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J Collinge

Showing results (121-130 of 171) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|May 17, 2001
Identification of multiple quantitative trait loci linked to prion disease incubation period in miceS E Lloyd, O N Onwuazor, J A Beck, 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.
Neurology|February 24, 2010
Brain-water diffusion coefficients reflect the severity of inherited prion diseaseH Hyare, S Wroe, D Siddique, et al.
Journal of Molecular Biology|August 9, 2001
XAFS study of the high-affinity copper-binding site of human PrP(91-231) and its low-resolution structure in solutionS S Hasnain, L M Murphy, R W Strange, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 22, 1998
Chromosome 14 familial Alzheimer's disease: the clinical and neuropathological characteristics of a family with a leucine-->serine (L250S) substitution at codon 250 of the presenilin 1 geneR J Harvey, D Ellison, J Hardy, et al.
Gut|June 10, 2006
Prion infectivity in variant Creutzfeldt-Jakob disease rectumJ D F Wadsworth, S Joiner, K Fox, 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|October 30, 2009
Corticobasal syndrome associated with a novel 1048_1049insG progranulin mutationJ D Rohrer, J Beck, J D Warren, et al.
Journal of the Neurological Sciences|February 1, 1993
Genetic characterization of a familial non-specific dementia originating in Jutland, DenmarkJ Brown, S Gydesen, S A Sorensen, et al.
Pageof 18

Showing results (121-130 of 171) with videos related to

Sort By:
Pageof 18
Proceedings of the National Academy of Sciences of the United States of America|May 17, 2001
Identification of multiple quantitative trait loci linked to prion disease incubation period in miceS E Lloyd, O N Onwuazor, J A Beck, 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.
Neurology|February 24, 2010
Brain-water diffusion coefficients reflect the severity of inherited prion diseaseH Hyare, S Wroe, D Siddique, et al.
Journal of Molecular Biology|August 9, 2001
XAFS study of the high-affinity copper-binding site of human PrP(91-231) and its low-resolution structure in solutionS S Hasnain, L M Murphy, R W Strange, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 22, 1998
Chromosome 14 familial Alzheimer's disease: the clinical and neuropathological characteristics of a family with a leucine-->serine (L250S) substitution at codon 250 of the presenilin 1 geneR J Harvey, D Ellison, J Hardy, et al.
Gut|June 10, 2006
Prion infectivity in variant Creutzfeldt-Jakob disease rectumJ D F Wadsworth, S Joiner, K Fox, 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|October 30, 2009
Corticobasal syndrome associated with a novel 1048_1049insG progranulin mutationJ D Rohrer, J Beck, J D Warren, et al.
Journal of the Neurological Sciences|February 1, 1993
Genetic characterization of a familial non-specific dementia originating in Jutland, DenmarkJ Brown, S Gydesen, S A Sorensen, et al.
Pageof 18