Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Jean-Marc Bilheude"'
Autor:
Stéphanie Simon, Jérôme Nugier, Nathalie Morel, Hervé Boutal, Christophe Créminon, Sylvie L. Benestad, Olivier Andréoletti, Frédéric Lantier, Jean-Marc Bilheude, Muriel Feyssaguet, Anne-Gaëlle Biacabe, Thierry Baron, Jacques Grassi
Publikováno v:
Emerging Infectious Diseases, Vol 14, Iss 4, Pp 608-616 (2008)
The bovine spongiform encephalopathy (BSE) agent has been transmitted to humans, leading to variant Creutzfeldt-Jakob disease. Sheep and goats can be experimentally infected by BSE and have been potentially exposed to natural BSE; however, whether BS
Externí odkaz:
https://doaj.org/article/49b03365c3be4da2a5de46d9d8d7a5c1
Autor:
Emmanuelle Uro-Coste, Hervé Cassard, Stéphanie Simon, Séverine Lugan, Jean-Marc Bilheude, Armand Perret-Liaudet, James W Ironside, Stéphane Haik, Christelle Basset-Leobon, Caroline Lacroux, Katell Peoch', Nathalie Streichenberger, Jan Langeveld, Mark W Head, Jacques Grassi, Jean-Jacques Hauw, Francois Schelcher, Marie Bernadette Delisle, Olivier Andréoletti
Publikováno v:
PLoS Pathogens, Vol 4, Iss 3, p e1000029 (2008)
Sporadic Creutzfeldt-Jakob disease (sCJD) cases are currently subclassified according to the methionine/valine polymorphism at codon 129 of the PRNP gene and the proteinase K (PK) digested abnormal prion protein (PrP(res)) identified on Western blott
Externí odkaz:
https://doaj.org/article/b4b622169ff8416bb3e11fae5b8545c4
Autor:
Jean-Noël Arsac, Olivier Andreoletti, Jean-Marc Bilheude, Caroline Lacroux, Sylvie L. Benestad, Thierry G.M. Baron
Publikováno v:
Emerging Infectious Diseases, Vol 13, Iss 1, Pp 58-58 (2007)
Isolates of atypical scrapie recently identified in sheep and goats in France were compared with Nor98 isolates reported in Norway. Western blot methods for characterization of the protease-resistant prion protein showed that all these isolates share
Externí odkaz:
https://doaj.org/article/aecee1e57980475ea00975bc04b54c43
Autor:
Emmanuelle, Uro-Coste, Hervé, Cassard, Stéphanie, Simon, Séverine, Lugan, Jean-Marc, Bilheude, Armand, Perret-Liaudet, James W, Ironside, Stéphane, Haik, Christelle, Basset-Leobon, Caroline, Lacroux, Katell, Peoch, Nathalie, Streichenberger, Jan, Langeveld, Mark W, Head, Jacques, Grassi, Jean-Jacques, Hauw, Francois, Schelcher, Marie Bernadette, Delisle, Olivier, Andréoletti
Publikováno v:
PLoS pathogens. 4(3)
Sporadic Creutzfeldt-Jakob disease (sCJD) cases are currently subclassified according to the methionine/valine polymorphism at codon 129 of the PRNP gene and the proteinase K (PK) digested abnormal prion protein (PrPres)identified on Western blotting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5a4e795f2e720640d7d2307943bca263
https://pubmed.ncbi.nlm.nih.gov/18383623
https://pubmed.ncbi.nlm.nih.gov/18383623
Autor:
Muriel Feyssaguet, Nathalie Morel, Jean-Marc Bilheude, Hervé Boutal, Jacques Grassi, Jérôme Nugier, Christophe Créminon, Stéphanie Simon, Olivier Andreoletti, Sylvie L. Benestad, Frédéric Lantier, Anne-Gaëlle Biacabe, Thierry Baron
Publikováno v:
Emerging Infectious Diseases
Emerging Infectious Diseases, 2008, 14 (4), pp.608-16
Emerging Infectious Diseases, Centers for Disease Control and Prevention, 2008, 14 (4), pp.608-16
HAL
Emerging Infectious Diseases, Vol 14, Iss 4, Pp 608-616 (2008)
Emerging Infectious Diseases 4 (14), 608-16. (2008)
Emerging Infectious Diseases, 2008, 14 (4), pp.608-16
Emerging Infectious Diseases, Centers for Disease Control and Prevention, 2008, 14 (4), pp.608-16
HAL
Emerging Infectious Diseases, Vol 14, Iss 4, Pp 608-616 (2008)
Emerging Infectious Diseases 4 (14), 608-16. (2008)
A strain-typing ELISA distinguishes bovine spongiform encephalopathy from other scrapie strains in small ruminants.
