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J Collinge

Showing results (141-150 of 171) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|February 20, 2007
Familial prion disease in a Hungarian family with a novel 144-base pair insertion in the prion protein geneT Kovács, J A Beck, M I Papp, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1994
Familial Pick's disease and dementia in frontal lobe degeneration of non-Alzheimer type are not variants of prion diseaseJ Collinge, M S Palmer, K C Sidle, et al.
Neurology|January 29, 2003
Early onset familial Alzheimer's disease: Mutation frequency in 31 familiesJ C Janssen, J A Beck, T A Campbell, et al.
Archives of Neurology|May 1, 1997
Clinical characteristics of a chromosome 17-linked rapidly progressive familial frontotemporal dementiaH Basun, O Almkvist, K Axelman, et al.
Lancet (London, England)|January 7, 1989
Insertion in prion protein gene in familial Creutzfeldt-Jakob diseaseF Owen, M Poulter, R Lofthouse, et al.
Human Mutation|March 25, 1999
Pathogenic presenilin 1 mutations (P436S & I143F) in early-onset Alzheimer's disease in the UK. Mutations in brief no. 223. OnlineM S Palmer, J A Beck, T A Campbell, et al.
Nature|December 21, 1995
Unaltered susceptibility to BSE in transgenic mice expressing human prion proteinJ Collinge, M S Palmer, K C Sidle, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 11, 1994
Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion proteinG C Telling, M Scott, K K Hsiao, et al.
Science (New York, N.Y.)|March 19, 1999
Reversible conversion of monomeric human prion protein between native and fibrilogenic conformationsG S Jackson, L L Hosszu, A Power, et al.
Brain : a Journal of Neurology|March 2, 1999
Fatal familial insomnia: a new Austrian familyG Almer, J A Hainfellner, T Brücke, et al.
Pageof 18

Showing results (141-150 of 171) with videos related to

Sort By:
Pageof 18
Journal of Neurology, Neurosurgery, and Psychiatry|February 20, 2007
Familial prion disease in a Hungarian family with a novel 144-base pair insertion in the prion protein geneT Kovács, J A Beck, M I Papp, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1994
Familial Pick's disease and dementia in frontal lobe degeneration of non-Alzheimer type are not variants of prion diseaseJ Collinge, M S Palmer, K C Sidle, et al.
Neurology|January 29, 2003
Early onset familial Alzheimer's disease: Mutation frequency in 31 familiesJ C Janssen, J A Beck, T A Campbell, et al.
Archives of Neurology|May 1, 1997
Clinical characteristics of a chromosome 17-linked rapidly progressive familial frontotemporal dementiaH Basun, O Almkvist, K Axelman, et al.
Lancet (London, England)|January 7, 1989
Insertion in prion protein gene in familial Creutzfeldt-Jakob diseaseF Owen, M Poulter, R Lofthouse, et al.
Human Mutation|March 25, 1999
Pathogenic presenilin 1 mutations (P436S & I143F) in early-onset Alzheimer's disease in the UK. Mutations in brief no. 223. OnlineM S Palmer, J A Beck, T A Campbell, et al.
Nature|December 21, 1995
Unaltered susceptibility to BSE in transgenic mice expressing human prion proteinJ Collinge, M S Palmer, K C Sidle, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 11, 1994
Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion proteinG C Telling, M Scott, K K Hsiao, et al.
Science (New York, N.Y.)|March 19, 1999
Reversible conversion of monomeric human prion protein between native and fibrilogenic conformationsG S Jackson, L L Hosszu, A Power, et al.
Brain : a Journal of Neurology|March 2, 1999
Fatal familial insomnia: a new Austrian familyG Almer, J A Hainfellner, T Brücke, et al.
Pageof 18