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You searched for subject:(Virus like particles). Showing records 1 – 30 of 69 total matches.

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University of Otago

1. Win, Stephanie Joy. Inducing Anti-Tumor Immune Responses with Antigen Conjugated Virus-Like Particles .

Degree: 2011, University of Otago

Virus-like particles (VLP) have been shown to be useful nanoscale platforms in a diverse range of applications including their use as vaccines. They can act… (more)

Subjects/Keywords: Virus-Like Particles; Immunotherapy

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APA (6th Edition):

Win, S. J. (2011). Inducing Anti-Tumor Immune Responses with Antigen Conjugated Virus-Like Particles . (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/1733

Chicago Manual of Style (16th Edition):

Win, Stephanie Joy. “Inducing Anti-Tumor Immune Responses with Antigen Conjugated Virus-Like Particles .” 2011. Doctoral Dissertation, University of Otago. Accessed February 17, 2020. http://hdl.handle.net/10523/1733.

MLA Handbook (7th Edition):

Win, Stephanie Joy. “Inducing Anti-Tumor Immune Responses with Antigen Conjugated Virus-Like Particles .” 2011. Web. 17 Feb 2020.

Vancouver:

Win SJ. Inducing Anti-Tumor Immune Responses with Antigen Conjugated Virus-Like Particles . [Internet] [Doctoral dissertation]. University of Otago; 2011. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/10523/1733.

Council of Science Editors:

Win SJ. Inducing Anti-Tumor Immune Responses with Antigen Conjugated Virus-Like Particles . [Doctoral Dissertation]. University of Otago; 2011. Available from: http://hdl.handle.net/10523/1733


University of New Mexico

2. Tyler, Mitchell. Development of HPV next-generation virus-like particle vaccines that are cross-protective.

Degree: Biomedical Sciences Graduate Program, 2014, University of New Mexico

Virus-like particles (VLPs) comprised of viral structural proteins that self-assemble into particles resembling the native virion represent a relatively novel vaccine development strategy. Both safe… (more)

Subjects/Keywords: virus-like particles; human papillomavirus; vaccines

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APA (6th Edition):

Tyler, M. (2014). Development of HPV next-generation virus-like particle vaccines that are cross-protective. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/147

Chicago Manual of Style (16th Edition):

Tyler, Mitchell. “Development of HPV next-generation virus-like particle vaccines that are cross-protective.” 2014. Doctoral Dissertation, University of New Mexico. Accessed February 17, 2020. https://digitalrepository.unm.edu/biom_etds/147.

MLA Handbook (7th Edition):

Tyler, Mitchell. “Development of HPV next-generation virus-like particle vaccines that are cross-protective.” 2014. Web. 17 Feb 2020.

Vancouver:

Tyler M. Development of HPV next-generation virus-like particle vaccines that are cross-protective. [Internet] [Doctoral dissertation]. University of New Mexico; 2014. [cited 2020 Feb 17]. Available from: https://digitalrepository.unm.edu/biom_etds/147.

Council of Science Editors:

Tyler M. Development of HPV next-generation virus-like particle vaccines that are cross-protective. [Doctoral Dissertation]. University of New Mexico; 2014. Available from: https://digitalrepository.unm.edu/biom_etds/147


University of New Mexico

3. Medford, Alex. The Generation and Immunogenicity of PP7 Virus-Like Particles Displaying Target Antigens.

Degree: Biomedical Sciences Graduate Program, 2010, University of New Mexico

 The immunogenicity of an antigen can be increased by displaying it in a highly dense, multivalent context, such as on the surface of a virus(more)

Subjects/Keywords: VLPs; bacteriophage; Virus like particles; PP7

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APA (6th Edition):

Medford, A. (2010). The Generation and Immunogenicity of PP7 Virus-Like Particles Displaying Target Antigens. (Masters Thesis). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/8

Chicago Manual of Style (16th Edition):

Medford, Alex. “The Generation and Immunogenicity of PP7 Virus-Like Particles Displaying Target Antigens.” 2010. Masters Thesis, University of New Mexico. Accessed February 17, 2020. https://digitalrepository.unm.edu/biom_etds/8.

MLA Handbook (7th Edition):

Medford, Alex. “The Generation and Immunogenicity of PP7 Virus-Like Particles Displaying Target Antigens.” 2010. Web. 17 Feb 2020.

Vancouver:

Medford A. The Generation and Immunogenicity of PP7 Virus-Like Particles Displaying Target Antigens. [Internet] [Masters thesis]. University of New Mexico; 2010. [cited 2020 Feb 17]. Available from: https://digitalrepository.unm.edu/biom_etds/8.

Council of Science Editors:

Medford A. The Generation and Immunogenicity of PP7 Virus-Like Particles Displaying Target Antigens. [Masters Thesis]. University of New Mexico; 2010. Available from: https://digitalrepository.unm.edu/biom_etds/8


University of Otago

4. Scullion, Sarah Louise. Investigating Cytotoxic T cell Responses to RHDV Virus-like Particles .

Degree: 2012, University of Otago

 Immunotherapies prime cells of the immune system to generate an appropriate response against a specific target. One area of Immunotherapeutic research is the development of… (more)

Subjects/Keywords: Immunology; Cytotoxic T cells; Virus-like particles

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APA (6th Edition):

Scullion, S. L. (2012). Investigating Cytotoxic T cell Responses to RHDV Virus-like Particles . (Masters Thesis). University of Otago. Retrieved from http://hdl.handle.net/10523/2402

Chicago Manual of Style (16th Edition):

Scullion, Sarah Louise. “Investigating Cytotoxic T cell Responses to RHDV Virus-like Particles .” 2012. Masters Thesis, University of Otago. Accessed February 17, 2020. http://hdl.handle.net/10523/2402.

MLA Handbook (7th Edition):

Scullion, Sarah Louise. “Investigating Cytotoxic T cell Responses to RHDV Virus-like Particles .” 2012. Web. 17 Feb 2020.

Vancouver:

Scullion SL. Investigating Cytotoxic T cell Responses to RHDV Virus-like Particles . [Internet] [Masters thesis]. University of Otago; 2012. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/10523/2402.

