Detalhe da pesquisa
1.
SMARCA4 mutation causes human otosclerosis and a similar phenotype in mice.
J Med Genet
; 61(2): 117-124, 2024 Jan 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-37399313
2.
Shared and organ-specific gene-expression programs during the development of the cochlea and the superior olivary complex.
RNA Biol
; 20(1): 629-640, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37602850
3.
The noncoding genome and hearing loss.
Hum Genet
; 141(3-4): 323-333, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-34491412
4.
The long and short: Non-coding RNAs in the mammalian inner ear.
Hear Res
; 428: 108666, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36566643
5.
High-throughput analysis of the transcriptional patterns of sexual genes in malaria.
Parasit Vectors
; 16(1): 14, 2023 Jan 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36639683
6.
Repair of noise-induced damage to stereocilia F-actin cores is facilitated by XIRP2 and its novel mechanosensor domain.
Elife
; 122023 Jun 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37294664
7.
DNA methylation dynamics during embryonic development and postnatal maturation of the mouse auditory sensory epithelium.
Sci Rep
; 8(1): 17348, 2018 11 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-30478432