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R Gabizon

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Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|March 29, 1994
Mutation in codon 200 and polymorphism in codon 129 of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob diseaseR Gabizon, H Rosenman, Z Meiner, et al.
Progress in Clinical and Biological Research|January 1, 1989
Immunoaffinity purification and neutralization of scrapie prionsR Gabizon, M P McKinley, D Groth, et al.
Annals of Neurology|February 9, 2000
Creutzfeldt-Jakob disease profile in patients homozygous for the PRNP E200K mutationE S Simon, E Kahana, J Chapman, et al.
The European Journal of Neuroscience|February 19, 2008
Cellular prion protein co-localizes with nAChR beta4 subunit in brain and gastrointestinal tractS Petrakis, T Irinopoulou, C H Panagiotidis, et al.
Molecular Medicine (Cambridge, Mass.)|September 1, 1995
Complete penetrance of Creutzfeldt-Jakob disease in Libyan Jews carrying the E200K mutation in the prion protein geneS Spudich, J A Mastrianni, M Wrensch, et al.
Cell|October 6, 1995
Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another proteinG C Telling, M Scott, J Mastrianni, et al.
The New England Journal of Medicine|April 18, 1991
Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob diseaseK Hsiao, Z Meiner, E Kahana, et al.
Science (New York, N.Y.)|December 20, 1996
Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversityG C Telling, P Parchi, S J DeArmond, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 21, 1995
Prion protein (PrP) synthetic peptides induce cellular PrP to acquire properties of the scrapie isoformK Kaneko, D Peretz, K M Pan, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|March 29, 1994
Mutation in codon 200 and polymorphism in codon 129 of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob diseaseR Gabizon, H Rosenman, Z Meiner, et al.
Progress in Clinical and Biological Research|January 1, 1989
Immunoaffinity purification and neutralization of scrapie prionsR Gabizon, M P McKinley, D Groth, et al.
Annals of Neurology|February 9, 2000
Creutzfeldt-Jakob disease profile in patients homozygous for the PRNP E200K mutationE S Simon, E Kahana, J Chapman, et al.
The European Journal of Neuroscience|February 19, 2008
Cellular prion protein co-localizes with nAChR beta4 subunit in brain and gastrointestinal tractS Petrakis, T Irinopoulou, C H Panagiotidis, et al.
Molecular Medicine (Cambridge, Mass.)|September 1, 1995
Complete penetrance of Creutzfeldt-Jakob disease in Libyan Jews carrying the E200K mutation in the prion protein geneS Spudich, J A Mastrianni, M Wrensch, et al.
Cell|October 6, 1995
Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another proteinG C Telling, M Scott, J Mastrianni, et al.
The New England Journal of Medicine|April 18, 1991
Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob diseaseK Hsiao, Z Meiner, E Kahana, et al.
Science (New York, N.Y.)|December 20, 1996
Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversityG C Telling, P Parchi, S J DeArmond, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 21, 1995
Prion protein (PrP) synthetic peptides induce cellular PrP to acquire properties of the scrapie isoformK Kaneko, D Peretz, K M Pan, et al.
Pageof 5