R. Scott Hansen
Department of Medicine
University of Washington
Seattle
WA 98195
USA
Name/email consistency: low
- X inactivation-specific methylation of LINE-1 elements by DNMT3B: implications for the Lyon repeat hypothesis. Hansen, R.S. Hum. Mol. Genet. (2003)
- Escape from gene silencing in ICF syndrome: evidence for advanced replication time as a major determinant. Hansen, R.S., Stöger, R., Wijmenga, C., Stanek, A.M., Canfield, T.K., Luo, P., Matarazzo, M.R., D'Esposito, M., Feil, R., Gimelli, G., Weemaes, C.M., Laird, C.D., Gartler, S.M. Hum. Mol. Genet. (2000)
- The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome. Hansen, R.S., Wijmenga, C., Luo, P., Stanek, A.M., Canfield, T.K., Weemaes, C.M., Gartler, S.M. Proc. Natl. Acad. Sci. U.S.A. (1999)