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You searched for subject:(Protease inhibitors). Showing records 1 – 30 of 182 total matches.

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University of Iceland

1. Sveinn Bjarnason 1990-. Properties of SLPI, a protease inhibitor from Streptomyces lividans and its binding properties to subtilases .

Degree: 2019, University of Iceland

 The goal of this research project was to use isothermal titration calorimetry (ITC) to characterize the binding of a protease inhibitor to the structural homologues… (more)

Subjects/Keywords: Lífefnafræði; Protease inhibitors

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APA (6th Edition):

1990-, S. B. (2019). Properties of SLPI, a protease inhibitor from Streptomyces lividans and its binding properties to subtilases . (Thesis). University of Iceland. Retrieved from http://hdl.handle.net/1946/33305

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):

1990-, Sveinn Bjarnason. “Properties of SLPI, a protease inhibitor from Streptomyces lividans and its binding properties to subtilases .” 2019. Thesis, University of Iceland. Accessed March 06, 2021. http://hdl.handle.net/1946/33305.

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

MLA Handbook (7th Edition):

1990-, Sveinn Bjarnason. “Properties of SLPI, a protease inhibitor from Streptomyces lividans and its binding properties to subtilases .” 2019. Web. 06 Mar 2021.

Vancouver:

1990- SB. Properties of SLPI, a protease inhibitor from Streptomyces lividans and its binding properties to subtilases . [Internet] [Thesis]. University of Iceland; 2019. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1946/33305.

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

Council of Science Editors:

1990- SB. Properties of SLPI, a protease inhibitor from Streptomyces lividans and its binding properties to subtilases . [Thesis]. University of Iceland; 2019. Available from: http://hdl.handle.net/1946/33305

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


Rutgers University

2. Seth Pasricha, Mansha, 1976-. Biochemical and physiological characterization of caspase activity in haloarchaea.

Degree: PhD, Microbiology and Molecular Genetics, 2015, Rutgers University

Caspases, cysteine aspartate-specific proteases, are key initiators and executioners of programmed cell death across a wide array of life. Archaea had been absent from the… (more)

Subjects/Keywords: Catalysts; Protease inhibitors

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APA (6th Edition):

Seth Pasricha, Mansha, 1. (2015). Biochemical and physiological characterization of caspase activity in haloarchaea. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/46431/

Chicago Manual of Style (16th Edition):

Seth Pasricha, Mansha, 1976-. “Biochemical and physiological characterization of caspase activity in haloarchaea.” 2015. Doctoral Dissertation, Rutgers University. Accessed March 06, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/46431/.

MLA Handbook (7th Edition):

Seth Pasricha, Mansha, 1976-. “Biochemical and physiological characterization of caspase activity in haloarchaea.” 2015. Web. 06 Mar 2021.

Vancouver:

Seth Pasricha, Mansha 1. Biochemical and physiological characterization of caspase activity in haloarchaea. [Internet] [Doctoral dissertation]. Rutgers University; 2015. [cited 2021 Mar 06]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/46431/.

Council of Science Editors:

Seth Pasricha, Mansha 1. Biochemical and physiological characterization of caspase activity in haloarchaea. [Doctoral Dissertation]. Rutgers University; 2015. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/46431/

3. Ferreira, Leonardo Luiz Gomes. Estudos das relações quantitativas entre a estrutura e atividade de uma série de inibidores da protease do vírus HIV-1.

Degree: Mestrado, Física Aplicada, 2007, University of São Paulo

A Protease do Vírus da Imunodeficiência Humana Tipo 1 (HIV-1 PR, EC 3.4.23.16) é um alvo macromolecular de grande importância no desenvolvimento de fármacos na… (more)

Subjects/Keywords: HIV; HIV; Inhibitors; Inibidores; Protease; Protease

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APA (6th Edition):

Ferreira, L. L. G. (2007). Estudos das relações quantitativas entre a estrutura e atividade de uma série de inibidores da protease do vírus HIV-1. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/76/76132/tde-17092008-151521/ ;

Chicago Manual of Style (16th Edition):

Ferreira, Leonardo Luiz Gomes. “Estudos das relações quantitativas entre a estrutura e atividade de uma série de inibidores da protease do vírus HIV-1.” 2007. Masters Thesis, University of São Paulo. Accessed March 06, 2021. http://www.teses.usp.br/teses/disponiveis/76/76132/tde-17092008-151521/ ;.

MLA Handbook (7th Edition):

Ferreira, Leonardo Luiz Gomes. “Estudos das relações quantitativas entre a estrutura e atividade de uma série de inibidores da protease do vírus HIV-1.” 2007. Web. 06 Mar 2021.

Vancouver:

Ferreira LLG. Estudos das relações quantitativas entre a estrutura e atividade de uma série de inibidores da protease do vírus HIV-1. [Internet] [Masters thesis]. University of São Paulo; 2007. [cited 2021 Mar 06]. Available from: http://www.teses.usp.br/teses/disponiveis/76/76132/tde-17092008-151521/ ;.

Council of Science Editors:

Ferreira LLG. Estudos das relações quantitativas entre a estrutura e atividade de uma série de inibidores da protease do vírus HIV-1. [Masters Thesis]. University of São Paulo; 2007. Available from: http://www.teses.usp.br/teses/disponiveis/76/76132/tde-17092008-151521/ ;


Michigan State University

4. Giletto, Matthew Basil. The design and synthesis of novel proteasome inhibitors : studies on the synthesis of nagelamide M and analogs, the synthesis of rapamycin based proteasome inhibitors, and the synthesis of TCH based molecular probes for binding site determination.

