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You searched for subject:(Glucuronidation). Showing records 1 – 28 of 28 total matches.

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Temple University

1. Okpor, Otito Iwuchukwu. SYNTHESIS AND CHARACTERIZATION OF RESVERATROL AND ITS CONJUGATED METABOLITES AND CONTRIBUTION OF METABOLISM TO ITS DECREASED BIOVAILABILITY.

Degree: PhD, 2011, Temple University

Pharmaceutical Sciences

The purported chemopreventive and chemotherapeutic properties of the dietary phytochemical resveratrol continue to undergo active investigations. Systemic pharmacokinetics of this compound revealed that… (more)

Subjects/Keywords: Pharmaceutical Sciences; Chemoprevention; Genotype-phenotype; Glucuronidation; Polyphenols; Resveratrol; UGT

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APA (6th Edition):

Okpor, O. I. (2011). SYNTHESIS AND CHARACTERIZATION OF RESVERATROL AND ITS CONJUGATED METABOLITES AND CONTRIBUTION OF METABOLISM TO ITS DECREASED BIOVAILABILITY. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,134564

Chicago Manual of Style (16th Edition):

Okpor, Otito Iwuchukwu. “SYNTHESIS AND CHARACTERIZATION OF RESVERATROL AND ITS CONJUGATED METABOLITES AND CONTRIBUTION OF METABOLISM TO ITS DECREASED BIOVAILABILITY.” 2011. Doctoral Dissertation, Temple University. Accessed May 25, 2019. http://digital.library.temple.edu/u?/p245801coll10,134564.

MLA Handbook (7th Edition):

Okpor, Otito Iwuchukwu. “SYNTHESIS AND CHARACTERIZATION OF RESVERATROL AND ITS CONJUGATED METABOLITES AND CONTRIBUTION OF METABOLISM TO ITS DECREASED BIOVAILABILITY.” 2011. Web. 25 May 2019.

Vancouver:

Okpor OI. SYNTHESIS AND CHARACTERIZATION OF RESVERATROL AND ITS CONJUGATED METABOLITES AND CONTRIBUTION OF METABOLISM TO ITS DECREASED BIOVAILABILITY. [Internet] [Doctoral dissertation]. Temple University; 2011. [cited 2019 May 25]. Available from: http://digital.library.temple.edu/u?/p245801coll10,134564.

Council of Science Editors:

Okpor OI. SYNTHESIS AND CHARACTERIZATION OF RESVERATROL AND ITS CONJUGATED METABOLITES AND CONTRIBUTION OF METABOLISM TO ITS DECREASED BIOVAILABILITY. [Doctoral Dissertation]. Temple University; 2011. Available from: http://digital.library.temple.edu/u?/p245801coll10,134564


University of Guelph

2. Laderoute, Heidi. The metabolism of androstenone and other steroid hormone conjugates in relation to boar taint .

Degree: 2015, University of Guelph

 Increased public interest in the welfare of pigs reared for pork production has led to an increased effort in finding new approaches for controlling the… (more)

Subjects/Keywords: Boar Taint; Androstenone; Sulfoconjugation; Sulfotransferase Enzymes; Glucuronidation; Enzyme Kinetics; Pig

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APA (6th Edition):

Laderoute, H. (2015). The metabolism of androstenone and other steroid hormone conjugates in relation to boar taint . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8837

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):

Laderoute, Heidi. “The metabolism of androstenone and other steroid hormone conjugates in relation to boar taint .” 2015. Thesis, University of Guelph. Accessed May 25, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8837.

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

MLA Handbook (7th Edition):

Laderoute, Heidi. “The metabolism of androstenone and other steroid hormone conjugates in relation to boar taint .” 2015. Web. 25 May 2019.

Vancouver:

Laderoute H. The metabolism of androstenone and other steroid hormone conjugates in relation to boar taint . [Internet] [Thesis]. University of Guelph; 2015. [cited 2019 May 25]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8837.

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

Council of Science Editors:

Laderoute H. The metabolism of androstenone and other steroid hormone conjugates in relation to boar taint . [Thesis]. University of Guelph; 2015. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8837

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

3. van Beusekom, C.D. van. Feline hepatic biotransformation and transport mechanisms.

Degree: 2015, Universiteit Utrecht

 Hepatic biotransformation and drug transport mechanisms vary significantly between species. While these processes that determine largely the kinetic behavior of drugs have been studied abundantly… (more)

Subjects/Keywords: cats; drug; biotransformation; toxicity; dogs; metabolism; liver; CYP450; glucuronidation; ABC-transporters

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APA (6th Edition):

van Beusekom, C. D. v. (2015). Feline hepatic biotransformation and transport mechanisms. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/308618

Chicago Manual of Style (16th Edition):

van Beusekom, C D van. “Feline hepatic biotransformation and transport mechanisms.” 2015. Doctoral Dissertation, Universiteit Utrecht. Accessed May 25, 2019. http://dspace.library.uu.nl:8080/handle/1874/308618.

MLA Handbook (7th Edition):

van Beusekom, C D van. “Feline hepatic biotransformation and transport mechanisms.” 2015. Web. 25 May 2019.

Vancouver:

van Beusekom CDv. Feline hepatic biotransformation and transport mechanisms. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2015. [cited 2019 May 25]. Available from: http://dspace.library.uu.nl:8080/handle/1874/308618.

Council of Science Editors:

van Beusekom CDv. Feline hepatic biotransformation and transport mechanisms. [Doctoral Dissertation]. Universiteit Utrecht; 2015. Available from: http://dspace.library.uu.nl:8080/handle/1874/308618


Texas State University – San Marcos

4. Bohanon, Amanda. Stability Studies of Rooperol and Analogues by In Vitro Metabolism With HPLC/MS Detection.

Degree: MS, Biochemistry, 2019, Texas State University – San Marcos

 African Potato, Hypoxis hemerocallidea, has a long history of use by the indigenous people of South Africa to treat cancer and a variety of other… (more)

Subjects/Keywords: Rooperol; Hydroxytyrosol; Glucuronidation; In vitro; Metabolism; HPLC/MS

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APA (6th Edition):

Bohanon, A. (2019). Stability Studies of Rooperol and Analogues by In Vitro Metabolism With HPLC/MS Detection. (Masters Thesis). Texas State University – San Marcos. Retrieved from https://digital.library.txstate.edu/handle/10877/8179

Chicago Manual of Style (16th Edition):

Bohanon, Amanda. “Stability Studies of Rooperol and Analogues by In Vitro Metabolism With HPLC/MS Detection.” 2019. Masters Thesis, Texas State University – San Marcos. Accessed May 25, 2019. https://digital.library.txstate.edu/handle/10877/8179.

MLA Handbook (7th Edition):

Bohanon, Amanda. “Stability Studies of Rooperol and Analogues by In Vitro Metabolism With HPLC/MS Detection.” 2019. Web. 25 May 2019.

Vancouver:

Bohanon A. Stability Studies of Rooperol and Analogues by In Vitro Metabolism With HPLC/MS Detection. [Internet] [Masters thesis]. Texas State University – San Marcos; 2019. [cited 2019 May 25]. Available from: https://digital.library.txstate.edu/handle/10877/8179.

Council of Science Editors:

Bohanon A. Stability Studies of Rooperol and Analogues by In Vitro Metabolism With HPLC/MS Detection. [Masters Thesis]. Texas State University – San Marcos; 2019. Available from: https://digital.library.txstate.edu/handle/10877/8179

5. Lloret Linares, Célia. Pharmacologie de la morphine chez les sujets obèses avant et après chirurgie de l'obésité : Pharmacology of morphine in obese subjects before and after obesity surgery.

