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You searched for subject:(SIV). Showing records 1 – 30 of 107 total matches.

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Tulane University

1. Bucsan, Allison. CD4-Independent Correlates of Protection in M. tuberculosis and Mtb/SIV Co-Infection.

Degree: 2018, Tulane University

[email protected]

In order to develop better therapeutics and treatment strategies for tuberculosis (TB) infection, it is imperative to understand interactions that occur in the host… (more)

Subjects/Keywords: SIV

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APA (6th Edition):

Bucsan, A. (2018). CD4-Independent Correlates of Protection in M. tuberculosis and Mtb/SIV Co-Infection. (Thesis). Tulane University. Retrieved from https://digitallibrary.tulane.edu/islandora/object/tulane:87914

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):

Bucsan, Allison. “CD4-Independent Correlates of Protection in M. tuberculosis and Mtb/SIV Co-Infection.” 2018. Thesis, Tulane University. Accessed September 26, 2020. https://digitallibrary.tulane.edu/islandora/object/tulane:87914.

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

MLA Handbook (7th Edition):

Bucsan, Allison. “CD4-Independent Correlates of Protection in M. tuberculosis and Mtb/SIV Co-Infection.” 2018. Web. 26 Sep 2020.

Vancouver:

Bucsan A. CD4-Independent Correlates of Protection in M. tuberculosis and Mtb/SIV Co-Infection. [Internet] [Thesis]. Tulane University; 2018. [cited 2020 Sep 26]. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:87914.

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

Council of Science Editors:

Bucsan A. CD4-Independent Correlates of Protection in M. tuberculosis and Mtb/SIV Co-Infection. [Thesis]. Tulane University; 2018. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:87914

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

2. Beck, Sarah Evelyn. IMMUNE SELECTION IN THE CNS: CONSEQUENCES OF SIV GAG ESCAPE FROM MHC CLASS I-MEDIATED CONTROL.

Degree: 2014, Johns Hopkins University

 Immune pressure exerted by host factors including MHC class I-mediated cytotoxic T cell control affects HIV disease progression and drives the development of viral escape… (more)

Subjects/Keywords: SIV; MHC class I; encephalitis

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APA (6th Edition):

Beck, S. E. (2014). IMMUNE SELECTION IN THE CNS: CONSEQUENCES OF SIV GAG ESCAPE FROM MHC CLASS I-MEDIATED CONTROL. (Thesis). Johns Hopkins University. Retrieved from http://jhir.library.jhu.edu/handle/1774.2/36978

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):

Beck, Sarah Evelyn. “IMMUNE SELECTION IN THE CNS: CONSEQUENCES OF SIV GAG ESCAPE FROM MHC CLASS I-MEDIATED CONTROL.” 2014. Thesis, Johns Hopkins University. Accessed September 26, 2020. http://jhir.library.jhu.edu/handle/1774.2/36978.

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

MLA Handbook (7th Edition):

Beck, Sarah Evelyn. “IMMUNE SELECTION IN THE CNS: CONSEQUENCES OF SIV GAG ESCAPE FROM MHC CLASS I-MEDIATED CONTROL.” 2014. Web. 26 Sep 2020.

Vancouver:

Beck SE. IMMUNE SELECTION IN THE CNS: CONSEQUENCES OF SIV GAG ESCAPE FROM MHC CLASS I-MEDIATED CONTROL. [Internet] [Thesis]. Johns Hopkins University; 2014. [cited 2020 Sep 26]. Available from: http://jhir.library.jhu.edu/handle/1774.2/36978.

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

Council of Science Editors:

Beck SE. IMMUNE SELECTION IN THE CNS: CONSEQUENCES OF SIV GAG ESCAPE FROM MHC CLASS I-MEDIATED CONTROL. [Thesis]. Johns Hopkins University; 2014. Available from: http://jhir.library.jhu.edu/handle/1774.2/36978

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


University of Pennsylvania

3. Elser, Samra Elisabeth. The Role of the Gp41 Membrane-Proximal Tyrosine Motif in Simian Immunodeficiency Virus Pathogenesis.

Degree: 2016, University of Pennsylvania

 A tyrosine-dependent sorting signal in membrane-proximal region of the envelope protein cytoplasmic tail domain is conserved across all primate lentiviruses. It is known to be… (more)

Subjects/Keywords: HIV; pathogenesis; SIV; virology; Virology

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APA (6th Edition):

Elser, S. E. (2016). The Role of the Gp41 Membrane-Proximal Tyrosine Motif in Simian Immunodeficiency Virus Pathogenesis. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1699

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):

Elser, Samra Elisabeth. “The Role of the Gp41 Membrane-Proximal Tyrosine Motif in Simian Immunodeficiency Virus Pathogenesis.” 2016. Thesis, University of Pennsylvania. Accessed September 26, 2020. https://repository.upenn.edu/edissertations/1699.

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

MLA Handbook (7th Edition):

Elser, Samra Elisabeth. “The Role of the Gp41 Membrane-Proximal Tyrosine Motif in Simian Immunodeficiency Virus Pathogenesis.” 2016. Web. 26 Sep 2020.

Vancouver:

Elser SE. The Role of the Gp41 Membrane-Proximal Tyrosine Motif in Simian Immunodeficiency Virus Pathogenesis. [Internet] [Thesis]. University of Pennsylvania; 2016. [cited 2020 Sep 26]. Available from: https://repository.upenn.edu/edissertations/1699.

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

Council of Science Editors:

Elser SE. The Role of the Gp41 Membrane-Proximal Tyrosine Motif in Simian Immunodeficiency Virus Pathogenesis. [Thesis]. University of Pennsylvania; 2016. Available from: https://repository.upenn.edu/edissertations/1699

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


Boston College

4. Lee, Arleide. Investigating the expression and role of proliferating cell nuclear antigen in monocytes and macrophages of SIV infected rhesus macaques.

Degree: MS, Biology, 2010, Boston College

 Proliferating cell nuclear antigen (PCNA) is a DNA polymerase δ auxiliary protein during cell cycle. However, PCNA is also present in quiescent cells undergoing DNA… (more)

Subjects/Keywords: Macrophages; Monocytes; PCNA; SIV

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APA (6th Edition):

Lee, A. (2010). Investigating the expression and role of proliferating cell nuclear antigen in monocytes and macrophages of SIV infected rhesus macaques. (Masters Thesis). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:104466

Chicago Manual of Style (16th Edition):

Lee, Arleide. “Investigating the expression and role of proliferating cell nuclear antigen in monocytes and macrophages of SIV infected rhesus macaques.” 2010. Masters Thesis, Boston College. Accessed September 26, 2020. http://dlib.bc.edu/islandora/object/bc-ir:104466.

MLA Handbook (7th Edition):

Lee, Arleide. “Investigating the expression and role of proliferating cell nuclear antigen in monocytes and macrophages of SIV infected rhesus macaques.” 2010. Web. 26 Sep 2020.

Vancouver:

Lee A. Investigating the expression and role of proliferating cell nuclear antigen in monocytes and macrophages of SIV infected rhesus macaques. [Internet] [Masters thesis]. Boston College; 2010. [cited 2020 Sep 26]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104466.

Council of Science Editors:

Lee A. Investigating the expression and role of proliferating cell nuclear antigen in monocytes and macrophages of SIV infected rhesus macaques. [Masters Thesis]. Boston College; 2010. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104466


Boston College

5. Walker, Joshua Aaron. The Role of Monocytes and Macrophages Pathogenesis of HIV and SIV-Associated Cardiovascular Disease.

