Kenjiro Kosaki 研究室
主宰者：Kenjiro Kosaki
慶應義塾大学
AI 要約（直近 5 年の研究成果）
Kenjiro Kosaki研究室は、遺伝子の異常が原因となる様々な疾患の診断と治療法開発に取り組んでいます。特に、患者のDNA配列を調べるゲノム解析技術を用いて、これまで原因不明だった病気の遺伝的背景を明らかにすることに力を入れています。小頭症や発達障害、けいれん性脳症、難聴、眼病など、多くの神経発達に関わる疾患を対象としており、各疾患でどの遺伝子がどのように異常になると病気が起こるのかを詳しく調べています。
さらに、単に原因遺伝子を特定するだけでなく、実験室での細胞実験やマウスを使った動物実験を通じて、その遺伝子異常がどのようなメカニズムで病気につながるのかを解明しています。例えば、乳がんのリスク遺伝子や脳の発達に重要な遺伝子など、様々な遺伝子について、変異がどのように機能障害を引き起こすのかを機能解析により明らかにしています。これらの研究成果は、患者さんの正確な診断につながるだけでなく、新しい治療法の開発や個人に合わせた医療の実現に貢献することを目指しています。
※ AI（Claude）が、公開されている論文要旨から研究の問い・手法・主要な発見を事実情報として抽出・再構成して自動生成しています。誤りを含む可能性があるため、正確性は研究室公式情報でご確認ください。
外部リンク
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科研費（0 件）
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所属学会・役職（0 件）
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