Degree: 2017, Michigan State University

"The two primary physiologic mechanisms for the recycling of amino acids from no-longer needed or damaged proteins are autophagy and enzymatically via the proteasome. Inhibition… (more)

Subjects/Keywords: Protease inhibitors – Design; Protease inhibitors – Synthesis; Protease inhibitors – Effectiveness; Alkaloids – Synthesis; Rapamycin – Synthesis; Chemistry

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APA (6th Edition):

Giletto, M. B. (2017). The design and synthesis of novel proteasome inhibitors : studies on the synthesis of nagelamide M and analogs, the synthesis of rapamycin based proteasome inhibitors, and the synthesis of TCH based molecular probes for binding site determination. (Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:4596

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):

Giletto, Matthew Basil. “The design and synthesis of novel proteasome inhibitors : studies on the synthesis of nagelamide M and analogs, the synthesis of rapamycin based proteasome inhibitors, and the synthesis of TCH based molecular probes for binding site determination.” 2017. Thesis, Michigan State University. Accessed March 06, 2021. http://etd.lib.msu.edu/islandora/object/etd:4596.

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

MLA Handbook (7th Edition):

Giletto, Matthew Basil. “The design and synthesis of novel proteasome inhibitors : studies on the synthesis of nagelamide M and analogs, the synthesis of rapamycin based proteasome inhibitors, and the synthesis of TCH based molecular probes for binding site determination.” 2017. Web. 06 Mar 2021.

Vancouver:

Giletto MB. The design and synthesis of novel proteasome inhibitors : studies on the synthesis of nagelamide M and analogs, the synthesis of rapamycin based proteasome inhibitors, and the synthesis of TCH based molecular probes for binding site determination. [Internet] [Thesis]. Michigan State University; 2017. [cited 2021 Mar 06]. Available from: http://etd.lib.msu.edu/islandora/object/etd:4596.

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

Council of Science Editors:

Giletto MB. The design and synthesis of novel proteasome inhibitors : studies on the synthesis of nagelamide M and analogs, the synthesis of rapamycin based proteasome inhibitors, and the synthesis of TCH based molecular probes for binding site determination. [Thesis]. Michigan State University; 2017. Available from: http://etd.lib.msu.edu/islandora/object/etd:4596

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


University of Adelaide

5. Schumann, Nicholas. Inhibition of serine and cysteine proteases by peptidomimetic inhibitors.

Degree: 2017, University of Adelaide

 Proteases are responsible for the hydrolysis of proteins and peptides and have been implicated in the development of various diseases. Herein describes the design and… (more)

Subjects/Keywords: Protease; inhibitors; peptidomimetic; serine; cysteine

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APA (6th Edition):

Schumann, N. (2017). Inhibition of serine and cysteine proteases by peptidomimetic inhibitors. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/126464

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):

Schumann, Nicholas. “Inhibition of serine and cysteine proteases by peptidomimetic inhibitors.” 2017. Thesis, University of Adelaide. Accessed March 06, 2021. http://hdl.handle.net/2440/126464.

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

MLA Handbook (7th Edition):

Schumann, Nicholas. “Inhibition of serine and cysteine proteases by peptidomimetic inhibitors.” 2017. Web. 06 Mar 2021.

Vancouver:

Schumann N. Inhibition of serine and cysteine proteases by peptidomimetic inhibitors. [Internet] [Thesis]. University of Adelaide; 2017. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/2440/126464.

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

Council of Science Editors:

Schumann N. Inhibition of serine and cysteine proteases by peptidomimetic inhibitors. [Thesis]. University of Adelaide; 2017. Available from: http://hdl.handle.net/2440/126464

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

6. Manzur Ali, P P. Studies on physicochemical and biological properties of protease inhibitor from edible mushroom Pleurotus floridanus.

Degree: Biotechnology, 2012, Cochin University of Science and Technology

Protease inhibitors are found abundantly in numerous plants, animals and microorganisms, owing their significance to their application in the study of enzyme structures, reaction mechanisms… (more)

Subjects/Keywords: Proteases,; Protease inhibitors; Classification of protease inhibitors; Screening of mushrooms

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APA (6th Edition):

Manzur Ali, P. P. (2012). Studies on physicochemical and biological properties of protease inhibitor from edible mushroom Pleurotus floridanus. (Thesis). Cochin University of Science and Technology. Retrieved from http://dyuthi.cusat.ac.in/purl/3681

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):

Manzur Ali, P P. “Studies on physicochemical and biological properties of protease inhibitor from edible mushroom Pleurotus floridanus.” 2012. Thesis, Cochin University of Science and Technology. Accessed March 06, 2021. http://dyuthi.cusat.ac.in/purl/3681.

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

MLA Handbook (7th Edition):

Manzur Ali, P P. “Studies on physicochemical and biological properties of protease inhibitor from edible mushroom Pleurotus floridanus.” 2012. Web. 06 Mar 2021.

Vancouver:

Manzur Ali PP. Studies on physicochemical and biological properties of protease inhibitor from edible mushroom Pleurotus floridanus. [Internet] [Thesis]. Cochin University of Science and Technology; 2012. [cited 2021 Mar 06]. Available from: http://dyuthi.cusat.ac.in/purl/3681.

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

Council of Science Editors:

Manzur Ali PP. Studies on physicochemical and biological properties of protease inhibitor from edible mushroom Pleurotus floridanus. [Thesis]. Cochin University of Science and Technology; 2012. Available from: http://dyuthi.cusat.ac.in/purl/3681

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

7. Gupta, V K. Protease inhibitors in indian legumes: isolation and characterization of trypsin inhibitor from kidney beans; -.

Degree: Biochemistry, 2014, Kurukshetra University

None

Reference given

Advisors/Committee Members: Mittal, Anuradha.

Subjects/Keywords: inhibitors; isolation; Protease

Page 1 Page 2

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APA (6th Edition):

Gupta, V. K. (2014). Protease inhibitors in indian legumes: isolation and characterization of trypsin inhibitor from kidney beans; -. (Thesis). Kurukshetra University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/37530

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):

Gupta, V K. “Protease inhibitors in indian legumes: isolation and characterization of trypsin inhibitor from kidney beans; -.” 2014. Thesis, Kurukshetra University. Accessed March 06, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/37530.

