Similar articles for PMID: 8953038

Year	Number of Results
1990	1
1991	3
1992	4
1993	6
1994	6
1995	5
1996	12
1997	9
1998	11
1999	18
2000	12
2001	13
2002	11
2003	20
2004	12
2005	10
2006	9
2007	9
2008	8
2009	10
2010	11
2011	10
2012	8
2013	11
2014	10
2015	3
2016	6
2017	8
2018	5
2019	12
2020	10
2021	9
2022	3
2023	1
2024	0

1

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. Telling GC, et al. Science. 1996 Dec 20;274(5295):2079-82. doi: 10.1126/science.274.5295.2079. Science. 1996. PMID: 8953038

2

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.

3

Towards authentic transgenic mouse models of heritable PrP prion diseases.

Watts JC, Giles K, Bourkas ME, Patel S, Oehler A, Gavidia M, Bhardwaj S, Lee J, Prusiner SB. Watts JC, et al. Acta Neuropathol. 2016 Oct;132(4):593-610. doi: 10.1007/s00401-016-1585-6. Epub 2016 Jun 28. Acta Neuropathol. 2016. PMID: 27350609 Free PMC article.

4

Prion protein transgenes and the neuropathology in prion diseases.

DeArmond SJ, Prusiner SB. DeArmond SJ, et al. Brain Pathol. 1995 Jan;5(1):77-89. doi: 10.1111/j.1750-3639.1995.tb00579.x. Brain Pathol. 1995. PMID: 7767493 Review.

5

Prion encephalopathies of animals and humans.

Prusiner SB. Prusiner SB. Dev Biol Stand. 1993;80:31-44. Dev Biol Stand. 1993. PMID: 8270114 Review.

6

Synthetic mammalian prions.

Legname G, Baskakov IV, Nguyen HO, Riesner D, Cohen FE, DeArmond SJ, Prusiner SB. Legname G, et al. Science. 2004 Jul 30;305(5684):673-6. doi: 10.1126/science.1100195. Science. 2004. PMID: 15286374

7

Molecular biology and pathogenesis of prion diseases.

Prusiner SB. Prusiner SB. Trends Biochem Sci. 1996 Dec;21(12):482-7. doi: 10.1016/s0968-0004(96)10063-3. Trends Biochem Sci. 1996. PMID: 9009832 Review.

8

Insights into Mechanisms of Transmission and Pathogenesis from Transgenic Mouse Models of Prion Diseases.

Moreno JA, Telling GC. Moreno JA, et al. Methods Mol Biol. 2017;1658:219-252. doi: 10.1007/978-1-4939-7244-9_16. Methods Mol Biol. 2017. PMID: 28861793 Free PMC article. Review.

9

Molecular biology and genetics of prion diseases.

Prusiner SB. Prusiner SB. Philos Trans R Soc Lond B Biol Sci. 1994 Mar 29;343(1306):447-63. doi: 10.1098/rstb.1994.0043. Philos Trans R Soc Lond B Biol Sci. 1994. PMID: 7913765 Review.

10

Analysis of Conformational Stability of Abnormal Prion Protein Aggregates across the Spectrum of Creutzfeldt-Jakob Disease Prions.

Cescatti M, Saverioni D, Capellari S, Tagliavini F, Kitamoto T, Ironside J, Giese A, Parchi P. Cescatti M, et al. J Virol. 2016 Jun 24;90(14):6244-6254. doi: 10.1128/JVI.00144-16. Print 2016 Jul 15. J Virol. 2016. PMID: 27122583 Free PMC article.

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