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Items: 1 to 20 of 111


Connexin30 deficiency causes instrastrial fluid-blood barrier disruption within the cochlear stria vascularis.

Cohen-Salmon M, Regnault B, Cayet N, Caille D, Demuth K, Hardelin JP, Janel N, Meda P, Petit C.

Proc Natl Acad Sci U S A. 2007 Apr 10;104(15):6229-34. Epub 2007 Mar 30.


Compartmentalization established by claudin-11-based tight junctions in stria vascularis is required for hearing through generation of endocochlear potential.

Kitajiri S, Miyamoto T, Mineharu A, Sonoda N, Furuse K, Hata M, Sasaki H, Mori Y, Kubota T, Ito J, Furuse M, Tsukita S.

J Cell Sci. 2004 Oct 1;117(Pt 21):5087-96.


Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential.

Teubner B, Michel V, Pesch J, Lautermann J, Cohen-Salmon M, Söhl G, Jahnke K, Winterhager E, Herberhold C, Hardelin JP, Petit C, Willecke K.

Hum Mol Genet. 2003 Jan 1;12(1):13-21.


Absence of strial melanin coincides with age-associated marginal cell loss and endocochlear potential decline.

Ohlemiller KK, Rice ME, Lett JM, Gagnon PM.

Hear Res. 2009 Mar;249(1-2):1-14. doi: 10.1016/j.heares.2008.12.005. Epub 2008 Dec 25.


Cellular characterization of Connexin26 and Connnexin30 expression in the cochlear lateral wall.

Liu YP, Zhao HB.

Cell Tissue Res. 2008 Sep;333(3):395-403. doi: 10.1007/s00441-008-0641-5. Epub 2008 Jun 26.


The endocochlear potential depends on two K+ diffusion potentials and an electrical barrier in the stria vascularis of the inner ear.

Nin F, Hibino H, Doi K, Suzuki T, Hisa Y, Kurachi Y.

Proc Natl Acad Sci U S A. 2008 Feb 5;105(5):1751-6. doi: 10.1073/pnas.0711463105. Epub 2008 Jan 24.


Impaired stria vascularis integrity upon loss of E-cadherin in basal cells.

Trowe MO, Maier H, Petry M, Schweizer M, Schuster-Gossler K, Kispert A.

Dev Biol. 2011 Nov 1;359(1):95-107. doi: 10.1016/j.ydbio.2011.08.030. Epub 2011 Sep 9.


Gastric type H+,K+-ATPase in the cochlear lateral wall is critically involved in formation of the endocochlear potential.

Shibata T, Hibino H, Doi K, Suzuki T, Hisa Y, Kurachi Y.

Am J Physiol Cell Physiol. 2006 Nov;291(5):C1038-48. Epub 2006 Jul 5.


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.


Deficiency of transcription factor Brn4 disrupts cochlear gap junction plaques in a model of DFN3 non-syndromic deafness.

Kidokoro Y, Karasawa K, Minowa O, Sugitani Y, Noda T, Ikeda K, Kamiya K.

PLoS One. 2014 Sep 26;9(9):e108216. doi: 10.1371/journal.pone.0108216. eCollection 2014.


Connexin30 null and conditional connexin26 null mice display distinct pattern and time course of cellular degeneration in the cochlea.

Sun Y, Tang W, Chang Q, Wang Y, Kong W, Lin X.

J Comp Neurol. 2009 Oct 20;516(6):569-79. doi: 10.1002/cne.22117.


Perivascular macrophage-like melanocyte responsiveness to acoustic trauma--a salient feature of strial barrier associated hearing loss.

Zhang F, Dai M, Neng L, Zhang JH, Zhi Z, Fridberger A, Shi X.

FASEB J. 2013 Sep;27(9):3730-40. doi: 10.1096/fj.13-232892. Epub 2013 May 31.


Reduction in the endocochlear potential caused by Cs(+) in the perilymph can be explained by the five-compartment model of the stria vascularis.

Kakigi A, Takeuchi S, Ando M, Higashiyama K, Azuma H, Sato T, Takeda T.

Hear Res. 2002 Apr;166(1-2):54-61.


Alström Syndrome protein ALMS1 localizes to basal bodies of cochlear hair cells and regulates cilium-dependent planar cell polarity.

Jagger D, Collin G, Kelly J, Towers E, Nevill G, Longo-Guess C, Benson J, Halsey K, Dolan D, Marshall J, Naggert J, Forge A.

Hum Mol Genet. 2011 Feb 1;20(3):466-81. doi: 10.1093/hmg/ddq493. Epub 2010 Nov 11.


Effects of mutations at the W locus (c-kit) on inner ear pigmentation and function in the mouse.

Cable J, Huszar D, Jaenisch R, Steel KP.

Pigment Cell Res. 1994 Feb;7(1):17-32.


How is the highly positive endocochlear potential formed? The specific architecture of the stria vascularis and the roles of the ion-transport apparatus.

Hibino H, Nin F, Tsuzuki C, Kurachi Y.

Pflugers Arch. 2010 Mar;459(4):521-33. doi: 10.1007/s00424-009-0754-z. Epub 2009 Dec 11. Review.


Spinster homolog 2 (spns2) deficiency causes early onset progressive hearing loss.

Chen J, Ingham N, Kelly J, Jadeja S, Goulding D, Pass J, Mahajan VB, Tsang SH, Nijnik A, Jackson IJ, White JK, Forge A, Jagger D, Steel KP.

PLoS Genet. 2014 Oct 30;10(10):e1004688. doi: 10.1371/journal.pgen.1004688. eCollection 2014 Oct.


Functional and morphological response of the stria vascularis following a sensorineural hearing loss.

Hellier WP, Wagstaff SA, O'Leary SJ, Shepherd RK.

Hear Res. 2002 Oct;172(1-2):127-36.

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