<?xml version="1.0" encoding="utf-8"?>
<export-example>
  <doc>
    <id>2730</id>
    <completedYear/>
    <publishedYear>2018</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst/>
    <pageLast/>
    <pageNumber>15</pageNumber>
    <edition/>
    <issue>4</issue>
    <volume>8 (2018)</volume>
    <articleNumber>158</articleNumber>
    <type>article</type>
    <publisherName>MDPI</publisherName>
    <publisherPlace>Basel</publisherPlace>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>0</belongsToBibliography>
    <completedDate>2022-08-23</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">Semantic Multi-Classifier Systems Identify Predictive Processes in Heart Failure Models across Species</title>
    <abstract language="eng">Genetic model organisms have the potential of removing blind spots from the underlying gene regulatory networks of human diseases. Allowing analyses under experimental conditions they complement the insights gained from observational data. An inevitable requirement for a successful trans-species transfer is an abstract but precise high-level characterization of experimental findings. In this work, we provide a large-scale analysis of seven weak contractility/heart failure genotypes of the model organism zebrafish which all share a weak contractility phenotype. In supervised classification experiments, we screen for discriminative patterns that distinguish between observable phenotypes (homozygous mutant individuals) as well as wild-type (homozygous wild-types) and carriers (heterozygous individuals). As the method of choice we use semantic multi-classifier systems, a knowledge-based approach which constructs hypotheses from a predefined vocabulary of high-level terms (e.g., Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways or Gene Ontology (GO) terms). Evaluating these models leads to a compact description of the underlying processes and guides the screening for new molecular markers of heart failure. Furthermore, we were able to independently corroborate the identified processes in Wistar rats.</abstract>
    <parentTitle language="eng">Biomolecules</parentTitle>
    <identifier type="issn">2218-273X</identifier>
    <identifier type="urn">urn:nbn:de:bvb:573-27303</identifier>
    <note>This article belongs to the Special Issue "Biomolecules for Translational Approaches in Cardiology"</note>
    <enrichment key="THI_relatedIdentifier">https://doi.org/10.3390/biom8040158</enrichment>
    <enrichment key="THI_articleversion">published</enrichment>
    <enrichment key="THI_review">peer-review</enrichment>
    <enrichment key="THI_openaccess">ja</enrichment>
    <enrichment key="opus.source">publish</enrichment>
    <licence>Creative Commons BY 4.0</licence>
    <author>
      <first_name>Ludwig</first_name>
      <last_name>Lausser</last_name>
    </author>
    <author>
      <first_name>Lea</first_name>
      <last_name>Kubis</last_name>
    </author>
    <author>
      <first_name>Wolfgang</first_name>
      <last_name>Rottbauer</last_name>
    </author>
    <author>
      <first_name>Derk</first_name>
      <last_name>Frank</last_name>
    </author>
    <author>
      <first_name>Steffen</first_name>
      <last_name>Just</last_name>
    </author>
    <author>
      <first_name>Hans A.</first_name>
      <last_name>Kestler</last_name>
    </author>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>heart failure phenotypes</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>zebrafish</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Wistar rat</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>semantic multi-classifier systems</value>
    </subject>
    <collection role="open_access" number="">open_access</collection>
    <collection role="persons" number="49455">Lausser, Ludwig</collection>
    <thesisPublisher>Technische Hochschule Ingolstadt</thesisPublisher>
    <file>https://opus4.kobv.de/opus4-haw/files/2730/biomolecules-08-00158-v2.pdf</file>
  </doc>
  <doc>
    <id>2728</id>
    <completedYear/>
    <publishedYear>2018</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst/>
    <pageLast/>
    <pageNumber>24</pageNumber>
    <edition/>
    <issue>3</issue>
    <volume>13</volume>
    <articleNumber>e0195126</articleNumber>
    <type>article</type>
    <publisherName>PLOS</publisherName>
    <publisherPlace>San Francisco</publisherPlace>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>0</belongsToBibliography>
    <completedDate>2022-08-22</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">A Boolean network of the crosstalk between IGF and Wnt signaling in aging satellite cells</title>
    <abstract language="eng">Aging is a complex biological process, which determines the life span of an organism. Insulin-like growth factor (IGF) and Wnt signaling pathways govern the process of aging. Both pathways share common downstream targets that allow competitive crosstalk between these branches. Of note, a shift from IGF to Wnt signaling has been observed during aging of satellite cells. Biological regulatory networks necessary to recreate aging have not yet been discovered. Here, we established a mathematical in silico model that robustly recapitulates the crosstalk between IGF and Wnt signaling. Strikingly, it predicts critical nodes following a shift from IGF to Wnt signaling. These findings indicate that this shift might cause age-related diseases.</abstract>
    <parentTitle language="eng">PLOS ONE</parentTitle>
    <identifier type="issn">1932-6203</identifier>
    <identifier type="urn">urn:nbn:de:bvb:573-27280</identifier>
    <enrichment key="THI_relatedIdentifier">https://doi.org/10.1371/journal.pone.0195126</enrichment>
    <enrichment key="THI_articleversion">published</enrichment>
    <enrichment key="THI_review">peer-review</enrichment>
    <enrichment key="THI_openaccess">ja</enrichment>
    <enrichment key="opus.source">publish</enrichment>
    <licence>Creative Commons BY 4.0</licence>
    <author>
      <first_name>Lea</first_name>
      <last_name>Kubis</last_name>
    </author>
    <author>
      <first_name>Julian D.</first_name>
      <last_name>Schwab</last_name>
    </author>
    <author>
      <first_name>Silke D.</first_name>
      <last_name>Werle</last_name>
    </author>
    <author>
      <first_name>Ludwig</first_name>
      <last_name>Lausser</last_name>
    </author>
    <author>
      <first_name>Stefan</first_name>
      <last_name>Tümpel</last_name>
    </author>
    <author>
      <first_name>Astrid S.</first_name>
      <last_name>Pfister</last_name>
    </author>
    <author>
      <first_name>Michael</first_name>
      <last_name>Kühl</last_name>
    </author>
    <author>
      <first_name>Hans A.</first_name>
      <last_name>Kestler</last_name>
    </author>
    <collection role="open_access" number="">open_access</collection>
    <collection role="persons" number="49455">Lausser, Ludwig</collection>
    <thesisPublisher>Technische Hochschule Ingolstadt</thesisPublisher>
    <file>https://opus4.kobv.de/opus4-haw/files/2728/file-1.pdf</file>
  </doc>
</export-example>
