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You searched for subject:(Cytochrome P450 CYP ). Showing records 1 – 30 of 1378 total matches.

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University of Manchester

1. Driscoll, Max. Investigating orphan cytochromes P450 from Mycobacterium tuberculosis : the search for potential drug targets.

Degree: PhD, 2011, University of Manchester

 Tuberculosis (TB) is a disease that the World Health Organisation (WHO) regards as a global pandemic. There is a great need for new drugs to… (more)

Subjects/Keywords: 579; Tuberculosis; Mycobacterium; Mtb; P450; Cytochrome; CYP

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

APA (6th Edition):

Driscoll, M. (2011). Investigating orphan cytochromes P450 from Mycobacterium tuberculosis : the search for potential drug targets. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/investigating-orphan-cytochromes-p450-from-mycobacterium-tuberculosis-the-search-for-potential-drug-targets(58eef811-4e97-4bfa-83ba-46be1a48c9f5).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.538488

Chicago Manual of Style (16th Edition):

Driscoll, Max. “Investigating orphan cytochromes P450 from Mycobacterium tuberculosis : the search for potential drug targets.” 2011. Doctoral Dissertation, University of Manchester. Accessed April 17, 2021. https://www.research.manchester.ac.uk/portal/en/theses/investigating-orphan-cytochromes-p450-from-mycobacterium-tuberculosis-the-search-for-potential-drug-targets(58eef811-4e97-4bfa-83ba-46be1a48c9f5).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.538488.

MLA Handbook (7th Edition):

Driscoll, Max. “Investigating orphan cytochromes P450 from Mycobacterium tuberculosis : the search for potential drug targets.” 2011. Web. 17 Apr 2021.

Vancouver:

Driscoll M. Investigating orphan cytochromes P450 from Mycobacterium tuberculosis : the search for potential drug targets. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2021 Apr 17]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/investigating-orphan-cytochromes-p450-from-mycobacterium-tuberculosis-the-search-for-potential-drug-targets(58eef811-4e97-4bfa-83ba-46be1a48c9f5).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.538488.

Council of Science Editors:

Driscoll M. Investigating orphan cytochromes P450 from Mycobacterium tuberculosis : the search for potential drug targets. [Doctoral Dissertation]. University of Manchester; 2011. Available from: https://www.research.manchester.ac.uk/portal/en/theses/investigating-orphan-cytochromes-p450-from-mycobacterium-tuberculosis-the-search-for-potential-drug-targets(58eef811-4e97-4bfa-83ba-46be1a48c9f5).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.538488

2. 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 April 17, 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. 17 Apr 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 Apr 17]. 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


University of North Texas

3. Quan, Daniel L. Cytochrome P450 Gene Expression Modulates Anoxia Sensitivity in Caenorhabditis Elegans.

Degree: 2016, University of North Texas

 With an increasing population suffering from obesity or Diabetes Mellitus (DM), it is more pertinent than ever to understand how physiological changes impact cellular processes.… (more)

Subjects/Keywords: Caenhorhabditis elegans; Cytochrome P450; CYP; cyp-33C8; hsp-4::GFP; Biology, Genetics

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APA (6th Edition):

Quan, D. L. (2016). Cytochrome P450 Gene Expression Modulates Anoxia Sensitivity in Caenorhabditis Elegans. (Thesis). University of North Texas. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc862757/

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):

Quan, Daniel L. “Cytochrome P450 Gene Expression Modulates Anoxia Sensitivity in Caenorhabditis Elegans.” 2016. Thesis, University of North Texas. Accessed April 17, 2021. https://digital.library.unt.edu/ark:/67531/metadc862757/.

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

MLA Handbook (7th Edition):

Quan, Daniel L. “Cytochrome P450 Gene Expression Modulates Anoxia Sensitivity in Caenorhabditis Elegans.” 2016. Web. 17 Apr 2021.

Vancouver:

Quan DL. Cytochrome P450 Gene Expression Modulates Anoxia Sensitivity in Caenorhabditis Elegans. [Internet] [Thesis]. University of North Texas; 2016. [cited 2021 Apr 17]. Available from: https://digital.library.unt.edu/ark:/67531/metadc862757/.

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

Council of Science Editors:

Quan DL. Cytochrome P450 Gene Expression Modulates Anoxia Sensitivity in Caenorhabditis Elegans. [Thesis]. University of North Texas; 2016. Available from: https://digital.library.unt.edu/ark:/67531/metadc862757/

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


Rice University

4. Castillo-Rivera, Dorianne A. A Journey through the Arabidopsis thaliana Genome: Discovering the Origins of Novel Triterpene Metabolites.

Degree: PhD, Natural Sciences, 2014, Rice University

 Plants produce a large variety of natural products, including over 20,000 different triterpenoids. Triterpenoid functions range from roles as membrane sterols and hormones in primary… (more)

Subjects/Keywords: triterpene; triterpenoids; CYP; cytochrome P450; arabidopsis thaliana; metabolism; genome mining; OSC

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APA (6th Edition):

Castillo-Rivera, D. A. (2014). A Journey through the Arabidopsis thaliana Genome: Discovering the Origins of Novel Triterpene Metabolites. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/95524

Chicago Manual of Style (16th Edition):

Castillo-Rivera, Dorianne A. “A Journey through the Arabidopsis thaliana Genome: Discovering the Origins of Novel Triterpene Metabolites.” 2014. Doctoral Dissertation, Rice University. Accessed April 17, 2021. http://hdl.handle.net/1911/95524.

