Showing results (1-10 of 21) with videos related to
Sort By:
Pageof 3
Human Mutation|June 14, 2008
Successful amplification of degraded DNA for use with high-throughput SNP genotyping platformsSimon Mead, Mark Poulter, John Beck, et al.Brain : a Journal of Neurology|January 18, 2006
Distinct glycoform ratios of protease resistant prion protein associated with PRNP point mutationsAndrew F Hill, Susan Joiner, Jonathan A Beck, et al.Human Molecular Genetics|May 17, 2014
In vitro screen of prion disease susceptibility genes using the scrapie cell assayCraig A Brown, Christian Schmidt, Mark Poulter, et al.Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|October 14, 2008
Genetic susceptibility, evolution and the kuru epidemicSimon Mead, Jerome Whitfield, Mark Poulter, et al.Neurobiology of Aging|January 4, 2011
Duplication of amyloid precursor protein (APP), but not prion protein (PRNP) gene is a significant cause of early onset dementia in a large UK seriesDaniel McNaughton, William Knight, Rita Guerreiro, et al.Human Mutation|June 29, 2010
PRNP allelic series from 19 years of prion protein gene sequencing at the MRC Prion UnitJon A Beck, Mark Poulter, Tracy A Campbell, et al.Science (New York, N.Y.)|April 12, 2003
Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemicsSimon Mead, Michael P H Stumpf, Jerome Whitfield, et al.Human Molecular Genetics|April 30, 2004
Somatic and germline mosaicism in sporadic early-onset Alzheimer's diseaseJonathan A Beck, Mark Poulter, Tracy A Campbell, et al.Neurobiology of Aging|March 2, 2015
Rare structural genetic variation in human prion diseasesAna Lukic, James Uphill, Craig A Brown, et al.Brain : a Journal of Neurology|August 23, 2006
Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneitySimon Mead, Mark Poulter, Jon Beck, et al.Pageof 3