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You searched for subject:(HSV 1). Showing records 1 – 30 of 116 total matches.

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University of Alberta

1. Rose, Alexandra R. A tale of two hypotheses: Effect of the herpes simplex-1 virus virion host shutoff (vhs) protein on bicistronic reporters.

Degree: MS, Department of Medical Microbiology and Immunology, 2014, University of Alberta

 The herpes simplex virus virion host shutoff (vhs) protein acts as an mRNA specific endoribonuclease. Our lab has previously determined that vhs stimulates expression of… (more)

Subjects/Keywords: HSV-1, vhs

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APA (6th Edition):

Rose, A. R. (2014). A tale of two hypotheses: Effect of the herpes simplex-1 virus virion host shutoff (vhs) protein on bicistronic reporters. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/xd07gw81q

Chicago Manual of Style (16th Edition):

Rose, Alexandra R. “A tale of two hypotheses: Effect of the herpes simplex-1 virus virion host shutoff (vhs) protein on bicistronic reporters.” 2014. Masters Thesis, University of Alberta. Accessed March 29, 2020. https://era.library.ualberta.ca/files/xd07gw81q.

MLA Handbook (7th Edition):

Rose, Alexandra R. “A tale of two hypotheses: Effect of the herpes simplex-1 virus virion host shutoff (vhs) protein on bicistronic reporters.” 2014. Web. 29 Mar 2020.

Vancouver:

Rose AR. A tale of two hypotheses: Effect of the herpes simplex-1 virus virion host shutoff (vhs) protein on bicistronic reporters. [Internet] [Masters thesis]. University of Alberta; 2014. [cited 2020 Mar 29]. Available from: https://era.library.ualberta.ca/files/xd07gw81q.

Council of Science Editors:

Rose AR. A tale of two hypotheses: Effect of the herpes simplex-1 virus virion host shutoff (vhs) protein on bicistronic reporters. [Masters Thesis]. University of Alberta; 2014. Available from: https://era.library.ualberta.ca/files/xd07gw81q

2. Delos, Maxime. Étude de la régulation d’expression et des activités des héparanes 3-O-sulfotransférases 2, 3A et 3B dans les macrophages : Study of the regulation of the expression and activities of heparan 3-O-sulfotransferases 2, 3A and 3B in macrophages.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2016, Université Lille I – Sciences et Technologies

Les héparanes sulfates (HS) sont des polysaccharides sulfatés qui participent à de nombreux processus physiopathologiques. L’entrée du virus HSV-1 dans ses cellules cibles nécessite l’intervention… (more)

Subjects/Keywords: HSV-1; 572.566

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APA (6th Edition):

Delos, M. (2016). Étude de la régulation d’expression et des activités des héparanes 3-O-sulfotransférases 2, 3A et 3B dans les macrophages : Study of the regulation of the expression and activities of heparan 3-O-sulfotransferases 2, 3A and 3B in macrophages. (Doctoral Dissertation). Université Lille I – Sciences et Technologies. Retrieved from http://www.theses.fr/2016LIL10162

Chicago Manual of Style (16th Edition):

Delos, Maxime. “Étude de la régulation d’expression et des activités des héparanes 3-O-sulfotransférases 2, 3A et 3B dans les macrophages : Study of the regulation of the expression and activities of heparan 3-O-sulfotransferases 2, 3A and 3B in macrophages.” 2016. Doctoral Dissertation, Université Lille I – Sciences et Technologies. Accessed March 29, 2020. http://www.theses.fr/2016LIL10162.

MLA Handbook (7th Edition):

Delos, Maxime. “Étude de la régulation d’expression et des activités des héparanes 3-O-sulfotransférases 2, 3A et 3B dans les macrophages : Study of the regulation of the expression and activities of heparan 3-O-sulfotransferases 2, 3A and 3B in macrophages.” 2016. Web. 29 Mar 2020.

Vancouver:

Delos M. Étude de la régulation d’expression et des activités des héparanes 3-O-sulfotransférases 2, 3A et 3B dans les macrophages : Study of the regulation of the expression and activities of heparan 3-O-sulfotransferases 2, 3A and 3B in macrophages. [Internet] [Doctoral dissertation]. Université Lille I – Sciences et Technologies; 2016. [cited 2020 Mar 29]. Available from: http://www.theses.fr/2016LIL10162.

Council of Science Editors:

Delos M. Étude de la régulation d’expression et des activités des héparanes 3-O-sulfotransférases 2, 3A et 3B dans les macrophages : Study of the regulation of the expression and activities of heparan 3-O-sulfotransferases 2, 3A and 3B in macrophages. [Doctoral Dissertation]. Université Lille I – Sciences et Technologies; 2016. Available from: http://www.theses.fr/2016LIL10162


UCLA

3. Chapon, Maxime. Optimizing innate immune signals to enhance antigen-specific adaptive responses.

Degree: Microbiology, Immunology, & Molecular Genetics, 2018, UCLA

 The innate and adaptive immune responses are intertwined systems that require complex regulation to achieve an efficient protection from pathogens and diseases. Upon sensing of… (more)

Subjects/Keywords: Immunology; Virology; HSV-1; Type 1 interferons

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APA (6th Edition):

Chapon, M. (2018). Optimizing innate immune signals to enhance antigen-specific adaptive responses. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/22s1f10b

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):

Chapon, Maxime. “Optimizing innate immune signals to enhance antigen-specific adaptive responses.” 2018. Thesis, UCLA. Accessed March 29, 2020. http://www.escholarship.org/uc/item/22s1f10b.

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

MLA Handbook (7th Edition):

Chapon, Maxime. “Optimizing innate immune signals to enhance antigen-specific adaptive responses.” 2018. Web. 29 Mar 2020.

Vancouver:

Chapon M. Optimizing innate immune signals to enhance antigen-specific adaptive responses. [Internet] [Thesis]. UCLA; 2018. [cited 2020 Mar 29]. Available from: http://www.escholarship.org/uc/item/22s1f10b.

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

Council of Science Editors:

Chapon M. Optimizing innate immune signals to enhance antigen-specific adaptive responses. [Thesis]. UCLA; 2018. Available from: http://www.escholarship.org/uc/item/22s1f10b

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


University of Manchester

4. Al-Sulaiman, Abdulrahman. Serological array for the diagnosis of viral infection of the central nervous system.

Degree: PhD, 2010, University of Manchester

 Encephalitis caused by the alphaherpes viruses HSV 1, HSV 2 and VZV can be devastating and rapid, accurate diagnosis is required. Whilst existing molecular techniques… (more)

Subjects/Keywords: 616.9; HSV-1; HSV-2; VZV; Encephalitis; Luminex technology

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APA (6th Edition):

Al-Sulaiman, A. (2010). Serological array for the diagnosis of viral infection of the central nervous system. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/serological-array-for-the-diagnosis-of-viral-infection-of-the-central-nervous-system(5c23bcf7-0679-437a-9617-342fc53e96d7).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.529236

Chicago Manual of Style (16th Edition):

Al-Sulaiman, Abdulrahman. “Serological array for the diagnosis of viral infection of the central nervous system.” 2010. Doctoral Dissertation, University of Manchester. Accessed March 29, 2020. https://www.research.manchester.ac.uk/portal/en/theses/serological-array-for-the-diagnosis-of-viral-infection-of-the-central-nervous-system(5c23bcf7-0679-437a-9617-342fc53e96d7).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.529236.

