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You searched for subject:(Vaccine development). Showing records 1 – 30 of 61 total matches.

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University of Sheffield

1. Wright, Lynda J. Identification and characterisation of components expressed by gram-positive bacterial pathogens during human infection.

Degree: PhD, 2008, University of Sheffield

Gram-positive pathogens are responsible for a wide range of global diseases, including nosocomial infections. The increasing incidence of antibiotic-resistant strains warrants the development of novel therapeutic strategies to combat these organisms.

Subjects/Keywords: 616.929061; Streptococcal infections, Staphylococcal infections, Vaccine development

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APA (6th Edition):

Wright, L. J. (2008). Identification and characterisation of components expressed by gram-positive bacterial pathogens during human infection. (Doctoral Dissertation). University of Sheffield. Retrieved from http://etheses.whiterose.ac.uk/10312/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.489062

Chicago Manual of Style (16th Edition):

Wright, Lynda J. “Identification and characterisation of components expressed by gram-positive bacterial pathogens during human infection.” 2008. Doctoral Dissertation, University of Sheffield. Accessed June 25, 2019. http://etheses.whiterose.ac.uk/10312/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.489062.

MLA Handbook (7th Edition):

Wright, Lynda J. “Identification and characterisation of components expressed by gram-positive bacterial pathogens during human infection.” 2008. Web. 25 Jun 2019.

Vancouver:

Wright LJ. Identification and characterisation of components expressed by gram-positive bacterial pathogens during human infection. [Internet] [Doctoral dissertation]. University of Sheffield; 2008. [cited 2019 Jun 25]. Available from: http://etheses.whiterose.ac.uk/10312/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.489062.

Council of Science Editors:

Wright LJ. Identification and characterisation of components expressed by gram-positive bacterial pathogens during human infection. [Doctoral Dissertation]. University of Sheffield; 2008. Available from: http://etheses.whiterose.ac.uk/10312/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.489062


Massey University

2. Sattar, Sadia. Filamentous phage-derived nano-rods for applications in diagnostics and vaccines.

Degree: PhD, Biochemistry, 2013, Massey University

 Filamentous bacteriophage, as their name indicates are filament-like bacterial viruses. The F-pilus-specific filamentous phage of Escherichia coli, Ff (f1, M13 and fd) are resistant to… (more)

Subjects/Keywords: Bacteriophages; Biotechnology; Vaccine development; Diagnostics; Nanobiotechnology

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APA (6th Edition):

Sattar, S. (2013). Filamentous phage-derived nano-rods for applications in diagnostics and vaccines. (Doctoral Dissertation). Massey University. Retrieved from http://hdl.handle.net/10179/5539

Chicago Manual of Style (16th Edition):

Sattar, Sadia. “Filamentous phage-derived nano-rods for applications in diagnostics and vaccines.” 2013. Doctoral Dissertation, Massey University. Accessed June 25, 2019. http://hdl.handle.net/10179/5539.

MLA Handbook (7th Edition):

Sattar, Sadia. “Filamentous phage-derived nano-rods for applications in diagnostics and vaccines.” 2013. Web. 25 Jun 2019.

Vancouver:

Sattar S. Filamentous phage-derived nano-rods for applications in diagnostics and vaccines. [Internet] [Doctoral dissertation]. Massey University; 2013. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10179/5539.

Council of Science Editors:

Sattar S. Filamentous phage-derived nano-rods for applications in diagnostics and vaccines. [Doctoral Dissertation]. Massey University; 2013. Available from: http://hdl.handle.net/10179/5539


Kansas State University

3. Tjernagel, Adam. Role and perceptions about communication: the case of new product development in the animal health industry.

Degree: Master of Agribusiness, Department of Agricultural Economics, 2018, Kansas State University

 The development of vaccines and similar pharmaceutical products in the animal health industry are expensive and follow very specific pathways to comply with regulatory requirements… (more)

Subjects/Keywords: Vaccine; Product development; Animal health; Communication

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APA (6th Edition):

Tjernagel, A. (2018). Role and perceptions about communication: the case of new product development in the animal health industry. (Masters Thesis). Kansas State University. Retrieved from http://hdl.handle.net/2097/38423

Chicago Manual of Style (16th Edition):

Tjernagel, Adam. “Role and perceptions about communication: the case of new product development in the animal health industry.” 2018. Masters Thesis, Kansas State University. Accessed June 25, 2019. http://hdl.handle.net/2097/38423.

MLA Handbook (7th Edition):

Tjernagel, Adam. “Role and perceptions about communication: the case of new product development in the animal health industry.” 2018. Web. 25 Jun 2019.

Vancouver:

Tjernagel A. Role and perceptions about communication: the case of new product development in the animal health industry. [Internet] [Masters thesis]. Kansas State University; 2018. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/2097/38423.

Council of Science Editors:

Tjernagel A. Role and perceptions about communication: the case of new product development in the animal health industry. [Masters Thesis]. Kansas State University; 2018. Available from: http://hdl.handle.net/2097/38423


University of Notre Dame

4. Amy M McHenry. Immunological characterization of the P. vivax DBP</h1>.

Degree: PhD, Biological Sciences, 2009, University of Notre Dame

  Plasmodium vivax is responsible for 70-80 million cases of malaria annually and has the widest geographical distribution of the human malaria parasites. Although not… (more)

Subjects/Keywords: polymorphisms; malaria; vaccine development; immune selection; Plasmodium

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APA (6th Edition):

McHenry, A. M. (2009). Immunological characterization of the P. vivax DBP</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/cz30pr78h8x

Chicago Manual of Style (16th Edition):

McHenry, Amy M. “Immunological characterization of the P. vivax DBP</h1>.” 2009. Doctoral Dissertation, University of Notre Dame. Accessed June 25, 2019. https://curate.nd.edu/show/cz30pr78h8x.

MLA Handbook (7th Edition):

McHenry, Amy M. “Immunological characterization of the P. vivax DBP</h1>.” 2009. Web. 25 Jun 2019.

Vancouver:

McHenry AM. Immunological characterization of the P. vivax DBP</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2009. [cited 2019 Jun 25]. Available from: https://curate.nd.edu/show/cz30pr78h8x.

