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You searched for subject:(Cytochrome P450 3A4 CYP3A4 ). Showing records 1 – 30 of 1319 total matches.

[1] [2] [3] [4] [5] … [44]

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University of Utah

1. Moore, Chad Douglas. Dehydrogenation of Raloxifene by Cytochrome P450 3A4.

Degree: PhD, Pharmacology & Toxicology;, 2010, University of Utah

 Raloxifene was approved in 2007 by the FDA for the chemoprevention of breast cancer in postmenopausal women with osteoporosis and in postmenopausal women at high… (more)

Subjects/Keywords: Raloxifene; Dehydrogenation; Cytochrome P450 3A4

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

APA (6th Edition):

Moore, C. D. (2010). Dehydrogenation of Raloxifene by Cytochrome P450 3A4. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1401/rec/288

Chicago Manual of Style (16th Edition):

Moore, Chad Douglas. “Dehydrogenation of Raloxifene by Cytochrome P450 3A4.” 2010. Doctoral Dissertation, University of Utah. Accessed January 21, 2021. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1401/rec/288.

MLA Handbook (7th Edition):

Moore, Chad Douglas. “Dehydrogenation of Raloxifene by Cytochrome P450 3A4.” 2010. Web. 21 Jan 2021.

Vancouver:

Moore CD. Dehydrogenation of Raloxifene by Cytochrome P450 3A4. [Internet] [Doctoral dissertation]. University of Utah; 2010. [cited 2021 Jan 21]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1401/rec/288.

Council of Science Editors:

Moore CD. Dehydrogenation of Raloxifene by Cytochrome P450 3A4. [Doctoral Dissertation]. University of Utah; 2010. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1401/rec/288


North-West University

2. Mgwabi, Mthokozisi Muziwandile Nkosingiphile. Genetic polymorphism in dextromethorphan metabolism by CYP2D6 and CYP3A4 enzyme isoforms / Mthokozisi Muziwandile Nkosingiphile Mgwabi .

Degree: 2003, North-West University

 Most administered drugs are metabolised in the liver by Phase I enzymes and more importantly by the cytochrome P450 (CYP) system. The extent of first-pass… (more)

Subjects/Keywords: HPLC; Cytochrome P450 2D6 (CYP2D6); Cytochrome P450 3A4 (CYP3A4); Dextromethorphan; Metabolism; Phenotyping

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APA (6th Edition):

Mgwabi, M. M. N. (2003). Genetic polymorphism in dextromethorphan metabolism by CYP2D6 and CYP3A4 enzyme isoforms / Mthokozisi Muziwandile Nkosingiphile Mgwabi . (Thesis). North-West University. Retrieved from http://hdl.handle.net/10394/163

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):

Mgwabi, Mthokozisi Muziwandile Nkosingiphile. “Genetic polymorphism in dextromethorphan metabolism by CYP2D6 and CYP3A4 enzyme isoforms / Mthokozisi Muziwandile Nkosingiphile Mgwabi .” 2003. Thesis, North-West University. Accessed January 21, 2021. http://hdl.handle.net/10394/163.

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

MLA Handbook (7th Edition):

Mgwabi, Mthokozisi Muziwandile Nkosingiphile. “Genetic polymorphism in dextromethorphan metabolism by CYP2D6 and CYP3A4 enzyme isoforms / Mthokozisi Muziwandile Nkosingiphile Mgwabi .” 2003. Web. 21 Jan 2021.

Vancouver:

Mgwabi MMN. Genetic polymorphism in dextromethorphan metabolism by CYP2D6 and CYP3A4 enzyme isoforms / Mthokozisi Muziwandile Nkosingiphile Mgwabi . [Internet] [Thesis]. North-West University; 2003. [cited 2021 Jan 21]. Available from: http://hdl.handle.net/10394/163.

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

Council of Science Editors:

Mgwabi MMN. Genetic polymorphism in dextromethorphan metabolism by CYP2D6 and CYP3A4 enzyme isoforms / Mthokozisi Muziwandile Nkosingiphile Mgwabi . [Thesis]. North-West University; 2003. Available from: http://hdl.handle.net/10394/163

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


University of Illinois – Urbana-Champaign

3. Frank, Daniel J. Global deconvolution of heterotropic cooperativity in cytochrome P450 3A4.

Degree: PhD, 0318, 2011, University of Illinois – Urbana-Champaign

Cytochrome P450 3A4 (CYP3A4) plays a central role in xenobiotic metabolism, and is of critical importance to both human health and the pharmaceutical industry. Its… (more)

Subjects/Keywords: cooperativity; cytochrome P450 3A4; drug-drug interactions

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APA (6th Edition):

Frank, D. J. (2011). Global deconvolution of heterotropic cooperativity in cytochrome P450 3A4. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/24520

Chicago Manual of Style (16th Edition):

Frank, Daniel J. “Global deconvolution of heterotropic cooperativity in cytochrome P450 3A4.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed January 21, 2021. http://hdl.handle.net/2142/24520.

MLA Handbook (7th Edition):

Frank, Daniel J. “Global deconvolution of heterotropic cooperativity in cytochrome P450 3A4.” 2011. Web. 21 Jan 2021.

Vancouver:

Frank DJ. Global deconvolution of heterotropic cooperativity in cytochrome P450 3A4. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2021 Jan 21]. Available from: http://hdl.handle.net/2142/24520.

Council of Science Editors:

Frank DJ. Global deconvolution of heterotropic cooperativity in cytochrome P450 3A4. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/24520


University of the Western Cape

4. Feleni, Usisipho. Palladium telluride quantum dots biosensor for the determination of indinavir drug .

Degree: 2013, University of the Western Cape

 Indinavir is a potent and well tolerated protease inhibitor drug used as a component of the highly active antiretroviral therapy (HAART) of HIV/AIDS, which results… (more)

Subjects/Keywords: Indinavir drug; Cytochrome P450-3A4 (CYP3A4); Quantum dots; Self-assembled monolayers; Biosensors; Cyclic voltammetry; Limit of detection (LOD); Therapeutic drug monitoring (TDM)

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APA (6th Edition):

Feleni, U. (2013). Palladium telluride quantum dots biosensor for the determination of indinavir drug . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/3504

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):

Feleni, Usisipho. “Palladium telluride quantum dots biosensor for the determination of indinavir drug .” 2013. Thesis, University of the Western Cape. Accessed January 21, 2021. http://hdl.handle.net/11394/3504.

