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You searched for subject:(protein aggregation). Showing records 1 – 30 of 328 total matches.

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University of Waterloo

1. Primmer, Heather. Predicting and Measuring Molecular Mechanisms of Protein Aggregation.

Degree: 2011, University of Waterloo

Protein aggregation is a hallmark of a number of neurodegenerative disorders including Alzheimer’s Disease, Huntington’s Disease, and Amyotrophic Lateral Sclerosis. Despite the common occurrence of… (more)

Subjects/Keywords: protein aggregation

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

APA (6th Edition):

Primmer, H. (2011). Predicting and Measuring Molecular Mechanisms of Protein Aggregation. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/6178

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):

Primmer, Heather. “Predicting and Measuring Molecular Mechanisms of Protein Aggregation.” 2011. Thesis, University of Waterloo. Accessed January 17, 2021. http://hdl.handle.net/10012/6178.

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

MLA Handbook (7th Edition):

Primmer, Heather. “Predicting and Measuring Molecular Mechanisms of Protein Aggregation.” 2011. Web. 17 Jan 2021.

Vancouver:

Primmer H. Predicting and Measuring Molecular Mechanisms of Protein Aggregation. [Internet] [Thesis]. University of Waterloo; 2011. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/10012/6178.

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

Council of Science Editors:

Primmer H. Predicting and Measuring Molecular Mechanisms of Protein Aggregation. [Thesis]. University of Waterloo; 2011. Available from: http://hdl.handle.net/10012/6178

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


University of Miami

2. Tseng, LeinWeih Andrew. Ubiquitylation of Neuronal Pentraxin with Chromo Domain by the E3 Ubiquitin Ligase Mayven/KLHL2 and Effects on Aggresome Formation and Neuronal Cytotoxicity.

Degree: PhD, Molecular and Cellular Pharmacology (Medicine), 2010, University of Miami

  Neuronal pentraxin with chromo domain (NPCD) belongs to a family of neuronally-expressed pentraxin proteins thought to be involved in synaptic refinement and plasticity. One… (more)

Subjects/Keywords: Protein Aggregation; Neurodegeneration

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APA (6th Edition):

Tseng, L. A. (2010). Ubiquitylation of Neuronal Pentraxin with Chromo Domain by the E3 Ubiquitin Ligase Mayven/KLHL2 and Effects on Aggresome Formation and Neuronal Cytotoxicity. (Doctoral Dissertation). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_dissertations/662

Chicago Manual of Style (16th Edition):

Tseng, LeinWeih Andrew. “Ubiquitylation of Neuronal Pentraxin with Chromo Domain by the E3 Ubiquitin Ligase Mayven/KLHL2 and Effects on Aggresome Formation and Neuronal Cytotoxicity.” 2010. Doctoral Dissertation, University of Miami. Accessed January 17, 2021. https://scholarlyrepository.miami.edu/oa_dissertations/662.

MLA Handbook (7th Edition):

Tseng, LeinWeih Andrew. “Ubiquitylation of Neuronal Pentraxin with Chromo Domain by the E3 Ubiquitin Ligase Mayven/KLHL2 and Effects on Aggresome Formation and Neuronal Cytotoxicity.” 2010. Web. 17 Jan 2021.

Vancouver:

Tseng LA. Ubiquitylation of Neuronal Pentraxin with Chromo Domain by the E3 Ubiquitin Ligase Mayven/KLHL2 and Effects on Aggresome Formation and Neuronal Cytotoxicity. [Internet] [Doctoral dissertation]. University of Miami; 2010. [cited 2021 Jan 17]. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/662.

Council of Science Editors:

Tseng LA. Ubiquitylation of Neuronal Pentraxin with Chromo Domain by the E3 Ubiquitin Ligase Mayven/KLHL2 and Effects on Aggresome Formation and Neuronal Cytotoxicity. [Doctoral Dissertation]. University of Miami; 2010. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/662


University of Miami

3. Tseng, LeinWeih Andrew. Ubiquitylation of Neuronal Pentraxin with Chromo Domain by the E3 Ubiquitin Ligase Mayven/KLHL2 and Effects on Aggresome Formation and Neuronal Cytotoxicity.

Degree: PhD, Molecular and Cellular Pharmacology (Medicine), 2010, University of Miami

  Neuronal pentraxin with chromo domain (NPCD) belongs to a family of neuronally-expressed pentraxin proteins thought to be involved in synaptic refinement and plasticity. One… (more)

Subjects/Keywords: Protein Aggregation; Neurodegeneration

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APA (6th Edition):

Tseng, L. A. (2010). Ubiquitylation of Neuronal Pentraxin with Chromo Domain by the E3 Ubiquitin Ligase Mayven/KLHL2 and Effects on Aggresome Formation and Neuronal Cytotoxicity. (Doctoral Dissertation). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_dissertations/928

Chicago Manual of Style (16th Edition):

Tseng, LeinWeih Andrew. “Ubiquitylation of Neuronal Pentraxin with Chromo Domain by the E3 Ubiquitin Ligase Mayven/KLHL2 and Effects on Aggresome Formation and Neuronal Cytotoxicity.” 2010. Doctoral Dissertation, University of Miami. Accessed January 17, 2021. https://scholarlyrepository.miami.edu/oa_dissertations/928.

MLA Handbook (7th Edition):

Tseng, LeinWeih Andrew. “Ubiquitylation of Neuronal Pentraxin with Chromo Domain by the E3 Ubiquitin Ligase Mayven/KLHL2 and Effects on Aggresome Formation and Neuronal Cytotoxicity.” 2010. Web. 17 Jan 2021.

Vancouver:

Tseng LA. Ubiquitylation of Neuronal Pentraxin with Chromo Domain by the E3 Ubiquitin Ligase Mayven/KLHL2 and Effects on Aggresome Formation and Neuronal Cytotoxicity. [Internet] [Doctoral dissertation]. University of Miami; 2010. [cited 2021 Jan 17]. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/928.

