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You searched for subject:(vaccine design). Showing records 1 – 30 of 35 total matches.

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1. Jaiswal Varun. Development of Immunoinformatics Tools for Vaccine Design;.

Degree: 2014, Jaypee University of Information Technology, Solan

Though vaccines against many diseases are available but those are not effective when strain variability is very high and immune response is poor These strain… (more)

Subjects/Keywords: Adhesin; Epitope-based Vaccine Candidate; Host Pathogen Interaction; Jenner; Universal Influenza Vaccine (UIV); Vaccine Design

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

APA (6th Edition):

Varun, J. (2014). Development of Immunoinformatics Tools for Vaccine Design;. (Thesis). Jaypee University of Information Technology, Solan. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/26246

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):

Varun, Jaiswal. “Development of Immunoinformatics Tools for Vaccine Design;.” 2014. Thesis, Jaypee University of Information Technology, Solan. Accessed January 19, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/26246.

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

MLA Handbook (7th Edition):

Varun, Jaiswal. “Development of Immunoinformatics Tools for Vaccine Design;.” 2014. Web. 19 Jan 2020.

Vancouver:

Varun J. Development of Immunoinformatics Tools for Vaccine Design;. [Internet] [Thesis]. Jaypee University of Information Technology, Solan; 2014. [cited 2020 Jan 19]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/26246.

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

Council of Science Editors:

Varun J. Development of Immunoinformatics Tools for Vaccine Design;. [Thesis]. Jaypee University of Information Technology, Solan; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/26246

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


University of Rochester

2. Weaver, Jason Michael. The Immunodominance of CD4 T Cell Epitopes is Peptide Intrinsic: Implications for Rational Vaccine Design.

Degree: PhD, 2010, University of Rochester

 Establishment of an immune response that is focused on a limited number of peptide determinants expressed by a complex antigen or pathogen is a phenomenon… (more)

Subjects/Keywords: MHC; Peptide; T Cell Activation; Vaccine Design

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APA (6th Edition):

Weaver, J. M. (2010). The Immunodominance of CD4 T Cell Epitopes is Peptide Intrinsic: Implications for Rational Vaccine Design. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/9722

Chicago Manual of Style (16th Edition):

Weaver, Jason Michael. “The Immunodominance of CD4 T Cell Epitopes is Peptide Intrinsic: Implications for Rational Vaccine Design.” 2010. Doctoral Dissertation, University of Rochester. Accessed January 19, 2020. http://hdl.handle.net/1802/9722.

MLA Handbook (7th Edition):

Weaver, Jason Michael. “The Immunodominance of CD4 T Cell Epitopes is Peptide Intrinsic: Implications for Rational Vaccine Design.” 2010. Web. 19 Jan 2020.

Vancouver:

Weaver JM. The Immunodominance of CD4 T Cell Epitopes is Peptide Intrinsic: Implications for Rational Vaccine Design. [Internet] [Doctoral dissertation]. University of Rochester; 2010. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/1802/9722.

Council of Science Editors:

Weaver JM. The Immunodominance of CD4 T Cell Epitopes is Peptide Intrinsic: Implications for Rational Vaccine Design. [Doctoral Dissertation]. University of Rochester; 2010. Available from: http://hdl.handle.net/1802/9722


University of Cincinnati

3. Donauer, Stephanie. Determining the Post-Licensure Effectiveness of Pentavalent Rotavirus Vaccine using Observational Study Designs.

Degree: PhD, Medicine: Epidemiology (Environmental Health), 2013, University of Cincinnati

 The primary objective of this study is to determine the vaccine effectiveness (VE) of the pentavalent rotavirus vaccine (RV5) for preventing rotavirus-related hospitalizations and emergency… (more)

Subjects/Keywords: Epidemiology; rotavirus; vaccine effectiveness; study design

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APA (6th Edition):

Donauer, S. (2013). Determining the Post-Licensure Effectiveness of Pentavalent Rotavirus Vaccine using Observational Study Designs. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1368026785

Chicago Manual of Style (16th Edition):

Donauer, Stephanie. “Determining the Post-Licensure Effectiveness of Pentavalent Rotavirus Vaccine using Observational Study Designs.” 2013. Doctoral Dissertation, University of Cincinnati. Accessed January 19, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1368026785.

MLA Handbook (7th Edition):

Donauer, Stephanie. “Determining the Post-Licensure Effectiveness of Pentavalent Rotavirus Vaccine using Observational Study Designs.” 2013. Web. 19 Jan 2020.

Vancouver:

Donauer S. Determining the Post-Licensure Effectiveness of Pentavalent Rotavirus Vaccine using Observational Study Designs. [Internet] [Doctoral dissertation]. University of Cincinnati; 2013. [cited 2020 Jan 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1368026785.

Council of Science Editors:

Donauer S. Determining the Post-Licensure Effectiveness of Pentavalent Rotavirus Vaccine using Observational Study Designs. [Doctoral Dissertation]. University of Cincinnati; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1368026785

4. Odunsi, Adekunle Omatayo. Immunogenetic analysis of HLA Class II in premalignant disease of the cervix and correlation with HPV status.

Degree: PhD, 1999, Open University

 The human papilloma virus (HPY) infection has a causal association with cervical intraepithelial neoplasia (CIN) and cervical cancer. However, pre-malignant or malignant transformation is not… (more)

Subjects/Keywords: 572.8; HPV vaccine design

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APA (6th Edition):

Odunsi, A. O. (1999). Immunogenetic analysis of HLA Class II in premalignant disease of the cervix and correlation with HPV status. (Doctoral Dissertation). Open University. Retrieved from http://oro.open.ac.uk/54556/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.266420

Chicago Manual of Style (16th Edition):

Odunsi, Adekunle Omatayo. “Immunogenetic analysis of HLA Class II in premalignant disease of the cervix and correlation with HPV status.” 1999. Doctoral Dissertation, Open University. Accessed January 19, 2020. http://oro.open.ac.uk/54556/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.266420.

MLA Handbook (7th Edition):

Odunsi, Adekunle Omatayo. “Immunogenetic analysis of HLA Class II in premalignant disease of the cervix and correlation with HPV status.” 1999. Web. 19 Jan 2020.