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

MLA Handbook (7th Edition):

Feleni, Usisipho. “Palladium telluride quantum dots biosensor for the determination of indinavir drug .” 2013. Web. 21 Jan 2021.

Vancouver:

Feleni U. Palladium telluride quantum dots biosensor for the determination of indinavir drug . [Internet] [Thesis]. University of the Western Cape; 2013. [cited 2021 Jan 21]. Available from: http://hdl.handle.net/11394/3504.

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

Council of Science Editors:

Feleni U. Palladium telluride quantum dots biosensor for the determination of indinavir drug . [Thesis]. University of the Western Cape; 2013. Available from: http://hdl.handle.net/11394/3504

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


University of Illinois – Chicago

5. Zhang, Shu. Transcriptional Regulation of CYP3A4 and CYP2D6 by Small Heterodimer Partner.

Degree: 2016, University of Illinois – Chicago

 Small heterodimer partner (SHP) is a transcriptional corepressor of a number of ligand regulated nuclear receptors (NR) and orphan receptors, and represses their target genes… (more)

Subjects/Keywords: Cytochrome P450; CYP3A4; CYP2D6; FXR; ATRA

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APA (6th Edition):

Zhang, S. (2016). Transcriptional Regulation of CYP3A4 and CYP2D6 by Small Heterodimer Partner. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/21572

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):

Zhang, Shu. “Transcriptional Regulation of CYP3A4 and CYP2D6 by Small Heterodimer Partner.” 2016. Thesis, University of Illinois – Chicago. Accessed January 21, 2021. http://hdl.handle.net/10027/21572.

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

MLA Handbook (7th Edition):

Zhang, Shu. “Transcriptional Regulation of CYP3A4 and CYP2D6 by Small Heterodimer Partner.” 2016. Web. 21 Jan 2021.

Vancouver:

Zhang S. Transcriptional Regulation of CYP3A4 and CYP2D6 by Small Heterodimer Partner. [Internet] [Thesis]. University of Illinois – Chicago; 2016. [cited 2021 Jan 21]. Available from: http://hdl.handle.net/10027/21572.

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

Council of Science Editors:

Zhang S. Transcriptional Regulation of CYP3A4 and CYP2D6 by Small Heterodimer Partner. [Thesis]. University of Illinois – Chicago; 2016. Available from: http://hdl.handle.net/10027/21572

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


University of Illinois – Chicago

6. Zhang, Shu. Transcriptional Regulation of CYP3A4 and CYP2D6 by Small Heterodimer Partner.

Degree: 2016, University of Illinois – Chicago

 Small heterodimer partner (SHP) is a transcriptional corepressor of a number of ligand regulated nuclear receptors (NR) and orphan receptors, and represses their target genes… (more)

Subjects/Keywords: Cytochrome P450; CYP3A4; CYP2D6; FXR; ATRA

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APA (6th Edition):

Zhang, S. (2016). Transcriptional Regulation of CYP3A4 and CYP2D6 by Small Heterodimer Partner. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/21629

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):

Zhang, Shu. “Transcriptional Regulation of CYP3A4 and CYP2D6 by Small Heterodimer Partner.” 2016. Thesis, University of Illinois – Chicago. Accessed January 21, 2021. http://hdl.handle.net/10027/21629.

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

MLA Handbook (7th Edition):

Zhang, Shu. “Transcriptional Regulation of CYP3A4 and CYP2D6 by Small Heterodimer Partner.” 2016. Web. 21 Jan 2021.

Vancouver:

Zhang S. Transcriptional Regulation of CYP3A4 and CYP2D6 by Small Heterodimer Partner. [Internet] [Thesis]. University of Illinois – Chicago; 2016. [cited 2021 Jan 21]. Available from: http://hdl.handle.net/10027/21629.

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

Council of Science Editors:

Zhang S. Transcriptional Regulation of CYP3A4 and CYP2D6 by Small Heterodimer Partner. [Thesis]. University of Illinois – Chicago; 2016. Available from: http://hdl.handle.net/10027/21629

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


University of Illinois – Chicago

7. Zhang, Shu. Transcriptional Regulation of CYP3A4 and CYP2D6 by Small Heterodimer Partner.

Degree: 2016, University of Illinois – Chicago

 Small heterodimer partner (SHP) is a transcriptional corepressor of a number of ligand regulated nuclear receptors (NR) and orphan receptors, and represses their target genes… (more)

Subjects/Keywords: Cytochrome P450; CYP3A4; CYP2D6; FXR; ATRA

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Zhang, S. (2016). Transcriptional Regulation of CYP3A4 and CYP2D6 by Small Heterodimer Partner. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/21630

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):

Zhang, Shu. “Transcriptional Regulation of CYP3A4 and CYP2D6 by Small Heterodimer Partner.” 2016. Thesis, University of Illinois – Chicago. Accessed January 21, 2021. http://hdl.handle.net/10027/21630.

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

MLA Handbook (7th Edition):

Zhang, Shu. “Transcriptional Regulation of CYP3A4 and CYP2D6 by Small Heterodimer Partner.” 2016. Web. 21 Jan 2021.

Vancouver:

Zhang S. Transcriptional Regulation of CYP3A4 and CYP2D6 by Small Heterodimer Partner. [Internet] [Thesis]. University of Illinois – Chicago; 2016. [cited 2021 Jan 21]. Available from: http://hdl.handle.net/10027/21630.

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

Council of Science Editors:

Zhang S. Transcriptional Regulation of CYP3A4 and CYP2D6 by Small Heterodimer Partner. [Thesis]. University of Illinois – Chicago; 2016. Available from: http://hdl.handle.net/10027/21630

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

8. Benkaidali, Lydia. Etude et applications de nouveaux modèles géométriques des canaux d'accès au site actif de certains cytochromes P450 humains par des ligands volumineux : Analysis and applications of new geometrical models of active site access channels of some human cytochromes P450 for large ligands.

