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Results: 1 to 20 of 72

Similar articles for PubMed (Select 12787080)

1.

Post-transcriptional suppression of pathogenic prion protein expression in Drosophila neurons.

Deleault NR, Dolph PJ, Feany MB, Cook ME, Nishina K, Harris DA, Supattapone S.

J Neurochem. 2003 Jun;85(6):1614-23.

PMID:
12787080
2.

Accelerated accumulation of misfolded prion protein and spongiform degeneration in a Drosophila model of Gerstmann-Sträussler-Scheinker syndrome.

Gavin BA, Dolph MJ, Deleault NR, Geoghegan JC, Khurana V, Feany MB, Dolph PJ, Supattapone S.

J Neurosci. 2006 Nov 29;26(48):12408-14.

3.

Insoluble wild-type and protease-resistant mutant prion protein in brains of patients with inherited prion disease.

Gabizon R, Telling G, Meiner Z, Halimi M, Kahana I, Prusiner SB.

Nat Med. 1996 Jan;2(1):59-64.

PMID:
8564843
4.

Primary myopathy and accumulation of PrPSc-like molecules in peripheral tissues of transgenic mice expressing a prion protein insertional mutation.

Chiesa R, Pestronk A, Schmidt RE, Tourtellotte WG, Ghetti B, Piccardo P, Harris DA.

Neurobiol Dis. 2001 Apr;8(2):279-88.

PMID:
11300723
5.

RNA molecules stimulate prion protein conversion.

Deleault NR, Lucassen RW, Supattapone S.

Nature. 2003 Oct 16;425(6959):717-20.

PMID:
14562104
6.

The AGAAAAGA palindrome in PrP is required to generate a productive PrPSc-PrPC complex that leads to prion propagation.

Norstrom EM, Mastrianni JA.

J Biol Chem. 2005 Jul 22;280(29):27236-43. Epub 2005 May 25.

7.

The role of PrP in health and disease.

Flechsig E, Weissmann C.

Curr Mol Med. 2004 Jun;4(4):337-53. Review.

PMID:
15354865
8.

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 10;47(23):6267-78. doi: 10.1021/bi800253c. Epub 2008 May 13.

PMID:
18473442
10.

Normal prion protein in Drosophila enhances the toxicity of pathogenic polyglutamine proteins and alters susceptibility to oxidative and autophagy signaling modulators.

Park Y, Kim W, Kim AY, Choi HJ, Choi JK, Park N, Koh EK, Seo J, Koh YH.

Biochem Biophys Res Commun. 2011 Jan 14;404(2):638-45. doi: 10.1016/j.bbrc.2010.12.030. Epub 2010 Dec 10.

PMID:
21146501
11.

Insoluble aggregates and protease-resistant conformers of prion protein in uninfected human brains.

Yuan J, Xiao X, McGeehan J, Dong Z, Cali I, Fujioka H, Kong Q, Kneale G, Gambetti P, Zou WQ.

J Biol Chem. 2006 Nov 17;281(46):34848-58. Epub 2006 Sep 20.

12.

In vitro and in vivo neurotoxicity of prion protein oligomers.

Simoneau S, Rezaei H, Salès N, Kaiser-Schulz G, Lefebvre-Roque M, Vidal C, Fournier JG, Comte J, Wopfner F, Grosclaude J, Schätzl H, Lasmézas CI.

PLoS Pathog. 2007 Aug 31;3(8):e125.

13.

Truncated prion protein and Doppel are myelinotoxic in the absence of oligodendrocytic PrPC.

Radovanovic I, Braun N, Giger OT, Mertz K, Miele G, Prinz M, Navarro B, Aguzzi A.

J Neurosci. 2005 May 11;25(19):4879-88.

14.

Disease-related prion protein forms aggresomes in neuronal cells leading to caspase activation and apoptosis.

Kristiansen M, Messenger MJ, Klöhn PC, Brandner S, Wadsworth JD, Collinge J, Tabrizi SJ.

J Biol Chem. 2005 Nov 18;280(46):38851-61. Epub 2005 Sep 12.

15.

Prion protein functions and dysfunction in prion diseases.

Sakudo A, Ikuta K.

Curr Med Chem. 2009;16(3):380-9. Review.

PMID:
19149584
16.

Squalestatin cures prion-infected neurons and protects against prion neurotoxicity.

Bate C, Salmona M, Diomede L, Williams A.

J Biol Chem. 2004 Apr 9;279(15):14983-90. Epub 2004 Jan 29.

17.

Altered glycosylated PrP proteins can have different neuronal trafficking in brain but do not acquire scrapie-like properties.

Cancellotti E, Wiseman F, Tuzi NL, Baybutt H, Monaghan P, Aitchison L, Simpson J, Manson JC.

J Biol Chem. 2005 Dec 30;280(52):42909-18. Epub 2005 Oct 11.

18.

Scrapie-specific neuronal lesions are independent of neuronal PrP expression.

Jeffrey M, Goodsir CM, Race RE, Chesebro B.

Ann Neurol. 2004 Jun;55(6):781-92.

PMID:
15174012
19.

Differential solubility of prions is associated in manifold phenotypes.

Kuczius T, Karch H, Groschup MH.

Mol Cell Neurosci. 2009 Nov;42(3):226-33. doi: 10.1016/j.mcn.2009.07.004. Epub 2009 Jul 14.

PMID:
19607920
20.

Prions can infect primary cultured neurons and astrocytes and promote neuronal cell death.

Cronier S, Laude H, Peyrin JM.

Proc Natl Acad Sci U S A. 2004 Aug 17;101(33):12271-6. Epub 2004 Aug 9.

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