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Nature 405, 415 (25 May 2000) | doi:10.1038/35013197
Open Innovation Challenges
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Direct Molecular Detection of Proteins and Nucleic Acids
This Challenge is looking for novel approaches to protein and nucleic acid detection. This is an Id...
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Single-cell Analysis Platform
This Challenge is looking for novel approaches to analyzing changes at a single-cell level. This is...
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- The University of Texas Southwestern Medical Center
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DNA repair: The bases for Cockayne syndrome
Philip C. Hanawalt
Cockayne syndrome is a rare human hereditary disease, characterized by growth failure, deficient neurological development and severe sensitivity to sunlight. It can arise from mutations in any one of five genes.
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