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You searched for subject:(Chaperones). Showing records 1 – 30 of 303 total matches.

[1] [2] [3] [4] [5] … [11]

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Rutgers University

1. Chen, Li. Structural analyses of chaperone-substrate interactions in Type III secretion systems.

Degree: PhD, Chemistry and Chemical Biology, 2011, Rutgers University

The type III secretion system (TTSS) is used by many Gram-negative bacteria to inject virulence proteins across lipid membranes directly into the cytoplasm of eukaryotic… (more)

Subjects/Keywords: Molecular chaperones

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APA (6th Edition):

Chen, L. (2011). Structural analyses of chaperone-substrate interactions in Type III secretion systems. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061170

Chicago Manual of Style (16th Edition):

Chen, Li. “Structural analyses of chaperone-substrate interactions in Type III secretion systems.” 2011. Doctoral Dissertation, Rutgers University. Accessed January 19, 2021. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061170.

MLA Handbook (7th Edition):

Chen, Li. “Structural analyses of chaperone-substrate interactions in Type III secretion systems.” 2011. Web. 19 Jan 2021.

Vancouver:

Chen L. Structural analyses of chaperone-substrate interactions in Type III secretion systems. [Internet] [Doctoral dissertation]. Rutgers University; 2011. [cited 2021 Jan 19]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061170.

Council of Science Editors:

Chen L. Structural analyses of chaperone-substrate interactions in Type III secretion systems. [Doctoral Dissertation]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061170


Penn State University

2. Lewis, Carrie Rebekah. THE REGULATION OF ER CHAPERONES AND PROINSULIN PROTEOSTASIS BY PERK EIF2ALPHA KINASE.

Degree: 2016, Penn State University

 Insulin synthesis and secretion are finely controlled within the pancreatic β cell. Minor changes in circulating levels of insulin can elicit a major perturbance of… (more)

Subjects/Keywords: proinsulin; ER chaperones; PERK; EIF2AK3

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APA (6th Edition):

Lewis, C. R. (2016). THE REGULATION OF ER CHAPERONES AND PROINSULIN PROTEOSTASIS BY PERK EIF2ALPHA KINASE. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/bg257f046

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):

Lewis, Carrie Rebekah. “THE REGULATION OF ER CHAPERONES AND PROINSULIN PROTEOSTASIS BY PERK EIF2ALPHA KINASE.” 2016. Thesis, Penn State University. Accessed January 19, 2021. https://submit-etda.libraries.psu.edu/catalog/bg257f046.

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

MLA Handbook (7th Edition):

Lewis, Carrie Rebekah. “THE REGULATION OF ER CHAPERONES AND PROINSULIN PROTEOSTASIS BY PERK EIF2ALPHA KINASE.” 2016. Web. 19 Jan 2021.

Vancouver:

Lewis CR. THE REGULATION OF ER CHAPERONES AND PROINSULIN PROTEOSTASIS BY PERK EIF2ALPHA KINASE. [Internet] [Thesis]. Penn State University; 2016. [cited 2021 Jan 19]. Available from: https://submit-etda.libraries.psu.edu/catalog/bg257f046.

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

Council of Science Editors:

Lewis CR. THE REGULATION OF ER CHAPERONES AND PROINSULIN PROTEOSTASIS BY PERK EIF2ALPHA KINASE. [Thesis]. Penn State University; 2016. Available from: https://submit-etda.libraries.psu.edu/catalog/bg257f046

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


McMaster University

3. Shanmuganathan, Meera. High-Quality Screening of Pharmacological Chaperones for Enzyme Enhancement Therapy.

Degree: 2015, McMaster University

Enzyme enhancement therapy based on pharmacological chaperones (PCs) represents a promising new therapeutic strategy for the treatment of rare genetic disorders associated with protein misfolding.… (more)

Subjects/Keywords: Pharamacological Chaperones; Genetic Disorders

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APA (6th Edition):

Shanmuganathan, M. (2015). High-Quality Screening of Pharmacological Chaperones for Enzyme Enhancement Therapy. (Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/16733

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):

Shanmuganathan, Meera. “High-Quality Screening of Pharmacological Chaperones for Enzyme Enhancement Therapy.” 2015. Thesis, McMaster University. Accessed January 19, 2021. http://hdl.handle.net/11375/16733.

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

MLA Handbook (7th Edition):

Shanmuganathan, Meera. “High-Quality Screening of Pharmacological Chaperones for Enzyme Enhancement Therapy.” 2015. Web. 19 Jan 2021.

Vancouver:

Shanmuganathan M. High-Quality Screening of Pharmacological Chaperones for Enzyme Enhancement Therapy. [Internet] [Thesis]. McMaster University; 2015. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/11375/16733.

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

Council of Science Editors:

Shanmuganathan M. High-Quality Screening of Pharmacological Chaperones for Enzyme Enhancement Therapy. [Thesis]. McMaster University; 2015. Available from: http://hdl.handle.net/11375/16733

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


University of Otago

4. Rogawski, David. Biophysical Study of the Molecular Chaperone DnaK by Intramolecular FRET .

Degree: 2010, University of Otago

 DnaK is a 70 kilodalton heat shock protein and molecular chaperone from Escherichia coli with an N-terminal nucleotide binding domain and C-terminal substrate binding domain.… (more)

Subjects/Keywords: Hsp70; Molecular chaperones; DnaK; FRET

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APA (6th Edition):

Rogawski, D. (2010). Biophysical Study of the Molecular Chaperone DnaK by Intramolecular FRET . (Masters Thesis). University of Otago. Retrieved from http://hdl.handle.net/10523/391

Chicago Manual of Style (16th Edition):

Rogawski, David. “Biophysical Study of the Molecular Chaperone DnaK by Intramolecular FRET .” 2010. Masters Thesis, University of Otago. Accessed January 19, 2021. http://hdl.handle.net/10523/391.

MLA Handbook (7th Edition):

Rogawski, David. “Biophysical Study of the Molecular Chaperone DnaK by Intramolecular FRET .” 2010. Web. 19 Jan 2021.

Vancouver:

Rogawski D. Biophysical Study of the Molecular Chaperone DnaK by Intramolecular FRET . [Internet] [Masters thesis]. University of Otago; 2010. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/10523/391.

