Items where Author is "Costa, Mauro W"

Article

Choquet, Caroline and Nguyen, Thi Hong Minh and Sicard, Pierre and Buttigieg, Emeline and Tran, Thi Thom and Kober, Frank and Varlet, Isabelle and Sturny, Rachel and Costa, Mauro W and Harvey, Richard P and Nguyen, Catherine and Rihet, Pascal and Richard, Sylvain and Bernard, Monique and Kelly, Robert G. and Lalevée, Nathalie and Miquerol, Lucile (2018) Deletion of Nkx2-5 in trabecular myocardium reveals the developmental origins of pathological heterogeneity associated with ventricular non-compaction cardiomyopathy. PLoS Genetics, 14 (7). pp. e1007502. ISSN 1553-7404 (Gold OA)

Anderson, David J and Kaplan, David I and Bell, Katrina M and Koutsis, Katerina and Haynes, John M and Mills, Richard J and Phelan, Dean G and Qian, Elizabeth L and Leitoguinho, Ana Rita and Arasaratnam, Deevina and Labonne, Tanya and Ng, Elizabeth S and Davis, Richard P and Casini, Simona and Passier, Robert and Hudson, James E and Porrello, Enzo R and Costa, Mauro W and Rafii, Arash and Curl, Clare L and Delbridge, Lea M and Harvey, Richard P and Oshlack, Alicia and Cheung, Michael M and Mummery, Christine L and Petrou, Stephen and Elefanty, Andrew G and Stanley, Edouard G and Elliott, David A (2018) NKX2-5 regulates human cardiomyogenesis via a HEY2 dependent transcriptional network. Nature Communications, 9 (1). p. 1373. ISSN 2041-1723 (PMC OA)

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)

Furtado, Milena B and Wilmanns, Julia C and Chandran, Anjana and Tonta, Mary and Biben, Christine and Eichenlaub, Michael and Coleman, Harold A and Berger, Silke and Bouveret, Romaric and Singh, Reena and Harvey, Richard P and Ramialison, Mirana and Pearson, James T and Parkington, Helena C and Rosenthal, Nadia A and Costa, Mauro W (2016) A novel conditional mouse model for Nkx2-5 reveals transcriptional regulation of cardiac ion channels. Differentiation, 91. pp.29-41. ISSN 1432-0436 (PP OA)

Furtado, Milena B and Costa, Mauro W and Pranoto, Edward A and Salimova, Ekaterina and Pinto, Alexander R and Lam, Nicholas T and Park, Anthony and Snider, Paige and Chandran, Anjana and Harvey, Richard P and Boyd, Richard and Conway, Simon J and Pearson, James and Kaye, David M and Rosenthal, Nadia A (2014) Cardiogenic genes expressed in cardiac fibroblasts contribute to heart development and repair. Circulation Research, 114 (9). pp.1422-34. ISSN 1524-4571 (PMC OA)

Costa, Mauro W and Guo, Guanglan and Wolstein, Orit and Vale, Molly and Castro, Maria L and Wang, Libin and Otway, Robyn and Riek, Peter and Cochrane, Natalie and Furtado, Milena B and Semsarian, Christopher and Weintraub, Robert G and Yeoh, Thomas and Hayward, Christopher S and Keogh, Anne and Macdonald, Peter S and Feneley, Michael P and Graham, Robert M and Seidman, Jonathan G and Seidman, Christine E and Rosenthal, Nadia and Fatkin, Diane and Harvey, Richard P (2013) Functional characterization of a novel mutation in NKX2-5 associated with congenital heart disease and adult-onset cardiomyopathy. Circulation: Cardiovascular Genetics, 6 (3). pp.238-47. ISSN 1942-3268 (PMC OA)