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You searched for subject:(Cytomegalovirus). Showing records 1 – 30 of 87 total matches.

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University of California – Berkeley

1. Yang, Edward. Proteomic Study of Human Cytomegalovirus Using an Epitope Tag System.

Degree: Comparative Biochemistry, 2011, University of California – Berkeley

 Human Cytomegalovirus (HCMV) is a ubiquitous pathogen that can cause significant morbidity in neonates and immunodeficient individuals such as, AIDS patience and organ transplant recipients.… (more)

Subjects/Keywords: Virology; Cytomegalovirus

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APA (6th Edition):

Yang, E. (2011). Proteomic Study of Human Cytomegalovirus Using an Epitope Tag System. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/4kk5m0jc

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):

Yang, Edward. “Proteomic Study of Human Cytomegalovirus Using an Epitope Tag System.” 2011. Thesis, University of California – Berkeley. Accessed November 19, 2019. http://www.escholarship.org/uc/item/4kk5m0jc.

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

MLA Handbook (7th Edition):

Yang, Edward. “Proteomic Study of Human Cytomegalovirus Using an Epitope Tag System.” 2011. Web. 19 Nov 2019.

Vancouver:

Yang E. Proteomic Study of Human Cytomegalovirus Using an Epitope Tag System. [Internet] [Thesis]. University of California – Berkeley; 2011. [cited 2019 Nov 19]. Available from: http://www.escholarship.org/uc/item/4kk5m0jc.

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

Council of Science Editors:

Yang E. Proteomic Study of Human Cytomegalovirus Using an Epitope Tag System. [Thesis]. University of California – Berkeley; 2011. Available from: http://www.escholarship.org/uc/item/4kk5m0jc

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


Oklahoma State University

2. Neubauer, Susan Rae. Characterization of the Genome of Baboon Cytomegalovirus Strain (Ocom4-37) Isolated from the Olive Baboon, Papio Cynocephalus Anubis.

Degree: Department of Biochemistry and Molecular Biology, 2011, Oklahoma State University

 This project involved cloning, sequencing, and analyzing the genome of baboon cytomegalovirus (BaCMV) strain OCOM4-37. After isolation, cloning and sequencing the coding sequence of the… (more)

Subjects/Keywords: baboon; cytomegalovirus; herpesvirus

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APA (6th Edition):

Neubauer, S. R. (2011). Characterization of the Genome of Baboon Cytomegalovirus Strain (Ocom4-37) Isolated from the Olive Baboon, Papio Cynocephalus Anubis. (Thesis). Oklahoma State University. Retrieved from http://hdl.handle.net/11244/6664

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):

Neubauer, Susan Rae. “Characterization of the Genome of Baboon Cytomegalovirus Strain (Ocom4-37) Isolated from the Olive Baboon, Papio Cynocephalus Anubis.” 2011. Thesis, Oklahoma State University. Accessed November 19, 2019. http://hdl.handle.net/11244/6664.

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

MLA Handbook (7th Edition):

Neubauer, Susan Rae. “Characterization of the Genome of Baboon Cytomegalovirus Strain (Ocom4-37) Isolated from the Olive Baboon, Papio Cynocephalus Anubis.” 2011. Web. 19 Nov 2019.

Vancouver:

Neubauer SR. Characterization of the Genome of Baboon Cytomegalovirus Strain (Ocom4-37) Isolated from the Olive Baboon, Papio Cynocephalus Anubis. [Internet] [Thesis]. Oklahoma State University; 2011. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/11244/6664.

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

Council of Science Editors:

Neubauer SR. Characterization of the Genome of Baboon Cytomegalovirus Strain (Ocom4-37) Isolated from the Olive Baboon, Papio Cynocephalus Anubis. [Thesis]. Oklahoma State University; 2011. Available from: http://hdl.handle.net/11244/6664

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


University of Cincinnati

3. Stadler, Laura Patricia. Seroprevalence and Risk Factor Analysis of Cytomegalovirus (CMV) Infections in Adolescent Females.

Degree: MS, Medicine : Epidemiology (Environmental Health), 2007, University of Cincinnati

  Background: Cytomegalovirus (CMV) is one of the leading causes of birth defects and childhood disability in the US. Methods: To determine the CMV seroprevalence… (more)

Subjects/Keywords: Epidemiology; Cytomegalovirus; Seroprevalence; Adolescent females

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APA (6th Edition):

Stadler, L. P. (2007). Seroprevalence and Risk Factor Analysis of Cytomegalovirus (CMV) Infections in Adolescent Females. (Masters Thesis). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1172863532

Chicago Manual of Style (16th Edition):

Stadler, Laura Patricia. “Seroprevalence and Risk Factor Analysis of Cytomegalovirus (CMV) Infections in Adolescent Females.” 2007. Masters Thesis, University of Cincinnati. Accessed November 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1172863532.

MLA Handbook (7th Edition):

Stadler, Laura Patricia. “Seroprevalence and Risk Factor Analysis of Cytomegalovirus (CMV) Infections in Adolescent Females.” 2007. Web. 19 Nov 2019.

Vancouver:

Stadler LP. Seroprevalence and Risk Factor Analysis of Cytomegalovirus (CMV) Infections in Adolescent Females. [Internet] [Masters thesis]. University of Cincinnati; 2007. [cited 2019 Nov 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1172863532.

Council of Science Editors:

Stadler LP. Seroprevalence and Risk Factor Analysis of Cytomegalovirus (CMV) Infections in Adolescent Females. [Masters Thesis]. University of Cincinnati; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1172863532


The Ohio State University

4. Machesky, Nicholas John. The modulation of sphingolipids by human cytomegalovirus and its influence on viral protein accumulation and growth.

Degree: PhD, Integrated Biomedical Science, 2007, The Ohio State University

 Human cytomegalovirus (HCMV) is a beta-herpes virus which can cause serious disease and even death in congenitally-infected infants and in immunocompromised individuals or immunosuppressed transplant… (more)

Subjects/Keywords: sphingolipids; cytomegalovirus; sphingosine kinase; S1P

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APA (6th Edition):

Machesky, N. J. (2007). The modulation of sphingolipids by human cytomegalovirus and its influence on viral protein accumulation and growth. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1181753517

Chicago Manual of Style (16th Edition):

Machesky, Nicholas John. “The modulation of sphingolipids by human cytomegalovirus and its influence on viral protein accumulation and growth.” 2007. Doctoral Dissertation, The Ohio State University. Accessed November 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1181753517.

MLA Handbook (7th Edition):

Machesky, Nicholas John. “The modulation of sphingolipids by human cytomegalovirus and its influence on viral protein accumulation and growth.” 2007. Web. 19 Nov 2019.

Vancouver:

Machesky NJ. The modulation of sphingolipids by human cytomegalovirus and its influence on viral protein accumulation and growth. [Internet] [Doctoral dissertation]. The Ohio State University; 2007. [cited 2019 Nov 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1181753517.

