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You searched for subject:(Ubiquitin). Showing records 1 – 30 of 427 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 July 18, 2019. http://hdl.handle.net/11299/162241.

MLA Handbook (7th Edition):

Randles, Leah Ann. “Defining how the 26S proteasome recognizes ubiquitinated substrates.” 2012. Web. 18 Jul 2019.

Vancouver:

Randles LA. Defining how the 26S proteasome recognizes ubiquitinated substrates. [Internet] [Doctoral dissertation]. University of Minnesota; 2012. [cited 2019 Jul 18]. 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 Hong Kong

2. 王琳; Wang, Lin. The role of MDM2 in hepatic lipid metabolism.

Degree: Master of Medical Sciences, 2016, University of Hong Kong

 Background and objective: Liver is a core organ in regulation of lipid homeostasis, which is vital for life and health. Obesity is closely associated with… (more)

Subjects/Keywords: Ubiquitin; Lipids - Metabolism

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APA (6th Edition):

王琳; Wang, L. (2016). The role of MDM2 in hepatic lipid metabolism. (Masters Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/236279

Chicago Manual of Style (16th Edition):

王琳; Wang, Lin. “The role of MDM2 in hepatic lipid metabolism.” 2016. Masters Thesis, University of Hong Kong. Accessed July 18, 2019. http://hdl.handle.net/10722/236279.

MLA Handbook (7th Edition):

王琳; Wang, Lin. “The role of MDM2 in hepatic lipid metabolism.” 2016. Web. 18 Jul 2019.

Vancouver:

王琳; Wang L. The role of MDM2 in hepatic lipid metabolism. [Internet] [Masters thesis]. University of Hong Kong; 2016. [cited 2019 Jul 18]. Available from: http://hdl.handle.net/10722/236279.

Council of Science Editors:

王琳; Wang L. The role of MDM2 in hepatic lipid metabolism. [Masters Thesis]. University of Hong Kong; 2016. Available from: http://hdl.handle.net/10722/236279


University of Hong Kong

3. 成云; Cheng, Yun. β-TrCP-mediated ubiquitination and degradation of liver-enriched transcription factor CREB-H.

Degree: PhD, 2016, University of Hong Kong

 CREB-H is an endoplasmic reticulum-tethered bZIP transcription factor, which critically regulates lipid homeostasis and gluconeogenesis in the liver. CREB-H is proteolytically activated by regulated intramembrane… (more)

Subjects/Keywords: Transcription factors; Ubiquitin

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APA (6th Edition):

成云; Cheng, Y. (2016). β-TrCP-mediated ubiquitination and degradation of liver-enriched transcription factor CREB-H. (Doctoral Dissertation). University of Hong Kong. Retrieved from Cheng, Y. [成云]. (2016). β-TrCP-mediated ubiquitination and degradation of liver-enriched transcription factor CREB-H. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5816255. ; http://dx.doi.org/10.5353/th_b5816255 ; http://hdl.handle.net/10722/237862

Chicago Manual of Style (16th Edition):

成云; Cheng, Yun. “β-TrCP-mediated ubiquitination and degradation of liver-enriched transcription factor CREB-H.” 2016. Doctoral Dissertation, University of Hong Kong. Accessed July 18, 2019. Cheng, Y. [成云]. (2016). β-TrCP-mediated ubiquitination and degradation of liver-enriched transcription factor CREB-H. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5816255. ; http://dx.doi.org/10.5353/th_b5816255 ; http://hdl.handle.net/10722/237862.

MLA Handbook (7th Edition):

成云; Cheng, Yun. “β-TrCP-mediated ubiquitination and degradation of liver-enriched transcription factor CREB-H.” 2016. Web. 18 Jul 2019.

Vancouver:

成云; Cheng Y. β-TrCP-mediated ubiquitination and degradation of liver-enriched transcription factor CREB-H. [Internet] [Doctoral dissertation]. University of Hong Kong; 2016. [cited 2019 Jul 18]. Available from: Cheng, Y. [成云]. (2016). β-TrCP-mediated ubiquitination and degradation of liver-enriched transcription factor CREB-H. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5816255. ; http://dx.doi.org/10.5353/th_b5816255 ; http://hdl.handle.net/10722/237862.