Council of Science Editors:

Tseng LA. Ubiquitylation of Neuronal Pentraxin with Chromo Domain by the E3 Ubiquitin Ligase Mayven/KLHL2 and Effects on Aggresome Formation and Neuronal Cytotoxicity. [Doctoral Dissertation]. University of Miami; 2010. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/928


University of Waterloo

4. Trainor, Kyle. Inclusion Body Formation by Mutants of the Tenth Human Fibronectin Type III Domain.

Degree: 2015, University of Waterloo

 Inclusion bodies (IBs) are intracellular, insoluble protein aggregates, commonly observed when a protein of interest is expressed at high concentrations in a bacterial cell-based expression… (more)

Subjects/Keywords: protein aggregation inclusion

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APA (6th Edition):

Trainor, K. (2015). Inclusion Body Formation by Mutants of the Tenth Human Fibronectin Type III Domain. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/9239

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):

Trainor, Kyle. “Inclusion Body Formation by Mutants of the Tenth Human Fibronectin Type III Domain.” 2015. Thesis, University of Waterloo. Accessed January 17, 2021. http://hdl.handle.net/10012/9239.

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

MLA Handbook (7th Edition):

Trainor, Kyle. “Inclusion Body Formation by Mutants of the Tenth Human Fibronectin Type III Domain.” 2015. Web. 17 Jan 2021.

Vancouver:

Trainor K. Inclusion Body Formation by Mutants of the Tenth Human Fibronectin Type III Domain. [Internet] [Thesis]. University of Waterloo; 2015. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/10012/9239.

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

Council of Science Editors:

Trainor K. Inclusion Body Formation by Mutants of the Tenth Human Fibronectin Type III Domain. [Thesis]. University of Waterloo; 2015. Available from: http://hdl.handle.net/10012/9239

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


University of Manchester

5. Gilburt, James. A study of folded, denatured and aggregated states during the refolding of inclusion body proteins.

Degree: 2016, University of Manchester

 The need to high quality therapeutic proteins has grown significantly in the past 30 years. Recombinant proteins are often produced from vectors inserted into E.… (more)

Subjects/Keywords: Protein refolding; Aggregation

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

APA (6th Edition):

Gilburt, J. (2016). A study of folded, denatured and aggregated states during the refolding of inclusion body proteins. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:295840

Chicago Manual of Style (16th Edition):

Gilburt, James. “A study of folded, denatured and aggregated states during the refolding of inclusion body proteins.” 2016. Doctoral Dissertation, University of Manchester. Accessed January 17, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:295840.

MLA Handbook (7th Edition):

Gilburt, James. “A study of folded, denatured and aggregated states during the refolding of inclusion body proteins.” 2016. Web. 17 Jan 2021.

Vancouver:

Gilburt J. A study of folded, denatured and aggregated states during the refolding of inclusion body proteins. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2021 Jan 17]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:295840.

Council of Science Editors:

Gilburt J. A study of folded, denatured and aggregated states during the refolding of inclusion body proteins. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:295840


University of Texas – Austin

6. Laber, Joshua Ryan. The effects of protein-protein interactions on in vitro and in vivo behavior of protein solutions.

Degree: PhD, Chemical Engineering, 2017, University of Texas – Austin

Protein-based therapeutics such as monoclonal antibodies (mAbs) and related fragments are increasingly attractive modalities to treat a variety of diseases due to the ability to… (more)

Subjects/Keywords: Protein-protein interactions; Aggregation; Viscosity

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APA (6th Edition):

Laber, J. R. (2017). The effects of protein-protein interactions on in vitro and in vivo behavior of protein solutions. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/72727

Chicago Manual of Style (16th Edition):

Laber, Joshua Ryan. “The effects of protein-protein interactions on in vitro and in vivo behavior of protein solutions.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed January 17, 2021. http://hdl.handle.net/2152/72727.

MLA Handbook (7th Edition):

Laber, Joshua Ryan. “The effects of protein-protein interactions on in vitro and in vivo behavior of protein solutions.” 2017. Web. 17 Jan 2021.

Vancouver:

Laber JR. The effects of protein-protein interactions on in vitro and in vivo behavior of protein solutions. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/2152/72727.

Council of Science Editors:

Laber JR. The effects of protein-protein interactions on in vitro and in vivo behavior of protein solutions. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/72727


Cornell University

7. Anderson, Valerie. Alpha-Synuclein And Enhanced Green Fluorescent Protein In Trifluoroethanol: Protective Factors Oppose Protein Aggregation.

Degree: PhD, Physics, 2011, Cornell University

Protein aggregation, leading to the formation of amyloid fibrils, is associated with many human diseases, including Parkinson's disease, Alzheimer's disease and type II diabetes. 2,2,2-trifluoroethanol… (more)

Subjects/Keywords: trifluoroethanol; amyloid; protein aggregation

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APA (6th Edition):

Anderson, V. (2011). Alpha-Synuclein And Enhanced Green Fluorescent Protein In Trifluoroethanol: Protective Factors Oppose Protein Aggregation. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/30736

Chicago Manual of Style (16th Edition):

Anderson, Valerie. “Alpha-Synuclein And Enhanced Green Fluorescent Protein In Trifluoroethanol: Protective Factors Oppose Protein Aggregation.” 2011. Doctoral Dissertation, Cornell University. Accessed January 17, 2021. http://hdl.handle.net/1813/30736.

MLA Handbook (7th Edition):

Anderson, Valerie. “Alpha-Synuclein And Enhanced Green Fluorescent Protein In Trifluoroethanol: Protective Factors Oppose Protein Aggregation.” 2011. Web. 17 Jan 2021.

Vancouver:

Anderson V. Alpha-Synuclein And Enhanced Green Fluorescent Protein In Trifluoroethanol: Protective Factors Oppose Protein Aggregation. [Internet] [Doctoral dissertation]. Cornell University; 2011. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1813/30736.

Council of Science Editors:

Anderson V. Alpha-Synuclein And Enhanced Green Fluorescent Protein In Trifluoroethanol: Protective Factors Oppose Protein Aggregation. [Doctoral Dissertation]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/30736


University of Colorado

8. Cordes, Amanda. Complex Stability Behavior in Novel Protein Constructs: Aggregation of Fc- and HSA- Based Fusion Proteins.

