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You searched for subject:(p450). Showing records 1 – 30 of 520 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 January 22, 2020. 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. 22 Jan 2020.

Vancouver:

Rhieu S. Electrochemical, biochemical, structural studies of cytochrome P450 monooxygenases involved in metabolism of vitamin D. [Internet] [Doctoral dissertation]. Brown University; 2011. [cited 2020 Jan 22]. 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 January 22, 2020. 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. 22 Jan 2020.

Vancouver:

Porro CS. Quantum mechanical/molecular mechanics studies of Cytochrome P450BM3. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2020 Jan 22]. 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 Georgia

3. McPhail, Brooks Tia'. The ontogeny of cytochrome P450 (CYP450) activity, expression and volatile organic compound (VOC) metabolism in Sprague-Dawley (S-D) rats.

Degree: PhD, Toxicology, 2008, University of Georgia

 CYP450 levels are altered by development and minimum metabolism occurs in the young due to an under developed hepatic system. A minimum amount of data… (more)

Subjects/Keywords: Cytochrome P450 (CYP450)

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APA (6th Edition):

McPhail, B. T. (2008). The ontogeny of cytochrome P450 (CYP450) activity, expression and volatile organic compound (VOC) metabolism in Sprague-Dawley (S-D) rats. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/mcphail_brooks_t_200808_phd

Chicago Manual of Style (16th Edition):

McPhail, Brooks Tia'. “The ontogeny of cytochrome P450 (CYP450) activity, expression and volatile organic compound (VOC) metabolism in Sprague-Dawley (S-D) rats.” 2008. Doctoral Dissertation, University of Georgia. Accessed January 22, 2020. http://purl.galileo.usg.edu/uga_etd/mcphail_brooks_t_200808_phd.

MLA Handbook (7th Edition):

McPhail, Brooks Tia'. “The ontogeny of cytochrome P450 (CYP450) activity, expression and volatile organic compound (VOC) metabolism in Sprague-Dawley (S-D) rats.” 2008. Web. 22 Jan 2020.

Vancouver:

McPhail BT. The ontogeny of cytochrome P450 (CYP450) activity, expression and volatile organic compound (VOC) metabolism in Sprague-Dawley (S-D) rats. [Internet] [Doctoral dissertation]. University of Georgia; 2008. [cited 2020 Jan 22]. Available from: http://purl.galileo.usg.edu/uga_etd/mcphail_brooks_t_200808_phd.

Council of Science Editors:

McPhail BT. The ontogeny of cytochrome P450 (CYP450) activity, expression and volatile organic compound (VOC) metabolism in Sprague-Dawley (S-D) rats. [Doctoral Dissertation]. University of Georgia; 2008. Available from: http://purl.galileo.usg.edu/uga_etd/mcphail_brooks_t_200808_phd


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 January 22, 2020. http://hdl.handle.net/2142/95533.

MLA Handbook (7th Edition):

Gregory, Michael Carlton. “Understanding the mechanism of androgen biosynthesis.” 2016. Web. 22 Jan 2020.

Vancouver:

Gregory MC. Understanding the mechanism of androgen biosynthesis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2020 Jan 22]. 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 January 22, 2020. 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. 22 Jan 2020.

Vancouver:

Moore CD. Dehydrogenation of Raloxifene by Cytochrome P450 3A4. [Internet] [Doctoral dissertation]. University of Utah; 2010. [cited 2020 Jan 22]. 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


Université de Montréal

6. Huguet, Jade. Études métaboliques des isoenzymes du cytochrome P450 exprimées dans les ventricules de cœurs humains .

Degree: 2017, Université de Montréal

 Les isoenzymes du CYP450 sont grandement impliquées dans le métabolisme oxydatif des médicaments et des variations dans leur activité (interactions médicamenteuses, polymorphismes génétiques) peuvent occasionner… (more)

Subjects/Keywords: Cytochrome P450; Métabolisme; Metabolism

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APA (6th Edition):

Huguet, J. (2017). Études métaboliques des isoenzymes du cytochrome P450 exprimées dans les ventricules de cœurs humains . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/18593

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):

Huguet, Jade. “Études métaboliques des isoenzymes du cytochrome P450 exprimées dans les ventricules de cœurs humains .” 2017. Thesis, Université de Montréal. Accessed January 22, 2020. http://hdl.handle.net/1866/18593.

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

MLA Handbook (7th Edition):

Huguet, Jade. “Études métaboliques des isoenzymes du cytochrome P450 exprimées dans les ventricules de cœurs humains .” 2017. Web. 22 Jan 2020.