Council of Science Editors:

Rogawski D. Biophysical Study of the Molecular Chaperone DnaK by Intramolecular FRET . [Masters Thesis]. University of Otago; 2010. Available from: http://hdl.handle.net/10523/391


University of Texas Medical Branch – Galveston

5. [No author]. The UNC-45 molecular chaperone: Its interactions with myosin and its thermosensing properties .

Degree: University of Texas Medical Branch – Galveston

 In order to perform their biological functions, proteins must fold into a defined structure which is termed the “native state”. In some cases proteins can… (more)

Subjects/Keywords: Chaperones; Myosin

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APA (6th Edition):

author], [. (n.d.). The UNC-45 molecular chaperone: Its interactions with myosin and its thermosensing properties . (Thesis). University of Texas Medical Branch – Galveston. Retrieved from http://hdl.handle.net/2152.3/739

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

author], [No. “The UNC-45 molecular chaperone: Its interactions with myosin and its thermosensing properties .” Thesis, University of Texas Medical Branch – Galveston. Accessed January 19, 2021. http://hdl.handle.net/2152.3/739.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

author], [No. “The UNC-45 molecular chaperone: Its interactions with myosin and its thermosensing properties .” Web. 19 Jan 2021.

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

Vancouver:

author] [. The UNC-45 molecular chaperone: Its interactions with myosin and its thermosensing properties . [Internet] [Thesis]. University of Texas Medical Branch – Galveston; [cited 2021 Jan 19]. Available from: http://hdl.handle.net/2152.3/739.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

author] [. The UNC-45 molecular chaperone: Its interactions with myosin and its thermosensing properties . [Thesis]. University of Texas Medical Branch – Galveston; Available from: http://hdl.handle.net/2152.3/739

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


University of the Western Cape

6. Kimar, Charlene Patricia. Deciphering a potential cytoprotective role of novel heat shock responsive proteins using a proteomic approach .

Degree: 2011, University of the Western Cape

 Myocardial infarction, commonly known as a heart attack, is a condition where the blood supply to the heart tissue is cut off, starving the tissue… (more)

Subjects/Keywords: Cardiomyocytes; Apoptosis; Molecular chaperones

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APA (6th Edition):

Kimar, C. P. (2011). Deciphering a potential cytoprotective role of novel heat shock responsive proteins using a proteomic approach . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/4232

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):

Kimar, Charlene Patricia. “Deciphering a potential cytoprotective role of novel heat shock responsive proteins using a proteomic approach .” 2011. Thesis, University of the Western Cape. Accessed January 19, 2021. http://hdl.handle.net/11394/4232.

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

MLA Handbook (7th Edition):

Kimar, Charlene Patricia. “Deciphering a potential cytoprotective role of novel heat shock responsive proteins using a proteomic approach .” 2011. Web. 19 Jan 2021.

Vancouver:

Kimar CP. Deciphering a potential cytoprotective role of novel heat shock responsive proteins using a proteomic approach . [Internet] [Thesis]. University of the Western Cape; 2011. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/11394/4232.

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

Council of Science Editors:

Kimar CP. Deciphering a potential cytoprotective role of novel heat shock responsive proteins using a proteomic approach . [Thesis]. University of the Western Cape; 2011. Available from: http://hdl.handle.net/11394/4232

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

7. Stein, Kevin. Yeast Prion Variants as Models of the Phenotypic and Pathological Consequences of Amyloid Polymorphism.

Degree: PhD, Biology and Biomedical Sciences: Molecular Cell Biology, 2014, Washington University in St. Louis

  Protein aggregation is the hallmark of protein conformational disorders such as Alzheimer's disease and prion diseases. Prions are infectious proteins that propagate a self-… (more)

Subjects/Keywords: chaperones; prion strains; [RNQ+]; yeast

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APA (6th Edition):

Stein, K. (2014). Yeast Prion Variants as Models of the Phenotypic and Pathological Consequences of Amyloid Polymorphism. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/etd/1350

Chicago Manual of Style (16th Edition):

Stein, Kevin. “Yeast Prion Variants as Models of the Phenotypic and Pathological Consequences of Amyloid Polymorphism.” 2014. Doctoral Dissertation, Washington University in St. Louis. Accessed January 19, 2021. https://openscholarship.wustl.edu/etd/1350.

MLA Handbook (7th Edition):

Stein, Kevin. “Yeast Prion Variants as Models of the Phenotypic and Pathological Consequences of Amyloid Polymorphism.” 2014. Web. 19 Jan 2021.

Vancouver:

Stein K. Yeast Prion Variants as Models of the Phenotypic and Pathological Consequences of Amyloid Polymorphism. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2014. [cited 2021 Jan 19]. Available from: https://openscholarship.wustl.edu/etd/1350.

Council of Science Editors:

Stein K. Yeast Prion Variants as Models of the Phenotypic and Pathological Consequences of Amyloid Polymorphism. [Doctoral Dissertation]. Washington University in St. Louis; 2014. Available from: https://openscholarship.wustl.edu/etd/1350


University of South Florida

8. Blair, Laura J. Age-associated increases in FKBP51 facilitate tau neurotoxicity.

Degree: 2014, University of South Florida

 Tau is a protein which regulates microtubule stability and is heavily involved in axonal transport. This stability is dynamically controlled in part by over 40… (more)

Subjects/Keywords: chaperones; FKBP5; Hsp90; oligomers; Neurosciences

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APA (6th Edition):

Blair, L. J. (2014). Age-associated increases in FKBP51 facilitate tau neurotoxicity. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/5185

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):

Blair, Laura J. “Age-associated increases in FKBP51 facilitate tau neurotoxicity.” 2014. Thesis, University of South Florida. Accessed January 19, 2021. https://scholarcommons.usf.edu/etd/5185.

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

MLA Handbook (7th Edition):

Blair, Laura J. “Age-associated increases in FKBP51 facilitate tau neurotoxicity.” 2014. Web. 19 Jan 2021.

Vancouver:

Blair LJ. Age-associated increases in FKBP51 facilitate tau neurotoxicity. [Internet] [Thesis]. University of South Florida; 2014. [cited 2021 Jan 19]. Available from: https://scholarcommons.usf.edu/etd/5185.

