Molecular Signature of CAID Syndrome: Noncanonical Roles of SGO1 in Regulation of TGF-β Signaling and EpigenomicsSummary

Autor: Jessica Piché, Natacha Gosset, Lisa-Marie Legault, Alain Pacis, Andrea Oneglia, Maxime Caron, Philippe Chetaille, Luis Barreiro, Donghai Liu, Xioyan Qi, Stanley Nattel, Séverine Leclerc, Mélanie Breton-Larrivée, Serge McGraw, Gregor Andelfinger, Jeroen Bakkers, Bart Loeys, Michel Pucéat

Publikováno v: Cellular and Molecular Gastroenterology and Hepatology, Vol 7, Iss 2, Pp 411-431 (2019)
Cellular and Molecular Gastroenterology and Hepatology
CELLULAR AND MOLECULAR GASTROENTEROLOGY AND HEPATOLOGY, 7(2), 411-431
CELLULAR AND MOLECULAR GASTROENTEROLOGY AND HEPATOLOGY
CELLULAR AND MOLECULAR GASTROENTEROLOGY AND HEPATOLOGY, 2019, 7 (2), pp.411-431. ⟨10.1016/j.jcmgh.2018.10.011⟩
CMGH Cellular and Molecular Gastroenterology and Hepatology

Background & Aims A generalized human pacemaking syndrome, chronic atrial and intestinal dysrhythmia (CAID) (OMIM 616201), is caused by a homozygous SGO1 mutation (K23E), leading to chronic intestinal pseudo-obstruction and arrhythmias. Because CAID

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c86c6072048d78e405868a6d89bbe835
http://www.sciencedirect.com/science/article/pii/S2352345X18301577