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You searched for subject:(Cysteine proteinases Inhibitors). Showing records 1 – 17 of 17 total matches.

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Rhodes University

1. Kroon, Matthys Christoffel. High-throughput modelling and structural investigation of cysteine protease complexes with protein inhibitors.

Degree: Faculty of Science, Biochemistry, Microbiology and Biotechnology, 2013, Rhodes University

 The papain-like cysteine protease family (C1 proteases) is highly important because of its involvement in research and industrial applications and its role in various human… (more)

Subjects/Keywords: Cysteine proteinases; Cysteine proteinases  – Inhibitors; Papain; Cystatins; Malaria  – Chemotherapy; Homology (Biology); Protein-protein interactions

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APA (6th Edition):

Kroon, M. C. (2013). High-throughput modelling and structural investigation of cysteine protease complexes with protein inhibitors. (Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1001619

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):

Kroon, Matthys Christoffel. “High-throughput modelling and structural investigation of cysteine protease complexes with protein inhibitors.” 2013. Thesis, Rhodes University. Accessed March 06, 2021. http://hdl.handle.net/10962/d1001619.

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

MLA Handbook (7th Edition):

Kroon, Matthys Christoffel. “High-throughput modelling and structural investigation of cysteine protease complexes with protein inhibitors.” 2013. Web. 06 Mar 2021.

Vancouver:

Kroon MC. High-throughput modelling and structural investigation of cysteine protease complexes with protein inhibitors. [Internet] [Thesis]. Rhodes University; 2013. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/10962/d1001619.

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

Council of Science Editors:

Kroon MC. High-throughput modelling and structural investigation of cysteine protease complexes with protein inhibitors. [Thesis]. Rhodes University; 2013. Available from: http://hdl.handle.net/10962/d1001619

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


University of Alberta

2. Miyyapuram, Venugopal. Synthesis and investigation of viral cysteine protease inhibitors and biosynthetic studies on subtilosin A.

Degree: PhD, Department of Chemistry, 2009, University of Alberta

 ABSTRACT This thesis discusses the synthesis and evaluation of cysteine protease inhibitors, the asymmetric reduction of pseudoxazolones, and the study of the mechanism of subtilosin… (more)

Subjects/Keywords: Cyclic peptides  – Synthesis; Peptide antibiotics  – Synthesis; Cysteine proteinases  – Inhibitors  – Synthesis; Cysteine proteinases  – Inhibitors  – Evaluation; Bacillus subtilis  – Genetics; SARS (Disease)  – Chemotherapy

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APA (6th Edition):

Miyyapuram, V. (2009). Synthesis and investigation of viral cysteine protease inhibitors and biosynthetic studies on subtilosin A. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/44558f540

Chicago Manual of Style (16th Edition):

Miyyapuram, Venugopal. “Synthesis and investigation of viral cysteine protease inhibitors and biosynthetic studies on subtilosin A.” 2009. Doctoral Dissertation, University of Alberta. Accessed March 06, 2021. https://era.library.ualberta.ca/files/44558f540.

MLA Handbook (7th Edition):

Miyyapuram, Venugopal. “Synthesis and investigation of viral cysteine protease inhibitors and biosynthetic studies on subtilosin A.” 2009. Web. 06 Mar 2021.

Vancouver:

Miyyapuram V. Synthesis and investigation of viral cysteine protease inhibitors and biosynthetic studies on subtilosin A. [Internet] [Doctoral dissertation]. University of Alberta; 2009. [cited 2021 Mar 06]. Available from: https://era.library.ualberta.ca/files/44558f540.

Council of Science Editors:

Miyyapuram V. Synthesis and investigation of viral cysteine protease inhibitors and biosynthetic studies on subtilosin A. [Doctoral Dissertation]. University of Alberta; 2009. Available from: https://era.library.ualberta.ca/files/44558f540


Georgia Tech

3. Rukamp, Brian John. Design, synthesis, and evaluation of novel thiobenzyl ester substrates and aza-peptide inhibitors for serine and cysteine proteases.