Council of Science Editors:

Scullion SL. Investigating Cytotoxic T cell Responses to RHDV Virus-like Particles . [Masters Thesis]. University of Otago; 2012. Available from: http://hdl.handle.net/10523/2402


NSYSU

5. LIN, CHIA-YU. The Study on the Shell-Domain Structure of Capsid Protein from Dragon Grouper Betanodavirus.

Degree: Master, Marine Biotechnology and Resources, 2017, NSYSU

 Nodaviridae is divided into Alphanodavirus and Betanodavirus. Alphanodavirus and Betanodavirus infect insects and fish, respectively. The infection of Betanodavirus have been demonstrated the cause of… (more)

Subjects/Keywords: capsid protein; virus-like particles; crystallization; Dragon grouper nervous necrosis virus

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APA (6th Edition):

LIN, C. (2017). The Study on the Shell-Domain Structure of Capsid Protein from Dragon Grouper Betanodavirus. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0513117-121727

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):

LIN, CHIA-YU. “The Study on the Shell-Domain Structure of Capsid Protein from Dragon Grouper Betanodavirus.” 2017. Thesis, NSYSU. Accessed February 17, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0513117-121727.

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

MLA Handbook (7th Edition):

LIN, CHIA-YU. “The Study on the Shell-Domain Structure of Capsid Protein from Dragon Grouper Betanodavirus.” 2017. Web. 17 Feb 2020.

Vancouver:

LIN C. The Study on the Shell-Domain Structure of Capsid Protein from Dragon Grouper Betanodavirus. [Internet] [Thesis]. NSYSU; 2017. [cited 2020 Feb 17]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0513117-121727.

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

Council of Science Editors:

LIN C. The Study on the Shell-Domain Structure of Capsid Protein from Dragon Grouper Betanodavirus. [Thesis]. NSYSU; 2017. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0513117-121727

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


NSYSU

6. Liu, Yu-Ting. The Surface Recognition on the VLPs of Dragon Grouper Nervous Necrosis Virus by its Antibodies.

Degree: Master, Marine Biotechnology and Resources, 2011, NSYSU

 Grouper in Taiwan is of high value, but nervous necrosis virus infection causes 100% mortality. Our laboratory had developed a good expression system to produce… (more)

Subjects/Keywords: grouper nervous necrosis virus; monoclone antibody; virus-like particles; hybridoma; ascites

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APA (6th Edition):

Liu, Y. (2011). The Surface Recognition on the VLPs of Dragon Grouper Nervous Necrosis Virus by its Antibodies. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0909111-114035

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):

Liu, Yu-Ting. “The Surface Recognition on the VLPs of Dragon Grouper Nervous Necrosis Virus by its Antibodies.” 2011. Thesis, NSYSU. Accessed February 17, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0909111-114035.

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

MLA Handbook (7th Edition):

Liu, Yu-Ting. “The Surface Recognition on the VLPs of Dragon Grouper Nervous Necrosis Virus by its Antibodies.” 2011. Web. 17 Feb 2020.

Vancouver:

Liu Y. The Surface Recognition on the VLPs of Dragon Grouper Nervous Necrosis Virus by its Antibodies. [Internet] [Thesis]. NSYSU; 2011. [cited 2020 Feb 17]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0909111-114035.

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

Council of Science Editors:

Liu Y. The Surface Recognition on the VLPs of Dragon Grouper Nervous Necrosis Virus by its Antibodies. [Thesis]. NSYSU; 2011. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0909111-114035

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


NSYSU

7. Lin, Yen-fu. The Studies on Crystal Stability of Virus-like Particle from Dragon Grouper Betanodavirus.

Degree: Master, Marine Biotechnology and Resources, 2015, NSYSU

 Dragon grouper nervous necrosis virus (DGNNV), a betanodavirus, is the cause of viral nervous necrosis in dragon grouper (Epinephelus lanceolatus). In larvae and juveniles, mortality… (more)

Subjects/Keywords: virus-like particles; Dragon grouper nervous necrosis virus; crystallization; cross-linking

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APA (6th Edition):

Lin, Y. (2015). The Studies on Crystal Stability of Virus-like Particle from Dragon Grouper Betanodavirus. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0529115-094154

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):

Lin, Yen-fu. “The Studies on Crystal Stability of Virus-like Particle from Dragon Grouper Betanodavirus.” 2015. Thesis, NSYSU. Accessed February 17, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0529115-094154.

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

MLA Handbook (7th Edition):

Lin, Yen-fu. “The Studies on Crystal Stability of Virus-like Particle from Dragon Grouper Betanodavirus.” 2015. Web. 17 Feb 2020.

Vancouver:

Lin Y. The Studies on Crystal Stability of Virus-like Particle from Dragon Grouper Betanodavirus. [Internet] [Thesis]. NSYSU; 2015. [cited 2020 Feb 17]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0529115-094154.

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

Council of Science Editors:

Lin Y. The Studies on Crystal Stability of Virus-like Particle from Dragon Grouper Betanodavirus. [Thesis]. NSYSU; 2015. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0529115-094154

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


University of Vienna

8. Kappelmann, Melanie. Virus-like particles of Pseudoalteromonas marina and their possible medical significance.

Degree: 2010, University of Vienna

Virus- like- particles (VLPs) sind Membranvesikel welche von einigen marinen Bakterien spontan während des bakteriellen Wachstums abgegeben werden. In dieser Arbeit wurde die VLP- Produktion… (more)

Subjects/Keywords: 42.13 Molekularbiologie; 42.30 Mikrobiologie; Pseudoalteromonas marina / "Virus- like- Particles" / antibakterielle Aktivität; Pseudoalteromonas marina / virus- like- particles / antibacterial activity

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APA (6th Edition):

Kappelmann, M. (2010). Virus-like particles of Pseudoalteromonas marina and their possible medical significance. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/11729/

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):

Kappelmann, Melanie. “Virus-like particles of Pseudoalteromonas marina and their possible medical significance.” 2010. Thesis, University of Vienna. Accessed February 17, 2020. http://othes.univie.ac.at/11729/.

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

MLA Handbook (7th Edition):

Kappelmann, Melanie. “Virus-like particles of Pseudoalteromonas marina and their possible medical significance.” 2010. Web. 17 Feb 2020.

