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You searched for subject:( amyloid). Showing records 1 – 30 of 1255 total matches.

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University of Southern California

1. Okada, Alan Kiyoshi. Enhancing and inhibiting diabetic amyloid misfolding.

Degree: PhD, Integrative Biology of Disease, 2016, University of Southern California

 The misfolding and aggregation of proteins is associated with some of the most devastating diseases of the modern era, including type 2 diabetes mellitus, Alzheimer… (more)

Subjects/Keywords: diabetes; amyloid; islet amyloid polypeptide

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APA (6th Edition):

Okada, A. K. (2016). Enhancing and inhibiting diabetic amyloid misfolding. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/639571/rec/2381

Chicago Manual of Style (16th Edition):

Okada, Alan Kiyoshi. “Enhancing and inhibiting diabetic amyloid misfolding.” 2016. Doctoral Dissertation, University of Southern California. Accessed April 10, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/639571/rec/2381.

MLA Handbook (7th Edition):

Okada, Alan Kiyoshi. “Enhancing and inhibiting diabetic amyloid misfolding.” 2016. Web. 10 Apr 2021.

Vancouver:

Okada AK. Enhancing and inhibiting diabetic amyloid misfolding. [Internet] [Doctoral dissertation]. University of Southern California; 2016. [cited 2021 Apr 10]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/639571/rec/2381.

Council of Science Editors:

Okada AK. Enhancing and inhibiting diabetic amyloid misfolding. [Doctoral Dissertation]. University of Southern California; 2016. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/639571/rec/2381


Florida Atlantic University

2. Lantz, Richard. HUMAN CALCITONIN: AN INVESTIGATION OF AMYLOID FORMATION AND INHIBITION.

Degree: 2020, Florida Atlantic University

Human calcitonin (hCT) is a peptide hormone that is produced by the thyroid gland where it regulates blood calcium and stimulates bone formation. However, increased… (more)

Subjects/Keywords: Calcitonin; Amyloid

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APA (6th Edition):

Lantz, R. (2020). HUMAN CALCITONIN: AN INVESTIGATION OF AMYLOID FORMATION AND INHIBITION. (Thesis). Florida Atlantic University. Retrieved from http://fau.digital.flvc.org/islandora/object/fau:44433

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):

Lantz, Richard. “HUMAN CALCITONIN: AN INVESTIGATION OF AMYLOID FORMATION AND INHIBITION.” 2020. Thesis, Florida Atlantic University. Accessed April 10, 2021. http://fau.digital.flvc.org/islandora/object/fau:44433.

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

MLA Handbook (7th Edition):

Lantz, Richard. “HUMAN CALCITONIN: AN INVESTIGATION OF AMYLOID FORMATION AND INHIBITION.” 2020. Web. 10 Apr 2021.

Vancouver:

Lantz R. HUMAN CALCITONIN: AN INVESTIGATION OF AMYLOID FORMATION AND INHIBITION. [Internet] [Thesis]. Florida Atlantic University; 2020. [cited 2021 Apr 10]. Available from: http://fau.digital.flvc.org/islandora/object/fau:44433.

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

Council of Science Editors:

Lantz R. HUMAN CALCITONIN: AN INVESTIGATION OF AMYLOID FORMATION AND INHIBITION. [Thesis]. Florida Atlantic University; 2020. Available from: http://fau.digital.flvc.org/islandora/object/fau:44433

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


University of Rochester

3. Easterhoff, David. Characterization of Amyloid Fibrils in Seminal Fluid and Their Interaction With Pathogens.

Degree: PhD, 2013, University of Rochester

 Several proteolytic cleavage products of prostatic acid phosphatase and semenogelin have been identified in seminal fluid that are cationic in nature and have amyloidogenic propensity.… (more)

Subjects/Keywords: Amyloid Fibril; Fluorogenic Amyloid Dyes; SEVI; Semen-Associated Amyloid Fibrils

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APA (6th Edition):

Easterhoff, D. (2013). Characterization of Amyloid Fibrils in Seminal Fluid and Their Interaction With Pathogens. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/27256

Chicago Manual of Style (16th Edition):

Easterhoff, David. “Characterization of Amyloid Fibrils in Seminal Fluid and Their Interaction With Pathogens.” 2013. Doctoral Dissertation, University of Rochester. Accessed April 10, 2021. http://hdl.handle.net/1802/27256.

MLA Handbook (7th Edition):

Easterhoff, David. “Characterization of Amyloid Fibrils in Seminal Fluid and Their Interaction With Pathogens.” 2013. Web. 10 Apr 2021.

Vancouver:

Easterhoff D. Characterization of Amyloid Fibrils in Seminal Fluid and Their Interaction With Pathogens. [Internet] [Doctoral dissertation]. University of Rochester; 2013. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/1802/27256.

Council of Science Editors:

Easterhoff D. Characterization of Amyloid Fibrils in Seminal Fluid and Their Interaction With Pathogens. [Doctoral Dissertation]. University of Rochester; 2013. Available from: http://hdl.handle.net/1802/27256


Texas State University – San Marcos

4. Campbell, James. Optimization of SDD-AGE as a Method to Study Amyloid Conversion of Human Recombinant Prion Protein.

Degree: MS, Biochemistry, 2014, Texas State University – San Marcos

 Many common diseases are caused by amyloid proteins. Amyloid structures are β sheet rich, protease resistant, and can form polydisperse insoluble fibers. Due to these… (more)

Subjects/Keywords: SDD-AGE, Prion, Amyloid; Prion; Amyloid; Amyloid beta-protein; Amyloidosis; Prions; Recombinant proteins

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APA (6th Edition):

Campbell, J. (2014). Optimization of SDD-AGE as a Method to Study Amyloid Conversion of Human Recombinant Prion Protein. (Masters Thesis). Texas State University – San Marcos. Retrieved from https://digital.library.txstate.edu/handle/10877/5272

Chicago Manual of Style (16th Edition):

Campbell, James. “Optimization of SDD-AGE as a Method to Study Amyloid Conversion of Human Recombinant Prion Protein.” 2014. Masters Thesis, Texas State University – San Marcos. Accessed April 10, 2021. https://digital.library.txstate.edu/handle/10877/5272.

