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You searched for +publisher:"University of New Mexico" +contributor:("Ozbun, Michelle"). Showing records 1 – 16 of 16 total matches.

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University of New Mexico

1. 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 June 18, 2019. 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. 18 Jun 2019.

Vancouver:

Hunter Z. Induction of mucosal immunity using virus-like particle based vaccines. [Internet] [Doctoral dissertation]. University of New Mexico; 2011. [cited 2019 Jun 18]. 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 New Mexico

2. Dickson, Laura. Molecular dynamics of adenovirus type 3 and 7 infections in military and civilian populations in the United States.

Degree: Biomedical Sciences Graduate Program, 2009, University of New Mexico

 Human adenoviruses (HAdV) are major causative agents of acute respiratory disease (ARD) worldwide. Military recruits and children are two of the populations most susceptible to… (more)

Subjects/Keywords: Adenovirus; Epidemiology

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APA (6th Edition):

Dickson, L. (2009). Molecular dynamics of adenovirus type 3 and 7 infections in military and civilian populations in the United States. (Masters Thesis). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/42

Chicago Manual of Style (16th Edition):

Dickson, Laura. “Molecular dynamics of adenovirus type 3 and 7 infections in military and civilian populations in the United States.” 2009. Masters Thesis, University of New Mexico. Accessed June 18, 2019. https://digitalrepository.unm.edu/biom_etds/42.

MLA Handbook (7th Edition):

Dickson, Laura. “Molecular dynamics of adenovirus type 3 and 7 infections in military and civilian populations in the United States.” 2009. Web. 18 Jun 2019.

Vancouver:

Dickson L. Molecular dynamics of adenovirus type 3 and 7 infections in military and civilian populations in the United States. [Internet] [Masters thesis]. University of New Mexico; 2009. [cited 2019 Jun 18]. Available from: https://digitalrepository.unm.edu/biom_etds/42.

Council of Science Editors:

Dickson L. Molecular dynamics of adenovirus type 3 and 7 infections in military and civilian populations in the United States. [Masters Thesis]. University of New Mexico; 2009. Available from: https://digitalrepository.unm.edu/biom_etds/42


University of New Mexico

3. Flores, Sonya Persia. The role of furin in human papillomavirus infection.

Degree: Biomedical Sciences Graduate Program, 2012, University of New Mexico

 Human papillomaviruses (HPVs) are the causative agent of cervical cancer and infect skin and mucosal membranes. Through wounding the virus establishes infection in the basal… (more)

Subjects/Keywords: HPV; Furin

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APA (6th Edition):

Flores, S. P. (2012). The role of furin in human papillomavirus infection. (Masters Thesis). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/60

Chicago Manual of Style (16th Edition):

Flores, Sonya Persia. “The role of furin in human papillomavirus infection.” 2012. Masters Thesis, University of New Mexico. Accessed June 18, 2019. https://digitalrepository.unm.edu/biom_etds/60.

MLA Handbook (7th Edition):

Flores, Sonya Persia. “The role of furin in human papillomavirus infection.” 2012. Web. 18 Jun 2019.

Vancouver:

Flores SP. The role of furin in human papillomavirus infection. [Internet] [Masters thesis]. University of New Mexico; 2012. [cited 2019 Jun 18]. Available from: https://digitalrepository.unm.edu/biom_etds/60.

Council of Science Editors:

Flores SP. The role of furin in human papillomavirus infection. [Masters Thesis]. University of New Mexico; 2012. Available from: https://digitalrepository.unm.edu/biom_etds/60


University of New Mexico

4. 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

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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 June 18, 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. 18 Jun 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 Jun 18]. 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

5. 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

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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 June 18, 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. 18 Jun 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 Jun 18]. 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

6. 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

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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 June 18, 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. 18 Jun 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 Jun 18]. 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

7. Quan, Krystle K. The Role of Snai2/Slug in Diabetes-impaired Wound Healing.

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

 Impaired wound healing is a common complication of diabetes mellitus. Advanced glycation end products (AGEs) are a consequence of diabetes and are formed from non-enzymatic… (more)

Subjects/Keywords: EGFR; Diabetes; Glyoxal; Snai2; Wound Healing; Advanced Glycation End Products

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APA (6th Edition):

Quan, K. K. (2013). The Role of Snai2/Slug in Diabetes-impaired Wound Healing. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/141

Chicago Manual of Style (16th Edition):

Quan, Krystle K. “The Role of Snai2/Slug in Diabetes-impaired Wound Healing.” 2013. Doctoral Dissertation, University of New Mexico. Accessed June 18, 2019. https://digitalrepository.unm.edu/biom_etds/141.

