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University: University of Alabama – Birmingham

You searched for subject:(Viral proteins). Showing records 1 – 18 of 18 total matches.

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1. Galloway, Summer E. Functional characterization of conserved domains within the L protein component of the vesicular stomatitis virus RNA-dependent RNA polymerase: implications for transcription and MRNA processing.

Degree: PhD, 2008, University of Alabama – Birmingham

Vesicular stomatitis virus (VSV) encodes an RNA-dependent RNA polymerase (RdRp) composed of the 240 kDa large (L) catalytic protein and the phosphoprotein, which replicate the… (more)

Subjects/Keywords: Archaeal Proteins  – chemistry<; br>; Archaeal Proteins  – genetics<; br>; Methyltransferases  – chemistry<; br>; Methyltransferases  – genetics<; br>; RNA Replicase  – chemistry<; br>; RNA Replicase  – genetics<; br>; Viral Proteins  – chemistry<; br>; Viral Proteins  – genetics

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APA (6th Edition):

Galloway, S. E. (2008). Functional characterization of conserved domains within the L protein component of the vesicular stomatitis virus RNA-dependent RNA polymerase: implications for transcription and MRNA processing. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,668

Chicago Manual of Style (16th Edition):

Galloway, Summer E. “Functional characterization of conserved domains within the L protein component of the vesicular stomatitis virus RNA-dependent RNA polymerase: implications for transcription and MRNA processing.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 07, 2020. http://contentdm.mhsl.uab.edu/u?/etd,668.

MLA Handbook (7th Edition):

Galloway, Summer E. “Functional characterization of conserved domains within the L protein component of the vesicular stomatitis virus RNA-dependent RNA polymerase: implications for transcription and MRNA processing.” 2008. Web. 07 Jul 2020.

Vancouver:

Galloway SE. Functional characterization of conserved domains within the L protein component of the vesicular stomatitis virus RNA-dependent RNA polymerase: implications for transcription and MRNA processing. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2020 Jul 07]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,668.

Council of Science Editors:

Galloway SE. Functional characterization of conserved domains within the L protein component of the vesicular stomatitis virus RNA-dependent RNA polymerase: implications for transcription and MRNA processing. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,668

2. Kho, Eun-Young. Is P53 A Target Of Hpv-18 E6 In The Viral Life Cycle?.

Degree: 2012, University of Alabama – Birmingham

The large family of human papillomaviruses (HPVs) infects the cutaneous or mucosal epithelia causing benign hyper proliferative diseases. Infections by the high-risk (HR) HPV genotypes… (more)

Subjects/Keywords: DNA; Viral – metabolism DNA-Binding Proteins – genetics Genes; p53 Human papillomavirus 18 – genetics. Mutation Mutation; Missense Oncogene Proteins; Viral – genetics.

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APA (6th Edition):

Kho, E. (2012). Is P53 A Target Of Hpv-18 E6 In The Viral Life Cycle?. (Thesis). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1730

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):

Kho, Eun-Young. “Is P53 A Target Of Hpv-18 E6 In The Viral Life Cycle?.” 2012. Thesis, University of Alabama – Birmingham. Accessed July 07, 2020. http://contentdm.mhsl.uab.edu/u?/etd,1730.

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

MLA Handbook (7th Edition):

Kho, Eun-Young. “Is P53 A Target Of Hpv-18 E6 In The Viral Life Cycle?.” 2012. Web. 07 Jul 2020.

Vancouver:

Kho E. Is P53 A Target Of Hpv-18 E6 In The Viral Life Cycle?. [Internet] [Thesis]. University of Alabama – Birmingham; 2012. [cited 2020 Jul 07]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1730.

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

Council of Science Editors:

Kho E. Is P53 A Target Of Hpv-18 E6 In The Viral Life Cycle?. [Thesis]. University of Alabama – Birmingham; 2012. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1730

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

3. Indran, Sabarish Vellatheri. Role of the human cytomegalovirus tegument protein pp150 in the trafficking and assembly of infectious virions.