MLA Handbook (7th Edition):

Castillo-Rivera, Dorianne A. “A Journey through the Arabidopsis thaliana Genome: Discovering the Origins of Novel Triterpene Metabolites.” 2014. Web. 17 Apr 2021.

Vancouver:

Castillo-Rivera DA. A Journey through the Arabidopsis thaliana Genome: Discovering the Origins of Novel Triterpene Metabolites. [Internet] [Doctoral dissertation]. Rice University; 2014. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/1911/95524.

Council of Science Editors:

Castillo-Rivera DA. A Journey through the Arabidopsis thaliana Genome: Discovering the Origins of Novel Triterpene Metabolites. [Doctoral Dissertation]. Rice University; 2014. Available from: http://hdl.handle.net/1911/95524


University of Vienna

5. Zehetner, Petra. Essential oil components and CYP-enzymes.

Degree: 2019, University of Vienna

Die Hauptroute für die Elimination von vielen Medikamenten stellt der von Cytochrom P450 (CYP) Enzymen durchgeführte Phase I Metabolismus dar. Da die Bioaktivität von ätherischen… (more)

Subjects/Keywords: 44.42 Pharmazeutische Chemie; Cytochrom P450 / CYP-Induktion / CYP-Inhibition / Ätherische Öl Komponenten / Metabolismus / Biotransformation von Xenobiotika; Cytochrome P450 / CYP-induction / CYP-inhibition / essential oil constituents / metabolism / biotransformation of xenobiotics

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APA (6th Edition):

Zehetner, P. (2019). Essential oil components and CYP-enzymes. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/57094/

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):

Zehetner, Petra. “Essential oil components and CYP-enzymes.” 2019. Thesis, University of Vienna. Accessed April 17, 2021. http://othes.univie.ac.at/57094/.

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

MLA Handbook (7th Edition):

Zehetner, Petra. “Essential oil components and CYP-enzymes.” 2019. Web. 17 Apr 2021.

Vancouver:

Zehetner P. Essential oil components and CYP-enzymes. [Internet] [Thesis]. University of Vienna; 2019. [cited 2021 Apr 17]. Available from: http://othes.univie.ac.at/57094/.

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

Council of Science Editors:

Zehetner P. Essential oil components and CYP-enzymes. [Thesis]. University of Vienna; 2019. Available from: http://othes.univie.ac.at/57094/

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


McMaster University

6. Dejong, Christopher A. THE CYTOCHROME P450 SUPERFAMILY COMPLEMENT (CYPome) IN THE ANNELID CAPITELLA TELETA.

Degree: MSc, 2013, McMaster University

CYPs are a large and diverse protein superfamily found in all domains of life and are able to metabolize a wide array of both… (more)

Subjects/Keywords: Cytochrome P450; Capitella Teleta; CYPome; CYP; Sterodogenesis in Annelids; Xenobiotic Metabolism; Bioinformatics; Biology; Bioinformatics

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APA (6th Edition):

Dejong, C. A. (2013). THE CYTOCHROME P450 SUPERFAMILY COMPLEMENT (CYPome) IN THE ANNELID CAPITELLA TELETA. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/13581

Chicago Manual of Style (16th Edition):

Dejong, Christopher A. “THE CYTOCHROME P450 SUPERFAMILY COMPLEMENT (CYPome) IN THE ANNELID CAPITELLA TELETA.” 2013. Masters Thesis, McMaster University. Accessed April 17, 2021. http://hdl.handle.net/11375/13581.

MLA Handbook (7th Edition):

Dejong, Christopher A. “THE CYTOCHROME P450 SUPERFAMILY COMPLEMENT (CYPome) IN THE ANNELID CAPITELLA TELETA.” 2013. Web. 17 Apr 2021.

Vancouver:

Dejong CA. THE CYTOCHROME P450 SUPERFAMILY COMPLEMENT (CYPome) IN THE ANNELID CAPITELLA TELETA. [Internet] [Masters thesis]. McMaster University; 2013. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11375/13581.

Council of Science Editors:

Dejong CA. THE CYTOCHROME P450 SUPERFAMILY COMPLEMENT (CYPome) IN THE ANNELID CAPITELLA TELETA. [Masters Thesis]. McMaster University; 2013. Available from: http://hdl.handle.net/11375/13581

7. Siqueira, Carolina Morse. Efeito da pentoxifilina sobre as enzimas demetabolismo de xenobióticos na malária murina causadapelo Plasmodium berghei ANKA e no modelo de sepsecausada pelo LPS de Escherichia coli.

Degree: 2014, Brazil

Submitted by Gilvan Almeida ([email protected]) on 2016-08-10T18:28:02Z No. of bitstreams: 2 208.pdf: 1811695 bytes, checksum: 161bc5072a707cd91c96c2b47a631b9b (MD5) license.txt: 1748 bytes, checksum: 8a4605be74aa9ea9d79846c1fba20a33 (MD5)

Approved for… (more)

Subjects/Keywords: Citocromo P450; CYP; Plasmodium Berghei ANKA; Malária; Xenobióticos; Cytochrome P450; CYP; Plasmodium Berghei ANKA; Malaria; Xenobiotics; Malária/epidemiologia; Biotransformação; Sistema Enzimático do Citocromo P-450; Escherichia coli/metabolismo; Xenobióticos

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APA (6th Edition):

Siqueira, C. M. (2014). Efeito da pentoxifilina sobre as enzimas demetabolismo de xenobióticos na malária murina causadapelo Plasmodium berghei ANKA e no modelo de sepsecausada pelo LPS de Escherichia coli. (Masters Thesis). Brazil. Retrieved from https://www.arca.fiocruz.br/handle/icict/24312

Chicago Manual of Style (16th Edition):

Siqueira, Carolina Morse. “Efeito da pentoxifilina sobre as enzimas demetabolismo de xenobióticos na malária murina causadapelo Plasmodium berghei ANKA e no modelo de sepsecausada pelo LPS de Escherichia coli.” 2014. Masters Thesis, Brazil. Accessed April 17, 2021. https://www.arca.fiocruz.br/handle/icict/24312.

