1[1]Coles H. Nobel rewards prion theory after years of heated debate[J]. Nature,1997,389:529.
2[2]Prusiner S B. Prion disease and the BSE crisis[J]. Science.1997,278:245-251.
3[3]Prusiner S B. Novel proteinaceous infectious particles cause Scrapie[J]. Science.1982,216 (4542):136-140.
4[4]Stahl N, et al. Glycosy linositol phospholipid anchors of the scrapie and cellular prion protein[J]. Biochemistry,1992,31:5043-5053.
5[5]Prusiner S B. The Prion Disease[J]. Scientific American.1995,272:30-37.
6[6]Bessen R A, et al. Non-genetic propagation of stain-specific properties of scrapie prion protein[J]. Nature,1995,375:698-700.
7[7]Cohen F E, et al. Structural clues to prion replication[J]. Science,1994,264:530-531.
8[8]Schtzl H M, et al. Prion protein gene variation among primates[J]. J Mol Biol,1995,245:362-374.
9[9]Hunter N, et al. Restriction fragment length polymorphisms of the scrapie-association fibril protein(PrP) gene and their association with susceptibility to natural scrapie in British sheep[J]. J Gen Virol,1991,72:1287-1292.
10[10]Glover J R,et al. Self-seeded fibers formed by Sup35,the protein Determinant of [PSI+],a heritable prion-like factor of S. cerevisiae [J]. Cell,1997,89:811-819.
2Prusiner,S B.Prion disease and the BSE crifis[J].Scicnce,1997,278:245-251.
3Supattapone S,Bosque P,Muramoto T,et al.Prion protein of 106 residues creates an artificial transmission barrier for prion replication in transgenic mice[J].Cell,1999,96:869-878.
4Liu H,Farr-Jones S,Ulyanov N B,et al.Solution structure of Syrian hamster prion protein rPrP(90-231)[J].Biochemistry,1999,38:5362-5377.