Detalhe da pesquisa
1.
Sensory Neuron Diversity in the Inner Ear Is Shaped by Activity.
Cell
; 174(5): 1229-1246.e17, 2018 08 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-30078709
2.
Defects in the Alternative Splicing-Dependent Regulation of REST Cause Deafness.
Cell
; 174(3): 536-548.e21, 2018 07 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-29961578
3.
Deafness: from genetic architecture to gene therapy.
Nat Rev Genet
; 24(10): 665-686, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37173518
4.
Locus coeruleus activity improves cochlear implant performance.
Nature
; 613(7943): 317-323, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36544024
5.
A tribute to a remarkably sound solution.
Cell
; 154(6): 1175-7, 2013 Sep 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-24034237
6.
Neuronal Development of Hearing and Language: Cochlear Implants and Critical Periods.
Annu Rev Neurosci
; 42: 47-65, 2019 07 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30699049
7.
Mitochondrial stress engages E2F1 apoptotic signaling to cause deafness.
Cell
; 148(4): 716-26, 2012 Feb 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-22341444
8.
Expression of Atoh1, Gfi1, and Pou4f3 in the mature cochlea reprograms nonsensory cells into hair cells.
Proc Natl Acad Sci U S A
; 121(5): e2304680121, 2024 Jan 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38266052
9.
Disruption of Cdh23 exon 68 splicing leads to progressive hearing loss in mice by affecting tip-link stability.
Proc Natl Acad Sci U S A
; 121(10): e2309656121, 2024 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38408254
10.
Penetrance and expressivity of mitochondrial variants in a large clinically unselected population.
Hum Mol Genet
; 33(5): 465-474, 2024 Feb 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-37988592
11.
Preservation of developmental spontaneous activity enables early auditory system maturation in deaf mice.
PLoS Biol
; 21(6): e3002160, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37368868
12.
Restricted language access during childhood affects adult brain structure in selective language regions.
Proc Natl Acad Sci U S A
; 120(7): e2215423120, 2023 02 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-36745780
13.
Single-cell transcriptomic profiling of the mouse cochlea: An atlas for targeted therapies.
Proc Natl Acad Sci U S A
; 120(26): e2221744120, 2023 06 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-37339214
14.
Accurate phenotypic classification and exome sequencing allow identification of novel genes and variants associated with adult-onset hearing loss.
PLoS Genet
; 19(11): e1011058, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-38011198
15.
Gene burden analysis identifies genes associated with increased risk and severity of adult-onset hearing loss in a diverse hospital-based cohort.
PLoS Genet
; 19(1): e1010584, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36656851
16.
Age-Related Deficits in Binaural Hearing: Contribution of Peripheral and Central Effects.
J Neurosci
; 44(16)2024 Apr 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-38395618
17.
Neurotopographical Transformations: Dissecting Cortical Reconfigurations in Auditory Deprivation.
J Neurosci
; 44(13)2024 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38383498
18.
CLC Chloride Channels and Transporters: Structure, Function, Physiology, and Disease.
Physiol Rev
; 98(3): 1493-1590, 2018 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29845874
19.
A non-coding variant in 5' untranslated region drove up-regulation of pseudo-kinase EPHA10 and caused non-syndromic hearing loss in humans.
Hum Mol Genet
; 32(5): 720-731, 2023 02 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-36048850
20.
Mutations in human DNA methyltransferase DNMT1 induce specific genome-wide epigenomic and transcriptomic changes in neurodevelopment.
Hum Mol Genet
; 32(21): 3105-3120, 2023 10 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-37584462