Council of Science Editors:

McHenry AM. Immunological characterization of the P. vivax DBP</h1>. [Doctoral Dissertation]. University of Notre Dame; 2009. Available from: https://curate.nd.edu/show/cz30pr78h8x


University of Sydney

5. Nisa, Annuurun. Novel subunit and live vaccine strategies to protect against tuberculosis .

Degree: 2018, University of Sydney

 Tuberculosis (TB) has plagued human populations throughout much of known human history and now listed as one of the top ten causes of death worldwide.… (more)

Subjects/Keywords: Mycobacterium tuberculosis; Vaccine development; Mouse model

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APA (6th Edition):

Nisa, A. (2018). Novel subunit and live vaccine strategies to protect against tuberculosis . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/20467

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):

Nisa, Annuurun. “Novel subunit and live vaccine strategies to protect against tuberculosis .” 2018. Thesis, University of Sydney. Accessed June 25, 2019. http://hdl.handle.net/2123/20467.

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

MLA Handbook (7th Edition):

Nisa, Annuurun. “Novel subunit and live vaccine strategies to protect against tuberculosis .” 2018. Web. 25 Jun 2019.

Vancouver:

Nisa A. Novel subunit and live vaccine strategies to protect against tuberculosis . [Internet] [Thesis]. University of Sydney; 2018. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/2123/20467.

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

Council of Science Editors:

Nisa A. Novel subunit and live vaccine strategies to protect against tuberculosis . [Thesis]. University of Sydney; 2018. Available from: http://hdl.handle.net/2123/20467

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


University of Alberta

6. Waye, Arianna E. Essays in Applied Vaccine Economics.

Degree: PhD, Department of Medicine, 2013, University of Alberta

 Objectives: This thesis consists of 3 partial vaccine economic evaluations. The objectives were to: 1) estimate the effectiveness of Canada’s universal varicella childhood immunization strategy… (more)

Subjects/Keywords: Effectiveness; Cost; Economics; Varicella; Research and Development; Vaccine

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APA (6th Edition):

Waye, A. E. (2013). Essays in Applied Vaccine Economics. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/jq085m68b

Chicago Manual of Style (16th Edition):

Waye, Arianna E. “Essays in Applied Vaccine Economics.” 2013. Doctoral Dissertation, University of Alberta. Accessed June 25, 2019. https://era.library.ualberta.ca/files/jq085m68b.

MLA Handbook (7th Edition):

Waye, Arianna E. “Essays in Applied Vaccine Economics.” 2013. Web. 25 Jun 2019.

Vancouver:

Waye AE. Essays in Applied Vaccine Economics. [Internet] [Doctoral dissertation]. University of Alberta; 2013. [cited 2019 Jun 25]. Available from: https://era.library.ualberta.ca/files/jq085m68b.

Council of Science Editors:

Waye AE. Essays in Applied Vaccine Economics. [Doctoral Dissertation]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/jq085m68b


Universiteit Utrecht

7. Feenstra, F. Novel bluetongue vaccine platform : NS3/NS3a knockout virus as Disabled Infectious Single Animal (DISA) vaccine.

Degree: 2016, Universiteit Utrecht

 Bluetongue (BT) is a disease of ruminants caused by the bluetongue virus (BTV) transmitted by bites of Culicoides midges. Bluetongue has a worldwide prevalence and… (more)

Subjects/Keywords: Reoviridae; Orbivirus; Bluetongue; Reverse genetics; NS3; VP2; Serotype; Vaccine development; DIVA

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APA (6th Edition):

Feenstra, F. (2016). Novel bluetongue vaccine platform : NS3/NS3a knockout virus as Disabled Infectious Single Animal (DISA) vaccine. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/331177

Chicago Manual of Style (16th Edition):

Feenstra, F. “Novel bluetongue vaccine platform : NS3/NS3a knockout virus as Disabled Infectious Single Animal (DISA) vaccine.” 2016. Doctoral Dissertation, Universiteit Utrecht. Accessed June 25, 2019. http://dspace.library.uu.nl:8080/handle/1874/331177.

MLA Handbook (7th Edition):

Feenstra, F. “Novel bluetongue vaccine platform : NS3/NS3a knockout virus as Disabled Infectious Single Animal (DISA) vaccine.” 2016. Web. 25 Jun 2019.

Vancouver:

Feenstra F. Novel bluetongue vaccine platform : NS3/NS3a knockout virus as Disabled Infectious Single Animal (DISA) vaccine. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2016. [cited 2019 Jun 25]. Available from: http://dspace.library.uu.nl:8080/handle/1874/331177.

Council of Science Editors:

Feenstra F. Novel bluetongue vaccine platform : NS3/NS3a knockout virus as Disabled Infectious Single Animal (DISA) vaccine. [Doctoral Dissertation]. Universiteit Utrecht; 2016. Available from: http://dspace.library.uu.nl:8080/handle/1874/331177


University of Kansas

8. Iyer Gowrishankara, Vidyashankara. Preformulation Development of a monovalent recombinant-based subunit vaccine, a multivalent recombinant-based subunit vaccine and a multivalent live attenuated viral vaccine.

Degree: PhD, Bioengineering, 2012, University of Kansas

 The objective of this project is to explore of the use of the empirical phase diagram approach in the formulation development of several forms of… (more)

Subjects/Keywords: Pharmaceutical sciences; Adjuvants; Antigen; Development; Empirical phase diagram; Formulation; Vaccine

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APA (6th Edition):

Iyer Gowrishankara, V. (2012). Preformulation Development of a monovalent recombinant-based subunit vaccine, a multivalent recombinant-based subunit vaccine and a multivalent live attenuated viral vaccine. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/14832

Chicago Manual of Style (16th Edition):

Iyer Gowrishankara, Vidyashankara. “Preformulation Development of a monovalent recombinant-based subunit vaccine, a multivalent recombinant-based subunit vaccine and a multivalent live attenuated viral vaccine.” 2012. Doctoral Dissertation, University of Kansas. Accessed June 25, 2019. http://hdl.handle.net/1808/14832.

MLA Handbook (7th Edition):

Iyer Gowrishankara, Vidyashankara. “Preformulation Development of a monovalent recombinant-based subunit vaccine, a multivalent recombinant-based subunit vaccine and a multivalent live attenuated viral vaccine.” 2012. Web. 25 Jun 2019.

Vancouver:

Iyer Gowrishankara V. Preformulation Development of a monovalent recombinant-based subunit vaccine, a multivalent recombinant-based subunit vaccine and a multivalent live attenuated viral vaccine. [Internet] [Doctoral dissertation]. University of Kansas; 2012. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/1808/14832.

