Zobrazeno 1 - 10
of 219
pro vyhledávání: '"B. van Veen"'
Autor:
S. M. Kamel, C. J. M. van Opbergen, C. D. Koopman, A. O. Verkerk, B. J. D. Boukens, B. de Jonge, Y. L. Onderwater, E. van Alebeek, S. Chocron, C. Polidoro Pontalti, W. J. Weuring, M. A. Vos, T. P. de Boer, T. A. B. van Veen, J. Bakkers
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-15 (2021)
Arrhythmogenic cardiomyopathy is a genetically inherited disease caused by deletion of an arginine in Phospholamban (PLN), a small protein that regulates intracellular calcium levels. Here the authors show that zebrafish with the PLN p.Arg14del mutat
Externí odkaz:
https://doaj.org/article/3fe9035389c84ef186c3c9c4ea25cda4
Autor:
Willem B. van Ham, Esmeralda E. M. Meijboom, Merel L. Ligtermoet, Peter G. J. Nikkels, Toon A. B. van Veen
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 10, Iss 8, p 354 (2023)
The development of the normal human heart, ranging from gestational age to the mature adult heart, relies on a very delicate and timely orchestrated order of processes. One of the most striking alterations in time is the gradual extinction of the abi
Externí odkaz:
https://doaj.org/article/54e18138646b4512814ae4be390912db
Autor:
Stephanie M. van der Voorn, Mimount Bourfiss, Anneline S. J. M. te Riele, Karim Taha, Marc A. Vos, Remco de Brouwer, Tom E. Verstraelen, Rudolf A. de Boer, Carol Ann Remme, Toon A. B. van Veen
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2022)
Background: Pathogenic variants in phospholamban (PLN, like p. Arg14del), are found in patients diagnosed with arrhythmogenic (ACM) and dilated cardiomyopathy (DCM). Fibrosis formation in the heart is one of the hallmarks in PLN p.Arg14del carriers.
Externí odkaz:
https://doaj.org/article/6192dc2f457e4711a5d653f5b6215f1f
Autor:
Stephanie M. van der Voorn, Mimount Bourfiss, Steven A. Muller, Tolga Çimen, Ardan M. Saguner, Firat Duru, Anneline S. J. M. te Riele, Carol Ann Remme, Toon A. B. van Veen
Publikováno v:
Biomedicines, Vol 11, Iss 3, p 813 (2023)
Arrhythmogenic cardiomyopathy (ACM) is a progressive inheritable disease which is characterized by a gradual fibro-(fatty) replacement of the myocardium. Visualization of diffuse and patchy fibrosis patterns is challenging using clinically applied ca
Externí odkaz:
https://doaj.org/article/2101393d438542ce8aba94d19afeb921
Publikováno v:
Physiological Reviews. 103:2271-2319
The intercalated disc (ID) is a highly specialized structure that connects cardiomyocytes via mechanical and electrical junctions. Although described in some detail by light microscopy in the 19th century, it was in 1966 that electron microscopy imag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d328f75521de69897f84c7b3d40eb7c
https://doi.org/10.1152/physrev.00021.2022
https://doi.org/10.1152/physrev.00021.2022
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
Background: Patients with arrhythmogenic cardiomyopathy may suffer from lethal ventricular arrhythmias. Arrhythmogenic cardiomyopathy is predominantly triggered by mutations in plakophilin-2, a key component of cell-to-cell adhesion and calcium cycli
Externí odkaz:
https://doaj.org/article/bcb80fd8383e42678afc85f90beae7ce
Publikováno v:
Biology of Sex Differences, Vol 10, Iss 1, Pp 1-11 (2019)
Abstract Background Cardiovascular diseases (CVDs) culminating into heart failure (HF) are major causes of death in men and women. Prevalence and manifestation, however, differ between sexes, since men mainly present with coronary artery disease (CAD
Externí odkaz:
https://doaj.org/article/5d48a564fb44428e95bd12ccf99fde59
Autor:
Jiong-Wei Wang, Magda S. C. Fontes, Xiaoyuan Wang, Suet Yen Chong, Elise L. Kessler, Ya-Nan Zhang, Judith J. de Haan, Fatih Arslan, Saskia C. A. de Jager, Leo Timmers, Toon A. B. van Veen, Carolyn S. P. Lam, Dominique P. V. de Kleijn
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-10 (2017)
Abstract An involement of Toll-like receptor 2 (TLR2) has been established in cardiac dysfunction after acute myocardial infarction; however, its role in chronic pressure overload is unclear. We sought to evaluate the role of TLR2 in cardiac hypertro
Externí odkaz:
https://doaj.org/article/d91281989b32469aa064567a69b66e0f
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
Arrhythmogenic cardiomyopathy (ACM) is a familial heart disease, associated with ventricular arrhythmias, fibrofatty replacement of the myocardial mass and an increased risk of sudden cardiac death (SCD). Malignant ventricular arrhythmias and SCD lar
Externí odkaz:
https://doaj.org/article/9009373292e346f38c3cc739ee18015d
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