Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(the ubiquitin proteasome pathway). Showing records 1 – 30 of 67556 total matches.

[1] [2] [3] [4] [5] … [2252]

Search Limiters

Last 2 Years | English Only

Degrees

Levels

Languages

Country

▼ Search Limiters


University of Illinois – Chicago

1. Yilun Sun (757143). Molecular Pathways for Repair of Topoisomerase II-Mediated DNA Damage.

Degree: 2017, University of Illinois – Chicago

 DNA Topoisomerases play an essential role in nuclear processes such as replication and transcription by managing the topology of DNA duplexes. Topoisomerase II (Top2) is… (more)

Subjects/Keywords: Uncategorized; Topoisomerase II; etoposide; DNA repair; MRE11; the ubiquitin-proteasome pathway; RNF4; UBAP2L; cancer chemotherapy

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

(757143), Y. S. (2017). Molecular Pathways for Repair of Topoisomerase II-Mediated DNA Damage. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/22215

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):

(757143), Yilun Sun. “Molecular Pathways for Repair of Topoisomerase II-Mediated DNA Damage.” 2017. Thesis, University of Illinois – Chicago. Accessed May 08, 2021. http://hdl.handle.net/10027/22215.

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

MLA Handbook (7th Edition):

(757143), Yilun Sun. “Molecular Pathways for Repair of Topoisomerase II-Mediated DNA Damage.” 2017. Web. 08 May 2021.

Vancouver:

(757143) YS. Molecular Pathways for Repair of Topoisomerase II-Mediated DNA Damage. [Internet] [Thesis]. University of Illinois – Chicago; 2017. [cited 2021 May 08]. Available from: http://hdl.handle.net/10027/22215.

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

Council of Science Editors:

(757143) YS. Molecular Pathways for Repair of Topoisomerase II-Mediated DNA Damage. [Thesis]. University of Illinois – Chicago; 2017. Available from: http://hdl.handle.net/10027/22215

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


Wayne State University

2. Schmitt, Sara M. Molecular Studies On The Anti-Tumor Effects Of Metal-Based Complexes: Involvement Of The Ubiquitin-Proteasome And Apoptotic Pathways.

Degree: PhD, Cancer Biology, 2014, Wayne State University

  The ubiquitin-proteasome pathway is crucial to normal cellular function, and as such, has been extensively investigated as a potential target for cancer therapeutics. Many… (more)

Subjects/Keywords: ALAD; Cancer; Metals; Ubiquitin-Proteasome Pathway; Molecular Biology; Oncology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Schmitt, S. M. (2014). Molecular Studies On The Anti-Tumor Effects Of Metal-Based Complexes: Involvement Of The Ubiquitin-Proteasome And Apoptotic Pathways. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/915

Chicago Manual of Style (16th Edition):

Schmitt, Sara M. “Molecular Studies On The Anti-Tumor Effects Of Metal-Based Complexes: Involvement Of The Ubiquitin-Proteasome And Apoptotic Pathways.” 2014. Doctoral Dissertation, Wayne State University. Accessed May 08, 2021. https://digitalcommons.wayne.edu/oa_dissertations/915.

MLA Handbook (7th Edition):

Schmitt, Sara M. “Molecular Studies On The Anti-Tumor Effects Of Metal-Based Complexes: Involvement Of The Ubiquitin-Proteasome And Apoptotic Pathways.” 2014. Web. 08 May 2021.

Vancouver:

Schmitt SM. Molecular Studies On The Anti-Tumor Effects Of Metal-Based Complexes: Involvement Of The Ubiquitin-Proteasome And Apoptotic Pathways. [Internet] [Doctoral dissertation]. Wayne State University; 2014. [cited 2021 May 08]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/915.

Council of Science Editors:

Schmitt SM. Molecular Studies On The Anti-Tumor Effects Of Metal-Based Complexes: Involvement Of The Ubiquitin-Proteasome And Apoptotic Pathways. [Doctoral Dissertation]. Wayne State University; 2014. Available from: https://digitalcommons.wayne.edu/oa_dissertations/915


Vanderbilt University

3. Nielsen, Casey Paulasue. Regulation of WNT pathway specification by DUB-E3 interactions.

Degree: PhD, Cell and Developmental Biology, 2019, Vanderbilt University

 The WNT signaling network is comprised of multiple receptors that relay various input signals via distinct transduction pathways to execute multiple complex and context-specific output… (more)

Subjects/Keywords: Ubiquitin proteasome system; Cell signaling; WNT pathway; ubiquitin rheostat; breast cancer cells; deubiquitylases

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Nielsen, C. P. (2019). Regulation of WNT pathway specification by DUB-E3 interactions. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13952

Chicago Manual of Style (16th Edition):

Nielsen, Casey Paulasue. “Regulation of WNT pathway specification by DUB-E3 interactions.” 2019. Doctoral Dissertation, Vanderbilt University. Accessed May 08, 2021. http://hdl.handle.net/1803/13952.

MLA Handbook (7th Edition):

Nielsen, Casey Paulasue. “Regulation of WNT pathway specification by DUB-E3 interactions.” 2019. Web. 08 May 2021.

