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You searched for subject:(Enzyme inhibitors). Showing records 1 – 30 of 342 total matches.

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University of Alberta

1. Albohy, Amgad M R. Structure-based design of inhibitors for the human neuraminidase enzymes NEU2, NEU3, and NEU4.

Degree: PhD, Department of Chemistry, 2014, University of Alberta

 Sialidases (neuraminidases) are a group of enzymes responsible for the hydrolysis of sialic acid from glycoconjugates. In humans, there are four different isoenzymes that play… (more)

Subjects/Keywords: Human sialidases; Enzyme inhibitors; Neuraminidases

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APA (6th Edition):

Albohy, A. M. R. (2014). Structure-based design of inhibitors for the human neuraminidase enzymes NEU2, NEU3, and NEU4. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/5d86p310z

Chicago Manual of Style (16th Edition):

Albohy, Amgad M R. “Structure-based design of inhibitors for the human neuraminidase enzymes NEU2, NEU3, and NEU4.” 2014. Doctoral Dissertation, University of Alberta. Accessed April 19, 2021. https://era.library.ualberta.ca/files/5d86p310z.

MLA Handbook (7th Edition):

Albohy, Amgad M R. “Structure-based design of inhibitors for the human neuraminidase enzymes NEU2, NEU3, and NEU4.” 2014. Web. 19 Apr 2021.

Vancouver:

Albohy AMR. Structure-based design of inhibitors for the human neuraminidase enzymes NEU2, NEU3, and NEU4. [Internet] [Doctoral dissertation]. University of Alberta; 2014. [cited 2021 Apr 19]. Available from: https://era.library.ualberta.ca/files/5d86p310z.

Council of Science Editors:

Albohy AMR. Structure-based design of inhibitors for the human neuraminidase enzymes NEU2, NEU3, and NEU4. [Doctoral Dissertation]. University of Alberta; 2014. Available from: https://era.library.ualberta.ca/files/5d86p310z


University of Texas Southwestern Medical Center

2. Holohan, Brody Christopher. Identifying, Characterizing and Inhibiting the Telomerase Regulatory Network.

Degree: 2015, University of Texas Southwestern Medical Center

 Telomeres, which are structures that cap the ends of linear chromosomes are maintained by telomerase, a reverse transcriptase. Telomere length limits the self-renewal capacity for… (more)

Subjects/Keywords: Enzyme Inhibitors; Neoplasms; Phosphorylcholine; Telomerase

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APA (6th Edition):

Holohan, B. C. (2015). Identifying, Characterizing and Inhibiting the Telomerase Regulatory Network. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5288

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):

Holohan, Brody Christopher. “Identifying, Characterizing and Inhibiting the Telomerase Regulatory Network.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed April 19, 2021. http://hdl.handle.net/2152.5/5288.

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

MLA Handbook (7th Edition):

Holohan, Brody Christopher. “Identifying, Characterizing and Inhibiting the Telomerase Regulatory Network.” 2015. Web. 19 Apr 2021.

Vancouver:

Holohan BC. Identifying, Characterizing and Inhibiting the Telomerase Regulatory Network. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/2152.5/5288.

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

Council of Science Editors:

Holohan BC. Identifying, Characterizing and Inhibiting the Telomerase Regulatory Network. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/5288

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


Massey University

3. Barzak, Fareeda Maged Yahya Mohammad. Biophysical and biochemical characterisation of DNA-based inhibitors of the cytosine-mutating APOBEC3 enzymes.

Degree: PhD, Biochemistry, 2020, Massey University

 With the rise of antiviral and anticancer drug resistance, a new approach must be taken to overcome this burden. The APOBEC3 (A3) family of cytosine… (more)

Subjects/Keywords: Enzymes; Enzyme inhibitors; Cancer; Treatment

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APA (6th Edition):

Barzak, F. M. Y. M. (2020). Biophysical and biochemical characterisation of DNA-based inhibitors of the cytosine-mutating APOBEC3 enzymes. (Doctoral Dissertation). Massey University. Retrieved from http://hdl.handle.net/10179/16128

Chicago Manual of Style (16th Edition):

Barzak, Fareeda Maged Yahya Mohammad. “Biophysical and biochemical characterisation of DNA-based inhibitors of the cytosine-mutating APOBEC3 enzymes.” 2020. Doctoral Dissertation, Massey University. Accessed April 19, 2021. http://hdl.handle.net/10179/16128.

MLA Handbook (7th Edition):

Barzak, Fareeda Maged Yahya Mohammad. “Biophysical and biochemical characterisation of DNA-based inhibitors of the cytosine-mutating APOBEC3 enzymes.” 2020. Web. 19 Apr 2021.

Vancouver:

Barzak FMYM. Biophysical and biochemical characterisation of DNA-based inhibitors of the cytosine-mutating APOBEC3 enzymes. [Internet] [Doctoral dissertation]. Massey University; 2020. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/10179/16128.

Council of Science Editors:

Barzak FMYM. Biophysical and biochemical characterisation of DNA-based inhibitors of the cytosine-mutating APOBEC3 enzymes. [Doctoral Dissertation]. Massey University; 2020. Available from: http://hdl.handle.net/10179/16128


Oregon State University

4. Wu, Paiyen. Effects of various protease inhibitors on protein degradation of cultured myotubes.

Degree: MS, Animal Science, 1996, Oregon State University

Subjects/Keywords: Proteolytic enzyme inhibitors

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APA (6th Edition):

Wu, P. (1996). Effects of various protease inhibitors on protein degradation of cultured myotubes. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/34999

Chicago Manual of Style (16th Edition):

Wu, Paiyen. “Effects of various protease inhibitors on protein degradation of cultured myotubes.” 1996. Masters Thesis, Oregon State University. Accessed April 19, 2021. http://hdl.handle.net/1957/34999.

MLA Handbook (7th Edition):

Wu, Paiyen. “Effects of various protease inhibitors on protein degradation of cultured myotubes.” 1996. Web. 19 Apr 2021.

Vancouver:

Wu P. Effects of various protease inhibitors on protein degradation of cultured myotubes. [Internet] [Masters thesis]. Oregon State University; 1996. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/1957/34999.

