{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,10,31]],"date-time":"2023-10-31T00:44:19Z","timestamp":1698713059172},"reference-count":10,"publisher":"Elsevier BV","issue":"1","license":[{"start":{"date-parts":[[2008,10,1]],"date-time":"2008-10-01T00:00:00Z","timestamp":1222819200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Journal of Dermatological Science"],"published-print":{"date-parts":[[2008,10]]},"DOI":"10.1016\/j.jdermsci.2008.05.005","type":"journal-article","created":{"date-parts":[[2008,7,19]],"date-time":"2008-07-19T08:47:22Z","timestamp":1216457242000},"page":"55-57","source":"Crossref","is-referenced-by-count":5,"title":["Common NOD2 mutations are rare in patients with inverse acne"],"prefix":"10.1016","volume":"52","author":[{"given":"Sylke","family":"Schneider-Burrus","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Daniela","family":"Meixner","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Wolfram","family":"Sterry","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ansgar","family":"Lukowsky","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.jdermsci.2008.05.005_bib1","doi-asserted-by":"crossref","first-page":"599","DOI":"10.1038\/35079107","article-title":"Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease","volume":"411","author":"Hugot","year":"2001","journal-title":"Nature"},{"key":"10.1016\/j.jdermsci.2008.05.005_bib2","doi-asserted-by":"crossref","first-page":"1925","DOI":"10.1016\/S0140-6736(00)05063-7","article-title":"Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations","volume":"357","author":"Hampe","year":"2001","journal-title":"Lancet"},{"key":"10.1016\/j.jdermsci.2008.05.005_bib3","doi-asserted-by":"crossref","first-page":"603","DOI":"10.1038\/35079114","article-title":"A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease","volume":"411","author":"Ogura","year":"2001","journal-title":"Nature"},{"key":"10.1016\/j.jdermsci.2008.05.005_bib4","doi-asserted-by":"crossref","first-page":"44","DOI":"10.1002\/humu.20264","article-title":"Mutation, selection, and evolution of the Crohn disease susceptibility gene CARD15","volume":"27","author":"King","year":"2006","journal-title":"Hum Mutat"},{"key":"10.1016\/j.jdermsci.2008.05.005_bib5","doi-asserted-by":"crossref","first-page":"845","DOI":"10.1086\/339432","article-title":"CARD15\/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease","volume":"70","author":"Lesage","year":"2002","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.jdermsci.2008.05.005_bib6","doi-asserted-by":"crossref","first-page":"2005","DOI":"10.1074\/jbc.M511044200","article-title":"NOD2\/CARD15 mediates induction of the antimicrobial peptide human beta-defensin-2","volume":"281","author":"Voss","year":"2006","journal-title":"J Biol Chem"},{"key":"10.1016\/j.jdermsci.2008.05.005_bib7","doi-asserted-by":"crossref","first-page":"19","DOI":"10.1038\/ng720","article-title":"CARD15 mutations in Blau syndrome","volume":"29","author":"Miceli-Richard","year":"2001","journal-title":"Nat Genet"},{"key":"10.1016\/j.jdermsci.2008.05.005_bib8","doi-asserted-by":"crossref","first-page":"359","DOI":"10.1159\/000107632","article-title":"Lack of association between CARD15 gene polymorphisms and hidradenitis suppurativa: a pilot study","volume":"215","author":"Nassar","year":"2007","journal-title":"Dermatology"},{"key":"10.1016\/j.jdermsci.2008.05.005_bib9","doi-asserted-by":"crossref","first-page":"1235","DOI":"10.1080\/00365520310006612","article-title":"Prevalence of mutations of the NOD2\/CARD15 gene and relation to phenotype in Spanish patients with Crohn disease","volume":"38","author":"Mendoza","year":"2003","journal-title":"Scand J Gastroenterol"},{"key":"10.1016\/j.jdermsci.2008.05.005_bib10","doi-asserted-by":"crossref","DOI":"10.1111\/j.1572-0241.2007.01149.x","article-title":"Prevalence of CARD15\/NOD2 Mutations in Caucasian Healthy People","author":"Hugot","year":"2007","journal-title":"Am J Gastroenterol"}],"container-title":["Journal of Dermatological Science"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0923181108001746?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0923181108001746?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2018,12,27]],"date-time":"2018-12-27T04:50:50Z","timestamp":1545886250000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0923181108001746"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2008,10]]},"references-count":10,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2008,10]]}},"alternative-id":["S0923181108001746"],"URL":"https:\/\/doi.org\/10.1016\/j.jdermsci.2008.05.005","relation":{},"ISSN":["0923-1811"],"issn-type":[{"value":"0923-1811","type":"print"}],"subject":[],"published":{"date-parts":[[2008,10]]}}}