Degree: PhD, 2010, University of Alabama – Birmingham

Human cytomegalovirus, a ubiquitous human pathogen, establishes a persistent infection in the infected host. HCMV assembly takes place in the nucleus and cytoplasm of infected… (more)

Subjects/Keywords: Adaptor Proteins, Signal Transducing – physiology.<; br>; Cytomegalovirus<; br>; Cytoskeletal Proteins – physiology<; br>; Host-Pathogen Interactions.<; br>; Phosphoproteins – metabolism<; br>; Viral Matrix Proteins – metabolism.<; br>; Virus Assembly.<; br>; rab GTP-Binding Proteins – metabolism.

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APA (6th Edition):

Indran, S. V. (2010). Role of the human cytomegalovirus tegument protein pp150 in the trafficking and assembly of infectious virions. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1351

Chicago Manual of Style (16th Edition):

Indran, Sabarish Vellatheri. “Role of the human cytomegalovirus tegument protein pp150 in the trafficking and assembly of infectious virions.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 07, 2020. http://contentdm.mhsl.uab.edu/u?/etd,1351.

MLA Handbook (7th Edition):

Indran, Sabarish Vellatheri. “Role of the human cytomegalovirus tegument protein pp150 in the trafficking and assembly of infectious virions.” 2010. Web. 07 Jul 2020.

Vancouver:

Indran SV. Role of the human cytomegalovirus tegument protein pp150 in the trafficking and assembly of infectious virions. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2020 Jul 07]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1351.

Council of Science Editors:

Indran SV. Role of the human cytomegalovirus tegument protein pp150 in the trafficking and assembly of infectious virions. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1351

4. Krzyzaniak, Magdalena Anna. Role of the gM/gN glycoprotein complex in the final assembly and egress of the human cytomegalovirus (HCMV).

Degree: PhD, 2008, University of Alabama – Birmingham

HCMV consists of a dsDNA genome enclosed by, an icosahedral capsid surrounded by a layer of tegument proteins; the virion structure is enclosed in a… (more)

Subjects/Keywords: Cytomegalovirus  – physiology <; br>; Glycoproteins  – metabolism <; br>; Protein Sorting Signals <; br>; Viral Envelope Proteins  – metabolism <; br>; Virus Assembly <; br>; Virus Replication

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APA (6th Edition):

Krzyzaniak, M. A. (2008). Role of the gM/gN glycoprotein complex in the final assembly and egress of the human cytomegalovirus (HCMV). (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,231

Chicago Manual of Style (16th Edition):

Krzyzaniak, Magdalena Anna. “Role of the gM/gN glycoprotein complex in the final assembly and egress of the human cytomegalovirus (HCMV).” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 07, 2020. http://contentdm.mhsl.uab.edu/u?/etd,231.

MLA Handbook (7th Edition):

Krzyzaniak, Magdalena Anna. “Role of the gM/gN glycoprotein complex in the final assembly and egress of the human cytomegalovirus (HCMV).” 2008. Web. 07 Jul 2020.

Vancouver:

Krzyzaniak MA. Role of the gM/gN glycoprotein complex in the final assembly and egress of the human cytomegalovirus (HCMV). [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2020 Jul 07]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,231.

Council of Science Editors:

Krzyzaniak MA. Role of the gM/gN glycoprotein complex in the final assembly and egress of the human cytomegalovirus (HCMV). [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,231

5. Chang, Jenny Ren-Jye. Scaffolding-mediated capsid size determination in bacteriophages.

Degree: PhD, 2009, University of Alabama – Birmingham

Bacteriophage P2 encodes a scaffolding protein (gpO), which is required for correct assembly of P2 procapsids from the major capsid protein (gpN). The 284-residue gpO… (more)

Subjects/Keywords: Bacteriophages <; br>; DNA viruses <; br>; Scaffold proteins <; br>; Viruses  – Morphology <; br>; Viral genetics <; br>; Staphylococcus aureus.

