Reference List:
1999
- Protein misfolding and prion diseases.
Cohen FE.
J Mol Biol 1999, 293: 313-20 Medline
- Structural Studies of Prion Proteins.
Cohen FE, Prusiner SB.
In Prion Biology and Diseases Cold Spring Harbor Laboratory Press 1999 pp. 191-228
- Evolutionary, mechanistic, and predictive analyses of the hydroxymethyldihydropterin pyrophosphokinase family of proteins.
Gerloff DL, Cannarozzi GM, Joachimiak M, Cohen FE, Schreiber D, Benner SA.
Biochem Biophys Res Commun 1999, 254: 70-6 Medline
- Thermodynamics of model prions and its implications for the problem of prion protein folding.
Harrison PM, Chan HS, Prusiner SB, Cohen FE.
J Mol Biol 1999, 286: 593-606 Medline
- Antibody binding defines a structure for an epitope that participates in the PrPC-->PrPSc conformational change.
Kanyo ZF, Pan KM, Williamson RA, Burton DR, Prusiner SB, Fletterick RJ, Cohen FE.
J Mol Biol 1999, 293: 855-63 Medline
- Solution structure of Syrian hamster prion protein rPrP(90-231).
Liu H, Farr-Jones S, Ulyanov NB, Llinas M, Marqusee S, Groth D, Cohen FE, Prusiner SB, James TL.
Biochemistry 1999, 38: 5362-77 Medline
- Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppel.
Moore RC, Lee IY, Silverman GL, Harrison PM, Strome R, Heinrich C, Karunaratne A, Pasternak SH, Chishti MA, Liang Y, Mastrangelo P, Wang K, Smit AF, Katamine S, Carlson GA, Cohen FE, Prusiner SB, Melton DW, Tremblay P, Hood LE, Westaway D.
J Mol Biol 1999, 292: 797-817 Medline
- Transgenetic Approaches to Studies of Prion Diseases.
Prusiner SB, Cohen FE, DeArmond SJ.
In Prion Diseases: Current State and Perspectives in Prion Research ed H Kretzschmar and D Reisner Chapman and Hall Weinheim, Germany 1999 pp..
- Some Strategies and Methods for the Study of Prions
Prusiner SB, Kaneko K, Serban H, Cohen FE, Safar J, Riesner D.
In Prion Biology and Diseases Cold Spring Harbor Laboratory Press 1999 pp. 653-716
- Cell Biology of Prions
Prusiner SB, Peter P, Kaneko K, Taraboulos A, Lingappa V, Cohen FE, DeArmond SJ.
In Prion Biology and Diseases Cold Spring Harbor Laboratory Press 1999 pp. 349-392
- The Prion Diseases
Prusiner SB, Safar J, Cohen FE, DeArmond SJ.
In Alzheimer Disease Liincott Williams & Wilkins 1999 pp. 161-180
- High-resolution autoreactive epitope mapping and structural modeling of the 65 kDa form of human glutamic acid decarboxylase.
Schwartz HL, Chandonia JM, Kash SF, Kanaani J, Tunnell E, Domingo A, Cohen FE, Banga JP, Madec AM, Richter W, Baekkeskov S.
J Mol Biol 1999, 287: 983-99 Medline
- Prion protein of 106 residues creates an artifical transmission barrier for prion replication in transgenic mice.
Supattapone S, Bosque P, Muramoto T, Wille H, Aagaard C, Peretz D, Nguyen HO, Heinrich C, Torchia M, Safar J, Cohen FE, DeArmond SJ, Prusiner SB, Scott M.
Cell 1999, 96: 869-78 Medline
- Elimination of prions by branched polyamines and implications for therapeutics.
Supattapone S, Nguyen HO, Cohen FE, Prusiner SB, Scott MR.
Proc Natl Acad Sci U S A 1999, 96: 14529-34 Medline
- Copper binding to the prion protein: structural implications of four identical cooperative binding sites.
Viles JH, Cohen FE, Prusiner SB, Goodin DB, Wright PE, Dyson HJ.
Proc Natl Acad Sci U S A 1999, 96: 2042-7 Medline
- Conformational attractors on the Ramachandran map.
Walther D, Cohen FE.
Acta Crystallogr D Biol Crystallogr 1999, 55 ( Pt 2): 506-17 Medline