Degree: PhD, Biology, 2016, Boston College

 HIV associated cardiovascular disease is likely due to multiple factors ranging from accelerated aging, the direct effects of HIV proteins, and increased inflammation and immune… (more)

Subjects/Keywords: Cardiovascular; HIV; Inflammation; Macrophage; SIV

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APA (6th Edition):

Walker, J. A. (2016). The Role of Monocytes and Macrophages Pathogenesis of HIV and SIV-Associated Cardiovascular Disease. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:107030

Chicago Manual of Style (16th Edition):

Walker, Joshua Aaron. “The Role of Monocytes and Macrophages Pathogenesis of HIV and SIV-Associated Cardiovascular Disease.” 2016. Doctoral Dissertation, Boston College. Accessed September 26, 2020. http://dlib.bc.edu/islandora/object/bc-ir:107030.

MLA Handbook (7th Edition):

Walker, Joshua Aaron. “The Role of Monocytes and Macrophages Pathogenesis of HIV and SIV-Associated Cardiovascular Disease.” 2016. Web. 26 Sep 2020.

Vancouver:

Walker JA. The Role of Monocytes and Macrophages Pathogenesis of HIV and SIV-Associated Cardiovascular Disease. [Internet] [Doctoral dissertation]. Boston College; 2016. [cited 2020 Sep 26]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107030.

Council of Science Editors:

Walker JA. The Role of Monocytes and Macrophages Pathogenesis of HIV and SIV-Associated Cardiovascular Disease. [Doctoral Dissertation]. Boston College; 2016. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107030


Tulane University

6. Fahlberg, Marissa D. The Impact of Simian Immunodeficiency Virus on Subcutaneous Adipose Tissue of Rhesus Macaques.

Degree: 2018, Tulane University

[email protected]

Background: Individuals with human immunodeficiency virus (HIV) and undergoing antiretroviral therapy (ART) exhibit high levels of circulating inflammatory cytokines and proteins, which are strongly… (more)

Subjects/Keywords: SIV; Rhesus Macaques; Adipose tissue

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APA (6th Edition):

Fahlberg, M. D. (2018). The Impact of Simian Immunodeficiency Virus on Subcutaneous Adipose Tissue of Rhesus Macaques. (Thesis). Tulane University. Retrieved from https://digitallibrary.tulane.edu/islandora/object/tulane:110475

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):

Fahlberg, Marissa D. “The Impact of Simian Immunodeficiency Virus on Subcutaneous Adipose Tissue of Rhesus Macaques.” 2018. Thesis, Tulane University. Accessed September 26, 2020. https://digitallibrary.tulane.edu/islandora/object/tulane:110475.

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

MLA Handbook (7th Edition):

Fahlberg, Marissa D. “The Impact of Simian Immunodeficiency Virus on Subcutaneous Adipose Tissue of Rhesus Macaques.” 2018. Web. 26 Sep 2020.

Vancouver:

Fahlberg MD. The Impact of Simian Immunodeficiency Virus on Subcutaneous Adipose Tissue of Rhesus Macaques. [Internet] [Thesis]. Tulane University; 2018. [cited 2020 Sep 26]. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:110475.

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

Council of Science Editors:

Fahlberg MD. The Impact of Simian Immunodeficiency Virus on Subcutaneous Adipose Tissue of Rhesus Macaques. [Thesis]. Tulane University; 2018. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:110475

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


University of Miami

7. Rainho, Jennifer Nina. Examining The Role of Nef in the Resistance of SIV–Infected Macrophages to CD8+ T Cell Suppression.

Degree: PhD, Microbiology and Immunology (Medicine), 2015, University of Miami

  SIV–specific CD8+ T cells kill SIV–infected CD4+ T cells in an MHC Class I (MHC–I) dependent manner. However, they are reportedly less efficient at… (more)

Subjects/Keywords: macrophages; SIV; CD8; Suppression

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APA (6th Edition):

Rainho, J. N. (2015). Examining The Role of Nef in the Resistance of SIV–Infected Macrophages to CD8+ T Cell Suppression. (Doctoral Dissertation). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_dissertations/1517

Chicago Manual of Style (16th Edition):

Rainho, Jennifer Nina. “Examining The Role of Nef in the Resistance of SIV–Infected Macrophages to CD8+ T Cell Suppression.” 2015. Doctoral Dissertation, University of Miami. Accessed September 26, 2020. https://scholarlyrepository.miami.edu/oa_dissertations/1517.

MLA Handbook (7th Edition):

Rainho, Jennifer Nina. “Examining The Role of Nef in the Resistance of SIV–Infected Macrophages to CD8+ T Cell Suppression.” 2015. Web. 26 Sep 2020.

Vancouver:

Rainho JN. Examining The Role of Nef in the Resistance of SIV–Infected Macrophages to CD8+ T Cell Suppression. [Internet] [Doctoral dissertation]. University of Miami; 2015. [cited 2020 Sep 26]. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/1517.

Council of Science Editors:

Rainho JN. Examining The Role of Nef in the Resistance of SIV–Infected Macrophages to CD8+ T Cell Suppression. [Doctoral Dissertation]. University of Miami; 2015. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/1517


University of Melbourne

8. GOONERATNE, DONA. The role of Major Histocompatibility Complex class I in Human Immunodeficiency Virus-1 and Simian Immunodeficiency Virus infections.

Degree: 2016, University of Melbourne

 The first official report of AIDS was in 1981. Since then, the HIV-1 infection has reached a pandemic state and high rates of infection are… (more)

Subjects/Keywords: MHC I; HIV-1; SIV

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APA (6th Edition):

GOONERATNE, D. (2016). The role of Major Histocompatibility Complex class I in Human Immunodeficiency Virus-1 and Simian Immunodeficiency Virus infections. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/108677

Chicago Manual of Style (16th Edition):

GOONERATNE, DONA. “The role of Major Histocompatibility Complex class I in Human Immunodeficiency Virus-1 and Simian Immunodeficiency Virus infections.” 2016. Doctoral Dissertation, University of Melbourne. Accessed September 26, 2020. http://hdl.handle.net/11343/108677.

MLA Handbook (7th Edition):

GOONERATNE, DONA. “The role of Major Histocompatibility Complex class I in Human Immunodeficiency Virus-1 and Simian Immunodeficiency Virus infections.” 2016. Web. 26 Sep 2020.

Vancouver:

GOONERATNE D. The role of Major Histocompatibility Complex class I in Human Immunodeficiency Virus-1 and Simian Immunodeficiency Virus infections. [Internet] [Doctoral dissertation]. University of Melbourne; 2016. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/11343/108677.

Council of Science Editors:

GOONERATNE D. The role of Major Histocompatibility Complex class I in Human Immunodeficiency Virus-1 and Simian Immunodeficiency Virus infections. [Doctoral Dissertation]. University of Melbourne; 2016. Available from: http://hdl.handle.net/11343/108677

9. García Téllez, Thalia Alejandra. Study of inflammasome activation in monocytes, macrophages and epithelial cells during SIV infection in a pathogenic and a non-pathogenic model : Etude de l’activation de l’inflammasome dans les monocytes, macrophages et cellules épithéliales lors de l’infection SIV dans des modelés pathogène et non-pathogène.

