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MicroRNAs in Prion Diseases-From Molecular Mechanisms to Insights in Translational Medicine.
Contiliani DF, Ribeiro YA, de Moraes VN, Pereira TC. Contiliani DF, et al. Cells. 2021 Jun 29;10(7):1620. doi: 10.3390/cells10071620. Cells. 2021. PMID: 34209482 Free PMC article. Review.
In humans, classical prion diseases include Creutzfeldt-Jakob disease, fatal familial insomnia, Gerstmann-Straussler-Scheinker syndrome, and kuru. The aim of this review is to present the connections between miRNAs and prions, exploring how the interac …
In humans, classical prion diseases include Creutzfeldt-Jakob disease, fatal familial insomnia, Gerstmann-Straussler-Schein …
Early clinical signs and imaging findings in Gerstmann-Straussler-Scheinker syndrome (Pro102Leu).
Arata H, Takashima H, Hirano R, Tomimitsu H, Machigashira K, Izumi K, Kikuno M, Ng AR, Umehara F, Arisato T, Ohkubo R, Nakabeppu Y, Nakajo M, Osame M, Arimura K. Arata H, et al. Neurology. 2006 Jun 13;66(11):1672-8. doi: 10.1212/01.wnl.0000218211.85675.18. Neurology. 2006. PMID: 16769939 Clinical Trial.
OBJECTIVE: To determine the clinical and radiologic features of Gerstmann-Straussler-Scheinker syndrome caused by Pro102Leu mutation in PRNP (GSS102). ...These studies suggested sites of pathology in GSS102, with the main lesions probably locate …
OBJECTIVE: To determine the clinical and radiologic features of Gerstmann-Straussler-Scheinker syndrome c …
Thienyl pyrimidine derivatives with PrP(Sc) oligomer-inducing activity are a promising tool to study prions.
Imberdis T, Ayrolles-Torro A, Verdier JM, Perrier V. Imberdis T, et al. Curr Top Med Chem. 2013;13(19):2477-83. doi: 10.2174/15680266113136660174. Curr Top Med Chem. 2013. PMID: 24059332 Review.
In humans, TSEs are represented by Creutzfeldt-Jakob disease (CJD), Gerstmann-Straussler-Scheinker syndrome, Fatal Familial Insomnia and Kuru. ...
In humans, TSEs are represented by Creutzfeldt-Jakob disease (CJD), Gerstmann-Straussler-Scheinker syndrome, Fat …
Upregulation of micro RNA-146a (miRNA-146a), a marker for inflammatory neurodegeneration, in sporadic Creutzfeldt-Jakob disease (sCJD) and Gerstmann-Straussler-Scheinker (GSS) syndrome.
Lukiw WJ, Dua P, Pogue AI, Eicken C, Hill JM. Lukiw WJ, et al. J Toxicol Environ Health A. 2011;74(22-24):1460-8. doi: 10.1080/15287394.2011.618973. J Toxicol Environ Health A. 2011. PMID: 22043907 Free PMC article.
This study provides evidence of upregulation of miRNA-146a in extremely rare (incidence 1-10 per 100 million) human prion-based neurodegenerative disorders, including sporadic Creutzfeldt-Jakob disease (sCJD) and Gerstmann-Straussler-Scheinker syndrome …
This study provides evidence of upregulation of miRNA-146a in extremely rare (incidence 1-10 per 100 million) human prion-based neurodegener …
Spontaneous generation of infectious prion disease in transgenic mice.
Torres JM, Castilla J, Pintado B, Gutiérrez-Adan A, Andréoletti O, Aguilar-Calvo P, Arroba AI, Parra-Arrondo B, Ferrer I, Manzanares J, Espinosa JC. Torres JM, et al. Emerg Infect Dis. 2013 Dec;19(12):1938-47. doi: 10.3201/eid1912.130106. Emerg Infect Dis. 2013. PMID: 24274622 Free PMC article.
This protein is homologous to human protein with mutation 102L, and its genetic link with Gerstmann-Straussler-Scheinker syndrome has been established. This mutation in bovine PrP(C) causes a fully penetrant, lethal, spongiform encephalopathy. ...These …
This protein is homologous to human protein with mutation 102L, and its genetic link with Gerstmann-Straussler-Scheinker …
Infective agents in fixed human cadavers: a brief review and suggested guidelines.
Demiryürek D, Bayramoğlu A, Ustaçelebi S. Demiryürek D, et al. Anat Rec. 2002 Aug 15;269(4):194-7. doi: 10.1002/ar.10143. Anat Rec. 2002. PMID: 12209557 Free article. Review.
Infectious pathogens in cadavers that present particular risks include Mycobacterium tuberculosis, hepatitis B and C, the AIDS virus HIV, and prions that cause transmissible spongiform encephalopathies such as Creutzfeldt-Jakob disease (CJD) and Gerstmann-Straussler …
Infectious pathogens in cadavers that present particular risks include Mycobacterium tuberculosis, hepatitis B and C, the AIDS virus HIV, an …
An insert mutation in the chromosome 20 amyloid precursor gene in a Gerstmann-Sträussler-Scheinker family.
Goldfarb LG, Brown P, Vrbovská A, Baron H, McCombie WR, Cathala F, Gibbs CJ Jr, Gajdusek DC. Goldfarb LG, et al. J Neurol Sci. 1992 Sep;111(2):189-94. doi: 10.1016/0022-510x(92)90067-u. J Neurol Sci. 1992. PMID: 1431985
We report the finding of an insert mutation in the chromosome 20 amyloid precursor gene in a family with neuropathologically-verified, experimentally-transmitted Gerstmann-Straussler-Scheinker syndrome (GSS). The insert consisted of 8 extra copies of a …
We report the finding of an insert mutation in the chromosome 20 amyloid precursor gene in a family with neuropathologically-verified, exper …