168 related articles for article (PubMed ID: 18794526)
1. A catechol-O-methyltransferase that is essential for auditory function in mice and humans.
Du X; Schwander M; Moresco EM; Viviani P; Haller C; Hildebrand MS; Pak K; Tarantino L; Roberts A; Richardson H; Koob G; Najmabadi H; Ryan AF; Smith RJ; Müller U; Beutler B
Proc Natl Acad Sci U S A; 2008 Sep; 105(38):14609-14. PubMed ID: 18794526
[TBL] [Abstract][Full Text] [Related]
2. The murine catecholamine methyltransferase mTOMT is essential for mechanotransduction by cochlear hair cells.
Cunningham CL; Wu Z; Jafari A; Zhao B; Schrode K; Harkins-Perry S; Lauer A; Müller U
Elife; 2017 May; 6():. PubMed ID: 28504928
[TBL] [Abstract][Full Text] [Related]
3. A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function.
Schwander M; Sczaniecka A; Grillet N; Bailey JS; Avenarius M; Najmabadi H; Steffy BM; Federe GC; Lagler EA; Banan R; Hice R; Grabowski-Boase L; Keithley EM; Ryan AF; Housley GD; Wiltshire T; Smith RJ; Tarantino LM; Müller U
J Neurosci; 2007 Feb; 27(9):2163-75. PubMed ID: 17329413
[TBL] [Abstract][Full Text] [Related]
4. Elmod3 knockout leads to progressive hearing loss and abnormalities in cochlear hair cell stereocilia.
Li W; Feng Y; Chen A; Li T; Huang S; Liu J; Liu X; Liu Y; Gao J; Yan D; Sun J; Mei L; Liu X; Ling J
Hum Mol Genet; 2019 Dec; 28(24):4103-4112. PubMed ID: 31628468
[TBL] [Abstract][Full Text] [Related]
5. Null mutation of alpha1D Ca2+ channel gene results in deafness but no vestibular defect in mice.
Dou H; Vazquez AE; Namkung Y; Chu H; Cardell EL; Nie L; Parson S; Shin HS; Yamoah EN
J Assoc Res Otolaryngol; 2004 Jun; 5(2):215-26. PubMed ID: 15357422
[TBL] [Abstract][Full Text] [Related]
6. MPZL2, Encoding the Epithelial Junctional Protein Myelin Protein Zero-like 2, Is Essential for Hearing in Man and Mouse.
Wesdorp M; Murillo-Cuesta S; Peters T; Celaya AM; Oonk A; Schraders M; Oostrik J; Gomez-Rosas E; Beynon AJ; Hartel BP; Okkersen K; Koenen HJPM; Weeda J; Lelieveld S; Voermans NC; Joosten I; Hoyng CB; Lichtner P; Kunst HPM; Feenstra I; de Bruijn SE; ; Admiraal RJC; Yntema HG; van Wijk E; Del Castillo I; Serra P; Varela-Nieto I; Pennings RJE; Kremer H
Am J Hum Genet; 2018 Jul; 103(1):74-88. PubMed ID: 29961571
[TBL] [Abstract][Full Text] [Related]
7. Auditory Pathology in a Transgenic mtTFB1 Mouse Model of Mitochondrial Deafness.
McKay SE; Yan W; Nouws J; Thormann MJ; Raimundo N; Khan A; Santos-Sacchi J; Song L; Shadel GS
Am J Pathol; 2015 Dec; 185(12):3132-40. PubMed ID: 26552864
[TBL] [Abstract][Full Text] [Related]
8. A missense mutation in the conserved C2B domain of otoferlin causes deafness in a new mouse model of DFNB9.
Longo-Guess C; Gagnon LH; Bergstrom DE; Johnson KR
Hear Res; 2007 Dec; 234(1-2):21-8. PubMed ID: 17967520
[TBL] [Abstract][Full Text] [Related]
9. The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells.
Avraham KB; Hasson T; Steel KP; Kingsley DM; Russell LB; Mooseker MS; Copeland NG; Jenkins NA
Nat Genet; 1995 Dec; 11(4):369-75. PubMed ID: 7493015
[TBL] [Abstract][Full Text] [Related]
10. Quantitative measures reflect degeneration, but not regeneration, in the deafness mouse organ of Corti.
Faddis BT; Hughes RM; Miller JD
Hear Res; 1998 Jan; 115(1-2):6-12. PubMed ID: 9472731
[TBL] [Abstract][Full Text] [Related]
11. Neuroplastin Isoform Np55 Is Expressed in the Stereocilia of Outer Hair Cells and Required for Normal Outer Hair Cell Function.