Council of Science Editors:

Iyer Gowrishankara V. Preformulation Development of a monovalent recombinant-based subunit vaccine, a multivalent recombinant-based subunit vaccine and a multivalent live attenuated viral vaccine. [Doctoral Dissertation]. University of Kansas; 2012. Available from: http://hdl.handle.net/1808/14832


University of Texas Medical Branch – Galveston

9. [No author]. Mechanisms of attenuation of the live Junin virus vaccine strain, Candid1 .

Degree: University of Texas Medical Branch – Galveston

 Millions of individuals are at risk of arenavirus infection worldwide, with untreated infections often resulting in potentially lethal disease. Junin virus (JUNV), the causative agent… (more)

Subjects/Keywords: Junin virus; vaccine development

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APA (6th Edition):

author], [. (n.d.). Mechanisms of attenuation of the live Junin virus vaccine strain, Candid1 . (Thesis). University of Texas Medical Branch – Galveston. Retrieved from http://hdl.handle.net/2152.3/10735

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

Chicago Manual of Style (16th Edition):

author], [No. “Mechanisms of attenuation of the live Junin virus vaccine strain, Candid1 .” Thesis, University of Texas Medical Branch – Galveston. Accessed June 25, 2019. http://hdl.handle.net/2152.3/10735.

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

MLA Handbook (7th Edition):

author], [No. “Mechanisms of attenuation of the live Junin virus vaccine strain, Candid1 .” Web. 25 Jun 2019.

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

Vancouver:

author] [. Mechanisms of attenuation of the live Junin virus vaccine strain, Candid1 . [Internet] [Thesis]. University of Texas Medical Branch – Galveston; [cited 2019 Jun 25]. Available from: http://hdl.handle.net/2152.3/10735.

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

Council of Science Editors:

author] [. Mechanisms of attenuation of the live Junin virus vaccine strain, Candid1 . [Thesis]. University of Texas Medical Branch – Galveston; Available from: http://hdl.handle.net/2152.3/10735

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


University of Southern California

10. Dai, Bingbing. Engineering viral vectors for T-cell immunotherapy and HIV-1 vaccine.

Degree: PhD, Materials Science, 2012, University of Southern California

 T cell immunotherapy fell into two categories: passive (adoptive) transfer of in vitro expanded cells, and active expansion of antigen-specific T cells by in vivo… (more)

Subjects/Keywords: gene delivery; HIV/AIDS vaccine; lentiviral vector engineering; stem cell development; PD1/PD1L pathway

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APA (6th Edition):

Dai, B. (2012). Engineering viral vectors for T-cell immunotherapy and HIV-1 vaccine. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/406/rec/2370

Chicago Manual of Style (16th Edition):

Dai, Bingbing. “Engineering viral vectors for T-cell immunotherapy and HIV-1 vaccine.” 2012. Doctoral Dissertation, University of Southern California. Accessed June 25, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/406/rec/2370.

MLA Handbook (7th Edition):

Dai, Bingbing. “Engineering viral vectors for T-cell immunotherapy and HIV-1 vaccine.” 2012. Web. 25 Jun 2019.

Vancouver:

Dai B. Engineering viral vectors for T-cell immunotherapy and HIV-1 vaccine. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2019 Jun 25]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/406/rec/2370.

Council of Science Editors:

Dai B. Engineering viral vectors for T-cell immunotherapy and HIV-1 vaccine. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/406/rec/2370


University of Surrey

11. Al-Zarouni, Mansour. Expression of recombinant antigen in BCG.

Degree: PhD, 2000, University of Surrey

 Little is known about the effect of different modes of expression of an antigen in rBCG on immune response. An appropriate wing of the immune… (more)

Subjects/Keywords: 579; Immune response; Vaccine development; Bacteria

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APA (6th Edition):

Al-Zarouni, M. (2000). Expression of recombinant antigen in BCG. (Doctoral Dissertation). University of Surrey. Retrieved from http://epubs.surrey.ac.uk/843308/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.326533

Chicago Manual of Style (16th Edition):

Al-Zarouni, Mansour. “Expression of recombinant antigen in BCG.” 2000. Doctoral Dissertation, University of Surrey. Accessed June 25, 2019. http://epubs.surrey.ac.uk/843308/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.326533.

MLA Handbook (7th Edition):

Al-Zarouni, Mansour. “Expression of recombinant antigen in BCG.” 2000. Web. 25 Jun 2019.

Vancouver:

Al-Zarouni M. Expression of recombinant antigen in BCG. [Internet] [Doctoral dissertation]. University of Surrey; 2000. [cited 2019 Jun 25]. Available from: http://epubs.surrey.ac.uk/843308/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.326533.

Council of Science Editors:

Al-Zarouni M. Expression of recombinant antigen in BCG. [Doctoral Dissertation]. University of Surrey; 2000. Available from: http://epubs.surrey.ac.uk/843308/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.326533


University of Plymouth

12. Hurley, Louise Margaret. Ichthyophthirius multifiliis Fouquet : development and assessment of in vitro systems for long term maintenance.

Degree: PhD, 1999, University of Plymouth

 Twelve isolates of Ichthyophthirius multifiliis were successfully established and maintained by serial passage through naïve carp, for a maximum of 39 laboratory cycles. The management… (more)

Subjects/Keywords: 639.8; Fish cell culture; Vaccine development; Infection

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APA (6th Edition):

Hurley, L. M. (1999). Ichthyophthirius multifiliis Fouquet : development and assessment of in vitro systems for long term maintenance. (Doctoral Dissertation). University of Plymouth. Retrieved from http://hdl.handle.net/10026.1/2526

Chicago Manual of Style (16th Edition):

Hurley, Louise Margaret. “Ichthyophthirius multifiliis Fouquet : development and assessment of in vitro systems for long term maintenance.” 1999. Doctoral Dissertation, University of Plymouth. Accessed June 25, 2019. http://hdl.handle.net/10026.1/2526.

MLA Handbook (7th Edition):

Hurley, Louise Margaret. “Ichthyophthirius multifiliis Fouquet : development and assessment of in vitro systems for long term maintenance.” 1999. Web. 25 Jun 2019.

Vancouver:

Hurley LM. Ichthyophthirius multifiliis Fouquet : development and assessment of in vitro systems for long term maintenance. [Internet] [Doctoral dissertation]. University of Plymouth; 1999. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10026.1/2526.

