{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,28]],"date-time":"2026-09-28T18:55:35Z","timestamp":1790621735701,"version":"4.1.0"},"reference-count":9,"publisher":"Elsevier BV","issue":"10","license":[{"start":{"date-parts":[[2011,10,1]],"date-time":"2011-10-01T00:00:00Z","timestamp":1317427200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2011,10,1]],"date-time":"2011-10-01T00:00:00Z","timestamp":1317427200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2015,12,2]],"date-time":"2015-12-02T00:00:00Z","timestamp":1449014400000},"content-version":"vor","delay-in-days":1523,"URL":"http:\/\/www.elsevier.com\/open-access\/userlicense\/1.0\/"}],"content-domain":{"domain":["jidonline.org","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of Investigative Dermatology"],"published-print":{"date-parts":[[2011,10]]},"DOI":"10.1038\/jid.2011.166","type":"journal-article","created":{"date-parts":[[2011,7,7]],"date-time":"2011-07-07T08:47:07Z","timestamp":1310028427000},"page":"2131-2133","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":12,"title":["A New Case of Keratin 14 Functional Knockout Causes Severe Recessive EBS and Questions the Haploinsufficiency Model of Naegeli\u2013 Franceschetti\u2013 Jadassohn Syndrome"],"prefix":"10.1016","volume":"131","author":[{"given":"Matthias","family":"Titeux","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Audrey","family":"D\u00e9cha","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nathalie","family":"Pironon","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Laure","family":"Tonasso","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"G\u00e9raldine","family":"Gasc","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jos\u00e9 Enrique","family":"Mej\u00eda","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Catherine","family":"Prost-Squarcioni","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alain","family":"Hovnanian","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1038\/jid.2011.166_bb0010","doi-asserted-by":"crossref","first-page":"2574","DOI":"10.1101\/gad.8.21.2574","article-title":"A human keratin 14 \u201cknockout\u201d: the absence of K14 leads to severe epidermolysis bullosa simplex and a function for an intermediate filament protein","volume":"8","author":"Chan","year":"1994","journal-title":"Genes Dev"},{"key":"10.1038\/jid.2011.166_bb0015","doi-asserted-by":"crossref","first-page":"931","DOI":"10.1016\/j.jaad.2008.02.004","article-title":"The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB","volume":"58","author":"Fine","year":"2008","journal-title":"J Am Acad Dermatol"},{"issue":"Pt 3","key":"10.1038\/jid.2011.166_bb0020","doi-asserted-by":"crossref","first-page":"687","DOI":"10.1242\/jcs.101.3.687","article-title":"Interference in vimentin assembly in vitro by synthetic peptides derived from the vimentin head domain","volume":"101","author":"Hofmann","year":"1992","journal-title":"J Cell Sci"},{"key":"10.1038\/jid.2011.166_bb0025","doi-asserted-by":"crossref","first-page":"764","DOI":"10.1111\/1523-1747.ep12365805","article-title":"Effects of keratin 14 ablation on the clinical and cellular phenotype in a kindred with recessive epidermolysis bullosa simplex","volume":"107","author":"Jonkman","year":"1996","journal-title":"J Invest Dermatol"},{"key":"10.1038\/jid.2011.166_bb0030","doi-asserted-by":"crossref","first-page":"1484","DOI":"10.1126\/science.1138341","article-title":"RNA maps reveal new RNA classes and a possible function for pervasive transcription","volume":"316","author":"Kapranov","year":"2007","journal-title":"Science"},{"key":"10.1038\/jid.2011.166_bb0035","doi-asserted-by":"crossref","first-page":"1329","DOI":"10.1083\/jcb.129.5.1329","article-title":"The basal keratin network of stratified squamous epithelia: defining K15 function in the absence of K14","volume":"129","author":"Lloyd","year":"1995","journal-title":"J Cell Biol"},{"key":"10.1038\/jid.2011.166_bb0040","doi-asserted-by":"crossref","first-page":"724","DOI":"10.1086\/507792","article-title":"Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14","volume":"79","author":"Lugassy","year":"2006","journal-title":"Am J Hum Genet"},{"key":"10.1038\/jid.2011.166_bb0045","doi-asserted-by":"crossref","first-page":"1517","DOI":"10.1038\/sj.jid.5701187","article-title":"KRT14 haploinsufficiency results in increased susceptibility of keratinocytes to TNF-alpha-induced apoptosis and causes Naegeli-Franceschetti-Jadassohn syndrome","volume":"128","author":"Lugassy","year":"2008","journal-title":"J Invest Dermatol"},{"key":"10.1038\/jid.2011.166_bb0050","doi-asserted-by":"crossref","first-page":"278","DOI":"10.1016\/S0168-9525(03)00071-4","article-title":"Phenotypes, genotypes and their contribution to understanding keratin function","volume":"19","author":"Porter","year":"2003","journal-title":"Trends Genet"}],"container-title":["Journal of Investigative Dermatology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022202X15350569?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022202X15350569?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,4,3]],"date-time":"2025-04-03T06:28:03Z","timestamp":1743661683000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0022202X15350569"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2011,10]]},"references-count":9,"journal-issue":{"issue":"10","published-print":{"date-parts":[[2011,10]]}},"alternative-id":["S0022202X15350569"],"URL":"https:\/\/doi.org\/10.1038\/jid.2011.166","relation":{},"ISSN":["0022-202X"],"issn-type":[{"value":"0022-202X","type":"print"}],"subject":[],"published":{"date-parts":[[2011,10]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"A New Case of Keratin 14 Functional Knockout Causes Severe Recessive EBS and Questions the Haploinsufficiency Model of Naegeli\u2013Franceschetti\u2013Jadassohn Syndrome","name":"articletitle","label":"Article Title"},{"value":"Journal of Investigative Dermatology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1038\/jid.2011.166","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"simple-article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2011 The Society for Investigative Dermatology, Inc. Published by Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies.","name":"copyright","label":"Copyright"}]}}