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American Journal of Human Genetics
|
December 1, 1991
Presymptomatic detection or exclusion of prion protein gene defects in families with inherited prion diseases
J Collinge, M Poulter, M B Davis, et al.
Neurology
|
March 1, 1996
A prion disease with a novel 96-base pair insertional mutation in the prion protein gene
T A Campbell, M S Palmer, R G Will, et al.
Nature
|
November 20, 2001
HLA-DQ7 antigen and resistance to variant CJD
G S Jackson, J A Beck, C Navarrete, et al.
Lancet (London, England)
|
July 19, 1997
Is the neuropathology of new variant Creutzfeldt-Jakob disease and kuru similar?
P L Lantos, K Bhatia, L J Doey, et al.
Neuroscience Letters
|
December 1, 1998
Molecular screening of sheep for bovine spongiform encephalopathy
A F Hill, K C Sidle, S Joiner, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 5, 2001
Location and properties of metal-binding sites on the human prion protein
G S Jackson, I Murray, L L Hosszu, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 31, 2010
Familial Alzheimer's disease and inherited prion disease in the UK are poorly ascertained
J C Stevens, J Beck, A Lukic, et al.
Human Mutation
|
January 1, 1996
Sequence variation in intron of prion protein gene, crucial for complete diagnostic strategies
M S Palmer, R H van Leeven, S P Mahal, et al.
The EMBO Journal
|
February 2, 2002
Post-natal knockout of prion protein alters hippocampal CA1 properties, but does not result in neurodegeneration
G R Mallucci, S Ratté, E A Asante, et al.
AJNR. American Journal of Neuroradiology
|
December 17, 2009
High-b-value diffusion MR imaging and basal nuclei apparent diffusion coefficient measurements in variant and sporadic Creutzfeldt-Jakob disease
H Hyare, J Thornton, J Stevens, et al.
Page
of 18
Search research articles
Search
Showing results (101-110 of 171) with videos related to
Sort By:
Page
of 18
American Journal of Human Genetics
|
December 1, 1991
Presymptomatic detection or exclusion of prion protein gene defects in families with inherited prion diseases
J Collinge, M Poulter, M B Davis, et al.
Neurology
|
March 1, 1996
A prion disease with a novel 96-base pair insertional mutation in the prion protein gene
T A Campbell, M S Palmer, R G Will, et al.
Nature
|
November 20, 2001
HLA-DQ7 antigen and resistance to variant CJD
G S Jackson, J A Beck, C Navarrete, et al.
Lancet (London, England)
|
July 19, 1997
Is the neuropathology of new variant Creutzfeldt-Jakob disease and kuru similar?
P L Lantos, K Bhatia, L J Doey, et al.
Neuroscience Letters
|
December 1, 1998
Molecular screening of sheep for bovine spongiform encephalopathy
A F Hill, K C Sidle, S Joiner, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 5, 2001
Location and properties of metal-binding sites on the human prion protein
G S Jackson, I Murray, L L Hosszu, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 31, 2010
Familial Alzheimer's disease and inherited prion disease in the UK are poorly ascertained
J C Stevens, J Beck, A Lukic, et al.
Human Mutation
|
January 1, 1996
Sequence variation in intron of prion protein gene, crucial for complete diagnostic strategies
M S Palmer, R H van Leeven, S P Mahal, et al.
The EMBO Journal
|
February 2, 2002
Post-natal knockout of prion protein alters hippocampal CA1 properties, but does not result in neurodegeneration
G R Mallucci, S Ratté, E A Asante, et al.
AJNR. American Journal of Neuroradiology
|
December 17, 2009
High-b-value diffusion MR imaging and basal nuclei apparent diffusion coefficient measurements in variant and sporadic Creutzfeldt-Jakob disease
H Hyare, J Thornton, J Stevens, et al.
Page
of 18