichroism

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APA (6th Edition):

Kendall, S. (2011). Structural characterization of the N-terminal region of the Saccharomyces cerevisiae G-protein coupled receptor, Ste2p. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2011-07-114

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):

Kendall, Stephanie. “Structural characterization of the N-terminal region of the Saccharomyces cerevisiae G-protein coupled receptor, Ste2p.” 2011. Thesis, University of Saskatchewan. Accessed October 22, 2020. http://hdl.handle.net/10388/ETD-2011-07-114.

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

MLA Handbook (7th Edition):

Kendall, Stephanie. “Structural characterization of the N-terminal region of the Saccharomyces cerevisiae G-protein coupled receptor, Ste2p.” 2011. Web. 22 Oct 2020.

Vancouver:

Kendall S. Structural characterization of the N-terminal region of the Saccharomyces cerevisiae G-protein coupled receptor, Ste2p. [Internet] [Thesis]. University of Saskatchewan; 2011. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/10388/ETD-2011-07-114.

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

Council of Science Editors:

Kendall S. Structural characterization of the N-terminal region of the Saccharomyces cerevisiae G-protein coupled receptor, Ste2p. [Thesis]. University of Saskatchewan; 2011. Available from: http://hdl.handle.net/10388/ETD-2011-07-114

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


University of Texas Southwestern Medical Center

18. Carrasco, Yazmin Paulina. Natural Products as Selective Chemotherapeutic Agents and as Chemical Probes to Understand Biological Processes.

Degree: 2013, University of Texas Southwestern Medical Center

 Aware of the important role that terrestrial microbial natural products play in the discovery of therapeutics and the decrease in rate of discovery of new… (more)

Subjects/Keywords: Gene Expression Regulation, Neoplastic; Fatty Acids, Unsaturated; Receptors, Cytoplasmic and Nuclear

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APA (6th Edition):

Carrasco, Y. P. (2013). Natural Products as Selective Chemotherapeutic Agents and as Chemical Probes to Understand Biological Processes. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/2716

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):

Carrasco, Yazmin Paulina. “Natural Products as Selective Chemotherapeutic Agents and as Chemical Probes to Understand Biological Processes.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed October 22, 2020. http://hdl.handle.net/2152.5/2716.

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

MLA Handbook (7th Edition):

Carrasco, Yazmin Paulina. “Natural Products as Selective Chemotherapeutic Agents and as Chemical Probes to Understand Biological Processes.” 2013. Web. 22 Oct 2020.

Vancouver:

Carrasco YP. Natural Products as Selective Chemotherapeutic Agents and as Chemical Probes to Understand Biological Processes. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/2152.5/2716.

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

Council of Science Editors:

Carrasco YP. Natural Products as Selective Chemotherapeutic Agents and as Chemical Probes to Understand Biological Processes. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/2716

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


University of Wisconsin – Milwaukee

19. Teske, Kelly Ann. Part I. The Development of Non-secosteroidal Vitamin D Receptor Modulators Part II. The Development of a Universal GTP-ase Assay.

Degree: PhD, Chemistry, 2015, University of Wisconsin – Milwaukee

  The vitamin D receptor is a nuclear hormone receptor that regulates cell proliferation, cell differentiation, calcium homeostasis and immunomodulation. The receptor is activated by… (more)

Subjects/Keywords: Assays; Gtpase; Non-Secosteroidal; Nuclear Receptors; Synthesis; Vitamin D Receptor; Chemistry

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APA (6th Edition):

Teske, K. A. (2015). Part I. The Development of Non-secosteroidal Vitamin D Receptor Modulators Part II. The Development of a Universal GTP-ase Assay. (Doctoral Dissertation). University of Wisconsin – Milwaukee. Retrieved from https://dc.uwm.edu/etd/1087

Chicago Manual of Style (16th Edition):

Teske, Kelly Ann. “Part I. The Development of Non-secosteroidal Vitamin D Receptor Modulators Part II. The Development of a Universal GTP-ase Assay.” 2015. Doctoral Dissertation, University of Wisconsin – Milwaukee. Accessed October 22, 2020. https://dc.uwm.edu/etd/1087.

MLA Handbook (7th Edition):

Teske, Kelly Ann. “Part I. The Development of Non-secosteroidal Vitamin D Receptor Modulators Part II. The Development of a Universal GTP-ase Assay.” 2015. Web. 22 Oct 2020.