Degree: PhD, Chemical & Biochemical Engineering, 2011, University of Colorado

  The development of protein based biopharmaceuticals has resulted in the ability to treat many serious conditions, including endogenous protein deficiencies, cancer and autoimmune disorders.… (more)

Subjects/Keywords: Aggregation; Formulation; Protein; Chemical Engineering

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APA (6th Edition):

Cordes, A. (2011). Complex Stability Behavior in Novel Protein Constructs: Aggregation of Fc- and HSA- Based Fusion Proteins. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/20

Chicago Manual of Style (16th Edition):

Cordes, Amanda. “Complex Stability Behavior in Novel Protein Constructs: Aggregation of Fc- and HSA- Based Fusion Proteins.” 2011. Doctoral Dissertation, University of Colorado. Accessed January 17, 2021. https://scholar.colorado.edu/chbe_gradetds/20.

MLA Handbook (7th Edition):

Cordes, Amanda. “Complex Stability Behavior in Novel Protein Constructs: Aggregation of Fc- and HSA- Based Fusion Proteins.” 2011. Web. 17 Jan 2021.

Vancouver:

Cordes A. Complex Stability Behavior in Novel Protein Constructs: Aggregation of Fc- and HSA- Based Fusion Proteins. [Internet] [Doctoral dissertation]. University of Colorado; 2011. [cited 2021 Jan 17]. Available from: https://scholar.colorado.edu/chbe_gradetds/20.

Council of Science Editors:

Cordes A. Complex Stability Behavior in Novel Protein Constructs: Aggregation of Fc- and HSA- Based Fusion Proteins. [Doctoral Dissertation]. University of Colorado; 2011. Available from: https://scholar.colorado.edu/chbe_gradetds/20


University of Waterloo

9. Trainor, Kyle. Adnectin Solubility and Dynamics.

Degree: 2019, University of Waterloo

 Rapid growth of the global market for monoclonal antibodies (mAbs) has generated considerable interest in the development of alternative molecules that facilitate rapid discovery and… (more)

Subjects/Keywords: protein; aggregation; solubility; dynamics; Adnectin

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APA (6th Edition):

Trainor, K. (2019). Adnectin Solubility and Dynamics. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/15234

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):

Trainor, Kyle. “Adnectin Solubility and Dynamics.” 2019. Thesis, University of Waterloo. Accessed January 17, 2021. http://hdl.handle.net/10012/15234.

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

MLA Handbook (7th Edition):

Trainor, Kyle. “Adnectin Solubility and Dynamics.” 2019. Web. 17 Jan 2021.

Vancouver:

Trainor K. Adnectin Solubility and Dynamics. [Internet] [Thesis]. University of Waterloo; 2019. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/10012/15234.

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

Council of Science Editors:

Trainor K. Adnectin Solubility and Dynamics. [Thesis]. University of Waterloo; 2019. Available from: http://hdl.handle.net/10012/15234

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


University of Missouri – Columbia

10. Morales Quiñones, Mariana. A unique way to form a vesicle: aminopeptidase 1 aggregation and its binding to receptor ATG19 for recruitment of autophagic proteins to form a vesicle in the cytoplasm-to-vacuole-targeting pathway in yeast.

Degree: 2011, University of Missouri – Columbia

 Misfolded protein aggregation causes disease and aging; autophagy counteracts this by eliminating damaged components, enabling cells to survive starvation. The Cytoplasm-to-vacuole-targeting (Cvt) pathway in yeast… (more)

Subjects/Keywords: aminopeptidase; autophagy; propeptide; protein aggregation

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APA (6th Edition):

Morales Quiñones, M. (2011). A unique way to form a vesicle: aminopeptidase 1 aggregation and its binding to receptor ATG19 for recruitment of autophagic proteins to form a vesicle in the cytoplasm-to-vacuole-targeting pathway in yeast. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/14442

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):

Morales Quiñones, Mariana. “A unique way to form a vesicle: aminopeptidase 1 aggregation and its binding to receptor ATG19 for recruitment of autophagic proteins to form a vesicle in the cytoplasm-to-vacuole-targeting pathway in yeast.” 2011. Thesis, University of Missouri – Columbia. Accessed January 17, 2021. http://hdl.handle.net/10355/14442.

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

MLA Handbook (7th Edition):

Morales Quiñones, Mariana. “A unique way to form a vesicle: aminopeptidase 1 aggregation and its binding to receptor ATG19 for recruitment of autophagic proteins to form a vesicle in the cytoplasm-to-vacuole-targeting pathway in yeast.” 2011. Web. 17 Jan 2021.

Vancouver:

Morales Quiñones M. A unique way to form a vesicle: aminopeptidase 1 aggregation and its binding to receptor ATG19 for recruitment of autophagic proteins to form a vesicle in the cytoplasm-to-vacuole-targeting pathway in yeast. [Internet] [Thesis]. University of Missouri – Columbia; 2011. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/10355/14442.

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

Council of Science Editors:

Morales Quiñones M. A unique way to form a vesicle: aminopeptidase 1 aggregation and its binding to receptor ATG19 for recruitment of autophagic proteins to form a vesicle in the cytoplasm-to-vacuole-targeting pathway in yeast. [Thesis]. University of Missouri – Columbia; 2011. Available from: http://hdl.handle.net/10355/14442

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


University of Southern California

11. Shah, Manali. Protein aggregation: current scenario and recent developments.

Degree: MS, Pharmaceutical Sciences, 2012, University of Southern California

Aggregation of proteins is the major topic of discussion and debate in the biopharmaceutical industry. Various chemical and physical properties of proteins have been studied… (more)

Subjects/Keywords: protein; aggregation; degenerative diseases; protein aggregates; aggregation detection techniques; protein aggregation diseases; mechanisms of protein aggregation

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APA (6th Edition):

Shah, M. (2012). Protein aggregation: current scenario and recent developments. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/41391/rec/5300

Chicago Manual of Style (16th Edition):

Shah, Manali. “Protein aggregation: current scenario and recent developments.” 2012. Masters Thesis, University of Southern California. Accessed January 17, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/41391/rec/5300.