Vancouver:

Odunsi AO. Immunogenetic analysis of HLA Class II in premalignant disease of the cervix and correlation with HPV status. [Internet] [Doctoral dissertation]. Open University; 1999. [cited 2020 Jan 19]. Available from: http://oro.open.ac.uk/54556/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.266420.

Council of Science Editors:

Odunsi AO. Immunogenetic analysis of HLA Class II in premalignant disease of the cervix and correlation with HPV status. [Doctoral Dissertation]. Open University; 1999. Available from: http://oro.open.ac.uk/54556/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.266420

5. Gupta, Hema Malini. GnRH structure and interactions : implications to vaccine design; -.

Degree: Immunology, 2014, Jawaharlal Nehru University

None

Reference P.145-160

Advisors/Committee Members: Salunke, D M.

Subjects/Keywords: Design; Interactions; Structur; Vaccine

Page 1

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APA (6th Edition):

Gupta, H. M. (2014). GnRH structure and interactions : implications to vaccine design; -. (Thesis). Jawaharlal Nehru University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/21238

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):

Gupta, Hema Malini. “GnRH structure and interactions : implications to vaccine design; -.” 2014. Thesis, Jawaharlal Nehru University. Accessed January 19, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/21238.

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

MLA Handbook (7th Edition):

Gupta, Hema Malini. “GnRH structure and interactions : implications to vaccine design; -.” 2014. Web. 19 Jan 2020.

Vancouver:

Gupta HM. GnRH structure and interactions : implications to vaccine design; -. [Internet] [Thesis]. Jawaharlal Nehru University; 2014. [cited 2020 Jan 19]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/21238.

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

Council of Science Editors:

Gupta HM. GnRH structure and interactions : implications to vaccine design; -. [Thesis]. Jawaharlal Nehru University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/21238

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


Brno University of Technology

6. Fux, Jan. Konstrukce dávkovače vakcíny .

Degree: 2014, Brno University of Technology

 Cílem této práce je provést konstrukční návrh zařízení pro dávkování vakcín proti vzteklině dané velikosti a tvaru. Vakcíny budou shazovány z letadla, tudíž je pro… (more)

Subjects/Keywords: Dávkovač; konstrukce; vakcína; vzteklina; Dispenser; design; vaccine; rabies

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APA (6th Edition):

Fux, J. (2014). Konstrukce dávkovače vakcíny . (Thesis). Brno University of Technology. Retrieved from http://hdl.handle.net/11012/32468

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):

Fux, Jan. “Konstrukce dávkovače vakcíny .” 2014. Thesis, Brno University of Technology. Accessed January 19, 2020. http://hdl.handle.net/11012/32468.

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

MLA Handbook (7th Edition):

Fux, Jan. “Konstrukce dávkovače vakcíny .” 2014. Web. 19 Jan 2020.

Vancouver:

Fux J. Konstrukce dávkovače vakcíny . [Internet] [Thesis]. Brno University of Technology; 2014. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/11012/32468.

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

Council of Science Editors:

Fux J. Konstrukce dávkovače vakcíny . [Thesis]. Brno University of Technology; 2014. Available from: http://hdl.handle.net/11012/32468

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

7. Zhang, Qiuye. Development of a Novel Vaccine Adjuvant System Utilizing an In Situ Implant System to Modified Release.

Degree: PhD, Pharmaceutical Sciences, 2014, University of Tennessee Health Science Center

  Pulsatile release formulations for single dose vaccines have been studied for many years because of the advantages that they may provide to vaccine administration… (more)

Subjects/Keywords: In Situ Implant; PLGA; Single dose vaccine; Vaccine adjuvant; Medicine and Health Sciences; Pharmaceutics and Drug Design; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Zhang, Q. (2014). Development of a Novel Vaccine Adjuvant System Utilizing an In Situ Implant System to Modified Release. (Doctoral Dissertation). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/321

Chicago Manual of Style (16th Edition):

Zhang, Qiuye. “Development of a Novel Vaccine Adjuvant System Utilizing an In Situ Implant System to Modified Release.” 2014. Doctoral Dissertation, University of Tennessee Health Science Center. Accessed January 19, 2020. https://dc.uthsc.edu/dissertations/321.

MLA Handbook (7th Edition):

Zhang, Qiuye. “Development of a Novel Vaccine Adjuvant System Utilizing an In Situ Implant System to Modified Release.” 2014. Web. 19 Jan 2020.

Vancouver:

Zhang Q. Development of a Novel Vaccine Adjuvant System Utilizing an In Situ Implant System to Modified Release. [Internet] [Doctoral dissertation]. University of Tennessee Health Science Center; 2014. [cited 2020 Jan 19]. Available from: https://dc.uthsc.edu/dissertations/321.

Council of Science Editors:

Zhang Q. Development of a Novel Vaccine Adjuvant System Utilizing an In Situ Implant System to Modified Release. [Doctoral Dissertation]. University of Tennessee Health Science Center; 2014. Available from: https://dc.uthsc.edu/dissertations/321


Duquesne University

8. Henkel, Matthew A. Evaluation of PilO Substrate Specificity Using Normally Non-Glycosylated Proteins in Pseudomonas Aeruginosa.

Degree: MS, Biological Sciences, 2009, Duquesne University

 P. aeruginosa 1244 (PA1244) possesses an O-linked glycosylation system by which the glycosyltransferase, PilO, transfers a single preassembled O-antigen repeating unit to the C-terminal serine… (more)

Subjects/Keywords: substrate specificity; PilO; peptide extension; Pseudomonas aeruginosa; O-linked glycosylation; vaccine design

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APA (6th Edition):

Henkel, M. A. (2009). Evaluation of PilO Substrate Specificity Using Normally Non-Glycosylated Proteins in Pseudomonas Aeruginosa. (Masters Thesis). Duquesne University. Retrieved from https://dsc.duq.edu/etd/646

Chicago Manual of Style (16th Edition):

Henkel, Matthew A. “Evaluation of PilO Substrate Specificity Using Normally Non-Glycosylated Proteins in Pseudomonas Aeruginosa.” 2009. Masters Thesis, Duquesne University. Accessed January 19, 2020. https://dsc.duq.edu/etd/646.

MLA Handbook (7th Edition):

Henkel, Matthew A. “Evaluation of PilO Substrate Specificity Using Normally Non-Glycosylated Proteins in Pseudomonas Aeruginosa.” 2009. Web. 19 Jan 2020.

