Items where Author is "Plachta, Nicolas"

Article

Furtado, Milena B and Wilmanns, Julia C and Chandran, Anjana and Perera, Joelle and Hon, Olivia and Biben, Christine and Willow, Taylor J and Nim, Hieu T and Kaur, Gurpreet and Simonds, Stephanie and Wu, Qizhu and Willians, David and Salimova, Ekaterina and Plachta, Nicolas and Denegre, James M and Murray, Stephen A and Fatkin, Diane and Cowley, Michael and Pearson, James T and Kaye, David and Ramialison, Mirana and Harvey, Richard P and Rosenthal, Nadia A and Costa, Mauro W (2017) Point mutations in murine Nkx2-5 phenocopy human congenital heart disease and induce pathogenic Wnt signaling. JCI Insight, 2 (6). pp. e88271. ISSN 2379-3708 (PMC OA)

Bouveret, Romaric and Waardenberg, Ashley J and Schonrock, Nicole and Ramialison, Mirana and Doan, Tram and de Jong, Danielle and Bondue, Antoine and Kaur, Gurpreet and Mohamed, Stephanie and Fonoudi, Hananeh and Chen, Chiann-Mun and Wouters, Merridee A and Bhattacharya, Shoumo and Plachta, Nicolas and Dunwoodie, Sally L and Chapman, Gavin and Blanpain, Cédric and Harvey, Richard P (2015) NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets. eLife, 4. ISSN 2050-084X (OA)