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Level: masters

You searched for subject:(Viral proteins). Showing records 1 – 11 of 11 total matches.

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Oregon State University

1. Blouch, Robert Edward. Disulphide bond formation is essential for vaccinia virus late protein L1R function and for production of infectious progeny.

Degree: MS, Microbiology, 2005, Oregon State University

 L1R, a myristylated late gene product of vaccinia virus, is essential for formation of infectious intracellular mature virions (IMV). In its absence, only viral particles… (more)

Subjects/Keywords: Viral proteins

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APA (6th Edition):

Blouch, R. E. (2005). Disulphide bond formation is essential for vaccinia virus late protein L1R function and for production of infectious progeny. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/22927

Chicago Manual of Style (16th Edition):

Blouch, Robert Edward. “Disulphide bond formation is essential for vaccinia virus late protein L1R function and for production of infectious progeny.” 2005. Masters Thesis, Oregon State University. Accessed July 02, 2020. http://hdl.handle.net/1957/22927.

MLA Handbook (7th Edition):

Blouch, Robert Edward. “Disulphide bond formation is essential for vaccinia virus late protein L1R function and for production of infectious progeny.” 2005. Web. 02 Jul 2020.

Vancouver:

Blouch RE. Disulphide bond formation is essential for vaccinia virus late protein L1R function and for production of infectious progeny. [Internet] [Masters thesis]. Oregon State University; 2005. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1957/22927.

Council of Science Editors:

Blouch RE. Disulphide bond formation is essential for vaccinia virus late protein L1R function and for production of infectious progeny. [Masters Thesis]. Oregon State University; 2005. Available from: http://hdl.handle.net/1957/22927


McGill University

2. Ricciardi, Riccardo Pietro, 1985-. A role for high-risk HPV type 16 E6 and E7 oncoproteins in colorecteral carcinogenesis.

Degree: MS, Division of Experimental Medicine., 2007, McGill University

 Human papillomavirus (HPV) infections play a crucial role in human carcinogenesis. Greater than 96% of all cervical carcinomas are positive for high-risk HPV infections; especially… (more)

Subjects/Keywords: Colorectal Neoplasms  – etiology.; Oncogene Proteins, Viral.

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APA (6th Edition):

Ricciardi, Riccardo Pietro, 1. (2007). A role for high-risk HPV type 16 E6 and E7 oncoproteins in colorecteral carcinogenesis. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile112351.pdf

Chicago Manual of Style (16th Edition):

Ricciardi, Riccardo Pietro, 1985-. “A role for high-risk HPV type 16 E6 and E7 oncoproteins in colorecteral carcinogenesis.” 2007. Masters Thesis, McGill University. Accessed July 02, 2020. http://digitool.library.mcgill.ca/thesisfile112351.pdf.

MLA Handbook (7th Edition):

Ricciardi, Riccardo Pietro, 1985-. “A role for high-risk HPV type 16 E6 and E7 oncoproteins in colorecteral carcinogenesis.” 2007. Web. 02 Jul 2020.

Vancouver:

Ricciardi, Riccardo Pietro 1. A role for high-risk HPV type 16 E6 and E7 oncoproteins in colorecteral carcinogenesis. [Internet] [Masters thesis]. McGill University; 2007. [cited 2020 Jul 02]. Available from: http://digitool.library.mcgill.ca/thesisfile112351.pdf.

Council of Science Editors:

Ricciardi, Riccardo Pietro 1. A role for high-risk HPV type 16 E6 and E7 oncoproteins in colorecteral carcinogenesis. [Masters Thesis]. McGill University; 2007. Available from: http://digitool.library.mcgill.ca/thesisfile112351.pdf


University of Toronto

3. Elion-Jourard, Shira S. Syncytins and cell fusion in the placenta: Structural insights into lipid membrane fusion and placental development.

Degree: 2018, University of Toronto

Endogenous retroviruses (ERV) are genetic elements found in eukaryotes of retroviral origin. Despite making up a substantial portion of vertebrate genomes, very few ERV genes… (more)

Subjects/Keywords: Fusion Proteins; Placental Development; Structural Biology; Syncytin; Viral Fusion; X-Ray Crystallography; 0487

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APA (6th Edition):

Elion-Jourard, S. S. (2018). Syncytins and cell fusion in the placenta: Structural insights into lipid membrane fusion and placental development. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/91500

Chicago Manual of Style (16th Edition):

Elion-Jourard, Shira S. “Syncytins and cell fusion in the placenta: Structural insights into lipid membrane fusion and placental development.” 2018. Masters Thesis, University of Toronto. Accessed July 02, 2020. http://hdl.handle.net/1807/91500.

