These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
154 related articles for article (PubMed ID: 8576163)
1. Mutant and infectious prion proteins display common biochemical properties in cultured cells. Lehmann S; Harris DA J Biol Chem; 1996 Jan; 271(3):1633-7. PubMed ID: 8576163 [TBL] [Abstract][Full Text] [Related]
2. Two mutant prion proteins expressed in cultured cells acquire biochemical properties reminiscent of the scrapie isoform. Lehmann S; Harris DA Proc Natl Acad Sci U S A; 1996 May; 93(11):5610-4. PubMed ID: 8643624 [TBL] [Abstract][Full Text] [Related]
3. Expression of wild-type and V210I mutant prion protein in human neuroblastoma cells. Vetrugno V; Malchow M; Liu Q; Marziali G; Battistini A; Pocchiari M Neurosci Lett; 1999 Jul; 270(1):41-4. PubMed ID: 10454141 [TBL] [Abstract][Full Text] [Related]
4. Identification of intermediate steps in the conversion of a mutant prion protein to a scrapie-like form in cultured cells. Daude N; Lehmann S; Harris DA J Biol Chem; 1997 Apr; 272(17):11604-12. PubMed ID: 9111077 [TBL] [Abstract][Full Text] [Related]
5. Prion peptide 106-126 as a model for prion replication and neurotoxicity. Singh N; Gu Y; Bose S; Kalepu S; Mishra RS; Verghese S Front Biosci; 2002 Apr; 7():a60-71. PubMed ID: 11897566 [TBL] [Abstract][Full Text] [Related]
6. Prion proteins carrying pathogenic mutations are resistant to phospholipase cleavage of their glycolipid anchors. Narwa R; Harris DA Biochemistry; 1999 Jul; 38(27):8770-7. PubMed ID: 10393552 [TBL] [Abstract][Full Text] [Related]
7. Attempts to convert the cellular prion protein into the scrapie isoform in cell-free systems. Raeber AJ; Borchelt DR; Scott M; Prusiner SB J Virol; 1992 Oct; 66(10):6155-63. PubMed ID: 1356161 [TBL] [Abstract][Full Text] [Related]
8. A 60-kDa prion protein (PrP) with properties of both the normal and scrapie-associated forms of PrP. Priola SA; Caughey B; Wehrly K; Chesebro B J Biol Chem; 1995 Feb; 270(7):3299-305. PubMed ID: 7852415 [TBL] [Abstract][Full Text] [Related]
9. Prion protein with an E200K mutation displays properties similar to those of the cellular isoform PrP(C). Rosenmann H; Talmor G; Halimi M; Yanai A; Gabizon R; Meiner Z J Neurochem; 2001 Mar; 76(6):1654-62. PubMed ID: 11259483 [TBL] [Abstract][Full Text] [Related]
10. Scrapie susceptibility-linked polymorphisms modulate the in vitro conversion of sheep prion protein to protease-resistant forms. Bossers A; Belt PBGM ; Raymond GJ; Caughey B; de Vries R; Smits MA Proc Natl Acad Sci U S A; 1997 May; 94(10):4931-6. PubMed ID: 9144167 [TBL] [Abstract][Full Text] [Related]
11. Sheep scrapie susceptibility-linked polymorphisms do not modulate the initial binding of cellular to disease-associated prion protein prior to conversion. Rigter A; Bossers A J Gen Virol; 2005 Sep; 86(Pt 9):2627-2634. PubMed ID: 16099922 [TBL] [Abstract][Full Text] [Related]
12. A mutant prion protein displays an aberrant membrane association when expressed in cultured cells. Lehmann S; Harris DA J Biol Chem; 1995 Oct; 270(41):24589-97. PubMed ID: 7592679 [TBL] [Abstract][Full Text] [Related]
13. Species specificity in the cell-free conversion of prion protein to protease-resistant forms: a model for the scrapie species barrier. Kocisko DA; Priola SA; Raymond GJ; Chesebro B; Lansbury PT; Caughey B Proc Natl Acad Sci U S A; 1995 Apr; 92(9):3923-7. PubMed ID: 7732006 [TBL] [Abstract][Full Text] [Related]
14. Insoluble wild-type and protease-resistant mutant prion protein in brains of patients with inherited prion disease. Gabizon R; Telling G; Meiner Z; Halimi M; Kahana I; Prusiner SB Nat Med; 1996 Jan; 2(1):59-64. PubMed ID: 8564843 [TBL] [Abstract][Full Text] [Related]
15. Prion diseases of the central nervous system. Prusiner SB; DeArmond SJ Monogr Pathol; 1990; (32):86-122. PubMed ID: 2192281 [TBL] [Abstract][Full Text] [Related]
16. Cell-free formation of protease-resistant prion protein. Kocisko DA; Come JH; Priola SA; Chesebro B; Raymond GJ; Lansbury PT; Caughey B Nature; 1994 Aug; 370(6489):471-4. PubMed ID: 7913989 [TBL] [Abstract][Full Text] [Related]
17. Non-genetic propagation of strain-specific properties of scrapie prion protein. Bessen RA; Kocisko DA; Raymond GJ; Nandan S; Lansbury PT; Caughey B Nature; 1995 Jun; 375(6533):698-700. PubMed ID: 7791905 [TBL] [Abstract][Full Text] [Related]
18. Biochemical properties of protease resistant prion protein PrPsc in natural sheep scrapie. Madec JY; Vanier A; Dorier A; Bernillon J; Belli P; Baron T Arch Virol; 1997; 142(8):1603-12. PubMed ID: 9672622 [TBL] [Abstract][Full Text] [Related]
19. Intracellular accumulation of the cellular prion protein after mutagenesis of its Asn-linked glycosylation sites. Rogers M; Taraboulos A; Scott M; Groth D; Prusiner SB Glycobiology; 1990 Sep; 1(1):101-9. PubMed ID: 1983782 [TBL] [Abstract][Full Text] [Related]
20. Sulfated glycans stimulate endocytosis of the cellular isoform of the prion protein, PrPC, in cultured cells. Shyng SL; Lehmann S; Moulder KL; Harris DA J Biol Chem; 1995 Dec; 270(50):30221-9. PubMed ID: 8530433 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]