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You searched for subject:(protein degradation). Showing records 1 – 30 of 150 total matches.

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University of Georgia

1. Canseco, Miguel Angel. Protein nutrition of dairy cows fed high fat diets.

Degree: MS, Animal Science, 2002, University of Georgia

 Two experiments were conducted to determine the value of specific protein supplements in lactating dairy cows fed high fat diets. Experiment 1, six feedstuffs (wheat… (more)

Subjects/Keywords: Protein degradation

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

APA (6th Edition):

Canseco, M. A. (2002). Protein nutrition of dairy cows fed high fat diets. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/canseco_miguel_a_200208_ms

Chicago Manual of Style (16th Edition):

Canseco, Miguel Angel. “Protein nutrition of dairy cows fed high fat diets.” 2002. Masters Thesis, University of Georgia. Accessed August 04, 2020. http://purl.galileo.usg.edu/uga_etd/canseco_miguel_a_200208_ms.

MLA Handbook (7th Edition):

Canseco, Miguel Angel. “Protein nutrition of dairy cows fed high fat diets.” 2002. Web. 04 Aug 2020.

Vancouver:

Canseco MA. Protein nutrition of dairy cows fed high fat diets. [Internet] [Masters thesis]. University of Georgia; 2002. [cited 2020 Aug 04]. Available from: http://purl.galileo.usg.edu/uga_etd/canseco_miguel_a_200208_ms.

Council of Science Editors:

Canseco MA. Protein nutrition of dairy cows fed high fat diets. [Masters Thesis]. University of Georgia; 2002. Available from: http://purl.galileo.usg.edu/uga_etd/canseco_miguel_a_200208_ms


Deakin University

2. Brown, Erin. The role of PGC-1α and PGC-1β in myotube protein synthesis.

Degree: School of Exercise and Nutritional Sciences, 2013, Deakin University

 Skeletal muscle mass is regulated by a balance between protein synthesis and protein degradation. Using molecular techniques, this PhD thesis identified that two proteins, PGC-1α… (more)

Subjects/Keywords: Protein synthesis; Protein degradation; Skeletal muscle atrophy

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APA (6th Edition):

Brown, E. (2013). The role of PGC-1α and PGC-1β in myotube protein synthesis. (Thesis). Deakin University. Retrieved from http://hdl.handle.net/10536/DRO/DU:30063004

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):

Brown, Erin. “The role of PGC-1α and PGC-1β in myotube protein synthesis.” 2013. Thesis, Deakin University. Accessed August 04, 2020. http://hdl.handle.net/10536/DRO/DU:30063004.

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

MLA Handbook (7th Edition):

Brown, Erin. “The role of PGC-1α and PGC-1β in myotube protein synthesis.” 2013. Web. 04 Aug 2020.

Vancouver:

Brown E. The role of PGC-1α and PGC-1β in myotube protein synthesis. [Internet] [Thesis]. Deakin University; 2013. [cited 2020 Aug 04]. Available from: http://hdl.handle.net/10536/DRO/DU:30063004.

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

Council of Science Editors:

Brown E. The role of PGC-1α and PGC-1β in myotube protein synthesis. [Thesis]. Deakin University; 2013. Available from: http://hdl.handle.net/10536/DRO/DU:30063004

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


Rice University

3. Liu, Yiwen. Optimization of Proteasomal Degradation Reporter (eDeg-On) System for CRISPR-mediated Whole-genome Knockout Screens.

Degree: MA, Natural Sciences, 2017, Rice University

Protein folding and clearance of misfolded proteins are crucial to maintain cellular homeostasis (Jariel-Encontre et al., 2008). Misfolded proteins may associate with other cellular components… (more)

Subjects/Keywords: UPS; CRISPR-cas; eDeg-On; protein degradation

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APA (6th Edition):

Liu, Y. (2017). Optimization of Proteasomal Degradation Reporter (eDeg-On) System for CRISPR-mediated Whole-genome Knockout Screens. (Masters Thesis). Rice University. Retrieved from http://hdl.handle.net/1911/96138

Chicago Manual of Style (16th Edition):

Liu, Yiwen. “Optimization of Proteasomal Degradation Reporter (eDeg-On) System for CRISPR-mediated Whole-genome Knockout Screens.” 2017. Masters Thesis, Rice University. Accessed August 04, 2020. http://hdl.handle.net/1911/96138.

MLA Handbook (7th Edition):

Liu, Yiwen. “Optimization of Proteasomal Degradation Reporter (eDeg-On) System for CRISPR-mediated Whole-genome Knockout Screens.” 2017. Web. 04 Aug 2020.

Vancouver:

Liu Y. Optimization of Proteasomal Degradation Reporter (eDeg-On) System for CRISPR-mediated Whole-genome Knockout Screens. [Internet] [Masters thesis]. Rice University; 2017. [cited 2020 Aug 04]. Available from: http://hdl.handle.net/1911/96138.

Council of Science Editors:

Liu Y. Optimization of Proteasomal Degradation Reporter (eDeg-On) System for CRISPR-mediated Whole-genome Knockout Screens. [Masters Thesis]. Rice University; 2017. Available from: http://hdl.handle.net/1911/96138


University of Toronto

4. Esmail, Sally. Elucidating the Molecular Mechanisms Involved in Assembly/Folding and Targeting V-ATPase a-subunit Isoforms to their Functional Destinations.

Degree: PhD, 2017, University of Toronto

 Vacuolar H+-ATPases (V-ATPases) are proton pumps distributed across membranes of specialized cells and luminal compartments. V-ATPases in the plasma membrane of osteoclasts are responsible for… (more)

Subjects/Keywords: ER-associated degradation; Membrane protein; N-glycosylation; Protein degradation; Trafficking; V-ATPases; 0487

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APA (6th Edition):

Esmail, S. (2017). Elucidating the Molecular Mechanisms Involved in Assembly/Folding and Targeting V-ATPase a-subunit Isoforms to their Functional Destinations. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/80727

Chicago Manual of Style (16th Edition):

Esmail, Sally. “Elucidating the Molecular Mechanisms Involved in Assembly/Folding and Targeting V-ATPase a-subunit Isoforms to their Functional Destinations.” 2017. Doctoral Dissertation, University of Toronto. Accessed August 04, 2020. http://hdl.handle.net/1807/80727.

MLA Handbook (7th Edition):

Esmail, Sally. “Elucidating the Molecular Mechanisms Involved in Assembly/Folding and Targeting V-ATPase a-subunit Isoforms to their Functional Destinations.” 2017. Web. 04 Aug 2020.

