Detalhe da pesquisa
1.
Reversal of an existing hearing loss by gene activation in Spns2 mutant mice.
Proc Natl Acad Sci U S A
; 120(34): e2307355120, 2023 08 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-37552762
2.
Mouse screen reveals multiple new genes underlying mouse and human hearing loss.
PLoS Biol
; 17(4): e3000194, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30973865
3.
ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cells.
Hum Mol Genet
; 24(3): 609-24, 2015 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25217574
4.
Insights into the pathophysiology of DFNA44 hearing loss associated with CCDC50 frameshift variants.
Dis Model Mech
; 16(8)2023 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37165931
5.
The Effect of a Pex3 Mutation on Hearing and Lipid Content of the Inner Ear.
Cells
; 11(20)2022 10 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36291074
6.
Synaptojanin2 Mutation Causes Progressive High-frequency Hearing Loss in Mice.
Front Cell Neurosci
; 14: 561857, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33100973
7.
Reversible Notch1 acetylation tunes proliferative signalling in cardiomyocytes.
Cardiovasc Res
; 114(1): 103-122, 2018 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29186476