Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Julia C. Wilmanns"'
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:
Nadia Rosenthal, Milena B. Furtado, Vivek M. Philip, Stuart K. Archer, Jan M. Schilling, Anjana Chandran, Raghav Pandey, Hemal H. Patel, Julia C. Wilmanns, Gael Cagnone, Qizhu Wu, James T. Pearson, Joerg Heineke, Olivia J Hon, Preeti Bais, Mauro W. Costa, Heidi Kocalis, Mirana Ramialison, Elvira Forte, David Coleman
Publikováno v:
Molecular Metabolism, Vol 20, Iss, Pp 102-114 (2019)
Molecular Metabolism
Molecular Metabolism
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 ACH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71a383ac285cbbfbdd1f63a52c6c8197
http://www.sciencedirect.com/science/article/pii/S2212877818308366
http://www.sciencedirect.com/science/article/pii/S2212877818308366
Autor:
Julia C. Wilmanns, Mauro W. Costa, Nadia Rosenthal, Milena B. Furtado, Olivia J Hon, Raghav Pandey
Publikováno v:
Circulation Research. 125
Objective: Congenital heart disease (CHD) is the most frequent birth defect worldwide. Improved surgical and treatment interventions have led to a significant increase in the number of adult patients with CHD, now referred to as ACHD. However the mec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae23df7cd9d19c95b719dd47916eb96a
https://doi.org/10.1161/res.125.suppl_1.275
https://doi.org/10.1161/res.125.suppl_1.275
Autor:
Christine Biben, James T. Pearson, Mary A Tonta, Mirana Ramialison, Julia C. Wilmanns, Michael P. Eichenlaub, Mauro W. Costa, Helena C. Parkington, Romaric Bouveret, Milena B. Furtado, Harold A. Coleman, Anjana Chandran, Richard P. Harvey, Silke Berger, Nadia Rosenthal, Reena Singh
Publikováno v:
Differentiation. 91:29-41
Nkx2-5 is one of the master regulators of cardiac development, homeostasis and disease. This transcription factor has been previously associated with a suite of cardiac congenital malformations and impairment of electrical activity. When disease caus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc10403a4947bc4cd955632809be6233
https://doi.org/10.1016/j.diff.2015.12.003
https://doi.org/10.1016/j.diff.2015.12.003
Autor:
Mirana Ramialison, James T. Pearson, Gael Cagnone, Qizhu Wu, Jan M. Schilling, Preeti Bais, Raghav Pandey, Olivia J Hon, Milena B. Furtado, Hemal H. Patel, Vivek M. Philip, Heidi Kocalis, Stuart K. Archer, Nadia Rosenthal, Julia C. Wilmanns, Anjana Chandran, Mauro W. Costa, Joerg Heineke
Congenital heart disease (CHD) is the most frequent birth defect worldwide and the number of adult patients with CHD, now referred to as ACHD, is increasing. However the mechanisms whereby ACHD predisposes patients to heart dysfunction are still uncl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b2a37fc93d8b329144d3c284ba3a24c
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