MLA Handbook (7th Edition):

Al-Sulaiman, Abdulrahman. “Serological array for the diagnosis of viral infection of the central nervous system.” 2010. Web. 29 Mar 2020.

Vancouver:

Al-Sulaiman A. Serological array for the diagnosis of viral infection of the central nervous system. [Internet] [Doctoral dissertation]. University of Manchester; 2010. [cited 2020 Mar 29]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/serological-array-for-the-diagnosis-of-viral-infection-of-the-central-nervous-system(5c23bcf7-0679-437a-9617-342fc53e96d7).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.529236.

Council of Science Editors:

Al-Sulaiman A. Serological array for the diagnosis of viral infection of the central nervous system. [Doctoral Dissertation]. University of Manchester; 2010. Available from: https://www.research.manchester.ac.uk/portal/en/theses/serological-array-for-the-diagnosis-of-viral-infection-of-the-central-nervous-system(5c23bcf7-0679-437a-9617-342fc53e96d7).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.529236


University of Alberta

5. Hancock, Meaghan. The roles of HSV-1 VP16 and ICP0 in modulating cellular innate antiviral responses.

Degree: PhD, Department of Medical Microbiology and Immunology, 2009, University of Alberta

 Infection of most cell types with herpes simplex virus (HSV) mutants lacking the activation functions of VP16 and/or ICP0 results in repression of viral gene… (more)

Subjects/Keywords: p14; ICP0; U2OS; HSV-1; VP16

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APA (6th Edition):

Hancock, M. (2009). The roles of HSV-1 VP16 and ICP0 in modulating cellular innate antiviral responses. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/bv73c089h

Chicago Manual of Style (16th Edition):

Hancock, Meaghan. “The roles of HSV-1 VP16 and ICP0 in modulating cellular innate antiviral responses.” 2009. Doctoral Dissertation, University of Alberta. Accessed March 29, 2020. https://era.library.ualberta.ca/files/bv73c089h.

MLA Handbook (7th Edition):

Hancock, Meaghan. “The roles of HSV-1 VP16 and ICP0 in modulating cellular innate antiviral responses.” 2009. Web. 29 Mar 2020.

Vancouver:

Hancock M. The roles of HSV-1 VP16 and ICP0 in modulating cellular innate antiviral responses. [Internet] [Doctoral dissertation]. University of Alberta; 2009. [cited 2020 Mar 29]. Available from: https://era.library.ualberta.ca/files/bv73c089h.

Council of Science Editors:

Hancock M. The roles of HSV-1 VP16 and ICP0 in modulating cellular innate antiviral responses. [Doctoral Dissertation]. University of Alberta; 2009. Available from: https://era.library.ualberta.ca/files/bv73c089h


University of Cincinnati

6. Maldonado, Arturo R. Molecular Targeting and Enhancing Anticancer Efficacy of Oncolytic HSV-1 to Midkine Expressing Tumors.

Degree: PhD, Medicine: Developmental Biology, 2011, University of Cincinnati

  Since 1999, cancer has surpassed heart disease as the number one cause of death in the US for people under the age of 85.… (more)

Subjects/Keywords: Molecular Biology; oncolytic; HSV-1; midkine; cancer

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APA (6th Edition):

Maldonado, A. R. (2011). Molecular Targeting and Enhancing Anticancer Efficacy of Oncolytic HSV-1 to Midkine Expressing Tumors. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1298041800

Chicago Manual of Style (16th Edition):

Maldonado, Arturo R. “Molecular Targeting and Enhancing Anticancer Efficacy of Oncolytic HSV-1 to Midkine Expressing Tumors.” 2011. Doctoral Dissertation, University of Cincinnati. Accessed March 29, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1298041800.

MLA Handbook (7th Edition):

Maldonado, Arturo R. “Molecular Targeting and Enhancing Anticancer Efficacy of Oncolytic HSV-1 to Midkine Expressing Tumors.” 2011. Web. 29 Mar 2020.

Vancouver:

Maldonado AR. Molecular Targeting and Enhancing Anticancer Efficacy of Oncolytic HSV-1 to Midkine Expressing Tumors. [Internet] [Doctoral dissertation]. University of Cincinnati; 2011. [cited 2020 Mar 29]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1298041800.

Council of Science Editors:

Maldonado AR. Molecular Targeting and Enhancing Anticancer Efficacy of Oncolytic HSV-1 to Midkine Expressing Tumors. [Doctoral Dissertation]. University of Cincinnati; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1298041800


The Ohio State University

7. Wu, Zetang. Silencing Suppression by Herpes Simplex Virus Type 1.

Degree: PhD, Molecular, Cellular, and Developmental Biology, 2008, The Ohio State University

 It was hypothesized that herpes simplex virus type-1 (HSV-1) encodes one or more silencing suppressors during productive infection. A transient silencing system was developed that… (more)

Subjects/Keywords: Virology; HSV-1; RNA silencing; silencing suppression

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APA (6th Edition):

Wu, Z. (2008). Silencing Suppression by Herpes Simplex Virus Type 1. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1213287215

Chicago Manual of Style (16th Edition):

Wu, Zetang. “Silencing Suppression by Herpes Simplex Virus Type 1.” 2008. Doctoral Dissertation, The Ohio State University. Accessed March 29, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1213287215.

MLA Handbook (7th Edition):

Wu, Zetang. “Silencing Suppression by Herpes Simplex Virus Type 1.” 2008. Web. 29 Mar 2020.

Vancouver:

Wu Z. Silencing Suppression by Herpes Simplex Virus Type 1. [Internet] [Doctoral dissertation]. The Ohio State University; 2008. [cited 2020 Mar 29]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1213287215.

Council of Science Editors:

Wu Z. Silencing Suppression by Herpes Simplex Virus Type 1. [Doctoral Dissertation]. The Ohio State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1213287215


Wright State University

8. Alamri, Badrieah Mohammad. Effects of Myrrh on HSV-1 Using Plaque Assay.

Degree: MS, Microbiology and Immunology, 2017, Wright State University

 Herpes simplex virus type 1 (HSV-1) is a highly infective human pathogen which infects a wide range of population in North America and worldwide. HSV-1(more)

Subjects/Keywords: Immunology; Myrrh; HSV-1; Vero cells

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APA (6th Edition):

Alamri, B. M. (2017). Effects of Myrrh on HSV-1 Using Plaque Assay. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1481628828816542

Chicago Manual of Style (16th Edition):

Alamri, Badrieah Mohammad. “Effects of Myrrh on HSV-1 Using Plaque Assay.” 2017. Masters Thesis, Wright State University. Accessed March 29, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=wright1481628828816542.

MLA Handbook (7th Edition):

Alamri, Badrieah Mohammad. “Effects of Myrrh on HSV-1 Using Plaque Assay.” 2017. Web. 29 Mar 2020.

Vancouver:

Alamri BM. Effects of Myrrh on HSV-1 Using Plaque Assay. [Internet] [Masters thesis]. Wright State University; 2017. [cited 2020 Mar 29]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1481628828816542.

