Silke Peeters

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 5

Top Topics

Vascular Smooth Muscle Cells

Aortic Aneurysm

Coronary Artery

Top Venues

International journal of molecular sciences

Journal of medical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Irene Valdivia Callejon, Lucia Buccioli, Jarl Bastianen, Jolien Schippers, Aline Verstraeten, Ilse Luyckx, Silke Peeters, Alexander H J Danser, Roland R J Van Kimmenade, Josephina A N Meester, Bart L Loeys
Investigation of Strategies to Block Downstream Effectors of AT1R-Mediated Signalling to Prevent Aneurysm Formation in Marfan Syndrome. International journal of molecular sciences 25 (9) (2024)
Irene Valdivia Callejon, Lucia Buccioli, Jarl Bastianen, Jolien Schippers, Aline Verstraeten, Ilse Luyckx, Silke Peeters, Alexander H J Danser, Roland R J Van Kimmenade, Josephina A N Meester, Bart L Loeys
Investigation of Strategies to Block Downstream Effectors of AT1R-Mediated Signalling to Prevent Aneurysm Formation in Marfan Syndrome. International journal of molecular sciences 25 (9) (2024)
Irene Valdivia Callejon, Lucia Buccioli, Jarl Bastianen, Jolien Schippers, Aline Verstraeten, Ilse Luyckx, Silke Peeters, Alexander H J Danser, Roland R J Van Kimmenade, Josephina A N Meester, Bart L Loeys
Investigation of Strategies to Block Downstream Effectors of AT1R-Mediated Signalling to Prevent Aneurysm Formation in Marfan Syndrome. International journal of molecular sciences 25 (9) (2024)
Silke Peeters, Pauline De Kinderen, Josephina A N Meester, Aline Verstraeten, Bart L Loeys
The fibrillinopathies: New insights with focus on the paradigm of opposing phenotypes for both FBN1 and FBN2. Human mutation 43 (7) (2022)
Silke Peeters, Arne Decramer, Stuart Alan Cain, Peter Houpt, Frederik Verstreken, Jan Noyez, Christophe Hermans, Werner Jacobs, Martin Lammens, Erik Fransen, Ajay Anand Kumar, Geert Vandeweyer, Bart Loeys, Wim Van Hul, Clair Baldock, Eveline Boudin, Geert Mortier
Delineation of a new fibrillin-2-opathy with evidence for a role of FBN2 in the pathogenesis of carpal tunnel syndrome. Journal of medical genetics 58 (11) (2020)