MLA Handbook (7th Edition):

Elion-Jourard, Shira S. “Syncytins and cell fusion in the placenta: Structural insights into lipid membrane fusion and placental development.” 2018. Web. 02 Jul 2020.

Vancouver:

Elion-Jourard SS. Syncytins and cell fusion in the placenta: Structural insights into lipid membrane fusion and placental development. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1807/91500.

Council of Science Editors:

Elion-Jourard SS. Syncytins and cell fusion in the placenta: Structural insights into lipid membrane fusion and placental development. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/91500


McGill University

4. Ainsworth, Julia. Comparison of p53 and MAGI-3 regulation mediated by the E6 protein from high-risk human papillomavirus types 18 and 33.

Degree: MS, Department of Microbiology and Immunology., 2007, McGill University

The HPV E6-p53 interaction is well-understood, but not for all high-risk HPV types. In addition, HPV E6 p53-independent functions are gaining recognition for their importance… (more)

Subjects/Keywords: Viral Envelope Proteins  – metabolism.; Oncogene Proteins, Viral  – metabolism.; Papillomaviridae  – physiology.; Tumor Suppressor Protein p53  – metabolism.; Membrane Proteins  – metabolism.

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APA (6th Edition):

Ainsworth, J. (2007). Comparison of p53 and MAGI-3 regulation mediated by the E6 protein from high-risk human papillomavirus types 18 and 33. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile112368.pdf

Chicago Manual of Style (16th Edition):

Ainsworth, Julia. “Comparison of p53 and MAGI-3 regulation mediated by the E6 protein from high-risk human papillomavirus types 18 and 33.” 2007. Masters Thesis, McGill University. Accessed July 02, 2020. http://digitool.library.mcgill.ca/thesisfile112368.pdf.

MLA Handbook (7th Edition):

Ainsworth, Julia. “Comparison of p53 and MAGI-3 regulation mediated by the E6 protein from high-risk human papillomavirus types 18 and 33.” 2007. Web. 02 Jul 2020.

Vancouver:

Ainsworth J. Comparison of p53 and MAGI-3 regulation mediated by the E6 protein from high-risk human papillomavirus types 18 and 33. [Internet] [Masters thesis]. McGill University; 2007. [cited 2020 Jul 02]. Available from: http://digitool.library.mcgill.ca/thesisfile112368.pdf.

Council of Science Editors:

Ainsworth J. Comparison of p53 and MAGI-3 regulation mediated by the E6 protein from high-risk human papillomavirus types 18 and 33. [Masters Thesis]. McGill University; 2007. Available from: http://digitool.library.mcgill.ca/thesisfile112368.pdf


Rockefeller University

5. Murray, Catherine Lucy. Genetic and Biochemical Analyses of the Flaviviridae Capsid Proteins.

Degree: 2007, Rockefeller University

  The small, enveloped viruses of the family Flaviviridae are etiological agents of numerous important human and agricultural diseases including hepatitis C, yellow fever, and… (more)

Subjects/Keywords: flaviviridae; viral capsid proteins; hepatitis c virus; infectious particle assembly; Life Sciences

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APA (6th Edition):

Murray, C. L. (2007). Genetic and Biochemical Analyses of the Flaviviridae Capsid Proteins. (Masters Thesis). Rockefeller University. Retrieved from https://digitalcommons.rockefeller.edu/student_theses_and_dissertations/24

Chicago Manual of Style (16th Edition):

Murray, Catherine Lucy. “Genetic and Biochemical Analyses of the Flaviviridae Capsid Proteins.” 2007. Masters Thesis, Rockefeller University. Accessed July 02, 2020. https://digitalcommons.rockefeller.edu/student_theses_and_dissertations/24.

MLA Handbook (7th Edition):

Murray, Catherine Lucy. “Genetic and Biochemical Analyses of the Flaviviridae Capsid Proteins.” 2007. Web. 02 Jul 2020.