Council of Science Editors:

Alamri BM. Effects of Myrrh on HSV-1 Using Plaque Assay. [Masters Thesis]. Wright State University; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1481628828816542


Wright State University

9. Alanazi, Yousef Nifaj. HSV-1 Replication in different RAW 264.7 and J774.1 macrophage Phenotypes and Macrophage viability following HSV-1 infection.

Degree: MS, Microbiology and Immunology, 2018, Wright State University

HSV-1 is a ubiquitous virus capable of causing lifelong latent infection. The virus contains a large double strand DNA genome covered by an icosahedral capsid.… (more)

Subjects/Keywords: Immunology; Microbiology; HSV-1; phenotype; macrophage

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APA (6th Edition):

Alanazi, Y. N. (2018). HSV-1 Replication in different RAW 264.7 and J774.1 macrophage Phenotypes and Macrophage viability following HSV-1 infection. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1525211483024617

Chicago Manual of Style (16th Edition):

Alanazi, Yousef Nifaj. “HSV-1 Replication in different RAW 264.7 and J774.1 macrophage Phenotypes and Macrophage viability following HSV-1 infection.” 2018. Masters Thesis, Wright State University. Accessed March 29, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=wright1525211483024617.

MLA Handbook (7th Edition):

Alanazi, Yousef Nifaj. “HSV-1 Replication in different RAW 264.7 and J774.1 macrophage Phenotypes and Macrophage viability following HSV-1 infection.” 2018. Web. 29 Mar 2020.

Vancouver:

Alanazi YN. HSV-1 Replication in different RAW 264.7 and J774.1 macrophage Phenotypes and Macrophage viability following HSV-1 infection. [Internet] [Masters thesis]. Wright State University; 2018. [cited 2020 Mar 29]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1525211483024617.

Council of Science Editors:

Alanazi YN. HSV-1 Replication in different RAW 264.7 and J774.1 macrophage Phenotypes and Macrophage viability following HSV-1 infection. [Masters Thesis]. Wright State University; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1525211483024617


Princeton University

10. Rowles, Daniell Lynn. SPATIAL-TEMPORAL VIRUS-HOST INTERACTIONS OF THE CAPSID PROTEIN VP26 DURING HSV-1 INFECTION.

Degree: PhD, 2013, Princeton University

 Herpes simplex virus type 1 (HSV-1) is an infectious pathogen imposing a substantial societal burden, while also having therapeutic potential. Throughout the course of infection,… (more)

Subjects/Keywords: DNMT3A; HSV-1; mass spectrometry; proteomics; VP26

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APA (6th Edition):

Rowles, D. L. (2013). SPATIAL-TEMPORAL VIRUS-HOST INTERACTIONS OF THE CAPSID PROTEIN VP26 DURING HSV-1 INFECTION. (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp019p290946b

Chicago Manual of Style (16th Edition):

Rowles, Daniell Lynn. “SPATIAL-TEMPORAL VIRUS-HOST INTERACTIONS OF THE CAPSID PROTEIN VP26 DURING HSV-1 INFECTION. ” 2013. Doctoral Dissertation, Princeton University. Accessed March 29, 2020. http://arks.princeton.edu/ark:/88435/dsp019p290946b.

MLA Handbook (7th Edition):

Rowles, Daniell Lynn. “SPATIAL-TEMPORAL VIRUS-HOST INTERACTIONS OF THE CAPSID PROTEIN VP26 DURING HSV-1 INFECTION. ” 2013. Web. 29 Mar 2020.

Vancouver:

Rowles DL. SPATIAL-TEMPORAL VIRUS-HOST INTERACTIONS OF THE CAPSID PROTEIN VP26 DURING HSV-1 INFECTION. [Internet] [Doctoral dissertation]. Princeton University; 2013. [cited 2020 Mar 29]. Available from: http://arks.princeton.edu/ark:/88435/dsp019p290946b.

Council of Science Editors:

Rowles DL. SPATIAL-TEMPORAL VIRUS-HOST INTERACTIONS OF THE CAPSID PROTEIN VP26 DURING HSV-1 INFECTION. [Doctoral Dissertation]. Princeton University; 2013. Available from: http://arks.princeton.edu/ark:/88435/dsp019p290946b


Louisiana State University

11. Musarrat, Farhana. Cellular and Viral Determinants of HSV-1 Entry and Transport.

Degree: PhD, Virology, 2019, Louisiana State University

  Previously, it was shown that the deletion of 38 amino acids from the N terminal end of glycoprotein K (gK) prevents the Herpes Simplex… (more)

Subjects/Keywords: HSV-1; entry; transport; gK; fusion; signaling

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APA (6th Edition):

Musarrat, F. (2019). Cellular and Viral Determinants of HSV-1 Entry and Transport. (Doctoral Dissertation). Louisiana State University. Retrieved from https://digitalcommons.lsu.edu/gradschool_dissertations/5084

Chicago Manual of Style (16th Edition):

Musarrat, Farhana. “Cellular and Viral Determinants of HSV-1 Entry and Transport.” 2019. Doctoral Dissertation, Louisiana State University. Accessed March 29, 2020. https://digitalcommons.lsu.edu/gradschool_dissertations/5084.

MLA Handbook (7th Edition):

Musarrat, Farhana. “Cellular and Viral Determinants of HSV-1 Entry and Transport.” 2019. Web. 29 Mar 2020.

Vancouver:

Musarrat F. Cellular and Viral Determinants of HSV-1 Entry and Transport. [Internet] [Doctoral dissertation]. Louisiana State University; 2019. [cited 2020 Mar 29]. Available from: https://digitalcommons.lsu.edu/gradschool_dissertations/5084.

Council of Science Editors:

Musarrat F. Cellular and Viral Determinants of HSV-1 Entry and Transport. [Doctoral Dissertation]. Louisiana State University; 2019. Available from: https://digitalcommons.lsu.edu/gradschool_dissertations/5084

12. Silva, Jaqueline Raymondi. Interações neuro-imunes envolvidas na gênese da hipersensibilidade nociceptiva herpética e pós-herpética.

Degree: PhD, Imunologia Básica e Aplicada, 2014, University of São Paulo

Herpes Zoster é uma doença causada pela reativação do vírus Varicela Zoster nos gânglios sensoriais, caracterizada pelo desenvolvimento de lesões na pele e dor. Não… (more)

Subjects/Keywords: COX-2; COX-2; Dor; HSV-1; HSV-1; Leucócitos; Leukocytes; Pain; TNF-; TNF-

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APA (6th Edition):

Silva, J. R. (2014). Interações neuro-imunes envolvidas na gênese da hipersensibilidade nociceptiva herpética e pós-herpética. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/17/17147/tde-26112014-163011/ ;

Chicago Manual of Style (16th Edition):

Silva, Jaqueline Raymondi. “Interações neuro-imunes envolvidas na gênese da hipersensibilidade nociceptiva herpética e pós-herpética.” 2014. Doctoral Dissertation, University of São Paulo. Accessed March 29, 2020. http://www.teses.usp.br/teses/disponiveis/17/17147/tde-26112014-163011/ ;.

