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You searched for subject:(Ubiquitin). Showing records 1 – 30 of 786 total matches.

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University of Minnesota

1. 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 November 26, 2020. http://hdl.handle.net/11299/162241.

MLA Handbook (7th Edition):

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

Vancouver:

Randles LA. Defining how the 26S proteasome recognizes ubiquitinated substrates. [Internet] [Doctoral dissertation]. University of Minnesota; 2012. [cited 2020 Nov 26]. 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


University of California – San Diego

2. 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 November 26, 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. 26 Nov 2020.

Vancouver:

Gonzales FR. Characterizing Postranslational Regulatory Mechanisms of the Ubiquitin Proteasome System. [Internet] [Thesis]. University of California – San Diego; 2017. [cited 2020 Nov 26]. 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


Penn State University

3. Ellis, Christopher Ross. Simulation studies of the glycosylation code.

Degree: 2014, Penn State University

 This thesis reports computational studies that investigate the impact of protein- carbohydrate and protein-protein interactions upon protein structure and folding. The core of this thesis,… (more)

Subjects/Keywords: glycosylation; toluene; ubiquitin

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APA (6th Edition):

Ellis, C. R. (2014). Simulation studies of the glycosylation code. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/22562

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):

Ellis, Christopher Ross. “Simulation studies of the glycosylation code.” 2014. Thesis, Penn State University. Accessed November 26, 2020. https://submit-etda.libraries.psu.edu/catalog/22562.

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

MLA Handbook (7th Edition):

Ellis, Christopher Ross. “Simulation studies of the glycosylation code.” 2014. Web. 26 Nov 2020.

Vancouver:

Ellis CR. Simulation studies of the glycosylation code. [Internet] [Thesis]. Penn State University; 2014. [cited 2020 Nov 26]. Available from: https://submit-etda.libraries.psu.edu/catalog/22562.

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

Council of Science Editors:

Ellis CR. Simulation studies of the glycosylation code. [Thesis]. Penn State University; 2014. Available from: https://submit-etda.libraries.psu.edu/catalog/22562

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


University of Dundee

4. Leidecker, Orsolya. Investigating the response of the NEDD8 ubiquitin-like molecule to diverse stress conditions.

Degree: PhD, 2012, University of Dundee

 NEDD8 modification of proteins is extensively studied in the recent years, and the ubiquitin-like molecule has been shown to be involved in numerous signalling pathways.… (more)

Subjects/Keywords: 572; nedd8; ubiquitin

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APA (6th Edition):

Leidecker, O. (2012). Investigating the response of the NEDD8 ubiquitin-like molecule to diverse stress conditions. (Doctoral Dissertation). University of Dundee. Retrieved from https://discovery.dundee.ac.uk/en/studentTheses/f19d9441-9b48-448d-aa88-6dd2e7f4b5bf ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578873

Chicago Manual of Style (16th Edition):

Leidecker, Orsolya. “Investigating the response of the NEDD8 ubiquitin-like molecule to diverse stress conditions.” 2012. Doctoral Dissertation, University of Dundee. Accessed November 26, 2020. https://discovery.dundee.ac.uk/en/studentTheses/f19d9441-9b48-448d-aa88-6dd2e7f4b5bf ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578873.

MLA Handbook (7th Edition):

Leidecker, Orsolya. “Investigating the response of the NEDD8 ubiquitin-like molecule to diverse stress conditions.” 2012. Web. 26 Nov 2020.

Vancouver:

Leidecker O. Investigating the response of the NEDD8 ubiquitin-like molecule to diverse stress conditions. [Internet] [Doctoral dissertation]. University of Dundee; 2012. [cited 2020 Nov 26]. Available from: https://discovery.dundee.ac.uk/en/studentTheses/f19d9441-9b48-448d-aa88-6dd2e7f4b5bf ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578873.

Council of Science Editors:

Leidecker O. Investigating the response of the NEDD8 ubiquitin-like molecule to diverse stress conditions. [Doctoral Dissertation]. University of Dundee; 2012. Available from: https://discovery.dundee.ac.uk/en/studentTheses/f19d9441-9b48-448d-aa88-6dd2e7f4b5bf ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578873


Rutgers University

5. Sharma, Pragati, 1984-. A lysine desert protects sumo-targeted Ub ligases from auto-ubiquitination and proteolysis to maintain genome stability in yeast.

Degree: PhD, Biochemistry, 2015, Rutgers University

Post-translational modification by SUMO (Small Ubiquitin-like MOdifier) regulates the enzymatic activity, subcellular localization, and protein-protein interactions of modified target proteins. SUMO has also been implicated… (more)

Subjects/Keywords: Lysine; Ubiquitin; Yeast

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APA (6th Edition):

Sharma, Pragati, 1. (2015). A lysine desert protects sumo-targeted Ub ligases from auto-ubiquitination and proteolysis to maintain genome stability in yeast. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/46433/

Chicago Manual of Style (16th Edition):

Sharma, Pragati, 1984-. “A lysine desert protects sumo-targeted Ub ligases from auto-ubiquitination and proteolysis to maintain genome stability in yeast.” 2015. Doctoral Dissertation, Rutgers University. Accessed November 26, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/46433/.