MLA Handbook (7th Edition):

Shah, Manali. “Protein aggregation: current scenario and recent developments.” 2012. Web. 17 Jan 2021.

Vancouver:

Shah M. Protein aggregation: current scenario and recent developments. [Internet] [Masters thesis]. University of Southern California; 2012. [cited 2021 Jan 17]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/41391/rec/5300.

Council of Science Editors:

Shah M. Protein aggregation: current scenario and recent developments. [Masters Thesis]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/41391/rec/5300


University of Manchester

12. Gilburt, James. A study of folded, denatured and aggregated states during the refolding of inclusion body proteins.

Degree: PhD, 2016, University of Manchester

 The need to high quality therapeutic proteins has grown significantly in the past 30 years. Recombinant proteins are often produced from vectors inserted into E.… (more)

Subjects/Keywords: 572; Protein refolding; Aggregation

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

APA (6th Edition):

Gilburt, J. (2016). A study of folded, denatured and aggregated states during the refolding of inclusion body proteins. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/a-study-of-folded-denatured-and-aggregated-states-during-the-refolding-of-inclusion-body-proteins(2985ec97-94e6-416d-bfd3-03e23306566f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680030

Chicago Manual of Style (16th Edition):

Gilburt, James. “A study of folded, denatured and aggregated states during the refolding of inclusion body proteins.” 2016. Doctoral Dissertation, University of Manchester. Accessed January 17, 2021. https://www.research.manchester.ac.uk/portal/en/theses/a-study-of-folded-denatured-and-aggregated-states-during-the-refolding-of-inclusion-body-proteins(2985ec97-94e6-416d-bfd3-03e23306566f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680030.

MLA Handbook (7th Edition):

Gilburt, James. “A study of folded, denatured and aggregated states during the refolding of inclusion body proteins.” 2016. Web. 17 Jan 2021.

Vancouver:

Gilburt J. A study of folded, denatured and aggregated states during the refolding of inclusion body proteins. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2021 Jan 17]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/a-study-of-folded-denatured-and-aggregated-states-during-the-refolding-of-inclusion-body-proteins(2985ec97-94e6-416d-bfd3-03e23306566f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680030.

Council of Science Editors:

Gilburt J. A study of folded, denatured and aggregated states during the refolding of inclusion body proteins. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/a-study-of-folded-denatured-and-aggregated-states-during-the-refolding-of-inclusion-body-proteins(2985ec97-94e6-416d-bfd3-03e23306566f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680030


University of Texas – Austin

13. O'Connell, Jeremy Daniel 1982-. Systemic protein aggregation in stress and aging restructures cytoplasmic architecture.

Degree: PhD, Biochemistry, 2012, University of Texas – Austin

 A common maxim of protein biochemistry states, “structure is function.” This is generally just as true for an individual polypeptide chains as for multi-protein complexes.… (more)

Subjects/Keywords: Stress; Aging; Protein aggregation; Yeast

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APA (6th Edition):

O'Connell, J. D. 1. (2012). Systemic protein aggregation in stress and aging restructures cytoplasmic architecture. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/23384

Chicago Manual of Style (16th Edition):

O'Connell, Jeremy Daniel 1982-. “Systemic protein aggregation in stress and aging restructures cytoplasmic architecture.” 2012. Doctoral Dissertation, University of Texas – Austin. Accessed January 17, 2021. http://hdl.handle.net/2152/23384.

MLA Handbook (7th Edition):

O'Connell, Jeremy Daniel 1982-. “Systemic protein aggregation in stress and aging restructures cytoplasmic architecture.” 2012. Web. 17 Jan 2021.

Vancouver:

O'Connell JD1. Systemic protein aggregation in stress and aging restructures cytoplasmic architecture. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2012. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/2152/23384.

Council of Science Editors:

O'Connell JD1. Systemic protein aggregation in stress and aging restructures cytoplasmic architecture. [Doctoral Dissertation]. University of Texas – Austin; 2012. Available from: http://hdl.handle.net/2152/23384


Texas A&M University

14. 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 17, 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. 17 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 17]. 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 Manchester

15. Nuhu, Mariam. Protein-protein interactions and aggregation in biotherapeutics.

Degree: PhD, 2015, University of Manchester

Protein aggregation is a frequently cited problem during the development of liquid protein formulations, which is especially problematic since each protein exhibits different aggregation behaviour.… (more)

Subjects/Keywords: 572; biotherapeutics; formulation; protein-protein interaction; protein aggregation; excipients

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

APA (6th Edition):

Nuhu, M. (2015). Protein-protein interactions and aggregation in biotherapeutics. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/proteinprotein-interactions-and-aggregation-in-biotherapeutics(1dba3d89-1474-486c-9eb9-6e21b4616dd9).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727829

Chicago Manual of Style (16th Edition):

Nuhu, Mariam. “Protein-protein interactions and aggregation in biotherapeutics.” 2015. Doctoral Dissertation, University of Manchester. Accessed January 17, 2021. https://www.research.manchester.ac.uk/portal/en/theses/proteinprotein-interactions-and-aggregation-in-biotherapeutics(1dba3d89-1474-486c-9eb9-6e21b4616dd9).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727829.

MLA Handbook (7th Edition):

Nuhu, Mariam. “Protein-protein interactions and aggregation in biotherapeutics.” 2015. Web. 17 Jan 2021.

Vancouver:

Nuhu M. Protein-protein interactions and aggregation in biotherapeutics. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2021 Jan 17]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/proteinprotein-interactions-and-aggregation-in-biotherapeutics(1dba3d89-1474-486c-9eb9-6e21b4616dd9).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727829.

Council of Science Editors:

Nuhu M. Protein-protein interactions and aggregation in biotherapeutics. [Doctoral Dissertation]. University of Manchester; 2015. Available from: https://www.research.manchester.ac.uk/portal/en/theses/proteinprotein-interactions-and-aggregation-in-biotherapeutics(1dba3d89-1474-486c-9eb9-6e21b4616dd9).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727829


University of Kansas

16. Telikepalli, Srivalli. Aggregation of IgG mAb Biotherapeutics: Sources, Methods of Characterization, and Biological Implications.