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

Council of Science Editors:

Blair LJ. Age-associated increases in FKBP51 facilitate tau neurotoxicity. [Thesis]. University of South Florida; 2014. Available from: https://scholarcommons.usf.edu/etd/5185

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


University of Utah

9. Stadtmueller, Beth Marie. Structural studies of proteasome assembly chaperones and activator complexes.

Degree: PhD, Biochemistry, 2010, University of Utah

 This dissertation describes structural and biochemical studies on proteasome assembly chaperones and proteasome activator complexes. Chapters 1 and 2 provide a detailed introduction to proteasome… (more)

Subjects/Keywords: Proteasome; Structural biology; Assembly chaperones; Activator complexes

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APA (6th Edition):

Stadtmueller, B. M. (2010). Structural studies of proteasome assembly chaperones and activator complexes. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/582/rec/2283

Chicago Manual of Style (16th Edition):

Stadtmueller, Beth Marie. “Structural studies of proteasome assembly chaperones and activator complexes.” 2010. Doctoral Dissertation, University of Utah. Accessed January 19, 2021. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/582/rec/2283.

MLA Handbook (7th Edition):

Stadtmueller, Beth Marie. “Structural studies of proteasome assembly chaperones and activator complexes.” 2010. Web. 19 Jan 2021.

Vancouver:

Stadtmueller BM. Structural studies of proteasome assembly chaperones and activator complexes. [Internet] [Doctoral dissertation]. University of Utah; 2010. [cited 2021 Jan 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/582/rec/2283.

Council of Science Editors:

Stadtmueller BM. Structural studies of proteasome assembly chaperones and activator complexes. [Doctoral Dissertation]. University of Utah; 2010. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/582/rec/2283


Texas A&M University

10. Shoup, Daniel Wayne. The Impact Of Hidden Aggregate Structure On Molecular Chaperone Disaggregation Revealed By Single Particle Fluorescence Burst Analysis.

Degree: PhD, Biochemistry, 2016, Texas A&M University

 Molecular chaperones are tasked with folding and disassembling the misfolded and aggregated non-native proteins that arise during biosynthesis or upon environmental stress. However, the heterogeneous… (more)

Subjects/Keywords: protein folding; protein aggregation; chaperones; Disaggregation

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APA (6th Edition):

Shoup, D. W. (2016). The Impact Of Hidden Aggregate Structure On Molecular Chaperone Disaggregation Revealed By Single Particle Fluorescence Burst Analysis. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/157112

Chicago Manual of Style (16th Edition):

Shoup, Daniel Wayne. “The Impact Of Hidden Aggregate Structure On Molecular Chaperone Disaggregation Revealed By Single Particle Fluorescence Burst Analysis.” 2016. Doctoral Dissertation, Texas A&M University. Accessed January 19, 2021. http://hdl.handle.net/1969.1/157112.

MLA Handbook (7th Edition):

Shoup, Daniel Wayne. “The Impact Of Hidden Aggregate Structure On Molecular Chaperone Disaggregation Revealed By Single Particle Fluorescence Burst Analysis.” 2016. Web. 19 Jan 2021.

Vancouver:

Shoup DW. The Impact Of Hidden Aggregate Structure On Molecular Chaperone Disaggregation Revealed By Single Particle Fluorescence Burst Analysis. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1969.1/157112.

Council of Science Editors:

Shoup DW. The Impact Of Hidden Aggregate Structure On Molecular Chaperone Disaggregation Revealed By Single Particle Fluorescence Burst Analysis. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/157112


University of Toronto

11. Friesen, Erik Loewen. Characterizing the Bcl-2 Associated Athanogene 5 Interactome in the Context of Parkinson’s Disease.

Degree: 2018, University of Toronto

Aberrant alpha-synuclein aggregation is associated with the onset and progression of Parkinson’s disease (PD). This has made molecular chaperones, a class of proteins responsible for… (more)

Subjects/Keywords: BAG5; Chaperones; p62; Parkinson's disease; Proteomics; 0317

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APA (6th Edition):

Friesen, E. L. (2018). Characterizing the Bcl-2 Associated Athanogene 5 Interactome in the Context of Parkinson’s Disease. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/101587

Chicago Manual of Style (16th Edition):

Friesen, Erik Loewen. “Characterizing the Bcl-2 Associated Athanogene 5 Interactome in the Context of Parkinson’s Disease.” 2018. Masters Thesis, University of Toronto. Accessed January 19, 2021. http://hdl.handle.net/1807/101587.

MLA Handbook (7th Edition):

Friesen, Erik Loewen. “Characterizing the Bcl-2 Associated Athanogene 5 Interactome in the Context of Parkinson’s Disease.” 2018. Web. 19 Jan 2021.

Vancouver:

Friesen EL. Characterizing the Bcl-2 Associated Athanogene 5 Interactome in the Context of Parkinson’s Disease. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1807/101587.

Council of Science Editors:

Friesen EL. Characterizing the Bcl-2 Associated Athanogene 5 Interactome in the Context of Parkinson’s Disease. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/101587


University of Victoria

12. Savic, Neda. Insights into the comparative biological roles of S. cerevisiae nucleoplasmin-like FKBPs Fpr3 and Fpr4.

Degree: Department of Biochemistry and Microbiology, 2020, University of Victoria

 The nucleoplasmin (NPM) family of acidic histone chaperones and the FK506-binding (FKBP) peptidyl proline isomerases are both linked to chromatin regulation. In vertebrates, NPM and… (more)

Subjects/Keywords: chromatin; histone chaperones; paralog; genetic interactions; nucleolus

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APA (6th Edition):

Savic, N. (2020). Insights into the comparative biological roles of S. cerevisiae nucleoplasmin-like FKBPs Fpr3 and Fpr4. (Thesis). University of Victoria. Retrieved from http://hdl.handle.net/1828/11464

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):

Savic, Neda. “Insights into the comparative biological roles of S. cerevisiae nucleoplasmin-like FKBPs Fpr3 and Fpr4.” 2020. Thesis, University of Victoria. Accessed January 19, 2021. http://hdl.handle.net/1828/11464.

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

MLA Handbook (7th Edition):

Savic, Neda. “Insights into the comparative biological roles of S. cerevisiae nucleoplasmin-like FKBPs Fpr3 and Fpr4.” 2020. Web. 19 Jan 2021.

Vancouver:

Savic N. Insights into the comparative biological roles of S. cerevisiae nucleoplasmin-like FKBPs Fpr3 and Fpr4. [Internet] [Thesis]. University of Victoria; 2020. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1828/11464.