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

MLA Handbook (7th Edition):

Gupta, V K. “Protease inhibitors in indian legumes: isolation and characterization of trypsin inhibitor from kidney beans; -.” 2014. Web. 06 Mar 2021.

Vancouver:

Gupta VK. Protease inhibitors in indian legumes: isolation and characterization of trypsin inhibitor from kidney beans; -. [Internet] [Thesis]. Kurukshetra University; 2014. [cited 2021 Mar 06]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/37530.

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

Council of Science Editors:

Gupta VK. Protease inhibitors in indian legumes: isolation and characterization of trypsin inhibitor from kidney beans; -. [Thesis]. Kurukshetra University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/37530

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


Boston University

8. Gillcrist, Marion. HIV, cardiovascular disease, anti-retroviral resistance: the issue with protease inhibitors and a need for alternatives.

Degree: MS, Medical Sciences, 2020, Boston University

 Today, it is estimated that 35 million people are living with human immunodeficiency virus (HIV). Since its initial discovery in 1981, researchers and medical providers… (more)

Subjects/Keywords: Medicine; Cardiovascular disease; HIV; Inflammation; Protease inhibitors

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APA (6th Edition):

Gillcrist, M. (2020). HIV, cardiovascular disease, anti-retroviral resistance: the issue with protease inhibitors and a need for alternatives. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/41243

Chicago Manual of Style (16th Edition):

Gillcrist, Marion. “HIV, cardiovascular disease, anti-retroviral resistance: the issue with protease inhibitors and a need for alternatives.” 2020. Masters Thesis, Boston University. Accessed March 06, 2021. http://hdl.handle.net/2144/41243.

MLA Handbook (7th Edition):

Gillcrist, Marion. “HIV, cardiovascular disease, anti-retroviral resistance: the issue with protease inhibitors and a need for alternatives.” 2020. Web. 06 Mar 2021.

Vancouver:

Gillcrist M. HIV, cardiovascular disease, anti-retroviral resistance: the issue with protease inhibitors and a need for alternatives. [Internet] [Masters thesis]. Boston University; 2020. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/2144/41243.

Council of Science Editors:

Gillcrist M. HIV, cardiovascular disease, anti-retroviral resistance: the issue with protease inhibitors and a need for alternatives. [Masters Thesis]. Boston University; 2020. Available from: http://hdl.handle.net/2144/41243


University of Illinois – Chicago

9. Siklos, Marton I. Covalent Enzyme Inhibitors in Drug Design.

Degree: 2016, University of Illinois – Chicago

 Epoxysuccinates have shown promising activity as irreversible inhibitors of calpain and cathepsin in indications from cancer to Alzheimer’s disease (AD). Their poor pharmacokinetic properties have… (more)

Subjects/Keywords: cysteine protease inhibitors; calpain; cathepsin B; epoxysuccinate

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APA (6th Edition):

Siklos, M. I. (2016). Covalent Enzyme Inhibitors in Drug Design. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/20226

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):

Siklos, Marton I. “Covalent Enzyme Inhibitors in Drug Design.” 2016. Thesis, University of Illinois – Chicago. Accessed March 06, 2021. http://hdl.handle.net/10027/20226.

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

MLA Handbook (7th Edition):

Siklos, Marton I. “Covalent Enzyme Inhibitors in Drug Design.” 2016. Web. 06 Mar 2021.

Vancouver:

Siklos MI. Covalent Enzyme Inhibitors in Drug Design. [Internet] [Thesis]. University of Illinois – Chicago; 2016. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/10027/20226.

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

Council of Science Editors:

Siklos MI. Covalent Enzyme Inhibitors in Drug Design. [Thesis]. University of Illinois – Chicago; 2016. Available from: http://hdl.handle.net/10027/20226

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


Kansas State University

10. Prior, Allan Mark. Synthesis and anti-viral activity of novel tripeptidyl compounds, modification of graphene oxides, and synthesis of peptidyl substrates for use in an electrochemical biosensor device.

Degree: PhD, Department of Chemistry, 2013, Kansas State University

 Three research projects are described in this dissertation and they consist of the discovery of norovirus protease inhibitors, modification of graphene oxides (GO) for the… (more)

Subjects/Keywords: Viral protease inhibitors; 3C protease and 3C-like protease inhibitors; Modification of graphene oxides; Chemistry (0485)

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APA (6th Edition):

Prior, A. M. (2013). Synthesis and anti-viral activity of novel tripeptidyl compounds, modification of graphene oxides, and synthesis of peptidyl substrates for use in an electrochemical biosensor device. (Doctoral Dissertation). Kansas State University. Retrieved from http://hdl.handle.net/2097/27654

Chicago Manual of Style (16th Edition):

Prior, Allan Mark. “Synthesis and anti-viral activity of novel tripeptidyl compounds, modification of graphene oxides, and synthesis of peptidyl substrates for use in an electrochemical biosensor device.” 2013. Doctoral Dissertation, Kansas State University. Accessed March 06, 2021. http://hdl.handle.net/2097/27654.

MLA Handbook (7th Edition):

Prior, Allan Mark. “Synthesis and anti-viral activity of novel tripeptidyl compounds, modification of graphene oxides, and synthesis of peptidyl substrates for use in an electrochemical biosensor device.” 2013. Web. 06 Mar 2021.

Vancouver:

Prior AM. Synthesis and anti-viral activity of novel tripeptidyl compounds, modification of graphene oxides, and synthesis of peptidyl substrates for use in an electrochemical biosensor device. [Internet] [Doctoral dissertation]. Kansas State University; 2013. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/2097/27654.

Council of Science Editors:

Prior AM. Synthesis and anti-viral activity of novel tripeptidyl compounds, modification of graphene oxides, and synthesis of peptidyl substrates for use in an electrochemical biosensor device. [Doctoral Dissertation]. Kansas State University; 2013. Available from: http://hdl.handle.net/2097/27654

11. Sapna, K. Isolation, purification, characterization and application of proteinaceous protease inhibitor from marine bacterium Pseudomonas mendocina BTMW 301.

