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Items: 28

1.

Correlation between Bioassay and Protein Misfolding Cyclic Amplification for Variant Creutzfeldt-Jakob Disease Decontamination Studies.

Bélondrade M, Jas-Duval C, Nicot S, Bruyère-Ostells L, Mayran C, Herzog L, Reine F, Torres JM, Fournier-Wirth C, Béringue V, Lehmann S, Bougard D.

mSphere. 2020 Jan 29;5(1). pii: e00649-19. doi: 10.1128/mSphere.00649-19.

2.

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

Igel-Egalon A, Laferrière F, Moudjou M, Bohl J, Mezache M, Knäpple T, Herzog L, Reine F, Jas-Duval C, Doumic M, Rezaei H, Béringue V.

Commun Biol. 2019 Oct 4;2:363. doi: 10.1038/s42003-019-0608-y. eCollection 2019.

3.

Prion strain-dependent tropism is maintained between spleen and granuloma and relies on lymphofollicular structures.

Al-Dybiat I, Moudjou M, Martin D, Reine F, Herzog L, Truchet S, Berthon P, Laude H, Rezaei H, Andréoletti O, Béringue V, Sibille P.

Sci Rep. 2019 Oct 10;9(1):14656. doi: 10.1038/s41598-019-51084-1.

4.

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

Igel-Egalon A, Bohl J, Moudjou M, Herzog L, Reine F, Rezaei H, Béringue V.

Viruses. 2019 May 10;11(5). pii: E429. doi: 10.3390/v11050429. Review.

5.

Epigenetic Control of the Notch and Eph Signaling Pathways by the Prion Protein: Implications for Prion Diseases.

Hirsch TZ, Martin-Lannerée S, Reine F, Hernandez-Rapp J, Herzog L, Dron M, Privat N, Passet B, Halliez S, Villa-Diaz A, Lacroux C, Klein V, Haïk S, Andréoletti O, Torres JM, Vilotte JL, Béringue V, Mouillet-Richard S.

Mol Neurobiol. 2019 Mar;56(3):2159-2173. doi: 10.1007/s12035-018-1193-7. Epub 2018 Jul 11.

PMID:
29998397
6.

Reversible unfolding of infectious prion assemblies reveals the existence of an oligomeric elementary brick.

Igel-Egalon A, Moudjou M, Martin D, Busley A, Knäpple T, Herzog L, Reine F, Lepejova N, Richard CA, Béringue V, Rezaei H.

PLoS Pathog. 2017 Sep 7;13(9):e1006557. doi: 10.1371/journal.ppat.1006557. eCollection 2017 Sep.

7.

A stretch of residues within the protease-resistant core is not necessary for prion structure and infectivity.

Munoz-Montesino C, Sizun C, Moudjou M, Herzog L, Reine F, Igel-Egalon A, Barbereau C, Chapuis J, Ciric D, Laude H, Béringue V, Rezaei H, Dron M.

Prion. 2017 Jan 2;11(1):25-30. doi: 10.1080/19336896.2016.1274851. Epub 2017 Feb 8.

8.

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

Le Dur A, Laï TL, Stinnakre MG, Laisné A, Chenais N, Rakotobe S, Passet B, Reine F, Soulier S, Herzog L, Tilly G, Rézaei H, Béringue V, Vilotte JL, Laude H.

Nat Commun. 2017 Jan 23;8:14170. doi: 10.1038/ncomms14170.

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.

Jaumain E, Quadrio I, Herzog L, Reine F, Rezaei H, Andréoletti O, Laude H, Perret-Liaudet A, Haïk S, Béringue V.

J Virol. 2016 Nov 14;90(23):10867-10874. doi: 10.1128/JVI.01383-16. Print 2016 Dec 1.

10.

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

Moudjou M, Chapuis J, Mekrouti M, Reine F, Herzog L, Sibille P, Laude H, Vilette D, Andréoletti O, Rezaei H, Dron M, Béringue V.

Sci Rep. 2016 Jul 7;6:29116. doi: 10.1038/srep29116.

11.

Generating Bona Fide Mammalian Prions with Internal Deletions.

Munoz-Montesino C, Sizun C, Moudjou M, Herzog L, Reine F, Chapuis J, Ciric D, Igel-Egalon A, Laude H, Béringue V, Rezaei H, Dron M.

J Virol. 2016 Jul 11;90(15):6963-6975. doi: 10.1128/JVI.00555-16. Print 2016 Aug 1.

12.

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

Chapuis J, Moudjou M, Reine F, Herzog L, Jaumain E, Chapuis C, Quadrio I, Boulliat J, Perret-Liaudet A, Dron M, Laude H, Rezaei H, Béringue V.

Acta Neuropathol Commun. 2016 Feb 5;4:10. doi: 10.1186/s40478-016-0284-9.

13.

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

Khalifé M, Reine F, Paquet-Fifield S, Castille J, Herzog L, Vilotte M, Moudjou M, Moazami-Goudarzi K, Makhzami S, Passet B, Andréoletti O, Vilette D, Laude H, Béringue V, Vilotte JL.

J Virol. 2015 Nov 25;90(3):1638-46. doi: 10.1128/JVI.02805-15. Print 2016 Feb 1.

14.

Evidence for zoonotic potential of ovine scrapie prions.

Cassard H, Torres JM, Lacroux C, Douet JY, Benestad SL, Lantier F, Lugan S, Lantier I, Costes P, Aron N, Reine F, Herzog L, Espinosa JC, Beringue V, Andréoletti O.