MLA Handbook (7th Edition):

Sharma, Pragati, 1984-. “A lysine desert protects sumo-targeted Ub ligases from auto-ubiquitination and proteolysis to maintain genome stability in yeast.” 2015. Web. 26 Nov 2020.

Vancouver:

Sharma, Pragati 1. A lysine desert protects sumo-targeted Ub ligases from auto-ubiquitination and proteolysis to maintain genome stability in yeast. [Internet] [Doctoral dissertation]. Rutgers University; 2015. [cited 2020 Nov 26]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/46433/.

Council of Science Editors:

Sharma, Pragati 1. A lysine desert protects sumo-targeted Ub ligases from auto-ubiquitination and proteolysis to maintain genome stability in yeast. [Doctoral Dissertation]. Rutgers University; 2015. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/46433/


Ruhr Universität Bochum

6. Nöpel-Dünnebacke, Stefanie. Identifikation und Lokalisation peroxisomaler Proteine des Menschen.

Degree: 2010, Ruhr Universität Bochum

 Problem Weitere Aufklärung der in Teilschritten ungeklärten Peroxisomenbiogenese durch Lokalisation von vierputativ peroxisomalen Proteinen in humanen Fibroblasten. Methode Immunfluoreszenzanalysen der GF-Fusionsproteine in humanen Fibroblasten und… (more)

Subjects/Keywords: Peroxisom; Peroxisom / Biogenese; Ubiquitin; Fibroblast

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APA (6th Edition):

Nöpel-Dünnebacke, S. (2010). Identifikation und Lokalisation peroxisomaler Proteine des Menschen. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-29514

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):

Nöpel-Dünnebacke, Stefanie. “Identifikation und Lokalisation peroxisomaler Proteine des Menschen.” 2010. Thesis, Ruhr Universität Bochum. Accessed November 26, 2020. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-29514.

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

MLA Handbook (7th Edition):

Nöpel-Dünnebacke, Stefanie. “Identifikation und Lokalisation peroxisomaler Proteine des Menschen.” 2010. Web. 26 Nov 2020.

Vancouver:

Nöpel-Dünnebacke S. Identifikation und Lokalisation peroxisomaler Proteine des Menschen. [Internet] [Thesis]. Ruhr Universität Bochum; 2010. [cited 2020 Nov 26]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-29514.

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

Council of Science Editors:

Nöpel-Dünnebacke S. Identifikation und Lokalisation peroxisomaler Proteine des Menschen. [Thesis]. Ruhr Universität Bochum; 2010. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-29514

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

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 November 26, 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. 26 Nov 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 Nov 26]. 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 November 26, 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. 26 Nov 2020.

Vancouver:

Worden EJ. Structural and Functional Characterization of the Proteasomal Deubiquitinase Rpn11. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2020 Nov 26]. 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 Alberta

9. 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 November 26, 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. 26 Nov 2020.

Vancouver:

Mottet K. The poxvirus ubiquitin ligase p28 manipulates the ubiquitin proteasome system. [Internet] [Masters thesis]. University of Alberta; 2010. [cited 2020 Nov 26]. 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


Penn State University

10. Harrison, Megan Stasik. The Involvement of Ubiquitin in Parainfluenza Virus 5 Budding .

Degree: 2011, Penn State University

Ubiquitin has been implicated in the process of enveloped virus budding based primarily on findings with retroviruses. Ubiquitination of retroviral Gag proteins appears to be… (more)

Subjects/Keywords: virus budding; paramyxovirus; ubiquitin

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APA (6th Edition):

Harrison, M. S. (2011). The Involvement of Ubiquitin in Parainfluenza Virus 5 Budding . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/12118

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):

Harrison, Megan Stasik. “The Involvement of Ubiquitin in Parainfluenza Virus 5 Budding .” 2011. Thesis, Penn State University. Accessed November 26, 2020. https://submit-etda.libraries.psu.edu/catalog/12118.

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

MLA Handbook (7th Edition):

Harrison, Megan Stasik. “The Involvement of Ubiquitin in Parainfluenza Virus 5 Budding .” 2011. Web. 26 Nov 2020.

Vancouver:

Harrison MS. The Involvement of Ubiquitin in Parainfluenza Virus 5 Budding . [Internet] [Thesis]. Penn State University; 2011. [cited 2020 Nov 26]. Available from: https://submit-etda.libraries.psu.edu/catalog/12118.

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

Council of Science Editors:

Harrison MS. The Involvement of Ubiquitin in Parainfluenza Virus 5 Budding . [Thesis]. Penn State University; 2011. Available from: https://submit-etda.libraries.psu.edu/catalog/12118

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


Purdue University

11. Wade, Cameron. Biochemical Analysis of a Prokaryotic Deubiquitinase from Escherichia Coli.

Degree: MS, PULSe, 2016, Purdue University

 ElaD is a cysteine protease found in Escherichia coli (E. coli) and has been shown to function as a deubiquitinating enzyme (DUB). However, ubiquitin and… (more)

Subjects/Keywords: Bacteria; Deubiquitinase; Escherichia Coli; Ubiquitin

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

APA (6th Edition):

Wade, C. (2016). Biochemical Analysis of a Prokaryotic Deubiquitinase from Escherichia Coli. (Thesis). Purdue University. Retrieved from https://docs.lib.purdue.edu/open_access_theses/1233

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):

Wade, Cameron. “Biochemical Analysis of a Prokaryotic Deubiquitinase from Escherichia Coli.” 2016. Thesis, Purdue University. Accessed November 26, 2020. https://docs.lib.purdue.edu/open_access_theses/1233.

