Citations (31)
Keep up to date with the latest research on this topic with citation updates for this article.
Read on this site (1)
Eirini Kanata, Minas Arsenakis & Theodoros Sklaviadis. (2016) Caprine PrP variants harboring Asp-146, His-154 and Gln-211 alleles display reduced convertibility upon interaction with pathogenic murine prion protein in scrapie infected cells. Prion 10:5, pages 391-408.
Read now
Read now
Articles from other publishers (30)
Katarzyna Kopycka, Ben C. Maddison & Kevin C. Gough. (2023) Recombinant ovine prion protein can be mutated at position 136 to improve its efficacy as an inhibitor of prion propagation. Scientific Reports 13:1.
Crossref
Crossref
Jennifer Myskiw, Lise Lamoureux, Anne Peterson, David Knox, Gerard H. Jansen, Michael B. Coulthart & Stephanie A. Booth. (2023) Development of an Automated Capillary Immunoassay to Detect Prion Glycotypes in Creutzfeldt-Jakob Disease. Laboratory Investigation 103:3, pages 100029.
Crossref
Crossref
Ying-Chiang J. Lee. (2023) Prions: a threat to health security and the need for effective medical countermeasures. Global Health Journal 7:1, pages 43-48.
Crossref
Crossref
Vishruth Mullapudi, Jaime Vaquer-Alicea, Vaibhav Bommareddy, Anthony R. Vega, Bryan D. Ryder, Charles L. WhiteIIIIII, Marc. I. Diamond & Lukasz A. Joachimiak. (2023) Network of hotspot interactions cluster tau amyloid folds. Nature Communications 14:1.
Crossref
Crossref
Shinjinee Sengupta, Shaikh Maryam Ghufran, Aqsa Khan, Subhrajit Biswas & Susanta Roychoudhury. (2022) Transition of amyloid/mutant p53 from tumor suppressor to an oncogene and therapeutic approaches to ameliorate metastasis and cancer stemness. Cancer Cell International 22:1.
Crossref
Crossref
Yingjun Liu, Assunta Senatore, Silvia Sorce, Mario Nuvolone, Jingjing Guo, Zeynep H. Gümüş & Adriano Aguzzi. (2022) Brain aging is faithfully modelled in organotypic brain slices and accelerated by prions. Communications Biology 5:1.
Crossref
Crossref
O. N. Tikhodeyev. (2022) Prions as Non-Canonical Hereditary Factors. Russian Journal of Genetics 58:6, pages 626-637.
Crossref
Crossref
Ivanildo P. SousaJr.Jr., Flavia B. dos Santos, Vanessa S. de Paula, Tuane C.R.G. Vieira, Helver G. Dias, Caroline A. Barros & Edson E. da Silva. (2021) Viral and Prion Infections Associated with Central Nervous System Syndromes in Brazil. Viruses 13:7, pages 1370.
Crossref
Crossref
Maria Immaculata Arifin, Samia Hannaoui, Sheng Chun Chang, Simrika Thapa, Hermann M. Schatzl & Sabine Gilch. (2021) Cervid Prion Protein Polymorphisms: Role in Chronic Wasting Disease Pathogenesis. International Journal of Molecular Sciences 22:5, pages 2271.
Crossref
Crossref
Emily Craven, Martell Winters, Alvin L. Smith, Erin Lalime, Rocco Mancinelli, Brian Shirey, Wayne Schubert, Andrew Schuerger, Mariko Burgin, Emily P. Seto, Morgan Hendry, Amruta Mehta, J. Nick Benardini & Gary Ruvkun. (2021) Biological safety in the context of backward planetary protection and Mars Sample Return: conclusions from the Sterilization Working Group. International Journal of Astrobiology 20:1, pages 1-28.
Crossref
Crossref
Eric Cassmann, Sarah Jo Moore, Robyn Kokemuller, Anne Balkema-Buschmann, Martin Groschup, Eric Nicholson & Justin Greenlee. (2020) Bovine adapted transmissible mink encephalopathy is similar to L-BSE after passage through sheep with the VRQ/VRQ genotype but not VRQ/ARQ. BMC Veterinary Research 16:1.
Crossref
Crossref
Camila Q.M. Bruna, Rafael Queiroz de Souza & Kazuko U. Graziano. (2020)
Review
: Trends in Processing Prion-Contaminated Surgical Instruments
. Biomedical Instrumentation & Technology 54:5, pages 332-337.
Crossref
Crossref
Hailey Pineau & Valerie Sim. (2020) POSCAbilities: The Application of the Prion Organotypic Slice Culture Assay to Neurodegenerative Disease Research. Biomolecules 10:7, pages 1079.
Crossref
Crossref
Surabhi Mehra, Shruti Sahay & Samir K. Maji. (2019) α-Synuclein misfolding and aggregation: Implications in Parkinson’s disease pathogenesis. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics 1867:10, pages 890-908.
