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You searched for +publisher:"University of Alabama – Birmingham" +contributor:("Sztul, Elizabeth S."). Showing records 1 – 11 of 11 total matches.

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1. 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 November 11, 2019. 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. 11 Nov 2019.

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 2019 Nov 11]. 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

2. Jurkuvenaite, Asta. Biogenesis, trafficking, and function of wild-type and mutant cystic fibrosis transmembrane conductance regulator (CFTR).

Degree: PhD, 2008, University of Alabama – Birmingham

Cystic fibrosis (CF) is a genetic disease resulting from mutations in the cystic fibrosis transmembrane conductance regulator (CFTR), a cAMP-activated chloride channel that functions at… (more)

Subjects/Keywords: Biotinylation. Cell Membrane  – metabolism<; br>; Cystic Fibrosis Transmembrane Conductance Regulator  – chemistry<; br>; Cystic Fibrosis Transmembrane Conductance Regulator  – metabolism<; br>; Mutation<; br>; Protein Structure, Tertiary

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APA (6th Edition):

Jurkuvenaite, A. (2008). Biogenesis, trafficking, and function of wild-type and mutant cystic fibrosis transmembrane conductance regulator (CFTR). (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,601

Chicago Manual of Style (16th Edition):

Jurkuvenaite, Asta. “Biogenesis, trafficking, and function of wild-type and mutant cystic fibrosis transmembrane conductance regulator (CFTR).” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed November 11, 2019. http://contentdm.mhsl.uab.edu/u?/etd,601.

MLA Handbook (7th Edition):

Jurkuvenaite, Asta. “Biogenesis, trafficking, and function of wild-type and mutant cystic fibrosis transmembrane conductance regulator (CFTR).” 2008. Web. 11 Nov 2019.

Vancouver:

Jurkuvenaite A. Biogenesis, trafficking, and function of wild-type and mutant cystic fibrosis transmembrane conductance regulator (CFTR). [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2019 Nov 11]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,601.

Council of Science Editors:

Jurkuvenaite A. Biogenesis, trafficking, and function of wild-type and mutant cystic fibrosis transmembrane conductance regulator (CFTR). [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,601

3. Tower-Gilchrist, Cristy (Cristy Davette). The role of protein folding and protein trafficking in human disease.

Degree: PhD, 2011, University of Alabama – Birmingham

Project 1: Expansion of CAG repeats encoding glutamine in huntingtin and ataxin 3 causes the neurodegenerative diseases Huntington's disease (HD) and spinocerebellar ataxia 3 (SCA3),… (more)

Subjects/Keywords: Cilia<; br>; Cytomegalovirus  – enzymology<; br>; Huntington Disease  – virology<; br>; Neurons  – metabolism<; br>; Peptides  – antagonists & inhibitors<; br>; Phosphotransferases (Alcohol Group Acceptor)  – physiology<; br>; Spinocerebellar Ataxias  – virology

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APA (6th Edition):

Tower-Gilchrist, C. (. D. (2011). The role of protein folding and protein trafficking in human disease. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,964

Chicago Manual of Style (16th Edition):

Tower-Gilchrist, Cristy (Cristy Davette). “The role of protein folding and protein trafficking in human disease.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed November 11, 2019. http://contentdm.mhsl.uab.edu/u?/etd,964.

MLA Handbook (7th Edition):

Tower-Gilchrist, Cristy (Cristy Davette). “The role of protein folding and protein trafficking in human disease.” 2011. Web. 11 Nov 2019.

Vancouver:

Tower-Gilchrist C(D. The role of protein folding and protein trafficking in human disease. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2019 Nov 11]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,964.

Council of Science Editors:

Tower-Gilchrist C(D. The role of protein folding and protein trafficking in human disease. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,964

4. Ramanathan, Harish N. Trafficking of hantaviral nucleocapsid proteins.

Degree: PhD, 2007, University of Alabama – Birmingham

 Hantaviruses are enveloped, negative-sense RNA viruses belonging to genus Hantavirus, within the family Bunyaviridae. Hantaviruses include many serious human pathogens and are classified as Old… (more)

Subjects/Keywords: Hantavirus  – drug effects <; br>; Hantavirus  – genetics <; br>; Hantavirus  – metabolism <; br>; Nucleosides  – chemical synthesis <; br>; Nucleosides  – metabolism

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APA (6th Edition):

Ramanathan, H. N. (2007). Trafficking of hantaviral nucleocapsid proteins. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,261

Chicago Manual of Style (16th Edition):

Ramanathan, Harish N. “Trafficking of hantaviral nucleocapsid proteins.” 2007. Doctoral Dissertation, University of Alabama – Birmingham. Accessed November 11, 2019. http://contentdm.mhsl.uab.edu/u?/etd,261.

MLA Handbook (7th Edition):

Ramanathan, Harish N. “Trafficking of hantaviral nucleocapsid proteins.” 2007. Web. 11 Nov 2019.

