315 related articles for article (PubMed ID: 28851903)
21. Prion protein (PrP) knock-out mice show altered iron metabolism: a functional role for PrP in iron uptake and transport.
Singh A; Kong Q; Luo X; Petersen RB; Meyerson H; Singh N
PLoS One; 2009 Jul; 4(7):e6115. PubMed ID: 19568430
[TBL] [Abstract][Full Text] [Related]
22. The retention of prion protein in the endoplasmic reticulum prevents N2A cells from proteasome inhibition-induced cytotoxicity.
Fang S; Wang R; Liu H; Zhuang W; Wang Z; Zhang J; Pei L; Liu Y; Su Y
Biochem Biophys Res Commun; 2017 Sep; 491(2):500-507. PubMed ID: 28669732
[TBL] [Abstract][Full Text] [Related]
23. The role of GPI-anchored PrP C in mediating the neurotoxic effect of scrapie prions in neurons.
Radford HE; Mallucci GR
Curr Issues Mol Biol; 2010; 12(2):119-27. PubMed ID: 19767655
[TBL] [Abstract][Full Text] [Related]
24. The protease-sensitive N-terminal polybasic region of prion protein modulates its conversion to the pathogenic prion conformer.
Zhang X; Pan YH; Chen Y; Pan C; Ma J; Yuan C; Yu G; Ma J
J Biol Chem; 2021 Nov; 297(5):101344. PubMed ID: 34710372
[TBL] [Abstract][Full Text] [Related]
25. Alpha-synuclein modulates retinal iron homeostasis by facilitating the uptake of transferrin-bound iron: Implications for visual manifestations of Parkinson's disease.
Baksi S; Tripathi AK; Singh N
Free Radic Biol Med; 2016 Aug; 97():292-306. PubMed ID: 27343690
[TBL] [Abstract][Full Text] [Related]
26. [Mechanisms of prion transmission].
Sakaguchi S
Nihon Rinsho; 2007 Aug; 65(8):1391-5. PubMed ID: 17695274
[TBL] [Abstract][Full Text] [Related]
27. Copper binding to PrPC may inhibit prion disease propagation.
Hijazi N; Shaked Y; Rosenmann H; Ben-Hur T; Gabizon R
Brain Res; 2003 Dec; 993(1-2):192-200. PubMed ID: 14642846
[TBL] [Abstract][Full Text] [Related]
28. Prion protein conversion induced by trivalent iron in vesicular trafficking.
Choi BR; Lee J; Kim SY; Yim I; Kim EH; Woo HJ
Biochem Biophys Res Commun; 2013 Mar; 432(3):539-44. PubMed ID: 23416082
[TBL] [Abstract][Full Text] [Related]
29. Trapping prion protein in the endoplasmic reticulum impairs PrPC maturation and prevents PrPSc accumulation.
Cardinale A; Filesi I; Vetrugno V; Pocchiari M; Sy MS; Biocca S
J Biol Chem; 2005 Jan; 280(1):685-94. PubMed ID: 15513919
[TBL] [Abstract][Full Text] [Related]
30. Temporal Resolution of Misfolded Prion Protein Transport, Accumulation, Glial Activation, and Neuronal Death in the Retinas of Mice Inoculated with Scrapie.
West Greenlee MH; Lind M; Kokemuller R; Mammadova N; Kondru N; Manne S; Smith J; Kanthasamy A; Greenlee J
Am J Pathol; 2016 Sep; 186(9):2302-9. PubMed ID: 27521336
[TBL] [Abstract][Full Text] [Related]
31. Critical significance of the region between Helix 1 and 2 for efficient dominant-negative inhibition by conversion-incompetent prion protein.
Taguchi Y; Mistica AM; Kitamoto T; Schätzl HM
PLoS Pathog; 2013; 9(6):e1003466. PubMed ID: 23825952
[TBL] [Abstract][Full Text] [Related]
32. Prion protein regulates iron transport by functioning as a ferrireductase.
Singh A; Haldar S; Horback K; Tom C; Zhou L; Meyerson H; Singh N
J Alzheimers Dis; 2013; 35(3):541-52. PubMed ID: 23478311
[TBL] [Abstract][Full Text] [Related]
33. Crossing Species Barriers Relies on Structurally Distinct Prion Assemblies and Their Complementation.
Igel-Egalon A; Laferrière F; Tixador P; Moudjou M; Herzog L; Reine F; Torres JM; Laude H; Rezaei H; Béringue V
Mol Neurobiol; 2020 Jun; 57(6):2572-2587. PubMed ID: 32239450
[TBL] [Abstract][Full Text] [Related]
34. Prion protein and metal interaction: physiological and pathological implications.
Singh N; Das D; Singh A; Mohan ML
Curr Issues Mol Biol; 2010; 12(2):99-107. PubMed ID: 19767653
[TBL] [Abstract][Full Text] [Related]
35. Discriminating between cellular and misfolded prion protein by using affinity to 9-aminoacridine compounds.
Phuan PW; Zorn JA; Safar J; Giles K; Prusiner SB; Cohen FE; May BCH
J Gen Virol; 2007 Apr; 88(Pt 4):1392-1401. PubMed ID: 17374787
[TBL] [Abstract][Full Text] [Related]
36. Sheep scrapie susceptibility-linked polymorphisms do not modulate the initial binding of cellular to disease-associated prion protein prior to conversion.
Rigter A; Bossers A
J Gen Virol; 2005 Sep; 86(Pt 9):2627-2634. PubMed ID: 16099922
[TBL] [Abstract][Full Text] [Related]
37. Manganese upregulates cellular prion protein and contributes to altered stabilization and proteolysis: relevance to role of metals in pathogenesis of prion disease.
Choi CJ; Anantharam V; Martin DP; Nicholson EM; Richt JA; Kanthasamy A; Kanthasamy AG
Toxicol Sci; 2010 Jun; 115(2):535-46. PubMed ID: 20176619
[TBL] [Abstract][Full Text] [Related]
38. Monoacylated cellular prion protein modifies cell membranes, inhibits cell signaling, and reduces prion formation.
Bate C; Williams A
J Biol Chem; 2011 Mar; 286(11):8752-8. PubMed ID: 21212283
[TBL] [Abstract][Full Text] [Related]
39. Utility of RNAi-mediated prnp gene silencing in neuroblastoma cells permanently infected by prions: potentials and limitations.
Kim Y; Han B; Titlow W; Mays CE; Kwon M; Ryou C
Antiviral Res; 2009 Nov; 84(2):185-93. PubMed ID: 19748523
[TBL] [Abstract][Full Text] [Related]
40. Tissue plasminogen activator in brain tissues infected with transmissible spongiform encephalopathies.
Xanthopoulos K; Paspaltsis I; Apostolidou V; Petrakis S; Siao CJ; Kalpatsanidis A; Grigoriadis N; Tsaftaris A; Tsirka SE; Sklaviadis T
Neurobiol Dis; 2005 Nov; 20(2):519-27. PubMed ID: 15922607
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]