1,725,626 research outputs found
WSC Alum
Get PDFThe WSC Alum was a publication of Winona State College. It is published for alumni and friends of the College in an effort to keep them aware of progress and news on the campus and to help them maintain contact with one another. - WSC Alum Spring 1970https://openriver.winona.edu/wscalum/1000/thumbnail.jp
Characteristics of the Δ<i>wsc-1</i> and Δ<i>wsc-2</i> mutants.
No full text<p>(<b>A</b>) The organization of the WSC-1 and WSC-2 proteins includes a N terminal extracellular region with a WSC domain (and a serine/threonine-rich region in WSC-2), a transmembrane helical sequence (TMH), and an intracellular carboxyl terminus. (<b>B</b>) Growth rates for wild type, Δ<i>wsc-1</i>, Δ<i>wsc-2</i>, Δ<i>wsc-1;</i> Δ<i>wsc-2</i>, and Δ<i>mak-1</i> are shown. (<b>C</b>) Images of the colony morphology (upper panel), the production of protoperithecia on Cornmeal agar (middle panel), and CAT fusion (lower panel) for wild type, Δ<i>wsc-1</i>, Δ<i>wsc-2</i>, Δ<i>wsc-1;</i> Δ<i>wsc-2</i>, and Δ<i>mak-1</i> are shown. The arrows in the middle and lower panels point to protoperithecia and CAT fusions.</p
Simulation and verification for computational modelling of signalling pathways
No full textModelling of the dynamics of biochemical reaction networks typically proceeds by solving ordinary differential equations or stochastic simulation via the Gillespie algorithm. More recently, computational methods such as process algebra techniques have been successfully applied to the analysis of signalling pathways. One advantage of these is that they enable automatic verification of the models, via model checking, against qualitative and quantitative temporal logic specifications, for example, "what is the probability that the protein eventually degrades?". Such verification is exhaustive, that is, the analysis is carried out over all paths, producing exact quantitative measures. In this paper, we give an overview of the simulation, verification and differential equation approaches to modelling biochemical reaction networks. We discuss the advantages and disadvantages of the respective methods, using as an illustration a fragment of the FGF signalling pathway. © 2006 IEEE
Pyramiding of favorable WSC alleles enhanced WSC and TGW under various water conditions.
No full text<p><sup>1</sup> Values with different letters in columns are significantly different (P <0.05).</p><p>Pyramiding of favorable WSC alleles enhanced WSC and TGW under various water conditions.</p
Building Parallel Time-Constrained HLA Federates: A Case Study with the PARSEC Parallel Simulation Language
No full textInternational audienceBased on the DIS result, the HLA framework has been defined to achieve interoperability of independent simulators. Concurrently, and for the most part, independent of that effort, the parallel and distributed simulation community has attempted to define synchronization protocols for the correct execution of parallel simulation as-fast-as possible. Building parallel time-constrained federates within an HLA framework is not an easy task. We identify the potential difficulties: one or several federates, when and how to advance the federate's time, how to handle RTI notifications, etc., and present our experiences with adding HLA features into the PARSEC parallel simulation language
UMC/ WSC Baseball Games Changed
No full textVito, Chris. (2008). UMC/ WSC Baseball Games Changed. Retrieved from the University Digital Conservancy, https://hdl.handle.net/11299/221535
Complementation and RIP analysis of <i>wsc-1</i>.
No full text<p>Colony morphologies are shown for wild type, Δ<i>wsc-1</i>, a transformant of Δ<i>wsc-1</i> containing a wild type copy of the <i>wsc-1</i> gene inserted at the <i>his-3</i> locus, and the <i>wsc-1<sup>RIP1</sup></i> mutant grown for 24 hours on a Vogel’s sucrose agar medium.</p
Δ<i>wsc-1</i>, Δ<i>ham-7</i>, and Δ<i>wsc-1;</i>
No full text<p><b>Δ</b><b><i>ham-7</i></b><b> are deficient in MAK-1 activation.</b> (<b>A</b>) In the upper panel, extracts of non-stressed and oxidatively stressed wild type, Δ<i>wsc-1</i>, Δ<i>ham-7</i>, and Δ<i>wsc-1;</i> Δ<i>ham-7</i> cells were prepared and assayed for the presence of phosphorylated MAK-1 and MAK-2 by a Western blot assay using antibody that specifically recognizes the phosphorylated proteins. Extracts from non-stressed and from stressed cells are denoted by – and +. The sizes of the MAK-1 and MAK-2 proteins are shown at the side of the Western blot. A Western blot against tubulin was used as a control and to calibrate the amounts of protein in each of the samples. The amounts of activated MAK-1 (middle panel) and MAK-2 (lower panel) in each of the samples relative to the amount of activated MAK-1 or MAK-2 in the non-stressed wild type cell are shown (n = 5). (<b>B</b>) The colony extension rates for wild type, Δ<i>wsc-1</i>, Δ<i>ham-7</i>, Δ<i>wsc-1;</i> Δ<i>ham-7</i>, and Δ<i>mak-1</i> are shown. (<b>C</b>) The colony morphology (upper panel), the lack of protoperithecia production (middle panel), and lack of CAT fusion (lower panel) are shown for Δ<i>wsc-1;</i> Δ<i>ham-7</i>, and Δ<i>mak-1</i>.</p
Fermentation performance of Y128 under varying concentrations of WSC.
No full text(A) Glucose consumption; (B), Xylose consumption; (C), Ethanol production and (D), Cell growth OD600. Syn-4WSC: SynH with 40 g/L WSC added; SynH-3WSC: SynH with 30 g/L WSC added; SynH 2WSC: SynH with 20 g/L WSC added; SynH-1WSC: SynH with 10 g/L WSC added; SynH-Control: SynH-base media with no inhibitors added. Fermentation was conducted in Erlenmeyer flasks (50 mL) at pH 4.8, 30 °C and 150 RPM with inoculum at 2 (OD600).</p
Workplace social capital (WSC) dimensions and indicators.
No full text<p>Workplace social capital (WSC) dimensions and indicators.</p
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