Degree: Biotechnology, 2013, Cochin University of Science and Technology

The microorganisms are recognized as important sources of protease inhibitors which are valuable in the fields of medicine, agriculture and biotechnology. The protease inhibitors of… (more)

Subjects/Keywords: Proteases; Protease inhibitors; Competitive inhibition; Exosite binding; Therapeutic agents Proteinaceous inhibitors

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APA (6th Edition):

Sapna, K. (2013). Isolation, purification, characterization and application of proteinaceous protease inhibitor from marine bacterium Pseudomonas mendocina BTMW 301. (Thesis). Cochin University of Science and Technology. Retrieved from http://dyuthi.cusat.ac.in/purl/3717

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):

Sapna, K. “Isolation, purification, characterization and application of proteinaceous protease inhibitor from marine bacterium Pseudomonas mendocina BTMW 301.” 2013. Thesis, Cochin University of Science and Technology. Accessed March 06, 2021. http://dyuthi.cusat.ac.in/purl/3717.

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

MLA Handbook (7th Edition):

Sapna, K. “Isolation, purification, characterization and application of proteinaceous protease inhibitor from marine bacterium Pseudomonas mendocina BTMW 301.” 2013. Web. 06 Mar 2021.

Vancouver:

Sapna K. Isolation, purification, characterization and application of proteinaceous protease inhibitor from marine bacterium Pseudomonas mendocina BTMW 301. [Internet] [Thesis]. Cochin University of Science and Technology; 2013. [cited 2021 Mar 06]. Available from: http://dyuthi.cusat.ac.in/purl/3717.

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

Council of Science Editors:

Sapna K. Isolation, purification, characterization and application of proteinaceous protease inhibitor from marine bacterium Pseudomonas mendocina BTMW 301. [Thesis]. Cochin University of Science and Technology; 2013. Available from: http://dyuthi.cusat.ac.in/purl/3717

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


Latrobe University

12. 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 March 06, 2021. http://hdl.handle.net/1959.9/495861.

MLA Handbook (7th Edition):

Brand, Ingo Lothar. “Characterisation and identification of novel caspase inhibitors.” 2011. Web. 06 Mar 2021.

Vancouver:

Brand IL. Characterisation and identification of novel caspase inhibitors. [Internet] [Doctoral dissertation]. Latrobe University; 2011. [cited 2021 Mar 06]. 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


University of Johannesburg

13. 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


University of Pretoria

14. [No author]. Detection of protease and protease inhibitors during development of soybean crown nodules .

Degree: 2010, University of Pretoria

 A symbiotic association between leguminous roots and soil fixing nitrogen bacteria is required for legume nodule formation. The primary function of nodules is the fixation… (more)

Subjects/Keywords: Protease inhibitors; Legume nodule formation; Soybean crown nodules; UCTD

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APA (6th Edition):

author], [. (2010). Detection of protease and protease inhibitors during development of soybean crown nodules . (Masters Thesis). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-11232010-114246/

Chicago Manual of Style (16th Edition):

author], [No. “Detection of protease and protease inhibitors during development of soybean crown nodules .” 2010. Masters Thesis, University of Pretoria. Accessed March 06, 2021. http://upetd.up.ac.za/thesis/available/etd-11232010-114246/.

MLA Handbook (7th Edition):

author], [No. “Detection of protease and protease inhibitors during development of soybean crown nodules .” 2010. Web. 06 Mar 2021.

Vancouver:

author] [. Detection of protease and protease inhibitors during development of soybean crown nodules . [Internet] [Masters thesis]. University of Pretoria; 2010. [cited 2021 Mar 06]. Available from: http://upetd.up.ac.za/thesis/available/etd-11232010-114246/.

Council of Science Editors:

author] [. Detection of protease and protease inhibitors during development of soybean crown nodules . [Masters Thesis]. University of Pretoria; 2010. Available from: http://upetd.up.ac.za/thesis/available/etd-11232010-114246/

15. Akita, Nobuyuki. Host protein C inhibitor inhibits tumor growth, but promotes tumor metastasis, which is closely correlated with hypercoagulability.

Degree: 博士(医学), 2017, Mie University / 三重大学

Introduction: Protein C inhibitor (PCI), a member of the serine protease inhibitor family, is expressed in various human tissues, including liver and kidneys. In the… (more)

Subjects/Keywords: Protein C inhibitor; Serine protease inhibitors; Neoplasm metastasis; Protein C; Thrombomodulin

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APA (6th Edition):

Akita, N. (2017). Host protein C inhibitor inhibits tumor growth, but promotes tumor metastasis, which is closely correlated with hypercoagulability. (Thesis). Mie University / 三重大学. Retrieved from http://hdl.handle.net/10076/00017102

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):

Akita, Nobuyuki. “Host protein C inhibitor inhibits tumor growth, but promotes tumor metastasis, which is closely correlated with hypercoagulability.” 2017. Thesis, Mie University / 三重大学. Accessed March 06, 2021. http://hdl.handle.net/10076/00017102.

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

MLA Handbook (7th Edition):

Akita, Nobuyuki. “Host protein C inhibitor inhibits tumor growth, but promotes tumor metastasis, which is closely correlated with hypercoagulability.” 2017. Web. 06 Mar 2021.

Vancouver:

Akita N. Host protein C inhibitor inhibits tumor growth, but promotes tumor metastasis, which is closely correlated with hypercoagulability. [Internet] [Thesis]. Mie University / 三重大学; 2017. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/10076/00017102.

