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Journal of Virological Methods|January 3, 2006
Prion urine comprises a glycosaminoglycan-light chain IgG complex that can be stained by Congo redMichele Halimi, Yael Dayan-Amouyal, Zehavit Kariv-Inbal, et al.Plos Pathogens|July 14, 2010
Oxidation of Helix-3 methionines precedes the formation of PK resistant PrPTamar Canello, Kati Frid, Ronen Gabizon, et al.Plos Pathogens|May 4, 2017
Correction: Oxidation of Helix-3 Methionines Precedes the Formation of PK Resistant PrPScTamar Canello, Kati Frid, Ronen Gabizon, et al.Frontiers in Neuroscience|November 29, 2016
Chronic Progressive Neurodegeneration in a Transgenic Mouse Model of Prion DiseaseNina Fainstein, Dvir Dori, Kati Frid, et al.Neurobiology of Disease|June 14, 2005
The metabolism of glycosaminoglycans is impaired in prion diseasesTehila Mayer-Sonnenfeld, Marsha Zeigler, Michele Halimi, et al.Journal of Neuroinflammation|March 23, 2012
Targeting of prion-infected lymphoid cells to the central nervous system accelerates prion infectionYael Friedman-Levi, Romana Hoftberger, Herbert Budka, et al.Biochemistry|October 16, 2002
Protease-sensitive scrapie prion protein in aggregates of heterogeneous sizesSalit Tzaban, Gilgi Friedlander, Oshrat Schonberger, et al.Archives of Biochemistry and Biophysics|April 24, 2009
Detection of oxidized methionine in selected proteins, cellular extracts and blood serums by novel anti-methionine sulfoxide antibodiesDerek B Oien, Tamar Canello, Ruth Gabizon, et al.Journal of Neuroimmunology|February 24, 2024
Granagard administration prolongs the survival of human mesenchymal stem cells transplanted into a mouse model of multiple sclerosisKati Frid, Areen Usmann, Tsipora Markovits-Pachter, et al.Plos Pathogens|November 11, 2011
Fatal prion disease in a mouse model of genetic E200K Creutzfeldt-Jakob diseaseYael Friedman-Levi, Zeev Meiner, Tamar Canello, et al.Pageof 5