Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Olivia Hon"'
Autor:
Julia C. Wilmanns, Raghav Pandey, Olivia Hon, Anjana Chandran, Jan M. Schilling, Elvira Forte, Qizhu Wu, Gael Cagnone, Preeti Bais, Vivek Philip, David Coleman, Heidi Kocalis, Stuart K. Archer, James T. Pearson, Mirana Ramialison, Joerg Heineke, Hemal H. Patel, Nadia A. Rosenthal, Milena B. Furtado, Mauro W. Costa
Publikováno v:
Molecular Metabolism, Vol 20, Iss , Pp 102-114 (2019)
Objective: Congenital heart disease (CHD) is the most frequent birth defect worldwide. The number of adult patients with CHD, now referred to as ACHD, is increasing with improved surgical and treatment interventions. However the mechanisms whereby AC
Externí odkaz:
https://doaj.org/article/54e4286b7710480bb545986201e5fddc
Autor:
Elvira Forte, Daniel A. Skelly, Mandy Chen, Sandra Daigle, Kaesi A. Morelli, Olivia Hon, Vivek M. Philip, Mauro W. Costa, Nadia A. Rosenthal, Milena B. Furtado
Publikováno v:
Cell Reports, Vol 30, Iss 9, Pp 3149-3163.e6 (2020)
Summary: Cardiac ischemia leads to the loss of myocardial tissue and the activation of a repair process that culminates in the formation of a scar whose structural characteristics dictate propensity to favorable healing or detrimental cardiac wall ru
Externí odkaz:
https://doaj.org/article/4c04a1b1b8cc4f488dda97c0c6b71aa6
Autor:
Meghan Flanigan, Olivia Hon, Shannon D’Ambrosio, Kristen Boyt, Leslie Hassaenein, Megan Castle, Harold Haun, Melanie Pina, Thomas L. Kash
Publikováno v:
Alcohol. 109:96
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1efd826d01fbc652099c6e804f736c9
https://doi.org/10.1016/j.alcohol.2023.03.115
https://doi.org/10.1016/j.alcohol.2023.03.115
Autor:
Qi-Zhu Wu, Diane Fatkin, Nicolas Plachta, Anjana Chandran, Stephanie E. Simonds, Milena B. Furtado, Nadia Rosenthal, James T. Pearson, Christine Biben, David Willians, Taylor J. Willow, Gurpreet Kaur, Joelle Perera, Hieu T. Nim, Richard P. Harvey, Julia C. Wilmanns, Ekaterina Salimova, James M. Denegre, Olivia Hon, David M. Kaye, Mirana Ramialison, Stephen A. Murray, Mauro W. Costa, Michael A. Cowley
Mutations in the Nkx2-5 gene are a main cause of congenital heart disease. Several studies have addressed the phenotypic consequences of disrupting the Nkx2-5 gene locus, although animal models to date failed to recapitulate the full spectrum of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f696b31663b1143e8fa0f2aa2167515e
http://hdl.handle.net/10044/1/56521
http://hdl.handle.net/10044/1/56521