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

MLA Handbook (7th Edition):

Wade, Cameron. “Biochemical Analysis of a Prokaryotic Deubiquitinase from Escherichia Coli.” 2016. Web. 26 Nov 2020.

Vancouver:

Wade C. Biochemical Analysis of a Prokaryotic Deubiquitinase from Escherichia Coli. [Internet] [Thesis]. Purdue University; 2016. [cited 2020 Nov 26]. Available from: https://docs.lib.purdue.edu/open_access_theses/1233.

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

Council of Science Editors:

Wade C. Biochemical Analysis of a Prokaryotic Deubiquitinase from Escherichia Coli. [Thesis]. Purdue University; 2016. Available from: https://docs.lib.purdue.edu/open_access_theses/1233

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


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 (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 November 26, 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. 26 Nov 2020.

Vancouver:

Wu E. The Role of Ubiquitin on Yeast Proteasome Dynamics in Quiescence. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2020 Nov 26]. 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. Sievers, Quinlan. Modulation of the CRL4CRBN E3 Ubiquitin Ligase by Thalidomide Analogs.

Degree: PhD, 2017, Harvard University

Thalidomide and its derivatives, lenalidomide and pomalidomide, are effective therapies for the hematopoietic malignancies multiple myeloma and del(5q) myelodysplastic syndrome. Their therapeutic properties are a… (more)

Subjects/Keywords: thalidomide; ubiquitin ligase; cereblon

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APA (6th Edition):

Sievers, Q. (2017). Modulation of the CRL4CRBN E3 Ubiquitin Ligase by Thalidomide Analogs. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061478

Chicago Manual of Style (16th Edition):

Sievers, Quinlan. “Modulation of the CRL4CRBN E3 Ubiquitin Ligase by Thalidomide Analogs.” 2017. Doctoral Dissertation, Harvard University. Accessed November 26, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061478.

MLA Handbook (7th Edition):

Sievers, Quinlan. “Modulation of the CRL4CRBN E3 Ubiquitin Ligase by Thalidomide Analogs.” 2017. Web. 26 Nov 2020.

Vancouver:

Sievers Q. Modulation of the CRL4CRBN E3 Ubiquitin Ligase by Thalidomide Analogs. [Internet] [Doctoral dissertation]. Harvard University; 2017. [cited 2020 Nov 26]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061478.

Council of Science Editors:

Sievers Q. Modulation of the CRL4CRBN E3 Ubiquitin Ligase by Thalidomide Analogs. [Doctoral Dissertation]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061478


University of Adelaide

14. Khut, Poon-Yu. Structure function analysis of the deubiquitylating enzyme Fam.

Degree: 2006, University of Adelaide

 The ubiquitin pathway is a highly conserved post-translational modification system best characterised for its roles in protein degradation and intracellular trafficking and is involved in… (more)

Subjects/Keywords: ubiquitin; proteins

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APA (6th Edition):

Khut, P. (2006). Structure function analysis of the deubiquitylating enzyme Fam. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/59436

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):

Khut, Poon-Yu. “Structure function analysis of the deubiquitylating enzyme Fam.” 2006. Thesis, University of Adelaide. Accessed November 26, 2020. http://hdl.handle.net/2440/59436.

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

MLA Handbook (7th Edition):

Khut, Poon-Yu. “Structure function analysis of the deubiquitylating enzyme Fam.” 2006. Web. 26 Nov 2020.

Vancouver:

Khut P. Structure function analysis of the deubiquitylating enzyme Fam. [Internet] [Thesis]. University of Adelaide; 2006. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/2440/59436.

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

Council of Science Editors:

Khut P. Structure function analysis of the deubiquitylating enzyme Fam. [Thesis]. University of Adelaide; 2006. Available from: http://hdl.handle.net/2440/59436

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


University of Adelaide

15. Jolly, Lachlan. The deubiquitylating enzyme USP9X promotes the polarity and self-renewal of neural progenitor cells.

Degree: 2010, University of Adelaide

 Neural Progenitor Cells (NPCs) are the primordial cells of central nervous system (CNS). Understanding how they are regulated benefits our knowledge of normal development, the… (more)

Subjects/Keywords: neurogenesis; ubiquitin; embryonic stem cell

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APA (6th Edition):

Jolly, L. (2010). The deubiquitylating enzyme USP9X promotes the polarity and self-renewal of neural progenitor cells. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/65477

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):

Jolly, Lachlan. “The deubiquitylating enzyme USP9X promotes the polarity and self-renewal of neural progenitor cells.” 2010. Thesis, University of Adelaide. Accessed November 26, 2020. http://hdl.handle.net/2440/65477.

