Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Katarzyna, Hackert"'
Autor:
Florian Funk, Annette Kronenbitter, Katarzyna Hackert, Matthias Oebbeke, Gerhard Klebe, Mareike Barth, Daniel Koch, Joachim P Schmitt
Publikováno v:
Cardiovascular Research
Cardiovascular research 119(7), 1568-1582 (2023). doi:10.1093/cvr/cvad037
Cardiovascular research 119(7), 1568-1582 (2023). doi:10.1093/cvr/cvad037
Cardiovascular research (2023). doi:10.1093/cvr/cvad037
Published by Oxford University Press, Oxford
Published by Oxford University Press, Oxford
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22f61f5c2d92da896dd421fb8963ebf4
https://hdl.handle.net/21.11116/0000-000D-6B09-2
https://hdl.handle.net/21.11116/0000-000D-6B09-2
Autor:
Maria Grandoch, Simone Gorreßen, Florian Funk, Jens W. Fischer, Shakila Mir, Susanne Homann, Joachim P. Schmitt, Arne Beran, Katarzyna Hackert
Publikováno v:
Hypertension
Cardiac wall stress induces local and systemic inflammatory responses that are increasingly recognized as key modulators of extracellular matrix remodeling. Hyaluronic acid interacts with immune cells and mesenchymal cells thereby modulating profibro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48550197f77c97b241092a10e529d70b
https://doi.org/10.1161/hypertensionaha.120.15247
https://doi.org/10.1161/hypertensionaha.120.15247
Autor:
Dennis Glaser, Malgorzata Isić, Simone Gorreßen, Florian Funk, Peter Boknik, Katarzyna Hackert, Joachim P. Schmitt, Kai Stühler, Annette Kronenbitter, Martina Krüger, Gereon Poschmann
Publikováno v:
Journal of Molecular and Cellular Cardiology. 119:28-39
Changes in the nonischemic remote myocardium of the heart contribute to left ventricular dysfunction after ischemia and reperfusion (I/R). Understanding the underlying mechanisms early after I/R is crucial to improve the adaptation of the viable myoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f0262463de60ac0bb30537b54ba9f33
https://doi.org/10.1016/j.yjmcc.2018.04.004
https://doi.org/10.1016/j.yjmcc.2018.04.004
Autor:
Annette, Kronenbitter, Florian, Funk, Katarzyna, Hackert, Simone, Gorreßen, Dennis, Glaser, Peter, Boknik, Gereon, Poschmann, Kai, Stühler, Malgorzata, Isić, Martina, Krüger, Joachim P, Schmitt
Publikováno v:
Journal of molecular and cellular cardiology. 121
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fc6c70ff9a82dc8e68db99b01d11f9be
https://pubmed.ncbi.nlm.nih.gov/29674140
https://pubmed.ncbi.nlm.nih.gov/29674140
Autor:
Annette, Kronenbitter, Florian, Funk, Katarzyna, Hackert, Simone, Gorreßen, Dennis, Glaser, Peter, Boknik, Gereon, Poschmann, Kai, Stühler, Malgorzata, Isić, Martina, Krüger, Joachim P, Schmitt
Publikováno v:
Journal of molecular and cellular cardiology. 119
Changes in the nonischemic remote myocardium of the heart contribute to left ventricular dysfunction after ischemia and reperfusion (I/R). Understanding the underlying mechanisms early after I/R is crucial to improve the adaptation of the viable myoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6b7022803eb71fe1a9dd8b2f4910f346
https://pubmed.ncbi.nlm.nih.gov/29907408
https://pubmed.ncbi.nlm.nih.gov/29907408
Autor:
Malgorzata Isić, Simone Gorreßen, Martina Krüger, Gereon Poschmann, Florian Funk, Joachim P. Schmitt, Katarzyna Hackert, Kai Stühler, Peter Boknik, Dennis Glaser, Annette Kronenbitter
Publikováno v:
Journal of Molecular and Cellular Cardiology. 121:304
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50501ba850d23da42d5e1b3c03e3bcdc
https://doi.org/10.1016/j.yjmcc.2018.06.004
https://doi.org/10.1016/j.yjmcc.2018.06.004
Autor:
Christine E. Seidman, Katarzyna Hackert, Robert Blankenburg, Jon G. Seidman, Sebastian Wurster, René Deenen, Joachim P. Schmitt, Martin J. Lohse
Rationale : Approximately 40% of hypertrophic cardiomyopathy (HCM) is caused by heterozygous missense mutations in β-cardiac myosin heavy chain (β-MHC). Associating disease phenotype with mutation is confounded by extensive background genetic and l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fd84418dae4c3d60108c40bdad2caef
https://europepmc.org/articles/PMC4086907/
https://europepmc.org/articles/PMC4086907/