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You searched for subject:(Virus Fusion). Showing records 1 – 30 of 77 total matches.

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Cornell University

1. Costello, Deirdre. Single Virion Fusion Studies Of Membrane-Enveloped Viruses To Biomimetic Membranes.

Degree: PhD, Chemical Engineering, 2014, Cornell University

 SINGLE VIRION FUSION STUDIES OF MEMBRANE-ENVELOPED VIRUSES TO CELL-DERIVED MEMBRANES Deirdre Ann Costello, Ph. D. Cornell University [2014] Understanding the mechanisms involved in the viral… (more)

Subjects/Keywords: Virus fusion; single virion; biomimetic membranes

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APA (6th Edition):

Costello, D. (2014). Single Virion Fusion Studies Of Membrane-Enveloped Viruses To Biomimetic Membranes. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/37041

Chicago Manual of Style (16th Edition):

Costello, Deirdre. “Single Virion Fusion Studies Of Membrane-Enveloped Viruses To Biomimetic Membranes.” 2014. Doctoral Dissertation, Cornell University. Accessed November 23, 2020. http://hdl.handle.net/1813/37041.

MLA Handbook (7th Edition):

Costello, Deirdre. “Single Virion Fusion Studies Of Membrane-Enveloped Viruses To Biomimetic Membranes.” 2014. Web. 23 Nov 2020.

Vancouver:

Costello D. Single Virion Fusion Studies Of Membrane-Enveloped Viruses To Biomimetic Membranes. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2020 Nov 23]. Available from: http://hdl.handle.net/1813/37041.

Council of Science Editors:

Costello D. Single Virion Fusion Studies Of Membrane-Enveloped Viruses To Biomimetic Membranes. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/37041


Louisiana State University

2. Kim, In Joong. Herpes simplex virus type 1 glycoprotein gM and the membrane associated protein UL11 are required for virus-induced cell fusion and efficient virus entry.

Degree: PhD, Veterinary Pathology and Pathobiology, 2013, Louisiana State University

  HSV-1 facilitates virus entry into cells and cell-to-cell spread by mediating fusion of the viral envelope with cellular membranes and fusion of adjacent cellular… (more)

Subjects/Keywords: Herpes simplex virus; glycoprotein; fusion; entry

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APA (6th Edition):

Kim, I. J. (2013). Herpes simplex virus type 1 glycoprotein gM and the membrane associated protein UL11 are required for virus-induced cell fusion and efficient virus entry. (Doctoral Dissertation). Louisiana State University. Retrieved from etd-11132013-135946 ; https://digitalcommons.lsu.edu/gradschool_dissertations/3897

Chicago Manual of Style (16th Edition):

Kim, In Joong. “Herpes simplex virus type 1 glycoprotein gM and the membrane associated protein UL11 are required for virus-induced cell fusion and efficient virus entry.” 2013. Doctoral Dissertation, Louisiana State University. Accessed November 23, 2020. etd-11132013-135946 ; https://digitalcommons.lsu.edu/gradschool_dissertations/3897.

MLA Handbook (7th Edition):

Kim, In Joong. “Herpes simplex virus type 1 glycoprotein gM and the membrane associated protein UL11 are required for virus-induced cell fusion and efficient virus entry.” 2013. Web. 23 Nov 2020.

Vancouver:

Kim IJ. Herpes simplex virus type 1 glycoprotein gM and the membrane associated protein UL11 are required for virus-induced cell fusion and efficient virus entry. [Internet] [Doctoral dissertation]. Louisiana State University; 2013. [cited 2020 Nov 23]. Available from: etd-11132013-135946 ; https://digitalcommons.lsu.edu/gradschool_dissertations/3897.

Council of Science Editors:

Kim IJ. Herpes simplex virus type 1 glycoprotein gM and the membrane associated protein UL11 are required for virus-induced cell fusion and efficient virus entry. [Doctoral Dissertation]. Louisiana State University; 2013. Available from: etd-11132013-135946 ; https://digitalcommons.lsu.edu/gradschool_dissertations/3897

3. Tartour, Kevin. Identification et caractérisation d’une nouvelle famille de facteur de restriction - les IFITMs : Identification and characterization of a new family of restriction factors - IFITMs.

Degree: Docteur es, Sciences de la Vie, 2014, Lyon, École normale supérieure

Le VIH, comme tous les virus, nécessite la coopération de nombreuses protéines cellulaires pour réaliser son cycle viral. Néanmoins, un panel de protéines est spécifiquement… (more)

Subjects/Keywords: Virus; VIH; Restriction; Immunité innée; IFITM; Fusion; Virus; HIV; Restriction; Innate immunity; IFITM; Fusion

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APA (6th Edition):

Tartour, K. (2014). Identification et caractérisation d’une nouvelle famille de facteur de restriction - les IFITMs : Identification and characterization of a new family of restriction factors - IFITMs. (Doctoral Dissertation). Lyon, École normale supérieure. Retrieved from http://www.theses.fr/2014ENSL0972

Chicago Manual of Style (16th Edition):

Tartour, Kevin. “Identification et caractérisation d’une nouvelle famille de facteur de restriction - les IFITMs : Identification and characterization of a new family of restriction factors - IFITMs.” 2014. Doctoral Dissertation, Lyon, École normale supérieure. Accessed November 23, 2020. http://www.theses.fr/2014ENSL0972.

MLA Handbook (7th Edition):

Tartour, Kevin. “Identification et caractérisation d’une nouvelle famille de facteur de restriction - les IFITMs : Identification and characterization of a new family of restriction factors - IFITMs.” 2014. Web. 23 Nov 2020.

Vancouver:

Tartour K. Identification et caractérisation d’une nouvelle famille de facteur de restriction - les IFITMs : Identification and characterization of a new family of restriction factors - IFITMs. [Internet] [Doctoral dissertation]. Lyon, École normale supérieure; 2014. [cited 2020 Nov 23]. Available from: http://www.theses.fr/2014ENSL0972.

Council of Science Editors:

Tartour K. Identification et caractérisation d’une nouvelle famille de facteur de restriction - les IFITMs : Identification and characterization of a new family of restriction factors - IFITMs. [Doctoral Dissertation]. Lyon, École normale supérieure; 2014. Available from: http://www.theses.fr/2014ENSL0972


Vanderbilt University

4. Cox, Reagan Josephine Greene. Breaking in: human metapneumovirus fusion and entry.

Degree: PhD, Microbiology and Immunology, 2012, Vanderbilt University

 This project is concerned with how the recently discovered paramyxovirus, human metapneumovirus (HMPV), interacts with host cells to initiate entry. In this dissertation I explore… (more)

Subjects/Keywords: integrin; human metapneumovirus; paramyxovirus; virus fusion; virus entry

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APA (6th Edition):

Cox, R. J. G. (2012). Breaking in: human metapneumovirus fusion and entry. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14872

Chicago Manual of Style (16th Edition):

Cox, Reagan Josephine Greene. “Breaking in: human metapneumovirus fusion and entry.” 2012. Doctoral Dissertation, Vanderbilt University. Accessed November 23, 2020. http://hdl.handle.net/1803/14872.

