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  • 執筆者の写真hkytara
    • 2021年6月14日

A new paper has been published.

更新日：2021年8月2日

木村助教のドイツでの仕事で、ヒトの難治性筋原線維性ミオパチーの原因遺伝子であるBAG3遺伝子変異をマウスで再現させて病態を解明した論文が発表されました。

Congrats Ken! His paper investigating the underlying mechanism of childhood cardiomyopathy caused by the mutation in the BAG3 gene has been published.


論文はこちら

Link to the paper→ https://www.nature.com/articles/s41467-021-23858-7

筑波大学のリサーチニュースはこちら→https://www.tsukuba.ac.jp/journal/medicine-health/20210611180000.html?fbclid=IwAR0cWtDO6VZIJ3JMp-l6RG7Xg5Q8HQeIaXZd81_J8VJohb6_ddNaoNVh9hA

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