J. Deslys

发表

Distribution and submicroscopic immunogold localization of cellular prion protein (PrPc) in extracerebral tissues

D. Dormont, P. Brown, T. Billette de Villemeur, 1998, Cell and Tissue Research.

Perthame. Conservative cross diffusions and pattern formation through

B. Perthame, D. Oelz, A. Stevens, 2010 .

Experimental transfusion of variant CJD-infected blood reveals previously uncharacterised prion disorder in mice and macaque

O. Andréoletti, P. Hantraye, V. Lebon, 2017, Nature Communications.

Time-course studies of 14-3-3 protein isoforms in cerebrospinal fluid and brain of primates after oral or intracerebral infection with bovine spongiform encephalopathy agent.

J. Löwer, U. Hahmann, J. Deslys, 2007, The Journal of general virology.

PEGylated polycyanoacrylate nanoparticles as vector for drug delivery in prion diseases

P. Couvreur, D. Dormont, I. Brigger, 2001, Journal of Neuroscience Methods.

Ultrastructural localization of cellular prion protein (PrPc) at the neuromuscular junction

J. Fournier, F. Escaig-Haye, C. Lasmézas, 1999, Journal of neuroscience research.

Immune system-dependent and -independent replication of the scrapie agent

C. Locht, J. Cesbron, D. Dormont, 1996, Journal of virology.

Atypical BSE (BASE) Transmitted from Asymptomatic Aging Cattle to a Primate

P. Brown, P. Leboulch, G. Zanusso, 2008, PloS one.

Creutzfeldt-Jakob disease with unusually extensive neuropathology in a child treated with native human growth hormone

H. Budka, P. Brown, J. Mikol, 2012, Clinical neuropathology.

Risk of oral infection with bovine spongiform encephalopathy agent in primates

F. Mouthon, T. Konold, P. Brown, 2005, The Lancet.

Creutzfeldt-Jakob disease from contaminated growth hormone extracts in France

Y. Agid, M. Ruberg, J. Hauw, 1996, Neurology.

This is really a case of new variant Creutzfeldt-Jakob

G. Chazot, J. Deslys, N. Kopp, 2001, Acta Neuropathologica.

Diagnosis of bovine spongiform encephalopathy.

J. Deslys, E. Comoy, C. Lasmézas, 2001, Veterinary journal.

Neuropathologic variants of sporadic Creutzfeldt–Jakob disease and codon 129 of PrP gene

J. Hauw, D. Dormont, J. Laplanche, 2000, Neurology.

Incubation period of Creutzfeldt–Jakob disease in human growth hormone recipients in France

Y. Agid, J. Hauw, A. Alpérovitch, 1999, Neurology.

Prospects for the Pharmacological Treatment of Human Prion Diseases

D. Dormont, M. Seman, K. Adjou, 1998 .

Creutzfeldt-Jakob disease: therapeutic strategies.

D. Dormont, V. Béringue, K. Adjou, 1997, Expert opinion on investigational drugs.

Strain specific and common pathogenic events in murine models of scrapie and bovine spongiform encephalopathy.

J. Hauw, D. Dormont, K. Adjou, 1996, The Journal of general virology.

A simple and rapid method for sequencing the entire coding region of the human prion protein (PrP) gene

D. Dormont, J. Deslys, A. Jaegly, 1994, Journal of Neuroscience Methods.

Selection of specific strains in iatrogenic Creutzfeldt-Jakob disease

D. Dormont, J. Deslys, C. Lasmézas, 1994, The Lancet.

Prion strains associated with iatrogenic CJD in French and UK human growth hormone recipients

P. Péran, O. Andréoletti, S. Lugan, 2021, Acta Neuropathologica Communications.

D. Dormont, J. Deslys, D. Marcé, 1994, The Journal of general virology.

Creutzfeldt‐Jakob disease after pituitary‐derived human growth hormone therapy

D. Leys, C. Fallet-Bianco, D. Dormont, 1994, Neurology.

Edinburgh Research Explorer Differential overexpression of SERPINA3 in human prion diseases

I. Ferrer, F. Tagliavini, G. Legname, 2022 .

Transmission of scrapie prions to primate after an extended silent incubation period

J. Richt, P. Brown, O. Andréoletti, 2015, Scientific Reports.

BSE agent signatures in a goat

P. Sarradin, O. Andréoletti, S. Simon, 2005, Veterinary Record.

Alpha-synuclein accumulates in the brain of scrapie-affected sheep and goats.

