References
- Tasaki I, Spyropoulos CS. Stria vascularis as source of endocochlear potential. J Neurophysiol 1959; 22: 149–55
- Narcus DC. Nonsensory electrophysiology of the cochlea: stria vascularis. Neurobiology of hearing: the cochlea., RA Altschuler, et al. Raven Press, NY 1986; 123–37
- Offner F F, Dallos P, Cheatham MA. Positive endocochlear potential: mechanism of production by marginal cells of stria vascularis. Hear Res 1987; 29: 117–24
- Lim D J, Flock A. Scanning Electron Microscope Specimen Preparation Technique For Dissociated Strial Marginal Cells. Scanning Electron Microsc 1984; 3: 1407–11
- Rarey K E, Patterson K. Establishment of inner ear epithelial cell culture: isolation, growth and characterization. Hear Res 1989; 38: 277–88
- Achouche J, Wu A H, Tran Ba Huy P. Primary culture of strial marginal cells of guinea pig: growth, morphologic features, and characterization. Ann Otol Rhinol Laryngol 1991; 100: 999–1006
- Melichar I, Gitter AH. Primary culture of vital marginal cells from cochlear explants of the stria vascularis. Eur Arch Otol Rhinol Laryngol 1991; 248: 358–65
- Melichar I, Gitter AH. Ultrastructure of cultured marginal cells of the guinea pig cochlea. Acta Otolaryngol (Stockh) 1992; 112: 762–6
- Liu D S, Achouche J, Wu A H, Trotier D, Tran Ba Huy P. Luminal non-specific cationic channels in cultured strial marginal cells of guinea pig and gerbil as determined by patch clamp technique. Acta Otolaryngol (Stockh) 1991; 111: 298–303
- Gitter A H, Ikeda M, Zenner HP. The resting potential of marginal cells in stria vascularis explants. Eur Arch Otorhinolaryngol 1991; 248: 492–4
- Martin F, Marianowski R, Tu T-Y, Herman P, Tran Ba Huy P. Modulation of cyclic AMP production by strial marginal cells from gerbil in culture. Hear Res 1994; 81: 33–41
- Lucchesi P A, Sweadner KJ. Postnatal changes in Na, K-ATPase isoform expression in rat cardiac ventricle. J Biol Chem 1991; 266: 9327–31
- Zuo J, Curtis L M, Yao X, ten Cate W JF, Rarey KE. Expression of Na, K-ATPase α and β isoforms in the neonatal rat cochlea. Acta Otolaryngol (Stockh) 1995; 115: 497–503
- Kobayashi T, Okada T, Sequchi H. Cerium-based cyto-chemical method for detection of ouabain-sensitive, potassium-dependent, p-nitrophenylphosphatase activity at physiological pH. J Histochem Cytochem 1987; 35: 601–11
- Kanoh N. Dopamine inhibits the Na-K ATPase activity of the stria vascularis in the cochlea. Acta Otolaryngol (Stockh) 1995; 115: 27–30
- ten Cate WJ-F, Curtis L M, Rarey KE. Na, K- ATPase a and β subunit isoform distribution in the rat cochlear and vestibular tissues. Hear Res 1994; 75: 151–60
- Ryan A F, Watts AG. Expression of mRNAs encoding α and β subunit isoforms of the Na, K-ATPase in the rat cochlea. Mol Cell Neurosci 1991; 2: 179–87
- Skou JC. Enzymatic basis for active transport of N+ and K+ across cell membrane. Physiol Rev 1965; 45: 596–617
- Whittam R. Wheeler KP. Transport across cell membrane. Ann Rev Physiol 1970; 32: 21–60
- Ernst SA. Transport adenosine triphosphatase cytochemistry. II. Cytochemical localization of ouabain-senisitive, potassium-dependent phosphatase activity in the secretory epithelium of the avian salt gland. J Histochem cytochem 1972; 20: 23
- Mayahara H. Ogawa K. Ultracytochemical localization of ouabain-sensitive potassium-dependent p-nitro-phenyl phosphatase activity in the rat kidney. Acta Histochem Cytochem 1980; 13: 90