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You searched for subject:(P450). Showing records 1 – 30 of 589 total matches.

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1. 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 March 06, 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. 06 Mar 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 Mar 06]. 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/


University of Manchester

2. 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 March 06, 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. 06 Mar 2021.

Vancouver:

Porro CS. Quantum mechanical/molecular mechanics studies of Cytochrome P450BM3. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2021 Mar 06]. 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


Brandeis University

3. Lloyd, Hannah. Searching for novel terpene-specific cytochromes P450 in soil bacteria.

Degree: 2020, Brandeis University

 Cytochromes P450 are powerful enzymes capable of catalyzing oxidation of unactivated carbon-hydrogen bonds at physiological temperatures and pH. They are ubiquitous to life, yet the… (more)

Subjects/Keywords: Cytochromes P450; Terpenes

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APA (6th Edition):

Lloyd, H. (2020). Searching for novel terpene-specific cytochromes P450 in soil bacteria. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/37519

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):

Lloyd, Hannah. “Searching for novel terpene-specific cytochromes P450 in soil bacteria.” 2020. Thesis, Brandeis University. Accessed March 06, 2021. http://hdl.handle.net/10192/37519.

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

MLA Handbook (7th Edition):

Lloyd, Hannah. “Searching for novel terpene-specific cytochromes P450 in soil bacteria.” 2020. Web. 06 Mar 2021.

Vancouver:

Lloyd H. Searching for novel terpene-specific cytochromes P450 in soil bacteria. [Internet] [Thesis]. Brandeis University; 2020. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/10192/37519.

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

Council of Science Editors:

Lloyd H. Searching for novel terpene-specific cytochromes P450 in soil bacteria. [Thesis]. Brandeis University; 2020. Available from: http://hdl.handle.net/10192/37519

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


University of Illinois – Urbana-Champaign

4. Gregory, Michael Carlton. Understanding the mechanism of androgen biosynthesis.

Degree: PhD, Biochemistry, 2016, University of Illinois – Urbana-Champaign

 Cytochrome P45017A1 (CYP17A1) is a multifunctional steroidogenic enzyme responsible for the 17-hydroxylation of pregnenolone and progesterone as well as the subsequent 17,20 carbon-carbon bond scission… (more)

Subjects/Keywords: CYP17A1; Nanodisc; P450

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APA (6th Edition):

Gregory, M. C. (2016). Understanding the mechanism of androgen biosynthesis. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95533

Chicago Manual of Style (16th Edition):

Gregory, Michael Carlton. “Understanding the mechanism of androgen biosynthesis.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed March 06, 2021. http://hdl.handle.net/2142/95533.

MLA Handbook (7th Edition):

Gregory, Michael Carlton. “Understanding the mechanism of androgen biosynthesis.” 2016. Web. 06 Mar 2021.

Vancouver:

Gregory MC. Understanding the mechanism of androgen biosynthesis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/2142/95533.

Council of Science Editors:

Gregory MC. Understanding the mechanism of androgen biosynthesis. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95533


University of Utah

5. 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 March 06, 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. 06 Mar 2021.

Vancouver:

Moore CD. Dehydrogenation of Raloxifene by Cytochrome P450 3A4. [Internet] [Doctoral dissertation]. University of Utah; 2010. [cited 2021 Mar 06]. 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

6. 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 March 06, 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. 06 Mar 2021.

Vancouver:

Bardowell S. The Role Of Vitamin E Hydroxylases In Vitamin E Metabolism And Status. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2021 Mar 06]. 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 Adelaide

7. Lee, Joel Hoong Zhang. Harnessing P450 enzymes as biocatalysts for selective C-H bond hydroxylation.

Degree: 2018, University of Adelaide

 The cytochrome P450 enzyme, CYP101B1 from Novosphingobhium aromaticivorans can catalyse the highly efficient and regioselective oxidation of norisoprenoids. However, it has lower affinity towards hydrophobic… (more)

Subjects/Keywords: P450; biocatalysis; food; fragrance; hydroxylation

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APA (6th Edition):

Lee, J. H. Z. (2018). Harnessing P450 enzymes as biocatalysts for selective C-H bond hydroxylation. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/118161

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):

Lee, Joel Hoong Zhang. “Harnessing P450 enzymes as biocatalysts for selective C-H bond hydroxylation.” 2018. Thesis, University of Adelaide. Accessed March 06, 2021. http://hdl.handle.net/2440/118161.

