159 related articles for article (PubMed ID: 12759361)
41. Small is not beautiful: antagonizing functions for the prion protein PrP(C) and its homologue Dpl.
Behrens A; Aguzzi A
Trends Neurosci; 2002 Mar; 25(3):150-4. PubMed ID: 11852147
[TBL] [Abstract][Full Text] [Related]
42. Truncated prion protein and Doppel are myelinotoxic in the absence of oligodendrocytic PrPC.
Radovanovic I; Braun N; Giger OT; Mertz K; Miele G; Prinz M; Navarro B; Aguzzi A
J Neurosci; 2005 May; 25(19):4879-88. PubMed ID: 15888663
[TBL] [Abstract][Full Text] [Related]
43. Propagation of prions with artificial properties in transgenic mice expressing chimeric PrP genes.
Scott M; Groth D; Foster D; Torchia M; Yang SL; DeArmond SJ; Prusiner SB
Cell; 1993 Jun; 73(5):979-88. PubMed ID: 8098995
[TBL] [Abstract][Full Text] [Related]
44. Differential responses of neuronal and spermatogenic cells to the doppel cytotoxicity.
Qin K; Ding T; Xiao Y; Ma W; Wang Z; Gao J; Zhao L
PLoS One; 2013; 8(12):e82130. PubMed ID: 24339999
[TBL] [Abstract][Full Text] [Related]
45. Physiological and pathological functions of the prion protein homologue Dpl.
Behrens A
Br Med Bull; 2003; 66():35-42. PubMed ID: 14522847
[TBL] [Abstract][Full Text] [Related]
46. Prion protein on astrocytes or in extracellular fluid impedes neurodegeneration induced by truncated prion protein.
Race B; Meade-White K; Race R; Baumann F; Aguzzi A; Chesebro B
Exp Neurol; 2009 Jun; 217(2):347-52. PubMed ID: 19332059
[TBL] [Abstract][Full Text] [Related]
47. Prion protein of 106 residues creates an artifical transmission barrier for prion replication in transgenic mice.
Supattapone S; Bosque P; Muramoto T; Wille H; Aagaard C; Peretz D; Nguyen HO; Heinrich C; Torchia M; Safar J; Cohen FE; DeArmond SJ; Prusiner SB; Scott M
Cell; 1999 Mar; 96(6):869-78. PubMed ID: 10102274
[TBL] [Abstract][Full Text] [Related]
48. NMR solution structure and SRP54M predicted interaction of the N-terminal sequence (1-30) of the ovine Doppel protein.
Pimenta J; Viegas A; Sardinha J; Martins IC; Cabrita EJ; Fontes CM; Prates JA; Pereira RM
Peptides; 2013 Nov; 49():32-40. PubMed ID: 23973967
[TBL] [Abstract][Full Text] [Related]
49. Expression of amino-terminally truncated PrP in the mouse leading to ataxia and specific cerebellar lesions.
Shmerling D; Hegyi I; Fischer M; Blättler T; Brandner S; Götz J; Rülicke T; Flechsig E; Cozzio A; von Mering C; Hangartner C; Aguzzi A; Weissmann C
Cell; 1998 Apr; 93(2):203-14. PubMed ID: 9568713
[TBL] [Abstract][Full Text] [Related]
50. PrP N-terminal domain triggers PrP(Sc)-like aggregation of Dpl.
Erlich P; Cesbron JY; Lemaire-Vieille C; Curt A; Andrieu JP; Schoehn G; Jamin M; Gagnon J
Biochem Biophys Res Commun; 2008 Jan; 365(3):478-83. PubMed ID: 17997980
[TBL] [Abstract][Full Text] [Related]
51. Newly established in vitro system with fluorescent proteins shows that abnormal expression of downstream prion protein-like protein in mice is probably due to functional disconnection between splicing and 3' formation of prion protein pre-mRNA.
