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, sizes, and densities, including variants targeting multiple immune lectins. • Characterize lectin–glycodomain interactions using NMR, MS, and ITC to determine binding specificity, affinity, and
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(DSBs) in the F1 generation, where a highly enriched heterochromatin structure blocks the accessibility of homologous recombination (HR) repair machinery. This project will investigate how DNA damage in
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of invariants of operator algebras, such as K-theory and cyclic homology; and Developing a mathematical method for passing from numerical Berry curvature to robust topological invariants in a large class of cases
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highly enriched heterochromatin structure blocks the accessibility of homologous recombination (HR) repair machinery. This project will investigate how DNA damage in sperm alters the epigenome