381 related articles for article (PubMed ID: 10760300)
1. KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway.
Kharkovets T; Hardelin JP; Safieddine S; Schweizer M; El-Amraoui A; Petit C; Jentsch TJ
Proc Natl Acad Sci U S A; 2000 Apr; 97(8):4333-8. PubMed ID: 10760300
[TBL] [Abstract][Full Text] [Related]
2. KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness.
Kubisch C; Schroeder BC; Friedrich T; Lütjohann B; El-Amraoui A; Marlin S; Petit C; Jentsch TJ
Cell; 1999 Feb; 96(3):437-46. PubMed ID: 10025409
[TBL] [Abstract][Full Text] [Related]
3. Vestibular role of KCNQ4 and KCNQ5 K+ channels revealed by mouse models.
Spitzmaul G; Tolosa L; Winkelman BH; Heidenreich M; Frens MA; Chabbert C; de Zeeuw CI; Jentsch TJ
J Biol Chem; 2013 Mar; 288(13):9334-44. PubMed ID: 23408425
[TBL] [Abstract][Full Text] [Related]
4. Longitudinal gradients of KCNQ4 expression in spiral ganglion and cochlear hair cells correlate with progressive hearing loss in DFNA2.
Beisel KW; Nelson NC; Delimont DC; Fritzsch B
Brain Res Mol Brain Res; 2000 Oct; 82(1-2):137-49. PubMed ID: 11042367
[TBL] [Abstract][Full Text] [Related]
5. Resting potential and submembrane calcium concentration of inner hair cells in the isolated mouse cochlea are set by KCNQ-type potassium channels.
Oliver D; Knipper M; Derst C; Fakler B
J Neurosci; 2003 Mar; 23(6):2141-9. PubMed ID: 12657673
[TBL] [Abstract][Full Text] [Related]
6. Mice with altered KCNQ4 K+ channels implicate sensory outer hair cells in human progressive deafness.
Kharkovets T; Dedek K; Maier H; Schweizer M; Khimich D; Nouvian R; Vardanyan V; Leuwer R; Moser T; Jentsch TJ
EMBO J; 2006 Feb; 25(3):642-52. PubMed ID: 16437162
[TBL] [Abstract][Full Text] [Related]
7. Inner Hair Cell and Neuron Degeneration Contribute to Hearing Loss in a DFNA2-Like Mouse Model.
Carignano C; Barila EP; Rías EI; Dionisio L; Aztiria E; Spitzmaul G
Neuroscience; 2019 Jul; 410():202-216. PubMed ID: 31102762
[TBL] [Abstract][Full Text] [Related]
8. Impaired surface expression and conductance of the KCNQ4 channel lead to sensorineural hearing loss.
Gao Y; Yechikov S; Vázquez AE; Chen D; Nie L
J Cell Mol Med; 2013 Jul; 17(7):889-900. PubMed ID: 23750663
[TBL] [Abstract][Full Text] [Related]
9. Dominant-negative inhibition of M-like potassium conductances in hair cells of the mouse inner ear.
Holt JR; Stauffer EA; Abraham D; Géléoc GS
J Neurosci; 2007 Aug; 27(33):8940-51. PubMed ID: 17699675
[TBL] [Abstract][Full Text] [Related]
10. Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region.
Van Hauwe P; Coucke PJ; Ensink RJ; Huygen P; Cremers CW; Van Camp G
Am J Med Genet; 2000 Jul; 93(3):184-7. PubMed ID: 10925378
[TBL] [Abstract][Full Text] [Related]
11. Restoration of ion channel function in deafness-causing KCNQ4 mutants by synthetic channel openers.
Leitner MG; Feuer A; Ebers O; Schreiber DN; Halaszovich CR; Oliver D
Br J Pharmacol; 2012 Apr; 165(7):2244-59. PubMed ID: 21951272
[TBL] [Abstract][Full Text] [Related]
12. Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.
Coucke PJ; Van Hauwe P; Kelley PM; Kunst H; Schatteman I; Van Velzen D; Meyers J; Ensink RJ; Verstreken M; Declau F; Marres H; Kastury K; Bhasin S; McGuirt WT; Smith RJ; Cremers CW; Van de Heyning P; Willems PJ; Smith SD; Van Camp G
Hum Mol Genet; 1999 Jul; 8(7):1321-8. PubMed ID: 10369879
[TBL] [Abstract][Full Text] [Related]
13. Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss.
Talebizadeh Z; Kelley PM; Askew JW; Beisel KW; Smith SD
Hum Mutat; 1999; 14(6):493-501. PubMed ID: 10571947
[TBL] [Abstract][Full Text] [Related]
14. Mutant ion channel in cochlear hair cells causes deafness.
Trussell L
Proc Natl Acad Sci U S A; 2000 Apr; 97(8):3786-8. PubMed ID: 10760249
[No Abstract] [Full Text] [Related]
15. Differential expression of KCNQ4 in inner hair cells and sensory neurons is the basis of progressive high-frequency hearing loss.
Beisel KW; Rocha-Sanchez SM; Morris KA; Nie L; Feng F; Kachar B; Yamoah EN; Fritzsch B
J Neurosci; 2005 Oct; 25(40):9285-93. PubMed ID: 16207888
[TBL] [Abstract][Full Text] [Related]
16. A mutational hot spot in the KCNQ4 gene responsible for autosomal dominant hearing impairment.
Van Camp G; Coucke PJ; Akita J; Fransen E; Abe S; De Leenheer EM; Huygen PL; Cremers CW; Usami S
Hum Mutat; 2002 Jul; 20(1):15-9. PubMed ID: 12112653
[TBL] [Abstract][Full Text] [Related]
17. Functional coassembly of KCNQ4 with KCNE-beta- subunits in Xenopus oocytes.
Strutz-Seebohm N; Seebohm G; Fedorenko O; Baltaev R; Engel J; Knirsch M; Lang F
Cell Physiol Biochem; 2006; 18(1-3):57-66. PubMed ID: 16914890
[TBL] [Abstract][Full Text] [Related]
18. Degeneration of sensory outer hair cells following pharmacological blockade of cochlear KCNQ channels in the adult guinea pig.
Nouvian R; Ruel J; Wang J; Guitton MJ; Pujol R; Puel JL
Eur J Neurosci; 2003 Jun; 17(12):2553-62. PubMed ID: 12823462
[TBL] [Abstract][Full Text] [Related]
19. [KCNQ4 gene mutations affected a pedigree with autosomal dominant hereditary hearing loss].
Wang Q; Cao J; Li N; Yang Y; Wang Q; Yu L; Han D; Yang W
Zhonghua Er Bi Yan Hou Ke Za Zhi; 2002 Oct; 37(5):343-7. PubMed ID: 12772453
[TBL] [Abstract][Full Text] [Related]
20. DFNA2/KCNQ4 and its manifestations.
De Leenheer EM; Ensink RJ; Kunst HP; Marres HA; Talebizadeh Z; Declau F; Smith SD; Usami S; Van de Heyning PH; Van Camp G; Huygen PL; Cremers CW
Adv Otorhinolaryngol; 2002; 61():41-6. PubMed ID: 12408061
[No Abstract] [Full Text] [Related]
[Next] [New Search]