Zeng WZ; Grillet N; Dewey JB; Trouillet A; Krey JF; Barr-Gillespie PG; Oghalai JS; Müller U
J Neurosci; 2016 Aug; 36(35):9201-16. PubMed ID: 27581460
[TBL] [Abstract][Full Text] [Related]
12. Deficiency of angulin-2/ILDR1, a tricellular tight junction-associated membrane protein, causes deafness with cochlear hair cell degeneration in mice.
Higashi T; Katsuno T; Kitajiri S; Furuse M
PLoS One; 2015; 10(3):e0120674. PubMed ID: 25822906
[TBL] [Abstract][Full Text] [Related]
13. The novel PMCA2 pump mutation Tommy impairs cytosolic calcium clearance in hair cells and links to deafness in mice.
Bortolozzi M; Brini M; Parkinson N; Crispino G; Scimemi P; De Siati RD; Di Leva F; Parker A; Ortolano S; Arslan E; Brown SD; Carafoli E; Mammano F
J Biol Chem; 2010 Nov; 285(48):37693-703. PubMed ID: 20826782
[TBL] [Abstract][Full Text] [Related]
14. Localization of efferent neurotransmitters in the inner ear of the homozygous Bronx waltzer mutant mouse.
Kong WJ; Scholtz AW; Hussl B; Kammen-Jolly K; Schrott-Fischer A
Hear Res; 2002 May; 167(1-2):136-55. PubMed ID: 12117537
[TBL] [Abstract][Full Text] [Related]
15. Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness.
Delmaghani S; Aghaie A; Michalski N; Bonnet C; Weil D; Petit C
Hum Mol Genet; 2012 Sep; 21(17):3835-44. PubMed ID: 22678063
[TBL] [Abstract][Full Text] [Related]
16. Progressive deafness and altered cochlear innervation in knock-out mice lacking prosaposin.
Akil O; Chang J; Hiel H; Kong JH; Yi E; Glowatzki E; Lustig LR
J Neurosci; 2006 Dec; 26(50):13076-88. PubMed ID: 17167097
[TBL] [Abstract][Full Text] [Related]
17. Characterization of a new allele of Ames waltzer generated by ENU mutagenesis.
Washington JL; Pitts D; Wright CG; Erway LC; Davis RR; Alagramam K
Hear Res; 2005 Apr; 202(1-2):161-9. PubMed ID: 15811708
[TBL] [Abstract][Full Text] [Related]
18. CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival.
Michel V; Booth KT; Patni P; Cortese M; Azaiez H; Bahloul A; Kahrizi K; Labbé M; Emptoz A; Lelli A; Dégardin J; Dupont T; Aghaie A; Oficjalska-Pham D; Picaud S; Najmabadi H; Smith RJ; Bowl MR; Brown SD; Avan P; Petit C; El-Amraoui A
EMBO Mol Med; 2017 Dec; 9(12):1711-1731. PubMed ID: 29084757
[TBL] [Abstract][Full Text] [Related]
19. Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31.
Mburu P; Mustapha M; Varela A; Weil D; El-Amraoui A; Holme RH; Rump A; Hardisty RE; Blanchard S; Coimbra RS; Perfettini I; Parkinson N; Mallon AM; Glenister P; Rogers MJ; Paige AJ; Moir L; Clay J; Rosenthal A; Liu XZ; Blanco G; Steel KP; Petit C; Brown SD
Nat Genet; 2003 Aug; 34(4):421-8. PubMed ID: 12833159
[TBL] [Abstract][Full Text] [Related]
20. Melody, an ENU mutation in Caspase 3, alters the catalytic cysteine residue and causes sensorineural hearing loss in mice.
Parker A; Hardisty-Hughes RE; Wisby L; Joyce S; Brown SD
Mamm Genome; 2010 Dec; 21(11-12):565-76. PubMed ID: 21116635
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