Degree: PhD, Pharmaceutical Chemistry, 2014, University of Kansas

 One of the predominant concerns with protein therapeutics is their tendency to aggregate at various stages of protein production, purification, filling, transportation, and administration. This… (more)

Subjects/Keywords: Pharmaceutical sciences; Monoclonal antibodies; Protein; Protein Aggregation; Protein Particles; Subvisible Particles

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

APA (6th Edition):

Telikepalli, S. (2014). Aggregation of IgG mAb Biotherapeutics: Sources, Methods of Characterization, and Biological Implications. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/21650

Chicago Manual of Style (16th Edition):

Telikepalli, Srivalli. “Aggregation of IgG mAb Biotherapeutics: Sources, Methods of Characterization, and Biological Implications.” 2014. Doctoral Dissertation, University of Kansas. Accessed January 17, 2021. http://hdl.handle.net/1808/21650.

MLA Handbook (7th Edition):

Telikepalli, Srivalli. “Aggregation of IgG mAb Biotherapeutics: Sources, Methods of Characterization, and Biological Implications.” 2014. Web. 17 Jan 2021.

Vancouver:

Telikepalli S. Aggregation of IgG mAb Biotherapeutics: Sources, Methods of Characterization, and Biological Implications. [Internet] [Doctoral dissertation]. University of Kansas; 2014. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1808/21650.

Council of Science Editors:

Telikepalli S. Aggregation of IgG mAb Biotherapeutics: Sources, Methods of Characterization, and Biological Implications. [Doctoral Dissertation]. University of Kansas; 2014. Available from: http://hdl.handle.net/1808/21650


University of Manchester

17. Nuhu, Mariam. Protein-protein interactions and aggregation in biotherapeutics.

Degree: 2015, University of Manchester

Protein aggregation is a frequently cited problem during the development of liquid protein formulations, which is especially problematic since each protein exhibits different aggregation behaviour.… (more)

Subjects/Keywords: protein aggregation; protein-protein interaction; excipients; formulation; biotherapeutics

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APA (6th Edition):

Nuhu, M. (2015). Protein-protein interactions and aggregation in biotherapeutics. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:277397

Chicago Manual of Style (16th Edition):

Nuhu, Mariam. “Protein-protein interactions and aggregation in biotherapeutics.” 2015. Doctoral Dissertation, University of Manchester. Accessed January 17, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:277397.

MLA Handbook (7th Edition):

Nuhu, Mariam. “Protein-protein interactions and aggregation in biotherapeutics.” 2015. Web. 17 Jan 2021.

Vancouver:

Nuhu M. Protein-protein interactions and aggregation in biotherapeutics. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2021 Jan 17]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:277397.

Council of Science Editors:

Nuhu M. Protein-protein interactions and aggregation in biotherapeutics. [Doctoral Dissertation]. University of Manchester; 2015. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:277397


University of Delaware

18. O'Brien, Christopher J. Colloidal protein-protein interactions as a design target for aggregation resistance.

Degree: PhD, University of Delaware, Department of Chemical and Biomolecular Engineering, 2018, University of Delaware

 Proteins therapeutics have emerged as an important class of biological macromolecules with the potential to improve survival rates and quality of life of patients suffering… (more)

Subjects/Keywords: Biological sciences; Applied sciences; Protein aggregation; Protein engineering; Protein stability; Protein-protein interactions

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APA (6th Edition):

O'Brien, C. J. (2018). Colloidal protein-protein interactions as a design target for aggregation resistance. (Doctoral Dissertation). University of Delaware. Retrieved from http://udspace.udel.edu/handle/19716/23763

Chicago Manual of Style (16th Edition):

O'Brien, Christopher J. “Colloidal protein-protein interactions as a design target for aggregation resistance.” 2018. Doctoral Dissertation, University of Delaware. Accessed January 17, 2021. http://udspace.udel.edu/handle/19716/23763.

MLA Handbook (7th Edition):

O'Brien, Christopher J. “Colloidal protein-protein interactions as a design target for aggregation resistance.” 2018. Web. 17 Jan 2021.

Vancouver:

O'Brien CJ. Colloidal protein-protein interactions as a design target for aggregation resistance. [Internet] [Doctoral dissertation]. University of Delaware; 2018. [cited 2021 Jan 17]. Available from: http://udspace.udel.edu/handle/19716/23763.

Council of Science Editors:

O'Brien CJ. Colloidal protein-protein interactions as a design target for aggregation resistance. [Doctoral Dissertation]. University of Delaware; 2018. Available from: http://udspace.udel.edu/handle/19716/23763


University of Georgia

19. Kazmierski, Michelle Nicole. Thermally induced aggregation of whey proteins : characterization of protein isolates and beta-lactoglobulin/ pectin interactions.

Degree: 2014, University of Georgia

 Despite its widespread utilization, information relating to the characterization of commercially available whey protein isolate (WPI) is limited. Further insight into its behavior in mixed… (more)

Subjects/Keywords: Whey protein isolate; Heat-induced aggregation

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APA (6th Edition):

Kazmierski, M. N. (2014). Thermally induced aggregation of whey proteins : characterization of protein isolates and beta-lactoglobulin/ pectin interactions. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/20598

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):

Kazmierski, Michelle Nicole. “Thermally induced aggregation of whey proteins : characterization of protein isolates and beta-lactoglobulin/ pectin interactions.” 2014. Thesis, University of Georgia. Accessed January 17, 2021. http://hdl.handle.net/10724/20598.

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

MLA Handbook (7th Edition):

Kazmierski, Michelle Nicole. “Thermally induced aggregation of whey proteins : characterization of protein isolates and beta-lactoglobulin/ pectin interactions.” 2014. Web. 17 Jan 2021.

Vancouver:

Kazmierski MN. Thermally induced aggregation of whey proteins : characterization of protein isolates and beta-lactoglobulin/ pectin interactions. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/10724/20598.

