1 Ma, J, "Wild-type PrP and a mutantassociated with prion disease are subject to retrograde transportand proteasome degradation" 98 : 14955-14960, 2001
2 Keller, J. N., "The proteasomein brain aging" 1 : 279-293, 2002
3 Dong, C. F, "The N-terminus of PrP is responsiblefor interacting with tubulin and fCJD related PrPmutants possess stronger inhibitive effect on microtubuleassembly in vitro" 480 : 83-92, 2008
4 Adams, J. M, "The Bcl-2 protein family:Arbiters of cell survival" 281 : 1322-1326, 1998
5 Carmody, R. J, "Signaling apoptosis:a radical approach" 6 : 77-, 2001
6 Cai-Min Xu, "Removal of the Glycosylation of Prion Protein Provokes Apoptosis in SF126" 한국생화학분자생물학회 40 (40): 662-669, 2007
7 Rane, N. S, "Protection from cytosolic prion protein toxicity by modulationof protein translocation" 23 : 4550-4559, 2004
8 Zanusso, G, "Proteasomaldegradation and N-terminal protease resistance of the codon145 mutant prion protein" 274 : 23396-23404, 1999
9 Prusiner, S. B, "Prions" 95 : 13363-13383, 1998
10 Ma, J, "Neurotoxicityand neurodegeneration when PrP accumulates in the cytosol" 298 : 1781-1785, 2002
1 Ma, J, "Wild-type PrP and a mutantassociated with prion disease are subject to retrograde transportand proteasome degradation" 98 : 14955-14960, 2001
2 Keller, J. N., "The proteasomein brain aging" 1 : 279-293, 2002
3 Dong, C. F, "The N-terminus of PrP is responsiblefor interacting with tubulin and fCJD related PrPmutants possess stronger inhibitive effect on microtubuleassembly in vitro" 480 : 83-92, 2008
4 Adams, J. M, "The Bcl-2 protein family:Arbiters of cell survival" 281 : 1322-1326, 1998
5 Carmody, R. J, "Signaling apoptosis:a radical approach" 6 : 77-, 2001
6 Cai-Min Xu, "Removal of the Glycosylation of Prion Protein Provokes Apoptosis in SF126" 한국생화학분자생물학회 40 (40): 662-669, 2007
7 Rane, N. S, "Protection from cytosolic prion protein toxicity by modulationof protein translocation" 23 : 4550-4559, 2004
8 Zanusso, G, "Proteasomaldegradation and N-terminal protease resistance of the codon145 mutant prion protein" 274 : 23396-23404, 1999
9 Prusiner, S. B, "Prions" 95 : 13363-13383, 1998
10 Ma, J, "Neurotoxicityand neurodegeneration when PrP accumulates in the cytosol" 298 : 1781-1785, 2002
11 Dong, C. F, "Molecular interaction between prion proteinand GFAP both in native and recombinant forms in vitro" 197 : 361-368, 2008
12 Aguzzi, A, "Mammalian prionbiology: one century of evolving concepts" 116 : 313-327, 2004
13 Perovic, S, "Effect of flupirtine on bcl-2 and glutathione level in neuronalcells treated in vitro with the prion protein fragment(PrP106-126)" 147 : 518-524, 1997
14 Kopito,R.R, "ER quality control: the cytoplasmicconnection" 88 : 427-430, 1997
15 김태형, "Differential Efflux of Mitochondrial Endonuclease G by hNoxa and tBid" 한국생화학분자생물학회 39 (39): 556-559, 2006
16 Fioriti, L, "Cytosolic prion proteinis not toxic in N2a cells and primary neurons expressingpathogenic PrP mutations" 280 : 11320-11328, 2005
17 Norstrom, E. M, "Cytosolic prion protein toxicityis independent of cellular prion protein expressionand prion propagation" 81 : 2831-2837, 2007
18 Rambold, A. S, "Association of bcl-2with misfolded prion protein is linked to the toxic potentialof cytosolic PrP" 17 : 3356-, 2006
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