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You searched for subject:(Proteasome). Showing records 1 – 30 of 429 total matches.

[1] [2] [3] [4] [5] … [15]

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University of Adelaide

1. Alaknanda, Alaknanda. Targeted therapies for the treatment of solid cancers.

Degree: 2017, University of Adelaide

 Cancer is the leading cause of the burden of disease and injury in Australia, accounting for approximately 19 percent of the total disease burden. In… (more)

Subjects/Keywords: Proteasome

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APA (6th Edition):

Alaknanda, A. (2017). Targeted therapies for the treatment of solid cancers. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/119676

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):

Alaknanda, Alaknanda. “Targeted therapies for the treatment of solid cancers.” 2017. Thesis, University of Adelaide. Accessed February 20, 2020. http://hdl.handle.net/2440/119676.

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

MLA Handbook (7th Edition):

Alaknanda, Alaknanda. “Targeted therapies for the treatment of solid cancers.” 2017. Web. 20 Feb 2020.

Vancouver:

Alaknanda A. Targeted therapies for the treatment of solid cancers. [Internet] [Thesis]. University of Adelaide; 2017. [cited 2020 Feb 20]. Available from: http://hdl.handle.net/2440/119676.

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

Council of Science Editors:

Alaknanda A. Targeted therapies for the treatment of solid cancers. [Thesis]. University of Adelaide; 2017. Available from: http://hdl.handle.net/2440/119676

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


Kansas State University

2. Waite, Kenrick. Molecular regulation of proteasome abundance and localization.

Degree: PhD, Department of Biology, 2019, Kansas State University

 Proteasomes are molecular complexes that degrade more than 80% of proteins in eukaryotes. This makes these proteases essential for processes associated with cell survival and… (more)

Subjects/Keywords: Proteasome; Autophagy; Proteasome storage granules

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APA (6th Edition):

Waite, K. (2019). Molecular regulation of proteasome abundance and localization. (Doctoral Dissertation). Kansas State University. Retrieved from http://hdl.handle.net/2097/40060

Chicago Manual of Style (16th Edition):

Waite, Kenrick. “Molecular regulation of proteasome abundance and localization.” 2019. Doctoral Dissertation, Kansas State University. Accessed February 20, 2020. http://hdl.handle.net/2097/40060.

MLA Handbook (7th Edition):

Waite, Kenrick. “Molecular regulation of proteasome abundance and localization.” 2019. Web. 20 Feb 2020.

Vancouver:

Waite K. Molecular regulation of proteasome abundance and localization. [Internet] [Doctoral dissertation]. Kansas State University; 2019. [cited 2020 Feb 20]. Available from: http://hdl.handle.net/2097/40060.

Council of Science Editors:

Waite K. Molecular regulation of proteasome abundance and localization. [Doctoral Dissertation]. Kansas State University; 2019. Available from: http://hdl.handle.net/2097/40060


University of Toronto

3. Cheng, Shuk Yee. Effects of Proteasome Inhibition on Tau Protein.

Degree: 2011, University of Toronto

The ubiquitin-proteasome system is an important proteolytic pathway implicated in the formation of neurofibrillary tangles from hyperphosphorylated tau, a pathological hallmark of tauopathies such as… (more)

Subjects/Keywords: Tau; Proteasome

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APA (6th Edition):

Cheng, S. Y. (2011). Effects of Proteasome Inhibition on Tau Protein. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/30547

Chicago Manual of Style (16th Edition):

Cheng, Shuk Yee. “Effects of Proteasome Inhibition on Tau Protein.” 2011. Masters Thesis, University of Toronto. Accessed February 20, 2020. http://hdl.handle.net/1807/30547.

MLA Handbook (7th Edition):

Cheng, Shuk Yee. “Effects of Proteasome Inhibition on Tau Protein.” 2011. Web. 20 Feb 2020.

Vancouver:

Cheng SY. Effects of Proteasome Inhibition on Tau Protein. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2020 Feb 20]. Available from: http://hdl.handle.net/1807/30547.

Council of Science Editors:

Cheng SY. Effects of Proteasome Inhibition on Tau Protein. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/30547


University of California – San Diego

4. Gonzales, Frankie Robert. Characterizing Postranslational Regulatory Mechanisms of the Ubiquitin Proteasome System.

Degree: Chemistry, 2017, University of California – San Diego

 Protein homeostasis in is critical to maintain cell health and viability. Protein homeostasis can be divided into two major categories: protein synthesis, and protein degradation.… (more)

Subjects/Keywords: Biochemistry; Proteasome; Ubiquitin

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APA (6th Edition):

Gonzales, F. R. (2017). Characterizing Postranslational Regulatory Mechanisms of the Ubiquitin Proteasome System. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/6958j596

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):

Gonzales, Frankie Robert. “Characterizing Postranslational Regulatory Mechanisms of the Ubiquitin Proteasome System.” 2017. Thesis, University of California – San Diego. Accessed February 20, 2020. http://www.escholarship.org/uc/item/6958j596.

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

MLA Handbook (7th Edition):

Gonzales, Frankie Robert. “Characterizing Postranslational Regulatory Mechanisms of the Ubiquitin Proteasome System.” 2017. Web. 20 Feb 2020.

Vancouver:

Gonzales FR. Characterizing Postranslational Regulatory Mechanisms of the Ubiquitin Proteasome System. [Internet] [Thesis]. University of California – San Diego; 2017. [cited 2020 Feb 20]. Available from: http://www.escholarship.org/uc/item/6958j596.

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

Council of Science Editors:

Gonzales FR. Characterizing Postranslational Regulatory Mechanisms of the Ubiquitin Proteasome System. [Thesis]. University of California – San Diego; 2017. Available from: http://www.escholarship.org/uc/item/6958j596

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


University of Alberta

5. Mottet, Kelly. The poxvirus ubiquitin ligase p28 manipulates the ubiquitin proteasome system.

Degree: MS, Department of Medical Microbiology and Immunology, 2010, University of Alberta

 The significance of poxvirus manipulation of the host ubiquitin proteasome system has become increasingly apparent. Ubiquitin is post-translationally added to target proteins by a highly… (more)

Subjects/Keywords: ligase; ubiquitination; proteasome; ubiquitin; poxvirus

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APA (6th Edition):

Mottet, K. (2010). The poxvirus ubiquitin ligase p28 manipulates the ubiquitin proteasome system. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/zp38wf105

Chicago Manual of Style (16th Edition):

Mottet, Kelly. “The poxvirus ubiquitin ligase p28 manipulates the ubiquitin proteasome system.” 2010. Masters Thesis, University of Alberta. Accessed February 20, 2020. https://era.library.ualberta.ca/files/zp38wf105.

