Similar articles for PMID: 8105481

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1

Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitro.

Tagliavini F, Prelli F, Verga L, Giaccone G, Sarma R, Gorevic P, Ghetti B, Passerini F, Ghibaudi E, Forloni G, et al. Tagliavini F, et al. Proc Natl Acad Sci U S A. 1993 Oct 15;90(20):9678-82. doi: 10.1073/pnas.90.20.9678. Proc Natl Acad Sci U S A. 1993. PMID: 8105481 Free PMC article.

2

Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred.

Giaccone G, Verga L, Bugiani O, Frangione B, Serban D, Prusiner SB, Farlow MR, Ghetti B, Tagliavini F. Giaccone G, et al. Proc Natl Acad Sci U S A. 1992 Oct 1;89(19):9349-53. doi: 10.1073/pnas.89.19.9349. Proc Natl Acad Sci U S A. 1992. PMID: 1357663 Free PMC article.

3

Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58.

Tagliavini F, Prelli F, Ghiso J, Bugiani O, Serban D, Prusiner SB, Farlow MR, Ghetti B, Frangione B. Tagliavini F, et al. EMBO J. 1991 Mar;10(3):513-9. doi: 10.1002/j.1460-2075.1991.tb07977.x. EMBO J. 1991. PMID: 1672107 Free PMC article.

4

Structural properties of Gerstmann-Straussler-Scheinker disease amyloid protein.

Salmona M, Morbin M, Massignan T, Colombo L, Mazzoleni G, Capobianco R, Diomede L, Thaler F, Mollica L, Musco G, Kourie JJ, Bugiani O, Sharma D, Inouye H, Kirschner DA, Forloni G, Tagliavini F. Salmona M, et al. J Biol Chem. 2003 Nov 28;278(48):48146-53. doi: 10.1074/jbc.M307295200. Epub 2003 Sep 11. J Biol Chem. 2003. PMID: 12970341 Free article.

5

Aggregation/fibrillogenesis of recombinant human prion protein and Gerstmann-Sträussler-Scheinker disease peptides in the presence of metal ions.

Ricchelli F, Buggio R, Drago D, Salmona M, Forloni G, Negro A, Tognon G, Zatta P. Ricchelli F, et al. Biochemistry. 2006 May 30;45(21):6724-32. doi: 10.1021/bi0601454. Biochemistry. 2006. PMID: 16716083

6

Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele.

Tagliavini F, Prelli F, Porro M, Rossi G, Giaccone G, Farlow MR, Dlouhy SR, Ghetti B, Bugiani O, Frangione B. Tagliavini F, et al. Cell. 1994 Nov 18;79(4):695-703. doi: 10.1016/0092-8674(94)90554-1. Cell. 1994. PMID: 7954833

7

A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117V.

Tagliavini F, Lievens PM, Tranchant C, Warter JM, Mohr M, Giaccone G, Perini F, Rossi G, Salmona M, Piccardo P, Ghetti B, Beavis RC, Bugiani O, Frangione B, Prelli F. Tagliavini F, et al. J Biol Chem. 2001 Feb 23;276(8):6009-15. doi: 10.1074/jbc.M007062200. Epub 2000 Nov 21. J Biol Chem. 2001. PMID: 11087738 Free article.

8

Gerstmann-Sträussler-Scheinker disease (PRNP P102L): amyloid deposits are best recognized by antibodies directed to epitopes in PrP region 90-165.

Piccardo P, Ghetti B, Dickson DW, Vinters HV, Giaccone G, Bugiani O, Tagliavini F, Young K, Dlouhy SR, Seiler C, et al. Piccardo P, et al. J Neuropathol Exp Neurol. 1995 Nov;54(6):790-801. doi: 10.1097/00005072-199511000-00006. J Neuropathol Exp Neurol. 1995. PMID: 7595652

9

Prion protein amyloidosis.

Ghetti B, Piccardo P, Frangione B, Bugiani O, Giaccone G, Young K, Prelli F, Farlow MR, Dlouhy SR, Tagliavini F. Ghetti B, et al. Brain Pathol. 1996 Apr;6(2):127-45. doi: 10.1111/j.1750-3639.1996.tb00796.x. Brain Pathol. 1996. PMID: 8737929 Review.

10

Neurotoxic and gliotrophic activity of a synthetic peptide homologous to Gerstmann-Sträussler-Scheinker disease amyloid protein.

Fioriti L, Angeretti N, Colombo L, De Luigi A, Colombo A, Manzoni C, Morbin M, Tagliavini F, Salmona M, Chiesa R, Forloni G. Fioriti L, et al. J Neurosci. 2007 Feb 14;27(7):1576-83. doi: 10.1523/JNEUROSCI.5145-06.2007. J Neurosci. 2007. PMID: 17301166 Free PMC article.

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