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Aleksandra Nijak

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Stem Cell Research|March 5, 2022
Generation of two induced pluripotent stem cell (iPSC) lines (BBANTWi006-A, BBANTWi007-A) from Brugada syndrome patients carrying an SCN5A mutationEline Simons, Aleksandra Nijak, Bart Loeys, et al.
International Journal of Molecular Sciences|April 3, 2021
iPSC-Cardiomyocyte Models of Brugada Syndrome-Achievements, Challenges and Future PerspectivesAleksandra Nijak, Johan Saenen, Alain J Labro, et al.
Stem Cell Research|November 10, 2022
Generation of a human TGFB3-hIPSC line, BBANTWi010-A, from a Loeys-Dietz syndrome type V patientMelanie Perik, Aline Verstraeten, Aleksandra Nijak-Paeske, et al.
Stem Cell Research|August 21, 2024
Generation of four distinct isogenic cell lines with truncating variants in I-band or A-band titinHanne M Boen, Bert Vandendriessche, Jolien Schippers, et al.
European Journal of Medical Genetics|October 13, 2017
Left ventricular non-compaction with Ebstein anomaly attributed to a TPM1 mutationAleksandra Nijak, Maaike Alaerts, Cuno Kuiperi, et al.
European Journal of Medical Genetics|August 26, 2021
Molecular autopsy and subsequent functional analysis reveal de novo DSG2 mutation as cause of sudden deathEline Simons, Alain Labro, Johan Saenen, et al.
Orphanet Journal of Rare Diseases|February 1, 2023
Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian populationEwa Sieliwonczyk, Maaike Alaerts, Eline Simons, et al.
Frontiers in Cardiovascular Medicine|August 28, 2020
Compound Heterozygous <i>SCN5A</i> Mutations in Severe Sodium Channelopathy With Brugada Syndrome: A Case ReportAleksandra Nijak, Alain J Labro, Hans De Wilde, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|November 22, 2020
Clinical characterization of the first Belgian SCN5A founder mutation cohortEwa Sieliwonczyk, Maaike Alaerts, Tomas Robyns, et al.
Biology Open|February 23, 2022
Morpho-functional comparison of differentiation protocols to create iPSC-derived cardiomyocytesAleksandra Nijak, Eline Simons, Bert Vandendriessche, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Stem Cell Research|March 5, 2022
Generation of two induced pluripotent stem cell (iPSC) lines (BBANTWi006-A, BBANTWi007-A) from Brugada syndrome patients carrying an SCN5A mutationEline Simons, Aleksandra Nijak, Bart Loeys, et al.
International Journal of Molecular Sciences|April 3, 2021
iPSC-Cardiomyocyte Models of Brugada Syndrome-Achievements, Challenges and Future PerspectivesAleksandra Nijak, Johan Saenen, Alain J Labro, et al.
Stem Cell Research|November 10, 2022
Generation of a human TGFB3-hIPSC line, BBANTWi010-A, from a Loeys-Dietz syndrome type V patientMelanie Perik, Aline Verstraeten, Aleksandra Nijak-Paeske, et al.
Stem Cell Research|August 21, 2024
Generation of four distinct isogenic cell lines with truncating variants in I-band or A-band titinHanne M Boen, Bert Vandendriessche, Jolien Schippers, et al.
European Journal of Medical Genetics|October 13, 2017
Left ventricular non-compaction with Ebstein anomaly attributed to a TPM1 mutationAleksandra Nijak, Maaike Alaerts, Cuno Kuiperi, et al.
European Journal of Medical Genetics|August 26, 2021
Molecular autopsy and subsequent functional analysis reveal de novo DSG2 mutation as cause of sudden deathEline Simons, Alain Labro, Johan Saenen, et al.
Orphanet Journal of Rare Diseases|February 1, 2023
Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian populationEwa Sieliwonczyk, Maaike Alaerts, Eline Simons, et al.
Frontiers in Cardiovascular Medicine|August 28, 2020
Compound Heterozygous <i>SCN5A</i> Mutations in Severe Sodium Channelopathy With Brugada Syndrome: A Case ReportAleksandra Nijak, Alain J Labro, Hans De Wilde, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|November 22, 2020
Clinical characterization of the first Belgian SCN5A founder mutation cohortEwa Sieliwonczyk, Maaike Alaerts, Tomas Robyns, et al.
Biology Open|February 23, 2022
Morpho-functional comparison of differentiation protocols to create iPSC-derived cardiomyocytesAleksandra Nijak, Eline Simons, Bert Vandendriessche, et al.
Pageof 2