Yoshikawa D; Kopacek J; Yamaguchi N; Ishibashi D; Yamanaka H; Yamaguchi Y; Katamine S; Sakaguchi S
Gene; 2007 Jan; 386(1-2):139-46. PubMed ID: 17034959
[TBL] [Abstract][Full Text] [Related]
52. Doppel-induced cytotoxicity in human neuronal SH-SY5Y cells is antagonized by the prion protein.
Li P; Dong C; Lei Y; Shan B; Xiao X; Jiang H; Wang X; Gao C; Shi Q; Xu K; Tian C; Han J; Dong X
Acta Biochim Biophys Sin (Shanghai); 2009 Jan; 41(1):42-53. PubMed ID: 19129949
[TBL] [Abstract][Full Text] [Related]
53. Impairment of superoxide dismutase activation by N-terminally truncated prion protein (PrP) in PrP-deficient neuronal cell line.
Sakudo A; Lee DC; Saeki K; Nakamura Y; Inoue K; Matsumoto Y; Itohara S; Onodera T
Biochem Biophys Res Commun; 2003 Aug; 308(3):660-7. PubMed ID: 12914801
[TBL] [Abstract][Full Text] [Related]
54. Prion protein protects mice from lethal infection with influenza A viruses.
Chida J; Hara H; Yano M; Uchiyama K; Das NR; Takahashi E; Miyata H; Tomioka Y; Ito T; Kido H; Sakaguchi S
PLoS Pathog; 2018 May; 14(5):e1007049. PubMed ID: 29723291
[TBL] [Abstract][Full Text] [Related]
55. Expression of the Prion Protein Family Member Shadoo Causes Drug Hypersensitivity That Is Diminished by the Coexpression of the Wild Type Prion Protein.
Nyeste A; Bencsura P; Vida I; Hegyi Z; Homolya L; Fodor E; Welker E
J Biol Chem; 2016 Feb; 291(9):4473-86. PubMed ID: 26721882
[TBL] [Abstract][Full Text] [Related]
56. The neurotoxicity of prion protein (PrP) peptide 106-126 is independent of the expression level of PrP and is not mediated by abnormal PrP species.
Fioriti L; Quaglio E; Massignan T; Colombo L; Stewart RS; Salmona M; Harris DA; Forloni G; Chiesa R
Mol Cell Neurosci; 2005 Jan; 28(1):165-76. PubMed ID: 15607951
[TBL] [Abstract][Full Text] [Related]
57. A mouse prion protein transgene rescues mice deficient for the prion protein gene from purkinje cell degeneration and demyelination.
Nishida N; Tremblay P; Sugimoto T; Shigematsu K; Shirabe S; Petromilli C; Erpel SP; Nakaoke R; Atarashi R; Houtani T; Torchia M; Sakaguchi S; DeArmond SJ; Prusiner SB; Katamine S
Lab Invest; 1999 Jun; 79(6):689-97. PubMed ID: 10378511
[TBL] [Abstract][Full Text] [Related]
58. Disruption of Doppel prevents neurodegeneration in mice with extensive Prnp deletions.
Genoud N; Behrens A; Miele G; Robay D; Heppner FL; Freigang S; Aguzzi A
Proc Natl Acad Sci U S A; 2004 Mar; 101(12):4198-203. PubMed ID: 15007175
[TBL] [Abstract][Full Text] [Related]
59. Normal neurogenesis and scrapie pathogenesis in neural grafts lacking the prion protein homologue Doppel.
Behrens A; Brandner S; Genoud N; Aguzzi A
EMBO Rep; 2001 Apr; 2(4):347-52. PubMed ID: 11306558
[TBL] [Abstract][Full Text] [Related]
60. Analysis of doppel protein toxicity.
Cui T; Holme A; Sassoon J; Brown DR
Mol Cell Neurosci; 2003 May; 23(1):144-55. PubMed ID: 12799144
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
