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J Collinge

Showing results (131-140 of 171) with videos related to

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Nature Structural Biology|July 30, 1999
Structural mobility of the human prion protein probed by backbone hydrogen exchangeL L Hosszu, N J Baxter, G S Jackson, et al.
Brain Pathology (Zurich, Switzerland)|July 1, 1995
Tissue handling in suspected Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases)H Budka, A Aguzzi, P Brown, et al.
Brain : a Journal of Neurology|June 1, 1992
Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological featuresJ Collinge, J Brown, J Hardy, et al.
The British Journal of Psychiatry : the Journal of Mental Science|May 1, 1991
Evidence for a pseudo-autosomal locus for schizophrenia using the method of affected sibling pairsJ Collinge, L E Delisi, A Boccio, et al.
Neurology|July 27, 2001
Two-octapeptide repeat deletion of prion protein associated with rapidly progressive dementiaJ A Beck, S Mead, T A Campbell, et al.
Brain : a Journal of Neurology|June 1, 1992
Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studiesM Poulter, H F Baker, C D Frith, et al.
Experimental Neurology|May 1, 1991
Insertions in the prion protein gene in atypical dementiasF Owen, M Poulter, J Collinge, et al.
Translational Psychiatry|April 22, 2015
Genome-wide association study of behavioural and psychiatric features in human prion diseaseA G B Thompson, J Uphill, J Lowe, et al.
Nature Communications|April 21, 2011
Rapid cell-surface prion protein conversion revealed using a novel cell systemR Goold, S Rabbanian, L Sutton, et al.
Lancet (London, England)|July 7, 1990
Prion dementia without characteristic pathologyJ Collinge, F Owen, M Poulter, et al.
Pageof 18

Showing results (131-140 of 171) with videos related to

Sort By:
Pageof 18
Nature Structural Biology|July 30, 1999
Structural mobility of the human prion protein probed by backbone hydrogen exchangeL L Hosszu, N J Baxter, G S Jackson, et al.
Brain Pathology (Zurich, Switzerland)|July 1, 1995
Tissue handling in suspected Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases)H Budka, A Aguzzi, P Brown, et al.
Brain : a Journal of Neurology|June 1, 1992
Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological featuresJ Collinge, J Brown, J Hardy, et al.
The British Journal of Psychiatry : the Journal of Mental Science|May 1, 1991
Evidence for a pseudo-autosomal locus for schizophrenia using the method of affected sibling pairsJ Collinge, L E Delisi, A Boccio, et al.
Neurology|July 27, 2001
Two-octapeptide repeat deletion of prion protein associated with rapidly progressive dementiaJ A Beck, S Mead, T A Campbell, et al.
Brain : a Journal of Neurology|June 1, 1992
Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studiesM Poulter, H F Baker, C D Frith, et al.
Experimental Neurology|May 1, 1991
Insertions in the prion protein gene in atypical dementiasF Owen, M Poulter, J Collinge, et al.
Translational Psychiatry|April 22, 2015
Genome-wide association study of behavioural and psychiatric features in human prion diseaseA G B Thompson, J Uphill, J Lowe, et al.
Nature Communications|April 21, 2011
Rapid cell-surface prion protein conversion revealed using a novel cell systemR Goold, S Rabbanian, L Sutton, et al.
Lancet (London, England)|July 7, 1990
Prion dementia without characteristic pathologyJ Collinge, F Owen, M Poulter, et al.
Pageof 18