Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Delphine M. Béziau"'
Autor:
C Fauvel, Thierry Le Tourneau, Jean-Jacques Schott, Eric Durand, Hélène Eltchaninoff, Romain Capoulade, Delphine M. Béziau
Publikováno v:
Archives of cardiovascular diseases
Archives of cardiovascular diseases, Elsevier/French Society of Cardiology, 2020, 113 (3), pp.209-221. ⟨10.1016/j.acvd.2019.11.007⟩
Archives of cardiovascular diseases, Elsevier/French Society of Cardiology, 2020, 113 (3), pp.209-221. ⟨10.1016/j.acvd.2019.11.007⟩
Until recently, transcatheter aortic valve implantation was restricted to high-risk and inoperable patients. The updated 2017 European Society of Cardiology Guidelines has widened the indication to include intermediate-risk patients, based on two rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2a6c479ab0546f8aa26ef13b739cb79
https://doi.org/10.1016/j.acvd.2019.11.007
https://doi.org/10.1016/j.acvd.2019.11.007
Autor:
Delphine M Béziau, Fanny Toussaint, Alexandre Blanchette, Nour R Dayeh, Chimène Charbel, Jean-Claude Tardif, Jocelyn Dupuis, Jonathan Ledoux
Publikováno v:
PLoS ONE, Vol 10, Iss 4, p e0123769 (2015)
Phospholipase C (PLC) comprises a superfamily of enzymes that play a key role in a wide array of intracellular signalling pathways, including protein kinase C and intracellular calcium. Thirteen different mammalian PLC isoforms have been identified a
Externí odkaz:
https://doaj.org/article/108cee6842694178a0602809589d023d
Autor:
Marjorie Brand, Eric Durand, Sylvanie Renet, Delphine M. Béziau, Sylvain Fraineau, Julie Rondeaux, Déborah Groussard, Ebba Brakenhielm, Virginie Tardif, Alphonse Chu, Zina Badji, Dominique Guerrot, Jean-Paul Henry, Vincent Richard, Anaïs Dumesnil, Claire Vézier
Epigenetic regulation of histone H3K27 methylation has recently emerged as a key step during alternative M2-like macrophage polarization, essential for cardiac repair after Myocardial Infarction (MI). We hypothesized that EZH2, responsible for H3K27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a02fea2f9f3fc97b963d87f0e88c947
https://doi.org/10.21203/rs.3.rs-263770/v1
https://doi.org/10.21203/rs.3.rs-263770/v1
Autor:
Olivier Barthez, Philippe Charron, Samuel Saal, Jean-Eric Wolf, Rodolphe Turpault, Julien Barc, Gildas Loussouarn, Isabelle Baró, Florence Kyndt, Vincent Probst, Géraldine Bertaux, Mohamed Yassine Amarouch, Estelle Baron, Christel Thauvin-Robinet, Gabriel Laurent, Flavien Charpentier, Delphine M. Béziau, Laurence Faivre, Jean Mérot, Yves Coudière, Véronique Fressart, Christian Dina, Alice Maltret, Elisabeth Villain, Roos F. Marsman, Arthur A.M. Wilde, Jean-Jacques Schott
Publikováno v:
Journal of the American College of Cardiology
OBJECTIVES: The aim of this study was to describe a new familial cardiac phenotype and to elucidate the electrophysiological mechanism responsible for the disease. BACKGROUND: Mutations in several genes encoding ion channels, especially SCN5A, have e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15eee1f2604a91752ebd9d51280c1b05
https://doi.org/10.1016/j.jacc.2012.02.052
https://doi.org/10.1016/j.jacc.2012.02.052
Autor:
Jean-Jacques Schott, Aude Solnon, Simon Lecointe, Patricia Bouillet, Laurianne Le Gloan, Thomas O'Hara, Isabelle Baró, Mohamed Yassine Amarouch, Dominique Pavin, Pascale Guicheney, Hervé Le Marec, Richard Redon, Jean-Baptiste Gourraud, Gildas Loussouarn, Philippe Mabo, Delphine M. Béziau, Isabelle Denjoy, Julien Barc, Florence Kyndt, Vincent Probst
Publikováno v:
Basic Research in Cardiology. 109
Brugada syndrome (BrS) is characterized by ST-segment elevation in the right precordial leads and is associated with increased risk of sudden cardiac death. We have recently reported families with BrS and SCN5A mutations where some affected members d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5372e70e153ea3d2d94b115b7498e75
https://doi.org/10.1007/s00395-014-0446-5
https://doi.org/10.1007/s00395-014-0446-5
Autor:
Julien Barc, Isabelle Baró, Jean-Jacques Schott, Mohamed Yassine Amarouch, Florence Kyndt, Vincent Probst, Delphine M. Béziau, H. Le Marec, D. Babuty
Publikováno v:
Archives of Cardiovascular Diseases. 102
Short QT syndrome (SQTS) emerged as a new inherited channelopathy characterized by constantly short QT interval (QTcC transition caused a p.A223P substitution of a mammalian highly conserved residue. This variant was absent in 312 healthy controls.Ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d64b167ab6a835e4f2fe5fe3142fe6e9
Autor:
Jean Eric Wolf, Isabelle Baró, Rodolphe Turpault, Gildas Loussouarn, Mohamed Yassine Amarouch, Roos F. Marsman, Arthur A.M. Wilde, Samuel Saal, Gabriel Laurent, Alice Maltret, Florence Kyndt, Vincent Probst, Christian Dina, Delphine M. Béziau, Philippe Charron
Publikováno v:
ResearcherID
Using a candidate-gene approach, we detected a variant of SCN5A, encoding the cardiac Na+ channel Nav1.5, by screening a family with cardiac arrhythmia resulting in frequent premature ventricular contractions (PVCs) and non-sustained ventricular tach
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28b41f9de8503029dbe32bf1b043f262