Vancouver:

Nielsen CP. Regulation of WNT pathway specification by DUB-E3 interactions. [Internet] [Doctoral dissertation]. Vanderbilt University; 2019. [cited 2021 May 08]. Available from: http://hdl.handle.net/1803/13952.

Council of Science Editors:

Nielsen CP. Regulation of WNT pathway specification by DUB-E3 interactions. [Doctoral Dissertation]. Vanderbilt University; 2019. Available from: http://hdl.handle.net/1803/13952


University of Minnesota

4. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 May 08, 2021. http://hdl.handle.net/11299/162241.

MLA Handbook (7th Edition):

Randles, Leah Ann. “Defining how the 26S proteasome recognizes ubiquitinated substrates.” 2012. Web. 08 May 2021.

Vancouver:

Randles LA. Defining how the 26S proteasome recognizes ubiquitinated substrates. [Internet] [Doctoral dissertation]. University of Minnesota; 2012. [cited 2021 May 08]. 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

5. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 May 08, 2021. 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. 08 May 2021.

Vancouver:

Gonzales FR. Characterizing Postranslational Regulatory Mechanisms of the Ubiquitin Proteasome System. [Internet] [Thesis]. University of California – San Diego; 2017. [cited 2021 May 08]. 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

6. Sun, Penglin. Functional studies of S-RNase-based self-incompatibility in Petunia inflata.

Degree: 2015, Penn State University

 Many flowering plants possess self-incompatibility (SI), an intraspecific reproductive barrier by which pistils reject self-pollen to prevent inbreeding and accept non-self pollen to promote outcrossing.… (more)

Subjects/Keywords: Petunia inflata; self-incompatibility; S-RNase; S-locus F-box protein; ubiquitin-26S proteasome pathway; artificial microRNA

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sun, P. (2015). Functional studies of S-RNase-based self-incompatibility in Petunia inflata. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/24782

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):

Sun, Penglin. “Functional studies of S-RNase-based self-incompatibility in Petunia inflata.” 2015. Thesis, Penn State University. Accessed May 08, 2021. https://submit-etda.libraries.psu.edu/catalog/24782.

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

MLA Handbook (7th Edition):

Sun, Penglin. “Functional studies of S-RNase-based self-incompatibility in Petunia inflata.” 2015. Web. 08 May 2021.

Vancouver:

Sun P. Functional studies of S-RNase-based self-incompatibility in Petunia inflata. [Internet] [Thesis]. Penn State University; 2015. [cited 2021 May 08]. Available from: https://submit-etda.libraries.psu.edu/catalog/24782.

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

Council of Science Editors:

Sun P. Functional studies of S-RNase-based self-incompatibility in Petunia inflata. [Thesis]. Penn State University; 2015. Available from: https://submit-etda.libraries.psu.edu/catalog/24782

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


Penn State University

7. Srikanth, Abhinaya. Roles of CCR4-NOT in ubiquitination and the last resort mechanism of RNA polymerase II degradation.

Degree: 2016, Penn State University

 Several studies have explored the relationship between the cellular transcription machinery, the stress response mechanism and mRNA decay factors. Despite the identification of multiple factors… (more)

Subjects/Keywords: The Ccr4-Not complex; Ubiquitination; Ubiquitylation; RNA Polymerase II; proteasome-mediated degradation; last resort mechanism; Ubp3-Bre5; Not4; ubiquitin-proteasome

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Srikanth, A. (2016). Roles of CCR4-NOT in ubiquitination and the last resort mechanism of RNA polymerase II degradation. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/5x21tf405

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):

Srikanth, Abhinaya. “Roles of CCR4-NOT in ubiquitination and the last resort mechanism of RNA polymerase II degradation.” 2016. Thesis, Penn State University. Accessed May 08, 2021. https://submit-etda.libraries.psu.edu/catalog/5x21tf405.

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

MLA Handbook (7th Edition):

Srikanth, Abhinaya. “Roles of CCR4-NOT in ubiquitination and the last resort mechanism of RNA polymerase II degradation.” 2016. Web. 08 May 2021.

Vancouver:

Srikanth A. Roles of CCR4-NOT in ubiquitination and the last resort mechanism of RNA polymerase II degradation. [Internet] [Thesis]. Penn State University; 2016. [cited 2021 May 08]. Available from: https://submit-etda.libraries.psu.edu/catalog/5x21tf405.

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

Council of Science Editors:

Srikanth A. Roles of CCR4-NOT in ubiquitination and the last resort mechanism of RNA polymerase II degradation. [Thesis]. Penn State University; 2016. Available from: https://submit-etda.libraries.psu.edu/catalog/5x21tf405

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

8. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 May 08, 2021. 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. 08 May 2021.

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 2021 May 08]. 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

9. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 May 08, 2021. 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. 08 May 2021.

Vancouver:

Worden EJ. Structural and Functional Characterization of the Proteasomal Deubiquitinase Rpn11. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2021 May 08]. 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

10. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 May 08, 2021. 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. 08 May 2021.

Vancouver:

Mottet K. The poxvirus ubiquitin ligase p28 manipulates the ubiquitin proteasome system. [Internet] [Masters thesis]. University of Alberta; 2010. [cited 2021 May 08]. 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 Toronto

11. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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 May 08, 2021. http://hdl.handle.net/1807/43342.