Degree: Docteur es, Sciences de la vie et de la santé. Infectiologie, 2018, Sorbonne Paris Cité

Chez les individus infectés par le VIH on observe une augmentation de l’inflammation et de l’activation immunitaire (AI) qui est associée à la progression vers… (more)

Subjects/Keywords: SIV; Barrière épithéliale; Hôtes naturels; SIV; Epithelial barrier; Natural hosts

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APA (6th Edition):

García Téllez, T. A. (2018). Study of inflammasome activation in monocytes, macrophages and epithelial cells during SIV infection in a pathogenic and a non-pathogenic model : Etude de l’activation de l’inflammasome dans les monocytes, macrophages et cellules épithéliales lors de l’infection SIV dans des modelés pathogène et non-pathogène. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2018USPCC300

Chicago Manual of Style (16th Edition):

García Téllez, Thalia Alejandra. “Study of inflammasome activation in monocytes, macrophages and epithelial cells during SIV infection in a pathogenic and a non-pathogenic model : Etude de l’activation de l’inflammasome dans les monocytes, macrophages et cellules épithéliales lors de l’infection SIV dans des modelés pathogène et non-pathogène.” 2018. Doctoral Dissertation, Sorbonne Paris Cité. Accessed September 26, 2020. http://www.theses.fr/2018USPCC300.

MLA Handbook (7th Edition):

García Téllez, Thalia Alejandra. “Study of inflammasome activation in monocytes, macrophages and epithelial cells during SIV infection in a pathogenic and a non-pathogenic model : Etude de l’activation de l’inflammasome dans les monocytes, macrophages et cellules épithéliales lors de l’infection SIV dans des modelés pathogène et non-pathogène.” 2018. Web. 26 Sep 2020.

Vancouver:

García Téllez TA. Study of inflammasome activation in monocytes, macrophages and epithelial cells during SIV infection in a pathogenic and a non-pathogenic model : Etude de l’activation de l’inflammasome dans les monocytes, macrophages et cellules épithéliales lors de l’infection SIV dans des modelés pathogène et non-pathogène. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2018. [cited 2020 Sep 26]. Available from: http://www.theses.fr/2018USPCC300.

Council of Science Editors:

García Téllez TA. Study of inflammasome activation in monocytes, macrophages and epithelial cells during SIV infection in a pathogenic and a non-pathogenic model : Etude de l’activation de l’inflammasome dans les monocytes, macrophages et cellules épithéliales lors de l’infection SIV dans des modelés pathogène et non-pathogène. [Doctoral Dissertation]. Sorbonne Paris Cité; 2018. Available from: http://www.theses.fr/2018USPCC300


University of California – Berkeley

10. Baker, Christopher Arthur Renfrew. The Impact of Fetal Exposure to SIV on the Outcome of Neonatal Infection.

Degree: Infectious Diseases & Immunity, 2013, University of California – Berkeley

 HIV kills more than 2 million people worldwide, annually. Progressive HIV disease is marked by the loss of peripheral CD4+ T cells, leading to immune… (more)

Subjects/Keywords: Immunology; Public health; macaque; microchimerism; SIV; tolerance

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APA (6th Edition):

Baker, C. A. R. (2013). The Impact of Fetal Exposure to SIV on the Outcome of Neonatal Infection. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/4pf7p02v

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):

Baker, Christopher Arthur Renfrew. “The Impact of Fetal Exposure to SIV on the Outcome of Neonatal Infection.” 2013. Thesis, University of California – Berkeley. Accessed September 26, 2020. http://www.escholarship.org/uc/item/4pf7p02v.

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

MLA Handbook (7th Edition):

Baker, Christopher Arthur Renfrew. “The Impact of Fetal Exposure to SIV on the Outcome of Neonatal Infection.” 2013. Web. 26 Sep 2020.

Vancouver:

Baker CAR. The Impact of Fetal Exposure to SIV on the Outcome of Neonatal Infection. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2020 Sep 26]. Available from: http://www.escholarship.org/uc/item/4pf7p02v.

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

Council of Science Editors:

Baker CAR. The Impact of Fetal Exposure to SIV on the Outcome of Neonatal Infection. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/4pf7p02v

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


University of Manchester

11. Faqih, Layla Ahmed A. HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems.

Degree: 2018, University of Manchester

 Production of an effective vaccine and long-term treatment against human immunodeficiency virus (HIV) is elusive. In this thesis two different techniques were used in an… (more)

Subjects/Keywords: HIV; SIV; Genetherapy; Immunotherapy; Vaccination; Baculovirus; BacMam

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APA (6th Edition):

Faqih, L. A. A. (2018). HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:315559

Chicago Manual of Style (16th Edition):

Faqih, Layla Ahmed A. “HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems.” 2018. Doctoral Dissertation, University of Manchester. Accessed September 26, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:315559.

MLA Handbook (7th Edition):

Faqih, Layla Ahmed A. “HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems.” 2018. Web. 26 Sep 2020.

Vancouver:

Faqih LAA. HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2020 Sep 26]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:315559.

Council of Science Editors:

Faqih LAA. HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems. [Doctoral Dissertation]. University of Manchester; 2018. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:315559


University of Miami

12. Plitnik, Timothy Edward. Reverse Transcriptase and the Inability of SAMHD1 to Fully Restrict Macrophage Infection by HIV-1.

Degree: PhD, Microbiology and Immunology (Medicine), 2019, University of Miami

 HIV/AIDS continues to cause significant morbidity and mortality across the globe. Even though current drug therapy can reduce the disease burden, a cure to HIV-1… (more)

Subjects/Keywords: HIV-1; SIV; SAMHD1; Vpx; Macrophage; SHIV

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APA (6th Edition):

Plitnik, T. E. (2019). Reverse Transcriptase and the Inability of SAMHD1 to Fully Restrict Macrophage Infection by HIV-1. (Doctoral Dissertation). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_dissertations/2259

Chicago Manual of Style (16th Edition):

Plitnik, Timothy Edward. “Reverse Transcriptase and the Inability of SAMHD1 to Fully Restrict Macrophage Infection by HIV-1.” 2019. Doctoral Dissertation, University of Miami. Accessed September 26, 2020. https://scholarlyrepository.miami.edu/oa_dissertations/2259.

MLA Handbook (7th Edition):

Plitnik, Timothy Edward. “Reverse Transcriptase and the Inability of SAMHD1 to Fully Restrict Macrophage Infection by HIV-1.” 2019. Web. 26 Sep 2020.

Vancouver:

Plitnik TE. Reverse Transcriptase and the Inability of SAMHD1 to Fully Restrict Macrophage Infection by HIV-1. [Internet] [Doctoral dissertation]. University of Miami; 2019. [cited 2020 Sep 26]. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/2259.

Council of Science Editors:

Plitnik TE. Reverse Transcriptase and the Inability of SAMHD1 to Fully Restrict Macrophage Infection by HIV-1. [Doctoral Dissertation]. University of Miami; 2019. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/2259


Boston University

13. Pastores, Kevin Clyde Gasmena. Development of novel SHIVs from HIV-1 clades for preclinical evaluation.

Degree: MS, Medical Sciences, 2017, Boston University

 The lack of an animal model that recapitulates the prominent features of HIV-1 infection in humans limits the search for preventative and curative strategies against… (more)

Subjects/Keywords: Virology; HIV-1; Rhesus; SHIV; SIV

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APA (6th Edition):

Pastores, K. C. G. (2017). Development of novel SHIVs from HIV-1 clades for preclinical evaluation. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/23734

Chicago Manual of Style (16th Edition):

Pastores, Kevin Clyde Gasmena. “Development of novel SHIVs from HIV-1 clades for preclinical evaluation.” 2017. Masters Thesis, Boston University. Accessed September 26, 2020. http://hdl.handle.net/2144/23734.