Vancouver:

Esmail S. Elucidating the Molecular Mechanisms Involved in Assembly/Folding and Targeting V-ATPase a-subunit Isoforms to their Functional Destinations. [Internet] [Doctoral dissertation]. University of Toronto; 2017. [cited 2020 Aug 04]. Available from: http://hdl.handle.net/1807/80727.

Council of Science Editors:

Esmail S. Elucidating the Molecular Mechanisms Involved in Assembly/Folding and Targeting V-ATPase a-subunit Isoforms to their Functional Destinations. [Doctoral Dissertation]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/80727


UCLA

5. Lau, Edward. Mitochondrial Protein Dynamics in Cardiac Remodeling.

Degree: Molec, Cell, & Integ Physiology, 2014, UCLA

 The cardiac mitochondrial proteome contains ~1,500 distinct proteins that carry out necessary metabolic and energetic processes in the heart. To sustain cardiac function, the mitochondrial… (more)

Subjects/Keywords: Physiology; Cardiac hypertrophy; Heavy water; Mitochondria; Protein degradation; Protein turnover; Proteomics

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APA (6th Edition):

Lau, E. (2014). Mitochondrial Protein Dynamics in Cardiac Remodeling. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/3sj7b8gc

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):

Lau, Edward. “Mitochondrial Protein Dynamics in Cardiac Remodeling.” 2014. Thesis, UCLA. Accessed August 04, 2020. http://www.escholarship.org/uc/item/3sj7b8gc.

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

MLA Handbook (7th Edition):

Lau, Edward. “Mitochondrial Protein Dynamics in Cardiac Remodeling.” 2014. Web. 04 Aug 2020.

Vancouver:

Lau E. Mitochondrial Protein Dynamics in Cardiac Remodeling. [Internet] [Thesis]. UCLA; 2014. [cited 2020 Aug 04]. Available from: http://www.escholarship.org/uc/item/3sj7b8gc.

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

Council of Science Editors:

Lau E. Mitochondrial Protein Dynamics in Cardiac Remodeling. [Thesis]. UCLA; 2014. Available from: http://www.escholarship.org/uc/item/3sj7b8gc

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


West Virginia University

6. Thibaudeau, Tiffany Ann. Elucidating a Common Mechanism of Proteasome Impairment in Neurodegenerative Disease and its Pharmacological Intervention.

Degree: PhD, Biochemistry, 2019, West Virginia University

  Proteostasis is maintained by several systems in the cell including the ubiquitin-proteasome system (UPS), chaperones, chaperone-mediated autophagy, and macroautophagy. The UPS is the principle… (more)

Subjects/Keywords: proteasome; protein degradation; proteasome gate; neurodegeneration; protein oligomers; Biochemistry

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APA (6th Edition):

Thibaudeau, T. A. (2019). Elucidating a Common Mechanism of Proteasome Impairment in Neurodegenerative Disease and its Pharmacological Intervention. (Doctoral Dissertation). West Virginia University. Retrieved from https://doi.org/10.33915/etd.3780 ; https://researchrepository.wvu.edu/etd/3780

Chicago Manual of Style (16th Edition):

Thibaudeau, Tiffany Ann. “Elucidating a Common Mechanism of Proteasome Impairment in Neurodegenerative Disease and its Pharmacological Intervention.” 2019. Doctoral Dissertation, West Virginia University. Accessed August 04, 2020. https://doi.org/10.33915/etd.3780 ; https://researchrepository.wvu.edu/etd/3780.

MLA Handbook (7th Edition):

Thibaudeau, Tiffany Ann. “Elucidating a Common Mechanism of Proteasome Impairment in Neurodegenerative Disease and its Pharmacological Intervention.” 2019. Web. 04 Aug 2020.

Vancouver:

Thibaudeau TA. Elucidating a Common Mechanism of Proteasome Impairment in Neurodegenerative Disease and its Pharmacological Intervention. [Internet] [Doctoral dissertation]. West Virginia University; 2019. [cited 2020 Aug 04]. Available from: https://doi.org/10.33915/etd.3780 ; https://researchrepository.wvu.edu/etd/3780.

Council of Science Editors:

Thibaudeau TA. Elucidating a Common Mechanism of Proteasome Impairment in Neurodegenerative Disease and its Pharmacological Intervention. [Doctoral Dissertation]. West Virginia University; 2019. Available from: https://doi.org/10.33915/etd.3780 ; https://researchrepository.wvu.edu/etd/3780


Virginia Tech

7. Seymour, Kacie Tinnesz. Examining the Influence of Muscle Fiber Type on Protein Turnover Signaling in Growing Pigs.

Degree: MS, Animal and Poultry Sciences, 2020, Virginia Tech

 Skeletal muscles grow by increasing the amount of protein contained within them. The amount of protein deposited is determined by the net balance between the… (more)

Subjects/Keywords: pig; muscle fiber type; skeletal muscle; protein synthesis; protein degradation

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APA (6th Edition):

Seymour, K. T. (2020). Examining the Influence of Muscle Fiber Type on Protein Turnover Signaling in Growing Pigs. (Masters Thesis). Virginia Tech. Retrieved from http://hdl.handle.net/10919/98592

Chicago Manual of Style (16th Edition):

Seymour, Kacie Tinnesz. “Examining the Influence of Muscle Fiber Type on Protein Turnover Signaling in Growing Pigs.” 2020. Masters Thesis, Virginia Tech. Accessed August 04, 2020. http://hdl.handle.net/10919/98592.

MLA Handbook (7th Edition):

Seymour, Kacie Tinnesz. “Examining the Influence of Muscle Fiber Type on Protein Turnover Signaling in Growing Pigs.” 2020. Web. 04 Aug 2020.

Vancouver:

Seymour KT. Examining the Influence of Muscle Fiber Type on Protein Turnover Signaling in Growing Pigs. [Internet] [Masters thesis]. Virginia Tech; 2020. [cited 2020 Aug 04]. Available from: http://hdl.handle.net/10919/98592.