MLA Handbook (7th Edition):

Mottet, Kelly. “The poxvirus ubiquitin ligase p28 manipulates the ubiquitin proteasome system.” 2010. Web. 20 Feb 2020.

Vancouver:

Mottet K. The poxvirus ubiquitin ligase p28 manipulates the ubiquitin proteasome system. [Internet] [Masters thesis]. University of Alberta; 2010. [cited 2020 Feb 20]. Available from: https://era.library.ualberta.ca/files/zp38wf105.

Council of Science Editors:

Mottet K. The poxvirus ubiquitin ligase p28 manipulates the ubiquitin proteasome system. [Masters Thesis]. University of Alberta; 2010. Available from: https://era.library.ualberta.ca/files/zp38wf105


University of Minnesota

6. Randles, Leah Ann. Defining how the 26S proteasome recognizes ubiquitinated substrates.

Degree: PhD, Biochemistry, Molecular Bio, and Biophysics, 2012, University of Minnesota

 Regulated protein degradation in eukaryotes is performed predominantly by the ubiquitin-proteasome pathway. Prior to their degradation by the 26S proteasome, protein substrates become covalently modified… (more)

Subjects/Keywords: Proteasome; Ubiquitin; Ubiquitin Receptor

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APA (6th Edition):

Randles, L. A. (2012). Defining how the 26S proteasome recognizes ubiquitinated substrates. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/162241

Chicago Manual of Style (16th Edition):

Randles, Leah Ann. “Defining how the 26S proteasome recognizes ubiquitinated substrates.” 2012. Doctoral Dissertation, University of Minnesota. Accessed February 20, 2020. http://hdl.handle.net/11299/162241.

MLA Handbook (7th Edition):

Randles, Leah Ann. “Defining how the 26S proteasome recognizes ubiquitinated substrates.” 2012. Web. 20 Feb 2020.

Vancouver:

Randles LA. Defining how the 26S proteasome recognizes ubiquitinated substrates. [Internet] [Doctoral dissertation]. University of Minnesota; 2012. [cited 2020 Feb 20]. Available from: http://hdl.handle.net/11299/162241.

Council of Science Editors:

Randles LA. Defining how the 26S proteasome recognizes ubiquitinated substrates. [Doctoral Dissertation]. University of Minnesota; 2012. Available from: http://hdl.handle.net/11299/162241

7. Nakamura, Kasumi. Effects of hydroxy groups in the A-ring on the anti-proteasome activity of flavone : フラボンの抗プロテアソーム活性におけるA環のヒドロキシル基の効果.

Degree: 博士(医学), 2016, Hamamatsu University School of Medicine / 浜松医科大学

The ubiquitin–proteasome pathway plays an important role in regulating apoptosis and the cell cycle. Recently, proteasome inhibitors have been shown to have antitumor effects and… (more)

Subjects/Keywords: ubiquitin; flavonoid; proteasome; inhibitor

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APA (6th Edition):

Nakamura, K. (2016). Effects of hydroxy groups in the A-ring on the anti-proteasome activity of flavone : フラボンの抗プロテアソーム活性におけるA環のヒドロキシル基の効果. (Thesis). Hamamatsu University School of Medicine / 浜松医科大学. Retrieved from http://hdl.handle.net/10271/3143

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):

Nakamura, Kasumi. “Effects of hydroxy groups in the A-ring on the anti-proteasome activity of flavone : フラボンの抗プロテアソーム活性におけるA環のヒドロキシル基の効果.” 2016. Thesis, Hamamatsu University School of Medicine / 浜松医科大学. Accessed February 20, 2020. http://hdl.handle.net/10271/3143.

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

MLA Handbook (7th Edition):

Nakamura, Kasumi. “Effects of hydroxy groups in the A-ring on the anti-proteasome activity of flavone : フラボンの抗プロテアソーム活性におけるA環のヒドロキシル基の効果.” 2016. Web. 20 Feb 2020.

Vancouver:

Nakamura K. Effects of hydroxy groups in the A-ring on the anti-proteasome activity of flavone : フラボンの抗プロテアソーム活性におけるA環のヒドロキシル基の効果. [Internet] [Thesis]. Hamamatsu University School of Medicine / 浜松医科大学; 2016. [cited 2020 Feb 20]. Available from: http://hdl.handle.net/10271/3143.

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

Council of Science Editors:

Nakamura K. Effects of hydroxy groups in the A-ring on the anti-proteasome activity of flavone : フラボンの抗プロテアソーム活性におけるA環のヒドロキシル基の効果. [Thesis]. Hamamatsu University School of Medicine / 浜松医科大学; 2016. Available from: http://hdl.handle.net/10271/3143

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


University of California – Berkeley

8. Worden, Evan Josiah. Structural and Functional Characterization of the Proteasomal Deubiquitinase Rpn11.

Degree: Molecular & Cell Biology, 2016, University of California – Berkeley

 The 26S proteasome is responsible for selective protein degradation in eukaryotic cells. Polyubiquitin chains mark proteins for degradation by the proteasome, but before degradation can… (more)

Subjects/Keywords: Biochemistry; deubiquitinase; proteasome; ubiquitin

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APA (6th Edition):

Worden, E. J. (2016). Structural and Functional Characterization of the Proteasomal Deubiquitinase Rpn11. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/2138s3gn

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):

Worden, Evan Josiah. “Structural and Functional Characterization of the Proteasomal Deubiquitinase Rpn11.” 2016. Thesis, University of California – Berkeley. Accessed February 20, 2020. http://www.escholarship.org/uc/item/2138s3gn.

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

MLA Handbook (7th Edition):

Worden, Evan Josiah. “Structural and Functional Characterization of the Proteasomal Deubiquitinase Rpn11.” 2016. Web. 20 Feb 2020.

Vancouver:

Worden EJ. Structural and Functional Characterization of the Proteasomal Deubiquitinase Rpn11. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2020 Feb 20]. Available from: http://www.escholarship.org/uc/item/2138s3gn.