MLA Handbook (7th Edition):

Pastores, Kevin Clyde Gasmena. “Development of novel SHIVs from HIV-1 clades for preclinical evaluation.” 2017. Web. 26 Sep 2020.

Vancouver:

Pastores KCG. Development of novel SHIVs from HIV-1 clades for preclinical evaluation. [Internet] [Masters thesis]. Boston University; 2017. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/2144/23734.

Council of Science Editors:

Pastores KCG. Development of novel SHIVs from HIV-1 clades for preclinical evaluation. [Masters Thesis]. Boston University; 2017. Available from: http://hdl.handle.net/2144/23734

14. Faqih, Layla. HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems.

Degree: PhD, 2018, University of Manchester

 Production of an effective vaccine and long-term treatment against human immunodeficiency virus (HIV) is elusive. In this thesis two different techniques were used in an… (more)

Subjects/Keywords: Vaccination; Baculovirus; BacMam; Genetherapy; SIV; HIV; Immunotherapy

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

APA (6th Edition):

Faqih, L. (2018). HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/hiv-neutralising-antibody-delivered-by-gene-therapy-with-a-hybrid-vacciniaretrovirus-or-bacmamretrovirus-expression-systems(b540de64-0484-461c-9ccf-a59ae3681f7f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.756895

Chicago Manual of Style (16th Edition):

Faqih, Layla. “HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems.” 2018. Doctoral Dissertation, University of Manchester. Accessed September 26, 2020. https://www.research.manchester.ac.uk/portal/en/theses/hiv-neutralising-antibody-delivered-by-gene-therapy-with-a-hybrid-vacciniaretrovirus-or-bacmamretrovirus-expression-systems(b540de64-0484-461c-9ccf-a59ae3681f7f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.756895.

MLA Handbook (7th Edition):

Faqih, Layla. “HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems.” 2018. Web. 26 Sep 2020.

Vancouver:

Faqih L. HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2020 Sep 26]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/hiv-neutralising-antibody-delivered-by-gene-therapy-with-a-hybrid-vacciniaretrovirus-or-bacmamretrovirus-expression-systems(b540de64-0484-461c-9ccf-a59ae3681f7f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.756895.

Council of Science Editors:

Faqih L. HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems. [Doctoral Dissertation]. University of Manchester; 2018. Available from: https://www.research.manchester.ac.uk/portal/en/theses/hiv-neutralising-antibody-delivered-by-gene-therapy-with-a-hybrid-vacciniaretrovirus-or-bacmamretrovirus-expression-systems(b540de64-0484-461c-9ccf-a59ae3681f7f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.756895


University of Manitoba

15. Toledo, Nikki. Cervicovaginal inflammatory cytokine and chemokine responses to two different SIV vaccines in female mauritian cynomolgus macaques.

Degree: Medical Microbiology and Infectious Diseases, 2019, University of Manitoba

 Human immunodeficiency virus (HIV) -1 infects CD4+ T lymphocytes and activated CD4+ T cells are preferentially targeted. This posed great challenges in developing an effective… (more)

Subjects/Keywords: HIV; Mucosal Inflammation; SIV; Vaccine; NHP

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APA (6th Edition):

Toledo, N. (2019). Cervicovaginal inflammatory cytokine and chemokine responses to two different SIV vaccines in female mauritian cynomolgus macaques. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/34172

Chicago Manual of Style (16th Edition):

Toledo, Nikki. “Cervicovaginal inflammatory cytokine and chemokine responses to two different SIV vaccines in female mauritian cynomolgus macaques.” 2019. Masters Thesis, University of Manitoba. Accessed September 26, 2020. http://hdl.handle.net/1993/34172.

MLA Handbook (7th Edition):

Toledo, Nikki. “Cervicovaginal inflammatory cytokine and chemokine responses to two different SIV vaccines in female mauritian cynomolgus macaques.” 2019. Web. 26 Sep 2020.

Vancouver:

Toledo N. Cervicovaginal inflammatory cytokine and chemokine responses to two different SIV vaccines in female mauritian cynomolgus macaques. [Internet] [Masters thesis]. University of Manitoba; 2019. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/1993/34172.

Council of Science Editors:

Toledo N. Cervicovaginal inflammatory cytokine and chemokine responses to two different SIV vaccines in female mauritian cynomolgus macaques. [Masters Thesis]. University of Manitoba; 2019. Available from: http://hdl.handle.net/1993/34172


University of Washington

16. Dross, Sandra. The Kinetics of Myeloid Derived Suppressor Cell Frequency and Function in Chronic Retroviral Infections.

Degree: PhD, 2016, University of Washington

 During chronic retroviral infection, poor clinical outcomes correlate both with systemic inflammation and poor proliferative ability of HIV-specific T cells, however the connection between the… (more)

Subjects/Keywords: HIV; MDSC; SIV; Immunology; Virology; Aging; pathobiology

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

APA (6th Edition):

Dross, S. (2016). The Kinetics of Myeloid Derived Suppressor Cell Frequency and Function in Chronic Retroviral Infections. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/36801

Chicago Manual of Style (16th Edition):

Dross, Sandra. “The Kinetics of Myeloid Derived Suppressor Cell Frequency and Function in Chronic Retroviral Infections.” 2016. Doctoral Dissertation, University of Washington. Accessed September 26, 2020. http://hdl.handle.net/1773/36801.

MLA Handbook (7th Edition):

Dross, Sandra. “The Kinetics of Myeloid Derived Suppressor Cell Frequency and Function in Chronic Retroviral Infections.” 2016. Web. 26 Sep 2020.

Vancouver:

Dross S. The Kinetics of Myeloid Derived Suppressor Cell Frequency and Function in Chronic Retroviral Infections. [Internet] [Doctoral dissertation]. University of Washington; 2016. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/1773/36801.

Council of Science Editors:

Dross S. The Kinetics of Myeloid Derived Suppressor Cell Frequency and Function in Chronic Retroviral Infections. [Doctoral Dissertation]. University of Washington; 2016. Available from: http://hdl.handle.net/1773/36801

17. D'Arc Ferreira da Costa, Mirela. Analyse des aspects génétiques des lentivirus et de leurs hôtes par l’étude non invasive des primates non humains : Analysis of genetic aspects of lentivirus and their hosts with non invasive techniques of non humans primates.

