Research Explorer

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Project

Study of the genetic basis and molecular pathogenesis of cardiovascular manifestations in heritable thoracic aortic aneurysms

Outputs & Impact

Publications & research data ( 2 )

Interpretation and classification of FBN1 variants associated with Marfan syndrome : consensus recommendations from the Clinical Genome Resource’s FBN1 variant curation expert panel

A. DrackleyC. SomervilleP. ArnaudL. M. BaudhuinN. HannaM. L. KlugeK. KotzerC. BoileauL. BronickiBert Callewaert et al.

A1 Journal Article in GENOME MEDICINE

Unraveling the role of TGFβ signaling in thoracic aortic aneurysm and dissection using Fbn1 mutant mouse models

Violette DeleeuwEric CarlsonMarjolijn RenardKeith D. ZientekPhillip A. WilmarthAshok P. ReddyElise C. ManaloSara F. TufaDouglas R. KeeneMargie Olbinado et al.

A1 Journal Article in MATRIX BIOLOGY

Activities ( 0 )

Results

Impact narratives ( 0 )

Patents ( 0 )