Area of research
Molecular Biology · Neurology
Research interest
Research focused on Glycosylation and PRNP, with related work in Residue (chemistry), Phenotype, In vitro. Notable publications include 'Co-existence of PrPD types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics', 'Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases', and 'Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone'.
Generation of human chronic wasting disease in transgenic mice
Co-existence of PrPD types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics
Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone
Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases
Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease
Correction: Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease