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Acta Neurologica Scandinavica
|
April 8, 1998
Identification in Israel of 2 Jewish Creutzfeld-Jakob disease patients with a 178 mutation at their PrP gene
H Rosenmann, J Vardi, Y Finkelstein, et al.
Journal of Cellular Physiology
|
November 1, 1993
Heparin-like molecules bind differentially to prion-proteins and change their intracellular metabolic fate
R Gabizon, Z Meiner, M Halimi, et al.
Journal of Virology
|
August 3, 2001
Copper binding to the PrP isoforms: a putative marker of their conformation and function
Y Shaked, H Rosenmann, N Hijazi, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1988
Immunoaffinity purification and neutralization of scrapie prion infectivity
R Gabizon, M P McKinley, D Groth, et al.
The Journal of Biological Chemistry
|
January 21, 2001
Reconstitution of prion infectivity from solubilized protease-resistant PrP and nonprotein components of prion rods
G M Shaked, Z Meiner, I Avraham, et al.
The Journal of Biological Chemistry
|
June 11, 1999
Protease-resistant and detergent-insoluble prion protein is not necessarily associated with prion infectivity
G M Shaked, G Fridlander, Z Meiner, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1993
Attempts to restore scrapie prion infectivity after exposure to protein denaturants
S B Prusiner, D Groth, A Serban, 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.
Journal of Neurochemistry
|
October 18, 2000
The cellular prion protein colocalizes with the dystroglycan complex in the brain
G I Keshet, O Bar-Peled, D Yaffe, 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 cells
H Ovadia, H Rosenmann, E Shezen, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 49) with videos related to
Sort By:
Page
of 5
Acta Neurologica Scandinavica
|
April 8, 1998
Identification in Israel of 2 Jewish Creutzfeld-Jakob disease patients with a 178 mutation at their PrP gene
H Rosenmann, J Vardi, Y Finkelstein, et al.
Journal of Cellular Physiology
|
November 1, 1993
Heparin-like molecules bind differentially to prion-proteins and change their intracellular metabolic fate
R Gabizon, Z Meiner, M Halimi, et al.
Journal of Virology
|
August 3, 2001
Copper binding to the PrP isoforms: a putative marker of their conformation and function
Y Shaked, H Rosenmann, N Hijazi, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1988
Immunoaffinity purification and neutralization of scrapie prion infectivity
R Gabizon, M P McKinley, D Groth, et al.
The Journal of Biological Chemistry
|
January 21, 2001
Reconstitution of prion infectivity from solubilized protease-resistant PrP and nonprotein components of prion rods
G M Shaked, Z Meiner, I Avraham, et al.
The Journal of Biological Chemistry
|
June 11, 1999
Protease-resistant and detergent-insoluble prion protein is not necessarily associated with prion infectivity
G M Shaked, G Fridlander, Z Meiner, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1993
Attempts to restore scrapie prion infectivity after exposure to protein denaturants
S B Prusiner, D Groth, A Serban, 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.
Journal of Neurochemistry
|
October 18, 2000
The cellular prion protein colocalizes with the dystroglycan complex in the brain
G I Keshet, O Bar-Peled, D Yaffe, 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 cells
H Ovadia, H Rosenmann, E Shezen, et al.
Page
of 5