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

Council of Science Editors:

Worden EJ. Structural and Functional Characterization of the Proteasomal Deubiquitinase Rpn11. [Thesis]. University of California – Berkeley; 2016. Available from: http://www.escholarship.org/uc/item/2138s3gn

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


University of Ottawa

9. Pundir, Sheetal. The Characterization of the Novel Chloroquine Derivative VR23 for its Anticancer Properties .

Degree: 2015, University of Ottawa

 Since Bortezomib®, a proteasome inhibitor, was approved by US FDA for the treatment of multiple myeloma in 2003, proteasome is recognized as one of the… (more)

Subjects/Keywords: Proteasome; Centrosome; Chloroquine; Anticancer

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APA (6th Edition):

Pundir, S. (2015). The Characterization of the Novel Chloroquine Derivative VR23 for its Anticancer Properties . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/32405

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):

Pundir, Sheetal. “The Characterization of the Novel Chloroquine Derivative VR23 for its Anticancer Properties .” 2015. Thesis, University of Ottawa. Accessed February 20, 2020. http://hdl.handle.net/10393/32405.

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

MLA Handbook (7th Edition):

Pundir, Sheetal. “The Characterization of the Novel Chloroquine Derivative VR23 for its Anticancer Properties .” 2015. Web. 20 Feb 2020.

Vancouver:

Pundir S. The Characterization of the Novel Chloroquine Derivative VR23 for its Anticancer Properties . [Internet] [Thesis]. University of Ottawa; 2015. [cited 2020 Feb 20]. Available from: http://hdl.handle.net/10393/32405.

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

Council of Science Editors:

Pundir S. The Characterization of the Novel Chloroquine Derivative VR23 for its Anticancer Properties . [Thesis]. University of Ottawa; 2015. Available from: http://hdl.handle.net/10393/32405

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


University of South Florida

10. Daily, Jennifer L. Efficacy of Increased Ube3a Protein Levels in the Brain in Rescuing the Phenotype of an Angelman Syndrome Mouse.

Degree: 2012, University of South Florida

 Angelman syndrome (AS), a genetic disorder occurring in approximately one in every 15,000 births, is characterized by severe mental retardation, seizures, difficulty speaking and ataxia.… (more)

Subjects/Keywords: Angelman; hippocampus; proteasome; UBE3A; Neurosciences

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APA (6th Edition):

Daily, J. L. (2012). Efficacy of Increased Ube3a Protein Levels in the Brain in Rescuing the Phenotype of an Angelman Syndrome Mouse. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/4305

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):

Daily, Jennifer L. “Efficacy of Increased Ube3a Protein Levels in the Brain in Rescuing the Phenotype of an Angelman Syndrome Mouse.” 2012. Thesis, University of South Florida. Accessed February 20, 2020. https://scholarcommons.usf.edu/etd/4305.

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

MLA Handbook (7th Edition):

Daily, Jennifer L. “Efficacy of Increased Ube3a Protein Levels in the Brain in Rescuing the Phenotype of an Angelman Syndrome Mouse.” 2012. Web. 20 Feb 2020.

Vancouver:

Daily JL. Efficacy of Increased Ube3a Protein Levels in the Brain in Rescuing the Phenotype of an Angelman Syndrome Mouse. [Internet] [Thesis]. University of South Florida; 2012. [cited 2020 Feb 20]. Available from: https://scholarcommons.usf.edu/etd/4305.

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

Council of Science Editors:

Daily JL. Efficacy of Increased Ube3a Protein Levels in the Brain in Rescuing the Phenotype of an Angelman Syndrome Mouse. [Thesis]. University of South Florida; 2012. Available from: https://scholarcommons.usf.edu/etd/4305

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


Vanderbilt University

11. Talley, Jennell Marie. Exploring the assembly and function of the telomerase accessory proteins Est1 and Est3 in Saccharomyces cerevisiae.

Degree: PhD, Biological Sciences, 2011, Vanderbilt University

 The work presented in this dissertation focuses on a how the telomerase complex assembles both in vivo and in vitro and begins to explore how… (more)

Subjects/Keywords: proteasome; TERT; cell cycle; Telomere

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APA (6th Edition):

Talley, J. M. (2011). Exploring the assembly and function of the telomerase accessory proteins Est1 and Est3 in Saccharomyces cerevisiae. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-07182011-134847/ ;

Chicago Manual of Style (16th Edition):

Talley, Jennell Marie. “Exploring the assembly and function of the telomerase accessory proteins Est1 and Est3 in Saccharomyces cerevisiae.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed February 20, 2020. http://etd.library.vanderbilt.edu/available/etd-07182011-134847/ ;.

MLA Handbook (7th Edition):

Talley, Jennell Marie. “Exploring the assembly and function of the telomerase accessory proteins Est1 and Est3 in Saccharomyces cerevisiae.” 2011. Web. 20 Feb 2020.

Vancouver:

Talley JM. Exploring the assembly and function of the telomerase accessory proteins Est1 and Est3 in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2020 Feb 20]. Available from: http://etd.library.vanderbilt.edu/available/etd-07182011-134847/ ;.

Council of Science Editors:

Talley JM. Exploring the assembly and function of the telomerase accessory proteins Est1 and Est3 in Saccharomyces cerevisiae. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://etd.library.vanderbilt.edu/available/etd-07182011-134847/ ;


University of Toronto

12. Wu, Edwin. The Role of Ubiquitin on Yeast Proteasome Dynamics in Quiescence.

Degree: 2013, University of Toronto

The ubiquitin-proteasome system regulates protein degradation. Although proteasomes localize in the nucleus of proliferating Saccharomyces cerevisiae, they are sequestered into cytoplasmic proteasome storage granules (PSG)… (more)

Subjects/Keywords: proteasome; ubiquitin; quiescence; 0487

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

APA (6th Edition):

Wu, E. (2013). The Role of Ubiquitin on Yeast Proteasome Dynamics in Quiescence. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/43342

Chicago Manual of Style (16th Edition):

Wu, Edwin. “The Role of Ubiquitin on Yeast Proteasome Dynamics in Quiescence.” 2013. Masters Thesis, University of Toronto. Accessed February 20, 2020. http://hdl.handle.net/1807/43342.

MLA Handbook (7th Edition):

Wu, Edwin. “The Role of Ubiquitin on Yeast Proteasome Dynamics in Quiescence.” 2013. Web. 20 Feb 2020.