MLA Handbook (7th Edition):

Campbell, James. “Optimization of SDD-AGE as a Method to Study Amyloid Conversion of Human Recombinant Prion Protein.” 2014. Web. 10 Apr 2021.

Vancouver:

Campbell J. Optimization of SDD-AGE as a Method to Study Amyloid Conversion of Human Recombinant Prion Protein. [Internet] [Masters thesis]. Texas State University – San Marcos; 2014. [cited 2021 Apr 10]. Available from: https://digital.library.txstate.edu/handle/10877/5272.

Council of Science Editors:

Campbell J. Optimization of SDD-AGE as a Method to Study Amyloid Conversion of Human Recombinant Prion Protein. [Masters Thesis]. Texas State University – San Marcos; 2014. Available from: https://digital.library.txstate.edu/handle/10877/5272


NSYSU

5. Huang, Huei-Jhen. Influence of chemical conditions on human insulin fibril structure.

Degree: Master, Chemistry, 2013, NSYSU

 Many proteins can misfold to form non-native structures and induce aggregation. Previous studies had found that more than 20 kinds of proteins may cause specific… (more)

Subjects/Keywords: alcohol; amyloid; pH; peptide; insulin

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APA (6th Edition):

Huang, H. (2013). Influence of chemical conditions on human insulin fibril structure. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0713113-113753

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):

Huang, Huei-Jhen. “Influence of chemical conditions on human insulin fibril structure.” 2013. Thesis, NSYSU. Accessed April 10, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0713113-113753.

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

MLA Handbook (7th Edition):

Huang, Huei-Jhen. “Influence of chemical conditions on human insulin fibril structure.” 2013. Web. 10 Apr 2021.

Vancouver:

Huang H. Influence of chemical conditions on human insulin fibril structure. [Internet] [Thesis]. NSYSU; 2013. [cited 2021 Apr 10]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0713113-113753.

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

Council of Science Editors:

Huang H. Influence of chemical conditions on human insulin fibril structure. [Thesis]. NSYSU; 2013. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0713113-113753

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


NSYSU

6. Yang, Shu-Wei. Various insulin fibril surface charge distribution studied by Electrostatic Force Microscopy.

Degree: Master, Chemistry, 2012, NSYSU

 In this report, electrostatic force microscopy (EFM), zeta-potential analyzer, circular dichroism Spectrophotometer and Fourier transform infrared spectroscopy are used to study the electrostatic property of… (more)

Subjects/Keywords: freezing; salt; EFM; amyloid; insulin

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APA (6th Edition):

Yang, S. (2012). Various insulin fibril surface charge distribution studied by Electrostatic Force Microscopy. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0803112-155349

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):

Yang, Shu-Wei. “Various insulin fibril surface charge distribution studied by Electrostatic Force Microscopy.” 2012. Thesis, NSYSU. Accessed April 10, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0803112-155349.

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

MLA Handbook (7th Edition):

Yang, Shu-Wei. “Various insulin fibril surface charge distribution studied by Electrostatic Force Microscopy.” 2012. Web. 10 Apr 2021.

Vancouver:

Yang S. Various insulin fibril surface charge distribution studied by Electrostatic Force Microscopy. [Internet] [Thesis]. NSYSU; 2012. [cited 2021 Apr 10]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0803112-155349.

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

Council of Science Editors:

Yang S. Various insulin fibril surface charge distribution studied by Electrostatic Force Microscopy. [Thesis]. NSYSU; 2012. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0803112-155349

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


NSYSU

7. Chang, Chiung-Wen. Investigation of the Insulin Amyloid Fibrils Structural Information by Atomic Force Microscope.

Degree: Master, Chemistry, 2011, NSYSU

 We study the conformational change of insulin fibril growth from three aspects: the impact of (i) incubation time; (ⅱ) nano-particles; (iii) and ion added. We… (more)

Subjects/Keywords: salt; nanoparticle; AFM; amyloid; Insulin

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APA (6th Edition):

Chang, C. (2011). Investigation of the Insulin Amyloid Fibrils Structural Information by Atomic Force Microscope. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0802111-124018

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):

Chang, Chiung-Wen. “Investigation of the Insulin Amyloid Fibrils Structural Information by Atomic Force Microscope.” 2011. Thesis, NSYSU. Accessed April 10, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0802111-124018.

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

MLA Handbook (7th Edition):

Chang, Chiung-Wen. “Investigation of the Insulin Amyloid Fibrils Structural Information by Atomic Force Microscope.” 2011. Web. 10 Apr 2021.

Vancouver:

Chang C. Investigation of the Insulin Amyloid Fibrils Structural Information by Atomic Force Microscope. [Internet] [Thesis]. NSYSU; 2011. [cited 2021 Apr 10]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0802111-124018.

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

Council of Science Editors:

Chang C. Investigation of the Insulin Amyloid Fibrils Structural Information by Atomic Force Microscope. [Thesis]. NSYSU; 2011. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0802111-124018

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


University of Tasmania

8. Hu, Y. Role of amyloid precursor protein in neural stem/progenitor cell proliferation and differentiation.

Degree: 2016, University of Tasmania

 Alzheimer’s disease (AD) is a progressive neurodegenerative condition that commonly affects people over the age of 65. There are currently no effective treatments which prevent… (more)

Subjects/Keywords: Amyloid; stem; proliferation; differentiation

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APA (6th Edition):

Hu, Y. (2016). Role of amyloid precursor protein in neural stem/progenitor cell proliferation and differentiation. (Thesis). University of Tasmania. Retrieved from https://eprints.utas.edu.au/23030/1/Hu_whole_thesis.pdf

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

Chicago Manual of Style (16th Edition):

Hu, Y. “Role of amyloid precursor protein in neural stem/progenitor cell proliferation and differentiation.” 2016. Thesis, University of Tasmania. Accessed April 10, 2021. https://eprints.utas.edu.au/23030/1/Hu_whole_thesis.pdf.

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

MLA Handbook (7th Edition):

Hu, Y. “Role of amyloid precursor protein in neural stem/progenitor cell proliferation and differentiation.” 2016. Web. 10 Apr 2021.

