<HashMap><database>biostudies-other</database><scores/><additional><omics_type>Unknown</omics_type><volume>32</volume><submitter>Pauline Traynard</submitter><journal>Bioinformatics (Oxford, England)</journal><pagination>i772-i780</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/MODEL1611230001</full_dataset_link><repository>biostudies-other</repository><additional_accession>27587700</additional_accession><pubmed_authors>Pauline Traynard</pubmed_authors></additional><is_claimable>false</is_claimable><name>Traynard2016 - Mammalian cell cycle regulation - Logical Model</name><description>&lt;notes xmlns="http://www.sbml.org/sbml/level3/version1/core">      &lt;body xmlns="http://www.w3.org/1999/xhtml">        &lt;div class="dc:title">Traynard2016 - Mammalian cell cycleregulation - Logical Model&lt;/div>&lt;div class="dc:bibliographicCitation">  &lt;p>This model is described in the article:&lt;/p>  &lt;div class="bibo:title">    &lt;a href="http://identifiers.org/pubmed/27587700" title="Access to this publication">Logical model specification    aided by model-checking techniques: application to the    mammalian cell cycle regulation.&lt;/a>  &lt;/div>  &lt;div class="bibo:authorList">Traynard P, Fauré A, Fages F,  Thieffry D.&lt;/div>  &lt;div class="bibo:Journal">Bioinformatics 2016 Sep; 32(17):  i772-i780&lt;/div>  &lt;p>Abstract:&lt;/p>  &lt;div class="bibo:abstract">    &lt;p>Understanding the temporal behaviour of biological    regulatory networks requires the integration of molecular    information into a formal model. However, the analysis of model    dynamics faces a combinatorial explosion as the number of    regulatory components and interactions increases.We use    model-checking techniques to verify sophisticated dynamical    properties resulting from the model regulatory structure in the    absence of kinetic assumption. We demonstrate the power of this    approach by analysing a logical model of the molecular network    controlling mammalian cell cycle. This approach enables a    systematic analysis of model properties, the delineation of    model limitations, and the assessment of various refinements    and extensions based on recent experimental observations. The    resulting logical model accounts for the main irreversible    transitions between cell cycle phases, the sequential    activation of cyclins, and the inhibitory role of Skp2, and    further emphasizes the multifunctional role for the cell cycle    inhibitor Rb.The original and revised mammalian cell cycle    models are available in the model repository associated with    the public modelling software GINsim    (http://ginsim.org/node/189).thieffry@ens.frSupplementary data    are available at Bioinformatics online.&lt;/p>  &lt;/div>&lt;/div>&lt;div class="dc:publisher">  &lt;p>This model is hosted on   &lt;a href="http://www.ebi.ac.uk/biomodels/">BioModels Database&lt;/a>  and identified by:   &lt;a href="http://identifiers.org/biomodels.db/MODEL1611230001">MODEL1611230001&lt;/a>.&lt;/p>  &lt;p>To cite BioModels Database, please use:   &lt;a href="http://identifiers.org/pubmed/20587024" title="Latest BioModels Database publication">BioModels Database:  An enhanced, curated and annotated resource for published  quantitative kinetic models&lt;/a>.&lt;/p>&lt;/div>&lt;div class="dc:license">  &lt;p>To the extent possible under law, all copyright and related or  neighbouring rights to this encoded model have been dedicated to  the public domain worldwide. Please refer to   &lt;a href="http://creativecommons.org/publicdomain/zero/1.0/" title="Access to: CC0 1.0 Universal (CC0 1.0), Public Domain Dedication">CC0  Public Domain Dedication&lt;/a> for more information.&lt;/p>&lt;/div>&lt;/body>    &lt;/notes></description><dates><release>2016-11-23T00:00:00Z</release><modification>2025-07-14T17:55:35.469Z</modification><creation>2025-03-30T22:39:00.774Z</creation></dates><accession>MODEL1611230001</accession><cross_references><pubmed>27587700</pubmed><mamo>MAMO_0000030</mamo><unknown>null</unknown></cross_references></HashMap>