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You searched for subject:(Pregnane X receptor). Showing records 1 – 23 of 23 total matches.

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Texas A&M University

1. Eagleton, Navada Lorraine. Novel Functions for the Pregnane X Receptor include Regulation of mRNA Turnover and Involvement in Colon Cancer Progression.

Degree: MS, Toxicology, 2011, Texas A&M University

 To understand the mechanisms of transcriptional regulation of PXR, we performed yeast two-hybrid screenings to search for PXR-interacting proteins in a human liver cDNA library… (more)

Subjects/Keywords: pregnane X receptor; PXR; CNOT2; colon cancer

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APA (6th Edition):

Eagleton, N. L. (2011). Novel Functions for the Pregnane X Receptor include Regulation of mRNA Turnover and Involvement in Colon Cancer Progression. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8029

Chicago Manual of Style (16th Edition):

Eagleton, Navada Lorraine. “Novel Functions for the Pregnane X Receptor include Regulation of mRNA Turnover and Involvement in Colon Cancer Progression.” 2011. Masters Thesis, Texas A&M University. Accessed November 27, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8029.

MLA Handbook (7th Edition):

Eagleton, Navada Lorraine. “Novel Functions for the Pregnane X Receptor include Regulation of mRNA Turnover and Involvement in Colon Cancer Progression.” 2011. Web. 27 Nov 2020.

Vancouver:

Eagleton NL. Novel Functions for the Pregnane X Receptor include Regulation of mRNA Turnover and Involvement in Colon Cancer Progression. [Internet] [Masters thesis]. Texas A&M University; 2011. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8029.

Council of Science Editors:

Eagleton NL. Novel Functions for the Pregnane X Receptor include Regulation of mRNA Turnover and Involvement in Colon Cancer Progression. [Masters Thesis]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8029

2. Xu, Chenshu. REGULATION OF DRUG METABOLISM AND INFLAMMATION BY PREGNANE X RECEPTOR.

Degree: PhD, Pharmacology & Toxicology, 2011, University of Kansas

 Liver-enriched nuclear receptor (NR) proteins regulate the expression and activity of several pivotal hepatic biochemical pathways including the uptake, metabolism and excretion of cholesterol, bile… (more)

Subjects/Keywords: Pharmacology; Toxicology; Carboxylesterase; Constitutive androstane receptor; Inflammation; Pregnane x receptor; Sumoylation

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APA (6th Edition):

Xu, C. (2011). REGULATION OF DRUG METABOLISM AND INFLAMMATION BY PREGNANE X RECEPTOR. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/9708

Chicago Manual of Style (16th Edition):

Xu, Chenshu. “REGULATION OF DRUG METABOLISM AND INFLAMMATION BY PREGNANE X RECEPTOR.” 2011. Doctoral Dissertation, University of Kansas. Accessed November 27, 2020. http://hdl.handle.net/1808/9708.

MLA Handbook (7th Edition):

Xu, Chenshu. “REGULATION OF DRUG METABOLISM AND INFLAMMATION BY PREGNANE X RECEPTOR.” 2011. Web. 27 Nov 2020.

Vancouver:

Xu C. REGULATION OF DRUG METABOLISM AND INFLAMMATION BY PREGNANE X RECEPTOR. [Internet] [Doctoral dissertation]. University of Kansas; 2011. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1808/9708.

Council of Science Editors:

Xu C. REGULATION OF DRUG METABOLISM AND INFLAMMATION BY PREGNANE X RECEPTOR. [Doctoral Dissertation]. University of Kansas; 2011. Available from: http://hdl.handle.net/1808/9708


University of Toronto

3. Hunter, Sarah Rachel. Induction of the Rat Hepatic Aryl Hydrocarbon Receptor Nuclear Translocator by Glucocorticoids.

Degree: 2014, University of Toronto

The aryl hydrocarbon receptor (AHR) nuclear translocator (ARNT), a partner in the hypoxia and AHR signaling pathways, is induced in rat liver by dexamethasone (DEX),… (more)

Subjects/Keywords: aryl hydrocarbon receptor nuclear translocator; glucocorticoid receptor; glucocorticoids; pregnane X receptor; rat; signaling pathway; 0419

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APA (6th Edition):

Hunter, S. R. (2014). Induction of the Rat Hepatic Aryl Hydrocarbon Receptor Nuclear Translocator by Glucocorticoids. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/73165

Chicago Manual of Style (16th Edition):

Hunter, Sarah Rachel. “Induction of the Rat Hepatic Aryl Hydrocarbon Receptor Nuclear Translocator by Glucocorticoids.” 2014. Masters Thesis, University of Toronto. Accessed November 27, 2020. http://hdl.handle.net/1807/73165.

MLA Handbook (7th Edition):

Hunter, Sarah Rachel. “Induction of the Rat Hepatic Aryl Hydrocarbon Receptor Nuclear Translocator by Glucocorticoids.” 2014. Web. 27 Nov 2020.

Vancouver:

Hunter SR. Induction of the Rat Hepatic Aryl Hydrocarbon Receptor Nuclear Translocator by Glucocorticoids. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1807/73165.

Council of Science Editors:

Hunter SR. Induction of the Rat Hepatic Aryl Hydrocarbon Receptor Nuclear Translocator by Glucocorticoids. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/73165

4. Breuker, Cyril. Etude des xénorécepteurs CAR (NR1I3) et PXR (NR1I2) : identification d’un nouveau gène cible de CAR (SPOT14) et d’une nouvelle isoforme de PXR (PXR-small) dans l'hépatocyte humain : Study of the CAR (NR1I3) and PXR (NR1I2) : identification of a new CAR target gene (SPOT14) and a new PXR isoform (PXR-small) in human hepatocyte.

