{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,3]],"date-time":"2026-09-03T14:40:54Z","timestamp":1788446454322,"version":"build-2803163510"},"reference-count":35,"publisher":"Wiley","issue":"8","license":[{"start":{"date-parts":[[2015,2,6]],"date-time":"2015-02-06T00:00:00Z","timestamp":1423180800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"name":"Foundation for Medical Research of the Tri-Service General Hospital","award":["TSGH-C101-066"],"award-info":[{"award-number":["TSGH-C101-066"]}]},{"name":"Foundation for Medical Research of the Tri-Service General Hospital","award":["TSGH-C102-063"],"award-info":[{"award-number":["TSGH-C102-063"]}]},{"name":"National Defense Medical Center","award":["DOD-100-I-27"],"award-info":[{"award-number":["DOD-100-I-27"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Liver International"],"published-print":{"date-parts":[[2015,8]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background &amp; Aims<\/jats:title>\n                    <jats:p>\n                      Gilbert's syndrome causes pharmacological variation in drug glucuronidation and unexpected toxicity from therapeutic agents. The two common genotypes of Gilbert's syndrome are a dinucleotide polymorphism (\n                      <jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content>\n                      )\n                      <jats:sub>7<\/jats:sub>\n                      in\n                      <jats:styled-content style=\"fixed-case\">TATA<\/jats:styled-content>\n                      \u2010Box as well as the 211G&gt;A mutation in the coding exon 1, particularly in Asians, of human\n                      <jats:italic>\n                        <jats:styled-content style=\"fixed-case\">UGT<\/jats:styled-content>\n                        1A1\n                      <\/jats:italic>\n                      gene. In this study, we aimed to establish an effective method to detect the 211G&gt;A mutation.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      The coding exon 1 sequence of human\n                      <jats:italic>\n                        <jats:styled-content style=\"fixed-case\">UGT<\/jats:styled-content>\n                        1A1\n                      <\/jats:italic>\n                      gene was analysed by Vector\n                      <jats:styled-content style=\"fixed-case\">NTI<\/jats:styled-content>\n                      software. The 211G&gt;A mutation in the coding exon\u00a01 of\n                      <jats:italic>\n                        <jats:styled-content style=\"fixed-case\">UGT<\/jats:styled-content>\n                        1A1\n                      <\/jats:italic>\n                      gene was determined by restriction fragment length polymorphism (\n                      <jats:styled-content style=\"fixed-case\">RFLP<\/jats:styled-content>\n                      ) method. Serum total bilirubin level was measured as well.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      A newly identified Bsm\n                      <jats:styled-content style=\"fixed-case\">BI<\/jats:styled-content>\n                      site was located in the coding exon 1 of\n                      <jats:italic>\n                        <jats:styled-content style=\"fixed-case\">UGT<\/jats:styled-content>\n                        1A1\n                      <\/jats:italic>\n                      gene. The 211G&gt;A mutation in the coding exon 1 of\n                      <jats:italic>\n                        <jats:styled-content style=\"fixed-case\">UGT<\/jats:styled-content>\n                        1A1\n                      <\/jats:italic>\n                      gene was determined by\n                      <jats:styled-content style=\"fixed-case\">DNA RFLP<\/jats:styled-content>\n                      . Furthermore, we reported our present work on genetic analysis of mutations of\n                      <jats:italic>\n                        <jats:styled-content style=\"fixed-case\">UGT<\/jats:styled-content>\n                        1A1\n                      <\/jats:italic>\n                      gene, and the correlation of\n                      <jats:italic>\n                        <jats:styled-content style=\"fixed-case\">UGT<\/jats:styled-content>\n                        1A1\n                      <\/jats:italic>\n                      mutations with serum total bilirubin levels in Taiwanese population. The results showed that 15 subjects carried 211G&gt;A mutation in 23 subjects related with Gilbert's syndrome. The homozygous 211G&gt;A mutant as well as simultaneously heterozygous mutants both in\n                      <jats:styled-content style=\"fixed-case\">TATA<\/jats:styled-content>\n                      \u2010Box and 211G&gt;A significantly increased the risk of Gilbert's syndrome similar to subjects carrying homozygous\n                      <jats:styled-content style=\"fixed-case\">TATA<\/jats:styled-content>\n                      \u2010Box mutant.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      Bsm\n                      <jats:styled-content style=\"fixed-case\">BI RFLP<\/jats:styled-content>\n                      is an effective method to detect 211G&gt;A mutation in the coding exon 1 of\n                      <jats:italic>\n                        <jats:styled-content style=\"fixed-case\">UGT<\/jats:styled-content>\n                        1A1\n                      <\/jats:italic>\n                      gene. The common 211G&gt;A mutation is one of the causes of Gilbert's syndrome in Taiwanese population.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/liv.12785","type":"journal-article","created":{"date-parts":[[2015,1,22]],"date-time":"2015-01-22T08:24:14Z","timestamp":1421915054000},"page":"2050-2056","source":"Crossref","is-referenced-by-count":10,"title":["Restriction fragment length polymorphism effectively identifies exon 1 mutation of\n                    <scp>UGT<\/scp>\n                    1A1 gene in patients with Gilbert's Syndrome"],"prefix":"10.1111","volume":"35","author":[{"given":"Tzu\u2010Yue","family":"Shiu","sequence":"first","affiliation":[{"name":"Division of Gastroenterology Department of Internal Medicine Tri\u2010Service General Hospital National Defense Medical Center Taipei 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