Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Gunnar Kaiser-Schulz"'
Autor:
Steve Simoneau, Human Rezaei, Nicole Salès, Gunnar Kaiser-Schulz, Maxime Lefebvre-Roque, Catherine Vidal, Jean-Guy Fournier, Julien Comte, Franziska Wopfner, Jeanne Grosclaude, Hermann Schätzl, Corinne Ida Lasmézas
Publikováno v:
PLoS Pathogens, Vol 3, Iss 8, p e125 (2007)
The mechanisms underlying prion-linked neurodegeneration remain to be elucidated, despite several recent advances in this field. Herein, we show that soluble, low molecular weight oligomers of the full-length prion protein (PrP), which possess charac
Externí odkaz:
https://doaj.org/article/b78586e103e84f01b240feec7e8ce3fb
Autor:
Jeanne Grosclaude, Catherine Vidal, Julien Comte, Hermann M. Schätzl, Human Rezaei, Nicole Salès, Franziska Wopfner, Gunnar Kaiser-Schulz, Steve Simoneau, Jean Guy Fournier, Corinne Ida Lasmézas, Maxime Lefebvre-Roque
Publikováno v:
PLoS Pathogens
PLoS Pathogens, 2007, 3 (8), pp.1175-1186. ⟨10.1371/journal.ppat.0030125⟩
PLoS Pathogens, Public Library of Science, 2007, 3 (8), pp.1175-1186. ⟨10.1371/journal.ppat.0030125⟩
Plos Pathogens 8 (3), 1175-1186. (2007)
PLoS Pathogens, Vol 3, Iss 8, p e125 (2007)
PLoS Pathogens, 2007, 3 (8), pp.1175-1186. ⟨10.1371/journal.ppat.0030125⟩
PLoS Pathogens, Public Library of Science, 2007, 3 (8), pp.1175-1186. ⟨10.1371/journal.ppat.0030125⟩
Plos Pathogens 8 (3), 1175-1186. (2007)
PLoS Pathogens, Vol 3, Iss 8, p e125 (2007)
The mechanisms underlying prion-linked neurodegeneration remain to be elucidated, despite several recent advances in this field. Herein, we show that soluble, low molecular weight oligomers of the full-length prion protein (PrP), which possess charac