Vancouver:

Hu Y. Role of amyloid precursor protein in neural stem/progenitor cell proliferation and differentiation. [Internet] [Thesis]. University of Tasmania; 2016. [cited 2021 Apr 10]. Available from: https://eprints.utas.edu.au/23030/1/Hu_whole_thesis.pdf.

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

Council of Science Editors:

Hu Y. Role of amyloid precursor protein in neural stem/progenitor cell proliferation and differentiation. [Thesis]. University of Tasmania; 2016. Available from: https://eprints.utas.edu.au/23030/1/Hu_whole_thesis.pdf

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

9. Pithadia, Amit S. Using Small Molecules and Peptides as Chemical Tools to Study Metal-Amyloid, Membrane-Amyloid, and Peptide-Amyloid Interactions.

Degree: PhD, Chemistry, 2016, University of Michigan

Amyloid proteins are a family a proteins that are characterized by the misfolding an intrinsically disordered monomer subunit into an ordered beta-sheet fibril. Recent evidence… (more)

Subjects/Keywords: Amyloid; small molecule; Chemistry; Science

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APA (6th Edition):

Pithadia, A. S. (2016). Using Small Molecules and Peptides as Chemical Tools to Study Metal-Amyloid, Membrane-Amyloid, and Peptide-Amyloid Interactions. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/120866

Chicago Manual of Style (16th Edition):

Pithadia, Amit S. “Using Small Molecules and Peptides as Chemical Tools to Study Metal-Amyloid, Membrane-Amyloid, and Peptide-Amyloid Interactions.” 2016. Doctoral Dissertation, University of Michigan. Accessed April 10, 2021. http://hdl.handle.net/2027.42/120866.

MLA Handbook (7th Edition):

Pithadia, Amit S. “Using Small Molecules and Peptides as Chemical Tools to Study Metal-Amyloid, Membrane-Amyloid, and Peptide-Amyloid Interactions.” 2016. Web. 10 Apr 2021.

Vancouver:

Pithadia AS. Using Small Molecules and Peptides as Chemical Tools to Study Metal-Amyloid, Membrane-Amyloid, and Peptide-Amyloid Interactions. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/2027.42/120866.

Council of Science Editors:

Pithadia AS. Using Small Molecules and Peptides as Chemical Tools to Study Metal-Amyloid, Membrane-Amyloid, and Peptide-Amyloid Interactions. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/120866


University of Manchester

10. Howard, Daniel. The role of the cytoskeleton in Alzheimer’s disease: a Drosophila perspective.

Degree: 2016, University of Manchester

 Alzheimer’s disease (AD) pathogenesis is likely to be caused by dysfunction of two neuronal proteins, amyloid-beta (Aβ) and tau. Whilst excellent in vivo assays have… (more)

Subjects/Keywords: drosophila; neurodegeneration; amyloid; tau

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APA (6th Edition):

Howard, D. (2016). The role of the cytoskeleton in Alzheimer’s disease: a Drosophila perspective. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:300556

Chicago Manual of Style (16th Edition):

Howard, Daniel. “The role of the cytoskeleton in Alzheimer’s disease: a Drosophila perspective.” 2016. Doctoral Dissertation, University of Manchester. Accessed April 10, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:300556.

MLA Handbook (7th Edition):

Howard, Daniel. “The role of the cytoskeleton in Alzheimer’s disease: a Drosophila perspective.” 2016. Web. 10 Apr 2021.

Vancouver:

Howard D. The role of the cytoskeleton in Alzheimer’s disease: a Drosophila perspective. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2021 Apr 10]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:300556.

Council of Science Editors:

Howard D. The role of the cytoskeleton in Alzheimer’s disease: a Drosophila perspective. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:300556


University of Manchester

11. Noble, Elizabeth. The molecular mechanisms linking amyloid-beta, the prion protein and tau in Alzheimer's disease.

Degree: 2017, University of Manchester

 Several lines of evidence suggest that the expression of the cellular prion protein (PrPC) is altered with age and in sporadic Alzheimer’s disease, however, published… (more)

Subjects/Keywords: Alzheimers; Amyloid; Prion protein; Tau

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APA (6th Edition):

Noble, E. (2017). The molecular mechanisms linking amyloid-beta, the prion protein and tau in Alzheimer's disease. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:306712

Chicago Manual of Style (16th Edition):

Noble, Elizabeth. “The molecular mechanisms linking amyloid-beta, the prion protein and tau in Alzheimer's disease.” 2017. Doctoral Dissertation, University of Manchester. Accessed April 10, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:306712.

MLA Handbook (7th Edition):

Noble, Elizabeth. “The molecular mechanisms linking amyloid-beta, the prion protein and tau in Alzheimer's disease.” 2017. Web. 10 Apr 2021.

Vancouver:

Noble E. The molecular mechanisms linking amyloid-beta, the prion protein and tau in Alzheimer's disease. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2021 Apr 10]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:306712.

Council of Science Editors:

Noble E. The molecular mechanisms linking amyloid-beta, the prion protein and tau in Alzheimer's disease. [Doctoral Dissertation]. University of Manchester; 2017. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:306712


Cornell University

12. 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 April 10, 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. 10 Apr 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 Apr 10]. 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 Manchester

13. Moreth, Jens. Characterisation of different amyloid-ß aggregates in Alzheimer's Disease.

Degree: 2012, University of Manchester

 Alzheimer’s disease (AD) is the most common form of dementia, with more than 25 million people worldwide suffering this progressive intellectual failure. The disease was… (more)

Subjects/Keywords: Alzheimer's Disease; Amyloid beta

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APA (6th Edition):

Moreth, J. (2012). Characterisation of different amyloid-ß aggregates in Alzheimer's Disease. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:164717

Chicago Manual of Style (16th Edition):

Moreth, Jens. “Characterisation of different amyloid-ß aggregates in Alzheimer's Disease.” 2012. Doctoral Dissertation, University of Manchester. Accessed April 10, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:164717.

MLA Handbook (7th Edition):

Moreth, Jens. “Characterisation of different amyloid-ß aggregates in Alzheimer's Disease.” 2012. Web. 10 Apr 2021.