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

MLA Handbook (7th Edition):

Lee, Joel Hoong Zhang. “Harnessing P450 enzymes as biocatalysts for selective C-H bond hydroxylation.” 2018. Web. 06 Mar 2021.

Vancouver:

Lee JHZ. Harnessing P450 enzymes as biocatalysts for selective C-H bond hydroxylation. [Internet] [Thesis]. University of Adelaide; 2018. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/2440/118161.

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

Council of Science Editors:

Lee JHZ. Harnessing P450 enzymes as biocatalysts for selective C-H bond hydroxylation. [Thesis]. University of Adelaide; 2018. Available from: http://hdl.handle.net/2440/118161

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


University of Guelph

8. 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 March 06, 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. 06 Mar 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 Mar 06]. 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

9. Baker, George. The characterisation of the flavocytochrome P450-CPR fusion enzymes CYP505A30 from Myceliophthora thermophila and CYP102A1 from Bacillus megaterium.

Degree: PhD, 2016, University of Manchester

 High catalytic activity and a broad substrate range are characteristic of P450 fusion enzymes of the CYP102A class. P450 BM3 (CYP102A1, BM3) is a paradigm… (more)

Subjects/Keywords: 572; fusion P450; BM3; thermophile

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APA (6th Edition):

Baker, G. (2016). The characterisation of the flavocytochrome P450-CPR fusion enzymes CYP505A30 from Myceliophthora thermophila and CYP102A1 from Bacillus megaterium. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/the-characterisation-of-the-flavocytochrome-p450cpr-fusion-enzymes-cyp505a30-from-myceliophthora-thermophila-and-cyp102a1-from-bacillus-megaterium(f064fb08-300f-4d09-a03a-f00017c4ba68).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.684802

Chicago Manual of Style (16th Edition):

Baker, George. “The characterisation of the flavocytochrome P450-CPR fusion enzymes CYP505A30 from Myceliophthora thermophila and CYP102A1 from Bacillus megaterium.” 2016. Doctoral Dissertation, University of Manchester. Accessed March 06, 2021. https://www.research.manchester.ac.uk/portal/en/theses/the-characterisation-of-the-flavocytochrome-p450cpr-fusion-enzymes-cyp505a30-from-myceliophthora-thermophila-and-cyp102a1-from-bacillus-megaterium(f064fb08-300f-4d09-a03a-f00017c4ba68).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.684802.

MLA Handbook (7th Edition):

Baker, George. “The characterisation of the flavocytochrome P450-CPR fusion enzymes CYP505A30 from Myceliophthora thermophila and CYP102A1 from Bacillus megaterium.” 2016. Web. 06 Mar 2021.

Vancouver:

Baker G. The characterisation of the flavocytochrome P450-CPR fusion enzymes CYP505A30 from Myceliophthora thermophila and CYP102A1 from Bacillus megaterium. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2021 Mar 06]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-characterisation-of-the-flavocytochrome-p450cpr-fusion-enzymes-cyp505a30-from-myceliophthora-thermophila-and-cyp102a1-from-bacillus-megaterium(f064fb08-300f-4d09-a03a-f00017c4ba68).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.684802.

Council of Science Editors:

Baker G. The characterisation of the flavocytochrome P450-CPR fusion enzymes CYP505A30 from Myceliophthora thermophila and CYP102A1 from Bacillus megaterium. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-characterisation-of-the-flavocytochrome-p450cpr-fusion-enzymes-cyp505a30-from-myceliophthora-thermophila-and-cyp102a1-from-bacillus-megaterium(f064fb08-300f-4d09-a03a-f00017c4ba68).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.684802


University of Manchester

10. 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 March 06, 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. 06 Mar 2021.

