A new study has discovered a muscle disorder caused by mutations in a key protein.

Published Date: 05 Jun 2024

According to a recent study, the SMCHD1 protein directly influences the progression of facioscapulohumeral muscular dystrophy (FSHD) by regulating the way genes are processed. this finding about the role of SMCHD1.

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A new discovery from the lab of YouYang Zhao, Ph.D., from Stanley Manne Children's Research Institute at Ann & Robert H. Lurie Children's Hospital of Chicago, opens promising new directions for treatment of life-threatening ...

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In a major step forward for cancer care, researchers at ChristianaCare's Gene Editing Institute have shown that disabling the NRF2 gene with CRISPR technology can reverse chemotherapy resistance in lung cancer. The approach ...

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