MLA Handbook (7th Edition):

Quan, Krystle K. “The Role of Snai2/Slug in Diabetes-impaired Wound Healing.” 2013. Web. 18 Jun 2019.

Vancouver:

Quan KK. The Role of Snai2/Slug in Diabetes-impaired Wound Healing. [Internet] [Doctoral dissertation]. University of New Mexico; 2013. [cited 2019 Jun 18]. Available from: https://digitalrepository.unm.edu/biom_etds/141.

Council of Science Editors:

Quan KK. The Role of Snai2/Slug in Diabetes-impaired Wound Healing. [Doctoral Dissertation]. University of New Mexico; 2013. Available from: https://digitalrepository.unm.edu/biom_etds/141


University of New Mexico

8. 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 June 18, 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. 18 Jun 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 Jun 18]. 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

9. 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 June 18, 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. 18 Jun 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 Jun 18]. 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

10. Griego, Anastacia. Evaluation of the Epidermal Growth Factor Receptor Signaling Pathway as a Therapeutic Target in Human Papillomavirus-Associated Disease.

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

  Human papillomaviruses (HPVs) are the most common sexually transmitted infectious agents. They are responsible for >99% of all cervical cancers as well as subsets… (more)

Subjects/Keywords: HPV; EGFR; growth factor receptor; human papillomavirus; cetuximab; cancer; Medicine and Health Sciences

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APA (6th Edition):

Griego, A. (2016). Evaluation of the Epidermal Growth Factor Receptor Signaling Pathway as a Therapeutic Target in Human Papillomavirus-Associated Disease. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/155

Chicago Manual of Style (16th Edition):

Griego, Anastacia. “Evaluation of the Epidermal Growth Factor Receptor Signaling Pathway as a Therapeutic Target in Human Papillomavirus-Associated Disease.” 2016. Doctoral Dissertation, University of New Mexico. Accessed June 18, 2019. https://digitalrepository.unm.edu/biom_etds/155.

MLA Handbook (7th Edition):

Griego, Anastacia. “Evaluation of the Epidermal Growth Factor Receptor Signaling Pathway as a Therapeutic Target in Human Papillomavirus-Associated Disease.” 2016. Web. 18 Jun 2019.

Vancouver:

Griego A. Evaluation of the Epidermal Growth Factor Receptor Signaling Pathway as a Therapeutic Target in Human Papillomavirus-Associated Disease. [Internet] [Doctoral dissertation]. University of New Mexico; 2016. [cited 2019 Jun 18]. Available from: https://digitalrepository.unm.edu/biom_etds/155.

Council of Science Editors:

Griego A. Evaluation of the Epidermal Growth Factor Receptor Signaling Pathway as a Therapeutic Target in Human Papillomavirus-Associated Disease. [Doctoral Dissertation]. University of New Mexico; 2016. Available from: https://digitalrepository.unm.edu/biom_etds/155


University of New Mexico

11. Song, Hebin. Inducible heat shock protein 70 enhances human papillomavirus type 31 genome replication, viral capsid protein nuclear localization and progeny virion morphogenesis in human keratinocytes.

Degree: Biomedical Sciences Graduate Program, 2009, University of New Mexico

 Human papillomaviruses (HPVs) are small, non-enveloped double stranded DNA viruses that demonstrate a strict species and cell type tropism for human epithelial cells. The association… (more)

Subjects/Keywords: human papillomavirus; Heat shock protein; co-factors; chaperone; epithelium; virus morphogenesis; genital infection; cervical cancer

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APA (6th Edition):

Song, H. (2009). Inducible heat shock protein 70 enhances human papillomavirus type 31 genome replication, viral capsid protein nuclear localization and progeny virion morphogenesis in human keratinocytes. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/4

Chicago Manual of Style (16th Edition):

Song, Hebin. “Inducible heat shock protein 70 enhances human papillomavirus type 31 genome replication, viral capsid protein nuclear localization and progeny virion morphogenesis in human keratinocytes.” 2009. Doctoral Dissertation, University of New Mexico. Accessed June 18, 2019. https://digitalrepository.unm.edu/biom_etds/4.

MLA Handbook (7th Edition):

Song, Hebin. “Inducible heat shock protein 70 enhances human papillomavirus type 31 genome replication, viral capsid protein nuclear localization and progeny virion morphogenesis in human keratinocytes.” 2009. Web. 18 Jun 2019.

