Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for +publisher:"University of New Mexico" +contributor:("Peabody, David"). Showing records 1 – 13 of 13 total matches.

Search Limiters

Last 2 Years | English Only

No search limiters apply to these results.

▼ Search Limiters


University of New Mexico

1. Subhadra, Bobban. Paratransgenic control of vibriosis in shrimp aquaculture.

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

 Infectious diseases are an increasing threat to shrimp farming industries worldwide and account for nearly $3 billion of annual economic loss. The need to devise… (more)

Subjects/Keywords: "Paratransgenesis; Shrimp diseases; Aquaculture"

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Subhadra, B. (2011). Paratransgenic control of vibriosis in shrimp aquaculture. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/38

Chicago Manual of Style (16th Edition):

Subhadra, Bobban. “Paratransgenic control of vibriosis in shrimp aquaculture.” 2011. Doctoral Dissertation, University of New Mexico. Accessed May 22, 2019. https://digitalrepository.unm.edu/biom_etds/38.

MLA Handbook (7th Edition):

Subhadra, Bobban. “Paratransgenic control of vibriosis in shrimp aquaculture.” 2011. Web. 22 May 2019.

Vancouver:

Subhadra B. Paratransgenic control of vibriosis in shrimp aquaculture. [Internet] [Doctoral dissertation]. University of New Mexico; 2011. [cited 2019 May 22]. Available from: https://digitalrepository.unm.edu/biom_etds/38.

Council of Science Editors:

Subhadra B. Paratransgenic control of vibriosis in shrimp aquaculture. [Doctoral Dissertation]. University of New Mexico; 2011. Available from: https://digitalrepository.unm.edu/biom_etds/38


University of New Mexico

2. Dowling, James. Progeny Release of Species B Human Adenoviruses Is Not Mediated By Early Region 3 Proteins 20.1K, 20.5k, and 10.9k.

Degree: Biomedical Sciences Graduate Program, 2013, University of New Mexico

 The early region 3 (E3) of the human adenovirus (HAdV) genome encodes proteins that regulate the host immune response to viral infection. The E3 region… (more)

Subjects/Keywords: adenovirus; human adenovirus; early region 3; E3; E3-20.1K; E3-20.5K; E3-10.9K; species b human adenovirus

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Dowling, J. (2013). Progeny Release of Species B Human Adenoviruses Is Not Mediated By Early Region 3 Proteins 20.1K, 20.5k, and 10.9k. (Masters Thesis). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/69

Chicago Manual of Style (16th Edition):

Dowling, James. “Progeny Release of Species B Human Adenoviruses Is Not Mediated By Early Region 3 Proteins 20.1K, 20.5k, and 10.9k.” 2013. Masters Thesis, University of New Mexico. Accessed May 22, 2019. https://digitalrepository.unm.edu/biom_etds/69.

MLA Handbook (7th Edition):

Dowling, James. “Progeny Release of Species B Human Adenoviruses Is Not Mediated By Early Region 3 Proteins 20.1K, 20.5k, and 10.9k.” 2013. Web. 22 May 2019.

Vancouver:

Dowling J. Progeny Release of Species B Human Adenoviruses Is Not Mediated By Early Region 3 Proteins 20.1K, 20.5k, and 10.9k. [Internet] [Masters thesis]. University of New Mexico; 2013. [cited 2019 May 22]. Available from: https://digitalrepository.unm.edu/biom_etds/69.

Council of Science Editors:

Dowling J. Progeny Release of Species B Human Adenoviruses Is Not Mediated By Early Region 3 Proteins 20.1K, 20.5k, and 10.9k. [Masters Thesis]. University of New Mexico; 2013. Available from: https://digitalrepository.unm.edu/biom_etds/69


University of New Mexico

3. Rogers, Jason Hugh. Development of CD19 binding reagents for targeted nanoparticles.

Degree: Biomedical Sciences Graduate Program, 2013, University of New Mexico

 B-cell malignancies like Acute Lymphoblastic Leukemia (B-ALL), which often have high numbers of malignant cells in circulation in the blood would be an excellent model… (more)

Subjects/Keywords: leukemia; CD19; nanoparticle; phage display; ScFv antibody

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Rogers, J. H. (2013). Development of CD19 binding reagents for targeted nanoparticles. (Masters Thesis). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/73

Chicago Manual of Style (16th Edition):

Rogers, Jason Hugh. “Development of CD19 binding reagents for targeted nanoparticles.” 2013. Masters Thesis, University of New Mexico. Accessed May 22, 2019. https://digitalrepository.unm.edu/biom_etds/73.

MLA Handbook (7th Edition):

Rogers, Jason Hugh. “Development of CD19 binding reagents for targeted nanoparticles.” 2013. Web. 22 May 2019.