Degree: PhD, Chemistry and Biochemistry, 2003, Georgia Tech

Subjects/Keywords: Protease inhibitors; Serine proteinases; Cysteine proteinases; Serine proteinases; Protease inhibitors; Cysteine proteinases

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APA (6th Edition):

Rukamp, B. J. (2003). Design, synthesis, and evaluation of novel thiobenzyl ester substrates and aza-peptide inhibitors for serine and cysteine proteases. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/5371

Chicago Manual of Style (16th Edition):

Rukamp, Brian John. “Design, synthesis, and evaluation of novel thiobenzyl ester substrates and aza-peptide inhibitors for serine and cysteine proteases.” 2003. Doctoral Dissertation, Georgia Tech. Accessed March 06, 2021. http://hdl.handle.net/1853/5371.

MLA Handbook (7th Edition):

Rukamp, Brian John. “Design, synthesis, and evaluation of novel thiobenzyl ester substrates and aza-peptide inhibitors for serine and cysteine proteases.” 2003. Web. 06 Mar 2021.

Vancouver:

Rukamp BJ. Design, synthesis, and evaluation of novel thiobenzyl ester substrates and aza-peptide inhibitors for serine and cysteine proteases. [Internet] [Doctoral dissertation]. Georgia Tech; 2003. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1853/5371.

Council of Science Editors:

Rukamp BJ. Design, synthesis, and evaluation of novel thiobenzyl ester substrates and aza-peptide inhibitors for serine and cysteine proteases. [Doctoral Dissertation]. Georgia Tech; 2003. Available from: http://hdl.handle.net/1853/5371


Georgia Tech

4. Rukamp, Karrie Eileen Adlington. Design and synthesis of inhibitors for serine and cysteine proteases.

Degree: PhD, Chemistry and Biochemistry, 2003, Georgia Tech

Subjects/Keywords: Protease inhibitors; Serine proteinases; Cysteine proteinases; Serine proteinases; Protease inhibitors; Cysteine proteinases

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APA (6th Edition):

Rukamp, K. E. A. (2003). Design and synthesis of inhibitors for serine and cysteine proteases. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/5426

Chicago Manual of Style (16th Edition):

Rukamp, Karrie Eileen Adlington. “Design and synthesis of inhibitors for serine and cysteine proteases.” 2003. Doctoral Dissertation, Georgia Tech. Accessed March 06, 2021. http://hdl.handle.net/1853/5426.

MLA Handbook (7th Edition):

Rukamp, Karrie Eileen Adlington. “Design and synthesis of inhibitors for serine and cysteine proteases.” 2003. Web. 06 Mar 2021.

Vancouver:

Rukamp KEA. Design and synthesis of inhibitors for serine and cysteine proteases. [Internet] [Doctoral dissertation]. Georgia Tech; 2003. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1853/5426.

Council of Science Editors:

Rukamp KEA. Design and synthesis of inhibitors for serine and cysteine proteases. [Doctoral Dissertation]. Georgia Tech; 2003. Available from: http://hdl.handle.net/1853/5426


University of Johannesburg

5. Bester, Christell. Detection of a papaya cysteine proteinase inhibitor under different environmental conditions.

Degree: 2012, University of Johannesburg

M.Sc.

Proteinases are involved in many cellular reactions involving protein degradation, such as degradation of storage proteins and protein degradation during senescence processes. Their action… (more)

Subjects/Keywords: Cysteine proteinases  – Research; Protease inhibitors  – Research; Proteinase  – Inhibitors  – Research; Proteolytic enzymes  – Inhibitors  – Research.; Papaya  – Research

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APA (6th Edition):

Bester, C. (2012). Detection of a papaya cysteine proteinase inhibitor under different environmental conditions. (Thesis). University of Johannesburg. Retrieved from http://hdl.handle.net/10210/6145

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):

Bester, Christell. “Detection of a papaya cysteine proteinase inhibitor under different environmental conditions.” 2012. Thesis, University of Johannesburg. Accessed March 06, 2021. http://hdl.handle.net/10210/6145.