Nat Commun. 2014 Dec 16;5:5821. doi: 10.1038/ncomms6821.

PMID:
25510416
15.

Accelerated, spleen-based titration of variant Creutzfeldt-Jakob disease infectivity in transgenic mice expressing human prion protein with sensitivity comparable to that of survival time bioassay.

Halliez S, Reine F, Herzog L, Jaumain E, Haïk S, Rezaei H, Vilotte JL, Laude H, Béringue V.

J Virol. 2014 Aug;88(15):8678-86. doi: 10.1128/JVI.01118-14. Epub 2014 May 21.

16.

Highly infectious prions generated by a single round of microplate-based protein misfolding cyclic amplification.

Moudjou M, Sibille P, Fichet G, Reine F, Chapuis J, Herzog L, Jaumain E, Laferrière F, Richard CA, Laude H, Andréoletti O, Rezaei H, Béringue V.

mBio. 2013 Dec 31;5(1):e00829-13. doi: 10.1128/mBio.00829-13.

17.

Quaternary structure of pathological prion protein as a determining factor of strain-specific prion replication dynamics.

Laferrière F, Tixador P, Moudjou M, Chapuis J, Sibille P, Herzog L, Reine F, Jaumain E, Laude H, Rezaei H, Béringue V.

PLoS Pathog. 2013;9(10):e1003702. doi: 10.1371/journal.ppat.1003702. Epub 2013 Oct 10.

18.

Facilitated cross-species transmission of prions in extraneural tissue.

Béringue V, Herzog L, Jaumain E, Reine F, Sibille P, Le Dur A, Vilotte JL, Laude H.

Science. 2012 Jan 27;335(6067):472-5. doi: 10.1126/science.1215659.

19.

LIPH expression in skin and hair follicles of normal coat and Rex rabbits.

Diribarne M, Mata X, Rivière J, Bouet S, Vaiman A, Chapuis J, Reine F, Fleurot R, Auvinet G, Deretz S, Allain D, Schibler L, Cribiu EP, Guérin G.

PLoS One. 2012;7(1):e30073. doi: 10.1371/journal.pone.0030073. Epub 2012 Jan 17.

20.

Sheep and goat BSE propagate more efficiently than cattle BSE in human PrP transgenic mice.

Padilla D, Béringue V, Espinosa JC, Andreoletti O, Jaumain E, Reine F, Herzog L, Gutierrez-Adan A, Pintado B, Laude H, Torres JM.

PLoS Pathog. 2011 Mar;7(3):e1001319. doi: 10.1371/journal.ppat.1001319. Epub 2011 Mar 17.

21.

The physical relationship between infectivity and prion protein aggregates is strain-dependent.

Tixador P, Herzog L, Reine F, Jaumain E, Chapuis J, Le Dur A, Laude H, Béringue V.

PLoS Pathog. 2010 Apr 15;6(4):e1000859. doi: 10.1371/journal.ppat.1000859.

22.

Transmission of atypical bovine prions to mice transgenic for human prion protein.

Béringue V, Herzog L, Reine F, Le Dur A, Casalone C, Vilotte JL, Laude H.

Emerg Infect Dis. 2008 Dec;14(12):1898-901. doi: 10.3201/eid1412.080941.

23.

Prominent and persistent extraneural infection in human PrP transgenic mice infected with variant CJD.

Béringue V, Le Dur A, Tixador P, Reine F, Lepourry L, Perret-Liaudet A, Haïk S, Vilotte JL, Fontés M, Laude H.

PLoS One. 2008 Jan 9;3(1):e1419. doi: 10.1371/journal.pone.0001419.

24.

A bovine prion acquires an epidemic bovine spongiform encephalopathy strain-like phenotype on interspecies transmission.

Béringue V, Andréoletti O, Le Dur A, Essalmani R, Vilotte JL, Lacroux C, Reine F, Herzog L, Biacabé AG, Baron T, Caramelli M, Casalone C, Laude H.

J Neurosci. 2007 Jun 27;27(26):6965-71.

25.

Isolation from cattle of a prion strain distinct from that causing bovine spongiform encephalopathy.

Béringue V, Bencsik A, Le Dur A, Reine F, Laï TL, Chenais N, Tilly G, Biacabé AG, Baron T, Vilotte JL, Laude H.

PLoS Pathog. 2006 Oct;2(10):e112.

26.

Detection of a raft-located estrogen receptor-like protein distinct from ER alpha.

Heberden C, Reine F, Grosse B, Henry C, Zagar Y, Chaumaz G, Lieberherr M.

Int J Biochem Cell Biol. 2006 Mar;38(3):376-91. Epub 2005 Oct 3.

PMID:
16263324
27.

A newly identified type of scrapie agent can naturally infect sheep with resistant PrP genotypes.

Le Dur A, Béringue V, Andréoletti O, Reine F, Laï TL, Baron T, Bratberg B, Vilotte JL, Sarradin P, Benestad SL, Laude H.

Proc Natl Acad Sci U S A. 2005 Nov 1;102(44):16031-6. Epub 2005 Oct 20.

28.

Conservation of the prion properties of Ure2p through evolution.

Baudin-Baillieu A, Fernandez-Bellot E, Reine F, Coissac E, Cullin C.

Mol Biol Cell. 2003 Aug;14(8):3449-58. Epub 2003 May 18.

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