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You searched for subject:(Peptide). Showing records 1 – 30 of 3239 total matches.

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University of Minnesota

1. Scott, Carolyn. Peptide-functionalized hydrogels for three-dimensional cell culture.

Degree: PhD, Biomedical Engineering, 2016, University of Minnesota

 Biomimetic scaffolds have played a major role in the advancements in tissue engineering. In addition to mimicking the stiffness, nanofibrous structure, and biochemistry of the… (more)

Subjects/Keywords: biomaterials; hydrogel; peptide; peptide-amphiphile

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APA (6th Edition):

Scott, C. (2016). Peptide-functionalized hydrogels for three-dimensional cell culture. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/185633

Chicago Manual of Style (16th Edition):

Scott, Carolyn. “Peptide-functionalized hydrogels for three-dimensional cell culture.” 2016. Doctoral Dissertation, University of Minnesota. Accessed November 26, 2020. http://hdl.handle.net/11299/185633.

MLA Handbook (7th Edition):

Scott, Carolyn. “Peptide-functionalized hydrogels for three-dimensional cell culture.” 2016. Web. 26 Nov 2020.

Vancouver:

Scott C. Peptide-functionalized hydrogels for three-dimensional cell culture. [Internet] [Doctoral dissertation]. University of Minnesota; 2016. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/11299/185633.

Council of Science Editors:

Scott C. Peptide-functionalized hydrogels for three-dimensional cell culture. [Doctoral Dissertation]. University of Minnesota; 2016. Available from: http://hdl.handle.net/11299/185633


Wake Forest University

2. Altamimi, Afnan M. TESTING THE EFFECT OF A NOVEL HYDROGEN SULFIDE RELEASING PEPTIDE ON INFECTED BURN WOUNDS.

Degree: 2019, Wake Forest University

 Burn wounds are a devastating form of injury that leads to substantial morbidity, mortality, and cost. One of the critical complications of burn wounds is… (more)

Subjects/Keywords: Antimicrobial Peptide

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APA (6th Edition):

Altamimi, A. M. (2019). TESTING THE EFFECT OF A NOVEL HYDROGEN SULFIDE RELEASING PEPTIDE ON INFECTED BURN WOUNDS. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/93900

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):

Altamimi, Afnan M. “TESTING THE EFFECT OF A NOVEL HYDROGEN SULFIDE RELEASING PEPTIDE ON INFECTED BURN WOUNDS.” 2019. Thesis, Wake Forest University. Accessed November 26, 2020. http://hdl.handle.net/10339/93900.

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

MLA Handbook (7th Edition):

Altamimi, Afnan M. “TESTING THE EFFECT OF A NOVEL HYDROGEN SULFIDE RELEASING PEPTIDE ON INFECTED BURN WOUNDS.” 2019. Web. 26 Nov 2020.

Vancouver:

Altamimi AM. TESTING THE EFFECT OF A NOVEL HYDROGEN SULFIDE RELEASING PEPTIDE ON INFECTED BURN WOUNDS. [Internet] [Thesis]. Wake Forest University; 2019. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/10339/93900.

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

Council of Science Editors:

Altamimi AM. TESTING THE EFFECT OF A NOVEL HYDROGEN SULFIDE RELEASING PEPTIDE ON INFECTED BURN WOUNDS. [Thesis]. Wake Forest University; 2019. Available from: http://hdl.handle.net/10339/93900

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


Université de Neuchâtel

3. Montandon, Cyrille. Identification and characterization of putative Toc159 interacting partners.

Degree: 2015, Université de Neuchâtel

 Le chloroplaste est l’organelle qui caractérise les plantes terrestres ainsi que les autres eucaryotes photosynthétiques. Il remplit diverses fonctions métaboliques, mais la photosynthèse est son… (more)

Subjects/Keywords: transit peptide

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APA (6th Edition):

Montandon, C. (2015). Identification and characterization of putative Toc159 interacting partners. (Thesis). Université de Neuchâtel. Retrieved from http://doc.rero.ch/record/257854

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):

Montandon, Cyrille. “Identification and characterization of putative Toc159 interacting partners.” 2015. Thesis, Université de Neuchâtel. Accessed November 26, 2020. http://doc.rero.ch/record/257854.

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

MLA Handbook (7th Edition):

Montandon, Cyrille. “Identification and characterization of putative Toc159 interacting partners.” 2015. Web. 26 Nov 2020.

Vancouver:

Montandon C. Identification and characterization of putative Toc159 interacting partners. [Internet] [Thesis]. Université de Neuchâtel; 2015. [cited 2020 Nov 26]. Available from: http://doc.rero.ch/record/257854.

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

Council of Science Editors:

Montandon C. Identification and characterization of putative Toc159 interacting partners. [Thesis]. Université de Neuchâtel; 2015. Available from: http://doc.rero.ch/record/257854

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

4. Cabalteja, Chino Cabasa. Bioengineering alpha conotoxin ViI : from disulfide bonds to native chemical ligation.

Degree: 2015, University of Hawaii – Manoa

M.S. University of Hawaii at Manoa 2014.

The paradigm of rational drug design has broadened its focus from classical small-molecule drugs and into larger biological… (more)

Subjects/Keywords: peptide isomers

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APA (6th Edition):

Cabalteja, C. C. (2015). Bioengineering alpha conotoxin ViI : from disulfide bonds to native chemical ligation. (Thesis). University of Hawaii – Manoa. Retrieved from http://hdl.handle.net/10125/100541

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):

Cabalteja, Chino Cabasa. “Bioengineering alpha conotoxin ViI : from disulfide bonds to native chemical ligation.” 2015. Thesis, University of Hawaii – Manoa. Accessed November 26, 2020. http://hdl.handle.net/10125/100541.

