Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sebastiaan J van Kampen"'
Autor:
Sebastiaan J. van Kampen, Su Ji Han, Willem B. van Ham, Eirini Kyriakopoulou, Elizabeth W. Stouthart, Birgit Goversen, Jantine Monshouwer-Kloots, Ilaria Perini, Hesther de Ruiter, Petra van der Kraak, Aryan Vink, Linda W. van Laake, Judith A. Groeneweg, Teun P. de Boer, Hoyee Tsui, Cornelis J. Boogerd, Toon A.B. van Veen, Eva van Rooij
Publikováno v:
Stem Cell Reports. 18:749-764
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee9731983c42617636e28f39b28b5143
https://doi.org/10.1016/j.stemcr.2023.01.015
https://doi.org/10.1016/j.stemcr.2023.01.015
Autor:
Loknath Gidijala, Stefan Uthoff, Sebastiaan J. van Kampen, Alexander Steinbüchel, Raymond M. D. Verhaert
Publikováno v:
Microbial Cell Factories, Vol 17, Iss 1, Pp 1-11 (2018)
Abstract Background The yeast Komagataella phaffii, better known as Pichia pastoris, is a commonly used host for recombinant protein production. Here expression vectors are reported that address the different steps of the transcription–translation
Externí odkaz:
https://doaj.org/article/8ec521d7dd704f9ba80f59a964c21571
Autor:
Monika M Gladka, Anne Katrine Z Johansen, Sebastiaan J van Kampen, Marijn M C Peters, Bas Molenaar, Danielle Versteeg, Lieneke Kooijman, Lorena Zentilin, Mauro Giacca, Eva van Rooij
Publikováno v:
Cardiovascular research, 119(3), 802-812. Oxford University Press
Cardiovascular Research. Oxford University Press
Cardiovascular Research. Oxford University Press
Aims The adult mammalian heart is a post-mitotic organ. Even in response to necrotic injuries, where regeneration would be essential to reinstate cardiac structure and function, only a minor percentage of cardiomyocytes undergo cytokinesis. The gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d4440047e77d58b6abb3ad8db3a833d
https://doi.org/10.1093/cvr/cvac155
https://doi.org/10.1093/cvr/cvac155
Autor:
Cornelis J Boogerd, Grégory P A Lacraz, Ábel Vértesy, Sebastiaan J van Kampen, Ilaria Perini, Hesther de Ruiter, Danielle Versteeg, Andreas Brodehl, Petra van der Kraak, Mauro Giacca, Nicolaas de Jonge, Jan Philipp Junker, Alexander van Oudenaarden, Aryan Vink, Eva van Rooij
Publikováno v:
Cardiovascular Research. Oxford University Press
Aims Arrhythmogenic cardiomyopathy (ACM) is an inherited cardiac disorder that is characterized by progressive loss of myocardium that is replaced by fibro-fatty cells, arrhythmias, and sudden cardiac death. While myocardial degeneration and fibro-fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cb1a73dcfa64ab9ef09d4f03d0a95fb
https://doi.org/10.1093/cvr/cvac072
https://doi.org/10.1093/cvr/cvac072
Autor:
Tara Moens, Cornelis J. Boogerd, Eva van Rooij, Marie-José Goumans, Martijn Wehrens, Sebastiaan J. van Kampen, Arwa Kohela, Anke M. Smits, Bas Molenaar, Jantine Monshouwer-Kloots, J. Peter van Tintelen, Ilaria Perini
Publikováno v:
Science Translational Medicine, 13(612). AMER ASSOC ADVANCEMENT SCIENCE
Science Translational Medicine, 13(612). American Association for the Advancement of Science (AAAS)
Science Translational Medicine, 13(612). American Association for the Advancement of Science (AAAS)
Arrhythmogenic cardiomyopathy (ACM) is an inherited disorder often caused by pathogenic variants in desmosomal genes and characterized by progressive fibrotic and fat tissue accumulation in the heart. The cellular origin and responsible molecular mec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f97536b366756c6d26b96926339a355
http://hdl.handle.net/1887/3276198
http://hdl.handle.net/1887/3276198
Autor:
Tara Moens, Arjan Vink, Sebastiaan J. van Kampen, Bas Molenaar, Jantine Monshouwer-Kloots, Eva van Rooij, Martijn Wehrens, Huei-Sheng Vincent Chen, Arwa Kohela
Publikováno v:
Circulation Research. 125
Arrhythmogenic cardiomyopathy (ACM) is an inherited disease mainly caused by desmosomal gene mutations and characterized by myocardial loss, replacement with fibro-fatty tissue, arrhythmias and sudden cardiac death. To date, it is unclear which cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ad0f2180d74d7d0585cd64ea803ddf2
https://doi.org/10.1161/res.125.suppl_1.783
https://doi.org/10.1161/res.125.suppl_1.783
Autor:
Sebastiaan J. van Kampen, J. E. C. Eding, Toon A.B. van Veen, Teun P. de Boer, Eva van Rooij, Eirini Kyriakopoulou, Su Ji Han, Birgit Goversen, Jantine Monshouwer-Kloots
Publikováno v:
Circulation Research. 125
Genetic alterations in desmosomal genes are associated with arrhythmogenic cardiomyopathy (ACM). This condition is characterized by sudden cardiac death, severe arrhythmias, and the presence of fibro-fatty patches within the myocardium. Despite the f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c58d1b689a24de079850d1374cd287f
https://doi.org/10.1161/res.125.suppl_1.786
https://doi.org/10.1161/res.125.suppl_1.786