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You searched for subject:(Proteolysis). Showing records 1 – 30 of 264 total matches.

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University of Minnesota

1. Hayward, Amanda. Conformational Regulation of Cell Surface Receptor Proteolysis.

Degree: PhD, Biochemistry, Molecular Bio, and Biophysics, 2019, University of Minnesota

 Cell surface receptors can commonly undergo ectodomain shedding to modulate signaling pathways and cell contacts. To date, there are over 400 proteins that serve diverse… (more)

Subjects/Keywords: Juxtamembrane domain; Proteolysis

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APA (6th Edition):

Hayward, A. (2019). Conformational Regulation of Cell Surface Receptor Proteolysis. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/202420

Chicago Manual of Style (16th Edition):

Hayward, Amanda. “Conformational Regulation of Cell Surface Receptor Proteolysis.” 2019. Doctoral Dissertation, University of Minnesota. Accessed December 01, 2020. http://hdl.handle.net/11299/202420.

MLA Handbook (7th Edition):

Hayward, Amanda. “Conformational Regulation of Cell Surface Receptor Proteolysis.” 2019. Web. 01 Dec 2020.

Vancouver:

Hayward A. Conformational Regulation of Cell Surface Receptor Proteolysis. [Internet] [Doctoral dissertation]. University of Minnesota; 2019. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/11299/202420.

Council of Science Editors:

Hayward A. Conformational Regulation of Cell Surface Receptor Proteolysis. [Doctoral Dissertation]. University of Minnesota; 2019. Available from: http://hdl.handle.net/11299/202420


Cornell University

2. Laflamme, Brooke. Proteolysis Regulators In Drosophila Melanogaster Seminal Fluid.

Degree: PhD, Genetics, 2012, Cornell University

 In Drosophila melanogaster, seminal fluid proteins (Sfps) are transferred to females during mating and, together with sperm, are necessary for the many post-mating responses elicited… (more)

Subjects/Keywords: Drosophila; seminal fluid; proteolysis; protease

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APA (6th Edition):

Laflamme, B. (2012). Proteolysis Regulators In Drosophila Melanogaster Seminal Fluid. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/30983

Chicago Manual of Style (16th Edition):

Laflamme, Brooke. “Proteolysis Regulators In Drosophila Melanogaster Seminal Fluid.” 2012. Doctoral Dissertation, Cornell University. Accessed December 01, 2020. http://hdl.handle.net/1813/30983.

MLA Handbook (7th Edition):

Laflamme, Brooke. “Proteolysis Regulators In Drosophila Melanogaster Seminal Fluid.” 2012. Web. 01 Dec 2020.

Vancouver:

Laflamme B. Proteolysis Regulators In Drosophila Melanogaster Seminal Fluid. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/1813/30983.

Council of Science Editors:

Laflamme B. Proteolysis Regulators In Drosophila Melanogaster Seminal Fluid. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/30983

3. Boukais, Kamel. Activation et clairance transpariétales du plasminogène par les cellules musculaires lisses : applications à l'athérome et aux anévrismes de l'aorte ascendante : Transparietal activation and clearance of plasminogen by smooth muscle cells : application to atheroma and the aneurysms of the ascending aorta.

Degree: Docteur es, Médecine. Pathologie cardiovasculaire, 2016, Sorbonne Paris Cité

La protéolyse péricellulaire représente un phénomène commun à différentes pathologies vasculaires, notamment l’athérome et les anévrismes de l’aorte ascendante humaine (TAA). Le plasminogène est un… (more)

Subjects/Keywords: Protéolyse péricellulaire; Pericellular proteolysis

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APA (6th Edition):

Boukais, K. (2016). Activation et clairance transpariétales du plasminogène par les cellules musculaires lisses : applications à l'athérome et aux anévrismes de l'aorte ascendante : Transparietal activation and clearance of plasminogen by smooth muscle cells : application to atheroma and the aneurysms of the ascending aorta. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2016USPCC167

Chicago Manual of Style (16th Edition):

Boukais, Kamel. “Activation et clairance transpariétales du plasminogène par les cellules musculaires lisses : applications à l'athérome et aux anévrismes de l'aorte ascendante : Transparietal activation and clearance of plasminogen by smooth muscle cells : application to atheroma and the aneurysms of the ascending aorta.” 2016. Doctoral Dissertation, Sorbonne Paris Cité. Accessed December 01, 2020. http://www.theses.fr/2016USPCC167.

MLA Handbook (7th Edition):

Boukais, Kamel. “Activation et clairance transpariétales du plasminogène par les cellules musculaires lisses : applications à l'athérome et aux anévrismes de l'aorte ascendante : Transparietal activation and clearance of plasminogen by smooth muscle cells : application to atheroma and the aneurysms of the ascending aorta.” 2016. Web. 01 Dec 2020.

Vancouver:

Boukais K. Activation et clairance transpariétales du plasminogène par les cellules musculaires lisses : applications à l'athérome et aux anévrismes de l'aorte ascendante : Transparietal activation and clearance of plasminogen by smooth muscle cells : application to atheroma and the aneurysms of the ascending aorta. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2016. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2016USPCC167.

Council of Science Editors:

Boukais K. Activation et clairance transpariétales du plasminogène par les cellules musculaires lisses : applications à l'athérome et aux anévrismes de l'aorte ascendante : Transparietal activation and clearance of plasminogen by smooth muscle cells : application to atheroma and the aneurysms of the ascending aorta. [Doctoral Dissertation]. Sorbonne Paris Cité; 2016. Available from: http://www.theses.fr/2016USPCC167


University of Waikato

4. Fraser-Smith, Emma Louise. Characterizing the Catalytic Action of μ-Calpain on Myofibrillar Protein Structure .

Degree: 2006, University of Waikato

 Solving the problem of inconsistent meat tenderness is a top priority of the meat industry. This requires a greater understanding of the processes that affect… (more)

Subjects/Keywords: Calpain; proteolysis

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APA (6th Edition):

Fraser-Smith, E. L. (2006). Characterizing the Catalytic Action of μ-Calpain on Myofibrillar Protein Structure . (Masters Thesis). University of Waikato. Retrieved from http://hdl.handle.net/10289/2253

Chicago Manual of Style (16th Edition):

Fraser-Smith, Emma Louise. “Characterizing the Catalytic Action of μ-Calpain on Myofibrillar Protein Structure .” 2006. Masters Thesis, University of Waikato. Accessed December 01, 2020. http://hdl.handle.net/10289/2253.

MLA Handbook (7th Edition):

Fraser-Smith, Emma Louise. “Characterizing the Catalytic Action of μ-Calpain on Myofibrillar Protein Structure .” 2006. Web. 01 Dec 2020.