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APA (6th Edition):

Chang, J. R. (2009). Scaffolding-mediated capsid size determination in bacteriophages. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,562

Chicago Manual of Style (16th Edition):

Chang, Jenny Ren-Jye. “Scaffolding-mediated capsid size determination in bacteriophages.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 07, 2020. http://contentdm.mhsl.uab.edu/u?/etd,562.

MLA Handbook (7th Edition):

Chang, Jenny Ren-Jye. “Scaffolding-mediated capsid size determination in bacteriophages.” 2009. Web. 07 Jul 2020.

Vancouver:

Chang JR. Scaffolding-mediated capsid size determination in bacteriophages. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2020 Jul 07]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,562.

Council of Science Editors:

Chang JR. Scaffolding-mediated capsid size determination in bacteriophages. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,562

6. Odom, Mary Rebecca. Poxvirus evolution: the role of horizontal gene transfer.

Degree: PhD, 2010, University of Alabama – Birmingham

We have investigated the set of all poxvirus proteins for information about the origins of protein coding genes of the Poxviridae family of viruses. A… (more)

Subjects/Keywords: Computational Biology  – methods<; br>; Evolution, Molecular<; br>; Gene Transfer, Horizontal<; br>; Phylogeny<; br>; Poxviridae  – genetics<; br>; Viral Proteins  – genetics

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APA (6th Edition):

Odom, M. R. (2010). Poxvirus evolution: the role of horizontal gene transfer. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,653

Chicago Manual of Style (16th Edition):

Odom, Mary Rebecca. “Poxvirus evolution: the role of horizontal gene transfer.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 07, 2020. http://contentdm.mhsl.uab.edu/u?/etd,653.

MLA Handbook (7th Edition):

Odom, Mary Rebecca. “Poxvirus evolution: the role of horizontal gene transfer.” 2010. Web. 07 Jul 2020.

Vancouver:

Odom MR. Poxvirus evolution: the role of horizontal gene transfer. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2020 Jul 07]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,653.

Council of Science Editors:

Odom MR. Poxvirus evolution: the role of horizontal gene transfer. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,653

7. Carter, Robert J. (Robert Joseph). HPV DNA partitioning during mitosis as followed by fluorescence microscopy.

Degree: PhD, 2010, University of Alabama – Birmingham

Human papillomaviruses (HPVs) are small, double-stranded deoxyribonucleic acid (DNA) tumor viruses capable of establishing persistent infections in the epithelia. After infecting actively-dividing basal cells, the… (more)

Subjects/Keywords: DNA-Binding Proteins<; br>; DNA, Viral  – metabolism<; br>; Microscopy, Fluorescence<; br>; Mitosis<; br>; Papillomaviridae  – metabolism<; br>; Plasmids

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APA (6th Edition):

Carter, R. J. (. J. (2010). HPV DNA partitioning during mitosis as followed by fluorescence microscopy. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1253

Chicago Manual of Style (16th Edition):

Carter, Robert J (Robert Joseph). “HPV DNA partitioning during mitosis as followed by fluorescence microscopy.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 07, 2020. http://contentdm.mhsl.uab.edu/u?/etd,1253.

MLA Handbook (7th Edition):

Carter, Robert J (Robert Joseph). “HPV DNA partitioning during mitosis as followed by fluorescence microscopy.” 2010. Web. 07 Jul 2020.

Vancouver:

Carter RJ(J. HPV DNA partitioning during mitosis as followed by fluorescence microscopy. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2020 Jul 07]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1253.

Council of Science Editors:

Carter RJ(J. HPV DNA partitioning during mitosis as followed by fluorescence microscopy. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1253

8. Genovese, Nicholas J. The mechanism of human papillomavirus E7 protein mediated S-phase reentry in the squamous epithelium.