Council of Science Editors:

Hurley LM. Ichthyophthirius multifiliis Fouquet : development and assessment of in vitro systems for long term maintenance. [Doctoral Dissertation]. University of Plymouth; 1999. Available from: http://hdl.handle.net/10026.1/2526


University of Canberra

13. McGrath, John Francis. Immunomodulation in the context of developing a nontypeable Haemophilus influenzae vaccine.

Degree: 2007, University of Canberra

 One of the major challenges of vaccine development is the conservation of immunogenicity and protective efficacy through the stages of design, production, formulation and delivery. The critical… (more)

Subjects/Keywords: vaccine development; Nontypeable Haemophilus influenzae; NTHi; bacterial ghosts; immunisation

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APA (6th Edition):

McGrath, J. F. (2007). Immunomodulation in the context of developing a nontypeable Haemophilus influenzae vaccine. (Thesis). University of Canberra. Retrieved from http://erl.canberra.edu.au./public/adt-AUC20070726.152419

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):

McGrath, John Francis. “Immunomodulation in the context of developing a nontypeable Haemophilus influenzae vaccine.” 2007. Thesis, University of Canberra. Accessed June 25, 2019. http://erl.canberra.edu.au./public/adt-AUC20070726.152419.

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

MLA Handbook (7th Edition):

McGrath, John Francis. “Immunomodulation in the context of developing a nontypeable Haemophilus influenzae vaccine.” 2007. Web. 25 Jun 2019.

Vancouver:

McGrath JF. Immunomodulation in the context of developing a nontypeable Haemophilus influenzae vaccine. [Internet] [Thesis]. University of Canberra; 2007. [cited 2019 Jun 25]. Available from: http://erl.canberra.edu.au./public/adt-AUC20070726.152419.

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

Council of Science Editors:

McGrath JF. Immunomodulation in the context of developing a nontypeable Haemophilus influenzae vaccine. [Thesis]. University of Canberra; 2007. Available from: http://erl.canberra.edu.au./public/adt-AUC20070726.152419

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


Jawaharlal Nehru University

14. Srinivasan, J. Construction and development of a Vaccinia based recombinant Antifertility vaccine; -.

Degree: National Institute of Immunology, 2015, Jawaharlal Nehru University

None

Bibliography p.108-120

Advisors/Committee Members: Talwar,G P.

Subjects/Keywords: Antifertility vaccine; Construction; development; Vaccinia based recombinant

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APA (6th Edition):

Srinivasan, J. (2015). Construction and development of a Vaccinia based recombinant Antifertility vaccine; -. (Thesis). Jawaharlal Nehru University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/32487

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):

Srinivasan, J. “Construction and development of a Vaccinia based recombinant Antifertility vaccine; -.” 2015. Thesis, Jawaharlal Nehru University. Accessed June 25, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/32487.

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

MLA Handbook (7th Edition):

Srinivasan, J. “Construction and development of a Vaccinia based recombinant Antifertility vaccine; -.” 2015. Web. 25 Jun 2019.

Vancouver:

Srinivasan J. Construction and development of a Vaccinia based recombinant Antifertility vaccine; -. [Internet] [Thesis]. Jawaharlal Nehru University; 2015. [cited 2019 Jun 25]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/32487.

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

Council of Science Editors:

Srinivasan J. Construction and development of a Vaccinia based recombinant Antifertility vaccine; -. [Thesis]. Jawaharlal Nehru University; 2015. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/32487

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


University of Plymouth

15. Hurley, Louise Margaret. Ichthyophthirius multifiliis Fouquet : development and assessment of in vitro systems for long term maintenance.

Degree: PhD, 1999, University of Plymouth

 Twelve isolates of Ichthyophthirius multifiliis were successfully established and maintained by serial passage through naïve carp, for a maximum of 39 laboratory cycles. The management… (more)

Subjects/Keywords: 639.8; Fish cell culture; Vaccine development; Infection

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APA (6th Edition):

Hurley, L. M. (1999). Ichthyophthirius multifiliis Fouquet : development and assessment of in vitro systems for long term maintenance. (Doctoral Dissertation). University of Plymouth. Retrieved from http://hdl.handle.net/10026.1/785

Chicago Manual of Style (16th Edition):

Hurley, Louise Margaret. “Ichthyophthirius multifiliis Fouquet : development and assessment of in vitro systems for long term maintenance.” 1999. Doctoral Dissertation, University of Plymouth. Accessed June 25, 2019. http://hdl.handle.net/10026.1/785.

MLA Handbook (7th Edition):

Hurley, Louise Margaret. “Ichthyophthirius multifiliis Fouquet : development and assessment of in vitro systems for long term maintenance.” 1999. Web. 25 Jun 2019.

Vancouver:

Hurley LM. Ichthyophthirius multifiliis Fouquet : development and assessment of in vitro systems for long term maintenance. [Internet] [Doctoral dissertation]. University of Plymouth; 1999. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10026.1/785.

Council of Science Editors:

Hurley LM. Ichthyophthirius multifiliis Fouquet : development and assessment of in vitro systems for long term maintenance. [Doctoral Dissertation]. University of Plymouth; 1999. Available from: http://hdl.handle.net/10026.1/785


University of Toledo Health Science Campus

16. Tarcha, Eric J. Application of Immunoproteomics and Bioinformatics to coccidioidomycosis Vaccinology.

Degree: PhD, College of Graduate Studies, 2006, University of Toledo Health Science Campus

 Coccidioides is a primary fungal pathogen endemic to the alkaline desert soil of ||the Southwestern United States and the etiological agent of coccidioidomycosis (Valley fever),… (more)

Subjects/Keywords: vaccine development; multivalent vaccines; bioinformatics; proteomics; coccidioides

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

APA (6th Edition):

Tarcha, E. J. (2006). Application of Immunoproteomics and Bioinformatics to coccidioidomycosis Vaccinology. (Doctoral Dissertation). University of Toledo Health Science Campus. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=mco1154441973

Chicago Manual of Style (16th Edition):

Tarcha, Eric J. “Application of Immunoproteomics and Bioinformatics to coccidioidomycosis Vaccinology.” 2006. Doctoral Dissertation, University of Toledo Health Science Campus. Accessed June 25, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=mco1154441973.

MLA Handbook (7th Edition):

Tarcha, Eric J. “Application of Immunoproteomics and Bioinformatics to coccidioidomycosis Vaccinology.” 2006. Web. 25 Jun 2019.

