Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 30

1.
2.

Insights into intragenic and extragenic effectors of prion propagation using chimeric prion proteins.

True HL, Kalastavadi T, Tank EM.

Prion. 2008 Apr-Jun;2(2):45-7. Epub 2008 Apr 17. Review.

3.

[Mechanism and application of molecular self-assembly in Sup35 prion domain of Saccharomyces cerevisiae].

Yin W, He J, Yu Z, Wang J.

Sheng Wu Gong Cheng Xue Bao. 2011 Oct;27(10):1401-7. Review. Chinese.

PMID:
22260056
4.

Ligand binding and hydration in protein misfolding: insights from studies of prion and p53 tumor suppressor proteins.

Silva JL, Vieira TC, Gomes MP, Bom AP, Lima LM, Freitas MS, Ishimaru D, Cordeiro Y, Foguel D.

Acc Chem Res. 2010 Feb 16;43(2):271-9. doi: 10.1021/ar900179t. Review.

5.

Probing the role of structural features of mouse PrP in yeast by expression as Sup35-PrP fusions.

Jossé L, Marchante R, Zenthon J, von der Haar T, Tuite MF.

Prion. 2012 Jul 1;6(3):201-10. doi: 10.4161/pri.19214. Epub 2012 Jul 1. Review.

6.

Prion amyloid structure explains templating: how proteins can be genes.

Wickner RB, Shewmaker F, Edskes H, Kryndushkin D, Nemecek J, McGlinchey R, Bateman D, Winchester CL.

FEMS Yeast Res. 2010 Dec;10(8):980-91. doi: 10.1111/j.1567-1364.2010.00666.x. Review.

7.

Prion protein misfolding and disease.

Moore RA, Taubner LM, Priola SA.

Curr Opin Struct Biol. 2009 Feb;19(1):14-22. doi: 10.1016/j.sbi.2008.12.007. Epub 2009 Jan 20. Review.

8.

Amyloids, prions and the inherent infectious nature of misfolded protein aggregates.

Soto C, Estrada L, Castilla J.

Trends Biochem Sci. 2006 Mar;31(3):150-5. Epub 2006 Feb 13. Review.

PMID:
16473510
9.

Self-perpetuating changes in Sup35 protein conformation as a mechanism of heredity in yeast.

Serio TR, Cashikar AG, Kowal AS, Sawicki GJ, Lindquist SL.

Biochem Soc Symp. 2001;(68):35-43. Review.

PMID:
11573346
10.

Life cycle of yeast prions: propagation mediated by amyloid fibrils.

Inoue Y.

Protein Pept Lett. 2009;16(3):271-6. Review.

PMID:
19275740
11.

Prion and nonprion amyloids: a comparison inspired by the yeast Sup35 protein.

Kushnirov VV, Vishnevskaya AB, Alexandrov IM, Ter-Avanesyan MD.

Prion. 2007 Jul-Sep;1(3):179-84. Epub 2007 Jul 6. Review.

12.

Amyloid formation of a yeast prion determinant.

Scheibel T.

J Mol Neurosci. 2004;23(1-2):13-22. Review.

PMID:
15126688
13.

Prion-like aggregates: infectious agents in human disease.

Westermark GT, Westermark P.

Trends Mol Med. 2010 Nov;16(11):501-7. doi: 10.1016/j.molmed.2010.08.004. Epub 2010 Oct 1. Review.

PMID:
20870462
14.

The utility of prions.

Osherovich LZ, Weissman JS.

Dev Cell. 2002 Feb;2(2):143-51. Review.

15.

A bipolar personality of yeast prion proteins.

Kurahashi H, Oishi K, Nakamura Y.

Prion. 2011 Oct-Dec;5(4):305-10. doi: 10.4161/pri.18307. Epub 2011 Oct 1. Review.

16.

[Yeast prions, mammalian amyloidoses, and the problem of proteomic networks].

Galkin AP, Mironova LN, Zhuravleva GA, Inge-Vechtomov SG.

Genetika. 2006 Nov;42(11):1558-70. Review. Russian.

PMID:
17163073
17.

Misfolded protein aggregates: mechanisms, structures and potential for disease transmission.

Moreno-Gonzalez I, Soto C.

Semin Cell Dev Biol. 2011 Jul;22(5):482-7. doi: 10.1016/j.semcdb.2011.04.002. Epub 2011 May 5. Review.

18.

Amyloid oligomers: diffuse oligomer-based transmission of yeast prions.

Taguchi H, Kawai-Noma S.

FEBS J. 2010 Mar;277(6):1359-68. doi: 10.1111/j.1742-4658.2010.07569.x. Epub 2010 Feb 9. Review.

19.

Interactions between non-identical prion proteins.

Gonzalez Nelson AC, Ross ED.

Semin Cell Dev Biol. 2011 Jul;22(5):437-43. doi: 10.1016/j.semcdb.2011.02.022. Epub 2011 Feb 24. Review.

PMID:
21354317
20.

[Neurodegenerative amyloidoses: the yeast model].

Vishnevskaia AB, Kushnirov VV, Ter-Avanesian MD.

Mol Biol (Mosk). 2007 Mar-Apr;41(2):346-54. Review. Russian.

PMID:
17514901

Supplemental Content

Support Center