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pro vyhledávání: '"L. Duboscq-Bidot"'
Akademický článek
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Autor:
Magdalena Harakalova, Benjamin Meder, Philippe Charron, Manuel Gómez-Bueno, Jorg J. A. Calis, François Cambien, David-Alexandre Trégouët, Maurizia Grasso, Steven McGinn, Uwe Völker, Thomas Meitinger, Stefan Weiss, L. Duboscq-Bidot, Richard Dorent, Vera Regitz-Zagrosek, Folkert W. Asselbergs, Hélène Blanché, Olivier Dubourg, Patrick Lacolley, Pierre Boutouyrie, Delphine Bacq-Daian, Vincent Fontaine, Volker Ruppert, Marine Germain, K Lehnert, Jean-Noël Trochu, Stuart A. Cook, Angélique Curjol, Brendan J. Keating, Ibticem Raji, Anne Boland, J. Erdmann, Michael Morley, Jean-François Aupetit, Paloma Remior, Luigi Tavazzi, Gérard Roizès, Michal Mokry, Konstantin Strauch, Richard Isnard, Jean-Philippe Empana, Robert Olaso, Kenneth B. Marguiles, Zofia T. Bilińska, Stephan B. Felix, Marcus Dörr, Thomas P. Cappola, Stefan Blankenberg, Jan Haas, Céline Besse, Jean-François Deleuze, Christine E. Seidman, Christian Hengstenberg, Jessica van Setten, Hakon Hakonarson, Sanjay K Prasad, Daiane Hemerich, Pascal de Groote, Thomas Wichter, Alain van Mil, Michel Komajda, Renee Maas, Carole Proust, Declan P. O'Regan, Xavier Jouven, Ganapathi Varma Saripella, Georgios Kararigas, Eloisa Arbustini, Jin Li, Klaus Stark, Laurent Fauchier, Flavie Ader, Melanie Waldenberger, Martina Müller-Nurasyid, Eric Villard, Sophie Garnier
Publikováno v:
European heart journal, 42(20), 2000-2011. Oxford University Press
European Heart Journal
European Heart Journal, Oxford University Press (OUP): Policy B, 2021, ⟨10.1093/eurheartj/ehab030⟩
European Heart Journal, 2021, 42 (20), pp.2000-2011. ⟨10.1093/eurheartj/ehab030⟩
European Heart Journal
European Heart Journal, Oxford University Press (OUP): Policy B, 2021, ⟨10.1093/eurheartj/ehab030⟩
European Heart Journal, 2021, 42 (20), pp.2000-2011. ⟨10.1093/eurheartj/ehab030⟩
Aims Our objective was to better understand the genetic bases of dilated cardiomyopathy (DCM), a leading cause of systolic heart failure. Methods and results We conducted the largest genome-wide association study performed so far in DCM, with 2719 ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d2fb4a5751c8873677e1b542fdd8c3a
https://pure.amc.nl/en/publications/genomewide-association-analysis-in-dilated-cardiomyopathy-reveals-two-new-players-in-systolic-heart-failure-on-chromosomes-3p251-and-22q1123(8df098a2-4e2b-436a-8594-9c6ed3e705d8).html
https://pure.amc.nl/en/publications/genomewide-association-analysis-in-dilated-cardiomyopathy-reveals-two-new-players-in-systolic-heart-failure-on-chromosomes-3p251-and-22q1123(8df098a2-4e2b-436a-8594-9c6ed3e705d8).html
Autor:
Magdalena Harakalova, François Cambien, David A. Tregouet, Folkert W. Asselbergs, Michal Mokry, P. Charron, Stefan Weiss, Sophie Garnier, J. van Setten, Eric Villard, Jean-François Deleuze, Carole Proust, L. Duboscq-Bidot, Anne Boland, Marcus Dörr
Publikováno v:
European Heart Journal. 41
We conducted the largest Genome Wide Association Study performed so far in Dilated Cardiomyopathy (DCM), a leading cause of systolic heart failure and cardiovascular death. Using a discovery phase of 2,719 cases and 4,440 controls and a replication p
Autor:
M.P. Pruniaux-Harnist, Charlène Jouve, Angélique Curjol, L. Duboscq-Bidot, P. Janiak, P. Charron, Eric Villard, V. Briand, V. Fontaine, J.S. Hulot, M. Hamlin
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 13:206-207
Introduction Hypertrophic cardiomyopathy (HCM) is a relatively frequent (1/500) heart disease that could result in arrhythmia and sudden death. It is mainly caused by sarcomere gene mutations. Disease mechanisms are still poorly known due to limited
Autor:
M. Gizon, L. Duboscq-Bidot, Nathalie Neyroud, Eric Villard, V. Fontaine, L. El Kassa, K. Giraud-Triboult