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

Council of Science Editors:

Kazmierski MN. Thermally induced aggregation of whey proteins : characterization of protein isolates and beta-lactoglobulin/ pectin interactions. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/20598

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


McMaster University

20. Hung, Claudia Lin-Kar. Analysis of Huntingtin Protein Aggregation Mechanisms and the Development of a Clinically-Derived Human Cell Model of Huntington's Disease.

Degree: PhD, 2018, McMaster University

Neurodegenerative diseases are characterized by selective neuronal vulnerability and subsequent degeneration in specific areas of the brain. Huntington’s Disease (HD) is inherited as an autosomal… (more)

Subjects/Keywords: Huntington's Disease; Neurodegeneration; Cell Biology; Protein Aggregation

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

APA (6th Edition):

Hung, C. L. (2018). Analysis of Huntingtin Protein Aggregation Mechanisms and the Development of a Clinically-Derived Human Cell Model of Huntington's Disease. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/23640

Chicago Manual of Style (16th Edition):

Hung, Claudia Lin-Kar. “Analysis of Huntingtin Protein Aggregation Mechanisms and the Development of a Clinically-Derived Human Cell Model of Huntington's Disease.” 2018. Doctoral Dissertation, McMaster University. Accessed January 17, 2021. http://hdl.handle.net/11375/23640.

MLA Handbook (7th Edition):

Hung, Claudia Lin-Kar. “Analysis of Huntingtin Protein Aggregation Mechanisms and the Development of a Clinically-Derived Human Cell Model of Huntington's Disease.” 2018. Web. 17 Jan 2021.

Vancouver:

Hung CL. Analysis of Huntingtin Protein Aggregation Mechanisms and the Development of a Clinically-Derived Human Cell Model of Huntington's Disease. [Internet] [Doctoral dissertation]. McMaster University; 2018. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/11375/23640.

Council of Science Editors:

Hung CL. Analysis of Huntingtin Protein Aggregation Mechanisms and the Development of a Clinically-Derived Human Cell Model of Huntington's Disease. [Doctoral Dissertation]. McMaster University; 2018. Available from: http://hdl.handle.net/11375/23640


University of Wollongong

21. Cox, Dezerae. The interaction of small heat shock molecular chaperone proteins with a-synuclein.

Degree: PhD, 2016, University of Wollongong

Protein homeostasis, or proteostasis, is the process of maintaining the conformational and functional integrity of the proteome. Proteostasis is preserved in the face of… (more)

Subjects/Keywords: protein aggregation; neurodegeneration; heat shock proteins

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APA (6th Edition):

Cox, D. (2016). The interaction of small heat shock molecular chaperone proteins with a-synuclein. (Doctoral Dissertation). University of Wollongong. Retrieved from 0601 BIOCHEMISTRY AND CELL BIOLOGY ; https://ro.uow.edu.au/theses/4823

Chicago Manual of Style (16th Edition):

Cox, Dezerae. “The interaction of small heat shock molecular chaperone proteins with a-synuclein.” 2016. Doctoral Dissertation, University of Wollongong. Accessed January 17, 2021. 0601 BIOCHEMISTRY AND CELL BIOLOGY ; https://ro.uow.edu.au/theses/4823.

MLA Handbook (7th Edition):

Cox, Dezerae. “The interaction of small heat shock molecular chaperone proteins with a-synuclein.” 2016. Web. 17 Jan 2021.

Vancouver:

Cox D. The interaction of small heat shock molecular chaperone proteins with a-synuclein. [Internet] [Doctoral dissertation]. University of Wollongong; 2016. [cited 2021 Jan 17]. Available from: 0601 BIOCHEMISTRY AND CELL BIOLOGY ; https://ro.uow.edu.au/theses/4823.

Council of Science Editors:

Cox D. The interaction of small heat shock molecular chaperone proteins with a-synuclein. [Doctoral Dissertation]. University of Wollongong; 2016. Available from: 0601 BIOCHEMISTRY AND CELL BIOLOGY ; https://ro.uow.edu.au/theses/4823

22. Morriss-Andrews, Herbert Alexander. Coarse-Grained Molecular Dynamics Simulations of Peptide Aggregation on Surfaces.

Degree: 2014, University of California – eScholarship, University of California

Protein aggregation involves self-assembly of normally soluble proteins or peptides into supramolecular structures. This process is particularly important due to its involvement in several amyloid… (more)

Subjects/Keywords: Biophysics; Aggregation; Membranes; Molecular Dynamics; Protein; Simulation

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APA (6th Edition):

Morriss-Andrews, H. A. (2014). Coarse-Grained Molecular Dynamics Simulations of Peptide Aggregation on Surfaces. (Thesis). University of California – eScholarship, University of California. Retrieved from http://www.escholarship.org/uc/item/2ms586vt

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):

Morriss-Andrews, Herbert Alexander. “Coarse-Grained Molecular Dynamics Simulations of Peptide Aggregation on Surfaces.” 2014. Thesis, University of California – eScholarship, University of California. Accessed January 17, 2021. http://www.escholarship.org/uc/item/2ms586vt.

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

MLA Handbook (7th Edition):

Morriss-Andrews, Herbert Alexander. “Coarse-Grained Molecular Dynamics Simulations of Peptide Aggregation on Surfaces.” 2014. Web. 17 Jan 2021.

Vancouver:

Morriss-Andrews HA. Coarse-Grained Molecular Dynamics Simulations of Peptide Aggregation on Surfaces. [Internet] [Thesis]. University of California – eScholarship, University of California; 2014. [cited 2021 Jan 17]. Available from: http://www.escholarship.org/uc/item/2ms586vt.

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

Council of Science Editors:

Morriss-Andrews HA. Coarse-Grained Molecular Dynamics Simulations of Peptide Aggregation on Surfaces. [Thesis]. University of California – eScholarship, University of California; 2014. Available from: http://www.escholarship.org/uc/item/2ms586vt

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


Virginia Tech

23. Ebanks, Keira C. Kinetics of Peptide Aggregation.

Degree: MS, Biological Systems Engineering, 2011, Virginia Tech

 The most thermodynamically stable biological structure is the cross-beta secondary structure of the "amyloid"or "prion". As a testament to its stability, the amyloid occurs naturally… (more)

Subjects/Keywords: protein aggregation; cross-beta; peptide; amyloids; kinetics

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APA (6th Edition):

Ebanks, K. C. (2011). Kinetics of Peptide Aggregation. (Masters Thesis). Virginia Tech. Retrieved from http://hdl.handle.net/10919/31830

Chicago Manual of Style (16th Edition):

Ebanks, Keira C. “Kinetics of Peptide Aggregation.” 2011. Masters Thesis, Virginia Tech. Accessed January 17, 2021. http://hdl.handle.net/10919/31830.

