Detalhe da pesquisa
1.
Pervasive cortical and white matter anomalies in a mouse model for CHARGE syndrome.
J Anat
; 243(1): 51-65, 2023 07.
Artigo
Inglês
| MEDLINE | ID: mdl-36914558
2.
Distinct cerebellar foliation anomalies in a CHD7 haploinsufficient mouse model of CHARGE syndrome.
Am J Med Genet C Semin Med Genet
; 175(4)2017 12.
Artigo
Inglês
| MEDLINE | ID: mdl-29168327
3.
The neuroanatomy of autism - a developmental perspective.
J Anat
; 230(1): 4-15, 2017 01.
Artigo
Inglês
| MEDLINE | ID: mdl-27620360
4.
Organoid modeling of human fetal lung alveolar development reveals mechanisms of cell fate patterning and neonatal respiratory disease.
Cell Stem Cell
; 30(1): 20-37.e9, 2023 01 05.
Artigo
Inglês
| MEDLINE | ID: mdl-36493780
5.
Reduced chromatin accessibility correlates with resistance to Notch activation.
Nat Commun
; 13(1): 2210, 2022 04 25.
Artigo
Inglês
| MEDLINE | ID: mdl-35468895
6.
Cerebellar Vermis and Midbrain Hypoplasia Upon Conditional Deletion of Chd7 from the Embryonic Mid-Hindbrain Region.
Front Neuroanat
; 11: 86, 2017.
Artigo
Inglês
| MEDLINE | ID: mdl-29046629