MLA Handbook (7th Edition):

Silva, Jaqueline Raymondi. “Interações neuro-imunes envolvidas na gênese da hipersensibilidade nociceptiva herpética e pós-herpética.” 2014. Web. 29 Mar 2020.

Vancouver:

Silva JR. Interações neuro-imunes envolvidas na gênese da hipersensibilidade nociceptiva herpética e pós-herpética. [Internet] [Doctoral dissertation]. University of São Paulo; 2014. [cited 2020 Mar 29]. Available from: http://www.teses.usp.br/teses/disponiveis/17/17147/tde-26112014-163011/ ;.

Council of Science Editors:

Silva JR. Interações neuro-imunes envolvidas na gênese da hipersensibilidade nociceptiva herpética e pós-herpética. [Doctoral Dissertation]. University of São Paulo; 2014. Available from: http://www.teses.usp.br/teses/disponiveis/17/17147/tde-26112014-163011/ ;

13. Sabra, Mirna. Caractérisation de la réponse à l’instabilité des centromères (iCDR) déclenchée par la protéine ICP0 du Virus Herpès Simplex de type 1 (HSV-1) : Characterization of the interphase Centromere Damage Response (iCDR) triggered by the ICP0 protein of Herpes Simplex Virus Type 1 (HSV-1).

Degree: Docteur es, Biologie, 2010, Université Claude Bernard – Lyon I

L’infection par le virus de l’herpès simplex de type 1 (HSV-1), un virus pathogène humain majeur, engendre la déstabilisation des centromères. Cette déstabilisation est induite… (more)

Subjects/Keywords: HSV-1; ICP0; SMN; Dot1L; ICDR; H3K79; HSV-1; ICP0; SMN; Dot1L; ICDR; H3K79; 571.6

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APA (6th Edition):

Sabra, M. (2010). Caractérisation de la réponse à l’instabilité des centromères (iCDR) déclenchée par la protéine ICP0 du Virus Herpès Simplex de type 1 (HSV-1) : Characterization of the interphase Centromere Damage Response (iCDR) triggered by the ICP0 protein of Herpes Simplex Virus Type 1 (HSV-1). (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2010LYO10022

Chicago Manual of Style (16th Edition):

Sabra, Mirna. “Caractérisation de la réponse à l’instabilité des centromères (iCDR) déclenchée par la protéine ICP0 du Virus Herpès Simplex de type 1 (HSV-1) : Characterization of the interphase Centromere Damage Response (iCDR) triggered by the ICP0 protein of Herpes Simplex Virus Type 1 (HSV-1).” 2010. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed March 29, 2020. http://www.theses.fr/2010LYO10022.

MLA Handbook (7th Edition):

Sabra, Mirna. “Caractérisation de la réponse à l’instabilité des centromères (iCDR) déclenchée par la protéine ICP0 du Virus Herpès Simplex de type 1 (HSV-1) : Characterization of the interphase Centromere Damage Response (iCDR) triggered by the ICP0 protein of Herpes Simplex Virus Type 1 (HSV-1).” 2010. Web. 29 Mar 2020.

Vancouver:

Sabra M. Caractérisation de la réponse à l’instabilité des centromères (iCDR) déclenchée par la protéine ICP0 du Virus Herpès Simplex de type 1 (HSV-1) : Characterization of the interphase Centromere Damage Response (iCDR) triggered by the ICP0 protein of Herpes Simplex Virus Type 1 (HSV-1). [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2010. [cited 2020 Mar 29]. Available from: http://www.theses.fr/2010LYO10022.

Council of Science Editors:

Sabra M. Caractérisation de la réponse à l’instabilité des centromères (iCDR) déclenchée par la protéine ICP0 du Virus Herpès Simplex de type 1 (HSV-1) : Characterization of the interphase Centromere Damage Response (iCDR) triggered by the ICP0 protein of Herpes Simplex Virus Type 1 (HSV-1). [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2010. Available from: http://www.theses.fr/2010LYO10022


Université Paris-Sud – Paris XI

14. Huot, Nicolas. Relation entre l’expression des LAT et du gène RL2 pendant la latence du virus HSV-1 : Relationship between the expression of LAT and RL2 gene during HSV-1 latency.

Degree: Docteur es, Microbiologie, 2012, Université Paris-Sud – Paris XI

Le virus de l’herpès simplex de type 1 (HSV1) établit une infection latente dans le système nerveux de l'homme, au cours de laquelle un type… (more)

Subjects/Keywords: HSV-1; Latence; Réactivation; LAT; RL2; HSV-1; Latency; Reactivation; LAT; RL2

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APA (6th Edition):

Huot, N. (2012). Relation entre l’expression des LAT et du gène RL2 pendant la latence du virus HSV-1 : Relationship between the expression of LAT and RL2 gene during HSV-1 latency. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2012PA114860

Chicago Manual of Style (16th Edition):

Huot, Nicolas. “Relation entre l’expression des LAT et du gène RL2 pendant la latence du virus HSV-1 : Relationship between the expression of LAT and RL2 gene during HSV-1 latency.” 2012. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed March 29, 2020. http://www.theses.fr/2012PA114860.

MLA Handbook (7th Edition):

Huot, Nicolas. “Relation entre l’expression des LAT et du gène RL2 pendant la latence du virus HSV-1 : Relationship between the expression of LAT and RL2 gene during HSV-1 latency.” 2012. Web. 29 Mar 2020.

Vancouver:

Huot N. Relation entre l’expression des LAT et du gène RL2 pendant la latence du virus HSV-1 : Relationship between the expression of LAT and RL2 gene during HSV-1 latency. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2012. [cited 2020 Mar 29]. Available from: http://www.theses.fr/2012PA114860.

Council of Science Editors:

Huot N. Relation entre l’expression des LAT et du gène RL2 pendant la latence du virus HSV-1 : Relationship between the expression of LAT and RL2 gene during HSV-1 latency. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2012. Available from: http://www.theses.fr/2012PA114860


Université Paris-Sud – Paris XI

15. Lussignol, Marion. Caractérisation d’une nouvelle fonction de la protéine Us11 dans l’échappement à l’autophagie par le virus Herpès Simplex de type 1 : Characterization of a novel function of Us11 protein in HSV-1 escape from autophagy.

Degree: Docteur es, Microbiologie, 2013, Université Paris-Sud – Paris XI

L’autophagie est un mécanisme vacuolaire de dégradation de matériel cytoplasmique permettant le maintien de l’homéostasie cellulaire, mais elle peut être également activée par de nombreux… (more)

Subjects/Keywords: Autophagie; HSV-1; Us11; PKR; ICP34.5; Beclin 1; Autophagy; HSV-1; Us11; PKR; ICP34.5; Beclin 1

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APA (6th Edition):

Lussignol, M. (2013). Caractérisation d’une nouvelle fonction de la protéine Us11 dans l’échappement à l’autophagie par le virus Herpès Simplex de type 1 : Characterization of a novel function of Us11 protein in HSV-1 escape from autophagy. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2013PA114807

Chicago Manual of Style (16th Edition):

Lussignol, Marion. “Caractérisation d’une nouvelle fonction de la protéine Us11 dans l’échappement à l’autophagie par le virus Herpès Simplex de type 1 : Characterization of a novel function of Us11 protein in HSV-1 escape from autophagy.” 2013. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed March 29, 2020. http://www.theses.fr/2013PA114807.