MLA Handbook (7th Edition):

Siqueira, Carolina Morse. “Efeito da pentoxifilina sobre as enzimas demetabolismo de xenobióticos na malária murina causadapelo Plasmodium berghei ANKA e no modelo de sepsecausada pelo LPS de Escherichia coli.” 2014. Web. 17 Apr 2021.

Vancouver:

Siqueira CM. Efeito da pentoxifilina sobre as enzimas demetabolismo de xenobióticos na malária murina causadapelo Plasmodium berghei ANKA e no modelo de sepsecausada pelo LPS de Escherichia coli. [Internet] [Masters thesis]. Brazil; 2014. [cited 2021 Apr 17]. Available from: https://www.arca.fiocruz.br/handle/icict/24312.

Council of Science Editors:

Siqueira CM. Efeito da pentoxifilina sobre as enzimas demetabolismo de xenobióticos na malária murina causadapelo Plasmodium berghei ANKA e no modelo de sepsecausada pelo LPS de Escherichia coli. [Masters Thesis]. Brazil; 2014. Available from: https://www.arca.fiocruz.br/handle/icict/24312

8. Driscoll, Max. Investigating orphan cytochromes P450 from Mycobacterium tuberculosis: The search for potential drug targets.

Degree: 2011, University of Manchester

 Tuberculosis (TB) is a disease that the World Health Organisation (WHO)regards as a global pandemic. There is a great need for new drugs to combat… (more)

Subjects/Keywords: Tuberculosis; Mycobacterium; Mtb; P450; Cytochrome; CYP

…Amp BCG bp BTZ Cm CO CPB CPD CSF CT CYP or P450 cYY DNA DOTS EMB EPR ETH FAD FDR FDX FMN FQ… …Cytochrome P450 Cyclo-L-Tyr-L-Tyr Deoxyribonucleic acid Direct observed therapy scheme Ethambutol… …P450 (CYP) enzymes [Cole, S. T. et al. 1998]. These mono-oxygenase… …Mycobacterium tuberculosis Cytochrome P450 CYP144: Solving crystallographic problems using molecular… …Key features of CYP144 and other major Mycobacterium tuberculosis 161 P450 enzymes Chapter… 

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

APA (6th Edition):

Driscoll, M. (2011). Investigating orphan cytochromes P450 from Mycobacterium tuberculosis: The search for potential drug targets. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:122243

Chicago Manual of Style (16th Edition):

Driscoll, Max. “Investigating orphan cytochromes P450 from Mycobacterium tuberculosis: The search for potential drug targets.” 2011. Doctoral Dissertation, University of Manchester. Accessed April 17, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:122243.

MLA Handbook (7th Edition):

Driscoll, Max. “Investigating orphan cytochromes P450 from Mycobacterium tuberculosis: The search for potential drug targets.” 2011. Web. 17 Apr 2021.

Vancouver:

Driscoll M. Investigating orphan cytochromes P450 from Mycobacterium tuberculosis: The search for potential drug targets. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2021 Apr 17]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:122243.

Council of Science Editors:

Driscoll M. Investigating orphan cytochromes P450 from Mycobacterium tuberculosis: The search for potential drug targets. [Doctoral Dissertation]. University of Manchester; 2011. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:122243


Freie Universität Berlin

9. Preißner, Saskia Maria. effect and metabolism.

Degree: 2011, Freie Universität Berlin

 Xenobiotics are substances, which cannot be synthesized by the metabolism of the human body, but are ingested as drugs or food. This work deals with… (more)

Subjects/Keywords: cytochrome P450 enzymes; CYP; artificial sweeteners; metabolism; xenobiotics; cancer therapy; target molecules; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Preißner, S. M. (2011). effect and metabolism. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/11451

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):

Preißner, Saskia Maria. “effect and metabolism.” 2011. Thesis, Freie Universität Berlin. Accessed April 17, 2021. https://refubium.fu-berlin.de/handle/fub188/11451.

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

MLA Handbook (7th Edition):

Preißner, Saskia Maria. “effect and metabolism.” 2011. Web. 17 Apr 2021.

Vancouver:

Preißner SM. effect and metabolism. [Internet] [Thesis]. Freie Universität Berlin; 2011. [cited 2021 Apr 17]. Available from: https://refubium.fu-berlin.de/handle/fub188/11451.

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

Council of Science Editors:

Preißner SM. effect and metabolism. [Thesis]. Freie Universität Berlin; 2011. Available from: https://refubium.fu-berlin.de/handle/fub188/11451

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


Freie Universität Berlin

10. Hoffmann, Michael. Xenobiotics: Interactions and alterartions in human metabolism.

Degree: 2015, Freie Universität Berlin

 The number of prescribed drugs is rising constantly. Nowadays, many patients are at risk as a result of polypharmacy. The occurrence of undesirable side effects… (more)

Subjects/Keywords: side effects; biotransformation; Cytochrome P450; CYP; food interactions, xenobiotics; polypharmacy; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Hoffmann, M. (2015). Xenobiotics: Interactions and alterartions in human metabolism. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-12496

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):

Hoffmann, Michael. “Xenobiotics: Interactions and alterartions in human metabolism.” 2015. Thesis, Freie Universität Berlin. Accessed April 17, 2021. http://dx.doi.org/10.17169/refubium-12496.