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

MLA Handbook (7th Edition):

Jolly, Lachlan. “The deubiquitylating enzyme USP9X promotes the polarity and self-renewal of neural progenitor cells.” 2010. Web. 26 Nov 2020.

Vancouver:

Jolly L. The deubiquitylating enzyme USP9X promotes the polarity and self-renewal of neural progenitor cells. [Internet] [Thesis]. University of Adelaide; 2010. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/2440/65477.

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

Council of Science Editors:

Jolly L. The deubiquitylating enzyme USP9X promotes the polarity and self-renewal of neural progenitor cells. [Thesis]. University of Adelaide; 2010. Available from: http://hdl.handle.net/2440/65477

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

16. Shrestha, Amit. The Proteostasis Function of the Saccharomyces Cerevisiae Metacaspase Yca1 .

Degree: 2017, University of Ottawa

 In addition to apoptosis, metacapases function to regulate various other processes that promote and sustain life. For example, the Saccharomyces cerevisiae metacaspase Yca1 promotes cellular… (more)

Subjects/Keywords: Proteostasis; Metacaspase; Ubiquitin; Rsp5; Yca1

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APA (6th Edition):

Shrestha, A. (2017). The Proteostasis Function of the Saccharomyces Cerevisiae Metacaspase Yca1 . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/36661

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):

Shrestha, Amit. “The Proteostasis Function of the Saccharomyces Cerevisiae Metacaspase Yca1 .” 2017. Thesis, University of Ottawa. Accessed November 26, 2020. http://hdl.handle.net/10393/36661.

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

MLA Handbook (7th Edition):

Shrestha, Amit. “The Proteostasis Function of the Saccharomyces Cerevisiae Metacaspase Yca1 .” 2017. Web. 26 Nov 2020.

Vancouver:

Shrestha A. The Proteostasis Function of the Saccharomyces Cerevisiae Metacaspase Yca1 . [Internet] [Thesis]. University of Ottawa; 2017. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/10393/36661.

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

Council of Science Editors:

Shrestha A. The Proteostasis Function of the Saccharomyces Cerevisiae Metacaspase Yca1 . [Thesis]. University of Ottawa; 2017. Available from: http://hdl.handle.net/10393/36661

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


University of Miami

17. Parvatiyar, Kislay. Ubiquitin Dependent Regulation of Innate Antiviral Signaling.

Degree: PhD, Microbiology and Immunology (Medicine), 2010, University of Miami

  Induction of type I interferons by the transcription factors IRF3 and IRF7 is essential in the initiation of antiviral innate immunity. Activation of IRF3/7… (more)

Subjects/Keywords: Ubiquitin Editing Complex; Signal Transduction

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

APA (6th Edition):

Parvatiyar, K. (2010). Ubiquitin Dependent Regulation of Innate Antiviral Signaling. (Doctoral Dissertation). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_dissertations/651

Chicago Manual of Style (16th Edition):

Parvatiyar, Kislay. “Ubiquitin Dependent Regulation of Innate Antiviral Signaling.” 2010. Doctoral Dissertation, University of Miami. Accessed November 26, 2020. https://scholarlyrepository.miami.edu/oa_dissertations/651.

MLA Handbook (7th Edition):

Parvatiyar, Kislay. “Ubiquitin Dependent Regulation of Innate Antiviral Signaling.” 2010. Web. 26 Nov 2020.

Vancouver:

Parvatiyar K. Ubiquitin Dependent Regulation of Innate Antiviral Signaling. [Internet] [Doctoral dissertation]. University of Miami; 2010. [cited 2020 Nov 26]. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/651.

Council of Science Editors:

Parvatiyar K. Ubiquitin Dependent Regulation of Innate Antiviral Signaling. [Doctoral Dissertation]. University of Miami; 2010. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/651


Boston University

18. Lin, Amy Wei Pey. Regulation of glutamatergic AMPA receptor stability and trafficking by ubiquitination.

Degree: PhD, Neuroscience, 2013, Boston University

 AMPA-type glutamate receptors (AMPARs) play a critical role in mediating the majority of fast excitatory synaptic transmission in the brain, where alterations in receptor expression,… (more)

Subjects/Keywords: Neurosciences; AMPAR; Eps15; Trafficking; Ubiquitin

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

APA (6th Edition):

Lin, A. W. P. (2013). Regulation of glutamatergic AMPA receptor stability and trafficking by ubiquitination. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/13152

Chicago Manual of Style (16th Edition):

Lin, Amy Wei Pey. “Regulation of glutamatergic AMPA receptor stability and trafficking by ubiquitination.” 2013. Doctoral Dissertation, Boston University. Accessed November 26, 2020. http://hdl.handle.net/2144/13152.

MLA Handbook (7th Edition):

Lin, Amy Wei Pey. “Regulation of glutamatergic AMPA receptor stability and trafficking by ubiquitination.” 2013. Web. 26 Nov 2020.

