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The Journal of Infectious Diseases|November 23, 2013
Cycline efficacy on the propagation of human prions in primary cultured neurons is strain-specificSamia Hannaoui, Alexianne Gougerot, Nicolas Privat, et al.Acta Neuropathologica|August 22, 2022
Transmission of cervid prions to humanized mice demonstrates the zoonotic potential of CWDSamia Hannaoui, Irina Zemlyankina, Sheng Chun Chang, et al.Plos Pathogens|July 8, 2024
Extraneural infection route restricts prion conformational variability and attenuates the impact of quaternary structure on infectivitySheng Chun Chang, Maria Immaculata Arifin, Waqas Tahir, et al.The Journal of Biological Chemistry|August 20, 2017
Region-specific protein misfolding cyclic amplification reproduces brain tropism of prion strainsNicolas Privat, Etienne Levavasseur, Serfildan Yildirim, et al.Journal of Neurochemistry|September 26, 2019
Cellulose ether treatment in vivo generates chronic wasting disease prions with reduced protease resistance and delayed disease progressionSamia Hannaoui, Maria Immaculata Arifin, Sheng Chun Chang, et al.Acta Neuropathologica Communications|April 2, 2021
Oral administration of repurposed drug targeting Cyp46A1 increases survival times of prion infected miceTahir Ali, Samia Hannaoui, Satish Nemani, et al.Proceedings of the National Academy of Sciences of the United States of America|April 4, 2023
Heterozygosity for cervid S138N polymorphism results in subclinical CWD in gene-targeted mice and progressive inhibition of prion conversionMaria I Arifin, Lech Kaczmarczyk, Doris Zeng, et al.Plos Pathogens|August 12, 2017
Destabilizing polymorphism in cervid prion protein hydrophobic core determines prion conformation and conversion efficiencySamia Hannaoui, Sara Amidian, Yo Ching Cheng, et al.Plos Pathogens|July 26, 2021
New and distinct chronic wasting disease strains associated with cervid polymorphism at codon 116 of the Prnp geneSamia Hannaoui, Elizabeth Triscott, Camilo Duque Velásquez, et al.Plos Pathogens|July 1, 2024
Norwegian moose CWD induces clinical disease and neuroinvasion in gene-targeted mice expressing cervid S138N prion proteinMaria Immaculata Arifin, Samia Hannaoui, Raychal Ashlyn Ng, et al.Pageof 3