Vancouver:

Fraser-Smith EL. Characterizing the Catalytic Action of μ-Calpain on Myofibrillar Protein Structure . [Internet] [Masters thesis]. University of Waikato; 2006. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10289/2253.

Council of Science Editors:

Fraser-Smith EL. Characterizing the Catalytic Action of μ-Calpain on Myofibrillar Protein Structure . [Masters Thesis]. University of Waikato; 2006. Available from: http://hdl.handle.net/10289/2253


University of Illinois – Urbana-Champaign

5. Galloway, Hunter O'Neal. Characterizing meat tenderness of finishing steers fed for different rates of gain.

Degree: PhD, Animal Sciences, 2016, University of Illinois – Urbana-Champaign

 Objectives were to characterize effects of average daily gain (ADG) on Warner-Bratzler shear force (WBSF) and characterize effects of ADG on postmortem proteolysis in steers.… (more)

Subjects/Keywords: Proteolysis; Warner-Bratzler shear force

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APA (6th Edition):

Galloway, H. O. (2016). Characterizing meat tenderness of finishing steers fed for different rates of gain. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/90520

Chicago Manual of Style (16th Edition):

Galloway, Hunter O'Neal. “Characterizing meat tenderness of finishing steers fed for different rates of gain.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 01, 2020. http://hdl.handle.net/2142/90520.

MLA Handbook (7th Edition):

Galloway, Hunter O'Neal. “Characterizing meat tenderness of finishing steers fed for different rates of gain.” 2016. Web. 01 Dec 2020.

Vancouver:

Galloway HO. Characterizing meat tenderness of finishing steers fed for different rates of gain. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/2142/90520.

Council of Science Editors:

Galloway HO. Characterizing meat tenderness of finishing steers fed for different rates of gain. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/90520


University of Otago

6. Draper, Richard Charles. Divergent proteolysis of anti-sigma proteins controls cell-surface signalling in Pseudomonas aeruginosa .

Degree: 2013, University of Otago

 In cell-surface signalling pathways, the binding of an iron chelate to a specific outer membrane receptor induces gene expression in the cytoplasm via extra-cytoplasmic function… (more)

Subjects/Keywords: siderophore; pyoverdine; signalling; ECF; sigma; proteolysis; pseudomonas

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APA (6th Edition):

Draper, R. C. (2013). Divergent proteolysis of anti-sigma proteins controls cell-surface signalling in Pseudomonas aeruginosa . (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/3944

Chicago Manual of Style (16th Edition):

Draper, Richard Charles. “Divergent proteolysis of anti-sigma proteins controls cell-surface signalling in Pseudomonas aeruginosa .” 2013. Doctoral Dissertation, University of Otago. Accessed December 01, 2020. http://hdl.handle.net/10523/3944.

MLA Handbook (7th Edition):

Draper, Richard Charles. “Divergent proteolysis of anti-sigma proteins controls cell-surface signalling in Pseudomonas aeruginosa .” 2013. Web. 01 Dec 2020.

Vancouver:

Draper RC. Divergent proteolysis of anti-sigma proteins controls cell-surface signalling in Pseudomonas aeruginosa . [Internet] [Doctoral dissertation]. University of Otago; 2013. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10523/3944.

Council of Science Editors:

Draper RC. Divergent proteolysis of anti-sigma proteins controls cell-surface signalling in Pseudomonas aeruginosa . [Doctoral Dissertation]. University of Otago; 2013. Available from: http://hdl.handle.net/10523/3944


Cornell University

7. Portnoff, Alyse. Ubiquibodies: Engineered Ubiquitin Ligases With Unnatural Substrate Specificity For Targeted Protein Silencing.

Degree: PhD, Biomedical Engineering, 2014, Cornell University

 The ubiquitin-proteasome pathway (UPP) is the main route of protein degradation in eukaryotic cells and aids in regulation of cell cycle and cellular homeostasis. This… (more)

Subjects/Keywords: protein engineering; targeted proteolysis; reverse genetics

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APA (6th Edition):

Portnoff, A. (2014). Ubiquibodies: Engineered Ubiquitin Ligases With Unnatural Substrate Specificity For Targeted Protein Silencing. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/36040

Chicago Manual of Style (16th Edition):

Portnoff, Alyse. “Ubiquibodies: Engineered Ubiquitin Ligases With Unnatural Substrate Specificity For Targeted Protein Silencing.” 2014. Doctoral Dissertation, Cornell University. Accessed December 01, 2020. http://hdl.handle.net/1813/36040.

MLA Handbook (7th Edition):

Portnoff, Alyse. “Ubiquibodies: Engineered Ubiquitin Ligases With Unnatural Substrate Specificity For Targeted Protein Silencing.” 2014. Web. 01 Dec 2020.

Vancouver:

Portnoff A. Ubiquibodies: Engineered Ubiquitin Ligases With Unnatural Substrate Specificity For Targeted Protein Silencing. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/1813/36040.

Council of Science Editors:

Portnoff A. Ubiquibodies: Engineered Ubiquitin Ligases With Unnatural Substrate Specificity For Targeted Protein Silencing. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/36040


Harvard University

8. Zhang, Huadi. SPINT2 Suppresses Hippo Effector YAP and Limits Cellular Tolerance for Aneuploidy.

Degree: PhD, 2017, Harvard University

Oncogenic transformation is often accompanied by chromosome instability, an increased rate of chromosome missegregation. The consequent gain or loss of chromosomes—termed aneuploidy—hinders the growth of… (more)

Subjects/Keywords: Extracellular Proteolysis; Hippo Signaling; Chromosome Instability

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APA (6th Edition):

Zhang, H. (2017). SPINT2 Suppresses Hippo Effector YAP and Limits Cellular Tolerance for Aneuploidy. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061511

Chicago Manual of Style (16th Edition):

Zhang, Huadi. “SPINT2 Suppresses Hippo Effector YAP and Limits Cellular Tolerance for Aneuploidy.” 2017. Doctoral Dissertation, Harvard University. Accessed December 01, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061511.

MLA Handbook (7th Edition):

Zhang, Huadi. “SPINT2 Suppresses Hippo Effector YAP and Limits Cellular Tolerance for Aneuploidy.” 2017. Web. 01 Dec 2020.

Vancouver:

Zhang H. SPINT2 Suppresses Hippo Effector YAP and Limits Cellular Tolerance for Aneuploidy. [Internet] [Doctoral dissertation]. Harvard University; 2017. [cited 2020 Dec 01]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061511.