Vancouver:

Rogers JH. Development of CD19 binding reagents for targeted nanoparticles. [Internet] [Masters thesis]. University of New Mexico; 2013. [cited 2019 May 22]. Available from: https://digitalrepository.unm.edu/biom_etds/73.

Council of Science Editors:

Rogers JH. Development of CD19 binding reagents for targeted nanoparticles. [Masters Thesis]. University of New Mexico; 2013. Available from: https://digitalrepository.unm.edu/biom_etds/73


University of New Mexico

4. Kivitz, Michael. Investigation Into The Early Events Of Epithelial Wound Healing and HPV16 Infection.

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

 HPV16 infection evidently occurs within wounded epithelial tissue, but the cellular and molecular events that culminate in infection establishment remain poorly understood. While HPV is… (more)

Subjects/Keywords: HPV16; Wound Healing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kivitz, M. (2014). Investigation Into The Early Events Of Epithelial Wound Healing and HPV16 Infection. (Masters Thesis). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/90

Chicago Manual of Style (16th Edition):

Kivitz, Michael. “Investigation Into The Early Events Of Epithelial Wound Healing and HPV16 Infection.” 2014. Masters Thesis, University of New Mexico. Accessed May 22, 2019. https://digitalrepository.unm.edu/biom_etds/90.

MLA Handbook (7th Edition):

Kivitz, Michael. “Investigation Into The Early Events Of Epithelial Wound Healing and HPV16 Infection.” 2014. Web. 22 May 2019.

Vancouver:

Kivitz M. Investigation Into The Early Events Of Epithelial Wound Healing and HPV16 Infection. [Internet] [Masters thesis]. University of New Mexico; 2014. [cited 2019 May 22]. Available from: https://digitalrepository.unm.edu/biom_etds/90.

Council of Science Editors:

Kivitz M. Investigation Into The Early Events Of Epithelial Wound Healing and HPV16 Infection. [Masters Thesis]. University of New Mexico; 2014. Available from: https://digitalrepository.unm.edu/biom_etds/90


University of New Mexico

5. Crossey, Erin. Bacteriophage virus-like particles as vaccine platforms : from heart disease to malaria.

Degree: Biomedical Sciences Graduate Program, 2016, University of New Mexico

 Virus-like particles (VLPs) make excellent vaccines. They are non-infectious, often easy to produce in bacterial expression systems, and highly immunogenic. The latter feature is granted… (more)

Subjects/Keywords: virus-like particle; bacteriophage; affinity selection; vaccine; malaria; hypercholesterolemia

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Crossey, E. (2016). Bacteriophage virus-like particles as vaccine platforms : from heart disease to malaria. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/119

Chicago Manual of Style (16th Edition):

Crossey, Erin. “Bacteriophage virus-like particles as vaccine platforms : from heart disease to malaria.” 2016. Doctoral Dissertation, University of New Mexico. Accessed May 22, 2019. https://digitalrepository.unm.edu/biom_etds/119.

MLA Handbook (7th Edition):

Crossey, Erin. “Bacteriophage virus-like particles as vaccine platforms : from heart disease to malaria.” 2016. Web. 22 May 2019.

Vancouver:

Crossey E. Bacteriophage virus-like particles as vaccine platforms : from heart disease to malaria. [Internet] [Doctoral dissertation]. University of New Mexico; 2016. [cited 2019 May 22]. Available from: https://digitalrepository.unm.edu/biom_etds/119.

Council of Science Editors:

Crossey E. Bacteriophage virus-like particles as vaccine platforms : from heart disease to malaria. [Doctoral Dissertation]. University of New Mexico; 2016. Available from: https://digitalrepository.unm.edu/biom_etds/119


University of New Mexico

6. Lino, Christopher Andrew. DISPLAY OF PEPTIDES AND SINGLE-CHAIN ANTIBODIES ON BACTERIOPHAGE MS2 VIRUS-LIKE PARTICLES.

Degree: Biomedical Sciences Graduate Program, 2013, University of New Mexico

 Phage display is a powerful technology for selection of novel binding functions from large populations of peptide or antibody fragments. From a sufficiently complex library,… (more)

Subjects/Keywords: VLP; MS2; scFv; Bacteriophage; Affinity Selection; Random Libraries

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lino, C. A. (2013). DISPLAY OF PEPTIDES AND SINGLE-CHAIN ANTIBODIES ON BACTERIOPHAGE MS2 VIRUS-LIKE PARTICLES. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/135

Chicago Manual of Style (16th Edition):

Lino, Christopher Andrew. “DISPLAY OF PEPTIDES AND SINGLE-CHAIN ANTIBODIES ON BACTERIOPHAGE MS2 VIRUS-LIKE PARTICLES.” 2013. Doctoral Dissertation, University of New Mexico. Accessed May 22, 2019. https://digitalrepository.unm.edu/biom_etds/135.