Vancouver:

Moreth J. Characterisation of different amyloid-ß aggregates in Alzheimer's Disease. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2021 Apr 10]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:164717.

Council of Science Editors:

Moreth J. Characterisation of different amyloid-ß aggregates in Alzheimer's Disease. [Doctoral Dissertation]. University of Manchester; 2012. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:164717


University of Toronto

14. Zukotynski, Katherine. Associations of Amyloid Deposition and FDG Uptake in Aging and Cognitively Impaired Elders With and Without Moderate to Severe Periventricular White Matter Hyperintensities Using Simple Machine Learning Techniques.

Degree: PhD, 2020, University of Toronto

 Abstract Background: Cerebral small vessel disease (SVD) often coexists with Alzheimer’s Disease (AD), but subjects with significant SVD were usually considered mixed disease and excluded… (more)

Subjects/Keywords: Amyloid; Dementia; PET; 0541

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APA (6th Edition):

Zukotynski, K. (2020). Associations of Amyloid Deposition and FDG Uptake in Aging and Cognitively Impaired Elders With and Without Moderate to Severe Periventricular White Matter Hyperintensities Using Simple Machine Learning Techniques. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/101041

Chicago Manual of Style (16th Edition):

Zukotynski, Katherine. “Associations of Amyloid Deposition and FDG Uptake in Aging and Cognitively Impaired Elders With and Without Moderate to Severe Periventricular White Matter Hyperintensities Using Simple Machine Learning Techniques.” 2020. Doctoral Dissertation, University of Toronto. Accessed April 10, 2021. http://hdl.handle.net/1807/101041.

MLA Handbook (7th Edition):

Zukotynski, Katherine. “Associations of Amyloid Deposition and FDG Uptake in Aging and Cognitively Impaired Elders With and Without Moderate to Severe Periventricular White Matter Hyperintensities Using Simple Machine Learning Techniques.” 2020. Web. 10 Apr 2021.

Vancouver:

Zukotynski K. Associations of Amyloid Deposition and FDG Uptake in Aging and Cognitively Impaired Elders With and Without Moderate to Severe Periventricular White Matter Hyperintensities Using Simple Machine Learning Techniques. [Internet] [Doctoral dissertation]. University of Toronto; 2020. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/1807/101041.

Council of Science Editors:

Zukotynski K. Associations of Amyloid Deposition and FDG Uptake in Aging and Cognitively Impaired Elders With and Without Moderate to Severe Periventricular White Matter Hyperintensities Using Simple Machine Learning Techniques. [Doctoral Dissertation]. University of Toronto; 2020. Available from: http://hdl.handle.net/1807/101041


University of Manchester

15. Moreth, Jens. Characterisation of different amyloid-ß aggregates in Alzheimer's disease.

Degree: PhD, 2012, University of Manchester

 Alzheimer’s disease (AD) is the most common form of dementia, with more than 25 million people worldwide suffering this progressive intellectual failure. The disease was… (more)

Subjects/Keywords: 616.8; Alzheimer's Disease; Amyloid beta

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APA (6th Edition):

Moreth, J. (2012). Characterisation of different amyloid-ß aggregates in Alzheimer's disease. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-different-amyloidss-aggregates-in-alzheimers-disease(88c7e7d8-dd08-4559-aa20-40f26950f0d5).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.632161

Chicago Manual of Style (16th Edition):

Moreth, Jens. “Characterisation of different amyloid-ß aggregates in Alzheimer's disease.” 2012. Doctoral Dissertation, University of Manchester. Accessed April 10, 2021. https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-different-amyloidss-aggregates-in-alzheimers-disease(88c7e7d8-dd08-4559-aa20-40f26950f0d5).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.632161.

MLA Handbook (7th Edition):

Moreth, Jens. “Characterisation of different amyloid-ß aggregates in Alzheimer's disease.” 2012. Web. 10 Apr 2021.

Vancouver:

Moreth J. Characterisation of different amyloid-ß aggregates in Alzheimer's disease. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2021 Apr 10]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-different-amyloidss-aggregates-in-alzheimers-disease(88c7e7d8-dd08-4559-aa20-40f26950f0d5).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.632161.

Council of Science Editors:

Moreth J. Characterisation of different amyloid-ß aggregates in Alzheimer's disease. [Doctoral Dissertation]. University of Manchester; 2012. Available from: https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-different-amyloidss-aggregates-in-alzheimers-disease(88c7e7d8-dd08-4559-aa20-40f26950f0d5).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.632161


University of Melbourne

16. SAHATHEVAN, RAMESH. Beta amyloid deposition in infarct and peri-infarct areas assessed using 11C Pittsburg Compound B and positron emission tomography.

Degree: 2012, University of Melbourne

 Introduction: Alzheimer’s disease (AD) and vascular cognitive impairment (VCI) are the most common forms of dementia. There is epidemiological evidence that vascular risk factors are… (more)

Subjects/Keywords: stroke; amyloid; 11C-PiB-PET

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APA (6th Edition):

SAHATHEVAN, R. (2012). Beta amyloid deposition in infarct and peri-infarct areas assessed using 11C Pittsburg Compound B and positron emission tomography. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/37807

Chicago Manual of Style (16th Edition):

SAHATHEVAN, RAMESH. “Beta amyloid deposition in infarct and peri-infarct areas assessed using 11C Pittsburg Compound B and positron emission tomography.” 2012. Doctoral Dissertation, University of Melbourne. Accessed April 10, 2021. http://hdl.handle.net/11343/37807.

MLA Handbook (7th Edition):

SAHATHEVAN, RAMESH. “Beta amyloid deposition in infarct and peri-infarct areas assessed using 11C Pittsburg Compound B and positron emission tomography.” 2012. Web. 10 Apr 2021.

Vancouver:

SAHATHEVAN R. Beta amyloid deposition in infarct and peri-infarct areas assessed using 11C Pittsburg Compound B and positron emission tomography. [Internet] [Doctoral dissertation]. University of Melbourne; 2012. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/11343/37807.