Vancouver:

Henkel MA. Evaluation of PilO Substrate Specificity Using Normally Non-Glycosylated Proteins in Pseudomonas Aeruginosa. [Internet] [Masters thesis]. Duquesne University; 2009. [cited 2020 Jan 19]. Available from: https://dsc.duq.edu/etd/646.

Council of Science Editors:

Henkel MA. Evaluation of PilO Substrate Specificity Using Normally Non-Glycosylated Proteins in Pseudomonas Aeruginosa. [Masters Thesis]. Duquesne University; 2009. Available from: https://dsc.duq.edu/etd/646


University of California – Santa Cruz

9. Morales, Javier. V1/V2 domain scaffolds to improve the magnitude and quality of protective antibody responses to HIV-1.

Degree: Chemistry, 2014, University of California – Santa Cruz

 Two lines of investigation have highlighted the importance of antibodies to the V1/V2 domain of gp120 in providing protection from HIV-1 infection. First, the recent… (more)

Subjects/Keywords: Biochemistry; Biomedical engineering; Antibody; Glycosylation; HIV; Scaffolds; Structure based vaccine design; V1/V2

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APA (6th Edition):

Morales, J. (2014). V1/V2 domain scaffolds to improve the magnitude and quality of protective antibody responses to HIV-1. (Thesis). University of California – Santa Cruz. Retrieved from http://www.escholarship.org/uc/item/8164m878

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

Chicago Manual of Style (16th Edition):

Morales, Javier. “V1/V2 domain scaffolds to improve the magnitude and quality of protective antibody responses to HIV-1.” 2014. Thesis, University of California – Santa Cruz. Accessed January 19, 2020. http://www.escholarship.org/uc/item/8164m878.

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

MLA Handbook (7th Edition):

Morales, Javier. “V1/V2 domain scaffolds to improve the magnitude and quality of protective antibody responses to HIV-1.” 2014. Web. 19 Jan 2020.

Vancouver:

Morales J. V1/V2 domain scaffolds to improve the magnitude and quality of protective antibody responses to HIV-1. [Internet] [Thesis]. University of California – Santa Cruz; 2014. [cited 2020 Jan 19]. Available from: http://www.escholarship.org/uc/item/8164m878.

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

Council of Science Editors:

Morales J. V1/V2 domain scaffolds to improve the magnitude and quality of protective antibody responses to HIV-1. [Thesis]. University of California – Santa Cruz; 2014. Available from: http://www.escholarship.org/uc/item/8164m878

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


University of Melbourne

10. Gause, Katelyn T. Physicochemical and immunological assessment of mesoporous silica-templated particles for vaccine delivery applications.

Degree: 2015, University of Melbourne

 Routine vaccination was initiated in the early 20th century and is now considered one of the most beneficial health initiatives of all time. Despite their… (more)

Subjects/Keywords: vaccine; immunology; nanotechnology; particles; subunit antigen; rational design; protein antigen; mesoporous silica

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APA (6th Edition):

Gause, K. T. (2015). Physicochemical and immunological assessment of mesoporous silica-templated particles for vaccine delivery applications. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/58166

Chicago Manual of Style (16th Edition):

Gause, Katelyn T. “Physicochemical and immunological assessment of mesoporous silica-templated particles for vaccine delivery applications.” 2015. Doctoral Dissertation, University of Melbourne. Accessed January 19, 2020. http://hdl.handle.net/11343/58166.

MLA Handbook (7th Edition):

Gause, Katelyn T. “Physicochemical and immunological assessment of mesoporous silica-templated particles for vaccine delivery applications.” 2015. Web. 19 Jan 2020.

Vancouver:

Gause KT. Physicochemical and immunological assessment of mesoporous silica-templated particles for vaccine delivery applications. [Internet] [Doctoral dissertation]. University of Melbourne; 2015. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/11343/58166.

Council of Science Editors:

Gause KT. Physicochemical and immunological assessment of mesoporous silica-templated particles for vaccine delivery applications. [Doctoral Dissertation]. University of Melbourne; 2015. Available from: http://hdl.handle.net/11343/58166


University of Oxford

11. Behrens, Anna-Janina. Fine structure of the HIV-1 glycan shield.

Degree: PhD, 2017, University of Oxford

 The HIV-1 envelope glycoprotein trimer (Env) is covered by an extensive array of glycans that shield it from immune surveillance. The high density of glycans… (more)

Subjects/Keywords: 572; HIV-1 glycosylation analysis; mass spectrometry; HIV; N-glycosylation; Vaccine design; glycobiology

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APA (6th Edition):

Behrens, A. (2017). Fine structure of the HIV-1 glycan shield. (Doctoral Dissertation). University of Oxford. Retrieved from https://ora.ox.ac.uk/objects/uuid:3cec0ef7-c305-411e-a76b-125d5e7e9954 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.729117

Chicago Manual of Style (16th Edition):

Behrens, Anna-Janina. “Fine structure of the HIV-1 glycan shield.” 2017. Doctoral Dissertation, University of Oxford. Accessed January 19, 2020. https://ora.ox.ac.uk/objects/uuid:3cec0ef7-c305-411e-a76b-125d5e7e9954 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.729117.

MLA Handbook (7th Edition):

Behrens, Anna-Janina. “Fine structure of the HIV-1 glycan shield.” 2017. Web. 19 Jan 2020.

Vancouver:

Behrens A. Fine structure of the HIV-1 glycan shield. [Internet] [Doctoral dissertation]. University of Oxford; 2017. [cited 2020 Jan 19]. Available from: https://ora.ox.ac.uk/objects/uuid:3cec0ef7-c305-411e-a76b-125d5e7e9954 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.729117.

Council of Science Editors:

Behrens A. Fine structure of the HIV-1 glycan shield. [Doctoral Dissertation]. University of Oxford; 2017. Available from: https://ora.ox.ac.uk/objects/uuid:3cec0ef7-c305-411e-a76b-125d5e7e9954 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.729117


Georgia Tech

12. Crooke, Stephen Nicholas. Chemical and genetic modification of virus-like particles for applications in vaccine design and drug delivery.

