S. Lehmann

发表

Cyclodextrins Inhibit Replication of Scrapie Prion Protein in Cell Culture

M. Sy, Marguerite Prior, S. Lehmann, 2007, Journal of Virology.

Phorbol Ester-regulated Cleavage of Normal Prion Protein in HEK293 Human Cells and Murine Neurons*

F. Checler, B. Vincent, E. Paitel, 2000, The Journal of Biological Chemistry.

An innovative biologic recycling process of leukoreduction filters to produce active human antimicrobial peptides

S. Lehmann, K. Brodolin, C. Fournier-Wirth, 2014, Transfusion.

Mutant and Infectious Prion Proteins Display Common Biochemical Properties in Cultured Cells (*)

D. Harris, S. Lehmann, 1996, The Journal of Biological Chemistry.

Efficient inhibition of infectious prions multiplication and release by targeting the exosomal pathway

L. Schaeffer, G. Raposo, P. Leblanc, 2015, Cellular and Molecular Life Sciences.

A Mutant Prion Protein Displays an Aberrant Membrane Association When Expressed in Cultured Cells (*)

D. Harris, S. Lehmann, 1995, The Journal of Biological Chemistry.

Stimulation of PrPC Retrograde Transport toward the Endoplasmic Reticulum Increases Accumulation of PrPSc in Prion-infected Cells*

B. Goud, A. Mangé, S. Lehmann, 2002, The Journal of Biological Chemistry.

BSE infection of the small short-lived primate Microcebus murinus.

A. Delacourte, D. Dormont, P. Brown, 2002, Comptes rendus biologies.

Familial Prion Diseases Modeled in Cell Culture

D. Harris, S. Lehmann, N. Daude, 1998 .

A wild-type prion protein does not acquire properties of the scrapie isoform when coexpressed with a mutant prion protein in cultured cells.

D. Harris, S. Lehmann, N. Daude, 1997, Brain research. Molecular brain research.

Prion‐like protein Doppel expression is not modified in scrapie‐infected cells and in the brains of patients with Creutzfeldt–Jakob disease

J. Laplanche, P. Beaudry, S. Lehmann, 2003, FEBS letters.

[The prion protein].

S. Lehmann, 2002, Journal de la Societe de biologie.

Wild-Type Mouse Prion Protein Neuroblastoma Cell Lines Overexpressing Mouse-Adapted Scrapie Strains to Murine Successful Transmission of Three

D. Harris, H. Laude, J. Grassi, 1999 .

A novel copper-hydrogen peroxide formulation for prion decontamination.

J. Solassol, S. Lehmann, M. Pastore, 2006, The Journal of infectious diseases.

Metal ions and prion diseases.

S. Lehmann, 2002, Current opinion in chemical biology.

Neuropathology of iatrogenic Creutzfeldt–Jakob disease and immunoassay of French cadaver-sourced growth hormone batches suggest possible transmission of tauopathy and long incubation periods for the transmission of Abeta pathology

C. Duyckaerts, S. Lehmann, K. Ando, 2018, Acta Neuropathologica.

Prion protein as trans-interacting partner for neurons is involved in neurite outgrowth and neuronal survival

M. Schachner, A. Mangé, S. Lehmann, 2003, Molecular and Cellular Neuroscience.

From stem cells to prion signalling.

M. Ermonval, S. Lehmann, S. Mouillet-Richard, 2002, Comptes rendus biologies.

PrP Expression and Replication by Schwann Cells: Implications in Prion Spreading

J. Cesbron, J. Chauvin, J. Grassi, 2002, Journal of Virology.

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

V. Béringue, J. Torres, S. Lehmann, 2020, mSphere.

Systemic Delivery of siRNA Down Regulates Brain Prion Protein and Ameliorates Neuropathology in Prion Disorder

A. Gabelle, S. Lehmann, S. Resina, 2014, PloS one.

Transmissible Spongiform Encephalopathies or Prion Diseases - General Introduction

J. Grassi, S. Lehmann, 2004 .

Prion Infection Impairs Copper Binding of Cultured Cells*

A. Favier, A. Mangé, W. Rachidi, 2003, The Journal of Biological Chemistry.

PrP‐dependent cell adhesion in N2a neuroblastoma cells

A. Mangé, D. Harris, S. Lehmann, 2002, FEBS letters.

Brain and buffy coat transmission of bovine spongiform encephalopathy to the primate Microcebus murinus

D. Dormont, P. Brown, S. Lehmann, 2002, Transfusion.

Epidemiological and experimental studies on a new incident of transmissible mink encephalopathy.

