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Items: 1 to 20 of 79

1.

Kuru in the 21st century--an acquired human prion disease with very long incubation periods.

Collinge J, Whitfield J, McKintosh E, Beck J, Mead S, Thomas DJ, Alpers MP.

Lancet. 2006 Jun 24;367(9528):2068-74.

PMID:
16798390
2.

Risk factors for variant Creutzfeldt-Jakob disease: a case-control study.

Ward HJ, Everington D, Cousens SN, Smith-Bathgate B, Leitch M, Cooper S, Heath C, Knight RS, Smith PG, Will RG.

Ann Neurol. 2006 Jan;59(1):111-20.

PMID:
16287153
3.

Creutzfeldt-Jakob disease: Australian surveillance update to 31 December 2004.

Klug GM, Boyd A, Lewis V, Kvasnicka M, Lee JS, Masters CL, Collins SJ.

Commun Dis Intell Q Rep. 2005;29(3):269-71. Review.

4.

Selective precipitation of prions by polyoxometalate complexes.

Lee IS, Long JR, Prusiner SB, Safar JG.

J Am Chem Soc. 2005 Oct 12;127(40):13802-3.

PMID:
16201796
5.

Prion generation in vitro: amyloid of Ure2p is infectious.

Brachmann A, Baxa U, Wickner RB.

EMBO J. 2005 Sep 7;24(17):3082-92. Epub 2005 Aug 11.

7.

Search for a prion-specific nucleic acid.

Safar JG, Kellings K, Serban A, Groth D, Cleaver JE, Prusiner SB, Riesner D.

J Virol. 2005 Aug;79(16):10796-806.

8.

Australian sporadic CJD analysis supports endogenous determinants of molecular-clinical profiles.

Lewis V, Hill AF, Klug GM, Boyd A, Masters CL, Collins SJ.

Neurology. 2005 Jul 12;65(1):113-8.

PMID:
16009895
9.

Transmission barriers for bovine, ovine, and human prions in transgenic mice.

Scott MR, Peretz D, Nguyen HO, Dearmond SJ, Prusiner SB.

J Virol. 2005 May;79(9):5259-71.

10.

Diagnosis of human prion disease.

Safar JG, Geschwind MD, Deering C, Didorenko S, Sattavat M, Sanchez H, Serban A, Vey M, Baron H, Giles K, Miller BL, Dearmond SJ, Prusiner SB.

Proc Natl Acad Sci U S A. 2005 Mar 1;102(9):3501-6.

11.

Strain-specified characteristics of mouse synthetic prions.

Legname G, Nguyen HO, Baskakov IV, Cohen FE, Dearmond SJ, Prusiner SB.

Proc Natl Acad Sci U S A. 2005 Feb 8;102(6):2168-73. Epub 2005 Jan 25. Erratum in: Proc Natl Acad Sci U S A. 2006 Sep 26;103(39):14642.

12.

Biomedicine. A fresh look at BSE.

Chesebro B.

Science. 2004 Sep 24;305(5692):1918-21. No abstract available.

PMID:
15448258
13.

Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient.

Peden AH, Head MW, Ritchie DL, Bell JE, Ironside JW.

Lancet. 2004 Aug 7-13;364(9433):527-9.

PMID:
15302196
14.

Synthetic mammalian prions.

Legname G, Baskakov IV, Nguyen HO, Riesner D, Cohen FE, DeArmond SJ, Prusiner SB.

Science. 2004 Jul 30;305(5684):673-6.

15.

Detecting mad cow disease.

Prusiner SB.

Sci Am. 2004 Jul;291(1):86-93. No abstract available.

PMID:
15255592
16.

Prevalence of lymphoreticular prion protein accumulation in UK tissue samples.

Hilton DA, Ghani AC, Conyers L, Edwards P, McCardle L, Ritchie D, Penney M, Hegazy D, Ironside JW.

J Pathol. 2004 Jul;203(3):733-9.

PMID:
15221931
17.

Standards for the assay of Creutzfeldt-Jakob disease specimens.

Minor P, Newham J, Jones N, Bergeron C, Gregori L, Asher D, van Engelenburg F, Stroebel T, Vey M, Barnard G, Head M; WHO Working Group on International Reference Materials for the Diagnosis and Study of Transmissible Spongiform Encephalopathies.

J Gen Virol. 2004 Jun;85(Pt 6):1777-84.

PMID:
15166463
18.

PrPSc accumulation in myocytes from sheep incubating natural scrapie.

Andréoletti O, Simon S, Lacroux C, Morel N, Tabouret G, Chabert A, Lugan S, Corbière F, Ferré P, Foucras G, Laude H, Eychenne F, Grassi J, Schelcher F.

Nat Med. 2004 Jun;10(6):591-3. Epub 2004 May 23.

PMID:
15156203
19.

Conformational variations in an infectious protein determine prion strain differences.

Tanaka M, Chien P, Naber N, Cooke R, Weissman JS.

Nature. 2004 Mar 18;428(6980):323-8.

20.

Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion.

Llewelyn CA, Hewitt PE, Knight RS, Amar K, Cousens S, Mackenzie J, Will RG.

Lancet. 2004 Feb 7;363(9407):417-21.

PMID:
14962520

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