Rezultati - Haïk, Stéphane
- Showing 1 - 20 results of 37
- Go to Next Page
-
1
-
2
-
3
Neuron Dysfunction Is Induced by Prion Protein with an Insertional Mutation via a Fyn Kinase and Reversed by Sirtuin Activation in Caenorhabditis elegans od Bizat, Nicolas, Peyrin, Jean-Michel, Haïk, Stephane, Cochois, Véronique, Beaudry, Patrick, Laplanche, Jean-Louis, Néri, Christian
Izdano 2010Text -
4
Accelerated, Spleen-Based Titration of Variant Creutzfeldt-Jakob Disease Infectivity in Transgenic Mice Expressing Human Prion Protein with Sensitivity Comparable to That of Surviv... od Halliez, Sophie, Reine, Fabienne, Herzog, Laetitia, Jaumain, Emilie, Haïk, Stéphane, Rezaei, Human, Vilotte, Jean-Luc, Laude, Hubert, Béringue, Vincent
Izdano 2014Text -
5
-
6
Region-specific protein misfolding cyclic amplification reproduces brain tropism of prion strains od Privat, Nicolas, Levavasseur, Etienne, Yildirim, Serfildan, Hannaoui, Samia, Brandel, Jean-Philippe, Laplanche, Jean-Louis, Béringue, Vincent, Seilhean, Danielle, Haïk, Stéphane
Izdano 2017Text -
7
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... od Jaumain, Emilie, Quadrio, Isabelle, Herzog, Laetitia, Reine, Fabienne, Rezaei, Human, Andréoletti, Olivier, Laude, Hubert, Perret-Liaudet, Armand, Haïk, Stéphane, Béringue, Vincent
Izdano 2016Text -
8
Genetic Testing in Prion Disease: Psychological Consequences of the Decisions to Know or Not to Know od Schwartz, Mathias, Brandel, Jean-Philippe, Babonneau, Marie Lise, Boucher, Christilla, Schaerer, Elodie, Haik, Stephane, Laplanche, Jean Louis, Gargiulo, Marcela, Durr, Alexandra
Izdano 2019Text -
9
Prominent and Persistent Extraneural Infection in Human PrP Transgenic Mice Infected with Variant CJD od Béringue, Vincent, Le Dur, Annick, Tixador, Philippe, Reine, Fabienne, Lepourry, Laurence, Perret-Liaudet, Armand, Haïk, Stéphane, Vilotte, Jean-Luc, Fontés, Michel, Laude, Hubert
Izdano 2008Text -
10
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 od Peckeu, Laurene, Delasnerie-Lauprètre, Nicole, Brandel, Jean-Philippe, Salomon, Dominique, Sazdovitch, Véronique, Laplanche, Jean-Louis, Duyckaerts, Charles, Seilhean, Danielle, Haïk, Stéphane, Hauw, Jean-Jacques
Izdano 2017Text -
11
Transmission of amyloid-beta and tau pathologies is associated with cognitive impairments in a primate od Lam, Suzanne, Petit, Fanny, Hérard, Anne-Sophie, Boluda, Susana, Eddarkaoui, Sabiha, Guillermier, Martine, Buée, Luc, Duyckaerts, Charles, Haïk, Stéphane, Picq, Jean-Luc, Dhenain, Marc
Izdano 2021Text -
12
The 37-kDa/67-kDa laminin receptor acts as the cell-surface receptor for the cellular prion protein od 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
Izdano 2001Text -
13
Regulating Factors of PrP(res) Glycosylation in Creutzfeldt-Jakob Disease - Implications for the Dissemination and the Diagnosis of Human Prion Strains od 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
Izdano 2008Text -
14
Correction: Regulating Factors of PrP(res) Glycosylation in Creutzfeldt-Jakob Disease - Implications for the Dissemination and the Diagnosis of Human Prion Strains od 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
Izdano 2008Text -
15
Detection and partial discrimination of atypical and classical bovine spongiform encephalopathies in cattle and primates using real-time quaking-induced conversion assay od 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
Izdano 2017Text -
16
Identification of interaction domains of the prion protein with its 37-kDa/67-kDa laminin receptor od 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
Izdano 2001Text -
17
Experimental transfusion of variant CJD-infected blood reveals previously uncharacterised prion disorder in mice and macaque od 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
Izdano 2017Text -
18
Hemoglobin mRNA Changes in the Frontal Cortex of Patients with Neurodegenerative Diseases od 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
Izdano 2018Text -
19
Prions in the Urine of Patients with Variant Creutzfeldt–Jakob Disease od 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
Izdano 2014Text -
20
Sensitive protein misfolding cyclic amplification of sporadic Creutzfeldt–Jakob disease prions is strongly seed and substrate dependent od Bélondrade, Maxime, Nicot, Simon, Mayran, Charly, Bruyere-Ostells, Lilian, Almela, Florian, Di Bari, Michele A., Levavasseur, Etienne, Watts, Joel C., Fournier-Wirth, Chantal, Lehmann, Sylvain, Haïk, Stéphane, Nonno, Romolo, Bougard, Daisy
Izdano 2021Text