Vancouver:

Wu E. The Role of Ubiquitin on Yeast Proteasome Dynamics in Quiescence. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2020 Feb 20]. Available from: http://hdl.handle.net/1807/43342.

Council of Science Editors:

Wu E. The Role of Ubiquitin on Yeast Proteasome Dynamics in Quiescence. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/43342


Harvard University

13. Bodnar, Nicholas. Mechanism and Structure of the Cdc48 ATPase Complex.

Degree: PhD, 2018, Harvard University

The yeast ATPase Cdc48 and its mammalian homolog p97 are essential proteins that use the energy of ATP hydrolysis to perform work on polypeptide substrates.… (more)

Subjects/Keywords: Cdc48/p97; ubiquitin-proteasome system

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APA (6th Edition):

Bodnar, N. (2018). Mechanism and Structure of the Cdc48 ATPase Complex. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:41127316

Chicago Manual of Style (16th Edition):

Bodnar, Nicholas. “Mechanism and Structure of the Cdc48 ATPase Complex.” 2018. Doctoral Dissertation, Harvard University. Accessed February 20, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:41127316.

MLA Handbook (7th Edition):

Bodnar, Nicholas. “Mechanism and Structure of the Cdc48 ATPase Complex.” 2018. Web. 20 Feb 2020.

Vancouver:

Bodnar N. Mechanism and Structure of the Cdc48 ATPase Complex. [Internet] [Doctoral dissertation]. Harvard University; 2018. [cited 2020 Feb 20]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:41127316.

Council of Science Editors:

Bodnar N. Mechanism and Structure of the Cdc48 ATPase Complex. [Doctoral Dissertation]. Harvard University; 2018. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:41127316


University of Texas – Austin

14. Bowen, Kimberly Elizabeth. Designing proteasome adaptors to deplete specific proteins from cells.

Degree: PhD, Cell and Molecular Biology, 2019, University of Texas – Austin

 Cellular protein levels are governed by their rates of synthesis and degradation, and both processes are intricately regulated. One way to study the role of… (more)

Subjects/Keywords: Proteasome; Degradation; Shp2; Abl

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APA (6th Edition):

Bowen, K. E. (2019). Designing proteasome adaptors to deplete specific proteins from cells. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2174

Chicago Manual of Style (16th Edition):

Bowen, Kimberly Elizabeth. “Designing proteasome adaptors to deplete specific proteins from cells.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed February 20, 2020. http://dx.doi.org/10.26153/tsw/2174.

MLA Handbook (7th Edition):

Bowen, Kimberly Elizabeth. “Designing proteasome adaptors to deplete specific proteins from cells.” 2019. Web. 20 Feb 2020.

Vancouver:

Bowen KE. Designing proteasome adaptors to deplete specific proteins from cells. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2020 Feb 20]. Available from: http://dx.doi.org/10.26153/tsw/2174.

Council of Science Editors:

Bowen KE. Designing proteasome adaptors to deplete specific proteins from cells. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/2174

15. Sherzai, Mursal. Investigating novel therapies for Friedreich's ataxia.

Degree: PhD, 2018, Brunel University

 Friedreich's ataxia (FRDA) is a progressive neurodegenerative disorder caused by a homozygous GAA repeat expansion mutation in intron 1 of the frataxin gene (FXN), which… (more)

Subjects/Keywords: Epigenetics; Proteasome inhibitors; HMTase inhibitors

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APA (6th Edition):

Sherzai, M. (2018). Investigating novel therapies for Friedreich's ataxia. (Doctoral Dissertation). Brunel University. Retrieved from http://bura.brunel.ac.uk/handle/2438/16971 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.765023

Chicago Manual of Style (16th Edition):

Sherzai, Mursal. “Investigating novel therapies for Friedreich's ataxia.” 2018. Doctoral Dissertation, Brunel University. Accessed February 20, 2020. http://bura.brunel.ac.uk/handle/2438/16971 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.765023.

MLA Handbook (7th Edition):

Sherzai, Mursal. “Investigating novel therapies for Friedreich's ataxia.” 2018. Web. 20 Feb 2020.

Vancouver:

Sherzai M. Investigating novel therapies for Friedreich's ataxia. [Internet] [Doctoral dissertation]. Brunel University; 2018. [cited 2020 Feb 20]. Available from: http://bura.brunel.ac.uk/handle/2438/16971 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.765023.

Council of Science Editors:

Sherzai M. Investigating novel therapies for Friedreich's ataxia. [Doctoral Dissertation]. Brunel University; 2018. Available from: http://bura.brunel.ac.uk/handle/2438/16971 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.765023


Georgia State University

16. Cacan, Ercan. Combating the Epigenome: Elucidation of Mechanisms Underlying Chemoresistance and Enhancing Tumor Immunogenicity.

Degree: PhD, Biology, 2015, Georgia State University

  Chemotherapy and radiation therapy remain the backbone of cancer treatments, and now cancer immunotherapy offers promising new approaches for the treatment of malignancies. One… (more)

Subjects/Keywords: Chemoresistance; Immunotherapy; Epigenetics; Radiation; Proteasome

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APA (6th Edition):

Cacan, E. (2015). Combating the Epigenome: Elucidation of Mechanisms Underlying Chemoresistance and Enhancing Tumor Immunogenicity. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/biology_diss/156

Chicago Manual of Style (16th Edition):

Cacan, Ercan. “Combating the Epigenome: Elucidation of Mechanisms Underlying Chemoresistance and Enhancing Tumor Immunogenicity.” 2015. Doctoral Dissertation, Georgia State University. Accessed February 20, 2020. https://scholarworks.gsu.edu/biology_diss/156.

MLA Handbook (7th Edition):

Cacan, Ercan. “Combating the Epigenome: Elucidation of Mechanisms Underlying Chemoresistance and Enhancing Tumor Immunogenicity.” 2015. Web. 20 Feb 2020.

Vancouver:

Cacan E. Combating the Epigenome: Elucidation of Mechanisms Underlying Chemoresistance and Enhancing Tumor Immunogenicity. [Internet] [Doctoral dissertation]. Georgia State University; 2015. [cited 2020 Feb 20]. Available from: https://scholarworks.gsu.edu/biology_diss/156.

