Prion Propagation and Toxicity Occur In Vitro with Two-Phase Kinetics Specific to Strain and Neuronal Type

Por Hannaoui, Samia, Maatouk, Layal, Privat, Nicolas, Levavasseur, Etienne, Faucheux, Baptiste A., Haïk, Stéphane
Publicado em 2013

Accelerated, Spleen-Based Titration of Variant Creutzfeldt-Jakob Disease Infectivity in Transgenic Mice Expressing Human Prion Protein with Sensitivity Comparable to That of Surviv...

Por Halliez, Sophie, Reine, Fabienne, Herzog, Laetitia, Jaumain, Emilie, Haïk, Stéphane, Rezaei, Human, Vilotte, Jean-Luc, Laude, Hubert, Béringue, Vincent
Publicado em 2014

Molecular Modeling of Prion Transmission to Humans

Por Levavasseur, Etienne, Privat, Nicolas, Martin, Juan-Carlos Espinosa, Simoneau, Steve, Baron, Thierry, Flan, Benoit, Torres, Juan-Maria, Haïk, Stéphane
Publicado em 2014

Region-specific protein misfolding cyclic amplification reproduces brain tropism of prion strains

Por Privat, Nicolas, Levavasseur, Etienne, Yildirim, Serfildan, Hannaoui, Samia, Brandel, Jean-Philippe, Laplanche, Jean-Louis, Béringue, Vincent, Seilhean, Danielle, Haïk, Stéphane
Publicado no J Biol Chem (2017)

Absence of Evidence for a Causal Link between Bovine Spongiform Encephalopathy Strain Variant L-BSE and Known Forms of Sporadic Creutzfeldt-Jakob Disease in Human PrP Transgenic Mi...

Por Jaumain, Emilie, Quadrio, Isabelle, Herzog, Laetitia, Reine, Fabienne, Rezaei, Human, Andréoletti, Olivier, Laude, Hubert, Perret-Liaudet, Armand, Haïk, Stéphane, Béringue, Vincent
Publicado no J Virol (2016)

Prominent and Persistent Extraneural Infection in Human PrP Transgenic Mice Infected with Variant CJD

Por Béringue, Vincent, Le Dur, Annick, Tixador, Philippe, Reine, Fabienne, Lepourry, Laurence, Perret-Liaudet, Armand, Haïk, Stéphane, Vilotte, Jean-Luc, Fontés, Michel, Laude, Hubert
Publicado em 2008

Accuracy of diagnosis criteria in patients with suspected diagnosis of sporadic Creutzfeldt-Jakob disease and detection of 14-3-3 protein, France, 1992 to 2009

Por Peckeu, Laurene, Delasnerie-Lauprètre, Nicole, Brandel, Jean-Philippe, Salomon, Dominique, Sazdovitch, Véronique, Laplanche, Jean-Louis, Duyckaerts, Charles, Seilhean, Danielle, Haïk, Stéphane, Hauw, Jean-Jacques
Publicado no Euro Surveill (2017)

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

Por Gauczynski, Sabine, Peyrin, Jean-Michel, Haïk, Stéphane, Leucht, Christoph, Hundt, Christoph, Rieger, Roman, Krasemann, Susanne, Deslys, Jean-Philippe, Dormont, Dominique, Lasmézas, Corinne Ida, Weiss, Stefan
Publicado em 2001

Regulating Factors of PrP(res) Glycosylation in Creutzfeldt-Jakob Disease - Implications for the Dissemination and the Diagnosis of Human Prion Strains

Por Levavasseur, Etienne, Laffont-Proust, Isabelle, Morain, Émilie, Faucheux, Baptiste A., Privat, Nicolas, Peoc'h, Katell, Sazdovitch, Véronique, Brandel, Jean-Philippe, Hauw, Jean-Jacques, Haïk, Stéphane
Publicado em 2008

Correction: Regulating Factors of PrP(res) Glycosylation in Creutzfeldt-Jakob Disease - Implications for the Dissemination and the Diagnosis of Human Prion Strains

Por Levavasseur, Etienne, Laffont-Proust, Isabelle, Morain, Émilie, Faucheux, Baptiste A., Privat, Nicolas, Peoc'h, Katell, Sazdovitch, Véronique, Brandel, Jean-Philippe, Hauw, Jean-Jacques, Haïk, Stéphane
Publicado em 2008

Detection and partial discrimination of atypical and classical bovine spongiform encephalopathies in cattle and primates using real-time quaking-induced conversion assay

Por Levavasseur, Etienne, Biacabe, Anne-Gaëlle, Comoy, Emmanuel, Culeux, Audrey, Grznarova, Katarina, Privat, Nicolas, Simoneau, Steve, Flan, Benoit, Sazdovitch, Véronique, Seilhean, Danielle, Baron, Thierry, Haïk, Stéphane
Publicado no PLoS One (2017)