Degree: Docteur es, Biologie Santé, 2015, Montpellier

 Les Virus de l'Immunodéficience Humaine (VIH) sont le résultat de plusieurs transmissions inter-espèces de SIV (Virus de l'Immunodéficience Simienne) de Primates Non Humains (PNH) à… (more)

Subjects/Keywords: Siv; Intégrine; Vih; Non pathogène; Pathogène; Primates; Siv; Integrin; Hiv; Non Pathogenic; Pathogenic; Primates

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APA (6th Edition):

D'Arc Ferreira da Costa, M. (2015). Analyse des aspects génétiques des lentivirus et de leurs hôtes par l’étude non invasive des primates non humains : Analysis of genetic aspects of lentivirus and their hosts with non invasive techniques of non humans primates. (Doctoral Dissertation). Montpellier. Retrieved from http://www.theses.fr/2015MONTT018

Chicago Manual of Style (16th Edition):

D'Arc Ferreira da Costa, Mirela. “Analyse des aspects génétiques des lentivirus et de leurs hôtes par l’étude non invasive des primates non humains : Analysis of genetic aspects of lentivirus and their hosts with non invasive techniques of non humans primates.” 2015. Doctoral Dissertation, Montpellier. Accessed September 26, 2020. http://www.theses.fr/2015MONTT018.

MLA Handbook (7th Edition):

D'Arc Ferreira da Costa, Mirela. “Analyse des aspects génétiques des lentivirus et de leurs hôtes par l’étude non invasive des primates non humains : Analysis of genetic aspects of lentivirus and their hosts with non invasive techniques of non humans primates.” 2015. Web. 26 Sep 2020.

Vancouver:

D'Arc Ferreira da Costa M. Analyse des aspects génétiques des lentivirus et de leurs hôtes par l’étude non invasive des primates non humains : Analysis of genetic aspects of lentivirus and their hosts with non invasive techniques of non humans primates. [Internet] [Doctoral dissertation]. Montpellier; 2015. [cited 2020 Sep 26]. Available from: http://www.theses.fr/2015MONTT018.

Council of Science Editors:

D'Arc Ferreira da Costa M. Analyse des aspects génétiques des lentivirus et de leurs hôtes par l’étude non invasive des primates non humains : Analysis of genetic aspects of lentivirus and their hosts with non invasive techniques of non humans primates. [Doctoral Dissertation]. Montpellier; 2015. Available from: http://www.theses.fr/2015MONTT018

18. Blomgren, Sofia. Kravsammanställning samt utvärdering avbildvisningsprogramför diagnostik inom telepatologi : En fallstudiemed SIV-metoden som tillvägagångssätt.

Degree: Information Systems, 2015, Dalarna University

De flesta har i sin närhet någon som drabbats av cancer och sjukdomsfallen har ökat genom åren. Den yrkesgrupp som ställer diagnos av denna… (more)

Subjects/Keywords: requirements; viewer; evaluation; pathology; telepathology; SIV-method.; krav; bildvisningsprogram; utvärdering; patologi; telepatologi; SIV-metoden

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APA (6th Edition):

Blomgren, S. (2015). Kravsammanställning samt utvärdering avbildvisningsprogramför diagnostik inom telepatologi : En fallstudiemed SIV-metoden som tillvägagångssätt. (Thesis). Dalarna University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:du-18118

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):

Blomgren, Sofia. “Kravsammanställning samt utvärdering avbildvisningsprogramför diagnostik inom telepatologi : En fallstudiemed SIV-metoden som tillvägagångssätt.” 2015. Thesis, Dalarna University. Accessed September 26, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:du-18118.

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

MLA Handbook (7th Edition):

Blomgren, Sofia. “Kravsammanställning samt utvärdering avbildvisningsprogramför diagnostik inom telepatologi : En fallstudiemed SIV-metoden som tillvägagångssätt.” 2015. Web. 26 Sep 2020.

Vancouver:

Blomgren S. Kravsammanställning samt utvärdering avbildvisningsprogramför diagnostik inom telepatologi : En fallstudiemed SIV-metoden som tillvägagångssätt. [Internet] [Thesis]. Dalarna University; 2015. [cited 2020 Sep 26]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:du-18118.

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

Council of Science Editors:

Blomgren S. Kravsammanställning samt utvärdering avbildvisningsprogramför diagnostik inom telepatologi : En fallstudiemed SIV-metoden som tillvägagångssätt. [Thesis]. Dalarna University; 2015. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:du-18118

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

19. Gama, Lucio. Mudanças em subgrupos de monócitos durante infecção aguda pelo vírus da imunodeficiência símia (SIV); expansão de uma população inédita de células CD14+CD16- com um fenótipo atípico CCR2-.

Degree: PhD, Alergia e Imunopatologia, 2011, University of São Paulo

Monócitos podem ser classificados em três subgrupos de acordo com o nível de expressão dos marcadores CD14 e CD16. Monócitos clássicos são os mais abundantes… (more)

Subjects/Keywords: AIDS; AIDS; CCR2; CCR2; HIV; HIV; HIV-1; HIV-1; Macrófagos; Macrophages; Monócitos; Monocytes; SIV; SIV

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APA (6th Edition):

Gama, L. (2011). Mudanças em subgrupos de monócitos durante infecção aguda pelo vírus da imunodeficiência símia (SIV); expansão de uma população inédita de células CD14+CD16- com um fenótipo atípico CCR2-. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5146/tde-22092011-115312/ ;

Chicago Manual of Style (16th Edition):

Gama, Lucio. “Mudanças em subgrupos de monócitos durante infecção aguda pelo vírus da imunodeficiência símia (SIV); expansão de uma população inédita de células CD14+CD16- com um fenótipo atípico CCR2-.” 2011. Doctoral Dissertation, University of São Paulo. Accessed September 26, 2020. http://www.teses.usp.br/teses/disponiveis/5/5146/tde-22092011-115312/ ;.

MLA Handbook (7th Edition):

Gama, Lucio. “Mudanças em subgrupos de monócitos durante infecção aguda pelo vírus da imunodeficiência símia (SIV); expansão de uma população inédita de células CD14+CD16- com um fenótipo atípico CCR2-.” 2011. Web. 26 Sep 2020.

Vancouver:

Gama L. Mudanças em subgrupos de monócitos durante infecção aguda pelo vírus da imunodeficiência símia (SIV); expansão de uma população inédita de células CD14+CD16- com um fenótipo atípico CCR2-. [Internet] [Doctoral dissertation]. University of São Paulo; 2011. [cited 2020 Sep 26]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5146/tde-22092011-115312/ ;.

Council of Science Editors:

Gama L. Mudanças em subgrupos de monócitos durante infecção aguda pelo vírus da imunodeficiência símia (SIV); expansão de uma população inédita de células CD14+CD16- com um fenótipo atípico CCR2-. [Doctoral Dissertation]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/5/5146/tde-22092011-115312/ ;


Freie Universität Berlin

20. Gabriel, Benjamin. An analysis of the protective mechanism induced by live attenuated simian immunodeficiency viruses.

Degree: 2014, Freie Universität Berlin

 Thus far, attenuated viruses demonstrated the most successful protection against challenges with SIV, but despite major efforts, the mechanism of protection is still unknown. There… (more)

Subjects/Keywords: attenuated SIV; live attenuated SIV; SIVmac239 challenge; delta-nef; vaccination; 500 Naturwissenschaften und Mathematik; 500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie

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APA (6th Edition):

Gabriel, B. (2014). An analysis of the protective mechanism induced by live attenuated simian immunodeficiency viruses. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-7827

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):

Gabriel, Benjamin. “An analysis of the protective mechanism induced by live attenuated simian immunodeficiency viruses.” 2014. Thesis, Freie Universität Berlin. Accessed September 26, 2020. http://dx.doi.org/10.17169/refubium-7827.

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

MLA Handbook (7th Edition):

Gabriel, Benjamin. “An analysis of the protective mechanism induced by live attenuated simian immunodeficiency viruses.” 2014. Web. 26 Sep 2020.