Council of Science Editors:

Machesky NJ. The modulation of sphingolipids by human cytomegalovirus and its influence on viral protein accumulation and growth. [Doctoral Dissertation]. The Ohio State University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1181753517


University of Southern California

5. Abichaker, George. Cytomegalovirus induced amelogenesis imperfecta.

Degree: MS, Cranio-Facial Biology, 2012, University of Southern California

 BACKGROUND: Cytomegalovirus (CMV) is one of the most common causes of major birth defects in humans. Of the approximately 8400 children born each year in… (more)

Subjects/Keywords: cytomegalovirus; cmv; tooth; amelogenesis imperfecta

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APA (6th Edition):

Abichaker, G. (2012). Cytomegalovirus induced amelogenesis imperfecta. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/30882/rec/1750

Chicago Manual of Style (16th Edition):

Abichaker, George. “Cytomegalovirus induced amelogenesis imperfecta.” 2012. Masters Thesis, University of Southern California. Accessed November 19, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/30882/rec/1750.

MLA Handbook (7th Edition):

Abichaker, George. “Cytomegalovirus induced amelogenesis imperfecta.” 2012. Web. 19 Nov 2019.

Vancouver:

Abichaker G. Cytomegalovirus induced amelogenesis imperfecta. [Internet] [Masters thesis]. University of Southern California; 2012. [cited 2019 Nov 19]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/30882/rec/1750.

Council of Science Editors:

Abichaker G. Cytomegalovirus induced amelogenesis imperfecta. [Masters Thesis]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/30882/rec/1750


Princeton University

6. Jean Beltran, Pierre Michel. CHARACTERIZATION OF THE GLOBAL MODULATION OF ORGANELLES CAUSED BY VIRAL INFECTION .

Degree: PhD, 2018, Princeton University

 The cell is a complex system that is organized into multiple subcellular compartments known as organelles. Viruses, obligate intracellular pathogens, exploit organelle functions to facilitate… (more)

Subjects/Keywords: cytomegalovirus; HCMV; Organelles; proteomics; Virus

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APA (6th Edition):

Jean Beltran, P. M. (2018). CHARACTERIZATION OF THE GLOBAL MODULATION OF ORGANELLES CAUSED BY VIRAL INFECTION . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01tq57nt807

Chicago Manual of Style (16th Edition):

Jean Beltran, Pierre Michel. “CHARACTERIZATION OF THE GLOBAL MODULATION OF ORGANELLES CAUSED BY VIRAL INFECTION .” 2018. Doctoral Dissertation, Princeton University. Accessed November 19, 2019. http://arks.princeton.edu/ark:/88435/dsp01tq57nt807.

MLA Handbook (7th Edition):

Jean Beltran, Pierre Michel. “CHARACTERIZATION OF THE GLOBAL MODULATION OF ORGANELLES CAUSED BY VIRAL INFECTION .” 2018. Web. 19 Nov 2019.

Vancouver:

Jean Beltran PM. CHARACTERIZATION OF THE GLOBAL MODULATION OF ORGANELLES CAUSED BY VIRAL INFECTION . [Internet] [Doctoral dissertation]. Princeton University; 2018. [cited 2019 Nov 19]. Available from: http://arks.princeton.edu/ark:/88435/dsp01tq57nt807.

Council of Science Editors:

Jean Beltran PM. CHARACTERIZATION OF THE GLOBAL MODULATION OF ORGANELLES CAUSED BY VIRAL INFECTION . [Doctoral Dissertation]. Princeton University; 2018. Available from: http://arks.princeton.edu/ark:/88435/dsp01tq57nt807


University of California – Berkeley

7. Umamoto, Sean. Global Analysis of Murine Cytomegalovirus Open Reading Frames Using Yeast Two-Hybrid and Growth Phenotype Analysis.

Degree: Comparative Biochemistry, 2011, University of California – Berkeley

 Human cytomegalovirus (HCMV), a beta-herpesvirus, is an important opportunistic pathogen that primarily affects individuals with compromised or immature immune systems. It is of great significance… (more)

Subjects/Keywords: Virology; Molecular Biology; CMV; cytomegalovirus; MCMV; murine cytomegalovirus; yeast two-hybrid

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APA (6th Edition):

Umamoto, S. (2011). Global Analysis of Murine Cytomegalovirus Open Reading Frames Using Yeast Two-Hybrid and Growth Phenotype Analysis. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/0177z7vw

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):

Umamoto, Sean. “Global Analysis of Murine Cytomegalovirus Open Reading Frames Using Yeast Two-Hybrid and Growth Phenotype Analysis.” 2011. Thesis, University of California – Berkeley. Accessed November 19, 2019. http://www.escholarship.org/uc/item/0177z7vw.

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

MLA Handbook (7th Edition):

Umamoto, Sean. “Global Analysis of Murine Cytomegalovirus Open Reading Frames Using Yeast Two-Hybrid and Growth Phenotype Analysis.” 2011. Web. 19 Nov 2019.

Vancouver:

Umamoto S. Global Analysis of Murine Cytomegalovirus Open Reading Frames Using Yeast Two-Hybrid and Growth Phenotype Analysis. [Internet] [Thesis]. University of California – Berkeley; 2011. [cited 2019 Nov 19]. Available from: http://www.escholarship.org/uc/item/0177z7vw.

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

Council of Science Editors:

Umamoto S. Global Analysis of Murine Cytomegalovirus Open Reading Frames Using Yeast Two-Hybrid and Growth Phenotype Analysis. [Thesis]. University of California – Berkeley; 2011. Available from: http://www.escholarship.org/uc/item/0177z7vw

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


Georgia State University

8. Alston, Christine I. Suppressor of Cytokine Signaling (SOCS)1 and SOCS3 Stimulation during Experimental Cytomegalovirus Retinitis: Virologic, Immunologic, or Pathologic Mechanisms.

Degree: PhD, Biology, 2017, Georgia State University

  AIDS-related human cytomegalovirus (HCMV) retinitis remains the leading cause of blindness among untreated HIV/AIDS patients worldwide. Understanding the pathogenesis of this disease is essential… (more)

Subjects/Keywords: Cytomegalovirus retinitis; human cytomegalovirus (HCMV); HIV/AIDS; suppressors of cytokine signaling (SOCS); murine cytomegalovirus (MCMV); murine AIDS (MAIDS)

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APA (6th Edition):

Alston, C. I. (2017). Suppressor of Cytokine Signaling (SOCS)1 and SOCS3 Stimulation during Experimental Cytomegalovirus Retinitis: Virologic, Immunologic, or Pathologic Mechanisms. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/biology_diss/172

Chicago Manual of Style (16th Edition):

Alston, Christine I. “Suppressor of Cytokine Signaling (SOCS)1 and SOCS3 Stimulation during Experimental Cytomegalovirus Retinitis: Virologic, Immunologic, or Pathologic Mechanisms.” 2017. Doctoral Dissertation, Georgia State University. Accessed November 19, 2019. https://scholarworks.gsu.edu/biology_diss/172.