MLA Handbook (7th Edition):

Lussignol, Marion. “Caractérisation d’une nouvelle fonction de la protéine Us11 dans l’échappement à l’autophagie par le virus Herpès Simplex de type 1 : Characterization of a novel function of Us11 protein in HSV-1 escape from autophagy.” 2013. Web. 29 Mar 2020.

Vancouver:

Lussignol M. Caractérisation d’une nouvelle fonction de la protéine Us11 dans l’échappement à l’autophagie par le virus Herpès Simplex de type 1 : Characterization of a novel function of Us11 protein in HSV-1 escape from autophagy. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2013. [cited 2020 Mar 29]. Available from: http://www.theses.fr/2013PA114807.

Council of Science Editors:

Lussignol M. Caractérisation d’une nouvelle fonction de la protéine Us11 dans l’échappement à l’autophagie par le virus Herpès Simplex de type 1 : Characterization of a novel function of Us11 protein in HSV-1 escape from autophagy. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2013. Available from: http://www.theses.fr/2013PA114807


Wright State University

16. Alhazmi, Amani Mohammed. The Response of M0, M1, and M2 RAW246.7 Macrophage Cell Line to HSV-1 Infection in vitro.

Degree: MS, Microbiology and Immunology, 2019, Wright State University

 Herpes Simplex Virus Type 1 (HSV-1) infection occurs through the epithelial cells of the skin or mucous membranes. The beginning of the primary infection is… (more)

Subjects/Keywords: Immunology; Herpes Simplex Virus Type 1; HSV-1; HSV-1 infection; macrophage; macrophage recruitment; macrophage differentiation

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APA (6th Edition):

Alhazmi, A. M. (2019). The Response of M0, M1, and M2 RAW246.7 Macrophage Cell Line to HSV-1 Infection in vitro. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1557759403892368

Chicago Manual of Style (16th Edition):

Alhazmi, Amani Mohammed. “The Response of M0, M1, and M2 RAW246.7 Macrophage Cell Line to HSV-1 Infection in vitro.” 2019. Masters Thesis, Wright State University. Accessed March 29, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=wright1557759403892368.

MLA Handbook (7th Edition):

Alhazmi, Amani Mohammed. “The Response of M0, M1, and M2 RAW246.7 Macrophage Cell Line to HSV-1 Infection in vitro.” 2019. Web. 29 Mar 2020.

Vancouver:

Alhazmi AM. The Response of M0, M1, and M2 RAW246.7 Macrophage Cell Line to HSV-1 Infection in vitro. [Internet] [Masters thesis]. Wright State University; 2019. [cited 2020 Mar 29]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1557759403892368.

Council of Science Editors:

Alhazmi AM. The Response of M0, M1, and M2 RAW246.7 Macrophage Cell Line to HSV-1 Infection in vitro. [Masters Thesis]. Wright State University; 2019. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1557759403892368


Temple University

17. Milora, Katelynn Ann. Characterization of IL-1 and IL-36 Cytokines in Health and Disease.

Degree: PhD, 2017, Temple University

Microbiology and Immunology

Epithelial cells are the first line of defense against invading pathogens and external threats in the environment. Keratinocytes, often not perceived of… (more)

Subjects/Keywords: Immunology;

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APA (6th Edition):

Milora, K. A. (2017). Characterization of IL-1 and IL-36 Cytokines in Health and Disease. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,451599

Chicago Manual of Style (16th Edition):

Milora, Katelynn Ann. “Characterization of IL-1 and IL-36 Cytokines in Health and Disease.” 2017. Doctoral Dissertation, Temple University. Accessed March 29, 2020. http://digital.library.temple.edu/u?/p245801coll10,451599.

MLA Handbook (7th Edition):

Milora, Katelynn Ann. “Characterization of IL-1 and IL-36 Cytokines in Health and Disease.” 2017. Web. 29 Mar 2020.

Vancouver:

Milora KA. Characterization of IL-1 and IL-36 Cytokines in Health and Disease. [Internet] [Doctoral dissertation]. Temple University; 2017. [cited 2020 Mar 29]. Available from: http://digital.library.temple.edu/u?/p245801coll10,451599.

Council of Science Editors:

Milora KA. Characterization of IL-1 and IL-36 Cytokines in Health and Disease. [Doctoral Dissertation]. Temple University; 2017. Available from: http://digital.library.temple.edu/u?/p245801coll10,451599


Penn State University

18. O'Regan, Kevin Joseph. INSIGHTS INTO HERPES SIMPLEX VIRUS TYPE 1 ASSEMBLY: PROTEIN INTERACTIONS AND VIRION INCORPORATION DETERMINANTS OF THE TEGUMENT PROTEIN VP22.

Degree: PhD, Microbiology and Immunology, 2008, Penn State University

 Herpes simplex virus type 1 (HSV-1) assembly involves a complex sequence of events occurring within numerous cellular compartments that culminates in the formation of virions… (more)

Subjects/Keywords: Herpes simplex virus type 1: HSV-1: VP22: VP16: Gl

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APA (6th Edition):

O'Regan, K. J. (2008). INSIGHTS INTO HERPES SIMPLEX VIRUS TYPE 1 ASSEMBLY: PROTEIN INTERACTIONS AND VIRION INCORPORATION DETERMINANTS OF THE TEGUMENT PROTEIN VP22. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/8115

Chicago Manual of Style (16th Edition):

O'Regan, Kevin Joseph. “INSIGHTS INTO HERPES SIMPLEX VIRUS TYPE 1 ASSEMBLY: PROTEIN INTERACTIONS AND VIRION INCORPORATION DETERMINANTS OF THE TEGUMENT PROTEIN VP22.” 2008. Doctoral Dissertation, Penn State University. Accessed March 29, 2020. https://etda.libraries.psu.edu/catalog/8115.

MLA Handbook (7th Edition):

O'Regan, Kevin Joseph. “INSIGHTS INTO HERPES SIMPLEX VIRUS TYPE 1 ASSEMBLY: PROTEIN INTERACTIONS AND VIRION INCORPORATION DETERMINANTS OF THE TEGUMENT PROTEIN VP22.” 2008. Web. 29 Mar 2020.

Vancouver:

O'Regan KJ. INSIGHTS INTO HERPES SIMPLEX VIRUS TYPE 1 ASSEMBLY: PROTEIN INTERACTIONS AND VIRION INCORPORATION DETERMINANTS OF THE TEGUMENT PROTEIN VP22. [Internet] [Doctoral dissertation]. Penn State University; 2008. [cited 2020 Mar 29]. Available from: https://etda.libraries.psu.edu/catalog/8115.

Council of Science Editors:

O'Regan KJ. INSIGHTS INTO HERPES SIMPLEX VIRUS TYPE 1 ASSEMBLY: PROTEIN INTERACTIONS AND VIRION INCORPORATION DETERMINANTS OF THE TEGUMENT PROTEIN VP22. [Doctoral Dissertation]. Penn State University; 2008. Available from: https://etda.libraries.psu.edu/catalog/8115

19. Pourchet, Aldo Decio. Développement de virus HSV-1 (virus de l’herpes simplex de type 1) oncolytiques ciblés pour traiter les carcinomes hépatocellulaires : Oncolytic HSV-1 (herpes simplex virus type 1) transcriptionally targeted against hepatocellular carcinoma.