MLA Handbook (7th Edition):

Wu, Edwin. “The Role of Ubiquitin on Yeast Proteasome Dynamics in Quiescence.” 2013. Web. 08 May 2021.

Vancouver:

Wu E. The Role of Ubiquitin on Yeast Proteasome Dynamics in Quiescence. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2021 May 08]. 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


Swedish University of Agricultural Sciences

12. Fahlén, Sara. Regulation of Myc oncoprotein function by E3 ubiquitin ligases.

Degree: 2008, Swedish University of Agricultural Sciences

 The Myc oncoprotein/transcription factor plays an important role in controlling cell proliferation, and is deregulated in many human cancers. Myc is a short-lived protein that… (more)

Subjects/Keywords: proteins; transcription; transcription factors; ligases; cell cycle; interferons; Myc; Skp2; Sug1; VHL; transcription; ubiquitin-proteasome pathway; cell cycle; cyclin E/Cdk2; p27Kip1; interferon-γ

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Fahlén, S. (2008). Regulation of Myc oncoprotein function by E3 ubiquitin ligases. (Doctoral Dissertation). Swedish University of Agricultural Sciences. Retrieved from http://pub.epsilon.slu.se/1897/

Chicago Manual of Style (16th Edition):

Fahlén, Sara. “Regulation of Myc oncoprotein function by E3 ubiquitin ligases.” 2008. Doctoral Dissertation, Swedish University of Agricultural Sciences. Accessed May 08, 2021. http://pub.epsilon.slu.se/1897/.

MLA Handbook (7th Edition):

Fahlén, Sara. “Regulation of Myc oncoprotein function by E3 ubiquitin ligases.” 2008. Web. 08 May 2021.

Vancouver:

Fahlén S. Regulation of Myc oncoprotein function by E3 ubiquitin ligases. [Internet] [Doctoral dissertation]. Swedish University of Agricultural Sciences; 2008. [cited 2021 May 08]. Available from: http://pub.epsilon.slu.se/1897/.

Council of Science Editors:

Fahlén S. Regulation of Myc oncoprotein function by E3 ubiquitin ligases. [Doctoral Dissertation]. Swedish University of Agricultural Sciences; 2008. Available from: http://pub.epsilon.slu.se/1897/


University of Michigan

13. Calderon, Marlene Sayoc. Electrical stimulation of denervated skeletal muscles of rats: Maintenance of contractile proteins and effect on the ubiquitin -proteasome pathway.

Degree: PhD, Molecular biology, 2002, University of Michigan

 Following one month of denervation, a skeletal muscle loses 62% of its mass and 95% of its maximum force. An optimized electrical stimulation protocol that… (more)

Subjects/Keywords: Contractile Proteins; Denervated; Effect; Electrical Stimulation; Maintenance; Rats; Skeletal Muscles; Ubiquitin-proteasome Pathway

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Calderon, M. S. (2002). Electrical stimulation of denervated skeletal muscles of rats: Maintenance of contractile proteins and effect on the ubiquitin -proteasome pathway. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/123139

Chicago Manual of Style (16th Edition):

Calderon, Marlene Sayoc. “Electrical stimulation of denervated skeletal muscles of rats: Maintenance of contractile proteins and effect on the ubiquitin -proteasome pathway.” 2002. Doctoral Dissertation, University of Michigan. Accessed May 08, 2021. http://hdl.handle.net/2027.42/123139.

MLA Handbook (7th Edition):

Calderon, Marlene Sayoc. “Electrical stimulation of denervated skeletal muscles of rats: Maintenance of contractile proteins and effect on the ubiquitin -proteasome pathway.” 2002. Web. 08 May 2021.

Vancouver:

Calderon MS. Electrical stimulation of denervated skeletal muscles of rats: Maintenance of contractile proteins and effect on the ubiquitin -proteasome pathway. [Internet] [Doctoral dissertation]. University of Michigan; 2002. [cited 2021 May 08]. Available from: http://hdl.handle.net/2027.42/123139.

Council of Science Editors:

Calderon MS. Electrical stimulation of denervated skeletal muscles of rats: Maintenance of contractile proteins and effect on the ubiquitin -proteasome pathway. [Doctoral Dissertation]. University of Michigan; 2002. Available from: http://hdl.handle.net/2027.42/123139


Universidade de Brasília

14. Larissa da Costa Souza. Associação entre o proteassoma e o inibidor de protease BTCI : caracterização fisico-química e efeitos moleculares em células de câncer de mama (MCF-7).

Degree: 2010, Universidade de Brasília

Dietas ricas em leguminosas têm sido associadas à baixa incidência de câncer em populações humanas, sendo essas plantas, ricas em inibidores de proteases. O BTCI… (more)

Subjects/Keywords: vigna unguiculata; inibidor Bowman-Birk; via ubiquitina-proteassoma; câncer de mama; BIOLOGIA MOLECULAR; vigna unguiculata; Bowman-Birk inhibitor; ubiquitin-proteasome pathway; breast cancer

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Souza, L. d. C. (2010). Associação entre o proteassoma e o inibidor de protease BTCI : caracterização fisico-química e efeitos moleculares em células de câncer de mama (MCF-7). (Thesis). Universidade de Brasília. Retrieved from http://bdtd.bce.unb.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=6612

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):

Souza, Larissa da Costa. “Associação entre o proteassoma e o inibidor de protease BTCI : caracterização fisico-química e efeitos moleculares em células de câncer de mama (MCF-7).” 2010. Thesis, Universidade de Brasília. Accessed May 08, 2021. http://bdtd.bce.unb.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=6612.

