These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. Molecular typing of PrPres in human sporadic CJD brain tissue. Lewis V; Klug GM; Hill AF; Collins SJ Methods Mol Biol; 2008; 459():241-7. PubMed ID: 18576159 [TBL] [Abstract][Full Text] [Related]
3. Role of prion protein glycosylation in replication of human prions by protein misfolding cyclic amplification. Camacho MV; Telling G; Kong Q; Gambetti P; Notari S Lab Invest; 2019 Nov; 99(11):1741-1748. PubMed ID: 31249376 [TBL] [Abstract][Full Text] [Related]
4. Neuropathological and biochemical criteria to identify acquired Creutzfeldt-Jakob disease among presumed sporadic cases. Kobayashi A; Parchi P; Yamada M; Mohri S; Kitamoto T Neuropathology; 2016 Jun; 36(3):305-10. PubMed ID: 26669818 [TBL] [Abstract][Full Text] [Related]
5. Prion Strain Characterization of a Novel Subtype of Creutzfeldt-Jakob Disease. Galeno R; Di Bari MA; Nonno R; Cardone F; Sbriccoli M; Graziano S; Ingrosso L; Fiorini M; Valanzano A; Pasini G; Poleggi A; Vinci R; Ladogana A; Puopolo M; Monaco S; Agrimi U; Zanusso G; Pocchiari M J Virol; 2017 Jun; 91(11):. PubMed ID: 28298604 [TBL] [Abstract][Full Text] [Related]
6. The prion protein preference of sporadic Creutzfeldt-Jakob disease subtypes. Klemm HM; Welton JM; Masters CL; Klug GM; Boyd A; Hill AF; Collins SJ; Lawson VA J Biol Chem; 2012 Oct; 287(43):36465-72. PubMed ID: 22930754 [TBL] [Abstract][Full Text] [Related]
7. Glycoform-selective prion formation in sporadic and familial forms of prion disease. Xiao X; Yuan J; Haïk S; Cali I; Zhan Y; Moudjou M; Li B; Laplanche JL; Laude H; Langeveld J; Gambetti P; Kitamoto T; Kong Q; Brandel JP; Cobb BA; Petersen RB; Zou WQ PLoS One; 2013; 8(3):e58786. PubMed ID: 23527023 [TBL] [Abstract][Full Text] [Related]
8. Clusterin solubility and aggregation in Creutzfeldt-Jakob disease. Freixes M; Puig B; Rodríguez A; Torrejón-Escribano B; Blanco R; Ferrer I Acta Neuropathol; 2004 Oct; 108(4):295-301. PubMed ID: 15235804 [TBL] [Abstract][Full Text] [Related]
9. Insights into Mechanisms of Transmission and Pathogenesis from Transgenic Mouse Models of Prion Diseases. Moreno JA; Telling GC Methods Mol Biol; 2017; 1658():219-252. PubMed ID: 28861793 [TBL] [Abstract][Full Text] [Related]
10. Development of an Automated Capillary Immunoassay to Detect Prion Glycotypes in Creutzfeldt-Jakob Disease. Myskiw J; Lamoureux L; Peterson A; Knox D; Jansen GH; Coulthart MB; Booth SA Lab Invest; 2023 Mar; 103(3):100029. PubMed ID: 36925197 [TBL] [Abstract][Full Text] [Related]
19. Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein gene. Di Fede G; Catania M; Atzori C; Moda F; Pasquali C; Indaco A; Grisoli M; Zuffi M; Guaita MC; Testi R; Taraglio S; Sessa M; Gusmaroli G; Spinelli M; Salzano G; Legname G; Tarletti R; Godi L; Pocchiari M; Tagliavini F; Imperiale D; Giaccone G Acta Neuropathol Commun; 2019 Jan; 7(1):1. PubMed ID: 30606247 [TBL] [Abstract][Full Text] [Related]
20. Sporadic and familial CJD: classification and characterisation. Gambetti P; Kong Q; Zou W; Parchi P; Chen SG Br Med Bull; 2003; 66():213-39. PubMed ID: 14522861 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]