229 related articles for article (PubMed ID: 19283067)
21. Prion Protein-Hemin Interaction Upregulates Hemoglobin Synthesis: Implications for Cerebral Hemorrhage and Sporadic Creutzfeldt-Jakob Disease.
Tripathi AK; Singh N
J Alzheimers Dis; 2016; 51(1):107-21. PubMed ID: 26836195
[TBL] [Abstract][Full Text] [Related]
22. Decrease of RyR2 in the prion infected cell line and in the brains of the scrapie infected mice models and the patients of human prion diseases.
Shi Q; Li JL; Ma Y; Gao LP; Xiao K; Wang J; Zhou W; Chen C; Guo YJ; Dong XP
Prion; 2018; 12(3-4):175-184. PubMed ID: 29676187
[TBL] [Abstract][Full Text] [Related]
23. Analyses of protease resistance and aggregation state of abnormal prion protein across the spectrum of human prions.
Saverioni D; Notari S; Capellari S; Poggiolini I; Giese A; Kretzschmar HA; Parchi P
J Biol Chem; 2013 Sep; 288(39):27972-85. PubMed ID: 23897825
[TBL] [Abstract][Full Text] [Related]
24. Development of oligomeric prion-protein aggregates in a mouse model of prion disease.
Sasaki K; Minaki H; Iwaki T
J Pathol; 2009 Sep; 219(1):123-30. PubMed ID: 19479969
[TBL] [Abstract][Full Text] [Related]
25. Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics.
Cali I; Castellani R; Alshekhlee A; Cohen Y; Blevins J; Yuan J; Langeveld JP; Parchi P; Safar JG; Zou WQ; Gambetti P
Brain; 2009 Oct; 132(Pt 10):2643-58. PubMed ID: 19734292
[TBL] [Abstract][Full Text] [Related]
26. Minimal change prion retinopathy: Morphometric comparison of retinal and brain prion deposits in Creutzfeldt-Jakob disease.
Goodwill VS; Dryden I; Choi J; De Lillo C; Soldau K; Llibre-Guerra J; Sanchez H; Sigurdson CJ; Lin JH
Exp Eye Res; 2022 Sep; 222():109172. PubMed ID: 35803332
[TBL] [Abstract][Full Text] [Related]
27. Altered Ca
Llorens F; Thüne K; Sikorska B; Schmitz M; Tahir W; Fernández-Borges N; Cramm M; Gotzmann N; Carmona M; Streichenberger N; Michel U; Zafar S; Schuetz AL; Rajput A; Andréoletti O; Bonn S; Fischer A; Liberski PP; Torres JM; Ferrer I; Zerr I
Acta Neuropathol Commun; 2017 Apr; 5(1):35. PubMed ID: 28449707
[TBL] [Abstract][Full Text] [Related]
28. Upregulation of brain hepcidin in prion diseases.
Chaudhary S; Ashok A; Wise AS; Rana NA; McDonald D; Kritikos AE; Kong Q; Singh N
Prion; 2021 Dec; 15(1):126-137. PubMed ID: 34224321
[TBL] [Abstract][Full Text] [Related]
29. The prion-ZIP connection: From cousins to partners in iron uptake.
Singh N; Asthana A; Baksi S; Desai V; Haldar S; Hari S; Tripathi AK
Prion; 2015; 9(6):420-8. PubMed ID: 26689487
[TBL] [Abstract][Full Text] [Related]
30. Neurometals in the Pathogenesis of Prion Diseases.
Kawahara M; Kato-Negishi M; Tanaka KI
Int J Mol Sci; 2021 Jan; 22(3):. PubMed ID: 33525334
[TBL] [Abstract][Full Text] [Related]
31. Early appearance but lagged accumulation of detergent-insoluble prion protein in the brains of mice inoculated with a mouse-adapted Creutzfeldt-Jakob disease agent.
Nakaoke R; Sakaguchi S; Atarashi R; Nishida N; Arima K; Shigematsu K; Katamine S
Cell Mol Neurobiol; 2000 Dec; 20(6):717-30. PubMed ID: 11100979
[TBL] [Abstract][Full Text] [Related]
32. Sc237 hamster PrPSc and Sc237-derived mouse PrPSc generated by interspecies in vitro amplification exhibit distinct pathological and biochemical properties in tga20 transgenic mice.
Yoshioka M; Imamura M; Okada H; Shimozaki N; Murayama Y; Yokoyama T; Mohri S
Microbiol Immunol; 2011 May; 55(5):331-40. PubMed ID: 21362027
[TBL] [Abstract][Full Text] [Related]
33. Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes.
Faucheux BA; Morain E; Diouron V; Brandel JP; Salomon D; Sazdovitch V; Privat N; Laplanche JL; Hauw JJ; Haïk S
Neuropathol Appl Neurobiol; 2011 Aug; 37(5):500-12. PubMed ID: 21450052
[TBL] [Abstract][Full Text] [Related]
34. Changed iron regulation in scrapie-infected neuroblastoma cells.
Fernaeus S; Hälldin J; Bedecs K; Land T
Brain Res Mol Brain Res; 2005 Feb; 133(2):266-73. PubMed ID: 15710243
[TBL] [Abstract][Full Text] [Related]
35. A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report.
Rodríguez-Martínez AB; Garrido JM; Zarranz JJ; Arteagoitia JM; de Pancorbo MM; Atarés B; Bilbao MJ; Ferrer I; Juste RA
BMC Neurol; 2010 Oct; 10():99. PubMed ID: 20973975
[TBL] [Abstract][Full Text] [Related]
36. RhoA/ROCK Regulates Prion Pathogenesis by Controlling Connexin 43 Activity.
Kim HJ; Kim MJ; Mostafa MN; Park JH; Choi HS; Kim YS; Choi EK
Int J Mol Sci; 2020 Feb; 21(4):. PubMed ID: 32070020
[TBL] [Abstract][Full Text] [Related]
37. Uptake and degradation of protease-sensitive and -resistant forms of abnormal human prion protein aggregates by human astrocytes.
Choi YP; Head MW; Ironside JW; Priola SA
Am J Pathol; 2014 Dec; 184(12):3299-307. PubMed ID: 25280631
[TBL] [Abstract][Full Text] [Related]
38. Two-dimensional mapping of three phenotype-associated isoforms of the prion protein in sporadic Creutzfeldt-Jakob disease.
Zanusso G; Righetti PG; Ferrari S; Terrin L; Farinazzo A; Cardone F; Pocchiari M; Rizzuto N; Monaco S
Electrophoresis; 2002 Jan; 23(2):347-55. PubMed ID: 11840543
[TBL] [Abstract][Full Text] [Related]
39. Aggresome formation by mutant prion proteins: the unfolding role of proteasomes in familial prion disorders.
Mishra RS; Bose S; Gu Y; Li R; Singh N
J Alzheimers Dis; 2003 Feb; 5(1):15-23. PubMed ID: 12590162
[TBL] [Abstract][Full Text] [Related]
40. Identification of distinct N-terminal truncated forms of prion protein in different Creutzfeldt-Jakob disease subtypes.
Zanusso G; Farinazzo A; Prelli F; Fiorini M; Gelati M; Ferrari S; Righetti PG; Rizzuto N; Frangione B; Monaco S
J Biol Chem; 2004 Sep; 279(37):38936-42. PubMed ID: 15247220
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