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

MLA Handbook (7th Edition):

Hoffmann, Michael. “Xenobiotics: Interactions and alterartions in human metabolism.” 2015. Web. 17 Apr 2021.

Vancouver:

Hoffmann M. Xenobiotics: Interactions and alterartions in human metabolism. [Internet] [Thesis]. Freie Universität Berlin; 2015. [cited 2021 Apr 17]. Available from: http://dx.doi.org/10.17169/refubium-12496.

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

Council of Science Editors:

Hoffmann M. Xenobiotics: Interactions and alterartions in human metabolism. [Thesis]. Freie Universität Berlin; 2015. Available from: http://dx.doi.org/10.17169/refubium-12496

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


Freie Universität Berlin

11. Zhu, Ye. Rolle von Cytochrom P450 (CYP) -abhängigen Eicosanoide bei der experimentellen akuten Nierenschädigung (AKI).

Degree: 2015, Freie Universität Berlin

 Hintergrund und Hypothese: Ischämie-bedingtes akutes Nierenversagen (ANV) kann als schwerwiegende Komplikation in verschiedenen klinischen Situationen auftreten und führt zu erhöhter Morbidität und Mortalität der Patienten.… (more)

Subjects/Keywords: cytochrome P450 (CYP); dependent eicosanoids; acute kidney injury (AKI); 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Zhu, Y. (2015). Rolle von Cytochrom P450 (CYP) -abhängigen Eicosanoide bei der experimentellen akuten Nierenschädigung (AKI). (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-6041

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):

Zhu, Ye. “Rolle von Cytochrom P450 (CYP) -abhängigen Eicosanoide bei der experimentellen akuten Nierenschädigung (AKI).” 2015. Thesis, Freie Universität Berlin. Accessed April 17, 2021. http://dx.doi.org/10.17169/refubium-6041.

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

MLA Handbook (7th Edition):

Zhu, Ye. “Rolle von Cytochrom P450 (CYP) -abhängigen Eicosanoide bei der experimentellen akuten Nierenschädigung (AKI).” 2015. Web. 17 Apr 2021.

Vancouver:

Zhu Y. Rolle von Cytochrom P450 (CYP) -abhängigen Eicosanoide bei der experimentellen akuten Nierenschädigung (AKI). [Internet] [Thesis]. Freie Universität Berlin; 2015. [cited 2021 Apr 17]. Available from: http://dx.doi.org/10.17169/refubium-6041.

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

Council of Science Editors:

Zhu Y. Rolle von Cytochrom P450 (CYP) -abhängigen Eicosanoide bei der experimentellen akuten Nierenschädigung (AKI). [Thesis]. Freie Universität Berlin; 2015. Available from: http://dx.doi.org/10.17169/refubium-6041

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


University of Bradford

12. Abumansour, Hamza M. A. Quantitative pharmacoproteomics investigation of anti-cancer drugs in mouse : development and optimisation of proteomics workflows for evaluating the effect of anti-cancer drugs on mouse liver.

Degree: PhD, 2016, University of Bradford

 Minimizing anti-cancer drug toxicity is a major challenge for the pharmaceutical industry. Toxicity is most frequently due to either the direct interaction of the drug… (more)

Subjects/Keywords: 570; Pharmacoproteomics; Anti-cancer drugs; Shotgun; Mass spectrometry; Drug toxicity; Mouse liver; Drug-induced liver injury; Pheromone; Cytochrome P450 (CYP)

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APA (6th Edition):

Abumansour, H. M. A. (2016). Quantitative pharmacoproteomics investigation of anti-cancer drugs in mouse : development and optimisation of proteomics workflows for evaluating the effect of anti-cancer drugs on mouse liver. (Doctoral Dissertation). University of Bradford. Retrieved from http://hdl.handle.net/10454/15724

Chicago Manual of Style (16th Edition):

Abumansour, Hamza M A. “Quantitative pharmacoproteomics investigation of anti-cancer drugs in mouse : development and optimisation of proteomics workflows for evaluating the effect of anti-cancer drugs on mouse liver.” 2016. Doctoral Dissertation, University of Bradford. Accessed April 17, 2021. http://hdl.handle.net/10454/15724.

MLA Handbook (7th Edition):

Abumansour, Hamza M A. “Quantitative pharmacoproteomics investigation of anti-cancer drugs in mouse : development and optimisation of proteomics workflows for evaluating the effect of anti-cancer drugs on mouse liver.” 2016. Web. 17 Apr 2021.

Vancouver:

Abumansour HMA. Quantitative pharmacoproteomics investigation of anti-cancer drugs in mouse : development and optimisation of proteomics workflows for evaluating the effect of anti-cancer drugs on mouse liver. [Internet] [Doctoral dissertation]. University of Bradford; 2016. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/10454/15724.

Council of Science Editors:

Abumansour HMA. Quantitative pharmacoproteomics investigation of anti-cancer drugs in mouse : development and optimisation of proteomics workflows for evaluating the effect of anti-cancer drugs on mouse liver. [Doctoral Dissertation]. University of Bradford; 2016. Available from: http://hdl.handle.net/10454/15724

13. Alves, Paula Daniela Souza. Estudo do papel das células de Kupffer na modulação dos citocromos P450 hepáticos por estímulos inflamatórios.

