Detalhe da pesquisa
1.
Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss.
Hum Mol Genet
; 30(19): 1785-1796, 2021 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34059922
2.
Hearing loss, cleft palate, and congenital hip dysplasia in female carriers of an intragenic deletion of AMMECR1.
Am J Med Genet A
; 188(5): 1578-1582, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35084080
3.
A single-cell level comparison of human inner ear organoids with the human cochlea and vestibular organs.
Cell Rep
; 42(6): 112623, 2023 06 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-37289589
4.
Efficient Viral Transduction in Fetal and Adult Human Inner Ear Explants with AAV9-PHP.B Vectors.
Biomolecules
; 12(6)2022 06 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35740941
5.
Migration and fate of vestibular melanocytes during the development of the human inner ear.
Dev Neurobiol
; 80(11-12): 411-432, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33075185
6.
Low-dose oncolytic adenovirus therapy overcomes tumor-induced immune suppression and sensitizes intracranial gliomas to anti-PD-1 therapy.
Neurooncol Adv
; 2(1): vdaa011, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32642679
7.
A single-cell level comparison of human inner ear organoids with the human cochlea and vestibular organs.
Cell Rep
; 42(12): 113527, 2023 Dec 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38032795