MLA Handbook (7th Edition):

Alston, Christine I. “Suppressor of Cytokine Signaling (SOCS)1 and SOCS3 Stimulation during Experimental Cytomegalovirus Retinitis: Virologic, Immunologic, or Pathologic Mechanisms.” 2017. Web. 19 Nov 2019.

Vancouver:

Alston CI. Suppressor of Cytokine Signaling (SOCS)1 and SOCS3 Stimulation during Experimental Cytomegalovirus Retinitis: Virologic, Immunologic, or Pathologic Mechanisms. [Internet] [Doctoral dissertation]. Georgia State University; 2017. [cited 2019 Nov 19]. Available from: https://scholarworks.gsu.edu/biology_diss/172.

Council of Science Editors:

Alston CI. Suppressor of Cytokine Signaling (SOCS)1 and SOCS3 Stimulation during Experimental Cytomegalovirus Retinitis: Virologic, Immunologic, or Pathologic Mechanisms. [Doctoral Dissertation]. Georgia State University; 2017. Available from: https://scholarworks.gsu.edu/biology_diss/172

9. Chapa, Travis. Murine Cytomegalovirus Encodes Proteins that Regulate Viral Late Transcription.

Degree: PhD, Biology and Biomedical Sciences: Molecular Microbiology and Microbial Pathogenesis, 2014, Washington University in St. Louis

  Human Cytomegalovirus (HCMV) is a Beta-herpesvirus that causes severe disease in immuno-compromised individuals (including AIDS patients), and is the leading viral cause of congenital… (more)

Subjects/Keywords: cytomegalovirus; late gene; M79; M92; regulation; transcription

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APA (6th Edition):

Chapa, T. (2014). Murine Cytomegalovirus Encodes Proteins that Regulate Viral Late Transcription. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/etd/1289

Chicago Manual of Style (16th Edition):

Chapa, Travis. “Murine Cytomegalovirus Encodes Proteins that Regulate Viral Late Transcription.” 2014. Doctoral Dissertation, Washington University in St. Louis. Accessed November 19, 2019. https://openscholarship.wustl.edu/etd/1289.

MLA Handbook (7th Edition):

Chapa, Travis. “Murine Cytomegalovirus Encodes Proteins that Regulate Viral Late Transcription.” 2014. Web. 19 Nov 2019.

Vancouver:

Chapa T. Murine Cytomegalovirus Encodes Proteins that Regulate Viral Late Transcription. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2014. [cited 2019 Nov 19]. Available from: https://openscholarship.wustl.edu/etd/1289.

Council of Science Editors:

Chapa T. Murine Cytomegalovirus Encodes Proteins that Regulate Viral Late Transcription. [Doctoral Dissertation]. Washington University in St. Louis; 2014. Available from: https://openscholarship.wustl.edu/etd/1289


Duke University

10. Nelson, Cody Shaw. Defining the Role of Antibodies in Protection Against Cytomegalovirus Acquisition and Congenital Disease for Rational Vaccine Design .

Degree: 2018, Duke University

  Human cytomegalovirus (HCMV) is the most common cause of congenital infection worldwide, impacting 1 in 150 live-born infants. Children afflicted by congenital HCMV frequently… (more)

Subjects/Keywords: Immunology; Virology; Microbiology; Antibodies; Cytomegalovirus; Vaccines

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APA (6th Edition):

Nelson, C. S. (2018). Defining the Role of Antibodies in Protection Against Cytomegalovirus Acquisition and Congenital Disease for Rational Vaccine Design . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/17434

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):

Nelson, Cody Shaw. “Defining the Role of Antibodies in Protection Against Cytomegalovirus Acquisition and Congenital Disease for Rational Vaccine Design .” 2018. Thesis, Duke University. Accessed November 19, 2019. http://hdl.handle.net/10161/17434.

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

MLA Handbook (7th Edition):

Nelson, Cody Shaw. “Defining the Role of Antibodies in Protection Against Cytomegalovirus Acquisition and Congenital Disease for Rational Vaccine Design .” 2018. Web. 19 Nov 2019.

Vancouver:

Nelson CS. Defining the Role of Antibodies in Protection Against Cytomegalovirus Acquisition and Congenital Disease for Rational Vaccine Design . [Internet] [Thesis]. Duke University; 2018. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/10161/17434.

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

Council of Science Editors:

Nelson CS. Defining the Role of Antibodies in Protection Against Cytomegalovirus Acquisition and Congenital Disease for Rational Vaccine Design . [Thesis]. Duke University; 2018. Available from: http://hdl.handle.net/10161/17434

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


Virginia Commonwealth University

11. Saccoccio, Frances. CMV vaccine development based on epithelial entry mediators UL128, UL130, UL131.

Degree: PhD, Microbiology & Immunology, 2011, Virginia Commonwealth University

 Congenital cytomegalovirus infection is the leading cause of sensorineural hearing loss in the U.S. CMV vaccines developed to date do not protect the majority of… (more)

Subjects/Keywords: cytomegalovirus; vaccine; Medicine and Health Sciences

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APA (6th Edition):

Saccoccio, F. (2011). CMV vaccine development based on epithelial entry mediators UL128, UL130, UL131. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/2507

Chicago Manual of Style (16th Edition):

Saccoccio, Frances. “CMV vaccine development based on epithelial entry mediators UL128, UL130, UL131.” 2011. Doctoral Dissertation, Virginia Commonwealth University. Accessed November 19, 2019. https://scholarscompass.vcu.edu/etd/2507.

MLA Handbook (7th Edition):

Saccoccio, Frances. “CMV vaccine development based on epithelial entry mediators UL128, UL130, UL131.” 2011. Web. 19 Nov 2019.

Vancouver:

Saccoccio F. CMV vaccine development based on epithelial entry mediators UL128, UL130, UL131. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2011. [cited 2019 Nov 19]. Available from: https://scholarscompass.vcu.edu/etd/2507.