Vancouver:

Tarcha EJ. Application of Immunoproteomics and Bioinformatics to coccidioidomycosis Vaccinology. [Internet] [Doctoral dissertation]. University of Toledo Health Science Campus; 2006. [cited 2019 Jun 25]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1154441973.

Council of Science Editors:

Tarcha EJ. Application of Immunoproteomics and Bioinformatics to coccidioidomycosis Vaccinology. [Doctoral Dissertation]. University of Toledo Health Science Campus; 2006. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1154441973


Queensland University of Technology

17. Carey, Alison Jane. Development of novel vaccine strategies to prevent genital tract chlamydial infections.

Degree: 2010, Queensland University of Technology

 Chlamydia trachomatis is the most prevalent bacterial sexually transmitted infection in the developed world and the leading cause of preventable blindness worldwide. As reported by… (more)

Subjects/Keywords: Chlamydia trachomatis; Chlamydia muridarum; female genital tract; ascending infection; inflammation; hydrosalpinx; vaccine development; timing of vaccination; persistent infection

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

APA (6th Edition):

Carey, A. J. (2010). Development of novel vaccine strategies to prevent genital tract chlamydial infections. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/48734/

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):

Carey, Alison Jane. “Development of novel vaccine strategies to prevent genital tract chlamydial infections.” 2010. Thesis, Queensland University of Technology. Accessed June 25, 2019. https://eprints.qut.edu.au/48734/.

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

MLA Handbook (7th Edition):

Carey, Alison Jane. “Development of novel vaccine strategies to prevent genital tract chlamydial infections.” 2010. Web. 25 Jun 2019.

Vancouver:

Carey AJ. Development of novel vaccine strategies to prevent genital tract chlamydial infections. [Internet] [Thesis]. Queensland University of Technology; 2010. [cited 2019 Jun 25]. Available from: https://eprints.qut.edu.au/48734/.

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

Council of Science Editors:

Carey AJ. Development of novel vaccine strategies to prevent genital tract chlamydial infections. [Thesis]. Queensland University of Technology; 2010. Available from: https://eprints.qut.edu.au/48734/

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

18. R. Capelli. COMPUTATIONAL MODELING OF PROTEINS: FROM STATISTICAL MECHANICS TO IMMUNOLOGY.

Degree: 2017, Università degli Studi di Milano

 One of the biggest revolutions occurred during the second half of the 20th century in physics was the introduction of computers in research. In particular,… (more)

Subjects/Keywords: Free energy calculations; Structural vaccinology; non-equilibrium simulations; Protein folding; Protein design; Vaccine development; Settore FIS/03 - Fisica della Materia

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

APA (6th Edition):

Capelli, R. (2017). COMPUTATIONAL MODELING OF PROTEINS: FROM STATISTICAL MECHANICS TO IMMUNOLOGY. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/527950

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):

Capelli, R.. “COMPUTATIONAL MODELING OF PROTEINS: FROM STATISTICAL MECHANICS TO IMMUNOLOGY.” 2017. Thesis, Università degli Studi di Milano. Accessed June 25, 2019. http://hdl.handle.net/2434/527950.

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

MLA Handbook (7th Edition):

Capelli, R.. “COMPUTATIONAL MODELING OF PROTEINS: FROM STATISTICAL MECHANICS TO IMMUNOLOGY.” 2017. Web. 25 Jun 2019.

Vancouver:

Capelli R. COMPUTATIONAL MODELING OF PROTEINS: FROM STATISTICAL MECHANICS TO IMMUNOLOGY. [Internet] [Thesis]. Università degli Studi di Milano; 2017. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/2434/527950.

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

Council of Science Editors:

Capelli R. COMPUTATIONAL MODELING OF PROTEINS: FROM STATISTICAL MECHANICS TO IMMUNOLOGY. [Thesis]. Università degli Studi di Milano; 2017. Available from: http://hdl.handle.net/2434/527950

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


University of Texas Medical Branch – Galveston

19. [No author]. Developing Methods to Study Pathogenesis and Immune Response to HSV-2 in the Guinea Pig Model .

Degree: University of Texas Medical Branch – Galveston

 In order to develop an effective vaccine for HSV-2 it is important to adequately understand the immune response in the proper animal model. Guinea pigs… (more)

Subjects/Keywords: Virology; Vaccine development; HSV-2; guinea pig

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

APA (6th Edition):

author], [. (n.d.). Developing Methods to Study Pathogenesis and Immune Response to HSV-2 in the Guinea Pig Model . (Thesis). University of Texas Medical Branch – Galveston. Retrieved from http://hdl.handle.net/2152.3/9430

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

Chicago Manual of Style (16th Edition):

author], [No. “Developing Methods to Study Pathogenesis and Immune Response to HSV-2 in the Guinea Pig Model .” Thesis, University of Texas Medical Branch – Galveston. Accessed June 25, 2019. http://hdl.handle.net/2152.3/9430.

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

MLA Handbook (7th Edition):

author], [No. “Developing Methods to Study Pathogenesis and Immune Response to HSV-2 in the Guinea Pig Model .” Web. 25 Jun 2019.

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

Vancouver:

author] [. Developing Methods to Study Pathogenesis and Immune Response to HSV-2 in the Guinea Pig Model . [Internet] [Thesis]. University of Texas Medical Branch – Galveston; [cited 2019 Jun 25]. Available from: http://hdl.handle.net/2152.3/9430.

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

Council of Science Editors:

author] [. Developing Methods to Study Pathogenesis and Immune Response to HSV-2 in the Guinea Pig Model . [Thesis]. University of Texas Medical Branch – Galveston; Available from: http://hdl.handle.net/2152.3/9430

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


University of Texas Medical Branch – Galveston

20. [No author]. Characterization of the Burkholderia mallei ∆tonB Mutant and its Potential as a Backbone Attenuated Strain for Vaccine Development .

Degree: University of Texas Medical Branch – Galveston

 In this study, a Burkholderia mallei ∆tonB mutant deficient in iron acquisition was constructed, characterized and evaluated for its protective properties in acute inhalational mouse… (more)

Subjects/Keywords: Burkholderia mallei; vaccine development; tonB; live attenuated mutant

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

APA (6th Edition):

author], [. (n.d.). Characterization of the Burkholderia mallei ∆tonB Mutant and its Potential as a Backbone Attenuated Strain for Vaccine Development . (Thesis). University of Texas Medical Branch – Galveston. Retrieved from http://hdl.handle.net/2152.3/723

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

Chicago Manual of Style (16th Edition):

author], [No. “Characterization of the Burkholderia mallei ∆tonB Mutant and its Potential as a Backbone Attenuated Strain for Vaccine Development .” Thesis, University of Texas Medical Branch – Galveston. Accessed June 25, 2019. http://hdl.handle.net/2152.3/723.