Council of Science Editors:

成云; Cheng Y. β-TrCP-mediated ubiquitination and degradation of liver-enriched transcription factor CREB-H. [Doctoral Dissertation]. University of Hong Kong; 2016. Available from: Cheng, Y. [成云]. (2016). β-TrCP-mediated ubiquitination and degradation of liver-enriched transcription factor CREB-H. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5816255. ; http://dx.doi.org/10.5353/th_b5816255 ; http://hdl.handle.net/10722/237862


University of Hong Kong

4. Li, Tao. Structural and mechanistic insights into UHRF1-coordinated maintenance DNA methylation by DNMT1.

Degree: M. Phil., 2016, University of Hong Kong

DNA methylation is a crucial epigenetic modification and functions as a key factor in controlling gene expression and mammalian development. The DNA methyltransferase DNMT1 is… (more)

Subjects/Keywords: Ubiquitin; DNA - Methylation

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APA (6th Edition):

Li, T. (2016). Structural and mechanistic insights into UHRF1-coordinated maintenance DNA methylation by DNMT1. (Masters Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/240653

Chicago Manual of Style (16th Edition):

Li, Tao. “Structural and mechanistic insights into UHRF1-coordinated maintenance DNA methylation by DNMT1.” 2016. Masters Thesis, University of Hong Kong. Accessed July 18, 2019. http://hdl.handle.net/10722/240653.

MLA Handbook (7th Edition):

Li, Tao. “Structural and mechanistic insights into UHRF1-coordinated maintenance DNA methylation by DNMT1.” 2016. Web. 18 Jul 2019.

Vancouver:

Li T. Structural and mechanistic insights into UHRF1-coordinated maintenance DNA methylation by DNMT1. [Internet] [Masters thesis]. University of Hong Kong; 2016. [cited 2019 Jul 18]. Available from: http://hdl.handle.net/10722/240653.

Council of Science Editors:

Li T. Structural and mechanistic insights into UHRF1-coordinated maintenance DNA methylation by DNMT1. [Masters Thesis]. University of Hong Kong; 2016. Available from: http://hdl.handle.net/10722/240653


University of Hong Kong

5. Ruan, Yafei. Investigating the regulation of UHRF1 in cell cycle.

Degree: Master of Medical Sciences, 2015, University of Hong Kong

UHRF1 is a multi-domain protein with multiple functions in mammalian cells including maintenance of DNA methylation, histone modification, DNA damage et al. UHRF1 itself also… (more)

Subjects/Keywords: Cell cycle; Ubiquitin

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APA (6th Edition):

Ruan, Y. (2015). Investigating the regulation of UHRF1 in cell cycle. (Masters Thesis). University of Hong Kong. Retrieved from Ruan, Y. [阮雅菲]. (2015). Investigating the regulation of UHRF1 in cell cycle. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5659412 ; http://hdl.handle.net/10722/221484

Chicago Manual of Style (16th Edition):

Ruan, Yafei. “Investigating the regulation of UHRF1 in cell cycle.” 2015. Masters Thesis, University of Hong Kong. Accessed July 18, 2019. Ruan, Y. [阮雅菲]. (2015). Investigating the regulation of UHRF1 in cell cycle. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5659412 ; http://hdl.handle.net/10722/221484.

MLA Handbook (7th Edition):

Ruan, Yafei. “Investigating the regulation of UHRF1 in cell cycle.” 2015. Web. 18 Jul 2019.

Vancouver:

Ruan Y. Investigating the regulation of UHRF1 in cell cycle. [Internet] [Masters thesis]. University of Hong Kong; 2015. [cited 2019 Jul 18]. Available from: Ruan, Y. [阮雅菲]. (2015). Investigating the regulation of UHRF1 in cell cycle. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5659412 ; http://hdl.handle.net/10722/221484.

Council of Science Editors:

Ruan Y. Investigating the regulation of UHRF1 in cell cycle. [Masters Thesis]. University of Hong Kong; 2015. Available from: Ruan, Y. [阮雅菲]. (2015). Investigating the regulation of UHRF1 in cell cycle. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5659412 ; http://hdl.handle.net/10722/221484


University of Hong Kong

6. Tucker, Wesley Owen. Towards specific DNA aptamers which bind and inhibit WWP1 HECT ubiquitin ligase in the osteoblast.

Degree: PhD, 2013, University of Hong Kong

DNA aptamers have been studied since their inception in 1990, but have only targeted membrane and serum proteins in therapeutics. Their potential as inhibitors of… (more)

Subjects/Keywords: Ubiquitin; Osteoblasts; Oligonucleotides

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APA (6th Edition):

Tucker, W. O. (2013). Towards specific DNA aptamers which bind and inhibit WWP1 HECT ubiquitin ligase in the osteoblast. (Doctoral Dissertation). University of Hong Kong. Retrieved from Tucker, W. O.. (2013). Towards specific DNA aptamers which bind and inhibit WWP1 HECT ubiquitin ligase in the osteoblast. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5108666 ; http://dx.doi.org/10.5353/th_b5108666 ; http://hdl.handle.net/10722/205640

Chicago Manual of Style (16th Edition):

Tucker, Wesley Owen. “Towards specific DNA aptamers which bind and inhibit WWP1 HECT ubiquitin ligase in the osteoblast.” 2013. Doctoral Dissertation, University of Hong Kong. Accessed July 18, 2019. Tucker, W. O.. (2013). Towards specific DNA aptamers which bind and inhibit WWP1 HECT ubiquitin ligase in the osteoblast. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5108666 ; http://dx.doi.org/10.5353/th_b5108666 ; http://hdl.handle.net/10722/205640.

