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You searched for +publisher:"University of Illinois – Urbana-Champaign" +contributor:("Blanke, Steven"). Showing records 1 – 17 of 17 total matches.

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University of Illinois – Urbana-Champaign

1. Jain, Prashant. Characterization of the Helicobacter pylori vacuolating cytotoxin mediated induction of mitochondrial cell death mechanism.

Degree: PhD, 0322, 2012, University of Illinois – Urbana-Champaign

 The Helicobacter pylori vacuolating cytotoxin (VacA) is a paradigm for microbial virulence factors that target and disable host cell mitochondria. VacA intoxication triggers mitochondrial dysfunction… (more)

Subjects/Keywords: Helicobacter pylori; Helicobacter pylori (VacA); Mitochondria; Cell death; Mitochondrial fission

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APA (6th Edition):

Jain, P. (2012). Characterization of the Helicobacter pylori vacuolating cytotoxin mediated induction of mitochondrial cell death mechanism. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/31964

Chicago Manual of Style (16th Edition):

Jain, Prashant. “Characterization of the Helicobacter pylori vacuolating cytotoxin mediated induction of mitochondrial cell death mechanism.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 20, 2019. http://hdl.handle.net/2142/31964.

MLA Handbook (7th Edition):

Jain, Prashant. “Characterization of the Helicobacter pylori vacuolating cytotoxin mediated induction of mitochondrial cell death mechanism.” 2012. Web. 20 Jul 2019.

Vancouver:

Jain P. Characterization of the Helicobacter pylori vacuolating cytotoxin mediated induction of mitochondrial cell death mechanism. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2142/31964.

Council of Science Editors:

Jain P. Characterization of the Helicobacter pylori vacuolating cytotoxin mediated induction of mitochondrial cell death mechanism. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/31964


University of Illinois – Urbana-Champaign

2. Gargi, Amandeep. Cellular interactions of the cytolethal distending toxins.

Degree: PhD, Microbiology, 2015, University of Illinois – Urbana-Champaign

 Over the course of evolution, pathogens have adapted and co-evolved with their respective hosts, with infectious diseases being one of the leading health concerns. Pathogens… (more)

Subjects/Keywords: Molecular Pathogenesis; Cellular Trafficking; Cytolethal Distending Toxin; Nuclear Microbiology

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APA (6th Edition):

Gargi, A. (2015). Cellular interactions of the cytolethal distending toxins. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/78769

Chicago Manual of Style (16th Edition):

Gargi, Amandeep. “Cellular interactions of the cytolethal distending toxins.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 20, 2019. http://hdl.handle.net/2142/78769.

MLA Handbook (7th Edition):

Gargi, Amandeep. “Cellular interactions of the cytolethal distending toxins.” 2015. Web. 20 Jul 2019.

Vancouver:

Gargi A. Cellular interactions of the cytolethal distending toxins. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2142/78769.

Council of Science Editors:

Gargi A. Cellular interactions of the cytolethal distending toxins. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/78769


University of Illinois – Urbana-Champaign

3. Gut, Ian M. The cellular and mechanistic study of nisin inhibition of bacillus anthracis spore outgrowth, nisin alteration of infection, and native producer immunity.

Degree: PhD, 0322, 2011, University of Illinois – Urbana-Champaign

 A critical step during Bacillus anthracis infection is the outgrowth of germinated spores into vegetative bacilli that proliferate and disseminate rapidly within the host. An… (more)

Subjects/Keywords: Nisin; germination; Bacillus anthracis; Lantibiotics; outgrowth

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APA (6th Edition):

Gut, I. M. (2011). The cellular and mechanistic study of nisin inhibition of bacillus anthracis spore outgrowth, nisin alteration of infection, and native producer immunity. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/24500

Chicago Manual of Style (16th Edition):

Gut, Ian M. “The cellular and mechanistic study of nisin inhibition of bacillus anthracis spore outgrowth, nisin alteration of infection, and native producer immunity.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 20, 2019. http://hdl.handle.net/2142/24500.

MLA Handbook (7th Edition):

Gut, Ian M. “The cellular and mechanistic study of nisin inhibition of bacillus anthracis spore outgrowth, nisin alteration of infection, and native producer immunity.” 2011. Web. 20 Jul 2019.