Vancouver:

Matthews S. Characterisation and Engineering of Alkene Producing P450 Peroxygenases for Bioenergy Applications. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2021 Mar 06]. 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 Manchester

11. Baker, George. The characterisation of the flavocytochrome P450-CPR fusion enzymes CYP505A30 from Myceliophthora thermophila and CYP102A1 from Bacillus megaterium.

Degree: 2016, University of Manchester

 High catalytic activity and a broad substrate range are characteristic of P450 fusion enzymes of the CYP102A class. P450 BM3 (CYP102A1, BM3) is a paradigm… (more)

Subjects/Keywords: fusion P450; BM3; thermophile

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APA (6th Edition):

Baker, G. (2016). The characterisation of the flavocytochrome P450-CPR fusion enzymes CYP505A30 from Myceliophthora thermophila and CYP102A1 from Bacillus megaterium. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:297035

Chicago Manual of Style (16th Edition):

Baker, George. “The characterisation of the flavocytochrome P450-CPR fusion enzymes CYP505A30 from Myceliophthora thermophila and CYP102A1 from Bacillus megaterium.” 2016. Doctoral Dissertation, University of Manchester. Accessed March 06, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:297035.

MLA Handbook (7th Edition):

Baker, George. “The characterisation of the flavocytochrome P450-CPR fusion enzymes CYP505A30 from Myceliophthora thermophila and CYP102A1 from Bacillus megaterium.” 2016. Web. 06 Mar 2021.

Vancouver:

Baker G. The characterisation of the flavocytochrome P450-CPR fusion enzymes CYP505A30 from Myceliophthora thermophila and CYP102A1 from Bacillus megaterium. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2021 Mar 06]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:297035.

Council of Science Editors:

Baker G. The characterisation of the flavocytochrome P450-CPR fusion enzymes CYP505A30 from Myceliophthora thermophila and CYP102A1 from Bacillus megaterium. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:297035


University of Texas – Austin

12. 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 March 06, 2021. http://hdl.handle.net/2152/46526.

MLA Handbook (7th Edition):

Sunnadeniya, Rasika Mayanthi. “Identification and functional analysis of betalain pathway genes.” 2014. Web. 06 Mar 2021.

Vancouver:

Sunnadeniya RM. Identification and functional analysis of betalain pathway genes. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2021 Mar 06]. 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


Vanderbilt University

13. Gonzalez, Eric. The Kinetic and Chemical Mechanisms of Human Cytochrome P450 17A1.

Degree: PhD, Biochemistry, 2017, Vanderbilt University

 Human cytochrome P450 (P450) 17A1 is an essential enzyme in the steroid biosynthesis pathway that mediates a critical branch point which leads to either glucocorticoid… (more)

Subjects/Keywords: enzyme kinetics; prostate cancer; P450 17A1; cytochrome P450

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APA (6th Edition):

Gonzalez, E. (2017). The Kinetic and Chemical Mechanisms of Human Cytochrome P450 17A1. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12107

Chicago Manual of Style (16th Edition):

Gonzalez, Eric. “The Kinetic and Chemical Mechanisms of Human Cytochrome P450 17A1.” 2017. Doctoral Dissertation, Vanderbilt University. Accessed March 06, 2021. http://hdl.handle.net/1803/12107.

MLA Handbook (7th Edition):

Gonzalez, Eric. “The Kinetic and Chemical Mechanisms of Human Cytochrome P450 17A1.” 2017. Web. 06 Mar 2021.

Vancouver:

Gonzalez E. The Kinetic and Chemical Mechanisms of Human Cytochrome P450 17A1. [Internet] [Doctoral dissertation]. Vanderbilt University; 2017. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1803/12107.