Degree: Docteur es, Virologie, 2010, Université Claude Bernard – Lyon I

Le premier objectif a été de sélectionner des promoteurs de gènes cellulaires actifs spécifiquement dans les HCC à l’aide d’une recherche bibliographique puis en utilisant… (more)

Subjects/Keywords: Virus oncolytiques; Ciblage transcriptionnel; HSV-1; Carcinome hépatocellulaire (HCC); Promoteur; Oncolytic viruses; Transcriptional targeting; HSV-1; Hepatocellular carcinoma (HCC); Promoter

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APA (6th Edition):

Pourchet, A. D. (2010). Développement de virus HSV-1 (virus de l’herpes simplex de type 1) oncolytiques ciblés pour traiter les carcinomes hépatocellulaires : Oncolytic HSV-1 (herpes simplex virus type 1) transcriptionally targeted against hepatocellular carcinoma. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2010LYO10155

Chicago Manual of Style (16th Edition):

Pourchet, Aldo Decio. “Développement de virus HSV-1 (virus de l’herpes simplex de type 1) oncolytiques ciblés pour traiter les carcinomes hépatocellulaires : Oncolytic HSV-1 (herpes simplex virus type 1) transcriptionally targeted against hepatocellular carcinoma.” 2010. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed March 29, 2020. http://www.theses.fr/2010LYO10155.

MLA Handbook (7th Edition):

Pourchet, Aldo Decio. “Développement de virus HSV-1 (virus de l’herpes simplex de type 1) oncolytiques ciblés pour traiter les carcinomes hépatocellulaires : Oncolytic HSV-1 (herpes simplex virus type 1) transcriptionally targeted against hepatocellular carcinoma.” 2010. Web. 29 Mar 2020.

Vancouver:

Pourchet AD. Développement de virus HSV-1 (virus de l’herpes simplex de type 1) oncolytiques ciblés pour traiter les carcinomes hépatocellulaires : Oncolytic HSV-1 (herpes simplex virus type 1) transcriptionally targeted against hepatocellular carcinoma. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2010. [cited 2020 Mar 29]. Available from: http://www.theses.fr/2010LYO10155.

Council of Science Editors:

Pourchet AD. Développement de virus HSV-1 (virus de l’herpes simplex de type 1) oncolytiques ciblés pour traiter les carcinomes hépatocellulaires : Oncolytic HSV-1 (herpes simplex virus type 1) transcriptionally targeted against hepatocellular carcinoma. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2010. Available from: http://www.theses.fr/2010LYO10155


Université de Montréal

20. Zhang, Jie. Contribution de la Glycoprotéine M dans la Sortie de HSV-1 .

Degree: 2010, Université de Montréal

 Le Virus Herpès Simplex de type 1 (HSV-1) est un agent infectieux qui cause l’herpès chez une grande proportion de la population mondiale. L’herpès est… (more)

Subjects/Keywords: Virus Herpès Simplex de type 1 (VHS-1 ou HSV-1); herpes simplex virus type 1 (HSV-1); glycoprotéine M (gM); glycoprotein gM (gM)

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APA (6th Edition):

Zhang, J. (2010). Contribution de la Glycoprotéine M dans la Sortie de HSV-1 . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/4545

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):

Zhang, Jie. “Contribution de la Glycoprotéine M dans la Sortie de HSV-1 .” 2010. Thesis, Université de Montréal. Accessed March 29, 2020. http://hdl.handle.net/1866/4545.

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

MLA Handbook (7th Edition):

Zhang, Jie. “Contribution de la Glycoprotéine M dans la Sortie de HSV-1 .” 2010. Web. 29 Mar 2020.

Vancouver:

Zhang J. Contribution de la Glycoprotéine M dans la Sortie de HSV-1 . [Internet] [Thesis]. Université de Montréal; 2010. [cited 2020 Mar 29]. Available from: http://hdl.handle.net/1866/4545.

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

Council of Science Editors:

Zhang J. Contribution de la Glycoprotéine M dans la Sortie de HSV-1 . [Thesis]. Université de Montréal; 2010. Available from: http://hdl.handle.net/1866/4545

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


University of Alberta

21. Quach, Kevin. HSV-1 Remodels PI3-Kinase/AKT Signaling.

Degree: MS, Department of Medical Microbiology and Immunology, 2013, University of Alberta

 AKT inhibits apoptosis and stimulates cap-dependent translation by phosphorylating key downstream cellular proteins. Many viruses therefore activate the PI3-kinase-AKT signaling pathway to promote cell survival… (more)

Subjects/Keywords: Herpes; AKT; Us3; PI3K; UL46; HSV-1; PDGF; VP11/12

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APA (6th Edition):

Quach, K. (2013). HSV-1 Remodels PI3-Kinase/AKT Signaling. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/pr76f4765

Chicago Manual of Style (16th Edition):

Quach, Kevin. “HSV-1 Remodels PI3-Kinase/AKT Signaling.” 2013. Masters Thesis, University of Alberta. Accessed March 29, 2020. https://era.library.ualberta.ca/files/pr76f4765.

MLA Handbook (7th Edition):

Quach, Kevin. “HSV-1 Remodels PI3-Kinase/AKT Signaling.” 2013. Web. 29 Mar 2020.

Vancouver:

Quach K. HSV-1 Remodels PI3-Kinase/AKT Signaling. [Internet] [Masters thesis]. University of Alberta; 2013. [cited 2020 Mar 29]. Available from: https://era.library.ualberta.ca/files/pr76f4765.

Council of Science Editors:

Quach K. HSV-1 Remodels PI3-Kinase/AKT Signaling. [Masters Thesis]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/pr76f4765


University of Rochester

22. Simon, David Adam Louis. Mechanisms of viral vector induced immune responses and analysis of a transgenic mouse prostate tumor model.

Degree: PhD, 2009, University of Rochester

 Effective tumor immunotherapy, despite impressive advances, remains an elusive goal. Better immunization strategies, as well as improved animal models to test therapeutic strategies, are critical… (more)

Subjects/Keywords: HSV-1 amplicons; Viral vectors; Tumor model; VLPs

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APA (6th Edition):

Simon, D. A. L. (2009). Mechanisms of viral vector induced immune responses and analysis of a transgenic mouse prostate tumor model. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/6544

Chicago Manual of Style (16th Edition):

Simon, David Adam Louis. “Mechanisms of viral vector induced immune responses and analysis of a transgenic mouse prostate tumor model.” 2009. Doctoral Dissertation, University of Rochester. Accessed March 29, 2020. http://hdl.handle.net/1802/6544.

MLA Handbook (7th Edition):

Simon, David Adam Louis. “Mechanisms of viral vector induced immune responses and analysis of a transgenic mouse prostate tumor model.” 2009. Web. 29 Mar 2020.