The bovine spongiform encephalopathy (BSE) agent has been transmitted to humans, leading to variant Creutzfeldt-Jakob disease. Sh
The bovine spongiform encephalopathy (BSE) agent has been transmitted to humans, leading to variant Creutzfeldt-Jakob disease. Sh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc835b9474bf2d5368261ac80b61f9d7
https://anses.hal.science/hal-00373563
https://anses.hal.science/hal-00373563
Autor:
Marie Bernadette Delisle, Olivier Andreoletti, Jan P. M. Langeveld, Stéphane Haïk, Jean-Marc Bilheude, François Schelcher, Armand Perret-Liaudet, Jean-Jacques Hauw, Nathalie Streichenberger, James W. Ironside, Christelle Basset-Leobon, Caroline Lacroux, Jacques Grassi, Stéphanie Simon, Hervé Cassard, Katell Peoc'h, Séverine Lugan, Mark Head, Emmanuelle Uro-Coste
Publikováno v:
PLoS Pathogens 4 (2008) 3
Plos Pathogens 3 (4), 9 p.. (2008)
PLoS Pathogens, 4(3)
Uro-Coste, E, Cassard, H, Simon, S, Lugan, S, Bilheude, J-M, Perret-Liaudet, A, Ironside, J W, Haik, S, Basset-Leobon, C, Lacroux, C, Peoch, K, Streichenberger, N, Langeveld, J, Head, M W, Grassi, J, Hauw, J-J, Schelcher, F, Delisle, M B & Andréoletti, O 2008, ' Beyond PrP res type 1/type 2 dichotomy in Creutzfeldt-Jakob disease ', PLoS Pathogens, vol. 4, no. 3, pp. e1000029 . https://doi.org/10.1371/journal.ppat.1000029
Plos Pathogens 3 (4), 9 p.. (2008)
PLoS Pathogens, 4(3)
Uro-Coste, E, Cassard, H, Simon, S, Lugan, S, Bilheude, J-M, Perret-Liaudet, A, Ironside, J W, Haik, S, Basset-Leobon, C, Lacroux, C, Peoch, K, Streichenberger, N, Langeveld, J, Head, M W, Grassi, J, Hauw, J-J, Schelcher, F, Delisle, M B & Andréoletti, O 2008, ' Beyond PrP res type 1/type 2 dichotomy in Creutzfeldt-Jakob disease ', PLoS Pathogens, vol. 4, no. 3, pp. e1000029 . https://doi.org/10.1371/journal.ppat.1000029
Sporadic Creutzfeldt-Jakob disease (sCJD) cases are currently subclassified according to the methionine/valine polymorphism at codon 129 of the PRNP gene and the proteinase K (PK) digested abnormal prion protein (PrP(res)) identified on Western blott
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0fefb6a03c15f05f9ab3e6768eba88c
https://research.wur.nl/en/publications/beyond-prpres-type-1type-2-dichotomy-in-creutzfeldt-jakob-disease
https://research.wur.nl/en/publications/beyond-prpres-type-1type-2-dichotomy-in-creutzfeldt-jakob-disease