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

MLA Handbook (7th Edition):

Bester, Christell. “Detection of a papaya cysteine proteinase inhibitor under different environmental conditions.” 2012. Web. 06 Mar 2021.

Vancouver:

Bester C. Detection of a papaya cysteine proteinase inhibitor under different environmental conditions. [Internet] [Thesis]. University of Johannesburg; 2012. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/10210/6145.

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

Council of Science Editors:

Bester C. Detection of a papaya cysteine proteinase inhibitor under different environmental conditions. [Thesis]. University of Johannesburg; 2012. Available from: http://hdl.handle.net/10210/6145

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


Georgia Tech

6. Bridges, Sylvia Shadinger. Design, synthesis, and evaluation of cysteine protease inhibitors.

Degree: PhD, Chemistry and Biochemistry, 2008, Georgia Tech

 Proteases are enzymes that cleave protein amide bonds. Proteases are involved in a myriad of biological processes and are considered good targets for drug design.… (more)

Subjects/Keywords: Clostripain; Proteinase; Cysteine proteinases Inhibitors

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APA (6th Edition):

Bridges, S. S. (2008). Design, synthesis, and evaluation of cysteine protease inhibitors. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/29738

Chicago Manual of Style (16th Edition):

Bridges, Sylvia Shadinger. “Design, synthesis, and evaluation of cysteine protease inhibitors.” 2008. Doctoral Dissertation, Georgia Tech. Accessed March 06, 2021. http://hdl.handle.net/1853/29738.

MLA Handbook (7th Edition):

Bridges, Sylvia Shadinger. “Design, synthesis, and evaluation of cysteine protease inhibitors.” 2008. Web. 06 Mar 2021.

Vancouver:

Bridges SS. Design, synthesis, and evaluation of cysteine protease inhibitors. [Internet] [Doctoral dissertation]. Georgia Tech; 2008. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1853/29738.

Council of Science Editors:

Bridges SS. Design, synthesis, and evaluation of cysteine protease inhibitors. [Doctoral Dissertation]. Georgia Tech; 2008. Available from: http://hdl.handle.net/1853/29738


Georgia Tech

7. Krauser, Joel Anderson. Design, synthesis and evaluation of novel inhibitors and fluorogenic substrates for cysteine proteases and metallo proteases.

Degree: PhD, Chemistry, 2001, Georgia Tech

Subjects/Keywords: Protease inhibitors; Cysteine proteinases

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APA (6th Edition):

Krauser, J. A. (2001). Design, synthesis and evaluation of novel inhibitors and fluorogenic substrates for cysteine proteases and metallo proteases. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/30003

Chicago Manual of Style (16th Edition):

Krauser, Joel Anderson. “Design, synthesis and evaluation of novel inhibitors and fluorogenic substrates for cysteine proteases and metallo proteases.” 2001. Doctoral Dissertation, Georgia Tech. Accessed March 06, 2021. http://hdl.handle.net/1853/30003.

MLA Handbook (7th Edition):

Krauser, Joel Anderson. “Design, synthesis and evaluation of novel inhibitors and fluorogenic substrates for cysteine proteases and metallo proteases.” 2001. Web. 06 Mar 2021.

Vancouver:

Krauser JA. Design, synthesis and evaluation of novel inhibitors and fluorogenic substrates for cysteine proteases and metallo proteases. [Internet] [Doctoral dissertation]. Georgia Tech; 2001. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1853/30003.

