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4. Protein misfolding and prion diseases. Cohen FE J Mol Biol; 1999 Oct; 293(2):313-20. PubMed ID: 10550211 [TBL] [Abstract][Full Text] [Related]
5. Human prion diseases: molecular and clinical aspects. Glatzel M; Stoeck K; Seeger H; Lührs T; Aguzzi A Arch Neurol; 2005 Apr; 62(4):545-52. PubMed ID: 15824251 [TBL] [Abstract][Full Text] [Related]
6. Prions: protein aggregation and infectious diseases. Aguzzi A; Calella AM Physiol Rev; 2009 Oct; 89(4):1105-52. PubMed ID: 19789378 [TBL] [Abstract][Full Text] [Related]
7. Early and persistent sensory-psychiatric symptoms in an inherited prion disease with a PrP P105L mutation. Shiraishi A; Mizusawa H; Yamada M J Neurol; 2002 Dec; 249(12):1740-1. PubMed ID: 12529802 [No Abstract] [Full Text] [Related]
9. On the track of the white tiger: pigmentation could be linked to prion diseases, and location explains why. Herrero Hernández E Med Hypotheses; 2009 Sep; 73(3):309-11. PubMed ID: 19423237 [TBL] [Abstract][Full Text] [Related]
11. [Transmissible spongiform encephalopathies (prion diseases)--molecular principles and in vitro models]. Kretzschmar H Wien Med Wochenschr; 1998; 148(4):67-73. PubMed ID: 9611345 [TBL] [Abstract][Full Text] [Related]
12. [The mystery of prion proteins: from neurodegenerative diseases to the biology of reproduction]. Peoc'h K Ann Biol Clin (Paris); 2005; 63(2):121-6. PubMed ID: 15771969 [TBL] [Abstract][Full Text] [Related]
13. Canadians find marker for prion diseases. Crabb C Bull World Health Organ; 2003; 81(7):548-9. PubMed ID: 12973651 [No Abstract] [Full Text] [Related]
14. Molecular biology and genetics of prion diseases. Prusiner SB Cold Spring Harb Symp Quant Biol; 1996; 61():473-93. PubMed ID: 9246475 [No Abstract] [Full Text] [Related]
15. Altered circadian activity rhythms and sleep in mice devoid of prion protein. Tobler I; Gaus SE; Deboer T; Achermann P; Fischer M; Rülicke T; Moser M; Oesch B; McBride PA; Manson JC Nature; 1996 Apr; 380(6575):639-42. PubMed ID: 8602267 [TBL] [Abstract][Full Text] [Related]
16. Prion disease. Buono LM Int Ophthalmol Clin; 2007; 47(4):121-9, ix. PubMed ID: 18049285 [No Abstract] [Full Text] [Related]
18. [Molecular bases of prion diseases]. Rać M; Rać M Ann Acad Med Stetin; 2006; 52(3):5-13. PubMed ID: 17385343 [TBL] [Abstract][Full Text] [Related]
19. Influence of amino acid substitutions related to inherited human prion diseases on the thermodynamic stability of the cellular prion protein. Liemann S; Glockshuber R Biochemistry; 1999 Mar; 38(11):3258-67. PubMed ID: 10079068 [TBL] [Abstract][Full Text] [Related]
20. A hypothesis on prion disorders: are infectious, inherited, and sporadic causes so distinct? Fornai F; Ferrucci M; Gesi M; Bandettini di Poggio A; Giorgi FS; Biagioni F; Paparelli A Brain Res Bull; 2006 Mar; 69(2):95-100. PubMed ID: 16533656 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]