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

Council of Science Editors:

Akita N. Host protein C inhibitor inhibits tumor growth, but promotes tumor metastasis, which is closely correlated with hypercoagulability. [Thesis]. Mie University / 三重大学; 2017. Available from: http://hdl.handle.net/10076/00017102

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


Temple University

16. Kim, Jin Kyung. Syntheses of Silanediol Amino acids and alpha-amino-alpha-alkylsilanediol precursors.

Degree: PhD, 2008, Temple University

Chemistry

Two research projects are described: studies of the synthesis of alpha-amino-alpha-alkylsilanes, the synthetic precursor of silanediol-based protease inhibitors, and the synthesis and stability evaluation… (more)

Subjects/Keywords: Chemistry, Organic; silanediol; aziridine; aminosilane; protease inhibitors; organosilane

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

APA (6th Edition):

Kim, J. K. (2008). Syntheses of Silanediol Amino acids and alpha-amino-alpha-alkylsilanediol precursors. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,16809

Chicago Manual of Style (16th Edition):

Kim, Jin Kyung. “Syntheses of Silanediol Amino acids and alpha-amino-alpha-alkylsilanediol precursors.” 2008. Doctoral Dissertation, Temple University. Accessed March 06, 2021. http://digital.library.temple.edu/u?/p245801coll10,16809.

MLA Handbook (7th Edition):

Kim, Jin Kyung. “Syntheses of Silanediol Amino acids and alpha-amino-alpha-alkylsilanediol precursors.” 2008. Web. 06 Mar 2021.

Vancouver:

Kim JK. Syntheses of Silanediol Amino acids and alpha-amino-alpha-alkylsilanediol precursors. [Internet] [Doctoral dissertation]. Temple University; 2008. [cited 2021 Mar 06]. Available from: http://digital.library.temple.edu/u?/p245801coll10,16809.

Council of Science Editors:

Kim JK. Syntheses of Silanediol Amino acids and alpha-amino-alpha-alkylsilanediol precursors. [Doctoral Dissertation]. Temple University; 2008. Available from: http://digital.library.temple.edu/u?/p245801coll10,16809

17. HARPREET KAUR. Influence of Serine Plant Protease Inhibitors on the Growth Survival and Activity of Some Enzymes of Bactrocera cucurbitae CoqTephritidae Diptera; No.

Degree: Science, 2014, Guru Nanak Dev University

newline Available

Summary:111-117,Reference:118-148, Appendix:on the last pages

Advisors/Committee Members: Satwinder kaur.

Subjects/Keywords: Serine Plant Protease Inhibitors

Page 1

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APA (6th Edition):

KAUR, H. (2014). Influence of Serine Plant Protease Inhibitors on the Growth Survival and Activity of Some Enzymes of Bactrocera cucurbitae CoqTephritidae Diptera; No. (Thesis). Guru Nanak Dev University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/29763

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):

KAUR, HARPREET. “Influence of Serine Plant Protease Inhibitors on the Growth Survival and Activity of Some Enzymes of Bactrocera cucurbitae CoqTephritidae Diptera; No.” 2014. Thesis, Guru Nanak Dev University. Accessed March 06, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/29763.

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

MLA Handbook (7th Edition):

KAUR, HARPREET. “Influence of Serine Plant Protease Inhibitors on the Growth Survival and Activity of Some Enzymes of Bactrocera cucurbitae CoqTephritidae Diptera; No.” 2014. Web. 06 Mar 2021.

Vancouver:

KAUR H. Influence of Serine Plant Protease Inhibitors on the Growth Survival and Activity of Some Enzymes of Bactrocera cucurbitae CoqTephritidae Diptera; No. [Internet] [Thesis]. Guru Nanak Dev University; 2014. [cited 2021 Mar 06]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/29763.

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

Council of Science Editors:

KAUR H. Influence of Serine Plant Protease Inhibitors on the Growth Survival and Activity of Some Enzymes of Bactrocera cucurbitae CoqTephritidae Diptera; No. [Thesis]. Guru Nanak Dev University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/29763

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

18. Pribut, Nicole. Design and Synthesis of potent benzimidazolone HIV Non-nucleoside reverse transcriptase inhibitors.

Degree: PhD, Chemistry and Polymer Science, 2018, Stellenbosch University

 ENGLISH ABSTRACT: Since the 1980’s, HIV has plagued the population on a global scale, with millions of newly infected individuals reported every year. However, with… (more)

Subjects/Keywords: HIV; NNRTIs; AIDS-associated retrovirus; Protease inhibitors; Antiretroviral drugs

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APA (6th Edition):

Pribut, N. (2018). Design and Synthesis of potent benzimidazolone HIV Non-nucleoside reverse transcriptase inhibitors. (Doctoral Dissertation). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/105138

Chicago Manual of Style (16th Edition):

Pribut, Nicole. “Design and Synthesis of potent benzimidazolone HIV Non-nucleoside reverse transcriptase inhibitors.” 2018. Doctoral Dissertation, Stellenbosch University. Accessed March 06, 2021. http://hdl.handle.net/10019.1/105138.

MLA Handbook (7th Edition):

Pribut, Nicole. “Design and Synthesis of potent benzimidazolone HIV Non-nucleoside reverse transcriptase inhibitors.” 2018. Web. 06 Mar 2021.

Vancouver:

Pribut N. Design and Synthesis of potent benzimidazolone HIV Non-nucleoside reverse transcriptase inhibitors. [Internet] [Doctoral dissertation]. Stellenbosch University; 2018. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/10019.1/105138.

Council of Science Editors:

Pribut N. Design and Synthesis of potent benzimidazolone HIV Non-nucleoside reverse transcriptase inhibitors. [Doctoral Dissertation]. Stellenbosch University; 2018. Available from: http://hdl.handle.net/10019.1/105138


University of Texas Southwestern Medical Center

19. Sul, Soon-Hee. Insights into the Serpin Inhibitory Mechanism from Structures of Mutant Serpins in the Mechaelis Complex.

Degree: 2008, University of Texas Southwestern Medical Center

 The serpins belong to a superfamily of protease inhibitors that employ a unique suicide substrate-like inhibitory mechanism. In this mechanism, target protease becomes acylated at… (more)

Subjects/Keywords: Protease Inhibitors; Serpins; Hydrolysis

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APA (6th Edition):

Sul, S. (2008). Insights into the Serpin Inhibitory Mechanism from Structures of Mutant Serpins in the Mechaelis Complex. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/457

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):

Sul, Soon-Hee. “Insights into the Serpin Inhibitory Mechanism from Structures of Mutant Serpins in the Mechaelis Complex.” 2008. Thesis, University of Texas Southwestern Medical Center. Accessed March 06, 2021. http://hdl.handle.net/2152.5/457.