Degree: 2016, Brazil

Submitted by Angelo Silva ([email protected]) on 2017-03-30T17:22:47Z No. of bitstreams: 2 license.txt: 1748 bytes, checksum: 8a4605be74aa9ea9d79846c1fba20a33 (MD5) 65.pdf: 3166073 bytes, checksum: e5566110b92946f93c49ff15ac3924ff (MD5)

Approved for… (more)

Subjects/Keywords: GdCl3; Células de Kupffer; Citocromo P450; CYP; CYP1A; GdCl3; Kupffer Cell; Cytochrome P45; CYP; CYP1A; Macrófagos do Fígado/enzimologia; Sistema Enzimático do Citocromo P-450; Xenobióticos/metabolismo; Fígado/enzimologia

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APA (6th Edition):

Alves, P. D. S. (2016). Estudo do papel das células de Kupffer na modulação dos citocromos P450 hepáticos por estímulos inflamatórios. (Masters Thesis). Brazil. Retrieved from https://www.arca.fiocruz.br/handle/icict/20593

Chicago Manual of Style (16th Edition):

Alves, Paula Daniela Souza. “Estudo do papel das células de Kupffer na modulação dos citocromos P450 hepáticos por estímulos inflamatórios.” 2016. Masters Thesis, Brazil. Accessed April 17, 2021. https://www.arca.fiocruz.br/handle/icict/20593.

MLA Handbook (7th Edition):

Alves, Paula Daniela Souza. “Estudo do papel das células de Kupffer na modulação dos citocromos P450 hepáticos por estímulos inflamatórios.” 2016. Web. 17 Apr 2021.

Vancouver:

Alves PDS. Estudo do papel das células de Kupffer na modulação dos citocromos P450 hepáticos por estímulos inflamatórios. [Internet] [Masters thesis]. Brazil; 2016. [cited 2021 Apr 17]. Available from: https://www.arca.fiocruz.br/handle/icict/20593.

Council of Science Editors:

Alves PDS. Estudo do papel das células de Kupffer na modulação dos citocromos P450 hepáticos por estímulos inflamatórios. [Masters Thesis]. Brazil; 2016. Available from: https://www.arca.fiocruz.br/handle/icict/20593

14. 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 April 17, 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. 17 Apr 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 Apr 17]. 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

15. 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 April 17, 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. 17 Apr 2021.

Vancouver:

Casabar R. Endosulfan-alpha Induces CYP2B6 and CYP3A4 via the Pregnane X Receptor. [Internet] [Thesis]. North Carolina State University; 2006. [cited 2021 Apr 17]. 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


Freie Universität Berlin

16. Preißner, Sarah. Analysis of interactions and polymorphisms of xenobiotic enzymes for optimization of the medication and an exemplary application in polychemotherapy.

Degree: 2015, Freie Universität Berlin

 More than half of the people aged 50 years or older are administered at least five drugs daily. The enzymes, which are responsible for the… (more)

Subjects/Keywords: personalized medicine; CYP; cytochrome P450; chemotherapy; transporter; drug-drug-interactions; drug enzyme interactions; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Preißner, S. (2015). Analysis of interactions and polymorphisms of xenobiotic enzymes for optimization of the medication and an exemplary application in polychemotherapy. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/10575

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):

Preißner, Sarah. “Analysis of interactions and polymorphisms of xenobiotic enzymes for optimization of the medication and an exemplary application in polychemotherapy.” 2015. Thesis, Freie Universität Berlin. Accessed April 17, 2021. https://refubium.fu-berlin.de/handle/fub188/10575.

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

MLA Handbook (7th Edition):

Preißner, Sarah. “Analysis of interactions and polymorphisms of xenobiotic enzymes for optimization of the medication and an exemplary application in polychemotherapy.” 2015. Web. 17 Apr 2021.

Vancouver:

Preißner S. Analysis of interactions and polymorphisms of xenobiotic enzymes for optimization of the medication and an exemplary application in polychemotherapy. [Internet] [Thesis]. Freie Universität Berlin; 2015. [cited 2021 Apr 17]. Available from: https://refubium.fu-berlin.de/handle/fub188/10575.

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

Council of Science Editors:

Preißner S. Analysis of interactions and polymorphisms of xenobiotic enzymes for optimization of the medication and an exemplary application in polychemotherapy. [Thesis]. Freie Universität Berlin; 2015. Available from: https://refubium.fu-berlin.de/handle/fub188/10575

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


University of Illinois – Urbana-Champaign

17. Meyer, Michael D. Studies on sweet corn: Stewart's wilt forecasting, the effect of maize dwarf mosaic on foliar diseases, and herbicide sensitivity.

Degree: MS, 0030, 2010, University of Illinois – Urbana-Champaign

 Diseases and sensitivity to P450-metabolized herbicides can limit the production of high quality sweet corn. Separate studies were done to determine the probability of exceeding… (more)

Subjects/Keywords: Sweet corn; Zea mays; corn diseases; Maize dwarf mosaic; Stewart's wilt; herbicide sensitivity; yield; cytochrome P450 (CYP); CYP genes

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APA (6th Edition):

Meyer, M. D. (2010). Studies on sweet corn: Stewart's wilt forecasting, the effect of maize dwarf mosaic on foliar diseases, and herbicide sensitivity. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/16014

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):

Meyer, Michael D. “Studies on sweet corn: Stewart's wilt forecasting, the effect of maize dwarf mosaic on foliar diseases, and herbicide sensitivity.” 2010. Thesis, University of Illinois – Urbana-Champaign. Accessed April 17, 2021. http://hdl.handle.net/2142/16014.