Degree: PhD, 2010, University of Alabama – Birmingham

Though human papillomavirus infection of the human epidermis is epidemiologically widespread and typically benign, manipulation of the cell cycle within host tissues during infections can… (more)

Subjects/Keywords: Cell Cycle<; br>; Cell Transformation, Viral<; br>; Human papillomavirus 16  – metabolism<; br>; Keratinocytes<; br>; Oncogene Proteins, Viral  – metabolism<; br>; Papillomaviridae  – physiology<; br>; Papillomavirus E7 Proteins  – metabolism<; br>; Receptors, Estrogen  – metabolism<; br>; Retinoblastoma-Like Protein p130  – metabolism<; br>; S Phase

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APA (6th Edition):

Genovese, N. J. (2010). The mechanism of human papillomavirus E7 protein mediated S-phase reentry in the squamous epithelium. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1158

Chicago Manual of Style (16th Edition):

Genovese, Nicholas J. “The mechanism of human papillomavirus E7 protein mediated S-phase reentry in the squamous epithelium.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 07, 2020. http://contentdm.mhsl.uab.edu/u?/etd,1158.

MLA Handbook (7th Edition):

Genovese, Nicholas J. “The mechanism of human papillomavirus E7 protein mediated S-phase reentry in the squamous epithelium.” 2010. Web. 07 Jul 2020.

Vancouver:

Genovese NJ. The mechanism of human papillomavirus E7 protein mediated S-phase reentry in the squamous epithelium. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2020 Jul 07]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1158.

Council of Science Editors:

Genovese NJ. The mechanism of human papillomavirus E7 protein mediated S-phase reentry in the squamous epithelium. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1158

9. Nelson, Michael Paul. Innate Immune Mechanisms Against The Atypical Fungal Pathogen Pneumocystis Murina.

Degree: PhD, 2012, University of Alabama – Birmingham

Pneumonia caused by the fungal pathogen Pneumocystis continues to be the leading cause of morbidity and mortality in AIDS patients. In addition, there are a… (more)

Subjects/Keywords: CD8-Positive T-Lymphocytes – immunology.<; br>; Cell Differentiation – genetics<; br>; Evolution, Molecular.<; br>; Genome, Viral<; br>; HIV Infections<; br>; HIV-1 – immunology<; br>; Immune Evasion.<; br>; Mutation, Missense<; br>; Phenotype<; br>; T-Box Domain Proteins – genetics.<; br>; Viral Proteins – immunology.

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APA (6th Edition):

Nelson, M. P. (2012). Innate Immune Mechanisms Against The Atypical Fungal Pathogen Pneumocystis Murina. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1409

Chicago Manual of Style (16th Edition):

Nelson, Michael Paul. “Innate Immune Mechanisms Against The Atypical Fungal Pathogen Pneumocystis Murina.” 2012. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 07, 2020. http://contentdm.mhsl.uab.edu/u?/etd,1409.

MLA Handbook (7th Edition):

Nelson, Michael Paul. “Innate Immune Mechanisms Against The Atypical Fungal Pathogen Pneumocystis Murina.” 2012. Web. 07 Jul 2020.

Vancouver:

Nelson MP. Innate Immune Mechanisms Against The Atypical Fungal Pathogen Pneumocystis Murina. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2012. [cited 2020 Jul 07]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1409.

Council of Science Editors:

Nelson MP. Innate Immune Mechanisms Against The Atypical Fungal Pathogen Pneumocystis Murina. [Doctoral Dissertation]. University of Alabama – Birmingham; 2012. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1409

10. Yu, Jei-Hwa. MAPKs regulate nuclear import of human papillomavirus type 11 replicative helicase E1.

Degree: PhD, 2008, University of Alabama – Birmingham

Papillomaviruses (PV) are prevalent pathogens that infect human or animal squamous epithelia. Its genome is a double strand circular DNA of approximately 7.9 kb. It… (more)

Subjects/Keywords: DNA Helicases  – metabolism <; br>; DNA-Binding Proteins  – metabolism <; br>; Human papillomavirus 11  – physiology <; br>; Mitogen-Activated Protein Kinases  – metabolism <; br>; Nuclear Localization Signals  – metabolism <; br>; Replication Origin <; br>; Viral Proteins  – metabolism

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APA (6th Edition):

Yu, J. (2008). MAPKs regulate nuclear import of human papillomavirus type 11 replicative helicase E1. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,213

Chicago Manual of Style (16th Edition):

Yu, Jei-Hwa. “MAPKs regulate nuclear import of human papillomavirus type 11 replicative helicase E1.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 07, 2020. http://contentdm.mhsl.uab.edu/u?/etd,213.

