203 related articles for article (PubMed ID: 35308122)
1. Failure Of Hearing Acquisition in Mice With Reduced Expression of Connexin 26 Correlates With the Abnormal Phasing of Apoptosis Relative to Autophagy and Defective ATP-Dependent Ca
Sun L; Gao D; Chen J; Hou S; Li Y; Huang Y; Mammano F; Chen J; Yang J
Front Cell Neurosci; 2022; 16():816079. PubMed ID: 35308122
[TBL] [Abstract][Full Text] [Related]
2. Autophagy precedes apoptosis during degeneration of the Kölliker's organ in the development of rat cochlea.
Hou S; Chen J; Yang J
Eur J Histochem; 2019 Jun; 63(2):. PubMed ID: 31189296
[TBL] [Abstract][Full Text] [Related]
3. Kölliker's organ-supporting cells and cochlear auditory development.
Chen J; Gao D; Sun L; Yang J
Front Mol Neurosci; 2022; 15():1031989. PubMed ID: 36304996
[TBL] [Abstract][Full Text] [Related]
4. Apoptosis pattern and alterations of expression of apoptosis-related factors of supporting cells in Kölliker's organ in vivo in early stage after birth in rats.
Liu J; Cai L; He Y; Yang J
Eur J Histochem; 2017 Aug; 61(3):2706. PubMed ID: 29046047
[TBL] [Abstract][Full Text] [Related]
5. Reduced postnatal expression of cochlear Connexin26 induces hearing loss and affects the developmental status of pillar cells in a dose-dependent manner.
Xie L; Chen S; Xu K; Cao HY; Du AN; Bai X; Sun Y; Kong WJ
Neurochem Int; 2019 Sep; 128():196-205. PubMed ID: 31034913
[TBL] [Abstract][Full Text] [Related]
6. Putative role of border cells in generating spontaneous morphological activity within Kölliker's organ.
Dayaratne MW; Vlajkovic SM; Lipski J; Thorne PR
Hear Res; 2015 Dec; 330(Pt A):90-7. PubMed ID: 26119178
[TBL] [Abstract][Full Text] [Related]
7. Cell degeneration is not a primary causer for Connexin26 (GJB2) deficiency associated hearing loss.
Liang C; Zhu Y; Zong L; Lu GJ; Zhao HB
Neurosci Lett; 2012 Oct; 528(1):36-41. PubMed ID: 22975134
[TBL] [Abstract][Full Text] [Related]
8. Deafness induced by Connexin 26 (GJB2) deficiency is not determined by endocochlear potential (EP) reduction but is associated with cochlear developmental disorders.
Chen J; Chen J; Zhu Y; Liang C; Zhao HB
Biochem Biophys Res Commun; 2014 May; 448(1):28-32. PubMed ID: 24732355
[TBL] [Abstract][Full Text] [Related]
9. The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice.
Schütz M; Scimemi P; Majumder P; De Siati RD; Crispino G; Rodriguez L; Bortolozzi M; Santarelli R; Seydel A; Sonntag S; Ingham N; Steel KP; Willecke K; Mammano F
Hum Mol Genet; 2010 Dec; 19(24):4759-73. PubMed ID: 20858605
[TBL] [Abstract][Full Text] [Related]
10. Kölliker's organ and the development of spontaneous activity in the auditory system: implications for hearing dysfunction.
Dayaratne MW; Vlajkovic SM; Lipski J; Thorne PR
Biomed Res Int; 2014; 2014():367939. PubMed ID: 25210710
[TBL] [Abstract][Full Text] [Related]
11. Timed conditional null of connexin26 in mice reveals temporary requirements of connexin26 in key cochlear developmental events before the onset of hearing.
Chang Q; Tang W; Kim Y; Lin X
Neurobiol Dis; 2015 Jan; 73():418-27. PubMed ID: 25251605
[TBL] [Abstract][Full Text] [Related]
12. A deafness mechanism of digenic Cx26 (GJB2) and Cx30 (GJB6) mutations: Reduction of endocochlear potential by impairment of heterogeneous gap junctional function in the cochlear lateral wall.
Mei L; Chen J; Zong L; Zhu Y; Liang C; Jones RO; Zhao HB
Neurobiol Dis; 2017 Dec; 108():195-203. PubMed ID: 28823936
[TBL] [Abstract][Full Text] [Related]
13. In Vitro Models of GJB2-Related Hearing Loss Recapitulate Ca
Fukunaga I; Fujimoto A; Hatakeyama K; Aoki T; Nishikawa A; Noda T; Minowa O; Kurebayashi N; Ikeda K; Kamiya K
Stem Cell Reports; 2016 Dec; 7(6):1023-1036. PubMed ID: 27840044
[TBL] [Abstract][Full Text] [Related]
14.
Beach R; Abitbol JM; Allman BL; Esseltine JL; Shao Q; Laird DW
Front Cell Dev Biol; 2020; 8():215. PubMed ID: 32300592
[No Abstract] [Full Text] [Related]
15. Mice with conditional deletion of Cx26 exhibit no vestibular phenotype despite secondary loss of Cx30 in the vestibular end organs.
Lee MY; Takada T; Takada Y; Kappy MD; Beyer LA; Swiderski DL; Godin AL; Brewer S; King WM; Raphael Y
Hear Res; 2015 Oct; 328():102-12. PubMed ID: 26232528
[TBL] [Abstract][Full Text] [Related]
16. [The function of Kölliker's organ in mammalian cochlear].
Hou SL; Yang J
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2017 Sep; 52(9):712-716. PubMed ID: 28910900
[TBL] [Abstract][Full Text] [Related]
17. Cellular and Deafness Mechanisms Underlying Connexin Mutation-Induced Hearing Loss - A Common Hereditary Deafness.
Wingard JC; Zhao HB
Front Cell Neurosci; 2015; 9():202. PubMed ID: 26074771
[TBL] [Abstract][Full Text] [Related]
18. Aberrant Cx26 hemichannels and keratitis-ichthyosis-deafness syndrome: insights into syndromic hearing loss.
Sanchez HA; Verselis VK
Front Cell Neurosci; 2014; 8():354. PubMed ID: 25386120
[TBL] [Abstract][Full Text] [Related]
19. Reduced Connexin26 in the Mature Cochlea Increases Susceptibility to Noise-Induced Hearing Lossin Mice.
Zhou XX; Chen S; Xie L; Ji YZ; Wu X; Wang WW; Yang Q; Yu JT; Sun Y; Lin X; Kong WJ
Int J Mol Sci; 2016 Feb; 17(3):301. PubMed ID: 26927086
[TBL] [Abstract][Full Text] [Related]
20. Assembly of the cochlear gap junction macromolecular complex requires connexin 26.
Kamiya K; Yum SW; Kurebayashi N; Muraki M; Ogawa K; Karasawa K; Miwa A; Guo X; Gotoh S; Sugitani Y; Yamanaka H; Ito-Kawashima S; Iizuka T; Sakurai T; Noda T; Minowa O; Ikeda K
J Clin Invest; 2014 Apr; 124(4):1598-607. PubMed ID: 24590285
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]