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Matthew T Bishop

Showing results (11-20 of 22) with videos related to

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Plos One|August 7, 2008
No major change in vCJD agent strain after secondary transmission via blood transfusionMatthew T Bishop, Diane L Ritchie, Robert G Will, et al.
Lancet (London, England)|February 14, 2003
MHC typing in variant Creutzfeldt-Jakob diseaseMark B Pepys, Alison Bybee, David R Booth, et al.
BMC Medical Genetics|December 13, 2007
No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob diseasePascual Sánchez-Juan, Matthew T Bishop, Alison Green, et al.
ACS Combinatorial Science|June 4, 2016
A Novel High-Throughput ViscometerSuraj Deshmukh, Matthew T Bishop, Daniel Dermody, et al.
BMJ (Clinical Research Ed.)|April 12, 2006
Variant Creutzfeldt-Jakob disease: prion protein genotype analysis of positive appendix tissue samples from a retrospective prevalence studyJames W Ironside, Matthew T Bishop, Kelly Connolly, et al.
Transfusion|November 5, 2008
Human platelets as a substrate source for the in vitro amplification of the abnormal prion protein (PrP) associated with variant Creutzfeldt-Jakob diseaseMichael Jones, Alexander H Peden, Helen Yull, et al.
Annals of Neurology|June 3, 2004
Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: UK cases 1991-2002Mark W Head, Tristan J R Bunn, Matthew T Bishop, et al.
Brain : a Journal of Neurology|May 28, 2011
Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factorsDiego N Kaski, Catherine Pennington, Jon Beck, et al.
Brain Pathology (Zurich, Switzerland)|February 1, 2012
MM2-thalamic Creutzfeldt-Jakob disease: neuropathological, biochemical and transmission studies identify a distinctive prion strainFabio Moda, Silvia Suardi, Giuseppe Di Fede, et al.
Plos One|May 5, 2012
Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspectsCasper Jansen, Piero Parchi, Sabina Capellari, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Plos One|August 7, 2008
No major change in vCJD agent strain after secondary transmission via blood transfusionMatthew T Bishop, Diane L Ritchie, Robert G Will, et al.
Lancet (London, England)|February 14, 2003
MHC typing in variant Creutzfeldt-Jakob diseaseMark B Pepys, Alison Bybee, David R Booth, et al.
BMC Medical Genetics|December 13, 2007
No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob diseasePascual Sánchez-Juan, Matthew T Bishop, Alison Green, et al.
ACS Combinatorial Science|June 4, 2016
A Novel High-Throughput ViscometerSuraj Deshmukh, Matthew T Bishop, Daniel Dermody, et al.
BMJ (Clinical Research Ed.)|April 12, 2006
Variant Creutzfeldt-Jakob disease: prion protein genotype analysis of positive appendix tissue samples from a retrospective prevalence studyJames W Ironside, Matthew T Bishop, Kelly Connolly, et al.
Transfusion|November 5, 2008
Human platelets as a substrate source for the in vitro amplification of the abnormal prion protein (PrP) associated with variant Creutzfeldt-Jakob diseaseMichael Jones, Alexander H Peden, Helen Yull, et al.
Annals of Neurology|June 3, 2004
Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: UK cases 1991-2002Mark W Head, Tristan J R Bunn, Matthew T Bishop, et al.
Brain : a Journal of Neurology|May 28, 2011
Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factorsDiego N Kaski, Catherine Pennington, Jon Beck, et al.
Brain Pathology (Zurich, Switzerland)|February 1, 2012
MM2-thalamic Creutzfeldt-Jakob disease: neuropathological, biochemical and transmission studies identify a distinctive prion strainFabio Moda, Silvia Suardi, Giuseppe Di Fede, et al.
Plos One|May 5, 2012
Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspectsCasper Jansen, Piero Parchi, Sabina Capellari, et al.
Pageof 3