Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Adrianna Matos-Nieves"'
Autor:
Adrianna Matos-Nieves, Sathiyanarayanan Manivannan, Uddalak Majumdar, Kim L. McBride, Peter White, Vidu Garg
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2021)
Congenital heart disease (CHD) is the most common type of birth defect, affecting ~1% of all live births. Malformations of the cardiac outflow tract (OFT) account for ~30% of all CHD and include a range of CHDs from bicuspid aortic valve (BAV) to tet
Externí odkaz:
https://doaj.org/article/45e92b2848d14e02b97190d9d9701f15
Autor:
Stephanie LaHaye, Uddalak Majumdar, Jun Yasuhara, Sara N. Koenig, Adrianna Matos-Nieves, Rahul Kumar, Vidu Garg
Publikováno v:
Disease Models & Mechanisms, Vol 12, Iss 6 (2019)
Congenital heart defects affect ∼2% of live births and often involve malformations of the semilunar (aortic and pulmonic) valves. We previously reported a highly penetrant GATA4 p.Gly296Ser mutation in familial, congenital atrial septal defects and
Externí odkaz:
https://doaj.org/article/cbba6851e3e94a3985c35f1b29905da0
Autor:
Jeffrey S. Bennett, David M. Gordon, Uddalak Majumdar, Patrick J. Lawrence, Adrianna Matos-Nieves, Katherine Myers, Anna N. Kamp, Julie C. Leonard, Kim L. McBride, Peter White, Vidu Garg
Publikováno v:
Heart Rhythm
BACKGROUND: Variation in Lamin A/C results in a spectrum of clinical disease, including arrhythmias and cardiomyopathy. Benign variation is rare, and classification of LMNA missense variants via in silico prediction tools results in a high rate of va
Autor:
Vanessa Hertig, Adrianna Matos‐Nieves, Vidu Garg, Louis Villeneuve, Maya Mamarbachi, Laurie Caland, Angelino Calderone
Publikováno v:
Journal of Cellular Physiology. 234
Publikováno v:
Circulation research. 124(4)
RATIONALE: Familial recurrence studies provide strong evidence for a genetic component to the predisposition to sporadic, non-syndromic Tetralogy of Fallot (TOF), the most common cyanotic congenital heart disease (CHD) phenotype. Rare genetic variant
Autor:
Rahul Kumar, Sara N. Koenig, Jun Yasuhara, Stephanie LaHaye, Vidu Garg, Uddalak Majumdar, Adrianna Matos-Nieves
Publikováno v:
Disease Models & Mechanisms, Vol 12, Iss 6 (2019)
Congenital heart defects affect ∼2% of live births and often involve malformations of the semilunar (aortic and pulmonic) valves. We previously reported a highly penetrant GATA4 p.Gly296Ser mutation in familial, congenital atrial septal defects and
Autor:
Stephanie, LaHaye, Uddalak, Majumdar, Jun, Yasuhara, Sara N, Koenig, Adrianna, Matos-Nieves, Rahul, Kumar, Vidu, Garg
Publikováno v:
Disease Models & Mechanisms
Congenital heart defects affect ∼2% of live births and often involve malformations of the semilunar (aortic and pulmonic) valves. We previously reported a highly penetrant GATA4 p.Gly296Ser mutation in familial, congenital atrial septal defects and
Autor:
Vanessa Hertig, Adrianna Matos-Nieves, Vidu Garg, Louis Villeneuve, Maya Mamarbachi, Laurie Caland, Angelino Calderone
Publikováno v:
Journal of Cellular Physiology. 233:i-i