Council of Science Editors:

Seymour KT. Examining the Influence of Muscle Fiber Type on Protein Turnover Signaling in Growing Pigs. [Masters Thesis]. Virginia Tech; 2020. Available from: http://hdl.handle.net/10919/98592


University of Kentucky

8. Zhang, Xinyi. PROTEIN ENGINEERING IN THE STUDY OF PROTEIN LABELING AND DEGRADATION.

Degree: 2018, University of Kentucky

 Proteins are large macromolecules that play important roles in nature. With the development of modern molecular biology techniques, protein engineering has emerged as a useful… (more)

Subjects/Keywords: protein engineering; protein tag; immobilization; degradation; Biochemistry; Molecular Biology; Structural Biology

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APA (6th Edition):

Zhang, X. (2018). PROTEIN ENGINEERING IN THE STUDY OF PROTEIN LABELING AND DEGRADATION. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/chemistry_etds/93

Chicago Manual of Style (16th Edition):

Zhang, Xinyi. “PROTEIN ENGINEERING IN THE STUDY OF PROTEIN LABELING AND DEGRADATION.” 2018. Doctoral Dissertation, University of Kentucky. Accessed August 04, 2020. https://uknowledge.uky.edu/chemistry_etds/93.

MLA Handbook (7th Edition):

Zhang, Xinyi. “PROTEIN ENGINEERING IN THE STUDY OF PROTEIN LABELING AND DEGRADATION.” 2018. Web. 04 Aug 2020.

Vancouver:

Zhang X. PROTEIN ENGINEERING IN THE STUDY OF PROTEIN LABELING AND DEGRADATION. [Internet] [Doctoral dissertation]. University of Kentucky; 2018. [cited 2020 Aug 04]. Available from: https://uknowledge.uky.edu/chemistry_etds/93.

Council of Science Editors:

Zhang X. PROTEIN ENGINEERING IN THE STUDY OF PROTEIN LABELING AND DEGRADATION. [Doctoral Dissertation]. University of Kentucky; 2018. Available from: https://uknowledge.uky.edu/chemistry_etds/93


Rice University

9. Zhao, Wenting. From detection of proteasomal degradation to targeted control of protein depletion.

Degree: PhD, Engineering, 2017, Rice University

 The ubiquitin proteasome system (UPS) regulates protein turnover and catalyzes degradation of misfolded or damaged proteins, thus playing an important role in maintaining protein homoeostasis… (more)

Subjects/Keywords: Ubiquitin-Proteasome System; Protein Degradation; Control protein level; Synthetic Biology

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APA (6th Edition):

Zhao, W. (2017). From detection of proteasomal degradation to targeted control of protein depletion. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/105502

Chicago Manual of Style (16th Edition):

Zhao, Wenting. “From detection of proteasomal degradation to targeted control of protein depletion.” 2017. Doctoral Dissertation, Rice University. Accessed August 04, 2020. http://hdl.handle.net/1911/105502.

MLA Handbook (7th Edition):

Zhao, Wenting. “From detection of proteasomal degradation to targeted control of protein depletion.” 2017. Web. 04 Aug 2020.

Vancouver:

Zhao W. From detection of proteasomal degradation to targeted control of protein depletion. [Internet] [Doctoral dissertation]. Rice University; 2017. [cited 2020 Aug 04]. Available from: http://hdl.handle.net/1911/105502.

Council of Science Editors:

Zhao W. From detection of proteasomal degradation to targeted control of protein depletion. [Doctoral Dissertation]. Rice University; 2017. Available from: http://hdl.handle.net/1911/105502


University of Cincinnati

10. Tonddast-Navaei, Sam, M.S. Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines.

Degree: PhD, Arts and Sciences: Chemistry, 2014, University of Cincinnati

 Proteins are large complex molecules that play important roles in cellular activities such as DNA replication, molecular transport, cell immunity, and regulatory activities. Based on… (more)

Subjects/Keywords: Physical Chemistry; Protein unfolding; Protein translocation; Protein degradation; ATPase; p97; Molecular Dynamics

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APA (6th Edition):

Tonddast-Navaei, Sam, M. S. (2014). Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384869946

Chicago Manual of Style (16th Edition):

Tonddast-Navaei, Sam, M S. “Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines.” 2014. Doctoral Dissertation, University of Cincinnati. Accessed August 04, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384869946.

MLA Handbook (7th Edition):

Tonddast-Navaei, Sam, M S. “Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines.” 2014. Web. 04 Aug 2020.

Vancouver:

Tonddast-Navaei, Sam MS. Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines. [Internet] [Doctoral dissertation]. University of Cincinnati; 2014. [cited 2020 Aug 04]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384869946.

Council of Science Editors:

Tonddast-Navaei, Sam MS. Mechanism of Substrate Protein Remodeling by Allosteric Motions of AAA+ Nanomachines. [Doctoral Dissertation]. University of Cincinnati; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384869946


University of Toronto

11. Tsai, Allen Yi-Lun. Post-translational Regulations of FUSCA3 in Arabidopsis thaliana.

Degree: 2013, University of Toronto

Seed formation consists of two major stages: embryo pattern formation and maturation. During seed maturation, the embryo accumulates storage material, acquires desiccation tolerance, and enters… (more)

Subjects/Keywords: Development; Protein-protein interaction; Phosphorylation; Phase transition; Plant hormone; Protein degradation; 0309

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APA (6th Edition):

Tsai, A. Y. (2013). Post-translational Regulations of FUSCA3 in Arabidopsis thaliana. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/36018

Chicago Manual of Style (16th Edition):

Tsai, Allen Yi-Lun. “Post-translational Regulations of FUSCA3 in Arabidopsis thaliana.” 2013. Doctoral Dissertation, University of Toronto. Accessed August 04, 2020. http://hdl.handle.net/1807/36018.

MLA Handbook (7th Edition):

Tsai, Allen Yi-Lun. “Post-translational Regulations of FUSCA3 in Arabidopsis thaliana.” 2013. Web. 04 Aug 2020.

Vancouver:

Tsai AY. Post-translational Regulations of FUSCA3 in Arabidopsis thaliana. [Internet] [Doctoral dissertation]. University of Toronto; 2013. [cited 2020 Aug 04]. Available from: http://hdl.handle.net/1807/36018.

Council of Science Editors:

Tsai AY. Post-translational Regulations of FUSCA3 in Arabidopsis thaliana. [Doctoral Dissertation]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/36018


Freie Universität Berlin

12. Seeger, Michael. Funktionelle Aspekte des Ubiquitin-Proteasom-Systems.

Degree: 2015, Freie Universität Berlin

 Die Synthese und Reifung von Proteinen des endoplasmatischen Retikulums (ER) wird durch ein komplexes Qualitätskontrollsystem überwacht. So werden bei der Akkumulation fehlerhafter Proteine im ER… (more)

Subjects/Keywords: protein degradation; ubiquitin; proteasome; endoplasmic reticulum; ER-associated protein degradation; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Seeger, M. (2015). Funktionelle Aspekte des Ubiquitin-Proteasom-Systems. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-12453

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):

Seeger, Michael. “Funktionelle Aspekte des Ubiquitin-Proteasom-Systems.” 2015. Thesis, Freie Universität Berlin. Accessed August 04, 2020. http://dx.doi.org/10.17169/refubium-12453.