Vancouver:

Huguet J. Études métaboliques des isoenzymes du cytochrome P450 exprimées dans les ventricules de cœurs humains . [Internet] [Thesis]. Université de Montréal; 2017. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/1866/18593.

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

Council of Science Editors:

Huguet J. Études métaboliques des isoenzymes du cytochrome P450 exprimées dans les ventricules de cœurs humains . [Thesis]. Université de Montréal; 2017. Available from: http://hdl.handle.net/1866/18593

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

7. 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 January 22, 2020. 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. 22 Jan 2020.

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 2020 Jan 22]. 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 Illinois – Urbana-Champaign

8. Niu, Guodong. Toxicity of mycotoxins to insects and underlying molecular and biochemical mechanisms.

Degree: PhD, 0324, 2010, University of Illinois – Urbana-Champaign

 Mycotoxins are synthesized by fungi and released as secondary metabolites toxic to many animal species. The structurally diverse mycotoxins can be carcinogenic, mutagenic, teratogenic, estrogenic,… (more)

Subjects/Keywords: mycotoxin; cytochrome P450; toxicity; insect

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APA (6th Edition):

Niu, G. (2010). Toxicity of mycotoxins to insects and underlying molecular and biochemical mechanisms. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/17002

Chicago Manual of Style (16th Edition):

Niu, Guodong. “Toxicity of mycotoxins to insects and underlying molecular and biochemical mechanisms.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed January 22, 2020. http://hdl.handle.net/2142/17002.

MLA Handbook (7th Edition):

Niu, Guodong. “Toxicity of mycotoxins to insects and underlying molecular and biochemical mechanisms.” 2010. Web. 22 Jan 2020.

Vancouver:

Niu G. Toxicity of mycotoxins to insects and underlying molecular and biochemical mechanisms. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/2142/17002.

Council of Science Editors:

Niu G. Toxicity of mycotoxins to insects and underlying molecular and biochemical mechanisms. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/17002


University of Manchester

9. 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 January 22, 2020. 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. 22 Jan 2020.

Vancouver:

Matthews S. Characterisation and Engineering of Alkene Producing P450 Peroxygenases for Bioenergy Applications. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2020 Jan 22]. 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

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

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 January 22, 2020. 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. 22 Jan 2020.

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 2020 Jan 22]. 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 Adelaide

11. 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 January 22, 2020. 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. 22 Jan 2020.

Vancouver:

Lee JHZ. Harnessing P450 enzymes as biocatalysts for selective C-H bond hydroxylation. [Internet] [Thesis]. University of Adelaide; 2018. [cited 2020 Jan 22]. 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 Adelaide

12. Lau, Ian. Isolation of new P450s and the modification of existing P450s for biocatalysis.

Degree: 2017, University of Adelaide

 Cytochrome P450s are a family of heme-containing monooxygenases that are ubiquitous in nature. Many P450s from bacterial sources, such as from Frankia sp. EuI1c which… (more)

Subjects/Keywords: chemistry; cytochrome P450; biocatalysis

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APA (6th Edition):

Lau, I. (2017). Isolation of new P450s and the modification of existing P450s for biocatalysis. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/109793

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):

Lau, Ian. “Isolation of new P450s and the modification of existing P450s for biocatalysis.” 2017. Thesis, University of Adelaide. Accessed January 22, 2020. http://hdl.handle.net/2440/109793.

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

MLA Handbook (7th Edition):

Lau, Ian. “Isolation of new P450s and the modification of existing P450s for biocatalysis.” 2017. Web. 22 Jan 2020.

Vancouver:

Lau I. Isolation of new P450s and the modification of existing P450s for biocatalysis. [Internet] [Thesis]. University of Adelaide; 2017. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/2440/109793.

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

Council of Science Editors:

Lau I. Isolation of new P450s and the modification of existing P450s for biocatalysis. [Thesis]. University of Adelaide; 2017. Available from: http://hdl.handle.net/2440/109793

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


Cornell University

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

Degree: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/31140

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):

Bardowell, Sabrina. “The Role Of Vitamin E Hydroxylases In Vitamin E Metabolism And Status .” 2012. Thesis, Cornell University. Accessed January 22, 2020. http://hdl.handle.net/1813/31140.

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

MLA Handbook (7th Edition):

Bardowell, Sabrina. “The Role Of Vitamin E Hydroxylases In Vitamin E Metabolism And Status .” 2012. Web. 22 Jan 2020.

Vancouver:

Bardowell S. The Role Of Vitamin E Hydroxylases In Vitamin E Metabolism And Status . [Internet] [Thesis]. Cornell University; 2012. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/1813/31140.

