Articles citing this article

The Citing articles tool gives a list of articles citing the current article.
The citing articles come from EDP Sciences database, as well as other publishers participating in CrossRef Cited-by Linking Program. You can set up your personal account to receive an email alert each time this article is cited by a new article (see the menu on the right-hand side of the abstract page).

Cited article:

The dynamics of prion spreading is governed by the interplay between the non-linearities of tissue response and replication kinetics

Basile Fornara, Angélique Igel, Vincent Béringue, Davy Martin, Pierre Sibille, Laurent Pujo-Menjouet and Human Rezaei
iScience 27 (12) 111381 (2024)
https://doi.org/10.1016/j.isci.2024.111381

Species barrier as molecular basis for adaptation of synthetic prions with N‐terminally truncated PrP

Human Rezaei, Davy Martin, Laetitia Herzog, Fabienne Reine, Alba Marín Moreno, Mohammed Moudjou, Naima Aron, Angélique Igel, Hannah Klute, Stella Youssafi, Jean‐Baptiste Moog, Pierre Sibille, Olivier Andréoletti, Joan Torrent and Vincent Béringue
The FEBS Journal 291 (22) 5051 (2024)
https://doi.org/10.1111/febs.17291

Transmission of Norwegian reindeer CWD to sheep by intracerebral inoculation results in an unusual phenotype and prion distribution

Erez Harpaz, Federico Angelo Cazzaniga, Linh Tran, Tram T. Vuong, Giuseppe Bufano, Øyvind Salvesen, Maiken Gravdal, Devin Aldaz, Julianna Sun, Sehun Kim, Luigi Celauro, Giuseppe Legname, Glenn C. Telling, Michael A. Tranulis, Sylvie L. Benestad, Arild Espenes, Fabio Moda and Cecilie Ersdal
Veterinary Research 55 (1) (2024)
https://doi.org/10.1186/s13567-024-01350-6

Characterisation of European Field Goat Prion Isolates in Ovine PrP Overexpressing Transgenic Mice (Tgshp IX) Reveals Distinct Prion Strains

Sonja Ernst, Romolo Nonno, Jan Langeveld, Olivier Andreoletti, Cristina Acin, Penelope Papasavva-Stylianou, Theodoros Sklaviadis, Pier Luigi Acutis, Lucien van Keulen, John Spiropoulos, Markus Keller, Martin H. Groschup and Christine Fast
Pathogens 13 (8) 629 (2024)
https://doi.org/10.3390/pathogens13080629

Transgenic Mouse Models for the Study of Neurodegenerative Diseases

Alba Marín-Moreno, Sara Canoyra, Natalia Fernández-Borges, Juan Carlos Espinosa and Juan María Torres
Frontiers in Bioscience-Landmark 28 (1) (2023)
https://doi.org/10.31083/j.fbl2801021

Characterization of the First Case of Classical Scrapie in a Sheep in Tunisia

Abdelkader Amara, Kéfia Elmehatli, Michele Angelo Di Bari, Laura Pirisinu, Rihab Andolsi, Souhir Gachout, Boubaker Ben Smida, Meriem Handous, Heni Haj Ammar, Roukaya Khorchani, Malek Zrelli, Barbara Iulini, Caterina Lucia Florio, Maria Caramelli, Cristina Casalone, Laura De Antoniis, Geraldina Riccardi, Elena Esposito, Matteo Giovannelli, Claudia D’Agostino, Barbara Chiappini, Romolo Nonno, Umberto Agrimi, Gabriele Vaccari and Daniel Diaz
Transboundary and Emerging Diseases 2023 1 (2023)
https://doi.org/10.1155/2023/2253316

Conventional and State-of-the-Art Detection Methods of Bovine Spongiform Encephalopathy (BSE)

Monika Olech
International Journal of Molecular Sciences 24 (8) 7135 (2023)
https://doi.org/10.3390/ijms24087135

Prion assemblies: structural heterogeneity, mechanisms of formation, and role in species barrier