Council of Science Editors:

Zhang H. SPINT2 Suppresses Hippo Effector YAP and Limits Cellular Tolerance for Aneuploidy. [Doctoral Dissertation]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061511


University of Oxford

9. Fung, Ella. Fbxl13 regulates centrosome homeostasis and migration through ubiquitin mediated proteolysis.

Degree: PhD, 2017, University of Oxford

 Fbxl13 (F-box and leucine-rich repeat protein 13) is an orphan F-box protein. Fbox proteins are a family of substrate-targeting specificity factors for the SCF superfamily… (more)

Subjects/Keywords: 616.99; Oncology; centrosomes; F-box; ubiquitin; proteolysis

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APA (6th Edition):

Fung, E. (2017). Fbxl13 regulates centrosome homeostasis and migration through ubiquitin mediated proteolysis. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:5f0198b9-eea7-486f-9860-d006b9ed80e7 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.729160

Chicago Manual of Style (16th Edition):

Fung, Ella. “Fbxl13 regulates centrosome homeostasis and migration through ubiquitin mediated proteolysis.” 2017. Doctoral Dissertation, University of Oxford. Accessed December 01, 2020. http://ora.ox.ac.uk/objects/uuid:5f0198b9-eea7-486f-9860-d006b9ed80e7 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.729160.

MLA Handbook (7th Edition):

Fung, Ella. “Fbxl13 regulates centrosome homeostasis and migration through ubiquitin mediated proteolysis.” 2017. Web. 01 Dec 2020.

Vancouver:

Fung E. Fbxl13 regulates centrosome homeostasis and migration through ubiquitin mediated proteolysis. [Internet] [Doctoral dissertation]. University of Oxford; 2017. [cited 2020 Dec 01]. Available from: http://ora.ox.ac.uk/objects/uuid:5f0198b9-eea7-486f-9860-d006b9ed80e7 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.729160.

Council of Science Editors:

Fung E. Fbxl13 regulates centrosome homeostasis and migration through ubiquitin mediated proteolysis. [Doctoral Dissertation]. University of Oxford; 2017. Available from: http://ora.ox.ac.uk/objects/uuid:5f0198b9-eea7-486f-9860-d006b9ed80e7 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.729160


University of Southern California

10. Ngo, Jenny Kathleen. The human Lon protease in mitochondrial stress protection and aging.

Degree: PhD, Molecular Biology, 2008, University of Southern California

 The mitochondrial Lon protease was discovered in our laboratory to be the major protease that degrades oxidized mitochondrial proteins, specifically oxidized aconitase. Published work from… (more)

Subjects/Keywords: mitochondria; proteolysis; aging

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APA (6th Edition):

Ngo, J. K. (2008). The human Lon protease in mitochondrial stress protection and aging. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/85299/rec/6776

Chicago Manual of Style (16th Edition):

Ngo, Jenny Kathleen. “The human Lon protease in mitochondrial stress protection and aging.” 2008. Doctoral Dissertation, University of Southern California. Accessed December 01, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/85299/rec/6776.

MLA Handbook (7th Edition):

Ngo, Jenny Kathleen. “The human Lon protease in mitochondrial stress protection and aging.” 2008. Web. 01 Dec 2020.

Vancouver:

Ngo JK. The human Lon protease in mitochondrial stress protection and aging. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2020 Dec 01]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/85299/rec/6776.

Council of Science Editors:

Ngo JK. The human Lon protease in mitochondrial stress protection and aging. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/85299/rec/6776


University of South Florida

11. Krute, Christina Nadia. Investigation of Post-Translational Modifications in Staphylococcus aureus.

Degree: 2015, University of South Florida

 The work presented herein details post-translational modifications (PTMs) in Staphylococcus aureus that are involved in mediating the stress response and normal cellular processes. The first… (more)

Subjects/Keywords: HtrA; IspA; Prenylation; Proteolysis; PrsS; Stress; Microbiology

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APA (6th Edition):

Krute, C. N. (2015). Investigation of Post-Translational Modifications in Staphylococcus aureus. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/5719

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):

Krute, Christina Nadia. “Investigation of Post-Translational Modifications in Staphylococcus aureus.” 2015. Thesis, University of South Florida. Accessed December 01, 2020. https://scholarcommons.usf.edu/etd/5719.

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

MLA Handbook (7th Edition):

Krute, Christina Nadia. “Investigation of Post-Translational Modifications in Staphylococcus aureus.” 2015. Web. 01 Dec 2020.

Vancouver:

Krute CN. Investigation of Post-Translational Modifications in Staphylococcus aureus. [Internet] [Thesis]. University of South Florida; 2015. [cited 2020 Dec 01]. Available from: https://scholarcommons.usf.edu/etd/5719.

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

Council of Science Editors:

Krute CN. Investigation of Post-Translational Modifications in Staphylococcus aureus. [Thesis]. University of South Florida; 2015. Available from: https://scholarcommons.usf.edu/etd/5719

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


University of Florida

12. Wright, Shelby Ashlyn. Relating Muscle Fiber Morphometrics and Protein Degradation to Meat Quality in a Multibreed Herd.

Degree: MS, Animal Sciences, 2016, University of Florida

Subjects/Keywords: autolysis; brahman; proteolysis

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APA (6th Edition):

Wright, S. A. (2016). Relating Muscle Fiber Morphometrics and Protein Degradation to Meat Quality in a Multibreed Herd. (Masters Thesis). University of Florida. Retrieved from https://ufdc.ufl.edu/UFE0050757

Chicago Manual of Style (16th Edition):

Wright, Shelby Ashlyn. “Relating Muscle Fiber Morphometrics and Protein Degradation to Meat Quality in a Multibreed Herd.” 2016. Masters Thesis, University of Florida. Accessed December 01, 2020. https://ufdc.ufl.edu/UFE0050757.

MLA Handbook (7th Edition):

Wright, Shelby Ashlyn. “Relating Muscle Fiber Morphometrics and Protein Degradation to Meat Quality in a Multibreed Herd.” 2016. Web. 01 Dec 2020.

Vancouver:

Wright SA. Relating Muscle Fiber Morphometrics and Protein Degradation to Meat Quality in a Multibreed Herd. [Internet] [Masters thesis]. University of Florida; 2016. [cited 2020 Dec 01]. Available from: https://ufdc.ufl.edu/UFE0050757.

Council of Science Editors:

Wright SA. Relating Muscle Fiber Morphometrics and Protein Degradation to Meat Quality in a Multibreed Herd. [Masters Thesis]. University of Florida; 2016. Available from: https://ufdc.ufl.edu/UFE0050757


University of Sydney

13. Hamson, Elizabeth. Functional Characterisation and Outcomes of Post Translational Modifications Driven by Fibroblast Activation Protein Enzyme Activity .

