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R Gabizon

Showing results (31-40 of 49) with videos related to

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Neurology|July 1, 1992
Presence of prion protein in peripheral tissues of Libyan Jews with Creutzfeldt-Jakob diseaseZ Meiner, M Halimi, R D Polakiewicz, et al.
The Journal of Biological Chemistry|March 7, 1998
The anti-prion activity of Congo red. Putative mechanismS Caspi, M Halimi, A Yanai, et al.
The Journal of Biological Chemistry|April 5, 1988
Properties of scrapie prion protein liposomesR Gabizon, M P McKinley, D F Groth, et al.
Nature Medicine|January 1, 1996
Insoluble wild-type and protease-resistant mutant prion protein in brains of patients with inherited prion diseaseR Gabizon, G Telling, Z Meiner, et al.
Virology|June 1, 1988
Scrapie prion liposomes and rods exhibit target sizes of 55,000 DaC G Bellinger-Kawahara, E Kempner, D Groth, et al.
Neurology|October 16, 1999
Preliminary evidence for anticipation in genetic E200K Creutzfeldt-Jakob diseaseH Rosenmann, E Kahana, A D Korczyn, et al.
The Journal of Biological Chemistry|June 26, 2001
A protease-resistant prion protein isoform is present in urine of animals and humans affected with prion diseasesG M Shaked, Y Shaked, Z Kariv-Inbal, 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.
Journal of Neuroendocrinology|August 14, 2012
Multiple pathways for high voltage-activated ca(2+) influx in anterior pituitary lactotrophs and somatotrophsA Tzour, E Sosial, T Meir, 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.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
Neurology|July 1, 1992
Presence of prion protein in peripheral tissues of Libyan Jews with Creutzfeldt-Jakob diseaseZ Meiner, M Halimi, R D Polakiewicz, et al.
The Journal of Biological Chemistry|March 7, 1998
The anti-prion activity of Congo red. Putative mechanismS Caspi, M Halimi, A Yanai, et al.
The Journal of Biological Chemistry|April 5, 1988
Properties of scrapie prion protein liposomesR Gabizon, M P McKinley, D F Groth, et al.
Nature Medicine|January 1, 1996
Insoluble wild-type and protease-resistant mutant prion protein in brains of patients with inherited prion diseaseR Gabizon, G Telling, Z Meiner, et al.
Virology|June 1, 1988
Scrapie prion liposomes and rods exhibit target sizes of 55,000 DaC G Bellinger-Kawahara, E Kempner, D Groth, et al.
Neurology|October 16, 1999
Preliminary evidence for anticipation in genetic E200K Creutzfeldt-Jakob diseaseH Rosenmann, E Kahana, A D Korczyn, et al.
The Journal of Biological Chemistry|June 26, 2001
A protease-resistant prion protein isoform is present in urine of animals and humans affected with prion diseasesG M Shaked, Y Shaked, Z Kariv-Inbal, 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.
Journal of Neuroendocrinology|August 14, 2012
Multiple pathways for high voltage-activated ca(2+) influx in anterior pituitary lactotrophs and somatotrophsA Tzour, E Sosial, T Meir, 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.
Pageof 5