Angélique Igel, Basile Fornara, Human Rezaei and Vincent Béringue
Cell and Tissue Research 392 (1) 149 (2023)
https://doi.org/10.1007/s00441-022-03700-2

Inter- and intra-species conversion efficacies of Norwegian prion isolates estimated by serial protein misfolding cyclic amplification

Erez Harpaz, Tram Thu Vuong, Linh Tran, Michael Andreas Tranulis, Sylvie L. Benestad and Cecilie Ersdal
Veterinary Research 54 (1) (2023)
https://doi.org/10.1186/s13567-023-01220-7

The Smallest Infectious Substructure Encoding the Prion Strain Structural Determinant Revealed by Spontaneous Dissociation of Misfolded Prion Protein Assemblies

Jan Bohl, Mohammed Moudjou, Laetitia Herzog, Fabienne Reine, Fiona Sailer, Hannah Klute, Frederic Halgand, Guillaume Van der Rest, Yves Boulard, Vincent Béringue, Angelique Igel and Human Rezaei
Journal of Molecular Biology 435 (21) 168280 (2023)
https://doi.org/10.1016/j.jmb.2023.168280

Recombinant ovine prion protein can be mutated at position 136 to improve its efficacy as an inhibitor of prion propagation

Katarzyna Kopycka, Ben C. Maddison and Kevin C. Gough
Scientific Reports 13 (1) (2023)
https://doi.org/10.1038/s41598-023-30202-0

Human Rezaei, Davy Martin, Laetitia Herzog, Fabienne Reine, Naima Aron, Angélique Igel, Hannah Klute, Stella Youssafi, Jean-Baptiste Moog, Pierre Sibille, Olivier Andréoletti, Joan Torrent and Vincent Béringue
(2023)
https://doi.org/10.1101/2023.02.27.530231

Jan Bohl, Mohammed Moudjou, Laetitia Herzog, Fabienne Reine, Fiona Sailler, Hannah Klute, Frederic Halgand, Guillaume Van der Rest, Yves Boulard, Vincent Béringue, Angelique Igel and Human Rezaei
(2023)
https://doi.org/10.1101/2023.03.21.533631

Overexpression of mouse prion protein in transgenic mice causes a non-transmissible spongiform encephalopathy

Graham S. Jackson, Jacqueline Linehan, Sebastian Brandner, et al.
Scientific Reports 12 (1) (2022)
https://doi.org/10.1038/s41598-022-21608-3

Strain Typing of Classical Scrapie and Bovine Spongiform Encephalopathy (BSE) by Using Ovine PrP (ARQ/ARQ) Overexpressing Transgenic Mice

Olanrewaju I. Fatola, Markus Keller, Anne Balkema-Buschmann, James Olopade, Martin H. Groschup and Christine Fast
International Journal of Molecular Sciences 23 (12) 6744 (2022)
https://doi.org/10.3390/ijms23126744

Variation in the PRNP gene of Pere David’s deer (Elaphurus davidianus) may impact genetic vulnerability to chronic wasting disease

Tolulope I. N. Perrin-Stowe, Yasuko Ishida, Emily E. Terrill, et al.
Conservation Genetics 23 (2) 313 (2022)
https://doi.org/10.1007/s10592-021-01419-1

Aged Cattle Brain Displays Alzheimer's Disease-Like Pathology and Promotes Brain Amyloidosis in a Transgenic Animal Model

Ines Moreno-Gonzalez, George Edwards, Rodrigo Morales, et al.
Frontiers in Aging Neuroscience 13 (2022)
https://doi.org/10.3389/fnagi.2021.815361

Porcine Prion Protein as a Paradigm of Limited Susceptibility to Prion Strain Propagation

Juan Carlos Espinosa, Alba Marín-Moreno, Patricia Aguilar-Calvo, et al.
The Journal of Infectious Diseases 223 (6) 1103 (2021)
https://doi.org/10.1093/infdis/jiz646

Differential Accumulation of Misfolded Prion Strains in Natural Hosts of Prion Diseases