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

MLA Handbook (7th Edition):

Cabalteja, Chino Cabasa. “Bioengineering alpha conotoxin ViI : from disulfide bonds to native chemical ligation.” 2015. Web. 26 Nov 2020.

Vancouver:

Cabalteja CC. Bioengineering alpha conotoxin ViI : from disulfide bonds to native chemical ligation. [Internet] [Thesis]. University of Hawaii – Manoa; 2015. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/10125/100541.

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

Council of Science Editors:

Cabalteja CC. Bioengineering alpha conotoxin ViI : from disulfide bonds to native chemical ligation. [Thesis]. University of Hawaii – Manoa; 2015. Available from: http://hdl.handle.net/10125/100541

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


University of Sydney

5. Wang, Xiaoyi. Development and Application of Novel Methods for the Synthesis of Modified Proteins .

Degree: 2018, University of Sydney

 Proteins are essential biomolecules that mediate a range of biological processes in humans. Many proteins contain post-translational modifications (PTMs) that are often vital to their… (more)

Subjects/Keywords: peptide ligation

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APA (6th Edition):

Wang, X. (2018). Development and Application of Novel Methods for the Synthesis of Modified Proteins . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/19892

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):

Wang, Xiaoyi. “Development and Application of Novel Methods for the Synthesis of Modified Proteins .” 2018. Thesis, University of Sydney. Accessed November 26, 2020. http://hdl.handle.net/2123/19892.

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

MLA Handbook (7th Edition):

Wang, Xiaoyi. “Development and Application of Novel Methods for the Synthesis of Modified Proteins .” 2018. Web. 26 Nov 2020.

Vancouver:

Wang X. Development and Application of Novel Methods for the Synthesis of Modified Proteins . [Internet] [Thesis]. University of Sydney; 2018. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/2123/19892.

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

Council of Science Editors:

Wang X. Development and Application of Novel Methods for the Synthesis of Modified Proteins . [Thesis]. University of Sydney; 2018. Available from: http://hdl.handle.net/2123/19892

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


University of Manchester

6. Arthanari, Yamini. Study of cellular delivery of siRNA and shRNA targeting bcr-abl in chronic myeloid leukemia using Tat derived peptide.

Degree: 2011, University of Manchester

 Chronic Myeloid Leukemia is characterised by the formation of a fusion gene bcr-abl. The gene product BCR-ABL has deregulated tyrosine kinase activity that plays a… (more)

Subjects/Keywords: Cell penetrating peptide; Tat peptide; RNA interference

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APA (6th Edition):

Arthanari, Y. (2011). Study of cellular delivery of siRNA and shRNA targeting bcr-abl in chronic myeloid leukemia using Tat derived peptide. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:119786

Chicago Manual of Style (16th Edition):

Arthanari, Yamini. “Study of cellular delivery of siRNA and shRNA targeting bcr-abl in chronic myeloid leukemia using Tat derived peptide.” 2011. Doctoral Dissertation, University of Manchester. Accessed November 26, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:119786.

MLA Handbook (7th Edition):

Arthanari, Yamini. “Study of cellular delivery of siRNA and shRNA targeting bcr-abl in chronic myeloid leukemia using Tat derived peptide.” 2011. Web. 26 Nov 2020.

Vancouver:

Arthanari Y. Study of cellular delivery of siRNA and shRNA targeting bcr-abl in chronic myeloid leukemia using Tat derived peptide. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2020 Nov 26]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:119786.

Council of Science Editors:

Arthanari Y. Study of cellular delivery of siRNA and shRNA targeting bcr-abl in chronic myeloid leukemia using Tat derived peptide. [Doctoral Dissertation]. University of Manchester; 2011. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:119786


Georgia Tech

7. Sun, Yi. The PH dependent mechanisms of peptide bond cleavage.

Degree: MS, Chemical and Biomolecular Engineering, 2019, Georgia Tech

 The origin of life under prebiotic conditions has been an unsolved mystery for decades. Amino acids were available under prebiotic conditions, and different approaches of… (more)

Subjects/Keywords: Non-enzymatic peptide cleavage; Peptide degradation kinetics

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APA (6th Edition):

Sun, Y. (2019). The PH dependent mechanisms of peptide bond cleavage. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/62365

Chicago Manual of Style (16th Edition):

Sun, Yi. “The PH dependent mechanisms of peptide bond cleavage.” 2019. Masters Thesis, Georgia Tech. Accessed November 26, 2020. http://hdl.handle.net/1853/62365.

MLA Handbook (7th Edition):

Sun, Yi. “The PH dependent mechanisms of peptide bond cleavage.” 2019. Web. 26 Nov 2020.

Vancouver:

Sun Y. The PH dependent mechanisms of peptide bond cleavage. [Internet] [Masters thesis]. Georgia Tech; 2019. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1853/62365.

Council of Science Editors:

Sun Y. The PH dependent mechanisms of peptide bond cleavage. [Masters Thesis]. Georgia Tech; 2019. Available from: http://hdl.handle.net/1853/62365


Tulane University

8. Starr, Charles. Development of Novel Antimicrobial Peptides with Improved Hemocompatibility Through Combinatorial Library Screening and Rational Sequence Engineering.

Degree: 2017, Tulane University

Development of antimicrobial peptides (AMPs) as next generation clinical antibiotics has been a pursuit of the scientific community for several decades. AMPs are attractive drug… (more)

Subjects/Keywords: biochemistry; antimicrobial; peptide

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APA (6th Edition):

Starr, C. (2017). Development of Novel Antimicrobial Peptides with Improved Hemocompatibility Through Combinatorial Library Screening and Rational Sequence Engineering. (Thesis). Tulane University. Retrieved from https://digitallibrary.tulane.edu/islandora/object/tulane:77175

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):

Starr, Charles. “Development of Novel Antimicrobial Peptides with Improved Hemocompatibility Through Combinatorial Library Screening and Rational Sequence Engineering.” 2017. Thesis, Tulane University. Accessed November 26, 2020. https://digitallibrary.tulane.edu/islandora/object/tulane:77175.

