1. Molecular mechanism of a new cardiac syndrome associated with a regulatory element deletion of chromosome 4q25. (25th November 2020) Authors: Baudic, M; Murata, H; Le Scouarnec, S; Foucal, A; Lindenbaum, P; Ishikawa, T; Si-Tayeb, K; Gaborit, N; Makita, N; Makiyama, T; Shimizu, W; Vieyres, C; Probst, V; Schott, J.J; Barc, J Journal: European heart journal Issue: Volume 41:(2020)Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Syndromic cardiac disorder is associated with a non-coding deletion that induces a 3D chromatin remodeling and PITX2 expression dysregulation. (3rd October 2022) Authors: Baudic, M; Murata, H; Bosada, F M; Souto Melo, U; Aizawa, T; Guedon, A; Lindenbaum, P; Gourraud, J B; Makita, N; Mundlos, S; Christoffels, V M; Makiyama, T; Probst, V; Schott, J J; Barc, J Journal: European heart journal Issue: Volume 43(2022)Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