Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Nicole, Salès"'
Autor:
Yervand Eduard Karapetyan, Paula Saá, Sukhvir Paul Mahal, Gian Franco Sferrazza, Alexandra Sherman, Nicole Salès, Charles Weissmann, Corinne Ida Lasmézas
Publikováno v:
PLoS ONE, Vol 4, Iss 5, p e5730 (2009)
Prion strain identification has been hitherto achieved using time-consuming incubation time determinations in one or more mouse lines and elaborate neuropathological assessment. In the present work, we make a detailed study of the properties of PrP-o
Externí odkaz:
https://doaj.org/article/e8cef4a3c83e4f7aacf804fb91c9b123
Autor:
Emmanuel E Comoy, Cristina Casalone, Nathalie Lescoutra-Etchegaray, Gianluigi Zanusso, Sophie Freire, Dominique Marcé, Frédéric Auvré, Marie-Magdeleine Ruchoux, Sergio Ferrari, Salvatore Monaco, Nicole Salès, Maria Caramelli, Philippe Leboulch, Paul Brown, Corinne I Lasmézas, Jean-Philippe Deslys
Publikováno v:
PLoS ONE, Vol 3, Iss 8, p e3017 (2008)
BACKGROUND: Human variant Creutzfeldt-Jakob Disease (vCJD) results from foodborne transmission of prions from slaughtered cattle with classical Bovine Spongiform Encephalopathy (cBSE). Atypical forms of BSE, which remain mostly asymptomatic in aging
Externí odkaz:
https://doaj.org/article/cde7cdfc27f54204bb60506cf5f46bc5
Autor:
Steve Simoneau, Human Rezaei, Nicole Salès, Gunnar Kaiser-Schulz, Maxime Lefebvre-Roque, Catherine Vidal, Jean-Guy Fournier, Julien Comte, Franziska Wopfner, Jeanne Grosclaude, Hermann Schätzl, Corinne Ida Lasmézas
Publikováno v:
PLoS Pathogens, Vol 3, Iss 8, p e125 (2007)
The mechanisms underlying prion-linked neurodegeneration remain to be elucidated, despite several recent advances in this field. Herein, we show that soluble, low molecular weight oligomers of the full-length prion protein (PrP), which possess charac
Externí odkaz:
https://doaj.org/article/b78586e103e84f01b240feec7e8ce3fb
Autor:
Jia Huang, Nicole Salès, Amy J. Ramsey, Mohammad Ali Faghihi, Marc G. Caron, Henrik Frydenlund Hansen, Joacim Elmén, Sakari Kauppinen, Paul J. Kenny, David Willoughby, Miguel A. Lopez-Toledano, Henrik Ørum, Jannet Kocerha, Claes Wahlestedt
Publikováno v:
Proceedings of the National Academy of Sciences. 106:3507-3512
N -methyl- d -aspartate (NMDA) glutamate receptors are regulators of fast neurotransmission and synaptic plasticity in the brain. Disruption of NMDA-mediated glutamate signaling has been linked to behavioral deficits displayed in psychiatric disorder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c24187694f208e0a7f30d097cab81235
https://doi.org/10.1073/pnas.0805854106
https://doi.org/10.1073/pnas.0805854106
Publikováno v:
Journal of Laser Applications. 20:69-75
This study involved the corneal effects of the laser beam in infrared at 1573 nm. Investigations were directed toward verifying the limit values by defining the thresholds of corneal damage in experiments carried out on the rabbit, and using biochemi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2e12d4504a29240e0d775674d27fdea
https://doi.org/10.2351/1.2900417
https://doi.org/10.2351/1.2900417
Autor:
Dominique Dormont, Aurore Charbonnier, Jean-Philippe Deslys, Corinne Ida Lasmézas, Nicole Salès, Christian Herzog, Sophie Freire, Etchegaray N
Publikováno v:
The Lancet. 363:422-428