Vancouver:

Murray CL. Genetic and Biochemical Analyses of the Flaviviridae Capsid Proteins. [Internet] [Masters thesis]. Rockefeller University; 2007. [cited 2020 Jul 02]. Available from: https://digitalcommons.rockefeller.edu/student_theses_and_dissertations/24.

Council of Science Editors:

Murray CL. Genetic and Biochemical Analyses of the Flaviviridae Capsid Proteins. [Masters Thesis]. Rockefeller University; 2007. Available from: https://digitalcommons.rockefeller.edu/student_theses_and_dissertations/24

6. Marion, William R. (William Robert). Bacteriophage P22 scaffolding protein : functions and mechanisms in procapsid assembly.

Degree: MS, 2007, University of Alabama – Birmingham

Bacteriophage P22 scaffolding protein is responsible for controlling the assembly of 420 monomeric coat protein subunits into a spherical, T=7 procapsid lattice. The precise mechanism… (more)

Subjects/Keywords: Bacteriophage P22  – growth & development<; br>; Bacteriophage P22  – chemistry<; br>; Bacteriophage P22  – genetics<; br>; Capsid Proteins  – chemistry<; br>; Models, Molecular<; br>; Viral Structural Proteins  – physiology

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APA (6th Edition):

Marion, W. R. (. R. (2007). Bacteriophage P22 scaffolding protein : functions and mechanisms in procapsid assembly. (Masters Thesis). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,455

Chicago Manual of Style (16th Edition):

Marion, William R (William Robert). “Bacteriophage P22 scaffolding protein : functions and mechanisms in procapsid assembly.” 2007. Masters Thesis, University of Alabama – Birmingham. Accessed July 02, 2020. http://contentdm.mhsl.uab.edu/u?/etd,455.

MLA Handbook (7th Edition):

Marion, William R (William Robert). “Bacteriophage P22 scaffolding protein : functions and mechanisms in procapsid assembly.” 2007. Web. 02 Jul 2020.

Vancouver:

Marion WR(R. Bacteriophage P22 scaffolding protein : functions and mechanisms in procapsid assembly. [Internet] [Masters thesis]. University of Alabama – Birmingham; 2007. [cited 2020 Jul 02]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,455.

Council of Science Editors:

Marion WR(R. Bacteriophage P22 scaffolding protein : functions and mechanisms in procapsid assembly. [Masters Thesis]. University of Alabama – Birmingham; 2007. Available from: http://contentdm.mhsl.uab.edu/u?/etd,455


University of Utah

7. Liang, Lingming. Cloning of the E1M gene of human papillomavirus type 16 and production of an antibody to the E1M protein;.

Degree: MS;, Pathology;, 1990, University of Utah

 Since the DNA of human papillomaviruses (HPV) can be found in at least 90% of cervical cancers, it has been implicated that HPV may be… (more)

Subjects/Keywords: Immunology; Genetics; Etiology; Gene Expression Regulation; Immune Sera$xbiosynthesis; Immunogenetics; Papillomavirus, Human; Rabbits; Recombinant Fusion Proteins; Viral Fusion Proteins

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APA (6th Edition):

Liang, L. (1990). Cloning of the E1M gene of human papillomavirus type 16 and production of an antibody to the E1M protein;. (Masters Thesis). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/122/rec/171

Chicago Manual of Style (16th Edition):

Liang, Lingming. “Cloning of the E1M gene of human papillomavirus type 16 and production of an antibody to the E1M protein;.” 1990. Masters Thesis, University of Utah. Accessed July 02, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/122/rec/171.

MLA Handbook (7th Edition):

Liang, Lingming. “Cloning of the E1M gene of human papillomavirus type 16 and production of an antibody to the E1M protein;.” 1990. Web. 02 Jul 2020.

Vancouver:

Liang L. Cloning of the E1M gene of human papillomavirus type 16 and production of an antibody to the E1M protein;. [Internet] [Masters thesis]. University of Utah; 1990. [cited 2020 Jul 02]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/122/rec/171.

Council of Science Editors:

Liang L. Cloning of the E1M gene of human papillomavirus type 16 and production of an antibody to the E1M protein;. [Masters Thesis]. University of Utah; 1990. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/122/rec/171

8. Varela, Queli Defaveri. Uso de sistemas virais citoplasmáticos de Saccharomyces cerevisiae para a produção de proteínas heterólogas.

