Detalhe da pesquisa
1.
Transcription co-factor LBH is necessary for the survival of cochlear hair cells.
J Cell Sci
; 134(7)2021 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33674448
2.
ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice.
Proc Natl Acad Sci U S A
; 113(21): 5993-8, 2016 May 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-27162350
3.
A dominant variant in the PDE1C gene is associated with nonsyndromic hearing loss.
Hum Genet
; 137(6-7): 437-446, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-29860631
4.
Indispensable Role of Ion Channels and Transporters in the Auditory System.
J Cell Physiol
; 232(4): 743-758, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-27704564
5.
Signaling in the Auditory System: Implications in Hair Cell Regeneration and Hearing Function.
J Cell Physiol
; 232(10): 2710-2721, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27869308
6.
Neurotransmitters: The Critical Modulators Regulating Gut-Brain Axis.
J Cell Physiol
; 232(9): 2359-2372, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-27512962
7.
A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation.
Hum Mol Genet
; 24(9): 2482-91, 2015 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25601850
8.
FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing.
Proc Natl Acad Sci U S A
; 111(27): 9864-8, 2014 Jul 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-24958875
9.
MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 Isoform.
Hum Mutat
; 37(5): 481-7, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26841241
10.
Tectorins crosslink type II collagen fibrils and connect the tectorial membrane to the spiral limbus.
J Struct Biol
; 194(2): 139-46, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26806019
11.
Molecular Structure and Regulation of P2X Receptors With a Special Emphasis on the Role of P2X2 in the Auditory System.
J Cell Physiol
; 231(8): 1656-70, 2016 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26627116
12.
Intricate Functions of Matrix Metalloproteinases in Physiological and Pathological Conditions.
J Cell Physiol
; 231(12): 2599-621, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27187048
13.
CRISPR: a versatile tool for both forward and reverse genetics research.
Hum Genet
; 135(9): 971-6, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27384229
14.
A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60.
Hum Genet
; 135(5): 513-524, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-27023905
15.
Mutation of the ATP-gated P2X(2) receptor leads to progressive hearing loss and increased susceptibility to noise.
Proc Natl Acad Sci U S A
; 110(6): 2228-33, 2013 Feb 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-23345450
16.
Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53.
Mol Genet Genomics
; 290(4): 1327-34, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25633957
17.
Myosin VIIa and sans localization at stereocilia upper tip-link density implicates these Usher syndrome proteins in mechanotransduction.
Proc Natl Acad Sci U S A
; 108(28): 11476-81, 2011 Jul 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-21709241
18.
Localization of PDZD7 to the stereocilia ankle-link associates this scaffolding protein with the Usher syndrome protein network.
J Neurosci
; 32(41): 14288-93, 2012 Oct 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-23055499
19.
Whirlin, a cytoskeletal scaffolding protein, stabilizes the paranodal region and axonal cytoskeleton in myelinated axons.
BMC Neurosci
; 14: 96, 2013 Sep 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-24011083
20.
Intermolecular autophosphorylation regulates myosin IIIa activity and localization in parallel actin bundles.
J Biol Chem
; 285(46): 35770-82, 2010 Nov 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-20826793