Degree: Docteur es, Chimie Théorique, 2016, Université Pierre et Marie Curie – Paris VI

Les cytochromes P450s (CYPs) sont des hémoprotéines intervenant dans la fonction de détoxication cellulaire. Le site actif des CYPs est enfoui dans la protéine, mais… (more)

Subjects/Keywords: Cytochrome P450; CYP 3A4; Site actif; Cavité; Canal; Triangulation de Delaunay; Channel; CYP 3A4; Cytochrome P450; 541.2

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APA (6th Edition):

Benkaidali, L. (2016). Etude et applications de nouveaux modèles géométriques des canaux d'accès au site actif de certains cytochromes P450 humains par des ligands volumineux : Analysis and applications of new geometrical models of active site access channels of some human cytochromes P450 for large ligands. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2016PA066377

Chicago Manual of Style (16th Edition):

Benkaidali, Lydia. “Etude et applications de nouveaux modèles géométriques des canaux d'accès au site actif de certains cytochromes P450 humains par des ligands volumineux : Analysis and applications of new geometrical models of active site access channels of some human cytochromes P450 for large ligands.” 2016. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed January 21, 2021. http://www.theses.fr/2016PA066377.

MLA Handbook (7th Edition):

Benkaidali, Lydia. “Etude et applications de nouveaux modèles géométriques des canaux d'accès au site actif de certains cytochromes P450 humains par des ligands volumineux : Analysis and applications of new geometrical models of active site access channels of some human cytochromes P450 for large ligands.” 2016. Web. 21 Jan 2021.

Vancouver:

Benkaidali L. Etude et applications de nouveaux modèles géométriques des canaux d'accès au site actif de certains cytochromes P450 humains par des ligands volumineux : Analysis and applications of new geometrical models of active site access channels of some human cytochromes P450 for large ligands. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. [cited 2021 Jan 21]. Available from: http://www.theses.fr/2016PA066377.

Council of Science Editors:

Benkaidali L. Etude et applications de nouveaux modèles géométriques des canaux d'accès au site actif de certains cytochromes P450 humains par des ligands volumineux : Analysis and applications of new geometrical models of active site access channels of some human cytochromes P450 for large ligands. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. Available from: http://www.theses.fr/2016PA066377


RMIT University

9. 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 January 21, 2021. 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. 21 Jan 2021.

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 2021 Jan 21]. 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


Vilnius University

10. Dapkūnas, Justas. Citochromų P450 katalizuojamo vaistų metabolizmo kompiuterinis modeliavimas.

Degree: PhD, Biochemistry, 2011, Vilnius University

Pagrindinis šio darbo tikslas buvo kiekybinio struktūros ir aktyvumo ryšio modelių, prognozuojančių su vaistų metabolizmu susijusias savybes, kūrimas. Modeliai, prognozuojantys CYP3A4 slopinimą ir žmogaus kepenų… (more)

Subjects/Keywords: Citochromai P450; QSAR; CYP3A4 slopinimas; Vaistų metabolizmas; Regioselektyvumo progozavimas; Cytochrome P450; QSAR; CYP3A4 inhibition; Drug metabolism; Regioselectivity prediction

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APA (6th Edition):

Dapkūnas, J. (2011). Citochromų P450 katalizuojamo vaistų metabolizmo kompiuterinis modeliavimas. (Doctoral Dissertation). Vilnius University. Retrieved from http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2011~D_20111003_114342-83717 ;

Chicago Manual of Style (16th Edition):

Dapkūnas, Justas. “Citochromų P450 katalizuojamo vaistų metabolizmo kompiuterinis modeliavimas.” 2011. Doctoral Dissertation, Vilnius University. Accessed January 21, 2021. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2011~D_20111003_114342-83717 ;.

MLA Handbook (7th Edition):

Dapkūnas, Justas. “Citochromų P450 katalizuojamo vaistų metabolizmo kompiuterinis modeliavimas.” 2011. Web. 21 Jan 2021.

Vancouver:

Dapkūnas J. Citochromų P450 katalizuojamo vaistų metabolizmo kompiuterinis modeliavimas. [Internet] [Doctoral dissertation]. Vilnius University; 2011. [cited 2021 Jan 21]. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2011~D_20111003_114342-83717 ;.

Council of Science Editors:

Dapkūnas J. Citochromų P450 katalizuojamo vaistų metabolizmo kompiuterinis modeliavimas. [Doctoral Dissertation]. Vilnius University; 2011. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2011~D_20111003_114342-83717 ;


Vilnius University

11. Dapkūnas, Justas. Computational modeling of cytochrome P450-mediated drug metabolism.

Degree: Dissertation, Biochemistry, 2011, Vilnius University

The main objective of this study was the development of QSAR models for drug metabolism-related properties. Novel GALAS (Global, Adjusted Locally According to Similarity) modeling… (more)

Subjects/Keywords: Cytochrome P450; QSAR; CYP3A4 inhibition; Drug metabolism; Regioselectivity prediction; Citochromai P450; QSAR; CYP3A4 slopinimas; Vaistų metabolizmas; Regioselektyvumo prognozavimas

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

APA (6th Edition):

Dapkūnas, J. (2011). Computational modeling of cytochrome P450-mediated drug metabolism. (Doctoral Dissertation). Vilnius University. Retrieved from http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2011~D_20111003_114651-54627 ;

Chicago Manual of Style (16th Edition):

Dapkūnas, Justas. “Computational modeling of cytochrome P450-mediated drug metabolism.” 2011. Doctoral Dissertation, Vilnius University. Accessed January 21, 2021. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2011~D_20111003_114651-54627 ;.

MLA Handbook (7th Edition):

Dapkūnas, Justas. “Computational modeling of cytochrome P450-mediated drug metabolism.” 2011. Web. 21 Jan 2021.

Vancouver:

Dapkūnas J. Computational modeling of cytochrome P450-mediated drug metabolism. [Internet] [Doctoral dissertation]. Vilnius University; 2011. [cited 2021 Jan 21]. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2011~D_20111003_114651-54627 ;.

Council of Science Editors:

Dapkūnas J. Computational modeling of cytochrome P450-mediated drug metabolism. [Doctoral Dissertation]. Vilnius University; 2011. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2011~D_20111003_114651-54627 ;


Texas A&M University

12. 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 January 21, 2021. 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. 21 Jan 2021.