Degree: 2015, University of Sydney

 Fibroblast Activation Protein (FAP) is a cellXsurface anchored dimeric protease, closely related to Dipeptidyl Peptidase (DPP) 4. This atypical serine protease has both dipeptidyl peptidase… (more)

Subjects/Keywords: proteomics; proteolysis; substrate; degradomics; enzyme; inflammation

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APA (6th Edition):

Hamson, E. (2015). Functional Characterisation and Outcomes of Post Translational Modifications Driven by Fibroblast Activation Protein Enzyme Activity . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/14891

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):

Hamson, Elizabeth. “Functional Characterisation and Outcomes of Post Translational Modifications Driven by Fibroblast Activation Protein Enzyme Activity .” 2015. Thesis, University of Sydney. Accessed December 01, 2020. http://hdl.handle.net/2123/14891.

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

MLA Handbook (7th Edition):

Hamson, Elizabeth. “Functional Characterisation and Outcomes of Post Translational Modifications Driven by Fibroblast Activation Protein Enzyme Activity .” 2015. Web. 01 Dec 2020.

Vancouver:

Hamson E. Functional Characterisation and Outcomes of Post Translational Modifications Driven by Fibroblast Activation Protein Enzyme Activity . [Internet] [Thesis]. University of Sydney; 2015. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/2123/14891.

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

Council of Science Editors:

Hamson E. Functional Characterisation and Outcomes of Post Translational Modifications Driven by Fibroblast Activation Protein Enzyme Activity . [Thesis]. University of Sydney; 2015. Available from: http://hdl.handle.net/2123/14891

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


University of Kentucky

14. Keesling, David C. INVESTIGATING THE PED PROTEIN AND ITS EFFECT ON TRANSLATIONAL CONTROL IN DROSOPHILA MELANOGASTER SPERMATOGENESIS.

Degree: 2012, University of Kentucky

 Inactive mutants of the ped gene cause two phenotypes in Drosophila melanogaster: male sterility and the early translation of DHODH within spermatogenesis. Investigation of the… (more)

Subjects/Keywords: translational control; deubiquitination; spermatogenesis; otubain; proteolysis; Biology

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APA (6th Edition):

Keesling, D. C. (2012). INVESTIGATING THE PED PROTEIN AND ITS EFFECT ON TRANSLATIONAL CONTROL IN DROSOPHILA MELANOGASTER SPERMATOGENESIS. (Masters Thesis). University of Kentucky. Retrieved from https://uknowledge.uky.edu/biology_etds/2

Chicago Manual of Style (16th Edition):

Keesling, David C. “INVESTIGATING THE PED PROTEIN AND ITS EFFECT ON TRANSLATIONAL CONTROL IN DROSOPHILA MELANOGASTER SPERMATOGENESIS.” 2012. Masters Thesis, University of Kentucky. Accessed December 01, 2020. https://uknowledge.uky.edu/biology_etds/2.

MLA Handbook (7th Edition):

Keesling, David C. “INVESTIGATING THE PED PROTEIN AND ITS EFFECT ON TRANSLATIONAL CONTROL IN DROSOPHILA MELANOGASTER SPERMATOGENESIS.” 2012. Web. 01 Dec 2020.

Vancouver:

Keesling DC. INVESTIGATING THE PED PROTEIN AND ITS EFFECT ON TRANSLATIONAL CONTROL IN DROSOPHILA MELANOGASTER SPERMATOGENESIS. [Internet] [Masters thesis]. University of Kentucky; 2012. [cited 2020 Dec 01]. Available from: https://uknowledge.uky.edu/biology_etds/2.

Council of Science Editors:

Keesling DC. INVESTIGATING THE PED PROTEIN AND ITS EFFECT ON TRANSLATIONAL CONTROL IN DROSOPHILA MELANOGASTER SPERMATOGENESIS. [Masters Thesis]. University of Kentucky; 2012. Available from: https://uknowledge.uky.edu/biology_etds/2

15. Cantin, Amber M. Proteolytic Regulation of CtrA, the Master Regulator of Cell Cycle in Caulobacter crescentus.

Degree: MS, Biochemistry, 2012, University of Massachusetts

  Cell cycle progression in Caulobacter crescentus depends on the master regulator, CtrA. During the transition from swarmer to stalk cell (G1 to S phase),… (more)

Subjects/Keywords: Caulobacter; proteolysis; CtrA; SciP; Biochemistry; Molecular Biology

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APA (6th Edition):

Cantin, A. M. (2012). Proteolytic Regulation of CtrA, the Master Regulator of Cell Cycle in Caulobacter crescentus. (Masters Thesis). University of Massachusetts. Retrieved from https://scholarworks.umass.edu/theses/896

Chicago Manual of Style (16th Edition):

Cantin, Amber M. “Proteolytic Regulation of CtrA, the Master Regulator of Cell Cycle in Caulobacter crescentus.” 2012. Masters Thesis, University of Massachusetts. Accessed December 01, 2020. https://scholarworks.umass.edu/theses/896.

MLA Handbook (7th Edition):

Cantin, Amber M. “Proteolytic Regulation of CtrA, the Master Regulator of Cell Cycle in Caulobacter crescentus.” 2012. Web. 01 Dec 2020.

Vancouver:

Cantin AM. Proteolytic Regulation of CtrA, the Master Regulator of Cell Cycle in Caulobacter crescentus. [Internet] [Masters thesis]. University of Massachusetts; 2012. [cited 2020 Dec 01]. Available from: https://scholarworks.umass.edu/theses/896.

Council of Science Editors:

Cantin AM. Proteolytic Regulation of CtrA, the Master Regulator of Cell Cycle in Caulobacter crescentus. [Masters Thesis]. University of Massachusetts; 2012. Available from: https://scholarworks.umass.edu/theses/896


University of Helsinki

16. Judström, Ilona. The Physiological Effect of Mouse Peritoneal Mast Cell Chymase Activity on High Density Lipoproteins.