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

Council of Science Editors:

Savic N. Insights into the comparative biological roles of S. cerevisiae nucleoplasmin-like FKBPs Fpr3 and Fpr4. [Thesis]. University of Victoria; 2020. Available from: http://hdl.handle.net/1828/11464

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


University of Hong Kong

13. 張哲豪. Triptolide inhibits Hsp90β atpase and chaperone activity to promote cell cycle arrest and programmed cell death through multiple regulations.

Degree: 2015, University of Hong Kong

Subjects/Keywords: Triptolide; Molecular chaperones

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APA (6th Edition):

張哲豪. (2015). Triptolide inhibits Hsp90β atpase and chaperone activity to promote cell cycle arrest and programmed cell death through multiple regulations. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/209519

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

Chicago Manual of Style (16th Edition):

張哲豪. “Triptolide inhibits Hsp90β atpase and chaperone activity to promote cell cycle arrest and programmed cell death through multiple regulations.” 2015. Thesis, University of Hong Kong. Accessed January 19, 2021. http://hdl.handle.net/10722/209519.

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

MLA Handbook (7th Edition):

張哲豪. “Triptolide inhibits Hsp90β atpase and chaperone activity to promote cell cycle arrest and programmed cell death through multiple regulations.” 2015. Web. 19 Jan 2021.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

張哲豪. Triptolide inhibits Hsp90β atpase and chaperone activity to promote cell cycle arrest and programmed cell death through multiple regulations. [Internet] [Thesis]. University of Hong Kong; 2015. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/10722/209519.

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

Council of Science Editors:

張哲豪. Triptolide inhibits Hsp90β atpase and chaperone activity to promote cell cycle arrest and programmed cell death through multiple regulations. [Thesis]. University of Hong Kong; 2015. Available from: http://hdl.handle.net/10722/209519

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


University of Hong Kong

14. Zhang, Zhehao. Triptolide inhibits Hsp90β atpase and chaperone activity to promote cell cycle arrest and programmed cell death through multiple regulations.

Degree: 2015, University of Hong Kong

 Triptolide (TL) is a potent antitumor, anti-inflammatory and immunosuppressive compound extracted from Thunder God vine (Tripeterygium wilfordii Hook f.), which is traditionally used in Chinese… (more)

Subjects/Keywords: Triptolide; Molecular chaperones

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APA (6th Edition):

Zhang, Z. (2015). Triptolide inhibits Hsp90β atpase and chaperone activity to promote cell cycle arrest and programmed cell death through multiple regulations. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/222914

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):

Zhang, Zhehao. “Triptolide inhibits Hsp90β atpase and chaperone activity to promote cell cycle arrest and programmed cell death through multiple regulations.” 2015. Thesis, University of Hong Kong. Accessed January 19, 2021. http://hdl.handle.net/10722/222914.

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

MLA Handbook (7th Edition):

Zhang, Zhehao. “Triptolide inhibits Hsp90β atpase and chaperone activity to promote cell cycle arrest and programmed cell death through multiple regulations.” 2015. Web. 19 Jan 2021.

Vancouver:

Zhang Z. Triptolide inhibits Hsp90β atpase and chaperone activity to promote cell cycle arrest and programmed cell death through multiple regulations. [Internet] [Thesis]. University of Hong Kong; 2015. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/10722/222914.

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

Council of Science Editors:

Zhang Z. Triptolide inhibits Hsp90β atpase and chaperone activity to promote cell cycle arrest and programmed cell death through multiple regulations. [Thesis]. University of Hong Kong; 2015. Available from: http://hdl.handle.net/10722/222914

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


Georgia Tech

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

Degree: MS, Biology, 2005, Georgia Tech

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

Subjects/Keywords: Ubiquitin; Proteasome; Chaperones

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Tennant, Esther Paula. “Interactions of the chaperones and components of UB system in the formation and propagation of the yeast prion [PSI+].” 2005. Masters Thesis, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/7157.

MLA Handbook (7th Edition):

Tennant, Esther Paula. “Interactions of the chaperones and components of UB system in the formation and propagation of the yeast prion [PSI+].” 2005. Web. 19 Jan 2021.

Vancouver:

Tennant EP. Interactions of the chaperones and components of UB system in the formation and propagation of the yeast prion [PSI+]. [Internet] [Masters thesis]. Georgia Tech; 2005. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/7157.

Council of Science Editors:

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

16. De La Mota-Peynado, Alina M. The role of the proteasome-associated protein Ecm29 in quality control of the proteasome.

Degree: PhD, Division of Biology, 2014, Kansas State University

 The ubiquitin-proteasome pathway is the major pathway of selective protein degradation in the cell. Disruption of this pathway affects cellular protein homeostasis and contributes to… (more)

Subjects/Keywords: Proteasome assembly; Ecm29; Molecular chaperones; Biology (0306)

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APA (6th Edition):

De La Mota-Peynado, A. M. (2014). The role of the proteasome-associated protein Ecm29 in quality control of the proteasome. (Doctoral Dissertation). Kansas State University. Retrieved from http://hdl.handle.net/2097/18200

Chicago Manual of Style (16th Edition):

De La Mota-Peynado, Alina M. “The role of the proteasome-associated protein Ecm29 in quality control of the proteasome.” 2014. Doctoral Dissertation, Kansas State University. Accessed January 19, 2021. http://hdl.handle.net/2097/18200.

MLA Handbook (7th Edition):

De La Mota-Peynado, Alina M. “The role of the proteasome-associated protein Ecm29 in quality control of the proteasome.” 2014. Web. 19 Jan 2021.

Vancouver:

De La Mota-Peynado AM. The role of the proteasome-associated protein Ecm29 in quality control of the proteasome. [Internet] [Doctoral dissertation]. Kansas State University; 2014. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/2097/18200.

Council of Science Editors:

De La Mota-Peynado AM. The role of the proteasome-associated protein Ecm29 in quality control of the proteasome. [Doctoral Dissertation]. Kansas State University; 2014. Available from: http://hdl.handle.net/2097/18200


Universidad de Chile

17. Toro Pávez, Barbra Deborah. Inhibición de la autofagia mediada por chaperonas genera sobreactivación de macroautofagia y sobrevida en cardiomiocitos expuestos a estrés nutricional.

