Výsledky vyhledávání - "Daisy Bougard"

Akademický článek

Protease-Sensitive and -Resistant Forms of Human and Murine Alpha-Synucleins in Distinct Brain Regions of Transgenic Mice (M83) Expressing the Human Mutated A53T Protein

Autor: Dominique Bétemps, Jean-Noël Arsac, Simon Nicot, Dominique Canal, Habiba Tlili, Maxime Belondrade, Eric Morignat, Jérémy Verchère, Damien Gaillard, Lilian Bruyère-Ostells, Charly Mayran, Latifa Lakhdar, Daisy Bougard, Thierry Baron

Publikováno v: Biomolecules, Vol 13, Iss 12, p 1788 (2023)

Human neurodegenerative diseases associated with the misfolding of the alpha-synuclein (aS) protein (synucleinopathies) are similar to prion diseases to the extent that lesions are spread by similar molecular mechanisms. In a transgenic mouse model (

Externí odkaz: https://doaj.org/article/1128120990944ed0a7c02b0c20ba60b1

Zobrazit plný text záznamu

Akademický článek

Sensitive protein misfolding cyclic amplification of sporadic Creutzfeldt–Jakob disease prions is strongly seed and substrate dependent

Autor: Maxime Bélondrade, Simon Nicot, Charly Mayran, Lilian Bruyere-Ostells, Florian Almela, Michele A. Di Bari, Etienne Levavasseur, Joel C. Watts, Chantal Fournier-Wirth, Sylvain Lehmann, Stéphane Haïk, Romolo Nonno, Daisy Bougard

Publikováno v: Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)

Abstract Unlike variant Creutzfeldt–Jakob disease prions, sporadic Creutzfeldt–Jakob disease prions have been shown to be difficult to amplify in vitro by protein misfolding cyclic amplification (PMCA). We assessed PMCA of pathological prion prot

Externí odkaz: https://doaj.org/article/49816cda18ac44b7b8c29880c7045392

Zobrazit plný text záznamu

Plný text ve formátu HTML

Akademický článek

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

Autor: Maxime Bélondrade, Christelle Jas-Duval, Simon Nicot, Lilian Bruyère-Ostells, Charly Mayran, Laetitia Herzog, Fabienne Reine, Juan Maria Torres, Chantal Fournier-Wirth, Vincent Béringue, Sylvain Lehmann, Daisy Bougard

Publikováno v: mSphere, Vol 5, Iss 1 (2020)

ABSTRACT To date, approximately 500 iatrogenic Creutzfeldt-Jakob disease cases have been reported worldwide, most of them resulting from cadaveric dura mater graft and from the administration of prion-contaminated human growth hormone. The unusual re

Externí odkaz: https://doaj.org/article/3d2a5e8a73704172bed30f81758f857a

Zobrazit plný text záznamu

Akademický článek

Diagnosis of Methionine/Valine Variant Creutzfeldt-Jakob Disease by Protein Misfolding Cyclic Amplification

Autor: Daisy Bougard, Maxime Bélondrade, Charly Mayran, Lilian Bruyère-Ostells, Sylvain Lehmann, Chantal Fournier-Wirth, Richard S. Knight, Robert G. Will, Alison J.E. Green

Publikováno v: Emerging Infectious Diseases, Vol 24, Iss 7, Pp 1364-1366 (2018)

A patient with a heterozygous variant of Creutzfeldt-Jakob disease (CJD) with a methionine/valine genotype at codon 129 of the prion protein gene was recently reported. Using an ultrasensitive and specific protein misfolding cyclic amplification–ba

Externí odkaz: https://doaj.org/article/8150508ff793474da938b30f687519fe

Zobrazit plný text záznamu

Akademický článek

Rapid and Highly Sensitive Detection of Variant Creutzfeldt-Jakob Disease Abnormal Prion Protein on Steel Surfaces by Protein Misfolding Cyclic Amplification: Application to Prion Decontamination Studies.

Autor: Maxime Belondrade, Simon Nicot, Vincent Béringue, Joliette Coste, Sylvain Lehmann, Daisy Bougard

Publikováno v: PLoS ONE, Vol 11, Iss 1, p e0146833 (2016)

The prevalence of variant Creutzfeldt-Jakob disease (vCJD) in the population remains uncertain, although it has been estimated that 1 in 2000 people in the United Kingdom are positive for abnormal prion protein (PrPTSE) by a recent survey of archived

Externí odkaz: https://doaj.org/article/00e8746623ad4a229458cb98aeb96b48

Zobrazit plný text záznamu

Akademický článek

Plasminogen-based capture combined with amplification technology for the detection of PrP(TSE) in the pre-clinical phase of infection.