Council of Science Editors:

Cacan E. Combating the Epigenome: Elucidation of Mechanisms Underlying Chemoresistance and Enhancing Tumor Immunogenicity. [Doctoral Dissertation]. Georgia State University; 2015. Available from: https://scholarworks.gsu.edu/biology_diss/156


IUPUI

17. Panfair, Dilrajkaur. Alternative Assembly Pathways of the 20S Proteasome and Non-canonical Complexes.

Degree: 2018, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

The 20S proteasome, a multi-subunit protease complex, present in all domains of life and some orders of bacteria, is involved… (more)

Subjects/Keywords: 20S Proteasome; Pathways; Assembly

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

APA (6th Edition):

Panfair, D. (2018). Alternative Assembly Pathways of the 20S Proteasome and Non-canonical Complexes. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/17952

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):

Panfair, Dilrajkaur. “Alternative Assembly Pathways of the 20S Proteasome and Non-canonical Complexes.” 2018. Thesis, IUPUI. Accessed February 20, 2020. http://hdl.handle.net/1805/17952.

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

MLA Handbook (7th Edition):

Panfair, Dilrajkaur. “Alternative Assembly Pathways of the 20S Proteasome and Non-canonical Complexes.” 2018. Web. 20 Feb 2020.

Vancouver:

Panfair D. Alternative Assembly Pathways of the 20S Proteasome and Non-canonical Complexes. [Internet] [Thesis]. IUPUI; 2018. [cited 2020 Feb 20]. Available from: http://hdl.handle.net/1805/17952.

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

Council of Science Editors:

Panfair D. Alternative Assembly Pathways of the 20S Proteasome and Non-canonical Complexes. [Thesis]. IUPUI; 2018. Available from: http://hdl.handle.net/1805/17952

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


University of Cambridge

18. Zhu, Ye. Studies on the autophagy gene WIPI4 and its interactor UBR5.

Degree: PhD, 2020, University of Cambridge

 Autophagy is a tightly regulated process that sequesters and delivers proteins and other cellular substances for degradation in the lysosome. Dysfunction of autophagy has been… (more)

Subjects/Keywords: autophagy; proteasome; neurodegeneration disease

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APA (6th Edition):

Zhu, Y. (2020). Studies on the autophagy gene WIPI4 and its interactor UBR5. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/300658

Chicago Manual of Style (16th Edition):

Zhu, Ye. “Studies on the autophagy gene WIPI4 and its interactor UBR5.” 2020. Doctoral Dissertation, University of Cambridge. Accessed February 20, 2020. https://www.repository.cam.ac.uk/handle/1810/300658.

MLA Handbook (7th Edition):

Zhu, Ye. “Studies on the autophagy gene WIPI4 and its interactor UBR5.” 2020. Web. 20 Feb 2020.

Vancouver:

Zhu Y. Studies on the autophagy gene WIPI4 and its interactor UBR5. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2020 Feb 20]. Available from: https://www.repository.cam.ac.uk/handle/1810/300658.

Council of Science Editors:

Zhu Y. Studies on the autophagy gene WIPI4 and its interactor UBR5. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/300658


University of Minnesota

19. Liu, Haiming. Understanding The Mechanisms Of Muscle Atrophy.

Degree: PhD, Rehabilitation Science, 2016, University of Minnesota

 Skeletal muscle mass is regulated by protein turnover, the balance between protein synthesis and degradation. Muscle atrophy or a loss of muscle mass occurs when… (more)

Subjects/Keywords: Frailty; Immunoproteasome; Muscle atrophy; Proteasome; Proteolysis; Ubiquitin-proteasome system

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APA (6th Edition):

Liu, H. (2016). Understanding The Mechanisms Of Muscle Atrophy. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/182315

Chicago Manual of Style (16th Edition):

Liu, Haiming. “Understanding The Mechanisms Of Muscle Atrophy.” 2016. Doctoral Dissertation, University of Minnesota. Accessed February 20, 2020. http://hdl.handle.net/11299/182315.

MLA Handbook (7th Edition):

Liu, Haiming. “Understanding The Mechanisms Of Muscle Atrophy.” 2016. Web. 20 Feb 2020.

Vancouver:

Liu H. Understanding The Mechanisms Of Muscle Atrophy. [Internet] [Doctoral dissertation]. University of Minnesota; 2016. [cited 2020 Feb 20]. Available from: http://hdl.handle.net/11299/182315.

Council of Science Editors:

Liu H. Understanding The Mechanisms Of Muscle Atrophy. [Doctoral Dissertation]. University of Minnesota; 2016. Available from: http://hdl.handle.net/11299/182315


Kansas State University

20. Wani, Prashant Sadanand. The role of proteasome specific chaperones and quality control in assembly of the proteasome.

Degree: PhD, Biochemistry and Molecular Biophysics, 2015, Kansas State University

 The proteasome is a large protease in the cell that contributes to the controlled degradation of proteins. This 2.5MDa 26S proteasome complex consists of a… (more)

Subjects/Keywords: Proteasome; Chaperones; Quality control; Proteasome assembly; Biochemistry (0487); Cellular Biology (0379)

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APA (6th Edition):

Wani, P. S. (2015). The role of proteasome specific chaperones and quality control in assembly of the proteasome. (Doctoral Dissertation). Kansas State University. Retrieved from http://hdl.handle.net/2097/20529

Chicago Manual of Style (16th Edition):

Wani, Prashant Sadanand. “The role of proteasome specific chaperones and quality control in assembly of the proteasome.” 2015. Doctoral Dissertation, Kansas State University. Accessed February 20, 2020. http://hdl.handle.net/2097/20529.

MLA Handbook (7th Edition):

Wani, Prashant Sadanand. “The role of proteasome specific chaperones and quality control in assembly of the proteasome.” 2015. Web. 20 Feb 2020.

Vancouver:

Wani PS. The role of proteasome specific chaperones and quality control in assembly of the proteasome. [Internet] [Doctoral dissertation]. Kansas State University; 2015. [cited 2020 Feb 20]. Available from: http://hdl.handle.net/2097/20529.