Council of Science Editors:

Saccoccio F. CMV vaccine development based on epithelial entry mediators UL128, UL130, UL131. [Doctoral Dissertation]. Virginia Commonwealth University; 2011. Available from: https://scholarscompass.vcu.edu/etd/2507


Virginia Commonwealth University

12. Bhave, Sukhada. INVESTIGATING SYNERGY BETWEEN RIBONUCLEOTIDE REDUCTASE INHIBITORS AND CMV ANTIVIRALS.

Degree: MS, Microbiology & Immunology, 2012, Virginia Commonwealth University

Cytomegalovirus (CMV) infections remain a significant problem in congenitally infected infants and immunocompromised individuals. Modest antiviral activities of currently approved drugs coupled with dose-limiting toxicities… (more)

Subjects/Keywords: cytomegalovirus; antivirals; Medicine and Health Sciences

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APA (6th Edition):

Bhave, S. (2012). INVESTIGATING SYNERGY BETWEEN RIBONUCLEOTIDE REDUCTASE INHIBITORS AND CMV ANTIVIRALS. (Thesis). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/2838

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):

Bhave, Sukhada. “INVESTIGATING SYNERGY BETWEEN RIBONUCLEOTIDE REDUCTASE INHIBITORS AND CMV ANTIVIRALS.” 2012. Thesis, Virginia Commonwealth University. Accessed November 19, 2019. https://scholarscompass.vcu.edu/etd/2838.

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

MLA Handbook (7th Edition):

Bhave, Sukhada. “INVESTIGATING SYNERGY BETWEEN RIBONUCLEOTIDE REDUCTASE INHIBITORS AND CMV ANTIVIRALS.” 2012. Web. 19 Nov 2019.

Vancouver:

Bhave S. INVESTIGATING SYNERGY BETWEEN RIBONUCLEOTIDE REDUCTASE INHIBITORS AND CMV ANTIVIRALS. [Internet] [Thesis]. Virginia Commonwealth University; 2012. [cited 2019 Nov 19]. Available from: https://scholarscompass.vcu.edu/etd/2838.

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

Council of Science Editors:

Bhave S. INVESTIGATING SYNERGY BETWEEN RIBONUCLEOTIDE REDUCTASE INHIBITORS AND CMV ANTIVIRALS. [Thesis]. Virginia Commonwealth University; 2012. Available from: https://scholarscompass.vcu.edu/etd/2838

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


University of Rochester

13. DeVito, Stefanie Renee. Contributions of Pyrimidine Biosynthesis to Viral Infection.

Degree: PhD, 2015, University of Rochester

 Human cytomegalovirus (HCMV) induces numerous changes to the host metabolic network upon infection that are critical for high-titer viral replication. We find that HCMV infection… (more)

Subjects/Keywords: Cytomegalovirus; Pyrimidine; Glycosylation; Metabolism; UDP-Sugar

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APA (6th Edition):

DeVito, S. R. (2015). Contributions of Pyrimidine Biosynthesis to Viral Infection. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/30115

Chicago Manual of Style (16th Edition):

DeVito, Stefanie Renee. “Contributions of Pyrimidine Biosynthesis to Viral Infection.” 2015. Doctoral Dissertation, University of Rochester. Accessed November 19, 2019. http://hdl.handle.net/1802/30115.

MLA Handbook (7th Edition):

DeVito, Stefanie Renee. “Contributions of Pyrimidine Biosynthesis to Viral Infection.” 2015. Web. 19 Nov 2019.

Vancouver:

DeVito SR. Contributions of Pyrimidine Biosynthesis to Viral Infection. [Internet] [Doctoral dissertation]. University of Rochester; 2015. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/1802/30115.

Council of Science Editors:

DeVito SR. Contributions of Pyrimidine Biosynthesis to Viral Infection. [Doctoral Dissertation]. University of Rochester; 2015. Available from: http://hdl.handle.net/1802/30115


University of Arizona

14. Rak, Michael A. The Role of Human Cytomegalovirus Protein UL135 in Virus Replication, Latency, and Reactivation .

Degree: 2018, University of Arizona

 Human cytomegalovirus (CMV) is a ubiquitous herpesvirus that infects the majority of the world’s population. CMV can establish a latent infection, enabling the lifelong persistence… (more)

Subjects/Keywords: Abi-1; CIN85; Cytomegalovirus; Latency; Reactivation; UL135

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APA (6th Edition):

Rak, M. A. (2018). The Role of Human Cytomegalovirus Protein UL135 in Virus Replication, Latency, and Reactivation . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/630166

Chicago Manual of Style (16th Edition):

Rak, Michael A. “The Role of Human Cytomegalovirus Protein UL135 in Virus Replication, Latency, and Reactivation .” 2018. Doctoral Dissertation, University of Arizona. Accessed November 19, 2019. http://hdl.handle.net/10150/630166.

MLA Handbook (7th Edition):

Rak, Michael A. “The Role of Human Cytomegalovirus Protein UL135 in Virus Replication, Latency, and Reactivation .” 2018. Web. 19 Nov 2019.

Vancouver:

Rak MA. The Role of Human Cytomegalovirus Protein UL135 in Virus Replication, Latency, and Reactivation . [Internet] [Doctoral dissertation]. University of Arizona; 2018. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/10150/630166.

Council of Science Editors:

Rak MA. The Role of Human Cytomegalovirus Protein UL135 in Virus Replication, Latency, and Reactivation . [Doctoral Dissertation]. University of Arizona; 2018. Available from: http://hdl.handle.net/10150/630166

15. Lagadinos, Alexander N. Human Cytomegalovirus Reprograms the Expression of Host Micro-RNAs whose Target Networks are Required for Viral Replication: A Dissertation.

Degree: Immunology and Microbiology, Microbiology and Physiological Systems, 2013, U of Massachusetts : Med

  The parasitic nature of viruses requires that they adapt to their host environment in order to persist. Herpesviruses are among the largest and most… (more)

Subjects/Keywords: Cytomegalovirus; Cytomegalovirus Infections; MicroRNAs; RNA Interference; Virus Replication; Immunology and Infectious Disease; Molecular Genetics; Virology

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APA (6th Edition):

Lagadinos, A. N. (2013). Human Cytomegalovirus Reprograms the Expression of Host Micro-RNAs whose Target Networks are Required for Viral Replication: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/683

Chicago Manual of Style (16th Edition):

Lagadinos, Alexander N. “Human Cytomegalovirus Reprograms the Expression of Host Micro-RNAs whose Target Networks are Required for Viral Replication: A Dissertation.” 2013. Doctoral Dissertation, U of Massachusetts : Med. Accessed November 19, 2019. http://escholarship.umassmed.edu/gsbs_diss/683.

MLA Handbook (7th Edition):

Lagadinos, Alexander N. “Human Cytomegalovirus Reprograms the Expression of Host Micro-RNAs whose Target Networks are Required for Viral Replication: A Dissertation.” 2013. Web. 19 Nov 2019.

Vancouver:

Lagadinos AN. Human Cytomegalovirus Reprograms the Expression of Host Micro-RNAs whose Target Networks are Required for Viral Replication: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2013. [cited 2019 Nov 19]. Available from: http://escholarship.umassmed.edu/gsbs_diss/683.