Council of Science Editors:

SAHATHEVAN R. Beta amyloid deposition in infarct and peri-infarct areas assessed using 11C Pittsburg Compound B and positron emission tomography. [Doctoral Dissertation]. University of Melbourne; 2012. Available from: http://hdl.handle.net/11343/37807


University of Melbourne

17. JOHANSSEN, TIMOTHY. The Role of metals and Aβ in excitotoxicity and Alzheimer’s disease.

Degree: 2015, University of Melbourne

 Background: N-methyl-d-aspartate receptors (NMDARs) are ionotropic channels gated by the excitatory amino acid, glutamate. They play an essential role in synaptic plasticity, enhancing synaptic signal… (more)

Subjects/Keywords: Alzheimer's disease; beta amyloid; excitotoxicity

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APA (6th Edition):

JOHANSSEN, T. (2015). The Role of metals and Aβ in excitotoxicity and Alzheimer’s disease. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/55550

Chicago Manual of Style (16th Edition):

JOHANSSEN, TIMOTHY. “The Role of metals and Aβ in excitotoxicity and Alzheimer’s disease.” 2015. Doctoral Dissertation, University of Melbourne. Accessed April 10, 2021. http://hdl.handle.net/11343/55550.

MLA Handbook (7th Edition):

JOHANSSEN, TIMOTHY. “The Role of metals and Aβ in excitotoxicity and Alzheimer’s disease.” 2015. Web. 10 Apr 2021.

Vancouver:

JOHANSSEN T. The Role of metals and Aβ in excitotoxicity and Alzheimer’s disease. [Internet] [Doctoral dissertation]. University of Melbourne; 2015. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/11343/55550.

Council of Science Editors:

JOHANSSEN T. The Role of metals and Aβ in excitotoxicity and Alzheimer’s disease. [Doctoral Dissertation]. University of Melbourne; 2015. Available from: http://hdl.handle.net/11343/55550


University of Southern California

18. Cervantes Cortes, Silvia A. Structural characterization of the functional amyloid Orb2A using EPR spectroscopy.

Degree: MS, Biochemistry and Molecular Biology, 2015, University of Southern California

 Functional amyloids are responsible for a variety of physiological processes in a diverse range of organisms. In humans, Pmel17 is involved in the synthesis of… (more)

Subjects/Keywords: functional amyloid; Orb2A; EPR spectroscopy

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APA (6th Edition):

Cervantes Cortes, S. A. (2015). Structural characterization of the functional amyloid Orb2A using EPR spectroscopy. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/583308/rec/6120

Chicago Manual of Style (16th Edition):

Cervantes Cortes, Silvia A. “Structural characterization of the functional amyloid Orb2A using EPR spectroscopy.” 2015. Masters Thesis, University of Southern California. Accessed April 10, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/583308/rec/6120.

MLA Handbook (7th Edition):

Cervantes Cortes, Silvia A. “Structural characterization of the functional amyloid Orb2A using EPR spectroscopy.” 2015. Web. 10 Apr 2021.

Vancouver:

Cervantes Cortes SA. Structural characterization of the functional amyloid Orb2A using EPR spectroscopy. [Internet] [Masters thesis]. University of Southern California; 2015. [cited 2021 Apr 10]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/583308/rec/6120.

Council of Science Editors:

Cervantes Cortes SA. Structural characterization of the functional amyloid Orb2A using EPR spectroscopy. [Masters Thesis]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/583308/rec/6120


University of Hawaii – Manoa

19. Lawrence, James Le Marchant. N-terminal beta amyloid fragments regulate nicotinic acetylcholine receptors.

Degree: 2015, University of Hawaii – Manoa

Ph.D. University of Hawaii at Manoa 2014.

Soluble β-amyloid (Aβ) has been shown to regulate both presynaptic Ca2+ and synaptic plasticity. In particular picomolar concentrations… (more)

Subjects/Keywords: N-terminal beta amyloid fragments

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APA (6th Edition):

Lawrence, J. L. M. (2015). N-terminal beta amyloid fragments regulate nicotinic acetylcholine receptors. (Thesis). University of Hawaii – Manoa. Retrieved from http://hdl.handle.net/10125/101105

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):

Lawrence, James Le Marchant. “N-terminal beta amyloid fragments regulate nicotinic acetylcholine receptors.” 2015. Thesis, University of Hawaii – Manoa. Accessed April 10, 2021. http://hdl.handle.net/10125/101105.

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

MLA Handbook (7th Edition):

Lawrence, James Le Marchant. “N-terminal beta amyloid fragments regulate nicotinic acetylcholine receptors.” 2015. Web. 10 Apr 2021.

Vancouver:

Lawrence JLM. N-terminal beta amyloid fragments regulate nicotinic acetylcholine receptors. [Internet] [Thesis]. University of Hawaii – Manoa; 2015. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/10125/101105.

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

Council of Science Editors:

Lawrence JLM. N-terminal beta amyloid fragments regulate nicotinic acetylcholine receptors. [Thesis]. University of Hawaii – Manoa; 2015. Available from: http://hdl.handle.net/10125/101105

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


Louisiana State University

20. Bett, Cyrus Kipkurui. Amyloid Aggregation-Mitigating Peptides As Potential Alzheimer's Drugs.

Degree: PhD, Chemistry, 2009, Louisiana State University

 Neuronal cytotoxicity observed in Alzheimer¡¦s disease (AD) is linked to the aggregation of £]-amyloid peptide (A£]) into toxic forms. Increasing evidence points to oligomeric species… (more)

Subjects/Keywords: Amyloid aggregation

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APA (6th Edition):

Bett, C. K. (2009). Amyloid Aggregation-Mitigating Peptides As Potential Alzheimer's Drugs. (Doctoral Dissertation). Louisiana State University. Retrieved from etd-09012009-140708 ; https://digitalcommons.lsu.edu/gradschool_dissertations/1865

Chicago Manual of Style (16th Edition):

Bett, Cyrus Kipkurui. “Amyloid Aggregation-Mitigating Peptides As Potential Alzheimer's Drugs.” 2009. Doctoral Dissertation, Louisiana State University. Accessed April 10, 2021. etd-09012009-140708 ; https://digitalcommons.lsu.edu/gradschool_dissertations/1865.