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

MLA Handbook (7th Edition):

Meyer, Michael D. “Studies on sweet corn: Stewart's wilt forecasting, the effect of maize dwarf mosaic on foliar diseases, and herbicide sensitivity.” 2010. Web. 17 Apr 2021.

Vancouver:

Meyer MD. Studies on sweet corn: Stewart's wilt forecasting, the effect of maize dwarf mosaic on foliar diseases, and herbicide sensitivity. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2010. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/2142/16014.

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

Council of Science Editors:

Meyer MD. Studies on sweet corn: Stewart's wilt forecasting, the effect of maize dwarf mosaic on foliar diseases, and herbicide sensitivity. [Thesis]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/16014

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


University of Vienna

18. Labuz, Dominik. Prediction of competitive CYP450 2C19 inhibitors using 3D pharmacophore modeling.

Degree: 2019, University of Vienna

Die Cytochrom P450 Enzyme mit ihrer einzigartigen prosthetischen Häm Gruppe in deren aktivem Zentrum gehören zu den wichtigsten Abwehrsystemen im menschlichen Organismus. Sie sind für… (more)

Subjects/Keywords: 44.40 Pharmazie, Pharmazeutika; 44.42 Pharmazeutische Chemie; 35.06 Computeranwendungen; Cytochrom P450 / CYP 2C19 Inhibitoren / Pharmakophor Modeling / LigandScout / Ligandenbasiertes Modeling / Strukturbasiertes Modeling / Virtuelles Screening / ChEMBL-Datenbank / Protein Datenbank / Knime; Cytochrome P450 / CYP 2C19 Inhibitors / Pharmacophore Modeling / LigandScout / Ligand-based Modeling / Structure-based Modeling / Virtual Screening / ChEMBL-Database / Protein Data Bank / Knime

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APA (6th Edition):

Labuz, D. (2019). Prediction of competitive CYP450 2C19 inhibitors using 3D pharmacophore modeling. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/58631/

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):

Labuz, Dominik. “Prediction of competitive CYP450 2C19 inhibitors using 3D pharmacophore modeling.” 2019. Thesis, University of Vienna. Accessed April 17, 2021. http://othes.univie.ac.at/58631/.

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

MLA Handbook (7th Edition):

Labuz, Dominik. “Prediction of competitive CYP450 2C19 inhibitors using 3D pharmacophore modeling.” 2019. Web. 17 Apr 2021.

Vancouver:

Labuz D. Prediction of competitive CYP450 2C19 inhibitors using 3D pharmacophore modeling. [Internet] [Thesis]. University of Vienna; 2019. [cited 2021 Apr 17]. Available from: http://othes.univie.ac.at/58631/.

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

Council of Science Editors:

Labuz D. Prediction of competitive CYP450 2C19 inhibitors using 3D pharmacophore modeling. [Thesis]. University of Vienna; 2019. Available from: http://othes.univie.ac.at/58631/

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


University of Manchester

19. 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 (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 April 17, 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. 17 Apr 2021.

Vancouver:

Porro CS. Quantum mechanical/molecular mechanics studies of Cytochrome P450BM3. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2021 Apr 17]. 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


University of Utah

20. 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 (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 April 17, 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. 17 Apr 2021.

Vancouver:

Moore CD. Dehydrogenation of Raloxifene by Cytochrome P450 3A4. [Internet] [Doctoral dissertation]. University of Utah; 2010. [cited 2021 Apr 17]. 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


Cornell University

21. 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 (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 April 17, 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. 17 Apr 2021.

Vancouver:

Bardowell S. The Role Of Vitamin E Hydroxylases In Vitamin E Metabolism And Status. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2021 Apr 17]. 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

22. 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 (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 April 17, 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. 17 Apr 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 Apr 17]. 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

23. 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 (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 April 17, 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. 17 Apr 2021.

Vancouver:

Matthews S. Characterisation and Engineering of Alkene Producing P450 Peroxygenases for Bioenergy Applications. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2021 Apr 17]. 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

24. 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 (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 April 17, 2021. http://hdl.handle.net/2152/46526.

MLA Handbook (7th Edition):

Sunnadeniya, Rasika Mayanthi. “Identification and functional analysis of betalain pathway genes.” 2014. Web. 17 Apr 2021.

Vancouver:

Sunnadeniya RM. Identification and functional analysis of betalain pathway genes. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2021 Apr 17]. 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


University of Illinois – Urbana-Champaign

25. Duggal, Ruchia. Mechanistic investigation of human cytochromes P450 involved in hormone biosynthesis.

Degree: PhD, Biochemistry, 2017, University of Illinois – Urbana-Champaign

 CYP17A1 and CYP19A1 are the key cytochromes P450 involved in steroidogenesis. Mutations causing hypo- or hyper-activation of both these enzymes results in diseased states, including… (more)

Subjects/Keywords: Cytochrome P450 17A1 (CYP17A1); Cytochrome b5; CYP19A1

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APA (6th Edition):

Duggal, R. (2017). Mechanistic investigation of human cytochromes P450 involved in hormone biosynthesis. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/99474

Chicago Manual of Style (16th Edition):

Duggal, Ruchia. “Mechanistic investigation of human cytochromes P450 involved in hormone biosynthesis.” 2017. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed April 17, 2021. http://hdl.handle.net/2142/99474.

MLA Handbook (7th Edition):

Duggal, Ruchia. “Mechanistic investigation of human cytochromes P450 involved in hormone biosynthesis.” 2017. Web. 17 Apr 2021.

Vancouver:

Duggal R. Mechanistic investigation of human cytochromes P450 involved in hormone biosynthesis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2017. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/2142/99474.