Council of Science Editors:

Wani PS. The role of proteasome specific chaperones and quality control in assembly of the proteasome. [Doctoral Dissertation]. Kansas State University; 2015. Available from: http://hdl.handle.net/2097/20529


Kansas State University

21. Vontz, Gabrielle Rae. Regulation of proteasome granule formation by proteasome shuttle factors.

Degree: MS, Department of Biology, 2019, Kansas State University

 Protein degradation is crucial for many cellular processes including cell cycle regulation, metabolism, and proteostasis. Proteasomes, essential complexes within cells, degrade short-lived and aberrant proteins… (more)

Subjects/Keywords: Proteasome; Shuttle factor; Proteasome granule; Rad23; Dsk2; Ddi1

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APA (6th Edition):

Vontz, G. R. (2019). Regulation of proteasome granule formation by proteasome shuttle factors. (Masters Thesis). Kansas State University. Retrieved from http://hdl.handle.net/2097/39654

Chicago Manual of Style (16th Edition):

Vontz, Gabrielle Rae. “Regulation of proteasome granule formation by proteasome shuttle factors.” 2019. Masters Thesis, Kansas State University. Accessed February 20, 2020. http://hdl.handle.net/2097/39654.

MLA Handbook (7th Edition):

Vontz, Gabrielle Rae. “Regulation of proteasome granule formation by proteasome shuttle factors.” 2019. Web. 20 Feb 2020.

Vancouver:

Vontz GR. Regulation of proteasome granule formation by proteasome shuttle factors. [Internet] [Masters thesis]. Kansas State University; 2019. [cited 2020 Feb 20]. Available from: http://hdl.handle.net/2097/39654.

Council of Science Editors:

Vontz GR. Regulation of proteasome granule formation by proteasome shuttle factors. [Masters Thesis]. Kansas State University; 2019. Available from: http://hdl.handle.net/2097/39654


Freie Universität Berlin

22. Dreger, Henryk. Molecular mechanisms responsible for the protective effects of proteasome inhibitors in the cardiovascular system.

Degree: 2013, Freie Universität Berlin

 The ubiquitin-proteasome-system (UPS) is the major protein degradation mechanism in eukaryotic cells responsible for the degradation of misfolded and aged proteins. Through regulated degradation of… (more)

Subjects/Keywords: proteasome; proteasome inhibitors; ubiquitin proteasome system; oxidative stress; epigenetics; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Dreger, H. (2013). Molecular mechanisms responsible for the protective effects of proteasome inhibitors in the cardiovascular system. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-7562

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):

Dreger, Henryk. “Molecular mechanisms responsible for the protective effects of proteasome inhibitors in the cardiovascular system.” 2013. Thesis, Freie Universität Berlin. Accessed February 20, 2020. http://dx.doi.org/10.17169/refubium-7562.

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

MLA Handbook (7th Edition):

Dreger, Henryk. “Molecular mechanisms responsible for the protective effects of proteasome inhibitors in the cardiovascular system.” 2013. Web. 20 Feb 2020.

Vancouver:

Dreger H. Molecular mechanisms responsible for the protective effects of proteasome inhibitors in the cardiovascular system. [Internet] [Thesis]. Freie Universität Berlin; 2013. [cited 2020 Feb 20]. Available from: http://dx.doi.org/10.17169/refubium-7562.

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

Council of Science Editors:

Dreger H. Molecular mechanisms responsible for the protective effects of proteasome inhibitors in the cardiovascular system. [Thesis]. Freie Universität Berlin; 2013. Available from: http://dx.doi.org/10.17169/refubium-7562

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

23. Carmony, Kimberly C. Elucidating Proteasome Catalytic Subunit Composition and Its Role in Proteasome Inhibitor Resistance.

Degree: 2016, University of Kentucky

Proteasome inhibitors bortezomib and carfilzomib are FDA-approved anticancer agents that have contributed to significant improvements in treatment outcomes. However, the eventual onset of acquired resistance… (more)

Subjects/Keywords: Proteasome Inhibitor; Bortezomib; Carfilzomib; Proteasome Subtype; Bifunctional Proteasome Probe; Biochemistry; Cancer Biology; Molecular Biology; Other Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Carmony, K. C. (2016). Elucidating Proteasome Catalytic Subunit Composition and Its Role in Proteasome Inhibitor Resistance. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacy_etds/56

Chicago Manual of Style (16th Edition):

Carmony, Kimberly C. “Elucidating Proteasome Catalytic Subunit Composition and Its Role in Proteasome Inhibitor Resistance.” 2016. Doctoral Dissertation, University of Kentucky. Accessed February 20, 2020. https://uknowledge.uky.edu/pharmacy_etds/56.

MLA Handbook (7th Edition):

Carmony, Kimberly C. “Elucidating Proteasome Catalytic Subunit Composition and Its Role in Proteasome Inhibitor Resistance.” 2016. Web. 20 Feb 2020.

Vancouver:

Carmony KC. Elucidating Proteasome Catalytic Subunit Composition and Its Role in Proteasome Inhibitor Resistance. [Internet] [Doctoral dissertation]. University of Kentucky; 2016. [cited 2020 Feb 20]. Available from: https://uknowledge.uky.edu/pharmacy_etds/56.

Council of Science Editors:

Carmony KC. Elucidating Proteasome Catalytic Subunit Composition and Its Role in Proteasome Inhibitor Resistance. [Doctoral Dissertation]. University of Kentucky; 2016. Available from: https://uknowledge.uky.edu/pharmacy_etds/56


University of Utah

24. Stadtmueller, Beth Marie. Structural studies of proteasome assembly chaperones and activator complexes.

Degree: PhD, Biochemistry, 2010, University of Utah

 This dissertation describes structural and biochemical studies on proteasome assembly chaperones and proteasome activator complexes. Chapters 1 and 2 provide a detailed introduction to proteasome(more)

Subjects/Keywords: Proteasome; Structural biology; Assembly chaperones; Activator complexes

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APA (6th Edition):

Stadtmueller, B. M. (2010). Structural studies of proteasome assembly chaperones and activator complexes. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/582/rec/2283

Chicago Manual of Style (16th Edition):

Stadtmueller, Beth Marie. “Structural studies of proteasome assembly chaperones and activator complexes.” 2010. Doctoral Dissertation, University of Utah. Accessed February 20, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/582/rec/2283.

MLA Handbook (7th Edition):

Stadtmueller, Beth Marie. “Structural studies of proteasome assembly chaperones and activator complexes.” 2010. Web. 20 Feb 2020.

Vancouver:

Stadtmueller BM. Structural studies of proteasome assembly chaperones and activator complexes. [Internet] [Doctoral dissertation]. University of Utah; 2010. [cited 2020 Feb 20]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/582/rec/2283.

