References
- Keller HE. Objective lenses for confocal microscopy. Pawley JB. Handbook of Biological Confocal Microscopy, 3rd. New York:Springer;2006.
- Egner A, Hell SW. Aberrations in confocal and multi-photon fluorescent microscopy induced by refractive index mismatch. Pawley JB. Handbook of Biological Confocal Microscopy, 3rd. New York:Springer;2006.
- Hell S, Reiner G, Cremer C, Stelzer EHK. Aberrations in confocal fluorescence microscopy induced by mismatches in refractive index. J Microsc. 1993;169:391–405.
- Hardie NA, MacDonald G, Rubel EW. A new method for imaging and 3D reconstruction of mammalian cochlea by fluorescent confocal microscopy. Brain Res. 2004;1000: 200–10.
- MacDonald GH, Rubel EW. Three-dimensional imaging of the intact mouse cochlea by fluorescent laser scanning confocal microscopy. Hear Res.2008;243:1–10.
- Spalteholz W. Über das Durchsichtigmachen von menschlichen und tierischen Präpareten und seine theoretischen Bedingungen. Leipizig: Hirzel; 1914.
- Voie AH, Burns DH, Spelman FA. Orthogonal-plane fluorescence optical sectioning: three-dimensional imaging of macroscopic biological specimens. J Microsc. 1993;170:229–36.
- Voie AH. Imaging the intact guinea pig tympanic bulla by orthogonal-plane fluorescence optical sectioning microscopy. Hear Res. 2002;171:119–28.
- Buytaert JAN, Dirckx JJJ. Design and quantitative resolution measurements of an optical virtual sectioning threedimensional imaging technique for biomedical specimens featuring two-micrometer slicing resolution. J Biomed Optics. 2007;12:014039.
- Buytaert JAN, Dirckx J. Tomographic imaging of macroscopic biomedical objects in high resolution and three dimensions using orthogonal-plane fluorescence optical sectioning. Appl Optics. 2009;48:941–8.
- Santi PA, Johnson SB, Hillenbrand M, GrandPre PZ, Glass TJ, Leger JR. Thin-sheet laser imaging microscopy for optical sectioning of thick tissues. BioTechniques. 2009;46:287–94.
- Hibbs AR, MacDonald G, Garsha K. Practical confocal microscopy. Pawley JB. Handbook of Biological Confocal Microscopy. 3rd. New York: Springer; 2006.
- Berlund AM, Ryugo DK. Neurofilament antibodies and spiral ganglion neurons of the mammalian cochlea. J Comp Neurol. 1991;306:393–408.
- Maison SF, Rosahl TW, Homanics GE, Liberman MC. Functional role of GABAergic innervation of the cochlea: phenotypic analysis of mice lacking GABAA receptor subunits α1, α2, α5, α6, β2, β3 or δ. J Neurosci. 2006;26:10315–26.
- Sato M, Henson MM, Henson OW, Smith DW. The innervation of outer hair cells: 3D reconstruction from TEM serial sections in the Japanese macaque. Hear Res. 1999;135:29–38.
- Berlund AM, Ryugo DK. Hair cell innervation by spiral ganglion neurons in the mouse. J Comp Neurol. 1987;255: 560–70.
- Oesterle EC, Campbell S. Supporting cell characteristics in long-deafened aged mouse ears. J Assoc Res Otolaryngol. 2009;10:525–44.
- Slepecky N, Ulfendahl M. Actin-binding and microtubule associated proteins in the organ of Corti. Hear Res.1992; 57:201–15.
- Maison SF, Adams JC, Liberman MC. Olivocochlear innervation in the mouse: immunocytochemical maps, crossed versus uncrossed contributions and transmitter colocalization. J Comp Neurol. 2003;455:406–16.
- Huang L-C, Thome PR, Housley GD, Montgomery JM. Spatiotemporal definition of neurite outgrowth, refinement and retraction in the developing mouse cochlea. Development. 2007;134:2925–33.