Vancouver:

Teske KA. Part I. The Development of Non-secosteroidal Vitamin D Receptor Modulators Part II. The Development of a Universal GTP-ase Assay. [Internet] [Doctoral dissertation]. University of Wisconsin – Milwaukee; 2015. [cited 2020 Oct 22]. Available from: https://dc.uwm.edu/etd/1087.

Council of Science Editors:

Teske KA. Part I. The Development of Non-secosteroidal Vitamin D Receptor Modulators Part II. The Development of a Universal GTP-ase Assay. [Doctoral Dissertation]. University of Wisconsin – Milwaukee; 2015. Available from: https://dc.uwm.edu/etd/1087


University of Texas Southwestern Medical Center

20. Jones, Ryan Dale. Nuclear Hormone Receptor-Mediated Changes of Cholesterol, Triglyceride, and Bile Acid Physiology in Response to Alterations in Cholesterol Absorption and Bile Acid Pool Size in Mice.

Degree: 2013, University of Texas Southwestern Medical Center

 The regulation of lipid metabolism is an interwoven series of pathways and events acting in concert to control the nutritional and metabolic needs of the… (more)

Subjects/Keywords: Bile Acids and Salts; Cholesterol; Receptors, Cytoplasmic and Nuclear

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APA (6th Edition):

Jones, R. D. (2013). Nuclear Hormone Receptor-Mediated Changes of Cholesterol, Triglyceride, and Bile Acid Physiology in Response to Alterations in Cholesterol Absorption and Bile Acid Pool Size in Mice. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4103

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):

Jones, Ryan Dale. “Nuclear Hormone Receptor-Mediated Changes of Cholesterol, Triglyceride, and Bile Acid Physiology in Response to Alterations in Cholesterol Absorption and Bile Acid Pool Size in Mice.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed October 22, 2020. http://hdl.handle.net/2152.5/4103.

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

MLA Handbook (7th Edition):

Jones, Ryan Dale. “Nuclear Hormone Receptor-Mediated Changes of Cholesterol, Triglyceride, and Bile Acid Physiology in Response to Alterations in Cholesterol Absorption and Bile Acid Pool Size in Mice.” 2013. Web. 22 Oct 2020.

Vancouver:

Jones RD. Nuclear Hormone Receptor-Mediated Changes of Cholesterol, Triglyceride, and Bile Acid Physiology in Response to Alterations in Cholesterol Absorption and Bile Acid Pool Size in Mice. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/2152.5/4103.

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

Council of Science Editors:

Jones RD. Nuclear Hormone Receptor-Mediated Changes of Cholesterol, Triglyceride, and Bile Acid Physiology in Response to Alterations in Cholesterol Absorption and Bile Acid Pool Size in Mice. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/4103

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


University of Texas Southwestern Medical Center

21. Wang, Zhu. Nuclear Receptor Controls Nematode Metabolism And Development: Insight Into Man’s Nemesis, the Conqueror Worm.

Degree: 2011, University of Texas Southwestern Medical Center

 The nuclear receptor DAF-12 plays a central role in controlling the larval development of C. elegans. Activation of DAF-12 by its ligands called dafachronic acids… (more)

Subjects/Keywords: Receptors, Cytoplasmic and Nuclear; Growth and Development; Caenorhabditis elegans Proteins

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APA (6th Edition):

Wang, Z. (2011). Nuclear Receptor Controls Nematode Metabolism And Development: Insight Into Man’s Nemesis, the Conqueror Worm. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/855

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, Zhu. “Nuclear Receptor Controls Nematode Metabolism And Development: Insight Into Man’s Nemesis, the Conqueror Worm.” 2011. Thesis, University of Texas Southwestern Medical Center. Accessed October 22, 2020. http://hdl.handle.net/2152.5/855.

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

MLA Handbook (7th Edition):

Wang, Zhu. “Nuclear Receptor Controls Nematode Metabolism And Development: Insight Into Man’s Nemesis, the Conqueror Worm.” 2011. Web. 22 Oct 2020.

Vancouver:

Wang Z. Nuclear Receptor Controls Nematode Metabolism And Development: Insight Into Man’s Nemesis, the Conqueror Worm. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2011. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/2152.5/855.

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

Council of Science Editors:

Wang Z. Nuclear Receptor Controls Nematode Metabolism And Development: Insight Into Man’s Nemesis, the Conqueror Worm. [Thesis]. University of Texas Southwestern Medical Center; 2011. Available from: http://hdl.handle.net/2152.5/855

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

22. Markov, Gabriel. Evolution de la signalisation stéroïdienne chez les Métazoaires : Evolution of Steroid Signaling in Metazoans.