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

Council of Science Editors:

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

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


University of Guelph

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

Degree: 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. (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9464

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):

Darch, Maryse. “Role of the Cytochrome P450 2A5 in Bilirubin Metabolism and Clearance in C57BL/6 Mice. ” 2016. Thesis, University of Guelph. Accessed January 22, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9464.

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

MLA Handbook (7th Edition):

Darch, Maryse. “Role of the Cytochrome P450 2A5 in Bilirubin Metabolism and Clearance in C57BL/6 Mice. ” 2016. Web. 22 Jan 2020.

Vancouver:

Darch M. Role of the Cytochrome P450 2A5 in Bilirubin Metabolism and Clearance in C57BL/6 Mice. [Internet] [Thesis]. University of Guelph; 2016. [cited 2020 Jan 22]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9464.

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

Council of Science Editors:

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

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


University of Texas – Austin

15. 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 January 22, 2020. http://hdl.handle.net/2152/46526.

MLA Handbook (7th Edition):

Sunnadeniya, Rasika Mayanthi. “Identification and functional analysis of betalain pathway genes.” 2014. Web. 22 Jan 2020.

Vancouver:

Sunnadeniya RM. Identification and functional analysis of betalain pathway genes. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Jan 22]. 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

16. 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 (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 January 22, 2020. 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. 22 Jan 2020.

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 2020 Jan 22]. 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

17. 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 (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 January 22, 2020. 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. 22 Jan 2020.

Vancouver:

Povsic M. Rational redesign of cytochrome P450 BM3 (CYP102A1) towards industrially relevant drug metabolites. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2020 Jan 22]. 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

18. 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: cytochrome P450; P450 BM3; drug metabolites; protein engineering; biotechnology

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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 January 22, 2020. 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. 22 Jan 2020.

Vancouver:

Povsic M. Rational redesign of cytochrome P450 BM3 (CYP102A1) towards industrially relevant drug metabolites. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2020 Jan 22]. 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

19. 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 January 22, 2020. 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. 22 Jan 2020.

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 2020 Jan 22]. 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


Texas A&M University

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

Degree: 2009, Texas A&M University

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

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

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APA (6th Edition):

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

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):

Gu, Xinsheng. “Regulation of cytochrome P450 3A4 gene expression through modulating pregnane X receptor transcriptional activity by NF-? aryl hydrocarbon receptor and xenobiotics.” 2009. Thesis, Texas A&M University. Accessed January 22, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-1630.

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

MLA Handbook (7th Edition):

Gu, Xinsheng. “Regulation of cytochrome P450 3A4 gene expression through modulating pregnane X receptor transcriptional activity by NF-? aryl hydrocarbon receptor and xenobiotics.” 2009. Web. 22 Jan 2020.

Vancouver:

Gu X. Regulation of cytochrome P450 3A4 gene expression through modulating pregnane X receptor transcriptional activity by NF-? aryl hydrocarbon receptor and xenobiotics. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1630.

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

Council of Science Editors:

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

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

21. 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 January 22, 2020. 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. 22 Jan 2020.

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 2020 Jan 22]. 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


University of Minnesota

22. Kramlinger, Valerie Marie. Characterization of b-nicotyrine-mediated inactivation of cytochrome P450 2A6.

Degree: PhD, Biochemistry, Molecular Bio, and Biophysics, 2013, University of Minnesota

 Nicotine, the primary addictive compound in cigarettes, is metabolized in humans by cytochrome P450 2A enzymes. The hepatic enzyme responsible for the metabolism of nicotine… (more)

Subjects/Keywords: Inactivation; Nicotine; Nicotyrine; P450 2A6; Smoking

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APA (6th Edition):

Kramlinger, V. M. (2013). Characterization of b-nicotyrine-mediated inactivation of cytochrome P450 2A6. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/163248

Chicago Manual of Style (16th Edition):

Kramlinger, Valerie Marie. “Characterization of b-nicotyrine-mediated inactivation of cytochrome P450 2A6.” 2013. Doctoral Dissertation, University of Minnesota. Accessed January 22, 2020. http://hdl.handle.net/11299/163248.

MLA Handbook (7th Edition):

Kramlinger, Valerie Marie. “Characterization of b-nicotyrine-mediated inactivation of cytochrome P450 2A6.” 2013. Web. 22 Jan 2020.

Vancouver:

Kramlinger VM. Characterization of b-nicotyrine-mediated inactivation of cytochrome P450 2A6. [Internet] [Doctoral dissertation]. University of Minnesota; 2013. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/11299/163248.