Vancouver:

Kappelmann M. Virus-like particles of Pseudoalteromonas marina and their possible medical significance. [Internet] [Thesis]. University of Vienna; 2010. [cited 2020 Feb 17]. Available from: http://othes.univie.ac.at/11729/.

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

Council of Science Editors:

Kappelmann M. Virus-like particles of Pseudoalteromonas marina and their possible medical significance. [Thesis]. University of Vienna; 2010. Available from: http://othes.univie.ac.at/11729/

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


NSYSU

9. Pang , Hao-Han. Using Multifunctional Qβ Virus-Like Particles for RNAi and Reducing Temozolomide Resistance in Brain Tumor.

Degree: Master, Institute of Medical Science and Technology, 2017, NSYSU

 Introducion Brain tumour is one of the most lethal cancers due to difficulties of delivering therapeutic agents across blood-brain barrier (BBB) and serious side effect.… (more)

Subjects/Keywords: drug resistance; RNAi; VLPs; Virus-like particles; Brain Tumor; Temozolomide

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APA (6th Edition):

Pang , H. (2017). Using Multifunctional Qβ Virus-Like Particles for RNAi and Reducing Temozolomide Resistance in Brain Tumor. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0723117-132050

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):

Pang , Hao-Han. “Using Multifunctional Qβ Virus-Like Particles for RNAi and Reducing Temozolomide Resistance in Brain Tumor.” 2017. Thesis, NSYSU. Accessed February 17, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0723117-132050.

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

MLA Handbook (7th Edition):

Pang , Hao-Han. “Using Multifunctional Qβ Virus-Like Particles for RNAi and Reducing Temozolomide Resistance in Brain Tumor.” 2017. Web. 17 Feb 2020.

Vancouver:

Pang H. Using Multifunctional Qβ Virus-Like Particles for RNAi and Reducing Temozolomide Resistance in Brain Tumor. [Internet] [Thesis]. NSYSU; 2017. [cited 2020 Feb 17]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0723117-132050.

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

Council of Science Editors:

Pang H. Using Multifunctional Qβ Virus-Like Particles for RNAi and Reducing Temozolomide Resistance in Brain Tumor. [Thesis]. NSYSU; 2017. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0723117-132050

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


University of New Mexico

10. Hunter, Zoe. Induction of mucosal immunity using virus-like particle based vaccines.

Degree: Biomedical Sciences Graduate Program, 2011, University of New Mexico

 Many viral structural proteins are capable of spontaneously self-assembling into structures that resemble virus particles. These structures, called virus-like particles (VLPs), have multivalent, highly repetitive… (more)

Subjects/Keywords: virus-like particles; CCR5; mucosal immunity; vaccine; HPV16 L2

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APA (6th Edition):

Hunter, Z. (2011). Induction of mucosal immunity using virus-like particle based vaccines. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/31

Chicago Manual of Style (16th Edition):

Hunter, Zoe. “Induction of mucosal immunity using virus-like particle based vaccines.” 2011. Doctoral Dissertation, University of New Mexico. Accessed February 17, 2020. https://digitalrepository.unm.edu/biom_etds/31.

MLA Handbook (7th Edition):

Hunter, Zoe. “Induction of mucosal immunity using virus-like particle based vaccines.” 2011. Web. 17 Feb 2020.

Vancouver:

Hunter Z. Induction of mucosal immunity using virus-like particle based vaccines. [Internet] [Doctoral dissertation]. University of New Mexico; 2011. [cited 2020 Feb 17]. Available from: https://digitalrepository.unm.edu/biom_etds/31.

Council of Science Editors:

Hunter Z. Induction of mucosal immunity using virus-like particle based vaccines. [Doctoral Dissertation]. University of New Mexico; 2011. Available from: https://digitalrepository.unm.edu/biom_etds/31


University of Kansas

11. Kissmann, Julian Michael. The Application of Empirical Phase Diagrams to the Biophysical Characterization and Stabilization of Viral Vaccine Candidates.

Degree: PhD, Pharmaceutical Chemistry, 2010, University of Kansas

 This dissertation describes the application of a composite biophysical approach to the characterization and stabilization of viruses and virus-like particles for vaccine purposes. Spectroscopic, calorimetric,… (more)

Subjects/Keywords: Pharmaceutical chemistry; Formulation; Influenza; Measles; Stabilization; Vaccine; Virus-like particles

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APA (6th Edition):

Kissmann, J. M. (2010). The Application of Empirical Phase Diagrams to the Biophysical Characterization and Stabilization of Viral Vaccine Candidates. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/6299

Chicago Manual of Style (16th Edition):

Kissmann, Julian Michael. “The Application of Empirical Phase Diagrams to the Biophysical Characterization and Stabilization of Viral Vaccine Candidates.” 2010. Doctoral Dissertation, University of Kansas. Accessed February 17, 2020. http://hdl.handle.net/1808/6299.

MLA Handbook (7th Edition):

Kissmann, Julian Michael. “The Application of Empirical Phase Diagrams to the Biophysical Characterization and Stabilization of Viral Vaccine Candidates.” 2010. Web. 17 Feb 2020.

Vancouver:

Kissmann JM. The Application of Empirical Phase Diagrams to the Biophysical Characterization and Stabilization of Viral Vaccine Candidates. [Internet] [Doctoral dissertation]. University of Kansas; 2010. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/1808/6299.

Council of Science Editors:

Kissmann JM. The Application of Empirical Phase Diagrams to the Biophysical Characterization and Stabilization of Viral Vaccine Candidates. [Doctoral Dissertation]. University of Kansas; 2010. Available from: http://hdl.handle.net/1808/6299


Universidade Nova

12. Velez, André Filipe Marques. Produção de Virus Like Particles (VLPs) do vírus Chikungunya (CHIKV).

Degree: 2012, Universidade Nova

 O vírus Chikungunya (CHIKV) é um alfavírus, transmitido por mosquitos, que causa infecção aguda no Homem caracterizada por febre, mialgia e poliartrite dolorosa e incapacitante… (more)

Subjects/Keywords: Virus-like particles; vírus chikungunya; pLEXm; transfecção com polietilenimina

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APA (6th Edition):

Velez, A. F. M. (2012). Produção de Virus Like Particles (VLPs) do vírus Chikungunya (CHIKV). (Thesis). Universidade Nova. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/19201

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):

Velez, André Filipe Marques. “Produção de Virus Like Particles (VLPs) do vírus Chikungunya (CHIKV).” 2012. Thesis, Universidade Nova. Accessed February 17, 2020. http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/19201.