MLA Handbook (7th Edition):

Cox, Reagan Josephine Greene. “Breaking in: human metapneumovirus fusion and entry.” 2012. Web. 23 Nov 2020.

Vancouver:

Cox RJG. Breaking in: human metapneumovirus fusion and entry. [Internet] [Doctoral dissertation]. Vanderbilt University; 2012. [cited 2020 Nov 23]. Available from: http://hdl.handle.net/1803/14872.

Council of Science Editors:

Cox RJG. Breaking in: human metapneumovirus fusion and entry. [Doctoral Dissertation]. Vanderbilt University; 2012. Available from: http://hdl.handle.net/1803/14872


Indian Institute of Science

5. Mulampaka, Shiva Naresh. Theoretical Studies of the Mechanisms of the Entry of Virus into Cells.

Degree: PhD, Faculty of Engineering, 2018, Indian Institute of Science

 Viruses cause human diseases by entering in to human cells. Many drugs have been developed that act at various stages of viral infection, but they… (more)

Subjects/Keywords: Virus Entry; Virus Diseases; Viral Infections; HIV Entry; HIV Fusion/Entry Inhibitors; Cell-Cell Fusion Assays; HIV-1 Entry; Cells - Virus Entry; Virus Entry Pathway; Endocytosis; Viral Fusion; Virology

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APA (6th Edition):

Mulampaka, S. N. (2018). Theoretical Studies of the Mechanisms of the Entry of Virus into Cells. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/3082

Chicago Manual of Style (16th Edition):

Mulampaka, Shiva Naresh. “Theoretical Studies of the Mechanisms of the Entry of Virus into Cells.” 2018. Doctoral Dissertation, Indian Institute of Science. Accessed November 23, 2020. http://etd.iisc.ac.in/handle/2005/3082.

MLA Handbook (7th Edition):

Mulampaka, Shiva Naresh. “Theoretical Studies of the Mechanisms of the Entry of Virus into Cells.” 2018. Web. 23 Nov 2020.

Vancouver:

Mulampaka SN. Theoretical Studies of the Mechanisms of the Entry of Virus into Cells. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2018. [cited 2020 Nov 23]. Available from: http://etd.iisc.ac.in/handle/2005/3082.

Council of Science Editors:

Mulampaka SN. Theoretical Studies of the Mechanisms of the Entry of Virus into Cells. [Doctoral Dissertation]. Indian Institute of Science; 2018. Available from: http://etd.iisc.ac.in/handle/2005/3082


Universiteit Utrecht

6. Burkard, C. Host Factors Invovled in the Entry of Coronaviruses into Mammalian Cells.

Degree: 2015, Universiteit Utrecht

 Enveloped viruses need to fuse with a host cell membrane in order to deliver their genome into the host cell. While some viruses fuse with… (more)

Subjects/Keywords: Coronavirus; Virus entry; Host factors; Endocytosis; Virus-cell fusion; Lysosomal proteases; Cardiotonic steroids

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APA (6th Edition):

Burkard, C. (2015). Host Factors Invovled in the Entry of Coronaviruses into Mammalian Cells. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/327014

Chicago Manual of Style (16th Edition):

Burkard, C. “Host Factors Invovled in the Entry of Coronaviruses into Mammalian Cells.” 2015. Doctoral Dissertation, Universiteit Utrecht. Accessed November 23, 2020. http://dspace.library.uu.nl:8080/handle/1874/327014.

MLA Handbook (7th Edition):

Burkard, C. “Host Factors Invovled in the Entry of Coronaviruses into Mammalian Cells.” 2015. Web. 23 Nov 2020.

Vancouver:

Burkard C. Host Factors Invovled in the Entry of Coronaviruses into Mammalian Cells. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2015. [cited 2020 Nov 23]. Available from: http://dspace.library.uu.nl:8080/handle/1874/327014.

Council of Science Editors:

Burkard C. Host Factors Invovled in the Entry of Coronaviruses into Mammalian Cells. [Doctoral Dissertation]. Universiteit Utrecht; 2015. Available from: http://dspace.library.uu.nl:8080/handle/1874/327014

7. 泉田, 真生. Fragments of target cells are internalized into retroviral envelope protein-expressing cells during cell-cell fusion by endocytosis : レトロウイルスによる細胞融合において、標的細胞の断片がエンベロープ蛋白質発現細胞内にエンドサイトーシスによって取り込まれる.

Degree: 博士(医学), 2016, Nagasaki University / 長崎大学

 Retroviruses enter into host cells by fusion between viral and host cell membranes. Retroviral envelope glycoprotein (Env) induces the membrane fusion, and also mediates cell-cell… (more)

Subjects/Keywords: endocytosis; retrovirus; envelope; cell-cell fusion; murine leukemia virus; human immunodeficiency virus

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APA (6th Edition):

泉田, . (2016). Fragments of target cells are internalized into retroviral envelope protein-expressing cells during cell-cell fusion by endocytosis : レトロウイルスによる細胞融合において、標的細胞の断片がエンベロープ蛋白質発現細胞内にエンドサイトーシスによって取り込まれる. (Thesis). Nagasaki University / 長崎大学. Retrieved from http://hdl.handle.net/10069/36261

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):

泉田, 真生. “Fragments of target cells are internalized into retroviral envelope protein-expressing cells during cell-cell fusion by endocytosis : レトロウイルスによる細胞融合において、標的細胞の断片がエンベロープ蛋白質発現細胞内にエンドサイトーシスによって取り込まれる.” 2016. Thesis, Nagasaki University / 長崎大学. Accessed November 23, 2020. http://hdl.handle.net/10069/36261.

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

MLA Handbook (7th Edition):

泉田, 真生. “Fragments of target cells are internalized into retroviral envelope protein-expressing cells during cell-cell fusion by endocytosis : レトロウイルスによる細胞融合において、標的細胞の断片がエンベロープ蛋白質発現細胞内にエンドサイトーシスによって取り込まれる.” 2016. Web. 23 Nov 2020.

Vancouver:

泉田 . Fragments of target cells are internalized into retroviral envelope protein-expressing cells during cell-cell fusion by endocytosis : レトロウイルスによる細胞融合において、標的細胞の断片がエンベロープ蛋白質発現細胞内にエンドサイトーシスによって取り込まれる. [Internet] [Thesis]. Nagasaki University / 長崎大学; 2016. [cited 2020 Nov 23]. Available from: http://hdl.handle.net/10069/36261.