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 2021 Jan 21]. 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

13. Choy, Alison Pui Ki. Prediction of metabolic stability and bioavailability with bioisosteric replacements.

Degree: PhD, 2018, University of Cambridge

 Drug development is a long and expensive process. Potential drug candidates can fail clinical trials due to numerous issues, including metabolic stability and efficacy issues,… (more)

Subjects/Keywords: 615.7; Sites of metabolism prediction; QSAR; Bioisostere; Bioavailability; Cytochrome P450 3A4; P-Glycoprotein

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APA (6th Edition):

Choy, A. P. K. (2018). Prediction of metabolic stability and bioavailability with bioisosteric replacements. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.26167 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753416

Chicago Manual of Style (16th Edition):

Choy, Alison Pui Ki. “Prediction of metabolic stability and bioavailability with bioisosteric replacements.” 2018. Doctoral Dissertation, University of Cambridge. Accessed January 21, 2021. https://doi.org/10.17863/CAM.26167 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753416.

MLA Handbook (7th Edition):

Choy, Alison Pui Ki. “Prediction of metabolic stability and bioavailability with bioisosteric replacements.” 2018. Web. 21 Jan 2021.

Vancouver:

Choy APK. Prediction of metabolic stability and bioavailability with bioisosteric replacements. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2021 Jan 21]. Available from: https://doi.org/10.17863/CAM.26167 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753416.

Council of Science Editors:

Choy APK. Prediction of metabolic stability and bioavailability with bioisosteric replacements. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://doi.org/10.17863/CAM.26167 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753416


University of Manchester

14. Liu, Kang-Cheng. Influence of lipid membrane environment on the kinetics of the cytochrome P450 reductase- cytochrome P450 3A4 enzyme system in nanodiscs.

Degree: PhD, 2017, University of Manchester

 The cytochrome P450 enzyme system is a multicomponent electron-transfer chain composed of a haem-containing monooxygenase cytochrome P450 (CYP) and one or more redox partners. Eukaryotic… (more)

Subjects/Keywords: 572; phospholipid; Enzyme; Superoxide; electron transfer; Enzymatic; Kinetics; Enzyme kinetics; lipid; Membrane protein; CYP3A4; Nanodisc; Cytochrome P450 Reductase; P450; Cytochrome P450; Endoplasmic reticulum

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APA (6th Edition):

Liu, K. (2017). Influence of lipid membrane environment on the kinetics of the cytochrome P450 reductase- cytochrome P450 3A4 enzyme system in nanodiscs. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/influence-of-lipid-membrane-environment-on-the-kinetics-of-the-cytochrome-p450-reductase-cytochrome-p450-3a4-enzyme-system-in-nanodiscs(b8ee4e84-1230-40cf-9b98-b5d6f457f54c).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.728255

Chicago Manual of Style (16th Edition):

Liu, Kang-Cheng. “Influence of lipid membrane environment on the kinetics of the cytochrome P450 reductase- cytochrome P450 3A4 enzyme system in nanodiscs.” 2017. Doctoral Dissertation, University of Manchester. Accessed January 21, 2021. https://www.research.manchester.ac.uk/portal/en/theses/influence-of-lipid-membrane-environment-on-the-kinetics-of-the-cytochrome-p450-reductase-cytochrome-p450-3a4-enzyme-system-in-nanodiscs(b8ee4e84-1230-40cf-9b98-b5d6f457f54c).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.728255.

MLA Handbook (7th Edition):

Liu, Kang-Cheng. “Influence of lipid membrane environment on the kinetics of the cytochrome P450 reductase- cytochrome P450 3A4 enzyme system in nanodiscs.” 2017. Web. 21 Jan 2021.

Vancouver:

Liu K. Influence of lipid membrane environment on the kinetics of the cytochrome P450 reductase- cytochrome P450 3A4 enzyme system in nanodiscs. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2021 Jan 21]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/influence-of-lipid-membrane-environment-on-the-kinetics-of-the-cytochrome-p450-reductase-cytochrome-p450-3a4-enzyme-system-in-nanodiscs(b8ee4e84-1230-40cf-9b98-b5d6f457f54c).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.728255.

Council of Science Editors:

Liu K. Influence of lipid membrane environment on the kinetics of the cytochrome P450 reductase- cytochrome P450 3A4 enzyme system in nanodiscs. [Doctoral Dissertation]. University of Manchester; 2017. Available from: https://www.research.manchester.ac.uk/portal/en/theses/influence-of-lipid-membrane-environment-on-the-kinetics-of-the-cytochrome-p450-reductase-cytochrome-p450-3a4-enzyme-system-in-nanodiscs(b8ee4e84-1230-40cf-9b98-b5d6f457f54c).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.728255


University of Western Ontario

15. 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 January 21, 2021. 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. 21 Jan 2021.

Vancouver:

Woolsey SJ. Cytochrome P450 3A4 Expression and Regulation in Non-Alcoholic Fatty Liver Disease. [Internet] [Thesis]. University of Western Ontario; 2015. [cited 2021 Jan 21]. 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 Texas – Austin

16. -0507-6023. A mechanistic study of how hepatic cytochrome P450 3A4 is regulated during infectious and non-infectious conditions.

Degree: PhD, Pharmaceutical Sciences, 2018, University of Texas – Austin

 It has been established that adenovirus infection alters the expression and function of hepatic cytochrome P450 3A (CYP3A) for 14 days in several animal models.… (more)

Subjects/Keywords: Drug metabolism; Cytochrome P450 3A4; Liver; Integrins: Adenovirus; Influenza A virus; Talin-1; Post-translational modifications

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APA (6th Edition):

-0507-6023. (2018). A mechanistic study of how hepatic cytochrome P450 3A4 is regulated during infectious and non-infectious conditions. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63382

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

Chicago Manual of Style (16th Edition):

-0507-6023. “A mechanistic study of how hepatic cytochrome P450 3A4 is regulated during infectious and non-infectious conditions.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed January 21, 2021. http://hdl.handle.net/2152/63382.

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

MLA Handbook (7th Edition):

-0507-6023. “A mechanistic study of how hepatic cytochrome P450 3A4 is regulated during infectious and non-infectious conditions.” 2018. Web. 21 Jan 2021.

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

Vancouver:

-0507-6023. A mechanistic study of how hepatic cytochrome P450 3A4 is regulated during infectious and non-infectious conditions. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2021 Jan 21]. Available from: http://hdl.handle.net/2152/63382.