Degree: Docteur es, Pharmacologie, 2013, Université Paris Descartes – Paris V

Au cours de cette thèse, nous montrons que l’obésité est un facteur de variabilité pharmacodynamique et pharmacocinétique de la morphine. En particulier, l’absorption et l’exposition… (more)

Subjects/Keywords: Transporteur d’efflux P-gp; Glucuronidation; Morphine; Obésité; Composition corporelle; Chirurgie bariatrique; Premier passage intestinal; Efflux transporter P-gp; Glucuronidation; Morphine; Obesity; Body Composition; Bariatric Surgery; Intestinal first-pass; 615.783

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APA (6th Edition):

Lloret Linares, C. (2013). Pharmacologie de la morphine chez les sujets obèses avant et après chirurgie de l'obésité : Pharmacology of morphine in obese subjects before and after obesity surgery. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2013PA05P627

Chicago Manual of Style (16th Edition):

Lloret Linares, Célia. “Pharmacologie de la morphine chez les sujets obèses avant et après chirurgie de l'obésité : Pharmacology of morphine in obese subjects before and after obesity surgery.” 2013. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed May 25, 2019. http://www.theses.fr/2013PA05P627.

MLA Handbook (7th Edition):

Lloret Linares, Célia. “Pharmacologie de la morphine chez les sujets obèses avant et après chirurgie de l'obésité : Pharmacology of morphine in obese subjects before and after obesity surgery.” 2013. Web. 25 May 2019.

Vancouver:

Lloret Linares C. Pharmacologie de la morphine chez les sujets obèses avant et après chirurgie de l'obésité : Pharmacology of morphine in obese subjects before and after obesity surgery. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2013. [cited 2019 May 25]. Available from: http://www.theses.fr/2013PA05P627.

Council of Science Editors:

Lloret Linares C. Pharmacologie de la morphine chez les sujets obèses avant et après chirurgie de l'obésité : Pharmacology of morphine in obese subjects before and after obesity surgery. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2013. Available from: http://www.theses.fr/2013PA05P627


University of New Orleans

6. Quadri, Syeda. Metabolomics Investigation of Glyceollins by On-Line Liquid Chromatography-Electrospray Ionization Tandem Mass Spectrometry and Fungal Metabolite Identification by Thermal Desorption Analysis Coupled with Gas Chromatography-Mass Spectrometry.

Degree: PhD, Chemistry, 2013, University of New Orleans

  Metabolomics is an emerging field that entails the detailed characterization of the ensemble of metabolites produced by living organisms; subfields include drug metabolism and… (more)

Subjects/Keywords: Glyceollins, Glucuronidation, Glutathione Conjugation, Metabolites, Phytoestrogens, Microbial Volatile Organic Compounds (MVOCs); Medicine and Health Sciences

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APA (6th Edition):

Quadri, S. (2013). Metabolomics Investigation of Glyceollins by On-Line Liquid Chromatography-Electrospray Ionization Tandem Mass Spectrometry and Fungal Metabolite Identification by Thermal Desorption Analysis Coupled with Gas Chromatography-Mass Spectrometry. (Doctoral Dissertation). University of New Orleans. Retrieved from https://scholarworks.uno.edu/td/1701

Chicago Manual of Style (16th Edition):

Quadri, Syeda. “Metabolomics Investigation of Glyceollins by On-Line Liquid Chromatography-Electrospray Ionization Tandem Mass Spectrometry and Fungal Metabolite Identification by Thermal Desorption Analysis Coupled with Gas Chromatography-Mass Spectrometry.” 2013. Doctoral Dissertation, University of New Orleans. Accessed May 25, 2019. https://scholarworks.uno.edu/td/1701.

MLA Handbook (7th Edition):

Quadri, Syeda. “Metabolomics Investigation of Glyceollins by On-Line Liquid Chromatography-Electrospray Ionization Tandem Mass Spectrometry and Fungal Metabolite Identification by Thermal Desorption Analysis Coupled with Gas Chromatography-Mass Spectrometry.” 2013. Web. 25 May 2019.

Vancouver:

Quadri S. Metabolomics Investigation of Glyceollins by On-Line Liquid Chromatography-Electrospray Ionization Tandem Mass Spectrometry and Fungal Metabolite Identification by Thermal Desorption Analysis Coupled with Gas Chromatography-Mass Spectrometry. [Internet] [Doctoral dissertation]. University of New Orleans; 2013. [cited 2019 May 25]. Available from: https://scholarworks.uno.edu/td/1701.

Council of Science Editors:

Quadri S. Metabolomics Investigation of Glyceollins by On-Line Liquid Chromatography-Electrospray Ionization Tandem Mass Spectrometry and Fungal Metabolite Identification by Thermal Desorption Analysis Coupled with Gas Chromatography-Mass Spectrometry. [Doctoral Dissertation]. University of New Orleans; 2013. Available from: https://scholarworks.uno.edu/td/1701


Université de Lorraine

7. Abbas, Suzanne. Étude des propriétés de deux séries de substances d'origine naturelle : les cucurbitacines et les parabènes : analyse de leur biotransformation chez l'homme et mesure du pouvoir cytotoxique des cucurbitacines sur une lignée cellulaire de chondrosarcome humain : Study of the properties of two series of natural derived substances : the cucurbitacins and the parabens : analysis of their biotransformation in man and measure of cucurbitacins cytotoxicity on a human chondrosarcoma cell line.

Degree: Docteur es, Sciences de la Vie et de la Santé, 2012, Université de Lorraine

Les cucurbitacines et les parabènes sont des substances d'origine naturelle appartenant à la famille des triterpéniques cycliques et des esters de l'acide-hydroxybenzoïque, respectivement. Ils sont… (more)

Subjects/Keywords: Cucurbitacines; Parabènes; Glucuronoconjugaison; Hydrolyse; Cytotoxicité; Chondrosarcome; Cucurbitacins; Parabens; Glucuronidation; Hydrolysis; Cytotoxicity; Chondrosarcoma; 572.567; 616.994

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APA (6th Edition):

Abbas, S. (2012). Étude des propriétés de deux séries de substances d'origine naturelle : les cucurbitacines et les parabènes : analyse de leur biotransformation chez l'homme et mesure du pouvoir cytotoxique des cucurbitacines sur une lignée cellulaire de chondrosarcome humain : Study of the properties of two series of natural derived substances : the cucurbitacins and the parabens : analysis of their biotransformation in man and measure of cucurbitacins cytotoxicity on a human chondrosarcoma cell line. (Doctoral Dissertation). Université de Lorraine. Retrieved from http://www.theses.fr/2012LORR0135

Chicago Manual of Style (16th Edition):

Abbas, Suzanne. “Étude des propriétés de deux séries de substances d'origine naturelle : les cucurbitacines et les parabènes : analyse de leur biotransformation chez l'homme et mesure du pouvoir cytotoxique des cucurbitacines sur une lignée cellulaire de chondrosarcome humain : Study of the properties of two series of natural derived substances : the cucurbitacins and the parabens : analysis of their biotransformation in man and measure of cucurbitacins cytotoxicity on a human chondrosarcoma cell line.” 2012. Doctoral Dissertation, Université de Lorraine. Accessed May 25, 2019. http://www.theses.fr/2012LORR0135.

MLA Handbook (7th Edition):

Abbas, Suzanne. “Étude des propriétés de deux séries de substances d'origine naturelle : les cucurbitacines et les parabènes : analyse de leur biotransformation chez l'homme et mesure du pouvoir cytotoxique des cucurbitacines sur une lignée cellulaire de chondrosarcome humain : Study of the properties of two series of natural derived substances : the cucurbitacins and the parabens : analysis of their biotransformation in man and measure of cucurbitacins cytotoxicity on a human chondrosarcoma cell line.” 2012. Web. 25 May 2019.