S. Lehmann, R. Marsh, R. Bessen, 1991, The Journal of general virology.

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

A. Green, S. Lehmann, C. Fournier-Wirth, 2018, Emerging infectious diseases.

New hospital disinfection processes for both conventional and prion infectious agents compatible with thermosensitive medical equipment.

S. Lehmann, M. Pastore, G. Rauwel, 2009, The Journal of hospital infection.

Alpha‐ and beta‐ cleavages of the amino‐terminus of the cellular prion protein

T. Onodera, A. Mangé, S. Lehmann, 2004, Biology of the cell.

Role of an Endogenous Mannosyl-Lectin in Myelination and Stabilization of Myelin Structure

S. Lehmann, G. Vincendon, J. Zanetta, 1990 .

Prion infection impairs the cellular response to oxidative stress.

A. Favier, A. Mangé, W. Rachidi, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Cleavage of the Amino Terminus of the Prion Protein by Reactive Oxygen Species*

A. Mangé, S. Lehmann, H. E. McMahon, 2001, The Journal of Biological Chemistry.

The scrapie prion protein is present in flotillin‐1‐positive vesicles in central‐ but not peripheral‐derived neuronal cell lines

S. Lehmann, I. Maridonneau-Parini, F. Pimpinelli, 2005, The European journal of neuroscience.

Lesion-induced re-expression of neonatal recognition molecules in adult rat cerebellum

S. Lehmann, G. Vincendon, J. Zanetta, 1993, Brain Research Bulletin.

Endogenous Lectin Cerebellar Soluble Lectin Involved in Myelination Is Absent from Nonmyelinating Schwann Cells

S. Lehmann, G. Vincendon, S. Kuchler, 1992, Journal of neurochemistry.

Prion protein protects against DNA damage induced by paraquat in cultured cells.

A. Favier, W. Rachidi, S. Lehmann, 2004, Free radical biology & medicine.

Trehalose impairs aggregation of PrPSc molecules and protects prion-infected cells against oxidative damage.

S. Lehmann, C. Crozet, A. Goldsborough, 2008, Biochemical and biophysical research communications.

Prion protein suppresses perturbation of cellular copper homeostasis under oxidative conditions.

S. Itohara, A. Sakudo, E. Yoshimura, 2004, Biochemical and biophysical research communications.

Prions Impair Bioaminergic Functions through Serotonin- or Catecholamine-derived Neurotoxins in Neuronal Cells*

J. Launay, H. Laude, J. Grassi, 2008, Journal of Biological Chemistry.

[Cellular and scrapie prion proteins: which is the more toxic isoform?].

S. Lehmann, O. Milhavet, 2004, Medecine sciences : M/S.

Identification of Intermediate Steps in the Conversion of a Mutant Prion Protein to a Scrapie-like Form in Cultured Cells*

D. Harris, S. Lehmann, N. Daude, 1997, The Journal of Biological Chemistry.

Amphotericin B Inhibits the Generation of the Scrapie Isoform of the Prion Protein in Infected Cultures

A. Mangé, S. Lehmann, H. E. McMahon, 2000, Journal of Virology.

Glycoproteins and lectins in cell adhesion and cell recognition processes

S. Lehmann, P. Dufourcq, G. Vincendon, 1992, The Histochemical Journal.

Sulfated Glycans Stimulate Endocytosis of the Cellular Isoform of the Prion Protein, PrPC, in Cultured Cells (*)

K. Moulder, D. Harris, S. Shyng, 1995, The Journal of Biological Chemistry.

Trafficking of the cellular isoform of the prion protein.

A. Mangé, S. Lehmann, O. Milhavet, 1999, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

An endogenous lectin and its glycoprotein ligands are triggering basal and axon-induced Schwann cell proliferation.

S. Lehmann, S. Kuchler-Bopp, A. Badache, 1995, Glycobiology.

Mouse neuroblastoma cells release prion infectivity associated with exosomal vesicles

G. Raposo, J. Darlix, P. Leblanc, 2008, Biology of the cell.

Evidence for a Six-transmembrane Domain Structure of Presenilin 1*

D. Harris, R. Chiesa, S. Lehmann, 1997, The Journal of Biological Chemistry.

Stem cell therapy extends incubation and survival time in prion-infected mice in a time window-dependant manner.

J. Torres, S. Lehmann, C. Crozet, 2011, The Journal of infectious diseases.

The Human “Prion-like” Protein Doppel Is Expressed in Both Sertoli Cells and Spermatozoa*

J. Laplanche, J. Launay, J. Grassi, 2002, The Journal of Biological Chemistry.

Scrapie-like prion protein is translocated to the nuclei of infected cells independently of proteasome inhibition and interacts with chromatin

A. Mangé, S. Lehmann, C. Crozet, 2004, Journal of Cell Science.

Cell-based therapy against prion diseases.