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

MLA Handbook (7th Edition):

Velez, André Filipe Marques. “Produção de Virus Like Particles (VLPs) do vírus Chikungunya (CHIKV).” 2012. Web. 17 Feb 2020.

Vancouver:

Velez AFM. Produção de Virus Like Particles (VLPs) do vírus Chikungunya (CHIKV). [Internet] [Thesis]. Universidade Nova; 2012. [cited 2020 Feb 17]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/19201.

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

Council of Science Editors:

Velez AFM. Produção de Virus Like Particles (VLPs) do vírus Chikungunya (CHIKV). [Thesis]. Universidade Nova; 2012. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/19201

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


UCLA

13. Biddlecome, Adam Min. In Vitro-Reconstituted Virus-like-particle Delivery of Self-Amplifying RNA Genes.

Degree: Biochemistry, Molecular and Structural Biology, 2019, UCLA

 The delivery of RNA genes has great potential in a range of therapeutic applications. A couple of main limitations for RNA-based therapies include its vulnerability… (more)

Subjects/Keywords: Biochemistry; dendritic cell activation; self-replicating; virus-like particles

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APA (6th Edition):

Biddlecome, A. M. (2019). In Vitro-Reconstituted Virus-like-particle Delivery of Self-Amplifying RNA Genes. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/8g9539bf

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):

Biddlecome, Adam Min. “In Vitro-Reconstituted Virus-like-particle Delivery of Self-Amplifying RNA Genes.” 2019. Thesis, UCLA. Accessed February 17, 2020. http://www.escholarship.org/uc/item/8g9539bf.

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

MLA Handbook (7th Edition):

Biddlecome, Adam Min. “In Vitro-Reconstituted Virus-like-particle Delivery of Self-Amplifying RNA Genes.” 2019. Web. 17 Feb 2020.

Vancouver:

Biddlecome AM. In Vitro-Reconstituted Virus-like-particle Delivery of Self-Amplifying RNA Genes. [Internet] [Thesis]. UCLA; 2019. [cited 2020 Feb 17]. Available from: http://www.escholarship.org/uc/item/8g9539bf.

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

Council of Science Editors:

Biddlecome AM. In Vitro-Reconstituted Virus-like-particle Delivery of Self-Amplifying RNA Genes. [Thesis]. UCLA; 2019. Available from: http://www.escholarship.org/uc/item/8g9539bf

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


KTH

14. Höglund, Beatrice. Inverkan av positionella effekter, promotorer och terminatorer på proteinexpression, exemplifierat med multiprotein influenza-viruslika partiklar.

Degree: Biotechnology (BIO), 2014, KTH

  The existing seasonal influenza vaccine does not provide broad long-term protection against seasonal influenza and must be remanufactured yearly due to frequens mutations and… (more)

Subjects/Keywords: Virus-like particles; influenza vaccine; baculovirus; insect cell culture; recombinant production

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APA (6th Edition):

Höglund, B. (2014). Inverkan av positionella effekter, promotorer och terminatorer på proteinexpression, exemplifierat med multiprotein influenza-viruslika partiklar. (Thesis). KTH. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-163673

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):

Höglund, Beatrice. “Inverkan av positionella effekter, promotorer och terminatorer på proteinexpression, exemplifierat med multiprotein influenza-viruslika partiklar.” 2014. Thesis, KTH. Accessed February 17, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-163673.

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

MLA Handbook (7th Edition):

Höglund, Beatrice. “Inverkan av positionella effekter, promotorer och terminatorer på proteinexpression, exemplifierat med multiprotein influenza-viruslika partiklar.” 2014. Web. 17 Feb 2020.

Vancouver:

Höglund B. Inverkan av positionella effekter, promotorer och terminatorer på proteinexpression, exemplifierat med multiprotein influenza-viruslika partiklar. [Internet] [Thesis]. KTH; 2014. [cited 2020 Feb 17]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-163673.

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

Council of Science Editors:

Höglund B. Inverkan av positionella effekter, promotorer och terminatorer på proteinexpression, exemplifierat med multiprotein influenza-viruslika partiklar. [Thesis]. KTH; 2014. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-163673

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


Georgia Tech

15. Fang, Po-Yu. Using QB VLPS to package, protect, and deliver in vivo produced RNAS.

Degree: PhD, Chemistry and Biochemistry, 2016, Georgia Tech

 This project focuses on Using Qβ VLPs to package, protect, and deliver recombinantly produced RNAs. The ultimate goal is to develop an RNA interference (RNAi)… (more)

Subjects/Keywords: Virus-like particles; RNAi; Gene regulation; RNA protection

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APA (6th Edition):

Fang, P. (2016). Using QB VLPS to package, protect, and deliver in vivo produced RNAS. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58592

Chicago Manual of Style (16th Edition):

Fang, Po-Yu. “Using QB VLPS to package, protect, and deliver in vivo produced RNAS.” 2016. Doctoral Dissertation, Georgia Tech. Accessed February 17, 2020. http://hdl.handle.net/1853/58592.

MLA Handbook (7th Edition):

Fang, Po-Yu. “Using QB VLPS to package, protect, and deliver in vivo produced RNAS.” 2016. Web. 17 Feb 2020.

Vancouver:

Fang P. Using QB VLPS to package, protect, and deliver in vivo produced RNAS. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/1853/58592.

Council of Science Editors:

Fang P. Using QB VLPS to package, protect, and deliver in vivo produced RNAS. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/58592


University of Technology, Sydney

16. Banik, GR. Ultrastructural description of Dientamoeba fragilis and a new viral-like particle.

Degree: 2014, University of Technology, Sydney

 Dientamoeba fragilis is a trichomonad protozoan found in the gastrointestinal tract of humans and is implicated as a cause of diarrhoeal disease. Despite its widespread… (more)

Subjects/Keywords: Dientamoeba fragilis.; Trichomonadida.; Virus- like particles.; Gastrointestinal diseases.