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

Council of Science Editors:

-0507-6023. A mechanistic study of how hepatic cytochrome P450 3A4 is regulated during infectious and non-infectious conditions. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/63382

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


University of the Western Cape

17. Jijana, Abongile Nwabisa. Development of electrochemical ZnSe Quantam dots biosensors for low-level detection of 17β-Estradiol estrogenic endocrine disrupting compound .

Degree: 2010, University of the Western Cape

 The main thesis hub was on development of two electrochemical biosensors for the determination of 17β-estradiol-estradiol: an estrogenic endocrine disrupting compound. Endocronology have significantly shown… (more)

Subjects/Keywords: Electrochemical biosensors; Cytochrome P450-3A4 (CYP3A4); Horseradish peroxidase (HRP); ZnSe quantum dots; Conducting polymers; Cyclic voltammetry (CV); Differential-pulse voltammetry (DPV); 17- estradiol; 17α-ethnylestradiol; Estrogenic Endocrine Disrupting Compounds (e-EDC); Michaelis Menten constant; Hydroxylation

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

APA (6th Edition):

Jijana, A. N. (2010). Development of electrochemical ZnSe Quantam dots biosensors for low-level detection of 17β-Estradiol estrogenic endocrine disrupting compound . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/2310

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):

Jijana, Abongile Nwabisa. “Development of electrochemical ZnSe Quantam dots biosensors for low-level detection of 17β-Estradiol estrogenic endocrine disrupting compound .” 2010. Thesis, University of the Western Cape. Accessed January 21, 2021. http://hdl.handle.net/11394/2310.

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

MLA Handbook (7th Edition):

Jijana, Abongile Nwabisa. “Development of electrochemical ZnSe Quantam dots biosensors for low-level detection of 17β-Estradiol estrogenic endocrine disrupting compound .” 2010. Web. 21 Jan 2021.

Vancouver:

Jijana AN. Development of electrochemical ZnSe Quantam dots biosensors for low-level detection of 17β-Estradiol estrogenic endocrine disrupting compound . [Internet] [Thesis]. University of the Western Cape; 2010. [cited 2021 Jan 21]. Available from: http://hdl.handle.net/11394/2310.

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

Council of Science Editors:

Jijana AN. Development of electrochemical ZnSe Quantam dots biosensors for low-level detection of 17β-Estradiol estrogenic endocrine disrupting compound . [Thesis]. University of the Western Cape; 2010. Available from: http://hdl.handle.net/11394/2310

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


University of Michigan

18. Dhaini, Hassan R. Cytochrome P450 CYP3A4 /5: A new prognostic factor for osteosarcoma.

Degree: PhD, Toxicology, 2002, University of Michigan

 Osteosarcoma is a primary malignancy of bone with a tendeney for early pulmonary metastasis. There is a need to identify patients who may benefit from… (more)

Subjects/Keywords: Cyp3a4/5; Cytochrome P450; Factor; New; Osteosarcoma; Prognostic

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APA (6th Edition):

Dhaini, H. R. (2002). Cytochrome P450 CYP3A4 /5: A new prognostic factor for osteosarcoma. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/131733

Chicago Manual of Style (16th Edition):

Dhaini, Hassan R. “Cytochrome P450 CYP3A4 /5: A new prognostic factor for osteosarcoma.” 2002. Doctoral Dissertation, University of Michigan. Accessed January 21, 2021. http://hdl.handle.net/2027.42/131733.

MLA Handbook (7th Edition):

Dhaini, Hassan R. “Cytochrome P450 CYP3A4 /5: A new prognostic factor for osteosarcoma.” 2002. Web. 21 Jan 2021.

Vancouver:

Dhaini HR. Cytochrome P450 CYP3A4 /5: A new prognostic factor for osteosarcoma. [Internet] [Doctoral dissertation]. University of Michigan; 2002. [cited 2021 Jan 21]. Available from: http://hdl.handle.net/2027.42/131733.

Council of Science Editors:

Dhaini HR. Cytochrome P450 CYP3A4 /5: A new prognostic factor for osteosarcoma. [Doctoral Dissertation]. University of Michigan; 2002. Available from: http://hdl.handle.net/2027.42/131733


University of the Western Cape

19. Rassie, Candice. Electrochemical cytochrome P450 enzymatic biosensors for the determination of the reactivity of TB drugs .

Degree: 2020, University of the Western Cape

 Tuberculosis (TB) remains a global epidemic despite the fact that treatment has been available since the 1950’s. This disease is highly contagious and spreads via… (more)

Subjects/Keywords: Biosensor; Cytochrome P450; CYP3A4; Drug Metabolism; Ethambutol; Isoniazid; Metallodendrimer; Phenotype; Polypropyleneimine; Pyrazinamide; Real Samples; Rifampicin; Tuberculosis

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APA (6th Edition):

Rassie, C. (2020). Electrochemical cytochrome P450 enzymatic biosensors for the determination of the reactivity of TB drugs . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/7235

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):

Rassie, Candice. “Electrochemical cytochrome P450 enzymatic biosensors for the determination of the reactivity of TB drugs .” 2020. Thesis, University of the Western Cape. Accessed January 21, 2021. http://hdl.handle.net/11394/7235.

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

MLA Handbook (7th Edition):

Rassie, Candice. “Electrochemical cytochrome P450 enzymatic biosensors for the determination of the reactivity of TB drugs .” 2020. Web. 21 Jan 2021.

Vancouver:

Rassie C. Electrochemical cytochrome P450 enzymatic biosensors for the determination of the reactivity of TB drugs . [Internet] [Thesis]. University of the Western Cape; 2020. [cited 2021 Jan 21]. Available from: http://hdl.handle.net/11394/7235.

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

Council of Science Editors:

Rassie C. Electrochemical cytochrome P450 enzymatic biosensors for the determination of the reactivity of TB drugs . [Thesis]. University of the Western Cape; 2020. Available from: http://hdl.handle.net/11394/7235

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

20. Rhieu, Steve. Electrochemical, biochemical, structural studies of cytochrome P450 monooxygenases involved in metabolism of vitamin D.

