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.
220 related articles for article (PubMed ID: 37834279)
1. Elevated E200K Somatic Mutation of the Prion Protein Gene ( Won SY; Kim YC; Jeong BH Int J Mol Sci; 2023 Oct; 24(19):. PubMed ID: 37834279 [TBL] [Abstract][Full Text] [Related]
2. Creutzfeldt-Jakob disease associated with a V203I homozygous mutation in the prion protein gene. Komatsu J; Sakai K; Hamaguchi T; Sugiyama Y; Iwasa K; Yamada M Prion; 2014; 8(5):336-8. PubMed ID: 25495585 [TBL] [Abstract][Full Text] [Related]
3. Neuropathologically directed profiling of PRNP somatic and germline variants in sporadic human prion disease. McDonough GA; Cheng Y; Morillo KS; Doan RN; Zhou Z; Kenny CJ; Foutz A; Kim C; Cohen ML; Appleby BS; Walsh CA; Safar JG; Huang AY; Miller MB Acta Neuropathol; 2024 Jul; 148(1):10. PubMed ID: 39048735 [TBL] [Abstract][Full Text] [Related]
4. The First Evaluation of Proteinase K-Resistant Prion Protein (PrP Won SY; Kim YC; Lee YN; Park CG; Kim WY; Jeong BH Medicina (Kaunas); 2022 Jul; 58(7):. PubMed ID: 35888666 [No Abstract] [Full Text] [Related]
5. Human prion protein (PrP) 219K is converted to PrPSc but shows heterozygous inhibition in variant Creutzfeldt-Jakob disease infection. Hizume M; Kobayashi A; Teruya K; Ohashi H; Ironside JW; Mohri S; Kitamoto T J Biol Chem; 2009 Feb; 284(6):3603-9. PubMed ID: 19074151 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. The First Meta-Analysis of the M129V Single-Nucleotide Polymorphism (SNP) of the Prion Protein Gene ( Kim YC; Jeong BH Cells; 2021 Nov; 10(11):. PubMed ID: 34831353 [TBL] [Abstract][Full Text] [Related]
8. Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development. Mitrová E; Belay G Acta Virol; 2002; 46(1):31-9. PubMed ID: 12197632 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol. Bregman N; Shiner T; Kavé G; Alcalay R; Gana-Weisz M; Goldstein O; Glinka T; Aizenstein O; Bashat DB; Alcalay Y; Mirelman A; Thaler A; Giladi N; Omer N BMC Neurol; 2023 Apr; 23(1):151. PubMed ID: 37069531 [TBL] [Abstract][Full Text] [Related]
11. Iatrogenic and sporadic Creutzfeldt-Jakob disease in 2 sisters without mutation in the prion protein gene. Frontzek K; Moos R; Schaper E; Jann L; Herfs G; Zimmermann DR; Aguzzi A; Budka H Prion; 2015; 9(6):444-8. PubMed ID: 26634863 [TBL] [Abstract][Full Text] [Related]
13. [Creutzfeldt-Jakob encephalopathy with mutation E200K. Report of a "sporadic" case]. Cosacov RM; Taratuto AL; Ghiraridi G; Barrionuevo P; Diaz A; Begué C; Martinetto H Rev Fac Cien Med Univ Nac Cordoba; 2004; 61(1):48-53. PubMed ID: 15366237 [TBL] [Abstract][Full Text] [Related]
14. Identification of Prion Disease-Related Somatic Mutations in the Prion Protein Gene ( Kim YC; Won SY; Jeong BH Cells; 2020 Jun; 9(6):. PubMed ID: 32560489 [TBL] [Abstract][Full Text] [Related]
15. Prion protein monoclonal antibody (PRN100) therapy for Creutzfeldt-Jakob disease: evaluation of a first-in-human treatment programme. Mead S; Khalili-Shirazi A; Potter C; Mok T; Nihat A; Hyare H; Canning S; Schmidt C; Campbell T; Darwent L; Muirhead N; Ebsworth N; Hextall P; Wakeling M; Linehan J; Libri V; Williams B; Jaunmuktane Z; Brandner S; Rudge P; Collinge J Lancet Neurol; 2022 Apr; 21(4):342-354. PubMed ID: 35305340 [TBL] [Abstract][Full Text] [Related]
16. Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins. Asante EA; Gowland I; Grimshaw A; Linehan JM; Smidak M; Houghton R; Osiguwa O; Tomlinson A; Joiner S; Brandner S; Wadsworth JDF; Collinge J J Gen Virol; 2009 Mar; 90(Pt 3):546-558. PubMed ID: 19218199 [TBL] [Abstract][Full Text] [Related]
17. Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotype. Peoc'h K; Manivet P; Beaudry P; Attane F; Besson G; Hannequin D; Delasnerie-Lauprêtre N; Laplanche JL Hum Mutat; 2000 May; 15(5):482. PubMed ID: 10790216 [TBL] [Abstract][Full Text] [Related]
18. Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases. Schmitz M; Lüllmann K; Zafar S; Ebert E; Wohlhage M; Oikonomou P; Schlomm M; Mitrova E; Beekes M; Zerr I Neurobiol Aging; 2014 May; 35(5):1177-88. PubMed ID: 24360565 [TBL] [Abstract][Full Text] [Related]
19. Prion protein with an E200K mutation displays properties similar to those of the cellular isoform PrP(C). Rosenmann H; Talmor G; Halimi M; Yanai A; Gabizon R; Meiner Z J Neurochem; 2001 Mar; 76(6):1654-62. PubMed ID: 11259483 [TBL] [Abstract][Full Text] [Related]
20. Distinctive cerebellar immunoreactivity for the prion protein in familial (E200K) Creutzfeldt-Jakob disease. Jarius C; Kovacs GG; Belay G; Hainfellner JA; Mitrova E; Budka H Acta Neuropathol; 2003 May; 105(5):449-54. PubMed ID: 12677444 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]