MLA Handbook (7th Edition):

Bett, Cyrus Kipkurui. “Amyloid Aggregation-Mitigating Peptides As Potential Alzheimer's Drugs.” 2009. Web. 10 Apr 2021.

Vancouver:

Bett CK. Amyloid Aggregation-Mitigating Peptides As Potential Alzheimer's Drugs. [Internet] [Doctoral dissertation]. Louisiana State University; 2009. [cited 2021 Apr 10]. Available from: etd-09012009-140708 ; https://digitalcommons.lsu.edu/gradschool_dissertations/1865.

Council of Science Editors:

Bett CK. Amyloid Aggregation-Mitigating Peptides As Potential Alzheimer's Drugs. [Doctoral Dissertation]. Louisiana State University; 2009. Available from: etd-09012009-140708 ; https://digitalcommons.lsu.edu/gradschool_dissertations/1865


University of South Carolina

21. Wang, Yiying. Stilbenes: Therapeutic Interventions Targeting Amyloid β Protein Aggregation In Alzheimer’s Disease.

Degree: PhD, Chemical Engineering, 2017, University of South Carolina

  Alzheimer’s disease (AD) is the most common form of dementia and accounts for 60-80 % of all dementia cases. In the United States, AD… (more)

Subjects/Keywords: Chemical Engineering; Engineering; Alzheime; Amyloid

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

APA (6th Edition):

Wang, Y. (2017). Stilbenes: Therapeutic Interventions Targeting Amyloid β Protein Aggregation In Alzheimer’s Disease. (Doctoral Dissertation). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/4314

Chicago Manual of Style (16th Edition):

Wang, Yiying. “Stilbenes: Therapeutic Interventions Targeting Amyloid β Protein Aggregation In Alzheimer’s Disease.” 2017. Doctoral Dissertation, University of South Carolina. Accessed April 10, 2021. https://scholarcommons.sc.edu/etd/4314.

MLA Handbook (7th Edition):

Wang, Yiying. “Stilbenes: Therapeutic Interventions Targeting Amyloid β Protein Aggregation In Alzheimer’s Disease.” 2017. Web. 10 Apr 2021.

Vancouver:

Wang Y. Stilbenes: Therapeutic Interventions Targeting Amyloid β Protein Aggregation In Alzheimer’s Disease. [Internet] [Doctoral dissertation]. University of South Carolina; 2017. [cited 2021 Apr 10]. Available from: https://scholarcommons.sc.edu/etd/4314.

Council of Science Editors:

Wang Y. Stilbenes: Therapeutic Interventions Targeting Amyloid β Protein Aggregation In Alzheimer’s Disease. [Doctoral Dissertation]. University of South Carolina; 2017. Available from: https://scholarcommons.sc.edu/etd/4314


Georgia Tech

22. Chandramowlishwaran, Pavithra. Prion nucleation and propagation by mammalian amyloidogenic proteins in yeast.

Degree: PhD, Biology, 2018, Georgia Tech

 Cross-β fibrous protein polymers or “amyloids” are associated with a variety of human and animal diseases, including Alzheimer’s disease (AD), Parkinson’s disease (PD), and Huntington’s… (more)

Subjects/Keywords: Nucleation; Propagation; Amyloid; Yeast; Prion

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APA (6th Edition):

Chandramowlishwaran, P. (2018). Prion nucleation and propagation by mammalian amyloidogenic proteins in yeast. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/61159

Chicago Manual of Style (16th Edition):

Chandramowlishwaran, Pavithra. “Prion nucleation and propagation by mammalian amyloidogenic proteins in yeast.” 2018. Doctoral Dissertation, Georgia Tech. Accessed April 10, 2021. http://hdl.handle.net/1853/61159.

MLA Handbook (7th Edition):

Chandramowlishwaran, Pavithra. “Prion nucleation and propagation by mammalian amyloidogenic proteins in yeast.” 2018. Web. 10 Apr 2021.

Vancouver:

Chandramowlishwaran P. Prion nucleation and propagation by mammalian amyloidogenic proteins in yeast. [Internet] [Doctoral dissertation]. Georgia Tech; 2018. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/1853/61159.

Council of Science Editors:

Chandramowlishwaran P. Prion nucleation and propagation by mammalian amyloidogenic proteins in yeast. [Doctoral Dissertation]. Georgia Tech; 2018. Available from: http://hdl.handle.net/1853/61159


University of Manchester

23. Jackson, Joshua Daniel. Investigating Therapeutic Strategies in a Preclinical Model for Alzheimer’s Disease.

Degree: 2017, University of Manchester

 Alzheimer’s disease (AD) is a worldwide, incurable disease, and the most common form of dementia. Numbers of cases are rising, and since its discovery the… (more)

Subjects/Keywords: Alzheimer; Disease Model; Amyloid

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APA (6th Edition):

Jackson, J. D. (2017). Investigating Therapeutic Strategies in a Preclinical Model for Alzheimer’s Disease. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:310577

Chicago Manual of Style (16th Edition):

Jackson, Joshua Daniel. “Investigating Therapeutic Strategies in a Preclinical Model for Alzheimer’s Disease.” 2017. Doctoral Dissertation, University of Manchester. Accessed April 10, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:310577.

MLA Handbook (7th Edition):

Jackson, Joshua Daniel. “Investigating Therapeutic Strategies in a Preclinical Model for Alzheimer’s Disease.” 2017. Web. 10 Apr 2021.

Vancouver:

Jackson JD. Investigating Therapeutic Strategies in a Preclinical Model for Alzheimer’s Disease. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2021 Apr 10]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:310577.

Council of Science Editors:

Jackson JD. Investigating Therapeutic Strategies in a Preclinical Model for Alzheimer’s Disease. [Doctoral Dissertation]. University of Manchester; 2017. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:310577


Vanderbilt University

24. Barton, Shawn Michael. Innovations in Delivery of Theranostic Agents Across Biological Barriers for Applications in Alzheimer’s Disease.