Vancouver:

Song H. Inducible heat shock protein 70 enhances human papillomavirus type 31 genome replication, viral capsid protein nuclear localization and progeny virion morphogenesis in human keratinocytes. [Internet] [Doctoral dissertation]. University of New Mexico; 2009. [cited 2019 Jun 18]. Available from: https://digitalrepository.unm.edu/biom_etds/4.

Council of Science Editors:

Song H. Inducible heat shock protein 70 enhances human papillomavirus type 31 genome replication, viral capsid protein nuclear localization and progeny virion morphogenesis in human keratinocytes. [Doctoral Dissertation]. University of New Mexico; 2009. Available from: https://digitalrepository.unm.edu/biom_etds/4


University of New Mexico

12. 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

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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 June 18, 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. 18 Jun 2019.

Vancouver:

Frietze KM. Characterization of subspecies B1 human adenovirus ORF E3-10.9K. [Internet] [Doctoral dissertation]. University of New Mexico; 2010. [cited 2019 Jun 18]. 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

13. Sully, Erin. Small molecule inhibition of Staphylococcus aureus virulence.

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

 The increasing emergence of antibiotic resistant Staphylococcus aureus infections, particularly those caused by a single clone of methicillin resistant S. aureus (USA300 MRSA), coupled with… (more)

Subjects/Keywords: CA-MRSA; staphylococcus aureus; small molecule inhibitor; high-throughput screen; virulence; quorum sensing

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APA (6th Edition):

Sully, E. (2011). Small molecule inhibition of Staphylococcus aureus virulence. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/39

Chicago Manual of Style (16th Edition):

Sully, Erin. “Small molecule inhibition of Staphylococcus aureus virulence.” 2011. Doctoral Dissertation, University of New Mexico. Accessed June 18, 2019. https://digitalrepository.unm.edu/biom_etds/39.

MLA Handbook (7th Edition):

Sully, Erin. “Small molecule inhibition of Staphylococcus aureus virulence.” 2011. Web. 18 Jun 2019.

Vancouver:

Sully E. Small molecule inhibition of Staphylococcus aureus virulence. [Internet] [Doctoral dissertation]. University of New Mexico; 2011. [cited 2019 Jun 18]. Available from: https://digitalrepository.unm.edu/biom_etds/39.

Council of Science Editors:

Sully E. Small molecule inhibition of Staphylococcus aureus virulence. [Doctoral Dissertation]. University of New Mexico; 2011. Available from: https://digitalrepository.unm.edu/biom_etds/39


University of New Mexico

14. Plourde, Jennifer. Neuropathogenesis of highly pathogenic avian influenza in ferrets following intranasal instillation or aerosol exposure to low doses.

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

 Highly pathogenic avian influenza (HPAI), subtype H5N1, has continued to infect humans every year since its initial outbreak in 1997. The overall mortality is approximately… (more)

Subjects/Keywords: highly pathogenic avian influenza; H5N1; ferrets; neurovirulence; pathogenesis; aerosol model

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APA (6th Edition):

Plourde, J. (2013). Neuropathogenesis of highly pathogenic avian influenza in ferrets following intranasal instillation or aerosol exposure to low doses. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/139

Chicago Manual of Style (16th Edition):

Plourde, Jennifer. “Neuropathogenesis of highly pathogenic avian influenza in ferrets following intranasal instillation or aerosol exposure to low doses.” 2013. Doctoral Dissertation, University of New Mexico. Accessed June 18, 2019. https://digitalrepository.unm.edu/biom_etds/139.

MLA Handbook (7th Edition):

Plourde, Jennifer. “Neuropathogenesis of highly pathogenic avian influenza in ferrets following intranasal instillation or aerosol exposure to low doses.” 2013. Web. 18 Jun 2019.

Vancouver:

Plourde J. Neuropathogenesis of highly pathogenic avian influenza in ferrets following intranasal instillation or aerosol exposure to low doses. [Internet] [Doctoral dissertation]. University of New Mexico; 2013. [cited 2019 Jun 18]. Available from: https://digitalrepository.unm.edu/biom_etds/139.

Council of Science Editors:

Plourde J. Neuropathogenesis of highly pathogenic avian influenza in ferrets following intranasal instillation or aerosol exposure to low doses. [Doctoral Dissertation]. University of New Mexico; 2013. Available from: https://digitalrepository.unm.edu/biom_etds/139


University of New Mexico

15. Vaughan, Sarah. THE IMMUNOLOGICAL MECHANISMS OF INFLUENZA VACCINATION: A COMPARISON BETWEEN A SEASONAL SUBUNIT VACCINE AND AN H5N1 SUBUNIT VACCINE WITH AND WITHOUT ALUM ADJUVANT.