Council of Science Editors:

Gonzalez E. The Kinetic and Chemical Mechanisms of Human Cytochrome P450 17A1. [Doctoral Dissertation]. Vanderbilt University; 2017. Available from: http://hdl.handle.net/1803/12107

14. 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 March 06, 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. 06 Mar 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 Mar 06]. 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 Manchester

15. Povsic, Manca. Rational redesign of cytochrome P450 BM3 (CYP102A1) towards industrially relevant drug metabolites.

Degree: 2015, University of Manchester

 The University of ManchesterManca PovsicRational redesign of cytochrome P450 BM3 (CYP102A1) towards industrially relevant drug metabolitesSeptember 2015Human drug metabolites are frequently biologically active, with many… (more)

Subjects/Keywords: cytochrome P450; P450 BM3; drug metabolites; protein engineering; biotechnology

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

APA (6th Edition):

Povsic, M. (2015). Rational redesign of cytochrome P450 BM3 (CYP102A1) towards industrially relevant drug metabolites. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:293526

Chicago Manual of Style (16th Edition):

Povsic, Manca. “Rational redesign of cytochrome P450 BM3 (CYP102A1) towards industrially relevant drug metabolites.” 2015. Doctoral Dissertation, University of Manchester. Accessed March 06, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:293526.

MLA Handbook (7th Edition):

Povsic, Manca. “Rational redesign of cytochrome P450 BM3 (CYP102A1) towards industrially relevant drug metabolites.” 2015. Web. 06 Mar 2021.

Vancouver:

Povsic M. Rational redesign of cytochrome P450 BM3 (CYP102A1) towards industrially relevant drug metabolites. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2021 Mar 06]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:293526.

Council of Science Editors:

Povsic M. Rational redesign of cytochrome P450 BM3 (CYP102A1) towards industrially relevant drug metabolites. [Doctoral Dissertation]. University of Manchester; 2015. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:293526


University of Manchester

16. Povsic, Manca. Rational redesign of cytochrome P450 BM3 (CYP102A1) towards industrially relevant drug metabolites.

Degree: PhD, 2016, University of Manchester

 Human drug metabolites are frequently biologically active, with many implications for human health. Pharmaceutical companies have become increasingly aware of the need to identify and… (more)

Subjects/Keywords: 615.1; cytochrome P450; P450 BM3; drug metabolites; protein engineering; biotechnology

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

APA (6th Edition):

Povsic, M. (2016). Rational redesign of cytochrome P450 BM3 (CYP102A1) towards industrially relevant drug metabolites. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/rational-redesign-of-cytochrome-p450-bm3-cyp102a1-towards-industrially-relevant-drug-metabolites(1e9b4e44-0211-4ffc-8684-7db1c9a21791).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764467

Chicago Manual of Style (16th Edition):

Povsic, Manca. “Rational redesign of cytochrome P450 BM3 (CYP102A1) towards industrially relevant drug metabolites.” 2016. Doctoral Dissertation, University of Manchester. Accessed March 06, 2021. https://www.research.manchester.ac.uk/portal/en/theses/rational-redesign-of-cytochrome-p450-bm3-cyp102a1-towards-industrially-relevant-drug-metabolites(1e9b4e44-0211-4ffc-8684-7db1c9a21791).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764467.

MLA Handbook (7th Edition):

Povsic, Manca. “Rational redesign of cytochrome P450 BM3 (CYP102A1) towards industrially relevant drug metabolites.” 2016. Web. 06 Mar 2021.

Vancouver:

Povsic M. Rational redesign of cytochrome P450 BM3 (CYP102A1) towards industrially relevant drug metabolites. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2021 Mar 06]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/rational-redesign-of-cytochrome-p450-bm3-cyp102a1-towards-industrially-relevant-drug-metabolites(1e9b4e44-0211-4ffc-8684-7db1c9a21791).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764467.

Council of Science Editors:

Povsic M. Rational redesign of cytochrome P450 BM3 (CYP102A1) towards industrially relevant drug metabolites. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/rational-redesign-of-cytochrome-p450-bm3-cyp102a1-towards-industrially-relevant-drug-metabolites(1e9b4e44-0211-4ffc-8684-7db1c9a21791).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764467


University of Alberta

17. 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 March 06, 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. 06 Mar 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 Mar 06]. 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

18. 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 March 06, 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. 06 Mar 2021.

Vancouver:

Nisbar NDb. Characterisation of orphan cytochrome P450s from Mycobacterium tuberculosis H37Rv. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2021 Mar 06]. 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

19. 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 March 06, 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. 06 Mar 2021.

