Items where Author is "Costa, Mauro W"

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | No Grouping
Jump to: Article
Number of items: 6.


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)

This list was generated on Sun Dec 8 11:04:20 2019 AEDT.