MLA Handbook (7th Edition):

Tucker, Wesley Owen. “Towards specific DNA aptamers which bind and inhibit WWP1 HECT ubiquitin ligase in the osteoblast.” 2013. Web. 18 Jul 2019.

Vancouver:

Tucker WO. Towards specific DNA aptamers which bind and inhibit WWP1 HECT ubiquitin ligase in the osteoblast. [Internet] [Doctoral dissertation]. University of Hong Kong; 2013. [cited 2019 Jul 18]. Available from: Tucker, W. O.. (2013). Towards specific DNA aptamers which bind and inhibit WWP1 HECT ubiquitin ligase in the osteoblast. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5108666 ; http://dx.doi.org/10.5353/th_b5108666 ; http://hdl.handle.net/10722/205640.

Council of Science Editors:

Tucker WO. Towards specific DNA aptamers which bind and inhibit WWP1 HECT ubiquitin ligase in the osteoblast. [Doctoral Dissertation]. University of Hong Kong; 2013. Available from: Tucker, W. O.. (2013). Towards specific DNA aptamers which bind and inhibit WWP1 HECT ubiquitin ligase in the osteoblast. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5108666 ; http://dx.doi.org/10.5353/th_b5108666 ; http://hdl.handle.net/10722/205640


University of California – San Diego

7. 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 July 18, 2019. 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. 18 Jul 2019.

Vancouver:

Gonzales FR. Characterizing Postranslational Regulatory Mechanisms of the Ubiquitin Proteasome System. [Internet] [Thesis]. University of California – San Diego; 2017. [cited 2019 Jul 18]. Available from: http://www.escholarship.org/uc/item/6958j596.

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

Council of Science Editors:

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

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


University of Alberta

8. 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 July 18, 2019. 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. 18 Jul 2019.

Vancouver:

Mottet K. The poxvirus ubiquitin ligase p28 manipulates the ubiquitin proteasome system. [Internet] [Masters thesis]. University of Alberta; 2010. [cited 2019 Jul 18]. 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

9. 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 July 18, 2019. 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. 18 Jul 2019.

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 2019 Jul 18]. 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 Hong Kong

10. 胡晓斌; Hu, Xiaobin. The role of Uhrf1 in development and tumorigenesis.

Degree: PhD, 2014, University of Hong Kong

published_or_final_version

Biochemistry

Doctoral

Doctor of Philosophy

Subjects/Keywords: Ubiquitin; Carcinogenesis

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APA (6th Edition):

胡晓斌; Hu, X. (2014). The role of Uhrf1 in development and tumorigenesis. (Doctoral Dissertation). University of Hong Kong. Retrieved from Hu, X. [胡晓斌]. (2014). The role of Uhrf1 in development and tumorigenesis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5736666 ; http://hdl.handle.net/10722/225205

Chicago Manual of Style (16th Edition):

胡晓斌; Hu, Xiaobin. “The role of Uhrf1 in development and tumorigenesis.” 2014. Doctoral Dissertation, University of Hong Kong. Accessed July 18, 2019. Hu, X. [胡晓斌]. (2014). The role of Uhrf1 in development and tumorigenesis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5736666 ; http://hdl.handle.net/10722/225205.

MLA Handbook (7th Edition):

胡晓斌; Hu, Xiaobin. “The role of Uhrf1 in development and tumorigenesis.” 2014. Web. 18 Jul 2019.

Vancouver:

胡晓斌; Hu X. The role of Uhrf1 in development and tumorigenesis. [Internet] [Doctoral dissertation]. University of Hong Kong; 2014. [cited 2019 Jul 18]. Available from: Hu, X. [胡晓斌]. (2014). The role of Uhrf1 in development and tumorigenesis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5736666 ; http://hdl.handle.net/10722/225205.

Council of Science Editors:

胡晓斌; Hu X. The role of Uhrf1 in development and tumorigenesis. [Doctoral Dissertation]. University of Hong Kong; 2014. Available from: Hu, X. [胡晓斌]. (2014). The role of Uhrf1 in development and tumorigenesis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5736666 ; http://hdl.handle.net/10722/225205


University of Hong Kong

11. Tse, Ho-sum. Investigation of the impacts of Parkinson's-disease-associated mutations (193M and S18Y) on the structure of human ubiquitincarboxyl-terminal hydrolase L1.

Degree: PhD, 2013, University of Hong Kong

Ubiquitin carboxy-terminal hydrolase L1 (UCH-L1), a protein of 223 amino acids, is a member of deubiquitinating enzymes and it is one of the most abundant… (more)

Subjects/Keywords: Parkinson's disease.; Ubiquitin.; Hydrolases.

