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You searched for subject:(peptide). Showing records 1 – 30 of 2882 total matches.

[1] [2] [3] [4] [5] … [97]

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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 September 19, 2019. http://hdl.handle.net/11299/185633.

MLA Handbook (7th Edition):

Scott, Carolyn. “Peptide-functionalized hydrogels for three-dimensional cell culture.” 2016. Web. 19 Sep 2019.

Vancouver:

Scott C. Peptide-functionalized hydrogels for three-dimensional cell culture. [Internet] [Doctoral dissertation]. University of Minnesota; 2016. [cited 2019 Sep 19]. 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


University of Georgia

2. Walker, Jennifer Renee. Improving the stability of bioactive peptides using protein-based motifs.

Degree: PhD, Microbiology, 2002, University of Georgia

Peptide instability and poor delivery in humans hinders the development of effective peptide drugs. To search for novel protective motifs for stabilizing peptides, an in… (more)

Subjects/Keywords: peptide

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APA (6th Edition):

Walker, J. R. (2002). Improving the stability of bioactive peptides using protein-based motifs. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/walker_jennifer_r_200212_phd

Chicago Manual of Style (16th Edition):

Walker, Jennifer Renee. “Improving the stability of bioactive peptides using protein-based motifs.” 2002. Doctoral Dissertation, University of Georgia. Accessed September 19, 2019. http://purl.galileo.usg.edu/uga_etd/walker_jennifer_r_200212_phd.

MLA Handbook (7th Edition):

Walker, Jennifer Renee. “Improving the stability of bioactive peptides using protein-based motifs.” 2002. Web. 19 Sep 2019.

Vancouver:

Walker JR. Improving the stability of bioactive peptides using protein-based motifs. [Internet] [Doctoral dissertation]. University of Georgia; 2002. [cited 2019 Sep 19]. Available from: http://purl.galileo.usg.edu/uga_etd/walker_jennifer_r_200212_phd.

Council of Science Editors:

Walker JR. Improving the stability of bioactive peptides using protein-based motifs. [Doctoral Dissertation]. University of Georgia; 2002. Available from: http://purl.galileo.usg.edu/uga_etd/walker_jennifer_r_200212_phd


University of Georgia

3. Warren, James Walter. A molecular genetic approach to stabilizing bioactive peptides via protein-based motifs.

Degree: PhD, Microbiology, 2004, University of Georgia

 Instability of bioactive peptides represents a major challenge to the development of these molecules as drugs. The purpose of this study was the investigation of… (more)

Subjects/Keywords: Peptide

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APA (6th Edition):

Warren, J. W. (2004). A molecular genetic approach to stabilizing bioactive peptides via protein-based motifs. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/warren_james_w_200408_phd

Chicago Manual of Style (16th Edition):

Warren, James Walter. “A molecular genetic approach to stabilizing bioactive peptides via protein-based motifs.” 2004. Doctoral Dissertation, University of Georgia. Accessed September 19, 2019. http://purl.galileo.usg.edu/uga_etd/warren_james_w_200408_phd.

MLA Handbook (7th Edition):

Warren, James Walter. “A molecular genetic approach to stabilizing bioactive peptides via protein-based motifs.” 2004. Web. 19 Sep 2019.

Vancouver:

Warren JW. A molecular genetic approach to stabilizing bioactive peptides via protein-based motifs. [Internet] [Doctoral dissertation]. University of Georgia; 2004. [cited 2019 Sep 19]. Available from: http://purl.galileo.usg.edu/uga_etd/warren_james_w_200408_phd.

Council of Science Editors:

Warren JW. A molecular genetic approach to stabilizing bioactive peptides via protein-based motifs. [Doctoral Dissertation]. University of Georgia; 2004. Available from: http://purl.galileo.usg.edu/uga_etd/warren_james_w_200408_phd

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 September 19, 2019. 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. 19 Sep 2019.

Vancouver:

Cabalteja CC. Bioengineering alpha conotoxin ViI : from disulfide bonds to native chemical ligation. [Internet] [Thesis]. University of Hawaii – Manoa; 2015. [cited 2019 Sep 19]. 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 Hong Kong

5. 鲁尧; Lu, Yao. The study of cytotoxicity and membrane interaction of D-LAK antimicrobial peptides.

