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K C Sidle

Showing results (1-10 of 13) with videos related to

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Nature|October 24, 1996
Molecular analysis of prion strain variation and the aetiology of 'new variant' CJDJ Collinge, K C Sidle, J Meads, et al.
Multiple Sclerosis and Related Disorders|April 17, 2015
Myasthenia gravis and neuromyelitis opica: A causal linkJ Spillane, G Christofi, K C Sidle, et al.
BMJ (Clinical Research Ed.)|January 30, 1993
Inherited prion disease (PrP lysine 200) in Britain: two case reportsJ Collinge, M S Palmer, T Campbell, et al.
Lancet (London, England)|August 26, 1995
Transmission of fatal familial insomnia to laboratory animalsJ Collinge, M S Palmer, K C Sidle, et al.
Neuroscience Letters|December 1, 1998
Molecular screening of sheep for bovine spongiform encephalopathyA F Hill, K C Sidle, S Joiner, et al.
Nature|October 23, 1997
The same prion strain causes vCJD and BSEA F Hill, M Desbruslais, S Joiner, et al.
Nature|July 28, 1994
Prion protein is necessary for normal synaptic functionJ Collinge, M A Whittington, K C Sidle, et al.
Human Molecular Genetics|May 1, 1993
Deletions in the prion protein gene are not associated with CJDM S Palmer, S P Mahal, T A Campbell, et al.
Nature Genetics|February 1, 1995
Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion proteinM A Whittington, K C Sidle, I Gowland, 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.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Nature|October 24, 1996
Molecular analysis of prion strain variation and the aetiology of 'new variant' CJDJ Collinge, K C Sidle, J Meads, et al.
Multiple Sclerosis and Related Disorders|April 17, 2015
Myasthenia gravis and neuromyelitis opica: A causal linkJ Spillane, G Christofi, K C Sidle, et al.
BMJ (Clinical Research Ed.)|January 30, 1993
Inherited prion disease (PrP lysine 200) in Britain: two case reportsJ Collinge, M S Palmer, T Campbell, et al.
Lancet (London, England)|August 26, 1995
Transmission of fatal familial insomnia to laboratory animalsJ Collinge, M S Palmer, K C Sidle, et al.
Neuroscience Letters|December 1, 1998
Molecular screening of sheep for bovine spongiform encephalopathyA F Hill, K C Sidle, S Joiner, et al.
Nature|October 23, 1997
The same prion strain causes vCJD and BSEA F Hill, M Desbruslais, S Joiner, et al.
Nature|July 28, 1994
Prion protein is necessary for normal synaptic functionJ Collinge, M A Whittington, K C Sidle, et al.
Human Molecular Genetics|May 1, 1993
Deletions in the prion protein gene are not associated with CJDM S Palmer, S P Mahal, T A Campbell, et al.
Nature Genetics|February 1, 1995
Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion proteinM A Whittington, K C Sidle, I Gowland, 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.
Pageof 2