Council of Science Editors:

Duggal R. Mechanistic investigation of human cytochromes P450 involved in hormone biosynthesis. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2017. Available from: http://hdl.handle.net/2142/99474

26. Quesnot, Nicolas. Évaluation de la génotoxicité des contaminants environnementaux, production de lignées bio-senseurs et mesure de l'activité enzymatique du cytochrome P450 2E1 dans les cellules d'hépatome humain HepaRG : Evaluation of genotoxicity of environmental contaminants,production of bio-sensor cell lines and measurment of CYP2E1 enzymatic activity.

Degree: Docteur es, Biologie et sciences de la santé, 2015, Rennes 1

 L'exposition humaine aux contaminants environnementaux est inévitable du fait de leur présence dans l'eau, l'air et l'alimentation. La plupart d'entre eux sont reconnus comme étant… (more)

Subjects/Keywords: Cytochrome P450; Cyp2e1; Génotoxicité; Chlorzoxazone; Cytochrome P450; Cyp2e1; Genotoxicity; Chlorzoxazone

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

APA (6th Edition):

Quesnot, N. (2015). Évaluation de la génotoxicité des contaminants environnementaux, production de lignées bio-senseurs et mesure de l'activité enzymatique du cytochrome P450 2E1 dans les cellules d'hépatome humain HepaRG : Evaluation of genotoxicity of environmental contaminants,production of bio-sensor cell lines and measurment of CYP2E1 enzymatic activity. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2015REN1B005

Chicago Manual of Style (16th Edition):

Quesnot, Nicolas. “Évaluation de la génotoxicité des contaminants environnementaux, production de lignées bio-senseurs et mesure de l'activité enzymatique du cytochrome P450 2E1 dans les cellules d'hépatome humain HepaRG : Evaluation of genotoxicity of environmental contaminants,production of bio-sensor cell lines and measurment of CYP2E1 enzymatic activity.” 2015. Doctoral Dissertation, Rennes 1. Accessed April 17, 2021. http://www.theses.fr/2015REN1B005.

MLA Handbook (7th Edition):

Quesnot, Nicolas. “Évaluation de la génotoxicité des contaminants environnementaux, production de lignées bio-senseurs et mesure de l'activité enzymatique du cytochrome P450 2E1 dans les cellules d'hépatome humain HepaRG : Evaluation of genotoxicity of environmental contaminants,production of bio-sensor cell lines and measurment of CYP2E1 enzymatic activity.” 2015. Web. 17 Apr 2021.

Vancouver:

Quesnot N. Évaluation de la génotoxicité des contaminants environnementaux, production de lignées bio-senseurs et mesure de l'activité enzymatique du cytochrome P450 2E1 dans les cellules d'hépatome humain HepaRG : Evaluation of genotoxicity of environmental contaminants,production of bio-sensor cell lines and measurment of CYP2E1 enzymatic activity. [Internet] [Doctoral dissertation]. Rennes 1; 2015. [cited 2021 Apr 17]. Available from: http://www.theses.fr/2015REN1B005.

Council of Science Editors:

Quesnot N. Évaluation de la génotoxicité des contaminants environnementaux, production de lignées bio-senseurs et mesure de l'activité enzymatique du cytochrome P450 2E1 dans les cellules d'hépatome humain HepaRG : Evaluation of genotoxicity of environmental contaminants,production of bio-sensor cell lines and measurment of CYP2E1 enzymatic activity. [Doctoral Dissertation]. Rennes 1; 2015. Available from: http://www.theses.fr/2015REN1B005


University of Bradford

27. Presa, Daniella F. S. Investigation of cytochrome p450 isoforms 1A1, 1B1 and 2W1 as targets for therapeutic intervention in head and neck cancer : probing CYP1A1, 1B1 and 2W1 activity with duocarmycin bioprecursors.

Degree: PhD, 2018, University of Bradford

Subjects/Keywords: Cytochrome P450 (CYP); CYP1A1; CYP1B1; CYP2W1; Head and Neck Cancer (HNC); Duocarmycin; Prodrug; Bioprecursor; DNA damage; Therapeutic intervention

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APA (6th Edition):

Presa, D. F. S. (2018). Investigation of cytochrome p450 isoforms 1A1, 1B1 and 2W1 as targets for therapeutic intervention in head and neck cancer : probing CYP1A1, 1B1 and 2W1 activity with duocarmycin bioprecursors. (Doctoral Dissertation). University of Bradford. Retrieved from http://hdl.handle.net/10454/18171

Chicago Manual of Style (16th Edition):

Presa, Daniella F S. “Investigation of cytochrome p450 isoforms 1A1, 1B1 and 2W1 as targets for therapeutic intervention in head and neck cancer : probing CYP1A1, 1B1 and 2W1 activity with duocarmycin bioprecursors.” 2018. Doctoral Dissertation, University of Bradford. Accessed April 17, 2021. http://hdl.handle.net/10454/18171.

MLA Handbook (7th Edition):

Presa, Daniella F S. “Investigation of cytochrome p450 isoforms 1A1, 1B1 and 2W1 as targets for therapeutic intervention in head and neck cancer : probing CYP1A1, 1B1 and 2W1 activity with duocarmycin bioprecursors.” 2018. Web. 17 Apr 2021.

Vancouver:

Presa DFS. Investigation of cytochrome p450 isoforms 1A1, 1B1 and 2W1 as targets for therapeutic intervention in head and neck cancer : probing CYP1A1, 1B1 and 2W1 activity with duocarmycin bioprecursors. [Internet] [Doctoral dissertation]. University of Bradford; 2018. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/10454/18171.