Council of Science Editors:

Wu P. Effects of various protease inhibitors on protein degradation of cultured myotubes. [Masters Thesis]. Oregon State University; 1996. Available from: http://hdl.handle.net/1957/34999


Rhodes University

5. Manyeruke, Meloddy Hlatini. Application of Baylis-Hillman methodology in the synthesis of HIV-1 enzyme inhibitors.

Degree: MS, Faculty of Science, Chemistry, 2015, Rhodes University

 The application of Baylis-Hillman methodology has afforded access to a range of β-hydroxypropionate ester-AZT conjugates as potential dual-action HIV-1 IN/RT inhibitors. Two families comprising a… (more)

Subjects/Keywords: HIV infections; Enzyme inhibitors; AZT (Drug); Bioconjugates

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APA (6th Edition):

Manyeruke, M. H. (2015). Application of Baylis-Hillman methodology in the synthesis of HIV-1 enzyme inhibitors. (Masters Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1017920

Chicago Manual of Style (16th Edition):

Manyeruke, Meloddy Hlatini. “Application of Baylis-Hillman methodology in the synthesis of HIV-1 enzyme inhibitors.” 2015. Masters Thesis, Rhodes University. Accessed April 19, 2021. http://hdl.handle.net/10962/d1017920.

MLA Handbook (7th Edition):

Manyeruke, Meloddy Hlatini. “Application of Baylis-Hillman methodology in the synthesis of HIV-1 enzyme inhibitors.” 2015. Web. 19 Apr 2021.

Vancouver:

Manyeruke MH. Application of Baylis-Hillman methodology in the synthesis of HIV-1 enzyme inhibitors. [Internet] [Masters thesis]. Rhodes University; 2015. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/10962/d1017920.

Council of Science Editors:

Manyeruke MH. Application of Baylis-Hillman methodology in the synthesis of HIV-1 enzyme inhibitors. [Masters Thesis]. Rhodes University; 2015. Available from: http://hdl.handle.net/10962/d1017920


Rhodes University

6. Sekgota, Khethobole Cassius. Design, development and evaluation of novel lead compounds as HIV-1 enzyme inhibitors.

Degree: MS, Faculty of Science, Chemistry, 2015, Rhodes University

 This project has been concerned with the application of the Baylis-Hillman methodology to the synthesis of medicinally important diketo acid analogues (cinnamate ester-AZT conjugates and… (more)

Subjects/Keywords: Enzyme inhibitors; Viruses  – Reproduction; HIV (Viruses)

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APA (6th Edition):

Sekgota, K. C. (2015). Design, development and evaluation of novel lead compounds as HIV-1 enzyme inhibitors. (Masters Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1017926

Chicago Manual of Style (16th Edition):

Sekgota, Khethobole Cassius. “Design, development and evaluation of novel lead compounds as HIV-1 enzyme inhibitors.” 2015. Masters Thesis, Rhodes University. Accessed April 19, 2021. http://hdl.handle.net/10962/d1017926.

MLA Handbook (7th Edition):

Sekgota, Khethobole Cassius. “Design, development and evaluation of novel lead compounds as HIV-1 enzyme inhibitors.” 2015. Web. 19 Apr 2021.

Vancouver:

Sekgota KC. Design, development and evaluation of novel lead compounds as HIV-1 enzyme inhibitors. [Internet] [Masters thesis]. Rhodes University; 2015. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/10962/d1017926.

Council of Science Editors:

Sekgota KC. Design, development and evaluation of novel lead compounds as HIV-1 enzyme inhibitors. [Masters Thesis]. Rhodes University; 2015. Available from: http://hdl.handle.net/10962/d1017926

7. Badmus, Abimbola Adesile. The allelopathic potential of Arctotis Arctotoides (L.f.) O. Hoffm on some vegetables.

Degree: PhD, Botany, 2012, University of Fort Hare

 Laboratory and greenhouse experiments were conducted to evaluate the allelopathic effects of the extracts and residue Arctotis arctotoides (L.f.) O. Hoffm on selected vegetable crops.… (more)

Subjects/Keywords: Allelopathy; Allelopathic agents; Vegetables – Microbiology; Enzyme inhibitors

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APA (6th Edition):

Badmus, A. A. (2012). The allelopathic potential of Arctotis Arctotoides (L.f.) O. Hoffm on some vegetables. (Doctoral Dissertation). University of Fort Hare. Retrieved from http://hdl.handle.net/10353/454

Chicago Manual of Style (16th Edition):

Badmus, Abimbola Adesile. “The allelopathic potential of Arctotis Arctotoides (L.f.) O. Hoffm on some vegetables.” 2012. Doctoral Dissertation, University of Fort Hare. Accessed April 19, 2021. http://hdl.handle.net/10353/454.

MLA Handbook (7th Edition):

Badmus, Abimbola Adesile. “The allelopathic potential of Arctotis Arctotoides (L.f.) O. Hoffm on some vegetables.” 2012. Web. 19 Apr 2021.

Vancouver:

Badmus AA. The allelopathic potential of Arctotis Arctotoides (L.f.) O. Hoffm on some vegetables. [Internet] [Doctoral dissertation]. University of Fort Hare; 2012. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/10353/454.

Council of Science Editors:

Badmus AA. The allelopathic potential of Arctotis Arctotoides (L.f.) O. Hoffm on some vegetables. [Doctoral Dissertation]. University of Fort Hare; 2012. Available from: http://hdl.handle.net/10353/454


Oregon State University

8. Hong, Dong-Hyun. Endocrine control of proteolysis in cultured muscle cells.

Degree: PhD, Animal Science, 1993, Oregon State University

Subjects/Keywords: Proteolytic enzyme inhibitors

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APA (6th Edition):

Hong, D. (1993). Endocrine control of proteolysis in cultured muscle cells. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/35450

Chicago Manual of Style (16th Edition):

Hong, Dong-Hyun. “Endocrine control of proteolysis in cultured muscle cells.” 1993. Doctoral Dissertation, Oregon State University. Accessed April 19, 2021. http://hdl.handle.net/1957/35450.

MLA Handbook (7th Edition):

Hong, Dong-Hyun. “Endocrine control of proteolysis in cultured muscle cells.” 1993. Web. 19 Apr 2021.

Vancouver:

Hong D. Endocrine control of proteolysis in cultured muscle cells. [Internet] [Doctoral dissertation]. Oregon State University; 1993. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/1957/35450.

Council of Science Editors:

Hong D. Endocrine control of proteolysis in cultured muscle cells. [Doctoral Dissertation]. Oregon State University; 1993. Available from: http://hdl.handle.net/1957/35450


Columbia University

9. Viswanathan, Vasanthi. Cellular features predicting susceptibility to ferroptosis: insights from cancer cell-line profiling.