Degree: Master of Medical Sciences, 2015, University of Hong Kong

Tuberculosis (TB) remains a major global heath problem. Mismanagement of TB leads to the development of multidrug-resistant tuberculosis (MDR-TB). There is an urgent need to… (more)

Subjects/Keywords: Peptide antibiotics

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APA (6th Edition):

鲁尧; Lu, Y. (2015). The study of cytotoxicity and membrane interaction of D-LAK antimicrobial peptides. (Masters Thesis). University of Hong Kong. Retrieved from Lu, Y. [鲁尧]. (2015). The study of cytotoxicity and membrane interaction of D-LAK antimicrobial peptides. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5635922 ; http://hdl.handle.net/10722/221472

Chicago Manual of Style (16th Edition):

鲁尧; Lu, Yao. “The study of cytotoxicity and membrane interaction of D-LAK antimicrobial peptides.” 2015. Masters Thesis, University of Hong Kong. Accessed September 19, 2019. Lu, Y. [鲁尧]. (2015). The study of cytotoxicity and membrane interaction of D-LAK antimicrobial peptides. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5635922 ; http://hdl.handle.net/10722/221472.

MLA Handbook (7th Edition):

鲁尧; Lu, Yao. “The study of cytotoxicity and membrane interaction of D-LAK antimicrobial peptides.” 2015. Web. 19 Sep 2019.

Vancouver:

鲁尧; Lu Y. The study of cytotoxicity and membrane interaction of D-LAK antimicrobial peptides. [Internet] [Masters thesis]. University of Hong Kong; 2015. [cited 2019 Sep 19]. Available from: Lu, Y. [鲁尧]. (2015). The study of cytotoxicity and membrane interaction of D-LAK antimicrobial peptides. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5635922 ; http://hdl.handle.net/10722/221472.

Council of Science Editors:

鲁尧; Lu Y. The study of cytotoxicity and membrane interaction of D-LAK antimicrobial peptides. [Masters Thesis]. University of Hong Kong; 2015. Available from: Lu, Y. [鲁尧]. (2015). The study of cytotoxicity and membrane interaction of D-LAK antimicrobial peptides. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5635922 ; http://hdl.handle.net/10722/221472


Wake Forest University

6. 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 September 19, 2019. 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. 19 Sep 2019.

Vancouver:

Altamimi AM. TESTING THE EFFECT OF A NOVEL HYDROGEN SULFIDE RELEASING PEPTIDE ON INFECTED BURN WOUNDS. [Internet] [Thesis]. Wake Forest University; 2019. [cited 2019 Sep 19]. 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

7. 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 September 19, 2019. 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. 19 Sep 2019.

Vancouver:

Montandon C. Identification and characterization of putative Toc159 interacting partners. [Internet] [Thesis]. Université de Neuchâtel; 2015. [cited 2019 Sep 19]. 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


University of Sydney

8. 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 September 19, 2019. 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. 19 Sep 2019.

Vancouver:

Wang X. Development and Application of Novel Methods for the Synthesis of Modified Proteins . [Internet] [Thesis]. University of Sydney; 2018. [cited 2019 Sep 19]. 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

9. 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 September 19, 2019. 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. 19 Sep 2019.

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 2019 Sep 19]. 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


Brigham Young University

10. Dallon, Emma Kay. Exploration of Antimicrobial Activity in Natural Peptides and High-Throughput Discovery of Synthetic Peptides.

Degree: MS, 2018, Brigham Young University

 Despite many medical advances, antibiotic resistant bacteria increasingly plague the modern world, necessitating discovery of new antibiotics. One area of nature that can provide inspiration… (more)

Subjects/Keywords: antimicrobial peptide; NCR peptide; Life Sciences

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APA (6th Edition):

Dallon, E. K. (2018). Exploration of Antimicrobial Activity in Natural Peptides and High-Throughput Discovery of Synthetic Peptides. (Masters Thesis). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=8468&context=etd

Chicago Manual of Style (16th Edition):

Dallon, Emma Kay. “Exploration of Antimicrobial Activity in Natural Peptides and High-Throughput Discovery of Synthetic Peptides.” 2018. Masters Thesis, Brigham Young University. Accessed September 19, 2019. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=8468&context=etd.

MLA Handbook (7th Edition):

Dallon, Emma Kay. “Exploration of Antimicrobial Activity in Natural Peptides and High-Throughput Discovery of Synthetic Peptides.” 2018. Web. 19 Sep 2019.

Vancouver:

Dallon EK. Exploration of Antimicrobial Activity in Natural Peptides and High-Throughput Discovery of Synthetic Peptides. [Internet] [Masters thesis]. Brigham Young University; 2018. [cited 2019 Sep 19]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=8468&context=etd.