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

Council of Science Editors:

泉田 . Fragments of target cells are internalized into retroviral envelope protein-expressing cells during cell-cell fusion by endocytosis : レトロウイルスによる細胞融合において、標的細胞の断片がエンベロープ蛋白質発現細胞内にエンドサイトーシスによって取り込まれる. [Thesis]. Nagasaki University / 長崎大学; 2016. Available from: http://hdl.handle.net/10069/36261

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


Loyola University Chicago

8. Hantak, Michael. Membrane Microdomains as Platforms for Extra-Cellular Fusions.

Degree: PhD, Microbiology and Immunology, 2019, Loyola University Chicago

 Life requires biological membranes. Membrane-enclosed compartments separate and unite through dynamic fission and fusion reactions. These are catalyzed processes that are central in organismal biogenesis.… (more)

Subjects/Keywords: Extracellular Vesicle; Membrane Fusion; Osteoclast; Tetraspanin; Virus; Virology

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APA (6th Edition):

Hantak, M. (2019). Membrane Microdomains as Platforms for Extra-Cellular Fusions. (Doctoral Dissertation). Loyola University Chicago. Retrieved from https://ecommons.luc.edu/luc_diss/3337

Chicago Manual of Style (16th Edition):

Hantak, Michael. “Membrane Microdomains as Platforms for Extra-Cellular Fusions.” 2019. Doctoral Dissertation, Loyola University Chicago. Accessed November 23, 2020. https://ecommons.luc.edu/luc_diss/3337.

MLA Handbook (7th Edition):

Hantak, Michael. “Membrane Microdomains as Platforms for Extra-Cellular Fusions.” 2019. Web. 23 Nov 2020.

Vancouver:

Hantak M. Membrane Microdomains as Platforms for Extra-Cellular Fusions. [Internet] [Doctoral dissertation]. Loyola University Chicago; 2019. [cited 2020 Nov 23]. Available from: https://ecommons.luc.edu/luc_diss/3337.

Council of Science Editors:

Hantak M. Membrane Microdomains as Platforms for Extra-Cellular Fusions. [Doctoral Dissertation]. Loyola University Chicago; 2019. Available from: https://ecommons.luc.edu/luc_diss/3337


North Carolina State University

9. Wessels, Laura. A fluorescence microscopy study of the dynamics of low-pH triggered Membrane Fusion.

Degree: PhD, Physics, 2009, North Carolina State University

 Enveloped viruses employ membrane fusion during cell penetration in order to deliver their genetic material across the cell boundary. Large conformational changes in the proteins… (more)

Subjects/Keywords: Influenza; Sindbis virus; single particle experiments; fluorescense microscopy; membrane fusion

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APA (6th Edition):

Wessels, L. (2009). A fluorescence microscopy study of the dynamics of low-pH triggered Membrane Fusion. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/3626

Chicago Manual of Style (16th Edition):

Wessels, Laura. “A fluorescence microscopy study of the dynamics of low-pH triggered Membrane Fusion.” 2009. Doctoral Dissertation, North Carolina State University. Accessed November 23, 2020. http://www.lib.ncsu.edu/resolver/1840.16/3626.

MLA Handbook (7th Edition):

Wessels, Laura. “A fluorescence microscopy study of the dynamics of low-pH triggered Membrane Fusion.” 2009. Web. 23 Nov 2020.

Vancouver:

Wessels L. A fluorescence microscopy study of the dynamics of low-pH triggered Membrane Fusion. [Internet] [Doctoral dissertation]. North Carolina State University; 2009. [cited 2020 Nov 23]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/3626.

Council of Science Editors:

Wessels L. A fluorescence microscopy study of the dynamics of low-pH triggered Membrane Fusion. [Doctoral Dissertation]. North Carolina State University; 2009. Available from: http://www.lib.ncsu.edu/resolver/1840.16/3626


University of the Western Cape

10. Choi, Yook-Wah. Structural and functional characterization of human DDX5 and its interaction with NS5B of hepatitis C virus .

Degree: 2011, University of the Western Cape

 Hepatitis C was first recognized as a transfusion-associated liver disease not caused by hepatitis A or hepatitis B virus after serological tests were developed to… (more)

Subjects/Keywords: Hepatitis C virus (HCV); GST fusion protein; NS5B; Protein crystallisation screens

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APA (6th Edition):

Choi, Y. (2011). Structural and functional characterization of human DDX5 and its interaction with NS5B of hepatitis C virus . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/5299

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):

Choi, Yook-Wah. “Structural and functional characterization of human DDX5 and its interaction with NS5B of hepatitis C virus .” 2011. Thesis, University of the Western Cape. Accessed November 23, 2020. http://hdl.handle.net/11394/5299.

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

MLA Handbook (7th Edition):

Choi, Yook-Wah. “Structural and functional characterization of human DDX5 and its interaction with NS5B of hepatitis C virus .” 2011. Web. 23 Nov 2020.

Vancouver:

Choi Y. Structural and functional characterization of human DDX5 and its interaction with NS5B of hepatitis C virus . [Internet] [Thesis]. University of the Western Cape; 2011. [cited 2020 Nov 23]. Available from: http://hdl.handle.net/11394/5299.

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

Council of Science Editors:

Choi Y. Structural and functional characterization of human DDX5 and its interaction with NS5B of hepatitis C virus . [Thesis]. University of the Western Cape; 2011. Available from: http://hdl.handle.net/11394/5299

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


University of Toronto

11. Aydin, Halil. Structural and Functional Insights into the Molecular Mechanisms of Viral-cell and Cell-cell Fusion.

Degree: PhD, 2016, University of Toronto

Membrane fusion is an essential step in various developmental, physiological, and pathological processes in eukaryotes. Specific fusion proteins catalyze the merger of two lipid bilayers.… (more)

Subjects/Keywords: fertilization; Fusion; glycoprotein; Membrane; structural biology; Virus; 0487

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APA (6th Edition):

Aydin, H. (2016). Structural and Functional Insights into the Molecular Mechanisms of Viral-cell and Cell-cell Fusion. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/80388

Chicago Manual of Style (16th Edition):

Aydin, Halil. “Structural and Functional Insights into the Molecular Mechanisms of Viral-cell and Cell-cell Fusion.” 2016. Doctoral Dissertation, University of Toronto. Accessed November 23, 2020. http://hdl.handle.net/1807/80388.

MLA Handbook (7th Edition):

Aydin, Halil. “Structural and Functional Insights into the Molecular Mechanisms of Viral-cell and Cell-cell Fusion.” 2016. Web. 23 Nov 2020.

Vancouver:

Aydin H. Structural and Functional Insights into the Molecular Mechanisms of Viral-cell and Cell-cell Fusion. [Internet] [Doctoral dissertation]. University of Toronto; 2016. [cited 2020 Nov 23]. Available from: http://hdl.handle.net/1807/80388.

Council of Science Editors:

Aydin H. Structural and Functional Insights into the Molecular Mechanisms of Viral-cell and Cell-cell Fusion. [Doctoral Dissertation]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/80388


University of South Florida

12. Monfort, Dagmara Anne. Recombinant Elastin Based Nanoparticles for Targeted Gene Therapy.

Degree: 2017, University of South Florida

 Gene therapy is a technique used to inactivate, replace or insert a corrective copy of a defective gene in order to help diseased tissues to… (more)

Subjects/Keywords: Fusion proteins; growth factors; transduction; drug delivery; virus; Engineering

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APA (6th Edition):

Monfort, D. A. (2017). Recombinant Elastin Based Nanoparticles for Targeted Gene Therapy. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/6627

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):

Monfort, Dagmara Anne. “Recombinant Elastin Based Nanoparticles for Targeted Gene Therapy.” 2017. Thesis, University of South Florida. Accessed November 23, 2020. https://scholarcommons.usf.edu/etd/6627.