Degree: Department of Basic Veterinary Sciences; Helsingin yliopisto, Eläinlääketieteellinen tiedekunta, Peruseläinlääketieteen laitos; Helsingfors universitet, Veterinärmedicinska fakulteten, Institutionen för basveterinärmedicin, 2009, University of Helsinki

 In atherosclerosis, cholesterol accumulates in cholesterol-loaded macrophages (foam cells) forming cholesterol plaques in the arterial intima. Reverse cholesterol transport (RCT) is a mechanism in which… (more)

Subjects/Keywords: chymase; cholesterol efflux; foam cells; macrophages; proteolysis; atherosclerosis; Patologia; Patologi; Pathology; chymase; cholesterol efflux; foam cells; macrophages; proteolysis; atherosclerosis

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APA (6th Edition):

Judström, I. (2009). The Physiological Effect of Mouse Peritoneal Mast Cell Chymase Activity on High Density Lipoproteins. (Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/14585

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):

Judström, Ilona. “The Physiological Effect of Mouse Peritoneal Mast Cell Chymase Activity on High Density Lipoproteins.” 2009. Thesis, University of Helsinki. Accessed December 01, 2020. http://hdl.handle.net/10138/14585.

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

MLA Handbook (7th Edition):

Judström, Ilona. “The Physiological Effect of Mouse Peritoneal Mast Cell Chymase Activity on High Density Lipoproteins.” 2009. Web. 01 Dec 2020.

Vancouver:

Judström I. The Physiological Effect of Mouse Peritoneal Mast Cell Chymase Activity on High Density Lipoproteins. [Internet] [Thesis]. University of Helsinki; 2009. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10138/14585.

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

Council of Science Editors:

Judström I. The Physiological Effect of Mouse Peritoneal Mast Cell Chymase Activity on High Density Lipoproteins. [Thesis]. University of Helsinki; 2009. Available from: http://hdl.handle.net/10138/14585

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


University of California – Berkeley

17. Smith, Stephen Carl. A novel adapter mechanism regulates the Caulobacter cell cycle by promoting the degradation of the transcriptional regulator CtrA.

Degree: Microbiology, 2013, University of California – Berkeley

 Caulobacter crescentus is a powerful model organism for understanding cellular differentiation, cell polarity and cell cycle regulation in bacteria. An elaborate network of two-component signaling… (more)

Subjects/Keywords: Microbiology; Caulobacter; cell cycle; ClpXP; CtrA; cyclic diguanylate; Proteolysis

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APA (6th Edition):

Smith, S. C. (2013). A novel adapter mechanism regulates the Caulobacter cell cycle by promoting the degradation of the transcriptional regulator CtrA. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/7f234361

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, Stephen Carl. “A novel adapter mechanism regulates the Caulobacter cell cycle by promoting the degradation of the transcriptional regulator CtrA.” 2013. Thesis, University of California – Berkeley. Accessed December 01, 2020. http://www.escholarship.org/uc/item/7f234361.

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

MLA Handbook (7th Edition):

Smith, Stephen Carl. “A novel adapter mechanism regulates the Caulobacter cell cycle by promoting the degradation of the transcriptional regulator CtrA.” 2013. Web. 01 Dec 2020.

Vancouver:

Smith SC. A novel adapter mechanism regulates the Caulobacter cell cycle by promoting the degradation of the transcriptional regulator CtrA. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2020 Dec 01]. Available from: http://www.escholarship.org/uc/item/7f234361.

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

Council of Science Editors:

Smith SC. A novel adapter mechanism regulates the Caulobacter cell cycle by promoting the degradation of the transcriptional regulator CtrA. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/7f234361

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

18. Silva, Gustavo Monteiro. Estudo e caracterização do processo de glutatiolação e desglutatiolação da unidade 20S do proteassomo da levedura Saccharomyces cerevisiae: Implicações na regulação do metabolismo redox intracelular e na geração de peptídeos.

Degree: PhD, Biologia (Genética), 2010, University of São Paulo

O proteassomo é o componente do sistema Ubiquitina-Proteassomo (UPS), responsável pela degradação de proteínas intracelulares marcadas com cauda de ubiquitina. No entanto, a unidade catalítica… (more)

Subjects/Keywords: Glutathiolation; Glutatiolação; Metabolismo Redox; Proteasome; Proteassomo; Proteólise; Proteolysis; Redox Metabolism

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APA (6th Edition):

Silva, G. M. (2010). Estudo e caracterização do processo de glutatiolação e desglutatiolação da unidade 20S do proteassomo da levedura Saccharomyces cerevisiae: Implicações na regulação do metabolismo redox intracelular e na geração de peptídeos. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/41/41131/tde-25112010-122339/ ;

Chicago Manual of Style (16th Edition):

Silva, Gustavo Monteiro. “Estudo e caracterização do processo de glutatiolação e desglutatiolação da unidade 20S do proteassomo da levedura Saccharomyces cerevisiae: Implicações na regulação do metabolismo redox intracelular e na geração de peptídeos.” 2010. Doctoral Dissertation, University of São Paulo. Accessed December 01, 2020. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-25112010-122339/ ;.

MLA Handbook (7th Edition):

Silva, Gustavo Monteiro. “Estudo e caracterização do processo de glutatiolação e desglutatiolação da unidade 20S do proteassomo da levedura Saccharomyces cerevisiae: Implicações na regulação do metabolismo redox intracelular e na geração de peptídeos.” 2010. Web. 01 Dec 2020.

Vancouver:

Silva GM. Estudo e caracterização do processo de glutatiolação e desglutatiolação da unidade 20S do proteassomo da levedura Saccharomyces cerevisiae: Implicações na regulação do metabolismo redox intracelular e na geração de peptídeos. [Internet] [Doctoral dissertation]. University of São Paulo; 2010. [cited 2020 Dec 01]. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-25112010-122339/ ;.

Council of Science Editors:

Silva GM. Estudo e caracterização do processo de glutatiolação e desglutatiolação da unidade 20S do proteassomo da levedura Saccharomyces cerevisiae: Implicações na regulação do metabolismo redox intracelular e na geração de peptídeos. [Doctoral Dissertation]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-25112010-122339/ ;

19. Dickey, Seth W. Rhomboid Proteolysis is a Rate-Governed Reaction, Yet is Dispensable for E. coli Colonization of the Mouse Colon.

Degree: 2013, Johns Hopkins University

Proteolysis, the controlled dissection of proteins into two parts, is essential to all life. Intramembrane proteolysis, whereby specialized enzymes cut membrane-resident segments, extends this potent… (more)

Subjects/Keywords: Rhomboid; Rhomboid Protease; Intramembrane; Intramembrane Protease; Proteolysis; Kinetics; Membrane; Lipid Bilayer

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APA (6th Edition):

Dickey, S. W. (2013). Rhomboid Proteolysis is a Rate-Governed Reaction, Yet is Dispensable for E. coli Colonization of the Mouse Colon. (Thesis). Johns Hopkins University. Retrieved from http://jhir.library.jhu.edu/handle/1774.2/37836

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):

Dickey, Seth W. “Rhomboid Proteolysis is a Rate-Governed Reaction, Yet is Dispensable for E. coli Colonization of the Mouse Colon.” 2013. Thesis, Johns Hopkins University. Accessed December 01, 2020. http://jhir.library.jhu.edu/handle/1774.2/37836.

