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.
24. A comparative study of abnormal prion protein isoforms between Gerstmann-Sträussler-Scheinker syndrome and Creutzfeldt-Jakob disease. Furukawa H; Doh-ura K; Kikuchi H; Tateishi J; Iwaki T J Neurol Sci; 1998 Jun; 158(1):71-5. PubMed ID: 9667781 [TBL] [Abstract][Full Text] [Related]
25. A novel mechanism of phenotypic heterogeneity demonstrated by the effect of a polymorphism on a pathogenic mutation in the PRNP (prion protein gene). Petersen RB; Goldfarb LG; Tabaton M; Brown P; Monari L; Cortelli P; Montagna P; Autilio-Gambetti L; Gajdusek DC; Lugaresi E Mol Neurobiol; 1994; 8(2-3):99-103. PubMed ID: 7999319 [TBL] [Abstract][Full Text] [Related]
29. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism. Monari L; Chen SG; Brown P; Parchi P; Petersen RB; Mikol J; Gray F; Cortelli P; Montagna P; Ghetti B Proc Natl Acad Sci U S A; 1994 Mar; 91(7):2839-42. PubMed ID: 7908444 [TBL] [Abstract][Full Text] [Related]
30. Transgenic mice recapitulate the phenotypic heterogeneity of genetic prion diseases without developing prion infectivity: Role of intracellular PrP retention in neurotoxicity. Chiesa R; Restelli E; Comerio L; Del Gallo F; Imeri L Prion; 2016 Mar; 10(2):93-102. PubMed ID: 26864450 [TBL] [Abstract][Full Text] [Related]
31. Corticobasal manifestations of Creutzfeldt-Jakob disease with D178N-homozygous 129M genotype. Huang Y; Jianfang M; Morales R; Tang H Prion; 2020 Dec; 14(1):232-237. PubMed ID: 32946318 [TBL] [Abstract][Full Text] [Related]
32. [A trend of molecular genetics on prion diseases and prion protein]. Muramatsu Y; Shinagawa M Nihon Rinsho; 1993 Sep; 51(9):2494-502. PubMed ID: 8411733 [TBL] [Abstract][Full Text] [Related]
33. Profoundly different prion diseases in knock-in mice carrying single PrP codon substitutions associated with human diseases. Jackson WS; Borkowski AW; Watson NE; King OD; Faas H; Jasanoff A; Lindquist S Proc Natl Acad Sci U S A; 2013 Sep; 110(36):14759-64. PubMed ID: 23959875 [TBL] [Abstract][Full Text] [Related]
34. D178N, 129Val and N171S, 129Val genotype in a family with Creutzfeldt-Jakob disease. Appleby BS; Appleby KK; Hall RC; Wallin MT Dement Geriatr Cogn Disord; 2010; 30(5):424-31. PubMed ID: 21071944 [TBL] [Abstract][Full Text] [Related]
35. Molecular genetics of human prion diseases in Germany. Windl O; Giese A; Schulz-Schaeffer W; Zerr I; Skworc K; Arendt S; Oberdieck C; Bodemer M; Poser S; Kretzschmar HA Hum Genet; 1999 Sep; 105(3):244-52. PubMed ID: 10987652 [TBL] [Abstract][Full Text] [Related]