Degree: 2015, Columbia University

 Ferroptosis is a novel non-apoptotic, oxidative form of regulated cell death that can be triggered by diverse small-molecule ferroptosis inducers (FINs) and genetic perturbations. Current… (more)

Subjects/Keywords: Cancer; Enzyme inhibitors; Cell death; Cytology

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APA (6th Edition):

Viswanathan, V. (2015). Cellular features predicting susceptibility to ferroptosis: insights from cancer cell-line profiling. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8H9940V

Chicago Manual of Style (16th Edition):

Viswanathan, Vasanthi. “Cellular features predicting susceptibility to ferroptosis: insights from cancer cell-line profiling.” 2015. Doctoral Dissertation, Columbia University. Accessed April 19, 2021. https://doi.org/10.7916/D8H9940V.

MLA Handbook (7th Edition):

Viswanathan, Vasanthi. “Cellular features predicting susceptibility to ferroptosis: insights from cancer cell-line profiling.” 2015. Web. 19 Apr 2021.

Vancouver:

Viswanathan V. Cellular features predicting susceptibility to ferroptosis: insights from cancer cell-line profiling. [Internet] [Doctoral dissertation]. Columbia University; 2015. [cited 2021 Apr 19]. Available from: https://doi.org/10.7916/D8H9940V.

Council of Science Editors:

Viswanathan V. Cellular features predicting susceptibility to ferroptosis: insights from cancer cell-line profiling. [Doctoral Dissertation]. Columbia University; 2015. Available from: https://doi.org/10.7916/D8H9940V


University of Bath

10. Sage, Matthew Arthur. Synthesis of peptide mimetics.

Degree: PhD, 1995, University of Bath

Subjects/Keywords: 572; Enzyme inhibitors

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APA (6th Edition):

Sage, M. A. (1995). Synthesis of peptide mimetics. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/synthesis-of-peptide-mimetics(20829dc8-1b3b-4051-adf1-2bdff6917625).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.261380

Chicago Manual of Style (16th Edition):

Sage, Matthew Arthur. “Synthesis of peptide mimetics.” 1995. Doctoral Dissertation, University of Bath. Accessed April 19, 2021. https://researchportal.bath.ac.uk/en/studentthesis/synthesis-of-peptide-mimetics(20829dc8-1b3b-4051-adf1-2bdff6917625).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.261380.

MLA Handbook (7th Edition):

Sage, Matthew Arthur. “Synthesis of peptide mimetics.” 1995. Web. 19 Apr 2021.

Vancouver:

Sage MA. Synthesis of peptide mimetics. [Internet] [Doctoral dissertation]. University of Bath; 1995. [cited 2021 Apr 19]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/synthesis-of-peptide-mimetics(20829dc8-1b3b-4051-adf1-2bdff6917625).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.261380.

Council of Science Editors:

Sage MA. Synthesis of peptide mimetics. [Doctoral Dissertation]. University of Bath; 1995. Available from: https://researchportal.bath.ac.uk/en/studentthesis/synthesis-of-peptide-mimetics(20829dc8-1b3b-4051-adf1-2bdff6917625).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.261380


University of Manchester

11. Obi, Juliana. Synthesis of analogues of dicoumarol and their measurement as inhibitors of NQO1.

Degree: PhD, 2016, University of Manchester

 A variety of novel and effective inhibitors of NQO1 was synthesized. The inhibitors were classified as 'asymmetrical' and 'halfway stage' analogues of dicoumarol. The synthesis… (more)

Subjects/Keywords: 572; Synthesis; Inhibitors; Enzyme and MTT assays

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APA (6th Edition):

Obi, J. (2016). Synthesis of analogues of dicoumarol and their measurement as inhibitors of NQO1. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/synthesis-of-analogues-of-dicoumaroland-their-measurementas-inhibitors-of-nqo1(985aa4d2-437d-46ff-aadd-8f72ab9887c9).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727885

Chicago Manual of Style (16th Edition):

Obi, Juliana. “Synthesis of analogues of dicoumarol and their measurement as inhibitors of NQO1.” 2016. Doctoral Dissertation, University of Manchester. Accessed April 19, 2021. https://www.research.manchester.ac.uk/portal/en/theses/synthesis-of-analogues-of-dicoumaroland-their-measurementas-inhibitors-of-nqo1(985aa4d2-437d-46ff-aadd-8f72ab9887c9).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727885.

MLA Handbook (7th Edition):

Obi, Juliana. “Synthesis of analogues of dicoumarol and their measurement as inhibitors of NQO1.” 2016. Web. 19 Apr 2021.

Vancouver:

Obi J. Synthesis of analogues of dicoumarol and their measurement as inhibitors of NQO1. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2021 Apr 19]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/synthesis-of-analogues-of-dicoumaroland-their-measurementas-inhibitors-of-nqo1(985aa4d2-437d-46ff-aadd-8f72ab9887c9).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727885.

Council of Science Editors:

Obi J. Synthesis of analogues of dicoumarol and their measurement as inhibitors of NQO1. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/synthesis-of-analogues-of-dicoumaroland-their-measurementas-inhibitors-of-nqo1(985aa4d2-437d-46ff-aadd-8f72ab9887c9).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727885

12. McCarthy, Sean Joseph. Strained amides as potential antibacterials.

Degree: PhD, 1996, University of Sussex

Subjects/Keywords: 660; Enzyme inhibitors

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APA (6th Edition):

McCarthy, S. J. (1996). Strained amides as potential antibacterials. (Doctoral Dissertation). University of Sussex. Retrieved from https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296003

Chicago Manual of Style (16th Edition):

McCarthy, Sean Joseph. “Strained amides as potential antibacterials.” 1996. Doctoral Dissertation, University of Sussex. Accessed April 19, 2021. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296003.

MLA Handbook (7th Edition):

McCarthy, Sean Joseph. “Strained amides as potential antibacterials.” 1996. Web. 19 Apr 2021.

Vancouver:

McCarthy SJ. Strained amides as potential antibacterials. [Internet] [Doctoral dissertation]. University of Sussex; 1996. [cited 2021 Apr 19]. Available from: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296003.

Council of Science Editors:

McCarthy SJ. Strained amides as potential antibacterials. [Doctoral Dissertation]. University of Sussex; 1996. Available from: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296003


University of Arizona

13. Schuster, Sheldon Mark, 1947-. THE REGULATION OF THE PYRUVATE DEHYDROGENASE MULTIENZYME COMPLEX BY CALCIUM AND MAGNESIUM IN HEART MITOCHONDRIAL SYSTEMS .

Degree: 1974, University of Arizona

Subjects/Keywords: Enzyme inhibitors.; Dehydrogenases.