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APA (6th Edition):

Tse, H. (2013). Investigation of the impacts of Parkinson's-disease-associated mutations (193M and S18Y) on the structure of human ubiquitincarboxyl-terminal hydrolase L1. (Doctoral Dissertation). University of Hong Kong. Retrieved from Tse, H. [謝灝森]. (2013). Investigation of the impacts of Parkinson's-disease-associated mutations (193M and S18Y) on the structure of human ubiquitin carboxyl-terminal hydrolase L1. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4979938 ; http://dx.doi.org/10.5353/th_b4979938 ; http://hdl.handle.net/10722/181505

Chicago Manual of Style (16th Edition):

Tse, Ho-sum. “Investigation of the impacts of Parkinson's-disease-associated mutations (193M and S18Y) on the structure of human ubiquitincarboxyl-terminal hydrolase L1.” 2013. Doctoral Dissertation, University of Hong Kong. Accessed July 18, 2019. Tse, H. [謝灝森]. (2013). Investigation of the impacts of Parkinson's-disease-associated mutations (193M and S18Y) on the structure of human ubiquitin carboxyl-terminal hydrolase L1. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4979938 ; http://dx.doi.org/10.5353/th_b4979938 ; http://hdl.handle.net/10722/181505.

MLA Handbook (7th Edition):

Tse, Ho-sum. “Investigation of the impacts of Parkinson's-disease-associated mutations (193M and S18Y) on the structure of human ubiquitincarboxyl-terminal hydrolase L1.” 2013. Web. 18 Jul 2019.

Vancouver:

Tse H. Investigation of the impacts of Parkinson's-disease-associated mutations (193M and S18Y) on the structure of human ubiquitincarboxyl-terminal hydrolase L1. [Internet] [Doctoral dissertation]. University of Hong Kong; 2013. [cited 2019 Jul 18]. Available from: Tse, H. [謝灝森]. (2013). Investigation of the impacts of Parkinson's-disease-associated mutations (193M and S18Y) on the structure of human ubiquitin carboxyl-terminal hydrolase L1. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4979938 ; http://dx.doi.org/10.5353/th_b4979938 ; http://hdl.handle.net/10722/181505.

Council of Science Editors:

Tse H. Investigation of the impacts of Parkinson's-disease-associated mutations (193M and S18Y) on the structure of human ubiquitincarboxyl-terminal hydrolase L1. [Doctoral Dissertation]. University of Hong Kong; 2013. Available from: Tse, H. [謝灝森]. (2013). Investigation of the impacts of Parkinson's-disease-associated mutations (193M and S18Y) on the structure of human ubiquitin carboxyl-terminal hydrolase L1. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4979938 ; http://dx.doi.org/10.5353/th_b4979938 ; http://hdl.handle.net/10722/181505


University of California – Berkeley

12. 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 July 18, 2019. 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. 18 Jul 2019.

Vancouver:

Worden EJ. Structural and Functional Characterization of the Proteasomal Deubiquitinase Rpn11. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2019 Jul 18]. Available from: http://www.escholarship.org/uc/item/2138s3gn.

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

Council of Science Editors:

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

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


University of Ottawa

13. 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 July 18, 2019. 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. 18 Jul 2019.

Vancouver:

Shrestha A. The Proteostasis Function of the Saccharomyces Cerevisiae Metacaspase Yca1 . [Internet] [Thesis]. University of Ottawa; 2017. [cited 2019 Jul 18]. 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 Arizona

14. 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 July 18, 2019. 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. 18 Jul 2019.

Vancouver:

Hart MR. Understanding EGFR Modification, Trafficking, and the Importance of its Juxtamembrane Domain in Cancer . [Internet] [Doctoral dissertation]. University of Arizona; 2013. [cited 2019 Jul 18]. 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 Toronto

15. 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 July 18, 2019. http://hdl.handle.net/1807/43342.

MLA Handbook (7th Edition):

Wu, Edwin. “The Role of Ubiquitin on Yeast Proteasome Dynamics in Quiescence.” 2013. Web. 18 Jul 2019.

Vancouver:

Wu E. The Role of Ubiquitin on Yeast Proteasome Dynamics in Quiescence. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2019 Jul 18]. 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


Boston University

16. 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 (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 July 18, 2019. 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. 18 Jul 2019.

Vancouver:

Lin AWP. Regulation of glutamatergic AMPA receptor stability and trafficking by ubiquitination. [Internet] [Doctoral dissertation]. Boston University; 2013. [cited 2019 Jul 18]. 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 Rochester

17. Shen, Run; Chen, Di (1955 - ). Regulation of Runx2 protein stability in chondrocyte development.

Degree: PhD, 2009, University of Rochester

 During endochondral bone formation, cartilages provide the template for vascular invasion, which brings in osteoblasts to deposit bone matrix on the debris of apoptotic chondrocytes.… (more)

Subjects/Keywords: Ubiquitin; Runx2; Chondrocyte; PTHrP; Cartilage

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APA (6th Edition):

Shen, Run; Chen, D. (. -. ). (2009). Regulation of Runx2 protein stability in chondrocyte development. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/6536

Chicago Manual of Style (16th Edition):

Shen, Run; Chen, Di (1955 - ). “Regulation of Runx2 protein stability in chondrocyte development.” 2009. Doctoral Dissertation, University of Rochester. Accessed July 18, 2019. http://hdl.handle.net/1802/6536.

