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.
2. Expansion of the octarepeat domain alters the misfolding pathway but not the folding pathway of the prion protein. Leliveld SR; Stitz L; Korth C Biochemistry; 2008 Jun; 47(23):6267-78. PubMed ID: 18473442 [TBL] [Abstract][Full Text] [Related]
3. Post-translational hydroxylation at the N-terminus of the prion protein reveals presence of PPII structure in vivo. Gill AC; Ritchie MA; Hunt LG; Steane SE; Davies KG; Bocking SP; Rhie AG; Bennett AD; Hope J EMBO J; 2000 Oct; 19(20):5324-31. PubMed ID: 11032800 [TBL] [Abstract][Full Text] [Related]
4. Molecular model of an alpha-helical prion protein dimer and its monomeric subunits as derived from chemical cross-linking and molecular modeling calculations. Kaimann T; Metzger S; Kuhlmann K; Brandt B; Birkmann E; Höltje HD; Riesner D J Mol Biol; 2008 Feb; 376(2):582-96. PubMed ID: 18158160 [TBL] [Abstract][Full Text] [Related]
5. Toward the molecular basis of inherited prion diseases: NMR structure of the human prion protein with V210I mutation. Biljan I; Ilc G; Giachin G; Raspadori A; Zhukov I; Plavec J; Legname G J Mol Biol; 2011 Sep; 412(4):660-73. PubMed ID: 21839748 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Core structure of amyloid fibrils formed by residues 106-126 of the human prion protein. Walsh P; Simonetti K; Sharpe S Structure; 2009 Mar; 17(3):417-26. PubMed ID: 19278656 [TBL] [Abstract][Full Text] [Related]
9. Membrane interactions and conformational preferences of human and avian prion N-terminal tandem repeats: the role of copper(II) ions, pH, and membrane mimicking environments. Di Natale G; Pappalardo G; Milardi D; Sciacca MF; Attanasio F; La Mendola D; Rizzarelli E J Phys Chem B; 2010 Nov; 114(43):13830-8. PubMed ID: 20936829 [TBL] [Abstract][Full Text] [Related]
10. Familial prion disease mutation alters the secondary structure of recombinant mouse prion protein: implications for the mechanism of prion formation. Cappai R; Stewart L; Jobling MF; Thyer JM; White AR; Beyreuther K; Collins SJ; Masters CL; Barrow CJ Biochemistry; 1999 Mar; 38(11):3280-4. PubMed ID: 10079070 [TBL] [Abstract][Full Text] [Related]
11. Production, purification and oxidative folding of the mouse recombinant prion protein. Pavlícek A; Bednárová L; Holada K Folia Microbiol (Praha); 2007; 52(4):391-7. PubMed ID: 18062188 [TBL] [Abstract][Full Text] [Related]
12. Molecular modelling indicates that the pathological conformations of prion proteins might be beta-helical. Downing DT; Lazo ND Biochem J; 1999 Oct; 343 Pt 2(Pt 2):453-60. PubMed ID: 10510313 [TBL] [Abstract][Full Text] [Related]
13. Autonomous and reversible folding of a soluble amino-terminally truncated segment of the mouse prion protein. Hornemann S; Glockshuber R J Mol Biol; 1996 Sep; 261(5):614-9. PubMed ID: 8800210 [TBL] [Abstract][Full Text] [Related]
14. Interaction of the 106-126 prion peptide with lipid membranes and potential implication for neurotoxicity. Dupiereux I; Zorzi W; Lins L; Brasseur R; Colson P; Heinen E; Elmoualij B Biochem Biophys Res Commun; 2005 Jun; 331(4):894-901. PubMed ID: 15882962 [TBL] [Abstract][Full Text] [Related]
16. The prion protein: Structural features and related toxic peptides. Ronga L; Tizzano B; Palladino P; Ragone R; Urso E; Maffia M; Ruvo M; Benedetti E; Rossi F Chem Biol Drug Des; 2006 Sep; 68(3):139-47. PubMed ID: 17062011 [TBL] [Abstract][Full Text] [Related]
17. Hydrogen/deuterium exchange mass spectrometry identifies two highly protected regions in recombinant full-length prion protein amyloid fibrils. Nazabal A; Hornemann S; Aguzzi A; Zenobi R J Mass Spectrom; 2009 Jun; 44(6):965-77. PubMed ID: 19283723 [TBL] [Abstract][Full Text] [Related]
18. The 118-135 peptide of the human prion protein forms amyloid fibrils and induces liposome fusion. Pillot T; Lins L; Goethals M; Vanloo B; Baert J; Vandekerckhove J; Rosseneu M; Brasseur R J Mol Biol; 1997 Dec; 274(3):381-93. PubMed ID: 9405147 [TBL] [Abstract][Full Text] [Related]
19. Evidence that the 127-164 region of prion proteins has two equi-energetic conformations with beta or alpha features. Derreumaux P Biophys J; 2001 Sep; 81(3):1657-65. PubMed ID: 11509378 [TBL] [Abstract][Full Text] [Related]
20. NMR structure of the mouse prion protein domain PrP(121-231). Riek R; Hornemann S; Wider G; Billeter M; Glockshuber R; Wüthrich K Nature; 1996 Jul; 382(6587):180-2. PubMed ID: 8700211 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]