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http://purl.uniprot.org/citations/21811097http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/21811097http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/21811097http://www.w3.org/2000/01/rdf-schema#comment"Alternative splicing is a central tool  of evolution that significantly increases the size of transcriptomes and generates functional specification. Within the human ERBB receptor gene family, only ERBB4 is known to produce functionally distinct isoforms as a result of alternative splicing. While ErbB4 signaling has been demonstrated to regulate cellular processes involved in embryogenesis, carcinogenesis and cardiovascular and psychiatric diseases, relatively little is known about the contribution of the individual isoforms in the different biological contexts. Here, we review recent findings as well as provide novel data about the distribution and functions of the ERBB4 splice variants. These observations represent an example of how minor alterations in the transcripts of a single gene can result in even antagonistic cellular responses. The observations also underline the significance of understanding the unique functions of isoforms of a potential drug target gene."xsd:string
http://purl.uniprot.org/citations/21811097http://purl.org/dc/terms/identifier"doi:10.4161/cc.10.16.17194"xsd:string
http://purl.uniprot.org/citations/21811097http://purl.org/dc/terms/identifier"doi:10.4161/cc.10.16.17194"xsd:string
http://purl.uniprot.org/citations/21811097http://purl.uniprot.org/core/author"Sundvall M."xsd:string
http://purl.uniprot.org/citations/21811097http://purl.uniprot.org/core/author"Sundvall M."xsd:string
http://purl.uniprot.org/citations/21811097http://purl.uniprot.org/core/author"Iljin K."xsd:string
http://purl.uniprot.org/citations/21811097http://purl.uniprot.org/core/author"Iljin K."xsd:string
http://purl.uniprot.org/citations/21811097http://purl.uniprot.org/core/author"Elenius K."xsd:string
http://purl.uniprot.org/citations/21811097http://purl.uniprot.org/core/author"Elenius K."xsd:string
http://purl.uniprot.org/citations/21811097http://purl.uniprot.org/core/author"Halkilahti K."xsd:string
http://purl.uniprot.org/citations/21811097http://purl.uniprot.org/core/author"Halkilahti K."xsd:string
http://purl.uniprot.org/citations/21811097http://purl.uniprot.org/core/author"Vaparanta K."xsd:string
http://purl.uniprot.org/citations/21811097http://purl.uniprot.org/core/author"Vaparanta K."xsd:string
http://purl.uniprot.org/citations/21811097http://purl.uniprot.org/core/author"Veikkolainen V."xsd:string
http://purl.uniprot.org/citations/21811097http://purl.uniprot.org/core/author"Veikkolainen V."xsd:string
http://purl.uniprot.org/citations/21811097http://purl.uniprot.org/core/date"2011"xsd:gYear
http://purl.uniprot.org/citations/21811097http://purl.uniprot.org/core/date"2011"xsd:gYear
http://purl.uniprot.org/citations/21811097http://purl.uniprot.org/core/name"Cell Cycle"xsd:string
http://purl.uniprot.org/citations/21811097http://purl.uniprot.org/core/name"Cell Cycle"xsd:string
http://purl.uniprot.org/citations/21811097http://purl.uniprot.org/core/pages"2647-2657"xsd:string
http://purl.uniprot.org/citations/21811097http://purl.uniprot.org/core/pages"2647-2657"xsd:string
http://purl.uniprot.org/citations/21811097http://purl.uniprot.org/core/title"Function of ERBB4 is determined by alternative splicing."xsd:string
http://purl.uniprot.org/citations/21811097http://purl.uniprot.org/core/title"Function of ERBB4 is determined by alternative splicing."xsd:string