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

MLA Handbook (7th Edition):

Sul, Soon-Hee. “Insights into the Serpin Inhibitory Mechanism from Structures of Mutant Serpins in the Mechaelis Complex.” 2008. Web. 06 Mar 2021.

Vancouver:

Sul S. Insights into the Serpin Inhibitory Mechanism from Structures of Mutant Serpins in the Mechaelis Complex. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2008. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/2152.5/457.

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

Council of Science Editors:

Sul S. Insights into the Serpin Inhibitory Mechanism from Structures of Mutant Serpins in the Mechaelis Complex. [Thesis]. University of Texas Southwestern Medical Center; 2008. Available from: http://hdl.handle.net/2152.5/457

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

20. Sutheera Khantaphant. Proteases from pyloric caeca of brownstripe red snapper (Lutjanus vitta): Purification, characterization and the use for production of hydrolysate with antioxidative activity .

Degree: 2010, Prince of Songkla University

Subjects/Keywords: Proteolytic enzymes; Protease inhibitors

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APA (6th Edition):

Khantaphant, S. (2010). Proteases from pyloric caeca of brownstripe red snapper (Lutjanus vitta): Purification, characterization and the use for production of hydrolysate with antioxidative activity . (Thesis). Prince of Songkla University. Retrieved from http://kb.psu.ac.th/psukb/handle/2010/7171

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):

Khantaphant, Sutheera. “Proteases from pyloric caeca of brownstripe red snapper (Lutjanus vitta): Purification, characterization and the use for production of hydrolysate with antioxidative activity .” 2010. Thesis, Prince of Songkla University. Accessed March 06, 2021. http://kb.psu.ac.th/psukb/handle/2010/7171.

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

MLA Handbook (7th Edition):

Khantaphant, Sutheera. “Proteases from pyloric caeca of brownstripe red snapper (Lutjanus vitta): Purification, characterization and the use for production of hydrolysate with antioxidative activity .” 2010. Web. 06 Mar 2021.

Vancouver:

Khantaphant S. Proteases from pyloric caeca of brownstripe red snapper (Lutjanus vitta): Purification, characterization and the use for production of hydrolysate with antioxidative activity . [Internet] [Thesis]. Prince of Songkla University; 2010. [cited 2021 Mar 06]. Available from: http://kb.psu.ac.th/psukb/handle/2010/7171.

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

Council of Science Editors:

Khantaphant S. Proteases from pyloric caeca of brownstripe red snapper (Lutjanus vitta): Purification, characterization and the use for production of hydrolysate with antioxidative activity . [Thesis]. Prince of Songkla University; 2010. Available from: http://kb.psu.ac.th/psukb/handle/2010/7171

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


University of Pretoria

21. Mashamba, Lufuno Abigail. Detection of protease and protease inhibitors during development of soybean crown nodules.

Degree: Plant Science, 2010, University of Pretoria

 A symbiotic association between leguminous roots and soil fixing nitrogen bacteria is required for legume nodule formation. The primary function of nodules is the fixation… (more)

Subjects/Keywords: Protease inhibitors; Legume nodule formation; Soybean crown nodules; UCTD

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APA (6th Edition):

Mashamba, L. (2010). Detection of protease and protease inhibitors during development of soybean crown nodules. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/29724

Chicago Manual of Style (16th Edition):

Mashamba, Lufuno. “Detection of protease and protease inhibitors during development of soybean crown nodules.” 2010. Masters Thesis, University of Pretoria. Accessed March 06, 2021. http://hdl.handle.net/2263/29724.

MLA Handbook (7th Edition):

Mashamba, Lufuno. “Detection of protease and protease inhibitors during development of soybean crown nodules.” 2010. Web. 06 Mar 2021.

Vancouver:

Mashamba L. Detection of protease and protease inhibitors during development of soybean crown nodules. [Internet] [Masters thesis]. University of Pretoria; 2010. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/2263/29724.

Council of Science Editors:

Mashamba L. Detection of protease and protease inhibitors during development of soybean crown nodules. [Masters Thesis]. University of Pretoria; 2010. Available from: http://hdl.handle.net/2263/29724


Brigham Young University

22. Gross, Andrew Jacob. Discovery of an Allosteric Site on Furin, contributing to Potent Inhibition: A Promising Therapeutic for the Anemia of Chronic Inflammation.

Degree: PhD, 2014, Brigham Young University

 Anemia of chronic inflammation (ACI) is a condition that develops in a setting of chronic immune activation. ACI is characterized and triggered by inflammatory cytokines… (more)

Subjects/Keywords: furin; anemia of chronic inflammation; hepcidin; protease inhibitors; ferroportin; Chemistry

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APA (6th Edition):

Gross, A. J. (2014). Discovery of an Allosteric Site on Furin, contributing to Potent Inhibition: A Promising Therapeutic for the Anemia of Chronic Inflammation. (Doctoral Dissertation). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7537&context=etd

Chicago Manual of Style (16th Edition):

Gross, Andrew Jacob. “Discovery of an Allosteric Site on Furin, contributing to Potent Inhibition: A Promising Therapeutic for the Anemia of Chronic Inflammation.” 2014. Doctoral Dissertation, Brigham Young University. Accessed March 06, 2021. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7537&context=etd.

MLA Handbook (7th Edition):

Gross, Andrew Jacob. “Discovery of an Allosteric Site on Furin, contributing to Potent Inhibition: A Promising Therapeutic for the Anemia of Chronic Inflammation.” 2014. Web. 06 Mar 2021.

Vancouver:

Gross AJ. Discovery of an Allosteric Site on Furin, contributing to Potent Inhibition: A Promising Therapeutic for the Anemia of Chronic Inflammation. [Internet] [Doctoral dissertation]. Brigham Young University; 2014. [cited 2021 Mar 06]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7537&context=etd.