Vancouver:

Gabriel B. An analysis of the protective mechanism induced by live attenuated simian immunodeficiency viruses. [Internet] [Thesis]. Freie Universität Berlin; 2014. [cited 2020 Sep 26]. Available from: http://dx.doi.org/10.17169/refubium-7827.

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

Council of Science Editors:

Gabriel B. An analysis of the protective mechanism induced by live attenuated simian immunodeficiency viruses. [Thesis]. Freie Universität Berlin; 2014. Available from: http://dx.doi.org/10.17169/refubium-7827

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

21. Alaoui, Lamine. Etude de la dynamique de l’axe inhibiteur LILRB2/CMH-I et de sa régulation au cours de l’infection par le VIH/SIV : Dynamic and regulation of LILRB2/MHC-I inhibitory axis during HIV/SIV infection.

Degree: Docteur es, Immunologie, 2017, Université Paris-Saclay (ComUE)

Les cellules dendritiques classiques (cDC) jouent un rôle crucial dans l’efficacité des réponses immunitaires précoces conduisant au contrôle ou à la persistance virale. A cet… (more)

Subjects/Keywords: Leukocyte Immunoglobulin-Like Receptors (LILRs); Hiv/siv; Réponse immunitaires Innée; Leukocyte Immunoglobulin-Like Receptors (LILRs; Hiv/siv; Innate Immune Responses

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APA (6th Edition):

Alaoui, L. (2017). Etude de la dynamique de l’axe inhibiteur LILRB2/CMH-I et de sa régulation au cours de l’infection par le VIH/SIV : Dynamic and regulation of LILRB2/MHC-I inhibitory axis during HIV/SIV infection. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2017SACLS374

Chicago Manual of Style (16th Edition):

Alaoui, Lamine. “Etude de la dynamique de l’axe inhibiteur LILRB2/CMH-I et de sa régulation au cours de l’infection par le VIH/SIV : Dynamic and regulation of LILRB2/MHC-I inhibitory axis during HIV/SIV infection.” 2017. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed September 26, 2020. http://www.theses.fr/2017SACLS374.

MLA Handbook (7th Edition):

Alaoui, Lamine. “Etude de la dynamique de l’axe inhibiteur LILRB2/CMH-I et de sa régulation au cours de l’infection par le VIH/SIV : Dynamic and regulation of LILRB2/MHC-I inhibitory axis during HIV/SIV infection.” 2017. Web. 26 Sep 2020.

Vancouver:

Alaoui L. Etude de la dynamique de l’axe inhibiteur LILRB2/CMH-I et de sa régulation au cours de l’infection par le VIH/SIV : Dynamic and regulation of LILRB2/MHC-I inhibitory axis during HIV/SIV infection. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2017. [cited 2020 Sep 26]. Available from: http://www.theses.fr/2017SACLS374.

Council of Science Editors:

Alaoui L. Etude de la dynamique de l’axe inhibiteur LILRB2/CMH-I et de sa régulation au cours de l’infection par le VIH/SIV : Dynamic and regulation of LILRB2/MHC-I inhibitory axis during HIV/SIV infection. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2017. Available from: http://www.theses.fr/2017SACLS374

22. Lemaitre, Julien. Heterogeneity of polymorphonuclear neutrophils in HIV-1 infection. Study of SIV-infected cynomolgus macaque model. : Hétérogénéité des polynucléaires neutrophiles dans l'infection par le VIH-1.Etude du modèle macaque cynomolgus infecté par le SIV.

Degree: Docteur es, Immunologie, 2019, Université Paris-Saclay (ComUE)

La persistance du VIH-1 est associée au maintien de l’inflammation chronique chez les patients infectés, malgré la mise en place de combinaison de traitements antirétroviraux.… (more)

Subjects/Keywords: Immunité innée; Vih-1; Cellules myéloïdes; Inflammation chronique; Primate non humain; Siv; Innate immunity; Hiv; Neutrophils; Chronic inflammation; Nonhuman primate; Siv

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APA (6th Edition):

Lemaitre, J. (2019). Heterogeneity of polymorphonuclear neutrophils in HIV-1 infection. Study of SIV-infected cynomolgus macaque model. : Hétérogénéité des polynucléaires neutrophiles dans l'infection par le VIH-1.Etude du modèle macaque cynomolgus infecté par le SIV. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2019SACLS267

Chicago Manual of Style (16th Edition):

Lemaitre, Julien. “Heterogeneity of polymorphonuclear neutrophils in HIV-1 infection. Study of SIV-infected cynomolgus macaque model. : Hétérogénéité des polynucléaires neutrophiles dans l'infection par le VIH-1.Etude du modèle macaque cynomolgus infecté par le SIV.” 2019. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed September 26, 2020. http://www.theses.fr/2019SACLS267.

MLA Handbook (7th Edition):

Lemaitre, Julien. “Heterogeneity of polymorphonuclear neutrophils in HIV-1 infection. Study of SIV-infected cynomolgus macaque model. : Hétérogénéité des polynucléaires neutrophiles dans l'infection par le VIH-1.Etude du modèle macaque cynomolgus infecté par le SIV.” 2019. Web. 26 Sep 2020.

Vancouver:

Lemaitre J. Heterogeneity of polymorphonuclear neutrophils in HIV-1 infection. Study of SIV-infected cynomolgus macaque model. : Hétérogénéité des polynucléaires neutrophiles dans l'infection par le VIH-1.Etude du modèle macaque cynomolgus infecté par le SIV. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2019. [cited 2020 Sep 26]. Available from: http://www.theses.fr/2019SACLS267.

Council of Science Editors:

Lemaitre J. Heterogeneity of polymorphonuclear neutrophils in HIV-1 infection. Study of SIV-infected cynomolgus macaque model. : Hétérogénéité des polynucléaires neutrophiles dans l'infection par le VIH-1.Etude du modèle macaque cynomolgus infecté par le SIV. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2019. Available from: http://www.theses.fr/2019SACLS267


University of Pennsylvania

23. Riddick, Nadeene E. A Novel CCR5 Mutation in Sooty Mangabeys Reveals SIVsmm Infection of CCR5-null Natural Hosts: Examining the Potential Roles of Alternative Entry Pathways in HIV and SIV Infection.

Degree: 2012, University of Pennsylvania

 Natural hosts of SIV, such as sooty mangabeys (SM), maintain high levels of virus replication, but do not typically develop CD4+ T cell loss and… (more)

Subjects/Keywords: alternative; CCR5; coreceptors; HIV; mutants; SIV; Molecular Biology; Virology

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APA (6th Edition):

Riddick, N. E. (2012). A Novel CCR5 Mutation in Sooty Mangabeys Reveals SIVsmm Infection of CCR5-null Natural Hosts: Examining the Potential Roles of Alternative Entry Pathways in HIV and SIV Infection. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/566

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):

Riddick, Nadeene E. “A Novel CCR5 Mutation in Sooty Mangabeys Reveals SIVsmm Infection of CCR5-null Natural Hosts: Examining the Potential Roles of Alternative Entry Pathways in HIV and SIV Infection.” 2012. Thesis, University of Pennsylvania. Accessed September 26, 2020. https://repository.upenn.edu/edissertations/566.