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

MLA Handbook (7th Edition):

Souza, Larissa da Costa. “Associação entre o proteassoma e o inibidor de protease BTCI : caracterização fisico-química e efeitos moleculares em células de câncer de mama (MCF-7).” 2010. Web. 08 May 2021.

Vancouver:

Souza LdC. Associação entre o proteassoma e o inibidor de protease BTCI : caracterização fisico-química e efeitos moleculares em células de câncer de mama (MCF-7). [Internet] [Thesis]. Universidade de Brasília; 2010. [cited 2021 May 08]. Available from: http://bdtd.bce.unb.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=6612.

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

Council of Science Editors:

Souza LdC. Associação entre o proteassoma e o inibidor de protease BTCI : caracterização fisico-química e efeitos moleculares em células de câncer de mama (MCF-7). [Thesis]. Universidade de Brasília; 2010. Available from: http://bdtd.bce.unb.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=6612

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


University of Queensland

15. Muslim, Mohammed Dzaidenny. Molecular, cellular and functional characterisation of novel proteasomal proteins hDDI1 and hDDI2.

Degree: School of Medicine, 2012, University of Queensland

 The ubiquitin-proteasome system plays an important role in a wide variety of cellular processes including gene regulation, cell cycle and DNA damage sensing/repair. The degradation… (more)

Subjects/Keywords: Ubiquitin-proteasome pathway; hDDI1; hDDI2; DNA damage; p53; 060103 Cell Development, Proliferation and Death; 060109 Proteomics and Intermolecular Interactions (excl. Medical Proteomics); 060199 Biochemistry and Cell Biology not elsewhere classified

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Muslim, M. D. (2012). Molecular, cellular and functional characterisation of novel proteasomal proteins hDDI1 and hDDI2. (Thesis). University of Queensland. Retrieved from http://espace.library.uq.edu.au/view/UQ:283061

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):

Muslim, Mohammed Dzaidenny. “Molecular, cellular and functional characterisation of novel proteasomal proteins hDDI1 and hDDI2.” 2012. Thesis, University of Queensland. Accessed May 08, 2021. http://espace.library.uq.edu.au/view/UQ:283061.

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

MLA Handbook (7th Edition):

Muslim, Mohammed Dzaidenny. “Molecular, cellular and functional characterisation of novel proteasomal proteins hDDI1 and hDDI2.” 2012. Web. 08 May 2021.

Vancouver:

Muslim MD. Molecular, cellular and functional characterisation of novel proteasomal proteins hDDI1 and hDDI2. [Internet] [Thesis]. University of Queensland; 2012. [cited 2021 May 08]. Available from: http://espace.library.uq.edu.au/view/UQ:283061.

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

Council of Science Editors:

Muslim MD. Molecular, cellular and functional characterisation of novel proteasomal proteins hDDI1 and hDDI2. [Thesis]. University of Queensland; 2012. Available from: http://espace.library.uq.edu.au/view/UQ:283061

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

16. CHOY MING JU, MILLY. Investigation of The Role of The Ubiquitin Proteasome Pathway in Dengue Virus Life Cycle.

Degree: 2015, National University of Singapore

Subjects/Keywords: dengue virus; virus egress; Aedes aegypti; ubiquitin proteasome pathway; bortezomib; antiviral therapy

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

CHOY MING JU, M. (2015). Investigation of The Role of The Ubiquitin Proteasome Pathway in Dengue Virus Life Cycle. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/119252

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):

CHOY MING JU, MILLY. “Investigation of The Role of The Ubiquitin Proteasome Pathway in Dengue Virus Life Cycle.” 2015. Thesis, National University of Singapore. Accessed May 08, 2021. http://scholarbank.nus.edu.sg/handle/10635/119252.

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

MLA Handbook (7th Edition):

CHOY MING JU, MILLY. “Investigation of The Role of The Ubiquitin Proteasome Pathway in Dengue Virus Life Cycle.” 2015. Web. 08 May 2021.

Vancouver:

CHOY MING JU M. Investigation of The Role of The Ubiquitin Proteasome Pathway in Dengue Virus Life Cycle. [Internet] [Thesis]. National University of Singapore; 2015. [cited 2021 May 08]. Available from: http://scholarbank.nus.edu.sg/handle/10635/119252.

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

Council of Science Editors:

CHOY MING JU M. Investigation of The Role of The Ubiquitin Proteasome Pathway in Dengue Virus Life Cycle. [Thesis]. National University of Singapore; 2015. Available from: http://scholarbank.nus.edu.sg/handle/10635/119252

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

17. Vaiou, Maria. Μελέτη της σχέσης της οδού των νευροπεπτιδίων με την οδό ουβικουϊτίνης – πρωτεασώματος στο πολλαπλό μυέλωμα.