K. El-Hachimi, K. Adjou, J. Deslys, 2007, Journal of comparative pathology.

Creutzfeldt-Jakob disease

D. Dormont, J. Deslys, T. D. Villemeur, 1996, The Lancet.

PrPTSE Distribution in a Primate Model of Variant, Sporadic, and Iatrogenic Creutzfeldt-Jakob Disease

C. Herzog, J. Deslys, N. Salès, 2005, Journal of Virology.

Unexpected prion phenotypes in experimentally transfused animals: predictive models for humans?

J. Mikol, J. Deslys, E. Comoy, 2018, Prion.

Non-human primates in prion diseases

J. Mikol, J. Deslys, E. Comoy, 2022, Cell and Tissue Research.

Preclinical Detection of Variant CJD and BSE Prions in Blood

M. Moudjou, O. Andréoletti, C. Lacroux, 2014, PLoS pathogens.

Removal of exogenous prion infectivity in leukoreduced red blood cells unit by a specific filter designed for human transfusion

J. Deslys, P. V. Gurgel, E. Comoy, 2014, Transfusion.

Blood reference materials from macaques infected with variant Creutzfeldt‐Jakob disease agent

Nabanita Nag, D. Asher, Kristen L. McDowell, 2015, Transfusion.

Evaluation of the Zoonotic Potential of Transmissible Mink Encephalopathy

J. Richt, P. Brown, J. Torres, 2013, Pathogens.

Role of gut macrophages in mice orally contaminated with scrapie or BSE.

P. Couvreur, E. Fattal, J. Deslys, 2005, International journal of pharmaceutics.

Sensitive detection of aggregated prion protein via proximity ligation

U. Landegren, T. Linné, M. Kamali-Moghaddam, 2014, Prion.

Increase of monoamine oxidase-B activity in the brain of scrapie-infected hamsters

D. Dormont, M. Seman, K. Adjou, 2008, Neurochemistry International.

Pathogenesis of the oral route of infection of mice with scrapie and bovine spongiform encephalopathy agents.

D. Dormont, V. Béringue, J. Deslys, 1999, The Journal of general virology.

Polyene Antibiotics in Experimental Transmissible Subacute Spongiform Encephalopathies

D. Dormont, M. Seman, V. Béringue, 1998 .

Probing the dynamics of prion diseases with amphotericin B.

D. Dormont, K. Adjou, J. Deslys, 1997, Trends in microbiology.

Modulation of prion protein gene expression by growth factors in cultured mouse astrocytes and PC-12 cells.

D. Dormont, J. Deslys, P. Castelnau, 1994, Brain research. Molecular brain research.

Regulation of the glial fibrillary acidic protein, beta actin and prion protein mRNAs during brain development in mouse.

D. Dormont, J. Deslys, F. Lazarini, 1991, Brain research. Molecular brain research.

Evaluation of the protection of primates transfused with variant Creutzfeldt‐Jakob disease–infected blood products filtered with prion removal devices: a 5‐year update

J. Mikol, J. Deslys, E. Comoy, 2015, Transfusion.

Long Term Gene Expression in Human Induced Pluripotent Stem Cells and Cerebral Organoids to Model a Neurodegenerative Disease

D. Biard, D. Papy-Garcia, J. Deslys, 2020, Frontiers in Cellular Neuroscience.

Small critical RNAs in the scrapie agent

P. Lebon, M. Ruchoux, N. Vignier, 2009 .

Synthetic Scrapie Infectivity: Interaction between Recombinant PrP and Scrapie Brain-Derived RNA

M. Beekes, A. Thomzig, P. Lebon, 2015, Virulence.

Prion Protein is Not Detectable in Dental Pulp from Patients with Creutzfeldt-Jakob Disease

J. Hauw, J. Cesbron, D. Dormont, 2000, Journal of dental research.

Prion Protein Gene Expression in Cultured Astrocytes Treated by Recombinant Growth Hormone and Insulin-like Growth Factor

D. Dormont, J. Deslys, P. Castelnau, 1994, Experimental Neurology.

Gene Expression in Scrapie CLONING OF A NEW SCRAPIE-RESPONSIVE GENE AND THE IDENTIFICATION OF INCREASED LEVELS OF SEVEN OTHER mRNA TRANSCRIPTS*