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

MLA Handbook (7th Edition):

author], [No. “Characterization of the Burkholderia mallei ∆tonB Mutant and its Potential as a Backbone Attenuated Strain for Vaccine Development .” Web. 25 Jun 2019.

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

Vancouver:

author] [. Characterization of the Burkholderia mallei ∆tonB Mutant and its Potential as a Backbone Attenuated Strain for Vaccine Development . [Internet] [Thesis]. University of Texas Medical Branch – Galveston; [cited 2019 Jun 25]. Available from: http://hdl.handle.net/2152.3/723.

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

Council of Science Editors:

author] [. Characterization of the Burkholderia mallei ∆tonB Mutant and its Potential as a Backbone Attenuated Strain for Vaccine Development . [Thesis]. University of Texas Medical Branch – Galveston; Available from: http://hdl.handle.net/2152.3/723

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


University of Texas Medical Branch – Galveston

21. [No author]. Yersinia pestis CO92 mutant deleted for the genes encoding Braun lipoprotein and plasminogen activator protease: Characterization of a potential live-attenuated vaccine candidate .

Degree: University of Texas Medical Branch – Galveston

 There is no FDA-approved vaccine against Yersinia pestis, the causative agent of bubonic and pneumonic plague. Since both humoral- and cell- mediated immunity are essential… (more)

Subjects/Keywords: Yersinia pestis; vaccine development; plasminogen activator protease; Braun lipoprotein

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

APA (6th Edition):

author], [. (n.d.). Yersinia pestis CO92 mutant deleted for the genes encoding Braun lipoprotein and plasminogen activator protease: Characterization of a potential live-attenuated vaccine candidate . (Thesis). University of Texas Medical Branch – Galveston. Retrieved from http://hdl.handle.net/2152.3/726

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

Chicago Manual of Style (16th Edition):

author], [No. “Yersinia pestis CO92 mutant deleted for the genes encoding Braun lipoprotein and plasminogen activator protease: Characterization of a potential live-attenuated vaccine candidate .” Thesis, University of Texas Medical Branch – Galveston. Accessed June 25, 2019. http://hdl.handle.net/2152.3/726.

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

MLA Handbook (7th Edition):

author], [No. “Yersinia pestis CO92 mutant deleted for the genes encoding Braun lipoprotein and plasminogen activator protease: Characterization of a potential live-attenuated vaccine candidate .” Web. 25 Jun 2019.

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

Vancouver:

author] [. Yersinia pestis CO92 mutant deleted for the genes encoding Braun lipoprotein and plasminogen activator protease: Characterization of a potential live-attenuated vaccine candidate . [Internet] [Thesis]. University of Texas Medical Branch – Galveston; [cited 2019 Jun 25]. Available from: http://hdl.handle.net/2152.3/726.

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

Council of Science Editors:

author] [. Yersinia pestis CO92 mutant deleted for the genes encoding Braun lipoprotein and plasminogen activator protease: Characterization of a potential live-attenuated vaccine candidate . [Thesis]. University of Texas Medical Branch – Galveston; Available from: http://hdl.handle.net/2152.3/726

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


University of Texas Medical Branch – Galveston

22. [No author]. Developing Methods to Study Pathogenesis and Immune Response to HSV-2 in the Guinea Pig Model .

Degree: University of Texas Medical Branch – Galveston

 In order to develop an effective vaccine for HSV-2 it is important to adequately understand the immune response in the proper animal model. Guinea pigs… (more)

Subjects/Keywords: Virology; Vaccine development; HSV-2; guinea pig

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

author], [. (n.d.). Developing Methods to Study Pathogenesis and Immune Response to HSV-2 in the Guinea Pig Model . (Thesis). University of Texas Medical Branch – Galveston. Retrieved from http://hdl.handle.net/2152.3/10718

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

Chicago Manual of Style (16th Edition):

author], [No. “Developing Methods to Study Pathogenesis and Immune Response to HSV-2 in the Guinea Pig Model .” Thesis, University of Texas Medical Branch – Galveston. Accessed June 25, 2019. http://hdl.handle.net/2152.3/10718.

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

MLA Handbook (7th Edition):

author], [No. “Developing Methods to Study Pathogenesis and Immune Response to HSV-2 in the Guinea Pig Model .” Web. 25 Jun 2019.

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

Vancouver:

author] [. Developing Methods to Study Pathogenesis and Immune Response to HSV-2 in the Guinea Pig Model . [Internet] [Thesis]. University of Texas Medical Branch – Galveston; [cited 2019 Jun 25]. Available from: http://hdl.handle.net/2152.3/10718.

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

Council of Science Editors:

author] [. Developing Methods to Study Pathogenesis and Immune Response to HSV-2 in the Guinea Pig Model . [Thesis]. University of Texas Medical Branch – Galveston; Available from: http://hdl.handle.net/2152.3/10718

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


University of Texas Medical Branch – Galveston

23. [No author]. Using the single-cycle flavivirus particle replivax to study flavivirus replication and immune response .

Degree: University of Texas Medical Branch – Galveston

 RepliVAX is a novel single-cycle flavivirus (SCFV) vaccine platform, which contains a deletion in the capsid (C) gene of West Nile virus (WNV) that prevents… (more)

Subjects/Keywords: Flavivirus; WNV; RepliVAX; viral immunology; vaccine development

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

APA (6th Edition):

author], [. (n.d.). Using the single-cycle flavivirus particle replivax to study flavivirus replication and immune response . (Thesis). University of Texas Medical Branch – Galveston. Retrieved from http://hdl.handle.net/2152.3/704

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

Chicago Manual of Style (16th Edition):

author], [No. “Using the single-cycle flavivirus particle replivax to study flavivirus replication and immune response .” Thesis, University of Texas Medical Branch – Galveston. Accessed June 25, 2019. http://hdl.handle.net/2152.3/704.

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

MLA Handbook (7th Edition):

author], [No. “Using the single-cycle flavivirus particle replivax to study flavivirus replication and immune response .” Web. 25 Jun 2019.