Council of Science Editors:

Dallon EK. Exploration of Antimicrobial Activity in Natural Peptides and High-Throughput Discovery of Synthetic Peptides. [Masters Thesis]. Brigham Young University; 2018. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=8468&context=etd


University of Georgia

11. Haley, Jennifer Ayers. Polymer-peptide hybrids: self-assembly and combinative assembly with DNA.

Degree: PhD, Chemistry, 2011, University of Georgia

 Polymer-Peptide hybrids are a novel class of macromolecules that combine sophisticated functionality of biopolymers with synthetic versatility of synthetic polymers. Initially developed by biochemist for… (more)

Subjects/Keywords: Polymer-Peptide Hybrids

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APA (6th Edition):

Haley, J. A. (2011). Polymer-peptide hybrids: self-assembly and combinative assembly with DNA. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/haley_jennifer_a_201105_phd

Chicago Manual of Style (16th Edition):

Haley, Jennifer Ayers. “Polymer-peptide hybrids: self-assembly and combinative assembly with DNA.” 2011. Doctoral Dissertation, University of Georgia. Accessed September 19, 2019. http://purl.galileo.usg.edu/uga_etd/haley_jennifer_a_201105_phd.

MLA Handbook (7th Edition):

Haley, Jennifer Ayers. “Polymer-peptide hybrids: self-assembly and combinative assembly with DNA.” 2011. Web. 19 Sep 2019.

Vancouver:

Haley JA. Polymer-peptide hybrids: self-assembly and combinative assembly with DNA. [Internet] [Doctoral dissertation]. University of Georgia; 2011. [cited 2019 Sep 19]. Available from: http://purl.galileo.usg.edu/uga_etd/haley_jennifer_a_201105_phd.

Council of Science Editors:

Haley JA. Polymer-peptide hybrids: self-assembly and combinative assembly with DNA. [Doctoral Dissertation]. University of Georgia; 2011. Available from: http://purl.galileo.usg.edu/uga_etd/haley_jennifer_a_201105_phd


University of Alberta

12. 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 September 19, 2019. https://era.library.ualberta.ca/files/8g84mn557.

MLA Handbook (7th Edition):

Lohans, Christopher T. “Structural Characterization of Bacterial Antimicrobial Peptides.” 2014. Web. 19 Sep 2019.

Vancouver:

Lohans CT. Structural Characterization of Bacterial Antimicrobial Peptides. [Internet] [Doctoral dissertation]. University of Alberta; 2014. [cited 2019 Sep 19]. 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


Mahatma Gandhi University

13. 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 September 19, 2019. 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. 19 Sep 2019.

Vancouver:

Sasikumar PG. Solid phase peptide synthesis using glycerol based cross linked polymer supports. [Internet] [Thesis]. Mahatma Gandhi University; 2010. [cited 2019 Sep 19]. 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


University of Aberdeen

14. Carnapete Alves Meneses, Célia Clarisse. The development of a facile solution-phase method for the synthesis of peptides.

Degree: 2010, University of Aberdeen

 The synthesis of peptides can be considered as the rate-limiting step in the development of peptide-based medicines. Synthetic methods currently available are limited by several… (more)

Subjects/Keywords: 547.7; Peptide synthesis

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APA (6th Edition):

Carnapete Alves Meneses, C. C. (2010). The development of a facile solution-phase method for the synthesis of peptides. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=166204 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.540483

Chicago Manual of Style (16th Edition):

Carnapete Alves Meneses, Célia Clarisse. “The development of a facile solution-phase method for the synthesis of peptides.” 2010. Doctoral Dissertation, University of Aberdeen. Accessed September 19, 2019. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=166204 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.540483.

MLA Handbook (7th Edition):

Carnapete Alves Meneses, Célia Clarisse. “The development of a facile solution-phase method for the synthesis of peptides.” 2010. Web. 19 Sep 2019.

Vancouver:

Carnapete Alves Meneses CC. The development of a facile solution-phase method for the synthesis of peptides. [Internet] [Doctoral dissertation]. University of Aberdeen; 2010. [cited 2019 Sep 19]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=166204 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.540483.

Council of Science Editors:

Carnapete Alves Meneses CC. The development of a facile solution-phase method for the synthesis of peptides. [Doctoral Dissertation]. University of Aberdeen; 2010. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=166204 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.540483

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

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 September 19, 2019. 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. 19 Sep 2019.

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 2019 Sep 19]. 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 Manchester

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

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 September 19, 2019. 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. 19 Sep 2019.