Degree: 2014, Universidad de Chile

 El catabolismo de proteínas es un proceso celular fundamental que ha captado la atención de distintos investigadores en los últimos años. Existen dos mecanismos por… (more)

Subjects/Keywords: Autofagia; Chaperones moleculares; Células del corazón

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APA (6th Edition):

Toro Pávez, B. D. (2014). Inhibición de la autofagia mediada por chaperonas genera sobreactivación de macroautofagia y sobrevida en cardiomiocitos expuestos a estrés nutricional. (Thesis). Universidad de Chile. Retrieved from http://repositorio.uchile.cl/handle/2250/116885

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):

Toro Pávez, Barbra Deborah. “Inhibición de la autofagia mediada por chaperonas genera sobreactivación de macroautofagia y sobrevida en cardiomiocitos expuestos a estrés nutricional.” 2014. Thesis, Universidad de Chile. Accessed January 19, 2021. http://repositorio.uchile.cl/handle/2250/116885.

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

MLA Handbook (7th Edition):

Toro Pávez, Barbra Deborah. “Inhibición de la autofagia mediada por chaperonas genera sobreactivación de macroautofagia y sobrevida en cardiomiocitos expuestos a estrés nutricional.” 2014. Web. 19 Jan 2021.

Vancouver:

Toro Pávez BD. Inhibición de la autofagia mediada por chaperonas genera sobreactivación de macroautofagia y sobrevida en cardiomiocitos expuestos a estrés nutricional. [Internet] [Thesis]. Universidad de Chile; 2014. [cited 2021 Jan 19]. Available from: http://repositorio.uchile.cl/handle/2250/116885.

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

Council of Science Editors:

Toro Pávez BD. Inhibición de la autofagia mediada por chaperonas genera sobreactivación de macroautofagia y sobrevida en cardiomiocitos expuestos a estrés nutricional. [Thesis]. Universidad de Chile; 2014. Available from: http://repositorio.uchile.cl/handle/2250/116885

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


University of Louisville

18. Brinkworth, Amanda J. Identification and biochemical characterization of the CHLAMYDIA TRACHOMATIS type III secretion chaperone, SLC1, and its role in the translocation of the invasion-associated effector TARP.

Degree: PhD, 2011, University of Louisville

 Chlamydia trachomatis is an obligate intracellular pathogen that utilizes a type III secretion system to enter mammalian cells and establish an intracellular niche. TARP, the… (more)

Subjects/Keywords: Chaperones; Secretion; Microbiology; Chlamydia; Type III; TARP

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APA (6th Edition):

Brinkworth, A. J. (2011). Identification and biochemical characterization of the CHLAMYDIA TRACHOMATIS type III secretion chaperone, SLC1, and its role in the translocation of the invasion-associated effector TARP. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/153 ; https://ir.library.louisville.edu/etd/153

Chicago Manual of Style (16th Edition):

Brinkworth, Amanda J. “Identification and biochemical characterization of the CHLAMYDIA TRACHOMATIS type III secretion chaperone, SLC1, and its role in the translocation of the invasion-associated effector TARP.” 2011. Doctoral Dissertation, University of Louisville. Accessed January 19, 2021. 10.18297/etd/153 ; https://ir.library.louisville.edu/etd/153.

MLA Handbook (7th Edition):

Brinkworth, Amanda J. “Identification and biochemical characterization of the CHLAMYDIA TRACHOMATIS type III secretion chaperone, SLC1, and its role in the translocation of the invasion-associated effector TARP.” 2011. Web. 19 Jan 2021.

Vancouver:

Brinkworth AJ. Identification and biochemical characterization of the CHLAMYDIA TRACHOMATIS type III secretion chaperone, SLC1, and its role in the translocation of the invasion-associated effector TARP. [Internet] [Doctoral dissertation]. University of Louisville; 2011. [cited 2021 Jan 19]. Available from: 10.18297/etd/153 ; https://ir.library.louisville.edu/etd/153.

Council of Science Editors:

Brinkworth AJ. Identification and biochemical characterization of the CHLAMYDIA TRACHOMATIS type III secretion chaperone, SLC1, and its role in the translocation of the invasion-associated effector TARP. [Doctoral Dissertation]. University of Louisville; 2011. Available from: 10.18297/etd/153 ; https://ir.library.louisville.edu/etd/153


University of Sydney

19. Green, Bradley. Matrix metalloproteinase binding agents for luminescence and radioimaging of metastatic tumours .

Degree: 2013, University of Sydney

 Matrix metalloproteinases (MMPs) are zinc-based endopeptidases responsible for the degradation and remodelling of the extracellular matrix in normal growth and wound healing. MMP expression and… (more)

Subjects/Keywords: Matrix metalloproteinase; Radioimaging; Cobalt(III) chaperones

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APA (6th Edition):

Green, B. (2013). Matrix metalloproteinase binding agents for luminescence and radioimaging of metastatic tumours . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/10095

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):

Green, Bradley. “Matrix metalloproteinase binding agents for luminescence and radioimaging of metastatic tumours .” 2013. Thesis, University of Sydney. Accessed January 19, 2021. http://hdl.handle.net/2123/10095.

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

MLA Handbook (7th Edition):

Green, Bradley. “Matrix metalloproteinase binding agents for luminescence and radioimaging of metastatic tumours .” 2013. Web. 19 Jan 2021.

Vancouver:

Green B. Matrix metalloproteinase binding agents for luminescence and radioimaging of metastatic tumours . [Internet] [Thesis]. University of Sydney; 2013. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/2123/10095.

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

Council of Science Editors:

Green B. Matrix metalloproteinase binding agents for luminescence and radioimaging of metastatic tumours . [Thesis]. University of Sydney; 2013. Available from: http://hdl.handle.net/2123/10095

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


University of New South Wales

20. Bowden, Quill. Utilising fluorescence microscopy to visualise the dynamics and interactions of molecular chaperones and α-Synuclein.

Degree: Centre for Vascular Research, 2016, University of New South Wales

 In Parkinson’s Disease (PD), the protein α-synuclein and its early stage oligomers have been implicated as the primary cause of neuronal toxicity. Molecular chaperones play… (more)

Subjects/Keywords: Molecular Chaperones; Microscopy; α-Synuclein; Fluorescence

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APA (6th Edition):

Bowden, Q. (2016). Utilising fluorescence microscopy to visualise the dynamics and interactions of molecular chaperones and α-Synuclein. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/57211 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42851/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Bowden, Quill. “Utilising fluorescence microscopy to visualise the dynamics and interactions of molecular chaperones and α-Synuclein.” 2016. Doctoral Dissertation, University of New South Wales. Accessed January 19, 2021. http://handle.unsw.edu.au/1959.4/57211 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42851/SOURCE02?view=true.