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

MLA Handbook (7th Edition):

Monfort, Dagmara Anne. “Recombinant Elastin Based Nanoparticles for Targeted Gene Therapy.” 2017. Web. 23 Nov 2020.

Vancouver:

Monfort DA. Recombinant Elastin Based Nanoparticles for Targeted Gene Therapy. [Internet] [Thesis]. University of South Florida; 2017. [cited 2020 Nov 23]. Available from: https://scholarcommons.usf.edu/etd/6627.

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

Council of Science Editors:

Monfort DA. Recombinant Elastin Based Nanoparticles for Targeted Gene Therapy. [Thesis]. University of South Florida; 2017. Available from: https://scholarcommons.usf.edu/etd/6627

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


University of Alberta

13. St.Vincent, Mireille RM. The Discovery and Characterization of Rigid Amphipathic Fusion Inhibitors (RAFIS), a Novel Class of Broad-Spectrum Antiviral Compounds.

Degree: PhD, Department of Biochemistry, 2012, University of Alberta

 Antiviral drugs targeting viral proteins or their interactions with cellular proteins lead to rapid selection for resistance. Moreover, the number of viral targets is limited.… (more)

Subjects/Keywords: RNA virus; small molecule compounds; Hepatitis C virus; lipid bilayer curvature; Rigid Amphipathic Fusion Inbitors (RAFIs); DNA virus

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APA (6th Edition):

St.Vincent, M. R. (2012). The Discovery and Characterization of Rigid Amphipathic Fusion Inhibitors (RAFIS), a Novel Class of Broad-Spectrum Antiviral Compounds. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/db78td54v

Chicago Manual of Style (16th Edition):

St.Vincent, Mireille RM. “The Discovery and Characterization of Rigid Amphipathic Fusion Inhibitors (RAFIS), a Novel Class of Broad-Spectrum Antiviral Compounds.” 2012. Doctoral Dissertation, University of Alberta. Accessed November 23, 2020. https://era.library.ualberta.ca/files/db78td54v.

MLA Handbook (7th Edition):

St.Vincent, Mireille RM. “The Discovery and Characterization of Rigid Amphipathic Fusion Inhibitors (RAFIS), a Novel Class of Broad-Spectrum Antiviral Compounds.” 2012. Web. 23 Nov 2020.

Vancouver:

St.Vincent MR. The Discovery and Characterization of Rigid Amphipathic Fusion Inhibitors (RAFIS), a Novel Class of Broad-Spectrum Antiviral Compounds. [Internet] [Doctoral dissertation]. University of Alberta; 2012. [cited 2020 Nov 23]. Available from: https://era.library.ualberta.ca/files/db78td54v.

Council of Science Editors:

St.Vincent MR. The Discovery and Characterization of Rigid Amphipathic Fusion Inhibitors (RAFIS), a Novel Class of Broad-Spectrum Antiviral Compounds. [Doctoral Dissertation]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/db78td54v


Penn State University

14. Sun, Weina. Henipavirus assembly and budding.

Degree: 2015, Penn State University

 The emergence of a group of paramyxoviruses called henipavirus has caused fatal illness such as severe vasculitis and encephalitis which resulted in high fatality rate… (more)

Subjects/Keywords: Henipavirus; Hendra virus; Nipah virus; assembly and budding; paramyxovirus; AP-3 complex; Hendra virus fusion protein; Rab11a

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APA (6th Edition):

Sun, W. (2015). Henipavirus assembly and budding. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/24959

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):

Sun, Weina. “Henipavirus assembly and budding.” 2015. Thesis, Penn State University. Accessed November 23, 2020. https://submit-etda.libraries.psu.edu/catalog/24959.

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

MLA Handbook (7th Edition):

Sun, Weina. “Henipavirus assembly and budding.” 2015. Web. 23 Nov 2020.

Vancouver:

Sun W. Henipavirus assembly and budding. [Internet] [Thesis]. Penn State University; 2015. [cited 2020 Nov 23]. Available from: https://submit-etda.libraries.psu.edu/catalog/24959.

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

Council of Science Editors:

Sun W. Henipavirus assembly and budding. [Thesis]. Penn State University; 2015. Available from: https://submit-etda.libraries.psu.edu/catalog/24959

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

15. Gui, Long. Structural Insights into Viral Membrane Fusion Machinery via Cryo-Electron Tomography: Influenza Virus and Human Parainfluenza Virus.

Degree: PhD, 2016, University of Washington

 Enveloped viruses such as influenza virus and human parainfluenza virus utilize specialized protein machinery to fuse their membrane with the cellular membrane of target host… (more)

Subjects/Keywords: cryo-electron microscopy; cryo-electron tomography; human parainfluenza virus; influenza virus; membrane fusion; Biophysics; Virology; medicinal chemistry

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APA (6th Edition):

Gui, L. (2016). Structural Insights into Viral Membrane Fusion Machinery via Cryo-Electron Tomography: Influenza Virus and Human Parainfluenza Virus. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/36768

Chicago Manual of Style (16th Edition):

Gui, Long. “Structural Insights into Viral Membrane Fusion Machinery via Cryo-Electron Tomography: Influenza Virus and Human Parainfluenza Virus.” 2016. Doctoral Dissertation, University of Washington. Accessed November 23, 2020. http://hdl.handle.net/1773/36768.

MLA Handbook (7th Edition):

Gui, Long. “Structural Insights into Viral Membrane Fusion Machinery via Cryo-Electron Tomography: Influenza Virus and Human Parainfluenza Virus.” 2016. Web. 23 Nov 2020.

Vancouver:

Gui L. Structural Insights into Viral Membrane Fusion Machinery via Cryo-Electron Tomography: Influenza Virus and Human Parainfluenza Virus. [Internet] [Doctoral dissertation]. University of Washington; 2016. [cited 2020 Nov 23]. Available from: http://hdl.handle.net/1773/36768.

Council of Science Editors:

Gui L. Structural Insights into Viral Membrane Fusion Machinery via Cryo-Electron Tomography: Influenza Virus and Human Parainfluenza Virus. [Doctoral Dissertation]. University of Washington; 2016. Available from: http://hdl.handle.net/1773/36768

16. Dubois, Julia. Étude de l'infection par le métapneumovirus humain : facteurs de virulence et développement de vaccins vivants atténués : Study of hMPV infection and virulence factors for live-attenuated vaccines development.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2018, Lyon; Université Laval (Québec, Canada)

Le métapneumovirus humain (hMPV) est un virus responsable d'infections aiguës des voies respiratoires telles que des bronchiolites, des bronchites ou des pneumonies, principalement chez les… (more)

Subjects/Keywords: Métapneumovirus humain; Pneumovirus; Pneumonie virale; Protéine de fusion; Virus atténué; Vaccin; Génétique inverse; Human metapneumovirus; Pneumovirus; Viral pneumonia; Fusion protein; Attenuated virus; Vaccine; Reverse genetics; 571.6

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APA (6th Edition):

Dubois, J. (2018). Étude de l'infection par le métapneumovirus humain : facteurs de virulence et développement de vaccins vivants atténués : Study of hMPV infection and virulence factors for live-attenuated vaccines development. (Doctoral Dissertation). Lyon; Université Laval (Québec, Canada). Retrieved from http://www.theses.fr/2018LYSE1018

Chicago Manual of Style (16th Edition):

Dubois, Julia. “Étude de l'infection par le métapneumovirus humain : facteurs de virulence et développement de vaccins vivants atténués : Study of hMPV infection and virulence factors for live-attenuated vaccines development.” 2018. Doctoral Dissertation, Lyon; Université Laval (Québec, Canada). Accessed November 23, 2020. http://www.theses.fr/2018LYSE1018.