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

MLA Handbook (7th Edition):

Starr, Charles. “Development of Novel Antimicrobial Peptides with Improved Hemocompatibility Through Combinatorial Library Screening and Rational Sequence Engineering.” 2017. Web. 26 Nov 2020.

Vancouver:

Starr C. Development of Novel Antimicrobial Peptides with Improved Hemocompatibility Through Combinatorial Library Screening and Rational Sequence Engineering. [Internet] [Thesis]. Tulane University; 2017. [cited 2020 Nov 26]. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:77175.

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

Council of Science Editors:

Starr C. Development of Novel Antimicrobial Peptides with Improved Hemocompatibility Through Combinatorial Library Screening and Rational Sequence Engineering. [Thesis]. Tulane University; 2017. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:77175

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


Tulane University

9. Guha, Shantanu. The Ebola virus delta-peptides are enterotoxic viroporins in vivo and potentially druggable targets.

Degree: 2020, Tulane University

[email protected]

During the 2013-2016 West African outbreak, severe gastrointestinal symptoms were common in Ebola patients and associated with poor outcome. The efficient spread of Ebola… (more)

Subjects/Keywords: ebola; peptide; antibody

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APA (6th Edition):

Guha, S. (2020). The Ebola virus delta-peptides are enterotoxic viroporins in vivo and potentially druggable targets. (Thesis). Tulane University. Retrieved from https://digitallibrary.tulane.edu/islandora/object/tulane:119728

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):

Guha, Shantanu. “The Ebola virus delta-peptides are enterotoxic viroporins in vivo and potentially druggable targets.” 2020. Thesis, Tulane University. Accessed November 26, 2020. https://digitallibrary.tulane.edu/islandora/object/tulane:119728.

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

MLA Handbook (7th Edition):

Guha, Shantanu. “The Ebola virus delta-peptides are enterotoxic viroporins in vivo and potentially druggable targets.” 2020. Web. 26 Nov 2020.

Vancouver:

Guha S. The Ebola virus delta-peptides are enterotoxic viroporins in vivo and potentially druggable targets. [Internet] [Thesis]. Tulane University; 2020. [cited 2020 Nov 26]. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:119728.

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

Council of Science Editors:

Guha S. The Ebola virus delta-peptides are enterotoxic viroporins in vivo and potentially druggable targets. [Thesis]. Tulane University; 2020. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:119728

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


University of Alberta

10. Lohans, Christopher T. Structural Characterization of Bacterial Antimicrobial Peptides.

Degree: PhD, Department of Chemistry, 2014, University of Alberta

 Paenibacillus polymyxa NRRL B-30509, Paenibacillus terrae NRRL B-30644 and P. polymyxa NRRL B-30507 were found to produce several bacteriocins and non-ribosomal peptides. All three strains… (more)

Subjects/Keywords: peptide; bacteriocin; antimicrobial

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APA (6th Edition):

Lohans, C. T. (2014). Structural Characterization of Bacterial Antimicrobial Peptides. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/8g84mn557

Chicago Manual of Style (16th Edition):

Lohans, Christopher T. “Structural Characterization of Bacterial Antimicrobial Peptides.” 2014. Doctoral Dissertation, University of Alberta. Accessed November 26, 2020. https://era.library.ualberta.ca/files/8g84mn557.

MLA Handbook (7th Edition):

Lohans, Christopher T. “Structural Characterization of Bacterial Antimicrobial Peptides.” 2014. Web. 26 Nov 2020.

Vancouver:

Lohans CT. Structural Characterization of Bacterial Antimicrobial Peptides. [Internet] [Doctoral dissertation]. University of Alberta; 2014. [cited 2020 Nov 26]. Available from: https://era.library.ualberta.ca/files/8g84mn557.

Council of Science Editors:

Lohans CT. Structural Characterization of Bacterial Antimicrobial Peptides. [Doctoral Dissertation]. University of Alberta; 2014. Available from: https://era.library.ualberta.ca/files/8g84mn557


University of Manchester

11. Wu, Ming-Cheng. Bio-engineering of Antibiotic Enduracidin Biosynthetic Pathways and PreQ1 Riboswitch.

Degree: 2011, University of Manchester

 Non-ribosomally synthesised natural products derived mainly from bacteria and fungi act as important therapeutic agents. Due to their complex structures it is difficult to chemically… (more)

Subjects/Keywords: non-ribosomal peptide

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APA (6th Edition):

Wu, M. (2011). Bio-engineering of Antibiotic Enduracidin Biosynthetic Pathways and PreQ1 Riboswitch. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:138266

Chicago Manual of Style (16th Edition):

Wu, Ming-Cheng. “Bio-engineering of Antibiotic Enduracidin Biosynthetic Pathways and PreQ1 Riboswitch.” 2011. Doctoral Dissertation, University of Manchester. Accessed November 26, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:138266.

MLA Handbook (7th Edition):

Wu, Ming-Cheng. “Bio-engineering of Antibiotic Enduracidin Biosynthetic Pathways and PreQ1 Riboswitch.” 2011. Web. 26 Nov 2020.

Vancouver:

Wu M. Bio-engineering of Antibiotic Enduracidin Biosynthetic Pathways and PreQ1 Riboswitch. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2020 Nov 26]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:138266.

