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Mark W Head

Showing results (41-50 of 68) with videos related to

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Acta Neuropathologica Communications|October 22, 2014
The prion protein protease sensitivity, stability and seeding activity in variably protease sensitive prionopathy brain tissue suggests molecular overlaps with sporadic Creutzfeldt-Jakob diseaseAlexander H Peden, Deep P Sarode, Carl R Mulholland, et al.
Acta Neuropathologica|November 5, 2016
UK Iatrogenic Creutzfeldt-Jakob disease: investigating human prion transmission across genotypic barriers using human tissue-based and molecular approachesDiane L Ritchie, Marcelo A Barria, Alexander H Peden, et al.
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.
Journal of Proteome Research|September 7, 2016
Relative Abundance of apoE and Aβ1-42 Associated with Abnormal Prion Protein Differs between Creutzfeldt-Jakob Disease SubtypesRoger A Moore, Young Pyo Choi, Mark W Head, et al.
The American Journal of Pathology|December 26, 2003
Peripheral tissue involvement in sporadic, iatrogenic, and variant Creutzfeldt-Jakob disease: an immunohistochemical, quantitative, and biochemical studyMark W Head, Diane Ritchie, Nadine Smith, et al.
The Journal of General Virology|February 28, 2007
Abnormal prion protein in the pituitary in sporadic and variant Creutzfeldt-Jakob diseaseAlexander H Peden, Diane L Ritchie, Hafsana P Uddin, et al.
Plos Pathogens|February 4, 2016
The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease PatientsRoger A Moore, Mark W Head, James W Ironside, et al.
Journal of Translational Medicine|September 1, 2007
Application of Atomic Dielectric Resonance Spectroscopy for the screening of blood samples from patients with clinical variant and sporadic CJDTimothy J Fagge, G Robin Barclay, G Colin Stove, et al.
The American Journal of Pathology|January 10, 2006
Detection of type 1 prion protein in variant Creutzfeldt-Jakob diseaseHelen M Yull, Diane L Ritchie, Jan P M Langeveld, et al.
Brain Pathology (Zurich, Switzerland)|May 30, 2008
An antibody to the aggregated synthetic prion protein peptide (PrP106-126) selectively recognizes disease-associated prion protein (PrP) from human brain specimensMichael Jones, Darren Wight, Victoria McLoughlin, et al.
Pageof 7

Showing results (41-50 of 68) with videos related to

Sort By:
Pageof 7
Acta Neuropathologica Communications|October 22, 2014
The prion protein protease sensitivity, stability and seeding activity in variably protease sensitive prionopathy brain tissue suggests molecular overlaps with sporadic Creutzfeldt-Jakob diseaseAlexander H Peden, Deep P Sarode, Carl R Mulholland, et al.
Acta Neuropathologica|November 5, 2016
UK Iatrogenic Creutzfeldt-Jakob disease: investigating human prion transmission across genotypic barriers using human tissue-based and molecular approachesDiane L Ritchie, Marcelo A Barria, Alexander H Peden, et al.
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.
Journal of Proteome Research|September 7, 2016
Relative Abundance of apoE and Aβ1-42 Associated with Abnormal Prion Protein Differs between Creutzfeldt-Jakob Disease SubtypesRoger A Moore, Young Pyo Choi, Mark W Head, et al.
The American Journal of Pathology|December 26, 2003
Peripheral tissue involvement in sporadic, iatrogenic, and variant Creutzfeldt-Jakob disease: an immunohistochemical, quantitative, and biochemical studyMark W Head, Diane Ritchie, Nadine Smith, et al.
The Journal of General Virology|February 28, 2007
Abnormal prion protein in the pituitary in sporadic and variant Creutzfeldt-Jakob diseaseAlexander H Peden, Diane L Ritchie, Hafsana P Uddin, et al.
Plos Pathogens|February 4, 2016
The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease PatientsRoger A Moore, Mark W Head, James W Ironside, et al.
Journal of Translational Medicine|September 1, 2007
Application of Atomic Dielectric Resonance Spectroscopy for the screening of blood samples from patients with clinical variant and sporadic CJDTimothy J Fagge, G Robin Barclay, G Colin Stove, et al.
The American Journal of Pathology|January 10, 2006
Detection of type 1 prion protein in variant Creutzfeldt-Jakob diseaseHelen M Yull, Diane L Ritchie, Jan P M Langeveld, et al.
Brain Pathology (Zurich, Switzerland)|May 30, 2008
An antibody to the aggregated synthetic prion protein peptide (PrP106-126) selectively recognizes disease-associated prion protein (PrP) from human brain specimensMichael Jones, Darren Wight, Victoria McLoughlin, et al.
Pageof 7