Long-Read Sequencing Unlocks Rare Genetic Cause of Inherited Ataxia
Researchers used long-read genome sequencing and RNA analysis to diagnose a rare hereditary ataxia caused by biallelic VPS41 variants, expanding ...
Researchers used long-read genome sequencing and RNA analysis to diagnose a rare hereditary ataxia caused by biallelic VPS41 variants, expanding ...
Researchers have identified TM184C as a GPCR-like protein that regulates both intercellular material exchange and autophagy, linking two fundamental membrane-based ...
Researchers have discovered that the autophagy protein AMBRA1 directly binds and allosterically opens the autoinhibited NLRP3 inflammasome, revealing a new ...
Recent research from the Tata Institute of Fundamental Research in Mumbai, India has shed light on an essential cellular process ...
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© 2025 Scienmag - Science Magazine