D. Dormont, M. Dron, J. Deslys, 1998 .

Different Isoforms of the Non-Integrin Laminin Receptor Are Present in Mouse Brain and Bind PrP

D. Dormont, S. Haïk, J. Deslys, 2003, Biological chemistry.

Neurotoxicity of the Putative Transmembrane Domain of the Prion Protein

R. Brasseur, L. Lins, F. Tagliavini, 2000, Neurobiology of Disease.

Effects of the polyene antibiotic derivative MS-8209 on the astrocyte lysosomal system of scrapie-infected hamsters

D. Dormont, M. Seman, K. Adjou, 2002, Journal of Molecular Neuroscience.

Process for purifying PrPres from a biological sample and its applications

J. Deslys, 1998 .

Late treatment with polyene antibiotics can prolong the survival time of scrapie-infected animals

D. Dormont, M. Seman, V. Béringue, 1997, Journal of virology.

Role of spleen macrophages in the clearance of scrapie agent early in pathogenesis

Patrick Couvreur, Vincent Beringue, P. Couvreur, 2000, The Journal of pathology.

Iatrogenic Creutzfeldt-Jakob disease in three growth hormone recipients: a neuropathological study.

C. Duyckaerts, D. Dormont, A. Gelot, 1994, Neuropathology and applied neurobiology.

Prion inactivation using a new gaseous hydrogen peroxide sterilisation process.

G. Mcdonnell, G. Fichet, J. Deslys, 2007, The Journal of hospital infection.

Investigations of a prion infectivity assay to evaluate methods of decontamination.

G. Mcdonnell, G. Fichet, J. Deslys, 2007, Journal of microbiological methods.

Novel methods for disinfection of prion-contaminated medical devices

P. Brown, G. Mcdonnell, G. Fichet, 2004, The Lancet.

Inactivation of Bacteria and Biomolecules by Low-Pressure Plasma Discharges

A. Yanguas-Gil, F. Rossi, P. Awakowicz, 2010 .

Nervous and nonnervous cell transduction by recombinant adenoviruses that inducibly express the human PrP.

D. Dormont, F. Mouthon, B. Klonjkowski, 2001, Biochemical and biophysical research communications.

The 37‐kDa/67‐kDa laminin receptor acts as the cell‐surface receptor for the cellular prion protein

D. Dormont, S. Haïk, J. Peyrin, 2001, The EMBO journal.

Identification of interaction domains of the prion protein with its 37‐kDa/67‐kDa laminin receptor

D. Dormont, S. Haïk, J. Peyrin, 2001, The EMBO journal.

Hemoglobin mRNA Changes in the Frontal Cortex of Patients with Neurodegenerative Diseases

F. Tagliavini, G. Legname, I. Ferrer, 2018, Front. Neurosci..

Differential overexpression of SERPINA3 in human prion diseases

I. Ferrer, F. Tagliavini, G. Legname, 2017, Scientific Reports.

Transmission of the BSE Agent to Mice in the Absence of Detectable Abnormal Prion Protein

J. Rossier, J. Hauw, D. Dormont, 1997, Science.

Transgenic mouse models expressing human and macaque prion protein exhibit similar prion susceptibility on a strain-dependent manner

J. Torres, M. Birling, J. Deslys, 2019, Scientific Reports.

Sensitive Detection of Prion Proteins by Immunoassay: CEA/Bio-Rad Test

J. Grassi, J. Deslys, E. Comoy, 2003 .

New use of a material capable of binding the prion protein

J. Deslys, E. Comoy, N. Jaffré, 2011 .

[Creutzfeldt-Jakob disease in 4 children treated with growth hormone].

D. Dormont, T. Billette de Villemeur, P. Beauvais, 1992, Revue neurologique.

Astrocyte gene expression in experimental mouse scrapie.