Council of Science Editors:

Lagadinos AN. Human Cytomegalovirus Reprograms the Expression of Host Micro-RNAs whose Target Networks are Required for Viral Replication: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2013. Available from: http://escholarship.umassmed.edu/gsbs_diss/683


Georgia State University

16. DUNCAN, LAUREN-ASHLEY. DETECTION OF NECROPTOSIS AND PYROPTOSIS-ASSOCIATED MOLECULES DURING EXPERIMENTAL MAIDS-RELATED CYTOMEGALOVIRUS RETINITIS.

Degree: MS, 2019, Georgia State University

  Sight threatening human cytomegalovirus (HCMV) retinitis still remains a cause for concern among AIDS patients who do not respond to or do not have… (more)

Subjects/Keywords: Necroptosis-associated molecules; Pyroptosis associated molecules; cytomegalovirus retinitis; HIV/AIDS; MAIDS; Cytomegalovirus (CMV); Cell death

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APA (6th Edition):

DUNCAN, L. (2019). DETECTION OF NECROPTOSIS AND PYROPTOSIS-ASSOCIATED MOLECULES DURING EXPERIMENTAL MAIDS-RELATED CYTOMEGALOVIRUS RETINITIS. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/biology_theses/88

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):

DUNCAN, LAUREN-ASHLEY. “DETECTION OF NECROPTOSIS AND PYROPTOSIS-ASSOCIATED MOLECULES DURING EXPERIMENTAL MAIDS-RELATED CYTOMEGALOVIRUS RETINITIS.” 2019. Thesis, Georgia State University. Accessed November 19, 2019. https://scholarworks.gsu.edu/biology_theses/88.

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

MLA Handbook (7th Edition):

DUNCAN, LAUREN-ASHLEY. “DETECTION OF NECROPTOSIS AND PYROPTOSIS-ASSOCIATED MOLECULES DURING EXPERIMENTAL MAIDS-RELATED CYTOMEGALOVIRUS RETINITIS.” 2019. Web. 19 Nov 2019.

Vancouver:

DUNCAN L. DETECTION OF NECROPTOSIS AND PYROPTOSIS-ASSOCIATED MOLECULES DURING EXPERIMENTAL MAIDS-RELATED CYTOMEGALOVIRUS RETINITIS. [Internet] [Thesis]. Georgia State University; 2019. [cited 2019 Nov 19]. Available from: https://scholarworks.gsu.edu/biology_theses/88.

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

Council of Science Editors:

DUNCAN L. DETECTION OF NECROPTOSIS AND PYROPTOSIS-ASSOCIATED MOLECULES DURING EXPERIMENTAL MAIDS-RELATED CYTOMEGALOVIRUS RETINITIS. [Thesis]. Georgia State University; 2019. Available from: https://scholarworks.gsu.edu/biology_theses/88

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


University of Florida

17. Patidar, Seema. Type D Personality, Th-1 Cytokine Levels and Cytomegalovirus Antigenemia in Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplant.

Degree: MS, Psychology - Clinical and Health Psychology, 2010, University of Florida

Cytomegalovirus (CMV) is a latent Herpes virus that may cause life-threatening illness in immune-compromised individuals. T-helper cell type 1 (Th1) cytokines, such as Interleukin-12, Interferon-gamma,… (more)

Subjects/Keywords: Blood; Cytokines; Cytomegalovirus; Disease risks; Diseases; Immunity; Personality psychology; Psychological assessment; Psychology; Psychosociology; bone, cancer, cytokines, cytomegalovirus, hsct, type

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APA (6th Edition):

Patidar, S. (2010). Type D Personality, Th-1 Cytokine Levels and Cytomegalovirus Antigenemia in Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplant. (Masters Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0041704

Chicago Manual of Style (16th Edition):

Patidar, Seema. “Type D Personality, Th-1 Cytokine Levels and Cytomegalovirus Antigenemia in Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplant.” 2010. Masters Thesis, University of Florida. Accessed November 19, 2019. http://ufdc.ufl.edu/UFE0041704.

MLA Handbook (7th Edition):

Patidar, Seema. “Type D Personality, Th-1 Cytokine Levels and Cytomegalovirus Antigenemia in Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplant.” 2010. Web. 19 Nov 2019.

Vancouver:

Patidar S. Type D Personality, Th-1 Cytokine Levels and Cytomegalovirus Antigenemia in Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplant. [Internet] [Masters thesis]. University of Florida; 2010. [cited 2019 Nov 19]. Available from: http://ufdc.ufl.edu/UFE0041704.

Council of Science Editors:

Patidar S. Type D Personality, Th-1 Cytokine Levels and Cytomegalovirus Antigenemia in Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplant. [Masters Thesis]. University of Florida; 2010. Available from: http://ufdc.ufl.edu/UFE0041704

18. Tu, Carolyn C. The roles of human cytomegalovirus US27 gene product during virus infection.

Degree: MSin Biology, Biology, 2015, University of San Francisco

  Human cytomegalovirus (HCMV) is a widespread pathogen that causes lifelong latent infection. Successful persistence of HCMV in healthy individuals involves extensive manipulation of host… (more)

Subjects/Keywords: Human cytomegalovirus; UL111A; cmvIL-10; US27; CXCR4; Biology

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APA (6th Edition):

Tu, C. C. (2015). The roles of human cytomegalovirus US27 gene product during virus infection. (Thesis). University of San Francisco. Retrieved from https://repository.usfca.edu/thes/154

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):

Tu, Carolyn C. “The roles of human cytomegalovirus US27 gene product during virus infection.” 2015. Thesis, University of San Francisco. Accessed November 19, 2019. https://repository.usfca.edu/thes/154.

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

MLA Handbook (7th Edition):

Tu, Carolyn C. “The roles of human cytomegalovirus US27 gene product during virus infection.” 2015. Web. 19 Nov 2019.

Vancouver:

Tu CC. The roles of human cytomegalovirus US27 gene product during virus infection. [Internet] [Thesis]. University of San Francisco; 2015. [cited 2019 Nov 19]. Available from: https://repository.usfca.edu/thes/154.

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

Council of Science Editors:

Tu CC. The roles of human cytomegalovirus US27 gene product during virus infection. [Thesis]. University of San Francisco; 2015. Available from: https://repository.usfca.edu/thes/154

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

19. Bishop, Robin. HCMV Promotes Breast Cancer Metastasis: Impacts of CMVIL-10 in the Tumor Microenvironment.

Degree: MS, Biology, 2013, University of San Francisco

  Human cytomegalovirus (HCMV) is a highly species-specific, common human pathogen. While a large majority of people are infected with HCMV worldwide, infection is typically… (more)

Subjects/Keywords: breast cancer; metastasis; human cytomegalovirus; HCMV; cmvIL-10; interleukin; Virology

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APA (6th Edition):

Bishop, R. (2013). HCMV Promotes Breast Cancer Metastasis: Impacts of CMVIL-10 in the Tumor Microenvironment. (Thesis). University of San Francisco. Retrieved from https://repository.usfca.edu/thes/72

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):

Bishop, Robin. “HCMV Promotes Breast Cancer Metastasis: Impacts of CMVIL-10 in the Tumor Microenvironment.” 2013. Thesis, University of San Francisco. Accessed November 19, 2019. https://repository.usfca.edu/thes/72.