Vancouver:

Wu M. Bio-engineering of Antibiotic Enduracidin Biosynthetic Pathways and PreQ1 Riboswitch. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2019 Sep 19]. 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


University of Manchester

17. 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 September 19, 2019. 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. 19 Sep 2019.

Vancouver:

Szkolar L. The Development of Functional Peptide Scaffolds for Cell Culture. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Sep 19]. 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


Tulane University

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

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 September 19, 2019. 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. 19 Sep 2019.

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 2019 Sep 19]. 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


University of New South Wales

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

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 September 19, 2019. 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. 19 Sep 2019.

Vancouver:

Wang Z. RGD peptide derivatives as tools for tumour imaging and therapy. [Internet] [Masters thesis]. University of New South Wales; 2013. [cited 2019 Sep 19]. 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

20. 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 September 19, 2019. http://hdl.handle.net/1842/9605.

MLA Handbook (7th Edition):

Svensen, Nina. “Cellular analysis and PNA encoded libraries.” 2011. Web. 19 Sep 2019.

Vancouver:

Svensen N. Cellular analysis and PNA encoded libraries. [Internet] [Doctoral dissertation]. University of Edinburgh; 2011. [cited 2019 Sep 19]. 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 Illinois – Chicago

21. 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 September 19, 2019. 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. 19 Sep 2019.

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 2019 Sep 19]. 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


University of Manchester

22. Wu, Ming-Cheng. Bio-engineering of antibiotic enduracidin biosynthetic pathways and PreQ1 riboswitch.

Degree: PhD, 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: 572; non-ribosomal peptide

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

APA (6th Edition):

Wu, M. (2011). Bio-engineering of antibiotic enduracidin biosynthetic pathways and PreQ1 riboswitch. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/bioengineering-of-antibiotic-enduracidin-biosynthetic-pathways-and-preq1-riboswitch(5eb04bf7-f20b-49d0-96f6-cd06f92676d1).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.701088

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 September 19, 2019. https://www.research.manchester.ac.uk/portal/en/theses/bioengineering-of-antibiotic-enduracidin-biosynthetic-pathways-and-preq1-riboswitch(5eb04bf7-f20b-49d0-96f6-cd06f92676d1).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.701088.

MLA Handbook (7th Edition):

Wu, Ming-Cheng. “Bio-engineering of antibiotic enduracidin biosynthetic pathways and PreQ1 riboswitch.” 2011. Web. 19 Sep 2019.

Vancouver:

Wu M. Bio-engineering of antibiotic enduracidin biosynthetic pathways and PreQ1 riboswitch. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2019 Sep 19]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/bioengineering-of-antibiotic-enduracidin-biosynthetic-pathways-and-preq1-riboswitch(5eb04bf7-f20b-49d0-96f6-cd06f92676d1).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.701088.

Council of Science Editors:

Wu M. Bio-engineering of antibiotic enduracidin biosynthetic pathways and PreQ1 riboswitch. [Doctoral Dissertation]. University of Manchester; 2011. Available from: https://www.research.manchester.ac.uk/portal/en/theses/bioengineering-of-antibiotic-enduracidin-biosynthetic-pathways-and-preq1-riboswitch(5eb04bf7-f20b-49d0-96f6-cd06f92676d1).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.701088


University of Alberta

23. 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 September 19, 2019. https://era.library.ualberta.ca/files/jh343v004.

MLA Handbook (7th Edition):

Binazadeh, Mojtaba. “Effect of Secondary Structure on Surface Adsorption of Peptides.” 2013. Web. 19 Sep 2019.

Vancouver:

Binazadeh M. Effect of Secondary Structure on Surface Adsorption of Peptides. [Internet] [Doctoral dissertation]. University of Alberta; 2013. [cited 2019 Sep 19]. 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

24. 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 September 19, 2019. 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. 19 Sep 2019.

Vancouver:

Shahin MH. Development of polymer and lipid based nano-delivery systems for targeted cancer chemotherapy. [Internet] [Doctoral dissertation]. University of Alberta; 2012. [cited 2019 Sep 19]. 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

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

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 September 19, 2019. 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. 19 Sep 2019.

Vancouver:

Bodapati KC. Synthesis and SAR studies of antimicrobial peptide Leucocin A. [Internet] [Masters thesis]. University of Alberta; 2011. [cited 2019 Sep 19]. 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 KwaZulu-Natal

26. [No author]. Synthesis and aggregation dynamics of amylin.

Degree: Biochemistry, 2013, University of KwaZulu-Natal

 Amylin is a 37 amino acid long peptide that aggregates into toxic oligomers and fibrils. Since amylin is secreted by and also acts on pancreatic… (more)

Subjects/Keywords: Amylin.; Peptide hormones.; Amyloid.; Biochemistry.