Zoe J. Lambert, Justin J. Greenlee, Eric D. Cassmann and M. Heather West Greenlee
Viruses 13 (12) 2453 (2021)
https://doi.org/10.3390/v13122453

Review on PRNP genetics and susceptibility to chronic wasting disease of Cervidae

Katayoun Moazami-Goudarzi, Olivier Andréoletti, Jean-Luc Vilotte and Vincent Béringue
Veterinary Research 52 (1) (2021)
https://doi.org/10.1186/s13567-021-00993-z

Met166‐Glu168 residues in human PrP β2‐α2 loop account for evolutionary resistance to prion infection

Juan Carlos Espinosa, Alba Marín‐Moreno, Patricia Aguilar‐Calvo and Juan María Torres
Neuropathology and Applied Neurobiology 47 (4) 506 (2021)
https://doi.org/10.1111/nan.12676

Allelic Interference in Prion Replication Is Modulated by the Convertibility of the Interfering PrP C and Other Host-Specific Factors

Juan Carlos Espinosa, Olivier Andreoletti, Alba Marín-Moreno, et al.
mBio 12 (2) (2021)
https://doi.org/10.1128/mBio.03508-20

Interventions to reduce the risk of surgically transmitted Creutzfeldt–Jakob disease: a cost-effective modelling review

Matt Stevenson, Lesley Uttley, Jeremy E Oakley, et al.
Health Technology Assessment 24 (11) 1 (2020)
https://doi.org/10.3310/hta24110

Improving the Predictive Value of Prion Inactivation Validation Methods to Minimize the Risks of Iatrogenic Transmission With Medical Instruments

Mohammed Moudjou, Johan Castille, Bruno Passet, et al.
Frontiers in Bioengineering and Biotechnology 8 (2020)
https://doi.org/10.3389/fbioe.2020.591024

Host prion protein expression levels impact prion tropism for the spleen

Vincent Béringue, Philippe Tixador, Olivier Andréoletti, et al.
PLOS Pathogens 16 (7) e1008283 (2020)
https://doi.org/10.1371/journal.ppat.1008283

Mixtures of prion substrains in natural scrapie cases revealed by ovinised murine models

Tomás Barrio, Hicham Filali, Alicia Otero, et al.
Scientific Reports 10 (1) (2020)
https://doi.org/10.1038/s41598-020-61977-1

Prions and Neurodegenerative Diseases

Alba Marín-Moreno, Juan Carlos Espinosa and Juan María Torres
Progress in Molecular Biology and Translational Science, Prions and Neurodegenerative Diseases 175 147 (2020)
https://doi.org/10.1016/bs.pmbts.2020.08.007

Prions and Neurodegenerative Diseases

L. McAlary, J.J. Yerbury and N.R. Cashman
Progress in Molecular Biology and Translational Science, Prions and Neurodegenerative Diseases 175 261 (2020)
https://doi.org/10.1016/bs.pmbts.2020.07.002

Prions from Sporadic Creutzfeldt-Jakob Disease Patients Propagate as Strain Mixtures

Hervé Cassard, Alvina Huor, Juan-Carlos Espinosa, et al.
mBio 11 (3) (2020)
https://doi.org/10.1128/mBio.00393-20

Re-transmissibility of mouse-adapted ME7 scrapie strain to ovine PrP transgenic mice

Joshua Adekunle Babalola, Jong-Mu Kim, Yun-Jung Lee, et al.
Journal of Veterinary Science 20 (2) (2019)
https://doi.org/10.4142/jvs.2019.20.e8

Transition of the prion protein from a structured cellular form (PrPC) to the infectious scrapie agent (PrPSc)

Pravas K. Baral, Jiang Yin, Adriano Aguzzi and Michael N. G. James
Protein Science 28 (12) 2055 (2019)
https://doi.org/10.1002/pro.3735

Nucleotide structure of prion protein gene in Egyptian camels

Sekena H. Abdel-Aziem, Heba A. M. Abd El-Kader, Sally S. Alam, Omaima M. Abd El-Moneim and Othman E. Othman
Journal of Applied Animal Research 47 (1) 123 (2019)
https://doi.org/10.1080/09712119.2019.1580584