MLA Handbook (7th Edition):

Yu, Jei-Hwa. “MAPKs regulate nuclear import of human papillomavirus type 11 replicative helicase E1.” 2008. Web. 07 Jul 2020.

Vancouver:

Yu J. MAPKs regulate nuclear import of human papillomavirus type 11 replicative helicase E1. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2020 Jul 07]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,213.

Council of Science Editors:

Yu J. MAPKs regulate nuclear import of human papillomavirus type 11 replicative helicase E1. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,213

11. Dao, Luan D. Human papillomavirus: segregation and replication.

Degree: PhD, 2008, University of Alabama – Birmingham

Human papillomavirus are small DNA tumor viruses. The viral genome is a small circular double stranded DNA that replicates autonomously as an extrachromosomal plasmid. Occasionally… (more)

Subjects/Keywords: DNA Replication <; br>; DNA-Binding Proteins  – metabolism <; br>; Human papillomavirus 11  – metabolism <; br>; Mitotic Spindle Apparatus  – metabolism <; br>; Replication Origin <; br>; Viral Proteins  – metabolism

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APA (6th Edition):

Dao, L. D. (2008). Human papillomavirus: segregation and replication. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,322

Chicago Manual of Style (16th Edition):

Dao, Luan D. “Human papillomavirus: segregation and replication.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 07, 2020. http://contentdm.mhsl.uab.edu/u?/etd,322.

MLA Handbook (7th Edition):

Dao, Luan D. “Human papillomavirus: segregation and replication.” 2008. Web. 07 Jul 2020.

Vancouver:

Dao LD. Human papillomavirus: segregation and replication. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2020 Jul 07]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,322.

Council of Science Editors:

Dao LD. Human papillomavirus: segregation and replication. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,322

12. 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 07, 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. 07 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 07]. 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

13. Ontiveros, Steven J. Intracellular trafficking of the hantaviral nucleocapsid protein and its function in modulation of immune signaling.

Degree: PhD, 2009, University of Alabama – Birmingham

Old World and New World hantaviruses, family Bunyaviridae, mature intracellularly within cellular compartments. Although it is generally accepted they assemble and bud in the Golgi… (more)

Subjects/Keywords: Apoptosis<; br>; Capsid Proteins  – physiology<; br>; Hantaan virus  – pathogenicity<; br>; Hantavirus  – pathogenicity<; br>; Signal Transduction<; br>; Viral Core Proteins  – physiology<; br>; Virulence Factors  – physiology

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APA (6th Edition):

Ontiveros, S. J. (2009). Intracellular trafficking of the hantaviral nucleocapsid protein and its function in modulation of immune signaling. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,687

Chicago Manual of Style (16th Edition):

Ontiveros, Steven J. “Intracellular trafficking of the hantaviral nucleocapsid protein and its function in modulation of immune signaling.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 07, 2020. http://contentdm.mhsl.uab.edu/u?/etd,687.

MLA Handbook (7th Edition):

Ontiveros, Steven J. “Intracellular trafficking of the hantaviral nucleocapsid protein and its function in modulation of immune signaling.” 2009. Web. 07 Jul 2020.

Vancouver:

Ontiveros SJ. Intracellular trafficking of the hantaviral nucleocapsid protein and its function in modulation of immune signaling. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2020 Jul 07]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,687.

Council of Science Editors:

Ontiveros SJ. Intracellular trafficking of the hantaviral nucleocapsid protein and its function in modulation of immune signaling. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,687

14. Harouaka, Djamila. Investigation of residues of the vesicular stomatitis virus nucleocapsid protein that affect transcription and RNA replication.