Council of Science Editors:

Krauser JA. Design, synthesis and evaluation of novel inhibitors and fluorogenic substrates for cysteine proteases and metallo proteases. [Doctoral Dissertation]. Georgia Tech; 2001. Available from: http://hdl.handle.net/1853/30003


Rhodes University

8. Kanzi, Aquillah Mumo. Falcipains as malarial drug targets.

Degree: Faculty of Science, Biochemistry, Microbiology and Biotechnology, 2013, Rhodes University

 Malaria is an infectious disease caused by parasites of the Plasmodium genus with mortality rates of more than a million annually, hence a major global… (more)

Subjects/Keywords: Malaria; Malaria  – Chemotherapy; Plasmodium falciparum; Antimalarials  – Development; Cysteine proteinases; Cysteine proteinases  – Inhibitors; Papain; Drug development; Bioinformatics

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APA (6th Edition):

Kanzi, A. M. (2013). Falcipains as malarial drug targets. (Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1003842

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):

Kanzi, Aquillah Mumo. “Falcipains as malarial drug targets.” 2013. Thesis, Rhodes University. Accessed March 06, 2021. http://hdl.handle.net/10962/d1003842.

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

MLA Handbook (7th Edition):

Kanzi, Aquillah Mumo. “Falcipains as malarial drug targets.” 2013. Web. 06 Mar 2021.

Vancouver:

Kanzi AM. Falcipains as malarial drug targets. [Internet] [Thesis]. Rhodes University; 2013. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/10962/d1003842.

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

Council of Science Editors:

Kanzi AM. Falcipains as malarial drug targets. [Thesis]. Rhodes University; 2013. Available from: http://hdl.handle.net/10962/d1003842

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


Georgia Tech

9. Gheura, Iuliana L. Design, synthesis and evaluation of AZA-peptide epoxides as inhibitors of cysteine proteases.

Degree: PhD, Chemistry, 2002, Georgia Tech

Subjects/Keywords: Protease inhibitors; Epoxy compounds; Cysteine proteinases

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APA (6th Edition):

Gheura, I. L. (2002). Design, synthesis and evaluation of AZA-peptide epoxides as inhibitors of cysteine proteases. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/30571

Chicago Manual of Style (16th Edition):

Gheura, Iuliana L. “Design, synthesis and evaluation of AZA-peptide epoxides as inhibitors of cysteine proteases.” 2002. Doctoral Dissertation, Georgia Tech. Accessed March 06, 2021. http://hdl.handle.net/1853/30571.

MLA Handbook (7th Edition):

Gheura, Iuliana L. “Design, synthesis and evaluation of AZA-peptide epoxides as inhibitors of cysteine proteases.” 2002. Web. 06 Mar 2021.

Vancouver:

Gheura IL. Design, synthesis and evaluation of AZA-peptide epoxides as inhibitors of cysteine proteases. [Internet] [Doctoral dissertation]. Georgia Tech; 2002. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1853/30571.

Council of Science Editors:

Gheura IL. Design, synthesis and evaluation of AZA-peptide epoxides as inhibitors of cysteine proteases. [Doctoral Dissertation]. Georgia Tech; 2002. Available from: http://hdl.handle.net/1853/30571


Michigan State University

10. Babiker, Abdalla Sidahmed Mohammed. Endogenous proteinases and postmortem proteolysis in rabbit longissimus muscle.

Degree: PhD, Department of Animal Science, 1989, Michigan State University

Subjects/Keywords: Proteinase; Enzyme inhibitors; Cysteine proteinases – Inhibitors; Rabbits; Meat

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APA (6th Edition):

Babiker, A. S. M. (1989). Endogenous proteinases and postmortem proteolysis in rabbit longissimus muscle. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:29022

Chicago Manual of Style (16th Edition):

Babiker, Abdalla Sidahmed Mohammed. “Endogenous proteinases and postmortem proteolysis in rabbit longissimus muscle.” 1989. Doctoral Dissertation, Michigan State University. Accessed March 06, 2021. http://etd.lib.msu.edu/islandora/object/etd:29022.

MLA Handbook (7th Edition):

Babiker, Abdalla Sidahmed Mohammed. “Endogenous proteinases and postmortem proteolysis in rabbit longissimus muscle.” 1989. Web. 06 Mar 2021.