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

MLA Handbook (7th Edition):

Dickey, Seth W. “Rhomboid Proteolysis is a Rate-Governed Reaction, Yet is Dispensable for E. coli Colonization of the Mouse Colon.” 2013. Web. 01 Dec 2020.

Vancouver:

Dickey SW. Rhomboid Proteolysis is a Rate-Governed Reaction, Yet is Dispensable for E. coli Colonization of the Mouse Colon. [Internet] [Thesis]. Johns Hopkins University; 2013. [cited 2020 Dec 01]. Available from: http://jhir.library.jhu.edu/handle/1774.2/37836.

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

Council of Science Editors:

Dickey SW. Rhomboid Proteolysis is a Rate-Governed Reaction, Yet is Dispensable for E. coli Colonization of the Mouse Colon. [Thesis]. Johns Hopkins University; 2013. Available from: http://jhir.library.jhu.edu/handle/1774.2/37836

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

20. Beri, Despina. Μοριακή και λειτουργική ανάλυση αναπτυξιακών γονιδίων στο Arobidopsis thaliana.

Degree: 2016, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

 The WD40 motif, or beta-transducin repeat (WDR), is considered one of the most abundant domains among the eukaryotic proteins, while it is rarely found in… (more)

Subjects/Keywords: WD40 πρωτεΐνες; Πρωτεόλυση; Κυτταρικό τοίχωμα; WD40 proteins; Proteolysis; Cell wall

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APA (6th Edition):

Beri, D. (2016). Μοριακή και λειτουργική ανάλυση αναπτυξιακών γονιδίων στο Arobidopsis thaliana. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/38974

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):

Beri, Despina. “Μοριακή και λειτουργική ανάλυση αναπτυξιακών γονιδίων στο Arobidopsis thaliana.” 2016. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed December 01, 2020. http://hdl.handle.net/10442/hedi/38974.

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

MLA Handbook (7th Edition):

Beri, Despina. “Μοριακή και λειτουργική ανάλυση αναπτυξιακών γονιδίων στο Arobidopsis thaliana.” 2016. Web. 01 Dec 2020.

Vancouver:

Beri D. Μοριακή και λειτουργική ανάλυση αναπτυξιακών γονιδίων στο Arobidopsis thaliana. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2016. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10442/hedi/38974.

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

Council of Science Editors:

Beri D. Μοριακή και λειτουργική ανάλυση αναπτυξιακών γονιδίων στο Arobidopsis thaliana. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2016. Available from: http://hdl.handle.net/10442/hedi/38974

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


University of Manchester

21. Quinn, James. Tau proteolysis mechanisms and relevance for tauopathies.

Degree: 2019, University of Manchester

 Neurodegenerative diseases with tau inclusions in the brain are classified as tauopathies; 28 of these exist and typically present with dementia or parkinsonism symptoms. During… (more)

Subjects/Keywords: Dementia; Tau; Neurodegeneration; Granzyme A; Proteolytic cleavage; Proteolysis; Biomarker; Tauopathies

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APA (6th Edition):

Quinn, J. (2019). Tau proteolysis mechanisms and relevance for tauopathies. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:317977

Chicago Manual of Style (16th Edition):

Quinn, James. “Tau proteolysis mechanisms and relevance for tauopathies.” 2019. Doctoral Dissertation, University of Manchester. Accessed December 01, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:317977.

MLA Handbook (7th Edition):

Quinn, James. “Tau proteolysis mechanisms and relevance for tauopathies.” 2019. Web. 01 Dec 2020.

Vancouver:

Quinn J. Tau proteolysis mechanisms and relevance for tauopathies. [Internet] [Doctoral dissertation]. University of Manchester; 2019. [cited 2020 Dec 01]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:317977.

Council of Science Editors:

Quinn J. Tau proteolysis mechanisms and relevance for tauopathies. [Doctoral Dissertation]. University of Manchester; 2019. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:317977


Jawaharlal Nehru University

22. Balajee, S R. Peptide ligation and protei assemblage by reverse proteolysis; -.

Degree: Immunology, 2003, Jawaharlal Nehru University

None

Bibilography p.58-76

Advisors/Committee Members: Roy, R P.

Subjects/Keywords: Immunology; Peptide; assemblage; proteolysis; protein

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APA (6th Edition):

Balajee, S. R. (2003). Peptide ligation and protei assemblage by reverse proteolysis; -. (Thesis). Jawaharlal Nehru University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/19406

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):

Balajee, S R. “Peptide ligation and protei assemblage by reverse proteolysis; -.” 2003. Thesis, Jawaharlal Nehru University. Accessed December 01, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/19406.

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

MLA Handbook (7th Edition):

Balajee, S R. “Peptide ligation and protei assemblage by reverse proteolysis; -.” 2003. Web. 01 Dec 2020.

Vancouver:

Balajee SR. Peptide ligation and protei assemblage by reverse proteolysis; -. [Internet] [Thesis]. Jawaharlal Nehru University; 2003. [cited 2020 Dec 01]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19406.

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

Council of Science Editors:

Balajee SR. Peptide ligation and protei assemblage by reverse proteolysis; -. [Thesis]. Jawaharlal Nehru University; 2003. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19406

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


Universidade Federal de Viçosa

23. Solimar Gonçalves Machado. Detecção de Pseudomonas fluorescens em leite cru pela reação em cadeia da polimerase.

Degree: 2011, Universidade Federal de Viçosa

Among the psychrotrophic micro-organisms that are able to grow during refrigeration, some of them produce thermostable proteases which can cause many technological problems in the… (more)

Subjects/Keywords: Psicotróficos; Proteólise; PCR; MICROBIOLOGIA DE ALIMENTOS; Psychrotrophic; Proteolysis; PCR

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APA (6th Edition):

Machado, S. G. (2011). Detecção de Pseudomonas fluorescens em leite cru pela reação em cadeia da polimerase. (Thesis). Universidade Federal de Viçosa. Retrieved from http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=3631

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):

Machado, Solimar Gonçalves. “Detecção de Pseudomonas fluorescens em leite cru pela reação em cadeia da polimerase.” 2011. Thesis, Universidade Federal de Viçosa. Accessed December 01, 2020. http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=3631.