MLA Handbook (7th Edition):

Bowden, Quill. “Utilising fluorescence microscopy to visualise the dynamics and interactions of molecular chaperones and α-Synuclein.” 2016. Web. 19 Jan 2021.

Vancouver:

Bowden Q. Utilising fluorescence microscopy to visualise the dynamics and interactions of molecular chaperones and α-Synuclein. [Internet] [Doctoral dissertation]. University of New South Wales; 2016. [cited 2021 Jan 19]. Available from: http://handle.unsw.edu.au/1959.4/57211 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42851/SOURCE02?view=true.

Council of Science Editors:

Bowden Q. Utilising fluorescence microscopy to visualise the dynamics and interactions of molecular chaperones and α-Synuclein. [Doctoral Dissertation]. University of New South Wales; 2016. Available from: http://handle.unsw.edu.au/1959.4/57211 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42851/SOURCE02?view=true

21. Cardeal, Isabel Cristina Mendonça de Azevedo. Uso terapêutico de chaperones em doenças conformacionais.

Degree: 2013, Universidade Fernando Pessoa

Projeto de Pós-Graduação/Dissertação apresentado à Universidade Fernando Pessoa como parte dos requisitos para obtenção do grau de Mestre em Ciências Farmacêuticas

Os chaperones são proteínas… (more)

Subjects/Keywords: Chaperones; Misfolding; Lisossoma; Proteassoma; Doenças conformacionais; Chaperones; Misfolding; Lysosome; Proteasome; Conformational diseases

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APA (6th Edition):

Cardeal, I. C. M. d. A. (2013). Uso terapêutico de chaperones em doenças conformacionais. (Thesis). Universidade Fernando Pessoa. Retrieved from https://www.rcaap.pt/detail.jsp?id=oai:bdigital.ufp.pt:10284/4093

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):

Cardeal, Isabel Cristina Mendonça de Azevedo. “Uso terapêutico de chaperones em doenças conformacionais.” 2013. Thesis, Universidade Fernando Pessoa. Accessed January 19, 2021. https://www.rcaap.pt/detail.jsp?id=oai:bdigital.ufp.pt:10284/4093.

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

MLA Handbook (7th Edition):

Cardeal, Isabel Cristina Mendonça de Azevedo. “Uso terapêutico de chaperones em doenças conformacionais.” 2013. Web. 19 Jan 2021.

Vancouver:

Cardeal ICMdA. Uso terapêutico de chaperones em doenças conformacionais. [Internet] [Thesis]. Universidade Fernando Pessoa; 2013. [cited 2021 Jan 19]. Available from: https://www.rcaap.pt/detail.jsp?id=oai:bdigital.ufp.pt:10284/4093.

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

Council of Science Editors:

Cardeal ICMdA. Uso terapêutico de chaperones em doenças conformacionais. [Thesis]. Universidade Fernando Pessoa; 2013. Available from: https://www.rcaap.pt/detail.jsp?id=oai:bdigital.ufp.pt:10284/4093

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


Georgia Tech

22. Gokhale, Kavita Chandan. Interactions between endogenous prions, chaperones and polyglutamine proteins in the yeast model.

Degree: PhD, Biology, 2005, Georgia Tech

 Poly-Q expanded exon 1 of huntingtin (Q103) fused to GFP is toxic to yeast cells containing endogenous yeast prions, [PIN+] ([RNQ+]) and/or [PSI+], which presumably… (more)

Subjects/Keywords: Chaperones; Glutamine; Molecular chaperones; Prions; Yeast

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

APA (6th Edition):

Gokhale, K. C. (2005). Interactions between endogenous prions, chaperones and polyglutamine proteins in the yeast model. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/6856

Chicago Manual of Style (16th Edition):

Gokhale, Kavita Chandan. “Interactions between endogenous prions, chaperones and polyglutamine proteins in the yeast model.” 2005. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2021. http://hdl.handle.net/1853/6856.

MLA Handbook (7th Edition):

Gokhale, Kavita Chandan. “Interactions between endogenous prions, chaperones and polyglutamine proteins in the yeast model.” 2005. Web. 19 Jan 2021.

Vancouver:

Gokhale KC. Interactions between endogenous prions, chaperones and polyglutamine proteins in the yeast model. [Internet] [Doctoral dissertation]. Georgia Tech; 2005. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1853/6856.

Council of Science Editors:

Gokhale KC. Interactions between endogenous prions, chaperones and polyglutamine proteins in the yeast model. [Doctoral Dissertation]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/6856


Johannes Gutenberg Universität Mainz

23. Schönbühler, Bianca. Die Regulation der Ubiquitinligase CHIP durch das Cochaperon BAG2 im zellulären System und im Kontext der replikativen Seneszenz.

Degree: 2014, Johannes Gutenberg Universität Mainz

 Eine funktionierende Proteinqualitätskontrolle ist essenziell für die Vitalität einer Zelle. Das dynamische Gleichgewicht zwischen Proteinfaltung und -degradation wird von molekularen Chaperonen aufrechterhalten, deren Aktivität wiederum… (more)

Subjects/Keywords: Proteinqualitätskontrolle; Chaperone; Cochaperone; Proteinabbau; Alterung; Protein quality control; chaperones, co-chaperones; protein degradation; aging; Life sciences

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APA (6th Edition):

Schönbühler, B. (2014). Die Regulation der Ubiquitinligase CHIP durch das Cochaperon BAG2 im zellulären System und im Kontext der replikativen Seneszenz. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2014/3829/

Chicago Manual of Style (16th Edition):

Schönbühler, Bianca. “Die Regulation der Ubiquitinligase CHIP durch das Cochaperon BAG2 im zellulären System und im Kontext der replikativen Seneszenz.” 2014. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed January 19, 2021. http://ubm.opus.hbz-nrw.de/volltexte/2014/3829/.

MLA Handbook (7th Edition):

Schönbühler, Bianca. “Die Regulation der Ubiquitinligase CHIP durch das Cochaperon BAG2 im zellulären System und im Kontext der replikativen Seneszenz.” 2014. Web. 19 Jan 2021.

Vancouver:

Schönbühler B. Die Regulation der Ubiquitinligase CHIP durch das Cochaperon BAG2 im zellulären System und im Kontext der replikativen Seneszenz. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2014. [cited 2021 Jan 19]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2014/3829/.