Vancouver:

Albertolle ME. SULFENYLATION OF CYTOCHROMES P450 IN RESPONSE TO REDOX ALTERATION. [Internet] [Doctoral dissertation]. Vanderbilt University; 2019. [cited 2021 Mar 06]. 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

20. Venkatachalam, Arunachalam. ICP-MS based analytical screening of phosphorylated and labelled proteins.

Degree: 2009, Technische Universität Dortmund

Die induktiv gekoppelte Plasma-Massenspektrometrie (ICP-MS) wird bereits für viele biologische Anwendungen eingesetzt. Diese Methode liefert qualitative und quantitative elementspezifische Informationen, die zur Bestimmung des Zustands… (more)

Subjects/Keywords: Cytochromes; LA-ICP_MS; P450; Phosphorylation; 660

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APA (6th Edition):

Venkatachalam, Arunachalam. (2009). ICP-MS based analytical screening of phosphorylated and labelled proteins. (Thesis). Technische Universität Dortmund. Retrieved from http://hdl.handle.net/2003/26433

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

Chicago Manual of Style (16th Edition):

Venkatachalam, Arunachalam. “ICP-MS based analytical screening of phosphorylated and labelled proteins.” 2009. Thesis, Technische Universität Dortmund. Accessed March 06, 2021. http://hdl.handle.net/2003/26433.

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

MLA Handbook (7th Edition):

Venkatachalam, Arunachalam. “ICP-MS based analytical screening of phosphorylated and labelled proteins.” 2009. Web. 06 Mar 2021.

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

Vancouver:

Venkatachalam, Arunachalam. ICP-MS based analytical screening of phosphorylated and labelled proteins. [Internet] [Thesis]. Technische Universität Dortmund; 2009. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/2003/26433.

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

Council of Science Editors:

Venkatachalam, Arunachalam. ICP-MS based analytical screening of phosphorylated and labelled proteins. [Thesis]. Technische Universität Dortmund; 2009. Available from: http://hdl.handle.net/2003/26433

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


Penn State University

21. Keller, Rebecca Lynn. Structure and Dynamics of C-H-Bond-Cleaving High-Valent Iron Intermediates.

Degree: 2012, Penn State University

 C-H bond cleavage is one of the primary tenets of the chemical world. Industry has long searched for more efficient commercial processes to functionalize C-H… (more)

Subjects/Keywords: C-H activation; TauD; Bleomycin; P450

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APA (6th Edition):

Keller, R. L. (2012). Structure and Dynamics of C-H-Bond-Cleaving High-Valent Iron Intermediates. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/14215

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):

Keller, Rebecca Lynn. “Structure and Dynamics of C-H-Bond-Cleaving High-Valent Iron Intermediates.” 2012. Thesis, Penn State University. Accessed March 06, 2021. https://submit-etda.libraries.psu.edu/catalog/14215.

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

MLA Handbook (7th Edition):

Keller, Rebecca Lynn. “Structure and Dynamics of C-H-Bond-Cleaving High-Valent Iron Intermediates.” 2012. Web. 06 Mar 2021.

Vancouver:

Keller RL. Structure and Dynamics of C-H-Bond-Cleaving High-Valent Iron Intermediates. [Internet] [Thesis]. Penn State University; 2012. [cited 2021 Mar 06]. Available from: https://submit-etda.libraries.psu.edu/catalog/14215.

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

Council of Science Editors:

Keller RL. Structure and Dynamics of C-H-Bond-Cleaving High-Valent Iron Intermediates. [Thesis]. Penn State University; 2012. Available from: https://submit-etda.libraries.psu.edu/catalog/14215

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


Penn State University

22. Yosca, Timothy Howard. Understanding C-H Bond Activation in Heme Proteins: The Importance of the Ferryl pKa.

Degree: 2012, Penn State University

 The major focus of the Green group involves the study of C-H bond activation by heme proteins and the elucidation of the factors giving rise… (more)

Subjects/Keywords: cytochrome p450; compound II; ferryl pKa

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APA (6th Edition):

Yosca, T. H. (2012). Understanding C-H Bond Activation in Heme Proteins: The Importance of the Ferryl pKa. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/16041

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):

Yosca, Timothy Howard. “Understanding C-H Bond Activation in Heme Proteins: The Importance of the Ferryl pKa.” 2012. Thesis, Penn State University. Accessed March 06, 2021. https://submit-etda.libraries.psu.edu/catalog/16041.