Degree: Docteur es, Sciences de la vie, 2011, Lyon, École normale supérieure

La signalisation stéroïdienne médiée par des récepteurs nucléaires est impliquée dans de nombreux processus ayant trait au développement des animaux. La compréhension de ces phénomènes… (more)

Subjects/Keywords: CYP450; Evolution; Steroids; Metazoans; Nuclear receptors; Hormones; CYP450

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APA (6th Edition):

Markov, G. (2011). Evolution de la signalisation stéroïdienne chez les Métazoaires : Evolution of Steroid Signaling in Metazoans. (Doctoral Dissertation). Lyon, École normale supérieure. Retrieved from http://www.theses.fr/2011ENSL0634

Chicago Manual of Style (16th Edition):

Markov, Gabriel. “Evolution de la signalisation stéroïdienne chez les Métazoaires : Evolution of Steroid Signaling in Metazoans.” 2011. Doctoral Dissertation, Lyon, École normale supérieure. Accessed October 22, 2020. http://www.theses.fr/2011ENSL0634.

MLA Handbook (7th Edition):

Markov, Gabriel. “Evolution de la signalisation stéroïdienne chez les Métazoaires : Evolution of Steroid Signaling in Metazoans.” 2011. Web. 22 Oct 2020.

Vancouver:

Markov G. Evolution de la signalisation stéroïdienne chez les Métazoaires : Evolution of Steroid Signaling in Metazoans. [Internet] [Doctoral dissertation]. Lyon, École normale supérieure; 2011. [cited 2020 Oct 22]. Available from: http://www.theses.fr/2011ENSL0634.

Council of Science Editors:

Markov G. Evolution de la signalisation stéroïdienne chez les Métazoaires : Evolution of Steroid Signaling in Metazoans. [Doctoral Dissertation]. Lyon, École normale supérieure; 2011. Available from: http://www.theses.fr/2011ENSL0634


University of Illinois – Chicago

23. Kramer, Kaitrin. Tumor Suppressor Regulation of the Cancer Stem Cell Niche.

Degree: 2015, University of Illinois – Chicago

 Mammary stem cells (MSC) expansion is associated with aggressive human breast cancer. Tumorigenic MSC expansion is correlated with increased angiogenesis and poor clinical prognosis in… (more)

Subjects/Keywords: Breast cancer; Nuclear receptors; Stem Cells; MicroRNA; Angiogensis; Chemotherapy

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APA (6th Edition):

Kramer, K. (2015). Tumor Suppressor Regulation of the Cancer Stem Cell Niche. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/19376

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):

Kramer, Kaitrin. “Tumor Suppressor Regulation of the Cancer Stem Cell Niche.” 2015. Thesis, University of Illinois – Chicago. Accessed October 22, 2020. http://hdl.handle.net/10027/19376.

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

MLA Handbook (7th Edition):

Kramer, Kaitrin. “Tumor Suppressor Regulation of the Cancer Stem Cell Niche.” 2015. Web. 22 Oct 2020.

Vancouver:

Kramer K. Tumor Suppressor Regulation of the Cancer Stem Cell Niche. [Internet] [Thesis]. University of Illinois – Chicago; 2015. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/10027/19376.

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

Council of Science Editors:

Kramer K. Tumor Suppressor Regulation of the Cancer Stem Cell Niche. [Thesis]. University of Illinois – Chicago; 2015. Available from: http://hdl.handle.net/10027/19376

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


Wayne State University

24. Dubaisi, Sarah Talal. Characterization Of Cytosolic Sulfotransferase Expression And Regulation In Human Liver And Intestine.

Degree: PhD, Pharmacology, 2019, Wayne State University

  SULTs are conjugation enzymes that can modify the activity of a myriad of foreign and endogenous molecules. SULT expression was detected in various human… (more)

Subjects/Keywords: Intestine; Liver; Nuclear receptors; SULT; Xenobiotic-metabolizing enzymes; Molecular Biology; Pharmacology

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APA (6th Edition):

Dubaisi, S. T. (2019). Characterization Of Cytosolic Sulfotransferase Expression And Regulation In Human Liver And Intestine. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/2158

Chicago Manual of Style (16th Edition):

Dubaisi, Sarah Talal. “Characterization Of Cytosolic Sulfotransferase Expression And Regulation In Human Liver And Intestine.” 2019. Doctoral Dissertation, Wayne State University. Accessed October 22, 2020. https://digitalcommons.wayne.edu/oa_dissertations/2158.

