{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,4]],"date-time":"2026-05-04T15:15:13Z","timestamp":1777907713946,"version":"3.51.4"},"reference-count":6,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2025,4,1]],"date-time":"2025-04-01T00:00:00Z","timestamp":1743465600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2025,4,1]],"date-time":"2025-04-01T00:00:00Z","timestamp":1743465600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2025,2,12]],"date-time":"2025-02-12T00:00:00Z","timestamp":1739318400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"funder":[{"DOI":"10.13039\/100008909","name":"Once Upon A Time Foundation","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100008909","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100001466","name":"American Urological Association Foundation","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100001466","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000062","name":"National Institute of Diabetes and Digestive and Kidney Diseases","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100000062","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Stem Cell Research"],"published-print":{"date-parts":[[2025,4]]},"DOI":"10.1016\/j.scr.2025.103681","type":"journal-article","created":{"date-parts":[[2025,2,13]],"date-time":"2025-02-13T03:19:49Z","timestamp":1739416789000},"page":"103681","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":1,"special_numbering":"C","title":["Generation of induced pluripotent stem cell line, NCHi028-A, from a male child with Prune Belly Syndrome"],"prefix":"10.1016","volume":"84","author":[{"given":"Cintia E.","family":"Gomez Limia","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Karunya","family":"Albert","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kusum","family":"Basnet","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Chaitrali","family":"Atre","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hudaa","family":"Malik","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Darria L.","family":"Streeter","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nathalia G.","family":"Amado","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-8272-4886","authenticated-orcid":false,"given":"Linda A.","family":"Baker","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"1","key":"10.1016\/j.scr.2025.103681_b0005","doi-asserted-by":"crossref","first-page":"339","DOI":"10.1038\/s41467-023-44594-0","article-title":"PIEZO1 loss-of-function compound heterozygous mutations in the rare congenital human disorder Prune Belly Syndrome","volume":"15","author":"Amado","year":"2024","journal-title":"Nat Commun."},{"key":"10.1016\/j.scr.2025.103681_b0010","doi-asserted-by":"crossref","first-page":"16","DOI":"10.1016\/j.scr.2017.08.006","article-title":"Generation and characterization of a human induced pluripotent stem (iPS) cell line derived from an acute myeloid leukemia patient evolving from primary myelofibrosis carrying the CALR 52bp deletion and the ASXL1 p.R693X mutation","volume":"24","author":"Gomez Limia","year":"2017","journal-title":"Stem Cell Res."},{"issue":"1","key":"10.1016\/j.scr.2025.103681_b0015","doi-asserted-by":"crossref","first-page":"272","DOI":"10.1016\/j.juro.2011.09.036","article-title":"Genetic basis of prune belly syndrome: screening for HNF1\u03b2 gene","volume":"187","author":"Granberg","year":"2012","journal-title":"J Urol."},{"issue":"5","key":"10.1016\/j.scr.2025.103681_b0020","doi-asserted-by":"crossref","DOI":"10.1016\/j.jpurol.2015.06.005","article-title":"Impact and frequency of extra-genitourinary manifestations of prune belly syndrome","volume":"11","author":"Grimsby","year":"2015","journal-title":"J Pediatr Urol."},{"issue":"4","key":"10.1016\/j.scr.2025.103681_b0025","doi-asserted-by":"crossref","first-page":"548","DOI":"10.1016\/j.jpurol.2021.04.010","article-title":"Modern management of and update on prune belly syndrome","volume":"17","author":"Lopes","year":"2021","journal-title":"J Pediatr Urol."},{"issue":"1","key":"10.1016\/j.scr.2025.103681_b0030","doi-asserted-by":"crossref","first-page":"130","DOI":"10.1111\/bju.14524","article-title":"Phenotypic severity scoring system and categorisation for prune belly syndrome: application to a pilot cohort of 50 living patients","volume":"123","author":"Wong","year":"2019","journal-title":"BJU Int."}],"container-title":["Stem Cell Research"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1873506125000315?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1873506125000315?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2026,5,1]],"date-time":"2026-05-01T13:45:29Z","timestamp":1777643129000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1873506125000315"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,4]]},"references-count":6,"alternative-id":["S1873506125000315"],"URL":"https:\/\/doi.org\/10.1016\/j.scr.2025.103681","relation":{},"ISSN":["1873-5061"],"issn-type":[{"value":"1873-5061","type":"print"}],"subject":[],"published":{"date-parts":[[2025,4]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Generation of induced pluripotent stem cell line, NCHi028-A, from a male child with Prune Belly Syndrome","name":"articletitle","label":"Article Title"},{"value":"Stem Cell Research","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.scr.2025.103681","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2025 The Authors. Published by Elsevier B.V.","name":"copyright","label":"Copyright"}],"article-number":"103681"}}