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

MLA Handbook (7th Edition):

Yosca, Timothy Howard. “Understanding C-H Bond Activation in Heme Proteins: The Importance of the Ferryl pKa.” 2012. Web. 06 Mar 2021.

Vancouver:

Yosca TH. Understanding C-H Bond Activation in Heme Proteins: The Importance of the Ferryl pKa. [Internet] [Thesis]. Penn State University; 2012. [cited 2021 Mar 06]. Available from: https://submit-etda.libraries.psu.edu/catalog/16041.

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

Council of Science Editors:

Yosca TH. Understanding C-H Bond Activation in Heme Proteins: The Importance of the Ferryl pKa. [Thesis]. Penn State University; 2012. Available from: https://submit-etda.libraries.psu.edu/catalog/16041

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


University of Saskatchewan

23. Boyd, Erin Margaret Rose. Phase I and II enzyme induction and inhibition by secoisolariciresinol diglucoside and it's aglycone.

Degree: 2007, University of Saskatchewan

 The flaxseed lignan, secoisolariciresinol diglucoside (SDG), and its aglycone, secoisolariciresinol (SECO), have demonstrated benefits in the treatment and/or prevention of cancer, diabetes and cardiovascular disease.… (more)

Subjects/Keywords: Cytochrome P450; Flaxseed

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APA (6th Edition):

Boyd, E. M. R. (2007). Phase I and II enzyme induction and inhibition by secoisolariciresinol diglucoside and it's aglycone. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/etd-04262007-161734

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):

Boyd, Erin Margaret Rose. “Phase I and II enzyme induction and inhibition by secoisolariciresinol diglucoside and it's aglycone.” 2007. Thesis, University of Saskatchewan. Accessed March 06, 2021. http://hdl.handle.net/10388/etd-04262007-161734.

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

MLA Handbook (7th Edition):

Boyd, Erin Margaret Rose. “Phase I and II enzyme induction and inhibition by secoisolariciresinol diglucoside and it's aglycone.” 2007. Web. 06 Mar 2021.

Vancouver:

Boyd EMR. Phase I and II enzyme induction and inhibition by secoisolariciresinol diglucoside and it's aglycone. [Internet] [Thesis]. University of Saskatchewan; 2007. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/10388/etd-04262007-161734.

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

Council of Science Editors:

Boyd EMR. Phase I and II enzyme induction and inhibition by secoisolariciresinol diglucoside and it's aglycone. [Thesis]. University of Saskatchewan; 2007. Available from: http://hdl.handle.net/10388/etd-04262007-161734

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

24. Cunha, Andrea Teixeira da. Análise populacional e funcional dos polimorfismos genéticos CYP2D6*4 e CYP2C19*17 do citocromo P450 e C3435T do gene MDR1.

Degree: 2013, RCAAP

 A variabilidade da resposta aos fármacos deve-se, em grande parte, a fatores genéticos. Polimorfismos em genes que codificam enzimas metabolizadoras de xenobióticos, como as enzimas… (more)

Subjects/Keywords: Enzimas CYP2D6 e CYP2C19; Citocromo P450 (CYP450)

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APA (6th Edition):

Cunha, A. T. d. (2013). Análise populacional e funcional dos polimorfismos genéticos CYP2D6*4 e CYP2C19*17 do citocromo P450 e C3435T do gene MDR1. (Thesis). RCAAP. Retrieved from https://www.rcaap.pt/detail.jsp?id=oai:repositorio.cespu.pt:20.500.11816/315

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):

Cunha, Andrea Teixeira da. “Análise populacional e funcional dos polimorfismos genéticos CYP2D6*4 e CYP2C19*17 do citocromo P450 e C3435T do gene MDR1.” 2013. Thesis, RCAAP. Accessed March 06, 2021. https://www.rcaap.pt/detail.jsp?id=oai:repositorio.cespu.pt:20.500.11816/315.