Degree: Docteur es, Sciences du médicament, 2010, Université Montpellier I

CAR (Constitutive Androstane Receptor, NR1I3) et PXR (Pregnane X Receptor, NR1I2) sont deux récepteurs nucléaires dédiés à la reconna issance et à l'élimination de molécules… (more)

Subjects/Keywords: Récepteur nucléaire; Pregnane X Receptor; Constitutive Androstane Receptor; Métabolisme des médicaments; Perturbateur métabolique; Nuclear receptor; Pregnane X Receptor; Constitutive Androstane Receptor; Drugs metabolism; Metabolic disruptive

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APA (6th Edition):

Breuker, C. (2010). Etude des xénorécepteurs CAR (NR1I3) et PXR (NR1I2) : identification d’un nouveau gène cible de CAR (SPOT14) et d’une nouvelle isoforme de PXR (PXR-small) dans l'hépatocyte humain : Study of the CAR (NR1I3) and PXR (NR1I2) : identification of a new CAR target gene (SPOT14) and a new PXR isoform (PXR-small) in human hepatocyte. (Doctoral Dissertation). Université Montpellier I. Retrieved from http://www.theses.fr/2010MON13522

Chicago Manual of Style (16th Edition):

Breuker, Cyril. “Etude des xénorécepteurs CAR (NR1I3) et PXR (NR1I2) : identification d’un nouveau gène cible de CAR (SPOT14) et d’une nouvelle isoforme de PXR (PXR-small) dans l'hépatocyte humain : Study of the CAR (NR1I3) and PXR (NR1I2) : identification of a new CAR target gene (SPOT14) and a new PXR isoform (PXR-small) in human hepatocyte.” 2010. Doctoral Dissertation, Université Montpellier I. Accessed November 27, 2020. http://www.theses.fr/2010MON13522.

MLA Handbook (7th Edition):

Breuker, Cyril. “Etude des xénorécepteurs CAR (NR1I3) et PXR (NR1I2) : identification d’un nouveau gène cible de CAR (SPOT14) et d’une nouvelle isoforme de PXR (PXR-small) dans l'hépatocyte humain : Study of the CAR (NR1I3) and PXR (NR1I2) : identification of a new CAR target gene (SPOT14) and a new PXR isoform (PXR-small) in human hepatocyte.” 2010. Web. 27 Nov 2020.

Vancouver:

Breuker C. Etude des xénorécepteurs CAR (NR1I3) et PXR (NR1I2) : identification d’un nouveau gène cible de CAR (SPOT14) et d’une nouvelle isoforme de PXR (PXR-small) dans l'hépatocyte humain : Study of the CAR (NR1I3) and PXR (NR1I2) : identification of a new CAR target gene (SPOT14) and a new PXR isoform (PXR-small) in human hepatocyte. [Internet] [Doctoral dissertation]. Université Montpellier I; 2010. [cited 2020 Nov 27]. Available from: http://www.theses.fr/2010MON13522.

Council of Science Editors:

Breuker C. Etude des xénorécepteurs CAR (NR1I3) et PXR (NR1I2) : identification d’un nouveau gène cible de CAR (SPOT14) et d’une nouvelle isoforme de PXR (PXR-small) dans l'hépatocyte humain : Study of the CAR (NR1I3) and PXR (NR1I2) : identification of a new CAR target gene (SPOT14) and a new PXR isoform (PXR-small) in human hepatocyte. [Doctoral Dissertation]. Université Montpellier I; 2010. Available from: http://www.theses.fr/2010MON13522

5. Leguelinel, Géraldine. Rôle des récepteurs des xénobiotiques CAR (Constitutive Androstane Receptor, NR1I3) et PXR (Pregnane X receptor, NR1I2) dans le métabolisme des chimiothérapies conventionnelles du cancer colorectal : Role of xenoreceptors CAR (Constitutive Androstane Receptor, NR1I3) and PXR (Pregnane X Receptor, NR1I2) in the metabolism of conventionnal chemotherapy in colorectal cancer.

Degree: Docteur es, Biologie Santé, 2011, Université Montpellier I

Le cancer colorectal est marqué par une importante mortalité dans les stades avancés du fait du fort taux de récidives tumorales après chimiothérapie. La prédiction… (more)

Subjects/Keywords: Xénorécepteurs; Métabolisme intratumoral; Cancer colorectal; Chimiosensibilité; Constitutive Androstane Receptor; Pregnane X Receptor; Xenoreceptors; Intratumoral metabolism; Colorectal cancer; Chemosensibility; Constitutive Androstane Receptor; Pregnane X Receptor

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APA (6th Edition):

Leguelinel, G. (2011). Rôle des récepteurs des xénobiotiques CAR (Constitutive Androstane Receptor, NR1I3) et PXR (Pregnane X receptor, NR1I2) dans le métabolisme des chimiothérapies conventionnelles du cancer colorectal : Role of xenoreceptors CAR (Constitutive Androstane Receptor, NR1I3) and PXR (Pregnane X Receptor, NR1I2) in the metabolism of conventionnal chemotherapy in colorectal cancer. (Doctoral Dissertation). Université Montpellier I. Retrieved from http://www.theses.fr/2011MON13512

Chicago Manual of Style (16th Edition):

Leguelinel, Géraldine. “Rôle des récepteurs des xénobiotiques CAR (Constitutive Androstane Receptor, NR1I3) et PXR (Pregnane X receptor, NR1I2) dans le métabolisme des chimiothérapies conventionnelles du cancer colorectal : Role of xenoreceptors CAR (Constitutive Androstane Receptor, NR1I3) and PXR (Pregnane X Receptor, NR1I2) in the metabolism of conventionnal chemotherapy in colorectal cancer.” 2011. Doctoral Dissertation, Université Montpellier I. Accessed November 27, 2020. http://www.theses.fr/2011MON13512.

MLA Handbook (7th Edition):

Leguelinel, Géraldine. “Rôle des récepteurs des xénobiotiques CAR (Constitutive Androstane Receptor, NR1I3) et PXR (Pregnane X receptor, NR1I2) dans le métabolisme des chimiothérapies conventionnelles du cancer colorectal : Role of xenoreceptors CAR (Constitutive Androstane Receptor, NR1I3) and PXR (Pregnane X Receptor, NR1I2) in the metabolism of conventionnal chemotherapy in colorectal cancer.” 2011. Web. 27 Nov 2020.

Vancouver:

Leguelinel G. Rôle des récepteurs des xénobiotiques CAR (Constitutive Androstane Receptor, NR1I3) et PXR (Pregnane X receptor, NR1I2) dans le métabolisme des chimiothérapies conventionnelles du cancer colorectal : Role of xenoreceptors CAR (Constitutive Androstane Receptor, NR1I3) and PXR (Pregnane X Receptor, NR1I2) in the metabolism of conventionnal chemotherapy in colorectal cancer. [Internet] [Doctoral dissertation]. Université Montpellier I; 2011. [cited 2020 Nov 27]. Available from: http://www.theses.fr/2011MON13512.