Early stage prion assembly involves two subpopulations with different quaternary structures and a secondary templating pathway

Angélique Igel-Egalon, Florent Laferrière, Mohammed Moudjou, et al.
Communications Biology 2 (1) (2019)
https://doi.org/10.1038/s42003-019-0608-y

The emergence of classical BSE from atypical/Nor98 scrapie

Alvina Huor, Juan Carlos Espinosa, Enric Vidal, et al.
Proceedings of the National Academy of Sciences 116 (52) 26853 (2019)
https://doi.org/10.1073/pnas.1915737116

Vincent Béringue, Philippe Tixador, Olivier Andréoletti, Fabienne Reine, Johan Castille, Thanh-Lan Laï, Annick Le Dur, Aude Laisné, Laetitia Herzog, Bruno Passet, Human Rezaei, Jean-Luc Vilotte and Hubert Laude
(2019)
https://doi.org/10.1101/2019.12.17.879676

Heterogeneity and Architecture of Pathological Prion Protein Assemblies: Time to Revisit the Molecular Basis of the Prion Replication Process?

Angélique Igel-Egalon, Jan Bohl, Mohammed Moudjou, Laetitia Herzog, Fabienne Reine, Human Rezaei and Vincent Béringue
Viruses 11 (5) 429 (2019)
https://doi.org/10.3390/v11050429

Angélique Igel-Egalon, Florent Laferrière, Philippe Tixador, Mohammed Moudjou, Laetitia Herzog, Fabienne Reine, Juan Maria Torres, Hubert Laude, Human Rezaei and Vincent Béringue
(2019)
https://doi.org/10.1101/861278

Use of different RT-QuIC substrates for detecting CWD prions in the brain of Norwegian cervids

Edoardo Bistaffa, Tram Thu Vuong, Federico Angelo Cazzaniga, et al.
Scientific Reports 9 (1) (2019)
https://doi.org/10.1038/s41598-019-55078-x

Angélique Igel-Egalon, Florent Laferrière, Mohammed Moudjou, Mathieu Merzach, Tina Knäpple, Laetitia Herzog, Fabienne Reine, Marie Doumic, Human Rezaei and Vincent Béringue
(2019)
https://doi.org/10.1101/583781

Presumptive BSE cases with an aberrant prion protein phenotype in Switzerland, 2011: Lack of prion disease in experimentally inoculated cattle and bovine prion protein transgenic mice

F. Serra, S. Dudas, J. M. Torres, et al.
Transboundary and Emerging Diseases 65 (5) 1348 (2018)
https://doi.org/10.1111/tbed.12884

Prion replication environment defines the fate of prion strain adaptation

Elizaveta Katorcha, Nuria Gonzalez-Montalban, Natallia Makarava, et al.
PLOS Pathogens 14 (6) e1007093 (2018)
https://doi.org/10.1371/journal.ppat.1007093

Current evidence on the transmissibility of chronic wasting disease prions to humans-A systematic review

L. Waddell, J. Greig, M. Mascarenhas, et al.
Transboundary and Emerging Diseases 65 (1) 37 (2018)
https://doi.org/10.1111/tbed.12612

Experimental sheep BSE prions generate the vCJD phenotype when serially passaged in transgenic mice expressing human prion protein

Susan Joiner, Emmanuel A. Asante, Jacqueline M. Linehan, et al.
Journal of the Neurological Sciences 386 4 (2018)
https://doi.org/10.1016/j.jns.2017.12.038

Nonpathogenic Heterologous Prions Can Interfere with Prion Infection in a Strain-Dependent Manner

Alba Marín-Moreno, Patricia Aguilar-Calvo, José Luis Pitarch, et al.
Journal of Virology 92 (24) (2018)
https://doi.org/10.1128/JVI.01086-18

Biomolecular Assemblies: Moving from Observation to Predictive Design

Corey J. Wilson, Andreas S. Bommarius, Julie A. Champion, et al.
Chemical Reviews 118 (24) 11519 (2018)
https://doi.org/10.1021/acs.chemrev.8b00038

