{"doi":"10.1016/j.scr.2019.101679","title":"Induced pluripotent stem cell line (PEIi003-A) derived from an apparently healthy male individual","abstract":null,"journal":"Stem Cell Research","year":2020,"id":683343,"datarank":0.16479184330021646,"base_score":1.0986122886681096,"endowment":1.0986122886681096,"self_citation_contribution":0.16479184330021646,"citation_network_contribution":0.0,"self_endowment_contribution":0.16479184330021646,"citer_contribution":0.0,"corpus_percentile":null,"corpus_rank":null,"citation_count":2,"citer_count":0,"citers_with_citation_signal":0,"citers_with_endowment":0,"datacite_reuse_total":0,"is_dataset":false,"is_dataset_confidence":null,"is_data_producer":false,"deposit_databanks":null,"is_oa":false,"file_count":0,"downloads":0,"has_version_chain":false,"published_date":null,"fair_score":null,"fair_percentile":null,"algorithm_id":"datarank_citation_only_1hop_v6","ranking_scope":"data_only","authors":[{"id":378572,"name":"Maximilian Schieck","orcid":"0000-0001-5878-0546","position":1,"is_corresponding":false},{"id":1785119,"name":"Michaela Neuenkirch","orcid":null,"position":2,"is_corresponding":false},{"id":1785120,"name":"Christiane Tondera","orcid":null,"position":3,"is_corresponding":false},{"id":1785121,"name":"Heike Schmitz","orcid":null,"position":4,"is_corresponding":false},{"id":1441478,"name":"Doris Steinemann","orcid":"0000-0001-8797-0816","position":5,"is_corresponding":false},{"id":50607,"name":"Gudrun Göhring","orcid":"0000-0002-0863-8645","position":6,"is_corresponding":false},{"id":295384,"name":"Renate König","orcid":"0000-0003-4882-9179","position":7,"is_corresponding":false},{"id":866154,"name":"Nina V. Fuchs","orcid":"0000-0003-4175-0740","position":0,"is_corresponding":false}],"reference_count":0,"raw_metadata":{"has_enrichment":true,"resolved":true,"title":"Induced pluripotent stem cell line (PEIi003-A) derived from an apparently healthy male individual","abstract":"Induced pluripotent stem cells (iPSCs) are a useful tool to investigate pathomechanistic and cellular processes due to their differentiation potential into different somatic cell types in vitro. Here, we have generated iPSCs from an apparently healthy male individual using an integration-free reprogramming method. The resulting iPSCs are pluripotent and display a normal karyotype. 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