Vancouver:

Abbas S. Étude des propriétés de deux séries de substances d'origine naturelle : les cucurbitacines et les parabènes : analyse de leur biotransformation chez l'homme et mesure du pouvoir cytotoxique des cucurbitacines sur une lignée cellulaire de chondrosarcome humain : Study of the properties of two series of natural derived substances : the cucurbitacins and the parabens : analysis of their biotransformation in man and measure of cucurbitacins cytotoxicity on a human chondrosarcoma cell line. [Internet] [Doctoral dissertation]. Université de Lorraine; 2012. [cited 2019 May 25]. Available from: http://www.theses.fr/2012LORR0135.

Council of Science Editors:

Abbas S. Étude des propriétés de deux séries de substances d'origine naturelle : les cucurbitacines et les parabènes : analyse de leur biotransformation chez l'homme et mesure du pouvoir cytotoxique des cucurbitacines sur une lignée cellulaire de chondrosarcome humain : Study of the properties of two series of natural derived substances : the cucurbitacins and the parabens : analysis of their biotransformation in man and measure of cucurbitacins cytotoxicity on a human chondrosarcoma cell line. [Doctoral Dissertation]. Université de Lorraine; 2012. Available from: http://www.theses.fr/2012LORR0135


NSYSU

8. Cheng, Kai-Wen. Development of Bacterial Beta-glucuronidase-specific Inhibitors to Reduce Chemo-induced Intestinal Toxicity and Prevent Tumorigenesis.

Degree: PhD, Institute Of Biomedical Sciences, 2018, NSYSU

 Hepatic glucuronidation is a major route for detoxification. Drugs and carcinogens are conjugated with glucuronic acid to be inactive. However, the inactive glucuronides are reactivated… (more)

Subjects/Keywords: chemotherapy-induced diarrhea; colorectal cancer; chemoprevention; inhibitor; hepatic glucuronidation; bacterial β-glucuronidase

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APA (6th Edition):

Cheng, K. (2018). Development of Bacterial Beta-glucuronidase-specific Inhibitors to Reduce Chemo-induced Intestinal Toxicity and Prevent Tumorigenesis. (Doctoral Dissertation). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0623118-164715

Chicago Manual of Style (16th Edition):

Cheng, Kai-Wen. “Development of Bacterial Beta-glucuronidase-specific Inhibitors to Reduce Chemo-induced Intestinal Toxicity and Prevent Tumorigenesis.” 2018. Doctoral Dissertation, NSYSU. Accessed May 25, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0623118-164715.

MLA Handbook (7th Edition):

Cheng, Kai-Wen. “Development of Bacterial Beta-glucuronidase-specific Inhibitors to Reduce Chemo-induced Intestinal Toxicity and Prevent Tumorigenesis.” 2018. Web. 25 May 2019.

Vancouver:

Cheng K. Development of Bacterial Beta-glucuronidase-specific Inhibitors to Reduce Chemo-induced Intestinal Toxicity and Prevent Tumorigenesis. [Internet] [Doctoral dissertation]. NSYSU; 2018. [cited 2019 May 25]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0623118-164715.

Council of Science Editors:

Cheng K. Development of Bacterial Beta-glucuronidase-specific Inhibitors to Reduce Chemo-induced Intestinal Toxicity and Prevent Tumorigenesis. [Doctoral Dissertation]. NSYSU; 2018. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0623118-164715


University of Minnesota

9. Berg, Jeannette Zinggeler. Metabolism of nicotine and the tobacco carcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK): genetic and phenotypic variation.

Degree: PhD, Biochemistry, Molecular Bio, and Biophysics, 2009, University of Minnesota

 Nicotine is the addictive agent in tobacco and differences in nicotine metabolism may affect tobacco use, and consequently exposure to tobacco carcinogens. A lung procarcinogen… (more)

Subjects/Keywords: Cytochrome P450; Glucuronidation; Nicotine; NNK; Tobacco; UGT2B10; Biochemistry, Molecular Bio, and Biophysics

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APA (6th Edition):

Berg, J. Z. (2009). Metabolism of nicotine and the tobacco carcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK): genetic and phenotypic variation. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/57438

Chicago Manual of Style (16th Edition):

Berg, Jeannette Zinggeler. “Metabolism of nicotine and the tobacco carcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK): genetic and phenotypic variation.” 2009. Doctoral Dissertation, University of Minnesota. Accessed May 25, 2019. http://purl.umn.edu/57438.

MLA Handbook (7th Edition):

Berg, Jeannette Zinggeler. “Metabolism of nicotine and the tobacco carcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK): genetic and phenotypic variation.” 2009. Web. 25 May 2019.

Vancouver:

Berg JZ. Metabolism of nicotine and the tobacco carcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK): genetic and phenotypic variation. [Internet] [Doctoral dissertation]. University of Minnesota; 2009. [cited 2019 May 25]. Available from: http://purl.umn.edu/57438.

Council of Science Editors:

Berg JZ. Metabolism of nicotine and the tobacco carcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK): genetic and phenotypic variation. [Doctoral Dissertation]. University of Minnesota; 2009. Available from: http://purl.umn.edu/57438


University of Helsinki

10. Kallionpää, Roope. Glucuronidation of estrone and 16alfa-hydroxyestrone.

Degree: Farmaceutiska fakulteten, 2014, University of Helsinki

 Estrogeenit ovat naissukupuolihormoneja, joilla on sekä perimää vaurioittavia että solujen jakautumista kiihdyttäviä vaikutuksia. Elämänaikainen estrogeenialtistus liittyy useiden syöpien kehittymiseen. Estroni on estrogeenireseptorin heikko agonisti, mutta… (more)

Subjects/Keywords: UGT; estrogen; estrone; 16α-hydroxyestrone; UDP-glucuronosyltransferase; glucuronidation; Farmaceutisk kemi; Pharmaceutical Chemistry; Farmaseuttinen kemia

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APA (6th Edition):

Kallionpää, R. (2014). Glucuronidation of estrone and 16alfa-hydroxyestrone. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/135717

Chicago Manual of Style (16th Edition):

Kallionpää, Roope. “Glucuronidation of estrone and 16alfa-hydroxyestrone.” 2014. Masters Thesis, University of Helsinki. Accessed May 25, 2019. http://hdl.handle.net/10138/135717.

MLA Handbook (7th Edition):

Kallionpää, Roope. “Glucuronidation of estrone and 16alfa-hydroxyestrone.” 2014. Web. 25 May 2019.

Vancouver:

Kallionpää R. Glucuronidation of estrone and 16alfa-hydroxyestrone. [Internet] [Masters thesis]. University of Helsinki; 2014. [cited 2019 May 25]. Available from: http://hdl.handle.net/10138/135717.

Council of Science Editors:

Kallionpää R. Glucuronidation of estrone and 16alfa-hydroxyestrone. [Masters Thesis]. University of Helsinki; 2014. Available from: http://hdl.handle.net/10138/135717

11. Lin, Chaojie. The Comparison of Rat and Human Intestinal and Hepatic Glucuronidation of Enterolactone Derived from Flaxseed Lignans.

Degree: 2012, University of Saskatchewan

 The mammalian lignan, enterolactone (EL), is a gut microbe metabolite of plant lignan secoisolariciresinol diglucoside (SDG), which is most abundant in flaxseed. Numerous epidemiological, experimental… (more)

Subjects/Keywords: enterolactone; flaxseed; glucuronidation; intestine; liver; lignan

…25 Figure 2.6 Conjugative glucuronidation metabolites of ED… …28 Figure 2.7 Conjugative glucuronidation metabolites of EL… …x29; versus EL concentrations (µM) for EL glucuronidation by rat liver microsomes… …x29; and Km (C), for EL glucuronidation by rat liver microsomes (RLM, n=3… …CLint and Michaelis-Menten constants of EL glucuronidation by rat and human liver and… 

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APA (6th Edition):

Lin, C. (2012). The Comparison of Rat and Human Intestinal and Hepatic Glucuronidation of Enterolactone Derived from Flaxseed Lignans. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2012-11-777

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):

Lin, Chaojie. “The Comparison of Rat and Human Intestinal and Hepatic Glucuronidation of Enterolactone Derived from Flaxseed Lignans.” 2012. Thesis, University of Saskatchewan. Accessed May 25, 2019. http://hdl.handle.net/10388/ETD-2012-11-777.