Protein Misfolding Cyclic Amplification Cross-Species Products of Mouse-Adapted Scrapie Strain 139A and Hamster-Adapted Scrapie Strain 263K with Brain and Muscle Tissues of Opposite Animals Generate Infectious Prions

Chen Gao, Jun Han, Jin Zhang, et al.
Molecular Neurobiology 54 (5) 3771 (2017)
https://doi.org/10.1007/s12035-016-9945-8

Divergent prion strain evolution driven by PrPC expression level in transgenic mice

Annick Le Dur, Thanh Lan Laï, Marie-George Stinnakre, et al.
Nature Communications 8 (1) (2017)
https://doi.org/10.1038/ncomms14170

Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells

Kohtaro Miyazawa, Kentaro Masujin, Hiroyuki Okada, et al.
PLOS ONE 12 (6) e0179317 (2017)
https://doi.org/10.1371/journal.pone.0179317

Amyloid formation characteristics of GNNQQNY from yeast prion protein Sup35 and its seeding with heterogeneous polypeptides

Mamoru Haratake, Tohru Takiguchi, Naho Masuda, et al.
Colloids and Surfaces B: Biointerfaces 149 72 (2017)
https://doi.org/10.1016/j.colsurfb.2016.10.011

Experimental Infection of Cattle With a Novel Prion Derived From Atypical H-Type Bovine Spongiform Encephalopathy

Hiroyuki Okada, Kentaro Masujin, Kohtaro Miyazawa, Yoshifumi Iwamaru, Morikazu Imamura, Yuichi Matsuura, Shozo Arai, Shigeo Fukuda, Yuichi Murayama and Takashi Yokoyama
Veterinary Pathology 54 (6) 892 (2017)
https://doi.org/10.1177/0300985817717769

Mutated but Not Deleted Ovine PrP C N-Terminal Polybasic Region Strongly Interferes with Prion Propagation in Transgenic Mice

Manal Khalifé, Fabienne Reine, Sophie Paquet-Fifield, et al.
Journal of Virology 90 (3) 1638 (2016)
https://doi.org/10.1128/JVI.02805-15

Glycoform-independent prion conversion by highly efficient, cell-based, protein misfolding cyclic amplification

Mohammed Moudjou, Jérôme Chapuis, Mériem Mekrouti, et al.
Scientific Reports 6 (1) (2016)
https://doi.org/10.1038/srep29116

Emergence of two prion subtypes in ovine PrP transgenic mice infected with human MM2-cortical Creutzfeldt-Jakob disease prions

Jérôme Chapuis, Mohammed Moudjou, Fabienne Reine, et al.
Acta Neuropathologica Communications 4 (1) (2016)
https://doi.org/10.1186/s40478-016-0284-9

Absence of Evidence for a Causal Link between Bovine Spongiform Encephalopathy Strain Variant L-BSE and Known Forms of Sporadic Creutzfeldt-Jakob Disease in Human PrP Transgenic Mice

Emilie Jaumain, Isabelle Quadrio, Laetitia Herzog, et al.
Journal of Virology 90 (23) 10867 (2016)
https://doi.org/10.1128/JVI.01383-16

Generating Bona Fide Mammalian Prions with Internal Deletions

Carola Munoz-Montesino, Christina Sizun, Mohammed Moudjou, et al.
Journal of Virology 90 (15) 6963 (2016)
https://doi.org/10.1128/JVI.00555-16

The role of the unusual threonine string in the conversion of prion protein

Romany Abskharon, Fei Wang, Kayla J. Vander Stel, Kumar Sinniah and Jiyan Ma
Scientific Reports 6 (1) (2016)
https://doi.org/10.1038/srep38877

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

Eirini Kanata, Minas Arsenakis and Theodoros Sklaviadis
Prion 10 (5) 391 (2016)
https://doi.org/10.1080/19336896.2016.1199312

Generic amyloidogenicity of mammalian prion proteins from species susceptible and resistant to prions