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APA (6th Edition):

Schuster, Sheldon Mark, 1. (1974). THE REGULATION OF THE PYRUVATE DEHYDROGENASE MULTIENZYME COMPLEX BY CALCIUM AND MAGNESIUM IN HEART MITOCHONDRIAL SYSTEMS . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/288235

Chicago Manual of Style (16th Edition):

Schuster, Sheldon Mark, 1947-. “THE REGULATION OF THE PYRUVATE DEHYDROGENASE MULTIENZYME COMPLEX BY CALCIUM AND MAGNESIUM IN HEART MITOCHONDRIAL SYSTEMS .” 1974. Doctoral Dissertation, University of Arizona. Accessed April 19, 2021. http://hdl.handle.net/10150/288235.

MLA Handbook (7th Edition):

Schuster, Sheldon Mark, 1947-. “THE REGULATION OF THE PYRUVATE DEHYDROGENASE MULTIENZYME COMPLEX BY CALCIUM AND MAGNESIUM IN HEART MITOCHONDRIAL SYSTEMS .” 1974. Web. 19 Apr 2021.

Vancouver:

Schuster, Sheldon Mark 1. THE REGULATION OF THE PYRUVATE DEHYDROGENASE MULTIENZYME COMPLEX BY CALCIUM AND MAGNESIUM IN HEART MITOCHONDRIAL SYSTEMS . [Internet] [Doctoral dissertation]. University of Arizona; 1974. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/10150/288235.

Council of Science Editors:

Schuster, Sheldon Mark 1. THE REGULATION OF THE PYRUVATE DEHYDROGENASE MULTIENZYME COMPLEX BY CALCIUM AND MAGNESIUM IN HEART MITOCHONDRIAL SYSTEMS . [Doctoral Dissertation]. University of Arizona; 1974. Available from: http://hdl.handle.net/10150/288235


Georgia Tech

14. Whitley, Ronald Jay. An investigation of chymotrypsin A[gamma]inhibition with peptide aldehydes and related analogs ; II Inhibition of elastase by tetrapeptide chloromethyl ketones.

Degree: PhD, Chemistry, 1975, Georgia Tech

Subjects/Keywords: Enzyme inhibitors; Chymotrypsin

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APA (6th Edition):

Whitley, R. J. (1975). An investigation of chymotrypsin A[gamma]inhibition with peptide aldehydes and related analogs ; II Inhibition of elastase by tetrapeptide chloromethyl ketones. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/25989

Chicago Manual of Style (16th Edition):

Whitley, Ronald Jay. “An investigation of chymotrypsin A[gamma]inhibition with peptide aldehydes and related analogs ; II Inhibition of elastase by tetrapeptide chloromethyl ketones.” 1975. Doctoral Dissertation, Georgia Tech. Accessed April 19, 2021. http://hdl.handle.net/1853/25989.

MLA Handbook (7th Edition):

Whitley, Ronald Jay. “An investigation of chymotrypsin A[gamma]inhibition with peptide aldehydes and related analogs ; II Inhibition of elastase by tetrapeptide chloromethyl ketones.” 1975. Web. 19 Apr 2021.

Vancouver:

Whitley RJ. An investigation of chymotrypsin A[gamma]inhibition with peptide aldehydes and related analogs ; II Inhibition of elastase by tetrapeptide chloromethyl ketones. [Internet] [Doctoral dissertation]. Georgia Tech; 1975. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/1853/25989.

Council of Science Editors:

Whitley RJ. An investigation of chymotrypsin A[gamma]inhibition with peptide aldehydes and related analogs ; II Inhibition of elastase by tetrapeptide chloromethyl ketones. [Doctoral Dissertation]. Georgia Tech; 1975. Available from: http://hdl.handle.net/1853/25989


University of Manchester

15. Obi, Juliana. Synthesis of Analogues of Dicoumaroland their Measurementas Inhibitors of NQO1.

Degree: 2016, University of Manchester

 A variety of novel and effective inhibitors of NQO1 was synthesized. The inhibitors were classified as ‘asymmetrical’ and ‘halfway stage’ analogues of dicoumarol. The synthesis… (more)

Subjects/Keywords: Synthesis; Inhibitors; Enzyme and MTT assays

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APA (6th Edition):

Obi, J. (2016). Synthesis of Analogues of Dicoumaroland their Measurementas Inhibitors of NQO1. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301484

Chicago Manual of Style (16th Edition):

Obi, Juliana. “Synthesis of Analogues of Dicoumaroland their Measurementas Inhibitors of NQO1.” 2016. Doctoral Dissertation, University of Manchester. Accessed April 19, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301484.

MLA Handbook (7th Edition):

Obi, Juliana. “Synthesis of Analogues of Dicoumaroland their Measurementas Inhibitors of NQO1.” 2016. Web. 19 Apr 2021.

Vancouver:

Obi J. Synthesis of Analogues of Dicoumaroland their Measurementas Inhibitors of NQO1. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2021 Apr 19]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301484.

Council of Science Editors:

Obi J. Synthesis of Analogues of Dicoumaroland their Measurementas Inhibitors of NQO1. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301484


Cornell University

16. Mossino, Louna Marine. Fluorogenic Assay: High-Throughput Screening of Sirtuins' Activity and Inhibitors as Potential Therapeutic Agents.

Degree: M.S., Chemistry and Chemical Biology, Chemistry and Chemical Biology, 2020, Cornell University

 This thesis focuses on studying the effects of sirtuins, i.e. enzymes with important functions in the regulation of gene expression, especially because of their deacetylation… (more)

Subjects/Keywords: Cancer; Enzyme; Epigenetics; Fluorescence; Inhibitors; Sirtuin

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APA (6th Edition):

Mossino, L. M. (2020). Fluorogenic Assay: High-Throughput Screening of Sirtuins' Activity and Inhibitors as Potential Therapeutic Agents. (Masters Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/103136

Chicago Manual of Style (16th Edition):

Mossino, Louna Marine. “Fluorogenic Assay: High-Throughput Screening of Sirtuins' Activity and Inhibitors as Potential Therapeutic Agents.” 2020. Masters Thesis, Cornell University. Accessed April 19, 2021. http://hdl.handle.net/1813/103136.

MLA Handbook (7th Edition):

Mossino, Louna Marine. “Fluorogenic Assay: High-Throughput Screening of Sirtuins' Activity and Inhibitors as Potential Therapeutic Agents.” 2020. Web. 19 Apr 2021.

Vancouver:

Mossino LM. Fluorogenic Assay: High-Throughput Screening of Sirtuins' Activity and Inhibitors as Potential Therapeutic Agents. [Internet] [Masters thesis]. Cornell University; 2020. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/1813/103136.