Degree: PhD, Chemistry and Biochemistry, 2018, Georgia Tech

 Virus-like particles (VLPs) are multi-subunit protein assemblies that self-assemble into homogenous particles with periodic structure, making them ideal candidates for applications in biomedicine. This dissertation… (more)

Subjects/Keywords: Virus-like particles; Drug delivery; Vaccine design; Prodrug therapy; Protein-polymer materials

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APA (6th Edition):

Crooke, S. N. (2018). Chemical and genetic modification of virus-like particles for applications in vaccine design and drug delivery. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60247

Chicago Manual of Style (16th Edition):

Crooke, Stephen Nicholas. “Chemical and genetic modification of virus-like particles for applications in vaccine design and drug delivery.” 2018. Doctoral Dissertation, Georgia Tech. Accessed January 19, 2020. http://hdl.handle.net/1853/60247.

MLA Handbook (7th Edition):

Crooke, Stephen Nicholas. “Chemical and genetic modification of virus-like particles for applications in vaccine design and drug delivery.” 2018. Web. 19 Jan 2020.

Vancouver:

Crooke SN. Chemical and genetic modification of virus-like particles for applications in vaccine design and drug delivery. [Internet] [Doctoral dissertation]. Georgia Tech; 2018. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/1853/60247.

Council of Science Editors:

Crooke SN. Chemical and genetic modification of virus-like particles for applications in vaccine design and drug delivery. [Doctoral Dissertation]. Georgia Tech; 2018. Available from: http://hdl.handle.net/1853/60247


University of Washington

13. Ueda, George Thomas. Computational Design of Symmetric Protein Complexes with Implications for Vaccine and Biotherapeutic Development.

Degree: PhD, 2019, University of Washington

 Using a newly developed computational docking and scoring method combined with Rosetta two-sided interface design, we demonstrated accurate design of self-assembling oligomeric proteins that exhibit… (more)

Subjects/Keywords: Biotherapeutic; Computational; Design; Engineering; Protein; Vaccine; Biochemistry; Bioengineering; Computational chemistry; Biological chemistry

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APA (6th Edition):

Ueda, G. T. (2019). Computational Design of Symmetric Protein Complexes with Implications for Vaccine and Biotherapeutic Development. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/43303

Chicago Manual of Style (16th Edition):

Ueda, George Thomas. “Computational Design of Symmetric Protein Complexes with Implications for Vaccine and Biotherapeutic Development.” 2019. Doctoral Dissertation, University of Washington. Accessed January 19, 2020. http://hdl.handle.net/1773/43303.

MLA Handbook (7th Edition):

Ueda, George Thomas. “Computational Design of Symmetric Protein Complexes with Implications for Vaccine and Biotherapeutic Development.” 2019. Web. 19 Jan 2020.

Vancouver:

Ueda GT. Computational Design of Symmetric Protein Complexes with Implications for Vaccine and Biotherapeutic Development. [Internet] [Doctoral dissertation]. University of Washington; 2019. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/1773/43303.

Council of Science Editors:

Ueda GT. Computational Design of Symmetric Protein Complexes with Implications for Vaccine and Biotherapeutic Development. [Doctoral Dissertation]. University of Washington; 2019. Available from: http://hdl.handle.net/1773/43303


University of Oxford

14. von Delft, Annette Reingart. Implications of HCV genotype 3 specific immunity on cross-reactive vaccine design.

Degree: PhD, 2014, University of Oxford

 Hepatitis C virus (HCV) is a major global pathogen that infects an estimated 170 million people worldwide, and for which currently no vaccine is available.… (more)

Subjects/Keywords: 616.3; Medical sciences; Gastroenterology; Immunology; Viruses; Infectious diseases; Hepatitis C Virus; T-cell; genotype 3; cross-reactivity; Vaccine design

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APA (6th Edition):

von Delft, A. R. (2014). Implications of HCV genotype 3 specific immunity on cross-reactive vaccine design. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:f7daefac-3f4d-4040-ac6f-52c476d527be ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658472

Chicago Manual of Style (16th Edition):

von Delft, Annette Reingart. “Implications of HCV genotype 3 specific immunity on cross-reactive vaccine design.” 2014. Doctoral Dissertation, University of Oxford. Accessed January 19, 2020. http://ora.ox.ac.uk/objects/uuid:f7daefac-3f4d-4040-ac6f-52c476d527be ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658472.

MLA Handbook (7th Edition):

von Delft, Annette Reingart. “Implications of HCV genotype 3 specific immunity on cross-reactive vaccine design.” 2014. Web. 19 Jan 2020.

Vancouver:

von Delft AR. Implications of HCV genotype 3 specific immunity on cross-reactive vaccine design. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2020 Jan 19]. Available from: http://ora.ox.ac.uk/objects/uuid:f7daefac-3f4d-4040-ac6f-52c476d527be ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658472.

Council of Science Editors:

von Delft AR. Implications of HCV genotype 3 specific immunity on cross-reactive vaccine design. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:f7daefac-3f4d-4040-ac6f-52c476d527be ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658472

15. 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 January 19, 2020. 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. 19 Jan 2020.

Vancouver:

Capelli R. COMPUTATIONAL MODELING OF PROTEINS: FROM STATISTICAL MECHANICS TO IMMUNOLOGY. [Internet] [Thesis]. Università degli Studi di Milano; 2017. [cited 2020 Jan 19]. 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

16. HU YONGLI. IMMUNOINFORMATICS ANALYSIS OF HIV-1 PROTEOMIC DIVERSITY: IMPLICATIONS FOR VACCINE DESIGN.

Degree: 2014, National University of Singapore

Subjects/Keywords: Immunoinformatics; HIV-1; Proteins; viral diversity; vaccine design

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

APA (6th Edition):

YONGLI, H. (2014). IMMUNOINFORMATICS ANALYSIS OF HIV-1 PROTEOMIC DIVERSITY: IMPLICATIONS FOR VACCINE DESIGN. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/53781

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):

YONGLI, HU. “IMMUNOINFORMATICS ANALYSIS OF HIV-1 PROTEOMIC DIVERSITY: IMPLICATIONS FOR VACCINE DESIGN.” 2014. Thesis, National University of Singapore. Accessed January 19, 2020. http://scholarbank.nus.edu.sg/handle/10635/53781.

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

MLA Handbook (7th Edition):

YONGLI, HU. “IMMUNOINFORMATICS ANALYSIS OF HIV-1 PROTEOMIC DIVERSITY: IMPLICATIONS FOR VACCINE DESIGN.” 2014. Web. 19 Jan 2020.

