<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(2)</volume><submitter>Lei KE</submitter><pubmed_abstract>Ectodysplasin (&lt;i>EDA&lt;/i>) gene mutation is associated with hypohidrotic ectodermal dysplasia (HED). The aim of this study was to investigate the effect of ectodysplasin, transcript variant 1 (EDA-A1) on the proliferation and cell cycle of ECV304 human umbilical vein endothelial cells (HUVECs). Recombinant eukaryotic expression vectors containing mutant (M) and wild-type (W) &lt;i>EDA-A1&lt;/i> coding sequences, pcDNA3.1 (-)-EDA-A1-M and pcDNA3.1 (-)-EDA-A1-W, respectively, were transfected into ECV304 cells. The EDA-A1 gene was amplified by reverse transcription polymerase chain reaction (RT-PCR), and the protein was detected by western blotting. The EDA-A1 gene and protein were detected in ECV304 cells transfected with pcDNA3.1 (-)-EDA-A1-M and pcDNA3.1 (-)-EDA-A1-W, but not in ECV304 cells tr</pubmed_abstract><journal>Experimental and therapeutic medicine</journal><pagination>535-539</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4734069</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Effect of an &lt;i>EDA-A1&lt;/i> gene mutant on the proliferation and cell cycle distribution of cultured human umbilical vein endothelial cells.</pubmed_title><pmcid>PMC4734069</pmcid><pubmed_authors>Ma B</pubmed_authors><pubmed_authors>Che T</pubmed_authors><pubmed_authors>Lei KE</pubmed_authors><pubmed_authors>Shi P</pubmed_authors><pubmed_authors>He X</pubmed_authors><pubmed_authors>Li L</pubmed_authors><pubmed_authors>Wang L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Effect of an &lt;i>EDA-A1&lt;/i> gene mutant on the proliferation and cell cycle distribution of cultured human umbilical vein endothelial cells.</name><description>Ectodysplasin (&lt;i>EDA&lt;/i>) gene mutation is associated with hypohidrotic ectodermal dysplasia (HED). The aim of this study was to investigate the effect of ectodysplasin, transcript variant 1 (EDA-A1) on the proliferation and cell cycle of ECV304 human umbilical vein endothelial cells (HUVECs). Recombinant eukaryotic expression vectors containing mutant (M) and wild-type (W) &lt;i>EDA-A1&lt;/i> coding sequences, pcDNA3.1 (-)-EDA-A1-M and pcDNA3.1 (-)-EDA-A1-W, respectively, were transfected into ECV304 cells. The EDA-A1 gene was amplified by reverse transcription polymerase chain reaction (RT-PCR), and the protein was detected by western blotting. The EDA-A1 gene and protein were detected in ECV304 cells transfected with pcDNA3.1 (-)-EDA-A1-M and pcDNA3.1 (-)-EDA-A1-W, but not in ECV304 cells tr</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Feb</publication><modification>2025-04-04T20:26:06.562Z</modification><creation>2019-03-27T02:07:56Z</creation></dates><accession>S-EPMC4734069</accession><cross_references><pubmed>26893642</pubmed><doi>10.3892/etm.2015.2952</doi></cross_references></HashMap>