MLA Handbook (7th Edition):

Shen, Run; Chen, Di (1955 - ). “Regulation of Runx2 protein stability in chondrocyte development.” 2009. Web. 18 Jul 2019.

Vancouver:

Shen, Run; Chen D(-). Regulation of Runx2 protein stability in chondrocyte development. [Internet] [Doctoral dissertation]. University of Rochester; 2009. [cited 2019 Jul 18]. Available from: http://hdl.handle.net/1802/6536.

Council of Science Editors:

Shen, Run; Chen D(-). Regulation of Runx2 protein stability in chondrocyte development. [Doctoral Dissertation]. University of Rochester; 2009. Available from: http://hdl.handle.net/1802/6536


University of California – San Francisco

18. 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 July 18, 2019. 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. 18 Jul 2019.

Vancouver:

Hadjivassiliou HA. Mechanisms of pre-mRNA splicing in yeast. [Internet] [Thesis]. University of California – San Francisco; 2014. [cited 2019 Jul 18]. 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


University of New South Wales

19. 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

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 July 18, 2019. http://handle.unsw.edu.au/1959.4/57120.

MLA Handbook (7th Edition):

Shearer, Robert. “Defining the role of the E3 ubiquitin ligase UBR5 in cancer.” 2016. Web. 18 Jul 2019.

Vancouver:

Shearer R. Defining the role of the E3 ubiquitin ligase UBR5 in cancer. [Internet] [Doctoral dissertation]. University of New South Wales; 2016. [cited 2019 Jul 18]. Available from: http://handle.unsw.edu.au/1959.4/57120.

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


University of Texas Southwestern Medical Center

20. Özkan, Engin. Mechanistic Studies of the Activation of Ubiquitin-Conjugating Enzymes by Ring-Type Ubiquitin Ligases.

Degree: 2006, University of Texas Southwestern Medical Center

 Ubiquitination, modification with ubiquitin, is a post-translational regulation of proteins in eukaryotes. Ubiquitin-activating enzymes (E1) activate ubiquitin and form thioester linkages with ubiquitin, which are… (more)

Subjects/Keywords: Ubiquitin; Eukaryota; Ubiquitin-Activating Enzymes

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APA (6th Edition):

Özkan, E. (2006). Mechanistic Studies of the Activation of Ubiquitin-Conjugating Enzymes by Ring-Type Ubiquitin Ligases. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/735

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):

Özkan, Engin. “Mechanistic Studies of the Activation of Ubiquitin-Conjugating Enzymes by Ring-Type Ubiquitin Ligases.” 2006. Thesis, University of Texas Southwestern Medical Center. Accessed July 18, 2019. http://hdl.handle.net/2152.5/735.

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

MLA Handbook (7th Edition):

Özkan, Engin. “Mechanistic Studies of the Activation of Ubiquitin-Conjugating Enzymes by Ring-Type Ubiquitin Ligases.” 2006. Web. 18 Jul 2019.

Vancouver:

Özkan E. Mechanistic Studies of the Activation of Ubiquitin-Conjugating Enzymes by Ring-Type Ubiquitin Ligases. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2006. [cited 2019 Jul 18]. Available from: http://hdl.handle.net/2152.5/735.

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

Council of Science Editors:

Özkan E. Mechanistic Studies of the Activation of Ubiquitin-Conjugating Enzymes by Ring-Type Ubiquitin Ligases. [Thesis]. University of Texas Southwestern Medical Center; 2006. Available from: http://hdl.handle.net/2152.5/735

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

21. Deaton, Michelle Kay. Species Preference of Viral Deubiquitinating Proteases Toward ISG15 Through Structural and Enzymatic Characterization.

Degree: PhD, Chemistry and Biochemistry, 2015, U of Denver

  Proteases from the Ovarian Tumor domain (OTU) superfamily of deubiquitinating enzymes (DUBs) are expressed by a range of RNA viruses. Viral OTUs (vOTUs) are… (more)

Subjects/Keywords: Deubiquitinating protease; ISG15; Ubiquitin; vOTU; Biochemistry

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APA (6th Edition):

Deaton, M. K. (2015). Species Preference of Viral Deubiquitinating Proteases Toward ISG15 Through Structural and Enzymatic Characterization. (Doctoral Dissertation). U of Denver. Retrieved from https://digitalcommons.du.edu/etd/1395

Chicago Manual of Style (16th Edition):

Deaton, Michelle Kay. “Species Preference of Viral Deubiquitinating Proteases Toward ISG15 Through Structural and Enzymatic Characterization.” 2015. Doctoral Dissertation, U of Denver. Accessed July 18, 2019. https://digitalcommons.du.edu/etd/1395.

