Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series

By Webb T. E. F.  

Brain, Vol. 131, Iss. 10, 2008-10 ,pp. : 2632-2646

Oxford University Press

Access to resources Recommend Favorite

Spongiform encephalopathy in siblings with no evidence of protease-resistant prion protein or a mutation in the prion protein gene

By Varges Daniela   Schulz-Schaeffer Walter   Wemheuer Wiebke   Damman Insa   Schmitz Matthias   Cramm Maria   Kallenberg Kai   Shirneshan Katayoon   Elkenani Manar   Markwort Susanne   Faist Michael   Kohlhase Jürgen   Windl Otto   Zerr Inga  

Journal of Neurology, Vol. 260, Iss. 7, 2013-07 ,pp. : 1871-1879

Springer Publishing Company

Access to resources Recommend Favorite

Inherited prion disease with six octapeptide repeat insertional mutation—molecular analysis of phenotypic heterogeneity

By Mead Simon   Poulter Mark   Beck Jon   Webb Thomas E. F.   Campbell Tracy A.   Linehan Jacqueline M.   Desbruslais Melanie   Joiner Susan   Wadsworth Jonathan D. F.   King Andrew   Lantos Peter   Collinge John  

Brain, Vol. 129, Iss. 9, 2006-09 ,pp. : 2297-2317

Oxford University Press

Access to resources Recommend Favorite

Distinct glycoform ratios of protease resistant prion protein associated with PRNP point mutations

By Hill Andrew F.   Joiner Susan   Beck Jonathan A.   Campbell Tracy A.   Dickinson Andrew   Poulter Mark   Wadsworth Jonathan D. F.   Collinge John  

Brain, Vol. 129, Iss. 3, 2006-03 ,pp. : 676-685

Oxford University Press

Access to resources Recommend Favorite

Mutant Prion Protein D202N Associated with Familial Prion Disease is Retained in the Endoplasmic Reticulum and Forms ‘Curly’ Intracellular Aggregates

By Gu Yaping   Verghese Susamma   Bose Sharmila   Mohan Maradumane   Singh Neena  

Journal of Molecular Neuroscience, Vol. 32, Iss. 1, 2007-05 ,pp. : 90-96

Humana Press, Inc

Access to resources Recommend Favorite