Detalhe da pesquisa
1.
Genetic modifiers modulate phenotypic expression of tafazzin deficiency in a mouse model of Barth syndrome.
Hum Mol Genet
; 32(12): 2055-2067, 2023 06 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36917259
2.
Tbx5 maintains atrial identity in post-natal cardiomyocytes by regulating an atrial-specific enhancer network.
Nat Cardiovasc Res
; 2(10): 881-898, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-38344303