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

MLA Handbook (7th Edition):

Cunha, Andrea Teixeira da. “Análise populacional e funcional dos polimorfismos genéticos CYP2D6*4 e CYP2C19*17 do citocromo P450 e C3435T do gene MDR1.” 2013. Web. 06 Mar 2021.

Vancouver:

Cunha ATd. Análise populacional e funcional dos polimorfismos genéticos CYP2D6*4 e CYP2C19*17 do citocromo P450 e C3435T do gene MDR1. [Internet] [Thesis]. RCAAP; 2013. [cited 2021 Mar 06]. Available from: https://www.rcaap.pt/detail.jsp?id=oai:repositorio.cespu.pt:20.500.11816/315.

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

Council of Science Editors:

Cunha ATd. Análise populacional e funcional dos polimorfismos genéticos CYP2D6*4 e CYP2C19*17 do citocromo P450 e C3435T do gene MDR1. [Thesis]. RCAAP; 2013. Available from: https://www.rcaap.pt/detail.jsp?id=oai:repositorio.cespu.pt:20.500.11816/315

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


University of Adelaide

25. Child, Stella Agnes. Deciphering electron transfer and cytochrome P450 activity in Mycobacterium marinum.

Degree: 2018, University of Adelaide

 Cytochrome P450s are haem-monooxygenase enzymes, responsible for the catalytic hydroxylation of a large variety of organic molecules. The bacterium Mycobacterium marinum, has a larger genome… (more)

Subjects/Keywords: Electron transfer; cytochrome P450; mycobacteria; biocatalysis

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APA (6th Edition):

Child, S. A. (2018). Deciphering electron transfer and cytochrome P450 activity in Mycobacterium marinum. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/118202

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):

Child, Stella Agnes. “Deciphering electron transfer and cytochrome P450 activity in Mycobacterium marinum.” 2018. Thesis, University of Adelaide. Accessed March 06, 2021. http://hdl.handle.net/2440/118202.

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

MLA Handbook (7th Edition):

Child, Stella Agnes. “Deciphering electron transfer and cytochrome P450 activity in Mycobacterium marinum.” 2018. Web. 06 Mar 2021.

Vancouver:

Child SA. Deciphering electron transfer and cytochrome P450 activity in Mycobacterium marinum. [Internet] [Thesis]. University of Adelaide; 2018. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/2440/118202.

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

Council of Science Editors:

Child SA. Deciphering electron transfer and cytochrome P450 activity in Mycobacterium marinum. [Thesis]. University of Adelaide; 2018. Available from: http://hdl.handle.net/2440/118202

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

26. António, Mara Guedes. Interações do tabagismo com a terapêutica farmacológica.

Degree: 2013, RCAAP

Dissertação para obtenção do grau de Mestre no Instituto Superior de Ciências da Saúde Egas Moniz

O cigarro é constituído por inúmeras substâncias, nomeadamente a… (more)

Subjects/Keywords: Citocromo P450; Tabaco; Interações farmacocinéticas; Interações farmacodinâmicas

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

APA (6th Edition):

António, M. G. (2013). Interações do tabagismo com a terapêutica farmacológica. (Thesis). RCAAP. Retrieved from https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/14164

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):

António, Mara Guedes. “Interações do tabagismo com a terapêutica farmacológica.” 2013. Thesis, RCAAP. Accessed March 06, 2021. https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/14164.

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

MLA Handbook (7th Edition):

António, Mara Guedes. “Interações do tabagismo com a terapêutica farmacológica.” 2013. Web. 06 Mar 2021.

Vancouver:

António MG. Interações do tabagismo com a terapêutica farmacológica. [Internet] [Thesis]. RCAAP; 2013. [cited 2021 Mar 06]. Available from: https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/14164.