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

MLA Handbook (7th Edition):

Riddick, Nadeene E. “A Novel CCR5 Mutation in Sooty Mangabeys Reveals SIVsmm Infection of CCR5-null Natural Hosts: Examining the Potential Roles of Alternative Entry Pathways in HIV and SIV Infection.” 2012. Web. 26 Sep 2020.

Vancouver:

Riddick NE. A Novel CCR5 Mutation in Sooty Mangabeys Reveals SIVsmm Infection of CCR5-null Natural Hosts: Examining the Potential Roles of Alternative Entry Pathways in HIV and SIV Infection. [Internet] [Thesis]. University of Pennsylvania; 2012. [cited 2020 Sep 26]. Available from: https://repository.upenn.edu/edissertations/566.

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

Council of Science Editors:

Riddick NE. A Novel CCR5 Mutation in Sooty Mangabeys Reveals SIVsmm Infection of CCR5-null Natural Hosts: Examining the Potential Roles of Alternative Entry Pathways in HIV and SIV Infection. [Thesis]. University of Pennsylvania; 2012. Available from: https://repository.upenn.edu/edissertations/566

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


University of Pennsylvania

24. Wetzel, Katherine. Widespread Use Of Cxcr6 For Entry By Natural Host Sivs: Implications For Cell Targeting And Infection Outcome.

Degree: 2017, University of Pennsylvania

 Natural hosts of simian immunodeficiency virus (SIV) are African primates that have coevolved with species-species SIVs and do not progress to AIDS despite high viral… (more)

Subjects/Keywords: Coreceptor; CXCR6; Simian Immunodeficiency Virus; SIV Natural Host; Virus Entry; Virology

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

APA (6th Edition):

Wetzel, K. (2017). Widespread Use Of Cxcr6 For Entry By Natural Host Sivs: Implications For Cell Targeting And Infection Outcome. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2793

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):

Wetzel, Katherine. “Widespread Use Of Cxcr6 For Entry By Natural Host Sivs: Implications For Cell Targeting And Infection Outcome.” 2017. Thesis, University of Pennsylvania. Accessed September 26, 2020. https://repository.upenn.edu/edissertations/2793.

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

MLA Handbook (7th Edition):

Wetzel, Katherine. “Widespread Use Of Cxcr6 For Entry By Natural Host Sivs: Implications For Cell Targeting And Infection Outcome.” 2017. Web. 26 Sep 2020.

Vancouver:

Wetzel K. Widespread Use Of Cxcr6 For Entry By Natural Host Sivs: Implications For Cell Targeting And Infection Outcome. [Internet] [Thesis]. University of Pennsylvania; 2017. [cited 2020 Sep 26]. Available from: https://repository.upenn.edu/edissertations/2793.

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

Council of Science Editors:

Wetzel K. Widespread Use Of Cxcr6 For Entry By Natural Host Sivs: Implications For Cell Targeting And Infection Outcome. [Thesis]. University of Pennsylvania; 2017. Available from: https://repository.upenn.edu/edissertations/2793

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


Boston University

25. Alcoreza, Oscar. Cleavage site compensatory substitutions partially restore fitness to simian immunodeficiency virus variants.

Degree: MS, Medical Sciences, 2015, Boston University

 The human immunodeficiency virus is presently one of the most significant global health issues to date, with a disease burden that encumbers developing and developed… (more)

Subjects/Keywords: Virology; Fitness; HIV; SIV; Vaccine; Functional cure; Protease cleavage site

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APA (6th Edition):

Alcoreza, O. (2015). Cleavage site compensatory substitutions partially restore fitness to simian immunodeficiency virus variants. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/16060

Chicago Manual of Style (16th Edition):

Alcoreza, Oscar. “Cleavage site compensatory substitutions partially restore fitness to simian immunodeficiency virus variants.” 2015. Masters Thesis, Boston University. Accessed September 26, 2020. http://hdl.handle.net/2144/16060.

MLA Handbook (7th Edition):

Alcoreza, Oscar. “Cleavage site compensatory substitutions partially restore fitness to simian immunodeficiency virus variants.” 2015. Web. 26 Sep 2020.

Vancouver:

Alcoreza O. Cleavage site compensatory substitutions partially restore fitness to simian immunodeficiency virus variants. [Internet] [Masters thesis]. Boston University; 2015. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/2144/16060.

Council of Science Editors:

Alcoreza O. Cleavage site compensatory substitutions partially restore fitness to simian immunodeficiency virus variants. [Masters Thesis]. Boston University; 2015. Available from: http://hdl.handle.net/2144/16060

26. Millet, Antoine. Caractérisation quantitative et génétique de la dynamique sanguine et tissulaire du virus de l'immunodéficience simienne chez le macaque cynomolgus en histoire naturelle : Quantitative and genetic characterization of simian immunodeficiency virus dynamics in blood and tissues of cynomolgus macaque during natural history.

Degree: Docteur es, Microbiologie, 2018, Sorbonne Paris Cité

 L'infection par le Virus de l'Immunodéficience Simienne (SIV) persiste dans l'organisme en raison des cellules infectées contenant le génome viral intégré. Ces cellules dites «… (more)

Subjects/Keywords: SIV; Histoire naturelle; Contrôleurs; Primo-infection; Réservoirs; Adn siv; Activité transcriptionnelle; Variants et diversité; Ngs; Bio-Informatiques; SIV; Primo-infection; Natural history; Controllers; Reservoirs; Siv dna; Transcriptional activity; Variants and diversity; Ngs; Bioinformatics; 616.979 2

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

APA (6th Edition):

Millet, A. (2018). Caractérisation quantitative et génétique de la dynamique sanguine et tissulaire du virus de l'immunodéficience simienne chez le macaque cynomolgus en histoire naturelle : Quantitative and genetic characterization of simian immunodeficiency virus dynamics in blood and tissues of cynomolgus macaque during natural history. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2018USPCB131

Chicago Manual of Style (16th Edition):

Millet, Antoine. “Caractérisation quantitative et génétique de la dynamique sanguine et tissulaire du virus de l'immunodéficience simienne chez le macaque cynomolgus en histoire naturelle : Quantitative and genetic characterization of simian immunodeficiency virus dynamics in blood and tissues of cynomolgus macaque during natural history.” 2018. Doctoral Dissertation, Sorbonne Paris Cité. Accessed September 26, 2020. http://www.theses.fr/2018USPCB131.

MLA Handbook (7th Edition):

Millet, Antoine. “Caractérisation quantitative et génétique de la dynamique sanguine et tissulaire du virus de l'immunodéficience simienne chez le macaque cynomolgus en histoire naturelle : Quantitative and genetic characterization of simian immunodeficiency virus dynamics in blood and tissues of cynomolgus macaque during natural history.” 2018. Web. 26 Sep 2020.

Vancouver:

Millet A. Caractérisation quantitative et génétique de la dynamique sanguine et tissulaire du virus de l'immunodéficience simienne chez le macaque cynomolgus en histoire naturelle : Quantitative and genetic characterization of simian immunodeficiency virus dynamics in blood and tissues of cynomolgus macaque during natural history. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2018. [cited 2020 Sep 26]. Available from: http://www.theses.fr/2018USPCB131.