Vancouver:

Gut IM. The cellular and mechanistic study of nisin inhibition of bacillus anthracis spore outgrowth, nisin alteration of infection, and native producer immunity. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2142/24500.

Council of Science Editors:

Gut IM. The cellular and mechanistic study of nisin inhibition of bacillus anthracis spore outgrowth, nisin alteration of infection, and native producer immunity. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/24500


University of Illinois – Urbana-Champaign

4. Kotil, Seyfullah Enes. Requirements and strategies for winning the battle against antibiotic resistance by antisense technology.

Degree: PhD, Biophysics & Computnl Biology, 2016, University of Illinois – Urbana-Champaign

 In chapter 1 we have investigated the different requirements and conditions for efficiency and specificity of antisense molecules. For specific therapy, an antibacterial RNA must… (more)

Subjects/Keywords: Antibiotic resistance; Evolution of antibiotic resistance; designing antisense molecules; off-target; sustainable therapy; reversing antibiotic resistance; blocking antibiotic resistance; guiding antibiotic resistance; directed evolution

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APA (6th Edition):

Kotil, S. E. (2016). Requirements and strategies for winning the battle against antibiotic resistance by antisense technology. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95600

Chicago Manual of Style (16th Edition):

Kotil, Seyfullah Enes. “Requirements and strategies for winning the battle against antibiotic resistance by antisense technology.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 20, 2019. http://hdl.handle.net/2142/95600.

MLA Handbook (7th Edition):

Kotil, Seyfullah Enes. “Requirements and strategies for winning the battle against antibiotic resistance by antisense technology.” 2016. Web. 20 Jul 2019.

Vancouver:

Kotil SE. Requirements and strategies for winning the battle against antibiotic resistance by antisense technology. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2142/95600.

Council of Science Editors:

Kotil SE. Requirements and strategies for winning the battle against antibiotic resistance by antisense technology. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95600


University of Illinois – Urbana-Champaign

5. Molohon Hess, Katie Jo. Structure and function analysis of the natural product plantazolicin, a bacillus anthracis-specific antibiotic.

Degree: PhD, Microbiology, 2015, University of Illinois – Urbana-Champaign

 Bacteria are a fruitful source of metabolites, many of which have been the scaffolds for the majority of approved antibiotic compounds. In this dissertation, I… (more)

Subjects/Keywords: Plantazolicin; Natural product; Bacillus anthracis; Mode of action

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APA (6th Edition):

Molohon Hess, K. J. (2015). Structure and function analysis of the natural product plantazolicin, a bacillus anthracis-specific antibiotic. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89125

Chicago Manual of Style (16th Edition):

Molohon Hess, Katie Jo. “Structure and function analysis of the natural product plantazolicin, a bacillus anthracis-specific antibiotic.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 20, 2019. http://hdl.handle.net/2142/89125.

MLA Handbook (7th Edition):

Molohon Hess, Katie Jo. “Structure and function analysis of the natural product plantazolicin, a bacillus anthracis-specific antibiotic.” 2015. Web. 20 Jul 2019.

Vancouver:

Molohon Hess KJ. Structure and function analysis of the natural product plantazolicin, a bacillus anthracis-specific antibiotic. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2142/89125.

Council of Science Editors:

Molohon Hess KJ. Structure and function analysis of the natural product plantazolicin, a bacillus anthracis-specific antibiotic. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89125


University of Illinois – Urbana-Champaign

6. Walling, Brent. The effect of helical carbon nanotubes on macrophage function.

Degree: PhD, 0361, 2014, University of Illinois – Urbana-Champaign

 Occupational and environmental pulmonary exposure to carbon nanotubes (CNT) is considered to be a health risk with a very low threshold of tolerance as determined… (more)

Subjects/Keywords: Helical carbon nanotubes; lung; inflammation; macrophages; phagocytosis; Pseudomonas aeruginosa

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APA (6th Edition):

Walling, B. (2014). The effect of helical carbon nanotubes on macrophage function. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/46915

Chicago Manual of Style (16th Edition):

Walling, Brent. “The effect of helical carbon nanotubes on macrophage function.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 20, 2019. http://hdl.handle.net/2142/46915.

