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F Wadsworth

Showing results (91-100 of 137) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|July 28, 2010
Spontaneous generation of mammalian prionsJulie A Edgeworth, Nathalie Gros, Jack Alden, et al.
The Japanese Journal of Antibiotics|August 1, 1980
The intravenous toxicity of dibekacin sulphate (DKB) to female beagle dogsR W James, P F Wadsworth, H Chesterman, et al.
Lancet (London, England)|December 13, 2006
Clinical presentation and pre-mortem diagnosis of variant Creutzfeldt-Jakob disease associated with blood transfusion: a case reportStephen J Wroe, Suvankar Pal, Durrenajaf Siddique, et al.
Journal of the Neurological Sciences|February 7, 2018
Experimental sheep BSE prions generate the vCJD phenotype when serially passaged in transgenic mice expressing human prion proteinSusan Joiner, Emmanuel A Asante, Jacqueline M Linehan, et al.
Open Biology|November 17, 2017
Soluble Aβ aggregates can inhibit prion propagationClaire J Sarell, Emma Quarterman, Daniel C-M Yip, et al.
Journal of Environmental Pathology and Toxicology|January 1, 1979
Safety evaluation of toothpaste containing chloroform. III. Long-term study in beagle dogsR Heywood, R J Sortwell, P R Noel, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|October 14, 2008
Central and peripheral pathology of kuru: pathological analysis of a recent case and comparison with other forms of human prion diseaseSebastian Brandner, Jerome Whitfield, Ken Boone, et al.
Plos Pathogens|October 3, 2013
Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion proteinEmmanuel A Asante, Jacqueline M Linehan, Michelle Smidak, et al.
Brain : a Journal of Neurology|April 7, 2006
Phenotypic heterogeneity in inherited prion disease (P102L) is associated with differential propagation of protease-resistant wild-type and mutant prion proteinJonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.
The Journal of General Virology|February 17, 2009
Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteinsEmmanuel A Asante, Ian Gowland, Andrew Grimshaw, et al.
Pageof 14

Showing results (91-100 of 137) with videos related to

Sort By:
Pageof 14
Proceedings of the National Academy of Sciences of the United States of America|July 28, 2010
Spontaneous generation of mammalian prionsJulie A Edgeworth, Nathalie Gros, Jack Alden, et al.
The Japanese Journal of Antibiotics|August 1, 1980
The intravenous toxicity of dibekacin sulphate (DKB) to female beagle dogsR W James, P F Wadsworth, H Chesterman, et al.
Lancet (London, England)|December 13, 2006
Clinical presentation and pre-mortem diagnosis of variant Creutzfeldt-Jakob disease associated with blood transfusion: a case reportStephen J Wroe, Suvankar Pal, Durrenajaf Siddique, et al.
Journal of the Neurological Sciences|February 7, 2018
Experimental sheep BSE prions generate the vCJD phenotype when serially passaged in transgenic mice expressing human prion proteinSusan Joiner, Emmanuel A Asante, Jacqueline M Linehan, et al.
Open Biology|November 17, 2017
Soluble Aβ aggregates can inhibit prion propagationClaire J Sarell, Emma Quarterman, Daniel C-M Yip, et al.
Journal of Environmental Pathology and Toxicology|January 1, 1979
Safety evaluation of toothpaste containing chloroform. III. Long-term study in beagle dogsR Heywood, R J Sortwell, P R Noel, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|October 14, 2008
Central and peripheral pathology of kuru: pathological analysis of a recent case and comparison with other forms of human prion diseaseSebastian Brandner, Jerome Whitfield, Ken Boone, et al.
Plos Pathogens|October 3, 2013
Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion proteinEmmanuel A Asante, Jacqueline M Linehan, Michelle Smidak, et al.
Brain : a Journal of Neurology|April 7, 2006
Phenotypic heterogeneity in inherited prion disease (P102L) is associated with differential propagation of protease-resistant wild-type and mutant prion proteinJonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.
The Journal of General Virology|February 17, 2009
Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteinsEmmanuel A Asante, Ian Gowland, Andrew Grimshaw, et al.
Pageof 14