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Skip to Search Results- 1Campbell, Shelagh (Biological sciences)
- 1Dennis, Jonathan (Biological Sciences)
- 1Dr. Christine Szymanski (Department of Biological Sciences)
- 1Dr. Mario Feldman (Department of Biological Sciences)
- 1Dr. Tracy Raivio (Department of Biological Sciences)
- 1Murray, Alison (Biological Sciences)
Results for "Structural Engineering Reports"
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Spring 2016
maintaining pre-meiotic oocyte arrest in many animal models. Earlier reports from the Campbell lab, however, have shown that loss of Myt1 activity affected multiple aspects of Drosophila spermatogenesis resulting in male sterility. The conserved meiotic checkpoint function of Myt1 was hypothesized to account
overall coordination of G2/MI transition. Instead, the phenotypic analysis of myt1 mutants indicated that Myt1 activity is required for structural integrity of a germline specific membranous cytoskeletal organelle called the fusome (or intercellular bridges). I found that inhibition of Cyclin A-Cdk1
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Fall 2022
-sulfamethoxazole, whereas AXL3 is a novel virulent phage and candidate for genetic engineering. Additionally, I investigated the lack of in vivo data for S. maltophilia and show that type IV pili-binding phage DLP3 rescues Galleria mellonella larvae from lethal S. maltophilia infection. Further investigation into
the mechanism of host interactions for the type IV pili binding phages identified the surface exposed αβ-loop of the major pilin protein as a structural region important for phage binding, as well as two tail proteins in phage DLP2 as putative receptor binding proteins for cross-genera bacterial
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Mechanisms of Sensory Signal Transduction Across the Envelope in the CpxRA System of Escherichia coli
DownloadFall 2024
orientation may be present in other sensor kinases, revealing a previously unknown diversity in the structure of these common sensory domains. In Chapters 3 and 4, we investigate how the outer membrane lipoprotein NlpE activates CpxA in the presence of diverse inducing signals. We report the molecular details
of the interaction between NlpE and CpxA when NlpE is mislocalized to the inner membrane and examine the structural features of NlpE and their contribution to activating CpxA. We also find a role for the Cpx-regulated proteolytic factors CpxP and DegP in stabilizing NlpE, a novel axis of regulating
signaling from the outer membrane is coordinated through the cell wall. Finally, we report that NlpE can become surface-exposed, which may explain its ability to sense adhesion to surfaces. Thus, NlpE’s versatility in signaling comes from its ability to localize to both the inner and outer membranes, the
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Fall 2020
accompanied by morphological novelties, structural reductions and losses, hyperossifications, and increased intraspecific variation, which can create difficulties when establishing natural classifications. Traditionally, all “small” species of Alestidae with reduced multicuspid teeth were grouped in the tribe
size series for P. conserialis that addresses previous discrepancies in the literature regarding the presence or absence of a parietal fontanelle and reports the presence of a parietal fontanelle in all examined specimens. I document negative allometric growth between standard length and the length and
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Fall 2015
important to understand their generation, abundance and specific role(s). In addition, the mechanism of protein N-glycosylation and fOS generation by PglB are not well understood. This PhD thesis focuses on developing tools to study the generation, abundance and structural diversity of fOS. In addition, new
different between the two strains as determined by Western blot analysis with anti-N-glycan antibodies. This is the first report of the N-glycosylation of an OTase enzyme possibly affecting its own enzymatic activities. In order to better understand the N-glycosylation activity of PglB, a fluorescence
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Examination of IpLITR-mediated signal transduction events: the cross-talk regulation of phagocytosis
DownloadFall 2019
structural and phylogenetic relationships with vertebrate IgSF receptor-types. This family contains stimulatory and inhibitory forms that regulate several innate immune cell effector responses via classical as well as novel cytoplasmic tail (CYT)-dependent signaling capabilities. My thesis is focused on
demonstrated novel inhibitory signaling capabilities for IpLITR 1.1b, including the first report of cross-talk signaling potential within a teleost immunoregulatory receptor family. My work shows that teleost immunoregulatory receptors are excellent models to advance the understanding of innate