Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Delphine Bauer"'
Autor:
Adrien Moreau, Jean‐Baptiste Reisqs, Helene Delanoe‐Ayari, Marion Pierre, Alexandre Janin, Antoine Deliniere, Francis Bessière, Albano C. Meli, Azzouz Charrabi, Estele Lafont, Camille Valla, Delphine Bauer, Elodie Morel, Vincent Gache, Gilles Millat, Xavier Nissan, Adele Faucherre, Chris Jopling, Sylvain Richard, Alexandre Mejat, Philippe Chevalier
Publikováno v:
Clinical and Translational Medicine, Vol 11, Iss 3, Pp n/a-n/a (2021)
Abstract Background Severe ventricular rhythm disturbances are the hallmark of arrhythmogenic cardiomyopathy (ACM), and are often explained by structural conduction abnormalities. However, comprehensive investigations of ACM cell electrical instabili
Externí odkaz:
https://doaj.org/article/c9664adcb3fe4088aa3cbb1ca8360b5b
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-16 (2017)
Abstract Since the identification of the first disease causing mutation in the gene coding for emerin, a transmembrane protein of the inner nuclear membrane, hundreds of mutations and variants have been found in genes encoding for nuclear envelope co
Externí odkaz:
https://doaj.org/article/a19f61b0896849b587f51e14fd118592
Publikováno v:
ArchéoSciences. :275-286
Le site de la maison 1 du district de Berg Armo a Sainte-Marie-aux-Mines (Haut-Rhin, France) a permis la mise au jour d’un lot important de ceramique de poele date du xvie siecle. Des analyses physico-chimiques ont ete effectuees sur cet ensemble c
Autor:
Delphine Bauer
Publikováno v:
Cinquante ans de désindustrialisation. :229-235
Autor:
Delphine Bauer
Publikováno v:
Revue d’Alsace. :482-483
Autor:
Pierre Fluck, Delphine Bauer, Jean-François Bouvier, Patrick Clerc, Alexandre Disser, Joseph Gauthier, Émilie Nodot
Publikováno v:
Archéologie médiévale. :349-350
Autor:
Delphine Bauer
Publikováno v:
Archéologie médiévale. :272
Publikováno v:
Archives of Cardiovascular Diseases Supplements. (1):86
Introduction Mutations in the DSC2 gene cause Arrhythmogenic Right Ventricular Dysplasia (ARVD). The mechanisms by which these mutations confer histologic substrate remain unknown. It has been suggested that endogenous caspase-1 activity promotes the