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 13:232-233
Introduction The cardiac voltage-gated sodium channel α-subunit (Nav1.5), encoded by SCN5A, is a key determinant of cardiac excitability. Variants in SCN5A have been clearly identified as responsible for cardiac arrythmias, highlighting its critical
Autor:
Céline Besse, François Cambien, Folkert W. Asselbergs, Robert Olaso, Jeanette Erdman, Benjamin Meder, Stephan B. Felix, Stefan Weiss, Laurent Fauchier, Konstantin Strauch, Luigi Tavazzi, Anne Boland, Gérard Roizès, Pascal DeGroote, Renee Maas, Melanie Waldenberger, Ganapathi Varma Saripella, Pablo García-Pavía, Brendan J. Keating, Vera Regitz-Zagrosek, Marine Germain, Stefan Blankenberg, Jessica van Setten, Eloisa Arbustini, Pierre Boutouyrie, Carole Proust, Delphine Bacq-Daian, Hemerich Daiane, Sophie Garnier, Michal Mokry, Richard Dorent, Martina Müller-Nurasyid, Philippe Charron, Maurizia Grasso, Steven Mc Ginn, Vincent Fontaine, Uwe Völker, Patrick Lacolley, Thomas Meitinger, Christine E. Seidman, Ibticem Raji, David-Alexandre Trégouët, Jean-Noël Trochu, Thomas Wichter, Jörg Callis, Alain van Mil, Jean-François Deleuze, Declan P. O'Regan, Xavier Jouven, Jin Li, Klaus Stark, Eric Villard, Stuart A. Cook, Hakon Hakonarson, Michael Morley, Kenneth B. Marguiles, Sanjay K Prasad, Volker Ruppert, Jean-François Aupetit, Jean-Philippe Empana, Marcus Dörr, Thomas P. Cappola, Michel Komajda, Magdalena Harakalova, Christian Hengstenberg, Hélène Blanché, Angélique Curjol, L. Duboscq-Bidot, Richard Isnard, Olivier Dubourg, K Lehnert
SummaryWe present the results of the largest genome wide association study (GWAS) performed so far in dilated cardiomyopathy (DCM), a leading cause of systolic heart failure and cardiovascular death, with 2,719 cases and 4,440 controls in the discove
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fc3119dd5f3a16ea14b94c575d999ba
https://doi.org/10.1101/2020.02.28.969147
https://doi.org/10.1101/2020.02.28.969147
Autor:
S. Weiss, David A. Tregouet, Laurent Fauchier, Xavier Jouven, Jean-François Deleuze, Sophie Garnier, Marcus Dörr, Magdalena Harakalova, Jean-Noël Trochu, Richard Dorent, P. De Groote, Michal Mokry, Eric Villard, Olivier Dubourg, P. Charron, François Cambien, Folkert W. Asselbergs, Michel Komajda, L. Duboscq-Bidot, Richard Isnard
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 13:35-36
Background Dilated cardiomyopathy (DCM) is a major cause of systolic heart failure and therefore a major public health issue. Purpose Our objective was to better understand the genetic bases of dilated cardiomyopathy. Methods We conducted a 1000G bas
Autor:
Véronique Briand, Matthieu Hamlin, Eric Villard, Marie-Pierre Pruniaux-Harnist, Philippe Charron, Charlène Jouve, Angélique Curjol, Jean-Sébastien Hulot, Philip Janiak, L. Duboscq-Bidot, Vincent Fontaine
Publikováno v:
Stem Cell Research
Stem Cell Research, Elsevier, 2021, 52, pp.102245. ⟨10.1016/j.scr.2021.102245⟩
Stem Cell Research, Vol 52, Iss, Pp 102245-(2021)
Stem Cell Research, Elsevier, 2021, 52, pp.102245. ⟨10.1016/j.scr.2021.102245⟩
Stem Cell Research, Vol 52, Iss, Pp 102245-(2021)
International audience; MYH7 is a major gene responsible for hypertrophic cardiomyopathy (HCM). From patient’s skin fibroblasts, we derived an iPSC line (CDGEN1.16) harboring the heterozygous MYH7 R403L mutation, a hot-spot codon in HCM. We subsequ
Autor:
Eric Villard, L. Duboscq-Bidot, M. Hamlin, Tiphaine Hery, V. Fontaine, P. Bobin, Estelle Gandjbakhch, P. Charron
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 12:224
Introduction Advances in human induced pluripotent stem cell (hiPSC) technology and the ability to create patient-derived hiPSC lines has raised the possibility for studying pathology-associated specific mutations consequences. However, studies focus
Akademický článek
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