Council of Science Editors:

Leguelinel G. Rôle des récepteurs des xénobiotiques CAR (Constitutive Androstane Receptor, NR1I3) et PXR (Pregnane X receptor, NR1I2) dans le métabolisme des chimiothérapies conventionnelles du cancer colorectal : Role of xenoreceptors CAR (Constitutive Androstane Receptor, NR1I3) and PXR (Pregnane X Receptor, NR1I2) in the metabolism of conventionnal chemotherapy in colorectal cancer. [Doctoral Dissertation]. Université Montpellier I; 2011. Available from: http://www.theses.fr/2011MON13512

6. Iannelli, Antonio. Lésions hépatiques induites par l'ischémie reperfusion et la NAFLD : mécanismes et protection : Liver injuries due to ischemia reperfusion and NAFLD : mechanisms and protection.

Degree: Docteur es, Sciences de l'environnement terrestre, 2010, Aix-Marseille 2

 Le pregnane X receptor (PXR) est un récepteur nucléaire associé à la réponse au stresscellulaire. Des travaux in vitro de notre groupe ont démontré que… (more)

Subjects/Keywords: Pregnane X receptor; Ischémie reperfusion; Foie; Bcl-xL; Stéatose; Stéatohépatite; Obésité; Syndrome métabolique; Bariatrique; Pregnane X receptor; Ischemia reperfusion; Liver; Bcl-xL; Steatosis; Steatohepatitis; Obesity; Metabolic syndrome; Bariatric

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APA (6th Edition):

Iannelli, A. (2010). Lésions hépatiques induites par l'ischémie reperfusion et la NAFLD : mécanismes et protection : Liver injuries due to ischemia reperfusion and NAFLD : mechanisms and protection. (Doctoral Dissertation). Aix-Marseille 2. Retrieved from http://www.theses.fr/2010AIX20659

Chicago Manual of Style (16th Edition):

Iannelli, Antonio. “Lésions hépatiques induites par l'ischémie reperfusion et la NAFLD : mécanismes et protection : Liver injuries due to ischemia reperfusion and NAFLD : mechanisms and protection.” 2010. Doctoral Dissertation, Aix-Marseille 2. Accessed November 27, 2020. http://www.theses.fr/2010AIX20659.

MLA Handbook (7th Edition):

Iannelli, Antonio. “Lésions hépatiques induites par l'ischémie reperfusion et la NAFLD : mécanismes et protection : Liver injuries due to ischemia reperfusion and NAFLD : mechanisms and protection.” 2010. Web. 27 Nov 2020.

Vancouver:

Iannelli A. Lésions hépatiques induites par l'ischémie reperfusion et la NAFLD : mécanismes et protection : Liver injuries due to ischemia reperfusion and NAFLD : mechanisms and protection. [Internet] [Doctoral dissertation]. Aix-Marseille 2; 2010. [cited 2020 Nov 27]. Available from: http://www.theses.fr/2010AIX20659.

Council of Science Editors:

Iannelli A. Lésions hépatiques induites par l'ischémie reperfusion et la NAFLD : mécanismes et protection : Liver injuries due to ischemia reperfusion and NAFLD : mechanisms and protection. [Doctoral Dissertation]. Aix-Marseille 2; 2010. Available from: http://www.theses.fr/2010AIX20659


Texas A&M University

7. Gu, Xinsheng. Regulation of cytochrome P450 3A4 gene expression through modulating pregnane X receptor transcriptional activity by NF-ꢬ aryl hydrocarbon receptor and xenobiotics.

Degree: PhD, Toxicology, 2009, Texas A&M University

 Cytochrome P450 3A4 (CYP3A4) is a key enzyme responsible for the metabolism of drugs and endogenous compounds in human liver and intestine. CYP3A4 gene expression… (more)

Subjects/Keywords: cytochrome P450 3A4; Pregnane X Receptor

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APA (6th Edition):

Gu, X. (2009). Regulation of cytochrome P450 3A4 gene expression through modulating pregnane X receptor transcriptional activity by NF-ꢬ aryl hydrocarbon receptor and xenobiotics. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-1630

Chicago Manual of Style (16th Edition):

Gu, Xinsheng. “Regulation of cytochrome P450 3A4 gene expression through modulating pregnane X receptor transcriptional activity by NF-ꢬ aryl hydrocarbon receptor and xenobiotics.” 2009. Doctoral Dissertation, Texas A&M University. Accessed November 27, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-1630.

MLA Handbook (7th Edition):

Gu, Xinsheng. “Regulation of cytochrome P450 3A4 gene expression through modulating pregnane X receptor transcriptional activity by NF-ꢬ aryl hydrocarbon receptor and xenobiotics.” 2009. Web. 27 Nov 2020.

Vancouver:

Gu X. Regulation of cytochrome P450 3A4 gene expression through modulating pregnane X receptor transcriptional activity by NF-ꢬ aryl hydrocarbon receptor and xenobiotics. [Internet] [Doctoral dissertation]. Texas A&M University; 2009. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1630.

Council of Science Editors:

Gu X. Regulation of cytochrome P450 3A4 gene expression through modulating pregnane X receptor transcriptional activity by NF-ꢬ aryl hydrocarbon receptor and xenobiotics. [Doctoral Dissertation]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1630


University of British Columbia

8. Yeung, Eugene Y. H. Activation of pregnane X receptor by Ginkgo biloba extract.

Degree: MS- MSc, Pharmaceutical Sciences, 2008, University of British Columbia

Pregnane X receptor (PXR) is a ligand-activated transcription factor that plays a role in a broad array of biological processes, including drug metabolism and transport.… (more)

Subjects/Keywords: Pregnane X receptor; Ginkgo biloba extract

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APA (6th Edition):

Yeung, E. Y. H. (2008). Activation of pregnane X receptor by Ginkgo biloba extract. (Masters Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/2688

Chicago Manual of Style (16th Edition):

Yeung, Eugene Y H. “Activation of pregnane X receptor by Ginkgo biloba extract.” 2008. Masters Thesis, University of British Columbia. Accessed November 27, 2020. http://hdl.handle.net/2429/2688.

MLA Handbook (7th Edition):

Yeung, Eugene Y H. “Activation of pregnane X receptor by Ginkgo biloba extract.” 2008. Web. 27 Nov 2020.

Vancouver:

Yeung EYH. Activation of pregnane X receptor by Ginkgo biloba extract. [Internet] [Masters thesis]. University of British Columbia; 2008. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2429/2688.

Council of Science Editors:

Yeung EYH. Activation of pregnane X receptor by Ginkgo biloba extract. [Masters Thesis]. University of British Columbia; 2008. Available from: http://hdl.handle.net/2429/2688

9. Roques, Beatrice. Bases mécanistiques des effets d'un insecticide agrovétérinaire, le fiproni, et/ou de ses métabolites sur la fonction thyroïdienne chez le rat : Mechanistic basis of the effects of an agroveterinary insecticide, the fipronil, and/or its metabolites on the thyroid function in rat.