Vancouver:

Babiker ASM. Endogenous proteinases and postmortem proteolysis in rabbit longissimus muscle. [Internet] [Doctoral dissertation]. Michigan State University; 1989. [cited 2021 Mar 06]. Available from: http://etd.lib.msu.edu/islandora/object/etd:29022.

Council of Science Editors:

Babiker ASM. Endogenous proteinases and postmortem proteolysis in rabbit longissimus muscle. [Doctoral Dissertation]. Michigan State University; 1989. Available from: http://etd.lib.msu.edu/islandora/object/etd:29022

11. Ovat, Asli. Design, synthesis and evaluation of cysteine protease inhibitors.

Degree: PhD, Chemistry and Biochemistry, 2009, Georgia Tech

Cysteine proteases are important drug targets due to their involvement in many biological processes such as protein turnover, digestion, blood coagulation, apoptosis, cell differentiation, cell… (more)

Subjects/Keywords: Legumain; Calpain; Protease; Cysteine; Cysteine proteinases; Cysteine proteinases Inhibitors; Protease inhibitors; Biosynthesis; Epoxy compounds

cysteine proteases since the inhibitors reported in this thesis are designed for the enzymes… …thesis are competitive inhibitors of cysteine proteases since they are competing with the… …vinyl sulfone inhibitors of cysteine proteases demonstrated that introduction of the… …Subsites 2 Figure 1.3: Substrate Hydrolysis Mechanism of Cysteine Proteases 4 Figure 2.1… …Endopeptidases 28 Figure 2.12: Mechanism of Inhibition of Cysteine Proteases by Michael Acceptor and… 

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APA (6th Edition):

Ovat, A. (2009). Design, synthesis and evaluation of cysteine protease inhibitors. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/33822

Chicago Manual of Style (16th Edition):

Ovat, Asli. “Design, synthesis and evaluation of cysteine protease inhibitors.” 2009. Doctoral Dissertation, Georgia Tech. Accessed March 06, 2021. http://hdl.handle.net/1853/33822.

MLA Handbook (7th Edition):

Ovat, Asli. “Design, synthesis and evaluation of cysteine protease inhibitors.” 2009. Web. 06 Mar 2021.

Vancouver:

Ovat A. Design, synthesis and evaluation of cysteine protease inhibitors. [Internet] [Doctoral dissertation]. Georgia Tech; 2009. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1853/33822.

Council of Science Editors:

Ovat A. Design, synthesis and evaluation of cysteine protease inhibitors. [Doctoral Dissertation]. Georgia Tech; 2009. Available from: http://hdl.handle.net/1853/33822


University of Hong Kong

12. Ma, Ka-li, Marcella. Epigenetic regulation of gene expression of cystatin 6, CST6, in hepatocellular carcinoma.

Degree: 2005, University of Hong Kong

Subjects/Keywords: Genetic regulation.; Antioncogenes.; Cysteine proteinases - Inhibitors.; Liver - Cancer - Genetic aspects.

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APA (6th Edition):

Ma, Ka-li, M. (2005). Epigenetic regulation of gene expression of cystatin 6, CST6, in hepatocellular carcinoma. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/131220

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):

Ma, Ka-li, Marcella. “Epigenetic regulation of gene expression of cystatin 6, CST6, in hepatocellular carcinoma.” 2005. Thesis, University of Hong Kong. Accessed March 06, 2021. http://hdl.handle.net/10722/131220.

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

MLA Handbook (7th Edition):

Ma, Ka-li, Marcella. “Epigenetic regulation of gene expression of cystatin 6, CST6, in hepatocellular carcinoma.” 2005. Web. 06 Mar 2021.

Vancouver:

Ma, Ka-li M. Epigenetic regulation of gene expression of cystatin 6, CST6, in hepatocellular carcinoma. [Internet] [Thesis]. University of Hong Kong; 2005. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/10722/131220.

