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.
203 related articles for article (PubMed ID: 25149502)
1. Biological network inferences for a protection mechanism against familial Creutzfeldt-Jakob disease with E200K pathogenic mutation. Lee SM; Chung M; Hwang KJ; Ju YR; Hyeon JW; Park JS; Kim CK; Choi S; Lee J; Kim SY BMC Med Genomics; 2014 Aug; 7():52. PubMed ID: 25149502 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein. Hainfellner JA; Parchi P; Kitamoto T; Jarius C; Gambetti P; Budka H Ann Neurol; 1999 Jun; 45(6):812-6. PubMed ID: 10360778 [TBL] [Abstract][Full Text] [Related]
5. Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD. Pastore M; Chin SS; Bell KL; Dong Z; Yang Q; Yang L; Yuan J; Chen SG; Gambetti P; Zou WQ Am J Pathol; 2005 Dec; 167(6):1729-38. PubMed ID: 16314483 [TBL] [Abstract][Full Text] [Related]
6. Codistribution of amyloid beta plaques and spongiform degeneration in familial Creutzfeldt-Jakob disease with the E200K-129M haplotype. Ghoshal N; Cali I; Perrin RJ; Josephson SA; Sun N; Gambetti P; Morris JC Arch Neurol; 2009 Oct; 66(10):1240-6. PubMed ID: 19822779 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. [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]
10. Prion Mutations in Republic of Republic of Korea, China, and Japan. Kim DY; Shim KH; Bagyinszky E; An SSA Int J Mol Sci; 2022 Dec; 24(1):. PubMed ID: 36614069 [TBL] [Abstract][Full Text] [Related]
11. Age at onset of genetic (E200K) and sporadic Creutzfeldt-Jakob diseases is modulated by the Poleggi A; van der Lee S; Capellari S; Puopolo M; Ladogana A; De Pascali E; Lia D; Formato A; Bartoletti-Stella A; Parchi P; van Duijn C; Pocchiari M J Neurol Neurosurg Psychiatry; 2018 Dec; 89(12):1243-1249. PubMed ID: 30032116 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. Age at Death of Creutzfeldt-Jakob disease in subsequent family generation carrying the E200K mutation of the prion protein gene. Pocchiari M; Poleggi A; Puopolo M; D'Alessandro M; Tiple D; Ladogana A PLoS One; 2013; 8(4):e60376. PubMed ID: 23565236 [TBL] [Abstract][Full Text] [Related]
14. Roles of methionine oxidation in E200K prion protein misfolding: Implications for the mechanism of pathogenesis in E200K linked familial Creutzfeldt-Jakob disease. Wang Z; Feng B; Xiao G; Zhou Z Biochim Biophys Acta; 2016 Apr; 1864(4):346-58. PubMed ID: 26779934 [TBL] [Abstract][Full Text] [Related]
15. [Genetic Creutzfeldt-Jakob disease with a glutamate-to-lysine substitution at codon 219 (E219K) in the presence of the E200K mutation presenting with rapid progressive dementia following slowly progressive clinical course]. Takayanagi M; Suzuki K; Nakamura T; Hirata K; Satoh K; Kitamoto T Rinsho Shinkeigaku; 2018 Nov; 58(11):682-687. PubMed ID: 30369528 [TBL] [Abstract][Full Text] [Related]
16. Genomic Characteristics of Genetic Creutzfeldt-Jakob Disease Patients with V180I Mutation and Associations with Other Neurodegenerative Disorders. Lee SM; Chung M; Hyeon JW; Jeong SW; Ju YR; Kim H; Lee J; Kim S; An SS; Cho SB; Lee YS; Kim SY PLoS One; 2016; 11(6):e0157540. PubMed ID: 27341347 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Japanese Creutzfeldt-Jakob disease patients exhibiting high incidence of the E200K PRNP mutation and located in the basin of a river. Miyakawa T; Inoue K; Iseki E; Kawanishi C; Sugiyama N; Onishi H; Yamada Y; Suzuki K; Iwabuchi K; Kosaka K Neurol Res; 1998 Dec; 20(8):684-8. PubMed ID: 9864731 [TBL] [Abstract][Full Text] [Related]
20. The first Chinese case of Creutzfeldt-Jakob disease with mutation of E200K in PRNP. Gao C; Shi Q; Zhou W; Tian C; Jiang HY; Han BY; Dong XP Biomed Environ Sci; 2010 Apr; 23(2):158-60. PubMed ID: 20514992 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]