Detalhe da pesquisa
1.
Mice Haploinsufficient for Ets1 and Fli1 Display Middle Ear Abnormalities and Model Aspects of Jacobsen Syndrome.
Am J Pathol
; 185(7): 1867-76, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26093983
2.
Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia.
Nat Genet
; 36(7): 725-31, 2004 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15184899
3.
An NZW-derived interval on chromosome 7 moderates sialadenitis, but not insulitis in congenic nonobese diabetic mice.
J Immunol
; 184(2): 859-68, 2010 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20007538
4.
ASK1 is a novel molecular target for preventing aminoglycoside-induced hair cell death.
J Mol Med (Berl)
; 100(5): 797-813, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35471608
5.
Intravenously delivered aminoglycoside antibiotics, tobramycin and amikacin, are not ototoxic in mice.
Hear Res
; 386: 107870, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31864009
6.
Analysis of prepulse inhibition in mouse lines overexpressing 22q11.2 orthologues.
Int J Neuropsychopharmacol
; 12(7): 983-9, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19519974
7.
Organotypic Culture of Neonatal Murine Inner Ear Explants.
Front Cell Neurosci
; 13: 170, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31130846
8.
Prevalence of Childhood Hearing Loss and Secular Trends: A Systematic Review and Meta-Analysis.
Acad Pediatr
; 19(5): 504-514, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30872125
9.
Effect of a pneumococcal whole cell vaccine on influenza A-induced pneumococcal otitis media in infant mice.
Vaccine
; 37(26): 3495-3504, 2019 06 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31103366
10.
An intronic mutation in Chd7 creates a cryptic splice site, causing aberrant splicing in a mouse model of CHARGE syndrome.
Sci Rep
; 8(1): 5482, 2018 04 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29615807
11.
Cross-sectional epidemiology of hearing loss in Australian children aged 11-12 years old and 25-year secular trends.
Arch Dis Child
; 103(6): 579-585, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29386180
12.
Correction to: ASK1 is a novel molecular target for preventing aminoglycosideinduced hair cell death.
J Mol Med (Berl)
; 100(5): 815, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35536324
13.
A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohort.
BMJ Paediatr Open
; 1(1): e000119, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29637142
14.
Data Resource Profile: The Victorian Childhood Hearing Impairment Longitudinal Databank (VicCHILD).
Int J Epidemiol
; 48(5): 1409-1410h, 2019 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31411681
15.
A new mouse model of Canavan leukodystrophy displays hearing impairment due to central nervous system dysmyelination.
Dis Model Mech
; 7(6): 649-57, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24682784
16.
CHD7 deficiency in "Looper", a new mouse model of CHARGE syndrome, results in ossicle malformation, otosclerosis and hearing impairment.
PLoS One
; 9(5): e97559, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24840056
17.
Description of a novel mutation leading to MYH9-related disease.
Thromb Res
; 122(6): 861-3, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18676005
18.
Two ENU-induced alleles of Atp2b2 cause deafness in mice.
PLoS One
; 8(6): e67479, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23826306
19.
Genetic Modifier Screens in Mice.
Curr Protoc Mouse Biol
; 2(1): 75-87, 2012 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26069006
20.
Vitamin D-deficient diet rescues hearing loss in Klotho mice.
Hear Res
; 275(1-2): 105-9, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21167925