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The Journal of Biological Chemistry|November 5, 1999
A C-terminal-truncated PrP isoform is present in mature spermY Shaked, H Rosenmann, G Talmor, et al.
Acta Neurologica Scandinavica|April 8, 1998
Identification in Israel of 2 Jewish Creutzfeld-Jakob disease patients with a 178 mutation at their PrP geneH Rosenmann, J Vardi, Y Finkelstein, et al.
Journal of Virology|August 3, 2001
Copper binding to the PrP isoforms: a putative marker of their conformation and functionY Shaked, H Rosenmann, N Hijazi, et al.
Neurology|September 26, 1997
Differential allelic expression of PrP mRNA in carriers of the E200K mutationH Rosenmann, M Halimi, I Kahana, et al.
The Journal of Biological Chemistry|July 12, 1996
Effect of scrapie infection on the activity of neuronal nitric-oxide synthase in brain and neuroblastoma cellsH Ovadia, H Rosenmann, E Shezen, et al.
Journal of Neurochemistry|March 22, 2001
Prion protein with an E200K mutation displays properties similar to those of the cellular isoform PrP(C)H Rosenmann, G Talmor, M Halimi, et al.
Acta Neurologica Scandinavica|October 17, 2014
Seizures in E200K familial and sporadic Creutzfeldt-Jakob diseaseS Appel, J Chapman, O S Cohen, et al.
Neurology|October 16, 1999
Preliminary evidence for anticipation in genetic E200K Creutzfeldt-Jakob diseaseH Rosenmann, E Kahana, A D Korczyn, et al.
Neurology|August 1, 1997
Detection of 14-3-3 protein in the CSF of genetic Creutzfeldt-Jakob diseaseH Rosenmann, Z Meiner, E Kahana, et al.
American Journal of Human Genetics|October 1, 1993
Mutation and polymorphism of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease (CJD)R Gabizon, H Rosenmann, Z Meiner, et al.
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