{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,9]],"date-time":"2026-03-09T20:36:56Z","timestamp":1773088616581,"version":"3.50.1"},"reference-count":23,"publisher":"Elsevier BV","issue":"2","license":[{"start":{"date-parts":[[2011,4,1]],"date-time":"2011-04-01T00:00:00Z","timestamp":1301616000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2011,4,1]],"date-time":"2011-04-01T00:00:00Z","timestamp":1301616000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Annales d'Endocrinologie"],"published-print":{"date-parts":[[2011,4]]},"DOI":"10.1016\/j.ando.2011.03.011","type":"journal-article","created":{"date-parts":[[2011,4,22]],"date-time":"2011-04-22T15:15:20Z","timestamp":1303485320000},"page":"95-98","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":24,"title":["Inherited defects of thyroid hormone metabolism"],"prefix":"10.1016","volume":"72","author":[{"given":"A.M.","family":"Dumitrescu","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S.","family":"Refetoff","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.ando.2011.03.011_bib0005","doi-asserted-by":"crossref","first-page":"17","DOI":"10.1146\/annurev.nutr.23.011702.073318","article-title":"Mechanism and regulation of selenoprotein synthesis","volume":"23","author":"Driscoll","year":"2003","journal-title":"Annu Rev Nutr"},{"issue":"5","key":"10.1016\/j.ando.2011.03.011_bib0010","doi-asserted-by":"crossref","first-page":"408","DOI":"10.1038\/nsmb922","article-title":"Ribosomal protein L30 is a component of the UGA-selenocysteine recoding machinery in eukaryotes","volume":"12","author":"Chavatte","year":"2005","journal-title":"Nat Struct Mol Biol"},{"issue":"7","key":"10.1016\/j.ando.2011.03.011_bib0015","doi-asserted-by":"crossref","first-page":"5542","DOI":"10.1074\/jbc.M411725200","article-title":"Selective rescue of selenoprotein expression in mice lacking a highly specialized methyl group in selenocysteine tRNA","volume":"280","author":"Carlson","year":"2005","journal-title":"J Biol Chem"},{"issue":"7","key":"10.1016\/j.ando.2011.03.011_bib0020","doi-asserted-by":"crossref","first-page":"775","DOI":"10.1089\/ars.2007.1528","article-title":"From selenium to selenoproteins: synthesis, identity, and their role in human health","volume":"9","author":"Papp","year":"2007","journal-title":"Antioxid Redox Signal"},{"issue":"1","key":"10.1016\/j.ando.2011.03.011_bib0025","doi-asserted-by":"crossref","first-page":"11","DOI":"10.1042\/BJ20090219","article-title":"Regulation, function of selenoproteins in human disease","volume":"422","author":"Bellinger","year":"2009","journal-title":"Biochem J"},{"issue":"2","key":"10.1016\/j.ando.2011.03.011_bib0030","doi-asserted-by":"crossref","first-page":"306","DOI":"10.1093\/emboj\/19.2.306","article-title":"A novel RNA binding protein, SBP2, is required for the translation of mammalian selenoprotein mRNAs","volume":"19","author":"Copeland","year":"2000","journal-title":"Embo J"},{"issue":"5624","key":"10.1016\/j.ando.2011.03.011_bib0035","doi-asserted-by":"crossref","first-page":"1439","DOI":"10.1126\/science.1083516","article-title":"Characterization of mammalian selenoproteomes","volume":"300","author":"Kryukov","year":"2003","journal-title":"Science"},{"issue":"11","key":"10.1016\/j.ando.2011.03.011_bib0040","doi-asserted-by":"crossref","first-page":"5531","DOI":"10.1073\/pnas.94.11.5531","article-title":"Early embryonic lethality caused by targeted disruption of the mouse selenocysteine tRNA gene (Trsp)","volume":"94","author":"Bosl","year":"1997","journal-title":"Proc Natl Acad Sci U.S.A"},{"issue":"Pt 3","key":"10.1016\/j.ando.2011.03.011_bib0045","doi-asserted-by":"crossref","first-page":"851","DOI":"10.1042\/bj3570851","article-title":"Selenium regulation of transcript abundance and translational efficiency of glutathione peroxidase-1 and -4 in rat liver","volume":"357","author":"Weiss Sachdev","year":"2001","journal-title":"Biochem J"},{"issue":"48","key":"10.1016\/j.ando.2011.03.011_bib0050","doi-asserted-by":"crossref","first-page":"34653","DOI":"10.1074\/jbc.M707059200","article-title":"Altered RNA binding activity underlies abnormal thyroid hormone metabolism linked to a mutation in selenocysteine insertion sequence-binding protein 2","volume":"282","author":"Bubenik","year":"2007","journal-title":"J Biol Chem"},{"issue":"22","key":"10.1016\/j.ando.2011.03.011_bib0055","doi-asserted-by":"crossref","first-page":"7848","DOI":"10.1128\/MCB.00793-07","article-title":"SBP2 binding affinity is a major determinant in differential selenoprotein mRNA translation and sensitivity to nonsense-mediated decay","volume":"27","author":"Squires","year":"2007","journal-title":"Mol Cell Biol"},{"issue":"11","key":"10.1016\/j.ando.2011.03.011_bib0060","doi-asserted-by":"crossref","first-page":"1247","DOI":"10.1038\/ng1654","article-title":"Mutations