In Rare Disease, a Familiar Protein Disrupts Gene Function
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In Rare Disease, a Familiar Protein Disrupts Gene Function
An international team of scientists studying a rare genetic disease discovered that a bundle of proteins with the long-established function of keeping chromosomes together also plays an important role in regulating genes in humans. The finding that cohesin, a protein complex, dysregulates gene expression may improve diagnosis of the multisystem genetic disease Cornelia de Lange syndrome.
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Tags: Genetic, Disease and Condition, Protein, Genes, Scientist
Most Recently Shared on May 27, 2009 at 12:52 am By:
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