MLA Handbook (7th Edition):

Dubois, Julia. “Étude de l'infection par le métapneumovirus humain : facteurs de virulence et développement de vaccins vivants atténués : Study of hMPV infection and virulence factors for live-attenuated vaccines development.” 2018. Web. 23 Nov 2020.

Vancouver:

Dubois J. Étude de l'infection par le métapneumovirus humain : facteurs de virulence et développement de vaccins vivants atténués : Study of hMPV infection and virulence factors for live-attenuated vaccines development. [Internet] [Doctoral dissertation]. Lyon; Université Laval (Québec, Canada); 2018. [cited 2020 Nov 23]. Available from: http://www.theses.fr/2018LYSE1018.

Council of Science Editors:

Dubois J. Étude de l'infection par le métapneumovirus humain : facteurs de virulence et développement de vaccins vivants atténués : Study of hMPV infection and virulence factors for live-attenuated vaccines development. [Doctoral Dissertation]. Lyon; Université Laval (Québec, Canada); 2018. Available from: http://www.theses.fr/2018LYSE1018


Vanderbilt University

17. Shaikh, Fyza Yusuf. The role of the respiratory syncytial virus fusion protein in viral filamentous assembly.

Degree: PhD, Microbiology and Immunology, 2012, Vanderbilt University

 Respiratory syncytial virus (RSV) is a single-stranded RNA virus in the Paramyxoviridae family that is a leading cause of pneumonia and bronchiolitis in infants and… (more)

Subjects/Keywords: filaments; cytoplasmic tail; paramyxovirus; respiratory syncytial virus; fusion protein; assembly and budding

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APA (6th Edition):

Shaikh, F. Y. (2012). The role of the respiratory syncytial virus fusion protein in viral filamentous assembly. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12371

Chicago Manual of Style (16th Edition):

Shaikh, Fyza Yusuf. “The role of the respiratory syncytial virus fusion protein in viral filamentous assembly.” 2012. Doctoral Dissertation, Vanderbilt University. Accessed November 23, 2020. http://hdl.handle.net/1803/12371.

MLA Handbook (7th Edition):

Shaikh, Fyza Yusuf. “The role of the respiratory syncytial virus fusion protein in viral filamentous assembly.” 2012. Web. 23 Nov 2020.

Vancouver:

Shaikh FY. The role of the respiratory syncytial virus fusion protein in viral filamentous assembly. [Internet] [Doctoral dissertation]. Vanderbilt University; 2012. [cited 2020 Nov 23]. Available from: http://hdl.handle.net/1803/12371.

Council of Science Editors:

Shaikh FY. The role of the respiratory syncytial virus fusion protein in viral filamentous assembly. [Doctoral Dissertation]. Vanderbilt University; 2012. Available from: http://hdl.handle.net/1803/12371


University of Vermont

18. Symeonides, Menelaos. HIV-1-Induced Cell-Cell Fusion: Host Regulation And Consequences For Viral Spread.

Degree: PhD, Cellular, Molecular and Biomedical Sciences, 2016, University of Vermont

  Human immunodeficiency virus type 1 (HIV-1) is a human retrovirus of the lentivirus subgroup which primarily infects T cells and macrophages, and causes acquired… (more)

Subjects/Keywords: cell fusion; HIV; lymphocyte; syncytia; tetraspanin; virus transmission; Cell Biology; Microbiology; Virology

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APA (6th Edition):

Symeonides, M. (2016). HIV-1-Induced Cell-Cell Fusion: Host Regulation And Consequences For Viral Spread. (Doctoral Dissertation). University of Vermont. Retrieved from https://scholarworks.uvm.edu/graddis/589

Chicago Manual of Style (16th Edition):

Symeonides, Menelaos. “HIV-1-Induced Cell-Cell Fusion: Host Regulation And Consequences For Viral Spread.” 2016. Doctoral Dissertation, University of Vermont. Accessed November 23, 2020. https://scholarworks.uvm.edu/graddis/589.

MLA Handbook (7th Edition):

Symeonides, Menelaos. “HIV-1-Induced Cell-Cell Fusion: Host Regulation And Consequences For Viral Spread.” 2016. Web. 23 Nov 2020.

Vancouver:

Symeonides M. HIV-1-Induced Cell-Cell Fusion: Host Regulation And Consequences For Viral Spread. [Internet] [Doctoral dissertation]. University of Vermont; 2016. [cited 2020 Nov 23]. Available from: https://scholarworks.uvm.edu/graddis/589.

Council of Science Editors:

Symeonides M. HIV-1-Induced Cell-Cell Fusion: Host Regulation And Consequences For Viral Spread. [Doctoral Dissertation]. University of Vermont; 2016. Available from: https://scholarworks.uvm.edu/graddis/589

19. Krishna, Benjamin Anthony Cates. Investigating and exploiting the latency-associated expression of the human cytomegalovirus gene US28 in early myeloid lineage cells.

Degree: PhD, 2017, University of Cambridge

 Human cytomegalovirus (HCMV) is a betaherpesvirus which establishes a lifelong persistent infection, underpinned by its ability to establish latent infection in early myeloid lineage cells,… (more)

Subjects/Keywords: virus; virology; cytomegalovirus; therapeutic; latent; latency; hcmv; US28; immunotherapeutic; fusion toxin protein

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

APA (6th Edition):

Krishna, B. A. C. (2017). Investigating and exploiting the latency-associated expression of the human cytomegalovirus gene US28 in early myeloid lineage cells. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/267737

Chicago Manual of Style (16th Edition):

Krishna, Benjamin Anthony Cates. “Investigating and exploiting the latency-associated expression of the human cytomegalovirus gene US28 in early myeloid lineage cells.” 2017. Doctoral Dissertation, University of Cambridge. Accessed November 23, 2020. https://www.repository.cam.ac.uk/handle/1810/267737.

MLA Handbook (7th Edition):

Krishna, Benjamin Anthony Cates. “Investigating and exploiting the latency-associated expression of the human cytomegalovirus gene US28 in early myeloid lineage cells.” 2017. Web. 23 Nov 2020.

Vancouver:

Krishna BAC. Investigating and exploiting the latency-associated expression of the human cytomegalovirus gene US28 in early myeloid lineage cells. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2020 Nov 23]. Available from: https://www.repository.cam.ac.uk/handle/1810/267737.