Vancouver:

Lin AWP. Regulation of glutamatergic AMPA receptor stability and trafficking by ubiquitination. [Internet] [Doctoral dissertation]. Boston University; 2013. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/2144/13152.

Council of Science Editors:

Lin AWP. Regulation of glutamatergic AMPA receptor stability and trafficking by ubiquitination. [Doctoral Dissertation]. Boston University; 2013. Available from: http://hdl.handle.net/2144/13152


University of California – San Francisco

19. Hadjivassiliou, Haralambos Antonis. Mechanisms of pre-mRNA splicing in yeast.

Degree: Biochemistry and Molecular Biology, 2014, University of California – San Francisco

 The spliceosome is one of the cells largest and important molecular machines and yet it remains as one the least understood systems. This is a… (more)

Subjects/Keywords: Biochemistry; Biophysics; Sad1; spliceosome; ubiquitin

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APA (6th Edition):

Hadjivassiliou, H. A. (2014). Mechanisms of pre-mRNA splicing in yeast. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/2wj5816h

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):

Hadjivassiliou, Haralambos Antonis. “Mechanisms of pre-mRNA splicing in yeast.” 2014. Thesis, University of California – San Francisco. Accessed November 26, 2020. http://www.escholarship.org/uc/item/2wj5816h.

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

MLA Handbook (7th Edition):

Hadjivassiliou, Haralambos Antonis. “Mechanisms of pre-mRNA splicing in yeast.” 2014. Web. 26 Nov 2020.

Vancouver:

Hadjivassiliou HA. Mechanisms of pre-mRNA splicing in yeast. [Internet] [Thesis]. University of California – San Francisco; 2014. [cited 2020 Nov 26]. Available from: http://www.escholarship.org/uc/item/2wj5816h.

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

Council of Science Editors:

Hadjivassiliou HA. Mechanisms of pre-mRNA splicing in yeast. [Thesis]. University of California – San Francisco; 2014. Available from: http://www.escholarship.org/uc/item/2wj5816h

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


Universidad de Cantabria

20. Muñiz Diego, María del Carmen. The role of Smad Ubiquitin Regulatory Factor-1: SMURF1 in the differentiation 3T3-L1.

Degree: Máster en Biología Molecular y Biomedicina, 2013, Universidad de Cantabria

 The Smad Ubiquitin Regulatory Factor-1: SMURF1 is an E3 ligase. This E3 ligase has been linked to several important biological pathways, including the bone morphogenetic… (more)

Subjects/Keywords: Smad Ubiquitin Regulatory Factor-1

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

APA (6th Edition):

Muñiz Diego, M. d. C. (2013). The role of Smad Ubiquitin Regulatory Factor-1: SMURF1 in the differentiation 3T3-L1. (Masters Thesis). Universidad de Cantabria. Retrieved from http://hdl.handle.net/10902/4198

Chicago Manual of Style (16th Edition):

Muñiz Diego, María del Carmen. “The role of Smad Ubiquitin Regulatory Factor-1: SMURF1 in the differentiation 3T3-L1.” 2013. Masters Thesis, Universidad de Cantabria. Accessed November 26, 2020. http://hdl.handle.net/10902/4198.

MLA Handbook (7th Edition):

Muñiz Diego, María del Carmen. “The role of Smad Ubiquitin Regulatory Factor-1: SMURF1 in the differentiation 3T3-L1.” 2013. Web. 26 Nov 2020.

Vancouver:

Muñiz Diego MdC. The role of Smad Ubiquitin Regulatory Factor-1: SMURF1 in the differentiation 3T3-L1. [Internet] [Masters thesis]. Universidad de Cantabria; 2013. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/10902/4198.

Council of Science Editors:

Muñiz Diego MdC. The role of Smad Ubiquitin Regulatory Factor-1: SMURF1 in the differentiation 3T3-L1. [Masters Thesis]. Universidad de Cantabria; 2013. Available from: http://hdl.handle.net/10902/4198


University of Toronto

21. Pascoe, Natasha. Yeast Two-Hybrid is an Effective Platform for the Discovery of Novel Inhibitors of Human Deubiquitinases.

Degree: PhD, 2018, University of Toronto

 Deubiquitinating enzymes represent attractive therapeutic targets that can be leveraged towards the treatment of a variety of devastating human health disorders. This doctoral thesis recounts… (more)

Subjects/Keywords: Biologics; DUBs; Ubiquitin; Yeast; 0307

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APA (6th Edition):

Pascoe, N. (2018). Yeast Two-Hybrid is an Effective Platform for the Discovery of Novel Inhibitors of Human Deubiquitinases. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/89877

Chicago Manual of Style (16th Edition):

Pascoe, Natasha. “Yeast Two-Hybrid is an Effective Platform for the Discovery of Novel Inhibitors of Human Deubiquitinases.” 2018. Doctoral Dissertation, University of Toronto. Accessed November 26, 2020. http://hdl.handle.net/1807/89877.

MLA Handbook (7th Edition):

Pascoe, Natasha. “Yeast Two-Hybrid is an Effective Platform for the Discovery of Novel Inhibitors of Human Deubiquitinases.” 2018. Web. 26 Nov 2020.