Sofie Nyström and Per Hammarström
Scientific Reports 5 (1) (2015)
https://doi.org/10.1038/srep10101

Acquired transmissibility of sheep-passaged L-type bovine spongiform encephalopathy prion to wild-type mice

Hiroyuki Okada, Kentaro Masujin, Kohtaro Miyazawa and Takashi Yokoyama
Veterinary Research 46 (1) (2015)
https://doi.org/10.1186/s13567-015-0211-2

Effect of Q211and K222PRNPPolymorphic Variants in the Susceptibility of Goats to Oral Infection With Goat Bovine Spongiform Encephalopathy

Patricia Aguilar-Calvo, Christine Fast, Kerstin Tauscher, et al.
Journal of Infectious Diseases 212 (4) 664 (2015)
https://doi.org/10.1093/infdis/jiv112

Prion protein (PrP) gene-knockout cell lines: insight into functions of the PrP

Akikazu Sakudo and Takashi Onodera
Frontiers in Cell and Developmental Biology 2 (2015)
https://doi.org/10.3389/fcell.2014.00075

Prion strains are differentially released through the exosomal pathway

Zaira E. Arellano-Anaya, Alvina Huor, Pascal Leblanc, et al.
Cellular and Molecular Life Sciences 72 (6) 1185 (2015)
https://doi.org/10.1007/s00018-014-1735-8

Genetic and Pathological Follow-Up Study of Goats Experimentally and Naturally Exposed to a Sheep Scrapie Isolate

Caterina Maestrale, Maria G. Cancedda, Davide Pintus, et al.
Journal of Virology 89 (19) 10044 (2015)
https://doi.org/10.1128/JVI.01262-15

Signal Transduction by a Fungal NOD-Like Receptor Based on Propagation of a Prion Amyloid Fold

Asen Daskalov, Birgit Habenstein, Denis Martinez, et al.
PLOS Biology 13 (2) e1002059 (2015)
https://doi.org/10.1371/journal.pbio.1002059

X-ray structural and molecular dynamical studies of the globular domains of cow, deer, elk and Syrian hamster prion proteins

Pravas Kumar Baral, Mridula Swayampakula, Adriano Aguzzi and Michael N.G. James
Journal of Structural Biology 192 (1) 37 (2015)
https://doi.org/10.1016/j.jsb.2015.08.014

The Glycosylation Status of PrP C Is a Key Factor in Determining Transmissible Spongiform Encephalopathy Transmission between Species

Frances K. Wiseman, Enrico Cancellotti, Pedro Piccardo, et al.
Journal of Virology 89 (9) 4738 (2015)
https://doi.org/10.1128/JVI.02296-14

W8, a new Sup35 prion strain, transmits distinctive information with a conserved assembly scheme

Yu-Wen Huang, Yuan-Chih Chang, Ruben Diaz-Avalos and Chih-Yen King
Prion 9 (3) 207 (2015)
https://doi.org/10.1080/19336896.2015.1039217

Did the prion protein become vulnerable to misfolding after an evolutionary divide and conquer event?

Kacy Richmond, Patrick Masterson, Juan Felipe Ortiz and Jessica Siltberg-Liberles
Journal of Biomolecular Structure and Dynamics 32 (7) 1074 (2014)
https://doi.org/10.1080/07391102.2013.809022

Genetic Resistance to Scrapie Infection in Experimentally Challenged Goats

Caroline Lacroux, Cécile Perrin-Chauvineau, Fabien Corbière, et al.
Journal of Virology 88 (5) 2406 (2014)
https://doi.org/10.1128/JVI.02872-13

PrP Expression Level and Sensitivity to Prion Infection

Jean-Yves Douet, Caroline Lacroux, Fabien Corbière, et al.
Journal of Virology 88 (10) 5870 (2014)
https://doi.org/10.1128/JVI.00369-14

Evidence for zoonotic potential of ovine scrapie prions

Hervé Cassard, Juan-Maria Torres, Caroline Lacroux, et al.
Nature Communications 5 (1) (2014)
https://doi.org/10.1038/ncomms6821