MLA Handbook (7th Edition):

Deaton, Michelle Kay. “Species Preference of Viral Deubiquitinating Proteases Toward ISG15 Through Structural and Enzymatic Characterization.” 2015. Web. 18 Jul 2019.

Vancouver:

Deaton MK. Species Preference of Viral Deubiquitinating Proteases Toward ISG15 Through Structural and Enzymatic Characterization. [Internet] [Doctoral dissertation]. U of Denver; 2015. [cited 2019 Jul 18]. Available from: https://digitalcommons.du.edu/etd/1395.

Council of Science Editors:

Deaton MK. Species Preference of Viral Deubiquitinating Proteases Toward ISG15 Through Structural and Enzymatic Characterization. [Doctoral Dissertation]. U of Denver; 2015. Available from: https://digitalcommons.du.edu/etd/1395

22. Sharma, Mrinal. Structural and functional consequences of alteration in ubiquitin; -.

Degree: Biochemistry, 2012, Maharaja Sayajirao University of Baroda

Available

Bibliography p.161-177

Advisors/Committee Members: Prabha, C Ratna.

Subjects/Keywords: functional consequences; ubiquitin

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APA (6th Edition):

Sharma, M. (2012). Structural and functional consequences of alteration in ubiquitin; -. (Thesis). Maharaja Sayajirao University of Baroda. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/34732

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):

Sharma, Mrinal. “Structural and functional consequences of alteration in ubiquitin; -.” 2012. Thesis, Maharaja Sayajirao University of Baroda. Accessed July 18, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/34732.

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

MLA Handbook (7th Edition):

Sharma, Mrinal. “Structural and functional consequences of alteration in ubiquitin; -.” 2012. Web. 18 Jul 2019.

Vancouver:

Sharma M. Structural and functional consequences of alteration in ubiquitin; -. [Internet] [Thesis]. Maharaja Sayajirao University of Baroda; 2012. [cited 2019 Jul 18]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/34732.

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

Council of Science Editors:

Sharma M. Structural and functional consequences of alteration in ubiquitin; -. [Thesis]. Maharaja Sayajirao University of Baroda; 2012. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/34732

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


University of Otago

23. Budhidarmo, Rhesa Prabowo. Regulation of the E3 Ligase Activity of Human Cellular Inhibitor of Apoptosis Proteins .

Degree: 2013, University of Otago

 Post-translational modifications serve to regulate the function, activity, abundance or cellular localisation of proteins in a dynamic and timely manner. One form of such modifications… (more)

Subjects/Keywords: protein; apoptosis; cell signalling; ubiquitin; RING

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APA (6th Edition):

Budhidarmo, R. P. (2013). Regulation of the E3 Ligase Activity of Human Cellular Inhibitor of Apoptosis Proteins . (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/4287

Chicago Manual of Style (16th Edition):

Budhidarmo, Rhesa Prabowo. “Regulation of the E3 Ligase Activity of Human Cellular Inhibitor of Apoptosis Proteins .” 2013. Doctoral Dissertation, University of Otago. Accessed July 18, 2019. http://hdl.handle.net/10523/4287.

MLA Handbook (7th Edition):

Budhidarmo, Rhesa Prabowo. “Regulation of the E3 Ligase Activity of Human Cellular Inhibitor of Apoptosis Proteins .” 2013. Web. 18 Jul 2019.

Vancouver:

Budhidarmo RP. Regulation of the E3 Ligase Activity of Human Cellular Inhibitor of Apoptosis Proteins . [Internet] [Doctoral dissertation]. University of Otago; 2013. [cited 2019 Jul 18]. Available from: http://hdl.handle.net/10523/4287.

Council of Science Editors:

Budhidarmo RP. Regulation of the E3 Ligase Activity of Human Cellular Inhibitor of Apoptosis Proteins . [Doctoral Dissertation]. University of Otago; 2013. Available from: http://hdl.handle.net/10523/4287


University of Western Australia

24. Louw, Alison. The functional characterisation of human RMND5 proteins in normal physiology and prostate cancer.

Degree: PhD, 2013, University of Western Australia

[Truncated abstract] RMND5A and RMND5B are highly homologous uncharacterised proteins named after their yeast orthologue, Required for Meiotic Nuclear Division 5 (RMD5), a RING domain-containing… (more)

Subjects/Keywords: Prostate cancer; RMNDS; NKX3.1; E3 ubiquitin ligase

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APA (6th Edition):

Louw, A. (2013). The functional characterisation of human RMND5 proteins in normal physiology and prostate cancer. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=35131&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Louw, Alison. “The functional characterisation of human RMND5 proteins in normal physiology and prostate cancer.” 2013. Doctoral Dissertation, University of Western Australia. Accessed July 18, 2019. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=35131&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Louw, Alison. “The functional characterisation of human RMND5 proteins in normal physiology and prostate cancer.” 2013. Web. 18 Jul 2019.