Degree: Docteur es, Pathologie, Toxicologie, Génétique et Nutrition, 2012, Toulouse, INSA

Le fipronil, insecticide largement utilisé, est un perturbateur thyroïdien chez le rat modulant le catabolisme hépatique des hormones thyroïdiennes. Ses effets chez le mouton, considéré… (more)

Subjects/Keywords: Perturbateur endocrinien; Fipronil; Fipronil sulfone; Fonction thyroïdienne; Métabolisme hépatique; Rat; Souris transgéniques; Hépatocytes; Constitutive Androstane Receptor; Pregnane X Receptor; Endocrine disruptor; Fipronil; Fipronil sulfone; Thyroid function; Hepatic metabolism; Rat; Transgenic mice; Hepatocytes; Constitutive Androstane Receptor; Pregnane X Receptor; 613

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APA (6th Edition):

Roques, B. (2012). Bases mécanistiques des effets d'un insecticide agrovétérinaire, le fiproni, et/ou de ses métabolites sur la fonction thyroïdienne chez le rat : Mechanistic basis of the effects of an agroveterinary insecticide, the fipronil, and/or its metabolites on the thyroid function in rat. (Doctoral Dissertation). Toulouse, INSA. Retrieved from http://www.theses.fr/2012ISAT0029

Chicago Manual of Style (16th Edition):

Roques, Beatrice. “Bases mécanistiques des effets d'un insecticide agrovétérinaire, le fiproni, et/ou de ses métabolites sur la fonction thyroïdienne chez le rat : Mechanistic basis of the effects of an agroveterinary insecticide, the fipronil, and/or its metabolites on the thyroid function in rat.” 2012. Doctoral Dissertation, Toulouse, INSA. Accessed November 27, 2020. http://www.theses.fr/2012ISAT0029.

MLA Handbook (7th Edition):

Roques, Beatrice. “Bases mécanistiques des effets d'un insecticide agrovétérinaire, le fiproni, et/ou de ses métabolites sur la fonction thyroïdienne chez le rat : Mechanistic basis of the effects of an agroveterinary insecticide, the fipronil, and/or its metabolites on the thyroid function in rat.” 2012. Web. 27 Nov 2020.

Vancouver:

Roques B. Bases mécanistiques des effets d'un insecticide agrovétérinaire, le fiproni, et/ou de ses métabolites sur la fonction thyroïdienne chez le rat : Mechanistic basis of the effects of an agroveterinary insecticide, the fipronil, and/or its metabolites on the thyroid function in rat. [Internet] [Doctoral dissertation]. Toulouse, INSA; 2012. [cited 2020 Nov 27]. Available from: http://www.theses.fr/2012ISAT0029.

Council of Science Editors:

Roques B. Bases mécanistiques des effets d'un insecticide agrovétérinaire, le fiproni, et/ou de ses métabolites sur la fonction thyroïdienne chez le rat : Mechanistic basis of the effects of an agroveterinary insecticide, the fipronil, and/or its metabolites on the thyroid function in rat. [Doctoral Dissertation]. Toulouse, INSA; 2012. Available from: http://www.theses.fr/2012ISAT0029


University of Western Ontario

10. Woolsey, Sarah J. Cytochrome P450 3A4 Expression and Regulation in Non-Alcoholic Fatty Liver Disease.

Degree: 2015, University of Western Ontario

 Non-alcoholic fatty liver disease (NAFLD) is defined as lipid accumulation within hepatocytes (steatosis) in the absence of excess alcohol consumption. It is the most common… (more)

Subjects/Keywords: Non-alcoholic fatty liver disease; Cytochrome P450 3A4; Drug metabolism; Gene regulation; Fibroblast growth factor 21; Pregnane x receptor; Diseases; Pharmacology

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APA (6th Edition):

Woolsey, S. J. (2015). Cytochrome P450 3A4 Expression and Regulation in Non-Alcoholic Fatty Liver Disease. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/3355

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):

Woolsey, Sarah J. “Cytochrome P450 3A4 Expression and Regulation in Non-Alcoholic Fatty Liver Disease.” 2015. Thesis, University of Western Ontario. Accessed November 27, 2020. https://ir.lib.uwo.ca/etd/3355.

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

MLA Handbook (7th Edition):

Woolsey, Sarah J. “Cytochrome P450 3A4 Expression and Regulation in Non-Alcoholic Fatty Liver Disease.” 2015. Web. 27 Nov 2020.

Vancouver:

Woolsey SJ. Cytochrome P450 3A4 Expression and Regulation in Non-Alcoholic Fatty Liver Disease. [Internet] [Thesis]. University of Western Ontario; 2015. [cited 2020 Nov 27]. Available from: https://ir.lib.uwo.ca/etd/3355.

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

Council of Science Editors:

Woolsey SJ. Cytochrome P450 3A4 Expression and Regulation in Non-Alcoholic Fatty Liver Disease. [Thesis]. University of Western Ontario; 2015. Available from: https://ir.lib.uwo.ca/etd/3355

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


University of Western Ontario

11. Wilson, Aze. Drug Response And Metabolism In Crohn's Disease.

Degree: 2018, University of Western Ontario

 Inflammatory bowel disease (IBD) is an illness of chronic intestinal inflammation comprised of Crohn's disease (CD) and ulcerative colitis (UC). Specialists rely heavily on drugs… (more)

Subjects/Keywords: Crohn's disease; drug metabolism; farnesoid X receptor; pregnane X receptor; cytochrome P450 3A4; pharmacokinetics; Digestive System Diseases; Gastroenterology; Medical Pharmacology; Medicine and Health Sciences; Translational Medical Research

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APA (6th Edition):

Wilson, A. (2018). Drug Response And Metabolism In Crohn's Disease. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/5557

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):

Wilson, Aze. “Drug Response And Metabolism In Crohn's Disease.” 2018. Thesis, University of Western Ontario. Accessed November 27, 2020. https://ir.lib.uwo.ca/etd/5557.

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

MLA Handbook (7th Edition):

Wilson, Aze. “Drug Response And Metabolism In Crohn's Disease.” 2018. Web. 27 Nov 2020.

Vancouver:

Wilson A. Drug Response And Metabolism In Crohn's Disease. [Internet] [Thesis]. University of Western Ontario; 2018. [cited 2020 Nov 27]. Available from: https://ir.lib.uwo.ca/etd/5557.

