<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Weinholdt C</submitter><funding>Bundesministerium für Bildung und Forschung</funding><funding>Deutsche Forschungsgemeinschaft</funding><funding>Deutsche Forschungsgemeinschaft (DE)</funding><funding>Bundesministerium für Bildung und Forschung (DE)</funding><pagination>434</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6704634</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The epidermal growth factor receptor (EGFR) is a major regulator of proliferation in tumor cells. Elevated expression levels of EGFR are associated with prognosis and clinical outcomes of patients in a variety of tumor types. There are at least four splice variants of the mRNA encoding four protein isoforms of EGFR in humans, named I through IV. EGFR isoform I is the full-length protein, whereas isoforms II-IV are shorter protein isoforms. Nevertheless, all EGFR isoforms bind the epidermal growth factor (EGF). Although EGFR is an essential target of long-established and successful tumor therapeutics, the exact function and biomarker potential of alternative EGFR isoforms II-IV are unclear, motivating more in-depth analyses. Hence, we analyzed transcriptome data from glio</pubmed_abstract><journal>BMC bioinformatics</journal><pubmed_title>Prediction of regulatory targets of alternative isoforms of the epidermal growth factor receptor in a glioblastoma cell line.</pubmed_title><pmcid>PMC6704634</pmcid><funding_grant_id>project number 251444481 - grant number GR 3526/6</funding_grant_id><funding_grant_id>project number 197267875 - grant number GR 3526/2</funding_grant_id><funding_grant_id>FKZ 24/19</funding_grant_id><funding_grant_id>FKZ: 16/18, 19/13, 21/25</funding_grant_id><pubmed_authors>Ardell DH</pubmed_authors><pubmed_authors>Grosse I</pubmed_authors><pubmed_authors>Kappler M</pubmed_authors><pubmed_authors>Kotrba J</pubmed_authors><pubmed_authors>Vordermark D</pubmed_authors><pubmed_authors>Eckert AW</pubmed_authors><pubmed_authors>Weinholdt C</pubmed_authors><pubmed_authors>Wichmann H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prediction of regulatory targets of alternative isoforms of the epidermal growth factor receptor in a glioblastoma cell line.</name><description>&lt;h4>Background&lt;/h4>The epidermal growth factor receptor (EGFR) is a major regulator of proliferation in tumor cells. Elevated expression levels of EGFR are associated with prognosis and clinical outcomes of patients in a variety of tumor types. There are at least four splice variants of the mRNA encoding four protein isoforms of EGFR in humans, named I through IV. EGFR isoform I is the full-length protein, whereas isoforms II-IV are shorter protein isoforms. Nevertheless, all EGFR isoforms bind the epidermal growth factor (EGF). Although EGFR is an essential target of long-established and successful tumor therapeutics, the exact function and biomarker potential of alternative EGFR isoforms II-IV are unclear, motivating more in-depth analyses. Hence, we analyzed transcriptome data from glio</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Aug</publication><modification>2026-05-01T04:49:13.821Z</modification><creation>2019-08-26T07:04:17Z</creation></dates><accession>S-EPMC6704634</accession><cross_references><pubmed>31438847</pubmed><doi>10.1186/s12859-019-2944-9</doi></cross_references></HashMap>