Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Tom Zwetsloot"'
Autor:
Harsha D Devalla, Roselle Gélinas, Elhadi H Aburawi, Abdelaziz Beqqali, Philippe Goyette, Christian Freund, Marie‐A Chaix, Rafik Tadros, Hui Jiang, Antony Le Béchec, Jantine J Monshouwer‐Kloots, Tom Zwetsloot, Georgios Kosmidis, Frédéric Latour, Azadeh Alikashani, Maaike Hoekstra, Jurg Schlaepfer, Christine L Mummery, Brian Stevenson, Zoltan Kutalik, Antoine AF de Vries, Léna Rivard, Arthur AM Wilde, Mario Talajic, Arie O Verkerk, Lihadh Al‐Gazali, John D Rioux, Zahurul A Bhuiyan, Robert Passier
Publikováno v:
EMBO Molecular Medicine, Vol 8, Iss 12, Pp 1390-1408 (2016)
Abstract Genetic causes of many familial arrhythmia syndromes remain elusive. In this study, whole‐exome sequencing (WES) was carried out on patients from three different families that presented with life‐threatening arrhythmias and high risk of
Externí odkaz:
https://doaj.org/article/fbd3c37951794a57a006bfdb37a6a0d0
Autor:
Amer Jamalpoor, Sabine Hartvelt, Myrto Dimopoulou, Tom Zwetsloot, Inger Brandsma, Peter I. Racz, Torben Osterlund, Giel Hendriks
Publikováno v:
Birth Defects Research. 114:1210-1228
Testing for developmental toxicity according to the current regulatory guidelines requires large numbers of animals, making these tests very resource intensive, time-consuming, and ethically debatable. Over the past decades, several alternative in vi
Publikováno v:
Reproductive Toxicology. 88:18-19
Autor:
Tom Zwetsloot, Sarah Williams, Harsha D. Devalla, Sonja Stoelzle-Feix, Ulrich Thomas, Niels Fertig, John Ridley, Said El-Haou, Marc Rogers, Robert Passier, Louise Webdale, Kathy Sutton
Publikováno v:
Journal of Pharmacological and Toxicological Methods, 88(2):0237, 241-241. Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acbb8ac1c85c951d46fbd2fbb42b7105
https://research.utwente.nl/en/publications/human-ventricular-stem-cell-cardiomyocytes-validating-in-vitro-assays-and-screening-platforms-for-proarrhythmia-risk-prediction(e98a16d9-4e17-4aed-858f-ce10eeb6a971).html
https://research.utwente.nl/en/publications/human-ventricular-stem-cell-cardiomyocytes-validating-in-vitro-assays-and-screening-platforms-for-proarrhythmia-risk-prediction(e98a16d9-4e17-4aed-858f-ce10eeb6a971).html
Autor:
Philippe Goyette, Jantine Monshouwer-Kloots, Elhadi H. Aburawi, Marie A. Chaix, Zoltán Kutalik, Arthur A.M. Wilde, Tom Zwetsloot, Brian Stevenson, Azadeh Alikashani, Zahurul A. Bhuiyan, John D. Rioux, Christine L. Mummery, Christian Freund, Jurg Schlaepfer, Robert Passier, Georgios Kosmidis, Hui Jiang, Antoine A.F. de Vries, Abdelaziz Beqqali, Maaike Hoekstra, Arie O. Verkerk, Antony Le Béchec, Rafik Tadros, Mario Talajic, Lihadh Al-Gazali, Lena Rivard, Roselle Gélinas, Harsha D. Devalla, Frédéric Latour
Publikováno v:
EMBO molecular medicine, vol. 8, no. 12, pp. 1390-1408
EMBO molecular medicine, 8(12), 1390-1408. Wiley-Blackwell
Devalla, H D, Gélinas, R, Aburawi, E H, Beqqali, A, Goyette, P, Freund, C, Chaix, M-A, Tadros, R, Jiang, H, Le Béchec, A, Monshouwer-Kloots, J J, Zwetsloot, T, Kosmidis, G, Latour, F, Alikashani, A, Hoekstra, M, Schlaepfer, J, Mummery, C L, Stevenson, B, Kutalik, Z, de Vries, A AF, Rivard, L, Wilde, A AM, Talajic, M, Verkerk, A O, Al-Gazali, L, Rioux, J D, Bhuiyan, Z A & Passier, R 2016, ' TECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT ', EMBO Molecular Medicine, vol. 8, no. 12, pp. 1390-1408 . https://doi.org/10.15252/emmm.201505719
EMBO Molecular Medicine, 8(12), 1390-1408
EMBO Molecular Medicine
EMBO molecular medicine, 8(12), 1390-1408. Wiley-Blackwell
Devalla, H D, Gélinas, R, Aburawi, E H, Beqqali, A, Goyette, P, Freund, C, Chaix, M-A, Tadros, R, Jiang, H, Le Béchec, A, Monshouwer-Kloots, J J, Zwetsloot, T, Kosmidis, G, Latour, F, Alikashani, A, Hoekstra, M, Schlaepfer, J, Mummery, C L, Stevenson, B, Kutalik, Z, de Vries, A AF, Rivard, L, Wilde, A AM, Talajic, M, Verkerk, A O, Al-Gazali, L, Rioux, J D, Bhuiyan, Z A & Passier, R 2016, ' TECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT ', EMBO Molecular Medicine, vol. 8, no. 12, pp. 1390-1408 . https://doi.org/10.15252/emmm.201505719
EMBO Molecular Medicine, 8(12), 1390-1408
EMBO Molecular Medicine
Genetic causes of many familial arrhythmia syndromes remain elusive. In this study, whole‐exome sequencing (WES) was carried out on patients from three different families that presented with life‐threatening arrhythmias and high risk of sudden ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bc321d0326c0649feeedfd6fcc1dde6
https://serval.unil.ch/notice/serval:BIB_EB060DB2BDA6
https://serval.unil.ch/notice/serval:BIB_EB060DB2BDA6