in SECISBP2 result in abnormal thyroid hormone metabolism","volume":"37","author":"Dumitrescu","year":"2005","journal-title":"Nat Genet"},{"key":"10.1016\/j.ando.2011.03.011_bib0065","doi-asserted-by":"crossref","unstructured":"Di Cosmo C, McLellan N, Liao XH, et al. Clinical and molecular characterization of a novel selenocysteine insertion sequence-binding protein 2 (SBP2) gene mutation (R128X). J Clin Endocrinol Metab 2009;94(10):4003\u20139.","DOI":"10.1210\/jc.2009-0686"},{"key":"10.1016\/j.ando.2011.03.011_bib0070","doi-asserted-by":"crossref","unstructured":"Azevedo MF, Barra GB, Naves LA, et al. Selenoprotein-related disease in a young girl caused by nonsense mutations in the SBP2 gene. J Clin Endocrinol Metab 2010;95(8):4066\u20134071.","DOI":"10.1210\/jc.2009-2611"},{"key":"10.1016\/j.ando.2011.03.011_bib0075","doi-asserted-by":"crossref","unstructured":"Schoenmakers E, Agostini M, Mitchell C, et al. Mutations in the selenocysteine insertion sequence-binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humans. J Clin Invest 2010;120(12):4220\u20134235.","DOI":"10.1172\/JCI43653"},{"issue":"1\u20132","key":"10.1016\/j.ando.2011.03.011_bib0080","doi-asserted-by":"crossref","first-page":"279","DOI":"10.1016\/S0378-1119(02)00629-7","article-title":"cDNA cloning, expression pattern and RNA binding analysis of human selenocysteine insertion sequence (SECIS) binding protein 2","volume":"291","author":"Lescure","year":"2002","journal-title":"Gene"},{"key":"10.1016\/j.ando.2011.03.011_bib0085","doi-asserted-by":"crossref","first-page":"17","DOI":"10.1016\/S0378-1119(03)00588-2","article-title":"Regulation of gene expression by stop codon recoding: selenocysteine","volume":"312","author":"Copeland","year":"2003","journal-title":"Gene"},{"issue":"13","key":"10.1016\/j.ando.2011.03.011_bib0090","doi-asserted-by":"crossref","first-page":"4895","DOI":"10.1128\/MCB.02284-05","article-title":"The redox state of SECIS binding protein 2 controls its localization and selenocysteine incorporation function","volume":"26","author":"Papp","year":"2006","journal-title":"Mol Cell Biol"},{"issue":"10","key":"10.1016\/j.ando.2011.03.011_bib0095","first-page":"1442","article-title":"The selenocysteine incorporation machinery: interactions between the SECIS RNA and the SECIS-binding protein SBP2","volume":"7","author":"Fletcher","year":"2001","journal-title":"Rna"},{"key":"10.1016\/j.ando.2011.03.011_bib0100","doi-asserted-by":"crossref","unstructured":"Dumitrescu AM, Di Cosmo C, Liao XH, Weiss RE, Refetoff S. The syndrome of inherited partial SBP2 deficiency in humans. Antioxid Redox Signal 2010;12(7):905\u2013920","DOI":"10.1089\/ars.2009.2892"},{"issue":"3","key":"10.1016\/j.ando.2011.03.011_bib0105","doi-asserted-by":"crossref","first-page":"277","DOI":"10.1089\/thy.2008.0397","article-title":"Selenium supplementation fails to correct the selenoprotein synthesis defect in subjects with SBP2 gene mutations","volume":"19","author":"Schomburg","year":"2009","journal-title":"Thyroid"},{"issue":"4","key":"10.1016\/j.ando.2011.03.011_bib0110","doi-asserted-by":"crossref","first-page":"804","DOI":"10.1158\/1055-9965.EPI-05-0950","article-title":"Effects of chemical form of selenium on plasma biomarkers in a high-dose human supplementation trial","volume":"15","author":"Burk","year":"2006","journal-title":"Cancer Epidemiol Biomarkers Prev"},{"issue":"1","key":"10.1016\/j.ando.2011.03.011_bib0115","doi-asserted-by":"crossref","first-page":"e4","DOI":"10.1371\/journal.pbio.0050004","article-title":"Biosynthesis of selenocysteine on its tRNA in eukaryotes","volume":"5","author":"Xu","year":"2007","journal-title":"PLoS Biol"}],"container-title":["Annales d'Endocrinologie"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0003426611000382?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0003426611000382?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,9,12]],"date-time":"2025-09-12T22:45:09Z","timestamp":1757717109000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0003426611000382"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2011,4]]},"references-count":23,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2011,4]]}},"alternative-id":["S0003426611000382"],"URL":"https:\/\/doi.org\/10.1016\/j.ando.2011.03.011","relation":{},"ISSN":["0003-4266"],"issn-type":[{"value":"0003-4266","type":"print"}],"subject":[],"published":{"date-parts":[[2011,4]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Inherited defects of thyroid hormone metabolism","name":"articletitle","label":"Article Title"},{"value":"Annales d'Endocrinologie","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.ando.2011.03.011","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2011 Elsevier Masson SAS. All rights reserved.","name":"copyright","label":"Copyright"}]}}