Degree: 2016, University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας

Purpose Bortezomib (BTZ) is used for the treatment of multiple myeloma (MM). However, a significant proportion of patients may be refractory to the drug. This… (more)

Subjects/Keywords: Πολλαπλό μυέλωμα; Οδός ουβικουιτίνης-πρωτεασώματος; Βορτεζομίμπη; Ενδοθηλίνη-1 (ΕΤ-1); Υποδοχέας ETBR; Multiple myeloma; Ubiquitin proteasome pathway; Bortezomib; Endothelin-1; ETBR receptor

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Vaiou, M. (2016). Μελέτη της σχέσης της οδού των νευροπεπτιδίων με την οδό ουβικουϊτίνης – πρωτεασώματος στο πολλαπλό μυέλωμα. (Thesis). University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας. Retrieved from http://hdl.handle.net/10442/hedi/39158

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):

Vaiou, Maria. “Μελέτη της σχέσης της οδού των νευροπεπτιδίων με την οδό ουβικουϊτίνης – πρωτεασώματος στο πολλαπλό μυέλωμα.” 2016. Thesis, University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας. Accessed May 08, 2021. http://hdl.handle.net/10442/hedi/39158.

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

MLA Handbook (7th Edition):

Vaiou, Maria. “Μελέτη της σχέσης της οδού των νευροπεπτιδίων με την οδό ουβικουϊτίνης – πρωτεασώματος στο πολλαπλό μυέλωμα.” 2016. Web. 08 May 2021.

Vancouver:

Vaiou M. Μελέτη της σχέσης της οδού των νευροπεπτιδίων με την οδό ουβικουϊτίνης – πρωτεασώματος στο πολλαπλό μυέλωμα. [Internet] [Thesis]. University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας; 2016. [cited 2021 May 08]. Available from: http://hdl.handle.net/10442/hedi/39158.

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

Council of Science Editors:

Vaiou M. Μελέτη της σχέσης της οδού των νευροπεπτιδίων με την οδό ουβικουϊτίνης – πρωτεασώματος στο πολλαπλό μυέλωμα. [Thesis]. University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας; 2016. Available from: http://hdl.handle.net/10442/hedi/39158

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


Vanderbilt University

18. Howard, Gregory Caleb. The role of the ubiquitin-proteasome system in Gcn4 target gene transcription.

Degree: PhD, Cell and Developmental Biology, 2016, Vanderbilt University

 The ubiquitin–proteasome system (UPS) influences gene transcription in multiple ways. One way in which the UPS impacts transcription centers on transcriptional activators, the function of… (more)

Subjects/Keywords: ubiquitin; proteasome; transcription; Gcn4; Cdc48; chromatin

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Howard, G. C. (2016). The role of the ubiquitin-proteasome system in Gcn4 target gene transcription. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14041

Chicago Manual of Style (16th Edition):

Howard, Gregory Caleb. “The role of the ubiquitin-proteasome system in Gcn4 target gene transcription.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed May 08, 2021. http://hdl.handle.net/1803/14041.

MLA Handbook (7th Edition):

Howard, Gregory Caleb. “The role of the ubiquitin-proteasome system in Gcn4 target gene transcription.” 2016. Web. 08 May 2021.

Vancouver:

Howard GC. The role of the ubiquitin-proteasome system in Gcn4 target gene transcription. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2021 May 08]. Available from: http://hdl.handle.net/1803/14041.

Council of Science Editors:

Howard GC. The role of the ubiquitin-proteasome system in Gcn4 target gene transcription. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/14041


University of Toronto

19. Gu, Zhu Chao (Jerry). Enrichment and Analysis of Proteasome Storage Granules.

Degree: 2016, University of Toronto

Ubiquitin-proteasome system (UPS) is a conserved eukaryotic pathway essential for the turn-over of short-lived or unwanted proteins, through the coordination of substrate ubiquitylation, and subsequent… (more)

Subjects/Keywords: enrichment; proteasome; PSG; quiescence; ubiquitin; yeast; 0487

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gu, Z. C. (. (2016). Enrichment and Analysis of Proteasome Storage Granules. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/92688

Chicago Manual of Style (16th Edition):

Gu, Zhu Chao (Jerry). “Enrichment and Analysis of Proteasome Storage Granules.” 2016. Masters Thesis, University of Toronto. Accessed May 08, 2021. http://hdl.handle.net/1807/92688.

MLA Handbook (7th Edition):

Gu, Zhu Chao (Jerry). “Enrichment and Analysis of Proteasome Storage Granules.” 2016. Web. 08 May 2021.

Vancouver:

Gu ZC(. Enrichment and Analysis of Proteasome Storage Granules. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2021 May 08]. Available from: http://hdl.handle.net/1807/92688.

Council of Science Editors:

Gu ZC(. Enrichment and Analysis of Proteasome Storage Granules. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/92688


University of Manchester

20. Lara González, Pablo. Investigating how the spindle assembly checkpoint inhibits the onset of anaphase.

Degree: 2012, 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: mitosis; spindle assembly checkpoint; ubiquitin; proteasome; inhibitor

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lara González, P. (2012). Investigating how the spindle assembly checkpoint inhibits the onset of anaphase. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:172728

Chicago Manual of Style (16th Edition):

Lara González, Pablo. “Investigating how the spindle assembly checkpoint inhibits the onset of anaphase.” 2012. Doctoral Dissertation, University of Manchester. Accessed May 08, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:172728.