Degree: PhD, Biomedical Engineering, 2011, Brown University

 This dissertation examines two cytochrome P450 monooxygenases, namely CYP27B1 and CYP24A1, for their potential applications in biosensors and drug metabolism, respectively. First, the feasibility of… (more)

Subjects/Keywords: Cytochrome P450

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APA (6th Edition):

Rhieu, S. (2011). Electrochemical, biochemical, structural studies of cytochrome P450 monooxygenases involved in metabolism of vitamin D. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:11352/

Chicago Manual of Style (16th Edition):

Rhieu, Steve. “Electrochemical, biochemical, structural studies of cytochrome P450 monooxygenases involved in metabolism of vitamin D.” 2011. Doctoral Dissertation, Brown University. Accessed January 21, 2021. https://repository.library.brown.edu/studio/item/bdr:11352/.

MLA Handbook (7th Edition):

Rhieu, Steve. “Electrochemical, biochemical, structural studies of cytochrome P450 monooxygenases involved in metabolism of vitamin D.” 2011. Web. 21 Jan 2021.

Vancouver:

Rhieu S. Electrochemical, biochemical, structural studies of cytochrome P450 monooxygenases involved in metabolism of vitamin D. [Internet] [Doctoral dissertation]. Brown University; 2011. [cited 2021 Jan 21]. Available from: https://repository.library.brown.edu/studio/item/bdr:11352/.

Council of Science Editors:

Rhieu S. Electrochemical, biochemical, structural studies of cytochrome P450 monooxygenases involved in metabolism of vitamin D. [Doctoral Dissertation]. Brown University; 2011. Available from: https://repository.library.brown.edu/studio/item/bdr:11352/


North Carolina State University

21. Casabar, Richard. Endosulfan-alpha Induces CYP2B6 and CYP3A4 via the Pregnane X Receptor.

Degree: MS, Toxicology, 2006, North Carolina State University

 The purpose of this research was to establish the metabolic pathway of endosulfan in humans and to elucidate a potential mechanism for endosulfan's endocrine disruptive… (more)

Subjects/Keywords: endosulfan; metabolism; induction of CYP; cytochrome P450 enzymes; CYP2B6; PXR; P450; CYP3A4

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APA (6th Edition):

Casabar, R. (2006). Endosulfan-alpha Induces CYP2B6 and CYP3A4 via the Pregnane X Receptor. (Thesis). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/2291

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):

Casabar, Richard. “Endosulfan-alpha Induces CYP2B6 and CYP3A4 via the Pregnane X Receptor.” 2006. Thesis, North Carolina State University. Accessed January 21, 2021. http://www.lib.ncsu.edu/resolver/1840.16/2291.

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

MLA Handbook (7th Edition):

Casabar, Richard. “Endosulfan-alpha Induces CYP2B6 and CYP3A4 via the Pregnane X Receptor.” 2006. Web. 21 Jan 2021.

Vancouver:

Casabar R. Endosulfan-alpha Induces CYP2B6 and CYP3A4 via the Pregnane X Receptor. [Internet] [Thesis]. North Carolina State University; 2006. [cited 2021 Jan 21]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/2291.

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

Council of Science Editors:

Casabar R. Endosulfan-alpha Induces CYP2B6 and CYP3A4 via the Pregnane X Receptor. [Thesis]. North Carolina State University; 2006. Available from: http://www.lib.ncsu.edu/resolver/1840.16/2291

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


University of Western Ontario

22. 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 January 21, 2021. 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. 21 Jan 2021.

Vancouver:

Wilson A. Drug Response And Metabolism In Crohn's Disease. [Internet] [Thesis]. University of Western Ontario; 2018. [cited 2021 Jan 21]. 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


University of Helsinki

23. Kaartinen, Taavi. CYP2C19 Inhibition Lasts for more than 72 Hours after High-Dose Esomeprazole: Estimation of CYP2C19 Half-Life Using Pantoprazole as an in Vivo Probe.

Degree: Medicinska fakulteten, 2018, University of Helsinki

Protonipumpun estäjä omepratsolin S-isomeerin, esomepratsolin, on in vitro-tutkimuksissa osoitettu olevan lääkeaineiden metaboliaan osallistuvan sytokromi P450 CYP2C19-entsyymin mekanismiperustainen inhibiittori. CYP2C19 osallistuu maksassa lukuisten kliinisesti laajassa käytössä… (more)

Subjects/Keywords: sytokromi P450; CYP2C19; CYP3A4; CYP1A2; protonipumpun estäjä; esomepratsoli; pantopratsoli; midatsolaami; kofeiini; farmakokinetiikka; lääkeaineinteraktio; puoliintumisaika; metabolia; altistus; Cytochrome P-450 CYP2C19, Proton Pump Inhibitors, Pharmacokinetics, Drug Interactions; sytokromi P450; CYP2C19; CYP3A4; CYP1A2; protonipumpun estäjä; esomepratsoli; pantopratsoli; midatsolaami; kofeiini; farmakokinetiikka; lääkeaineinteraktio; puoliintumisaika; metabolia; altistus

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APA (6th Edition):

Kaartinen, T. (2018). CYP2C19 Inhibition Lasts for more than 72 Hours after High-Dose Esomeprazole: Estimation of CYP2C19 Half-Life Using Pantoprazole as an in Vivo Probe. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/235814

Chicago Manual of Style (16th Edition):

Kaartinen, Taavi. “CYP2C19 Inhibition Lasts for more than 72 Hours after High-Dose Esomeprazole: Estimation of CYP2C19 Half-Life Using Pantoprazole as an in Vivo Probe.” 2018. Masters Thesis, University of Helsinki. Accessed January 21, 2021. http://hdl.handle.net/10138/235814.

MLA Handbook (7th Edition):

Kaartinen, Taavi. “CYP2C19 Inhibition Lasts for more than 72 Hours after High-Dose Esomeprazole: Estimation of CYP2C19 Half-Life Using Pantoprazole as an in Vivo Probe.” 2018. Web. 21 Jan 2021.

Vancouver:

Kaartinen T. CYP2C19 Inhibition Lasts for more than 72 Hours after High-Dose Esomeprazole: Estimation of CYP2C19 Half-Life Using Pantoprazole as an in Vivo Probe. [Internet] [Masters thesis]. University of Helsinki; 2018. [cited 2021 Jan 21]. Available from: http://hdl.handle.net/10138/235814.