Council of Science Editors:

Mossino LM. Fluorogenic Assay: High-Throughput Screening of Sirtuins' Activity and Inhibitors as Potential Therapeutic Agents. [Masters Thesis]. Cornell University; 2020. Available from: http://hdl.handle.net/1813/103136


Universidade Estadual de Campinas

17. Barbosa, Ademar Mesquita, 1973-. Utilização de inibidores enzimáticos em Leishmania amazonensis.

Degree: Instituto de Biologia; Programa de Pós-Graduação em Parasitologia, 2013, Universidade Estadual de Campinas

Orientador: Selma Giorgio

Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Biologia

Made available in DSpace on 2018-08-23T15:16:57Z (GMT). No. of bitstreams: 1 Barbosa_AdemarMesquita_M.pdf:… (more)

Subjects/Keywords: Inibidores enzimaticos; Leishmania; Enzyme inhibitors; Leishmania

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APA (6th Edition):

Barbosa, Ademar Mesquita, 1. (2013). Utilização de inibidores enzimáticos em Leishmania amazonensis. (Masters Thesis). Universidade Estadual de Campinas. Retrieved from BARBOSA, Ademar Mesquita. Utilização de inibidores enzimáticos em Leishmania amazonensis. 2013. 69 f. Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Biologia, Campinas, SP. Disponível em: <http://www.repositorio.unicamp.br/handle/REPOSIP/317485>. Acesso em: 23 ago. 2018. ; http://repositorio.unicamp.br/jspui/handle/REPOSIP/317485

Chicago Manual of Style (16th Edition):

Barbosa, Ademar Mesquita, 1973-. “Utilização de inibidores enzimáticos em Leishmania amazonensis.” 2013. Masters Thesis, Universidade Estadual de Campinas. Accessed April 19, 2021. BARBOSA, Ademar Mesquita. Utilização de inibidores enzimáticos em Leishmania amazonensis. 2013. 69 f. Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Biologia, Campinas, SP. Disponível em: <http://www.repositorio.unicamp.br/handle/REPOSIP/317485>. Acesso em: 23 ago. 2018. ; http://repositorio.unicamp.br/jspui/handle/REPOSIP/317485.

MLA Handbook (7th Edition):

Barbosa, Ademar Mesquita, 1973-. “Utilização de inibidores enzimáticos em Leishmania amazonensis.” 2013. Web. 19 Apr 2021.

Vancouver:

Barbosa, Ademar Mesquita 1. Utilização de inibidores enzimáticos em Leishmania amazonensis. [Internet] [Masters thesis]. Universidade Estadual de Campinas; 2013. [cited 2021 Apr 19]. Available from: BARBOSA, Ademar Mesquita. Utilização de inibidores enzimáticos em Leishmania amazonensis. 2013. 69 f. Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Biologia, Campinas, SP. Disponível em: <http://www.repositorio.unicamp.br/handle/REPOSIP/317485>. Acesso em: 23 ago. 2018. ; http://repositorio.unicamp.br/jspui/handle/REPOSIP/317485.

Council of Science Editors:

Barbosa, Ademar Mesquita 1. Utilização de inibidores enzimáticos em Leishmania amazonensis. [Masters Thesis]. Universidade Estadual de Campinas; 2013. Available from: BARBOSA, Ademar Mesquita. Utilização de inibidores enzimáticos em Leishmania amazonensis. 2013. 69 f. Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Biologia, Campinas, SP. Disponível em: <http://www.repositorio.unicamp.br/handle/REPOSIP/317485>. Acesso em: 23 ago. 2018. ; http://repositorio.unicamp.br/jspui/handle/REPOSIP/317485


Latrobe University

18. Brand, Ingo Lothar. Characterisation and identification of novel caspase inhibitors.

Degree: PhD, 2011, Latrobe University

Thesis (Ph.D.) - La Trobe University, 2011

Submission note: "A thesis submitted in total fulfilment of the requirements for the degree of Doctor of Philosophy… (more)

Subjects/Keywords: Protease inhibitors.; Apoptosis.; Virus-induced enzymes.; Viruses.; Enzyme inhibitors.

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APA (6th Edition):

Brand, I. L. (2011). Characterisation and identification of novel caspase inhibitors. (Doctoral Dissertation). Latrobe University. Retrieved from http://hdl.handle.net/1959.9/495861

Chicago Manual of Style (16th Edition):

Brand, Ingo Lothar. “Characterisation and identification of novel caspase inhibitors.” 2011. Doctoral Dissertation, Latrobe University. Accessed April 19, 2021. http://hdl.handle.net/1959.9/495861.

MLA Handbook (7th Edition):

Brand, Ingo Lothar. “Characterisation and identification of novel caspase inhibitors.” 2011. Web. 19 Apr 2021.

Vancouver:

Brand IL. Characterisation and identification of novel caspase inhibitors. [Internet] [Doctoral dissertation]. Latrobe University; 2011. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/1959.9/495861.

Council of Science Editors:

Brand IL. Characterisation and identification of novel caspase inhibitors. [Doctoral Dissertation]. Latrobe University; 2011. Available from: http://hdl.handle.net/1959.9/495861

19. Collins, Davis Earl. Investigating the inhibition of cytochrome P450 isoform 1A1 by açai berry (Euterpe oleracea) extracts using a bioassay guided fractionation approach.

Degree: 2016, NC Docks

 Xenobiotic metabolism is an important process within the human body, as it alters large, foreign, hydrophobic molecules and prepares them for excretion. This process is… (more)

Subjects/Keywords: Cytochrome P-450 $x Inhibitors; Enzyme inhibitors; Acai palm

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APA (6th Edition):

Collins, D. E. (2016). Investigating the inhibition of cytochrome P450 isoform 1A1 by açai berry (Euterpe oleracea) extracts using a bioassay guided fractionation approach. (Thesis). NC Docks. Retrieved from http://libres.uncg.edu/ir/uncg/f/Collins_uncg_0154M_12019.pdf

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):

Collins, Davis Earl. “Investigating the inhibition of cytochrome P450 isoform 1A1 by açai berry (Euterpe oleracea) extracts using a bioassay guided fractionation approach.” 2016. Thesis, NC Docks. Accessed April 19, 2021. http://libres.uncg.edu/ir/uncg/f/Collins_uncg_0154M_12019.pdf.