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

MLA Handbook (7th Edition):

Seeger, Michael. “Funktionelle Aspekte des Ubiquitin-Proteasom-Systems.” 2015. Web. 04 Aug 2020.

Vancouver:

Seeger M. Funktionelle Aspekte des Ubiquitin-Proteasom-Systems. [Internet] [Thesis]. Freie Universität Berlin; 2015. [cited 2020 Aug 04]. Available from: http://dx.doi.org/10.17169/refubium-12453.

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

Council of Science Editors:

Seeger M. Funktionelle Aspekte des Ubiquitin-Proteasom-Systems. [Thesis]. Freie Universität Berlin; 2015. Available from: http://dx.doi.org/10.17169/refubium-12453

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

13. Chen, Ying. Regulation of protein metabolism in skeletal muscle of low-birth-weight neonatal pigs.

Degree: PhD, Animal and Poultry Sciences, 2017, Virginia Tech

 The neonatal period in mammals is characterized by high rates of growth, attributed to rapid myonuclear accretion and protein deposition in muscle. Low-birth-weight (LBWT) neonates… (more)

Subjects/Keywords: low-birth-weight; pig; skeletal muscle; satellite cells; protein synthesis; protein degradation

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

APA (6th Edition):

Chen, Y. (2017). Regulation of protein metabolism in skeletal muscle of low-birth-weight neonatal pigs. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/88511

Chicago Manual of Style (16th Edition):

Chen, Ying. “Regulation of protein metabolism in skeletal muscle of low-birth-weight neonatal pigs.” 2017. Doctoral Dissertation, Virginia Tech. Accessed August 04, 2020. http://hdl.handle.net/10919/88511.

MLA Handbook (7th Edition):

Chen, Ying. “Regulation of protein metabolism in skeletal muscle of low-birth-weight neonatal pigs.” 2017. Web. 04 Aug 2020.

Vancouver:

Chen Y. Regulation of protein metabolism in skeletal muscle of low-birth-weight neonatal pigs. [Internet] [Doctoral dissertation]. Virginia Tech; 2017. [cited 2020 Aug 04]. Available from: http://hdl.handle.net/10919/88511.

Council of Science Editors:

Chen Y. Regulation of protein metabolism in skeletal muscle of low-birth-weight neonatal pigs. [Doctoral Dissertation]. Virginia Tech; 2017. Available from: http://hdl.handle.net/10919/88511


University of California – San Francisco

14. Smith, Melanie Hennebry. The Recognition, Regulation and Roles of Misfolded Proteins in the Cell.

Degree: Biophysics, 2014, University of California – San Francisco

 The three dimensional structure of a protein, or its native state, determines its function. Yet, the process of folding into the native state is not… (more)

Subjects/Keywords: Biophysics; Biochemistry; endoplasmic reticulum; endoplasmic reticulum associated degradation; prion; Protein folding; unfolded protein response

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APA (6th Edition):

Smith, M. H. (2014). The Recognition, Regulation and Roles of Misfolded Proteins in the Cell. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/8rf373zp

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):

Smith, Melanie Hennebry. “The Recognition, Regulation and Roles of Misfolded Proteins in the Cell.” 2014. Thesis, University of California – San Francisco. Accessed August 04, 2020. http://www.escholarship.org/uc/item/8rf373zp.

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

MLA Handbook (7th Edition):

Smith, Melanie Hennebry. “The Recognition, Regulation and Roles of Misfolded Proteins in the Cell.” 2014. Web. 04 Aug 2020.

Vancouver:

Smith MH. The Recognition, Regulation and Roles of Misfolded Proteins in the Cell. [Internet] [Thesis]. University of California – San Francisco; 2014. [cited 2020 Aug 04]. Available from: http://www.escholarship.org/uc/item/8rf373zp.

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

Council of Science Editors:

Smith MH. The Recognition, Regulation and Roles of Misfolded Proteins in the Cell. [Thesis]. University of California – San Francisco; 2014. Available from: http://www.escholarship.org/uc/item/8rf373zp

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


University of Alberta

15. Armstrong, Stephen, R. Role of the E-3 ligase CHIP in the negative regulation of the transcription factor TAp63.

Degree: PhD, Medical Sciences-Laboratory Medicine and Pathology, 2016, University of Alberta

 The p53 family of tumor suppressors is an important group of transcription factors preventing the development of cancer by targeting cell-cycle arrest and apoptosis mediator… (more)

Subjects/Keywords: p63; TAp63; CHIP; ubiquitination; tumor suppressor; protein degradation

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APA (6th Edition):

Armstrong, Stephen, R. (2016). Role of the E-3 ligase CHIP in the negative regulation of the transcription factor TAp63. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/cgx41mj158

Chicago Manual of Style (16th Edition):

Armstrong, Stephen, R. “Role of the E-3 ligase CHIP in the negative regulation of the transcription factor TAp63.” 2016. Doctoral Dissertation, University of Alberta. Accessed August 04, 2020. https://era.library.ualberta.ca/files/cgx41mj158.

MLA Handbook (7th Edition):

Armstrong, Stephen, R. “Role of the E-3 ligase CHIP in the negative regulation of the transcription factor TAp63.” 2016. Web. 04 Aug 2020.

Vancouver:

Armstrong, Stephen R. Role of the E-3 ligase CHIP in the negative regulation of the transcription factor TAp63. [Internet] [Doctoral dissertation]. University of Alberta; 2016. [cited 2020 Aug 04]. Available from: https://era.library.ualberta.ca/files/cgx41mj158.

Council of Science Editors:

Armstrong, Stephen R. Role of the E-3 ligase CHIP in the negative regulation of the transcription factor TAp63. [Doctoral Dissertation]. University of Alberta; 2016. Available from: https://era.library.ualberta.ca/files/cgx41mj158


University of Louisville

16. Zong, Chenggong. Explore the murine cardiac 20S proteasomes : molecular composition and regulation.

Degree: PhD, 2005, University of Louisville

 20S proteasome, essential component of protein degradation mechanism, is important to maintain homeostasis. Its malfunctions have been associated with several pathological conditions. This study presents… (more)

Subjects/Keywords: Cardiac; Proteasomes; Protein degradation; Phosphorylation

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APA (6th Edition):

Zong, C. (2005). Explore the murine cardiac 20S proteasomes : molecular composition and regulation. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/1654 ; https://ir.library.louisville.edu/etd/1654

Chicago Manual of Style (16th Edition):

Zong, Chenggong. “Explore the murine cardiac 20S proteasomes : molecular composition and regulation.” 2005. Doctoral Dissertation, University of Louisville. Accessed August 04, 2020. 10.18297/etd/1654 ; https://ir.library.louisville.edu/etd/1654.