Council of Science Editors:

Stadtmueller BM. Structural studies of proteasome assembly chaperones and activator complexes. [Doctoral Dissertation]. University of Utah; 2010. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/582/rec/2283

25. Bicev, Renata Naporano. Estudos estruturais de sistemas biológicos utilizando métodos de espalhamento.

Degree: Mestrado, Física, 2015, University of São Paulo

Neste trabalho serão apresentados resultados sobre três sistemas proteícos diferentes: Lisozima, Crioglobulina e Proteassomo, analisados a partir, principalmente, da técnica de espalhamento de Raios X… (more)

Subjects/Keywords: Proteasome; Proteassomo; Proteínas; Proteins; SAXS; SAXS

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APA (6th Edition):

Bicev, R. N. (2015). Estudos estruturais de sistemas biológicos utilizando métodos de espalhamento. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/43/43134/tde-06112015-131339/ ;

Chicago Manual of Style (16th Edition):

Bicev, Renata Naporano. “Estudos estruturais de sistemas biológicos utilizando métodos de espalhamento.” 2015. Masters Thesis, University of São Paulo. Accessed February 20, 2020. http://www.teses.usp.br/teses/disponiveis/43/43134/tde-06112015-131339/ ;.

MLA Handbook (7th Edition):

Bicev, Renata Naporano. “Estudos estruturais de sistemas biológicos utilizando métodos de espalhamento.” 2015. Web. 20 Feb 2020.

Vancouver:

Bicev RN. Estudos estruturais de sistemas biológicos utilizando métodos de espalhamento. [Internet] [Masters thesis]. University of São Paulo; 2015. [cited 2020 Feb 20]. Available from: http://www.teses.usp.br/teses/disponiveis/43/43134/tde-06112015-131339/ ;.

Council of Science Editors:

Bicev RN. Estudos estruturais de sistemas biológicos utilizando métodos de espalhamento. [Masters Thesis]. University of São Paulo; 2015. Available from: http://www.teses.usp.br/teses/disponiveis/43/43134/tde-06112015-131339/ ;


Texas A&M University

26. Harshbarger, Wayne. X-Ray Crystal Structure of Human 20s Proteasome in Complex with Carfilzomib.

Degree: 2015, Texas A&M University

 20S proteasomes are large, multicatalytic N- terminal threonine proteases which are tasked with maintaining intracellular homeostasis by the breaking down of mis-folded, oxidized, or tagged… (more)

Subjects/Keywords: 20S Proteasome; carfilzomib; multiple myeloma; cellular regulation

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APA (6th Edition):

Harshbarger, W. (2015). X-Ray Crystal Structure of Human 20s Proteasome in Complex with Carfilzomib. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/155004

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):

Harshbarger, Wayne. “X-Ray Crystal Structure of Human 20s Proteasome in Complex with Carfilzomib.” 2015. Thesis, Texas A&M University. Accessed February 20, 2020. http://hdl.handle.net/1969.1/155004.

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

MLA Handbook (7th Edition):

Harshbarger, Wayne. “X-Ray Crystal Structure of Human 20s Proteasome in Complex with Carfilzomib.” 2015. Web. 20 Feb 2020.

Vancouver:

Harshbarger W. X-Ray Crystal Structure of Human 20s Proteasome in Complex with Carfilzomib. [Internet] [Thesis]. Texas A&M University; 2015. [cited 2020 Feb 20]. Available from: http://hdl.handle.net/1969.1/155004.

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

Council of Science Editors:

Harshbarger W. X-Ray Crystal Structure of Human 20s Proteasome in Complex with Carfilzomib. [Thesis]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/155004

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


Penn State University

27. Reviriego Mendoza, Marta Maria. JC VIRUS LARGE T ANTIGEN INTERACTS WITH THE F-BOX PROTEIN b-TRANSDUCIN REPEAT CONTAINING PROTEIN (bTrCP), THEREBY INFLUENCING VIRAL DNA REPLICATION.

Degree: PhD, Biochemistry, Microbiology, and Molecular Biology, 2010, Penn State University

 JC virus (JCV) is a small DNA tumor virus that causes the fatal demyelinating disease progressive multifocal leucoencephalopathy (PML) in immunocompromised patients and has been… (more)

Subjects/Keywords: viral DNA replication; JC virus; proteasome; bTrCP

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APA (6th Edition):

Reviriego Mendoza, M. M. (2010). JC VIRUS LARGE T ANTIGEN INTERACTS WITH THE F-BOX PROTEIN b-TRANSDUCIN REPEAT CONTAINING PROTEIN (bTrCP), THEREBY INFLUENCING VIRAL DNA REPLICATION. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/11613

Chicago Manual of Style (16th Edition):

Reviriego Mendoza, Marta Maria. “JC VIRUS LARGE T ANTIGEN INTERACTS WITH THE F-BOX PROTEIN b-TRANSDUCIN REPEAT CONTAINING PROTEIN (bTrCP), THEREBY INFLUENCING VIRAL DNA REPLICATION.” 2010. Doctoral Dissertation, Penn State University. Accessed February 20, 2020. https://etda.libraries.psu.edu/catalog/11613.

MLA Handbook (7th Edition):

Reviriego Mendoza, Marta Maria. “JC VIRUS LARGE T ANTIGEN INTERACTS WITH THE F-BOX PROTEIN b-TRANSDUCIN REPEAT CONTAINING PROTEIN (bTrCP), THEREBY INFLUENCING VIRAL DNA REPLICATION.” 2010. Web. 20 Feb 2020.

Vancouver:

Reviriego Mendoza MM. JC VIRUS LARGE T ANTIGEN INTERACTS WITH THE F-BOX PROTEIN b-TRANSDUCIN REPEAT CONTAINING PROTEIN (bTrCP), THEREBY INFLUENCING VIRAL DNA REPLICATION. [Internet] [Doctoral dissertation]. Penn State University; 2010. [cited 2020 Feb 20]. Available from: https://etda.libraries.psu.edu/catalog/11613.

