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Results: 1 to 20 of 209

Similar articles for PubMed (Select 16452616)

1.

Octapeptide repeat insertions increase the rate of protease-resistant prion protein formation.

Moore RA, Herzog C, Errett J, Kocisko DA, Arnold KM, Hayes SF, Priola SA.

Protein Sci. 2006 Mar;15(3):609-19. Epub 2006 Feb 1.

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4.

N-terminal truncation of prion protein affects both formation and conformation of abnormal protease-resistant prion protein generated in vitro.

Lawson VA, Priola SA, Wehrly K, Chesebro B.

J Biol Chem. 2001 Sep 21;276(38):35265-71. Epub 2001 Jul 20.

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6.

Inhibition of interactions and interconversions of prion protein isoforms by peptide fragments from the C-terminal folded domain.

Horiuchi M, Baron GS, Xiong LW, Caughey B.

J Biol Chem. 2001 May 4;276(18):15489-97. Epub 2001 Feb 1.

7.

Factors affecting interactions between prion protein isoforms.

Caughey B, Baron GS.

Biochem Soc Trans. 2002 Aug;30(4):565-9.

PMID:
12196138
8.

The spectrum of transmissible spongiform encephalopathies.

Weber T, Aguzzi A.

Intervirology. 1997;40(2-3):198-212. Review.

PMID:
9450236
10.

Prion protein insertional mutations increase aggregation propensity but not fiber stability.

Kalastavadi T, True HL.

BMC Biochem. 2008 Mar 17;9:7. doi: 10.1186/1471-2091-9-7.

11.

Rapidly progressive dementia syndrome associated with a novel four extra repeat mutation in the prion protein gene.

Yanagihara C, Yasuda M, Maeda K, Miyoshi K, Nishimura Y.

J Neurol Neurosurg Psychiatry. 2002 Jun;72(6):788-91.

12.

Prion protein and species barriers in the transmissible spongiform encephalopathies.

Priola SA.

Biomed Pharmacother. 1999;53(1):27-33. Review.

PMID:
10221165
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.

Different behavior toward bovine spongiform encephalopathy infection of bovine prion protein transgenic mice with one extra repeat octapeptide insert mutation.

Castilla J, Gutiérrez-Adán A, Brun A, Pintado B, Parra B, Ramírez MA, Salguero FJ, Díaz San Segundo F, Rábano A, Cano MJ, Torres JM.

J Neurosci. 2004 Mar 3;24(9):2156-64.

15.

Creutzfeldt-Jakob disease with a novel four extra-repeat insertional mutation in the PrP gene.

Rossi G, Giaccone G, Giampaolo L, Iussich S, Puoti G, Frigo M, Cavaletti G, Frattola L, Bugiani O, Tagliavini F.

Neurology. 2000 Aug 8;55(3):405-10.

PMID:
10932276
16.

Conformational change, aggregation and fibril formation induced by detergent treatments of cellular prion protein.

Xiong LW, Raymond LD, Hayes SF, Raymond GJ, Caughey B.

J Neurochem. 2001 Nov;79(3):669-78.

PMID:
11701770
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18.

Multiple amino acid residues within the rabbit prion protein inhibit formation of its abnormal isoform.

Vorberg I, Groschup MH, Pfaff E, Priola SA.

J Virol. 2003 Feb;77(3):2003-9.

20.

Early onset prion disease from octarepeat expansion correlates with copper binding properties.

Stevens DJ, Walter ED, Rodríguez A, Draper D, Davies P, Brown DR, Millhauser GL.

PLoS Pathog. 2009 Apr;5(4):e1000390. doi: 10.1371/journal.ppat.1000390. Epub 2009 Apr 17.

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