MLA Handbook (7th Edition):

Zong, Chenggong. “Explore the murine cardiac 20S proteasomes : molecular composition and regulation.” 2005. Web. 04 Aug 2020.

Vancouver:

Zong C. Explore the murine cardiac 20S proteasomes : molecular composition and regulation. [Internet] [Doctoral dissertation]. University of Louisville; 2005. [cited 2020 Aug 04]. Available from: 10.18297/etd/1654 ; https://ir.library.louisville.edu/etd/1654.

Council of Science Editors:

Zong C. Explore the murine cardiac 20S proteasomes : molecular composition and regulation. [Doctoral Dissertation]. University of Louisville; 2005. Available from: 10.18297/etd/1654 ; https://ir.library.louisville.edu/etd/1654


Universiteit Utrecht

17. Ruijtenberg, S.A. PROTEIN DEGRADATION BY THE ANAPHASE PROMOTING COMPLEX IN SPACE AND TIME -A role for the intrinsic characteristics of the substrates-.

Degree: 2009, Universiteit Utrecht

 In order to create two new daughter cells out of one mother cell, a cell has to duplicate genetic information through DNA replication during S-phase… (more)

Subjects/Keywords: Geneeskunde; APC/C; protein degradation; temporal order; substrates

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APA (6th Edition):

Ruijtenberg, S. A. (2009). PROTEIN DEGRADATION BY THE ANAPHASE PROMOTING COMPLEX IN SPACE AND TIME -A role for the intrinsic characteristics of the substrates-. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/37183

Chicago Manual of Style (16th Edition):

Ruijtenberg, S A. “PROTEIN DEGRADATION BY THE ANAPHASE PROMOTING COMPLEX IN SPACE AND TIME -A role for the intrinsic characteristics of the substrates-.” 2009. Masters Thesis, Universiteit Utrecht. Accessed August 04, 2020. http://dspace.library.uu.nl:8080/handle/1874/37183.

MLA Handbook (7th Edition):

Ruijtenberg, S A. “PROTEIN DEGRADATION BY THE ANAPHASE PROMOTING COMPLEX IN SPACE AND TIME -A role for the intrinsic characteristics of the substrates-.” 2009. Web. 04 Aug 2020.

Vancouver:

Ruijtenberg SA. PROTEIN DEGRADATION BY THE ANAPHASE PROMOTING COMPLEX IN SPACE AND TIME -A role for the intrinsic characteristics of the substrates-. [Internet] [Masters thesis]. Universiteit Utrecht; 2009. [cited 2020 Aug 04]. Available from: http://dspace.library.uu.nl:8080/handle/1874/37183.

Council of Science Editors:

Ruijtenberg SA. PROTEIN DEGRADATION BY THE ANAPHASE PROMOTING COMPLEX IN SPACE AND TIME -A role for the intrinsic characteristics of the substrates-. [Masters Thesis]. Universiteit Utrecht; 2009. Available from: http://dspace.library.uu.nl:8080/handle/1874/37183

18. M.E. Pozzebon. A BC-BOX DOMAIN-RELATED MECHANISM FOR VHL PROTEIN DEGRADATION.

Degree: 2011, Università degli Studi di Milano

 Viruses need to hijack cellular machineries both for their replication and propagation and to overcome cellular defenses. Since they often reconvert the functions of host… (more)

Subjects/Keywords: VHL; protein degradation; virus; BC-box domain; Settore BIO/10 - Biochimica

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APA (6th Edition):

Pozzebon, M. (2011). A BC-BOX DOMAIN-RELATED MECHANISM FOR VHL PROTEIN DEGRADATION. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/157938

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):

Pozzebon, M.E.. “A BC-BOX DOMAIN-RELATED MECHANISM FOR VHL PROTEIN DEGRADATION.” 2011. Thesis, Università degli Studi di Milano. Accessed August 04, 2020. http://hdl.handle.net/2434/157938.

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

MLA Handbook (7th Edition):

Pozzebon, M.E.. “A BC-BOX DOMAIN-RELATED MECHANISM FOR VHL PROTEIN DEGRADATION.” 2011. Web. 04 Aug 2020.

Vancouver:

Pozzebon M. A BC-BOX DOMAIN-RELATED MECHANISM FOR VHL PROTEIN DEGRADATION. [Internet] [Thesis]. Università degli Studi di Milano; 2011. [cited 2020 Aug 04]. Available from: http://hdl.handle.net/2434/157938.

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

Council of Science Editors:

Pozzebon M. A BC-BOX DOMAIN-RELATED MECHANISM FOR VHL PROTEIN DEGRADATION. [Thesis]. Università degli Studi di Milano; 2011. Available from: http://hdl.handle.net/2434/157938

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


Vanderbilt University

19. Chen, Tony Wayne. Novel Biochemical Regulatory Mechanisms of Developmental Signaling Pathways.

Degree: PhD, Cell and Developmental Biology, 2014, Vanderbilt University

 The Notch signaling pathway is an essential cell-cell signaling pathway that is involved in cell fate decisions and cell differentiation during early metazoan development. In… (more)

Subjects/Keywords: Notch; protein degradation; signal transduction; Xenopus egg extract; development; cancer

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APA (6th Edition):

Chen, T. W. (2014). Novel Biochemical Regulatory Mechanisms of Developmental Signaling Pathways. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-12182014-151033/ ;

Chicago Manual of Style (16th Edition):

Chen, Tony Wayne. “Novel Biochemical Regulatory Mechanisms of Developmental Signaling Pathways.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed August 04, 2020. http://etd.library.vanderbilt.edu/available/etd-12182014-151033/ ;.

MLA Handbook (7th Edition):

Chen, Tony Wayne. “Novel Biochemical Regulatory Mechanisms of Developmental Signaling Pathways.” 2014. Web. 04 Aug 2020.

Vancouver:

Chen TW. Novel Biochemical Regulatory Mechanisms of Developmental Signaling Pathways. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2020 Aug 04]. Available from: http://etd.library.vanderbilt.edu/available/etd-12182014-151033/ ;.

Council of Science Editors:

Chen TW. Novel Biochemical Regulatory Mechanisms of Developmental Signaling Pathways. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://etd.library.vanderbilt.edu/available/etd-12182014-151033/ ;

20. Persson, Frida. Investigating cell wall degradation treatments, pH-shifting and extrusion as methods to increase the quality of Paecilomyces variotii as a protein source in fish feed .