Council of Science Editors:

Reviriego Mendoza MM. JC VIRUS LARGE T ANTIGEN INTERACTS WITH THE F-BOX PROTEIN b-TRANSDUCIN REPEAT CONTAINING PROTEIN (bTrCP), THEREBY INFLUENCING VIRAL DNA REPLICATION. [Doctoral Dissertation]. Penn State University; 2010. Available from: https://etda.libraries.psu.edu/catalog/11613

28. Vigié, Pierre. Mitochondrial quality control : roles of autophagy, mitophagy and the proteasome : Contrôle qualité des mitochondries : rôles de l’autophagie, de la mitophagie et du protéasome.

Degree: Docteur es, Biochimie, 2018, Bordeaux

La mitophagie, la dégradation sélective des mitochondries par autophagie, est impliquée dans l’élimination des mitochondries endommagées ou superflues et requiert des régulateurs et protéines spécifiques.… (more)

Subjects/Keywords: Mitophagie; Autophagie; Protéasome; Mitophagy; Autophagy; Proteasome

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APA (6th Edition):

Vigié, P. (2018). Mitochondrial quality control : roles of autophagy, mitophagy and the proteasome : Contrôle qualité des mitochondries : rôles de l’autophagie, de la mitophagie et du protéasome. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2018BORD0202

Chicago Manual of Style (16th Edition):

Vigié, Pierre. “Mitochondrial quality control : roles of autophagy, mitophagy and the proteasome : Contrôle qualité des mitochondries : rôles de l’autophagie, de la mitophagie et du protéasome.” 2018. Doctoral Dissertation, Bordeaux. Accessed February 20, 2020. http://www.theses.fr/2018BORD0202.

MLA Handbook (7th Edition):

Vigié, Pierre. “Mitochondrial quality control : roles of autophagy, mitophagy and the proteasome : Contrôle qualité des mitochondries : rôles de l’autophagie, de la mitophagie et du protéasome.” 2018. Web. 20 Feb 2020.

Vancouver:

Vigié P. Mitochondrial quality control : roles of autophagy, mitophagy and the proteasome : Contrôle qualité des mitochondries : rôles de l’autophagie, de la mitophagie et du protéasome. [Internet] [Doctoral dissertation]. Bordeaux; 2018. [cited 2020 Feb 20]. Available from: http://www.theses.fr/2018BORD0202.

Council of Science Editors:

Vigié P. Mitochondrial quality control : roles of autophagy, mitophagy and the proteasome : Contrôle qualité des mitochondries : rôles de l’autophagie, de la mitophagie et du protéasome. [Doctoral Dissertation]. Bordeaux; 2018. Available from: http://www.theses.fr/2018BORD0202


University of Manchester

29. Lara González, Pablo. Investigating how the Spindle Assembly Checkpoint inhibits the onset of anaphase.

Degree: PhD, 2013, University of Manchester

 The Spindle Assembly Checkpoint (SAC) delays the onset of anaphase in response to unattached kinetochores. The mechanism by which the SAC works is by inhibiting… (more)

Subjects/Keywords: inhibitor; proteasome; ubiquitin; spindle assembly checkpoint; mitosis

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APA (6th Edition):

Lara González, P. (2013). Investigating how the Spindle Assembly Checkpoint inhibits the onset of anaphase. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/investigating-how-the-spindle-assembly-checkpoint-inhibits-the-onset-of-anaphase(91d10d3a-9fc9-4395-9a18-d29969d604f8).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764271

Chicago Manual of Style (16th Edition):

Lara González, Pablo. “Investigating how the Spindle Assembly Checkpoint inhibits the onset of anaphase.” 2013. Doctoral Dissertation, University of Manchester. Accessed February 20, 2020. https://www.research.manchester.ac.uk/portal/en/theses/investigating-how-the-spindle-assembly-checkpoint-inhibits-the-onset-of-anaphase(91d10d3a-9fc9-4395-9a18-d29969d604f8).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764271.

MLA Handbook (7th Edition):

Lara González, Pablo. “Investigating how the Spindle Assembly Checkpoint inhibits the onset of anaphase.” 2013. Web. 20 Feb 2020.

Vancouver:

Lara González P. Investigating how the Spindle Assembly Checkpoint inhibits the onset of anaphase. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2020 Feb 20]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/investigating-how-the-spindle-assembly-checkpoint-inhibits-the-onset-of-anaphase(91d10d3a-9fc9-4395-9a18-d29969d604f8).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764271.

Council of Science Editors:

Lara González P. Investigating how the Spindle Assembly Checkpoint inhibits the onset of anaphase. [Doctoral Dissertation]. University of Manchester; 2013. Available from: https://www.research.manchester.ac.uk/portal/en/theses/investigating-how-the-spindle-assembly-checkpoint-inhibits-the-onset-of-anaphase(91d10d3a-9fc9-4395-9a18-d29969d604f8).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764271

30. De La Mota-Peynado, Alina M. The role of the proteasome-associated protein Ecm29 in quality control of the proteasome.

Degree: PhD, Division of Biology, 2014, Kansas State University

 The ubiquitin-proteasome pathway is the major pathway of selective protein degradation in the cell. Disruption of this pathway affects cellular protein homeostasis and contributes to… (more)

Subjects/Keywords: Proteasome assembly; Ecm29; Molecular chaperones; Biology (0306)

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

APA (6th Edition):

De La Mota-Peynado, A. M. (2014). The role of the proteasome-associated protein Ecm29 in quality control of the proteasome. (Doctoral Dissertation). Kansas State University. Retrieved from http://hdl.handle.net/2097/18200

Chicago Manual of Style (16th Edition):

De La Mota-Peynado, Alina M. “The role of the proteasome-associated protein Ecm29 in quality control of the proteasome.” 2014. Doctoral Dissertation, Kansas State University. Accessed February 20, 2020. http://hdl.handle.net/2097/18200.

MLA Handbook (7th Edition):

De La Mota-Peynado, Alina M. “The role of the proteasome-associated protein Ecm29 in quality control of the proteasome.” 2014. Web. 20 Feb 2020.

Vancouver:

De La Mota-Peynado AM. The role of the proteasome-associated protein Ecm29 in quality control of the proteasome. [Internet] [Doctoral dissertation]. Kansas State University; 2014. [cited 2020 Feb 20]. Available from: http://hdl.handle.net/2097/18200.

Council of Science Editors:

De La Mota-Peynado AM. The role of the proteasome-associated protein Ecm29 in quality control of the proteasome. [Doctoral Dissertation]. Kansas State University; 2014. Available from: http://hdl.handle.net/2097/18200

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