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For: Davenport KA, Henderson DM, Mathiason CK, Hoover EA. Assessment of the PrPc Amino-Terminal Domain in Prion Species Barriers. J Virol 2016;90:10752-61. [PMID: 27654299 DOI: 10.1128/JVI.01121-16] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 1.3] [Reference Citation Analysis]
Number Citing Articles
1 Legname G. Prions. Reference Module in Life Sciences 2022. [DOI: 10.1016/b978-0-12-821618-7.00232-7] [Reference Citation Analysis]
2 McNulty EE, Nalls AV, Xun R, Denkers ND, Hoover EA, Mathiason CK. In vitro detection of haematogenous prions in white-tailed deer orally dosed with low concentrations of chronic wasting disease. J Gen Virol 2020;101:347-61. [PMID: 31846418 DOI: 10.1099/jgv.0.001367] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
3 Burke CM, Mark KMK, Walsh DJ, Noble GP, Steele AD, Diack AB, Manson JC, Watts JC, Supattapone S. Identification of a homology-independent linchpin domain controlling mouse and bank vole prion protein conversion. PLoS Pathog 2020;16:e1008875. [PMID: 32898162 DOI: 10.1371/journal.ppat.1008875] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
4 Hannaoui S, Arifin MI, Chang SC, Yu J, Gopalakrishnan P, Doh-Ura K, Schatzl HM, Gilch S. Cellulose ether treatment in vivo generates chronic wasting disease prions with reduced protease resistance and delayed disease progression. J Neurochem 2020;152:727-40. [PMID: 31553058 DOI: 10.1111/jnc.14877] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 2.7] [Reference Citation Analysis]
5 Bernardi L, Bruni AC. Mutations in Prion Protein Gene: Pathogenic Mechanisms in C-Terminal vs. N-Terminal Domain, a Review. Int J Mol Sci 2019;20:E3606. [PMID: 31340582 DOI: 10.3390/ijms20143606] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 3.7] [Reference Citation Analysis]
6 Davenport KA, Hoover CE, Denkers ND, Mathiason CK, Hoover EA. Modified Protein Misfolding Cyclic Amplification Overcomes Real-Time Quaking-Induced Conversion Assay Inhibitors in Deer Saliva To Detect Chronic Wasting Disease Prions. J Clin Microbiol 2018;56:e00947-18. [PMID: 29950332 DOI: 10.1128/JCM.00947-18] [Cited by in Crossref: 14] [Cited by in F6Publishing: 18] [Article Influence: 3.5] [Reference Citation Analysis]
7 Hoover CE, Davenport KA, Henderson DM, Zabel MD, Hoover EA. Endogenous Brain Lipids Inhibit Prion Amyloid Formation In Vitro. J Virol 2017;91:e02162-16. [PMID: 28202758 DOI: 10.1128/JVI.02162-16] [Cited by in Crossref: 16] [Cited by in F6Publishing: 18] [Article Influence: 3.2] [Reference Citation Analysis]
8 Hwang S, Greenlee JJ, Nicholson EM. Use of bovine recombinant prion protein and real-time quaking-induced conversion to detect cattle transmissible mink encephalopathy prions and discriminate classical and atypical L- and H-Type bovine spongiform encephalopathy. PLoS One 2017;12:e0172391. [PMID: 28225797 DOI: 10.1371/journal.pone.0172391] [Cited by in Crossref: 19] [Cited by in F6Publishing: 19] [Article Influence: 3.8] [Reference Citation Analysis]