MLA Handbook (7th Edition):

Ebanks, Keira C. “Kinetics of Peptide Aggregation.” 2011. Web. 17 Jan 2021.

Vancouver:

Ebanks KC. Kinetics of Peptide Aggregation. [Internet] [Masters thesis]. Virginia Tech; 2011. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/10919/31830.

Council of Science Editors:

Ebanks KC. Kinetics of Peptide Aggregation. [Masters Thesis]. Virginia Tech; 2011. Available from: http://hdl.handle.net/10919/31830


University of Melbourne

24. WONG, YUAN QI. Defining the in vivo kinetics of mutant Huntingtin aggregation in a Drosophila model.

Degree: 2013, University of Melbourne

 Huntington’s Disease is caused by a polyQ expansion of ≥ 35Q in exon 1 of the IT15 gene which encodes the protein Huntingtin. Repeat length… (more)

Subjects/Keywords: Huntington's Disease; Dhunrosophila; protein aggregation; biochemistry

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APA (6th Edition):

WONG, Y. Q. (2013). Defining the in vivo kinetics of mutant Huntingtin aggregation in a Drosophila model. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/38434

Chicago Manual of Style (16th Edition):

WONG, YUAN QI. “Defining the in vivo kinetics of mutant Huntingtin aggregation in a Drosophila model.” 2013. Doctoral Dissertation, University of Melbourne. Accessed January 17, 2021. http://hdl.handle.net/11343/38434.

MLA Handbook (7th Edition):

WONG, YUAN QI. “Defining the in vivo kinetics of mutant Huntingtin aggregation in a Drosophila model.” 2013. Web. 17 Jan 2021.

Vancouver:

WONG YQ. Defining the in vivo kinetics of mutant Huntingtin aggregation in a Drosophila model. [Internet] [Doctoral dissertation]. University of Melbourne; 2013. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/11343/38434.

Council of Science Editors:

WONG YQ. Defining the in vivo kinetics of mutant Huntingtin aggregation in a Drosophila model. [Doctoral Dissertation]. University of Melbourne; 2013. Available from: http://hdl.handle.net/11343/38434


Clemson University

25. Wang, Bo. Understanding the Structure-Function Relationships of Dendrimers in Environmental and Biomedical Applications.

Degree: PhD, Physics and Astronomy, 2017, Clemson University

 We are living an era wherein nanoparticles (NPs) have been widely applied in our lives. Dendrimers are special polymeric NPs with unique physiochemical properties, which… (more)

Subjects/Keywords: biomedicine; biophysics; molecular simulation; nanoparticle; protein aggregation

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APA (6th Edition):

Wang, B. (2017). Understanding the Structure-Function Relationships of Dendrimers in Environmental and Biomedical Applications. (Doctoral Dissertation). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_dissertations/1967

Chicago Manual of Style (16th Edition):

Wang, Bo. “Understanding the Structure-Function Relationships of Dendrimers in Environmental and Biomedical Applications.” 2017. Doctoral Dissertation, Clemson University. Accessed January 17, 2021. https://tigerprints.clemson.edu/all_dissertations/1967.

MLA Handbook (7th Edition):

Wang, Bo. “Understanding the Structure-Function Relationships of Dendrimers in Environmental and Biomedical Applications.” 2017. Web. 17 Jan 2021.

Vancouver:

Wang B. Understanding the Structure-Function Relationships of Dendrimers in Environmental and Biomedical Applications. [Internet] [Doctoral dissertation]. Clemson University; 2017. [cited 2021 Jan 17]. Available from: https://tigerprints.clemson.edu/all_dissertations/1967.

Council of Science Editors:

Wang B. Understanding the Structure-Function Relationships of Dendrimers in Environmental and Biomedical Applications. [Doctoral Dissertation]. Clemson University; 2017. Available from: https://tigerprints.clemson.edu/all_dissertations/1967


University of Canterbury

26. Walker, Sophie Keziah. The aggregation of dihydrodipicolinate synthase.

Degree: PhD, 2008, University of Canterbury

 An increasing number of diseases are associated with protein misfolding, one type of which results in the formation of amyloid fibrils. This research has addressed… (more)

Subjects/Keywords: DHDPS; aggregation; protein

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APA (6th Edition):

Walker, S. K. (2008). The aggregation of dihydrodipicolinate synthase. (Doctoral Dissertation). University of Canterbury. Retrieved from http://dx.doi.org/10.26021/7667

Chicago Manual of Style (16th Edition):

Walker, Sophie Keziah. “The aggregation of dihydrodipicolinate synthase.” 2008. Doctoral Dissertation, University of Canterbury. Accessed January 17, 2021. http://dx.doi.org/10.26021/7667.

MLA Handbook (7th Edition):

Walker, Sophie Keziah. “The aggregation of dihydrodipicolinate synthase.” 2008. Web. 17 Jan 2021.

Vancouver:

Walker SK. The aggregation of dihydrodipicolinate synthase. [Internet] [Doctoral dissertation]. University of Canterbury; 2008. [cited 2021 Jan 17]. Available from: http://dx.doi.org/10.26021/7667.