Council of Science Editors:

Krishna BAC. Investigating and exploiting the latency-associated expression of the human cytomegalovirus gene US28 in early myeloid lineage cells. [Doctoral Dissertation]. University of Cambridge; 2017. Available from: https://www.repository.cam.ac.uk/handle/1810/267737


University of Maryland

20. Manoharan, Vinoth Kumar. IMPROVED NEWCASTLE DISEASE VIRUS VACCINES AND VECTORS.

Degree: Veterinary Medical Science, 2017, University of Maryland

 Newcastle disease (ND) is an economically important disease of poultry worldwide. The use of vaccines to control ND is necessary because of frequent outbreaks of… (more)

Subjects/Keywords: Veterinary science; Virology; cleavage site; fusion protein; NDV vaccine; Newcastle disease virus; SIV; vector

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APA (6th Edition):

Manoharan, V. K. (2017). IMPROVED NEWCASTLE DISEASE VIRUS VACCINES AND VECTORS. (Thesis). University of Maryland. Retrieved from http://hdl.handle.net/1903/20294

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):

Manoharan, Vinoth Kumar. “IMPROVED NEWCASTLE DISEASE VIRUS VACCINES AND VECTORS.” 2017. Thesis, University of Maryland. Accessed November 23, 2020. http://hdl.handle.net/1903/20294.

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

MLA Handbook (7th Edition):

Manoharan, Vinoth Kumar. “IMPROVED NEWCASTLE DISEASE VIRUS VACCINES AND VECTORS.” 2017. Web. 23 Nov 2020.

Vancouver:

Manoharan VK. IMPROVED NEWCASTLE DISEASE VIRUS VACCINES AND VECTORS. [Internet] [Thesis]. University of Maryland; 2017. [cited 2020 Nov 23]. Available from: http://hdl.handle.net/1903/20294.

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

Council of Science Editors:

Manoharan VK. IMPROVED NEWCASTLE DISEASE VIRUS VACCINES AND VECTORS. [Thesis]. University of Maryland; 2017. Available from: http://hdl.handle.net/1903/20294

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


University of Cambridge

21. Krishna, Benjamin Anthony Cates. Investigating and exploiting the latency-associated expression of the human cytomegalovirus gene US28 in early myeloid lineage cells.

Degree: PhD, 2017, University of Cambridge

 Human cytomegalovirus (HCMV) is a betaherpesvirus which establishes a lifelong persistent infection, underpinned by its ability to establish latent infection in early myeloid lineage cells,… (more)

Subjects/Keywords: 616.9; virus; virology; cytomegalovirus; therapeutic; latent; latency; hcmv; US28; immunotherapeutic; fusion toxin protein

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APA (6th Edition):

Krishna, B. A. C. (2017). Investigating and exploiting the latency-associated expression of the human cytomegalovirus gene US28 in early myeloid lineage cells. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.13670 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.725527

Chicago Manual of Style (16th Edition):

Krishna, Benjamin Anthony Cates. “Investigating and exploiting the latency-associated expression of the human cytomegalovirus gene US28 in early myeloid lineage cells.” 2017. Doctoral Dissertation, University of Cambridge. Accessed November 23, 2020. https://doi.org/10.17863/CAM.13670 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.725527.

MLA Handbook (7th Edition):

Krishna, Benjamin Anthony Cates. “Investigating and exploiting the latency-associated expression of the human cytomegalovirus gene US28 in early myeloid lineage cells.” 2017. Web. 23 Nov 2020.

Vancouver:

Krishna BAC. Investigating and exploiting the latency-associated expression of the human cytomegalovirus gene US28 in early myeloid lineage cells. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2020 Nov 23]. Available from: https://doi.org/10.17863/CAM.13670 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.725527.

Council of Science Editors:

Krishna BAC. Investigating and exploiting the latency-associated expression of the human cytomegalovirus gene US28 in early myeloid lineage cells. [Doctoral Dissertation]. University of Cambridge; 2017. Available from: https://doi.org/10.17863/CAM.13670 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.725527


The Ohio State University

22. Costello, Heather M. The N500 Glycan of the Respiratory Syncytial Virus F Protein is Required for Fusion, but Not for Stabilization or Triggering of the Protein.

Degree: PhD, Integrated Biomedical Science Graduate Program, 2013, The Ohio State University

 Respiratory syncytial virus (RSV), a paramyxovirus, is the most significant respiratory pathogen in infants and causes 90,000 emergency hospitalizations in the United States and 160,000… (more)

Subjects/Keywords: Virology; Biomedical Research; respiratory syncytial virus; fusion protein; paramyxovirus; viral entry; antiviral; vaccine; N-glycan

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APA (6th Edition):

Costello, H. M. (2013). The N500 Glycan of the Respiratory Syncytial Virus F Protein is Required for Fusion, but Not for Stabilization or Triggering of the Protein. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1376568814

Chicago Manual of Style (16th Edition):

Costello, Heather M. “The N500 Glycan of the Respiratory Syncytial Virus F Protein is Required for Fusion, but Not for Stabilization or Triggering of the Protein.” 2013. Doctoral Dissertation, The Ohio State University. Accessed November 23, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1376568814.

MLA Handbook (7th Edition):

Costello, Heather M. “The N500 Glycan of the Respiratory Syncytial Virus F Protein is Required for Fusion, but Not for Stabilization or Triggering of the Protein.” 2013. Web. 23 Nov 2020.

Vancouver:

Costello HM. The N500 Glycan of the Respiratory Syncytial Virus F Protein is Required for Fusion, but Not for Stabilization or Triggering of the Protein. [Internet] [Doctoral dissertation]. The Ohio State University; 2013. [cited 2020 Nov 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1376568814.

Council of Science Editors:

Costello HM. The N500 Glycan of the Respiratory Syncytial Virus F Protein is Required for Fusion, but Not for Stabilization or Triggering of the Protein. [Doctoral Dissertation]. The Ohio State University; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1376568814

23. 佐藤, 友人. 麻疹ウイルスF蛋白の膜融合活性発現の分子機構 : Molecular mechanism of expression of membranefusion activity by fusion protein of measles virus.

Degree: 博士(バイオサイエンス), 2015, Nagahama Institute of Bio-Science and Technology / 長浜バイオ大学

2014

Subjects/Keywords: Measles virus; Fusion protein; Membrane fusion; Refolding; Thermodynamic stability; Measles virus; Fusion protein; Membrane fusion; Refolding; Thermodynamic stability

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APA (6th Edition):

佐藤, . (2015). 麻疹ウイルスF蛋白の膜融合活性発現の分子機構 : Molecular mechanism of expression of membranefusion activity by fusion protein of measles virus. (Thesis). Nagahama Institute of Bio-Science and Technology / 長浜バイオ大学. Retrieved from http://id.nii.ac.jp/1211/00000017/

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):

佐藤, 友人. “麻疹ウイルスF蛋白の膜融合活性発現の分子機構 : Molecular mechanism of expression of membranefusion activity by fusion protein of measles virus.” 2015. Thesis, Nagahama Institute of Bio-Science and Technology / 長浜バイオ大学. Accessed November 23, 2020. http://id.nii.ac.jp/1211/00000017/.

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

MLA Handbook (7th Edition):

佐藤, 友人. “麻疹ウイルスF蛋白の膜融合活性発現の分子機構 : Molecular mechanism of expression of membranefusion activity by fusion protein of measles virus.” 2015. Web. 23 Nov 2020.