Summary Background The disease-associated form of prion protein (PrP res ) has been noted in lymphoreticular tissues in patients with variant Creutzfeldt-Jakob disease (vCJD). Thus, the disease could be transmitted iatrogenically by surgery or use of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f295d7b4dd0b588bff60d204725880f
https://doi.org/10.1016/s0140-6736(04)15487-1
https://doi.org/10.1016/s0140-6736(04)15487-1
Autor:
Corinne Ida Lasmézas, Dulce Papy-Garcia, Denis Barritault, Steve Simoneau, Nicole Salès, F. Lamoury, Dominique Dormont, Jean-Philippe Deslys, Karim Tarik Adjou
Publikováno v:
Journal of General Virology. 84:2595-2603
The accumulation of PrP(res), the protease-resistant abnormal form of the host-encoded cellular prion protein, PrP(C), plays a central role in transmissible spongiform encephalopathies. Human contamination by bovine spongiform encephalopathy (BSE) ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c947e9854bd2f848263696c6bab39490
https://doi.org/10.1099/vir.0.19073-0
https://doi.org/10.1099/vir.0.19073-0
Autor:
Gian Franco Sferrazza, Corinne Ida Lasmézas, Paula Saá, Sukhvir P. Mahal, Nicole Salès, Yervand E. Karapetyan, Charles Weissmann, Alexandra Sherman
Publikováno v:
PLoS ONE, Vol 4, Iss 5, p e5730 (2009)
PLoS ONE
PLoS ONE
Prion strain identification has been hitherto achieved using time-consuming incubation time determinations in one or more mouse lines and elaborate neuropathological assessment. In the present work, we make a detailed study of the properties of PrP-o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75d92b20df6402fcf14a91295a0ec0d5
http://europepmc.org/articles/PMC2684634?pdf=render
http://europepmc.org/articles/PMC2684634?pdf=render
Autor:
Marie-Magdeleine Ruchoux, Emmanuel Comoy, Frédéric Auvré, Jean-Philippe Deslys, Dominique Marcé, Sophie Freire, Nathalie Lescoutra-Etchegaray, Salvatore Monaco, Maria Caramelli, Cristina Casalone, Sergio Ferrari, Corinne Ida Lasmézas, Gianluigi Zanusso, Nicole Salès, Paul Brown, Philippe Leboulch
Publikováno v:
PLoS ONE, Vol 3, Iss 8, p e3017 (2008)
PLoS ONE
PLoS ONE
Background Human variant Creutzfeldt-Jakob Disease (vCJD) results from foodborne transmission of prions from slaughtered cattle with classical Bovine Spongiform Encephalopathy (cBSE). Atypical forms of BSE, which remain mostly asymptomatic in aging c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2f40ee99b59d17b84a2b82198bf90b6
http://europepmc.org/articles/PMC2515088?pdf=render
http://europepmc.org/articles/PMC2515088?pdf=render
Autor:
Corinne Ida Lasmézas, Elisabeth Kremmer, Pierluigi Gambetti, Jacques Grassi, Sabine Gilch, Thierry Baron, Cécile Féraudet, Nicole Salès, Chantal Mourton Gilles, Hermann M. Schätzl, Wen-Quan Zou, Maxime Lefebvre-Roque
Publikováno v:
Prion
Prion, Taylor & Francis, 2007, 1 (3), pp.198-206
Prion, 2007, 1 (3), pp.198-206
Prion, Taylor & Francis, 2007, 1 (3), pp.198-206
Prion, 2007, 1 (3), pp.198-206
The absence of specific immune response is a hallmark of prion diseases. However, in vitro and in vivo experiments have provided evidence that an anti-PrP humoral response could have beneficial effects. Prophylactic passive immunization performed at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32aac3d1074ae93f8e688fdec1ca21eb
https://europepmc.org/articles/PMC2634593/
https://europepmc.org/articles/PMC2634593/