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

Por Hundt, Christoph, Peyrin, Jean-Michel, Haïk, Stéphane, Gauczynski, Sabine, Leucht, Christoph, Rieger, Roman, Riley, Maria Louise, Deslys, Jean-Philippe, Dormont, Dominique, Lasmézas, Corinne Ida, Weiss, Stefan
Publicado em 2001

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

Por Comoy, Emmanuel E., Mikol, Jacqueline, Jaffré, Nina, Lebon, Vincent, Levavasseur, Etienne, Streichenberger, Nathalie, Sumian, Chryslain, Perret-Liaudet, Armand, Eloit, Marc, Andreoletti, Olivier, Haïk, Stéphane, Hantraye, Philippe, Deslys, Jean-Philippe
Publicado no Nat Commun (2017)

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

Por Vanni, Silvia, Zattoni, Marco, Moda, Fabio, Giaccone, Giorgio, Tagliavini, Fabrizio, Haïk, Stéphane, Deslys, Jean-Philippe, Zanusso, Gianluigi, Ironside, James W., Carmona, Margarita, Ferrer, Isidre, Kovacs, Gabor G., Legname, Giuseppe
Publicado no Front Neurosci (2018)

Prions in the Urine of Patients with Variant Creutzfeldt–Jakob Disease

Por Moda, Fabio, Gambetti, Pierluigi, Notari, Silvio, Concha-Marambio, Luis, Catania, Marcella, Park, Kyung-Won, Maderna, Emanuela, Suardi, Silvia, Haïk, Stéphane, Brandel, Jean-Philippe, Ironside, James, Knight, Richard, Tagliavini, Fabrizio, Soto, Claudio
Publicado em 2014

Constant Transmission Properties of Variant Creutzfeldt-Jakob Disease in 5 Countries

Por Diack, Abigail B., Ritchie, Diane, Bishop, Matthew, Pinion, Victoria, Brandel, Jean-Philippe, Haik, Stephane, Tagliavini, Fabrizio, Van Duijn, Cornelia, Belay, Ermias D., Gambetti, Pierluigi, Schonberger, Lawrence B., Piccardo, Pedro, Will, Robert G., Manson, Jean C.
Publicado em 2012

Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease

Por Xiao, Xiangzhu, Yuan, Jue, Haïk, Stéphane, Cali, Ignazio, Zhan, Yian, Moudjou, Mohammed, Li, Baiya, Laplanche, Jean-Louis, Laude, Hubert, Langeveld, Jan, Gambetti, Pierluigi, Kitamoto, Tetsuyuki, Kong, Qingzhong, Brandel, Jean-Philippe, Cobb, Brian A., Petersen, Robert B., Zou, Wen-Quan
Publicado em 2013

Correction: Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease

Por Xiao, Xiangzhu, Yuan, Jue, Haïk, Stéphane, Cali, Ignazio, Zhan, Yian, Moudjou, Mohammed, Li, Baiya, Laplanche, Jean-Louis, Laude, Hubert, Langeveld, Jan, Gambetti, Pierluigi, Kitamoto, Tetsuyuki, Kong, Qingzhong, Brandel, Jean-Philippe, Cobb, Brian A., Petersen, Robert B., Zou, Wen-Quan
Publicado em 2013

Beyond PrP(res) Type 1/Type 2 Dichotomy in Creutzfeldt-Jakob Disease

Por Uro-Coste, Emmanuelle, Cassard, Hervé, Simon, Stéphanie, Lugan, Séverine, Bilheude, Jean-Marc, Perret-Liaudet, Armand, Ironside, James W., Haik, Stéphane, Basset-Leobon, Christelle, Lacroux, Caroline, Peoch', Katell, Streichenberger, Nathalie, Langeveld, Jan, Head, Mark W., Grassi, Jacques, Hauw, Jean-Jacques, Schelcher, Francois, Delisle, Marie Bernadette, Andréoletti, Olivier
Publicado em 2008

Cerebrospinal fluid real‐time quaking‐induced conversion is a robust and reliable test for sporadic creutzfeldt–jakob disease: An international study

Por McGuire, Lynne I., Poleggi, Anna, Poggiolini, Ilaria, Suardi, Silvia, Grznarova, Katarina, Shi, Song, de Vil, Bart, Sarros, Shannon, Satoh, Katsuya, Cheng, Keding, Cramm, Maria, Fairfoul, Graham, Schmitz, Matthias, Zerr, Inga, Cras, Patrick, Equestre, Michele, Tagliavini, Fabrizio, Atarashi, Ryuichiro, Knox, David, Collins, Steven, Haïk, Stéphane, Parchi, Piero, Pocchiari, Maurizio, Green, Alison
Publicado no Ann Neurol (2016)