Council of Science Editors:

Kaartinen T. CYP2C19 Inhibition Lasts for more than 72 Hours after High-Dose Esomeprazole: Estimation of CYP2C19 Half-Life Using Pantoprazole as an in Vivo Probe. [Masters Thesis]. University of Helsinki; 2018. Available from: http://hdl.handle.net/10138/235814


Université de Montréal

24. Theodoropoulos, Catherine. Influence du système endocrinien de la vitamine D dans la régulation de la vitamine D3 25-hydroxylase CYP27A hépatique et intestinale chez l'humain et le rat.

Degree: 2003, Université de Montréal

Subjects/Keywords: Vitamine D₃; CYP27A (vitamine D₃ ₂₅₋hydroxylase₎; CYP24 (vitamine D₃₋₂₄x₋hydroxylase₎; CYP27B1 (vitamine D₃ ₁ x₋hydrolase₎; CYP3A4 (cyclochrome P450 3A4); Vitamin D₃; CYP27A (vitamin D₃ ₂₅₋hydroxylase₎; CYP24 (vitamin D₃₋₂₄x₋hydroxylase₎; CYP27B1 (vitamin D₃ ₁ x₋hydrolase₎; CYP3A4 (cyclochrome P450 3A4)

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APA (6th Edition):

Theodoropoulos, C. (2003). Influence du système endocrinien de la vitamine D dans la régulation de la vitamine D3 25-hydroxylase CYP27A hépatique et intestinale chez l'humain et le rat. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/6685

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):

Theodoropoulos, Catherine. “Influence du système endocrinien de la vitamine D dans la régulation de la vitamine D3 25-hydroxylase CYP27A hépatique et intestinale chez l'humain et le rat.” 2003. Thesis, Université de Montréal. Accessed January 21, 2021. http://hdl.handle.net/1866/6685.

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

MLA Handbook (7th Edition):

Theodoropoulos, Catherine. “Influence du système endocrinien de la vitamine D dans la régulation de la vitamine D3 25-hydroxylase CYP27A hépatique et intestinale chez l'humain et le rat.” 2003. Web. 21 Jan 2021.

Vancouver:

Theodoropoulos C. Influence du système endocrinien de la vitamine D dans la régulation de la vitamine D3 25-hydroxylase CYP27A hépatique et intestinale chez l'humain et le rat. [Internet] [Thesis]. Université de Montréal; 2003. [cited 2021 Jan 21]. Available from: http://hdl.handle.net/1866/6685.

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

Council of Science Editors:

Theodoropoulos C. Influence du système endocrinien de la vitamine D dans la régulation de la vitamine D3 25-hydroxylase CYP27A hépatique et intestinale chez l'humain et le rat. [Thesis]. Université de Montréal; 2003. Available from: http://hdl.handle.net/1866/6685

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


University of Manchester

25. Porro, Cristina Shino. Quantum mechanical/molecular mechanics studies of Cytochrome P450BM3.

Degree: PhD, 2011, University of Manchester

Cytochrome P450 (P450) enzymes are found in all kingdoms of life, catalysing a wide range of biosynthetic and metabolic processes. They are, in fact, of… (more)

Subjects/Keywords: 572.7; Cytochrome P450; P450 BM3; QM/MM

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

APA (6th Edition):

Porro, C. S. (2011). Quantum mechanical/molecular mechanics studies of Cytochrome P450BM3. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/quantum-mechanical – molecular-mechanics-studies-of-cytochrome-p450bm3(ad4255e7-b779-47a2-a2c5-8dbf6b603ca5).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.538423

Chicago Manual of Style (16th Edition):

Porro, Cristina Shino. “Quantum mechanical/molecular mechanics studies of Cytochrome P450BM3.” 2011. Doctoral Dissertation, University of Manchester. Accessed January 21, 2021. https://www.research.manchester.ac.uk/portal/en/theses/quantum-mechanical – molecular-mechanics-studies-of-cytochrome-p450bm3(ad4255e7-b779-47a2-a2c5-8dbf6b603ca5).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.538423.

MLA Handbook (7th Edition):

Porro, Cristina Shino. “Quantum mechanical/molecular mechanics studies of Cytochrome P450BM3.” 2011. Web. 21 Jan 2021.

Vancouver:

Porro CS. Quantum mechanical/molecular mechanics studies of Cytochrome P450BM3. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2021 Jan 21]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/quantum-mechanical – molecular-mechanics-studies-of-cytochrome-p450bm3(ad4255e7-b779-47a2-a2c5-8dbf6b603ca5).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.538423.

Council of Science Editors:

Porro CS. Quantum mechanical/molecular mechanics studies of Cytochrome P450BM3. [Doctoral Dissertation]. University of Manchester; 2011. Available from: https://www.research.manchester.ac.uk/portal/en/theses/quantum-mechanical – molecular-mechanics-studies-of-cytochrome-p450bm3(ad4255e7-b779-47a2-a2c5-8dbf6b603ca5).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.538423


Cornell University

26. Bardowell, Sabrina. The Role Of Vitamin E Hydroxylases In Vitamin E Metabolism And Status.

Degree: PhD, Nutrition, 2012, Cornell University

 Vitamin E is a group of compounds that are considered to be the most important lipophilic antioxidants, however there is still much unknown about the… (more)

Subjects/Keywords: vitamin E; cytochrome P450; metabolism

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

APA (6th Edition):

Bardowell, S. (2012). The Role Of Vitamin E Hydroxylases In Vitamin E Metabolism And Status. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/31140

Chicago Manual of Style (16th Edition):

Bardowell, Sabrina. “The Role Of Vitamin E Hydroxylases In Vitamin E Metabolism And Status.” 2012. Doctoral Dissertation, Cornell University. Accessed January 21, 2021. http://hdl.handle.net/1813/31140.

MLA Handbook (7th Edition):

Bardowell, Sabrina. “The Role Of Vitamin E Hydroxylases In Vitamin E Metabolism And Status.” 2012. Web. 21 Jan 2021.

Vancouver:

Bardowell S. The Role Of Vitamin E Hydroxylases In Vitamin E Metabolism And Status. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2021 Jan 21]. Available from: http://hdl.handle.net/1813/31140.