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

Vancouver:

author] [. Using the single-cycle flavivirus particle replivax to study flavivirus replication and immune response . [Internet] [Thesis]. University of Texas Medical Branch – Galveston; [cited 2019 Jun 25]. Available from: http://hdl.handle.net/2152.3/704.

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

Council of Science Editors:

author] [. Using the single-cycle flavivirus particle replivax to study flavivirus replication and immune response . [Thesis]. University of Texas Medical Branch – Galveston; Available from: http://hdl.handle.net/2152.3/704

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


Seton Hall University

24. Devenney, Kyle. Characterization of the Protective Role of Th17 Cells in an Fc Receptor-Targeted Vaccine Strategy Against Fracisella tularensis Infection.

Degree: MS Biology, Biology, 2018, Seton Hall University

  Using a murine model, we have previously showed that targeting an inactivated form of F.tularensis (iFt) bacteria to Fcg receptors by utilizing an IgG2a,… (more)

Subjects/Keywords: T helper; Th17; Fc receptor; FcR-targeting; Francisella tularensis; vaccine development; Bacteriology; Cell Biology; Immunology of Infectious Disease

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

APA (6th Edition):

Devenney, K. (2018). Characterization of the Protective Role of Th17 Cells in an Fc Receptor-Targeted Vaccine Strategy Against Fracisella tularensis Infection. (Doctoral Dissertation). Seton Hall University. Retrieved from https://scholarship.shu.edu/dissertations/2588

Chicago Manual of Style (16th Edition):

Devenney, Kyle. “Characterization of the Protective Role of Th17 Cells in an Fc Receptor-Targeted Vaccine Strategy Against Fracisella tularensis Infection.” 2018. Doctoral Dissertation, Seton Hall University. Accessed June 25, 2019. https://scholarship.shu.edu/dissertations/2588.

MLA Handbook (7th Edition):

Devenney, Kyle. “Characterization of the Protective Role of Th17 Cells in an Fc Receptor-Targeted Vaccine Strategy Against Fracisella tularensis Infection.” 2018. Web. 25 Jun 2019.

Vancouver:

Devenney K. Characterization of the Protective Role of Th17 Cells in an Fc Receptor-Targeted Vaccine Strategy Against Fracisella tularensis Infection. [Internet] [Doctoral dissertation]. Seton Hall University; 2018. [cited 2019 Jun 25]. Available from: https://scholarship.shu.edu/dissertations/2588.

Council of Science Editors:

Devenney K. Characterization of the Protective Role of Th17 Cells in an Fc Receptor-Targeted Vaccine Strategy Against Fracisella tularensis Infection. [Doctoral Dissertation]. Seton Hall University; 2018. Available from: https://scholarship.shu.edu/dissertations/2588


University of Pennsylvania

25. Weiss, Gretchen E. The Acquisition of Human B Cell Memory in Response to Plasmodium Falciparum Malaria.

Degree: 2010, University of Pennsylvania

 Immunity to Plasmodium falciparum (Pf), the most deadly agent of malaria, is only acquired after years of repeated infections and appears to wane rapidly without… (more)

Subjects/Keywords: B cell; malaria; pathogen-host interaction; immune modulation; vaccine development; Biology; Immunity; Immunology of Infectious Disease; Medical Immunology; Parasitology

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

APA (6th Edition):

Weiss, G. E. (2010). The Acquisition of Human B Cell Memory in Response to Plasmodium Falciparum Malaria. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/210

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):

Weiss, Gretchen E. “The Acquisition of Human B Cell Memory in Response to Plasmodium Falciparum Malaria.” 2010. Thesis, University of Pennsylvania. Accessed June 25, 2019. https://repository.upenn.edu/edissertations/210.

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

MLA Handbook (7th Edition):

Weiss, Gretchen E. “The Acquisition of Human B Cell Memory in Response to Plasmodium Falciparum Malaria.” 2010. Web. 25 Jun 2019.

Vancouver:

Weiss GE. The Acquisition of Human B Cell Memory in Response to Plasmodium Falciparum Malaria. [Internet] [Thesis]. University of Pennsylvania; 2010. [cited 2019 Jun 25]. Available from: https://repository.upenn.edu/edissertations/210.

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

Council of Science Editors:

Weiss GE. The Acquisition of Human B Cell Memory in Response to Plasmodium Falciparum Malaria. [Thesis]. University of Pennsylvania; 2010. Available from: https://repository.upenn.edu/edissertations/210

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


University of Pretoria

26. Espach, Anel. The Cloning and expression of the Rift Valley Fever G genes for the development of a DNA vaccine.

Degree: Microbiology and Plant Pathology, 2007, University of Pretoria

Please read the abstract in the 00front part of this document Advisors/Committee Members: Prof L H Nel (advisor).

Subjects/Keywords: Vaccine development; Rift valley fever genes genetic vectors; Rift valley fever virus diseases vaccine developm; UCTD

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

APA (6th Edition):

Espach, A. (2007). The Cloning and expression of the Rift Valley Fever G genes for the development of a DNA vaccine. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/23191

Chicago Manual of Style (16th Edition):

Espach, Anel. “The Cloning and expression of the Rift Valley Fever G genes for the development of a DNA vaccine.” 2007. Masters Thesis, University of Pretoria. Accessed June 25, 2019. http://hdl.handle.net/2263/23191.

MLA Handbook (7th Edition):

Espach, Anel. “The Cloning and expression of the Rift Valley Fever G genes for the development of a DNA vaccine.” 2007. Web. 25 Jun 2019.

Vancouver:

Espach A. The Cloning and expression of the Rift Valley Fever G genes for the development of a DNA vaccine. [Internet] [Masters thesis]. University of Pretoria; 2007. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/2263/23191.

Council of Science Editors:

Espach A. The Cloning and expression of the Rift Valley Fever G genes for the development of a DNA vaccine. [Masters Thesis]. University of Pretoria; 2007. Available from: http://hdl.handle.net/2263/23191


University of Pretoria

27. [No author]. The Cloning and expression of the Rift Valley Fever G genes for the development of a DNA vaccine .

Degree: 2007, University of Pretoria

Please read the abstract in the 00front part of this document Advisors/Committee Members: Prof L H Nel (advisor).

