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applebyb's Joiner [4 articles]

Recent papers posted to applebyb's library by the author Joiner. You can also see everyone's Joiner.
  • Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series.
    Brain : a journal of neurology (1 September 2008)
    by T E F E Webb, M Poulter, J Beck, J Uphill, G Adamson, T Campbell, J Linehan, C Powell, S Brandner, S Pal, D Siddique, J D D Wadsworth, S Joiner, K Alner, C Petersen, S Hampson, C Rhymes, C Treacy, E Storey, M D D Geschwind, A H H Nemeth, S Wroe, J Collinge, S Mead
    posted to prion phenotype p102l gss by applebyb on 2008-09-06 19:32:41 as ****
  • First Report of Creutzfeldt-Jakob Disease Occurring in 2 Siblings Unexplained by PRNP Mutation.
    Journal of neuropathology and experimental neurology (19 August 2008)
    by Thomas E Webb, Suvankar Pal, Durrenajaf Siddique, Dominic C Heaney, Jacqueline M Linehan, Jonathan D Wadsworth, Susan Joiner, Jon Beck, Stephen J Wroe, Valerie Stevenson, Sebastian Brandner, Simon Mead, John Collinge
    posted to fcjd prnp scjd by applebyb on 2008-08-26 02:14:43 as ****
  • Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice
    Proceedings of the National Academy of Sciences, Vol. 105, No. 10. (11 March 2008), pp. 3885-3890.
    by Jonathan D Wadsworth, Susan Joiner, Jacqueline M Linehan, Melanie Desbruslais, Katie Fox, Sharon Cooper, Sabrina Cronier, Emmanuel A Asante, Simon Mead, Sebastian Brandner, Andrew F Hill, John Collinge
    posted to cre kuru scjd by applebyb on 2008-03-12 00:47:51 as **
  • Human prion protein with valine 129 prevents expression of variant CJD phenotype.
    Science, Vol. 306, No. 5702. (3 December 2004), pp. 1793-1796.
    by JD Wadsworth, EA Asante, M Desbruslais, JM Linehan, S Joiner, I Gowland, J Welch, L Stone, SE Lloyd, AF Hill, S Brandner, J Collinge
    posted to prpsc vcjd by applebyb on 2008-02-12 00:39:17 as read
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