DeArmond SJ - Search Results

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. Among authors: dearmond sj. Science. 1996 Dec 20;274(5295):2079-82. doi: 10.1126/science.274.5295.2079. Science. 1996. PMID: 8953038

2

Abbreviated incubation times for human prions in mice expressing a chimeric mouse-human prion protein transgene.

Korth C, Kaneko K, Groth D, Heye N, Telling G, Mastrianni J, Parchi P, Gambetti P, Will R, Ironside J, Heinrich C, Tremblay P, DeArmond SJ, Prusiner SB. Korth C, et al. Among authors: dearmond sj. Proc Natl Acad Sci U S A. 2003 Apr 15;100(8):4784-9. doi: 10.1073/pnas.2627989100. Epub 2003 Apr 8. Proc Natl Acad Sci U S A. 2003. PMID: 12684540 Free PMC article.

3

Perspectives on prion biology, prion disease pathogenesis, and pharmacologic approaches to treatment.

DeArmond SJ, Prusiner SB. DeArmond SJ, et al. Clin Lab Med. 2003 Mar;23(1):1-41. doi: 10.1016/s0272-2712(02)00041-0. Clin Lab Med. 2003. PMID: 12733423 Review.

4

Synthetic mammalian prions.

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

5

Regional mapping of prion proteins in brain.

Taraboulos A, Jendroska K, Serban D, Yang SL, DeArmond SJ, Prusiner SB. Taraboulos A, et al. Among authors: dearmond sj. Proc Natl Acad Sci U S A. 1992 Aug 15;89(16):7620-4. doi: 10.1073/pnas.89.16.7620. Proc Natl Acad Sci U S A. 1992. PMID: 1354357 Free PMC article.

6

Molecular biology and pathology of scrapie and the prion diseases of humans.

Prusiner SB, DeArmond SJ. Prusiner SB, et al. Among authors: dearmond sj. Brain Pathol. 1991 Jul;1(4):297-310. doi: 10.1111/j.1750-3639.1991.tb00673.x. Brain Pathol. 1991. PMID: 1669719 Review.

7

Spontaneous neurodegeneration in transgenic mice with prion protein codon 101 proline----leucine substitution.

Hsiao K, Scott M, Foster D, DeArmond SJ, Groth D, Serban H, Prusiner SB. Hsiao K, et al. Among authors: dearmond sj. Ann N Y Acad Sci. 1991;640:166-70. doi: 10.1111/j.1749-6632.1991.tb00210.x. Ann N Y Acad Sci. 1991. PMID: 1685642

8

Rapid detection of Creutzfeldt-Jakob disease and scrapie prion proteins.

Serban D, Taraboulos A, DeArmond SJ, Prusiner SB. Serban D, et al. Among authors: dearmond sj. Neurology. 1990 Jan;40(1):110-7. doi: 10.1212/wnl.40.1.110. Neurology. 1990. PMID: 1967489

9

Spontaneous neurodegeneration in transgenic mice with mutant prion protein.

Hsiao KK, Scott M, Foster D, Groth DF, DeArmond SJ, Prusiner SB. Hsiao KK, et al. Among authors: dearmond sj. Science. 1990 Dec 14;250(4987):1587-90. doi: 10.1126/science.1980379. Science. 1990. PMID: 1980379

10

Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein.

Telling GC, Scott M, Mastrianni J, Gabizon R, Torchia M, Cohen FE, DeArmond SJ, Prusiner SB. Telling GC, et al. Among authors: dearmond sj. Cell. 1995 Oct 6;83(1):79-90. doi: 10.1016/0092-8674(95)90236-8. Cell. 1995. PMID: 7553876 Free article.

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