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Results: 1 to 20 of 127

Similar articles for PubMed (Select 7909169)

1.

Structural clues to prion replication.

Cohen FE, Pan KM, Huang Z, Baldwin M, Fletterick RJ, Prusiner SB.

Science. 1994 Apr 22;264(5158):530-1. No abstract available.

PMID:
7909169
2.

Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity.

Telling GC, Parchi P, DeArmond SJ, Cortelli P, Montagna P, Gabizon R, Mastrianni J, Lugaresi E, Gambetti P, Prusiner SB.

Science. 1996 Dec 20;274(5295):2079-82.

PMID:
8953038
3.

A transmembrane form of the prion protein in neurodegenerative disease.

Hegde RS, Mastrianni JA, Scott MR, DeFea KA, Tremblay P, Torchia M, DeArmond SJ, Prusiner SB, Lingappa VR.

Science. 1998 Feb 6;279(5352):827-34.

4.

Prion protein interconversions and the transmissible spongiform encephalopathies.

Horiuchi M, Caughey B.

Structure. 1999 Oct 15;7(10):R231-40. Review.

PMID:
10545332
5.

Transmissible spongiform encephalopathies: prion proof in progress.

Edskes HK, Wickner RB.

Nature. 2004 Aug 26;430(7003):977-9. No abstract available.

PMID:
15329705
6.

Deadly conformations--protein misfolding in prion disease.

Horwich AL, Weissman JS.

Cell. 1997 May 16;89(4):499-510. Review. No abstract available.

7.

Transmissible spongiform encephalopathies and prion protein interconversions.

Caughey B, Chesebro B.

Adv Virus Res. 2001;56:277-311. Review. No abstract available.

PMID:
11450303
8.

Molecular biology and pathogenesis of prion diseases.

Prusiner SB.

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

PMID:
9009832
9.

Prion propagation and molecular chaperones.

Zahn R.

Q Rev Biophys. 1999 Nov;32(4):309-70. Review. No abstract available.

PMID:
11194568
10.

Genetic and infectious prion diseases.

Prusiner SB.

Arch Neurol. 1993 Nov;50(11):1129-53. Review.

PMID:
8105771
11.

Spongiform encephalopathies. Tracking turncoat prion proteins.

Masters CL, Beyreuther K.

Nature. 1997 Jul 17;388(6639):228-9. No abstract available.

PMID:
9230425
12.

The reconstitution of mammalian prion infectivity de novo.

Baskakov IV.

FEBS J. 2007 Feb;274(3):576-87. Review.

PMID:
17288547
13.

Transgenetic investigations of prion diseases of humans and animals.

Prusiner SB.

Philos Trans R Soc Lond B Biol Sci. 1993 Feb 27;339(1288):239-54. Review.

PMID:
8097053
14.

Anchorless prion protein results in infectious amyloid disease without clinical scrapie.

Chesebro B, Trifilo M, Race R, Meade-White K, Teng C, LaCasse R, Raymond L, Favara C, Baron G, Priola S, Caughey B, Masliah E, Oldstone M.

Science. 2005 Jun 3;308(5727):1435-9.

15.

Molecular biology and genetics of prion diseases.

Prusiner SB.

Philos Trans R Soc Lond B Biol Sci. 1994 Mar 29;343(1306):447-63. Review.

PMID:
7913765
16.

Species barriers in a model for specific prion protein dimerisation.

Warwicker J.

Biochem Biophys Res Commun. 1997 Mar 17;232(2):508-12.

PMID:
9125211
17.

Ironing out the wrinkles in the prion strain problem.

Grady D.

Science. 1996 Dec 20;274(5295):2010. No abstract available.

PMID:
8984659
18.

Molecular genetics and biophysics of prions.

Prusiner SB.

Uirusu. 1995 Jun;45(1):5-42. Review. No abstract available.

19.
20.

Familial prion disease mutation alters the secondary structure of recombinant mouse prion protein: implications for the mechanism of prion formation.

Cappai R, Stewart L, Jobling MF, Thyer JM, White AR, Beyreuther K, Collins SJ, Masters CL, Barrow CJ.

Biochemistry. 1999 Mar 16;38(11):3280-4.

PMID:
10079070
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