Vancouver:

YONGLI H. IMMUNOINFORMATICS ANALYSIS OF HIV-1 PROTEOMIC DIVERSITY: IMPLICATIONS FOR VACCINE DESIGN. [Internet] [Thesis]. National University of Singapore; 2014. [cited 2020 Jan 19]. Available from: http://scholarbank.nus.edu.sg/handle/10635/53781.

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

Council of Science Editors:

YONGLI H. IMMUNOINFORMATICS ANALYSIS OF HIV-1 PROTEOMIC DIVERSITY: IMPLICATIONS FOR VACCINE DESIGN. [Thesis]. National University of Singapore; 2014. Available from: http://scholarbank.nus.edu.sg/handle/10635/53781

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


Iowa State University

17. Wagner, Danielle Ann. Design and evaluation of single-dose polyanhydride nanovaccines against bacterial respiratory pathogens.

Degree: 2019, Iowa State University

Design of a high-quality vaccine requires more than just initiation of a robust immune response, as there are several other factors that should be considered… (more)

Subjects/Keywords: immmunology; nanovaccine; respiratory pathogens; shelf stability; single dose; vaccine design; Allergy and Immunology; Immunology and Infectious Disease; Medical Immunology

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

APA (6th Edition):

Wagner, D. A. (2019). Design and evaluation of single-dose polyanhydride nanovaccines against bacterial respiratory pathogens. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/17116

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):

Wagner, Danielle Ann. “Design and evaluation of single-dose polyanhydride nanovaccines against bacterial respiratory pathogens.” 2019. Thesis, Iowa State University. Accessed January 19, 2020. https://lib.dr.iastate.edu/etd/17116.

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

MLA Handbook (7th Edition):

Wagner, Danielle Ann. “Design and evaluation of single-dose polyanhydride nanovaccines against bacterial respiratory pathogens.” 2019. Web. 19 Jan 2020.

Vancouver:

Wagner DA. Design and evaluation of single-dose polyanhydride nanovaccines against bacterial respiratory pathogens. [Internet] [Thesis]. Iowa State University; 2019. [cited 2020 Jan 19]. Available from: https://lib.dr.iastate.edu/etd/17116.

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

Council of Science Editors:

Wagner DA. Design and evaluation of single-dose polyanhydride nanovaccines against bacterial respiratory pathogens. [Thesis]. Iowa State University; 2019. Available from: https://lib.dr.iastate.edu/etd/17116

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


Iowa State University

18. Zimmerli, Mandy Kay. Identification and characterization of the major outer membrane proteins of Haemophilus parasuis for the rational development of a vaccine candidate and diagnostic for Glässer's disease.

Degree: 2011, Iowa State University

 Haemophilus parasuis is the causative agent of Glässer's disease, a respiratory illness in swine, which causes significant economic loss in the industry. To date, there… (more)

Subjects/Keywords: Biochemistry; Haemophilus parasuis; outer membrane protein P2; outer membrane protein P5; proteomics; reverse vaccinology; vaccine design; Biochemistry

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APA (6th Edition):

Zimmerli, M. K. (2011). Identification and characterization of the major outer membrane proteins of Haemophilus parasuis for the rational development of a vaccine candidate and diagnostic for Glässer's disease. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/14127

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):

Zimmerli, Mandy Kay. “Identification and characterization of the major outer membrane proteins of Haemophilus parasuis for the rational development of a vaccine candidate and diagnostic for Glässer's disease.” 2011. Thesis, Iowa State University. Accessed January 19, 2020. https://lib.dr.iastate.edu/etd/14127.

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

MLA Handbook (7th Edition):

Zimmerli, Mandy Kay. “Identification and characterization of the major outer membrane proteins of Haemophilus parasuis for the rational development of a vaccine candidate and diagnostic for Glässer's disease.” 2011. Web. 19 Jan 2020.

Vancouver:

Zimmerli MK. Identification and characterization of the major outer membrane proteins of Haemophilus parasuis for the rational development of a vaccine candidate and diagnostic for Glässer's disease. [Internet] [Thesis]. Iowa State University; 2011. [cited 2020 Jan 19]. Available from: https://lib.dr.iastate.edu/etd/14127.

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

Council of Science Editors:

Zimmerli MK. Identification and characterization of the major outer membrane proteins of Haemophilus parasuis for the rational development of a vaccine candidate and diagnostic for Glässer's disease. [Thesis]. Iowa State University; 2011. Available from: https://lib.dr.iastate.edu/etd/14127

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


University of Washington

19. Gewe, Mesfin Mulugeta. Spectrum of Somatic Hypermutations and Implication on Antibody Function: Case of the anti HIV-1 antibody, b12.

Degree: PhD, 2015, University of Washington

 Sequence diversity, ability to evade immune detection and establishment of human immunodeficiency virus type 1 (HIV-1) latent reservoirs present a formidable challenge to the development… (more)

Subjects/Keywords: Antibody Maturation; Biophysics; HIV; Structual Biology; Vaccine Design; Virology; Molecular biology; Immunology; Biochemistry; molecular and cellular biology

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

APA (6th Edition):

Gewe, M. M. (2015). Spectrum of Somatic Hypermutations and Implication on Antibody Function: Case of the anti HIV-1 antibody, b12. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/34062

Chicago Manual of Style (16th Edition):

Gewe, Mesfin Mulugeta. “Spectrum of Somatic Hypermutations and Implication on Antibody Function: Case of the anti HIV-1 antibody, b12.” 2015. Doctoral Dissertation, University of Washington. Accessed January 19, 2020. http://hdl.handle.net/1773/34062.

MLA Handbook (7th Edition):

Gewe, Mesfin Mulugeta. “Spectrum of Somatic Hypermutations and Implication on Antibody Function: Case of the anti HIV-1 antibody, b12.” 2015. Web. 19 Jan 2020.

Vancouver:

Gewe MM. Spectrum of Somatic Hypermutations and Implication on Antibody Function: Case of the anti HIV-1 antibody, b12. [Internet] [Doctoral dissertation]. University of Washington; 2015. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/1773/34062.

Council of Science Editors:

Gewe MM. Spectrum of Somatic Hypermutations and Implication on Antibody Function: Case of the anti HIV-1 antibody, b12. [Doctoral Dissertation]. University of Washington; 2015. Available from: http://hdl.handle.net/1773/34062


University of California – San Francisco

20. Stone, Jeffrey K. Understanding Viral Quasispecies, Viral Escape, and the Implications for the Design of Antiviral Strategies.