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

MLA Handbook (7th Edition):

Bishop, Robin. “HCMV Promotes Breast Cancer Metastasis: Impacts of CMVIL-10 in the Tumor Microenvironment.” 2013. Web. 19 Nov 2019.

Vancouver:

Bishop R. HCMV Promotes Breast Cancer Metastasis: Impacts of CMVIL-10 in the Tumor Microenvironment. [Internet] [Thesis]. University of San Francisco; 2013. [cited 2019 Nov 19]. Available from: https://repository.usfca.edu/thes/72.

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

Council of Science Editors:

Bishop R. HCMV Promotes Breast Cancer Metastasis: Impacts of CMVIL-10 in the Tumor Microenvironment. [Thesis]. University of San Francisco; 2013. Available from: https://repository.usfca.edu/thes/72

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


University of Cincinnati

20. Morrison, Kristen M. Ex Vivo Salivary Gland Culture as a Novel System to Evaluate HCMV Infection.

Degree: MS, Medicine: Molecular Genetics, Biochemistry, and Microbiology, 2016, University of Cincinnati

 Human Cytomegalovirus (HCMV), also known as human herpesvirus 5 (HHV5), and the related rodent and non-human primate cytomegaloviruses (MCMV, RCMV and rhCMV), encode G-protein coupled… (more)

Subjects/Keywords: Molecular Biology; salivary gland; cytomegalovirus; HCMV; US28; ex vivo; culture model

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APA (6th Edition):

Morrison, K. M. (2016). Ex Vivo Salivary Gland Culture as a Novel System to Evaluate HCMV Infection. (Masters Thesis). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1470044093

Chicago Manual of Style (16th Edition):

Morrison, Kristen M. “Ex Vivo Salivary Gland Culture as a Novel System to Evaluate HCMV Infection.” 2016. Masters Thesis, University of Cincinnati. Accessed November 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1470044093.

MLA Handbook (7th Edition):

Morrison, Kristen M. “Ex Vivo Salivary Gland Culture as a Novel System to Evaluate HCMV Infection.” 2016. Web. 19 Nov 2019.

Vancouver:

Morrison KM. Ex Vivo Salivary Gland Culture as a Novel System to Evaluate HCMV Infection. [Internet] [Masters thesis]. University of Cincinnati; 2016. [cited 2019 Nov 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1470044093.

Council of Science Editors:

Morrison KM. Ex Vivo Salivary Gland Culture as a Novel System to Evaluate HCMV Infection. [Masters Thesis]. University of Cincinnati; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1470044093


Penn State University

21. Stamer, Mindy Marie. PRIMARY IN VITRO T CELL RESPONSES TO CYTOMEGALOVIRUS.

Degree: MS, Microbiology and Immunology, 2009, Penn State University

 Adoptive T cell therapy is commonly used for prophylactic and therapeutic treatment of cytomegalovirus (CMV) disease following HSC transplantation of CMV-seropositive recipients of CMV-seropositive donors.… (more)

Subjects/Keywords: T cells; adoptive T cell therapy; cytomegalovirus; T cell priming

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APA (6th Edition):

Stamer, M. M. (2009). PRIMARY IN VITRO T CELL RESPONSES TO CYTOMEGALOVIRUS. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/10539

Chicago Manual of Style (16th Edition):

Stamer, Mindy Marie. “PRIMARY IN VITRO T CELL RESPONSES TO CYTOMEGALOVIRUS.” 2009. Masters Thesis, Penn State University. Accessed November 19, 2019. https://etda.libraries.psu.edu/catalog/10539.

MLA Handbook (7th Edition):

Stamer, Mindy Marie. “PRIMARY IN VITRO T CELL RESPONSES TO CYTOMEGALOVIRUS.” 2009. Web. 19 Nov 2019.

Vancouver:

Stamer MM. PRIMARY IN VITRO T CELL RESPONSES TO CYTOMEGALOVIRUS. [Internet] [Masters thesis]. Penn State University; 2009. [cited 2019 Nov 19]. Available from: https://etda.libraries.psu.edu/catalog/10539.

Council of Science Editors:

Stamer MM. PRIMARY IN VITRO T CELL RESPONSES TO CYTOMEGALOVIRUS. [Masters Thesis]. Penn State University; 2009. Available from: https://etda.libraries.psu.edu/catalog/10539


University of California – Berkeley

22. Tokuyama, Maria. Understanding the Mechanism of Stimulatory NK-cell Ligand Expression.

Degree: Molecular & Cell Biology, 2012, University of California – Berkeley

 Natural killer (NK) cells are lymphocytes that play a major role in the elimination of virally-infected cells and tumor cells. NK cells recognize and target… (more)

Subjects/Keywords: Molecular biology; Immunology; Mouse cytomegalovirus; NK cells; NKG2D ligands; RAE-1

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APA (6th Edition):

Tokuyama, M. (2012). Understanding the Mechanism of Stimulatory NK-cell Ligand Expression. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/8f1131p6

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):

Tokuyama, Maria. “Understanding the Mechanism of Stimulatory NK-cell Ligand Expression.” 2012. Thesis, University of California – Berkeley. Accessed November 19, 2019. http://www.escholarship.org/uc/item/8f1131p6.

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

MLA Handbook (7th Edition):

Tokuyama, Maria. “Understanding the Mechanism of Stimulatory NK-cell Ligand Expression.” 2012. Web. 19 Nov 2019.

Vancouver:

Tokuyama M. Understanding the Mechanism of Stimulatory NK-cell Ligand Expression. [Internet] [Thesis]. University of California – Berkeley; 2012. [cited 2019 Nov 19]. Available from: http://www.escholarship.org/uc/item/8f1131p6.

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

Council of Science Editors:

Tokuyama M. Understanding the Mechanism of Stimulatory NK-cell Ligand Expression. [Thesis]. University of California – Berkeley; 2012. Available from: http://www.escholarship.org/uc/item/8f1131p6

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


University of Tennessee – Knoxville

23. Heo, Jinho. Analysis of polymorphism in human cytomegalovirus (HCMV) chemokine, vCXCL-1, and its role in cellular activation.