Council of Science Editors:

Wu M. Bio-engineering of Antibiotic Enduracidin Biosynthetic Pathways and PreQ1 Riboswitch. [Doctoral Dissertation]. University of Manchester; 2011. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:138266


Mahatma Gandhi University

12. Sasikumar, P G. Solid phase peptide synthesis using glycerol based cross linked polymer supports.

Degree: 2010, Mahatma Gandhi University

 An important objective of the modem biochemical research is to understand the molecular basis of the numerous and intricate biological activities of peptides and proteins… (more)

Subjects/Keywords: Polimers; Peptide Synthesis

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APA (6th Edition):

Sasikumar, P. G. (2010). Solid phase peptide synthesis using glycerol based cross linked polymer supports. (Thesis). Mahatma Gandhi University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/302

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):

Sasikumar, P G. “Solid phase peptide synthesis using glycerol based cross linked polymer supports.” 2010. Thesis, Mahatma Gandhi University. Accessed November 26, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/302.

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

MLA Handbook (7th Edition):

Sasikumar, P G. “Solid phase peptide synthesis using glycerol based cross linked polymer supports.” 2010. Web. 26 Nov 2020.

Vancouver:

Sasikumar PG. Solid phase peptide synthesis using glycerol based cross linked polymer supports. [Internet] [Thesis]. Mahatma Gandhi University; 2010. [cited 2020 Nov 26]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/302.

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

Council of Science Editors:

Sasikumar PG. Solid phase peptide synthesis using glycerol based cross linked polymer supports. [Thesis]. Mahatma Gandhi University; 2010. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/302

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

13. Erhardt, Nola Marlene. The role of pituitary adenylate cyclase-activating polypeptide (PACAP) in cell cycle exit, differentiation and apoptosis during early chick brain development.

Degree: Department of Biology, 2017, University of Victoria

 Regulated survival, proliferation and differentiation of cells in the nervous system is crucial for development. Much of regulation is controlled by hormones. There is abundant… (more)

Subjects/Keywords: Peptide hormones; Hormones

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APA (6th Edition):

Erhardt, N. M. (2017). The role of pituitary adenylate cyclase-activating polypeptide (PACAP) in cell cycle exit, differentiation and apoptosis during early chick brain development. (Thesis). University of Victoria. Retrieved from http://hdl.handle.net/1828/7910

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):

Erhardt, Nola Marlene. “The role of pituitary adenylate cyclase-activating polypeptide (PACAP) in cell cycle exit, differentiation and apoptosis during early chick brain development.” 2017. Thesis, University of Victoria. Accessed November 26, 2020. http://hdl.handle.net/1828/7910.

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

MLA Handbook (7th Edition):

Erhardt, Nola Marlene. “The role of pituitary adenylate cyclase-activating polypeptide (PACAP) in cell cycle exit, differentiation and apoptosis during early chick brain development.” 2017. Web. 26 Nov 2020.

Vancouver:

Erhardt NM. The role of pituitary adenylate cyclase-activating polypeptide (PACAP) in cell cycle exit, differentiation and apoptosis during early chick brain development. [Internet] [Thesis]. University of Victoria; 2017. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1828/7910.

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

Council of Science Editors:

Erhardt NM. The role of pituitary adenylate cyclase-activating polypeptide (PACAP) in cell cycle exit, differentiation and apoptosis during early chick brain development. [Thesis]. University of Victoria; 2017. Available from: http://hdl.handle.net/1828/7910

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


University of Florida

14. Brice, David C. Innate Antiviral Defenses of Oral Epithelial Cells.

Degree: PhD, Medical Sciences - Immunology and Microbiology (IDP), 2018, University of Florida

 With many viruses spread via saliva, oral epithelial cells (OECs) act as one of the first barriers against infection of these pathogens. However, the defenses… (more)

Subjects/Keywords: immunity  – peptide  – virus

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APA (6th Edition):

Brice, D. C. (2018). Innate Antiviral Defenses of Oral Epithelial Cells. (Doctoral Dissertation). University of Florida. Retrieved from https://ufdc.ufl.edu/UFE0054013

Chicago Manual of Style (16th Edition):

Brice, David C. “Innate Antiviral Defenses of Oral Epithelial Cells.” 2018. Doctoral Dissertation, University of Florida. Accessed November 26, 2020. https://ufdc.ufl.edu/UFE0054013.

MLA Handbook (7th Edition):

Brice, David C. “Innate Antiviral Defenses of Oral Epithelial Cells.” 2018. Web. 26 Nov 2020.

Vancouver:

Brice DC. Innate Antiviral Defenses of Oral Epithelial Cells. [Internet] [Doctoral dissertation]. University of Florida; 2018. [cited 2020 Nov 26]. Available from: https://ufdc.ufl.edu/UFE0054013.

Council of Science Editors:

Brice DC. Innate Antiviral Defenses of Oral Epithelial Cells. [Doctoral Dissertation]. University of Florida; 2018. Available from: https://ufdc.ufl.edu/UFE0054013


University of Manchester

15. Szkolar, Laura. The Development of Functional Peptide Scaffolds for Cell Culture.

Degree: 2016, University of Manchester

 Peptides and peptide derivatives have shown great scope as biomaterials and for biomedicaltherapy application. It has been demonstrated that classes of these peptides can form… (more)

Subjects/Keywords: peptide; chondrocyte; hydrogel

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APA (6th Edition):

Szkolar, L. (2016). The Development of Functional Peptide Scaffolds for Cell Culture. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:298798

Chicago Manual of Style (16th Edition):

Szkolar, Laura. “The Development of Functional Peptide Scaffolds for Cell Culture.” 2016. Doctoral Dissertation, University of Manchester. Accessed November 26, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:298798.

MLA Handbook (7th Edition):

Szkolar, Laura. “The Development of Functional Peptide Scaffolds for Cell Culture.” 2016. Web. 26 Nov 2020.

Vancouver:

Szkolar L. The Development of Functional Peptide Scaffolds for Cell Culture. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2020 Nov 26]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:298798.