Council of Science Editors:

Kramlinger VM. Characterization of b-nicotyrine-mediated inactivation of cytochrome P450 2A6. [Doctoral Dissertation]. University of Minnesota; 2013. Available from: http://hdl.handle.net/11299/163248


University of Illinois – Urbana-Champaign

23. Lenov, Ivan Lenkov. Methodologies for the analysis of membrane systems using lipid nanodiscs.

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

 Membrane proteins are biologically significant targets of study due to their crucial roles in biochemical reactions, such as ion transport and cell signaling. Their study,… (more)

Subjects/Keywords: Nanodiscs; lipids; membrane; membrane protein; Cytochrome P450

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APA (6th Edition):

Lenov, I. L. (2016). Methodologies for the analysis of membrane systems using lipid nanodiscs. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/92994

Chicago Manual of Style (16th Edition):

Lenov, Ivan Lenkov. “Methodologies for the analysis of membrane systems using lipid nanodiscs.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed January 22, 2020. http://hdl.handle.net/2142/92994.

MLA Handbook (7th Edition):

Lenov, Ivan Lenkov. “Methodologies for the analysis of membrane systems using lipid nanodiscs.” 2016. Web. 22 Jan 2020.

Vancouver:

Lenov IL. Methodologies for the analysis of membrane systems using lipid nanodiscs. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/2142/92994.

Council of Science Editors:

Lenov IL. Methodologies for the analysis of membrane systems using lipid nanodiscs. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/92994


University of Illinois – Urbana-Champaign

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

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

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Frank, Daniel J. “Global deconvolution of heterotropic cooperativity in cytochrome P450 3A4.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed January 22, 2020. http://hdl.handle.net/2142/24520.

MLA Handbook (7th Edition):

Frank, Daniel J. “Global deconvolution of heterotropic cooperativity in cytochrome P450 3A4.” 2011. Web. 22 Jan 2020.

Vancouver:

Frank DJ. Global deconvolution of heterotropic cooperativity in cytochrome P450 3A4. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/2142/24520.

Council of Science Editors:

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


Ohio University

25. Withers, John C. CHARACTERIZATION OF TWO NOVEL CYTOCHROME P450S INVOLVED IN GRAVITROPISM IN ARABIDOPSIS THALIANA.

Degree: MS, Plant Biology (Arts and Sciences), 2007, Ohio University

 Understanding gene expression that occurs during gravitropism is important for studying the processes that link the perception of gravity to the growth response. The gravity… (more)

Subjects/Keywords: Plant gravitropism; Auxin; Flavonoids; Cytochrome P450

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APA (6th Edition):

Withers, J. C. (2007). CHARACTERIZATION OF TWO NOVEL CYTOCHROME P450S INVOLVED IN GRAVITROPISM IN ARABIDOPSIS THALIANA. (Masters Thesis). Ohio University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1187184960

Chicago Manual of Style (16th Edition):

Withers, John C. “CHARACTERIZATION OF TWO NOVEL CYTOCHROME P450S INVOLVED IN GRAVITROPISM IN ARABIDOPSIS THALIANA.” 2007. Masters Thesis, Ohio University. Accessed January 22, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1187184960.

MLA Handbook (7th Edition):

Withers, John C. “CHARACTERIZATION OF TWO NOVEL CYTOCHROME P450S INVOLVED IN GRAVITROPISM IN ARABIDOPSIS THALIANA.” 2007. Web. 22 Jan 2020.

Vancouver:

Withers JC. CHARACTERIZATION OF TWO NOVEL CYTOCHROME P450S INVOLVED IN GRAVITROPISM IN ARABIDOPSIS THALIANA. [Internet] [Masters thesis]. Ohio University; 2007. [cited 2020 Jan 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1187184960.

Council of Science Editors:

Withers JC. CHARACTERIZATION OF TWO NOVEL CYTOCHROME P450S INVOLVED IN GRAVITROPISM IN ARABIDOPSIS THALIANA. [Masters Thesis]. Ohio University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1187184960


Penn State University

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

Degree: PhD, Chemistry, 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. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/16041

Chicago Manual of Style (16th Edition):

Yosca, Timothy Howard. “Understanding C-H Bond Activation in Heme Proteins: The Importance of the Ferryl pKa.” 2012. Doctoral Dissertation, Penn State University. Accessed January 22, 2020. https://etda.libraries.psu.edu/catalog/16041.

MLA Handbook (7th Edition):

Yosca, Timothy Howard. “Understanding C-H Bond Activation in Heme Proteins: The Importance of the Ferryl pKa.” 2012. Web. 22 Jan 2020.