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

MLA Handbook (7th Edition):

Collins, Davis Earl. “Investigating the inhibition of cytochrome P450 isoform 1A1 by açai berry (Euterpe oleracea) extracts using a bioassay guided fractionation approach.” 2016. Web. 19 Apr 2021.

Vancouver:

Collins DE. Investigating the inhibition of cytochrome P450 isoform 1A1 by açai berry (Euterpe oleracea) extracts using a bioassay guided fractionation approach. [Internet] [Thesis]. NC Docks; 2016. [cited 2021 Apr 19]. Available from: http://libres.uncg.edu/ir/uncg/f/Collins_uncg_0154M_12019.pdf.

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

Council of Science Editors:

Collins DE. Investigating the inhibition of cytochrome P450 isoform 1A1 by açai berry (Euterpe oleracea) extracts using a bioassay guided fractionation approach. [Thesis]. NC Docks; 2016. Available from: http://libres.uncg.edu/ir/uncg/f/Collins_uncg_0154M_12019.pdf

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


Northeastern University

20. Tanner, Angela L. Exploration of structure-activity relationships of a kinase-targeting chemotype that suppresses Trypanosoma brucei.

Degree: MS, Department of Chemistry and Chemical Biology, 2015, Northeastern University

 Human African trypanosomiasis is a lethal neglected tropical disease in need of more effective and efficient treatment. In an effort to develop inhibitors of the… (more)

Subjects/Keywords: Trypanosoma brucei; tropical disease; kinase inhibitor; Enzyme inhibitors; Structure; Enzyme inhibitors; Synthesis; Protein kinases; Inhibitors; Structure; Protein kinases; Inhibitors; Synthesis; Chemical structure; Analysis; African trypanosomiasis; Prevention; Tropical medicine

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APA (6th Edition):

Tanner, A. L. (2015). Exploration of structure-activity relationships of a kinase-targeting chemotype that suppresses Trypanosoma brucei. (Masters Thesis). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20194223

Chicago Manual of Style (16th Edition):

Tanner, Angela L. “Exploration of structure-activity relationships of a kinase-targeting chemotype that suppresses Trypanosoma brucei.” 2015. Masters Thesis, Northeastern University. Accessed April 19, 2021. http://hdl.handle.net/2047/D20194223.

MLA Handbook (7th Edition):

Tanner, Angela L. “Exploration of structure-activity relationships of a kinase-targeting chemotype that suppresses Trypanosoma brucei.” 2015. Web. 19 Apr 2021.

Vancouver:

Tanner AL. Exploration of structure-activity relationships of a kinase-targeting chemotype that suppresses Trypanosoma brucei. [Internet] [Masters thesis]. Northeastern University; 2015. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/2047/D20194223.

Council of Science Editors:

Tanner AL. Exploration of structure-activity relationships of a kinase-targeting chemotype that suppresses Trypanosoma brucei. [Masters Thesis]. Northeastern University; 2015. Available from: http://hdl.handle.net/2047/D20194223


University of New South Wales

21. Sundaraneedi, Madhu Kiran. Targeting enzymes with oligonuclear ruthenium(II) complexes.

Degree: Physical, Environmental & Mathematical Sciences, 2017, University of New South Wales

 Despite tremendous progress in modern medicine in the last century and the successful obliteration of many diseases, there are still many diseases challenging human health,… (more)

Subjects/Keywords: anti-parasitic properties of oligonuclear ruthenium(II) complexes; oligonuclear ruthenium(II) complexes; acetylcholinesterase enzyme inhibitors; phosphatase enzymes (MKPs) enzyme inhibitors

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APA (6th Edition):

Sundaraneedi, M. K. (2017). Targeting enzymes with oligonuclear ruthenium(II) complexes. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/59054 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:48368/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Sundaraneedi, Madhu Kiran. “Targeting enzymes with oligonuclear ruthenium(II) complexes.” 2017. Doctoral Dissertation, University of New South Wales. Accessed April 19, 2021. http://handle.unsw.edu.au/1959.4/59054 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:48368/SOURCE02?view=true.

MLA Handbook (7th Edition):

Sundaraneedi, Madhu Kiran. “Targeting enzymes with oligonuclear ruthenium(II) complexes.” 2017. Web. 19 Apr 2021.

Vancouver:

Sundaraneedi MK. Targeting enzymes with oligonuclear ruthenium(II) complexes. [Internet] [Doctoral dissertation]. University of New South Wales; 2017. [cited 2021 Apr 19]. Available from: http://handle.unsw.edu.au/1959.4/59054 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:48368/SOURCE02?view=true.

Council of Science Editors:

Sundaraneedi MK. Targeting enzymes with oligonuclear ruthenium(II) complexes. [Doctoral Dissertation]. University of New South Wales; 2017. Available from: http://handle.unsw.edu.au/1959.4/59054 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:48368/SOURCE02?view=true

22. Cochrane, Meredith Lee. Inhibition of Cytochrome P450 2C9 by essential oils.

Degree: 2015, NC Docks

 Cytochrome P450 enzymes (CYP450) are the prominent member of a family of xenobiotic metabolizing enzymes that are collectively referred to as Phase 1 enzymes (1).… (more)

Subjects/Keywords: Cytochrome P-450 $x Inhibitors; Enzyme inhibitors; Essences and essential oils $x Physiological effect

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APA (6th Edition):

Cochrane, M. L. (2015). Inhibition of Cytochrome P450 2C9 by essential oils. (Thesis). NC Docks. Retrieved from http://libres.uncg.edu/ir/uncg/f/Cochrane_uncg_0154M_11712.pdf

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):

Cochrane, Meredith Lee. “Inhibition of Cytochrome P450 2C9 by essential oils.” 2015. Thesis, NC Docks. Accessed April 19, 2021. http://libres.uncg.edu/ir/uncg/f/Cochrane_uncg_0154M_11712.pdf.

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

MLA Handbook (7th Edition):

Cochrane, Meredith Lee. “Inhibition of Cytochrome P450 2C9 by essential oils.” 2015. Web. 19 Apr 2021.

Vancouver:

Cochrane ML. Inhibition of Cytochrome P450 2C9 by essential oils. [Internet] [Thesis]. NC Docks; 2015. [cited 2021 Apr 19]. Available from: http://libres.uncg.edu/ir/uncg/f/Cochrane_uncg_0154M_11712.pdf.

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

Council of Science Editors:

Cochrane ML. Inhibition of Cytochrome P450 2C9 by essential oils. [Thesis]. NC Docks; 2015. Available from: http://libres.uncg.edu/ir/uncg/f/Cochrane_uncg_0154M_11712.pdf

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


Macquarie University

23. Smith, Jason R. Indoleamine 2,3-dioxygenase 1: mapping the active site and discovery of novel inhibitors.

Degree: 2012, Macquarie University

"A thesis submitted in the partial fulfillment of the requirements for the award of the degree of Master of Philosophy."

