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        <identifier>oai:kumadai.repo.nii.ac.jp:00030235</identifier>
        <datestamp>2026-01-19T07:03:48Z</datestamp>
        <setSpec>343:347:348:349</setSpec>
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        <oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns="http://www.w3.org/2001/XMLSchema" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
          <dc:title>Novel intronic polymorphisms in the presenilin-2 gene and a case-control association study of Alzheimer's disease</dc:title>
          <dc:title>プレセニリン-2遺伝子における新たなイントロン多型とアルツハイマー病の患者-対象調査について</dc:title>
          <dc:title>プレセニリン 2 イデンシ ニ オケル アラタ ナ イントロン タケイ ト アルツハイマービョウ ノ カンジャ タイショウ チョウサ ニ ツイテ</dc:title>
          <dc:creator>本田, 雅博</dc:creator>
          <dc:creator>ホンダ, マサヒロ</dc:creator>
          <dc:creator>Honda, Masahiro</dc:creator>
          <dc:subject>377.5</dc:subject>
          <dc:subject>Alzheimer's disease</dc:subject>
          <dc:subject>presenilin-2 gene</dc:subject>
          <dc:subject>polymorphism</dc:subject>
          <dc:description>熊本大学</dc:description>
          <dc:description>博士（医学）</dc:description>
          <dc:description>Several alleles of introns or untranslated regions in the presenilin-1 (PS-1) and presenilin-2 (PS-2) genes have been reported to behave as risk factors for senile Alzheimer’s disease (AD). On the other hand, mutations in the three presenile AD genes also have been identified in a small number of sporadic presenile AD and senile AD cases. The present study evaluated the genetic contributions of PS-2 exons and introns to 56 senile and 18 Japanese cases of presenile AD using polymerase chain reaction single-strand conformation polymorphism analysis. In the PS-2 gene, one exonic polymorphic site without amino acid substitution, 9 intronic polymorphic sites, and 2 intronic variant sites were detected. However, in all cases, amino acid substitutions in exons between 4 and 12 of the PS-2 gene were not observed. The risk factors of senile and presenile AD were evaluated using a population-based study of restriction cleavages between patients and controls in introns 3, 4, 10 and 11. Regarding PS-2, there was no association between AD and intronic polymorphisms.</dc:description>
          <dc:description>http://onlinelibrary.wiley.com/doi/10.1046/j.1440-1819.1999.00609.x/full</dc:description>
          <dc:description>thesis</dc:description>
          <dc:publisher>熊本大学</dc:publisher>
          <dc:date>1999-03-25</dc:date>
          <dc:date>1999-03-25</dc:date>
          <dc:type>AM</dc:type>
          <dc:format>application/pdf</dc:format>
          <dc:identifier>Psychiatry and Clinical Neurosciences</dc:identifier>
          <dc:identifier>5</dc:identifier>
          <dc:identifier>53</dc:identifier>
          <dc:identifier>579</dc:identifier>
          <dc:identifier>585</dc:identifier>
          <dc:identifier>甲第1235号</dc:identifier>
          <dc:identifier>https://kumadai.repo.nii.ac.jp/record/30235/files/22_1235.pdf</dc:identifier>
          <dc:identifier>http://hdl.handle.net/2298/38301</dc:identifier>
          <dc:identifier>https://kumadai.repo.nii.ac.jp/records/30235</dc:identifier>
          <dc:language>eng</dc:language>
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