MLA Handbook (7th Edition):

Dubaisi, Sarah Talal. “Characterization Of Cytosolic Sulfotransferase Expression And Regulation In Human Liver And Intestine.” 2019. Web. 22 Oct 2020.

Vancouver:

Dubaisi ST. Characterization Of Cytosolic Sulfotransferase Expression And Regulation In Human Liver And Intestine. [Internet] [Doctoral dissertation]. Wayne State University; 2019. [cited 2020 Oct 22]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/2158.

Council of Science Editors:

Dubaisi ST. Characterization Of Cytosolic Sulfotransferase Expression And Regulation In Human Liver And Intestine. [Doctoral Dissertation]. Wayne State University; 2019. Available from: https://digitalcommons.wayne.edu/oa_dissertations/2158


Boston University

25. Watt, James. Identifying and modeling the contribution of nuclear receptors to environmental obesogen-induced toxicity in bone.

Degree: PhD, Environmental Health, 2016, Boston University

 Bone is a dynamic tissue, where bone forming osteoblasts and bone resorbing osteoclasts maintain homeostasis. Research into bone toxicology has largely focused on pharmaceutical side… (more)

Subjects/Keywords: Environmental health; Bone; Toxicant; Chemical mixtures; Nuclear receptors

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APA (6th Edition):

Watt, J. (2016). Identifying and modeling the contribution of nuclear receptors to environmental obesogen-induced toxicity in bone. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/19516

Chicago Manual of Style (16th Edition):

Watt, James. “Identifying and modeling the contribution of nuclear receptors to environmental obesogen-induced toxicity in bone.” 2016. Doctoral Dissertation, Boston University. Accessed October 22, 2020. http://hdl.handle.net/2144/19516.

MLA Handbook (7th Edition):

Watt, James. “Identifying and modeling the contribution of nuclear receptors to environmental obesogen-induced toxicity in bone.” 2016. Web. 22 Oct 2020.

Vancouver:

Watt J. Identifying and modeling the contribution of nuclear receptors to environmental obesogen-induced toxicity in bone. [Internet] [Doctoral dissertation]. Boston University; 2016. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/2144/19516.

Council of Science Editors:

Watt J. Identifying and modeling the contribution of nuclear receptors to environmental obesogen-induced toxicity in bone. [Doctoral Dissertation]. Boston University; 2016. Available from: http://hdl.handle.net/2144/19516


Columbia University

26. 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 October 22, 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. 22 Oct 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 Oct 22]. 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


University of Illinois – Chicago

27. Hoeppner, Crystal Z. Identification of a Nuclear Localization Sequence in Beta-Arrestin1:Implications in NF- kB Activation.

Degree: 2012, University of Illinois – Chicago

 A mounting body of evidence suggests that beta-arrestin1 plays important roles in the nucleus, but how beta-arrestin1 enters the nucleus remains unclear since no nuclear(more)

Subjects/Keywords: G Protein-Coupled Receptors; Transcription; Beta-Arrestin; Nuclear Localization

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APA (6th Edition):

Hoeppner, C. Z. (2012). Identification of a Nuclear Localization Sequence in Beta-Arrestin1:Implications in NF- kB Activation. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/9243

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):

Hoeppner, Crystal Z. “Identification of a Nuclear Localization Sequence in Beta-Arrestin1:Implications in NF- kB Activation.” 2012. Thesis, University of Illinois – Chicago. Accessed October 22, 2020. http://hdl.handle.net/10027/9243.

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

MLA Handbook (7th Edition):

Hoeppner, Crystal Z. “Identification of a Nuclear Localization Sequence in Beta-Arrestin1:Implications in NF- kB Activation.” 2012. Web. 22 Oct 2020.

Vancouver:

Hoeppner CZ. Identification of a Nuclear Localization Sequence in Beta-Arrestin1:Implications in NF- kB Activation. [Internet] [Thesis]. University of Illinois – Chicago; 2012. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/10027/9243.