Vancouver:

Louw A. The functional characterisation of human RMND5 proteins in normal physiology and prostate cancer. [Internet] [Doctoral dissertation]. University of Western Australia; 2013. [cited 2019 Jul 18]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=35131&local_base=GEN01-INS01.

Council of Science Editors:

Louw A. The functional characterisation of human RMND5 proteins in normal physiology and prostate cancer. [Doctoral Dissertation]. University of Western Australia; 2013. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=35131&local_base=GEN01-INS01


Georgia Tech

25. 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

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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 July 18, 2019. 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. 18 Jul 2019.

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 2019 Jul 18]. 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


Hong Kong University of Science and Technology

26. Hu, Wenbao. TRIP-Br1 mediates degradation of multiple adenylyl cyclase isoforms by XIAP E3 ligase.

Degree: 2015, Hong Kong University of Science and Technology

 Adenylyl cyclases (ACs) catalyze conversion of ATP to cAMP, a second messenger of utmost importance that regulates a vast array of biological processes in all… (more)

Subjects/Keywords: Adenylate cyclase; Proteins; Metabolism; Ubiquitin; Ligases

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APA (6th Edition):

Hu, W. (2015). TRIP-Br1 mediates degradation of multiple adenylyl cyclase isoforms by XIAP E3 ligase. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1514880 ; http://repository.ust.hk/ir/bitstream/1783.1-80226/1/th_redirect.html

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

Chicago Manual of Style (16th Edition):

Hu, Wenbao. “TRIP-Br1 mediates degradation of multiple adenylyl cyclase isoforms by XIAP E3 ligase.” 2015. Thesis, Hong Kong University of Science and Technology. Accessed July 18, 2019. https://doi.org/10.14711/thesis-b1514880 ; http://repository.ust.hk/ir/bitstream/1783.1-80226/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Hu, Wenbao. “TRIP-Br1 mediates degradation of multiple adenylyl cyclase isoforms by XIAP E3 ligase.” 2015. Web. 18 Jul 2019.

Vancouver:

Hu W. TRIP-Br1 mediates degradation of multiple adenylyl cyclase isoforms by XIAP E3 ligase. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2015. [cited 2019 Jul 18]. Available from: https://doi.org/10.14711/thesis-b1514880 ; http://repository.ust.hk/ir/bitstream/1783.1-80226/1/th_redirect.html.

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

Council of Science Editors:

Hu W. TRIP-Br1 mediates degradation of multiple adenylyl cyclase isoforms by XIAP E3 ligase. [Thesis]. Hong Kong University of Science and Technology; 2015. Available from: https://doi.org/10.14711/thesis-b1514880 ; http://repository.ust.hk/ir/bitstream/1783.1-80226/1/th_redirect.html

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


University of Hong Kong

27. 郭樱樱; Guo, Yingying. A study of protein phosphorylation and ubiquitination in DNA double strand break responses.

Degree: PhD, 2016, University of Hong Kong

Through altering the properties of DNA damage response (DDR) proteins, posttranslational modifications (PTMs) play pivotal roles in orchestrating timely and accurate cellular responses to DNA… (more)

Subjects/Keywords: DNA damage; Protein kinases; Ubiquitin; Phosphorylation

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APA (6th Edition):

郭樱樱; Guo, Y. (2016). A study of protein phosphorylation and ubiquitination in DNA double strand break responses. (Doctoral Dissertation). University of Hong Kong. Retrieved from Guo, Y. [郭樱樱]. (2016). A study of protein phosphorylation and ubiquitination in DNA double strand break responses. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5816256. ; http://dx.doi.org/10.5353/th_b5816256 ; http://hdl.handle.net/10722/237863

Chicago Manual of Style (16th Edition):

郭樱樱; Guo, Yingying. “A study of protein phosphorylation and ubiquitination in DNA double strand break responses.” 2016. Doctoral Dissertation, University of Hong Kong. Accessed July 18, 2019. Guo, Y. [郭樱樱]. (2016). A study of protein phosphorylation and ubiquitination in DNA double strand break responses. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5816256. ; http://dx.doi.org/10.5353/th_b5816256 ; http://hdl.handle.net/10722/237863.

MLA Handbook (7th Edition):

郭樱樱; Guo, Yingying. “A study of protein phosphorylation and ubiquitination in DNA double strand break responses.” 2016. Web. 18 Jul 2019.

Vancouver:

郭樱樱; Guo Y. A study of protein phosphorylation and ubiquitination in DNA double strand break responses. [Internet] [Doctoral dissertation]. University of Hong Kong; 2016. [cited 2019 Jul 18]. Available from: Guo, Y. [郭樱樱]. (2016). A study of protein phosphorylation and ubiquitination in DNA double strand break responses. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5816256. ; http://dx.doi.org/10.5353/th_b5816256 ; http://hdl.handle.net/10722/237863.