Vancouver:

Pascoe N. Yeast Two-Hybrid is an Effective Platform for the Discovery of Novel Inhibitors of Human Deubiquitinases. [Internet] [Doctoral dissertation]. University of Toronto; 2018. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1807/89877.

Council of Science Editors:

Pascoe N. Yeast Two-Hybrid is an Effective Platform for the Discovery of Novel Inhibitors of Human Deubiquitinases. [Doctoral Dissertation]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/89877


University of Toronto

22. Heir, Pardeep. Regulation of Cellular Oxygen Sensing Pathways by VHL.

Degree: PhD, 2015, University of Toronto

Erythropoiesis represents a vital physiologic process that can be adjusted to combat compromised oxygen availability, otherwise known as hypoxia. The canonical response to adapt to… (more)

Subjects/Keywords: Erythropoiesis; Hypoxia; Ubiquitin; 0992

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APA (6th Edition):

Heir, P. (2015). Regulation of Cellular Oxygen Sensing Pathways by VHL. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/76677

Chicago Manual of Style (16th Edition):

Heir, Pardeep. “Regulation of Cellular Oxygen Sensing Pathways by VHL.” 2015. Doctoral Dissertation, University of Toronto. Accessed November 26, 2020. http://hdl.handle.net/1807/76677.

MLA Handbook (7th Edition):

Heir, Pardeep. “Regulation of Cellular Oxygen Sensing Pathways by VHL.” 2015. Web. 26 Nov 2020.

Vancouver:

Heir P. Regulation of Cellular Oxygen Sensing Pathways by VHL. [Internet] [Doctoral dissertation]. University of Toronto; 2015. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1807/76677.

Council of Science Editors:

Heir P. Regulation of Cellular Oxygen Sensing Pathways by VHL. [Doctoral Dissertation]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/76677


University of Arizona

23. Hart, Matthew Robert. Understanding EGFR Modification, Trafficking, and the Importance of its Juxtamembrane Domain in Cancer .

Degree: 2013, University of Arizona

 Much of what is known about the role of the ERBB family in cellular biology and in cancer has to do with canonical downstream signaling… (more)

Subjects/Keywords: EGFR; Peptide; Ubiquitin; Genetics; Cancer

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APA (6th Edition):

Hart, M. R. (2013). Understanding EGFR Modification, Trafficking, and the Importance of its Juxtamembrane Domain in Cancer . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/293476

Chicago Manual of Style (16th Edition):

Hart, Matthew Robert. “Understanding EGFR Modification, Trafficking, and the Importance of its Juxtamembrane Domain in Cancer .” 2013. Doctoral Dissertation, University of Arizona. Accessed November 26, 2020. http://hdl.handle.net/10150/293476.

MLA Handbook (7th Edition):

Hart, Matthew Robert. “Understanding EGFR Modification, Trafficking, and the Importance of its Juxtamembrane Domain in Cancer .” 2013. Web. 26 Nov 2020.

Vancouver:

Hart MR. Understanding EGFR Modification, Trafficking, and the Importance of its Juxtamembrane Domain in Cancer . [Internet] [Doctoral dissertation]. University of Arizona; 2013. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/10150/293476.

Council of Science Editors:

Hart MR. Understanding EGFR Modification, Trafficking, and the Importance of its Juxtamembrane Domain in Cancer . [Doctoral Dissertation]. University of Arizona; 2013. Available from: http://hdl.handle.net/10150/293476


University of Hong Kong

24. Hu, Xiaobin. The role of Uhrf1 in development and tumorigenesis.

Degree: 2014, University of Hong Kong

Subjects/Keywords: Ubiquitin; Carcinogenesis

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APA (6th Edition):

Hu, X. (2014). The role of Uhrf1 in development and tumorigenesis. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/225205

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):

Hu, Xiaobin. “The role of Uhrf1 in development and tumorigenesis.” 2014. Thesis, University of Hong Kong. Accessed November 26, 2020. http://hdl.handle.net/10722/225205.

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

MLA Handbook (7th Edition):

Hu, Xiaobin. “The role of Uhrf1 in development and tumorigenesis.” 2014. Web. 26 Nov 2020.

Vancouver:

Hu X. The role of Uhrf1 in development and tumorigenesis. [Internet] [Thesis]. University of Hong Kong; 2014. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/10722/225205.

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

Council of Science Editors:

Hu X. The role of Uhrf1 in development and tumorigenesis. [Thesis]. University of Hong Kong; 2014. Available from: http://hdl.handle.net/10722/225205

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


University of Maryland

25. Burke, Meghan Catherine. PROTEOMIC CHARACTERIZATION OF EXOSOMES SHED BY MYELOID-DERIVED SUPPRESSOR CELLS.

Degree: Biochemistry, 2015, University of Maryland

 Exosomes are a class of extracellular vesicles that have been shown to contribute to metastasis when derived from tumor cells. Myeloid-derived suppressor cells (MDSC) are… (more)

Subjects/Keywords: Biochemistry; Exosome; MDSC; Proteomics; Ubiquitin

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APA (6th Edition):

Burke, M. C. (2015). PROTEOMIC CHARACTERIZATION OF EXOSOMES SHED BY MYELOID-DERIVED SUPPRESSOR CELLS. (Thesis). University of Maryland. Retrieved from http://hdl.handle.net/1903/16973

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):

Burke, Meghan Catherine. “PROTEOMIC CHARACTERIZATION OF EXOSOMES SHED BY MYELOID-DERIVED SUPPRESSOR CELLS.” 2015. Thesis, University of Maryland. Accessed November 26, 2020. http://hdl.handle.net/1903/16973.