MLA Handbook (7th Edition):

Lara González, Pablo. “Investigating how the spindle assembly checkpoint inhibits the onset of anaphase.” 2012. Web. 08 May 2021.

Vancouver:

Lara González P. Investigating how the spindle assembly checkpoint inhibits the onset of anaphase. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2021 May 08]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:172728.

Council of Science Editors:

Lara González P. Investigating how the spindle assembly checkpoint inhibits the onset of anaphase. [Doctoral Dissertation]. University of Manchester; 2012. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:172728


Georgia Tech

21. Tennant, Esther Paula. Interactions of the chaperones and components of UB system in the formation and propagation of the yeast prion [PSI+].

Degree: MS, Biology, 2005, Georgia Tech

 Three of the best-characterized prions of Saccharomyces cerevisiae are [PSI+], [URE3], and [PIN+]. This study focuses on the prions [PSI+] and [PIN+]. [PSI+] is the… (more)

Subjects/Keywords: Ubiquitin; Proteasome; Chaperones

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Tennant, E. P. (2005). Interactions of the chaperones and components of UB system in the formation and propagation of the yeast prion [PSI+]. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/7157

Chicago Manual of Style (16th Edition):

Tennant, Esther Paula. “Interactions of the chaperones and components of UB system in the formation and propagation of the yeast prion [PSI+].” 2005. Masters Thesis, Georgia Tech. Accessed May 08, 2021. http://hdl.handle.net/1853/7157.

MLA Handbook (7th Edition):

Tennant, Esther Paula. “Interactions of the chaperones and components of UB system in the formation and propagation of the yeast prion [PSI+].” 2005. Web. 08 May 2021.

Vancouver:

Tennant EP. Interactions of the chaperones and components of UB system in the formation and propagation of the yeast prion [PSI+]. [Internet] [Masters thesis]. Georgia Tech; 2005. [cited 2021 May 08]. Available from: http://hdl.handle.net/1853/7157.

Council of Science Editors:

Tennant EP. Interactions of the chaperones and components of UB system in the formation and propagation of the yeast prion [PSI+]. [Masters Thesis]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/7157


University of Minnesota

22. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 May 08, 2021. http://hdl.handle.net/11299/182315.

MLA Handbook (7th Edition):

Liu, Haiming. “Understanding The Mechanisms Of Muscle Atrophy.” 2016. Web. 08 May 2021.

Vancouver:

Liu H. Understanding The Mechanisms Of Muscle Atrophy. [Internet] [Doctoral dissertation]. University of Minnesota; 2016. [cited 2021 May 08]. 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


University of Toronto

23. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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 May 08, 2021. 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. 08 May 2021.

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 2021 May 08]. 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


University of Maryland

24. Nowicka, Urszula Krystyna. STRUCTURAL AND FUNCTIONAL STUDIES OF THE DNA DAMAGE-INDUCIBLE UBL-UBA PROTEIN DDI1.

Degree: Biochemistry, 2014, University of Maryland

 The ubiquitin-proteasome system plays an essential role in the biology of eukaryotes. Through turnover of short-lived proteins, it regulates vital processes such as cell cycle… (more)

Subjects/Keywords: Biochemistry; Ddi1; shuttle proteins; ubiquitin; ubiquitin-proteasome system

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Nowicka, U. K. (2014). STRUCTURAL AND FUNCTIONAL STUDIES OF THE DNA DAMAGE-INDUCIBLE UBL-UBA PROTEIN DDI1. (Thesis). University of Maryland. Retrieved from http://hdl.handle.net/1903/15277

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):

Nowicka, Urszula Krystyna. “STRUCTURAL AND FUNCTIONAL STUDIES OF THE DNA DAMAGE-INDUCIBLE UBL-UBA PROTEIN DDI1.” 2014. Thesis, University of Maryland. Accessed May 08, 2021. http://hdl.handle.net/1903/15277.

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

MLA Handbook (7th Edition):

Nowicka, Urszula Krystyna. “STRUCTURAL AND FUNCTIONAL STUDIES OF THE DNA DAMAGE-INDUCIBLE UBL-UBA PROTEIN DDI1.” 2014. Web. 08 May 2021.

Vancouver:

Nowicka UK. STRUCTURAL AND FUNCTIONAL STUDIES OF THE DNA DAMAGE-INDUCIBLE UBL-UBA PROTEIN DDI1. [Internet] [Thesis]. University of Maryland; 2014. [cited 2021 May 08]. Available from: http://hdl.handle.net/1903/15277.