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

Council of Science Editors:

António MG. Interações do tabagismo com a terapêutica farmacológica. [Thesis]. RCAAP; 2013. Available from: https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/14164

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


University of Manchester

27. Cantu Reinhard, Fabian Gilberto. A Computational Chemistry Approach to Cytochrome P450 Metabolism.

Degree: 2018, University of Manchester

 Drugs and other xenobiotic compounds exhibit different transformations upon entering the human body, most often starting with an oxidative reaction involving P450 enzymes. Hence, the… (more)

Subjects/Keywords: DFT; P450; Computational Chemistry; Drug Metabolism

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

APA (6th Edition):

Cantu Reinhard, F. G. (2018). A Computational Chemistry Approach to Cytochrome P450 Metabolism. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:317301

Chicago Manual of Style (16th Edition):

Cantu Reinhard, Fabian Gilberto. “A Computational Chemistry Approach to Cytochrome P450 Metabolism.” 2018. Doctoral Dissertation, University of Manchester. Accessed March 06, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:317301.

MLA Handbook (7th Edition):

Cantu Reinhard, Fabian Gilberto. “A Computational Chemistry Approach to Cytochrome P450 Metabolism.” 2018. Web. 06 Mar 2021.

Vancouver:

Cantu Reinhard FG. A Computational Chemistry Approach to Cytochrome P450 Metabolism. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2021 Mar 06]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:317301.

Council of Science Editors:

Cantu Reinhard FG. A Computational Chemistry Approach to Cytochrome P450 Metabolism. [Doctoral Dissertation]. University of Manchester; 2018. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:317301


University of Toronto

28. Tsai, Chieh. The Effects of Uremic Serum from Hemodialysis Patients on Hepatic Cyochrome P450 and VKORC1 Gene Expression in Primary Human Hepatocytes.

Degree: 2017, University of Toronto

Warfarin is frequently prescribed to patients with atrial fibrillation (AF) who are on hemodialysis (HD) for stroke prevention regardless of conflicting evidence showing unclear benefits… (more)

Subjects/Keywords: Cytochrome P450; Hemodialysis; VKORC1; Warfarin; 0572

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

APA (6th Edition):

Tsai, C. (2017). The Effects of Uremic Serum from Hemodialysis Patients on Hepatic Cyochrome P450 and VKORC1 Gene Expression in Primary Human Hepatocytes. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/77912

Chicago Manual of Style (16th Edition):

Tsai, Chieh. “The Effects of Uremic Serum from Hemodialysis Patients on Hepatic Cyochrome P450 and VKORC1 Gene Expression in Primary Human Hepatocytes.” 2017. Masters Thesis, University of Toronto. Accessed March 06, 2021. http://hdl.handle.net/1807/77912.

MLA Handbook (7th Edition):

Tsai, Chieh. “The Effects of Uremic Serum from Hemodialysis Patients on Hepatic Cyochrome P450 and VKORC1 Gene Expression in Primary Human Hepatocytes.” 2017. Web. 06 Mar 2021.

Vancouver:

Tsai C. The Effects of Uremic Serum from Hemodialysis Patients on Hepatic Cyochrome P450 and VKORC1 Gene Expression in Primary Human Hepatocytes. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1807/77912.

Council of Science Editors:

Tsai C. The Effects of Uremic Serum from Hemodialysis Patients on Hepatic Cyochrome P450 and VKORC1 Gene Expression in Primary Human Hepatocytes. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/77912


University of Illinois – Chicago

29. 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 · 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/10027/21572

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 March 06, 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. 06 Mar 2021.

Vancouver:

Zhang S. Transcriptional Regulation of CYP3A4 and CYP2D6 by Small Heterodimer Partner. [Internet] [Thesis]. University of Illinois – Chicago; 2016. [cited 2021 Mar 06]. 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

30. 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/10027/21629

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 March 06, 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. 06 Mar 2021.

Vancouver:

Zhang S. Transcriptional Regulation of CYP3A4 and CYP2D6 by Small Heterodimer Partner. [Internet] [Thesis]. University of Illinois – Chicago; 2016. [cited 2021 Mar 06]. 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

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