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

MLA Handbook (7th Edition):

Burke, Meghan Catherine. “PROTEOMIC CHARACTERIZATION OF EXOSOMES SHED BY MYELOID-DERIVED SUPPRESSOR CELLS.” 2015. Web. 26 Nov 2020.

Vancouver:

Burke MC. PROTEOMIC CHARACTERIZATION OF EXOSOMES SHED BY MYELOID-DERIVED SUPPRESSOR CELLS. [Internet] [Thesis]. University of Maryland; 2015. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1903/16973.

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

Council of Science Editors:

Burke MC. PROTEOMIC CHARACTERIZATION OF EXOSOMES SHED BY MYELOID-DERIVED SUPPRESSOR CELLS. [Thesis]. University of Maryland; 2015. Available from: http://hdl.handle.net/1903/16973

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


Virginia Tech

26. Mitra, Sharmistha. Ubiquitin Modulates Tollip's PtdIns(3)P Binding and Dissociates the Dimeric State of C-Terminal Cue Domain.

Degree: PhD, Biological Sciences, 2013, Virginia Tech

 Ubiquitylation is a highly controlled post-translational modification of proteins, in which proteins are conjugated either with monoubiquitin or polyubiquitin chains. Ubiquitin modifications on target proteins… (more)

Subjects/Keywords: Tollip; phosphoinositides; ubiquitin; endocytosis

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APA (6th Edition):

Mitra, S. (2013). Ubiquitin Modulates Tollip's PtdIns(3)P Binding and Dissociates the Dimeric State of C-Terminal Cue Domain. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/51151

Chicago Manual of Style (16th Edition):

Mitra, Sharmistha. “Ubiquitin Modulates Tollip's PtdIns(3)P Binding and Dissociates the Dimeric State of C-Terminal Cue Domain.” 2013. Doctoral Dissertation, Virginia Tech. Accessed November 26, 2020. http://hdl.handle.net/10919/51151.

MLA Handbook (7th Edition):

Mitra, Sharmistha. “Ubiquitin Modulates Tollip's PtdIns(3)P Binding and Dissociates the Dimeric State of C-Terminal Cue Domain.” 2013. Web. 26 Nov 2020.

Vancouver:

Mitra S. Ubiquitin Modulates Tollip's PtdIns(3)P Binding and Dissociates the Dimeric State of C-Terminal Cue Domain. [Internet] [Doctoral dissertation]. Virginia Tech; 2013. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/10919/51151.

Council of Science Editors:

Mitra S. Ubiquitin Modulates Tollip's PtdIns(3)P Binding and Dissociates the Dimeric State of C-Terminal Cue Domain. [Doctoral Dissertation]. Virginia Tech; 2013. Available from: http://hdl.handle.net/10919/51151


Loyola University Chicago

27. Staren, Daniel M. Characterization of the Coca Chemokine Receptor Four Agonist Activity of Ubiquitin.

Degree: MS, Molecular Biology, 2012, Loyola University Chicago

Ubiquitin has previously been identified as another natural agonist of CXC chemokine receptor 4 (CXCR4). In addition, recent evidence suggests that ubiquitin may activate… (more)

Subjects/Keywords: CXCR4; Ubiquitin; Molecular Biology

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APA (6th Edition):

Staren, D. M. (2012). Characterization of the Coca Chemokine Receptor Four Agonist Activity of Ubiquitin. (Thesis). Loyola University Chicago. Retrieved from https://ecommons.luc.edu/luc_theses/840

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):

Staren, Daniel M. “Characterization of the Coca Chemokine Receptor Four Agonist Activity of Ubiquitin.” 2012. Thesis, Loyola University Chicago. Accessed November 26, 2020. https://ecommons.luc.edu/luc_theses/840.

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

MLA Handbook (7th Edition):

Staren, Daniel M. “Characterization of the Coca Chemokine Receptor Four Agonist Activity of Ubiquitin.” 2012. Web. 26 Nov 2020.

Vancouver:

Staren DM. Characterization of the Coca Chemokine Receptor Four Agonist Activity of Ubiquitin. [Internet] [Thesis]. Loyola University Chicago; 2012. [cited 2020 Nov 26]. Available from: https://ecommons.luc.edu/luc_theses/840.