MLA Handbook (7th Edition):

Walling, Brent. “The effect of helical carbon nanotubes on macrophage function.” 2014. Web. 20 Jul 2019.

Vancouver:

Walling B. The effect of helical carbon nanotubes on macrophage function. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2142/46915.

Council of Science Editors:

Walling B. The effect of helical carbon nanotubes on macrophage function. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/46915


University of Illinois – Urbana-Champaign

7. Tsang, Ying-Hung N. Regulation of RUNX3 in gastric and breast cancer.

Degree: PhD, 0318, 2012, University of Illinois – Urbana-Champaign

 RUNX3 is a transcription factor that is ubiquitously expressed in different tissues and has been shown to have diverse functions in many developmental procedures. Recently… (more)

Subjects/Keywords: Runt-related transcription factor 3 (RUNX3); cytotoxin-associated gene A (CagA); Pin1; Gastric cancer; Breast cancer

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APA (6th Edition):

Tsang, Y. N. (2012). Regulation of RUNX3 in gastric and breast cancer. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/29531

Chicago Manual of Style (16th Edition):

Tsang, Ying-Hung N. “Regulation of RUNX3 in gastric and breast cancer.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 20, 2019. http://hdl.handle.net/2142/29531.

MLA Handbook (7th Edition):

Tsang, Ying-Hung N. “Regulation of RUNX3 in gastric and breast cancer.” 2012. Web. 20 Jul 2019.

Vancouver:

Tsang YN. Regulation of RUNX3 in gastric and breast cancer. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2142/29531.

Council of Science Editors:

Tsang YN. Regulation of RUNX3 in gastric and breast cancer. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/29531


University of Illinois – Urbana-Champaign

8. Jiang, Song. Defining the role of toll-like receptor 10 in immune signaling.

Degree: PhD, Microbiology, 2016, University of Illinois – Urbana-Champaign

 Toll-like Receptors (TLRs) represent a class of pattern recognition receptors that function to recognize invading microbes and initiate pro-inflammatory responses. TLR10 is the only remaining… (more)

Subjects/Keywords: Toll-like Receptor 10; TLR; Immune signaling

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APA (6th Edition):

Jiang, S. (2016). Defining the role of toll-like receptor 10 in immune signaling. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/92894

Chicago Manual of Style (16th Edition):

Jiang, Song. “Defining the role of toll-like receptor 10 in immune signaling.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 20, 2019. http://hdl.handle.net/2142/92894.

MLA Handbook (7th Edition):

Jiang, Song. “Defining the role of toll-like receptor 10 in immune signaling.” 2016. Web. 20 Jul 2019.

Vancouver:

Jiang S. Defining the role of toll-like receptor 10 in immune signaling. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2142/92894.

Council of Science Editors:

Jiang S. Defining the role of toll-like receptor 10 in immune signaling. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/92894


University of Illinois – Urbana-Champaign

9. Clemons, Nathan Cortelius. Escape to the interior: Characterization of the cytosolic delivery of C-terminal cargo subdomains by the N-terminus of pasteurella multocida toxin and subsequent toxin-mediated downregulation of Gaq-PLCb1 signaling through depletion of Gaq from the plasma membrane.

Degree: PhD, Microbiology, 2018, University of Illinois – Urbana-Champaign

 The bacterium Pasteurella multocida is a gram-negative, non-spore- forming, capsulated coccobacillus that lives an aerobic to facultative anaerobic lifestyle. P. multocida is a zoonotic pathogen… (more)

Subjects/Keywords: Pasteurella multocida Modular Protein Toxin

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APA (6th Edition):

Clemons, N. C. (2018). Escape to the interior: Characterization of the cytosolic delivery of C-terminal cargo subdomains by the N-terminus of pasteurella multocida toxin and subsequent toxin-mediated downregulation of Gaq-PLCb1 signaling through depletion of Gaq from the plasma membrane. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/102384

Chicago Manual of Style (16th Edition):

Clemons, Nathan Cortelius. “Escape to the interior: Characterization of the cytosolic delivery of C-terminal cargo subdomains by the N-terminus of pasteurella multocida toxin and subsequent toxin-mediated downregulation of Gaq-PLCb1 signaling through depletion of Gaq from the plasma membrane.” 2018. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 20, 2019. http://hdl.handle.net/2142/102384.