S. Lehmann, C. Crozet, A. Relaño-Ginés, 2019, Current opinion in pharmacology.

Prion Replication Occurs in Endogenous Adult Neural Stem Cells and Alters Their Neuronal Fate: Involvement of Endogenous Neural Stem Cells in Prion Diseases

A. Gabelle, S. Lehmann, C. Crozet, 2013, PLoS pathogens.

Cerebrospinal fluid anti-cerebellar soluble lectin antibodies in human immunodeficiency virus type 1 infection

G. Norkrans, L. Hagberg, S. Lehmann, 1992, Journal of Neuroimmunology.

Blockade of Glycosylation Promotes Acquistion of Scrapie-like Properties by the Prion Protein in Cultured Cells*

D. Harris, S. Lehmann, 1997, The Journal of Biological Chemistry.

Oxidative stress and the prion protein in transmissible spongiform encephalopathies

S. Lehmann, O. Milhavet, 2002, Brain Research Reviews.

Lithium as a disease-modifying agent for prion diseases

S. Lehmann, C. Crozet, A. Relaño-Ginés, 2018, Translational Psychiatry.

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

M. D. Di Bari, R. Nonno, S. Lehmann, 2021, Scientific Reports.

Recombinant Human Prion Protein Inhibits Prion Propagation in vitro

J. Steyaert, J. Castilla, W. Surewicz, 2013, Scientific Reports.

Signal transduction through prion protein.

J. Laplanche, J. Launay, M. Ermonval, 2000, Science.

Screening of 145 Anti-PrP Monoclonal Antibodies for Their Capacity to Inhibit PrPSc Replication in Infected Cells*

S. Simon, N. Morel, J. Grassi, 2005, Journal of Biological Chemistry.

Prion propagation in cultured cells.

J. Solassol, S. Lehmann, C. Crozet, 2003, British medical bulletin.

Cellular pathogenesis in prion diseases.

S. Lehmann, C. Crozet, F. Béranger, 2008, Veterinary research.

Prion strains are differentially released through the exosomal pathway

G. Raposo, P. Leblanc, O. Andréoletti, 2015, Cellular and Molecular Life Sciences.

An endogenous lectin and one of its neuronal glycoprotein ligands are involved in contact guidance of neuron migration.

S. Lehmann, G. Vincendon, J. Zanetta, 1990, Proceedings of the National Academy of Sciences of the United States of America.

Effect of Congo Red on Wild‐Type and Mutated Prion Proteins in Cultured Cells

A. Mangé, S. Lehmann, D. Casanova, 2000, Journal of neurochemistry.

[Cell culture models of transmissible spongiform encephalopathies].

J. Solassol, A. Mangé, H. Laude, 2001, Comptes rendus biologies.

Effect of Amphotericin B on Wild‐Type and Mutated Prion Proteins in Cultured Cells

A. Mangé, S. Lehmann, H. E. McMahon, 2000, Journal of neurochemistry.

Cell biology of the prion protein.

K. Moulder, D. Harris, S. Shyng, 1996, Current topics in microbiology and immunology.

Successful Transmission of Three Mouse-Adapted Scrapie Strains to Murine Neuroblastoma Cell Lines Overexpressing Wild-Type Mouse Prion Protein

D. Harris, H. Laude, J. Grassi, 2000, Journal of Virology.

Inhibition of PrPSc formation by lentiviral gene transfer of PrP containing dominant negative mutations

S. Lehmann, V. Perrier, Yea-Lih Lin, 2004, Journal of Cell Science.

Ex vivo propagation of infectious sheep scrapie agent in heterologous epithelial cells expressing ovine prion protein

O. Andréoletti, H. Laude, S. Lehmann, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Efficient inhibition of infectious prions multiplication and release by targeting the exosomal pathway

L. Schaeffer, G. Raposo, P. Leblanc, 2015, Cellular and Molecular Life Sciences.

Retrovirus infection strongly enhances scrapie infectivity release in cell culture

G. Raposo, J. Darlix, P. Leblanc, 2006, The EMBO journal.

Filipin Prevents Pathological Prion Protein Accumulation by Reducing Endocytosis and Inducing Cellular PrP Release*