Council of Science Editors:

Szkolar L. The Development of Functional Peptide Scaffolds for Cell Culture. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:298798


University of New South Wales

16. Wang, Zhiyong. RGD peptide derivatives as tools for tumour imaging and therapy.

Degree: Chemical Sciences & Engineering, 2013, University of New South Wales

 The first project is a tumour imaging method based on iodinated micelle which can be applied as contrast agent for CT. the obtained micelle solution… (more)

Subjects/Keywords: Peptide; RGD; Fluorine

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APA (6th Edition):

Wang, Z. (2013). RGD peptide derivatives as tools for tumour imaging and therapy. (Masters Thesis). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/52850 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11523/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Wang, Zhiyong. “RGD peptide derivatives as tools for tumour imaging and therapy.” 2013. Masters Thesis, University of New South Wales. Accessed November 26, 2020. http://handle.unsw.edu.au/1959.4/52850 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11523/SOURCE01?view=true.

MLA Handbook (7th Edition):

Wang, Zhiyong. “RGD peptide derivatives as tools for tumour imaging and therapy.” 2013. Web. 26 Nov 2020.

Vancouver:

Wang Z. RGD peptide derivatives as tools for tumour imaging and therapy. [Internet] [Masters thesis]. University of New South Wales; 2013. [cited 2020 Nov 26]. Available from: http://handle.unsw.edu.au/1959.4/52850 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11523/SOURCE01?view=true.

Council of Science Editors:

Wang Z. RGD peptide derivatives as tools for tumour imaging and therapy. [Masters Thesis]. University of New South Wales; 2013. Available from: http://handle.unsw.edu.au/1959.4/52850 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11523/SOURCE01?view=true


University of Edinburgh

17. Svensen, Nina. Cellular analysis and PNA encoded libraries.

Degree: PhD, 2011, University of Edinburgh

 A peptide nucleic acid (PNA) encoded 1296 member peptide library was synthesised and incubated with a variety of cell types. Library members entering cells were… (more)

Subjects/Keywords: 572.8; peptide nucleic acid; peptide library; endocytic uptake mechanism; peptide-ligands

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APA (6th Edition):

Svensen, N. (2011). Cellular analysis and PNA encoded libraries. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/9605

Chicago Manual of Style (16th Edition):

Svensen, Nina. “Cellular analysis and PNA encoded libraries.” 2011. Doctoral Dissertation, University of Edinburgh. Accessed November 26, 2020. http://hdl.handle.net/1842/9605.

MLA Handbook (7th Edition):

Svensen, Nina. “Cellular analysis and PNA encoded libraries.” 2011. Web. 26 Nov 2020.

Vancouver:

Svensen N. Cellular analysis and PNA encoded libraries. [Internet] [Doctoral dissertation]. University of Edinburgh; 2011. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1842/9605.

Council of Science Editors:

Svensen N. Cellular analysis and PNA encoded libraries. [Doctoral Dissertation]. University of Edinburgh; 2011. Available from: http://hdl.handle.net/1842/9605


University of Cambridge

18. Brichtova, Eva. Studies on the physical stability of a C-terminally amidated variant of GLP-1.

Degree: MPhil, 2019, University of Cambridge

 The phenomenon of peptide and protein aggregation is of great biochemical importance. Not only is it a key feature of numerous neurodegenerative diseases such as… (more)

Subjects/Keywords: peptide aggregation; glucagon-like peptide 1; GLP-1; peptide therapeutics; peptide stability; off-pathway oligomers; peptide oligomers; amyloid fibrils; metastable oligomers; amyloid aggregates; peptide degradation; fibrillation; misfolding; diabetes

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APA (6th Edition):

Brichtova, E. (2019). Studies on the physical stability of a C-terminally amidated variant of GLP-1. (Masters Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/296886

Chicago Manual of Style (16th Edition):

Brichtova, Eva. “Studies on the physical stability of a C-terminally amidated variant of GLP-1.” 2019. Masters Thesis, University of Cambridge. Accessed November 26, 2020. https://www.repository.cam.ac.uk/handle/1810/296886.

MLA Handbook (7th Edition):

Brichtova, Eva. “Studies on the physical stability of a C-terminally amidated variant of GLP-1.” 2019. Web. 26 Nov 2020.

Vancouver:

Brichtova E. Studies on the physical stability of a C-terminally amidated variant of GLP-1. [Internet] [Masters thesis]. University of Cambridge; 2019. [cited 2020 Nov 26]. Available from: https://www.repository.cam.ac.uk/handle/1810/296886.

Council of Science Editors:

Brichtova E. Studies on the physical stability of a C-terminally amidated variant of GLP-1. [Masters Thesis]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/296886


University of Illinois – Chicago

19. Jaishankar, Dinesh. Engineering a Higher Efficacy Anti-Heparan Sulfate Peptide for an Entry-Based Antiviral Therapy.

Degree: 2017, University of Illinois – Chicago

 Primary and recurring herpes simplex virus-1 (HSV-1) infections can cause different pathologies in the eye and in severe cases it can result in permanent blindness.… (more)

Subjects/Keywords: peptide engineering; herpes simplex virus; contact lens; d-peptide; peptide therapeutics; cornea

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APA (6th Edition):

Jaishankar, D. (2017). Engineering a Higher Efficacy Anti-Heparan Sulfate Peptide for an Entry-Based Antiviral Therapy. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/22031

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):

Jaishankar, Dinesh. “Engineering a Higher Efficacy Anti-Heparan Sulfate Peptide for an Entry-Based Antiviral Therapy.” 2017. Thesis, University of Illinois – Chicago. Accessed November 26, 2020. http://hdl.handle.net/10027/22031.