D. Dormont, M. Tardy, J. Deslys, 1994, Journal of comparative pathology.

Small-molecule induction of Aβ-42 peptide production in human cerebral organoids to model Alzheimer's disease associated phenotypes

J. Mikol, J. Deslys, F. Yates, 2018, PloS one.

Direct neural transmission of vCJD/BSE in macaque after finger incision

J. Mikol, J. Deslys, E. Comoy, 2020, Acta Neuropathologica.

Dual Conformation of H2H3 Domain of Prion Protein in Mammalian Cells

H. Rezaei, J. Deslys, S. Prigent, 2011, The Journal of Biological Chemistry.

New insight into abnormal prion protein using monoclonal antibodies.

D. Dormont, J. Grassi, C. Créminon, 1999, Biochemical and biophysical research communications.

Search for a Nuclear Localization Signal in the Prion Protein

D. Dormont, F. Mouthon, J. Peyrin, 1998, Molecular and Cellular Neuroscience.

Comparative Molecular Analysis of the Abnormal Prion Protein in Field Scrapie Cases and Experimental Bovine Spongiform Encephalopathy in Sheep by Use of Western Blotting and Immunohistochemical Methods

S. Simon, J. Grassi, S. Lezmi, 2004, Journal of Virology.

Gene Expression in Scrapie

D. Dormont, M. Dron, J. Deslys, 1998, The Journal of Biological Chemistry.

BSE transmission to macaques

J. Hauw, D. Dormont, J. Ironside, 1996, Nature.

Size distribution dependence of prion aggregates infectivity.

Dietmar Oelz, Benoît Perthame, Vincent Calvez, 2009, Mathematical biosciences.

Bimodality, prion aggregates infectivity and prediction of strain phenomenon

B. Perthame, D. Oelz, V. Calvez, 2008, 0802.2024.

Prion dynamics with size dependency–strain phenomena

V. Calvez, F. Mouthon, M. Doumic, 2010, Journal of biological dynamics.

Glycosylation-related Gene Expression in Prion Diseases

L. Forestier, J. Deslys, R. Julien, 2005, Journal of Biological Chemistry.

New inhibitors of prion replication that target the amyloid precursor.

E. Jacquet, F. Mouthon, M. Charvériat, 2009, The Journal of general virology.

Variations in prion protein and glial fibrillary acidic protein mRNAs in the brain of scrapie-infected newborn mouse.

D. Dormont, J. Deslys, F. Lazarini, 1992, The Journal of general virology.

Decontamination of prions in a plasma product manufacturing environment

H. Laude, J. Deslys, A. Bellon, 2014, Transfusion.

Prion infection-impaired functional blocks identified by proteomics enlighten the targets and the curing pathways of an anti-prion drug.

J. Grosclaude, V. Labas, F. Mouthon, 2007, Biochimica et biophysica acta.

Proof-of-Concept Study of Drug Brain Permeability Between in Vivo Human Brain and an in Vitro iPSCs-Human Blood-Brain Barrier Model

O. Langer, A. Pruvost, N. Costa, 2019, Scientific Reports.

Adaptation of the bovine spongiform encephalopathy agent to primates and comparison with Creutzfeldt– Jakob disease: Implications for human health

J. Hauw, D. Dormont, J. Ironside, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Genotype at codon 129 and susceptibility to Creutzfeldt-Jakob disease

D. Dormont, F. Mouthon, J. Deslys, 1998, The Lancet.

Cold Atmospheric Plasma for the Decontamination of Reusable Surgical Instruments

M. Kong, J. Deslys, E. Comoy, 2010 .

Pharmacological studies of a new derivative of amphotericin B, MS-8209, in mouse and hamster scrapie.

D. Dormont, M. Seman, K. Adjou, 1994, The Journal of general virology.

Encephalopathy induced by Alzheimer brain inoculation in a non-human primate

L. Buée, F. Petit, C. Duyckaerts, 2019, Acta Neuropathologica Communications.

A novel generation of heparan sulfate mimetics for the treatment of prion diseases.

D. Dormont, D. Papy-Garcia, K. Adjou, 2003, The Journal of general virology.

Structure-activity studies of heparan mimetic polyanions for anti-prion therapies.

G. Carpentier, D. Papy-Garcia, K. Adjou, 2007, Biochemical and biophysical research communications.

Evaluation of Quinacrine Treatment for Prion Diseases

G. Forloni, F. Tagliavini, M. Salmona, 2003, Journal of Virology.

Microglial cells respond to amyloidogenic PrP peptide by the production of inflammatory cytokines.