Vancouver:

佐藤 . 麻疹ウイルスF蛋白の膜融合活性発現の分子機構 : Molecular mechanism of expression of membranefusion activity by fusion protein of measles virus. [Internet] [Thesis]. Nagahama Institute of Bio-Science and Technology / 長浜バイオ大学; 2015. [cited 2020 Nov 23]. Available from: http://id.nii.ac.jp/1211/00000017/.

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

Council of Science Editors:

佐藤 . 麻疹ウイルスF蛋白の膜融合活性発現の分子機構 : Molecular mechanism of expression of membranefusion activity by fusion protein of measles virus. [Thesis]. Nagahama Institute of Bio-Science and Technology / 長浜バイオ大学; 2015. Available from: http://id.nii.ac.jp/1211/00000017/

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


University of Oxford

24. Bitto, David. In vitro analysis of viral fusion and receptor binding with a focus on selected arthropod-borne viruses of the families Bunyaviridae and Togaviridae.

Degree: PhD, 2014, University of Oxford

 Emerging arthropod-borne viruses, such as alphaviruses and bunyaviruses, represent a serious threat to human and animal health worldwide, and for most of them, vaccines and… (more)

Subjects/Keywords: 616.9; Life Sciences; Medical sciences; Viruses; Infectious diseases; Biochemistry; Virus entry; Bunyaviridae; Phlebovirus; Uukuniemi virus; Alphavirus; Semliki Forest virus; Membrane fusion; Electron cryomicroscopy; Electron cryotomography; Icosahedral reconstruction

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APA (6th Edition):

Bitto, D. (2014). In vitro analysis of viral fusion and receptor binding with a focus on selected arthropod-borne viruses of the families Bunyaviridae and Togaviridae. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:40875104-1eb6-47f6-b1e7-d26147c002a8 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635269

Chicago Manual of Style (16th Edition):

Bitto, David. “In vitro analysis of viral fusion and receptor binding with a focus on selected arthropod-borne viruses of the families Bunyaviridae and Togaviridae.” 2014. Doctoral Dissertation, University of Oxford. Accessed November 23, 2020. http://ora.ox.ac.uk/objects/uuid:40875104-1eb6-47f6-b1e7-d26147c002a8 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635269.

MLA Handbook (7th Edition):

Bitto, David. “In vitro analysis of viral fusion and receptor binding with a focus on selected arthropod-borne viruses of the families Bunyaviridae and Togaviridae.” 2014. Web. 23 Nov 2020.

Vancouver:

Bitto D. In vitro analysis of viral fusion and receptor binding with a focus on selected arthropod-borne viruses of the families Bunyaviridae and Togaviridae. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2020 Nov 23]. Available from: http://ora.ox.ac.uk/objects/uuid:40875104-1eb6-47f6-b1e7-d26147c002a8 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635269.

Council of Science Editors:

Bitto D. In vitro analysis of viral fusion and receptor binding with a focus on selected arthropod-borne viruses of the families Bunyaviridae and Togaviridae. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:40875104-1eb6-47f6-b1e7-d26147c002a8 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635269


University of Michigan

25. Lopez, Santiago R. Structure and function of the C -terminal region of a fusion receptor for herpes simplex virus.

Degree: PhD, Virology, 2007, University of Michigan

 Herpes simplex virus (HSV) enters most human cells through pH-independent membrane fusion that requires four viral glycoproteins, a receptor for gD, and other unknown cellular… (more)

Subjects/Keywords: C-terminal; Function; Fusion Receptor; Herpes Simplex Virus; Membrane Fusion; Region; Structure

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APA (6th Edition):

Lopez, S. R. (2007). Structure and function of the C -terminal region of a fusion receptor for herpes simplex virus. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/126499

Chicago Manual of Style (16th Edition):

Lopez, Santiago R. “Structure and function of the C -terminal region of a fusion receptor for herpes simplex virus.” 2007. Doctoral Dissertation, University of Michigan. Accessed November 23, 2020. http://hdl.handle.net/2027.42/126499.

MLA Handbook (7th Edition):

Lopez, Santiago R. “Structure and function of the C -terminal region of a fusion receptor for herpes simplex virus.” 2007. Web. 23 Nov 2020.

Vancouver:

Lopez SR. Structure and function of the C -terminal region of a fusion receptor for herpes simplex virus. [Internet] [Doctoral dissertation]. University of Michigan; 2007. [cited 2020 Nov 23]. Available from: http://hdl.handle.net/2027.42/126499.

Council of Science Editors:

Lopez SR. Structure and function of the C -terminal region of a fusion receptor for herpes simplex virus. [Doctoral Dissertation]. University of Michigan; 2007. Available from: http://hdl.handle.net/2027.42/126499


Virginia Commonwealth University

26. Dollery, Stephen. Identification and characterization of low pH-triggered conformational changes in the herpes simplex virus glycoprotein B.

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

 Herpesviruses can enter host cells by pH-dependent endocytic pathways in a cell-specific manner. The role of pH in herpesvirus endocytosis is unclear. Herpes simplex virus(more)

Subjects/Keywords: herpes; simplex; glycoprotein; gB; virus entry; low pH; conformation; endocytosis; fusion; membrane fusion; s-gB; gB730; HSV; HSV-1; Medicine and Health Sciences

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APA (6th Edition):

Dollery, S. (2011). Identification and characterization of low pH-triggered conformational changes in the herpes simplex virus glycoprotein B. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://doi.org/10.25772/N926-WH48 ; https://scholarscompass.vcu.edu/etd/176

Chicago Manual of Style (16th Edition):

Dollery, Stephen. “Identification and characterization of low pH-triggered conformational changes in the herpes simplex virus glycoprotein B.” 2011. Doctoral Dissertation, Virginia Commonwealth University. Accessed November 23, 2020. https://doi.org/10.25772/N926-WH48 ; https://scholarscompass.vcu.edu/etd/176.

MLA Handbook (7th Edition):

Dollery, Stephen. “Identification and characterization of low pH-triggered conformational changes in the herpes simplex virus glycoprotein B.” 2011. Web. 23 Nov 2020.

Vancouver:

Dollery S. Identification and characterization of low pH-triggered conformational changes in the herpes simplex virus glycoprotein B. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2011. [cited 2020 Nov 23]. Available from: https://doi.org/10.25772/N926-WH48 ; https://scholarscompass.vcu.edu/etd/176.