Council of Science Editors:

郭樱樱; Guo Y. A study of protein phosphorylation and ubiquitination in DNA double strand break responses. [Doctoral Dissertation]. University of Hong Kong; 2016. Available from: Guo, Y. [郭樱樱]. (2016). A study of protein phosphorylation and ubiquitination in DNA double strand break responses. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5816256. ; http://dx.doi.org/10.5353/th_b5816256 ; http://hdl.handle.net/10722/237863


University of Otago

28. Curry, Jack Richard. Characterisation of the ubiquitin E3 ligase COP1 .

Degree: University of Otago

 Constitutive photomorphogenic 1 (COP1) is a ubiquitin E3 ligase that has been implicated in development of a variety cancers. The goal was to characterise the… (more)

Subjects/Keywords: protein; ubiquitin; COP1

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

APA (6th Edition):

Curry, J. R. (n.d.). Characterisation of the ubiquitin E3 ligase COP1 . (Masters Thesis). University of Otago. Retrieved from http://hdl.handle.net/10523/8170

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Chicago Manual of Style (16th Edition):

Curry, Jack Richard. “Characterisation of the ubiquitin E3 ligase COP1 .” Masters Thesis, University of Otago. Accessed July 18, 2019. http://hdl.handle.net/10523/8170.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

MLA Handbook (7th Edition):

Curry, Jack Richard. “Characterisation of the ubiquitin E3 ligase COP1 .” Web. 18 Jul 2019.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Curry JR. Characterisation of the ubiquitin E3 ligase COP1 . [Internet] [Masters thesis]. University of Otago; [cited 2019 Jul 18]. Available from: http://hdl.handle.net/10523/8170.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Council of Science Editors:

Curry JR. Characterisation of the ubiquitin E3 ligase COP1 . [Masters Thesis]. University of Otago; Available from: http://hdl.handle.net/10523/8170

Note: this citation may be lacking information needed for this citation format:
No year of publication.


University of Manchester

29. Stefani, Flavia. Characterising the function of Ubiquitin associated protein 1 (UBAP1).

Degree: 2013, University of Manchester

 Inactivating EGF signalling is key to modulating cell growth and avoidingcancer. To do this, the EGF receptor is ubiquitinated, internalized and sorted tolysosome for degradation.… (more)

Subjects/Keywords: Ubiquitin; ESCRT machinery; UBAP1; HDPTP; TSG101

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

APA (6th Edition):

Stefani, F. (2013). Characterising the function of Ubiquitin associated protein 1 (UBAP1). (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:198787

Chicago Manual of Style (16th Edition):

Stefani, Flavia. “Characterising the function of Ubiquitin associated protein 1 (UBAP1).” 2013. Doctoral Dissertation, University of Manchester. Accessed July 18, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:198787.

MLA Handbook (7th Edition):

Stefani, Flavia. “Characterising the function of Ubiquitin associated protein 1 (UBAP1).” 2013. Web. 18 Jul 2019.

Vancouver:

Stefani F. Characterising the function of Ubiquitin associated protein 1 (UBAP1). [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2019 Jul 18]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:198787.

Council of Science Editors:

Stefani F. Characterising the function of Ubiquitin associated protein 1 (UBAP1). [Doctoral Dissertation]. University of Manchester; 2013. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:198787


University of Washington

30. Whedon, Sam. Chemical strategies for investigation of deubiquitinases.

Degree: PhD, 2019, University of Washington

 Regulation of protein structure and function by post-translational modification is a key mechanism in cellular homeostasis. Among known modifications the small protein ubiquitin is unique… (more)

Subjects/Keywords: dehydroalanine; deubiquitinase; selenocysteine; ubiquitin; Organic chemistry; Chemistry

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

APA (6th Edition):

Whedon, S. (2019). Chemical strategies for investigation of deubiquitinases. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/43327

Chicago Manual of Style (16th Edition):

Whedon, Sam. “Chemical strategies for investigation of deubiquitinases.” 2019. Doctoral Dissertation, University of Washington. Accessed July 18, 2019. http://hdl.handle.net/1773/43327.

MLA Handbook (7th Edition):

Whedon, Sam. “Chemical strategies for investigation of deubiquitinases.” 2019. Web. 18 Jul 2019.

Vancouver:

Whedon S. Chemical strategies for investigation of deubiquitinases. [Internet] [Doctoral dissertation]. University of Washington; 2019. [cited 2019 Jul 18]. Available from: http://hdl.handle.net/1773/43327.

Council of Science Editors:

Whedon S. Chemical strategies for investigation of deubiquitinases. [Doctoral Dissertation]. University of Washington; 2019. Available from: http://hdl.handle.net/1773/43327

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