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          <dc:title>Association of the C825T polymorphism of the G-protein β3 subunit gene with hypertension, obesity, hyperlipidemia, insulin resistance, diabetes, diabetic complications, and diabetic therapies among Japanese</dc:title>
          <jpcoar:creator>
            <jpcoar:creatorName>Hayakawa, Tetsuo</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:nameIdentifier nameIdentifierURI="https://kaken.nii.ac.jp/ja/search/?qm=00324111" nameIdentifierScheme="e-Rad">00324111</jpcoar:nameIdentifier>
            <jpcoar:creatorName>Takamura, Toshinari</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName>Abe, Toshio</jpcoar:creatorName>
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          <jpcoar:creator>
            <jpcoar:nameIdentifier nameIdentifierURI="https://kaken.nii.ac.jp/ja/search/?qm=60185923" nameIdentifierScheme="e-Rad">60185923</jpcoar:nameIdentifier>
            <jpcoar:creatorName>Kaneko, Shuichi</jpcoar:creatorName>
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          <datacite:description descriptionType="Abstract">A C825T polymorphism of the gene encoding the G-protein β3 subunit (GNB3) is associated with increased intracellular signal transduction. We know that this C825T polymorphism may influence hypertension and obesity. In whites, the C825T polymorphism has been reported to induce hypertension, obesity, and diabetic nephropathy. Thus, we investigated how genetic variation in the GNB3 gene is associated with hypertension, obesity, insulin resistance, diabetes, diabetic complications, and diabetic therapies in 427 Japanese subjects with type 2 diabetes mellitus and in 368 Japanese subjects who underwent general health examinations. The frequency of the GNB3 gene polymorphism was 0.48 and 0.47 in subjects with diabetes and in those who had general health examinations, respectively. The amount of hyperlipidemia of the CT allele was significantly lower than the amount in the CC allele in the Japanese subjects with diabetes. Our results suggest that the C825T polymorphism influences lipid metabolism and is not associated with hypertension, obesity, insulin resistance, diabetes, diabetic complications, or diabetic therapies. © 2007.</datacite:description>
          <datacite:description descriptionType="Other">金沢大学大学院医学系研究科環境社会医学</datacite:description>
          <dc:publisher>Elsevier BV</dc:publisher>
          <datacite:date dateType="Issued">2007-01-01</datacite:date>
          <datacite:date>2017-10-03</datacite:date>
          <dc:language>eng</dc:language>
          <dc:type rdf:resource="http://purl.org/coar/resource_type/c_6501">journal article</dc:type>
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          <jpcoar:identifier identifierType="HDL">http://hdl.handle.net/2297/3469</jpcoar:identifier>
          <jpcoar:identifier identifierType="URI">https://kanazawa-u.repo.nii.ac.jp/records/13200</jpcoar:identifier>
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            <jpcoar:relatedIdentifier identifierType="DOI">https://doi.org/10.1016/j.metabol.2006.08.020</jpcoar:relatedIdentifier>
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            <jpcoar:relatedIdentifier identifierType="URI">http://www.elsevier.com/locate/issn/00260495</jpcoar:relatedIdentifier>
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          <jpcoar:sourceIdentifier identifierType="NCID">AA0073583X</jpcoar:sourceIdentifier>
          <jpcoar:sourceIdentifier identifierType="ISSN">0026-0495</jpcoar:sourceIdentifier>
          <jpcoar:sourceTitle>Metabolism: Clinical and Experimental</jpcoar:sourceTitle>
          <jpcoar:volume>56</jpcoar:volume>
          <jpcoar:issue>1</jpcoar:issue>
          <jpcoar:pageStart>44</jpcoar:pageStart>
          <jpcoar:pageEnd>48</jpcoar:pageEnd>
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            <datacite:date dateType="Available">2017-10-03</datacite:date>
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