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Aline Verstraeten

Showing results (1-10 of 64) with videos related to

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European Heart Journal|January 18, 2023
The emerging role of endothelial cells in the pathogenesis of thoracic aortic aneurysm and dissectionAline Verstraeten, Ivanna Fedoryshchenko, Bart Loeys
Nature Reviews. Cardiology|January 20, 2017
Aetiology and management of hereditary aortopathyAline Verstraeten, Ilse Luyckx, Bart Loeys
The Journal of Experimental Medicine|April 15, 2020
Hide and seek: Somatic SMAD3 mutations in melorheostosisJoe Davis Velchev, Aline Verstraeten, Bart Loeys
Trends in Genetics : TIG|February 24, 2015
Progress in unraveling the genetic etiology of Parkinson disease in a genomic eraAline Verstraeten, Jessie Theuns, Christine Van Broeckhoven
Human Mutation|February 27, 2016
Marfan Syndrome and Related Disorders: 25 Years of Gene DiscoveryAline Verstraeten, Maaike Alaerts, Lut Van Laer, et al.
NPJ Genomic Medicine|November 22, 2022
SMAD6-deficiency in human genetic disordersIlse Luyckx, Aline Verstraeten, Marie-José Goumans, et al.
Trends in Molecular Medicine|June 9, 2020
Chondrodysplasias and Aneurysmal Thoracic Aortopathy: An Emerging Tale of Molecular IntersectionAline Verstraeten, Josephina Meester, Silke Peeters, et al.
Orphanet Journal of Rare Diseases|July 1, 2026
Preclinical modeling of Loeys-Dietz syndrome: insights into mechanisms and therapyAmira Bousbaa, Ivanna Fedoryshchenko, Ilse Luyckx, et al.
The Canadian Journal of Cardiology|November 26, 2015
Genetic Testing in Thoracic Aortic Disease--When, Why, and How?Sarah C Bowdin, Anne-Marie Laberge, Aline Verstraeten, et al.
Stem Cell Research|February 21, 2023
Generation of an induced pluripotent stem cell (iPSC) line of a Marfan syndrome patient with a pathogenic FBN1 c.5372G > A (p.Cys1791Tyr) variantSilke Peeters, Ivanna Fedoryshchenko, Laura Rabaut, et al.
Pageof 7

Showing results (1-10 of 64) with videos related to

Sort By:
Pageof 7
European Heart Journal|January 18, 2023
The emerging role of endothelial cells in the pathogenesis of thoracic aortic aneurysm and dissectionAline Verstraeten, Ivanna Fedoryshchenko, Bart Loeys
Nature Reviews. Cardiology|January 20, 2017
Aetiology and management of hereditary aortopathyAline Verstraeten, Ilse Luyckx, Bart Loeys
The Journal of Experimental Medicine|April 15, 2020
Hide and seek: Somatic SMAD3 mutations in melorheostosisJoe Davis Velchev, Aline Verstraeten, Bart Loeys
Trends in Genetics : TIG|February 24, 2015
Progress in unraveling the genetic etiology of Parkinson disease in a genomic eraAline Verstraeten, Jessie Theuns, Christine Van Broeckhoven
Human Mutation|February 27, 2016
Marfan Syndrome and Related Disorders: 25 Years of Gene DiscoveryAline Verstraeten, Maaike Alaerts, Lut Van Laer, et al.
NPJ Genomic Medicine|November 22, 2022
SMAD6-deficiency in human genetic disordersIlse Luyckx, Aline Verstraeten, Marie-José Goumans, et al.
Trends in Molecular Medicine|June 9, 2020
Chondrodysplasias and Aneurysmal Thoracic Aortopathy: An Emerging Tale of Molecular IntersectionAline Verstraeten, Josephina Meester, Silke Peeters, et al.
Orphanet Journal of Rare Diseases|July 1, 2026
Preclinical modeling of Loeys-Dietz syndrome: insights into mechanisms and therapyAmira Bousbaa, Ivanna Fedoryshchenko, Ilse Luyckx, et al.
The Canadian Journal of Cardiology|November 26, 2015
Genetic Testing in Thoracic Aortic Disease--When, Why, and How?Sarah C Bowdin, Anne-Marie Laberge, Aline Verstraeten, et al.
Stem Cell Research|February 21, 2023
Generation of an induced pluripotent stem cell (iPSC) line of a Marfan syndrome patient with a pathogenic FBN1 c.5372G > A (p.Cys1791Tyr) variantSilke Peeters, Ivanna Fedoryshchenko, Laura Rabaut, et al.
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