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

MLA Handbook (7th Edition):

Lin, Chaojie. “The Comparison of Rat and Human Intestinal and Hepatic Glucuronidation of Enterolactone Derived from Flaxseed Lignans.” 2012. Web. 25 May 2019.

Vancouver:

Lin C. The Comparison of Rat and Human Intestinal and Hepatic Glucuronidation of Enterolactone Derived from Flaxseed Lignans. [Internet] [Thesis]. University of Saskatchewan; 2012. [cited 2019 May 25]. Available from: http://hdl.handle.net/10388/ETD-2012-11-777.

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

Council of Science Editors:

Lin C. The Comparison of Rat and Human Intestinal and Hepatic Glucuronidation of Enterolactone Derived from Flaxseed Lignans. [Thesis]. University of Saskatchewan; 2012. Available from: http://hdl.handle.net/10388/ETD-2012-11-777

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


Université de Montréal

12. Simard, Émilie. Effet de l'insuffisance rénale chronique sur les enzymes de phase II .

Degree: 2008, Université de Montréal

Subjects/Keywords: Acétylation; CYP450; Glucuronidation; IRC; N-acétyltransférase; NF-kB; Parathormone; Acetylation; CRF; CYP450; Glucuronidation; N-acetyltransferase; NF-kB; Parathormone

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APA (6th Edition):

Simard, . (2008). Effet de l'insuffisance rénale chronique sur les enzymes de phase II . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/8158

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):

Simard, Émilie. “Effet de l'insuffisance rénale chronique sur les enzymes de phase II .” 2008. Thesis, Université de Montréal. Accessed May 25, 2019. http://hdl.handle.net/1866/8158.

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

MLA Handbook (7th Edition):

Simard, Émilie. “Effet de l'insuffisance rénale chronique sur les enzymes de phase II .” 2008. Web. 25 May 2019.

Vancouver:

Simard . Effet de l'insuffisance rénale chronique sur les enzymes de phase II . [Internet] [Thesis]. Université de Montréal; 2008. [cited 2019 May 25]. Available from: http://hdl.handle.net/1866/8158.

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

Council of Science Editors:

Simard . Effet de l'insuffisance rénale chronique sur les enzymes de phase II . [Thesis]. Université de Montréal; 2008. Available from: http://hdl.handle.net/1866/8158

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


University of Helsinki

13. Mattila, Susanna. Glukuronidaation paikkaisomerian tutkimus johdoksenmuodostuksella hyödyntäen nestekromatografia-massaspektrometriaa.

Degree: Farmaceutiska fakulteten, 2012, University of Helsinki

The aim of the stydy was to evaluate how different chemical derivatization methods are suitable for characterization of regional isomers of different glucuronide conjugates. Glucuronidation(more)

Subjects/Keywords: glucuronidation; regional isomeria; derivatization; liquid chromatography; mass spectrometry; glukuronidaatio; paikkaisomeria; johdoksenmuodostus; nestekromatografia; massaspektrometria; Farmaceutisk kemi; Pharmaceutical Chemistry; Farmaseuttinen kemia; glucuronidation; regional isomeria; derivatization; liquid chromatography; mass spectrometry; glukuronidaatio; paikkaisomeria; johdoksenmuodostus; nestekromatografia; massaspektrometria

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APA (6th Edition):

Mattila, S. (2012). Glukuronidaation paikkaisomerian tutkimus johdoksenmuodostuksella hyödyntäen nestekromatografia-massaspektrometriaa. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/30105

Chicago Manual of Style (16th Edition):

Mattila, Susanna. “Glukuronidaation paikkaisomerian tutkimus johdoksenmuodostuksella hyödyntäen nestekromatografia-massaspektrometriaa.” 2012. Masters Thesis, University of Helsinki. Accessed May 25, 2019. http://hdl.handle.net/10138/30105.

MLA Handbook (7th Edition):

Mattila, Susanna. “Glukuronidaation paikkaisomerian tutkimus johdoksenmuodostuksella hyödyntäen nestekromatografia-massaspektrometriaa.” 2012. Web. 25 May 2019.

Vancouver:

Mattila S. Glukuronidaation paikkaisomerian tutkimus johdoksenmuodostuksella hyödyntäen nestekromatografia-massaspektrometriaa. [Internet] [Masters thesis]. University of Helsinki; 2012. [cited 2019 May 25]. Available from: http://hdl.handle.net/10138/30105.

Council of Science Editors:

Mattila S. Glukuronidaation paikkaisomerian tutkimus johdoksenmuodostuksella hyödyntäen nestekromatografia-massaspektrometriaa. [Masters Thesis]. University of Helsinki; 2012. Available from: http://hdl.handle.net/10138/30105


University of Helsinki

14. Järvinen, Erkka. Cell models for studying the interplay between conjugative metabolism and efflux transporters: Establishing UGT1A1, UGT2B7 and MRP3 transfected MDCK cell lines.

Degree: Farmaceutiska fakulteten, 2016, University of Helsinki

UDP-glucuronosyltransferases (UGTs) catalyse glucuronidation reactions between glucuronic acid and drug molecules, which contain nucleophilic groups, mostly hydroxyls, amines or carboxylic acids. Glucuronidation is the most… (more)

Subjects/Keywords: UGT1A1; UGT2B7; MRP2; MRP3; MDCK; interplay; glucuronidation; efflux transport; glukuronidisaatio; yhteispeli; efflux-kuljetus; Farmaceutisk kemi; Pharmaceutical Chemistry; Farmaseuttinen kemia; UGT1A1; UGT2B7; MRP2; MRP3; MDCK; interplay; glucuronidation; efflux transport; glukuronidisaatio; yhteispeli; efflux-kuljetus

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APA (6th Edition):

Järvinen, E. (2016). Cell models for studying the interplay between conjugative metabolism and efflux transporters: Establishing UGT1A1, UGT2B7 and MRP3 transfected MDCK cell lines. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/159428

Chicago Manual of Style (16th Edition):

Järvinen, Erkka. “Cell models for studying the interplay between conjugative metabolism and efflux transporters: Establishing UGT1A1, UGT2B7 and MRP3 transfected MDCK cell lines.” 2016. Masters Thesis, University of Helsinki. Accessed May 25, 2019. http://hdl.handle.net/10138/159428.

MLA Handbook (7th Edition):

Järvinen, Erkka. “Cell models for studying the interplay between conjugative metabolism and efflux transporters: Establishing UGT1A1, UGT2B7 and MRP3 transfected MDCK cell lines.” 2016. Web. 25 May 2019.

Vancouver:

Järvinen E. Cell models for studying the interplay between conjugative metabolism and efflux transporters: Establishing UGT1A1, UGT2B7 and MRP3 transfected MDCK cell lines. [Internet] [Masters thesis]. University of Helsinki; 2016. [cited 2019 May 25]. Available from: http://hdl.handle.net/10138/159428.

Council of Science Editors:

Järvinen E. Cell models for studying the interplay between conjugative metabolism and efflux transporters: Establishing UGT1A1, UGT2B7 and MRP3 transfected MDCK cell lines. [Masters Thesis]. University of Helsinki; 2016. Available from: http://hdl.handle.net/10138/159428


Virginia Commonwealth University

15. Thekkudan, Dennis. Multidimensional Methods: Applications in Drug-Enzyme Intrinsic Clearance Determination and Comprehensive Two-Dimensional Liquid Chromatography Peak Volume Determination.