Degree: Biomedical Sciences, 2007, University of California – San Francisco

 RNA viruses, for many reasons, have evolved to be highly mutable, and as such readily escape antiviral drugs and other compounds designed to limit viral… (more)

Subjects/Keywords: Biology, Virology; Viral Quasispecies; Antiviral Design; Viral Escape; Vaccine Design

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

APA (6th Edition):

Stone, J. K. (2007). Understanding Viral Quasispecies, Viral Escape, and the Implications for the Design of Antiviral Strategies. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/5cc4t216

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):

Stone, Jeffrey K. “Understanding Viral Quasispecies, Viral Escape, and the Implications for the Design of Antiviral Strategies.” 2007. Thesis, University of California – San Francisco. Accessed January 19, 2020. http://www.escholarship.org/uc/item/5cc4t216.

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

MLA Handbook (7th Edition):

Stone, Jeffrey K. “Understanding Viral Quasispecies, Viral Escape, and the Implications for the Design of Antiviral Strategies.” 2007. Web. 19 Jan 2020.

Vancouver:

Stone JK. Understanding Viral Quasispecies, Viral Escape, and the Implications for the Design of Antiviral Strategies. [Internet] [Thesis]. University of California – San Francisco; 2007. [cited 2020 Jan 19]. Available from: http://www.escholarship.org/uc/item/5cc4t216.

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

Council of Science Editors:

Stone JK. Understanding Viral Quasispecies, Viral Escape, and the Implications for the Design of Antiviral Strategies. [Thesis]. University of California – San Francisco; 2007. Available from: http://www.escholarship.org/uc/item/5cc4t216

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


Indian Institute of Science

21. Chakraborty, Kausik. gp120 Immunogen Design And Characterization.

Degree: 2005, Indian Institute of Science

 HIV-1 is the causative agent for AIDS and has been a major focus of research for the past two decades. Though there is a combination… (more)

Subjects/Keywords: Human Immunodeficiency Virus (HIV); Immunogenetics; HIV-1 gp120; HIV (Viruses); gp120-CD4D12; gp120-M9; HIV Vaccine Design; gp120; Highly Active Anti-Retroviral Therapy (HAART); Molecular Biology

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

APA (6th Edition):

Chakraborty, K. (2005). gp120 Immunogen Design And Characterization. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/1499

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):

Chakraborty, Kausik. “gp120 Immunogen Design And Characterization.” 2005. Thesis, Indian Institute of Science. Accessed January 19, 2020. http://hdl.handle.net/2005/1499.

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

MLA Handbook (7th Edition):

Chakraborty, Kausik. “gp120 Immunogen Design And Characterization.” 2005. Web. 19 Jan 2020.

Vancouver:

Chakraborty K. gp120 Immunogen Design And Characterization. [Internet] [Thesis]. Indian Institute of Science; 2005. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/2005/1499.

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

Council of Science Editors:

Chakraborty K. gp120 Immunogen Design And Characterization. [Thesis]. Indian Institute of Science; 2005. Available from: http://hdl.handle.net/2005/1499

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


University of Saskatchewan

22. Zhang, Chenhong. An improved fully connected hidden Markov model for rational vaccine design.

Degree: 2005, University of Saskatchewan

 Large-scale, in vitro vaccine screening is an expensive and slow process, while rational vaccine design is faster and cheaper. As opposed to the emperical ways… (more)

Subjects/Keywords: heuristic matrix initialization; fully connected hidden markov model; rational vaccine design

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APA (6th Edition):

Zhang, C. (2005). An improved fully connected hidden Markov model for rational vaccine design. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/etd-02232005-121948

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):

Zhang, Chenhong. “An improved fully connected hidden Markov model for rational vaccine design.” 2005. Thesis, University of Saskatchewan. Accessed January 19, 2020. http://hdl.handle.net/10388/etd-02232005-121948.

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

MLA Handbook (7th Edition):

Zhang, Chenhong. “An improved fully connected hidden Markov model for rational vaccine design.” 2005. Web. 19 Jan 2020.

Vancouver:

Zhang C. An improved fully connected hidden Markov model for rational vaccine design. [Internet] [Thesis]. University of Saskatchewan; 2005. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/10388/etd-02232005-121948.

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

Council of Science Editors:

Zhang C. An improved fully connected hidden Markov model for rational vaccine design. [Thesis]. University of Saskatchewan; 2005. Available from: http://hdl.handle.net/10388/etd-02232005-121948

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


Queensland University of Technology

23. Armitage, Charles William. The role of immunoglobulins and their transporters in urogenital Chlamydial infections.

Degree: 2012, Queensland University of Technology

 Chlamydia trachomatis infections of the male and female reproductive tracts are the world's leading sexually transmitted bacterial disease, and can lead to damaging pathology, scarring… (more)

Subjects/Keywords: Chlamydia trachomatis; Chlamydia muridarum; immunoglobulin (Ig); IgG; IgA; neonatal Fc receptor (FcRn); polymeric immunoglobulin receptor (pIgR); reproductive tract; vaccine design; MOMP; IncA; CPAF

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APA (6th Edition):

Armitage, C. W. (2012). The role of immunoglobulins and their transporters in urogenital Chlamydial infections. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/63693/

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):

Armitage, Charles William. “The role of immunoglobulins and their transporters in urogenital Chlamydial infections.” 2012. Thesis, Queensland University of Technology. Accessed January 19, 2020. https://eprints.qut.edu.au/63693/.

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

MLA Handbook (7th Edition):

Armitage, Charles William. “The role of immunoglobulins and their transporters in urogenital Chlamydial infections.” 2012. Web. 19 Jan 2020.

Vancouver:

Armitage CW. The role of immunoglobulins and their transporters in urogenital Chlamydial infections. [Internet] [Thesis]. Queensland University of Technology; 2012. [cited 2020 Jan 19]. Available from: https://eprints.qut.edu.au/63693/.