Council of Science Editors:

Dollery S. Identification and characterization of low pH-triggered conformational changes in the herpes simplex virus glycoprotein B. [Doctoral Dissertation]. Virginia Commonwealth University; 2011. Available from: https://doi.org/10.25772/N926-WH48 ; https://scholarscompass.vcu.edu/etd/176

27. Gonçalves, Raquel Mesquita. Mecanismos de entrada de vírus nas células e suas implicações terapêuticas.

Degree: 2015, Universidade Fernando Pessoa

Projeto de Pós-Graduação/Dissertação apresentado à Universidade Fernando Pessoa como parte dos requisitos para obtenção do grau de Mestre em Ciências Farmacêuticas

Os vírus são parasitas… (more)

Subjects/Keywords: Vírus; Entrada viral; Infeção viral; Parasitas intracelulares; Fusão; Endocitose; Virus; Viral entry; Viral infection; Intracellular parasites; Fusion; Endocytosis

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

APA (6th Edition):

Gonçalves, R. M. (2015). Mecanismos de entrada de vírus nas células e suas implicações terapêuticas. (Thesis). Universidade Fernando Pessoa. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:bdigital.ufp.pt:10284/5153

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):

Gonçalves, Raquel Mesquita. “Mecanismos de entrada de vírus nas células e suas implicações terapêuticas.” 2015. Thesis, Universidade Fernando Pessoa. Accessed November 23, 2020. http://www.rcaap.pt/detail.jsp?id=oai:bdigital.ufp.pt:10284/5153.

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

MLA Handbook (7th Edition):

Gonçalves, Raquel Mesquita. “Mecanismos de entrada de vírus nas células e suas implicações terapêuticas.” 2015. Web. 23 Nov 2020.

Vancouver:

Gonçalves RM. Mecanismos de entrada de vírus nas células e suas implicações terapêuticas. [Internet] [Thesis]. Universidade Fernando Pessoa; 2015. [cited 2020 Nov 23]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:bdigital.ufp.pt:10284/5153.

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

Council of Science Editors:

Gonçalves RM. Mecanismos de entrada de vírus nas células e suas implicações terapêuticas. [Thesis]. Universidade Fernando Pessoa; 2015. Available from: http://www.rcaap.pt/detail.jsp?id=oai:bdigital.ufp.pt:10284/5153

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


Iowa State University

28. Sitthicharoenchai, Panchan. Therapeutic efficacy of small molecule inhibitors of human respiratory syncytial virus (hRSV) in neonatal lambs.

Degree: 2019, Iowa State University

 Human respiratory syncytial virus (hRSV) is a common cause of respiratory infection in human infants worldwide. Direct therapeutic methods for the prevention and treatment such… (more)

Subjects/Keywords: Fusion protein inhibitor; Human respiratory syncytial virus; Neonatal lamb model; Small molecule antiviral inhibitor; Pathology; Pharmacy and Pharmaceutical Sciences; Veterinary Medicine

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

APA (6th Edition):

Sitthicharoenchai, P. (2019). Therapeutic efficacy of small molecule inhibitors of human respiratory syncytial virus (hRSV) in neonatal lambs. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/17320

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):

Sitthicharoenchai, Panchan. “Therapeutic efficacy of small molecule inhibitors of human respiratory syncytial virus (hRSV) in neonatal lambs.” 2019. Thesis, Iowa State University. Accessed November 23, 2020. https://lib.dr.iastate.edu/etd/17320.

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

MLA Handbook (7th Edition):

Sitthicharoenchai, Panchan. “Therapeutic efficacy of small molecule inhibitors of human respiratory syncytial virus (hRSV) in neonatal lambs.” 2019. Web. 23 Nov 2020.

Vancouver:

Sitthicharoenchai P. Therapeutic efficacy of small molecule inhibitors of human respiratory syncytial virus (hRSV) in neonatal lambs. [Internet] [Thesis]. Iowa State University; 2019. [cited 2020 Nov 23]. Available from: https://lib.dr.iastate.edu/etd/17320.

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

Council of Science Editors:

Sitthicharoenchai P. Therapeutic efficacy of small molecule inhibitors of human respiratory syncytial virus (hRSV) in neonatal lambs. [Thesis]. Iowa State University; 2019. Available from: https://lib.dr.iastate.edu/etd/17320

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


University of Western Ontario

29. Kambli, Ankita Suryakant. Utilizing FIV (Feline Immunodeficiency Virus) to develop a novel animal model to study HIV (Human Immunodeficiency Virus).

Degree: 2019, University of Western Ontario

 This project sought to perform the in vitro work needed to accomplish the long-term vision of harnessing the similarities between HIV (Human Immunodeficiency Virus) and… (more)

Subjects/Keywords: FIV; HIV; CD4; CCR5; Cell-fusion; Envelope; Cat; FHIV; FHIVenv; Immune System Diseases; Life Sciences; Virology; Virus Diseases

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

APA (6th Edition):

Kambli, A. S. (2019). Utilizing FIV (Feline Immunodeficiency Virus) to develop a novel animal model to study HIV (Human Immunodeficiency Virus). (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/6737

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):

Kambli, Ankita Suryakant. “Utilizing FIV (Feline Immunodeficiency Virus) to develop a novel animal model to study HIV (Human Immunodeficiency Virus).” 2019. Thesis, University of Western Ontario. Accessed November 23, 2020. https://ir.lib.uwo.ca/etd/6737.

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

MLA Handbook (7th Edition):

Kambli, Ankita Suryakant. “Utilizing FIV (Feline Immunodeficiency Virus) to develop a novel animal model to study HIV (Human Immunodeficiency Virus).” 2019. Web. 23 Nov 2020.

Vancouver:

Kambli AS. Utilizing FIV (Feline Immunodeficiency Virus) to develop a novel animal model to study HIV (Human Immunodeficiency Virus). [Internet] [Thesis]. University of Western Ontario; 2019. [cited 2020 Nov 23]. Available from: https://ir.lib.uwo.ca/etd/6737.

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

Council of Science Editors:

Kambli AS. Utilizing FIV (Feline Immunodeficiency Virus) to develop a novel animal model to study HIV (Human Immunodeficiency Virus). [Thesis]. University of Western Ontario; 2019. Available from: https://ir.lib.uwo.ca/etd/6737

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


University of Melbourne

30. Chojnacki, Jakub. Envelope protein domains of duck hepatitis B virus: role in assembly and infectivity.

Degree: 2005, University of Melbourne

 Hepatitis B virus (HBV) is a global public health problem with an estimated number of 350 million carriers world wide who are at risk of… (more)

Subjects/Keywords: duck hepatitis B virus; entry; fusion; assembly; envelope structure

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

APA (6th Edition):

Chojnacki, J. (2005). Envelope protein domains of duck hepatitis B virus: role in assembly and infectivity. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/39048

Chicago Manual of Style (16th Edition):

Chojnacki, Jakub. “Envelope protein domains of duck hepatitis B virus: role in assembly and infectivity.” 2005. Doctoral Dissertation, University of Melbourne. Accessed November 23, 2020. http://hdl.handle.net/11343/39048.

MLA Handbook (7th Edition):

Chojnacki, Jakub. “Envelope protein domains of duck hepatitis B virus: role in assembly and infectivity.” 2005. Web. 23 Nov 2020.

Vancouver:

Chojnacki J. Envelope protein domains of duck hepatitis B virus: role in assembly and infectivity. [Internet] [Doctoral dissertation]. University of Melbourne; 2005. [cited 2020 Nov 23]. Available from: http://hdl.handle.net/11343/39048.

Council of Science Editors:

Chojnacki J. Envelope protein domains of duck hepatitis B virus: role in assembly and infectivity. [Doctoral Dissertation]. University of Melbourne; 2005. Available from: http://hdl.handle.net/11343/39048

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