Mouse-adapted scrapie strains 139A and ME7 overcome species barrier to induce experimental scrapie in hamsters and changed their pathogenic features

[1] Morales R(2007)The prion strain phenomenon: Molecular basis and unprecedented features Biochim Biophys Acta 1772 681-691

[2] Abid K(1990)Transmissible encephalopathies in animals Can J Vet Res 54 30-37

[3] Soto C(1998)Prions Proc Natl Acad Sci USA 95 13363-13383

[4] Kimberlin RH(2009)Prion Protein Misfolding and Disease Curr Opin Struct Biol 19 14-22

[5] Prusiner SB(2004)Chronic Wasting Disease--Prion Disease in the Wild PLoS Biol 2 e121-1503

[6] Moore RA(2007)Quantifying the risk from ovine BSE and the impact of control strategies Proc Biol Sci 274 1497-1522

[7] Taubner LM(2009)Prion variants, species barriers, generation and propagation J Biol 8 47-265

[8] Priola SA(1991)Molecular biology of prion diseases Science 252 1515-4680

[9] Bunk S(2003)Acquired prion disease: iatrogenic CJD, variant CJD, kuru Br Med Bull 66 255-20

[10] Fryer HR(2001)Chan. Efficient conversion of normal prion protein (PrP) by abnormal hamster PrP is determined by homology at amino acid residue 155 J Virol 75 4673-680

[1] Morales R(2007)The prion strain phenomenon: Molecular basis and unprecedented features Biochim Biophys Acta 1772 681-691

[2] Abid K(1990)Transmissible encephalopathies in animals Can J Vet Res 54 30-37

[3] Soto C(1998)Prions Proc Natl Acad Sci USA 95 13363-13383

[4] Kimberlin RH(2009)Prion Protein Misfolding and Disease Curr Opin Struct Biol 19 14-22

[5] Prusiner SB(2004)Chronic Wasting Disease--Prion Disease in the Wild PLoS Biol 2 e121-1503

[6] Moore RA(2007)Quantifying the risk from ovine BSE and the impact of control strategies Proc Biol Sci 274 1497-1522

[7] Taubner LM(2009)Prion variants, species barriers, generation and propagation J Biol 8 47-265

[8] Priola SA(1991)Molecular biology of prion diseases Science 252 1515-4680

[9] Bunk S(2003)Acquired prion disease: iatrogenic CJD, variant CJD, kuru Br Med Bull 66 255-20

[10] Fryer HR(2001)Chan. Efficient conversion of normal prion protein (PrP) by abnormal hamster PrP is determined by homology at amino acid residue 155 J Virol 75 4673-680