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

MLA Handbook (7th Edition):

Jaishankar, Dinesh. “Engineering a Higher Efficacy Anti-Heparan Sulfate Peptide for an Entry-Based Antiviral Therapy.” 2017. Web. 26 Nov 2020.

Vancouver:

Jaishankar D. Engineering a Higher Efficacy Anti-Heparan Sulfate Peptide for an Entry-Based Antiviral Therapy. [Internet] [Thesis]. University of Illinois – Chicago; 2017. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/10027/22031.

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

Council of Science Editors:

Jaishankar D. Engineering a Higher Efficacy Anti-Heparan Sulfate Peptide for an Entry-Based Antiviral Therapy. [Thesis]. University of Illinois – Chicago; 2017. Available from: http://hdl.handle.net/10027/22031

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


NSYSU

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

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 November 26, 2020. 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. 26 Nov 2020.

Vancouver:

Huang H. Influence of chemical conditions on human insulin fibril structure. [Internet] [Thesis]. NSYSU; 2013. [cited 2020 Nov 26]. 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


Ruhr Universität Bochum

21. Penkova, Maya. Arginine and Tryptophan rich antimicrobial peptides (AMPs) : modifications, application and mode of action.

Degree: 2010, Ruhr Universität Bochum

 Da multiresistente Bakterienstämme ein häufiges Problem darstellen, besteht Bedarf an neuen Verbindungen, die keine Resistenzen hervorrufen. Eine solche Verbindungsklasse stellen die kationischen antimikrobiellen Peptide dar… (more)

Subjects/Keywords: Arginin; Tryptophan; Ferrocen; Peptide

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APA (6th Edition):

Penkova, M. (2010). Arginine and Tryptophan rich antimicrobial peptides (AMPs) : modifications, application and mode of action. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-30249

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):

Penkova, Maya. “Arginine and Tryptophan rich antimicrobial peptides (AMPs) : modifications, application and mode of action.” 2010. Thesis, Ruhr Universität Bochum. Accessed November 26, 2020. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-30249.

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

MLA Handbook (7th Edition):

Penkova, Maya. “Arginine and Tryptophan rich antimicrobial peptides (AMPs) : modifications, application and mode of action.” 2010. Web. 26 Nov 2020.

Vancouver:

Penkova M. Arginine and Tryptophan rich antimicrobial peptides (AMPs) : modifications, application and mode of action. [Internet] [Thesis]. Ruhr Universität Bochum; 2010. [cited 2020 Nov 26]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-30249.

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

Council of Science Editors:

Penkova M. Arginine and Tryptophan rich antimicrobial peptides (AMPs) : modifications, application and mode of action. [Thesis]. Ruhr Universität Bochum; 2010. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-30249

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


Ruhr Universität Bochum

22. Jaouhar, Mohamed. Expressionsanalyse antimikrobieller Peptide beim kutanen Lupus erythematodes.

Degree: 2013, Ruhr Universität Bochum

 In dieser Arbeit wurde die Expression sechs verschiedener antimikrobieller Peptide (hBD-1, -2, -3, RNase7, LL-37 und Psoriasin) bei drei Subtypen des kutanen Lupus erythematodes (CLE),… (more)

Subjects/Keywords: Genexpression; Immunsystem; Peptide; Hautkrankheit; Bindegewebskrankheit

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APA (6th Edition):

Jaouhar, M. (2013). Expressionsanalyse antimikrobieller Peptide beim kutanen Lupus erythematodes. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-39305

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):

Jaouhar, Mohamed. “Expressionsanalyse antimikrobieller Peptide beim kutanen Lupus erythematodes.” 2013. Thesis, Ruhr Universität Bochum. Accessed November 26, 2020. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-39305.

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

MLA Handbook (7th Edition):

Jaouhar, Mohamed. “Expressionsanalyse antimikrobieller Peptide beim kutanen Lupus erythematodes.” 2013. Web. 26 Nov 2020.

Vancouver:

Jaouhar M. Expressionsanalyse antimikrobieller Peptide beim kutanen Lupus erythematodes. [Internet] [Thesis]. Ruhr Universität Bochum; 2013. [cited 2020 Nov 26]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-39305.

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

Council of Science Editors:

Jaouhar M. Expressionsanalyse antimikrobieller Peptide beim kutanen Lupus erythematodes. [Thesis]. Ruhr Universität Bochum; 2013. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-39305

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


Oregon State University

23. Blanchard, David, L. (David Lee). Advanced studies on cyclic amino acids in neurological signaling and peptide antibiotics.

Degree: PhD, Pharmacy, 2009, Oregon State University

 L-pipecolic acid (L-PA) is the higher homolog of proline. It occurs naturally in many organisms, including primates, as an intermediate in lysine degradation. The pathway… (more)

Subjects/Keywords: enduracidin; Peptide antibiotics  – Development

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APA (6th Edition):

Blanchard, David, L. (. L. (2009). Advanced studies on cyclic amino acids in neurological signaling and peptide antibiotics. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/11418

Chicago Manual of Style (16th Edition):

Blanchard, David, L (David Lee). “Advanced studies on cyclic amino acids in neurological signaling and peptide antibiotics.” 2009. Doctoral Dissertation, Oregon State University. Accessed November 26, 2020. http://hdl.handle.net/1957/11418.

MLA Handbook (7th Edition):

Blanchard, David, L (David Lee). “Advanced studies on cyclic amino acids in neurological signaling and peptide antibiotics.” 2009. Web. 26 Nov 2020.

Vancouver:

Blanchard, David L(L. Advanced studies on cyclic amino acids in neurological signaling and peptide antibiotics. [Internet] [Doctoral dissertation]. Oregon State University; 2009. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1957/11418.