MLA Handbook (7th Edition):

Clemons, Nathan Cortelius. “Escape to the interior: Characterization of the cytosolic delivery of C-terminal cargo subdomains by the N-terminus of pasteurella multocida toxin and subsequent toxin-mediated downregulation of Gaq-PLCb1 signaling through depletion of Gaq from the plasma membrane.” 2018. Web. 20 Jul 2019.

Vancouver:

Clemons NC. Escape to the interior: Characterization of the cytosolic delivery of C-terminal cargo subdomains by the N-terminus of pasteurella multocida toxin and subsequent toxin-mediated downregulation of Gaq-PLCb1 signaling through depletion of Gaq from the plasma membrane. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2018. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2142/102384.

Council of Science Editors:

Clemons NC. Escape to the interior: Characterization of the cytosolic delivery of C-terminal cargo subdomains by the N-terminus of pasteurella multocida toxin and subsequent toxin-mediated downregulation of Gaq-PLCb1 signaling through depletion of Gaq from the plasma membrane. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2018. Available from: http://hdl.handle.net/2142/102384

10. Maxson, Tucker. Stimulating antibiotic development by targeting virulence and facilitating natural product discovery.

Degree: PhD, Chemistry, 2016, University of Illinois – Urbana-Champaign

 Antibiotics are a cornerstone of modern medicine and have drastically reduced the burden of infectious diseases. Unfortunately, resistance to all clinically used antibiotics has become… (more)

Subjects/Keywords: virulence; nelfinavir; CaaX protease; natural products; reactivity based screening

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APA (6th Edition):

Maxson, T. (2016). Stimulating antibiotic development by targeting virulence and facilitating natural product discovery. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/90486

Chicago Manual of Style (16th Edition):

Maxson, Tucker. “Stimulating antibiotic development by targeting virulence and facilitating natural product discovery.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 20, 2019. http://hdl.handle.net/2142/90486.

MLA Handbook (7th Edition):

Maxson, Tucker. “Stimulating antibiotic development by targeting virulence and facilitating natural product discovery.” 2016. Web. 20 Jul 2019.

Vancouver:

Maxson T. Stimulating antibiotic development by targeting virulence and facilitating natural product discovery. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2142/90486.

Council of Science Editors:

Maxson T. Stimulating antibiotic development by targeting virulence and facilitating natural product discovery. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/90486


University of Illinois – Urbana-Champaign

11. Brothers, Michael. Toxin-membrane interactions of Pasteurella multocida toxin and homologous domains.

Degree: PhD, 0335, 2014, University of Illinois – Urbana-Champaign

 Toxin-membrane interactions are poorly understood on the molecular level due to the inherent difficulty of crystallizing membrane protein complexes and the large size (>50 kDa)… (more)

Subjects/Keywords: Nuclear magnetic resonance (NMR) spectroscopy; Pasteurella multocida toxin; Membrane Localization Domain; Four Helix Bundle

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APA (6th Edition):

Brothers, M. (2014). Toxin-membrane interactions of Pasteurella multocida toxin and homologous domains. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/49777

Chicago Manual of Style (16th Edition):

Brothers, Michael. “Toxin-membrane interactions of Pasteurella multocida toxin and homologous domains.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 20, 2019. http://hdl.handle.net/2142/49777.

MLA Handbook (7th Edition):

Brothers, Michael. “Toxin-membrane interactions of Pasteurella multocida toxin and homologous domains.” 2014. Web. 20 Jul 2019.

Vancouver:

Brothers M. Toxin-membrane interactions of Pasteurella multocida toxin and homologous domains. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2142/49777.