Council of Science Editors:

Walker SK. The aggregation of dihydrodipicolinate synthase. [Doctoral Dissertation]. University of Canterbury; 2008. Available from: http://dx.doi.org/10.26021/7667


University of Sydney

27. Sifniotis, Vicki. Towards The Development of Biobetter Therapeutic Whole Antibodies .

Degree: 2019, University of Sydney

 The development of therapeutic antibodies has been revolutionary in the pharmaceutical industry due to the specificity of antibodies to a biological target and their ability… (more)

Subjects/Keywords: antibody; protein stability; formulation; aggregation; biopharmaceutic; affinity

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APA (6th Edition):

Sifniotis, V. (2019). Towards The Development of Biobetter Therapeutic Whole Antibodies . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/20829

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):

Sifniotis, Vicki. “Towards The Development of Biobetter Therapeutic Whole Antibodies .” 2019. Thesis, University of Sydney. Accessed January 17, 2021. http://hdl.handle.net/2123/20829.

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

MLA Handbook (7th Edition):

Sifniotis, Vicki. “Towards The Development of Biobetter Therapeutic Whole Antibodies .” 2019. Web. 17 Jan 2021.

Vancouver:

Sifniotis V. Towards The Development of Biobetter Therapeutic Whole Antibodies . [Internet] [Thesis]. University of Sydney; 2019. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/2123/20829.

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

Council of Science Editors:

Sifniotis V. Towards The Development of Biobetter Therapeutic Whole Antibodies . [Thesis]. University of Sydney; 2019. Available from: http://hdl.handle.net/2123/20829

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


Indian Institute of Science

28. Das, Anindita. Nanoparticle Mediated Suppression of Protein Aggregation.

Degree: PhD, Faculty of Science, 2018, Indian Institute of Science

 The increasing demands for biopharmaceuticals to treat different diseases have raised concerns about controlling the quality and efficacy of such pharmaceuticals. The design and formulation… (more)

Subjects/Keywords: Protein Aggregation; Biopharmaceuticals; Protein Aggregation Supression; Protein Adsorption; Protein Desorption; Silica Nanoparticle Synthetic Chaperones; Alcohol Dehydrogenase Thermal Aggregation; Insulin Chemical Aggregation; Nanoparticle Mediated Protein Aggregation Suppression; Gold Nanoparticle Synthetic Chaperones; Nanoparticle Protein Aggregation; Inorganic Chemistry

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APA (6th Edition):

Das, A. (2018). Nanoparticle Mediated Suppression of Protein Aggregation. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/3521

Chicago Manual of Style (16th Edition):

Das, Anindita. “Nanoparticle Mediated Suppression of Protein Aggregation.” 2018. Doctoral Dissertation, Indian Institute of Science. Accessed January 17, 2021. http://etd.iisc.ac.in/handle/2005/3521.

MLA Handbook (7th Edition):

Das, Anindita. “Nanoparticle Mediated Suppression of Protein Aggregation.” 2018. Web. 17 Jan 2021.

Vancouver:

Das A. Nanoparticle Mediated Suppression of Protein Aggregation. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2018. [cited 2021 Jan 17]. Available from: http://etd.iisc.ac.in/handle/2005/3521.

Council of Science Editors:

Das A. Nanoparticle Mediated Suppression of Protein Aggregation. [Doctoral Dissertation]. Indian Institute of Science; 2018. Available from: http://etd.iisc.ac.in/handle/2005/3521


University of Delaware

29. Barnett, Gregory V. Mechanistic insights into the role of protein interactions on the aggregation behavior of anti-streptavidin immunoglobulin gamma-1.

Degree: PhD, University of Delaware, Department of Chemical and Biomolecular Engineering, 2015, University of Delaware

 Monoclonal antibodies (mAbs) are one of the leading protein-based drug candidates in the biopharmaceutical industry. The formation of irreversible, non-native protein clusters (hereby called aggregates)… (more)

Subjects/Keywords: Protein-protein interactions.; Proteins.; Osmoregulation.; Water.; Aggregation (Chemistry); Streptavidin.; Immunoglobulins.

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APA (6th Edition):

Barnett, G. V. (2015). Mechanistic insights into the role of protein interactions on the aggregation behavior of anti-streptavidin immunoglobulin gamma-1. (Doctoral Dissertation). University of Delaware. Retrieved from http://udspace.udel.edu/handle/19716/17560

Chicago Manual of Style (16th Edition):

Barnett, Gregory V. “Mechanistic insights into the role of protein interactions on the aggregation behavior of anti-streptavidin immunoglobulin gamma-1.” 2015. Doctoral Dissertation, University of Delaware. Accessed January 17, 2021. http://udspace.udel.edu/handle/19716/17560.

MLA Handbook (7th Edition):

Barnett, Gregory V. “Mechanistic insights into the role of protein interactions on the aggregation behavior of anti-streptavidin immunoglobulin gamma-1.” 2015. Web. 17 Jan 2021.

Vancouver:

Barnett GV. Mechanistic insights into the role of protein interactions on the aggregation behavior of anti-streptavidin immunoglobulin gamma-1. [Internet] [Doctoral dissertation]. University of Delaware; 2015. [cited 2021 Jan 17]. Available from: http://udspace.udel.edu/handle/19716/17560.

Council of Science Editors:

Barnett GV. Mechanistic insights into the role of protein interactions on the aggregation behavior of anti-streptavidin immunoglobulin gamma-1. [Doctoral Dissertation]. University of Delaware; 2015. Available from: http://udspace.udel.edu/handle/19716/17560


Vrije Universiteit Amsterdam

30. Dijk, E. van. The role of hydrophobicity in protein folding and aggregation .

Degree: 2017, Vrije Universiteit Amsterdam

Subjects/Keywords: Protein Folding; Hydrophobicity; Protein aggregation

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APA (6th Edition):

Dijk, E. v. (2017). The role of hydrophobicity in protein folding and aggregation . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/55383

Chicago Manual of Style (16th Edition):

Dijk, E van. “The role of hydrophobicity in protein folding and aggregation .” 2017. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed January 17, 2021. http://hdl.handle.net/1871/55383.

MLA Handbook (7th Edition):

Dijk, E van. “The role of hydrophobicity in protein folding and aggregation .” 2017. Web. 17 Jan 2021.

Vancouver:

Dijk Ev. The role of hydrophobicity in protein folding and aggregation . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2017. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1871/55383.

Council of Science Editors:

Dijk Ev. The role of hydrophobicity in protein folding and aggregation . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2017. Available from: http://hdl.handle.net/1871/55383

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