Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 27

1.

A novel human disease with abnormal prion protein sensitive to protease.

Gambetti P, Dong Z, Yuan J, Xiao X, Zheng M, Alshekhlee A, Castellani R, Cohen M, Barria MA, Gonzalez-Romero D, Belay ED, Schonberger LB, Marder K, Harris C, Burke JR, Montine T, Wisniewski T, Dickson DW, Soto C, Hulette CM, Mastrianni JA, Kong Q, Zou WQ.

Ann Neurol. 2008 Jun;63(6):697-708. doi: 10.1002/ana.21420.

2.

Variably protease-sensitive prionopathy in the UK: a retrospective review 1991-2008.

Head MW, Yull HM, Ritchie DL, Langeveld JP, Fletcher NA, Knight RS, Ironside JW.

Brain. 2013 Apr;136(Pt 4):1102-15. doi: 10.1093/brain/aws366. Review. Erratum in: Brain. 2013 Nov;136(Pt 11):i1.

PMID:
23550113
3.

Contribution of neuropathology to the understanding of human prion disease.

Kovács GG, Kalev O, Budka H.

Folia Neuropathol. 2004;42 Suppl A:69-76. Review.

PMID:
15449461
4.

Molecular pathology of human prion diseases.

Kovacs GG, Budka H.

Int J Mol Sci. 2009 Mar;10(3):976-99. doi: 10.3390/ijms10030976. Epub 2009 Mar 9. Review.

5.

Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia.

Parchi P, Capellari S, Gambetti P.

Microsc Res Tech. 2000 Jul 1;50(1):16-25. Review.

PMID:
10871544
6.

Prion protein amyloidosis.

Ghetti B, Piccardo P, Frangione B, Bugiani O, Giaccone G, Young K, Prelli F, Farlow MR, Dlouhy SR, Tagliavini F.

Brain Pathol. 1996 Apr;6(2):127-45. Review.

PMID:
8737929
7.

A transgenic model of a familial prion disease.

Harris DA, Chiesa R, Drisaldi B, Quaglio E, Migheli A, Piccardo P, Ghetti B.

Arch Virol Suppl. 2000;(16):103-12. Review.

PMID:
11214912
8.

Proteomic analysis of prion diseases: creating clarity or causing confusion?

Rubenstein R.

Electrophoresis. 2012 Dec;33(24):3631-43. doi: 10.1002/elps.201200310. Epub 2012 Nov 23. Review.

PMID:
23161058
9.

Fundamentals of prion biology and diseases.

DeArmond SJ, Bouzamondo E.

Toxicology. 2002 Dec 27;181-182:9-16. Review.

PMID:
12505278
10.

Neuropathology and molecular biology of variant Creutzfeldt-Jakob disease.

Ironside JW, Head MW.

Curr Top Microbiol Immunol. 2004;284:133-59. Review.

PMID:
15148991
11.

Cellular and sub-cellular pathology of animal prion diseases: relationship between morphological changes, accumulation of abnormal prion protein and clinical disease.

Jeffrey M, McGovern G, Sisó S, González L.

Acta Neuropathol. 2011 Jan;121(1):113-34. doi: 10.1007/s00401-010-0700-3. Epub 2010 Jun 8. Review.

PMID:
20532540
12.

Prion protein transgenes and the neuropathology in prion diseases.

DeArmond SJ, Prusiner SB.

Brain Pathol. 1995 Jan;5(1):77-89. Review.

PMID:
7767493
13.

Formation of protease-resistant prion protein in cell-free systems.

Caughey B.

Curr Issues Mol Biol. 2000 Jul;2(3):95-101. Review.

14.

A hypothesis on prion disorders: are infectious, inherited, and sporadic causes so distinct?

Fornai F, Ferrucci M, Gesi M, Bandettini di Poggio A, Giorgi FS, Biagioni F, Paparelli A.

Brain Res Bull. 2006 Mar 31;69(2):95-100. Epub 2006 Jan 4. Review.

PMID:
16533656
15.
16.

Molecular mechanisms of neurotoxicity of pathological prion protein.

Castilla J, Hetz C, Soto C.

Curr Mol Med. 2004 Jun;4(4):397-403. Review.

PMID:
15354870
17.

The role of PrP in health and disease.

Flechsig E, Weissmann C.

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

PMID:
15354865
18.

Understanding the natural variability of prion diseases.

Geissen M, Krasemann S, Matschke J, Glatzel M.

Vaccine. 2007 Jul 26;25(30):5631-6. Epub 2007 Mar 7. Review.

PMID:
17391814
19.

Molecular biology and pathogenesis of prion diseases.

Prusiner SB.

Trends Biochem Sci. 1996 Dec;21(12):482-7. Review.

PMID:
9009832
20.

Prions in variably protease-sensitive prionopathy: an update.

Zou WQ, Gambetti P, Xiao X, Yuan J, Langeveld J, Pirisinu L.

Pathogens. 2013 Jul 5;2(3):457-71. doi: 10.3390/pathogens2030457. Review.

Supplemental Content

Support Center