Council of Science Editors:

Blanchard, David L(L. Advanced studies on cyclic amino acids in neurological signaling and peptide antibiotics. [Doctoral Dissertation]. Oregon State University; 2009. Available from: http://hdl.handle.net/1957/11418


University of Alberta

24. Etayash, Hashem Ra. Engineering Surface-tethered Bacteriocins for Studying Peptide-bacteria Interactions.

Degree: MS, Faculty of Pharmacy and Pharmaceutical Sciences, 2012, University of Alberta

 Identification and quantification of pathogenic bacteria has become one of the key elements in biodefense, food safety, diagnostic and drug discovery. The aim of the… (more)

Subjects/Keywords: Peptide-immobilizatios; Leucocin A; Peptide-bacteria Interactions; Antimicrobial Peptides; Leucocin A; Peptide-Immobilization; Peptide-bacteria Interactions; Antimicrobial Peptides

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APA (6th Edition):

Etayash, H. R. (2012). Engineering Surface-tethered Bacteriocins for Studying Peptide-bacteria Interactions. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/5q47rq047

Chicago Manual of Style (16th Edition):

Etayash, Hashem Ra. “Engineering Surface-tethered Bacteriocins for Studying Peptide-bacteria Interactions.” 2012. Masters Thesis, University of Alberta. Accessed November 26, 2020. https://era.library.ualberta.ca/files/5q47rq047.

MLA Handbook (7th Edition):

Etayash, Hashem Ra. “Engineering Surface-tethered Bacteriocins for Studying Peptide-bacteria Interactions.” 2012. Web. 26 Nov 2020.

Vancouver:

Etayash HR. Engineering Surface-tethered Bacteriocins for Studying Peptide-bacteria Interactions. [Internet] [Masters thesis]. University of Alberta; 2012. [cited 2020 Nov 26]. Available from: https://era.library.ualberta.ca/files/5q47rq047.

Council of Science Editors:

Etayash HR. Engineering Surface-tethered Bacteriocins for Studying Peptide-bacteria Interactions. [Masters Thesis]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/5q47rq047


Universiteit Utrecht

25. Tjong, C.T.F. Immobilization strategies for peptide microarrrays.

Degree: 2012, Universiteit Utrecht

Peptide microarrays have been developed over the last decade into a technology that can profile biomolecules. It has proven to be a versatile tool for… (more)

Subjects/Keywords: Immobilization strategies; Peptide Microarrays; Peptides

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APA (6th Edition):

Tjong, C. T. F. (2012). Immobilization strategies for peptide microarrrays. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/256506

Chicago Manual of Style (16th Edition):

Tjong, C T F. “Immobilization strategies for peptide microarrrays.” 2012. Masters Thesis, Universiteit Utrecht. Accessed November 26, 2020. http://dspace.library.uu.nl:8080/handle/1874/256506.

MLA Handbook (7th Edition):

Tjong, C T F. “Immobilization strategies for peptide microarrrays.” 2012. Web. 26 Nov 2020.

Vancouver:

Tjong CTF. Immobilization strategies for peptide microarrrays. [Internet] [Masters thesis]. Universiteit Utrecht; 2012. [cited 2020 Nov 26]. Available from: http://dspace.library.uu.nl:8080/handle/1874/256506.

Council of Science Editors:

Tjong CTF. Immobilization strategies for peptide microarrrays. [Masters Thesis]. Universiteit Utrecht; 2012. Available from: http://dspace.library.uu.nl:8080/handle/1874/256506


Mississippi State University

26. Gyamfi, Hawa. Understanding binding-induced conformational change in the Pin1 Prolyl Isomerase.

Degree: MS, Chemistry, 2013, Mississippi State University

  Pin1 is a Prolyl Isomerase that catalyzes cis-trans isomerization of peptides with pSer/Thr-Pro motifs in many cell signaling proteins. This conformational switch is implicated… (more)

Subjects/Keywords: Pin1; Phospho-peptide; 15NTROSY; 15NRelaxation

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APA (6th Edition):

Gyamfi, H. (2013). Understanding binding-induced conformational change in the Pin1 Prolyl Isomerase. (Masters Thesis). Mississippi State University. Retrieved from http://sun.library.msstate.edu/ETD-db/theses/available/etd-10302013-204949/ ;

Chicago Manual of Style (16th Edition):

Gyamfi, Hawa. “Understanding binding-induced conformational change in the Pin1 Prolyl Isomerase.” 2013. Masters Thesis, Mississippi State University. Accessed November 26, 2020. http://sun.library.msstate.edu/ETD-db/theses/available/etd-10302013-204949/ ;.

MLA Handbook (7th Edition):

Gyamfi, Hawa. “Understanding binding-induced conformational change in the Pin1 Prolyl Isomerase.” 2013. Web. 26 Nov 2020.

Vancouver:

Gyamfi H. Understanding binding-induced conformational change in the Pin1 Prolyl Isomerase. [Internet] [Masters thesis]. Mississippi State University; 2013. [cited 2020 Nov 26]. Available from: http://sun.library.msstate.edu/ETD-db/theses/available/etd-10302013-204949/ ;.

Council of Science Editors:

Gyamfi H. Understanding binding-induced conformational change in the Pin1 Prolyl Isomerase. [Masters Thesis]. Mississippi State University; 2013. Available from: http://sun.library.msstate.edu/ETD-db/theses/available/etd-10302013-204949/ ;


University of Alberta

27. Binazadeh, Mojtaba. Effect of Secondary Structure on Surface Adsorption of Peptides.

Degree: PhD, Department of Chemical and Materials Engineering, 2013, University of Alberta

 Protein adsorption at the biomaterial-tissue interface has several detrimental consequences which undermines the widespread application of engineered materials. Herein, it was asked what role protein… (more)

Subjects/Keywords: Peptide; Surface Adsorption; Secondary Structure

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APA (6th Edition):

Binazadeh, M. (2013). Effect of Secondary Structure on Surface Adsorption of Peptides. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/jh343v004

Chicago Manual of Style (16th Edition):

Binazadeh, Mojtaba. “Effect of Secondary Structure on Surface Adsorption of Peptides.” 2013. Doctoral Dissertation, University of Alberta. Accessed November 26, 2020. https://era.library.ualberta.ca/files/jh343v004.

