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Scientific Reports|January 25, 2020
Author Correction: Brain targeting of 9c,11t-Conjugated Linoleic Acid, a natural calpain inhibitor, preserves memory and reduces Aβ and P25 accumulation in 5XFAD miceOrli Binyamin, Keren Nitzan, Kati Frid, et al.
Archives of Neurology|June 11, 2008
Induced neuroprotection independently from PrPSc accumulation in a mouse model for prion disease treated with simvastatinYaron Haviv, Dana Avrahami, Haim Ovadia, et al.
Neurobiology of Aging|March 2, 2018
Autologous neural progenitor cell transplantation into newborn mice modeling for E200K genetic prion disease delays disease progressionKati Frid, Orli Binyamin, Nina Fainstein, et al.
Biochemical and Biophysical Research Communications|November 26, 2003
Novel heparan mimetics potently inhibit the scrapie prion protein and its endocytosisOshrat Schonberger, Lior Horonchik, Ruth Gabizon, et al.
Neuro-Degenerative Diseases|September 7, 2006
Urine from scrapie-infected hamsters comprises low levels of prion infectivityZehavit Kariv-Inbal, Tamir Ben-Hur, Nikolaos C Grigoriadis, et al.
Molecules (Basel, Switzerland)|May 14, 2022
Nano-PSO Administration Attenuates Cognitive and Neuronal Deficits Resulting from Traumatic Brain InjuryDoaa Qubty, Kati Frid, Meirav Har-Even, et al.
Annals of Clinical and Translational Neurology|August 15, 2015
Aggregation of MBP in chronic demyelinationKati Frid, Ofira Einstein, Yael Friedman-Levi, et al.
Journal of Neuroscience Research|May 15, 2008
Virus-induced alterations of membrane lipids affect the incorporation of PrP Sc into cellsDana Avrahami, Yael Dayan-Amouyal, Saar Tal, et al.
Neurobiology of Disease|December 27, 2011
Copper is toxic to PrP-ablated mice and exacerbates disease in a mouse model of E200K genetic prion diseaseTamar Canello, Yael Friedman-Levi, Michal Mizrahi, et al.
Journal of Virology|July 13, 2007
Fatal neurological disease in scrapie-infected mice induced for experimental autoimmune encephalomyelitisYael Friedman-Levi, Haim Ovadia, Romana Hoftberger, et al.
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