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APA (6th Edition):

author], [. (2013). Synthesis and aggregation dynamics of amylin. (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/10076

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):

author], [No. “Synthesis and aggregation dynamics of amylin. ” 2013. Thesis, University of KwaZulu-Natal. Accessed September 19, 2019. http://hdl.handle.net/10413/10076.

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

MLA Handbook (7th Edition):

author], [No. “Synthesis and aggregation dynamics of amylin. ” 2013. Web. 19 Sep 2019.

Vancouver:

author] [. Synthesis and aggregation dynamics of amylin. [Internet] [Thesis]. University of KwaZulu-Natal; 2013. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/10413/10076.

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

Council of Science Editors:

author] [. Synthesis and aggregation dynamics of amylin. [Thesis]. University of KwaZulu-Natal; 2013. Available from: http://hdl.handle.net/10413/10076

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

27. Singh, Gurpreet. Molecular simulation studies of peptide aggregation in small finite sized systems and near surfaces.

Degree: 2009, Technische Universität Dortmund

 Die Aggregation von Proteinen spielt in verschiedenen biologischen Prozessen eine Rolle und wird insbesondere mit vielen Krankheiten wie Alzheimer, Parkinson oder Type II Diabetes Mellitus… (more)

Subjects/Keywords: Molecular simulation; Peptide aggregation; 540

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APA (6th Edition):

Singh, G. (2009). Molecular simulation studies of peptide aggregation in small finite sized systems and near surfaces. (Thesis). Technische Universität Dortmund. Retrieved from http://hdl.handle.net/2003/26021

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):

Singh, Gurpreet. “Molecular simulation studies of peptide aggregation in small finite sized systems and near surfaces.” 2009. Thesis, Technische Universität Dortmund. Accessed September 19, 2019. http://hdl.handle.net/2003/26021.

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

MLA Handbook (7th Edition):

Singh, Gurpreet. “Molecular simulation studies of peptide aggregation in small finite sized systems and near surfaces.” 2009. Web. 19 Sep 2019.

Vancouver:

Singh G. Molecular simulation studies of peptide aggregation in small finite sized systems and near surfaces. [Internet] [Thesis]. Technische Universität Dortmund; 2009. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/2003/26021.

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

Council of Science Editors:

Singh G. Molecular simulation studies of peptide aggregation in small finite sized systems and near surfaces. [Thesis]. Technische Universität Dortmund; 2009. Available from: http://hdl.handle.net/2003/26021

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


NSYSU

28. 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 September 19, 2019. 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. 19 Sep 2019.

Vancouver:

Huang H. Influence of chemical conditions on human insulin fibril structure. [Internet] [Thesis]. NSYSU; 2013. [cited 2019 Sep 19]. 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


University of Akron

29. Liu, Qianhui. Structure-Property Relationship of "Peptide-like" Polyesters.

Degree: MS, Polymer Science, 2015, University of Akron

 Polyesters are wildly used materials in biomedical field such as drug delivery material, tissue engineering scaffolds material such as for bone regeneration and so on.… (more)

Subjects/Keywords: Polymers; polyesters, peptide-like, structures

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

APA (6th Edition):

Liu, Q. (2015). Structure-Property Relationship of "Peptide-like" Polyesters. (Masters Thesis). University of Akron. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=akron1428336910

Chicago Manual of Style (16th Edition):

Liu, Qianhui. “Structure-Property Relationship of "Peptide-like" Polyesters.” 2015. Masters Thesis, University of Akron. Accessed September 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=akron1428336910.

MLA Handbook (7th Edition):

Liu, Qianhui. “Structure-Property Relationship of "Peptide-like" Polyesters.” 2015. Web. 19 Sep 2019.

Vancouver:

Liu Q. Structure-Property Relationship of "Peptide-like" Polyesters. [Internet] [Masters thesis]. University of Akron; 2015. [cited 2019 Sep 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron1428336910.

Council of Science Editors:

Liu Q. Structure-Property Relationship of "Peptide-like" Polyesters. [Masters Thesis]. University of Akron; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron1428336910


Ruhr Universität Bochum

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

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 September 19, 2019. 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. 19 Sep 2019.

Vancouver:

Penkova M. Arginine and Tryptophan rich antimicrobial peptides (AMPs) : modifications, application and mode of action. [Internet] [Thesis]. Ruhr Universität Bochum; 2010. [cited 2019 Sep 19]. 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

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