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

MLA Handbook (7th Edition):

Machado, Solimar Gonçalves. “Detecção de Pseudomonas fluorescens em leite cru pela reação em cadeia da polimerase.” 2011. Web. 01 Dec 2020.

Vancouver:

Machado SG. Detecção de Pseudomonas fluorescens em leite cru pela reação em cadeia da polimerase. [Internet] [Thesis]. Universidade Federal de Viçosa; 2011. [cited 2020 Dec 01]. Available from: http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=3631.

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

Council of Science Editors:

Machado SG. Detecção de Pseudomonas fluorescens em leite cru pela reação em cadeia da polimerase. [Thesis]. Universidade Federal de Viçosa; 2011. Available from: http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=3631

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


McMaster University

24. Ahsan, Bilal. UNDERSTANDING THE ACTIVATION OF BACTERIAL PROTEASE CLPP BY ACYLDEPSIPEPTIDE ANTIBIOTIC.

Degree: MSc, 2014, McMaster University

Acyldepsipeptide (ADEP1) is an antibiotic that binds to Escherichia coli ClpP, mimicking the interaction that the protease typically establishes with ClpA/ClpX ATPases in bacterial cells.… (more)

Subjects/Keywords: ADEP; ClpP; ClpAP; Axial channel; ATP-independent proteolysis

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APA (6th Edition):

Ahsan, B. (2014). UNDERSTANDING THE ACTIVATION OF BACTERIAL PROTEASE CLPP BY ACYLDEPSIPEPTIDE ANTIBIOTIC. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/15947

Chicago Manual of Style (16th Edition):

Ahsan, Bilal. “UNDERSTANDING THE ACTIVATION OF BACTERIAL PROTEASE CLPP BY ACYLDEPSIPEPTIDE ANTIBIOTIC.” 2014. Masters Thesis, McMaster University. Accessed December 01, 2020. http://hdl.handle.net/11375/15947.

MLA Handbook (7th Edition):

Ahsan, Bilal. “UNDERSTANDING THE ACTIVATION OF BACTERIAL PROTEASE CLPP BY ACYLDEPSIPEPTIDE ANTIBIOTIC.” 2014. Web. 01 Dec 2020.

Vancouver:

Ahsan B. UNDERSTANDING THE ACTIVATION OF BACTERIAL PROTEASE CLPP BY ACYLDEPSIPEPTIDE ANTIBIOTIC. [Internet] [Masters thesis]. McMaster University; 2014. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/11375/15947.

Council of Science Editors:

Ahsan B. UNDERSTANDING THE ACTIVATION OF BACTERIAL PROTEASE CLPP BY ACYLDEPSIPEPTIDE ANTIBIOTIC. [Masters Thesis]. McMaster University; 2014. Available from: http://hdl.handle.net/11375/15947


Queens University

25. Hogan-Cann, Andrew. Proteolytic Cleavage of the Kv1.5 Channel in the S1-S2 Linker Does Not Affect Channel Function .

Degree: Physiology, 2015, Queens University

 Atrial fibrillation (AF), the most prevalent human cardiac arrhythmia, is characterized by rapid and disorderly electrical activity in the atria of the heart. Kv1.5 channel… (more)

Subjects/Keywords: electrophysiology ; Voltage-gated potassium channel ; Cell-surface protein ; Trafficking ; Proteolysis ; Kv1.5

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APA (6th Edition):

Hogan-Cann, A. (2015). Proteolytic Cleavage of the Kv1.5 Channel in the S1-S2 Linker Does Not Affect Channel Function . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/13500

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):

Hogan-Cann, Andrew. “Proteolytic Cleavage of the Kv1.5 Channel in the S1-S2 Linker Does Not Affect Channel Function .” 2015. Thesis, Queens University. Accessed December 01, 2020. http://hdl.handle.net/1974/13500.

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

MLA Handbook (7th Edition):

Hogan-Cann, Andrew. “Proteolytic Cleavage of the Kv1.5 Channel in the S1-S2 Linker Does Not Affect Channel Function .” 2015. Web. 01 Dec 2020.

Vancouver:

Hogan-Cann A. Proteolytic Cleavage of the Kv1.5 Channel in the S1-S2 Linker Does Not Affect Channel Function . [Internet] [Thesis]. Queens University; 2015. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/1974/13500.

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

Council of Science Editors:

Hogan-Cann A. Proteolytic Cleavage of the Kv1.5 Channel in the S1-S2 Linker Does Not Affect Channel Function . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/13500

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


University of California – Riverside

26. Duan, Yaokai. Fluorescence Labeling and Limited Proteolysis for Demystifying Protein Corona.

Degree: Chemistry, 2018, University of California – Riverside

 Engineered nanomaterials (ENMs) have great application potentials in biological systems, while the protein corona formed around ENMs after they encounter any biofluids makes their fate… (more)

Subjects/Keywords: Analytical chemistry; Fluorescence; Limited proteolysis; Mass spec; Nanomaterial; Protein

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APA (6th Edition):

Duan, Y. (2018). Fluorescence Labeling and Limited Proteolysis for Demystifying Protein Corona. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/2xj088r2

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):

Duan, Yaokai. “Fluorescence Labeling and Limited Proteolysis for Demystifying Protein Corona.” 2018. Thesis, University of California – Riverside. Accessed December 01, 2020. http://www.escholarship.org/uc/item/2xj088r2.

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

MLA Handbook (7th Edition):

Duan, Yaokai. “Fluorescence Labeling and Limited Proteolysis for Demystifying Protein Corona.” 2018. Web. 01 Dec 2020.

Vancouver:

Duan Y. Fluorescence Labeling and Limited Proteolysis for Demystifying Protein Corona. [Internet] [Thesis]. University of California – Riverside; 2018. [cited 2020 Dec 01]. Available from: http://www.escholarship.org/uc/item/2xj088r2.

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

Council of Science Editors:

Duan Y. Fluorescence Labeling and Limited Proteolysis for Demystifying Protein Corona. [Thesis]. University of California – Riverside; 2018. Available from: http://www.escholarship.org/uc/item/2xj088r2

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


Wayne State University

27. Victor, Bernadette Caroline. Functional in vitro analyses of lipid raft-associated cathepsin b: implication for the invasive phenotype of inflammatory breast cancer.