Vancouver:

Simon DAL. Mechanisms of viral vector induced immune responses and analysis of a transgenic mouse prostate tumor model. [Internet] [Doctoral dissertation]. University of Rochester; 2009. [cited 2020 Mar 29]. Available from: http://hdl.handle.net/1802/6544.

Council of Science Editors:

Simon DAL. Mechanisms of viral vector induced immune responses and analysis of a transgenic mouse prostate tumor model. [Doctoral Dissertation]. University of Rochester; 2009. Available from: http://hdl.handle.net/1802/6544


Wright State University

23. Abbas, Asma A. HSV-1 INFECTION IN KERATINOCYTE CELL LINES TREATED WITH MITOTIC INHIBITORS.

Degree: MS, Microbiology and Immunology, 2011, Wright State University

 The hypothesis for this research was: Herpes simplex virus type 1 (HSV-1) infection of murine keratinocyte cell lines (HEL-30 and PAM-212) treated with mitotic inhibitors… (more)

Subjects/Keywords: Immunology; HSV-1 infection; keratinocyte cell lines; mitotic inhibitors

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APA (6th Edition):

Abbas, A. A. (2011). HSV-1 INFECTION IN KERATINOCYTE CELL LINES TREATED WITH MITOTIC INHIBITORS. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1303839668

Chicago Manual of Style (16th Edition):

Abbas, Asma A. “HSV-1 INFECTION IN KERATINOCYTE CELL LINES TREATED WITH MITOTIC INHIBITORS.” 2011. Masters Thesis, Wright State University. Accessed March 29, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=wright1303839668.

MLA Handbook (7th Edition):

Abbas, Asma A. “HSV-1 INFECTION IN KERATINOCYTE CELL LINES TREATED WITH MITOTIC INHIBITORS.” 2011. Web. 29 Mar 2020.

Vancouver:

Abbas AA. HSV-1 INFECTION IN KERATINOCYTE CELL LINES TREATED WITH MITOTIC INHIBITORS. [Internet] [Masters thesis]. Wright State University; 2011. [cited 2020 Mar 29]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1303839668.

Council of Science Editors:

Abbas AA. HSV-1 INFECTION IN KERATINOCYTE CELL LINES TREATED WITH MITOTIC INHIBITORS. [Masters Thesis]. Wright State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1303839668


Wright State University

24. Aldreiwish, Allolo Dreiwish. The Effect of HSV-1 Infection on Differentiated and Polarized U937 cells.

Degree: MS, Microbiology and Immunology, 2013, Wright State University

 Herpes simplex virus type 1 (HSV-1) challenges the host immune systemthrough several mechanisms (Frey, et al., 2009). In vitro, U937 cells (humanmacrophage-like precursor cell line)… (more)

Subjects/Keywords: Immunology; Microbiology; U937; HSV-1; Macrophages polarization; Differentiation of U937

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APA (6th Edition):

Aldreiwish, A. D. (2013). The Effect of HSV-1 Infection on Differentiated and Polarized U937 cells. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1389610801

Chicago Manual of Style (16th Edition):

Aldreiwish, Allolo Dreiwish. “The Effect of HSV-1 Infection on Differentiated and Polarized U937 cells.” 2013. Masters Thesis, Wright State University. Accessed March 29, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=wright1389610801.

MLA Handbook (7th Edition):

Aldreiwish, Allolo Dreiwish. “The Effect of HSV-1 Infection on Differentiated and Polarized U937 cells.” 2013. Web. 29 Mar 2020.

Vancouver:

Aldreiwish AD. The Effect of HSV-1 Infection on Differentiated and Polarized U937 cells. [Internet] [Masters thesis]. Wright State University; 2013. [cited 2020 Mar 29]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1389610801.

Council of Science Editors:

Aldreiwish AD. The Effect of HSV-1 Infection on Differentiated and Polarized U937 cells. [Masters Thesis]. Wright State University; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1389610801


Louisiana State University

25. Lee, HyunCheol. Comparative roles of herpes simplex virus type 1 (HSV-1) glycoproteins in cytoplasmic virion egress.

Degree: MS, Veterinary Pathology and Pathobiology, 2008, Louisiana State University

HSV-1 acquires its final envelope by budding into cytoplasmic vesicles thought to be derived from Trans-Golgi Network (TGN) membranes. This process is facilitated by interactions… (more)

Subjects/Keywords: cytoplasmic envelopment; glycoproteins; HSV-1

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APA (6th Edition):

Lee, H. (2008). Comparative roles of herpes simplex virus type 1 (HSV-1) glycoproteins in cytoplasmic virion egress. (Masters Thesis). Louisiana State University. Retrieved from etd-07082008-083329 ; https://digitalcommons.lsu.edu/gradschool_theses/898

Chicago Manual of Style (16th Edition):

Lee, HyunCheol. “Comparative roles of herpes simplex virus type 1 (HSV-1) glycoproteins in cytoplasmic virion egress.” 2008. Masters Thesis, Louisiana State University. Accessed March 29, 2020. etd-07082008-083329 ; https://digitalcommons.lsu.edu/gradschool_theses/898.

MLA Handbook (7th Edition):

Lee, HyunCheol. “Comparative roles of herpes simplex virus type 1 (HSV-1) glycoproteins in cytoplasmic virion egress.” 2008. Web. 29 Mar 2020.

Vancouver:

Lee H. Comparative roles of herpes simplex virus type 1 (HSV-1) glycoproteins in cytoplasmic virion egress. [Internet] [Masters thesis]. Louisiana State University; 2008. [cited 2020 Mar 29]. Available from: etd-07082008-083329 ; https://digitalcommons.lsu.edu/gradschool_theses/898.

Council of Science Editors:

Lee H. Comparative roles of herpes simplex virus type 1 (HSV-1) glycoproteins in cytoplasmic virion egress. [Masters Thesis]. Louisiana State University; 2008. Available from: etd-07082008-083329 ; https://digitalcommons.lsu.edu/gradschool_theses/898


Louisiana State University

26. Saied, Ahmad. The Role of Herpes Simplex Virus Type 1 Glycoprotein K in Neuroinvasion and Immunopathogenesis of Herpes Keratitis.

Degree: PhD, Veterinary Pathology and Pathobiology, 2015, Louisiana State University

 ABSTRACT Herpes simplex virus type 1 is a common neurotropic pathogen responsible for a multitude of human diseases ranging from mucocutaneous lesions, keratitis to life-threatening… (more)

Subjects/Keywords: HSV-1; Glycoprotein K; Neuroinvasion; Immunopathogenesis; Herpes Keratitis

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

APA (6th Edition):

Saied, A. (2015). The Role of Herpes Simplex Virus Type 1 Glycoprotein K in Neuroinvasion and Immunopathogenesis of Herpes Keratitis. (Doctoral Dissertation). Louisiana State University. Retrieved from etd-04012015-164717 ; https://digitalcommons.lsu.edu/gradschool_dissertations/3640

Chicago Manual of Style (16th Edition):

Saied, Ahmad. “The Role of Herpes Simplex Virus Type 1 Glycoprotein K in Neuroinvasion and Immunopathogenesis of Herpes Keratitis.” 2015. Doctoral Dissertation, Louisiana State University. Accessed March 29, 2020. etd-04012015-164717 ; https://digitalcommons.lsu.edu/gradschool_dissertations/3640.