1. Introduction  – 2. Selection… (more)

Subjects/Keywords: Heme oxygenase; Enzyme inhibitors; Indoleamine 2,3-dioxygenase-1; heme oxygenase; enzyme inhabitors

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APA (6th Edition):

Smith, J. R. (2012). Indoleamine 2,3-dioxygenase 1: mapping the active site and discovery of novel inhibitors. (Masters Thesis). Macquarie University. Retrieved from http://hdl.handle.net/1959.14/1138188

Chicago Manual of Style (16th Edition):

Smith, Jason R. “Indoleamine 2,3-dioxygenase 1: mapping the active site and discovery of novel inhibitors.” 2012. Masters Thesis, Macquarie University. Accessed April 19, 2021. http://hdl.handle.net/1959.14/1138188.

MLA Handbook (7th Edition):

Smith, Jason R. “Indoleamine 2,3-dioxygenase 1: mapping the active site and discovery of novel inhibitors.” 2012. Web. 19 Apr 2021.

Vancouver:

Smith JR. Indoleamine 2,3-dioxygenase 1: mapping the active site and discovery of novel inhibitors. [Internet] [Masters thesis]. Macquarie University; 2012. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/1959.14/1138188.

Council of Science Editors:

Smith JR. Indoleamine 2,3-dioxygenase 1: mapping the active site and discovery of novel inhibitors. [Masters Thesis]. Macquarie University; 2012. Available from: http://hdl.handle.net/1959.14/1138188


University of New South Wales

24. Suharto, Adrian Rinaldi. Structural studies of giardial arginine deiminase.

Degree: Biotechnology and Biomolecular Sciences, 2006, University of New South Wales

 Recombinant giardial arginine deiminase (rADI) was characterized. The enzyme was found to have a specific activity of 12 U (mg protein)-1under at pH 7.4 and… (more)

Subjects/Keywords: Enzyme inhibitors; Enzyme kinetics; Giardia lamblia

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APA (6th Edition):

Suharto, A. R. (2006). Structural studies of giardial arginine deiminase. (Masters Thesis). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/26293 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:1153/SOURCE1?view=true

Chicago Manual of Style (16th Edition):

Suharto, Adrian Rinaldi. “Structural studies of giardial arginine deiminase.” 2006. Masters Thesis, University of New South Wales. Accessed April 19, 2021. http://handle.unsw.edu.au/1959.4/26293 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:1153/SOURCE1?view=true.

MLA Handbook (7th Edition):

Suharto, Adrian Rinaldi. “Structural studies of giardial arginine deiminase.” 2006. Web. 19 Apr 2021.

Vancouver:

Suharto AR. Structural studies of giardial arginine deiminase. [Internet] [Masters thesis]. University of New South Wales; 2006. [cited 2021 Apr 19]. Available from: http://handle.unsw.edu.au/1959.4/26293 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:1153/SOURCE1?view=true.

Council of Science Editors:

Suharto AR. Structural studies of giardial arginine deiminase. [Masters Thesis]. University of New South Wales; 2006. Available from: http://handle.unsw.edu.au/1959.4/26293 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:1153/SOURCE1?view=true


Nelson Mandela Metropolitan University

25. Chada, Sravanthi. A new synthetic approach for preparation of efavirenz.

Degree: Faculty of Science, 2017, Nelson Mandela Metropolitan University

 Efavirenz, a drug that is still inaccessible to millions of people worldwide, is potent non nucleoside reverse transcriptase inhibitor (NNRTI), is one of the preferred… (more)

Subjects/Keywords: Asymmetric synthesis; Antiretroviral agents; Enzyme inhibitors; HIV (Viruses)  – Enzymes

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APA (6th Edition):

Chada, S. (2017). A new synthetic approach for preparation of efavirenz. (Thesis). Nelson Mandela Metropolitan University. Retrieved from http://hdl.handle.net/10948/15512

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):

Chada, Sravanthi. “A new synthetic approach for preparation of efavirenz.” 2017. Thesis, Nelson Mandela Metropolitan University. Accessed April 19, 2021. http://hdl.handle.net/10948/15512.

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

MLA Handbook (7th Edition):

Chada, Sravanthi. “A new synthetic approach for preparation of efavirenz.” 2017. Web. 19 Apr 2021.

Vancouver:

Chada S. A new synthetic approach for preparation of efavirenz. [Internet] [Thesis]. Nelson Mandela Metropolitan University; 2017. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/10948/15512.

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

Council of Science Editors:

Chada S. A new synthetic approach for preparation of efavirenz. [Thesis]. Nelson Mandela Metropolitan University; 2017. Available from: http://hdl.handle.net/10948/15512

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


Loyola University Chicago

26. Heath, Tahirah. The Enzymatic Activity and Inhibition of DapE Encoded N-Succinyl-L,l-Diaminopimelic Acid Dessucinylase.

Degree: PhD, Chemistry, 2018, Loyola University Chicago

  The bacterial enzyme DapE is a hydrolase in the late stage of the mDAP/lysine biosynthetic pathway that catalyzes the hydrolysis of N-succinyl-L,L-diaminopimelic acid (L,L-SDAP)… (more)

Subjects/Keywords: Assay; DapE; Enzyme; Indolines; Inhibitors; ninhydrin; Organic Chemistry

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APA (6th Edition):

Heath, T. (2018). The Enzymatic Activity and Inhibition of DapE Encoded N-Succinyl-L,l-Diaminopimelic Acid Dessucinylase. (Doctoral Dissertation). Loyola University Chicago. Retrieved from https://ecommons.luc.edu/luc_diss/2811

Chicago Manual of Style (16th Edition):

Heath, Tahirah. “The Enzymatic Activity and Inhibition of DapE Encoded N-Succinyl-L,l-Diaminopimelic Acid Dessucinylase.” 2018. Doctoral Dissertation, Loyola University Chicago. Accessed April 19, 2021. https://ecommons.luc.edu/luc_diss/2811.

MLA Handbook (7th Edition):

Heath, Tahirah. “The Enzymatic Activity and Inhibition of DapE Encoded N-Succinyl-L,l-Diaminopimelic Acid Dessucinylase.” 2018. Web. 19 Apr 2021.