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APA (6th Edition):

Banik, G. (2014). Ultrastructural description of Dientamoeba fragilis and a new viral-like particle. (Thesis). University of Technology, Sydney. Retrieved from http://hdl.handle.net/10453/28061

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):

Banik, GR. “Ultrastructural description of Dientamoeba fragilis and a new viral-like particle.” 2014. Thesis, University of Technology, Sydney. Accessed February 17, 2020. http://hdl.handle.net/10453/28061.

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

MLA Handbook (7th Edition):

Banik, GR. “Ultrastructural description of Dientamoeba fragilis and a new viral-like particle.” 2014. Web. 17 Feb 2020.

Vancouver:

Banik G. Ultrastructural description of Dientamoeba fragilis and a new viral-like particle. [Internet] [Thesis]. University of Technology, Sydney; 2014. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/10453/28061.

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

Council of Science Editors:

Banik G. Ultrastructural description of Dientamoeba fragilis and a new viral-like particle. [Thesis]. University of Technology, Sydney; 2014. Available from: http://hdl.handle.net/10453/28061

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


NSYSU

17. Luo, Yu-Chun. Crystallization and X-ray diffraction of virus-like particles from dragon grouper betanodavirus.

Degree: PhD, Marine Biotechnology and Resources, 2014, NSYSU

 The Betanodaviruses caused nerve necrosis in more than 40 species. The clinical symptoms of virus-infected fish include abnormal movement and darkness in body color, with… (more)

Subjects/Keywords: virus-like particles; dragon grouper nervous necrosis virus (DGNNV); crystallization; vapor diffusion method

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APA (6th Edition):

Luo, Y. (2014). Crystallization and X-ray diffraction of virus-like particles from dragon grouper betanodavirus. (Doctoral Dissertation). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1028114-123106

Chicago Manual of Style (16th Edition):

Luo, Yu-Chun. “Crystallization and X-ray diffraction of virus-like particles from dragon grouper betanodavirus.” 2014. Doctoral Dissertation, NSYSU. Accessed February 17, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1028114-123106.

MLA Handbook (7th Edition):

Luo, Yu-Chun. “Crystallization and X-ray diffraction of virus-like particles from dragon grouper betanodavirus.” 2014. Web. 17 Feb 2020.

Vancouver:

Luo Y. Crystallization and X-ray diffraction of virus-like particles from dragon grouper betanodavirus. [Internet] [Doctoral dissertation]. NSYSU; 2014. [cited 2020 Feb 17]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1028114-123106.

Council of Science Editors:

Luo Y. Crystallization and X-ray diffraction of virus-like particles from dragon grouper betanodavirus. [Doctoral Dissertation]. NSYSU; 2014. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1028114-123106


University of Melbourne

18. Samanthi Narasimhulu, Vani Geetha. Studies on the role of the membrane proximal ectodomain region (MPER) of HIV-1 gp41 in virus transmission and viral glycoprotein antigenic structure.

Degree: 2017, University of Melbourne

 The trimeric HIV-1 envelope glycoprotein (Env) complex, gp120-gp41, is the primary viral structure that elicits neutralizing antibodies. The isolation of broadly neutralizing monoclonal antibodies (bNAbs)… (more)

Subjects/Keywords: HIV; MPER; virus like particles; cell-cell virus transmission; domain swap; transmitted/founder

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APA (6th Edition):

Samanthi Narasimhulu, V. G. (2017). Studies on the role of the membrane proximal ectodomain region (MPER) of HIV-1 gp41 in virus transmission and viral glycoprotein antigenic structure. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/124270

Chicago Manual of Style (16th Edition):

Samanthi Narasimhulu, Vani Geetha. “Studies on the role of the membrane proximal ectodomain region (MPER) of HIV-1 gp41 in virus transmission and viral glycoprotein antigenic structure.” 2017. Doctoral Dissertation, University of Melbourne. Accessed February 17, 2020. http://hdl.handle.net/11343/124270.

MLA Handbook (7th Edition):

Samanthi Narasimhulu, Vani Geetha. “Studies on the role of the membrane proximal ectodomain region (MPER) of HIV-1 gp41 in virus transmission and viral glycoprotein antigenic structure.” 2017. Web. 17 Feb 2020.

Vancouver:

Samanthi Narasimhulu VG. Studies on the role of the membrane proximal ectodomain region (MPER) of HIV-1 gp41 in virus transmission and viral glycoprotein antigenic structure. [Internet] [Doctoral dissertation]. University of Melbourne; 2017. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/11343/124270.

Council of Science Editors:

Samanthi Narasimhulu VG. Studies on the role of the membrane proximal ectodomain region (MPER) of HIV-1 gp41 in virus transmission and viral glycoprotein antigenic structure. [Doctoral Dissertation]. University of Melbourne; 2017. Available from: http://hdl.handle.net/11343/124270


Georgia State University

19. Hwang, Hye Suk. EFFICACY AND SAFETY OF VIRUS LIKE PARTICLE VACCINES AGAINST RESPIRATORY SYNCYTIAL VIRUS IN MOUSE AND COTTON RAT MODELS.

Degree: PhD, Biology, 2016, Georgia State University

  Respiratory syncytial virus (RSV) is a major cause of infectious lower respiratory disease in infants and the elderly. Vaccine-enhanced respiratory disease (ERD) has been… (more)

Subjects/Keywords: Respiratory Syncytial Virus; Virus like particles; Protection; histopathology; T helper type-1 immune responses

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APA (6th Edition):

Hwang, H. S. (2016). EFFICACY AND SAFETY OF VIRUS LIKE PARTICLE VACCINES AGAINST RESPIRATORY SYNCYTIAL VIRUS IN MOUSE AND COTTON RAT MODELS. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/biology_diss/180

Chicago Manual of Style (16th Edition):

Hwang, Hye Suk. “EFFICACY AND SAFETY OF VIRUS LIKE PARTICLE VACCINES AGAINST RESPIRATORY SYNCYTIAL VIRUS IN MOUSE AND COTTON RAT MODELS.” 2016. Doctoral Dissertation, Georgia State University. Accessed February 17, 2020. https://scholarworks.gsu.edu/biology_diss/180.

