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15. Unraveling the details of prion (con)formation(s): recent advances by mass spectrometry. Principe S; Maras B; Schininà ME; Pocchiari M; Cardone F Curr Opin Drug Discov Devel; 2008 Sep; 11(5):697-707. PubMed ID: 18729021 [TBL] [Abstract][Full Text] [Related]
16. Differential solubility of prions is associated in manifold phenotypes. Kuczius T; Karch H; Groschup MH Mol Cell Neurosci; 2009 Nov; 42(3):226-33. PubMed ID: 19607920 [TBL] [Abstract][Full Text] [Related]
17. A transmembrane form of the prion protein in neurodegenerative disease. Hegde RS; Mastrianni JA; Scott MR; DeFea KA; Tremblay P; Torchia M; DeArmond SJ; Prusiner SB; Lingappa VR Science; 1998 Feb; 279(5352):827-34. PubMed ID: 9452375 [TBL] [Abstract][Full Text] [Related]
18. Oxidation of methionine 216 in sheep and elk prion protein is highly dependent upon the amino acid at position 218 but is not important for prion propagation. Silva CJ; Dynin I; Erickson ML; Requena JR; Balachandran A; Hui C; Onisko BC; Carter JM Biochemistry; 2013 Mar; 52(12):2139-47. PubMed ID: 23458153 [TBL] [Abstract][Full Text] [Related]
19. The use of transgenic mice in the investigation of transmissible spongiform encephalopathies. Weissmann C; Fischer M; Raeber A; Büeler H; Sailer A; Shmerling D; Rülicke T; Brandner S; Aguzzi A Int J Exp Pathol; 1996 Dec; 77(6):283-93. PubMed ID: 9155663 [No Abstract] [Full Text] [Related]
20. Some implications of the prion paradigm: caveat denaturor. Lederberg J JAMA; 1999 Oct; 282(14):1332-3. PubMed ID: 10527177 [No Abstract] [Full Text] [Related] [Next] [New Search]