Council of Science Editors:

Gross AJ. Discovery of an Allosteric Site on Furin, contributing to Potent Inhibition: A Promising Therapeutic for the Anemia of Chronic Inflammation. [Doctoral Dissertation]. Brigham Young University; 2014. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7537&context=etd


Rhodes University

23. Sigauke, Lester Takunda. An in-silico investigation of Morita-Baylis-Hillman accessible heterocyclic analogues for applications as novel HIV-1 C protease inhibitors.

Degree: Faculty of Science, Biochemistry and Microbiology, 2015, Rhodes University

 Cheminformatic approaches have been employed to optimize the bis-coumarin scaffold identified by Onywera et al. (2012) as a potential hit against the protease HIV-1 protein.… (more)

Subjects/Keywords: Protease inhibitors; Heterocyclic compounds; HIV (Viruses); HIV infections; Drug resistance; Cheminformatics

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APA (6th Edition):

Sigauke, L. T. (2015). An in-silico investigation of Morita-Baylis-Hillman accessible heterocyclic analogues for applications as novel HIV-1 C protease inhibitors. (Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1017913

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):

Sigauke, Lester Takunda. “An in-silico investigation of Morita-Baylis-Hillman accessible heterocyclic analogues for applications as novel HIV-1 C protease inhibitors.” 2015. Thesis, Rhodes University. Accessed March 06, 2021. http://hdl.handle.net/10962/d1017913.

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

MLA Handbook (7th Edition):

Sigauke, Lester Takunda. “An in-silico investigation of Morita-Baylis-Hillman accessible heterocyclic analogues for applications as novel HIV-1 C protease inhibitors.” 2015. Web. 06 Mar 2021.

Vancouver:

Sigauke LT. An in-silico investigation of Morita-Baylis-Hillman accessible heterocyclic analogues for applications as novel HIV-1 C protease inhibitors. [Internet] [Thesis]. Rhodes University; 2015. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/10962/d1017913.

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

Council of Science Editors:

Sigauke LT. An in-silico investigation of Morita-Baylis-Hillman accessible heterocyclic analogues for applications as novel HIV-1 C protease inhibitors. [Thesis]. Rhodes University; 2015. Available from: http://hdl.handle.net/10962/d1017913

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


University of Toronto

24. Tan, Joanne. New Methodologies for the Synthesis of Aminoboronic Acids and Tetrahydroquinolines.

Degree: PhD, 2020, University of Toronto

 There has been a rising interest in aminoboronic acids since their medicinal properties have been realized. Thus, new strategies for the synthesis of α- and… (more)

Subjects/Keywords: boron; caseinolytic protease P; inhibitors; multicomponent reactions; photochemistry; serine hydrolases; 0490

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APA (6th Edition):

Tan, J. (2020). New Methodologies for the Synthesis of Aminoboronic Acids and Tetrahydroquinolines. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/100953

Chicago Manual of Style (16th Edition):

Tan, Joanne. “New Methodologies for the Synthesis of Aminoboronic Acids and Tetrahydroquinolines.” 2020. Doctoral Dissertation, University of Toronto. Accessed March 06, 2021. http://hdl.handle.net/1807/100953.

MLA Handbook (7th Edition):

Tan, Joanne. “New Methodologies for the Synthesis of Aminoboronic Acids and Tetrahydroquinolines.” 2020. Web. 06 Mar 2021.

Vancouver:

Tan J. New Methodologies for the Synthesis of Aminoboronic Acids and Tetrahydroquinolines. [Internet] [Doctoral dissertation]. University of Toronto; 2020. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1807/100953.

Council of Science Editors:

Tan J. New Methodologies for the Synthesis of Aminoboronic Acids and Tetrahydroquinolines. [Doctoral Dissertation]. University of Toronto; 2020. Available from: http://hdl.handle.net/1807/100953


Hong Kong University of Science and Technology

25. Mak, Pui Ying. Efficacy of targeting the ATR-CHK1-WEE1 pathway in the G2 DNA damage checkpoint as potential anti-cancer therapy.

Degree: 2014, Hong Kong University of Science and Technology

 Nasopharyngeal carcinoma (NPC) is a rare but highly invasive cancer. Radiotherapy is the primary approach for NPC treatment. However, activating the ATR-CHK1-WEE1 axis with ionizing… (more)

Subjects/Keywords: Nasopharynx ; Cancer ; Treatment ; Protease inhibitors ; Protein kinases ; DNA damage

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APA (6th Edition):

Mak, P. Y. (2014). Efficacy of targeting the ATR-CHK1-WEE1 pathway in the G2 DNA damage checkpoint as potential anti-cancer therapy. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-73432 ; https://doi.org/10.14711/thesis-b1334210 ; http://repository.ust.hk/ir/bitstream/1783.1-73432/1/th_redirect.html

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):

Mak, Pui Ying. “Efficacy of targeting the ATR-CHK1-WEE1 pathway in the G2 DNA damage checkpoint as potential anti-cancer therapy.” 2014. Thesis, Hong Kong University of Science and Technology. Accessed March 06, 2021. http://repository.ust.hk/ir/Record/1783.1-73432 ; https://doi.org/10.14711/thesis-b1334210 ; http://repository.ust.hk/ir/bitstream/1783.1-73432/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Mak, Pui Ying. “Efficacy of targeting the ATR-CHK1-WEE1 pathway in the G2 DNA damage checkpoint as potential anti-cancer therapy.” 2014. Web. 06 Mar 2021.

Vancouver:

Mak PY. Efficacy of targeting the ATR-CHK1-WEE1 pathway in the G2 DNA damage checkpoint as potential anti-cancer therapy. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2021 Mar 06]. Available from: http://repository.ust.hk/ir/Record/1783.1-73432 ; https://doi.org/10.14711/thesis-b1334210 ; http://repository.ust.hk/ir/bitstream/1783.1-73432/1/th_redirect.html.