MLA Handbook (7th Edition):

Hwang, Hye Suk. “EFFICACY AND SAFETY OF VIRUS LIKE PARTICLE VACCINES AGAINST RESPIRATORY SYNCYTIAL VIRUS IN MOUSE AND COTTON RAT MODELS.” 2016. Web. 17 Feb 2020.

Vancouver:

Hwang HS. EFFICACY AND SAFETY OF VIRUS LIKE PARTICLE VACCINES AGAINST RESPIRATORY SYNCYTIAL VIRUS IN MOUSE AND COTTON RAT MODELS. [Internet] [Doctoral dissertation]. Georgia State University; 2016. [cited 2020 Feb 17]. Available from: https://scholarworks.gsu.edu/biology_diss/180.

Council of Science Editors:

Hwang HS. EFFICACY AND SAFETY OF VIRUS LIKE PARTICLE VACCINES AGAINST RESPIRATORY SYNCYTIAL VIRUS IN MOUSE AND COTTON RAT MODELS. [Doctoral Dissertation]. Georgia State University; 2016. Available from: https://scholarworks.gsu.edu/biology_diss/180


Freie Universität Berlin

20. Pfaff, Kerstin. Hepatitis C virus pseudo-particles and their suitability in virological diagnostics.

Degree: 2012, Freie Universität Berlin

 Hepatitis B and C viral infections are worldwide a formidable medical problem and a threat to global health. In particular the infection with HCV is… (more)

Subjects/Keywords: Hepatitis C virus; virus neutralization; virus-like particles; 600 Technik, Medizin, angewandte Wissenschaften::630 Landwirtschaft::630 Landwirtschaft und verwandte Bereiche

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APA (6th Edition):

Pfaff, K. (2012). Hepatitis C virus pseudo-particles and their suitability in virological diagnostics. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/10432

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):

Pfaff, Kerstin. “Hepatitis C virus pseudo-particles and their suitability in virological diagnostics.” 2012. Thesis, Freie Universität Berlin. Accessed February 17, 2020. https://refubium.fu-berlin.de/handle/fub188/10432.

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

MLA Handbook (7th Edition):

Pfaff, Kerstin. “Hepatitis C virus pseudo-particles and their suitability in virological diagnostics.” 2012. Web. 17 Feb 2020.

Vancouver:

Pfaff K. Hepatitis C virus pseudo-particles and their suitability in virological diagnostics. [Internet] [Thesis]. Freie Universität Berlin; 2012. [cited 2020 Feb 17]. Available from: https://refubium.fu-berlin.de/handle/fub188/10432.

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

Council of Science Editors:

Pfaff K. Hepatitis C virus pseudo-particles and their suitability in virological diagnostics. [Thesis]. Freie Universität Berlin; 2012. Available from: https://refubium.fu-berlin.de/handle/fub188/10432

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


University of California – Berkeley

21. Aanei, Ioana Laura. Protein-based Nanoparticles for Imaging and Drug Delivery Applications.

Degree: Chemistry, 2016, University of California – Berkeley

 Protein cage architectures such as viral capsids, heat shock proteins, and ferritins are naturally occurring nanoscale structures with exquisite homogeneity and stability. This dissertation work… (more)

Subjects/Keywords: Chemistry; Atherosclerosis; Cancer Imaging; Drug delivery; Nanoparticle; Protein scaffold; Virus-like particles

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APA (6th Edition):

Aanei, I. L. (2016). Protein-based Nanoparticles for Imaging and Drug Delivery Applications. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/95r130rb

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):

Aanei, Ioana Laura. “Protein-based Nanoparticles for Imaging and Drug Delivery Applications.” 2016. Thesis, University of California – Berkeley. Accessed February 17, 2020. http://www.escholarship.org/uc/item/95r130rb.

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

MLA Handbook (7th Edition):

Aanei, Ioana Laura. “Protein-based Nanoparticles for Imaging and Drug Delivery Applications.” 2016. Web. 17 Feb 2020.

Vancouver:

Aanei IL. Protein-based Nanoparticles for Imaging and Drug Delivery Applications. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2020 Feb 17]. Available from: http://www.escholarship.org/uc/item/95r130rb.

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

Council of Science Editors:

Aanei IL. Protein-based Nanoparticles for Imaging and Drug Delivery Applications. [Thesis]. University of California – Berkeley; 2016. Available from: http://www.escholarship.org/uc/item/95r130rb

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

22. Guerreiro, Sara Isabel Domingos. Vacinação contra papilomavírus: uma revisão.

Degree: 2016, RCAAP

Dissertação para obtenção do grau de Mestre no Instituto Superior de Ciências da Saúde Egas Moniz

Ao longo dos últimos anos, e devido ao avanço… (more)

Subjects/Keywords: Papilomavírus humano; Infeções; Cancro do colo do útero; Vacinação; Virus-like particles

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APA (6th Edition):

Guerreiro, S. I. D. (2016). Vacinação contra papilomavírus: uma revisão. (Thesis). RCAAP. Retrieved from https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/17674

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):

Guerreiro, Sara Isabel Domingos. “Vacinação contra papilomavírus: uma revisão.” 2016. Thesis, RCAAP. Accessed February 17, 2020. https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/17674.

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

MLA Handbook (7th Edition):

Guerreiro, Sara Isabel Domingos. “Vacinação contra papilomavírus: uma revisão.” 2016. Web. 17 Feb 2020.

Vancouver:

Guerreiro SID. Vacinação contra papilomavírus: uma revisão. [Internet] [Thesis]. RCAAP; 2016. [cited 2020 Feb 17]. Available from: https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/17674.

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

Council of Science Editors:

Guerreiro SID. Vacinação contra papilomavírus: uma revisão. [Thesis]. RCAAP; 2016. Available from: https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/17674

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


Virginia Tech

23. Lohneis, Taylor Paige. Consistent Fabrication of Ultrasmall PLGA Nanoparticles and their Potential Biomedical Applications.