Council of Science Editors:

Schönbühler B. Die Regulation der Ubiquitinligase CHIP durch das Cochaperon BAG2 im zellulären System und im Kontext der replikativen Seneszenz. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2014. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2014/3829/


University of Edinburgh

24. Ahl, Alexander. Drosophila Ttc12 genes are putative co-chaperones for dynein assembly and docking in motile cilia.

Degree: PhD, 2020, University of Edinburgh

 Motile cilia have many developmental and physiological functions. The hallmark of motile cilia are their axonemal dynein motor proteins that generate movement. These large protein… (more)

Subjects/Keywords: cilia; ciliopathies; dynein; DNAAFs; assembly factors; chaperones; co-chaperones; drosophila melanogaster; sperm; chordotonal neurons; TTC12; TPR

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APA (6th Edition):

Ahl, A. (2020). Drosophila Ttc12 genes are putative co-chaperones for dynein assembly and docking in motile cilia. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/36848

Chicago Manual of Style (16th Edition):

Ahl, Alexander. “Drosophila Ttc12 genes are putative co-chaperones for dynein assembly and docking in motile cilia.” 2020. Doctoral Dissertation, University of Edinburgh. Accessed January 19, 2021. http://hdl.handle.net/1842/36848.

MLA Handbook (7th Edition):

Ahl, Alexander. “Drosophila Ttc12 genes are putative co-chaperones for dynein assembly and docking in motile cilia.” 2020. Web. 19 Jan 2021.

Vancouver:

Ahl A. Drosophila Ttc12 genes are putative co-chaperones for dynein assembly and docking in motile cilia. [Internet] [Doctoral dissertation]. University of Edinburgh; 2020. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1842/36848.

Council of Science Editors:

Ahl A. Drosophila Ttc12 genes are putative co-chaperones for dynein assembly and docking in motile cilia. [Doctoral Dissertation]. University of Edinburgh; 2020. Available from: http://hdl.handle.net/1842/36848


University of Edinburgh

25. Ahl, Alexander. Drosophila Ttc12 genes are putative co-chaperones for dynein assembly and docking in motile cilia.

Degree: PhD, 2020, University of Edinburgh

 Motile cilia have many developmental and physiological functions. The hallmark of motile cilia are their axonemal dynein motor proteins that generate movement. These large protein… (more)

Subjects/Keywords: cilia; ciliopathies; dynein; DNAAFs; assembly factors; chaperones; co-chaperones; drosophila melanogaster; sperm; chordotonal neurons; TTC12; TPR

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APA (6th Edition):

Ahl, A. (2020). Drosophila Ttc12 genes are putative co-chaperones for dynein assembly and docking in motile cilia. (Doctoral Dissertation). University of Edinburgh. Retrieved from https://doi.org/10.7488/era/150 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.802333

Chicago Manual of Style (16th Edition):

Ahl, Alexander. “Drosophila Ttc12 genes are putative co-chaperones for dynein assembly and docking in motile cilia.” 2020. Doctoral Dissertation, University of Edinburgh. Accessed January 19, 2021. https://doi.org/10.7488/era/150 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.802333.

MLA Handbook (7th Edition):

Ahl, Alexander. “Drosophila Ttc12 genes are putative co-chaperones for dynein assembly and docking in motile cilia.” 2020. Web. 19 Jan 2021.

Vancouver:

Ahl A. Drosophila Ttc12 genes are putative co-chaperones for dynein assembly and docking in motile cilia. [Internet] [Doctoral dissertation]. University of Edinburgh; 2020. [cited 2021 Jan 19]. Available from: https://doi.org/10.7488/era/150 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.802333.

Council of Science Editors:

Ahl A. Drosophila Ttc12 genes are putative co-chaperones for dynein assembly and docking in motile cilia. [Doctoral Dissertation]. University of Edinburgh; 2020. Available from: https://doi.org/10.7488/era/150 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.802333


NSYSU

26. Hsiao, Po-Lun. The roles of androgen receptor aggregates in embryonic stem cell differentiation.

Degree: Master, Biological Sciences, 2012, NSYSU

 Androgen receptor (AR) is a member of the steroid hormone receptor family of molecules, and expansion of a CAG repeat encoding polyglutamine (poly-Q) in AR… (more)

Subjects/Keywords: embryonic stem cell; AR; chaperones; ER stress; AR aggregates

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APA (6th Edition):

Hsiao, P. (2012). The roles of androgen receptor aggregates in embryonic stem cell differentiation. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0215112-152652

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):

Hsiao, Po-Lun. “The roles of androgen receptor aggregates in embryonic stem cell differentiation.” 2012. Thesis, NSYSU. Accessed January 19, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0215112-152652.

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

MLA Handbook (7th Edition):

Hsiao, Po-Lun. “The roles of androgen receptor aggregates in embryonic stem cell differentiation.” 2012. Web. 19 Jan 2021.

Vancouver:

Hsiao P. The roles of androgen receptor aggregates in embryonic stem cell differentiation. [Internet] [Thesis]. NSYSU; 2012. [cited 2021 Jan 19]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0215112-152652.

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

Council of Science Editors:

Hsiao P. The roles of androgen receptor aggregates in embryonic stem cell differentiation. [Thesis]. NSYSU; 2012. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0215112-152652

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

27. Silva, Paulo Roberto das Dores da. Estudos da chaperona molecular Hsp70 mitocondrial humana - mortalina: elucidando aspectos estruturais e funcionais.

Degree: PhD, Química Orgânica e Biológica, 2015, University of São Paulo

A Hsp70 mitocondrial humana (mtHsp70 ou mortalina) está envolvida em diversos processos celulares: na matriz mitocondrial atua na importação de proteínas produzidas no citoplasma; no… (more)

Subjects/Keywords: chapernas moleculares; Hsp70; Hsp70; mitochondria; mitocôndria; molecular chaperones; mortalin; mortalina

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APA (6th Edition):

Silva, P. R. d. D. d. (2015). Estudos da chaperona molecular Hsp70 mitocondrial humana - mortalina: elucidando aspectos estruturais e funcionais. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/75/75133/tde-23062015-104546/ ;

Chicago Manual of Style (16th Edition):

Silva, Paulo Roberto das Dores da. “Estudos da chaperona molecular Hsp70 mitocondrial humana - mortalina: elucidando aspectos estruturais e funcionais.” 2015. Doctoral Dissertation, University of São Paulo. Accessed January 19, 2021. http://www.teses.usp.br/teses/disponiveis/75/75133/tde-23062015-104546/ ;.

