Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Ulrike B Esslinger"'
Autor:
Klaus Stark, Ulrike B Esslinger, Wibke Reinhard, George Petrov, Thomas Winkler, Michel Komajda, Richard Isnard, Philippe Charron, Eric Villard, François Cambien, Laurence Tiret, Marie-Claude Aumont, Olivier Dubourg, Jean-Noël Trochu, Laurent Fauchier, Pascal Degroote, Anette Richter, Bernhard Maisch, Thomas Wichter, Christa Zollbrecht, Martina Grassl, Heribert Schunkert, Patrick Linsel-Nitschke, Jeanette Erdmann, Jens Baumert, Thomas Illig, Norman Klopp, H-Erich Wichmann, Christa Meisinger, Wolfgang Koenig, Peter Lichtner, Thomas Meitinger, Arne Schillert, Inke R König, Roland Hetzer, Iris M Heid, Vera Regitz-Zagrosek, Christian Hengstenberg
Publikováno v:
PLoS Genetics, Vol 6, Iss 10, p e1001167 (2010)
Dilated cardiomyopathy (DCM) is a structural heart disease with strong genetic background. Monogenic forms of DCM are observed in families with mutations located mostly in genes encoding structural and sarcomeric proteins. However, strong evidence su
Externí odkaz:
https://doaj.org/article/56e0d4b0c2df4726aa00ecb1f26bdf14
Autor:
Xavier Jouven, Eric Villard, Jean Philippe Empana, Sophie Garnier, François Cambien, Michel Komajda, Richard Isnard, Patrick Lacolley, Claudine Perret, Carole Proust, Ulrike B. Esslinger, Agathe Korniat, Pierre Boutouyrie, Philippe Charron, David-Alexandre Trégouët
Publikováno v:
Printemps de la cardiologie
Printemps de la cardiologie, Apr 2017, Nantes, France
Printemps de la cardiologie, Apr 2017, Nantes, France
Aims Dilated cardiomyopathy (DCM) is an important cause of heart failure with a strong familial component. We performed an exome-wide array-based association study (EWAS) to assess the contribution of missense variants to sporadic DCM. Methods and re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52c084a583a1c0d2cc5b79758b2f5009
https://hal.science/hal-04048876
https://hal.science/hal-04048876
Autor:
Thomas Langmann, Martina Grassl, Regina Höcherl, Christa Zollbrecht, S. Fenk, Ute Hubauer, Wibke Reinhard, Klaus Stark, Stefanie Ebert, Ulrike B. Esslinger, Christian Hengstenberg
Publikováno v:
Atherosclerosis. 227:244-249
Objective Genome-wide association studies identified a risk haplotype on chromosome 9p21.3 to be associated with coronary artery disease (CAD) and myocardial infarction (MI). Since this region does not contain a clear candidate gene with known pathop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::773bbe511817f4e779663c9452b2a42b
https://doi.org/10.1016/j.atherosclerosis.2012.12.030
https://doi.org/10.1016/j.atherosclerosis.2012.12.030
Autor:
François Cambien, Anette Richter, Bernhard Maisch, Christa Zollbrecht, Laurence Tiret, Klaus Stark, Christa Meisinger, Jeanette Erdmann, Thomas Meitinger, Jean-Noël Trochu, Marie-Claude Aumont, Wolfgang Koenig, Laurent Fauchier, Arne Schillert, Peter Lichtner, Martina Grassl, Norman Klopp, Jens Baumert, Iris M. Heid, Vera Regitz-Zagrosek, Pascal DeGroote, Inke R. König, Philippe Charron, Patrick Linsel-Nitschke, Thomas Illig, Eric Villard, Roland Hetzer, Ulrike B. Esslinger, Thomas Wichter, Michel Komajda, Christian Hengstenberg, Thomas W. Winkler, Richard Isnard, Wibke Reinhard, H.-Erich Wichmann, Olivier Dubourg, Heribert Schunkert, George Petrov
Publikováno v:
PLoS Genetics, Vol 6, Iss 10, p e1001167 (2010)
PLoS Genetics
PLoS Genetics, 2010, 6 (10), pp.e1001167. ⟨10.1371/journal.pgen.1001167⟩
Scopus-Elsevier
PLoS Genet. 6:e1001167 (2010)
PLoS Genetics
PLoS Genetics, 2010, 6 (10), pp.e1001167. ⟨10.1371/journal.pgen.1001167⟩
Scopus-Elsevier
PLoS Genet. 6:e1001167 (2010)
Dilated cardiomyopathy (DCM) is a structural heart disease with strong genetic background. Monogenic forms of DCM are observed in families with mutations located mostly in genes encoding structural and sarcomeric proteins. However, strong evidence su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e13bbda5bcabe830059b9dd93e31fee2
http://europepmc.org/articles/PMC2958814?pdf=render
http://europepmc.org/articles/PMC2958814?pdf=render