Council of Science Editors:

Millet A. Caractérisation quantitative et génétique de la dynamique sanguine et tissulaire du virus de l'immunodéficience simienne chez le macaque cynomolgus en histoire naturelle : Quantitative and genetic characterization of simian immunodeficiency virus dynamics in blood and tissues of cynomolgus macaque during natural history. [Doctoral Dissertation]. Sorbonne Paris Cité; 2018. Available from: http://www.theses.fr/2018USPCB131


The Ohio State University

27. Zhang, Jian Chao. HIV-1/SIV Neutralizing Antibody Gene Delivery: A Novel Vaccination Approach.

Degree: PhD, Biophysics, 2009, The Ohio State University

  The human immunodeficiency virus (HIV) is the causative agent of acquired immunodeficiency syndrome (AIDS). Since there is no cure, creating an efficacious, safe, and… (more)

Subjects/Keywords: Biomedical Research; HIV-1/SIV vaccine; neutralizing antibody; rAAV

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

APA (6th Edition):

Zhang, J. C. (2009). HIV-1/SIV Neutralizing Antibody Gene Delivery: A Novel Vaccination Approach. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1237924213

Chicago Manual of Style (16th Edition):

Zhang, Jian Chao. “HIV-1/SIV Neutralizing Antibody Gene Delivery: A Novel Vaccination Approach.” 2009. Doctoral Dissertation, The Ohio State University. Accessed September 26, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1237924213.

MLA Handbook (7th Edition):

Zhang, Jian Chao. “HIV-1/SIV Neutralizing Antibody Gene Delivery: A Novel Vaccination Approach.” 2009. Web. 26 Sep 2020.

Vancouver:

Zhang JC. HIV-1/SIV Neutralizing Antibody Gene Delivery: A Novel Vaccination Approach. [Internet] [Doctoral dissertation]. The Ohio State University; 2009. [cited 2020 Sep 26]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1237924213.

Council of Science Editors:

Zhang JC. HIV-1/SIV Neutralizing Antibody Gene Delivery: A Novel Vaccination Approach. [Doctoral Dissertation]. The Ohio State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1237924213


Universiteit Utrecht

28. Groot, N.G. de. A selective sweep in chimpanzees : is SIV the culprit?.

Degree: 2010, Universiteit Utrecht

 The human immunodeficiency virus type 1 (HIV-1) is a major threat to mankind, as most infected individuals develop a lethal disease called acquired immunodeficiency syndrome… (more)

Subjects/Keywords: Biologie; AIDS; chimpanzees; evolution; HIV; HLA; MHC; MIC; selective sweep; SIV

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

APA (6th Edition):

Groot, N. G. d. (2010). A selective sweep in chimpanzees : is SIV the culprit?. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/179547

Chicago Manual of Style (16th Edition):

Groot, N G de. “A selective sweep in chimpanzees : is SIV the culprit?.” 2010. Doctoral Dissertation, Universiteit Utrecht. Accessed September 26, 2020. http://dspace.library.uu.nl:8080/handle/1874/179547.

MLA Handbook (7th Edition):

Groot, N G de. “A selective sweep in chimpanzees : is SIV the culprit?.” 2010. Web. 26 Sep 2020.

Vancouver:

Groot NGd. A selective sweep in chimpanzees : is SIV the culprit?. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2010. [cited 2020 Sep 26]. Available from: http://dspace.library.uu.nl:8080/handle/1874/179547.

Council of Science Editors:

Groot NGd. A selective sweep in chimpanzees : is SIV the culprit?. [Doctoral Dissertation]. Universiteit Utrecht; 2010. Available from: http://dspace.library.uu.nl:8080/handle/1874/179547


Harvard University

29. Schafer, Jamie Lynn. Rhesus macaque KIR recognition of MHC class I molecules: Ligand identification and modulation of interaction by SIV peptides.

Degree: PhD, Biology: Medical Sciences, Division of, 2014, Harvard University

 Natural killer (NK) cells can kill virus-infected cells without prior antigenic exposure, and are therefore important for controlling viral replication prior to the onset of… (more)

Subjects/Keywords: Virology; Immunology; KIR; MHC class I; NK cell; Rhesus macaque; SIV

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

APA (6th Edition):

Schafer, J. L. (2014). Rhesus macaque KIR recognition of MHC class I molecules: Ligand identification and modulation of interaction by SIV peptides. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274520

Chicago Manual of Style (16th Edition):

Schafer, Jamie Lynn. “Rhesus macaque KIR recognition of MHC class I molecules: Ligand identification and modulation of interaction by SIV peptides.” 2014. Doctoral Dissertation, Harvard University. Accessed September 26, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274520.

MLA Handbook (7th Edition):

Schafer, Jamie Lynn. “Rhesus macaque KIR recognition of MHC class I molecules: Ligand identification and modulation of interaction by SIV peptides.” 2014. Web. 26 Sep 2020.

Vancouver:

Schafer JL. Rhesus macaque KIR recognition of MHC class I molecules: Ligand identification and modulation of interaction by SIV peptides. [Internet] [Doctoral dissertation]. Harvard University; 2014. [cited 2020 Sep 26]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274520.

Council of Science Editors:

Schafer JL. Rhesus macaque KIR recognition of MHC class I molecules: Ligand identification and modulation of interaction by SIV peptides. [Doctoral Dissertation]. Harvard University; 2014. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274520

30. F. Calascibetta. ANALYSIS OF VIRAL RESERVOIRS IN CHRONICALLY SIV-INFECTED SOOTY MANGABEYS TREATED WITH COMBINATION ANTIRETROVIRAL THERAPY (CART).

Degree: 2015, Università degli Studi di Milano

 Background: Human Immunodeficiency Virus (HIV), the causative pathogen of Acquired Immunodeficiency Syndrome (AIDS), continues to be a major global public health issue. Although, potent antiretroviral… (more)

Subjects/Keywords: SIV; HIV; Persistence; Functional Cure; Settore MED/04 - Patologia Generale

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

APA (6th Edition):

Calascibetta, F. (2015). ANALYSIS OF VIRAL RESERVOIRS IN CHRONICALLY SIV-INFECTED SOOTY MANGABEYS TREATED WITH COMBINATION ANTIRETROVIRAL THERAPY (CART). (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/252682

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):

Calascibetta, F.. “ANALYSIS OF VIRAL RESERVOIRS IN CHRONICALLY SIV-INFECTED SOOTY MANGABEYS TREATED WITH COMBINATION ANTIRETROVIRAL THERAPY (CART).” 2015. Thesis, Università degli Studi di Milano. Accessed September 26, 2020. http://hdl.handle.net/2434/252682.

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

MLA Handbook (7th Edition):

Calascibetta, F.. “ANALYSIS OF VIRAL RESERVOIRS IN CHRONICALLY SIV-INFECTED SOOTY MANGABEYS TREATED WITH COMBINATION ANTIRETROVIRAL THERAPY (CART).” 2015. Web. 26 Sep 2020.

Vancouver:

Calascibetta F. ANALYSIS OF VIRAL RESERVOIRS IN CHRONICALLY SIV-INFECTED SOOTY MANGABEYS TREATED WITH COMBINATION ANTIRETROVIRAL THERAPY (CART). [Internet] [Thesis]. Università degli Studi di Milano; 2015. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/2434/252682.

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

Council of Science Editors:

Calascibetta F. ANALYSIS OF VIRAL RESERVOIRS IN CHRONICALLY SIV-INFECTED SOOTY MANGABEYS TREATED WITH COMBINATION ANTIRETROVIRAL THERAPY (CART). [Thesis]. Università degli Studi di Milano; 2015. Available from: http://hdl.handle.net/2434/252682

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

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