Crossref
Crossref
Elisa Meneghetti, Lisa Gasperini, Tommaso Virgilio, Fabio Moda, Fabrizio Tagliavini, Federico Benetti & Giuseppe Legname. (2019) Prions Strongly Reduce NMDA Receptor S-Nitrosylation Levels at Pre-symptomatic and Terminal Stages of Prion Diseases. Molecular Neurobiology 56:9, pages 6035-6045.
Crossref
Crossref
Amberley D. Stephens, Maria Zacharopoulou & Gabriele S. Kaminski Schierle. (2019) The Cellular Environment Affects Monomeric α-Synuclein Structure. Trends in Biochemical Sciences 44:5, pages 453-466.
Crossref
Crossref
Tritia R. Yamasaki, Brandon B. Holmes, Jennifer L. Furman, Dhruva D. Dhavale, Bryant W. Su, Eun-Suk Song, Nigel J. Cairns, Paul T. Kotzbauer & Marc I. Diamond. (2019) Parkinson’s disease and multiple system atrophy have distinct α-synuclein seed characteristics. Journal of Biological Chemistry 294:3, pages 1045-1058.
Crossref
Crossref
Eleanna Kara, Jordan D. Marks & Adriano Aguzzi. (2018) Toxic Protein Spread in Neurodegeneration: Reality versus Fantasy. Trends in Molecular Medicine 24:12, pages 1007-1020.
Crossref
Crossref
Robert Hnasko, Alice Lin, Jeffery McGarvey & Larry Stanker. (2018) Enhanced detection of infectious prions by direct ELISA from the brains of asymptomatic animals using DRM2-118 monoclonal antibody and Gdn-HCl. Journal of Immunological Methods 456, pages 38-43.
Crossref
Crossref
Juan Carlos Polanco, Chuanzhou Li, Liviu-Gabriel Bodea, Ramon Martinez-Marmol, Frederic A. Meunier & Jürgen Götz. (2017) Amyloid-β and tau complexity — towards improved biomarkers and targeted therapies. Nature Reviews Neurology 14:1, pages 22-39.
Crossref
Crossref
Wouter Peelaerts, Veerle Baekelandt & Patrik Brundin. 2018. The Molecular and Cellular Basis of Neurodegenerative Diseases. The Molecular and Cellular Basis of Neurodegenerative Diseases
189
242
.
Qi Shi, Li-Na Chen, Yan Lv, Bao-Yun Zhang, Kang Xiao, Wei Zhou, Cao Chen, Jing Sun, Xiao-Dong Yang & Xiao-Ping Dong. (2017) Comparative proteomics analyses for 139A and ME7 scrapie infected mice brains in the middle and terminal stages. PROTEOMICS - Clinical Applications 11:5-6, pages 1600113.
Crossref
Crossref
Vladimir N. Uversky. (2017) Looking at the recent advances in understanding α-synuclein and its aggregation through the proteoform prism. F1000Research 6, pages 525.
Crossref
Crossref
Wouter Peelaerts & Veerle Baekelandt. (2016) ɑ-Synuclein strains and the variable pathologies of synucleinopathies. Journal of Neurochemistry 139, pages 256-274.
Crossref
Crossref
Bahareh Eftekharzadeh, Bradley T. Hyman & Susanne Wegmann. (2016) Structural studies on the mechanism of protein aggregation in age related neurodegenerative diseases. Mechanisms of Ageing and Development 156, pages 1-13.
Crossref
Crossref
G. Legname & K.E. Pischke. 2016. Encyclopedia of Cell Biology. Encyclopedia of Cell Biology
839
844
.
Susan F. Godsave, Peter J. Peters & Holger Wille. (2015) Subcellular distribution of the prion protein in sickness and in health. Virus Research 207, pages 136-145.
Crossref
Crossref
Sofie Nyström & Per Hammarström. (2015) Generic amyloidogenicity of mammalian prion proteins from species susceptible and resistant to prions. Scientific Reports 5:1.
Crossref
Crossref
QI SHI, KANG XIAO, BAO-YUN ZHANG, XIAO-MEI ZHANG, LI-NA CHEN, CAO CHEN, CHEN GAO & XIAO-PING DONG. (2015) Successive passaging of the scrapie strains, ME7-ha and 139A-ha, generated by the interspecies transmission of mouse-adapted strains into hamsters markedly shortens the incubation times, but maintains their molecular and pathological properties. International Journal of Molecular Medicine 35:4, pages 1138-1146.
Crossref
Crossref
Coralie Pain, Janice Dumont & Mireille Dumoulin. (2015) Camelid single-domain antibody fragments: Uses and prospects to investigate protein misfolding and aggregation, and to treat diseases associated with these phenomena. Biochimie 111, pages 82-106.
Crossref
Crossref