Degree: PhD, Neuroscience, 2018, Vanderbilt University

 Alzheimer’s disease (AD) is a neurodegenerative disorder characterized by memory loss, language deficits, and executive dysfunction. Currently, there are no disease-modifying therapeutics available and major… (more)

Subjects/Keywords: Alzheimers; amyloid; retina; 5XFAD

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APA (6th Edition):

Barton, S. M. (2018). Innovations in Delivery of Theranostic Agents Across Biological Barriers for Applications in Alzheimer’s Disease. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/15303

Chicago Manual of Style (16th Edition):

Barton, Shawn Michael. “Innovations in Delivery of Theranostic Agents Across Biological Barriers for Applications in Alzheimer’s Disease.” 2018. Doctoral Dissertation, Vanderbilt University. Accessed April 10, 2021. http://hdl.handle.net/1803/15303.

MLA Handbook (7th Edition):

Barton, Shawn Michael. “Innovations in Delivery of Theranostic Agents Across Biological Barriers for Applications in Alzheimer’s Disease.” 2018. Web. 10 Apr 2021.

Vancouver:

Barton SM. Innovations in Delivery of Theranostic Agents Across Biological Barriers for Applications in Alzheimer’s Disease. [Internet] [Doctoral dissertation]. Vanderbilt University; 2018. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/1803/15303.

Council of Science Editors:

Barton SM. Innovations in Delivery of Theranostic Agents Across Biological Barriers for Applications in Alzheimer’s Disease. [Doctoral Dissertation]. Vanderbilt University; 2018. Available from: http://hdl.handle.net/1803/15303


University of Pennsylvania

25. Ferrie, John Joseph. Combining Computational And Experimental Approaches To Study Disordered And Aggregation Prone Proteins.

Degree: 2019, University of Pennsylvania

 Over the past two decades disordered proteins have become more widely recognized, challenging the canonical structure-function paradigm associated with proteins. These highly dynamic proteins have… (more)

Subjects/Keywords: amyloid; fluorescence; modeling; Chemistry

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APA (6th Edition):

Ferrie, J. J. (2019). Combining Computational And Experimental Approaches To Study Disordered And Aggregation Prone Proteins. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/3586

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):

Ferrie, John Joseph. “Combining Computational And Experimental Approaches To Study Disordered And Aggregation Prone Proteins.” 2019. Thesis, University of Pennsylvania. Accessed April 10, 2021. https://repository.upenn.edu/edissertations/3586.

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

MLA Handbook (7th Edition):

Ferrie, John Joseph. “Combining Computational And Experimental Approaches To Study Disordered And Aggregation Prone Proteins.” 2019. Web. 10 Apr 2021.

Vancouver:

Ferrie JJ. Combining Computational And Experimental Approaches To Study Disordered And Aggregation Prone Proteins. [Internet] [Thesis]. University of Pennsylvania; 2019. [cited 2021 Apr 10]. Available from: https://repository.upenn.edu/edissertations/3586.

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

Council of Science Editors:

Ferrie JJ. Combining Computational And Experimental Approaches To Study Disordered And Aggregation Prone Proteins. [Thesis]. University of Pennsylvania; 2019. Available from: https://repository.upenn.edu/edissertations/3586

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


University of Canterbury

26. Domigan, Laura Joy. New nanomaterials: amyloid fibrils from waste proteins.

Degree: Doctor of Philosopy, Biochemistry, 2012, University of Canterbury

 The current landscape of nanotechnology has focussed attention on materials that self-assemble. The search for such materials has unsurprisingly led to the biological world, where… (more)

Subjects/Keywords: Amyloid fibrils; crystallins; nanomaterial

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APA (6th Edition):

Domigan, L. J. (2012). New nanomaterials: amyloid fibrils from waste proteins. (Doctoral Dissertation). University of Canterbury. Retrieved from http://dx.doi.org/10.26021/6175

Chicago Manual of Style (16th Edition):

Domigan, Laura Joy. “New nanomaterials: amyloid fibrils from waste proteins.” 2012. Doctoral Dissertation, University of Canterbury. Accessed April 10, 2021. http://dx.doi.org/10.26021/6175.

MLA Handbook (7th Edition):

Domigan, Laura Joy. “New nanomaterials: amyloid fibrils from waste proteins.” 2012. Web. 10 Apr 2021.

Vancouver:

Domigan LJ. New nanomaterials: amyloid fibrils from waste proteins. [Internet] [Doctoral dissertation]. University of Canterbury; 2012. [cited 2021 Apr 10]. Available from: http://dx.doi.org/10.26021/6175.

Council of Science Editors:

Domigan LJ. New nanomaterials: amyloid fibrils from waste proteins. [Doctoral Dissertation]. University of Canterbury; 2012. Available from: http://dx.doi.org/10.26021/6175


University of Canterbury

27. Raynes, Jared Kenneth. Immobilising biomolecules on amyloid fibrils for biotechnology applications.

Degree: PhD, Biochemistry, 2012, University of Canterbury

Amyloid fibrils are an insoluble, highly ordered, fibrous protein structure, which have increasingly been recognised as having bionanotechnology applications. Their ability to selfassemble allows a… (more)

Subjects/Keywords: Amyloid; Immobilisation; Enzymes; Biotechnology; Nanotechnology

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APA (6th Edition):

Raynes, J. K. (2012). Immobilising biomolecules on amyloid fibrils for biotechnology applications. (Doctoral Dissertation). University of Canterbury. Retrieved from http://dx.doi.org/10.26021/9083

Chicago Manual of Style (16th Edition):

Raynes, Jared Kenneth. “Immobilising biomolecules on amyloid fibrils for biotechnology applications.” 2012. Doctoral Dissertation, University of Canterbury. Accessed April 10, 2021. http://dx.doi.org/10.26021/9083.

MLA Handbook (7th Edition):

Raynes, Jared Kenneth. “Immobilising biomolecules on amyloid fibrils for biotechnology applications.” 2012. Web. 10 Apr 2021.

Vancouver:

Raynes JK. Immobilising biomolecules on amyloid fibrils for biotechnology applications. [Internet] [Doctoral dissertation]. University of Canterbury; 2012. [cited 2021 Apr 10]. Available from: http://dx.doi.org/10.26021/9083.

