Cashman NR - Search Results

1

A novel Gerstmann-Sträussler-Scheinker disease mutation defines a precursor for amyloidogenic 8 kDa PrP fragments and reveals N-terminal structural changes shared by other GSS alleles.

Mercer RCC, Daude N, Dorosh L, Fu ZL, Mays CE, Gapeshina H, Wohlgemuth SL, Acevedo-Morantes CY, Yang J, Cashman NR, Coulthart MB, Pearson DM, Joseph JT, Wille H, Safar JG, Jansen GH, Stepanova M, Sykes BD, Westaway D. Mercer RCC, et al. Among authors: cashman nr. PLoS Pathog. 2018 Jan 16;14(1):e1006826. doi: 10.1371/journal.ppat.1006826. eCollection 2018 Jan. PLoS Pathog. 2018. PMID: 29338055 Free PMC article.

2

Variant Creutzfeldt-Jakob disease: a summary of current scientific knowledge in relation to public health.

Coulthart MB, Cashman NR. Coulthart MB, et al. Among authors: cashman nr. CMAJ. 2001 Jul 10;165(1):51-8. CMAJ. 2001. PMID: 11468957 Free PMC article. Review.

3

Species barriers for chronic wasting disease by in vitro conversion of prion protein.

Li L, Coulthart MB, Balachandran A, Chakrabartty A, Cashman NR. Li L, et al. Among authors: cashman nr. Biochem Biophys Res Commun. 2007 Dec 28;364(4):796-800. doi: 10.1016/j.bbrc.2007.10.087. Epub 2007 Oct 25. Biochem Biophys Res Commun. 2007. PMID: 17964288

4

Prion protein expression and release by mast cells after activation.

Haddon DJ, Hughes MR, Antignano F, Westaway D, Cashman NR, McNagny KM. Haddon DJ, et al. Among authors: cashman nr. J Infect Dis. 2009 Sep 1;200(5):827-31. doi: 10.1086/605022. J Infect Dis. 2009. PMID: 19642931

5

Prionet Canada: a network of centres of excellence for research into prions and prion diseases.

Wong M, Toth J, Haney S, Tyshenko MG, Darshan S, Krewski D, Leighton FA, Westaway D, Moore SS, Ricketts M, Cashman N. Wong M, et al. J Toxicol Environ Health A. 2009;72(17-18):1000-7. doi: 10.1080/15287390903084108. J Toxicol Environ Health A. 2009. PMID: 19697232

6

PrioNet Canada: a network of centres of excellence for research on prion diseases--ongoing and future research directions.

Wong M, Toth J, Haney S, Krewski D, Leighton FA, Ricketts M, Westaway D, Cashman N. Wong M, et al. J Toxicol Environ Health A. 2011;74(2-4):73-87. doi: 10.1080/15287394.2011.529056. J Toxicol Environ Health A. 2011. PMID: 21218336

7

Gerstmann-Straussler-Scheinker disease due to a novel prion protein gene mutation.

Hinnell C, Coulthart MB, Jansen GH, Cashman NR, Lauzon J, Clark A, Costello F, White C, Midha R, Wiebe S, Furtado S. Hinnell C, et al. Among authors: cashman nr. Neurology. 2011 Feb 1;76(5):485-7. doi: 10.1212/WNL.0b013e31820a0ab2. Neurology. 2011. PMID: 21282596 No abstract available.

8

Relative and regional stabilities of the hamster, mouse, rabbit, and bovine prion proteins toward urea unfolding assessed by nuclear magnetic resonance and circular dichroism spectroscopies.

Julien O, Chatterjee S, Bjorndahl TC, Sweeting B, Acharya S, Semenchenko V, Chakrabartty A, Pai EF, Wishart DS, Sykes BD, Cashman NR. Julien O, et al. Among authors: cashman nr. Biochemistry. 2011 Sep 6;50(35):7536-45. doi: 10.1021/bi200731e. Epub 2011 Aug 9. Biochemistry. 2011. PMID: 21800884

9

Diagnostic accuracy of cerebrospinal fluid protein markers for sporadic Creutzfeldt-Jakob disease in Canada: a 6-year prospective study.

Coulthart MB, Jansen GH, Olsen E, Godal DL, Connolly T, Choi BC, Wang Z, Cashman NR. Coulthart MB, et al. Among authors: cashman nr. BMC Neurol. 2011 Oct 27;11:133. doi: 10.1186/1471-2377-11-133. BMC Neurol. 2011. PMID: 22032272 Free PMC article.

10

The prion protein modulates A-type K+ currents mediated by Kv4.2 complexes through dipeptidyl aminopeptidase-like protein 6.

Mercer RC, Ma L, Watts JC, Strome R, Wohlgemuth S, Yang J, Cashman NR, Coulthart MB, Schmitt-Ulms G, Jhamandas JH, Westaway D. Mercer RC, et al. Among authors: cashman nr. J Biol Chem. 2013 Dec 27;288(52):37241-55. doi: 10.1074/jbc.M113.488650. Epub 2013 Nov 13. J Biol Chem. 2013. PMID: 24225951 Free PMC article.

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