Degree: PhD, Chemistry, 2009, Virginia Commonwealth University

 The goal of the first project was to evaluate strategies for determining the in vitro intrinsic clearance (CLint) of dextrorphan (DR) as metabolized by the… (more)

Subjects/Keywords: Drug metabolism; Dextrorphan; Glucuronidation; UGT2B7; Enzyme kinetics; Pseudo-first-order kinetics; Comprehensive two-dimensional liquid chromatography; Volume estimation; Gaussian; Nonlinear fitting algorithm; Moments; Peak Volume; Chemistry; Physical Sciences and Mathematics

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APA (6th Edition):

Thekkudan, D. (2009). Multidimensional Methods: Applications in Drug-Enzyme Intrinsic Clearance Determination and Comprehensive Two-Dimensional Liquid Chromatography Peak Volume Determination. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/2005

Chicago Manual of Style (16th Edition):

Thekkudan, Dennis. “Multidimensional Methods: Applications in Drug-Enzyme Intrinsic Clearance Determination and Comprehensive Two-Dimensional Liquid Chromatography Peak Volume Determination.” 2009. Doctoral Dissertation, Virginia Commonwealth University. Accessed May 25, 2019. https://scholarscompass.vcu.edu/etd/2005.

MLA Handbook (7th Edition):

Thekkudan, Dennis. “Multidimensional Methods: Applications in Drug-Enzyme Intrinsic Clearance Determination and Comprehensive Two-Dimensional Liquid Chromatography Peak Volume Determination.” 2009. Web. 25 May 2019.

Vancouver:

Thekkudan D. Multidimensional Methods: Applications in Drug-Enzyme Intrinsic Clearance Determination and Comprehensive Two-Dimensional Liquid Chromatography Peak Volume Determination. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2009. [cited 2019 May 25]. Available from: https://scholarscompass.vcu.edu/etd/2005.

Council of Science Editors:

Thekkudan D. Multidimensional Methods: Applications in Drug-Enzyme Intrinsic Clearance Determination and Comprehensive Two-Dimensional Liquid Chromatography Peak Volume Determination. [Doctoral Dissertation]. Virginia Commonwealth University; 2009. Available from: https://scholarscompass.vcu.edu/etd/2005


University of Cincinnati

16. Al-Zoughool, Mustafa Hussein. N-Glucuronidation of 4-Aminobiphenyl and the Risk of Urinary Bladder Cancer: Gender Differences.

Degree: PhD, Medicine : Toxicology (Environmental Health), 2005, University of Cincinnati

 The current study is aimed at investigating the role of N-glucuronidation in the organotropic differences between males and females using the bladder carcinogen, 4-aminobiphenyl (4-ABP).… (more)

Subjects/Keywords: Health Sciences, Toxicology; 4-Aminobiphenyl; Bladder cancer; Aromatic amines; N-glucuronidation; DNA-adducts

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APA (6th Edition):

Al-Zoughool, M. H. (2005). N-Glucuronidation of 4-Aminobiphenyl and the Risk of Urinary Bladder Cancer: Gender Differences. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1115852691

Chicago Manual of Style (16th Edition):

Al-Zoughool, Mustafa Hussein. “N-Glucuronidation of 4-Aminobiphenyl and the Risk of Urinary Bladder Cancer: Gender Differences.” 2005. Doctoral Dissertation, University of Cincinnati. Accessed May 25, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1115852691.

MLA Handbook (7th Edition):

Al-Zoughool, Mustafa Hussein. “N-Glucuronidation of 4-Aminobiphenyl and the Risk of Urinary Bladder Cancer: Gender Differences.” 2005. Web. 25 May 2019.

Vancouver:

Al-Zoughool MH. N-Glucuronidation of 4-Aminobiphenyl and the Risk of Urinary Bladder Cancer: Gender Differences. [Internet] [Doctoral dissertation]. University of Cincinnati; 2005. [cited 2019 May 25]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1115852691.

Council of Science Editors:

Al-Zoughool MH. N-Glucuronidation of 4-Aminobiphenyl and the Risk of Urinary Bladder Cancer: Gender Differences. [Doctoral Dissertation]. University of Cincinnati; 2005. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1115852691

17. Stephens, Brian Robert. Inflammation alters phase II metabolism of alpha-mangostin in Caco-2 cells.

Degree: MS, Human Ecology: Human Nutrition, 2012, The Ohio State University

  The absorption of xenobiotics into systemic circulation is impacted by phase II metabolism in the small and large intestine. Enterocytes are absorptive cells in… (more)

Subjects/Keywords: Biology; Nutrition; glucuronidation; inflammation; alpha-mangostin; enterocyte; phase II metabolism

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APA (6th Edition):

Stephens, B. R. (2012). Inflammation alters phase II metabolism of alpha-mangostin in Caco-2 cells. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1325026750

Chicago Manual of Style (16th Edition):

Stephens, Brian Robert. “Inflammation alters phase II metabolism of alpha-mangostin in Caco-2 cells.” 2012. Masters Thesis, The Ohio State University. Accessed May 25, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1325026750.

MLA Handbook (7th Edition):

Stephens, Brian Robert. “Inflammation alters phase II metabolism of alpha-mangostin in Caco-2 cells.” 2012. Web. 25 May 2019.

Vancouver:

Stephens BR. Inflammation alters phase II metabolism of alpha-mangostin in Caco-2 cells. [Internet] [Masters thesis]. The Ohio State University; 2012. [cited 2019 May 25]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1325026750.

Council of Science Editors:

Stephens BR. Inflammation alters phase II metabolism of alpha-mangostin in Caco-2 cells. [Masters Thesis]. The Ohio State University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1325026750

18. Wu, Baojian. Experimental and Computational Approaches to Predict Glucuronidation of Phenolics.

Degree: Pharmacological and Pharmaceutical Sciences, Department of, 2012, University of Houston

 [Purpose] UDP-glucuronosyltransferases (UGTs) catalyze the glucuronidation reaction which has been increasingly recognized as an important metabolic and detoxification pathway. Contrasting with the functional significance of… (more)

Subjects/Keywords: UGTs; Glucuronidation; In silico model; QSAR; Phenolics; Flavonoids

…of glucuronidation derived from incubation of 3,3’,4’-trihydroxyflavone (33’4’THF)… …glucuronidation of estradiol (a) and propofol (b) using recombinant UGTs and pooled… …of glucuronidation derived from incubation of 3,6,4’-trihydroxyflavone (364’THF)… …80 Figure 25. UGT1A1 activity correlation between flavonoid-4’-O-glucuronidation (… …top: 33’4’THF; bottom: 364’THF) and estradiol-3-glucuronidation in a bank of HLMs (… 

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APA (6th Edition):

Wu, B. (2012). Experimental and Computational Approaches to Predict Glucuronidation of Phenolics. (Thesis). University of Houston. Retrieved from http://hdl.handle.net/10657/ETD-UH-2012-05-269

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):

Wu, Baojian. “Experimental and Computational Approaches to Predict Glucuronidation of Phenolics.” 2012. Thesis, University of Houston. Accessed May 25, 2019. http://hdl.handle.net/10657/ETD-UH-2012-05-269.

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

MLA Handbook (7th Edition):

Wu, Baojian. “Experimental and Computational Approaches to Predict Glucuronidation of Phenolics.” 2012. Web. 25 May 2019.

Vancouver:

Wu B. Experimental and Computational Approaches to Predict Glucuronidation of Phenolics. [Internet] [Thesis]. University of Houston; 2012. [cited 2019 May 25]. Available from: http://hdl.handle.net/10657/ETD-UH-2012-05-269.

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

Council of Science Editors:

Wu B. Experimental and Computational Approaches to Predict Glucuronidation of Phenolics. [Thesis]. University of Houston; 2012. Available from: http://hdl.handle.net/10657/ETD-UH-2012-05-269

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

19. Robotham, Scott Allen. Evaluation of the regioselectivity of human UDP-glucuronosyltransferase isozymes with three common sub-classes of flavonoids via metal complexation and tandem mass spectrometry.

