274 related articles for article (PubMed ID: 11852147)
21. 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]
22. Prion and doppel proteins bind to granule cells of the cerebellum.
Legname G; Nelken P; Guan Z; Kanyo ZF; DeArmond SJ; Prusiner SB
Proc Natl Acad Sci U S A; 2002 Dec; 99(25):16285-90. PubMed ID: 12446843
[TBL] [Abstract][Full Text] [Related]
23. Induction of HO-1 and NOS in doppel-expressing mice devoid of PrP: implications for doppel function.
Wong BS; Liu T; Paisley D; Li R; Pan T; Chen SG; Perry G; Petersen RB; Smith MA; Melton DW; Gambetti P; Brown DR; Sy MS
Mol Cell Neurosci; 2001 Apr; 17(4):768-75. PubMed ID: 11312611
[TBL] [Abstract][Full Text] [Related]
24. The prion's elusive reason for being.
Aguzzi A; Baumann F; Bremer J
Annu Rev Neurosci; 2008; 31():439-77. PubMed ID: 18558863
[TBL] [Abstract][Full Text] [Related]
25. Molecular biology of prion protein and its first homologous protein.
Sakaguchi S
J Med Invest; 2007 Aug; 54(3-4):211-23. PubMed ID: 17878669
[TBL] [Abstract][Full Text] [Related]
26. Nonneuronal cellular prion protein.
Fournier JG
Int Rev Cytol; 2001; 208():121-60. PubMed ID: 11510567
[TBL] [Abstract][Full Text] [Related]
27. A pathogenic PrP mutation and doppel interfere with polarized sorting of the prion protein.
Uelhoff A; Tatzelt J; Aguzzi A; Winklhofer KF; Haass C
J Biol Chem; 2005 Feb; 280(7):5137-40. PubMed ID: 15615717
[TBL] [Abstract][Full Text] [Related]
28. Copper(II) binding to the human Doppel protein may mark its functional diversity from the prion protein.
Cereghetti GM; Negro A; Vinck E; Massimino ML; Sorgato MC; Van Doorslaer S
J Biol Chem; 2004 Aug; 279(35):36497-503. PubMed ID: 15218028
[TBL] [Abstract][Full Text] [Related]
29. Fusion of Doppel to octapeptide repeat and N-terminal half of hydrophobic region of prion protein confers resistance to serum deprivation.
Lee DC; Sakudo A; Kim CK; Nishimura T; Saeki K; Matsumoto Y; Yokoyama T; Chen SG; Itohara S; Onodera T
Microbiol Immunol; 2006; 50(3):203-9. PubMed ID: 16547418
[TBL] [Abstract][Full Text] [Related]
30. Prion proteins: physiological functions and role in neurological disorders.
Hu W; Kieseier B; Frohman E; Eagar TN; Rosenberg RN; Hartung HP; Stüve O
J Neurol Sci; 2008 Jan; 264(1-2):1-8. PubMed ID: 17707411
[TBL] [Abstract][Full Text] [Related]
31. Prion infection of mouse neurospheres.
Giri RK; Young R; Pitstick R; DeArmond SJ; Prusiner SB; Carlson GA
Proc Natl Acad Sci U S A; 2006 Mar; 103(10):3875-80. PubMed ID: 16495413
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Doppel: the prion's double.
Golańiska E; Flirski M; Liberski PP
Folia Neuropathol; 2004; 42 Suppl A():47-54. PubMed ID: 15449459
[TBL] [Abstract][Full Text] [Related]
34. Transgene-driven expression of the Doppel protein in Purkinje cells causes Purkinje cell degeneration and motor impairment.
Anderson L; Rossi D; Linehan J; Brandner S; Weissmann C
Proc Natl Acad Sci U S A; 2004 Mar; 101(10):3644-9. PubMed ID: 15007176
[TBL] [Abstract][Full Text] [Related]
35. Serum withdrawal-induced apoptosis in ZrchI prion protein (PrP) gene-deficient neuronal cell line is suppressed by PrP, independent of Doppel.
Nishimura T; Sakudo A; Hashiyama Y; Yachi A; Saeki K; Matsumoto Y; Ogawa M; Sakaguchi S; Itohara S; Onodera T
Microbiol Immunol; 2007; 51(4):457-66. PubMed ID: 17446686
[TBL] [Abstract][Full Text] [Related]
36. Doppel is an N-glycosylated, glycosylphosphatidylinositol-anchored protein. Expression in testis and ectopic production in the brains of Prnp(0/0) mice predisposed to Purkinje cell loss.
Silverman GL; Qin K; Moore RC; Yang Y; Mastrangelo P; Tremblay P; Prusiner SB; Cohen FE; Westaway D
J Biol Chem; 2000 Sep; 275(35):26834-41. PubMed ID: 10842180
[TBL] [Abstract][Full Text] [Related]
37. Abnormal activation of glial cells in the brains of prion protein-deficient mice ectopically expressing prion protein-like protein, PrPLP/Dpl.
Atarashi R; Sakaguchi S; Shigematsu K; Arima K; Okimura N; Yamaguchi N; Li A; Kopacek J; Katamine S
Mol Med; 2001 Dec; 7(12):803-9. PubMed ID: 11844868
[TBL] [Abstract][Full Text] [Related]
38. Altered expression of type 1 inositol 1,4,5-trisphosphate receptor in the Ngsk Prnp deficient mice.
Lee HP; Choi JK; Shin HY; Jeon YC; Jeong BH; Lee HG; Kim JI; Choi EK; Carp RI; Kim YS
Neuroscience; 2010 May; 167(3):799-808. PubMed ID: 20219645
[TBL] [Abstract][Full Text] [Related]
39. Deletion of N-terminal residues 23-88 from prion protein (PrP) abrogates the potential to rescue PrP-deficient mice from PrP-like protein/doppel-induced Neurodegeneration.
Atarashi R; Nishida N; Shigematsu K; Goto S; Kondo T; Sakaguchi S; Katamine S
J Biol Chem; 2003 Aug; 278(31):28944-9. PubMed ID: 12759361
[TBL] [Abstract][Full Text] [Related]
40. Bovine prion (PrP) and Doppel (Dpl) proteins expression after in vitro leukocyte activation or Dpl/PrP blocking.
Paltrinieri S; Spagnolo V; Giordano A; Gelmetti D; Comazzi S
J Cell Physiol; 2006 Aug; 208(2):446-50. PubMed ID: 16680758
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]