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

Council of Science Editors:

Nowicka UK. STRUCTURAL AND FUNCTIONAL STUDIES OF THE DNA DAMAGE-INDUCIBLE UBL-UBA PROTEIN DDI1. [Thesis]. University of Maryland; 2014. Available from: http://hdl.handle.net/1903/15277

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

25. Poirson, Juline. Interactome des oncoprotéines E6 et E7 des HPV : du système ubiquitine-protéasome à la voie de signalisation Hippo : HPV E6 and E7 oncoproteins interactome : from the ubiquitin-proteasome system to the Hippo signaling pathway.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2016, Université de Strasbourg

Les papillomavirus humains (HPV) constituent l’archétype des virus à ADN oncogènes. Les HPV muqueux à haut risque (principalement HPV16) sont les principaux agents étiologiques du… (more)

Subjects/Keywords: Interaction protéique; HPV; E6; E7; Ubiquitine-protéasome système; PDZ; Voie Hippo; YAP; TAZ; GPCA; IRF3; E6AP; P53; Protein interaction; HPV; E6; E7; Ubiquitin-proteasome pathway; PDZ; Hippo pathway; YAP; TAZ; GPCA; IRF3; E6AP; P53; 579.2; 572.8; 616.99

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Poirson, J. (2016). Interactome des oncoprotéines E6 et E7 des HPV : du système ubiquitine-protéasome à la voie de signalisation Hippo : HPV E6 and E7 oncoproteins interactome : from the ubiquitin-proteasome system to the Hippo signaling pathway. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2016STRAJ052

Chicago Manual of Style (16th Edition):

Poirson, Juline. “Interactome des oncoprotéines E6 et E7 des HPV : du système ubiquitine-protéasome à la voie de signalisation Hippo : HPV E6 and E7 oncoproteins interactome : from the ubiquitin-proteasome system to the Hippo signaling pathway.” 2016. Doctoral Dissertation, Université de Strasbourg. Accessed May 08, 2021. http://www.theses.fr/2016STRAJ052.

MLA Handbook (7th Edition):

Poirson, Juline. “Interactome des oncoprotéines E6 et E7 des HPV : du système ubiquitine-protéasome à la voie de signalisation Hippo : HPV E6 and E7 oncoproteins interactome : from the ubiquitin-proteasome system to the Hippo signaling pathway.” 2016. Web. 08 May 2021.

Vancouver:

Poirson J. Interactome des oncoprotéines E6 et E7 des HPV : du système ubiquitine-protéasome à la voie de signalisation Hippo : HPV E6 and E7 oncoproteins interactome : from the ubiquitin-proteasome system to the Hippo signaling pathway. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2016. [cited 2021 May 08]. Available from: http://www.theses.fr/2016STRAJ052.

Council of Science Editors:

Poirson J. Interactome des oncoprotéines E6 et E7 des HPV : du système ubiquitine-protéasome à la voie de signalisation Hippo : HPV E6 and E7 oncoproteins interactome : from the ubiquitin-proteasome system to the Hippo signaling pathway. [Doctoral Dissertation]. Université de Strasbourg; 2016. Available from: http://www.theses.fr/2016STRAJ052


Purdue University

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

Degree: Department of Biology at IUPUI, 2020, Purdue University

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

Subjects/Keywords: Biochemistry; Molecular Biology; Proteasome; Assembly; Pathway

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Panfair, D. (2020). Alternative Assembly Pathways of the 20S Proteasome and Non-canonical Complexes. (Thesis). Purdue University. Retrieved from http://hdl.handle.net/10.25394/pgs.7427822.v1

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.” 2020. Thesis, Purdue University. Accessed May 08, 2021. http://hdl.handle.net/10.25394/pgs.7427822.v1.

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.” 2020. Web. 08 May 2021.

Vancouver:

Panfair D. Alternative Assembly Pathways of the 20S Proteasome and Non-canonical Complexes. [Internet] [Thesis]. Purdue University; 2020. [cited 2021 May 08]. Available from: http://hdl.handle.net/10.25394/pgs.7427822.v1.

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]. Purdue University; 2020. Available from: http://hdl.handle.net/10.25394/pgs.7427822.v1

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

27. Goslin, Kevin. Characterization of the Ubiquitin N-end Rule Pathway in Arabidopsis.

Degree: 2019, RIAN

 The control of intracellular protein homeostasis is essential for the ability of plants to grow under different physiological conditions, as well as respond to various… (more)

Subjects/Keywords: Ubiquitin N-end Rule Pathway; Arabidopsis

Page 1 Page 2 Page 3

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Goslin, K. (2019). Characterization of the Ubiquitin N-end Rule Pathway in Arabidopsis. (Thesis). RIAN. Retrieved from http://mural.maynoothuniversity.ie/10860/

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):

Goslin, Kevin. “Characterization of the Ubiquitin N-end Rule Pathway in Arabidopsis.” 2019. Thesis, RIAN. Accessed May 08, 2021. http://mural.maynoothuniversity.ie/10860/.

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

MLA Handbook (7th Edition):

Goslin, Kevin. “Characterization of the Ubiquitin N-end Rule Pathway in Arabidopsis.” 2019. Web. 08 May 2021.

Vancouver:

Goslin K. Characterization of the Ubiquitin N-end Rule Pathway in Arabidopsis. [Internet] [Thesis]. RIAN; 2019. [cited 2021 May 08]. Available from: http://mural.maynoothuniversity.ie/10860/.

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

Council of Science Editors:

Goslin K. Characterization of the Ubiquitin N-end Rule Pathway in Arabidopsis. [Thesis]. RIAN; 2019. Available from: http://mural.maynoothuniversity.ie/10860/

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

28. Lionnard, Loïc. Régulation de la stabilité de la protéine anti-apoptotique BCL2A1 : Regulation of the stability of the anti-apoptotic protein BCL2A1.

