Altered TGFβ signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency
Marjolijn Renard(Ghent University Hospital), Bart Loeys(Radboud University Nijmegen)
Cited by 151
Related Papers
A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2
|Nature Genetics|2005|1.8k
Mutations in a TGF-β Ligand, TGFB3, Cause Syndromic Aortic Aneurysms and Dissections
|Journal of the American College of Cardiology|2015|292
Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAAD
|International Journal of Cardiology|2011|170
Morpho-functional comparison of differentiation protocols to create iPSC-derived cardiomyocytes
|Biology Open|2022|8
Expanding the clinical spectrum of biglycan-related Meester-Loeys syndrome
|npj Genomic Medicine|2024|4