Detalhe da pesquisa
1.
Glb1 knockout mouse model shares natural history with type II GM1 gangliosidosis patients.
Mol Genet Metab
; 138(2): 107508, 2023 02.
Artigo
Inglês
| MEDLINE | ID: mdl-36709532
2.
PUS7 deficiency in human patients causes profound neurodevelopmental phenotype by dysregulating protein translation.
Mol Genet Metab
; 135(3): 221-229, 2022 03.
Artigo
Inglês
| MEDLINE | ID: mdl-35144859
3.
Losses of sexual dichromatism involve rapid changes in female plumage colors to match males in New World blackbirds.
Evolution
; 78(1): 188-194, 2024 Jan 04.
Artigo
Inglês
| MEDLINE | ID: mdl-37943686