Degree: PhD, 2010, University of Alabama – Birmingham

The template for transcription and RNA replication for vesicular stomatitis virus (VSV) and other negative-strand RNA viruses is a ribonucleoprotein (RNP) complex consisting of the… (more)

Subjects/Keywords: Nucleocapsid Proteins  – chemistry<; br>; Nucleocapsid Proteins  – genetics<; br>; Reverse Transcription  – genetics<; br>; RNA, Viral  – genetics<; br>; Vesiculovirus  – genetics<; br>; Vesiculovirus  – physiology<; br>; Virus Replication – genetics

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APA (6th Edition):

Harouaka, D. (2010). Investigation of residues of the vesicular stomatitis virus nucleocapsid protein that affect transcription and RNA replication. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,848

Chicago Manual of Style (16th Edition):

Harouaka, Djamila. “Investigation of residues of the vesicular stomatitis virus nucleocapsid protein that affect transcription and RNA replication.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 07, 2020. http://contentdm.mhsl.uab.edu/u?/etd,848.

MLA Handbook (7th Edition):

Harouaka, Djamila. “Investigation of residues of the vesicular stomatitis virus nucleocapsid protein that affect transcription and RNA replication.” 2010. Web. 07 Jul 2020.

Vancouver:

Harouaka D. Investigation of residues of the vesicular stomatitis virus nucleocapsid protein that affect transcription and RNA replication. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2020 Jul 07]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,848.

Council of Science Editors:

Harouaka D. Investigation of residues of the vesicular stomatitis virus nucleocapsid protein that affect transcription and RNA replication. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,848

15. Murakami, Miho. Fiber modification of adenoviral vectors for cancer gene therapy.

Degree: PhD, 2010, University of Alabama – Birmingham

Cancer still remains a major public health concern despite improvements in primary prevention, early detection and advanced treatments. Cancer gene therapy using human adenovirus serotype… (more)

Subjects/Keywords: Adenoviruses, Human<; br>; Capsid Proteins<; br>; Gene Therapy  – methods<; br>; Genetic Vectors<; br>; Prostatic Neoplasms  – genetics<; br>; Recombinant Fusion Proteins  – metabolism<; br>; Transduction, Genetic<; br>; Viral Tropism  – physiology

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

APA (6th Edition):

Murakami, M. (2010). Fiber modification of adenoviral vectors for cancer gene therapy. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1166

Chicago Manual of Style (16th Edition):

Murakami, Miho. “Fiber modification of adenoviral vectors for cancer gene therapy.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 07, 2020. http://contentdm.mhsl.uab.edu/u?/etd,1166.

MLA Handbook (7th Edition):

Murakami, Miho. “Fiber modification of adenoviral vectors for cancer gene therapy.” 2010. Web. 07 Jul 2020.

Vancouver:

Murakami M. Fiber modification of adenoviral vectors for cancer gene therapy. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2020 Jul 07]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1166.

Council of Science Editors:

Murakami M. Fiber modification of adenoviral vectors for cancer gene therapy. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1166

16. Bhakta, Sushma Jyotika. A functional analysis of the human immunodeficiency virus envelope glycoprotein cytoplasmic domain.

Degree: PhD, 2009, University of Alabama – Birmingham

The retroviral life cycle is separated into two distinct phases of infection. In the first phase, viral enzymes and proteins allow the virus to establish… (more)

Subjects/Keywords: Amino Acid Motifs<; br>; HIV-1  – physiology<; br>; Mutagenesis, Site-Directed<; br>; Viral Fusion Proteins  – metabolism<; br>; Virulence Factors  – metabolism<; br>; Virus Internalization<; br>; env Gene Products, Human Immunodeficiency Virus  – metabolism

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

APA (6th Edition):

Bhakta, S. J. (2009). A functional analysis of the human immunodeficiency virus envelope glycoprotein cytoplasmic domain. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1086

Chicago Manual of Style (16th Edition):

Bhakta, Sushma Jyotika. “A functional analysis of the human immunodeficiency virus envelope glycoprotein cytoplasmic domain.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 07, 2020. http://contentdm.mhsl.uab.edu/u?/etd,1086.

MLA Handbook (7th Edition):

Bhakta, Sushma Jyotika. “A functional analysis of the human immunodeficiency virus envelope glycoprotein cytoplasmic domain.” 2009. Web. 07 Jul 2020.