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

Council of Science Editors:

Mak PY. Efficacy of targeting the ATR-CHK1-WEE1 pathway in the G2 DNA damage checkpoint as potential anti-cancer therapy. [Thesis]. Hong Kong University of Science and Technology; 2014. Available from: http://repository.ust.hk/ir/Record/1783.1-73432 ; https://doi.org/10.14711/thesis-b1334210 ; http://repository.ust.hk/ir/bitstream/1783.1-73432/1/th_redirect.html

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


Rice University

26. Strom, T. Amanda. C60 Amino Acids and Peptides.

Degree: PhD, Natural Sciences, 2011, Rice University

 Since the discovery of the buckyball in 1985, researchers have imagined its potential in fields ranging from materials science to medicinal chemistry. The unique size,… (more)

Subjects/Keywords: Pure sciences; Fullerenes; Amino acids; Protease inhibitors; Graphene; Organic chemistry

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APA (6th Edition):

Strom, T. A. (2011). C60 Amino Acids and Peptides. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/70455

Chicago Manual of Style (16th Edition):

Strom, T Amanda. “C60 Amino Acids and Peptides.” 2011. Doctoral Dissertation, Rice University. Accessed March 06, 2021. http://hdl.handle.net/1911/70455.

MLA Handbook (7th Edition):

Strom, T Amanda. “C60 Amino Acids and Peptides.” 2011. Web. 06 Mar 2021.

Vancouver:

Strom TA. C60 Amino Acids and Peptides. [Internet] [Doctoral dissertation]. Rice University; 2011. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1911/70455.

Council of Science Editors:

Strom TA. C60 Amino Acids and Peptides. [Doctoral Dissertation]. Rice University; 2011. Available from: http://hdl.handle.net/1911/70455


University of Cape Town

27. Fletcher, Jean Margaret. Proteolytic mechanisms involved in the metastasis of human melanoma cells.

Degree: Image, Division of Chemical Pathology, 1994, University of Cape Town

 The metastatic process requires that tumour cells are capable of traversing various micro-environmental barriers, such as the basement membrane. There are various proteolytic mechanisms which… (more)

Subjects/Keywords: Melanoma; Neoplasm metastasis; Protease inhibitors

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APA (6th Edition):

Fletcher, J. M. (1994). Proteolytic mechanisms involved in the metastasis of human melanoma cells. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/27116

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):

Fletcher, Jean Margaret. “Proteolytic mechanisms involved in the metastasis of human melanoma cells.” 1994. Thesis, University of Cape Town. Accessed March 06, 2021. http://hdl.handle.net/11427/27116.

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

MLA Handbook (7th Edition):

Fletcher, Jean Margaret. “Proteolytic mechanisms involved in the metastasis of human melanoma cells.” 1994. Web. 06 Mar 2021.

Vancouver:

Fletcher JM. Proteolytic mechanisms involved in the metastasis of human melanoma cells. [Internet] [Thesis]. University of Cape Town; 1994. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/11427/27116.

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

Council of Science Editors:

Fletcher JM. Proteolytic mechanisms involved in the metastasis of human melanoma cells. [Thesis]. University of Cape Town; 1994. Available from: http://hdl.handle.net/11427/27116

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


Brock University

28. Tays, Kevin. Aryl hydroxamic acid analogues as potential therapeutic agents .

Degree: Department of Chemistry, 1997, Brock University

 A new synthetic pathway to analogues of the aglucones of naturally occurring cyclic hydroxamic acids (2,4-dihydroxy-l,4-benzoxazin-3-ones) has been developed. The new pathway involves the coupling… (more)

Subjects/Keywords: Hydroxamic acids.; Protease inhibitors.

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

APA (6th Edition):

Tays, K. (1997). Aryl hydroxamic acid analogues as potential therapeutic agents . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/1221

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):

Tays, Kevin. “Aryl hydroxamic acid analogues as potential therapeutic agents .” 1997. Thesis, Brock University. Accessed March 06, 2021. http://hdl.handle.net/10464/1221.

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

MLA Handbook (7th Edition):

Tays, Kevin. “Aryl hydroxamic acid analogues as potential therapeutic agents .” 1997. Web. 06 Mar 2021.

Vancouver:

Tays K. Aryl hydroxamic acid analogues as potential therapeutic agents . [Internet] [Thesis]. Brock University; 1997. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/10464/1221.

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

Council of Science Editors:

Tays K. Aryl hydroxamic acid analogues as potential therapeutic agents . [Thesis]. Brock University; 1997. Available from: http://hdl.handle.net/10464/1221

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


Georgia Tech

29. Ding, Yan Shirley. Expression, purification and charaterization of recombinant human T-cell leukemia virus type I protease.

Degree: PhD, Chemistry, 1998, Georgia Tech

Subjects/Keywords: HTLV-I (Virus); Protease inhibitors

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

APA (6th Edition):

Ding, Y. S. (1998). Expression, purification and charaterization of recombinant human T-cell leukemia virus type I protease. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/29992

Chicago Manual of Style (16th Edition):

Ding, Yan Shirley. “Expression, purification and charaterization of recombinant human T-cell leukemia virus type I protease.” 1998. Doctoral Dissertation, Georgia Tech. Accessed March 06, 2021. http://hdl.handle.net/1853/29992.

MLA Handbook (7th Edition):

Ding, Yan Shirley. “Expression, purification and charaterization of recombinant human T-cell leukemia virus type I protease.” 1998. Web. 06 Mar 2021.

Vancouver:

Ding YS. Expression, purification and charaterization of recombinant human T-cell leukemia virus type I protease. [Internet] [Doctoral dissertation]. Georgia Tech; 1998. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1853/29992.

Council of Science Editors:

Ding YS. Expression, purification and charaterization of recombinant human T-cell leukemia virus type I protease. [Doctoral Dissertation]. Georgia Tech; 1998. Available from: http://hdl.handle.net/1853/29992


Georgia Tech

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

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

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