Council of Science Editors:

Raynes JK. Immobilising biomolecules on amyloid fibrils for biotechnology applications. [Doctoral Dissertation]. University of Canterbury; 2012. Available from: http://dx.doi.org/10.26021/9083


NSYSU

28. Li, Yu-Ru. To Explore β-Amyloid Induced Oxidative DNA Damage and Repair in Rat Primary Cortical Neurons.

Degree: Master, Biological Sciences, 2016, NSYSU

 Alzheimer's disease (AD) is one of the common form of age-related neurodegenerative diseases and the leading cause of senile dementia. In the beta-amyloid (Aβ) cascade… (more)

Subjects/Keywords: β-amyloid; Amyloid precursor protein; Alzheimer's disease; DNA repair; Neurotoxicity

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APA (6th Edition):

Li, Y. (2016). To Explore β-Amyloid Induced Oxidative DNA Damage and Repair in Rat Primary Cortical Neurons. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1103115-165537

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):

Li, Yu-Ru. “To Explore β-Amyloid Induced Oxidative DNA Damage and Repair in Rat Primary Cortical Neurons.” 2016. Thesis, NSYSU. Accessed April 10, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1103115-165537.

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

MLA Handbook (7th Edition):

Li, Yu-Ru. “To Explore β-Amyloid Induced Oxidative DNA Damage and Repair in Rat Primary Cortical Neurons.” 2016. Web. 10 Apr 2021.

Vancouver:

Li Y. To Explore β-Amyloid Induced Oxidative DNA Damage and Repair in Rat Primary Cortical Neurons. [Internet] [Thesis]. NSYSU; 2016. [cited 2021 Apr 10]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1103115-165537.

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

Council of Science Editors:

Li Y. To Explore β-Amyloid Induced Oxidative DNA Damage and Repair in Rat Primary Cortical Neurons. [Thesis]. NSYSU; 2016. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1103115-165537

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


University of the Western Cape

29. Teponnou, Gerard A. Kenfack. Tacrine, trolox and tryptoline as lead compounds for the design and synthesis of multi-target drugs for Alzheimer's disease therapy .

Degree: 2016, University of the Western Cape

 The cascade of neurotoxic events involved in the pathogenesis of Alzheimer's disease may explain the inefficacy of currently available treatment based on acetylcholinesterase inhibitors (AChEI… (more)

Subjects/Keywords: Amyloid Beta; Cholinesterases; Alzheimer's disease; Multifunctional drugs; Amyloid beta-protein

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APA (6th Edition):

Teponnou, G. A. K. (2016). Tacrine, trolox and tryptoline as lead compounds for the design and synthesis of multi-target drugs for Alzheimer's disease therapy . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/5344

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):

Teponnou, Gerard A Kenfack. “Tacrine, trolox and tryptoline as lead compounds for the design and synthesis of multi-target drugs for Alzheimer's disease therapy .” 2016. Thesis, University of the Western Cape. Accessed April 10, 2021. http://hdl.handle.net/11394/5344.

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

MLA Handbook (7th Edition):

Teponnou, Gerard A Kenfack. “Tacrine, trolox and tryptoline as lead compounds for the design and synthesis of multi-target drugs for Alzheimer's disease therapy .” 2016. Web. 10 Apr 2021.

Vancouver:

Teponnou GAK. Tacrine, trolox and tryptoline as lead compounds for the design and synthesis of multi-target drugs for Alzheimer's disease therapy . [Internet] [Thesis]. University of the Western Cape; 2016. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/11394/5344.

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

Council of Science Editors:

Teponnou GAK. Tacrine, trolox and tryptoline as lead compounds for the design and synthesis of multi-target drugs for Alzheimer's disease therapy . [Thesis]. University of the Western Cape; 2016. Available from: http://hdl.handle.net/11394/5344

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


Université Montpellier II

30. Ahmed, Abdullah. Dévelopement d'une méthode bio-informatique pour la prédiction des régions amyloidogéniques dans les protéines. : Development of bioinformatics method for prediction of amyloidogenic regions in proteins.

Degree: Docteur es, Biologie Santé, 2013, Université Montpellier II

La formation d'agrégats protéiques insolubles et fibreux, appelés fibrilles amyloïdes, est impliquée dans une large variété de maladies humaines. Parmi elles, figurent entre autres, le… (more)

Subjects/Keywords: Bioinformatique; Amyloid; Maladie neurodégénérative; Bioinformatics; Amyloid; Neurodegenerative disease; Protein misfolding

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

APA (6th Edition):

Ahmed, A. (2013). Dévelopement d'une méthode bio-informatique pour la prédiction des régions amyloidogéniques dans les protéines. : Development of bioinformatics method for prediction of amyloidogenic regions in proteins. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2013MON20051

Chicago Manual of Style (16th Edition):

Ahmed, Abdullah. “Dévelopement d'une méthode bio-informatique pour la prédiction des régions amyloidogéniques dans les protéines. : Development of bioinformatics method for prediction of amyloidogenic regions in proteins.” 2013. Doctoral Dissertation, Université Montpellier II. Accessed April 10, 2021. http://www.theses.fr/2013MON20051.

MLA Handbook (7th Edition):

Ahmed, Abdullah. “Dévelopement d'une méthode bio-informatique pour la prédiction des régions amyloidogéniques dans les protéines. : Development of bioinformatics method for prediction of amyloidogenic regions in proteins.” 2013. Web. 10 Apr 2021.

Vancouver:

Ahmed A. Dévelopement d'une méthode bio-informatique pour la prédiction des régions amyloidogéniques dans les protéines. : Development of bioinformatics method for prediction of amyloidogenic regions in proteins. [Internet] [Doctoral dissertation]. Université Montpellier II; 2013. [cited 2021 Apr 10]. Available from: http://www.theses.fr/2013MON20051.

Council of Science Editors:

Ahmed A. Dévelopement d'une méthode bio-informatique pour la prédiction des régions amyloidogéniques dans les protéines. : Development of bioinformatics method for prediction of amyloidogenic regions in proteins. [Doctoral Dissertation]. Université Montpellier II; 2013. Available from: http://www.theses.fr/2013MON20051

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