Team:ULB-Brussels/Modelling

From 2014.igem.org

(Difference between revisions)
m
Line 23: Line 23:
</td></tr>
</td></tr>
</table>
</table>
-
</br>
+
<br/>
-
<table style="background-color:rgb(204,214,234);" width="90%"  align="center">
+
<table style="background-color:#ebebeb;" width="90%"  align="center">
-
<tr style="background-color:rgb(246,246,246);">
+
<tr style="background-color:rgb(245,245,245);">
-
<!--<td>
+
<td colspan="2">
-
<br/>-->
+
<br/>
<section style="margin: -40px"></section>
<section style="margin: -40px"></section>
<section style="text-align: justify; margin: 50px">
<section style="text-align: justify; margin: 50px">
-
<!-- Nice Biblio effect with: </table>  
+
<</td>
-
<table style="background-color:rgb(204,214,234)"> -->
+
-
 
+
-
</section>
+
-
<section style="background-color:#CCD6EA; margin: 25px">
+
-
<section style="text-align: justify; margin: 25px">
+
-
<h3>$\hspace{0.12cm}$Bibliography</h3>
+
-
<!-- Rem: Biblio written by chronology, from 1910 until 2014 -->
+
-
<ul>
+
-
<li>[13]  A.V. Hill, (1910). <i>The possible effects of the Aggregation of the molecules of hemoglobin on its Dissociation curves</i>, J. Physiol, No.40, iv-vii. </li>
+
-
<!-- Intro on Hill functions with hemoglobin-->
+
-
<li>[14] T. Ogura, S. Hiraga, (1983). <i>Mini-F plasmids genes that couple Host cell division to Plasmid proliferation</i>, Proc. Natl. Acad. Sci. USA, 80, 4784-4788. </li>
+
-
<!--
+
-
(Abstract): Stable Maintenance plasmids, ccd region dissected into ccdB (cell division) and ccdA (inhibition), plasmid proloferation.
+
-
(p4785): oriC plasmids, EcoR1, replication
+
-
(p4787): Dissection of the cdd region + culture, kinetics and growing conditions.
+
-
(p4788): Mutants of F plasmid
+
-
-->
+
-
<li>[15]  M. Santillán, (2008). <i>On the use of the Hill functions in Mathematical models od Gene regulatory networks</i>, Math. Model. Nat. Phenom., Vol.3, No.2, 85-97. </li>
+
-
<!--
+
-
(p86): Cooperative binding sequences: The Hill coefficient is appropriately described as an interaction coefficient reflecting cooperativity.
+
-
(p94): If P is an activator(/repressor), the regulatory function R([P]) comes out to be monotocally increasing(/decreasing). Transcription rate, probability of gene copy.
+
-
(p95): Interestingly, the most extensively studied gene regulatory systems (cf lactose operon of E.coli) make use of cooperativity to increase the sigmoidicity of the regulatory functions.
+
-
(p96): Significance of the parameters by modelling.
+
-
-->
+
-
<li>[16] P. Wang, R.E. Dalbey, (2010). <i>In Vitro and in Vivo approaches to studying the Bacterial signal Peptide processing</i>, Springer Protocols, A. Economou ed. Humana Press, Protein Secretion, Methods in Molecular Biology 619,  21-37. </li>
+
-
<!-- Signal peptide cleavage, membranes, cell biology, in vitro assays. -->
+
-
<li>[17]  L. Gelens, L. Hill, A. Vandervelde, J. Danckaert, R. Loris, (2013). <i>A general model for Toxin-antitoxin module dynamics can explain Persister cell formation in E.coli</i>, PLOS Computational Biology, Vol.9, Iss.8, e1003190. </li>
+
-
<!--
+
-
(p1): Among the elements involved in bacterial stress response are the type TT toxine-antitoxin modules. CcdB and ParE family mambers inhibit gyrase, although via different molecular mechanisms.
+
-
(p2): Persisters are subpopulations of bacteria wich are tolerant to biological stresses such antibiotics because they are in a dormant, non-dividing state.
+
-
(p11): Fig @ simulations: Large toxin spikes -> route to persister cell formation through growth rate suppression.
+
-
(p14): Kinds of TA, TAT Decay complexes.
+
-
-->
+
-
<li>[18] N. Goeders, L. Van Melderen, (2014). <i>Toxin-antitoxin systems as Multilevel interaction systems</i>, Toxins, 6, 304-324, ISSN 2072-6651. </li>
+
-
<!--
+
-
(p305): Fig: ccdA-ccdB
+
-
(p306): Evolution of TA systems + bioinfo approaches.
+
-
(p313): Effect on DNA-gyrase.
+
-
-->
+
-
<li>[19] D.A. Malyshev, K. Dhami, T. Lavergne, T. Chen, N. Dai, J.M. Foster, I.R. Corrêa Jr & F.E. Romesberg, (2014).
+
-
<i>A semi-synthetic organism with an expanded genetic alphabet</i>, Research Letter, Nature 13314, 1-17. </li>
+
-
<!-- E.Coli, experimental results using IPTG and KPI, iGEM 2013 team -->
+
-
<li>[20] A. Provata, C. Nicolis & G. Nicolis, (2014). <i>DNA viewed as an out-of-equilibrium structure</i>, Phys. Rev. E 89, 052105. </li>
+
-
<!-- Stochasticity and Markov processes, mammal chromosomes, MC rejection method algorithm, short-ranged intermolecular interactions. -->
+
-
</ul>
+
-
<br>
+
-
</section></section>
+
-
 
+
-
<section style="margin: -5px"></section>
+
-
</tr>
+
-
 
+
-
 
+
<!-- Previous and Next pages -->
<!-- Previous and Next pages -->
<tr style="background-color:rgb(204,214,234);"><td>
<tr style="background-color:rgb(204,214,234);"><td>
Line 90: Line 38:
<section style="text-align: right">
<section style="text-align: right">
<a href="https://2014.igem.org/Team:ULB-Brussels/Modelling/Population-Dynamics"><b> Population Dynamics > </b></a>
<a href="https://2014.igem.org/Team:ULB-Brussels/Modelling/Population-Dynamics"><b> Population Dynamics > </b></a>
-
</section>
+
</section></tr>
-
</tr>
+
<tr><td><br/><br/></td></tr>
<tr><td><br/><br/></td></tr>
-
</table></th></tr>
+
</th></tr>
</div>
</div>

Revision as of 22:46, 17 October 2014

$~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ \newcommand{\MyColi}{{\small Mighty\hspace{0.12cm}Coli}} \newcommand{\Stabi}{\small Stabi}$ $\newcommand{\EColi}{\small E.coli} \newcommand{\SCere}{\small S.cerevisae}\\[0cm] ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ \newcommand{\PI}{\small PI}$ $\newcommand{\Igo}{\Large\mathcal{I}} \newcommand{\Tgo}{\Large\mathcal{T}} \newcommand{\Ogo}{\Large\mathcal{O}} ~$ Example of a hierarchical menu in CSS

carousel slider




- Université Libre de Bruxelles -


'Now begins an $Overview$ about Modelling'


Retrieved from "http://2014.igem.org/Team:ULB-Brussels/Modelling"

<
Population Dynamics >