Subjects/Keywords: Vaccine development; Rift valley fever genes genetic vectors; Rift valley fever virus diseases vaccine developm; UCTD

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

APA (6th Edition):

author], [. (2007). The Cloning and expression of the Rift Valley Fever G genes for the development of a DNA vaccine . (Masters Thesis). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-03152007-111852/

Chicago Manual of Style (16th Edition):

author], [No. “The Cloning and expression of the Rift Valley Fever G genes for the development of a DNA vaccine .” 2007. Masters Thesis, University of Pretoria. Accessed June 25, 2019. http://upetd.up.ac.za/thesis/available/etd-03152007-111852/.

MLA Handbook (7th Edition):

author], [No. “The Cloning and expression of the Rift Valley Fever G genes for the development of a DNA vaccine .” 2007. Web. 25 Jun 2019.

Vancouver:

author] [. The Cloning and expression of the Rift Valley Fever G genes for the development of a DNA vaccine . [Internet] [Masters thesis]. University of Pretoria; 2007. [cited 2019 Jun 25]. Available from: http://upetd.up.ac.za/thesis/available/etd-03152007-111852/.

Council of Science Editors:

author] [. The Cloning and expression of the Rift Valley Fever G genes for the development of a DNA vaccine . [Masters Thesis]. University of Pretoria; 2007. Available from: http://upetd.up.ac.za/thesis/available/etd-03152007-111852/


University of Guelph

28. Wu, Anson. Identification of Flavobacterium psychrophilum Vaccine Candidates Using Comparative Genomics and Reverse Vaccinology .

Degree: 2015, University of Guelph

 The Gram-negative bacterium Flavobacterium psychrophilum is the etiological agent of Bacterial Cold Water Disease and Rainbow Trout Fry Syndrome in salmonid fishes, diseases that cause… (more)

Subjects/Keywords: Flavobacterium psychrophilum; Bacterial cold water disease; Rainbow trout fry syndrome; Fish pathogen; Bioinformatics; Comparative genomics; Reverse vaccinology; Gram negative; Psychrotolerant; Vaccine development

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

APA (6th Edition):

Wu, A. (2015). Identification of Flavobacterium psychrophilum Vaccine Candidates Using Comparative Genomics and Reverse Vaccinology . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9098

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):

Wu, Anson. “Identification of Flavobacterium psychrophilum Vaccine Candidates Using Comparative Genomics and Reverse Vaccinology .” 2015. Thesis, University of Guelph. Accessed June 25, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9098.

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

MLA Handbook (7th Edition):

Wu, Anson. “Identification of Flavobacterium psychrophilum Vaccine Candidates Using Comparative Genomics and Reverse Vaccinology .” 2015. Web. 25 Jun 2019.

Vancouver:

Wu A. Identification of Flavobacterium psychrophilum Vaccine Candidates Using Comparative Genomics and Reverse Vaccinology . [Internet] [Thesis]. University of Guelph; 2015. [cited 2019 Jun 25]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9098.

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

Council of Science Editors:

Wu A. Identification of Flavobacterium psychrophilum Vaccine Candidates Using Comparative Genomics and Reverse Vaccinology . [Thesis]. University of Guelph; 2015. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9098

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


University of Technology, Sydney

29. Raymond, BBA. Molecular interactions between Mycoplasma hyopneumoniae and host cells.

Degree: 2015, University of Technology, Sydney

 The Mycoplasmas are a group of wall-less bacteria belonging to the Mollicutes that are believed to have diverged from the Gram-positive Firmicutes. Mollicutes have undergone… (more)

Subjects/Keywords: Mycoplasma hyopneumoniae.; Molecular interactions.; Gram-positive Firmicutes.; Porcine enzootic pneumonia.; Epithelial barrier.; Dissemination to distal tissue sites.; Control of important veterinary disease.; Endoproteolytic processing.; Vaccine development programs.

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

APA (6th Edition):

Raymond, B. (2015). Molecular interactions between Mycoplasma hyopneumoniae and host cells. (Thesis). University of Technology, Sydney. Retrieved from http://hdl.handle.net/10453/39235

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):

Raymond, BBA. “Molecular interactions between Mycoplasma hyopneumoniae and host cells.” 2015. Thesis, University of Technology, Sydney. Accessed June 25, 2019. http://hdl.handle.net/10453/39235.

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

MLA Handbook (7th Edition):

Raymond, BBA. “Molecular interactions between Mycoplasma hyopneumoniae and host cells.” 2015. Web. 25 Jun 2019.

Vancouver:

Raymond B. Molecular interactions between Mycoplasma hyopneumoniae and host cells. [Internet] [Thesis]. University of Technology, Sydney; 2015. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10453/39235.

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

Council of Science Editors:

Raymond B. Molecular interactions between Mycoplasma hyopneumoniae and host cells. [Thesis]. University of Technology, Sydney; 2015. Available from: http://hdl.handle.net/10453/39235

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


Universiteit Utrecht

30. Geurtsen, J.J.G. Improving pertussis vaccines by lipopolysaccharide engineering.

Degree: 2007, Universiteit Utrecht

 Pertussis or whooping cough is a highly contagious respiratory tract disease that is caused by the Gram-negative bacterium Bordetella pertussis. Introduction of whole-cell pertussis (wP)… (more)

Subjects/Keywords: Biologie; Bordetella pertussis; bacterial outer membrane; vaccine development; whole-cell pertussis vaccines; acellular pertussis vaccines; lipopolysaccharide; whooping cough; endotoxin; adjuvant; serine hydrolases

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Geurtsen, J. J. G. (2007). Improving pertussis vaccines by lipopolysaccharide engineering. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/21598

Chicago Manual of Style (16th Edition):

Geurtsen, J J G. “Improving pertussis vaccines by lipopolysaccharide engineering.” 2007. Doctoral Dissertation, Universiteit Utrecht. Accessed June 25, 2019. http://dspace.library.uu.nl:8080/handle/1874/21598.

MLA Handbook (7th Edition):

Geurtsen, J J G. “Improving pertussis vaccines by lipopolysaccharide engineering.” 2007. Web. 25 Jun 2019.

Vancouver:

Geurtsen JJG. Improving pertussis vaccines by lipopolysaccharide engineering. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2007. [cited 2019 Jun 25]. Available from: http://dspace.library.uu.nl:8080/handle/1874/21598.

Council of Science Editors:

Geurtsen JJG. Improving pertussis vaccines by lipopolysaccharide engineering. [Doctoral Dissertation]. Universiteit Utrecht; 2007. Available from: http://dspace.library.uu.nl:8080/handle/1874/21598

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