Degree: PhD, Cancer Biology, 2011, Wayne State University

  FUNCTIONAL IN VITRO ANALYSES OF LIPID RAFT-ASSOCIATED CATHEPSIN B: IMPLICATION FOR THE INVASIVE PHENOTYPE OF INFLAMMATORY BREAST CANCER by BERNADETTE C. VICTOR December 2011… (more)

Subjects/Keywords: cathepsin B, caveolae, inflammatory breast cancer, invasion, proteolysis; Cell Biology

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APA (6th Edition):

Victor, B. C. (2011). Functional in vitro analyses of lipid raft-associated cathepsin b: implication for the invasive phenotype of inflammatory breast cancer. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/400

Chicago Manual of Style (16th Edition):

Victor, Bernadette Caroline. “Functional in vitro analyses of lipid raft-associated cathepsin b: implication for the invasive phenotype of inflammatory breast cancer.” 2011. Doctoral Dissertation, Wayne State University. Accessed December 01, 2020. https://digitalcommons.wayne.edu/oa_dissertations/400.

MLA Handbook (7th Edition):

Victor, Bernadette Caroline. “Functional in vitro analyses of lipid raft-associated cathepsin b: implication for the invasive phenotype of inflammatory breast cancer.” 2011. Web. 01 Dec 2020.

Vancouver:

Victor BC. Functional in vitro analyses of lipid raft-associated cathepsin b: implication for the invasive phenotype of inflammatory breast cancer. [Internet] [Doctoral dissertation]. Wayne State University; 2011. [cited 2020 Dec 01]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/400.

Council of Science Editors:

Victor BC. Functional in vitro analyses of lipid raft-associated cathepsin b: implication for the invasive phenotype of inflammatory breast cancer. [Doctoral Dissertation]. Wayne State University; 2011. Available from: https://digitalcommons.wayne.edu/oa_dissertations/400


University of Texas Southwestern Medical Center

28. Shah, Sanjiv. Intramembrane Proteolysis Mediated by the gamma-Secretase Complex : Nicastrin Functions as a Substrate Receptor.

Degree: 2006, University of Texas Southwestern Medical Center

 The proteolytic processing of proteins within the lipid bilayer, and release of their membrane tethered biologically active fragments, fundamentally controls a growing list of cell… (more)

Subjects/Keywords: Membrane Proteins; Hydrolysis; Proteolysis

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

APA (6th Edition):

Shah, S. (2006). Intramembrane Proteolysis Mediated by the gamma-Secretase Complex : Nicastrin Functions as a Substrate Receptor. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/410

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):

Shah, Sanjiv. “Intramembrane Proteolysis Mediated by the gamma-Secretase Complex : Nicastrin Functions as a Substrate Receptor.” 2006. Thesis, University of Texas Southwestern Medical Center. Accessed December 01, 2020. http://hdl.handle.net/2152.5/410.

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

MLA Handbook (7th Edition):

Shah, Sanjiv. “Intramembrane Proteolysis Mediated by the gamma-Secretase Complex : Nicastrin Functions as a Substrate Receptor.” 2006. Web. 01 Dec 2020.

Vancouver:

Shah S. Intramembrane Proteolysis Mediated by the gamma-Secretase Complex : Nicastrin Functions as a Substrate Receptor. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2006. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/2152.5/410.

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

Council of Science Editors:

Shah S. Intramembrane Proteolysis Mediated by the gamma-Secretase Complex : Nicastrin Functions as a Substrate Receptor. [Thesis]. University of Texas Southwestern Medical Center; 2006. Available from: http://hdl.handle.net/2152.5/410

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


University of Texas Southwestern Medical Center

29. Morris, Lindsey LaChelle. Sequential Actions of VCP/p97 and the Proteasome 19S Regulatory Particle in Sterol-Accelerated, ER-Associated Degradation of HMG CoA Reductase.

Degree: 2014, University of Texas Southwestern Medical Center

 Accelerated endoplasmic reticulum (ER)-associated degradation (ERAD) of the cholesterol biosynthetic enzyme HMG CoA reductase results from its sterol-induced binding to ER membrane proteins called Insig-1… (more)

Subjects/Keywords: Adenosine Triphosphatases; Endoplasmic Reticulum; Hydroxymethylglutaryl CoA Reductases; Metalloendopeptidases; Proteolysis; Sterols

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

APA (6th Edition):

Morris, L. L. (2014). Sequential Actions of VCP/p97 and the Proteasome 19S Regulatory Particle in Sterol-Accelerated, ER-Associated Degradation of HMG CoA Reductase. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/3571

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):

Morris, Lindsey LaChelle. “Sequential Actions of VCP/p97 and the Proteasome 19S Regulatory Particle in Sterol-Accelerated, ER-Associated Degradation of HMG CoA Reductase.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed December 01, 2020. http://hdl.handle.net/2152.5/3571.

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

MLA Handbook (7th Edition):

Morris, Lindsey LaChelle. “Sequential Actions of VCP/p97 and the Proteasome 19S Regulatory Particle in Sterol-Accelerated, ER-Associated Degradation of HMG CoA Reductase.” 2014. Web. 01 Dec 2020.

Vancouver:

Morris LL. Sequential Actions of VCP/p97 and the Proteasome 19S Regulatory Particle in Sterol-Accelerated, ER-Associated Degradation of HMG CoA Reductase. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/2152.5/3571.

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

Council of Science Editors:

Morris LL. Sequential Actions of VCP/p97 and the Proteasome 19S Regulatory Particle in Sterol-Accelerated, ER-Associated Degradation of HMG CoA Reductase. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/3571

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


University of Texas Southwestern Medical Center

30. Archer, Chase Tanner. Modulation of Transcription Factor Activity by Mono-Ubiquitin.

Degree: 2008, University of Texas Southwestern Medical Center

 The Ubiquitin-Proteasome Pathway plays both proteolytic and non-proteolytic roles in the regulation of transcription. We recently reported that the ATPases of the 26S proteasome can… (more)

Subjects/Keywords: Ubiquitin; Proteolysis; Transcription Factors

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

APA (6th Edition):

Archer, C. T. (2008). Modulation of Transcription Factor Activity by Mono-Ubiquitin. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/310

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):

Archer, Chase Tanner. “Modulation of Transcription Factor Activity by Mono-Ubiquitin.” 2008. Thesis, University of Texas Southwestern Medical Center. Accessed December 01, 2020. http://hdl.handle.net/2152.5/310.

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

MLA Handbook (7th Edition):

Archer, Chase Tanner. “Modulation of Transcription Factor Activity by Mono-Ubiquitin.” 2008. Web. 01 Dec 2020.

Vancouver:

Archer CT. Modulation of Transcription Factor Activity by Mono-Ubiquitin. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2008. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/2152.5/310.

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

Council of Science Editors:

Archer CT. Modulation of Transcription Factor Activity by Mono-Ubiquitin. [Thesis]. University of Texas Southwestern Medical Center; 2008. Available from: http://hdl.handle.net/2152.5/310

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

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