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

Council of Science Editors:

Ma, Ka-li M. Epigenetic regulation of gene expression of cystatin 6, CST6, in hepatocellular carcinoma. [Thesis]. University of Hong Kong; 2005. Available from: http://hdl.handle.net/10722/131220

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


Baylor University

13. Arispe Angulo, Wara Milenka. Inhibitors of human cathepsin L and cruzain as therapeutic agents.

Degree: PhD, Chemistry and Biochemistry., 2009, Baylor University

 Increased human cathepsin L activity is linked to invasive and metastatic cancers where it promotes degradation of the extracellular matrix. This major cysteine protease found… (more)

Subjects/Keywords: Protease inhibitors.; Cysteine proteinases  – Testing.; Cancer  – Treatment.; Chagas' disease  – Treatment.

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APA (6th Edition):

Arispe Angulo, W. M. (2009). Inhibitors of human cathepsin L and cruzain as therapeutic agents. (Doctoral Dissertation). Baylor University. Retrieved from http://hdl.handle.net/2104/5290

Chicago Manual of Style (16th Edition):

Arispe Angulo, Wara Milenka. “Inhibitors of human cathepsin L and cruzain as therapeutic agents.” 2009. Doctoral Dissertation, Baylor University. Accessed March 06, 2021. http://hdl.handle.net/2104/5290.

MLA Handbook (7th Edition):

Arispe Angulo, Wara Milenka. “Inhibitors of human cathepsin L and cruzain as therapeutic agents.” 2009. Web. 06 Mar 2021.

Vancouver:

Arispe Angulo WM. Inhibitors of human cathepsin L and cruzain as therapeutic agents. [Internet] [Doctoral dissertation]. Baylor University; 2009. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/2104/5290.

Council of Science Editors:

Arispe Angulo WM. Inhibitors of human cathepsin L and cruzain as therapeutic agents. [Doctoral Dissertation]. Baylor University; 2009. Available from: http://hdl.handle.net/2104/5290


Rutgers University

14. Gomez, Salvador, 1986-. The effects of Cys to Ser substitutions in OxyR on the response of E. coli to stress induced by copper (II) sulfate, diamide, hydrochloric acid, hydrogen peroxide, kanamycin, and methyl viologen dichloride.

Degree: MS, Biology, 2011, Rutgers University

 OxyR is a redox-sensitive transcriptional regulator that activates the expression of defense genes responsible for an oxidative stress response in Escherichia coli. The transcription factor… (more)

Subjects/Keywords: Escherichia coli; Escherichia coli – Genetics; Stress (Physiology); Cysteine proteinases – Inhibitors

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APA (6th Edition):

Gomez, Salvador, 1. (2011). The effects of Cys to Ser substitutions in OxyR on the response of E. coli to stress induced by copper (II) sulfate, diamide, hydrochloric acid, hydrogen peroxide, kanamycin, and methyl viologen dichloride. (Masters Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10005600001.ETD.000057451

Chicago Manual of Style (16th Edition):

Gomez, Salvador, 1986-. “The effects of Cys to Ser substitutions in OxyR on the response of E. coli to stress induced by copper (II) sulfate, diamide, hydrochloric acid, hydrogen peroxide, kanamycin, and methyl viologen dichloride.” 2011. Masters Thesis, Rutgers University. Accessed March 06, 2021. http://hdl.rutgers.edu/1782.1/rucore10005600001.ETD.000057451.

MLA Handbook (7th Edition):

Gomez, Salvador, 1986-. “The effects of Cys to Ser substitutions in OxyR on the response of E. coli to stress induced by copper (II) sulfate, diamide, hydrochloric acid, hydrogen peroxide, kanamycin, and methyl viologen dichloride.” 2011. Web. 06 Mar 2021.

Vancouver:

Gomez, Salvador 1. The effects of Cys to Ser substitutions in OxyR on the response of E. coli to stress induced by copper (II) sulfate, diamide, hydrochloric acid, hydrogen peroxide, kanamycin, and methyl viologen dichloride. [Internet] [Masters thesis]. Rutgers University; 2011. [cited 2021 Mar 06]. Available from: http://hdl.rutgers.edu/1782.1/rucore10005600001.ETD.000057451.

