David Corey, PhD
Bertarelli Professor of Translational Medical Science, Harvard Medical School
The genomic structure of the gene defective in Usher syndrome type Ib (MYO7A).
Authors: Authors: Kelley PM, Weston MD, Chen ZY, Orten DJ, Hasson T, Overbeck LD, Pinnt J, Talmadge CB, Ing P, Mooseker MS, Corey D, Sumegi J, Kimberling WJ.
Genomics
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Genomics
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Loss of Na+ channel inactivation by anemone toxin (ATX II) mimics the myotonic state in hyperkalaemic periodic paralysis.
Glial and neuronal forms of the voltage-dependent sodium channel: characteristics and cell-type distribution.
Are TMCs the Mechanotransduction Channels of Vertebrate Hair Cells?
Sorting out a promiscuous superfamily: towards cadherin connectomics.
Stringing the fiddle: the inner ear's two-part invention.
A gradient of single-channel conductance in the cochlea: tuning the cochlea's strings?
Myosin-X, a novel myosin with pleckstrin homology domains, associates with regions of dynamic actin.
Authors: Authors: Berg JS, Derfler BH, Pennisi CM, Corey DP, Cheney RE.
J Cell Sci
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J Cell Sci
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The molecules of mechanosensation.
Theoretical reconstruction of myotonia and paralysis caused by incomplete inactivation of sodium channels.