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Items: 16

1.

Prion-forming ability of Ure2 of yeasts is not evolutionarily conserved.

Edskes HK, Engel A, McCann LM, Brachmann A, Tsai HF, Wickner RB.

Genetics. 2011 May;188(1):81-90. doi: 10.1534/genetics.111.127217. Epub 2011 Mar 2.

2.

Prions in Saccharomyces and Podospora spp.: protein-based inheritance.

Wickner RB, Taylor KL, Edskes HK, Maddelein ML, Moriyama H, Roberts BT.

Microbiol Mol Biol Rev. 1999 Dec;63(4):844-61, table of contents. Review.

3.

Prions of yeast as heritable amyloidoses.

Wickner RB, Taylor KL, Edskes HK, Maddelein ML, Moriyama H, Roberts BT.

J Struct Biol. 2000 Jun;130(2-3):310-22. Review.

PMID:
10940235
4.

Prions of yeast as epigenetic phenomena: high protein "copy number" inducing protein "silencing".

Wickner RB, Edskes HK, Roberts BT, Pierce M, Baxa U.

Adv Genet. 2002;46:485-525. Review.

PMID:
11931236
5.

The [URE3] yeast prion: from genetics to biochemistry.

Komar AA, Melki R, Cullin C.

Biochemistry (Mosc). 1999 Dec;64(12):1401-7. Review.

6.

Prion model in yeast.

Sapriel G.

Res Microbiol. 2001 Jul-Aug;152(6):531-8. Review.

PMID:
11501671
7.
8.

Structure, function, and amyloidogenesis of fungal prions: filament polymorphism and prion variants.

Baxa U, Cassese T, Kajava AV, Steven AC.

Adv Protein Chem. 2006;73:125-80. Review.

PMID:
17190613
9.

Yeast prions assembly and propagation: contributions of the prion and non-prion moieties and the nature of assemblies.

Kabani M, Melki R.

Prion. 2011 Oct-Dec;5(4):277-84. doi: 10.4161/pri.18070. Epub 2011 Oct 1. Review.

10.

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.

11.

Yeast prions: evolution of the prion concept.

Wickner RB, Edskes HK, Shewmaker F, Nakayashiki T, Engel A, McCann L, Kryndushkin D.

Prion. 2007 Apr-Jun;1(2):94-100. Epub 2007 Apr 28. Review.

12.

The yeast prion protein Ure2: insights into the mechanism of amyloid formation.

Chen LJ, Sawyer EB, Perrett S.

Biochem Soc Trans. 2011 Oct;39(5):1359-64. doi: 10.1042/BST0391359. Review.

PMID:
21936815
13.

Prion diseases of yeast: amyloid structure and biology.

Wickner RB, Edskes HK, Kryndushkin D, McGlinchey R, Bateman D, Kelly A.

Semin Cell Dev Biol. 2011 Jul;22(5):469-75. doi: 10.1016/j.semcdb.2011.02.021. Epub 2011 Feb 21. Review.

14.

The yeast prions [PSI+] and [URE3] are molecular degenerative diseases.

Wickner RB, Edskes HK, Bateman D, Kelly AC, Gorkovskiy A.

Prion. 2011 Oct-Dec;5(4):258-62. doi: 10.4161/pri.17748. Epub 2011 Oct 1. Review.

15.

[Structure and functional similarity of yeast Sup35p and Ure2p proteins to mammalian prions].

Kushnirov VV, Ter-Avanesian MD, Smirnov VN.

Mol Biol (Mosk). 1995 Jul-Aug;29(4):750-5. Review. Russian.

PMID:
7476941
16.

As a toxin dies a prion comes to life: A tentative natural history of the [Het-s] prion.

Daskalov A, Saupe SJ.

Prion. 2015;9(3):184-9. doi: 10.1080/19336896.2015.1038018. Review.

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