Detalhe da pesquisa
1.
Intestinal brush border assembly driven by protocadherin-based intermicrovillar adhesion.
Cell
; 157(2): 433-446, 2014 Apr 10.
Artigo
Inglês
| MEDLINE | ID: mdl-24725409
2.
A Novel missense mutation of COL2A1 gene in a large family with stickler syndrome type I.
J Cell Mol Med
; 26(5): 1530-1539, 2022 03.
Artigo
Inglês
| MEDLINE | ID: mdl-35064646
3.
Phenotypic differences in the inner ears of CBA/CaJ and C57BL/6J mice carrying missense and single base pair deletion mutations in the Cdh23 gene.
J Neurosci Res
; 99(10): 2743-2758, 2021 10.
Artigo
Inglês
| MEDLINE | ID: mdl-34133797
4.
Biomechanical Analysis of Angular Motion in Association with Bilateral Semicircular Canal Function.
Biophys J
; 118(3): 729-741, 2020 02 04.
Artigo
Inglês
| MEDLINE | ID: mdl-31928764
5.
A systems genetics approach to revealing the Pdgfb molecular network of the retina.
Mol Vis
; 26: 459-471, 2020.
Artigo
Inglês
| MEDLINE | ID: mdl-32587457
6.
An Age-Related Hearing Protection Locus on Chromosome 16 of BXD Strain Mice.
Neural Plast
; 2020: 8889264, 2020.
Artigo
Inglês
| MEDLINE | ID: mdl-32587610
7.
Treatment of ear and bone disease in the Phex mouse mutant with dietary supplementation.
Am J Otolaryngol
; 38(1): 44-51, 2017.
Artigo
Inglês
| MEDLINE | ID: mdl-27733274
8.
The ROS derived mitochondrial respirstion not from NADPH oxidase plays key role in Celastrol against angiotensin II-mediated HepG2 cell proliferation.
Apoptosis
; 21(11): 1315-1326, 2016 11.
Artigo
Inglês
| MEDLINE | ID: mdl-27658784
9.
Digenic inheritance of deafness caused by 8J allele of myosin-VIIA and mutations in other Usher I genes.
Hum Mol Genet
; 21(11): 2588-98, 2012 Jun 01.
Artigo
Inglês
| MEDLINE | ID: mdl-22381527
10.
Pathological features in the LmnaDhe/+ mutant mouse provide a novel model of human otitis media and laminopathies.
Am J Pathol
; 181(3): 761-74, 2012 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-22819531
11.
Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss.
Nat Genet
; 35(1): 21-3, 2003 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-12910270
12.
Microtubule-associated protein 1A is a modifier of tubby hearing (moth1).
Nat Genet
; 30(4): 401-5, 2002 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-11925566
13.
Endolymphatic Hydrop Phenotype in Familial Norrie Disease Caused by Large Fragment Deletion of NDP.
Front Aging Neurosci
; 14: 771328, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35517050
14.
gom1 Mutant Mice as a Model of Otitis Media.
J Assoc Res Otolaryngol
; 23(2): 213-223, 2022 04.
Artigo
Inglês
| MEDLINE | ID: mdl-35118601
15.
Hippocampal Transcriptome-Wide Association Study Reveals Correlations Between Impaired Glutamatergic Synapse Pathway and Age-Related Hearing Loss in BXD-Recombinant Inbred Mice.
Front Neurosci
; 15: 745668, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-34867157
16.
Autophagy Contributes to the Rapamycin-Induced Improvement of Otitis Media.
Front Cell Neurosci
; 15: 753369, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-35153674
17.
Autophagy impairment as a key feature for acetaminophen-induced ototoxicity.
Cell Death Dis
; 12(1): 3, 2021 01 04.
Artigo
Inglês
| MEDLINE | ID: mdl-33414397
18.
Screening mutations of OTOF gene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathy.
BMC Med Genet
; 11: 79, 2010 May 26.
Artigo
Inglês
| MEDLINE | ID: mdl-20504331
19.
RNA-seq analysis of potential lncRNAs for age-related hearing loss in a mouse model.
Aging (Albany NY)
; 12(8): 7491-7510, 2020 04 26.
Artigo
Inglês
| MEDLINE | ID: mdl-32335544
20.
The podosomal-adaptor protein SH3PXD2B is essential for normal postnatal development.
Mamm Genome
; 20(8): 462-75, 2009 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-19669234