Degree: Chalmers tekniska högskola / Institutionen för biologi och bioteknik, 2019, Chalmers University of Technology

 The increased demand for seafood, due to both population growth and an increased health awareness, has resulted in an increased demand for fish feed in… (more)

Subjects/Keywords: single cell protein; cell wall degradation; fish feed; filamentous fungi

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APA (6th Edition):

Persson, F. (2019). Investigating cell wall degradation treatments, pH-shifting and extrusion as methods to increase the quality of Paecilomyces variotii as a protein source in fish feed . (Thesis). Chalmers University of Technology. Retrieved from http://hdl.handle.net/20.500.12380/300739

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):

Persson, Frida. “Investigating cell wall degradation treatments, pH-shifting and extrusion as methods to increase the quality of Paecilomyces variotii as a protein source in fish feed .” 2019. Thesis, Chalmers University of Technology. Accessed August 04, 2020. http://hdl.handle.net/20.500.12380/300739.

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

MLA Handbook (7th Edition):

Persson, Frida. “Investigating cell wall degradation treatments, pH-shifting and extrusion as methods to increase the quality of Paecilomyces variotii as a protein source in fish feed .” 2019. Web. 04 Aug 2020.

Vancouver:

Persson F. Investigating cell wall degradation treatments, pH-shifting and extrusion as methods to increase the quality of Paecilomyces variotii as a protein source in fish feed . [Internet] [Thesis]. Chalmers University of Technology; 2019. [cited 2020 Aug 04]. Available from: http://hdl.handle.net/20.500.12380/300739.

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

Council of Science Editors:

Persson F. Investigating cell wall degradation treatments, pH-shifting and extrusion as methods to increase the quality of Paecilomyces variotii as a protein source in fish feed . [Thesis]. Chalmers University of Technology; 2019. Available from: http://hdl.handle.net/20.500.12380/300739

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


University of Cambridge

21. Kisonaite, Migle. Substrate recognition by the 26S proteasome.

Degree: PhD, 2020, University of Cambridge

 The 26S proteasome is a large protein complex found in all eukaryotes. It controls the degradation of a wide range of proteins in the cell,… (more)

Subjects/Keywords: 26S proteasome; cryo-electron microscopy; protein degradation; degron; proteolysis

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APA (6th Edition):

Kisonaite, M. (2020). Substrate recognition by the 26S proteasome. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/293474

Chicago Manual of Style (16th Edition):

Kisonaite, Migle. “Substrate recognition by the 26S proteasome.” 2020. Doctoral Dissertation, University of Cambridge. Accessed August 04, 2020. https://www.repository.cam.ac.uk/handle/1810/293474.

MLA Handbook (7th Edition):

Kisonaite, Migle. “Substrate recognition by the 26S proteasome.” 2020. Web. 04 Aug 2020.

Vancouver:

Kisonaite M. Substrate recognition by the 26S proteasome. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2020 Aug 04]. Available from: https://www.repository.cam.ac.uk/handle/1810/293474.

Council of Science Editors:

Kisonaite M. Substrate recognition by the 26S proteasome. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/293474

22. Gardner, Robert Christopher. Peptidyl boronic acid inhibitors of proteasomes.

Degree: PhD, 2000, University of Bristol

Subjects/Keywords: 572; Enzyme inhibitor; Protein degradation

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APA (6th Edition):

Gardner, R. C. (2000). Peptidyl boronic acid inhibitors of proteasomes. (Doctoral Dissertation). University of Bristol. Retrieved from http://hdl.handle.net/1983/f5a3e878-ec8a-472a-a00b-1b806c004f5e

Chicago Manual of Style (16th Edition):

Gardner, Robert Christopher. “Peptidyl boronic acid inhibitors of proteasomes.” 2000. Doctoral Dissertation, University of Bristol. Accessed August 04, 2020. http://hdl.handle.net/1983/f5a3e878-ec8a-472a-a00b-1b806c004f5e.

MLA Handbook (7th Edition):

Gardner, Robert Christopher. “Peptidyl boronic acid inhibitors of proteasomes.” 2000. Web. 04 Aug 2020.

Vancouver:

Gardner RC. Peptidyl boronic acid inhibitors of proteasomes. [Internet] [Doctoral dissertation]. University of Bristol; 2000. [cited 2020 Aug 04]. Available from: http://hdl.handle.net/1983/f5a3e878-ec8a-472a-a00b-1b806c004f5e.

Council of Science Editors:

Gardner RC. Peptidyl boronic acid inhibitors of proteasomes. [Doctoral Dissertation]. University of Bristol; 2000. Available from: http://hdl.handle.net/1983/f5a3e878-ec8a-472a-a00b-1b806c004f5e


San Jose State University

23. Farshbaf, Mozhgan. Mastermind is Ubiquitinated and Degraded: Functional Consequence for Notch Signaling.

Degree: MS, Biological Sciences, 2011, San Jose State University

  Notch signaling plays a crucial role in cell development and proliferation. The Notch receptor is an inducible transcription factor found on the cell surface.… (more)

Subjects/Keywords: MAML1; Mastermind-Like Protein Family; Notch Signaling; Proteasomal degradation; Uniquitination

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APA (6th Edition):

Farshbaf, M. (2011). Mastermind is Ubiquitinated and Degraded: Functional Consequence for Notch Signaling. (Masters Thesis). San Jose State University. Retrieved from https://doi.org/10.31979/etd.mkt9-mpus ; https://scholarworks.sjsu.edu/etd_theses/4045

Chicago Manual of Style (16th Edition):

Farshbaf, Mozhgan. “Mastermind is Ubiquitinated and Degraded: Functional Consequence for Notch Signaling.” 2011. Masters Thesis, San Jose State University. Accessed August 04, 2020. https://doi.org/10.31979/etd.mkt9-mpus ; https://scholarworks.sjsu.edu/etd_theses/4045.

MLA Handbook (7th Edition):

Farshbaf, Mozhgan. “Mastermind is Ubiquitinated and Degraded: Functional Consequence for Notch Signaling.” 2011. Web. 04 Aug 2020.

Vancouver:

Farshbaf M. Mastermind is Ubiquitinated and Degraded: Functional Consequence for Notch Signaling. [Internet] [Masters thesis]. San Jose State University; 2011. [cited 2020 Aug 04]. Available from: https://doi.org/10.31979/etd.mkt9-mpus ; https://scholarworks.sjsu.edu/etd_theses/4045.

