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Items: 1 to 20 of 83

1.

C-terminal peptides modelling constitutive PrPC processing demonstrate ameliorated toxicity predisposition consequent to α-cleavage.

Johanssen VA, Johanssen T, Masters CL, Hill AF, Barnham KJ, Collins SJ.

Biochem J. 2014 Apr 1;459(1):103-15. doi: 10.1042/BJ20131378.

PMID:
24438129
2.

PrP(C) homodimerization stimulates the production of PrPC cleaved fragments PrPN1 and PrPC1.

Béland M, Motard J, Barbarin A, Roucou X.

J Neurosci. 2012 Sep 19;32(38):13255-63.

3.

Generating recombinant C-terminal prion protein fragments of exact native sequence.

Johanssen VA, Barnham KJ, Masters CL, Hill AF, Collins SJ.

Neurochem Int. 2012 Feb;60(3):318-26. doi: 10.1016/j.neuint.2011.12.006. Epub 2011 Dec 17.

PMID:
22197912
4.

PrPC-related signal transduction is influenced by copper, membrane integrity and the alpha cleavage site.

Haigh CL, Lewis VA, Vella LJ, Masters CL, Hill AF, Lawson VA, Collins SJ.

Cell Res. 2009 Sep;19(9):1062-78. doi: 10.1038/cr.2009.86. Epub 2009 Jul 14.

PMID:
19597535
5.
6.

Endoproteolytic processing of the mammalian prion glycoprotein family.

Mays CE, Coomaraswamy J, Watts JC, Yang J, Ko KW, Strome B, Mercer RC, Wohlgemuth SL, Schmitt-Ulms G, Westaway D.

FEBS J. 2014 Feb;281(3):862-76. doi: 10.1111/febs.12654. Epub 2013 Dec 23.

7.

The interaction of humic substances with the human prion protein fragment 90-231 affects its protease K resistance and cell internalization.

Corsaro A, Anselmi C, Polano M, Aceto A, Florio T, De Nobili M.

J Biol Regul Homeost Agents. 2010 Jan-Mar;24(1):27-39.

PMID:
20385069
8.

Prion protein "gamma-cleavage": characterizing a novel endoproteolytic processing event.

Lewis V, Johanssen VA, Crouch PJ, Klug GM, Hooper NM, Collins SJ.

Cell Mol Life Sci. 2016 Feb;73(3):667-83. doi: 10.1007/s00018-015-2022-z. Epub 2015 Aug 23.

PMID:
26298290
9.

The cellular prion protein mediates neurotoxic signalling of β-sheet-rich conformers independent of prion replication.

Resenberger UK, Harmeier A, Woerner AC, Goodman JL, Müller V, Krishnan R, Vabulas RM, Kretzschmar HA, Lindquist S, Hartl FU, Multhaup G, Winklhofer KF, Tatzelt J.

EMBO J. 2011 May 18;30(10):2057-70. doi: 10.1038/emboj.2011.86. Epub 2011 Mar 25.

10.

Prion peptide 106-126 as a model for prion replication and neurotoxicity.

Singh N, Gu Y, Bose S, Kalepu S, Mishra RS, Verghese S.

Front Biosci. 2002 Apr 1;7:a60-71.

PMID:
11897566
11.

Recombinant human prion protein mutants huPrP D178N/M129 (FFI) and huPrP+9OR (fCJD) reveal proteinase K resistance.

Gauczynski S, Krasemann S, Bodemer W, Weiss S.

J Cell Sci. 2002 Nov 1;115(Pt 21):4025-36.

12.

Alpha- and beta- cleavages of the amino-terminus of the cellular prion protein.

Mangé A, Béranger F, Peoc'h K, Onodera T, Frobert Y, Lehmann S.

Biol Cell. 2004 Mar;96(2):125-32.

PMID:
15050367
13.

Mouse cortical cells lacking cellular PrP survive in culture with a neurotoxic PrP fragment.

Brown DR, Herms J, Kretzschmar HA.

Neuroreport. 1994 Oct 27;5(16):2057-60.

PMID:
7865744
14.

A new paradigm for enzymatic control of α-cleavage and β-cleavage of the prion protein.

McDonald AJ, Dibble JP, Evans EG, Millhauser GL.

J Biol Chem. 2014 Jan 10;289(2):803-13. doi: 10.1074/jbc.M113.502351. Epub 2013 Nov 18.

15.

Calpain-dependent endoproteolytic cleavage of PrPSc modulates scrapie prion propagation.

Yadavalli R, Guttmann RP, Seward T, Centers AP, Williamson RA, Telling GC.

J Biol Chem. 2004 May 21;279(21):21948-56. Epub 2004 Mar 16.

16.

Lymphocyte toxicity of prion fragments.

Murali J, Jayakumar R.

J Biochem. 2006 Mar;139(3):329-38.

PMID:
16567397
17.

Role of microglia and host prion protein in neurotoxicity of a prion protein fragment.

Brown DR, Schmidt B, Kretzschmar HA.

Nature. 1996 Mar 28;380(6572):345-7.

PMID:
8598929
18.
19.

Altered expression of the prion gene in rat astrocyte and neuron cultures treated with prion peptide 106-126.

Ning ZY, Zhao DM, Liu HX, Yang JM, Han CX, Cui YL, Meng LP, Wu CD, Liu ML, Zhang TX.

Cell Mol Neurobiol. 2005 Dec;25(8):1171-83.

PMID:
16388330
20.

Prion protein-deficient cells show altered response to oxidative stress due to decreased SOD-1 activity.

Brown DR, Schulz-Schaeffer WJ, Schmidt B, Kretzschmar HA.

Exp Neurol. 1997 Jul;146(1):104-12.

PMID:
9225743

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