Degree: Chemistry, 2012, University of Texas – Austin

 Based on reactions with two flavanones, three flavonols, and five flavones the regioselectivities of twelve human UDP-glucuronosyltransferase (UGT) isozymes were elucidated. The various flavonoid glucuronides… (more)

Subjects/Keywords: Human UDP-glucuronosyltransferase; Flavonoid; Regioselectivity; Mass spectrometry; Metal complexation; Glucuronidation

…and most importantly the liver .10 This process results in glucuronidation, sulfation… …paramount. Glucuronidation of flavonoids is carried out in the body by the… …Flavonoids possessing one to multiple hydroxyl groups may undergo O-glucuronidation at various… …expanded our investigation of the selectivity of glucuronidation of the twelve most common UGT… …the glucuronidation reactions was modified from the protocol reported in Davis et al.34 Each… 

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APA (6th Edition):

Robotham, S. A. (2012). Evaluation of the regioselectivity of human UDP-glucuronosyltransferase isozymes with three common sub-classes of flavonoids via metal complexation and tandem mass spectrometry. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/19676

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):

Robotham, Scott Allen. “Evaluation of the regioselectivity of human UDP-glucuronosyltransferase isozymes with three common sub-classes of flavonoids via metal complexation and tandem mass spectrometry.” 2012. Thesis, University of Texas – Austin. Accessed May 25, 2019. http://hdl.handle.net/2152/19676.

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

MLA Handbook (7th Edition):

Robotham, Scott Allen. “Evaluation of the regioselectivity of human UDP-glucuronosyltransferase isozymes with three common sub-classes of flavonoids via metal complexation and tandem mass spectrometry.” 2012. Web. 25 May 2019.

Vancouver:

Robotham SA. Evaluation of the regioselectivity of human UDP-glucuronosyltransferase isozymes with three common sub-classes of flavonoids via metal complexation and tandem mass spectrometry. [Internet] [Thesis]. University of Texas – Austin; 2012. [cited 2019 May 25]. Available from: http://hdl.handle.net/2152/19676.

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

Council of Science Editors:

Robotham SA. Evaluation of the regioselectivity of human UDP-glucuronosyltransferase isozymes with three common sub-classes of flavonoids via metal complexation and tandem mass spectrometry. [Thesis]. University of Texas – Austin; 2012. Available from: http://hdl.handle.net/2152/19676

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

20. van Beusekom, C.D. van. Feline hepatic biotransformation and transport mechanisms.

Degree: 2015, University Utrecht

 Hepatic biotransformation and drug transport mechanisms vary significantly between species. While these processes that determine largely the kinetic behavior of drugs have been studied abundantly… (more)

Subjects/Keywords: cats; drug; biotransformation; toxicity; dogs; metabolism; liver; CYP450; glucuronidation; ABC-transporters

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APA (6th Edition):

van Beusekom, C. D. v. (2015). Feline hepatic biotransformation and transport mechanisms. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/308618 ; URN:NBN:NL:UI:10-1874-308618 ; urn:isbn:978-90-393-6265-5 ; URN:NBN:NL:UI:10-1874-308618 ; http://dspace.library.uu.nl/handle/1874/308618

Chicago Manual of Style (16th Edition):

van Beusekom, C D van. “Feline hepatic biotransformation and transport mechanisms.” 2015. Doctoral Dissertation, University Utrecht. Accessed May 25, 2019. http://dspace.library.uu.nl/handle/1874/308618 ; URN:NBN:NL:UI:10-1874-308618 ; urn:isbn:978-90-393-6265-5 ; URN:NBN:NL:UI:10-1874-308618 ; http://dspace.library.uu.nl/handle/1874/308618.

MLA Handbook (7th Edition):

van Beusekom, C D van. “Feline hepatic biotransformation and transport mechanisms.” 2015. Web. 25 May 2019.

Vancouver:

van Beusekom CDv. Feline hepatic biotransformation and transport mechanisms. [Internet] [Doctoral dissertation]. University Utrecht; 2015. [cited 2019 May 25]. Available from: http://dspace.library.uu.nl/handle/1874/308618 ; URN:NBN:NL:UI:10-1874-308618 ; urn:isbn:978-90-393-6265-5 ; URN:NBN:NL:UI:10-1874-308618 ; http://dspace.library.uu.nl/handle/1874/308618.

Council of Science Editors:

van Beusekom CDv. Feline hepatic biotransformation and transport mechanisms. [Doctoral Dissertation]. University Utrecht; 2015. Available from: http://dspace.library.uu.nl/handle/1874/308618 ; URN:NBN:NL:UI:10-1874-308618 ; urn:isbn:978-90-393-6265-5 ; URN:NBN:NL:UI:10-1874-308618 ; http://dspace.library.uu.nl/handle/1874/308618


University of Helsinki

21. Hirvisaari, Laura. Katekoliestradiolien glukuronidaatio.

Degree: Farmaceutiska fakulteten, 2012, University of Helsinki

Estradiol is a female sex hormone which is metabolized to two different catechol estradiols. 2-hydroxyestradiol (2-OHE2) is normally the major catechol estradiol metabolite but breast… (more)

Subjects/Keywords: UGT; HPLC; Catechol estradiols; glucuronidation; 2-hydroxyestradiol; 4-hydroxyestradiol; UDP-glucuronosyl transferase; separation method development; glukuronidaatio; 2-hydroksiestradioli; 4-hydroksiestradioli; UDP-glukuronosyylitransferaasi; kromatografiamenetelmä; katekoliestradioli; Farmaceutisk kemi; Pharmaceutical Chemistry; Farmaseuttinen kemia; UGT; HPLC; Catechol estradiols; glucuronidation; 2-hydroxyestradiol; 4-hydroxyestradiol; UDP-glucuronosyl transferase; separation method development; glukuronidaatio; 2-hydroksiestradioli; 4-hydroksiestradioli; UDP-glukuronosyylitransferaasi; kromatografiamenetelmä; katekoliestradioli

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APA (6th Edition):

Hirvisaari, L. (2012). Katekoliestradiolien glukuronidaatio. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/35742

Chicago Manual of Style (16th Edition):

Hirvisaari, Laura. “Katekoliestradiolien glukuronidaatio.” 2012. Masters Thesis, University of Helsinki. Accessed May 25, 2019. http://hdl.handle.net/10138/35742.

MLA Handbook (7th Edition):

Hirvisaari, Laura. “Katekoliestradiolien glukuronidaatio.” 2012. Web. 25 May 2019.

Vancouver:

Hirvisaari L. Katekoliestradiolien glukuronidaatio. [Internet] [Masters thesis]. University of Helsinki; 2012. [cited 2019 May 25]. Available from: http://hdl.handle.net/10138/35742.

Council of Science Editors:

Hirvisaari L. Katekoliestradiolien glukuronidaatio. [Masters Thesis]. University of Helsinki; 2012. Available from: http://hdl.handle.net/10138/35742

22. A. Mazzolari. IN SILICO APPROACHES IN DRUG DESIGN AND DEVELOPMENT: APPLICATIONS TO RATIONAL LIGAND DESIGN AND METABOLISM PREDICTION.