Council of Science Editors:

Bardowell S. The Role Of Vitamin E Hydroxylases In Vitamin E Metabolism And Status. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/31140


University of Guelph

27. Darch, Maryse. Role of the Cytochrome P450 2A5 in Bilirubin Metabolism and Clearance in C57BL/6 Mice.

Degree: MS, Department of Biomedical Sciences, 2016, University of Guelph

Cytochrome P450 2A5 (CYP2A5) is uniquely induced in response to liver injury, indicating that CYP2A5 may have a cytoprotective function. Others have proposed that CYP2A5… (more)

Subjects/Keywords: CYP2A5; Bilirubin; Cytochrome P450

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

APA (6th Edition):

Darch, M. (2016). Role of the Cytochrome P450 2A5 in Bilirubin Metabolism and Clearance in C57BL/6 Mice. (Masters Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9464

Chicago Manual of Style (16th Edition):

Darch, Maryse. “Role of the Cytochrome P450 2A5 in Bilirubin Metabolism and Clearance in C57BL/6 Mice.” 2016. Masters Thesis, University of Guelph. Accessed January 21, 2021. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9464.

MLA Handbook (7th Edition):

Darch, Maryse. “Role of the Cytochrome P450 2A5 in Bilirubin Metabolism and Clearance in C57BL/6 Mice.” 2016. Web. 21 Jan 2021.

Vancouver:

Darch M. Role of the Cytochrome P450 2A5 in Bilirubin Metabolism and Clearance in C57BL/6 Mice. [Internet] [Masters thesis]. University of Guelph; 2016. [cited 2021 Jan 21]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9464.

Council of Science Editors:

Darch M. Role of the Cytochrome P450 2A5 in Bilirubin Metabolism and Clearance in C57BL/6 Mice. [Masters Thesis]. University of Guelph; 2016. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9464


University of Manchester

28. Matthews, Sarah. Characterisation and Engineering of Alkene Producing P450 Peroxygenases for Bioenergy Applications.

Degree: 2017, University of Manchester

 OleTJE (CYP152L1) is a P450 peroxygenase that was first isolated from Jeotgalicoccus sp. 8456 in 2011. OleTJE is primarily a fatty acid decarboxylase, converting mid-chain… (more)

Subjects/Keywords: OleT; Cytochrome P450; Biofuels

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

APA (6th Edition):

Matthews, S. (2017). Characterisation and Engineering of Alkene Producing P450 Peroxygenases for Bioenergy Applications. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:308754

Chicago Manual of Style (16th Edition):

Matthews, Sarah. “Characterisation and Engineering of Alkene Producing P450 Peroxygenases for Bioenergy Applications.” 2017. Doctoral Dissertation, University of Manchester. Accessed January 21, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:308754.

MLA Handbook (7th Edition):

Matthews, Sarah. “Characterisation and Engineering of Alkene Producing P450 Peroxygenases for Bioenergy Applications.” 2017. Web. 21 Jan 2021.

Vancouver:

Matthews S. Characterisation and Engineering of Alkene Producing P450 Peroxygenases for Bioenergy Applications. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2021 Jan 21]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:308754.

Council of Science Editors:

Matthews S. Characterisation and Engineering of Alkene Producing P450 Peroxygenases for Bioenergy Applications. [Doctoral Dissertation]. University of Manchester; 2017. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:308754


University of Texas – Austin

29. Sunnadeniya, Rasika Mayanthi. Identification and functional analysis of betalain pathway genes.

Degree: PhD, Plant Biology, 2014, University of Texas – Austin

 Betalains, comprised of red betacyanins and yellow betaxanthins, are found in the single order, Caryophyllales, where most other flowering plants produce anthocyanins. They are derived… (more)

Subjects/Keywords: Betalain; Cytochrome P450; Anthocyanins

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

APA (6th Edition):

Sunnadeniya, R. M. (2014). Identification and functional analysis of betalain pathway genes. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46526

Chicago Manual of Style (16th Edition):

Sunnadeniya, Rasika Mayanthi. “Identification and functional analysis of betalain pathway genes.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed January 21, 2021. http://hdl.handle.net/2152/46526.

MLA Handbook (7th Edition):

Sunnadeniya, Rasika Mayanthi. “Identification and functional analysis of betalain pathway genes.” 2014. Web. 21 Jan 2021.

Vancouver:

Sunnadeniya RM. Identification and functional analysis of betalain pathway genes. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2021 Jan 21]. Available from: http://hdl.handle.net/2152/46526.

Council of Science Editors:

Sunnadeniya RM. Identification and functional analysis of betalain pathway genes. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/46526


Université de Montréal

30. Fleury, Isabelle. Polymorphismes dans des gènes de métabolisme des corticostéroïdes : rôle dans la réponse thérapeutique.

Degree: 2004, Université de Montréal

Subjects/Keywords: Pharmacogénétique; Leucémie lymphoblastique aiguë; Récepteur des glucocorticoïdes; Cytochrome P450 3A4; Bcl I; Arg23Lys; Asn363Ser; A-290G

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

APA (6th Edition):

Fleury, I. (2004). Polymorphismes dans des gènes de métabolisme des corticostéroïdes : rôle dans la réponse thérapeutique. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/14201

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):

Fleury, Isabelle. “Polymorphismes dans des gènes de métabolisme des corticostéroïdes : rôle dans la réponse thérapeutique.” 2004. Thesis, Université de Montréal. Accessed January 21, 2021. http://hdl.handle.net/1866/14201.

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

MLA Handbook (7th Edition):

Fleury, Isabelle. “Polymorphismes dans des gènes de métabolisme des corticostéroïdes : rôle dans la réponse thérapeutique.” 2004. Web. 21 Jan 2021.

Vancouver:

Fleury I. Polymorphismes dans des gènes de métabolisme des corticostéroïdes : rôle dans la réponse thérapeutique. [Internet] [Thesis]. Université de Montréal; 2004. [cited 2021 Jan 21]. Available from: http://hdl.handle.net/1866/14201.

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

Council of Science Editors:

Fleury I. Polymorphismes dans des gènes de métabolisme des corticostéroïdes : rôle dans la réponse thérapeutique. [Thesis]. Université de Montréal; 2004. Available from: http://hdl.handle.net/1866/14201

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

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