{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T04:38:03Z","timestamp":1791261483585,"version":"4.1.0"},"reference-count":0,"publisher":"Oxford University Press (OUP)","issue":"23","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2002,11,1]]},"DOI":"10.1093\/hmg\/11.23.2951","type":"journal-article","created":{"date-parts":[[2002,10,22]],"date-time":"2002-10-22T17:06:19Z","timestamp":1035306379000},"page":"2951-2960","source":"Crossref","is-referenced-by-count":79,"title":["Targeted disruption of Slc19a2, the gene encoding the high-affinity thiamin transporter Thtr-1, causes diabetes mellitus, sensorineural deafness and megaloblastosis in mice"],"prefix":"10.1093","volume":"11","author":[{"given":"K.","family":"Oishi","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"286","container-title":["Human Molecular Genetics"],"original-title":[],"link":[{"URL":"http:\/\/academic.oup.com\/hmg\/article-pdf\/11\/23\/2951\/1798631\/ddf291.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2017,8,23]],"date-time":"2017-08-23T08:48:06Z","timestamp":1503478086000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/hmg\/article-lookup\/doi\/10.1093\/hmg\/11.23.2951"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2002,11,1]]},"references-count":0,"journal-issue":{"issue":"23"},"URL":"https:\/\/doi.org\/10.1093\/hmg\/11.23.2951","relation":{},"ISSN":["1460-2083"],"issn-type":[{"value":"1460-2083","type":"electronic"}],"subject":[],"published":{"date-parts":[[2002,11,1]]}}}