Degree: MS, Biological Systems Engineering, 2019, Virginia Tech

 Nanotechnology, the manipulation of materials on an atomic or molecular scale, and its potential for biomedical applications has become an area of increasing interest over… (more)

Subjects/Keywords: PLGA nanoparticles; ultrasmall size; nanoprecipitation; virus-like particles; protein-based vaccines; protein assembly; VLP scaffold

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APA (6th Edition):

Lohneis, T. P. (2019). Consistent Fabrication of Ultrasmall PLGA Nanoparticles and their Potential Biomedical Applications. (Masters Thesis). Virginia Tech. Retrieved from http://hdl.handle.net/10919/95943

Chicago Manual of Style (16th Edition):

Lohneis, Taylor Paige. “Consistent Fabrication of Ultrasmall PLGA Nanoparticles and their Potential Biomedical Applications.” 2019. Masters Thesis, Virginia Tech. Accessed February 17, 2020. http://hdl.handle.net/10919/95943.

MLA Handbook (7th Edition):

Lohneis, Taylor Paige. “Consistent Fabrication of Ultrasmall PLGA Nanoparticles and their Potential Biomedical Applications.” 2019. Web. 17 Feb 2020.

Vancouver:

Lohneis TP. Consistent Fabrication of Ultrasmall PLGA Nanoparticles and their Potential Biomedical Applications. [Internet] [Masters thesis]. Virginia Tech; 2019. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/10919/95943.

Council of Science Editors:

Lohneis TP. Consistent Fabrication of Ultrasmall PLGA Nanoparticles and their Potential Biomedical Applications. [Masters Thesis]. Virginia Tech; 2019. Available from: http://hdl.handle.net/10919/95943


University of Georgia

24. Saha, Agniva. Discovery of a novel restriction factor encoded by the retrotransposon ty1 in saccharomyces cerevisiae.

Degree: PhD, Biochemistry and Molecular Biology, 2017, University of Georgia

 Ty1 is the most active long terminal repeat (LTR) retrotransposon in Saccharomyces cerevisiae and resembles retroviruses in genome organization and replication mechanisms. Ty1 encodes the… (more)

Subjects/Keywords: Retrotransposon; retrovirus; LTR; virus-like particles; restriction factor; copy number control; genome defense

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APA (6th Edition):

Saha, A. (2017). Discovery of a novel restriction factor encoded by the retrotransposon ty1 in saccharomyces cerevisiae. (Doctoral Dissertation). University of Georgia. Retrieved from http://hdl.handle.net/10724/37489

Chicago Manual of Style (16th Edition):

Saha, Agniva. “Discovery of a novel restriction factor encoded by the retrotransposon ty1 in saccharomyces cerevisiae.” 2017. Doctoral Dissertation, University of Georgia. Accessed February 17, 2020. http://hdl.handle.net/10724/37489.

MLA Handbook (7th Edition):

Saha, Agniva. “Discovery of a novel restriction factor encoded by the retrotransposon ty1 in saccharomyces cerevisiae.” 2017. Web. 17 Feb 2020.

Vancouver:

Saha A. Discovery of a novel restriction factor encoded by the retrotransposon ty1 in saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of Georgia; 2017. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/10724/37489.

Council of Science Editors:

Saha A. Discovery of a novel restriction factor encoded by the retrotransposon ty1 in saccharomyces cerevisiae. [Doctoral Dissertation]. University of Georgia; 2017. Available from: http://hdl.handle.net/10724/37489


Arizona State University

25. Meador, Lydia Rebecca. Searching for an HIV Vaccine: A Heterologous Prime-boost System using Replicating Vaccinia Virus and Plant-produced Virus-like Particles.

Degree: Biological Design, 2016, Arizona State University

 The HIV-1 pandemic continues to cause millions of new infections and AIDS-related deaths each year, and a majority of these occur in regions of the… (more)

Subjects/Keywords: Virology; Immunology; Molecular biology; HIV; innate immunity; plant biotechnology; vaccine; viral vectors; virus-like particles

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APA (6th Edition):

Meador, L. R. (2016). Searching for an HIV Vaccine: A Heterologous Prime-boost System using Replicating Vaccinia Virus and Plant-produced Virus-like Particles. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/40210

Chicago Manual of Style (16th Edition):

Meador, Lydia Rebecca. “Searching for an HIV Vaccine: A Heterologous Prime-boost System using Replicating Vaccinia Virus and Plant-produced Virus-like Particles.” 2016. Doctoral Dissertation, Arizona State University. Accessed February 17, 2020. http://repository.asu.edu/items/40210.

MLA Handbook (7th Edition):

Meador, Lydia Rebecca. “Searching for an HIV Vaccine: A Heterologous Prime-boost System using Replicating Vaccinia Virus and Plant-produced Virus-like Particles.” 2016. Web. 17 Feb 2020.

Vancouver:

Meador LR. Searching for an HIV Vaccine: A Heterologous Prime-boost System using Replicating Vaccinia Virus and Plant-produced Virus-like Particles. [Internet] [Doctoral dissertation]. Arizona State University; 2016. [cited 2020 Feb 17]. Available from: http://repository.asu.edu/items/40210.

Council of Science Editors:

Meador LR. Searching for an HIV Vaccine: A Heterologous Prime-boost System using Replicating Vaccinia Virus and Plant-produced Virus-like Particles. [Doctoral Dissertation]. Arizona State University; 2016. Available from: http://repository.asu.edu/items/40210


Georgia Tech

26. 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 February 17, 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. 17 Feb 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 Feb 17]. 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

27. CORDEIRO, Marcelo Nazário. Clonagem molecular e expressão em Pichia pastoris do gene L1 de papilomavírus bovino tipo 2 .

Degree: 2010, Universidade Federal de Pernambuco

 Os papilomavírus são um grupo de pequenos vírus DNA dupla fita caracterizado por induzir a formação de lesões que, normalmente, são benignas e podem regredir… (more)

Subjects/Keywords: Papilomavírus; Vetor de expressão; Proteína L1; Vírus-like particles; Papillomavirus; Expression vector; L1 protein; Virus-like particle; Leveduras

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APA (6th Edition):

CORDEIRO, M. N. (2010). Clonagem molecular e expressão em Pichia pastoris do gene L1 de papilomavírus bovino tipo 2 . (Thesis). Universidade Federal de Pernambuco. Retrieved from http://repositorio.ufpe.br/handle/123456789/18479

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):

CORDEIRO, Marcelo Nazário. “Clonagem molecular e expressão em Pichia pastoris do gene L1 de papilomavírus bovino tipo 2 .” 2010. Thesis, Universidade Federal de Pernambuco. Accessed February 17, 2020. http://repositorio.ufpe.br/handle/123456789/18479.

