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Results: 1 to 20 of 129

Similar articles for PubMed (Select 22876179)

1.

Small protease sensitive oligomers of PrPSc in distinct human prions determine conversion rate of PrP(C).

Kim C, Haldiman T, Surewicz K, Cohen Y, Chen W, Blevins J, Sy MS, Cohen M, Kong Q, Telling GC, Surewicz WK, Safar JG.

PLoS Pathog. 2012;8(8):e1002835. doi: 10.1371/journal.ppat.1002835. Epub 2012 Aug 2.

2.

Protease-sensitive conformers in broad spectrum of distinct PrPSc structures in sporadic Creutzfeldt-Jakob disease are indicator of progression rate.

Kim C, Haldiman T, Cohen Y, Chen W, Blevins J, Sy MS, Cohen M, Safar JG.

PLoS Pathog. 2011 Sep;7(9):e1002242. doi: 10.1371/journal.ppat.1002242. Epub 2011 Sep 8.

3.

Identification of distinct N-terminal truncated forms of prion protein in different Creutzfeldt-Jakob disease subtypes.

Zanusso G, Farinazzo A, Prelli F, Fiorini M, Gelati M, Ferrari S, Righetti PG, Rizzuto N, Frangione B, Monaco S.

J Biol Chem. 2004 Sep 10;279(37):38936-42. Epub 2004 Jul 9.

4.

Co-existence of distinct prion types enables conformational evolution of human PrPSc by competitive selection.

Haldiman T, Kim C, Cohen Y, Chen W, Blevins J, Qing L, Cohen ML, Langeveld J, Telling GC, Kong Q, Safar JG.

J Biol Chem. 2013 Oct 11;288(41):29846-61. doi: 10.1074/jbc.M113.500108. Epub 2013 Aug 23.

5.

Analyses of protease resistance and aggregation state of abnormal prion protein across the spectrum of human prions.

Saverioni D, Notari S, Capellari S, Poggiolini I, Giese A, Kretzschmar HA, Parchi P.

J Biol Chem. 2013 Sep 27;288(39):27972-85. doi: 10.1074/jbc.M113.477547. Epub 2013 Jul 29.

6.

pH-dependent prion protein conformation in classical Creutzfeldt-Jakob disease.

Zanusso G, Farinazzo A, Fiorini M, Gelati M, Castagna A, Righetti PG, Rizzuto N, Monaco S.

J Biol Chem. 2001 Nov 2;276(44):40377-80. Epub 2001 Sep 10.

7.

A traceback phenomenon can reveal the origin of prion infection.

Kobayashi A, Asano M, Mohri S, Kitamoto T.

Neuropathology. 2009 Oct;29(5):619-24. doi: 10.1111/j.1440-1789.2008.00973.x. Epub 2009 Jul 29.

PMID:
19659941
8.

Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics.

Cali I, Castellani R, Alshekhlee A, Cohen Y, Blevins J, Yuan J, Langeveld JP, Parchi P, Safar JG, Zou WQ, Gambetti P.

Brain. 2009 Oct;132(Pt 10):2643-58. doi: 10.1093/brain/awp196. Epub 2009 Sep 4.

9.

Classification of sporadic Creutzfeldt-Jakob disease revisited.

Cali I, Castellani R, Yuan J, Al-Shekhlee A, Cohen ML, Xiao X, Moleres FJ, Parchi P, Zou WQ, Gambetti P.

Brain. 2006 Sep;129(Pt 9):2266-77.

10.

A new method for the characterization of strain-specific conformational stability of protease-sensitive and protease-resistant PrP.

Pirisinu L, Di Bari M, Marcon S, Vaccari G, D'Agostino C, Fazzi P, Esposito E, Galeno R, Langeveld J, Agrimi U, Nonno R.

PLoS One. 2010 Sep 14;5(9):e12723. doi: 10.1371/journal.pone.0012723.

11.

Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes.

Faucheux BA, Morain E, Diouron V, Brandel JP, Salomon D, Sazdovitch V, Privat N, Laplanche JL, Hauw JJ, Haïk S.

Neuropathol Appl Neurobiol. 2011 Aug;37(5):500-12. doi: 10.1111/j.1365-2990.2011.01179.x.

PMID:
21450052
12.

Aberrant metal binding by prion protein in human prion disease.

Wong BS, Chen SG, Colucci M, Xie Z, Pan T, Liu T, Li R, Gambetti P, Sy MS, Brown DR.

J Neurochem. 2001 Sep;78(6):1400-8.

PMID:
11579148
13.

Development of oligomeric prion-protein aggregates in a mouse model of prion disease.

Sasaki K, Minaki H, Iwaki T.

J Pathol. 2009 Sep;219(1):123-30. doi: 10.1002/path.2576.

PMID:
19479969
14.

Quantitative traits of prion strains are enciphered in the conformation of the prion protein.

Safar J, Cohen FE, Prusiner SB.

Arch Virol Suppl. 2000;(16):227-35.

PMID:
11214926
15.

Two-dimensional mapping of three phenotype-associated isoforms of the prion protein in sporadic Creutzfeldt-Jakob disease.

Zanusso G, Righetti PG, Ferrari S, Terrin L, Farinazzo A, Cardone F, Pocchiari M, Rizzuto N, Monaco S.

Electrophoresis. 2002 Jan;23(2):347-55.

PMID:
11840543
16.

Early appearance but lagged accumulation of detergent-insoluble prion protein in the brains of mice inoculated with a mouse-adapted Creutzfeldt-Jakob disease agent.

Nakaoke R, Sakaguchi S, Atarashi R, Nishida N, Arima K, Shigematsu K, Katamine S.

Cell Mol Neurobiol. 2000 Dec;20(6):717-30.

PMID:
11100979
17.

Experimental verification of a traceback phenomenon in prion infection.

Kobayashi A, Sakuma N, Matsuura Y, Mohri S, Aguzzi A, Kitamoto T.

J Virol. 2010 Apr;84(7):3230-8. doi: 10.1128/JVI.02387-09. Epub 2010 Jan 20.

18.

Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: UK cases 1991-2002.

Head MW, Bunn TJ, Bishop MT, McLoughlin V, Lowrie S, McKimmie CS, Williams MC, McCardle L, MacKenzie J, Knight R, Will RG, Ironside JW.

Ann Neurol. 2004 Jun;55(6):851-9.

PMID:
15174020
19.

Acidic pH and detergents enhance in vitro conversion of human brain PrPC to a PrPSc-like form.

Zou WQ, Cashman NR.

J Biol Chem. 2002 Nov 15;277(46):43942-7. Epub 2002 Aug 2.

20.

Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD.

Pastore M, Chin SS, Bell KL, Dong Z, Yang Q, Yang L, Yuan J, Chen SG, Gambetti P, Zou WQ.

Am J Pathol. 2005 Dec;167(6):1729-38.

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