Cell-specific localization of the sulphydryl oxidase QSOX in rat peripheral tissues

Autor: Béatrice Benayoun, Anna Tury, Georges Mairet-Coello, Pierre-Yves Risold, Dominique Fellmann, B. Griffond, Annick Esnard-Fève

Publikováno v: Cell and Tissue Research
Cell and Tissue Research, Springer Verlag, 2006, 323 (1), pp.91-103. ⟨10.1007/s00441-005-0043-x⟩

International audience; Rat quiescin/sulphydryl oxidase (rQSOX) introduces disulphide bridges into peptides and proteins with the reduction of molecular oxygen to hydrogen peroxide. Its occurrence has been previously highlighted in a wide range of or

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e0c1c7d1c07ed0747065c0d184f6d56
https://doi.org/10.1007/s00441-005-0043-x

NF-kappa B-dependent expression of the antiapoptotic factor c-FLIP is regulated by calpain 3, the protein involved in limb-girdle muscular dystrophy type 2A

Autor: Marc Bartoli, Gérard Lefranc, Nathalie Daniele, Alicia Lajmanovich, Laurence Suel, Béatrice Benayoun, Hanns Lochmüller, Nathalie Bourg, Marie-Anne Pasquier, Stephen Baghdiguian, Isabelle Richard, Evelyne Gicquel, Fabrice Raynaud

Publikováno v: FASEB Journal
FASEB Journal, Federation of American Society of Experimental Biology, 2008, 22 (5), pp.1521-1529. ⟨10.1096/fj.07-8701com⟩
FASEB Journal, 2008, 22 (5), pp.1521-1529. ⟨10.1096/fj.07-8701com⟩

International audience; Limb-girdle muscular dystrophy type 2A (LGMD2A) is a recessive genetic disorder caused by mutations in the cysteine protease calpain 3 (CAPN3) that leads to selective muscle wasting. We previously showed that CAPN3 deficiency

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::821ddb409961663a9201b70bc0e98950
https://hal.archives-ouvertes.fr/hal-01610041