F. Tagliavini, D. Dormont, M. Salmona, 1999, Neuroreport.

Comparison of CR36, a new heparan mimetic, and pentosan polysulfate in the treatment of prion diseases.

P. Brown, D. Papy-Garcia, D. Barritault, 2007, The Journal of general virology.

Unexpected decrease of full-length prion protein in macaques inoculated with prion-contaminated blood products

J. Mikol, J. Deslys, E. Comoy, 2023, Frontiers in Molecular Biosciences.

Iatrogenic transmission of Alzheimer's disease: Evidence based on experimental inoculation of Alzheimer's brains into a primate

F. Petit, C. Duyckaerts, S. Sawiak, 2020 .

Cleaning, disinfection and sterilization of surface prion contamination.

V. Thomas, G. Mcdonnell, J. Deslys, 2013, The Journal of hospital infection.

Opposite Effects of Dextran Sulfate 500, the Polyene Antibiotic MS-8209, and Congo Red on Accumulation of the Protease-Resistant Isoform of PrP in the Spleens of Mice Inoculated Intraperitoneally with the Scrapie Agent

D. Dormont, V. Béringue, K. Adjou, 2000, Journal of Virology.

The prion protein is critical for DNA repair and cell survival after genotoxic stress

G. Tell, J. Radicella, A. Bravard, 2014, Nucleic acids research.

Specific determination of the proteinase K-resistant form of the prion protein using two-site immunometric assays. Application to the post-mortem diagnosis of BSE.

J. Grassi, C. Créminon, Y. Frobert, 2000, Archives of virology. Supplementum.

Screening slaughtered cattle for BSE.

S. Simon, J. Grassi, H. Schimmel, 2001, Nature.

Edinburgh Research Explorer Differential overexpression of SERPINA3 in human prion diseases

I. Ferrer, F. Tagliavini, G. Legname, 2022 .

Tissue distribution of bovine spongiform encephalopathy agent in primates after intravenous or oral infection

D. Dormont, C. Herzog, J. Deslys, 2004, The Lancet.

Methode de criblage de substances a action therapeutique dans le traitement des encephalopathies subaigues spongiformes transmissibles

V. Béringue, J. Deslys, C. Lasmézas, 1998 .

MS-8209, an amphotericin B analogue, delays the appearance of spongiosis, astrogliosis and PrPres accumulation in the brain of scrapie-infected hamsters.

J. Hauw, D. Dormont, M. Seman, 2000, Journal of comparative pathology.

Mechanistic insights into cellular alteration of prion by poly‐D‐lysine: the role of H2H3 domain

A. Pastore, F. Mouthon, H. Rezaei, 2011, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Dementia with Lewy bodies in a neuropathologic series of suspected Creutzfeldt–Jakob disease

C. Duyckaerts, J. Laplanche, A. Laquérriere, 2000, Neurology.

MS-8209, a new amphotericin B derivative, provides enhanced efficacy in delaying hamster scrapie

D. Dormont, M. Seman, K. Adjou, 1995, Antimicrobial agents and chemotherapy.

Differential effects of a new amphotericin B derivative, MS-8209, on mouse BSE and scrapie: implications for the mechanism of action of polyene antibiotics.

D. Dormont, M. Seman, K. Adjou, 1996, Research in virology.

Inhibiting scrapie neuroinvasion by polyene antibiotic treatment of SCID mice.

K. Adjou, J. Deslys, R. Demaimay, 1999, The Journal of general virology.

Ultrastructural evidence that ependymal cells are infected in experimental scrapie

K. Adjou, J. Fournier, J. Deslys, 2008, Acta Neuropathologica.

Diagnostic Method of esst caused by a strain of NCTA in a biological sample and its use in the differential diagnosis of various UTA strains

J. Grassi, J. Deslys, E. Comoy, 1999 .

Three-dimensional molecular cartography of human cerebral organoids revealed by double-barcoded spatial transcriptomics

M. Mendoza-Parra, J. Deslys, Julien Moehlin, 2023, Cell reports methods.

A 3-dimensional molecular cartography of human cerebral organoids revealed by double-barcoded spatial transcriptomics

M. Mendoza-Parra, J. Deslys, Julien Moehlin, 2023, bioRxiv.

MRI and the second French case of vCJD

Bertrand Fontaine, Catherine Oppenheim, J. Hauw, 2000, The Lancet.