Council of Science Editors:

Gomez, Salvador 1. The effects of Cys to Ser substitutions in OxyR on the response of E. coli to stress induced by copper (II) sulfate, diamide, hydrochloric acid, hydrogen peroxide, kanamycin, and methyl viologen dichloride. [Masters Thesis]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10005600001.ETD.000057451


Georgia Tech

15. Gotz, Marion Gabriele. Design, synthesis, and evaluation of irreversible peptidyl inhibitors for clan CA and clan CD cysteine proteases.

Degree: PhD, Chemistry and Biochemistry, 2004, Georgia Tech

Cysteine proteases are a class of proteolytic enzymes, which are involved in a series of metabolic and catabolic processes, such as protein turnover, digestion, blood… (more)

Subjects/Keywords: Allyl sulfone; Aza-peptide; Biosynthesis; Cysteine protease; Cysteine proteinases; Irreversible inhibitors; Protease inhibitors; Sulphones; Vinyl sulfone

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APA (6th Edition):

Gotz, M. G. (2004). Design, synthesis, and evaluation of irreversible peptidyl inhibitors for clan CA and clan CD cysteine proteases. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/8072

Chicago Manual of Style (16th Edition):

Gotz, Marion Gabriele. “Design, synthesis, and evaluation of irreversible peptidyl inhibitors for clan CA and clan CD cysteine proteases.” 2004. Doctoral Dissertation, Georgia Tech. Accessed March 06, 2021. http://hdl.handle.net/1853/8072.

MLA Handbook (7th Edition):

Gotz, Marion Gabriele. “Design, synthesis, and evaluation of irreversible peptidyl inhibitors for clan CA and clan CD cysteine proteases.” 2004. Web. 06 Mar 2021.

Vancouver:

Gotz MG. Design, synthesis, and evaluation of irreversible peptidyl inhibitors for clan CA and clan CD cysteine proteases. [Internet] [Doctoral dissertation]. Georgia Tech; 2004. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1853/8072.

Council of Science Editors:

Gotz MG. Design, synthesis, and evaluation of irreversible peptidyl inhibitors for clan CA and clan CD cysteine proteases. [Doctoral Dissertation]. Georgia Tech; 2004. Available from: http://hdl.handle.net/1853/8072


IUPUI

16. Guzman, Javier Rivera. THE INHIBITOR-OF-APOPTOSIS PROTEIN SURVIVIN INCREASES P34CDC2 PHOSPHORYLATION AND ENHANCES CELL SURVIVAL AND PROLIFERATION BY PROTECTING THE WEE1 KINASE FROM DEGRADATION BY CASPASE-3.

Degree: 2009, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

The anti-apoptotic protein Survivin and the cyclin-dependent kinase p34Cdc2 are involved in cell cycle progression and apoptosis. Activation of Cdc2… (more)

Subjects/Keywords: p34Cdc2, Survivin, Wee1, Caspase-3, Apoptosis; Cell cycle; Apoptosis  – Prevention; Cysteine proteinases  – Inhibitors; Phosphorylation

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

APA (6th Edition):

Guzman, J. R. (2009). THE INHIBITOR-OF-APOPTOSIS PROTEIN SURVIVIN INCREASES P34CDC2 PHOSPHORYLATION AND ENHANCES CELL SURVIVAL AND PROLIFERATION BY PROTECTING THE WEE1 KINASE FROM DEGRADATION BY CASPASE-3. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/1952

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):

Guzman, Javier Rivera. “THE INHIBITOR-OF-APOPTOSIS PROTEIN SURVIVIN INCREASES P34CDC2 PHOSPHORYLATION AND ENHANCES CELL SURVIVAL AND PROLIFERATION BY PROTECTING THE WEE1 KINASE FROM DEGRADATION BY CASPASE-3.” 2009. Thesis, IUPUI. Accessed March 06, 2021. http://hdl.handle.net/1805/1952.

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

MLA Handbook (7th Edition):

Guzman, Javier Rivera. “THE INHIBITOR-OF-APOPTOSIS PROTEIN SURVIVIN INCREASES P34CDC2 PHOSPHORYLATION AND ENHANCES CELL SURVIVAL AND PROLIFERATION BY PROTECTING THE WEE1 KINASE FROM DEGRADATION BY CASPASE-3.” 2009. Web. 06 Mar 2021.

Vancouver:

Guzman JR. THE INHIBITOR-OF-APOPTOSIS PROTEIN SURVIVIN INCREASES P34CDC2 PHOSPHORYLATION AND ENHANCES CELL SURVIVAL AND PROLIFERATION BY PROTECTING THE WEE1 KINASE FROM DEGRADATION BY CASPASE-3. [Internet] [Thesis]. IUPUI; 2009. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1805/1952.

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

Council of Science Editors:

Guzman JR. THE INHIBITOR-OF-APOPTOSIS PROTEIN SURVIVIN INCREASES P34CDC2 PHOSPHORYLATION AND ENHANCES CELL SURVIVAL AND PROLIFERATION BY PROTECTING THE WEE1 KINASE FROM DEGRADATION BY CASPASE-3. [Thesis]. IUPUI; 2009. Available from: http://hdl.handle.net/1805/1952

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

17. Outchkourov, N.S. Protease inhibitor mediated resistance to insects.

Degree: 2003, NARCIS

 Protease inhibitors (PIs) are among the defensive molecules that plants produce in order to defend themselves against herbivores. A major aim of this thesis is… (more)

Subjects/Keywords: proteïnaseremmers; cysteïne proteïnasen; thrips; thripidae; plaagresistentie; gewasbescherming; transgene planten; waardplanten; Plantenverdediging en -resistentie; Resistentieveredeling; proteinase inhibitors; cysteine proteinases; thrips; thripidae; pest resistance; plant protection; transgenic plants; host plants; Plant Defence, Plant Resistance; Resistance Breeding

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

APA (6th Edition):

Outchkourov, N. S. (2003). Protease inhibitor mediated resistance to insects. (Doctoral Dissertation). NARCIS. Retrieved from http://library.wur.nl/WebQuery/wurpubs/328218 ; urn:nbn:nl:ui:32-328218 ; urn:nbn:nl:ui:32-328218 ; http://library.wur.nl/WebQuery/wurpubs/328218

Chicago Manual of Style (16th Edition):

Outchkourov, N S. “Protease inhibitor mediated resistance to insects.” 2003. Doctoral Dissertation, NARCIS. Accessed March 06, 2021. http://library.wur.nl/WebQuery/wurpubs/328218 ; urn:nbn:nl:ui:32-328218 ; urn:nbn:nl:ui:32-328218 ; http://library.wur.nl/WebQuery/wurpubs/328218.

MLA Handbook (7th Edition):

Outchkourov, N S. “Protease inhibitor mediated resistance to insects.” 2003. Web. 06 Mar 2021.

Vancouver:

Outchkourov NS. Protease inhibitor mediated resistance to insects. [Internet] [Doctoral dissertation]. NARCIS; 2003. [cited 2021 Mar 06]. Available from: http://library.wur.nl/WebQuery/wurpubs/328218 ; urn:nbn:nl:ui:32-328218 ; urn:nbn:nl:ui:32-328218 ; http://library.wur.nl/WebQuery/wurpubs/328218.

Council of Science Editors:

Outchkourov NS. Protease inhibitor mediated resistance to insects. [Doctoral Dissertation]. NARCIS; 2003. Available from: http://library.wur.nl/WebQuery/wurpubs/328218 ; urn:nbn:nl:ui:32-328218 ; urn:nbn:nl:ui:32-328218 ; http://library.wur.nl/WebQuery/wurpubs/328218

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