Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Stephanie M. Van der Voorn"'
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
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:
Willem B. van Ham, Carlijn M. Cornelissen, Elizaveta Polyakova, Stephanie M. van der Voorn, Merel L. Ligtermoet, Jantine Monshouwer-Kloots, Marc A. Vos, Alexandre Bossu, Eva van Rooij, Marcel A. G. van der Heyden, Toon A. B. van Veen
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 6; Pages: 5373
Chronic kidney disease (CKD) is represented by a diminished filtration capacity of the kidneys. End-stage renal disease patients need dialysis treatment to remove waste and toxins from the circulation. However, endogenously produced uremic toxins (UT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8e349f9186fb3bbab294b7324b1b359
Autor:
Cristina Basso, Anneline S.J.M. te Riele, Hugh Calkins, Stephanie M. van der Voorn, Toon A.B. van Veen, Carol Ann Remme
Publikováno v:
Cardiovascular Research
Arrhythmogenic cardiomyopathy (ACM) is a life-threatening cardiac disease caused by mutations in genes predominantly encoding for desmosomal proteins that lead to alterations in the molecular composition of the intercalated disc. ACM is characterized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f53d78cdd9b3232fe67accbf26960a13
https://doi.org/10.1093/cvr/cvaa084
https://doi.org/10.1093/cvr/cvaa084
Autor:
Marc A. Vos, Laila El Onsri, Mimount Bourfiss, Toon A.B. van Veen, Stephanie M. van der Voorn, Ferogh Mirzad, Helen E. Driessen, Freyja H.M. van Lint
Publikováno v:
Heart Rhythm. 18:S101-S102
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ccc790861f3ae4df6ff5c098a5057489
https://doi.org/10.1016/j.hrthm.2021.06.273
https://doi.org/10.1016/j.hrthm.2021.06.273
Autor:
Lorenzo Calviello, Chuwen Lin, Brian L. Black, Xuan Jiang, Prajakta Ghatpande, Amit Prabhakar, Wanpeng Wang, Giorgio Lagna, Srivats Venkataramanan, Stephanie M. Van der Voorn, Barbara Celona, Stephen N. Floor, Akiko Hata
Ribosome biogenesis in eukaryotes requires stoichiometric production and assembly of 80 ribosomal proteins (RPs) and 4 ribosomal RNAs, and its rate must be coordinated with cellular growth. The indispensable regulator of RP biosynthesis is the 5’-t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bfe07765dad3d859029cac338af1d08
https://doi.org/10.1101/2020.04.24.060236
https://doi.org/10.1101/2020.04.24.060236
Autor:
Helen E. Driessen, Stephanie M. van der Voorn, Mimount Bourfiss, Freyja H. M. van Lint, Ferogh Mirzad, Laila El Onsri, Marc A. Vos, Toon A. B. van Veen
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 57, p 57 (2022)
International journal of molecular sciences, 23(1):57. Multidisciplinary Digital Publishing Institute (MDPI)
International Journal of Molecular Sciences
International Journal of Molecular Sciences; Volume 23; Issue 1; Pages: 57
International journal of molecular sciences, 23(1):57. Multidisciplinary Digital Publishing Institute (MDPI)
International Journal of Molecular Sciences
International Journal of Molecular Sciences; Volume 23; Issue 1; Pages: 57
In arrhythmogenic cardiomyopathy (ACM) pathogenic variants are found in genes encoding desmosomal proteins and in non-desmosomal genes, such as phospholamban (PLN, p.Arg14del variant). Previous research showed that plakoglobin protein levels and loca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bf90c54e0db7e9c5d618d5dd12a07d3
https://doi.org/10.3390/ijms23010057
https://doi.org/10.3390/ijms23010057
Autor:
Marc A. Vos, Stephanie M. van der Voorn, Toon A.B. van Veen, Teun P. de Boer, Chantal J. M. van Opbergen
Publikováno v:
Progress in Biophysics & Molecular Biology, 45. Elsevier Limited
STARTPAGE=45;ISSN=0079-6107;TITLE=Progress in Biophysics & Molecular Biology
STARTPAGE=45;ISSN=0079-6107;TITLE=Progress in Biophysics & Molecular Biology
Sudden cardiac death is a leading cause of death worldwide, mainly caused by highly disturbed electrical activation patterns in the heart. Currently, murine models are the most popular model to study underlying molecular mechanisms of inherited or ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d3fd466a24d5c507ddc4e0f1a5edd3f
https://dspace.library.uu.nl/handle/1874/375729
https://dspace.library.uu.nl/handle/1874/375729