Council of Science Editors:

Farshbaf M. Mastermind is Ubiquitinated and Degraded: Functional Consequence for Notch Signaling. [Masters Thesis]. San Jose State University; 2011. Available from: https://doi.org/10.31979/etd.mkt9-mpus ; https://scholarworks.sjsu.edu/etd_theses/4045


East Carolina University

24. Davis, Patrick R. AMP Deaminase 3 in Skeletal Muscle Atrophy: Regulation of Protein Degradation and Contractile Performance.

Degree: PhD, PHD-Bioenergetics and Exer Sci, 2015, East Carolina University

 Skeletal muscle atrophy is characterized by depressed cellular energetics, increased rates of protein degradation, contractile deficits and loss of muscle mass. A potential regulator of… (more)

Subjects/Keywords: AMP deaminase; Protein degradation; Energetics; Muscular atrophy; Enzymes; Biological control systems

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APA (6th Edition):

Davis, P. R. (2015). AMP Deaminase 3 in Skeletal Muscle Atrophy: Regulation of Protein Degradation and Contractile Performance. (Doctoral Dissertation). East Carolina University. Retrieved from http://hdl.handle.net/10342/5118

Chicago Manual of Style (16th Edition):

Davis, Patrick R. “AMP Deaminase 3 in Skeletal Muscle Atrophy: Regulation of Protein Degradation and Contractile Performance.” 2015. Doctoral Dissertation, East Carolina University. Accessed August 04, 2020. http://hdl.handle.net/10342/5118.

MLA Handbook (7th Edition):

Davis, Patrick R. “AMP Deaminase 3 in Skeletal Muscle Atrophy: Regulation of Protein Degradation and Contractile Performance.” 2015. Web. 04 Aug 2020.

Vancouver:

Davis PR. AMP Deaminase 3 in Skeletal Muscle Atrophy: Regulation of Protein Degradation and Contractile Performance. [Internet] [Doctoral dissertation]. East Carolina University; 2015. [cited 2020 Aug 04]. Available from: http://hdl.handle.net/10342/5118.

Council of Science Editors:

Davis PR. AMP Deaminase 3 in Skeletal Muscle Atrophy: Regulation of Protein Degradation and Contractile Performance. [Doctoral Dissertation]. East Carolina University; 2015. Available from: http://hdl.handle.net/10342/5118


University of Minnesota

25. Folger, Brian Charles. Patulin degradation by yeast protein extract.

Degree: MS, Food Science, 2014, University of Minnesota

 The mycotoxin patulin, produced by a number of fungi, most prominently Penicillium expansum, has proven problematic for the apple industry due to contamination of apple… (more)

Subjects/Keywords: Degradation; Extraction; Patulin; Protein; Toxin; Yeast; Food science

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APA (6th Edition):

Folger, B. C. (2014). Patulin degradation by yeast protein extract. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/170695

Chicago Manual of Style (16th Edition):

Folger, Brian Charles. “Patulin degradation by yeast protein extract.” 2014. Masters Thesis, University of Minnesota. Accessed August 04, 2020. http://hdl.handle.net/11299/170695.

MLA Handbook (7th Edition):

Folger, Brian Charles. “Patulin degradation by yeast protein extract.” 2014. Web. 04 Aug 2020.

Vancouver:

Folger BC. Patulin degradation by yeast protein extract. [Internet] [Masters thesis]. University of Minnesota; 2014. [cited 2020 Aug 04]. Available from: http://hdl.handle.net/11299/170695.

Council of Science Editors:

Folger BC. Patulin degradation by yeast protein extract. [Masters Thesis]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/170695

26. Cascarina, Sean Micheal. Investigation of the sequence features controlling aggregation or degradation of prion-like proteins.

Degree: PhD, Biochemistry and Molecular Biology, 2017, Colorado State University

Protein aggregates result from the conversion of soluble proteins to an insoluble form. In some cases, protein aggregates are capable of catalyzing the conversion of… (more)

Subjects/Keywords: amyloid; prion-like; proteostasis; prion; aggregation; protein degradation

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APA (6th Edition):

Cascarina, S. M. (2017). Investigation of the sequence features controlling aggregation or degradation of prion-like proteins. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/183913

Chicago Manual of Style (16th Edition):

Cascarina, Sean Micheal. “Investigation of the sequence features controlling aggregation or degradation of prion-like proteins.” 2017. Doctoral Dissertation, Colorado State University. Accessed August 04, 2020. http://hdl.handle.net/10217/183913.

MLA Handbook (7th Edition):

Cascarina, Sean Micheal. “Investigation of the sequence features controlling aggregation or degradation of prion-like proteins.” 2017. Web. 04 Aug 2020.

Vancouver:

Cascarina SM. Investigation of the sequence features controlling aggregation or degradation of prion-like proteins. [Internet] [Doctoral dissertation]. Colorado State University; 2017. [cited 2020 Aug 04]. Available from: http://hdl.handle.net/10217/183913.

Council of Science Editors:

Cascarina SM. Investigation of the sequence features controlling aggregation or degradation of prion-like proteins. [Doctoral Dissertation]. Colorado State University; 2017. Available from: http://hdl.handle.net/10217/183913


University of Saskatchewan

27. Turner, Emma. The Anaphase-Promoting Complex Interacts with Histone Modification Proteins and Chromatin Assembly Factors.

Degree: 2011, University of Saskatchewan

 The Anaphase-Promoting Complex (APC) plays an important role in cell cycle progression. This evolutionarily conserved multi-subunit ubiquitin ligase is responsible for targeting proteins that hinder… (more)

Subjects/Keywords: Anaphase-promoting complex; histone modifications; genetics; protein degradation

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APA (6th Edition):

Turner, E. (2011). The Anaphase-Promoting Complex Interacts with Histone Modification Proteins and Chromatin Assembly Factors. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2011-08-78

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):

Turner, Emma. “The Anaphase-Promoting Complex Interacts with Histone Modification Proteins and Chromatin Assembly Factors.” 2011. Thesis, University of Saskatchewan. Accessed August 04, 2020. http://hdl.handle.net/10388/ETD-2011-08-78.

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

MLA Handbook (7th Edition):

Turner, Emma. “The Anaphase-Promoting Complex Interacts with Histone Modification Proteins and Chromatin Assembly Factors.” 2011. Web. 04 Aug 2020.

Vancouver:

Turner E. The Anaphase-Promoting Complex Interacts with Histone Modification Proteins and Chromatin Assembly Factors. [Internet] [Thesis]. University of Saskatchewan; 2011. [cited 2020 Aug 04]. Available from: http://hdl.handle.net/10388/ETD-2011-08-78.