MLA Handbook (7th Edition):

Lino, Christopher Andrew. “DISPLAY OF PEPTIDES AND SINGLE-CHAIN ANTIBODIES ON BACTERIOPHAGE MS2 VIRUS-LIKE PARTICLES.” 2013. Web. 22 May 2019.

Vancouver:

Lino CA. DISPLAY OF PEPTIDES AND SINGLE-CHAIN ANTIBODIES ON BACTERIOPHAGE MS2 VIRUS-LIKE PARTICLES. [Internet] [Doctoral dissertation]. University of New Mexico; 2013. [cited 2019 May 22]. Available from: https://digitalrepository.unm.edu/biom_etds/135.

Council of Science Editors:

Lino CA. DISPLAY OF PEPTIDES AND SINGLE-CHAIN ANTIBODIES ON BACTERIOPHAGE MS2 VIRUS-LIKE PARTICLES. [Doctoral Dissertation]. University of New Mexico; 2013. Available from: https://digitalrepository.unm.edu/biom_etds/135


University of New Mexico

7. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 May 22, 2019. 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. 22 May 2019.

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 2019 May 22]. 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

8. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 May 22, 2019. 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. 22 May 2019.

Vancouver:

Medford A. The Generation and Immunogenicity of PP7 Virus-Like Particles Displaying Target Antigens. [Internet] [Masters thesis]. University of New Mexico; 2010. [cited 2019 May 22]. 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 New Mexico

9. Ashley, Carlee. Development of novel bio/nano interfaces for materials science and biomedical applications.

Degree: Chemical and Biological Engineering, 2011, University of New Mexico

  Virus-like particles (VLPs) of MS2 bacteriophage possess a variety of characteristics that enable their use in biomedical and materials science applications. MS2 VLPs are… (more)

Subjects/Keywords: targeted delivery; cancer; bio-nano interfaces; self-assembly; virus-like particles; phage display; GISAXS; Nanoparticles.; Drug carriers (Pharmacy); Drug targeting.; Cancer – Treatment.; Nanostructured materials.; Solar cells.; Chemical Engineering

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ashley, C. (2011). Development of novel bio/nano interfaces for materials science and biomedical applications. (Doctoral Dissertation). University of New Mexico. Retrieved from http://hdl.handle.net/1928/12979

Chicago Manual of Style (16th Edition):

Ashley, Carlee. “Development of novel bio/nano interfaces for materials science and biomedical applications.” 2011. Doctoral Dissertation, University of New Mexico. Accessed May 22, 2019. http://hdl.handle.net/1928/12979.

MLA Handbook (7th Edition):

Ashley, Carlee. “Development of novel bio/nano interfaces for materials science and biomedical applications.” 2011. Web. 22 May 2019.

Vancouver:

Ashley C. Development of novel bio/nano interfaces for materials science and biomedical applications. [Internet] [Doctoral dissertation]. University of New Mexico; 2011. [cited 2019 May 22]. Available from: http://hdl.handle.net/1928/12979.

Council of Science Editors:

Ashley C. Development of novel bio/nano interfaces for materials science and biomedical applications. [Doctoral Dissertation]. University of New Mexico; 2011. Available from: http://hdl.handle.net/1928/12979


University of New Mexico

10. Jordan, Sheldon Keith. Engineering RNA phage MS2 virus-like particles for peptide display.

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

 Phage display is a powerful and versatile technology that enables the selection of novel binding functions from large populations of randomly generated peptide sequences. Random… (more)

Subjects/Keywords: bacteriophage MS2; virus-like particle; nanoscience; biomedical engineering; phage display; phage vaccine

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Jordan, S. K. (2010). Engineering RNA phage MS2 virus-like particles for peptide display. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/13

Chicago Manual of Style (16th Edition):

Jordan, Sheldon Keith. “Engineering RNA phage MS2 virus-like particles for peptide display.” 2010. Doctoral Dissertation, University of New Mexico. Accessed May 22, 2019. https://digitalrepository.unm.edu/biom_etds/13.

MLA Handbook (7th Edition):

Jordan, Sheldon Keith. “Engineering RNA phage MS2 virus-like particles for peptide display.” 2010. Web. 22 May 2019.

Vancouver:

Jordan SK. Engineering RNA phage MS2 virus-like particles for peptide display. [Internet] [Doctoral dissertation]. University of New Mexico; 2010. [cited 2019 May 22]. Available from: https://digitalrepository.unm.edu/biom_etds/13.

