Gene Therapy for Duchenne Muscular Dystrophy:
A Beacon of Hope in Genetic Medicine
Duchenne muscular dystrophy (DMD) is a devastating genetic disorder that has long evaded effective treatment. As the world of genetic medicine evolves, groundbreaking therapies like CRISPR... Read More
Targeted Protein Degradation: The Nuclear Option In Protein Druggability
Targeted Protein Degradation (TPD) is an innovative approach in drug development that aims to selectively remove specific proteins from cells to treat diseases. Traditional drug therapies often target proteins by blocking... Read More
CRISPR: A new Modality for Regenerative Medicine
Introduced in a 2013 paper by two biochemists, CRISPR, short for Clustered Regularly Interspaced Short Palindromic Repeats, is a gene-editing tool. This technology has reshaped global scientific landscapes and raised questions about the... Read More
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