Vancouver:

Heath T. The Enzymatic Activity and Inhibition of DapE Encoded N-Succinyl-L,l-Diaminopimelic Acid Dessucinylase. [Internet] [Doctoral dissertation]. Loyola University Chicago; 2018. [cited 2021 Apr 19]. Available from: https://ecommons.luc.edu/luc_diss/2811.

Council of Science Editors:

Heath T. The Enzymatic Activity and Inhibition of DapE Encoded N-Succinyl-L,l-Diaminopimelic Acid Dessucinylase. [Doctoral Dissertation]. Loyola University Chicago; 2018. Available from: https://ecommons.luc.edu/luc_diss/2811

27. Matongo, Fredrick. Inhibitory potential of honey on the enzymatic activity of helicobacter pylori urease.

Degree: Faculty of Science and Agriculture, 2012, University of Fort Hare

 Urease of Helicobacter pylori is an important virulence factor implicated in the pathogenesis of many clinical conditions, such as chronic gastritis, peptic ulceration, and gastric… (more)

Subjects/Keywords: Honey; Helicobacter pylori infections; Enzyme inhibitors; Traditional medicine; Antifungal agents

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APA (6th Edition):

Matongo, F. (2012). Inhibitory potential of honey on the enzymatic activity of helicobacter pylori urease. (Thesis). University of Fort Hare. Retrieved from http://hdl.handle.net/10353/431

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):

Matongo, Fredrick. “Inhibitory potential of honey on the enzymatic activity of helicobacter pylori urease.” 2012. Thesis, University of Fort Hare. Accessed April 19, 2021. http://hdl.handle.net/10353/431.

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

MLA Handbook (7th Edition):

Matongo, Fredrick. “Inhibitory potential of honey on the enzymatic activity of helicobacter pylori urease.” 2012. Web. 19 Apr 2021.

Vancouver:

Matongo F. Inhibitory potential of honey on the enzymatic activity of helicobacter pylori urease. [Internet] [Thesis]. University of Fort Hare; 2012. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/10353/431.

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

Council of Science Editors:

Matongo F. Inhibitory potential of honey on the enzymatic activity of helicobacter pylori urease. [Thesis]. University of Fort Hare; 2012. Available from: http://hdl.handle.net/10353/431

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

28. Tanner, Carol. Biochemical and Microbiological Investigations of Inhibitors for β-Lactamases from Human Pathogenic Bacteria.

Degree: 2019, University of Waterloo

 The majority of antibiotics prescribed for treatment of bacterial infections are β-lactam antibiotics. Resistance to these has evolved in a few different ways, notably by… (more)

Subjects/Keywords: β-lactamases; β-lactamase inhibitors; enzyme kinetics; antibiotics; cephalosporin

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APA (6th Edition):

Tanner, C. (2019). Biochemical and Microbiological Investigations of Inhibitors for β-Lactamases from Human Pathogenic Bacteria. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/14601

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):

Tanner, Carol. “Biochemical and Microbiological Investigations of Inhibitors for β-Lactamases from Human Pathogenic Bacteria.” 2019. Thesis, University of Waterloo. Accessed April 19, 2021. http://hdl.handle.net/10012/14601.

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

MLA Handbook (7th Edition):

Tanner, Carol. “Biochemical and Microbiological Investigations of Inhibitors for β-Lactamases from Human Pathogenic Bacteria.” 2019. Web. 19 Apr 2021.

Vancouver:

Tanner C. Biochemical and Microbiological Investigations of Inhibitors for β-Lactamases from Human Pathogenic Bacteria. [Internet] [Thesis]. University of Waterloo; 2019. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/10012/14601.

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

Council of Science Editors:

Tanner C. Biochemical and Microbiological Investigations of Inhibitors for β-Lactamases from Human Pathogenic Bacteria. [Thesis]. University of Waterloo; 2019. Available from: http://hdl.handle.net/10012/14601

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


University of Texas Southwestern Medical Center

29. Kulak, Ozlem. Chemical Disruption of Wnt Signaling and Telomere Length Maintenance.

Degree: 2015, University of Texas Southwestern Medical Center

Pages xvii-xviii of the dissertation are incorrectly numbered as pages xvi-xvii.

A nearly universal feature of colorectal cancer (CRC) incidents is the presence of genetic… (more)

Subjects/Keywords: Enzyme Inhibitors; Tankyrases; Telomere Shortening; Wnt Signaling Pathway

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

APA (6th Edition):

Kulak, O. (2015). Chemical Disruption of Wnt Signaling and Telomere Length Maintenance. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4110

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):

Kulak, Ozlem. “Chemical Disruption of Wnt Signaling and Telomere Length Maintenance.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed April 19, 2021. http://hdl.handle.net/2152.5/4110.

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

MLA Handbook (7th Edition):

Kulak, Ozlem. “Chemical Disruption of Wnt Signaling and Telomere Length Maintenance.” 2015. Web. 19 Apr 2021.

Vancouver:

Kulak O. Chemical Disruption of Wnt Signaling and Telomere Length Maintenance. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/2152.5/4110.

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

Council of Science Editors:

Kulak O. Chemical Disruption of Wnt Signaling and Telomere Length Maintenance. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4110

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


University of Waterloo

30. Estavillo, Danica. In vitro studies of NOS inhibitors using purified human NOS isozymes.

Degree: 2017, University of Waterloo

 Endogenous nitric oxide (NO) is derived from L-arginine via a chemical reaction catalyzed by nitric oxide synthases (NOS). Three NOS isozymes are found in humans:… (more)

Subjects/Keywords: nitric oxide; nitric oxide synthase; NOS inhibitors; enzyme kinetics

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

APA (6th Edition):

Estavillo, D. (2017). In vitro studies of NOS inhibitors using purified human NOS isozymes. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/12744

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):

Estavillo, Danica. “In vitro studies of NOS inhibitors using purified human NOS isozymes.” 2017. Thesis, University of Waterloo. Accessed April 19, 2021. http://hdl.handle.net/10012/12744.

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

MLA Handbook (7th Edition):

Estavillo, Danica. “In vitro studies of NOS inhibitors using purified human NOS isozymes.” 2017. Web. 19 Apr 2021.

Vancouver:

Estavillo D. In vitro studies of NOS inhibitors using purified human NOS isozymes. [Internet] [Thesis]. University of Waterloo; 2017. [cited 2021 Apr 19]. Available from: http://hdl.handle.net/10012/12744.

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

Council of Science Editors:

Estavillo D. In vitro studies of NOS inhibitors using purified human NOS isozymes. [Thesis]. University of Waterloo; 2017. Available from: http://hdl.handle.net/10012/12744

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

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