Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Eric Schulze‐Bahr"'
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
BackgroundHypertrophic cardiomyopathy (HCM) is a serious hereditary cardiomyopathy. It is characterized morphologically by an increased left ventricular wall thickness and mass and functionally by enhanced global chamber function and myocellular cont
Externí odkaz:
https://doaj.org/article/c20267dcceb84d2baf026df4e6a9f8cf
Autor:
Greta Marie Pohl, Manuel Göz, Anna Gaertner, Andreas Brodehl, Tolga Cimen, Ardan M. Saguner, Eric Schulze-Bahr, Volker Walhorn, Dario Anselmetti, Hendrik Milting
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
BackgroundArrhythmogenic cardiomyopathy can be caused by genetic variants in desmosomal cadherins. Since cardiac desmosomal cadherins are crucial for cell-cell-adhesion, their correct localization at the plasma membrane is essential.MethodsNine desmo
Externí odkaz:
https://doaj.org/article/9c3c4fa7f44f46cdb70eece237231b8f