Vancouver:

Yosca TH. Understanding C-H Bond Activation in Heme Proteins: The Importance of the Ferryl pKa. [Internet] [Doctoral dissertation]. Penn State University; 2012. [cited 2020 Jan 22]. Available from: https://etda.libraries.psu.edu/catalog/16041.

Council of Science Editors:

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


University of Manchester

27. Elliott, Peter. Characterisation of the unique Campylobacter jejuni cytochrome P450, CYP172A1.

Degree: PhD, 2013, University of Manchester

 Campylobacter jejuni is a leading cause of food poisoning and according to the World Health Organisation accounts for majority of the 4.5 billion cases of… (more)

Subjects/Keywords: 616.9; Cytochrome P450; CYP172A1; Campylobacter jejuni; Capsule

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

APA (6th Edition):

Elliott, P. (2013). Characterisation of the unique Campylobacter jejuni cytochrome P450, CYP172A1. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-the-unique-campylobacter-jejuni-cytochrome-p450-cyp172a1(760b6cf4-f951-4642-9d99-b05b9a13ede2).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607029

Chicago Manual of Style (16th Edition):

Elliott, Peter. “Characterisation of the unique Campylobacter jejuni cytochrome P450, CYP172A1.” 2013. Doctoral Dissertation, University of Manchester. Accessed January 22, 2020. https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-the-unique-campylobacter-jejuni-cytochrome-p450-cyp172a1(760b6cf4-f951-4642-9d99-b05b9a13ede2).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607029.

MLA Handbook (7th Edition):

Elliott, Peter. “Characterisation of the unique Campylobacter jejuni cytochrome P450, CYP172A1.” 2013. Web. 22 Jan 2020.

Vancouver:

Elliott P. Characterisation of the unique Campylobacter jejuni cytochrome P450, CYP172A1. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2020 Jan 22]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-the-unique-campylobacter-jejuni-cytochrome-p450-cyp172a1(760b6cf4-f951-4642-9d99-b05b9a13ede2).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607029.

Council of Science Editors:

Elliott P. Characterisation of the unique Campylobacter jejuni cytochrome P450, CYP172A1. [Doctoral Dissertation]. University of Manchester; 2013. Available from: https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-the-unique-campylobacter-jejuni-cytochrome-p450-cyp172a1(760b6cf4-f951-4642-9d99-b05b9a13ede2).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607029


University of Manchester

28. 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 January 22, 2020. 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. 22 Jan 2020.

Vancouver:

Driscoll M. Investigating orphan cytochromes P450 from Mycobacterium tuberculosis : the search for potential drug targets. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2020 Jan 22]. 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


University of Manchester

29. Robinson, Jacob. Characterisation of novel cytochrome P450 fusion systems.

Degree: PhD, 2010, University of Manchester

 The biophysical and spectroscopic characterisation of two novel P450 fusion enzymes is reported. The first of these is CYP102A3, which is a fusion of P450(more)

Subjects/Keywords: 572.7; cytochrome P450; thiocarbamate; BM3; CYP102; CYP116

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

APA (6th Edition):

Robinson, J. (2010). Characterisation of novel cytochrome P450 fusion systems. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-novel-cytochrome-p450-fusion-systems(5b0847b2-8a5d-427d-9434-11a50f24311c).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.553252

Chicago Manual of Style (16th Edition):

Robinson, Jacob. “Characterisation of novel cytochrome P450 fusion systems.” 2010. Doctoral Dissertation, University of Manchester. Accessed January 22, 2020. https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-novel-cytochrome-p450-fusion-systems(5b0847b2-8a5d-427d-9434-11a50f24311c).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.553252.

MLA Handbook (7th Edition):

Robinson, Jacob. “Characterisation of novel cytochrome P450 fusion systems.” 2010. Web. 22 Jan 2020.

Vancouver:

Robinson J. Characterisation of novel cytochrome P450 fusion systems. [Internet] [Doctoral dissertation]. University of Manchester; 2010. [cited 2020 Jan 22]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-novel-cytochrome-p450-fusion-systems(5b0847b2-8a5d-427d-9434-11a50f24311c).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.553252.

Council of Science Editors:

Robinson J. Characterisation of novel cytochrome P450 fusion systems. [Doctoral Dissertation]. University of Manchester; 2010. Available from: https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-novel-cytochrome-p450-fusion-systems(5b0847b2-8a5d-427d-9434-11a50f24311c).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.553252


University of Saskatchewan

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

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 January 22, 2020. 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. 22 Jan 2020.

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 2020 Jan 22]. 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

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