MLA Handbook (7th Edition):

Silva, Paulo Roberto das Dores da. “Estudos da chaperona molecular Hsp70 mitocondrial humana - mortalina: elucidando aspectos estruturais e funcionais.” 2015. Web. 19 Jan 2021.

Vancouver:

Silva PRdDd. Estudos da chaperona molecular Hsp70 mitocondrial humana - mortalina: elucidando aspectos estruturais e funcionais. [Internet] [Doctoral dissertation]. University of São Paulo; 2015. [cited 2021 Jan 19]. Available from: http://www.teses.usp.br/teses/disponiveis/75/75133/tde-23062015-104546/ ;.

Council of Science Editors:

Silva PRdDd. Estudos da chaperona molecular Hsp70 mitocondrial humana - mortalina: elucidando aspectos estruturais e funcionais. [Doctoral Dissertation]. University of São Paulo; 2015. Available from: http://www.teses.usp.br/teses/disponiveis/75/75133/tde-23062015-104546/ ;


Rhodes University

28. Daniel, Sheril. Molecular characterization of the Hsp70/Hsp90 organizing protein (Hop) phosphorylation, subcellular localization and interaction with Hsp90.

Degree: Faculty of Science, Biochemistry, Microbiology and Biotechnology, 2008, Rhodes University

 Hop (Hsp70-Hsp90 Organizing Protein) is a co-chaperone of two major molecular chaperones, Hsp70 and Hsp90, and acts by transferring substrates from Hsp70 to Hsp90. Although… (more)

Subjects/Keywords: Molecular chaperones; Phosphorylation; Proteins; Heat shock proteins; Surface plasmon resonance; Cytosol

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APA (6th Edition):

Daniel, S. (2008). Molecular characterization of the Hsp70/Hsp90 organizing protein (Hop) phosphorylation, subcellular localization and interaction with Hsp90. (Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1004056

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):

Daniel, Sheril. “Molecular characterization of the Hsp70/Hsp90 organizing protein (Hop) phosphorylation, subcellular localization and interaction with Hsp90.” 2008. Thesis, Rhodes University. Accessed January 19, 2021. http://hdl.handle.net/10962/d1004056.

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

MLA Handbook (7th Edition):

Daniel, Sheril. “Molecular characterization of the Hsp70/Hsp90 organizing protein (Hop) phosphorylation, subcellular localization and interaction with Hsp90.” 2008. Web. 19 Jan 2021.

Vancouver:

Daniel S. Molecular characterization of the Hsp70/Hsp90 organizing protein (Hop) phosphorylation, subcellular localization and interaction with Hsp90. [Internet] [Thesis]. Rhodes University; 2008. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/10962/d1004056.

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

Council of Science Editors:

Daniel S. Molecular characterization of the Hsp70/Hsp90 organizing protein (Hop) phosphorylation, subcellular localization and interaction with Hsp90. [Thesis]. Rhodes University; 2008. Available from: http://hdl.handle.net/10962/d1004056

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


University of Michigan

29. Cesa, Laura. Strategies and Functional Consequences of Inhibiting Protein-Protein Interactions.

Degree: PhD, Chemical Biology, 2016, University of Michigan

 Networks of protein-protein interactions (PPIs) are essential in all aspects of cellular biology. At the nodes of these networks are multi-protein complexes that are often… (more)

Subjects/Keywords: molecular chaperones; protein-protein interactions; drug discovery; Biological Chemistry; Science

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APA (6th Edition):

Cesa, L. (2016). Strategies and Functional Consequences of Inhibiting Protein-Protein Interactions. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/135910

Chicago Manual of Style (16th Edition):

Cesa, Laura. “Strategies and Functional Consequences of Inhibiting Protein-Protein Interactions.” 2016. Doctoral Dissertation, University of Michigan. Accessed January 19, 2021. http://hdl.handle.net/2027.42/135910.

MLA Handbook (7th Edition):

Cesa, Laura. “Strategies and Functional Consequences of Inhibiting Protein-Protein Interactions.” 2016. Web. 19 Jan 2021.

Vancouver:

Cesa L. Strategies and Functional Consequences of Inhibiting Protein-Protein Interactions. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/2027.42/135910.

Council of Science Editors:

Cesa L. Strategies and Functional Consequences of Inhibiting Protein-Protein Interactions. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/135910


University of Manchester

30. Leznicki, Pawel. THE BIOGENESIS OF TAIL-ANCHORED MEMBRANE PROTEINS AT THE ENDOPLASMIC RETICULUM.

Degree: 2010, University of Manchester

 Tail anchored (TA) proteins constitute an evolutionarily-conserved group of integral membrane proteins that are characterised by the presence of a single C-terminal transmembrane segment (TMS),… (more)

Subjects/Keywords: Chaperones; Membrane integration; TRC40

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

APA (6th Edition):

Leznicki, P. (2010). THE BIOGENESIS OF TAIL-ANCHORED MEMBRANE PROTEINS AT THE ENDOPLASMIC RETICULUM. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:93922

Chicago Manual of Style (16th Edition):

Leznicki, Pawel. “THE BIOGENESIS OF TAIL-ANCHORED MEMBRANE PROTEINS AT THE ENDOPLASMIC RETICULUM.” 2010. Doctoral Dissertation, University of Manchester. Accessed January 19, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:93922.

MLA Handbook (7th Edition):

Leznicki, Pawel. “THE BIOGENESIS OF TAIL-ANCHORED MEMBRANE PROTEINS AT THE ENDOPLASMIC RETICULUM.” 2010. Web. 19 Jan 2021.

Vancouver:

Leznicki P. THE BIOGENESIS OF TAIL-ANCHORED MEMBRANE PROTEINS AT THE ENDOPLASMIC RETICULUM. [Internet] [Doctoral dissertation]. University of Manchester; 2010. [cited 2021 Jan 19]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:93922.

Council of Science Editors:

Leznicki P. THE BIOGENESIS OF TAIL-ANCHORED MEMBRANE PROTEINS AT THE ENDOPLASMIC RETICULUM. [Doctoral Dissertation]. University of Manchester; 2010. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:93922

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