Similar articles for PMID: 26061765

Year	Number of Results
1968	1
1991	1
1993	2
1994	2
1995	2
1996	4
1997	8
1998	3
1999	4
2000	1
2001	6
2002	4
2003	6
2004	4
2006	9
2007	5
2008	6
2009	11
2010	4
2011	6
2012	8
2013	8
2014	12
2015	5
2016	6
2017	8
2018	6
2019	6
2020	8
2021	8
2022	30
2023	13
2024	1

1

A naturally occurring variant of the human prion protein completely prevents prion disease.

Asante EA, Smidak M, Grimshaw A, Houghton R, Tomlinson A, Jeelani A, Jakubcova T, Hamdan S, Richard-Londt A, Linehan JM, Brandner S, Alpers M, Whitfield J, Mead S, Wadsworth JD, Collinge J. Asante EA, et al. Nature. 2015 Jun 25;522(7557):478-81. doi: 10.1038/nature14510. Epub 2015 Jun 10. Nature. 2015. PMID: 26061765 Free PMC article.

2

Human prion protein (PrP) 219K is converted to PrPSc but shows heterozygous inhibition in variant Creutzfeldt-Jakob disease infection.

Hizume M, Kobayashi A, Teruya K, Ohashi H, Ironside JW, Mohri S, Kitamoto T. Hizume M, et al. J Biol Chem. 2009 Feb 6;284(6):3603-9. doi: 10.1074/jbc.M809254200. Epub 2008 Dec 10. J Biol Chem. 2009. PMID: 19074151 Free article.

3

Genetic and infectious prion diseases.

Prusiner SB. Prusiner SB. Arch Neurol. 1993 Nov;50(11):1129-53. doi: 10.1001/archneur.1993.00540110011002. Arch Neurol. 1993. PMID: 8105771 Review.

4

Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.

Mead S, Uphill J, Beck J, Poulter M, Campbell T, Lowe J, Adamson G, Hummerich H, Klopp N, Rückert IM, Wichmann HE, Azazi D, Plagnol V, Pako WH, Whitfield J, Alpers MP, Whittaker J, Balding DJ, Zerr I, Kretzschmar H, Collinge J. Mead S, et al. Hum Mol Genet. 2012 Apr 15;21(8):1897-906. doi: 10.1093/hmg/ddr607. Epub 2011 Dec 30. Hum Mol Genet. 2012. PMID: 22210626 Free PMC article.

5

Absence of Evidence for a Causal Link between Bovine Spongiform Encephalopathy Strain Variant L-BSE and Known Forms of Sporadic Creutzfeldt-Jakob Disease in Human PrP Transgenic Mice.

Jaumain E, Quadrio I, Herzog L, Reine F, Rezaei H, Andréoletti O, Laude H, Perret-Liaudet A, Haïk S, Béringue V. Jaumain E, et al. J Virol. 2016 Nov 14;90(23):10867-10874. doi: 10.1128/JVI.01383-16. Print 2016 Dec 1. J Virol. 2016. PMID: 27681129 Free PMC article.

6

Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice.

Wadsworth JD, Joiner S, Linehan JM, Desbruslais M, Fox K, Cooper S, Cronier S, Asante EA, Mead S, Brandner S, Hill AF, Collinge J. Wadsworth JD, et al. Proc Natl Acad Sci U S A. 2008 Mar 11;105(10):3885-90. doi: 10.1073/pnas.0800190105. Epub 2008 Mar 3. Proc Natl Acad Sci U S A. 2008. PMID: 18316717 Free PMC article.

7

Review. The origin of the prion agent of kuru: molecular and biological strain typing.

Wadsworth JD, Joiner S, Linehan JM, Asante EA, Brandner S, Collinge J. Wadsworth JD, et al. Philos Trans R Soc Lond B Biol Sci. 2008 Nov 27;363(1510):3747-53. doi: 10.1098/rstb.2008.0069. Philos Trans R Soc Lond B Biol Sci. 2008. PMID: 18849291 Free PMC article. Review.

8

Human prion diseases: from Kuru to variant Creutzfeldt-Jakob disease.

Sikorska B, Liberski PP. Sikorska B, et al. Subcell Biochem. 2012;65:457-96. doi: 10.1007/978-94-007-5416-4_17. Subcell Biochem. 2012. PMID: 23225013 Review.

9

An overview of human prion diseases.

Imran M, Mahmood S. Imran M, et al. Virol J. 2011 Dec 24;8:559. doi: 10.1186/1743-422X-8-559. Virol J. 2011. PMID: 22196171 Free PMC article. Review.

10

Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins.

Asante EA, Gowland I, Grimshaw A, Linehan JM, Smidak M, Houghton R, Osiguwa O, Tomlinson A, Joiner S, Brandner S, Wadsworth JDF, Collinge J. Asante EA, et al. J Gen Virol. 2009 Mar;90(Pt 3):546-558. doi: 10.1099/vir.0.007930-0. J Gen Virol. 2009. PMID: 19218199 Free PMC article.

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