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

Council of Science Editors:

Hoeppner CZ. Identification of a Nuclear Localization Sequence in Beta-Arrestin1:Implications in NF- kB Activation. [Thesis]. University of Illinois – Chicago; 2012. Available from: http://hdl.handle.net/10027/9243

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


University of Toronto

28. Magomedova, Lilia. Identification and Characterization of ARGLU1, a Novel Glucocorticoid Receptor Coactivator.

Degree: PhD, 2016, University of Toronto

Glucocorticoids (GCs) are stress-induced hormones that signal to multiple tissues in the body to increase glucose levels in circulation. Prolonged GC stimulation, however, leads to… (more)

Subjects/Keywords: Coactivators; Diabetes; Glucocorticoids; Nuclear receptors; Obesity; Splicing; 0572

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

APA (6th Edition):

Magomedova, L. (2016). Identification and Characterization of ARGLU1, a Novel Glucocorticoid Receptor Coactivator. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/89272

Chicago Manual of Style (16th Edition):

Magomedova, Lilia. “Identification and Characterization of ARGLU1, a Novel Glucocorticoid Receptor Coactivator.” 2016. Doctoral Dissertation, University of Toronto. Accessed October 22, 2020. http://hdl.handle.net/1807/89272.

MLA Handbook (7th Edition):

Magomedova, Lilia. “Identification and Characterization of ARGLU1, a Novel Glucocorticoid Receptor Coactivator.” 2016. Web. 22 Oct 2020.

Vancouver:

Magomedova L. Identification and Characterization of ARGLU1, a Novel Glucocorticoid Receptor Coactivator. [Internet] [Doctoral dissertation]. University of Toronto; 2016. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/1807/89272.

Council of Science Editors:

Magomedova L. Identification and Characterization of ARGLU1, a Novel Glucocorticoid Receptor Coactivator. [Doctoral Dissertation]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/89272


University of Toronto

29. Patel, Rucha. Molecular Regulation of Gluconeogenesis by the Nuclear Receptors GR and LXRβ.

Degree: PhD, 2015, University of Toronto

The long-term use of immunosuppressive glucocorticoid (GC) drugs is limited by undesirable side effects including osteoporosis, obesity, and type 2 diabetes. The potent induction of… (more)

Subjects/Keywords: ChIP; Gene regulation; Glucocorticoids; Gluconeogenesis; lipogenesis; Nuclear receptors; 0306

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

APA (6th Edition):

Patel, R. (2015). Molecular Regulation of Gluconeogenesis by the Nuclear Receptors GR and LXRβ. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/77717

Chicago Manual of Style (16th Edition):

Patel, Rucha. “Molecular Regulation of Gluconeogenesis by the Nuclear Receptors GR and LXRβ.” 2015. Doctoral Dissertation, University of Toronto. Accessed October 22, 2020. http://hdl.handle.net/1807/77717.

MLA Handbook (7th Edition):

Patel, Rucha. “Molecular Regulation of Gluconeogenesis by the Nuclear Receptors GR and LXRβ.” 2015. Web. 22 Oct 2020.

Vancouver:

Patel R. Molecular Regulation of Gluconeogenesis by the Nuclear Receptors GR and LXRβ. [Internet] [Doctoral dissertation]. University of Toronto; 2015. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/1807/77717.

Council of Science Editors:

Patel R. Molecular Regulation of Gluconeogenesis by the Nuclear Receptors GR and LXRβ. [Doctoral Dissertation]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/77717


University of Illinois – Urbana-Champaign

30. Charn, Tze Howe. An integrated network of estrogen receptors alpha and beta, and coregulators, for deciphering estrogen signaling in breast cancer cells.

Degree: PhD, 0408, 2011, University of Illinois – Urbana-Champaign

 The nuclear hormone receptors, ER?? and ER??, are known to regulate the transcriptional response programs of their target cells, including breast cancer cells. However, their… (more)

Subjects/Keywords: Estrogen receptors; MCF-7; nuclear receptor coactivator 3 (SRC3); RIP140

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

APA (6th Edition):

Charn, T. H. (2011). An integrated network of estrogen receptors alpha and beta, and coregulators, for deciphering estrogen signaling in breast cancer cells. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/18589

Chicago Manual of Style (16th Edition):

Charn, Tze Howe. “An integrated network of estrogen receptors alpha and beta, and coregulators, for deciphering estrogen signaling in breast cancer cells.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed October 22, 2020. http://hdl.handle.net/2142/18589.

MLA Handbook (7th Edition):

Charn, Tze Howe. “An integrated network of estrogen receptors alpha and beta, and coregulators, for deciphering estrogen signaling in breast cancer cells.” 2011. Web. 22 Oct 2020.

Vancouver:

Charn TH. An integrated network of estrogen receptors alpha and beta, and coregulators, for deciphering estrogen signaling in breast cancer cells. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/2142/18589.

Council of Science Editors:

Charn TH. An integrated network of estrogen receptors alpha and beta, and coregulators, for deciphering estrogen signaling in breast cancer cells. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/18589

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