Degree: 2008, Universidade de Caxias do Sul

A produção de proteínas e peptídeos heterólogos representa um dos mais importantes segmentos do setor biotecnológico. Apesar das diferentes tecnologias hoje disponíveis para a (bio)… (more)

Subjects/Keywords: Ciências da Saúde; Saccharomyces cerevisiae; Sistemas virais; Proteínas heterólogas; Vírus X; Saccharomyces cerevisiae; Viral systems; Heterologous proteins; Virus X

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APA (6th Edition):

Varela, Q. D. (2008). Uso de sistemas virais citoplasmáticos de Saccharomyces cerevisiae para a produção de proteínas heterólogas. (Masters Thesis). Universidade de Caxias do Sul. Retrieved from https://repositorio.ucs.br/handle/11338/531

Chicago Manual of Style (16th Edition):

Varela, Queli Defaveri. “Uso de sistemas virais citoplasmáticos de Saccharomyces cerevisiae para a produção de proteínas heterólogas.” 2008. Masters Thesis, Universidade de Caxias do Sul. Accessed July 02, 2020. https://repositorio.ucs.br/handle/11338/531.

MLA Handbook (7th Edition):

Varela, Queli Defaveri. “Uso de sistemas virais citoplasmáticos de Saccharomyces cerevisiae para a produção de proteínas heterólogas.” 2008. Web. 02 Jul 2020.

Vancouver:

Varela QD. Uso de sistemas virais citoplasmáticos de Saccharomyces cerevisiae para a produção de proteínas heterólogas. [Internet] [Masters thesis]. Universidade de Caxias do Sul; 2008. [cited 2020 Jul 02]. Available from: https://repositorio.ucs.br/handle/11338/531.

Council of Science Editors:

Varela QD. Uso de sistemas virais citoplasmáticos de Saccharomyces cerevisiae para a produção de proteínas heterólogas. [Masters Thesis]. Universidade de Caxias do Sul; 2008. Available from: https://repositorio.ucs.br/handle/11338/531

9. Weeks, Anastasia C. Structural and functional analysis of the Vaccinia virus O1 virulence protein.

Degree: MS, MS-Biomedical Science, 2017, East Carolina University

 Poxviruses are double-stranded DNA viruses capable of causing disfiguring and deadly disease in a wide range of hosts, from insects to mammals. Orthopoxviruses (OPXV) encode… (more)

Subjects/Keywords: poxvirus; O1L; mutant; immune; attenuated; plaque; morphology; cell; migration; Virulence; Viral Proteins; Vaccinia virus

…single lipid bilayer studded with non-glycosylated viral proteins (2). The other… …additional viral membrane containing an alternate set of glycosylated viral and host proteins… …with at least 12 separate viral proteins forming a complex to facilitate fusion independently… …is released into the cytoplasm. Microtubule machinery is hijacked by viral proteins to… …intermediate, and late. Prior to viral DNA replication, early genes are expressed to produce proteins… 

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APA (6th Edition):

Weeks, A. C. (2017). Structural and functional analysis of the Vaccinia virus O1 virulence protein. (Masters Thesis). East Carolina University. Retrieved from http://hdl.handle.net/10342/6393

Chicago Manual of Style (16th Edition):

Weeks, Anastasia C. “Structural and functional analysis of the Vaccinia virus O1 virulence protein.” 2017. Masters Thesis, East Carolina University. Accessed July 02, 2020. http://hdl.handle.net/10342/6393.

MLA Handbook (7th Edition):

Weeks, Anastasia C. “Structural and functional analysis of the Vaccinia virus O1 virulence protein.” 2017. Web. 02 Jul 2020.

Vancouver:

Weeks AC. Structural and functional analysis of the Vaccinia virus O1 virulence protein. [Internet] [Masters thesis]. East Carolina University; 2017. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/10342/6393.