Council of Science Editors:

Brothers M. Toxin-membrane interactions of Pasteurella multocida toxin and homologous domains. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/49777


University of Illinois – Urbana-Champaign

12. Kim, Seyeun. Structure-function analysis of IntDOT, the CTnDOT integrase.

Degree: PhD, 0322, 2011, University of Illinois – Urbana-Champaign

 IntDOT is an enzyme required for the recombination reactions that promote movement of CTnDOT that is an integrative conjugative element (ICE) found in Bacteroides spp.… (more)

Subjects/Keywords: Tyrosine recombinase family; Bacteroides conjugative transposon (CTnDOT); CTnDOT integrase (IntDOT)

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APA (6th Edition):

Kim, S. (2011). Structure-function analysis of IntDOT, the CTnDOT integrase. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/18325

Chicago Manual of Style (16th Edition):

Kim, Seyeun. “Structure-function analysis of IntDOT, the CTnDOT integrase.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 20, 2019. http://hdl.handle.net/2142/18325.

MLA Handbook (7th Edition):

Kim, Seyeun. “Structure-function analysis of IntDOT, the CTnDOT integrase.” 2011. Web. 20 Jul 2019.

Vancouver:

Kim S. Structure-function analysis of IntDOT, the CTnDOT integrase. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2142/18325.

Council of Science Editors:

Kim S. Structure-function analysis of IntDOT, the CTnDOT integrase. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/18325


University of Illinois – Urbana-Champaign

13. Randall, Crystal. Characterization of the anti-inflammatory effects of the Molluscum Contagiosum MC159 protein.

Degree: PhD, 0322, 2013, University of Illinois – Urbana-Champaign

 The Molluscum Contagiosum Virus (MCV) is a dermotropic poxvirus that strictly infects humans. MCV infections produce umbilicated lesions that can persist for six to nine… (more)

Subjects/Keywords: Poxviruses; Immune evasion

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APA (6th Edition):

Randall, C. (2013). Characterization of the anti-inflammatory effects of the Molluscum Contagiosum MC159 protein. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/44818

Chicago Manual of Style (16th Edition):

Randall, Crystal. “Characterization of the anti-inflammatory effects of the Molluscum Contagiosum MC159 protein.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 20, 2019. http://hdl.handle.net/2142/44818.

MLA Handbook (7th Edition):

Randall, Crystal. “Characterization of the anti-inflammatory effects of the Molluscum Contagiosum MC159 protein.” 2013. Web. 20 Jul 2019.

Vancouver:

Randall C. Characterization of the anti-inflammatory effects of the Molluscum Contagiosum MC159 protein. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2142/44818.

Council of Science Editors:

Randall C. Characterization of the anti-inflammatory effects of the Molluscum Contagiosum MC159 protein. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/44818


University of Illinois – Urbana-Champaign

14. Willis, Kristen L. Characterization of the anti-viral effects inhibited by the vaccinia virus K1 protein.

Degree: PhD, 0322, 2011, University of Illinois – Urbana-Champaign

 Vaccinia virus (VV), a member of the poxvirus family of double-stranded DNA viruses, is well-known as a highly effective vaccine against variola virus, the causative… (more)

Subjects/Keywords: vaccinia virus; protein kinase (PKR); NF-kappaB; K1 protein

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APA (6th Edition):

Willis, K. L. (2011). Characterization of the anti-viral effects inhibited by the vaccinia virus K1 protein. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/18499

Chicago Manual of Style (16th Edition):

Willis, Kristen L. “Characterization of the anti-viral effects inhibited by the vaccinia virus K1 protein.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 20, 2019. http://hdl.handle.net/2142/18499.

MLA Handbook (7th Edition):

Willis, Kristen L. “Characterization of the anti-viral effects inhibited by the vaccinia virus K1 protein.” 2011. Web. 20 Jul 2019.

Vancouver:

Willis KL. Characterization of the anti-viral effects inhibited by the vaccinia virus K1 protein. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2142/18499.

Council of Science Editors:

Willis KL. Characterization of the anti-viral effects inhibited by the vaccinia virus K1 protein. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/18499

15. Smith, Lucas. Molecular characterization of a sphingomyelin binding site in the vacuolating cytotoxin of H. pylori.

Degree: MS, 0314, 2014, University of Illinois – Urbana-Champaign

 The main determinants in toxin cell specificity are often interactions with surface receptors. It has recently been determined that the membrane phospholipid sphingomyelin (SM) is… (more)

Subjects/Keywords: Stomach Cancer; Gastric Adenocarcinoma; H.pylori; Helicobacter pylori; Vacuolating Cytotoxin (VacA); Toxin; Sphingomyelin

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APA (6th Edition):

Smith, L. (2014). Molecular characterization of a sphingomyelin binding site in the vacuolating cytotoxin of H. pylori. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/49596

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):

Smith, Lucas. “Molecular characterization of a sphingomyelin binding site in the vacuolating cytotoxin of H. pylori.” 2014. Thesis, University of Illinois – Urbana-Champaign. Accessed July 20, 2019. http://hdl.handle.net/2142/49596.