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

Council of Science Editors:

Wilson A. Drug Response And Metabolism In Crohn's Disease. [Thesis]. University of Western Ontario; 2018. Available from: https://ir.lib.uwo.ca/etd/5557

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

12. Richter, Ingrid. Molecular evolution and functional characterisation of tunicate xenobiotic receptors.

Degree: 2015, Victoria University of Wellington

 Marine microorganisms generate a wide range of ’bioactive’ compounds that can have far-reaching effects on biological and ecological processes. Metazoans have developed specialised biochemical pathways… (more)

Subjects/Keywords: Yeast bioassay; PXR; Pregnane X receptor; Molecular evolution

…tunicate orthologues of the pregnane X receptor (PXR): characterisation and natural… …11 Pectenotoxin-11 PXR Pregnane X receptor qPCR Quantitative polymerase chain reaction… …domains (DBDs) and ligand-binding domains (LBDs) from pregnane X receptor… …Appendix Four: 204 Amplification of Ciona intestinalis vitamin D receptor/pregnane X receptor α… …for the expression of Ciona intestinalis vitamin D receptor/pregnane X receptor α (… 

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APA (6th Edition):

Richter, I. (2015). Molecular evolution and functional characterisation of tunicate xenobiotic receptors. (Doctoral Dissertation). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/4652

Chicago Manual of Style (16th Edition):

Richter, Ingrid. “Molecular evolution and functional characterisation of tunicate xenobiotic receptors.” 2015. Doctoral Dissertation, Victoria University of Wellington. Accessed November 27, 2020. http://hdl.handle.net/10063/4652.

MLA Handbook (7th Edition):

Richter, Ingrid. “Molecular evolution and functional characterisation of tunicate xenobiotic receptors.” 2015. Web. 27 Nov 2020.

Vancouver:

Richter I. Molecular evolution and functional characterisation of tunicate xenobiotic receptors. [Internet] [Doctoral dissertation]. Victoria University of Wellington; 2015. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10063/4652.

Council of Science Editors:

Richter I. Molecular evolution and functional characterisation of tunicate xenobiotic receptors. [Doctoral Dissertation]. Victoria University of Wellington; 2015. Available from: http://hdl.handle.net/10063/4652

13. Lichti-Kaiser, Kristin Nicole. Regulation of the Pregnane X Receptor Signaling Pathway.

Degree: PhD, Pharmacology & Toxicology, 2009, University of Kansas

 Liver-enriched nuclear receptors (NRs) collectively function as metabolic and toxicological `sensors' that mediate liver-specific gene-activation in mammals. NR-mediated gene-environment interaction regulates important steps in the… (more)

Subjects/Keywords: Health sciences; Pharmacology; Cell signaling; Gene expression; Pregnane x receptor

Pregnane X Receptor PXR-KO: Pregnane X Receptor Knockout RAR: Retinoic Acid Receptor RIF… …and may affect the function of PPARα as a drug target. 1.2.3 NR1I2, PXR Pregnane x receptor… …LPS: Lipopolysaccharide LRH-1: Liver Receptor Homolog 1 LXR: Liver X Receptor MAPK: Mitogen… …Rifampicin ROS: Reactive Oxygen Species RXR: Retinoid X Receptor ix SCD1: Stearoyl-CoA… …Glucuronosyltransferase VDR: Vitamin D Receptor XREM: Xenobiotic Responsive Enhancer Module x Table of… 

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APA (6th Edition):

Lichti-Kaiser, K. N. (2009). Regulation of the Pregnane X Receptor Signaling Pathway. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/6188

Chicago Manual of Style (16th Edition):

Lichti-Kaiser, Kristin Nicole. “Regulation of the Pregnane X Receptor Signaling Pathway.” 2009. Doctoral Dissertation, University of Kansas. Accessed November 27, 2020. http://hdl.handle.net/1808/6188.

MLA Handbook (7th Edition):

Lichti-Kaiser, Kristin Nicole. “Regulation of the Pregnane X Receptor Signaling Pathway.” 2009. Web. 27 Nov 2020.

Vancouver:

Lichti-Kaiser KN. Regulation of the Pregnane X Receptor Signaling Pathway. [Internet] [Doctoral dissertation]. University of Kansas; 2009. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1808/6188.

Council of Science Editors:

Lichti-Kaiser KN. Regulation of the Pregnane X Receptor Signaling Pathway. [Doctoral Dissertation]. University of Kansas; 2009. Available from: http://hdl.handle.net/1808/6188


University of Oslo

14. Tapia, German. Regulation of ABCA1 in hepatocytes by the nuclear receptor PXR.

Degree: 2005, University of Oslo

 Abstract Nuclear receptors that work as heterodimers with RXR control several aspects of lipid metabolism. One such nuclear receptor, pregnane X receptor (PXR) is the… (more)

Subjects/Keywords: molekylærbiologi ABCA1 kolesterol lever PKR pregnane X-receptor atherosclerosis åreforkalkning; VDP::476

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APA (6th Edition):

Tapia, G. (2005). Regulation of ABCA1 in hepatocytes by the nuclear receptor PXR. (Thesis). University of Oslo. Retrieved from http://urn.nb.no/URN:NBN:no-11209 ; https://www.duo.uio.no/handle/10852/11364 ; Fulltext https://www.duo.uio.no/bitstream/handle/10852/11364/2/Masteroppgave.pdf

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):

Tapia, German. “Regulation of ABCA1 in hepatocytes by the nuclear receptor PXR.” 2005. Thesis, University of Oslo. Accessed November 27, 2020. http://urn.nb.no/URN:NBN:no-11209 ; https://www.duo.uio.no/handle/10852/11364 ; Fulltext https://www.duo.uio.no/bitstream/handle/10852/11364/2/Masteroppgave.pdf.

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

MLA Handbook (7th Edition):

Tapia, German. “Regulation of ABCA1 in hepatocytes by the nuclear receptor PXR.” 2005. Web. 27 Nov 2020.

Vancouver:

Tapia G. Regulation of ABCA1 in hepatocytes by the nuclear receptor PXR. [Internet] [Thesis]. University of Oslo; 2005. [cited 2020 Nov 27]. Available from: http://urn.nb.no/URN:NBN:no-11209 ; https://www.duo.uio.no/handle/10852/11364 ; Fulltext https://www.duo.uio.no/bitstream/handle/10852/11364/2/Masteroppgave.pdf.

