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Results: 1 to 20 of 74

Similar articles for PubMed (Select 24307901)

1.

Convergence of synapses, endosomes, and prions in the biology of neurodegenerative diseases.

Gouras GK.

Int J Cell Biol. 2013;2013:141083. doi: 10.1155/2013/141083. Epub 2013 Nov 7. Review.

2.

[Can prion-like propagation occur in neurodegenerative diseases?: in view of transmissible systemic amyloidosis].

Yoshida K, Higuchi K, Ikeda S.

Brain Nerve. 2012 Jun;64(6):665-74. Review. Japanese.

PMID:
22647474
3.

The cell biology of prion-like spread of protein aggregates: mechanisms and implication in neurodegeneration.

Costanzo M, Zurzolo C.

Biochem J. 2013 May 15;452(1):1-17. doi: 10.1042/BJ20121898. Review.

PMID:
23614720
4.

Cellular mechanisms of protein aggregate propagation.

Holmes BB, Diamond MI.

Curr Opin Neurol. 2012 Dec;25(6):721-6. doi: 10.1097/WCO.0b013e32835a3ee0. Review.

5.

Prion-like mechanisms in neurodegenerative diseases.

Frost B, Diamond MI.

Nat Rev Neurosci. 2010 Mar;11(3):155-9. doi: 10.1038/nrn2786. Epub 2009 Dec 23. Review.

6.

Protein aggregation and degradation mechanisms in neurodegenerative diseases.

Takalo M, Salminen A, Soininen H, Hiltunen M, Haapasalo A.

Am J Neurodegener Dis. 2013;2(1):1-14. Epub 2013 Mar 8.

7.

The role of crowded physiological environments in prion and prion-like protein aggregation.

Ma Q, Hu JY, Chen J, Liang Y.

Int J Mol Sci. 2013 Oct 25;14(11):21339-52. doi: 10.3390/ijms141121339. Review.

8.

Prion protein misfolding, strains, and neurotoxicity: an update from studies on Mammalian prions.

Poggiolini I, Saverioni D, Parchi P.

Int J Cell Biol. 2013;2013:910314. doi: 10.1155/2013/910314. Epub 2013 Dec 24. Review.

9.

Nanoimaging for prion related diseases.

Krasnoslobodtsev AV, Portillo AM, Deckert-Gaudig T, Deckert V, Lyubchenko YL.

Prion. 2010 Oct-Dec;4(4):265-74. doi: 10.4161/pri.4.4.13125. Epub 2010 Oct 23. Review.

10.

Protein misfolding and neurodegeneration.

Soto C, Estrada LD.

Arch Neurol. 2008 Feb;65(2):184-9. doi: 10.1001/archneurol.2007.56. Review.

PMID:
18268186
11.

Generalization of the prion hypothesis to other neurodegenerative diseases: an imperfect fit.

Guest WC, Silverman JM, Pokrishevsky E, O'Neill MA, Grad LI, Cashman NR.

J Toxicol Environ Health A. 2011;74(22-24):1433-59. doi: 10.1080/15287394.2011.618967. Review.

PMID:
22043906
12.

Molecular pathogenesis of sporadic prion diseases in man.

Safar JG.

Prion. 2012 Apr-Jun;6(2):108-15. doi: 10.4161/pri.18666. Epub 2012 Apr 1. Review.

13.

Pathogenesis of prion diseases.

Unterberger U, Voigtländer T, Budka H.

Acta Neuropathol. 2005 Jan;109(1):32-48. Epub 2005 Jan 12. Review.

PMID:
15645262
14.

The role of chaperones in Parkinson's disease and prion diseases.

Winklhofer KF, Tatzelt J.

Handb Exp Pharmacol. 2006;(172):221-58. Review.

PMID:
16610362
15.

Oxidative stress and protein aggregation during biological aging.

Squier TC.

Exp Gerontol. 2001 Sep;36(9):1539-50. Review.

PMID:
11525876
16.

Recent progress in prion and prion-like protein aggregation.

Yi CW, Xu WC, Chen J, Liang Y.

Acta Biochim Biophys Sin (Shanghai). 2013 Jun;45(6):520-6. doi: 10.1093/abbs/gmt052. Review.

PMID:
23709368
17.

Role of metal ions in aggregation of intrinsically disordered proteins in neurodegenerative diseases.

Breydo L, Uversky VN.

Metallomics. 2011 Nov;3(11):1163-80. doi: 10.1039/c1mt00106j. Epub 2011 Aug 25. Review.

PMID:
21869995
18.

Prions: disease propagation and disease therapy by conformational transmission.

Soto C, Saborío GP.

Trends Mol Med. 2001 Mar;7(3):109-14. Review.

PMID:
11286781
19.

Structure and function of the molecular chaperone Hsp104 from yeast.

Grimminger-Marquardt V, Lashuel HA.

Biopolymers. 2010 Mar;93(3):252-76. doi: 10.1002/bip.21301. Review.

PMID:
19768774
20.

Cell-to-cell transmission of non-prion protein aggregates.

Lee SJ, Desplats P, Sigurdson C, Tsigelny I, Masliah E.

Nat Rev Neurol. 2010 Dec;6(12):702-6. doi: 10.1038/nrneurol.2010.145. Epub 2010 Oct 12. Erratum in: Nat Rev Neurol. 2011 Jan;7(1):5.

PMID:
21045796
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