Vancouver:

Ramanathan HN. Trafficking of hantaviral nucleocapsid proteins. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2007. [cited 2019 Nov 11]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,261.

Council of Science Editors:

Ramanathan HN. Trafficking of hantaviral nucleocapsid proteins. [Doctoral Dissertation]. University of Alabama – Birmingham; 2007. Available from: http://contentdm.mhsl.uab.edu/u?/etd,261

5. Williams, Corey L. Analysis of cystic kidney disease-related genes in Caenorhabditis elegans.

Degree: PhD, 2009, University of Alabama – Birmingham

Cilia are evolutionarily conserved, membrane-bound, microtubule-based organelles found on a diverse array of cell types in eukaryotic organisms. Inherited diseases of cilia protein dysfunction include… (more)

Subjects/Keywords: Caenorhabditis elegans  – cytology<; br>; Caenorhabditis elegans  – metabolism<; br>; Caenorhabditis elegans Proteins  – metabolism<; br>; Cilia  – metabolism<; br>; Protein Transport

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APA (6th Edition):

Williams, C. L. (2009). Analysis of cystic kidney disease-related genes in Caenorhabditis elegans. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,407

Chicago Manual of Style (16th Edition):

Williams, Corey L. “Analysis of cystic kidney disease-related genes in Caenorhabditis elegans.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed November 11, 2019. http://contentdm.mhsl.uab.edu/u?/etd,407.

MLA Handbook (7th Edition):

Williams, Corey L. “Analysis of cystic kidney disease-related genes in Caenorhabditis elegans.” 2009. Web. 11 Nov 2019.

Vancouver:

Williams CL. Analysis of cystic kidney disease-related genes in Caenorhabditis elegans. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Nov 11]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,407.

Council of Science Editors:

Williams CL. Analysis of cystic kidney disease-related genes in Caenorhabditis elegans. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,407

6. Ding, Huiping. Regulation of tau functions by posttranslational modifications of tau and histone deacetylase 6.

Degree: PhD, 2008, University of Alabama – Birmingham

Alzheimer’s disease (AD), the most common neurodegenerative disease, is pathologically characterized by senile plaques composed of amyloid [beta] peptide and neurofibrillary tangles composed of hyperphosphorylated… (more)

Subjects/Keywords: Alzheimer Disease  – metabolism<; br>; Brain  – metabolism<; br>; Caspases  – metabolism<; br>; Histone Deacetylases  – metabolism<; br>; Microtubules  – metabolism<; br>; Neurons  – metabolism<; br>; tau Proteins  – metabolism

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APA (6th Edition):

Ding, H. (2008). Regulation of tau functions by posttranslational modifications of tau and histone deacetylase 6. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,439

Chicago Manual of Style (16th Edition):

Ding, Huiping. “Regulation of tau functions by posttranslational modifications of tau and histone deacetylase 6.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed November 11, 2019. http://contentdm.mhsl.uab.edu/u?/etd,439.

MLA Handbook (7th Edition):

Ding, Huiping. “Regulation of tau functions by posttranslational modifications of tau and histone deacetylase 6.” 2008. Web. 11 Nov 2019.

Vancouver:

Ding H. Regulation of tau functions by posttranslational modifications of tau and histone deacetylase 6. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2019 Nov 11]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,439.

Council of Science Editors:

Ding H. Regulation of tau functions by posttranslational modifications of tau and histone deacetylase 6. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,439

7. Parish, Lindsay A. Protein trafficking and 4.1R relocalization in Plasmodium falciparum-infected erythrocytes.

Degree: PhD, 2009, University of Alabama – Birmingham

Malaria is a mosquito-borne infectious disease that is caused by parasites in the genus Plasmodium. There are four species of malaria that routinely infect humans,… (more)

Subjects/Keywords: Erythrocytes  – metabolism<; br>; Plasmodium falciparum  – metabolism<; br>; Protozoan Proteins  – genetics<; br>; Qa-SNARE Proteins  – genetics<; br>; Secretory Pathway  – genetics

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APA (6th Edition):

Parish, L. A. (2009). Protein trafficking and 4.1R relocalization in Plasmodium falciparum-infected erythrocytes. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,503

Chicago Manual of Style (16th Edition):

Parish, Lindsay A. “Protein trafficking and 4.1R relocalization in Plasmodium falciparum-infected erythrocytes.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed November 11, 2019. http://contentdm.mhsl.uab.edu/u?/etd,503.

MLA Handbook (7th Edition):

Parish, Lindsay A. “Protein trafficking and 4.1R relocalization in Plasmodium falciparum-infected erythrocytes.” 2009. Web. 11 Nov 2019.

Vancouver:

Parish LA. Protein trafficking and 4.1R relocalization in Plasmodium falciparum-infected erythrocytes. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Nov 11]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,503.