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

Council of Science Editors:

Tapia G. Regulation of ABCA1 in hepatocytes by the nuclear receptor PXR. [Thesis]. University of Oslo; 2005. Available from: http://urn.nb.no/URN:NBN:no-11209 ; https://www.duo.uio.no/handle/10852/11364 ; Fulltext https://www.duo.uio.no/bitstream/handle/10852/11364/2/Masteroppgave.pdf

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


RMIT University

15. Liu, Y. A bioinformatic and cell-based study on the mutation and regulation of human nuclear receptors and their target genes.

Degree: 2010, RMIT University

 Human nuclear receptor (NR) superfamily represents an important group of regulating factors of a large number of physiologically important target genes. In this project, we… (more)

Subjects/Keywords: Fields of Research; Nuclear Receptor; Pregnane X Receptor (PXR); Cytochrome P450 3A4 (CYP3A4); Single Nucleotide Polymorphism (SNP); non-synonymous SNP; ATP-Binding Cassette (ABC) Transporters; Sorting Intolerant from Tolerant (SIFT); Polymorphism Phenotyping (PolyPhen); Target Gene; Chinese Herbal Medicine; Herb-Drug Interaction

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APA (6th Edition):

Liu, Y. (2010). A bioinformatic and cell-based study on the mutation and regulation of human nuclear receptors and their target genes. (Thesis). RMIT University. Retrieved from http://researchbank.rmit.edu.au/view/rmit:160620

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):

Liu, Y. “A bioinformatic and cell-based study on the mutation and regulation of human nuclear receptors and their target genes.” 2010. Thesis, RMIT University. Accessed November 27, 2020. http://researchbank.rmit.edu.au/view/rmit:160620.

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

MLA Handbook (7th Edition):

Liu, Y. “A bioinformatic and cell-based study on the mutation and regulation of human nuclear receptors and their target genes.” 2010. Web. 27 Nov 2020.

Vancouver:

Liu Y. A bioinformatic and cell-based study on the mutation and regulation of human nuclear receptors and their target genes. [Internet] [Thesis]. RMIT University; 2010. [cited 2020 Nov 27]. Available from: http://researchbank.rmit.edu.au/view/rmit:160620.

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

Council of Science Editors:

Liu Y. A bioinformatic and cell-based study on the mutation and regulation of human nuclear receptors and their target genes. [Thesis]. RMIT University; 2010. Available from: http://researchbank.rmit.edu.au/view/rmit:160620

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


North Carolina State University

16. Jackson, Jonathan Patrick. The Role of the Nuclear Receptors CAR and PXR in the Drug Induced Transcriptional Regulation of the Murine CYP2C Subfamily of Cytochrome P450 Monooxygenases.

Degree: PhD, Toxicology, 2007, North Carolina State University

 The CYP2C subfamily of cytochrome P450 monoxygenases (P450) is responsible for the metabolism of approximately 20% of therapeutic drugs. Recently, phenytoin has been reported to… (more)

Subjects/Keywords: Cyp2c37; Cyp2c29; Nuclear Receptors; Pregnane X Receptor; Constitutive Androstane Receptor; Phenytoin; Phenobarbital; Drug Induction

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APA (6th Edition):

Jackson, J. P. (2007). The Role of the Nuclear Receptors CAR and PXR in the Drug Induced Transcriptional Regulation of the Murine CYP2C Subfamily of Cytochrome P450 Monooxygenases. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/4828

Chicago Manual of Style (16th Edition):

Jackson, Jonathan Patrick. “The Role of the Nuclear Receptors CAR and PXR in the Drug Induced Transcriptional Regulation of the Murine CYP2C Subfamily of Cytochrome P450 Monooxygenases.” 2007. Doctoral Dissertation, North Carolina State University. Accessed November 27, 2020. http://www.lib.ncsu.edu/resolver/1840.16/4828.

MLA Handbook (7th Edition):

Jackson, Jonathan Patrick. “The Role of the Nuclear Receptors CAR and PXR in the Drug Induced Transcriptional Regulation of the Murine CYP2C Subfamily of Cytochrome P450 Monooxygenases.” 2007. Web. 27 Nov 2020.

Vancouver:

Jackson JP. The Role of the Nuclear Receptors CAR and PXR in the Drug Induced Transcriptional Regulation of the Murine CYP2C Subfamily of Cytochrome P450 Monooxygenases. [Internet] [Doctoral dissertation]. North Carolina State University; 2007. [cited 2020 Nov 27]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/4828.

Council of Science Editors:

Jackson JP. The Role of the Nuclear Receptors CAR and PXR in the Drug Induced Transcriptional Regulation of the Murine CYP2C Subfamily of Cytochrome P450 Monooxygenases. [Doctoral Dissertation]. North Carolina State University; 2007. Available from: http://www.lib.ncsu.edu/resolver/1840.16/4828


Indian Institute of Science

17. Dighe, Anasuya. Studies on Dynamic Plasticity of Ligand Binding Sites in Proteins.

Degree: PhD, Faculty of Science, 2019, Indian Institute of Science

 Molecular recognition between proteins and their associated ligands constitutes ligand-induced protein rewiring thereby enabling the formation of a stable protein-ligand complex. The studies presented in… (more)

Subjects/Keywords: Protein-ligand Interactions; Protein Ligand Interactions; Protein Structure Networks (PSNs); Graph Theory; Protein Side-chain Networks (PScN); Muscarinic Acetylcholine Receptors; Muscarinic Receptor Cmplexes; Protein-Protein Interactions; Pregnane X Receptor; G-Protein Coupled Receptors (GPCRs); Network Similarity Score (NSS); Biochemistry

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APA (6th Edition):

Dighe, A. (2019). Studies on Dynamic Plasticity of Ligand Binding Sites in Proteins. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/4236

Chicago Manual of Style (16th Edition):

Dighe, Anasuya. “Studies on Dynamic Plasticity of Ligand Binding Sites in Proteins.” 2019. Doctoral Dissertation, Indian Institute of Science. Accessed November 27, 2020. http://etd.iisc.ac.in/handle/2005/4236.

MLA Handbook (7th Edition):

Dighe, Anasuya. “Studies on Dynamic Plasticity of Ligand Binding Sites in Proteins.” 2019. Web. 27 Nov 2020.

Vancouver:

Dighe A. Studies on Dynamic Plasticity of Ligand Binding Sites in Proteins. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2019. [cited 2020 Nov 27]. Available from: http://etd.iisc.ac.in/handle/2005/4236.