Degree: 2010, University of Tennessee – Knoxville

 The human cytomegalovirus (HCMV) viral chemokine gene, UL146, shows a high degree of variability in clinical isolates. The UL146-produced viral chemokine, vCXCL-1, has homology to… (more)

Subjects/Keywords: Cytomegalovirus; Chemokine; Polymorphism; Variability; Congenital; vCXCL-1; Virology

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APA (6th Edition):

Heo, J. (2010). Analysis of polymorphism in human cytomegalovirus (HCMV) chemokine, vCXCL-1, and its role in cellular activation. (Doctoral Dissertation). University of Tennessee – Knoxville. Retrieved from https://trace.tennessee.edu/utk_graddiss/885

Chicago Manual of Style (16th Edition):

Heo, Jinho. “Analysis of polymorphism in human cytomegalovirus (HCMV) chemokine, vCXCL-1, and its role in cellular activation.” 2010. Doctoral Dissertation, University of Tennessee – Knoxville. Accessed November 19, 2019. https://trace.tennessee.edu/utk_graddiss/885.

MLA Handbook (7th Edition):

Heo, Jinho. “Analysis of polymorphism in human cytomegalovirus (HCMV) chemokine, vCXCL-1, and its role in cellular activation.” 2010. Web. 19 Nov 2019.

Vancouver:

Heo J. Analysis of polymorphism in human cytomegalovirus (HCMV) chemokine, vCXCL-1, and its role in cellular activation. [Internet] [Doctoral dissertation]. University of Tennessee – Knoxville; 2010. [cited 2019 Nov 19]. Available from: https://trace.tennessee.edu/utk_graddiss/885.

Council of Science Editors:

Heo J. Analysis of polymorphism in human cytomegalovirus (HCMV) chemokine, vCXCL-1, and its role in cellular activation. [Doctoral Dissertation]. University of Tennessee – Knoxville; 2010. Available from: https://trace.tennessee.edu/utk_graddiss/885


University of Tennessee – Knoxville

24. Dogra, Pranay. CMV Chemokines and Co-infection: A Dissemination Plot that Peptides Can Foil.

Degree: 2015, University of Tennessee – Knoxville

 Human Cytomegalovirus (HCMV) is the leading cause of both non-hereditary mental retardation and hearing loss, and CMV infection/reactivation causes serious complications in transplant and immune… (more)

Subjects/Keywords: Cytomegalovirus; Chemokines; Co-infection; Viral Chemokines; Antiviral Peptides; Other Microbiology; Virology

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APA (6th Edition):

Dogra, P. (2015). CMV Chemokines and Co-infection: A Dissemination Plot that Peptides Can Foil. (Doctoral Dissertation). University of Tennessee – Knoxville. Retrieved from https://trace.tennessee.edu/utk_graddiss/3497

Chicago Manual of Style (16th Edition):

Dogra, Pranay. “CMV Chemokines and Co-infection: A Dissemination Plot that Peptides Can Foil.” 2015. Doctoral Dissertation, University of Tennessee – Knoxville. Accessed November 19, 2019. https://trace.tennessee.edu/utk_graddiss/3497.

MLA Handbook (7th Edition):

Dogra, Pranay. “CMV Chemokines and Co-infection: A Dissemination Plot that Peptides Can Foil.” 2015. Web. 19 Nov 2019.

Vancouver:

Dogra P. CMV Chemokines and Co-infection: A Dissemination Plot that Peptides Can Foil. [Internet] [Doctoral dissertation]. University of Tennessee – Knoxville; 2015. [cited 2019 Nov 19]. Available from: https://trace.tennessee.edu/utk_graddiss/3497.

Council of Science Editors:

Dogra P. CMV Chemokines and Co-infection: A Dissemination Plot that Peptides Can Foil. [Doctoral Dissertation]. University of Tennessee – Knoxville; 2015. Available from: https://trace.tennessee.edu/utk_graddiss/3497


Cornell University

25. Charles, Wisler. Cell-Intrinsic And Environmental Factors Altering The Neonatal Cd8+ T Cell Response To Mcmv In The Brain .

Degree: 2016, Cornell University

Subjects/Keywords: Cytomegalovirus; CD8+ T cells; Brain

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APA (6th Edition):

Charles, W. (2016). Cell-Intrinsic And Environmental Factors Altering The Neonatal Cd8+ T Cell Response To Mcmv In The Brain . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/45383

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):

Charles, Wisler. “Cell-Intrinsic And Environmental Factors Altering The Neonatal Cd8+ T Cell Response To Mcmv In The Brain .” 2016. Thesis, Cornell University. Accessed November 19, 2019. http://hdl.handle.net/1813/45383.

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

MLA Handbook (7th Edition):

Charles, Wisler. “Cell-Intrinsic And Environmental Factors Altering The Neonatal Cd8+ T Cell Response To Mcmv In The Brain .” 2016. Web. 19 Nov 2019.

Vancouver:

Charles W. Cell-Intrinsic And Environmental Factors Altering The Neonatal Cd8+ T Cell Response To Mcmv In The Brain . [Internet] [Thesis]. Cornell University; 2016. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/1813/45383.

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

Council of Science Editors:

Charles W. Cell-Intrinsic And Environmental Factors Altering The Neonatal Cd8+ T Cell Response To Mcmv In The Brain . [Thesis]. Cornell University; 2016. Available from: http://hdl.handle.net/1813/45383

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


University of Tennessee – Knoxville

26. Pitt, Elisabeth Anne. Chemokines and peptides that promote and inhibit CMV entry.

Degree: MS, Microbiology, 2016, University of Tennessee – Knoxville

  Human cytomegalovirus (HCMV) causes morbidity and mortality in congenitally infected newborns, transplant recipients, and AIDS patients. Currently, there is no approved CMV vaccine to… (more)

Subjects/Keywords: Cytomegalovirus; peptides; chemokines; pathogenesis; viral entry; Microbiology; Other Microbiology; Virology

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APA (6th Edition):

Pitt, E. A. (2016). Chemokines and peptides that promote and inhibit CMV entry. (Thesis). University of Tennessee – Knoxville. Retrieved from https://trace.tennessee.edu/utk_gradthes/4015

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):

Pitt, Elisabeth Anne. “Chemokines and peptides that promote and inhibit CMV entry.” 2016. Thesis, University of Tennessee – Knoxville. Accessed November 19, 2019. https://trace.tennessee.edu/utk_gradthes/4015.

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

MLA Handbook (7th Edition):

Pitt, Elisabeth Anne. “Chemokines and peptides that promote and inhibit CMV entry.” 2016. Web. 19 Nov 2019.

Vancouver:

Pitt EA. Chemokines and peptides that promote and inhibit CMV entry. [Internet] [Thesis]. University of Tennessee – Knoxville; 2016. [cited 2019 Nov 19]. Available from: https://trace.tennessee.edu/utk_gradthes/4015.

