Detalhe da pesquisa
1.
ß1-integrin is a cell-autonomous factor mediating the Numb pathway for cardiac progenitor maintenance.
Biochem Biophys Res Commun
; 500(2): 256-260, 2018 06 02.
Artigo
Inglês
| MEDLINE | ID: mdl-29653101
2.
Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies.
Hum Mol Genet
; 24(14): 3994-4005, 2015 Jul 15.
Artigo
Inglês
| MEDLINE | ID: mdl-25877302
3.
Cilia and Ciliopathies in Congenital Heart Disease.
Cold Spring Harb Perspect Biol
; 9(8)2017 Aug 01.
Artigo
Inglês
| MEDLINE | ID: mdl-28159874
4.
Prickle1 mutation causes planar cell polarity and directional cell migration defects associated with cardiac outflow tract anomalies and other structural birth defects.
Biol Open
; 5(3): 323-35, 2016 Feb 16.
Artigo
Inglês
| MEDLINE | ID: mdl-26883626