Vancouver:

Bhakta SJ. A functional analysis of the human immunodeficiency virus envelope glycoprotein cytoplasmic domain. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2020 Jul 07]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1086.

Council of Science Editors:

Bhakta SJ. A functional analysis of the human immunodeficiency virus envelope glycoprotein cytoplasmic domain. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1086

17. Che, Pulin. Identification Of Claudin-1 As An Entry Factor In Dengue Infection And Development Of A High Throughput Screening Assay For Antivirals Against Dengue Virus.

Degree: 2013, University of Alabama – Birmingham

Dengue virus (DENV) has become a huge public health concern around the world with no vaccine or antivirals available. More than one-third of the world's… (more)

Subjects/Keywords: Antiviral Agents<; /br>; Claudin-1 – genetics.<; /br>; Claudin-1 – metabolism.<; /br>; Dengue Virus – physiology.<; /br>; Host-Pathogen Interactions.<; /br>; Protein Interaction Mapping.<; /br>; Viral Proteins – metabolism<; /br>; Virus Internalization.

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

APA (6th Edition):

Che, P. (2013). Identification Of Claudin-1 As An Entry Factor In Dengue Infection And Development Of A High Throughput Screening Assay For Antivirals Against Dengue Virus. (Thesis). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1642

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):

Che, Pulin. “Identification Of Claudin-1 As An Entry Factor In Dengue Infection And Development Of A High Throughput Screening Assay For Antivirals Against Dengue Virus.” 2013. Thesis, University of Alabama – Birmingham. Accessed July 07, 2020. http://contentdm.mhsl.uab.edu/u?/etd,1642.

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

MLA Handbook (7th Edition):

Che, Pulin. “Identification Of Claudin-1 As An Entry Factor In Dengue Infection And Development Of A High Throughput Screening Assay For Antivirals Against Dengue Virus.” 2013. Web. 07 Jul 2020.

Vancouver:

Che P. Identification Of Claudin-1 As An Entry Factor In Dengue Infection And Development Of A High Throughput Screening Assay For Antivirals Against Dengue Virus. [Internet] [Thesis]. University of Alabama – Birmingham; 2013. [cited 2020 Jul 07]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1642.

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

Council of Science Editors:

Che P. Identification Of Claudin-1 As An Entry Factor In Dengue Infection And Development Of A High Throughput Screening Assay For Antivirals Against Dengue Virus. [Thesis]. University of Alabama – Birmingham; 2013. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1642

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

18. Cox, Robert Marsden. Characterization Of The Mumps Virus Replicase.

Degree: 2013, University of Alabama – Birmingham

Negative strand RNA viruses (NSV) are unique because their nucleocapsids are used directly as the template for both transcription and replication. The viral genomic RNA… (more)

Subjects/Keywords: Models, Molecular<; /br>; Mumps virus – genetics.<; /br>; Mumps virus – metabolism.<; /br>; Nucleocapsid<; /br>; Nucleocapsid Proteins – metabolism.<; /br>; Phosphoproteins<; /br>; Protein Conformation<; /br>; RNA, Viral<; /br>; Virion

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

APA (6th Edition):

Cox, R. M. (2013). Characterization Of The Mumps Virus Replicase. (Thesis). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1666

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):

Cox, Robert Marsden. “Characterization Of The Mumps Virus Replicase.” 2013. Thesis, University of Alabama – Birmingham. Accessed July 07, 2020. http://contentdm.mhsl.uab.edu/u?/etd,1666.

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

MLA Handbook (7th Edition):

Cox, Robert Marsden. “Characterization Of The Mumps Virus Replicase.” 2013. Web. 07 Jul 2020.

Vancouver:

Cox RM. Characterization Of The Mumps Virus Replicase. [Internet] [Thesis]. University of Alabama – Birmingham; 2013. [cited 2020 Jul 07]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1666.

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

Council of Science Editors:

Cox RM. Characterization Of The Mumps Virus Replicase. [Thesis]. University of Alabama – Birmingham; 2013. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1666

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

.