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For: Foliaki ST, Lewis V, Islam AMT, Ellett LJ, Senesi M, Finkelstein DI, Roberts B, Lawson VA, Adlard PA, Collins SJ. Early existence and biochemical evolution characterise acutely synaptotoxic PrPSc. PLoS Pathog 2019;15:e1007712. [PMID: 30970042 DOI: 10.1371/journal.ppat.1007712] [Cited by in Crossref: 6] [Cited by in F6Publishing: 8] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Foliaki ST, Race B, Williams K, Baune C, Groveman BR, Haigh CL. Reduced SOD2 expression does not influence prion disease course or pathology in mice. PLoS One 2021;16:e0259597. [PMID: 34735539 DOI: 10.1371/journal.pone.0259597] [Reference Citation Analysis]
2 Cortez LM, Nemani SK, Duque Velásquez C, Sriraman A, Wang Y, Wille H, McKenzie D, Sim VL. Asymmetric-flow field-flow fractionation of prions reveals a strain-specific continuum of quaternary structures with protease resistance developing at a hydrodynamic radius of 15 nm. PLoS Pathog 2021;17:e1009703. [PMID: 34181702 DOI: 10.1371/journal.ppat.1009703] [Cited by in F6Publishing: 4] [Reference Citation Analysis]
3 Martin D, Reine F, Herzog L, Igel-Egalon A, Aron N, Michel C, Moudjou M, Fichet G, Quadrio I, Perret-Liaudet A, Andréoletti O, Rezaei H, Béringue V. Prion potentiation after life-long dormancy in mice devoid of PrP. Brain Commun 2021;3:fcab092. [PMID: 33997785 DOI: 10.1093/braincomms/fcab092] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
4 Eskandari-Sedighi G, Cortez LM, Yang J, Daude N, Shmeit K, Sim V, Westaway D. Quaternary Structure Changes for PrPSc Predate PrPC Downregulation and Neuronal Death During Progression of Experimental Scrapie Disease. Mol Neurobiol 2021;58:375-90. [PMID: 32959170 DOI: 10.1007/s12035-020-02112-z] [Cited by in F6Publishing: 4] [Reference Citation Analysis]
5 Benilova I, Reilly M, Terry C, Wenborn A, Schmidt C, Marinho AT, Risse E, Al-Doujaily H, Wiggins De Oliveira M, Sandberg MK, Wadsworth JDF, Jat PS, Collinge J. Highly infectious prions are not directly neurotoxic. Proc Natl Acad Sci U S A 2020;117:23815-22. [PMID: 32900920 DOI: 10.1073/pnas.2007406117] [Cited by in Crossref: 6] [Cited by in F6Publishing: 10] [Article Influence: 3.0] [Reference Citation Analysis]
6 Foliaki ST, Groveman BR, Yuan J, Walters R, Zhang S, Tesar P, Zou W, Haigh CL. Pathogenic Prion Protein Isoforms Are Not Present in Cerebral Organoids Generated from Asymptomatic Donors Carrying the E200K Mutation Associated with Familial Prion Disease. Pathogens 2020;9:E482. [PMID: 32570796 DOI: 10.3390/pathogens9060482] [Cited by in Crossref: 3] [Cited by in F6Publishing: 6] [Article Influence: 1.5] [Reference Citation Analysis]
7 Foliaki ST, Lewis V, Islam AMT, Senesi M, Finkelstein DI, Ellett LJ, Lawson VA, Adlard PA, Roberts BR, Collins SJ. PrPSc Oligomerization Appears Dynamic, Quickly Engendering Inherent M1000 Acute Synaptotoxicity. Biophys J 2020;119:128-41. [PMID: 32562618 DOI: 10.1016/j.bpj.2020.04.040] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
8 Igel-Egalon A, Bohl J, Moudjou M, Herzog L, Reine F, Rezaei H, Béringue V. Heterogeneity and Architecture of Pathological Prion Protein Assemblies: Time to Revisit the Molecular Basis of the Prion Replication Process? Viruses 2019;11:E429. [PMID: 31083283 DOI: 10.3390/v11050429] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 4.7] [Reference Citation Analysis]