MLA Handbook (7th Edition):

Binazadeh, Mojtaba. “Effect of Secondary Structure on Surface Adsorption of Peptides.” 2013. Web. 26 Nov 2020.

Vancouver:

Binazadeh M. Effect of Secondary Structure on Surface Adsorption of Peptides. [Internet] [Doctoral dissertation]. University of Alberta; 2013. [cited 2020 Nov 26]. Available from: https://era.library.ualberta.ca/files/jh343v004.

Council of Science Editors:

Binazadeh M. Effect of Secondary Structure on Surface Adsorption of Peptides. [Doctoral Dissertation]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/jh343v004


University of Alberta

28. Shahin, Mostafa H. Development of polymer and lipid based nano-delivery systems for targeted cancer chemotherapy.

Degree: PhD, Faculty of Pharmacy and Pharmaceutical Sciences, 2012, University of Alberta

 Conventional chemotherapy agents can kill tumor cells and inhibit tumor growth, but they produce severe side effects on normal cells at the same time. To… (more)

Subjects/Keywords: peptide; liposomes; chemotherapy; polymeric micelle

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APA (6th Edition):

Shahin, M. H. (2012). Development of polymer and lipid based nano-delivery systems for targeted cancer chemotherapy. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/k0698856b

Chicago Manual of Style (16th Edition):

Shahin, Mostafa H. “Development of polymer and lipid based nano-delivery systems for targeted cancer chemotherapy.” 2012. Doctoral Dissertation, University of Alberta. Accessed November 26, 2020. https://era.library.ualberta.ca/files/k0698856b.

MLA Handbook (7th Edition):

Shahin, Mostafa H. “Development of polymer and lipid based nano-delivery systems for targeted cancer chemotherapy.” 2012. Web. 26 Nov 2020.

Vancouver:

Shahin MH. Development of polymer and lipid based nano-delivery systems for targeted cancer chemotherapy. [Internet] [Doctoral dissertation]. University of Alberta; 2012. [cited 2020 Nov 26]. Available from: https://era.library.ualberta.ca/files/k0698856b.

Council of Science Editors:

Shahin MH. Development of polymer and lipid based nano-delivery systems for targeted cancer chemotherapy. [Doctoral Dissertation]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/k0698856b


University of Alberta

29. Bodapati, Krishna Chaitanya. Synthesis and SAR studies of antimicrobial peptide Leucocin A.

Degree: MS, Faculty of Pharmacy and Pharmaceutical Sciences, 2011, University of Alberta

 In this study, we report the synthesis of a potent antimicrobial peptide Leucocin A (LeuA) using two solid phase peptide synthesis methods. One of the… (more)

Subjects/Keywords: antimicrobial peptide, leucocin a, bacteriocin

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APA (6th Edition):

Bodapati, K. C. (2011). Synthesis and SAR studies of antimicrobial peptide Leucocin A. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/cc08hg66t

Chicago Manual of Style (16th Edition):

Bodapati, Krishna Chaitanya. “Synthesis and SAR studies of antimicrobial peptide Leucocin A.” 2011. Masters Thesis, University of Alberta. Accessed November 26, 2020. https://era.library.ualberta.ca/files/cc08hg66t.

MLA Handbook (7th Edition):

Bodapati, Krishna Chaitanya. “Synthesis and SAR studies of antimicrobial peptide Leucocin A.” 2011. Web. 26 Nov 2020.

Vancouver:

Bodapati KC. Synthesis and SAR studies of antimicrobial peptide Leucocin A. [Internet] [Masters thesis]. University of Alberta; 2011. [cited 2020 Nov 26]. Available from: https://era.library.ualberta.ca/files/cc08hg66t.

Council of Science Editors:

Bodapati KC. Synthesis and SAR studies of antimicrobial peptide Leucocin A. [Masters Thesis]. University of Alberta; 2011. Available from: https://era.library.ualberta.ca/files/cc08hg66t


University of Manchester

30. Forbes, Sarah. Assessment of Apolipoprotein E Derived Peptides as Novel Antimicrobials for the Coating of Biomedical Devices.

Degree: 2013, University of Manchester

 The microbial contamination of biomedical devices is a leading cause of hospital- acquired infection. A number of strategies aimed at developing device coatings that are… (more)

Subjects/Keywords: Biocide; Antimicrobial peptide; Medical device

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APA (6th Edition):

Forbes, S. (2013). Assessment of Apolipoprotein E Derived Peptides as Novel Antimicrobials for the Coating of Biomedical Devices. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:185610

Chicago Manual of Style (16th Edition):

Forbes, Sarah. “Assessment of Apolipoprotein E Derived Peptides as Novel Antimicrobials for the Coating of Biomedical Devices.” 2013. Doctoral Dissertation, University of Manchester. Accessed November 26, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:185610.

MLA Handbook (7th Edition):

Forbes, Sarah. “Assessment of Apolipoprotein E Derived Peptides as Novel Antimicrobials for the Coating of Biomedical Devices.” 2013. Web. 26 Nov 2020.

Vancouver:

Forbes S. Assessment of Apolipoprotein E Derived Peptides as Novel Antimicrobials for the Coating of Biomedical Devices. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2020 Nov 26]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:185610.

Council of Science Editors:

Forbes S. Assessment of Apolipoprotein E Derived Peptides as Novel Antimicrobials for the Coating of Biomedical Devices. [Doctoral Dissertation]. University of Manchester; 2013. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:185610

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