Detalhe da pesquisa
1.
Disease Model of GATA4 Mutation Reveals Transcription Factor Cooperativity in Human Cardiogenesis.
Cell;
167(7): 1734-1749.e22, 2016 Dec 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27984724
2.
Human disease modeling reveals integrated transcriptional and epigenetic mechanisms of NOTCH1 haploinsufficiency.
Cell;
160(6): 1072-86, 2015 Mar 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25768904
3.
Loss of PPARγ in endothelial cells leads to impaired angiogenesis.
J Cell Sci;
129(4): 693-705, 2016 Feb 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26743080
4.
Loss of bone morphogenetic protein receptor 2 is associated with abnormal DNA repair in pulmonary arterial hypertension.
Am J Respir Cell Mol Biol;
50(6): 1118-28, 2014 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24433082
5.
Autophagic protein LC3B confers resistance against hypoxia-induced pulmonary hypertension.
Am J Respir Crit Care Med;
183(5): 649-58, 2011 Mar 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20889906
6.
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.
Nat Genet;
49(6): 946-952, 2017 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28416818
7.
Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.
Nat Genet;
49(8): 1286, 2017 07 27.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28747752
8.
Disruption of PPARγ/ß-catenin-mediated regulation of apelin impairs BMP-induced mouse and human pulmonary arterial EC survival.
J Clin Invest;
121(9): 3735-46, 2011 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21821917