Aline S. Verstraeten

Antwerpen, VLG, Belgium

Last Updated: 09/26/2026

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Found 66 publications

Preclinical modeling of Loeys-Dietz syndrome: insights into mechanisms and therapy.

Preclinical modeling of Loeys-Dietz syndrome: insights into mechanisms and therapy.

Journal: Orphanet journal of rare diseases

Published: March 16, 2026

Genetic yield of targeted diagnostic screening in a large European cohort of 368 thoracic aortic dissection patients.

Genetic yield of targeted diagnostic screening in a large European cohort of 368 thoracic aortic dissection patients.

Journal: European journal of human genetics : EJHG

Published: December 10, 2025

Management of pregnancy in women with rare multisystemic vascular diseases: a qualitative survey analysis.

Management of pregnancy in women with rare multisystemic vascular diseases: a qualitative survey analysis.

Journal: Orphanet journal of rare diseases

Published: May 14, 2025

Sexual dimorphism in SMAD3 pathogenic variant-harbouring individuals.

Sexual dimorphism in SMAD3 pathogenic variant-harbouring individuals.

Journal: Journal of medical genetics

Published: July 03, 2024

Investigation of Strategies to Block Downstream Effectors of AT1R-Mediated Signalling to Prevent Aneurysm Formation in Marfan Syndrome.

Investigation of Strategies to Block Downstream Effectors of AT1R-Mediated Signalling to Prevent Aneurysm Formation in Marfan Syndrome.

Journal: International journal of molecular sciences

Published: March 15, 2024

Expanding the clinical spectrum of biglycan-related Meester-Loeys syndrome.

Expanding the clinical spectrum of biglycan-related Meester-Loeys syndrome.

Journal: NPJ genomic medicine

Published: December 01, 2023

Novel Association of the NOTCH Pathway Regulator MIB1 Gene With the Development of Bicuspid Aortic Valve.

Novel Association of the NOTCH Pathway Regulator MIB1 Gene With the Development of Bicuspid Aortic Valve.

Journal: JAMA cardiology

Published: July 05, 2023

Variable clinical expression of a Belgian TGFB3 founder variant suggests the presence of a genetic modifier.

Variable clinical expression of a Belgian TGFB3 founder variant suggests the presence of a genetic modifier.

Journal: Frontiers in genetics

Published: July 02, 2023

Generation of one induced pluripotent cell (iPSC) line (BBANTWi011-A) from a patient carrying an IPO8 bi-allelic loss-of-function mutation.

Generation of one induced pluripotent cell (iPSC) line (BBANTWi011-A) from a patient carrying an IPO8 bi-allelic loss-of-function mutation.

Journal: Stem cell research

Published: February 09, 2023

Generation of an induced pluripotent stem cell (iPSC) line of a Marfan syndrome patient with a pathogenic FBN1 c.5372G > A (p.Cys1791Tyr) variant.

Generation of an induced pluripotent stem cell (iPSC) line of a Marfan syndrome patient with a pathogenic FBN1 c.5372G > A (p.Cys1791Tyr) variant.

Journal: Stem cell research

Published: February 02, 2023

The emerging role of endothelial cells in the pathogenesis of thoracic aortic aneurysm and dissection.

The emerging role of endothelial cells in the pathogenesis of thoracic aortic aneurysm and dissection.

Journal: European heart journal

Published: January 18, 2023

IPSC reprogramming of two patients with spondyloepiphyseal dysplasia congenita (SEDC).

IPSC reprogramming of two patients with spondyloepiphyseal dysplasia congenita (SEDC).

Journal: Stem cell research

Published: January 13, 2023

Showing 1-12 of 66

Last Updated: 09/26/2026