Council of Science Editors:

Dighe A. Studies on Dynamic Plasticity of Ligand Binding Sites in Proteins. [Doctoral Dissertation]. Indian Institute of Science; 2019. Available from: http://etd.iisc.ac.in/handle/2005/4236


University of Kansas

18. Pacyniak, Erik Kristofer. Molecular Mechanism of Polybrominated Diphenyl Ether Disposition in the Liver.

Degree: PhD, Pharmacology, Toxicology & Therapeutics, 2010, University of Kansas

 Polybrominated diphenyl ethers (PBDEs) were introduced in the late 1970's as additive flame retardants incorporated into textiles, electronics, plastics and furniture. Although 2,2',3,3',4,4',5,5',6,6'-decabromodiphenyl ether (BDE209)… (more)

Subjects/Keywords: Toxicology; Constitutive androstane receptor; Nuclear receptors; Organic anion transporting polypeptide; Polybrominated diphenyl ethers; Pregnane x receptor

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APA (6th Edition):

Pacyniak, E. K. (2010). Molecular Mechanism of Polybrominated Diphenyl Ether Disposition in the Liver. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/7717

Chicago Manual of Style (16th Edition):

Pacyniak, Erik Kristofer. “Molecular Mechanism of Polybrominated Diphenyl Ether Disposition in the Liver.” 2010. Doctoral Dissertation, University of Kansas. Accessed November 27, 2020. http://hdl.handle.net/1808/7717.

MLA Handbook (7th Edition):

Pacyniak, Erik Kristofer. “Molecular Mechanism of Polybrominated Diphenyl Ether Disposition in the Liver.” 2010. Web. 27 Nov 2020.

Vancouver:

Pacyniak EK. Molecular Mechanism of Polybrominated Diphenyl Ether Disposition in the Liver. [Internet] [Doctoral dissertation]. University of Kansas; 2010. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1808/7717.

Council of Science Editors:

Pacyniak EK. Molecular Mechanism of Polybrominated Diphenyl Ether Disposition in the Liver. [Doctoral Dissertation]. University of Kansas; 2010. Available from: http://hdl.handle.net/1808/7717


University of Oulu

19. Käräjämäki, A. (Aki). Non-alcoholic fatty liver disease (NAFLD):perspectives to etiology, complications and lipid metabolism.

Degree: 2017, University of Oulu

Abstract Obesity, insulin resistance, type 2 diabetes (T2D) and non-alcoholic fatty liver disease (NAFLD) form a dangerous quartet which threatens human health all over the… (more)

Subjects/Keywords: atrial fibrillation; cardiovascular diseases; liver fibrosis; non-alcoholic fatty liver disease; pregnane X receptor; type 2 diabetes; alkoholin käyttöön liittymätön rasvamaksa; eteisvärinä; maksafibroosi; pregnaani X reseptori; sydän- ja verisuonisairaudet; tyypin 2 diabetes

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APA (6th Edition):

Käräjämäki, A. (. (2017). Non-alcoholic fatty liver disease (NAFLD):perspectives to etiology, complications and lipid metabolism. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789526217376

Chicago Manual of Style (16th Edition):

Käräjämäki, A (Aki). “Non-alcoholic fatty liver disease (NAFLD):perspectives to etiology, complications and lipid metabolism.” 2017. Doctoral Dissertation, University of Oulu. Accessed November 27, 2020. http://urn.fi/urn:isbn:9789526217376.

MLA Handbook (7th Edition):

Käräjämäki, A (Aki). “Non-alcoholic fatty liver disease (NAFLD):perspectives to etiology, complications and lipid metabolism.” 2017. Web. 27 Nov 2020.

Vancouver:

Käräjämäki A(. Non-alcoholic fatty liver disease (NAFLD):perspectives to etiology, complications and lipid metabolism. [Internet] [Doctoral dissertation]. University of Oulu; 2017. [cited 2020 Nov 27]. Available from: http://urn.fi/urn:isbn:9789526217376.

Council of Science Editors:

Käräjämäki A(. Non-alcoholic fatty liver disease (NAFLD):perspectives to etiology, complications and lipid metabolism. [Doctoral Dissertation]. University of Oulu; 2017. Available from: http://urn.fi/urn:isbn:9789526217376

20. Shaffer, Hally A. Engineering the pregnane X receptor and estrogen receptor alpha to bind novel small molecules using negative chemical complementation.

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

 Nuclear receptors are ligand-activated transcription factors that play significant roles in various biological processes within the body, such as cell development, hormone metabolism, reproduction, and… (more)

Subjects/Keywords: Nuclear receptors; Chemical complementation; Negative chemical complementation; Yeast-two hybrid selection; Pregnane X receptor; Estrogen receptor; Pregnane; Protein engineering; Nuclear receptors (Biochemistry); Transcription factors; Yeast Genetics

…ANTIBIOTICS: PREGNANE X RECEPTOR 27 2.1 Engineering Nuclear Receptors to Bind Antibiotics 27 2.2… …galactopyranoside ONPG PDB Protein Data Bank xvii PXR Pregnane X Receptor RE Response Element… …activate transcription in response to the β-lactam antibiotics was the pregnane X receptor (… …Ligand-binding Domain LXR Liver X Receptor MR Mineralocorticoid Receptor o-nitrophenyl β-D… …RNAP RNA Polymerase RXR Retinoid X Receptor SERM Selective Estrogen Receptor Modulator… 

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APA (6th Edition):

Shaffer, H. A. (2011). Engineering the pregnane X receptor and estrogen receptor alpha to bind novel small molecules using negative chemical complementation. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/39620

Chicago Manual of Style (16th Edition):

Shaffer, Hally A. “Engineering the pregnane X receptor and estrogen receptor alpha to bind novel small molecules using negative chemical complementation.” 2011. Doctoral Dissertation, Georgia Tech. Accessed November 27, 2020. http://hdl.handle.net/1853/39620.

MLA Handbook (7th Edition):

Shaffer, Hally A. “Engineering the pregnane X receptor and estrogen receptor alpha to bind novel small molecules using negative chemical complementation.” 2011. Web. 27 Nov 2020.

Vancouver:

Shaffer HA. Engineering the pregnane X receptor and estrogen receptor alpha to bind novel small molecules using negative chemical complementation. [Internet] [Doctoral dissertation]. Georgia Tech; 2011. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1853/39620.