Council of Science Editors:

Parish LA. Protein trafficking and 4.1R relocalization in Plasmodium falciparum-infected erythrocytes. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,503

8. Matthews, Tori A. Pathological modifications of tau induce toxicity and facilitate cell death.

Degree: PhD, 2009, University of Alabama – Birmingham

lzheimer’s disease (AD) is a progressive neurodegenerative disorder characterized by two major pathophysiological hallmarks, beta-amyloid (A[Beta]) plaques and tau tangles. In AD and other tau… (more)

Subjects/Keywords: Caspases  – metabolism<; br>; Cell Death  – physiology<; br>; Microtubules  – metabolism<; br>; tau Proteins  – physiology

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APA (6th Edition):

Matthews, T. A. (2009). Pathological modifications of tau induce toxicity and facilitate cell death. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,607

Chicago Manual of Style (16th Edition):

Matthews, Tori A. “Pathological modifications of tau induce toxicity and facilitate cell death.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed November 11, 2019. http://contentdm.mhsl.uab.edu/u?/etd,607.

MLA Handbook (7th Edition):

Matthews, Tori A. “Pathological modifications of tau induce toxicity and facilitate cell death.” 2009. Web. 11 Nov 2019.

Vancouver:

Matthews TA. Pathological modifications of tau induce toxicity and facilitate cell death. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Nov 11]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,607.

Council of Science Editors:

Matthews TA. Pathological modifications of tau induce toxicity and facilitate cell death. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,607

9. Winkelbauer, Marlene Elizabeth. Elucidating the role of nephronophthisis proteins utilizing Caenorhabditis elegans as a model.

Degree: PhD, 2007, University of Alabama – Birmingham

Numerous disorders are characterized by the presence of cystic lesions within the kidney. The proteins associated with these disorders often localize to cilia, and improper… (more)

Subjects/Keywords: Caenorhabditis elegans  – genetics<; br>; Caenorhabditis elegans Proteins  – genetics<; br>; Cilia  – metabolism<; br>; Neurons, Afferent  – physiology<; br>; Protein Transport<; br>; Transcription Factors  – metabolism

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APA (6th Edition):

Winkelbauer, M. E. (2007). Elucidating the role of nephronophthisis proteins utilizing Caenorhabditis elegans as a model. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,619

Chicago Manual of Style (16th Edition):

Winkelbauer, Marlene Elizabeth. “Elucidating the role of nephronophthisis proteins utilizing Caenorhabditis elegans as a model.” 2007. Doctoral Dissertation, University of Alabama – Birmingham. Accessed November 11, 2019. http://contentdm.mhsl.uab.edu/u?/etd,619.

MLA Handbook (7th Edition):

Winkelbauer, Marlene Elizabeth. “Elucidating the role of nephronophthisis proteins utilizing Caenorhabditis elegans as a model.” 2007. Web. 11 Nov 2019.

Vancouver:

Winkelbauer ME. Elucidating the role of nephronophthisis proteins utilizing Caenorhabditis elegans as a model. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2007. [cited 2019 Nov 11]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,619.

Council of Science Editors:

Winkelbauer ME. Elucidating the role of nephronophthisis proteins utilizing Caenorhabditis elegans as a model. [Doctoral Dissertation]. University of Alabama – Birmingham; 2007. Available from: http://contentdm.mhsl.uab.edu/u?/etd,619

10. 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 November 11, 2019. 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. 11 Nov 2019.

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 2019 Nov 11]. 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

11. Gill, Rachel B. Human cytomegalovirus UL97 kinase activity modifies cell cycle checkpoint regulators.

Degree: PhD, 2011, University of Alabama – Birmingham

Human cytomegalovirus (CMV) infection results in destructive infections in neonates and immunocompromised individuals. Being the primary congenital infection in the United States, it can often… (more)

Subjects/Keywords: Benzimidazoles  – pharmacology<; br>; Cytomegalovirus<; br>; Enzyme Inhibitors  – pharmacology<; br>; Phosphotransferases (Alcohol Group Acceptor)  – chemistry<; br>; Phosphotransferases (Alcohol Group Acceptor)  – metabolism<; br>; Retinoblastoma Protein  – metabolism<; br>; Ribonucleosides  – pharmacology<; br>; Virus Replication

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APA (6th Edition):

Gill, R. B. (2011). Human cytomegalovirus UL97 kinase activity modifies cell cycle checkpoint regulators. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,867

Chicago Manual of Style (16th Edition):

Gill, Rachel B. “Human cytomegalovirus UL97 kinase activity modifies cell cycle checkpoint regulators.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed November 11, 2019. http://contentdm.mhsl.uab.edu/u?/etd,867.

MLA Handbook (7th Edition):

Gill, Rachel B. “Human cytomegalovirus UL97 kinase activity modifies cell cycle checkpoint regulators.” 2011. Web. 11 Nov 2019.

Vancouver:

Gill RB. Human cytomegalovirus UL97 kinase activity modifies cell cycle checkpoint regulators. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2019 Nov 11]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,867.

Council of Science Editors:

Gill RB. Human cytomegalovirus UL97 kinase activity modifies cell cycle checkpoint regulators. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,867

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