Degree: 2015, Università degli Studi di Milano

 In the last decades, the applications of computational methods in medicinal chemistry have experienced significant changes which have incredibly expanded their approaches, and more importantly… (more)

Subjects/Keywords: Metabolism; ADME; UGT; UGT2B7; glucuronidation; Proteochemometric Modelling; PCM; Machine Learning; Random Forest; Modelling; MD simulations; Steered Molecular Dynamics; SMD; UDPGA; QSAR; Purinergic receptors; ATP; PELE; SPILLO-PBSS; allosteric modulators; binding site; pockets; Muscarinic receptors; conformational chimeras; 1,4-dioxane agonist; Settore CHIM/08 - Chimica Farmaceutica

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APA (6th Edition):

Mazzolari, A. (2015). IN SILICO APPROACHES IN DRUG DESIGN AND DEVELOPMENT: APPLICATIONS TO RATIONAL LIGAND DESIGN AND METABOLISM PREDICTION. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/347523

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):

Mazzolari, A.. “IN SILICO APPROACHES IN DRUG DESIGN AND DEVELOPMENT: APPLICATIONS TO RATIONAL LIGAND DESIGN AND METABOLISM PREDICTION.” 2015. Thesis, Università degli Studi di Milano. Accessed May 25, 2019. http://hdl.handle.net/2434/347523.

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

MLA Handbook (7th Edition):

Mazzolari, A.. “IN SILICO APPROACHES IN DRUG DESIGN AND DEVELOPMENT: APPLICATIONS TO RATIONAL LIGAND DESIGN AND METABOLISM PREDICTION.” 2015. Web. 25 May 2019.

Vancouver:

Mazzolari A. IN SILICO APPROACHES IN DRUG DESIGN AND DEVELOPMENT: APPLICATIONS TO RATIONAL LIGAND DESIGN AND METABOLISM PREDICTION. [Internet] [Thesis]. Università degli Studi di Milano; 2015. [cited 2019 May 25]. Available from: http://hdl.handle.net/2434/347523.

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

Council of Science Editors:

Mazzolari A. IN SILICO APPROACHES IN DRUG DESIGN AND DEVELOPMENT: APPLICATIONS TO RATIONAL LIGAND DESIGN AND METABOLISM PREDICTION. [Thesis]. Università degli Studi di Milano; 2015. Available from: http://hdl.handle.net/2434/347523

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


Universidad de Extremadura

23. Gallego Aguilera, Alicia. Variabilidad interétnica de los polimorfismos genéticos de "UGT1A4" y "CYP2C9 IVS8-109 A>T" en las poblaciones española e iberoamericanas.

Degree: 2018, Universidad de Extremadura

Subjects/Keywords: UGT1A4; CYP2C9 IVS8-109 A>; T; Españoles; Diferencias interétnicas; Interethnic differences; Glucuronidación; Glucuronidation; Polimorfismos intrónicos; Intronic polymorphisms; 3208.09 Procesos Metabólicos de Los Medicamentos; 3201.02 Genética Clínica

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APA (6th Edition):

Gallego Aguilera, A. (2018). Variabilidad interétnica de los polimorfismos genéticos de "UGT1A4" y "CYP2C9 IVS8-109 A>T" en las poblaciones española e iberoamericanas. (Thesis). Universidad de Extremadura. Retrieved from http://hdl.handle.net/10662/2844

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):

Gallego Aguilera, Alicia. “Variabilidad interétnica de los polimorfismos genéticos de "UGT1A4" y "CYP2C9 IVS8-109 A>T" en las poblaciones española e iberoamericanas.” 2018. Thesis, Universidad de Extremadura. Accessed May 25, 2019. http://hdl.handle.net/10662/2844.

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

MLA Handbook (7th Edition):

Gallego Aguilera, Alicia. “Variabilidad interétnica de los polimorfismos genéticos de "UGT1A4" y "CYP2C9 IVS8-109 A>T" en las poblaciones española e iberoamericanas.” 2018. Web. 25 May 2019.

Vancouver:

Gallego Aguilera A. Variabilidad interétnica de los polimorfismos genéticos de "UGT1A4" y "CYP2C9 IVS8-109 A>T" en las poblaciones española e iberoamericanas. [Internet] [Thesis]. Universidad de Extremadura; 2018. [cited 2019 May 25]. Available from: http://hdl.handle.net/10662/2844.

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

Council of Science Editors:

Gallego Aguilera A. Variabilidad interétnica de los polimorfismos genéticos de "UGT1A4" y "CYP2C9 IVS8-109 A>T" en las poblaciones española e iberoamericanas. [Thesis]. Universidad de Extremadura; 2018. Available from: http://hdl.handle.net/10662/2844

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

24. 鈴木, 利一. 新規強心剤Denopamineの代謝に関する研究 : Metabolism of Denopamine, a new cardiotonic agent.

Degree: Chiba University / 千葉大学

研究科: 千葉大学大学院薬学研究院

学位:千大院薬博乙第29号

Advisors/Committee Members: 千葉大学大学院薬学研究院.

Subjects/Keywords: metabolism; oxidation; GC/MS; glucuronidation; denopamine; cardiotonic agent; microsome; 代謝; 酸化; ガスクロマトグラフィ; 質量分析; グルクロン酸化; デノパミン; 強化剤; ミクロゾーム

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APA (6th Edition):

鈴木, . (n.d.). 新規強心剤Denopamineの代謝に関する研究 : Metabolism of Denopamine, a new cardiotonic agent. (Thesis). Chiba University / 千葉大学. Retrieved from http://opac.ll.chiba-u.jp/da/curator/900022744/

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

鈴木, 利一. “新規強心剤Denopamineの代謝に関する研究 : Metabolism of Denopamine, a new cardiotonic agent.” Thesis, Chiba University / 千葉大学. Accessed May 25, 2019. http://opac.ll.chiba-u.jp/da/curator/900022744/.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

鈴木, 利一. “新規強心剤Denopamineの代謝に関する研究 : Metabolism of Denopamine, a new cardiotonic agent.” Web. 25 May 2019.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

鈴木 . 新規強心剤Denopamineの代謝に関する研究 : Metabolism of Denopamine, a new cardiotonic agent. [Internet] [Thesis]. Chiba University / 千葉大学; [cited 2019 May 25]. Available from: http://opac.ll.chiba-u.jp/da/curator/900022744/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

鈴木 . 新規強心剤Denopamineの代謝に関する研究 : Metabolism of Denopamine, a new cardiotonic agent. [Thesis]. Chiba University / 千葉大学; Available from: http://opac.ll.chiba-u.jp/da/curator/900022744/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


University of Florida

25. Mohamed, Mohamed. Characterization of Herb-Drug Interactions through Glucuronidation.

Degree: PhD, Pharmaceutical Sciences - Pharmaceutics, 2010, University of Florida

 The use of herbal supplements has continued to increase over the last decade. Many herbal supplement users concomitantly take prescription and non-prescription drugs, raising the… (more)

Subjects/Keywords: Dosage; Drug interactions; Enzymes; Green teas; Herb drug interactions; In vitro fertilization; Incubation; Inhibitory concentration 50; Metabolism; Milk; cohosh, cranberry, echinacea, egcg, garlic, ginkgo, ginseng, glucuronidation, herb, incubation, inhibition, interactions, intestine, liver, metabolism, microsomes, mpa, palmetto, pharmacokinetics, phytochemicals, raloxifene, saw, tea, thistle, ugt, ugt1a, ugt1a1, ugt1a4, ugt1a6, ugt1a9, valerian

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APA (6th Edition):

Mohamed, M. (2010). Characterization of Herb-Drug Interactions through Glucuronidation. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0041440

Chicago Manual of Style (16th Edition):

Mohamed, Mohamed. “Characterization of Herb-Drug Interactions through Glucuronidation.” 2010. Doctoral Dissertation, University of Florida. Accessed May 25, 2019. http://ufdc.ufl.edu/UFE0041440.

MLA Handbook (7th Edition):

Mohamed, Mohamed. “Characterization of Herb-Drug Interactions through Glucuronidation.” 2010. Web. 25 May 2019.

Vancouver:

Mohamed M. Characterization of Herb-Drug Interactions through Glucuronidation. [Internet] [Doctoral dissertation]. University of Florida; 2010. [cited 2019 May 25]. Available from: http://ufdc.ufl.edu/UFE0041440.