J. Grassi, S. Lehmann, J. Chabry, 2002, The Journal of Biological Chemistry.

Quiescin-sulfhydryl oxidase inhibits prion formation in vitro

J. Steyaert, R. Petersen, S. Lehmann, 2016, Aging.

The truncated 23-230 form of the prion protein localizes to the nuclei of inducible cell lines independently of its nuclear localization signals and is not cytotoxic

T. Onodera, S. Lehmann, C. Crozet, 2006, Molecular and Cellular Neuroscience.

The Role of the Prion Protein in the Molecular Basis for Synaptic Plasticity and Nervous System Development

R. Zahn, S. Lehmann, S. Encalada, 2007, Journal of Molecular Neuroscience.

Expression of Prion Protein Increases Cellular Copper Binding and Antioxidant Enzyme Activities but Not Copper Delivery*

A. Favier, H. Laude, W. Rachidi, 2003, The Journal of Biological Chemistry.

Genetic heterogeneity versus molecular analysis of prion susceptibility in neuroblasma N2a sublines

J. Laplanche, M. Stern, N. Sevenet, 2008, Archives of Virology.

Production of a monoclonal antibody, against human α-synuclein, in a subpopulation of C57BL/6J mice, presenting a deletion of the α-synuclein locus

J. Pin, S. Lehmann, O. Milhavet, 2010, Journal of Neuroscience Methods.

Cerebellar lectins.

S. Lehmann, P. Dufourcq, G. Vincendon, 1992, International Review of Cytology.

Endogenous mannose-binding lectins in brain development and function

S. Lehmann, G. Vincendon, J. Zanetta, 1991 .

Antibodies to cerebellar soluble lectin CSL in multiple sclerosis

L. Rumbach, S. Lehmann, C. Tranchant, 1990, The Lancet.

Location of a transiently expressed glycoprotein in developing cerebellum delineating its possible ontogenetic roles

G. Rougon, S. Lehmann, G. Vincendon, 1989, Neuroscience.

Techniques in Prion Research

J. Grassi, S. Lehmann, 2004, Methods and Tools in Biosciences and Medicine.

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

V. Béringue, S. Lehmann, J. Coste, 2016, PloS one.

Prion Protein Expression and Processing in Human Mononuclear Cells: The Impact of the Codon 129 Prion Gene Polymorphism

S. Lehmann, J. Coste, C. Segarra, 2009, PloS one.

Anti‐PrP antibodies block PrPSc replication in prion‐infected cell cultures by accelerating PrPC degradation

J. Solassol, J. Grassi, S. Lehmann, 2004, Journal of neurochemistry.

Two mutant prion proteins expressed in cultured cells acquire biochemical properties reminiscent of the scrapie isoform.

D. Harris, S. Lehmann, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Prion diseases and adult neurogenesis: How do prions counteract the brain's endogenous repair machinery?

S. Lehmann, C. Crozet, A. Relaño-Ginés, 2014, Prion.

Isolation of Exosomes and Microvesicles from Cell Culture Systems to Study Prion Transmission.

L. Schaeffer, G. Raposo, P. Leblanc, 2017, Methods in molecular biology.

Proteomic consequences of expression and pathological conversion of the prion protein in inducible neuroblastoma N2a cells

O. Windl, P. Leblanc, S. Lehmann, 2010, Prion.

Biological and Biochemical Characteristics of Prion Strains Conserved in Persistently Infected Cell Cultures

S. Lehmann, S. Katamine, N. Kobayashi, 2005, Journal of Virology.

Presence of anti-CSL antibodies in the cerebrospinal fluid of patients: A sensitive and specific test in the diagnosis of multiple sclerosis

J. Warter, S. Lehmann, S. Kuchler-Bopp, 1994, Journal of Neuroimmunology.

Neural Stem Cell Model for Prion Propagation

R. McKay, S. Lehmann, O. Milhavet, 2006, Stem cells.

160 Mutant prion proteins acquire PrP5c-like properties in cultured cells: an experimental model of familial prion diseases

D. Harris, S. Lehmann, 1996, Neurobiology of Aging.

Cationic phosphorus-containing dendrimers reduce prion replication both in cell culture and in mice infected with scrapie.

J. Solassol, D. Dormont, A. Caminade, 2004, The Journal of general virology.

A new genetic algorithm in proteomics: Feature selection for SELDI-TOF data

Nicolas Molinari, Robert Sabatier, Christelle Reynès, 2008, Comput. Stat. Data Anal..

HEPES inhibits the conversion of prion protein in cell culture.

S. Lehmann, O. Milhavet, D. Casanova, 2011, The Journal of general virology.

Brain Lectins:Structure and Function.

S. Lehmann, P. Dufourcq, J. Zanetta, 1992 .