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

 Highly pathogenic avian influenza (HPAI) H5N1 is an emerging infectious virus with a 60% fatality rate in humans. In the United States, a vaccine for… (more)

Subjects/Keywords: Influenza; Highly Pathogenic Avian Influenza; H5N1; Influenza Vaccine; Immune Response to Vaccination; C-type Lectin Receptors; BALB/c Mice; Bone Marrow Derived Dendritic Cells; Adjuvant; Alum; H5N1 Vaccine

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APA (6th Edition):

Vaughan, S. (2013). THE IMMUNOLOGICAL MECHANISMS OF INFLUENZA VACCINATION: A COMPARISON BETWEEN A SEASONAL SUBUNIT VACCINE AND AN H5N1 SUBUNIT VACCINE WITH AND WITHOUT ALUM ADJUVANT. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/148

Chicago Manual of Style (16th Edition):

Vaughan, Sarah. “THE IMMUNOLOGICAL MECHANISMS OF INFLUENZA VACCINATION: A COMPARISON BETWEEN A SEASONAL SUBUNIT VACCINE AND AN H5N1 SUBUNIT VACCINE WITH AND WITHOUT ALUM ADJUVANT.” 2013. Doctoral Dissertation, University of New Mexico. Accessed June 18, 2019. https://digitalrepository.unm.edu/biom_etds/148.

MLA Handbook (7th Edition):

Vaughan, Sarah. “THE IMMUNOLOGICAL MECHANISMS OF INFLUENZA VACCINATION: A COMPARISON BETWEEN A SEASONAL SUBUNIT VACCINE AND AN H5N1 SUBUNIT VACCINE WITH AND WITHOUT ALUM ADJUVANT.” 2013. Web. 18 Jun 2019.

Vancouver:

Vaughan S. THE IMMUNOLOGICAL MECHANISMS OF INFLUENZA VACCINATION: A COMPARISON BETWEEN A SEASONAL SUBUNIT VACCINE AND AN H5N1 SUBUNIT VACCINE WITH AND WITHOUT ALUM ADJUVANT. [Internet] [Doctoral dissertation]. University of New Mexico; 2013. [cited 2019 Jun 18]. Available from: https://digitalrepository.unm.edu/biom_etds/148.

Council of Science Editors:

Vaughan S. THE IMMUNOLOGICAL MECHANISMS OF INFLUENZA VACCINATION: A COMPARISON BETWEEN A SEASONAL SUBUNIT VACCINE AND AN H5N1 SUBUNIT VACCINE WITH AND WITHOUT ALUM ADJUVANT. [Doctoral Dissertation]. University of New Mexico; 2013. Available from: https://digitalrepository.unm.edu/biom_etds/148


University of New Mexico

16. Smith, Jessica. Entry and trafficking of human papillomavirus type 31 into human keratinocytes.

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

 Human papillomaviruses (HPVs) are small, nonenveloped double stranded DNA viruses that display a strict species and cell type tropism for human epithelial cells. The association… (more)

Subjects/Keywords: papillomavirus; virus entry; caveolae; rab gtpase; filopodia

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APA (6th Edition):

Smith, J. (2008). Entry and trafficking of human papillomavirus type 31 into human keratinocytes. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/103

Chicago Manual of Style (16th Edition):

Smith, Jessica. “Entry and trafficking of human papillomavirus type 31 into human keratinocytes.” 2008. Doctoral Dissertation, University of New Mexico. Accessed June 18, 2019. https://digitalrepository.unm.edu/biom_etds/103.

MLA Handbook (7th Edition):

Smith, Jessica. “Entry and trafficking of human papillomavirus type 31 into human keratinocytes.” 2008. Web. 18 Jun 2019.

Vancouver:

Smith J. Entry and trafficking of human papillomavirus type 31 into human keratinocytes. [Internet] [Doctoral dissertation]. University of New Mexico; 2008. [cited 2019 Jun 18]. Available from: https://digitalrepository.unm.edu/biom_etds/103.

Council of Science Editors:

Smith J. Entry and trafficking of human papillomavirus type 31 into human keratinocytes. [Doctoral Dissertation]. University of New Mexico; 2008. Available from: https://digitalrepository.unm.edu/biom_etds/103

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