Autor: Christiane Segarra, Daisy Bougard, Mohammed Moudjou, Hubert Laude, Vincent Béringue, Joliette Coste

Publikováno v: PLoS ONE, Vol 8, Iss 7, p e69632 (2013)

BackgroundVariant Creutzfeldt-Jakob disease (vCJD) is a neurodegenerative infectious disorder, characterized by a prominent accumulation of pathological isoforms of the prion protein (PrP(TSE)) in the brain and lymphoid tissues. Since the publication

Externí odkaz: https://doaj.org/article/32c156f7feb248f1a9805fb7b607648e

Zobrazit plný text záznamu

Akademický článek

Impact of leucocyte depletion and prion reduction filters on TSE blood borne transmission.

Autor: Caroline Lacroux, Daisy Bougard, Claire Litaise, Hugh Simmons, Fabien Corbiere, Dominique Dernis, René Tardivel, Nathalie Morel, Stephanie Simon, Séverine Lugan, Pierrette Costes, Jean Louis Weisbecker, François Schelcher, Jacques Grassi, Joliette Coste, Olivier Andréoletti

Publikováno v: PLoS ONE, Vol 7, Iss 7, p e42019 (2012)

The identification in the UK of 4 v-CJD infected patients thought to be due to the use of transfused Red Blood Cell units prepared from blood of donors incubating v-CJD raised major concerns in transfusion medicine. The demonstration of leucocyte ass

Externí odkaz: https://doaj.org/article/91a99f92206748e18af2781e66be0343

Zobrazit plný text záznamu

Detection of Amyloid-β Fibrils Using Track-Etched Nanopores: Effect of Geometry and Crowding

Autor: Nicolas Arroyo, Jean-Marc Janot, Anna Stevenson, Imad Abrao Nemeir, Véronique Perrier, Jérémy Bentin, Daisy Bougard, Didier Cot, Mathilde Lepoitevin, Nathan Meyer, Joan Torrent, Sebastien Balme, Fabien Picaud, Maxime Belondrade

Publikováno v: ACS Sensors. 6:3733-3743

Several neurodegenerative diseases have been linked to proteins or peptides that are prone to aggregate in different brain regions. Aggregation of amyloid-β (Aβ) peptides is recognized as the main cause of Alzheimer's disease (AD) progression, lead

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6a8a6c9c7f8a6598785ef9abc93e14c
https://doi.org/10.1021/acssensors.1c01523

Zobrazit plný text záznamu

Variant Creutzfeldt–Jakob Disease Diagnosed 7.5 Years after Occupational Exposure

Autor: Isabelle Plu, Audrey Culeux, Elodie Bouaziz-Amar, Danielle Seilhean, Stéphane Haïk, M Bustuchina Vlaicu, Maxime Belondrade, Katarina Grznarova, Jean-Philippe Brandel, Daisy Bougard, Michèle Levasseur, Angeline Denouel

Publikováno v: New England Journal of Medicine
New England Journal of Medicine, 2020, 383 (1), pp.83-85. ⟨10.1056/NEJMc2000687⟩

Variant CJD in a Laboratory Technician Variant Creutzfeldt–Jakob disease was identified in a technician who had cut her thumb while handling brain sections of mice infected with adapted BSE 7.5 yea...

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45ea9d89b0f77fcb5ca39f4cea4f4596
https://doi.org/10.1056/nejmc2000687

Zobrazit plný text záznamu

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

Autor: Daisy Bougard, Vincent Béringue, Lilian Bruyère-Ostells, Maxime Belondrade, Laetitia Herzog, Fabienne Reine, Chantal Fournier-Wirth, Juan María Torres, Christelle Jas-Duval, Sylvain Lehmann, Charly Mayran, Simon Nicot

Publikováno v: MSphere
MSphere, American Society for Microbiology., 2020, 5 (1), ⟨10.1128/mSphere.00649-19⟩
mSphere
mSphere, Vol 5, Iss 1 (2020)
mSphere, Vol 5, Iss 1, p e00649-19 (2020)

Creutzfeldt-Jakob diseases are neurodegenerative disorders for which transmission linked to medical procedures have been reported in hundreds of patients. As prion diseases, they are characterized by an unusual resistance to conventional decontaminat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c19a52b38f606ac0bd5407d78024a918
https://hal.umontpellier.fr/hal-03116427

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání