Zobrazeno 1 - 10
of 99
pro vyhledávání: '"Jacqueline, Mikol"'
Publikováno v:
Frontiers in Molecular Biosciences, Vol 10 (2023)
The presence of prion infectivity in the blood of patients affected by variant Creutzfeldt–Jakob disease (v-CJD), the human prion disease linked to the bovine spongiform encephalopathy (BSE), poses the risk of inter-human transmission of this fatal
Externí odkaz:
https://doaj.org/article/45a4276ce905495295d720238b02056f
Autor:
Jacqueline Mikol
Publikováno v:
Free Neuropathology, Vol 2 (2021)
Externí odkaz:
https://doaj.org/article/ac9c0a136dbf483691a127e2bbff49ed
Autor:
Emmanuel E. Comoy, Jacqueline Mikol, Nina Jaffré, Vincent Lebon, Etienne Levavasseur, Nathalie Streichenberger, Chryslain Sumian, Armand Perret-Liaudet, Marc Eloit, Olivier Andreoletti, Stéphane Haïk, Philippe Hantraye, Jean-Philippe Deslys
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-13 (2017)
It is hypothesised that exposure to bovine spongiform encephalopathy through contaminated food could have resulted in a large proportion of latent variant Creutzfeldt-Jakob disease cases in humans. Here the authors demonstrate that inoculation with b
Externí odkaz:
https://doaj.org/article/b0c9168d37d3407aa90721d13daa5b6c
Autor:
Serena Pavoni, Rafika Jarray, Ferid Nassor, Anne-Cécile Guyot, Steve Cottin, Jessica Rontard, Jacqueline Mikol, Aloïse Mabondzo, Jean-Philippe Deslys, Frank Yates
Publikováno v:
PLoS ONE, Vol 13, Iss 12, p e0209150 (2018)
Human mini-brains (MB) are cerebral organoids that recapitulate in part the complexity of the human brain in a unique three-dimensional in vitro model, yielding discrete brain regions reminiscent of the cerebral cortex. Specific proteins linked to ne
Externí odkaz:
https://doaj.org/article/42b286926f5245ecbb4e3f4752714fc2
Autor:
Paul Brown, Juan Maria Torres, Juergen A. Richt, Justin J. Greenlee, Cristina Casalone, Evelyne Correia, Capucine Dehen, Sophie Luccantoni-Freire, Valérie Durand, Marie-Madeleine Ruchoux, Jacqueline Mikol, Emmanuel E. Comoy, Jean-Philippe Deslys
Publikováno v:
Pathogens, Vol 2, Iss 3, Pp 520-532 (2013)
Successful transmission of Transmissible Mink Encephalopathy (TME) to cattle supports the bovine hypothesis for the still controversial origin of TME outbreaks. Human and primate susceptibility to classical Bovine Spongiform Encephalopathy (c-BSE) an
Externí odkaz:
https://doaj.org/article/47cd2175779f42a581a05b230271bf8d
Autor:
Jacqueline Mikol
Publikováno v:
Clinical Neuropathology. 39:152-161
After a short summary of Arnold Pick's biography, the history of how Pick's disease (PiD) was reported is presented, from its clinical symptoms to its molecular characterization. The macroscopic description of frontotemporal atrophy by Pick is recoun
Autor:
Jacqueline, Mikol
Publikováno v:
In Neuromuscular Disorders April 2011 21(4):291-297
Publikováno v:
Cell and tissue research.
The fascinating history of prion diseases is intimately linked to the use of nonhuman primates as experimental models, which brought so fundamental and founding information about transmissibility, pathogenesis, and resistance of prions. These models
Autor:
Jochen Herms, Sabina Capellari, Ignazio Cali, Bernardino Ghetti, Ellen Gelpi, Viktoria Ruf, Armin Giese, Brian S. Appleby, Marcello Rossi, Marcelo A. Barria, Pierluigi Gambetti, Jacqueline Mikol, Anna Ladogana, Diane Ritchie, Angela Mammana, Otto Windl, Piero Parchi, Suvankar Pal, Simone Baiardi
Publikováno v:
Acta Neuropathologica
Baiardi, S, Rossi, M, Mammana, A, Appleby, B S, Barria, M A, Calì, I, Gambetti, P, Gelpi, E, Giese, A, Ghetti, B, Herms, J, Ladogana, A, Mikol, J, Pal, S, Ritchie, D L, Ruf, V, Windl, O, Capellari, S & Parchi, P 2021, ' Phenotypic diversity of genetic Creutzfeldt–Jakob disease: a histo-molecular-based classification ', Acta Neuropathologica . https://doi.org/10.1007/s00401-021-02350-y
Baiardi, S, Rossi, M, Mammana, A, Appleby, B S, Barria, M A, Calì, I, Gambetti, P, Gelpi, E, Giese, A, Ghetti, B, Herms, J, Ladogana, A, Mikol, J, Pal, S, Ritchie, D L, Ruf, V, Windl, O, Capellari, S & Parchi, P 2021, ' Phenotypic diversity of genetic Creutzfeldt–Jakob disease: a histo-molecular-based classification ', Acta Neuropathologica . https://doi.org/10.1007/s00401-021-02350-y
The current classification of sporadic Creutzfeldt–Jakob disease (sCJD) includes six major clinicopathological subtypes defined by the physicochemical properties of the protease-resistant core of the pathologic prion protein (PrPSc), defining two m
Autor:
Danielle Seilhean, Jacqueline Mikol
Publikováno v:
Clinical Neuropathology. 37:193-196