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

Council of Science Editors:

Turner E. The Anaphase-Promoting Complex Interacts with Histone Modification Proteins and Chromatin Assembly Factors. [Thesis]. University of Saskatchewan; 2011. Available from: http://hdl.handle.net/10388/ETD-2011-08-78

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


Penn State University

28. Sayeed, Ayaz. SECRETORY PROTEIN FOLDING AND THE QUALITY CONTROL OF MISFOLDED GLYCOPROTEINS.

Degree: PhD, Integrative Biosciences, 2005, Penn State University

 The Endoplasmic Reticulum (ER) provides a special environment that caters to the maturation of secretory and membrane proteins. The folding of these proteins into their… (more)

Subjects/Keywords: Endoplasmic Reticulum; Protein Folding; Protein Degradation; Protein Quality Control

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APA (6th Edition):

Sayeed, A. (2005). SECRETORY PROTEIN FOLDING AND THE QUALITY CONTROL OF MISFOLDED GLYCOPROTEINS. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/6663

Chicago Manual of Style (16th Edition):

Sayeed, Ayaz. “SECRETORY PROTEIN FOLDING AND THE QUALITY CONTROL OF MISFOLDED GLYCOPROTEINS.” 2005. Doctoral Dissertation, Penn State University. Accessed August 04, 2020. https://etda.libraries.psu.edu/catalog/6663.

MLA Handbook (7th Edition):

Sayeed, Ayaz. “SECRETORY PROTEIN FOLDING AND THE QUALITY CONTROL OF MISFOLDED GLYCOPROTEINS.” 2005. Web. 04 Aug 2020.

Vancouver:

Sayeed A. SECRETORY PROTEIN FOLDING AND THE QUALITY CONTROL OF MISFOLDED GLYCOPROTEINS. [Internet] [Doctoral dissertation]. Penn State University; 2005. [cited 2020 Aug 04]. Available from: https://etda.libraries.psu.edu/catalog/6663.

Council of Science Editors:

Sayeed A. SECRETORY PROTEIN FOLDING AND THE QUALITY CONTROL OF MISFOLDED GLYCOPROTEINS. [Doctoral Dissertation]. Penn State University; 2005. Available from: https://etda.libraries.psu.edu/catalog/6663


Macquarie University

29. Moll, Jens Mark. Structural characterisation of yeast Lsm protein complexes.

Degree: PhD, 2011, Macquarie University

Bibliography: p. 179-195.

Introduction  – Materials and methods  – Solution behaviour of Lsm polyproteins  – Biophysical characterisation of Lsm complexes and their RNA interactions  –… (more)

Subjects/Keywords: RNA-protein interactions; Nucleoproteins; Recombinant proteins; Protein-protein interactions; Complex compounds; Lsm; Sm like; mRNA degradation; macromolecular complexes

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APA (6th Edition):

Moll, J. M. (2011). Structural characterisation of yeast Lsm protein complexes. (Doctoral Dissertation). Macquarie University. Retrieved from http://hdl.handle.net/1959.14/192059

Chicago Manual of Style (16th Edition):

Moll, Jens Mark. “Structural characterisation of yeast Lsm protein complexes.” 2011. Doctoral Dissertation, Macquarie University. Accessed August 04, 2020. http://hdl.handle.net/1959.14/192059.

MLA Handbook (7th Edition):

Moll, Jens Mark. “Structural characterisation of yeast Lsm protein complexes.” 2011. Web. 04 Aug 2020.

Vancouver:

Moll JM. Structural characterisation of yeast Lsm protein complexes. [Internet] [Doctoral dissertation]. Macquarie University; 2011. [cited 2020 Aug 04]. Available from: http://hdl.handle.net/1959.14/192059.

Council of Science Editors:

Moll JM. Structural characterisation of yeast Lsm protein complexes. [Doctoral Dissertation]. Macquarie University; 2011. Available from: http://hdl.handle.net/1959.14/192059


Université Paris-Sud – Paris XI

30. Zahoor, Muhammad kashif. Genome wide analysis for novel regulators of growth and lipid metabolism in drosophila melanogaster : Cribles Post-Génomiques pour l’Identification de Régulateurs de la Croissance et du Métabolisme Lipidique chez la Drosophile.

Degree: Docteur es, Génétique, 2011, Université Paris-Sud – Paris XI

 Le réseau de signalisation qui répond à l’insuline et aux nutriments est conservé chez les métazoaires, où il joue un rôle central dans le contrôle… (more)

Subjects/Keywords: TOR kinase,; DS6 kinase; RNAi screen; Interaction protéine-protéine; Archipelago (Ago); Degradation de protéine; TOR kinase,; DS6 kinase; RNAi screen; Protein-protein interaction; Archipelago (Ago); Protein degradation

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APA (6th Edition):

Zahoor, M. k. (2011). Genome wide analysis for novel regulators of growth and lipid metabolism in drosophila melanogaster : Cribles Post-Génomiques pour l’Identification de Régulateurs de la Croissance et du Métabolisme Lipidique chez la Drosophile. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2011PA112039

Chicago Manual of Style (16th Edition):

Zahoor, Muhammad kashif. “Genome wide analysis for novel regulators of growth and lipid metabolism in drosophila melanogaster : Cribles Post-Génomiques pour l’Identification de Régulateurs de la Croissance et du Métabolisme Lipidique chez la Drosophile.” 2011. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed August 04, 2020. http://www.theses.fr/2011PA112039.

MLA Handbook (7th Edition):

Zahoor, Muhammad kashif. “Genome wide analysis for novel regulators of growth and lipid metabolism in drosophila melanogaster : Cribles Post-Génomiques pour l’Identification de Régulateurs de la Croissance et du Métabolisme Lipidique chez la Drosophile.” 2011. Web. 04 Aug 2020.

Vancouver:

Zahoor Mk. Genome wide analysis for novel regulators of growth and lipid metabolism in drosophila melanogaster : Cribles Post-Génomiques pour l’Identification de Régulateurs de la Croissance et du Métabolisme Lipidique chez la Drosophile. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2011. [cited 2020 Aug 04]. Available from: http://www.theses.fr/2011PA112039.

Council of Science Editors:

Zahoor Mk. Genome wide analysis for novel regulators of growth and lipid metabolism in drosophila melanogaster : Cribles Post-Génomiques pour l’Identification de Régulateurs de la Croissance et du Métabolisme Lipidique chez la Drosophile. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2011. Available from: http://www.theses.fr/2011PA112039

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