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

MLA Handbook (7th Edition):

Smith, Lucas. “Molecular characterization of a sphingomyelin binding site in the vacuolating cytotoxin of H. pylori.” 2014. Web. 20 Jul 2019.

Vancouver:

Smith L. Molecular characterization of a sphingomyelin binding site in the vacuolating cytotoxin of H. pylori. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2142/49596.

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

Council of Science Editors:

Smith L. Molecular characterization of a sphingomyelin binding site in the vacuolating cytotoxin of H. pylori. [Thesis]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/49596

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

16. Wetzel, Margaret Elizabeth. Characterization of an agrobacterial plasmid inducible for transfer by mannopine and evolution of the core replication and transfer functions of repabc plasmids with class i quorum-sensing and transfer systems.

Degree: PhD, Microbiology, 2016, University of Illinois – Urbana-Champaign

 repABC plasmids are ubiquitous in the α-proteobacteria and are important to the biology of the bacteria that harbor them for several reasons. First, they can… (more)

Subjects/Keywords: quorum-sensing; conjugative transfer; opines; mannopine; Alphaproteobacteria; RepABC; conjugative transfer genes; horizontal transfer; plasmid evolution

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

APA (6th Edition):

Wetzel, M. E. (2016). Characterization of an agrobacterial plasmid inducible for transfer by mannopine and evolution of the core replication and transfer functions of repabc plasmids with class i quorum-sensing and transfer systems. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95287

Chicago Manual of Style (16th Edition):

Wetzel, Margaret Elizabeth. “Characterization of an agrobacterial plasmid inducible for transfer by mannopine and evolution of the core replication and transfer functions of repabc plasmids with class i quorum-sensing and transfer systems.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 20, 2019. http://hdl.handle.net/2142/95287.

MLA Handbook (7th Edition):

Wetzel, Margaret Elizabeth. “Characterization of an agrobacterial plasmid inducible for transfer by mannopine and evolution of the core replication and transfer functions of repabc plasmids with class i quorum-sensing and transfer systems.” 2016. Web. 20 Jul 2019.

Vancouver:

Wetzel ME. Characterization of an agrobacterial plasmid inducible for transfer by mannopine and evolution of the core replication and transfer functions of repabc plasmids with class i quorum-sensing and transfer systems. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2142/95287.

Council of Science Editors:

Wetzel ME. Characterization of an agrobacterial plasmid inducible for transfer by mannopine and evolution of the core replication and transfer functions of repabc plasmids with class i quorum-sensing and transfer systems. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95287

17. Park, Ji-Yeon. Positive regulators of Bacteroides CTnDOT excision and transfer.

Degree: PhD, 0322, 2012, University of Illinois – Urbana-Champaign

 Tetracycline stimulates both excision and transfer of a Bacteroides Conjugative transposon CTnDOT. It was shown previously that a gene, rteC, is necessary for tetracycline-stimulated transcriptional… (more)

Subjects/Keywords: Bacteroides; CTnDOT; Gene regulation

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

APA (6th Edition):

Park, J. (2012). Positive regulators of Bacteroides CTnDOT excision and transfer. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/29526

Chicago Manual of Style (16th Edition):

Park, Ji-Yeon. “Positive regulators of Bacteroides CTnDOT excision and transfer.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 20, 2019. http://hdl.handle.net/2142/29526.

MLA Handbook (7th Edition):

Park, Ji-Yeon. “Positive regulators of Bacteroides CTnDOT excision and transfer.” 2012. Web. 20 Jul 2019.

Vancouver:

Park J. Positive regulators of Bacteroides CTnDOT excision and transfer. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Jul 20]. Available from: http://hdl.handle.net/2142/29526.

Council of Science Editors:

Park J. Positive regulators of Bacteroides CTnDOT excision and transfer. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/29526

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