Council of Science Editors:

Presa DFS. Investigation of cytochrome p450 isoforms 1A1, 1B1 and 2W1 as targets for therapeutic intervention in head and neck cancer : probing CYP1A1, 1B1 and 2W1 activity with duocarmycin bioprecursors. [Doctoral Dissertation]. University of Bradford; 2018. Available from: http://hdl.handle.net/10454/18171


University of Alberta

28. Tse, Mandy M.Y. The role of cytochrome P450 and the protective effect of EETs against isoproterenol-induced cellular hypertrophy in rat H9c2 cell line.

Degree: MS, Faculty of Pharmacy and Pharmaceutical Sciences, 2013, University of Alberta

Cytochrome P450 (CYP) enzymes have been identified in the heart and their levels have been reported to be altered during cardiac hypertrophy and heart failure.… (more)

Subjects/Keywords: hypertrophy; H9c2 cell; cytochrome P450; EETs

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APA (6th Edition):

Tse, M. M. Y. (2013). The role of cytochrome P450 and the protective effect of EETs against isoproterenol-induced cellular hypertrophy in rat H9c2 cell line. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/3t945r43f

Chicago Manual of Style (16th Edition):

Tse, Mandy M Y. “The role of cytochrome P450 and the protective effect of EETs against isoproterenol-induced cellular hypertrophy in rat H9c2 cell line.” 2013. Masters Thesis, University of Alberta. Accessed April 17, 2021. https://era.library.ualberta.ca/files/3t945r43f.

MLA Handbook (7th Edition):

Tse, Mandy M Y. “The role of cytochrome P450 and the protective effect of EETs against isoproterenol-induced cellular hypertrophy in rat H9c2 cell line.” 2013. Web. 17 Apr 2021.

Vancouver:

Tse MMY. The role of cytochrome P450 and the protective effect of EETs against isoproterenol-induced cellular hypertrophy in rat H9c2 cell line. [Internet] [Masters thesis]. University of Alberta; 2013. [cited 2021 Apr 17]. Available from: https://era.library.ualberta.ca/files/3t945r43f.

Council of Science Editors:

Tse MMY. The role of cytochrome P450 and the protective effect of EETs against isoproterenol-induced cellular hypertrophy in rat H9c2 cell line. [Masters Thesis]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/3t945r43f

29. Nisbar, Nur Dayana binti. Characterisation of orphan cytochrome P450s from Mycobacterium tuberculosis H37Rv.

Degree: 2018, University of Manchester

 Tuberculosis is a disease that kills more people every year than any other infectious disease and is caused by the human pathogen, Mycobacterium tuberculosis (Mtb).… (more)

Subjects/Keywords: Tuberculosis; Cytochrome P450; Fragment-based drug discovery

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

APA (6th Edition):

Nisbar, N. D. b. (2018). Characterisation of orphan cytochrome P450s from Mycobacterium tuberculosis H37Rv. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313431

Chicago Manual of Style (16th Edition):

Nisbar, Nur Dayana binti. “Characterisation of orphan cytochrome P450s from Mycobacterium tuberculosis H37Rv.” 2018. Doctoral Dissertation, University of Manchester. Accessed April 17, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313431.

MLA Handbook (7th Edition):

Nisbar, Nur Dayana binti. “Characterisation of orphan cytochrome P450s from Mycobacterium tuberculosis H37Rv.” 2018. Web. 17 Apr 2021.

Vancouver:

Nisbar NDb. Characterisation of orphan cytochrome P450s from Mycobacterium tuberculosis H37Rv. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2021 Apr 17]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313431.

Council of Science Editors:

Nisbar NDb. Characterisation of orphan cytochrome P450s from Mycobacterium tuberculosis H37Rv. [Doctoral Dissertation]. University of Manchester; 2018. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313431


Vanderbilt University

30. Albertolle, Matthew Edward. SULFENYLATION OF CYTOCHROMES P450 IN RESPONSE TO REDOX ALTERATION.

Degree: PhD, Biochemistry, 2019, Vanderbilt University

 Mammalian cytochrome P450 (P450) enzymes catalyze complex reactions involved in the biosynthesis of endogenous metabolites such as steroids, vitamins, and hormones. Additionally, several enzymes in… (more)

Subjects/Keywords: Cytochrome P450; Redox; Enzymology; Proteomics; Sulfenic Acid

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

APA (6th Edition):

Albertolle, M. E. (2019). SULFENYLATION OF CYTOCHROMES P450 IN RESPONSE TO REDOX ALTERATION. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10450

Chicago Manual of Style (16th Edition):

Albertolle, Matthew Edward. “SULFENYLATION OF CYTOCHROMES P450 IN RESPONSE TO REDOX ALTERATION.” 2019. Doctoral Dissertation, Vanderbilt University. Accessed April 17, 2021. http://hdl.handle.net/1803/10450.

MLA Handbook (7th Edition):

Albertolle, Matthew Edward. “SULFENYLATION OF CYTOCHROMES P450 IN RESPONSE TO REDOX ALTERATION.” 2019. Web. 17 Apr 2021.

Vancouver:

Albertolle ME. SULFENYLATION OF CYTOCHROMES P450 IN RESPONSE TO REDOX ALTERATION. [Internet] [Doctoral dissertation]. Vanderbilt University; 2019. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/1803/10450.

Council of Science Editors:

Albertolle ME. SULFENYLATION OF CYTOCHROMES P450 IN RESPONSE TO REDOX ALTERATION. [Doctoral Dissertation]. Vanderbilt University; 2019. Available from: http://hdl.handle.net/1803/10450

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