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Showing results (191-200 of 203) with videos related to

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Annals of Neurology|June 1, 1996
Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob diseaseP Parchi, R Castellani, S Capellari, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1998
Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker diseaseP Parchi, S G Chen, P Brown, et al.
Annals of Neurology|October 12, 2000
Sporadic fatal insomnia: a case studyF Scaravilli, R J Cordery, H Kretzschmar, et al.
European Journal of Biochemistry|April 12, 2000
Functional and structural differences between the prion protein from two alleles prnp(a) and prnp(b) of mouseD R Brown, I K Iordanova, B S Wong, et al.
Nature Medicine|September 1, 1997
Allelic origin of the abnormal prion protein isoform in familial prion diseasesS G Chen, P Parchi, P Brown, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 22, 1998
Prion protein expression in different species: analysis with a panel of new mAbsG Zanusso, D Liu, S Ferrari, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 30, 2000
Genetic influence on the structural variations of the abnormal prion proteinP Parchi, W Zou, W Wang, et al.
Nature Medicine|April 15, 1999
Tau gene mutation in familial progressive subcortical gliosisM Goedert, M G Spillantini, R A Crowther, et al.
Molecular and Cellular Neurosciences|April 21, 2001
Induction of HO-1 and NOS in doppel-expressing mice devoid of PrP: implications for doppel functionB S Wong, T Liu, D Paisley, et al.
Cellular and Molecular Life Sciences : CMLS|January 15, 2008
Accessibility of a critical prion protein region involved in strain recognition and its implications for the early detection of prionsJ Yuan, Z Dong, J-P Guo, et al.
Pageof 21

Showing results (191-200 of 203) with videos related to

Sort By:
Pageof 21
Annals of Neurology|June 1, 1996
Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob diseaseP Parchi, R Castellani, S Capellari, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1998
Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker diseaseP Parchi, S G Chen, P Brown, et al.
Annals of Neurology|October 12, 2000
Sporadic fatal insomnia: a case studyF Scaravilli, R J Cordery, H Kretzschmar, et al.
European Journal of Biochemistry|April 12, 2000
Functional and structural differences between the prion protein from two alleles prnp(a) and prnp(b) of mouseD R Brown, I K Iordanova, B S Wong, et al.
Nature Medicine|September 1, 1997
Allelic origin of the abnormal prion protein isoform in familial prion diseasesS G Chen, P Parchi, P Brown, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 22, 1998
Prion protein expression in different species: analysis with a panel of new mAbsG Zanusso, D Liu, S Ferrari, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 30, 2000
Genetic influence on the structural variations of the abnormal prion proteinP Parchi, W Zou, W Wang, et al.
Nature Medicine|April 15, 1999
Tau gene mutation in familial progressive subcortical gliosisM Goedert, M G Spillantini, R A Crowther, et al.
Molecular and Cellular Neurosciences|April 21, 2001
Induction of HO-1 and NOS in doppel-expressing mice devoid of PrP: implications for doppel functionB S Wong, T Liu, D Paisley, et al.
Cellular and Molecular Life Sciences : CMLS|January 15, 2008
Accessibility of a critical prion protein region involved in strain recognition and its implications for the early detection of prionsJ Yuan, Z Dong, J-P Guo, et al.
Pageof 21