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

Council of Science Editors:

Armitage CW. The role of immunoglobulins and their transporters in urogenital Chlamydial infections. [Thesis]. Queensland University of Technology; 2012. Available from: https://eprints.qut.edu.au/63693/

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

24. Carrico, Christopher T D. Understanding and Manipulating Anti-HIV Antibody Responses via Structural Methods.

Degree: PhD, 2014, University of Washington

 Anti-HIV antibody responses offer one of very few potential routes towards a protective HIV vaccine; structural biochemistry methods such as crystallography and computational modeling can… (more)

Subjects/Keywords: Crystallography; HIV; Protein Design; Protein Structure; Vaccine; Biochemistry; biological chemistry

…Focused HIV Vaccine Design Given the immense human and social costs associated with HIV, and the… …their desired, Env-like conformations is a key advance in vaccine design. I performed… …ramifications for vaccine design are explored. Appendix 1: Glycan Masking of Plasmodium vivax Duffy… …mentioned, much of the current work in the HIV vaccine design field focuses on engineering the… …in vaccine design, particularly in the case of heavily glycosylated viral envelope proteins… 

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

APA (6th Edition):

Carrico, C. T. D. (2014). Understanding and Manipulating Anti-HIV Antibody Responses via Structural Methods. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/25107

Chicago Manual of Style (16th Edition):

Carrico, Christopher T D. “Understanding and Manipulating Anti-HIV Antibody Responses via Structural Methods.” 2014. Doctoral Dissertation, University of Washington. Accessed January 19, 2020. http://hdl.handle.net/1773/25107.

MLA Handbook (7th Edition):

Carrico, Christopher T D. “Understanding and Manipulating Anti-HIV Antibody Responses via Structural Methods.” 2014. Web. 19 Jan 2020.

Vancouver:

Carrico CTD. Understanding and Manipulating Anti-HIV Antibody Responses via Structural Methods. [Internet] [Doctoral dissertation]. University of Washington; 2014. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/1773/25107.

Council of Science Editors:

Carrico CTD. Understanding and Manipulating Anti-HIV Antibody Responses via Structural Methods. [Doctoral Dissertation]. University of Washington; 2014. Available from: http://hdl.handle.net/1773/25107


Iowa State University

25. El-manzalawy, Yasser Mohamed. Machine learning approaches for epitope prediction.

Degree: 2008, Iowa State University

 The identification and characterization of epitopes in antigenic sequences is critical for understanding disease pathogenesis, for identifying potential autoantigens, and for designing vaccines and immune-based… (more)

Subjects/Keywords: epitope prediction; immunoinformatics; machine learning; scoring matrices; sequence analysis; vaccine design; Computer Sciences

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APA (6th Edition):

El-manzalawy, Y. M. (2008). Machine learning approaches for epitope prediction. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/10908

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):

El-manzalawy, Yasser Mohamed. “Machine learning approaches for epitope prediction.” 2008. Thesis, Iowa State University. Accessed January 19, 2020. https://lib.dr.iastate.edu/etd/10908.

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

MLA Handbook (7th Edition):

El-manzalawy, Yasser Mohamed. “Machine learning approaches for epitope prediction.” 2008. Web. 19 Jan 2020.

Vancouver:

El-manzalawy YM. Machine learning approaches for epitope prediction. [Internet] [Thesis]. Iowa State University; 2008. [cited 2020 Jan 19]. Available from: https://lib.dr.iastate.edu/etd/10908.

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

Council of Science Editors:

El-manzalawy YM. Machine learning approaches for epitope prediction. [Thesis]. Iowa State University; 2008. Available from: https://lib.dr.iastate.edu/etd/10908

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


Indian Institute of Science

26. Bhattacharyya, Sanchari. Targeting The CD4 Biniding Site In HIV-1 Immunogen Design.

Degree: 2012, Indian Institute of Science

 Over three decades have passed since the discovery of HIV-1, yet an AIDS vaccine remains elusive. The envelope glycoprotein of HIV-1 gp120, is the most… (more)

Subjects/Keywords: HIV-1 Immunogens; HIV (Human Immuno Deficiency Virus); Retrovirus; HIV-1 Immunogens - Design; Disulfide Mutants; B12 Binding Site Immunogen; HIV-1 Vaccine Design; HIV-1 gp120 Immunogens; gp120 Proteins; HIV-1 Immunogen Design; Biochemistry

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

APA (6th Edition):

Bhattacharyya, S. (2012). Targeting The CD4 Biniding Site In HIV-1 Immunogen Design. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/2586

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):

Bhattacharyya, Sanchari. “Targeting The CD4 Biniding Site In HIV-1 Immunogen Design.” 2012. Thesis, Indian Institute of Science. Accessed January 19, 2020. http://hdl.handle.net/2005/2586.

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

MLA Handbook (7th Edition):

Bhattacharyya, Sanchari. “Targeting The CD4 Biniding Site In HIV-1 Immunogen Design.” 2012. Web. 19 Jan 2020.

Vancouver:

Bhattacharyya S. Targeting The CD4 Biniding Site In HIV-1 Immunogen Design. [Internet] [Thesis]. Indian Institute of Science; 2012. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/2005/2586.

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

Council of Science Editors:

Bhattacharyya S. Targeting The CD4 Biniding Site In HIV-1 Immunogen Design. [Thesis]. Indian Institute of Science; 2012. Available from: http://hdl.handle.net/2005/2586

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


University of Oxford

27. Schiffner, Torben. Refocusing antibody responses by chemical modification of vaccine antigens.

Degree: PhD, 2014, University of Oxford

 The envelope glycoprotein (Env) of Human Immunodeficiency Virus 1 (HIV-1) has developed several immune-evasion mechanisms to avoid the induction of neutralising antibodies, including immunodominant non-neutralising… (more)

Subjects/Keywords: 616.07; Glycobiology; Biochemistry; Biology; Medical sciences; Biology (medical sciences); Disease prevention; Immunology; Infectious diseases; Pathology; Vaccinology; Viruses; Vaccine Design; Antigenicity; Immunogenicity; Envelope Glycoproteins; Neutralizing Antibody; Glycosylation; Protein Modifications; Glycoconjugates; Chemical Cross-linking

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APA (6th Edition):

Schiffner, T. (2014). Refocusing antibody responses by chemical modification of vaccine antigens. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:2b2cac0f-6be3-4f91-96e5-9888e02780d4 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635304

Chicago Manual of Style (16th Edition):

Schiffner, Torben. “Refocusing antibody responses by chemical modification of vaccine antigens.” 2014. Doctoral Dissertation, University of Oxford. Accessed January 19, 2020. http://ora.ox.ac.uk/objects/uuid:2b2cac0f-6be3-4f91-96e5-9888e02780d4 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635304.