Degree: Docteur es, Biologie Santé, 2018, Montpellier

L’apoptose ou mort cellulaire programmée joue un rôle prépondérant dans l’homéostasie cellulaire. Ce processus est très finement régulé par les protéines de la famille BCL-2… (more)

Subjects/Keywords: Apoptose; Famille BCL-2; Ubiquitine-Proteasome; Apoptosis; BCL-2 family; Ubiquitin-Proteasome

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lionnard, L. (2018). Régulation de la stabilité de la protéine anti-apoptotique BCL2A1 : Regulation of the stability of the anti-apoptotic protein BCL2A1. (Doctoral Dissertation). Montpellier. Retrieved from http://www.theses.fr/2018MONTT003

Chicago Manual of Style (16th Edition):

Lionnard, Loïc. “Régulation de la stabilité de la protéine anti-apoptotique BCL2A1 : Regulation of the stability of the anti-apoptotic protein BCL2A1.” 2018. Doctoral Dissertation, Montpellier. Accessed May 08, 2021. http://www.theses.fr/2018MONTT003.

MLA Handbook (7th Edition):

Lionnard, Loïc. “Régulation de la stabilité de la protéine anti-apoptotique BCL2A1 : Regulation of the stability of the anti-apoptotic protein BCL2A1.” 2018. Web. 08 May 2021.

Vancouver:

Lionnard L. Régulation de la stabilité de la protéine anti-apoptotique BCL2A1 : Regulation of the stability of the anti-apoptotic protein BCL2A1. [Internet] [Doctoral dissertation]. Montpellier; 2018. [cited 2021 May 08]. Available from: http://www.theses.fr/2018MONTT003.

Council of Science Editors:

Lionnard L. Régulation de la stabilité de la protéine anti-apoptotique BCL2A1 : Regulation of the stability of the anti-apoptotic protein BCL2A1. [Doctoral Dissertation]. Montpellier; 2018. Available from: http://www.theses.fr/2018MONTT003


Freie Universität Berlin

29. Dan, Cristian Ioan. Immunoproteasome subunit LMP7-deficiency in initiation and progression of atherosclerosis.

Degree: 2021, Freie Universität Berlin

 Atherosclerosis is a chronic inflammatory vascular disease with significant contribution to global morbidity and mortality. In atherogenesis protein homeostasis is disturbed and the major intracellular… (more)

Subjects/Keywords: proteasome; LMP7; atherosclerosis; immunoproteasome; β5i; protein homeostasis; ubiquitin-proteasome-system; ddc:610

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Dan, C. I. (2021). Immunoproteasome subunit LMP7-deficiency in initiation and progression of atherosclerosis. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-28803

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):

Dan, Cristian Ioan. “Immunoproteasome subunit LMP7-deficiency in initiation and progression of atherosclerosis.” 2021. Thesis, Freie Universität Berlin. Accessed May 08, 2021. http://dx.doi.org/10.17169/refubium-28803.

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

MLA Handbook (7th Edition):

Dan, Cristian Ioan. “Immunoproteasome subunit LMP7-deficiency in initiation and progression of atherosclerosis.” 2021. Web. 08 May 2021.

Vancouver:

Dan CI. Immunoproteasome subunit LMP7-deficiency in initiation and progression of atherosclerosis. [Internet] [Thesis]. Freie Universität Berlin; 2021. [cited 2021 May 08]. Available from: http://dx.doi.org/10.17169/refubium-28803.

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

Council of Science Editors:

Dan CI. Immunoproteasome subunit LMP7-deficiency in initiation and progression of atherosclerosis. [Thesis]. Freie Universität Berlin; 2021. Available from: http://dx.doi.org/10.17169/refubium-28803

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


University of Toledo

30. Lozar, Olivia Mae. Does Proteasome Activity Impact Skeletal Muscle Hypertrophy?.

Degree: PhD, Exercise Science, 2019, University of Toledo

 The Ubiquitin-Proteasome System (UPS) is the primary machinery responsible for protein degradation within skeletal muscle. There is evidence to suggest that the proteasome is activated… (more)

Subjects/Keywords: Kinesiology; Biology; Skeletal muscle hypertrophy; proteasome; ubiquitin-proteasome; protein degradation; hypertrophy; MG132; MG-132

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lozar, O. M. (2019). Does Proteasome Activity Impact Skeletal Muscle Hypertrophy?. (Doctoral Dissertation). University of Toledo. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=toledo1576264202406223

Chicago Manual of Style (16th Edition):

Lozar, Olivia Mae. “Does Proteasome Activity Impact Skeletal Muscle Hypertrophy?.” 2019. Doctoral Dissertation, University of Toledo. Accessed May 08, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1576264202406223.

MLA Handbook (7th Edition):

Lozar, Olivia Mae. “Does Proteasome Activity Impact Skeletal Muscle Hypertrophy?.” 2019. Web. 08 May 2021.

Vancouver:

Lozar OM. Does Proteasome Activity Impact Skeletal Muscle Hypertrophy?. [Internet] [Doctoral dissertation]. University of Toledo; 2019. [cited 2021 May 08]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1576264202406223.

Council of Science Editors:

Lozar OM. Does Proteasome Activity Impact Skeletal Muscle Hypertrophy?. [Doctoral Dissertation]. University of Toledo; 2019. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1576264202406223

[1] [2] [3] [4] [5] … [2252]

.