Council of Science Editors:

Jordan SK. Engineering RNA phage MS2 virus-like particles for peptide display. [Doctoral Dissertation]. University of New Mexico; 2010. Available from: https://digitalrepository.unm.edu/biom_etds/13


University of New Mexico

11. Frietze, Kathryn Marie. Characterization of subspecies B1 human adenovirus ORF E3-10.9K.

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

 Subspecies B1 human adenoviruses (HAdVs) are important causes of acute respiratory disease in pediatric and military recruit populations. Although extensive epidemiological data document the genetic… (more)

Subjects/Keywords: Adenovirus; Early region 3; B1 human adenovirus; viroporin

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Frietze, K. M. (2010). Characterization of subspecies B1 human adenovirus ORF E3-10.9K. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/24

Chicago Manual of Style (16th Edition):

Frietze, Kathryn Marie. “Characterization of subspecies B1 human adenovirus ORF E3-10.9K.” 2010. Doctoral Dissertation, University of New Mexico. Accessed May 22, 2019. https://digitalrepository.unm.edu/biom_etds/24.

MLA Handbook (7th Edition):

Frietze, Kathryn Marie. “Characterization of subspecies B1 human adenovirus ORF E3-10.9K.” 2010. Web. 22 May 2019.

Vancouver:

Frietze KM. Characterization of subspecies B1 human adenovirus ORF E3-10.9K. [Internet] [Doctoral dissertation]. University of New Mexico; 2010. [cited 2019 May 22]. Available from: https://digitalrepository.unm.edu/biom_etds/24.

Council of Science Editors:

Frietze KM. Characterization of subspecies B1 human adenovirus ORF E3-10.9K. [Doctoral Dissertation]. University of New Mexico; 2010. Available from: https://digitalrepository.unm.edu/biom_etds/24


University of New Mexico

12. Ho, Antoine. Next-Generation Sequencing: Acquisition, Analysis, and Assembly.

Degree: Biomedical Sciences Graduate Program, 2013, University of New Mexico

 The process of sequencing a genome involves many steps, and accordingly, this project contains work from each of those steps. Genome sequencing begins with acquisition… (more)

Subjects/Keywords: Sequencing; Next-Generation; Analysis; Assembly; Sequencing By Ligation; Comparison

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ho, A. (2013). Next-Generation Sequencing: Acquisition, Analysis, and Assembly. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/129

Chicago Manual of Style (16th Edition):

Ho, Antoine. “Next-Generation Sequencing: Acquisition, Analysis, and Assembly.” 2013. Doctoral Dissertation, University of New Mexico. Accessed May 22, 2019. https://digitalrepository.unm.edu/biom_etds/129.

MLA Handbook (7th Edition):

Ho, Antoine. “Next-Generation Sequencing: Acquisition, Analysis, and Assembly.” 2013. Web. 22 May 2019.

Vancouver:

Ho A. Next-Generation Sequencing: Acquisition, Analysis, and Assembly. [Internet] [Doctoral dissertation]. University of New Mexico; 2013. [cited 2019 May 22]. Available from: https://digitalrepository.unm.edu/biom_etds/129.

Council of Science Editors:

Ho A. Next-Generation Sequencing: Acquisition, Analysis, and Assembly. [Doctoral Dissertation]. University of New Mexico; 2013. Available from: https://digitalrepository.unm.edu/biom_etds/129


University of New Mexico

13. Brown, Bradley. The RNA binding and RNA chaperone activity of Sin Nombre virus nucleocapsid.

Degree: Biomedical Sciences Graduate Program, 2008, University of New Mexico

 Sin Nombre Virus (SNV) is a member of the hantavirus genus in the Bunyaviridae family. Hantaviruses contain a tripartite negative sense RNA genome with individual… (more)

Subjects/Keywords: Bunyaviridae; Nucleocapsid

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Brown, B. (2008). The RNA binding and RNA chaperone activity of Sin Nombre virus nucleocapsid. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/102

Chicago Manual of Style (16th Edition):

Brown, Bradley. “The RNA binding and RNA chaperone activity of Sin Nombre virus nucleocapsid.” 2008. Doctoral Dissertation, University of New Mexico. Accessed May 22, 2019. https://digitalrepository.unm.edu/biom_etds/102.

MLA Handbook (7th Edition):

Brown, Bradley. “The RNA binding and RNA chaperone activity of Sin Nombre virus nucleocapsid.” 2008. Web. 22 May 2019.

Vancouver:

Brown B. The RNA binding and RNA chaperone activity of Sin Nombre virus nucleocapsid. [Internet] [Doctoral dissertation]. University of New Mexico; 2008. [cited 2019 May 22]. Available from: https://digitalrepository.unm.edu/biom_etds/102.

Council of Science Editors:

Brown B. The RNA binding and RNA chaperone activity of Sin Nombre virus nucleocapsid. [Doctoral Dissertation]. University of New Mexico; 2008. Available from: https://digitalrepository.unm.edu/biom_etds/102

.