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Otto Windl

Showing results (11-20 of 41) with videos related to

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Acta Neuropathologica|November 24, 2004
Loss of glycosylation associated with the T183A mutation in human prion diseaseE Grasbon-Frodl, Holger Lorenz, U Mann, et al.
Biochemical and Biophysical Research Communications|May 18, 2005
Activation of phosphatidylinositol 3-kinase by cellular prion protein and its role in cell survivalNeville Vassallo, Jochen Herms, Christina Behrens, et al.
Acta Neuropathologica|March 2, 2005
Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragmentSigrun Roeber, Bjarne Krebs, Manuela Neumann, et al.
Annals of Neurology|July 29, 2005
Cerebral gene expression profiles in sporadic Creutzfeldt-Jakob diseaseWei Xiang, Otto Windl, Ingo M Westner, et al.
Plos One|July 23, 2013
Enzymatic formulation capable of degrading scrapie prion under mild digestion conditionsEmeka A Okoroma, Diane Purchase, Hemda Garelick, et al.
Prion|October 9, 2010
Proteomic consequences of expression and pathological conversion of the prion protein in inducible neuroblastoma N2a cellsMonique Provansal, Stéphane Roche, Manuela Pastore, et al.
The Journal of Biological Chemistry|February 4, 2006
Conversion efficiency of bank vole prion protein in vitro is determined by residues 155 and 170, but does not correlate with the high susceptibility of bank voles to sheep scrapie in vivoNiklas Piening, Romolo Nonno, Michele Di Bari, et al.
The Journal of General Virology|March 7, 2009
Ovine PRNP untranslated region and promoter haplotype diversityGinny C Saunders, Saira Cawthraw, Susan J Mountjoy, et al.
Journal of Virology|December 25, 2009
Infection of cell lines with experimental and natural ovine scrapie agentsMichael H Neale, Susan J Mountjoy, Jane C Edwards, et al.
Journal of Virology|September 29, 2004
Identification of differentially expressed genes in scrapie-infected mouse brains by using global gene expression technologyWei Xiang, Otto Windl, Gerda Wünsch, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
Acta Neuropathologica|November 24, 2004
Loss of glycosylation associated with the T183A mutation in human prion diseaseE Grasbon-Frodl, Holger Lorenz, U Mann, et al.
Biochemical and Biophysical Research Communications|May 18, 2005
Activation of phosphatidylinositol 3-kinase by cellular prion protein and its role in cell survivalNeville Vassallo, Jochen Herms, Christina Behrens, et al.
Acta Neuropathologica|March 2, 2005
Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragmentSigrun Roeber, Bjarne Krebs, Manuela Neumann, et al.
Annals of Neurology|July 29, 2005
Cerebral gene expression profiles in sporadic Creutzfeldt-Jakob diseaseWei Xiang, Otto Windl, Ingo M Westner, et al.
Plos One|July 23, 2013
Enzymatic formulation capable of degrading scrapie prion under mild digestion conditionsEmeka A Okoroma, Diane Purchase, Hemda Garelick, et al.
Prion|October 9, 2010
Proteomic consequences of expression and pathological conversion of the prion protein in inducible neuroblastoma N2a cellsMonique Provansal, Stéphane Roche, Manuela Pastore, et al.
The Journal of Biological Chemistry|February 4, 2006
Conversion efficiency of bank vole prion protein in vitro is determined by residues 155 and 170, but does not correlate with the high susceptibility of bank voles to sheep scrapie in vivoNiklas Piening, Romolo Nonno, Michele Di Bari, et al.
The Journal of General Virology|March 7, 2009
Ovine PRNP untranslated region and promoter haplotype diversityGinny C Saunders, Saira Cawthraw, Susan J Mountjoy, et al.
Journal of Virology|December 25, 2009
Infection of cell lines with experimental and natural ovine scrapie agentsMichael H Neale, Susan J Mountjoy, Jane C Edwards, et al.
Journal of Virology|September 29, 2004
Identification of differentially expressed genes in scrapie-infected mouse brains by using global gene expression technologyWei Xiang, Otto Windl, Gerda Wünsch, et al.
Pageof 5