Council of Science Editors:

Weeks AC. Structural and functional analysis of the Vaccinia virus O1 virulence protein. [Masters Thesis]. East Carolina University; 2017. Available from: http://hdl.handle.net/10342/6393

10. Singh, Jasleen. Characterization of Self-Interaction of Arabidopsis thaliana Double-Stranded RNA Binding Protein 4.

Degree: MS, Plant Pathology, 2012, The Ohio State University

 The interaction between Arabidopsis thaliana double stranded RNA binding protein 4 (DRB4) and dicer-like 4 (DCL4) has been shown to be necessary for RNA silencing.… (more)

Subjects/Keywords: Biology; Molecular Biology; Plant Biology; Plant Pathology; Plant Sciences; RNA silencing; anti-viral defense; double stranded RNA binding proteins; DRB4

…9 vii 2.2.2- AGO proteins: the catalytic core of RNA silencing… …15 2.2.4- Double- stranded RNA binding proteins (DRBs): friends with dicers… …4 Figure 2: Domain structure of AGO family proteins… …13 Figure 3: Schematic drawings of five double-stranded RNA binding proteins in Arabidopsis… …63 Figure 15: Graphs showing the OD410 values of various combinations of proteins tested… 

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APA (6th Edition):

Singh, J. (2012). Characterization of Self-Interaction of Arabidopsis thaliana Double-Stranded RNA Binding Protein 4. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1337822686

Chicago Manual of Style (16th Edition):

Singh, Jasleen. “Characterization of Self-Interaction of Arabidopsis thaliana Double-Stranded RNA Binding Protein 4.” 2012. Masters Thesis, The Ohio State University. Accessed July 02, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1337822686.

MLA Handbook (7th Edition):

Singh, Jasleen. “Characterization of Self-Interaction of Arabidopsis thaliana Double-Stranded RNA Binding Protein 4.” 2012. Web. 02 Jul 2020.

Vancouver:

Singh J. Characterization of Self-Interaction of Arabidopsis thaliana Double-Stranded RNA Binding Protein 4. [Internet] [Masters thesis]. The Ohio State University; 2012. [cited 2020 Jul 02]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1337822686.

Council of Science Editors:

Singh J. Characterization of Self-Interaction of Arabidopsis thaliana Double-Stranded RNA Binding Protein 4. [Masters Thesis]. The Ohio State University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1337822686

11. Malta, Fernanda de Mello. "Sequenciamento da região NS5A do genoma do vírus da hepatite C, genótipo 3, de pacientes brasileiros com infecção crônica".

Degree: Mestrado, Fisiopatologia Experimental, 2006, University of São Paulo

No presente estudo, foram selecionados 33 pacientes infectados com HCV genótipo 3a, tratados com IFN e Ribavirina, incluindo pacientes cirróticos (C) e não-cirróticos (NC), respondedores… (more)

Subjects/Keywords: Análise mutacional do DNA; Chronic hepatitis C; DNA mutational analyses; EIF-2 kinase; Genótipo; Genotype; Hepatite C crônica; IEF-2 kinase; Interferon alfa; Interferon-alpha; Proteínas não estruturais virais; Viral nonstrutural proteins

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APA (6th Edition):

Malta, F. d. M. (2006). "Sequenciamento da região NS5A do genoma do vírus da hepatite C, genótipo 3, de pacientes brasileiros com infecção crônica". (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5160/tde-17102006-120049/ ;

Chicago Manual of Style (16th Edition):

Malta, Fernanda de Mello. “"Sequenciamento da região NS5A do genoma do vírus da hepatite C, genótipo 3, de pacientes brasileiros com infecção crônica".” 2006. Masters Thesis, University of São Paulo. Accessed July 02, 2020. http://www.teses.usp.br/teses/disponiveis/5/5160/tde-17102006-120049/ ;.

MLA Handbook (7th Edition):

Malta, Fernanda de Mello. “"Sequenciamento da região NS5A do genoma do vírus da hepatite C, genótipo 3, de pacientes brasileiros com infecção crônica".” 2006. Web. 02 Jul 2020.

Vancouver:

Malta FdM. "Sequenciamento da região NS5A do genoma do vírus da hepatite C, genótipo 3, de pacientes brasileiros com infecção crônica". [Internet] [Masters thesis]. University of São Paulo; 2006. [cited 2020 Jul 02]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-17102006-120049/ ;.

Council of Science Editors:

Malta FdM. "Sequenciamento da região NS5A do genoma do vírus da hepatite C, genótipo 3, de pacientes brasileiros com infecção crônica". [Masters Thesis]. University of São Paulo; 2006. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-17102006-120049/ ;

.