Publikation: Integrin-β4 is a novel transcriptional target of TAp73
Dateien
Datum
Autor:innen
Herausgeber:innen
ISSN der Zeitschrift
Electronic ISSN
ISBN
Bibliografische Daten
Verlag
Schriftenreihe
Auflagebezeichnung
DOI (zitierfähiger Link)
Internationale Patentnummer
Angaben zur Forschungsförderung
Projekt
Open Access-Veröffentlichung
Sammlungen
Core Facility der Universität Konstanz
Titel in einer weiteren Sprache
Publikationstyp
Publikationsstatus
Erschienen in
Zusammenfassung
As a member of p53 family, p73 has attracted intense investigations due to its structural and functional similarities to p53. Among more than ten p73 variants, the transactivation (TA) domain-containing isoform TAp73 is the one that imitates the p53's behavior most. TAp73 induces apoptosis and cell cycle arrest, which endows it the capacity of tumour suppression. Also, it can exert diverse biological influences on cells through activating a complex and context dependent transcriptional programme. The transcriptional activities further broaden its roles in more intricate biological processes. In this article, we report that p73 is a positive regulator of a cell adhesion related gene named integrin β4 (ITGB4). This finding may have implications for the dissection of the biological mechanisms underlining p73 functions.
Zusammenfassung in einer weiteren Sprache
Fachgebiet (DDC)
Schlagwörter
Konferenz
Rezension
Zitieren
ISO 690
XIE, Ningxia, Polina VIKHREVA, Margherita ANNICCHIARICO-PETRUZZELLI, Ivano AMELIO, Nicolai BARLEV, Richard A. KNIGHT, Gerry MELINO, 2018. Integrin-β4 is a novel transcriptional target of TAp73. In: Cell Cycle. Taylor & Francis. 2018, 17(5), pp. 589-594. ISSN 1538-4101. eISSN 1551-4005. Available under: doi: 10.1080/15384101.2017.1403684BibTex
@article{Xie2018Integ-56665, year={2018}, doi={10.1080/15384101.2017.1403684}, title={Integrin-β4 is a novel transcriptional target of TAp73}, number={5}, volume={17}, issn={1538-4101}, journal={Cell Cycle}, pages={589--594}, author={Xie, Ningxia and Vikhreva, Polina and Annicchiarico-Petruzzelli, Margherita and Amelio, Ivano and Barlev, Nicolai and Knight, Richard A. and Melino, Gerry} }
RDF
<rdf:RDF xmlns:dcterms="http://purl.org/dc/terms/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:bibo="http://purl.org/ontology/bibo/" xmlns:dspace="http://digital-repositories.org/ontologies/dspace/0.1.0#" xmlns:foaf="http://xmlns.com/foaf/0.1/" xmlns:void="http://rdfs.org/ns/void#" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > <rdf:Description rdf:about="https://kops.uni-konstanz.de/server/rdf/resource/123456789/56665"> <dc:contributor>Melino, Gerry</dc:contributor> <dc:creator>Melino, Gerry</dc:creator> <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/28"/> <dc:rights>terms-of-use</dc:rights> <foaf:homepage rdf:resource="http://localhost:8080/"/> <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/28"/> <dc:creator>Vikhreva, Polina</dc:creator> <bibo:uri rdf:resource="https://kops.uni-konstanz.de/handle/123456789/56665"/> <dc:contributor>Amelio, Ivano</dc:contributor> <dc:creator>Knight, Richard A.</dc:creator> <dc:creator>Xie, Ningxia</dc:creator> <dc:contributor>Barlev, Nicolai</dc:contributor> <dc:contributor>Knight, Richard A.</dc:contributor> <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2022-02-23T13:00:15Z</dcterms:available> <dc:contributor>Vikhreva, Polina</dc:contributor> <dcterms:issued>2018</dcterms:issued> <dcterms:rights rdf:resource="https://rightsstatements.org/page/InC/1.0/"/> <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2022-02-23T13:00:15Z</dc:date> <dc:contributor>Xie, Ningxia</dc:contributor> <dc:creator>Annicchiarico-Petruzzelli, Margherita</dc:creator> <dc:creator>Amelio, Ivano</dc:creator> <dcterms:title>Integrin-β4 is a novel transcriptional target of TAp73</dcterms:title> <dc:contributor>Annicchiarico-Petruzzelli, Margherita</dc:contributor> <void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/> <dc:creator>Barlev, Nicolai</dc:creator> <dcterms:abstract xml:lang="eng">As a member of p53 family, p73 has attracted intense investigations due to its structural and functional similarities to p53. Among more than ten p73 variants, the transactivation (TA) domain-containing isoform TAp73 is the one that imitates the p53's behavior most. TAp73 induces apoptosis and cell cycle arrest, which endows it the capacity of tumour suppression. Also, it can exert diverse biological influences on cells through activating a complex and context dependent transcriptional programme. The transcriptional activities further broaden its roles in more intricate biological processes. In this article, we report that p73 is a positive regulator of a cell adhesion related gene named integrin β4 (ITGB4). This finding may have implications for the dissection of the biological mechanisms underlining p73 functions.</dcterms:abstract> <dc:language>eng</dc:language> </rdf:Description> </rdf:RDF>