Council of Science Editors:

Mohamed M. Characterization of Herb-Drug Interactions through Glucuronidation. [Doctoral Dissertation]. University of Florida; 2010. Available from: http://ufdc.ufl.edu/UFE0041440

26. Le Clair, Michael W. Distribution and Elimination of 3-Trifluoromethyl-4-Nitrophenol (TFM) by Sea Lamprey (Petromyzon marinus) and Non-target, Rainbow Trout (Oncorhynchus mykiss) and Lake Sturgeon (Acipenser fulvescens).

Degree: 2014, Wilfrid Laurier University

 The pesticide, 3-trifluoromethyl-4-nitrophenol (TFM), has been highly successful in the control of sea lamprey (Petromyzon marinus) populations in the Great Lakes. Treatments with TFM involve… (more)

Subjects/Keywords: glucuronidation; glucuronide; metabolite; Aquaculture and Fisheries; Biochemistry; Biology; Comparative and Evolutionary Physiology; Marine Biology; Other Animal Sciences; Toxicology

…15 Figure 1-5: Process of glucuronidation ..........................17… …inability of larval sea lamprey to detoxify TFM via glucuronidation leads to greater build-up of… …TFM, and greater toxicity (Lech et al., 1974). Glucuronidation takes 5 place in… …knowledge of TFM glucuronidation could help better determine why TFM is selective to lamprey… …findings is that sea lampreys may increase their capacity to detoxify TFM via glucuronidation… 

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APA (6th Edition):

Le Clair, M. W. (2014). Distribution and Elimination of 3-Trifluoromethyl-4-Nitrophenol (TFM) by Sea Lamprey (Petromyzon marinus) and Non-target, Rainbow Trout (Oncorhynchus mykiss) and Lake Sturgeon (Acipenser fulvescens). (Thesis). Wilfrid Laurier University. Retrieved from https://scholars.wlu.ca/etd/1632

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):

Le Clair, Michael W. “Distribution and Elimination of 3-Trifluoromethyl-4-Nitrophenol (TFM) by Sea Lamprey (Petromyzon marinus) and Non-target, Rainbow Trout (Oncorhynchus mykiss) and Lake Sturgeon (Acipenser fulvescens).” 2014. Thesis, Wilfrid Laurier University. Accessed May 25, 2019. https://scholars.wlu.ca/etd/1632.

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

MLA Handbook (7th Edition):

Le Clair, Michael W. “Distribution and Elimination of 3-Trifluoromethyl-4-Nitrophenol (TFM) by Sea Lamprey (Petromyzon marinus) and Non-target, Rainbow Trout (Oncorhynchus mykiss) and Lake Sturgeon (Acipenser fulvescens).” 2014. Web. 25 May 2019.

Vancouver:

Le Clair MW. Distribution and Elimination of 3-Trifluoromethyl-4-Nitrophenol (TFM) by Sea Lamprey (Petromyzon marinus) and Non-target, Rainbow Trout (Oncorhynchus mykiss) and Lake Sturgeon (Acipenser fulvescens). [Internet] [Thesis]. Wilfrid Laurier University; 2014. [cited 2019 May 25]. Available from: https://scholars.wlu.ca/etd/1632.

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

Council of Science Editors:

Le Clair MW. Distribution and Elimination of 3-Trifluoromethyl-4-Nitrophenol (TFM) by Sea Lamprey (Petromyzon marinus) and Non-target, Rainbow Trout (Oncorhynchus mykiss) and Lake Sturgeon (Acipenser fulvescens). [Thesis]. Wilfrid Laurier University; 2014. Available from: https://scholars.wlu.ca/etd/1632

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

27. Jackson, Erin N. Interaction of Triclosan with Human and Sheep Phase II Enzymes.

Degree: PhD, Pharmaceutical Sciences - Medicinal Chemistry, 2015, University of Florida

 Triclosan, a widely used antibacterial, is now prevalent in the environment and has been detected in various human tissues. Unrelated to its mode of antibacterial… (more)

Subjects/Keywords: Enzymes; Estrogens; Liver; Metabolism; Placenta; Protein isoforms; Sheep; Steroids; Sulfates; Women; glucuronidation  – inhibition  – metabolism  – pregnancy  – sulfonation  – triclosan

…68 2-1 Triclosan glucuronidation by individual UGT isoforms… …87 2-2 Kinetics of triclosan glucuronidation by the human UGT isoforms with highest… …87 2-3 Triclosan glucuronidation activity (nmol/min/mg protein) and UGT… …91 2-5 UGT1A1 expression does not predict triclosan glucuronidation activity… …glucuronidation activity… 

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APA (6th Edition):

Jackson, E. N. (2015). Interaction of Triclosan with Human and Sheep Phase II Enzymes. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0048994

Chicago Manual of Style (16th Edition):

Jackson, Erin N. “Interaction of Triclosan with Human and Sheep Phase II Enzymes.” 2015. Doctoral Dissertation, University of Florida. Accessed May 25, 2019. http://ufdc.ufl.edu/UFE0048994.

MLA Handbook (7th Edition):

Jackson, Erin N. “Interaction of Triclosan with Human and Sheep Phase II Enzymes.” 2015. Web. 25 May 2019.

Vancouver:

Jackson EN. Interaction of Triclosan with Human and Sheep Phase II Enzymes. [Internet] [Doctoral dissertation]. University of Florida; 2015. [cited 2019 May 25]. Available from: http://ufdc.ufl.edu/UFE0048994.

Council of Science Editors:

Jackson EN. Interaction of Triclosan with Human and Sheep Phase II Enzymes. [Doctoral Dissertation]. University of Florida; 2015. Available from: http://ufdc.ufl.edu/UFE0048994

28. Singh, Rashim. Relationship Between Flavonoid Structure And Phase-II Metabolism.

Degree: Pharmacological and Pharmaceutical Sciences, Department of, 2010, University of Houston

 Objective: The overall objective is to develop structure-metabolism relationships (SMRs) between UGTs and flavonoids for predicting glucuronidation of flavonoids. The goals of this research project… (more)

Subjects/Keywords: Flavonoid; Disposition of Flavonoid in Caco-2 Cells via Glucuronidation and Sulfation; Structure-metabolism relationship; Structure-metabolism relationship between Flavonoid and UGT isoforms

…50 3.1.2. Solubility and stability of the flavonoids in glucuronidation reaction mixture… …51 3.2. Glucuronidation Experiment… …60 3.7. Statistical Analysis for Glucuronidation and Caco-2 Cell Experiments Data… …GLUCURONIDATION OF FLAVONOIDS IN HUMANS… …68 4.3.3. Glucuronidation activities of recombinant human UGTs… 

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

APA (6th Edition):

Singh, R. (2010). Relationship Between Flavonoid Structure And Phase-II Metabolism. (Thesis). University of Houston. Retrieved from http://hdl.handle.net/10657/ETD-UH-2010-05-33

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):

Singh, Rashim. “Relationship Between Flavonoid Structure And Phase-II Metabolism.” 2010. Thesis, University of Houston. Accessed May 25, 2019. http://hdl.handle.net/10657/ETD-UH-2010-05-33.

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

MLA Handbook (7th Edition):

Singh, Rashim. “Relationship Between Flavonoid Structure And Phase-II Metabolism.” 2010. Web. 25 May 2019.

Vancouver:

Singh R. Relationship Between Flavonoid Structure And Phase-II Metabolism. [Internet] [Thesis]. University of Houston; 2010. [cited 2019 May 25]. Available from: http://hdl.handle.net/10657/ETD-UH-2010-05-33.

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

Council of Science Editors:

Singh R. Relationship Between Flavonoid Structure And Phase-II Metabolism. [Thesis]. University of Houston; 2010. Available from: http://hdl.handle.net/10657/ETD-UH-2010-05-33

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

.