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

MLA Handbook (7th Edition):

CORDEIRO, Marcelo Nazário. “Clonagem molecular e expressão em Pichia pastoris do gene L1 de papilomavírus bovino tipo 2 .” 2010. Web. 17 Feb 2020.

Vancouver:

CORDEIRO MN. Clonagem molecular e expressão em Pichia pastoris do gene L1 de papilomavírus bovino tipo 2 . [Internet] [Thesis]. Universidade Federal de Pernambuco; 2010. [cited 2020 Feb 17]. Available from: http://repositorio.ufpe.br/handle/123456789/18479.

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

Council of Science Editors:

CORDEIRO MN. Clonagem molecular e expressão em Pichia pastoris do gene L1 de papilomavírus bovino tipo 2 . [Thesis]. Universidade Federal de Pernambuco; 2010. Available from: http://repositorio.ufpe.br/handle/123456789/18479

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


University of Rochester

28. Lifson, Mark. Nanoparticles as tools for nano-/micro- biosystems.

Degree: PhD, 2015, University of Rochester

 Nanoscale interactions are at the heart of almost all biochemical processes, and understanding them using biosensors is an important and challenging problem in biology and… (more)

Subjects/Keywords: Photonic crystal; Arrayed imaging reflectometry; Hydrogel nanoparticles; PNIPAM; Biosensing; Virus-like particles; VLP; Human papilloma virus; HPV; Label-free

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

APA (6th Edition):

Lifson, M. (2015). Nanoparticles as tools for nano-/micro- biosystems. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/29252

Chicago Manual of Style (16th Edition):

Lifson, Mark. “Nanoparticles as tools for nano-/micro- biosystems.” 2015. Doctoral Dissertation, University of Rochester. Accessed February 17, 2020. http://hdl.handle.net/1802/29252.

MLA Handbook (7th Edition):

Lifson, Mark. “Nanoparticles as tools for nano-/micro- biosystems.” 2015. Web. 17 Feb 2020.

Vancouver:

Lifson M. Nanoparticles as tools for nano-/micro- biosystems. [Internet] [Doctoral dissertation]. University of Rochester; 2015. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/1802/29252.

Council of Science Editors:

Lifson M. Nanoparticles as tools for nano-/micro- biosystems. [Doctoral Dissertation]. University of Rochester; 2015. Available from: http://hdl.handle.net/1802/29252


Rice University

29. Guu, Tom Sheng-yaw. Structure of the hepatitis E virus-like particle suggests me chanisms for virus assembly and receptor binding.

Degree: PhD, Natural Sciences, 2009, Rice University

 This thesis reports the atomic structure of the Hepatitis E virus (HEV) in the form of a virus-like particle (VLP). HEV is a small, non-enveloped… (more)

Subjects/Keywords: Molecular biology; Virology; Immunology; Health and environmental sciences; Biological sciences; Capsid proteins; Hepatitis; Hepatitis E virus; Linear domains; Receptor binding; Virus assembly; Virus-like particles

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

APA (6th Edition):

Guu, T. S. (2009). Structure of the hepatitis E virus-like particle suggests me chanisms for virus assembly and receptor binding. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/103720

Chicago Manual of Style (16th Edition):

Guu, Tom Sheng-yaw. “Structure of the hepatitis E virus-like particle suggests me chanisms for virus assembly and receptor binding.” 2009. Doctoral Dissertation, Rice University. Accessed February 17, 2020. http://hdl.handle.net/1911/103720.

MLA Handbook (7th Edition):

Guu, Tom Sheng-yaw. “Structure of the hepatitis E virus-like particle suggests me chanisms for virus assembly and receptor binding.” 2009. Web. 17 Feb 2020.

Vancouver:

Guu TS. Structure of the hepatitis E virus-like particle suggests me chanisms for virus assembly and receptor binding. [Internet] [Doctoral dissertation]. Rice University; 2009. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/1911/103720.

Council of Science Editors:

Guu TS. Structure of the hepatitis E virus-like particle suggests me chanisms for virus assembly and receptor binding. [Doctoral Dissertation]. Rice University; 2009. Available from: http://hdl.handle.net/1911/103720


Universitat Autònoma de Barcelona

30. Cervera Garcia, Laura. Strategies for improving production levels of HIV-1 VLPs by transient transfection of HEK 293 suspension cultures.

Degree: Departament de Química, 2015, Universitat Autònoma de Barcelona

Virus-like particles (VLPs) offer great potential as candidates for new vaccine production. In this work, the development and optimization of an HIV-1 Gag VLP production… (more)

Subjects/Keywords: Transfecció transitòria; Transfección transitoria; Transient transfection; Partícules similars a virus; Partículas como virus; Virus-like particles; Cél·lules de mamífer; Células de mamífero; Mammalian cell culture; Ciències Experimentals; 573

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

APA (6th Edition):

Cervera Garcia, L. (2015). Strategies for improving production levels of HIV-1 VLPs by transient transfection of HEK 293 suspension cultures. (Thesis). Universitat Autònoma de Barcelona. Retrieved from http://hdl.handle.net/10803/289626

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):

Cervera Garcia, Laura. “Strategies for improving production levels of HIV-1 VLPs by transient transfection of HEK 293 suspension cultures.” 2015. Thesis, Universitat Autònoma de Barcelona. Accessed February 17, 2020. http://hdl.handle.net/10803/289626.

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

MLA Handbook (7th Edition):

Cervera Garcia, Laura. “Strategies for improving production levels of HIV-1 VLPs by transient transfection of HEK 293 suspension cultures.” 2015. Web. 17 Feb 2020.

Vancouver:

Cervera Garcia L. Strategies for improving production levels of HIV-1 VLPs by transient transfection of HEK 293 suspension cultures. [Internet] [Thesis]. Universitat Autònoma de Barcelona; 2015. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/10803/289626.

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

Council of Science Editors:

Cervera Garcia L. Strategies for improving production levels of HIV-1 VLPs by transient transfection of HEK 293 suspension cultures. [Thesis]. Universitat Autònoma de Barcelona; 2015. Available from: http://hdl.handle.net/10803/289626

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

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