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

Council of Science Editors:

Pitt EA. Chemokines and peptides that promote and inhibit CMV entry. [Thesis]. University of Tennessee – Knoxville; 2016. Available from: https://trace.tennessee.edu/utk_gradthes/4015

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


Wayne State University

27. Close, William Longeway. Navigating Human Cytomegalovirus (hcmv) Envelopment And Egress.

Degree: PhD, Immunology and Microbiology, 2017, Wayne State University

  Human cytomegalovirus (HCMV) is a ubiquitous viral pathogen. In individuals with fully functioning and mature immune systems, HCMV is associated with mild symptoms prior… (more)

Subjects/Keywords: cytomegalovirus; egress; envelopment; herpesvirus; TB40/E/Cre; Biology; Molecular Biology; Virology

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APA (6th Edition):

Close, W. L. (2017). Navigating Human Cytomegalovirus (hcmv) Envelopment And Egress. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/1793

Chicago Manual of Style (16th Edition):

Close, William Longeway. “Navigating Human Cytomegalovirus (hcmv) Envelopment And Egress.” 2017. Doctoral Dissertation, Wayne State University. Accessed November 19, 2019. https://digitalcommons.wayne.edu/oa_dissertations/1793.

MLA Handbook (7th Edition):

Close, William Longeway. “Navigating Human Cytomegalovirus (hcmv) Envelopment And Egress.” 2017. Web. 19 Nov 2019.

Vancouver:

Close WL. Navigating Human Cytomegalovirus (hcmv) Envelopment And Egress. [Internet] [Doctoral dissertation]. Wayne State University; 2017. [cited 2019 Nov 19]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1793.

Council of Science Editors:

Close WL. Navigating Human Cytomegalovirus (hcmv) Envelopment And Egress. [Doctoral Dissertation]. Wayne State University; 2017. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1793


Wayne State University

28. Gurczynski, Stephen James. Human Cytomegalovirus Us17 Locus Fine-Tunes Innate And Intrinsic Immune Responses.

Degree: PhD, Immunology and Microbiology, 2013, Wayne State University

  HCMV employs numerous strategies to combat, subvert, or co-opt host immunity. One evolutionary strategy for this involves "capture" of a host gene and then… (more)

Subjects/Keywords: gene expression; human cytomegalovirus; innate immunity; Interferon; Microarray; US17; Microbiology; Virology

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APA (6th Edition):

Gurczynski, S. J. (2013). Human Cytomegalovirus Us17 Locus Fine-Tunes Innate And Intrinsic Immune Responses. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/840

Chicago Manual of Style (16th Edition):

Gurczynski, Stephen James. “Human Cytomegalovirus Us17 Locus Fine-Tunes Innate And Intrinsic Immune Responses.” 2013. Doctoral Dissertation, Wayne State University. Accessed November 19, 2019. https://digitalcommons.wayne.edu/oa_dissertations/840.

MLA Handbook (7th Edition):

Gurczynski, Stephen James. “Human Cytomegalovirus Us17 Locus Fine-Tunes Innate And Intrinsic Immune Responses.” 2013. Web. 19 Nov 2019.

Vancouver:

Gurczynski SJ. Human Cytomegalovirus Us17 Locus Fine-Tunes Innate And Intrinsic Immune Responses. [Internet] [Doctoral dissertation]. Wayne State University; 2013. [cited 2019 Nov 19]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/840.

Council of Science Editors:

Gurczynski SJ. Human Cytomegalovirus Us17 Locus Fine-Tunes Innate And Intrinsic Immune Responses. [Doctoral Dissertation]. Wayne State University; 2013. Available from: https://digitalcommons.wayne.edu/oa_dissertations/840


University of Arizona

29. Caviness, Katie Elizabeth. Complex Gene Expression And Interplay Of The UL136 Protein Isoforms Influence Human Cytomegalovirus Persistence .

Degree: 2015, University of Arizona

 Human cytomegalovirus (HCMV), a beta herpesvirus, persists indefinitely in the human host through a life-long, latent infection. HCMV is associated with life threatening pathologies in… (more)

Subjects/Keywords: Gene Expression; Herpesvirus; Isoforms; Latency; Persistence; Genetics; Cytomegalovirus

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

APA (6th Edition):

Caviness, K. E. (2015). Complex Gene Expression And Interplay Of The UL136 Protein Isoforms Influence Human Cytomegalovirus Persistence . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/556472

Chicago Manual of Style (16th Edition):

Caviness, Katie Elizabeth. “Complex Gene Expression And Interplay Of The UL136 Protein Isoforms Influence Human Cytomegalovirus Persistence .” 2015. Doctoral Dissertation, University of Arizona. Accessed November 19, 2019. http://hdl.handle.net/10150/556472.

MLA Handbook (7th Edition):

Caviness, Katie Elizabeth. “Complex Gene Expression And Interplay Of The UL136 Protein Isoforms Influence Human Cytomegalovirus Persistence .” 2015. Web. 19 Nov 2019.

Vancouver:

Caviness KE. Complex Gene Expression And Interplay Of The UL136 Protein Isoforms Influence Human Cytomegalovirus Persistence . [Internet] [Doctoral dissertation]. University of Arizona; 2015. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/10150/556472.

Council of Science Editors:

Caviness KE. Complex Gene Expression And Interplay Of The UL136 Protein Isoforms Influence Human Cytomegalovirus Persistence . [Doctoral Dissertation]. University of Arizona; 2015. Available from: http://hdl.handle.net/10150/556472


University of Arizona

30. Grainger, Lora Ann. Characterization of the Transcripts that Encode pUL138, a Latency Determinant, During Human Cytomegalovirus Infection .

Degree: 2010, University of Arizona

 Mechanisms involved in the establishment of HCMV latency are poorly understood, however, work in our laboratory has demonstrated the ULb' encoded protein, pUL138, as the… (more)

Subjects/Keywords: Human Cytomegalovirus; IRES; Latency; pUL138; Translation Initiation; Type I IFN

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

APA (6th Edition):

Grainger, L. A. (2010). Characterization of the Transcripts that Encode pUL138, a Latency Determinant, During Human Cytomegalovirus Infection . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/195915

Chicago Manual of Style (16th Edition):

Grainger, Lora Ann. “Characterization of the Transcripts that Encode pUL138, a Latency Determinant, During Human Cytomegalovirus Infection .” 2010. Doctoral Dissertation, University of Arizona. Accessed November 19, 2019. http://hdl.handle.net/10150/195915.

MLA Handbook (7th Edition):

Grainger, Lora Ann. “Characterization of the Transcripts that Encode pUL138, a Latency Determinant, During Human Cytomegalovirus Infection .” 2010. Web. 19 Nov 2019.

Vancouver:

Grainger LA. Characterization of the Transcripts that Encode pUL138, a Latency Determinant, During Human Cytomegalovirus Infection . [Internet] [Doctoral dissertation]. University of Arizona; 2010. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/10150/195915.

Council of Science Editors:

Grainger LA. Characterization of the Transcripts that Encode pUL138, a Latency Determinant, During Human Cytomegalovirus Infection . [Doctoral Dissertation]. University of Arizona; 2010. Available from: http://hdl.handle.net/10150/195915

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