Council of Science Editors:

Shaffer HA. Engineering the pregnane X receptor and estrogen receptor alpha to bind novel small molecules using negative chemical complementation. [Doctoral Dissertation]. Georgia Tech; 2011. Available from: http://hdl.handle.net/1853/39620

21. Helsley, Robert N. THE ROLE OF PXR AND IKKβ SIGNALING IN CARDIOMETABOLIC DISEASE.

Degree: 2016, University of Kentucky

 Cardiovascular disease (CVD) is the leading cause of death worldwide and is partially attributed to perturbations in lipid metabolism. Xenobiotics, such as pharmaceutical drugs and… (more)

Subjects/Keywords: HIV drugs; Phthalates; Pregnane X Receptor; IκB Kinase β; Adipogenesis; Insulin Resistance; Cardiovascular Diseases; Hormones, Hormone Substitutes, and Hormone Antagonists; Lipids; Medical Molecular Biology; Medical Nutrition; Medical Pharmacology; Medical Sciences; Medical Toxicology; Molecular, Genetic, and Biochemical Nutrition; Nutritional and Metabolic Diseases; Other Pharmacology, Toxicology and Environmental Health

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APA (6th Edition):

Helsley, R. N. (2016). THE ROLE OF PXR AND IKKβ SIGNALING IN CARDIOMETABOLIC DISEASE. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacol_etds/14

Chicago Manual of Style (16th Edition):

Helsley, Robert N. “THE ROLE OF PXR AND IKKβ SIGNALING IN CARDIOMETABOLIC DISEASE.” 2016. Doctoral Dissertation, University of Kentucky. Accessed November 27, 2020. https://uknowledge.uky.edu/pharmacol_etds/14.

MLA Handbook (7th Edition):

Helsley, Robert N. “THE ROLE OF PXR AND IKKβ SIGNALING IN CARDIOMETABOLIC DISEASE.” 2016. Web. 27 Nov 2020.

Vancouver:

Helsley RN. THE ROLE OF PXR AND IKKβ SIGNALING IN CARDIOMETABOLIC DISEASE. [Internet] [Doctoral dissertation]. University of Kentucky; 2016. [cited 2020 Nov 27]. Available from: https://uknowledge.uky.edu/pharmacol_etds/14.

Council of Science Editors:

Helsley RN. THE ROLE OF PXR AND IKKβ SIGNALING IN CARDIOMETABOLIC DISEASE. [Doctoral Dissertation]. University of Kentucky; 2016. Available from: https://uknowledge.uky.edu/pharmacol_etds/14

22. Touloupi, Katerina. Regulation of aldehyde dehydrogenases by nuclear receptors CAR and PXR in rats genetically predetermined in response to phenobarbital.

Degree: 2015, University of Ioannina; Πανεπιστήμιο Ιωαννίνων

The magnitude of the genes belonging to the ALDH superfamily in organism’s welfare andespecially their protection against xenobiotics, as well as the accumulating evidence that… (more)

Subjects/Keywords: Αλδεϋδικές αφυδρογονάσες 1Α1 και 1Α7; Πυρηνικοί υποδοχείς; Ιδιοσυστατικός υποδοχέας ανδροστενών; Υποδοχέας πρεγνανίου; φαινοβαρβιτάλη; Καρβονιτρίλιο της πρεγνενολόνης; Μετρήσεις γονιδίου αναφοράς; Δοκιμασίες ανοσοκαθίζησης χρωματίνης; Aldehyde dehydrogenases (ALDHs) 1A1 and 1A7; Nuclear receptors; Constitutive androstane receptor (CAR);

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APA (6th Edition):

Touloupi, K. (2015). Regulation of aldehyde dehydrogenases by nuclear receptors CAR and PXR in rats genetically predetermined in response to phenobarbital. (Thesis). University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Retrieved from http://hdl.handle.net/10442/hedi/43024

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):

Touloupi, Katerina. “Regulation of aldehyde dehydrogenases by nuclear receptors CAR and PXR in rats genetically predetermined in response to phenobarbital.” 2015. Thesis, University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Accessed November 27, 2020. http://hdl.handle.net/10442/hedi/43024.

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

MLA Handbook (7th Edition):

Touloupi, Katerina. “Regulation of aldehyde dehydrogenases by nuclear receptors CAR and PXR in rats genetically predetermined in response to phenobarbital.” 2015. Web. 27 Nov 2020.

Vancouver:

Touloupi K. Regulation of aldehyde dehydrogenases by nuclear receptors CAR and PXR in rats genetically predetermined in response to phenobarbital. [Internet] [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2015. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10442/hedi/43024.

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

Council of Science Editors:

Touloupi K. Regulation of aldehyde dehydrogenases by nuclear receptors CAR and PXR in rats genetically predetermined in response to phenobarbital. [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2015. Available from: http://hdl.handle.net/10442/hedi/43024

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


University of Cincinnati

23. Sane, Rucha S. Differential Induction of Drug Metabolizing Enzymes and Drug Transporters by Tamoxifen: Molecular Mechanisms and Clinical Implications.

Degree: PhD, Pharmacy : Pharmaceutical Sciences, 2006, University of Cincinnati

 Tamoxifen is a widely used antiestrogen in the treatment and prevention of breast cancer. Some of its unresolved problems include the occurrence of drug-drug interactions,… (more)

Subjects/Keywords: Health Sciences, General; Tamoxifen; CYP3A4; Cytochrome P450; Enzyme induction; drug metabolism; human hepatocytes; UDP-glucuronosyl transferase; P-glycoprotein; Pregnane X Receptor; PXR; LS174T

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APA (6th Edition):

Sane, R. S. (2006). Differential Induction of Drug Metabolizing Enzymes and Drug Transporters by Tamoxifen: Molecular Mechanisms and Clinical Implications. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1143410615

Chicago Manual of Style (16th Edition):

Sane, Rucha S. “Differential Induction of Drug Metabolizing Enzymes and Drug Transporters by Tamoxifen: Molecular Mechanisms and Clinical Implications.” 2006. Doctoral Dissertation, University of Cincinnati. Accessed November 27, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1143410615.

MLA Handbook (7th Edition):

Sane, Rucha S. “Differential Induction of Drug Metabolizing Enzymes and Drug Transporters by Tamoxifen: Molecular Mechanisms and Clinical Implications.” 2006. Web. 27 Nov 2020.

Vancouver:

Sane RS. Differential Induction of Drug Metabolizing Enzymes and Drug Transporters by Tamoxifen: Molecular Mechanisms and Clinical Implications. [Internet] [Doctoral dissertation]. University of Cincinnati; 2006. [cited 2020 Nov 27]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1143410615.

Council of Science Editors:

Sane RS. Differential Induction of Drug Metabolizing Enzymes and Drug Transporters by Tamoxifen: Molecular Mechanisms and Clinical Implications. [Doctoral Dissertation]. University of Cincinnati; 2006. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1143410615

.