224 related articles for article (PubMed ID: 18093167)
1. Spatiotemporal loss of K+ transport proteins in the developing cochlear lateral wall of guinea pigs with hereditary deafness.
Jin Z; Ulfendahl M; Järlebark L
Eur J Neurosci; 2008 Jan; 27(1):145-54. PubMed ID: 18093167
[TBL] [Abstract][Full Text] [Related]
2. Malformation of stria vascularis in the developing inner ear of the German waltzing guinea pig.
Jin Z; Mannström P; Järlebark L; Ulfendahl M
Cell Tissue Res; 2007 May; 328(2):257-70. PubMed ID: 17252244
[TBL] [Abstract][Full Text] [Related]
3. Development of the stria vascularis and potassium regulation in the human fetal cochlea: Insights into hereditary sensorineural hearing loss.
Locher H; de Groot JC; van Iperen L; Huisman MA; Frijns JH; Chuva de Sousa Lopes SM
Dev Neurobiol; 2015 Nov; 75(11):1219-40. PubMed ID: 25663387
[TBL] [Abstract][Full Text] [Related]
4. Auditory function and cochlear morphology in the German waltzing guinea pig.
Jin Z; Mannström P; Skjönsberg A; Järlebark L; Ulfendahl M
Hear Res; 2006 Sep; 219(1-2):74-84. PubMed ID: 16870368
[TBL] [Abstract][Full Text] [Related]
5. Deafness in LIMP2-deficient mice due to early loss of the potassium channel KCNQ1/KCNE1 in marginal cells of the stria vascularis.
Knipper M; Claussen C; Rüttiger L; Zimmermann U; Lüllmann-Rauch R; Eskelinen EL; Schröder J; Schwake M; Saftig P
J Physiol; 2006 Oct; 576(Pt 1):73-86. PubMed ID: 16901941
[TBL] [Abstract][Full Text] [Related]
6. KCNK5 channels mostly expressed in cochlear outer sulcus cells are indispensable for hearing.
Cazals Y; Bévengut M; Zanella S; Brocard F; Barhanin J; Gestreau C
Nat Commun; 2015 Nov; 6():8780. PubMed ID: 26549439
[TBL] [Abstract][Full Text] [Related]
7. Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model.
Wangemann P; Itza EM; Albrecht B; Wu T; Jabba SV; Maganti RJ; Lee JH; Everett LA; Wall SM; Royaux IE; Green ED; Marcus DC
BMC Med; 2004 Aug; 2():30. PubMed ID: 15320950
[TBL] [Abstract][Full Text] [Related]
8. Potassium ion recycling pathway via gap junction systems in the mammalian cochlea and its interruption in hereditary nonsyndromic deafness.
Kikuchi T; Adams JC; Miyabe Y; So E; Kobayashi T
Med Electron Microsc; 2000; 33(2):51-6. PubMed ID: 11810458
[TBL] [Abstract][Full Text] [Related]
9. Expression of an inwardly rectifying K+ channel, Kir5.1, in specific types of fibrocytes in the cochlear lateral wall suggests its functional importance in the establishment of endocochlear potential.
Hibino H; Higashi-Shingai K; Fujita A; Iwai K; Ishii M; Kurachi Y
Eur J Neurosci; 2004 Jan; 19(1):76-84. PubMed ID: 14750965
[TBL] [Abstract][Full Text] [Related]
10. KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential.
Marcus DC; Wu T; Wangemann P; Kofuji P
Am J Physiol Cell Physiol; 2002 Feb; 282(2):C403-7. PubMed ID: 11788352
[TBL] [Abstract][Full Text] [Related]
11. Claudins in the tight junctions of stria vascularis marginal cells.
Florian P; Amasheh S; Lessidrensky M; Todt I; Bloedow A; Ernst A; Fromm M; Gitter AH
Biochem Biophys Res Commun; 2003 Apr; 304(1):5-10. PubMed ID: 12705875
[TBL] [Abstract][Full Text] [Related]
12. K+ cycling and the endocochlear potential.
Wangemann P
Hear Res; 2002 Mar; 165(1-2):1-9. PubMed ID: 12031509
[TBL] [Abstract][Full Text] [Related]
13. Long-lasting changes in the cochlear K+ recycling structures after acute energy failure.
Takiguchi Y; Sun GW; Ogawa K; Matsunaga T
Neurosci Res; 2013; 77(1-2):33-41. PubMed ID: 23827367
[TBL] [Abstract][Full Text] [Related]
14. Free radical stress-mediated loss of Kcnj10 protein expression in stria vascularis contributes to deafness in Pendred syndrome mouse model.
Singh R; Wangemann P
Am J Physiol Renal Physiol; 2008 Jan; 294(1):F139-48. PubMed ID: 17959752
[TBL] [Abstract][Full Text] [Related]
15. Deafness in Claudin 11-null mice reveals the critical contribution of basal cell tight junctions to stria vascularis function.
Gow A; Davies C; Southwood CM; Frolenkov G; Chrustowski M; Ng L; Yamauchi D; Marcus DC; Kachar B
J Neurosci; 2004 Aug; 24(32):7051-62. PubMed ID: 15306639
[TBL] [Abstract][Full Text] [Related]
16. Developmental expression and localization of KCNJ10 K+ channels in the guinea pig inner ear.
Jin Z; Wei D; Järlebark L
Neuroreport; 2006 Apr; 17(5):475-9. PubMed ID: 16543810
[TBL] [Abstract][Full Text] [Related]
17. Cellular localization of facilitated glucose transporter 1 (GLUT-1) in the cochlear stria vascularis: its possible contribution to the transcellular glucose pathway.
Ando M; Edamatsu M; Fukuizumi S; Takeuchi S
Cell Tissue Res; 2008 Mar; 331(3):763-9. PubMed ID: 18196278
[TBL] [Abstract][Full Text] [Related]
18. Progressive irreversible hearing loss is caused by stria vascularis degeneration in an Slc26a4-insufficient mouse model of large vestibular aqueduct syndrome.
Ito T; Nishio A; Wangemann P; Griffith AJ
Neuroscience; 2015 Dec; 310():188-97. PubMed ID: 26363152
[TBL] [Abstract][Full Text] [Related]
19. Na-K-Cl cotransporter expression in the developing and senescent gerbil cochlea.
Sakaguchi N; Crouch JJ; Lytle C; Schulte BA
Hear Res; 1998 Apr; 118(1-2):114-22. PubMed ID: 9606066
[TBL] [Abstract][Full Text] [Related]
20. Immunolocalization of ClC-K chloride channel in strial marginal cells and vestibular dark cells.
Sage CL; Marcus DC
Hear Res; 2001 Oct; 160(1-2):1-9. PubMed ID: 11591484
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]