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

Council of Science Editors:

Staren DM. Characterization of the Coca Chemokine Receptor Four Agonist Activity of Ubiquitin. [Thesis]. Loyola University Chicago; 2012. Available from: https://ecommons.luc.edu/luc_theses/840

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


University of New South Wales

28. Shearer, Robert. Defining the role of the E3 ubiquitin ligase UBR5 in cancer.

Degree: Clinical School - St Vincent's Hospital, 2016, University of New South Wales

 Despite recent advances, breast cancer remains a major burden on the healthcare system in Australia and abroad. Of particular concern are cancer subtypes that currently… (more)

Subjects/Keywords: Ubiquitin; Cancer; Cilia; UBR5

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APA (6th Edition):

Shearer, R. (2016). Defining the role of the E3 ubiquitin ligase UBR5 in cancer. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/57120 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42626/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Shearer, Robert. “Defining the role of the E3 ubiquitin ligase UBR5 in cancer.” 2016. Doctoral Dissertation, University of New South Wales. Accessed November 26, 2020. http://handle.unsw.edu.au/1959.4/57120 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42626/SOURCE02?view=true.

MLA Handbook (7th Edition):

Shearer, Robert. “Defining the role of the E3 ubiquitin ligase UBR5 in cancer.” 2016. Web. 26 Nov 2020.

Vancouver:

Shearer R. Defining the role of the E3 ubiquitin ligase UBR5 in cancer. [Internet] [Doctoral dissertation]. University of New South Wales; 2016. [cited 2020 Nov 26]. Available from: http://handle.unsw.edu.au/1959.4/57120 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42626/SOURCE02?view=true.

Council of Science Editors:

Shearer R. Defining the role of the E3 ubiquitin ligase UBR5 in cancer. [Doctoral Dissertation]. University of New South Wales; 2016. Available from: http://handle.unsw.edu.au/1959.4/57120 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42626/SOURCE02?view=true


Texas Medical Center

29. Sirisaengtaksin, Natalie. CHARACTERIZATION OF THE UBIQUITIN LIGASE, UBE4B, IN ENDOCYTIC TRAFFICKING.

Degree: PhD, 2017, Texas Medical Center

  Endocytosis is a process by which cells internalize membrane proteins to remove them from the plasma membrane, allowing cells to regulate the cell surface… (more)

Subjects/Keywords: EGFR; UBE4B; ubiquitin; ubiquitin ligase; ESCRT; MVB; endosome; Biology; Cell Biology

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

APA (6th Edition):

Sirisaengtaksin, N. (2017). CHARACTERIZATION OF THE UBIQUITIN LIGASE, UBE4B, IN ENDOCYTIC TRAFFICKING. (Doctoral Dissertation). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/774

Chicago Manual of Style (16th Edition):

Sirisaengtaksin, Natalie. “CHARACTERIZATION OF THE UBIQUITIN LIGASE, UBE4B, IN ENDOCYTIC TRAFFICKING.” 2017. Doctoral Dissertation, Texas Medical Center. Accessed November 26, 2020. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/774.

MLA Handbook (7th Edition):

Sirisaengtaksin, Natalie. “CHARACTERIZATION OF THE UBIQUITIN LIGASE, UBE4B, IN ENDOCYTIC TRAFFICKING.” 2017. Web. 26 Nov 2020.

Vancouver:

Sirisaengtaksin N. CHARACTERIZATION OF THE UBIQUITIN LIGASE, UBE4B, IN ENDOCYTIC TRAFFICKING. [Internet] [Doctoral dissertation]. Texas Medical Center; 2017. [cited 2020 Nov 26]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/774.

Council of Science Editors:

Sirisaengtaksin N. CHARACTERIZATION OF THE UBIQUITIN LIGASE, UBE4B, IN ENDOCYTIC TRAFFICKING. [Doctoral Dissertation]. Texas Medical Center; 2017. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/774


University of Toronto

30. Halnin, Carlo de Guzman. Functional Analysis of the Contribution of HIF-1α Proline 402 to the Interaction with VHL.

Degree: 2016, University of Toronto

Hypoxia-inducible factor 1 alpha (HIF-1α) is involved in transcription of hypoxia-inducible genes. In normoxia, it binds von Hippel-Lindau (VHL) resulting in ubiquitin-proteasome degradation. This requires… (more)

Subjects/Keywords: E3 ubiquitin ligase; hypoxia-inducible factors; ubiquitin-proteasome degradation; 0307

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

APA (6th Edition):

Halnin, C. d. G. (2016). Functional Analysis of the Contribution of HIF-1α Proline 402 to the Interaction with VHL. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/74855

Chicago Manual of Style (16th Edition):

Halnin, Carlo de Guzman. “Functional Analysis of the Contribution of HIF-1α Proline 402 to the Interaction with VHL.” 2016. Masters Thesis, University of Toronto. Accessed November 26, 2020. http://hdl.handle.net/1807/74855.

MLA Handbook (7th Edition):

Halnin, Carlo de Guzman. “Functional Analysis of the Contribution of HIF-1α Proline 402 to the Interaction with VHL.” 2016. Web. 26 Nov 2020.

Vancouver:

Halnin CdG. Functional Analysis of the Contribution of HIF-1α Proline 402 to the Interaction with VHL. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1807/74855.

Council of Science Editors:

Halnin CdG. Functional Analysis of the Contribution of HIF-1α Proline 402 to the Interaction with VHL. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/74855

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