MLA Handbook (7th Edition):

Schiffner, Torben. “Refocusing antibody responses by chemical modification of vaccine antigens.” 2014. Web. 19 Jan 2020.

Vancouver:

Schiffner T. Refocusing antibody responses by chemical modification of vaccine antigens. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2020 Jan 19]. Available from: http://ora.ox.ac.uk/objects/uuid:2b2cac0f-6be3-4f91-96e5-9888e02780d4 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635304.

Council of Science Editors:

Schiffner T. Refocusing antibody responses by chemical modification of vaccine antigens. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:2b2cac0f-6be3-4f91-96e5-9888e02780d4 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635304


The Ohio State University

28. Sundaram, Roshni. Evaluation of T-cell and B-cell epitopes and design of multivalent vaccines against HTLV-1 diseases.

Degree: PhD, Microbiology, 2003, The Ohio State University

 Human T-cell lymphotropic virus type I (HTLV-1) is a C type retrovirus that is the causative agent of an aggressive T-cell malignancy, adult T-cell leukemia/lymphoma… (more)

Subjects/Keywords: peptide vaccine design; multivalent; HLA-A2.1 transgenic mice; antibodies; coiled coil; B-cell epitopes; T-cell epitopes

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

APA (6th Edition):

Sundaram, R. (2003). Evaluation of T-cell and B-cell epitopes and design of multivalent vaccines against HTLV-1 diseases. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1054054439

Chicago Manual of Style (16th Edition):

Sundaram, Roshni. “Evaluation of T-cell and B-cell epitopes and design of multivalent vaccines against HTLV-1 diseases.” 2003. Doctoral Dissertation, The Ohio State University. Accessed January 19, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1054054439.

MLA Handbook (7th Edition):

Sundaram, Roshni. “Evaluation of T-cell and B-cell epitopes and design of multivalent vaccines against HTLV-1 diseases.” 2003. Web. 19 Jan 2020.

Vancouver:

Sundaram R. Evaluation of T-cell and B-cell epitopes and design of multivalent vaccines against HTLV-1 diseases. [Internet] [Doctoral dissertation]. The Ohio State University; 2003. [cited 2020 Jan 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1054054439.

Council of Science Editors:

Sundaram R. Evaluation of T-cell and B-cell epitopes and design of multivalent vaccines against HTLV-1 diseases. [Doctoral Dissertation]. The Ohio State University; 2003. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1054054439

29. Richert, Laura. Trial design and analysis of endpoints in HIV vaccine trials : Schéma d’étude et analyses des données des essais vaccinaux du VIH.

Degree: Docteur es, Sociétés, Politique, Santé publique. Santé Publique. Epidémiologie, 2013, Université de Bordeaux Segalen

Des données complexes sont fréquentes dans les essais cliniques récents et nécessitent des méthodes statistiques adaptées. La recherche vaccinale du VIH est un exemple d’un… (more)

Subjects/Keywords: Vaccin contre le VIH; Marqueurs d’immunogénicité; Données multidimensionnelles; Variables résumées multivariées; Critères de jugement; Schémas d’essais cliniques optimisés; HIV vaccine; Immunogenicity markers; Multidimensional data; Multivariate summary measures; Endpoint definitions; Optimized clinical trial design

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

APA (6th Edition):

Richert, L. (2013). Trial design and analysis of endpoints in HIV vaccine trials : Schéma d’étude et analyses des données des essais vaccinaux du VIH. (Doctoral Dissertation). Université de Bordeaux Segalen. Retrieved from http://www.theses.fr/2013BOR22048

Chicago Manual of Style (16th Edition):

Richert, Laura. “Trial design and analysis of endpoints in HIV vaccine trials : Schéma d’étude et analyses des données des essais vaccinaux du VIH.” 2013. Doctoral Dissertation, Université de Bordeaux Segalen. Accessed January 19, 2020. http://www.theses.fr/2013BOR22048.

MLA Handbook (7th Edition):

Richert, Laura. “Trial design and analysis of endpoints in HIV vaccine trials : Schéma d’étude et analyses des données des essais vaccinaux du VIH.” 2013. Web. 19 Jan 2020.

Vancouver:

Richert L. Trial design and analysis of endpoints in HIV vaccine trials : Schéma d’étude et analyses des données des essais vaccinaux du VIH. [Internet] [Doctoral dissertation]. Université de Bordeaux Segalen; 2013. [cited 2020 Jan 19]. Available from: http://www.theses.fr/2013BOR22048.

Council of Science Editors:

Richert L. Trial design and analysis of endpoints in HIV vaccine trials : Schéma d’étude et analyses des données des essais vaccinaux du VIH. [Doctoral Dissertation]. Université de Bordeaux Segalen; 2013. Available from: http://www.theses.fr/2013BOR22048


University of Queensland

30. Doan, Thanh Tam. Structural presentation of influenza epitopes on modular virus-like particles.

Degree: Australian Institute for Bioengineering and Nanotechnology, 2018, University of Queensland

Subjects/Keywords: Virus-like particle; Influenza; Peptide antigen; Structural presentation; Vaccine design; 0904 Chemical Engineering; 1004 Medical Biotechnology

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

APA (6th Edition):

Doan, T. T. (2018). Structural presentation of influenza epitopes on modular virus-like particles. (Thesis). University of Queensland. Retrieved from http://espace.library.uq.edu.au/view/UQ:7

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):

Doan, Thanh Tam. “Structural presentation of influenza epitopes on modular virus-like particles.” 2018. Thesis, University of Queensland. Accessed January 19, 2020. http://espace.library.uq.edu.au/view/UQ:7.

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

MLA Handbook (7th Edition):

Doan, Thanh Tam. “Structural presentation of influenza epitopes on modular virus-like particles.” 2018. Web. 19 Jan 2020.

Vancouver:

Doan TT. Structural presentation of influenza epitopes on modular virus-like particles. [Internet] [Thesis]. University of Queensland; 2018. [cited 2020 Jan 19]. Available from: http://espace.library.uq.edu.au/view/UQ:7.

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

Council of Science Editors:

Doan TT. Structural presentation of influenza epitopes on modular virus-like particles. [Thesis]. University of Queensland; 2018. Available from: http://espace.library.uq.edu.au/view/UQ:7

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

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