Detalhe da pesquisa
1.
BBSome function is required for both the morphogenesis and maintenance of the photoreceptor outer segment.
PLoS Genet
; 13(10): e1007057, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29049287
2.
Mutations in C8ORF37 cause Bardet Biedl syndrome (BBS21).
Hum Mol Genet
; 25(11): 2283-2294, 2016 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27008867
3.
The absence of BBSome function decreases synaptogenesis and causes ectopic synapse formation in the retina.
Sci Rep
; 10(1): 8321, 2020 05 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-32433491
4.
Absence of BBSome function leads to astrocyte reactivity in the brain.
Mol Brain
; 12(1): 48, 2019 05 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31072410
5.
Keeping an Eye on Bardet-Biedl Syndrome: A Comprehensive Review of the Role of Bardet-Biedl Syndrome Genes in the Eye.
Med Res Arch
; 5(9)2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-29457131