MLA Handbook (7th Edition):

Saied, Ahmad. “The Role of Herpes Simplex Virus Type 1 Glycoprotein K in Neuroinvasion and Immunopathogenesis of Herpes Keratitis.” 2015. Web. 29 Mar 2020.

Vancouver:

Saied A. The Role of Herpes Simplex Virus Type 1 Glycoprotein K in Neuroinvasion and Immunopathogenesis of Herpes Keratitis. [Internet] [Doctoral dissertation]. Louisiana State University; 2015. [cited 2020 Mar 29]. Available from: etd-04012015-164717 ; https://digitalcommons.lsu.edu/gradschool_dissertations/3640.

Council of Science Editors:

Saied A. The Role of Herpes Simplex Virus Type 1 Glycoprotein K in Neuroinvasion and Immunopathogenesis of Herpes Keratitis. [Doctoral Dissertation]. Louisiana State University; 2015. Available from: etd-04012015-164717 ; https://digitalcommons.lsu.edu/gradschool_dissertations/3640


University of Kansas

27. Fowler, Angela Marie. Identifying cellular kinases that regulate HSV-1 ICP0 activities and viral replication.

Degree: PhD, Molecular Biosciences, 2016, University of Kansas

 Herpes simplex virus 1 (HSV-1) infects a significant number of people worldwide and is the number one cause of infectious blindness in western industrialized countries.… (more)

Subjects/Keywords: Virology; Microbiology; CDKs; cellular kinases; HSV-1; ICP0; viral replication

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

APA (6th Edition):

Fowler, A. M. (2016). Identifying cellular kinases that regulate HSV-1 ICP0 activities and viral replication. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/25779

Chicago Manual of Style (16th Edition):

Fowler, Angela Marie. “Identifying cellular kinases that regulate HSV-1 ICP0 activities and viral replication.” 2016. Doctoral Dissertation, University of Kansas. Accessed March 29, 2020. http://hdl.handle.net/1808/25779.

MLA Handbook (7th Edition):

Fowler, Angela Marie. “Identifying cellular kinases that regulate HSV-1 ICP0 activities and viral replication.” 2016. Web. 29 Mar 2020.

Vancouver:

Fowler AM. Identifying cellular kinases that regulate HSV-1 ICP0 activities and viral replication. [Internet] [Doctoral dissertation]. University of Kansas; 2016. [cited 2020 Mar 29]. Available from: http://hdl.handle.net/1808/25779.

Council of Science Editors:

Fowler AM. Identifying cellular kinases that regulate HSV-1 ICP0 activities and viral replication. [Doctoral Dissertation]. University of Kansas; 2016. Available from: http://hdl.handle.net/1808/25779


Harvard University

28. Orzalli, Megan Horn. Inhibition of Nuclear DNA Sensing by Herpes Simplex Virus 1.

Degree: PhD, Biology: Medical Sciences, Division of, 2013, Harvard University

 The detection of immunostimulatory DNA is well documented to occur at several cellular sites, but there is limited evidence of nuclear innate DNA sensing. Prior… (more)

Subjects/Keywords: Virology; DNA sensing; HSV-1; ICP0; IFI16; intrinsic antiviral resistance; IRF3

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

APA (6th Edition):

Orzalli, M. H. (2013). Inhibition of Nuclear DNA Sensing by Herpes Simplex Virus 1. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:11156815

Chicago Manual of Style (16th Edition):

Orzalli, Megan Horn. “Inhibition of Nuclear DNA Sensing by Herpes Simplex Virus 1.” 2013. Doctoral Dissertation, Harvard University. Accessed March 29, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:11156815.

MLA Handbook (7th Edition):

Orzalli, Megan Horn. “Inhibition of Nuclear DNA Sensing by Herpes Simplex Virus 1.” 2013. Web. 29 Mar 2020.

Vancouver:

Orzalli MH. Inhibition of Nuclear DNA Sensing by Herpes Simplex Virus 1. [Internet] [Doctoral dissertation]. Harvard University; 2013. [cited 2020 Mar 29]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:11156815.

Council of Science Editors:

Orzalli MH. Inhibition of Nuclear DNA Sensing by Herpes Simplex Virus 1. [Doctoral Dissertation]. Harvard University; 2013. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:11156815

29. Van Opdenbosch, Nina. A triple entente? : interplay between alphaherpesviruses and interferon in sensory neuronal cells.

Degree: 2011, Ghent University

 Alfaherpesvirussen bezitten de gemeenschappelijke eigenschap om een levenslange latente, slapende infectie te veroorzaken, veelal in sensorische neuronen. Het wordt steeds duidelijker dat het gastheer immuunsysteem,… (more)

Subjects/Keywords: Veterinary Sciences; PRV; Immune system; Alphaherpesvirus; HSV-1; Interferon; Neuron

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

APA (6th Edition):

Van Opdenbosch, N. (2011). A triple entente? : interplay between alphaherpesviruses and interferon in sensory neuronal cells. (Thesis). Ghent University. Retrieved from http://hdl.handle.net/1854/LU-4234848

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):

Van Opdenbosch, Nina. “A triple entente? : interplay between alphaherpesviruses and interferon in sensory neuronal cells.” 2011. Thesis, Ghent University. Accessed March 29, 2020. http://hdl.handle.net/1854/LU-4234848.

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

MLA Handbook (7th Edition):

Van Opdenbosch, Nina. “A triple entente? : interplay between alphaherpesviruses and interferon in sensory neuronal cells.” 2011. Web. 29 Mar 2020.

Vancouver:

Van Opdenbosch N. A triple entente? : interplay between alphaherpesviruses and interferon in sensory neuronal cells. [Internet] [Thesis]. Ghent University; 2011. [cited 2020 Mar 29]. Available from: http://hdl.handle.net/1854/LU-4234848.

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

Council of Science Editors:

Van Opdenbosch N. A triple entente? : interplay between alphaherpesviruses and interferon in sensory neuronal cells. [Thesis]. Ghent University; 2011. Available from: http://hdl.handle.net/1854/LU-4234848

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


University of Texas – Austin

30. Lou, Dianne In-Hye. Strategies for deciphering the genome.

Degree: PhD, Cell and Molecular Biology, 2014, University of Texas – Austin

 The development of highly sophisticated technologies has ushered in the era of the genome. Most importantly, high-throughput sequencing technologies has vastly expanded the number of… (more)

Subjects/Keywords: DNA repair; Evolution; High-throughput sequencing; Primates; HSV-1; Viruses

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

APA (6th Edition):

Lou, D. I. (2014). Strategies for deciphering the genome. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/33259

Chicago Manual of Style (16th Edition):

Lou, Dianne In-Hye. “Strategies for deciphering the genome.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed March 29, 2020. http://hdl.handle.net/2152/33259.

MLA Handbook (7th Edition):

Lou, Dianne In-Hye. “Strategies for deciphering the genome.” 2014. Web. 29 Mar 2020.

Vancouver:

Lou DI. Strategies for deciphering the genome. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Mar 29]. Available from: http://hdl.handle.net/2152/33259.

Council of Science Editors:

Lou DI. Strategies for deciphering the genome. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/33259

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